A procedure for the sequential determination of arsenite [As(III)] and
arsenate [As(V)] based on electrochemical detection for As(III) and s
pectrophotometric detection for As(V) following ion chromatographic se
paration was developed. The color-developing system was based on the i
on-association complex formed by heteropolymolybdoarsenic acid with bi
smuth in the presence of Triton X-100. Experimental conditions for ele
ctrochemical detection and color-developing conditions were optimized
for As(III) and As(V), respectively. The optimal applied potential for
electrochemical detection of As(III) was + 0.35 V and the wavelength
for spectrophotometric detection of As(V) was 700 nm. By using an elue
nt of 2.0 mM sodium hydrogencarbonate-5.5 mM sodium carbonate with a 1
75 mu l sample loop for ion chromatographic separation, the detection
limits, which are defined as the concentrations that give the peak int
ensity twice the baseline noise, are found to be 2.9 mu g/l for As(III
) and 13 mu g/l for As(V), respectively. The spiked waste water sample
s were analyzed and recoveries were found to be 97.5-104% for As(III)
and 93.5-103% for As(V), respectively.