Application of Multi-energy Calibration for Determination of Chromium and Nickel in Nickeliferous Ores by Laser-induced Breakdown Spectroscopy.

A multi-energy calibration method was applied for the determination of chromium and nickel in nickeliferous ores by laser-induced breakdown spectroscopy. For the optimization of the laser-induced breakdown spectroscopy parameters, such as laser fluence and delay time, an experimental study was conducted. The best results in terms of trueness were observed using a laser fluence and a delay time of 2500 J/cm2 and 1.1 µs, respectively. A study of sample matrix effects and the determination of emission lines for calibration and normalization of the spectra were undertaken, and appropriate values of those variables were selected for each analyte. The trueness values for chromium and nickel varied from 89 to 114% when certified reference samples (nickeliferous laterite, rock phosphate and contaminated soil) were analyzed.

Bismuth as a general internal standard for lead in atomic absorption spectrometry.

Bismuth was evaluated as internal standard for Pb determination by line source flame atomic absorption spectrometry (LS FAAS), high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS) and line source graphite furnace atomic absorption spectrometry (LS GFAAS). Analysis of samples containing different matrices indicated close relationship between Pb and Bi absorbances. Correlation coefficients of calibration curves built up by plotting A(Pb)/A(Bi)versus Pb concentration were higher than 0.9953 (FAAS) and higher than 0.9993 (GFAAS). Recoveries of Pb improved from 52-118% (without IS) to 97-109% (IS, LS FAAS); 74-231% (without IS) to 96-109% (IS, HR-CS FAAS); and 36-125% (without IS) to 96-110% (IS, LS GFAAS). The relative standard deviations (n=12) were reduced from 0.6-9.2% (without IS) to 0.3-4.3% (IS, LS FAAS); 0.7-7.7% (without IS) to 0.1-4.0% (IS, HR-CS FAAS); and 2.1-13% (without IS) to 0.4-5.9% (IS, LS GFAAS).