IP Library Granted Patent US 9,328,039
Granted Patent B2
US 9,328,039 · App. 13/812,707 · Granted May 3, 2016

Process for selective hydrogenation in the presence of a catalyst based on a metal from group VIII prepared using at least one cyclic oligosaccharide

Inventors: Fabrice Diehl (Lyons, FR); Anne Claire Dubreuil (Lyons, FR); Josselin Janvier (Nanterre, FR); Cecile Thomazeau (Lyons, FR)
Assignee: IFP ENERGIES NOUVELLES
C07C5/02B01J23/755B01J33/00B01J37/0203B01J37/0205B01J37/20C07C7/167C10G45/34C10G45/36C10G45/52C10G69/06B01J21/04B01J23/40B01J23/74C07C2523/755C10G2300/1011C10G2300/301C10G2300/4018C10G2400/20C10G2400/22Y02P20/52
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Quick Facts
Patent No.
US 9,328,039
App. No.
13/812,707
Granted
May 3, 2016
Kind
B2
Abstract

Selective hydrogenation of a polyunsaturated hydrocarbon feed containing at least 2 carbon atoms per molecule and having an end point of 250° C. or less, by contacting said feed with a catalyst having an active phase of at least one metal from group VIII deposited on a support formed by at least one oxide, said catalyst being prepared using a process involving at least: i) contacting said support with at least one solution containing at least one precursor of metal from group VIII; ii) contacting said support with at least one organic compound formed from at least one cyclic oligosaccharide composed of at least 6 α-(1,4)-bonded glucopyranose subunits; iii) calcining to obtain metal from group VIII in oxide form; i) and ii) possibly being carried out separately, in any order, or simultaneously.

Claims (18)

1. A process for the selective hydrogenation of a hydrocarbon feed comprising at least 2 carbon atoms per molecule and having an end boiling point of 250° C. or less, said hydrocarbon feed comprising acetylenes, diolefins or a mixture thereof, said process comprising bringing said feed into contact with at least one catalyst the active phase of which comprises at least one metal from group VIII deposited on a support formed by at least one oxide, said catalyst being prepared using a process comprising at least:

i) at least once contacting said support with at least one solution containing at least one precursor of at least said metal from group VIII;

ii) at least once contacting at least said support with at least one organic compound formed from at least one cyclic oligosaccharide having at least 6 α-(1,4)-bonded glucopyranose subunits;

iii) calcining at least once to obtain at least said metal from said group VIII in the oxide form;

i) and ii) being carried out separately, in any order, or simultaneously.

2. The selective hydrogenation process according to claim 1 , in which said hydrocarbon feed is a C2 steam cracked cut, a C3 steam cracked cut, a C4 steam cracked cut, a C5 steam cracked cut or a steam cracked gasoline.

3. The selective hydrogenation process according to claim 2 , in which said hydrocarbon feed is a steam cracked gasoline.

4. The selective hydrogenation process according to claim 3 , carried out at a temperature of 20° C. to 200° C., at a pressure of 0.4 to 5 MPa and at an hourly space velocity (defined as the ratio of the volume flow rate of feed to the volume of catalyst) of 0.2 to 30 h −1 .

5. The selective hydrogenation process according to claim 1 , in which said metal from group VIII present in the active phase is nickel.

6. The selective hydrogenation process according to claim 1 , in which said active phase comprises at least one additional metal from group VIII or group IB.

7. The selective hydrogenation process according to claim 1 , in which said support comprises an alumina, silicas or silica alumina.

8. The selective hydrogenation process according to claim 1 , in which said organic compound is a cyclodextrin, substituted cyclodextrin, polymerized cyclodextrin or a mixture of cyclodextrins.

9. The selective hydrogenation process according to claim 8 , in which the cyclodextrin is α-cyclodextrin, β-cyclodextrin and γ-cyclodextrin respectively composed of 6, 7 and 8 α-(1,4)-bonded glucopyranose subunits.

10. The selective hydrogenation process according to claim 8 , in which the substituted cyclodextrins is hydroxypropyl beta-cyclodextrin or methylated beta-cyclodextrins.

11. The selective hydrogenation process according to claim 1 , in which said organic compound for carrying out said step ii) is introduced such that the molar ratio {(metal(s) from group VIII in the oxide form present in the active phase of the catalyst obtained from said step iii)/organic compound} is 10 to 300.

12. The selective hydrogenation process according to claim 1 , in which i) and ii) are carried out simultaneously a plurality of times.

13. The selective hydrogenation process according to claim 1 , in which ii) is carried out prior to i).

14. The selective hydrogenation process according to claim 1 in which, when the active phase of the catalyst comprises nickel as the metal from group VIII, said catalyst is prepared in accordance with a process comprising at least v) passivating said catalyst using at least one sulphur-containing compound.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2013
From: DIEHL, FABRICE; DUBREUIL, ANNE-CLAIRE; JANVIER, JOSSELIN; THOMAZEAU, CECILE
To: IFP ENERGIES NOUVELLES
Reel/Frame 029837/0070 →
Priority Claims (1)
FR 10 03189 · Jul 29, 2010 · national
Continuity (1)
Related Publication 20130150639A1 · Jun 13, 2013