“…Dieldrin has a higher persistence than TCE and is less amenable to reductive dechlorination under anaerobic conditions. Remediation techniques for dieldrin (UV/Fenton reagent, UV/chemical reaction, Pd/C catalyst, solar photocatalysis, and bioremediation) have been reported (Books, 1980;Maule et al, 1987;Bandala et al, 2002;Kusvuran and Erbatur, 2004;Chiu et al, 2005;Zinovyev et al, 2005;Dureja et al, 1987;Baczynski et al, 2004), but dieldrin transforms to mono-or di-dechlorinated intermediates still having a bicyclic ring structure. A study of the use of Fenton reagent for aldrin reports the transformation from aldrin to oxalic acid, acetic acid, chlorohexanone, cyclohexanol, cis-2-hydroxy-cyclohexanone, cis-2-methyl-cyclohexanol, 4-hydroxycyclohexanone, cis-4-methylcyclohexanol, 1-cyclopropyl-1-hydroxyethylene, and trans-dihydroxycyclohexane (Kusvuran and Erbatur, 2004).…”