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MgH_2+20%(w)MgTiO_3复合材料的吸/放氢性能(英文)
引用本文:王家盛,韩树民,李媛,沈娜,张伟.MgH_2+20%(w)MgTiO_3复合材料的吸/放氢性能(英文)[J].物理化学学报,2014,30(12):2323-2327.
作者姓名:王家盛  韩树民  李媛  沈娜  张伟
作者单位:1. Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, Hebei Province, P. R. China; 2. State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, Hebei Province, P. R. China
基金项目:The project was supported by the National Natural Science Foundation of China(50971112,51001043);Scientific Research Projects in Colleges and Universities in Hebei Province,China(ZD2014004)~~
摘    要:为了降低MgH2的吸放氢温度,提高其吸放氢动力学性能,本文通过球磨方法制备了MgH2+20%(w)MgTiO3复合储氢材料,并研究了其储氢性能.X射线衍射(XRD)结果表明,MgTiO3在与MgH2球磨过程中生成Mg2TiO4和TiO2,并且Mg2TiO4和TiO2在体系的吸放氢过程中保持稳定,能够对MgH2的吸放氢过程产生催化作用.程序升温脱附和吸/放氢动力学测试结果表明,添加MgTiO3后MgH2的初始放氢温度从389°C降至249°C.150°C下的吸氢量从0.977%(w)提高到2.902%(w),350°C下的放氢量从2.319%(w)提高到3.653%(w).同时,MgH2放氢反应的活化能从116kJ·mol-1降至95.7kJ·mol-1.与MgH2相比,MgH2+20%(w)MgTiO3复合材料的热力学与动力学性能均有显著提高,这主要是由于球磨和放氢过程中原位生成的TiO2和Mg2TiO4具有良好的催化活性.

关 键 词:储氢性能  MgH2  MgTiO3  催化活性  活化能  
收稿时间:2014-07-14

Hydriding/Dehydriding Properties of an MgH2+20%(w) MgTiO3 Composite
WANG Jia-Sheng;HAN Shu-Min;LI Yuan;SHEN Na;ZHANG Wei.Hydriding/Dehydriding Properties of an MgH2+20%(w) MgTiO3 Composite[J].Acta Physico-Chimica Sinica,2014,30(12):2323-2327.
Authors:WANG Jia-Sheng;HAN Shu-Min;LI Yuan;SHEN Na;ZHANG Wei
Institution:1. Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, Hebei Province, P. R. China; 2. State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, Hebei Province, P. R. China
Abstract:With the aim of decreasing the dehydriding temperature and improving the hydriding/dehydriding kinetic properties of MgH2, we prepared MgH2+20%(w) MgTiO3 composite via ball-milling, and investigated the hydrogen storage properties of the composite. X- ray diffraction (XRD) results showed that the MgTiO3 decomposed into Mg2TiO4 and TiO2 during the ball-milling. These two resulting compounds remained stable during the hydriding/dehydriding processes, working as catalysts for the hydriding/dehydriding. Temperatureprogrammed- desorption (TPD) and hydriding/dehydriding kinetics tests showed that doping MgH2 with MgTiO3 lowered the onset dehydrogenation temperature of MgH2 from 389 to 249 ℃, as well as increasing the hydrogen absorption amount from 0.977%(w) to 2.902%(w) at 150 ℃, and increasing the desorption amount from 2.319% (w) to 3.653%(w) at 350 ℃. The MgTiO3 additive decreased the dehydriding activation energy of MgH2 from 116 to 95.7 kJ·mol-1. The thermodynamic and kinetic performance of the MgH2+20%(w) MgTiO3 composite was significantly improved compared with pristine MgH2, which was attributed to the high catalytic activity of the (insitu formed) TiO2 and Mg2TiO4 during the ball-milling and dehydriding processes.
Keywords:Hydrogen storage property  MgH2  MgTiO3  Catalytic activity  Activation energy  
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