Determination of Sulfur in Grape and Apricot Samples Using High-resolution Continuum Source Electrothermal Molecular Absorption Spectrometry.

The determination of sulfur in apricot and grape samples was performed by using high-resolution continuum source electrothermal molecular absorption spectrometry based on vaporization of the carbon monosulfide (CS) molecule. CS forms in the gas phase without the addition of any molecule-forming element, since graphite cuvette contains plenty of carbon as well as food samples. A mixture of 15 µg Pd + 10 µg Mg was used in solution as the chemical modifier. The best sensitivity was obtained at 900°C of the pyrolysis temperature with a K2SO4 calibration solution. The calibration plot drew a linear path between 50 and 1600 ng of sulfur, and the limit of detection was found to be 23 ng. The accuracy of the method was confirmed with the use of a standard reference material (Rice Flour, NIST SRM 1568a). The sulfur content in chemically dried apricot samples (1987 ± 45 mg/kg) was determined to be higher than that of apricot samples dried under sunshine.

Determination of TNT and its metabolites in water samples by voltammetric techniques.

Square-wave voltammetry with the hanging drop mercury electrode as the working electrode was used for the determination of ultratraces of explosives in aqueous solution. It was shown that the strong pressure dependence of the pneumatically controlled multimode electrode system of a conventional Metrohm apparatus could be compensated by an additional pressure regulation, through which the pressure variations could be decreased when switching from deaeration to the static measurements. By using square-wave voltammetry with this electrode system after this modification the limits of detection for 2,4,6-trinitrotoluene (TNT) and other TNT-metabolites could be decreased down to 0.2 microg L(-1) when using a measurement time of 6 min. Also a simultaneous determination of TNT and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) was shown to be possible over a wide linear range and the detection limits then were 2.2 microg L(-1) for TNT and 25 microg L(-1) for RDX. By applying the highly stable and adjustable pressure as mentioned before, the calibrations could be kept stable over a period of up to 1 week.

The development of microplasmas for spectrochemical analysis.

Miniaturized microwave, high-frequency, and dc-powered microplasmas are discussed, with emphasis on the state-of-the-art and development trends. Specific atomic emission sources discussed include the microstrip microwave plasma operated in argon and helium at ca 10-30 W and below 1 L min(-1) gas at atmospheric pressure, the capacitively coupled microplasma, operated at 13.56 MHz, 5-25 W, and 17-150 mL min(-1) helium, the miniaturized inductively coupled plasma operated at several watts and reduced pressure, and dc glow-discharge plasmas on a chip, including a barrier-layer discharge as atom reservoir for atomic absorption spectrometry. Diagnostics for these sources are discussed and some of their figures of merit are compared with those of conventional sources. Current possibilities for introduction of gaseous samples are reported and scope for further development and outlook are both discussed.