El-Eskandarany Mohamed Sherif
Nanotechnology and Advanced Materials Program, Energy and Building Research Center, Kuwait Institute for Scientific Research Safat 13109 Kuwait
RSC Adv. 2019 Jan 9;9(2):1036-1046. doi: 10.1039/c8ra08200f. eCollection 2019 Jan 2.
Because of its high thermal stability and poor hydrogenation/dehydrogenation kinetics, magnesium hydride (MgH) requires mechanical treatment and/or doping with catalytic agents(s) to understand the decomposition temperature and accelerate the gas uptake/release kinetics. Whereas all catalytic species used for this purpose are crystalline materials, in this paper use of titanium nickel (TiNi) metallic glassy (MG) nanopowders for enhancing the hydrogenation/dehydrogenation kinetics behavior of MgH powders is reported. In the present research, MG-TiNi ribbons, prepared using a melt spinning technique were snipped into small pieces and then cryo-milled under a flow of liquid nitrogen to obtain submicron-powders (500 nm). The as-prepared MgH powders were doped with 10 wt% of the glassy powder and then cryo-milled for 25 h. The structural and morphological analysis indicated that the cryo-milling process succeeded in maintaining the short-range order structure of MG-TiNi, and in reducing the MgH grain size to the nanolevel. The results showed that the as-prepared nanocomposite powders obtained after 25 h of cryo-milling decomposed at 283 °C, with an apparent activation energy of 87.3 kJ mol. The MgH/10 wt% MG-TiNi nanocomposite powders were cold rolled into thin strips, using a cold rolling technique. These cold rolled strips possessed excellent morphological characteristics, shown by the homogeneous distribution of the MgH spherical particles (10 nm in diameter) in the glassy TiNi matrix. Furthermore, the hydrogenation/dehydrogenation kinetics measured at 225 °C were very fast, as indicated by the short time (400 s) required to uptake/release 5.7 wt% H. At this temperature, the system possessed good life-time cycling performance - achieving 84 continuous cycles within 30 h without failure or degradation.
由于氢化镁(MgH)具有高热稳定性以及较差的氢化/脱氢动力学性能,因此需要进行机械处理和/或用催化剂进行掺杂,以降低其分解温度并加快气体吸收/释放动力学。尽管用于此目的的所有催化物质均为晶体材料,但本文报道了使用钛镍(TiNi)金属玻璃(MG)纳米粉末来增强MgH粉末的氢化/脱氢动力学行为。在本研究中,将采用熔体纺丝技术制备的MG-TiNi薄带剪成小块,然后在液氮流中进行低温球磨以获得亚微米粉末(500纳米)。将制备好的MgH粉末与10 wt%的玻璃态粉末掺杂,然后低温球磨25小时。结构和形态分析表明,低温球磨过程成功地保持了MG-TiNi的短程有序结构,并将MgH的晶粒尺寸减小到纳米级。结果表明,经过25小时低温球磨后制备的纳米复合粉末在283°C下分解,表观活化能为87.3 kJ/mol。采用冷轧技术将MgH/10 wt% MG-TiNi纳米复合粉末冷轧成薄带。这些冷轧薄带具有优异的形态特征,MgH球形颗粒(直径10纳米)在玻璃态TiNi基体中均匀分布。此外,在225°C下测得的氢化/脱氢动力学非常快,吸收/释放5.7 wt% H所需的时间很短(400秒)。在此温度下,该体系具有良好的寿命循环性能,在30小时内实现了84次连续循环而无故障或降解。