Isooctane production from field butane
US-12252466-B2 · Mar 18, 2025 · US
US12415175B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12415175-B2 |
| Application number | US-202117995320-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 24, 2021 |
| Priority date | May 8, 2020 |
| Publication date | Sep 16, 2025 |
| Grant date | Sep 16, 2025 |
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Catalysts for the hydrogenolysis of butane are described. A supported catalyst for hydrogenolysis of butane to ethane can include a support and a catalytic crystalline bimetallic composition that can include a molybdenum-iridium (Mo—Ir) crystalline composition attached to the support. The supported catalyst has a BET specific surface area of at least 100 m2/g, preferably 100 m2/g to 500 m2/g. Method of use and methods of making the catalyst are also described.
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The invention claimed is: 1. A supported butane hydrogenolysis catalyst for hydrogenolysis of butane to ethane, the supported catalyst comprising: a support; and a crystalline catalytic bimetallic material comprising a crystalline catalytic molybdenum—iridium (Mo—Ir) composition attached to the support, wherein the supported catalyst has a Brunauer-Emmett-Teller (BET) surface area of 100 m 2 /g to 150 m 2 /g, wherein the supported catalyst has a butane conversion of at least 50%; and wherein the support comprises alumina, wherein the alumina is gamma-alumina. 2. The supported butane hydrogenolysis catalyst of claim 1 , wherein the support comprises a member selected from the group consisting of zeolite, titania (TiO 2 ) and silica (SiO 2 ), or a combination thereof. 3. The supported butane hydrogenolysis catalyst of claim 2 , wherein the BET surface area is 100 m 2 /g. 4. The supported butane hydrogenolysis catalyst of claim 1 , wherein the support comprises a zeolite. 5. The supported butane hydrogenolysis catalyst of claim 4 , wherein the supported butane hydrogenolysis catalyst has a BET surface area of 150 m 2 /g. 6. The supported butane hydrogenolysis catalyst of claim 4 , wherein the supported butane hydrogenolysis catalyst has a BET surface area of 100 m 2 /g. 7. The supported butane hydrogenolysis catalyst of claim 1 , wherein the Mo—Ir composition has a molar ratio of Mo:Ir of 1:3 to 4:1. 8. The supported butane hydrogenolysis catalyst of claim 1 , wherein the crystalline catalytic Mo—Ir composition comprises a MoIr 3 crystalline structure, a Mo 3 Ir crystalline structure, or a MoIr 4 crystalline structure, or a mixture thereof. 9. The supported butane hydrogenolysis catalyst of claim 8 , comprising 0.1 wt. % to 5 wt. % of the Mo—Ir composition having the MoIr 3 crystalline structure. 10. The supported butane hydrogenolysis catalyst of claim 9 , comprising 0.4 wt. % to 0.8 wt. % of MoIr 3 on a Al 2 O 3 support. 11. The supported butane hydrogenolysis catalyst of claim 10 , wherein the supported butane hydrogenolysis catalyst is a 0.6 wt. % MoIr 3 on the Al 2 O 3 support catalyst. 12. The supported butane hydrogenolysis catalyst of claim 1 , wherein the supported butane hydrogenolysis catalyst has a BET surface area of 100 m 2 /g. 13. A method to produce ethane, the method comprising contacting the supported butane hydrogenolysis catalyst of claim 1 with butane under conditions sufficient for hydrogenolysis of butane and produce ethane wherein the contacting conditions comprise a temperature of 240° C. to 325° C., a pressure of 0.35 MPa to 1.4 MPa, a butane weighted hourly velocity of 1 to 10 hr −1 , or any combination thereof. 14. The method of claim 13 , wherein the conditions comprise a temperature of 260° C. to 300° C. 15. The method of claim 13 , wherein the supported butane hydrogenolysis catalyst has a BET surface area of 100 m 2 /g. 16. The method of claim 13 , wherein the supported butane hydrogenolysis catalyst has a BET surface area of 150 m 2 /g. 17. The method of claim 13 , wherein the butane comprises n-butane, iso-butane, or a mixture thereof. 18. A method of producing the supported butane hydrogenolysis catalyst of claim 1 , the method comprising: impregnating a support comprising gamma-alumina with a catalytic Mo/Ir precursor composition to form an impregnated support/Mo—Ir precursor composition material; drying the impregnated support/Mo—Ir precursor composition material to form a dried impregnated support/Mo—Ir precursor composition material; and calcining the dried impregnated support/Mo—Ir precursor composition material at a temperature of 85° C. to 100° C. for 2 to 24 hours to form the supported butane hydrogenolysis catalyst; wherein impregnating comprises adding the catalytic Mo/Ir precursor composition dropwise onto the support and agitating the impregnated support/catalytic Mo/Ir precursor composition for 2 to 24 hours; and heat-treating. 19. The method of claim 18 , wherein the support comprises a member selected from the group consisting of gamma-alumina extrudates, a zeolite, titania extrudates, silica extrudates, or a mixture thereof. 20. A supported butane hydrogenolysis catalyst produced by the method of claim 18 .
100-500 m2/g · CPC title
10-100 m2/g · CPC title
Chromium, molybdenum or tungsten · CPC title
Alumina · CPC title
from acyclic hydrocarbons · CPC title
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