Electrochemical degradation of enrofloxacin by lead dioxide anode: Kinetics, mechanism and toxicity evaluation

2017 ◽  
Vol 326 ◽  
pp. 911-920 ◽  
Author(s):  
Chong Wang ◽  
Lifeng Yin ◽  
Zesheng Xu ◽  
Junfeng Niu ◽  
Li-An Hou
2013 ◽  
Vol 827 ◽  
pp. 30-33
Author(s):  
Cong Qiang Zhong ◽  
Yun Long Sun ◽  
Ying Guan ◽  
Wei Qing Han ◽  
Lian Jun Wang

The electrochemical degradation of tricyclazole (TC) in aqueous solution on Ti/SnO2Sb/PbO2anodes was investigated. The degradation efficiency and mineralization rate was studied. Kinetic analyses indicated that the electrochemical degradation followed a pseudo-first-order reaction. The mineralization intermediates were analyzed by chromatographic techniques. Finally, a pathway for electrochemical degradation of TC in aqueous medium was proposed.


1989 ◽  
Vol 42 (9) ◽  
pp. 1527 ◽  
Author(s):  
TH Randle ◽  
AT Kuhn

Lead dioxide is a strong oxidizer in sulfuric acid, consequently electrochemical oxidation of solution species at a lead dioxide anode may occur by a two-step, C-E process (chemical oxidation of solution species by PbO2 followed by electrochemical regeneration of the reduced lead dioxide surface). The maximum rate of each step has been determined in sulfuric acid for specified lead dioxide surfaces and compared with the rates observed for the electrochemical oxidation of cerium(III) and manganese(II) on the same electrode surfaces. While the rate of electrochemical oxidation of a partially reduced PbO2 surface may be sufficient to support the observed rates of CeIII and MnII oxidation at the lead dioxide anode, the rate of chemical reaction between PbO2 and the reducing species is not. Hence it is concluded that the lead dioxide electrode functions as a simple, 'inert' electron-transfer agent during the electrochemical oxidation of CellI and MnII in sulfuric acid. In general, it will most probably be the rate of the chemical step which determines the feasibility or otherwise of the C-E mechanism.


1958 ◽  
Vol 105 (2) ◽  
pp. 100 ◽  
Author(s):  
J. C. Grigger ◽  
H. C. Miller ◽  
F. D. Loomis

1989 ◽  
Vol 42 (2) ◽  
pp. 229 ◽  
Author(s):  
TH Randle ◽  
AT Kuhn

The electrolytic oxidation reactions of cerium(III) and manganeseII) in sulfuric acid have been used as probes to investigate the mechanism of the lead dioxide anode. The kinetics observed for such reactions at the lead dioxide surface provide no direct support for the proposal that the lead dioxide anode functions by a sequential 'two-step' mechanism (heterogeneous chemical oxidation of solution species followed by electrochemical oxidation of the reduced lead dioxide surface); rather the kinetics show characteristics similar to those observed previously for the oxidation of cerium(III) and manganese(II) at the platinum electrode, suggesting that the lead dioxide surface functions as a simple, 'inert' electron-transfer agent.


1965 ◽  
Vol 10 (12) ◽  
pp. 1185-1187 ◽  
Author(s):  
M.S.V. Pathy ◽  
H.V.K. Udupa

2014 ◽  
Vol 280 ◽  
pp. 579-587 ◽  
Author(s):  
Aleksandra Fabiańska ◽  
Anna Białk-Bielińska ◽  
Piotr Stepnowski ◽  
Stefan Stolte ◽  
Ewa Maria Siedlecka

Sign in / Sign up

Export Citation Format

Share Document