首页> 外文期刊>Analytical chemistry >100 000-Fold Concentration of Anions in Capillary Zone Electrophoresis Using Electroosmotic Flow Controlled Counterflow Isotachophoretic Stacking under Field Amplified Conditions
【24h】

100 000-Fold Concentration of Anions in Capillary Zone Electrophoresis Using Electroosmotic Flow Controlled Counterflow Isotachophoretic Stacking under Field Amplified Conditions

机译:在电场放大条件下使用电渗流控制的逆流等速电泳叠加在毛细管区带电泳中将阴离子浓缩10万倍

获取原文
获取原文并翻译 | 示例
       

摘要

An electroosmotic flow (EOF) controlled counterflow isotachophoretic stacking boundary (cf-ITPSB) system under field amplified conditions has been examined as a way to improve the sensitivity of anions separated by capillary zone electrophoresis. The system comprised a high concentration of a high-mobility leading ion (100 mM chloride) and a low concentration of low-mobility terminating ion (1-3 mM MES or CHES) added to the sample in an unmodified fused-silica capillary at pH 8.05, buffered with Tris. Computer simulation studies using the software GENTRANS showed an increase in sensitivity of at least 10-fold over the previous cf-ITPSB system for simple inorganic ions, nitrite and nitrate. The simulations also suggested that the cf-ITPSB became stationary within the capillary and that its stationary position was not adversely affected by the concentration of MES. This was in contrast to experimental results that showed a slow and continual movement of the cf-ITPSB. This was more pronounced at lower concentrations of terminator (i.e., <3 mM) and resulted in a loss of resolution due to the cf-ITPSB being closer to the detector upon separation. This discrepancy was attributed to the change in pH across the capillary due to electrolysis and low buffering capacity in the sample, a phenomenon that cannot be simulated by the GENTRANS software. Replacement of MES with CHES as a lower mobility ion with increased buffer capacity failed to reduce the movement of the cf-ITPSB but did provide a further 3-fold improvement in sensitivity. The potential of this approach for sensitivity enhancement was demonstrated for the co-EOF separation of a mixture of six inorganic and small organic ions, with detection limits at the single-figure nanogram per liter level. These detection limits are 100 000 times better than can be achieved by normal hydrodynamic injection (ions prepared in water) and 250 times better than has been achieved by other online preconcentration approaches. The application of the EOF-controlled cf-ITPSB with counter-EOF separation of two pharmaceutical pollutants, naproxen and diflunisal, was also demonstrated with an improvement in sensitivity of 1000 giving detection limits of 350 ng/L in sewage treatment wastewater without any offline pretreatment.
机译:已经研究了在现场放大条件下电渗流(EOF)控制的逆流等速电泳堆积边界(cf-ITPSB)系统,以提高通过毛细管区带电泳分离的阴离子的灵敏度。该系统包含高浓度的高迁移率前导离子(100 mM氯离子)和低浓度的低迁移率终止离子(1-3 mM MES或CHES),在未改性的熔融硅胶毛细管中,在pH值下将其添加到样品中8.05,用Tris缓冲。使用GENTRANS软件进行的计算机仿真研究表明,对于简单的无机离子,亚硝酸盐和硝酸盐,其灵敏度比以前的cf-ITPSB系统提高了至少10倍。模拟还表明,cf-ITPSB在毛细管内变得固定,并且其固定位置不受MES浓度的不利影响。这与显示cf-ITPSB缓慢且连续运动的实验结果相反。在较低浓度的终止剂(即<3 mM)下,这种现象更为明显,并且由于cf-ITPSB在分离时更靠近检测器,导致分离度降低。这种差异归因于由于电解和样品中的低缓冲能力而导致的毛细管上pH值的变化,这种现象无法通过GENTRANS软件进行模拟。用CHES取代MES作为低迁移率离子并具有增加的缓冲容量无法降低cf-ITPSB的运动,但确实使灵敏度进一步提高了3倍。对于六种无机离子和小有机离子的混合物的共EOF分离,证明了这种方法提高灵敏度的潜力,其检测极限为每升一级图。这些检测限比普通流体动力注射(水中制备的离子)所能达到的检测限高100000倍,比其他在线预浓缩方法所能达到的检测限高250倍。还证明了EOF控制的cf-ITPSB的应用,同时对两种药物污染物萘普生和双氟尼醛进行反EOF分离,灵敏度提高了1000,对污水处理废水的检测限为350 ng / L,无需任何离线预处理。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号