Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Silane | HCID 23953 | — |
| Reactant | 1,1,1-Trichloro-2,2,2-trimethyldisilane | HCID 87413 | — |
| Reactant | Dichlorotetramethyldisilane | HCID 170204 | — |
| Reactant | Tetrachlorodimethyldisilane | HCID 13908101 | — |
| Product | Silane | HCID 23953 | — |
| Product | Trichlorosilane | HCID 24811 | 20% |
| Product | Silicon tetrachloride | HCID 24816 | 40% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344578B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-3c7586032bbc48af9bded03705255f79 |
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| Source note | uspto-grants-2002_02 |
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