Efficient photocatalytic degradation of gaseous acetaldehyde by highly ordered TiO2 nanotube arrays.

Environ Sci Technol

Photocatalyst Group, Special Research Laboratory for Optical Science, Kanagawa Academy of Science and Technology, KSP Building West 614, 3-2-1 Sakado, Takatsu-ku, Kawasaki, Kanagawa 213-0012, Japan.

Published: November 2008

Highly ordered TiO2 nanotube array prepared by electrochemical anodization generates considerable interest as a practical air purifier, since a nanotube array can form a TiO2 film with a porous surface and straight gas diffusion channel, simultaneously reserving enough geometric thickness. Here, we reported on the application of highly ordered TiO2 nanotube arrays with different lengths for degradation of gaseous acetaldehyde pollutants in air. The results showed that increasing the lengths of nanotube arrays within a certain range could significantly improve the degradation rate of acetaldehyde molecules. The main product of acetaldehyde degradation was detected to be CO2, which indicated that the mineralization of acetaldehyde molecules was the major process in this photocatalytic reaction. When compared with a P25 TiO2 nanoparticulate film with similar thickness and geometric area, in the initial degradation of acetaldehyde, the nanotube array did not show obvious superiority. However, in the subsequent degradation, the nanotube array demonstrated an enhanced photocatalytic activity. It was suggested that this enhancement resulted from the special infrastructure of the nanotube array, which was favorable for the diffusion of intermediates and the reduced deactivation of photocatalyst in the photocatalytic reaction.

Download full-text PDF

Source
http://dx.doi.org/10.1021/es8016842DOI Listing

Publication Analysis

Top Keywords

nanotube array
20
highly ordered
12
ordered tio2
12
tio2 nanotube
12
nanotube arrays
12
degradation gaseous
8
gaseous acetaldehyde
8
nanotube
8
acetaldehyde molecules
8
photocatalytic reaction
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!