Corps Ricardo Ana I, Guzmán Bernardo Francisco J, Zougagh Mohammed, Rodríguez Martín-Doimeadios Rosa C, Ríos Ángel
Environmental Sciences Institute (ICAM), Department of Analytical Chemistry and Food Technology, University of Castilla-La Mancha, Avda. Carlos III s/n, 45071, Toledo, Spain.
Regional Institute for Applied Chemistry Research, IRICA, University of Castilla-La Mancha, Avenida Camilo José Cela, No. 10, 13003, Ciudad Real, Spain.
Anal Bioanal Chem. 2017 Aug;409(21):5125-5132. doi: 10.1007/s00216-017-0459-7. Epub 2017 Jul 17.
A rapid and reliable method based on magnetic solid-phase extraction (MSPE) and ultra-high performance liquid chromatography (UHPLC-FLD) analysis was developed and validated for the quantitative determination of seven polycyclic aromatic hydrocarbons (PAHs) in water samples. Hybrid composites made up of magnetic nanoparticles (MNPs) and carbon nanotubes (CNTs) were tested as adsorbent materials. The main factors influencing the extraction yields were optimized, namely the amount and type of adsorbent in the adsorption, and the solvent, the type of energy and the time in the desorption step. The selected composite was made up of FeO and multiwalled (MW)-CNTs. The desorption was carried out with sonication probe and tetrahydrofuran (THF); this solvent makes the method directly compatible with the chromatographic mobile phase and it reduces the analysis time. Under the optimized conditions, the LODs and LOQs achieved were in the range of 0.025-0.73 and 0.04-2.4 ng mL, respectively. The calibration curves were linear (R ≥ 0.9936) over the concentration ranges from 1 to 500 ng mL. The recoveries of PAHs were from 76.4 ± 1.7 up to 106.5 ± 3.5%. The method was applied to synthetic and real (tap, dam, river and mineral) water samples with different characteristics to evaluate the performance under real conditions.
建立了一种基于磁性固相萃取(MSPE)和超高效液相色谱(UHPLC-FLD)分析的快速可靠方法,用于定量测定水样中的七种多环芳烃(PAHs)。测试了由磁性纳米颗粒(MNPs)和碳纳米管(CNTs)组成的混合复合材料作为吸附材料。优化了影响萃取产率的主要因素,即吸附过程中吸附剂的用量和类型,以及解吸步骤中的溶剂、能量类型和时间。所选复合材料由FeO和多壁(MW)-CNTs组成。使用超声探头和四氢呋喃(THF)进行解吸;这种溶剂使该方法与色谱流动相直接兼容,并减少了分析时间。在优化条件下,获得的检测限(LODs)和定量限(LOQs)分别在0.025-0.73和0.04-2.4 ng mL范围内。校准曲线在1至500 ng mL的浓度范围内呈线性(R≥0.9936)。PAHs的回收率为76.4±1.7%至106.5±3.5%。该方法应用于具有不同特性的合成水样和实际水样(自来水、坝水、河水和矿泉水),以评估实际条件下的性能。