Flow-injection hydride generation atomic absorption spectrometric study of the automated on-line pre-reduction of arsenate, methylarsonate and dimethylarsinate and high-performance liquid chromatographic separation of their l-cysteine complexes.

An automated on-line pre-reduction of arsenate, monomethylarsonate (MMA) and dimethylarsinate (DMA) using flow injection hydride generation atomic absorption spectrometry (FI-HGAAS) is feasible. The kinetics of pre-reduction and complexation depend strongly on the concentration of l-cysteine and on the temperature in the following increasing order: inorganic As(V)<DMA<MMA. Arsenate is pre-reduced/complexed within less than 50 s at 70-100 degrees C compared to 1 h at room temperature, while MMA and DMA require 1.5-2 min at 70-100 degrees C and up to 1-2 h at room temperature. The characteristic masses and concentrations for 100 mul injections are 0.01 ng and 0.1 mug l(-1) in integrated absorbance and 0.2 ng and 2 mug l(-1) in peak height measurements, and the limits of detection are ca. 0.5 ng and 5 mug l(-1), respectively. In a high-performance liquid chromatography (HPLC)-HGAAS system, the l-cysteine complexes of inorganic As(III), MMA and DMA are best separated within 7 min by HPLC on a strongly acidic cation exchange column such as Spherisorb S SCX 120x4 mm (5 mum) with a mobile phase containing 12 mmol l(-1) phosphate buffer (KH(2)PO(4)/H(3)PO(4))-2.5 mmol l(-1)l-cysteine, pH 3.3-3.5. Upon dilution to l-cysteine levels below 10 mmol l(-1), which are compatible with HPLC separations, the DMA-cysteine complex is unstable on storage. No baseline separations are possible with anion exchange and reverse phase C(18) HPLC columns. The limits of detection with 50 mul injections in peak area mode are ca. 0.5 ng and 10 mug l(-1), respectively.