期刊
CHEMOSPHERE
卷 308, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.136402
关键词
Heterogeneous photocatalysis; Dichlorvos; Malathion; Langmuir-Hinshelwood kinetics; Toxicity; Grapheneoxide-TiO2
资金
- Water Technology Initiative, Department of Science and Technology (DST) , New Delhi, India
- [DST/TM/WTI/2K15/101 (G)]
Heterogeneous photocatalysis using graphene oxide-TiO2 nanocomposite (GOT) was effective in removing dichlorvos and malathion pesticides from water. Optimum results were achieved at pH 6 and a catalyst dose of 60 mg/L, with high degradation rates and mineralization levels observed under UV irradiation.
Heterogeneous photocatalysis was used for the removal of two widely used organophosphorus pesticides, dichlorvos, and malathion from water. Graphene oxide-TiO2 nanocomposite (GOT) was synthesized and used as a photocatalyst for the removal of these pesticides. Batch studies for optimizing photocatalytic degradation and mineralization of pesticides over 80 min were conducted by varying the pH (2-10), catalyst dose (20 mg/L-200 mg/L), and initial pesticide concentration (0.5 mg/L-20 mg/L), and the irradiation source (125 W UV and visible lamp). Degradation kinetics for the pesticides were evaluated. Ellman assay was used to estimate the toxic effect of pesticides and evaluate toxicity reduction due to treatment. The highest degradation and mineralization of dichlorvos and malathion was observed at pH 6 and the optimum catalyst dose was 60 mg/L. Under UV irra-diation, 80% and 90% degradation were observed for dichlorvos and malathion, respectively for 0.5 mg/L initial pesticide concentration. The photocatalytic degradation reaction followed Langmuir-Hinshelwood kinetics. A high degree of mineralization was achieved for both the pesticides. Analysis of the results revealed that the residual toxic effect after photocatalysis was primarily due to the residual parent compound. A comparative study revealed that GOT yielded better pesticide degradation compared to commercially available TiO2 under both UV and visible irradiation.
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