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Hemimicelles of Alkyl Carboxylates Chemisorbed onto Magnetic Nanoparticles: Study and Application to the Extraction of Carcinogenic Polycyclic Aromatic Hydrocarbons in Environmental Water Samples

机译:化学吸附到磁性纳米颗粒上的烷基羧酸半酯:在环境水样品中致癌多环芳烃的提取研究与应用

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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 deg 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 preconcen-tration 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 94percent and relative standard deviations from 1 to 7percent. CPAHs were only present in the sample from the Navallana reservoir, at concentrations over the range 0.42-0.96 ng L~(-1).
机译:在这项工作中,首次使用涂有烷基(C_(10)-C_(18))羧酸盐半胶束的磁性纳米颗粒(MNP),该磁性纳米颗粒传统上用于制备技术应用的铁磁流体。环境水样。通过遵循简单,快速的程序(在85摄氏度下30分钟)涂覆纳米颗粒,该程序使用平均粒径为20-30 nm的市售磁铁矿。表面活性剂和磁铁矿之间相对于常规半胶束基吸附剂所涉及的静电力之间的牢固化学键可防止表面活性剂的浸出,并有助于其再利用和获得不含表面活性剂的提取物。在通过液相色谱法(使用C_(18)Supelcosil LC-PAH色谱柱和水和乙腈梯度洗脱程序)进行分析之前,此处使用四十碳酸酯半胶束提取致癌的多环芳烃(CPAH)。该程序包括将过滤后的含水样品(350 mL)与200 mg十四烷酸酯涂层的MNP搅拌15分钟,用Nd-Fe-B磁体分离吸附剂,并用乙腈和四氢呋喃的混合物洗脱CPAH。提取效率不受盐浓度高达1 M和pH值在2.5-9范围内的影响。预浓缩因子为116。无需纯化提取物,该方法证明了与基质无关。这样获得的定量限为0.2-0.5 ng L〜(-1),符合最近修订的欧洲水框架指令2000/60 / EC和美国EPA所确定的严格的水质要求,用于测定地表中的CPAH。和地下水。所提出的方法已成功应用于从西班牙南部不同地方采集的地表和地面环境水样品中这些污染物的测定。浓度为1-10 ng L〜(-1)的CPAH加标样品的回收率在85%至94%之间,相对标准偏差在1%至7%之间。 CPAH仅存在于纳瓦拉纳水库的样品中,浓度范围为0.42-0.96 ng L〜(-1)。

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