摘要
采用机械合金化法制备了Mg2Ni-1.00%Pd(质量分数)合金粉末,用XRD及AFM等分析表征了材料吸放氢前后相和微观结构的变化,测定了Mg2Ni-1.00%Pd合金的吸放氢动力学曲线和PCT曲线。结果表明,机械合金化制备的Mg2Ni-1.00%Pd合金粉末颗粒尺寸在10-50 nm之间;添加1.00%Pd机械球磨,可显著地改善纳米Mg2Ni合金的吸/放氢动力学性能,在初始氢压为1.17 MPa、温度为423和473 K时,同熔炼法制备的合金相比,材料无需活化即可快速吸氢;PCT曲线上有明显的坪台区,而且坪宽较长,有一定的滞后效应且滞后系数随温度的升高而降低;同熔炼法制备的Mg2Ni合金相比,纳米Mg2Ni-1.00%Pd合金吸氢时的焓变值减小,放氢时焓变值增加,可逆贮氢容量为3.0%H2。
The Mg2Ni- 1.00 % Pd (mass fraction) alloy was prepared by mechanical alloying. XRD and AFM analyses were used to identify the phase and microstructure of the Mg2Ni-1.00% Pd alloy before and after hydrogen absorption. Kinetics curves and PCT curves of Mg2Ni-1.00% Pd-H2 system were measured. The results showed that the particle size of MgaNi-1.00% Pd alloy prepared by mechanical milling is between 10 ~ 50 nm. Ball milling with 1.00%Pd could significantly improve the hydriding/dehydriding (H/D) performance of nanocrystalline Mg2Ni. Comparing with the Mg2Ni alloy prepared by melting, the sample could easily absorb hydrogen at 423 and 473 K under the initial hydrogen pressure of 1.17 MPa without activation. There was obvious and long-width plateaus on the PCT curves, the hysteresis effect existed during hydrogen absorption/desorption and it decreased with the increase of temperature. Comparing with the Mg2Ni alloy prepared by melting, the enthalpy of nanocrystalline Mg2Ni-1.00% Pd decreased at hydrogen absorption and increased when hydrogen desorption. The nanocrystalline Mg2Ni-1. 00% Pd sample had a reversible storage capacity as high as 3.0%H2.
出处
《稀有金属》
EI
CAS
CSCD
北大核心
2007年第1期32-37,共6页
Chinese Journal of Rare Metals
基金
中国工程物理研究院基金资助项目(20040870)
关键词
贮氢合金
MG2NI
高能球磨
吸放氢性能
hydrogen storage alloy
Mg2Ni
high-energy-milling
hydriding and dehydriding properties