Small colloids in a uni-univalent aqueous electrolyte are modeled by a four-component solvent primitive model. The symmetric Poisson-Boltzmann theory is used to analyze the system and to calculate the second virial coefficient B2 of very dilute particle suspensions for varying solute and solvent concentrations. The results are compared with some experimental results on B2 of the silicotungstate...

A general method for modeling macromolecular shape in solution is described involving measurements of viscosity, radius of gyration, and the second thermodynamic virial coefficient. The method, which should be relatively straightforward to apply, does not suffer from uniqueness problems, involves shape functions that are independent of hydration, and models the gross conformation of the macromo...

A simple extension of existing models for protein crystallisation is described, in which salt ions and charge neutrality are explicitly incorporated. This provides a straightforward explanation for the shape of protein crystallisation boundaries, the associated scaling properties seen for lysozyme, and can also explain much of the salt dependence of the second virial coefficient. The analysis h...

A method is presented for determining second virial coefficients (B(2)) of protein solutions from retention time measurements in size exclusion chromatography. We determine B(2) by analyzing the concentration dependence of the chromatographic partition coefficient. We show the ability of this method to track the evolution of B(2) from positive to negative values in lysozyme and bovine serum alb...

Numerous scientific and industrial situations require thermodynamic properties of gas mixtures containing water. Examples include the development of humidity standards (where the dominant correction is the nonideality of water in the vapor phase) and design calculations for the utilization of synthesis and combustion gases in advanced power-generation cycles. In many of these cases, the conditi...

in the present work, we have examined the ability of some different equations of state in predicting the joule-thomson coefficient, ?j-t, of different fluids. for dense fluids, for which density is greater than the boyle density, ?b, two appropriate equations of state, namely the linear isotherm regularity, lir, and the dense system equation of state, dseos, have been examined. the results show...

To get a mole of a gas, it is necessary to calculate the intermolecular interaction. Theseintermolecular interactions can be depicted by drawing the potential energy of a pair molecule inrelation to the distance. The intermolecular potential energy surface in the mixtures of CH4-H2COgases from ab initio calculations has been explored. In ab initio calculations the basis setsuperposition error (...