Issue 29, 2021

The intimate coupling of photocatalysis and biodegradation for the degradation and mineralization of atrazine in water

Abstract

Atrazine is one of the most widely used herbicides and a main pollutant of soil and water bodies. Intimately coupled photocatalysis and biodegradation (ICPB) is an attractive technology for the treatment of wastewater, in which the microorganisms can decompose and mineralize the biodegradable intermediates generated by a photocatalytic reaction. A few works have investigated the removal of atrazine through ICPB technology, and in this work a heterojunction Bi2WO6/CN was designed and combined with biodegradation to remove atrazine. Bi2WO6/CN was adhered on the external section of a sponge carrier via a powder spraying method and a biofilm was then cultivated in the interior of the sponge carrier. The Bi2WO6/CN heterojunction can produce active species like ˙OH, holes and ˙O2 to break atrazine into biodegradable intermediates, which are quickly mineralized by biofilms in the interior of the carrier. The Bi2WO6/CN photocatalyst excited by UV-Vis light can take full advantage of the solar energy, and this heterostructure can facilitate the separation of photoinduced electron–hole pairs, hence further improving the generation of ˙OH and ˙O2. The sponge carrier can not only protect the biofilms inside from the damage of UV light and free radicals, but also can be easily recycled without secondary pollution. This work shows the potential of a Bi2WO6/CN based ICPB system for atrazine degradation from a practical point of view.

Graphical abstract: The intimate coupling of photocatalysis and biodegradation for the degradation and mineralization of atrazine in water

Supplementary files

Article information

Article type
Paper
Submitted
09 Jan 2021
Accepted
08 Jun 2021
First published
12 Jun 2021

New J. Chem., 2021,45, 13029-13039

The intimate coupling of photocatalysis and biodegradation for the degradation and mineralization of atrazine in water

L. Zhang, Y. Zhang, K. Xiao, J. Shi, X. Du, L. Wang and X. Wu, New J. Chem., 2021, 45, 13029 DOI: 10.1039/D1NJ00134E

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