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Vaporization transitions

This method is invalid because the temperature in the denominator of the equation must be the temperature at which the liquid-vapor transition is at equilibrium. Liquid water and water vapor at 1 atm pressure (standard state, indicated by ) are in equilibrium only at 100° C = 373 K. [Pg.491]

The liquid-vapor transition for H2O involves quite high evaporation enthalpy, which controls the thermal state of the system. [Pg.647]

Vaporization Transition Clausius-Clapeyron Equation For the liquid-vapor coexistence line ( vapor-pressure curve ), the Clapeyron equation (7.29) becomes... [Pg.222]

It is shown in this paper that, contrary to previous common belief, under certain special, but still fully feasible experimental conditions rarefaction shock waves can exist. In particular, this situation should certainly occur in gases with a sufficiently large specific heat e near the critical point of fluid-vapor transition. In recent years the prediction made by Ya.B. has been conclusively confirmed by experiment.1 Later Ya.B. considered the peculiarities of the state near the critical point which may occur in a rapid, shock expansion. [Pg.154]

A. Liquid-Vapor Transitions in One-Component Ionic Fluids... [Pg.6]

Apart from liquid-liquid transitions, liquid-vapor transitions in aqueous electrolyte solutions have played a crucial role in debates on ionic criticality [142-144], The liquid-vapor transition is usually associated with a mechanical instability with diverging density fluctuations, while liquid-liquid transitions are associated with a material instability with diverging concentration fluctuations. This requires, however, that both regimes are well-separated. Their interference can lead to complex phase behavior with continuous transitions from liquid-liquid demixing to liquid-gas condensation [9, 145, 146]. It is then not trivial to define the order parameter [147-149]. [Pg.22]

The continuous critical line for systems such as NaCl + H20 offers a temperature window for studying the behavior of electrolyte solutions near their liquid-vapor transition. Pitzer [4,13,142,144] compiled much evidence that the nonclassical fluctuations in pure water are apparently suppressed when adding electrolytes. Thus, from the application s point of view, a classical EOS may be quite useful. The pressing question is to what degree these observations withstand more quantitative analysis. [Pg.23]

While the early work on molten NH4CI gave only some qualitative hints that the effective critical behavior of ionic fluids may be different from that of nonionic fluids, the possibility of apparent mean-field behavior has been substantiated in precise studies of two- and multicomponent ionic fluids. Crossover to mean-field criticality far away from Tc seems now well-established for several systems. Examples are liquid-liquid demixings in binary systems such as Bu4NPic + alcohols and Na + NH3, liquid-liquid demixings in ternary systems of the type salt + water + organic solvent, and liquid-vapor transitions in aqueous solutions of NaCl. On the other hand, Pitzer s conjecture that the asymptotic behavior itself might be mean-field-like has not been confirmed. [Pg.26]

The transition to the continuum fluid may be mimicked by a discretization of the model choosing > 1. To this end, Panagiotopoulos and Kumar [292] performed simulations for several integer ratios 1 < < 5. For — 2 the tricritical point is shifted to very high density and was not exactly located. The absence of a liquid-vapor transition for = 1 and 2 appears to follow from solidification, before a liquid is formed. For > 3, ordinary liquid-vapor critical points were observed which were consistent with Ising-like behavior. Obviously, for finely discretisized lattice models the behavior approaches that of the continuum RPM. Already at = 4 the critical parameters of the lattice and continuum RPM agree closely. From the computational point of view, the exploitation of these discretization effects may open many possibilities for methodological improvements of simulations [292], From the fundamental point of view these discretization effects need to be explored in detail. [Pg.49]

Considering a liquid-vapor transition and I v ip Fliq. we get the approximate Clapeyron equation... [Pg.29]

Vinogradov (1964) divides the history of the atmosphere into three phases (Table 1) ancient (water vapor), transitional (nitrogen atmosphere), and present (oxysphere). Apparently the Precambrian BIF were deposited at the boundary of the transitional atmosphere and the oxysphere. Therefore, it is of particular interest to examine the evolution of the nitrogen atmosphere and its individual components, mainly nitrogen and carbon. [Pg.49]

Simulations of the RPM predict a phase transition for the RPM at low reduced temperature and low reduced density. It was difficult to localize because of the low figures of the critical data. By corresponding states arguments this critical point corresponds to the liquid/vapor transition of molten salts and to some liquid/liquid transitions in electrolyte solutions in solvents of low dielectric constant [23, 24],... [Pg.155]


See other pages where Vaporization transitions is mentioned: [Pg.1287]    [Pg.296]    [Pg.106]    [Pg.813]    [Pg.1663]    [Pg.94]    [Pg.16]    [Pg.16]    [Pg.151]    [Pg.419]    [Pg.89]    [Pg.169]    [Pg.817]    [Pg.7]    [Pg.109]    [Pg.156]    [Pg.165]    [Pg.181]   


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Clapeyron equation vaporization transition

Ionic fluid criticality liquid-vapor transition

Ising criticality liquid-vapor transition

Liquid-vapor phase transition critical point

Liquid-vapor phase transition molar Gibbs energy

Liquid-vapor transition

Liquids liquid-vapor phase transition

Phase transition solution-vapor

Phase transitions enthalpy of vaporization

Phase transitions liquid-vapor transition critical point

Phase transitions vaporization

Solid-Vapor Phase Transition

Solids solid-vapor phase transition

Thermodynamics liquid/vapor phase transition

Transition Metal Vapor Cryochemistry William J. Power and Geoffrey A. Ozin

Transition metal compounds, vapor pressure

Transition metal vapor cryochemistry

Transition metal vapor cryochemistry dinitrogen complexes

Transition metal vapor cryochemistry dioxygen complexes

Transition metal vapor cryochemistry in alkane matrices

Transition metal vapor cryochemistry nitrides

Transition metal vapor cryochemistry organic reactions

Transition metal vapor cryochemistry oxidative addition

Transition metal vapor cryochemistry polyolefin complexes

Transition metal vapor cryochemistry rearrangements

Transition metal vapor cryochemistry siloxanes

Transition metal vapor cryochemistry via photoselective aggregation

Transition, vapor-liquid-phase

Vapor + liquid equilibria, phase transitions

Vapor phase transition

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