M. Dilixiati, Kazuyuki Kanda, K. Ishikawa, K. Aoki
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引用次数: 10
摘要
采用压差扫描量热仪(PDSC)、粉末x射线衍射仪(XRD)、差示扫描量热仪(DSC)和氢分析仪研究了c15 Laves相TbFe 2在氢气气氛中加热时结构变化的压力依赖性。在0.5 MPa H以上,随着温度的升高,晶态吸氢、氢致非晶化(HIA)、tbh2的析出和剩余非晶态合金分解为α-Fe和tbh2的过程均发生放热,与升温速率无关。在0.2 MPa H 2 (0.33 K/s)和0.1 MPa H 2 (0.17 K/s)条件下,HIA和tbh2降水同时发生。而在0.1 MPa H 2 (0.33 K/s)下,吸附氢的c- tbfe2h 3.5晶体直接分解为α-Fe和tbh2。即在较低的氢压力和较高的加热速率下,未形成非晶态相。根据结晶态或tfe2中吸收的氢含量,讨论了在临界氢压力以上和临界加热速率以下发生HIA的原因。
Pressure dependence of hydrogen-induced amorphization in C15 Laves phase TbFe2 : Special issue on hydrogen absorbing materials
The pressure dependence of structural changes of C 15 Laves phase TbFe 2 heated in a hydrogen atmosphere was investigated using a pressure differential scanning calorimeter (PDSC), a powder X-ray diffractometer (XRD), a differential scanning calorimeter (DSC) and a hydrogen analyzer. Hydrogen absorption in the crystalline state, hydrogen-induced amorphization (HIA), precipitation of TbH 2 and decomposition of the remaining amorphous alloy into α-Fe and TbH 2 occurred exothermally with increasing temperature above 0.5 MPa H 2 , independent of the heating rate. HIA and precipitation of TbH 2 occurred simultaneously in 0.2 MPa H 2 (0.33 K/s) and in 0.1 MPa H 2 (0.17 K/s). On the contrary, hydrogen absorbed crystalline c-TbFe 2 H 3.5 decomposed directly into α-Fe and TbH 2 in 0.1 MPa H 2 (0.33 K/s). That is, no amorphous phase was formed at the lower hydrogen pressure and at a high heating rate. The reason why HIA occurs above, the critical hydrogen pressure and below the critical heating rate was discussed on the basis of the hydrogen content absorbed in the crystalline state or TbFe 2 .