2 research outputs found

    Understanding the Reduction Kinetics of Aqueous Vanadium(V) and Transformation Products Using Rotating Ring-Disk Electrodes

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    Vanadium­(V) is an emerging contaminant in the most recent Environmental Protection Agency’s candidate contaminant list (CCL4). The redox chemistry of vanadium controls its occurrence in the aquatic environment, but the impact of vanadium­(V) speciation on the redox properties remains largely unknown. This study utilized the rotating ring-disk electrode technique to examine the reduction kinetics of four pH- and concentration-dependent vanadium­(V) species in the presence and the absence of phosphate. Results showed that the reduction of VO<sub>2</sub><sup>+</sup>, H<sub><i>x</i></sub>V<sub>4</sub>O<sub>12+<i>x</i></sub><sup>(4+<i>x</i>)–</sup> (V<sub>4</sub>), and HVO<sub>4</sub><sup>2–</sup> proceeded via a one-electron transfer, while that of Na<sub><i>x</i></sub>H<sub><i>y</i></sub>V<sub>10</sub>O<sub>28</sub><sup>(6–<i>x</i>–<i>y</i>)–</sup> (V<sub>10</sub>) underwent a two-electron transfer. Koutecky–Levich and Tafel analyses showed that the intrinsic reduction rate constants followed the order of V<sub>10</sub> > VO<sub>2</sub><sup>+</sup> > V<sub>4</sub> > HVO<sub>4</sub><sup>2–</sup>. Ring-electrode collection efficiency indicated that the reduction product of V<sub>10</sub> was stable, while those of VO<sub>2</sub><sup>+</sup>, HVO<sub>4</sub><sup>2–</sup>, and V<sub>4</sub> had short half-lives that ranged from milliseconds to seconds. With molar ratios of phosphate to vanadium­(V) varying from 0 to 1, phosphate accelerated the reduction kinetics of V<sub>10</sub> and V<sub>4</sub> and enhanced the stability of the reduction products of VO<sub>2</sub><sup>+</sup>, V<sub>4</sub>, and HVO<sub>4</sub><sup>2–</sup>. This study suggests that phosphate complexation could enhance the reductive removal of vanadium­(V) and inhibit the reoxidation of its reduction product in water treatment

    An Outward Coating Route to CuO/MnO<sub>2</sub> Nanorod Array Films and Their Efficient Catalytic Oxidation of Acid Fuchsin Dye

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    An outward coating method has been successfully employed to prepare CuO/MnO<sub>2</sub> nanorod array films based on the impregnation of Cu­(OH)<sub>2</sub> nanorod array films with manganese nitrate aqueous solution and heat post-treatment. The as-prepared CuO/MnO<sub>2</sub> nanorod array films as heterogeneous catalysts successfully address such issues as easy agglomeration, difficult separation, and possible secondary pollution related to powder catalysts. Furthermore, they exhibit catalytic oxidation activity for the degradation of acid fuchsin (AF) dye in aqueous solution superior to that of bare CuO nanorod array films in the presence of H<sub>2</sub>O<sub>2</sub>, because of the synergistic effects of both CuO and MnO<sub>2</sub>. The effects of the initial concentration of aqueous AF solution and H<sub>2</sub>O<sub>2</sub> dosage on the catalytic oxidation performance were evaluated, indicating that the degradation ratio of AF can reach up to 94.05%. Life-cycle performance and scaleup of the catalytic oxidative degradation process demonstrate the durability and potential engineering application of CuO/MnO<sub>2</sub> nanorod array films in dye wastewater treatment
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