Browsing by Author "Demir M.M."

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Aggregation of fillers blended into random elastomeric networks: Theory and comparison with experiments
(2006) Demir M.M.; Menceloglu Y.Z.; Erman, B.
A theoretical model describing aggregation of filler particles in amorphous elastomers is proposed. The model is based on a counting technique originally used in genome analysis to characterize the size and distribution of overlapping segments randomly placed on a DNA molecule. In the present model, the particles are first assumed to aggregate randomly upon mixing into the elastomer and then-sizes are calculated. The sizes and distributions of aggregates are also studied in the presence of attractive interparticle forces. Results of the proposed model are compared with experimental data on silica-filled end-linked poly(dimethyl-siloxane) networks. Comparison of the theory and experiment shows that the random aggregation assumption where no attractive forces exist between the particles is not valid and a significant attraction between the silica particles is needed in the theory to justify the experimental data obtained using atomic force microscopy. For filler content below 1.45 vol.-%, the model agrees, qualitatively, with experiment and shows the increase in cluster size with increasing amount of filler. It also explains the increase in the dispersion of aggregate sizes with increasing amount of filler. © 2006 WILEY-VCH Verlag GmbH & Co. KGaA.
Challenges in the preparation of optical polymer composites with nanosized pigment particles: A review on recent efforts
(2012) Demir M.M.; Wegner, G.
Blends of nanosized pigment particles and polymers are widely believed to offer the potential for the design of novel or at least improved materials. This review critically evaluates the recent literature with regard to the following issues: (a) why and how does the size of the particles matter, (b) what are the requirements to create compatibility between amorphous polymers and nanoparticles, (c) carbon allotropes as nanosized pigments, (d) bulk polymerization of monomer/pigment mixtures, (e) interaction of growing chains with the particles in the polymerization, (f) depletion flocculation as a mechanism to counteract homogeneous distribution of the particles in the polymer matrix and ways to suppress the undesirable flocculation, and (g) optical properties of the blends as well as methods of optical characterization. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Characterization of Sb scaling and fluids in saline geothermal power plants: A case study for Germencik Region (Büyük Menderes Graben, Turkey)
(Elsevier Ltd, 2021) Tonkul S.; Baba A.; Demir M.M.; Regenspurg, S.
Turkey is located on the seismically active Alpine-Himalayan belt. Although tectonic activity causes seismicity in the Anatolian plate, it also constitutes an important geothermal energy resource. Today, geothermal energy production is heavily concentrated in Turkey's Western Anatolia region. Graben systems in this region are very suitable for geothermal resources. The Büyük Menderes Graben (BMG) is an area of complex geology with active tectonics and high geothermal potential power. Germencik (Aydın) is located in the BMG, where the geothermal waters include mainly Na-Cl-HCO3 water types. This study examined the stibnite scaling formed in the preheater system of the Germencik Geothermal Field (GGF). The formation of the stibnite scaling on the preheater system dramatically reduces the energy harvesting of the GGF. Considering the stibnite scaling in the surface equipment, the optimum reinjection temperature was determined as 95 °C to prevent stibnite scaling in the GGF. © 2021 Elsevier Ltd
Color-tunable all-inorganic CsPbBr3 Perovskites Nanoplatelet Films for Photovoltaic Devices
(American Chemical Society, 2019) Ozcan M.; Ozen S.; Topcu G.; Demir M.M.; Sahin, H.
Herein, we demonstrate a novel coating approach to fabricate CsPbBr3 perovskite nanoplatelet film with heat-free process via electrospraying from precursor solution. A detailed study is carried out to determine the effect of various parameters such as ligand concentration, electric field, flow rate, etc. on the optical properties. By controlling the volume ratios of the oleylamine (OAm) and oleic acid (OA), the coalescing and thickness of the resulting nanoplatelets can be readily tuned that results in control over emission in the range of 100 nm without any antisolvent crystallization or heating processes. The varying electrical field and flow rate was found as inefficient on the emission characteristics of the films. In addition, the crystal films were obtained under ambient conditions on the ITO coated glass surfaces as in the desired pattern. As a result, we demonstrated a facile and reproducible way of synthesizing and coating of CsPbBr3 perovskite nanoplatelets which is suitable for large-scale production. In this method, the ability of tuning the degree of quantum confinement for perovskite nanoplatelets is promising approach for the one-step fabrication of crystal films that may enable the use in optoelectronics. Copyright © 2019 American Chemical Society.
Composites of reactive silica nanoparticles and poly(glycidyl methacrylate) with linear and crosslinked chains by in situ bulk polymerization
(2010) Demir M.M.; Altn B.; Özçelik, S.
Composites of poly(glycidyl methacrylate) (PGMA) and L-lysine-coated silica nanoparticles with varying contents were prepared by in situ bulk polymerization using benzoyl peroxide (BPO) as free radical initiator. Silica nanoparticles covered by L-lysine molecules were synthesized using emulsion method. Dynamic light scattering measurements confirmed that the particles are highly monodisperse with the diameter of 10 nm and free of aggregates in the monomer (glycidyl methacrylate, GMA). Upon polymerization of the homogeneous particle/monomer dispersion, aggregates of individual silica nanoparticles are observed by tapping mode atomic force microscope (AFM). Amine and/or carboxylic acid sites on particle surface covalently react with the oxirane groups of the polymer backbone. The aggregation was substantially suppressed by using a difunctional comonomer divinyl benzene (DVB) in polymerization. A three-dimensional polymer network, P(GMA-DVB), forms throughout the system. This structure leads to significant progress in particle dispersion, therefore in physical properties of the resulting composite. We demonstrated that the composites prepared by crosslinked chains are thermally more stable and mechanically stiffer than those prepared by linear ones. © 2010 Koninklijke Brill NV, Leiden.
Controlling spontaneous emission of CdSe nanoparticles dispersed in electrospun fibers of polycarbonate urethane
(2009) Demir M.M.; Soyal D.; Ünlü C.; Kuş M.; Özçelik, S.
Luminescent fibrous composite films consisting of submicrometer diameter fibers were prepared by electrospinning of segmented polycarbonate urethane (PCU) in dimethyl formamide and tri-n-octylphosphine oxide (TOPO)-capped CdSe nanocrystals (5 nm in diameter) in toluene. Using a pair of conductive electrodes separated with an air gap, we successfully produced randomly deposited and uniaxially aligned electrospun fibers. The surface structure of the electrospun fibers was studied using atomic force microscopy (AFM) and was compared to the corresponding film prepared by casting. In cast film, tapping mode AFM imaging suggests that hard urethane segments organize into rodlike morphology dispersed in soft polycarbonate. When PCU/CdSe dispersions were subjected to electrospinning, copolymer domains were forced to arrange into lamella along the fiber axis due to elongational flow and high stretching. Molecular orientation in the domains of the composite fibers was confirmed by polarized infrared spectroscopy. We demonstrated that formation of the oriented domains by electrospinning develops a hierarchical structure, which consequently modifies spectral properties because new multiple sharp lines appeared in the photoluminescence (PL) spectra of the fibers. In contrast to randomly deposited fibers, the PL intensity of uniaxially aligned fibers was found to be angle dependent. We propose that the elongated internal structure within the fibers controls the spontaneous emission of CdSe nanoparticles dispersed throughout the electrospun mat. A discussion on the nature of the controlled spontaneous emission is provided. © 2009 American Chemical Society.
Correction to: Enhanced light–matter interaction in a hybrid photonic–plasmonic cavity (Applied Physics A, (2021), 127, 12, (907), 10.1007/s00339-021-05071-x)
(Springer Science and Business Media Deutschland GmbH, 2022) Gökbulut B.; Inanç A.; Topcu G.; Ozcelik S.; Demir M.M.; Inci, M.N.
In this article the statement in the Funding information section was incorrect. The correct Funding information is as follows. ‘Dr Belkıs Gökbulut acknowledges TUBITAK for the financial support provided under Contract Number 120F323’. © The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature 2022.
CsPbBr3 perovskites: Theoretical and experimental investigation on water-assisted transition from nanowire formation to degradation
(American Physical Society, 2018) Akbali B.; Topcu G.; Guner T.; Ozcan M.; Demir M.M.; Sahin, H.
Recent advances in colloidal synthesis methods have led to an increased research focus on halide perovskites. Due to the highly ionic crystal structure of perovskite materials, a stability issue pops up, especially against polar solvents such as water. In this study, we investigate water-driven structural evolution of CsPbBr3 by performing experiments and state-of-the-art first-principles calculations. It is seen that while an optical image shows the gradual degradation of the yellowish CsPbBr3 structure under daylight, UV illumination reveals that the degradation of crystals takes place in two steps: transition from a blue-emitting to green-emitting structure and and then a transition from a green-emitting phase to complete degradation. We found that as-synthesized CsPbBr3 nanowires (NWs) emit blue light under a 254 nm UV source. Before the degradation, first, CsPbBr3 NWs undergo a water-driven structural transition to form large bundles. It is also seen that formation of such bundles provides longer-term environmental stability. In addition theoretical calculations revealed the strength of the interaction of water molecules with ligands and surfaces of CsPbBr3 and provide an atomistic-level explanation to a transition from ligand-covered NWs to bundle formation. Further interaction of green-light-emitting bundles with water causes complete degradation of CsPbBr3 and the photoluminescence signal is entirely quenched. Moreover, Raman and x-ray-diffraction measurements revealed that completely degraded regions are decomposed to PbBr2 and CsBr precursors. We believe that the findings of this study may provide further insight into the degradation mechanism of CsPbBr3 perovskite by water. © 2018 American Physical Society.
Development of molecularly imprinted polymers (MIPs) as a solid phase extraction (SPE) sorbent for the determination of ibuprofen in water
(Royal Society of Chemistry, 2017) Olcer Y.A.; Demirkurt M.; Demir M.M.; Eroglu, A.E.
Ibuprofen is a well-known endocrine disrupter. In this study, highly selective molecularly imprinted polymers (MIPs) with different morphologies were synthesized via precipitation and bulk polymerization of methacrylic acid (MAA) and trimethylolpropane trimethacrylate (TRIM) in the presence of ibuprofen as a template. Non-imprinted polymers (NIPs) were also synthesized via the same procedure in the absence of ibuprofen. Spherical and monolithic MIPs were obtained using different experimental conditions, and the spherical MIP was shown to have better sorption towards ibuprofen. The optimum sample pH, sorbent amount, sample volume, and sorption time were determined to be 8.0, 25.0 mg, 10.0 mL, and 30.0 min, respectively. A methanol water mixture (MeOH:H2O, 80:20, pH 3.0) was employed as an eluent with >97% (±0.8, n = 3) desorption. The MIP demonstrated high selectivity towards ibuprofen in the presence of naproxen and ketoprofen. The validity of the proposed method was checked via spike recovery tests using drinking and tap water samples. The method worked efficiently for both water types, resulting in the recoveries of 97.2% (±0.3, n = 3) and 97.7% (±0.2, n = 3). © 2017 The Royal Society of Chemistry.
Dimensions of polystyrene particles deposited on mica from dilute cyclohexane solution at different temperatures
(2002) Demir M.M.; Erman, B.
Using atomic force microscopy, the height, diameter, and volume of polystyrene particles deposited on mica from dilute cyclohexane solution at different temperatures are determined. Dimensions exhibit a strong temperature dependence. The heights of the deposited particles are only a few atomic diameters, the major dimension being parallel to the mica surface. The number of single polystyrene molecules in a deposited particle cannot be determined directly by atomic force microscopy. However, the maximum number of molecules that may be present in a particle may be estimated. Below 35 °C, the particles possibly consist of single collapsed molecules. This number increases with temperature and becomes as large as about 30 molecules per particle at 80 °C. The volume occupied by a single chain in solvent is calculated as a function of temperature and compared with observed volumes of dry particles on mica. A linear relationship is observed between single chain volumes in solvent and corresponding particle volumes on mica. On the average, the volume of a single chain in solution is 10 times the volume of a dry particle at the corresponding temperature. Fluctuations of chain volumes that are dominant in solution are also present in the volumes of particles deposited and dried on mica.
Effect of filler amount on thermoelastic properties of poly(dimethylsiloxane) networks
(Elsevier BV, 2005) Demir M.M.; Menceloglu Y.Z.; Erman, B.
End-linked poly(dimethylsiloxane) (PDMS) networks were prepared in the presence of fumed silica particles with hydroxyl groups at their surfaces. The silica particles were introduced into the polymer solution prior to end-linking. Hydroxyl ended PDMS chains were end-linked via the tetra functional crosslinker, tetraethoxysilane. The filler content varied in the range 0-5 wt%. Atomic Force Microscopy was used to image and characterize the silica particles. Swelling, stress-strain and thermoelasticity experiments were performed. The temperature coefficient and the energetic part of the force in uniaxial extension are found to increase with increasing silica amount. This observation is ascribed to effects contributed possibly by the adsorption layer around the silica particles. © 2005 Elsevier Ltd. All rights reserved.
Effect of high salinity and temperature on water–volcanic rock interaction
(Springer Science and Business Media Deutschland GmbH, 2021) Gören A.Y.; Topcu G.; Demir M.M.; Baba, A.
In order to understand the processes occurring in natural hydrothermal systems, it was carried out a series of water–volcanic rock interaction studies in the laboratory and an intermediate volcanic rock samples from geothermal production wells in Tuzla geothermal field (TGF) in western Turkey. A high-pressure autoclave was used to conduct water–rock interaction experiments under similar conditions of the field. Rainwater and seawater were treated with volcanic rocks at 140 °C (reservoir temperature) and 4.5 bar pressure. The change in the ionic content of the resulting fluids was examined in terms of the type of volcanic rocks and mineral saturation index. The results indicate that talc and diopside minerals in geothermal systems may cause scaling at high temperatures depending on the geothermal fluid and pH. © 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
Electrospinning of polyurethane fibers
(Elsevier BV, 2002) Demir M.M.; Yilgor I.; Yilgor E.; Erman, B.
A segmented polyurethaneurea based on poly(tetramethylene oxide)glycol, a cycloaliphatic diisocyanate and an unsymmetrical diamine were prepared. Urea content of the copolymer was 35 wt%. Electrospinning behavior of this elastomeric polyurethaneurea copolymer in solution was studied. The effects of electrical field, temperature, conductivity and viscosity of the solution on the electrospinning process and morphology and property of the fibers obtained were investigated. Results of observations made by optical microscope, atomic force microscope and scanning electron microscope were interpreted and compared with literature data available on the electrospinning behavior of other polymeric systems. © 2002 Elsevier Science Ltd. All rights reserved.
Electrospun polystyrene fibers knitted around imprinted acrylate microspheres as sorbent for paraben derivatives
(Elsevier B.V., 2018) Demirkurt M.; Olcer Y.A.; Demir M.M.; Eroglu, A.E.
Parabens are used as antimicrobial preservatives in food, cosmetic products and pharmaceuticals regardless of their endocrine disrupting effect. In this study, highly selective molecular imprinted polymers (MIPs) were synthesized in submicron-sizes and converted to an SPME fiber coating through electrospinning process in order to determine parabens in water samples. Conversion of MIP to a fiber is achieved via creation of spacial knitting around MIP by polystyrene. The selectivity and extraction ability of the fibers were compared with the commercial fibers and the corresponding non-imprinted polymer (NIP) coated fiber. The coated fiber showed better extraction ability among them. Also, the results revealed that the fiber has better selectivity for benzyl paraben and the other structurally-related compounds, such as methyl and propyl paraben. Extraction efficiency of prepared fibers for three parabens has been tested by spiking bottled, tap and sea water samples. The recoveries changed between 92.2 ± 0.8 and 99.8 ± 0.1 for three different water types. This method could be used for selective and sensitive determination of parabens in aqueous samples. © 2018 Elsevier B.V.
Enhanced light–matter interaction in a hybrid photonic–plasmonic cavity
(Springer Science and Business Media Deutschland GmbH, 2021) Gökbulut B.; Inanç A.; Topcu G.; Ozcelik S.; Demir M.M.; Inci, M.N.
Strongly concentrated optical fields around a metal nanoparticle in the close vicinity of a dipole noticeably facilitate dramatic changes in the localized density of states due to hybrid photonic–plasmonic mode couplings as compared to that of the pure cavity mode fields. Significant variations of the field intensity in the presence of the metal nanoparticle elucidate enhanced light–matter interaction in a hybrid structure. The enhancement factor of the light–matter interaction is studied through the single-atom cooperativity parameter, which is directly proportional to the ratio of the fluorescence lifetimes of the off-resonant and on-resonant emission. A compact and cost-effective hybrid device, which includes a microfiber cavity, supporting whispering gallery modes, and a well-defined solid nanostructure, consisting of a gold nanoparticle core, overcoated by a silica shell, and decorated with CdS/CdSe quantum dots, is demonstrated to offer an outstanding potential for the enhancement of light–matter interaction. Surface plasmons of a gold nanoparticle, placed inside a hollow cylindrical nanostructure at the surface of a microfiber, are activated upon excitation of the dipoles of the quantum emitters, which are on-resonance with the whispering gallery mode. Time-resolved experiments demonstrate that the single-atom cooperativity parameter of the quantum dots is enhanced by a factor of about 4.8 in the presence of the gold nanoparticle being simultaneously in strong interaction with the cavity mode field and the metal nanoparticle’s surface plasmons. © 2021, The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.
Enhanced Spontaneous Emission Rate in a Low- Q Hybrid Photonic-Plasmonic Nanoresonator
(American Chemical Society, 2019) Gökbulut B.; Inanç A.; Topcu G.; Unluturk S.S.; Ozcelik S.; Demir M.M.; Inci, M.N.
In this paper, CdTe quantum dots (QDs)-doped single electrospun polymer nanofibers are partially coated with gold nanoparticles to form distinct hybrid photonic-plasmonic nanoresonators to investigate the critical role of the cavity-confined hybrid mode on the modification of the spontaneous emission dynamics of the fluorescent emitters in low-Q photonic cavities. A total enhancement factor of 11.2 is measured via a time-resolved experimental technique, which shows that there is an increase of about three times in the spontaneous emission rate for the QDs-doped gold nanoparticle-decorated nanofibers as they are compared with those uncoated ones. The physical mechanism affecting the spontaneous emission rate of the encapsulated QDs in such a hybrid photonic-plasmonic nanoresonator is explained to be due to regeneration of the mode field in the nanofiber cavity upon the interaction of the dipoles with the surface plasmons of distinctive gold nanoparticles that surround the outer surface of the nanofiber. Copyright © 2019 American Chemical Society.
Experimental and first-principles investigation of Cr-driven color change in cesium lead halide perovskites
(American Institute of Physics Inc., 2019) Ozen S.; Guner T.; Topcu G.; Ozcan M.; Demir M.M.; Sahin, H.
Herein, we report room temperature Cr-doping for all-inorganic perovskites that have attracted great attention in recent years due to their extraordinary optical properties, low cost, and ease of synthesis. Incorporation of Cr 3 + ions into the perovskite crystal lattices is achieved by following a facile route involving an antisolvent recrystallization method at room temperature. It is shown that both Cr-doping and formation of crystals in the CsPbBr x Cl 3 - x phase are provided by increasing the concentration of the CrCl 3 solution. It is also observed that the doping procedure leads to the emergence of three types of distinctive peaks in the PL spectrum originating from CsPbBr x Cl 3 - x domains (476-427 nm), Cr-strained host lattices (515 nm), and midgap states formed by Cr dopants (675-775 nm). It is also found that the Cr-doped perovskites emitting a dark violaceous color change their color to white with a high color rendering index (88) in 30-day time intervals. Easy-tunable optical properties of all-inorganic Cs perovskites indicate their great potential for future optoelectronic device applications. © 2019 Author(s).
Fabrication of polymer nanofiber-conducting polymer fabric and noncontact motion sensing platform
(Trans Tech Publications Ltd, 2018) Mutlu M.U.; Akin O.; Demir M.M.; Yildiz, Ü.H.
Conductive polymer-electrospun polymer nanofiber network was combined to host iron oxide nanoparticles providing micrometer thick sensing interface. The sensor has fabricated as freestanding fabric exhibiting 10 to 100 KOhm base resistivity upon bias applied. The moving object has been sensed through the electrostatic interactions between fibers and object. The sensing range has been found to be 1-5 cm above the surface of fabric. By the controlled combination of conductive polymers electrospun polymer nanofibers effective device miniaturization has been provided without loss of performance. The noncontact motion sensor platform has unique flexibility and light weight holding a potential for wearable sensor technology. © 2018 Trans Tech Publications, Switzerland.
Formation of pseudoisocyanine J-aggregates in polyvinyl alcohol fibers by electrospinning
(American Chemical Society, 2009) Demir M.M.; Özen B.; Özçelik, S.
Submicrometer diameter, light emitting fibers of polyvinyl alcohol) (PVA) doped with pseudoisocyanine (l,1'-diethyl-2,2'-cyanine bromide, PIC) dye were prepared by electrospinning. A horizontal setup was employed with a stationary collector consisting of two parallel-positioned metal strips separated by a void gap. Formation of uniaxially aligned and randomly deposited fibers in electrospun films was confirmed by microscopy. Photoluminescence (PL) spectroscopy is used to evaluate spectral properties of both types of fibers doped with PIC. While PIC molecules were individually dispersed in PVA solution, they assemble into J-aggregates upon electrospinning when the weight fraction of PIC molecules is above 2.5 wt %. The formation of J-aggregates was observed in both randomly deposited and uniaxially aligned electrospun fibers. Moreover, the fibers aligned uniaxially showed a high degree of polarized emission (PL|/PL⊥ = 10), arising from the orientation of J-aggregates along the fiber axis. On the other hand, isotropic emission of J-aggregates was observed from the fibers deposited randomly. As a conclusion, electrospinning was found to be an efficient and a practical method to form highly oriented J-aggregates dispersed into polymer fibers. To the best of our knowledge, it is the first time formation of J-aggregates (a bottom-up approach) and electrospinning (a topdown approach) is successfully combined. © 2009 American Chemical Society.
Geological and hydrogeochemical properties of geothermal systems in the southeastern region of Turkey
(Elsevier Ltd, 2019) Baba A.; Şaroğlu F.; Akkuş I.; Özel N.; Yeşilnacar M.İ.; Nalbantçılar M.T.; Demir M.M.; Gökçen G.; Arslan Ş.; Dursun N.; Uzelli T.; Yazdani, H.
The Anatolia region is one of the most seismically active regions in the world. It has a considerably high level of geothermal energy potential thanks to its geological and tectonic settings. The Southeastern Anatolia Region (GAP) is located in the south of Bitlis-Zagros Suture Zone (BZSZ) which is in the Arabian foreland. During the neotectonic period, the folded structures have been developed under the influence of tectonic compression from the Upper Miocene in the GAP Region where it is closely related to active tectonics. These tectonic activities produce more geothermal resources. Few studies have been carried out in this region for geothermal energy. Limited portions of the geothermal resources have been used both for thermal tourism and greenhouses in the GAP region. The aim of this study is to determine geological, tectonic and hydrogeochemical properties of a geothermal system in the GAP Region. The result indicates that the surface temperatures of geothermal fluids are from 20 to 84.5 °C A large number of abandoned oil wells, whose temperature reaches 140 °C, are found in the region. Also, hydrogeochemical results show that deep circulated geothermal fluids are enriched with Na-Cl and shallow geothermal system fluids have Na−HCO3 and Ca-SO4 characters because of cold water mixing and water-rock interaction. Cold waters are generally of Ca-Mg−HCO3 and Ca−HCO3 type. Cation geothermometers were used for determining reservoir temperature of the geothermal resources in the region. The results show that the reservoir temperature of these geothermal resources ranges from 50 °C to 200 °C. The isotope data (oxygen-18, deuterium and tritium) suggests that geothermal fluid is formed by local recharge and deep circulation. © 2018 Elsevier Ltd