首页> 外文期刊>International journal of hydrogen energy >Copper-iron mixed oxide catalyst precursors prepared by glycine-nitrate combustion method for ammonia borane dehydrogenation processes
【24h】

Copper-iron mixed oxide catalyst precursors prepared by glycine-nitrate combustion method for ammonia borane dehydrogenation processes

机译:甘氨酸硝酸盐燃烧法制备的铜铁混合氧化物催化剂前驱体用于氨硼烷脱氢工艺

获取原文
获取原文并翻译 | 示例
       

摘要

The influence of the properties of copper ferrite, prepared by the combustion method from glycine-nitrate precursor, on the kinetics of NH3BH3 hydrolysis, thermolysis and hydrothermolysis are presented. As-prepared and annealed samples were studied by X-ray diffraction, scanning electron microscopy, differential dissolution, and attenuated total reflection infrared spectroscopy. It has been shown that in the hydrolysis and hydrothermolysis of NH3BH3, the as-prepared combustion product, which mainly consisted of a cubic spinel Cu0.67Fe2.33O4 with Fe2+ higher content, had the highest activity, as compared with oxides of copper and iron and the annealed samples. According to transmission electron microscopy and X-ray diffraction, in the reaction medium copper ferrite is reduced to nanosized Cu-0 and Fe-0. This allowed the average rate of H-2 evolution per 1 g of the composition to be increased from 30 to 76 ml.min(-1), as compared with non-catalytic process. The high gravimetric hydrogen capacity (7.3 wt%) was observed at 90 degrees C. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:提出了硝酸甘氨酸硝酸盐前驱体燃烧法制备的铁氧体铜性能对NH3BH3水解,热解和水热解动力学的影响。通过X射线衍射,扫描电子显微镜,微分溶解和衰减全反射红外光谱研究制备和退火的样品。结果表明,在NH3BH3的水解和水热解中,与铜和铁的氧化物相比,以Fe2 +含量更高的立方尖晶石Cu0.67Fe2.33O4组成的燃烧产物具有最高的活性。和退火样品。根据透射电子显微镜和X射线衍射,在反应介质中铜铁氧体被还原成纳米级的Cu-0和Fe-0。与非催化过程相比,这使得每1克组合物中H-2的平均析出速率从30 ml.min(-1)增加到76 ml.min(-1)。在90摄氏度下观察到高重量氢容量(7.3 wt%)。(C)2019 Hydrogen Energy Publications LLC。由Elsevier Ltd.出版。保留所有权利。

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