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采用固相萃取预富集后,通过高效液相色谱-原子荧光光谱联用技术对沉积物、底栖动物和河水样品中的汞进行形态分析。

Speciation analysis of mercury in sediments, zoobenthos and river water samples by high-performance liquid chromatography hyphenated to atomic fluorescence spectrometry following preconcentration by solid phase extraction.

作者信息

Margetínová Jana, Houserová-Pelcová Pavlína, Kubán Vlastimil

机构信息

Department of Chemistry and Biochemistry, Mendel University of Agriculture and Forestry, Zemedelská 1, Brno CZ 613 00, Czech Republic.

出版信息

Anal Chim Acta. 2008 May 19;615(2):115-23. doi: 10.1016/j.aca.2008.03.061. Epub 2008 Apr 7.

Abstract

A high-pressure microwave digestion was applied for microwave-assisted extraction (MAE) of mercury species from sediments and zoobenthos samples. A mixture containing 3molL(-1) HCl, 50% aqueous methanol and 0.2molL(-1) citric acid (for masking co-extracted Fe(3+)) was selected as the most suitable extraction agent. The efficiency of proposed extraction method was better than 95% with R.S.D. below 6%. A preconcentration method utilizing a "homemade" C18 solid phase extraction (SPE) microcolumns was developed to enhance sensitivity of the mercury species determination using on-column complex formation of mercury-2-mercaptophenol complexes. Methanol was chosen for counter-current elution of the retained mercury complexes achieving a preconcentration factor as much as 1000. The preconcentration method was applied for the speciation analysis of mercury in river water samples. The high-performance liquid chromatography-cold vapour atomic fluorescence spectrometric (HPLC/CV-AFS) method was used for the speciation analysis of mercury. The complete separation of four mercury species was achieved by an isocratic elution of aqueous methanol (65%/35%) on a Zorbax SB-C18 column (4.6mmx150mm, 5microm) using the same complexation reagent (2-mercaptophenol). The limits of detection were 4.3microg L(-1) for methylmercury (MeHg(+)), 1.4microg L(-1) for ethylmercury (EtHg(+)), 0.8microg L(-1) for inorganic mercury (Hg(2+)), 0.8microg L(-1) for phenylmercury (PhHg(+)).

摘要

采用高压微波消解技术,对沉积物和底栖动物样本中的汞形态进行微波辅助萃取(MAE)。选用含有3molL(-1) HCl、50%甲醇水溶液和0.2molL(-1)柠檬酸(用于掩蔽共萃取的Fe(3+))的混合液作为最合适的萃取剂。所提出的萃取方法效率高于95%,相对标准偏差低于6%。开发了一种利用“自制”C18固相萃取(SPE)微柱的预浓缩方法,以提高汞形态测定的灵敏度,该方法通过汞与2-巯基苯酚络合物的柱上络合反应来实现。选择甲醇对保留的汞络合物进行逆流洗脱,实现了高达1000的预浓缩因子。该预浓缩方法应用于河水样本中汞的形态分析。采用高效液相色谱-冷蒸气原子荧光光谱法(HPLC/CV-AFS)进行汞的形态分析。在Zorbax SB-C18柱(4.6mmx150mm,5μm)上,使用相同的络合试剂(2-巯基苯酚),通过甲醇水溶液(65%/35%)等度洗脱实现了四种汞形态的完全分离。甲基汞(MeHg(+))的检测限为4.3μg L(-1),乙基汞(EtHg(+))为1.4μg L(-1),无机汞(Hg(2+))为0.8μg L(-1),苯基汞(PhHg(+))为0.8μg L(-1)。

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