HYDRODESULFURIZATION OF DIBENZOTHIOPHENE ON ALUMINA-SUPPORTED MOLYBDENUM NITRIDE

被引:132
作者
NAGAI, M
MIYAO, T
TUBOI, T
机构
[1] Department of Chemical Engineering, Tokyo University of Agriculture and Technology, Tokyo, 184, Koganei
关键词
HDS; DIBENZOTHIOPHENE; MOLYBDENUM NITRIDE; HIGH SELECTIVITY;
D O I
10.1007/BF00769493
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An alumina-supported molybdenum nitrided catalyst was prepared and tested to determine its activity and selectivity during the hydrodesulfurization of dibenzothiophene. The nitrided catalyst was extremely active for the selective C-S bond breakage of dibenzothiophene to produce biphenyl.
引用
收藏
页码:9 / 14
页数:6
相关论文
共 8 条
[1]  
HADDIX GW, 1987, J PHYS CHEM-US, V93, P5859
[2]   CATALYTIC HYDRODESULFURIZATION BY MOLYBDENUM NITRIDE [J].
MARKEL, EJ ;
VANZEE, JW .
JOURNAL OF CATALYSIS, 1990, 126 (02) :643-657
[3]   POISONING EFFECT OF NITROGEN-COMPOUNDS ON DIBENZOTHIOPHENE HYDRODESULFURIZATION ON SULFIDED NIMO/AL2O3 CATALYSTS AND RELATION TO GAS-PHASE BASICITY [J].
NAGAI, M ;
SATO, T ;
AIBA, A .
JOURNAL OF CATALYSIS, 1986, 97 (01) :52-58
[4]   CATALYSIS OVER MOLYBDENUM CARBIDES AND NITRIDES .1. CATALYST CHARACTERIZATION [J].
RANHOTRA, GS ;
HADDIX, GW ;
BELL, AT ;
REIMER, JA .
JOURNAL OF CATALYSIS, 1987, 108 (01) :24-39
[5]   CATALYSIS OVER MOLYBDENUM CARBIDES AND NITRIDES .2. STUDIES OF CO HYDROGENATION AND C2H6 HYDROGENOLYSIS [J].
RANHOTRA, GS ;
BELL, AT ;
REIMER, JA .
JOURNAL OF CATALYSIS, 1987, 108 (01) :40-49
[6]   CATALYTIC BEHAVIOR OF SELECTED TRANSITION-METAL CARBIDES, NITRIDES, AND BORIDES IN THE HYDRODENITROGENATION OF QUINOLINE [J].
SCHLATTER, JC ;
OYAMA, ST ;
METCALFE, JE ;
LAMBERT, JM .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1988, 27 (09) :1648-1653
[7]   COMPOUNDS OF MOLYBDENUM AND TUNGSTEN WITH HIGH SPECIFIC SURFACE-AREA .1. NITRIDES [J].
VOLPE, L ;
BOUDART, M .
JOURNAL OF SOLID STATE CHEMISTRY, 1985, 59 (03) :332-347
[8]   AMMONIA-SYNTHESIS ON MOLYBDENUM NITRIDE [J].
VOLPE, L ;
BOUDART, M .
JOURNAL OF PHYSICAL CHEMISTRY, 1986, 90 (20) :4874-4877