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Elements chemical analysis

Hall, T. A. Chemical Element Analysis of Radioactive Mixtures in Biological Materials. Nucleonics 12, No. 3, 34 (1954). [Pg.90]

In all quantitative TG investigations, it is necessary to characterize the reactant, and this may require both chemical (elemental) analysis, together with structure determination for those solids that exhibit polymorphism (where reactivity can vary with crystal form). The reaction identified must be consistent with both mass change and compositional evidence (which also confirms the balance calibration). Several aspects of sample examination and reaction characterization that merit consideration are mentioned in the following paragraphs ... [Pg.150]

Crude oils form a continuum of chemical species from gas to the heaviest components made up of asphaltenes it is evidently out of the question, given the complexity of the mixtures, to analyze them completely. In this chapter we will introduce the techniques of fractionation used in the characterization of petroieum as well as the techniques of elemental analysis applied to the fractions obtained. [Pg.17]

Because model colloids tend to have a ratlier well defined chemical composition, elemental analysis can be used to obtain detailed infonnation, such as tlie grafted amount of polymer in tire case of sterically stabilized particles. More details about tire chemical stmcture can be obtained using NMR techniques (section B1.13). In addition, NMR... [Pg.2672]

Gases and vapors of volatile liquids can be introduced directly into a plasma flame for elemental analysis or for isotope ratio measurements. Some elements can be examined by first converting them chemically into volatile forms, as with the formation of hydrides of arsenic and tellurium. It is important that not too much analyte pass into the flame, as the extra material introduced into the plasma can cause it to become unstable or even to go out altogether, thereby compromising accuracy or continuity of measurement. [Pg.102]

The copolymer composition equation relates the r s to either the ratio [Eq. (7.15)] or the mole fraction [Eq. (7.18)] of the monomers in the feedstock and repeat units in the copolymer. To use this equation to evaluate rj and V2, the composition of a copolymer resulting from a feedstock of known composition must be measured. The composition of the feedstock itself must be known also, but we assume this poses no problems. The copolymer specimen must be obtained by proper sampling procedures, and purified of extraneous materials. Remember that monomers, initiators, and possibly solvents are involved in these reactions also, even though we have been focusing attention on the copolymer alone. The proportions of the two kinds of repeat unit in the copolymer is then determined by either chemical or physical methods. Elemental analysis has been the chemical method most widely used, although analysis for functional groups is also employed. [Pg.457]

The most commonly measured pigment properties ate elemental analysis, impurity content, crystal stmcture, particle size and shape, particle size distribution, density, and surface area. These parameters are measured so that pigments producers can better control production, and set up meaningful physical and chemical pigments specifications. Measurements of these properties ate not specific only to pigments. The techniques appHed are commonly used to characterize powders and soHd materials and the measutiag methods have been standardized ia various iadustries. [Pg.4]

Chemical Properties. Elemental analysis, impurity content, and stoichiometry are determined by chemical or iastmmental analysis. The use of iastmmental analytical methods (qv) is increasing because these ate usually faster, can be automated, and can be used to determine very small concentrations of elements (see Trace AND RESIDUE ANALYSIS). Atomic absorption spectroscopy and x-ray fluorescence methods are the most useful iastmmental techniques ia determining chemical compositions of inorganic pigments. Chemical analysis of principal components is carried out to determine pigment stoichiometry. Analysis of trace elements is important. The presence of undesirable elements, such as heavy metals, even in small amounts, can make the pigment unusable for environmental reasons. [Pg.4]

Only slightly less accurate ( 0.3—0.5%) and more versatile in scale are other titration techniques. Plutonium maybe oxidized in aqueous solution to PuO " 2 using AgO, and then reduced to Pu" " by a known excess of Fe", which is back-titrated with Ce" ". Pu" " may be titrated complexometricaHy with EDTA and a colorimetric indicator such as Arsenazo(I), even in the presence of a large excess of UO " 2- Solution spectrophotometry (Figs. 4 and 5) can be utilized if the plutonium oxidation state is known or controlled. The spectrophotometric method is very sensitive if a colored complex such as Arsenazo(III) is used. Analytically usehil absorption maxima and molar absorption coefficients ( s) are given in Table 10. Laser photoacoustic spectroscopy has been developed for both elemental analysis and speciation (oxidation state) at concentrations of lO " — 10 M (118). Chemical extraction can also be used to enhance this technique. [Pg.200]

Chain Structure. The chemical composition of poly (vinyhdene chloride) has been confirmed by various techniques, including elemental analysis, x-ray diffraction analysis, degradation studies, and in, Raman, and nmr spectroscopy. The polymer chain is made up of vinyhdene chloride units added head-to-tail ... [Pg.430]

Composition. The results of elemental analyses are almost always included among the specifications for a commercial catalyst. Depending on the accuracy desired and whether or not the catalyst can be rendered soluble without great difficulty, elemental analysis may be performed by x-ray methods, by one of the procedures based on atomic absorption, or by traditional wet-chemical methods. Erequentiy it is important to determine and report trace element components that may have an effect on catalyst performance. [Pg.196]

The chemical composition of particulate pollutants is determined in two forms specific elements, or specific compounds or ions. Knowledge of their chemical composition is useful in determining the sources of airborne particles and in understanding the fate of particles in the atmosphere. Elemental analysis yields results in terms of the individual elements present in a sample such as a given quantity of sulfur, S. From elemental analysis techniques we do not obtain direct information about the chemical form of S in a sample such as sulfate (SO/ ) or sulfide. Two nondestructive techniques used for direct elemental analysis of particulate samples are X-ray fluorescence spectroscopy (XRF) and neutron activation analysis (NAA). [Pg.205]

Light element spectroscopy for concentration, electronic, and chemical structure analysis at ultra-high lateral resolution in a TEM or STEM... [Pg.12]

Survey capability with ppm detection limits, not affected by surface charging effects complete elemental coverage survey microanalysis of contaminated areas, chemical failure analysis... [Pg.44]


See other pages where Elements chemical analysis is mentioned: [Pg.126]    [Pg.405]    [Pg.54]    [Pg.301]    [Pg.27]    [Pg.414]    [Pg.174]    [Pg.106]    [Pg.389]    [Pg.12]    [Pg.523]    [Pg.12]    [Pg.405]    [Pg.19]    [Pg.126]    [Pg.405]    [Pg.54]    [Pg.301]    [Pg.27]    [Pg.414]    [Pg.174]    [Pg.106]    [Pg.389]    [Pg.12]    [Pg.523]    [Pg.12]    [Pg.405]    [Pg.19]    [Pg.2788]    [Pg.50]    [Pg.276]    [Pg.420]    [Pg.208]    [Pg.262]    [Pg.18]    [Pg.333]    [Pg.322]    [Pg.366]    [Pg.368]    [Pg.379]    [Pg.220]    [Pg.58]    [Pg.233]    [Pg.276]    [Pg.173]    [Pg.240]    [Pg.22]    [Pg.166]   
See also in sourсe #XX -- [ Pg.301 ]




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