Method for the production of ethyleneamines

Patent metadata

Field	Value
Publication number	US-11208373-B2
Application number	US-201816619976-A
Country	US
Kind code	B2
Filing date	May 24, 2018
Priority date	Jun 9, 2017
Publication date	Dec 28, 2021
Grant date	Dec 28, 2021

Abstract

The present invention relates to a process for preparing alkanolamines and/or ethyleneamines in the liquid phase, by reacting ethylene glycol and/or monoethanolamine with ammonia in the presence of an amination catalyst comprising Co, Ru and Sn.

First claim

The invention claimed is:

1. A process for preparing alkanolamines and/or ethyleneamines in the liquid phase, by reacting ethylene glycol and/or monoethanolamine with ammonia in the presence of an amination catalyst comprising Co, Ru and Sn and
wherein the catalyst is prepared by the reduction of a catalyst precursor and the preparation of the catalytic precursor consists essentially of the steps of
(i) Contacting a catalytic support material with one or more soluble compounds of active metals and optionally one or more soluble compounds of additional catalytic elements with a solution comprising such compounds;
(ii) Optionally, working up the catalyst precursor comprising the steps of separating the catalytic precursor from the solution and optionally washing and drying the separated catalytic precursor;
(iii) Subjecting the separated catalytic precursor to a reductive calcination step;
and wherein steps (i) and (ii) can be repeated one or more times before performing step (iii).

2. The process according to claim 1 , wherein the catalyst precursor comprises
0.01% to 20% by weight of catalytically active components of Ru, calculated as RuO; and
1% to 50% by weight of catalytically active components of Co, calculated as CoO; and
0.1% to 5% by weight of catalytically active components of Sn, calculated as SnO.

3. The process according to claim 1 , wherein the catalyst precursor comprises one or more added catalyst elements selected from the group consisting of Cu, Ni, Zr and AI.

4. The process according to claim 3 , wherein the catalyst precursor comprises
(i) 0.2% to 5% by weight of catalytically active components of Sn, calculated as SnO,
(ii) 1% to 35% by weight of catalytically active components of Co, calculated as CoO,
(iii) 10% to 80% by weight of catalytically active components of Al and/or Zr, calculated as Al 2 O 3 and ZrO 2 respectively;
(iv) 1% to 35% by weight of catalytically active components of Cu and/or 1% to 35% by weight of catalytically active components of Ni, calculated as CuO and NiO respectively; and
(v) 0.01% to 20% by weight of catalytically active components of Ru, calculated as RuO.

5. The process according to claim 1 , wherein the catalyst precursor is prepared by coprecipitation.

6. The process according to claim 1 , wherein the catalyst precursor is prepared by precipitative application or impregnation.

7. The process according to claim 1 , wherein the catalyst precursor is prepared by precipitative application or coprecipitation and is impregnated in a further step.

8. The process according to claim 7 , wherein a catalyst precursor comprising only with a portion of the active metals Ru, Co and Sn is prepared by coprecipitation or precipitative application and the missing active metals or the missing portion of the active metals are applied to the catalyst precursor in a subsequent impregnation step.

9. The process according to claim 8 , wherein a catalyst precursor comprising the active metals Co and Sn is first prepared and is then contacted in a further impregnation step with the active metals Co and Ru.

10. The process according to claim 9 , wherein a catalyst precursor is prepared by precipitative application of the soluble compounds of Co and Sn to a support material and the catalyst precursor thus obtained is contacted with a soluble compound of Ru and a soluble compound of Co in an impregnation step.

11. The process according to claim 10 , wherein Sn nitrate and Co nitrate are precipitated onto a support material in the presence of complexing agents and the catalyst precursor thus obtained is contacted with a soluble compound of Ru and a soluble compound of Co in an impregnation step.

12. The process according to claim 1 , which further the reductive calcination is in the presence of hydrogen and an inert gas.

13. The process according to claim 12 , wherein hydrogen is present in an amount from 1 to at most 50% by volume.

14. A process for preparing alkanolamines and/or ethyleneamines in the liquid phase, by reacting ethylene glycol and/or monoethanolamine with ammonia in the presence of an amination catalyst comprising Co, Ru and Sn and wherein a catalyst precursor is reductively calcined and wherein the catalyst precursor comprises
0.01% to 20% by weight of catalytically active components of Ru, calculated as RuO;
1% to 50% by weight of catalytically active components of Co, calculated as CoO; and
0.1% to 5% by weight of catalytically active components of Sn, calculated as SnO.

15. A process for preparing alkanolamines and/or ethyleneamines in the liquid phase, by reacting ethylene glycol and/or monoethanolamine with ammonia in the presence of an amination catalyst comprising Co, Ru and Sn and
wherein the catalyst is prepared by the reduction of a catalyst precursor and the preparation of the catalytic precursor comprising the steps of
(i) Contacting a catalytic support material with one or more soluble compounds of active metals and optionally one or more soluble compounds of additional catalytic elements with a solution comprising such compounds;
(ii) Optionally working up the catalyst precursor comprising the steps of separating the catalytic precursor from the solution and optionally washing and drying the separated catalytic precursor;
(iii) Subjecting the separated catalytic precursor to a reductive calcination step;
and wherein steps (i) and (ii) can be repeated one or more times before performing step (iii) and with the proviso that an oxidative calcination step conducted in the presence of oxidizing gases is excluded after step (i) or step (ii), respectively.

16. The process according to claim 14 , wherein the catalyst precursor comprising only with a portion of the active metals Ru, Co and Sn is prepared by coprecipitation or precipitative application and the missing active metals or the missing portion of the active metals are applied to the catalyst precursor in a subsequent impregnation step.

17. The process according to claim 1 , wherein the reductive calcination step is conducted in the presence of inert gas at temperature from 200 to 300° C.

18. The process according to claim 15 , wherein the reductive calcination step is conducted in the presence of inert gas at temperature from 200 to 300° C.

19. The process according to claim 14 , wherein the catalyst precursor comprises a support material.

20. The process according to claim 19 , wherein the support material is aluminum oxide, zirconium oxide or mixtures thereof.

21. The process according to claim 20 , wherein the median diameter d 50 of the support material particles is in the range from 1 to 500 μm.

Assignees

• Basf Se

Inventors

• Heidemann Thomas
• Becker Barbara
• Koch Eva
• Melder Johann-Peter
• Luyken Hermann

Classifications

• B01J2235/00

  Indexing scheme associated with group B01J35/00, related to the analysis techniques used to determine the catalysts form or properties · CPC title

• B01J35/50

  characterised by their shape or configuration · CPC title

• C07C209/16 Primary

  with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings · CPC title

• B01J37/0236

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

• B01J37/088

  Decomposition of a metal salt · CPC title