Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 1
    Citation - Scopus: 1
    Inhibition 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, Ekrem
    This 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: 6
    Citation - Scopus: 8
    Effect of the Combination of Organic Acid Solutions on Tinplate Corrosion
    (Elsevier, 2022) Yıldırım, Koray; Kızılkaya, Ali Can
    Tinplate corrosion as a result of canned food is typically tested in industry by tinplate in synthetic media based on single organic acids. However, the combination of organic acids, which is present in applied conditions, is not previously investigated in terms of its effect on tinplate corrosion mechanism. In this manuscript, we combine structural characterization of tinplate surfaces with electrochemical measurements, to investigate the corrosion mechanism of tinplate under acetic acid-NaCl, citric acid-NaCl, and a combined acetic acid, citric acid and NaCl media. The results show that the combined acid media causes does not result in a pronounced formation of a protective passivation layer, in contrast to the single acid based media. Our findings demonstrate the combined effects of the organic acids in corrosive media has to be taken into account for tinplate corrosion, as they can alter the corrosion mechanism. Furthermore, we show that combination of organic acids can accelerate tinplate corrosion testing in packaging industry. Thus, our findings can contribute to the design of new aging media for tinplate corrosion testing.
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    Polymer-Bonded Cdte Quantum Dot-Nitroxide Radical Nanoprobes for Fluorescent Sensors
    (Springer, 2022) Karabıyık, Merve; Ebil, Özgenç
    A novel functional polymer-bonded quantum dots (QDs)-nitroxide radical complex was demonstrated. In the first part of the study, the synthesis of polymer thin films via initiated chemical vapor deposition (iCVD), functionalization of polymer thin films with amine functional groups, and attachment of QDs to polymer surface were demonstrated. Fourier transform infrared spectroscopy and energy-dispersive X-ray spectroscopy together with fluorescence spectroscopy studies revealed that aliphatic primary amine (propylamine) was very effective for the functionalization of iCVD deposited poly(glycidyl methacrylate) (pGMA) and its copolymer with diethylaminoethyl methacrylate (p(GMA-co-DEAEMA)) and also QD attachment to functionalized polymer surface. In the second part of the study, the synthesis and attachment of Quantum Dot-4Amino TEMPO (QD-4AT) nanoprobes to functionalized pGMA thin films and feasibility of using them as fluorescent sensor structures were investigated. It was found that high initial 4AT concentration and long (24 h) interaction times are beneficial for nanoprobe synthesis. Electron paramagnetic resonance (EPR) spectroscopy analysis revealed the existence of covalent bond between QD and 4AT when 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide was used during synthesis. EPR analysis together with fluorescence microscopy investigation confirmed the successful attachment of nanoprobes to polymer surface. Time-depended fluorescence quenching analysis revealed that more than 50% reduction in fluorescence intensity within 15 min demonstrating the potential of polymer bonded QD-4AT nanoprobes in various sensor applications.
  • Article
    Citation - WoS: 12
    Citation - Scopus: 12
    Supercritical Fluid Reactive Deposition: a Process Intensification Technique for Synthesis of Nanostructured Materials
    (Elsevier, 2022) Yousefzadeh, Hamed; Akgün, Işık Sena; Barım, Şansım Bengisu; Sarı, Tarık Bercan; Eriş, Gamze; Uzunlar, Erdal; Bozbağ, Selmi Erim; Erkey, Can
    Supercritical fluid reactive deposition (SFRD) is a promising process intensification technique for synthesis of a wide variety of nanostructured materials. The enhanced mass transfer characteristics of supercritical fluids (SCFs) coupled with high solubilities of reducing gases in SCFs provide many advantages related to equipment size and time minimization over conventional techniques. Among SCFs, the emphasis has been placed on supercritical CO2 (scCO2) which is non-toxic, cheap and leaves no residue on the treated medium. Moreover, in SFRD, multiple processes such as dissolution, adsorption, reaction, and purification are combined in a single piece of equipment which is an excellent example of process integration for process intensification. In this review, the fundamental thermodynamic and kinetic aspects of the technology are described in detail. The studies in the literature on synthesis of a wide variety of nanostructured materials including supported nanoparticles, films, and ion-exchanged zeolites by SFRD are reviewed and summarized. The applications of these materials as catalysts and sensors are described. The review hopes to lead to further studies on further development of this technology for a wide variety of applications.
  • Article
    Citation - WoS: 21
    Citation - Scopus: 21
    A 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, Dmitri
    Pt/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: 13
    Citation - Scopus: 11
    Valorization of Olive Tree Pruning Waste for Potential Utilization in Lithium Recovery From Aqueous Solutions
    (Springer, 2022) Nampeera, Jackline; Recepoğlu, Yaşar Kemal; Yüksel, Aslı
    Olive 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: 6
    Citation - Scopus: 6
    Mathematical 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, Han
    A 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: 8
    Citation - Scopus: 11
    The Effect of Protein Bsa on the Stability of Lipophilic Drug (docetaxel)-Loaded Polymeric Micelles
    (Elsevier, 2021) Polat, Hürriyet; Çevik Eren, Merve; Polat, Mehmet
    Polymeric 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.