中文核心期刊

中国科技核心期刊

CSCD来源期刊

DOAJ 收录

Scopus 收录

刘静, 王丽, 曾兴宇, 张艳萍, 王旭亮. 固相萃取-气相色谱法测定海水中狄氏剂和多氯联苯[J]. 岩矿测试, 2014, 33(2): 282-286.
引用本文: 刘静, 王丽, 曾兴宇, 张艳萍, 王旭亮. 固相萃取-气相色谱法测定海水中狄氏剂和多氯联苯[J]. 岩矿测试, 2014, 33(2): 282-286.
Jing LIU, Li WANG, Xing-yu ZENG, Yan-ping ZHANG, Xu-liang WANG. Determination of Dieldrin and Polychlorinated Biphenyls in Seawater by Solid Phase Extraction and Capillary Gas Chromatography[J]. Rock and Mineral Analysis, 2014, 33(2): 282-286.
Citation: Jing LIU, Li WANG, Xing-yu ZENG, Yan-ping ZHANG, Xu-liang WANG. Determination of Dieldrin and Polychlorinated Biphenyls in Seawater by Solid Phase Extraction and Capillary Gas Chromatography[J]. Rock and Mineral Analysis, 2014, 33(2): 282-286.

固相萃取-气相色谱法测定海水中狄氏剂和多氯联苯

Determination of Dieldrin and Polychlorinated Biphenyls in Seawater by Solid Phase Extraction and Capillary Gas Chromatography

  • 摘要: 狄氏剂与多氯联苯均是海洋环境中毒性大、难降解的有机污染物,建立海水中狄氏剂与多氯联苯快速、灵敏、准确的检测方法,具有重要意义。本文采用聚苯乙烯/二乙烯基苯(Cleanert PS)固相萃取柱对海水样品中的狄氏剂与7种多氯联苯进行分离富集,建立了气相色谱-电子捕获检测器(GC-μECD)的分析方法。实验了萃取流速、洗脱液、水样盐度与pH等实验条件对萃取效率的影响,确定样品以5.0 mL/min的流速经Cleanert PS固相萃取柱富集,真空抽干后用5.0 mL丙酮洗脱,挥干洗脱液,用1.0 mL正己烷定容,在选定的色谱条件下进行分析。方法精密度(RSD)为0.9%~4.4%,与《海洋监测规范》GB 17378.4—2007的RSD指标相比,精密度良好;加标回收率为82.1%~123.9%。狄氏剂的检出限(0.0088 μg/L)低于文献的检出限(0.05 μg/L),7种多氯联苯的检出限(0.0012~0.0067 μg/L)低于文献的检出限(0.147~0.289 μg/L)。该方法适合于海水中痕量狄氏剂与多氯联苯的快速分析,具有一定的实用价值。

     

    Abstract: Dieldrin and polychlorinated biphenyls (PCBs) are toxic, organic pollutants that break down extremely slowly in the marine environment. Therefore, it is of valuable significance to establish a rapid, sensitive and accurate detection method for dieldrin and PCBs in seawater. A method has been developed for determining dieldrin and seven PCBs in seawater by Cleanert PS solid-phase extraction and capillary Gas Chromatography with an Electron Capture Detector (GC-μECD). Determination parameters, such as extracting flow rate, eluent, seawater salinity and pH and their effects for extraction efficiency are discussed. By the new method, dieldrin and seven PCBs were extracted from seawater under a flow rate of 5.0 mL/min, eluted by 5.0 mL acetone. The eluate was evaporated, and the solvent was set to 1.0 mL with hexane. The target compounds were determined by GC-μECD. The average recoveries of the method ranged from 82.1% to 123.9% with relative standard deviation (RSD) of 0.9%-4.4%. This method has a better precision compared with the RSD index (1.7%-7.7%) in the specification for marine monitoring (GB 17378.4—2007). The detection limit of dieldrin (0.0088 μg/L) is below the documentary detection limit (0.05 μg/L). Meanwhile, the detection limits of 7 kinds of PCBs range from 0.0012 to 0.0067 μg/L which are below their documentary detection limits (0.147-0.289 μg/L). The established method was qualified for rapid determination of dieldrin and PCBs in seawater samples with a good practical value.

     

/

返回文章
返回