Post treated silver catalysts for epoxidation

Patent metadata

Field	Value
Publication number	US-10046311-B2
Application number	US-201615217564-A
Country	US
Kind code	B2
Filing date	Jul 22, 2016
Priority date	Jul 24, 2015
Publication date	Aug 14, 2018
Grant date	Aug 14, 2018

Abstract

The present disclosure generally relates to a silver-based epoxidation catalyst. In certain embodiments, a method is provided for modulating the reactivity of the silver-based epoxidation catalyst, comprising the catalyst being post-treated with at least two different salt solutions. In some embodiments, the treatment results in the deposition of one or more metals onto the surface of the catalyst. In further embodiments, method is also provided of using the silver catalyst to generate an epoxide from an olefin.

First claim

What is claimed is:

1. A catalyst comprising:
A) from about 45 to about 65 wt % of silver;
B) from about 0.0 to about 5.0 wt % of a catalyst promoter selected from the group consisting of molybdenum, tungsten, zinc, nickel, copper, scandium and ytterbium;
C) from 30 to about 90 wt % of a solid catalyst support selected from the group consisting of calcium titanate, magnesium titanate, barium titanate, strontium titanate, calcium carbonate, magnesium carbonate, barium carbonate, and strontium carbonate; and
D) from about 0.1 to about 6.5 wt % of a salt mixture comprising from about 0.25 to about 2.5 wt % of a first salt selected from the group consisting of potassium nitrate, silver nitrate, gallium nitrate, barium nitrate, magnesium nitrate, strontium nitrate, and calcium nitrate and from about 0.1 to about 4.0 wt % of a second salt selected from potassium nitrate and potassium carbonate, and wherein the salt mixture coats the silver component of step A), the solid catalyst support, or the catalyst promoter.

2. The catalyst of claim 1 , wherein the solid catalyst support is calcium carbonate.

3. A method for producing the catalyst of claim 1 comprising:
A) obtaining a solid catalyst support on which about 45 to about 65 wt % silver has been deposited, further comprising a catalyst promoter selected from the group consisting of molybdenum, tungsten, zinc, nickel, copper, scandium and ytterbium deposited on the solid catalyst support;
B) contacting the solid component of step A) with a first salt and a second salt, wherein the first salt is selected from the group consisting of potassium nitrate, silver nitrate, gallium nitrate, barium nitrate, magnesium nitrate, strontium nitrate, and calcium nitrate and the second salt is selected from potassium nitrate and potassium carbonate, in the presence of a solvent selected from the group consisting of water, methanol, ethanol and propanol for achieving the deposition of both metals; and
C) depositing from about 0.05 to about 2.5 wt % of the second salt and from about 0.05 to about 4.0 wt % of the first salt onto the solid catalyst support.

4. The method of claim 3 , wherein the solid catalyst support comprises from about 0.25 to about 2.5 wt % of the first salt deposited on the solid component.

5. The method of claim 3 , wherein the catalyst promoter is present at a concentration of from about 0 to about 5 wt %.

6. The method of claim 3 , wherein the deposition of the first salt and the second metal salt comprises a post-treatment after the catalyst promoter has been deposited on the silver deposited solid catalyst support.

7. The method of claim 3 , wherein step B) further comprises reacting the solid catalyst support with a chemical reducing agent selected from the group consisting of a sugar, aldehyde, hydrazine, metal hydride and phosphite salt to cause a chemical reduction of the deposited silver to elemental silver.

8. The method of claim 3 , wherein the catalyst is dried at a temperature of from about 100 to about 200° C.

9. The method of claim 3 , wherein the catalyst is calcinated at a temperature of from about 250 to about 500° C.

10. A method comprising reacting an alkene (C≤12) or aralkene (C≤12) in the presence of oxygen and the catalyst according to claim 1 to produce an epoxide (C≤12) .

Assignees

• Lyondell Chemical Tech Lp

Inventors

• Nagy Sandor
• Kimmich Barbara

Classifications

• B01J37/0201

  Impregnation · CPC title

• B01J37/0236

  Drying, e.g. preparing a suspension, adding a soluble salt and drying · CPC title

• B01J2523/00

  Constitutive chemical elements of heterogeneous catalysts · CPC title

• B01J23/8946

  with alkali or alkaline earth metals · CPC title

• B01J23/6567

  Rhenium · CPC title