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Fraction ranges, trace analysis

The boundaries of trace analysis are described by the definition of trace element in the IUPAC Compendium of Chemical Terminology, 2nd edition Any element having an average concentration of less than about 100 parts per million atoms and less than 100pg g As analytical techniques have become more sophisticated and detection capabilities have improved, this upper boundary of the definition of trace is now so far away from the capabilities of analysis in a number of fields that new terms such as ultratrace analysis have entered common parlance. There is no agreement, however, on the range of ultratrace analysis, and this term has no rigorous definition. In the literature, the term is used to define the presence of elements at mass fractions less than 10 6 and 10 8 (1 pg g 1 and 0.01 pg g ) ... [Pg.435]

Atomic absorption spectrometry has been applied to the analysis of over sixty elements. The technique combines speed, simplicity and versatility and has been applied to a very wide range of non-ferrous metal analyses. This review presents a cross section of applications. For the majority of applications flame atomisation is employed but where sensitivity is inadequate using direct aspiration of the sample solution a number of methods using a preconcentration stage have been described. Non-flame atomisation methods have been extensively applied to the analysis of ultra-trace levels of impurities in non-ferrous metals. The application of electrothermal atomisation, particularly to nickel-based alloys has enabled the determination of sub-part per million levels of impurities to be carried out in a fraction of the time required for the chemical separation and flame atomisation techniques. [Pg.251]

The main aim was to determine the distribution of PEO molecules between the gel and the supernatant fluid at r = 0.1, c = 0.1 M, T = 5°C for M = 18,000 (bridging) and polymer volume fractions in the range between v = 0 and v = 0.12. The corresponding neutron diffraction traces are shown in Figure 12.6a. In comparing these structural analyses with an independent analysis of the concentration of the PEO in the supernatant fluid, we established the following protocol in preparing the samples. [Pg.218]


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