Metsulfuron-methyl determination in environmental samples by solid surface fluorescence

被引:2
作者
Alesso, Magdalena [1 ]
Almeida, Cesar A. [1 ]
Talio, Maria C. [1 ]
Fernandez, Liliana P. [1 ]
机构
[1] Univ Nacl San Luis, Fac Quim Bioquim & Farm, Area Quim Analit, INQUISAL CONICET, Chacabuco 917,D5700BWS, San Luis, Argentina
关键词
Metsulfuron-methyl; Herbicide; Fluorescence; Solid phase extraction; SULFONYLUREA HERBICIDES; PHASE EXTRACTION; WATER SAMPLES; RHODAMINE-B; PHENYLUREA PESTICIDES; CARBON NANOTUBES; WEED-CONTROL; LIQUID; COACERVATION; SOIL;
D O I
10.1016/j.microc.2018.02.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new environmental friendly methodology for metsulfuron-methyl quantification based on the fluorescent signal enhancement of rhodamine B dye has been developed. A cationic surfactant (cetyltrimethylammonium bromide, CTAB) and an anionic one (sodium dodecylsulfate) were employed to preconcentrate the herbicide using a coacervation phenomenon, in sodium borate buffer medium (pH 9.2). The coacervate phase was collected on a nylon membrane (0.45 pm) and the solid surface fluorescence signal was determined (lambda(exc) = 515 nm, lambda(en), = 565 nm). Experimental variables that influence on preconcentration step and fluorimetric sensitivity have been studied and optimized using response surface methodology. Under optimal working conditions, a LOD of 0.17 mu g L-1 and a LOQ 0.53 mu g L-1 was obtained. The zeroth order regression calibration was linear from 0.53 to 5.0014 L-1 . The method showed adequate sensitivity and selectivity, and was applied to the determination of trace amounts of metsulfuron-methyl in environmental water samples. The proposed methodology implies an alternative to traditional techniques for metsulfuron-methyl monitoring using an accessible instrument in control laboratories, representing a contribution in the toxicological and environmental areas for the monitoring of MSM in environmental samples, in agreement with the Green Chemistry. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:150 / 154
页数:5
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