Determination of polycyclic aromatic hydrocarbons in water using dispersive liquid-liquid microextraction-gas chromatography-mass spectrometric

Nada Abusalah Almabrouk Imrigha, M. M. Sanagi, Sarra Younes Sharef
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引用次数: 1

Abstract

For the extraction of polycyclic aromatic hydrocarbons (PAHs) from water samples, a new sample preparation approach based on dispersive liquid-liquid microextraction (DLLME) was developed. In this procedure, a water sample was injected with a mixture of carbon tetrachloride, CCl4 (extraction solvent), and acetone (disperser solvent) to generate an emulsion in which the PAHs were extracted into fine droplets of extraction solvent. The impacts of several extraction parameters were explored, including extraction solvent type, disperser solvent type, extraction solvent volume, and disperser solvent volume. For phenanthrene and fluoranthene, the calibration curve correlation coefficient (r2) was 0.9993 and 0.9973, respectively. For phenanthrene and fluoranthene, the limits of detection (LODs) were 0.0008 g/mL and 0.0006 g/mL, respectively. For phenanthrene and fluoranthene, the relative standard deviations (RSDs) were 10.69 percent and 9.72 percent, respectively. The analyte recovery rates ranged from 100.5 to 107.8%. Phenanthrene and fluoranthene were discovered in the samples.
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分散液-液微萃取-气相色谱-质谱法测定水中多环芳烃
针对水样中多环芳烃(PAHs)的提取,提出了一种基于分散液液微萃取(DLLME)的样品制备方法。该方法是在水样中注入四氯化碳、四氯化碳(萃取溶剂)和丙酮(分散剂溶剂)的混合物,形成乳状液,其中多环芳烃被萃取成萃取溶剂的细滴。考察了萃取溶剂类型、分散剂类型、萃取溶剂体积、分散剂体积等萃取参数对萃取效果的影响。菲、氟蒽的相关系数(r2)分别为0.9993和0.9973。菲和荧光蒽的检出限分别为0.0008 g/mL和0.0006 g/mL。菲和荧光蒽的相对标准偏差(rsd)分别为10.69%和9.72%。分析物回收率为100.5% ~ 107.8%。在样品中发现了菲和氟蒽。
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