Simultaneous multielement determination of hydride- and oxoanion-forming elements in seawater by inductively coupled plasma mass spectrometry after lanthanum coprecipitation
T. Yabutani et al., Simultaneous multielement determination of hydride- and oxoanion-forming elements in seawater by inductively coupled plasma mass spectrometry after lanthanum coprecipitation, B CHEM S J, 73(4), 2000, pp. 895-901
The simultaneous multielement determination of trace elements in seawater,
especially hydride- and oxoanionforming elements, has been investigated by
inductively coupled plasma mass spectrometry with the aid of lanthanum copr
ecipitation preconcentration. The optimum pH in lanthanum coprecipitation w
as pH 9.5; at this value, trace elements were well recovered and major cons
tituents of seawater such as Na, Mg, K, and Ca were significantly reduced i
n the concentrated solutions. The recovery values obtained for V, Cr(III),
Mn, As(III), As(V), Se(IV), Y, Sn, Sb(III), Sb(V), W,Bi, and U were more th
an 85% after lanthanum coprecipitation, while Cr(VI), Se(VI), and Mo(VI) pr
ovided poor recoveries of less than 30%. The reproducibility for coprecipit
ation was within 5% as relative standard deviation. The present method was
applied to the determination of trace elements in coastal seawater referenc
e material CASS-3. The analytical values for Mn, As, V, Y,Sb, W, and U were
in fairly good agreement with the certified or literature values.