Solubility properties in polymers and biological media: 10. The solubility of gaseous solutes in polymers, in terms of solute-polymer interactions

Michael H. Abraham, Priscilla L. Grellier, R. Andrew McGill, Ruth M. Doherty, Mortimer J. Kamlet, Thomas N. Hall, Robert W. Taft, Peter W. Carr, William J. Koros

Research output: Contribution to journalArticlepeer-review

29 Scopus citations

Abstract

A general equation. SP=SP0+l log L16+s(π2*+dδ2) + aα2 + bβ2. has been used to describe solubility properties of a wide range of gaseous solutes in polymers. The property, SP, may be a log VG value, an enthalpy of solution, etc., and the explanatory variables are solute parameters: L16 is the Ostwald solubility coefficient of the solute on hexadecane at 25°C, π*2 is the solute dipolarity, δ2 a polarizability correction term, α2 the solute hydrogen-bond acidity, and β2 the solute hydrogen-bond basicity. Solubilities may then be discussed in terms of the various solute-solvent interactions that are reflected by the coefficients of the various terms. These are cavity effects and dispersion forces (l), dipole-dipole and dipole-induced-dipole interactions (s), and hydrogen-bonding between solute acid and polymer base (a) or between solute base and polymer acid (b). For non-dipolar solutes in all non-aqueous solvent phases, and for weakly dipolar solutes in weakly dipolar phases, the general equation reduces to a more specific equation that includes only the term due to cavity effects and dispersion forces. SP=SP0+l log L16.

Original languageEnglish (US)
Pages (from-to)1363-1369
Number of pages7
JournalPolymer
Volume28
Issue number8
DOIs
StatePublished - Jul 1987

Keywords

  • hydrogen-bonding
  • poly(ethylene oxide)
  • poly(methyl methacrylate)
  • poly(vinyl acetate)
  • polymer-solute interactions

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