Casimir force in critical ternary polymer solutions

Consider a mixture of two incompatible polymers A and B in a common good solvent, confined between two parallel plates separated by a finite distance L. We assume that these plates strongly attract one of the two polymers close to the consolute point (critical adsorption). The plates then experien...

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Збережено в:
Бібліографічні деталі
Видавець:Інститут фізики конденсованих систем НАН України
Дата:2004
Автори: Ridouane, H., Hachem, E.-K., Benhamou, M.
Формат: Стаття
Мова:English
Опубліковано: Інститут фізики конденсованих систем НАН України 2004
Назва видання:Condensed Matter Physics
Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/118888
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Цитувати:Casimir force in critical ternary polymer solutions / H. Ridouane, E.-K. Hachem, M. Benhamou // Condensed Matter Physics. — 2004. — Т. 7, № 1(37). — С. 63-78. — Бібліогр.: 59 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Резюме:Consider a mixture of two incompatible polymers A and B in a common good solvent, confined between two parallel plates separated by a finite distance L. We assume that these plates strongly attract one of the two polymers close to the consolute point (critical adsorption). The plates then experience an effective force resulting from strong fluctuations of the composition. To simplify, we suppose that either plates have the same preference to attract one component (symmetric plates) or they have an opposed preference (asymmetric plates). The force is attractive for symmetric plates and repulsive for asymmetric ones. We first exactly compute the force using the blob model, and find that the attractive and repulsive forces decay similarly to L⁻⁴. To go beyond the blob model that is a mean-field theory, and in order to get a correct induced force, we apply the Renormalization-Group to a φ⁴ -field theory ( φ is the composition fluctuation), with two suitable boundary conditions at the surfaces. The main result is that the expected force is the sum of two contributions. The first one is the mean-field contribution decaying as L⁻⁴, and the second one is the force deviation originating from strong fluctuations of the composition that decreases rather as L⁻³. This implies the existence of some cross-over distance L* ∼ aNφ¹/² ( a is the monomer size, N is the polymerization degree of chains and φ is the monomer volumic fraction), which separates two distance-regimes. For small distances (L < L*) , the mean-field force dominates, while for high distances (L > L*) the fluctuation force is more important.