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RESEARCH PRODUCT

Random Copolymers:  Their Solution Thermodynamics as Compared with That of the Corresponding Homopolymers

Maria BerceaAnd John EckeltBernhard A. Wolf

subject

Materials scienceVapor pressureGeneral Chemical EngineeringMethyl acetateAnalytical chemistryGeneral ChemistryFlory–Huggins solution theoryIndustrial and Manufacturing EngineeringStyrenechemistry.chemical_compoundMonomerchemistryPolymer chemistryCopolymerPolystyreneMethyl methacrylate

description

Vapor pressure data (at 50 °C) of solutions of poly(methyl methacrylate) [PMMA], polystyrene [PS], and poly(styrene-ran-methyl methacrylate) [P(S-ran-MMA)], with different weight fractions f of styrene units, in either CHCl3, acetone [AC], methyl acetate [MeAc], or toluene [TL] were evaluated with respect to the dependence of the Flory−Huggins interaction parameter χ on polymer concentration and on f. For all solutions under investigation, χ varies considerably with the composition of the mixture, and only for four of them [CHCl3/PS, AC/PMMA, MeAc/PS, and TL/P(S-ran-MMA) f = 0.5] is this dependence linear; another four systems exhibit a minimum [CHCl3/PMMA, CHCl3/P(S-ran-MMA) f = 0.5, TL/PMMA, and TL/PS], and only one [MeAc/PMMA] shows a maximum. With the exception of CHCl3/P(S-ran-MMA) and f = 0.5, the χ values of the copolymers do not fall reasonably between the data obtained for the corresponding homopolymers. In most cases, the incorporation of a small fraction of the monomer that interacts less favor...

https://doi.org/10.1021/ie0716619