Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 1From Chemistry to Clinic: Polysaccharide-Bioceramic Composites for Tissue Engineering Applications(Mary Ann Liebert, Inc, 2025) Yakubogullari, Nilgun; Yilmaz-Dagdeviren, Hilal Deniz; Arslan-Yildiz, AhuComposite scaffolds combining polysaccharides and bioceramics represent next-generation scaffolds extensively investigated in tissue engineering (TE) and biomedical applications. Polysaccharides such as chitosan, hyaluronic acid, and pectin mimic the extracellular matrix components with their tunable physicochemical properties, enabling a favorable microenvironment for cell adhesion, proliferation, and cell-matrix interactions. On the other hand, bioceramics, including calcium phosphate, hydroxyapatite, and bioactive glasses, enhance the mechanical properties of the material and offer structural integrity and osteoconductive properties. While they have generally been preferred to be used in bone TE and dental applications, various studies have also demonstrated their potential in cartilage regeneration, wound healing, and broader biomedical applications. Recent advancements in material design and scaffold fabrication techniques, particularly 3D printing and electrospinning, have provided precise engineering of materials and fabrication of scaffolds for desirable mechanical properties and biological performance. These innovations foster the development of patient-specific scaffolds, thereby paving the way for applications in personalized medicine. This review critically summarizes alternative polysaccharides, bioceramics, and composite materials used in TE and biomedical applications. It also highlights advanced fabrication strategies and finally explores the translational potential of these biocomposites. By integrating emerging technologies, this review aims to provide alternative and sustainable materials for the development of next-generation scaffolds that meet clinical needs.Impact Statement This study introduces polysaccharide-bioceramic composites with enhanced mechanical and biological properties for tissue engineering. Beyond bone and dental repair, their applications increasingly extend to wound healing, cartilage, cardiac, and muscle regeneration with drug delivery, angiogenesis, and neurogenesis. By mimicking the native extracellular matrix, these composites support cell growth and tissue regeneration, offering a versatile platform for advanced regenerative therapies.Article Citation - WoS: 9Citation - Scopus: 13Analysis of Adhesively Bonded Joints of Laser Surface Treated Composite Primary Components of Aircraft Structures(Elsevier, 2023) Martin, Seçkin; Nuhoğlu, Kaan; Aktaş, Engin; Tanoğlu, Metin; İplikçi, Hande; Barışık, Murat; Yeke, Melisa; Türkdoğan, Ceren; Esenoğlu, Gözde; Dehneliler, SerkanThe performance of the adhesively bonded aerospace structures highly depends on the adhesion strength between the adhesive and adherents, which is affected by, in particular, the condition of the bonding surface. Among the various surface treatment methods, as state of the art, laser surface treatment is a suitable option for the CFRP composite structures to enhance the adhesion performance, adjusting the roughness and surface free energy with relatively minimizing the damage to the fibers. The aim of this study is the validation and evaluation of the adhesive bonding behavior of the laser surface-treated CFRP composite structures, using the finite element technique to perform a conservative prediction of the failure load and damage growth. Such objectives were achieved by executing both experimental and numerical analyses of the secondary bonded CFRP parts using a structural adhesive. In this regard, to complement physical experiments by means of numerical simulation, macro-scale 3D FEA of adhesively bonded Single Lap Joint and Skin-Spar Joint specimens has been developed employing the Cohesive Zone Model (CZM) technique in order to simulate bonding behavior in composite structures especially skin-spar relation in the aircraft wing-box.Article Citation - WoS: 2Citation - Scopus: 10Water and Water Vapor Sorption Studies in Poly(propylene)-Zeolite Composites(John Wiley and Sons Inc., 2003) Pehlivan, Hilal; Özmıhçı, Filiz; Tıhmınlıoğlu, Funda; Balköse, Devrim; Ülkü, SemraWater and water vapor sorption to porous poly(propylene)zeolite composites prepared by hot pressing have been studied as a function of zeolite loading. This work presents the first report on the effect of the zeolite as a filler on the water sorption properties of PP composites. Water swelling experiments were conducted at 25°C using pure PP and PP-zeolite film samples having different zeolite loadings (6-40 wt%). Since PP is a hydrophobic polymer, it does not sorp any water, but the composites having 10, 20, 30, and 40% zeolite sorbed 0.63, 1.00, 1.72 and 3.74 wt% water, respectively. The zeolite itself at the same conditions sorbed 24.5 wt% water. As the filler loading in the composites increased, equilibrium uptake values increased too. On the other hand, water vapor sorption and kinetics has been studied using a Cahn 2000 gravimetric sorption system. Within in the range 0.35-0.95%, water vapor was adsorbed by the composites containing 10-40 wt% zeolite. Experimental effective water vapor diffusivities of the composite films were about one order of magnitude higher than the experimental water diffusion coefficient in composites. The transport of water in composites was slower than that in the liquid water due to the longer diffusion pathway and adsorption on the surface of the composites. Although the liquid water may fill all the voids in the composite, water vapor is adsorbed on the surface of the zeolite only.Article Citation - WoS: 19Citation - Scopus: 20Isothermal Crystallization Kinetics and Mechanical Properties of Polycaprolactone Composites With Zinc Oxide, Oleic Acid, and Glycerol Monooleate(John Wiley and Sons Inc., 2013) Alp, Burcu; Cesur, SerapThe isothermal crystallization and mechanical behavior of polycaprolactone (PCL) with zinc oxide (ZnO) with oleic acid and glycerol monooleate (GMO) were studied. Theoretical melting points calculated by the Flory-Huggins and Thompson-Gibbs models were thoroughly compared with differential scanning calorimetry experimental observations. The isothermal crystallization kinetic parameters by Avrami analysis showed that crystallization was controlled by nucleation, crystal growth was spherical, and the nucleation type changed between thermal and athermal nucleation. X-ray diffraction showed that when the additives were used together both the crystal thickness and the degree of crystallinity increased. A multiple-response regression analysis was made with the ZnO, oleic acid, and GMO concentrations as variables and the crystallinity as output. Interaction parameters by the Pukanzky model were calculated from the tensile strength at the yield point and indicated that the addition of oleic acid or GMO improved the interface between the ZnO particles and PCL.Article Citation - WoS: 17Citation - Scopus: 21Effects of Particle Size and Electrical Resistivity of Filler on Mechanical, Electrical, and Thermal Properties of Linear Low Density Polyethylene-Zinc Oxide Composites(John Wiley and Sons Inc., 2013) Özmıhçı Ömürlü, Filiz; Balköse, DevrimThe effects of particle size and electrical resistivity of zinc oxide (ZnO) on mechanical properties, electrical and thermal conductivities of composites made with linear low density polyethylene (LLDPE) were investigated. Micron sized (mZnO), submicron sized (sZnO), and nano sized (nZnO) powders having resistivities of 1.5 × 106, 1.5 × 109, and 1.7 × 108 were used to prepare composites with 5-20 vol % filler. The tensile strength was lowered and the modulus of elasticity of the composites was increased with ZnO addition. Rather than the particle size of the ZnO, its initial resistivity and aspect ratio affected the resistivity of composites. The resistivity of the LLDPE was lowered from 2.3 × 1016 Ω cm down to 1.4 × 1010 Ω cm with mZnO addition. Thermal conductivity of the composites was increased with ZnO addition 2.5-3 times of the polymer matrix. The composites can be used for electrostatically dissipating and heat sink applications due to their decreased electrical resistivity and increased thermal conductivity.Article Citation - WoS: 18Citation - Scopus: 19Effect of Zeolite Filler on the Thermal Degradation Kinetics of Polypropylene(John Wiley and Sons Inc., 2006) Pehlivan, Hilal; Balköse, Devrim; Ülkü, Semra; Tıhmınlıoğlu, FundaIn this study, the thermal degradation behavior of polypropylene (PP) and PP-zeolite composites was investigated, Clinoptilolite, a natural zeolitic tuff, was used as the filler material in composites. The effects of both pure clinoptilolite and silver-ion-exchanged clinoptilolite on the thermal degradation kinetics of the PP composites was studied with differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Polymer degradation was evaluated with DSC at heating rates of 5, 10, and 20°C/ min from room temperature to 500°C. The silver concentration (4.36, 27.85, and 183.8 mg of Ag/g of zeolite) was the selected parameter under consideration. From the DSC curves, we observed that the heat of degradation values of the composites containing 2-6% silver-exchanged zeolite (321-390 kj/kg) were larger than that of the pure PP (258 kj/kg). From the DSC results, we confirmed that the PPzeolite composites can be used at higher temperatures than the pure PP polymer because of its higher thermal stability, The thermal decomposition activation energies of the composites were calculated with both the Kissinger and Ozawa models. The values predicted from these two equations were in close agreement. From the TGA curves, we found that zeolite addition into the PP matrix slowed the decomposition reaction; however, silver-exchanged zeolite addition into the matrix accelerated the reaction. The higher the silver concentration was, the lower were the thermal decomposition activation energies we obtained. As a result, PP was much more susceptible to thermal decomposition in the presence of silver-exchanged zeolite.Article Citation - WoS: 48Citation - Scopus: 58Investigating the Effects of a Polyester Preforming Binder on the Mechanical and Ballistic Performance of E-Glass Fiber Reinforced Polyester Composites(Elsevier Ltd., 2003) Tanoğlu, Metin; Seyhan, Abdullah TuğrulAn experimental investigation was carried out to determine the effects of a preforming binder on the mechanical properties and ballistic performance of E-glass-fiber/polyester composite systems. The glass preforms were consolidated by application of heat and pressure over plies of the glass fabrics coated with various concentrations of a thermoplastic polyester binder. The peel strength of the preforms with various binder content was measured and the highest peel strength was obtained from preforms prepared with about 9 wt% of the binder. Composite laminates with and without binder were fabricated using VARTM technique and the effects of the binder on the composite mechanical properties were evaluated. It was found that the flexural strength and mode I interlaminar fracture toughness decreases by 15% and 40%, respectively, due to the presence of 3 wt% of the binder. Ballistic test was performed on E-glass/polyester composite panels using 1.1-g fragment-simulating projectiles and it was found that the binder amount has some considerable effect on the damage extension of the impacted composites. The results showed that the preforming binder has significant potential to tailor composite properties.Article Citation - WoS: 30Citation - Scopus: 31Water and Water Vapor Sorption Studies in Polypropylene-Zeolite Composites(Wiley, 2003) Pehlivan, Hilal; Özmıhçı, Filiz; Tıhmınlıoğlu, Funda; Balköse, Devrim; Ülkü, SemraWater and water vapor sorption to porous polypropylene-zeolite composites prepared by hot pressing have been studied as a function of zeolite loading. This work presents the first report on the effect of the zeolite as a filler on the water-sorption properties of PP composites. Water swelling experiments were conducted at 25°C using pure PP and PP-zeolite films samples having different zeolite loadings (6-40 wt %). Because PP is a hydrophobic polymer, it does not sorp any water, but the composites having 10, 20, 30, and 40% zeolites have sorbed 0.63, 1.00, 1.72 and 3.74% water, respectively. The zeolite itself at the same conditions sorbed 24.5% water. As the filler loading in the composites increased, equilibrium uptake values increased also. On the other hand, water vapor sorption and kinetics has been studied using a Cahn 2000 gravimetric sorption system. Within in the range of 0.35-0.95% water vapor was adsorbed by the composites containing 10-40 wt % zeolites. Experimental effective water vapor diffusivities of the composite films was about one order of magnitude higher (10-fold) than the experimental water diffusion coefficient in composites. The transport of water in composites was slower than that in the liquid water due to the longer diffusion pathway and adsorption on the surface of the composites. Although the liquid water may fill all the voids in the composite, water vapor is adsorbed on the surface of the zeolite only.
