Lim Lee Wah, Okouchi Yuki, Takeuchi Toyohide
Department of Chemistry, Faculty of Engineering, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan.
Talanta. 2007 Jul 31;72(5):1600-8. doi: 10.1016/j.talanta.2007.02.033. Epub 2007 Mar 7.
The ability and efficiency of micro precolumns made of C30 particles, monolithic silica C18 stationary phase and quartz wool coated with C30, which act as novel solid phase absorbing materials, for the on-line enrichment of aqueous polycyclic aromatic hydrocarbons (PAHs) in microcolumn liquid chromatography (LC) was investigated. The enrichment unit was designed in such a way that micro precolumns were directly connected to a 6-port micro injection valve via fused-silica tubing (0.05 mm I.D.) in order to minimize band broadening of the samples, and the enrichment efficiency of the three materials was tested using 14 PAHs, which are selected by the US Environmental Protection Agency (US EPA), as the analytes. The separation of PAHs was evaluated by using laboratory-made C30 or ODS capillary columns and the results were compared. There were no significant differences showed from the separation of PAHs in terms of peak signal between the C30 and ODS capillary columns, but the C30 capillary column was chosen for the following experiment due to its ability to produce better repeatability than the ODS column. By using the three kinds of precolumn materials, results showed that the precolumn packed with C30 particles as well as the capillary monolithic C18 precolumns (0.1 or 0.2mm I.D.) provided better recovery than those of the quartz wool's. As long as the recovery and separation of the PAHs were concerned, 0.1mm I.D. monolithic C18 precolumn showed the best results and the R.S.D.s (N=7) for the retention time, peak area and peak height were between 0.70-1.5, 2.3-5.8 and 2.4-6.6%, respectively. Large volume injection up to 0.5 mL, i.e. 2500-fold enrichment, was possible and no negative effect on the separation profile was found. The LOD (S/N=3) were between 0.10 and 4.6 pg mL(-1), while the LOQ (S/N=10) were in the range of 0.32-15 pg mL(-1), which showed that the system is comparable to many major analytical techniques and is sensitive enough for the trace analysis of PAHs in environmental samples. The system was then applied to the determination of trace PAHs present in soil sample which was randomly taken from a nearby highway.
研究了由C30颗粒、整体硅胶C18固定相和涂覆C30的石英棉制成的微型预柱作为新型固相吸附材料,用于微柱液相色谱(LC)中在线富集水中多环芳烃(PAHs)的能力和效率。富集单元的设计方式是,微型预柱通过内径为0.05mm的熔融石英管直接连接到六通微型进样阀,以尽量减少样品的谱带展宽,并使用美国环境保护局(US EPA)选定的14种PAHs作为分析物来测试这三种材料的富集效率。使用自制的C30或ODS毛细管柱评估PAHs的分离情况并比较结果。在PAHs的分离方面,C30和ODS毛细管柱在峰信号方面没有显著差异,但由于C30毛细管柱比ODS柱具有更好的重复性,因此选择其用于后续实验。使用这三种预柱材料的结果表明,填充C30颗粒以及内径为(0.1或0.2mm)的整体硅胶C18毛细管预柱比石英棉预柱具有更好的回收率。就PAHs的回收率和分离而言,内径为0.1mm的整体硅胶C18预柱显示出最佳结果,保留时间、峰面积和峰高的相对标准偏差(N = 7)分别在0.70 - 1.5%、2.3 - 5.8%和2.4 - 6.6%之间。可以进行高达0.5 mL的大体积进样,即2500倍富集,且未发现对分离谱图有负面影响。检测限(S/N = 3)在0.10至4.6 pg mL⁻¹之间,而定量限(S/N = 10)在0.32 - 15 pg mL⁻¹范围内,这表明该系统与许多主要分析技术相当,对环境样品中PAHs的痕量分析足够灵敏。然后将该系统应用于测定从附近高速公路随机采集的土壤样品中存在的痕量PAHs。