Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 7Citation - Scopus: 7Investigating the Effects of Pa66 Electrospun Nanofibers Layered Within an Adhesive Composite Joint Fabricated Under Autoclave Curing(American Chemical Society, 2023) Barışık, Murat; Aktaş, Engin; Tanoğlu, Metin; Esenoğlu, Gözde; Yeke, Melisa; Nuhoğlu, Kaan; Türkdoğan, Ceren; Martin, Seçkin; Aktaş, Engin; Dehneliler, Serkan; Gürbüz, Ahmet Ayberk; İriş, Mehmet Erdem; 03.10. Department of Mechanical Engineering; 03.03. Department of Civil Engineering; 01. Izmir Institute of Technology; 03. Faculty of EngineeringEnhancing the performance of adhesively joined composite components is crucial for various industrial applications. In this study, polyamide 66 (PA66) nanofibers produced by electrospinning were coated on unidirectional carbon/epoxy prepregs to increase the bond strength of the composites. Carbon/epoxy prepregs with/without PA66 nanofiber coating on the bonding region were fabricated using the autoclave, which is often used in the aerospace industry. The single lap shear Charpy impact energy and Mode-I fracture toughness tests were employed to examine the effects of PA66 nanofibers on the mechanical properties of the joint region. Scanning electron microscopy (SEM) was used to investigate the nanofiber morphology and fracture modes. The thermal characteristics of Polyamide 66 nanofibers were explored by using differential scanning calorimetry (DSC). We observed that the electrospun PA66 nanofiber coating on the prepreg surfaces substantially improves the joint strength. Results revealed that the single lap shear and Charpy impact strength values of the composite joint are increased by about 79 and 24%, respectively, by coating PA66 nanofibers onto the joining region. The results also showed that by coating PA66 nanofibers, the Mode-I fracture toughness value was improved by about 107% while the glass transition temperature remained constant.Article Citation - WoS: 8Citation - Scopus: 10Spray Analysis of Biodiesels Derived From Various Biomass Resources in a Constant Volume Spray Chamber(American Chemical Society, 2022) Rodriguez, Alvaro Diez; Özkol, Ünver; Yıldız, Güray; Özkol, Ünver; 03.10. Department of Mechanical Engineering; 03.06. Department of Energy Systems Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyThis research aimed to analyze the spray characteristics of various biodiesels, which have rarely been investigated in terms of spray analysis in the literature compared to fossil diesel. For this purpose, four different methyl ester-type biodiesels were produced from canola, corn, cottonseed, and sunflower oils. These feedstocks were selected due to their wide availability in Turkey and being among the significant resources for biodiesel production. Measured physical properties of biodiesel samples showed that biodiesel fuels had, on average, 1.7 to 1.9 times higher viscosities, 5.3 to 6.6% larger densities, and 37 to 39.1% higher contact angle values than the reference diesel fuel. Spray characteristics of all fuels were experimentally examined in a constant volume spray chamber under chamber pressures of 0, 5, 10, and 15 bar and injection pressures of 600, 800, and 1000 bar. All tested biodiesels performed, on average, 3 to 20% longer spray penetration lengths, 5 to 30% narrower spray cone angles, and 5-18% lesser spray areas than the reference diesel fuel under chamber pressures of 5 and 10 bar. No significant differences occurred at 15 bar ambient pressure between biodiesels and diesel. In addition, analytical and empirical predictions showed that biodiesels had around 21.2-35.1% larger SMD values and approximately 7% lower air entrainment.Article Citation - WoS: 16Citation - Scopus: 16Slip Effects on Ionic Current of Viscoelectric Electroviscous Flows Through Different Length Nanofluidic Channels(American Chemical Society, 2020) Şen, Tümcan; Şen, Tümcan; Barışık, Murat; Barışık, Murat; 01. Izmir Institute of Technology; 03.10. Department of Mechanical Engineering; 03. Faculty of EngineeringThe pressure driven slip flow of an electrolyte solution is studied through different nanofluidic channel lengths at varying salt concentrations. The viscous-thickening due to the electrostatic interactions within the electric double layer and the reverse ionic transport due to the streaming potential are developed. The influence of the Navier slip boundary condition is described under both electroviscous and viscoelectric effects with a surface charge regulation (CR) model while the observed behavior is compared and validated with molecular dynamic (MD) calculations from multiple studies. Results show that electroviscous and viscoelectric effects decrease transport. Earlier studies at the no slip boundary presented an increase of ionic current by increasing salt concentration and decreasing channel length. In contrast, our study found that the ionic current occurred almost independent of both salt concentration and channel length, except for very short channels and very low salt concentrations, when electroviscous and viscoelectric effects were considered. In the case of the constant slip length condition, ionic conduction was enhanced, but velocity slip developing on surfaces showed significant variation based on the salt concentration and channel length. This is due to the natural CR behavior enhancing the surface charge and consequential near surface electrohydrodynamics as a result of increase in salt concentration and/or decrease of channel length. Considering that the electroviscous effect alone creates up to 70% lower velocity slips than Poiseuille flow predictions, while further including the viscoelectric effect, results in an almost no-slip condition at high salt concentrations and/or short channels. As a result, the ionic current of a viscoelectric electroviscous slip flow is found to be equal to 1/3 of an electroviscous slip flow and to decrease with a decrease in the channel length.Article Citation - WoS: 32Citation - Scopus: 34Pore Size and Porosity Dependent Zeta Potentials of Mesoporous Silica Nanoparticles(American Chemical Society, 2020) Yakın, Fetiye Esin; Şen, Tümcan; Barışık, Murat; Barışık, Murat; Şen, Tümcan; 01. Izmir Institute of Technology; 03.10. Department of Mechanical Engineering; 03. Faculty of EngineeringMesoporous silica nanoparticles (MSNPs) are synthesized in the various forms of porous structures according to an application's needs, while their zeta potentials play a major role in their function. We show that variation in pore size and/or porosity yields a substantial decrease in MSNP zeta potential up to 25% lower than the theoretical zeta potential predictions for a flat surface at the corresponding ionic conditions in moderate pH range. By considering surface chemistry as a function of local ionic conditions (charge regulation), we calculated local zeta potentials around the MSNP which showed variation between pore openings and solid surfaces. Through a systematic study, we evaluated an average three-dimensional zeta potential for MSNPs with various conditions, based on the ratio of the area covered by pore openings to the rest of the MSNP surface area as a function of three-dimensional porosity and pore size. Results show that the high overlap of ionic layers inside the pores creates electric potentials close to zeta potential of the remaining surface, but large pore size and/or high ionic salt concentration yields divergence. We characterized the variation of MSNP zeta potential in terms of porosity (epsilon(3D)), pore size (D-pore), and ionic condition quantified by Debye length (lambda) and obtained unified behavior as a function of the nondimensional group of epsilon(3D)(D-pore/lambda). For epsilon(3D)(D-pore/lambda) < 0.01, MSNP zeta potential remains similar to flat plate predictions, but it decreases by increasing epsilon(3D)(D-pore/lambda) value. The influence of pore entrances on surface zeta potential increases nonlinearly by the increase of porosity and/or decrease of EDL overlap, similar to a change of area to volume ratio. The current findings are important for the understanding and further control of mesoporous particle transport in various promising and groundbreaking applications such as targeted drug delivery.Article Citation - WoS: 53Citation - Scopus: 59Roughness Effects on the Surface Charge Properties of Silica Nanoparticles(American Chemical Society, 2020) Alan, B. Öykü; Barışık, Murat; Barışık, Murat; Özçelik, H. Gökberk; 03.10. Department of Mechanical Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyThe surface charge property of silica nanoparticles plays a key role in their function. Previous studies assumed surface charge as a homogeneously distributed constant material property, independent of the nanoparticle size and surface condition. Instead, this study considered surface chemistry as a function of local ionic conditions (Charge Regulation) to calculate the local surface charges around a rough nanoparticle, as an extension to our earlier study (J. Phys. Chem. C 2014, 118 (4), 1836-1842). For the current surface heterogeneity in the form of concave and convex circles, the surface charge showed a distinct local variation: decrease due to the electrical double layer (EDL) overlap in the valleys and increase due to curvature effects on the hills of the surface structure. The average of local surface charges decreased with the decrease of the roughness size (D-R), depending on the particle size (D-P) and pH. We characterized the variation of the average surface charge by a nondimensional group we formed as a measure for the EDL overlap and curvature effects [(D-R/lambda) x (D-R/D-P)]. Based on this, we devised a phenomenological model as an extension to the existing flat surface theory, which can successfully predict the average surface charge around a rough/patterned nanoparticle as a function of the particle size, roughness size, and pH.Article Citation - WoS: 17Citation - Scopus: 17Monitoring the Doping and Diffusion Characteristics of Mn Dopants in Cesium Lead Halide Perovskites(American Chemical Society, 2018) Güner, Tuğrul; Şahin, Hasan; Akbalı, Barış; Demir, Mustafa Muammer; Özcan, Mehmet; Topçu, Gökhan; Demir, Mustafa Muammer; Şahin, Hasan; 04.04. Department of Photonics; 03.09. Department of Materials Science and Engineering; 03. Faculty of Engineering; 04. Faculty of Science; 01. Izmir Institute of TechnologyCesium lead perovskites, in the form of CsPbX3 or Cs4PbX6, have been widely used for various optoelectronic applications due to their exceptionally good optical properties. In this study, the effect of Mn doping on the structural and optical properties of cesium lead halide perovskite crystals are investigated from both experimental and theoretical points of view. It is found that adding MnCl2 during the synthesis not only leads to a Mn-driven structural phase transition from Cs4PbBr6 to CsPbCl3 but also triggers the Br- to Cl- halide exchange. On the other hand, it is observed that, under UV illumination, the color of Mn-doped crystals changes from orange to blue in approximately 195 h. While the intensity of Mn-originated photoluminescence emission exponentially decays in time, the intensity of CsPbCl3-originated emission remains unchanged. In addition, diffusive motion of Mn ions results in both a growing population of MnO2 at the surface and transition of the host into a cesium-rich Cs4PbCl6 phase.Article Citation - WoS: 42Citation - Scopus: 43Well-Defined Cholesterol Polymers With Ph-Controlled Membrane Switching Activity(American Chemical Society, 2012) Sevimli, Sema; Bulmuş Zareie, Volga; Zareie, Hadi M.; Bulmuş, Volga; 03.01. Department of Bioengineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyCholesterol has been used as an effective component of therapeutic delivery systems because of its ability to cross cellular membranes. Considering this, well-defined copolymers of methacrylic acid and cholesteryl methacrylate, poly(methacrylic acid-co-cholesteryl methacrylate) P(MAA-co-CMA), were generated as potential delivery system components for pH-controlled intracellular delivery of therapeutics. Statistical copolymers with varying cholesterol contents (2, 4, and 8 mol %) were synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization. Dynamic light scattering (DLS) analysis showed that the hydrodynamic diameters of the copolymers in aqueous solutions ranged from 5 ± 0.3 to 7 ± 0.4 nm for the copolymers having 2 and 4 mol % CMA and 8 ± 1.1 to 13 ± 1.9 nm for the copolymer having 8 mol % CMA with increasing pH (pH 4.5-7.4). Atomic force microscopy (AFM) analysis revealed that the copolymer having 8 mol % CMA formed supramolecular assemblies while the copolymers having 2 and 4 mol % CMA existed as unimers in aqueous solution. The pH-responsive behavior of the copolymers was investigated via UV-visible spectroscopy revealing phase transitions at pH 3.9 for 2 mol % CMA, pH 4.7 for 4 mol % CMA, and pH 5.4 for 8 mol % CMA. Lipid bilayers and liposomes as models for cellular membranes were generated to probe their interactions with the synthesized copolymers. The interactions were determined in a pH-dependent manner (at pH 5.0 and 7.4) using surface plasmon resonance (SPR) spectroscopy and liposome leakage assay. Both the SPR analyses and liposome leakage assays indicated that the copolymer containing 2 mol % CMA displayed the greatest polymer-lipid interactions at pH 5.0, presenting the highest binding ability to the lipid bilayer surfaces, and also demonstrating the highest membrane destabilization activity. CellTiter-Blue assay showed that the copolymers did not affect the cell viability up to 30 μM over a period of 72 h. © 2012 American Chemical Society.Article Citation - WoS: 22Citation - Scopus: 28Mechanical Interlocking Between Porous Electrospun Polystyrene Fibers and an Epoxy Matrix(American Chemical Society, 2014) Demir, Mustafa Muammer; Horzum, Nesrin; Taşdemirci, Alper; Turan, Ali Kıvanç; Güden, Mustafa; Güden, Mustafa; Demir, Mustafa Muammer; 03.10. Department of Mechanical Engineering; 03.09. Department of Materials Science and Engineering; 03. Faculty of Engineering; 01. Izmir Institute of TechnologyAn epoxy matrix filled with nonwoven mats of porous polystyrene (PS) fibers processed by an electrospinning was compression tested at quasi-static (1 × 10–3 s–1) and high strain (315 s–1) rates. The electrospun PS fibers with a diameter between 6 and 9 μm, accommodated spherical pores on the surface with the sizes ranging from 0.1 to 0.2 μm. The filling epoxy matrix with 0.2 wt % PS fibers increased the compressive elastic modulus and compressive strength over those of neat epoxy resin. The microscopic observations indicated that the surface pores facilitated the resin intrusions into the fiber, enhancing the interlocking between resin and fibers, and increased the deformation energy expenditure of the polymer matrix.