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Tricritical points in bimodal polymer solutions
Author(s) -
Igal Szleifer,
Gerrit ten Brinke
Publication year - 1996
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.471295
Subject(s) - cyclohexane , polymer , tricritical point , polystyrene , chain (unit) , materials science , polymer chemistry , thermodynamics , solvent , chemistry , physics , organic chemistry , quantum mechanics , composite material , phase (matter) , phase diagram
The tricritical point of polymer solutions composed by two polymer homologs of different molecular weight in a solvent is studied using the single-chain mean-field theory. The tricritical point is found for a ratio of molecular weights of the two polymers r=N-1/N-2, which decreases as a function of the short chain length N-2 from 51 to approximately 40 for N-2 increasing from 1 to 8. This last value is still much larger than the experimentally measured value for mixtures of polystyrene in cyclohexane, where it was found that r similar or equal to 25. Although a further reduction of r as a function of N-2 seems likely, the chain lengths of the corresponding long chains are beyond the reliability limit of the SAW's simulation involved. The addition of a small effective repulsion between the polymer homologs, is found to bring down the predicted value to 25. (C) 1996 American Institute of Physics

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