Title of article :
Electrochemical degradation of tricyclazole in aqueous solution using Ti/SnO2–Sb/PbO2 anode
Author/Authors :
Zhong، نويسنده , , Congqiang and Wei، نويسنده , , Kajia and Han، نويسنده , , Weiqing and Wang، نويسنده , , Lianjun and Sun، نويسنده , , Xiuyun and Li، نويسنده , , Jiansheng، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
7
From page :
68
To page :
74
Abstract :
The electrochemical degradation of the fungicide tricyclazole(TC) in aqueous solution on a Ti/SnO2–Sb/PbO2 anode was investigated for the first time. Effect of key operating parameters such as the current density, the initial pH, the initial concentration of supporting electrolyte and TC was studied on the degradation efficiency. The current density and concentration of Na2SO4 exerted a prominent effect on degradation rate, and no significant effect of initial pH on TC mineralization and COD removal was observed. The efficiency of TC and COD removal decreased with increasing initial TC concentration, from 0.53 to 1.06 mM. Kinetic analyses indicated that the electrochemical degradation of TC was a pseudo-first-order reaction. The apparent rate constant (k1) value of TC oxidation was determined as 1.50 × 10−4 s−1 at 25 mA cm−2 in the presence of 7.0 g L−1 Na2SO4 in acidic media (pH: 5.0). The mineralization intermediates were analyzed by chromatographic techniques, several aromatic intermediates and short-chain carboxylic acids generated along the reaction time had been quantified. Heteroatom oxidation products like NO 2 - , NO 3 - had been quantified and explanations of their release were proposed. Finally, considering the identified reaction intermediates, a pathway for electrocatalytic degradation of TC in aqueous solution was proposed.
Keywords :
Electrochemical oxidation , Aromatic products , Generated carboxylic acids , tricyclazole , Wastewater treatment
Journal title :
Journal of Electroanalytical Chemistry
Serial Year :
2013
Journal title :
Journal of Electroanalytical Chemistry
Record number :
1677438
Link To Document :
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