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Now, invoking the condition that the system is in equilibrium, that is, the chemical potential of the adsorbed molecules is equal to that of the molecules in gas phase, we have An example plot of the surface coverage θ A = P/(P + P 0) with respect to the partial pressure of the adsorbate. P 0 = 100 mTorr.
This dependence on microscopic variables is the central point of statistical mechanics. With a model of the microscopic constituents of a system, one can calculate the microstate energies, and thus the partition function, which will then allow us to calculate all the other thermodynamic properties of the system.
The term bond-dissociation energy is similar to the related notion of bond-dissociation enthalpy (or bond enthalpy), which is sometimes used interchangeably.However, some authors make the distinction that the bond-dissociation energy (D 0) refers to the enthalpy change at 0 K, while the term bond-dissociation enthalpy is used for the enthalpy change at 298 K (unambiguously denoted DH° 298).
For example, such a regulation might limit the concentration of NOx to 55 ppmv in a dry combustion exhaust gas corrected to 3 volume percent O 2. As another example, a regulation might limit the concentration of particulate matter to 0.1 grain per standard cubic foot (i.e., scf) of dry exhaust gas corrected to 12 volume percent CO 2.
In simple words, we can say that the partial pressure of a gas in vapour phase is directly proportional to the mole fraction of a gas in solution. An example where Henry's law is at play is the depth-dependent dissolution of oxygen and nitrogen in the blood of underwater divers that changes during decompression , going to decompression sickness .
In gas dynamics we are interested in the local relations between pressure, density and temperature, rather than considering a fixed quantity of gas. By considering the density ρ = M / V {\displaystyle \rho =M/V} as the inverse of the volume for a unit mass, we can take ρ = 1 / V {\displaystyle \rho =1/V} in these relations.
K a is variously named a dissociation constant, [3] an acid ionization constant, [2]: 668 an acidity constant [1] or an ionization constant. [ 2 ] : 708 It serves as an indicator of the acid strength: stronger acids have a higher K a value (and a lower p K a value).
In real world applications, complete combustion does not typically occur. Chemistry dictates that dissociation and kinetics will change the composition of the products. There are a number of programs available that can calculate the adiabatic flame temperature taking into account dissociation through equilibrium constants (Stanjan, NASA CEA, AFTP).