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When the electrode is calibrated with solutions of known concentration, by means of a strong acid–strong base titration, for example, a modified Nernst equation is assumed. E = E 0 + s log 10 [ A ] {\displaystyle E=E^{0}+s\log _{10}\mathrm {[A]} }
Most commonly, a solution containing the metal ion and the ligand in a medium of high ionic strength is first acidified to the point where the ligand is fully protonated. This solution is then titrated , often by means of a computer-controlled auto-titrator, with a solution of CO 2 -free base.
In electrochemistry, the Nernst equation is a chemical thermodynamical relationship that permits the calculation of the reduction potential of a reaction (half-cell or full cell reaction) from the standard electrode potential, absolute temperature, the number of electrons involved in the redox reaction, and activities (often approximated by concentrations) of the chemical species undergoing ...
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.
It is slightly soluble in water (with solubility product K sp = 2.36×10 −6 at 25 °C) [13] as well as dilute hydrofluoric acid, giving a pale green solution. [1] It is insoluble in organic solvents. [5] The tetrahydrate can be prepared by dissolving iron in warm hydrated hydrofluoric acid and precipitating the result by addition of ethanol. [1]
Indeed, for ideal-gas reactions K p is independent of pressure. [17] Pressure dependence of the water ionization constant at 25 °C. In general, ionization in aqueous solutions tends to increase with increasing pressure. In a condensed phase, the pressure dependence of the equilibrium constant is associated with the reaction volume. [18] For ...
In thermodynamics, an activity coefficient is a factor used to account for deviation of a mixture of chemical substances from ideal behaviour. [1] In an ideal mixture, the microscopic interactions between each pair of chemical species are the same (or macroscopically equivalent, the enthalpy change of solution and volume variation in mixing is zero) and, as a result, properties of the mixtures ...
The partial volume of a particular gas is a fraction of the total volume occupied by the gas mixture, with unchanged pressure and temperature. In gas mixtures, e.g. air, the partial volume allows focusing on one particular gas component, e.g. oxygen.