Catalytic Degradation of Sulfamethazine by Ferrate(VI)-Activated Calcium Sulfite: Performance and Mechanism
- 1Environment Monitoring Center of Jiangsu Province, Nanjing 210019, China
- 2Nanjing Shenghong Environmental Technology Co., Ltd., Nanjing 210017, China
- 3College of Ecology and Environment, Nanjing Forestry University, Nanjing 210037, China
Abstract
Calcium sulfite (CaSO3) is introduced as a solid-phase sulfite source with slow-release characteristics to overcome the drawbacks of highly soluble sulfite in conventional S(IV)-based advanced oxidation processes (AOPs). In this work, we establish a catalytic Fe(VI)/CaSO3 system for the efficient degradation of sulfamethazine (SMT). The system operates through a catalytic cycle wherein ferrate(VI) activates sulfite to generate sulfate radicals (SO4•−) and hydroxyl radicals (•OH) as the primary reactive oxygen species (ROS), with concomitant involvement of high-valent iron species (Fe(V)/Fe(IV)) and singlet oxygen (1O2). The catalytic mechanism, involving electron transfer and radical chain reactions, is elucidated by EPR spectroscopy, radical quenching experiments, and probe tests. The Fe(VI)/CaSO3 system achieves 98.6% SMT removal within 20 min and exhibits broad-spectrum activity against various organic pollutants. The catalytic performance remains robust over a wide pH range and in the presence of coexisting ions and natural organic matter. This study highlights the potential of ferrate(VI)-activated calcium sulfite as a promising catalytic AOP platform for water treatment.
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BibTeX
@article{fu2026catalytic,
title = {{Catalytic Degradation of Sulfamethazine by Ferrate(VI)-Activated Calcium Sulfite: Performance and Mechanism}},
author = {Dan Fu and Yonggang Zhao and Honglei Liu and Mo Peng and Yuwei Pan},
journal = {Catalysts},
year = {2026},
month = nov,
doi = {10.3390/catal16110979},
url = {https://www.mdpi.com/2073-4344/16/11/979},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - Catalytic Degradation of Sulfamethazine by Ferrate(VI)-Activated Calcium Sulfite: Performance and Mechanism
AU - Dan Fu
AU - Yonggang Zhao
AU - Honglei Liu
AU - Mo Peng
AU - Yuwei Pan
PY - 2026
DA - 2026/11/02
JO - Catalysts
DO - 10.3390/catal16110979
UR - https://www.mdpi.com/2073-4344/16/11/979
AB - Calcium sulfite (CaSO3) is introduced as a solid-phase sulfite source with slow-release characteristics to overcome the drawbacks of highly soluble sulfite in conventional S(IV)-based advanced oxidation processes (AOPs). In this work, we establish a catalytic Fe(VI)/CaSO3 system for the efficient degradation of sulfamethazine (SMT). The system operates through a catalytic cycle wherein ferrate(VI) activates sulfite to generate sulfate radicals (SO4•−) and hydroxyl radicals (•OH) as the primary reactive oxygen species (ROS), with concomitant involvement of high-valent iron species (Fe(V)/Fe(IV)) and singlet oxygen (1O2). The catalytic mechanism, involving electron transfer and radical chain reactions, is elucidated by EPR spectroscopy, radical quenching experiments, and probe tests. The Fe(VI)/CaSO3 system achieves 98.6% SMT removal within 20 min and exhibits broad-spectrum activity against various organic pollutants. The catalytic performance remains robust over a wide pH range and in the presence of coexisting ions and natural organic matter. This study highlights the potential of ferrate(VI)-activated calcium sulfite as a promising catalytic AOP platform for water treatment.
SN - 2073-4344
ER -