How is the saturated vapor pressure calculated in the property tables for pure substances?
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The table “900 Tables of Physical Properties of Pure Substances ChemPPDB_CC_Hgbbs” downloaded from the Internet allows for the calculation of saturated vapor pressure at different temperatures; however, when different pressures are entered, the saturated vapor pressure remains unchanged. Is there something wrong with this table?
I am in a hurry to calculate the saturated vapor pressure of substances at the same temperature but different pressures. Could you advise me on any other software or tables that I can use?
The saturated vapor pressure is dependent on temperature. What happens when the parameter \"pressure\" is entered? If a closed system contains not only component A which is under study but also component B, then the pressure of B has no effect on the partial pressure of A; the pressure in its equilibrium state will be equal to its saturated vapor pressure. With one exception: if the concentration of A in the liquid phase is not 100%, then its partial pressure is equal to its saturated vapor pressure multiplied by the percentage of the liquid phase
May I ask, in a closed container, is the saturated vapor pressure independent of pressure?
In a closed container, does the saturated vapor pressure of a single component remain unchanged under pressures of 1 kilogram and 10 kilograms?
According to Antonie’s equation, the saturated vapor pressure of a pure substance is a function of temperature; the saturated vapor pressures at different pressures and for different substances are not the same thing
It has nothing to do with pressure; it depends only on temperature and the composition of the liquid phase. The amount of N2 in a sealed container is independent of other volatile components