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Incorporation of Ti as a Pyramidal Framework Site in the Mono-Layered MCM-56 Zeolite and its Oxidation Activity

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    0517220 - ÚFCH JH 2020 RIV DE eng J - Journal Article
    Korzeniowska, A. - Grzybek, J. - Roth, W. J. - Kowalczyk, A. - Michorczyk, P. - Čejka, Jiří - Přech, J. - Gil, B.
    Incorporation of Ti as a Pyramidal Framework Site in the Mono-Layered MCM-56 Zeolite and its Oxidation Activity.
    ChemCatChem. Roč. 11, č. 1 (2019), s. 520-527. ISSN 1867-3880. E-ISSN 1867-3899
    R&D Projects: GA ČR GBP106/12/G015
    Institutional support: RVO:61388955
    Keywords : hydrothermal synthesis * selective-oxidation * hydrogen-peroxide * molecular-sieves * titanium * titanosilicate * mww * epoxidation * catalyst * silicalite * Zeolites
    OECD category: Physical chemistry
    Impact factor: 4.853, year: 2019
    Method of publishing: Limited access

    MWW zeolite MCM-56 with Al atoms on the surface was functionalized with Ti to produce pyramidal TiOH groups. This was carried out by removal of Al with nitric acid, calcination and treatment with titanium diisopropoxide bis(acetylacetonate) (Ti(acac)(2) (i-propoxide)(2), Ti(acac)(2)OiPr(2)). Up to 0.7% Ti was introduced. Using UV-Vis spectroscopy three types of Ti moieties were identified in the uncalcined materials tetrahedral in the framework, 5/6-coordinated Ti on the surface, presumably in the vacated pyramidal sites, and oxide-like clusters. The presence of TiOH on the surface was indicated by insitu measurement of UV-Vis spectra during calcination. It showed the band at 290nm, which disappeared at 500 degrees C, perhaps due to condensation with silanols. Catalytic oxidation tests were carried out with three samples containing 0.13, 0.36, and 0.70% Ti and methyl phenyl sulfide and cis-cyclooctene as model reactants. The study confirmed potential of the TiOH moieties in oxidation catalysis although their final form is not certain. Future studies will include increasing Ti content to enhance catalytic activity and better detection of this type of the Ti site.
    Permanent Link: http://hdl.handle.net/11104/0302500

     
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