Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Preparation and Characterization of Hydroxyapatite Reinforced Polymeric Scaffolds(Natl Inst Science Communication-NISCAIR, 2025) Firata, Duygu Doga; Ersoz, Su Turku; Burcu Alp, Fatma; Cetin, Ali Emrah; Ciftcioglu, MuhsinPorous HA reinforced PLA/PCL scaffolds with polymer volume percentages in the 7.0-7.6 range have been prepared by solvent-casting/salt leaching technique. The scaffolds have been characterized by conducting gravimetric measurements, FTIR analysis, TGA, X-ray diffraction analysis, compression tests, cell viability tests, and thermal and hydrolytic degradation tests in order to investigate the effect of PLA/PCL, PLA/HA, PCL/HA and PLA/PCL/HA blending on scaffold properties. Porosity of the scaffolds has been determined to be in the 83-92 percent range. The scaffold porosity has decreased with HA content. The water absorption of the scaffolds has been found to be in between 400 and 750%. The yield strength and the elastic modulus of the scaffolds have been determined to be in the 0.001-0.02 and 5.6-10.6 MPa ranges, respectively. The yield strength of the scaffolds has increased by both PCL and HA contents whereas elastic modulus has increased with PCL content but has decreased with HA content. Mechanical test results have indicated that the addition of HA has increased the strength of the scaffolds while decreasing their flexibility. The activation energies for the thermal degradation of the scaffolds have been determined to be in the 130-398 kJ/mol range and have been shown to be a function of PCL, PLA, and HA content. The hydrolytic degradation behavior of the scaffolds in acetate buffer solutions (pH=4.5) during 127 days and XRD analysis have indicated that the hydrolytic degradation occurring in the amorphous part of the surface film has been diffusion-controlled. The diffusion coefficients of the degradation products in the scaffolds have been estimated to be in the 1.21-4.95x10(-13) m(2)/s range. Cell viability test results have indicated that the composition of the composite scaffold structure has played a determining role in the prepared scaffolds.Article A Room Temperature Chemical Process for Homogeneous Mixing of Precursor Phases for Low Temperature Tetracalcium Phoshate Preparation(Elsevier Sci Ltd, 2025) Cetin, Ali Emrah; Ciftcioglu, MuhsinThe aim of this study was to prepare phase pure tetracalcium phosphate (TTCP) from the precursor phase mixtures homogeneous at the nano/microscale level at lower heat treatment temperatures in much shorter dwell times. Two different precursor powder mixtures were prepared by reacting CaCO3 with H3PO4 in ethanol or water. The resultant precursor powder mixtures were heat treated at temperatures in the 1200-1350 degrees C range for 2 and 5 h. Phase structures of the powders were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) and Raman spectroscopy analysis. Scanning electron microscopy (SEM) was used for the investigation of powder particle sizes and morphology. Powders synthesized by the heat treatment of both of the starting powder mixtures prepared in ethanol or water with 2 and 5 h of dwell times at 1350 degrees C were determined to be phase pure TTCP. SEM analysis along with the phase identification showed that the precursor powder prepared in ethanol had micron sized plates formed by aggregation of sub-micron sized thin CaHPO4 plates covering CaCO3 particles. The precursor powder prepared in water contained large aggregates of sub-micron sized CaCO3 particles whose surface was covered by precipitated nano-sized hydroxyapatite. TTCP powders were composed of large irregularly shaped particles formed by sintering of smaller equiaxed grains. Average grain and particles sizes of the TTCP powders synthesized from the precursor powder prepared in ethanol were 3.2-3.9 and 8.1-8.4 mu m, respectively. Average grain and particle sizes of the TTCP powders synthesized from the precursor powder prepared in water however were measured to be 3.3-5.1 and 11.2-11.6 mu m, respectively. The TTCP preparation method presented in this study provides homogeneous and well-mixed precursor powders prepared from cheap and commonly available precursors without milling and decreases the heat treatment time to 2 h at 1350 degrees C.Article Citation - WoS: 6Citation - Scopus: 6Inverse Effects of Lanthanide Co-Doping on the Photocatalytic Hydrogen Production and Dye Degradation Activities of Cu Doped Sol-Gel Tio<sub>2</Sub>(Elsevier, 2023) Yurtsever, Husnu Arda; Erzin, Kubilay; Ciftcioglu, Muhsin; Yurtsever, Hüsnü Arda; Erzin, Kubilay; Çiftçioğlu, MuhsinCopper doped and lanthanide-copper co-doped titania powders were prepared by sol-gel technique and the effects of co-doping on the photocatalytic reduction and oxidation activities of titania were investigated in this work. Characterization studies indicated that a reduced structure was formed due to the presence of Ti3+ species in copper doped titania powder and a more stable structure was formed when lanthanides were used as co-dopants. Copper doped powder had a significantly higher activity in photocatalytic hydrogen production (1037 mu mol/g/h) than the co-doped powders (similar to 400 mu mol/g/h). The oxidation activities of co-doped powders however were determined to be about 2 times higher than that of the copper doped powder. The decrease in the reduction activity was attributed to the decrease in the number of Ti3+ sites, whereas the increase in oxidation activity was probably a result of the increase in the surface area and dye adsorption due to lanthanide co-doping.