1-dimensional hard rods
1-dimensional hard rods (sometimes known as a Tonks gas [1]) consist of non-overlapping line segments of length who all occupy the same line which has length . One could also think of this model as being a string of hard spheres confined to 1 dimension (not to be confused with 3-dimensional hard rods). The model is given by the intermolecular pair potential:
where is the position of the center of the k-th rod, along with an external potential. Thus, the Boltzmann factor is
The whole length of the rod must be inside the range:
Canonical Ensemble: Configuration Integral[edit]
The statistical mechanics of this system can be solved exactly. Consider a system of length defined in the range . The aim is to compute the partition function of a system of hard rods of length . Consider that the particles are ordered according to their label: ; taking into account the pair potential we can write the canonical partition function of a system of particles as:
Variable change: ; we get:
Therefore:
Thermodynamics[edit]
In the thermodynamic limit (i.e. with , remaining finite):
Equation of state[edit]
Using the thermodynamic relations, the pressure (linear tension in this case) can be written as:
The compressibility factor is
where ; is the fraction of volume (i.e. length) occupied by the rods. 'id' labels the ideal and 'ex' the excess part.
It was shown by van Hove [2] that there is no fluid-solid phase transition for this system (hence the designation Tonks gas).
Chemical potential[edit]
The chemical potential is given by
with ideal and excess part separated:
Isobaric ensemble: an alternative derivation[edit]
Adapted from Reference [3]. If the rods are ordered according to their label: the canonical partition function can also be written as:
where does not appear one would have analogous expressions by permuting the label of the (distinguishable) rods. is the Boltzmann factor of the hard rods, which is if and otherwise.
A variable change to the distances between rods: Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle y_k = x_k - x_{k-1} } results in
- Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle Z = \int_0^{\infty} d y_0 \int_0^{\infty} d y_1 \cdots \int_0^{\infty} d y_{N-1} f(y_0) f(y_1) \cdots f(y_{N-1}) \delta \left( \sum_{i=0}^{N-1} y_i-L \right): }
the distances can take any value as long as they are not below Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle \sigma} (as enforced by Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle f(y)} ) and as long as they add up to Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle L} (as enforced by the Dirac delta). Writing the later as the inverse Laplace transform of an exponential:
Exchanging integrals and expanding the exponential the Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle N} integrals decouple:
- Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle Z = \frac{1}{2\pi i } \int_{-\infty}^{\infty} ds e^{ L s } \left\{ \int_0^{\infty} d y f(y) e^{ - s y } \right\}^N. }
We may proceed to invert the Laplace transform (e.g. by means of the residues theorem), but this is not needed: we see our configuration integral is the inverse Laplace transform of another one,
- Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle Z'(s)= \left\{ \int_0^{\infty} d y f(y) e^{ - s y } \right\}^N, }
so that
- Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle Z'(s) = \int_0^{\infty} ds e^{ L s } Z(L). }
This is precisely the transformation from the configuration integral in the canonical () ensemble to the isobaric (Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle N,T,p} ) one, if one identifies Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle s=p/k T} . Therefore, the Gibbs energy function is simply Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle G=-kT\log Z'(p/kT) } , which easily evaluated to be Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle G=kT N \log(p/kT)+p\sigma N} . The chemical potential is , and by means of thermodynamic identities such as Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle \rho=\partial p/\partial \mu} one arrives at the same equation of state as the one given above.
Confined hard rods[edit]
References[edit]
- ↑ Lewi Tonks "The Complete Equation of State of One, Two and Three-Dimensional Gases of Hard Elastic Spheres", Physical Review 50 pp. 955- (1936)
- ↑ L. van Hove, "Sur L'intégrale de Configuration Pour Les Systèmes De Particules À Une Dimension", Physica, 16 pp. 137-143 (1950)
- ↑ J. M. Ziman Models of Disorder: The Theoretical Physics of Homogeneously Disordered Systems, Cambridge University Press (1979) ISBN 0521292808
- ↑ A. Robledo and J. S. Rowlinson "The distribution of hard rods on a line of finite length", Molecular Physics 58 pp. 711-721 (1986)
Related reading
- L. van Hove "Quelques Propriétés Générales De L'intégrale De Configuration D'un Système De Particules Avec Interaction", Physica, 15 pp. 951-961 (1949)
- Zevi W. Salsburg, Robert W. Zwanzig, and John G. Kirkwood "Molecular Distribution Functions in a One-Dimensional Fluid", Journal of Chemical Physics 21 pp. 1098-1107 (1953)
- Robert L. Sells, C. W. Harris, and Eugene Guth "The Pair Distribution Function for a One-Dimensional Gas", Journal of Chemical Physics 21 pp. 1422-1423 (1953)
- Donald Koppel "Partition Function for a Generalized Tonks' Gas", Physics of Fluids 6 609 (1963)
- J. L. Lebowitz, J. K. Percus and J. Sykes "Time Evolution of the Total Distribution Function of a One-Dimensional System of Hard Rods", Physical Review 171 pp. 224-235 (1968)
- Gerardo Soto-Campos, David S. Corti, and Howard Reiss "A small system grand ensemble method for the study of hard-particle systems", Journal of Chemical Physics 108 pp. 2563-2570 (1998)
- Paolo V. Giaquinta "Entropy and Ordering of Hard Rods in One Dimension", Entropy 10 pp. 248-260 (2008)