Simulations based on Cahn-Hilliard spinodal decomposition theory for phase separation in thermally quenched polymer/solvent/nonsolvent systems are presented. Two common membrane-forming systems are studied, cellulose acetate [CA]/ acetone/water, and poly(ethersulfone) [PES]/dimethylsulfoxide [DMSO]/
Theoretical Modeling of the Phase Separation Dynamics in Blends of Reactive Monomers
✍ Scribed by Gregory R. Yandek; Thein Kyu
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 318 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1022-1344
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✦ Synopsis
Abstract
Summary: Experimental observations of the dynamics of phase behavior for blends of reactive constituents, i.e. diglycidyl ether of bisphenol A (DGEBA), curing agent methylene dianiline (MDA), and a reactive liquid rubber (R45EPI), have been theoretically modeled by coupling system thermodynamics governed by a summation of the free energies of mixing and network elasticity with reaction kinetics and diffusion equations. Snap‐shots of the temporal evolution of ternary phase diagrams have been established based on the self‐condensation reactions of DGEBA‐MDA and R45EPI as well as a cross‐reaction between the two constituents forming a copolymer. Numerical solution of the proposed mean‐field model provides good qualitative agreement with experimental results, namely, the observance of phase separation followed by a phase dissolution and subsequent secondary segregation in a 50/25.4/50 DGEBA/MDA/R45EPI mixture, as well as a single gradual phase separation in a 70/25.4/30 mixture. The phase separation dynamics are explained by a competition between the growth in molecular weights of the reactive species rendering the systems towards instability, and the formation of copolymer acting to compatibilize the mixtures.
Theoretical phase diagram for a DGEBA/MDA/R45EPI system.
magnified imageTheoretical phase diagram for a DGEBA/MDA/R45EPI system.
📜 SIMILAR VOLUMES
## Abstract The properties of the model B of mesoscopic dynamic with the Flory–Huggins free energy for the homopolymer blend are discussed. We focus on the rescaling of the spatial coordinates in the model and demonstrate that the commonly used rescaling of the spatial coordinates by the function v
## Abstract **Summary:** A model system, consisting of a linear polymer dissolved in a bifunctional monomer/co‐monomer solvent, was selected to test the applicability of the Flory‐Huggins (FH) theory in the absence of the usual assumptions present in the analysis of modified thermosetting polymers.
Using nuclear reaction analysis composition-depth profiling, we investigate the influence of symmetric/asymmetric confining walls on the equilibrium configuration of thin films of phase-separated polymer blends. Depth profiles of samples annealed under symmetric boundary conditions show a laterally