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      In situ chemical oxidation: peroxide or persulfate coupled with membrane technology for wastewater treatment

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          Abstract

          Three membrane-coupled PS/H 2O 2-based ISCO processes for wastewater treatment are fully summarized for the first time and their main challenges are discussed, providing important directions for their practical industrial applications in the future.

          Abstract

          Refractory organic pollutants in wastewater have the characteristics of persistence and toxicity, which seriously threaten the health and safety of humans and other organisms. Many researchers have committed to developing effective wastewater treatment technologies in the past few decades. The coupling of membrane technology with persulfate/peroxide-based in situ chemical oxidation (ISCO) not only can successfully overcome the shortcomings of the two single technologies, such as membrane fouling and difficult reuse of some catalysts, but also effectively achieve complementary advantages of pollutant filtration and degradation. Therefore, it has received extensive attention from researchers and is expected to be large-scale applied to actual wastewater treatment. In this review, according to different membrane materials, the common membrane types are briefly summarized, and then the synthesis methods of the catalytic membrane are introduced. In addition, various process configurations coupling membrane filtration with ISCO are researched. Two main modes of the coupling processes can be defined: (i) a one-pot coupling process which simultaneously oxidizes and separates organic pollutants; (ii) a two-stage coupling process, including a pretreatment stage for the removal of foulant forming molecules in the membrane feed water, and a post-treatment stage to further degrade the pollutants of membrane concentrate and permeation fluid. Finally, the major challenges and application prospects of membrane filtration coupled with ISCO in wastewater treatment are discussed.

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          Activation of persulfate (PS) and peroxymonosulfate (PMS) and application for the degradation of emerging contaminants

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            Progress in the production and modification of PVDF membranes

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              Persulfate activation on crystallographic manganese oxides: Mechanism of singlet oxygen evolution for nonradical selective degradation of aqueous contaminants

              Minerals and transitional metal oxides of earth-abundant elements are desirable catalysts for in situ chemical oxidation in environmental remediation. However, catalytic activation of peroxydisulfate (PDS) by manganese oxides was barely investigated. In this study, one-dimension manganese dioxides (α- and β-MnO2) were discovered as effective PDS activators among the diverse manganese oxides for selective degradation of organic contaminants. Compared with other chemical states and crystallographic structures of manganese oxide, β-MnO2 nanorods exhibited the highest phenol degradation rate (0.044 min-1, 180 min) by activating PDS. A comprehensive study was conducted utilizing electron paramagnetic resonance, chemical probes, radical scavengers, and different solvents to identity the reactive oxygen species (ROS). Singlet oxygen (1O2) was unveiled to be the primary ROS, which was generated by direct oxidation or recombination of superoxide ions and radicals from a metastable manganese intermediate at neutral pH. The study dedicates to the first mechanistic study into PDS activation over manganese oxides and provides a novel catalytic system for selective removal of organic contaminants in wastewater.
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                Author and article information

                Contributors
                Journal
                JMCAET
                Journal of Materials Chemistry A
                J. Mater. Chem. A
                Royal Society of Chemistry (RSC)
                2050-7488
                2050-7496
                May 25 2021
                2021
                : 9
                : 20
                : 11944-11960
                Affiliations
                [1 ]College of Environmental Science and Engineering
                [2 ]Hunan University
                [3 ]Changsha
                [4 ]PR China
                [5 ]Key Laboratory of Environmental Biology and Pollution Control
                Article
                10.1039/D1TA01063H
                da35bd6c-2e49-4260-b087-074d1d9bb9aa
                © 2021

                http://rsc.li/journals-terms-of-use

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