Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells

To explore the electrochemical conversion of arsenic at different voltages and pH, an open separated electrolytic cell with a platinum anode and a graphite cathode was selected for this paper. The form and concentration of arsenic in the anodic cell and cathodic cell were detected. Experimental resu...

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Autores principales: Yanyan Qin, Yanping Cui, Zhengwei Zhou, Ya Gao, Lidan Lei, Xiaoyan Shi
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Publicado: IWA Publishing 2021
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Acceso en línea:https://doaj.org/article/e86f3195daa24dbeba86b602fc1c1add
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spelling oai:doaj.org-article:e86f3195daa24dbeba86b602fc1c1add2021-11-06T07:05:15ZElectrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells1606-97491607-079810.2166/ws.2020.261https://doaj.org/article/e86f3195daa24dbeba86b602fc1c1add2021-02-01T00:00:00Zhttp://ws.iwaponline.com/content/21/1/46https://doaj.org/toc/1606-9749https://doaj.org/toc/1607-0798To explore the electrochemical conversion of arsenic at different voltages and pH, an open separated electrolytic cell with a platinum anode and a graphite cathode was selected for this paper. The form and concentration of arsenic in the anodic cell and cathodic cell were detected. Experimental results proved that at 40.0 V, As(III) in an acid electrolyte in the cathodic cell was firstly mainly reduced to AsH3 with trace As(0) as intermediate. As the electrolysis time arrived at 27 min, pH in the cathodic cell jumped suddenly from acidity to alkalinity, accompanied by the majority of the remaining As(III) converting to As(V) for an instant. As time went on, As(III) and As(V) remained almost unchanged at the ratio of 1:3, and the reduction of As(III) became extremely weak in the alkaline environment. When pH in the cathodic tank was adjusted to keep it acid, As(III) was eventually converted to AsH3. Compared with high voltage, at a low voltage of 1.0 V the cathode failed to achieve the potential of As(III) reduction and As(III) was eventually oxidized to As(V) in the acid catholyte. Electrochemical oxidation of As(III) in the open cathodic cell was likely caused by in-situ generation of peroxide from electrochemical reduction of O2. Theoretical support for electrochemical oxidation of As(III) on a carbon cathode in neutral and weak alkaline media is provided in this study.Yanyan QinYanping CuiZhengwei ZhouYa GaoLidan LeiXiaoyan ShiIWA Publishingarticlearsenicconversion pathwaysexisting formgraphite cathodeseparated electrolytic cellWater supply for domestic and industrial purposesTD201-500River, lake, and water-supply engineering (General)TC401-506ENWater Supply, Vol 21, Iss 1, Pp 46-58 (2021)
institution DOAJ
collection DOAJ
language EN
topic arsenic
conversion pathways
existing form
graphite cathode
separated electrolytic cell
Water supply for domestic and industrial purposes
TD201-500
River, lake, and water-supply engineering (General)
TC401-506
spellingShingle arsenic
conversion pathways
existing form
graphite cathode
separated electrolytic cell
Water supply for domestic and industrial purposes
TD201-500
River, lake, and water-supply engineering (General)
TC401-506
Yanyan Qin
Yanping Cui
Zhengwei Zhou
Ya Gao
Lidan Lei
Xiaoyan Shi
Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells
description To explore the electrochemical conversion of arsenic at different voltages and pH, an open separated electrolytic cell with a platinum anode and a graphite cathode was selected for this paper. The form and concentration of arsenic in the anodic cell and cathodic cell were detected. Experimental results proved that at 40.0 V, As(III) in an acid electrolyte in the cathodic cell was firstly mainly reduced to AsH3 with trace As(0) as intermediate. As the electrolysis time arrived at 27 min, pH in the cathodic cell jumped suddenly from acidity to alkalinity, accompanied by the majority of the remaining As(III) converting to As(V) for an instant. As time went on, As(III) and As(V) remained almost unchanged at the ratio of 1:3, and the reduction of As(III) became extremely weak in the alkaline environment. When pH in the cathodic tank was adjusted to keep it acid, As(III) was eventually converted to AsH3. Compared with high voltage, at a low voltage of 1.0 V the cathode failed to achieve the potential of As(III) reduction and As(III) was eventually oxidized to As(V) in the acid catholyte. Electrochemical oxidation of As(III) in the open cathodic cell was likely caused by in-situ generation of peroxide from electrochemical reduction of O2. Theoretical support for electrochemical oxidation of As(III) on a carbon cathode in neutral and weak alkaline media is provided in this study.
format article
author Yanyan Qin
Yanping Cui
Zhengwei Zhou
Ya Gao
Lidan Lei
Xiaoyan Shi
author_facet Yanyan Qin
Yanping Cui
Zhengwei Zhou
Ya Gao
Lidan Lei
Xiaoyan Shi
author_sort Yanyan Qin
title Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells
title_short Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells
title_full Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells
title_fullStr Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells
title_full_unstemmed Electrochemical conversion pathways and existing morphology of arsenic(III) in anode-cathode separated electrolytic cells
title_sort electrochemical conversion pathways and existing morphology of arsenic(iii) in anode-cathode separated electrolytic cells
publisher IWA Publishing
publishDate 2021
url https://doaj.org/article/e86f3195daa24dbeba86b602fc1c1add
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AT yanpingcui electrochemicalconversionpathwaysandexistingmorphologyofarseniciiiinanodecathodeseparatedelectrolyticcells
AT zhengweizhou electrochemicalconversionpathwaysandexistingmorphologyofarseniciiiinanodecathodeseparatedelectrolyticcells
AT yagao electrochemicalconversionpathwaysandexistingmorphologyofarseniciiiinanodecathodeseparatedelectrolyticcells
AT lidanlei electrochemicalconversionpathwaysandexistingmorphologyofarseniciiiinanodecathodeseparatedelectrolyticcells
AT xiaoyanshi electrochemicalconversionpathwaysandexistingmorphologyofarseniciiiinanodecathodeseparatedelectrolyticcells
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