Catalyst for dehydrogenating hydrocarbons

Patent metadata

Field	Value
Publication number	US-10315970-B2
Application number	US-201515309029-A
Country	US
Kind code	B2
Filing date	May 6, 2015
Priority date	May 9, 2014
Publication date	Jun 11, 2019
Grant date	Jun 11, 2019

Abstract

The present invention relates to a catalyst based on iron oxide for the dehydrogenation of hydrocarbons and also a process for producing it. The catalyst comprises at least one iron compound, at least one potassium compound and at least one cerium compound, wherein the at least one iron compound and the at least one potassium compound are at least partly present in the form of one or more K/Fe mixed oxide phases of the general formula K x Fe y O z , where x is from 1 to 17; y is from 1 to 22 and z is from 2 to 34, where the catalyst comprises at least 20% by weight, based on the total catalyst, of the K/Fe mixed oxide phases and comprises crystalline cerium dioxide having a crystallite size in the range from 10 nm to 30 nm.

First claim

The invention claimed is:

1. A dehydrogenation catalyst comprising
from 50 to 90% by weight of at least one iron compound, calculated as Fe 2 O 3 ;
from 1 to 30% by weight of at least one potassium compound, calculated as K 2 O;
from 2 to 25% by weight of at least one cerium compound, calculated as CeO 2 ;
from 0.1 to 10% by weight of at least one magnesium compound, calculated as MgO;
from 0.1 to 10% by weight of at least one calcium compound, calculated as CaO; and
from 0 to 30% by weight of at least one further component,
wherein the at least one iron compound and the at least one potassium compound are at least partly present in the form of one or more K/Fe mixed oxide phases of the general formula
K x Fe y O z ,

where x is from 1 to 17; y is from 1 to 22 and z is from 2 to 34, where the catalyst comprises at least 40% by weight, based on the total catalyst, of the one or more K/Fe mixed oxide phases and comprises crystalline cerium dioxide having a crystallite size in the range from 16-19 nm.

2. The dehydrogenation catalyst according to claim 1 , wherein the catalyst comprises from 0.0001 to 10% by weight of at least one compound selected from compounds encompassing a metal selected from the group consisting of molybdenum, titanium, vanadium and tungsten, calculated as oxide in each case in the highest oxidation state, as further component.

3. The dehydrogenation catalyst according to claim 1 , wherein the catalyst comprises
from 50 to 90% by weight of at least one iron compound, calculated as Fe 2 O 3 ;
from 1 to 30% by weight of at least one potassium compound, calculated as K 2 O;
from 2 to 25% by weight of at least one cerium compound, calculated as CeO 2 ;
from 0.1 to 10% by weight of at least one magnesium compound, calculated as MgO;
from 0.1 to 10% by weight of at least one calcium compound, calculated as CaO;
from 0.1 to 10% by weight of at least one molybdenum compound, calculated as MoO 3 and
from 1 to 1000 ppm of at least one titanium compound, calculated as TiO 2 .

4. The dehydrogenation catalyst according to claim 1 , wherein the catalyst comprises at least 60% by weight, based on the total catalyst of the one or more K/Fe mixed oxide phases.

5. The dehydrogenation catalyst according to claim 3 , wherein the catalyst comprises at least 60% by weight, based on the total catalyst of the one or more K/Fe mixed oxide phases.

6. A process for producing a dehydrogenation catalyst according to claim 1 , which comprises the following steps)
i) producing a catalyst premix by mixing of at least one iron compound, at least one potassium compound, at least one cerium compound and optionally further metal compounds, optionally further components and optionally at least one binder with a solvent;
ii) producing shaped catalyst bodies from the catalyst premix obtained in step i); and
iii) drying of the shaped catalyst bodies and calcinations of the shaped catalyst bodies, where the calcinations of the shaped catalyst bodies is carried out at temperatures of from 700° C. to 850° C. and for a calcination time of from 15 minutes to 90 minutes, as a stationary process; or at temperatures of from 800 to 950° C. and for a calcination time of from 10 minutes to 30 minutes, as a continuous process.

7. The process for producing a dehydrogenation catalyst according to claim 6 , wherein the calcination in step iii) is carried out at temperatures of from 700° C. to 850° C. and for a calcination time of from 15 minutes to 90 minutes.

8. The process for producing a dehydrogenation catalyst according to claim 6 , wherein the calcination in step iii) is carried out at temperatures of from 800 to 950° C. and for a calcination time of from 10 minutes to 30 minutes.

9. A process for the catalytic dehydrogenation of a hydrocarbon, wherein a mixture of steam and at least one hydrocarbon is brought into contact with a dehydrogenation catalyst according to claim 1 .

10. The process for the catalytic dehydrogenation of a hydrocarbon according to claim 9 , wherein a mixture of steam and at least one hydrocarbon having a molar steam/hydrocarbon ratio in the range from 1 to 10 is used.

11. The process for catalytic dehydrogenation according to claim 9 , wherein the hydrocarbon is ethylbenzene.

Assignees

• Basf Se

Inventors

• Patcas Florina C
• Hinrichsen Bernd
• Dieterle Martin

Classifications

• B01J23/8898

  containing also molybdenum · CPC title

• C07C5/3332 Primary

  with metal oxides or metal sulfides · CPC title

• B01J37/08

  Heat treatment {(B01J37/0009, B01J37/0018 take precedence)} · CPC title

• B01J37/0009

  Use of binding agents; Moulding; Pressing; Powdering; Granulating; Addition of materials ameliorating the mechanical properties of the product catalyst · CPC title

• B01J37/04

  Mixing {(B01J37/0009, B01J37/0018 take precedence)} · CPC title