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Please use this identifier to cite or link to this item: http://apo.ansto.gov.au/dspace/handle/10238/3081

Title: Synthesis of nanoporous silicon carbide via the preceramic polymer route.
Authors: Maddocks, AR
Cassidy, DJ
Jones, AS
Harris, AT
Keywords: Porous Materials
Carbides
X-Ray Diffraction
Adsorption
Silicon Carbides
Polymers
Issue Date: 15-Feb-2009
Publisher: Elsevier
Citation: Maddocks, A. R., Cassidy, D. J., Jones, A. S., & Harris, A. T. (2009). Synthesis of nanoporous silicon carbide via the preceramic polymer route. Materials Chemistry and Physics, 113(2-3), 861-867.
Abstract: Nanoporous silicon carbide materials were prepared by the pyrolysis of the preceramic polymer, polycarbosilane (PCS), with and without the addition of an inert filler (nano- and micron-sized silicon carbide powders). Hydrosilylation crosslinking of PCS with divinylbenzene prior to pyrolysis appeared to have little influence on the development of micro- and mesoporosity. Maximum micropore volumes were 0.28 cm3 g−1 for non-crosslinked PCS and 0.25, 0.33 and 0.32 cm3 g−1 for PCS crosslinked with 2, 6 and 10 wt.% DVB respectively. Micropore volumes decreased under hydrothermal conditions to 0.03 cm3 g−1 for non-crosslinked and 0 cm3 g−1 for crosslinked PCS. Porosity was also lost at temperatures above 700°C. The addition of nano-sized SiC powders to PCS prior to pyrolysis maintained mesoporosity to temperatures of 1200°C, however, micron-sized SiC powders did not maintain porosity above 800°C. The modal pore size in pellets formed by compressing micron-sized powders with the preceramic polymer was 5 μm compared to 30 nm when nano-sized powders were used. © 2009, Elsevier Ltd.
URI: http://dx.doi.org/10.1016/j.matchemphys.2008.08.064
http://apo.ansto.gov.au/dspace/handle/10238/3081
ISSN: 0254-0584
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