Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Polymer brushes numerical self-consistent field

A successful theoretical description of polymer brushes has now been established, explaining the morphology and most of the brush behavior, based on scaling laws as developed by Alexander [180] and de Gennes [181]. More sophisticated theoretical models (self-consistent field methods [182], statistical mechanical models [183], numerical simulations [184] and recently developed approaches [185]) refined the view of brush-type systems and broadened the application of the theoretical models to more complex systems, although basically confirming the original predictions [186]. A comprehensive overview of theoretical models and experimental evidence of polymer bmshes was recently compiled by Zhao and Brittain [187] and a more detailed survey by Netz and Adehnann [188]. [Pg.400]

Figure 6.13. The height of a polymer brush in a chemically identical matrix of equal degree of polymerisation 1000 as predicted by the scaling theory and calculated by the numerical self-consistent mean-field method. The SCF calculations were done using a... Figure 6.13. The height of a polymer brush in a chemically identical matrix of equal degree of polymerisation 1000 as predicted by the scaling theory and calculated by the numerical self-consistent mean-field method. The SCF calculations were done using a...
From the theoretical viewpoint, much of the phase behaviour of blends containing block copolymers has been anticipated or accounted for. The primary approaches consist of theories based on polymer brushes (in this case block copolymer chains segregated to an interface), Flory-Huggins or random phase approximation mean field theories and the self-consistent mean field theory. The latter has an unsurpassed predictive capability but requires intensive numerical computations, and does not lead itself to intuitive relationships such as scaling laws. [Pg.9]

This name covers all polymer chains (diblocks and others) attached by one end (or end-block) at ( external ) solid/liquid, liquid/air or ( internal ) liquid/liq-uid interfaces [226-228]. Usually this is achieved by the modified chain end, which adsorbs to the surface or is chemically bound to it. Double brushes may be also formed, e.g., by the copolymers A-N, when the joints of two blocks are located at a liquid/liquid interface and each of the blocks is immersed in different liquid. A number of theoretical models have dealt specifically with the case of brush layers immersed in polymer melts (and in solutions of homopolymers). These models include scaling approaches [229, 230], simple Flory-type mean field models [230-233], theories solving self-consistent mean field (SCMF) equations analytically [234,235] or numerically [236-238]. Also first computer simulations have recently been reported for brushes immersed in a melt [239]. [Pg.80]


See other pages where Polymer brushes numerical self-consistent field is mentioned: [Pg.630]    [Pg.102]    [Pg.62]    [Pg.416]    [Pg.10]    [Pg.629]    [Pg.638]    [Pg.264]    [Pg.327]    [Pg.6316]    [Pg.478]    [Pg.479]    [Pg.161]    [Pg.180]    [Pg.85]   


SEARCH



Numerical self-consistent field

Polymer brushes

Polymer field

Self-Consistent Field

Self-consisting fields

© 2024 chempedia.info