Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 8Citation - Scopus: 9Polymeric Thermal Analysis of C+h and C+h+ar Ion Implanted Uhmwpe Samples(Elsevier Ltd., 2007) Kaya, N.; Öztarhan, Ahmet M.; Urkaç, Emel Sokullu; Ila, D.; Budak, S.; Oks, E.; Tıhmınlıoğlu, Funda; Muntele, C.Chemical surface characterization of C + H hybrid ion implanted UHMWPE samples were carried out using DSC (differential scanning calorimeter) and TGA (thermal gravimetric analysis) techniques. Samples were implanted with a fluence of 10(17) ion/cm(2) and an extraction voltage of 30 kV. The study of TGA and DSC curves showed that: (1) Polymeric decomposition temperature increased, (2) T-m, Delta C-p and Delta H-m values changed while Delta C-p and Delta H-m increased. T-g value could not be measured, because of some experimental limitations. However, the increase in Delta H-m values showed that T-g values increased, (3) the branch density which indicated the increase in number of cross-link (M-c) decreased in ion implanted samples and (4) increase in Delta H-m values indicated increase in crystallinity of implanted surface of UHMWPE samples.Article Citation - WoS: 25Citation - Scopus: 26Lowering the Sintering Temperature of Solid Oxide Fuel Cell Electrolytes by Infiltration(Elsevier Ltd., 2019) Sındıraç, Can; Çakırlar, Seda; Büyükaksoy, Aligül; Akkurt, SedatA dense electrolyte with a relative density of over 95% is vital to prevent gas leakage and thus the achievement of high open circuit voltage in solid oxide fuel cells (SOFCs). The densification process of ceria based electrolyte requires high temperatures heat treatment (i.e. 1400-1500 degrees C). Thus, the minimum co-sintering temperatures of the anode-electrode bilayers are fixed at these values, resulting in coarse anode microstructures and consequently poor performance. The main purpose of this study is to densify gadolinia doped ceria (GDC), a common SOFC electrolyte, at temperatures lower than 1400 degrees C. By this aim, an approach involving the infiltration of polymeric precursors into porous electrolyte scaffolds, a method commonly used for composite SOFC electrodes, is proposed. By infiltrating polymeric precursors of GDC into porous GDC scaffolds, a reduction in the sintering temperature by at least 200 degrees C is achieved with no additives that might affect the electrical properties. Energy dispersive x-ray spectroscopy line scan analyses performed on porous GDC scaffolds infiltrated by a marker solution (polymeric FeOx precursor in this case) reveals a homogeneous infiltrated phase distribution, demonstrating the effectiveness of polymeric precursors.Article Citation - WoS: 24Citation - Scopus: 26Self-Assembly Behavior of the Keratose Proteins Extracted From Oxidized Ovis Aries Wool Fibers(Elsevier Ltd., 2019) Pakkaner, Efecan; Yalçın, Damla; Uysal, Berk; Top, AybenWater soluble keratose proteins were obtained from an Ovis Aries wool using peracetic acid oxidation. The wool samples and the extracted keratose proteins were characterized by using FTIR, XRD, SEM and TGA techniques. Fractions of alpha-keratose (MW = 43-53 kDa) along with protein species with molecular weights between 23 kDa and 33 kDa were identified in the SDS-PAGE analysis result of the extracted protein mixture. DLS and AFM experiments indicated that self-assembled globular nanoparticles with diameters between 15 nm and 100 nm formed at 5 mg/ml keratose concentration. On the other hand, upon incubation of 10 w % keratose solutions at 37 degrees C and 50 degrees C, interconnected keratose hydrogels with respective storage modulus (G') values of 0.17 +/- 0.03 kPa and 3.7 +/- 0.5 kPa were obtained. It was shown that the keratose hydrogel prepared at 37 degrees C supported L929 mouse fibroblast cell proliferation which suggested that these keratose hydrogels could be promising candidates in soft tissue engineering applications. (C) 2018 Elsevier B.V. All rights reserved.Article Citation - WoS: 23Citation - Scopus: 24Investigation of Kinetics of Supercritical Drying of Alginate Alcogel Particles(Elsevier Ltd., 2019) Şahin, İbrahim; Uzunlar, Erdal; Erkey, CanSpherical calcium alginate gel particles were synthesized by dripping method. The effects of temperature, pressure, particle size and CO2 flow rate on kinetics of supercritical drying of alginate gel particles in a packed bed were investigated. Increase in CO2 flow rate, increase in temperature and decrease in particle size increased the drying rate and decreased the drying time. A mathematical model based on (i) the diffusion of the solvent inside the pores of gel particles, (ii) external mass transfer of the solvent from the surface of the gel particles into the flowing fluid stream, and (iii) convection and axial dispersion of the solvent in the flowing fluid stream was developed. A correlation for predicting external mass transfer coefficients for supercritical drying of alcogel particles was developed by fitting the model to experimental data. A good agreement between the experimental data and model results was achieved using the developed correlation.Article Citation - WoS: 27Citation - Scopus: 31Fluoroacrylate-Aromatic Acrylate Copolymers for Viscosity Enhancement of Carbon Dioxide(Elsevier Ltd., 2019) Kılıç, Sevgi; Enick, Robert M.; Beckman, Eric J.The effect of the structure of aromatic acrylate-fluoroacrylate copolymers on CO2 viscosity at elevated pressures was investigated. These copolymers were all found to be miscible with CO2 at pressures between 10-15 MPa (295 K) and induce an increase in the viscosity to some degree. It appears that stacking of aromatic rings is the key factor in viscosity enhancement. The results showed that viscosity of the solution increases with the increasing content of the aromatic acrylate unit in the copolymer, but a point is reached beyond which additional comonomer causes the relative viscosity to drop, suggesting that the aromatic rings associate through intramolecular rather than intermolecular interactions beyond the optimum value. The most effective CO2 thickener identified in this study was the 29% phenyl acrylate-71% fluoroacrylate copolymer. However, the presence of a spacer (methyl or ethyl) between the backbone and the aromatic group substantially diminished the viscosity enhancement.Article Citation - WoS: 15Citation - Scopus: 19Brominated Flame Retardants in a Computer Technical Service: Indoor Air Gas Phase, Submicron (pm1) and Coarse (pm10) Particles, Associated Inhalation Exposure, and Settled Dust(Elsevier Ltd., 2019) Genişoğlu, Mesut; Sofuoğlu, Aysun; Kurt Karakuş, Perihan Binnur; Birgül, Aşkın; Sofuoğlu, Sait CemilBrominated flame retardants (BFRs) are found in multi-media indoors, therefore, may pose serious risks to human health. This study investigated the occurrence of BFRs in particulate matter (PM1 and PM10) and gas phase by active and passive sampling, and settled dust to estimate potential exposure in a computer technical service. Polybrominated diphenyl ethers (PBDEs) and their alternatives (novel BFRs, NBFRs) were studied. PM and gas phase were collected on glass fiber filters and polyurethane foam plugs, respectively, and analyzed with a GC/MS after extraction, clean-up, and concentration. Inhalation exposure of the staff was estimated based on the measured concentrations using Monte Carlo simulation. BDE-209 was the dominating PBDE congener in all media while bis(2-ethylhexyl)-3,4,5,6-tetrabromophthalate and 1,2-bis(2,4,6-tribromophenoxy)ethane were those of NBFRs. Submicron particulate matter (PM1) BFR levels constituted about one half of the PM10-associated concentrations, while average PM10 mass concentration (69.9 μg m−3) was nine times that of PM1 (7.73 μg m−3). Calculated log10 dust-gas and PM-gas partitioning coefficients ranged from −5.03 to −2.10, −2.21 to −0.55, and −2.26 to −1.04 for settled dust, PM10, and PM1, respectively. The indoor/outdoor concentration ratios were >1 for all compounds indicating the strength of indoor sources in the service. The estimated potential inhalation exposures, for future chronic-toxic and carcinogenic risk assessments, indicated that the levels of gas-phase and PM1-associated exposures were similar at approximately one half of PM10-associated levels. Results of this study indicate that the occurrence of BFRs in all studied media should be taken into consideration for occupational health mitigation efforts.Article Citation - WoS: 34Citation - Scopus: 35Development of High Flux Nanofiltration Membranes Through Single Bilayer Polyethyleneimine/Alginate Deposition(Elsevier Ltd., 2019) Tekinalp, Önder; Alsoy Altınkaya, SacideThe aim of this study is to prepare high flux, stable, antifouling nanofiltration membranes through single bilayer polyelectrolyte deposition. To this end, a tight ultrafiltration support membrane was prepared from a polysulfone/sulfonated polyethersulfone blend. Deposition of a polyethyleneimine and alginate pair on this support has reduced the molecular weight cut off from 6 kDa to below 1 kDa. The pure water permeability and polyethylene glycol 1000 rejection of the coated membrane were found to be 15.5 ± 0.3 L/m2·h·bar and 90 ± 0.6%, respectively, by setting the deposition pH for each layer to 8 and the ionic strengths to 0.5 M and 0 M. This membrane has exhibited significantly higher permeability than commercial membranes with the same molecular weight cut off, retaining 98% of the initial flux during 15 h filtration of bovine serum albumine. In addition, the membrane has been able to completely remove anionic dyes from aqueous solution by showing 99.9% retentions to Reactive red 141, Brilliant blue G and Congo red with a 2 bar transmembrane pressure. High flux and membrane stability in acidic and salty environments have been achieved when deposition conditions favor high adsorption levels for the first layer and strong ionic cross-linking between the carboxyl group on the alginate and the amine groups on the polyethyleneimineArticle Citation - WoS: 49Citation - Scopus: 55A Facile Approach for Preparation of Positively Charged Nanofiltration Membranes by In-Situ Crosslinking Between Polyamide-Imide and Polyethylenimine(Elsevier Ltd., 2018) Cihanoğlu, Aydın; Alsoy Altınkaya, SacidePolyamide-imides (PAI) are attractive materials for membrane formation due to their high chemical and thermal stability. In this study, we report a facile approach for preparing positively charged nanofiltration (NF) membranes using a one-step process. Polyethylenimine (PEI) was dissolved in a coagulation bath and formed in-situ ionic crosslinking with PAI during phase inversion. The membranes were characterized by attenuated total reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), atomic force microscopy (AFM), contact angle and zeta potential measurements. The most positively charged membrane was obtained when the pH of the coagulation bath was adjusted to 10. This membrane showed a significant decrease in contact angle and surface roughness and increase in the pure water permeability (PWP) compared to the plain PAI membrane. The salt rejection performance of the crosslinked PAI membrane was measured using MgCl2, CaCl2, NaCl and Na2SO4 salts. The rejection of Mg2+ and Ca2+ ions was found to be 95.6% and 90.2%, respectively. The crosslinked membrane showed excellent chemical stability when stored in HCl solution at pH 3 up to 7 days. Antifouling behaviour of the optimized membrane was tested using bovine serum albumin (BSA) and flux recovery ratio of the membrane was found to be 92.2% at the end of 3 h filtration. The results suggest that the positively charged PAI membranes crosslinked with PEI may have a potential in recovering valuable cationic metals from acid mine wastewater.Article Citation - WoS: 15Citation - Scopus: 13Phase Behavior of Dspc/Peg40st Mixtures at Higher Emulsifier Contents(Elsevier Ltd., 2018) Kılıç, Sevgi; Bölükçü, Elif ŞenizPhase behaviors of 1,2-Distearoyl-sn-glycero-3-phosphocholine (DSPC) and polyoxyethylene(40)stearate (PEG40St) were investigated with Langmuir monolayer isotherms and Brewster angle microscopy (BAM) imaging at DSPC/PEG40St molar ratios ranging from 9:1 to 5:5. Two plateaus were found in the Langmuir isotherms which were relatively shorter for the 9:1 mixture and extended significantly by increasing the PEG40St content, indicating that the PEG40St squeezed out whereas more emulsifier retained in the monolayer at higher PEG40St contents. A strong hysteresis was observed when the mixed monolayers were subjected to compression-expansion cycles. The degree of hysteresis for the first cycles also increased with increasing PEG40St content in the monolayer. Gray scale intensities in the Brewster angle microscopy images were determined for pure DSPC and pure PEG40St and a scale was established to better interpret the morphologies for the mixtures. Bud and vessels formed during the PEG40St squeezed out upon compression. Upon expansion, PEG40St and DSPC is reappeared on the monolayer. When considered BAM images together with the Langmuir isotherm, PEG40St molecules were found to be well distributed within the DSPC molecules at lower DSPC/PEG40St mole ratios and mostly phase separated at higher mole ratios. It was concluded that higher PEG40St content would be advantageous for the design of an efficient and cheaper ultrasound contrast agents.Article Citation - WoS: 51Citation - Scopus: 60Biosilica Incorporated 3d Porous Scaffolds for Bone Tissue Engineering Applications(Elsevier Ltd., 2018) Tamburacı, Sedef; Tıhmınlıoğlu, FundaAs a natural and abundant silica mineral, diatomite particles (SiO2-nH2O) have been used in several areas such as filtration, photonics, sound and heat insulation, filler material and drug delivery due to its abundance, inexpensive cost, unique morphology and porous structure. But up to date, diatomite incorporated silica based scaffolds have not been used for bone tissue engineering applications. In the present study, the goal was to combine the useful biomaterial properties of both chitosan and diatomite as biocomposite organic/inorganic biomaterial for bone tissue engineering applications and optimize the silica content of the composites in order to obtain optimum morphological structure, high mechanical properties, enlarged surface area and enhanced cell proliferation. The effect of silica loading on the mechanical, morphological, chemical, and surface properties, wettability and biocompatibility of composite scaffolds were investigated. In addition, in vitro cytotoxicity and cellular activities including cell proliferation, ALP activity and biomineralization were investigated in order to determine biological activity of the composite scaffolds. Diatomite particles lead to enhancement in the water uptake capacity of scaffolds. Chitosan-silica composites exhibited 82–90% porosity. Wet chitosan-silica composite scaffolds exhibited higher compression moduli when compared to pure chitosan scaffold in the range of 67.3–90.1 kPa. Average pore size range of chitosan-diatomite composite scaffolds was obtained as 218-319 μm. In vitro results indicated that chitosan-diatomite composites did not show any cytotoxic effect on 3T3, MG-63 and Saos-2 cell lines. Scaffolds were found to be favorable for osteoblast proliferation. Diatomite incorporation showed promising effects on enhancing ALP activity as well as mineral formation on scaffold surface. Thus, the prepared scaffolds in this study can be considered prospective material for bone tissue engineering applications.