Difference between revisions of "1-dimensional hard rods"

From SklogWiki
Jump to: navigation, search
m (Added a detail to the introduction)
m (Added some related publications.)
Line 1: Line 1:
'''1-dimensional hard rods''' consist of non-overlapping line segments of length <math>\sigma</math> who all occupy the same line which has  length <math>L</math>. One could also think of this model as being a string of  [[hard sphere model | hard spheres]] confined to 1 dimension (not to be confused with [[3-dimensional hard rods]]). The model is given by the [[intermolecular pair potential]]:
+
'''1-dimensional hard rods''' (sometimes known as a ''Tonks Gas'' <ref>[http://dx.doi.org/10.1103/PhysRev.50.955 Lewi Tonks "The Complete Equation of State of One, Two and Three-Dimensional Gases of Hard Elastic Spheres", Physical Review '''50''' pp. 955- (1936)]</ref>) consist of non-overlapping line segments of length <math>\sigma</math> who all occupy the same line which has  length <math>L</math>. One could also think of this model as being a string of  [[hard sphere model | hard spheres]] confined to 1 dimension (not to be confused with [[3-dimensional hard rods]]). The model is given by the [[intermolecular pair potential]]:
  
 
: <math> \Phi_{12} (x_i,x_j) = \left\{ \begin{array}{lll} 0 & ; & |x_i-x_j| > \sigma \\
 
: <math> \Phi_{12} (x_i,x_j) = \left\{ \begin{array}{lll} 0 & ; & |x_i-x_j| > \sigma \\
Line 9: Line 9:
 
\infty &; & {\mathrm {elsewhere}}. \end{array} \right. </math>
 
\infty &; & {\mathrm {elsewhere}}. \end{array} \right. </math>
 
== Canonical Ensemble: Configuration Integral ==
 
== Canonical Ensemble: Configuration Integral ==
The [[statistical mechanics]] of this system can be solved exactly (see Ref. 1).
+
The [[statistical mechanics]] of this system can be solved exactly.
 
Consider a system of length <math> \left. L \right. </math> defined in the range <math> \left[ 0, L \right] </math>. The aim is to compute the [[partition function]] of a system of <math> \left. N \right. </math> hard rods of length <math> \left. \sigma \right. </math>.
 
Consider a system of length <math> \left. L \right. </math> defined in the range <math> \left[ 0, L \right] </math>. The aim is to compute the [[partition function]] of a system of <math> \left. N \right. </math> hard rods of length <math> \left. \sigma \right. </math>.
 
Consider that the particles are ordered according to their label: <math> x_0 < x_1 < x_2 < \cdots < x_{N-1} </math>;  
 
Consider that the particles are ordered according to their label: <math> x_0 < x_1 < x_2 < \cdots < x_{N-1} </math>;  
Line 51: Line 51:
  
 
== Equation of state ==
 
== Equation of state ==
 
 
Using the [[thermodynamic relations]], the [[pressure]]  (''linear tension'' in this case) <math> \left. p \right. </math> can
 
Using the [[thermodynamic relations]], the [[pressure]]  (''linear tension'' in this case) <math> \left. p \right. </math> can
 
be written as:
 
be written as:
Line 66: Line 65:
  
 
== Isobaric ensemble: an alternative derivation ==
 
== Isobaric ensemble: an alternative derivation ==
Adapted from Reference [4]. If the rods are ordered according to their label: <math> x_0 < x_1 < x_2 < \cdots < x_{N-1} </math> the canonical [[partition function]] can also be written as:
+
Adapted from Reference <ref>J. M. Ziman ''Models of Disorder: The Theoretical Physics of Homogeneously Disordered Systems'', Cambridge University Press (1979) ISBN 0521292808</ref>. If the rods are ordered according to their label: <math> x_0 < x_1 < x_2 < \cdots < x_{N-1} </math> the canonical [[partition function]] can also be written as:
 
: <math>
 
: <math>
 
Z=
 
Z=
Line 127: Line 126:
 
<math>s=p/k T</math>. Therefore, the [[Gibbs energy function]] is simply <math>G=-kT\log Z'(p/kT) </math>, which easily evaluated to be <math>G=kT N \log(p/kT)+p\sigma N</math>. The [[chemical potential]] is <math>\mu=G/N</math>, and by means of thermodynamic identities such as <math>\rho=\partial p/\partial \mu</math> one arrives at the same equation of state as the one given above.
 
<math>s=p/k T</math>. Therefore, the [[Gibbs energy function]] is simply <math>G=-kT\log Z'(p/kT) </math>, which easily evaluated to be <math>G=kT N \log(p/kT)+p\sigma N</math>. The [[chemical potential]] is <math>\mu=G/N</math>, and by means of thermodynamic identities such as <math>\rho=\partial p/\partial \mu</math> one arrives at the same equation of state as the one given above.
 
==Confined hard rods==
 
==Confined hard rods==
#[http://dx.doi.org/10.1080/00268978600101521 A. Robledo and J. S. Rowlinson "The distribution of hard rods on a line of finite length", Molecular Physics '''58''' pp. 711-721 (1986)]
+
<ref>[http://dx.doi.org/10.1080/00268978600101521 A. Robledo and J. S. Rowlinson "The distribution of hard rods on a line of finite length", Molecular Physics '''58''' pp. 711-721 (1986)]</ref>
 
==References==
 
==References==
#[http://dx.doi.org/10.1103/PhysRev.50.955 Lewi Tonks "The Complete Equation of State of One, Two and Three-Dimensional Gases of Hard Elastic Spheres", Physical Review '''50''' pp. 955- (1936)]
+
<references/>
#[http://dx.doi.org/10.1016/0031-8914(49)90059-2  L. van Hove "Quelques Propriétés Générales De L'intégrale De Configuration D'un Système De Particules Avec Interaction", Physica, '''15''' pp. 951-961 (1949)]
+
'''Related reading'''
#[http://dx.doi.org/10.1016/0031-8914(50)90072-3  L. van Hove, "Sur L'intégrale de Configuration Pour Les Systèmes De Particules À Une Dimension", Physica, '''16''' pp. 137-143 (1950)]
+
*[http://dx.doi.org/10.1016/0031-8914(49)90059-2  L. van Hove "Quelques Propriétés Générales De L'intégrale De Configuration D'un Système De Particules Avec Interaction", Physica, '''15''' pp. 951-961 (1949)]
#J. M. Ziman ''Models of Disorder: The Theoretical Physics of Homogeneously Disordered Systems'', Cambridge University Press (1979) ISBN 0521292808.
+
*[http://dx.doi.org/10.1016/0031-8914(50)90072-3  L. van Hove, "Sur L'intégrale de Configuration Pour Les Systèmes De Particules À Une Dimension", Physica, '''16''' pp. 137-143 (1950)]
 +
*[http://dx.doi.org/10.1063/1.1699116 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)]
 +
*[http://dx.doi.org/10.1063/1.1699263 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)]
 +
*[http://dx.doi.org/10.3390/e10030248  Paolo V. Giaquinta "Entropy and Ordering of Hard Rods in One Dimension", Entropy '''10''' pp. 248-260 (2008)]
  
 
[[Category:Models]]
 
[[Category:Models]]
 
[[Category:Statistical mechanics]]
 
[[Category:Statistical mechanics]]

Revision as of 17:27, 14 December 2009

1-dimensional hard rods (sometimes known as a Tonks Gas [1]) consist of non-overlapping line segments of length \sigma who all occupy the same line which has length L. 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:

 \Phi_{12} (x_i,x_j) = \left\{ \begin{array}{lll} 0 & ; & |x_i-x_j| > \sigma \\
\infty &; & |x_i-x_j| < \sigma \end{array} \right.

where  \left. x_k \right. is the position of the center of the k-th rod, along with an external potential; the whole length of the rod must be inside the range:

 V_{0}(x_i) = \left\{ \begin{array}{lll} 0 & ; & \sigma/2 < x < L - \sigma/2 \\
\infty &; & {\mathrm {elsewhere}}. \end{array} \right.

Canonical Ensemble: Configuration Integral

The statistical mechanics of this system can be solved exactly. Consider a system of length  \left. L \right. defined in the range  \left[ 0, L \right] . The aim is to compute the partition function of a system of  \left. N \right. hard rods of length  \left. \sigma \right. . Consider that the particles are ordered according to their label:  x_0 < x_1 < x_2 < \cdots < x_{N-1} ; taking into account the pair potential we can write the canonical partition function (configuration integral) of a system of  N particles as:


\frac{ Z \left( N,L \right)}{N!} = \int_{\sigma/2}^{L+\sigma/2-N\sigma} d x_0 
\int_{x_0+\sigma}^{L+\sigma/2-N\sigma+\sigma} d x_1 \cdots 
\int_{x_{i-1}+\sigma}^{L+\sigma/2-N\sigma+i \sigma} d x_i \cdots 
\int_{x_{N-2}+\sigma}^{L+\sigma/2-N\sigma+(N-1)\sigma} d x_{N-1}.

Variable change:  \left. \omega_k = x_k - \left(k+\frac{1}{2}\right) \sigma \right.  ; we get:


\frac{ Z \left( N,L \right)}{N!} = \int_{0}^{L-N\sigma} d \omega_0 
\int_{\omega_0}^{L-N\sigma} d \omega_1 \cdots 
\int_{\omega_{i-1}}^{L-N\sigma} d \omega_i \cdots 
\int_{\omega_{N-2}}^{L-N\sigma} d \omega_{N-1}.

Therefore:


\frac{ Z \left( N,L \right)}{N!} =  \frac{ (L-N\sigma )^{N} }{N!}.

Q(N,L) = \frac{ (L-N \sigma )^N}{\Lambda^N N!}.

Thermodynamics

Helmholtz energy function

 \left. A(N,L,T) = - k_B T \log Q \right.

In the thermodynamic limit (i.e.  N \rightarrow \infty; L \rightarrow \infty with  \rho = \frac{N}{L} , remaining finite):

  A \left( N,L,T \right) = N k_B T \left[ \log \left( \frac{ N \Lambda} { L - N \sigma }\right)  - 1 \right].

Equation of state

Using the thermodynamic relations, the pressure (linear tension in this case)  \left. p \right. can be written as:


p = - \left( \frac{ \partial A}{\partial L} \right)_{N,T} =  \frac{ N k_B T}{L - N \sigma};

Z = \frac{p L}{N k_B T} = \frac{1}{ 1 - \eta},

where  \eta \equiv \frac{ N \sigma}{L} ; is the fraction of volume (i.e. length) occupied by the rods.

Isobaric ensemble: an alternative derivation

Adapted from Reference [2]. If the rods are ordered according to their label:  x_0 < x_1 < x_2 < \cdots < x_{N-1} the canonical partition function can also be written as:


Z=
\int_0^{x_1} d x_0
\int_0^{x_2} d x_1
\cdots
\int_0^{L} d x_{N-1}
f(x_1-x_0)
f(x_2-x_1)
\cdots
f(L-x_{N-1}),

where N! does not appear one would have N! analogous expressions by permuting the label of the (distinguishable) rods. f(x) is the Boltzmann factor of the hard rods, which is 0 if x<\sigma and 1 otherwise.

A variable change to the distances between rods:  y_k = x_k - x_{k-1} results in


Z =
\int_0^{\infty} d y_0
\int_0^{\infty} d y_1
\cdots
\int_0^{\infty} d y_{N-1}
f(y_1)
f(y_2)
\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 \sigma (as enforced by f(y)) and as long as they add up to L (as enforced by the Dirac delta). Writing the later as the inverse Laplace transform of an exponential:


Z =
\int_0^{\infty} d y_0
\int_0^{\infty} d y_1
\cdots
\int_0^{\infty} d y_{N-1}
f(y_1)
f(y_2)
\cdots
f(y_{N-1})
\frac{1}{2\pi i } \int_{-\infty}^{\infty} ds \exp \left[ - s \left(\sum_{i=0}^{N-1} y_i-L \right)\right].

Exchanging integrals and expanding the exponential the N integrals decouple:


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,


Z'(s)= \left\{ \int_0^{\infty} d y f(y) e^{ - s y } \right\}^N,

so that


Z'(s) = \int_0^{\infty} ds e^{ L s } Z(L).

This is precisely the transformation from the configuration integral in the canonical (N,T,L) ensemble to the isobaric (N,T,p) one, if one identifies s=p/k T. Therefore, the Gibbs energy function is simply G=-kT\log Z'(p/kT) , which easily evaluated to be G=kT N \log(p/kT)+p\sigma N. The chemical potential is \mu=G/N, and by means of thermodynamic identities such as \rho=\partial p/\partial \mu one arrives at the same equation of state as the one given above.

Confined hard rods

[3]

References

Related reading