IP Library Granted Patent US 7,169,730
Granted Patent B2
US 7,169,730 · App. 10/873,739 · Granted Jan 30, 2007

Modified carbide and oxycarbide containing catalysts and methods of making and using thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,169,730
App. No.
10/873,739
Granted
Jan 30, 2007
Kind
B2
Abstract

Compositions including modified carbide-containing nanorods and/or modified oxycarbide-containing nanorods and/or modified carbon nanotubes bearing carbides and oxycarbides and methods of making the same are provided. Rigid porous structures including modified oxycarbide-containing nanorods and/or modified carbide containing nanorods and/or modified carbon nanotubes bearing modified carbides and oxycarbides and methods of making the same are also provided. The compositions and rigid porous structures of the invention can be used either as catalyst and/or catalyst supports in fluid phase catalytic chemical reactions. Processes for making supported catalyst for selected fluid phase catalytic reactions are also provided.

Claims (19)

1. A method for the isomerization of a hydrocarbon comprising the step of: contacting a feed stream including a hydrocarbon under isomerization conditions with a composition, said composition including a plurality of nanostructures selected from the group consisting of carbon nanotubes, carbide nanorods, and mixtures thereof, each having a substantially uniform diameter between 1 nm and 100 nm and a length to diameter ratio greater than 5, said nanostructures further including a metal carbide selected from the group consisting of carbides and oxycarbides of a transition metal, rare earth metal or actinide, said composition having an ammonia desorption peak at a temperature greater than 100° C.

2. The method of claim 1 , wherein said hydrocarbon is selected from the group consisting of normal, branched, and cyclic hydrocarbons.

3. The method of claim 1 , wherein said hydrocarbon is an alkene.

4. The method of claim 1 , wherein said isomerization conditions include a temperature from 100° C. to 400° C., a molar ratio of hydrocarbon to hydrogen of 1:16 to 1:4, a pressure from about 1 to 10 psi, and a WHSV from 1 to 10 h −1 .

5. A method for the isomerization of a hydrocarbon comprising the step of: contacting a feed stream including a hydrocarbon under isomerization conditions with a composition, said composition including a plurality of nanostructures selected from the group consisting of carbon nanotubes, carbide nanorods, and mixtures thereof, each having a substantially uniform diameter between 1 nm and 100 nm and a length to diameter ratio greater than 5, said nanostructures further including a metal carbide selected from the group consisting of carbides and oxycarbides of a transition metal, rare earth metal or actinide, said nanotubes having been modified by an acidification treatment.

6. The method of claim 5 , wherein said hydrocarbon is selected from the group consisting of normal, branched, and cyclic hydrocarbons.

7. The method of claim 5 , wherein said hydrocarbon is an alkene.

8. The method of claim 5 , wherein said isomerization conditions include a temperature from 100° C. to 400° C., a molar ratio of hydrocarbon to hydrogen of 1:16 to 1:4, a pressure from about 1 to 10 psi, and a WHSV from 1 to 10 h −1 .

9. The method of claim 5 , wherein said acidification treatment is treatment with an acidifying compound.

10. The method of claim 9 , wherein said acidification treatment is selected from the group consisting of halogenation, chlorination, nitrogenation, oxygenation, and phosphorylation.

11. A method for the isomerization of a hydrocarbon comprising the step of: contacting a feed stream including a hydrocarbon under isomerization conditions with a composition, said composition including: (a) a rigid porous structure formed from a plurality of nanostructures selected from the group consisting of carbon nanotubes, carbide nanorods, and mixtures thereof, each having a substantially uniform diameter between 1 nm and 100 nm and a length to diameter ratio greater than 5, said nanostructures further including a metal carbide selected from the group consisting of carbides and oxycarbides of a transition metal, rare earth metal or actinide, said rigid porous structure including a plurality of interstitial spaces between said nanostructures; and (b) a solid acid in said interstitial spaces.

12. The method of claim 11 , wherein said hydrocarbon is selected from the group consisting of normal, branched, and cyclic hydrocarbons.

13. The method of claim 11 , wherein said hydrocarbon is an alkene.

14. The method of claim 11 , wherein said isomerization conditions include a temperature from 100° C. to 400° C., a molar ratio of hydrocarbon to hydrogen of 1:16 to 1:4, a pressure from about 1 to 10 psi, and a WHSV from 1 to 10 h −1 .

15. The method of claim 11 , wherein said solid acid is a compound containing an element selected from the group consisting of aluminum and zirconium.

16. The method of claim 15 , wherein said solid acid is a compound containing aluminum and the solid acid has been chlorinated, sulfated, or phosphated.

17. The method of claim 15 , wherein said solid acid is a compound containing zirconium and the solid acid has been chlorinated, sulfated, or phosphated.

18. The method of claim 11 , wherein said rigid porous structure has a density greater than about 0.5 gm/cm 3 and a porosity greater than about 0.8 cc/gm.

19. The method of claim 18 , wherein said rigid porous structure is substantially free of micropores and has a crush strength greater than about 1 lb/in 2 .

Assignments (3)
RELEASE OF SECURITY INTEREST Recorded Jan 21, 2021
From: WHITE OAK GLOBAL ADVISORS, LLC, AS ADMINISTRATIVE AGENT
To: HYPERION CATALYSIS INTERNATIONAL
Reel/Frame 055058/0494 →
SECURITY AGREEMENT Recorded Sep 17, 2013
From: HYPERION CATALYSIS INTERNATIONAL
To: PDL BIOPHARMA, INC.
Reel/Frame 031227/0086 →
SECURITY AGREEMENT Recorded Aug 16, 2013
From: HYPERION CATALYSIS INTERNATIONAL
To: WHITE OAK GLOBAL ADVISORS, LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 031030/0001 →