Deactivation kinetics of Ag/Al2O3 catalyst for ethylene epoxidation

被引:21
|
作者
Boskovic, G [1 ]
Dropka, N [1 ]
Wolf, D [1 ]
Brückner, A [1 ]
Baerns, M [1 ]
机构
[1] Inst Appl Chem Berlin Adlershof, D-12489 Berlin, Germany
关键词
deactivation; kinetics; ethylene epoxidation; accelerated deactivation; deactivation compensation;
D O I
10.1016/j.jcat.2004.06.003
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
Deactivation kinetics of a commercial Ag/Al2O3 catalyst was investigated using accelerated deactivation tests in a Berty-type gradientless recycle reactor. Separability of catalytic reaction and deactivation kinetics were established by operation in a "deactivation compensation" mode, keeping temperature and oxygen concentration constant. It was shown that sintering is the main source for deactivation and that kinetics of deactivation can be described by using a general power-law equation with an order of deactivation equal to 1 with respect to the driving force (a - a(ss)), a being the time-dependent activity and a(ss) the final steady-state activity after an extended period of catalyst operation. The long-time prediction of catalyst behavior suggested that an improved catalyst should work at a lower temperature to avoid sintering. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:334 / 342
页数:9
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