Search results
Results from the WOW.Com Content Network
If the pressure is increased by the addition of an inert gas, then neither the composition at equilibrium nor the equilibrium constant are appreciably affected (because the partial pressures remain constant, assuming an ideal-gas behaviour of all gases involved). However, the composition at equilibrium will depend appreciably on pressure when:
The limitations arise because the Nernst equation breaks down at very low or very high pH. When a glass electrode is used to obtain the measurements on which the calculated equilibrium constants depend, the precision of the calculated parameters is limited by secondary effects such as variation of liquid junction potentials in the electrode. In ...
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.
In contrast, the concentration does change with , since the density of a solution and thus its volume are temperature-dependent. Defining the aqueous-phase composition via molality has the advantage that any temperature dependence of the Henry's law constant is a true solubility phenomenon and not introduced indirectly via a density change of ...
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 ...
where p A is the partial pressure of A over the surface, [S] is the concentration of free sites in number/m 2, [A ad] is the surface concentration of A in molecules/m 2 (concentration of occupied sites), and k ad and k d are constants of forward adsorption reaction and backward desorption reaction in the above reactions.
However, the van der Waals equation, based on a mean-field theory, does not hold near the critical point. In particular, it predicts wrong scaling laws . To analyse properties of fluids near the critical point, reduced state variables are sometimes defined relative to the critical properties [ 15 ]
In fluid dynamics, the pressure coefficient is a dimensionless number which describes the relative pressures throughout a flow field. The pressure coefficient is used in aerodynamics and hydrodynamics. Every point in a fluid flow field has its own unique pressure coefficient, C p.