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RE含量对Mg-RE基合金组织及储氢性能的影响

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为研究RE(金属镧铈)和Ni含量对Mg-RE基合金组织和储氢性能的影响,采用感应熔炼法制备了Mg90NixRE10-x(x=4,5,6)合金,通过XRD、SEM、EDS和PCT对合金进行了表征和测试.结果表明,合金由Mg、Mg2Ni、CeMg12、Ce2Mg17、LaMg12、La2Mg17 等相组成,吸氢后形成 MgH2、Mg2NiH4、CeH2.29和LaH3.05,放氢后的相为Mg、Mg2Ni、CeH2和LaH2.活化和吸放氢动力学性能测试显示,RE和Ni元素含量比为1∶1时合金具有最佳的活化性能和吸放氢性能,最大吸氢和放氢容量分别为5.21%(质量分数)和5.19%(质量分数).合金中原位生成的REHx相以及Mg2Ni/Mg2NiH4相有利于氢原子的转移,且协同催化作用造成Mg90Ni5RE5合金具有最小的放氢反应活化能87.14 kJ/mol.根据PCT数据和Van't Hoff方程计算得到合金的吸放氢反应焓,发现合金的热力学性能与RE和Ni含量比无明显关系.
Effect of RE Content on Microstructure and Hydrogen Storage Properties of Mg-RE-based Alloys
In order to investigate the influence of RE(La and Ce)and Ni content on the microstructure and hydrogen storage performance of magnesium-based alloys,Mg90NixRE10-x(x=4,5,6)alloys are prepared using induction melting.The alloys are characterized and tested by XRD,SEM,EDS,and PCT.The results reveal that the alloy consists of phases of Mg,Mg2Ni,CeMg12,Ce2Mg17,LaMg12,and La2Mg17.After hydrogen absorption,MgH2,Mg2NiH4,CeH2.29,and LaH3.05 pha-ses are formed,while the phases after hydrogen desorption include Mg,Mg2 Ni,CeH2,and LaH2.The results of hydrogen ab-sorption and desorption kinetic test show that the optimal ratio of RE to Ni elements in the alloy is 1∶1,while the activation performance and hydrogen storage capacity are best.The maximum hydrogen absorption and desorption capacities are 5.21%and 5.19%(Mass fraction),respectively.The in situ formed REHx and Mg2Ni/Mg2NiH4 phase have synergistic catalyst effect on hydrogen transport in the alloy.The Mg90Ni5RE5 alloy exhibits the lowest activation energy during hydrogen desorp-tion reaction of 87.14 kJ/mol.Entropy change(ΔH)of the alloys,which are calculated by using the PCT data and the Van't Hoff equation,have no significant relationship with the RE content.

magnesium-based hydrogen storage alloyrare earthmicrostructurehydrogen absorption and desorption ki-neticsthermodynamics

王启昌、田红晓、刘素霞、罗龙、陈伟丽、李永治

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内蒙古科技大学理学院,内蒙古 包头 014000

镁基储氢合金 稀土 微观结构 吸放氢动力学 热力学

2024

稀土
中国稀土学会 包头稀土研究院

稀土

CSTPCD北大核心
影响因子:1.172
ISSN:1004-0277
年,卷(期):2024.45(6)