Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Inelastic parameter

Xps is a surface sensitive technique as opposed to a bulk technique because electrons caimot travel very far in soHds without undergoing energy loss. Thus, even though the incident x-rays penetrate the sample up to relatively large depths, the depth from which the electron information is obtained is limited by the "escape depth" of the photoemitted electrons. This surface sensitivity of xps is quantitatively defined by the inelastic mean free path parameter which is given the symbol X. This parameter is defined to be the distance an electron travels before engaging in an interaction in which it experiences an energy loss. [Pg.276]

The normality conditions (5.56) and (5.57) have essentially the same forms as those derived by Casey and Naghdi [1], [2], [3], but the interpretation is very different. In the present theory, it is clear that the inelastic strain rate e is always normal to the elastic limit surface in stress space. When applied to plasticity, e is the plastic strain rate, which may now be denoted e", and this is always normal to the elastic limit surface, which may now be called the yield surface. Naghdi et al. by contrast, took the internal state variables k to be comprised of the plastic strain e and a scalar hardening parameter k. In their theory, consequently, the plastic strain rate e , being contained in k in (5.57), is not itself normal to the yield surface. This confusion produces quite different results. [Pg.139]

Values of the total cross-section a a for A1 Ka, radiation, relative to the carbon Is level, have been calculated by Scofield [2.7], and of the asymmetry parameter /Ja by Redman et al. [2.8]. Seah and Dench [2.3] have compiled many measurements of the inelastic mean free path, and for elements the best-fit relationship they found was ... [Pg.17]

The utility of K or any elastic plastic fracture mechanics (EPFM) parameter to describe the mechanical driving force for crack growth is based on the ability of that parameter to characterize the stress-strain conditions at the crack tip in a maimer which accounts for a variety of crack lengths, component geometries and loading conditions. Equal values of K should correspond to equal crack tip stress-strain conditions and, consequently, to equivalent crack growth behavior. In such a case we have mechanical similitude. Mechanical similitude implies equivalent crack tip inelastic zones and equivalent elastic stress fields. Fracture mechanics is... [Pg.495]

Here 0(a) is the density of distribution over a after collision and tc is the average collision time. The popular Keilson-Storer model, presented in Eq. (1.6) and Fig. 1.2, uses the single numerical parameter y to characterize the strength of inelastic collisions. It will be discussed in Section 1.3. [Pg.15]

In either case, the information on the vibrational transition is contained in the energy difference between the excitation radiation and the inelastically scattered Raman photons. Consequently, the parameters of interest are the intensities of the lines and their position relative to the Rayleigh line, usually expressed in wavenumbers (cm 1). As the actually recorded emissions all are in the spectral range determined by the excitation radiation, Raman spectroscopy facilitates the acquisition of vibrational spectra through standard VIS and/or NIR spectroscopy. [Pg.126]

Knockenmuss R, Hipps KW (1982) Some proposed modifications in the theory of inelastic electron tunneling spectroscopy and the source of parameters utilized. J Phys Chem 86 4477-4480... [Pg.211]

Fig. 20. Excess compressibility yIS for a system of inelastic hard spheres, as function of the coefficient of normal restitution, for one solid fraction (as = 0.05). The excess compressibility has been normalized by the excess compressibility y is of the elastic hard spheres system. Other simulation parameters are as in Fig. 19. Fig. 20. Excess compressibility yIS for a system of inelastic hard spheres, as function of the coefficient of normal restitution, for one solid fraction (as = 0.05). The excess compressibility has been normalized by the excess compressibility y is of the elastic hard spheres system. Other simulation parameters are as in Fig. 19.
Thermal distributions of NO(u 2, J, A Ej,) states were observed, wherein the population in any level was determined by the internal energy and the parameter Tr. and independent of spin-orbit state or lambda doublet species. This is in contrast to the rotational rainbows, the propensities for preferential population in the Il(A ) lambda doublet species and the Fj spin orbit state which were observed in direct inelastic scattering of NO/Ag(l 11). [Pg.56]

Table I. Values of parameters characterising pre-gel intramolecular reaction (v,b,(f-2)/(vb ) ) (5-7,12) and the extents of post-gel intramolecular reaction which, in the limit of ideal gelling systems, lead to inelastic loop formation at complete reaction (p g). The values of pj g define the indicated values of Mg/M° and the reductions in shear moduli of the dry networks relative to those of the perfect networks (G/G° = Mc/Mc). The values of Pr g in the limit of reactants of infinite molar mass (v = < ) are denoted p°>°° in the text... Table I. Values of parameters characterising pre-gel intramolecular reaction (v,b,(f-2)/(vb ) ) (5-7,12) and the extents of post-gel intramolecular reaction which, in the limit of ideal gelling systems, lead to inelastic loop formation at complete reaction (p g). The values of pj g define the indicated values of Mg/M° and the reductions in shear moduli of the dry networks relative to those of the perfect networks (G/G° = Mc/Mc). The values of Pr g in the limit of reactants of infinite molar mass (v = < ) are denoted p°>°° in the text...
Figure 7. Dependence of post-gel intramolecular reaction leading to inelastic loops in the limit of ideal gelling systems (p° g) on the parameters affecting pre-gel intramolecular reaction ((f-2)/(vb ) ). Figure 7. Dependence of post-gel intramolecular reaction leading to inelastic loops in the limit of ideal gelling systems (p° g) on the parameters affecting pre-gel intramolecular reaction ((f-2)/(vb ) ).
Extrapolation of pj. g to the limit of zero pre-gel intramolecular reaction for given reaction systems shows that post-gel intramolecular reaction always results in network defects, with significant increases in Mg above Mg. Such post-gel intramolecular reaction is characterised as pg g. The variation of pg g with intramolecular-reaction parameters shows that even in the limit of infinite molar mass, i.e. no spatial correlation between reacting groups, inelastic loops will be formed. The formation may be considered as a law-of-mass-action effect, essentially the random reaction of functional groups. Intramolecular reaction under such conditions (p2 ) must be post-gel and may be treated using classical polymerisation theory. [Pg.46]


See other pages where Inelastic parameter is mentioned: [Pg.638]    [Pg.1308]    [Pg.2553]    [Pg.2911]    [Pg.281]    [Pg.1882]    [Pg.17]    [Pg.497]    [Pg.502]    [Pg.178]    [Pg.101]    [Pg.161]    [Pg.195]    [Pg.439]    [Pg.575]    [Pg.575]    [Pg.491]    [Pg.171]    [Pg.159]    [Pg.200]    [Pg.365]    [Pg.56]    [Pg.69]    [Pg.15]    [Pg.54]    [Pg.139]    [Pg.518]    [Pg.523]    [Pg.108]    [Pg.82]    [Pg.87]    [Pg.221]    [Pg.499]    [Pg.97]    [Pg.45]    [Pg.13]   


SEARCH



Inelastic

Inelasticity

© 2024 chempedia.info