Chemistry Reference
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Figure 8.20 Dynamic mechanical analysis results. (a) Storage modulus and
(b) damping parameter for the cured neat UPR and UPR/COPERMA resins.
Storage modulus (E 0 ), glass-transition temperature (T g ), cross-link density
(n e ), and effective molar mass between cross-links (M c ), 10 and 50%
weight-loss temperatures (T 10 and T 50 ), and temperature at the maximum
weight-loss rate (T p ) of neat UPR and UPR/COPERMA resins.
Table 8.5
E 0 at
35 1C/GPa T g /1C
n e /
10 3 mol m 3 M c /
g mol 1
Sample
T 10 /1C T 50 /1C T p /1C
UPR
1.26
80.3
2.27
484
348.5
401.2
403.7
UPR/COPERMA5
1.48
79.4
2.36
466
344.4
399.4
399.2
UPR/COPERMA10 1.32
80.9
2.48
444
343.4
400.6
401.6
UPR/COPERMA15 1.14
83.7
2.57
429
340.4
400.7
401.0
UPR/COPERMA20 1.01
81.6
2.42
454
328.2
401.4
400.2
all the bio-materials were thermally stable in an N 2 atmosphere below
150 1C and exhibited a three-stage thermal-degradation process above this
temperature similar to the above DCPD-UPR-TO resins. Table 8.5 summar-
izes the thermal property data of these bio-based plastics, including T 10 , T 50 ,
and the temperature at maximum weight-loss rate (T p ). As the content of
COPERMA resin increased, T 10 decreased while T 50 and T p almost remained
unchanged. The decrease of T 10 can be mainly attributed to the de-
composition of the COPERMA, the co-polymer of which was cured using the
method in Can et al. 24 and showed a T 10 value of 279.8 1C (its TGA curve
is not included in this chapter). However, the T 10 decrease was slight when
0-15 wt% of the UPR was replaced with the COPERMA resin. Hence, the
prepared bio-based materials demonstrated only slightly inferior thermal
stability compared to the pure UPR matrix.
 
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