Bimetallic catalysts supported on zeolites for selective conversion of n-butane to ethane

Patent metadata

Field	Value
Publication number	US-11559795-B2
Application number	US-201917262288-A
Country	US
Kind code	B2
Filing date	Sep 17, 2019
Priority date	Sep 19, 2018
Publication date	Jan 24, 2023
Grant date	Jan 24, 2023

Abstract

A hydrogenolysis bimetallic supported catalyst comprising a first metal, a second metal, and a zeolitic support; wherein the first metal and the second metal are different; and wherein the first metal and the second metal can each independently be selected from the group consisting of iridium (Ir), platinum (Pt), rhodium (Rh), ruthenium (Ru), palladium (Pd), molybdenum (Mo), tungsten (W), nickel (Ni), and cobalt (Co).

First claim

What is claimed is:

1. A hydrogenolysis bimetallic supported catalyst comprising a first metal, a second metal, and a zeolitic support; wherein the first metal and the second metal are different; wherein the first metal and the second metal are present in a total amount of from about 4 wt. % to about 0.8 wt. %, based on the total weight of the hydrogenolysis bimetallic supported catalyst; wherein the first metal comprises platinum (Pt), wherein Pt is present in a total amount of from about 0.2 wt. % to about 0.4 wt. %, based on the total weight of the hydrogenolysis bimetallic supported catalyst, wherein the second metal comprises Ir, wherein Ir is present in a total amount of from about 0.2 wt. % to about 0.4 wt. % based on the total weight of the hydrogenolysis bimetallic supported catalyst; wherein Pt and Ir are present in a weight ratio of Pt to Ir of from about 0.8:1 to about 1.2:1; wherein the zeolite support comprises ZSM-5; and wherein the zeolitic support is characterized by a weight ratio of silica to alumina (SiO 2 /Al 2 O 3 ) of from about 250 to about 300.

2. The hydrogenolysis bimetallic supported catalyst of claim 1 ; wherein the zeolitic support comprises an additional zeolite and/or a binder; wherein the additional zeolite is selected from the group consisting of ZSM-11, Y, high-silica Y, USY, EU-1, EU-2, beta, L, ferrierite, CHA, SSZ-16, Nu-3, Sigma-1, Silicalite-1, and combinations thereof; and wherein the binder comprises alumina, titania, silica, or combinations thereof.

3. The hydrogenolysis bimetallic supported catalyst of claim 1 , wherein the zeolitic support is characterized by a weight ratio of silica to alumina (SiO 2 /Al 2 O 3 ) of about 280.

4. A method of making a hydrogenolysis bimetallic supported catalyst comprising:
(a) contacting a zeolitic support with an aqueous metal precursor solution to form a bimetallic impregnated zeolitic support, wherein the aqueous metal precursor solution comprises a first metal precursor and a second metal precursor, and wherein the aqueous metal precursor solution is characterized by a weight ratio of Pt to IR of from about 0.8:1 to about 1.2:1;
(b) drying the bimetallic impregnated zeolitic support at a temperature of from about 70° C. to about 180° C. to form a dry bimetallic impregnated zeolitic support;
(c) calcining the dry bimetallic impregnated zeolitic support under an oxidizing atmosphere at a temperature of from about 200° C. to about 550° C. to form a calcined bimetallic impregnated zeolitic support; and
(d) reducing the Pt and the Ir to form the hydrogenolysis bimetallic supported catalyst of claim 1 .

5. The method of claim 4 , wherein the step (d) of reducing the Pt and the Ir comprises contacting the calcined bimetallic impregnated zeolitic support with a reducing medium at a temperature of from about 300° C. to about 500° C.

6. The method of claim 5 , wherein the reducing medium comprises hydrogen, and optionally a hydrocarbon and/or carbon monoxide.

7. The method of claim 6 , wherein the calcined bimetallic impregnated zeolitic support is contacted with hydrogen at a temperature of from about 300° C. to about 500° C.

8. The method of claim 4 , wherein the step (d) of reducing the Pt and the Ir comprises contacting the first metal precursor and/or the second metal precursor with a reducing medium.

9. The method of claim 8 , wherein steps (a) and (d) occur about concurrently.

10. The method of claim 4 , wherein step (a) comprises co-impregnating the zeolitic support with the first metal precursor and the second metal precursor.

11. The method of claim 4 , wherein step (a) comprises (i) contacting a zeolitic support with a first aqueous metal precursor solution to form a monometallic impregnated zeolitic support, wherein the first aqueous metal precursor solution comprises the first metal precursor; and (ii) contacting the monometallic impregnated zeolitic support with a second aqueous metal precursor solution to form the bimetallic impregnated zeolitic support, wherein the second aqueous metal precursor solution comprises the second metal precursor.

12. The method of claim 4 , wherein the dry bimetallic impregnated zeolitic support is calcined for a time period of from about 30 minutes to about 72 hours.

13. A process for selective hydrogenolysis comprising introducing a butane feed stream and hydrogen to a hydrogenolysis reactor to produce a hydrogenolysis product stream, wherein the hydrogenolysis reactor comprises the hydrogenolysis bimetallic supported catalyst of claim 1 , wherein the hydrogenolysis reactor is characterized by a temperature of from about 200° C. to about 330° C., wherein the butane feed stream comprises n-butane and i-butane, wherein the hydrogenolysis product stream comprises hydrogen, methane, ethane, propane, i-butane, and optionally n-butane; and wherein the hydrogenolysis reactor is characterized by an i-butane conversion that is less than an n-butane conversion.

14. The process of claim 13 , wherein the hydrogenolysis reactor is characterized by a pressure of from about 0 psig to about 300 psig; a hydrocarbon-based weight hourly space velocity (WHSV) of from about 0.1 h −1 to about 15 h −1 ; and a hydrogen to C 4 hydrocarbons molar ratio of from about 0.1:1 to about 10:1.

15. The process of claim 13 , wherein the hydrogenolysis reactor is characterized by an i-butane conversion of less than about 25%; and/or wherein the hydrogenolysis reactor is characterized by a n-butane conversion of equal to or greater than about 90%.

16. The process of claim 13 , wherein the hydrogenolysis bimetallic supported catalyst is characterized by (i) a selectivity to ethane of from about 60 mol % to about 90 mol %; (ii) a selectivity to methane of less than about 20 mol %; (iii) a selectivity to propane of less than about 15 mol %; or (iv) any combinations of (i)-(iii).

17. The hydrogenolysis bimetallic supported catalyst of claim 1 , wherein Pt is present in a total amount of about 0.3 wt. %, based on the total weight of the hydrogenolysis bimetallic supported catalyst; wherein Ir is present in a total amount of about 0.3 wt. %, based on the total weight of the hydrogenolysis bimetallic supported catalyst; and wherein the zeolitic support is characterized by a weight ratio of silica to alumina (SiO 2 /Al 2 O 3 ) of about 280.

18. The method of claim 7 , wherein the calcined bimetallic impregnated zeolitic support is contacted with hydrogen at a temperature of from about 350° C. to about 450° C., and for a time period of from about 30 minutes to about 8 hours.

19. The process of claim 13 , wherein the hydrogenolysis reactor is characterized by an i-butane conversion of less than about 15%, and wherein the hydrogenolysis reactor is characterized by a n-butane conversion of equal to or greater than about 95%.

20. The process of claim 1 , wherein Pt and Ir are present in a weight ratio of Pt to Ir of about 1:1.

Assignees

• Sabic Global Technologies Bv

Inventors

• Dasari Prasanna
• Myint Myatnoezin
• Barton Katherine
• Kulkarni Neeta
• Ghosh Ashim
• Pelaez Raul Velasco
• Fickel Dustin
• Shou Heng

Classifications

• B01J37/0209

  involving a reaction between the support and a fluid · CPC title

• B01J29/7215

  Zeolite Beta · CPC title

• B01J29/035

  {Microporous crystalline materials not having base exchange properties, such as} silica polymorphs, e.g. silicalites · CPC title

• C07C2529/44

  Noble metals · CPC title

• B01J6/001

  Calcining · CPC title