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On the Role of Zeolite Structure and Acidity in Toluene Acylation with Isobutyric Acid Derivatives

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    SYSNO ASEP0101103
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleOn the Role of Zeolite Structure and Acidity in Toluene Acylation with Isobutyric Acid Derivatives
    TitleVliv struktury různých typů zeolitů a jejich kyselosti na acylaci toluenu deriváty isobutyrové kyseliny
    Author(s) Klisáková, Jana (UFCH-W)
    Červený, L. (CZ)
    Čejka, Jiří (UFCH-W) RID, ORCID, SAI
    Source TitleApplied Catalysis A - General. - : ELSEVIER SCIENCE BV - ISSN 0926-860X
    Roč. 272, č. 1 (2004), s. 79-86
    Number of pages8 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordstoluene acylation ; isopropyltolyl ketone ; zeolite catalysts
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGA203/03/0804 GA ČR - Czech Science Foundation (CSF)
    KJB4040402 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    CEZAV0Z4040901 - UFCH-W
    AnnotationZeolite catalysts of various structures and type and concentration of acid sites were investigated in a liquid phase acylation of toluene with derivatives of isobutyric acid. The highest conversions of isobutyryl chloride or isobutyric anhydride were obtained over three-dimensional large pore zeolite Beta and zeolite Y possessing medium concentration of acid sites. In general, the conversion of acylating agents increases with increasing pore size diameter and dimensionality of the channel system. Large-pore zeolites with three-dimensional channel system enable easier desorption and transport of bulky isopropyltolyl ketone. The activity of the zeolites used can be also controlled by tailoring their hydrophobic/hydrophilic properties. The higher initial rate of toluene acylation with isobutyric anhydride compared to isobutyryl chloride was found. However, only one possible acylating group of isobutyric anhydride is used for acylation reaction.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2005
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