2014
DOI: 10.1177/096739111402200406
|View full text |Cite
|
Sign up to set email alerts
|

Nonisothermal Crystallization Behaviour of a Novel Cycloaliphatic Microcrystalline Poly(4,4'-Aminocyclohexyl Methylene Dodecanedicarboxylamide)

Abstract: Nonisothermal melt crystallization behaviour and crystallization kinetics of poly(4,4'-aminocyclohexyl methylene dodecanedicarboxylamide), a novel cycloaliphatic microcrystalline polyamide (named PA PACM12), are investigated by differential scanning calorimetry (DSC). The results show that with decreasing cooling rate, the crystallization peak becomes narrower and shifts to higher temperature, while the crystallization enthalpy increases. The Avrami equation, Ozawa model and Mo method are proved to be suitable… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(1 citation statement)
references
References 31 publications
(33 reference statements)
0
1
0
Order By: Relevance
“…The thermal results of the copolymers are displayed in Figure 3 and Table S1 . As displayed in Figure 4 a, the crystallization peak of the copolymer exhibited a significant reduction in the crystallization temperature compared with the PA66 matrix due to the presence of the rigid cyclic structure in PACM6 that hindered the motions of the polymer chains during the crystallization process, which further affected the crystallization ability of molecular chains as a result [ 39 ]. Moreover, the crystallinity of the synthesized copolymer decreased from 28.3% to 15.6% ( Figure 4 b and Table S1 ), indicating that the crystallizing ability of the copolymer was much lower than that of PA66, which was ascribed to the random polymerization of PA66/PACM6 that reduced the regularity of the molecular chain alignment.…”
Section: Resultsmentioning
confidence: 99%
“…The thermal results of the copolymers are displayed in Figure 3 and Table S1 . As displayed in Figure 4 a, the crystallization peak of the copolymer exhibited a significant reduction in the crystallization temperature compared with the PA66 matrix due to the presence of the rigid cyclic structure in PACM6 that hindered the motions of the polymer chains during the crystallization process, which further affected the crystallization ability of molecular chains as a result [ 39 ]. Moreover, the crystallinity of the synthesized copolymer decreased from 28.3% to 15.6% ( Figure 4 b and Table S1 ), indicating that the crystallizing ability of the copolymer was much lower than that of PA66, which was ascribed to the random polymerization of PA66/PACM6 that reduced the regularity of the molecular chain alignment.…”
Section: Resultsmentioning
confidence: 99%