Surface modification of TiO2 nanoparticles for photochemical reduction of nitrobenzene

Citation
Ov. Makarova et al., Surface modification of TiO2 nanoparticles for photochemical reduction of nitrobenzene, ENV SCI TEC, 34(22), 2000, pp. 4797-4803
Citations number
37
Categorie Soggetti
Environment/Ecology,"Environmental Engineering & Energy
Journal title
ENVIRONMENTAL SCIENCE & TECHNOLOGY
ISSN journal
0013936X → ACNP
Volume
34
Issue
22
Year of publication
2000
Pages
4797 - 4803
Database
ISI
SICI code
0013-936X(20001115)34:22<4797:SMOTNF>2.0.ZU;2-A
Abstract
The effects of surface modification of nanocrystalline titanium dioxide (Ti O2) with specific chelating agents on photocatalytic degradation of nitrobe nzene (NB) was investigated in order to design a selective and effective ca talyst for removal of nitroaromatic compounds from contaminated waste strea ms. Mechanisms of NE adsorption and photodecomposition were investigated us ing infrared absorption and electron paramagnetic resonance spectroscopy. L iquid chromatography and gas chromatography/mass spectrometry were used for byproduct analyses. Arginine, lauryl sulfate, and salicylic acid were foun d to bind to TiO2 via their oxygen-containing functional groups. Modificati on of the TiO2 surface with arginine resulted in enhanced NE adsorption and photodecomposition, and compared to unmodified TiO2. The initial quantum y ield for photodegradation of NE in this system was found to be Phi (init) = 0.31 as compared to the one obtained for Degussa P25 of Phi (init) = 0.18. NE degradation followed a reductive pathway over arginine-modified TiO2 an d was enhanced upon addition of methanol. No degradation of arginine was de tected under the experimental conditions. Arginine improved the coupling be tween NE and TiO2 and facilitated the transfer of photogenerated electrons from the TiO2 conduction band to the adsorbed NE. These results indicate th at surface modification of nanocrystalline TiO2 with electron-donating chel ating agents is an effective route to enhance photodecomposition of nitroar omatic compounds.