Abstract
Harmful algae pollution in eutrophic waters represents one of the most serious problems in natural water environment. Adsorption assisted photocatalytic inactivation is often considered as a promising method to achieve the clean-up of harmful algae and the remediation of eutrophic water. Here, we synthesize the NP–TiO2 (nitrogen and phosphorous doped TiO2)/C composites using a facile sol-gel method, and demonstrate successful achievement of efficient adsorption-photocatalytic performance via the in-situ formed carbides coated with NP–TiO2 nanoparticles. We find that the composites have rough surfaces with porous structure, which can be tuned by the calcination temperature, and that such composites can be served to efficiently capture the algal cells. The N and P are successfully doped into the TiO2 crystal lattices, and the cooperation of carbides and NP–TiO2 particles enhances significantly light absorption, while inhibiting the recombination of the photogenerated charge carriers. Among all the NP–TiO2/C composites, the NP–TiO2/C system calcinated at 550 °C shows the best photocatalytic performance for the algal inactivation, presenting a removal rate of 92.6% following 6 h visible light irradiation. The destruction of cell structures is clearly observed in the photocatalytic process. Interestingly, the metabolic activities are also disturbed by the photogenerated radicals, which accelerates the death of algal cells. Moreover, the NP–TiO2/C composite can effectively remove the cytotoxins from water, rendering the composite and the doping strategy promising in the remediation practice for eutrophic waters.
| Original language | English |
|---|---|
| Pages (from-to) | 351-359 |
| Number of pages | 9 |
| Journal | Chemosphere |
| Volume | 228 |
| DOIs | |
| State | Published - Aug 2019 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Adsorption
- Carbide
- Harmful algae
- Photocatalysis
- TiO
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