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Development of a method for the determination of SCCPs (short-chain chlorinated paraffins) in bivalve mollusk using Soxtec device followed by gas chromatography-triple quadrupole tandem mass spectrometry

机译:使用Soxtec器件在双氧化物 - 三重四极杆串联质谱室中使用苏克斯氏菌测定分枝软体动物中SCCPS(短链氯化链烷烃)的方法。

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摘要

Abstract Background Organochlorinated compounds are major environmental concern due to their persistence, long-range transportability and bio-accumulation. Chlorinated paraffin (CP) mixtures, especially short-chain CPs (SCCPs), are found in environmental samples at very high levels. However, information about their levels is still insufficient, mainly in marine biota. Methods This study aimed to optimize and validate a method for the determination of SCCPs (short-chain chlorinated paraffins) in bivalve mollusk using a Soxtec extractor and Gas Chromatography coupled with Mass Spectrometry in tandem GC-QqQ-MS/MS (EI). A Plackett-Burman (2^7*3/16) type III resolution factorial design was used to optimize the extraction and purification procedures, sample amount, extractant volume, boiling and rinsing times as extraction variables and alumina, acid silica gel amounts and elution volume as purification variables. Results The most influent factors were sample amount, rinsing time, extractant volume and acid silica gel amount. Further experiments were performed in order to attain the optimal values of these factors (4 g sample amount, 50 mL n-hexane-dichloromethane as extractant volume, 2 and 1.5 h boiling and rinsing times, 8 g alumina, 4 g acid silica gel (15%) and 50 mL n-hexane-dichloromethane as elution solvent). Validation of the optimized method presented recoveries higher than 90% with RSD below 10%, showing good accuracy and precision. The whole method limits of detection and quantification were 46.13 mg Kg- 1 and 153.75 mg Kg- 1, respectively. This method was successfully applied to the analysis of wild mussel samples coming from two Galician Rías. The found levels were very low compared to other marine systems, below parts per million. Conclusions The main advantages of the optimized method lie in the rapidity and the low amount of sorbents and volume of solvent used, as well as the selectivity and sensitivity of triple quadrupole MS/MS.
机译:摘要背景有机氯化的化合物是由于其持久性,远程可运输性和生物积累的主要环境问题。氯化石蜡(CP)混合物,尤其是短链CPS(SCCP),在很高的水平下发现。然而,有关其水平的信息仍然不足,主要是在海洋生物群中。方法本研究旨在使用苏克斯特·提取器和气相色谱法在串联GC-QQQ-MS / MS(EI)中的质谱和气相色谱和气相色谱法优化和验证用于测定双戊瘤中的SCCP(短链氯化石蜡)的方法。 III型分辨率设计的Plackett-Burman(2 ^ 7 * 3/16)用于优化提取和纯化程序,样品量,萃取剂体积,沸腾和冲洗时间作为提取变量和氧化铝,酸硅胶量和洗脱卷作为纯化变量。结果最多的影响因素是样品量,漂洗时间,萃取液体积和酸硅胶量。进行进一步的实验,以获得这些因素的最佳值(4g样品量,50ml正己烷 - 二氯甲烷作为萃取剂体积,2和1.5h沸腾和漂洗时间,8g氧化铝,4g酸硅胶( 15%)和50ml正己烷 - 二氯甲烷作为洗脱溶剂)。优化方法的验证呈现高于90%的回收率,RSD低于10%,呈现出良好的精度和精度。全部检测和定量限制分别为46.13mg kg-1和153.75mg kg-1。该方法成功地应用于来自两个加利西亚人Rías的野贻贝样品的分析。与其他海洋系统相比,发现的水平非常低,百万分之以下。结论优化方法的主要优点在于速度和少量吸附剂和使用的溶剂的体积,以及三重四极杆MS / MS的选择性和敏感性。

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