Chemical Engineering / Kimya Mühendisliği
Permanent URI for this collectionhttps://hdl.handle.net/11147/14
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Article Citation - WoS: 1Citation - Scopus: 1Inhibition of Caco3 Growth and Synthesis of Submicron Particles by Preferential Adsorption of Additive Ca2+ Ions on Fresh Precipitates(Royal Society of Chemistry, 2022) Majekodunmi, Olukayode T.; Kılıç Özdemir, Sevgi; Özdemir, EkremThis study demonstrates a method to inhibit the growth of CaCO3 and synthesize submicron particles in a chemical precipitation process under ambient and high supersaturation conditions. Equimolar CaCl2 and Na2CO3 solutions were mixed in a model tubular reactor at a constant flow rate, and the precipitates were continuously dispersed in stirred 250 mL of 10 mM Ca(OH)2 solution. This approach resulted in the synthesis of colloidally stable submicron CaCO3 particles for a precipitant concentration ≤75 mM. Varying the precipitates’ retention time in the tubular reactor had no significant effects on the particle size and colloidal stability. Time-dependent changes in the mean size, crystal form, morphology and specific surface area of the synthesized particles were also studied. For a precipitant concentration of 75 mM, the particles were monodispersed and porous spindle-like scalenohedral crystals which gradually grew in all faces as more precipitates were fed into the Ca(OH)2 solution. The mean hydrodynamic size of the particles was ∼850 nm at the 8th minute. However, in the absence of additive Ca2+ ions, the particles obtained at the 8th minute were polydisperse mixtures of vaterite and rhombohedral calcite particles greater than 4 μm in size. The results show that free additive Ca2+ ions are irreversibly adsorbed onto the particles as the precipitates dissolve and recrystallize into smaller crystals upon reaching the Ca(OH)2 solution.Article Citation - WoS: 3Citation - Scopus: 4Microfluidic-Assisted Preparation of Nano and Microscale Chitosan Based 3d Composite Materials: Comparison With Conventional Methods(Wiley, 2022) Kimna, Ceren; Değer, Sibel; Tamburacı, Sedef; Tıhmınlıoğlu, FundaAlthough nanofillers contribute to improved physical characteristics and biological functionalities of polymer-based biomaterials, their dispersion in polymer matrices is still a challenging issue in terms of obtaining consistency for the inherent properties. To tackle this problem, homogenization techniques are applied to disperse the nanofillers in such polymers, however, these methods can cause undesired changes especially in the rheological properties and the physical structure of the biopolymer matrices. Recently, as a novel homogenization technique, microfluidization has been used to homogenize polymer nanocomposites to minimize these limitations. In this study, two different nanocomposite structures as chitosan/montmorillonite (CS/MMT) and chitosan/polyhedral oligomeric silsesquioxane nanocages (CS/POSS) were homogenized with microfluidization and investigated in terms of physical alterations. Furthermore, the effect of microfluidizer technique on material characteristics was compared with conventional homogenization techniques, i.e., ultrasonic bath and sonication in terms of solution, nano – (e.g., hydrodynamic size, drug encapsulation) and macroscopic material characteristics (e.g., porosity, mechanical properties, swelling and thermal degradation). It was found that the microfluidizer homogenization improves the physical characteristics in both nano and macroscale materials: Nanospheres obtained from CS/MMT composites showed enhanced stability, uniform size distribution (<100 nm, PDI: [removed]50%) whereas 3D porous CS/POSS scaffolds showed improved structural uniformity (i.e., homogeneous and interconnected microstructure) and enhanced thermal and mechanical properties. The obtained results indicate that the microfluidizer homogenization ensures a successful nanofiller dispersion in polymer matrices, thereby improving the biomaterial characteristics impressively compared to the sonication methods.Article Citation - WoS: 21Citation - Scopus: 21A Promising Catalyst for the Dehydrogenation of Perhydro-Dibenzyltoluene: Pt/Al2 O3 Prepared by Supercritical Co2 Deposition(MDPI, 2022) Modisha, Phillimon; Garidzirai, Rudaviro; Güneş, Hande; Bozbağ, Selmi Erim; Rommel, Sarshad; Uzunlar, Erdal; Aindow, Mark; Erkey, Can; Bessarabov, DmitriPt/Al2 O3 catalysts prepared via supercritical deposition (SCD), with supercritical CO2, wet impregnation (WI) methods and a selected benchmark catalyst, were evaluated for the dehydrogenation of perhydro-dibenzyltoluene (H18-DBT) at 300◦ C in a batch reactor. After ten dehydrogenation runs, the average performance of the catalyst prepared using SCD was the highest compared to the benchmark and WI-prepared catalysts. The pre-treatment of the catalysts with the product (dibenzyltoluene) indicated that the deactivation observed is mainly due to the adsorbed H0-DBT blocking the active sites for the reactant (H18-DBT). Furthermore, the SCD method afforded a catalyst with a higher dispersion of smaller sized Pt particles, thus improving catalytic performance towards the dehydrogenation of H18-DBT. The particle diameters of the SCD-and WI-prepared catalysts varied in the ranges of 0.6–2.2 nm and 0.8–3.4 nm and had average particle sizes of 1.1 nm and 1.7 nm, respectively. Energy dispersive X-ray spectroscopy analysis of the catalysts after ten dehydrogenation runs revealed the presence of carbon. In this study, improved catalyst performance led to the production of more liquid-based by-products and carbon material compared to catalysts with low catalytic performance.Article Citation - WoS: 13Citation - Scopus: 11Valorization of Olive Tree Pruning Waste for Potential Utilization in Lithium Recovery From Aqueous Solutions(Springer, 2022) Nampeera, Jackline; Recepoğlu, Yaşar Kemal; Yüksel, AslıOlive tree pruning waste, mainly composed of olive branches, was converted into a value-added and sustainable product capable of lithium as a biosorbent through alkali treatment and phosphorylation reaction. Characterization studies were performed by SEM–EDX, XPS, FTIR, and TGA. Factors affecting biosorption mechanism, i.e., sorbent dosage, pH, initial Li+ concentration and temperature, and competitive ions’ presence, were investigated the synthesized functionalized olive branches (FOB). A commercial lithium selective resin, Lewatit TP 260, was also compared with FOB in batch and column studies. The Freundlich model fits adsorption isotherms better than the Langmuir model, with a maximum adsorption capacity of 6.7 mg/g at 30 °C and pH 7–8. Kinetic studies proved fast kinetics and equilibrium were attained in 6 min, while thermodynamic studies showed an exothermic (Δ Ho= - 17.52 kJ/ mol) , spontaneous reaction Δ Go< 0 at all temperatures), and increased randomness Δ So= + 24.27 J/ mol. K) at the interaction interface. Column studies revealed that although Lewatit TP 260 resin showed higher sorption capacity, its desorption efficiency (50.42%) was lower than that of FOB (99.9%), and the degree of column utilization of FOB (56.81%) was better than Lewatit TP 260 resin’s (16.0%). The findings were encouraging in the successful synthesis of a promising biosorbent from an abundant waste in Turkey for use in sustainable lithium recovery from aqueous sources. Graphical abstract: [Figure not available: see fulltext.]Article Citation - WoS: 5Citation - Scopus: 5Novel Biopolymer-Based Hydrogels Obtained Through Crosslinking of Keratose Proteins Using Tetrakis(hydroxymethyl) Phosphonium Chloride(Springer, 2022) Yalçın, Damla; Top, AybenMerino wool obtained from the Karacabey region of Turkey was solubilized using peracetic acid oxidation. The wool and extracted wool proteins (keratose) were characterized using SEM, XRD, TGA, and FTIR analyses. SDS-PAGE result of the keratose indicated diffusive bands were populated between ~ 40 and ~ 55 kDa, corresponding to low-sulfur content α-keratose proteins. Chemically crosslinked hydrogels were prepared using the keratose and tetrakis(hydroxymethyl) phosphonium chloride (THPC). Storage moduli of the hydrogels prepared at 1:1, 1:2, and 1:4 keratose to THPC reactive group ratios were measured as 63 ± 22, 291 ± 21, and 804 ± 53 Pa, respectively. Crosslinking degrees of the hydrogels also affected the secondary structures of the keratose films obtained from the drying of the hydrogels. The hydrogel with the highest crosslinking density (1:4 gel) exhibited the lowest swelling ratio, whereas the one with the lowest crosslinking density (1:1 gel) disintegrated in deionized water within less than 6 h. CCK-8 tests using L929 mouse fibroblast cells showed that all the hydrogels promoted cell proliferation. These results suggest THPC crosslinked hydrogels prepared at the millimolar THPC concentrations are biocompatible scaffolds, which can be utilized in drug delivery and tissue engineering applications. Graphical abstract: [Figure not available: see fulltext.]Article Citation - WoS: 6Citation - Scopus: 6Mathematical Modelling of the Liquid/Liquid Mass Transfer Behaviour in Gas Stirred Ladles(Taylor & Francis, 2022) Zhang, Han; Conejo, Alberto N.; Dutta, Abhishek; Ramírez-Argáez, Marco A.; Yan, HanA three-dimensional numerical model consistent with physical simulations (water/oil/thymol) has been developed to explore the mass transfer behaviour of sulphur. Euler-Lagrangian and Euler-Euler, were applied to simulate the multiphase flow; compared with experimental data, the Euler-Euler method was more accurate. The small eddy model was used for mass transfer calculations. As a new type of bottom stirring scheme, the effect of central-eccentric parallel injection on mass transfer was investigated. Moving the eccentric nozzle towards the sidewall or increasing the number of eccentric nozzles decreases the mass transfer rate at a constant total gas flow rate. The mass transfer rate increases with increasing central gas flow rate under the differential flow bottom stirring scheme. The single-nozzle central injection is still considered the most superior bottom-blowing scheme. The bubble diameter has an insignificant effect on the liquid–liquid mass transfer. The mass transfer rate of thymol is weakly accelerated with increasing bubble diameter.Article Citation - WoS: 7Citation - Scopus: 7Synthesis and Characterization of Single-Walled Carbon Nanotube: Cyto-Genotoxicity in Allium Cepa Root Tips and Molecular Docking Studies(Wiley, 2022) İnce Yardımcı, Atike; İstifli, Erman Salih; Açıkbaş, Yaser; Liman, Recep; Yağmurcukardeş, Nesli; Yılmaz, Selahattin; Ciğerci, İbrahim HakkıHerein, single-walled carbon nanotubes (SWCNTs) were synthesized by the thermal chemical vapor deposition (CVD) method, and characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), Raman spectroscopy, dynamic light scattering (DLS), and thermo-gravimetric analysis (TGA). The results indicated that obtained nanotubes were SWCNTs with high crystallinity and their average diameter was 10.15 ± 3 nm. Allium cepa ana–telophase and comet assays on the root meristem were employed to evaluate the cytotoxic and genotoxic effects of SWCNTs by examining mitotic phases, mitotic index (MI), chromosomal aberrations (CAs), and DNA damage. A. cepa root tip cells were exposed to SWCNTs at concentrations of 12.5, 25, 50, and 100 μg/ml for 4 h. Distilled water and methyl methanesulfonate (MMS, 10 μg/ml) were used as the negative and positive control groups, respectively. It was observed that MIs decreased statistically significantly for all applied doses. Besides, CAs such as chromosome laggards, disturbed anaphase–telophase, stickiness and bridges and also DNA damage increased in the presence of SWCNTs in a concentration-dependent manner. In the molecular docking study, the SWCNT were found to be a strong DNA major groove binder showing an energetically very favorable binding free energy of −21.27 kcal/mol. Furthermore, the SWCNT interacted effectively with the nucleotides on both strands of DNA primarily via hydrophobic π and electrostatic interactions. As a result, cytotoxic and genotoxic effects of SWCNTs in A. cepa root meristematic cells which is a reliable system for assessment of nanoparticle toxicology were demonstrated in this study.Article Citation - WoS: 7Citation - Scopus: 11Hydrophobic Deep Eutectic Solvent Effect on Acrylic Acid Separation From Aqueous Media by Using Reactive Extraction and Modeling With Response Surface Methodology(Taylor & Francis, 2022) Lalikoğlu, Melisa; Aşçı, Yavuz Selim; Sırma Tarım, Burcu; Yıldız, Mahmut; Arat, RefikHydrophobic deep eutectic solvents (HDES) are new-generation green solvents that have emerged in recent years. In this study, the efficiency of using HDES as a solvent in separating acrylic acid from its aqueous solution by reactive extraction method was investigated. As a solvent, HDES prepared with a mixture of TOPO and menthol has been used for the recovery of acrylic acid for the first time. Physical properties of HDES mixtures such as density, viscosity, and refractive index were determined. In reactive extraction experiments, TOPO, one of the two basic components in the solvent, was also employed as an extractant. With the help of response surface methodology based on Box-Behnken design, the effect of the parameters of amount of extractant (0.1–0.9 g), Menthol/TOPO molar ratio (2–4), and initial acid concentration (3–9%) on the distribution coefficient was investigated and the model equation was formed. The highest distribution coefficient (D = 7.8) was achieved with the molar ratio of Menthol/TOPO is 2. Upon examining all the results obtained, it was seen that more than 90% of acrylic acid could be extracted from the aqueous phase to the organic phase.Article Citation - WoS: 8Citation - Scopus: 11The Effect of Protein Bsa on the Stability of Lipophilic Drug (docetaxel)-Loaded Polymeric Micelles(Elsevier, 2021) Polat, Hürriyet; Çevik Eren, Merve; Polat, MehmetPolymeric micelles are promising delivery vehicles for improving the efficacy of anticancer drugs and reducing their side effects. However, considering the binding ability of serum albumin, the possible interaction of micelles with the native plasma components in the bloodstream raises serious questions on micellar stability. The stability of barren or drug-loaded copolymeric micelles was investigated systematically in distilled water (DW) and simulated body fluid (SBF) solutions in the presence of a model protein. The copolymer was a Pluronic® series triblock copolymer (P-123), the drug was strongly lipophilic docetaxel (DOC) and the protein was Bovine Serum Albumin (BSA). The effect of such factors as BSA and DOC concentrations and the aging of the micellar solutions was studied. Both the barren and drug-loaded micelles were quite stable in blank DW and SBF solutions for long times up to 10 days. They lost integrity and showed no inclination to re-assemble when the BSA concentration reached a critical value, which was very close to the plasma Human Serum Albumin (HSA) concentration. The presence of DOC in the micellar cores could not prevent disintegration. The results illustrate clearly that ensuring the stability of polymeric micelles in blood plasma should be an important design factor in their use as drug carriers.
