Lauridsencarpenter1755

Due to the reduction of permanganate and stabilization of the in situ formed colloidal MnO2 by water matrix, the oxidation rate of pollutant in real water is higher than that in pure water.Parabens are a class of compounds primarily used as antimicrobial preservatives in pharmaceutical products, cosmetics, and foodstuff. Their widely used field leads to increasing concentrations detected in various environmental matrices like water, soil, and sludges, even detected in human tissue, blood, and milk. Treatment techniques, including chemical advanced oxidation, biological degradation, and physical adsorption processes, have been widely used to complete mineralization or to degrade parabens into less complicated byproducts. All kinds of processes were reviewed to give a completed picture of parabens removal. In light of these treatment techniques, advanced photocatalysis, which is emerging rapidly and widely as an economical, efficient, and environmentally-friendly technique, has received considerable attention. TiO2-based and non-TiO2-based photocatalysts play an essential role in parabens degradation. The effect of experimental parameters, such as the concentration of targeted parabens, concentration of photocatalyst, reaction time, and initial solution pH, even the presence of radical scavengers, are surveyed and compared from the literature. Some representative parabens such as methylparaben, propylparaben, and benzylparaben have been successfully studied the reaction pathways and their intermediates in their degradation process. As reported in the literature, the degradation of parabens involves the production of highly reactive species, mainly hydroxyl radicals. These reactive radicals would attack the paraben preservatives, break, and finally mineralize them into simpler inorganic and nontoxic molecules. Concluding perspectives on the challenges and opportunities for photocatalysis toward parabens remediation are also intensively highlighted.Photoinduced reduction and oxidation, the important processes in photocatalytic water splitting and organic degradation, have generated increasing interest to address the energy and environmental issues. In this review, the recent developments in bandgap and interfacial engineering for enhanced light absorption, efficient charge separation and interfacial reaction are focused toward the applications in photocatalytic water splitting and organic degradation. In photoinduced reduction for hydrogen evolution, three major strategies are discussed cocatalysts, sacrificial agents and heterojunctions. In photoinduced oxidation for organic degradation, three types of emerging pollutants of current concerns are highlighted organic dyes, pharmaceuticals and volatile organic compounds. The key challenges of promising photocatalysts are discussed for future development and practical application.Bubble-propelled sulfur-encapsulated NaX zeolite (S-NaX) micromotors were developed for the selective removal of cesium from high-salt conditions with accelerated cleanup times. NaX was first modified with sulfur to provide additional Lewis acid-base interactions with Cs+ for enhanced Cs+ selectivity, and then Pt was half-deposited on S-NaX for bubble propulsion via the catalytic decomposition of H2O2. The average velocity of the resulting S-NaX/Pt micromotors in 5 wt% H2O2 is 39.7 ± 17.1 μm/s, which is higher than that of a previously reported Cs adsorbent micromotor (35.4 μm/s). The Cs+ ion-exchange kinetics of the S-NaX micromotor is 1.32 times higher than that of the NaX micromotor in a 5 wt% H2O2 solution where the molar ratio of Na+ to Cs+ is 200, even though the sulfur in the S-NaX micromotor causes an adverse effect on the propulsion speed due to the sulfur poisoning effect. Moreover, the S-NaX micromotor in simulated groundwater also exhibited excellent Cs+ removal performance with distribution coefficient (Kd) values at least 3.2 times higher than those of the nonpropelled S-NaX and NaX micromotor, demonstrating the great potential for the treatment of radioactive Cs+-contaminated water.Bovine milk is a nutritious food commodity extensively produced and consumed in Punjab, Pakistan. This study assesses the concentration profile of organochlorine pesticides (OCP; 18 compounds) in buffaloes and cow's milk in eight major districts of Punjab, Pakistan and the potential impacts of such exposure. The total OCPs in buffaloes and cow's milk samples ranged from 3.93 to 27.63 ng mL-1 and 14.64-77.93 ng mL-1 respectively. The overall pattern of mean OCPs concentration in buffaloes and cows milk showed that Hexachlorocyclohexanes (HCHs) are predominant followed by Heptachlors and Dichlorodiphenyltrichloroethane (DDTs). So far, the concentration profile depicted that ∑HCHs, ∑DDTs and ∑Heptachlors did not exceed the maximum residual limits set for buffaloes and cow's milk. The spatial trends in terms of cluster analysis depicted significant variation (p > 0.05) among the districts in one cluster probably owing to local conditions. Furthermore, recently used DDTs were also identified at some of the selected districts. The risk assessment suggests that the estimated daily intake for each OCP was in accordance with the acceptable daily intake, thus single compound exposure does not pose a significant carcinogenic risk. However, the hazard ratios indicated that the values for ∑DDTs posed risk in adults consuming cow's milk whereas children may face carcinogenic risk on the consumption of both buffalo and cow's milk. The risk may be altered where mixture is considered, furthermore, regarding carcinogenic risks a continuous monitoring based ecological analysis is recommended in the future.Phytoexcretion is a novel strategy to remediate cadmium (Cd) pollution by leaf excretion in tall fescue (Festuca arundinacea), which involves the processes of Cd leaf excretion, root-to-leaf translocation, and root uptake. A hydroponic experiment was designed to investigate a series of 11 zinc (Zn) concentrations on Cd leaf excretion in tall fescue under 75 μM Cd stress. CCT245737 The results showed that the promotions of Zn on Cd leaf excretion, root-to-leaf translocation, and leaf accumulation were concentration-dependent in tall fescue. Zn treatments at 90 and 135 μM resulted in the highest Cd leaf excretion with 118.1 and 123.6 mg/kg of Cd excretion amount and 27.0 and 26.6% of excretion ratio, which were 2.6 and 2.7 fold of the control (15 μM of Zn), respectively. Cd leaf excretion was decreased when Zn treatments reached 180 μM, which could be toxic to plants as indicated by the decline of plant biomass. Zn also promoted leaf Cd accumulation and Cd translocation from roots to leaves and reached the highest at 90 and 180 μM respectively.