Degradation of organic pollutants in natural magnetite-activated peroxymonosulfate system enhanced by hydroxylamine: Catalytic performance, reaction pathway, and enhancement mechanism

The degradation of organic pollutants using natural minerals in advanced oxidation process gains increasing interest due to abundant resources, rich active metals, and easy engineered preparation, but it is limited by the relatively low catalytic performance of natural minerals. The enhanced pollutant degradation in natural mineral/peroxymonosulfate (PMS) system has been rarely studied. In this work, the enhancement of hydroxylamine natural magnetite/PMS system was innovatively proposed. In comparison with the natural magnetite/PMS system, the degradation efficiency of Rhodamine B (RhB) was increased by 61.82 % after the addition of hydroxylamine, and the RhB degradation followed a pseudo-first-order kinetic model with a rate constant of 0.1040 min −1 . The Fe 2+ /Fe 3+ conversion efficiency was improved by the synergistic effect of hydroxylamine, which was demonstrated by X-ray photoelectron spectroscopy and determination of the Fe 2+ concentration in the reaction system. The influence of process factors on the degradation process was examined, including hydroxylamine concentration, catalyst dosage, PMS concentration, initial pH, temperature, inorganic anions, and humic acid. The hydroxylamine-assisted natural magnetite/PMS system exhibited a wider pH range (3−11) and good reusability (degradation efficiency of 90.30 % for the seventh run). Besides, the effective degradation of different organic pollutants was obtained, including methyl organic, malachite green, tetracycline, sulfadiazine, and ofloxacin. Sulfate radical, hydroxyl radical, and singlet oxygen were mainly reactive oxygen species in the reaction system. The energy consumption was only 4.33 kWh/kg, significantly lower than previously reported systems, showing a significant environmental application value. • The roles of hydroxylamine in natural magnetite/PMS system are examined. • Hydroxylamine increases RhB degradation by 61.82 % in the catalytic system. • Reactive species of SO4·-, ·OH, 1O2 is involved in pollutant degradation. • Natural magnetite is effective in wide pH range (3–11) and has good reusability.

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Publication Details

Journal
Journal of Water Process Engineering
Published
2024-08-23
DOI
https://doi.org/10.1016/j.jwpe.2024.106000
Citations
18
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
3.63
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article

Degradation of organic pollutants in natural magnetite-activated peroxymonosulfate system enhanced by hydroxylamine: Catalytic performance, reaction pathway, and enhancement mechanism

Hong‐Wen Liu, Kai Jia, Chongqing Wang, Xingyang Li et al.
18 citations
Journal of Water Process Engineering
Advanced oxidation water treatment
3.63
article

Degradation of organic pollutants in natural magnetite-activated peroxymonosulfate system enhanced by hydroxylamine: Catalytic performance, reaction pathway, and enhancement mechanism

Hong‐Wen Liu, Kai Jia, Chongqing Wang, Xingyang Li, Yijun Cao
article en
18 citations

Abstract

The degradation of organic pollutants using natural minerals in advanced oxidation process gains increasing interest due to abundant resources, rich active metals, and easy engineered preparation, but it is limited by the relatively low catalytic performance of natural minerals. The enhanced pollutant degradation in natural mineral/peroxymonosulfate (PMS) system has been rarely studied. In this work, the enhancement of hydroxylamine natural magnetite/PMS system was innovatively proposed. In comparison with the natural magnetite/PMS system, the degradation efficiency of Rhodamine B (RhB) was increased by 61.82 % after the addition of hydroxylamine, and the RhB degradation followed a pseudo-first-order kinetic model with a rate constant of 0.1040 min −1 . The Fe 2+ /Fe 3+ conversion efficiency was improved by the synergistic effect of hydroxylamine, which was demonstrated by X-ray photoelectron spectroscopy and determination of the Fe 2+ concentration in the reaction system. The influence of process factors on the degradation process was examined, including hydroxylamine concentration, catalyst dosage, PMS concentration, initial pH, temperature, inorganic anions, and humic acid. The hydroxylamine-assisted natural magnetite/PMS system exhibited a wider pH range (3−11) and good reusability (degradation efficiency of 90.30 % for the seventh run). Besides, the effective degradation of different organic pollutants was obtained, including methyl organic, malachite green, tetracycline, sulfadiazine, and ofloxacin. Sulfate radical, hydroxyl radical, and singlet oxygen were mainly reactive oxygen species in the reaction system. The energy consumption was only 4.33 kWh/kg, significantly lower than previously reported systems, showing a significant environmental application value. • The roles of hydroxylamine in natural magnetite/PMS system are examined. • Hydroxylamine increases RhB degradation by 61.82 % in the catalytic system. • Reactive species of SO4·-, ·OH, 1O2 is involved in pollutant degradation. • Natural magnetite is effective in wide pH range (3–11) and has good reusability.

Journal of Water Process EngineeringVol. 66
Zhengzhou University (CN)
Openalex Percentile: Top 7%
Advanced oxidation water treatment
3.63
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