Abstract
Decomposition of monocrotophos in an aqueous solution by the hydrogen peroxide–ozone (H2O2–O3) process was studied under various solution pHs and H2O2–O3) molar ratios. Experimental results indicated that monocrotophos could be almost completely (>95%) decomposed by the H2O2–O3) process within 20 minutes. Formation of carbon dioxide was observed, followed by the formation of nitrate and phosphate. A simplified kinetic model, consisting of three two‐step consecutive reactions based on elemental mass balances, was found to accurately describe the temporal behaviors of reacting species during the decomposition of monocrotophos in aqueous solution by the H2O2–O3) process. In most experiments, acidic conditions favored the disappearance of monocrotophos, possibly because of breakage of the carbon–carbon double bond to form various organic intermediates, but mineralization of organic intermediates by free radical hydroxyl (OH·) attack was more favored in alkaline conditions. The decomposition of monocrotophos by the H2O2–O3) process was found to be significantly affected by the mode of H2O2 addition. For the batch mode of H2O2 addition, increased H2O2 dose reduced the decomposition rate, possibly because large amounts of H2O2 added initially served as a scavenger for OH· free radicals. For the continuous mode of H2O2 addition, increased H2O2 dose accelerated reaction rates of monocrotophos until an optimum H2O2–O3) molar ratio was reached, which was found to vary for different solution pHs.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.