Electrochemical oxidation of four pharmaceutical pollutants using Ti/IrO2 and Nb/BDD anodes: Application of factorial design methodology

The simultaneous oxidation of four PhCs (Carbamazepine (CBZ), Caffeine (CAF), Ibuprofen (IBU), and Diclofenac (DFC)) has been investigated by electrochemical oxidation process using Ti/IrO 2 and Nb/BDD anode electrodes, respectively. The initial concentration of each PhCs was 69 µg/L. The effectiveness of the electro-oxidation process was due to its capability of oxidizing PhCs at the anode surface and in solution. A factorial experimental design was used for determining the influent parameters on the PhCs degradation. Four factors were investigated: supporting electrolyte concentration, current density, period of electrolysis and anode type. Anode type and treatment time were the most influent parameters on the electrochemical degradation of pollutants. By using a 2 4 factorial design, the best performance for PhCs degradation (more than 99 % of each PhC removed) was obtained by using boron doped diamond anode electrode (BDD) operated at a current density of 5.24 mA/cm 2 during 70 min of period treatment time in the presence of 1.0 g Na 2 SO 4 /L. However, the period of treatment time could be five times reduced (to simultaneously remove around 100 % of each PhC) while using NaCl as supporting electrolyte (instead of Na 2 SO 4 ). This was mainly attributed to the combination of direct and indirect effect of electrolysis, more effective in the case of NaCl used as supporting electrolyte compared to Na 2 SO 4 . The direct effect of electrolysis contributed to oxidize 40–80 % of PhCs (namely for DFC, IBU and CAF), whereas more than 99 % of CBZ could be oxidized owing to the sole direct effect of electrolysis. • FD was used to study electro-oxidation of four PhCs (CBZ, CAF, IBU and DFC). • Anode and current intensity were the main parameters influencing PhCs degradation. • BDD anode material was more effective than Ti/IrO 2 operated at 5.24 mA/cm 2 . • More than 99 % of PhC was removed using Na 2 SO 4 as electrolyte for 70 min period • Treatment time was five times reduced while using NaCl compared to Na 2 SO 4

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Publication Details

Journal
International Journal of Electrochemical Science
Published
2025-10-18
DOI
https://doi.org/10.1016/j.ijoes.2025.101211
Citations
2
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
1.63
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article

Electrochemical oxidation of four pharmaceutical pollutants using Ti/IrO2 and Nb/BDD anodes: Application of factorial design methodology

Patrick Drogui, Bi Gouessé Henri Briton, Yao Kouassi Benjamin, Akotto Achiepo Gaetan et al.
2 citations
International Journal of Electrochemical Science
Advanced oxidation water treatment
1.63
article

Electrochemical oxidation of four pharmaceutical pollutants using Ti/IrO2 and Nb/BDD anodes: Application of factorial design methodology

Patrick Drogui, Bi Gouessé Henri Briton, Yao Kouassi Benjamin, Akotto Achiepo Gaetan, Ngoma Tsaty Veronique
article en
2 citations

Abstract

The simultaneous oxidation of four PhCs (Carbamazepine (CBZ), Caffeine (CAF), Ibuprofen (IBU), and Diclofenac (DFC)) has been investigated by electrochemical oxidation process using Ti/IrO 2 and Nb/BDD anode electrodes, respectively. The initial concentration of each PhCs was 69 µg/L. The effectiveness of the electro-oxidation process was due to its capability of oxidizing PhCs at the anode surface and in solution. A factorial experimental design was used for determining the influent parameters on the PhCs degradation. Four factors were investigated: supporting electrolyte concentration, current density, period of electrolysis and anode type. Anode type and treatment time were the most influent parameters on the electrochemical degradation of pollutants. By using a 2 4 factorial design, the best performance for PhCs degradation (more than 99 % of each PhC removed) was obtained by using boron doped diamond anode electrode (BDD) operated at a current density of 5.24 mA/cm 2 during 70 min of period treatment time in the presence of 1.0 g Na 2 SO 4 /L. However, the period of treatment time could be five times reduced (to simultaneously remove around 100 % of each PhC) while using NaCl as supporting electrolyte (instead of Na 2 SO 4 ). This was mainly attributed to the combination of direct and indirect effect of electrolysis, more effective in the case of NaCl used as supporting electrolyte compared to Na 2 SO 4 . The direct effect of electrolysis contributed to oxidize 40–80 % of PhCs (namely for DFC, IBU and CAF), whereas more than 99 % of CBZ could be oxidized owing to the sole direct effect of electrolysis. • FD was used to study electro-oxidation of four PhCs (CBZ, CAF, IBU and DFC). • Anode and current intensity were the main parameters influencing PhCs degradation. • BDD anode material was more effective than Ti/IrO 2 operated at 5.24 mA/cm 2 . • More than 99 % of PhC was removed using Na 2 SO 4 as electrolyte for 70 min period • Treatment time was five times reduced while using NaCl compared to Na 2 SO 4

International Journal of Electrochemical ScienceVol. 20(12)
Institut National de la Recherche Scientifique (CA), Institut National Polytechnique Félix Houphouët-Boigny (CI), Réseau Technoscience (CA)
Openalex Percentile: Top 14%
Advanced oxidation water treatment
1.63
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