WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7150
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Article Citation - WoS: 27Citation - Scopus: 31Fluoroacrylate-Aromatic Acrylate Copolymers for Viscosity Enhancement of Carbon Dioxide(Elsevier Ltd., 2019) Kılıç, Sevgi; Enick, Robert M.; Beckman, Eric J.The effect of the structure of aromatic acrylate-fluoroacrylate copolymers on CO2 viscosity at elevated pressures was investigated. These copolymers were all found to be miscible with CO2 at pressures between 10-15 MPa (295 K) and induce an increase in the viscosity to some degree. It appears that stacking of aromatic rings is the key factor in viscosity enhancement. The results showed that viscosity of the solution increases with the increasing content of the aromatic acrylate unit in the copolymer, but a point is reached beyond which additional comonomer causes the relative viscosity to drop, suggesting that the aromatic rings associate through intramolecular rather than intermolecular interactions beyond the optimum value. The most effective CO2 thickener identified in this study was the 29% phenyl acrylate-71% fluoroacrylate copolymer. However, the presence of a spacer (methyl or ethyl) between the backbone and the aromatic group substantially diminished the viscosity enhancement.Article Citation - WoS: 23Citation - Scopus: 31Nano-Caco3 Synthesis by Jet Flow(Elsevier Ltd., 2017) Ülkeryıldız, Eda; Kılıç, Sevgi; Özdemir, EkremA new methodology was introduced to produce hollow nano calcite particles in homogenous size distribution without aggregation. The design consisted of a jet flow system in which the crystallization region was separated from the stabilization region. The newly produced nano CaCO3 particles of about 140 nm were removed from the crystallization region as quickly as possible into the stabilization region before aggregation or crystal growth. In the stages of crystallization, the particles started to dissolve from their edges which opened-up the pores inside the particles. At the late stages of crystallization, the open pores closed. These particles were stable in Ca(OH)2 solution and no aggregation was detected. Different particles with different morphologies can be produced by adjusting the stages in the crystallization.Article Citation - WoS: 48Citation - Scopus: 52Stability of Caco3 in Ca(oh)2 Solution(Elsevier Ltd., 2016) Kılıç, Sevgi; Toprak, Görkem; Özdemir, EkremThe effect of calcium hydroxide (Ca(OH)2) on the stability of calcium carbonate (CaCO3) particles was investigated with respect to the surface potential and particle size. Both CaCO3 and Ca(OH)2 were dissolved in ultrapure water at concentrations up to 100 mM. The solubility limits were about 18 mM for Ca(OH)2 and about 0.13 mM for CaCO3 at 23 °C in water. Dissolution of commercial CaCO3 in 10 mM of Ca(OH)2 solution and dissolution of Ca(OH)2 in 10 mM of CaCO3 slurry were also studied at similar conditions. Conductivity, pH, zeta potential, and average particle sizes were measured for each solution. The morphological characteristics of the particles were analyzed by the SEM images. It was found that the zeta potential of CaCO3 particles was greater than + 30 mV when they were placed in the Ca(OH)2 solution compared to a zeta potential value of - 10 mV in water. It was concluded that the Ca(OH)2 solution is a stabilizer for the CaCO3 particles.Article Citation - WoS: 20Citation - Scopus: 23Rice-Like Hollow Nano-Caco3 Synthesis(Elsevier Ltd., 2016) Ülkeryıldız, Eda; Kılıç, Sevgi; Özdemir, EkremWe have shown that Ca(OH)2 solution is a natural stabilizer for CaCO3 particles. We designed a CO2 bubbling crystallization reactor to produce nano-CaCO3 particles in homogenous size distribution without aggregation. In the experimental set-up, the crystallization region was separated from the stabilization region. The produced nanoparticles were removed from the crystallization region into the stabilization region before aggregation or crystal growth. It was shown that rice-like hollow nano-CaCO3 particles in about 250 nm in size were produced with almost monodispersed size distribution. The particles started to dissolve through their edges as CO2 bubbles were injected, which opened-up the pores inside the particles. At the late stages of crystallization, the open pores were closed as a result of dissolution-recrystallization of the newly synthesized CaCO3 particles. These particles were stable in Ca(OH)2 solution and no aggregation was detected. The present methodology can be used in drug encapsulation into inorganic CaCO3 particles for cancer treatment with some modifications.Article Citation - WoS: 14Citation - Scopus: 15Effect of Carbonic Anhydrase on Caco3 Crystallization in Alkaline Solution(American Chemical Society, 2016) Molva, Murat; Kılıç, Sevgi; Özdemir, EkremThe effect of bovine carbonic anhydrase (CA) on calcium carbonate (CaCO3) crystallization was investigated. A new method was developed to estimate the biocatalytic activity of CA in alkaline solution. The CA was immobilized within polyurethane (PU) foam, and compared its biocatalytic activity with the free-CA and bare-PU foam. A minireactor was created in a calcium hydroxide (Ca(OH)2) solution in order to control the CO2 transfer rate, and reproducible results were obtained. It was found that the free-CA lost its activity in less than 6 min at pH 12.5 in alkaline Ca(OH)2 solution. The CaCO3 crystallization rates for the immobilized-CA were found to be a U-shape, relatively lower at lower immobilized-CA amounts compared to those for the free-CA and bare-PU foam and higher when the amount of immobilized-CA increased. It was concluded that a higher immobilized-CA amount is required to accelerate the CaCO3 crystallization rates in Ca(OH)2 solution.Article Citation - WoS: 40Citation - Scopus: 46Influence of Tert-Amine Groups on the Solubility of Polymers in Co2(Elsevier Ltd., 2009) Kılıç, Sevgi; Wang, Yang; Johnson, J. Karl; Beckman, Eric J.; Enick, Robert M.There is a need to develop new, non-fluorous polymers that are highly soluble in CO2. Experimental evidence indicates that tertiary amine and pyridine groups may exhibit favorable Lewis acid-Lewis base type interactions with CO2. It is therefore reasonable to assume that incorporation of tertiary amines into the side chain or backbone of non-fluorous polymers may impart a degree of CO2-solubility to the polymer. We present experimental results for eight different tert-amine-containing polymers. Of these polymers, only propyl dimethylamine-functionalized poly(dimethylsiloxane) is soluble in CO2 at temperatures and pressures accessible in our experiments, but even this polymer is less soluble than non-functionalized poly(dimethylsiloxane) at the same chain length. We have performed ab initio calculations on tertiary amine-containing moieties representative of some of the polymers examined experimentally. Our calculations confirm that amine-CO2 interactions are indeed energetically favorable. However, we also find that the moiety self-interactions are typically more favorable than the CO2-moiety interactions. This indicates that the lack of solubility of amine-containing polymers in CO2 is a direct result of strong polymer-polymer interactions.