CH 04
CH 04
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CHAPTER 4
POLYMER STRUCTURES
PROBLEM SOLUTIONS
Hydrocarbon Molecules
Polymer Molecules
The Chemistry of Polymer Molecules
Molecular Weight
4.2 Mer weights for several polymers are asked for in this problem.
(a) For polytetrafluoroethylene, each mer unit consists of two carbons and four fluorines (Table 4.3). If
AC and AF represent the atomic weights of carbon and fluorine, respectively, then
m = 2(AC) + 4(AF)
(b) For poly(methyl methacrylate), from Table 4.3, each mer unit has five carbons, eight hydrogens, and
two oxygens. Thus,
(c) For nylon 6,6, from Table 4.3, each mer unit has twelve carbons, twenty-two hydrogens, two nitrogens,
and two oxygens. Thus,
= 226.32 g/mol
(d) For poly(ethylene terephthalate), from Table 4.3, each mer unit has ten carbons, eight hydrogens, and
four oxygens. Thus,
4.3 We are asked to compute the number-average degree of polymerization for polypropylene, given that
the number-average molecular weight is 1,000,000 g/mol. The mer molecular weight of polypropylene is just
m = 3(AC) + 6(AH)
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If we let nn represent the number-average degree of polymerization, then from Equation 4.4a
Mn 106 g/mol
nn = = = 23, 700
m 42.08 g/mol
4.4 (a) The mer molecular weight of polystyrene is called for in this portion of the problem. For
polystyrene, from Table 4.3, each mer unit has eight carbons and eight hydrogens. Thus,
m = 8(AC) + 8(AH)
(b) We are now asked to compute the weight-average molecular weight. Since the weight-average degree
of polymerization, nw, is 25,000, using Equation 4.4b
4.5 (a) From the tabulated data, we are asked to compute M n , the number-average molecular weight.
Molecular wt
Range Mean Mi xi xiMi
(b) From the tabulated data, we are asked to compute M w , the weight-average molecular weight.
Molecular wt.
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Range Mean Mi wi wiMi
(c) Now we are asked to compute nn (the number-average degree of polymerization), using Equation 4.4a.
For polypropylene,
m = 3(AC) + 6(AH)
And
Mn 33, 040 g/mol
nn = = = 785
m 42.08 g/mol
(d) And, finally, we are asked to compute nw, the weight-average degree of polymerization, as
4.6 (a) From the tabulated data, we are asked to compute M n , the number-average molecular weight.
Molecular wt.
Range Mean Mi xi xi M i
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68,000-80,000 74,000 0.10 7400
80,000-92,000 86,000 0.03 2580
_________________________
M n = ∑ x i M i = 47, 720 g/mol
(b) From the tabulated data, we are asked to compute M w , the weight-average molecular weight. This
Molecular wt.
Range Mean Mi wi wiMi
(c) We are now asked if the number-average degree of polymerization is 477, which of the polymers in
Table 4.3 is this material? It is necessary to compute m in Equation 4.4a as
The mer molecular weights of the polymers listed in Table 4.3 are as follows:
Polyethylene--28.05 g/mol
Poly(vinyl chloride)--62.49 g/mol
Polytetrafluoroethylene--100.02 g/mol
Polypropylene--42.08 g/mol
Polystyrene--104.14 g/mol
Poly(methyl methacrylate)--100.11 g/mol
Phenol-formaldehyde--133.16 g/mol
Nylon 6,6--226.32 g/mol
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PET--192.16 g/mol
Polycarbonate--254.27 g/mol
Therefore, polytetrafluoroethylene is the material since its mer molecular weight is closest to that calculated above.
(d) The weight-average degree of polymerization may be calculated using Equation 4.4b, since M w and
4.7 This problem asks if it is possible to have a poly(vinyl chloride) homopolymer with the given
molecular weight data and a number-average degree of polymerization of 1120. The appropriate data are given
below along with a computation of the number-average molecular weight.
Molecular wt.
Range Mean Mi xi xi M i
For PVC, from Table 4.3, each mer unit has two carbons, three hydrogens, and one chlorine. Thus,
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Thus, such a homopolymer is not possible since the calculated nn is 764 not 1120.
4.8 (a) For chlorinated polyethylene, we are asked to determine the weight percent of chlorine added for
5% Cl substitution of all original hydrogen atoms. Consider 50 carbon atoms; there are 100 possible side-bonding
sites. Ninety-five are occupied by hydrogen and five are occupied by Cl. Thus, the mass of these 50 carbon atoms,
mC, is just
177.25 g
CCl = x 100 = 20.3 wt%
600.5 g + 95.76 g + 177.25 g
(b) Chlorinated polyethylene differs from poly(vinyl chloride), in that, for PVC, (1) 25% of the side-
bonding sites are substituted with Cl, and (2) the substitution is probably much less random.
Molecular Shape
4.9 This problem first of all asks for us to calculate, using Equation 4.7, the average total chain length, L,
for a linear polyethylene polymer having a number-average molecular weight of 300,000 g/mol. It is necessary to
calculate the number-average degree of polymerization, nn, using Equation 4.4a. For polyethylene, from Table 4.3,
each mer unit has two carbons and four hydrogens. Thus,
m = 2(AC) + 4(AH)
and
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Mn 300, 000 g/mol
nn = = = 10, 695
m 28.05 g/mol
which is the number of mer units along an average chain. Since there are two carbon atoms per mer unit, there are
two C--C chain bonds per mer, which means that the total number of chain bonds in the molecule, N, is just
(2)(10,695) = 21,390 bonds. Furthermore, assume that for single carbon-carbon bonds, d = 0.154 nm and θ = 109°
(Section 4.4); therefore, from Equation 4.7
⎛θ ⎞
L = Nd sin ⎜ ⎟
⎝ 2⎠
⎡ ⎛ 109° ⎞ ⎤
= (21, 390)(0.154 nm) ⎢sin ⎜ ⎟ ⎥ = 2682 nm
⎣ ⎝ 2 ⎠⎦
It is now possible to calculate the average chain end-to-end distance, r, using Equation 4.8 as
4.10 (a) This portion of the problem asks for us to calculate the number-average molecular weight for a
linear polytetrafluoroethylene for which L in Equation 4.7 is 2000 nm. It is first necessary to compute the value of
N using this equation, where, for the C--C chain bond, d = 0.154 nm, and θ = 109°. Thus
L
N =
⎛ θ⎞
d sin ⎜ ⎟
⎝ 2⎠
2000 nm
= = 15, 900
⎛ 109°⎞
(0.154 nm) sin ⎜ ⎟
⎝ 2 ⎠
Since there are two C--C bonds per PTFE mer unit, there is an average of N/2 or 15,900/2 = 7950 mer units per
chain, which is also the number-average degree of polymerization, nn. In order to compute the value of M n using
Equation 4.4a, we must first determine m for PTFE. Each PTFE mer unit consists of two carbon and four fluorine
atoms, thus
m = 2(AC) + 4(AF)
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= (2)(12.01 g/mol) + (4)(19.00 g/mol) = 100.02 g/mol
Therefore
M n = nn m = (7950)(100.02 g/mol) = 795, 000 g/mol
(b) Next, we are to determine the number-average molecular weight for r = 15 nm. Solving for N from
Equation 4.8 leads to
r2 (15 nm) 2
N = = = 9490
d2 (0.154 nm) 2
which is the total number of bonds per average molecule. Since there are two C--C bonds per mer unit, then nn =
Molecular Configurations
4.11 We are asked to sketch portions of a linear polypropylene molecule for different configurations
(using two-dimensional schematic sketches).
(a) Syndiotactic polypropylene
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(c) Isotactic polypropylene
4.12 This problem asks for us to sketch cis and trans structures for butadiene and chloroprene.
(a) The structure for cis polybutadiene is
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Thermoplastic and Thermosetting Polymers
4.13 This question asks for comparisons of thermoplastic and thermosetting polymers.
(a) Thermoplastic polymers soften when heated and harden when cooled, whereas thermosetting polymers,
harden upon heating, while further heating will not lead to softening.
(b) Thermoplastic polymers have linear and branched structures, while for thermosetting polymers, the
structures will normally be network or crosslinked.
4.14 (a) It is not possible to grind up and reuse phenol-formaldehyde because it is a network thermoset
polymer and, therefore, is not amenable to remolding.
(b) Yes, it is possible to grind up and reuse polypropylene since it is a thermoplastic polymer, will soften
when reheated, and, thus, may be remolded.
Copolymers
4.15 This problem asks for sketches of the mer structures for several alternating copolymers.
(a) For poly(ethylene-propylene)
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(c) For poly(isobutylene-isoprene)
m = 12(AC) + 14(AH)
4.17 This problem asks for us to calculate the number-average molecular weight of a random nitrile
[poly(acrylonitrile-butadiene) copolymer]. For the acrylonitrile mer there are three carbon, one nitrogen, and three
hydrogen atoms. Thus, its mer molecular weight is
The butadiene mer is composed of four carbon and six hydrogen atoms. Thus, its mer molecular weight is
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= (4)(12.01 g/mol) + (6)(1.008 g/mol) = 54.09 g/mol
Since nn = 2000 (as stated in the problem), M n may be computed using Equation 4.4a as
4.18 For an alternating copolymer that has a number-average molecular weight of 100,000 g/mol and a
number-average degree of polymerization of 2210, we are to determine one of the mer types if the other type is
ethylene. It is first necessary to calculate m using Equation 4.4a as
Since this is an alternating copolymer we know that chain fraction of each mer type is 0.5; that is fe = fx = 0.5, fe
and fx being, respectively, the chain fractions of the ethylene and unknown mers. Also, the mer molecular weight
for ethylene is
ms = 2(AC) + 4(AH)
Now, using Equation 4.5, it is possible to calculate the mer weight of the unknown mer type, mx. Thus
m − feme
mx =
fx
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Finally, it is necessary to calculate the mer molecular weights for each of the possible other mer types.
These are calculated below:
Therefore, vinyl chloride is the other mer type since its m value is almost the same as the calculated mx.
4.19 (a) This portion of the problem asks us to determine the ratio of butadiene to acrylonitrile mers in a
copolymer having a weight-average molecular weight of 250,000 g/mol and a weight-average degree of
polymerization of 4640. It first becomes necessary to calculate the average mer molecular weight of the copolymer,
m , using Equation 4.4b as
If we designate fb as the chain fraction of butadiene mers, since the copolymer consists of only two mer types, the
chain fraction of acrylontrile mers fa is just 1 – fb. Now, Equation 4.5 for this copolymer may be written in the form
m = f b mb + fa ma = f b mb + (1 − f b ) ma
in which mb and ma are the mer molecular weights for butadiene and acrylontrile, respectively. These values are
calculated as follows:
= 53.06 g/mol.
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Furthermore, fa = 1 – fb = 1 – 0.80 = 0.20; or the ratio is just
fb 0.80
= = 4.0
fa 0.20
(b) Of the possible copolymers, the only one for which there is a restriction on the ratio of mer types is
alternating; the ratio must be 1:1. Therefore, on the basis of the result in part (a), the possibilities for this
copolymer are random, graft, and block.
4.20 For a copolymer consisting of 60 wt% ethylene and 40 wt% propylene, we are asked to determine the
fraction of both mer types.
In 100 g of this material, there are 60 g of ethylene and 40 g of propylene. The ethylene (C2H4) molecular
weight is
60 g
= 2.14 mol of ethylene
28.05 g / mol
and
40 g
= 0.95 mol of propylene
42.08 g / mol
2.14 mol
f (ethylene) = = 0.69
2.14 mol + 0.95 mol
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Likewise,
0.95 mol
f (propylene) = = 0.31
2.14 mol + 0.95 mol
4.21 For a random poly(isobutylene-isoprene) copolymer in which M w = 200,000 g/mol and nw = 3000,
Also, from Table 4.5, the isoprene mer has five carbon and eight hydrogen atoms, and
m = fibmib + fipmip
m = 56.10x + (68.11)(1 − x)
Mw
nw =
m
Or
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Polymer Crystallinity
4.22 The tendency of a polymer to crystallize decreases with increasing molecular weight because as the
chains become longer it is more difficult for all regions along adjacent chains to align so as to produce the ordered
atomic array.
4.23 For each of four pairs of polymers, we are asked to (1) state whether it is possible to decide which is
more likely to crystallize; (2) if so, which is more likely and why; and (3) it is not possible to decide then why.
(a) No, it is not possible to decide for these two polymers. On the basis of tacticity, the isotactic PP is more
likely to crystallize than the atactic PVC. On the other hand, with regard to side-group bulkiness, the PVC is more
likely to crystallize.
(b) Yes, it is possible to decide for these two copolymers. The linear and syndiotactic polypropylene is
more likely to crystallize than crosslinked cis-isoprene since linear polymers are more likely to crystallize than
crosslinked ones.
(c) Yes, it is possible to decide for these two polymers. The linear and isotactic polystyrene is more likely
to crystallize than network phenol-formaldehyde; network polymers rarely crystallize, whereas isotactic ones
crystallize relatively easily.
(d) Yes, it is possible to decide for these two copolymers. The block poly(acrylonitrile-isoprene)
copolymer is more likely to crystallize than the graft poly(chloroprene-isobutylene) copolymer. Block copolymers
crystallize more easily than graft ones.
4.24 Given that polyethylene has an orthorhombic unit cell with two equivalent mer units, we are asked to
compute the density of totally crystalline polyethylene. In order to solve this problem it is necessary to employ
Equation 3.5, in which n represents the number of mer units within the unit cell (n = 2), and A is the mer molecular
weight, which for polyethylene is
A = 2(AC) + 4(AH)
Also, VC is the unit cell volume, which is just the product of the three unit cell edge lengths in Figure 4.10. Thus,
nA
ρ =
V N
C A
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(2 mers/uc)(28.05 g/mol)
=
( 7.41 x 10 -8 cm)( 4.94 x 10 -8 cm)( 2.55 x 10-8 cm)/(unit cell)( 6.023 x 10 23 mers/mol)
= 0.998 g/cm3
4.25 For this problem we are given the density of nylon 6,6 (1.213 g/cm3), an expression for the volume
of its unit cell, and the lattice parameters, and are asked to determine the number of mer units per unit cell. This
computation necessitates the use of Equation 3.5, in which we solve for n. Before this can be carried out we must
first calculate VC, the unit cell volume, and A the mer molecular weight. For VC
The mer unit for nylon 6,6 is shown in Table 4.3, from which the value of A may be determined as follows:
= 226.32 g/mol
ρVC N A
n =
A
= 1 mer/unit cell
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4.26 (a) We are asked to compute the densities of totally crystalline and totally amorphous polyethylene
% crystallinity
(ρc and ρa from Equation 4.6). From Equation 4.6 let C = , such that
100
ρ c (ρ s − ρ a )
C =
ρ s (ρ c − ρ a )
ρ c (C ρ s − ρ s ) + ρc ρ a − C ρ s ρ a = 0
in which ρc and ρa are the variables for which solutions are to be found. Since two values of ρs and C are specified
ρ c (C1 ρ s1 − ρ s1 ) + ρ c ρa − C1 ρ s1 ρ a = 0
ρ c (C 2 ρ s2 − ρ s2 ) + ρ c ρa − C 2 ρ s2 ρ a = 0
In which ρs1 = 0.965 g/cm3, ρs2 = 0.925 g/cm3, C1 = 0.768, and C2 = 0.464. Solving the above two equations for
ρa and ρc leads to
ρ s1 ρs2 (C1 − C 2 )
ρa =
C ρ − C ρ
1 s1 2 s2
And
ρ s1 ρ s2 (C 2 − C1 )
ρc =
ρ s2 (C2 − 1 ) − ρ s1 (C1 − 1)
(b) Now we are to determine the % crystallinity for ρs = 0.950 g/cm3. Again, using Equation 4.6
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ρ c (ρ s − ρ a )
% crystallinity = x 100
ρ s (ρ c − ρ a )
= 65.7%
4.27 (a) We are asked to compute the densities of totally crystalline and totally amorphous polypropylene
% crystallinity
(ρc and ρa from Equation 4.6). From Equation 4.6 let C = , such that
100
ρ c (ρ s − ρ a )
C =
ρ s (ρ c − ρ a )
ρ c (C ρ s − ρ s ) + ρ cρ a − C ρ sρ a = 0
in which ρc and ρa are the variables for which solutions are to be found. Since two values of ρs and C are specified
ρ c (C1 ρ s1 − ρ s1 ) + ρ cρ a − C1 ρ s1 ρ a = 0
ρ c (C 2 ρ s 2 − ρ s2 ) + ρ cρ a − C 2 ρ s2 ρ a = 0
In which ρs1 = 0.904 g/cm3, ρs2 = 0.895 g/cm3, C1 = 0.628, and C2 = 0.544. Solving the above two equations for
ρa and ρc leads to
ρ s1 ρ s2 (C1 − C 2 )
ρa =
C1 ρ s1 − C 2 ρ s2
And
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ρ s1 ρ s2 (C 2 − C1 )
ρc =
ρ (C2 − 1) − ρ (C1 − 1)
s2 s1
(b) Now we are asked to determine the density of a specimen having 74.6% crystallinity. Solving for ρs
from Equation 4.6 and substitution for ρa and ρc which were computed in part (a) yields
− ρc ρ a
ρs =
C (ρ c − ρ a ) − ρ c
− ( 0.946 g / cm 3 )( 0.841 g / cm 3 )
=
( 0.746) (0.946 g / cm 3 − 0.841 g / cm 3 ) − 0.946 g / cm 3
= 0.917 g/cm3
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