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Endosulfan and lindane degradation using ozonation. | LitMetric

Endosulfan and lindane degradation using ozonation.

Environ Technol

The Energy and Resources Institute (TERI), 4th Main, II Cross, Domlur II Stage, Bangalore 560071, Karnataka, India.

Published: August 2012

AI Article Synopsis

  • Ozone, a strong oxidizing agent, was used in this study to effectively degrade endosulfan (89% efficiency) and lindane (43%) at an optimal dosage of 57 mg min(-1)
  • The degradation process was significantly influenced by pH levels, with a pH of 10 being optimal for endosulfan degradation (93% efficiency) and a pH of 12 for lindane (82% efficiency)
  • Kinetic analysis showed that both compounds followed first-order kinetics, and gas chromatography mass spectroscopy identified degradation products, suggesting mechanisms like ring fission for the chemicals involved.

Article Abstract

The fact that ozone is a very powerful oxidizing agent (E0 = +2.07 V) was harnessed to degrade endosulfan and lindane in the present study. An ozone dosage of 57 mg min(-1) was found to be optimal for the degradation of both endosulfan (89%) and lindane (43%). The pH of the reaction mixtures play a profound role on the extent of degradation and it was observed that alkaline conditions favours the generation of hydroxyl radicals and thus a pH of 10 was chosen as the optimum for endosulfan degradation as the degradation efficiency was found to be 93%. A pH value of 12 was chosen as the optimum for lindane degradation as the degradation efficiency was observed to be 82%. Kinetics of degradation was performed and the set of data was fitted into first-order kinetics of the reaction for both endosulfan and lindane. The observed rate constants (k(obs')) for 5, 7.5 and 10 ppm initial endosulfan concentrations were 0.0274, 0.0273 and 0.0161 min(-1), respectively. While for initial lindane concentrations of 5, 7.5 and 10 ppm, the observed rate constants were 0.0243, 0.0333 and 0.056 min(-1), respectively. Gas chromatography mass spectroscopy analysis revealed that endosulfan was degraded into methyl cyclohexane and o-xylene which disappeared as reaction proceeded and lindane was degraded to 1-hexene indicating the ring fission mechanism.

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Source
http://dx.doi.org/10.1080/09593330.2011.603752DOI Listing

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