Hydrochloric Acid → Silicon tetrachloride
Reaction equation
[SiH4].Cl.[Cl:3][Si:4]([Cl:10])([Cl:9])[Si](Cl)(C)C.[Cl:11][Si:12]([Cl:18])([Cl:17])[Si](C)(C)C.[Cl:19][Si](Cl)(C)[Si](C)(C)C>>[SiH4:4].[Cl:11][SiH:12]([Cl:18])[Cl:17].[Si:4]([Cl:10])([Cl:19])([Cl:9])[Cl:3]Participants
Procedure
70 ml/h of high-boiling residue from the silane synthesis having a boiling point of greater than 150° C. and 25 I/h of gaseous hydrogen chloride were fed concurrently at room temperature and ambient pressure into an electrically heated laboratory fluidized-bed reactor having a length of 500 mm and an internal diameter of 40 mm, filled with 266 g of silicon, d(0.5): 70-80 μm. The temperature was set to 600° C. The high-boiling residue comprised 75 % of disilanes, a mixture of tetrachlorodimethyldisilane, trichlorotrimethyldisilane, dichlorotetramethyldisilane and other silanes. A more precise assignment was difficult because of the large number of by-products. After 20 hours of operation, the experiment was stopped without deposits having been formed. About 100 g/h of silane mixture comprising, as main constituents, about 20 % of trichlorosilane and about 40% of silicon tetrachloride was formed. After separation of the trichlorosilane and silicon tetrachloride, a silane cleavage product having the composition set forth in Table 1 was obtained during the experiment.
Workup
- customwere fed concurrently at room temperature
- additionan internal diameter of 40 mm, filled with 266 g of silicon, d(0.5)
- customwas set to 600° C
- customhaving been formed
Sources & evidence
- ORD record
- ord-3c7586032bbc48af9bded03705255f79
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06344578B1
Reaction notes
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