Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 2Catalytic Activity of Heteropolytungstic Acid Encapsulated Into Mesoporous Material Structure(Walter de Gruyter GmbH, 2007) Gündüz, Gönül; Dimitrova, Rayna P.; Yılmaz, SelahattinThe 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: 23Citation - Scopus: 27Isomerization of Alpha-Pinene Over Acid Treated Natural Zeolite(Taylor and Francis Ltd., 2005) Ünveren, Ercan; Günüz, Gönül; Çakıcıoğlu Özkan, FehimeIn this study, isomerization of α-pinene was studied over several acid-treated natural zeolite catalysts rich in clinoptilolite. Zeolite samples were contacted with HCl at different concentrations at 30°'C or at 60°C for 3 and 24 hours and tested in isomerization reaction of alpha-pinene. The catalysts prepared were characterized by XRD, nitrogen adsorption, and acidity studies. Acidity strength and the distribution of Lewis and Brönsted acid sites of the catalysts were determined, and their catalytic activities in α-pinene isomerization and selectivities to main reaction products, camphene and limonene, were investigated. Acid treatment improved the selectivity of catalyst samples to camphene, decreasing the selectivity to limonene, probably forcing limonene to secondary reactions at high conversions. The kinetics of α-pinene consumption was described by first-order kinetics. Two kinetic models were tested for the reaction mechanism and one model was found to give a good correlation between the theoretical and experimental data. In the models, the key intermediate was the pinylcarbonium ion, which was formed irreversibly from α-pinene. Number and distribution of Lewis and Brönsted acid sites affect the formation of bicyclic and monocyclic products.