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《含能材料》2009年(第17卷)总目次
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《含能材料》 EI CAS CSCD 北大核心 2009年第6期I0007-I0018,共12页
关键词 能材料 《含能材料》编辑部 HTPB 推进剂 Simulation RDX 稿件处理系统 呋咱 目次
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《含能材料》2019年(第27卷)总目次
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《含能材料》 EI CAS CSCD 北大核心 2019年第12期I0010-I0030,共21页
关键词 能材料 高聚物粘结炸药 热分解动力学 《含能材料》 混合炸药 熔铸炸药 冲击点火
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缩短科技期刊论文发表周期的思考和探索——以《含能材料》为例 被引量:9
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作者 张琪 姜梅 +1 位作者 王艳秀 张桂弘 《中国科技期刊研究》 CSSCI 北大核心 2014年第12期1473-1476,共4页
在已有《含能材料》论文发表周期数据的基础上,对影响期刊论文发表周期的几个因素进行剖析,并制定缩短论文发表周期的几个措施,包括量化编辑每日最低工作量,加大初审力度,把控审稿周期,提高编辑效率,增大载文量。通过这些措施的实施,在... 在已有《含能材料》论文发表周期数据的基础上,对影响期刊论文发表周期的几个因素进行剖析,并制定缩短论文发表周期的几个措施,包括量化编辑每日最低工作量,加大初审力度,把控审稿周期,提高编辑效率,增大载文量。通过这些措施的实施,在期刊来稿数量增加的前提下,将论文发表周期由2013年(六期平均值)的340天缩短至2014年(前四期平均值)的300天。 展开更多
关键词 科技期刊 论文发表周期 来稿标准 编辑效率 审稿周期 载文量 《含能材料》
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《含能材料》编辑部信息化初探 被引量:1
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作者 姜梅 张桂弘 王艳秀 《中国科技期刊研究》 CSSCI 北大核心 2006年第4期618-620,共3页
简述了学术期刊《含能材料》在信息化建设中的相关工作,讨论了促进期刊的网络化、数字化的相关方法,以及提高科技期刊编辑信息化素养的相关实践工作。
关键词 信息化 网络化 科技期刊 网页数据库 《含能材料》 编辑部
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从《含能材料热谱集》中的DSC谱采集数据和计算动力学参数的几个问题 被引量:2
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作者 胡荣祖 董海山 +2 位作者 高胜利 赵宏安 史启祯 《含能材料》 EI CAS CSCD 2002年第4期165-167,共3页
报道了从《含能材料热谱集》中的DSC谱采集数据和计算动力学参数的几个问题。
关键词 《含能材料热谱集》 DSC谱 采集数据 计算 动力学参数 能材料
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含能快递
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作者 Aleksei B.Sheremetev 张光全 《含能材料》 EI CAS CSCD 北大核心 2012年第5期656-660,共5页
关键词 《含能材料》 英文摘要 期刊 编辑工作
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EUROPYRO 2011
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《含能材料》 EI CAS CSCD 北大核心 2011年第2期159-159,共1页
GTPS and AFP organize the 10th International Seminar EUROPYRO 2011 and the 37th International Pyrotechnics Seminar IPS,in REIMS from May 16th to May 19th 2011.EUROPYRO 2011 will focus on current status and improvement... GTPS and AFP organize the 10th International Seminar EUROPYRO 2011 and the 37th International Pyrotechnics Seminar IPS,in REIMS from May 16th to May 19th 2011.EUROPYRO 2011 will focus on current status and improvements in explosives andpyrotechnic fields for Defence,Space,industry,fireworks and safety applications. 展开更多
关键词 《含能材料》 期刊 编辑部 编辑工作 摘要
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向作者致谢
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《含能材料》 EI CAS CSCD 北大核心 2011年第6期626-626,共1页
近年,《含能材料》得到了广大作者的大力支持,为表达我们深深的谢意,特向2010~2011两年来发表两篇以上论文的作者(第一作者)赠送2012年全年《含能材料》。本刊期望在新的一年能继续得到广大作者更多的关心!欢迎赐稿!
关键词 《含能材料》 期刊 编辑部 作者
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Graphical Abstract
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《含能材料》 EI CAS CSCD 北大核心 2009年第2期I0001-I0008,共8页
关键词 《含能材料》 摘要 内容介绍 绘图
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Graphical Abstract
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《含能材料》 EI CAS CSCD 北大核心 2010年第2期I0001-I0007,共7页
关键词 《含能材料》 英文摘要 内容介绍 期刊
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Graphical Abstract
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《含能材料》 EI CAS CSCD 北大核心 2013年第6期I0002-I0009,共8页
关键词 《含能材料》 英文摘要 期刊 编辑工作
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Graphical Abstract
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《含能材料》 EI CAS CSCD 北大核心 2010年第1期I0001-I0008,共8页
关键词 《含能材料》 期刊 编辑工作 发行工作
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Graphical Abstract
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《含能材料》 EI CAS CSCD 北大核心 2010年第5期I0001-I0008,共8页
关键词 《含能材料》 英文摘要 内容介绍 期刊
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Fracture Properties of Cement Composites Reinforced with Steel Polypropylene Hybrid Fibres
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作者 郭宏定 钱春香 PietStroeven 《Journal of Southeast University(English Edition)》 EI CAS 1999年第2期55-62,共8页
Polypropylene fibres and three sizes of steel fibres reinforced concrete are discussed. The total fibres content ranges from 0 4%-0 95% by volume of concrete. A four point bending test is adopted on the notched pris... Polypropylene fibres and three sizes of steel fibres reinforced concrete are discussed. The total fibres content ranges from 0 4%-0 95% by volume of concrete. A four point bending test is adopted on the notched prisms with the size of 100?mm×100?mm×500?mm to investigate the effect of hybrid fibres on crack arresting. The research results show that there is a positive synergy effect between large steel fibres and polypropylene fibres on the load bearing capacity in the small displacement range. But this synergy effect disappears in the large displacement range. The large and strong steel fibre is better than soft polypropylene fibre and small steel fibre in the aspect of energy absorption capacity in the large displacement range. The static usage limitation for the hybrid fibres concrete with “wide peak' or “multi peaks' load CMOD pattern should be carefully selected. The ultimate load bearing capacity and the crack width or CMOD at this load level should be jointly considered. 展开更多
关键词 polypropylene fibre steel fibre fracture properties low fibre content cement based composites
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Raman Spectra of Liquid Nitromethane under Singly Shocked Conditions
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作者 王亚平 刘福生 +1 位作者 刘其军 张宁超 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2016年第2期161-166,I0001,共7页
Raman spectra of liquid nitromethane were measured in single-shock experiments using transient Raman scattering system with high sensitivity. The measurement system was combined with a two-stage light gas gun to inter... Raman spectra of liquid nitromethane were measured in single-shock experiments using transient Raman scattering system with high sensitivity. The measurement system was combined with a two-stage light gas gun to interrogate the vibrational mode-dependent behaviors of shock-compressed nitromethane molecules. Up to 12 GPa, all Raman peaks were able to be clearly detected, and showed the shock-induced shifting and broadening, but no signs of chemical changes occurred in the sample. Thus, it is concluded that chemical reactions could not be initiated in singly-shocked nitromethane below 12 GPa. 展开更多
关键词 Raman spectra Shock wave Energetic liquid explosives NITROMETHANE
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丙烯酸-2,4,6-三硝基苯乙酯的合成及热分解 被引量:2
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作者 刘强强 金波 +3 位作者 彭汝芳 舒远杰 楚士晋 董海山 《含能材料》 EI CAS CSCD 北大核心 2012年第5期579-582,共4页
以TNT、甲醛为原料,在弱碱性条件下反应合成得到2,4,6-三硝基苯乙醇(PicCH2CH2OH);PicCH2CH2OH在浓硫酸催化下和丙烯酸在甲苯中回流反应24h,合成得到丙烯酸-2,4,6-三硝基苯乙酯,产率为62%。采用紫外可见光谱(UV-Vis)、核磁共振氢谱(1HN... 以TNT、甲醛为原料,在弱碱性条件下反应合成得到2,4,6-三硝基苯乙醇(PicCH2CH2OH);PicCH2CH2OH在浓硫酸催化下和丙烯酸在甲苯中回流反应24h,合成得到丙烯酸-2,4,6-三硝基苯乙酯,产率为62%。采用紫外可见光谱(UV-Vis)、核磁共振氢谱(1HNMR)、红外光谱(FTIR)、质谱(MS)以及元素分析等对产物结构进行了表征。利用热重分析(TG)对产物热稳定性进行了研究,采用Kissinger方法和Ozawa方法计算其热分解活化能Ea分别为99.78,102.96kJ·mol-1。 展开更多
关键词 有机化学 2 4 6-三硝基苯乙醇 丙烯酸-2 4 6-三硝基苯乙酯 热稳定性 活化能
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Effect of graphite content on wear property of graphite/Al_2O_3/Mg-9Al-1Zn-0.8Ce composites 被引量:2
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作者 张美娟 杨晓红 +3 位作者 刘勇兵 曹占义 程丽任 裴亚利 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2010年第2期207-211,共5页
Using squeeze-infiltration technique, Mg-9Al-1Zn-0.8Ce composite reinforced by graphite particles and Al2O3 short fibers was fabricated. The reinforcing phases combined closely with the matrix and no agglomeration was... Using squeeze-infiltration technique, Mg-9Al-1Zn-0.8Ce composite reinforced by graphite particles and Al2O3 short fibers was fabricated. The reinforcing phases combined closely with the matrix and no agglomeration was observed. The microstructure, hardness and wear property of the composites with the graphite content of 5%, 10%, 15% and 20% were investigated, respectively. The results reveal that Ce tends to enrich around the boundaries of graphite particles and Al2O3 short fibers, and forms Al3Ce phase. When the graphite content increases to 20%, the grain size becomes small. Moreover, with increasing the graphite content, the microhardness of the composites decreases but the wear resistance increases. The graphite which works as lubricant during dry sliding process decreases the wear loss. At low load, the wear mechanism of the composite is mainly abrasive wear and oxidation wear; at high load, except that the composite with 20% graphite is still with abrasive wear and oxidation wear, the wear mechanism of other composites changes to delamination wear. 展开更多
关键词 magnesium matrix composite Ce graphite wear resistance
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Microstructure and dielectric properties of Ca-Al-B-Si-O glass/Al_2O_3 composites with various alkali oxides contents 被引量:1
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作者 刘明 周洪庆 +2 位作者 朱海奎 岳振星 赵建新 《Journal of Central South University》 SCIE EI CAS 2012年第10期2733-2739,共7页
The effects of alkali oxides (Na2O and K2O addition on both the sintering behavior and dielectric properties of Ca-AI-B-Si-O glass/Al2O3 composites were investigated by Fourier transform infrared spectroscopy (FTIR... The effects of alkali oxides (Na2O and K2O addition on both the sintering behavior and dielectric properties of Ca-AI-B-Si-O glass/Al2O3 composites were investigated by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimeter (DSC), X-ray diffractometry (XRD) and scanning electron microscopy (SEM). The results show that the increasing amount of alkali oxides in the glass causes the decrease of [SiO4], which results in the decrease of the continuity of glass network, and leads to the decrease of the softening temperature Tf of the samples and the increasing trend of crystallization. And that deduces corresponding rise of densification, dielectric constant, dielectric loss of the low temperature co-fired ceramic (LTCC) materials and the decrease of its thermal conductivity. By contrast, the borosilicate glass/A1203 composites with 1.5% (mass fraction) alkali oxides sintered at 875 ℃ for 30 rain exhibit better properties of a bulk density of 2.79 g/cm3, a porosity of 0.48%, a 2 value of 2.28 W/(m.K), a er value of 7.82 and a tand value of 9.1 × 10-4 (measured at 10 MHz). 展开更多
关键词 borosilicate glass alkali oxides Ca-AI-B-Si-O glass AL2O3 MICROSTRUCTURE thermal properties dielectric properties
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Self-assembled energetic coordination polymers based on multidentate pentazole cyclo-N_5^- 被引量:9
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作者 Peng-Cheng Wang Yuan-Gang Xu +3 位作者 Qian Wang Yan-Li Shao Qiu-Han Lin Ming Lu 《Science China Materials》 SCIE EI CSCD 2019年第1期122-129,共8页
Coordination to form polymer is emerging as a new technology for modifying or enhancing the properties of the existed energetic substances in energetic materials area. In this work, guanidine cation CN3 H6+ (Gu) and 3... Coordination to form polymer is emerging as a new technology for modifying or enhancing the properties of the existed energetic substances in energetic materials area. In this work, guanidine cation CN3 H6+ (Gu) and 3-amino-1,2,4-triazole C2H4N4(ATz) were crystallized into NaN5 and two novel energetic coordination polymers(CPs),(NaN5)5[(CH6-N3)N5](N5)3–(1) and(NaN5)2(C2H4N4)(2) were prepared respectively via a self-assembly process. The crystal structure reveals the co-existence of the chelating pentazole anion and organic component in the solid state. In polymer 1, Na+and N5– were coordinated to form a cage structure in which guanidine cation [C(NH2)3]+ was trapped;for polymer 2, a mixedligand system was observed;N5 – and ATz coordinate separately with Na+and form two independent but interweaved nets. In this way, coordination polymer has been successfully utilized to modify specific properties of energetic materials through crystallization. Benefiting from the coordination and weak interactions, the decomposition temperatures of both polymers increase from 111°C(1D structure [Na(H2 O)(N5)]?2 H2 O) to 118.4 and 126.5°C respectively. Moreover, no crystallized H2 O was generated in products to afford the anhydrous compounds of pentazole salts with high heats of formation( >800 kJ mol–1). Compared to traditional energetic materials, the advantage in heats of formation is still obvious for the cyclo-N5– based CPs, which highlights cyclo-N5– as a promising energetic precursor for high energy density materials(HEDMs). 展开更多
关键词 pentazole energetic coordination polymers SELF-ASSEMBLED STABILITY high heats of formation
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