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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.
The dependence on temperature of solubility for an ideal solution (achieved for low solubility substances) is given by the following expression containing the enthalpy of melting, Δ m H, and the mole fraction of the solute at saturation: () = ¯,, where ¯, is the partial molar enthalpy of the solute at infinite dilution and , the enthalpy ...
However, for aqueous solutions, the Henry's law solubility constant for many species goes through a minimum. For most permanent gases, the minimum is below 120 °C. Often, the smaller the gas molecule (and the lower the gas solubility in water), the lower the temperature of the maximum of the Henry's law constant.
Salting in refers to the effect where increasing the ionic strength of a solution increases the solubility of a solute, such as a protein. This effect tends to be observed at lower ionic strengths. [citation needed] Protein solubility is a complex function of physicochemical nature of the protein, pH, temperature, and the concentration of the ...
This is the minimum temperature the solution must be at to allow the surfactant to precipitate into aggregates. [8] Below this temperature no level of solubility will be sufficient to precipitate aggregates due to minimal movement of particles in solution. [8] The Krafft Temperature (T k) is based on the concentration of counter-ions (C aq). [8]
The temperature of the solution eventually decreases to match that of the surroundings. The equilibrium, between the gas as a separate phase and the gas in solution, will by Le Châtelier's principle shift to favour the gas going into solution as the temperature is decreased (decreasing the temperature increases the solubility of a gas).
It can be calculated as K b = RT b 2 M/ΔH v, where R is the gas constant, and T b is the boiling temperature of the pure solvent [in K], M is the molar mass of the solvent, and ΔH v is the heat of vaporization per mole of the solvent.
The phase behavior of polymer solutions is an important property involved in the development and design of most polymer-related processes. Partially miscible polymer solutions often exhibit two solubility boundaries, the upper critical solution temperature (UCST) and the LCST, both of which depend on the molar mass and the pressure. At ...