OH-radical-induced dechlorination of pentachlorophenol (PCP) has been
studies pulse and gamma-radiolytically. OH radicals react with PCP by
both electron transfer (53%) and addition followed by very rapid HCl-e
limination to form phenoxyl radicals. The phenoxyl radicals decay to f
orm products (e.g, chloranil) that unstable in alkaline aqueous soluti
on and release some more Cl-, therefore G(Cl-) is high. Primary HPLC-M
S analysis reveals that some quinones among the final products, whose
toxicity remains unclear. Ozone can also oxidize PCP very rapidly, and
this oxidation may destroy the benzene ring of PCP. (C) 1998 Elsevier
Science Ltd. All rights reserved.