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On-line liquid phase micro-extraction based on drop-in-plug sequential injection lab-at-valve platform for metal determination

机译:基于插入式顺序注入阀实验室平台的在线液相微萃取法测定金属

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摘要

A novel automatic on-line liquid phase micro-extraction method based on drop-in-plug sequential injection lab-at-valve (LAV) platform was proposed for metal preconcentration and determination. A flow-through micro-extraction chamber mounted at the selection valve was adopted without the need of sophisticated lab-on-valve components. Coupled to flame atomic absorption spectrometry (FAAS), the potential of this lab-at-valve scheme is demonstrated for trace lead determination in environmental and biological water samples. A hydrophobic complex of lead with ammonium pyrrolidine dithiocarbamate (APDC) was formed on-line and subsequently extracted into an 80 μL plug of chloroform. The extraction procedure was performed by forming micro-droplets of aqueous phase into the plug of the extractant. All critical parameters that affect the efficiency of the system were studied and optimized. The proposed method offered good performance characteristics and high preconcentration ratios. For 10mL sample consumption an enhancement factor of 125 was obtained. The detection limit was 1.8 μgL~(-1) and the precision expressed as relative standard deviation (RSD) at 50.0 μg L~(-1) of lead was 2.9%. The proposed method was evaluated by analyzing certified reference materials and applied for lead determination in natural waters and urine samples.
机译:提出了一种基于插装式顺序进样实验室(LAV)平台的在线液相自动微萃取新方法,用于金属的富集和测定。采用了安装在选择阀上的流通式微萃取室,而无需复杂的实验室阀门组件。结合火焰原子吸收光谱法(FAAS),该实验室阀门方案的潜力被证明可用于环境和生物水样品中的痕量铅测定。在线形成了铅与吡咯烷二硫代氨基甲酸铵的疏水复合物(APDC),然后将其萃取到80μL氯仿塞中。通过将水相的微滴形成到萃取剂的塞中来进行萃取程序。研究并优化了影响系统效率的所有关键参数。所提出的方法具有良好的性能特征和较高的预浓缩率。对于10mL的样品消耗,可获得125的增强因子。检出限为1.8μgL〜(-1),以50.0μgL〜(-1)铅表示的相对标准偏差(RSD)的精密度为2.9%。通过分析认证的参考物质对提出的方法进行了评估,并将其用于天然水和尿液样品中的铅测定。

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