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Oxidation of Roxarsone Coupled with Sorptive Removal of the Inorganic Arsenic Released by Iron–Carbon (Fe–C) Microelectrolysis
https://orcid.org/0000-0003-4911-6971
Iron–carbon (Fe–C) microelectrolysis was proposed as a novel method for simultaneous degradation of a model phenylarsenic compound, roxarsone (ROX), in manure leachate and removal of the inorganic arsenic released. The initial rate equation for ROX degradation was determined as r init = 1.55[ROX]1.0[Fe–C]0.9[H+]0.5 (μM/min), at the initial solution pH of 2.0–5.0 and in the presence of overdosed Fe–C filler. A unique advantage of Fe–C microelectrolysis process is that ROX was first reduced to 3-amino-4-hydroxyphenylarsenic acid by the atomic hydrogen generated by cathodic reduction under acidic conditions, which facilitated subsequent oxidative attack by HO•. The iron (hydro)oxide precipitate formed from iron corrosion effectively captured the inorganic arsenic released, reducing the residual arsenic level in the treated water and swine manure leachate to <100 μg/L (standard for irrigation water in China), while the treatment performance was barely affected by the major constitutes of water matrix. The residual level of arsenic in the effluent of a Fe–C microelectrolysis column could be kept consistently below 100 μg/L for 5 months with proper replenishment of the Fe–C filler. The concurrent occurrence of reduction and oxidation reactions and the in situ generation of iron (hydro)oxides make Fe–C microelectrolysis process particularly efficient for treating nitroaromatic compounds and organoarsenicals.
Oxidation of Roxarsone Coupled with Sorptive Removal of the Inorganic Arsenic Released by Iron–Carbon (Fe–C) Microelectrolysis
https://orcid.org/0000-0003-4911-6971
Iron–carbon (Fe–C) microelectrolysis was proposed as a novel method for simultaneous degradation of a model phenylarsenic compound, roxarsone (ROX), in manure leachate and removal of the inorganic arsenic released. The initial rate equation for ROX degradation was determined as r init = 1.55[ROX]1.0[Fe–C]0.9[H+]0.5 (μM/min), at the initial solution pH of 2.0–5.0 and in the presence of overdosed Fe–C filler. A unique advantage of Fe–C microelectrolysis process is that ROX was first reduced to 3-amino-4-hydroxyphenylarsenic acid by the atomic hydrogen generated by cathodic reduction under acidic conditions, which facilitated subsequent oxidative attack by HO•. The iron (hydro)oxide precipitate formed from iron corrosion effectively captured the inorganic arsenic released, reducing the residual arsenic level in the treated water and swine manure leachate to <100 μg/L (standard for irrigation water in China), while the treatment performance was barely affected by the major constitutes of water matrix. The residual level of arsenic in the effluent of a Fe–C microelectrolysis column could be kept consistently below 100 μg/L for 5 months with proper replenishment of the Fe–C filler. The concurrent occurrence of reduction and oxidation reactions and the in situ generation of iron (hydro)oxides make Fe–C microelectrolysis process particularly efficient for treating nitroaromatic compounds and organoarsenicals.
Oxidation of Roxarsone Coupled with Sorptive Removal of the Inorganic Arsenic Released by Iron–Carbon (Fe–C) Microelectrolysis
https://orcid.org/0000-0003-4911-6971
Iron–carbon (Fe–C) microelectrolysis was proposed as a novel method for simultaneous degradation of a model phenylarsenic compound, roxarsone (ROX), in manure leachate and removal of the inorganic arsenic released. The initial rate equation for ROX degradation was determined as r init = 1.55[ROX]1.0[Fe–C]0.9[H+]0.5 (μM/min), at the initial solution pH of 2.0–5.0 and in the presence of overdosed Fe–C filler. A unique advantage of Fe–C microelectrolysis process is that ROX was first reduced to 3-amino-4-hydroxyphenylarsenic acid by the atomic hydrogen generated by cathodic reduction under acidic conditions, which facilitated subsequent oxidative attack by HO•. The iron (hydro)oxide precipitate formed from iron corrosion effectively captured the inorganic arsenic released, reducing the residual arsenic level in the treated water and swine manure leachate to <100 μg/L (standard for irrigation water in China), while the treatment performance was barely affected by the major constitutes of water matrix. The residual level of arsenic in the effluent of a Fe–C microelectrolysis column could be kept consistently below 100 μg/L for 5 months with proper replenishment of the Fe–C filler. The concurrent occurrence of reduction and oxidation reactions and the in situ generation of iron (hydro)oxides make Fe–C microelectrolysis process particularly efficient for treating nitroaromatic compounds and organoarsenicals.
Oxidation of Roxarsone Coupled with Sorptive Removal of the Inorganic Arsenic Released by Iron–Carbon (Fe–C) Microelectrolysis
Xie, Xiande (Autor:in) / Cheng, Hefa (Autor:in)
ACS ES&T Engineering ; 1 ; 1298-1310
10.09.2021
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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