Mechanisms of coke growth on mordenite zeolite

被引：63

作者：

Chaouati, N. ^{[1
,2
]}

Soualah, A. ^{[2
]}

Chater, M. ^{[3
]}

Tarighi, M. ^{[1
]}

Pinard, L. ^{[1
]}

机构：

[1] Univ Poitiers, CNRS UMR7285, Inst Chim Milieux & Mat Poitiers, B27,TSA 51106,4 Rue Michel Brunet, F-86073 Poitiers 9, France

[2] Univ Bejaia, Fac Sci Exactes, Lab Physicochim Mat & Catalyse, Bejaia 06000, Algeria

[3] USTHB, Fac Chim, LEPCMAE, BP 32, El Alia 16111, Alger, Algeria

来源：

JOURNAL OF CATALYSIS | 2016年 / 344卷

关键词：

Coke; MALDI TOF; Mordenite; Deactivation; N-HEPTANE CRACKING; ETHANOL TRANSFORMATION; HZSM-5; ZEOLITE; DEACTIVATION; COKING; REGENERATION; PROPENE; ISOMERIZATION; DEPOSITS; USHY;

D O I：

10.1016/j.jcat.2016.10.011

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：

Mechanisms of coke formation and growth transformation on MOR zeolite were investigated using a microbalance at 623 K for two propene pressures: 0.1 and 1 bar. The low and high coking pressures correspond to laboratory and industrial conditions, respectively. Initial coke deposition is faster at high pressure, but the maximum uptake is higher at low pressure. The complete determination of chemical composition of coke has required the use of a lot of techniques (IRFT, GC-MS, MALDI-TOF). From the change of chemical composition of coke, it can be proposed by different mechanisms of growth of coke molecules trapped in the zeolite micropores. The coke grows under industrial conditions (high olefins pressure) by successive alkylation/cyclization/aromatization reactions, while under laboratory conditions (low olefins pressure) the growth proceeds preferentially by condensation of coke molecules. (C) 2016 Elsevier Inc. All rights reserved.

引用

页码：354 / 364

页数：11

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