Person: KAHRAMAN, MEMET VEZİR
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KAHRAMAN
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MEMET VEZİR
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Publication Metadata only alpha-Amylase immobilization on functionalized nano CaCO3 by covalent attachment(WILEY-V C H VERLAG GMBH, 2012) KAHRAMAN, MEMET VEZİR; Demir, Serap; Gok, Sevda Burcu; Kahraman, Memet VezirIn this study, a-amylase was immobilized on glutaraldehyde activated silanized calcium carbonate nanoparticles by a using covalent binding method. The surface modified nano calcium carbonate (CaCO3) were characterized using FTIR and SEM. Immobilization yield was found as 199.43 mg/g of calcium carbonate nanoparticles. The maximum activity was observed at pH 6.5. The immobilized enzyme had a higher activity at elevated temperature (5090 degrees C) than the free one. Reuse studies demonstrated that the immobilized enzyme could reuse 25 times while retaining 18.2% of its activity. Free enzyme lost its activity completely within 15 days. Vmax values for the free and immobilized enzymes were calculated as 10 and 0.35 mg/mL/min, respectively.Publication Metadata only Nanodiamond-containing polyethyleneimine hybrid materials for lead adsorption from aqueous media(WILEY, 2019) KAHRAMAN, MEMET VEZİR; Cigil, Asli Beyler; Urucu, Oya Aydin; Kahraman, Memet VezirThis study describes the preparation of new surface-modified nanodiamond (ND) particles containing urethane-based hybrid materials by photopolymerization of aliphatic urethane acrylate, trimethylolpropane triacrylate, glycidyl methacrylate monomers, and their usage for lead adsorption from aqueous media. ND and synthesized surface-modified ND were characterized by atom transfer radical addition Fourier transform infrared spectroscopy (ATR-FTIR) and scanning transmission electron microscopy analysis. Crosslinked adsorbent nanocomposites were then treated with polyethylene imine and all adsorbent nanocomposites were characterized by ATR-FTIR, scanning electron microscopy, thermogravimetric analysis, and contact angle measurements. The metal ion binding capacity of the surfaces of the nanocomposites containing high amine content was investigated. The effects of the percentage of functional monomer, pH, and contact time on adsorption, and the interaction of foreign metal ions have been tested. Optimum contact time was found to be 7 h at pH 5. The adsorption capacity of the synthesized nanocomposite adsorbent for lead (II) was determined as 17.12 mg g(-1). Langmuir and Freundlich isotherms were used to determine the adsorption behaviors and Langmuir isotherm model was found to be the most suitable model (R-2: 0.9988). The amount of adsorption of Pb (II) ions of UV curable adsorbent film prepared in river water samples was investigated. (c) 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 48241.Publication Metadata only Thermal, optical and electrical properties of UV-curing screen-printed glass substrates(SPRINGER, 2019) ARMAN KANDIRMAZ, EMİNE; Cigil, Asli Beyler; Kandirmaz, Emine Arman; Birtane, Hatice; Kahraman, Memet VezirIn this study, the hydroxyl functionality of the polyaniline surface was obtained using hydroxyethyl methacrylate and acrylated with isocyanatoethyl methacrylate. Coating formulation being curable with UV was designed by mixture of acrylated PANI (a-PANI) (0-5wt%), polyethylene glycol diacrylate, trimethylolpropane triacrylate, hydrolyzed 3-(methacryloxy) propyl trimethoxysilane (hydMEMO) and photoinitiator. The hybrid composite formulation has been printed on the glass surface with the method of screen printing. The chemical structure and the properties of thermal, electrical and surface obtained products were determined with ATR-FTIR, goniometer, current-voltage meter, scanning electron microscopy (SEM) and thermogravimetric analysis. ATR-FTIR results have shown that all materials were clearly produced. SEM results have revealed that PANI was dispersed at the composite in a stable manner. The conductivity value of the conductive line printed with F5a-PANI was found to be 3.7x10(-3)S. The best electrical results have presented that PANI has been beneficial for conductive line, and thus, screen printing was a convenient method for printing conductive lines.Publication Metadata only Preparation and Characterization of Thermally Conductive Thermoplastic Polyurethane/h-BN Nanocomposites(WILEY, 2014) ÇAKMAKÇI, EMRAH; Cakmakci, Emrah; Kocyigit, Ciler; Cakir, Selma; Durmus, Ali; Kahraman, M. VezirPublication Metadata only Alpha-Amylase Immobilization on Epoxy Containing Thiol-Ene Photocurable Materials(KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY, 2013) ÇAKMAKÇI, EMRAH; Cakmakci, Emrah; Danis, Ozkan; Demir, Serap; Mulazim, Yusuf; Kahraman, Memet VezirThiol-ene polymerization is a versatile tool for several applications. Here we report the preparation of epoxide groups containing thiol-ene photocurable polymeric support and the covalent immobilization of alpha-amylase onto these polymeric materials. The morphology of the polymeric support was characterized by scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) coupled with SEM was used to explore the chemical composition. The polymeric support and the immobilization of the enzyme were characterized by FTIR analysis. SEM-EDS and FTIR results showed that the enzyme was successfully covalently attached to the polymeric support. The immobilization efficiency and enzyme activity of alpha-amylase were examined at various pH (5.0-8.0) and temperature (30-80 degrees C) values. The storage stability and reusability of immobilized alpha-amylase were investigated. The immobilization yield was 276 +/- 1.6 mg per gram of polymeric support. Enzyme assays demonstrated that the immobilized enzyme exhibited better thermostability than the free one. The storage stability and reusability were improved by the immobilization on this enzyme support. Free enzyme lost its activity completely within 15 days. On the other hand, the immobilized enzyme retained 86.7% of its activity after 30 days. These results confirm that alpha-amylase was successfully immobilized and gained a more stable character compared with the free one.Publication Metadata only Immobilization of alpha- amylase on aminated polyimide membrane: Preparation, characterization, and properties(WILEY-V C H VERLAG GMBH, 2014) ÇAKMAKÇI, EMRAH; Cakmakci, Emrah; Cigil, Asli Beyler; Danis, Ozkan; Demir, Serap; Kahraman, Memet Vezir-amylase was covalently immobilized on functionalized polyimide (PI) membranes via glutaraldehyde (GA) activation. 3,3,4,4-Benzophenonetetracarboxylic acid dianhydride (BTDA) and 4,4-oxydianline (4,4-ODA) based polyimide membranes were obtained via thermal imidization. Free amine groups on the surface of the polyimide membranes were generated by the amination reaction of polyimides with hexamethylenediamine (HMDA). Surface-aminated membranes were subjected to enzyme immobilization after GA activation. Immobilization efficiency and enzyme activity of -amylase was examined at various pH (3.0-8.0) and temperature (15-80 degrees C). The storage stability and reusability of immobilized -amylase were investigated. Immobilization yield was found as 359.53mg per gram of modified polyimide films. Enzyme assays demonstrated that the immobilized enzyme exhibited better thermo stability than the free one. The storage stability and reusability improved by the immobilization on this enzyme support. Free enzyme lost its activity completely within 15 days. On the other hand, the immobilized enzyme retained 79.98% of its activity after 30 days. These results confirmed that -amylase was successfully immobilized and gained more stable character compared to the free enzyme.Publication Metadata only Polymeric nanoparticles for selective protein recognition by using thiol-ene miniemulsion photopolymerization(TAYLOR & FRANCIS LTD, 2020) KAHRAMAN, MEMET VEZİR; Yasar, Merve; Dal Yontem, Fulya; Kahraman, M. Vezir; Apohan, Nilhan Kayaman; Aktas, Zerrin; Oncul, Mustafa Oral; Akcakaya, HandanThe fabrication of molecularly imprinted nanoparticles (MIP-NPs) specific for myoglobin by using thiol-ene photopolymerization in miniemulsion was described. Allyl derivatives of phenylalanine as a functional monomer was synthesized and copolymerized with acrylic monomersviaminiemulsion polymerization to produce NIP-NPs with approximately 74 nm number average particle diameter. FTIR and(1)H-NMR analysis confirmed the synthesis of functional monomer. MIP-NPs were prepared in the existence of myoglobin as a template protein. Morphological investigations exhibited that the particle size of the MIP-NPs, increased compared to the corresponding NIPs and the mean particle diameter by number was measured as 141 nm with narrow distribution. NIP-NPs that were polymerized without myoglobin were found to have less affinity to the target protein. In addition, the rebinding ability of MIP-NPs was much bigger than that of the corresponding NIPs. ELISA results showed that MIPs interact particularly with the myoglobin and show little affinity for BSA in competitive binding experiments.Publication Metadata only Thermal and Phase Change Material Properties of Comb-Like Polyacrylic Acid-Grafted-Fatty Alcohols(TAYLOR & FRANCIS INC, 2018) KAHRAMAN, MEMET VEZİR; Basturk, Emre; Kahraman, Memet VezirPoly(acrylic acid)-graft-fatty alcohol are synthesized from the esterification of polyacrylic acid with octadecanol and docosanol. The characterization of poly(acrylic acid)-graft-fatty alcohol was performed by attenuated total reflection-Fourier transform infrared spectroscopy. The thermal stability performances and phase change behaviors of poly(acrylic acid)-graft-fatty alcohol were examined by using thermogravimetric analysis system and differential scanning calorimetry. The results indicate that the poly(acrylic acid)-graft-fatty alcohol polymeric phase change materials possess good phase change properties and provide a suitable working temperature range. The heating process phase change enthalpy is measured between 112 and 122J g(-1), and the freezing process phase change enthalpy is found between 118 and 126J g(-1). The decomposition of poly(acrylic acid)-graft-fatty alcohol polymeric phase change materials started at 177 degrees C and reached a maximum of 380 degrees C. All of the obtained poly(acrylic acid)-graft-fatty alcohol polymeric phase change materials improved latent heat storage capacity in comparison with the pristine poly(acrylic acid) polymer. With the obtained results we conclude that, these materials promise a great potential in thermal energy storage applications. [GRAPHICS]Publication Metadata only Dual microcapsules based epoxy/polyethyleneimine autonomous self-healing system for photo-curable coating(WILEY, 2021) KAHRAMAN, MEMET VEZİR; Tezel, Ozge; Beyler Cigil, Asli; Kahraman, Memet VezirSelf-healing coatings were fabricated by adding two different epoxy and polyethyleneimine microcapsules to epoxy-polyester acrylate resin. The first capsule contained polyethyleneimine and the second capsule contained a commercial epoxy resin. Polyethyleneimine (PEI) microcapsules were prepared by filling PEI into hollow poly(melamine-urea-formaldehyde) (PMUF)-shelled polymeric microcapsules. Epoxy microcapsules were prepared by coating with a poly(urea-formaldehyde) (PUF)-shelled material using in-situ polymerization. Using thermogravimetric analysis (TGA), the healing agent contents of the microcapsules for epoxy and PEI were determined to be 55% and 49%, respectively. Moreover, using a zeta-sizer, the mean sizes of the microcapsules for epoxy/PUF and PEI/PMUF were determined to be 185 nm and 377 nm, respectively. Both capsule types were added to the epoxy-polyester acrylate-based photo-curable coating formulation in the amount of 2% by weight. The coating formulation was applied to plexiglass surface, then cured with UV light and artificial scratches were made on the coating surface. At the end of day two, the SEM images revealed that coating successfully self-healed the scratch.Publication Metadata only Design and development of self-healing coating based on thiol-epoxy reactions(ELSEVIER, 2019) KAHRAMAN, MEMET VEZİR; Tezel, Ozge; Cigil, Asli Beyler; Kahraman, Memet VezirCracks caused by the effects of mechanical or chemicals forces on coatings may cause their performance to deteriorate and may shorten their lifetime. The microcapsules used for self-healing coatings provide automatic recovery and extend the life of the coatings. In this study, polyurea-formaldehyde epoxy resin (PUF-epoxy) microcapsules were synthesized by in-situ polymerization; because, they allow the size control of the microcapsules, the thickness of the shell can be controlled, its production is easy, it is cheap and combinable with industry. Synthesized microcapsules were characterized by Fourier Transform Infrared Spectroscopy (ATR-FTIR), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy (SEM), optical microscope, UV spectrum, zeta analyzer and contact angle measurements. As a result of the thermal analysis, the core (epoxy) content of the microcapsules was 57% by weight and 60% by the extraction method based on the principle of selective dissolution, and these two values were compatible with each other. The average microcapsule diameter was found as 185 nm. For the first time in the literature, an epoxy-containing microcapsule was added to the thiol-containing coating material and a self-healing coating was prepared. The epoxy-containing microcapsules were artificially cracked and the epoxy resin released from it reacted with the thiol received in the coating. For this reason, it was observed that the artificial scratches formed on the coatings showed good self-healing properties.