首页> 外文期刊>International journal of hydrogen energy >The hydrogen storage properties and catalytic mechanism of the GuFe_2O_4-doped MgH_2 composite system
【24h】

The hydrogen storage properties and catalytic mechanism of the GuFe_2O_4-doped MgH_2 composite system

机译:掺GuFe_2O_4的MgH_2复合体系的储氢性能及催化机理

获取原文
获取原文并翻译 | 示例
       

摘要

The influence of CuFe2O4 addition on the sorption performances of MgH2 prepared by ball milling was studied for the first time. The MgH2 + 10 wt% CuFe2O4 sample exhibited an enhancement in hydrogen storage performance compared to that of as-milled MgH2, with the onset decomposition temperature decreased from 340 degrees C to 250 degrees C. Dehydrogenation kinetic result revealed that CuFe2O4-added MgH2 released around 5.3 wt% H-2 within 10 min at 320 degrees C, while the as-milled MgH2 released below 1.0 wt% H-2 under the same condition. Furthermore, about 5.0 wt% H-2 was absorbed at 250 degrees C in 30 min for the 10 wt% CuFe2O4-doped MgH2 sample. In contrast, the un-doped MgH2 only absorbed 4.0 wt% H-2 at 250 degrees C in 30 min. From the Kissinger analysis, the apparent activation energy of as-milled MgH2 was 166.0 kJ/mol and this value decreased to 113.0 kJ/mol for 10 wt% CuFe2O4-added MgH2. The enhanced sorption performance of MgH2 in the presence of CuFe2O4 is believed to be due to the role of in situ formed Fe, Mg-Cu alloy, and MgO phases as an active species to catalyse the hydrogen storage properties of MgH2. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:首次研究了CuFe2O4添加量对球磨制备的MgH2吸附性能的影响。与研磨后的MgH2相比,MgH2 + 10 wt%CuFe2O4样品的储氢性能增强,起始分解温度从340摄氏度降至250摄氏度。脱氢动力学结果表明添加CuFe2O4的MgH2释放出在320°C下10分钟内5.3%(重量)的H-2,而在相同条件下,研磨后的MgH2释放出低于1.0%(重量)的H-2。此外,对于掺杂有10wt%的CuFe 2 O 4的MgH 2样品,在250℃下在30分钟内吸收了约5.0wt%的H-2。相反,未掺杂的MgH 2在250℃下在30分钟内仅吸收4.0wt%的H-2。根据基辛格分析,研磨后的MgH2的表观活化能为166.0 kJ / mol,对于添加10 wt%CuFe2O4的MgH2,该值降至113.0 kJ / mol。据信在CuFe2O4存在下MgH2的吸附性能增强是由于原位形成的Fe,Mg-Cu合金和MgO相作为活性物质催化MgH2的储氢特性。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号