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Table data obtained from CRC Handbook of Chemistry and Physics, 44th ed. log 10 of ethylene vapor pressure. Uses formula: ...
Valid results within the quoted ranges from most equations are included in the table for comparison. A conversion factor is included into the original first coefficients of the equations to provide the pressure in pascals (CR2: 5.006, SMI: -0.875).
Table data obtained from CRC Handbook of Chemistry and Physics, 44th ed. Temperature dependence of ethylene glycol vapor pressure. Uses formula ...
This causes severe problems for computational techniques which rely on a continuous vapor pressure curve. Two solutions are possible: The first approach uses a single Antoine parameter set over a larger temperature range and accepts the increased deviation between calculated and real vapor pressures.
The work done in a process on vapor cycles is represented by length of h, so it can be measured directly, whereas in a T–s diagram it has to be computed using thermodynamic relationship between thermodynamic properties. [1] In an isobaric process, the pressure remains constant, so the heat interaction is the change in enthalpy. [2]
This is illustrated in the vapor pressure chart (see right) that shows graphs of the vapor pressures versus temperatures for a variety of liquids. [7] At the normal boiling point of a liquid, the vapor pressure is equal to the standard atmospheric pressure defined as 1 atmosphere, [1] 760 Torr, 101.325 kPa, or 14.69595 psi.
J.A. Dean (ed.), Lange's Handbook of Chemistry (15th Edition), McGraw-Hill, 1999; Section 6, Thermodynamic Properties; Table 6.4, Heats of Fusion, Vaporization, and Sublimation and Specific Heat at Various Temperatures of the Elements and Inorganic Compounds
DePriester Charts provide an efficient method to find the vapor-liquid equilibrium ratios for different substances at different conditions of pressure and temperature. The original chart was put forth by C.L. DePriester in an article in Chemical Engineering Progress in 1953.