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Addition Polymerisation

1. Addition polymerization is the process of forming long chain polymer molecules from repeating units of monomers. 2. During addition polymerization, the double bond between carbons in a monomer breaks open to form a single carbon bond, linking monomers together into long chains. 3. Common examples of addition polymerization include turning ethene monomers into polyethene, propane monomers into poly(propane), and vinyl chloride monomers into polyvinyl chloride.

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0% found this document useful (0 votes)
49 views3 pages

Addition Polymerisation

1. Addition polymerization is the process of forming long chain polymer molecules from repeating units of monomers. 2. During addition polymerization, the double bond between carbons in a monomer breaks open to form a single carbon bond, linking monomers together into long chains. 3. Common examples of addition polymerization include turning ethene monomers into polyethene, propane monomers into poly(propane), and vinyl chloride monomers into polyvinyl chloride.

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Noura Nawaf
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Addition Polymerisation

of of

Polymer : A
long chain molecule made up repeating units monomer .

Repeat Unit
W ✗

f- f c-]

Wy =D + e-
1 I
n >

{
c-
'
y z f n

Monomer -

any alkene
Polymer

A double bond between the carbon breaks and it opens up


to form the
carbon bond
single .

" ' ' H

f- of
j II
H '
"
I
\c=c / 1
n → c- -
c- c-
/ It, I 1 I 1
H H H h H H
ethene

unit
polylethene) repeating

CH H
H
"
TH3 }

f- if if
H3T / l l
n , = , → e- -
c- c -
'
Y, I
t t
H

propane n µ
repeating unit
Poly ( propane)

at " a H
C'
,H

f. -1oh
I 1
,
d-d
g-

Yo
-

, /
"
I,
I , H H

polyvinyl chloride) repeating unit


vinyl chloride
Cchloroethene)
polylchloroethe.me

or C6

11¥ H
¥ it

t.I-I.tn
"
'
h \c=c →
-
C -
C -

+ ÷ i. a

styrene polylstyrene repeating unit

therefore
-

Polymers are inert and do not


biodegrade .

Why are polymers unreactive ( inert ) ?

they only
-

contain carbon carbon bonds ( saturated )


single
-
.
The
magnitude of '
intermolecular exceed those between
polymers forces can
vastly
small molecules ,

*
f- CH2 -
CH
] f. CHA -
CH >
In
h

permanent dipole dipole Van der Waals


-

-
Van der Waals

Properties of polymers
" '' ¥1
%
,

I" 'I /E - x -- -

Difference material
in
branching on
polymer property

'

Longer chains with fewer branches have stronger intermolecular forces ,


making these
polymer materials

and
stronger more
rigid
.

branches difficult for chains closely form weak


Large make it to
pack together they only

, so

der Waals forces


van
.

:)
CH2 1-1

⇐ of
CH __
I

n

'
I H H
wander Waals forces
strong and
hence strong benzene
in polythene ,
ring is
it
rigid a
large branch , making
difficult for chain -1s to

pack
closely together .

Poly ( chloroethene) ( PVC ) %,

taobao.EE#-PolylchloroetheneJ ,
also known as PVC , is an addition
polymer formed from ehloroethene monomers .

toµ of i
'
" "

n y=f > -

,
H It H di .

?
Why is PVC hard but brittle

Permanent dipole dipole forces formed between chains between the 8- chlorine atoms
are
polymer
-

charge
-

on

the ft atoms
and
charges on carbon .

CI
as -

g-
• µ
THE
jis §
's -
-
Modifying plastics using plasticise.rs

Plastic isers small molecules that


get between the polymer forcing them and
→ are
chains apart
slide
allowing them to across each other .

Plasticisers reduces strength of intermolecular forces between chains ,


making them more flexible .

Recycling of Plastics %
"E -x x x x -

Mechanical
Recycling

Plastics separated into different


types

are
.

→ washed

→ Sorted
→ Ground into pellets

/ [ remoulded
can be
melted

Feedstock
Recycling

Polymer chains heated to


high temperature and chains break down
'

Make new plastics .


7 monomers

Problems

Thermoplastic polymers be softened heated


-

= can when so can be melted + reused .

Some chains break become


may so shorter and properties might change
.

Isotactic :
side ( more desirable properties)
CH3 groups on same

Syndio tactic :
CH3 groups alternate sided

A-tactic Random (most outcome)


likely
:

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