PMID- 38307338 OWN - NLM STAT- MEDLINE DCOM- 20240311 LR - 20240311 IS - 1879-1298 (Electronic) IS - 0045-6535 (Linking) VI - 352 DP - 2024 Mar TI - Characterization and electrochemical properties of TiO(2)-rNTs/SnO(2)-Sb/PbO(2) electrodes for the mineralization of persistent organic pollutants using anodic oxidation coupled Electro-Fenton treatment: Effect of precursor selection. PG - 141307 LID - S0045-6535(24)00200-5 [pii] LID - 10.1016/j.chemosphere.2024.141307 [doi] AB - The present study compares the effect of using different solvents on the electrochemical properties of the reduced TiO(2) nanotubes (TiO(2)-rNTs) layered Ti/TiO(2)-rNTs/SnO(2)-Sb/PbO(2) anodes. The electrodes are prepared using three different solvent-based precursors: (i) isopropanol, (ii) ethylene glycol and citric acid (Pechini method), and (iii) 2-hydroxyethylammonium acetate (2HEAA) ionic liquid (IL) via the thermal decomposition route. The decomposition mechanism of precursor solutions was explored using the thermogravimetric (TGA) analysis. Further, the physicochemical properties of the electrodes are examined using Field emission Scanning Electron microscopy (FE-SEM), X-ray diffraction spectroscopy (XRD), and X-ray photoelectron emission spectroscopy (XPS). The results revealed that solvents with higher viscosity and slower decomposition rates support better film uniformity and higher stability of the electrode. The TiO(2) -rNTs bottom layer and PbO(2) top layer helped obtain higher film stability, increased working potential window (2.2 V vs. SHE) of the electrode, and the repeatability of the results. The performance of different electrodes based on the precursor solution is found as IL >> Pechini > Isopropanol. 4-chlorophenol (4-CP) is used as a model pollutant to test the performance of IL-Ti/TiO(2)-rNTs/SnO(2)-Sb/PbO(2) anode in an anodic oxidation (AO) coupled electro-Fenton (EF) treatment. Further, the reliability of the electrode is evaluated by mineralizing other persistent organic pollutants (POPs) like tetracyclin, phenol, 2-chlorophenol (2-CP), and 2,4-dichlorophenol (2,4-DCP). Under the optimized conditions, the proposed system was able to mineralize the tetracyclin, phenol, 2-CP, 2,4-DCP, and 4-CP up to 78.91, 82.07, 74.96, 78.78, and 69.3 %, respectively. Moreover, the degradation mechanism of chlorophenols is proposed. CI - Copyright (c) 2024 Elsevier Ltd. All rights reserved. FAU - Rai, Devendra AU - Rai D AD - Department of Chemical Engineering, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India. Electronic address: drai@ch.iitr.ac.in. FAU - Sinha, Shishir AU - Sinha S AD - Department of Chemical Engineering, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand, 247667, India. Electronic address: shishir@ch.iitr.ac.in. LA - eng PT - Journal Article DEP - 20240131 PL - England TA - Chemosphere JT - Chemosphere JID - 0320657 RN - 0 (Oxides) RN - 0 (Persistent Organic Pollutants) RN - ND2M416302 (2-Propanol) RN - D1JT611TNE (Titanium) RN - 0 (Phenols) RN - 339NCG44TV (Phenol) RN - 0 (Solvents) RN - 0 (Water Pollutants, Chemical) SB - IM MH - *Oxides/chemistry MH - Persistent Organic Pollutants MH - 2-Propanol MH - Reproducibility of Results MH - Titanium/chemistry MH - Oxidation-Reduction MH - Phenols MH - Phenol/chemistry MH - Electrodes MH - Solvents MH - *Water Pollutants, Chemical/chemistry OTO - NOTNLM OT - Chlorophenol OT - EAOPs OT - Electro-Fenton OT - Ionic liquid OT - Reduced TiO(2) nanotubes OT - Ti/SnO(2)-Sb/PbO(2) anode COIS- Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. EDAT- 2024/02/03 00:42 MHDA- 2024/03/11 06:42 CRDT- 2024/02/02 19:31 PHST- 2023/09/26 00:00 [received] PHST- 2024/01/23 00:00 [revised] PHST- 2024/01/25 00:00 [accepted] PHST- 2024/03/11 06:42 [medline] PHST- 2024/02/03 00:42 [pubmed] PHST- 2024/02/02 19:31 [entrez] AID - S0045-6535(24)00200-5 [pii] AID - 10.1016/j.chemosphere.2024.141307 [doi] PST - ppublish SO - Chemosphere. 2024 Mar;352:141307. doi: 10.1016/j.chemosphere.2024.141307. Epub 2024 Jan 31.