Sulfidation of nickel- and cobalt-promoted molybdenum-alumina catalysts using a radioisotope 35S-labeled H2S pulse tracer method

被引:19
作者
Qian, WH [1 ]
Ishihara, A [1 ]
Aoyama, Y [1 ]
Kabe, T [1 ]
机构
[1] Tokyo Univ Agr & Technol, Dept Appl Chem, Tokyo 1848588, Japan
关键词
sulfidation; nickel- and cobalt-promoted Mo/Al2O3 catalysts; S-35-radioisotope pulse tracer method;
D O I
10.1016/S0926-860X(99)00454-8
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 sulfidation state in a series of nickel- and cobalt-promoted Mo/Al2O3 catalysts was investigated using S-35 radioisotope pulse tracer methods (RPTM). Several pulses of S-35-labeled H2S ([S-35]H2S) were introduced into catalysts in a nitrogen stream until the radioactivity in the recovered pulse approached the radioactivity of the introduced pulse. From the amount of [S-35]H2S introduced, the amount of sulfur accumulated on the catalyst was estimated. The amounts of sulfur accumulated on the catalysts increased with increasing temperature for all catalysts and the cobalt-promoted catalysts showed features similar to those of the nickel-promoted catalysts. It was found that the sulfided states of the catalysts close to the stoichiometric states, where Ni, Co and Mo are present as NiS, Co9S8 and MoS2, was attained at 400 degrees C for all catalysts. Moreover, it was suggested that only molybdenum was sulfided below 300 degrees C; the sulfidation of nickel oxide and cobalt oxide in the Ni- or the Co-Mo/Al2O3 catalyst is more difficult at lower temperatures and the sulfidation of nickel and cobalt species occurs only at higher temperatures (above 300 degrees C). (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:103 / 110
页数:8
相关论文
共 32 条
[1]   TEMPERATURE-PROGRAMMED SULFIDING OF MOO3/AL2O3 CATALYSTS [J].
ARNOLDY, P ;
VANDENHEIJKANT, JAM ;
DEBOK, GD ;
MOULIJN, JA .
JOURNAL OF CATALYSIS, 1985, 92 (01) :35-55
[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]   S-35 RADIOTRACER STUDIES OF THE EFFECT OF HYDROGEN-SULFIDE ON A MOLYBDENUM-DISULFIDE CATALYST IN THE HYDROGENATION OF BUTA-1,3-DIENE [J].
CAMPBELL, KC ;
MIRZA, ML ;
THOMSON, SJ ;
WEBB, G .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1984, 80 :1689-1704
[4]   THE STRUCTURE OF HIGHLY DISPERSED SIO2-SUPPORTED MOLYBDENUM OXIDE CATALYSTS DURING SULFIDATION [J].
DEBOER, M ;
VANDILLEN, AJ ;
KONINGSBERGER, DC ;
GEUS, JW .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (32) :7862-7870
[5]   Working surface science model of CoMoS hydrodesulfurization catalysts [J].
deJong, AM ;
deBeer, VHJS ;
vanVeen, JAR ;
Niemantsverdriet, JW .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A, 1997, 15 (03) :1592-1596
[6]   SULFIDATION MECHANISM OF MOLYBDENUM CATALYSTS SUPPORTED ON A SIO2/SI(100) MODEL SUPPORT STUDIED BY SURFACE SPECTROSCOPY [J].
DEJONG, AM ;
BORG, HJ ;
VANIJZENDOORN, LJ ;
SOUDANT, VGFM ;
DEBEER, VHJ ;
VANVEEN, JAR ;
NIEMANTSVERDRIET, JW .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (24) :6477-6483
[7]   Surface science model of a working cobalt-promoted molybdenum sulfide hydrodesulfurization catalyst: Characterization and reactivity [J].
deJong, AM ;
deBeer, VHJ ;
vanVeen, JAR ;
Niemantsverdriet, JW .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (45) :17722-17724
[8]   HIGH-RESOLUTION ELECTRON-MICROSCOPY OF HYDRODESULFURIZATION CATALYSTS - A REVIEW [J].
DELANNAY, F .
APPLIED CATALYSIS, 1985, 16 (02) :135-152
[9]   UPTAKE OF S-35 BY PD, IR, RU PROMOTED MO-OXIDE CATALYSTS AND THEIR ACTIVITY IN CYCLOHEXANOL TRANSFORMATION [J].
DOBROVOLSZKY, M ;
PAAL, Z ;
TETENYI, P .
CATALYSIS TODAY, 1991, 9 (1-2) :113-120
[10]   Uptake of hydrogen sulfide by molybdena-alumina catalysts containing group 8-10 metals [J].
Dobrovolszky, M ;
Paal, Z ;
Tetenyi, P .
APPLIED CATALYSIS A-GENERAL, 1996, 142 (01) :159-174