Bimetallic (Cu, Zn) ZIF-derived S-scheme heterojunction for efficient remediation of aqueous pollutants in visible light/peroxymonosulfate system
The design of suitable catalyst is the bottleneck in the photo-assisted Fenton-like reaction system. Here we constructed a S-scheme heterojunction consisted of CuO and Cu doped ZnO using Cu-ZIF-8 as precursor. The as-prepared composite catalyst possesses outstanding catalytic activation performance...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2023-08, Vol.330, p.122539, Article 122539 |
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Sprache: | eng |
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Zusammenfassung: | The design of suitable catalyst is the bottleneck in the photo-assisted Fenton-like reaction system. Here we constructed a S-scheme heterojunction consisted of CuO and Cu doped ZnO using Cu-ZIF-8 as precursor. The as-prepared composite catalyst possesses outstanding catalytic activation performance and broad-spectrum degradation capacity. To clearly fit and describe the overall reaction, a pseudo-third-order kinetic model was developed based on the second-order peroxymonosulfate (PMS) consumption and first-order methylene blue removal. The catalyst/visible light/ PMS composite reaction system provides remarkable mineralization and anti-interference ability, and is environmental friendliness. The interaction of Cu/Zn bimetallic sites realized the effective utilization of PMS, accelerated the PMS activation and promoted the formation of the highly oxidative SO5•−. Overall, this work provides new systematic insights on PMS activation by Cu/Zn bimetallic oxide S-scheme heterojunction and is of significance for sewage purification.
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•A S-scheme heterojunction was constructed by using Cu-ZIF-8 as precursor.•The as-prepared CuZnO-3 exhibited superior catalytic activation capability.•A pseudo-third-order kinetic model was developed involving the reacted MB and PMS.•The CuZnO-3/vis/PMS reaction system was evaluated to be environmentally friendly.•The catalytic activation mechanism of Cu/Zn bimetallic sites was proposed. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2023.122539 |