S. Parra et al., Photochemical versus coupled photochemical-biological flow system for the treatment of two biorecalcitrant herbicides: metobromuron and isoproturon, APP CATAL B, 27(3), 2000, pp. 153-168
Citations number
39
Categorie Soggetti
Physical Chemistry/Chemical Physics","Environmental Engineering & Energy
Physicochemical pre-treatment for the destruction of two non-biodegradable
herbicides (metobromuron and isoproturon) were conducted by different advan
ced oxidation processes, i.e. the systems UV/TiO2, UV/TiO2/H2O2, Fe3+/H2O2,
and UV/Fe3+/H2O2. The degradation rates were always higher for the photo-F
enton reactions when compared with the heterogeneous photocatalytic systems
. Optimal concentrations of Fe3+ and H2O2 for the abatement of both herbici
des in the photo-Fenton system were found. During the phototreatment, exper
iments were made to obtain information concerning the evolution of: (a) org
anic carbon and initial compound concentration, (b) the oxidation state, (c
) ions, (d) the toxicity, (e) the biodegradability, and (f) the chemical na
ture of the intermediates. These analysis show that the solution resulting
from the photodegradation of metobromuron is not appropriate for a biologic
al treatment, probably due to the formation and the accumulation in the bul
k of bromide intermediates, which are highly bio-recalcitrant. In contrast,
the solution resulting from the phototreatment of isoproturon is biologica
lly compatible and its complete mineralization can be performed by biologic
al means. A combined photo-Fenton and biological flow reactor for the degra
dation of isoproturon was operated in continuous mode at laboratory scale.
In this coupled system, 100% of the initial concentration of isoproturon an
d 95% of TOC were removed. Some field experiments under direct sunlight wer
e carried out at the Plataforma Solar de Almeria in Spain. The obtained res
ults demonstrated that the solar catalytic treatment is effective for the p
urification of water contaminated by the herbicides under study. (C) 2000 E
lsevier Science B.V. All rights reserved.