Chemistry Reference
In-Depth Information
Table 4.2
Glass Transition and Crystal Melting Temperatures of Polymers ( C)
T m a
T m a
T g
T g
Poly(dimethyl siloxane)
2
127
Poly(ethyl methacrylate)
65
120 b
Polyethylene
2
140
Poly(propyl
methacrylate)
35
Polypropylene(isotactic)
2
8
176
Poly(n-butyl
methacrylate)
21
Poly(1-butene) (isotactic)
2
24
132
Poly(n-hexyl
methacrylate)
2
5
Polyisobutene
2
73
Poly(phenyl
methacrylate)
110
Poly(4-methyl-1-penetene)
(isotactic)
29
250
Poly(acrylic acid)
106
cis-1,4-Polybutadiene
2
102
Polyacrylonitrile
97
58 b
96 b
trans-1,4-Polybutadiene
2
Poly(vinyl chloride)
87
(conventional)
cis-1,4-Polyisoprene
273
Poly(vinyl fluoride)
41
200
282 b
Polyformaldehyde
175
Poly(vinylidene chloride)
218
200
Polystyrene (atactic)
100
Poly(vinyl acetate)
32
Poly(alpha-methyl styrene)
168
Poly(vinyl alcohol)
85
Poly(methyl acrylate)
10
Polycarbonate of
bisphenol A
157
Poly(ethyl acrylate)
2
24
Poly(ethylene
terephthalate)
69
267
(unoriented)
50 b
Poly(propyl acrylate)
2
37
Nylon-6,6 (unoriented)
265
Poly(phenyl acrylate)
57
Poly(p-xylene)
375
Poly(methyl methacrylate)
(atactic)
105
a T m is not listed for vinyl polymers in which the most common forms are attactic nor for elastomers,
which are not crystalline in the unstretched state.
b Conflicting data are reported.
The kinetic flexibility of a macromolecule is directly related to the ease with
which conformational changes between trans and gauche states can take place.
The lower the energy barrier
E in Fig. 1.6, the greater the ease of rotation about
main chain bonds. Polymers with low chain stiffnesses will have low T g 's in the
absence of complications from interchain forces. Chain backbones with
Δ
Si
O
or
C
O
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