Department of Environmental Chemistry, IDAEA-CSIC, Jordi Girona 18-26, 08034 Barcelona, Catalonia, Spain.
Mar Pollut Bull. 2010 Jan;60(1):103-12. doi: 10.1016/j.marpolbul.2009.08.028. Epub 2009 Sep 27.
A multi-residual method based on stir bar sorptive extraction coupled with thermal desorption-gas chromatography-mass spectrometry (SBSE-TD-GC-MS) has been developed to measure 49 organic pollutants (organochlorine pesticides, polycyclic aromatic hydrocarbons, polychlorinated biphenyls, polybrominated diphenyl ethers and nonylphenol) in seawater. Using 100ml of water, the method exhibited good linearity, with recoveries between 86% and 118% and relative standard deviation between 2% and 24% for almost all compounds. The method was applied to determine target contaminants in Catalonian seawater, including coastal areas, ports and desalination plant feed water. Overall individual compound levels oscillated between 0.16 and 597 ng l(-1); PAHs and nonylpenol were the compounds found at the highest concentrations. The method provided LODs between 0.011 and 2.5 ng l(-1), lower than the Environmental Quality Standards (EQS) fixed by Directive 2008/105/EC. In compliance with the directive, this method can be used as a tool to survey target compounds and is aimed at protecting coastal ecosystems from chemical pollution.
建立了一种基于搅拌棒吸附萃取结合热解吸-气相色谱-质谱联用(SBSE-TD-GC-MS)的多残留分析方法,用于测定海水中 49 种有机污染物(有机氯农药、多环芳烃、多氯联苯、多溴联苯醚和壬基酚)。该方法使用 100ml 水样,对于几乎所有化合物,方法的线性良好,回收率在 86%至 118%之间,相对标准偏差在 2%至 24%之间。该方法应用于加泰罗尼亚海水中目标污染物的测定,包括沿海地区、港口和海水淡化厂进水。总体而言,各化合物的浓度在 0.16 至 597ng/L 之间波动;多环芳烃和壬基酚的浓度最高。该方法的检出限在 0.011 至 2.5ng/L 之间,低于指令 2008/105/EC 规定的环境质量标准(EQS)。根据该指令,该方法可用作调查目标化合物的工具,旨在保护沿海生态系统免受化学污染。