High-performance liquid chromatographic/ion-trap mass spectrometric speciation of aquatic mercury as its pyrrolidinedithiocarbamate complexes

被引:18
作者
Houserova, Pavlina [1 ]
Matejicek, David [1 ]
Kuban, Vlastimil [1 ]
机构
[1] Mendel Univ Agr & Forestry, Dept Chem & Biochem, CZ-61300 Brno, Czech Republic
关键词
liquid chromatography; ion trap-mass spectrometry; electrospray ionization; atmospheric pressure chemical ionization; methylmercury; ethylmercury; phenylmercury; ammonium pyrrolidinedithiocarbamate; mercury-pyrrolidinedithiocarbamate; solid phase extraction;
D O I
10.1016/j.aca.2007.06.020
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
Mercury-pyrrolidinedithiocarbamate complexes are first time used for speciation of aquatic mercury with high-performance liquid chromatographic/ion trap-mass spectrometric method utilizing atmospheric pressure chemical ionization (APCI). The separation of the four mercury species was achieved in less than 5 min with a linear gradient profile of aqueous methanol from 70 up to 100% (v/v) in 4th min, isocratic elution at 100% up to 5th min and followed by a negative gradient to 70% in 6th min. The best separation was achieved on a reverse phase Zorbax Eclipse XDB C18 column (50 rum x 2.1 mm i.d., 1.8 mu m particle size). The on-column limits of detection (injection volume 1 mu L) were 370pg for methylmercury (MeHg+), 280 pg for ethylmercury (EtHg+), 250 pg for phenylmercury (PhHg+) and 90 pg for inorganic mercury (Hg2+) when the data were collected in selective ion monitoring (SIM) mode. A method of isolation and preconcentration of the mercury species using a "home-made" C18 solid phase extraction (SPE) microcolumns was developed to enhance sensitivity of the method. The preconcentration factor as much as 2500 was achieved with on-column complex formation of mercury-pyrrolidinedithiocarbamate. Methanol (100%) was chosen for elution of preconcentrated mercury species. The method was applied for the determination of mercury species in river water samples. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:242 / 250
页数:9
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