The photodegradation of 2,4-dichlorophenoxyacetic acid using titanium
dioxide as photocatalyst was investigated. The yield of 2,4-D photodeg
radation depends on the mass of the semiconductor, temperature and lig
ht intensity, The highest conversion rates were obtained at pH=3.5, wh
ich is close to the pK(a) of the acid and lower than the point of zero
charge of TiO2. The experimental data fit a Langmuir-Hinshelwood kine
tic model. The rate and equilibrium adsorption constants were obtained
from those data at different temperatures. Some aromatic intermediate
products of 2,4-D photodegradation were detected (2,4-dichlorophenol,
hydrohydroquinone, chlorohidroquinone). An analysis of total organic
carbon (TOC) showed that a complete mineralization of 2,4-D can be eas
ily achieved. On the other hand, the results obtained in experiments u
sing platinized TiO2 lead us to assume that both oxidation and reducti
on steps should be taken into account if an explanation of the experim
ental data is to be made.