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In 1923, Peter Debye and Erich Hückel reported the first successful theory for the distribution of charges in ionic solutions. [7] The framework of linearized Debye–Hückel theory subsequently was applied to colloidal dispersions by S. Levine and G. P. Dube [8] [9] who found that charged colloidal particles should experience a strong medium-range repulsion and a weaker long-range attraction.
The induced dipole forces appear from the induction (also termed polarization), which is the attractive interaction between a permanent multipole on one molecule with an induced (by the former di/multi-pole) 31 on another. [12] [13] [14] This interaction is called the Debye force, named after Peter J. W. Debye.
The Born–Landé equation is a means of calculating the lattice energy of a crystalline ionic compound. In 1918 [ 1 ] Max Born and Alfred Landé proposed that the lattice energy could be derived from the electrostatic potential of the ionic lattice and a repulsive potential energy term.
The three-term virial equation or a cubic virial equation of state = + + has the simplicity of the Van der Waals equation of state without its singularity at v = b. Theoretically, the second virial coefficient represents bimolecular attraction forces, and the third virial term represents the repulsive forces among three molecules in close contact.
Double layer forces occur between charged objects across liquids, typically water. This force acts over distances that are comparable to the Debye length, which is on the order of one to a few tenths of nanometers. The strength of these forces increases with the magnitude of the surface charge density (or the electrical surface potential). For ...
The surface energy of a liquid may be measured by stretching a liquid membrane (which increases the surface area and hence the surface energy). In that case, in order to increase the surface area of a mass of liquid by an amount, δA, a quantity of work, γ δA, is needed (where γ is the surface energy density of the liquid).
The positive part models the repulsive forces as the electron clouds of the two molecules overlap. The radius for zero interaction potential is therefore appropriate for estimating (or defining) the collision cross section in kinetic gas theory, and the r-parameter (conf. r , r i {\displaystyle r,r_{i}} ) is therefore called kinetic radius .
This is the virial equation of state and describes a real gas. Since higher order virial coefficients are generally much smaller than the second coefficient, the gas tends to behave as an ideal gas over a wider range of pressures when the temperature reaches the Boyle temperature (or when c = 1 V m {\textstyle c={\frac {1}{V_{m}}}} or P ...