On the location, strength and accessibility of Bronsted acid sites in hierarchical ZSM-5 particles

被引:60
作者
Tzoulaki, Despina [1 ,2 ]
Jentys, Andreas [1 ,2 ]
Perez-Ramirez, Javier [3 ]
Egeblad, Kresten [4 ]
Lercher, Johannes A. [1 ,2 ]
机构
[1] Tech Univ Munich, Dept Chem, D-85747 Garching, Germany
[2] Tech Univ Munich, Catalysis Res Ctr, D-85747 Garching, Germany
[3] ETH, Dept Chem & Appl Biosci, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[4] Tech Univ Denmark, Ctr Sustainable & Green Chem, DK-2800 Lyngby, Denmark
关键词
HZSM-5; Mesoporosity; Adsorption; Infrared spectroscopy; Bronsted acid sites; XYLENE ISOMERIZATION; ZEOLITES; MOLECULES; SORPTION; BENZENE; SURFACE; IR;
D O I
10.1016/j.cattod.2012.03.078
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Microporous and mesoporous (hierarchical) ZSM-5 samples, prepared by desilication, dealumination and templating with carbon nanoparticles have been characterized by adsorbing benzene, cyclohexane and 1,3,5-trimethylbenzene (mesitylene) to probe the location, the strength and the accessibility of Bronsted acid sites. The mesoporosity introduced by the methods explored resulted in a statistical accommodation of benzene at the channel intersections. Cyclohexane showed the highest strength of physisorption in micro-and mesopores and, thus, probes the largest fractions of acid sites. Mesitylene adsorption showed that mesopores of hierarchical zeolites do not contain Bronsted acid sites. All results indicated that the mesoporosity influences only the accessibility of the acid sites in the ZSM-5 crystals mostly via shortening diffusion pathways, but not the strength of the interaction with the cyclic hydrocarbons. The enhanced transport rates observed for benzene are associated to the decreased pore length inside the mesoporous particles, rather than to changes of the pore structure or the generation of additional sites. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:3 / 11
页数:9
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