Publications by authors named "Ceyda S Uyguner-Demirel"

Refractory organic matter (RfOM) is ubiquitous in aquatic environment and plays various roles in regulating the fate, transport, toxicity, and bioavailability of chemical species, such as metals, emerging organic contaminants, and nanomaterials. RfOM is mainly represented by humic acids (HA) as the acid insoluble fraction of organic matrix. Considering the complex and multicomponent characteristic of HA, a detailed study was designed to elucidate the fate of molecular size fractions (MSFrs) of humic under solar irradiation in the presence of polyaniline (PANI)-modified TiO composites.

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Polyaniline (PANI) is a promising conducting polymer for surface modification of TiO to overcome limitations of the use of visible light and attain increased photocatalytic efficiency for the removal of organic contaminants. In this study, a series of polyaniline modified TiO (PANI-TiO) composites were prepared by using "in-situ" chemical oxidation polymerization method. The composites were systematically characterized by Fourier transform infrared spectroscopy (equipped with an attenuated total reflection accessory, FTIR-ATR), Raman spectroscopy, X-ray diffractometry (XRD), scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDAX), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectroscopy (UV-DRS), photoluminescence spectroscopy (PL), nitrogen (N) physisorption (Brunauer - Emmett - Teller surface area (S) and Barrett-Joyner-Halenda (BJH) pore size analysis), thermogravimetry-derivative thermogravimetry (TG-DTG) techniques.

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Surface modification of TiO with polyaniline (PANI) conducting polymer has been used to achieve visible light photoresponse, thereby increasing solar photocatalytic activity. In this study, photocatalytic performances of PANI-TiO composites with different mole ratios were synthesized by the in situ chemical oxidation polymerization method and tested for the degradation of a model refractory organic matter (RfOM), namely humic acid in an aqueous medium under simulated solar irradiation in a comparative manner. Adsorptive interactions under dark conditions and interactions under irradiation were investigated as contributing factors to photocatalysis.

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Natural waters contain some carbonaceous materials referred to as dissolved organic matter, which is mainly composed of humic acids (HA). Owing to its polydispersed character related to the presence of diverse molecular size fractions (< 450 kDa to even < 1 kDa), HA displays curious reactivity in natural waters and during water treatment train. In this study, a system-based stepwise approach was tracked by characterizing HA following photolysis, adsorptive interactions, and solar photocatalysis using bare TiO, sol-gel prepared TiO, and their respective Cu-doped specimens complementary to kinetic evaluation on this respect.

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Photocatalytic disinfection practices have been applied for decades and attract current interest along with the developments in synthesis of novel photocatalysts. A survey based investigation was performed for elucidation of photocatalytic treatment details as well as disinfection mechanism of microorganisms. The present work brings significant information on the utilization of second generation TiO photocatalysts for inactivation of microorganisms typically using E.

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In search of new options to achieve removal of pharmaceuticals in the environment, combined ultrasound and ozonation has become a focus of intense investigation for wastewater treatment. In this study, three pharmaceuticals were selected as model compounds for degradation experiments: diclofenac (DCF), sulfamethoxazole (SMX) and carbamazepine (CBZ). Comparison of the degradation rates for both ozonation and combined ultrasound/ozonation treatments was performed on single synthetic solutions as well as on a mixture of the selected pharmaceuticals, under different experimental conditions.

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The photocatalytic degradation of an antibiotic, vancomycin B hydrochloride (VAN-B), has been investigated in aqueous suspensions of titanium dioxide (TiO2) by monitoring the change in its concentration as well as the production of ammonia and chlorides as a function of irradiation time. The removal of 50mg L(-1) VAN-B solution yields maximum concentrations of 2.45 and 2.

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