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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >Low temperature de/hydrogenation in the partially crystallized Mg60Ce10Ni20Cu10 metallic glasses induced by milling with process control agents
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Low temperature de/hydrogenation in the partially crystallized Mg60Ce10Ni20Cu10 metallic glasses induced by milling with process control agents

机译:通过研磨与过程控制剂诱导的部分结晶Mg60NE10NI20CU10金属玻璃中的低温除/氢化

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Slow hydrogen de/absorption kinetics and high hydrogen desorption temperature are still great challenges for both crystalline and amorphous Mg-based alloys. In this work, through using ethanol (E) and ethylene glycol (EG) as milling process control agents (PCAs), partial and controllable crystallization of the melt-spun Mg60Ce10Ni20Cu10 metallic glass was achieved. The microstructure of the as-milled powders and corresponding hydrides was characterized by DSC, SEM, TEM and XRD. De/hydrogenation properties were measured by automatic Sieverts-type apparatus and TG-MS. It was found that the PCAs could lead to partial crystallization of the Mg60Ce10Ni20Cu10 metallic glass due to the dissolving of oxygen into the amorphous structure from PCAs. The introduction of a small amount of the nanocrystals promoted greatly hydrogen de/absorption properties of the melt-spun Mg60Ce10Ni20Cu10 alloy. The hydrogenation temperature could be decreased to below 100 degrees C and the initial hydrogen desorption temperature of the EG-added hydride could be decreased to below 150 degrees C. The structure evolution of the de/hydrogenated samples of the EG-added powder was also studied. The hydrogen-induced crystallizationwas evidently observed in the hydrogenated sample. The ethanol and ethylene glycol was found to be effective milling PCAs to create a composite structure of amorphous and crystalline, and the composite structure greatly enhanced the de/hydrogenation properties. However, the structural stability and reversibility of such composite structure during hydrogenation were still great challenges. (C) 2019 Elsevier B.V. All rights reserved.
机译:慢性氢DE /吸收动力学和高氢解吸温度对于结晶和无定形Mg基合金仍然存在很大的挑战。在这项工作中,通过使用乙醇(E)和乙二醇(例如)作为研磨过程控制剂(PCA),实现熔融纺丝Mg60CE10Cu1010101010101010金属玻璃的部分和可控结晶。通过DSC,SEM,TEM和XRD表征了AS-MICHED粉末和相应氢化物的微观结构。通过自动SIEVERTS型装置和TG-MS测量去/氢化性能。发现PCA可以导致Mg60CE10Ni20Cu10金属玻璃的部分结晶,由于氧气溶解到来自PCA的无定形结构中。少量纳米晶体的引入促进了熔融纺丝Mg60CE10Cu20Cu10型合金的大大氢去/吸收性能。氢化温度可以降低至低于100℃,并且例如加入氢化物的初始氢解吸温度降至150℃以下。还研究了例如加入粉末的DE /氢化样品的结构演变。在氢化样品中明显地观察到氢诱导的结晶。发现乙醇和乙二醇是有效研磨的PCA,以产生无定形和结晶的复合结构,并且复合结构大大提高了DE /氢化性能。然而,在氢化过程中这种复合结构的结构稳定性和可逆性仍然存在巨大的挑战。 (c)2019 Elsevier B.v.保留所有权利。

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