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      Enhanced activation of PMS by a novel Fenton-like composite Fe 3O 4/S-WO 3 for rapid chloroxylenol degradation

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          Abstract

          Chloroxylenol (PCMX) is widely used as disinfectant since the epidemic outbreak due to its effective killing of Covid-19 virus. Its stable chemical properties make it frequently detected in surface water. Herein, we successfully modified Fe 3O 4 nanoparticles with S-WO 3 (X-Fe 3O 4/S-WO 3) to accelerate the Fe 2+/Fe 3+ cycle. The composite has outstanding PCMX degradation and peroxymonosulfate (PMS) decomposition efficiency over a wide pH range (3.0 ∼ 9.0). 80-Fe 3O 4/S-WO 3/PMS system not only increased PMS decomposition efficiency from 27.7% to 100.0%, but also realized an enhancement of PCMX degradation efficiency by 16 times in comparison with that of Fe 3O 4 alone. The catalyst utilization efficiency reached 0.3506 mmol∙g −1∙min −1 which stands out among most Fenton-like catalysts. The composite has excellent degradation ability to a variety of emerging pollutants, such as antibiotics, drugs, phenols and endocrine disrupters, and at least a 90% removal efficiency reached in 10 min. The degradation of PCMX was dominated by HO , SO 4 •− and 1O 2. The degradation pathways of PCMX were analyzed in detail. The component WS 2 in S-WO 3 plays a co-catalytic role instead of WO 3. And the exposed active W 4+ surf. efficiently enhanced the Fe 3+/Fe 2+ cycle, thereby complete PMS decomposition and high catalytic efficiency were achieved. Our findings clarify that applying two-dimensional transition metal sulfide WS 2 to modify heterogeneous Fe 3O 4 is a feasible strategy to improve Fenton-like reaction and provide a promising catalyst for PCMX degradation.

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          Most cited references59

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

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            Degradation of organic contaminants in water with sulfate radicals generated by the conjunction of peroxymonosulfate with cobalt.

            A highly efficient advanced oxidation process for the destruction of organic contaminants in water is reported. The technology is based on the cobalt-mediated decomposition of peroxymonosulfate that leads to the formation of very strong oxidizing species (sulfate radicals) in the aqueous phase. The system is a modification of the Fenton Reagent, since an oxidant is coupled with a transition metal in a similar manner. Sulfate radicals were identified with quenching studies using specific alcohols. The study was primarily focused on comparing the cobalt/peroxymonosulfate (Co/PMS) reagent with the traditional Fenton Reagent [Fe(II)/H2O2] in the dark, at the pH range 2.0-9.0 with and without the presence of buffers such as phosphate and carbonate. Three model contaminants that show diversity in structure were tested: 2,4-dichlorophenol, atrazine, and naphthalene. Cobalt/peroxymonosulfate was consistently proven to be more efficient than the Fenton Reagent for the degradation of 2,4-dichlorophenol and atrazine, at all the conditions tested. At high pH values, where the efficiency of the Fenton Reagent was diminished, the reactivity of the Co/PMS system was sustained at high values. When naphthalene was treated with the two oxidizing systems in comparison, the Fenton Reagent demonstrated higher degradation efficiencies than cobalt/peroxymonosulfate at acidic pH, but, at higher pH (neutral), the latter was proven much more effective. The extent of mineralization, as total organic carbon removed,was also monitored, and again the Co/PMS reagent demonstrated higher efficiencies than the Fenton Reagent. Cobalt showed true catalytic activity in the overall process, since extremely low concentrations (in the range of microg/L) were sufficient for the decomposition of the oxidant and thus the radical generation. The advantage of Co/PMS compared to the traditional Fenton Reagent is attributed primarily to the oxidizing strength of the radicals formed, since sulfate radicals are stronger oxidants than hydroxyl and the thermodynamics of the transition-metal-oxidant coupling.
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              Activation of Peroxymonosulfate by Benzoquinone: A Novel Nonradical Oxidation Process

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                Author and article information

                Journal
                Chem Eng J
                Chem Eng J
                Chemical Engineering Journal
                Elsevier B.V.
                1385-8947
                1385-8947
                19 May 2022
                15 October 2022
                19 May 2022
                : 446
                : 137067
                Affiliations
                [a ]State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, No. 130 Meilong Road, Shanghai 200237, China
                [b ]Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China
                Author notes
                [* ]Corresponding author at: State Environmental Protection Key Laboratory of Environmental Risk Assessment and Control on Chemical Process, East China University of Science and Technology, No. 130 Meilong Road, Shanghai 200237, China.
                Article
                S1385-8947(22)02559-1 137067
                10.1016/j.cej.2022.137067
                9700388
                7cd5e13e-4152-4004-849c-33b1cfb308bd
                © 2022 Elsevier B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 4 March 2022
                : 15 May 2022
                : 16 May 2022
                Categories
                Article

                peroxymonosulfate,fe3o4,ws2,chloroxylenol
                peroxymonosulfate, fe3o4, ws2, chloroxylenol

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