Parameter used in predicting the
solubility of non-electrolytes (including polymers) in a given solvent.
For a substance

,
where
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is the molar energy of vaporization at zero pressure and
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is the molar volume.
Notes:
-
For a substance of low molecular weight, the value of the solubility parameter can be estimated most reliably from the enthalpy of vaporization and the molar volume.
-
The solubility of a substance B can be related to the square of the difference between the solubility parameters for supercooled liquid B and solvent at a given temperature, with appropriate
allowances for entropy of mixing. Thus, a value can be estimated from the solubility of the solid in a series of solvents of known solubility parameter. For a polymer, it is usually taken to be the value of the solubility parameter of the solvent producing the solution with maximum intrinsic viscosity or maximum swelling of a network of the polymer. See J.H. Hildebrand, R.L.Scott, The Solubility of Nonelectrolytes, 3rd ed., Reinhold Publishing (1950); Dover Publications (1964), Chap. VII, p.129; Chap.
XXIII, for the original definition, theory, and extensive examples.
-
The SI units are
,
but units used frequently are
or
,
where
.
The unit calorie is discouraged as obsolete.
Source:
PAC, 2008, 80, 233
(Glossary of terms related to solubility (IUPAC Recommendations 2008)) on page 264
This definition replaces an earlier definition of solubility parameter, δ.
Cite as:
IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by
A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997).
XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic,
J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8.
https://doi.org/10.1351/goldbook.