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Solubility will also depend on the excess or deficiency of a common ion in the solution [clarification needed], a phenomenon known as the common-ion effect. To a lesser extent, solubility will depend on the ionic strength of solutions. The last two effects can be quantified using the equation for solubility equilibrium.
In such cases involving strongly dipolar, slowly relaxing solvents, solvation of the transition state does not play a very large role in affecting the reaction rate. Instead, dynamic contributions of the solvent (such as friction, density, internal pressure, or viscosity) play a large role in affecting the reaction rate. [6] [9]
A sodium ion solvated by water molecules. Solvations describes the interaction of a solvent with dissolved molecules. Both ionized and uncharged molecules interact strongly with a solvent, and the strength and nature of this interaction influence many properties of the solute, including solubility, reactivity, and color, as well as influencing the properties of the solvent such as its ...
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 Hildebrand solubility parameter is the square root of the cohesive energy density: δ = Δ H v − R T V m . {\displaystyle \delta ={\sqrt {\frac {\Delta H_{v}-RT}{V_{m}}}}.} The cohesive energy density is the amount of energy needed to completely remove a unit volume of molecules from their neighbours to infinite separation (an ideal gas ).
The energy released by the solvation of the ammonium ions and nitrate ions is less than the energy absorbed in breaking up the ammonium nitrate ionic lattice and the attractions between water molecules. Dissolving potassium hydroxide is exothermic, as more energy is released during solvation than is used in breaking up the solute and solvent.
^ The enthalpy is the internal energy corrected for any pressure-volume work at constant (external) . We are not making any distinction here. This allows the approximation of Helmholtz free energy, which is the natural form of free energy from the Flory–Huggins lattice theory, to Gibbs free energy.
The Debye–Hückel theory [7] was based on the assumption that each ion was surrounded by a spherical "cloud" or ionic atmosphere made up of ions of the opposite charge. Expressions were derived for the variation of single-ion activity coefficients as a function of ionic strength. This theory was very successful for dilute solutions of 1:1 ...