DEACTIVATION OF STEAM-REFORMING MODEL CATALYSTS BY COKE FORMATION .2. PROMOTION WITH POTASSIUM AND EFFECT OF WATER

被引:49
作者
DEMICHELI, MC
DUPREZ, D
BARBIER, J
FERRETTI, OA
PONZI, EN
机构
[1] UNIV POITIERS, CATALYSE CHIM ORGAN LAB, CNRS, URA 350, F-86022 POITIERS, FRANCE
[2] CTR INVEST & DESARROLLO PROC CATALITICOS, LA PLATA, ARGENTINA
关键词
D O I
10.1006/jcat.1994.1054
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 influence of potassium on the hydrogenolysis of cyclopentane and on the simultaneous carbon formation over a series of alumina-supported Ni catalysts was studied. With increasing potassium loadings at temperatures where either a deactivating two. dimensional carbon or a filamentary carbon was formed, the catalytic activity passed through a maximum and then decreased. With relatively high K-doses there was less coking in the presence of steam; the growth of filamentary carbon was then largely reduced. Characterization of the coked catalysts by temperature-programmed oxidation and SEM disclosed quite different roles of alkali: at lower contents, associated with alumina, potassium facilitates the formation of filamentary carbon and minimizes the generation of coke precursors, whereas at higher contents it acts as a poison for both hydrogenolysis and coking reactions. In all cases, the alkali promoted the catalytic oxidation of the carbon deposits. Because of its localization, the alkali could also modify the nickel-carbon interface in carbon filaments. © 1994 Academic Press, Inc.
引用
收藏
页码:437 / 449
页数:13
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