NiMoS/γ-Al2O3 catalysts:: The nature and the aging behavior of active sites in HDN reactions

被引:42
作者
Zhang, LP [1 ]
Karakas, G [1 ]
Ozkan, US [1 ]
机构
[1] Ohio State Univ, Dept Chem Engn, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
active sites; aging; supported NiMo sulfide; TPD; TPR; XPS; SEM; hydrodenitrogenation; indole; H2S;
D O I
10.1006/jcat.1998.2160
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 work presented in this paper is a continuation of our earlier work aimed at acquiring a fundamental understanding of sulfided Ni-Mo/gamma-Al2O3 catalysts in HDN catalysis, A series of temperature-programmed desorption and reduction experiments were performed over in-situ sulfided bare gamma-alumina support, alumina-supported monometallic Ni, Mo, and bimetallic NiMo catalysts. The TPD and TPR results were linked to the active site assignment of Ni- and Mo-associated centers in HDN reactions. Postreaction XPS and SEM characterizations were performed for catalysts used in HDN for up to 1000 h. One of the major changes during the aging of the Ni-Mo/gamma-Al2O3 catalysts was the loss of some active sites associated with the Ni promoters, The decreased Ni content over the catalyst surface was consistent with the observed decrease in the hydrogenation function of the catalyst. Two possible mechanisms are suggested for the loss of Ni active sites, One is coking that spreads from the alumina support to the nickel sites. Another is segregation of some Ni atoms from the Ni-Mo-S structure due to loss of structural sulfur, (C) 1998 Academic Press.
引用
收藏
页码:457 / 465
页数:9
相关论文
共 35 条
[21]  
Satterfield C.N., 1991, HETEROGENEOUS CATALY, P383
[22]   H-2 interaction with S atoms of a MoS2 modelled catalytic site: Electronic density analysis for S-H formation [J].
Sierraalta, A ;
Ruette, F .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 1996, 109 (03) :227-238
[23]   RECENT BASIC RESEARCH IN HYDRODESULFURIZATION CATALYSIS [J].
TOPSOE, H ;
CLAUSEN, BS ;
TOPSOE, NY ;
PEDERSEN, E .
INDUSTRIAL & ENGINEERING CHEMISTRY FUNDAMENTALS, 1986, 25 (01) :25-36
[24]   INSITU MOSSBAUER EMISSION-SPECTROSCOPY STUDIES OF UNSUPPORTED AND SUPPORTED SULFIDED CO-MO HYDRODESULFURIZATION CATALYSTS - EVIDENCE FOR AND NATURE OF A CO-MO-S PHASE [J].
TOPSOE, H ;
CLAUSEN, BS ;
CANDIA, R ;
WIVEL, C ;
MORUP, S .
JOURNAL OF CATALYSIS, 1981, 68 (02) :433-452
[25]   IMPORTANCE OF CO-MO-S TYPE STRUCTURES IN HYDRODESULFURIZATION [J].
TOPSOE, H ;
CLAUSEN, BS .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1984, 26 (3-4) :395-420
[26]  
TopsOe H, 1996, HYDROTREATING CATALY
[27]   CHARACTERIZATION OF THE STRUCTURES AND ACTIVE-SITES IN SULFIDED CO-MO/AL2O3 AND NI-MO/AL2O3 CATALYSTS BY NO CHEMISORPTION [J].
TOPSOE, NY ;
TOPSOE, H .
JOURNAL OF CATALYSIS, 1983, 84 (02) :386-401
[28]   A MODEL OF COKE ON HYDROTREATING CATALYSTS UNDER REACTION CONDITIONS [J].
VANDOORN, J ;
MOULIJN, JA .
FUEL PROCESSING TECHNOLOGY, 1993, 35 (03) :275-287
[29]   ON THE CATALYTIC SIGNIFICANCE OF A CO-MO-S PHASE IN CO-MO-AL2O3 HYDRODESULFURIZATION CATALYSTS - COMBINED INSITU MOSSBAUER EMISSION-SPECTROSCOPY AND ACTIVITY STUDIES [J].
WIVEL, C ;
CANDIA, R ;
CLAUSEN, BS ;
MORUP, S ;
TOPSOE, H .
JOURNAL OF CATALYSIS, 1981, 68 (02) :453-463
[30]   CATALYTIC HYDRODENITROGENATION OF QUINOLINE IN A TRICKLE-BED REACTOR - EFFECT OF HYDROGEN-SULFIDE [J].
YANG, SH ;
SATTERFIELD, CN .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1984, 23 (01) :20-25