Method for producing transition alumina catalyst monoliths

Patent metadata

Field	Value
Publication number	US-11547981-B2
Application number	US-201915733841-A
Country	US
Kind code	B2
Filing date	May 28, 2019
Priority date	May 29, 2018
Publication date	Jan 10, 2023
Grant date	Jan 10, 2023

Abstract

A method for producing a three-dimensional porous transition alumina catalyst monolith of stacked catalyst fibers, comprising:a) Preparing a paste in a liquid diluent of hydroxide precursor particles and/or oxyhydroxide precursor particles of transition alumina particles, all particles in the suspension having a number average particle size in the range of from 0.05 to 700 μm,b) extruding the paste nozzle(s) to form fibers, and depositing the extruded fibers to form a three-dimensional porous catalyst monolith precursor,c) drying the precursor to remove the liquid diluent,d) performing a temperature treatment of the dried porous catalyst monolith precursor to form the transition alumina catalyst monolith,wherein no temperature treatment of the porous catalyst monolith precursor or porous catalyst monolith at temperatures above 1000° C. is performed and wherein no further catalytically active metals, metal oxides or metal compounds are applied to the surface.

First claim

The invention claimed is:

1. A method for producing a three-dimensional porous transition alumina catalyst monolith of stacked catalyst fibers, comprising the following steps:
a) preparing a suspension paste in a liquid diluent of hydroxide precursor particles or oxy-hydroxide precursor particles of transition alumina particles or mixtures thereof and which suspension can furthermore comprise a binder material selected from organic materials in a maximum amount of 20 wt %, based on the amount of hydroxide precursor particles or oxyhydroxide precursor particles of transition alumina particles or mixtures thereof and/or a plasticizer chosen from organic materials in a maximum amount of 10 wt %, based on the amount of hydroxide precursor particles or oxyhydroxide precursor particles of transition alumina particles or mixtures thereof, all particles in the suspension having a number average particle size in the range of from 0.05 to 700 μm,
b) extruding the paste of step a) through one or more nozzles to form fibers, and depositing the extruded fibers to form a three-dimensional porous catalyst monolith precursor,
c) drying the porous catalyst monolith precursor to remove the liquid diluent,
d) performing a temperature treatment of the dried porous catalyst monolith precursor of step c) at a temperature in the range of from 500 to 1000° C., to form the transition alumina catalyst monolith,
wherein no temperature treatment of the porous catalyst monolith precursor or porous catalyst monolith at temperatures above 1000° C. is performed and
wherein no further catalytically active metals, metal oxides or metal compounds are applied to the surface of the transition alumina precursor particles, the catalyst monolith precursor or transition alumina catalyst monolith,
wherein no dopants are added to the suspension paste and
wherein the amount of impurities, selected from Li 2 O, Na 2 O, K 2 O, CaO, MgO, BaO, B 2 O 3 , Ga 2 O 3 , SiO 2 , TiO 2 , ZrO 2 , ZnO, Fe 2 O 3 , as well as chlorides, nitrates and sulfates in the transition alumina particles and hydroxide precursor particles and oxyhydroxide precursor particles thereof, is not higher than 2.5 wt %, based on the transition alumina in the monolith.

2. The method of claim 1 , wherein transition alumina is the sole phase forming the catalyst monolith.

3. The method of claim 1 , wherein the transition alumina is eta-, gamma- or delta-alumina, and wherein eta-, gamma- and/or delta-alumina particles are present in the suspension paste; and/or wherein gibbsite, bayerite, nordstrandite, doyleite, diaspore, boehmite, pseudoboehmite, akdalaite or tohdite, or mixtures thereof are present in the suspension paste and wherein in step d) a temperature treatment in the range of from 500 to 925° C. is performed to effect the transformation.

4. The method of claim 1 , wherein in step b) the nozzles have a maximum diameter of less than 5 mm.

5. The method of claim 1 , wherein the monolith of stacked catalyst fibers is three-dimensionally structured by depositing the extruded fibers in a regular, recurring stacking pattern to form a three-dimensionally structured porous catalyst monolith precursor.

6. The method of claim 1 , wherein the monolith is formed from one continuous extruded fiber or from multiple individual extruded fibers.

7. The method of claim 1 , wherein the regular, recurring stacking pattern is composed of stacked layers of extruded fibers, wherein in each layer at least 50 wt % of the extruded fibers are deposited parallel to each other and spatially separated from each other, or in a cobweb pattern.

8. The method according to claim 7 , wherein at least 50 wt % of the extruded fibers are deposited as linear strands parallel to each other and spatially separated from each other, or wherein multiple cobweb patterns are stacked, wherein the direction of the strands in each layer is different from the direction in neighboring layers, so that a porous structure with contact points of strands of neighboring layers results.

9. The method according to claim 1 , wherein the transition alumina particles, hydroxide precursor particles or oxyhydroxide precursor particles or mixtures thereof or the transition alumina catalyst monolith have an acidity in the range of from 100 to 2000 μmol/g.

10. The method according to claim 1 , wherein the transition alumina catalyst monolith consists of eta-, gamma- or delta-alumina, or mixtures thereof.

11. The method of claim 1 , wherein the transition alumina catalyst monolith has a BET surface area in the range of from 50 to 350 m 2 /g.

12. The method according to claim 1 , wherein the transition alumina catalyst monolith has a porosity of at least 20%, determined by nitrogen physisorption.

13. The method according to claim 1 , wherein the transition alumina catalyst monolith has a pore volume in the range of from 0.05 to 2.0 ml/g, determined by mercury porosimetry measurements.

14. The method according to claim 1 , wherein the transition alumina catalyst monolith contains no dopants and the content of impurities is below 0.1 wt %.

15. The method according to claim 1 , wherein the transition alumina catalyst monolith has a monomodal or polymodal pore size distribution.

16. A three-dimensional porous catalyst monolith of stacked catalyst fibers, obtainable by the method according to claim 1 .

17. The monolith according to claim 16 , which has a side crushing strength of at least 60 N, determined as disclosed in Oil and Gas Science and Technology-Riv. IFP, vol 55 (2000) No 1, pages 67-85.

18. A dehydration reaction which comprises utilizing the three-dimensional porous transition alumina catalyst monolith of stacked catalyst fibers according to claim 16 .

19. The reaction according to claim 18 , wherein methanol, ethanol, n-propanol, iso-propanol, n-butanol, iso-butanol, tert-butanol, pentanol, hexanol, 1-phenylethanol, 2-phenylethanol, cumyl alcohol (2-phenyl-2-propanol) or glycerol are dehydrated.

20. A process for the isomerization of double bonds, cis/trans isomerization and skeletal isomerization reactions utilizing the three-dimensional porous transition alumina catalyst monolith of stacked catalyst fibers according to claim 16 .

21. A method for producing a three-dimensional porous transition alumina catalyst monolith of stacked catalyst fibers, comprising the following steps:
a) preparing a suspension paste in a liquid diluent of hydroxide precursor particles or oxy-hydroxide precursor particles of transition alumina particles or mixtures thereof and which suspension can furthermore comprise a binder material selected from organic materials in a maximum amount of 20 wt %, based on the amount of hydroxide precursor particles or oxyhydroxide precursor particles of transition alumina particles or mixtures thereof and/or a plasticizer chosen from organic materials in a maximum amount of 10 wt %, based on the amount of hydroxide precursor particles or oxyhydroxide precursor particles of transition alumina particles or mixtures thereof, all particles in the suspension having a number average particle size in the range of from 0.05 to 700 μm,
b) extruding the paste of step a) through one or more nozzles to form fibers, and depositing the extruded fibers to form a three-dimensional porous catalyst monolith precursor,
c) drying the porous catalyst monolith precursor to remove the liquid diluent,
d) performing a temperature treatment of the dried porous catalyst monolith precursor of step c) at a temperature in the range of from 500 to 100

Assignees

• Basf Se

Inventors

• Schwab Matthias Georg
• Groeneveld Esther
• Berben Peter
• Bouwman Harry
• Dijkstra Willem
• Michielsen Bart
• Lefevere Jasper

Classifications

• C04B2235/5409

  expressed by specific surface values · CPC title

• B01J37/00

  Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts · CPC title

• C04B2111/0081

  as catalysts or catalyst carriers · CPC title

• B28B1/001

  Rapid manufacturing of 3D objects by additive depositing, agglomerating or laminating of material (selective deposition modelling of metallic powder B22F10/00; rapid manufacturing of 3D objects in general and in particular of plastics B29C64/00) · CPC title

• C04B2235/349

  Clays, e.g. bentonites, smectites such as montmorillonite, vermiculites or kaolines, e.g. illite, talc or sepiolite · CPC title