A kinetic study of methanol decomposition catalyzed over plate-type palladium catalyst

被引:0
作者
Shinji Shiizaki
Ikuo Nagashima
Yasuyuki Matsumura
Masatake Haruta
机构
[1] Akashi Technical Institute,Kawasaki Heavy Industries, Ltd.
[2] Osaka National Research Institute,AIST
来源
Catalysis Letters | 1998年 / 56卷
关键词
reaction rate; reaction mechanism; methanol decomposition; palladium;
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摘要
A kinetic study of the catalytic methanol decomposition to carbon monoxide and hydrogen has been carried out in the pressure range of methanol up to 8 atm at 200 and 250°C over a palladium catalyst supported on an oxidized aluminum plate. The reaction pathway can be proposed as (i) dissociative adsorption of methanol to methoxyl groups and hydrogen adsorbed on palladium sites, (ii) decomposition of the methoxyl groups to carbon monoxide and hydrogen adsorbed, and (iii) desorption of the surface carbon monoxide and hydrogen species. It is suggested that the second step is rate-determining and the surface hydrogen species enhance the decomposition of the methoxyl groups.
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页码:227 / 230
页数:3
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共 47 条
[1]  
Fox J.M.(1993)undefined Catal. Rev. Sci. Eng. 35 169-undefined
[2]  
Murata K.(1996)undefined Int. J. Hydrogen Energy 21 201-undefined
[3]  
Yamamoto K.(1991)undefined Chem. Eng. 36 42-undefined
[4]  
Kameyama H.(1981)undefined J. Jpn. Petrol. Inst. 24 322-undefined
[5]  
Kameyama H.(1990)undefined Bul. Chem. Soc. Jpn. 63 108-undefined
[6]  
Inoue M.(1991)undefined J. Catal. 128 198-undefined
[7]  
Yamanaka R.(1995)undefined Kagaku Kogaku Ronbunshu 21 1002-undefined
[8]  
Murata K.(1997)undefined Catal. Lett. 44 189-undefined
[9]  
Niiyama H.(1982)undefined J. Chem. Phys. 76 6308-undefined
[10]  
Tamai S.(1983)undefined Surf. Sci. 135 65-undefined