Hard spheres

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Template:Short description In statistical mechanics, hard spheres are widely used as model particles in fluids and solids. They are defined simply as impenetrable spheres that cannot overlap in space. They mimic the extremely strong ("infinitely elastic bouncing") repulsion that atoms and spherical molecules experience at very close distances. Hard spheres systems are studied by analytical means, by molecular dynamics simulations, and by the experimental study of certain colloidal model systems.

Beside being a model of theoretical significance, the hard-sphere system is used as a basis in the formulation of several modern, predictive equations of state for real fluids through the statistical associating fluid theory (SAFT) approach, and models for transport properties in gases through Chapman–Enskog theory.

Formal definition

Hard spheres of diameter σ are particles with the following pairwise interaction potential:

V(𝐫1,𝐫2)={0if|𝐫1𝐫2|σif|𝐫1𝐫2|<σ

where 𝐫1 and 𝐫2 are the positions of the two particles.

Hard-spheres gas

The first three virial coefficients for hard spheres can be determined analytically

B2v0=4B3v02=10B4v03=71235+219235π+413135πarccos1318.365

Higher-order ones can be determined numerically using Monte Carlo integration. We list

B5v04=28.24±0.08B6v05=39.5±0.4B7v06=56.5±1.6

A table of virial coefficients for up to eight dimensions can be found on the page Hard sphere: virial coefficients.[1]

File:Hard-sphere phase diagram pressure packing fraction.svg
Phase diagram of hard sphere system (Solid line - stable branch, dashed line - metastable branch): Pressure P as a function of the volume fraction (or packing fraction) η

The hard sphere system exhibits a fluid-solid phase transition between the volume fractions of freezing ηf0.494 and melting ηm0.545. The pressure diverges at random close packing ηrcp0.644 for the metastable liquid branch and at close packing ηcp=2π/60.74048 for the stable solid branch.

Hard-spheres liquid

The static structure factor of the hard-spheres liquid can be calculated using the Percus–Yevick approximation.

Carnahan–Starling equation of state

A simple, yet popular equation of state describing systems of pure hard spheres was developed in 1969 by Norman F. Carnahan and K. E. Starling.[2] By expressing the compressibility of a hard-sphere system as a geometric series, the expression

Z=pVnRT=1+η+η2η3(1η)3

is obtained, where η is the packing fraction, given by

η=NAπnσ36V

where NA is Avogadro's number, n/V is the molar density of the fluid, and σ is the diameter of the hard-spheres. From this Equation of State, one can obtain the residual Helmholtz energy,[3]

AresnRT=4η3η2(1η)2,

which yields the residual chemical potential

μresRT=8η9η2+3η3(1η)3.

One can also obtain the value of the radial distribution function, g(r), evaluated at the surface of a sphere,[3]

g(σ)=112η(1η)3.

The latter is of significant importance to accurate descriptions of more advanced intermolecular potentials based on perturbation theory, such as SAFT, where a system of hard spheres is taken as a reference system, and the complete pair-potential is described by perturbations to the underlying hard-sphere system. Computation of the transport properties of hard-sphere gases at moderate densities using revised Enskog theory also relies on an accurate value for g(σ), and the Carnahan–Starling equation of state has been used for this purpose to large success.[4]

See also

Literature

  • J. P. Hansen and I. R. McDonald Theory of Simple Liquids Academic Press, London (1986)
  • Hard sphere model page on SklogWiki.

References

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