Method for producing hydrofluoroolefin
View Patent ↗A hydrofluoroolefin is produced by reacting a chlorofluoroolefin with hydrogen in the presence of a platinum group metal catalyst supported on a carbon carrier to obtain a hydrofluoroolefin. The chlorofluoroolefin is represented by formula (1): CZX═CClY, where X is F or Cl, Y is F, Cl or H, and Z is F or CF 3 . The hydrofluoroolefin is represented by formula (2): CZX′ ═CHY′, where X′ is F when X is F, or X′ is H when X is Cl, Y′ is F when Y is F, or Y′ is H when Y is Cl or H, and Z is the same as Z in the formula (1). The carbon carrier has acidic functional groups, and the total acidic functional group amount in the carbon carrier is at most 50 μmol/g.
1. A method for producing a hydrofluoroolefin, the method comprising:
reacting a chlorofluoroolefin of formula (1) with hydrogen in the presence of a platinum group metal catalyst supported on a carbon carrier, to obtain a hydrofluoroolefin of formula (2):
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),
wherein the carbon carrier has a total acidic functional group amount of at most 50 μmol/g.
2. The method according to claim 1 , wherein the platinum group metal catalyst comprises palladium, a palladium alloy, rhodium or platinum.
3. The method according to claim 1 , wherein the platinum group metal catalyst comprises an alloy of a platinum group element and gold.
4. The method according to claim 3 , wherein the platinum group metal catalyst comprises an alloy of palladium and gold.
5. The method according to claim 1 , wherein the total acidic functional group amount in the carbon carrier is at most 30 μmol/g.
6. The method according to claim 1 , wherein the total acidic functional group amount in the carbon carrier is at most 20 μmol/g.
7. The method according to claim 1 , wherein the carbon carrier has a specific surface area of from 10 to 2,000 m 2 /g.
8. The method according to claim 1 , wherein an amount of the platinum group metal catalyst is from 0.1 to 10 mass % based on the carbon carrier.
9. The method according to claim 8 , wherein the amount of the platinum group metal catalyst is from 0.5 to 1.0 mass % based on the carbon carrier.
10. The method according to claim 1 , wherein the chlorofluoroolefin and hydrogen are introduced to a catalyst layer of a tubular reactor packed with the carbon carrier supporting the catalyst, and reacted in a gaseous phase.
11. The method according to claim 10 , wherein the tubular reactor has a gas introduction part and a gas discharge part, and the chlorofluoroolefin and hydrogen are introduced to the gas introduction part and hydrogen is introduced from at least one point between the gas introduction part and the gas discharge part.
12. The method according to claim 10 , wherein said reacting is carried out while a maximum temperature of the catalyst layer is at most 130° C.
13. The method according to claim 10 , 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 total number of moles of hydrogen and [Cl] is number of moles of chlorine atoms in the chlorofluoroolefin.
14. The method according to claim 1 , wherein the chlorofluoroolefin and hydrogen are reacted in a liquid phase in the presence of the carbon carrier supporting the catalyst.
15. 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.
16. 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.
17. The method according to claim 1 , further comprising:
before said reacting, subjecting the carbon carrier to a heat treatment in an inert gas atmosphere at a temperature of from 350° C. to 1,200° C.
18. The method according to claim 17 , wherein the carbon carrier is subjected to the heat treatment after the platinum group metal catalyst is supported.
19. The method according to claim 17 , wherein the carbon carrier is subjected to the heat treatment before the platinum group metal catalyst is supported.