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Title: Radiolytic and TiO[sub 2]-assisted photocatalytic degradation of 4-chlorophenol. A comparative study

Journal Article · · Journal of Physical Chemistry; (United States)
DOI:https://doi.org/10.1021/j100076a019· OSTI ID:6980504
; ;  [1]
  1. Univ. of Notre Dame, IN (United States)

Mechanistic and kinetics details of 4-chlorophenol (4-CP) oxidation have been elucidated by radiolytic and photocatalytic techniques. When 4-chlorophenol is oxidized by [gamma]-radiolysis in conditions favoring hydroxyl radical oxidation ([sup [sm bullet]]OH), significant concentrations of 4-chlorocatechol (4-CC) and hydroquinone (HQ) are formed as intermediates. Phenol is the only major intermediate when conditions favoring reduction by hydrated electrons are employed. 4-CC and HQ are not detected when 4-chlorophenol is oxidized with azide radicals. Hydroxyl radical mediated oxidative degradation rates of 4-CP are similar at pH 3.0 and pH 6.1. The 4-CP degradation rate is relative slower at pH 9.1, and no aromatic intermediates are detected. These results confirm the proposal that hydroxy-mediated 4-CP oxidation follows at least three separate degradation pathways, forming 4-CC, HQ, and unidentified, mostly nonaromatic compounds, as reaction intermediates enroute to complete mineralization. Pulse radiolysis experiments have also been carried out to characterize the radical transient species formed during the oxidation of 4-CP (pH 6 and 10) and 4-chlorocatechol (pH 6). 41 refs., 6 figs., 3 tabs.

OSTI ID:
6980504
Journal Information:
Journal of Physical Chemistry; (United States), Vol. 98:25; ISSN 0022-3654
Country of Publication:
United States
Language:
English

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