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高浓度过氧化氢分解用MnO x /CeO 2 -Al 2 O 3 整体催化剂 高浓度过氧化氢分解用MnO x /CeO 2 -Al 2 O 3 整体催化剂
Q3 Engineering Pub Date : 2014-01-01 DOI: 10.3969/J.ISSN.1006-9941.2014.02.005
吴春田, 王晓东, 周秀楠, 杨天卓, 张尚进, 张涛
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引用次数: 0
高能氧化剂N-氧化-3′3-偶氮-双(6-氨基-1,2,4,5-四嗪)合成与性能 高能氧化剂N-氧化-3′3-偶氮-双(6-氨基-1,2,4,5-四嗪)合成与性能
Q3 Engineering Pub Date : 2014-01-01 DOI: 10.3969/J.ISSN.1006-9941.2014.01.002
罗义芬, 周群, 王伯周, 李辉, 周诚, 李吉祯, 樊学忠
以3,6-二氨基-1,2,4,5-四嗪为原料,经高锰酸钾、双氧水/三氟乙酸酐两步氧化反应得到高能氧化剂 N-氧化-3′3-偶氮-双(6-氨基-1,2,4,5-四嗪)(DAATO3.5),总收率为53.1%。用红外光谱、核磁共振以及元素分析表征了其结构。探讨了双氧水/三氟乙酸酐氧化的反应机理。确定其适宜反应条件为:3,3′-偶氮-(6-氨基-1,2,4,5-四嗪)( DAAT)/( CF3CO)2O/H2O2料比1∶12.5∶11,反应时间20 h,反应温度20~25℃。用DSC和TG-DTG 研究了DAATO3.5的热行为,其热分解峰温为254.6℃,表明 DAATO3.5有良好的热稳定性。DAATO3.5密度为1.840 g·cm-3,摩擦感度100%(90°摆角),撞击感度100%(10 kg,25 cm)。
以3,6-二氨基-1,2,4,5-四嗪为原料,经高锰酸钾、双氧水/三氟乙酸酐两步氧化反应得到高能氧化剂 N-氧化-3′3-偶氮-双(6-氨基-1,2,4,5-四嗪)(DAATO3.5),总收率为53.1%。用红外光谱、核磁共振以及元素分析表征了其结构。探讨了双氧水/三氟乙酸酐氧化的反应机理。确定其适宜反应条件为:3,3′-偶氮-(6-氨基-1,2,4,5-四嗪)( DAAT)/( CF3CO)2O/H2O2料比1∶12.5∶11,反应时间20 h,反应温度20~25℃。用DSC和TG-DTG 研究了DAATO3.5的热行为,其热分解峰温为254.6℃,表明 DAATO3.5有良好的热稳定性。DAATO3.5密度为1.840 g·cm-3,摩擦感度100%(90°摆角),撞击感度100%(10 kg,25 cm)。
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引用次数: 0
碳纳米管对Zr/KClO 4 烟火剂的热行为和光辐射性能的影响 碳纳米管对Zr/KClO 4 烟火剂的热行为和光辐射性能的影响
Q3 Engineering Pub Date : 2014-01-01 DOI: 10.3969/J.ISSN.1006-9941.2014.01.016
刘黎明, 康晓丽, 易勇, 张红芳, 罗江山, 唐永建
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引用次数: 0
6-偕二硝基乙烯基-4,5,8-三硝基-5,6,7,8-四氢化-4H-咪唑烷并[4,5-e]呋咱并[3,4-b]哌嗪的合成 6-偕二硝基乙烯基-4,5,8-三硝基-5,6,7,8-四氢化-4H-咪唑烷并[4,5-e]呋咱并[3,4-b]哌嗪的合成
Q3 Engineering Pub Date : 2014-01-01 DOI: 10.3969/j.issn.1006-9941.2014.02.031
霍欢, 王伯周, 廉鹏, 来蔚鹏, 李辉, 葛忠学
以FOX-7和乙二醛为原料,经过两步缩合环化反应和硝化反应,首次设计并合成出了一种新型的呋咱稠环硝胺化合物6-偕二硝基乙烯基-4,5,8-三硝基-5,6,7,8-四氢化-4H-咪唑烷并[4,5-e]呋咱并[3,4-b]哌嗪(PNEIFP)。采用Gaussian 09程序和VLW方程计算PNEIFP的密度、生成焓和爆速分别为2.02 g·cm^-3、724.1 kJ·mol^-1和9681.0 m·s^-1。利用TLC跟踪实验的方法,确定PNEIFP室温下易分解。
以FOX-7和乙二醛为原料,经过两步缩合环化反应和硝化反应,首次设计并合成出了一种新型的呋咱稠环硝胺化合物6-偕二硝基乙烯基-4,5,8-三硝基-5,6,7,8-四氢化-4H-咪唑烷并[4,5-e]呋咱并[3,4-b]哌嗪(PNEIFP)。采用Gaussian 09程序和VLW方程计算PNEIFP的密度、生成焓和爆速分别为2.02 g·cm^-3、724.1 kJ·mol^-1和9681.0 m·s^-1。利用TLC跟踪实验的方法,确定PNEIFP室温下易分解。
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引用次数: 0
DNTF/RDX-CMDB推进剂低温力学性能 DNTF/RDX-CMDB推进剂低温力学性能
Q3 Engineering Pub Date : 2013-08-25 DOI: 10.3969/J.ISSN.1006-9941.2011.03.009
肖玮, 李亮亮, 王江宁, 苏健军, 王世英, 董树南, 屈可朋
用单轴抗拉实验、动态力学分析仪和简支梁抗冲实验研究了不同3,4-二硝基呋咱基氧化呋咱(DNTF)/ RDX配比对DNTF/RDX改性双基(CMDB)推进剂(DNTF/RDX-CMDB,DFR推进剂)力学性能的影响。获得了-40 ℃下DFR推进剂的抗拉强度( σ m )、断裂延伸率( e m )及抗冲强度( a K )。根据“时间-温度”等效原理的WLF方程获得了DFR推进剂 β 松弛阶段的动态特征量黏弹系数( C 1 g )。分析了组分含量对各力学性能的影响和 σ m 、 e m 的变化规律。结果表明:低温下的 σ m 、 e m 和 a K 均与增塑剂含量间存在相关性。增塑剂含量减小,粘弹系数增加,NC分子侧基的“自由体积”下降,导致抗拉强度、断裂延伸率等力学性能降低。
用单轴抗拉实验、动态力学分析仪和简支梁抗冲实验研究了不同3,4-二硝基呋咱基氧化呋咱(DNTF)/ RDX配比对DNTF/RDX改性双基(CMDB)推进剂(DNTF/RDX-CMDB,DFR推进剂)力学性能的影响。获得了-40 ℃下DFR推进剂的抗拉强度( σ m )、断裂延伸率( e m )及抗冲强度( a K )。根据“时间-温度”等效原理的WLF方程获得了DFR推进剂 β 松弛阶段的动态特征量黏弹系数( C 1 g )。分析了组分含量对各力学性能的影响和 σ m 、 e m 的变化规律。结果表明:低温下的 σ m 、 e m 和 a K 均与增塑剂含量间存在相关性。增塑剂含量减小,粘弹系数增加,NC分子侧基的“自由体积”下降,导致抗拉强度、断裂延伸率等力学性能降低。
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引用次数: 0
Performances of the binder film of BAMO-r-GAP copolymer/N100/IPDI curing system BAMO-r-GAP共聚物/N100/IPDI固化体系粘结膜性能研究
Q3 Engineering Pub Date : 2013-01-01 DOI: 10.3969/J.ISSN.1006-9941.2013.01.015
Yibo Zhao, Yun-jun Luo, Chi Zhang
The binder film of 3, 3-bis(azidomethy) oxetane-r-(glycidyl azide)(BAMO-r-GAP) copolymer/N100/IPDI system was synthesized using BAMO-r-GAP copolymer as pre-polymer, N100 and IPDI as curing agent and BDO as chain extended agent. The Fourier transform infrared(FT-IR) spectrometer, differential scanning calorimetry(DSC) and thermogravimetry-derivative thermogravimetry(TG-DTG) were used to characterize the binder film, and the mechanical properties was also measured. Results show that the tensile strength of the binder film is raised to 0.87 MPa, and the breaking elongation is above 106%. The glass transition temperature (Tg) of the binder film is about -50°C and the thermal decomposition starts at 217.0°C, which means the binder film has good thermal stability.
以BAMO-r-GAP共聚物为预聚体,N100和IPDI为固化剂,BDO为扩链剂,合成了3,3 -双(叠氮氧基)氧烷-r-(叠氮甘油酯)(BAMO-r-GAP)共聚物/N100/IPDI体系的粘结膜。采用傅里叶变换红外光谱仪(FT-IR)、差示扫描量热仪(DSC)和热重-导数热重仪(TG-DTG)对粘结膜进行表征,并对其力学性能进行了测试。结果表明:粘结膜的抗拉强度提高到0.87 MPa,断裂伸长率达到106%以上。粘结膜的玻璃化转变温度(Tg)约为-50℃,热分解开始于217.0℃,说明粘结膜具有良好的热稳定性。
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引用次数: 0
Solubility of RDX in melting DNAN/MNA RDX在熔融DNAN/MNA中的溶解度
Q3 Engineering Pub Date : 2012-01-01 DOI: 10.3969/J.ISSN.1006-9941.2012.04.012
G. Luo, Hui Huang, Shuai Zhang, Pingsheng Wang, Zhongzhan Cai, Yong Zhang
High performance liquid chromatography (HPLC) was employed to analysis the solubility of RDX in melting DNAN/MNA at the range of 87°C to 95.3°C. The optimal chromatography conditions were as following: mobile phase is methanol/water=6/4 (V/V), and flow rate 1.0 mL·min -1, and wavelength of detector 254 nm, and injection volume 5.0 μL. The influence of particle size, equilibration time and temperature programming on solubility was studied. Under the optimum condition, the curve of the solubility of RDX in DNAN/MNA as a function of temperature was built. Results show that the solubility of RDX increases with increasing of the temperature.
采用高效液相色谱法(HPLC)分析了RDX在87℃~ 95.3℃熔融DNAN/MNA中的溶解度。最佳色谱条件为:流动相为甲醇/水=6/4 (V/V),流速1.0 mL·min -1,检测器波长254 nm,进样量5.0 μL。研究了粒径、平衡时间和温度规划对溶解度的影响。在最佳条件下,建立了RDX在DNAN/MNA中的溶解度随温度的变化曲线。结果表明,RDX的溶解度随温度的升高而增大。
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引用次数: 1
3-硝基-1,2,4-三唑-5-酮脒基脲盐的合成与表征 3-硝基-1,2,4-三唑-5-酮脒基脲盐的合成与表征
Q3 Engineering Pub Date : 2011-01-01 DOI: 10.3969/j.issn.1006-9941.2014.02.013
黄新萍, 常佩, 王伯周, 陈智群, 来蔚鹏, 毕福强
为了克服3-硝基-1,2,4-三唑-5-酮(NTO)的酸性,设计了新的含能离子化合物3-硝基-1,2,4-三唑-5-酮脒基脲盐(GUNTO),以NTO和脒基脲盐酸盐为原料,采用一锅法和分步法两种方法合成了GUNTO,收率均高于85%。用红外光谱、核磁共振、质谱、元素分析和X-射线单晶衍射表征了它的结构。研究了GUNTO的物化性质与爆轰性能。借助晶体密度1.72 g·cm^-3和理论计算的生成焓-347.35 kJ·mol^-1,运用Kamlet公式预估爆速为6683.49 m·s^-1、爆压为19.27 GPa。实测撞击感度、摩擦感度均为0%,特性落高H50大于125.8 cm,10℃·min^-1时DSC曲线的峰温为236.8℃。与其他NTO胺盐相比,GUNTO氮含量较高、热稳定性好、感度低。
为了克服3-硝基-1,2,4-三唑-5-酮(NTO)的酸性,设计了新的含能离子化合物3-硝基-1,2,4-三唑-5-酮脒基脲盐(GUNTO),以NTO和脒基脲盐酸盐为原料,采用一锅法和分步法两种方法合成了GUNTO,收率均高于85%。用红外光谱、核磁共振、质谱、元素分析和X-射线单晶衍射表征了它的结构。研究了GUNTO的物化性质与爆轰性能。借助晶体密度1.72 g·cm^-3和理论计算的生成焓-347.35 kJ·mol^-1,运用Kamlet公式预估爆速为6683.49 m·s^-1、爆压为19.27 GPa。实测撞击感度、摩擦感度均为0%,特性落高H50大于125.8 cm,10℃·min^-1时DSC曲线的峰温为236.8℃。与其他NTO胺盐相比,GUNTO氮含量较高、热稳定性好、感度低。
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引用次数: 0
3-氨基-2,4,6-三硝基苯甲醚的合成及性能 3-氨基-2,4,6-三硝基苯甲醚的合成及性能
Q3 Engineering Pub Date : 2010-01-01 DOI: 10.3969/J.ISSN.1006-9941.2010.02.003
张学梅, 董海山, 夏云霞, 刘晓峰
为了寻找含能共熔物中的辅助组分,合成了3-氨基-2,4,6-三硝基苯甲醚,并对其性能进行了初步研究。以市售苦味酸为原料,经过甲基化、替代氢的亲核取代反应,得到目标产物,产率达76%以上。产物和中间体的结构通过傅立叶红外光谱、核磁共振氢谱、元素分析进行了表征。对甲基化反应和替代氢的亲核取代反应机理进行了探讨。通过DSC和TG研究了3-氨基-2,4,6-三硝基苯甲醚的热分解性能,其吸热峰温为133.77℃,放热峰温254.10℃,在199.6℃,质量损失1.71%左右。采用特性落高法测得其撞击感度H50为82.5cm,爆炸概率法测得其摩擦感度为0%、其静电火花感度为V50=11.42kV,E50=1.99J。采用VLW软件计算理论爆速为7.459km.s-1(ρ=1.709g.cm-3),理论爆压为22.9GPa(ρ=1.709g.cm-3)。研究结果表明,3-氨基-2,4,6-三硝基苯甲醚具有较好的热稳定性,其感度低于TNT,理论爆速和爆压高于TNT,是一种性能良好的高能低感炸药,可作为辅助组分用于含能共熔物中。
为了寻找含能共熔物中的辅助组分,合成了3-氨基-2,4,6-三硝基苯甲醚,并对其性能进行了初步研究。以市售苦味酸为原料,经过甲基化、替代氢的亲核取代反应,得到目标产物,产率达76%以上。产物和中间体的结构通过傅立叶红外光谱、核磁共振氢谱、元素分析进行了表征。对甲基化反应和替代氢的亲核取代反应机理进行了探讨。通过DSC和TG研究了3-氨基-2,4,6-三硝基苯甲醚的热分解性能,其吸热峰温为133.77℃,放热峰温254.10℃,在199.6℃,质量损失1.71%左右。采用特性落高法测得其撞击感度H50为82.5cm,爆炸概率法测得其摩擦感度为0%、其静电火花感度为V50=11.42kV,E50=1.99J。采用VLW软件计算理论爆速为7.459km.s-1(ρ=1.709g.cm-3),理论爆压为22.9GPa(ρ=1.709g.cm-3)。研究结果表明,3-氨基-2,4,6-三硝基苯甲醚具有较好的热稳定性,其感度低于TNT,理论爆速和爆压高于TNT,是一种性能良好的高能低感炸药,可作为辅助组分用于含能共熔物中。
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引用次数: 0
期刊
Hanneng Cailiao/Chinese Journal of Energetic Materials
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