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Synthesis, Structures, and Properties of a New Pentaerythritol-Derived Flame Retardant Used in Polyamide 66
[Image: see text] A melting phosphorous-based flame retardant (FR) named as diphenyl phosphoryl (DPP)–PEPA is synthesized from 2,6,7-trioxa-1-phosphabicyclo-(2.2.2)-octane-4-methanol (PEPA) and diphenyl phosphoryl chloride. The melting DPP–PEPA FR possesses high thermostability with T(5wt%) at 344 °...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154225/ https://www.ncbi.nlm.nih.gov/pubmed/34056440 http://dx.doi.org/10.1021/acsomega.1c01385 |
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author | Guo, Shangzhen Xu, Jiaqi Ni, Xiuyuan |
author_facet | Guo, Shangzhen Xu, Jiaqi Ni, Xiuyuan |
author_sort | Guo, Shangzhen |
collection | PubMed |
description | [Image: see text] A melting phosphorous-based flame retardant (FR) named as diphenyl phosphoryl (DPP)–PEPA is synthesized from 2,6,7-trioxa-1-phosphabicyclo-(2.2.2)-octane-4-methanol (PEPA) and diphenyl phosphoryl chloride. The melting DPP–PEPA FR possesses high thermostability with T(5wt%) at 344 °C, which can match the melt-spinning of engineering plastics at high temperatures. The structure of DPP–PEPA is defined by nuclear magnetic resonance and infrared spectrometry. The influences of DPP–PEPA on polyamide 6,6 (PA66) are assessed in terms of rheology parameters and crystallinity. It is observed that the flame retardancy of PA66 is greatly improved when DPP–PEPA is added to the PA66 resin. The results show that the modified PA66 has limited oxygen index as high as 29.4%, and the compact char layers are obviously formed on top of the burned samples. As compared to the pure PA66, the peak heat release rate and the average effective heat of combustion are decreased by 26.5 and 19.3%, respectively. It is obtained that the value of flame retardancy index is 1.4, indicating high efficiency of the entire flame retardancy. Moreover, pyrolysis of DPP–PEPA is carried out at different temperatures for identifying gaseous products and types of flame retardancy. |
format | Online Article Text |
id | pubmed-8154225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-81542252021-05-27 Synthesis, Structures, and Properties of a New Pentaerythritol-Derived Flame Retardant Used in Polyamide 66 Guo, Shangzhen Xu, Jiaqi Ni, Xiuyuan ACS Omega [Image: see text] A melting phosphorous-based flame retardant (FR) named as diphenyl phosphoryl (DPP)–PEPA is synthesized from 2,6,7-trioxa-1-phosphabicyclo-(2.2.2)-octane-4-methanol (PEPA) and diphenyl phosphoryl chloride. The melting DPP–PEPA FR possesses high thermostability with T(5wt%) at 344 °C, which can match the melt-spinning of engineering plastics at high temperatures. The structure of DPP–PEPA is defined by nuclear magnetic resonance and infrared spectrometry. The influences of DPP–PEPA on polyamide 6,6 (PA66) are assessed in terms of rheology parameters and crystallinity. It is observed that the flame retardancy of PA66 is greatly improved when DPP–PEPA is added to the PA66 resin. The results show that the modified PA66 has limited oxygen index as high as 29.4%, and the compact char layers are obviously formed on top of the burned samples. As compared to the pure PA66, the peak heat release rate and the average effective heat of combustion are decreased by 26.5 and 19.3%, respectively. It is obtained that the value of flame retardancy index is 1.4, indicating high efficiency of the entire flame retardancy. Moreover, pyrolysis of DPP–PEPA is carried out at different temperatures for identifying gaseous products and types of flame retardancy. American Chemical Society 2021-05-10 /pmc/articles/PMC8154225/ /pubmed/34056440 http://dx.doi.org/10.1021/acsomega.1c01385 Text en © 2021 The Authors. Published by American Chemical Society 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 | Guo, Shangzhen Xu, Jiaqi Ni, Xiuyuan Synthesis, Structures, and Properties of a New Pentaerythritol-Derived Flame Retardant Used in Polyamide 66 |
title | Synthesis, Structures, and Properties of a New Pentaerythritol-Derived
Flame Retardant Used in Polyamide 66 |
title_full | Synthesis, Structures, and Properties of a New Pentaerythritol-Derived
Flame Retardant Used in Polyamide 66 |
title_fullStr | Synthesis, Structures, and Properties of a New Pentaerythritol-Derived
Flame Retardant Used in Polyamide 66 |
title_full_unstemmed | Synthesis, Structures, and Properties of a New Pentaerythritol-Derived
Flame Retardant Used in Polyamide 66 |
title_short | Synthesis, Structures, and Properties of a New Pentaerythritol-Derived
Flame Retardant Used in Polyamide 66 |
title_sort | synthesis, structures, and properties of a new pentaerythritol-derived
flame retardant used in polyamide 66 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8154225/ https://www.ncbi.nlm.nih.gov/pubmed/34056440 http://dx.doi.org/10.1021/acsomega.1c01385 |
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