FAST CATALYTIC CRACKING OF HEAVY GAS OILS - MODELING COKE DEACTIVATION

被引:39
作者
LAROCCA, M
NG, S
DELASA, H
机构
[1] UNIV WESTERN ONTARIO,FAC ENGN SCI,CTR CHEM REACTOR ENGN,LONDON N6A 5B9,ONTARIO,CANADA
[2] DU PONT CANADA,DU PONT RES CTR,KINGSTON K7L 5A5,ONTARIO,CANADA
[3] CANADA CTR MINERAL & ENERGY TECHNOL,ENERGY RES LABS,OTTAWA K1A 0G1,ONTARIO,CANADA
关键词
D O I
10.1021/ie00098a005
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An unsteady-state pulse technique has been used to evaluate kinetic parameters for catalytic cracking of heavy gas oil with steamed commercial catalysts. The method closely mimic conditions of commercial FCC riser reactors. The experimental results obtained at a catalyst time-on-stream of under 20 s allowed the evaluation of activation energies and kinetic constants for gas oil decomposition into gasoline and light gas plus coke, as a whole, as well as for individual groups: paraffins, naphthenes, and aromatics. Two models were considered in the present study: (a) a three-lump model featuring gas oil, gasoline, and gas plus coke; (b) a five-lump model, where gas oil was split into paraffins, naphthenes, and aromatics. It was found that the catalyst deactivation due to coke formation, for contact times under 20 s, can be represented by both an exponential decay function and a power decay function with an average exponent of 0.1-0.2. © 1990, American Chemical Society. All rights reserved.
引用
收藏
页码:171 / 180
页数:10
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