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Novel Strategy to fabricate Antiwrinkle Cotton fabrics with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature
[Image: see text] As a most promising formaldehyde-free crosslinking agent for the antiwrinkle treatment of cotton fabrics, 1,2,3,4-butanetetracarboxylic acid (BTCA) has been explored for many years to replace the traditional N-methylol resin. However, the current methodology for preparing antiwrink...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434746/ https://www.ncbi.nlm.nih.gov/pubmed/36061653 http://dx.doi.org/10.1021/acsomega.2c03131 |
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author | Hu, Hanchang Dong, Xia Zhao, Qiangqiang Wu, Rongliang Meng, Chen Xu, Jiani Cai, Tingwei Wang, Xin He, Jinxin |
author_facet | Hu, Hanchang Dong, Xia Zhao, Qiangqiang Wu, Rongliang Meng, Chen Xu, Jiani Cai, Tingwei Wang, Xin He, Jinxin |
author_sort | Hu, Hanchang |
collection | PubMed |
description | [Image: see text] As a most promising formaldehyde-free crosslinking agent for the antiwrinkle treatment of cotton fabrics, 1,2,3,4-butanetetracarboxylic acid (BTCA) has been explored for many years to replace the traditional N-methylol resin. However, the current methodology for preparing antiwrinkle cotton fabrics with BTCA mainly highlights the troublesome problem of higher curing temperature. In this research, a novel strategy with the aid of dimethyl sulfone (MSM) was developed to decrease the curing temperature of BTCA for fabricating antiwrinkle cotton fabrics, which is an eco-friendly additive with low price and wonderful biocompatibility. Temperature-dependent Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and computational simulations were employed to analyze the mechanism of MSM in the overall reaction between BTCA and cellulose. Based on the strong hydrogen-bond acceptor property of MSM, the noncovalent interactions in the crosslinking system could be easily interrupted, which facilitates the BTCA diffusion in amorphous regions of cellulose, anhydride formation, and the thermal vibration of cellulose chains during the processing. Physically and chemically speaking, both reactivities of grafting and crosslinking reactions of BTCA are significantly increased with the assistance of MSM, consequently reducing the curing temperature, which will hopefully help achieve the industrial-scale application of BTCA in antiwrinkle treatment. |
format | Online Article Text |
id | pubmed-9434746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94347462022-09-02 Novel Strategy to fabricate Antiwrinkle Cotton fabrics with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature Hu, Hanchang Dong, Xia Zhao, Qiangqiang Wu, Rongliang Meng, Chen Xu, Jiani Cai, Tingwei Wang, Xin He, Jinxin ACS Omega [Image: see text] As a most promising formaldehyde-free crosslinking agent for the antiwrinkle treatment of cotton fabrics, 1,2,3,4-butanetetracarboxylic acid (BTCA) has been explored for many years to replace the traditional N-methylol resin. However, the current methodology for preparing antiwrinkle cotton fabrics with BTCA mainly highlights the troublesome problem of higher curing temperature. In this research, a novel strategy with the aid of dimethyl sulfone (MSM) was developed to decrease the curing temperature of BTCA for fabricating antiwrinkle cotton fabrics, which is an eco-friendly additive with low price and wonderful biocompatibility. Temperature-dependent Fourier-transform infrared spectroscopy, X-ray photoelectron spectroscopy, and computational simulations were employed to analyze the mechanism of MSM in the overall reaction between BTCA and cellulose. Based on the strong hydrogen-bond acceptor property of MSM, the noncovalent interactions in the crosslinking system could be easily interrupted, which facilitates the BTCA diffusion in amorphous regions of cellulose, anhydride formation, and the thermal vibration of cellulose chains during the processing. Physically and chemically speaking, both reactivities of grafting and crosslinking reactions of BTCA are significantly increased with the assistance of MSM, consequently reducing the curing temperature, which will hopefully help achieve the industrial-scale application of BTCA in antiwrinkle treatment. American Chemical Society 2022-08-22 /pmc/articles/PMC9434746/ /pubmed/36061653 http://dx.doi.org/10.1021/acsomega.2c03131 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Hu, Hanchang Dong, Xia Zhao, Qiangqiang Wu, Rongliang Meng, Chen Xu, Jiani Cai, Tingwei Wang, Xin He, Jinxin Novel Strategy to fabricate Antiwrinkle Cotton fabrics with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature |
title | Novel Strategy
to fabricate Antiwrinkle Cotton fabrics
with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature |
title_full | Novel Strategy
to fabricate Antiwrinkle Cotton fabrics
with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature |
title_fullStr | Novel Strategy
to fabricate Antiwrinkle Cotton fabrics
with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature |
title_full_unstemmed | Novel Strategy
to fabricate Antiwrinkle Cotton fabrics
with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature |
title_short | Novel Strategy
to fabricate Antiwrinkle Cotton fabrics
with 1,2,3,4-Butanetetracarboxylic Acid under a Low Temperature |
title_sort | novel strategy
to fabricate antiwrinkle cotton fabrics
with 1,2,3,4-butanetetracarboxylic acid under a low temperature |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434746/ https://www.ncbi.nlm.nih.gov/pubmed/36061653 http://dx.doi.org/10.1021/acsomega.2c03131 |
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