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Effect of the Trifunctional Chain Extender on Intrinsic Viscosity, Crystallization Behavior, and Mechanical Properties of Poly(Ethylene Terephthalate)
[Image: see text] In this work, poly(ethylene terephthalate) (PET) chain-extending products with different molecular weights were prepared by reactive extrusion using isocyanate trimer (C-HK) as the trifunctional chain extender. The effect of the chain extender C-HK on the intrinsic viscosity, melt...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409260/ https://www.ncbi.nlm.nih.gov/pubmed/32775928 http://dx.doi.org/10.1021/acsomega.0c02815 |
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author | Zhao, Zhiyuan Wu, Yinqiu Wang, Kailun Xia, Yanping Gao, Hongxin Luo, Keming Cao, Zheng Qi, Juan |
author_facet | Zhao, Zhiyuan Wu, Yinqiu Wang, Kailun Xia, Yanping Gao, Hongxin Luo, Keming Cao, Zheng Qi, Juan |
author_sort | Zhao, Zhiyuan |
collection | PubMed |
description | [Image: see text] In this work, poly(ethylene terephthalate) (PET) chain-extending products with different molecular weights were prepared by reactive extrusion using isocyanate trimer (C-HK) as the trifunctional chain extender. The effect of the chain extender C-HK on the intrinsic viscosity, melt flow property, crystallization behavior, crystallization morphology, and mechanical property of PET was investigated. The results showed that when the content of the chain extender was increased from 0.6 to 1.4 wt%, the viscosity average molecular weight of PET was effectively increased from 2.36 × 10(4) to 5.46 × 10(4) g·mol(–1). After the chain extending, the crystallinity and the time of semicrystallization of PET were significantly decreased. After the isothermal crystallization at 220 °C for 5 min, the spherulites formed by pure PET became larger. With the increase in molecular weight of PET after chain extension, its spherulite size was significantly decreased without changing the crystalline structure. The chain-extended PET also exhibited more excellent bending-resistant and impact-resistant properties. While the tensile strength of PET after chain extension was slightly decreased, the bending strength was increased by a maximum value of 56.8%, and the impact strength was increased by a maximum value of five times. |
format | Online Article Text |
id | pubmed-7409260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-74092602020-08-07 Effect of the Trifunctional Chain Extender on Intrinsic Viscosity, Crystallization Behavior, and Mechanical Properties of Poly(Ethylene Terephthalate) Zhao, Zhiyuan Wu, Yinqiu Wang, Kailun Xia, Yanping Gao, Hongxin Luo, Keming Cao, Zheng Qi, Juan ACS Omega [Image: see text] In this work, poly(ethylene terephthalate) (PET) chain-extending products with different molecular weights were prepared by reactive extrusion using isocyanate trimer (C-HK) as the trifunctional chain extender. The effect of the chain extender C-HK on the intrinsic viscosity, melt flow property, crystallization behavior, crystallization morphology, and mechanical property of PET was investigated. The results showed that when the content of the chain extender was increased from 0.6 to 1.4 wt%, the viscosity average molecular weight of PET was effectively increased from 2.36 × 10(4) to 5.46 × 10(4) g·mol(–1). After the chain extending, the crystallinity and the time of semicrystallization of PET were significantly decreased. After the isothermal crystallization at 220 °C for 5 min, the spherulites formed by pure PET became larger. With the increase in molecular weight of PET after chain extension, its spherulite size was significantly decreased without changing the crystalline structure. The chain-extended PET also exhibited more excellent bending-resistant and impact-resistant properties. While the tensile strength of PET after chain extension was slightly decreased, the bending strength was increased by a maximum value of 56.8%, and the impact strength was increased by a maximum value of five times. American Chemical Society 2020-07-24 /pmc/articles/PMC7409260/ /pubmed/32775928 http://dx.doi.org/10.1021/acsomega.0c02815 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Zhao, Zhiyuan Wu, Yinqiu Wang, Kailun Xia, Yanping Gao, Hongxin Luo, Keming Cao, Zheng Qi, Juan Effect of the Trifunctional Chain Extender on Intrinsic Viscosity, Crystallization Behavior, and Mechanical Properties of Poly(Ethylene Terephthalate) |
title | Effect of the Trifunctional Chain Extender on Intrinsic
Viscosity, Crystallization Behavior, and Mechanical Properties of
Poly(Ethylene Terephthalate) |
title_full | Effect of the Trifunctional Chain Extender on Intrinsic
Viscosity, Crystallization Behavior, and Mechanical Properties of
Poly(Ethylene Terephthalate) |
title_fullStr | Effect of the Trifunctional Chain Extender on Intrinsic
Viscosity, Crystallization Behavior, and Mechanical Properties of
Poly(Ethylene Terephthalate) |
title_full_unstemmed | Effect of the Trifunctional Chain Extender on Intrinsic
Viscosity, Crystallization Behavior, and Mechanical Properties of
Poly(Ethylene Terephthalate) |
title_short | Effect of the Trifunctional Chain Extender on Intrinsic
Viscosity, Crystallization Behavior, and Mechanical Properties of
Poly(Ethylene Terephthalate) |
title_sort | effect of the trifunctional chain extender on intrinsic
viscosity, crystallization behavior, and mechanical properties of
poly(ethylene terephthalate) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7409260/ https://www.ncbi.nlm.nih.gov/pubmed/32775928 http://dx.doi.org/10.1021/acsomega.0c02815 |
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