Abstract

In this study, a reliable method based on the combination of ion molecule reaction ICP-MS and addition of a CH4 plasma modifier technique was established for the direct determination of Se in Ca-rich groundwater samples. The 80Se+ was oxidized to 80Se16O+ by O2, and detected at m/z 96. Under the optimized conditions (O2 flow rate=0.6mLmin−1 and Rpq=0.35), the new interferences of 96Mo+ and 96Zr+ could be oxidized to 96Mo16O+ and 96Zr16O+, and reduced by up to 300-fold and 457-fold. The poor sensitivity of 80Se16O+ was increased 3.6-fold by introduced 2mLmin−1 CH4 modifier to the ICP plasma. And a limit of quantification (LOQ, 10δ) of 0.06μgL−1 was obtained. The accuracy of proposed method was validated by analysis of certified reference materials of trace elements in water (SRM 1643e) and trace elements in natural water (SRM 1640a), and the determined values were in good agreement with the certified values. The proposed method was also successfully applied for the determination of trace Se in Ca-rich groundwater samples, and the spiked recoveries was in the range of 90.0%–103%.

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