Catalyst for oxidative dehydrogenation and method of preparing the same

Patent metadata

Field	Value
Publication number	US-10994262-B2
Application number	US-201715765445-A
Country	US
Kind code	B2
Filing date	May 18, 2017
Priority date	Jun 7, 2016
Publication date	May 4, 2021
Grant date	May 4, 2021

Abstract

Disclosed are a catalyst for oxidative dehydrogenation and a method of preparing the same. More particularly, a catalyst for oxidative dehydrogenation of butene having a high butene conversion rate and superior side reaction inhibition effect and thus having high reactivity and high selectivity for a product by preparing metal oxide nanoparticles and then fixing the prepared metal oxide nanoparticles to a support, and a method of preparing the same are provided.

First claim

The invention claimed is:

1. A catalyst for oxidative dehydrogenation, comprising:
a support consisting of one or more selected from the group consisting of silica, cordierite, titania, zirconia, silicon nitride, and silicon carbide; and
a plurality of metal oxide particles having a composition of Formula 1 below and an average particle diameter of 0.1 to 50 nm uniformly coated or distributed on a surface of the support:
AB 2 O 4   [Formula 1]

wherein A is one or more selected from the group consisting of Cu, Ra, Ba, Sr, Ca, Be, Zn, and Mg, and B is one or more selected from the group consisting of trivalent cationic metals, and
wherein the metal oxide particles are included in an amount of 5 to 20 parts by weight based on 100 parts by weight of the support, and
wherein the catalyst exhibits selectivity for butadiene in an oxidative dehydrogenation conversion of butene and inhibits generation of CO and/or CO 2 as a byproduct.

2. The catalyst according to claim 1 , wherein B is one or more selected from the group consisting of Al, Fe(III), Cr, V, Ga, In, La, and Ce.

3. The catalyst according to claim 1 , wherein the catalyst is a supporting catalyst or a coating catalyst.

4. A method of preparing a catalyst for oxidative dehydrogenation, wherein the method is performed by supporting or coating a nano-scale metal oxide on a support consisting of one or more selected from the group consisting of silica, cordierite, titania, zirconia, silicon nitride, and silicon carbide, the method comprising:
obtaining a mixed solution by mixing a precursor of divalent cationic metals (A), a precursor of trivalent cationic metals (B), an unsaturated fatty acid, a surfactant, and an organic solvent that is one or more selected from the group consisting of hexadecane, hexadecene, octadecane, octadecene, and octyl ether; and
heating the mixed solution by elevating a temperature up to 100° C. to 120° C. at a temperature elevation rate of 1 to 10° C./min and maintaining the elevated temperature for 30 minutes to 1 hour to remove water and oxygen, followed by elevating the temperature up to 190° C. to 210° C. at a temperature elevation rate of 1 to 10° C./min and maintaining the elevated temperature for 1 hour to 2 hours, and subsequently heating up to 290° C. to 310° C. at a temperature elevation rate of 1 to 5° C./min, and then refluxing for 1 hour to 2 hours to prepare the nano-scale metal oxide having a composition of Formula 1 below and an average particle diameter of 0.1 to 50 nm:
AB 2 O 4   [Formula 1]

wherein A is one or more selected from the group consisting of Cu, Ra, Ba, Sr, Ca, Be, Zn, and Mg, and B is one or more selected from the group consisting of trivalent cationic metals;
dispersing the nano-scale metal oxide in a solvent having a boiling point of 69° C. or less to form a dispersion of the nano-scale metal oxide;
coating the dispersion of the nano-scale metal oxide on the support; and
drying the support coated with the dispersion of the nano-scale metal oxide at a temperature of 40° C. to 60° C.

5. The method according to claim 4 , wherein the divalent cationic metal (A) precursor is selected from the group consisting of zinc acetate, zinc acetylacetonate, magnesium acetate, and magnesium acetylacetonate.

6. The method according to claim 4 , wherein the trivalent cationic metal (B) precursor is selected from the group consisting of aluminum acetate, aluminum acetylacetonate, iron acetate, iron acetylacetonate, chromium acetate, and chromium acetylacetonate.

7. The method according to claim 4 , wherein the divalent cationic metal (A) precursor and the trivalent cationic metal (B) precursor are mixed in a molar ratio (B/A) of 1.5 to 3.

8. The method according to claim 4 , wherein the unsaturated fatty acid is one or more selected from the group consisting of lauric acid, palmitic acid, oleic acid, and stearic acid.

9. The method according to claim 4 , wherein the surfactant is one or more selected from the group consisting of octylamine, trioctylamine, decylamine, dodecylamine, tetradecylamine, hexadecylamine, oleylamine, octadecylamine, tribenzylamine, and triphenylamine.

10. The method according to claim 4 , wherein a molar ratio of the unsaturated fatty acid to the surfactant is 1:1 to 10:1.

11. The method according to claim 4 , wherein the solvent having a boiling point of 69° C. or less is hexane or methylpentane.

Assignees

• Lg Chemical Ltd

Inventors

• Kim Seongmin
• Ko Dong Hyun
• Cha Kyong Yong
• Choi Dae Heung
• Suh Myung Ji
• Han Jun Kyu
• Hwang Sun Hwan
• Kang Jun Han
• Lee Joo Hyuck
• Nam Hyun Seok
• Hwang Ye Seul
• Han Sang Jin

Classifications

• C07C5/48

  with oxygen as an acceptor · CPC title

• B01J35/40

  characterised by dimensions, e.g. grain size (in a colloidal state B01J35/23; crystallite size B01J35/77) · CPC title

• B01J23/745 Primary

  Iron · CPC title

• B01J35/45

  Nanoparticles · CPC title

• B01J2235/30

  Scanning electron microscopy; Transmission electron microscopy · CPC title