Influence of acidity on the H-Y zeolite performance in n-decane catalytic cracking: evidence of a series/parallel mechanism

被引:12
|
作者
Fonseca, N. [1 ,2 ]
Lemos, F. [1 ]
Laforge, S. [2 ]
Magnoux, P. [2 ]
Ribeiro, F. Ramoa [1 ]
机构
[1] Univ Tecn Lisbon, Inst Super Tecn, Ctr Biol & Chem Engn, IBB, P-1049001 Lisbon, Portugal
[2] Univ Poitiers, UMR 6503, Catalyse Chim Organ Lab, CNRS, F-86022 Poitiers, France
关键词
Catalytic cracking; n-decane; H-Y zeolites; Activity; Cracking mechanism; BRONSTED-TYPE EQUATIONS; METHYLCYCLOHEXANE TRANSFORMATION; ALKANES; OLEFINS; DEACTIVATION; TEMPERATURE; FEEDSTOCKS; STRENGTH; ZSM-5; WAXES;
D O I
10.1007/s11144-010-0197-8
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
In this work, n-decane cracking, taken as a model reaction for the catalytic cracking of Fischer-Tropsch naphta fraction, was carried out at 350 A degrees C over various H-Y zeolites, with different Si/Al ratios and, thus, different acid strength distributions. It was observed that the catalytic activity does not decrease gradually with the contact time for the catalysts under study, notably for the zeolite samples having lower activity (hence lower total acidity as well) but, in fact, the catalytic activity first increases with contact time and then decreases. This behavior was successfully interpreted by resorting to the fundamental view of the catalytic cracking mechanism as a series/parallel scheme. The authors combined the bi-molecular process involving a carbenium-chain mechanism and the protolytic process involving the formation of carbonium ions to construct a simple model to predict, in as much detail as possible, the zeolite catalytic performance of the different catalysts that were used.
引用
收藏
页码:249 / 263
页数:15
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