Highly stable Pd/CeO2 catalyst for hydrodechlorination of chlorobenzene

被引:80
作者
Gopinath, R
Lingaiah, N
Sreedhar, B
Suryanarayana, I
Prasad, PSS [1 ]
Obuchi, A
机构
[1] Indian Inst Chem Technol, Dept Phys & Inorgan Chem, Hyderabad 500007, Andhra Pradesh, India
[2] AIST, Inst Environm Management Technol, Catalyt & Electrochem Purificat Grp, Tsukuba, Ibaraki 3058569, Japan
关键词
hydrodechlorination; chlorobenzene; deposition-precipitation method; ceria-supported Pd catalysts;
D O I
10.1016/S0926-3373(03)00321-7
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
Catalysts containing 1 wt.% Pd supported on CeO2 were prepared by the deposition-precipitation (DP) and conventional impregnation (IMP) methods. The effect of the nature of precursor was also investigated using the chloride and nitrate salts of Pd. The catalysts were characterized by nitrogen adsorption (for BET surface area), CO chemisorption, temperature programmed reduction (TPR) and X-ray photoelectron spectroscopy (XPS). Their activity and stability was evaluated in the vapor phase hydrodechlorination (HDC) of chlorobenzene, using molecular hydrogen. The catalyst prepared by the DP method using the chloride precursor exhibited the highest stability during the reaction. Contrary to the general observation that the low dispersed catalysts are preferred for the HDC, by adopting the DP method of catalyst preparation, the present investigation demonstrates that high dispersed catalysts also offer better stability. This is a significant observation in terms of considerable reduction in Pd content of the catalyst. The higher stability is ascribed to the formation of cationic Pd species which resist deactivation. On the contrary, the IMP catalysts are susceptible for transformation into inactive palladium chloride, thus loosing stability. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:587 / 594
页数:8
相关论文
共 24 条
[1]   Influence of the reaction conditions and catalytic properties on the liquid-phase hydrodechlorination of chlorobenzene over palladium-supported catalysts:: Activity and deactivation [J].
Aramendía, MA ;
Boráu, V ;
García, IM ;
Jiménez, C ;
Lafont, F ;
Marinas, A ;
Marinas, JM ;
Urbano, FJ .
JOURNAL OF CATALYSIS, 1999, 187 (02) :392-399
[2]   Microwave heating during catalyst preparation: influence on the hydrodechlorination activity of alumina-supported palladium-iron bimetallic catalysts [J].
Berry, FJ ;
Smart, LE ;
Prasad, PSS ;
Lingaiah, N ;
Rao, PK .
APPLIED CATALYSIS A-GENERAL, 2000, 204 (02) :191-201
[3]   CHEMICAL STATE AND REACTIVITY OF SUPPORTED PALLADIUM .1. CHARACTERIZATION BY XPS AND UV-VISIBLE SPECTROSCOPY [J].
BOZONVERDURAZ, F ;
OMAR, A ;
ESCARD, J ;
PONTVIANNE, B .
JOURNAL OF CATALYSIS, 1978, 53 (01) :126-134
[4]  
Briggs D., 1990, AUGER XRAY PHOTOELEC, V1
[5]   TEMPERATURE-PROGRAMMED REDUCTION AND TEMPERATURE-RESOLVED SORPTION STUDIES OF STRONG METAL SUPPORT INTERACTION IN SUPPORTED PALLADIUM CATALYSTS [J].
CHANG, TC ;
CHEN, JJ ;
YEH, CT .
JOURNAL OF CATALYSIS, 1985, 96 (01) :51-57
[6]  
CHASTAIN J, 1992, HDB XRAY PHOTO ELECT
[7]   CONVERSION UNDER HYDROGEN OF DICHLORODIFLUOROMETHANE OVER BIMETALLIC PALLADIUM CATALYSTS [J].
COQ, B ;
HUB, S ;
FIGUERAS, F ;
TOURNIGANT, D .
APPLIED CATALYSIS A-GENERAL, 1993, 101 (01) :41-50
[8]   CONVERSION OF CHLOROBENZENE OVER PALLADIUM AND RHODIUM CATALYSTS OF WIDELY VARYING DISPERSION [J].
COQ, B ;
FERRAT, G ;
FIGUERAS, F .
JOURNAL OF CATALYSIS, 1986, 101 (02) :434-445
[9]   Ceria lattice oxygen ion substitution by Cl- during the reduction of Rh(Cl)/CeO2 catalysts.: Formation and stability of CeOCl [J].
Fajardie, F ;
Tempere, JF ;
Manoli, JM ;
Djega-Mariadassou, G ;
Blanchard, G .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1998, 94 (24) :3727-3735
[10]   HYDROGENOLYSIS OF METHYL-CHLORIDE ON METALS [J].
FUNG, SC ;
SINFELT, JH .
JOURNAL OF CATALYSIS, 1987, 103 (01) :220-223