J. Am. Chem. Soc., 129 (1), 98 -108, 2007. 10.1021/ja0653167 S0002-7863(06)05316-9
Web Release Date: December 15, 2006

Copyright © 2006 American Chemical Society

Composite Particles of Polyethylene @ Silica

Hanan Sertchook, Hila Elimelech, Carina Makarov, Rafail Khalfin, Yachin Cohen, Michael Shuster, Florence Babonneau, and David Avnir*

Contribution from the Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel, Faculty of Chemical Engineering, Technion-Israel Institute of Technology, Haifa 32000, Israel, Carmel Olefins Ltd., P.O.B. 1468, Haifa 31014, Israel, and Chimie de la Matiere Condensee, Universite Paris 6 - T54-E5, 4 Place Jussieu, 75252 Paris Cedex 05, France

david@chem.ch.huji.ac.il

Received July 25, 2006

Abstract:

Polyethylene (PE) and silica are perhaps the simplest and most common organic and inorganic polymers, respectively. We describe, for the first time, a physically interpenetrating nanocomposite between these two elementary polymers. While polymer-silica composites are well known, the nanometric physical blending of PE and silica has remained a challenge. A method for the preparation of such materials, which is based on the entrapment of dissolved PE in a polymerizing tetraethoxysilane (TEOS) system, has been developed. Specifically, the preparation of submicron particles of low-density PE@silica and high-density PE@silica is detailed, which is based on carrying out a silica sol-gel polycondensation process within emulsion droplets of TEOS dissolved PE, at elevated temperatures. The key to the successful preparation of this new composite has been the identification of a surfactant, PE-b-PEG, that is capable of stabilizing the emulsion and promoting the dissolution of the PE. A mechanism for the formation of the particles as well as their inner structure are proposed, based on a large battery of analyses, including transmission electron microscopy (TEM) and scanning electron microscopies (SEM), surface area and porosity analyses, various thermal analyses including thermal gravimetric analysis (TGA/DTA) and differential scanning calorimetry (DSC) measurements, small-angle X-ray scattering (SAXS) measurements and solid-state NMR spectroscopy.


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