Determination of arsenite, arsenate, and monomethylarsonic acid in seawater by ion-exclusion chromatography combined with inductively coupled plasma mass spectrometry using reaction cell and hydride generation techniques

This paper describes a robust and sensitive method for the determination of arsenic species in seawater by ion-exclusion liquid chromatography (LC) combined with inductively coupled plasma mass spectrometry (ICP-MS) using reaction cell and hydride generation (HG) techniques. A good separation of arsenite, arsenate, and monomethylarsonic acid was achieved using an ion-exclusion column packed with a sulfonated polystyrene resin and a dilute nitric acid at pH 2.0 as the eluent, even when a large volume, i.e. 200 μl, of seawater samples containing a large amount of matrix was repeatedly injected. Separations of the chloride ion due to the matrix and arsenic species were partially performed; however, the extensive peak of ArCl due to high content of Cl − in a sample overlapped peaks of the three arsenic species on 75As measurement by ICP-MS. This ArCl polyatomic interference was efficiently eliminated by collision of ArCl molecules with helium in an octopole reaction cell which was introduced prior to a mass spectrometer. Detection limits of the three arsenic species in a sample containing 2% Cl −, the concentration of which is comparable to that in a seawater sample, by LC–ICP-MS with the octopole reaction system (ORS), ranged from 21 to 25 pg As ml −1; these values were three–six times lower than those by LC–ICP-MS without ORS. As another technique for ArCl interference elimination, HG prior to ICP-MS was also successfully used not only to reduce the interference but also to improve the detection limits to 3.4–4.5 pg As ml −1. The developed LC–ICP–ORS–MS and LC–HG–ICP-MS were validated by analyzing a certified reference material (CRM) of seawater. In addition, no serious decrease in analytical performance of present methods was observed in the experimental periods of half a year for LC–ICP–ORS–MS and 1 year for LC–HG–ICP-MS, respectively. The latter method was successfully applied to characterize seasonal variations of three arsenic species in deep seawater and surface seawater.