1987
DOI: 10.1016/0032-3861(87)90441-1
|View full text |Cite
|
Sign up to set email alerts
|

CO2-induced crystallization of poly(ethylene terephthalate)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

2
86
0
2

Year Published

1997
1997
2021
2021

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 113 publications
(90 citation statements)
references
References 22 publications
2
86
0
2
Order By: Relevance
“…Further, it can induce crystallization of the matrix and cause an increase in the melting temperature and melting enthalpy. [23][24][25][26] Here, differential scanning calorimetry measurement was performed to study the crystallinity of virgin and foamed PLA/starch composites. The experimental results are shown in Figure 4.…”
Section: Crystallinity Of the Foaming Materialsmentioning
confidence: 99%
“…Further, it can induce crystallization of the matrix and cause an increase in the melting temperature and melting enthalpy. [23][24][25][26] Here, differential scanning calorimetry measurement was performed to study the crystallinity of virgin and foamed PLA/starch composites. The experimental results are shown in Figure 4.…”
Section: Crystallinity Of the Foaming Materialsmentioning
confidence: 99%
“…Sufficient relaxation in polymers caused either by heating or dissolution of CO 2 can result in an increase of free volume and hence chain ordering and crystallization in the polymers. CO 2 -induced crystallization has been observed in poly(ethylene terephthalate) (PET), 6 poly(pphenylene sulfide), 7 polycarbonate, 8 poly(ether ether ketone), 9 methyl-substituted poly(ether ether ketone) 10 and poly(lactic acid) (PLA). 11 Under a CO 2 environment, the crystalline melt point (T m ) and cold crystallization temperature (T c ) are also depressed.…”
Section: Introductionmentioning
confidence: 99%
“…[28][29][30][31] Consequently, a polymer can crystallize at a temperature below its nominal T g when contacted with supercritical fluids. [32][33][34][35][36][37][38] Unlike liquid solvents and vapors, the activity of a supercritical fluid can be changed continuously by simply changing its pressure. Furthermore, fluids like CO 2 are easily removed from the polymer matrix by depressurizing the system, thus making them better candidates to change the polymer morphology.…”
Section: Introductionmentioning
confidence: 99%