Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Jelatin Doku İskelesinin Mekanik Özellikleri Üzerine Gözenek Oluşturucu Ajanın Boyutu ve Bağlantı Süresinin Etkileri(Manisa Celâl Bayar Üniversitesi, 2015) Büyüköz, Melda; Alsoy Altınkaya, SacideBu çalışmada, makrogözenekli ve gözenekleri birbirleri ile bağlantılı olarak kalıplama, ısı etkili faz ayrımı ve tanecik uzaklaştırma yöntemleri ile üretilen jelatin bazlı doku iskelelerinde gözenek oluşturucu ajan olan parafin kürelerin boyutu ve bağlantı sürelerinin doku iskelelerinin mekanik özellikleri üzerine olan etkileri incelenmiştir. Sünger formlu ve açık hücreli yapıda olan doku iskelelerinin mekanik özellikleri sıkıştırma testi ile ölçülmüştür. Yapılan ölçümler parafin küre çapındaki artışın doku iskelelerinin sıkıştırma katsayısını istatistiksel olarak anlamlı bir şekilde etkilemediğini göstermiştir. Ancak, parafin kürelerin maruz bırakıldığı ısı etkileşim süresinin 100 dakikadan 400 dakikaya arttırılmasının 250-425 µm çapındaki parafin kürelerle hazırlanan doku iskelesinin elastisite değerini arttırdığı belirlenmiştir (p<0.05). Ayrıca, 425-600 µm çapındaki parafin kürelerle hazırlanan doku iskelelerinde, ısı etkileşim süresi 100 dakikadan 400 dakikaya arttırıldığında sıkıştırma katsayısı anlamlı bir şekilde azalmıştır (p<0.05). Elde edilen sonuçlar, bu tür doku iskelelerinde parafin kürelerin boyutundan çok bağlantı süresinin mekanik özellikler üzerinde etkili olduğunu göstermiştirConference Object Predicting Drying in Solvent-Coated Polymeric Films(American Chemical Society, 2000) Alsoy Altınkaya, Sacide; Duda, John Larry[No abstract available]Conference Object Development of Functional Materials for Sirna Delivery and Neural Tissue Engineering(AIChE, 2015) Uz, Metin; Alsoy Altınkaya, Sacide; Mallapragada, Surya K.The current nonviral siRNA delivery systems in the literature face many problems such as, cellular entry, endosomal escape and efficient siRNA release. Considering this motive, we developed gold nanoparticles (AuNPs) and temperature/pH responsive pentablock copolymer based siRNA delivery systems to address these problems. The temperature and pH responsive cationic and amphiphilic pentablock copolymers, which were consisted of the temperature responsive Pluronic F127 middle block constructed by PEO-PPO-PEO ((poly(ethyleneoxide)-block-poly(propyleneoxide)-block-poly(ethyleneoxide))) blocks contributing cellular entry through temperature responsive micellization and pH responsive cationic PDEAEM (poly(2-diethylaminoethyl methacrylate)) end blocks facilitating nucleic acid condensation and endosomal escape, were used for the first time in the development of polyplex and AuNP based multicomponent siRNA delivery systems (MCSs). The results indicated that systems managed to protect siRNA from external effects, maintain the system stability, facilitate cellular entry and enhance endosomal escape. It was noted that the transfection efficiency of the MCSs, which were boosted by the presence of cleavable disulfide bond, was ~15% higher than the commercial product RNAiMax while the efficacy of polyplexes alone were similar to the RNAiMax.Book Citation - Scopus: 5Editors’ Foreword(CRC Press, 2017) Figoli, A.; Hoinkis, Jan; Altinkaya, Sacide Alsoy; Bundschuh, JochenThe book focuses on Application of Nanotechnology in Membranes for Water Treatment but not only provides a series of innovative solutions for water reclamation through advanced membrane technology but also serves as a medium to promote international cooperation and networking for the development of advanced membrane technology for Universal well-being and to achieve the common goal of supplying economically, environmentally and societally sustainable freshwater and better sanitation systems. This book is unique because the chapters were authored by established researchers all around the globe based on their recent research findings. In addition, this book provides a holistic coverage of membrane development for water treatment, from the membrane preparation and characterizations to the performance for specific processes and applications. Since that water scarcity has become a global risk and one of the most serious challenges for the scientific community in this century, the publication of this book is therefore significant as it will serve as a medium for a good reference of an alternative solution in water reclamation. This book will provide the readers with a thorough understanding of the different available approaches for manufacturing membranes both with innovative polymeric systems and inorganic nano-materials which could give enhanced functionalities, catalytic and antimicrobial activities to improve the performance of the existing membranes. It will be useful for leading decision and policy makers, water sector representatives and administrators, policy makers from the governments, business leaders, business houses in water treatment, and engineers/ scientists from both industrialized and developing countries as well. © 2019 Elsevier B.V., All rights reserved.Article Citation - WoS: 28Citation - Scopus: 29Development of a High-Flux Thin-Film Composite Nanofiltration Membrane With Sub-Nanometer Selectivity Using a Ph and Temperature-Responsive Pentablock Co-Polymer(American Chemical Society, 2019) Bar, Canbike; Çağlar, Nagahan; Uz, Metin; Mallapragada, Surya K.; Alsoy Altınkaya, SacideProducing block co-polymer-based nanofiltration (NF) membranes with sharp molecular weight cutoffs via an efficient method exhibiting persistent size-based separation quality is challenging. In this study, this challenge was addressed by reporting a facile approach to fabricate pentablock co-polymer (PBC)-based thin-film composite (TFC) NF membranes. The PBC, consisting of temperature-responsive Pluronic F127 (PEO-b-PPO-b-PEO) middle blocks and pH-responsive poly(N,N-(diethylamino)ethyl methacrylate) end blocks, were synthesized by atom-transfer radical polymerization. This polymer was then attached electrostatically to the surface of polysulfone/sulfonated polyether-sulfone support membranes fabricated using a non-solvent-induced phase separation technique. The conformational changes of the PBC chains in response to pH and temperature determined the, pure water flux and neutral solute (PEG 1000) rejection performance of TFC membranes. Permeability of the membranes increased from 13.0 +/- 0.63 to 15.9 +/- 0.06 L/m(2).h bar and from 6.7 +/- 0.00 to 13.9 +/- 0.07 L/m(2).h.bar by changing the solution pH from 4 to 8.5 and temperature from 4 to 25 degrees C, respectively. The pH- and temperature-responsive conformational changes did not affect the PEG 1000 rejection and membrane pore radius, which remained constant at similar to 89% and similar to 0.9 nm, respectively. This important finding was attributed to the high grafting density of co-polymer chains, resulting in spatial limitations among the grafted chains. The pore size of similar to 0.9 nm achieved with the proposed membrane design is the smallest size reported so far for membranes fabricated from block copolymers. TFC membranes demonstrated high stability and maintained their flux and rejection values under both static (storage in an acidic solution for up to 1 month) and dynamic (filtering PEG 1000 solution over 1 week) conditions. Pentablock copolymers enable a NF membrane with a sharp molecular weight cutoff suitable for size-selective separations. The membrane fabrication technique proposed in this study is a scalable and promising alternative that does not involve complex synthetic routes.Article Citation - WoS: 30Citation - Scopus: 44A Review on Computational Modeling Tools for Mof-Based Mixed Matrix Membranes(MDPI Multidisciplinary Digital Publishing Institute, 2019) Keskin, Seda; Alsoy Altınkaya, SacideComputational modeling of membrane materials is a rapidly growing field to investigate the properties of membrane materials beyond the limits of experimental techniques and to complement the experimental membrane studies by providing insights at the atomic-level. In this study, we first reviewed the fundamental approaches employed to describe the gas permeability/selectivity trade-off of polymer membranes and then addressed the great promise of mixed matrix membranes (MMMs) to overcome this trade-off. We then reviewed the current approaches for predicting the gas permeation through MMMs and specifically focused on MMMs composed of metal organic frameworks (MOFs). Computational tools such as atomically-detailed molecular simulations that can predict the gas separation performances of MOF-based MMMs prior to experimental investigation have been reviewed and the new computational methods that can provide information about the compatibility between the MOF and the polymer of the MMM have been discussed. We finally addressed the opportunities and challenges of using computational studies to analyze the barriers that must be overcome to advance the application of MOF-based membranes.Article Citation - WoS: 34Citation - Scopus: 35Development of High Flux Nanofiltration Membranes Through Single Bilayer Polyethyleneimine/Alginate Deposition(Elsevier Ltd., 2019) Tekinalp, Önder; Alsoy Altınkaya, SacideThe aim of this study is to prepare high flux, stable, antifouling nanofiltration membranes through single bilayer polyelectrolyte deposition. To this end, a tight ultrafiltration support membrane was prepared from a polysulfone/sulfonated polyethersulfone blend. Deposition of a polyethyleneimine and alginate pair on this support has reduced the molecular weight cut off from 6 kDa to below 1 kDa. The pure water permeability and polyethylene glycol 1000 rejection of the coated membrane were found to be 15.5 ± 0.3 L/m2·h·bar and 90 ± 0.6%, respectively, by setting the deposition pH for each layer to 8 and the ionic strengths to 0.5 M and 0 M. This membrane has exhibited significantly higher permeability than commercial membranes with the same molecular weight cut off, retaining 98% of the initial flux during 15 h filtration of bovine serum albumine. In addition, the membrane has been able to completely remove anionic dyes from aqueous solution by showing 99.9% retentions to Reactive red 141, Brilliant blue G and Congo red with a 2 bar transmembrane pressure. High flux and membrane stability in acidic and salty environments have been achieved when deposition conditions favor high adsorption levels for the first layer and strong ionic cross-linking between the carboxyl group on the alginate and the amine groups on the polyethyleneimineArticle Citation - WoS: 49Citation - Scopus: 55A Facile Approach for Preparation of Positively Charged Nanofiltration Membranes by In-Situ Crosslinking Between Polyamide-Imide and Polyethylenimine(Elsevier Ltd., 2018) Cihanoğlu, Aydın; Alsoy Altınkaya, SacidePolyamide-imides (PAI) are attractive materials for membrane formation due to their high chemical and thermal stability. In this study, we report a facile approach for preparing positively charged nanofiltration (NF) membranes using a one-step process. Polyethylenimine (PEI) was dissolved in a coagulation bath and formed in-situ ionic crosslinking with PAI during phase inversion. The membranes were characterized by attenuated total reflectance Fourier Transform Infrared spectroscopy (ATR-FTIR), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), atomic force microscopy (AFM), contact angle and zeta potential measurements. The most positively charged membrane was obtained when the pH of the coagulation bath was adjusted to 10. This membrane showed a significant decrease in contact angle and surface roughness and increase in the pure water permeability (PWP) compared to the plain PAI membrane. The salt rejection performance of the crosslinked PAI membrane was measured using MgCl2, CaCl2, NaCl and Na2SO4 salts. The rejection of Mg2+ and Ca2+ ions was found to be 95.6% and 90.2%, respectively. The crosslinked membrane showed excellent chemical stability when stored in HCl solution at pH 3 up to 7 days. Antifouling behaviour of the optimized membrane was tested using bovine serum albumin (BSA) and flux recovery ratio of the membrane was found to be 92.2% at the end of 3 h filtration. The results suggest that the positively charged PAI membranes crosslinked with PEI may have a potential in recovering valuable cationic metals from acid mine wastewater.Article Citation - WoS: 1Citation - Scopus: 1The Effect of Mass Transfer Resistance and Nonuniform Initial Solvent Concentration on Permeation Through Polymer Membranes(John Wiley and Sons Inc., 2018) Zielinski, John M.; Alsoy Altınkaya, SacideA numerical simulation model has been developed which enables one to examine the effects of surface mass transfer resistance on the evaluation of permeation (P*), diffusion (D), and solubility (S) coefficients from unsteady-state mass transfer experiments as well as the transmission rate. A complementary analytical expression has been developed which validates the numerical model and facilitates the evaluation of the concentration dependence of P*, D, and S from sequential step-change experiments, under experimental conditions when the surface mass transfer resistance can be neglected.Article Citation - WoS: 27Citation - Scopus: 37Nanofibrous Gelatine Scaffolds Integrated With Nerve Growth Factor-Loaded Alginate Microspheres for Brain Tissue Engineering(John Wiley and Sons Inc., 2018) Büyüköz, Melda; Erdal, Esra; Alsoy Altınkaya, SacideNeural regeneration research is designed in part to develop strategies for therapy after nerve damage due to injury or disease. In this study, a new gelatine-based biomimetic scaffold was fabricated for brain tissue engineering applications. A technique combining thermally induced phase separation and porogen leaching was used to create interconnected macropores and nanofibrous structure. To promote tissue regeneration processes, the scaffolds were integrated with nerve growth factor (NGF)-loaded alginate microspheres. The results showed that nanofibrous matrix could only be obtained when gelatine concentration was at least 7.5% (w/v). The scaffold with a modulus value (1.2 kPa) similar to that of brain tissue (0.5–1 kPa) was obtained by optimizing the heat treatment time, macropore size and gelatine concentration. The encapsulation efficiencies of NGF into 0.1% and 1% alginate microspheres were 85% and 100%, respectively. The release rate of NGF from the microspheres was controlled by the alginate concentration and the poly(L-lysine) coating. The immobilization of the microspheres in the scaffold reduced burst release and significantly extended the release period. The nanofibrous architecture and controlled release of NGF from the microspheres induced neurite extension of PC12 cells, demonstrating that the released NGF was in an active form. The results suggest that the scaffolds prepared in this study may have potential applications in brain tissue engineering due to topologic and mechanical properties similar to brain tissue and pore structure suitable for cell growth and differentiation.