Add like
Add dislike
Add to saved papers

Strategies and relative mechanisms to attenuate the bioaccumulation and biotoxicity of ceria nanoparticles in wastewater biofilms.

Inhibitory effects of ceria nanoparticles (CeO2 NPs) on biofilm were investigated individually and in combination with phosphate (P), ethylene diamine tetraacetic acid (EDTA), humic acid (HA) and citrate (CA) to further explore the toxicity alleviating solutions. Exposure to 20 mg/L CeO2 NPs significantly decreased the performance of biofilm in nutrients removal. Distribution experiments suggested >98% of the CeO2 NPs retained in microbial aggregates, leading to 51.26 μg/L Ce ions dissolution. The dissolved CeIV and its further being reduced to CeIII stimulated the formation of O2 - and OH, which increased lipid peroxidation level to 130.93% in biofilms. However, P/EDTA/CA captured or precipitated Ce ions, whereas EDTA/HA/CA shielded NPs-bacteria direct contacts, both disturbing the NPs adsorption, intercepting the redox transition between CeIV and CeIII , reducing the generation of O2 - and OH, thus mitigating the toxicity of CeO2 NPs. These results illustrate the main drivers of CeO2 NPs biotoxicity and provide safer-by-design strategies.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app