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LaNi5合金的吸氢动力学

HYDROGEN ABSORPTION KINETICS OF LaNi5 ALLOY

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【作者】 宏存茂林秋竹韩德刚

【Author】 Hong Cunmao;Lin Qiuzhu;Han Degang Department of Chemistry, Peking University, Beijing 100871

【机构】 北京大学化学系北京大学化学系 北京 100871北京 100871北京 100871

【摘要】 研究了LaNi5-H体系的吸氢反应动力学。在吸放氢可逆反应同时考虑的情况下,求得了速度方程的解析解。在α相区20—50℃的温度范围内,吸氢速度常数kα为0.08—0.41s-1;脱氢速度常数kd为4.8—25MPa·s-1。吸氢反应的表观活化能Eα为35kJ(molH2-1。在α+β相区的吸氢较α相区慢得多。起始阶段吸氢速度对氢压为一级,反应受氢化物表面上氢分子解离控制。随着吸氢反应深度的增大,吸氢速度变为固相中的界面反应控制。速度常数受温度的影响很小。α+β相区的压力平台前半段和后半段有着不同的吸氢速度。

【Abstract】 Hydrogen absorption kinetics of LaNi5-H system in α and α+β phases has beeninvestigated. Taking the reversibility of hydrogen absorption and desorption into ac-count,an analytical solution has been obtained for the α phase.In a temperature rangeof 20--50℃, the rate constant of hydrogen absorption, ka, was found to be 0.08-0.41s-1 and that of hydrogen desorption, ka, 4.8--25 MPa·s-1 respectively.The ap-parent activation energy of hydrogen absorption was 35kJ(mol H2-1. Hydrogen ab-sorption in α+β phase was slower than that of the α-phase.The initial rate of hydrogenabsorption is in first order with the hydrogen pressure used.The reaction is controlledby the dissociation of hydrogen on the alloy surface. With increasing of the reactiondepth, the controlling step will shift to the reaction occuring on the α-β interface.The rate constants are weakly dependent on the temperature.The hydrogen absorptionrates on the initial and final stage of the pressure plateau in α+β phase are obviou-sly different.

【关键词】 合金动力学
【Key words】 HydrogenAlloyKinetics
【基金】 国家科委资助863项目
  • 【文献出处】 物理化学学报 ,Acta Physico-chimica Sinica , 编辑部邮箱 ,1992年05期
  • 【被引频次】8
  • 【下载频次】159
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