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Experimental study of atmospheric pressure chemical vapor deposition of silicon carbide from methyltrichlorosilane

Published online by Cambridge University Press:  31 January 2011

George D. Papasouliotis
Affiliation:
Department of Chemical Engineering, University of Rochester, Rochester, New York 14627
Stratis V. Sotirchos*
Affiliation:
Department of Chemical Engineering, University of Rochester, Rochester, New York 14627 and Institute of Chemical Engineering and High Temperature Chemical Processes, P.O. Box 1414, 26500 Patras, GREECE
*
b) Address all correspondence to this author.
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Abstract

A comprehensive study of the chemical vapor deposition of SiC from methyltrichlorosilane at atmospheric pressure was conducted in this study; its main objectives were to identify the range of operating parameters in which stoichiometric SiC could be deposited and the generation of reliable kinetic data that could be used for the design of atmospheric pressure processes of chemical vapor deposition or chemical vapor infiltration of SiC. Deposition experiments were conducted in a hot-wall, cylindrical reactor at temperature ranging from 1273 to 573 K on flat graphite substrates or thin molybdenum wires aligned with the axis of the reactor. The obtained results showed that the deposition rate and the deposit stoichiometry varied markedly with the distance from the entrance of the reactor. The deposition rate exhibited, depending on the reaction temperature, one or two pronounced maxima before the beginning of the isothermal zone of the reaction, whereas the deposit stoichiometry showed an abrupt transition from almost silicon to stoichiometric silicon carbide after the first maximum. Experiments with HCl added in the feed showed that the presence of HCl could cause complete suppression of the deposition of silicon and lead to smoother variation of the SiC deposition rate with the residence time in the reactor. It is believed that this effect could be exploited to improve the uniformity of SiC deposition in chemical vapor deposition reactors or in the interior of porous preforms.

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Articles
Copyright
Copyright © Materials Research Society 1999

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