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: 9Citation - Scopus: 9Hollow Nano-caco3's Voc Sensing Properties: a Dft Calculation and Experimental Assessments(Elsevier, 2023) Bayram, Abdullah; Farzaneh, Amir; Esrafili, Mehdi D.; Okur, Salih; Özdemir, EkremAir is the most critical and necessary for life, and air quality significantly impacts people's health. Both indoor and outdoor pollution frequently contain volatile organic compounds (VOCs). Such contaminants provide immediate or long-term health risks to the living system. The present study investigates sorption characteristics of VOCs on hollow nano calcite (CaCO3) particles with 250 nm and 40 nm pore sizes to remove from the air ambient using the quartz crystal microbalance (QCM) technique at room temperature both experimentally and theoretically. The results were supported by density functional theory (DFT), and adsorption-desorption characteristics were studied with Langmuir adsorption isotherms. The QCM measurements showed a stable signal without having hysteresis, and the response of polar VOCs on hollow nano-CaCO3 particles such as ethanol, propanol, and humidity with higher polarity was less compared to solvents such as chloroform and dichloromethane, which revealed that the surfaces of CaCO3 particles have mostly non-polar properties. CaCO3 surface and VOC molecule interactions overlap with the Langmuir model. With DFT calculations, VOC and water molecule adsorption changes the CaCO3 Egap. Our findings show that the ΔEgap values increase as chloroform > dichloromethane > propanol > ethanol > water. This order suggests that the sensing response of the hollow CaCO3 structure is linearly proportional to the adsorption energies of VOC and water. The linear adsorption characteristics, high sensing response, and short recovery time illustrated that the newly synthesized nano-CaCO3 could be implemented as a new VOC adsorbent material for health, environmental sustainability, and in vitro microbiome cultures.Article Citation - WoS: 21Citation - Scopus: 22Role of Ph on Co2 Sequestration in Coal Seams(Elsevier Ltd., 2016) Özdemir, EkremThe effect of acidic or basic pre-treatment on the adsorption capacity of CO2 on coals was investigated. Argonne Premium Pocahontas No. 3, Upper Freeport, Pittsburgh No. 8, Lewiston-Stockton, Blind Canyon, Illinois No. 6, Wyodak, and Beulah-Zap coals were washed in weak solutions of H2SO4 and NaOH to the pH values of 10, 7, and 2, after an initial washing in acidic water. Attempts to treat the Wyodak and Beulah-Zap coals were unsuccessful because the base treatment after the initial acid treatment resulted in a suspension which could be separated neither via filtration through a 45 μm filter nor centrifugation. Equilibration took several days in some cases, although the as-received coal had been ground to 150 μm. Acid washing preferentially removed Ca (calcite) and Mg. Aluminosilicate clays were not notably removed. Iron was removed in significant amounts only after base treatment, possibly after it was converted to hematite. The adsorption capacity of CO2 on the acid treated coals was higher than both the base treated and untreated coals. The difference in adsorption capacities for acid and base treated coals was related to the pore sizes and mineral matter removal from the coals, where the calculated average pore size was higher for acid treated coals than for the base treated coals. It is concluded that the pH decrease due to CO2 dissolution in cleat water is favored in coal seam sequestration, which resulted in an increase in storage capacity of coals.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: 70Citation - Scopus: 80Modeling of Coal Bed Methane (cbm) Production and Co2 Sequestration in Coal Seams(Elsevier Ltd., 2009) Özdemir, EkremA mathematical model was developed to predict the coal bed methane (CBM) production and carbon dioxide (CO2) sequestration in a coal seam accounting for the coal seam properties. The model predictions showed that, for a CBM production and dewatering process, the pressure could be reduced from 15.17 MPa to 1.56 MPa and the gas saturation increased up to 50% in 30 years for a 5.4 × 105 m2 of coal formation. For the CO2 sequestration process, the model prediction showed that the CO2 injection rate was first reduced and then slightly recovered over 3 to 13 years of injection, which was also evidenced by the actual in seam data. The model predictions indicated that the sweeping of the water in front of the CO2 flood in the cleat porosity could be important on the loss of injectivity. Further model predictions suggested that the injection rate of CO2 could be about 11 × 103 m3 per day; the injected CO2 would reach the production well, which was separated from the injection well by 826 m, in about 30 years. During this period, about 160 × 106 m3 of CO2 could be stored within a 21.4 × 105 m2 of coal seam with a thickness of 3 m.Article Citation - WoS: 123Citation - Scopus: 134Effect of Moisture on Adsorption Isotherms and Adsorption Capacities of Co2 on Coals(American Chemical Society, 2009) Özdemir, Ekrem; Schroeder, KarlThe effect of moisture on the adsorption isotherms and adsorption capacities of CO 2 on Argonne Premium coals has been investigated. In some experiments a small hysteresis was observed between the adsorption and desorption isotherms. The hysteresis was absent or negligible for high-rank and as-received coals but was discernible for lower rank and dried coals. An equation that accounted for the volumetric changes when an adsorbate alters the structure of an adsorbent was employed to interpret the data. The best-fit solutions indicate that the coal volume decreases upon drying. The microscopic shrinkage estimated using helium expansion was greater than the shrinkage reported using the bed-height technique. The microscopic shrinkage was 5-10% for low-moisture medium and high-rank coals and up to 40% for low-rank coals having higher moisture contents. The CO 2 swelling of coals during adsorption isotherm measurements was estimated to be about the same as the shrinkage that occurred during the moisture loss. The adsorption capacity, isosteric heat of adsorption, average pore size, and surface area of the as-received (moist) and dried Argonne coals were estimated after accounting for the volume changes. The isosteric heat of adsorption of CO 2 was found to be between 23 and 25 kJ/mol for as-received coals and between 25 and 27 kJ/mol for dried coals, regardless of the rank. The degree of drying was shown to affect the adsorption capacity and the calculated surface area. For dried coals, the adsorption capacity showed the typical 'U-shape' dependence on rank whereas the as-received coals displayed a more linear dependence. A relationship is proposed to quantify the effect of moisture on the adsorption capacity. The mechanism of CO 2 adsorption on moist coals and the implications of the lower adsorption capacity of wet coals to coal seam sequestration of CO 2 are presented.Article Citation - WoS: 88Citation - Scopus: 108Biomimetic Co2 Sequestration: 1. Immobilization of Carbonic Anhydrase Within Polyurethane Foam(American Chemical Society, 2009) Özdemir, EkremBovine carbonic anhydrase (CA) was immobilized within polyurethane (PU) foam for biomimetic CO2 sequestration. The catalytic activities for the free and immobilized CA were estimated using paranitrophenyl acetate (p-NPA) as the substrate. Because the p-NPA has limited solubility in the aqueous phase, the activities were estimated in Tris buffer containing 10% acetonitrile. A Lineweaver-Burk relationship was employed to estimate the Michaelis-Menten kinetic parameters for the free and immobilized CA. The kcat, K m, and kcat/Km values for the free CA were found to be 2.02 s-1, 12.2 mM, and 166.4M-1 s-1, respectively. The Km value for the immobilized CA was estimated to be 9.6mMat the same conditions. The immobilized CA was stable and did not lose any activity over seven consecutive washings and activity tests. While the free CA lost its activity in 45 days stored at 4 °C in refrigerator, the immobilized CA maintained 100% of its activity over a 45 day period stored in Tris buffer at ambient conditions. It was concluded that the immobilized CA as a very stable biocatalyst could be employed in biomimetic CO2 sequestration.
