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Mean‐field‐theory for polymers in mixed solvents. Thermodynamic and structural properties
Author(s) -
Negadi Amina,
SansPennincks Anne,
Benmouna Mustapha,
Vilgis Thomas A.
Publication year - 1999
Publication title -
macromolecular theory and simulations
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.37
H-Index - 56
eISSN - 1521-3919
pISSN - 1022-1344
DOI - 10.1002/(sici)1521-3919(19990701)8:4<285::aid-mats285>3.0.co;2-w
Subject(s) - polymer , ternary operation , hamiltonian (control theory) , flory–huggins solution theory , criticality , thermodynamics , solvent , asymmetry , excluded volume , chemistry , solvent effects , statistical physics , materials science , physics , mathematics , organic chemistry , quantum mechanics , mathematical optimization , computer science , nuclear physics , programming language
Theoretical aspects of polymers in mixed solvents are considered using the Edwards Hamiltonian formalism. Thermodynamic and structural properties are investigated and some predictions are made when the mixed solvent approaches criticality. Both the single and the many chain problems are examined. When the mixed solvent is near criticality without solute, addition of a small amount of polymers shifts the criticality towards either enhanced compatibility or induced phase separation depending upon the value of the parameter describing the interaction asymmetry of the solvents with respect to the polymer. The polymer‐solvent effective interaction parameter increases strongly when the solvent mixture approaches criticality. Accordingly, the apparent excluded volume parameter decreases and may vanish or even become negative. Consequently, the polymer undergoes phase transition from a swollen state to an unperturbed state or even takes a collapsed configuration. The effective potential acting on a test chain in strong solutions is calculated and the concept of Edwards screening discussed. Structural properties of ternary mixtures of polymers in mixed solvents are investigated within the Edwards Hamiltonian model. It is shown that the effective potential on a test chain in strong solutions could be written as an infinite series expansion of terms describing interactions via one chain, two chains etc. This summation can be performed following a similar scheme as in the Ornstein‐Zernike series expansion.