Cyanuric Acid/Epichlorohydrin Energetic Prepolymers

Detalhes bibliográficos
Autor(a) principal: Pedroso, Luís M.
Data de Publicação: 2005
Outros Autores: Simões, Pedro, Portugal, António
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/8186
https://doi.org/10.1002/prep.200500023
Resumo: In this work new energetic prepolymers are synthesised and characterised. The structure of the prepolymers exhibits the 1,3,5-s-triazine ring with lateral chains derived from the epichlorohydrin ring opening. The chlorine atoms in these precursors are here substituted by azido groups. The presence of these groups was confirmed by FTIR and 1H NMR spectroscopy and elemental and thermal analysis. OH group content in the energetic prepolymers was found slightly lower than expected having in view the used inert precursors, while molar mass values were similar. Whereas the precursors show an endothermic thermal decomposition, the synthesised prepolymers show a clear exothermic thermal decomposition in DSC analyses. Due to the presence of the 1,3,5-s-triazine ring, the exothermic peaks were observed in a wide range of temperatures. The measured glass transition temperatures vary from -15.5 °C to -43.3 °C. High densities and a wide range of viscosities were found.
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spelling Cyanuric Acid/Epichlorohydrin Energetic PrepolymersIn this work new energetic prepolymers are synthesised and characterised. The structure of the prepolymers exhibits the 1,3,5-s-triazine ring with lateral chains derived from the epichlorohydrin ring opening. The chlorine atoms in these precursors are here substituted by azido groups. The presence of these groups was confirmed by FTIR and 1H NMR spectroscopy and elemental and thermal analysis. OH group content in the energetic prepolymers was found slightly lower than expected having in view the used inert precursors, while molar mass values were similar. Whereas the precursors show an endothermic thermal decomposition, the synthesised prepolymers show a clear exothermic thermal decomposition in DSC analyses. Due to the presence of the 1,3,5-s-triazine ring, the exothermic peaks were observed in a wide range of temperatures. The measured glass transition temperatures vary from -15.5 °C to -43.3 °C. High densities and a wide range of viscosities were found.2005info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/8186http://hdl.handle.net/10316/8186https://doi.org/10.1002/prep.200500023engPropellants, Explosives, Pyrotechnics. 30:5 (2005) 338-343Pedroso, Luís M.Simões, PedroPortugal, Antónioinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2021-11-17T14:18:53Zoai:estudogeral.uc.pt:10316/8186Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:59:17.819340Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
title Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
spellingShingle Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
Pedroso, Luís M.
title_short Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
title_full Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
title_fullStr Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
title_full_unstemmed Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
title_sort Cyanuric Acid/Epichlorohydrin Energetic Prepolymers
author Pedroso, Luís M.
author_facet Pedroso, Luís M.
Simões, Pedro
Portugal, António
author_role author
author2 Simões, Pedro
Portugal, António
author2_role author
author
dc.contributor.author.fl_str_mv Pedroso, Luís M.
Simões, Pedro
Portugal, António
description In this work new energetic prepolymers are synthesised and characterised. The structure of the prepolymers exhibits the 1,3,5-s-triazine ring with lateral chains derived from the epichlorohydrin ring opening. The chlorine atoms in these precursors are here substituted by azido groups. The presence of these groups was confirmed by FTIR and 1H NMR spectroscopy and elemental and thermal analysis. OH group content in the energetic prepolymers was found slightly lower than expected having in view the used inert precursors, while molar mass values were similar. Whereas the precursors show an endothermic thermal decomposition, the synthesised prepolymers show a clear exothermic thermal decomposition in DSC analyses. Due to the presence of the 1,3,5-s-triazine ring, the exothermic peaks were observed in a wide range of temperatures. The measured glass transition temperatures vary from -15.5 °C to -43.3 °C. High densities and a wide range of viscosities were found.
publishDate 2005
dc.date.none.fl_str_mv 2005
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/8186
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https://doi.org/10.1002/prep.200500023
url http://hdl.handle.net/10316/8186
https://doi.org/10.1002/prep.200500023
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv Propellants, Explosives, Pyrotechnics. 30:5 (2005) 338-343
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