...
首页> 外文期刊>Journal of Materials Science >A benign synthesis of alane by the composition-controlled mechanochemical reaction of sodium hydride and aluminum chloride
【24h】

A benign synthesis of alane by the composition-controlled mechanochemical reaction of sodium hydride and aluminum chloride

机译:氢化钠和氯化铝的组合控机械化学反应良性合成alane

获取原文
获取原文并翻译 | 示例

摘要

Solid-state mechanochemical synthesis of alane (AlH3) starting from sodium hydride (NaH) and aluminum chloride (AlCl3) has been achieved at room temperature. The transformation pathway of this solid-state reaction was controlled by a stepwise addition of AlCl3 to the initial reaction mixture that contained sodium hydride in excess of stoichiometric amount. As in the case of previously investigated LiH-AlCl3 system, complete selectivity was achieved whereby formation of unwanted elemental aluminum was fully suppressed, and AlH3 was obtained in quantitative yield. Reaction progress during each step was investigated by means of solid-state NMR and powder X-ray diffraction, which revealed that the overall reaction proceeds through a series of intermediate alanates that may be partially chlorinated. The NaH-AlCl3 system presents some subtle differences compared to LiH-AlCl3 system particularly with respect to optimal concentrations needed during one of the reaction stages. Based on the results, we postulate that high local concentrations of NaH may stabilize chlorine-containing derivatives and prevent decomposition into elemental aluminum with hydrogen evolution. Complete conversion with quantitative yield of alane was confirmed by both SSNMR and hydrogen desorption analysis.
机译:在室温下实现了从氢化钠(NAH)和氯化铝(ALCl3)开始的铝化合物(ALH3)的固态化学合成。该固态反应的转化途径通过逐步加入AlCl 3至初始反应混合物,其含有过量化学计量的氢化钠。如先前研究的LIH-ALCL3系统的情况下,实现了完全的选择性,从而完全抑制了不需要的元素铝的形成,并以定量产率获得alh3。通过固态NMR和粉末X射线衍射研究了每步的反应进展,这揭示了整个反应通过一系列可以部分氯化的中间体进行。与LIH-ALCL3系统相比,NaH-AlCl3系统特别是关于反应阶段之一期间所需的最佳浓度的微妙差异。基于结果,我们假设NaH的高局部浓度可能稳定含氯的衍生物并防止分解成具有氢气的元素铝。通过SSNMR和氢解吸分析证实了通过铝的定量产率的完全转化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号