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Values are given in terms of temperature necessary to reach the specified pressure. 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).
Propylene oxide is an extremely flammable liquid, and its vapors can form explosive mixtures with air at concentrations as low as 2.3% (Lower Explosive Limit). [25] Propylene oxide vapor is twice as dense as air.
A Assuming an altitude of 194 metres above mean sea level (the worldwide median altitude of human habitation), an indoor temperature of 23 °C, a dewpoint of 9 °C (40.85% relative humidity), and 760 mmHg sea level–corrected barometric pressure (molar water vapor content = 1.16%). B Calculated values *Derived data by calculation.
where p is the vapor pressure, ... Water 8.07131: 1730.63: 233.426: 1: 100 ... Calculation of vapor pressures with the Antoine equation
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Vapor pressure [a] or equilibrium vapor pressure is the pressure exerted by a vapor in thermodynamic equilibrium with its condensed phases (solid or liquid) at a given temperature in a closed system. The equilibrium vapor pressure is an indication of a liquid's thermodynamic tendency to evaporate.
In that context, a lighter component means a component with a lower boiling point (or a higher vapor pressure) and a heavier component means a component with a higher boiling point (or a lower vapor pressure). Thus, for the distillation of any multi-component mixture, the relative volatility is often defined as
Let K 0 is the normal conductivity at one bar (10 5 N/m 2) pressure, K e is its conductivity at special pressure and/or length scale. Let d is a plate distance in meters, P is an air pressure in Pascals (N/m 2 ), T is temperature Kelvin, C is this Lasance constant 7.6 ⋅ 10 −5 m ⋅ K/N and PP is the product P ⋅ d/T .