Hydrolysis study and extraction of spiroxamine from soils of different physico-chemical properties

被引:8
作者
Rosales-Conrado, N. [1 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dpto Quim Analit, E-28040 Madrid, Spain
关键词
Spiroxamine; LC-MS/MS; Water degradation kinetics; Soil; TANDEM MASS-SPECTROMETRY; MULTI-RESIDUE METHOD; PESTICIDE-RESIDUES; PERFORMANCE; METABOLITES; VALIDATION; GRAPES; WATER; FOOD; WINE;
D O I
10.1016/j.chemosphere.2009.07.078
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Spiroxamine, 8-(1,1-dimethylethyl)-N-ethyl-N-propyl-1,4-dioxa-spiro [4.5] decane-2-methanamine, is a novel broad-spectrum fungicide from the new class of spiroketalamines widely used in cereals and grapes. In this paper, the hydrolysis of the spiroxamine active substance has been investigated and the extraction procedure from soil samples has been optimized. The progress of degradation in water at a wide pH range (4-14), was continuously monitored by means of reversed phase LC-ESI-MS/MS in the positive ionization mode during 90 d incubation experiment. To establish the degradation kinetics, water solutions were incubated by triplicate in the dark under controlled temperature (20 +/- 2 degrees C) and the spiroxamine remaining concentration was determined. Pesticide metabolites such as desethyl, despropyl and N-oxide spiroxamine were not detected at significant amounts in all tested conditions and the degradations followed first-order kinetics (r(2) >= 0.979). The faster degradation was observed at both pH 4 and 14 with half-life times of 37 and 10 d, respectively. On the other hand, the spiroxamine fungicide has been determined in two types of soil (silt loam and sandy loam) at different spiked levels. At the level of the highest spiroxamine application rate for agricultural crops (750 g a.i. ha(-1)), recoveries higher than 96.0% were obtained, showing the effectiveness of the proposed methodology. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:821 / 828
页数:8
相关论文
共 22 条
[1]  
ALLMENDIGER H, 1997, BAYER, V50, P49
[2]  
[Anonymous], 2001, Educating children with autism, P23
[3]   Mechanism of thifensulfuron-methyl transformation in soil [J].
Cambon, JP ;
Bastide, J ;
Vega, D .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1998, 46 (03) :1210-1216
[4]   Multi-residue method for the analysis of 101 pesticides and their degradates in food and water samples by liquid chromatography/time-of-flight mass spectrometry [J].
Ferrer, Imma ;
Thurman, E. Michael .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1175 (01) :24-37
[5]  
HANSSLER G, 1997, BAYER, V50, P15
[6]   Multiresidue liquid chromatography tandem mass spectrometry determination of 52 non gas chromatography-amenable pesticides and metabolites in different food commodities [J].
Hernández, F ;
Pozo, OJ ;
Sancho, JV ;
Bijlsma, L ;
Barreda, A ;
Pitarch, E .
JOURNAL OF CHROMATOGRAPHY A, 2006, 1109 (02) :242-252
[7]   Comprehensive multi-residue method for the target analysis of pesticides in crops using liquid chromatography-tandem mass spectrometry [J].
Hiemstra, Maurice ;
de Kok, Andre .
JOURNAL OF CHROMATOGRAPHY A, 2007, 1154 (1-2) :3-25
[8]  
KLEIN O, 1997, BAYER, V50, P71
[9]   Validation and uncertainty study of a comprehensive list of 160 pesticide residues in multi-class vegetables by liquid chromatography-tandem mass spectrometry [J].
Kmellar, B. ;
Fodor, P. ;
Pareja, L. ;
Ferrer, C. ;
Martinez-Uroz, M. A. ;
Valverde, A. ;
Fernandez-Alba, A. R. .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1215 (1-2) :37-50
[10]  
KRAMER W, 1997, BAYER, V50, P5