Wang Dong-Dong, Li Feng, Yan Xiu-Ping
Key Laboratory of Functional Polymer Materials (Nankai University), Ministry of Education, Research Center for Analytical Sciences, College of Chemistry, Nankai University, Tianjin 300071, China.
J Chromatogr A. 2006 Jun 9;1117(2):246-9. doi: 10.1016/j.chroma.2006.04.023. Epub 2006 May 8.
A hyphenated technique was developed for high-throughput speciation analysis by on-line coupling of flow injection (FI), miniaturized capillary electrophoresis (CE) and atomic fluorescence spectrometry (AFS). Two interfaces were used to couple all three systems: the first to couple FI and CE and the second to couple miniaturized CE and AFS. The first interface was a modified flow through chamber, connected to the FI valve with a piece of PTFE tube (0.1mm i.d.x 20 cm long). The capillary outlet was coupled to the AFS by using the second concentric "tube-in-tube" interface. Split sampling was achieved in the electrokinetic mode. Inorganic mercury (Hg(II)) and methylmercury (MeHg(I)) were taken as model analytes to demonstrate the performance of the developed hyphenated technique. A volatile species generation (VSG) technique was employed to convert the analytes from the CE effluent into their respective volatile species. Baseline separation of Hg(II) and MeHg(I) was achieved by CE in a 50 microm i.d.x 8 cm long capillary at 3.0 kV within 60s. The precisions (RSD, n=12) were in the range of 0.7-0.9% for migration time, 3.8-4.2% for peak area, and 2.1-3.5% for peak height. The detection limits were 0.1 and 0.2 microgmL(-1) (as Hg) for Hg(II) and MeHg(I) with a sample throughput of 60 samples h(-1). The recoveries of both mercury species in the water samples studied were in the range of 93-106%.
通过流动注射(FI)、微型毛细管电泳(CE)和原子荧光光谱法(AFS)的在线联用,开发了一种用于高通量形态分析的联用技术。使用两个接口来连接所有三个系统:第一个用于连接FI和CE,第二个用于连接微型CE和AFS。第一个接口是一个改进的流通池,通过一段聚四氟乙烯管(内径0.1mm×长20cm)连接到FI阀。毛细管出口通过使用第二个同心“管中管”接口与AFS相连。在电动模式下实现了分流进样。以无机汞(Hg(II))和甲基汞(MeHg(I))作为模型分析物来证明所开发联用技术的性能。采用挥发性物种发生(VSG)技术将CE流出物中的分析物转化为各自的挥发性物种。在50μm内径×8cm长的毛细管中,在3.0kV电压下,CE在60s内实现了Hg(II)和MeHg(I)的基线分离。迁移时间的精密度(RSD,n = 12)在0.7 - 0.9%范围内,峰面积的精密度在3.8 - 4.2%范围内,峰高的精密度在2.1 - 3.5%范围内。Hg(II)和MeHg(I)的检测限分别为0.1和0.2μg mL⁻¹(以Hg计),样品通量为60个样品/小时。所研究水样中两种汞形态的回收率在93 - 106%范围内。