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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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) |
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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 |
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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 |
work_keys_str_mv |
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1718443890165415936 |