Departamento de Química Analítica, Química Física e Ingeniería Química, Universidad de Alcalá, Ctra. Madrid-Barcelona Km. 33.600, Alcalá de Henares, 28871, Madrid, Spain; Departamento de Tecnología Química y Energética, Tecnología Química y Ambiental, Tecnología Mecánica y Química Analítica, E.S.C.E.T, Universidad Rey Juan Carlos, C/ Tulipán s/n, 28933, Móstoles, Madrid, Spain.
Departamento de Tecnología Química y Energética, Tecnología Química y Ambiental, Tecnología Mecánica y Química Analítica, E.S.C.E.T, Universidad Rey Juan Carlos, C/ Tulipán s/n, 28933, Móstoles, Madrid, Spain.
J Chromatogr A. 2018 Sep 7;1566:146-157. doi: 10.1016/j.chroma.2018.06.042. Epub 2018 Jun 19.
Two novel materials based on periodic mesoporous organosilica (PMO) with cationic amine-bridged ligands, (styrylmethyl)bis(triethoxysilylpropyl)ammonium chloride (PMO-STPA) and bis(3-triethoxysilylpropyl)amine (PMO-TEPA), were synthesized in this work to obtain materials with reverse-phase/strong anionic exchange mixed-mode or strong anionic exchange retention mechanism, respectively. The resulting materials were comprehensively characterized and showed functionalization with cationic amine-bridged ligands, and values of surface areas characteristic of mesoporous materials (higher than 100m/g). These materials were evaluated for the off-line solid-phase extraction (SPE) of a mixture of six phenoxy acid herbicides (fenoprop, mecoprop, dichlorprop, 2-(4-chlorophenoxy)propionic acid (4-CPPA), 2-(3-chlorophenoxy)propionic acid (3-CPPA), 2-phenoxypropionic acid (2-PPA)) from water samples previous to their analysis by CE with diode-array detection using a dual chiral selector system (20mM of heptakis(2,3,6-tri-O-methyl)-β-CD (TM-β-CD) and 7mM of (2-hydroxypropyl)-β-CD (HP-β-CD) dissolved in 50mM phosphate buffer, pH 7.0) which enabled the simultaneous enantiomeric separation of the six phenoxy acid herbicides in 11min. SPE parameters were optimized and recoveries obtained for PMO-STPA and PMO-TEPA sorbents were compared. Under the optimized conditions, it was demonstrated that using 100mg of PMO-STPA sorbent, a maximum preconcentration factor (PF) of 1500 was achieved with 750mL of standard solution, allowing recoveries between 75.5 and 112.2%, with good repeatability (RSD=1.9-8.7%, n=6). Analytical characteristics of the method were evaluated in terms of precision, linearity and accuracy with method quantitation limits (MQL) between 0.4 and 14.3μg/L. The developed method was applied to the analysis of river samples and effluents from wastewater treatment plants, with recoveries ranging from 78.3 to 107.5%.
本文合成了两种基于周期性介孔有机硅(PMO)的新型材料,(苯乙烯基)双(三乙氧基硅基丙基)氯化铵(PMO-STPA)和双(3-三乙氧基硅基丙基)胺(PMO-TEPA),分别获得具有反相/强阴离子交换混合模式或强阴离子交换保留机制的材料。对所得材料进行了综合表征,结果表明其具有阳离子桥联配体功能化,并且具有介孔材料的表面积值(高于 100m/g)。将这些材料用于离线固相萃取(SPE),从水样中萃取六种苯氧羧酸除草剂(fenoprop、mecoprop、dichlorprop、2-(4-氯苯氧基)丙酸(4-CPPA)、2-(3-氯苯氧基)丙酸(3-CPPA)、2-苯氧丙酸(2-PPA)),然后在毛细管电泳(CE)中分析,使用双手性选择剂系统(20mM 七(2,3,6-三-O-甲基)-β-CD(TM-β-CD)和 7mM(2-羟丙基)-β-CD(HP-β-CD)溶解在 50mM 磷酸盐缓冲液,pH7.0),同时实现了六种苯氧羧酸除草剂的对映体分离。优化了 SPE 参数,并比较了 PMO-STPA 和 PMO-TEPA 吸附剂的回收率。在优化条件下,使用 100mg PMO-STPA 吸附剂,在 750mL 标准溶液中可实现最大预浓缩因子(PF)为 1500,回收率在 75.5%至 112.2%之间,具有良好的重现性(RSD=1.9%-8.7%,n=6)。该方法的分析特性通过精密度、线性和准确度进行评估,方法定量限(MQL)在 0.4 至 14.3μg/L 之间。开发的方法用于河流样品和废水处理厂流出物的分析,回收率在 78.3%至 107.5%之间。