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2D simultaneous measurement of the oxyanions of P, V, As, Mo, Sb, W and U.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

<mark>Journal publication date</mark>04/2010
<mark>Journal</mark>Journal of Environmental Monitoring
Issue number4
Number of pages4
Pages (from-to)981-984
Publication StatusPublished
<mark>Original language</mark>English


Previous work used the sampling technique diffusive gradients in thin-films analysed by laser ablation mass spectrometry to measure sulphide, P, V and As at a microniche of reactive organic carbon in a freshwater sediment. Here we present new developments of this technique. The number of analytes has been extended and we demonstrate the technique for depth profiling of analytes in both one and two dimensions. The physical dimensions of the cell in the laser ablation unit restrict the maximum length of gel that can be analysed. We address this problem by proposing a method for obtaining better data continuity when analysing multiple segments of gel from the same probe. 13C is used as the internal standard for each gel segment. For the cross standardisation of different gel segments 58Fe signals are obtained from ablation of a small piece of standard ferrihydrite gel analysed during the same run as the sample gel. As the ferrihydrite gel is a subsection of a much larger gel (i.e. the Fe concentration is consistent for all subsection), then any difference in signal can be attributed to changes in detector sensitivity and gels across different runs and performed on different days can be standardised.