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      Visible-light-induced photocatalysis and peroxymonosulfate activation over ZnFe 2O 4 fine nanoparticles for degradation of Orange II

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          Abstract

          The coupling effect of photocatalysis and PMS activation remarkably manifested in the eco-friendly ZnFe 2O 4/PMS/vis system for Orange II degradation.

          Abstract

          Refractory and non-biodegradable pollutants produced by industries have inevitably brought great threat to human life. Integrating several kinds of advanced oxidation processes (AOPs) into one system has been proposed to be an efficient strategy to remove such pollutants from the environment at low cost. In this study, magnetic zinc ferrite fine nanoparticles, firstly synthesized by a novel soft chemical solution process, showed super reactivity, good reusability and easy separation ability for visible-light-induced Orange II degradation in an integrated ZnFe 2O 4/PMS (peroxymonosulfate, 2KHSO 5·KHSO 4·K 2SO 4, OXONE) aqueous system. Powder X-ray diffraction, transmission electron microscopy, and 57Fe Mössbauer and X-ray photoelectron spectroscopy were employed to characterize the structure and morphology as well as recognize the physicochemical changes of the fine nanoparticles before and after the reaction. The generated oxidizing intermediates during the degradation process were detected by electron paramagnetic resonance spectroscopy and classic quenching experiments, which confirmed that both sulfate radical (SO 4˙ ) and hydroxyl radical (˙OH) co-existed in the degradation process. The systematic condition experiments further verified the dual functionality of the ZnFe 2O 4/PMS system, which actively acted as a photocatalyst and a PMS activator for dye molecule oxidation under visible light irradiation. This study proves that photocatalysis and PMS activation for remediation of organic pollutants in water can be easily integrated into one system by using zinc ferrite nanoparticles as an environmentally friendly catalyst.

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              Production of sulfate radical from peroxymonosulfate induced by a magnetically separable CuFe2O4 spinel in water: efficiency, stability, and mechanism.

              A simple, nonhazardous, efficient and low energy-consuming process is desirable to generate powerful radicals from peroxymonosulfate (PMS) for recalcitrant pollutant removal. In this work, the production of radical species from PMS induced by a magnetic CuFe(2)O(4) spinel was studied. Iopromide, a recalcitrant model pollutant, was used to investigate the efficiency of this process. CuFe(2)O(4) showed higher activity and 30 times lower Cu(2+) leaching (1.5 μg L(-1) per 100 mg L(-1)) than a well-crystallized CuO at the same dosage. CuFe(2)O(4) maintained its activity and crystallinity during repeated batch experiments. In comparison, the activity of CuO declined significantly, which was ascribed to the deterioration in its degree of crystallinity. The efficiency of the PMS/CuFe(2)O(4) was highest at neutral pH and decreased at acidic and alkaline pHs. Sulfate radical was the primary radical species responsible for the iopromide degradation. On the basis of the stoichiometry of oxalate degradation in the PMS/CuFe(2)O(4), the radical production yield from PMS was determined to be near 1 mol/mol. The PMS decomposition involved an inner-sphere complexation with the oxide's surface Cu(II) sites. In situ characterization of the oxide surface with ATR-FTIR and Raman during the PMS decomposition suggested that surface Cu(II)-Cu(III)-Cu(II) redox cycle was responsible for the efficient sulfate radical generation from PMS.
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                Author and article information

                Journal
                CSTAGD
                Catalysis Science & Technology
                Catal. Sci. Technol.
                Royal Society of Chemistry (RSC)
                2044-4753
                2044-4761
                2016
                2016
                : 6
                : 7
                : 2296-2304
                Affiliations
                [1 ]Mössbauer Effect Data Center & Laboratory of Catalysts and New Materials for Aerospace
                [2 ]Dalian Institute of Chemical Physics
                [3 ]Chinese Academy of Sciences
                [4 ]Dalian 116023
                [5 ]China
                Article
                10.1039/C5CY01735A
                d5b59f5c-a003-47d1-b990-44ab5c58fe63
                © 2016
                History

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