32 research outputs found
Resonance ionization of sputtered atoms-progress toward a quantitative technique
The combination of RIMS and ion sputtering has been heralded as the ideal means of quantitatively probing the surface of a solid. While several laboratories have demonstrated the extreme sensitivity of combining RIMS with sputtering, less effort has been devoted to the question of accuracy. Using the SARISA instrument developed at Argonne National Laboratory, a number of well-characterized metallic
samples have been analyzed. Results from these determinations have been compared with data obtained by several other analytical methods. One significant finding is that impurity measurements down to ppb levels in metal matrices can be made quantitative by employing polycrystalline metal foils as calibration standards. This discovery substantially reduces the effort required for quantitative analysis since a single standard can be used for determining concentrations spanning nine orders of magnitude
SIMS-in depth distribution analysis in insulators with high mass resolution: P in SiO2/Si
Elemental trace analysis of surfaces and interfaces: goals, accomplishments and challenges
Determination of trace elements in human milk by inductively coupled plasma sectorfield mass spectrometry (ICP-SFMS)
The potential of high resolution inductively coupled plasma sector field mass spectrometry (ICP-SFMS) was evaluated to quantify reliably various toxic and essential elements (Al, Sc, Ti, V, Cr, Mn, Fe, Ni, Co, Cu, As, Ag, Pt, Au, Pb) in human milk and infant formulae with respect to sensitivity, spectral and non-spectral interferences, blank levels, relative stability and accuracy. Some elements of potential interest such as Ti, V, Cr, Mn, Fe, Ni, Co and As are significantly interfered by polyatomic ions and cannot be determined under routine conditions without using high mass resolution, since interference levels vary significantly with the composition of the milk matrix. A microconcentric nebuliser in combination with a membrane desolvation unit was tested with respect to signal enhancement and reduction of interferences. In general, an increase of the signal intensities up to a factor of 5 was observed, whereas not all spectral interferences can be reduced to a negligible amount (only oxide containing ions to some extent). Moreover the use of the N(2) as the make-up gas did not improve the sensitivity but led to additional N-containing polyatomic interferences (e.g., for V, Cr and Mn). The use of a torch shielded by a Pt electrode did lead to the same signal intensities both for the conventional MCN100 and the MCN6000 with membrane desolvation. The investigation of In, Re, Ru, and Rh as internal standard showed that not all elements can be corrected for matrix suppression without using an additional correction factor derived from an approximate matrix composition. A series of milk samples was investigated using the optimised analytical set-up and compared to infant milk formulae. Trace element levels in instant milk formulae are significantly influenced by the quality of tap water used for preparation
Untersuchung von Hochkonzentrationseffekten von Sb und P in Silicium durch Kombination von SIMS und TEM
Precise Sulfur Isotope Ratio Measurements in Trace Concentration of Sulfur by High Resolution Inductively Coupled Plasma Sectorfield Mass Spectrometry (HR-ICP-SMS).
Abstract not availableJRC.D-Institute for Reference Materials and Measurements (Geel