Silicon determination via a SiO rotational line using high-resolution graphite furnace molecular absorption spectrometry: A straightforward approach for the analysis of solid samples prepared as suspensions

• Published in: Spectrochimica acta. Part B: Atomic spectroscopy 2021-09, Vol.183, p.106266, Article 106266
• Main Authors: Enders, Michele S.P., Coelho Junior, Gilberto S., Pires, Leticia Z., Borges, Daniel L.G.
• Format: Article
• Language: English
• Subjects: Absorption; Absorption spectroscopy; Accuracy; Acidification; Calibration; Catalysts; Gabbro; Geological samples; Graphite; High resolution; High-temperature molecular absorption; Major constituents; Molecular absorption; Petrochemical catalysts; Pyrolysis; Resolution; Resonance lines; Rocks; Rotational spectra; Scientific imaging; Sediments; Silicates; Silicon; Silicon determination; Soil; Spectrometry; Thermal decomposition; Thermal degradation; Vaporization
• ISSN: 0584-8547; 1873-3565
• DOI: 10.1016/j.sab.2021.106266

High-resolution graphite furnace molecular absorption spectrometry combined with samples prepared as suspensions were used for the quantification of Si in geological samples and in spent catalysts used for petrochemical processing. Measurements at the main Si resonance line at 251.6110 nm were proven unfeasible due to the formation of a quasi-continuous signal, which resulted in significant memory effect. An alternative was to monitor the fine rotational spectrum of SiO, which allowed memory effect-free measurements. A SiO rotational line centered at 231.9373 nm was selected to carry out quantitative analysis of Si at high percent concentrations in a variety of solid samples. Pyrolysis and vaporization temperatures were evaluated and optimized as 800 °C and 2400 °C, respectively, without the need to use a chemical modifier. Attempts to produce SiO molecules from acidified aqueous standards containing Si were unsuccessful, as the molecule could only be produced from solid samples, likely due to the formation mechanism that involves thermal decomposition of silicates. Hence, solid samples were prepared as suspensions in 0.14 mol L−1 HNO3. Calibration was performed using a series of suspensions prepared from a gabbro rock certified reference material (CRM), resulting in a limit of detection of 0.5% (m/m). The accuracy of the method was attested by the analysis of several CRM, including rocks, soils and sediments. Solid spent petrochemical catalyst samples were also analyzed and 97–114% recovery was obtained by spiking the catalyst suspensions with a CRM. The good accuracy demonstrated that the formation of SiO is free from matrix effects and highly efficient under the adopted conditions. Overall, the method was proven accurate and consists on a simple and fast alternative to determine Si in silicate-rich samples. [Display omitted] •Gas-phase SiO was produced from vaporization of silicate-based samples.•SiO molecular absorption was used for the first time to determine high levels of Si.•Interference-free quantification was proven feasible, using a CRM for calibration.•SiO was produced in the gas phase, regardless of the nature of the sample.•Samples were prepared as aqueous suspensions, resulting in high sample throughput.