Abstract
Aqueous solutions of γ-hexachlorocyclohexane (Lindane) were photolyzed (λ = 254 nm) under a variety of solution conditions. The initial concentrations of hydrogen peroxide (H2O2) and Lindane varied from 0 to 20 mM and 0.21 to 0.22 μM, respectively, the pH ranged from 3 to 11, and several concentration ratios of Suwannee River humic acid and fulvic acid were dissolved in the irradiated solutions. Lindane rapidly reacted, and the maximum reaction rate constant (9.7 × 10-3 s-1) was observed at pH 7 and initial [H2O2] = 1 mM. Thus, 90% of the Lindane is destroyed in ∼4 min under these conditions. In addition, within 15 min, all chlorine atoms were converted to chloride ion, indicating that chlorinated organic by-products do not accumulate. The reactor was characterized by measuring the photon flux (7.04 × 10-6 E s-1) and the cumulative production of {radical dot}OH during irradiation. The cumulative {radical dot}OH production during irradiation was fastest at an initial [H2O2] = 5 mM (k = 0.77 μM s-1). © 2008 Elsevier Ltd.
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Nienow, A. M., Bezares-Cruz, J. C., Poyer, I. C., Hua, I., & Jafvert, C. T. (2008). Hydrogen peroxide-assisted UV photodegradation of Lindane. Chemosphere, 72(11), 1700–1705. https://doi.org/10.1016/j.chemosphere.2008.04.080
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