Method for separating 1-chloro-3,3,3-trifluoropropene and hydrogen fluoride, and method for producing 1-chloro-3,3,3-trifluoropropene by using same
US-9221732-B2 · Dec 29, 2015 · US
US2018251414A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018251414-A1 |
| Application number | US-201815971364-A |
| Country | US |
| Kind code | A1 |
| Filing date | May 4, 2018 |
| Priority date | Aug 25, 2014 |
| Publication date | Sep 6, 2018 |
| Grant date | — |
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A method for producing a hydrofluoroolefin is provided. The formation of by-products of an over-reduced product having hydrogen added to a material chlorofluoroolefin and an over-reduced product having not only chlorine atoms but also fluorine atoms in the chlorofluoroolefin replaced with hydrogen atoms is suppressed in the method. The method includes reacting a specific chlorofluoroolefin with hydrogen in the presence of a catalyst supported on a carrier to obtain the hydrofluoroolefin. The catalyst is a catalyst composed of an alloy containing at least one platinum group element of palladium and platinum, and at least one second element of copper, gold, lithium, potassium, silver, zinc, tin, lead, and bismuth.
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1 . A method for producing a hydrofluoroolefin, the method comprising: reacting a chlorofluoroolefin of formula (1) with hydrogen in the presence of a catalyst supported on a carrier, to obtain a hydrofluoroolefin of formula (2), wherein the catalyst comprises an alloy containing at least one platinum group element selected from the group consisting of palladium and platinum, and at least one second element selected from the group consisting of copper, gold, potassium, silver, zinc, tin, lead, and bismuth: CZX═CClY (1) wherein X is a fluorine atom or a chlorine atom, Y is a fluorine atom, a chlorine atom or a hydrogen atom, and Z is a fluorine atom or CF 3 ; CZX′═CHY′ (2) wherein X′ is a fluorine atom when X is a fluorine atom, or X′ is a hydrogen atom when X is a chlorine atom, Y′ is a fluorine atom when Y is a fluorine atom, or Y′ is a hydrogen atom when Y is a chlorine atom or a hydrogen atom, and Z is the same as Z in the formula (1). 2 . The method according to claim 1 , wherein the at least one second element is selected from the group consisting of copper, gold, tin, and bismuth. 3 . The method according to claim 1 , wherein a content mass ratio of the at least one platinum group element to the at least one second element in the alloy is from 60:40 to 99:1. 4 . The method according to claim 1 , wherein the catalyst comprises an alloy of palladium and at least one second element selected from the group consisting of copper, gold, tin, and bismuth. 5 . The method according to claim 1 , wherein the carrier is at least one member selected from the group consisting of activated carbon, carbon black, and carbon fibers. 6 . The method according to claim 1 , wherein the carrier is at least one member selected from the group consisting of alumina, silica, titania, and zirconia. 7 . The method according to claim 1 , wherein an amount of the catalyst is from 0.1 to 10 mass % based on the carrier. 8 . The method according to claim 1 , wherein the chlorofluoroolefin and hydrogen are introduced to a catalyst layer packed with the carrier supporting the catalyst, and reacted in a gaseous phase. 9 . The method according to claim 8 , wherein the chlorofluoroolefin and hydrogen are introduced to a gas introduction part of the catalyst layer, and hydrogen is introduced from at least one point between the gas introduction part and a gas discharge part of the catalyst layer. 10 . The method according to claim 8 , wherein said reacting is carried out while a maximum temperature of the catalyst layer is at most 130° C. 11 . The method according to claim 8 , wherein a molar ratio of hydrogen to the chlorofluoroolefin introduced to the catalyst layer [H 2 ]/[Cl] is from 0.1 to 0.7, where [H 2 ] is a total number of moles of hydrogen and [Cl] is number of moles of chlorine atoms in the chlorofluoroolefin. 12 . The method according to claim 1 , wherein the chlorofluoroolefin and hydrogen are reacted in a liquid phase in the presence of the carrier supporting the catalyst. 13 . The method according to claim 1 , wherein the chlorofluoroolefin is at least one member selected from the group consisting of chlorotrifluoroethylene, trans-1,2-dichloro-1,2-difluoroethylene, cis-1,2-dichloro-1,2-difluoroethylene, 1,1-dichloro-2,3,3,3-tetrafluoropropene, and 1-chloro-2,3,3,3-tetrafluoropropene. 14 . The method according to claim 1 , wherein the hydrofluoroolefin is 2,3,3,3-tetrafluoropropene and the chlorofluoroolefin is 1,1-dichloro-2,3,3,3-tetrafluoropropene. 15 . The method according to claim 1 , wherein the at least one second element is selected from the group consisting of gold and bismuth.
with zinc, cadmium or mercury · CPC title
of the platinum group metals · CPC title
with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium · CPC title
of noble metals · CPC title
Copper and noble metals · CPC title
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