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Kinetic- and thermodynamic-based improvements of lithium borohydride incorporated into activated carbon

机译:基于动力学和热力学的硼氢化锂在活性炭中的改进

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摘要

LiBH_4 was incorporated into an activated carbon (AC) scaffold using a chemical impregnation method. Confinement of LiBH_4 within the carbon nanopores was found to significantly improve both the hydrogen sorption kinetics and thermodynamics, compared to the bulk hydride. The LiBH_4/AC sample starts to release hydrogen from just 220 deg C, which is 150 deg C lower than the onset dehydrogenation temperature of bulk LiBH_4. The dehydrogenation rate of the LiBH_4/AC sample was one order of magnitude faster than that of bulk LiBH_4. The temperature and hydrogen pressure conditions required for restoring the hydride were also significantly reduced when LiBH_4 was incorporated into AC. Preliminary study showed that the dissociation hydrogen pressure of LiBH_4 could be enhanced by around one order of magnitude upon incorporating the hydride into AC. X-ray diffraction, Fourier transform infrared spectroscopy and nitrogen adsorption analyses were used to confirm the nanostructure of LiBH_4 in the AC scaffold.
机译:使用化学浸渍方法将LiBH_4掺入活性炭 (AC) 支架中。与本体氢化物相比,将LiBH_4限制在碳纳米孔内可显着改善氢吸附动力学和热力学。LiBH_4/AC 样品从仅 220 摄氏度开始释放氢气,比散装LiBH_4的起始脱氢温度低 150 摄氏度。LiBH_4/AC样品的脱氢速率比散装LiBH_4快一个数量级。当LiBH_4掺入AC中时,恢复氢化物所需的温度和氢气压力条件也显著降低。 初步研究表明,将氢化物掺入AC后,LiBH_4的解离氢压力可提高约一个数量级。 采用X射线衍射、傅里叶变换红外光谱和氮气吸附分析证实了AC支架中LiBH_4的纳米结构。

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