首页 | 本学科首页   官方微博 | 高级检索  
     检索      

Ni基催化剂上CH4、C2H6和C2H4的裂解积炭性能
引用本文:杨咏来,徐恒泳,李文钊.Ni基催化剂上CH4、C2H6和C2H4的裂解积炭性能[J].物理化学学报,2001,17(9):773-775.
作者姓名:杨咏来  徐恒泳  李文钊
作者单位:Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian 116023
基金项目:The Project Supported byNKBRSF (G1999022401)
摘    要:采用脉冲微反技术研究了添加半导体氧化物对Ni基催化剂上CH4、C2H6和C2H4的裂解积炭反应特性的影响。结果表明,n型半导体CeO2的添加降低了CH4和C2H6的积炭活性,而p型半导体Co3O4的添加则加速CH4和C2H6的裂解积炭;而对于与CH4和C2H6活化机制不同的C2H4分子的活化,上述影响机制正好相反,n型半导体CeO2的添加促进C2H4的裂解积炭反应,而p型半导体Co3O4的添加则抑制C2H4的裂解积炭反应。XPS分析表明,活性金属Ni与半导体氧化物之间存在的金属 半导体相互作用是这种影响机制的主要因素。

关 键 词:甲烷  乙烷  乙烯  镍催化剂  金属-半导体相互作用  
收稿时间:2001-05-25
修稿时间:2001年5月25日

Study on Carbon Deposition of CH4, C2H6 and C2H4 Cracking over Ni-based Catalysts
Abstract.Study on Carbon Deposition of CH4, C2H6 and C2H4 Cracking over Ni-based Catalysts[J].Acta Physico-Chimica Sinica,2001,17(9):773-775.
Authors:Abstract
Institution:Dalian Institute of Chemical Physics,Chinese Academy of Sciences,Dalian 116023
Abstract:Influence of the additions of different type semiconductor oxides to Ni-based catalyst on the characteristics of carbon deposition of CH_4,C_2H_6 and C_2H_4 cracking was studied by using pulse microreaction technique.It was discovered that,the addition of n-type semiconductor CeO_2 to Ni catalyst would decrease carbon deposition activity of CH4 and C_2H_6 cracking,whereas the addition of p-type semiconductor Co_3O_4 would increase carbon deposition activity of CH_4 and C_2H_6 cracking.On the other hand,the effect of semiconductor oxide additives on the characteristics of carbon deposition of C_2H_4 cracking is opposite to that of CH_4 and C_2H_6 due to the different activated mechanism.XPS results reveal that there is a metal-semiconductor interaction (MScI) between active metal Ni and semiconductor oxide,which is the most important factor leads to the above phenomenon.
Keywords:Methane  Ethane  Ethylene  Nickel catalyst  Metal-semiconductor interaction
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《物理化学学报》浏览原始摘要信息
点击此处可从《物理化学学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号