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Development and implementation of an integrative bioanalytical approach to identify sources of toxicity formed during ozonation of wastewater

Project description

Tracing toxicity during ozonation of wastewater

High concentrations of organic micropollutants (MPs) can have adverse effects on the aquatic environment, potentially polluting important drinking water sources. Since MPs can enter watercourses through conventional wastewater treatment plants, many EU countries have been forced to upgrade their facilities. While ozonation technology can reduce certain toxicities, toxicological studies detected mutagenetic and genotoxic activities (associated with carcinogenicity) in ozonated wastewater. Meanwhile, little is known about the nature of mutagenetic and genotoxic ozonation products (OTPs) and by-products (OBPs). The EU-funded OzoToxID project will develop and apply an integrative bioanalytical strategy combining mutagenicity and genotoxicity bioassays, fractionation and innovative high-resolution mass spectrometry chemical analysis to detect mutagenetic and genotoxic OTPs and OBPs, define their precursors and elucidate their formation processes.

Objective

Organic micropollutants (MPs) such as pharmaceuticals, industrial chemicals, and biocides cause undesired effects in the aquatic environment when present above certain concentrations. Conventional wastewater treatment plants (WWTPs) are major point sources of entry of MPs into watercourses, leading to disturbances in the ecosystems of receiving water bodies and potentially to a negative impact on the quality of drinking water resources. Several European countries have started upgrading their WWTPs to reduce discharges of MPs into water bodies. Ozonation is one of the two main technologies used to upgrade WWTPs. The abatement of MPs by ozone has been shown to reduce certain toxicities such as endocrine disruption and algal toxicity. However, toxicological studies which investigated mutagenicity and genotoxicty –two endpoints relevant to carcinogenicity– revealed that ozonated wastewater exhibited mutagenic and genotoxic activities, which were not present before ozonation. To date, the nature of mutagenic and genotoxic ozonation transformation products and byproducts (OTPs and OBPs) as well as their precursors has not been elucidated. Owing to the large number of MPs present in wastewater effluents, testing each compound individually is not a feasible option. Consequently, an integrative strategy that prioritizes identification and targets the mutagenic and genotoxic compounds after toxicity assessment is necessary. OzoToxID aims at developing and implementing an integrative bioanalytical strategy based on effect-directed analysis combining mutagenicity and genotoxicity bioassays, fractionation, and cutting-edge high-resolution mass spectrometry chemical analysis to identify mutagenic and genotoxic OTPs/OBPs, determine their precursors, and elucidate their formation pathways. OzoToxID will provide key data that is crucial to determine the feasibility of ozonation when upgrading WWTPs.

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MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

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(opens in new window) H2020-MSCA-IF-2019

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Coordinator

EIDGENOESSISCHE ANSTALT FUER WASSERVERSORGUNG ABWASSERREINIGUNG UND GEWAESSERSCHUTZ
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 203 149,44
Address
UBERLANDSTRASSE 133
8600 Dubendorf
Switzerland

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Region
Schweiz/Suisse/Svizzera Zürich Zürich
Activity type
Other
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 203 149,44
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