Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 50Citation - Scopus: 54Isomerization of ?-Pinene Over Calcined Natural Zeolites(Elsevier Ltd., 2004) Akpolat, Oğuz; Özkan, Seher Fehime; Özkan, Fehime; Beşün, Nurgün; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyIn this work, isomerization reaction of α-pinene was studied over several heat-treated natural zeolite catalysts, rich in clinoptilolite, from Balýkesir-Bigadic region in Turkey in a batch slurry reactor under nitrogen atmosphere. Zeolite samples were calcined at different temperatures such as 300, 450 and 600°C. All catalysts were tested in the isomerization reaction of α-pinene and were characterised by nitrogen adsorption experiments, IR, and XRD measurements. Acidity strength and the distribution of Lewis and Bronsted acid sites of the samples were determined. Selectivities to main reaction products, camphene and limonene, and reaction kinetics were investigated. Catalytic activity, that is total conversion of α-pinene, of heat-treated samples decreased with increasing calcination temperatures. Selectivity to limonene is dependent on α-pinene conversion at high conversion levels while the selectivity to camphene is not. The formation of heavy products increased with treatment temperature. It was seen that α-pinene consumption could be described by a first-order kinetics.Article Citation - WoS: 47Citation - Scopus: 52Isomerization of ?-Pinene Over Ion-Exchanged Natural Zeolites(Elsevier Ltd., 2003) Özkan, Fehime; Özkan, Seher Fehime; Akpolat, Oğuz; Beşün, Nurgün; Murzin, Dmitry Yu.; 03.02. Department of Chemical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyCatalysts prepared by ion exchange of clinoptilolite-based natural zeolite tuffs with NH4 +, Ba2+ and Pb2+ were investigated in the isomerization reaction of α-pinene at atmospheric pressure under nitrogen flow. Activity and selectivity to mono-, bi- and tricyclic products were correlated with acidity strength.