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Halogen oxides analysis

Principles and Characteristics Combustion analysis is used primarily to determine C, H, N, O, S, P, and halogens in a variety of organic and inorganic materials (gas, liquid or solid) at trace to per cent level, e.g. for the determination of organic-bound halogens in epoxy moulding resins, halogenated hydrocarbons, brominated resins, phosphorous in flame-retardant materials, etc. Sample quantities are dependent upon the concentration level of the analyte. A precise assay can usually be obtained with a few mg of material. Combustions are performed under controlled conditions, usually in the presence of catalysts. Oxidative combustions are most common. The element of interest is converted into a reaction product, which is then determined by techniques such as GC, IC, ion-selective electrode, titrime-try, or colorimetric measurement. Various combustion techniques are commonly used. [Pg.595]

The (EDT-TTF-I)2Br salt described above [36] and the 1 1 (TTFI4)I salt reported by Gompper [51] were the only structurally characterized salts with simple halide anions until Imakubo recently described an extensive series of Cl" and Br" salts from several ortho-diiodo tetrathiafulvalene, tetraselena-fulvalene and dithiadiselenafulvalene derivatives (Scheme 8) [62], The X-ray crystal structure analysis of the nine salts described there show a variety of halogen bonded motifs, demonstrating the adaptability of the supramolecu-lar interactions to other structural requirements imposed by the nature of the heteroatoms (O, S, Se) in the TTF frame. Indeed, in (EDT-TTF-l2)2X-(H20)2 (X = Cl, Br), a bimolecular motif (Fig. 6) associates two partially oxidized EDT-TTF-I2 molecules with one Br" anion and one water molecule. [Pg.202]

Digestion of organic material is classified as either dry ashing, when the procedure does not include liquid, or wet ashing, when liquid is used. Occasionally, fusion with Na202 (called Parr oxidation) or alkali metals may be carried out in a sealed bomb. Section 27-4 discussed combustion analysis, in which C, H, N, S, and halogens are measured. [Pg.654]

This compound is of interest not only in analysis, but because by limited oxidation with the halogens it yields a unipositive ion containing tnvalent... [Pg.1073]

Schmidt KH, Flan P, Bartels DM (1995) Radiolytic yields of the hydrated electron from transient conductivity improved calculation of the hydrated electron diffusion coefficient and analysis of some diffusion-limited (e )aq reaction rates. J Phys Chem 99 10530-10539 Schoneich C, Aced A, Asmus K-D (1991) Halogenated peroxyl radicals as two-electron-transfer agents. Oxidation of organic sulfides to sulfoxides. J Am Chem Soc 113 375-376 Schuchmann Fl-P, von Sonntag C (1981) Photolysis at 185 nm of dimethyl ether in aqueous solution Involvement of the hydroxymethyl radical. J Photochem 16 289-295 Schuchmann Fl-P, von Sonntag C (1984) Methylperoxyl radicals a study ofthey-radiolysis of methane in oxygenated aqueous solutions. Z Naturforsch 39b 217-221 Schuchmann Fl-P, von Sonntag C (1997) Heteroatom peroxyl radicals. In Alfassi ZB (ed) Peroxyl radicals. Wiley, Chichester, pp 439-455... [Pg.192]


See other pages where Halogen oxides analysis is mentioned: [Pg.459]    [Pg.428]    [Pg.33]    [Pg.243]    [Pg.1962]    [Pg.5301]    [Pg.354]    [Pg.788]    [Pg.38]    [Pg.479]    [Pg.223]    [Pg.452]    [Pg.597]    [Pg.52]    [Pg.559]    [Pg.78]    [Pg.205]    [Pg.477]    [Pg.166]    [Pg.193]    [Pg.258]    [Pg.411]    [Pg.434]    [Pg.389]    [Pg.136]    [Pg.357]    [Pg.166]    [Pg.456]    [Pg.688]    [Pg.1068]    [Pg.782]    [Pg.808]    [Pg.340]    [Pg.63]    [Pg.393]    [Pg.89]   
See also in sourсe #XX -- [ Pg.471 ]




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1-oxide halogenation

Halogen oxidants

Halogenation oxidation

Halogens analysis

Halogens oxides

Halogens oxidizers

Oxidation analysis

Oxidation halogens

Oxidative halogenation

Oxide Analyses

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