An insight into PANI-TiO photocatalysis of refractory organic matter through molecular size fractionation.

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.

Preparation of PANI modified TiO and characterization under pre- and post- photocatalytic conditions.

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.

Photocatalytic performance of PANI modified TiO: Degradation of refractory organic matter.

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.

Effect of oxidative and non-oxidative conditions on molecular size fractionation of humic acids: TiO and Cu-doped TiO photocatalysis.

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.

Copper-doped TiO photocatalysts: application to drinking water by humic matter degradation.

The aim of this study was to determine the photocatalytic performance of copper-doped TiO (Cu-TiO) specimens on the degradation of dissolved organic matter (DOM) represented by a model humic acid (HA). TiO was synthesized by sol-gel method from an alkoxide precursor. Cu-doped TiO specimens containing 0.

A comprehensive review on the use of second generation TiO photocatalysts: Microorganism inactivation.

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.

The role of visible light active TiO specimens on the solar photocatalytic disinfection of E. coli.

Solar photocatalytic disinfection efficiency of novel visible light activated (VLA) photocatalysts was evaluated with the aim of assessing inactivation of Escherichia coli as the pathogen indicator organism present in drinking water. Influence of humic acid (HA) on the photocatalytic disinfection efficiency of the specified VLA TiO specimens i.e.

Surface interactions of Cs and Co with bentonite.

Uptake of radioactive metal species from soils and solutions by clay particles could be a treatment option due to simplicity of operation and economic cost. In this concern, adsorption behavior of Cs or Co onto bentonite as a function of contact time, pH, initial metal concentration, ionic strength, and temperature was studied by batch adsorption technique. Adsorption isotherm data were interpreted by Langmuir, Freundlich, and Dubinin-Radushkevich (D-R) isotherm models.

Non-selective oxidation of humic acid in heterogeneous aqueous systems: a comparative investigation on the effect of clay minerals.

Application of photocatalysis for degradation of natural organic matter (NOM) has received wide interest during the last decades. Besides NOM, model compounds more specifically humic acids (HAs) were also studied. As a continuation of the previous research, TiO2 photocatalytic degradation of HA was investigated in the presence of clay minerals, i.

Oxidation of nonylphenol ethoxylates in aqueous solution by UV-C photolysis, H2O2/UV-C, Fenton and photo-Fenton processes: are these processes toxicologically safe?

UV-C, H2O2/UV-C, Fenton and photo-Fenton treatment of a nonylphenol polyethoxylate (NP-10) were comparatively studied, primarily focusing on the acute toxicity of degradation products. Formic, acetic and oxalic acids were all identified as the degradation products of NP-10; however, the sole common carboxylic acid was found to be formic acid for the studied treatment processes. The percent relative inhibition towards Vibrio fischeri increased from 9% to 33% and 24% after 120 min-UV-C and H2O2/UV-C treatment, respectively.

Advanced oxidation of a commercially important nonionic surfactant: investigation of degradation products and toxicity.

The evolution of degradation products and changes in acute toxicity during advanced oxidation of the nonionic surfactant nonylphenol decaethoxylate (NP-10) with the H2O2/UV-C and photo-Fenton processes were investigated. H2O2/UV-C and photo-Fenton processes ensured complete removal of NP-10, which was accompanied by the generation of polyethylene glycols with 3-8 ethoxy units. Formation of aldehydes and low carbon carboxylic acids was evidenced.

Photocatalytic oxidation of dinitronaphthalenes: theory and experiment.

A combination of photocatalytic oxidation experiments and quantum mechanical calculations was used in order to describe the mechanism and the nature of the photocatalytic oxidation reactions of dinitronaphthalane isomers and interprete their reactivities within the framework of the Density Functional Theory (DFT). The photocatalytic oxidation reactions of three dinitronaphthalene isomers, 1,3-dinitronaphthalene, 1,5-dinitronaphthalene and 1,8-dinitronaphthalene in the presence of TiO(2) Degussa P-25 grade were investigated experimentally. The reactions were carried out in a Solarbox photoreactor equipped with a Xenon lamp.

Photocatalytic and photoelectrocatalytic humic acid removal and selectivity of TiO(2) coated photoanode.

In this study, photocatalytic (PC) and photoelectrocatalytic (PEC) treatment methods were comparatively investigated as a possible means of removing humic acid (HA) following absorbance at 254 nm (UV(254)) and total organic carbon (TOC) analysis. The enhanced HA degradation rates were obtained in the PEC system over the conventional PC process under acidic, neutral and alkaline conditions. Preliminary and binary experiments were performed to determine the selectivity of the photoanode in terms of HA and chloride oxidation.

Application of photocatalysis as a post treatment method of a heterotrophic-autotrophic denitrification reactor effluent.

The aim of this study is the application of photocatalysis as an effective post treatment scheme for the removal of the organic matter and bacteria released by an innovative biological denitrification process referred to as heterotrophic-autotrophic denitrification, which combines heterotrophic and autotrophic denitrification processes. Photocatalytic treatment was applied using TiO2 as a photocatalyst in the loading range of 0.25-2.

Bromate formation on the non-porous TiO2 photoanode in the photoelectrocatalytic system.

The increasing use of ozone in water disinfection processes has been the focus of considerable concern in regards to inorganic disinfection by product formation of bromate in waters containing bromide. Due to the public health risk caused by the presence of bromate as a suspected carcinogen, attention had been addressed to the conditions under which bromate is formed. In this study, photoanodic bromine generation and bromate (BrO(3)(-)) formation were investigated using a TiO(2) electrode in a photoelectrocatalytic (PEC) treatment process.

Light Effects on Food.

Current research studies carried out on light-induced changes in dairy products, fats and oils, and meat products are reviewed. General factors affecting thus formed off-flavors in these food groups are the intensity of light, exposure interval, type of packaging, and some specific nutritive constituents. In dairy products, riboflavin degradation, losses of vitamin A and C are the major effects, whereas in fats and oils the effective constituents are ß-carotene, tocopherols, the undesirable flavors being related mainly to photosensitized oxidation.