Chicharro M, Bermejo E, Sánchez A, Zapardiel A, Fernandez-Gutierrez A, Arraez D
Departamento de Química Analítica y Análisis Instrumental, Facultad de Ciencias, Universidad Autónoma de Madrid, Madrid 28049, Spain.
Anal Bioanal Chem. 2005 May;382(2):519-26. doi: 10.1007/s00216-004-2840-6. Epub 2004 Sep 25.
A rapid multiresidue method has been developed for the analysis of seven phenylurea herbicides in the presence of two s-triazines in environmental waters. A simple end-column electrochemical detector was used in combination with a commercially-available capillary electrophoresis instrument with UV detection. The determination of phenylurea pesticides using micellar electrokinetic capillary chromatography with electrochemical detection represents the first such determination that has been reported. In both detection systems, linear ranges were obtained for the seven phenylurea herbicides at concentrations lower than 2.0x10(-5) mol l(-1), in 0.020 mol l(-1) phosphoric acid at pH 7.0 and containing 0.020 mol l(-1) of sodium dodecylsulfate, in order to obtain selectivity in the additional separation by a micellar distribution process. Under these conditions a detection limit lower than 5.0x10(-6) mol l(-1) (0.25 pmol of pesticide) was achieved for most of them. The pesticides were resolved in less than 30 min.
已开发出一种快速多残留方法,用于分析环境水样中在两种均三嗪存在下的七种苯基脲类除草剂。使用一种简单的柱端电化学检测器与一台配有紫外检测的市售毛细管电泳仪联用。采用胶束电动毛细管色谱法结合电化学检测来测定苯基脲类农药,这是首次报道此类测定方法。在这两种检测系统中,在pH 7.0的0.020 mol l(-1)磷酸中,含有0.020 mol l(-1)十二烷基硫酸钠,七种苯基脲类除草剂在浓度低于2.0x10(-5) mol l(-1)时获得了线性范围,以便通过胶束分配过程在额外分离中获得选择性。在这些条件下,大多数农药的检测限低于5.0x10(-6) mol l(-1)(0.25 pmol农药)。农药在不到30分钟内得到分离。