Inhibition of bromate formation by reduced graphene oxide supported cerium dioxide during ozonation of bromide-containing water

Highlights

GO or RGO promotes bromate formation during ozonation of bromide-containing water.

CeO₂/RGO significantly inhibits bromate formation compared to RGO during ozonation.

CeO₂/RGO shows an enhancement on DEET degradation efficiency during ozonation.

Abstract

Ozone (O₃) is widely used in drinking water disinfection and wastewater treatment. However, when applied to bromide-containing water, ozone induces the formation of bromate, which is carcinogenic. Our previous study found that graphene oxide (GO) can enhance the degradation efficiency of micropollutants during ozonation. However, in this study, GO was found to promote bromate formation during ozonation of bromide-containing waters, with bromate yields from the O₃/GO process more than twice those obtained using ozone alone. The promoted bromate formation was attributed to increased hydroxyl radical production, as confirmed by the significant reduction (almost 75%) in bromate yield after adding t-butanol (TBA). Cerium oxide (less than 5 mg/L) supported on reduced GO (xCeO₂/RGO) significantly inhibited bromate formation during ozonation compared with reduced GO alone, and the optimal Ce atomic percentage (x) was determined to be 0.36%, achieving an inhibition rate of approximately 73%. Fourier transform infrared (FT-IR) spectra indicated the transformation of GO into RGO after hydrothermal treatment, and transmission electron microscope (TEM) results showed that CeO₂ nanoparticles were well dispersed on the RGO surface. The X-ray photoelectron spectroscopy (XPS) spectra results demonstrated that the Ce³⁺/Ce⁴⁺ ratio in xCeO₂/RGO was almost 3‒4 times higher than that in pure CeO₂, which might be attributed to the charge transfer effect from GO to CeO₂. Furthermore, Ce³⁺ on the xCeO₂/RGO surface could quench Br⋅ and BrO⋅ to further inhibit bromate formation. Meanwhile, 0.36CeO₂/RGO could also enhance the degradation efficiency of N,N-diethyl-m-toluamide (DEET) in synthetic and reclaimed water during ozonation.

Graphical abstract

Keywords

Bromate / Catalytic ozonation / Graphene oxide / Cerium dioxide

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Acknowledgements

This work was supported by grants from the National Key Research and Development Program of China (No.2016YFE0118800), the National Science Fund of China (Nos. 51578310), the Special Support Program for High-Level Personnel Recruitment in Guangdong Province (No.2016TQ03Z384), the Shenzhen Science, Technology and Innovation Commission (No. JCYJ20170818091859147), and the Water Cycle Program of Development and Reform Commission of Shenzhen Municipality.

Electronic Supplementary Material

Supplementary material is available in the online version of this article at https://doi.org/10.1007/s11783-019-1170-z and is accessible for authorized users.

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