FTIR approaches for diuron determination in commercial pesticide formulations

被引:18
作者
Armenta, S [1 ]
Quintás, G [1 ]
Morales, A [1 ]
Garrigues, S [1 ]
De la Guardia, M [1 ]
机构
[1] Univ Valencia, Dept Analyt Chem, E-46100 Valencia, Spain
关键词
diuron; FTIR determination; flow injection analysis; stopped-f low; pesticide formulations;
D O I
10.1021/jf050268f
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Two strategies have been developed for Diuron determination by FTIR spectrometry, an off-line extraction and stopped-flow determination and a fully mechanized procedure, based on the on-line extraction of Diuron and FIA-FTIR measurement of the extracts. The aforementioned procedures have been compared with a reference chromatographic method. The off-line FTIR spectra were obtained at a nominal resolution of 4 cm(-1) from 4000 to 900 cm(-1) by accumulating 25 scans. Diuron was determined using peak height measurements at 1582 cm(-1) corrected using a baseline defined between 1562 and 1614 cm(-1). The waste generation of the off-line procedure was 3.4 mL chloroform for each sample, and the method provided a LOD of 40 mu g g(-1), corresponding to 0.8% (w/w) Diuron in the original sample. The fully mechanized FIA method provided a LOD of 35 mu g g(-1), which corresponds to 0.7% (w/w) in the solid sample and a maximum sampling frequency of the whole procedure of 30 h(-1), with a waste generation of 9.3 mL per sample, taking into account the volume of CHCl3 required for sample dissolution and that need as a carrier. All those methods consume less organic solvent than a HPLC method, which involves the use of 39 mL of acetonitrile per sample and a sampling frequency of 12 h(-1).
引用
收藏
页码:5842 / 5847
页数:6
相关论文
共 24 条
[1]   Quantitative analysis of agrochemical formulations by multivariate spectroscopic techniques [J].
Almond, MJ ;
Knowles, SJ .
APPLIED SPECTROSCOPY, 1999, 53 (09) :1128-1137
[2]  
[Anonymous], 1996, EXT TOX NETW PEST IN
[3]   Fourier transform infrared spectrometric strategies for the determination of Buprofezin in pesticide formulations [J].
Armenta, S ;
Quintás, G ;
Moros, J ;
Garrigues, S ;
de la Guardia, M .
ANALYTICA CHIMICA ACTA, 2002, 468 (01) :81-90
[4]   Gas chromatographic behaviour of urea herbicides [J].
Berrada, H ;
Moltó, JC ;
Font, G .
CHROMATOGRAPHIA, 2001, 54 (5-6) :360-364
[5]  
*COLL INT PEST AN, 1999, 3807 CIPAC
[6]  
DELINAN C, 2000, VADEMECUM PRODUCTOS
[7]   Electrospray liquid chromatography quadrupole ion trap mass spectrometry determination of phenyl urea herbicides in water [J].
Draper, WM .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (06) :2746-2755
[8]  
GALIGNANI M, 1993, ANALYST, V118, P1043
[9]   Determination of phenylurea herbicides in natural waters at concentrations below 1 ng 1-1 using solid-phase extraction, derivatization, and solid-phase microextraction gas chromatography mass spectrometry [J].
Gerecke, AC ;
Tixier, C ;
Bartels, T ;
Schwarzenbach, RP ;
Müller, SR .
JOURNAL OF CHROMATOGRAPHY A, 2001, 930 (1-2) :9-19
[10]  
LINVIEN D, 1991, INFRARED RAMAN CHARA