Photocatalytic degradation of sulfamethoxazole using TiO2 in simulated seawater: evidence for direct formation of reactive halogen species and halogenated by-products

dc.contributor.author
Porcar Santos, Oriol
dc.contributor.author
Cruz Alcalde, Alberto
dc.contributor.author
López Vinent, Núria
dc.contributor.author
Zanganas, Dimitrios
dc.contributor.author
Sans Mazón, Carme
dc.date.issued
2022-04-05T11:14:13Z
dc.date.issued
2022-04-05T11:14:13Z
dc.date.issued
2020-03-10
dc.date.issued
2022-04-05T11:14:13Z
dc.identifier
1385-8947
dc.identifier
https://hdl.handle.net/2445/184662
dc.identifier
702460
dc.description.abstract
Combined sewer overflows (CSO), generated during the wet weather flow from the combination of the inflow and stormwater runoff in sewer system, result in an overflow of untreated wastewater from sewer system, which might ultimately contain different micropollutants (MPs). In this study, a coagulation-flocculation-sedimentation (CFS) pretreated CSO spiked with MPs was treated by catalytic ozonation using carbon, iron and peroxide based catalysts. The catalysts were characterized and their activity on MPs removal was studied at two different ozone (O3) doses (5 and 10 mg L‒1). The effect of the treatment on the spiked CSO effluent was also assessed from the acute toxicity of the effluent using Microtox®, Yeast and Macrophage cell-line toxicity assay tests. All the carbon-based catalysts showed large surface area, which was strongly influenced by the activation technique in the preparation of the catalyst. The CFS treatment strongly reduced the turbidity (≥ 60%) but had marginal effect on the UV254, dissolved organic carbon (DOC) and pH. Sludge Based Carbon (SBC) showed strong adsorption capacity (≥ 60% removal efficiency) for all MPs studied compared to other carbon and iron-based catalysts. Ozonation alone was effective for the degradation of easily oxidizable MPs (sulfamethoxazole, mecoprop, and 2,4-dichlorophenoxyl acetic acid), achieving more than 80% degradation efficiency at 10 mg L‒1 of ozone, but not effective for atrazine (≤ 60% degradation efficiency) at similar O3 dose. Catalytic ozonation (at 10 mg L‒1 O3 dose) improved the degradation of the MPs at low catalyst dosage but higher dosage strongly inhibited their degradation. In all cases, the effluents showed negligible acute toxicity, indicating the suitability of the process for the treatment of CSO.
dc.format
34 p.
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application/pdf
dc.language
eng
dc.publisher
Elsevier B.V.
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1016/j.scitotenv.2020.139605
dc.relation
Chemical Engineering Journal, 2020, vol. 736, num. 139605
dc.relation
https://doi.org/10.1016/j.scitotenv.2020.139605
dc.rights
cc-by-nc-nd (c) Elsevier B.V., 2020
dc.rights
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Enginyeria Química i Química Analítica)
dc.subject
Fotocatàlisi
dc.subject
Halògens
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Diòxid de titani
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Nanopartícules
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Photocatalysis
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Halogens
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Titanium dioxide
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Nanoparticles
dc.title
Photocatalytic degradation of sulfamethoxazole using TiO2 in simulated seawater: evidence for direct formation of reactive halogen species and halogenated by-products
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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