posted on 2016-06-09, 12:24authored byKenneth N. Marsh, Tony K. Morris, G. P. Peterson, Thomas J. Hughes, Quentin Ran, James C. Holste
The method for the
preparation of elemental silicon of sufficient
purity for the fabrication of electronic devices is by first converting
silicon oxide to silicon–hydrogen-chloride compounds, purifying
the material as a fluid mixture, and then converting the product to
solid silicon. During the purification process a mixture of dichlorosilane
(SiH2Cl2), trichlorosilane (SiHCl3), and tetrachlorosilane or silicon tetrachloride (SiCl4) are formed with each of the components in significant quantities.
Models that describe the vapor–liquid equilibrium behavior
for the mixtures are required to design appropriate separation and
purification processes. Pure fluid properties form the starting point
for most mixture models, hence the importance of vapor pressures for
the pure materials. In this work we report measurements of the vapor
pressures for three of the most important fluids in the silicon production
process, dichlorosilane, trichlorosilane, and tetrachlorosilane. Our
results are compared with measurements reported previously. The instability
of chlorosilanes complicates the experimental procedures because of
the corrosive nature of the products formed, and in particular the
potential for self-ignition upon exposure to moist air. The experimental
procedures used to minimize the hazards and to avoid contamination
of the fluids are described.