## Abstract The calculation of phase diagrams for blends of linear and branched polymers made up of identical monomeric units is modeled using an approach that subdivides the mixing process into two steps: i) contact formation between the different components, keeping their chain conformations and
Polymer-Polymer Interaction: Consistent Modeling in Terms of Chain Connectivity and Conformational Response
โ Scribed by Bernhard A. Wolf
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 196 KB
- Volume
- 207
- Category
- Article
- ISSN
- 1022-1352
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โฆ Synopsis
Abstract
Summary: An approach developed for the modeling of polymer solutions is extended to polymer blends. It accounts explicitly for the fact that the segments of a given macromolecule cannot spread out over the entire volume of the system (chain connectivity) and that the space a polymer molecule occupies may change after contact formation between the components of a mixture (conformational response ฮถ). The validity of the equation obtained for the FloryโHuggins interaction parameter between polymers is tested by means of critical data published for the system PVME/PS. The measured phase diagrams can be modeled equally well by two limiting assumptions concerning the temperature dependence of the conformational response. However, using these two different sets of parameters to calculate the phase behavior for high molar masses of both polymers, leads to fundamental differences. One of them yields double critical points and predicts well defined critical compositions in the limit of infinite molar masses of both polymers, in contrast to the original FloryโHuggins theory. The physical meaning of the different parameters is analyzed and the composition and temperature dependencies of the FloryโHuggins interaction parameter resulting from the present modeling are compared with corresponding data reported in the literature.
Double critical line (double critical concentration ฯ~DC~ as a function of m and n) calculated by means of Equation (12) and (13) using the system specific parameters given in row two of Table 2, and its projections into the different planes.
imageDouble critical line (double critical concentration ฯ~DC~ as a function of m and n) calculated by means of Equation (12) and (13) using the system specific parameters given in row two of Table 2, and its projections into the different planes.
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