G. Goutailler et al., Photocatalysed degradation of cyromazine in aqueous titanium dioxide suspensions: comparison with photolysis, J PHOTOCH A, 141(1), 2001, pp. 79-84
Citations number
20
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
The fate of cyromazine (N-cyclopropyl-1,3,5-triazine-2,4,6-triamine), an in
sect growth regulator, has been studied upon irradiation as well as its pho
tocatalytic treatment (advanced oxidation technology). Most of the organic
compounds occurring during the photodegradation have been identified by mea
ns of liquid chromatography and mass spectrometry coupled techniques (LC-MS
). The main photoproducts of the first degradation steps are amide-triazine
s and melamine. Simultaneously, carboxylic acids, such as acrylic, pyruvic
and glycolic acids have been identified by LC-UV. These acids are resulting
from the cyclopropyl degradation. The melamine (1,3,5-triazine-2,4,6-triam
ine) is transformed into cyanuric acid (2,4,6-trihydroxy-1,3,5-triazine) by
means of three successive deaminations. This compound remains very stable
in aqueous solution, (C) 2001 Elsevier Science B.V, All rights reserved.