TY - JOUR
T1 - Electrochemical oxidation of ethylenediaminetetraacetic acid (EDTA) on BDD electrodes
T2 - Application to wastewater treatment
AU - Ouattara, Lassine
AU - Duo, Ilaria
AU - Diaco, Thomas
AU - Anggraningrum, Ivandini Tribidasari
AU - Honda, Kensuke
AU - Rao, Tata
AU - Fujishima, Akira
AU - Comninellis, Christos
PY - 2003
Y1 - 2003
N2 - The electrochemical oxidation of ethylenediaminetetraacetic acid (EDTA) was investigated at boron-doped diamond (BDD) electrodes. Cyclic voltammetry in the potential region of water stability showed that EDTA is oxidised in an irreversible two-electron-transfer mechanism. No fouling phenomena were noticed on the electrode surface. At high anode potential, an oxidation mechanism of EDTA involving hydroxyl radicals, formed during water discharge, was proposed. Moreover, the model previously developed for organic oxidation at nonactive anodes was successfully used in order to predict the trends of chemical oxygen demand (COD) and instantaneous current efficiency (ICE) during EDTA oxidation on BDD electrodes. Bulk electrolyses were performed under different regimes. The very good fit between the experimental results and theoretical values confirmed that EDTA oxidation at the BDD electrode in the potential region of electrolyte decomposition was a fast reaction.
AB - The electrochemical oxidation of ethylenediaminetetraacetic acid (EDTA) was investigated at boron-doped diamond (BDD) electrodes. Cyclic voltammetry in the potential region of water stability showed that EDTA is oxidised in an irreversible two-electron-transfer mechanism. No fouling phenomena were noticed on the electrode surface. At high anode potential, an oxidation mechanism of EDTA involving hydroxyl radicals, formed during water discharge, was proposed. Moreover, the model previously developed for organic oxidation at nonactive anodes was successfully used in order to predict the trends of chemical oxygen demand (COD) and instantaneous current efficiency (ICE) during EDTA oxidation on BDD electrodes. Bulk electrolyses were performed under different regimes. The very good fit between the experimental results and theoretical values confirmed that EDTA oxidation at the BDD electrode in the potential region of electrolyte decomposition was a fast reaction.
KW - Boron-doped diamond
KW - Bulk electolyses
KW - Electrochemical oxidation
KW - Ethylenediaminetetraacetic acid oxidation
KW - Hydroxyl radical
UR - http://www.scopus.com/inward/record.url?scp=0038672047&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0038672047
SN - 1344-9931
VL - 13
SP - 97
EP - 108
JO - New Diamond and Frontier Carbon Technology
JF - New Diamond and Frontier Carbon Technology
IS - 2
ER -