Chemical Engineering / Kimya Mühendisliği

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

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Department: search.filters.department.İzmir Institute of Technology. Mechanical EngineeringWoS Q: search.filters.wosQuartile.Q2

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  • Article
    Citation - WoS: 29
    Citation - Scopus: 31
    Cure Kinetics of Epoxy Resin-Natural Zeolite Composites
    (Springer Verlag, 2008) Cansever Erdoğan, Beyhan; Seyhan, Abdullah Tuğrul; Ocak, Yılmaz; Tanoğlu, Metin; Balköse, Devrim; Ülkü, Semra
    The cure kinetics of epoxy resin and epoxy resin containing 10 mass% of natural zeolite were investigated using differential scanning calorimetry (DSC). The conformity of the cure kinetic data of epoxy and epoxy-zeolite system was checked with the auto-catalytic cure rate model. The results indicated that the hydroxyl group on the zeolite surface played a significant role in the autocatalytic reaction mechanism. This group was able to form a new transition state between anhydride hardener and epoxide group. The natural zeolite particles acted as catalyst for the epoxy system by promoting its curing rate.
  • Article
    Citation - WoS: 50
    Citation - Scopus: 54
    Isomerization of ?-Pinene Over Calcined Natural Zeolites
    (Elsevier Ltd., 2004) Akpolat, Oğuz; Gündüz, Gönül; Özkan, Fehime; Beşün, Nurgün
    In 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: 54
    Citation - Scopus: 62
    Sic-Particulate Aluminum Composite Foams Produced by Powder Compacts: Foaming and Compression Behavior
    (Springer Verlag, 2003) Elbir, Semih; Yılmaz, Selahattin; Toksoy, Ahmet Kaan; Güden, Mustafa; Hall, Ian W.
    The foaming behavior of SiC-particulate (8.6% by volume) aluminum composite powder compacts contained Titanium Hydride blowing agent was investigated by heating above the melting temperature (750°C) in a pre-heated furnace. Aluminum powder compacts were also prepared and foamed using similar compaction and foaming parameters in order to determine the effect of SiC-particulate addition on foaming and compression behavior. The linear expansions of the compacts at various furnace holding times were ex situ determined. Optical and scanning electron microscopy techniques were used to characterize prepared and deformed foams microstructures. The SiC-particulate addition was found to increase the linear expansion and reduce the extent of the liquid metal drainage and cell coarsening of the aluminum compacts. The composite foam samples also showed higher compressive stresses, but a more brittle behavior as compared with aluminum foams.