Shaped porous carbon products

Patent metadata

Field	Value
Publication number	US-10654027-B2
Application number	US-201916520869-A
Country	US
Kind code	B2
Filing date	Jul 24, 2019
Priority date	Apr 29, 2014
Publication date	May 19, 2020
Grant date	May 19, 2020

Abstract

Shaped porous carbon products and processes for preparing these products are provided. The shaped porous carbon products can be used, for example, as catalyst supports and adsorbents. Catalyst compositions including these shaped porous carbon products, processes of preparing the catalyst compositions, and various processes of using the shaped porous carbon products and catalyst compositions are also provided.

First claim

What is claimed is:

1. A catalyst composition comprising a shaped porous carbon product as a catalyst support and a catalytically active component or precursor thereof, wherein the shaped porous carbon product comprises:
(a) carbon black and
(b) a carbonized binder comprising a carbonization product of a binder comprising a saccharide selected from the group consisting of a monosaccharide, a disaccharide, an oligosaccharide, and combinations thereof and wherein the shaped porous carbon product has a BET specific surface area from about 20 m 2 /g to about 500 m 2 /g.

2. The catalyst composition of claim 1 , wherein the binder comprises a monosaccharide selected from the group consisting of glucose, fructose, hydrate thereof, syrup thereof, and combinations thereof.

3. The catalyst composition of claim 1 , wherein the binder further comprises a polymeric carbohydrate, derivative of a polymeric carbohydrate, or a non-carbohydrate synthetic polymer, or any combination thereof.

4. The catalyst composition of claim 1 , wherein the binder further comprises a cellulosic compound selected from the group consisting of methylcellulose, ethylcellulose, ethylmethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, methylhydroxyethylcellulose, ethylhydroxyethylcellulose, hydroxypropylmethylcellulose, carboxymethylcellulose, and mixtures thereof.

5. The catalyst composition of claim 1 , wherein the binder further comprises a starch.

6. The catalyst composition of claim 1 , wherein the binder further comprises a non-carbohydrate synthetic polymer selected from the group consisting of polyacrylic acid, polyvinyl alcohols, polyvinylpyrrolidones, polyvinyl acetates, polyacrylates, polyethers, and copolymers derived therefrom.

7. The catalyst composition of claim 1 , wherein the binder comprises a saccharide selected from the group consisting of glucose, fructose, hydrates thereof and combinations thereof and a polymeric carbohydrate or derivative of the polymeric carbohydrate selected from the group consisting of hydroxyethylcellulose, methylcellulose, starch and combinations thereof.

8. The catalyst composition of claim 7 , wherein the weight ratio of (i) the saccharide to (ii) the polymeric carbohydrate or derivative of the polymeric carbohydrate is from about 5:1 to about 50:1.

9. The catalyst composition of claim 1 , wherein the catalytically active component or precursor thereof comprises a metal selected from the group consisting of cobalt, nickel, copper, zinc, iron, vanadium, molybdenum, manganese, barium, ruthenium, rhodium, rhenium, palladium, silver, osmium, iridium, platinum, gold, and combinations thereof.

10. The catalyst composition of claim 9 , wherein the metal comprises platinum.

11. The catalyst composition of claim 1 , wherein the shaped porous carbon product has:
(a) a mean diameter of at least about 50 μm;
(b) a BET specific surface area from about 20 m 2 /g to about 350 m 2 /g;
(c) a mean pore diameter from about 5 nm to about 100 nm;
(d) a pore size distribution such that the peak of the distribution is at a diameter greater than about 5 nm, but less than about 100 nm; and/or
(e) a specific pore volume of pores having a diameter of 1.7 nm to 100 nm as measured by the BJH method that is from about 0.1 cm 3 /g to about 1.5 cm 3 /g.

12. A process for the selective hydrodeoxygenation of aldaric acid or salt, ester, or lactone thereof to a dicarboxylic acid comprising reacting the aldaric acid or salt, ester, or lactone thereof with hydrogen in the presence of a halogen-containing compound and a catalyst composition of claim 1 to form the dicarboxylic acid.

13. The process of claim 12 , wherein the aldaric acid or salt, ester, or lactone thereof comprises glucaric acid or salt, ester, or lactone thereof and the dicarboxylic acid comprises adipic acid.

14. The process of claim 12 , wherein the halogen source comprises a hydrohalic acid.

15. The process of claim 12 , wherein the catalyst composition comprises at least one noble metal.

16. A process for the selective hydrodeoxygenation of 1,2,6-hexanetriol to 1,6-hexanediol comprising reacting the 1,2,6-hexanetriol with hydrogen in the presence of a catalyst composition of claim 1 to form 1,6-hexanediol.

17. The process of claim 16 , wherein the catalyst composition comprises platinum.

18. A process for the selective amination of 1,6-hexanediol to 1,6-hexamethylenediamine comprising reacting the 1,6-hexanediol with an amine in the presence of a catalyst composition of claim 1 to form 1,6-hexamethylenediamine.

19. The process of claim 18 , wherein catalyst composition comprises ruthenium.

20. The process of claim 19 , wherein the catalyst composition further comprises rhenium or nickel.

Assignees

• Archer Daniels Midland Co

Inventors

• Dias Eric L
• Hagemeyer Alfred
• Jiang Hong X
• Longmire James
• Shoemaker James A W
• Sokolovskii Valery
• Zhu Guang
• Murphy Vincent J
• Diamond Gary M

Classifications

• B01J23/40

  of the platinum group metals · CPC title

• C04B35/6365

  Cellulose or derivatives thereof · CPC title

• C04B2235/96

  Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance · CPC title

• C07C51/377

  by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups {(C07C51/36 - C07C51/373 take precedence)} · CPC title

• B01J23/22

  Vanadium · CPC title