首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Monitoring of Polycyclic Aromatic Hydrocarbons in Water Using Headspace Solid-Phase Microextraction and Capillary Gas Chromatography
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Monitoring of Polycyclic Aromatic Hydrocarbons in Water Using Headspace Solid-Phase Microextraction and Capillary Gas Chromatography

机译:顶空固相微萃取和毛细管气相色谱法监测水中的多环芳烃

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摘要

A laboratory-made fused silica fiber coated with a porous layer of activated charcoal (PLAC) was used as a new microsolid phase in solid-phase microextraction (SPME) mode for sampling of polycyclic aromatic hydrocarbons (PAHs) from the headspace of water samples. Effects of temperature, salt addition, stirring speed, and exposure time on extraction efficiency were investigated. Extraction at 80 deg C for 30 min in the presence of 12 g NaCl at constant stirring speed yields maximum efficiency. Using the proposed microsolid phase as an efficient sampling device and capillary gas chromatography with flame ionization detection, reliable determination of these compounds at sub-parts-per-billion concentrations was achieved. The calibration graphs were linear in the range 0.1-50 ng/ml and the detection limits were 0.03-0.3 ng/ml. The proposed method was successfully applied to the determination of PAHs in environmental samples such as local municipal water.
机译:在固相微萃取(SPME)模式下,实验室制造的涂覆有活性炭多孔层(PLAC)的熔融石英纤维被用作新的微固相,用于从水样品的顶部空间取样多环芳烃(PAH)。研究了温度,加盐量,搅拌速度和暴露时间对萃取效率的影响。在12 g NaCl的存在下,以恒定的搅拌速度在80摄氏度下萃取30分钟,可获得最大的效率。使用拟议的微固相作为有效的采样装置和带有火焰离子化检测的毛细管气相色谱,可以可靠地测定十亿分之一以下浓度的这些化合物。校准曲线在0.1-50 ng / ml范围内呈线性,检出限为0.03-0.3 ng / ml。该方法成功地用于环境样品(如当地市政用水)中多环芳烃的测定。

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