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采用 Twisselmann 提取法、SPME 和 GC-MS 评估土壤中有机磷酸酯的输入源。

Application of Twisselmann extraction, SPME, and GC-MS to assess input sources for organophosphate esters into soil.

机构信息

Institute of Environmental Systems Research, University of Osnabrueck, D-49076 Osnabrueck, Germany.

出版信息

Environ Sci Technol. 2011 Mar 15;45(6):2264-9. doi: 10.1021/es103870f. Epub 2011 Feb 24.

Abstract

Although the ubiquitous distribution of organophosphate esters (OPEs) in the environment has been documented very thoroughly, data on their occurrence in soil is so far sparse. In this study, an analytical method was developed to determine six OPEs in soil. The method consists of a combination of Twisselmann extraction and solid-phase microextraction (SPME), followed by gas chromatography-mass spectrometry (GC-MS). To develop the method, spiked soil was extracted using a Twisselmann extractor after freeze-drying. The extract was evaporated to dryness, redissolved, and filtered. A volume of 7 mL was then analyzed by SPME, followed by GC-MS. The effects of different parameters on analyte recoveries during sample preparation, e.g., solvent for Twisselmann extraction, solvent for redissolving the extract, addition of copper, and filtration of the extract, were systematically investigated. Under optimum conditions, 10 g soil samples were extracted using toluene, and the extract was redissolved in methanol/water (1:14) and filtered. It was not necessary to add copper. For TnBP, TBEP, TCPP, and TCEP, recoveries ranged from 77.0% to 89.6%. Those for TPP and TDCP were much lower, at 31.5% and 42.0%, respectively (addition level 22.9-45.8 ng g(-1)). The variability of recoveries under these conditions was between 0.3 and 16.2% (n = 3). Limits of detection (LOD) were 0.002-3 ng g(-1). When ultrasonication was used in place of Twisselmann extraction in the developed method, recoveries were three to four times lower (27.4% to 30.6%), but the variability of recoveries was below 3% (n = 3). The method was applied to quantify OPEs in soil collected from the university campus in Osnabrueck (Germany). Average concentrations (n = 6) in soil samples ranged from 1.23 ng g(-1) to 4.96 ng g(-1) (dry weight) for TCPP, TPP, and TCEP. The results demonstrate for the first time that atmospheric deposition leads to soil contamination by OPEs.

摘要

尽管有机磷酸酯(OPEs)在环境中的普遍分布已得到充分证明,但迄今为止,有关其在土壤中存在的数据仍然很少。在本研究中,开发了一种用于测定土壤中六种 OPEs 的分析方法。该方法包括 Twisselmann 提取和固相微萃取(SPME)的组合,然后进行气相色谱-质谱(GC-MS)分析。为了开发该方法,在冷冻干燥后使用 Twisselmann 提取器从加标土壤中提取。将提取物蒸发至干,重新溶解并过滤。然后用 SPME 分析 7 mL 体积,再用 GC-MS 分析。系统研究了样品制备过程中不同参数对分析物回收率的影响,例如 Twisselmann 提取用溶剂、提取物的再溶解溶剂、添加铜和提取物的过滤。在最佳条件下,使用甲苯提取 10 g 土壤样品,并用甲醇/水(1:14)重新溶解提取物并过滤。无需添加铜。对于 TnBP、TBEP、TCPP 和 TCEP,回收率在 77.0%至 89.6%之间。TPP 和 TDCP 的回收率要低得多,分别为 31.5%和 42.0%(添加水平为 22.9-45.8 ng g(-1))。在这些条件下,回收率的变异性在 0.3%至 16.2%之间(n = 3)。检测限(LOD)为 0.002-3 ng g(-1)。在开发的方法中,用超声处理代替 Twisselmann 提取时,回收率低了三到四倍(27.4%至 30.6%),但回收率的变异性低于 3%(n = 3)。该方法用于定量分析奥斯纳布吕克大学校园(德国)采集的土壤中的 OPEs。土壤样品中 TCPP、TPP 和 TCEP 的平均浓度(n = 6)范围为 1.23 ng g(-1)至 4.96 ng g(-1)(干重)。结果首次表明,大气沉降导致 OPEs 污染土壤。

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