Fluorinated cycloalkene functionalized silicas
US-2016280725-A1 · Sep 29, 2016 · US
US2022401907A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022401907-A1 |
| Application number | US-202017765825-A |
| Country | US |
| Kind code | A1 |
| Filing date | Sep 30, 2020 |
| Priority date | Oct 1, 2019 |
| Publication date | Dec 22, 2022 |
| Grant date | — |
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Described herein are thermal condensation reactors and processes of using the same. A presently described thermal condensation reactor includes a heat transfer chamber, wherein the heat transfer chamber is a fluidized bed having a fluidization gas flow in a first direction, and wherein the heat transfer chamber has a plurality of heating zones that may be maintained at different temperatures, and a plurality of reaction tubes disposed in the heat transfer chamber in a second direction perpendicular to the fluidization gas flow, each reaction tube having a reactant gas flow that passes through the plurality of heating zones.
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1 . A thermal condensation reactor, comprising: a heat transfer chamber, wherein the heat transfer chamber is a fluidized bed having a fluidization gas flow in a first direction, and wherein the heat transfer chamber comprises a plurality of heating zones that are maintained at different temperatures; and a plurality of reaction tubes disposed in the heat transfer chamber in a second direction that is perpendicular to the fluidization gas flow, each of the plurality of reaction tubes having a reactant gas flow that passes through the plurality of heating zones. 2 . The thermal condensation reactor of claim 1 , wherein the fluidization gas flow is vertical and the reactant gas flow is horizontal. 3 . The thermal condensation reactor of claim 1 , further comprising a port for introducing a shroud gas, wherein the shroud gas flows through a portion of each of the plurality of reaction tubes. 4 . The thermal condensation reactor of claim 3 , wherein the reactant gas is a mixture of vinyl chloride and trichlorosilane, and wherein the shroud gas is silicon tetrachloride. 5 . The thermal condensation reactor of claim 1 , wherein each of the plurality of reaction tubes is associated with a sealing gland integrated with an interior liner comprising either graphite, carbon fiber carbon composite, silicon carbide-coated isomolded graphite, or silicon carbide. 6 . The thermal condensation reactor of claim 1 , further comprising a bonnet for covering the gas flow inlets of the plurality of reaction tubes. 7 . The thermal condensation reactor of claim 1 , further comprising a floating head for covering the gas flow outlets of the plurality of reaction tubes, wherein the floating head is moveable in the second direction. 8 . The thermal condensation reactor of claim 7 , further comprising a cooling transition unit that encompasses the floating head, and wherein the cooling transition unit is also a fluidized bed. 9 . The thermal condensation reactor of claim 1 , further comprising one or more roller supports associated with the heat transfer chamber to accommodate thermal expansion. 10 . The thermal condensation reactor of claim 1 , further comprising one or more baffles disposed in the heat transfer chamber. 11 . A process for producing an alkenyl-functional halosilane comprising: premixing an alkenyl halide and a hydrido-functional halosilane to create a reactant gas; introducing the reactant gas into a plurality of reaction tubes arranged horizontally in a fluidized bed; and passing the reactant gas through a plurality of heating zones in the fluidized bed, wherein the plurality of heating zones are maintained at different temperatures. 12 . The process of claim 11 , further comprising diluting the reactant gas with a shroud gas comprising of the halogenation product of the hydrido-functional halosilane and hydrogen halide. 13 . The process of claim 11 , wherein the alkenyl halide is vinyl chloride. 14 . The process of claim 11 , wherein the hydrido-functional halosilane has formula R w H x SiX (4−w−x) , where subscript w is 0 to 2, subscript x is 1 to 3, and a quantity (w+x) is 1 to 3; each R is an independently selected monovalent hydrocarbon group of 1 to 18 carbon atoms that is free of aliphatic unsaturation, and each X is an independently selected halogen atom. 15 . The process of claim 14 , wherein the hydrido-functional halosilane is trichlorosilane. 16 . The process of claim 12 , wherein the alkenyl halide is vinyl chloride. 17 . The process of claim 12 , wherein the hydrido-functional halosilane has formula R w H x SiX (4−w−x) , where subscript w is 0 to 2, subscript x is 1 to 3, and a quantity (w+x) is 1 to 3; each R is an independently selected monovalent hydrocarbon group of 1 to 18 carbon atoms that is free of aliphatic unsaturation, and each X is an independently selected halogen atom. 18 . The process of claim 13 , wherein the hydrido-functional halosilane has formula R w H x SiX (4−w−x) , where subscript w is 0 to 2, subscript x is 1 to 3, and a quantity (w+x) is 1 to 3; each R is an independently selected monovalent hydrocarbon group of 1 to 18 carbon atoms that is free of aliphatic unsaturation, and each X is an independently selected halogen atom. 19 . The process of claim 16 , wherein the hydrido-functional halosilane has formula R w H x SiX (4−w−x) , where subscript w is 0 to 2, subscript x is 1 to 3, and a quantity (w+x) is 1 to 3; each R is an independently selected monovalent hydrocarbon group of 1 to 18 carbon atoms that is free of aliphatic unsaturation, and each X is an independently selected halogen atom.
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