Big Chemical Encyclopedia

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

Articles Figures Tables About

Lorentz mean

Partial molar volumes can be expressed by means of the Beattie-Bridgman equation similarly to the case in which virial expansion was used, functional relationships being defined with the use of relation (6.47). Either one of the three approximations defined by relations (6.87) — (6.89) is used for all constants or, as recommended by Beattie et al., the geometrical mean is taken for the constants Aom and c , the Lorentz mean for Bq and the arithmetic mean for a , b , so that... [Pg.184]

Proceeding similarly to the preceding case and introducing, as recommended by the authors of, the arithmetic mean for the interaction terms in constant Bq, the geometric mean for Aq, Cq, y and the Lorentz mean for a, b, c, a, we obtain the following expressions for the constants of the mixture... [Pg.186]

The scattered intensity measured from the isotropic three-dimensional object can be transfonned to the onedimensional mtensity fiinction/j(<3 ) by means of the Lorentz correction [15]... [Pg.1406]

The collision terms may be simplified by using the condition that mjM is very small this leads to the Lorentz approximation. If there were no electric field, the equilibrium situation would be one in which the mean kinetic energy of the electrons would be equal to that of the... [Pg.47]

Figure 9.9. Infinite functions in a periodic world. Using a function (black line) as an orientation function means to wrap it around the orientation sphere. Only one branch of a LORENTZ distribution at the right side of the equator is sketched. Shape change occurs... [Pg.221]

If X is space-like and the events are designated such that t2 > 11, then c(ti — f2) < z — z2, and it is therefore possible to find a velocity v < c such that ic(t[ — t 2) = X vanishes. Physically the vanishing of X means that if the distance between two events is space-like, then one can always find a Lorentz system in which the two events have the same time coordinate in the selected frame. On the other hand, for time-like separations between events one cannot find a Lorentz transformation that will make them simultaneous, or change the order of the time sequence of the two events. The concepts "future" and "past" are invariant and causality is preserved. That the sequence of events with space-like separations can be reversed does not violate causality. As an example it is noted that no influence eminating from earth can affect an object one light-year away within the next year. [Pg.147]

It is to be expected that the equations relating electromagnetic fields and potentials to the charge current, should bear some resemblance to the Lorentz transformation. Stating that the equations for A and (j> are Lorentz invariant, means that they should have the same form for any observer, irrespective of relative velocity, as long as it s constant. This will be the case if the quantity (Ax, Ay, Az, i/c) = V is a Minkowski four-vector. Easiest would be to show that the dot product of V with another four-vector, e.g. the four-gradient, is Lorentz invariant, i.e. to show that... [Pg.151]

The generation of invariants in the Lorentz transformation of four-vectors has been interpreted to mean that the transformation is equivalent to a rotation. The most general rotation of a four-vector, defined as the quaternion q = w + ix + jy + kz is given by [39]... [Pg.157]

The KG equation is Lorentz invariant, as required, but presents some other problems. Unlike Schrodinger s equation the KG equation is a second order differential equation with respect to time. This means that its solutions are specified only after an initial condition on bothand d /dt has been given. However, in contrast to k, d /dt has no direct physical interpretation [61]. Should the KG equation be used to define an equation of continuity, as was done with Schrodinger s equation (4), it is found to be satisfied by... [Pg.221]

This equation can be interpreted as the drift term of a collisionless Boltzmann equation for the one-particle Wigner distribution p(q,p). To see that, let us explore the physical meaning of p(q,p) in this context. First note that p(q, p ) is in principle a Lorentz scalar. Thus an invariant solution of Eq. (59) is... [Pg.209]

Mean molecular polarizability can be calculated through the Lorenz-Lorentz- Equation from refractive index, n, molecular weight, MW, and density, d, of a compound, demonstrating that the parameters can be derived from these elementary molecular properties (Figure 3). [Pg.263]

Figure 4.12 Magnification of the region near Lq in Figure 4.11. L is the Lorentz point (the Lane point corrected for the mean refractive index). A is one of the tie-points selected on the dispersion surface, and o and are the deviation parameters at that point (shown on branch 2)... Figure 4.12 Magnification of the region near Lq in Figure 4.11. L is the Lorentz point (the Lane point corrected for the mean refractive index). A is one of the tie-points selected on the dispersion surface, and o and are the deviation parameters at that point (shown on branch 2)...
Consideration of the symmetry of the Poincare group also shows that the cyclic theorem is independent of Lorentz boosts in any direction, and also reveals the physical meaning of the E(2) little group of Wigner. This group is unphysical for a photon without mass, but is physical for a photon with mass. This proves that Poincare symmetry leads to a photon with identically nonzero mass. The proof is as follows. Consider in the particle interpretation the PL vector... [Pg.236]

Owing to the Lorentz factor in formula (4.54), when v approaches c, we have b etf—meaning that a molecule can be excited by a very distant passing particle, which is in contradiction with reality. This is a consequence of the fact that in our derivation (as in Ref. 150) we made no allowance for the weakening of the interaction between a charged particle and molecule when b> a, which is due to the polarization of the medium. The account of dielectric properties of the medium should lead to finite values of b eff even at v = c. [Pg.303]

When a non-centrosymmetric solvent is used, there is still hyper-Rayleigh scattering at zero solute concentration. The intercept is then determined by the number density of the pure solvent and the hyperpolarizability of the solvent. This provides a means of internal calibration, without the need for local field correction factors at optical frequencies. No dc field correction factors are necessary, since in HRS, unlike in EFISHG, no dc field is applied. By comparing intercept and slope, a hyperpolarizability value can be deduced for the solute from the one for the solvent. This is referred to as the internal reference method. Alternatively, or when the solvent is centrosymmetric, slopes can be compared directly. One slope is then for a reference molecule with an accurately known hyperpolarizability the other slope is for the unknown, with the hyperpolarizability to be determined. This is referred to as the external reference method. If the same solvent is used, then no field correction factor is necessary. When another solvent needs to be used, the different refractive index calls for a local field correction factor at optical frequencies. The usual Lorentz correction factors can be used. [Pg.383]

The Lorentz-Lorenz equation can be used to express the components of the refractive index tensor in terms of the polarizability tensor. Recognizing that the birefringence normalized by the mean refractive index is normally very small, ( A/i / 1), it is assumed that Aa /a 1, where the mean polarizability is a = (al + 2oc2)/3 and the polarizability anisotropy is Aa = a1-a2. It is expected that the macroscopic refractive... [Pg.112]


See other pages where Lorentz mean is mentioned: [Pg.182]    [Pg.182]    [Pg.228]    [Pg.494]    [Pg.132]    [Pg.46]    [Pg.573]    [Pg.74]    [Pg.52]    [Pg.763]    [Pg.145]    [Pg.314]    [Pg.60]    [Pg.102]    [Pg.87]    [Pg.101]    [Pg.160]    [Pg.218]    [Pg.237]    [Pg.684]    [Pg.705]    [Pg.716]    [Pg.700]    [Pg.258]    [Pg.1209]    [Pg.119]    [Pg.456]    [Pg.560]    [Pg.583]    [Pg.693]    [Pg.302]    [Pg.161]    [Pg.165]    [Pg.615]   
See also in sourсe #XX -- [ Pg.184 ]




SEARCH



Lorentz

© 2024 chempedia.info