Exploring the use of cork pellets in bar adsorptive microextraction for the determination of organochloride pesticides in water samples with gas chromatography/electron capture detection quantification

化学 色谱法 电子俘获探测器 气相色谱法 样品制备 萃取(化学) 奥尔德林 固相微萃取 解吸 检出限 异狄氏剂 吸附 狄氏剂 环境化学 杀虫剂 气相色谱-质谱法 质谱法 有机化学 生物 农学
作者
Júlia S. Hinz,Lucas Morés,Eduardo Carasek
出处
期刊:Journal of Chromatography A [Elsevier]
卷期号:1645: 462099-462099 被引量:15
标识
DOI:10.1016/j.chroma.2021.462099
摘要

In this study, a biosorbent material with characteristics for the adsorption of organic compounds was used for a cork pellet-based bar adsorptive microextraction technique, as a new greener alternative for the determination of organochlorine compounds. Aldrin, chlordane, dieldrin, endrin, lindane, 4,4-DDD, 4,4-DDE, 4,4-DDT, α-endosulfan and β-endosulfan were analyzed in water samples (drinking water, stream water and river water) with separation/detection by gas chromatography and electron capture detection (GC/ECD). The parameters that can affect the sample preparation efficiency such as desorption solvent and time as well as extraction time and ionic strength were evaluated by multivariate and univariate designs. Cork pellets (10 × Ø 3 mm) were used for the extraction of 15 mL of sample in the optimal conditions: 60 min of agitation with no salt added to the sample, followed by desorption of the cork pellet with 120 µL of ethyl acetate for 30 min. The bar-to-bar RSD out with five different bars showed good results with RSD ≤ 15.6%, allowing the use of simultaneous extractions. LOD and LOQ values ranged from 3 to 15 ng L−1 and 10 to 50 ng L−1 respectively, and the determination coefficients were greater than 0.9869. The target analytes were not detected in the three analyzed samples. Therefore, the recovery study was performed fortifying the water samples. Analyte recovery ranged from 48.7 – 138.2% for drinking water, 40.2 – 128.2% for stream water and 67.5 – 128.7% for river water.
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