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Halogen combustion 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]

Ag, Cl, and N to six-figure accuracy.1 This Nobel Prize-winning research allowed the accurate determination of atomic masses of many elements. In combustion analysis, a sample is burned in excess oxygen and products are measured. Combustion is typically used to measure C, H, N, S, and halogens in organic compounds. To measure other elements in food, organic matter is burned in a closed system, the products and ash (unburned material) are dissolved in acid or base, and measured by inductively coupled plasma with atomic emission or mass spectrometry. [Pg.629]

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]

Simple methods of chemical analysis are useful in certain cases. Qualitative chemical tests such as the Beilstein and Lassaigne tests for the presence of particular elements (e.g. halogens, nitrogen, sulphur) are of use in the identification of an unknown polymer. Combustion analysis for quantitative determination of elemental composition can be used to confirm the purity of a homopolymer and to determine the average... [Pg.221]

The chloride ion is one of the most frequently analysed by IC, e.g. following up combustion of polymers [854,855] similar analyses were reported for the bromide ion [854,855] and nitrite [855]. Analysis of polyester resins for halogens or phosphorous components may be carried out via conversion to halides and phosphates, respectively. [Pg.273]

Applications Basic methods for the determination of halogens in polymers are fusion with sodium carbonate (followed by determination of the sodium halide), oxygen flask combustion and XRF. Crompton [21] has reported fusion with sodium bicarbonate for the determination of traces of chlorine in PE (down to 5 ppm), fusion with sodium bisulfate for the analysis of titanium, iron and aluminium in low-pressure polyolefins (at 1 ppm level), and fusion with sodium peroxide for the complexometric determination using EDTA of traces of bromine in PS (down to 100ppm). Determination of halogens in plastics by ICP-MS can be achieved using a carbonate fusion procedure, but this will result in poor recoveries for a number of elements [88]. A sodium peroxide fusion-titration procedure is capable of determining total sulfur in polymers in amounts down to 500 ppm with an accuracy of 5% [89]. [Pg.605]

It is seen by examination of Table 1.11(b) that a wide variety of techniques have been employed including spectrophotometry (four determinants), combustion and wet digestion methods and inductively coupled plasma atomic emission spectrometry (three determinants each), atomic absorption spectrometry, potentiometric methods, molecular absorption spectrometry and gas chromatography (two determinants each), and flow-injection analysis and neutron activation analysis (one determinant each). Between them these techniques are capable of determining boron, halogens, total and particulate carbon, nitrogen, phosphorus, sulphur, silicon, selenium, arsenic antimony and bismuth in soils. [Pg.96]

Elemental Analysis. The acetone fractions were analyzed for C, H,- and N by an automatic analyzer. Sulfur and the halogens (i.e., Cl and Br) were analyzed by combustion and subsequent titration. The following standard compounds were used for quality assurance (QA) purposes acetanilide (C, H, N), sulfanilamide (S), p-chlorobenzoic acid (Cl), and p-bromobenzoic acid (Br). [Pg.189]

Combustion (elemental) analysis of polymeric supports has mainly been used to determine the amount of halogens, nitrogen, or sulfur present in samples of cross-linked polystyrene (see, e.g., [54]). This information can be used to estimate the loading of a support, or, for example, to verify that the displacement of a halide has proceeded to completion. In solid-phase peptide synthesis, nitrogen determination has been used to estimate the loading of the first amino acid [55]. [Pg.8]

When HPLC is used as part of the analysis, the mobile phase is typically a mixture of methanol and methyl-tert-butyl ether (i.e., 50 50, v/v), although other HPLC solvents for LC/MS using APCI (e.g., water, tetrahydrofuran) can be used. It is important to note that if combustible nonaqueous solvent systems are used, water or a halogenated solvent such as methylene chloride or chloroform should be added to the mobile phase postcolumn to suppress ignition in the ion source. In addition, the APCI source must be vented outside the laboratory and should not allow air into the ionization chamber. A scan range of m/z 300 to 1000 will include the known carotenoids and their most common esters. [Pg.879]

In the micro method of combustion, substances containing any of these elements (N, S and halogen) can be combusted in one tube by the use of the so-called Universal Filling (see section on Micro-analysis, p. 453). [Pg.448]

Analogous experiments with mixtures of identical combustion temperature containing various excess amounts of carbon monoxide showed that the flame velocity is proportional to [CO ]1/2, where [CO ] is the carbon monoxide concentration in the reaction zone. From this it follows that the chemical reaction in a flame is first order in carbon monoxide. The role of water in the combustion of carbon monoxide is well known. Analysis of available data shows that the flame velocity is proportional to [H20]1//2, i.e., the reaction is first order in water vapor content. The influence on combustion of such flegmatizers as CC14 may be ascribed to the binding of hydrogen by halogen with the formation of a molecule of HC1, which is dissociable only with difficulty. However, the latest experiments by Kokochashvili in our laboratory show that the influence of the... [Pg.173]

Other major shale constituents such as C, H, N, and S are determined by thermal decomposition and instrumental detection methods. Oxygen is determined by 14 MeV neutron activation analysis. Parr or Leco BTU bomb combustion and subsequent ion chromatographic determination is used for halogens, sulfate and nitrate. Ion chromatography is also suitable for anionic characterization of shale process waters. Two analytical procedures for oil shales should be used with caution. Kjeldahl nitrogen procedure has been found to give reproducible but considerably low results for certain oil... [Pg.478]

The next chapter reviews the reactions of free atoms and radicals which play an important role in the modeling of complex processes occurring in the polluted atmosphere and in combustion chemistry. J. Jodkowski discusses the computational models of the reaction rate theory most frequently used in the theoretical analysis of gas-phase reaction kinetics and presents examples of the reactions of reactive components of the polluted atmosphere, such as 02, NOx, OH, NH2, alkyl radicals, and halogen atoms. Kinetic parameters of the reactions under investigation are provided in an analytical form convenient for kinetic modeling studies. The presented expressions allow for a successful description of the kinetics of the reaction systems in a wide temperature range and could be used in kinetic studies of related species. [Pg.343]

Combustion of the sample in an oxygen combustion flask (Alcino et al., 1965) followed by ion chromatography is an attractive method for the analysis of sulfur in humic substances. Not only does the method require relatively little sample and provide high sensitivity, but it also allows simultaneous determination of halogens. One must be sure that sulfur is not rendered insoluble by ash constituents such as calcium. [Pg.443]


See other pages where Halogen combustion analysis is mentioned: [Pg.82]    [Pg.688]    [Pg.394]    [Pg.82]    [Pg.13]    [Pg.30]    [Pg.239]    [Pg.11]    [Pg.145]    [Pg.556]    [Pg.403]    [Pg.82]    [Pg.646]    [Pg.1908]    [Pg.35]    [Pg.596]    [Pg.166]    [Pg.115]    [Pg.445]    [Pg.277]    [Pg.348]    [Pg.782]    [Pg.103]    [Pg.381]    [Pg.75]    [Pg.175]    [Pg.216]    [Pg.218]    [Pg.15]    [Pg.72]    [Pg.1047]    [Pg.1047]    [Pg.139]    [Pg.36]    [Pg.404]   
See also in sourсe #XX -- [ Pg.162 ]




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