Process for producing hydrofluoroolefin

Patent metadata

Field	Value
Publication number	US-10781151-B2
Application number	US-201815971364-A
Country	US
Kind code	B2
Filing date	May 4, 2018
Priority date	Aug 25, 2014
Publication date	Sep 22, 2020
Grant date	Sep 22, 2020

Abstract

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.

First claim

What is claimed is:

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):
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 CF3;
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 (I);
wherein
the chlorofluoroolefin of formula (I) does not comprise chlorotrifluoroethylene;
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, potassium, silver, zinc, tin, lead, and bismuth;
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, and
the reacting is carried out while a maximum temperature of the catalyst supported on the carrier is controlled to be at most 130° C.

2. The method according to claim 1 , wherein the at least one second element is selected from the group consisting of copper, tin, and bismuth.

3. 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, tin, and bismuth.

4. 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.

5. 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.

6. The method according to claim 1 , wherein an amount of the catalyst is from 0.1 to 10 mass % based on the carrier.

7. 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.

8. The method according to claim 7 , 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.

9. The method according to claim 7 , wherein said reacting is carried out while a maximum temperature of the catalyst layer is at most 130 C.

10. The method according to claim 7 , wherein a molar ratio of hydrogen to the chlorofluoroolefin introduced to the catalyst layer [H2]/[Cl] is from 0.1 to 0.7, where [H2] is a total number of moles of hydrogen and [C1] is a number of moles of chlorine atoms in the chlorofluoroolefin.

11. 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.

12. The method according to claim 1 , wherein the chlorofluoroolefin is at least one member selected from the group consisting of trans-1,2-dichloro-1,2-difluoroethylene, cis-1,2-dichloro-1,2-difluoroethylene, 1-dichloro-2,3,3,3-tetrafluoropropene, and 1-chloro-2,3,3,3-tetrafluoropropene.

13. 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.

14. The method according to claim 1 , wherein the at least one second element is bismuth.

Assignees

• Agc Inc

Inventors

• Terazono Shinji
• Wang Xu
• Kanda Masahiro
• Kawaguchi Satoshi
• Kasagawa Mitsugu

Classifications

• C07B61/00

  Other general methods · CPC title

• B01J23/6447

  Bismuth · CPC title

• B01J23/60

  with zinc, cadmium or mercury · CPC title

• B01J23/8926

  Copper and noble metals · CPC title

• B01J23/64

  with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium · CPC title