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

Citation
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
Citations number
11
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY
ISSN journal
09370633 → ACNP
Volume
371
Issue
4
Year of publication
2001
Pages
497 - 501
Database
ISI
SICI code
0937-0633(200110)371:4<497:ISOTMF>2.0.ZU;2-P
Abstract
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.