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Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors

[Image: see text] Microspheric BN materials have high application potential because they have better fluidity and dispersion ability to endow hexagonal boron nitride (h-BN) ceramics and h-BN/polymer composites with highly desired performance. In this work, a novel synthetic route to the BN microsphe...

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Autores principales: Li, Zexia, Yang, Jingwen, Gao, Hejun, Qiao, Jiaxiao, Qiao, Wei, Wang, Peng, Zhang, Jun, Tang, Chengchun, Xue, Yanming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157864/
https://www.ncbi.nlm.nih.gov/pubmed/37151536
http://dx.doi.org/10.1021/acsomega.3c00313
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author Li, Zexia
Yang, Jingwen
Gao, Hejun
Qiao, Jiaxiao
Qiao, Wei
Wang, Peng
Zhang, Jun
Tang, Chengchun
Xue, Yanming
author_facet Li, Zexia
Yang, Jingwen
Gao, Hejun
Qiao, Jiaxiao
Qiao, Wei
Wang, Peng
Zhang, Jun
Tang, Chengchun
Xue, Yanming
author_sort Li, Zexia
collection PubMed
description [Image: see text] Microspheric BN materials have high application potential because they have better fluidity and dispersion ability to endow hexagonal boron nitride (h-BN) ceramics and h-BN/polymer composites with highly desired performance. In this work, a novel synthetic route to the BN microspheres has been developed by means of a controllable pyrolysis of polymerized spherical precursors. The precursor formation mechanism is proposed to be the F-127-induced self-assembling polymerization of a boric acid–melamine–formaldehyde (MF) colloid. It is found that ammonia-annealing of an air-pyrolysis (700 °C) intermediate causes higher BN phase transformation within final BN microspheres with more uniform diameter distribution compared to those of direct ammonia-pyrolysis of spherical precursors at the same temperatures of 1100 and 1500 °C. After ammonia-annealing and ammonia-pyrolyzed treatment at 1100 and 1500 °C, the obtained BN microspheres have a low specific surface area (SSA) property, but replacing part of melamine with dicyandiamide could increase their SSAs to more than 1000 m(2)/g. We believe that this new microspherical BN preparation with more facile and controllable operation would be well suited for industrialization.
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spelling pubmed-101578642023-05-05 Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors Li, Zexia Yang, Jingwen Gao, Hejun Qiao, Jiaxiao Qiao, Wei Wang, Peng Zhang, Jun Tang, Chengchun Xue, Yanming ACS Omega [Image: see text] Microspheric BN materials have high application potential because they have better fluidity and dispersion ability to endow hexagonal boron nitride (h-BN) ceramics and h-BN/polymer composites with highly desired performance. In this work, a novel synthetic route to the BN microspheres has been developed by means of a controllable pyrolysis of polymerized spherical precursors. The precursor formation mechanism is proposed to be the F-127-induced self-assembling polymerization of a boric acid–melamine–formaldehyde (MF) colloid. It is found that ammonia-annealing of an air-pyrolysis (700 °C) intermediate causes higher BN phase transformation within final BN microspheres with more uniform diameter distribution compared to those of direct ammonia-pyrolysis of spherical precursors at the same temperatures of 1100 and 1500 °C. After ammonia-annealing and ammonia-pyrolyzed treatment at 1100 and 1500 °C, the obtained BN microspheres have a low specific surface area (SSA) property, but replacing part of melamine with dicyandiamide could increase their SSAs to more than 1000 m(2)/g. We believe that this new microspherical BN preparation with more facile and controllable operation would be well suited for industrialization. American Chemical Society 2023-04-21 /pmc/articles/PMC10157864/ /pubmed/37151536 http://dx.doi.org/10.1021/acsomega.3c00313 Text en © 2023 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 Li, Zexia
Yang, Jingwen
Gao, Hejun
Qiao, Jiaxiao
Qiao, Wei
Wang, Peng
Zhang, Jun
Tang, Chengchun
Xue, Yanming
Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors
title Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors
title_full Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors
title_fullStr Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors
title_full_unstemmed Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors
title_short Boron Nitride Microspheres via Pyrolysis of Polymerized Precursors
title_sort boron nitride microspheres via pyrolysis of polymerized precursors
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157864/
https://www.ncbi.nlm.nih.gov/pubmed/37151536
http://dx.doi.org/10.1021/acsomega.3c00313
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