## Abstract This study describes an SPE coupled with large volume injection (LVI) analytical method for the analysis of organochlorine pesticides, BHC (α, β, Δ), aldrin, endosulfan (α, β), endrin, dieldrin, and DDT, from aqueous samples. Determination was carried out by GC with MS. The LODs of orga
Multi-residue determination of organophosphorus and organochlorine pesticides in environmental samples using solid-phase extraction with cigarette filter followed by gas chromatography–mass spectrometry
✍ Scribed by Guozhen Fang; Wen Chen; Yunping Yao; Junping Wang; Junyan Qin; Shuo Wang
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 134 KB
- Volume
- 35
- Category
- Article
- ISSN
- 1615-9306
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✦ Synopsis
Abstract
A solid‐phase extraction (SPE) method was developed to extract 14 pesticides simultaneously from environment samples using cigarette filter as the sorbent before gas chromatography‐mass spectrometry (GC‐MS) analysis. Parameters influencing the extraction efficiency, such as the sample loading flow rate, eluent and elution volume, were optimized. The optimum sample loading rate was 3 mL/min, and the retained compounds were eluted with 6 mL of eluent at 1 mL/min under vacuum. Good linearity was obtained for all the 14 pesticides (r^2^>0.99) from 0.1 to 20 μg/L for water and from 2 to 400 μg/kg for soil samples. The detection limits (signal‐to‐noise=3) of the proposed method ranged from 0.01 to 0.20 μg/L for water samples and from 0.42 to 6.95 μg/kg for soil samples. The developed method was successfully applied for determination of the analytes in real environmental samples, and the mean recoveries ranged from 76.4 to 103.7% for water samples and from 79.9 to 105.3% for soil samples with the precisions (relative standard deviation) between 2.0 and 13.6%.
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