Heterogeneous catalysts for the oxidative dehydrogenation of alkanes or oxidative coupling of methane

Patent metadata

Field	Value
Publication number	US-10407364-B2
Application number	US-201815993665-A
Country	US
Kind code	B2
Filing date	May 31, 2018
Priority date	Sep 9, 2015
Publication date	Sep 10, 2019
Grant date	Sep 10, 2019

Abstract

Improved methods of oxidative dehydrogenation (ODH) of short chain alkanes or ethylbenzene to the corresponding olefins, and improved methods of oxidative coupling of methane (OCM) to ethylene and/or ethane, are disclosed. The disclosed methods use boron- or nitride-containing catalysts, and result in improved selectivity and/or byproduct profiles than methods using conventional ODH or OCM catalysts.

First claim

We claim:

1. A method of making one or more desired chemical products comprising contacting a solid heterogeneous oxidative dehydrogenation (ODH) catalyst selected from the group consisting of a B-nitride consisting of boron and nitride, a B-nitride that is functionalized with one or more oxygen atoms bound directly to the B-nitride surface, a B-carbide consisting of boron and carbide, a B-carbide that is functionalized with one or more oxygen atoms bound directly to the B-carbide surface, Ti-boride, Ni-boride, and Nb-boride with a composition comprising both (a) oxygen and (b) one or more liquid or gaseous reactants to catalyze the ODH of the one or more liquid or gaseous reactants to form the one or more desired chemical products.

2. The method of claim 1 , wherein the one or more liquid or gaseous reactants include a C 3+ alkane or ethylbenzene.

3. The method of claim 2 , wherein the C 3+ alkane is a C 3 -C 5 n-alkane or a C 3 -C 5 iso-alkane.

4. The method of claim 1 , wherein the one or more liquid or gaseous reactants include an alkane or a hydrocarbon comprising an alkyl group, and wherein the one or more desired chemical products include one or more olefins or one or more hydrocarbons comprising an alkenyl group.

5. The method of claim 4 , wherein the alkane is a C 3 -C 5 n-alkane or a C 3 -C 5 iso-alkane.

6. The method of claim 5 , wherein the C 3 -C 5 n-alkane or C 3 -C 5 iso-alkane is selected from the group consisting of propane, n-butane, and isobutane, and wherein the one or more desired chemical products are selected from the group consisting of propene, isobutene, 1-butene, 2-butene and butadiene.

7. The method of claim 4 , wherein the method maintains a greater than 70% selectivity for the desired chemical products at 10% to 20% conversion of the alkane.

8. The method of claim 7 , wherein the method maintains a greater than 77% selectivity for the desired chemical products at 10% to 20% conversion of the alkane.

9. The method claim 4 , wherein the alkane is propane and the desired chemical product is propene.

10. The method of claim 4 , wherein the one or more desired chemical products further include ethylene.

11. The method of claim 10 , wherein the method exhibits a higher selectivity towards ethylene than it does towards undesired CO or CO 2 byproducts.

12. The method of claim 11 , wherein the method exhibits a 90% or greater selectivity for the ethylene and other desired products together.

13. The method of claim 4 , wherein the one or more liquid or gaseous reactants include a hydrocarbon comprising an alkyl group.

14. The method of claim 13 , wherein the hydrocarbon comprising an alkyl group is ethylbenzene, and wherein the one or more desired chemical products include styrene.

15. The method of claim 1 , wherein the ODH catalyst is functionalized with one or more oxygen atoms bound directly to the compound surface.

16. The method of claim 1 , wherein the ODH catalyst is a boron nitride consisting of boron and nitride or a boron nitride that is functionalized with one or more oxygen atoms bound directly to the boron nitride surface.

17. The method of claim 16 , wherein the boron nitride has a surface area range of about 5 m 2 g −1 to 550 m 2 g −1 , about 9 m 2 g −1 to 550 m 2 g −1 , about 50 m 2 g −1 to 550 m 2 g −1 , about 100 m 2 g −1 to 500 m 2 g −1 , or about 100 m 2 g −1 to 200 m 2 g −1 .

18. The method of claim 16 , wherein the boron nitride is in the form of hexagonal boron nitride (h-BN), boron nitride nanomeshes (h-BN nanomeshes), boron nitride nanosheets (BNNSs), boron nitride nanoribbons (BNNRs) or boron nitride nanotubes (BNNTs).

19. The method of claim 1 , wherein the solid heterogenous catalyst is not simultaneously contacted with nitrogen.

20. The method of claim 1 , wherein the composition comprising both (a) oxygen and (b) one or more liquid or gaseous reactants is a reactant stream that is contacted with the solid heterogeneous catalyst, and wherein the reactant stream includes from 0% to 70% nitrogen by volume.

Assignees

• Wisconsin Alumni Res Found

Inventors

• Hermans Ive
• Grant Joseph Thomas
• Carrero Marquez Carlos Alberto
• Chieregato Alessandro
• Venegas Juan Mauricio

Classifications

• C07C15/46

  Styrene; Ring-alkylated styrenes · CPC title

• C07C11/09

  Isobutene · CPC title

• C07C11/08

  with four carbon atoms · CPC title

• C07C11/06

  Propene · CPC title

• C07C11/04

  Ethene · CPC title