Zhan Nan, Guo Feng, Zhu Shuai, Rao Zhu
The Key Laboratory of Eco-Geochemistry, Ministry of Nature Resources and National Research Center for Geoanalysis, Beijing 100037, China.
J Anal Methods Chem. 2018 Oct 1;2018:2768547. doi: 10.1155/2018/2768547. eCollection 2018.
Short-chain chlorinated paraffins (SCCPs) are a new type of persistent organic pollutants. In this work, a simple and effective method involving headspace solid-phase microextraction (HS-SPME) and comprehensive two-dimensional gas chromatography time-of-flight mass spectrometry (GC × GC-TOF-MS) was developed and optimized for the determination of trace SCCPs in water samples. The key parameters related to extraction and separation efficiency were systematically optimized. The SCCP congener groups were best resolved using an Rxi-5Sil MS (30 m × 0.25 mm × 0.25 m) column followed by an Rxi-17Sil MS (1.0 m × 0.15 mm × 0.15 m) column; the optimum extraction conditions were achieved with a 100 m polydimethylsiloxane SPME fiber, when a 10 mL water sample added with 3.6 g sodium chloride was incubated for 15 min at 90°C and then extracted during 60 min at 90°C and desorption at 260°C for 2 min. The proposed method showed good linearity in the concentration range of 0.2-20.0 g/L with the determination coefficient greater than 0.995. The detection and quantification limits ranged from 0.06 to 0.13 g/L and 0.18 to 0.40 g/L, respectively, which are sufficient to meet the regulatory detection limits as set by most environmental regulations. The accuracy and precision of the method was also good, where the recoveries ranged from 82.5 to 95.4%, and intra- and interday precision was within 7.2% and 14.5%, respectively. The optimized method has been applied to the determination of SCCPs in ten freshwater samples of three different types.
短链氯化石蜡(SCCPs)是一种新型持久性有机污染物。本研究开发并优化了一种简单有效的方法,该方法结合顶空固相微萃取(HS-SPME)和全二维气相色谱-飞行时间质谱(GC×GC-TOF-MS)用于测定水样中的痕量SCCPs。系统优化了与萃取和分离效率相关的关键参数。使用Rxi-5Sil MS(30 m×0.25 mm×0.25 m)色谱柱,随后使用Rxi-17Sil MS(1.0 m×0.15 mm×0.15 m)色谱柱时,SCCP同系物组得到了最佳分离;使用100 m聚二甲基硅氧烷SPME纤维实现了最佳萃取条件,将10 mL添加了3.6 g氯化钠的水样在90°C下孵育15 min,然后在90°C下萃取60 min,并在260°C下解吸2 min。所提出的方法在0.2 - 20.0 μg/L的浓度范围内具有良好的线性,测定系数大于0.995。检测限和定量限分别为0.06至0.13 μg/L和0.18至0.40 μg/L,足以满足大多数环境法规规定的检测限要求。该方法的准确度和精密度也良好,回收率在82.5%至95.4%之间,日内和日间精密度分别在7.2%和14.5%以内。该优化方法已应用于三种不同类型的十个淡水样品中SCCPs的测定。