Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 10Citation - Scopus: 10Determination of the Particle Interactions, Rheology and the Surface Roughness Relationship for Dental Restorative Ceramics(Elsevier Ltd., 2009) Kes, Mürşide; Polat, Hürriyet; Keleşoğlu, Serkan; Polat, Mehmet; Aksoy, GökhanThe effect of inter-particle interactions on the slurry properties and the final surface roughness of the dental ceramic restoratives was investigated. A commercial dental ceramic powder, IPS Empress 2 veneer, was used as the raw material. The magnitudes of the particle-particle interactions were computed by the DLVO theory for the ceramic slurries of different electrolyte solutions (0.1 M, 0.25 M, 0.5 M, 0.75 M, 1 M NaCl and CaCl2). As expected, the energies of particle-particle interactions were influenced significantly by the presence of electrolytes. These computations demonstrated that addition of electrolytes leads to a progressive depression of the repulsive double layer forces. The absence of these forces should inevitably lead to agglomeration caused by the ever-present van der Waals forces. The rheological measurements carried out using the slurries with same solution properties supported the findings of the DLVO computations. It was found that dental ceramic slurries showed a Newtonian behavior in the absence of electrolytes, which is indicative of little or no agglomeration in the slurry. On the other hand, the same slurries displayed a non-Newtonian, shear thinning behavior in the presence of electrolytes which can be attributed to agglomeration or gelation. Roughness of the ceramic surfaces produced from these slurries was studied by SEM analysis and profilometer measurements. Contact angle studies were also carried out on the same surfaces. It was observed that the surface became rougher initially with electrolyte addition to a maximum, most probably due to formation of isolated agglomerates due to a reduction of the repulsive double layer forces. After reaching a maximum, surface roughness decreased to a much lower value with further increase in electrolyte concentration. This was most probably caused by the formation of a relatively homogeneous, gel-like structure within the extensively agglomerated slurry due to a complete collapse of the double layer.Conference Object Citation - WoS: 2Citation - Scopus: 2Investigation of the Permeability of Pure Gases in Sol-Gel Derived Al 2o 3 Membrane(Trans Tech Publications, 2004) Topuz, Berna; Çiftçioğlu, Muhsin; Özkan, FehimeThe preparation, characterization and pure gas permeation of sol-gel derived alumina membranes were investigated in this work. The effects of acid concentration/type and water content on the particle size in the sols and pore size distributions of the unsupported membrane were investigated by N 2 adsorption/desorption isotherms and Dynamic Light Scattering. Increasing the H +/Al 3+ mole ratio from 0.1 to 0.25 caused the hydrodynamic sol particle size and BJH pore size to decrease from 65 to 30 nm and 3.6 to 2.9 nm, respectively. The pore size increased from 2.8 nm to 3 nm upon increasing the calcination temperature from 500 to 600°C. Unsupported membranes were heat treated in the 200 to 1200 °C range for the characterization of the phase structure. Pinhole and crack free alumina membranes about 3 μm (2-layer) in thickness was observed from the SEM pictures with insignificant infiltration. The CO 2 permeability through the double layer γ-Al 2O 3 membrane calcined at 600 °C was 2.25*10 -7 mol/m 2.s.Pa, and had a slight pressure dependence indicating Knudsen Diffusion and Laminar Flow being the effective transport mechanisms. Upon the calcination of a similar 2-layer alumina membrane at 500°C, the CO 2 permeability decreased to 1.51 *10 -8 mol/m 2.s.Pa. without pressure dependence.Conference Object Citation - Scopus: 1Effects of Processing on the Properties and Permeability of Pure Gases Through Sol-Gel Silica Membranes(Trans Tech Publications, 2004) Topuz, Berna; Çiftçioğlu, Muhsin; Özkan, FehimeN2, O2 and CO2 pure gas permeation through sol-gel derived silica membranes were determined and the effects of processing parameters on the microstructure of the membrane was investigated. Silica sols were prepared in an alcoholic solution by hydrolysis and condensation of TEOS as a function of acid content. The thickness of the silica membranes was determined to be about 2μm and significant infiltration into the support was observed from the SEM pictures. The supported membranes were heat treated in the 50-400°C. The N2 permeabilities of silica membranes varied in the 2.2*10-10-2.7*10-8 mol/m2.s.Pa range for single layer membranes dipped for 10s. in the sol. The CO2 permeability of these membranes varied in the 1.2*10-9-6.95 *10-8 mol/m2.s.Pa range. The sols became viscous and gelled at 50°C in 16 hours. The O2 permeability increased with aging time. The optimum dipping time during processing was determined to be 10 seconds. The increase in the acid content of the sols were observed to increase permeabilities of the membranes significantly.