Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide

碩士 === 中正理工學院 === 應用化學研究所 === 88 === ABSTRACT This research uses urethane (Ethyl carbamate) as starting material, to form ethyl N-nitrocarbamate through nitrated urethane. Under anhydrous conditions,the ethyl N-nitrocarbamate reacts with ammonia (NH3) to produce the ammonium...

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Main Authors: Shih-Wen Liao, 廖世文
Other Authors: Sheng-Tsair Lin
Format: Others
Language:zh-TW
Published: 2000
Online Access:http://ndltd.ncl.edu.tw/handle/29854040335009283276
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spelling ndltd-TW-088CCIT05000022015-10-13T11:50:27Z http://ndltd.ncl.edu.tw/handle/29854040335009283276 Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide 高能氧化劑ADN合成研究 Shih-Wen Liao 廖世文 碩士 中正理工學院 應用化學研究所 88 ABSTRACT This research uses urethane (Ethyl carbamate) as starting material, to form ethyl N-nitrocarbamate through nitrated urethane. Under anhydrous conditions,the ethyl N-nitrocarbamate reacts with ammonia (NH3) to produce the ammonium salt (Ammonium ethyl N-nitrocarbamate). In the final process, the ammonium salt is nitrated with nitronium tetrafluoroborate(NO2BF4). The ammonia (NH3) then reacts with the reaction mixture to produce ammonium dinitramide ( ADN ), ammonium tetrafluoroborate and regenerate the original ethyl carbamate. The physical and chemical data will be discussed in details. In the aspect of synthetic ethyl N-nitrocarbamate, this research attempts to synthesize ethyl N-nitrocarbamate via different containing acetic anhydride of the nitrating agent to associate with ethyl carbamate. It is found that using 1.0 equivalent nitric acid and 2.5 equivalent acetic anhydride as the nitrating agent to nitrate the ethyl carbamate has a better reaction condition. Finally, the reaction of synthetic ammonium dinitramide (ADN) can be prepared in the“one pot process”. The characteristic is that the intermediate does not need the process of isolation and purification, the result is the same as former experiment. Sheng-Tsair Lin 林生財 2000 學位論文 ; thesis 66 zh-TW
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description 碩士 === 中正理工學院 === 應用化學研究所 === 88 === ABSTRACT This research uses urethane (Ethyl carbamate) as starting material, to form ethyl N-nitrocarbamate through nitrated urethane. Under anhydrous conditions,the ethyl N-nitrocarbamate reacts with ammonia (NH3) to produce the ammonium salt (Ammonium ethyl N-nitrocarbamate). In the final process, the ammonium salt is nitrated with nitronium tetrafluoroborate(NO2BF4). The ammonia (NH3) then reacts with the reaction mixture to produce ammonium dinitramide ( ADN ), ammonium tetrafluoroborate and regenerate the original ethyl carbamate. The physical and chemical data will be discussed in details. In the aspect of synthetic ethyl N-nitrocarbamate, this research attempts to synthesize ethyl N-nitrocarbamate via different containing acetic anhydride of the nitrating agent to associate with ethyl carbamate. It is found that using 1.0 equivalent nitric acid and 2.5 equivalent acetic anhydride as the nitrating agent to nitrate the ethyl carbamate has a better reaction condition. Finally, the reaction of synthetic ammonium dinitramide (ADN) can be prepared in the“one pot process”. The characteristic is that the intermediate does not need the process of isolation and purification, the result is the same as former experiment.
author2 Sheng-Tsair Lin
author_facet Sheng-Tsair Lin
Shih-Wen Liao
廖世文
author Shih-Wen Liao
廖世文
spellingShingle Shih-Wen Liao
廖世文
Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide
author_sort Shih-Wen Liao
title Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide
title_short Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide
title_full Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide
title_fullStr Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide
title_full_unstemmed Studies on the Synthesis of High Energetic Oxidizer Ammonium Dinitramide
title_sort studies on the synthesis of high energetic oxidizer ammonium dinitramide
publishDate 2000
url http://ndltd.ncl.edu.tw/handle/29854040335009283276
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