IP Library › Granted Patent US 12,516,256
Granted Patent B2
US 12,516,256 · App. 18/214,910 · Granted Jan 6, 2026

Single stage renewable jet production

Inventors: Xiaochun Xu (Annandale, NJ); Alexander J. Dulin (Haddonfield, NJ); Madelyn M. Evans (Annandale, NJ); Richard C. Baliban (Annandale, NJ)
Assignee: EXXONMOBIL TECHNOLOGY AND ENGINEERING COMPANY
C10G67/14C10G3/50C10L1/08C10G2300/1011C10G2300/301C10G2300/304C10G2400/08C10L2200/0469C10L2270/04
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 12,516,256
App. No.
18/214,910
Granted
Jan 6, 2026
Kind
B2
Abstract

Systems and methods are provided for production of renewable jet fuel and/or jet fuel blending component fractions using a single stage reaction system. Although only a single separation stage is used, the systems and methods can reduce or minimize the volume of feedstock that is exposed to hydrocracking conditions while still producing a jet boiling range fraction having beneficial cold flow properties.

Claims (19)

1 . A method for producing a renewable jet boiling range fraction, comprising: contacting a bio-derived feedstock and a hydrocracked, dewaxed co-feed with a hydrotreatment catalyst under effective hydrotreatment conditions to produce a deoxygenated effluent comprising a deoxygenated liquid fraction; separating the deoxygenated liquid fraction to form at least i) a jet boiling range fraction having a T90 distillation point of 230° C. or lower and a freeze point of −40° C. or lower and ii) a second fraction having a final boiling point of 300° C. or higher; contacting at least a portion of the second fraction with a hydrocracking catalyst under hydrocracking conditions to produce a hydrocracked effluent; and cascading at least a portion of the hydrocracked effluent into a reactor containing a dewaxing catalyst under dewaxing conditions to produce an effluent comprising a portion of the hydrocracked, dewaxed co-feed.

2 . The method of claim 1 , wherein the jet boiling range fraction comprises a flash point of 38° C. or higher.

3 . The method of claim 1 , wherein the jet boiling range fraction comprises 1.0 wppm or less of oxygen.

4 . The method of claim 1 , wherein a yield of the jet boiling range fraction is 25 wt % to 45 wt % relative to a weight of the bio-derived feedstock.

5 . The method of claim 1 , wherein the hydrocracking catalyst comprises a zeotype framework structure having a largest pore channel comprising a 12-member ring and wherein the dewaxing catalyst comprises a zeotype framework structure having a largest pore channel comprising a 10-member ring.

6 . The method of claim 1 , wherein the jet boiling range fraction comprises 10 wt % or more of n-paraffins, relative to a weight of the jet boiling range fraction.

7 . The method of claim 1 , the method further comprising: separating at least a portion of the deoxygenated effluent to form a fraction comprising hydrogen and the deoxygenated liquid fraction; and separating at least a portion of the fraction comprising hydrogen to form a recycle fraction containing hydrogen, wherein contacting the bio-derived feedstock and the hydrocracked, dewaxed co-feed with a hydrotreatment catalyst under effective hydrotreatment conditions contacting the bio-derived feedstock and the hydrocracked, dewaxed co-feed in the presence of at least a portion of the recycle fraction.

8 . A method for producing a renewable jet boiling range fraction, comprising: contacting a bio-derived feedstock and a hydrocracked, dewaxed co-feed with a hydrotreatment catalyst under effective hydrotreatment conditions to produce a deoxygenated effluent comprising a deoxygenated liquid fraction; separating, in a separation stage, the deoxygenated liquid fraction to form at least i) a jet boiling range fraction having a T90 distillation point of 230° C. or lower and a freeze point of −40° C. or lower and ii) a second fraction having a final boiling point of 300° C. or higher; contacting at least a portion of the second fraction with a hydrocracking catalyst under hydrocracking conditions to produce a hydrocracked effluent; and cascading at least a portion of the hydrocracked effluent into a reactor containing a dewaxing catalyst under dewaxing conditions to produce an effluent comprising a portion of the hydrocracked, dewaxed co-feed, wherein the separation stage is the is the only separation stage used to produce the renewable jet boiling range fuel from the bio-derived feedstock.

9 . The method of claim 8 , wherein the jet boiling range fraction comprises a flash point of 38° C. or higher.

10 . The method of claim 8 , wherein the jet boiling range fraction comprises 1.0 wppm or less of oxygen.

11 . The method of claim 8 , wherein a yield of the jet boiling range fraction is 25 wt % to 45 wt % relative to a weight of the bio-derived feedstock.

12 . The method of claim 8 , wherein the hydrocracking catalyst comprises a zeotype framework structure having a largest pore channel comprising a 12-member ring and wherein the dewaxing catalyst comprises a zeotype framework structure having a largest pore channel comprising a 10-member ring.

13 . The method of claim 8 , wherein the jet boiling range fraction comprises 10 wt % or more of n-paraffins, relative to a weight of the jet boiling range fraction.

14 . The method of claim 8 , wherein the dewaxing catalyst comprises a binder having a binder surface area of 100 m 2 /g or less, or wherein the dewaxing catalyst comprises a non-noble hydrogenation metal, or a combination thereof.

15 . A method for producing a renewable jet boiling range fraction, comprising: contacting a bio-derived feedstock and a hydrocracked, dewaxed co-feed with a hydrotreatment catalyst under effective hydrotreatment conditions to produce a deoxygenated effluent comprising a deoxygenated liquid fraction; separating the deoxygenated liquid fraction to form at least i) a jet boiling range fraction having a T90 distillation point of 230° C. or lower and a freeze point of −40° C. or lower and ii) a second fraction having a final boiling point of 300° C. or higher; contacting at least a portion of the second fraction with a hydrocracking catalyst under hydrocracking conditions to produce a hydrocracked effluent; and cascading at least a portion of the hydrocracked effluent into a reactor containing a dewaxing catalyst under dewaxing conditions to produce an effluent comprising a portion of the hydrocracked, dewaxed co-feed, wherein the hydrocracking catalyst comprises a noble hydrogenation metal.

16 . The method of claim 15 , wherein the deoxygenated effluent comprises 0.5 wt % or more of H 2 O.

17 . The method of claim 15 , wherein a yield of the jet boiling range fraction is 35 wt % or more relative to a weight of the bio-derived feedstock.

18 . The method of claim 15 , wherein the jet boiling range fraction comprises 5.0 wt % or more of n-paraffins, relative to a weight of the jet boiling range fraction.

19 . The method of claim 15 , the method further comprising: separating at least a portion of the deoxygenated effluent to form a fraction comprising hydrogen and the deoxygenated liquid fraction; and separating at least a portion of the fraction comprising hydrogen to form a recycle fraction containing hydrogen, wherein contacting the bio-derived feedstock and the hydrocracked, dewaxed co-feed with a hydrotreatment catalyst under effective hydrotreatment conditions contacting the bio-derived feedstock and the hydrocracked, dewaxed co-feed in the presence of at least a portion of the recycle fraction.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2023
From: XU, XIAOCHUN; DULIN, ALEXANDER J.; EVANS, MADELYN M.; BALIBAN, RICHARD C.
To: EXXONMOBIL TECHNOLOGY AND ENGINEERING COMPANY
Reel/Frame 064086/0620 →
Continuity (2)
Provisional Application 63356810 · Jun 29, 2022
Related Publication 20240002737A1 · Jan 4, 2024
References Cited (33)
US 5151371A · Quimby et al. · 1992 [cited by applicant]
US 6759438B2 · Rainis et al. · 2004 [cited by applicant]
US 7846323B2 · Abhari et al. · 2010 [cited by applicant]
US 8193399B2 · Gosling · 2012 [cited by examiner]
US 8304591B2 · Aulich et al. · 2012 [cited by applicant]
US 8314274B2 · Marker et al. · 2012 [cited by applicant]
US 8431756B2 · Roberts et al. · 2013 [cited by applicant]
US 8523959B2 · O'Rear · 2013 [cited by applicant]
US 8674160B2 · Hanks et al. · 2014 [cited by applicant]
US 8729330B2 · Hanks et al. · 2014 [cited by applicant]
US 8742183B2 · Mccall et al. · 2014 [cited by applicant]
US 9617479B2 · Fingland et al. · 2017 [cited by applicant]
US 10000712B2 · Novak et al. · 2018 [cited by applicant]
US 10053639B2 · Shih et al. · 2018 [cited by applicant]
US 12139673B2 · Andersson · 2024 [cited by examiner]
US 20080066374A1 · Herskowitz · 2008 [cited by applicant]
US 20090301930A1 · Brandvold et al. · 2009 [cited by applicant]
US 20120209041A1 · Hanks · 2012 [cited by examiner]
US 20160122664A1 · Thakkar · 2016 [cited by applicant]
US 20210371761A1 · Andersson · 2021 [cited by examiner]
US 20220364001A1 · Campani · 2022 [cited by examiner]
US 20230250348A1 · Xu · 2023 [cited by examiner]
US 20230357652A1 · Sala · 2023 [cited by examiner]
US 20230416619A1 · Xu · 2023 [cited by examiner]
US 20250084330A1 · Berkhous · 2025 [cited by examiner]
US 20250154415A1 · Bandy, III · 2025 [cited by examiner]
WO 2020083994A1 · 2020 [cited by applicant]
WO 2021094657A1 · 2021 [cited by applicant]
WO 2021099343A1 · 2021 [cited by applicant]
WO 2021180805A1 · 2021 [cited by applicant]
WO 2021260158A1 · 2021 [cited by applicant]
Ch. Baerlocher et al., “Atlas of Zeolite Frameworks” published on behalf of the Structure Commission of the International Zeolite Association, 6th revised edition, 2007, 405 pages. [cited by applicant]
International Search Report and Written Opinion received for PCT Patent Application No. PCT/US2023/026283, mailed on Oct. 9, 2023, 163 pages. [cited by applicant]