Recent advances in reactions of alkylbenzenes over novel zeolites: The effects of zeolite structure and morphology

0506968 - ÚFCH JH 2020 RIV NL eng J - Článek v odborném periodiku
Al-Khattaf, S. - Ali, S. A. - Aitani, A. M. - Žilková, Naděžda - Kubička, D. - Čejka, Jiří
Recent advances in reactions of alkylbenzenes over novel zeolites: The effects of zeolite structure and morphology.
Catalysis Reviews-Science and Engineering. Roč. 56, č. 4 (2014), s. 333-402. ISSN 0161-4940. E-ISSN 1520-5703
Grant CEP: GA ČR GBP106/12/G015
Institucionální podpora: RVO:61388955
Klíčová slova: Alkyl aromatics * Dialkyl aromatics * Molecular sieves * Reaction kinetics * Zeolites
Obor OECD: Physical chemistry
Impakt faktor: 8.471, rok: 2014
Způsob publikování: Omezený přístup

Alkylbenzenes form an important segment of petrochemical industry for the manufacture of widely used commodities and specialty products. Since the last review on this topic (8), numerous new zeolite-based catalysts have been synthesized, characterized and evaluated in various transformations of aromatic hydrocarbons. This comprehensive review covers major reactions of mono-, di-, and tri-alkylbenzenes such as disproportionation, alkylation, transalkylation, isomerization, etc., over different zeolite-based acid catalysts. During the last decade, significant progress was made in the synthesis and structure determination of novel zeolites, mesoporous single crystals, hierarchic zeolites and two-dimensional zeolites. These developments have enhanced the understanding of the role of zeolites (effects of structural type, morphology, acid sites, accessibility of acid sites, shape selectivity factors) in transformations of aromatics. In this review, the emphasis is on the influence of the type of acid sites, zeolite topology, and reaction conditions on the activity, selectivity and pathways of these reactions. Thermodynamics and reaction kinetics of transformations of aromatic hydrocarbons are also discussed. This article covers mostly literature published during the period of 2002-2013.
Trvalý link: http://hdl.handle.net/11104/0298090