STUDY OF HYDRODESULFURIZATION OF DIBENZOTHIOPHENE ON NI-MO/AL2O3, MO/AL2O3, AND NI/AL2O3 CATALYSTS BY THE USE OF RADIOISOTOPE S-35 TRACER

被引:59
作者
KABE, T
QIAN, WH
ISHIHARA, A
机构
[1] Department of Chemical Engineering, Tokyo University of Agriculture and Technology, Koganei, Tokyo 184, Nakamachi
关键词
D O I
10.1006/jcat.1994.1282
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
The radioisotope tracer method has been used to quantify the behavior of sulfur on sulfided Ni-Mo/Al2O3, Mo/Al2O3, and Ni/Al2O3. The apparent activation energies of HDS reaction for DBT for the three catalysts were 20 +/- 1 kcal/mol. The formation rate constants of S-35-H2S were determined and the amount of labile sulfur on the sulfided catalysts was estimated by tracing the changes in radioactivities of the unreacted S-35-DBT and the formed S-35-H2S during the HDS reaction of S-35-labeled dibenzothiophene (S-35-DBT). It was deduced that ca. 75% of sulfur in the sulfided Mo/Al2O3 was related to HDS reaction at infinite rate of HDS. Compared with the amounts of labile sulfur in the sulfided Ni-Mo/Al2O3, Mo/Al2O3, and Ni/Al2O3, it was determined that the amounts of labile sulfur were 1.6, 9.8, and 18.4 mg sulfur/g catalyst at 280 degrees C for the three catalysts, respectively. And it was suggested that the sulfur in the form of NiS on the sulfided Ni-Mo/Al2O3 was not labile and that the sulfurs attached to both Mo and Ni atom were more labile and related to HDS. The promotion of Ni for Mo-based catalysts was attributed to the sulfur bonded to both Mo and Ni in the MoS2 phase being more labile. (C) 1994 Academic Press, Inc.
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页码:171 / 180
页数:10
相关论文
共 35 条
[1]  
Alcock C.B., 1976, PRINCIPLES PYROMETAL
[2]   EXTENDED X-RAY ABSORPTION FINE-STRUCTURE DETERMINATION OF THE STRUCTURE OF COBALT IN CARBON-SUPPORTED CO AND CO-MO SULFIDE HYDRODESULFURIZATION CATALYSTS [J].
BOUWENS, SMAM ;
VANVEEN, JAR ;
KONINGSBERGER, DC ;
DEBEER, VHJ ;
PRINS, R .
JOURNAL OF PHYSICAL CHEMISTRY, 1991, 95 (01) :123-134
[3]   STRUCTURE OF THE MOLYBDENUM SULFIDE PHASE IN CARBON-SUPPORTED MO AND CO-MO SULFIDE CATALYSTS AS STUDIED BY EXTENDED X-RAY ABSORPTION FINE-STRUCTURE SPECTROSCOPY [J].
BOUWENS, SMAM ;
PRINS, R ;
DEBEER, VHJ ;
KONINGSBERGER, DC .
JOURNAL OF PHYSICAL CHEMISTRY, 1990, 94 (09) :3711-3718
[4]   METAL SULFIDE SUPPORT INTERACTIONS [J].
BURCH, R ;
COLLINS, A .
JOURNAL OF CATALYSIS, 1986, 97 (02) :385-389
[5]   FUNDAMENTAL-STUDIES OF TRANSITION-METAL SULFIDE HYDRODESULFURIZATION CATALYSTS [J].
CHIANELLI, RR .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1984, 26 (3-4) :361-393
[6]  
CLAUSEN BS, 1981, B SOC CHIM BELG, V90, P1249
[7]  
DELMON B, 1990, CATALYSTS PETROLEUM, P1
[8]   EFFECTS OF SOLVENTS ON DEEP HYDRODESULFURIZATION OF BENZOTHIOPHENE AND DIBENZOTHIOPHENE [J].
ISHIHARA, A ;
ITOH, T ;
HINO, T ;
NOMURA, M ;
QI, PY ;
KABE, T .
JOURNAL OF CATALYSIS, 1993, 140 (01) :184-189
[9]   DEEP DESULFURIZATION OF LIGHT OIL .3. EFFECTS OF SOLVENTS ON HYDRODESULFURIZATION OF DIBENZOTHIOPHENE [J].
ISHIHARA, A ;
KABE, T .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1993, 32 (04) :753-755
[10]   DEEP DESULFURIZATION OF LIGHT OIL .2. HYDRODESULFURIZATION OF DIBENZOTHIOPHENE, 4-METHYLDIBENZOTHIOPHENE AND 4,6-DIMETHYLDIBENZOTHIOPHENE [J].
KABE, T ;
ISHIHARA, A ;
ZHANG, Q .
APPLIED CATALYSIS A-GENERAL, 1993, 97 (01) :L1-L9