Editing Solubility equilibrium (section)

=== Particle size effect ===
The thermodynamic solubility constant is defined for large monocrystals. Solubility will increase with decreasing size of solute particle (or droplet) because of the additional surface energy. This effect is generally small unless particles become very small, typically smaller than 1 μm. The effect of the particle size on solubility constant can be quantified as follows:
<math display="block">\log(^*K_{A}) = \log(^*K_{A \to 0}) + \frac{\gamma A_\mathrm{m}} {3.454RT}</math>
where *''K<sub>A</sub>'' is the solubility constant for the solute particles with the molar surface area ''A'', *''K''<sub>''A''→0</sub> is the solubility constant for substance with molar surface area tending to zero (i.e., when the particles are large), ''γ'' is the [[surface tension]] of the solute particle in the solvent, ''A''<sub>m</sub> is the molar surface area of the solute (in m<sup>2</sup>/mol), ''R ''is the [[universal gas constant]], and ''T'' is the [[absolute temperature]].<ref name=hefter>{{cite book|editor1-last=Hefter|editor1-first=G. T.|editor2-last=Tomkins|editor2-first=R. P. T.| title=The Experimental Determination of Solubilities |year=2003|publisher=Wiley-Blackwell |isbn= 0-471-49708-8 }}</ref>