The hierarchical reference theory as applied to square well fluids of variable range
نویسندگان
چکیده
Continuing our investigation into the numerical properties of the hierarchical reference theory, we study the square well fluid of range l from slightly above unity up to 3.6. After briefly touching upon the core condition and the related decoupling assumption necessary for numerical calculations, we shed some light on the way an inappropriate choice of the boundary condition imposed at high density may adversely affect the numerical results; we also discuss the problem of the partial differential equation becoming stiff for close-to-critical and subcritical temperatures. While agreement of the theory’s predictions with simulational and purely theoretical studies of the square well system is generally satisfactory for l*2, the combination of stiffness and the closure chosen is found to render the critical point numerically inaccessible in the current formulation of the theory for most of the systems with narrower wells. The mechanism responsible for some deficiencies is illuminated at least partially and allows us to conclude that the specific difficulties encountered for square wells are not likely to resurface for continuous potentials. © 2002 American Institute of Physics. @DOI: 10.1063/1.1483258#
منابع مشابه
Analytic Equation of State for the Square-well Plus Sutherland Fluid from Perturbation Theory
Analytic expressions were derived for the compressibility factor and residual internal energy of the square-well plus Sutherland fluid. In this derivation, we used the second order Barker-Henderson perturbation theory based on the macroscopic compressibility approximation together with an analytical expression for radial distribution function of the reference hard sphere fluid. These properties...
متن کاملPhase behavior of dipolar fluids from a modified statistical associating fluid theory for potentials of variable range.
A statistical associating fluid theory for potentials of variable range to model dipolar fluids is presented. The new theory, termed the SAFT-VR+D equation (the statistical associating fluid theory for potentials of variable range plus dipole), explicitly accounts for dipolar interactions and their effect on the structure of the fluid. This is achieved through the use of the generalized mean sp...
متن کاملirial coefficients and inversion curve of simple and associating fluids
Free energy simulation method is applied to calculate the virial coefficients of square-well (SW) fluids of variable well-width and square-well based dimer forming associating fluids. In this approach, Monte Carlo sampling is performed on a number of molecules equal to the order of integral, and configurations are weighted according to the absolute value of the integrand. An umbrella-sampling a...
متن کاملPhase behavior of dipolar associating fluids from the SAFT-VR+D equation of state.
The statistical associating fluid theory for potentials of variable range plus dipole (SAFT-VR+D) is extended to study associating dipolar fluids. In the SAFT-VR+D approach dipolar interactions are taken into account through the use of the generalized mean spherical approximation to describe a reference fluid of dipolar square-well segments. This enables the effect of the dipolar interactions o...
متن کاملA Modified van der Waals Mixture Theory for Associating Fluids: Application to Ternary Aqueous Mixtures
In this study a simple and general chemical association theory is introduced. The concept of infinite equilibrium model is re-examined and true mole fractions of associated species are calculated. The theory is applied to derive the distribution function of associated species. As a severe test the application of presented theory to the van der Waals mixture model is introduced in order to p...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2002