Abstract

A synergistic effect of photocatalysis and ozonation on the decomposition of formic acid dissolving in an aqueous solution has been studied. In the photocatalysis over a thin film of titanium oxide immobilized on the inner surface of a glass tube, a 6 W blacklight blue fluorescent lamp (wavelength: 300–400 nm) was used as a light source. The initial decomposition rates followed a Langmuir–Hinshelwood type and the hydrogen peroxide generated during the photocatalytic reaction played an important role in the decomposition of formic acid. In the ozonation, a 6 W low-pressure mercury lamp (wavelength: 185 nm) was used to produce ozone by irradiation of the air with UV. When this air was circulated in a closed system with a water-holding glass container, the ozone concentrations in the air and water reached 0.350 g m −3 air and 0.037 g m −3 liquid, respectively, at maximum. The decomposition rate of formic acid by ozone was higher for a lower liquid temperature and a higher pH value. For comparison, the Langmuir–Hinshelwood type was also used to analyze both the experimental values obtained in the ozonation alone and in the combination of photocatalysis and ozonation. A relationship between the reaction rate and reactant concentration was calculated using the kinetic parameters determined from the experimental values in each reaction system. As a result, the decomposition rate of formic acid by the combination of photocatalysis and ozonation was found to be 31% higher at maximum than the sum of the decomposition rates when formic acid was individually decomposed by the two methods, which indicates the presence of a synergistic effect of the photocatalysis and ozonation. This effect may be explained by the promoted production of hydroxyl radicals by ozone over titanium oxide.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call