ELECTROCHEMICALLY ASSISTED PHOTOCATALYSIS .2. THE ROLE OF OXYGEN AND REACTION INTERMEDIATES IN THE DEGRADATION OF 4-CHLOROPHENOL ON IMMOBILIZED TIO2 PARTICULATE FILMS
K. Vinodgopal et al., ELECTROCHEMICALLY ASSISTED PHOTOCATALYSIS .2. THE ROLE OF OXYGEN AND REACTION INTERMEDIATES IN THE DEGRADATION OF 4-CHLOROPHENOL ON IMMOBILIZED TIO2 PARTICULATE FILMS, Journal of physical chemistry, 98(27), 1994, pp. 6797-6803
The electrochemically-assisted photocatalytic degradation of 4-chlorop
henol (4-CP) using immobilized TiO2 particulate films has been investi
gated by analyzing reaction intermediates under a variety of experimen
tal conditions. The degradations were carried out in both nitrogen- an
d oxygen-saturated solutions to explore the role of reduced oxygen spe
cies and molecular oxygen in the formation of reaction intermediates a
nd 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 pred
ominant intermediate observed in oxygen-saturated solutions, whereas h
ydroquinone (HQ) is the primary intermediate in nitrogen-saturated sol
utions. 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 H
Q.