IP Library Granted Patent US 9,415,384
Granted Patent B2
US 9,415,384 · App. 14/409,560 · Granted Aug 16, 2016

Resid hydrotreating catalyst containing titania

Inventors: Rong He (Palo Alto, CA); Stanislaw Plecha (Columbia, MD); Meenakshi S. Krishnamoorthy (Columbia, MD); Bharat M. Patel (Catonsville, MD)
Assignee: Advanced Refining Technologies LLC
B01J37/16B01J21/04B01J21/063B01J23/755B01J23/883B01J27/19B01J35/1019B01J35/1042B01J35/1047B01J35/1071B01J35/1076B01J37/0009B01J37/0045B01J37/03B01J37/12B01J37/28C10G45/00C10G45/08C10G2300/107C10G2300/1077C10G2300/70C10G2300/708
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 9,415,384
App. No.
14/409,560
Granted
Aug 16, 2016
Kind
B2
Abstract

Improved catalyst supports, supported catalyst, and method of preparing and using the catalysts for the hydrodesulfurization of a residuum hydrocarbon feedstock are disclosed. The catalyst supports comprise titania alumina having 5 wt % or less titania and have greater than 70% of their pore volume in pores having a diameter between 70 and 130 and less than 2% in pores having a diameter above 1000. Catalysts prepared from the supports contain Groups 6, 9 and 10 metals or metal compounds, and optionally phosphorus, supported on the titania alumina supports. Catalysts in accordance with the invention exhibit improved sulfur and MCR conversion in hydrotreating processes.

Claims (22)

1. A catalyst support comprising a titania alumina extrudate formed from a peptized co-precipitated titania alumina powder having 5 wt % or less titania based on the total weight of the titania alumina, said support having a total pore volume in the range of from about 0.5 to about 1.0 cubic centimeters per gram, at least 70% of the total pore volume in pores having a diameter between about 70 Å and about 130 Å, less than 5% of the total pore volume have pores in a diameter above 300 Å, as determined by nitrogen porosimetry, and less than 2% of the total pore volume in pores having a diameter above 1000 Å, as determined by mercury penetration porosimetry.

2. The support of claim 1 wherein the amount of titania present in the titania alumina is an amount less than 5 wt %, based on the total weight of the titania alumina.

3. The support of claim 2 wherein the amount of titania present in the titania alumina is an amount from about 0.3 to about 4.5 wt % titania, based on the total weight of the titania alumina.

4. The support of claim 1 wherein the support comprises at least 90 wt % co-precipitated titania alumina.

5. The support of claim 1 wherein: (a) at least 79% of the total pore volume is in pores having a diameter between about 70 Å and about 130 Å; or (b) from about 0.40% to about 1.5% of the total pore volume is in pores having a diameter above 1000 Å; or both (a) and (b).

6. A method for preparing a catalyst for hydrodesulfurization of residuum hydrocarbon feedstocks which method comprises: impregnating the porous extruded support of claim 1 with an aqueous solution comprising at least one catalytic agent or catalytic agent precursor selected from the group consisting of a compound of Group 6 metals of The Periodic Table, Group 9 metals of the Periodic Table, Group 10 metals of The Periodic Table, and combinations thereof, and optionally phosphorous, said compounds being thermally decomposable to their corresponding metal oxides, and thereafter drying and calcining the resulting impregnated support to provide a supported catalyst.

7. A catalyst produced by the method according to claim 6 .

8. A catalyst suitable for use in hydrodesulfurization of residuum hydrocarbon feedstocks comprising:

(a) a support comprising a titania alumina extrudate formed from a peptized co-precipitated titania alumina powder having 5 wt % or less titania based on the total weight of the titania alumina; and

(b) at least one catalytic agent comprising a metal selected from the group consisting of a Group 6 metal of The Periodic Table, a Group 9 metal of The Periodic Table, a Group 10 metal of The Periodic Table, and combinations thereof, and optionally phosphorous;

wherein the support is characterized as having:

(i) a total pore volume of from about 0.5 to about 1.0 cubic centimeters per gram;

(ii) at least 70% of the total pore volume in pores having a diameter between about 70 Å and about 130 Å;

(iii) less than 5% of the total pore volume in pores having a diameter above 300 Å, as determined by nitrogen porosimetry; and

(iv) less than 2% of the total pore volume in pores having a diameter above 1000 Å, as determined by mercury penetration porosimetry.

9. The catalyst of claim 8 wherein the calcined support comprises at least 90 wt % of the co-precipitated titania alumina.

10. The catalyst of claim 8 wherein the amount of titania present in the co-precipitated titania alumina is an amount less than 5 wt %, based on the total weight of the titania alumina.

11. The catalyst of claim 10 wherein the amount of titania present in the co-precipitated titania alumina is an amount from about 0.3 to about 4.5 wt % titania, based on the total weight of the titania alumina.

12. The catalyst of claim 8 wherein: (a) at least 79% of the total pore volume of the support is in pores having a diameter between about 70 Å and about 130 Å; or (b) from about 0.40% to about 1.5% of the total pore volume is in pores having a diameter above 1000 Å; or both (a) and (b).

13. The catalyst of claim 8 wherein said at least one catalytic agent comprises a metal selected from the group consisting of cobalt, nickel, molybdenum, and combinations thereof, and optionally phosphorous.

14. A process for hydrotreating residuum hydrocarbon feedstocks comprising at least one of sulfur or microcarbon residue (MCR), which process comprises contacting said residuum feedstocks with a catalyst of claim 8 under hydrodesulfurization process conditions and producing a hydrotreated residuum hydrocarbon fraction having a reduced sulfur content or a reduced MCR content or both a reduced sulfur and a reduced MCR content compared to the residuum hydrocarbon feedstock.

15. The process of claim 14 wherein the residuum hydrocarbon feedstock is contacted with the catalyst at a reaction temperature from about 300° C. to about 450° C., a hydrogen pressure of about 120 bar to about 200 bar, a H 2 :oil ratio ranging from about 250 Nl/l to about 1400 N1/1, and a space velocity from about 0.2 hr −1 to about 2.0 hr −1 .

Assignments (7)
RELEASE OF SECURITY INTEREST SUPPLEMENT NO. 3 Recorded Feb 2, 2026
From: WILMINGTON TRUST, NATIONAL ASSOCIATION
To: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
Reel/Frame 074612/0540 →
NOTES SECURITY INTEREST Recorded Jan 29, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 074532/0229 →
SUPPLEMENT NO. 3 TO PATENT SECURITY AGREEMENT Recorded Jan 23, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 074503/0898 →
SUPPLEMENT NO. 3 TO PATENT SECURITY AGREEMENT Recorded Jan 23, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 074503/0889 →
SUPPLEMENT NO. 1 TO PATENT SECURITY AGREEMENT Recorded Jan 23, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 074503/0861 →
SECURITY INTEREST (SUPPLEMENTAL NO. 3) Recorded Jan 22, 2026
From: W. R. GRACE & CO.-CONN.; ADVANCED REFINING TECHNOLOGIES LLC
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 074475/0514 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 23, 2014
From: HE, RONG; PLECHA, STANISLAW; KRISHNAMOORTHY, MEENAKSHI S.; PATEL, BHARAT M.
To: ADVANCED REFINING TECHNOLOGIES LLC
Reel/Frame 034578/0364 →
Continuity (2)
Provisional Application 61662003 · Jun 20, 2012
Related Publication 20150144532A1 · May 28, 2015