首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >A study on CO2 and CH4 conversion to synthesis gas and higher hydrocarbons by the combination of catalysts and dielectric-barrier discharges
【24h】

A study on CO2 and CH4 conversion to synthesis gas and higher hydrocarbons by the combination of catalysts and dielectric-barrier discharges

机译:催化剂与介电势垒放电结合将CO2和CH4转化为合成气和高级烃的研究

获取原文
获取原文并翻译 | 示例
           

摘要

The conversion of CH4 and CO2 to synthesis gas (H-2 + CO) and higher hydrocarbons was investigated over BaTiO3, glass, Ni/SiO2, NiFe/SiO2, and a mixture of Ni/SiO2 and BaTiO3 in dielectric-barrier discharges (DBDs) at low temperatures and ambient pressure. The fresh and spent Ni/SiO2 catalyst samples were characterized by SEM, XRD, BET and TEM. The variation of the permittivity of packing materials with the same size did not influence the reaction significantly. Exposing one metal electrode to plasma could enhance the selectivity to CO in the reaction. The conversion of CO2 and CH4 decreased in the sequence of BaTiO3 > NiFe/SiO2> Ni/SiO2. A NiFe/SiO2 catalyst increased the selectivity to H-2, and both Ni/SiO2 and NiFe/SiO2 catalysts enhanced the selectivity to CO in the reaction. A reaction mechanism of plasma assisted CO2 and CH4 conversion was proposed. Specific input energy (SIE) was an important factor affecting the reaction, and it was possible to alter the product selectivity by optimizing the residence time at a certain SIE over a Ni/SiO2 catalyst. (C) 2015 Elsevier B.V. All rights reserved.
机译:在介电势垒放电(DBDs)中研究了BaTiO3,玻璃,Ni / SiO2,NiFe / SiO2以及Ni / SiO2和BaTiO3的混合物上CH4和CO2向合成气(H-2 + CO)和高级烃的转化)在低温和环境压力下。用SEM,XRD,BET和TEM对新鲜和废Ni / SiO2催化剂样品进行表征。相同尺寸的包装材料的介电常数的变化不会显着影响反应。将一个金属电极暴露于等离子体可以提高反应中对CO的选择性。按BaTiO3> NiFe / SiO2> Ni / SiO2的顺序,CO2和CH4的转化率降低。 NiFe / SiO2催化剂增加了对H-2的选择性,Ni / SiO2和NiFe / SiO2催化剂均增加了对CO的选择性。提出了等离子体辅助CO2和CH4转化的反应机理。比输入能量(SIE)是影响反应的重要因素,并且可以通过优化在特定SIE上在Ni / SiO 2催化剂上的停留时间来改变产物选择性。 (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