Density scalar

This is a real, symmetric tensor, the trace of which is the non-negative kinetic energy density (scalar)... 

T. E. Bearden, Formation and Use of Time-Reversal Zones, EM Wave Transduction, Time-Density (Scalar) EM Excitation and Decay, and Spacetime Curvature Engines to Alter Matter and Convert Time Into Energy, Invention Disclosure Document 446522 (Oct. 26, 1998). 

Besides molecular orbitals, other molecular properties, such as electrostatic potentials or spin density, can be represented by isovalue surfaces. Normally, these scalar properties are mapped onto different surfaces see above). This type of high-dimensional visualization permits fast and easy identification of the relevant molecular regions. 

In the CHS model only nearest neighbors interact, and the interactions between amphiphiles in the simplest version of the model are neglected. In the case of the oil-water symmetry only two parameters characterize the interactions b is the strength of the water-water (oil-oil) interaction, and c describes the interaction between water (oil) and an amphiphile. The interaction between amphiphiles and ordinary molecules is proportional to a scalar product between the orientation of the amphiphile and the distance between the particles. In Ref. 15 the CHS model is generalized, and M orientations of amphiphiles uniformly distributed over the sphere are considered, with M oo. Every lattice site is occupied either by an oil, water, or surfactant particle in an orientation ujf, there are thus 2 + M microscopic states at every lattice site. The microscopic density of the state i is p.(r) = 1(0) if the site r is (is not) occupied by the state i. We denote the sum and the difference of microscopic oil and water densities by and 2 respectively and the density of surfactant at a point r and an orientation by p (r) = p r,U(). The microscopic densities assume the values = 1,0, = 1,0 and 2 = ill 0- In close-packing case the total density of surfactant ps(r) is related to by p = Ylf Pi = 1 - i i. The Hamiltonian of this model has the following form [15]... 

Just to remind you, the electron density and therefore the exchange potential are both scalar fields they vary depending on the position in space r. We often refer to models that make use of such exchange potentials as local density models. The disagreement between Slater s and Dirac s numerical coefficients was quickly resolved, and authors began to write the exchange potential as... 

The form of the scalar product in terms of Schrddinger amplitudes indicates that if we want to introduce into the theory a probability density it is x(x,f)la which must play this role. In fact, the reason for introducing the Schrddinger amplitude stems precisely from the circumstances that in terms of the latter the scalar product takes the ample form (9-95), and as a consequence of this jY (x.QPd3 may directly be interpreted as the probability of finding the particle within the volume V at (hue K... 

Similar considerations lead to the transformation properties of the one-photon states and of the photon in -operators which create photons of definite momentum and helicity. We shall, however, omit them here. Suffice it to remark that the above transformation properties imply that the interaction hamiltonian density Jf mAz) = transforms like a scalar under restricted inhomogeneous Lorentz transformation... 

The interaction hamiltonian density jin A x) transforms like a scalar ... 

Here it is taken into account that density matrix p, being a scalar, commutates with any rotation operator, and diq defined in Eq. (7.51) is used. After an analogous transformation, in master equation (7.51) there remains the Hamiltonian, which does not depend on e ... 

Assuming that substituted Sb at the surface may work as catalytic active site as well as W, First-principles density functional theory (DFT) calculations were performed with Becke-Perdew [7, 9] functional to evaluate the binding energy between p-xylene and catalyst. Scalar relativistic effects were treated with the energy-consistent pseudo-potentials for W and Sb. However, the binding strength with p-xylene is much weaker for Sb (0.6 eV) than for W (2.4 eV), as shown in Fig. 4. 

Similar convection-diffusion equations to the Navier-Stokes equation can be formulated for enthalpy or species concentration. In all of these formulations there is always a superposition of diffusive and convective transport of a field quantity, supplemented by source terms describing creation or destruction of the transported quantity. There are two fundamental assumptions on which the Navier-Stokes and other convection-diffusion equations are based. The first and most fundamental is the continuum hypothesis it is assumed that the fluid can be described by a scalar or vector field, such as density or velocity. In fact, the field quantities have to be regarded as local averages over a large number of particles contained in a volume element embracing the point of interest. The second hypothesis relates to the local statistical distribution of the particles in phase space the standard convection-diffusion equations rely on the assumption of local thermal equilibrium. For gas flow, this means that a Maxwell-Boltzmann distribution is assumed for the velocity of the particles in the frame-of-reference co-moving with the fluid. Especially the second assumption may break dovm when gas flow at high temperature or low pressure in micro channels is considered, as will be discussed below. 

The electron density of a molecule in the presence of electric perturbation is a scalar field with perturbation expansion [6], [11]... 

Here is the volume density and the scalar component of the attraction field, that is, the force per unit mass. To describe the effect of surface forces, consider front- and the backsides of the volume, dS(x + dxl2,y,z) and dS x—dxl2,y,z), which are perpendicular to the v-axis. Due to the action of the neighboring part of the medium the surface force acting on backside is... 

From the physical point of view it is obvious that there is a relationship between the distribution of density of a fluid and the geometric properties of the scalar field [/.To illustrate this we will proceed from the equation of motion... 

Haberlen, O.D. and Rdsch, N. (1992) A scalar-relativistic extension of the linear combination of Gaussian-type orbitals local density functional method application to AuFl, AuCl and Au2. Chemical Physics Letters, 199, 491-496. 

Suzumura, T., Nakajima, T. and Hirao, K. (1999) Ground-state properties of MH, MCI, and M2 (M—Cu, Ag, and Au) calculated by a scalar relativistic density functional theory International Journal of Quantum Chemistry, 75, lVJ-1. ... 

Schreckenbach, G., Ziegler, T., 1997a, Calculation of NMR Shielding Tensors Based on Density Functional Theory and a Scalar Relativistic Pauli-Type Hamiltonian. Application to Transition Metal Complexes , Int. J. 

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