Metalaxyl (N-(2,6-dimethylphenyl)-N-(methoxy-acetyl)-D,L-alanine methyl est
er, C15H21NO4) is extensively used as fungicide, and the resulting water co
ntamination is a potential health hazard. The photocatalytic decomposition
of this fungicide in aqueous suspensions containing TiO2 yields its complet
e mineralization. The intermediates formed during the photomineralization a
nd the reaction pathways were analyzed by recording proton NMR spectra. On
the basis of the measurements of total organic carbon it was concluded that
the rate of metalaxyl decomposition can be explained in terms of the Langm
uir-Hinshelwood kinetic model and the values of the resulting constants wer
e compared with those of some other organic compounds reported in the liter
ature. (C) 1999 Elsevier Science Ltd. All rights reserved.