Pacheco-Fernández Idaira, Najafi Ali, Pino Verónica, Anderson Jared L, Ayala Juan H, Afonso Ana M
Departamento de Química, Unidad de Química Analítica, Universidad de La Laguna (ULL), La Laguna, Tenerife 38206, Spain.
Department of Chemistry and Biochemistry, The University of Toledo, Toledo, OH 43606, USA.
Talanta. 2016 Sep 1;158:125-133. doi: 10.1016/j.talanta.2016.05.041. Epub 2016 May 14.
Several crosslinked polymeric ionic liquid (PIL)-based sorbent coatings of different nature were prepared by UV polymerization onto nitinol wires. They were evaluated in a direct-immersion solid-phase microextraction (DI-SPME) method in combination with high-performance liquid chromatography (HPLC) and diode array detection (DAD). The studied PIL coatings contained either vinyl alkyl or vinylbenzyl imidazolium-based (ViCnIm- or ViBCnIm-) IL monomers with different anions, as well as different dicationic IL crosslinkers. The analytical performance of these PIL-based SPME coatings was firstly evaluated for the extraction of a group of 10 different model analytes, including hydrocarbons and phenols, while exhaustively comparing the performance with commercial SPME fibers such as polydimethylsyloxane (PDMS), polyacrylate (PA) and polydimethylsiloxane/divinylbenzene (PDMS/DVB), and using all fibers under optimized conditions. Those fibers exhibiting a high selectivity for polar compounds were selected to carry out an analytical method for a group of 5 alkylphenols, including bisphenol-A (BPA) and nonylphenol (n-NP). Under optimum conditions, average relative recoveries of 108% and inter-day precision values (3 non-consecutive days) lower than 19% were obtained for a spiked level of 10µgL(-1). Correlations coefficients for the overall method ranged between 0.990 and 0.999, and limits of detection were down to 1µgL(-1). Tap water, river water, and bottled water were analyzed to evaluate matrix effects. Comparison with the PA fiber was also performed in terms of analytical performance. Partition coefficients (logKfs) of the alkylphenols to the SPME coating varied from 1.69 to 2.45 for the most efficient PIL-based fiber, and from 1.58 to 2.30 for the PA fiber. These results agree with those obtained by the normalized calibration slopes, pointing out the affinity of these PILs-based coatings.
通过紫外光聚合将几种不同性质的基于交联聚合物离子液体(PIL)的吸附剂涂层制备在镍钛诺丝上。采用直接浸入式固相微萃取(DI-SPME)方法结合高效液相色谱(HPLC)和二极管阵列检测(DAD)对它们进行评估。所研究的PIL涂层包含带有不同阴离子的乙烯基烷基或乙烯基苄基咪唑鎓基(ViCnIm-或ViBCnIm-)离子液体单体,以及不同的双阳离子离子液体交联剂。首先评估了这些基于PIL的SPME涂层对包括烃类和酚类在内的一组10种不同模型分析物的萃取分析性能,同时将其性能与商业SPME纤维如聚二甲基硅氧烷(PDMS)、聚丙烯酸酯(PA)和聚二甲基硅氧烷/二乙烯基苯(PDMS/DVB)进行了详尽比较,并在优化条件下使用所有纤维。选择对极性化合物具有高选择性的那些纤维,对包括双酚A(BPA)和壬基酚(n-NP)在内的一组5种烷基酚进行分析方法研究。在最佳条件下,对于10μg L⁻¹的加标水平,平均相对回收率为108%,日间精密度值(3个非连续日)低于19%。整个方法的相关系数在0.990至0.999之间,检测限低至1μg L⁻¹。对自来水、河水和瓶装水进行了分析以评估基质效应。还在分析性能方面与PA纤维进行了比较。对于最有效的基于PIL的纤维,烷基酚在SPME涂层上的分配系数(logKfs)在1.69至2.45之间,对于PA纤维则在1.58至2.30之间。这些结果与通过归一化校准斜率获得的结果一致,表明了这些基于PIL的涂层的亲和力。