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Permanent URI for this collectionhttps://hdl.handle.net/20.500.14288/3
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Publication Metadata only Antibacterial silicone-urea/organoclay nanocomposites(Springer, 2009) Department of Chemistry; N/A; N/A; Department of Chemistry; Yılgör, Emel; Nugay, Işık Işıl; Bakan, Murat; Yılgör, İskender; Researcher; Undergraduate Student; Undergraduate Student; Faculty Member; Department of Chemistry; College of Sciences; College of Engineering; College of Engineering; College of Sciences; N/A; N/A; N/A; 24181Montmorillonite modified with distearyldimethyl ammonium chloride (C18-QAC) (Nanofil-15) (NF15) was incorporated into polydimethylsiloxane-urea (silicone-urea, PSU) copolymers. PSU was obtained by the reaction of equimolar amounts of aminopropyl terminated polydimethylsiloxane (PDMS) oligomer (= 3,200 g/mol) and bis(4-isocyanatohexyl) methane (HMDI). A series of PSU/NF15 nanocomposites were prepared by solution blending with organoclay loadings ranging from 0.80 to 9.60% by weight, corresponding to 0.30 to 3.60% C18-QAC. Colloidal dispersions of organophilic clay (NF15) in isopropanol were mixed with the PSU solution in isopropanol and were subjected to ultrasonic treatment. Composite films were obtained by solution casting. FTIR spectroscopy confirmed that the organoclay mainly interacted with the urea groups but not with PDMS. XRD analysis showed that nanocomposites containing up to 6.40% by weight of organoclay had fully exfoliated silicate layers in the polymer matrix, whereas 9.60% loading had an intercalated structure. Physicochemical properties of nanocomposites were determined. PSU/NF15 nanocomposites displayed excellent long-term antibacterial properties against E. coli.Publication Metadata only Motion of single terrylene molecules in confined channels of poly(butadiene)-poly(ethylene oxide) diblock copolymer(Amer Chemical Soc, 2009) N/A; Department of Physics; Department of Chemistry; Yorulmaz, Mustafa; Kiraz, Alper; Demirel, Adem Levent; Master Student; Faculty Member; Faculty Member; Department of Physics; Department of Chemistry; Graduate School of Sciences and Engineering; College of Sciences; College of Sciences; N/A; 22542; 6568The motion of terrylene probe molecules in confined PB channels of an asymmetric PB-PEO diblock copolymer has been investigated by single molecule tracking. The one-dimensional diffusion coefficients were found to be significantly smaller and had a narrower distribution compared to two-dimensional diffusion coefficients in PB. The trajectories of some single molecules showed unusual behavior of directed motion where mean square displacement had a parabolic dependence oil lag time. The likely origin of this behavior is discussed in terms of local variations in the PB channel width and the resulting change in the local density. The results show the effect of nonuniformities and heterogeneities in the channels on the motion of single molecules and demonstrate the sensitivity of single molecule tracking in characterizing self-assembled block copolymer morphologies.Publication Metadata only Interplay between copper nanoparticle size and oxygen vacancy on mg-doped ceria controls partial hydrogenation performance and stability(Amer Chemical Soc, 2021) N/A; N/A; Department of Chemical and Biological Engineering; Zhao, Yuxin; Jalal, Ahsan; Uzun, Alper; PhD Student; PhD Student; Faculty Member; Department of Chemical and Biological Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; College of Engineering; N/A; N/A; 59917A series of CunCeMgOx catalysts with various copper nanoparticle sizes and surface defect densities were synthesized and tested for partial hydrogenation of 1,3-butadiene (1,3-BD). The data demonstrated a reaction pathway involving the dissociation of molecular hydrogen on the peripheral oxygen vacancies (O-v-Cu+) before reacting with 1,3-BD adsorbed on the corresponding Cu+ atoms. Analysis of the performance data indicated that the turnover frequency of these Cu+ sites is approximately five times higher than those of the surface Cu-0 sites. Among the catalysts considered, Cu0.5CeMgOx with the smallest copper nanoparticle size provided a stable performance for at least 15 h time-on-stream, while the others were easily deactivating because of carbon deposition. Furthermore, unlike the conventional copper-based catalysts, the Cu0.3CeMgOx catalyst achieved a complete suppression of total hydrogenation even at space velocities offering a complete 1,3-BD conversion. The findings offer a broad potential for the rational design of noble metal-free, highly selective, and stable copper-based partial hydrogenation catalysts for reactions that are prone to coke formation.Publication Metadata only Platelets to rings: influence of sodium dodecyl sulfate on zn-al layered double hydroxide morphology(Academic Press Inc Elsevier Science, 2012) N/A; Department of Chemistry; Department of Chemistry; Akkaya, Ceren Yılmaz; Ünal, Uğur; Acar, Havva Funda Yağcı; PhD Student; Faculty Member; Faculty Member; Department of Chemistry; Graduate School of Sciences and Engineering; College of Sciences; College of Sciences; N/A; 42079; 178902; 179997In the current study, influence of sodium dodecyl sulfate (SDS) on the crystallization of Zn-Al layered double hydroxide (LDH) was investigated. Depending on the SDS concentration coral-like and for the first time ring-like morphologies were obtained in a urea-hydrolysis method. It was revealed that the surfactant level in the starting solution plays an important role in the morphology. Concentration of surfactant equal to or above the anion exchange capacity of the LDH is influential in creating different morphologies. Another important parameter was the critical micelle concentration (CMC) of the surfactant. Surfactant concentrations well above CMC value resulted in ring-like structures. The crystallization mechanism was discussed.Publication Metadata only Transformation of reduced graphene aerogel-supported atomically dispersed iridium into stable clusters approximated as Ir-6 during ethylene hydrogenation catalysis(Elsevier, 2022) Zhao, Yuxin; Hoffman, Adam S.; Gates, Bruce C.; Bare, Simon R.; Department of Chemistry; Department of Chemical and Biological Engineering; N/A; N/A; N/A; Ünal, Uğur; Uzun, Alper; Öztulum, Samira Fatma Kurtoğlu; Yalçın, Kaan; Çağlayan, Hatice Pelin; Faculty Member; Faculty Member; PhD Student; Master Student; Master Student; Department of Chemistry; Department of Chemical and Biological Engineering; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); College of Sciences; College of Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; 42079; 59917; 384798; N/A; N/ATransformation of atomically dispersed reduced graphene aerogel (rGA)-supported complexes, Ir-I(C2H4)(2)(+), with an iridium loading of 9.9 wt%, to form low-nuclearity clusters was investigated during ethylene hydrogenation catalysis. Continuous-scan X-ray absorption spectra demonstrate the formation of clusters well approximated as Ir-4 during reaction at 100 degrees C in flowing equimolar ethylene and H-2. The Ir-4 clusters transformed into clusters well approximated as Ir 6 when the feed molar ratio was switched to H-2: C2H4 = 2 and remained stable in pure H-2 at 100 degrees C. Catalyst performance data show that hydrogenation activity increased with metal nuclearity in the order of atomically dispersed iridium/rGA << Ir-4/rGA < Ir-6/ rGA. Continuous scan X-ray absorption data, complemented with aberration-corrected scanning transmission electron microscopy images, demonstrate that the supported clusters approximated as Ir-6 are stable even in H-2 at atmospheric pressure and 100 degrees C. These supported iridium clusters are among the ones having the highest metal loadings reported for a supported metal cluster catalyst.Publication Metadata only Polyurethane synthesis revisited: effect of solvent and reaction conditions on prepolymer formation and polymer properties(American Chemical Society (ACS), 2014) N/A; Department of Chemistry; Department of Chemistry; Yıldırım, Armen; Yılgör, Emel; Yılgör, İskender; Master Student; Researcher; Faculty Member; Department of Chemistry; Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of Sciences; College of Sciences; College of Sciences; College of Sciences; College of Sciences; N/A; 40527; 24181N/APublication Metadata only Influence of competitive hydrogen bonding between hard and soft segments on the properties of siloxane and polyether-based segmented copolymers.(Amer Chemical Soc, 1999) Department of Chemistry; Department of Chemistry; N/A; Yılgör, İskender; Burgaz, Engin; Metin, Burak; Yurtsever, İsmail Ersin; Yılgör, Emel; Faculty Member; Undergraduate Student; Undergraduate Student; Faculty Member; Researcher; Department of Chemistry; College of Sciences; College of Sciences; N/A; 24181; 17956; N/A; N/A; 40527N/APublication Metadata only Electroadhesion with application to touchscreens(Royal Soc Chemistry, 2019) Ayyıldız, Mehmet; Persson, Bo N. J.; N/A; Department of Mechanical Engineering; Şirin, Ömer; Başdoğan, Çağatay; PhD Student; Faculty Member; Department of Mechanical Engineering; Graduate School of Sciences and Engineering; College of Engineering; N/A; 125489There is growing interest in touchscreens displaying tactile feedback due to their tremendous potential in consumer electronics. In these systems, the friction between the user's fingerpad and the surface of the touchscreen is modulated to display tactile effects. One of the promising techniques used in this regard is electrostatic actuation. If, for example, an alternating voltage is applied to the conductive layer of a surface capacitive touchscreen, an attractive electrostatic force is generated between the finger and the surface, which results in an increase in frictional forces acting on the finger moving on the surface. By altering the amplitude, frequency, and waveform of this signal, a rich set of tactile effects can be generated on the touchscreen. Despite the ease of implementation and its powerful effect on our tactile sensation, the contact mechanics leading to an increase in friction due to electroadhesion has not been fully understood yet. In this paper, we present experimental results for how the friction between a finger and a touchscreen depends on the electrostatic attraction and the applied normal pressure. The dependency of the finger-touchscreen interaction on the applied voltage and on several other parameters is also investigated using a mean field theory based on multiscale contact mechanics. We present detailed theoretical analysis of how the area of real contact and the friction force depend on contact parameters, and show that it is possible to further augment the friction force, and hence the tactile feedback displayed to the user by carefully choosing those parameters.Publication Metadata only Novel nanostructured composites of silica aerogels with a metal organic framework(Elsevier, 2013) N/A; N/A; Department of Chemical and Biological Engineering; Department of Chemical and Biological Engineering; Ülker, Zeynep; Eruçar, İlknur; Keskin, Seda; Erkey, Can; PhD Student; PhD Student; Faculty Member; Faculty Member; Department of Chemical and Biological Engineering; Koç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM); Graduate School of Sciences and Engineering; Graduate School of Sciences and Engineering; College of Engineering; College of Engineering; 262388; 260094; 40548; 29633Novel nanostructured composites of silica aerogel with Cu-BTC were synthesized using a slightly modified version of the conventional sol-gel method used to synthesize silica aerogels. The composite materials had monolithic structures with blue color consisting of well dispersed microporous domains of Cu-BTC in the mesoporous inorganic silica aerogel network. The Cu-BTC content in the composites ranged from 5 to 30 weight percent and the total surface area of the composites ranged from 1025 to 1138 m(2)/g. The microporosity of the composites increased with the increasing amount of Cu-BTC indicating that the micropores of Cu-BTC were accessible and functional. XRD analysis indicated that Cu-BTC retained its crystal structure in the composite despite being immersed in a solution containing water, ethanol and tetraethylorthosilicate. Additionally, it was observed that increasing Cu-BTC content caused a decrease in the average desorption pore radius with a wider pore size distribution. Nitrogen adsorption isotherms for composites could be predicted using the experimentally obtained pure component isotherm for the silica aerogel, theoretically obtained isotherm for Cu-BTC and the weight fractions of the components within the composite material.Publication Metadata only Vibrational spectra, force constants and quantum chemical calculations of mu-1,3-azide bridged triphenylphosphine complexes of copper(I) and silver (I)(Elsevier, 2022) Güven, Gökçe; Afyon, Semih; Yılmaz, Ayberk; Bölükbaşı, Olcay; N/A; Department of Chemistry; Topçu, Ahmet Umur; Somer, Mehmet Suat; N/A; Faculty Member; Department of Chemistry; N/A; College of Sciences; N/A; 178882The dimeric title compounds [(C6H5)(3)P]Cu-2(N-3)(2) and [C6H5)(3)P]Ag-2(N-3)(2) were synthesized and characterized by FT-Raman and IR spectroscopy. The two phases were not isotypic but possessed approximately the same molecular symmetry which was C-2/2m. The assignment of the modes was supported by quantum chemical DFT calculations coupled with TED (Total Energy Distribution) analyses. The calculated (N-N) force constants for the bridging -(NNN)- groups were directly comparable (f(N-N) = 11.75 (Cu) and 12.19 N cm(-1)(Ag)) and harmonized well with those of the free azide anion in the binary alkali azides. The (N-N) bond orders were obtained based on the calculated force constants (Siebert Bond Order, SBO) and Density-dependent electrostatic and chemical (DDEC6) method yielding SBO = 1.92 (Cu) and 1.96 (Ag) and BO = 2.00 (Cu) and 2.03 (Ag), respectively, indicating the presence of double bonds. The results underlined that the (N-N) force constants and bond orders in the bridging azide units were practically unaffected by the nature of the central metal atoms and that they could be regarded as quasi isolated anions similar to those in the binary azide compounds.