@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 {1604,
	title = {Novel method of measuring heat capacity of supercritical fluid using Peltier elements},
	journal = {Japanese Journal of Applied Physics Part 1-Regular Papers Brief Communications \& Review Papers},
	volume = {45},
	number = {1A},
	year = {2006},
	note = {ISI Document Delivery No.: 009YXTimes Cited: 2Cited Reference Count: 9},
	month = {Jan},
	pages = {269-273},
	type = {Article},
	abstract = {We present a simple and convenient method of measuring the heat capacity of a fluid sample at a high pressure. A heat-flux-type calorimeter containing a sample cell with a thin wall and small holes is placed in a high-pressure vessel filled with the fluid sample itself. A thermoelectric module serves as the heat pump and heat flow sensor by taking advantage of the Peltier and Seebeck effects, respectively. To obtain the total heat transferred from the measured raw data, we employ a new estimation technique with a least-squares method. The performance of the method is examined by the measurement of supercritical CO2. The temperature increase necessary for the measurement can be suppressed to less than 40 mK; such a small amount scarcely disturbs the state for a temperature- sensitive sample. This method is suitable for determining the heat capacities of supercritical fluids including the states relatively close to a critical point.},
	keywords = {CALORIMETER, CARBON-DIOXIDE, CO2, heat capacity, HIGH-PRESSURES, Peltier element, POINT, STATE, supercritical fluid, THERMAL-CONDUCTIVITY MEASUREMENT},
	isbn = {0021-4922},
	url = {<Go to ISI>://000235150700062},
	author = {Tozaki, K. and Kido, Y. and Koga,Yoshikata and Nishikawa, K.}
}
@article {4897,
	title = {Measurements of Mu+NO termolecular kinetics up to 520 bar: isotope effects and the Troe theory},
	journal = {Physical Chemistry Chemical Physics},
	volume = {2},
	number = {4},
	year = {2000},
	note = {ISI Document Delivery No.: 281JDTimes Cited: 3Cited Reference Count: 58},
	pages = {621-629},
	type = {Article},
	abstract = {The recombination reaction Mu + NO + MMuNO + M (M = He, N-2, CH4) has been studied by the muon spin relaxation/rotation (mu SR) technique up to 520 bar at room temperature. The reaction remains in the low pressure regime throughout. The measured termolecular addition rate constant in N-2, 8.8 +/- 0.3 x 10(-33) cm(6) s(-1), is essentially the same as that found in our earlier study at pressures below 60 bar [J. J. Pan et al., J. Phys. Chem., 1995, 99, 17160]. It is somewhat smaller in He, 7.7 +/- 1.0 x 10(-33), but larger in CH4, 12.8 +/- 2.0 x 10(-33). The Mu + NO reaction is about five times slower than the corresponding H + NO reaction. The strong collision limits of the rate constants for three H-isotopes (Mu, H, D) reacting with NO have been estimated with Troe{\textquoteright}s formalism for unimolecular dissociation in the low pressure regime, based on the ab initio potential energy surface of Guadagnini et al. [J. Chem. Phys., 1995, 102, 774]. The Troe calculations give less than satisfactory agreement with experiment with the corresponding weak collision factor, beta(c), higher than expected by a factor of similar to 2 for H + NO. The calculated kinetic isotope effect in the strong collision limit for Mu/H is weaker than the measured effect by a factor of two giving an apparent large isotope effect in this factor, beta(c)(Mu) approximate to 1/2,beta(o)(H), possibly due to mode specific collisional stabilization.},
	keywords = {COLLISIONAL ENERGY-TRANSFER, DISSOCIATION, ELECTRON-SPIN EXCHANGE, GAS-PHASE, HIGH-PRESSURES, HNO, muonium, RATE CONSTANTS, relaxation, THERMAL UNIMOLECULAR REACTIONS},
	isbn = {1463-9076},
	url = {<Go to ISI>://000085154400025},
	author = {Pan, J. J. and Arseneau, D. J. and Senba, M. and Fleming, Donald G. and Himmer, U. and Suzuki, Y.}
}
