Article

Aero-Sol−Gel Synthesis of Nanoporous Iron-Oxide Particles:  A Potential Oxidizer for Nanoenergetic Materials

Departments of Mechanical and Chemical Engineering, University of Minnesota, Minneapolis, Minnesota 55455
Chem. Mater., 2004, 16 (8), pp 1466–1471
DOI: 10.1021/cm034740t
Publication Date (Web): March 20, 2004
Copyright © 2004 American Chemical Society

Synopsis

Strategic matching of the time scales of a batch reaction and an aerosol process allows replication of a bulk phase reaction in a micro-droplet. Synthesis of nanoparticles of oxidizer materials with controlled porosity and surface area can be achieved in an aerosol phase reaction.

Abstract

Abstract Image

Interest in developing an oxidizer matrix for reaction with nano-aluminum for energy-intensive applications involving explosives and propellants have led to the development of an aerosol-based sol−gel method (Aero-sol−gel) for preparing nanoporous iron-oxide nanoparticles with high internal surface area. We have employed sol−gel reactions in the aerosol phase using an iron(III) salt with an epoxide in a volatile solvent (ethanol), to generate nanoporous oxidizer nanoparticles. Porosity of the particles results from the nature of the sol−gel chemistry implemented. Energy-dispersive spectrometry (EDS) results indicate that the aerosol-based chemistry is qualitatively similar to that occurring in bulk sol−gel synthesis. The oxidizer particles obtained from the aero-sol−gel experiment are in the 100−250-nm size range as evidenced by SEM and differential mobility analysis (DMA). Porosity of particles is observed qualitatively in the TEM micrographs and quantitatively determined with BET surface area measurements which indicate that these particles have total surface area that is enhanced by a factor of 200 over the geometric surface area. The aero-sol−gel derived iron oxide has also been mixed with nano-aluminum and preliminary ignition tests have been performed to show the effectiveness of the oxidizer particles.

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Article Views: 1,181 Times
Received 8 August 2003
Published online 20 March 2004
Published in print 1 April 2004
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