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Supramolecular assembly of gelatin and inorganic polyanions: Fine-tuning the mechanical properties of nanocomposites by varying their composition and microstructure

Article dans une revue avec comité de lecture
Author
BAROUDI, Imane
14457 Institut Lavoisier de Versailles [ILV]
SIMONNET-JÉGAT, Corine
14457 Institut Lavoisier de Versailles [ILV]
ROCH-MARCHAL, Catherine
14457 Institut Lavoisier de Versailles [ILV]
LECLERC-LARONZE, Nathalie
14457 Institut Lavoisier de Versailles [ILV]
LIVAGE, Carine
14457 Institut Lavoisier de Versailles [ILV]
MARTINEAU, Charlotte
14457 Institut Lavoisier de Versailles [ILV]
GERVAIS, Christel
1118 Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) [LCMCP (site Paris VI)]
CADOT, Emmanuel
14457 Institut Lavoisier de Versailles [ILV]
CARN, Florent
170 Matière et Systèmes Complexes [MSC]
FAYOLLE, Bruno
86289 Laboratoire Procédés et Ingénierie en Mécanique et Matériaux [PIMM]
STEUNOU, Nathalie
1118 Laboratoire de Chimie de la Matière Condensée de Paris (site Paris VI) [LCMCP (site Paris VI)]
14457 Institut Lavoisier de Versailles [ILV]

URI
http://hdl.handle.net/10985/9992
DOI
10.1021/cm502605q
Date
2015
Journal
Chemistry of Materials

Abstract

A series of bionanocomposites has been synthesized through a complex coacervation process inducing the assembly of gelatin with a wide range of inorganic polyanions (IPyAs) differing by their diameter and charge and including polyoxometalates (POMs) and a polythiomolybdate cluster. The microstructure and stoichiometry of these hybrid coacervates, which are strongly dependent on the charge matching between both components, have been studied by combining Fourier transform infrared (FT-IR) spectroscopy, solid-state nuclear magnetic resonance (NMR), thermogravimetric analysis (TGA), elemental analysis, differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and energy-dispersive X-ray (EDX) elemental mapping. The mechanical properties of these materials were deeply characterized by tensile measurements at large deformation, revealing different behaviors (i.e., elastomer and ductile), depending on the nature of the IPyA. It is noteworthy that the mechanical properties of these bionanocomposites are strongly enhanced, compared to pure gelatin hydrogels. When attempting to connect structure and properties in these bionanocomposites, we have demonstrated that the density of cross-links (gelatin triple helices and IPyA) is the key parameter to control the extensibility of these materials;

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