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Melt spinnabilities of thermoplastic paramylon mixed esters
The low thermoplasticities of polysaccharide esters make them unsuitable for melt spinning. In this study, we aimed to overcome this problem by mixed esterification of paramylon, a euglenoid β-1,3-glucan with short- and medium-chain acyl groups, as melt-spinnable materials. Thermal analyses revealed...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895648/ https://www.ncbi.nlm.nih.gov/pubmed/31844742 http://dx.doi.org/10.1016/j.heliyon.2019.e02843 |
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author | Shibakami, Motonari Sohma, Mitsugu Kijima, Norihito Nemoto, Tadashi |
author_facet | Shibakami, Motonari Sohma, Mitsugu Kijima, Norihito Nemoto, Tadashi |
author_sort | Shibakami, Motonari |
collection | PubMed |
description | The low thermoplasticities of polysaccharide esters make them unsuitable for melt spinning. In this study, we aimed to overcome this problem by mixed esterification of paramylon, a euglenoid β-1,3-glucan with short- and medium-chain acyl groups, as melt-spinnable materials. Thermal analyses revealed that all the synthesized paramylon mixed esters exhibited glass transition temperatures greater than 100 °C; some of them showed large differences between the melting and 5%-weight-loss temperatures (Td5s) and are extrudable through a spinneret at a temperature ~100 °C below Td5, rendering them potential candidates for the production of melt-spun filaments. Among the various compounds investigated, paramylon acetate propionates, in which the degrees of acetyl- and propionyl-group substitution were 0.5–0.7 and 2.2–2.5, respectively, could be melt-spun to yield mechanically tough crystalline monofilaments. In contrast, the melt spinning of cellulose acetate propionate, analogous to the paramylon acetate propionates in terms of acyl substituents, their substitution degrees, and molecular weights, but differs from it in terms of the glucose linkage mode (i.e., β-1,3 vs β-1,4), yielded brittle, charred, and short filaments. Curdlan acetate propionate, another analogue with a degree of polymerization five times larger than that of paramylon mixed esters, was not extrudable due to the lack of thermoplasticity. Therefore, we herein confirmed the superiority of paramylon as a primary raw material for melt-spun filaments. |
format | Online Article Text |
id | pubmed-6895648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-68956482019-12-16 Melt spinnabilities of thermoplastic paramylon mixed esters Shibakami, Motonari Sohma, Mitsugu Kijima, Norihito Nemoto, Tadashi Heliyon Article The low thermoplasticities of polysaccharide esters make them unsuitable for melt spinning. In this study, we aimed to overcome this problem by mixed esterification of paramylon, a euglenoid β-1,3-glucan with short- and medium-chain acyl groups, as melt-spinnable materials. Thermal analyses revealed that all the synthesized paramylon mixed esters exhibited glass transition temperatures greater than 100 °C; some of them showed large differences between the melting and 5%-weight-loss temperatures (Td5s) and are extrudable through a spinneret at a temperature ~100 °C below Td5, rendering them potential candidates for the production of melt-spun filaments. Among the various compounds investigated, paramylon acetate propionates, in which the degrees of acetyl- and propionyl-group substitution were 0.5–0.7 and 2.2–2.5, respectively, could be melt-spun to yield mechanically tough crystalline monofilaments. In contrast, the melt spinning of cellulose acetate propionate, analogous to the paramylon acetate propionates in terms of acyl substituents, their substitution degrees, and molecular weights, but differs from it in terms of the glucose linkage mode (i.e., β-1,3 vs β-1,4), yielded brittle, charred, and short filaments. Curdlan acetate propionate, another analogue with a degree of polymerization five times larger than that of paramylon mixed esters, was not extrudable due to the lack of thermoplasticity. Therefore, we herein confirmed the superiority of paramylon as a primary raw material for melt-spun filaments. Elsevier 2019-11-27 /pmc/articles/PMC6895648/ /pubmed/31844742 http://dx.doi.org/10.1016/j.heliyon.2019.e02843 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Shibakami, Motonari Sohma, Mitsugu Kijima, Norihito Nemoto, Tadashi Melt spinnabilities of thermoplastic paramylon mixed esters |
title | Melt spinnabilities of thermoplastic paramylon mixed esters |
title_full | Melt spinnabilities of thermoplastic paramylon mixed esters |
title_fullStr | Melt spinnabilities of thermoplastic paramylon mixed esters |
title_full_unstemmed | Melt spinnabilities of thermoplastic paramylon mixed esters |
title_short | Melt spinnabilities of thermoplastic paramylon mixed esters |
title_sort | melt spinnabilities of thermoplastic paramylon mixed esters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895648/ https://www.ncbi.nlm.nih.gov/pubmed/31844742 http://dx.doi.org/10.1016/j.heliyon.2019.e02843 |
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