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加压亚临界水萃取结合搅拌棒吸附萃取用于分析土壤中有机氯农药和氯苯的方法开发

Development of pressurized subcritical water extraction combined with stir bar sorptive extraction for the analysis of organochlorine pesticides and chlorobenzenes in soils.

作者信息

Rodil Rosario, Popp Peter

机构信息

Department of Analytical Chemistry, UFZ-Centre for Environmental Research, Germany.

出版信息

J Chromatogr A. 2006 Aug 18;1124(1-2):82-90. doi: 10.1016/j.chroma.2006.05.028.

DOI:10.1016/j.chroma.2006.05.028
PMID:16765970
Abstract

An analytical method for the determination of several organochlorine pesticides (OCPs) like hexachlorocyclohexanes (HCHs), cyclodiene derivates (dieldrin, aldrin, endrin, heptachlor, heptachlor epoxide, endrin aldehyde, endosulfan and ensodulfan sulphate) and DDX compounds (p,p'-DDE, p,p'-DDD and p,p'-DDT) as well as chlorobenzenes in soils has been developed. The procedure is based on pressurized subcritical water extraction (PSWE) followed by stir bar sorptive extraction (SBSE) and subsequent thermodesorption-gas chromatography/mass spectrometry analysis. Significant PSWE and SBSE parameters were optimized using spiked soil and water samples. For the PSWE of the organochlorine compounds, water modified with acetonitrile as the extraction solvent, at an extraction temperature of 120 degrees C, and three cycles of 10 min extraction proved to be optimal. Under optimized conditions, the figures of merit, such as precision, accuracy and detection limits were evaluated. The detection limits obtained for soil samples were in the range 0.002-4.7 ng/g. Recoveries between 4.1 and 85.2% were achieved from samples spiked at a concentration level of 25-155 ng/g. The main advantages of this method are the avoidance of clean-up and concentration procedures as well as the significant reduction of the required volume of organic solvents. The described method was applied to the determination of the pollutants in soil samples collected from a polluted area, the Bitterfeld region (Germany). The results obtained by PSWE-SBSE were in a good agreement with those obtained by a reference method, a conventional pressurized liquid extraction (PLE).

摘要

已开发出一种用于测定土壤中多种有机氯农药(OCPs)的分析方法,这些农药包括六氯环己烷(HCHs)、环二烯衍生物(狄氏剂、艾氏剂、异狄氏剂、七氯、环氧七氯、异狄氏醛、硫丹和硫丹硫酸盐)、滴滴涕化合物(p,p'-DDE、p,p'-DDD和p,p'-DDT)以及氯苯。该方法基于加压亚临界水萃取(PSWE),随后进行搅拌棒吸附萃取(SBSE)以及后续的热脱附-气相色谱/质谱分析。使用加标土壤和水样对重要的PSWE和SBSE参数进行了优化。对于有机氯化合物的PSWE,以乙腈改性的水作为萃取溶剂,萃取温度为120℃,三个10分钟的萃取循环被证明是最佳的。在优化条件下,对精密度、准确度和检测限等品质因数进行了评估。土壤样品的检测限在0.002 - 4.7 ng/g范围内。在浓度水平为25 - 155 ng/g的加标样品中,回收率在4.1%至85.2%之间。该方法的主要优点是避免了净化和浓缩步骤,以及显著减少了所需有机溶剂的体积。所描述的方法应用于测定从德国比特费尔德地区一个污染区域采集的土壤样品中的污染物。PSWE - SBSE获得的结果与参考方法(传统加压液体萃取(PLE))获得的结果高度一致。

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