Degradation of Tetracycline by Electrochemical Oxidation Using Composite DSA Electrode

2012 ◽  
Author(s):  
Guoting Li ◽  
Yunxia Li ◽  
Jing Chen
Keyword(s):  
Electrochemical Oxidation ◽  
Dsa Electrode

scholarly journals Electrochemical Oxidation of Ethinylestradiol on a Commercial Ti/Ru0.3 Ti0.7O2 DSA Electrode

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Karla M. Vieira ◽  
Clésia C. Nascentes ◽  
Artur J. Motheo ◽  
Rodinei Augusti
Keyword(s):  
Reaction Time ◽  
Electrochemical Oxidation ◽  
Degradation Products ◽  
Electrochemical Treatment ◽  
Flow Cell ◽  
Constant Current ◽  
Direct Infusion ◽  
Degradation Rates ◽  
Dsa Electrode ◽  
Methanolic Medium

The electrochemical oxidation of the hormone ethinylestradiol in an aqueous-methanolic medium by the application of a constant current of 40 mA cm−2 in a flow cell with a commercial Ti/Ru0.3 Ti0.7O2 electrode was evaluated. The effect caused by the use of NaCl as a support electrolyte was also investigated. Hence, HPLC-UV analyses revealed that ethinylestradiol was almost totally consumed after a 60 min reaction time in the presence of NaCl. Conversely, much lower degradation rates were obtained when NaCl was not employed. Moreover, direct infusion ESI-MS and GC-MS analysis revealed that apparently no degradation products had been formed under these conditions. Hence, this study clearly demonstrated that such electrochemical treatment can be efficiently used to promote the complete degradation (and probably mineralization) of the hormone ethinylestradiol.

Electrochemical oxidation of 1H,1H,2H,2H-perfluorooctane sulfonic acid (6:2 FTS) on DSA electrode: Operating parameters and mechanism

2014 ◽  
Vol 26 (8) ◽  
pp. 1733-1739 ◽  
Author(s):  
Qiongfang Zhuo ◽  
Xiang Li ◽  
Feng Yan ◽  
Bo Yang ◽  
Shubo Deng ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Sulfonic Acid ◽  
Operating Parameters ◽  
Dsa Electrode

ELECTROCHEMICAL OXIDATION OF NITROGEN (II) OXIDE IN THE NEUTRAL MEDIUM

THE BULLETIN ◽  
2019 ◽  
Vol 2 (378) ◽  
Author(s):  
Abduali Baeshov ◽  
Gulnar Aibolova ◽  
Elmira Tuleshova ◽  
M. A. Ozler
Keyword(s):  
Electrochemical Oxidation ◽  
Neutral Medium

Electrochemical Oxidation of Hydrazine in Membraneless Fuel Cells

2014 ◽  
Vol 5 (3) ◽  
pp. 73-81 ◽  
Author(s):  
S. Durga ◽  
K. Ponmani ◽  
S. Kiruthika ◽  
B. Muthukumaran
Keyword(s):  
Fuel Cells ◽  
Electrochemical Oxidation ◽  
Membraneless Fuel Cells

Electrochemical Oxidation of Perfluorooctanesulfonate by Magnéli Phase Ti4O7 Electrode in the Presence of Trichloroethylene

2020 ◽  
Vol 1 (4) ◽  
Author(s):  
Peizeng Yang ◽  
Yaye Wang ◽  
Junhe Lu ◽  
Viktor Tishchenko ◽  
Qingguo Huang ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Current Density ◽  
First Order ◽  
Degradation Rates ◽  
Oxidation Technology ◽  
Magnéli Phase ◽  
Polyfluoroalkyl Substances ◽  
Titanium Suboxide ◽  
Gas Tight ◽  
Magneli Phase

This study examined the degradation of perfluorooctanesulfonate (PFOS) in electrochemical oxidation (EO) processes in the presence of trichloroethylene (TCE). The EO experiment was performed in a gas-tight reactor using Magnéli phase titanium suboxide (Ti4O7) as the anode. The experimental data demonstrated that 75% of PFOS (2 μM) was degraded at 10 mA/cm2 current density in 30 min without TCE present in the solution, while the presence of 76 μM TCE apparently inhibited the degradation of PFOS, reducing its removal down to 53%. Defluorination ratio suggested that PFOS was significantly mineralized upon EO treatment, and it appeared to be not influenced by the presence of TCE. The respective pseudo-first order rate constants (kobs) of PFOS removal were 0.0471 and 0.0254 min-1 in the absence and presence of TCE. The degradation rates of both PFOS and TCE increased with current density rising from 2.5 to 20 mA/cm2. In the presence of TCE, chloride, chlorate, and perchlorate were formed that accounted for 79.7 %, 5.53%, and 1.51% of the total chlorine at 60 min. This work illustrates the promise of the Magnéli phase Ti4O7 electrode based electrochemical oxidation technology for degrading per- and polyfluoroalkyl substances (PFASs) and co-contaminants in groundwaters.

Electrochemical oxidation of benzothiophenes

1978 ◽  
Vol 43 (8) ◽  
pp. 2015-2023 ◽  
Author(s):  
Jan Šrogl ◽  
Miroslav Janda ◽  
Ivan Stibor ◽  
Jan Kos ◽  
Vlastimil Vyskočil
Keyword(s):  
Electrochemical Oxidation

Properties of electrochemically generated primary cationradicals of phenyl- and 2-(4-tolyl)-1,3,4,7-tetramethylisoindoles

1980 ◽  
Vol 45 (6) ◽  
pp. 1669-1676 ◽  
Author(s):  
Pavel Kubáček
Keyword(s):  
Electrochemical Oxidation ◽  
Spin Polarization ◽  
High Spin ◽  
Epr Spectroscopy ◽  
Half Life ◽  
Electrochemical Behaviour ◽  
Epr Spectra ◽  
Electrochemical Generation ◽  
Splitting Constant ◽  
Reduced Temperature

The first step of electrochemical oxidation of 2-phenyl- and 2-(4-tolyl)-1,3,4,7-tetramethylisoindoles in anhydrous acetonitrile produces relatively stable cationradicals which have been studied by means of EPR spectroscopy using the method of internal electrochemical generation of radicals under reduced temperature. The same electrochemical behaviour of the both studied derivatives and identical EPR spectra of their cationradicals can be explained within the Huckel MO method. The largest contribution to the magnitude of splitting constant of nitrogen nucleus is due to π-σ-spin polarization of C-N bonds caused by high spin abundance of pz-AO of carbon atoms. Half-life of decomposition of the studied cationradicals is 4 min at -30°C.

Anodic voltammetry of pyrazolone derivatives with the help of the self-cleaning rotating electrode

1987 ◽  
Vol 52 (1) ◽  
pp. 66-71 ◽  
Author(s):  
Vesselin C. Noninski ◽  
Emanuel B. Sobowale
Keyword(s):  
Electrochemical Oxidation ◽  
The Self ◽  
Good Reproducibility ◽  
Rotating Electrode ◽  
Pyrazolone Derivatives ◽  
Self Cleaning ◽  
Anodic Voltammetry

Nine pyrazolone derivatives have been studied by anodic voltammetry using gold self-cleaning rotating electrode (SRE). Voltamograms of good reproducibility are presented. On the basis of voltammetric data a mechanism is proposed for the electrochemical oxidation of sodium 1-phenyl-2,3-dimethyl-4-(N-methylamino)pyrazol-5-one-N-methansulphonate and 1-phenyl-2,3-dimethyl-4-(dimethylamino)pyrazol-5-one in protic medium.

Electroanalytical chemistry of vanadium complexes: Electrochemical oxidation of [V(IV)O(nta)(H2O)]-

1989 ◽  
Vol 54 (1) ◽  
pp. 64-69 ◽  
Author(s):  
Roland Meier ◽  
Gerhard Werner ◽  
Matthias Otto
Keyword(s):  
Cyclic Voltammetry ◽  
Electrochemical Oxidation ◽  
Ph Dependence ◽  
Differential Pulse ◽  
Nitrilotriacetic Acid ◽  
Reduced Form ◽  
Vanadium Complexes ◽  
Differential Pulse Polarography ◽  
Electroanalytical Chemistry ◽  
Ph Range

Electrochemical oxidation of [V(IV)O(nta)(H2O)]- (H3nta nitrilotriacetic acid) was studied in aqueous solution by means of cyclic voltammetry, differential pulse polarography, and current sampled DC polarography on mercury as electrode material. In the pH-range under study (5.5-9.0) the corresponding V(V) complex is produced by one-electron oxidation of the parent V(IV) species. The oxidation product is stable within the time scale of cyclic voltammetry. The evaluation of the pH-dependence of the half-wave potentials leads to a pKa value for [V(IV)O(nta)(H2O)]- which is in a good agreement with previous determinations. The measured value for E1/2 is very close to the formal potential E0 calculated via the Nernst equation on the basis of known literature values for log Kox and log Kred, the complex stability constants for the oxidized and reduced form, respectively.

Electrochemical Oxidation of Thiocyanate on Metal Oxide Electrodes

2019 ◽  
Vol 6 ◽  
pp. 219-226 ◽  
Author(s):  
O. Kosohin ◽  
O. Makohoniuk ◽  
A. Kushmyruk
Keyword(s):  
Metal Oxide ◽  
Electrochemical Oxidation ◽  
Oxide Electrodes
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