Structure and Rheology of Cationic Molecular Hydrogels of Quinuclidine Grafted Bile Salts. Influence of the Ionic Strength and Counter-Ion type

被引:32
|
作者
Terech, P. [1 ]
Dourdain, S. [1 ]
Maitra, U. [2 ]
Bhat, S. [2 ]
机构
[1] CEA, INAC, SPrAM, UMR5819,LASSO, F-38054 Grenoble 9, France
[2] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2009年 / 113卷 / 14期
关键词
DEOXYCHOLIC-ACID; LIGHT-SCATTERING; CLOT FORMATIONS; MICELLES; ANALOGS; GELATION; GEL; AGGREGATION; SURFACTANT; ORGANOGELS;
D O I
10.1021/jp809336g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Quinuclidine grafted cationic bile salts are forming salted hydrogels. An extensive investigation of the effect of the electrolyte and counterions on the gelation has been envisaged. The special interest of the quinuclidine grafted bile salt is due to its broader experimental range of gelation to study the effect of electrolyte. Rheological features of the hydrogels are typical of enthalpic networks exhibiting a scaling law of the elastic shear modulus with the concentration (scaling exponent 2.2) modeling cellular solids in which the bending modulus is the dominant parameter. The addition of monovalent salt (NaCl) favors the formation of gels in a first range (0.00117 g cm(-3) (0.02 M)< T-Nacl < 0.04675 g cm(-3) (0.8 M)). At larger salt concentrations, the gels become more heterogeneous with nodal zones in the micron scale. Small-angle neutron scattering experiments have been used to characterize the rigid fibers (R approximate to 68 angstrom) and the nodal zones. Stress sweep and creep-recovery measurements are used to relate the lack of linear viscoelastic domain to a mechanism of disentanglement of the fibers from their associations into fagots. The electrostatic interactions can be screened by addition of salt to induce a progressive evolution toward flocculation. SEM, UV absorbance, and SAXS study of the Bragg peak at large Q-values complete the investigation.
引用
收藏
页码:4619 / 4630
页数:12
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