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Relative masses

A mass spectrometer can measure integer relative mass with high accuracy, but the result is not nearly so informative as measurement of accurate relative mass. An example illustrates the reason. [Pg.271]

Density and Relative Density. Density is mass per unit volume and in SI is normally expressed as kilograms per cubic meter (density of water = 1000 kg/m or 1 g/cm ). The term specific gravity was formerly the accepted dimensionless value describing the ratio of the density of sohds and Hquids to the density of water at 4°C or for gases to the density of ak at standard conditions. The term specific gravity is being replaced by relative mass density, a more descriptive term. [Pg.310]

The energy difference between diazirine and diazomethane, interesting from the point of view of their isomerism, came from MS measurements (63JCP(39)3534). The appearance potentials of the CH2 ion, common to both compounds, yielded a difference in heats of formation of 125kJmor A strong peak in the mass spectrum of 3-chloro-3-methyl-diazirine (50) with relative mass 55 was ascribed to the methyldiazirinium ion (51). [Pg.204]

One manner in which size may be computed, for estimating purposes, is by employing a volumetric heat-transfer concept as used for rotary diyers. It it is assumed that contacting efficiency is in the same order as that provided by efficient lifters in a rotaiy dryer and that the velocity difference between gas and solids controls, Eq. (12-52) may be employed to estimate a volumetric heat-transfer coefficient. By assuming a duct diameter of 0.3 m (D) and a gas velocity of 23 m/s, if the solids velocity is taken as 80 percent of this speed, the velocity difference between the two would be 4.6 m/s. If the exit gas has a density of 1 kg/m, the relative mass flow rate of the gas G becomes 4.8 kg/(s m the volumetric heat-transfer coefficient is 2235 J/(m s K). This is not far different from many coefficients found in commercial installations however, it is usually not possible to predict accurately the acdual difference in velocity between gas and soRds. Furthermore, the coefficient is influenced by the sohds-to-gas loading and particle size, which control the total solids surface exposed to the gas. Therefore, the figure given is only an approximation. [Pg.1228]

The reaction center is built up from four polypeptide chains, three of which are called L, M, and H because they were thought to have light, medium, and heavy molecular masses as deduced from their electrophoretic mobility on SDS-PAGE. Subsequent amino acid sequence determinations showed, however, that the H chain is in fact the smallest with 258 amino acids, followed by the L chain with 273 amino acids. The M chain is the largest polypeptide with 323 amino acids. This discrepancy between apparent relative masses and real molecular weights illustrates the uncertainty in deducing molecular masses of membrane-bound proteins from their mobility in electrophoretic gels. [Pg.235]

A special type of substituent effect which has proved veiy valuable in the study of reaction mechanisms is the replacement of an atom by one of its isotopes. Isotopic substitution most often involves replacing protium by deuterium (or tritium) but is applicable to nuclei other than hydrogen. The quantitative differences are largest, however, for hydrogen, because its isotopes have the largest relative mass differences. Isotopic substitution usually has no effect on the qualitative chemical reactivity of the substrate, but often has an easily measured effect on the rate at which reaction occurs. Let us consider how this modification of the rate arises. Initially, the discussion will concern primary kinetic isotope effects, those in which a bond to the isotopically substituted atom is broken in the rate-determining step. We will use C—H bonds as the specific topic of discussion, but the same concepts apply for other elements. [Pg.222]

Gq /Gg is the relative mass flow of air through the curtain Gg is the mass flow of air through the aperture... [Pg.564]

Fig. 2.14. Atomic level relative mass motion is an expected consequence of plastic deformation. Dremin and Breusov [68D01] have described a conceptual model of such behavior (called a Roller Model ) to explain submicrosecond structural and chemical transformations under shock compression. Fig. 2.14. Atomic level relative mass motion is an expected consequence of plastic deformation. Dremin and Breusov [68D01] have described a conceptual model of such behavior (called a Roller Model ) to explain submicrosecond structural and chemical transformations under shock compression.
For the central PO block to serve as an effective hydrophobe, the value of n must be at least 15 the value of m in commercially manufactured poloxamers is such that the EO blocks constitute between 10-80% of the total polymer mass. The absolute and relative masses of the hydrophilic and hydrophobic blocks, on which the physico-chemical properties of the polymers depend, can be controlled during manufacture, enabling the production of poloxamers tailored to specific applications. [Pg.765]

Book II investigates the dynamical conditions of fluid motion. Book III displays the law of gi avitatioii at work in the solar system. It is demonstrated from the revolutions of the six known planets, including Earth, and their satellites, though Newton could never quite perfect the difficult theory of the Moon s motion. It is also demonstrated from the motions of comets. The gravitational forces of the heavenly bodies are used to calculate their relative masses. The tidal ebb and flow and the precession of the equinoxes is explained m terms of the forces exerted by the Sun and Moon. These demonstrations are carried out with precise calculations. [Pg.846]

The API (American Petroleum Institute) gravity is another way to express the relative masses of crude oils. The API gravity could he calculated mathematically using the following equation ... [Pg.20]

Particle Location Relative Charge Relative Mass ... [Pg.29]

Individual atoms are far too small to be weighed on a balance. However, as you will soon see, it is possible to determine quite accurately the relative masses of different atoms and molecules. Indeed, it is possible to go a step further and calculate the actual masses of these tiny building blocks of matter. [Pg.51]

Relative masses of atoms of different elements are expressed in terms of their atomic masses (often referred to as atomic weights). The atomic mass of an element indicates how heavy, on the average, one atom of that element is compared with an atom of another element... [Pg.51]

Atomic masses give relative masses of different atoms. [Pg.51]

For most purposes in chemistry, it is sufficient to know the relative masses of different atoms. Sometimes, however, it is necessary to go one step further and calculate the mass in grams of individual atoms. Let us consider how this can be done. [Pg.53]

Even if c (Equation 5-12) is fairly large, an element cannot be precisely determined—or may even escape detection—if it is present in too small amount relative to the matrix. What amount is too small depends not only upon the relative mass (or weight-fraction) of element sought but also upon the mass absorption coefficient of the matrix, as Equations 5-8 and 5-9 imply. [Pg.139]

FIGURE B.6 The mass spectrum of neon. The locations of the peaks tell us the relative masses of the atoms, and the intensities tell us the relative numbers of atoms having each mass. [Pg.42]

The curve marked ion-dipole is based on the classical cross-section corresponding to trajectories which lead to intimate encounters (9, 13). The measured cross-sections differ more dramatically from the predictions of this theory than previously measured cross-sections for exothermic reactions (7). The fast fall-off of the cross-section at high energy is quite close to the theoretical prediction (E 5 5) (2) based on the assumption of a direct, impulsive collision and calculation of the probability that two particles out of three will stick together. The meaning of this is not clear, however, since neither the relative masses of the particles nor the energy is consistent with this theoretical assumption. This behavior is, however, probably understandable in terms of competition of different exit channels on the basis of available phase space (24). [Pg.29]

FIGURE 9.11 Relative mass change as a result of water absorption and loss in a solid piece of recombinant resilin prepared from a 20% protein solution in phosphate-buffered sahne (PBS), cross-linked using peroxidase (see [29] supplementary material). The fuUy swollen sample is designated 100. (Data courtesy of Shekibi, Y., Naim, K., Bastow, T.J., and HiU, A.J., The states of water in a protein based hydrogel. Internal CSIRO... [Pg.265]

In addition to obtaining Information about the size, relative mass, and structure of the platinum crystallites, the STEM can provide a qualitative evaluation of the metal distribution from support particle to support particle. In general, the distribution of platinum was more uniform on alumina than silica, however, optimal uniformity was not achieved. This observation was based on wide variations In Pt/Sl and Pt/Al ratios measured by EDS. [Pg.377]

Bruyant-Vannier et al [5] have shown that pectin methyltransferases solubilized from endomembranes of flax cells consisted of several polypeptides, the molecular relative mass of which varied from very low (Mr < 5,000) to very high (Mr ca 200,000) values. [Pg.712]

Observe the influence of the magnitudes of the relative mass transfer coefficients K] and K2 on the dynamics of the approach to equilibrium. [Pg.533]

The wheat sample residue level is determined from the relative mass spectral responses of the analytes to the corresponding isotopically labeled internal standards. The sample relative response is compared with the average relative response of a standard solution of analyte and internal standard analyzed before and after the sample (bracketing standards). Both samples and standards receive the same amount, 100 ng, of each internal standard to facilitate the comparison. The calculations to determine the residue level in wheat tissues are outlined in Section 7.3.1. [Pg.494]

We may, I think, without too much rashness, assume that there is some substance or substances in the nerve endings or [salivary] gland cells with which both atropine and pilocarpine are capable of forming compounds. On this assumption, then, the atropine or pilocarpine compounds are formed according to some law of which their relative mass and chemical affinity for the substance are factors. [Pg.5]

Table II. Relative mass intensities evolved from the 1 4 chloride complex at three temperatures during thermal decomposition in the mass spectrometer. Nominal temperature values are given. Table II. Relative mass intensities evolved from the 1 4 chloride complex at three temperatures during thermal decomposition in the mass spectrometer. Nominal temperature values are given.
Hence, Ke may be determined experimentally by assaying the concentrations in the donor solution. It is noted that the relative donor concentration in Eqs. (125) and (126) may be replaced by the relative mass in the donor solution. [Pg.317]


See other pages where Relative masses is mentioned: [Pg.269]    [Pg.15]    [Pg.454]    [Pg.517]    [Pg.19]    [Pg.19]    [Pg.130]    [Pg.142]    [Pg.144]    [Pg.277]    [Pg.278]    [Pg.52]    [Pg.118]    [Pg.218]    [Pg.871]    [Pg.119]    [Pg.711]    [Pg.309]    [Pg.311]    [Pg.42]    [Pg.131]    [Pg.137]    [Pg.370]   
See also in sourсe #XX -- [ Pg.2 , Pg.251 , Pg.438 ]

See also in sourсe #XX -- [ Pg.73 ]




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