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Synthesis and Degradation of Hexamethylene Triperoxide Diamine (HMTD)
The synthesis and decomposition of hexamethylene triperoxide diamine (HMTD) were studied. Mechanisms were proposed based on isotopic labeling and mass spectral interpretation of both condensed phase products and head‐space products. Formation of HMTD from hexamine appeared to proceed from dissociate...
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Published in: | Propellants, explosives, pyrotechnics explosives, pyrotechnics, 2016-04, Vol.41 (2), p.334-350 |
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container_end_page | 350 |
container_issue | 2 |
container_start_page | 334 |
container_title | Propellants, explosives, pyrotechnics |
container_volume | 41 |
creator | Oxley, Jimmie C. Smith, James L. Porter, Matthew McLennan, Lindsay Colizza, Kevin Zeiri, Yehuda Kosloff, Ronnie Dubnikova, Faina |
description | The synthesis and decomposition of hexamethylene triperoxide diamine (HMTD) were studied. Mechanisms were proposed based on isotopic labeling and mass spectral interpretation of both condensed phase products and head‐space products. Formation of HMTD from hexamine appeared to proceed from dissociated hexamine as evident from scrambling of the 15N label when synthesis was carried out with equal molar labeled/unlabeled hexamine. Decomposition of HMTD was considered with additives and in the presence and absence of moisture. In addition to mass spectral interpretation, density functional theory (DFT) was used to calculate energy differences of transition states and the entropies of intermediates along different possible decomposition pathways. HMTD is destabilized by water and citric acid making purification following initial synthesis essential in order to avoid unanticipated violent reaction. |
doi_str_mv | 10.1002/prep.201500151 |
format | article |
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Mechanisms were proposed based on isotopic labeling and mass spectral interpretation of both condensed phase products and head‐space products. Formation of HMTD from hexamine appeared to proceed from dissociated hexamine as evident from scrambling of the 15N label when synthesis was carried out with equal molar labeled/unlabeled hexamine. Decomposition of HMTD was considered with additives and in the presence and absence of moisture. In addition to mass spectral interpretation, density functional theory (DFT) was used to calculate energy differences of transition states and the entropies of intermediates along different possible decomposition pathways. 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HMTD is destabilized by water and citric acid making purification following initial synthesis essential in order to avoid unanticipated violent reaction.</description><subject>Decomposition</subject><subject>Decomposition mechanisms</subject><subject>Diamines</subject><subject>Entropy</subject><subject>Head-space products</subject><subject>Hexamethylene triperoxide diamine (HMTD)</subject><subject>Hexamine</subject><subject>Isotopic labels</subject><subject>Spectra</subject><subject>Synthesis</subject><subject>Synthesis (chemistry)</subject><subject>Water purification</subject><issn>0721-3115</issn><issn>1521-4087</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkN9LwzAQx4MoOKevPhd8mQ-duaZtskdxv8ROh058DGl7c5ldW5MOt__ejMkQXyQcOY7P5zi-hFwC7QKlwU1tsO4GFCLqCo5IC6IA_JAKfkxalLueAUSn5MzapUOoqxYZvGzLZoFWW0-VudfHd6Ny1eiq9Kq5N8aNWmGz2BZYojczukZTbXSOXl-rlXazzngy61-fk5O5Kixe_Pxt8joczO7GfvI0ur-7TfyMCQF-KiiHkGaMMkRAHmLO0pQLDAXLoihFYLEScZqLKATMssDdmyLN5xmCSnuUtUlnv7c21ecabSNX2mZYFKrEam0lCOpeDJQ59OoPuqzWpnTXSeACeByycLewu6cyU1lrcC5ro1fKbCVQuUtV7lKVh1Sd0NsLX7rA7T-0nD4Ppr9df-9q2-Dm4CrzIWPOeCTfHkeSJZNkGiRD-cC-AY1tiVw</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Oxley, Jimmie C.</creator><creator>Smith, James L.</creator><creator>Porter, Matthew</creator><creator>McLennan, Lindsay</creator><creator>Colizza, Kevin</creator><creator>Zeiri, Yehuda</creator><creator>Kosloff, Ronnie</creator><creator>Dubnikova, Faina</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TB</scope><scope>8FD</scope><scope>FR3</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>201604</creationdate><title>Synthesis and Degradation of Hexamethylene Triperoxide Diamine (HMTD)</title><author>Oxley, Jimmie C. ; Smith, James L. ; Porter, Matthew ; McLennan, Lindsay ; Colizza, Kevin ; Zeiri, Yehuda ; Kosloff, Ronnie ; Dubnikova, Faina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3881-b807140c303ee1e74ed3bb78e483c55be136a86bd8541ecc2115be0dfce1ab903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Decomposition</topic><topic>Decomposition mechanisms</topic><topic>Diamines</topic><topic>Entropy</topic><topic>Head-space products</topic><topic>Hexamethylene triperoxide diamine (HMTD)</topic><topic>Hexamine</topic><topic>Isotopic labels</topic><topic>Spectra</topic><topic>Synthesis</topic><topic>Synthesis (chemistry)</topic><topic>Water purification</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oxley, Jimmie C.</creatorcontrib><creatorcontrib>Smith, James L.</creatorcontrib><creatorcontrib>Porter, Matthew</creatorcontrib><creatorcontrib>McLennan, Lindsay</creatorcontrib><creatorcontrib>Colizza, Kevin</creatorcontrib><creatorcontrib>Zeiri, Yehuda</creatorcontrib><creatorcontrib>Kosloff, Ronnie</creatorcontrib><creatorcontrib>Dubnikova, Faina</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Propellants, explosives, pyrotechnics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oxley, Jimmie C.</au><au>Smith, James L.</au><au>Porter, Matthew</au><au>McLennan, Lindsay</au><au>Colizza, Kevin</au><au>Zeiri, Yehuda</au><au>Kosloff, Ronnie</au><au>Dubnikova, Faina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Degradation of Hexamethylene Triperoxide Diamine (HMTD)</atitle><jtitle>Propellants, explosives, pyrotechnics</jtitle><addtitle>Propellants, Explosives, Pyrotechnics</addtitle><date>2016-04</date><risdate>2016</risdate><volume>41</volume><issue>2</issue><spage>334</spage><epage>350</epage><pages>334-350</pages><issn>0721-3115</issn><eissn>1521-4087</eissn><abstract>The synthesis and decomposition of hexamethylene triperoxide diamine (HMTD) were studied. 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subjects | Decomposition Decomposition mechanisms Diamines Entropy Head-space products Hexamethylene triperoxide diamine (HMTD) Hexamine Isotopic labels Spectra Synthesis Synthesis (chemistry) Water purification |
title | Synthesis and Degradation of Hexamethylene Triperoxide Diamine (HMTD) |
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