El-Debs Racha, Nehmé Reine, Claude Bérengère, Motteau Solène, Togola Anne, Berho Catherine, Morin Philippe
Institut de Chimie Organique et Analytique (ICOA), UMR 7311, Université d'Orléans, rue de Chartres, 45067 Orléans Cedex 2, France.
Institut de Chimie Organique et Analytique (ICOA), UMR 7311, Université d'Orléans, rue de Chartres, 45067 Orléans Cedex 2, France.
J Chromatogr A. 2014 Nov 7;1367:161-6. doi: 10.1016/j.chroma.2014.09.047. Epub 2014 Sep 28.
Sulfonylureas (SUs) are one of the most widely used herbicides to control weeds in crops. Herein, capillary electrophoresis (CE) was used to determine four sulfonylureas in natural waters, namely chlorsulfuron (CS), iodosulfuron methyl (IM), metsulfuron methyl (MSM) and mesosulfuron methyl (MSS). First of all, a bare silica capillary was chosen with 10mM of 1-butyl-3-methylimidazolium tetrafluoroborate (bminBF4) as electrophoretic buffer (pH 9.6) containing 2 mg L(-1) of surfactant-coated single-wall carbon nanotubes (SC-SWCNTs). A dramatic deviation in migration times was observed. Therefore, a poly(diallyldimethylammonium) chloride (PDADMAC) statically coated cationic capillary was used to improve repeatability and to alter the selectivity of the separation. The electroosmotic flow (EOF) measurement revealed that the SC-SWCNTs were strongly adsorbed at the surface of the PDADMAC coating even in the absence of the surfactant-coated nanotubes in the electrolyte buffer. Consequently, a stable strong cathodic EOF and excellent repeatabilities were obtained with relative standard deviations (RSDs) on migration times and on corrected peak areas below 0.9 and 1.5%, respectively. The separation of the SUs was conducted in only 6 min. No regeneration of the coating between analyses was necessary, and high peak efficiencies up to 173,000 theoretical plates were obtained. The bi-layer coating was subsequently used to analyze sulfonylureas in tap water, in several mineral waters as well as in underground waters spiked with SUs and directly injected into the CE capillary.
磺酰脲类除草剂是农作物中使用最广泛的除草剂之一。本文采用毛细管电泳法测定天然水中的四种磺酰脲类除草剂,即氯磺隆(CS)、甲基碘磺隆(IM)、甲磺隆(MSM)和甲基二磺隆(MSS)。首先,选用内径为10mM的1-丁基-3-甲基咪唑四氟硼酸盐(bminBF4)作为电泳缓冲液(pH 9.6)的裸硅毛细管,其中含有2mg/L的表面活性剂包覆单壁碳纳米管(SC-SWCNTs)。观察到迁移时间出现了显著偏差。因此,采用聚二烯丙基二甲基氯化铵(PDADMAC)静态涂层阳离子毛细管来提高重复性并改变分离的选择性。电渗流(EOF)测量表明,即使在电解质缓冲液中不存在表面活性剂包覆的纳米管的情况下,SC-SWCNTs也强烈吸附在PDADMAC涂层表面。因此,获得了稳定的强阴极EOF和优异的重复性,迁移时间和校正峰面积的相对标准偏差(RSD)分别低于0.9%和1.5%。磺酰脲类除草剂的分离仅需6分钟。分析之间无需对涂层进行再生,并且获得了高达173,000理论塔板数的高峰效。随后,采用双层涂层分析自来水中、几种矿泉水中以及加标磺酰脲类除草剂并直接注入CE毛细管的地下水中的磺酰脲类除草剂。