TY - JOUR
T1 - The isotropic-nematic phase transition in uniaxial hard ellipsoid fluids
T2 - Coexistence data and the approach to the Onsager limit
AU - Camp, Philip J.
AU - Mason, Carl P.
AU - Allen, Michael P.
AU - Khare, Anjali A.
AU - Kofke, David A.
PY - 1996/8/15
Y1 - 1996/8/15
N2 - The isotropic-nematic (I-N) phase transition in hard ellipsoid fluids has been studied by computer simulation, using the Gibbs-Duhem integration technique introduced by Kofke; and theoretically, using Onsager theory and the Parsons-Lee improvement. In the simulations, the I-N coexistence line is mapped out in the P-x plane, where P is the pressure and x is the elongation, by numerically integrating a Clapeyron-like first-order differential equation, using constant-pressure simulation data for the two coexisting phases. The elongation range 5≤x≤20 has been studied, using independent starting points provided by chemical potential calculations and thermodynamic integration of the equation of state at x = 5,20, plus a direct Gibbs ensemble simulation at x = 20. The Onsager-Parsons-Lee theory has been applied to the I-N phase transition for aspect ratios up to x = 1000, affording an accurate investigation of the approach to the Onsager limit for this model. This involved the numerical computation of the orientation-dependent second virial coefficient in a way that avoids expansions in Legendre polynomials, so as to be accurate at high elongation. Over the elongation range studied here, agreement between simulation and the Parsons-Lee theory is good.
AB - The isotropic-nematic (I-N) phase transition in hard ellipsoid fluids has been studied by computer simulation, using the Gibbs-Duhem integration technique introduced by Kofke; and theoretically, using Onsager theory and the Parsons-Lee improvement. In the simulations, the I-N coexistence line is mapped out in the P-x plane, where P is the pressure and x is the elongation, by numerically integrating a Clapeyron-like first-order differential equation, using constant-pressure simulation data for the two coexisting phases. The elongation range 5≤x≤20 has been studied, using independent starting points provided by chemical potential calculations and thermodynamic integration of the equation of state at x = 5,20, plus a direct Gibbs ensemble simulation at x = 20. The Onsager-Parsons-Lee theory has been applied to the I-N phase transition for aspect ratios up to x = 1000, affording an accurate investigation of the approach to the Onsager limit for this model. This involved the numerical computation of the orientation-dependent second virial coefficient in a way that avoids expansions in Legendre polynomials, so as to be accurate at high elongation. Over the elongation range studied here, agreement between simulation and the Parsons-Lee theory is good.
UR - http://www.scopus.com/inward/record.url?scp=0001443834&partnerID=8YFLogxK
U2 - 10.1063/1.472146
DO - 10.1063/1.472146
M3 - Article
AN - SCOPUS:0001443834
SN - 0021-9606
VL - 105
SP - 2837
EP - 2849
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 7
ER -