Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

Browse

Search Results

Now showing 1 - 2 of 2
  • Article
    Citation - WoS: 2
    Catalytic Activity of Heteropolytungstic Acid Encapsulated Into Mesoporous Material Structure
    (Walter de Gruyter GmbH, 2007) Gündüz, Gönül; Dimitrova, Rayna P.; Yılmaz, Selahattin
    The paper presents a spectroscopic and catalytic study of encapsulated Keggin type heteropoly acid (12-tungstophosphoric acid, HPW) in the mesopores of MCM-41 molecular sieves. Nitrogen physisorption, FTIR, SEM, XRD and catalytic methods have been used to characterize and compare the properties of the samples. Methanol conversion, alpha-pinene isomerization and ethyl acetate oxidation have been applied as model reactions for the evaluation of acid site activity. The combined physicochemical and catalytic investigations clearly show that the introduction of 12-tungstophosphoric acid into MCM-41 causes significant changes in the properties of the sample.
  • Article
    Citation - WoS: 11
    Citation - Scopus: 11
    Effect of Different Acidity Modifications on the Activity and Selectivity on H-Zsm5 Zeolites in N-Butene Isomerization
    (Springer Verlag, 2014) Kılıç, Emre; Yılmaz, Selahattin
    H-ZSM-5 was modified by silylation [tetraethylorthosilicate (TEOS) and triaminopropyltriethoxysilane], alkali (NaOH), acid (HCl) and ammoniumhexafluorosilicate (AHFS) treatments. The parent and modified zeolite forms were tested in n-butene isomerization. Modifications affected total acidities, the strength of the acid sites, pore sizes and surface areas of the H-ZSM-5 differently. The modifications decreased the conversion obtained by the parent catalyst. TEOS and alkali modifications did not promote formation of isobutene. Pre-alkali treatment before acid treatment increased selectivity to isobutene from 56.0 to 66.7 %, while conversion changed a little, it dropped from 52 to 50 %. AHFS modification provided the highest enhancement in selectivity to isobutene (87.5 %) for which n-butene conversion was dropped by about 10 % compared to H-ZSM-5. This was attributed to a slight modification of the pore size and to the reduction in strong and weak acid sites and generation of new Lewis acid sites.