FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION
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FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION
FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION
高分子科学(英文版)1989年7卷第2期 页码:150-158
Affiliations:
1. Institute of Chemistry, Academia Sinica,Beijing
2. Academia Sinica
3. Beijing
Author bio:
Funds:
DOI:
中图分类号:
纸质出版:1989-06-20
Accepted:
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[1]钱人元,沈德言,李惠鸣.FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION[J].Chinese Journal of Polymer Science,1989,{4}(02):150-158.
QIAN Renyuan, SHEN Deyan, LI Huiming. FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION[J]. 1989, 7(2): 150-158.
[1]钱人元,沈德言,李惠鸣.FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION[J].Chinese Journal of Polymer Science,1989,{4}(02):150-158.DOI:
QIAN Renyuan, SHEN Deyan, LI Huiming. FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION[J]. 1989, 7(2): 150-158.DOI:
FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION
Three specimens from a solution-cast poly (ethylene terephthalate) (PET) film
one being liquid-N
2
quenched from 92℃(Q)
one being slowly cooled from 92℃(SC) and one being quenched and sub-T
g
annealed at 67℃(AN)
have been studied by specimen difference spectra Q-SC and AN-Q and temperature difference spectra T-70 and T
2
-T
1
for every 2℃steps on heating to 90℃at 2℃/min. SC and AN showed more gauche conformers than Q. That means that the PET chain has more trans conformers at higher temperatures and some of these are frozen during quenching through T
g
. A band at 1340 cm
-1
has been found to be complex containing overlapping bands reflecting trans in crystalline regions and trans in amorphous regions. The temperature difference spectra on heating through T
g
showed that the spectral changes in Q are gradual while a rather abrupt change occurs in AN at 80—82℃for the bands at 1340
1042 and 1020 cm
-1
. No new conformational structure or new vibrational mode is involved. A kind of locking mechanism is suggested which hinders the molecular vibrational changes in AN below T
g
until a sudden release occurs at T
g
. These locking sites can be nothing else than sites of tighter local packing of chain segments. Consequently it is believed that inter-chain van der Waals attraction energy plays a dominating role in the volume relaxation and sub-T
g
annealing of quenched amorphous polymers.
Abstract
Three specimens from a solution-cast poly (ethylene terephthalate) (PET) film
one being liquid-N
2
quenched from 92℃(Q)
one being slowly cooled from 92℃(SC) and one being quenched and sub-T
g
annealed at 67℃(AN)
have been studied by specimen difference spectra Q-SC and AN-Q and temperature difference spectra T-70 and T
2
-T
1
for every 2℃ steps on heating to 90℃ at 2℃ /min. SC and AN showed more gauche conformers than Q. That means that the PET chain has more trans conformers at higher temperatures and some of these are frozen during quenching through T
g
. A band at 1340 cm
-1
has been found to be complex containing overlapping bands reflecting trans in crystalline regions and trans in amorphous regions. The temperature difference spectra on heating through T
g
showed that the spectral changes in Q are gradual while a rather abrupt change occurs in AN at 80—82℃ for the bands at 1340
1042 and 1020 cm
-1
. No new conformational structure or new vibrational mode is involved. A kind of locking mechanism is suggested which hinders the molecular vibrational changes in AN below T
g
until a sudden release occurs at T
g
. These locking sites can be nothing else than sites of tighter local packing of chain segments. Consequently it is believed that inter-chain van der Waals attraction energy plays a dominating role in the volume relaxation and sub-T
g
annealing of quenched amorphous polymers.
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