Department of Analytical Chemistry, Facultad de Ciencias. Edificio Anexo Marie Curie, Campus de Rabanales, 14071 Córdoba, Spain.
Anal Chem. 2009 Nov 1;81(21):9012-20. doi: 10.1021/ac9016264.
In this work, magnetic nanoparticles (MNPs) coated with hemimicelles of alkyl (C(10)-C(18)) carboxylates, which have traditionally been used to prepare ferrofluids for technological applications, were used for the first time to extract organic contaminants from environmental water samples. The nanoparticles were coated by following a simple, rapid procedure (30 min at 85 degrees C) that uses commercially available magnetite of 20-30 nm mean particle diameter. The strong chemical bonding between the surfactant and magnetite relative to the electrostatic forces involved in conventional hemimicelle-based sorbents precludes leaching of the surfactant and facilitates its reuse and the obtainment of surfactant-free extracts. Tetradecanoate hemimicelles were used here to extract carcinogenic polycyclic aromatic hydrocarbons (CPAHs) prior to analysis by liquid chromatography (using a C(18) Supelcosil LC-PAH column and a gradient elution program with water and acetonitrile) and fluorescence detection. The procedure involved stirring filtered aqueous samples (350 mL) with 200 mg of tetradecanoate-coated MNPs for 15 min, isolating the sorbent with a Nd-Fe-B magnet and eluting the CPAHs with a mixture of acetonitrile and tetrahydrofuran. The extraction efficiency was not influenced by salt concentrations up to 1 M and pH values over the range 2.5-9. The preconcentration factor was 116. No cleanup of the extracts was needed, and the method proved matrix-independent. The limits of quantitation thus obtained, 0.2-0.5 ng L(-1), meet the stringent water quality requirements established by the recently amended European Water Framework Directive 2000/60/EC and also the U.S. EPA for the determination of CPAHs in surface and ground waters. The proposed method was successfully applied to the determination of these pollutants in surface and ground environmental water samples collected from various places in southern Spain. Recoveries from samples spiked with CPAHs at concentrations of 1-10 ng L(-1) ranged from 85 to 94% and relative standard deviations from 1 to 7%. CPAHs were only present in the sample from the Navallana reservoir, at concentrations over the range 0.42-0.96 ng L(-1).
在这项工作中,首次使用传统上用于制备用于技术应用的铁磁流体的烷基(C(10)-C(18))羧酸的半胶束涂覆的磁性纳米粒子(MNPs)从环境水样中提取有机污染物。纳米粒子是通过以下简单,快速的程序(85°C 下 30 分钟)进行涂覆的,该程序使用商业上可获得的平均粒径为 20-30nm 的磁铁矿。与传统的基于半胶束的吸附剂中涉及的静电相比,表面活性剂与磁铁矿之间的强化学键防止了表面活性剂的浸出,并促进了其重复使用和获得无表面活性剂的提取物。十四烷酸半胶束用于在此之前分析之前提取致癌多环芳烃(CPAHs)通过液相色谱法(使用 C(18)Supelcosil LC-PAH 柱和水和乙腈的梯度洗脱程序)和荧光检测。该程序涉及用 200mg 十四烷酸涂覆的 MNPs 将过滤后的水样(350mL)搅拌 15min,用 Nd-Fe-B 磁铁分离吸附剂,并用乙腈和四氢呋喃的混合物洗脱 CPAHs。萃取效率不受盐浓度高达 1M 和 pH 值在 2.5-9 范围内的影响。预浓缩因子为 116.无需对提取物进行净化,并且该方法证明与基质无关。因此,定量限为 0.2-0.5ng L(-1),满足最近修订的欧洲水框架指令 2000/60/EC 和美国环保署规定的地表水和地下水 CPHA 的严格水质要求。该方法成功地应用于从西班牙南部不同地点采集的地表水和地下水环境水样中这些污染物的测定。从浓度为 1-10ng L(-1)的 CPHA 加标样品中回收的范围为 85-94%,相对标准偏差为 1-7%。仅在纳瓦拉纳水库的水样中存在 CPHA,浓度在 0.42-0.96ng L(-1)范围内。