New approach of a transient ICP-MS measurement method for samples with high salinity

被引:20
|
作者
Hein, Christina [1 ]
Sander, Jonas Michael [1 ]
Kautenburger, Ralf [1 ]
机构
[1] Univ Saarland, Inst Inorgan Solid State Chem, Campus Dudweiler,Markt Zeile 5, D-66125 Saarbrucken, Germany
关键词
High salinity; ICP-MS; Ionic strength; Transient measurement; Europium; Uranium; RARE-EARTH-ELEMENTS; OPALINUS CLAY; MASS SPECTROMETRY; CHELATING RESIN; URANIUM; SEAWATER; SORPTION; PRECONCENTRATION; SEPARATION; WATER;
D O I
10.1016/j.talanta.2016.06.059
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In the near future it is necessary to establish a disposal for high level nuclear waste (HLW) in deep and stable geological formations. In Germany typical host rocks are salt or claystone. Suitable clay formations exist in the south and in the north of Germany. The geochemical conditions of these clay formations show a strong difference. In the northern ionic strengths of the pore water up to 5 M are observed. The determination of parameters like K-a values during sorption experiments of metal ions like uranium or europium as homologues for trivalent actinides onto clay stones are very important for long term safety analysis. The measurement of the low concentrated, not sorbed analytes commonly takes place by inductively coupled plasma mass spectrometry (ICP-MS). A direct measurement of high saline samples like seawater with more than 1% total dissolved salt content is not possible. Alternatives like sample clean up, preconcentration or strong dilution have more disadvantages than advantages for example more preparation steps or additional and expensive components. With a small modification of the ICP-MS sample introduction system and a home-made reprogramming of the autosampler a transient analysing method was developed which is suitable for measuring metal ions like europium and uranium in high saline sample matrices up to 5 M (NaCl). Comparisons at low ionic strength between the default and the transient measurement show the latter performs similarly well to the default measurement. Additionally no time consuming sample clean-up or expensive online dilution or matrix removal systems are necessary and the analysation shows a high sensitivity due to the data processing based on the peak area.
引用
收藏
页码:477 / 482
页数:6
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