Abstract
The least-squares background correction (LSBC) and internal standardization procedures were combined to eliminate spectral interferences caused by the CS molecular band (251.602 nm) and transport effects for determining Si in sulfuric acid digests of lubricant oil by high-resolution continuum source flame atomic absorption spectrometry. Aluminum, Ba, Ti, V, and W were tested as internal standard (IS) candidates, and W provided the best results. For absorbance measurements of solutions containing 0.5–5.0 mg L−1 Si in the presence of 25 mg L−1 W (at the wavelength integrated absorbance equivalent to 3 pixels), the correlation coefficient for the ratio of absorbance of Si to absorbance of W vs. analyte concentration was 0.9978. Fluctuations in analytical signals due to variations in sulfuric acid concentrations or acetylene/nitrous oxide flow-rate ratios were corrected by using this calibration plot. Relative standard deviations varied from 1.9 to 7.2% and 2.1 to 5.4% (n = 12) with and without LSBC/IS, respectively. Recoveries for samples spiked with 2.0 mg L−1 Si in 5.0% (v/v) sulfuric acid were within the 72.5–82.5% and 94.0–99.0% ranges without correction and by LSBC associated with internal standardization procedure, respectively. Accuracy of the proposed method was checked for the determination of Si in commercial lubricant oils and results obtained with internal standardization were better than those without correction.
Acknowledgments
The authors thank the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) for financially supporting this work and for a fellowship to S. R. Oliveira. They are also grateful to the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) for grants and fellowships to J. L. Raposo, Jr., J. A. Nóbrega, and J. A. Gomes Neto.
Notes
*All solutions contain 25.0 mg L−1 W as internal standard.
*NIST 1848 Lubricant Oil Additive Package. Certified value: 0.005 ± 0.0002% (m/m) or 0.60 mg L−1 (600 mg of SRM digested and diluted to 50 mL).