Ethanol manufacturing process over catalyst having improved radial crush strength

Patent metadata

Field	Value
Publication number	US-9486781-B2
Application number	US-201414492695-A
Country	US
Kind code	B2
Filing date	Sep 22, 2014
Priority date	Mar 13, 2012
Publication date	Nov 8, 2016
Grant date	Nov 8, 2016

Abstract

Acetic acid is hydrogenation in the presence of a catalyst comprising one or more active metals on a silica support, wherein the catalyst has a radial crush strength of at least 4 N/mm. The one or more active metals may include cobalt, copper, gold, iron, nickel, palladium, platinum, iridium, osmium, rhenium, rhodium, ruthenium, tin, zinc, lanthanum, cerium, manganese, chromium, vanadium, molybdenum and mixtures thereof. Radial crush strength may be improved by steam treating the catalyst support prior to the loading of the one or more active metals.

First claim

We claim:

1. A hydrogenation catalyst for converting acetic acid to ethanol, the catalyst comprising:
one or more active metals on a silica support, wherein the one or more active metals is selected from the group consisting of cobalt, copper, gold, iron, nickel, palladium, platinum, iridium, osmium, rhenium, rhodium, ruthenium, tin, zinc, lanthanum, cerium, manganese, chromium, vanadium, molybdenum and mixtures thereof,
wherein the catalyst has a radial crush strength of at least 4 N/mm.

2. The catalyst of claim 1 , wherein the silica support is subjected to steam treatment at a temperature above 50° C. for a period of time prior to impregnating the one or more metals on the silica support.

3. The catalyst of claim 1 , wherein the catalyst is made by:
providing a dry support selected from the group consisting of silica, silica/alumina, calcium metasilicate, pyrogenic silica, high purity silica, and mixtures thereof;
subjecting the dry support to treatment with steam at a temperature from 50° C. to 300° C. for a period of time from 0.1 to 200 hours;
drying the support such that the support comprises at least 0.5% moisture after treatment; and
impregnating the support with the one or more active metals.

4. The catalyst of claim 3 , further comprising calcining the catalyst at a temperature from 250° C. to 800° C., optionally for a period from 1 to 12 hours.

5. The catalyst of claim 1 , wherein the radial crush strength is from 4 N/mm to 12 N/mm.

6. The catalyst of claim 1 , wherein the silica support has an average particle size from 0.01 to 1.0 cm.

7. The catalyst of claim 1 , wherein the support material has a surface area from 50 to 600 m 2 /g.

8. The catalyst of claim 1 , wherein the silica support is selected from the group consisting of silica, silica/alumina, calcium metasilicate, pyrogenic silica, high purity silica, or mixtures thereof.

9. The catalyst of claim 1 , wherein the one or more active metals is selected from the group consisting of palladium, iron, cobalt, platinum, tin and combinations thereof.

10. The catalyst of claim 1 , wherein the support material is present in an amount from 25 to 99 wt. %, based on the total weight of the catalyst composition.

11. The catalyst of claim 1 , wherein the support material further comprises a support modifier, wherein the support modifier is present in an amount from 0.1 to 50 wt. %, based on the total weight of the catalyst composition.

12. The catalyst of claim 11 , wherein the support modifier is selected from the group consisting of (i) alkaline earth metal oxides, (ii) alkali metal oxides, (iii) alkaline earth metal metasilicates, (iv) alkali metal metasilicates, (v) Group IIB metal oxides, (vi) Group IIB metal metasilicates, (vii) Group IIIB metal oxides, (viii) Group IIIB metal metasilicates, and mixtures thereof.

13. The catalyst of claim 11 , wherein the support modifier is calcium metasilicate or calcium oxide.

14. The catalyst of claim 11 , wherein the support modifier is selected from the group consisting of WO 3 , ZrO 2 , Nb 2 O 5 , Ta 2 O 5 , Al 2 O 3 , B 2 O 3 , P 2 O 5 , Sb 2 O 3 , MoO 3 , Fe 2 O 3 , Cr 2 O 3 , V 2 O 5 , MnO 2 , CuO, Co 2 O 3 , Bi 2 O 3 , and combinations thereof.

15. The catalyst of claim 3 , wherein the treatment with steam is at a temperature from 50° C. to 150° C.

16. The catalyst of claim 3 , wherein the treatment with steam is at a partial pressure from 100 to 5,000 kPa.

17. The catalyst of claim 3 , wherein the weight of the silica support increases by at least 0.0001% during the treatment with steam.

18. The catalyst of claim 3 , wherein the weight of the silica support increases by at least 20% during the treatment with steam.

19. The catalyst of claim 3 , wherein the support comprises from 0.5 to 33% moisture after the drying.

Assignees

• Celanese Int Corp

Inventors

• Zhou Zhenhua
• Duff Emily
• Kumar Dheeraj
• Weiner Heiko

Classifications

• B01J35/37

  Crush or impact strength · CPC title

• C07C29/149

  with hydrogen or hydrogen-containing gases · CPC title

• B01J21/04

  Alumina · CPC title

• C07C31/08

  Ethanol · CPC title

• B01J23/42

  Platinum · CPC title