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The vapour pressure above the curved interface is then higher than that for the planar interface. This picture provides a simple conceptual basis for the Kelvin equation. The change in vapor pressure can be attributed to changes in the Laplace pressure. When the Laplace pressure rises in a droplet, the droplet tends to evaporate more easily.
the concentration of water may be taken as being constant and the formation of the hydronium ion is implicit. AH ⇌ A − + H + Water concentration is omitted from expressions defining equilibrium constants, except when solutions are very concentrated. = [] [] [] (K defined as a dissociation constant)
In the following table, material data are given with a pressure of 611.7 Pa (equivalent to 0.006117 bar). Up to a temperature of 0.01 °C, the triple point of water, water normally exists as ice, except for supercooled water, for which one data point is tabulated here. At the triple point, ice can exist together with both liquid water and vapor.
The potential density of a fluid parcel at pressure is the density that the parcel would acquire if adiabatically brought to a reference pressure , often 1 bar (100 kPa). Whereas density changes with changing pressure, potential density of a fluid parcel is conserved as the pressure experienced by the parcel changes (provided no mixing with ...
Partition coefficients can be measured experimentally in various ways (by shake-flask, HPLC, etc.) or estimated by calculation based on a variety of methods (fragment-based, atom-based, etc.). If a substance is present as several chemical species in the partition system due to association or dissociation, each species is assigned its own K ow ...
The relative activity of a species i, denoted a i, is defined [4] [5] as: = where μ i is the (molar) chemical potential of the species i under the conditions of interest, μ o i is the (molar) chemical potential of that species under some defined set of standard conditions, R is the gas constant, T is the thermodynamic temperature and e is the exponential constant.
Raoult's law (/ ˈ r ɑː uː l z / law) is a relation of physical chemistry, with implications in thermodynamics.Proposed by French chemist François-Marie Raoult in 1887, [1] [2] it states that the partial pressure of each component of an ideal mixture of liquids is equal to the vapor pressure of the pure component (liquid or solid) multiplied by its mole fraction in the mixture.
is the static pressure at the point at which pressure coefficient is being evaluated is the static pressure in the freestream (i.e. remote from any disturbance) is the freestream fluid density (Air at sea level and 15 °C is 1.225 /)