中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Effect of Ethane Addition on Methane Dehydroaromatization over Mo/HZSM-5 Catalyst

文献类型:期刊论文

作者Sun Changyong1,2; Yao Songdong1; Shen Wenjie1; Lin Liwu1
刊名chinese journal of catalysis
出版日期2010
卷号31期号:1页码:78-83
关键词methane ethane dehydroaromatization molybdenum HZSM-5 zeolite
英文摘要the effect of ethane addition on methane dehydroaromatization over a mo/hzsm-5 catalyst was investigated. it was revealed that the ethane addition could not promote the conversion of methane but produced methane and increased coke deposition rate, causing rapid deactivation of the catalyst. however, ethane accelerated the formation of mo active centers (mo(2)c and/or moo(x)c(y) species), shortening the induction period and moving the benzene formation forward.
WOS标题词science & technology ; physical sciences ; technology
类目[WOS]chemistry, applied ; chemistry, physical ; engineering, chemical
研究领域[WOS]chemistry ; engineering
关键词[WOS]temperature nonoxidative activation ; galloaluminosilicate mfi zeolite ; co-reactant ; dehydro-aromatization ; zn-zsm-11 zeolite ; membrane reactor ; conversion ; transformation ; hydrocarbons ; mo/zsm-5
收录类别SCI
语种英语
WOS记录号WOS:000274753100014
公开日期2015-11-17
源URL[http://159.226.238.44/handle/321008/142011]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Liaoning, Peoples R China
2.Shantou Univ, Dept Chem, Shantou 515063, Guangdong, Peoples R China
推荐引用方式
GB/T 7714
Sun Changyong,Yao Songdong,Shen Wenjie,et al. Effect of Ethane Addition on Methane Dehydroaromatization over Mo/HZSM-5 Catalyst[J]. chinese journal of catalysis,2010,31(1):78-83.
APA Sun Changyong,Yao Songdong,Shen Wenjie,&Lin Liwu.(2010).Effect of Ethane Addition on Methane Dehydroaromatization over Mo/HZSM-5 Catalyst.chinese journal of catalysis,31(1),78-83.
MLA Sun Changyong,et al."Effect of Ethane Addition on Methane Dehydroaromatization over Mo/HZSM-5 Catalyst".chinese journal of catalysis 31.1(2010):78-83.

入库方式: OAI收割

来源:大连化学物理研究所

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