Margetínová Jana, Houserová-Pelcová Pavlína, Kubán Vlastimil
Department of Chemistry and Biochemistry, Mendel University of Agriculture and Forestry, Zemedelská 1, Brno CZ 613 00, Czech Republic.
Anal Chim Acta. 2008 May 19;615(2):115-23. doi: 10.1016/j.aca.2008.03.061. Epub 2008 Apr 7.
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(+)).
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)。