期刊
ELECTROCHIMICA ACTA
卷 387, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2021.138521
关键词
Electrochemical advanced oxidation processes (EAOPs); Boron-doped diamond anodes (BDD); Water treatment; Chlorine volatile species; Oxalic acid; Persistent organic pollutants
资金
- Green Talents award from the BMBF Germany
Understanding the role of supporting electrolytes in the electrochemical oxidation of organics is essential for water treatment strategies. Differential electrochemical mass spectrometry (DEMS) can be used as an electroanalytical tool to measure engineering figures of merit and reveal the influence of coexisting ionic species on oxidation reactions. Higher efficiency in oxidation reactions was observed with (OH)-O-center dot radicals-mediated oxidation at BDD electrode.
A fundamental understanding of the role of supporting electrolytes on the electrochemical oxidation of organics is essential to develop strategies for water treatment applications. This work completes research efforts of literature by evaluating directly the evolution of CO2 at the BDD electrode as a result of the mineralization of oxalic acid. The use of differential electrochemical mass spectrometry (DEMS) as an electroanalytical tool enables online measurement of engineering figures of merit of electrochemical advanced oxidation technologies and unravels the influence of coexisting ionic species in solution. Furthermore, the oxidation of CO is conducted to elucidate how different electrogenerated oxidants may be involved in oxidation reactions. CO2 current efficiencies calculated for the oxidation of CO were higher for electrolytes where more (OH)-O-center dot radicals are available for the oxidation of CO which suggests the (OH)-O-center dot radicals-mediated CO oxidation at BDD. Thereby, higher efficiency was observed in the perchlorate electrolyte than nitrate, sulfate, and chloride electrolytes. The decrease in the CO2 current efficiencies in the other electrolytes is explained by the competitive consumption of (OH)-O-center dot due to the formation of other oxidants such as SO4 center dot- Cl-center dot, other chlorine active species, and possibly also NO4-. CO2 was the predominant oxidation product during the oxidation of oxalic acid in all electrolytes with a higher oxidation capability in the perchlorate and chloride electrolytes than nitrate and sulfate. These results show that the oxidation of oxalic acid is mediated by (OH)-O-center dot, direct charge transfer, as well as by other oxidants produced at the BDD at different electrolytes. (C) 2021 Elsevier Ltd. All rights reserved.
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