Aftafa Can, Pelit Füsun Okçu, Yalçinkaya Esra Evrim, Turkmen Hayati, Kapdan Ilgi, Nil Ertaş F
Ege University, Faculty of Science, Department of Chemistry, 35100 Bornova, İzmir, Turkey.
Ege University, Faculty of Science, Department of Chemistry, 35100 Bornova, İzmir, Turkey.
J Chromatogr A. 2014 Sep 26;1361:43-52. doi: 10.1016/j.chroma.2014.07.095. Epub 2014 Aug 4.
Clay material plays an important role in the transport and retention of many compounds in the soil, therefore, clay based sorbents are promising alternatives for selective sorption of organic pollutants. In the present work, different chain length ionic liquids (ILs) namely, 1-methyl-3-octyl-imidazolium bromide, 1-methyl-3-undecyl-imidazolium bromide and 1-methyl-3-octadecyl-imidazolium bromide were intercalated in the galleries of montmorillonite (MMT) clay. Then, this novel nanofiller surface was utilized in micro extraction of estrogenic hormones for the first time. A fast procedure where sonication-assisted emulsification microextraction combined with vortex assisted micro-solid phase extraction (μ-SPE) was developed for the LC-MS/MS analysis of estrone (E1), 17β-estradiol (E2), estriol (E3) and ethynylestradiol (EE2). The parameters related to the μ-SPE procedure namely; pH, sorbent amount, extraction solvent type and volume, sonication and vortex time, sample volume and salt effect on the extraction efficiency were screened by applying Plackett-Burmann design. The selected parameters were then optimized by using Box-Behnken design. The method was validated for the determination of estrogenic hormone residues in river water samples. Linear calibration plots were obtained for all hormones whose regression coefficients were larger than 0.98. RSD values were found less than 10% for three levels of concentration. LOD levels were calculated as; 0.012, 0.062, 0.018 and 0.693 ng L(-1) for E1, E2, E3 and EE2, respectively. Recovery values were calculated in the range of 86.9-97.7%. Considering large sample volumes required for attaining low limits of these hormones, present method provides an ease for analyst as 10 mL of the sample is adequate for achieving the same sensitivity.
黏土材料在土壤中许多化合物的迁移和保留过程中起着重要作用,因此,基于黏土的吸附剂是选择性吸附有机污染物的有前景的替代物。在本研究中,不同链长的离子液体(ILs),即1-甲基-3-辛基咪唑溴盐、1-甲基-3-十一烷基咪唑溴盐和1-甲基-3-十八烷基咪唑溴盐被插层到蒙脱石(MMT)黏土的层间。然后,这种新型纳米填料表面首次被用于雌激素的微萃取。开发了一种快速方法,即超声辅助乳化微萃取结合涡旋辅助微固相萃取(μ-SPE)用于雌酮(E1)、17β-雌二醇(E2)、雌三醇(E3)和乙炔雌二醇(EE2)的液相色谱-串联质谱(LC-MS/MS)分析。通过应用Plackett-Burmann设计筛选了与μ-SPE程序相关的参数,即pH、吸附剂用量、萃取溶剂类型和体积、超声和涡旋时间、样品体积以及盐对萃取效率的影响。然后使用Box-Behnken设计对选定的参数进行优化。该方法用于测定河水样品中雌激素残留的验证。所有激素均获得线性校准曲线,其回归系数大于0.98。三种浓度水平下的相对标准偏差(RSD)值均小于10%。检测限(LOD)分别计算为:E1为0.012 ng L⁻¹、E2为0.062 ng L⁻¹、E3为0.018 ng L⁻¹、EE2为0.693 ng L⁻¹。回收率计算范围为86.9 - 97.7%。考虑到要达到这些激素的低检测限需要大量样品体积,本方法为分析人员提供了便利,因为仅10 mL样品就足以实现相同的灵敏度。