Chromatographic pre-concentration of Hg from dilute aqueous solutions for isotopic measurement by MC-ICP-MS

被引:88
作者
Chen, Jiubin [1 ]
Hintelmann, Holger [1 ]
Dimock, Brian [1 ]
机构
[1] Trent Univ, Dept Chem, Peterborough, ON K9J 7B8, Canada
关键词
MASS-INDEPENDENT FRACTIONATION; RATIO MEASUREMENTS; MERCURY ISOTOPES; SPECTROMETRY; SEPARATION; COPPER; ZN; COMPLEXES; BEHAVIOR; CU;
D O I
10.1039/c0ja00014k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Previous studies have demonstrated both mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes in the environment and the potential for their application in biochemistry and geochemistry. However, little has been reported for Hg isotope geochemistry in natural aqueous environment due to the very low concentration (1-20 ng/L). We report here, for the first time, a new protocol for directly pre-concentrating Hg using AG 1 x 4 ion-exchange resin, which allows the measurement of Hg isotope composition in freshwater samples. The protocol is validated by testing both synthetic and natural solutions of varying concentrations, and by assessing the effect of Hg recovery and organic complexants on the reproducibility and the accuracy of measured isotopic ratios. The method results in acceptable procedural blanks and quantitative yields (101% +/- 6%) in the final Hg eluates. The instrumental mass bias was corrected using modified empirical external normalization (MEEN) with Tl as internal dopant. The sensitivity of the method to the solution matrix (Hg/Tl ratio, organic matter concentration) was also evaluated. The pre-concentration and isotopic measurement protocol was applied to 16 natural water samples with Hg concentrations ranging from 0.9 ng/L to 15600 ng/L. The result showed a total variation of 2.4 parts per thousand for delta Hg-202 and evident MDF and MIF of Hg isotopes. Our study demonstrates that more research is required to fully understand the behavior of Hg isotopes in the aqueous environment.
引用
收藏
页码:1402 / 1409
页数:8
相关论文
共 48 条
[1]   The stable isotope geochemistry of copper and zinc [J].
Albarède, F .
GEOCHEMISTRY OF NON-TRADITIONAL STABLE ISOTOPES, 2004, 55 :409-427
[2]   Mass discrimination correction in multiple-collector plasma source mass spectrometry: an example using Cu and Zn isotopes [J].
Archer, C ;
Vance, D .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2004, 19 (05) :656-665
[3]   Synthesis of amine and thio chelating resins and study of their interaction with zinc(II), cadmium(II) and mercury(II) ions in their aqueous solutions [J].
Atia, AA ;
Donia, AM ;
Yousif, AM .
REACTIVE & FUNCTIONAL POLYMERS, 2003, 56 (01) :75-82
[4]   Mercury removal from water [J].
Atwood, D. A. ;
Zaman, M. K. .
RECENT DEVELOPMENTS IN MERCURY SCIENCE, 2006, 120 :163-182
[5]   Mass-dependent and -independent fractionation of Hg isotopes by photoreduction in aquatic systems [J].
Bergquist, Bridget A. ;
Blum, Joel D. .
SCIENCE, 2007, 318 (5849) :417-420
[6]   Natural Mercury Isotope Variation in Coal Deposits and Organic Soils [J].
Biswas, Abir ;
Blum, Joel D. ;
Bergquist, Bridget A. ;
Keeler, Gerald J. ;
Xie, Zhouqing .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (22) :8303-8309
[7]   Determination of mercury species in sea-water by liquid chromatography with inductively coupled plasma mass spectrometric detection [J].
Bloxham, MJ ;
Gachanja, A ;
Hill, SJ ;
Worsfold, PJ .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 1996, 11 (02) :145-148
[8]   Reporting of variations in the natural isotopic composition of mercury [J].
Blum, Joel D. ;
Bergquist, Bridget A. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2007, 388 (02) :353-359
[9]   Odd Isotope Deficits in Atmospheric Hg Measured in Lichens [J].
Carignan, Jean ;
Estrade, Nicolas ;
Sonke, Jeroen E. ;
Donard, Olivier F. X. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2009, 43 (15) :5660-5664
[10]   Application of nontraditional stable-isotope systems to the study of sources and fate of metals in the environment [J].
Chanton, J. P. ;
Powelson, D. K. ;
Abichou, T. ;
Hater, G. .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (03) :655-664