Abstract
A magnetic sonophotocatalyst Fe3O4@SiO2@TiO2 is synthesized for the enhanced biodegradability of organophosphate pesticide. The as-prepared catalysts were characterized using different techniques, such as Xray diffraction (XRD) and transmission electron microscopy (TEM). The radial sonophotocatalytic activity of Fe3O4@SiO2@TiO2 nanocomposite was investigated, in which commercial dichlorvos (DDVP) was chosen as an object. The degradation efficiency was evaluated in terms of chemical oxygen demand (COD) and enhancement of biodegradability. The effect of different factors, such as reaction time, pH, the added amount of catalyst on CODCr removal efficiency were investigated. The average CODCr removal efficiency reached 63.13% after 240 min in 12 L sonophotocatalytic reactor (catalyst 0.2 g L, pH 7.3). The synergistic effect occurs in the combined sonolysis and photocatalysis which is proved by the significant improvement in CODCr removal efficiency compared with that of solo photocatalysis. Under this experimental condition, the BOD5/ CODCr ratio rose from 0.131 to 0.411, showing a remarkable improvement in biodegradability. These results showed that sonophotocatalysis may be applied as pre-treatment of pesticide wastewater, and then for biological treatment. The synthesized magnetic nanocomposite had good photocatalytic performance and stability, as when it was used for the fifth time, the CODCr removal efficiency was still about 62.38%.
Published Version (
Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
