Degradation of 2,4-dichlorophenoxyacetic acid by photolysis and photo-Fenton oxidation - Archive ouverte HAL Access content directly
Journal Articles Journal of Environmental Chemical Engineering Year : 2018

Degradation of 2,4-dichlorophenoxyacetic acid by photolysis and photo-Fenton oxidation


This work aimed at comparing different UV and H2O2 based advanced oxidation processes (AOPs) −photolysis, UV/H2O2, and photo-Fenton reaction- for the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D), a common ingredient of phytosanitary products. The influence of oxidant dose (H2O2), catalyst type and concentration, pollutant concentration, water matrix and irradiation spectrum was also analyzed. Under reference conditions (25 mg/L of 2,4-D in osmosed water), photo-Fenton oxidation using Fe2+ salt, initial pH value of 2.6 and a low pressure mercury vapor lamp (10 W, λ=254 nm) yielded more than 85% of pollutant mineralization in one hour, as compared to 60% and less than 10% for UV/H2O2 and photolysis, respectively. Such a performance could be achieved in 10 min only when applying optimal concentration range for Fenton’s reagent (2 to 5 times the stoichiometric amount of H2O2 and oxidant-to-catalyst molar ratio from 25 to 40). Conversely, addition of a ZSM-5 zeolite bearing iron active sites albeit catalyzing Fenton oxidation at natural pH – did not bring additional benefit to UV/H2O2 process. Use of wastewater treatment plant effluent as aqueous matrix or irradiation in the UVA-visible range somewhat lowered the fficiency of the homogeneous photo-Fenton process. Nonetheless, bench scale experiments under sunlight gave promising results for 2,4 D remediation in wastewater, leading to over 80% conversion of the pollutant within ten minutes.
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hal-01879971 , version 1 (24-09-2018)



Germán Cruz González, Carine Julcour-Lebigue, Hélène Chaumat, Ulises Jáuregui-Haza, Henri Delmas. Degradation of 2,4-dichlorophenoxyacetic acid by photolysis and photo-Fenton oxidation. Journal of Environmental Chemical Engineering, 2018, 6 (1), pp.874-882. ⟨10.1016/j.jece.2017.12.049⟩. ⟨hal-01879971⟩
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