Nature and Location of Carbonaceous Species in a Composite HZSM-5 Zeolite Catalyst during the Conversion of Dimethyl Ether into Light Olefins

被引:47
作者
Ibanez, Maria [1 ]
Perez-Uriarte, Paula [1 ]
Sanchez-Contador, Miguel [1 ]
Cordero-Lanzac, Tomas [1 ]
Aguayo, Andres T. [1 ]
Bilbao, Javier [1 ]
Castano, Pedro [1 ]
机构
[1] Univ Basque Country, UPV EHU, Dept Chem Engn, POB 644, Bilbao 48080, Spain
关键词
ZSM-5 (MFI) zeolite; dimethyl ether (DME); light olefins; propylene; coke; METHANOL CONVERSION; ENHANCED STABILITY; COKE FORMATION; HYDROCARBONS; TRANSFORMATION; DEACTIVATION; CRACKING; ACIDITY; H-ZSM-5; COKING;
D O I
10.3390/catal7090254
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
The deactivation of a composite catalyst based on HZSM-5 zeolite (agglomerated in a matrix using boehmite as a binder) has been studied during the transformation of dimethyl ether into light olefins. The location of the trapped/retained species (on the zeolite or on the matrix) has been analyzed by comparing the properties of the fresh and deactivated catalyst after runs at different temperatures, while the nature of those species has been studied using different spectroscopic and thermogravimetric techniques. The reaction occurs on the strongest acid sites of the zeolite micropores through olefins and alkyl-benzenes as intermediates. These species also condensate into bulkier structures (polyaromatics named as coke), particularly at higher temperatures and within the mesoand macropores of the matrix. The critical roles of the matrix and water in the reaction medium have been proved: both attenuating the effect of coke deposition.
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页数:13
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