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Effect of Solvent and Functionality on the Physical Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane
[Image: see text] The present article reports the investigation on the effects of solvent and position of functionality on various physical properties of polyurethanes (PUs) based on hydroxyl-terminated polybutadiene (HTPB). The PU films (curative) were prepared by coupling HTPB (P0) with isophoron...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641248/ https://www.ncbi.nlm.nih.gov/pubmed/31458566 http://dx.doi.org/10.1021/acsomega.8b00022 |
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author | Sikder, Bikash Kumar Jana, Tushar |
author_facet | Sikder, Bikash Kumar Jana, Tushar |
author_sort | Sikder, Bikash Kumar |
collection | PubMed |
description | [Image: see text] The present article reports the investigation on the effects of solvent and position of functionality on various physical properties of polyurethanes (PUs) based on hydroxyl-terminated polybutadiene (HTPB). The PU films (curative) were prepared by coupling HTPB (P0) with isophorone diisocyanate (IPDI) in various solvent media. The PUs obtained in different solvent media displayed similar thermal profile and glass transition temperature (T(g)), but their tensile properties varied significantly. Optimized tensile properties were observed when tetrahydrofuran was used as the solvent media. In the course, the investigation of the functionality effect, tetrazole (M1, M2, and M3) were covalently attached at the terminal carbon of HTPB to obtain three modified HTPBs (P1, P2, and P3), thereby coupling with IPDI to obtain the corresponding tetrazole functional PUs films. Pristine (P0–PU) and functional PU (P1–PU, P2–PU, and P3–PU) films have similar thermal profile and T(g) (−76 °C), but they have a notable enhancement in tensile properties; for example, tensile strength and elongation at break of P0–PU were found to be 3.21 MPa and 727%, respectively, whereas these values were 4.84 MPa and 958%, respectively, in the case of P3–PU. It was observed that on increasing the number of methylene group from 1 to 3 between HTPB and tetrazole moiety, the strength of hydrogen bonding increases, which facilitates better packing of urethane network in the PU and hence improves the tensile properties. Also, modification of pristine HTPB with tetrazole derivatives enhanced the calorific values of the resulting PUs. |
format | Online Article Text |
id | pubmed-6641248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66412482019-08-27 Effect of Solvent and Functionality on the Physical Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane Sikder, Bikash Kumar Jana, Tushar ACS Omega [Image: see text] The present article reports the investigation on the effects of solvent and position of functionality on various physical properties of polyurethanes (PUs) based on hydroxyl-terminated polybutadiene (HTPB). The PU films (curative) were prepared by coupling HTPB (P0) with isophorone diisocyanate (IPDI) in various solvent media. The PUs obtained in different solvent media displayed similar thermal profile and glass transition temperature (T(g)), but their tensile properties varied significantly. Optimized tensile properties were observed when tetrahydrofuran was used as the solvent media. In the course, the investigation of the functionality effect, tetrazole (M1, M2, and M3) were covalently attached at the terminal carbon of HTPB to obtain three modified HTPBs (P1, P2, and P3), thereby coupling with IPDI to obtain the corresponding tetrazole functional PUs films. Pristine (P0–PU) and functional PU (P1–PU, P2–PU, and P3–PU) films have similar thermal profile and T(g) (−76 °C), but they have a notable enhancement in tensile properties; for example, tensile strength and elongation at break of P0–PU were found to be 3.21 MPa and 727%, respectively, whereas these values were 4.84 MPa and 958%, respectively, in the case of P3–PU. It was observed that on increasing the number of methylene group from 1 to 3 between HTPB and tetrazole moiety, the strength of hydrogen bonding increases, which facilitates better packing of urethane network in the PU and hence improves the tensile properties. Also, modification of pristine HTPB with tetrazole derivatives enhanced the calorific values of the resulting PUs. American Chemical Society 2018-03-12 /pmc/articles/PMC6641248/ /pubmed/31458566 http://dx.doi.org/10.1021/acsomega.8b00022 Text en Copyright © 2018 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 | Sikder, Bikash Kumar Jana, Tushar Effect of Solvent and Functionality on the Physical Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane |
title | Effect of Solvent and Functionality on the Physical
Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane |
title_full | Effect of Solvent and Functionality on the Physical
Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane |
title_fullStr | Effect of Solvent and Functionality on the Physical
Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane |
title_full_unstemmed | Effect of Solvent and Functionality on the Physical
Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane |
title_short | Effect of Solvent and Functionality on the Physical
Properties of Hydroxyl-Terminated Polybutadiene (HTPB)-Based Polyurethane |
title_sort | effect of solvent and functionality on the physical
properties of hydroxyl-terminated polybutadiene (htpb)-based polyurethane |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641248/ https://www.ncbi.nlm.nih.gov/pubmed/31458566 http://dx.doi.org/10.1021/acsomega.8b00022 |
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