Human Health Risk Assessment of the Photocatalytic Oxidation of BTEX over TiO2/Volcanic Glass.

This study demonstrates rapid photocatalytic oxidation of a benzene, toluene, ethylbenzene, and xylene (BTEX) mixture over TiO2/volcanic glass. The assessment of the photocatalytic oxidation of BTEX was conducted under conditions simulating those found in indoor environments affected by aromatic hydrocarbon release. We show, under UV-A intensities of 15 mW/cm2 and an air flow rate of 55 m3/h, that low ppmv levels of BTEX concentrations can be reduced to below detectable levels. Solid-phase microextraction technique was employed to monitor the levels of BTEX in the test chamber throughout the photocatalytic oxidation, lasting approximately 21 h. Destruction of BTEX from the gas phase was observed in the following sequence: o-xylene, ethylbenzene, toluene, and benzene. This study identified sequential degradation of BTEX, in combination with the stringent regulatory level set for benzene, resulted in the air quality hazard indexes (Total Hazard Index and Hazard Quotient) remaining relatively high during the process of photocatalytic oxidation. In the practical application of photocatalytic purification, it is crucial to account for the slower oxidation kinetics of benzene. This is of particular importance due to not only its extremely low exposure limits, but also due to the classification of benzene as a Group 1 carcinogenic compound by the International Agency for Research on Cancer (IARC). Our study underscores the importance of taking regulatory considerations into account when using photocatalytic purification technology.

Reaction Steps in Heterogeneous Photocatalytic Oxidation of Toluene in Gas Phase-A Review.

A review of the current literature shows there is no clear consensus regarding the reaction mechanisms of air-borne aromatic compounds such as toluene by photocatalytic oxidation. Potential oxidation reactions over TiO2 or TiO2-based catalysts under ultraviolet and visible (UV/VIS) illumination are most commonly considered for removal of these pollutants. Along the pathways from a model pollutant, toluene, to final mineralization products (CO2 and H2O), the formation of several intermediates via specific reactions include parallel oxidation reactions and formation of less-reactive intermediates on the TiO2 surface. The latter may occupy active adsorption sites and causes drastic catalyst deactivation in some cases. Major hazardous gas-phase intermediates are benzene and formaldehyde, classified by the International Agency for Research on Cancer (IARC) as Group 1 carcinogenic compounds. Adsorbed intermediates leading to catalyst deactivation are benzaldehyde, benzoic acid, and cresols. The three most typical pathways of toluene photocatalytic oxidation are reviewed: methyl group oxidation, aromatic ring oxidation, and aromatic ring opening.

Evaluation of dissolved and acid-leachable trace element concentrations in relation to practical water quality standards in the Syr Darya, Aral Sea Basin, South Kazakhstan.

The Syr Darya is one of the major rivers supplying the Aral Sea with freshwater. Soviet programs aimed at maximizing agricultural productivity in the Syr Darya basin increased diversion of water drastically affecting its water quality with significant consequences to its suitability for irrigation, fisheries and other uses. While water quality standards for trace elements are typically measured in the dissolved phase, there is evidence that adsorbed phases may also be relevant. Here we report potentially available heavy metals and metalloid concentrations in the Syr Darya water through the treatment of unfiltered waters samples with dilute nitric acid. Significant differences were found for most studied elements (Mann-Whitney U Test, p < 0.05) between their dissolved and acid-leachable concentrations. For Sr and Se in both sampling campaigns, no significant differences were found between their dissolved and acid-leachable concentrations, indicating their low geochemical reactivity. Dissolved V concentrations and acid-leachable Ni and Zn were found to exceed Kazakhstan Maximum Permissible Concentrations (MPC) values for the protection of fishery water quality. Our study evaluates the importance of considering regulatory issues of measuring trace metal concentrations to assess the water suitability for fisheries and irrigation.

Synthesis and Growth of Rare Earth Borates NaSrR(BO3)2 (R = Ho-Lu, Y, Sc).

NaSrR(BO3)2 (R = Ho-Lu, Y, Sc) compounds were obtained for the first time. Their structures exhibit disordered positions of Sr2+ and Na+ atoms while RO6 polyhedra are connected through the BO3 groups. Large distances between R atoms and high transparency in the range of 250-900 nm make them promising for phosphor applications. A pathway to obtain single crystals was shown by growing NaSrY(BO3)2 and NaSrYb(BO3)2 by the top seeded solution growth method with Na2O-B2O3-NaF flux.

Mn-Doped Quinary Ag-In-Ga-Zn-S Quantum Dots for Dual-Modal Imaging.

Doping of transition metals within a semiconductor quantum dot (QD) has a high impact on the optical and magnetic properties of the QD. In this study, we report the synthesis of Mn2+-doped Ag-In-Ga-Zn-S (Mn:AIGZS) QDs via thermolysis of a dithiocarbamate complex of Ag+, In3+, Ga3+, and Zn2+ and of Mn(stearate)2 in oleylamine. The influence of the Mn2+ loading on the photoluminescence (PL) and magnetic properties of the dots are investigated. Mn:AIGZS QDs exhibit a diameter of ca. 2 nm, a high PL quantum yield (up to 41.3% for a 2.5% doping in Mn2+), and robust photo- and colloidal stabilities. The optical properties of Mn:AIGZS QDs are preserved upon transfer into water using the glutathione tetramethylammonium ligand. At the same time, Mn:AIGZS QDs exhibit high relaxivity (r 1 = 0.15 mM-1 s-1 and r 2 = 0.57 mM-1 s-1 at 298 K and 2.34 T), which shows their potential applicability for bimodal PL/magnetic resonance imaging (MRI) probes.

Heterostructured g-CN/TiO2 Photocatalysts Prepared by Thermolysis of g-CN/MIL-125(Ti) Composites for Efficient Pollutant Degradation and Hydrogen Production.

Photocatalysts composed of graphitic carbon nitride (g-CN) and TiO2 were efficiently prepared by thermolysis of the MIL-125(Ti) metal organic framework deposited on g-CN. The heterojunction between the 12 nm-sized TiO2 nanoparticles and g-CN was well established and the highest photocatalytic activity was observed for the g-CN/TiO2 (3:1) material. The g-CN/TiO2 (3:1) composite exhibits high visible light performances both for the degradation of pollutants like the Orange II dye or tetracycline but also for the production of hydrogen (hydrogen evolution rate (HER) up to 1330 µmolh-1g-1 and apparent quantum yield of 0.22% using NiS as a cocatalyst). The improved visible light performances originate from the high specific surface area of the photocatalyst (86 m2g-1) and from the efficient charge carriers separation as demonstrated by photoluminescence, photocurrent measurements, and electrochemical impedance spectroscopy. The synthetic process developed in this work is based on the thermal decomposition of metal organic framework deposited on a graphitic material and holds huge promise for the preparation of porous heterostructured photocatalysts.

Synthesis of Core/Shell ZnO/rGO Nanoparticles by Calcination of ZIF-8/rGO Composites and Their Photocatalytic Activity.

A facile two-step method was developed to prepare core/shell ZnO/rGO particles from ZIF-8/rGO composites. ZIF-8 particles were first grown at the surface of rGO sheets. Next, ZIF-8 particles were transformed into ZnO particles by thermal decomposition under air at 500 °C. All materials were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Raman spectroscopy, thermogravimetric analysis, and Brunauer-Emmett-Teller analyses. Results obtained show that ZIF-8 particles strongly associate with rGO sheets and that the calcination of this material produces porous core/shell ZnO/rGO particles with an average diameter of ca. 40 nm. The wt % of rGO associated with ZIF-8 particles was varied from 5 to 20%. The ZnO/rGO (10%) particles exhibit the highest photocatalytic activity for the degradation of the Orange II dye under simulated solar light irradiation of weak intensity (5 mW/cm2). This high photocatalytic activity was demonstrated to originate from superoxide O2 •- radicals due to the efficient trapping of photogenerated electrons in ZnO by rGO.

Uranium series radionuclides in surface waters from the Shu river (Kazakhstan).

The concentrations of (238)U, (234)U, (226)Ra, (210)Po and (210)Pb have been determined in surface waters collected along the course of the Shu River, lying on the border between Kazakhstan and Kyrgyzstan. In the study area, the river runs through some of the largest uranium deposits worldwide, which were actively exploited during the nuclear weapons and nuclear energy programmes of the former Soviet Union. The data show an increasing trend in uranium concentrations downstream the river from the city of Tokmak to the city of Shu, with good correlation between total uranium concentrations and total dissolved solids. Data on uranium isotopes disequilibrium show the presence of technogenic uranium inputs into the Shu River downstream from the city of Karasu, evidenced by a decrease in the measured (234)U/(238)U isotopic ratio from 1.63 in uncontaminated sites to 1.29 in sites affected by past mining activities.