Abstract
This study investigates the electrochemical degradation of N,N-diethyl-m-toluamide (DEET) on PbO2 and Bi-PbO2 anodes. The difference in electrode crystalline structure was responsible for the better DEET degradation and TOC removal on PbO2 than on Bi-PbO2. In 1 M Na2SO4, the degradation efficiency and apparent rate constant (kapp) of DEET oxidation on PbO2 increased with the increase in current density or temperature (activation energy = 24.4 kJ mol−1). The kapp values in DEET-spiked environmental matrixes (municipal wastewater treatment plant secondary effluent (MWTPSE), groundwater (GW), and river water (RW)) were the same (6.05 × 10−4 s−1), but significantly smaller than that in 1 M Na2SO4 (2.23 × 10−3 s−1). The TOC removal efficiency was better in MWTPSE than in RW and GW; however, the mineralization current efficiencies in MWTPSE and RW were similar but higher than that in GW. During electrolysis, the aromaticity was lower in GW than in RW.
Funding
The authors thank the Ministry of Science and Technology (previously National Science Council) of Taiwan for financial support of this research under contract nos. NSC-102-2221-E-020-001-MY3 and NSC-102-2221-E-020-006-MY3.