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Structural Regime Identification in Ionotropic Alginate Gels: Influence of the Cation Nature and Alginate Structure
Author(s) -
Pierre Agulhon,
Mike Robitzer,
Laurent David,
Françoise Quignard
Publication year - 2011
Publication title -
biomacromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.689
H-Index - 220
eISSN - 1526-4602
pISSN - 1525-7797
DOI - 10.1021/bm201477g
Subject(s) - small angle x ray scattering , supercritical drying , self healing hydrogels , ionotropic effect , chemical engineering , morphology (biology) , chemistry , aerogel , nanostructure , biopolymer , polymer chemistry , scattering , organic chemistry , polymer , nmda receptor , physics , receptor , biochemistry , biology , optics , genetics , engineering
The morphologies of several ionotropic alginate hydrogels and aerogels were investigated by SAXS according to the nature of the divalent metal cation (Mn(2+), Co(2+), Zn(2+), Cu(2+)) and the guluronic fraction of the alginate. All alginate hydrogel and aerogel samples show isotropic small-angle X-ray scattering. Gelation results from cooperative associations of cations and chain segments and yields different nanostructures, that is, nanofibrillar morphology or multiple junction morphology, according to cation type and eventually mannuronic/guluronic ratio. Therefore, Mn and Cu gels present the same morphology whatever the guluronic ratio, whereas Co and Zn gels yield different nanostructures. In the size range investigated by SAXS (~10-200 Å), the structure of aerogels obtained by CO(2) supercritical drying is found to be inherited from the morphology of the parent hydrogel whatever the initial structural regime.

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