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Differences, sources

This is a monoelemental method and it requires a tight calibration per element and a different source for each one. There are however, di- or tri-atomic cathodes available. [Pg.36]

Hexane is an easy example. The variations in acentric factors are much more pronounced for heavy polar or polarizable components. It comes as no surprise that the values reported from different sources are not identical. [Pg.114]

The construction of a project cashflow requires information from a number of different sources. The principal inputs are typically -... [Pg.306]

A further advantage is the Selenium halflife of 120 days, which is 60% more when compared to iridium and a factor of approx. 4 when compared to Ytterbium. These differences turn out to be an important economical aspect when comparing the different sources, as they are a direct measure of the useful life of sources. The short halflife and the very high costs for Ytterbium sources have been the main factors for the rather low importance of Ytterbium in the full range of gamma radiography. [Pg.424]

On the other hand, the NDT service business has evolved towards a more open market, in which the prime contractor requires a transparent access to the data provided by the supplier, in order to ensure the comparison of data obtained from different sources and at different periods of time. Existing fomiats are most of the time proprietary formats released by instrument manufacturers, generally dealing with a unique NDT method and not including complementary information on the acquisition consequently, they fail to meet these requirements. [Pg.922]

We further discuss how quantities typically measured in the experiment (such as a rate constant) can be computed with the new formalism. The computations are based on stochastic path integral formulation [6]. Two different sources for stochasticity are considered. The first (A) is randomness that is part of the mathematical modeling and is built into the differential equations of motion (e.g. the Langevin equation, or Brownian dynamics). The second (B) is the uncertainty in the approximate numerical solution of the exact equations of motion. [Pg.264]

Monographs, reference books, and encyclopedias, e.g., Ullmann s Encyclopedia of Industrial Chemistry, the Kirk-Othmer Encyclopedia of Chemical Technology, or the Encyclopedia of Computational Chemistry are included in this type of literature, which is furthest from the primary literature as concerns time and content. In most cases, tertiary literature summarizes a topic with information from different sources, and additionally evaluates the contents. [Pg.239]

You have seen that measurements of heats of reaction such as heats of combustion can pro vide quantitative information concerning the relative stability of constitutional isomers (Section 2 18) and stereoisomers (Section 3 11) The box in Section 2 18 described how heats of reaction can be manipulated arithmetically to generate heats of formation (AH ) for many molecules The following material shows how two different sources of thermo chemical information heats of formation and bond dissociation energies (see Table 4 3) can reveal whether a particular reaction is exothermic or en dothermic and by how much... [Pg.174]

Two sets of data consisting of results obtained using several samples drawn from different sources. [Pg.88]

Significance testing for comparing two mean values is divided into two categories depending on the source of the data. Data are said to be unpaired when each mean is derived from the analysis of several samples drawn from the same source. Paired data are encountered when analyzing a series of samples drawn from different sources. [Pg.88]

An ion beam can be produced from a number of different sources, but for this instmment — used for biochemical examination of thermally unstable, large molecules — an atmospheric-pressure inlet such as APCl or ES would generally be used. These can be operated with liquid inlets from chromatographic columns or simply from static solutions. [Pg.402]

The values of d and n are given in Table 3 typical values for can be found in Table 4. The exponent of 0.5 on the Schmidt number (l-L /PiLj) supports the penetration theory. Further examples of empirical correlations provide partial experimental confirmation of equation 78 (3,64—68). The correlation reflecting what is probably the most comprehensive experimental basis, the Monsanto Model, also falls in this category (68,69). It is based on 545 observations from 13 different sources and may be summarized as... [Pg.36]

The properties of a botanical gum are determined by its source, the climate, season of harvest, and extraction and purification procedures. Table 6 illustrates one of the important basic properties of all gums, ie, the relationship between concentration and solution viscosity. The considerable viscosity variation observed among gums from different sources determines, in part, their uses. [Pg.433]

Hemicellulose [9034-32-6] is the least utilized component of the biomass triad comprising cellulose (qv), lignin (qv), and hemiceUulose. The term was origiaated by Schulze (1) and is used here to distinguish the nonceUulosic polysaccharides of plant cell walls from those that are not part of the wall stmcture. Confusion arises because other hemicellulose definitions based on solvent extraction are often used in the Hterature (2—4). The term polyose is used in Europe to describe these nonceUulosic polysaccharides from wood, whereas hemicellulose is used to describe the alkaline extracts from commercial pulps (4). The quantity of hemicellulose in different sources varies considerably as shown in Table 1. [Pg.29]

Table 4. A Comparison of Isolated Xylans from Different Sources... Table 4. A Comparison of Isolated Xylans from Different Sources...
Fluorescence Microscope. A useful light microscope utilizes UV light to induce fluorescence in microscopic samples (40). Because fluorescence is often the result of trace components in a given sample rather than intrinsic fluorescence of the principal component, it is useful in the crime laboratory for the comparison of particles and fibers from suspect and crime scene. Particles of the same substance from different sources almost certainly show a different group of trace elements. It is also very useful in biology where fluorescent compounds can be absorbed on (and therefore locate and identify) components of a tissue section. [Pg.334]

Serving corresponds to 236 mT. (1 cup) unless otherwise noted. Not aU. iron from different sources is equally absorbed see text. Serving corresponds to 113 g (4 oz). [Pg.383]

The nomenclature (qv) of polyamides is fraught with a variety of systematic, semisystematic, and common naming systems used variously by different sources. In North America the common practice is to call type AB or type AABB polyamides nylon-x or nylon-respectively, where x refers to the number of carbon atoms between the amide nitrogens. For type AABB polyamides, the number of carbon atoms in the diamine is indicated first, followed by the number of carbon atoms in the diacid. For example, the polyamide formed from 6-aminohexanoic acid [60-32-2] is named nylon-6 [25038-54-4], that formed from 1,6-hexanediamine [124-09-4] or hexamethylenediamine and dodecanedioic acid [693-23-2] is called nylon-6,12 [24936-74-1]. In Europe, the common practice is to use the designation "polyamide," often abbreviated PA, instead of "nylon" in the name. Thus, the two examples above become PA-6 and PA-6,12, respectively. PA is the International Union of Pure and AppHed Chemistry (lUPAC) accepted abbreviation for polyamides. [Pg.215]

Emission Standards. In order to have a nationwide basis for air pollution emission controls and to set a minimum emission limit, the EPA developed New Source Performance Standards (NSPS). The NSPS set specific poUutant emission limits or describe the best available control technology (BACT) that should be appUed at that source. The EPA has issued NSPS, which apply to new constmction as weU as to large modifications, for many different sources. Sources in the chemical industry include the foUowing. [Pg.77]

Chemical Composition. Wool wax is a complex mixture of esters of water-soluble alcohols (168) and higher fatty acids (169) with a small proportion (ca 0.5%) of hydrocarbons (170). A substantial effort has been made to identify the various components, but results are compHcated by the fact that different workers use wool waxes from different sources and employ different analytical techniques. Nevertheless, significant progress has been made, and it is possible to give approximate percentages of the various components. The wool-wax acids (Table 9) are predominantiy alkanoic, a-hydroxy, and CO-hydroxy acids. Each group contains normal, iso, and anteiso series of various chain length, and nearly all the acids are saturated. [Pg.354]

Alternatively, instabiUty or dissociation constants are sometimes used to describe compounds, and caution is necessary when comparing values from different sources. [Pg.168]

Designing an experiment is like designing a product. Every product serves a purpose so should every experiment. This purpose must be clearly defined at the outset. It may, for example, be to optimize a process, to estimate the probabiUty that a component operates properly under a given stress for a specified number of years, to evaluate the relative effects on product performance of different sources of manufacturing and end use variabiUty, or to determine whether a new process is superior to an existing one. An understanding of this purpose is important in developing an appropriate experimental plan. [Pg.519]

The effective friction loss, or gas-phase contacting power, is easily determined by direct measurements. However, the liquid-phase contacting power, supplied from the stream of scrubbing liquid, and the mechanical contacting power, supplied by a mechanically driven rotor, are not direc tly measurable the theoretical power inputs can be estimated, but the portions of these quantities effectively converted to contac ting power can only be inferred from comparison with gas-phase contacting power. Such data as are available indicate that the contributions or contacting power from different sources are directly additive in their relation to scrubber performance. [Pg.1592]

The choice of shipping in package or bulk depends on market requirements and economics. Produces from different sources that tend to have the same characteristics (appearance, quahty, price) are usually offered in bulk form. Those tending to be specialties, while sometimes offered in small bulk units, usu y are sold in packages. Many products are sold in both ways. A comparison of the costs of typical package and bulk units is given in Table 21-17. [Pg.1980]

Fuel specifications from different sources may differ in test limits on sulfur, density, etc., but the same general categories are recognized worldwide kerosene-type vaporizing fuel, distillate (or gas ou ) for atomizing burners, and more viscous blends and residuals for commerce and heavy industry. Typical specifications are as follows. [Pg.2362]


See other pages where Differences, sources is mentioned: [Pg.252]    [Pg.170]    [Pg.489]    [Pg.45]    [Pg.616]    [Pg.776]    [Pg.351]    [Pg.373]    [Pg.445]    [Pg.155]    [Pg.368]    [Pg.241]    [Pg.431]    [Pg.30]    [Pg.394]    [Pg.34]    [Pg.427]    [Pg.95]    [Pg.368]    [Pg.178]    [Pg.209]    [Pg.241]    [Pg.387]    [Pg.396]    [Pg.9]   


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From different sources biological activity

From different sources physicochemical parameters

Germ oils from different sources

Glycosaminoglycans from different sources

Glycosidases from different sources

Heparin from different sources

Methane emissions from different sources recalculated for carbon equivalent

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Potential difference source

The Reversed Uptake of Oxygen and Its Different Sources

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