Reorganization of poly(ethylene terephthalate) structures and conformations to alter properties
Reorganization of poly(ethylene terephthalate) structures and conformations to alter properties
复制标题
重组聚对苯二甲酸乙二醇酯结构和构象以改变性能
DOI:
10.1002/polb.21098
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发表时间:
2007
期刊:
影响因子:
--
通讯作者:
A. Tonelli
中科院分区:
文献类型:
--
作者:
Jyotsna Vedula;A. Tonelli
The solid-state morphologies, structures, and chain conformations of poly (ethylene terephthalate) (PET) have been reorganized/altered from those normally produced by solution and melt processing. This has been achieved by two distinct methods: (1) formation of a crystalline inclusion compound (IC) between guest PET and host γ-cylodextrin (γ-CD), followed by removal of the host γ-CD and coalescence of the guest PET (c-PET) and (2) rapid precipitation of PET from a warm trifluoracetic acid solution into a large excess of rapidly stirred acetone (p-PET). Our prior observations (FTIR, NMR, DSC, X-ray) demonstrated that c-PET processed in this manner has a morphology, structure, and non-crystalline chain conformations that are quite distinct from those of as-received PET (asr-PET). Where possible to compare, here we find that c- and p-PETs behave very similarly, but very distinctly from asr-PET. The reorganized c- and p-PETs were found to be repeatedly rapidly crystallizable from the melt with a high level of crystallinity, and in their non-crystalline regions to have tightly packed chains predominantly adopting highly extended kink conformations, which evidence no glass-transition behavior. What is most unusual and somewhat puzzling is that their contrasting structures, morphologies, conformations, and thermal responses were observed to be independent of melt annealing, and persisted even after holding both samples above Tm for extended periods (hours). p-PET, which can be produced in larger quantities than c-PET, was utilized to measure additional macroscopic properties, such as melt viscosities, densities, and the stress-strain and thermal shrinkage of melt-pressed films, for comparison to those of asr-PET. © 2007 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 45: 735–746, 2007
影响因子:
5.5
作者:
H. Choi;T. Ooya;S. Sasaki;N. Yui;Y. Ohya;T. Nakai;T. Ouchi
通讯作者:
H. Choi;T. Ooya;S. Sasaki;N. Yui;Y. Ohya;T. Nakai;T. Ouchi
影响因子:
5.5
作者:
Dong, T;He, Y;Inoue, Y
通讯作者:
Inoue, Y