Thesis 1992 Zhang
Thesis 1992 Zhang
UNIVERSITY OF TECHNOLOGY
LIBRARY
AUTHOR/FILING TITLE
AtZ.C.H \ \I ..cs
~
f~R h£FER£NCf ~NLY
11NO : ON3143::f3U ,~tH
(~V~;;;;;.;;~
:~~ -
111111
---- 11111
...~.
/
/
Crossflow MicrofiItration Modelling
by
Guan Mei Zhang B Se
A DOCTORAL THESIS
December 1992
-- ----~~I
(N:uo71,S-'i?
- -- - ...... _ .... _---
~
Dedicated To
Crossflow microfiltration membrane fouling and the deposition of solids onto the
filter surface have been investigated using a process fluid (seawater), latex and a ground
mineral. The performance of various membrane materials has also been studied,
including: acrylonitrile, polypropylene, PTFE, ceramic and stainless steel. The seawater
filtration work showed in Chapter 3 that good filtrate flux rates can be maintained if
material fouling or depositing on the membrane can be prevented from entering the
membrane structure. A surface deposit may be removed by mechanical means such as
backflushing with permeate or compressed air. This aspect of the work indicated that
a more comprehensive study of fouling was required. Existing crossflow filtration
membrane models did not adequately represent even the simplest filtration when
penetration of the membrane structure applied. Such conditions occurred during latex
filtration in Chapter 4.
Latex of varying sizes and density were manufactured and filtrations using
acrylonitrile membranes were performed. Considerable deposition of latex inside the
membrane pores occurred despite the nominal rating of the membrane being less than
the latex particle diameter. Thus the membranes relied on a depth filtration mechanism
rather than a surface straining mechanism for filtration effectiveness. A standard
filtration blocking model was modified for use in crossflow microfiltration, coupled
with a mass balance on the amount of material filtered. This mathematical model was
then used to predict and correlate the rate of filtration flux decay with respect to filtration
time during crossflow filtration. The model provided acceptable accuracy and is an
improvement on existing empirical models for the flux decay period.
Thanks are also due to Mr. M R Kerry, Mr. S G Graver and Mr. G P Moody for
the particle analysis; Mr. R G Boyden, Mr. F Page and Mr. J S Bates forthe photographs;
Dr. Y Z Lu, Mr. I Sinclair, Mr. T M Neale and Miss. A M Braithwaite for the computer
and electronics work; Mr. L Moore, Mr. M J Amos, Mr. A R Eyre, and Mr. J B Powell
for the mechanical work; Mr. J Wang and Mr. A Milne for their help in producing
latex suspensions.
Further, I should also like to pay my tribute to all the staff of Chemical Engineering
for their help, advice and friendship.
ABSTRACT
ACKNOWLEDGEMENTS
1 Introduction 1
1.1 Microfiltration (MF), Ultrafiltration (UF)
and Reverse Osmosis (RO) 2
1.2 History 4
1.2.1 Early history 5
1.2.2 Development in later years 5
1.2.3 MF in the 1980s 7
1.2.4 Aspects of MF literature 7
1.3 Membranes 8
1.3.1 Requirements 8
1.3.2 Types 8
1.3.3 Characteristics 13
1.4 Membrane configurations 15
1.4.1 Tubular 15
1.4.2 Hollow fibres 16
1.4.3 Spiral-wound 16
1.4.4 Flat 16
1.4.5 Pleated 19
1.5 Operation systems 19
1.5.1 Single-pass and cascade 20
1.5.2 Batch 21
1.5.3 Continuous 22
1.6 Applications 23
1.6.1 Laboratory tests and medical analysis 23
1.6.2 Effluent treatment 24
1.6.3 Food industries 25
1.6.4 Engineering processes 26
1.6.5 Pharmaceutical and biochemical industries 26
1.7 Permeate flux rate decline and prevention techniques, 27
1.7.1 Resistances to the permeate flow 27
I
1.7.2 Membrane fouling mechanisms 28
1.7.3 Adhesive and removal forces 30
1.7.4 Techniques to prevent the flux rate decline 31
11
3.3 Experiments with Nonh Sea seawater 104
3.3.1 Test rig and control programs 104
3.3.2 Test items 107
3.3.3 Test procedures 107
3.3.4 Test results and discussions 107
3.4 Brief summary 109
III
---- ---
NOMENCLATURE
REFERENCES
IV
FIGURES
Fig 1 The place for MP, UF and RO as separation processes
[Osmotic Inc., 1985] 3
Fig 2 The configurations of crossflow and dead-end filtration 4
Fig 3 Sharp & diffusive cutoff vs. retention efficiency 15
Fig 4 Me~brane configurations 17
Fig 5 Dead-end filtration cells 19
Fig 6 Basic operating diagram 20
Fig 7 Single-pass and cascade system 21
Fig 8 Batch system 22
Fig 9 Continuous system 22
Fig 10 Resistances to the filtration 28
Fig 11 Two filtration models 35
Fig 12 The schematic diagram of "Three-Zone" model. 46
Fig 13 The interaction between turbulent burst and particles 67
Fig 14 Layout of laboratory test rig 76
Fig 15 Size distribution of solids in seawater and silica 79
Fig 16 Size distribution of seawater algae in cleaned tap water 80
Fig 17 Shedding effect of the rig at 25 Vrnin 84
Fig 18 Shedding effect of the rig at 12.5 Vrnin 84
Fig 19 Flux rate of PTFE and ceramic membranes with tap water 88
Fig 20 Flux rate with clean water (Fairey and Enka) 88
Fig 21 Water flux rate of ceramic filter 90
Fig 22a Flux rates of metal membranes (Re 8500) 91
Fig 22b Flux rates of metal membranes (Re 42500) 91
Fig 23 Flux rate of clean water (Versapor) 92
Fig 24a Permeate flux rate at 5 mg/l of lipid 93
Fig 24b Permeate flux rate at 10 mg/l of lipid 94
Fig 24c Permeate flux rate at 20 mg/l of lipid 94
Fig 25 Flux rate of Enka filter at different concentrations 96
Fig 26a Flux rate of ceramic filter at low pressure 97
Fig 26b Flux rate of ceramic filter at high pressure 97
Fig 27 Flux rate of Versapor membrane at high pressure 98
Fig 28 Flux rate of algae on metal membrane 99
v
Fig 29 Flux rate of algae on polymer membrane 99
Fig 30 Polymer membrane 102
Fig 31 Metal fibre membrane 103
Fig 32 Layout of seawater filtration rig 105
Fig 33 Flux rate for different filters 108
Fig 34 Flux rate of ceramic filters over several days 108
Fig 35 Flux rate of metal filters with or without precoating 109
VI
transmembrane pressure 147
Fig 52 Mathematical analysis of test 04 149/50
Fig 53 Comparisons of measured and predicted permeate flux rate 159/62
Fig 54 The layout of test rig 168
Fig 55 The configuration of filter module 168
Fig 56 Endcaps of tangential and normal modules 169
Fig 57 The side view of the filter with helically wound o-ring 170
Fig 58 Inlet pressure (PI) as a function of feed flow rate
for different endcap types 171
Fig 59 Pressure inside the membrane module (P3) and downstream
of the filter (P2) for different endcap types 172
Fig 60 Permeate flux rate decay with time and the effect of
variable temperature 173
Fig 61 Particle size distributions of fine and coarse powders 174
Fig 62 Cumulative permeate volume with time and use of
initial rate for membrane resistance 176
Fig 63a Equilibrium permeate flux rate with pressure using
different endcaps (1.5% coarse powder) 183
Fig 63b Equilibrium permeate flux rate with pressure using
different endcaps (1.6% fine powder) 183
Fig 64a Equilibrium permeate flux rate with pressure using
different endcaps (4% coarse powder) 184
Fig 64b Equilibrium permeate flux rate with pressure using
different endcaps (3% fine powder) 184
Fig 65a Equilibrium permeate flux rate with pressure at various
crossflow velocities using normal endcaps
(coarse powder) 185
Fig 65b Equilibrium permeate flux rate with pressure at various
crossflow velocities using normal endcaps
(fine powder) 185
Fig 66a Equilibrium permeate flux rate with pressure at various
crossflow velocities using tangential endcaps
(coarse powder) 186
Fig 66b Equilibrium permeate flux rate with pressure at various
cross flow velocities using tangential endcaps
VII
(fine powder) 186
Fig 67 Schematic diagram of particles in stationary orbit
around filter due to balance of centrifugal
field and liquid drag force 187
Fig 68a Permeate flux rate with tangential endcaps at different
particle sizes (1.5 %) 191
Fig 68b Permeate flux rate with tangential endcaps at different
particle sizes (3 %) 191
Fig 69 The deposits on the filter with different endcaps 192
Fig 70a Equilibrium flux rate as a function of power requirement
(1.5% coarse powder) 195
Fig 70b Equilibrium flux rate as a function of power requirement
(1.6% fine podwer) 195
Fig 71a Equilibrium flux rate as a function of power requirement
(3% coarse powder) 196
Fig 71b Equilibrium flux rate as a function of power requirement
(4% fine powder) 196
VIII
TABLES
Table 1 Early history of membrane research 5
Table 2 Commercial developments of MF 6
Table 3 Comparison of configurations 18
IX
APPENDICES
Appendix 1 Photographs of microfiltration membranes
x
Chapter 1 1
CHAPTER 1
Introduction
from that of the liquid; one had a helical channel around the filter, and the other had
tangential endcaps. The centrifugal force produced by the spinning flow around the
filter retarded the approach of particles towards the membrane surface so that particle
deposition was reduced. The results also showed that the filter with tangential endcaps
could save as much as 20 % of the energy compared to the conventional one.
Conclusions and the recommendations for the further work are put forward in
Chapter 6.
which the membrane plays the role of a material boundary to control the transport of
matter across it - it remains impermeable to a specific substance or groups of substances
depending on the properties and working conditions of the system. The other two
pressure-driven membrane separation processes are Reverse Osmosis (RO) and Ultra-
filtration (UF).
All these processes are attractive for industries due to their following
adv.antages [Cartright, 1991):
Continuous process - resulting in automatic and uninterrupted operation.
Low energy consumption - involving neither phase nor temperature changes.
Modular design - no significant size limitations.
Maintenance - minimum of moving parts with low maintenance requirements.
Efficiency - discrete membrane barrier to ensure clear separation;
Purity - no chemical additions required.
The distinctions between these three processes are quite arbitrary, the operating
principles are similar and applications overlap. Some differences are, however, clear
and these will be discussed in the following sub-sections:
1) Separation range
They can be distinguished by the size of the particles or molecules retained by
the membranes, so that each process can be defined by the rated pore size shown in Fig
1, in which RO is less than 0.001 Ilm, UP is 0.001 - 0.1 Ilm, MP is 0.1 - 20 Ilm.
These figures are used here only for the purpose of illustrating the range of membrane
Chapter 1 3
separation processes. Some authors have different definitions for the range of micro-
,
filtration, e.g. 0.02 - 14 J.1m [Bal10w & Porter, 1980], 0.05 - 20 J.1m [Porter & Billiet,
1986], 0.01 - 10 J.1m [Boonthanon et al, 1991], and 0.1 - 10 J.1m [Cartwright, 1991]
etc.
2) Solubility
MF can only separate suspended particles (pollen, starch, DNA, bacteria),
UF can separate macromolecules (protein, red blood cells) as well as particles, whereas
RO can separate small molecules and ions.
Separation I BO I Particle
I MF I
process I UF I filtration
4) Operating pressure
RO needs a high hydraulic pressure (20 - 1()() Bar) to overcome osmotic
pressure; whereas MP and UF work under lower pressure (0.1 - 10 Bar) because the
macromolecules solutes and colloidal species in these two processes usually have
insignificant osmotic pressures.
Feed
Feed
... ++
• •••• • ••••
•••••
•••• I membrane
•••••••
• • I
+ +
+Permeate + + +
Permeate
(a) CrossfJow (b) Dead-end
Fig 2 The configurations of crossflow and dead-end filtration
5) Separation mechanisms
The mechanism of MP and UF is "sieving" and "sorption", the permeate
selecting process is pore-suspended species interaction, the permeate flow is viscous
type, whereas the permeate selecting process in RO is membrane material-permeate
interaction, the permeate flow is diffusive.
6) Chemical property
MP changes none of the chemical properties of the fluid whereas in UF and
RO, separation of the dissolved species modifies the chemical potential and creates a
gradient which tends to make the separated solvent diffuse back in the reverse direction.
1.2 History
As a process, membrane separation is as old as any living organism; as a
subject, it has been studied for hundreds of years; however, as a practical technique,
it is new and has a history of only 30 years; as a science, there is still more to explore.
Chapter 1 5
semi-commercial scale and the product was named "membrane-filter". This kind of
filter was fIrst produced on a small commercial scale by Sartorius-Werkes in 1927 and
found its application in laboratory research work.
Table 2
Commercial developments of MF
1918 Zsigmondy & Bachmann Developed commercial process
1927 Sartorius-Werkes Began commercial production
1947 Mueller Membrane filter method for culturing bacteria [Mueller, 1947a]
1950 GoeLZ Improved production method and grid-marked membrane
[GoeLZ, 1947 & 1951]
1952 Lovell Chemical Co Designed and constructed large scale equipments production
1954 Millipore Corp First membrane company formed
1962 Gelman Instrument Co Cellulose tri-acetate membrane
1962 Sartorius Co Regenerated cellulose membrane
1963 Millipore, Gelmann, PVC and nylon membranes
Sartorius, S & S
1963 Fleischer, Price & Walker(G.E.) Track-etch membrane [Feischer et alI963,1964 & 1969]
1964 Gelman Sciences Fabric reinforced membrane
1964 Selas Florronics Silver membrane [Minneci & Pauison, 1988]
1970 Celanese Polypropylene membrane [Druin et ai, 1974]
1970 GoreCorp PTFE membrane [Gore, 1976a & 1976b]
1975 Hydronautics & Membrane Thermal-inversion process
1979 Gelman Polysulfone
1980 Millipore Polyvinylidene fluoride
1981 NucJepore Polyester
1984 Norton Co., Ceraver Alumina
In the early 1950s, membranes began to be recognized for their value and
commercial potential through the use of microfiltration for air monitoring, laboratory
analysis, and diagnosis testing. Several European and USA companies were formed
in the mid 1950s and early 1960s to explore the above technologies and for other filtration
industries including UF for dialysis and RO for desalination.
Chapter 1 7
Activities were accelerated in the mid 1960s and early 1970s, MP was applied
for parenteral drug filtration for injectable substances, manufacturing particle- and
bacteria-free rinsing water for the semiconductor industry, and medical devices such
as intravenous filters and spike vents.
1.3 Membranes
1.3.1 Requirements
Since the membrane is the key element of a microfiltration process, it must
have:
- high hydraulic permeability to liquid (water) and high retention efficiency to
panicles;
- good mechanical durability, chemical and thermal stability as well as
relatively long lifespan;
- ease of restoration of the initial permeability after cleaning/sanitizing;
- low cost and large scale for manufacture.
1.3.2 Types
The MP membranes can be catalogued into three groups by their nature: natural
(biological), polymeric (organic) and mineral (inorganic).
a) Natural
Animal membranes (e.g. pig and fish bladders) were the first ever used isotopic
. membranes [Michael, 1968]. Because of their poor performances and limited sources,
they are not used for MP nowadays.
Fabric materials have been used for filtration for a long time, and still are
[Dahlheimer et ai, 1970; Hunt et ai, 1987a, 1987b].
Chapter 1 9
Metal material should be soned into this group, however, due to their costs
and manufacturing processes, they are listed in the mineral group.
b) Polymeric
The first polymer membrane was commercialized by Zigmondy & Bachmann
in Germany in 1918. It was a nitrocellulose film based on the solution cast method.
There are many different membranes today based on different synthetic
processes. Some membranes manufactured by these processes are shown in Fig 1 of
Appendix 1 respectively.
They can be either hydrophilic or hydrophobic, and the forms can be tubular,
sheet or hollow fibres or pleated into any cartridge, they are usually 100 ~m thick, and
become 3 - 8 mm thick when supponed by a felt of non woven cloth [Le & Ward, 1984]
or a weft [Schiele & Alt, 1978; Knibbs, 1981; Tanny et ai, 1982]. The pore size
can be rated as low as 0.2 ~m.
This is the oldest and most common method, however, the membranes by
this method have about 90% of the membrane market share.
Chapter 1 10
2) Stretch method
This is the second most common method for manufacturing MF membranes
with about 10% of the polymer membrane market share.
It is based on stretching a polymer film such as polypropylene (Celgard) or
Teflon - polytetrafluorethylene (PTFE) (Goretex) [Brock, 1983] to form the pores.
They are 1-2 mm thick and hydrophobic, but wettable by applying'surfactants.,
The pore size can be as low as 0.1 Ilm
3) Thermoplast method
These membranes consist of more or less graded powders. The grains are
either fixed by heating or bonded by porogenic agents [Rivet, 1979]. The materials for
this method are polyvinylchloride (PVC), polythylene, polystyrene and polymids.
5) High-speed method
The so called Sunbeam process creates membranes by crosslinking monomers
and oligomers under either an ultraviolet or electron-beam source. The membranes may
be either hydrophilic or hydrophobic, 2 - 4 mm in thickness when supported by
nonwoven fabric materials [Tanny, 1986]
The main advantage of this process is that it can yield 1.5 - 2.4 m wide webs
at 105 - 180 mlmin speed comparing to the conventional process which usually works
at 1.5 - 4.5 mlmin for 0.3 - 0.9 m wide webs.
------- - - ------------------
Chapter 1 11
6) Sintering method
PTFE may be sintered like metal to obtain hydrophobic membranes with an
absolute rating of 0.1 I1m [Societe Beige de Filtration, 1975).
7) Laser method
This new method was developed in the late 1980s for manufacturing
membranes. The membrane is comprised of a flat foil of polymers, with cylindrical
or funnel-shaped pores formed by pulsed laser beams. The pores are perfectly round
and their positions, density (numbers in unit area) can be controlled by the laser.
[Flottmann & Trezel, 1990).
This membrane can improve separation by particle size, resistance to blinding,
and the rate of permeate flux.
8) Composite method
When two microporous films are layered together, the resulting pore size
distribution will be narrower. The pore size may be as low as O.Oll1m which is already
the lowest limit of MF by any definition [Steadly & Laccetti, 1988).
c) Mineral
The first filtration equipment with mineral materials was nothing but a cracked
jar [Mason, 1991). However, it was the late 1950s when the synthetic mineral
membranes were originally developed by Oak Ridge National Laboratory in USA and
CEA in France. In the early 1960s, a nickel membrane was made by plating nickel
on nickel wire mesh with pore sizes 0.05 to 0.3 I1m. The first commercial mineral
membrane was a silver one by Selas F1otronics in 1964 based on the similar process.
The real application of mineral membranes started in the early 1980s as a result of new
powder metallurgy. Their emergence has greatly increased the potentials of MF in
industries due to their unique features:
- Thermal stability
- Mechanical stability
- Chemical resistance
- Controlled, defined, stable pore structure
- Microbiological resistance
- Backflush capability
- Reduced fouling/flux loss
Chapter 1 12
- High throughput/volume.
The commercial mineral membranes can be roughly divided into three groups:
ceramic, metal and composite. Some ceramic membranes are shown in Fig 2 and metal
membranes in Fig 3 respectively in Appendix 1.
1) Ceramic
The ceramic membranes can be made by sintering method. They are formed
by the use of layers of different particle sizes. The smaller the pore size, the thinner
the layer. The matrix is a few hundredths of a micron thick and consists of grains of
some tenths of a micron. A layer of some tenths of a micron with even finer grains is
then deposited on the matrix surface to obtain the desired absolute ratings. The details
of the process can be obtained in the paper presented by Charpin et al (1988) and its
references 15-18.
The materials can be metal oxides, nitrides, and carbides, e.g. u-AI 20 3,
'Y-AI203 [Hsieh et aI, 1988], glass (90% Si02)[Ogasawani et aI, 1991], silicon carbide
(SiC) [Charpin et aI, 1988].
Most of the ceramic membranes are asymmetric in structure and have a porosity
of 50%. They are excellent in chemical, thermal and mechanical properties, and used
in tubular or monolithic multichannel modules, it was recently reported that ceramic
membranes in sheet form had been commercially manufactured [Cowieson, 1992].
The disadvantages include small-scale production and higher costs than polymeric
membranes.
2) Metal
Porous metals for metal membranes are available in a variety of forms including
sintered powders, wire mesh, sintered mesh, sintered fibres, and photo etched screens.
The porosity is also about 50% and pore size can be 1 ~m. They can be operated with
the help of electric or magnetic fields to enhance particle rejection ability.
The materials may be stainless steel by sintering; silver by plating [Druin et
al, 1974], or by temperature induced phase separation [Minneci & Paulson, 1988], or
by electron or ion irradiation [Japanese Patent Application, 1986]; aluminium by
double-sided etching [Bailey, 1991], copper, metal fibres and sintered metal fibres
Chapter I 13
3) Composite
Most ceramic membranes are composed with several layers different grain
size. However, mineral membranes can be funher made into composite with itself
or another material by sintering, e.g zirconia on inconel 600 [Davidson et al, 1990],
carbon on sintered metals [Boudier, 1990]. The resulting membranes have a better
mechanical durability than the ceramic membranes.
1.3.3 Characteristics
a) Permeate rate
Permeate rate (or flux rate) is pressure dependent but often less so than in RO,
it also normally increases with increasing feed flow rate and temperature, decreases
with concentration and with operating time until a force balance is set up on the membrane
surface. The mechanism for this will be discussed in the following chapter.
b) Surface charge
Most MF membranes are negatively charged, however, some membranes
like fibrous asbestos can be made into positively charged in order to increase its retention
efficiency [Blosse, 1982]. A type of charged membrane has been reponed in the
manufacture of ultrapure water [Yasminov et al, 1990].
c) Lifespan
Membrane life normally decreases with increasing temperature and depends
on the time-temperature condition of exposure to cleaning/sanitizing methods.
applications, the asymmetric membranes are used in a reverse way as those in RO and
UF: the opening side faces the feed flow to work as an inherent prefilter for the
membranes.
f) Retention efficiency
1) Porous filter
Most MF membranes have a "nominal" retention efficiency due to the broad
pore size distribution - some pores are even several times as large as the rated values so
that they can only retain some percentage (e.g. 90%, 95%, 98%) of all particles which
are equal to the rating of the membrane. Furthermore, the retention efficiency depends
on the depth and tortuosity of the matrix which also trap a number of particles below
the rated pore size. By this means, these membranes have a "diffusive cutoff' char-
acteristic. The membranes are catalogued by some authors as "porous media filter".
2) Screen filter
The membranes made by etching or laser method have unique pore size and
therefore their retention efficiency is "absolute". They can retain as high as 99.9999%
of the particles equal to or larger than their pore ratings. So that they have a "sharp
cutoff' and catalogued as "screen filter"
The relationship between the retention efficiency and different "cutoff's is
schematically shown in Fig 3.
However, the above definitions are nominal since there are other factors which
determine the retentivity, e.g. the size, shape, charge and deformability of the particles,
and therefore, the flake or linear flexible particles are less prone to clog the pores than
the shephrical hard particles with the same nominal size. Fluid shear stress near the
pores, electrostatic forces, van der Waals force, pH values of the fluid and the dynamic
membrane formed from particles or solutes will also affect the retentivity.
The retention is largely pressure independent for incompressible deposited
film or cake, but somewhat sensitive to flow rate.
Chapter I IS
100
Diffusive cutoff
Sharp cutoff
o
Particle size (microns)
Fig 3 Sharp & diffusive cutoff vs. retention efficiency
Chapter 1 16
Tubular membrane is the simplest form, they are not prone to blockage, easy
to clean chemically and physically, and easily removed or replaced. Its disadvantages
are large space for installation of a given membrane area, the high "hold-up" volume,
difficult to check leakage if in bundles and relatively high energy costs for pumping.
1.4.3 Spiral-wound
Two rectangular flat membranes are placed one on the top of the other,
separated by a porous material, and sealed together on three sides. The fourth side is
separately sealed along the length of a tube perforated to form a header for removing
the permeate which passes through the membranes from the outside. A spacer is laid
on the top of the two membranes which are then rolled round the header tube to form
the spiral. The spiral is sealed into a cylindrical housing and the process fluid is fed
from one end to the other through the region occupied by the spacer and across the
membrane surface. Permeate will enter the porous membrane interspace and spiral
round to the header. The flow through the module is basically laminar although a degree
of turbulence is promoted by the spacers. (Fig 4c)
They are cheap, very compact and have low pumping costs, but are easily
blocked.
1.4.4 Flat
A flat membrane is supported by a porous plate through which the permeate
leaves. The feed is passed at high speed across the surface of the membrane between
the spacers or flow channels, which are 0.2 to 4 mm high. Permeate passes to the
interspace between the coupled pairs of membranes and is led out through a header.
Chapter I 17
.. I I ..
-..: ----"1'"'--...;,. CQNCEHTRATEOUT
PERMEATE OUT
FEED SIDE
SPACER
POROUS
SHEET
OI/T
RECIRCUlATlNG
FLOW INLET
SuspenSion
Table 3
Comparison of Configurations
Type Tube Hollow Spiral Plate Leaf
Fibres Wound Frame
Flow type T La La/f T T
Simplicity of flow path G F F P F
Resistance to mechanical damage G G P G P
Lack of suspects to blockage G P P P P
Hold-up volume P G G G G
Ease to mechanical cleaning G F P F P
Ease of isolation of small volume G P P G P
Power costs of unit penneate rate P G G G F
Prefiltration N Y Y Y Y
Field replacement G G G F F
Typical module life (years) 2-6 1 1-2 1-2
Membrane surface vs. volume Lo H H M M
Investment cost H M Lo H H
1.4.5 Pleated
Membranes can be casting or gluing on to the surface ofirregular shaped tubes
for form filters. There are also inside and outside forms for filtration (Fig 4£).
The advantages and disadvantages of this form are the same as hollow fibres,
but the uneven flow pattern may result in sanitary problems.
There are also dead-end configurations: stirred and unstirred batch cells (Fig
5), which are mainly used for laboratory or for shear force sensitive materials. Since
they are not related to crossflow, they will not be discussed here.
Membrane
Permeate
am, Cm V1
ME..mcJdi1le
Concentrate
Qp,Cp
Feed Recirculating
pump pump
Fig 6 Basic operating diagram
It is ideal for the control of microbial growth owing to its short residence time,
the mechanical stress on the liquid and required energy is also smaller than other systems.
But its flexibility is low, and it is very difficult to get a high final concentration.
Chapter 1 21
Permeate
Feed Concentrate
Om, Cm
Concentrate
Feed Recirculating
pump pump Permeate
Fig 8 Batch system
F,e
Feed Recirculating
pump pump Permeate Qp, ep
Fig 9 Continuous system
1.5.3 Continuous
A small pump feeds dilute liquid into a circuit in which a large pump
recirculates it continuously through the membranes. The concentration takes place
totally within the recycling loop and none of the concentrate is returned to the tank, (i.e.
the feed back flow Fb = 0). The concentrates within the loop will, therefore, increase
to the desired degree. Then the concentrate is bled from the system. The rate of the
feed must be equal to the sum of the bled and permeate so that the concentration within
the circulating loop is the same as that of the concentrate product.
In a single continuous system, the residence time of the product is short (only
a few minutes), significantly reduces the possibility of product deterioration, however,
Chapter 1 23
since the system is running at high concentration, the permeate flux is low, the required
membrane area will be higher and the yields of retained species lower than that for a
batch system of the same overall capacity.
A multistage system (Fig 9) will overcome this shortcoming since only the
final stage will be operated at the highest concentration, the total permeate will increase,
the residence time shorter, but it is more expensive because of the necessity of process
control.
1.6 Applications
This method was widely used in Germany after World War II meanwhile the
Americans used it for culturing coliform and Sallmonella for military uses.
In the 1970s, the "track-etch" membranes were used for trace element analysis,
microscopic analysis [Davis et ai, 1974], blood rheology studies [Chien et ai, 1971]
and crossflow plasmapheresis [Castino et ai, 1978; Zydney & Colton, 1984].
clarify musts [Drioli & Molinari, 1990] and wines [Peters & Pedersen, 1990], harvest
yeasts from cider [Taddei et al, 1990], prepare fruit juices (apple, citrus, etc) for
fermentation, sweetening, sterilizing and concentration [Kilham, 1987].
Besides the above, MF is also used for the purification of sugar solution
[Punidadas & Decloux, 1990] and vinegar [Ebner, 1981].
It has been used for processing fermentation broth by filtration and diafiltration
for cell recovery, product removal, filtration in conjunction with continuous fermen-
tation and substrata purification, such as:
- remove pyrogens or bacterial endotoxins from the liquids for pharmaceutical
use [Blosse, 1982];
- recover enzymes from process [KrOner et al, 1984];
Chapter 1 27
The membrane resistance always exists during the filtration, other resistances
mayor may not exist depending on the properties of the processed materials and
membrane as well as the operating conditions.
Crossflow 0 0
•
(Rc)
RAO
t tt
Permeates
These mechanisms are the resultant of multiple forces such as shear, diffusion,
electrostatic attraction and repulsion etc., depending on the characteristics of the fluid,
particles, membrane and the operating conditions.
Chapter 1 29
a) By fluid-panicles-membrane interaction
The fouling may be caused by the interaction between the solutes or panicles
and the membrane due to the differences in the distribution of electrons in their atoms
or molecules [Jonsson & Kristensen, 1980]. This will result in the fonnation of a
number of different types of bonds like ion-ion, ion-dipole and dipole-dipole bonds:
Jackson & Landolt (1973) found that a nucleation-growth mechanism
controlled the membrane fouling;
Bhattacharyya & Grieves (1979) found that the detergent-water system caused
reversible detergent-membrane interaction which led to flux rate decay;
Hopfenberg et al (1973) found that ion characteristics, surface activity of solute
molecule and surface charge of the membranes are vital to the occurrence and magnitude
of fouling;
Palmeretal (1973) concluded from their UF experiments that solute-membrane
interaction occurred at low solute concentration;
Kesting (1971) found that hydrolysis existed for cellulose acetate membrane
which also caused flux rate decay.
b) By mechanical effect
Due to the structure of the membrane and the shape of the panicles, the particles
may clog the pore externally and internally by impingement.
High pressure will also increase the fouling if the membrane or foulant is
compressible.
c) By membrane properties
The membrane properties such as pore size distribution, pore shape, length
and tortuosity, zeta potential [Freeman, 1976] and surface tension, surface charge,
surface potential [Lee, 1977] may influence the fouling process.
e) By pH value or temperature
pH value will change the charge of the foulant and result in the change of ionic
strength and solubility. It also influences the panicle sizes [Winfield, 1973; Lee,
Chapter 1 30
1977].
High temperature may change the nature of the foulant and therefore influence
the fouling [Hayes et ai, 1974; M.uller et aI, 1973].
(1.1)
b) Removal forces
Apparently, the surface tension force is not a major force in crossflow
membrane system, therefore, the principle of improving the flux rate decay is how to
remove the attached particles from the membrane by overcoming the van der Waals
force and the electrostatic attractive force. The removal forces can be divided into two
main groups: vertical forces and axial forces. The vertical forces include increasing
the backward movement of the particle by diffusion, electrostatic or magnetic repulsion
and mechanical vibration; the axial forces aim at dragging the particles away from the
surface by increasing the shear force of the fluid or sweeping with scouring materials.
Besides, pretreatment of the particle, fluid or membrane to reduce the adhesive force
is also effective.
According to the above analysis, the decay can be reduced but not eliminated
by changing the operating conditions such as increasing the cross flow velocity or
decreasing the transmembrane pressure. However, the flow velocity can not be too
high (usually less than 5 rn/s) and in some cases, there is a threshold of velocity above
which the flux rate is unaffected, and the transmembrane pressure can not be too low
otherwise the flux rate will be too poor, and therefore, not practicaL
These techniques are used before, during or after the filtration depending on
the nature of the foulants, membranes, products and the used equipments. Some of
these techniques are listed here:
I) Electric fields [Bowen & Sabani, 1992; Wake man & Tarleton, 1987];
2) Acoustic and electro - acoustic fields [Wakeman & Tarleton, 1991];
3) Backflushing [Holdich et al, 1990; Jaffrin et al, 1990];
4) Turbulence promotors [Oejmek et al, 1974; Shen & Probstein, 1979;
Light & Tran, 1981; Poyen et al, 1987];
Chapter 1 32
CHAPTER 2
(2.1b)
(2.lc)
where a is a constant
ac,
J. ax is convective transport towards membrane
On the assumption that the filtration is under steady state and D is a constant,
Eq 2.2a can be solved to obtain:
D Cl-Cp
J.=-ln C (2.2b)
x Cb - p
where Cp is the concentration of the filtrate (kg om· 3)
Cb is the concentration of the bulk flow (kg om·3 )
D/x is the mass transfer coefficient represented by k later (mos")
Chapter 2 35
membrane membrane
.. p
.. p
Cp Cp
-x o x
a) Cake-filtration type b) Film-filtration type
t~-lnUJ (2.3a)
(2.3b)
Chapter 2 36
where k is mass transfer coefficient (m.s· l ) and equals to Dlx where x is the
diffusional distance.
If C p = 0, then:
C,
I =kln- (2.7)
v Cb
a) In laminar flow
The Graetz (1885) or Leveque (1928) solutions for convective heat transfer in
laminar flow channels, suitably adapted for mass transfer, can be used to calculate k
for retained materials diffusing away from the membrane surface. Funhermore, when
diffusivity is very low, the CP boundary layer is much smaller than the channel height
when axial distance is small compared with the entrance length. Under such conditions
(usually applicable to macromolecular solutions whose diffusivities are of the order of
10> m'tsec) the rigorous solution for the prediction of k can be approximated by Leveque
solution [Leveque, 1928]:
(2.8)
4U
Circular tube y= dl2 (2.9b)
Chapter 2 38
Triangular channel
30U((5;)+12)((27-b)2 +20 ) (2.9c)
a a
Shen & Probstein (1977) considered that the difference between theory and
experiments could be due to variable transport properties of the macromolecular solution
normal to the membrane surface in the concentration boundary layer. The results of
their theoretical analysis were that the concentration dependence of viscosity has little
effect on the limiting flux but the diffusivity dependence of the concentration could not
be ignored. Probstein et al (1978) found out, by means of an integral method, that
the appropriate diffusivity defining the flux in the gel-polarized region was that at the
gelling concentration, rather than at the bulk concentration. This means that the
diffusivity coefficient calculated at the bulk concentration in Eq 2.10 should be replaced
by one evaluated at the gel concentration to give:
UD 2)O.33 C
J v = 1.31 --g In--.! (2.11)
( d.L Cb
Chapter 2 39
The formula apparently agreed well with the experimental data they quoted
when the gel concentration was large compared to the bulk concentration in macro-
molecular solutions.
Trettin & Doshi (1980) claimed that the disagreement between theory and
experiments was due to the inaccuracy in the film theory. They used, instead, an
integral method to solve the mass balance equation:
dC
V dC +U =!!...(DdC) (2.l2a)
dx dy dx dx
where V is the radial flow velocity (mos")
y is the axial distance (m)
x is the radial distance (m)
By assuming linear velocity and a second order polynormal concentration
profile, they obtained a closed solution expressed in dimensionless variables:
~
J; =T
F -I "
[KF.l' (D .)' (2.12b)
•
where J v+ = dimensionless permeate velocity
=Jv(hm)
. (3X )0.33 (D b")-<l.33
. D.
D=-
• Db
a = 3V/dh
Fg = CP modulus Cg/C.
= 2b 2/(b+l)(b+2) b=flFg)
K
When b=2 K = 2/3, Eq 2.12b equals EqI2.1]' When CglC. <4, the theoretical
solution agrees well with the experimental data, while CglC. >4, the real flux is lower
than that predicted by the model [Trettin & Doshi, 1980].
Chapter 2 40
b) In turbulent flow
There are numerous correlations involving the Sherwood (Sh), Schmidt (Se),
Stanton (St) and Reynolds numbers (Re) such as:
(2.14)
(2.15)
Chapter 2 41
a) Filtration models
This submodel assumes that solids which are larger than the membrane pore
size will be retained. The flux in the pore is mainly viscous and can be expressed by
Poiseuille's law:
Nm • 1t • d~ • Pt Em· d~ • P,
(2.17)
J, 12811. Om 3211. Om
The total resis lance Rc in the boundary layer can be expressed by deposit layer
thickness XI and specific resistance r l (m· 2)in the form:
Chapter 2 42
(,
R, =)0 r , • dx (film type) (2.18a)
(2.19)
(2.21)
Sa
SD =[2( 1- d",
d,)2 - ( 1- d",
d, )4] • [1-2.104(d,d", ) +2.09( d",d, )3 +0.95(d",d, )5] (2.22)
! = 1( 1 +~ aiC i) (2.24)
s ~ .=1
R=
t
~
JlI
• V • Sib
3 a·
C-C+L-'
j = 1i + 1
.
I
. ] (1--
(C'+I-C<+I)
b
VI)
Vo
(2.26)
(2.27)
Chapter 2 44
For non-slip conditions and turbulent flow, the most popular correlations used
are based either on the Chilton-Colbum (1934) or on the Deissler (1959) analogies.
Sh =0.023Reo.sSeO.33 Se < I (2.30a)
which k is correlated with the friction factor f In this treatment it is usual to substitute
Sh for Nu and Sc for Pr [Bird et ai, 1960].
. k
Jo=- c =-
S; f (2.31)
U 2
2) Based on eddy diffusivity models
This model assumes that eddy diffusivity D.ddy =D.ddy{x+} varies with the
distance from the wall and how the duct is sectioned [Harriott, 1962].
In some of these sections molecular or turbulent or both types of transfer are
considered effective. The resultant Sh correlation by this model can be described by the
asymptotic form (at high Sc number)
12
Sh-!' SC • (2.32)
where a is 0.25 to 0.33.
This model suffers from the drawback that D"'dY can not be experimentally
observed or measured.
Table 4
Levich's "Three-Zone" model
However, under high Sc number conditions, the turbulent mass transfer to a solid
boundary is very little controlled by those velocity fluctuations which contain most of
the turbulent energy.
6) Based on experimental data
b) For viscoelastic fluids
In this type of fluid, the friction factor / has to be measured, since the lower
the /, the lower the mass transfer coefficient k (k-r). Some results according to the
work of Gekas & Hallstrom (1987) are also listed in Appendix 2.
In fact, the empirical correlations agree with most of the theoretical models
with a Re exponent in the region of 0.71 - 0.73 and a Sc exponent of 0.33. The lower
value of Re in comparison with values of 0.75 - 0.90 for Newtonian fluids can be
explained by friction factor decrease.
c) For power-law fluids
Due to CP, itis possible for some solutions to show non-Newtonian behaviour.
In the power-law cases, the flow index n must be known. Some results on this can be
found in Appendix 2 according to the work of Gekas & Hallstrom (1987).
~. R,
b=--
S' P,
S is membrane surface area (m').
Chapter 2 48
Nakao et al (1990) found that initial penneate flux decay within 5 to 10 minutes
can be well predicted by above equation.
Rushton & Aziz (1984) concluded from their filtration experiment of dilute
suspensions of various mineral slurries that this equation might be used to describe the
process of particulate polarisation.
b) By specific resistance
P,
Since 1=-- (2.1a)
• Jl • R,
Sabuni (1990) assumed that only certain particles will be retained at the
membrane surface to fonn the cake as those in the traditional cake filtration, other
particles will be re-entrained into the bulk suspension. He modified R, as:
R
e
re • Qo • C (
S l-e
(-f))
0
(2.35)
Mikhlin et al (1982) assumed that both turbulent eddies and shear force had
an effect on moving deposits. They presented:
re • Jl • C • 120 • t
(2.36)
P,
Chapter 2 49
v [ (c.)
J = k ° In -
Cb
Pbdx]
+--
Cb dt
0_
1
Cb
(2.38a)
Hiddink et al (1980) predicted the flux rate in the RO of whey and skimmilk
accounting on the resistances caused by fouling, Rc and R,.:
(2.38b)
where sub 1 and 2 refer to the resistance caused by fouling and CP.
Belfort & Mark (1979) converted the cake filtration model into a modified gel
filtration model by adding a third item (a/W) on the right side of the equation and then
normalized different membranes with fouling and compaction.
For the initial transient period:
t a3
-=aW+n~+ (2.39a)
W I -z W
Chapter 2 50
(2.39c)
Gutman (1977) predicted the flux rate based on turbulent burst theory, his
model will be discussed in § 2.4.
(2.42)
Sharma & Yortsos (1987) predicted the pore size variation with time:
Grace (1956) made a thorough study of the Standard blocking model and
deri ved the formula for calculating the pore length and density based on a mass balance
equation and Poiseuille's law on the assumptions that:
1) parallel pores of equal length and radius,
2) during a certain period, the initial pore diameter must be at least several
times greater than the particle diameter whatever the solid concentration, and
3) the capture is a direct interception of particles from the streamlines adjacent
to the pore walls, and the volume of major flow channel through the pores decreases in
direct proportion to the volume of filtrate passing the pores.
Chapter 2 52
4Cpo" 1
(2.440)
1tS d;, (1-e,) - p,A
-0.. =B -,,:::::--...:.
1td!S P,
(2.44b)
N.. 1281l
~ (0.. - N.. ) - ( !: )=
Cpo,• • d;' • Pt· B
0.. = (2.44c)
321l - (1 - e,) - p, - A
.
N=
(0.. - N.. )
(0.. IN.,)
1
1t - S - d~
512C,a" -Il
P, (l-e.)-AB
(2.44d)
where Cpore is the particle concentration of the fluid inside the pores (kg_m·3 )
A and B are the gradient and intercept in Eq 2.4f:
rIW=A-t+B (2.44e)
When om. Nm•A and B have been obtained. the initial pore size of the current
run can be estimated with the intercept B by Eq 2.44b:
-Il)'
I
1280.,
d =( (2.44.1)
m 1tN.,S P,B
or alternatively with the gradient A by Eq 2.44a if Cpore and e, are available too:
Chapter 2 53
(2.44g)
Shirato et al (1979) and later Hermia (1982) applied the four blocking models
to the constant flux rate or constant pressure filtration with power-law non-Newtonian
flow.
A general correction for the effect of flux on the mass transfer coefficient is
the Stewart correction [Bird et ai, 1960]. Recently Gekas & Hallstrom (1987) suggested
the introduction of an Se correction factor (Sc/Scw )O.1I in an analogy with heat transfer
correlations.
Baker et al (1985) correlated flux rate with feed flow rate by:
J. =7.4 • 10-5 UO. 6 (2.45a)
Jv oc = 1 - 3 m·s· l .
U1.2 U
J v oc pl.O P = 10000 - 30000 kg.m·2
J oc CO C = 0.51 - 30 kg·m·3 •
v
Van et al (1979) presented six models with four parameters (J,C,U ,9) to
describe the flux rate of cows' milk within the pressure plateau area. The following one
was thought to be the most reliable:
-0.67239
Peri & Setti presented a four parameter model (J,U,C,P) on the flux of
skimmed-milk (1976a) and sweet whey (1976b) under constant temperature.
for sweet whey:
for skimmed-milk:
Cheryan & Nichlos (1980) presented a four parameter (J,U,T,P) model of the
flux in processing water extracts of soy beans:
Iv = 0.782 + 0.026(T - 273) +0.OO9U + 0.105P (2.45f)
Iv = AU·C; (2.45g)
Chapter 2 55
Matthews et al (1978) used cake theory to present a two parameter (1, W) model
of sulphuric acid casein whey:
J.=JoW'" (2A5h)
~( U )0.
J. =a l llz e 500 (2045i)
Hunt et al used the term of eddy diffusivity and developed two four parameter
models (V, P, Cb' d) for steady-state (1987a) and unsteady-state (1987b) microfiltration
with short tubular modules:
For steady-state:
(C,) 2
J. =d• • D.ddy • In Cb [rh - (r. - xJ ]
2 -I
(2045j)
For unsteady-state:
Cb - C, • exp[-a(r; - (r. - x - xi)]
J, 2 2 (J, +J) (2045k)
1- exp[-a(r. - (r. - x - XI) )]
where
(2.451)
Table 5
Parameters in Mahenc's (1986) model
Most of the models (suction or injection) have been for slits, tubes and annuli
since they are the common geometries for membrane systems. Two categories of
problems have been solved: fully developed flow where the shape of the non-dimensional
velocity profiles is considered similar or constant with axial distance, and the developing
flow at the duct entrance where the shape of the non-dimensional velocity profile is
changing with axial distance. Most of the work except Galowin et al (1971, 1974) and
Terrill (1983) assumed that k is constant along the duct. Numerical solutions assuming
constant wall suction and similarity of velocity profiles are summarized by Berman
(1958) and White (1974).
Most of the studies have been conducted for turbulent flow of air [Weissberg
& Berman, 1955; Weissberg, 1956; Wallis, 1965; Aggarwal et ai, 1972; Brosh &
Winogard, 1974] and for laminar flow of air [Bundy & Weissberg, 1970] in porous
tubes.
Chapter 2 57
Singh & Laurence (1979a & 1979b) used numerical methods to solve the flux
under slip velocity conditions for slit and tubular systems. They solved the equation of
motion in 2-dirnensions by a first-order perturbance method and diff!lsion equation by
a finite difference technique. They concluded that CP decreased with an increased slip
coefficient since slip velocity enhanced back-diffusion of solutes. The flux rate, on the
other side, will increase.
Some work in this field during 1934 to 1986 has been surveyed by Belfort
(1986) and interested readers are referred to this work for further details.
For particles and macromolecules it has been found that the back transport of
solutes was well beyond the ability of diffusional force or shear stress. In order to explain
this phenomenon, other forces are considered. These forces can be either parallel or
vertical to the membrane surface.
a) Vertical forces
There are four sources which are considered able to make the particles move
perpendicular to the local direction of flow [Cox & Mason, 1971].
I) Body forces e.g. gravity and buoyancy force if the membrane is horizontally
placed, or centrifugal force.
It is no doubt that for the range of microfiltration, both gravity and the buoyancy
forces are too weak to remove the deposit from the membrane surface.
Centrifugal force is strong enough as long as the rotating speed is high, it has
been one of the conventional technologies of separating solids from gas or liquid in
the cyclone and hydrocyclone. However, this force only exists in rotating flow which
is induced, and therefore is considered later in another chapter.
Chapter 2 58
(2.47)
It is believed that some of these forces might play an important role in the
difference between predicted and experimental data. The "Tubular Pinch Effect" is
thought to be one of such effect caused by inertial force near the membrane.
Segre & Silberberg (1962) first published their observations of the tubular
pinch effect on dilute suspensions of rigid spheres in a solid wall tube where the particles
migrated away both from the tube wall and tube axis, reaching equilibrium at an eccentric
radial position. This phenomenon was reported by Karnis et al (1966) from their
experiments on many kinds of particles in various conditions and flowing media.
The extensive surveys of both experiments and theories of this effect have been
made by Brenner (1966), Goldsmith & Mason (1967), Cox & Mason (1971), and later
by Leal (1980).
VL ="9
I URe (d )4(X )
s
rh rh
(2.49)
Chapter 2 60
In order to explain the two-way migration of the particles, Cox & Brenner
(1968) obtained a first-order solution of the Navier-Stokes equation and computed the
lateral force required to maintain the sphere at a fixed x:
(2.50b)
where / (x/(rh) } is a function of the radial position of the particle in the tube
or slit.
This equation is close to the empirical equation used by Segre & Silberberg
(1962) to correlate their data:
(2.5Oc)
rh rh XII!'
V
L
=id;
V
-/-
rh
{x} (2.5Od)
The position dependence/( x/rh} is a maximum at the wall with a value ofO.095
[Vasseur & Cox, 1974] or between 0.26 and 0.42 [Ho & Leal, 1974].
All the works above have dealt with particle motion in a non-porous duct. It
was Porter (1972) and Henry (1972) who applied the theory of "Tubular Pinch Effect"
to explain the higher flux in experiments than predicted.
Madsen (1977) suggested that the lift velocity and filtration velocity estimated
from polarization theory are additive, with the filtrate flux given:
J =V +kI
JC ) (2.50e)
• L '\ Cb
Chapter 2 61
Green & Belfort (1980) proposed a model which explicitly considers the
build-up of an immobile particle cake at the membrane that limits the flux according to
Pr
J=- (2.1a)
v ~Rc
where (Sjv,) is the particle specific surface to volume ratio (m· l ), this
expression is, in fact, the Kozeny-Carman equation.
_ (ds)b f{x}
VL=aURe r. (2.50f)
where a = 5
b = djrh
Xe = -0.7 for best empirical fit.
Zawicki et al (1981) employed Saffman's (1956) analysis in their model,led
to a formulation known as deposition theory [Forstrom et ai, 1975] in which the drag
force due to filtration is balanced by hydrodynamic lift force. Particle diffusion is entirely
Chapter 2 62
neglected. They assumed that there is a particle free layer immediately adjacent to the
membrane when the lift force exceeds the drag force. The maximum flux is thus given
by:
,
d,Y
J. = VL = 0.34-, (2.50h)
A.j.!'
where A. is a correction factor for the drag force on a spherical particle in a
concentrated suspension [Trettin & Doshi, 1980]. The deposition theory did not agree
well with the experimental data [Werynski et ai, 1981; Zydney & Colton, 1984].
(2.50i)
Altena & Belfort (1984) studied spherical rigid neutrally buoyant particles
moving in a laminar fluid flow in a slit with one porous wall, where the wall flux was
constant and independent of the axial coordinate. By extending the analysis of Cox &
Brenner (1968), the effect of the wall porosity had been taken into account, they
obtained the lift velocity in dimensional form.
(2.53)
However neither this model, nor that of Madsen (1977), and Green & Belfort
(1980) incorporated any correction in the lift velocity expression for the presence of
other particles in a concentrated suspension.
Most of the existing models on the "Tubular Pinch Effect" were derived for
laminar flow although Porter (1972) proposed that this effect should be greater in
turbulent flow because of the larger inertial. effects caused by. radial migration velocity
will increase with the Reynolds number, fluid velocity, and particle size but will decrease
with increasing channel dimensions. Most CFMF applications use turbulent flow and
have small particles suspended, hence radial migration should not be a dominant force.
4) Turbulent burst
Turbulent burst is a natural physical phenomenon which occurs in the turbulent
sublayer boundary. It is the result of the evolution of small streaks along the wall (x+
< 100, where x+is the normalized vertical distance from the wall). Since itis responsible
for most of turbulent energy production from the boundary layer towards central flow,
particles suspended in the boundary layer will certainly be affected by it. Most of the
studies on turbulent burst have been concentrated on experimental observations and the
determination of the average time between two bursts [Antonia, 1981]. The development
of the theoretical nature is relatively slow due to the complexity of the mathematical
expressions. The details on turbulent burst has been surveyed by Bogard (1982).
Grass (1971) observed that sand particles were carried up from ·sea bed region
through virtually the total turbulent boundary layer thickness.
Sumer & Deigaard (1981) traced the motion of a single 3.0 mm diameter
particle suspended in a horizontal water channel. They found the particle motion to be
in accordance with available information on the burst phenomenon and deduced that
turbulent burst might be the mechanism which maintains particles in suspension.
Roger & Eaton (1989) observed that the particles did not closely follow the
fluid fluctuations in the normal direction and also the presence of particles tended to
suppress turbulence.
Chapter 2 64
Cleaver & Yates (1973) were the earliest authors who attributed particle
re-entrainment to the turbulent burst:
2
FL =0.076 Pb v [ -v-
d,U
*J3
(2.51)
FD =8Pb V
2
(d-v-*)2
,U
(2.52)
where FD is the drag force for steady flow parallel to the wall past a sphere
and in this case FL = O.
From Eq 2.51 and Eq 2.52, if the particles are small, d,u*/v ~ I, then FL «
FD, which is coincident with observations [Clark & Markland, 1971]. The lift force will
only remove those particles whose sizes are larger than (0.005/'tw r-o·75 (where 'tw is the
wall shear stress).
The rate of lifting will be
therefore
. 100v
nB =N B - - (2.54c)
u* 2
(2.54d)
Gutman (1977) related the theory of turbulent burst to the fouling mechanism
of crossflow membrane filtration. Based on the postulation of Cleaver & Yates, he
proposed a mathematical model for particle removal from RO membrane surfaces:
.!.. = 1 + _~
JF
CF[ 1 _ exp [_...:.-f-_1----:-J-::-Au_t
Au l+~cF
Au
II (2.55a)
(2,55b)
~= RF (2.55c)
Rm
where RF is the hydraulic resistance of fouling layer per unit mass;
A is the parameter (s om- 2)
PbSB
A =-,'-:-:,-- (2.55d)
100uB
where SB is the fraction of surface cleared by turbulence burst (m2);
uB is the superficial liquid velocity (mos-').
Knibbs (1984) applied this model to the UF of a ferric hydroxide floc and found
the rate of mass re-entrainment was the product of a bursting rate coefficient and
deposited mass. The bursting re-entrainment was an increasing function of crossflow
velocity.
However, Yung et al (1989) modified Cleaver & Yates' models (1973 &
1976) by pointing out that the rate of re-entrainment is not directly proportional to the
frequency of the bursting actions and the residence time of the deposited particles will
be much higher as suggested in Cleaver & Yates' (1976) theory. They concluded that
for particle sizes smaller than the viscous sublayer thickness, the tangential drag force
is the dominant re-entrainment force, the removal criterion for small particles where
adhesive forces dominant becomes:
(2.56a)
,,
Fig 13 The interaction between turbulent burst and particles
They concluded that for panicles with tI; > I, the transport is controlled mainly
by ejections originating from the lifting up and breakdown of the low-speed streaks in
the wall regions. When the particles are introduced into the flow, they mostly accumulate
in the low - speed streak of the wall structures. These particles are then lifted up
(depending on their size and density) by the inclined vortex -loops of the wall regions
and are ejected into the bulk flow. The ejected panicles with a greater density than
that of the fluid, will eventually come back to the wall region, where some of them
encounter the wall ejections which have already been in progress and will be lifted up
before reaching the wall regions. The bursting process repeats itself and dominates the
panicle transport, . while the particle presence affects the mechanism by which the
turbulence energy is transported from the wall region to bulk flow.
The reported bursting process causes the transport of the particles in the flow
direction. tl z • = SO, and inclined angles of the vortices are about 20 - SO • to the
boundary at x· < 20. (Fig 13)
Chapter 2 68
They also found that the panicle-burst interaction is very dependent on the
density, size and flow Re of the particles. The angle and maximum elevation lifting
up decrease:' with increasing panicle size and density. Meanwhile the lifting process
increases with increasing Re.
The panicles with size d: < I have no response to burst, which meets Yung et
al's (1989) conclusions.
Therefore, although some authors have made positive conclusions, the sig-
nificance of turbulent burst on the membrane fouling mechanism is still not yet clear
since the phenomenon of permeation is similar to wall suction which will suppress the
turbulent burst by reducing the probability of the breakdown of low-speed streaks and
therefore increasing the period between two ejections; the existence of panicles will
also reduce turbulent bursts. Besides, the panicle size will be important to the interaction
with turbulent burst, the small particles will not be influenced by the occurrence of
turbulent burst - they only "roll" along the wall surface.
b) Axial force
There are three types of models which owe the removal of panicles to the axial
forces.
1) Axial convection force
(2.57)
resistance which is a function of H, and after some approximations, they found that by
assuming H;;:: 251lm, the predicted values of this model met with selected plasmapheresis
results but still gave some discrepancy.
Davis & Birdsell (1987) developed this model by using the parabolic velocity
profile and predicted that a flowing cake thickness is a function of axial position x.
Hoogland et al (1990) assumed that the removal of solids towards the
membrane is accomplished by converting these solids into axial directions and finally
out of the filter module. They used Kozeny-Carman equation and obtained:
(2.58)
However, it has been confirmed that a packed static cake has more influence
on the permeation and therefore this model has limited significance.
2) Scouring force
This model is based on an analogy between the flow across the cake and the
motion of a sediment-laden stream over a layer of settled sediment. Under steady state,
the convection velocity of the particle towards the membrane is equal to the rate of
scouring a particle from the membrane surface, which is proportional to the shear rate.
Fane et al (1982) used the idea of an "erosion coefficient" which is a function
of bulk concentration and set up the relationship between permeate flux rate , bulk
concentration and velocity:
(2.59)
They further developed their model (1984) by intuitively combining the three
forces (Brownian diffusion, lift and scour) together:
(2.60)
This model was comprehensive and met well with their experimental results.
Chapter 2 70
3) Force balance
This model is based on the balance between the resultant axial force, which
tends to remove the particles, and normal force which tends to retain the particle. The
axial force is thought to be constant since the bulk velocity is constant, and the normal
force will decrease due to the decay of the permeate flow rate. In the initial stage, the
normal force is stronger than the axial one and hence causes the deposition. The steady
state occurs when the two forces are balanced and results in constant cake thickness and
permeate flux rate.
Shirato et al (1970) analysed the forces acting upon a particle which sits at the
surface of the particu1ate bed, they proposed that during penneation, there exists a
critical axial velocity at the bed surface, over which the particle can no longer keep
static and removal is possible.
Rautenbach & Schock (1988) showed from their tests with the cross flow
filtration of 2 - 2.5 micron clay and quartz powders in tubular and thin-channel modules
that:
0.44
126 Vds
J,=aRe' ( d. )( d. ) (2.61)
also complicated the estimation of a friction coefficient and boundary layer velocity
profile. The continuum theory forwarded by Willis et al (1986) and statistical mechanics
theory by Mason & Longsdale (1990) might be helpful to solve this problem.
Navier-Stokes equation is the basic equation for CFMF. The various solutions
to it provide different expressions for the filtrate flux depending on the assumptions
made.
Concentration polarisation is studied by most authors working on membrane
separation experimentally and theoretically. There is substantial discrepancy between
experimental data and theoretical prediction in most cases.
None of existent models, neither the famous "Tubular Pinch Effect", nor the
popular "SelfInduced Hydrodynamic Diffusion" or other mechanisms have successfully
explained the origin of the discrepancy between equilibrium flux rates based upon
particle diffusion coefficients calculated by means of a modified Stokes-Einstein
equation and experimental measurement.
Pore blocking, on the other hand, is also an important factor for flux decline,
especially because it affects membrane resistance. The blockage can not be simply
improved by cross flow since the pore flow is essentially laminar and the adhesive force
in the micron or submicron range is very strong. A major task for all workers interested
Chapter 2 72
CHAPTER 3
Many possible applications have been described in § 1.6 for the uses of
inicrofiltration, such as ultra-pure water production, fermentation product processing,
precipitate concentration, etc ..
The process scale requirement is appreciably large for the duty of seawater
filtration, yet the specification of the particle retention is not very demanding, when
compared with biological or ultra-pure water applications. Under these circumstances
seawater filtration was thought to provide a good challenge to both the existing math-
ematical models of the process and the robustness of the crossflow filtration technology.
Another case of cross flow filtration of seawater is in the fish industry in which
a combination of UF and MF for waste water treatment is used as described in Chapter
1 [Jaouen et al, 1990; Schmidt & Wulle, 1988; Watanabe et al, 1986}.
The offshore oil industry also requires large amounts of filtered seawater to
inject into the oil reservoir rocks to maintain the pressure and displace the oil. 98 %
of the particles larger than 2 Ilm in the injected water must be removed before injection,
so as to prevent deposition and blockage within the oil reservoir rocks [Mitchell &
Finch, 1981}. This specification assumes a constant feed suspension and an alternative
specification is less than 2000 particles per ml greater than 21lm and absolute filtration
at 51lm [Holdich et al, 1990]. The required volume of water flood will be as high as
2600 m3/hr for a field and rarely less than 650 m 3/hr [Abdel-Ghani et ai, 1988}. Some
production platforms now employ RO on the injection water to reduce the concentration
of sulphate ions present, thus reducing the precipitation of barium sulphate in the rock
formation. Crossflow microfiltration could be employed to pretreat the water before
RO.
Filtration is also used to protect equipment which uses seawater on the oil
platform: RO, water sealed pumps, cooling, etc. On some platforms over 50% of the
water drawn up from the sea is used for duties other than injection.
These tasks are currently being carried out mainly by backwashable deep bed
or disposable cartridge filters [Kaiser, 1983; Cubine & Randolf, 1973}. These facilities
work adequately over a large part of the year, but do not perform well during periods
of algae bloom since they are run in the dead-end mode and usually suffer from clogging
and low flux rates due to the retained particles. Water used for cooling duties is at
present filtered on 80 Ilm coarse screens.
The North Sea seawater used in reservoir injection is reasonably clean, containing
between 0.2 and 0.8 mg/1 of suspended solids [Mitchell, 1978; Carlberg, 1979], a
consequence of having been pumped up from a depth of 60 m [Mitchell, 1978].
The major contaminates are clays, sand, bacteria and plankton which are usually
filtered out in deep bed or cartridge filters. The seawater solids loading is highly seasonal:
the quantity of suspended solids increases considerably during spring and autumn due
to the "bloom" of plankton. It has been reported that the major foulant found in seawater
cartridge filters is the lipid content of plankton [Edyvean & Lynch, 1989], which is
Chapter 3 75
released into suspension when the organisms are crushed by the pumps and filters. The
resulting lipid concentration can rise to as high as 20 mg/! during a bloom period
[Edyvean & Sneddon, 1985; Volkmann et al, 1980]. The lipids are fatty materials
which act as a glue to stick the suspended solids to the filter surface and cause blockage
[Edyvean & Lynch, 1989].
Since the 1980s, with developments in the technology of manufacturing and
applying membranes, there has been an increasing interest in utilizing crossflow
membrane microfilters to replace conventional filters.
During crossflow filtration, the operating pressure will be lower than that during
conventional filtration, the feed flow is parallel to the membrane surface, therefore the
shear force will greatly reduce the deposition at the membrane surface and result in
higher flux rates, longer membrane lifespan, lower costs and easier maintenance.
One purpose of this study was to investigate the feasibility of using crossflow
microfilters for offshore applications and to obtain information on potential fouling
problems.
filtration of simulated seawater. It used PVC pipes of 3/4 inch. It can accommodate
either tubular or capillary membrane modules.
The principles of the layout of the two rigs are the same as shown in Fig 14.
D1
P1
Crossflow Filter
HiaclRoyco Sizing
V1 B3 Equipment F1 F3
F2 B2 D2
Thermometer B1
To Tank
Centrifugal
0.1 urn Pump
Cartridge Filter
Drain
In Fig 14:
B 1 to B3 are ball valves. B 1 controls the by-pass flow, B2 only opens for system
cleaning together with opened V2, B3 is used to control the permeate side pressure.
Dl and D2 are diaphragm valves. Dl controls the outlet pressure while D2
regulates the inlet flow rate.
PI to P3 are pressure gauges. PI and P2 are used to measure the pressure at the
inlet and outlet of the module, P3 is used to measure the pressure at the permeate side,
the pressure range is 0 - 6 Bar.
.
The inlet flow meter Fl is a rotameter, its measuring range is 0 - 221/min. The
other two flow meters are both Litre Meter electrical type with different ranges: 1 - 65
Chapter 3 77
Vmin for the F3 which is on the concentrate side and 1 - 12 Vrnin for F2 which is on the
permeate side. They are alternatively connected to a CR450 chart recorder depending
on the requirements of the tests.
TI is a three way valve which alternates the permeate and feed flow through the
HiaclRoyco sizing equipment.
In the case of air backflushing, only one centrifugal pump is used for feeding
the flow throughout the system. The air is supplied by the pipeline and its pressure is
set at 3.5 Bar. The air is filtered with a 0.1 ~m cartridge air filter before it enters the
module, this filter is not included in the figure.
If water backflushing is involved, another pump and another tank are needed.
The required water comes either from the permeate or from the 0.1 ~m cartridge filter.
It backflushes at 2.8 Bar. The layout of the backflushing part has not been shown in the
figure except for the pump and the solenoid valve.
A HiaclRoyco laser light particle sensor (model 346-BCL) and a counter (model
4100/4150) are used. The sampling rate is set at lOO mVmin, the channel settings vary
with the sizes of the challenge materials.
Chapter 3 78
The system cleaning started with the rig being cleaned with 0.1 % of Ultrasil 50
(pH 4.9) or Ultrasil 11 (pH lOA) for a few hours depending on the water quality and
previous history of filtration. Then the residual detergent in the rig was washed away
with tap water. The rig was again filled with 50 litre tap water and filtered by the
Millipore cartridge filter until it was clean.
During system cleaning, the filter was replaced by a pipe and dipped in solvent
for 30 minutes. When the system had been cleaned, the filter was put back and
backflushed by air or water for several times, each time lasted 2 - 3 seconds.
Between each two test runs, the cross flow filter was also backflushed for several
times, each one lasted 2 seconds.
Chapter 3 79
The cooler was on during this operation. The Hiac/Royco sizing equipment was
used only at the end of the process to check the solids concentration.
b) Silica powder mixture (3 - 20 Ilm with dso = 7 Ilm) was used to simulate the
solids in real seawater [Knibbs. 19851. the size distribution of the both are shown in
Fig 15. The silica powder was mixed in 200m1 deionized water from the Milli-Q water
system (referred to as deionized water later) and was ultrasonically vibrated for 30
minutes before it was put into the tank.
100
~90
0
~
Ql so
N
'iij
~
Ql 70
"0
c: Iiiiii
:> 60
<Jl
<Jl
t1l 50 seawater
E
Ql 40
>
~
30
><
:>
E silica
:> 20
()
10
100
;;e
e.... 80
I
Q)
.!:l
VJ
~
Q)
"C 60
I
c:
::>
VJ
VJ
as
E 40
j
Q)
>
~
"S
E 20
1..1
::>
U
0 I I I I I I
o 5 10 15 20 25 30 35
Particle size (microns)
After the mixture had been put into the tank, it was circulated for 5 minutes in
the recycling lines to ensure that it was homogeneously distributed in the tank.
3.2.4 Membranes
a) Metal fibre tubular filters (Fairey)
Three such filters were used for the tests. Each of them has 0.014 m ID and
0.01 m2 inner surface area. The absolute pore size is 3 Ilm. The flow is fed inside of
the tube and permeate leaves from the shell side.
Chapter 3 81
3.2.5 Calibrations
a) Pressure gauges
The calibration was carried out with cleaned tap water on a weekly base.
The three gauges are the same model. When the pump is off, they all display
0, when the pump is on, the inlet valve is opened, outlet and permeate valves are closed,
they also display same pressure readings.
Due to the positions where the gauges were situated, the pressures indicated from
the outlet and permeate sides were lower than those in the modules, therefore it was
necessary to carry out pressure distribution tests for each filter to check if the displayed
value represented the real situation. This was done by fully closing the permeate valve
(B3) and fully opening the outlet valve (D2), recording the readings from all the gauges
under different flow rates (varied from 4 to 20 Vmin). If the difference between (PI +
P2)!2 and P3 is great, where PI, P2 and P3 are the inlet, outlet and membrane feed
side pressure respectively, then corrections were made. The details of the corrections
will be described in the next two chapters.
Chapter 3 82
The six channel thresholds were fIrst set at 0.7, 1.1, 2, 3, 5 and 9.8 ~m. 50
litres of tap water was cleaned with the 0.1 ~m Millipore cartridge fIlter until the total
counts of particles larger than 1.1 ~m were less than 10 per ml, the system was then
regarded as clean.
Table 6
Hiac/Royco readings vs. solids concentration
0 290 76 10 5 6 4
The lower channels which responded to smaller sizes saturated fIrst, the channel settings
were then adjusted to a larger size. The highest concentration was 15 mg/l, which was
much higher than that of seawater. The results are shown in Table 6, the particle
concentrations are in counts per I ()() m!.
The Hiac/Royco readings essentially increased linearly with the solids con-
centration for small particles. For large particles (~9.8 ~m), the counts fluctuated at
low readings. This was due to the low concentration of large particles in the silica
mixture. From the above test, the Hiac/Royco was shown to be capable of monitoring
the solids concentration in the tests.
This test was carried out only once. The Hiac/Royco sizing equipment was
self-calibrated against cleaned tap water several times a day.
c) Flow meters and chart recorder
Flow meters and chart recorder were calibrated on a monthly base against a
known volume collected in a measured time.
d) Temperature fluctuation
The experiments were usually run with 50 litres of water for two hours. The
variation of temperature during this process period was within 1 ·C and therefore the
change in permeate flux due to the temperature variation was neglected.
e) Particle shedding effect of the rig
It was necessary to investigate the particles produced by the rig itself during the
process. Only Rig 2 was tested since both rigs were made of same materials. When
the water in the rig had been purified by the Millipore cartridge fIlter, the system was
run at 251/min and 12.51/min for two hours respectively with the Hiac/Royco monitoring
the variation of particle counts.
The number of counts in a channel, between particle sizes (~m) given by the
legend shown in Figs 17 (251/min) and 18 (l2.51/min) respectively was monitored with
respect to time.
Chapter 3 84
180
160 ..- •
0.8
140
.....-- $
1.1
120
~ •
1.5
~c 100 /
8"
~
"·10 80
/ 2.0
,
9
0-
60 .I 3.0
40 ! 5.0
... --. •
20
I..~
0 I I I I I I I I I I I I
o 20 40 60 80 100 120
10 30 50 70 90 110 130
Time (mins)
120
/ -- --- --
•
0.8
100 ,
j - ---- 1.1
•
80
E 1.5
~
]I
c
8" 60 2.0
J
~
"10
0-
9
3.0
40
,./
5.0
20
~ ~
-.- -
0 I I I I I I I I I I
o 20 40 60 80 100 120
10 30 so 70 90 110
Time (m!ns)
From the above figures we can see that the rig does not produce any significant
particles in the range of 2 - 5 ~m which we are interested in, therefore, the shedding
effect of the rig can be ignored.
c) Effects of operating pressure and feed flow rate on the permeate flux rate
For each concentration, 3 sets of tests were conducted:
Transmembrane pressure by changing the flow rate with P2 fully opened, then
the effects of shear force on filtration by changing the flow rate with constant pressure.
Finally the effects of pressure on the permeate flux rate by varying the transmembrane
pressures at constant feed flow rate.
types of filter were not suitable to be tested due to their sizes or structures.
For algae with solids, Scanning Electron Microscope (SEM) was used to
investigate the form of deposit layer on the membrane surface.
c) Solids concentration
Recorded from the Hiac/Royco sizing equipment in counts/lOO mVmin, and
expressed in counts per ml;
The retention efficiency to the lipids was only investigated during each test of
the Fairey No 98 filter, lOO ml of permeate or feed was mixed with 45 ml chrolo-
fonnlmethane mixture (2: I), and the filter was submerged in 75 ml of solvent for 30
minutes. The solution was then evaporated and put in the oven at 50 ·C until its weight
did not further decrease and part of the yellow oil-like material had been dehydrated.
The lipid concentration in tap water and in the filter before fish oil was put in were also
tested. The results were 0 mg/l for both cases.
0.2
o L __ __ L_ _ _ _ ~ __ ~ ____ ~ __ ~ _ _ _ __ L_ _ _ _L __ __ L_ _ _ _ ~ _ __ J
o 2 4 6 8 10 12 14 16 18 20
Time (mins)
PTFE &befor.) P~~~~~r) .c.a.'tJ",I~
Fig 19 Flux rate of P1FE and ceramic membranes with tap water
8
~
~
c..F:
7
~
E
6
j!!
<IS
~
x 5
::>
;;:::
-
Q)
<IS
Q)
4
E
~
Q)
a. 3
$
...
0
0
In Fig 19, PTFE (before) refers to the flux rate before nitric acid was used, it is
evident that backflushing had no effect on the flux rates.
PTFE (after) refers to the flux rate after nitric acid cleaning, the flux rate was
high at the beginning and could be improved further by backflushing;
The ceramic refers to the Norton Ceraflo filter which was tested following the
same procedures, the effect of backflushing after nitric acid washing was not as
prominent as that on the PTFE filter ~.
Since nitric acid was not ideal for offshore use, it was clear that unfiltered tap
water was not suitable for direct use for the laboratory study, all the tests afterwards
were carried out with cleaned tap water if not specified.
(3.2)
The test results of Fairey and Enka filters are given in Fig 20.
The results for the Ceramic filter are shown in Fig 21. It shows that the permeate
flux rate linearly increased from 0.08 to 4.5 m3/m2.hr with transmembrane pressure
increasing from 0.07 to 1.17 Bar at a 12 Vmin feed flow rate.
The permeate flux rate of Versapor 3000 sheet membrane also linearly increased
from 2.1 to 9.2 m3/m2 ·hr with transmembrane pressure increasing from 0.4 to 0.8 Bar.
Chapter 3 90
o
4 .......................................................................•............................ ............................ .
3 .......................................................................... ··Ll··················································
o ···n··················································..................................................
.......................
o
o ~~ __- L_ _ _ _ ~ ______ ~ ____ ~ _ _ _ _ _ _L -_ _ _ _- L_ _ _ _ ~
Also shown in Fig 22 is the effect of bacldlushing with compressed air at 3.5
Bar, it indicates that backflushing can recover the flux rates to as high as 80 -90 % of
their originaL
Chapter 3 91
3.5 4l/min
•
fibre 97
3
1 •
'E
_ 2.5 fibre 98
o
fibre 99
*
CD
E
~
CD
a...
1.5
0.5f--'_
- ••**&.a.
DOElCU
0L-__~L-__~~__ -=____-=____ ____ __
~ ~ ~
o 10 20 30 40 50 60 70
Time (mins) .
Fig 22a Flux rates of metal membranes (Re 85(0)
4 8l/min ' $
fibre 97
3.5
3 fibre 98
~_
)(
2. 5
fibre 99
X
:::J
;;::: 2
~CD
E
....
CD
a... 1
ooL----1~O----2~O~--~30~--~4~O--~5~O----6~O~~70
Time (m ins)
Fig 22b Flux rates of metal membranes (Re: 17500)
Chapter 3 92
Table 7
Particle retention efficiencies of Fairey filters
Filter Flow rate Retention efficiency (%) in grade (~m)
The test result of Versapor 3000 sheet membrane is shown in Fig 23. Back-
flushing was performed using compressed air at 3.5 Bar, the duration of the reverse
flow was 1 second.
8
~
.....
.r::
NE 7
M--
--E
Q)
ca 5
6
.....
X
::J 4
;;:::
- Q)
ca
Q)
E
3
..... 2
Q)
a..
1
00 20 40 60 80 100
Time (mins)
Fig 23 Flux rate of i 10 mg/! solids (Versapor)
Chapter 3 93
The above tests indicated a reasonable flux rate, sufficient for offshore use. Thus
these membranes were subjected to challenge suspensions containing lipids (fish oil).
The literature suggests that lipid containing suspensions represent the most fouling fluids
that the membranes will have to operate on, therefore, tests with 2 mg/l solids and/or
different concentrations of lipids were carried out with four different membranes.
The tests on Fairey filter (No 98) were carried out under 12 Vrnin flow rate (Re
255(0) and 1.2 Bar transmembrane pressure. Three lipid concentrations were used: 5,
10,20 mg/l. Before the lipid was added to the tank, the flux rate with clean water, and
water with 2 mg/l silica, which was still a relatively high concentration of solids for
offshore seawater filtration, were checked. The results are shown in Fig 24.
•
water
X
2
..
2mgll
lipid
10 20 30 40 50
Time (mins)
Chapter 3 94
-c-
.s::; 6 • • • •
N'
E
<O-
S
.s
CD
~ 4 •
water
)(
x
""g" 3
2mgll
'CD" •
E
CD
2
lipid
tl.
00 10 20 30 40 50
Time (mins)
•
water
x
2mg~
•
lipid
40 50
Time (mins)
Chapter 3 95
approximately the same as the calculated values shown in column 1. The appearances
of all samples were milk-like liquids after evaporation, but they were different after
drying. For the samples from the feed, they dried and turned into white spots on the
flask wall. For the samples from the filter, they became a yellow oil with a strong
fish-oil smell after drying, further drying only resulted in dehydration without any weight
reduction.
TableS
Lipid concentration in the feed and filter
at different lipid concentration in the tank
5 5 34.8
10 13 81.9
20 25 192.4
Since the polypropylene Enka filter is hydrophobic, the membrane was wetted
with IPA before it was used and backflushed with water at 2.8 Bar during the process.
The tests with solids and lipids were all carried out under 0.7 Bar transmembrane
pressure and 12 Vmin feed flow rate. The results are listed in Table F of Appendix 3
and shown in Fig 25.
The figure shows that increase in the concentration of challenge materials did
not significantly change the flux rate, but change in challenge materials brought about
significant change in flux rate.
Although the flux rate dropped when challenge materials were added in, the flux
rate was still high: up to 0.7 m 3/m2 .hr, therefore it was a good candidate for seawater
filtration if backflushing with water is acceptable under offshore situation.
Chapter 3 96
0.9
~ 0 a
~~~;,~~··"···"-·-·-·-·-·:;~~~~{ii~~~z
.•
0.8 ..
> .~,~~.....................
".._".-.. ::::::~:;~;= .... -........... AI;:~-
0.7
0.6
- -
-.- -_.-.....
•••••• -.- -- ._ ••••• - -
-.
{""'.".. - ....c-.&.......
_- ... _.."
~.;.;~
-- _
.•..·..
• • _ . - ___ A
-..-
.,.,
_. __ . _ • • • - -
..
..' '-.... .~/ .........
_. _. - • • _________ - _ •••••• - . _ . _ • • • • __ - - __ - _. _
'
•• _. _ • • _. ___ • • • _. - - - _. ____ • • • • • • • __
0.5 L--'-_-'-----!L--L_-L----!L--'-_-'----'_-'-_-'----'_-'-_-'---'
o 2 4 6 8 10 12' 14 16 18 20 22 24 26 28 30
Time (mins)
water 0.5 mg/l solids 1 mg/l solids 2 mg/l solids
o ---6--- .... ·0 .... - -'7(--
50 tests were run with ceramic filters on Rig 2. The results are listed in Table
G of Appendix 3. The backflushing was commenced at the 48th minute for I second.
The results of test No 7, 17,25,35 and 45 are shown in Fig 26a, which were under
similar test operating conditions but different concentrations, another set of such test
results, but at higher transmembrane pressure, from tests No 10, 20, 30, 40 and 50 are
shown in Figure 26b. From the two figures, we can see that the increase in the pressure
greatly increased the flux rate. The flux rate decayed more quickly when lipid was
added in, this confirmed the conclusion by other authors that lipid is the major foulant
to seawater filtration.
Chapter 3 97
L:l ~ I:J ~
0.8 ..................................................... = ..... "". ......................... . .=........................
0.6 J. ................................................................................................................................ .
~~~ir~----------------ir~~-6-~
: ::~--,,-~:~:~;:-=:===~:---:~--~~-~:~:-
".-··'F·-=1F·=iF--:iF=:-.~.=M:··~·· ,
o L-____ ~ ______ ~ ______ ~ I __ ',. I
~~-L-------L------~ I
o 10 20 30 40 50 60
Time (mins)
wWt 2~~~~~~s 5~~!g~i~S 10.!'~~S 20_,:,:~~~~dS
Fig 26a Flux rate of ceramic filter at low pressure
3 ................................................................................................................................... .
-A..
2 .... ~~l"i''fr.~::.:::;:;::::.....................................................................................................
-----------6... ,.6
fr~~-6-----------------~
1 .:: ::~ ::::::~::::: :~:: ::::Q::::::0::::::0::::::0:", ,,@.,,:::~ ....................................................
-*-
··-·.·-:::M--:-:~:=l·-=::M.--:-:~.-=it:::
oL-____ ______L-______L
~L-
.. --:-:~
-_ _ _ _ ~L_ _ _ _ _ _ _L -_ _ _ _ ~
o 10 20 30 40 50 60
Time (mins)
WWt 2~~~~~~s 5~\jI~i~i.dS 10~~~S 20_,:,:~~~~dS
Fig 26b Flux rate of ceramic filter at high pressure
Chapter 3 98
The tests with Versapor 3000 sheet membrane were run on Rig 1 only.
Fig 27 shows the flux rates obtained from various lipid concentration tests at 80
Vmin feed flow rate and 0.7 Bar transmembrane pressure. Also shown in this figure
are the flux rates using tap water and a 2 mg/l silica concentration.
4
•
water
~
3.5
~
.s::: x
C\I •
3 silica
E
~
...
~
2.5 1mglllpd
Cl)
10
~
+
x 2 2 mg/llpd
::::I
;::
-
0
Cl)
1.5
:
<ll ~ 5 mglllpd
•
Cl)
~
E
J
~ 1
Cl)
10 mg/llp
Cl.
0.5
i
00 5 10 15 20 25 30 35
Time (mins)
Fig 27 Flux rate of Versapor membrane at high pressure
d) With algae
The tests were run on Rig I only.
Two types of membranes were used, they were Bekaertmetal sheet and Versapor
3000 polymer membranes.
The test results with two membranes are shown in Figs 28 and 29 respectively.
It was clear that changes in feed flow rate did not greatly affect the flux rate.
The permeate decayed very quickly due to the clogging of membrane pores with
algae and solids.
Chapter 3 99
1.5 ............................................................................................................................... .
1.0
Re 2500 Re 10000
Re 7500
o 20 40 60 80 100 120
Time (mins)
Fig 28 Flux rate of algae on metal membrane
~P~e~rm~ea~t~e~flu~x~r~a~re~~~~ ______________________________,
0.4
Re 12400
0.2
... ......................................... B.Ei.Z50lL.................I'I.~.1.QQ'O.() .................................
Re 2500
0.1
o 20 40 60 80 100 120
Time (m ins)
Fig 29 Flux rate of algae on polymer membrane
Chapter 3 lOO
The Enka filter had the highest flux rate of all the filters at 2 mg/l of solids and
20 mg/llipids which means it was least affected by the presence of oil in water, and the
Fairey was the lowest.
b) Operating conditions
Increase in operating pressure or feed flow rate increased the flux rate, but the
former had more effect on the flux rate than the latter within a certain range.
c) Backflushing
It is clear that backflushing is capable of restoring the permeate flux rate to 80 -
90% of its original amount, but the flux rate will drop very quickly within 2 minutes;
so that it is necessary to keep on backflushing during the whole process at certain
frequency such as 1 second per minute.
d) Membrane resistance
The membrane resistance was analysed only on the algae test results. It was
calculated according to the "cake" filtration theory as applied to microfiltration:
J M (3.3)
y ~(K+Rm)
The results, determined in in-situ, are listed in Table 9 for the metal membrane
and Table 10 for polymer membrane.
The tests indicate that the presence of algae did not affect the metal membrane
resistance, but significantly increased the polymer membrane resistance. It is also
noticeable that the polymer membrane resistance increased with increasing pressure and
decreased with increasing shear rate.
Chapter 3 101
Table 9
Metal membrane resistance
Table 10
Polymer membrane resistance
a) Clean
a) Clean
All the above resistances are membrane resistances only, i.e. not including the
cake or deposit resistance. It is clear that there are still some suspended materials in
the filtered tap water, they will deposit onto the membrane during filtration. These
deposits must have combined with the membrane to provide the additional resistance.
We learned from this test, that membrane resistance cannot, therefore, be assumed
constant and equal to that given by a clean water test, especially in the case where
particles are close to or even smaller than the pore size. The membrane resistance must
be determined in-situ, a similar situation to that of classical cake filtration. The details
of the method of building this model will be discussed in Chapter 5.
e) Fouling mechanisms
The SEM photographs of the two fouled membranes from algae tests are
reproduced in Figs 30 and 31.
It is apparent that the fouling on the surface of the polymer membrane is in the
form of a contiguous gel coating. This blocks all but the largest surface pores, and
severely restricts flow through those remaining open. The surface porosity of the clean
metal membrane is much higher than that of polymer, but the presence of low con-
centrations of inorganic materials will clog it with algae acting as a binder. In both
instances it is likely that the materials released by algae cells form a gel layer which
exerts the major resistance to the permeation.
Concentrate P1
Crossflow Filter
Air V4 P3
01
02
Seawater su F2
Thermometer 81
Centrifugal
Drain Pump
Fig 32 Layout of seawater filtration rig
The sea water used at the Test Centre is pumped from Scapa Flow which is fully
marine and the main water mass has the characteristic of the flow round the north of
Scotland into the North Sea. Plankton levels (blooms) are similar to those found offshore,
with some local coastal enhancement. Natural mineral particulate concentration is
usually very low. Since during the bloom period, the plankton found adjacent to Flotta
Chapter 3 106
often slightly precede those which cause filtration problems offshore, the experiment
was carried out over late August and the whole of September in 1990, which was not
a bloom season.
The seawater was pumped from a depth of 15 metres at the Southend pier which
is 150 metres away from the coast. The water was coarsely filtered with 80 - 100 I1m
filters to prevent seaweed or any possible large living organisms from getting into the
reservoir.
Nine samples of seawater were taken from the hose through the trial period, and
the Coulter Counter analysis for these samples are shown in Table 11.
Variation in the trial fluids was inevitable whilst undertaking field trials, but the
variation between samples show below is not substantial. More than 80% of the particles
are below 20 I1m, therefore the challenge solids used in the laboratory were close to the
distribution in North Sea seawater by their sizes. Meaningful comparison between the
filter performance can, therefore, be made.
Table 11
Seawater particle size distribution
and solid concentration during trial period
3 1.5 98 93 76 45 6
4 4.7 91 84 48 14 2
5 0.8 99 95 85 69 13
6 1.1 86 70 52 28 8
7 0.9 89 82 63 43 11
8 2.2 92 78 54 34 4
9 0.9 92 83 63 46 14
•
Chapter 3 107
c) Cleaning chemicals
Ultrasil50 and Ultrasil 11 (0.1 %), and citric acid (5%) were used to clean the
filters.
d) Precoating method
Filter aid materials (dicalite) were tried on the metal filters so asto examine the
effectiveness of precoating on fouling prevention. The system was first run at a con-
centration of 0.5 g/l and then seawater was introduced at a solids content of I mg/l. After
2 hours, backflushing was used.
Chapter 3 108
The change in Reynolds number did not significantly affect the flux rate.
All the filters had a serious flux rate decay within a short period as shown in Fig
33.
2.0
Fairey tube 12
"C" Re 21 000
.r:.
N· ~
.§ 1.5 10 3
£ Q)
Q)
a
Q)
~ 8 2'
x
><
::>
=Q) 1.0 ~
1<i
Q)
6~
E
Q)
3"
.N
tl.
4 g
0.5
Ceraflo
~ _ _ _ _ _ Re 2600 2
PTFE
Re 8500
O·h··················································· ................................................................................ .
0.3-\-·················································· ................................................................................ .
Ceratlo
Re 2600
0.2...Q ... ............................................................................................................................ .
0.1 - ................................................................................•................................................
w Ceratlo
Re 2800
,
o 20 40 60 80 lOO 120 140 160
Time (hrs)
60
All Fairey Filter Tubes 2.0
'"tl
(t)
"C"
.c: 50 14 mm ID ~
3(t)
N'
E et
",-
S 40
1.5
-
(t)
E
~
)(
precoated ~
)(
et
(t)
::>
0= 30 1.0 '3
.....,
*'"'"
E
~
c..
20 after removal of precoating
0.5
~
3
.'"
;3"
10
Re 7700
Re 17400
o 0.5 1.5 2 2.5
Time (hrs)
the following:
Good filtration performances could be achieved when filtering suspensions of
high mineral content with a mechanical membrane cleaning technique.
Transmembrane pressure had more influence than flow rate on the flux rate,
however, high pressure would result in quicker deposition and less effective back-
flushing.
Variation in the concentration of the suspended material was not very prominent
since it was the deposit on and in the membrane surface and not the solids in the bulk
flow which resisted the permeation, the higher concentration shortened the decay period,
but the flux rates at the steady-state were similar.
Since the membranes were reused after cleaning, the membrane resistance of
the same membrane varied in. different cases, it should be estimated on in-situ base.
Fouling inside the membrane was the most important problem for seawater
crossflow filtration. The major foulant was the lipid which acted as a glue combining
other low concentration mineral materials to foul the membrane internally and externally.
Chemical cleaning methods are also effective in many cases, however, two
factors must be considered before applying them: the environment, and possible change
to the properties of the membrane and materials. The chemicals used in seawater filtration
(Ultrasils and citric acid) might not be suitable to get rid of these foulants.
Precoating can provide protection to the membrane, but it may be expensive and
unacceptable from environmental standards. Precoating with sand may be an acceptable
alternative for seawater filtration.
A coarser I filter of screen type may be a better candidate than the finer
ones for seawater filtration. The use of ultrafiltration membranes would not help to yield
higher flux rates since the fouling is due to an organic gel of molecular weight proportions
Chapter 3 III
(fatty acids) - thus flux rates similar to microfiltration would be expected. However,
although the coarser membrane can reduce the possibility of building up gel bridges
across the membrane pores, the finer particles may still penetrate into the membrane
and be retained there unless a true surface filter is used.
Thus the most effective membrane for seawater filtration is one in which
mechanical cleaning (backflushing) is effective. Organic fouling is clearly inevitable
with any membrane. The required duty on oil platforms is reasonably coarse, over 50%
of the water drawn from the sea needs to be filtered at only 10 ~m. Thus an asymmetric
or surface filtering membrane with high porosity and large pore size could be used. This
could provide a sufficiently large pore to prevent complete pore blockage, or one in
which mechanical cleaning is more likely to be successful.
All the tested membranes afforded reasonable flux rates, the geometries and
types of filter did not significantly change the flux rate, this was a consequence of the
formation of a dynamic or secondary layer on the membrane surface or inside the pores.
The offshore operation with crossflow filters is feasible if the membrane fouling can be
minimised. The principle of selecting appropriate membranes is based on a multitude
offactors such as ease of operation and service, recovery ability after cleaning, membrane
packing density and robustness, and operation costs.
This work very clearly demonstrated the importance of the finely suspended
material entering the membrane filter matrix. This is the subject of Chapter 4.
Chapter 4 112
CHAPTER 4
Crossflow Microfiltration of Latex Suspensions
(Investigation of Membrane Fouling Process)
It was apparent from the crossflow microfiltration of seawater that fouling inside
the membrane is a major cause of flux rate decay. Therefore, further study was con-
centrated on this internal fouling process using well characterised latex suspensions and
membranes.
The rig was modified to use a plate and frame module because sheet membrane
is more easily investigated than other geometries, for example by SEM after the test.
Gelman Versapor acrylonitrile membranes were used, they were the same as those used
in seawater filtration except the pore sizes were slightly larger.
The module consisted of three parts: top plate, bottom plate and two flow
connectors. The structure of the these parts are shown in Fig 36. The two plates were
made of perspex so that the flow in the channels could be observed during filtration.
The connectors were made of PVC so as to facilitate connection with the pipeline.
Fig 36a is a diagram of the top plate. The fluid flows in the channels, the
geometries of each channel were 3 x 3 x 500 mm (width x height x length). There were
10 channels in the plate, but only six are displayed in the diagram because the four side
channels were not used during the experiments.
Fig 36b is the diagram of the bottom plate, three layers of different sheets were
placed on the ridges. The bottom one was a brass sheet mesh, its opening size was 1
mm; the middle one was a stainless steel membrane, its pore size was 3 Ilm, the top
one was the Versapor membrane. The lower sheets were used to support the top one.
The total thickness of the three sheets were about 1 mm, however, since they were sealed
by silicon rubber at their edges, the total thickness of the sheets increased, the membranes
intruded into the channels, and therefore, the depth of the channels was slightly reduced.
Chapter 4 113
FiWng holes
h da6 50 I 25.4
/ ~I !.-
.-. - - i i - - - - - o
M
'" ... ~ o
/////
0 0 0 o -<jt---<jt-- 0 0 0 0
.l
'"
'" T
/////// ",,,,
.... ~
Flow ch nnels
/ /.// LL/LLLLL
'",
'0
///////
LLLL
\ 000
- - - - 0 0 0 0 0 0 0 0
- - - - - -
0 0
560
5~ ~ r-f-'Ridges t.
5~
-
'"'"
....
»
",
,
~ B ~-
I
+B ~
\
~ o-
-
000
- - - -
0 0 0 0 01 0 0 '0
- - - o
_~ __?_.~..._~f.lll+-l~·:i'
l-
~l~;
Rubber seal stream/ning area
1-'" slot
B J-<o B \
" ,.... --
I
1--", ..-
,/
f-
,,
_--_ "" .... .......
/
/
I-
M
3
Fitting hole 80
Flow
.. ~~~--------~~
. . .r. . ~
o
Rubber
seal slot
" ,,
\
\
\
\
\
d=6
0
....
.-.~.-.~---.-
0)
_._-_. ~
o
M
, 11
11 on I I\
t . . . . . . . ..
"0
Flow slot \ \ I I
\ \
I
I
I
\ , I
--
I
"O •••••
3 Pressure
" port
- ~.-.-.-.-.-.-.-.-.
"
~ I
.~.-.-.-.-:-.-.-.-.
The two connectors were used to produce a flat velocity profile entering the
channels (plug flow), and also minimize the flow rate differences between the neigh-
bouring channels.
(4.1)
The temperature should not be less than 57 ·C, otherwise no reaction happened,
and the optimum range was 60 to 65 ·C.
This process lasted 24 hours, the fIrst few hours were the most important since
more than 50% of reaction occurred during that period.
The products were also fIltered and dialysed. They were stored in the glass
reagent bottles with one drop or two of phylatol in it to prevent the possible growth of
microorganisms.
4.2.3 Relevant properties of the produced latex
A total of 19 latex emulsions were made by this method, their particle size
distribution, percentage dry weight, density and zeta-potential were measured. Only
three of these latices, two with diverse particle size distribution (No 6 and 11) and the
other with relatively uniform particle size distribution (No 9), were used for the
experiments. Some of their properties are tabulated in Table 12.
a) Percentage of dry weight (wt%)
The percentage dry weight of latex was determined by the oven drying method.
b) Zeta ( ~) potential (at pH 7)
The Zeta potential of latex particles suspended in deionized water were
determined by Particle Micro-Photophoresis Apparatus (Ranker Brothers, Mark II).
c) Density
The density of latex was measured by density bottle.
d) Viscosity
The suspension was essentially an Newtonian fluid up to 58 wt% solids according
to Blake's test results [Blake, 1990] The relative viscosity of suspension could be
expressed by Krieger's equation [Krieger, 1972]
~i",,"
--.
~,,/a =(I - k" vs) " (4.2)
equipment used to monitor the filtration, the latex concentration for the experiments
was very low - less than 0.3 mg/l- the viscosity of the suspension was therefore taken
to be that of water, which is 0.001 Pa's (20 ·C).
e) Particle size distribution
The particle sizes distribution of latex was investigated by Malvern Laser Dif-
fractometer (Series 2600). Since this Malvern sizer could not provide the size dis-
tribution less than 1.2 ~m, Coulter LS130 equipment was used for No 9 and No 11
latex. The cumulative particle size distributions of No 6, 9 and 11 from theseequipments
are shown in Fig 37.
70
SO
50
, "
:: =:::::::::::::::::::::::::::::::::::::::::::::::l~ :::::1::'::::::::::::::::::::::::::::::::::::::::::::.::::::::::::::
/" I
20 _ .......................................... .J.~ .... ···t··················································................ .
/~
10 - ...................................:)'< ..•........ A. .......................................................................
I
....,....~
o L __ _~-*~~ JIi6.t:st'l 11 I 1
__~~~~----L----L~~L-----L---~
0.1 0.2 0.5 2 5 10 20 50 100
Particle size (microns)
Malvern Coulter
No 9
o
No11 NoS
---6--' ·····0····· -*""-
No11
-....
No9
-...
Fig 37 Particle size distributions of test latices
There is some discrepancy between the size distributions, especially for No 11
latex. The solid content of No 6 and No 11 latex was very low (0.13% and 1.96%
respectively), compared with that of the No 9 latex, due possibly to excess initiator
which may have stabilized more smaller particles. These smaller particles contribute
to a wider particle size distribution of the No 11 and No 6 latex.
Chapter 4 119
and permeate flow was counted by the Hiac/Royco, and compared with each other.
Only when the particle concentration of the permeate flow was as low as the cleaned tap
water, could the module be thought well sealed.
b) Inter-channel leakage test (inside the module)
When the module had been assembled, the three sheets, which were used to seal
the neighbouring channels as well as to fIlter the suspension, were pressed by the ridges
of the two plates. Since there were no sealing materials between the sheets and the plates,
and sheets them elves, it was necessary to check the possibility ofinler-channel leakage.
This was achieved by using dyed waler. After the dyed water had run along
the membrane for several hours without filtration, the module was disassembled. If
only the filter channel portions had been dyed, there was not any inter-channel leakage.
(a) 1 l/min
(b) 1.61/min
Cc) 2l/min
Fig 39 Dyed flow distribution during the minimum flow rate test
Chapter 4 123
(a) 1 Vrnin
(b) 2 Vrnin
Fig 40 Channel flow distribution test
Chapter 4 124
L=Ut (4.3b)
U=L# (4.3c)
s=~='1~ (4.3d)
Since the width of the channel was not changed by the membrane (3mm), the
equivalent height of the channel (H) could be obtained:
H=~=i ~ (4.3e)
Chapter 4 125
Table 13
Test conditions with filtered tap water
3 1.16 0.12 30
15 r-..................................................................................................................................
1 0 f-..................................................................................................................................
I I I .i
.,
10 20 30 40 50 60 70 80
Time (mins)
0.2 micron 0.45 micron 3 micron 1.2 micron
0 ---6--- ·····0-··-· -~-
The flux rate of the 0.2 ~m membrane was too low and declined quickly within
2 - 3 hours. Since it was easily fouled by filtered tap water, this kind of membrane was
not used for further tests.
Chapter 4 126
The flux rate of the 3 Ilm membrane was steady with the time but it was not
practical because No 9 latex could completely penetrate this membrane.
The flux rates of the 0.45 Ilm and 1.2 Ilm membranes were moderate and the
decline was not serious, therefore they were selected.
0.54
0.48
0.42
P2·Pp=O.04 Bar
0.36
0.18
o~---L--~~--i----L--~---i---~
o 1 2 3 4 5 6 7
Flux rate (1/min)
1.16 Vmin
0
The test to determine the minimum required pressure was carried out with filtered
tap water, different flux rates against pressures under the same feed flow rate were
measured as shown in Fig 42. They indicate that the minimum pressure difference
between P2 (outlet side) and Pp (permeate side) should be no less than 0.2 Bar and PI
(inlet side) should be greater than 0.5 Bar.
Chapter 4 127
The structures of the two flow connectors and the position of the pressure gauges
cause the real transmembrane pressure to be different from the results calculated from
the values given by Eq 4.4:
_ (Pl +P2) P
P,- 2 p (4.4)
It was found that all the three pressures increased when the outlet valve was
thronled, and the increase in P3 could be obtained from the difference between the
Chapter 4 128
displayed value on the pressure gauges and the value calculated from the Eq 4.5,
therefore, the transmembrane pressure Pt is:
Pt =M';+P3 -Pp (4.6)
where sub i refers to I (inlet) or 2 (outlet) respectively.
5 10 15 20 25
Flow rate (IImin)
Pl P2 P3
o ---6--. nm0nm
Pt
J=- (2.la)
Y Il R t
Fig 44 shows one result of Test HIll which indicates that Pt based on PI was
more linear and closer to the origin than those based on either P2 or Eq 4.4. This was
also true of membranes G and I as shown in the diagrams of Appendix 4, therefore, all
Pt in the tests were based on PI.
Jv (1/min) Membrane H
5 r-----------------------------------------------~__.
... """,,,,,-,,
4.5
fj.,;""';'"
.
-----------------------------------_ .... _.- .. _-----------------------------_._-------_ .. _------ ...----------.;, -------------
CD ..........
."
::::::::::::::::::::::::::~~::.~~~~~~:~.i~.~r.~~~.t~.~.'.::~::~~~=;.~:.~~=::.~::;;.~:::::~~~::::::::::::
4
3.5
: : : : : : : : : : : : : : : : : : : : : : : : : : : :~ ~ ~ ~ ;.:..~::~::::::.:::~~;;~:;.~;;:~:~~:::::
3
2.5
"",'" ./" DO
:::::::::::::::::::::::::::::::::=;.~~~>:::~~::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
2
1.5
6"...... ."
,..'" ... -
0.5 ::::::,~~;~~~:~:::~::'.~::~::'::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
o~~~
.........~.-..-....
__- L_ _ ~ _ _ _ _L -_ _~_ _J -_ _- L_ _~_ _~L-__L-~~__~
o 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.1 1.2
Pt (bar)
by average by P1 by P2
o --'-6--- -----0-----
The system was run in single pass mode during filtration, the cumulative
permeate volume was measured periodically and the flux rate was obtained by the
following formula:
J 1 W'+l-W'_l
(4.8)
v, S 1,.1- 1,_1
The amount of added latex suspension varied for the tests of the same membrane
so as not to saturate the sizing equipment which resulted in very low concentration by
wt % in some tests although the readings by Hiac/Royco remained high.
The numbers of latex particles in different size ranges in the bulk flow were
recorded by Hiac/Royco equipment in the unit of counts per ml, then they were multiplied
by the volume of the suspension left in the rig so that the total number of the particles
of different sizes could be monitored. The concentration of latex suspension in mg/l
was calculated by following formula:
(4.9)
In order to investigate the early stage of membrane fouling, some tests consisted
of several runs, each run finished when 15 to 20 litres of permeate had been collected,
the system was then turned into batch mode without filtration to test the pressure dis-
tribution as done in §4.4.2, after that the system was switched back into single-pass
Chapter 4 131
mode to initiate another run. Some deposit on the membrane surface may have been
swept away by the increased sheat force or backflushed by permeate during the pressure
distribution tests, therefore, the flux rate may recover to some degree.
Some tests lasted as long as 160 minutes in order to see if a deposit layer or film
could be formed under crossflow conditions and if the pore blocking still occurred after
the formation of a deposit layer.
When the permeate flux rate had become steady at the lowest possible level, the
membranes were taken out and investigated by SEM to see which was the main reason
for the flux rate decay for this type of experiment.
Table 14a
Test results of latex suspensions with Versapor membranes
Membrane Pressure Flux rate Te Flow rate Ti Latex
Test d,. PI P2 Pp Pt J. e Q Re t No Cb by
in out per trns Start End Oven Hiac
Bar 3 2
m ·m- ·hr- 1
'C I/m
-min m •1-1
~m
11 0.20 0.69 0.14 0.00 0.41 2.88 0.30 20 2.00 11224 140 W
J2 1.38 0.83 0.00 1.10 2.72 0.83 20 2.00 11224 160 W
13 2.07 1.52 0.21 1.59 3.94 1.12 25 2.00 11224 150 W
L 0.20 2.07 0.83 0.00 1.45 2.10 0.15 20 3.60 20203 180 W
M 0.20 0.17 0.00 0.00 0.09 2.10 0.15 25 1.37 7689 330 6 0.152 0.014
Kl 0.45 0.83 0.28 0.00 0.55 2.22 0.73 20 1.56 8755 190 6 0.019 0.006
K2 0.69 0.21 0.00 0.45 3.59 0.20 20 1.73 9709 130 6 0.018 0.012
K3 0.51 0.21 0.00 0.36 10.7 8.15 24 1.73 9709 20 6 0.0\8 0.013
AI 0.45 0.83 0.53 0.30 0.68 10.8 6.97 24 1.33 7464 40 6 0.015 0.017
A2/1 0.86 0.54 0.30 0.40 3.51 2.25 23 1.40 7857 60 6 0.0\5 0.030
A2/2 0.94 0.51 0.30 0.42 2.27 1.22 23 1.80 .10102 50
A2/3 1.21 0.22 0.30 0.41 1.22 0.75 23 2.50 14030 60
A3/1 1.15 0.52 0.07 0.77 1.49 0.54 23 2.45 13750 60 6 0.072 0.008
A3/2 0.83 0.60 0.07 0.64 2.31 0.07 23 1.18 6622 50
BI/l 0.45 1.21 0.33 0.52 0.26 1.67 0.64 22 2.50 14030 60 11 0.040 0.006
BI/2 1.04 0.47 0.52 0.24 2.24 1.43 24 2.00 11224 60
BI/3 0.91 0.63 0.52 0.25 3.54 1.78 26 1.17 6566 60
BI/4 1.01 0.48 0.52 0.23 4.56 2.94 14 0.83 4675 40
B2/1 1.21 0.33 0.37 0.40 4.80 2.72 28 2.50 14030 20 W
B2/2 1.00 0.61 0.40 0.41 7.86 6.23 28 1.67 9372 10
B2/3 0.87 0.73 0.37 0.43 5.21 5.78 28 0.83 4675 10
B3/1 1.17 0.90 0.33 0.70 1.19 0.67 25 2.50 14030 30 11 0.038 0.010
B3/2 1.00 0.41 0.30 0.40 1.92 1.72 26 2.00 11224 30
B3/3 0.91 0.63 0.37 0.40 7.59 5.38 28 1.16 6510 30
D 3.00 1.45 0.69 0.55 0.52 23.0 21.0 30 1.16 6510 120 W
El 1.20 2.07 1.31 0.55 1.14 24.8 22.7 30 1.16 6510 120 W
E2/1 1.43 0.59 0.77 0.23 1.75 1.35 26 2.50 14030 60 11 0.022 0.006
E2/2 1.01 0.47 0.53 0.21 3.28 2.17 30 2.00 11224 60
Fl 1.20 0.62 0.48 0.31 0.24 16.5 8.22 28 1.15 6454 35 11 0.109 0.034
F2 0.62 0.48 0.31 0.24 14.0 5.72 29 1.15 6454 50 11 0.022 0.007
F3 0.62 0.48 0.31 0.24 10.7 5.27 29 1.15 6454 70 11 0.002 0.002
Chapter 4 133
Table 14b
Test results of latex suspensions with Versapor membranes
Membrane Pressure Flux rate Te Flow rate Ti Latex
Test d", PI P2 Pp Pt Jv e Q Re t No c" by
in out per tms Start End
---:-
Oven IHiac
Ilm Bar m3·m-1·hr- 1 ·C Vm mm mgor t
G1 1.2 0.54 0.41 0.26 0.15 36.6 31.7 29 1.22 6847 15 11 0.22
G2/1 0.69 0.48 0.31 0.16 20.3 6.73 29 1.22 6847 10 11 0.22
G2{2 0.69 0.48 0.31 0.17 9.47 4.73 29 1.22 6847 20
G2/3 0.69 0.48 0.31 0.17 6.00 2.40 29 1.20 6734 30
G2/4 0.69 0.48 0.31 0.17 4.87 1.80 29 1.22 6847 30
03/1 0.69 0.48 0.31 0.20 8.47 3.33 29 1.15 6454 30 11 0.22
O3{2 0.68 0.48 0.31 0.18 6.93 2.53 29 1.15 6454 30
03/3 0.68 0.48 0.31 0.15 5.40 1.53 29 1.18 6641 40
03/4 0.68 0.48 0.31 0.17 3.73 0.93 29 1.18 6622 50
G4/1 0.68 0.48 0.31 0.17 3.73 1.20 29 1.16 6510 40 11 0.20
G4{2 0.68 0.48 0.31 0.19 2.33 0.87 29 1.17 6566 40
HI/I 0.45 0.90 0.76 0.14 0.64 13.9 11.3 29 1.18 6622 12 11 0.25
H1{2 0.90 0.76 0.14 0.61 11.9 8.80 29 1.18 6622 12
Hl/3 0.91 0.76 0.14 0.64 9.73 6.13 29 1.28 7183 16
HI/4 0.90 0.76 0.14 0.60 7.33 3.53 29 1.20 6734 20
H2/1 0.90 0.76 0.14 0.62 4.40 2.27 26 1.22 6734 32 11 0.33
H2{2 0.91 0.76 0.14 0.64 2.80 1.40 26 1.23 6903 48
H3 0.90 0.76 0.14 0.65 2.67 1.29 25 1.17 6547 130 11 0.20 0.002
H4 0.90 0.76 0.14 0.61 2.48 1.00 26 1.17 6547 130 11 0.12 0.006
H5 1.38 1.03 0.14 0.91 2.81 1.43 29 1.94 10859 130 11 0.12 0.008
H6 1.86 1.03 0.14 0.95 2.91 0.95 29 3.08 17304 130 11 0.12 0.004
11 0.45 0.76 0.62 0.41 0.26 9.04 4.93 29 0.95 5331 80 9 0.03 0.008
12 0.81 0.62 0.41 0.23 4.13 1.37 25 1.22 6828 130 9 0.03 0.022
I3 0.77 0.62 0.41 0.16 2.83 0.97 25 1.28 7161 160 9 0.02 0.003
Chapter 4 134
Te is the temperature in the tank. This was kept between 25 to 29 ·C, therefore, the
variation in density and viscosity due to temperature were neglected.
Flow rate includes feed flow rate and Reynolds numbers of each channel, the
equivalent hydrodynamic diameter of the channel was 2.98 !TIm. The Reynolds numbers
in all tests were greater than 4000, so that all channel flows were turbulent.
Ti item in Column 12 is the period of each run.
Latex item includes the latex types and their original bulk concentrations of each
test by OVEN and HIAC methods, word W refers to tests with water.
4.5.1 The particle concentration variation during filtration from Hiac/Royco sizing
equipment
Table 15 is the latex concentration of all tests obtained by OVEN and HIAC
methods. The values by HIAC were close to those by OVEN method at low concen-
trations, but much lower than those at high concentrations. This is because the
Hiac/Royco could not count particles smaller than 0.7 Jlm and only six particle sizes
were used in Eq 4.9 to calculate the concentration, therefore, the concentrations by
OVEN method were used for analysing the results from membranes G, H and I.
The results of the measurements of the particle concentrations in the fresh tap
water, filtered tap water, original bulk flow and permeates with Hiac/Royco equipment
of Test H5 are tabulated in Table 16. The details of latex suspension variation during
the test are shown in Fig 45.
It is evident from Table 16 that particle concentration in the fresh tap water is
very high and the 0.1 Jlm cartridge filter can effectively get rid of these particles. The
particle concentration in the permeate is low so that the loss of particles in the permeate
can be neglected during calculation of the bulk flow concentration.
Since the tests were run in single pass mode and the permeates were very "pure",
the concentration in the bulk flow should have increased with time, This phenomenon
is demonstrated in Fig 45a where the particle concentration in six channels increased,
however, Fig 45b shows that the total amount of particles in the system decreased.
The only reason for the loss of particles was that they had been trapped inside the
membrane pores since a filter cake did not form as shown in Fig 47.
Chapter 4 135
Table 15
Latex particle concentrations of all tests
Test Ch mgfl) Latex Water Channel settinl?:s (urn)
Oven Hiac ml litres counts/ml
No6 10 mllatex in 100 ml water 0.9 1 1.1 1.5 1.8 2.3
M 0.212 0.012 10 85 554 581 386 404 755 1327
K1 0.257 0.006 5 35 205 230 175 140 314 729
K2 0.255 0.012 8.5 60 230 263 214 303 981 1259
K3 0.252 0.012 7 50 169 194 165 217 918 1359
Chanl?:e channel settinl?:s 1.1 1.3 1.5 2.3 3 5
Al 0.201 0.018 9.5 85 149 317 1024 516 303 132
A2 0.210 0.027 10.5 90 195 282 989 913 405 200
A3 0.100 0.008 5 90 105 168 656 309 128 43
Chapter 4 136
Counts/ml
1,500 , - - - - - - - - - - - - - - - - - - - - - - - - - ,
1,400
1,300
1,200 ::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::=~;i(~::::
~-~
.:~~::::::::~;;~~~~~=~=~~::~:::::~:::~::~::::::::::::::::::::.:::::::::::::::::::::
1,100
1,000
900
800
700
600
500
400
300
200
100
0.9um
D
1.1 urn 1.5um
---6--. ····-0-····
Time (mins)
45,000
I'
.. \ .......................................................................................................................
40,000
l'x
.........~ ..............................................................................................•...........••
~--*
35,000 ""'*--"*--?E
............................... .........................................................................................
15,000
1 0,000 rr-i3-~~""!~"-i...=i~~·s·:>-i···iii··:::···:::··~···iii··f:.:··:.:.···:::··.··;.:···:··::,···.··~···:::··;.;··i···~··;···;··i··t···;··;.··~···t··~···~··il·
5,000
It was noticed that the sampling rate of Hiac/Royco equipment dropped from
1()() ml/min to 80 ml/min within 10 minutes, which led to low counts, and the counts
would also jump after adjusting the sampling rate. This resulted in a fluctuation of counts
for the six curves in Fig 45a. This error was later prevented by fixing a nozzle at the
exit of the sampling pipe and progressively reducing the pressure drop across the
sampling cell. The counts then increased steadily. The particle counts at time 0 are for
clean water, the latex was added in at the 2nd minute which resulted in the jump in the
counts.
. One of the intentions of this work was to find out the relationship between the
flux rate and the thickness of the deposits, however, due to the pore size distribution,
the particles larger than 0.7 !lm also penetrated into the membrane and were retained
there. This greatly reduced the flux rate without forming any deposits on the membrane
surface, therefore this relationship has not been quantitatively investigated by this
experiment.
Table 16
Particle concentrations in Test H5
4.5.2 The effects of the membrane pore sizes on the flux rate
Although the variations in the concentration of minute particles during the
filtration could not be observed because the Hiac/Royco sizing equipment did notrespond
correctly to the particles less than 0.7 !lm in diameter, the results of the Coulter analysis
showed that their concentration in the latex suspension was very low as shown in Fig
37, therefore, the membranes were apparently fouled by particles whose sizes were up
to the largest; membrane surface pore which\[,· as shown in Figs 48a and 49a, is about
5 !lm for membrane G which covers 80% of No 11 cumulative particle size distribution,
Chapter 4 138
and 1.7 ~m for membrane H and I which covers 40% of No II latex and 80% of No 9
latex cumulative particle size distribution respectively, therefore, considerable amount
of particles will enter the membranes during filtration which makes the assumption.,(2)
in Grace's theory valid [Grace, 1956].
Fig 46 shows the results of the permeate flux rate of tests G2/1 and Hili
respectively.
The concentrations and channel velocities for both tests were similar but test
Hill was under higher pressure. Membrane G which had a larger pore size provided
higher flux rate at the beginning, but it dropped very quickly: within 10 minutes, it
was surprisingly lower than that of membrane H. The results indicate that the larger
pore membrane is prone to be fouled at the beginning of the process due to high flux
rate which brings more small particles into the pores and leaves them there. Therefore,
Jv can not be restored by flushing the surface even if it is run under low pressure.
Jv (I/min)
4
3.5 ......... ---------------.---... --.-----.......... --.--.---------------------.----.. ---........ -- .......... ---..... --... -----.. --
2.5
0.5
o L -_ _ _ _ _ _- L_ _ _ _ _ _ _ _ ~ _ _ _ _ _ _ _ _L __ _ _ _ _ _ ~ ________ ~
o 2 4 6 8 10
t (mins)
G2I1 H1/1
o ----6---
membrane, it can be as large as I. 7 ~m, both are about four times greater than the rating
values. The rated pore size results from overlapping of the pores to provide a tortuous
flow path. Therefore, particles larger than the rated pore size will be trapped. Since
this is common to all "diffusive" type of membranes, it is essential to have a com-
prehensive knowledge on the membrane pore size distribution so as to give better
infonnation for the analysis of the test results. This test has not be carried out in this
study due to the lack of available facilities, e.g. a Coulter porometer.
All the structures of foulants in either type of filtration do not differ from each
other significantly whatever the difference in the latex and membrane pore sizes.
The pore size distribution of the "diffusive type" membrane is wide, the
membranes with different pore sizes will give similar flux rates when fouling has started,
because the membrane with large pores will be fouled more quickly than that with the
finer pores even if the larger pores had been only partially blocked.
There were filter cakes on the surface after dead-end filtration as shown in Figs
48b, 49b and 50 and the particles agglomerated, but there were no such cakes on the
surface and particle agglomeration was not so evident after crossflow filtration as shown
in Fig 47 in which most particles were separated whether on the surface or inside the
wholly or partially blocked pores.
The indented parts in Figs 47a(3) and 47b(3) are the positions of a filter ridge,
there are no latex particles on it which indicates excellent isolation between the channels.
Chapter 4 140
(a) clean
(a) clean
(2.27)
Fig 51 is the relationship between I. and P,ofTests H3, H4 and 12, I3 respectively.
These tests were not run wilh new membranes and they ran for at least 130 minutes so
that the film mighl be formed during the process. Fig 51 suggests a dependency of 1.
on P, when P, is less than 0.9 Bar. Besides:
Chapter 4 147
D
koc- (4. lOa)
x
Je (m
Irtl .hr)
1.4 r---------------------------,
1.35 ~--------------------------------------t_J2.--------------------------------------------------------------------------------
1 ~~: ::::::::::::::::::::::::::::::::::::j:::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::~~:-~:::::::
1_2 1--------- ------------ ------------ --/------------------- ------------------------------------- --- -------------- ------- -----------
1_15 I
r--------------------- -----------T------------------------------------------------------------------------------- ------------
1_1
I
r-------------------------------l----------- --------------------------------------------------------------------- -------------
I
1.05 f-------------------------------t----------------------- --------------------------------------------------------- --------------
1 r----------------------------/-------------------------------------------------------------------------H4-riJ---------------
I:. 13
0.95 f-----.-...... --------.----------------------------------------------.--------------------.---------------------------------------
Several models for panicle distribution during filtration were presented in § 2.1
corresponding to the flow resistances Rc, RpD and RAD respectively. Some blocking
models were used to analyse the test results of membranes G, H and I. The details of
the analysis are shown in diagrams in Appendix 4. Since all the four models have linear
Chapter 4 148
expressions, the experimental data were linearly regressed, if the regression line meets
the experimental data well, the model is, assumed to be valid. 'Some
results oftestG4 by these models are presented in Fig 52 for illustration. All the diagrams
with relevant models are similar and lead to the same conclusion.
b) Complete blocking model and Intermediate blocking model (Eq 2.3 for RpB)
The Complete blocking model is expressed as:
Both models indicate that the pore is wholly blocked by a single particle, but
the photographs in Fig 47 show that the pore is not wholly blocked by a single particle
but partially blocked by many particles inside the pores. The analysis results in Figs
52a and 52b also show that the Complete blocking model and the Intermediate blocking
models do not fit the experimental data. Therefore, these two models are not applicable
in this study.
c) Cake filtration model (for Rc)
The cake filtration model for normal flow is expressed as:
tIQ=A-Q+B (2.33)
where A and B are experimentally determined constants
It is usual to replace Q with cumulative vlome of filtrate (W):
tIW=A-W+B (2.44e)
It was evident in Fig 47 that there was no filter cake on the membrane surface.
The elimination of the filter cake was caused by the shear force produced by crossflow
since there were filter cakes in Figs 48 to 50 after dead-end filtration. Fig 52c shows
that the prediction by the Cake filtration model did not meet the test results very well.
However, this model fits better than either the Complete blocking model or the Inter-
mediate blocking model.
Chapter 4 149
- 2In(J/Jo)
, -__________ Complete Blocking Model ~~~~~~~_2 _ _~~_ _ _ _ _ _ _ _ _ _ _ __ ,
, .4 ------------._----.--'. ----_. --_. -.. ------.. -------- __ A -_. --- ------ -. --- _.' .---. --- •• - •• - ••• --." •• --. - - ••••••••• -- •• --- ••••• ' . -
6
................................................................................. Q.... .__l:C;;'ir"'"::"z"I... g ... 6 ...
0.8 ···································O················LJ·.. 6 ...... >~~-""~.::::.....................................
0.6
o
·········································8···· ~
,--
,,:: .................................................................
0.4
... [J ......................................................................................................
0.2
oL-~-L __ ~ ____L -_ _-L__ ~ ____L-__- L_ _ ~ ____ ~ _ _- "
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t(s)
G4/1
o __G412
-fin.
(a)
500
oL-__ ~ __- L__ ~ ____L-__-L__ ~ ____L -_ _ ~ _ _- L_ _ ~
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t(s)
G4/1 G412
o ---fi-_.
(b)
Chapter 4 150
:~:::: : : : : : : : : : : : : : : : : : : : : : : : : : : :; ~ ~: ':~: : : : : : : : : : : : : : : : : :
/"tS
240,000 ------------------------------------------,.-:---fj,----------------------------------------------------------------------
~t;.~t" I::.
21 0,000 ---------------------;;:;8"'b---------------------------------------------------------------------------
180,000 ----------fii.,,-IJ.~------------------------------- ----------------------------------- ---------------------------
6 ~
/
150,000 ,,--,,--------------------------------- ------------------- - -- --------------------------------------------------
.. _.. ____________ ______ =_-----"'D.
120,000
90,000
60,000
30,000
O~~_~_~ _ _ L_ _ L_ _L_~_~_~_~_~~
o 0_001 0_002 0_003 0.004 0.005 0.006 0.007 0.008 0.009 0.01 0.011 0.012
W (m3)
G4/1 G4/2
o ---6---
Cc)
tlW (51m3) Standard Blocking Model
330,000 , - - - - - - - - - - - - - - - ' - - - - - - - - - - - - ,
300,000 I-------.. ----. -------. --------------------------------------------. -----. ------------. -------- Ji,::::."i..-A"::ti:=- ~
1Jr-
270,000 I---------------------. -------------.. -------------. ----. ---. ------------. --::w-...A-::-------. ----.--------. ----------
.Ils-.A~
240,000 I------- --------------. ------. ------.. ------. ------. ----....,.,,-::--.. -. ---. ------. --. --. -------. -. ---- .------... -----.----
,,--~
..A--u
21 0,000 I-------.. ------------------A'".A-'"------. ------------.--------. -----. ------------. ------- .-- ----.:p: --. ---- ~
__ Ir- .J:I. ~ --r:::J
180,000 I----.;;;:;tr'.~l:\---. --------. ----.. ------------. -------. ---- ------- ------- -- -- ------ ------------------------
~--=
150,000 I----------------------------. ------. ----'-" - -
-=-=
----------. -------------. -----.. -------.. -------------------. ----
120, 000 ~ --- . =--....-------. ------. ----. -. ---.--. ------------. -. ----. -. -------------.. ----------. -.. ------. ---
90,000 1----------------------.------.------------.-.----.-.----.-------.--.---.------.-.------.------.---------------------.---
60,000 r-----·-------------------------------------·-------------------·-·-----·-------.-------------------.-------.-----------
30,000 r -------------------------------------------. ------------. ------. -------. -----. ------ --------.. -------------------------
0~_~1_~1 _ _~1_~1_ _~1_~1_~1_ _~1_~1_~
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t(5)
G4/1 G412
o ---6---
Cd)
Fig 52 Mathematical analysis of Test 04
Chapter 4 151
There was no direct indication in Table 14 that the increase in channel velocity
brought about an increase in flux rate. This was because the increase in flow velocity
only resulted in the increase of shear force on the membrane surface. Increasing the
flow velocity will not help to increase the permeate flux rate if the fouling was due to
internal pore blocking, as shown in Fig 47. It was also found that the flux rate recovered
slightly after a pressure distribution test during which the channel velocities had been
changed without filtration.
d) Standard blocking model (Eq 2.4 for RAD)
This model is expressed as:
tIW=A· t+B (2.44e)
The results from this fit the experimental data very well as shown in Fig 52d
which means pore sizes were affected by small particles adhering on to the pore walls.
This is in agreement with the photographs shown in Fig 47 where the particles inside
the pores can be clearly seen.
Chapter 4 152
if Om and/or Nmcan be directly obtained from Eq 2.44c and 2.44d by the fIrst run of the
new membrane with the rated pore size ct. as ~:
CpoTe· d;' • P, • B
o=
m
321l • (1 - E,) • p, • A
(2.44c)
512Cpo,. • Il
N = 1 (2.44d)
m 1t. S • dm3
P, Ps (1- E,) • A B
then ~ of the following run of the same membrane can be calculated with the
same om and/or Nmif A and B of these runs are known.
Where Il is the dynamic viscosity of the water (0.001 Pa's)
E, is assumed to be 50% for all runs
c.,..., is the particle concentration of the fluid inside the pores (kg/m 3
)
3
p, is the density of the latex particle (kg/m )
P, 1281l Q
(4.12a)
om N m 1td:S
which means:
(4.12b)
Om l1td:S
-=--- (4.l2c)
N m a l28Jl
Bm 1td: S
a-=-- (4.l2d)
N m l28Jl
From Eq 2.44b:
(2.44b)
we can have:
Bm 128Jl
Bi =-N --.-P,. (4.13a)
m1tdi S '
where d, is the pore size at the beginning of the ith run.
Since Bm and Nm are assumed constant, OmoNm and O"jNm are also constant.
Therefore, o"jNm in Eq 4.13a can be substituted with that in Eq 4.12c to obtain:
2 d; (4.13b)
i
d = ,ja 0
.
B· • P .
'.
The results from Eq 4.13b are tabulated in the Table 17 as dm' The values of
the rated pore sizes (d,,) for each membrane are those as listed in Table 14, i.e 1.2 and
0.45 Jlm respectively. Also tabulated are the experimental data such as transmembrane
pressure (Pt), the particle concentration of fluid in the pore (C po ..), cumulative permeate
volume (W) and the constants A, B obtained based on Grace's (1956) model. The
estimated pore sizes of clean membranes H and I obtained from Eq 4.l3b are similar to
each other and smaller than the rated values while the estimated pore size of membrane
G is greater than the rated value. It is also clear that all pore sizes of the three membranes
all generally decreased with ongoing runs during each test, they drop quickly during
the first several runs and slowly during the last several runs. There are also exceptions
between some tests such as G3, G4 and H3, where the pore size is greater than or
equals to that of previous run due to smaller values of B·P" the reason for this will be
discussed later.
Chapter 4 154
Table 17
Test results and pore size estimation of membranes 0, H and 1
o
(m
0 N
m)i 1tSp,(l-E,)d,;
4,Ja fii"P)
(Cpo"i _
Ai ""i ' .,
(4.14b)
0... and N... can be calculated with the results from Eq 4.12c and 4.14:
• •
Omi=;/(Om Nm)i 0 0 (omINm) (4.15a)
(om Nm)i
0
(4.15b)
(omINm)
The results of the above calculations are tabulated in the last three columns of
Table 17. The values of om are in the micron range which are reasonable for this type
of membrane.
It is clear that OmoNm,om and Nm differ from run to run. Therefore, it is
necessary to average omoNm, ~ and Nmfor further work.
(4.16a)
n
•
L om'
Om=i=~ • (4.16b)
•
_
LN
j=l
m· I
Nm = n (~16c)
4.6.3 Prediction of permeate cumulative volume or flux rate with process time
The validation of the Standard blocking model also makes it possible to predict
the cumulative permeate volume (W) or flux rate (J,) with process time if Om and Nmare
known. It can be achieved by three steps:
a) Predict A and B
The gradient (A) and intercept (B) in that model (Eq 2.44e) of the first run of a
new membrane can be obtained with Eq 2.44a and 2.44b with do as d i :
tIW=A 0 t+B (2.44e)
(4.18a)
B Om 12811 (4.18b)
• NmTtdfSP'i
A and B of the following run can be predicted by using the final pore size of the
current run as <1;. However, considering the effect of pressure distribution test on the
Chapter 4 157
pore size in our study, d; used in predicting A and B are those estimated values listed
in Table 17.
b) Predict W and J.
The permeate volume W vs. time t can be obtained by rearranging Eq 2.44e into
t
w., Ai·t+Bi
(4.19a)
(4.20a)
therefore,
4 Wj • Cporei
(4.20b)
where d; is the initial pore size of the ith run which is calculated from the d;.l
of the i-I th run listed in Table 17.
C pO"i is the concentration of latex suspension (by oven drying method)
in the pore. It should be equal or close to the bulk concentration (Cb,) if the pore size
is several times greater than the particle size according to assumption (b) in Grace's
model (1956).
Chapter 4 158
together with measured Jv for comparison, and predicted graphically in Fig 53.
Table 19
Prediction of flux rate with process time (m3 .m·2 .hr·')
~ Em A B t W Jv (m3.m·2 .hr·')
"-
" " " "
Yer~
t (m1n) " "
" "
10 ~~~~~~:-~~,-............ ••• -------- •• ---.- •• ------------.--.-.--.---_. 10
--..................
____ ~----- ••":!o .... '.::~.~~~ •• -.- •• ------------------- ••• -- •••••
..
[]
c ........... - o "
---------._--_. __ ...... -----_."':."::::-:--.:-_ ...... -----_._-_._ ... _-
_.. __ ... _.. _______ ~_. __ .E ... _.Cl. ______ ~~~~_~=~=~::::: . r::::.:.:::::.::..~:::::~.::.:::'_.~~~~~:,:~~~~~~~~
o o o o o o o o
.~,----------C---------",';---------~,.c-------~~ .,~--------~---------7.,.c---------,~.--------~~
-"-
I (mln) I (min)
,.L------7------~"c-----"'.;-----CN:-----CH=------!~· , ~.---------c,7,---------:~:---------:~:---------c.,
t (mln) t (mln)
~..,~
"'a" -
z: ~:::::::~:~~~~;:~=~:::::::::::::::::::::::::::::::::::::
··········0···········································.......
u ............. JJ•......•••••••••••••••••••••••••••••••••••••..•
.---_ ....................
0 0 -------
-._-----_ -
........... ........... __ ........ . :::::~,..--.c: ...... D·tl·····································
1-5 •••• __________ ~_~.o.o.o.o.o ____ ........... ~~~~~::::::: ,.•
-O-----o--'l_c
---.g__
·································::-·t:j='''''~·············
0 c
o
... ..... .... ... -_ ..................'?~ .':1••9. E.9. .D· o · o U"O ••••••••••••••••••••••••••••••••........••••..':I.• H..c:'..... ~ .
",L---------",.C---------"N----------~L----------••
I (min) I (mln)
,: ::::.~=~:~~:::~~~;~~~~~~~~~~~-.;~:-. o
•.••••••••••••.•••..•••.•....•.•••••• Q •.•••••••••••••....•.••••
"
. ...............................................:;::;:;:~=~-
occcocc
, ,L-____ ______ ____ ______ ____ _______,,
...~--------:";---------N=---------C~:---------~•.,
~ ~ ~ ~ ~"
--o
t(mln)
Test 04/2
"--o
Test Hl/1
t (min)
Chapter 4 161
,,~-----7------7-----~------~-----",o,----.-J,' "~--~C---~----7---~.c---c,c.----",,c---",.c---.J,.
-- o
I (min) I (min)
~*I~
o
•
.-.------------_._-_ .. _-_ .... __ .... -..... ------------------------ :: ::-:~- ----- --- -------------- ----- _.- --- ----_. --------- --- -----
o .....................
--
~~~~~~~~~~~~~:;:::~:;~:~:~:~;~~:=::::::::::::
0-;-;;_ o c c
3 ---_._-----_.------------------- ••• _-- •••••• _._._--------_ ••••• -.
"L-------"C-------~-------"."c-------,C.-------e~- , ,L---~----~----,c,----~"c---c,,~--~~c---cn~---~J
I (min) t (mln)
Jv (m3/m 2.hr)
,
Jv (m3(m2,hr)
, fob.
-tlitiP-a. --- ---- --- --- ------ ---- ----- ---- --- --- --- ------ ---
~ ~;~~~::::::::::::::::::::::::::::::::::::::::::::::::::
2.5 -
"'''''
, .,-,---------~-------------------------.------,--
o oOo[p r............. 00 000
··--·-····-·-·~----~-Ett--Ci··-ti·--····----···-----·-·----·
1.5
c c c
-.-.-----------.-- .. ---.--- .. -.. -- .... -------~---~---~--- ': :::::::::~=~~~==~;;.~;~:~=:~:~:~=:::
0.5 --------------------.-----------------------------------------
·.~---=~c---~.~.----~~c---~~=---~,oo:---~,~~c---~,~ ·~.----~~c----~=----:~;----G=----o,OO~---'~M:---~'••
I (mln) t (min)
Test H4 Test H5
Jv (m3im 2_hr)
,
Jv (m3lm2.hr)
" .,u_
<>--<,
2.5 c·----·----·---·····--·········--·-------------·---------------- ---~~DtlecCoJjDo--------.-----.--.----.------.- .. --.--
"
2
'"
._ttlii!_ ..... -.IJ--- --------------------.------.•.........•.•...
il'd'l ---- --- --- --- -~~: :-::-.-~_~tl929_'?cCi_ 0-- --- ------ --- ----
... _ 0 0
---- •• ------'iL~i:J~&firJ",.---.-- .... --.--... -.-.-.---... ---.-.
0
1.5
- - - - - __ 0 0 0
0 0 0 0 D 0 --.-- .. -.-----.--------.-------------.----.-----~----- ...
0
'-e-_
, ~---~~::::::::::::::::~~~~~'~~""""""""'-'"
0.5 •••• _. _____________ •____________ •••• ____ •__ •____ __=_. __ ._
-:_-;_7:::.~ 2 --------.---------------------------.--------------------------
••L----~~c----.~.----~~C----~~---c'oo=----,~~c---J,~ ·.;--------:~:--------:••;--------:~c-------~G·
t (mln) t (mln)
-'«1 PI_ t.I ..... ..,~.
e c
TestH6 Test 11
Jv (rri3/m 2,hr)
Jv (m3im2.hr)
• ,
o
C
2.S -tII- -.- --- C ---- --- -.- --- -- ---- -- -- -- ---- -- ---- --- --- --- --- ---
2 'h"'Q,,,,,,
_____ .C ____ ..0.. ______________________________________________ _
'h"'l?,\/l0
,.5 r-----.-------------.--___ .D_ -.Q...-.g...--I~f - -ii--------------- ---
o
--~~~~~::=:::::~~=::::::=::~~~~~~~~~~
,.L----~~c----.~.----~~C----=~c---~'oo=----,~~c---J,~ U.o--------"••;--------".~c-------~'~MC-------~'~
t (min) t (mln)
~od Pr_ "'~..,-
o
Test 12 Test 13
Fig 53 Comparisons of measured and predicted permeate flux rate
Chapter 4 163
to predict d; in Table 19 were based on the estimated ct.-l and operating conditions which
brought about a cumulative error and caused smaller values and quicker decrease in If;
in Table 19.
c) WandJ,
Table 19 shows that the predictions give fairly close values to the measured ones
in W or J,. This indicates that the models are applicable to the predictions of special
note is the prediction of the maximum values of W and J,.
Eq 4.19a suggests that the minimum W is zero when t is zero and the maximum
W is 1IA when t tends to infinity, which means the value of the gradient A in the Standard
blocking model will decide the value of W.
Eq 4.19b suggests that the maximum J, is 1I(SB) when t is zero and the minimum
.J, is zero when t tends to infinity, which means the value of the intercept B in the
Standard blocking model will decide the value of J,.
The so called "steady-state" of J, has not been taken into consideration in the
prediction. The flux rate is a function of the process time in Eq 4.20b, it decreases
with the time, the greater in t, the lower in J ,. This explains why the predicted W has
a maximum value I/A. But in practice, the flux rate will become steady after a certain
time.
It is clear from Fig 53 that the predicted flux rate decreases more slowly than the
measured one, this indicates that in addition to the pore shrinkage which is the major
cause of flux rate decay, there may be other mechanisms which also increase the flow
resistances during the filtration. Therefore, crossflow filtration is a very complicated
process and it is difficult to explain the whole process by a single mechanism.
The model can give better prediction if:
I) om' Nm and d" can be experimentally obtained so that A and B in Eq 4.18
can be directly deterroined, and Cpore be determined according to d". Since om' Nm and
Cpore are independent to each other, the obtained A and B from Eq 4.18 will be smaller
and di+l from Eq 4.20 will decrease slower than before.
2) The "steady-state" filtration can be taken into consideration so that the flux
rate will not tend to zero when the process time tends to infinity.
Chapter 4 165
The particle size distribution has been determined by several different sizers.
The membrane pore size distribution has only been observed by SEM due to the lack
of alternative instruments.
The experimental results showed that the particle deposition process in this study
was a type of Standard blocking model. The pore size variation due to deposition was
estimated based on that model assisted by the data from a clean membrane resistance
test with pure water.
The mathematical model based on the Standard blocking model for predicting
the filtration process in terms of permeate cumulative volume or flux rate with process
time gave acceptable results. The model can provide better predictions if the membrane
characteristics can be experimentally determined and the dependence on time can be
further modified. These improvements will be carried out in a future study.
Most practical crossflow filtration operations deal with multi-size particles in
fluids, therefore, the existence of particles which are close to or smaller than the
membrane pore sizes will inevitably cause internal pore clogging if proper prevention
methods have not been taken. Since the membrane itself cannot stop such invasion,
and crossflow can only reduce the deposit layer on the surface, it is important to prevent
the small particles from, or at least retard their speed of, approaching the membrane
surface so as to reduce the amount of particles entering the pores. This can be achieved
by means of chemical, physical and mechanical methods as described in § 1.7.3. One
of such techniques will be presented in the next chapter.
------ --------------------------------------------------------
ChapterS 167
CHAPTERS
Many cleaning techniques have been briefly described in § 1.7, the last one of
these techniques increases the shear stress at the surface of the membrane rather than
increasing the velocity of the suspension over the surface of the membrane. However,
rotating the membrane surface has certain disadvantages such as the maintenance of an
effective fluid seal under pressure in systems containing suspended solids. Also, a low
membrane surface area per unit volume of space is usually found.
In addition to increase shear force, the centrifugal field acting on the material
suspended in the resulting rotating flow may be a significant body force and. . Increase
the permeate flux. High shear and a centrifugal field force can be effected by the use
of tangential inlet and exit ports in a filter holder. Tangential inlet conditions are used
already in hydrocyclones, which separate solid mixtures in a similar way to centrifuges
but without the need for moving parts.
5.1 Test rig and experimental procedures
5.1.1 Test rig
The experiments were carried out on Rig 2 whose layout is shown in Fig 54. The
feed tank contained 0.02 m' of tap water as suspending medium. The cleaning procedures
of the rig and the tap water with the 0.1 !-lm Millipore cartridge filter were the same as
those descirbed in the previous chapters. When the total number of counts of particles
above 0.8 !-lm was less than 200 per ml prior to adding the powdered solids according
to the Hiac/Royco sizing equipment, the water was assumed to be clean.
A conventional metal membrane, Pall PSS 5, was used for this study. Its
nominal pore size cut-off was 5 !-lm. It was 0.27 m in length and 0.012 m in diameter.
The holder was uncon~entional in its use of both entry and outlet ports at right angles
to the membrane surface as shown in Fig 55. This arrangement produced high turbulence
and high pressure drop when compared to the more conventional inlet and outlet in
parallel with the membrane surface.
Chapter 5 168
P1 P3
Feed
F1 Filter holder
02 Concentrate
Cartridge filter
01
F3
B1 Permeate
Thermometer Stirrer
Centrifugal Tank
Pump
Cooler
Drain
Fig 54 The layout of test rig
Holder
Flange
Inlet Outlet
Fig 55 The configuration of filter module
ChapterS 169
Filter
!,"
!,
,,,i i'"
,, ""
,!,
Bmm
The filtration was effected on the outer surface of the membrane, in an annular
gap of 0,004 m. The use of the outer membrane surface facilitated the centrifugal flow
field, by means of tangential inlet and outlet endcaps as shown in Fig 56a which is the
end view of Fig 55, Filtration of suspensions containing suspended solids denser than
the suspending medium would, therefore, be assisted by the centrifugal flow field ..
Fig 56b shows the alternative type of endcap employed, which had the inlet at
right angles to the filter tube and is termed "normal" entry.
An additional set of experiments was conducted using a helix formed out of
o-ring material wound around the outer surface of the membrane, using a pitch ofO.022m
as shown in Fig 57. In this instance the rotating flow, and centrifugal field, was formed
by forcing the fluid to rotate around the filter along the spiral flow path. A helix might
be preferred to tangential entry because of its relative ease of construction, The endcap
employed for helix filtration was the same as that shown in Fig 56b.
ChapterS 170
'"
----11'--- _ CD _____________ .
.-4
o
o
270
Fig 57 The side view of the filter with helically wound o-ring
However, this was not an acceptable practice during filtration using endcaps
shown in Fig 56 because of the greater pressure drop associated with normal and
tangential entry to the filter holder. Hence a series of tests were conducted to measure
the pressure inside the holder at various flow rates. The procedures were the same as
those in the pressure distribution tests in Chapter 4, Fig 58 shows the measured inlet
pressure with flow rate for the normal and tangential endcaps on the filter holder, plus
that for the normal endcap with the wound helix. The pressure causing the fluid to spin
can be calculated from Fig 58 by deducting the normal and tangential inlet pressure, at
the same flow rate. The difference between the normal and tangential inlet pressure
was due to both setting up the spinning flow field in the filter, plus an additional pressure
drop due to the presence of the spirally wound o-ring, which increases fluid drag and
hence the pressure drop.
ChapterS 171
Pressure (Sar).
2.5
./.../
2.0 ...........................................................................................2::.:/:<:.......................
/;; - ..
,.',.'
1.5 ......................................................·······················~:..t?:··············· .......................
<.
1.0 ...............................................................•
.,'l
., /~ •................................•.................
/~1,ll
.......:;/
0.5 .....• , ,'"
,/
The pressure inside the filter holder, equivalent to the penneate side under no
penneate flow conditions, also depended on the type of inlet holder used, this can be
seen in Fig 59. A higher pressure was present in the case of the tangential filter endcap,
but the helical insert did not significantly alter the penneate pressure from that given by
the nonnal endcap. The outlet pressure from the filter holders remained independent
of filter endcap type, as would be expected, this is also shown on Fig 59.
The pressure drop across the membrane during filtration, i.e. the pressure
difference between the feed and penneate sides of the membrane, was calculated from
the feed flow rate and the measured pressure. The pressure on the penneate side during
filtration was always atmospheric when the penneate valve was fully opened. The
pressure on the feed side of the membrane was assumed to be that shown in Fig 59 for
a given feed flow rate. The pressure drop across the membrane could be higher than
that shown in Fig 59 if the outlet valve is restricted. Under these circumstances both
the inlet and outlet pressures were also raised, and by an equivalent amount, over that
ChapterS 172
shown in Figs 58 and 59. Thus the amount by which these two pressures were raised
was added to the filtration (permeate) pressure taken from Fig 59, to give a new value
of pressure drop across the membrane.
//
1.0 ................................................................................................,1.............. ............. .
+/
//
0.8 ..............................................................................., .L .......... ............................
///1'/
0.2
oL-~~
o 0.08 0.17 0.25 0.33 0.42
Flqw rate (m 3/s) X1000
Permea1e Side: Fi~er ou1let:
Normal Helical Tangen1ial Normal Helical Tangen1ial
• • - ........ - 0 0 t;,.
The centrifugal pump used in this study generated heat, and the original cooling
coil was not sufficiently powerful to maintain the temperature which rose from 20 to 32
·C during a 90 minute period experiment. For a limited period in time and an additional
cooling unit was employed, a stable temperature of 24 to 26 "C was maintained under
these conditions. This experimental run was repeated under conditions of rising
temperature, the results are given in Fig 60.
Between the filtrations, the membrane was removed, washed with distilled water
and backflushed with compressed air at 2 Bar.
ChapterS 173
4 .-------------------------------------------------------,
2.5
1.5
0.5L--------L--------L-------~------~--------~------~
o 1,000 2,000 3,000 4,000 5,000 6,000
Filtration time (s).
Held at Temperature Converted
24 to 26 deg C rising to 25 deg C
o --~--- o
Fig 60 Penneate flux rate decay with time and
the effect of variable temperature
20 ----- ----1--/------+-------------------------------------------------------------------------------------------------------
/1
y 1
1
,,/1 1
o ~~~____~~------------~------------L-----------~
o 4.1 7_9 10 20 30 40
Particle size (microns)
Fine Coarse
obtained at a temperature of 25·C. This is shown in Fig 60 where the flux rate (1.)
under conditions of rising temperature has been converted to one equivalent to that at
25 'C (125) using the following equations:
Ile = 10-3 • 10(0.201844-0.019)
(5.1)
(5.2)
It is often assumed that the membrane resistance remains constant and equal to
the clean water value during filtration, thus any increase in resistance during filtration
must be due to the deposit. This approach is not valid in conventional filtration for the
estimation of filter cloth resistance, and it is unlikely to be accurate in crossflow
microfiltration processes in which the suspended particle size is close to or finer than
the pore size of the membrane such as those described in the previous and present
chapters. Therefore, the membrane resistance under these circumstances must be
calculated in-situ, just as it must be for conventional filtration.
Chapter 5 176
15
,///'
/
/,/
,
initial rate
.
............ -----------------------------------------),------------------------------------------------------------ -----------
,,
/
10 ...... ------------------~,~~/'---------------------------------
/
,/
5
-----~~~~/'----------
o __-------L------~--------L-------~-------L------~
o 1,000 2,000 3,000 4,000 5,000 6,000
Time (5)
Fig 62 Cumulative permeate volume with time and use of
initial rate for membrane resistance
Membrane resistances were calculated for all the filtrations by this method, these
are given in Tables 20 and 21 for the coarse powder, and Tables 22 and 23 for the fine
powder at different concentrations.
ChapterS 177
Table 20
Membrane resistance at 1.5% solid concentration (Coarse powders)
U P, R,. p+ File
J. Rc I
m/s m /m2·hr
3
Bar 109 m· 1 109 m· 1 Bar code
IU_I; ,I .<i".n
1.52 0.290 0.204 204 204 0.162 HF
2.08 0.416 0.441 3.1 4.0 0.337 HE
2.65 0.551 0.492 2.1 4.0 0.422 HC
2.65 0.543 0.492 2.3 3.8 0.409 HD
3.22 0.757 0.667 1.9 4.1 0.588 HA
3.22 0.639 0.667 2.1 4.9 0.580 HB
3.22 0.596 0.667 ? n 5.6 0.594 HO
Normal endcao
0.66 0.343 0.170 1.1 2.2 0.166 NN
0.66 0.287 0.176 1.4 2.8 0.164 NO
0.66 0.427 0.269 1.2 3.0 0.259 NO
0.66 0.489 0.476 1.5 5.1 0.446 NP
0.91 0.527 0.282 1.1 2.5 0.276 NK
0.91 0.363 0.299 1.6 4.0 0.273 NF
0.91 0.567 0.343 1.2 2.9 0.331 NL
0.91 0.653 0.557 1.5 4.3 0.518 NM
1.16 0.578 0.456 1.8 3.5 0.402 ND
1.16 0.465 0.456 1.8 4.8 0.410 NE
1.16 0.438 0.456 1.9 5.1 0.407 NH
1.16 0.519 0.640 2.1 6.2 0.567 NI
1.16 0.565 0.847 2.5 7.6 0.736 NJ
1.41 0.608 0.624 1.8 5.1 0.564 NC
1.66 0.694 0.880 2.1 6.5 0.782 NA
lfifi OfiRO ORRO 2.1 fi7 n7R4 NR
I~. .. ,
0.66 0.452 0.231 1.3 2.1 0.216 TE
1.00 0.650 0.461 1.7 3.1 0.410 ID
1.00 0.677 0.720 2.2 5.0 0.620 TN
1.00 0.600 0.581 1.7 4.8 0.526 TM
1.00 0.572 0.461 1.9 3.6 00403 TL
1.33 0.818 0.839 2.3 4.7 0.714 TI
1.33 0.814 0.749 1.9 4.4 0.666 TH
1.33 0.792 0.977 2.3 6.0 0.843 TK
1.33 0.849 0.750 1.8 4.2 0.672 TC
1.33 0.961 0.977 2.0 4.8 0.856 TJ
1.49 0.940 0.963 1.8 5.1 0.869 TF
1.49 0.962 1.018 2.2 5.0 0.878 TO
1.49 1.020 0.949 1.8 4.5 0.851 TB
140 1 nOl () 01>1> ')1> 1.1 077? TA
Chapter 5 178
Table 21
Membrane resistance at 4% solid concentration (Coarse powders)
U J. P, R", Rc ,
p+ File
m1s 3
m /m 2o hr Bar 10" m·' 109 m·' Bar code
Normal endcap
Tangential
Table 22
Membrane resistance at 1.6% solid concentration (Fine powders)
le P, Rn p+
U Rc I File
Table 23
Membrane resistance at 3% solid concentration (Fine powders)
p+
U Je PI R". Rc I File
Also shown in these Tables is the deposit resistance (Rc) which was calculated
by applying the Darcy's law after equilibrium had been reached. The two resistances
due to the membrane and the deposit are assumed to be additive, thus:
(5.3)
where subscript m refers to the resistance caused by membrane and its variations.
By rearranging and substituting in Darcy's law gives:
(5.5b)
(5.5b)
The combination of Eq 5.3 to 5.5 provides the following expression for total
pressure drop across the membrane and deposit based on the. normalised membrane
resistance (R~), this is the corrected membrane pressure (P,+) in Tables 20 to 23:
Chapter 5 182
(5.6a)
(5.6b)
The pressure across the membrane as those shown in Figs 63 (low solids con-
centration) and 64(high solids concentration) are the corrected values, i.e. these should
be the flux rates achieved if the membrane resistance was consistently Ix 109 m· l •
5.2.3 Effect of filtration pressure
The equilibrium penneate flux rate was clearly pressure dependent, up to a
pressure across the membrane of 1 Bar. The rate of increase in flux rate with pressure
was, however, decreasing and it was possible that the system became pressure
independent at higher pressure. Equilibrium penneate flux rates were higher when
using the tangential endcaps, i.e. with rotating flow, despite the difference in particle
sizes and concentrations tested as shown in Figs 63 and 64. The helical module also
provided increased values of equilibrium penneate flux rate over nonnal module, for a
given pressure as shown in Fig 63a.
5.2.4 Effect of shear rate
Figs 65a and 66a show that flux rate was substantially independent of shear rate at
constant pressure for the nonnal module. There was however, an underlying relation
between flux rate and transmembrane pressure. Figs 65b and 66b are for the tangential
module and some flux rate dependency with crossflow velocity can be observed.
There is some degree of spread on the experimental results shown in Figs 65 and
66 but, nevertheless, it is evident that the membrane endcaps did have a considerable
influence on the filtration behaviour of this material. If the flux rate was shear rate
independent, over this limited region, then the additional flux rate given by the helical
or tangential mode of operation must be due to the centrifugal force field.
ChapterS 183
..
...__..--i
--_._._.-----.--------_._-----------_ ..... _----_._ ..... --.-----.- ... -.. -.. --------------.-.------.---
----
-........~::::~-~- ...--.- .
0.8
0.6
..
--_ ••••••• _-_ •• _-------.-----_ ••• _-----_ ••••••>""":":::: ••••
/
/
._--
.6...---
·..........................,.......................................... ·~-....o· .. ,·........
---
-
{;
0
/
/
0.4 -----........--.---... -~-:..-/ -.................................................................................................
,/
,-
""",,-
0.2 _._--",. --- ... ---------------_ .. _---_ ....._--_. __ ..__ .....__ .. _............--_ .... _--- .. _-----_._-----------.... _------_ .... ----.
o L -________L -_ _ _ _ _ _ _ _L -_ _ _ _ _ _ _ _ ~ _ _ _ _ _ _ _ __ L_ _ _ _ _ _ _ _ ~
ChapterS 184
. --
•...••.••.•.•_______ ••.. __ •••• _____ •••...• __ .••.•.•••..•...••••.•..••..•.•••.•..•.• _______ ••••• ___ ••.. ___ • __ "":,:;-;_:0::': ...
-----;
---- 0
0.8
0.6
.: . : : :.: : :.: . : . .:.: . . .: : .: : : :. ~~~;;~~~~~~~~=~. :::~.:.::.::::. : : .: :.:
.-
0.4
........... -- --
-_.............. ..------ ........':'::.........................................---_ .... --_.... _-----_ ..........................__.....
0.2
.-,,,/'
----
.. -.-.r~~---------·--··-···············-·-·········------.-.----.---.----- .... --...................... ---...... --... -.-------.
o L __ _ _ _ _ _ ~ _ _ _ _ _ _- L________L __ _ _ _ _ _ ~ ______ ~
~ T~~';~~~I
...................................................................................................... =~:::.:...~.;.--~':'.::.::.~.
0.8
.---- ..... -- ....... -...... -... -.. -..... -.- ...... ~.-::..........................................................................
0.6
.."'.. ... ...
.;
0.2
0.8
.
...........................................................................................................•.........'-.........
-------------
...... __ ._. ___________ ... _____ .. ______ ...... _... _ _.".______ l:l ____ .____r-.:7.-:::::::=. ___ ...____ ......._
...........
0.6
A" rr_-------
0.4
-----e-
u 0
0
·················z~"'.JJi.::::::···························· ..............................-.............................
"" ........ 0
0.2 --,.t:-:-~.---.----.---.-.--- .... -----.. -...-.. ---.--.-.---... -..• ----.---------_._----_._------... ------.. --....•.. __ .__ .•..•.....
"
o~------~--------~---------L--------~------~
o 0.2 0.4 0.6 0.8
Corrected transmembrane pressure (Bar)
Crossflow velocity (m/s)
0.66g.5%) 0.912..5%) 1.16\j.5%) 1.66~.5%)
.............................................. :,~~~.~~=====».-
0.8
0.6
....................................................................................................~k-;>-_~c=~.
0.8
0.6 -----
....__ .............................--- .. -- .. -------- .. ---- .. -------------.---------
0.4
0.2
o L __ _ _ _ _ _ ~ _ _ _ _ _ __ L_ _ _ _ _ _ _ _L __ _ _ _ _ _ ~ ______ ~
Flux rate is usually a function of crossflow velocity or shear rate, the lack of
such a relation in the case of the normal module could have been due to the very high
turbulence induced by having entry at right angles to the axis flow, in addition to the
relatively short filter tube length. Another reason for this effect could have been the
large amount of fines which were smaller than the nominal membrane pore size. Thus
a substantial part of the deposit resistance was due to material depositing inside the
membrane structure and therefore, protected from the shear induced by the crossflow.
5.2.5 Effect of particle size, concentration and centrifugal acceleration
In the particle-fluid systems the distinction between free and hindered systems
is usually drawn, based on the solid concentration of dispersion. The threshold between
them is often assumed to be approximately 1% by volume, but it is a function of the
suspended material. The concentrations of different particle sizes employed in the
study were chosen to be below and above this threshold, to test the application of
centrifugally induced anti-fouling of this membrane under both of these operating
conditions. Particles influenced by a centrifugal field force and under free and hindered
conditions are shown schematically in Fig 67.
Vs
.....
V
1) Free dispersions
The drag force (Fo) on a freely dispersed panicle can be calculated from Stokes
law:
(S.7a)
(S.7b)
dx
1. dt (S.7c)
The above equation can be used to estimate the liquid flux rate towards the
membrane that must be exceeded before panicles move in the direction of the membrane.
At lower flux rate panicles will move outwards, if they are denser than the supporting
fluid, due to the action of the centrifugal field force. Thus this represents the minimum
flux rate that should be obtained from a membrane incorporating centrifugal separation.
It is extremely difficult to estimate the angular velocity inside a centrifugal
separator in order to apply Eq S.7c. Conservation of angular momentum is sometimes
used in hydrocyclone investigations, but it is often found necessary to introduce empirical
coefficients into the equations. An alternative approach is to estimate the centrifugal
acceleration at the membrane surface using a rearranged form of Eq S.7c:
2 18 ~l.
XOl =d;(p,-p) (S.8)
ChapterS 189
2) Hindered dispersions
In hindered dispersions a force balance can be constructed over a laminar layer
of suspension, instead of considering individual particles. The centrifugal field force
is again balanced by the liquid drag force, if there is no net particle motion and the forces
due to inertia and gravity can be ignored, then:
If the particle layer remains in a stationary orbit, i.e. does not move towards or
foul the membrane, then the solid velocity is zero, i.e. V. = O. Therefore:
dP ~
-=--(i-C)V (5.l1b)
dx p.
C x ol(p, - p)p.
I.= V = ~(1-C) (5.1 le )
p. can be calculated from various models, one such is Happel and Brenner [1965]:
If the permeate flux rate is dominated by the flow resistance through the most
concentrated laminar layer, which likely to be adjacent to the membrane surface, and
this layer is assumed to have a porosity of 50% then the permeability of this layer is
1.4xlO- 13 (m2 ) by Eq 5_13.
Figs 63 and 64 also show that solid concentration did not significantly affect the
permeate flux rate, over the limited range investigated.
Fig 68 is the relation between the equilibrium permeate flux rate and corrected
transmembrane pressure with tangential endcap at different axial velocites and particle
sizes at low and high solid concentration, respectively. In both cases, the permeate
flux rate of the fine powder at low velocity is higher than that of the coarse, but lower
at higher velocity.
0.6
0.4
0.2
2
Equilibrium flux rate (m'/m tu)
1.2 . - - - - - - - - - - - - - - - - - - - - - - - - - - - ,
6. ....
0.6 :-~~:~:=:.~:;=~~~~;:~~=~~i::::
,... ... ...,-
,,' .....,-
0.6 ..,L.--_ .... __ •.••• -•• -_ ... __ .. •••••••
0.4 //r'c'::~~~:~:~=~~~~::===
0.2 :.:.:~ .. -.-----------.-.-....... -.-.---------.-.. -..... -----------.---.... -----...... ----------.... ----... ----.. -._----------_.... .
Table 24
Conditions of membrane surface according to models
based on free and hindered dispersions
towards the base of the module where the exit was located. The discrepancy between
theoretical and deduced centrifugal acceleration, and the information obtained by visual
observation suggest that very careful design of the filter module must be made in order
to maximise the benefit due to rotating flow.
5.2.7 Depth of the deposit
The average depth of the deposit on the membrane surface can be calculated
from the membrane deposit resistance shown in Tables 20 to 23, the deposit permeability
estimated from Eq 5.13, and
(5.15)
Deposit resistance can be seen to vary from;, 2. I to 8.4 X 109 m·t, in Tables 20 to
23. The deposit depth corresponding to these resistances were 0.05 to 1.2 mm,
respectively. A deposit of approximately 1 mm was measured, with a significantly
tapering shape; less deep at the feed end, much thicker at the outlet as shown in Fig 69.
Calculated values of deposit permeability, resistance and, therefore, thickness appear
to be in reasonable agreement with visual observation.
5.2.8 Energy efficiency
It is clear that the permeate flux rates were enhanced by the use of rotating flow
on the membrane surface. The effectiveness of this technique can be evaluated by
considering the energy input required by the normal and tangential filters. Both filter
systems used the same experimental rig, thus Bernoulli' s equation can be applied using
the filter module entry and exit conditions of pressure and velocity. By neglecting
energy terms due to internal, mechanical and static pressure, Bernoulli' s equation for
energy per unit mass can be written as:
l!J> U2
-+-=A (5.16)
p 2
Multiplying Eq 5.16 by the mass flow rate gives the rate of energy change with
time, i.e. the power used by the system.
The pressure drop of the filter module and the fluid velocity in the module feed
pipe were used in Eq 5.16 to calculate the power requirement for the equilibrium flux
rate given in Tables 20 to 23. The results are plotted in Figs 70 and 71 foriow and high
solid concentrations respectively.
ChapterS 195
0.8
o ~~
~~~~~~~~ 0
0.6 ........ ---0----... --;....: ........... .:::: .............. -.--.--------.... -----... -----.------.. _-_. __ .......... _-_ ..... -
o .' .~/~~~
o IX······· ..............0:>
0.4 . 9·. ··~;. .O:~~--------·-·-·-·-····-······················ ......--....................--------..---------------.--------.------
..,. .tjt'
0.2 / _ _ _....L.._ _ _ _" -_ _ _...L._ _ _- - '_ _ _ _...L._ _ _- - '
L..:.
o 10 20 30 40 50 60
Power (W).
Normal Helix Tangential
o ---13--. · ... ·6.....
Fig 70a Equilibrium flux rate as a function of power requirement (1.5% coarse
powder)
..................................................................................................................•.............
0.8
o6
_~~---
.. -.... --.. -.. -.--.--.....-~::.:::------.
~~--~~.
0
. ~-----Lf---~-
AA
.... --...... -------... ---... -..... ---.--...........•... •;I_~~.":.7.:... _.. ______ .__.------_.
--------. . .
·0···_·---_·_-·-··
0.4
.
-----
""""" ................................................................................................................... .
... ,......
/
0.2 ................................................................................................................................ .
o 10 20 30 40 50
Power (W)
Crossflow velocity (m/s)
NU6 NUl N1.S TU6 Tl.32 Tl.S Normal Tangential
0 t; 0
• A
• --- -----_.
Fig 70b Equilibrium flux rate as a function of power requirement (1.6% fine powder)
ChapterS 196
1 _ ...........................................•.............•......•.......•.....•.•....•.........•...........•......•••.............
6t--
, -------~----
0.8 _ ..................................................... ·······················~'=:;It-'"':-:····················o···· ..........
--_----- A 00 0
: ~~~':':.o:~:~::::
/
"",,,,,,,,,,
o 10 20 30 40 50
Power (W).
Normal Tangential
o ---6--.
Fig 71a Equilibrium flux rate as a function of power requirement (3% coarse powder)
2
Equilibrium flux rate (m7m hr)
1.2,......:-------------------------,
.~
0.8 ...........................................................•......... :;,,~~-~---:-~ ...........Q................... .
D _--a------ 6
0
0 10 20 30 40 50
Power (W)
Grossflow velocity (mls)
NU6 N1.41 N1.S TU6 Tt.32 Tt.S Normal Tangential
D 6 0
• • • -------
Fig 71 b Equilibrium flux rate as a function of power requirement (4% fine powder)
ChapterS 197
Figs 70 and 71 demonstrate that for the coarse powder, at high power inputs or
for high equilibrium flux rates, it was more energy efficient to the filter with tangential
endcaps, at low flux rates or power inputs, the normal filtration was more efficient;
for the fine powder, filtration with tangential endcaps is always more efficient than with
the normal ones.
A common alternative method of comparing energy requirement for crossflow
filtration is to calculate the energy required to produce 1 m 3 of permeate. This can be
estimate from Figs 70 and 71. For example, Fig 67a shows the values for the flux
rate of 0.82 and 0.68 m 3/m2·hr for the tangential and normal filtration respectively at the
same power input of 30 W. Thus the time taken to produce 1 m 3 of permeate on this
filter (0.01 m·2) would be 122 and 147 hours, respectively. The energy required would
therefore be 3.66 and 4.41 kW·hr/m3 for the tangential and normal respectively. Thus
the extra energy required by the normal filter is 20% compared to the tangential one.
CHAPTER 6
Conclusions and Recommendations
During cross flow microfiltration there are many resistances to the permeate flow,
these were qualitatively described in § 1.7.1. A universal filtration theory that adequately
accounts for the importance of each of these resistances in every filtration undertaken
is unlikely to be developed. The filtration engineer has, therefore, to exercise some
discretion over the mathematical modelling based on his observation of experimental
data. In microfiltration film models, which were developed for ultrafiltration, are
often found to be inapplicable. Cake filtration models are often found to be applicable
but only when in-situ membrane and cake resistances can be calculated and, of course,
when filter cakes are formed on the surface of the crossflow microfilter. If cakes are
not formed, it may be possible to model the flux decay and equilibrium flux period by
filter blocking models.
In this study a real process fluid, seawater, was filtered on several different types
of microfiltration membranes. Manufacturers claimed that their membrane material
would be superior to the others. This was not found to be the case, as all the membranes
were prone to foul both internally and externally. External membrane fouling was by
means of a cake which built up on the surface of the filter, such a deposit could be
mechanically removed by backflushing with air or filtered water. Thus good average
filtration flux rates could be maintained under such circumstances. After each backflush,
however, a small amount of retained fines could enter the membrane thus long term
flux decay is inevitable. Ensuring a surface only deposit with all membranes meant
the use of filter aids to raise the suspended solids content.of the seawater to one sufficient
to initiate a cake. If a filter cake did not form on the filter surface, penetration of the
membrane was possible with severe consequences on filtration performance.
The photographs of membranes used for seawater filtration by SEM showed that
an organic material (lipid) acts as a binder on the inorganic debris. If such material
enters the membrane structure, irreversible fouling follows. Hence there is a paradox
that effective crossflow microfiltration is only possible when filtering concentrated
suspensions of solid material, using periodic backflushing. This is quite the opposite
of effective dead-end microfiltration on cartridge filters when rapid blocking and
Chapter 6 199
increasing pressure drop occurs under such operating conditions. Crossflow micro-
filtration was considered to be an improvement on cartridge filtration for seawater
filtration duty and this is clearly the case only under the conditions described above.
When filtering low suspended solids, cartridge filtration is preferable. Thus the two
technologies are complementary: crossflow filtration at a very coarse particle size, say
3 to 10 microns, followed by fine filtration in cartridges. During an algae bloom period,
the crossflow filters would protect the cartridge filters, during other periods the latter
filter would perform adequately. The seawater filtration work demonstrated that
crossflow membrane fouling could be due to particulates, organisms or a mixture of
both, and could be effected inside or on top of the filter.
Modelling such a system is beyond the scope of present understanding of the
process. Most theories predict the "equilibrium" flux rate and how it varies with
operating conditions such as flow rate and transmembrane pressure. Few, if any,
models consider the deposition of solids inside the membrane matrix. This was
obviously a significant effect in the seawater filtration study. Some work on blocking
models did exist for conventional filtration and for non-Newtonian fluid crossflow
filtration, mainly due to Grace (1956) and Hermia (1982). An investigation of this
was conducted using latex particles, prepared during this study, of various surface
properties. The membrane studied was an acrylonitrile type (Versapor) of nominal
rating between 0.45 and 1.2 microns. The actual pore opening sizes were in considerable
excess of these nominal ratings and, therefore, internal blocking or fouling was apparent.
The models, coupled with a mass balance on the deposited solids, were capable of
modelling the flux decline period as well as the initial and equilibrium fluxes. Thus
this approach is an important step forward when modelling filtration processes,
involving low suspended solids concentrations, in which the flux decline period is a
substantial part of the filtration cycle. The models show considerable promise but
further work is needed to enable them to be applied with confidence and with minimal
amount of laboratory testing. One noticeable factor which would assist in the full
characterisation of the membrane material used would be the provision of a Coulter
porometer. Such an instrument provides an effective pore size distribution of the
membrane material and this could be very important when combined with the particle
Chapter 6 200
size distribution of the fouling material. Such a facil~ty was not available in this study,
hence a nominal pore size was used in the modelling work and the results illustrated in
Fig 53 could be improved if the above approach is adopted.
The Standard blocking model predicting flux decay described in Chapter 4 shows
better accuracy when correlating the 0.45 I1m membrane performance than the 1.2 I1m
membrane performance. One point wonhy of note was that during the operation of the
filter, the calibration of the flow and pressures were checked several times by switching
off the permeate valve. This might have had the effect of dislodging particles which,
presumably, is more likely with the coarser membranes. The calibration check was
later found to be unnecessary and should not be repeated in future runs investigating the
permeate decay period due to internal membrane fouling.
Finally, as the membrane fouling can be due to chemical, physical, and biological
means, it would be appropriate to test anti-fouling techniques which can combine these
phenomena. For example, microfiltration incorporating rotating flow and electrical
(DC) cleaning: the foul ant is physically discouraged from entering the membrane and
the periodic application of a DC field is used to generate a local acid environment within
the membrane to chemically, or biochemically, remove the trapped species.
Nomenclature 1
ALPHABETIC
A,a,b,B the constants, their values varied according to the applied
fonnulae
C concentration (kg'm-')
CF crossflow
d diameter (m)
D diffusion coefficient (m2.s-')
D/x mass transfer coefficient represented by k later (m'.s-')
De eddy diffusivity function
(e/d) equivalent roughness of the wall
f Fanning friciton factor
F force (N)
F. CP modulus C/Ch (in Eq 2.l4b)
H height (m)
ID internal diameter (m)
J flux rate [usually in (m"m· 2.hr·')]
In Colburnj factor (mass transfer in Eq 2.31)
k mass transfer coefficient (m·s·')
k" crowding factor (the inverse of the maximum volume
fraction of the particles in Eq 4.3)
k., distribution coefficient for the solute
L length (m)
m mass (kg)
m" number of bursts per unit area (m- 2 )
M molecular weight (kg'mor')
MF microfiltration
N number of total particles one the surface at time T, (m-2 )
No original number particles per unit area (m-2 )
N, number of particles between bursts (m· 2)
n compressibility factor or power index of non-Newtonian fluid
Nu Nusselt number
p penneability (m2)
P applied pressure (Pa, Bar or psi)
Pr Prandtl number
Q penneate flow rate (m'·s·')
Nomenclature 2
SUPERSCRIPTS
+ nonnalized value
average
* wall friction
rate
o
notes to ~P - ~n = 0
SUBSCRIPTS
B burst
b bulk flow
C centrifugal
c cake layer
D drag
e equilibrium status
f foulant
g gel layer
h equivalent hydraulic
L lift force or velocity
I boundary layer
latex latex
m membrane
0 original condition
pore pore
r ratio
rela relative
s particle
seed latex seed
t total or transmembrane
v penneate
w wall
W van der Waals force
water clean water
(J surface tension force
~ zeta potential
Nomenclature 4
GREEK
a dimensionless funtion of n in Table 5b
13 parameter in equation 2.56c
y fluid shear rate at the membrane surface (S·I)
Ll difference
J.1 dynamic viscosity of the liquid (Paos)
/) membrane or cake thickness (m)
er surface tension coefficient (Nom· l)
1( 2m2/(m+l)(m+2) m=f(Fg) (in Eq 2.14b)
f( 13) result of a numerical integration involving the undisturbed
velocity profile and the Green's function.
't shear stress (N om· 2)
T) efficiency
u partial molecular volume
E porosity
p density (kg om·3 )
IT osmotic pressure (Pa)
A correction factor for the drag force on a spherical
particle in a concentration suspension
v kinematic viscosity (m2os·l)
e temperature in 'C
(0 angular velocity (rad·s· l)
1;, zeta potential (V)
References 1
References 5
References 11
Hughmark G A (1971) "Heat and Mass Transfer for Turbulent Pipe Flow" AIChE J
17(4) pp902-909
Ishii K, Hasimoto H (1980) "Lateral Migration of a Spherical particle in Flows in a
Circular Tube" J Phys Soc Japan, 48(6) pp2144-2155
Jackson J M, Landolt D (1973) "About the Mechanism of Formation ofIron Hydroxide
Fouling Layers on Reverse Osmosis Membranes" Desalination 12 pp361-378
Jaffrin M Y, Gupta BB, Blanpain P (1990) "Membrane Fouling Control by Back-
flushing in Microfiltration with Mineral Membranes" Proceedings 5th World
Filtration Congr vi pp479-483 Nice, France
Jaouen P, Bothorel M, Quemeneur F (1990) "Membrane Processes Utilizations in
Fishing Industries and Aquacultural Farming" Proceedings 5th World Filtration
.Qmgr vi pp523-535 Nice, France
Japanese Patent Application "Manufacturing of Microfiltering Materials" (Kokai Tokyo
Koho) 61-111102 29 May, (1986) 3p
Johnson J N (1986) "Crossflow Microfiltration Using Polypropylene Hollow Fibers"
Fluid Filt: Liquid Vol 11, ASTM STP 975 pp15-26
Johnson Jr J S et al (1966) in «Principle of Desalination» Chpt 8 p345 Academic,
New York
Jonsson G, Kristensen S (1980) "Membrane Filtration of NSSC-Waste Liquor"
Desalination 32(1-3) pp327-339
Jonsson G (1984) "Boundary Layer Phenomenon during Ultrafiltration of Dextran and
Whey Protein Solutions" Desalination 51 pp61-77
Kaiser D (1983) "Filtration ofInjection Fluids" Oil, Gas & Petroleum Equipment July
pp16-26
Karnis A, Goldsmith H L, Mason S G (1966) "The Kinetic of Flowing Dispersions:
I. Concentrated Suspensions of Rigid Particles" J Coli Interface Sci, 22 pp531-553
Karnis A, Goldsmith H L, Mason S G (1966) "The Flow of Suspensions through Tubes
V - Inertial Effects" Can J Chem Eng 44(1966) pp181-193
Karpov I N, Zhuzhikov V A (1981) "Mathematical Description of a Process for
Separation of Suspensions by Filtration" Theo Found Chem Eng 15(1) pp79-83
Kavanagh P R, Brown D E (1987) "Crossflow Separation of Yeast Cell Suspensions
Using a Sintered Stainless Steel Filter Tube" J Chem Tech Biotechnol 38
ppI87-200
Kawase Y, Ulbrecht J J (1982) "Turbulent Heat and Mass Transfer in Dilute Polymer
Solutions" Chem Eng Sci, 37 ppI039-1046
References 12
Wood D, Petty C (1983) "New Model for Turbulent Mass Transfer near a Rigid
Interface" AIChE J, 29 ppl64-167
Yaeger S "Trends in Semiconductor Ultrapure Water for Final Membranes" The 1987
5th Annual Membrane Technolo&ylPlannin& Conf pp13l-138 21-23 Oct
Cambridge, USA
Yan S H, Hill JrC G, Amundson CH (1979) "Ultrafiltration of Whole Milk" J Dairy
Sci, 62(1) pp23-40
Yasminov A A, Gleizer V, Volodin V F, Ryabenko EA (1990) "Intensificztion of
Microfiltration Processs in the Ultrafiltration of Fluid" High Purity Substances
4(3) pp476-484 .
Yoo SS, Hartnett J (1974) "Heat Transfer and Friction Factors for Purely Viscous
Non-Newtonian Fluids in Turbulent Pipe Flow" Proceedin&s of the 5th Intl Heat
Transfer Con&!", 3-7 Sept., v2 pp218-222 Japanese Sac of Mech Eng, Tokyo,
Japan
Yung B P K, Merry H, Bott T R (1989) "The Role of Turbulent Bursts in Particle
Re-Entrainment in Aqueous Systems" Chem Eng Sci 44(4) pp873-882
ZawickiI,MalcheskyPS, SmithJW, HaraskiH, AsanumaY, NoseY (1981) "Axial
Changes of Blood and Plasma Flow, Pressure, and Cellular Deposition in Capillary
Plasma Filters" Artificial Organs 5(1981) pp241-247
Zsigmondy R, Bachmann W (1918) "Ueber neue Filter" Z Anorg Allgem Chem
103 pp1l9-l28
Zydney A L, Colton C K (1984) "A Red Cell Deformation Model for Hemolysis in
Crossflow Memebrane Plasmapheresis" Chem Eng Commun 30 pp191-207
Zuk J S, Rucka M (1988) "Resistance of a Gel Layer during Ultrafiltration of Casein
Solution" Chem Eng Commun 54 pp85-92
Appendix 1 Photographs of microfiltration membranes 1
percentage
I~: •
:~"::'~'
(e) By Thennal inversion (0 By track-etch
..1.,~', I $-a~"
.'• 1:_,
,f
4_
•
I,
if "I,. ••
,""~,,
,.,~'
. J ' ..~I
-I,. ~
., "
t . ':.. (, '
~ L.: I
,
,....
,'.' • .. ,:.,,e .. ,
'l····-....' . "
, ~' .. , ' \ . " 0",£ _~, 4~'~
I ' ", 4.; • . , "r-.' 1\ •. ,Co ~ ....,~.
'.
(a) Steel
(b) Silver
(d) Zirconia/lnconel
(c) Aluminium
Appendix 2 1
Sh = O.OI05(e/d,)'·" ReSc'·'
rough pipes Kawase & Ulbrecht (1982)
rough pipes
high Se number
(a"a3 , a. constants, ug central line velocity, u+ dimensionless velocity)
- - - - - ---- -- - - -
Appendix 2 4
Grober et al (1961)
high Sc number
high Sc number
I !. ~ (4-11)
Table A
PTFE and ceramic filter with tap water
and cleaned by air backflushing and nitric acid washing
Table B
Fariey Metal Tubular Filter (No 97)
TableC
Farley Metal Tubular Filter (No 98)
Table D
Fariey Metal Tubular Filter (No 99)
LJG!:J1
(Vrnin)
4
LW
(Bar)
om
Initial
1.549
Jv (rn3/rn2.hr)
Before
1.58
After
C (rng/!)
Solids Lipids
Table E
Fariey Metal Tubular Filter (No 98)
Table F
Enka capillary filter
(at 12 Vrnin and 0.5 Bar)
Time J, (m3/m2.hr)
Clean Silica (mg/l) Silica (2 mg/l)+Lipid (mg/l)
mins Water 0.5 1 2 5 10 20
0 1.008 0.888 0.864 0.835 0.763 0.72 0.72
2 1.037 0.821 0.821 0.806 0.706 0.706 0.706
4 0.994 0.806 0.806 0.792 0.662 0.706 0.648
6 0.95 0.763 0.763 0.792 0.662 0.634 0.634
8 0.936 0.763 0.749 0.763 0.662 0.648 0.634
10 0.922 0.763 0.72 0.749 0.662 0.648 0.619
12 0.095 0.72 0.705 0.72 0.662 0.619 0.576
14 0.907 0.706 0.691 0.72 0.662 0.634 0.648
16 0.936 0.835 0.806 0.806 0.72 0.706 0.634
18 0.893 0.749 0.792 0.792 0.662 0.648 0.698
20 0.922 0.806 0.821 0.821 0.677 0.706 0.634
22 0.893 0.749 0.792 0.763 0.648 0.662 0.698
24 0.907 0.778 0.849 0.806 0.706 0.706 0.677
26 0.864 0.778 0.749 0.763 0.648 0.648 0.634
28 0.893 0.821 0.864 0.835 0.72 0.706 0.677
30 0.864 0.778 0.806 0.749 0.691 0.662 0.59
Appendix 3 Tables in Chapter 3 7
TableG
Ceramic Monolithic Filter
TableG
Ceramic Monolithic Filter
NOTES
The operating conditions, the permeate cumulative volume and flux rate with
process time of all tests in Chapetr 4 are listed in Appendix 4.
Membrane C was used to test different material, and hence its results were
not included.
The pore size of membranes J, L and M were 0.2 ~m, and that of membrane
D was 3 ~m. These membranes were only used in clean water test for membrane
selection.
Membranes K and A were tested with No 6 latex, and B, E and F with No 11
latex. However, due to the lack of the knowledge of pressure distribution, their results
were not consistent, and hence there were no further analysis on these tests. The code
of the run with * on the both sides indicate permeate pressure was greater than outlet
pressure in that run.
The results of the pressure distribution tests, membrane resistance tests, and
permeate flux rate or cumulative volume against processing time based on several
filtration models (Cake filtration, Complete blocking, Intermediate blocking and
Standard blocking) of membranes G, H and I are shown in the diagrams.
Appendix 4 Files in Table 14 2
Time Rate Cumu Time Rate Cumu Time Rate Cumu Time Rate Cumu
(min) Vmin 1 (min) Vmin 1 (min) Vmin 1 (min) Vmin 1
0 0 0 0 0 0 0 0.6149 0
2 0.2500 0.549 2 0.3361 0.672 2 0.4098 0.820 2 0.6281 1.230
4 0.1888 0.926 4 0.3434 1.359 4 0.5313 1.882 4 0.6845 2.486
6 0.1603 1.247 6 0.3282 2.015 6 0.4666 2.815 6 0.5950 3.855
8 0.1440 1.535 8 0.3296 2.675 8 0.4562 3.728 8 0.6254 5.045
10 0.1374 1.810 10 0.2882 3.251 10 0.4477 4.623 10 0.5563 6.296
12 0.1335 2.077 12 0.2824 3.816 12 0.4382 5.500 12 0.5704 7.408
14 0.1283 2.333 14 0.2732 4.362 14 0.4330 6.366 14 0.5349 8.549
16 0.1258 2.585 16 0.2804 4.923 16 0.4695 7.3OS 16 0.5287 9.619
18 0.1252 2.835 18 0.2596 5.442 18 0.4263 8.157 18 0.5183 10.677
20 0.1160 3.067 20 0.2651 5.973 20 0.3943 8.946 20 0.5220 11.713
22 0.1967 3.460 22 0.2597 6.492 22 0.4814 9.909 22 0.4837 12.757
24 0.1102 3.681 24 0.2676 7.027 24 0.4254 10.760 24 0.5507 13.725
26 0.1247 3.930 26 0.2655 7.558 26 0.4188 11.597 26 0.5245 14.826
28 0.1052 4.141 28 0.2491 8.056 28 0.4295 12.456 28 0.4902 15.875
30 0.1153 4.371 30 0.2536 8.564 30 0.4156 13.288 30 0.4406 16.855
40 0.0982 5.353 40 0.2264 10.828 40 0.4162 17.450 40 0.4497 21.261
50 0.0987 6.340 50 0.2167 12.994 50 0.4124 21.574 50 0.5562 25.758
60 0.0967 7.308 60 0.2140 15.134 60 0.2668 24.242 60 0.4497 31.319
Time Rate Cumu Time Rate Cumu Tune Rate Cumu Time Rate Cmnu
(min) lJmjn 1 (min) Vmin 1 (min) Vmin 1 (min) Vmin 1
0 0 0 0 0 0 0
2 0.90 1.8 2 0.73 1.5 2 1.27 2.5 2 1.04 2.1
4 0.79 3.5 4 0.67 2.9 4 1.22 4.8 4 0.98 4.0
6 0.76 5.0 6 0.66 4.2 6 1.01 6.9 6 0.86 5.6
8 0.72 6.4 8 0.65 5.5 8 0.89 8.8 8 0.67 7.1
10 0.63 7.7 10 0.62 6.7 10 O.SS 10.5 10 0.65 8.5
12 0.59 8.8 12 0.61 7.8 12 0.84 12.2 12 0.67 9.6
14 0.51 9.9 14 0.51 8.9 14 0.82 13.8 14 0.52 10.8
16 0.47 10.9 16 0.43 9.8 16 o.n 15.3 16 0.48 11.8
18 0.47 11.8 18 0.4 10.6 18 0.65 16.7 18 0.46 12.7
20 0.47 12.7 20 0.34 11.3 20 0.62 17.9 20 0.46 13.6
22 0.47 13.6 22 0.31 11.9 22 0.61 19.2 22 0.46 14.5
24 0.42 14.5 24 0.33 12.5 24 0.63 20.3 24 0.44 15.4
26 0.39 15.3 26 0.25 13.1 26 O.SO 21.5 26 0.46 16.2
28 0.37 16.0 28 0.27 13.6 28 0.63 22.5 28 0.36 17.1
30 0.36 16.7 30 0.27 14.2 30 O.SO 23.5 30 0.38 17.8
Appendix 4 Files in Table 14 8
Time Rate Camu Time Rate Camu Tune Rate Cumu Time Rate Cmnu
(min) Vmin 1 (min) Vrnin 1 (min) Vmin 1 (min) Vmin 1
0 0 0 0 0 0 0
2 0.81 1.6 2 0.56 1.1 2 0.56 1.1 2 0.35 0.7
4 0.74 3.1 4 0.49 2.1 4 0.50 2.1 4 0.32 1.4
6 0.68 4.5 6 0.44 3.0 6 0.47 3.1 6 0.31 1.9
8 0.65 5.7 8 0.34 3.7 8 0.45 3.9 8 0.24 2.5
10 0.50 6.8 10 0.32 4.3 10 0.39 4.7 10 0.24 3.0
12 0.44 7.7 12 0.28 4.9 12 0.26 5.3 12 0.24 3.4
14 0.43 8.6 14 0.24 5.4 14 0.30 5.9 14 0.22 3.9
16 0.40 9.4 16 0.24 5.9 16 0.29 6.5 16 0.21 4.3
18 0.37 10.1 18 0.23 6.4 18 0.25 7.0 18 0.19 4.7
20 0.36 10.8 20 0.23 6.8 20 0.27 7.5 20 0.19 5.0
22 0.34 11.5 22 0.23 7.3 22 0.26 8.0 22 0.12 5.3
24 0.30 12.1 24 0.22 7.7 24 0.22 8.5 24 0.16 5.6
26 0.27 12.7 26 0.20 8.1 26 0.20 8.9 26 0.14 5.9
28 0.27 13.2 28 0.18 8.5 28 0.19 9.3 28 0.13 6.1
30 0.27 13.7 30 0.17 8.8 30 0.17 9.6 30 0.13 6.4
32 0.26 14.3 32 0.17 9.2 32 0.17 10.0 32 0.13 6.7
34 0.26 14.8 34 0.17 9.5 34 0.17 10.3 34 0.13 6.9
36 0.24 15.3 36 0.17 9.9 36 0.21 10.7 36 0.13 7.2
38 0.23 15.7 38 0.17 10.2 38 0.18 11.1 38 0.\3 7.4
40 0.23 16.2 40 0.16 10.5 40 0.18 11.4 40 0.\3 7.7
42 0.15 10.8
44 0.15 11.1
46 0.14 11.4
48 0.14 11.7
50 0.14 11.9
Appendix 4 Files in Table 14 9
Tune Rate Cornu Time Rate Cornu Time Rate Cornu Time Rate Cornu
(min) lhnin 1 (min) lhnin 1 (min) lhnin 1 (miD) lhnin 1
0. 0..0. 0. 0. 0. 0. 0. 0.
2 2.08 4.2 2 1.78 3.6 2 1.46 2.9 2 1.10. 2.2
4 1.96 8.1 4 1.66 6.9 4 1.33 S.6 4 0..99 4.3
6 1.90 11.9 6 I.S2 9.9 6 1.24 8.1 6 o..9S 6.0.
8 1.83 1S.S 8 1.42 12.8 8 1.12 10.4 8 0..79 7.7
10 1.78 19.1 10 1.33 1S.S 10 1.06 12.S 10 0..74 9.2
12 1.70. 22.S 12 1.32 18.1 12 1.02 14.S 12 0..66 10..6
14 o..9S 16.5 14 0..64 11.8
16 0..92 18.3 16 0..61 13.1
18 o..S9 14.2
20 o..S3 1S.3
Test H3 H4 H5 H6
Flow rate 1.17 1.17 1.93 3.08 I!ntin
Rc 6547 6547 10859 17304
PI 0.90 0.90 1.38 1.86 Bar
P2 0.76 0.76 1.03 1.03 Bar
~
0.14 0.14 0.14 0.14 Bar
0.65 0.61 0.91 0.95 Bar
Temp 25 26 29 29 C
Cooc 0.2 0.120 0.12 0.12 mg/1 (No 11)
Tunc Ra.. Cornu Time Ra.. Cornu Time RaIO Cornu Time Ra.. Cornu
(min) l/min I (min) l/min I (ntin) I/ntin I (min) I/ntin I
0 0 0 0 0 0 0 0 0
2 0.401 0.80 2 0.372 0.74 2 0.422 0.84 2 0.437 0.87
4 0.534 1.78 4 0.378 1.48 4 0.417 1.68 4 0.362 1.64
6 0.582 2.78 6 0.365 2.21 6 0.411 2.56 6 0.327 2.32
8 0.459 3.75 8 0.355 2.92 8 0.467 3.35 8 0.320 2.94
10 0.397 4.61 10 0.342 3.62 10 0.384 4.20 10 0.298 3.56
12 0.399 5.39 12 0.345 4.28 12 0.381 4.98 12 0.295 4.14
14 0.385 6.16 14 0.319 4.95 14 0.390 5.74 14 0.288 4.72
16 0.365 6.94 16 0.324 5.56 16 0.385 6.51 16 0.282 5.29
18 0.403 7.66 18 0.295 6.20 18 0.376 7.27 18 0.286 5.84
20 0.354 8.43 20 0.309 6.81 20 0.378 8.00 20 0.20/ 6.40
22 0.361 9.13 22 0.316 7.39 22 0.357 8.73 22 0.279 6.92
24 0.349 9.85 24 0.276 8.01 24 0.354 9.47 24 0.250 7.47
26 0.356 10.53 26 0.305 8.57 26 0.3n 10.18 26 0.20/ 7.98
28 0.332 11.23 28 0.289 9.20 28 0.358 10.91 28 0.20/ 8.49
30 0.349 11.95 30 0.325 9.76 30 0.352 11.62 30 0.247 8.99
32 0.385 12.63 32 0.267 10.37 32 0.356 12.30 32 0.231 9.42
34 0.339 13.36 34 0.285 10.88 34 0.327 12.98 34 o.ln 9.89
36 0.346 14.04 36 0.246 11.43 36 0.330 13.64 36 0.242 10.37
38 0.333 14.71 38 0.270 11.97 38 0.333 14.29 38 0.304 10.82
40 0.324 15.36 40 0.291 12.50 40 0.321 14.95 40 0.211 11.36
42 0.319 15.99 42 0.263 13.07 42 0.323 15.60 42 0.236 11.80
44 0.308 16.62 44 0.280 13.53 44 0.332 16.24 44 0.228 12.25
46 0.315 17.25 46 0.196 14.06 46 0.314 . 16.88 46 0.212 12.70
48 0.317 17.89 48 0.243 14.50 48 0.310 17.51 48 0.224 13.11
50 0.324 18.51 50 0.245 14.97 50 0.316 18.12 50 0.204 13.55
52 0.305 19.13 52 0.231 15.46 52 0.303 18.74 52 0.214 13.96
54 0.302 19.74 54 0.247 15.89 54 0.302 19.35 54 0.210 14.38
56 0.304 20.35 56 0.194 16.36 56 0.308 19.94 56 0.204 14.79
58 0.307 20.97 58 0.225 16.n 58 0.293 20.54 58 0.203 15.22
60 0.321 21.54 60 0.221 17.21 60 0.293 21.11 60 0.222 15.61
70 0.261 24.46 70 0.210 19.37 70 0.2n 23.92 70 0.191 17.61
80 0.263 26.91 80 0.212 21.38 80 0.268 26.59 80 o.ln 19.44
90 0.229 29.39 ·90 0.191 23.32 90 0.258 29.16 90 o.ln 21.18
lOO 0.233 31.61 lOO o.ln 25.14 lOO 0.246 31.63 lOO 0.170 22.87
110 0.214 33.78 110 0.174 26.86 110 0.237 33.95 110 0.163 24.50
120 0.201 35.91 120 0.167 28.53 120 0.217 36.42 120 0.156 26.05
122 0.212 36.31 122 0.160 28.85 122 0.258 36.86 122 0.148 26.35
124 0.206 36.73 124 0.157 29.16 124 0.219 37.33 124 0.144 26.65
126 0.199 37.13 126 0.150 29.47 126 0.210 37.75 126 0.145 26.93
128 0.195 37.52 128 0.153 29.n 128 0.209 38.18 128 0.144 27.22
130 0.194 37.91 130 0.150 30.07 130 0.214 38.61 130 0.142 27.50
Appendix 4 Files in Table 14 11
Membrane J, L, M. O.2um
Test J\ 12 13
Mode Batch Batch Batch
Aowrate 2 2 2
Re 11214 11214 11214
PI 0.69 1.38 2.00
P2 0.14 0.83 1.52
.pp 0.00 0.00 0.21
Pt 0.41 1.1 1.59
P(BiF) 3.12 3.12 3.12
Temp 20 20 2S
Cooc water water water
Time Rate Cumu B/F Tune Rate Cumu B/F Tune Rate Cumu B/F
(mm) Vm"2.hr 1 .ec (mm) l/m A 2.hr 1 sec (mm) Um"2.hrl .ec
0 2880 0 0 2720 0 0 3936 0
10 2400 36 10 2016 33 10 2912 48
20 1920 66 20 1728 60 20 2400 86
30 1600 91 30 1568 84 30 2240 119
40 1440 113 40 1440 106 40 2016 149
SO 1280 131 SO 1312 126 SO 1760 178
60 960 147 60 1216 144 60 1760 203
70 880 160 70 1184 162 70 1632 228
80 800 173 80 1120 179 80 1568 251
90 800 184 90 1120 195 90 1440 274
100 720 194 100 1040 211 100 1440 295
110 560 203 110 960 226 110 1440 316
120 480 210 120 928 240 120 1280 336
130 384 217 130 960 2S4 130 1216 354
140 352 222 140 880 267 140 1120 371
ISO 304 227 ISO 848 280 ISO 1120 388
152 304 228 152 832 282 152 1120 391 3
154 304 229 154 832 285 154 1120 395 3
156 304 230 156 832 287 156 1120 398 3
158 304 230 158 832 290 158 1056 401 3
160 304 231 160 864 293 160 1120 401 3
162 304 232 1 162 1152 296 3
164 304 233 1 172 1380 312
166 312 234 2 182 996 330
168 312 235 3 192 996 345
170 320 236 3 202 948 359
112 320 236 3 206 892 359 3
Appendix 4 Files in Table 14 13
Test L "M"
Mode Single Single
Aowrate 3.6 1.37 IJmjn
R. 20200 7689
PI 2.(11 0.17 BB<
P2 0.83 0.00 Bar
Pp 0.00 0.00 Bar
Pt 1.45 0.09 Bar
P(BIF) 3.72 11/ Bar
Temp 20 25 C
Cooe water 0.012 mgll (No 6)
Time Rale annu B/F Tune Rate Curnu Time Rate Cumu
(min) Jlmll.2.hr 1 sec (min) l/m A 2.hr 1 (min) UmJl,2.hrl
0 2100 0.0 0 0 72 38 6.7849
90 480 17.4 2 100 0.234 74 35 6.898
120 270 19.1 4 118 0.5428 76 34 7.0021
180 150 21.0 6 94 0.8962 78 33 7.1043
191 150 21.2 2 8 93 1.1791 80 32 7.2039
193 150 21.3 3 10 90 1.4581 82 35 7.3
195 450 21.4 4 12 63 1.7286 84 32 7.4049
197 450 21.5 5 14 109 1.9169 86 35 7.5005
199 450 21.6 4 16 42 2.2429 88 30 7.6065
201 450 21.8 4 18 121 2.3697 90 30 7.6961
203 450 21.8 4 20 76 2.7315 92 30 7.7848
22 77 2.9604 94 29 7.8749
24 71 3.1923 96 29 7.961
26 67 3.4042 98 29 8.049
28 70 3.6061 100 28 8.1347
30 60 3.817 102 28 8.2181
32 57 3.9983 104 29 8.3013
34 59 4.17 106 24 8.3873
36 55 4.3483 108 28 8.4591
38 46 4.5142 110 27 8.5435
40 56 4.6523 112 27 8.6257
42 53 4.8205 114 26 8.706
44 53 4.979 116 26 8.7854
46 59 5.1374 118 27 8.8629
48 48 5.3142 120 25 8.9427
50 47 5.4581 122 23 9.019
52 45 5.6002 132 23 9.3622
54 45 5.7365 142 16 9.7061
56 35 5.8725 152 32 9.9422
58 41 5.9769 162 25 10.4192
60 38 6.1008 172 24 10.8013
62 38 6.2158 182 22 11.1608
64 38 6.3309 202 21 11.8257
66 41 6.4439 222 20 12.4563
68 37 6.5662 242 19 13.0509
70 36 6.6764 272 17 13.8937
302 16 14.6692
332 16 15.4101
Appendix 4 Files in Table 14 14
0.8
0.6
0.4
0.2
oL-~~~~--~r=~~==~----L-------~--------~
o 5 10 15 20 25
Flow rate (1/min)
P1 P2 P3"
o ---6--- .... ·0·....
Test 01
Jv (Vmin) Membrane G
12 r-------------------------~--------------~~--~
,/' .........
11 -. ----.- ------- -------. ---_ .. -.. ---....... -.............. -._._-._.". .. -._._._ ....... --._ .... -._--._.-._. - ~:- ... _.. --_ .... _.... -
10 ·y·p~ess~~e·disi-;ib~ii~-~·i~st····-·"lj/:'~·A..t:I.......... .....:.-:d::~::::::-Q.-...[;L....---..
: :::::::::::::::::::::::::::::::::::::::..: . :.-?~::::::::::::::
£::.. 0 /
...:.::::~~:.'::::::::::::::::::::::::::::::::::::::::::::::
/" .
7 ._._. __ ._._._ .... ______ .. _____ ... _______,t____________ ._.-
, .
.. : ....::---------.----.---------------.----------------------.---------
,, ...,-
: :::::::::::::::::::::::::::~~to.:;;.~;:::·:::;'~::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
" 0'-
4 ..... -............ -.,., .-.. :: .... --..... -..... -.-.... --..... --..... -....... -.... -.-........... -............ -.-.... -.-.... -.. .
: ~:;>:2~::::·:~~:::·:::~~=:~·~~~~~~~!.:~~~::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
o&-__-L__ ~ ____L __ _-L__~L-__~__-L____L -__~__~
o 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9
Pt (Bar)
by average by P1 by P2
o --'-A--- .. -··0 .....
Test 01
Appendix 4 Files in Table 14 16
0.004 f-.............................................................................................................................
0.00 1 f-.............................................................................................................................
OL-_ _ ~ __ ~I _ _ _~_ _~_ _ _L_I_ __ L_ _~
W (m 3 ) Permeate volume
0.08 , - - - - - - - - - - - - - - - - - - - - - - - - ,
0.072 ............................................................................................................................ .
0.064 . ..... .............. ................... ... ..... ................. ..................... ................ . ................... .
0.056 . ..... ............ ..... ... .............. ...... .............. ...... ................. ..... . ................................. .
0.048 . ................ ...... ... .............. ...... .............. ...... ........ ............................................. .
0.04 ............... _.. -.... __ . _." -.. -.-.... ------ --.. ----". --.- ...... --- -_.......... -.----... -- -.- --... _-----.---............
0.024
0.01 6 .................. ... . .................................................................................................... .
O~-----J---------L----------~--------~
o 240 460 720 960
t(s)
G1
o
Test 01
Appendix 4 Files in Table 14 17
12,800
12,600
12,400
12,200
12,000
11,600
11,400 ...........................0'............................................................................................
11,200
11,000 L-_--.JL-_---1_ _---1_ _---L_ _---1._ _.....l.._ _.....l.._ _...J
o 120 240 360 480 600 720 840 960
t(5)
o
Test 01
12,600
12,400
12,200
12,000
11,600
11,200
11,000 L-_-'-_---L_ _-'--_-'-_---'_ _-'--_-'-_---'_ _-'-_....J
o 0.01 0.02 0.03 0.04 0.05 0.06 0.07 0.08 0.09 0.1
W (m 3)
o
Test 01
Appendix 4 Files in Table 14 18
O. 15
o
--- -- -..... ----.. __ -_-- --- -- ---- _. -----. ----.- --- -- --_ .. -' .. ". -... ---_...... _---
0.05 -.-----------_ ..... -._----------_.-.-.-.----._---_ .. ---------.. ---.-----... ---.-_.------.. _.----._ .. -----_.-.---.. _-.--------
o
Test Gl
14
12
10 .................................... .. ..................... 0' .............................................................. ..
8 ............ .61.. ........................................................................................................... .
6 . .. ........................................................................................................................... .
4 ................................................................................................................................. .
2 ................................................................................................................................. .
oL-_ _ L-_~~_~L-_~L-_~ __ ~ __ ~ __ ~
o
Test Gl
Appendix 4 Files in Table 14 19
o.oos
0.004
0.003
6 0
0.002 -------4
--- _. -_... -
.-.-~-- -------- ._- - -
l!.---l!.--__
_. --------... --- ... _-- ----._.- --- ...--------_ .. -- .. -. ------.......-..... __ ... _-_. _.. -
"
...~.""'~:Q::::3i ....
6
... =----l),.---&---I::J....--{;}-__ _
0.001 ................................~~::I!l::, .........................~~----~.........................
.... ..,,-o""-G''''-0'''';;':-':-fi--n --
~~-,*- "'" "".;1£:"'"
0.012
~ ..e-' ~'"""
._--.. ----_..... ···----------··---···"..·---·····--·····------···o."J··-----::;;.~-.--- .. -.-----... -.---..... -.-.--.
);J ..0"'··~-~
0.01 ........... ··············If·················:·-e-·'~················ ..........................................
/' _.J;~':'X'"
0.008 ........ ···········~~(···········(y·x························· ....................................................
" ......X"
0.006 ... ·····W·········,j}/.....····...... ···· ....····· .. ··.. ·········..·· ...........................................
, .0·~
0.004 .- ····_,!···--r:;,x---------------------------------------··-------..... --... ----------.------.... ------.... -..... ------
IZI' ....)t-'
O.O~ ,;j~ .....--.-.------... -.---.-.-.-.-.-.-.............................................. _-_ ................ _...........
O~----~--~~----~----~----~----~----~--~
o 240 480 720 960 1,200 1,440 1,680 1,920
t(s)
G2Il G2Il G213 G2I4
0 ---8--' ·····0····· -"*"-
TestG2
Appendix 4 Files in Table 14 20
~~~~~~~;~§~;~~;::~
100,000
90,000
80,000
70,000
••.• ' J -A---t".-
60,000 ................................................::t!r--k~:...............................
~ __ A--
50,000
40,000
..
.:~~:~~~:~~ ~~~::::::::::::::::.uuu.u.uu . . .u
30,000
20,000 f-;43-."'
.. t;J•••••••••••.••••••••••••••••••••••••.•••••••••••••••••••••••••••••.••••••••••••••.•••••••••••••••••.••••••
10,000
O~-~~-~--~--~--~---L--~--~
o 240 480 720 960 1,200 1,440 1,680 1,920
t(5)
G2I1 G212 G213 G2I4
0 --~--. ·····0····· -""*""-
Test 02
-- ---
1~,000r----------------------~
:~:~ ~:~~jl~~~~~~~S~~~~;t
70 000 "":::-:.-:......::.O-.,,:Q:::::~.................................................................................. .
, .. 0-.... -er:---tJ.---
:':~ =::'::::::::::::::::::::::::::::::::::::::::~~.uu~:~:~:~~~~::~:==~~~~~~~ . .: : : : : : : :
I _ _ _ _ _ _ ~-----
Test 02
Appendix 4 Files in Table 14 21
1.6 .--_.. __ A. - - - - - • • ___ A. - - - _ • • • __ A. - - --_ •• --_ •• - - - - . . -_.- _. --- _. ---- - ---- _. - - - _ • • • __ A. - ---------- - - - - - ____ AA. - - - - - • • - - - - . - - - - . _ .
1 .4 --- _.- ---------------.. ---.... _•. ____ AA • • - __ • - - _A. - - _ . - ___ A. - - - - - - - - - - • • • - - _ . - - __ A. - - - - ___ • • - _ . - --- ------- ----- -- --- •• - •••• _.
---'--
1 .2 --- _.- __ A. - ____ A - .-_. -- --- ••• --_. ----- - --_. ---- _ • • - - - • • - - - - - ____ A. - --_. -- --- -_. --- -- ---._. ---- - - -_- _._---. ----'" -::;..:...-"!".":'
..----.;'"
1 --------------------------------- ---------------------------------------------===~~~-:~'~-~.:::4_;::::.-.·.
0.8 ..... -.----.-.. ------..... - -----------------------------------------;>-.-"------~:;;.)}..""-.0:::::\:,. ..'''0------
o /), /), _-~-- /), ~__ --._..__ 0---"
0.6 --------------------- --------------~·~-~~:::;::";--~;.~-::-O:::""O--------------------------------------
~::~:~i;;~~:;-9:-:~~~::::::;:~~:~~~
1,200
800
p._.~ A __ -
-.--.;....~ -A---~---
....... _./!r--
400 ~"-ti_=.:::4.==--.~--~-~- ------------------------.----------------.-----------------------------------------------
0.00072
~ 0 o····... ~ IS. l:s.'A.t;:.
."-=~ ...............O··e::(J-6-::··::·:::4"1£!;£.............
"-*-~-_ Cl 0···.... ""
0.00048 ...................... KK)"(~·~·~:O::0-Q.·.-O:.Q~D.:i5::::.::~·:···....... ........
0.00024 ..........................................................~~1~.~ ..~~".;(:}j;;*·¥:ffi::~;;;;"
o L-_ _L-_ _ _ _- L_ _- L_ _ _ _ _ ~ ~ L-_~
240 000
,
f------------------------------------------------------_________________________________________
~
**11[_ _ _ _ _ _ _
~~
~
21 0,000 f--------------------------------------------------------------------~¥>£------------------------------------
~~~
180,000 ------------------------------------;z.~~~~---------------------------------------------:::::::::::::::-:-
150,000 ------------------------~~-------------------------------------------------:0-6:::::::::-----------------
_~~ 1d·1d·(if·e- _-----
120,000 ::::::---*~~-:><:
.. -......... -----..-... -----..
~. 'Q::~:,e-""'-
"'.Id·
-----.-.-..---. -~:::::;;'_'~-~.._-----
------....... --. -.....
~ o·_o·· tr---
90 000 __________________ "e-,e::~:·_.-___ .__ .::I!.~&-A::l[-"'!!:~.- ..... ----....... -.--.--..
, .f:J·0 -A-A
.. -0.-0 _e-.A-er- A
60,000 --'-~5.-tr-~/},.--""- --
-~
30,000 I I I I 'I I 11 I
o 240 480 720 960 1,2001,4401,6801,9202,1602,4002,6402,8803,120
t (5)
G3/1
o
G312
----6.--- "'--0-----
G313
-*""-
G3/4
TestG3
240,000
210,000 .
-------------------------- .. _---.------------_.---._---------_._--_._." .. "
1.8
1.6
1.4
1.2
0.8
0.6
TestG3
...- 0 .. ' --
1 ,600 - ...... ;;/2·· .. ··· .. ·0·0;~::::::······;;:.:i5.;.-,;.~-"'::::::::~~·~:.· .....................=--
...-"'- ~ g.. . _--tS' -
1,200 ~:.. ··"' .. ·.... · .. p:,P"· .. ·l5...fSo.a_t!i·6 .... ·.. · .. ·i'i·· ..· .. ·· .........................................
. [), ---
800 :-:.~1$f~~::::· I'l .. .. ....... :~..............................................................
400 """"", .................................................................................................................... .
oL-____- L____ ~IL- ____JI______ ~ _____ ~I ____- L____ ~
TestG3
Appendix 4 Files in Table 14 25
0.0007
11
0.0006 ........ "/5.............................. . .............................................................................
~~
0.0001
oL-_~ __- L_ _ ~ _ _ _ _L -_ _ ~ _ _- L_ _ ~ _ _ _ _L -_ _ ~ __ ~
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t (s)
G4/1 G412
o ---er--.
TestG4
0.016
0.014
0.012
0.Q1
=_8--0-
-8"-=
0.006 .. ·········;:;.::::a:::Ef"~~·~·····························
8-""'-'
..................... ...............:a-.a~....................................................................... .
0.004
8"-=
=_..[3-
0.002 ······=ri;;S"······.. ·································.. ··..........................................................
O~~-L __ ~ ____L -_ _ ~ _ _- L_ _ ~ ____ ~ _ _- L_ _ ~ __ ~
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t (s)
G4/1 G412
o ---{3--.
TestG4
Appendix 4 Files in Table 14 26
150,000
120,000
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t (5)
G4/1 G4/2
o ----0---
TestG4
150,000
-----
,-'........................ ---_._---_....................... _.. .__ ................. __ ...... __ .... __ ._------_.... .
120,000
90,000
8O,OOOL-~L-~-~-~-~-~-~-~-~-~-~~
o 0.001 0.002 0.003 0.004 0.005 0.006 0.007 0.008 0.009 0.01 0.011 0.012
w (rrf)
G4/1 G412
o ----0---
TestG4
Appendix 4 Files in Table 14 27
1.8 ._._----------------------------._.--------------------------------------------------------------------------------------------
1.4 ---------------. ------. -" ... -.-_ .. -.------'- _. -----------------._------------.... ---.---_.------. -.--.. ,.. ------. _. ----.. --_. --
.................................................................................g.... . ~;:'lr'"·-:-,..,···e···"'···
0.4
oL-e-~--~----L----L--~----~---L--~~--~--~
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t(s)
G4/1 G412
o ---0--'
TestG4
4,500 ._-----_._-----------.--------------------------------._---------------------------------------------------------......::::.----
..................................................................ts .........1!....."'.>4~~E:-:......................
-zr/6, '"
4,000
6. ......... ...
3,500 -----------------------------------------------------------A-----------~~:::---------
/
_________________________ ---------
~~ 0
............... 0 0
3,000 ---------------------------------------------------:;~ .... ------------------------------------------------ -------5--
/
/A~U
'" 0 0 0
2,500 -------------------------------- -~:::: 8------------------ ----------- - --- ----------------- -------------------------
t:.-~1S~ '"
2,000 .......... :;"--Ef::.............D ............. ..
1,500
--
... ... -~
.. "z,..................... . ........................................................................................... ..
1,000
500
OL-__- L_ _ ~ ____ ~ __ ~ _ _ _ _L -_ _- L_ _ ~~ __ ~ __ ~ __ ~
o 240 480 720 960 1,200 1,440 1,680 1,920 2,160 2,400
t (s)
G4/1 G412
o ---0--'
TestG4
Appendix 4 Files in Table 14 28
1.2 ---------------------------.-.-----. -_. ----_. -_. --- _... -------------------------------------- ____ A_A • • - _. _. - -- ---. - - - -- -- _. - - .
5 10 15 20 25
Flow rate (1/min)
PI P2 P3
0 ---0--. ·····0·····
Test HI
Jv (1/min) Membrane H
5,---------------------~,~__,
/
,/
4.5 ._--... --... ----....... --.---.'.--_ ....... --.. '.---------------------------------------_._-------.. -------:,',;.............. ---- .:;.
6,,,,,-,,,; CD ....•...•
3.: ::::::::::::::::::::::::::~~::.~~~~~~.~~~.t.'.~~.~.~~::~::,~~=~~~=;;~::.=:;;~::::~~~::::::::::::
3 ..................................................................... .::.......13"::.. ................................
2.5 ...................................................... ·7'~<·:..:. ,::-::::::.P.l.;;.O_5(P.1.+.P.2).,..P.P .....
""," /.,- DO
2
1.5
:::::::::::::::::::::::::::::::::=~~'!:>:::~~::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
6,./.
" ,,;;;:::i:~~:~::....::::....:
O~~~_~_L-_L-_L-_L-_L-_L-_L-~~-J_-J
o 0.1 0.2 0.3 0.4 0.5 0.6 0.7 0.8 0.9 1.1 1.2
Pt (Bar)
by average by PI by P2
o --'-6--. ... .. 0 .....
Test HI
Appendix 4 Files in Table 14 29
I I I I
0
0 200 400 600 800 1,000 1,200
t (5)
HIlI HI/2 HII3 HI/4
0 ---6--' ·····0····· -~-
Test HI
W (m 3) Permeate volume
0.025
0.02
.El ..0
,,,'" 0·········
0.Q15 ............................................. ···>;»<···:::c;r. . ,,::::::······················x.:;:··
"",,"
,,'
.......
Q( . 0····· /
....
-...--- ~-
--~ --
0.01 ............................ ·~;0'··::::.,..0········£7-~····························· ................ .
" .. - ./
"',," ... 0 ~ ........
)2l" ••.... ------
/0"
............ y<.:.~ X
.... ~............................................................................................ .
0.005
:...·::.,x
---
o~---~----~---~----~---~
o 240 480 720 960 1,200
t (5)
HIlI HI/2 HII3 HI/4
o ---8--. .. ..·0··... -~-
Test HI
Appendix 4 Files in Table 14 30
64,000 c-..........................................::.:~.,..-=~--
...............................................................
..,..-
:: :~~;;~;=:::::~:~;;;;~~:-~
32,000
6------6:----
F":::::tl::::::::············,.,········· ......... .
24,000 f-..........................................................................................................................
16,000 1-......................................................................................................................... .
8,000 1-......................................................................................................................... .
o L -__~___L-I__~I____IL-__~I__~IL-__~___'L-__~I__~
o 120 240 360 480 600 720 840 960 1,080 1,200
t (5)
H111 H1/2 H1/3 H1/4
0 ---0--. ·····0····· -"*--
Test HI
::::::: :==~~==::;::~"~~;;~~-;
// 0-.... 0-.... 0-......
. .:. .
:~:::::::~::;;;;;~~::::::::~::::::~;~~;~~~~=:: ~~~:.:.:.~~~;;~~:~~:~~~~~~:~
A-_____6------6:
32,000 _r.",,::::.................................................... . .......... .
~
24,000 _ .......................................................................................................................... .
16,000 _ ......................................................................................................................... .
8,000 _ ......................................................................................................................... .
OL-__~I____L-I__~I____
.IL-__~I__~I~__~I___IL-__~I__~
o 0.003 0.006 0.009 0.012 0.015 0.018 0.021 0.024 0.027 0.03
W (rri3)
H1/1 H1/2 H1/3 H1/4
o ---0--. um0um -"*--
Test HI
Appendix 4 Files in Table 14 31
oo~ ::::::::::::::::.~=:~;;;~:~~::~::~.~.:.::=::::::::::~~~~~~~~~~~~~:~:=:~:::::::::::::::::::::
. ···········0··· ~-----~----
o~~: ~~~~~~~~:~~~~::~~=::::::::::.:
n
. . . . . . . : : : : : : : : : : : : : : : : : : :. . . .: : : : : : : : :
o ~
I I I I I I I
o 120 240 360 480 600 720 840 960 1,080 1,200
t(S)
Hl/1 Hl/2 Hl/3 Hl/4
0 ---6.--' ·····0·····
-""*""-
Test HI
0.0015 ..........................................................................................................................
o
0.001
66
-----A.
7S-A-?:,.-n-"ts.-A_"6_
0.0005 .............................................7S:ts.7/},;~£r.......,..-A"-&~~---n: ........................
l!.
o ~--~--~---~--~--~~--~--~
o 480 960 1,440 1,920 2,400 2,880 3,360
t(S)
H2I1 H212
o ---e,--.
TestH2
O~--~--~--~--~--~--~--~-~
o 420 840 1,260 1,880 2,100 2,520 2,940 3,360
t (S)
H2I1 H2I2
o ---8--'
TestH2
- - - - -
: : : :.: : : : : : : : : : : : : : : : : : : : :.: : : .: : : : .: := ;~ ~ ~ ~: ~ ~ ~: :
210,000
200,000
190,000
/)r.l!r
:·::::::::::::::::::~i~?:~~~::::·::::::::::::::::::::::::::::.::::::::::::::::::::.::::
180,000
170,000
160,000
-IS
150,000 .....~::fS.......................................................................... ...........................
~~ I:;
140,000 ~t:I.A................................................................. ............................................
130,000
1~,OOO
110,000
100,000
90,000 0 .....................................................................................................................
80,000 L-__-'---__--'-____L-__-'---__--'-__----''--__-'---__--'-____'----'
o 360 720 1,080 1,440 1,800 2,160 2,520 2,880 3,240 3,600
t (s)
H2I1 H2I2
o ---0--.
Test H2
160,000
: ·: · ·:·: . ::····:·:~Z:=······:. :· ·:. :·: ·:· ·: : : : : : : : : : : :. :. .:.: :
..k".l!r
/[;.
140,000 ~.:;o. ...............................................................................................
120,000 ............................................... ;:; ..~~~
.......= . .. .......... ......................................... .
100,000
o
8O,OOOL----'-------'-----L----'-------'-------'L----'-------'-----L----
o 0.002 0.004 0.006 0.008 0.01 0.012 0.014 0.016 0.018 0.02
W (m3)
H2I1 H2I2
o ---0--.
TestH2
Appendix 4 Files in Table 14 34
0.9 ----------------- __ A. _. _A. -_. -__ .------------------ .--_. ------. ----------------. ------------ --.. ----.--.--. --_.------.---_ •••
~~~s
: : : : : : : : : : : : : : : : : : : : : : : : : : : :::::::::~;~~~~~~:~~~~~~~~~:t;, . . . . . .
2,400
2,100
'~dS~-~ t;,
1,800 ......................................A.A~ ........I:;.................. ..
t;,~&-ts:
900
600 .......................................................................................................................... ..
300 .......................................................................................................................... ..
oL-____ ~ ______ ~ ______- L_ _ _ _ _ _ ~ _ _ _ _ _ _L -_ _ _ _ ~
10 Jn~
0.0006 f-·················GilB-B·mmlWEll!B·················································· .................. .
U
0.0004 f-..................................................... ·······················B-··::::··:[·Gj::··:::-···::r··t:J:r··~·--QlwQ=:·1
-
0.0002 1-......................................................................................................................... .
W (m 3 ) Permeate volume
0.04 r---------------~--------.
0.036 ... -.......... ----... ---... ---.... --_.--.--.----....... ---.............. ----......... ------------.---.-.
0.032 .................................................................................... ..
0.028
0.024
0.02 .... -...... _.... --...... _A • • __ • _ •• - ._. - •• - - - - -- ---- - - - - - --- •••••• -_ •• - •• --
0.016 .................................................................................... .
0.012 ............................................................................................... .
O.OOS ..... _...... _. -_. -_--- _. ----_-..... _. -........ _. _....... -' .. _...... -.... __ .. _. --_-__ . _.. -----..... _._._-_.-
o~--L-~--L--~--L-~--~--L-~-~
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t (5)
H3
o
TestH3
Appendix 4 Files in Table 14 36
200,000
190,000
180,000
170,000
160,000 ..d:LY.
.........................................................................
150,000
140,000
130,000
120,000 ·rP····················································.............................................................
110,000 '---'---'---'-----'------'--'----'---'--'------'---'---'----'
o 600 1,200 1,8002,400 3,000 3,600 4,200 4,800 5,400 6,000 6,6007,2007,800
t (5)
H3
o
TestH3
200,000
180,000
160,000
140,000
0.9 -----.---........ --.... ---............ ----." .. -.-...... ---.. -----...... --.. -.......... -... -------............. __ .............. .
0.6
0.5
0.4
0.3
0.2
0.1
0~~~L-~~L--L__L - - L__~~__~~__~~
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t(s)
H3
o
TestH3
1,500 ._- -------_.--._ .. -------- .. -------------_ ... _._--.- .. -.--- .. __ ............-... _.......... __ .
o
1,200
900 ~ .......................................................................................................................
600 .......................................................................................................................... ..
300 ........................................................................................................................... .
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t (s)
H3
o
Test H3
Appendix 4 Files in Table 14 38
0.0002 ......................................................................................................................... .
o 840 1.680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t (s)
H4
o
TestH4
0.03 ............................................................................................................<
...""
.. ...,..
0.025
0.02
0.015 ............................................................................ ..
0.01 _.------.. ---------_._- .... _------.. --------_._---------------------... ------.. --------.. -------... --------..... -.... --
0.005 ............................................................................................................. .
230,000
220,000
210,000
200,000
190,000
180,000
170,000
160,000
150,000 '-----'-_--'-_-'-_-'---''---'-_-1-_-'-_'-----'-_--'-_--'------'
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t (s)
H4
o
TestH4
0.3 o
····················G········· ... 0' .................................................................................. .
0.2
o
................
0
··G··················································....................................................
0.1
o
... .Qj....................................................................................................................
o~~ __- L__- L__ ~ __L-~L-~__- L__~__L -__L-~__-"
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t(s)
H4
o
TestH4
1,200
800
400
600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t (5)
H4
o
TestH4
Appendix 4 Files in Table 14 41
o
0.0008 ...........................................................................................................•..............
o
0.0006 .......................... .
0.0004 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .=
... ... ...
~~~d
0.0002
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t (s)
H5
o
TestH5
0.032 ..................................................................................... .
0.028
0.024
0.02
0.016
0.012
0.008
0.004
O~ __ ~ _ _ _L -_ _- L_ _ ~ ___ ~ __ ~ __ ~
200,000
190,000
180,000
170,000
160,000
150,000
140,000
130,000 L-----'-_-L_-'-_-'-------''----'-_--'-_-'-_'----'_--'-_--'---'
o 600 1,2001,8002,4003,0003,6004,2004,8005,4006,0006,6007,2007,800
t (5)
H5
o
TestH5
210,000
200,000
190,000
180,000
150,000
140,000
130,000
120,000 L-_...I.-_-L_-----''--_..L._-L_---'_ _-'--_--L_---'.l_---'
o 0.004 0.008 0.012 0.016 0.02 0.024 0.028 0.032 0.036 0.04
W (m3 )
H5
o
TestH5
Appendix 4 Files in Table 14 43
0.9 ---... -------_ ..... _.... _.--.. _-------_.-...... _--------.. -............................. --------------... -.... _-_ ...... _...... .
0.8 ----........ --.. --...... --....... ------... -......... -............... --.... ----... ---.. -----.----.--.--....... -----...... -----..
0.4
0.3 FDY"t:l···················································.................... .
0.2 ..................itj.... ..............................................................................................
0.1 ... 0 ......................................................................................................
o~~ __ ~ __- L_ _ ~ _ _L -_ _L-~__- L_ _~_ _~_ _L-~__~
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t(S)
HS
o
TestH4
2,400
1,800
1,500
900 ........................................................................................................................... .
600 ........................................................................................................................... .
300 ........................................................................................................................... .
OL-~ __ ~ __- L_ _ ~ __ ~ __ ~ __ L-~ __ ~ _ _- L_ _ ~ __ ~~
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,600 7,200 7,800
t (s)
HS
o
TestH5
Appendix 4 Files in Table 14 44
0.0008 ........................................................................................................................ .
o
0.0006 ~·~...;g··:b····..,.:,··:···············O······················· ................................................................. .
0.0004 .................................................................... .
o
0.0002 ......................................................................................................................... .
OL--~-~--~-~-~--~-~--~-~-~
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t(S)
H6
o
TestH6
0.024
0.021
0.018 .......................................................... .
0.015 ..................................................................... ..
0.012 .................................................................................. .
0.009 ..... -.. _-_ .... ------_ ............ _..... __ ...... _._ ..... --_-._ ... _.- -----.... -_. --........ -.-.. -
0.006 _. _. _.. _.-... _.. -----_ ..... -_ ........... _._._ ... _........ --.. -...... ---_."'---__ A - •••• _. - ••••••••••••• --.-
0.003 ....... --................ -----------.-.-----...... ------.... _.. -.......... -.--.. _-_ ......................... -.... _.-
O~ _ _- L_ _ ~ _ _ _L -_ _ ~ _ _- L_ _ ~ __ ~
280,000 .........................................................................................................".·.....-rW-"'f
280,000
240,000
200,000
180,000
180,000
o
140,000
280,000
260,000
240,000
220,000
200,000
180,000
180,000
o
140,000
120,000 L -__-L.__---1.____L -__- ' -__--'-__- - " ' - -__- ' -__--'-__--"'------"
o 0.003 0.006 0.009 0.012 0.015 0.018 0.021 0.024 0.027 0.03
W (m3)
H6
o
TestH6
Appendix 4 Files in Table 14 46
- In(J/Jo)
1.2 Complete
...-_ _ _ _ _ _ Blocking
_- L ._ _ _ Model
_ _-"'-_ _ _ _ _ _ _ _ _- - ,
1.1 .. ....-;::l;UW
... -----.................................................................................. --...... --.-.... -----.-"'
1 o
.................................................................................................... ···D·················
0.9 ······························8······················· .................... g..... . .....................................
0.8 .............................................. [j~ ......... l:J .......................................................
0.7 ................................... J:l ... Cl..... D·····················································...............
0.6 .................... 0 ... o... ... ...................................................................................... .
0
0.5
---"::D....... __ ... __ .... __ ... ___ ... ___ . __ ..... __ . ___ .•....•.•. __ .... ___ ..... __ ....... ___ ......•.... _____ .•... __ ....•. _.. .
0.4
o
0.3 .-cP.-------....---.... -----........-...-----.....-----... ------.-------... --------.-.-.--..... ---.-........................
0.2 El····················································· ........................................ --------.. ---... ----.--....... .
O. 1 ••••• _•• _•••••• _.•••• _.• -_ ••• "._ .••••• _.•••••••• -••.• -•. _.•••• -_ •••.••••••••••••.• -••••••• ---_ •• _••••• _. _.- --_ ••••.• ---.• -••. _-
O~~_~_~_~_~_~_~_~_L-_L-_L-~_-J
o 600 1,200 1,800 2,400 3,000 3,600 4,200 4,800 5,400 6,000 6,800 7,200 7,800
t(5)
H6
o
TestH6
1,600
o
0 -.........._...... -----..... ---... -.-----.... _. _.. _. -.-----..----......---.. _._ ..-... ------. --_.... --_. -........_. -----
1,200
800
400
600 1,200 1,800 2,400 3,000 3,800 4,200 4,800 5,400 6,000 6,800 7,200 7,800
t(5)
H6
o
TestH6
Appendix 4 Files in Table 14 47
0.8 -- ---- -- -- ---- ----- ---.-.------- ----- ----------.--------.--.- _.. "---- -- -- - .. -.-- ---" .. _.. -. -- -.. ---_ .. --_. -- _. -_. _. ---- -- --_. --
5 10 15 20 25
Flow rate (1/min)
Pl P2 P3
o ---i!I-_. ..... e .....
Test 11
Jv (Vmin) Membrane I
5 r - - - - - - - - - - - - - - -__-~~,n-------~
4.5 .......................................................................
.. , ...
12').-;;
·········.~r············································
...-;.~-;...
3.: :~~:~;~~~:;~:~;~~;;~~:~i:~~:~~~~::::··::::;;;;>~S:::::::::::::::::::::::::::::::::::::::::::::::::
3 .............................................. ,.~
.......................................................................
/ O.5(P1 +P2)-Pp .
..~/
2.5 ........................................
..yf.1S.
, ............................................................................. .
2
.. -;-;....
............................... g~.........................................................................................
OSL~~
....:," ____ ~ __- L_ _ _ _L -_ _- L_ _ _ _L -_ _- L_ _ _ _L -_ _- L_ _ ~
Test 11
Appendix 4 Files in Table 14 48
0.0018 ·················································OD"it·'bOCtri~D~···~··::;··········································
0.0015 ................................................................................. .
0.0006
0.0003
o L-_~_-L_~ __ L-_~_-L_~ __ L__~_~
o 480 960 1,440 1,920 2,400 2,880 3,360 3,840 4,320 4,800
t (5)
11
o 0
Test 11
0.072
0.084
0.056
0.048
0.04
0.032
0.024
0.Q16
0.008
O~~~--L---L-~--~-~--~--L-~-~
o 480 960 1,440 1,920 2,400 2,880 3,360 3,840 4,320 4,800
t (5)
11
o
Test 11
Appendix 4 Files in Table 14 49
56,000
52,000
48,000
44,000
40,000 L -_ _--'---_ _--'-_ _----'-_ _- - - ' ' - -_ _-'--_ _--'-_ _----'-_ _- - - ' ' - -_ _-'--_ _- '
o 480 960 1,440 1,920 2,400 2,880 3,360 3,840 4,320 4,800
t (s)
11
o
Test 11
57,000
54,000
00
..................................................................... ··DO ..........................................
51,000
00
00
48,000 ················································0 "tiUD ··················································...........
39,000 '--__..L.-_ _- - ' -_ _- - - '_ _ _ _- ' - -_ _..L.-_ _- - ' -_ _- - - '_ _ _ _-'---_ _..L.-_ _- '
o 0.008 0.016 0.024 0.032 0.04 0.048 0.056 o.~ 0.072 0.08
W (rn'3 )
11
o
Test 11
Appendix 4 Files in Table 14 50
0.84 .......................................•.....................................................1;;1............ .
0.56
0.48
0.4 o
........................................................................ ·n·············································
0000
0.32 ........................................................... ···········8·········································· ...... .
0.24
o 480 960 1,440 1,920 2,400 2,880 3,360 3,840 4,320 4,800
t(s)
11
o
Test 11
900 ........................................................................................................................... .
800 D
.......................................................................................................................
o
700
o
600 ··················································0··............ D 00"·····:g····································
500
DD ODDOD
400 •.... CL ...........................................................................................................
300 .•.....•......•...••.....•...•....••.•........•......•....•.•..•......•.....•....•.•....•....•.•..........•........•.•...•.•
100 .•..........•.•...••.....•....•....•.•....•...•......•....•.•..•..•..........•...•.•..•.•....•.•..........•........•.•.....•
o 480 960 1,440 1,920 2,400 2,880 3,360 3,840 4,320 4,800
t(s)
11
o
Test 11
Appendix 4 Files in Table 14 51
0.0012 . ·····8···············································...............................................................
o
0.001 BflB-···G················································ ............................. .
o
0.0008 ........................................ . ........................................................................ .
0.0002 ..........................................................................................................................
O~ __ ~ __ ~ ____L -_ _ ~ __ ~ _ _ _ _L -_ _ ~ __ ~ ____ ~ __ ~
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t (5)
i2
o
Test 12
0.054 -- ------ --- ------- -- --- ------ --- -_._._ .. _.- ----._ ..... -.-.... -.. -._.-......... -...... -... __ ... --_ .. __ . _.. ----- . ------ --
0.048
0.042
0.036
0.03
0.024
0.018
0.012
0.006
O~--~----~----L---~----~--~L---~----~--~
840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t (5)
12
o
Test 12
------ ---------------------
144,000 ---------_.-----.-----------------.---------------------------_.-------------------._------------------"'--:-U::V'
138,000
132,000
126,000
120,000
102,000 ~@:------~-----------------------------------------------------------------------------------------
96,000 b~~_ tl'___:=
_________________________________________________-----------------------------------------------------------
90,000 "----_-L-_---'--_-----'_ _-'---_---'--_-----'_ _-'-_-'--_-----'_---'
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t(S)
12
o
Test 12
126,000
120,000
114,000
108,000
102,000 ----------------,::r----~~-,.,t::-----------------------------------------------------------------------------------
96,000 ~- --------------------------------------------------------------------------------------------------------
90,000
84,000L---L-----'--------'L---L-----'--------'---'---'--------'----'
o 0.006 0.012 0.018 0.024 0.03 0.036 0.042 0.048 0.054 0.06
W(m3)
12
o
Test 12
Appendix 4 Files in Table 14 53
0.72
o 0
--_ .. ---------_._._--------------------------------_.--------------------.--_.-.-------- ---------------------_._----------
0.6 ................................................... g..................... ................................................
o
0.48
0.36
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t(5)
12
o
Test I2
1,800
1,500
1,200
900 ..·q
blfB~:twll! ...~
..·tl.:.:: ..........................................................................................
600 .......................................................................................................................... ..
300 .......................................................................................................................... ..
o 840 1,680 2,520 3,360 4,200 5,040 5,880 6,720 7,560 8,400
t (5)
12
o
Test I2
Appendix 4 Files in Table 14 54
00
~'1I!ilh....................................................................................................
0.0006
0.0004
o
0.0002 ......................................................................................................................... .
o 960 1,920 2,880 3,840 4,800 5,760 6,720 7,680 8,840 9,600
t (5)
i3
o
Test I3
0.032
0.028 ........................................................................... .. ......................................... ..
0.024
0.02
0.016
0.012
0.006
0.004
o~_-L_~ __ L-_~_-L_~ __ L-_-L_~_~
o 960 1,920 2,880 3,840 4,800 5,760 6,720 7,680 8,840 9,600
t (5)
13
o
Test I3
Appendix 4 Files in Table 14 55
240,000
220,000
180,000
160,000
140,000 \d-----'----'-------'-----'----'------'-----'----'-----'------'
o 960 1,920 2,880 3,840 4,roo 5,760 6,720 7,680 8,640 9,600
t (s)
13
o
Test I3
180,000
140,000 '-Y-----'-----'------''------'------'-----'-----'------'-----'-----'
o 0.004 0.008 0.012 0.Q16 0.02 0.024 0.028 0.032 0.036 0.04
W(m3)
13
o
Test I3
._------
0.84
0.72
0.6
0.48
o 960 1,920 2,880 3,840 4,800 5,760 6,720 7,680 8,640 9,600
t(s)
13
o
Test I3
1/J (s/m) Intermediate Blocking Model
4,000 r - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - ,
3,200
2,800 ............................................................................. .......... Q ............................. .
2,400
o 0
o,····EJ· .... ··· ....·.... ··..........·....·............·· .. ···
2,000 ~~·?f··G ...... · .......... ··· .. ·· .... ··· .... · .. ···· .. ···· .... · ...... · .. ·· ...... · ......
1,600 ~iihIIli~I!«!I1::-
..·..I .................................................................................................
1,200 ....................!J2.................................................................................................
800 ........................................................................................................................... .
400 ........................................................................................................................... .
o 960 1,920 2,880 3,840 4,800 5,760 6,720 7,680 8,640 9,600
t(s)
13
o
Test I3
Appendix 5 1
Notes
The values in "Flow rate" and "Solid conc" were measured during the tests. The
values in "Bulk velocity" corespond to U in Tables 20 to 23.
The values in the item "Base pressures (in, filt, out)" were calculated from Figs
*** and *** in BAR. They might be the values in the items "Inlet pressure" and "Outlet
pressure" if they were higherthan those displyed by the pressure gauges during the tests.
The values in the item "Pressure (by inlet, outle!)" normally equal to the value of
per(meate) side, but they may vary if the outlet valve has been throttled.
The values in the item "A verage TMP" in Pa refer to the P, in Tables 20 to 23.
The values in the item "Membrane resistance", and those in the last row of items
"Flux corrected" and "Deposit res'ce" refer to Rm, J.,and Re in Tables 20 to 23
respectively.
The methods of calculating the values in items "Flux raw data", "Viscosity" and
"Flux corrected" have been explained in Chapter 5.
f ' ''":0'
, ~ •• Ij. ·1
,
NORMAL File : FN31617N
than 2000 particles per ml. grea ter than 2 I'm and abso- '"
lute filtration at 5 I'm. The solids need to be removed j )(
from the water to prevent deposition and blockage, •
~
within the pores of the oil reservoir rock during the ! '" silica
water flood as well as to protect injection equipment.
§
u "
The volume of water required in the water flood can be
as high as 2600 m3 .hr' (400000 barrels of water per ,'"
'"
,,~ ,,~
day), for a field and is rarely less than 650 m3.hr'. Deep
bed or cartridge filters are used at present. Particle Size, microns.
Nature of seawater. North Sea seawater used in reser-
voir injection is reasonably clean, containing between As 1. Size dlll1rlbu1lon 01 solidI In ... w.'.r and alllca.
0.2 and 0.8 mg.l·' of suspended solids and it is usually D,
pumped up from a depth of200 ft. (6Im).
The major contaminants are clays, sand, bacteria and CODeenlnt. .,
plankton which are usually filtered out in the deep bed Po
or cartridge filters. The seawater solids loading is
highly seasonal; blooms of plankton occur in the spring 'ubuler Crollflow filler
and autumn and during these periods the suspended
solids content is increased considerably. It has been 0.1 I'm MUllpo,.
reported that the major cause offouling of the seawater Deed-ended
ftlter cartridges is due to the lipid content of plankton'" filler
which is released into suspension when the organisms
are crushed by the pumps and filters. The resulting
,. Cornpuler
Tenlr: ".
lipid concentration can rise to as high as 20 mg.l" dur-
ing a bloom period. The lipids are fatty materials which
act as a glue; sticking the suspended solids to the filter
surface thus encouraging blockage'''.
Experimental
Challenge suspensions. Figure 1 shows the particle size
distribution of suspended solids measured in sea-
water''' and the size distribution of the silica material
. used to make the challenge suspensions for the labora- t "
tory tests. The lipid tests used fish lipid concentrate cap- Flow
sules with eicosapentaenoic and docosahexaenoic acids, Me!.r
purchased from Boots the Chemists Ltd.
Membrane types and rigs. The initial rig was con-
structed out of PVC and was designed to accommodate "y. '.
the sheet membrane in a plate and frame fashion Ul • The ..
.,'
The second rig, developed much later, was built to Feed liow rale 4 Um
commodate both tubular and capillary membrane ••• • pressure 0.21 Bar
><Iules. This is shown schematically in Fig 2. Both rigs fibre 97
,ve electronically controlled solenoid valves, described
follows:
j
••
• •••
.
fibre 98
E
v, is responsible for controlling permeate flow from It
the filter. • -; B
v. is used to control the flow through the rig clean·up ~ fibre 99
filter (Millipore O.l1'm cartridge). .~
V3 controls the 'outlet pressure from the filter.
v. is responsible for controlling the filter backflush.
a
\
le clean.ult filter was only used to remove suspended
aterial from the tap.water prior to commencing an
:periment. During crossflow filtration v. was closed.
•
"Or. 98
" fibre 97
•
---
M•• n merntune pressure. S.,.
u
FIg 3. Wator nux rale.ln tubular and caplllery membran". fibre 99
Backflushing with compressed air was employed to
ean most of the membranes and the period between,
od duration of, backflushes was controlled by the corn·
" " " .. so .. '"
• ter program. Particle m6nitors were also developed Filtration time. minutes .
od employed on the filter feed and filtrate lines to FIg4b. Flux rate. with metal IIbre nltera.
,eck the quality of the water. (Re 0142 500).
An Enka 1.8 mm capillary membrane and tubular
letalfibre membranes were tested using the above rig.
he clean water flux rates for these membranes are The particle retention was measured by taking a
Iven in Fig 3. The fluxes shown were obtained from sample stream from both the filter feed and filtrate
10s using a variety of crossflow rates ranging from 4 to through a model 346BCL Hiac Royco particle detector
) Vmin through the filter (8 500 < Re < 42 500). This fig. and counter. This enabled the number of particles in
re demonstrates that, up to a flux rate of 6m'.m·'.hr ' , suspension, down to a particle size of 0.72 I'm, to be
.e permeate rate which is a unique function of memo measured. The retention efficiencies are tabulated
rane pressure, was independent of crossflow velocity. below.
his can be true only when filtering clean water. The
lembrane resistance (R,.J can be calculated from a re· Filter Flow Retention efficiency (%) In grade !I'm)
lTanged form of Darcy's Law as follows: No 'rate
Totalllow 96l1min.
i mean pressure 0.7 8ar. "-
• • •
J
! iE
.
u 2mgJI
~
J ·
,
u: lipid
,,
" " "
. "
Filtration time, minules. Filtration time. minutes.
FIg 5. Rux from the Versapor 3000 membrane. Fig 6b. Perme.te nux rate at 10 mg/l olllpld.
...,.
, mgJI
tions were tested: 5, 10 and 20 mg.!·'. Before the lipid
was added to the membrane system the flux rate
obtained during the filtration of clean water, and
2 mg.!·' silica suspended in clean water, was checked.
The lipid was added to the system after the second fll- " " " . "
tration, hence the suspended solids concentration dur- Filtration time, minules.
ing the lipid tests was also 2 mg.I-'. This is still a
relatively high concentration of solids for ofTshore sea- FIg &C. Perm.ate nux rat. at 20 mg/l 01 lipid.
water filtration. The results are shown in Fig 6.
• ..
I,,,,, u
"
,;
,•
..
u
Fillration time, minutes. l u
u X
operating at a mean membrane pressure of 1.2 Bar, is "
·~ ..
' mgJI
between 5 and 7 m'.m·'.hr l Increasing the lipid concen-
2
"
tration decreased the membrane flux rate and caused ~
" lipid
the flux to decay more rapidly after backflush. 02
Backflushing with compressed air at 3.5 Bar restored oi,
acceptable membrane flux rates, even on filtering a sus- " " " " "
pension containing 2 mg.I-' of silica and 20 mg.!·' of Filtration lime. m.nvtes.
lipids.
After each of the above tests the membrane was Ag 7. Permeate.flux rate at 5 mgll of lipid.
removed from the filter holder and washed in solvent to
dissolve the fish oil, in accordance with the technique Enka capillary. Figure 7 shows the results for the
given by reference 4. The masses offish oil measured on same test suspension used with the Enka polypropylene
the filter, and the measured concentration of oil in the membrane at a lipid concentration of 5 mg.I-' and a
feed, are shown in Table 2. mean membrane pressure of O. 7 Bar. This membrane is
Filtration &: Separation MarchiApui 1991 119
PROCEEDINOS OF THE FlLTRAnON SOCIETY
>d at 0.21'm pore size and is made out of a hydropho- with dead areas in the feed channels towards the
,bic material. Before use the membrane has to be periphery of the filter plate.
'. with a low surface tension liquid. for example. In addition. chemical resistance to both seawater and
A. and backflushing with air cannot be employed for membrane cleaning fluids must be considered.
mbrane cleaning because it would be necessary to Filter unit size. The required 400 m' of membrane area
'et the membrane aner backflushing. A water back· could be provided by a se.ies of membrane modules
;h was therefore employed using a pump delivering a operating in parallel. To provide an indication of the
:kflush pulse of 2.8 Bar. . overall filter unit size this can be calculalpd for the
;omparing Figs. 3. 6 & 7 shows that the clean water Enka membranes as follows. The largest module corn·
< rate is lower for the Enka membrane than for the mercially available has 10 m' membrane area. there-
tal fibre ones. but the average flux rate during the fil· fore 40 modules would be required. The dimensions of
tion of a lipid containing suspension is similar. such a module are (width by height): 0.15 X 1.0 m.
Allowing for access space arr.und the modules and for
rsapor 3000. Figure 8 shows the flux obtained from extra modules to act as standby units. a typical cross·
~able lipid concentration test suspensions challeng· .
flow filter unit would be 1 rr. long. 2.5 m high and 2 m
:this membrane at 80 l.min·' feed flow rate and mean / wide. This would require a floor area of2 m'. The mate-
mbrane pressure of 0.7 Bar. Also shown on this fig· rials of construction are polymeric are hence light-
~ are the flux rates using tap-water and a 2 mg.l· 1 sil- weight and the resulting filter unit is, therefore. both
concentration. compact and light-weight.
Bacl\Oush at 3.5 Bar
1
• ConclUSions
"
. -M
•
.......
Seawater is a relatively clean process fluid to filter. for
most of the year. Under these circumstances flux rates
of up to 5m3 .m'.hr·' can be achieved. with a membrane
pressure drop of 1 to 2 Bar. During a bloom period. how·
.......
+
ever. flux rates could easily fall below 1 m 3.m·'.hr'.
.. • • .......
c
Under these conditions frequent cleaning is needed in
order to maintain a flux rate of between 1 and
l :
2 m3 .m·'.hr'- This cleaning can be achieved by back-
.~
M
10 ...... flushing the membrane with air or water.'
Under the conditions reported above the polymer
I
• .. " " "
membranes were not more seriously affected by the
•• " presence of oils in water than the metal membranes and
Filtration time, minU1es. flux rates during the filtration of oil containing suspen-
sions appears to be fairly independent of membrane
FIg 8. Permeate flux rat. at variable lipid concentration type. This can be explained by the formation of a
dynamic or secondary membrane on the surface of the
fIXed membrane. consisting of the suspended material
.mparison of membrane types. The three different within the water. After this has formed. further filtra-
,mbrane types: tubular. capillary and sheet. give sim· tion is controlled by the resistance and rejection capa-
r flux rates when operating on lipid containing. and bilities. of this dynamic membrane.
~hly fouling suspensions. Backflushing with air or The choice of the most appropriate membrane type
,ter was successful in maintaining reasonable perme· for the crossflow filtration of seawater does not. there-
, flux rates. The most appropriate membrane for sea- fore. depend on flux and rejection capabilities. but on a
Iter filtration for offshore oil-production depends on multitude of other factors such as ease of cleaning.
ler factors which may be important. The most impor- membrane packing density and robustness.
ot of these are summarised below:
Membrane packing density. - Th provide 650 m3.hr'.
apprOximately 400 m' of membrane area is required; Acknowledgements
sheet membrane can be packed most tightly and The authors of this paper wish to record their gratitude
tubular membrane the least so. for a Science and Engineering Research Council grant
Cost. - Metal fibre tube is the most expensive whilst to support a project of which this work formed a part.
polymer is the least expensive. The project is administered through the Marine
Technology Directorate Ltd. and is also supported by
Conuenience. - Capillary membrane modules can be the following: BP Exploration. Texaco. Arnoco. Chevron.
easily replaced on the rig. requiring minimal labour. Occidental. Elf. Marathon. Hamilton Brothers and
On the other hand sheet membrane is time consum- Unocal.
ing to replace.
Operating pressure. _. Increasing the membrane
press,!re increases flux. The polymer membranes References
are limited to pressures of around 2 Bar whilst the 1. Carter. A. J., An Experimental Study of Crossflow Filtration
metal tubes can operate up to 10 Bar. and the Design of a Prototype Crossflow Filter, M. Phil. Thesis.
Loughborough University of Technology l1982).
Membrane antifouling techniques. such as cleaning 2. Knibbs, R. H.. The Development of a High Flux Microfilter
the membrane with a D.C. current can be applied to with a Wide Range of Applications. Filtech 81. London (1980.
metal membranes. Filtration Society, pp 59,68.
Coarse filtration. prior to membrane filtration. can 3. Abdel-Ghani. M. S., Janes. R. E. and Wilson, F. G .. Crossflow
be avoided with the metal tubular membranes. thus Membrane Filtration of Seawater. Filtration and Separation
11988). pp 105.109.
saving further space and weight on an oil rig.
4. Edyvean. G. J. and Lynch. J. L.. The Effect of Organic Fouling
There is evidence to suggest that the flow distribu- on the Life of Cartridge Filters, Filtech 89, Kaclsruhe (1989),
tion in the plate and frame membrane filter is poor. Filtration Society. pp 10,17.
Filtered seawater is used in the offshore oil industry for both topside duties such as cooling and
for injection into oil reservoirs to displace the crude oil. It is filtered to prevent damage to
equipment and blockage of the reservoir. The required filtrate rate can be substantial. Various
cross flow filter designs and geometries for this duty have been studied, both in the laboratory
and at a seawater test centre. Organic fouling of both microfiltration and ultrafiltration
membranes was apparent, with high average flux rates obtained only when it was possible to
mechanically remove the fouling layer. The calculated membrane resistance was also shown
to increase with fouling and was dependent on hydrodynamic conditions. Thus membrane
resistance must be determined in-siru when modelling similar crossflow filtration syste~s.
INTRODUCTION
There are several industries which use seawater, one of the largest being North Sea oil production.
Oil lies within the pore spaces of a rock, normally sandstone, and water is used to displace oil
from the reservoir by pumping under considerable pressure. The seawater is often filtered to
remove suspended material which would otherwise "filter" out within the rock formation. This
would eventually lead to clogging of the reservoir. Some production platforms now employ
Reverse Osmosis (R.O.) on the injection water to reduce the concentration of sulphate ions
present, thus reducing the precipitation of barium sulphate in the rock formation.
Filtration is also employed to protect equipment which uses seawater on the oil platform: R.O.,
water sealed pumps, cooling, etc. On some platforms over 50% of the water drawn up from the
sea is used for duties other than injection. The total flow of filtered water can be over 750 m 3.h· l •
Fine filtration is achieved at present by means of deep bed or cartridge filters. These perform
quite adequately over a large part of the year but frequently become clogged by the seasonal
algal blooms. On an offshore platform space and weight are at a premium and any new technology
which could reduce these and overcome the seasonal variation is beneficial.
19
Water used for cooling water duties is at present filtered on 80 IlIlI coarse screens, whereas the
injection water is filtered so that less than 2 t03 thousand panicles per ml greater than 21l1l1 are
present.
IIlboratory trials
The initial trials have been reponed elsewhere (1), and were conducted to identify membrane
types which might be suitable for further tests. Some of the factors of major importance which
were assessed included panicle retention size, filtrate flux rate, chemical compatibility with
seawater. Various different geometries were evaluated, including capillary, tubular and flat
sheet membranes. A brief description of the membranes used in this phase is included in the
appendix.
The ftrst problem with any laboratory test is to identify a suitable challenge suspension for the
filters; one representative of the end use. The challenge suspensions employed were as follows:
i) tap-water,
ii) silica solids all sub 20 J.lIll with dso of 7 J.lIll in tap-water,
iii) above plus lipids, and
iv) seawater algae suspensions.
Solids concentrations up to 10 mg.rt, and the lipid concentrations to 20 mg.r 1 were used. The
presence oflipid material has been identifted as the major cause of membrane fouling in seawater
filtration (2), and concentrations up to 20 mg.r 1 are very high. Filtration performance of the .
most suitable membranes, using the ftrst three test suspensions, are summarised in the appendix.
Tests were conducted with membrane types other than those shown, such as adynamic membrane
system (3), a tubular sintered metal powder membrane and a polymer depth filter. The last two
types of filter both suffered from irreversible clogging of the media, a consequence of the depth
filtration mechanism. All the membranes in the appendix produced a fIltrate of acceptable
quality in terms of number of particles above 2 J.lIll. Filtrate fluxes were reasonably similar
under similar flow conditions due, possibly, to the formation of a dynamic or secondary
membrane, and further tests at a seawater test facility went ahead with the metal and ceramic
filters. The polypropylene membrane was not tested because it needed wetting prior to use and
could not be allowed to dry out during operation. This was thought to be an unacceptable
operating complication in this industrial process.
Further laboratory studies were conducted on a small (0.05 by 0.51 m), sheet membrane system
to investigate the effect of increasing membrane resistance during filtration, and different flow
conditions. Versapor 0.21l1l1 membrane and Bekaert "3 AL 3" metal membrane were used, and
a challenge suspension containing Dunaliella tertiolecta (CCAP 19/6B); a seawater algae
cultured from a Norwegian Fjord. The challenge suspension concentration was approximately
1 mg.r 1, and the size distribution is shown in Figure 1.
lOO
I- 80 ~
•
N
1 80
I
/
I
~
•
.~
.c
,"
3 20
/
0
o
./5
,
10 15
,
20 25
,
30 35
Particle lize. mictona.
20
Membrane resistance during filtration was calculated according to the "cake" filtration theory
as applied to microfiltration:
(1)
where J is filtration flux. tJ.P is transmembrane pressure. ~ is viscosity and R.. and R. are
membrane and deposit resistance. respectively. The membrane resistances. determined in-situ.
for the metal membrane are shown in Table 1
Table 1 Metal membrane resjslances during crossflow filtration
21
·.... , - - - - - - - - - - - - - - , -.-----------------,
...............~~. ~.~~.~ ..
12400 ,.j
S:S=
.- ------------ ..... _-_ ..... _- ...-.-- .. ---.. -.~-.- .-._--._ ... ~IOO • ••••••••••••••••••• Ra.75O() •••••• .Ba .10ll0Q •••••••••••••••
=
.§
i! Re 2500
.---_.-._- .............. ... _- ........ . [tIOO
Re 2500 Re 7500 Re 10000
• L-_~_~
o • ~
__
•
L-_~_~_~
•
FIltrmon time. miruAes.
t. ~
.~.-~~~--~.--~.~-~.~~.~.~~
Fdlration time. minules.
..
Figure 2 Fjltration of seawateT al gae on Figure 3 Filtration of seawater algae on 02
metal membrane !lID polymer membrane
The presence of algae did not affect the metal membrane resistance. The polymer membrane
resistance in the presence of algae is significantly greater than without it. Table 2. It is also
noticeable that increasing pressure increased the polymer membrane resistance. and increasing
the shear rate on the surface decreased it. Clearly. some suspended material remained after
filtering the tap-water which then deposited on the membrane surface. All the above resistances
are membrane resistances only. Le not including the cake or deposit resistance. It is this deposit
which must mechanically combine with the membrane to provide a new membrane resistance.
Membrane resistance cannot, therefore. be assumed to be constant and equal to that given by a
clean water permeation test It must be determined in-situ. a similar situation to that of classical
cake filtration. Further evidence of the intimate relation between the membrane and deposit,
and of the reason for the different membrane resistance performance of these two filters. is
shown in Figures 7 and 8. Further discussion is left until that Section.
sea water trials
The membrane filters that showed promise during the initial laboratory trials were taken to a .
seawater test facility for further trials. These ran over late August and September 1990. This
was not a bloom period. Nine samples of seawater were taken throughout the tria! period, and
the Coulter Counter analyses for these are shown in Table 3.
Table 3 Seawater Particle Size Distribution and SoUd
Concentration duDn g trial period
22
Variation in the trial fluid is inevitable when undenaking field trials, bUI the variation between
samples shown above is nOI substantial. Meaningful comparisons between the filter performance
can, therefore, be made.
During all the trials a mean ttansmembrane pressure of 1.1 Bar was maintained. It was not
possible 10 lest under identical conditions of Reynolds (Re) number, however. The flux curves
shown in Figures 4 to 6 were obtained by continually monitoring the filtrate rate by a "litre
meter" connected 10 a chart recorder. Bacldlushing at pressures up to 5 Bar was tested during
the trials but it was found 10 be ineffective in all cases except in the presence of a membrane
precoat, this will be discussed later. Chemical cleaning of the membranes was also investigated.
both on site and back in the laboralory, bUI this was also discovered to have little effect in
restoring the initial membrane flux. The chemical cleaners used were solutions of 5% citric
acid, UltrasiJ 50 and Ultrasil 11. Thus the fouling was deemed to be irreversible.
..... ~r---------------------------,
4000 --- ---- ______ ---- ____ ---- --- _.0 __ ••• ,0 •• _____ .0 ____ • u . . . ___ • ____ _
10.000 ."
:- r ."-
.~
....ti 1,000
i!
i: :s:':'
:::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::::
~
- ',01»
." 100 Loo_ •• _____
r
••••• _________ •••• __ • _________
o~o--~.~-~=-~.~-=.--~,~.--~,.~~~~~,.
Cl.CfIlo......2aQQ •••
FiM'l4 Filtrate flux rate for variQUS FiM'l5 Ceramic membrane flux
membranes oyer scyernJ days
60,000 r----------------------------------,
All Falrey Rlter Tubes 2.000
50.000 14 mml.d.
.,.
,:",
.c: 40,000 1.500
.
El
E
..J ~
{30.ooo 1,000
r3
.~
>< ~
~ 20.000 .:.
precoated 500
10,000 - __ Re 7700
o L____-L~=-~~===i:===~R~e~170~4~O 0
o 0.5 1 1.5 2 2.5
Fi ~ration time, hours.
Fi~re 6 FUtrale flux rale for metal membrane with and without preCOat
Figure 6 shows the effect of mixing dicalite speedplus with seawater, filtering at a concentration
of 0.5 g.r' and then inuoducing seawater at a solids content of 1 mg.r', i.e a precoated filtration.
After precoating the flux then decayed in the same manner as the other filtrations shown. After
2 hours, however, a bacldlush resulted in a flux rate in excess of 30,000 l.m·2.h·t, which
. subsequently decayed to 400 J.m·2.h·'. Bacldlushing was not effective in restoring flux in any
other filtration. Clearly, the precoat protected the metal membrane from intrusion of fine
23
suspended material and irreversible fouling. A new metal membrane filtertube, without precoat,
is also shown in Figure 6, flux decaying from over 50,000 to 400 l.m· 2 .h· l • Backflushing did
not restore the flux in this instance.
DISCUSSION
Comparison between the above figures and the appendix shows that average fluxes in excess
of l()OO l.m· 2.h· 1 can be achieved in the presence of inorganic material using backflushing. Similar
flux rates have been claimed for other membranes operating on seawater (4). At low
concentration of inorganic material backflushing is ineffective and f1uxes reduce to below 100
l.m· 2.h· l • Scanning Electron Microscope (SEM) photographs of the fouled membranes from the
sea water algae runs were taken to determine the form of the fouling present on the membrane
surface. These are reproduced in the figures below.
i,
..
;
,
24
Fjgure 8 Metal membrane filter clogged with a1~ae and soUds
These photographs assist in the interpretation of results included in Tables I and 2. Large flow
paths remain open in the metal membrane both in the presence of algae and without it. The
membrane resistances are, therefore, similar and fluxes in the order of 400 l.m·2 .h· l result. Such
large flow paths never existed with the polymer membrane, and clogging easily occurs, giving
membrane resistances an order ,of magnitude greater than for the metal membrane and flux rates
approximately one half. Polymer membrane resistance decreased with shear, or Reynolds
number, but irreversible fouling occurred with both membranes.
CONCLUSIONS
Average seawater fluxes in excess of l()()() l.m·2.h· l can be sustained if it is possible to dislodge
the surface deposit. This could be achieved in two ways. Firstly, by the use of a precoat, which
could prove expensive or unacceptable from environmental standards. Secondly, by the use of
an open structured membrane with surface pores which are too wide for the gel layer to form a
sa-ong mechanical bridge on. Under these circumstances the use ofbackflushing, or a mechanical
means of membrane cleaning, would be effective for restoring flux. Fine material would,
however, pass the filter. There is considerable variation between the operating companies as
to the level at which filttation should occur, but it is likely that injection water not subject to
R.D. will only be relatively coarsely filtered. say 10 J.UI1. A crossflow filter could be used for
this and. under these circumstances, the coarse filttation stage could be removed. Should fine
fila-ation be required a small cartridge filttation stage could be used to polish the filttate. The
coarse crossflow filttation stage would protect the cartridge filters during a period of algal bloom,
when the suspended solids content rises and, paradoxically, efficiency of crossflow filttation
improves.
Filter geometry does not appear to be significant in detennining flux rates, nor does filter type.
This is a consequence of the dynamic or secondary fouling layer. Thus the choice of filter type
can be made on the basis of other operating criteria, such as: membrane packing density,
2S
replacement ease, ruggedness and cost. A plate and frame crossflow filter containing sheet
membrane is one of the most suitable designs. Very careful attention to flow distribution is
required with this type of filter, however.
It is often the case that cross flow filtration is tested as a means of filtering a process suspension
that is otherwise difficult to filter. This leads to poor results and, therefore, rejection of the
technique. This is sometimes due to a poor understanding or control of the process, or
unjustifiably high expectations. This work has shown that good filtration performance can be
achieved when filtering suspensions of high mineral content using a mechanical membrane
cleaning technique. Suspensions of low mineral content facilitate the penetration of the
membrane with organic material which causes irreversible fouling. Strategies have been
suggested to prevent such fouling. These strategies are now being investigated.
ACKNOWLEDGEMENTS
The authors of this paper wish to record their gratitude for a Science and Engineering Research
Council grant to support a project of which this work formed a part. The project is administered
through the Marine Technology Directorate Ltd, and is also sponsored by the following: BP
ExploTlltion, Texaco, Amoco, Chevron, Occidental, Elf, Marathon, Hamilton Brothers and
Unocal.
REFERENCES
1. Holdich, R.G., Zhang, G.M. and Boston J. "Crossflow Filtration of Seawater", World
Filtration Congress, Nice, France (1990), pp 518, 522.
2. Edyvean, G.J. and Lynch, J.L. 'The effect of organic fouling on the life of cartridge fllter",
Filtech 89, Karlsruhe (1989), Filtration Society, pp 10, 17.
3. Holdich, R.G. and Boston, J. "Microflltration using a dynamically formed membrane ",
Filtration and Separation, 27 (1990), pp 184, 187.
4. Goodboy, K.P. and Louy, G.C. "Operational results of crossflow microfiltration for
produced and seawater injection", Water Management Offshore, Aberdeen (1989). mc
Technical Services Ltd.
26
APPENDIX Remits of laboratorv crOssflo:.l! filtrations
27
527
CrossBow micro6ltratioa filttate flux rata ban been enIumced by the iDcorporatioD of rotational ftuid Oow arouod the surface of
the filter mem.braDe. 1be rotatiouaJ Ouid Oow induced a ceotrifogaJ field force OD the suspeoded material which acted in the
opposite direction to the liquid drag, thus membrane fouling was reduced. Tbe rotation "lIS induced by means of filter module
boIdn geometry, aDd by JDCaII5 of. beIkaI insert causing the 80w to rotate. Experimental results show that an energy saving of
20-;' is possible using this system compared with ODe in wbicb DO rotational 80w existed.
0263-8762/92/$05.00 + 0.00
© Institution of Chemical Engineers
528 HOLDICH and ZHANG
Filter
Inlet Outlet
0.1 ~m filter
Tank
6mm
Figure 2a. Endcap showing entry and exit flow normal to filter mem- Figure 3. Schematic diagram of the crossflow filter experimental equip-
brane. ment.
2.'
2.0 3.S
'i
!!!.
!!
,.
~
ill '.0
!!
a. '.S - - -----!+---+(
o.
0.' L._-:-~_---:~_---:~_---:=-_---:~_---:!.
0 o 1000 2000 3000 4COO sooo
0 0.0. 0.11 0.25 0.33 0.42 Filtration time (s).
Flow rate (in3S·'}X1000. Hallda T~ c-nM:l
24 10 a cIeg c: Ibing " 2S cIeg C
Normal
-e- Heb
-'tt- T~ ----e---; -~- 0
Figzue 4. Inlet pressures as a function of feed ftow rate for different Figure 6. Permeate flux rate decay with time and the clTcct of variable
cndcap and filter types. temperature.
resistance, temperature fluctuation, lack of accurate and a technique to quantify the in situ deposit resistance
knowledge of the filtration pressure, size and density is required.
segregation of deposit on the membrane surface, surface In conventional constant pressure filtration the square
charges, lack of homogeneous membrane, etc. The fol- of the volume of filtrate produced is proportional to
lowing procedures were followed in order to eliminate filtration time, and the filter medium resistance can be
some of these variations. calculated from the experimental results by some simple
Variation of permeate flux rate with temperature was algebraic manipulation. In crossflow filtration no such
corrected using the viscosity difference between water at simple relation between time and filtrate volume exists,
the measured temperature and a reference temperature thus an alternative method must be used to calculate the
taken to be 25°C. Thus all the flux rates were corrected to in situ membrane resistance. Such a method is to consider
that which would have been obtained at a temperature of the initial stages of filtration, taking a tangent to the
25°C. This is shown in Figure 6, where the flux rate (J.) volume filtrate against time curve to provide a value for
under conditions of rising temperature has been con- J w, which is then used in equation (2) to provide a value
verted to one equivalent to that at 25°C (J 2.) using the for membrane resistance. An example of this for one
following equation: filtration is shown in Figure 7. Membrane resistances
were calculated for all the filtrations by this method,
1'. these are given in Tables 1 and 2.
J 2 • =-J. (I)
1'2. Also shown in these tables are deposit resistance which
where 1'. and 1'2. are viscosity at the measured tempera- were calculated by applying that Darcy's law after equi-
ture and at 25°C respectively. librium was reached. The two resistances due to the
A duplicate run is also shown in Figure 6, where the membrane and the deposit are assumed to be additive,
temperature was maintained at 24 to 26°C. From this thus:
figure it can be seen that correcting the experimental data (3)
for rising temperature gives a similar result to one
obtained under conditions of constant temperature. The where J, is the equilibrium flux rate.
very slightly larger values of flux rate after conversion, It should be noted that Rm is assumed to be a constant,
compared with that obtained by maintaining the temper- but R d ,,,,,,,, is a function of filtration time until the
ature, can be explained by the slightly higher initial equilibrium flux rate is achieved. Darcy's law is then
permeate rate, i.e. the slightly lower membrane resis- applied to determine the equilibrium value of the deposit
tance, in the experiment in which the temperature in- resistance using a rearranged form of equation (3).
creased. This experiment validated the use of It should also be noted that the values of membrane
equation (I) to correct filtration flux rates in the other resistance in Tables 1 and 2 include a contribution due to
filtrations where temperature fluctuation occurred. the solids that initially penetrate the membrane surface.
They are, therefore, much higher than the membrane
resistances that would have been obtained by means of
Membrane resistance clean water permeation tests.
It is the intention of this work to be able to compare
In membrane studies involving modelling, or compar- the effects of filtering in a rotating flow field and without
ison, it is common for the membrane resistance to be such a field. In order to conduct this comparison, any
determined by the use of the clean water permeation rate effect due to the variable nature of the membrane resis-
(Jw)' The membrane resistance is given by Darcy's law: tance must be removed. The lowest membrane resistance
!l.P in Tables 1 and 2 is 1 X 10' m-I, thus the data for the
R =- (2) remaining filtrations has been 'normalised' to this mem-
m iJJw
brane resistance. The most straightforward way of
where !l.P is the pressure across the membrane and Rm is
the membrane resistance. It is often assumed that the
membrane resistance remains constant and equal to the
clean water value during filtration, thus any increase in " ,/
,-extrapolation of
initial rate
resistance during filtration must be due to the deposit.
...s.
0
This approach is not valid in conventional cake filtration 8
for the estimation of filter cloth resistance, and it is "
unlikely to be accurate in microfiltrations in which the
suspended particle size is close to, or finer than, the pore
size of the membrane, such as in this study. Under these
..E ..
¥J
u
-'-
u
'=
"
"s
" ..
• "e
1- . •
§.
~
~x ... o
1!x ~
~
, ,S •• o
s,
~
.c
·c
,g
"5.,.
...
:sw.,. w
•• G.2 0.. 0.6 0.8
Pressure across membrane (Bar) .
•• ~ 0." 0.. 0.' 0.81 1.00 1.11 1.• ' 1.61
Pressure across membrane (Bar). 6 0 ~ • •
s' ).
------ --.......
NarmaI HeIcaI
._-...-
T~
Axial velocities (m
"r-------------------------------------,
...
"
's
"§. o.
~
1!x ..
~
S, •..
~
_T_
w • ... u u u
•• 02 0.. o.S 0.'
Pressure across membrane (Bar) .
Pressure across membrane (Bar). ~ 1~' ~ l~t
holder and some flux rate dependency with crossflow centrifugal acceleration at the membrane surface using a
velocity can be observed. rearranged form of equation (7):
Flux rate is usually a function of crossflow velocity or
shear rate. The lack of such a relation in the case of the rro , = 181'1 (8)
normal filter holder could have been due to the very high x'(P. - p)
turbulence induced by having entry at right angles to the
axial flow, in addition to the relatively short filter tube ii) Hindered dispersions
length. Another reason for this effect could have been the In hindered dispersions a force balance can be con-
large amount of fines which were smaller than the structed over a laminar layer of the suspension, instead of
nominal membrane size. Thus a substantial part of the considering individual particles. The centrifugal field
deposit resistance could be due to fine material migrating force is again balanced by the liquid drag force. If there is
into the membrane structure and, therefore, protected no net particle motion and forces due to inertia and
from the shear induced by the crossflow. Visible inspec- gravity can be ignored, then:
tion ofthe filter showed that a deposit cake was formed in
all the filtrations. Crw'(p, - p )Adr - CF oAdr =0 (9)
There is some degree of spread on the experimental where C is the solid volume fraction concentration, F D is
results shown in Figures 10 and II but, nevertheless, it is the drag force per unit volume and A is the area of the
evident that the membrane endcaps did have a consider- laminar layer.
able influence on the filtration behaviour of this material. A liquid force balance results in the following:
If the flux rate was shear rate independent, over this
limited region, then the additional flux given by the dP
dr = CF D (10)
helical or tangential mode of operation must be due to
the centrifugal force field. where dP/dr is the dynamic liquid pressure gradient. This
can be related to solid concentration and velocities by a
Effect of solid concentration and centrifugal acceleration modified form of Darcy's law:
In fluid particle systems the distinction between free dP /l
and hindered systems is usually drawn, based on the solid dr = -1<(1 - C)(v, - v,)
concentration of the dispersion. The threshold between
free and hindered dispersions is often assumed to be where k is the permeability of the layer of solids, v, and v,
approximately 1% by volume, but it is a function of the are the liquid and solid velocities respectively. If the
suspended material. The two concentrations employed in particle layer remains in a stationary orbit, i.e. does not
this study were chosen to be below and above this move towards or foul the membrane, then the solid
threshold, to test the application of centrifugally induced velocity is zero and combining the above equations
anti-fouling of this membrane under both of these oper- provides:
ating conditions. Crw'(p, - p )k
)=v,= /l(1-C) (11)
i) Free dispersions
Equating the liquid drag force with the buoyed centri- Rearranging equation (11) for the centrifugal accelera-
fugal force provides the following equation for radial tion at the membrane surface:
velocity of a particle, if inertia and gravitational body
forces can be neglected and Stokes law is valid: rw' = /l(l - C)J (12)
C(p, - p)k
dr x'(P. - p )rw'
) = dt = 18/l (7) The permeability of a layer of solid§ can be calculated
from various models, one such is Happel and Brenner":
where /l is liquid viscosity, x is particle diameter, dr/dt is
(2 - 3C t /3 + 3C',3 - 2C') x'
the radial velocity of the particle, r is radial position, w is
angular velocity, and P. and p are solid and liquid k= (3 + 2C"') 12C (13)
densities respectively. If the filtrate flux rate is dominated by the resistance to
Equation (7) can be used to estimate the liquid flow flow through the most concentrated laminar layer, which
rate towards the membrane that must be exceeded before is likely to be adjacent to the membrane surface, and this
particles move in the direction of the membrane. At lower layer is assumed to have a porosity of 50% then the
flow rates particles will move outwards, if they are denser permeability of this layer is 1.4 x 10- 13 m 2 by equa-
than the supporting fluid, due to the action of the tion (13).
centrifugal field force. Thus this represents the minimum
flux rate that should be obtained from a membrane
iii) Conservation of angular momentum
incorporating centrifugal separation.
It is extremely difficult to estimate the angular velocity It is possible to estimate the angular velocity and
inside a centrifugal separator in order to apply equa- acceleration at the membrane surface by considering the
tion (7). Conservation of angular momentum is some- geometry of the membrane filter holder, and from a
times used in hydrocyclone investigations, but it is often knowledge of the entry condition. The principle of con-
servation of angular momentum is:
found necessary to introduce empirical coefficients into
the equations. An alternative approach is to estimate the (14)
Table 3. Table of conditions on membrane surface according to models based on free and hindered
dispersions.
..
volume. Helical inserts did, however, lead to additional
W
.,
• " " .
Power (W).
. pressure losses due to fluid drag on the increased surface
area inside the filter module. There is still a considerable
amount of work required to optimise the membrane
~-~-~
holder, and helical insert, in order to enhance the centri-
Figure 12. Equilibrium Dux rates as a function of power requirement fugal field force and shear but to minimise the pressure
for the lS'1o solids suspension. losses in the system.
This anti-fouling technique could also be applied to
suspensions in which the dispersed phase is less dense
'2r--------------------------------------, than the continuous phase, such as oil in water. Under
-:c such circumstances the filtration would have to be ef-
fected on the internal surface of the membrane of circular,
'E
or similar, cross section. The experimental results indi-
"
§. •• cate that the technique is efficient in temis of the energy
d 0 required for separation, with energy savings of 20%
achieved.
NOMENCLATURE
••~----~,,~----~,,~-----~=-------.=.------~~. A
C
Area, m 2
4. Wakeman. R. J. and Tarleton, E. S.. 1991. An experimental study of 12. Happe1. J. and Brenner. H, 1965. Low Reyno/tb nronber hydrody-
electroacoustic crossftow microfiltration, Chem Eng Res Des, 69: namics (Prentice·Hall, Englewood Cliffs. N. 1.).
386.
5. Dcjmek, P., Fuoeles. B., Hallstrom, B. and Winge, L., 1974,
Turbulence promoters in ultrafiltration of whey protein concen-
trate, J Food Science, 39: 1014. ACKNOWLEDGEMENTS
6. Boonthanon, S., Hwan. L. S., Vigneswaran, S., Ben Aim, R. and
The authors of this paper wish to record their gratitude for a Science
Mora, J. C., 1991, Application of pulsatilc cleaning techniques in
and Engineering Research Council grant to support a project of whicb
crossftow microfiltration, Filtration and Separation, 28(3): 199.
tbis work fonned a part.
7. Finnigan. S. M. and Howell, J. A., 1989, The effect ofpulsatilc flow
on ultrafiltration fluxes in a baffied tubular membrane system.
Chem Eng Res Des. 67: 278.
8. Milisic, V. and BersiUon, J. L., 1986, Anti-Coulins techniques in .
crossBow microfiltration, Filtration and Separation. 23(6): 347. ADDRESS
9. Murkes., 1. and Carlsson, C. G., 1988, Crossjiow Filtration (Wiley•. Correspondence concerning this paper should be addressed to Or
Chichester). R. G. Holdich, Department of Chemical Engineering. University of
10. Rusbton, A. and Zbang. G. S.,1988, Rotary microporous filtration. Technology. Loughborough, Leicestershire, LEt 1 3TU.
Desalination. 70: 379.
11. Dave, N. and Gray, N. B., 1989, Modelling of annular swirled flow The manuscripl was received 27 March 1992 and accepled/or publicalion
lances with helical inserts, Tram Inst Mining &: Met, 98: C178. a/ler revision 14 July /992.