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In-situ generation <strong>of</strong> silica <strong>in</strong> epoxy matrix and modified epoxy matrix via solgel<br />

process<br />

K.K.Iynesh Kumar and B.Kothandaraman<br />

Department <strong>of</strong> Rubber and Plastics technology, Madras Institute <strong>of</strong> Technology, Anna University,<br />

Chennai, India.<br />

Email: iyneshkumar@gmail.com bkraman@mit<strong>in</strong>dia.edu<br />

ABSTRACT<br />

The precipitation <strong>of</strong> nanosilica was done through Sol-Gel process with Tetraethoxysilane (TEOS)<br />

as silica precursor at room temperature. The choice <strong>of</strong> epoxy as a matrix was made because <strong>of</strong> its polar<br />

nature which can <strong>in</strong>teract with <strong>in</strong>-situ generated silica. The am<strong>in</strong>e conta<strong>in</strong><strong>in</strong>g polydimethylsiloxane<br />

(PDMS) was used as liquid rubber modifier.<br />

The precipitation was done directly on the organic matrix <strong>in</strong> the presence <strong>of</strong> Water,<br />

Tetraethoxysilane (TEOS) and Ethanol as mutual solvent. The nanocomposite was cured by triethylene<br />

tetram<strong>in</strong>e at room temperature. To enhance bond<strong>in</strong>g between organic and <strong>in</strong>organic matrix<br />

Dichlorodimethylsilane (DDS) was used as a coupl<strong>in</strong>g agent.<br />

Dispersion <strong>of</strong> silica particles was observed through Atomic force microscope (AFM). Infrared<br />

spectroscopic studies <strong>in</strong>dicated the occurrence <strong>of</strong> chemical <strong>in</strong>teraction with<strong>in</strong> the epoxy/silica under<br />

ambient conditions. The glass transition temperature (Tg) was <strong>in</strong>vestigated through Differential scann<strong>in</strong>g<br />

calorimeter (DSC). The thermal stability and filler content <strong>of</strong> the material were predicted through<br />

Thermogravimetricanalyser (TGA). The mechanical re<strong>in</strong>forcement with<strong>in</strong> the material was demonstrated<br />

through flexural behavior <strong>of</strong> the material.<br />

INTRODUCTION<br />

The sol-gel process, which is ma<strong>in</strong>ly based on <strong>in</strong>organic polymerization reactions, is a<br />

chemical synthesis method <strong>in</strong>itially used for the preparation <strong>of</strong> <strong>in</strong>organic materials such as glasses and<br />

ceramics. Its unique low-temperature process<strong>in</strong>g characteristic also provides unique opportunities to make<br />

pure and well-controlled composition organic/<strong>in</strong>organic hybrid materials through the <strong>in</strong>corporation <strong>of</strong> low<br />

molecular weight and oligomeric/polymeric organic molecules with appropriate <strong>in</strong>organic moieties at<br />

temperatures under which the organics can survive. The organic/<strong>in</strong>organic hybrid materials made <strong>in</strong> this<br />

way, which have been termed “creamers” by Wilkes [1] and “ormosils” or” ormocers” by Schmidt[2].,<br />

are normally nanocomposites and have the potential for provid<strong>in</strong>g unique comb<strong>in</strong>ations <strong>of</strong> properties<br />

which cannot be atta<strong>in</strong>ed by other materials .<br />

For the past decade, organic/<strong>in</strong>organic nanocomposites prepared by the sol-gel process<br />

have attracted a great deal <strong>of</strong> attention, especially <strong>in</strong> the fields <strong>of</strong> ceramics, polymer chemistry, organic<br />

and <strong>in</strong>organic chemistry, and physics. The preparation, characterization, and applications <strong>of</strong><br />

organic/<strong>in</strong>organic hybrid materials have become a fast expand<strong>in</strong>g area <strong>of</strong> research <strong>in</strong> material science. The<br />

major driv<strong>in</strong>g forces beh<strong>in</strong>d the <strong>in</strong>tense activities <strong>in</strong> this area are the new and different properties <strong>of</strong> the<br />

nanocomposites which the traditional macroscale composites and conventional materials don’t have. For<br />

example, unlike the traditional composite materials which have macroscale doma<strong>in</strong> size <strong>of</strong> millimeter and<br />

even micrometer scale, most <strong>of</strong> the organic/<strong>in</strong>organic hybrid materials are nanoscopic, with the physical

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