Materials Science and Engineering / Malzeme Bilimi ve Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/4719
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Article Citation - WoS: 169Citation - Scopus: 177Thin Film Microextraction: Towards Faster and More Sensitive Microextraction(Elsevier Ltd., 2019) Ölçer, Yekta Arya; Tascon, Marcos; Eroğlu, Ahmet Emin; Boyacı, EzelThin film microextraction (TFME) is an analytical tool that has been proven to be suitable for integrated sampling and sample preparation of a wide variety of routine and on-site applications. Compared to the traditional microextraction techniques, the most important advantage of TFME is its enhanced sensitivity due to the relatively larger extractive phase spread over a larger surface area. The technique, in this way, facilitates fast extraction kinetics and high extractive capacity. Moreover, TFME offers high versatility for device development over classical SPME technologies due to the plethora of available extractive phases, coating methods and geometry options. The goal of this review is to provide a comprehensive summary of the contemporary advances in this exciting field covering novel extractive phases, technological and methodological developments, and relevant cutting-edge applications. Finally, a critical discussion of the future trends on TFME is also presented. (C) 2019 Elsevier B.V. All rights reserved.Correction Citation - Scopus: 1Corrigendum To “hierarchically Porous Polymer Derived Ceramics: a Promising Platform for Multidrug Delivery Systems”[mater. Des. 140(supplement C) (2018) 37–44](Elsevier Ltd., 2018) Ahmetoğlu, Çekdar Vakıf; Zeydanlı, Damla; Özalp, Veli Cengiz; Borsa, Barı Ata; Soraru, Gian DomenicoThe authors regret to inform that The TMTVS ratios for samples were written incorrectly. The true weight ratios for PHMS/LDH/PDMS/TMTVS blends should be as follows: Bio1 = 1/0.055/0.25/0.055, and Bio2 = 1/0.055/1/0.055. The discussion in the study is not affected by this mistype and actually the previous paper [1] cited also in the paper as ref.#44 gives right values for the sample preparation. The authors would like to apologize for the inconvenience caused.Article Citation - WoS: 39Citation - Scopus: 43Tailored Electrospun Fibers From Waste Polystyrene for High Oil Adsorption(Elsevier Ltd., 2018) Isık, Tuğba; Demir, Mustafa MuammerRecent ship accidents that resulted catastrophic oil spills necessitate producing environmentally friendly, costeffective, and large-scale fabrication technology for oil-sorbent materials. Various material systems have been employed to fabricate sorbent materials; however, using fresh material components as adsorbent can lead to a secondary pollution. Therefore, recycling of plastics wastes for the fabrication of adsorbent material could be a wise approach to handle this environmental issue. In this study, foam-expanded polystyrene (f-PS), a commodity polymer used for insulation and packing materials, was electrospun from solution mixture of THF and DMF. Surface and interior porosity were achieved from individual fibers electrospun froma composition of DMF: THF (1:3) at 20-wt% of solid f-PS content. The resulting adsorbents exhibited a considerable hydrophobicity (WCA approximate to 120 degrees) and oleophilicity (CA approximate to 10 degrees), which can selectively adsorb both vegetable and engine oils from polluted waters. The porosity of the fibers has significant effect on the sorption capacity and separation efficiency up to 124 g/g and 99%, respectively. Thus, electrospun mats of the polystyrene wastes offer a promising adsorbent for the remediation of oily wastewaters. (C) 2018 Published by Elsevier B.V.Article Citation - WoS: 30Citation - Scopus: 32Perylene-Embedded Electrospun Ps Fibers for White Light Generation(Elsevier Ltd., 2019) Güner, Tuğrul; Aksoy, Erkan; Demir, Mustafa Muammer; Varlıklı, CananPerylene dyes have been employed in the fabrication of white light due to their superior photophysical properties and relatively easy synthetic methods. However, their molecular aggregation in solid state is one of the main handicaps since it causes deviation in their optical properties and quenches photoluminescence quantum yields (Phi(f)). Investigation of the photophysical properties of a green (PTE), a yellow (PDI) and a new red (DiPhAPDI) emitting perylene derivative in solution, drop-casted films, polystyrene (PS) fibers and PS fibers embedded in poly (dimethyl siloxane) (PDMS) showed that PS:dye fibers prevent aggregation to some extend and allows high Of of dyes. The Of values of PTE, PDI and DiPhAPDI were all higher than 93.0% in solution and 84.8%, 94.3% and 73.6%, respectively in PS:dye fibers. Embedding the fibers in PDMS improved the photostabilities of the dyes two folds compared to their solution phases. The prepared dye containing fibers were combined together into a single PDMS film and utilized as a frequency conversion layer on a blue LED. Fabricated samples were found to show high color rendering index (>= 90), adjustable CCT (7500 K-5000 K), and power efficiency values exceeding 2001m/W depending on the used fiber amount in mass.Article Citation - WoS: 63Citation - Scopus: 65Amidoxime Functionalized Polymers of Intrinsic Microporosity (pim-1) Electrospun Ultrafine Fibers for Rapid Removal of Uranyl Ions From Water(Elsevier Ltd., 2019) Satılmış, Bekir; Isık, Tuğba; Demir, Mustafa Muammer; Uyar, TamerThe Polymers of Intrinsic Microporosity (PIM-1) is considered as one of the most promising polymer candidates for adsorption applications owing to its high surface area and the ability to tailor the functionality for the targeted species. This study reports a facile method for the preparation of amidoxime functionalized PIM-1 fibrous membrane (AF-PIM-FM) by electrospinning technique and its practical use for the extraction of U(VI) ions from aqueous systems via column sorption under continuous flow. Fibrous membrane form of amidoxime functionalized PIM-1 (AF-PIM-FM) was prepared by electrospinning method owing to its excellent processability in dimethylformamide. Bead-free and uniform fibers were obtained as confirmed by SEM imaging and average fiber diameter was 1.69 +/- 0.34 mu m for AF-PIM-FM. In addition, electrospun PIM-1 fibrous membrane (PIM-FM) was prepared as a control group. Structural and thermal characterization of powder and membrane forms of the materials were performed using FT-IR, H-1 NMR, XPS, Elemental analyses, TGA, and DSC. The porosity of the samples was measured by N-2 sorption isotherms confirming amidoxime PIM-1 still maintain their porosity after functionalization. Amidoxime functionality along with membrane structure makes AF-PIM-FM a promising material for uranyl adsorption. First, a comparison between powder and membrane form of amidoxime functionalized PIM-1 was investigated using batch adsorption process. Although membrane form has shown slightly lower adsorption performance in the batch adsorption process, the advantage of using the membrane in column adsorption processes makes membrane form more feasible for real applications. In addition, amidoxime modification enhanced the uranium adsorption ability of PIM-FM up to 20 times. The effect of initial concentration and pH were investigated along with regeneration of the adsorbents. AF-PIM-FM was successfully used for five adsorption-desorption cycles without having any damage on the fibrous structure.Article Citation - WoS: 7Citation - Scopus: 7Increasing Spontaneous Wet Adhesion of Dopa With Gelation Characterized by Epr Spectroscopy(Elsevier Ltd., 2019) Göksel, Yaman; Akdoğan, YaşarThe presence of water molecules around both adhesive materials and surface results in the hydration barriers that weaken adhesion. In nature, mussels attach to various types of surfaces by using 3,4-dihydroxyphenylalanine (DOPA) containing mussel foot proteins. DOPA shows wet adhesive properties before and after contribution in the hydrogel formation. Here, the wet adhesive properties of DOPA modified four armed poly (ethylene glycol) polymer (PEG-(DOPA)(4)) and its hydrogels induced by (IO4)(-) or (Cr2O7)(2-) ions are compared by using electron paramagnetic resonance (EPR) spectroscopy in terms of their surface coverages. In water, spin labeled hydrophobic polystyrene (SL-PS) and hydrophilic silica (SL-SiO2) nanoparticles are prepared, and the percentages of their covered surface values are obtained. Without applying force, the adhesion to SL-PS increases in the order of PEG-(DOPA)(4) < PEG-(DOPA)(4) + (IO4)(-) hydrogel < PEG-(DOPA)(4) + (Cr2O7)(2-) hydrogel with the percentages of surface coverages 65%, 76% and 93%, respectively. Although, neither of PEG-(DOPA)(4) polymer and (IO4)(-) induced PEG-(DOPA)(4) hydrogel adhere to SL-SiO2 nanoparticle spontaneously, (Cr2O7)(2-) induced PEG-(DOPA)(4) hydrogel adhere to SL-SiO2 with a 59% of surface coverage. These results show that gelation mechanisms of DOPA have effect on the spontaneous adhesion of DOPA to the wet surfaces even for the hydrophilic silica surface.Article Citation - WoS: 33Citation - Scopus: 40Preparation of Albumin Nanoparticles in Water-In Liquid Microemulsions(Elsevier Ltd., 2019) Demirkurt, Begüm; Çakan Akdoğan, Gülçin; Akdoğan, YaşarIonic liquids (Its) with a variety of properties have been considered a unique class of solvents. Using ILs in microemulsions as oil substitutes provides environmentally benign media for various applications including nanoparticle synthesis. Here, bovine serum albumin nanoparticles (BSA NPs) widely used in drug delivery studies were prepared in nano-sized water droplets of water-in-IL (W/IL) microemulsion systems. A hydrophobic IL of 1-butyl-3-methylimidazolium hexafluorophosphate (BmimPF(6)) was used as oil component in place of oils (castor oil, olive oil, etc.) and/or conventional organic solvents (cyclohexane, dichloromethane, etc.) in an emulsification method. In order to obtain spherical BSA NPs, high speed homogenizer treatment was applied followed by glutaraldehyde addition. Effects of glutaraldehyde, speed of homogenizer, type of surfactants and compositional fractions of the microemulsion components on the formation of water droplets and/or preparation of BSA NPs were studied using FTIR, EPR, DLS, and SEM techniques. Optimization of these preparation parameters showed that 3 wt% of BSA in a water/Tween 20/BmimPF(6) microemulsion with 20:50:30 wt% yielded similar to 100 nm average sized BSA NPs based on the SEM analysis. Although, water droplet size strongly depends on the water content, BSA nanoparticle size did not show a significant dependency on the water content. On the other hand, surfactant/IL weight ratio is more crucial for obtaining more uniformly size distributed albumin nanoparticles. A significant cellular uptake of BSA NPs prepared in IL based microemulsions with high cell viability showed the potential of this technique in preparation of albumin nanoparticles that can be used also in drug delivery studies. (C) 2019 Elsevier B.V. All rights reserved.Article Citation - WoS: 5Citation - Scopus: 5Effect of Chain Topology on Plasmonic Properties of Pressure Sensor Films Based on Poly(acrylamide) and Au Nanoparticles(Elsevier Ltd., 2019) Topçu, Gökhan; Demir, Mustafa MuammerAu nanoparticles have been recognized as a colorimetric sensing element in polymeric systems because clustering shifts the red color of individual particles into saturated blue due to distinct plasmonic variation. The mechanism of pressure sensing is based on the disintegration of the particle clusters into the individual particles in polymers upon application of pressure. Polymers are usually composed of linear chains that provide a viscoelastic medium for their diffusion. Changing topology of polymer chains from linear to crosslinked under fixed pressure makes a clear change in spectral features of the particles probably due to the hindrance of particle diffusion by the crosslinking points. Therefore, the working range of the sensor films can be increased to higher-pressure values. In this work, polyacrylamide/Au nanoparticle films were prepared by various concentrations of formaldehyde as a crosslinking agent from 0.5 to 5.0 wt %. The initial absorption signal gradually shifts from 690 to 545 nm for linear chains upon application of pressure while shifting goes down to 571 nm for crosslinked ones. The colorimetric change is also examined under humid environments. Contrary to the crosslinking process, humid environment facilitates the diffusion of particles since the chains swell with water molecules that provide a convenient medium for particle diffusion.Article Citation - WoS: 2Citation - Scopus: 2Tuning Thermal Transport in Graphene Via Combinations of Molecular Antiresonances(Elsevier Ltd., 2018) Sevim, Koray; Sevinçli, HaldunWe propose a method to engineer the phonon thermal transport properties of low dimensional systems. The method relies on introducing a predetermined combination of molecular adsorbates, which give rise to antiresonances at frequencies specific to the molecular species. Despite their dissimilar transmission spectra, thermal resistances due to individual molecules remain almost the same for all species. On the other hand, thermal resistance due to combinations of different species are not additive and show large differences depending on the species. Using a toy model, the physics underlying the violation of resistance summation rule is investigated. It is demonstrated that equivalent resistance of two scatterers having the same resistances can be close to the sum of the constituents or ∼ 70% of it depending on the relative positions of the antiresonances. The relative positions of the antiresonances determine the net change in transmission, therefore the equivalent resistance. Since the entire spectrum is involved in phonon spectrum changes in different parts of the spectrum become important. Performing extensive first-principles based computations, we show that these distinctive attributes of phonon transport can be useful to tailor the thermal transport through low dimensional materials, especially for thermoelectric and thermal management applications.Article Citation - WoS: 21Citation - Scopus: 28Non-Iridescent Structural Colors From Uniform-Sized Sio2 Colloids(Elsevier Ltd., 2018) Topçu, Gökhan; Güner, Tuğrul; Demir, Mustafa MuammerStructural colors have recently attracted interest from diverse fields of research due to their ease of fabrication and eco-friendliness. These types of colors are, in principle, achieved by periodically arranged submicron-diameter colloidal particles. The interaction of light with a structure containing long-range ordered colloidal particles leads to coloration; this usually varies depending on the angle of observation (iridescence). However, the majority of the applications demand constant color that is independent of the viewing angle (non-iridescence). In this work, silica colloids were obtained using the Stöber method at different sizes from 150 to 300 nm in an alcoholic dispersion. The casting of the dispersion on a substrate leaves behind a photonic crystal showing a colorful iridescent film. However, centrifugation and redispersion of the SiO2 particles into fresh solvent may cause the formation of small, aggregated silica domains in the new dispersion. The casting of this dispersion allows for the development of photonic glass, presumably due to the accumulation of aggregates showing stable colloidal film independent of viewing angle. Moreover, depending on the size of the silica colloids, non-iridescent photonic glasses with various colors (violet, blue, green, and orange) are obtained.