Abstract
The electrochemically-assisted photocatalytic degradation of 4-chlorophenol (4-CP) using immobilized TiO2 particulate films has been investigated by analyzing reaction intermediates under a variety of experimental conditions. The degradations were carried out in both nitrogen- and oxygen-saturated solutions to explore the role of reduced oxygen species and molecular oxygen in the formation of reaction intermediates and in the mineralization of 4-CP. The degradation rate can be greatly improved even in a nitrogen-saturated atmosphere by applying an anodic bias to the TiO2 film electrodes. 4-Chlorocatechol (4-CC) is the predominant intermediate observed in oxygen-saturated solutions, whereas hydroquinone (HQ) is the primary intermediate in nitrogen-saturated solutions. Molecular oxygen plays an important role in the enhancement of the electrochemically assisted photocatalytic decay rate of 4-CP and the subsequent degradation of reaction intermediates, viz., 4-CC and HQ.
Original language | English (US) |
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Pages (from-to) | 6797-6803 |
Number of pages | 7 |
Journal | Journal of physical chemistry |
Volume | 98 |
Issue number | 27 |
DOIs | |
State | Published - 1994 |
ASJC Scopus subject areas
- General Engineering
- Physical and Theoretical Chemistry