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Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate)
We conducted a preliminary study on fiber structural development in the high-speed melt spinning of environmentally friendly polyethylene terephthalate (Ti-PET) synthesized with 25 ppm of titanium-based catalyst, which was compared with conventional PET (Sb-PET) synthesized with 260 ppm of antimony-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961032/ https://www.ncbi.nlm.nih.gov/pubmed/31771127 http://dx.doi.org/10.3390/polym11121931 |
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author | Kim, Eun Seon Oh, Hyun Ju Kim, Hyun-Joong Kim, Chun Gi Park, Seong Yoon Jeong, Young Gyu Hahm, Wan-Gyu |
author_facet | Kim, Eun Seon Oh, Hyun Ju Kim, Hyun-Joong Kim, Chun Gi Park, Seong Yoon Jeong, Young Gyu Hahm, Wan-Gyu |
author_sort | Kim, Eun Seon |
collection | PubMed |
description | We conducted a preliminary study on fiber structural development in the high-speed melt spinning of environmentally friendly polyethylene terephthalate (Ti-PET) synthesized with 25 ppm of titanium-based catalyst, which was compared with conventional PET (Sb-PET) synthesized with 260 ppm of antimony-based catalyst. Gel permeation chromatography of Ti- and Sb-PET resins of intrinsic viscosity 0.63 confirmed that both resins have similar molecular weights and distributions. However, differential scanning calorimetry revealed that the Ti-PET resin exhibited a lower melt–crystallization peak and isothermal melt-crystallization rate than the Sb-PET resin. High-speed melt spinning of the Ti- and Sb-PET was possible up to a spinning velocity of 6 km/min. Two-dimensional wide-angle X-ray diffraction analyses showed that the molecular orientation of the obtained as-spun Ti- and Sb-PET fibers increased with spinning velocity, and a highly oriented, crystalline structure by orientation-induced crystallization started to appear from 5 km/min. Notably, Ti-PET fibers showed a lower degree of crystalline structural development and lower tensile strength compared with Sb-PET fibers under the high-speed spinning conditions. Our results suggest that the catalyst in PET resins can act as nucleating agents in thermal- and orientation-induced crystallization, and that differences in catalyst content can influence PET fiber structure development under extreme conditions in high-speed melt spinning. |
format | Online Article Text |
id | pubmed-6961032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-69610322020-01-24 Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) Kim, Eun Seon Oh, Hyun Ju Kim, Hyun-Joong Kim, Chun Gi Park, Seong Yoon Jeong, Young Gyu Hahm, Wan-Gyu Polymers (Basel) Article We conducted a preliminary study on fiber structural development in the high-speed melt spinning of environmentally friendly polyethylene terephthalate (Ti-PET) synthesized with 25 ppm of titanium-based catalyst, which was compared with conventional PET (Sb-PET) synthesized with 260 ppm of antimony-based catalyst. Gel permeation chromatography of Ti- and Sb-PET resins of intrinsic viscosity 0.63 confirmed that both resins have similar molecular weights and distributions. However, differential scanning calorimetry revealed that the Ti-PET resin exhibited a lower melt–crystallization peak and isothermal melt-crystallization rate than the Sb-PET resin. High-speed melt spinning of the Ti- and Sb-PET was possible up to a spinning velocity of 6 km/min. Two-dimensional wide-angle X-ray diffraction analyses showed that the molecular orientation of the obtained as-spun Ti- and Sb-PET fibers increased with spinning velocity, and a highly oriented, crystalline structure by orientation-induced crystallization started to appear from 5 km/min. Notably, Ti-PET fibers showed a lower degree of crystalline structural development and lower tensile strength compared with Sb-PET fibers under the high-speed spinning conditions. Our results suggest that the catalyst in PET resins can act as nucleating agents in thermal- and orientation-induced crystallization, and that differences in catalyst content can influence PET fiber structure development under extreme conditions in high-speed melt spinning. MDPI 2019-11-22 /pmc/articles/PMC6961032/ /pubmed/31771127 http://dx.doi.org/10.3390/polym11121931 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Eun Seon Oh, Hyun Ju Kim, Hyun-Joong Kim, Chun Gi Park, Seong Yoon Jeong, Young Gyu Hahm, Wan-Gyu Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) |
title | Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) |
title_full | Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) |
title_fullStr | Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) |
title_full_unstemmed | Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) |
title_short | Effect of Polycondensation Catalyst on Fiber Structure Development in High-Speed Melt Spinning of Poly (Ethylene Terephthalate) |
title_sort | effect of polycondensation catalyst on fiber structure development in high-speed melt spinning of poly (ethylene terephthalate) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6961032/ https://www.ncbi.nlm.nih.gov/pubmed/31771127 http://dx.doi.org/10.3390/polym11121931 |
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