6533b7d2fe1ef96bd125e00e

RESEARCH PRODUCT

Interfacial tension between polymer-containing liquids - Predictability and influences of additives

Bernhard A. Wolf

subject

chemistry.chemical_classificationChromatographyPolymers and PlasticsOrganic ChemistryMixing (process engineering)ThermodynamicsPolymerCondensed Matter PhysicsGibbs free energySurface tensionchemistry.chemical_compoundsymbols.namesakeMonomerchemistryMaterials ChemistryCopolymersymbolsPolymer blendTie line

description

The first part of the contribution deals with the interfacial tension, σ, of phase-separated polymer solutions in single or mixed solvents and of binary polymer blends as a function of the relative distance to the critical temperature of the system, special attention being paid to the possibilities of theoretical prediction. Two methods are discussed in more detail. One is based on a realistic description of the Gibbs energy of mixing as a function of composition, the second correlates σ with the length of the measured tie line. The second part is devoted to another aspect, namely the effects of additives on the interfacial tension between the coexisting phases of demixed polymer solutions and between highly incompatible polymers. In the former case, it is demonstrated that an addition of a thermodynamically good solvent is normally associated with a reduction in σ; however, adding a high-molecular-weight compound which is incompatible with the dissolved polymer leads to an increase in σ, The interfacial tension between incompatible homopolymers is efficiently reduced by block copolymers consisting of monomeric units which are either identical with or different from those of the homopolymers; in contrast to theoretical expectation, the molecular architecture of the additives seems to be of minor importance only. Random copolymers which are insoluble in the homopolymers can also efficiently reduce the interfacial tension.

https://doi.org/10.1002/masy.19991390110