The structure–property relationship in LAPONITE® materials: from Wigner glasses to strong self-healing hydrogels formed by non-covalent interactions. Issue 6 (22nd November 2018)

• Record Type: Journal Article
• Authors: Becher, Tiago B.; Braga, Carolyne B.; Bertuzzi, Diego L.; Ramos, Miguel D.; Hassan, Ayaz; Crespilho, Frank N.; Ornelas, Catia
• Is Part Of: Soft matter. Volume 15:Issue 6(2019)
• Page Start: 1278
• Page End: 1289
• Publication Date: 2018-11-22
• Subjects: Soft condensed matter -- Periodicals; 530.413
• DOI: 10.1039/c8sm01965g
• Languages: English
• ISSNs: 1744-683X

Abstract

Abstract : Rheology, SAXS, and dynamic light scattering (DLS) analysis, zeta potential measurement, scanning electron microscopy (SEM), and micro-FTIR and absorbance spectroscopy were used to enlighten the controversial literature about LAPONITE® materials. Abstract : Rheology, small-angle X-ray scattering (SAXS), and dynamic light scattering (DLS) analysis, zeta potential measurement, scanning electron microscopy (SEM), and micro-FTIR and absorbance spectroscopy were used to enlighten the controversial literature about LAPONITE® materials. Our data suggest that pristine LAPONITE® in water does not form hydrogels induced by the so-called "house of cards" assembly, but rather forms Wigner glasses governed by repulsive forces. Ionic interactions between anisotropic LAPONITE® nanodiscs, sodium polyacrylate and inorganic salts afforded hydrogels that were transparent, self-standing, moldable, strong, and biocompatible with shear-thinning and self-healing behavior. An extensive study on the role of salts in the gelification process dictates a trend that relates the valence of cations with the viscoelastic properties of the bulk material ( G ′ values follow the trend, monovalent < divalent < trivalent). These hydrogels present G ′ values up to 5.1 × 10 4 Pa, which are considered high values for non-covalent hydrogels. Hydrogels crosslinked with sodium phosphate salts are biocompatible, and might be valid candidates for injectable drug delivery systems due to their shear-thinning behavior with rapid self-healing after injection.