Insight in sulfadiazine degradation by peroxymonosulfate activated by polydopamine-derived nitrogen-doped carbon supported CoFe2O4: Co leaching inhibition and degradation enhancement

Heterogeneous catalyst-mediated sulfate radical-based advanced oxidation processes (SR-AOPs) showed excellent performance during antibiotics degradation. Spinel was a promising catalyst for SR-AOPs, but the secondary contamination due to metal ions leaching needed to be addressed. And the destruction of catalyst structure could lead to the reduction of catalytic activity and the difficulty of recovery. Thus, a novel nitrogen-doped carbon (NC)-supported CoFe<sub>2</sub>O<sub>4</sub> (CoFe<sub>2</sub>O<sub>4</sub>@NC) was synthesized as the activator of PMS for sulfadiazine (SDZ) degradation under low Co leaching conditions. The consequences indicated that the CoFe<sub>2</sub>O<sub>4</sub>@NC/PMS system exhibited higher PMS decomposition efficiency and reaction stoichiometry efficiency than the bare CoFe<sub>2</sub>O<sub>4</sub>/PMS systems (CoFe<sub>2</sub>O<sub>4</sub>-180 and CoFe<sub>2</sub>O<sub>4</sub>-800), which in turn demonstrated a better SDZ removal performance. Under the condition of CoFe<sub>2</sub>O<sub>4</sub>@NC dosage 0.1 g/L, PMS concentration 0.5 mM, solution pH 6.8 and temperature 25°C, SDZ (20 mg/L) was almost completely degraded within 60 min. XPS analysis showed that the NC not only protected and stabilized CoFe<sub>2</sub>O<sub>4</sub>, but also provided additional active sites for PMS activation. During SDZ degradation, SO<sub>4</sub><sup>•-</sup>, HO<sup>•</sup>, <sup>•</sup>O<sub>2</sub><sup>-</sup> and <sup>1</sup>O<sub>2</sub> were involved in the reaction, among which SO<sub>4</sub><sup>•</sup> and HO<sup>•</sup> made the main contribution. Meanwhile, CoFe<sub>2</sub>O<sub>4</sub>@NC could be recovered by magnetic separation, and showed great stability (Co leaching 0.852 mg/L) and reusability. In the fifth cycle experiment, 85.02 % SDZ degradation was obtained. Based on the detected intermediates (12 intermediates were identified) and DFT calculations, possible degradation pathways for SDZ in CoFe<sub>2</sub>O<sub>4</sub>@NC/PMS were proposed. The condensed dual descriptor indicated that the N7, N11, and C15 atoms on SDZ molecule were the main sites of electrophilic attack, which was consistent with the detected intermediates. The degradation of SDZ involved hydroxylation of NH<sub>2</sub>, cleavage of S-N and extrusion of SO<sub>2</sub>. This study explored the improvements made in NC support material to catalytic performance and resistance to dissolution of spinel, providing new insights for subsequent researches.

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Publication Details

Journal
Ecotoxicology and Environmental Safety
Published
2024-10-01
DOI
https://doi.org/10.1016/j.ecoenv.2024.117126
Citations
12
Primary Topic
Advanced oxidation water treatment
Type
article
Field-Weighted Citation Impact
2.42
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article

Insight in sulfadiazine degradation by peroxymonosulfate activated by polydopamine-derived nitrogen-doped carbon supported CoFe2O4: Co leaching inhibition and degradation enhancement

Li Huang, Ziyi Chen, Sirui Li, Junyuan Guo et al.
12 citations
Ecotoxicology and Environmental Safety
Advanced oxidation water treatment
2.42
article

Insight in sulfadiazine degradation by peroxymonosulfate activated by polydopamine-derived nitrogen-doped carbon supported CoFe2O4: Co leaching inhibition and degradation enhancement

Li Huang, Ziyi Chen, Sirui Li, Junyuan Guo, Ling Pu
article en
12 citations

Abstract

Heterogeneous catalyst-mediated sulfate radical-based advanced oxidation processes (SR-AOPs) showed excellent performance during antibiotics degradation. Spinel was a promising catalyst for SR-AOPs, but the secondary contamination due to metal ions leaching needed to be addressed. And the destruction of catalyst structure could lead to the reduction of catalytic activity and the difficulty of recovery. Thus, a novel nitrogen-doped carbon (NC)-supported CoFe<sub>2</sub>O<sub>4</sub> (CoFe<sub>2</sub>O<sub>4</sub>@NC) was synthesized as the activator of PMS for sulfadiazine (SDZ) degradation under low Co leaching conditions. The consequences indicated that the CoFe<sub>2</sub>O<sub>4</sub>@NC/PMS system exhibited higher PMS decomposition efficiency and reaction stoichiometry efficiency than the bare CoFe<sub>2</sub>O<sub>4</sub>/PMS systems (CoFe<sub>2</sub>O<sub>4</sub>-180 and CoFe<sub>2</sub>O<sub>4</sub>-800), which in turn demonstrated a better SDZ removal performance. Under the condition of CoFe<sub>2</sub>O<sub>4</sub>@NC dosage 0.1 g/L, PMS concentration 0.5 mM, solution pH 6.8 and temperature 25°C, SDZ (20 mg/L) was almost completely degraded within 60 min. XPS analysis showed that the NC not only protected and stabilized CoFe<sub>2</sub>O<sub>4</sub>, but also provided additional active sites for PMS activation. During SDZ degradation, SO<sub>4</sub><sup>•-</sup>, HO<sup>•</sup>, <sup>•</sup>O<sub>2</sub><sup>-</sup> and <sup>1</sup>O<sub>2</sub> were involved in the reaction, among which SO<sub>4</sub><sup>•</sup> and HO<sup>•</sup> made the main contribution. Meanwhile, CoFe<sub>2</sub>O<sub>4</sub>@NC could be recovered by magnetic separation, and showed great stability (Co leaching 0.852 mg/L) and reusability. In the fifth cycle experiment, 85.02 % SDZ degradation was obtained. Based on the detected intermediates (12 intermediates were identified) and DFT calculations, possible degradation pathways for SDZ in CoFe<sub>2</sub>O<sub>4</sub>@NC/PMS were proposed. The condensed dual descriptor indicated that the N7, N11, and C15 atoms on SDZ molecule were the main sites of electrophilic attack, which was consistent with the detected intermediates. The degradation of SDZ involved hydroxylation of NH<sub>2</sub>, cleavage of S-N and extrusion of SO<sub>2</sub>. This study explored the improvements made in NC support material to catalytic performance and resistance to dissolution of spinel, providing new insights for subsequent researches.

Ecotoxicology and Environmental SafetyVol. 285
Chengdu University of Information Technology (CN), Sichuan Academy Of Social Sciences (CN), Sichuan Academy of Agricultural Sciences (CN)
Openalex Percentile: Top 12%
Advanced oxidation water treatment
2.42
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