Cargando…

Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin

[Image: see text] A novel addition curing ethynyl phenyl azo phenol-biphenylene resin (EPABN) was synthesized by introducing ethynylphenyl group into biphenyl novolac resin (BN) through diazo coupling reaction. Its synthesis reaction and curing mechanism were also proposed. Fourier transform infrare...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Zhihua, Li, Yujing, Li, Junjie, Gao, Yuan, Gu, Xiaohong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648784/
https://www.ncbi.nlm.nih.gov/pubmed/31459306
http://dx.doi.org/10.1021/acsomega.8b01590
_version_ 1783437942292742144
author Li, Zhihua
Li, Yujing
Li, Junjie
Gao, Yuan
Gu, Xiaohong
author_facet Li, Zhihua
Li, Yujing
Li, Junjie
Gao, Yuan
Gu, Xiaohong
author_sort Li, Zhihua
collection PubMed
description [Image: see text] A novel addition curing ethynyl phenyl azo phenol-biphenylene resin (EPABN) was synthesized by introducing ethynylphenyl group into biphenyl novolac resin (BN) through diazo coupling reaction. Its synthesis reaction and curing mechanism were also proposed. Fourier transform infrared spectroscopy and (1)H NMR spectroscopic analysis showed that the ethynylphenyl group was successfully linked to the BN molecular chain. By differential scanning calorimetry analysis, the curing process of EPABN resin was determined to be 150 °C/2 h + 172 °C/2 h + 203 °C/4 h + 255 °C/4 h + 300 °C/4 h. Gel permeation chromatography and elemental analysis showed that the introduction of ethynylphenyl group increased the number-average molecular weight and weight-average molecular weight of EPABN. Thermogravimetric analysis showed that the EPABN resin synthesized under the obtained optimum conditions has excellent heat resistance, ablation resistance, and mechanical properties. T(d)(5) and T(d)(10) of heat resistance of the cured EPABN resin are 463 and 531 °C, respectively, and its residual char yield at 700 and 1000 °C is 78.2% and 72.1%, respectively.
format Online
Article
Text
id pubmed-6648784
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-66487842019-08-27 Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin Li, Zhihua Li, Yujing Li, Junjie Gao, Yuan Gu, Xiaohong ACS Omega [Image: see text] A novel addition curing ethynyl phenyl azo phenol-biphenylene resin (EPABN) was synthesized by introducing ethynylphenyl group into biphenyl novolac resin (BN) through diazo coupling reaction. Its synthesis reaction and curing mechanism were also proposed. Fourier transform infrared spectroscopy and (1)H NMR spectroscopic analysis showed that the ethynylphenyl group was successfully linked to the BN molecular chain. By differential scanning calorimetry analysis, the curing process of EPABN resin was determined to be 150 °C/2 h + 172 °C/2 h + 203 °C/4 h + 255 °C/4 h + 300 °C/4 h. Gel permeation chromatography and elemental analysis showed that the introduction of ethynylphenyl group increased the number-average molecular weight and weight-average molecular weight of EPABN. Thermogravimetric analysis showed that the EPABN resin synthesized under the obtained optimum conditions has excellent heat resistance, ablation resistance, and mechanical properties. T(d)(5) and T(d)(10) of heat resistance of the cured EPABN resin are 463 and 531 °C, respectively, and its residual char yield at 700 and 1000 °C is 78.2% and 72.1%, respectively. American Chemical Society 2019-01-02 /pmc/articles/PMC6648784/ /pubmed/31459306 http://dx.doi.org/10.1021/acsomega.8b01590 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Li, Zhihua
Li, Yujing
Li, Junjie
Gao, Yuan
Gu, Xiaohong
Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin
title Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin
title_full Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin
title_fullStr Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin
title_full_unstemmed Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin
title_short Synthesis and Thermal Properties of Ethynyl Phenyl Azo Phenol-biphenylene Resin
title_sort synthesis and thermal properties of ethynyl phenyl azo phenol-biphenylene resin
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648784/
https://www.ncbi.nlm.nih.gov/pubmed/31459306
http://dx.doi.org/10.1021/acsomega.8b01590
work_keys_str_mv AT lizhihua synthesisandthermalpropertiesofethynylphenylazophenolbiphenyleneresin
AT liyujing synthesisandthermalpropertiesofethynylphenylazophenolbiphenyleneresin
AT lijunjie synthesisandthermalpropertiesofethynylphenylazophenolbiphenyleneresin
AT gaoyuan synthesisandthermalpropertiesofethynylphenylazophenolbiphenyleneresin
AT guxiaohong synthesisandthermalpropertiesofethynylphenylazophenolbiphenyleneresin