Multidimensional Analysis of Chlorine Photolysis for Astrazon Red 6B Degradation: Kinetics, Synergistic Effects, and Mechanistic Insights

ABSTRACT This study investigates the degradation of Astrazon Red 6B (AR 6B), a cationic textile dye, using the UV 254 /chlorine advanced oxidation process. A multidimensional experimental approach was employed to evaluate the process performance and synergy under varying operational conditions, including chlorine dosage (100–1000 μM), dye concentration (10 and 20 mg L −1 ), temperature (25°C–45°C), and pH (5, 7, and 9). Particular attention was given to pH, as it governs chlorine speciation and consequently the nature and reactivity of generated oxidative species. The combined UV/chlorine system exhibited significantly enhanced degradation compared to the individual processes (chlorination and UV irradiation), confirming a strong synergistic effect. By outperforming the UV/H 2 O 2 system, the highest performance (with a synergy index [SI] of 9.76) of the UV/chlorine system was observed under mildly acidic conditions (pH 5 with 250 μM chlorine, 20 mg L −1 dye, and 25°C), where reactive chlorine species (RCS) and hydroxyl radicals (the dominant oxidants) were simultaneously promoted, accelerating chromophore destruction and subsequent oxidative pathways. Neutral (pH 7) and alkaline (pH 9) conditions exhibited a different reactivity pattern, indicating a shift in the dominant radical species and reaction mechanisms. Variations in oxidant dose, pollutant concentration, and temperature further influenced the SI in a pH‐dependent manner, highlighting the complex interplay among radical generation, scavenging reactions, and substrate availability. Overall, the results demonstrate that the UV/chlorine process is a highly tunable oxidation system whose efficiency is strongly controlled by chlorine speciation and radical dynamics. The mechanistic insights provided contribute to a deeper understanding of reactive species interactions and support the optimization of UV/chlorine treatment for textile wastewater remediation.

Authors

Institutions

Publication Details

Journal
Water Environment Research
Published
2026-05-27
DOI
https://doi.org/10.1002/wer.70426
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Multidimensional Analysis of Chlorine Photolysis for Astrazon Red 6B Degradation: Kinetics, Synergistic Effects, and Mechanistic Insights

Aissa Dehane, Chawki Djelloul, Oualid Hamdaoui, Slimane Merouani et al.
Water Environment Research
Advanced oxidation water treatment
article

Multidimensional Analysis of Chlorine Photolysis for Astrazon Red 6B Degradation: Kinetics, Synergistic Effects, and Mechanistic Insights

Aissa Dehane, Chawki Djelloul, Oualid Hamdaoui, Slimane Merouani, Mounia Tidjani
article en

Abstract

ABSTRACT This study investigates the degradation of Astrazon Red 6B (AR 6B), a cationic textile dye, using the UV 254 /chlorine advanced oxidation process. A multidimensional experimental approach was employed to evaluate the process performance and synergy under varying operational conditions, including chlorine dosage (100–1000 μM), dye concentration (10 and 20 mg L −1 ), temperature (25°C–45°C), and pH (5, 7, and 9). Particular attention was given to pH, as it governs chlorine speciation and consequently the nature and reactivity of generated oxidative species. The combined UV/chlorine system exhibited significantly enhanced degradation compared to the individual processes (chlorination and UV irradiation), confirming a strong synergistic effect. By outperforming the UV/H 2 O 2 system, the highest performance (with a synergy index [SI] of 9.76) of the UV/chlorine system was observed under mildly acidic conditions (pH 5 with 250 μM chlorine, 20 mg L −1 dye, and 25°C), where reactive chlorine species (RCS) and hydroxyl radicals (the dominant oxidants) were simultaneously promoted, accelerating chromophore destruction and subsequent oxidative pathways. Neutral (pH 7) and alkaline (pH 9) conditions exhibited a different reactivity pattern, indicating a shift in the dominant radical species and reaction mechanisms. Variations in oxidant dose, pollutant concentration, and temperature further influenced the SI in a pH‐dependent manner, highlighting the complex interplay among radical generation, scavenging reactions, and substrate availability. Overall, the results demonstrate that the UV/chlorine process is a highly tunable oxidation system whose efficiency is strongly controlled by chlorine speciation and radical dynamics. The mechanistic insights provided contribute to a deeper understanding of reactive species interactions and support the optimization of UV/chlorine treatment for textile wastewater remediation.

Water Environment ResearchVol. 98(6)
University Frères Mentouri Constantine 1 (DZ), University of Algiers Benyoucef Benkhedda (DZ), King Saud University (SA), Université Constantine 2 (DZ)
Clean water and sanitation
Openalex Percentile: Top 11%
Advanced oxidation water treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.