Exploring the electro-oxidation of the iodinated contrast iopamidol on different electrode materials for wastewater treatment

• Si/BDD, Ti/Pt and Pt-doped Ti/SnO 2 -Sb anodes can oxidize and mineralize IOPA. • Oxidation efficiencies greater than 80 % were found for all anodes in 3 h experiments. • Electro-oxidation of IOPA avoids generation of toxic iodine-containing intermediates. • Si/BDD is the most efficient anode towards IOPA abatement. • Ti/SnO 2 -Sb-Pt is proposed as cheaper alternative to treat iodinated contrast media. Emerging contaminants in water pose a serious threat to the environment and human health, stressing the need of developing efficient treatment processes. In this work, the electrochemical degradation of iopamidol (IOPA), as model iodinated organic pollutant, and the formation of its by-products were investigated on different electrode materials, including commercial anodes (Ti/Pt and Si/BDD) and a synthetized Ti/SnO 2 -Sb-Pt(13 %) electrode. The electrochemical behaviour and catalytic activity were studied in Na 2 SO 4 by cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic experiments in a filter-press reactor. The results show that IOPA can be effectively degraded with all the studied anodes by anodic treatment, involving both the direct and OHs-mediated oxidation routes. The degradation efficiency achieved after 3 h of electrolysis was found greater than 80 % for all electrodes, being Si/BDD the most efficient anode. By-products analyses with HPLC/MS and ionic chromatography demonstrate the selective dehalogenation of IOPA as the main reaction pathway, giving rise to the formation of non-toxic deiodinated organic compounds. The unselective and highly oxidizing capability of Si/BDD results in rapid and complete mineralization but promotes the accumulation of toxic oxidants and most oxidized inorganic products in the treated residue. By contrast, the lower but more controllable oxidative conditions associated to Pt-containing electrodes enable the conversion of pollutants into valuable compounds and the production of non-toxic aqueous residues. The promoted IOPA interaction and OHs generation induced by Pt and the SnO 2 -Sb matrix, respectively, observed for Ti/SnO 2 -Sb-Pt(13 %), together with its comparatively lower cost, make this anode a good candidate to revalorize or eliminate iodinated organic contrast media.

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Publication Details

Journal
Separation and Purification Technology
Published
2025-04-05
DOI
https://doi.org/10.1016/j.seppur.2025.132860
Citations
3
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
2.45
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article

Exploring the electro-oxidation of the iodinated contrast iopamidol on different electrode materials for wastewater treatment

Emilia Morallón, Andrés Felipe Quintero-Jaime, R. Berenguer, Sara J. González
3 citations
Separation and Purification Technology
Advanced oxidation water treatment
2.45
article

Exploring the electro-oxidation of the iodinated contrast iopamidol on different electrode materials for wastewater treatment

Emilia Morallón, Andrés Felipe Quintero-Jaime, R. Berenguer, Sara J. González
article en
3 citations

Abstract

• Si/BDD, Ti/Pt and Pt-doped Ti/SnO 2 -Sb anodes can oxidize and mineralize IOPA. • Oxidation efficiencies greater than 80 % were found for all anodes in 3 h experiments. • Electro-oxidation of IOPA avoids generation of toxic iodine-containing intermediates. • Si/BDD is the most efficient anode towards IOPA abatement. • Ti/SnO 2 -Sb-Pt is proposed as cheaper alternative to treat iodinated contrast media. Emerging contaminants in water pose a serious threat to the environment and human health, stressing the need of developing efficient treatment processes. In this work, the electrochemical degradation of iopamidol (IOPA), as model iodinated organic pollutant, and the formation of its by-products were investigated on different electrode materials, including commercial anodes (Ti/Pt and Si/BDD) and a synthetized Ti/SnO 2 -Sb-Pt(13 %) electrode. The electrochemical behaviour and catalytic activity were studied in Na 2 SO 4 by cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic experiments in a filter-press reactor. The results show that IOPA can be effectively degraded with all the studied anodes by anodic treatment, involving both the direct and OHs-mediated oxidation routes. The degradation efficiency achieved after 3 h of electrolysis was found greater than 80 % for all electrodes, being Si/BDD the most efficient anode. By-products analyses with HPLC/MS and ionic chromatography demonstrate the selective dehalogenation of IOPA as the main reaction pathway, giving rise to the formation of non-toxic deiodinated organic compounds. The unselective and highly oxidizing capability of Si/BDD results in rapid and complete mineralization but promotes the accumulation of toxic oxidants and most oxidized inorganic products in the treated residue. By contrast, the lower but more controllable oxidative conditions associated to Pt-containing electrodes enable the conversion of pollutants into valuable compounds and the production of non-toxic aqueous residues. The promoted IOPA interaction and OHs generation induced by Pt and the SnO 2 -Sb matrix, respectively, observed for Ti/SnO 2 -Sb-Pt(13 %), together with its comparatively lower cost, make this anode a good candidate to revalorize or eliminate iodinated organic contrast media.

Separation and Purification TechnologyVol. 367
University of Alicante (ES)
Clean water and sanitation
Openalex Percentile: Top 12%
Advanced oxidation water treatment
2.45
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