Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.
J Chromatogr A. 2010 Feb 19;1217(8):1203-7. doi: 10.1016/j.chroma.2009.12.028. Epub 2009 Dec 16.
An analytical technique of in-line coupling headspace liquid-phase microextraction (HS-LPME) with capillary electrophoresis (CE) was proposed to determine volatile analytes. A special cover unit of the sample vial was adopted in the coupling method. To evaluate the proposed method, phenols were used as model analytes. The parameters affecting the extraction efficiency were investigated, including the configuration of acceptor phase, kind and concentration of acceptor solution, extraction temperature and time, salt-out effect, sample volume, etc. The optimal enrichment factors of HS-LPME were obtained with the sample volume of about half of sample vials, which were confirmed by both the theoretical prediction and experimental results. The enrichment factors were obtained from 520 to 1270. The limits of detection (LODs, S/N=3) were in the range from 0.5 to 1 ng/mL each phenol. The recoveries were from 87.2% to 92.7% and the relative standard deviations (RSDs) were lower than 5.7% (n=6). The proposed method was successfully applied to the quantitative analysis of the phenols in tap water, and proved to be a simple, convenient and reliable sample preconcentration and determination method for volatile analytes in water samples.
提出了一种在线耦合顶空液相微萃取(HS-LPME)与毛细管电泳(CE)的分析技术,用于测定挥发性分析物。在耦合方法中采用了样品瓶的特殊盖单元。为了评估所提出的方法,以酚类作为模型分析物。研究了影响萃取效率的参数,包括接受相的配置、接受溶液的种类和浓度、萃取温度和时间、盐析效应、样品体积等。通过大约一半的样品瓶体积,获得了 HS-LPME 的最佳富集因子,这一点通过理论预测和实验结果都得到了证实。富集因子的范围为 520 至 1270。每种酚的检测限(LOD,S/N=3)均为 0.5 至 1ng/mL。回收率为 87.2%至 92.7%,相对标准偏差(RSD)低于 5.7%(n=6)。该方法成功地应用于自来水中酚类的定量分析,证明了该方法是一种简单、方便、可靠的水样中挥发性分析物的样品预浓缩和测定方法。