Photocatalytic decomposition of 2-chlorophenol in aqueous solution by UV/TiO"2 process with applied external bias voltage [An article from: Journal of Hazardous Materials]
Book Details
Author(s)Y. Ku, Y.C. Lee, W.Y. Wang
PublisherElsevier
ISBN / ASINB000PBZUQI
ISBN-13978B000PBZUQ2
MarketplaceFrance 🇫🇷
Description
This digital document is a journal article from Journal of Hazardous Materials, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
The decomposition of 2-chlorophenol by UV/TiO"2 process with the application of external bias voltage was examined in this study. Experiments were conducted in a batch reactor using TiO"2-coated titanium sheet as anode and platinum sheet as cathode. The anode photocatalysis of 2-chlorophenol was totally inhibited for experiments conducted with the application of external anodic bias voltage lower than the flat band potential of TiO"2. The decomposition rate of 2-chlorophenol was then increased with increasing external anodic bias voltage applied up to 0.0V (versus SCE). The application of external bias voltage higher than 1.0V did not markedly promote the photocatalysis of 2-chlorophenol possibly because the photocurrent induced was constant. Experimental results indicated that the decomposition of 2-chlorophenol was more effective for experiments conducted in acidic solutions due to the lower flat band potential of TiO"2 and the higher photocurrent induced. The presence of electron scavengers in aqueous solution, such as oxygen molecules, may increase the decomposition rate of 2-chlorophenol. However, the effect of dissolved oxygen was diminished for experiments conducted with applied external bias voltage. The photocatalytic decomposition rate of 2-chlorophenol was enhanced linearly with the increasing UV light intensity when the external bias voltage was applied.
Description:
The decomposition of 2-chlorophenol by UV/TiO"2 process with the application of external bias voltage was examined in this study. Experiments were conducted in a batch reactor using TiO"2-coated titanium sheet as anode and platinum sheet as cathode. The anode photocatalysis of 2-chlorophenol was totally inhibited for experiments conducted with the application of external anodic bias voltage lower than the flat band potential of TiO"2. The decomposition rate of 2-chlorophenol was then increased with increasing external anodic bias voltage applied up to 0.0V (versus SCE). The application of external bias voltage higher than 1.0V did not markedly promote the photocatalysis of 2-chlorophenol possibly because the photocurrent induced was constant. Experimental results indicated that the decomposition of 2-chlorophenol was more effective for experiments conducted in acidic solutions due to the lower flat band potential of TiO"2 and the higher photocurrent induced. The presence of electron scavengers in aqueous solution, such as oxygen molecules, may increase the decomposition rate of 2-chlorophenol. However, the effect of dissolved oxygen was diminished for experiments conducted with applied external bias voltage. The photocatalytic decomposition rate of 2-chlorophenol was enhanced linearly with the increasing UV light intensity when the external bias voltage was applied.
