Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 41Citation - Scopus: 43Isomerisation of ?-Pinene Over Beta Zeolites Synthesised by Different Methods(Elsevier Ltd., 2005) Gündüz, Gönül; Dimitrova, Raina D.; Yılmaz, Selahattin; Dimitrov, Ljubomir; Spassova, MayaLiquid-phase α-pinene isomerisation at l00°C in a batch reactor is studied over Beta zeolites synthesised by different methods. It is confirmed that α-pinene forms a carbenium ion in an acidic environment, which rearranges without capture by nucleophiles, to form mainly hydrocarbons as camphene, terpinenes, terpinolenes and heavy products. The microporous Beta samples show low activity despite the high acidity most probably because of the hindered intermediate formation. The nature of the enhanced activity of Beta mesopores samples is suggested to be a result from the high accessibility of the acidic sites. The isomerisation of α-pinene was studied over Beta zeolites synthesised by different methods. The main products are camphene, terpinenes, terpinolenes and heavy products. Beta zeolites with micro-/mesopores reveal excellent activity because of the appropriate balance between acidity and bimodal pore system. The microporous Beta samples show low activity despite the good total acidity most probably because of the steric effect for the formation of the intermediate cations.Article Citation - WoS: 32Citation - Scopus: 35Liquid Phase Transformation of ?-Pinene Over Beta Zeolites Containing Aluminium or Boron, Titanium and Vanadium as Lattice Ions(Elsevier Ltd., 2005) Gündüz, Gönül; Dimitrova, Raina D.; Yılmaz, Selahattin; Dimitrov, LjubomirBeta zeolites with different modules (SiO2/Al2 O3) and containing B, Ti or V in lattice positions were synthesised by different methods and tested as catalysts in liquid phase transformation of α-pinene at 100 °C in a batch reactor. It was established that the hydrogen forms of Beta samples with a SiO2/Al2O3 module of about 55-66 and containing both micro- and mesopores displayed high catalytic activity in liquid phase isomerization of α-pinene. Samples with boron, titanium or vanadium, as lattice ions possess insignificant catalytic activity.Article Citation - WoS: 50Citation - Scopus: 54Isomerization of ?-Pinene Over Calcined Natural Zeolites(Elsevier Ltd., 2004) Akpolat, Oğuz; Gündüz, Gönül; Özkan, Fehime; Beşün, NurgünIn 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; Gündüz, Gönül; Akpolat, Oğuz; Beşün, Nurgün; Murzin, Dmitry Yu.Catalysts 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.