...
首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Influences of calcination and reduction methods on the preparation of Ni2P/SiO2 and its hydrodenitrogenation performance
【24h】

Influences of calcination and reduction methods on the preparation of Ni2P/SiO2 and its hydrodenitrogenation performance

机译:煅烧和还原方法对Ni2P / SiO2的制备及其加氢脱氮性能的影响

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The SiO2 supported Ni2P catalysts were prepared by H-2 temperature-programmed reduction (TPR) or plasma reduction (PR) of two precursors, which were obtained by co-impregnation of SiO2 with (NH4)(2)HPO4 and Ni(NO3)(2)center dot 6H(2)O with and without calcination. Their catalytic performances were evaluated by the hydrodenitrogenation of quinoline. The catalysts prepared by the TPR method showed a higher denitrogenation activity at low temperature (<= 320 degrees C) but a lower denitrogenation activity at high temperature (>= 340 degrees C) relative to those prepared by the PR method. The results of CO chemisorption and XPS analysis suggest that this can be explained that more metallic Ni species were present in the surface of the catalysts prepared by the TPR method, which enhanced their hydrogenation activity at temperatures below 340 degrees C. Calcination of the precursor is not necessary for the preparation of Ni2P/SiO2. However, both the dispersion and the surface composition of the Ni2P phase were affected by the calcination and reduction approaches. (C) 2015 Elsevier B.V. All rights reserved.
机译:SiO2负载的Ni2P催化剂是通过两种前体的H-2程序升温还原(TPR)或等离子还原(PR)制备的,这是通过将SiO2与(NH4)(2)HPO4和Ni(NO3)共浸渍获得的(2)有和没有煅烧的中心点6H(2)O。它们的催化性能通过喹啉的加氢脱氮来评估。与通过PR方法制备的催化剂相比,通过TPR方法制备的催化剂在低温(<= 320℃)下显示出较高的脱氮活性,但是在高温(> = 340℃)下具有较低的脱氮活性。 CO化学吸附和XPS分析的结果表明,这可以解释为,通过TPR方法制备的催化剂表面存在更多的金属Ni物种,这增强了它们在340℃以下的温度下的氢化活性。无需制备Ni2P / SiO2。但是,Ni2P相的分散性和表面组成均受煅烧和还原方法的影响。 (C)2015 Elsevier B.V.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