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Photolysis of chloroform and other organic molecules in aqueous TiO sub 2 suspensions

Journal Article · · Environmental Science and Technology; (USA)
DOI:https://doi.org/10.1021/es00015a018· OSTI ID:5555899
; ;  [1]
  1. California Insitute of Technology, Pasadena (USA)

The photocatalytic degradation of chloroform has been investigated in aqueous suspensions of TiO{sub 2} over the wavelength range of 310-380 nm. A detailed reaction mechanism has been proposed in which the rate-determining step is the reaction of surface-bound {sup {sm bullet}}OH with adsorbed CHCl{sub 3}. A pH-stat titration technique was developed for the measurement of the rates of degradation of chlorinated hydrocarbons. The quantum efficiency ({Phi} = 0.56 at {lambda} = 330 nm) of the degradation of CHCl{sub 3} was found to be inversely proportional to the square root of the incident light intensity. This relationship can be explained in terms of a direct competition between a second-order recombination of surface-bound {sup {sm bullet}}OH and the rate-determining reaction of surface-bound {sup {sm bullet}}OH with CHCl{sub 3}. The rates of degradation of several electron donors have been correlated with their computed surface speciation. The results of this study show that the adsorption of electron donors and acceptors to the TiO{sub 2} surface plays a more important role in determining the rate of the photocatalytic reactions than the effect of pH-dependent Fermi-level shifts.

OSTI ID:
5555899
Journal Information:
Environmental Science and Technology; (USA), Journal Name: Environmental Science and Technology; (USA) Vol. 25:3; ISSN ESTHA; ISSN 0013-936X
Country of Publication:
United States
Language:
English