In-situ separation of the matrix for the direct determination of traces ofchromium, cobalt, and nickel in titanium dioxide powder by electrothermal atomic-absorption spectrometry with slurry sampling
Xs. Zhu et al., In-situ separation of the matrix for the direct determination of traces ofchromium, cobalt, and nickel in titanium dioxide powder by electrothermal atomic-absorption spectrometry with slurry sampling, FRESEN J AN, 371(4), 2001, pp. 497-501
A novel method has been developed for the direct determination of traces of
chromium, cobalt, and nickel in TiO2 powder; it entails slurry sampling an
d electrothermal atomic-absorption spectrometry (ETAAS) with a polytetraflu
oroethylene (PTFE) slurry (6% m/v) as fluorinating reagent. The factors whi
ch could affect the vaporization of the matrix and analytes were studied in
detail; the fluorinating vaporization behavior of the analyte both in the
slurry and in solution were also investigated. Owing to the in-situ separat
ion of the matrix, the matrix influences were reduced significantly. The pr
oposed method has been applied to the direct determination of traces of chr
omium, cobalt, and nickel in high-purity TiO2 powder without chemical pretr
eatment. Under the optimum experimental conditions the detection limits of
the analytes (Cr, Co, and Ni) were 1.9 ng g(-1), 2.4 ng g(-1) and 5.4 ng g(
-1), respectively, the relative standard deviations (RSD) were 3.4% (n=6, c
=7.0 ng mL(-1)), 2.9% (n=6, c=0.70 ng mL(-1)), and 7.6% (n=6, c=4.0 ng mL(-
1)), again respectively, and the characteristic masses for Cr, Co, and Ni w
ere 8.4 pg/0.0044A, 9.3 pg/0.0044A, and 40.0 pg/0.0044A, respectively.