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Thermal Decomposition of Energetic Materials 72: Unusual Behavior of Substituted Furazan Compounds upon Flash Pyrolysis
The behavior upon flash pyrolysis is described for two neutral furazan compounds of stoichiometry R 1R 2C 2N 2O (R 1 = −NO 2 or −NH 2 and R 2 = −NHNO 2) and four salts (Na +, NH 4 +, NH 2NH 3 +, and NH 3OH +) in which R 1 = −NO 2 and R 2 = −NNO 2 −. Highly exothermic decomposition occurred in all ca...
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Published in: | Combustion and flame 1998-08, Vol.114 (3), p.569-576 |
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container_title | Combustion and flame |
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creator | Williams, G.K. Brill, T.B. |
description | The behavior upon flash pyrolysis is described for two neutral furazan compounds of stoichiometry R
1R
2C
2N
2O (R
1 = −NO
2 or −NH
2 and R
2 = −NHNO
2) and four salts (Na
+, NH
4
+, NH
2NH
3
+, and NH
3OH
+) in which R
1 = −NO
2 and R
2 = −NNO
2
−. Highly exothermic decomposition occurred in all cases. Rapid-scan IR spectroscopy was used to quantify the IR-active gaseous products in real time, while mass spectrometry was used to identify N
2 and, in two cases, O
2. Good to excellent mass balance was obtained for each compound. Although only a few relationships exist between the stoichiometry and the decomposition characteristics, several compounds exhibit surprising and novel behavior. The most unusual behavior occurs when R
1 = −NO
2 and R
2 = −N(H)NO
2. Linear cyanogen-N-oxide NCCNO is formed by opening of the furazan ring and stripping of the substituents. A complex reaction between the substituents produces HNO
3 and N
2 while leaving residual NO
2, rather than producing N
2O and HNO
3 by a simple reaction. |
doi_str_mv | 10.1016/S0010-2180(97)00330-1 |
format | article |
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1R
2C
2N
2O (R
1 = −NO
2 or −NH
2 and R
2 = −NHNO
2) and four salts (Na
+, NH
4
+, NH
2NH
3
+, and NH
3OH
+) in which R
1 = −NO
2 and R
2 = −NNO
2
−. Highly exothermic decomposition occurred in all cases. Rapid-scan IR spectroscopy was used to quantify the IR-active gaseous products in real time, while mass spectrometry was used to identify N
2 and, in two cases, O
2. Good to excellent mass balance was obtained for each compound. Although only a few relationships exist between the stoichiometry and the decomposition characteristics, several compounds exhibit surprising and novel behavior. The most unusual behavior occurs when R
1 = −NO
2 and R
2 = −N(H)NO
2. Linear cyanogen-N-oxide NCCNO is formed by opening of the furazan ring and stripping of the substituents. A complex reaction between the substituents produces HNO
3 and N
2 while leaving residual NO
2, rather than producing N
2O and HNO
3 by a simple reaction.</description><identifier>ISSN: 0010-2180</identifier><identifier>EISSN: 1556-2921</identifier><identifier>DOI: 10.1016/S0010-2180(97)00330-1</identifier><identifier>CODEN: CBFMAO</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Applied sciences ; Combustion. Flame ; Energy ; Energy. Thermal use of fuels ; Exact sciences and technology ; Miscellaneous ; Theoretical studies. Data and constants. Metering</subject><ispartof>Combustion and flame, 1998-08, Vol.114 (3), p.569-576</ispartof><rights>1998 Elsevier Science Inc.</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-8ee52dc88545ecd46df1b684d534ce7c93e05158f76f96c4c340ad77509be38b3</citedby><cites>FETCH-LOGICAL-c367t-8ee52dc88545ecd46df1b684d534ce7c93e05158f76f96c4c340ad77509be38b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2295077$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Williams, G.K.</creatorcontrib><creatorcontrib>Brill, T.B.</creatorcontrib><title>Thermal Decomposition of Energetic Materials 72: Unusual Behavior of Substituted Furazan Compounds upon Flash Pyrolysis</title><title>Combustion and flame</title><description>The behavior upon flash pyrolysis is described for two neutral furazan compounds of stoichiometry R
1R
2C
2N
2O (R
1 = −NO
2 or −NH
2 and R
2 = −NHNO
2) and four salts (Na
+, NH
4
+, NH
2NH
3
+, and NH
3OH
+) in which R
1 = −NO
2 and R
2 = −NNO
2
−. Highly exothermic decomposition occurred in all cases. Rapid-scan IR spectroscopy was used to quantify the IR-active gaseous products in real time, while mass spectrometry was used to identify N
2 and, in two cases, O
2. Good to excellent mass balance was obtained for each compound. Although only a few relationships exist between the stoichiometry and the decomposition characteristics, several compounds exhibit surprising and novel behavior. The most unusual behavior occurs when R
1 = −NO
2 and R
2 = −N(H)NO
2. Linear cyanogen-N-oxide NCCNO is formed by opening of the furazan ring and stripping of the substituents. A complex reaction between the substituents produces HNO
3 and N
2 while leaving residual NO
2, rather than producing N
2O and HNO
3 by a simple reaction.</description><subject>Applied sciences</subject><subject>Combustion. Flame</subject><subject>Energy</subject><subject>Energy. Thermal use of fuels</subject><subject>Exact sciences and technology</subject><subject>Miscellaneous</subject><subject>Theoretical studies. Data and constants. Metering</subject><issn>0010-2180</issn><issn>1556-2921</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkEtvEzEUhS0EEqHlJyB5gRAshvoxfgwbBKGBSkUgtV1bjn2HGE3GwXdclP56Jk3VLau7-c53dA8hrzh7zxnXZ1eMcdYIbtnbzrxjTErW8CdkwZXSjegEf0oWj8hz8gLxN2PMtFIuyN_rDZStH-gXCHm7y5imlEeae3o-QvkFUwr0u5-gJD8gNeIDvRkr1jnwGTb-NuVyYK_qGqc01QkiXdXi7_xIlwddHSPSupuNq8Hjhv7clzzsMeEpedbPRnj5cE_Izer8evmtufzx9WL56bIJUpupsQBKxGCtahWE2OrY87W2bVSyDWBCJ4EprmxvdN_p0AbZMh-NUaxbg7RreULeHL27kv9UwMltEwYYBj9CruiEtkJwbWdQHcFQMmKB3u1K2vqyd5y5w8zufmZ32NB1xt3P7Pice_1Q4DH4oS9-DAkfw0J0ihkzYx-PGMzP3iYoDkOCMUBMBcLkYk7_KfoHeYmSog</recordid><startdate>19980801</startdate><enddate>19980801</enddate><creator>Williams, G.K.</creator><creator>Brill, T.B.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope></search><sort><creationdate>19980801</creationdate><title>Thermal Decomposition of Energetic Materials 72: Unusual Behavior of Substituted Furazan Compounds upon Flash Pyrolysis</title><author>Williams, G.K. ; Brill, T.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-8ee52dc88545ecd46df1b684d534ce7c93e05158f76f96c4c340ad77509be38b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Applied sciences</topic><topic>Combustion. Flame</topic><topic>Energy</topic><topic>Energy. Thermal use of fuels</topic><topic>Exact sciences and technology</topic><topic>Miscellaneous</topic><topic>Theoretical studies. Data and constants. Metering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Williams, G.K.</creatorcontrib><creatorcontrib>Brill, T.B.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Combustion and flame</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Williams, G.K.</au><au>Brill, T.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermal Decomposition of Energetic Materials 72: Unusual Behavior of Substituted Furazan Compounds upon Flash Pyrolysis</atitle><jtitle>Combustion and flame</jtitle><date>1998-08-01</date><risdate>1998</risdate><volume>114</volume><issue>3</issue><spage>569</spage><epage>576</epage><pages>569-576</pages><issn>0010-2180</issn><eissn>1556-2921</eissn><coden>CBFMAO</coden><abstract>The behavior upon flash pyrolysis is described for two neutral furazan compounds of stoichiometry R
1R
2C
2N
2O (R
1 = −NO
2 or −NH
2 and R
2 = −NHNO
2) and four salts (Na
+, NH
4
+, NH
2NH
3
+, and NH
3OH
+) in which R
1 = −NO
2 and R
2 = −NNO
2
−. Highly exothermic decomposition occurred in all cases. Rapid-scan IR spectroscopy was used to quantify the IR-active gaseous products in real time, while mass spectrometry was used to identify N
2 and, in two cases, O
2. Good to excellent mass balance was obtained for each compound. Although only a few relationships exist between the stoichiometry and the decomposition characteristics, several compounds exhibit surprising and novel behavior. The most unusual behavior occurs when R
1 = −NO
2 and R
2 = −N(H)NO
2. Linear cyanogen-N-oxide NCCNO is formed by opening of the furazan ring and stripping of the substituents. A complex reaction between the substituents produces HNO
3 and N
2 while leaving residual NO
2, rather than producing N
2O and HNO
3 by a simple reaction.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><doi>10.1016/S0010-2180(97)00330-1</doi><tpages>8</tpages></addata></record> |
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language | eng |
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source | ScienceDirect Freedom Collection |
subjects | Applied sciences Combustion. Flame Energy Energy. Thermal use of fuels Exact sciences and technology Miscellaneous Theoretical studies. Data and constants. Metering |
title | Thermal Decomposition of Energetic Materials 72: Unusual Behavior of Substituted Furazan Compounds upon Flash Pyrolysis |
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