Accounting for Interelement Interferences in Atomic Emission Spectroscopy: A Nonlinear Theory

The article describes a nonlinear theory of how the presence of third elements affects the results of analyzing the elemental composition of substances by means of atomic emission spectroscopy. The theory is based on the assumption that there is an arbitrary relationship between the intensity of the analytical line of the analyte and the concentration of impurities and alloying elements. The theory has been tested on a simulation problem using commercially available equipment (the SPAS-05 spark spectrometer). By comparing the proposed algorithm with the traditional one, which assumes that there is a linear relationship between the intensity of the analytical line of the analyte and the intensities of the spectral lines (or concentrations) in the substance, it was revealed that there is a severalfold decrease in the deviations of nominal impurity concentrations from the measured ones. The results of this study allow for reducing the number of analytical procedures used in analyzing materials that have different compositions and the same matrix element. For instance, it becomes possible to determine the composition of iron-based alloys (low-alloy and carbon steels; high-speed steels; high-alloy, and heat-resistant steels) using one calibration curve within the framework of a universal analytical method.

Analysis of Mercury in Skin Lightening Cream by Microwave Plasma Atomic Emission Spectroscopy (MP-AES)

This research aimed at developing an analysis method, which was optimized and validated to determine the content of mercury in skin lightening cream discovered in the market in Bandar Lampung, Indonesia, through the use of microwave plasma atomic emission spectroscopy (MP-AES). The optimization on the analysis method was conducted on pump rate, viewing position, and reductant concentration in order to obtain the highest mercury emission intensity, while the solution stability was optimized to know the stability of mercury in the solution. The result showed that the method developed had precision with a relative standard deviation of 2.67%, recovery value of 92.78%, and linearity with an r value of 0.993, respectively. The sensitivity of the instrument detection had a limit of analysis method detection and quantification of 0.59 and 1.98 µg/L, respectively. The results of the test of the lightening cream (8 of 16 samples) positively contained mercury in the range of 422.61–44,960.79 ng/g. Therefore the method of analysis developed may be used for routine analysis of chemicals in any cosmetics products.

Levels of selected metals in teff grain samples collected from three different areas of Ethiopia by microwave plasma-atomic emission spectroscopy

The levels of selected essential and non-essential metals in the white, red, and mixed teff grains collected from Bure, Debre Markos and Bahir Dar (Ethiopia) were determined by microwave plasma-atomic emission spectroscopy (MP-AES). After proper sample pretreatment, the powdered teff was wet digested with the acid mixture (5 mL HNO3:1 mL HClO4) at 240 oC for 2:30 h over Kjeldhal digestion block. The accuracy of the optimized procedure was evaluated by analyzing the digest of the spiked samples with a standard solution of metals, and the percentage recoveries varied from 92% to 104%. The mean concentrations of metals determined (mg/kg, dry weight) were in the ranges of Al (713-1513) > Fe (252-1195) > Ca (233-348) > Zn (69-102) > Mn (20-45) > Cu (13-15) > Pb (1.8-2.8) > Cd (0.8-1.8). In this study, Al and Cd were determined in the teff for the first time. Analysis of variance indicated no significant difference between the mean concentrations of Cu and Mn among the white teff samples, Mn among the red teff samples and Cd and Pb among the mixed teff samples, but there was a significant difference for the other studied metals among the corresponding teff samples at 95% confidence level. KEY WORDS: Teff grain, Eragrostistef (Zucc.) Trotter, Essential metals, Non-essential metals, Ethiopia Bull. Chem. Soc. Ethiop. 2020, 34(3), 449-462. DOI: https://dx.doi.org/10.4314/bcse.v34i3.2