KINETICS AND ISOTOPE EFFECT OF AMMONIA SYNTHESIS OVER AN UNPROMOTED IRON CATALYST

被引:60
作者
AIKA, KI
OZAKI, A
机构
[1] Research Laboratory of Resources Utilization, Tokyo Institute of Technology, Meguro-ku, Tokyo, Ookayama
关键词
D O I
10.1016/0021-9517(69)90396-0
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 kinetics and deuterium isotope effect of the ammonia synthesis reaction over unpromoted iron catalyst have been studied at 305 °C. Some runs were carried out with mixtures of hydrogen and deuterium. The kinetic data as well as the isotope effect indicate that the rate-determining step is the chemisorption of nitrogen on a surface mainly covered with nitrogen atoms, and not with NH radicals as previously concluded for the doubly promoted catalyst. This result suggests that a part of the role of potash promoter is the change of the adsorbed species which retards the chemisorption process. © 1969.
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页码:232 / &
相关论文
共 9 条
[2]   ETHANE HYDROGENATION-CRACKING ON IRON CATALYSTS WITH AND WITHOUT ALKALI [J].
CIMINO, A ;
BOUDART, M ;
TAYLOR, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1954, 58 (09) :796-800
[3]  
KIRSHENBAUM I, 1951, PHYSICAL PROPERTIES
[4]  
KUBOTA H, 1959, CHEM ENG JAPAN, V23, P242
[5]   The catalytic decomposition of ammonia over iron synthetic ammonia catalysts [J].
Love, KS ;
Emmett, PH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1941, 63 :3297-3308
[6]  
MORIKAWA Y, IN PRESS
[7]   RATE EQUATION AND MECHANISM OF AMMONIA SYNTHESIS AT INDUSTRIAL CONDITIONS [J].
NIELSEN, A ;
KJAER, J ;
HANSEN, B .
JOURNAL OF CATALYSIS, 1964, 3 (01) :68-79
[8]   KINETICS AND MECHANISM OF THE AMMONIA SYNTHESIS [J].
OZAKI, A ;
TAYLOR, H ;
BOUDART, M .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1960, 258 (1292) :47-62
[9]  
Temkin M, 1940, ACTA PHYSICOCHIM URS, V12, P327