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Differential scanning calorimetry (DSC)and synchrotron X-ray diffraction study of unmilled and milled LiBH4 : a partial release of hydrogen at moderate temperatures

机译:未研磨和研磨的LiBH4的差示扫描量热法(DSC)和同步​​加速器X射线衍射研究:在中等温度下氢的部分释放

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摘要

Abstract: A systematic investigation of phase transitions in unmilled and milled LiBH4 has been performed by Pressurized Differential Scanning Calorimetry (PDSC). It was found that a large exotherm is present below the low temperature (LT) → high temperature (HT) phase transition. This exotherm is not caused by air contamination but seems to originate from hydrogen release from a solid solution in the matrix of LiBH4 low temperature phase. The exotherm activation energy has been measured to be 100 kJ mol–1. Calorimetric measurements under argon and hydrogen have shown that for the milled sample, the endothermic peak of the LT → HT transition is split in two when the PDSC scan is performed under hydrogen atmosphere. Synchrotron X-ray powder diffraction on the milled LiBH4 sample revealed only a single-step transition from the LT to HT phase, both under vacuum and under 2 and 40 bar of hydrogen pressure. The axial ratios for the LT LiBH4 below 300 K are significantly altered by milling; they are also considerably different under 40 bar of hydrogen, indicating an interaction between the hydrogen gas and the LT LiBH4 solid phase.
机译:摘要:已通过加压差示扫描量热法(PDSC)对未研磨和研磨的LiBH4中的相变进行了系统的研究。发现在低温(LT)→高温(HT)相变以下存在大的放热。该放热不是由空气污染引起的,而是似乎源于LiBH4低温相基质中固溶体释放的氢。据测量,放热活化能为100 kJ mol-1。在氩气和氢气下的量热测量表明,对于研磨后的样品,当在氢气气氛下进行PDSC扫描时,LT→HT跃迁的吸热峰被分成两部分。研磨后的LiBH4样品上的同步加速器X射线粉末衍射表明,在真空中以及在2 bar和40 bar的氢气压力下,从LT相到HT相只有一步过渡。低于300 K的LT LiBH4的轴向比会通过铣削显着改变;在40 bar氢气下,它们也有很大不同,表明氢气与LT LiBH4固相之间存在相互作用。

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