Rapid removal of flutriafol in water by zero-valent iron powder
A study of the effect of zero-valent iron (ZVI) powder is carried out for the first time on the degradation of flutriafol (( RS)-2,4′-difluoro-α-(1 H-1,2,4-triazol-1-ylmethyl)-benzhydryl alcohol, C 16H 13F 2N 3O), a bifluorinated soil and water persistent triazole pesticide using a laboratory scale...
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Published in | Chemosphere (Oxford) Vol. 71; no. 5; pp. 816 - 826 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier Ltd
01.03.2008
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | A study of the effect of zero-valent iron (ZVI) powder is carried out for the first time on the degradation of flutriafol ((
RS)-2,4′-difluoro-α-(1
H-1,2,4-triazol-1-ylmethyl)-benzhydryl alcohol, C
16H
13F
2N
3O), a bifluorinated soil and water persistent triazole pesticide using a laboratory scale device consisting of a 20
ml pyrex serum vials fixed to a Vortex agitator. Different amounts of ZVI powder (10–50
g
l
−1) at pH 6.6 and room temperature were investigated. Experiments showed an observed degradation rate
k
obs directly proportional to the surface of contact of flutriafol with ZVI. Flutriafol degradation reactions demonstrated first order kinetic with a half-live of about 10.8
±
0.5
min and 3.6
±
0.2
min when experiments were conducted at [ZVI]
=
10
g
l
−1 into oxygenated and anoxic solutions, respectively. Three analytical techniques were employed to monitor flutriafol degradation and to understand solution and by-products behaviors: (1) A UV–Vis spectrophotometer; (2) a high performance liquid chromatography (HPLC) coupled with a photo diode array (PDA) and fluorescence detectors; (3) a similar HPLC coupled with a PDA and a mass spectrometer detectors equipped with an atmospheric pressure photoionization source. Results showed a complete disappearance of flutriafol after 20
min of contact with ZVI, the loss of fluorescence properties of the final by-products, the defluorination of the triazole pesticide via hydroxylation reaction and finally the hydrogenation of the triazole ring. |
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Bibliography: | http://dx.doi.org/10.1016/j.chemosphere.2007.11.057 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2007.11.057 |