Optimizing the conversion of heavy reformate streams into xylenes with zeolite catalysts by using knowledge base high-throughput experimentation techniques

被引:81
作者
Serra, JM
Guillon, E
Corma, A
机构
[1] UPV CSIC, Inst Tecnol Quim, Valencia 46022, Spain
[2] CEDI Rene Navarre, Inst Francais Petrole, F-69390 Vernaison, France
关键词
xylenes; transalkylation; dealkylation; zeolites; heavy reformate; HTE;
D O I
10.1016/j.jcat.2005.03.021
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 [物理化学]; 081704 [应用化学];
摘要
The conversion of commercial heavy reformates under industrially relevant transalkylation conditions was studied over seven different acid zeolite catalysts with channel systems containing 10 MR, 12 MR, and 10 + 12 MR pores, by high-throughput experimentation (HTE). Zeolites were impregnated with seven different metals (Re, Pt, Mo, Ga, Ni, La, Bi). The reaction network for the global process was established, and the initial rates for primary reactions were estimated. It was found that zeolite pore size and geometry have a direct influence on dealkylation and transalkylation of the different alkyl groups. The ethyl and propyl dealkylation rate increases, while the rate of alkyl group transalkylation decreases as the zeolite pore dimensions decrease. A multizeolitic catalyst has been designed to optimize the dealkylation of ethyl and propyl aromatics while producing the transalkylation of tri- and tetramethylbenzene with toluene/benzene in order to maximize xylene yield when during the processing of heavy reformate. 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:342 / 354
页数:13
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