Abstract
ZnFe-layered double oxides@biochar (ZnFe-LDO@BC) was constructed by in situ derivation of the ZnFe-LDH on biochar (BC) through a simple co-pyrolysis method for heterogeneous catalytic ozonation (HCO) progress. The dual-engine driven interface adsorption-catalysis of ozone (O3) on ZnFe-LDO@BC achieved durable organic water decontamination. The O3/ZnFe-LDO@BC system enhanced the utilization of O3 and the yield of hydroxyl radicals (·OH), thus greatly benefiting organic pollutants removal. Moreover, the enrichment of O3 and pollutants at the ZnFe-LDO@BC interface overcame the interpretation of the coexistence component, and showed unique advantages compared to traditional catalytic systems. In situ ATR-FTIR experiment and computational studies unveiled that the in situ formed Fe sites on LDO readily adsorbed H2O to form surface -OH and thus reacted with adsorbed O3, and mediated the ·OH dominant HCO process. The O3/ZnFe-LDO@BC system induced non-toxic degradation of pollutants. The constructed interfacial adsorption-catalysis system proposed a new ideal for the development of HCO technology, and provided a solution approach for technical bottlenecks.
| Original language | English |
|---|---|
| Article number | 135358 |
| Journal | Separation and Purification Technology |
| Volume | 380 |
| DOIs | |
| State | Published - 7 Feb 2026 |
| Externally published | Yes |
Keywords
- Catalytic ozonation
- DFT calculation
- Interfacial adsorption-catalysis
- Underlying mechanism
- ZnFe-LDO@BC
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