@article {2556,
	title = {An Accurate Equation of State for Fluids and Solids},
	journal = {Journal of Physical Chemistry B},
	volume = {113},
	number = {35},
	year = {2009},
	note = {ISI Document Delivery No.: 487EETimes Cited: 0Cited Reference Count: 52Parsafar, G. A. Spohr, H. V. Patey, G. N.},
	month = {Sep},
	pages = {11977-11987},
	type = {Article},
	abstract = {A simple functional form for a general equation of state based on an effective near-neighbor pair interaction of an extended Lennard-Jones (12,6,3) type is given and tested against experimental data for a wide variety of fluids and solids, Computer simulation results for ionic liquids are used for further evaluation. For fluids, there appears to be no upper density limitation on the equation of state, The lower density limit for isotherms near the critical temperature is the critical density. The equation of state gives a good description of all types of fluids, nonpolar (including long-chain hydrocarbons), polar, hydrogen-bonded, and metallic, at temperatures ranging from the triple point to the highest temperature for which there is experimental data. For solids, the equation of state is very accurate for all types considered, including covalent, molecular, metallic, and ionic systems. The experimental pvT data available for solids does not reveal any pressure or temperature limitations. An analysis of the importance and possible underlying physical significance of the terms in the equation of state is given.},
	keywords = {400 DEGREES C, COMPRESSED LIQUIDS, DENSE FLUIDS, HIGH-PRESSURES, linear isotherm regularity, PVT PROPERTIES, SODIUM-CHLORIDE, TEMPERATURE, THERMODYNAMIC PROPERTIES, UNIVERSAL EQUATION},
	isbn = {1520-6106},
	url = {<Go to ISI>://000269252700022},
	author = {Parsafar, G. A. and Spohr, H. V. and Patey, G. N.}
}
@article {1258,
	title = {Fluctuation functions in aqueous NaCl and urea},
	journal = {Journal of Physical Chemistry B},
	volume = {109},
	number = {35},
	year = {2005},
	note = {ISI Document Delivery No.: 961UNTimes Cited: 4Cited Reference Count: 30},
	month = {Sep},
	pages = {16886-16890},
	type = {Article},
	abstract = {We earlier devised a set of fluctuation functions that provide relative qualitative differences of the amplitude (intensity) and the wavelength (extensity) of fluctuations in entropy and volume and the entropy-volume cross fluctuations. We discuss the mixing schemes in aqueous NaCl and urea using these fluctuation functions. Our earlier studies by using the second and third derivatives of Gibbs energy indicated that their effects on H2O are qualitatively different. An NaCl hydrates 7.5 molecules of H2O but leaves the bulk H2O away from the hydration shell unperturbed. Urea, on the other hand, connects onto the hydrogen bond network of H2O but retards the degree of fluctuation inherent in H2O. The behavior of the fluctuation functions calculated here are consistent with the above mixing schemes. Furthermore, urea was found to reduce the wavelength of fluctuation more strongly than NaCl.},
	keywords = {25-DEGREES-C, H2O, LIQUID WATER, MODEL, PARTIAL MOLAR FLUCTUATIONS, PERCOLATION, SODIUM-CHLORIDE, SYSTEMS, VOLUMETRIC PROPERTIES},
	isbn = {1520-6106},
	url = {<Go to ISI>://000231687400045},
	author = {Siu, D. and Koga,Yoshikata}
}
@article {4895,
	title = {Forces between like-charged walls in an electrolyte solution: A comparison of McMillan-Mayer results for several models},
	journal = {Journal of Chemical Physics},
	volume = {113},
	number = {7},
	year = {2000},
	note = {ISI Document Delivery No.: 344XYTimes Cited: 8Cited Reference Count: 28},
	month = {Aug},
	pages = {2851-2855},
	type = {Article},
	abstract = {The interaction of like-charged walls immersed in aqueous solutions with monovalent counterions is investigated at the McMillan-Mayer (MM) level of description. The net pressure acting between the walls is obtained by applying the anisotropic hypernetted-chain theory. The MM approach requires solvent-averaged ion-ion potentials of mean force as input. Results based on "realistic" models for Na+ and Cl- in water are available in the literature and these are used in the present calculations. The wall-wall interactions obtained can differ dramatically from the primitive model (dielectric continuum solvent) case. For some models attractive wall-wall forces are observed at small separations. The MM theory is found to be rather sensitive to details of the counterion-counterion potential of mean force, and different models for the same counterion can give qualitatively different results. At present it is difficult to evaluate the relative accuracy of the different models that have been proposed. However, the results presented here give at least an idea of the interesting possibilities that lie in the physically realistic range. (C) 2000 American Institute of Physics. [S0021-9606(00)50331-6].},
	keywords = {APPROXIMATION, DOUBLE-LAYER, FORCE, HARD-SPHERES, IMAGE INTERACTIONS, INHOMOGENEOUS COULOMB FLUIDS, MEAN, MOLECULAR-DYNAMICS, PLANAR SURFACES, SODIUM-CHLORIDE, WATER},
	isbn = {0021-9606},
	url = {<Go to ISI>://000088787400034},
	author = {Otto, F. and Patey, G. N.}
}
