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However, when the ionic strength is changed the measured equilibrium constant will also change, so there is a need to estimate individual (single ion) activity coefficients. Debye–Hückel theory provides a means to do this, but it is accurate only at very low concentrations. Hence the need for an extension to Debye–Hückel theory.
By utilizing the interaction picture, one can use time-dependent perturbation theory to find the effect of H 1,I, [15]: 355ff e.g., in the derivation of Fermi's golden rule, [15]: 359–363 or the Dyson series [15]: 355–357 in quantum field theory: in 1947, Shin'ichirÅ Tomonaga and Julian Schwinger appreciated that covariant perturbation ...
For this assumption to be valid, equilibrium constants must be determined in a medium of relatively high ionic strength. Where this is not possible, consideration should be given to possible activity variation. The equilibrium expression above is a function of the concentrations [A], [B] etc. of the chemical species in equilibrium. The ...
A description of Debye–Hückel theory includes a very detailed discussion of the assumptions and their limitations as well as the mathematical development and applications. [5] A snapshot of a 2-dimensional section of an idealized electrolyte solution is shown in the picture. The ions are shown as spheres with unit electrical charge.
The equilibrium constant for a full redox reaction can be obtained from the standard redox potentials of the constituent half-reactions. At equilibrium the potential for the two half-reactions must be equal to each other and, of course, the number of electrons exchanged must be the same in the two half reactions. [32]
For example, if equilibrium is specified by a single chemical equation:, [24] ∑ j = 0 m ν j R j = 0 {\displaystyle \sum _{j=0}^{m}\nu _{j}R_{j}=0} where ν j is the stoichiometric coefficient for the j th molecule (negative for reactants, positive for products) and R j is the symbol for the j th molecule, a properly balanced equation will obey:
The equilibrium conditions are shown as curves on a curved surface in 3D with areas for solid, liquid, and vapor phases and areas where solid and liquid, solid and vapor, or liquid and vapor coexist in equilibrium. A line on the surface called a triple line is where solid, liquid and vapor can all coexist in equilibrium. The critical point ...
For example, potassium permanganate oxidations can be achieved by adding a catalytic quantity of a crown ether and a small amount of organic solvent to the aqueous reaction mixture, so that the oxidation reaction occurs in the organic phase. In all these examples, the ligand is chosen on the basis of the stability constants of the complexes formed.