Magnetic Fe-doped silicon carbide induced microwave activated persulfate for decabromodiphenyl ether removal: Mechanism and unique degradation pathway

In this work, the magnetic nanocomposite Fe@SiC was prepared by a hydrothermal method and determined by SEM, XRD, XPS, FTIR and VNA. Fe3O4 particles were loaded onto SiC with great success, and the synthesized composites had favorable microwave absorption properties. Fe@SiC was used to activate pers...

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Veröffentlicht in:Chemosphere (Oxford) 2024-02, Vol.349, p.140841-140841, Article 140841
Hauptverfasser: Liu, Yuxin, Lin, Qintie, Zheng, Junli, Fan, Xindan, Xu, Kehuan, Ma, Yongjie, He, Jin
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Sprache:eng
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Zusammenfassung:In this work, the magnetic nanocomposite Fe@SiC was prepared by a hydrothermal method and determined by SEM, XRD, XPS, FTIR and VNA. Fe3O4 particles were loaded onto SiC with great success, and the synthesized composites had favorable microwave absorption properties. Fe@SiC was used to activate persulfate in a microwave field for the degradation of BDE209 in soil. Specifically, the synergistic interaction between microwaves and Fe@SiC showed excellent catalytic performance in activating PS to degrade BDE209 (90.1% BDE209 degradation in 15 min). The presence of •OH, O2•− and 1O2 was demonstrated based on quench trapping and EPR experiments. LC‒MS was applied to determine the intermediates and propose the possible degradation pathway for BDE209 in the MW/Fe@SiC/PS system, and it was found that BDE209 produced almost no lower brominated diphenyl ethers. Therefore, the toxicity of BDE209 was found to be reduced using toxicity assessment software. Overall, this work provides an effective approach for the degradation of BDE209 in environmental remediation. [Display omitted] •The degradation and debromination of BDE209 in soil was significantly enhanced.•Fe@SiC has excellent microwave absorption properties.•1O2, O2.•− and •OH were identified as active substances in the reaction.•Almost no highly toxic low bromo-diphenyl ethers were produced.
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2023.140841