For the first time, a new method is described for the determination of scan
dium based on the cathodic adsorptive stripping of the scandium-alizarin re
d S complex onto a carbon paste electrode. The second-order derivative line
ar scan voltammograms of the complex are recorded by use of model JP-303 po
larographic analyzer from 0.0 to - 1.0 V (versus SCE). Optimum conditions a
re found to be: an acetic acid (0.36 mol l(-1))-potassium biphthalate (0.06
4 mol l(-1)) buffer solution (pH 4.0) containing 2.0 x 10(-5) mol l(-1) ali
zarin red S, a preconcentration potential of 0.0 V, a preconcentration time
of 60 s, a rest time of 10 s and a scan rate of 100 mV s(-1). The results
show that the complex can be adsorbed on the surface of a carbon paste elec
trode, yielding one peak at - 0.58 V, corresponding to the reduction of ali
zarin red S in the complex at the electrode. The detection limit is: found
to be 6.0 x 10(-10) mol l(-1) fur 3 min of preconcentration time. The linea
r range is 1.0 x 10(-9) to 4.0 x 10(-7) mol l(-1). Application of the proce
dure to the determination of scandium in the ore samples gave good results.
(C) 2001 Elsevier Science B.V. All rights reserved.