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Repulsive energy

H = (kinetic energy) + (kinetic energy+ (repulsion) + (repulsion)gg + (attraction... [Pg.11]

In Equation (10), Vc represents a hard-core repulsion that is entropic in nature since it is linearly dependent on temperature in the expression for energy. Repulsion is generally associated with enthalpic interactions and we can consider the effect of an enthalpic interaction. Since Vc is associated with a single Kuhn unit we consider the average enthalpy of interaction per pair-wise interaction and the number of pair-wise interactions per Kuhn unit,... [Pg.129]

Table 5.37 Lattice energy terms for C2/c pyroxenes. Values in kJ/mole. bhf = energy of Born-Haber-Fayans thermochemical cycle U- = lattice energy Ec = coulombic energy = repulsive energy Edd = dipole-dipole interactions E q = dipole quadrupole interactions =... Table 5.37 Lattice energy terms for C2/c pyroxenes. Values in kJ/mole. bhf = energy of Born-Haber-Fayans thermochemical cycle U- = lattice energy Ec = coulombic energy = repulsive energy Edd = dipole-dipole interactions E q = dipole quadrupole interactions =...
Coulomb energy repulsion energy dispersion energy zero point energy... [Pg.43]

In seeking to rationalize the repulsive structure found in the He (2 S) + Ar,Kr,Xe,D2 interactions, we examine the model for noble-gas partners proposed by Siska et al.108,109 1,2 and the rationale presented by Isaacson et al.121 for He (l S) + D2. In the model potential function of Siska et al.108- 109 tjje iow energy repulsion is represented by a switchover from alkalilike—closed-shell repulsive behavior to ion core (He+)-—closed-shell Rydberg-like behavior with decreasing internuclear distance in other words,... [Pg.567]

Physical chemists established a process called self-organization in which water-insoluble amphiphiles firstly form a molecular brush on the water surface and then assemble to spherical droplets or bladders in bulk water if a threshold concentration (cmc, critical micellar concentration) is surpassed. It was also shown that the self-organization of molecular mono- and bilayers is commonly not followed by crystal growth which would normally be favoured as it diminishes surface energies. Repulsive hydration and undulation effects were held responsible for preventing the growth of the delicate bilayer structures to 3D crystals. [Pg.2]

It was also shown that the potential energy repulsion term is related to the change in enthalpy (equation 87). [Pg.54]

Figure 8.18. Simplified scheme of the forms of energy (repulsive and attractive) that combine to give the total energy of M -saturated and M -saturated smectite as a function of the interlayer spacing in water. Figure 8.18. Simplified scheme of the forms of energy (repulsive and attractive) that combine to give the total energy of M -saturated and M -saturated smectite as a function of the interlayer spacing in water.
Figure 6.—Continued. C, Predicted electrical drift contribution to molecular transport across one of the two cubic cell membranes. (Weaver, J. C. Barnett, A. Wang, M. W. B/iss, J. G., unpublished). A hypothetical series of molecules, a// with unit charge (zs = l) was used to test the relative importance of different size pores in the pore population. More realistic predictions would use estimates of the size (radius rs), shape (a form factor), and the Bom energy repulsion (zs>eff — zm, where m is a number in the range 1 < m < 2). Figure 6.—Continued. C, Predicted electrical drift contribution to molecular transport across one of the two cubic cell membranes. (Weaver, J. C. Barnett, A. Wang, M. W. B/iss, J. G., unpublished). A hypothetical series of molecules, a// with unit charge (zs = l) was used to test the relative importance of different size pores in the pore population. More realistic predictions would use estimates of the size (radius rs), shape (a form factor), and the Bom energy repulsion (zs>eff — zm, where m is a number in the range 1 < m < 2).
Here p(z) is the local density of the adsorbed fluid at a distance z from one of the walls of the pore, f(z) is the intrinsic molecular Helmholtz energy of the adsorbate phase, p is the chemical potential. The free energy f(z) comprises tire ideal, mean-field attractive terms, and the excess fine energy (repulsive) term as a function of so-called smoothed weighted average density. [Pg.150]

P. von Brentano, On the mixing of two bound and unbound levels Energy repulsion and width athactions, Phys. Rep. 264 (1996) 57. [Pg.50]

The protecting action itself shows two different elements. When the tails of molecules bonded to two particles approach each other, the increase in local concentration leads to an increase in free energy (repulsion), which is an osmotic effect. At the same time, some tails may not fit in the space between the particles, decreasing the number of conformational possibilities, which promotes a loss of entropy. This is the volume restriction effect. [Pg.667]

VII. TOTAL POTENTIAL ENERGY (REPULSION + ATTRACTION) FOR TWO PLATES, AND APPLICATION TO COLLOID STABILITY. [Pg.106]

In contrast with nuclear fission where a large nucleus is split into two more stable nuclei, fusion relies on the formation of larger stable nuclei from small nuclei. The main difference is that fusion requires an initial high temperature of millions of degrees to overcome the energy repulsion barrier of the nuclei. In the fusion H-bomb, the high temperature (10 K) is achieved by a fission bomb. [Pg.126]


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See also in sourсe #XX -- [ Pg.71 ]

See also in sourсe #XX -- [ Pg.201 ]

See also in sourсe #XX -- [ Pg.13 , Pg.17 , Pg.288 ]




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Apolar-polar repulsive free energy

Bond Energies and Pauli Repulsions in Homonuclear Diatomics

Bonds repulsive energy

Born repulsion energy

Carbenes electron repulsion energy

Coulomb energy electron repulsion

Coulomb repulsion energy, interelectronic

Coulomb repulsion free energy

Coulomb repulsive energy

Coulombic energy of repulsion

Coulombic repulsion energy

Dispersion-repulsion energy

Electrical repulsive potential energy

Electron Coulomb repulsion energy difference

Electron repulsion energy

Electrostatic repulsion energy

Electrostatic repulsive energy

Electrostatic repulsive energy, electrically

Energy Coulomb repulsion

Energy interionic repulsion

Energy of electrostatic repulsion

Energy repulsive interaction

Energy short-range repulsion

Energy steric repulsion

Exchange repulsion energy

Fines repulsive energy between

Gibbs energy of repulsion

Gibbs energy repulsion

Headgroup repulsion free energy

Inner repulsion energy

Interaction energy electrostatic repulsion

Interaction energy exchange repulsion

Interaction energy steric repulsion

Interelectron repulsion energy

Interelectronic repulsion energy

Interelectronic repulsion energy complexes

Internuclear repulsion energy

Lattice repulsion energy

Ligand repulsion energy

Ligand repulsive energy

Nuclear repulsion energy

Orbital energy electron repulsion and

Outer repulsion energy

Oxygen repulsion energy coefficients

Pauli (exchange) repulsion energy

Polarizable continuum model repulsion energies

Potential energy attraction-interaction-repulsion

Potential energy of repulsion

Potential energy surface repulsive

Racah interelectronic repulsion energy

Representation Repulsion energy

Repulsion energy

Repulsion energy

Repulsion energy coefficients

Repulsion energy conversion mechanism

Repulsion energy, charge-transfer

Repulsion energy, charge-transfer transitions

Repulsive energy between protons

Repulsive energy release

Repulsive energy, between electrons

Repulsive energy, electrically charged

Repulsive exchange energy

Repulsive potential energy

Self-repulsion energy

Self-repulsion energy, wave function calculations

Semiempirical molecular orbital method repulsive energy

Short-range repulsive energies

Square antiprisms repulsion energy coefficients

Squares repulsion energy coefficients

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