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Quantitative Chemical Analysis

Anleitung zur qualitativen chemischen Analysey Bonn, 1841 tr. J. Lloyd Bullock, Elementary Instruction in Qualitative Analysisy with short intr. by Liebig, 1841 Anleitung zur quantitativen chemischen Analysey Brunswick, 1846 Instruction in Chemical Analysis Quantitative)y tr. J. L. Bullock, 1846. [Pg.318]

Instruction in Que datiee Analysis, widt short intr. by Lid>ig, 1841 AtdeiUmg zur quantitativen chemischen Analyse, Brunswidc, 1846 Instruction in Chemical Analysis (Quantitative), tr. J. L. BuUock, 1846. [Pg.173]

You will come across numerous examples of qualitative and quantitative methods in this text, most of which are routine examples of chemical analysis. It is important to remember, however, that nonroutine problems prompted analytical chemists to develop these methods. Whenever possible, we will try to place these methods in their appropriate historical context. In addition, examples of current research problems in analytical chemistry are scattered throughout the text. [Pg.5]

Presenilis, C. R. A System of Instruction in Quantitative Chemical Analysis. John Wiley and Sons New York, 1881. [Pg.10]

Chemical analysis of the metal can serve various purposes. For the determination of the metal-alloy composition, a variety of techniques has been used. In the past, wet-chemical analysis was often employed, but the significant size of the sample needed was a primary drawback. Nondestmctive, energy-dispersive x-ray fluorescence spectrometry is often used when no high precision is needed. However, this technique only allows a surface analysis, and significant surface phenomena such as preferential enrichments and depletions, which often occur in objects having a burial history, can cause serious errors. For more precise quantitative analyses samples have to be removed from below the surface to be analyzed by means of atomic absorption (82), spectrographic techniques (78,83), etc. [Pg.421]

Guidelines for Chemical Process Quantitative Pisk Analysis American Institute of Chemical Engineers, Center for Chemical Process Safety, New York, 1989. [Pg.478]

Chemical Process Quantitative Risk Analysis Process Equipment Reliability Data, with Data Tables Technical Management of Chemical Process Safety (Plant)... [Pg.103]

Chemical Analysis. Plasma oxidation and other reactions often are used to prepare samples for analysis by either wet or dry methods. Plasma excitation is commonly used with atomic emission or absorption spectroscopy for quaUtative and quantitative spectrochemical analysis (86—88). [Pg.114]

Chemical Analysis. The presence of siUcones in a sample can be ascertained quaUtatively by burning a small amount of the sample on the tip of a spatula. SiUcones bum with a characteristic sparkly flame and emit a white sooty smoke on combustion. A white ashen residue is often deposited as well. If this residue dissolves and becomes volatile when heated with hydrofluoric acid, it is most likely a siUceous residue (437). Quantitative measurement of total sihcon in a sample is often accompHshed indirectly, by converting the species to siUca or siUcate, followed by deterrnination of the heteropoly blue sihcomolybdate, which absorbs at 800 nm, using atomic spectroscopy or uv spectroscopy (438—443). Pyrolysis gc followed by mass spectroscopic detection of the pyrolysate is a particularly sensitive tool for identifying siUcones (442,443). This technique rehes on the pyrolytic conversion of siUcones to cycHcs, predominantly to [541-05-9] which is readily detected and quantified (eq. 37). [Pg.59]

X-rays provide an important suite of methods for nondestmctive quantitative spectrochemical analysis for elements of atomic number Z > 12. Spectroscopy iavolving x-ray absorption and emission (269—273) is discussed hereia. X-ray diffraction and electron spectroscopies such as Auger and electron spectroscopy for chemical analysis (esca) or x-ray photoelectron spectroscopy are discussed elsewhere (see X-raytechnology). [Pg.320]

FIGt 26-58 Nomograph to determine the downwind distance affected hy a release. Adapted from Guidelines for Chemical Process Quantitative Risk Analysis, 1989, p. 90. Used hy permission of the American Institute of Chemical Engineers.)... [Pg.2344]

A complete analysis of dense gas dispersion is much beyond the scope of this treatise. More detailed references are available (Britter and McQuaid, Workbook on the Dispersion of Dense Gases, Health and Safety Executive Report No. 17/1988, England, 1988 Lees, 1986, pp. 455 61 Hanna and Drivas, 1987 Workbook of Test Cases for Vapor Cloud Source Dispersion Models, AlChE, 1989 Guidelines for Chemical Process Quantitative Risk Analysis, 1989, pp. 96-103). [Pg.2344]

CPQRA Chemical process quantitative risk analysis... [Pg.74]

The acronym for chemical process quantitative risk analysis. It is the process of hazard identification followed by numerical evaluation of incident consequences and frequencies, and their combination into an overall measure of risk when applied to the chemical process industry. It is particularly applied to episodic events. It differs from, but is related to, a probabilistic risk analysis (PRA), a quantitative tool used in the nuclear industry... [Pg.76]


See other pages where Quantitative Chemical Analysis is mentioned: [Pg.453]    [Pg.187]    [Pg.194]    [Pg.196]    [Pg.198]    [Pg.200]    [Pg.202]    [Pg.204]    [Pg.206]    [Pg.208]    [Pg.210]    [Pg.212]    [Pg.214]    [Pg.216]    [Pg.218]    [Pg.220]    [Pg.222]    [Pg.224]    [Pg.226]    [Pg.453]    [Pg.187]    [Pg.194]    [Pg.196]    [Pg.198]    [Pg.200]    [Pg.202]    [Pg.204]    [Pg.206]    [Pg.208]    [Pg.210]    [Pg.212]    [Pg.214]    [Pg.216]    [Pg.218]    [Pg.220]    [Pg.222]    [Pg.224]    [Pg.226]    [Pg.2]    [Pg.418]    [Pg.378]    [Pg.282]    [Pg.397]    [Pg.401]    [Pg.2270]    [Pg.2305]    [Pg.2313]    [Pg.36]    [Pg.240]    [Pg.54]   
See also in sourсe #XX -- [ Pg.266 , Pg.279 , Pg.280 , Pg.289 ]




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