Index of content:
Volume 40, Issue 2, June 2011
- REGULAR ARTICLES
40(2011); http://dx.doi.org/10.1063/1.3580290View Description Hide Description
The present review is dedicated to the velocity slip and temperature jump coefficients applied to modeling of gas flows. Such coefficients are used when a moderate gas rarefaction must be taken into account. In this case, calculations of gas flows can be performed on the basis of continuum mechanics equations applying the velocity slip and temperature jump boundary conditions. Thus, the velocity slip and temperature jump coefficients have the same importance in gas dynamics as the transport coefficients such as viscosity, thermal conductivity, and diffusion coefficients. A critical analysis of theoretical and experimental data on the slip and jump coefficients available in the open literature is presented in an accessible form so that it can be easily understandable for nonspecialists in rarefied gas dynamics. The most reliable results are selected and tabulated. The results cover a single gas with the complete and noncomplete accommodation on a solid surface, gaseous mixtures, and polyatomic gases. Many examples of applications of the slip and jump boundary conditions are given. The review will be useful as a reference for mathematicians, physicists, and engineers dealing with flows of moderately rarefied gases.
IUPAC-NIST Solubility Data Series. 90. Hydroxybenzoic Acid Derivatives in Binary and Ternary Systems. Part II. Hydroxybenzoic Acids, Hydroxybenzoates, and Hydroxybenzoic Acid Salts in Nonaqueous Systems40(2011); http://dx.doi.org/10.1063/1.3569816View Description Hide Description
The solid-liquid solubility data for well defined nonaqueous binary and ternary systems are reviewed. One component includes hydroxybenzoic acid, hydroxybenzoate, and hydroxybenzoic acid salt, and another component includes a variety of organic compounds (hydrocarbons, alcohols, halogenated hydrocarbons, carboxylic acids, esters, et al.) and carbon dioxide. The ternary systems include mixtures of organic substances of various classes and carbon dioxide. The total number of compilation sheets is 270 for six types of system. Almost all data are expressed as mass percent and mole fraction as well as the originally reported units, while some data are expressed as molar concentration. Critical evaluation was carried out for the binary nonaqueous systems of 2-, 3-, and 4-hydroxybenzoic acids and hydroxybenzoates (methylparaben, ethylparaben, propylparaben, and butylparaben) in alcohols, 1-heptane, and benzene.
40(2011); http://dx.doi.org/10.1063/1.3578343View Description Hide Description
Kinetic data published in the peer-reviewed literature over the period of 1988–2007 for radical reactions with molecules and ions derived from inorganic and organic solutes in aqueous solution have been critically reviewed. Rate constants for over 250 reactions, as studied by pulse radiolysis, end-product analysis, and other methods, have been tabulated.
40(2011); http://dx.doi.org/10.1063/1.3582533View Description Hide Description
A thermodynamic property formulation for dimethyl ether has been developed based on a selection of experimental thermodynamic property data. The formulation includes a fundamental equation, a vapor-pressure equation, and saturated-density equations for liquid and vapor states. In determining the coefficients of the equation of state, multiproperty fitting methods were used that included single-phase pressure-density-temperature , heat capacity,vapor pressure, and saturated density data. Deviations between experimental and calculated data are generally within the experimental accuracy. The equation of state has been developed to conform to the Maxwell criterion for two-phase liquid-vapor equilibrium states, and is valid for temperatures from the triple-point temperature to , with pressures up to and densities up to . The uncertainties of the equation of state in density are 0.1% for the liquid phase and 0.3% for the vapor phase. In the extended critical region, the uncertainties in density are 0.5%, except for very near the critical point. The uncertainties in vapor pressure are 0.2% above , and increase as temperature decreases. The uncertainties in saturated liquid density are 0.05%, except for near the critical point. The uncertainties in heat capacity are 2.0%. Detailed comparisons between the experimental data and calculated values are given.