Comparing the Degradation Pathways of Hydrochlorothiazide and Sulfamethoxazole Using Ozone, Anodic Oxidation, and Electro-Fenton Processes

Read full text
Authors: Nadia Gadi, Rebecca Dhawle, Allisson Barros de Souza, Nadine C. Boelee, Deirdre Cabooter, Dionissios Mantzavinos, Raf Dewil
Cited by: 3
References: 61

Abstract

High Resolution Image Download MS PowerPoint Slide This study compared the performance of ozonation (O 3 ), anodic oxidation (AO), and electro-Fenton (EF) as advanced oxidation processes (AOPs) in the degradation and mineralization of two prevalent pharmaceutical pollutants: sulfamethoxazole (SMX) and hydrochlorothiazide (HCTZ). The effects of varying currents (150–500 mA) on AO and different Fe 2+ concentrations (0–42 mg L –1 ) on EF were examined. Both EF and O 3 achieved full removal of SMX and HCTZ, whereas AO resulted in 90% removal. EF demonstrated the highest mineralization efficiency, with 88% total organic carbon (TOC) removal, followed by AO at 74% and O 3 at 24%. Investigations into the degradation pathways of SMX and HCTZ under each AOP revealed identical degradation mechanisms for EF and AO, with hydroxyl ( • OH) radicals playing a crucial role. When tested on real municipal effluent, EF showed superior mineralization efficiency and was least affected by the water matrix. This study underscores the effectiveness of EF in the degradation and mineralization of pharmaceutical pollutants, presenting it as a viable option for large-scale wastewater treatment. This work provides the first side-by-side benchmark of O 3, AO, and the combined AO + EF process for a SMX/HCTZ mixture while jointly evaluating kinetics, TOC mineralization, transformation products, and real-effluent matrix effects.

Fields of Study & Subjects

Advanced oxidation water treatment Water Treatment and Disinfection Pharmaceutical and Antibiotic Environmental Impacts

Publication details

Journal / source
ACS ES&T Water
Publisher
American Chemical Society (ACS)
Volume
6
Issue
6
Pages
3328–3339
Publication date
11 May 2026
Language
EN