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Selective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites

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    SYSNO ASEP0427874
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleSelective synthesis of linear alkylbenzene by alkylation of benzene with 1-dodecene over desilicated zeolites
    Author(s) Aslam, W. (SA)
    Siddiqui, M. A. B. (SA)
    Jermy, B. R. (SA)
    Aitani, A. (SA)
    Čejka, Jiří (UFCH-W) RID, ORCID, SAI
    Al-Khattaf, S. (SA)
    Source TitleCatalysis Today. - : Elsevier - ISSN 0920-5861
    Roč. 227, MAY 2014 (2014), s. 187-197
    Number of pages11 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordszeolites ; benzene alkylation ; long-chain olefin
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGBP106/12/G015 GA ČR - Czech Science Foundation (CSF)
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000332412900026
    EID SCOPUS84895479844
    DOI10.1016/j.cattod.2013.10.015
    AnnotationThe alkylation of benzene with 1-dodecene to linear alkylbenzenes (LAB) was investigated over 12-ring zeolites MOR, BEA, and FAU with varying framework topologies and Si/Alratios. The reaction was carried out under a high-pressure, 20 bar, in a fixed-bed flow reactor at 140 degrees C, using WHSV 4 h-1, benzene/1 dodecene molar ratio of 6.0 and time-on-stream of 6.0 h. In contrast to MOR and BEA zeolites, FAU exhibited the lowest selectivity (24%) to the desired 2-phenyl dodecane (2-LAB) due to its large cavities. The MOR and BEA with different Si/Alratios were further desilicated using alkali-metal treatments (0.2 M and 0.05 M NaOH) to create hierarchical porous structure. The desilication of both zeolites improved the conversion of 1-dodecene and the selectivity to 2-LAB. The excellent stability resulting from desilication is attributed to a better diffusivity of the LAB isomers, shortening of real contact time, due to the enhanced mesporous structure in both zeolites and the higher Lewis acidity. The selectivity to 2-LAB increased to 70% over desilicated MOR (Si/Al ratio = 20) compared with a selectivity of 35% over desilicated BEA (Si/Al ratio = 24).
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2015
Number of the records: 1  

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