Effect of concentration regime on rheological properties of sodium polymethacrylate and its complexes with polystyrene-poly(N-ethyl-4- vinylpyridinium bromide) block copolymer in aqueous salt solutionстатья
Информация о цитировании статьи получена из
Web of Science ,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 18 июля 2013 г.
Авторы:
Litmanovich E.A.a ,
Syaduk G.V.a ,
Lysenko E.A.a ,
Zezin A.B.a ,
Kabanov A.V.b ,
Kabanov V.A.c
Журнал:
Polymer Science, Series A
Том:
48
Номер:
9
Год издания:
2006
Издательство:
Pleiades Publishing, Ltd
Местоположение издательства:
Road Town, United Kingdom
Первая страница:
997
Последняя страница:
1003
DOI:
10.1134/S0965545X06090161
Аннотация:
The effect of concentration on the behavior of high-molecular-mass sodium polymethacrylate (M w = 3.9 × 105) in a 0.1 M NaCl aqueous solution was studied by the methods of dynamic and static light scattering, and capillary and rotational viscometry. It was shown that the concentration corresponding to the formation of fluctuation network of polyelectrolyte entanglements (6.4%) is substantially higher than the crossover concentration (0.25%). This fact indicates the existence of a wide concentration interval for a semidilute unentangled polyanion solution. The introduction of minor amounts of micelles of cationic amphiphilic polystyrene-poly(N-ethyl-4- vinylpyridinium bromide) diblock copolymer is accompanied by the development of the network of an interpolyelectrolyte complex. The junctions of this network are diblock copolymer micelles that are linked to polyanion macromolecules via salt bonds. The formation of interpolyelectrolyte network leads to the additional structuring of the sodium polymethacrylate solution and an increase in its viscosity. The growth in viscosity is most pronounced in the concentration region above the concentration corresponding to the formation of entanglement network of the free polyanion. © Nauka/Interperiodica 2006.
Добавил в систему:
Зезин Александр Борисович