Zhou You-Ya, Yan Xiu-Ping, Kim Ki-Nam, Wang Shan-Wei, Liu Ming-Guang
Key Laboratory of Functional Polymer Materials, The Ministry of Education of China, Research Center for Analytical Sciences, College of Chemistry, Nankai University, Tianjin 300071, China.
J Chromatogr A. 2006 May 26;1116(1-2):172-8. doi: 10.1016/j.chroma.2006.03.061. Epub 2006 Apr 17.
The copper(II) isonicotinate (Cu(4-C5H4N-COO)2(H2O)4) coordination polymer was prepared, characterized and explored as sorbent for flow injection solid-phase extraction on-line coupled with high-performance liquid chromatography (HPLC) for determination of trace polycyclic aromatic hydrocarbons (PAHs) in environmental matrices. Naphthalene, phenanthrene, anthracene, fluoranthene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene and benzo(ghi)perylene with various shape, size and hydrophobicity were used as model analytes. The porosity of the coordination polymer allows these guest PAHs molecules to diffuse into the buck structure, and the shape and size of the pores lead to shape- and size-selectivity over the guests. The precolumn packed with the coordination polymer was shown to be promising for solid-phase extraction of PAHs in environmental samples with subsequent HPLC separation and UV detection. With extraction of 50 ml of sample solution, the enhancement factors for the PAHs studied ranged from 200 to 2337, depending on the shape, size and hydrophobic property of the PAHs. The detection limits (S/N = 3) of 2-14 ng l(-1) and the sample throughput of 3 samples h(-1) were obtained. The developed method was applied to the determination of trace PAHs in a certified reference material (coal fly ash) and local water samples.
制备并表征了异烟酸铜(II)(Cu(4-C5H4N-COO)2(H2O)4)配位聚合物,并将其用作流动注射固相萃取吸附剂,与高效液相色谱(HPLC)在线联用,用于测定环境基质中的痕量多环芳烃(PAHs)。以萘、菲、蒽、荧蒽、苯并(b)荧蒽、苯并(k)荧蒽、苯并(a)芘和苯并(ghi)苝等具有不同形状、尺寸和疏水性的物质作为模型分析物。配位聚合物的孔隙率使这些客体PAHs分子能够扩散到主体结构中,且孔隙的形状和尺寸导致对客体具有形状和尺寸选择性。装有配位聚合物的预柱被证明在对环境样品中的PAHs进行固相萃取,随后进行HPLC分离和紫外检测方面具有前景。萃取50 ml样品溶液时,所研究PAHs的增强因子在200至2337之间,这取决于PAHs的形状、尺寸和疏水性质。获得了2 - 14 ng l(-1)的检测限(S/N = 3)和每小时3个样品的进样量。所建立的方法应用于测定有证标准物质(粉煤灰)和当地水样中的痕量PAHs。