IP Library › Granted Patent US 12,618,016
Granted Patent B2
US 12,618,016 · App. 18/808,193 · Granted May 5, 2026

Methods for producing aviation fuels

Inventors: Thomas J. Malinski (Kingwood, TX); Michael S. Webster-Gardiner (Kingwood, TX); Steven M. Bischof (Kingwood, TX); James L. Hillier (Kingwood, TX); Jeffery C. Gee (Kingwood, TX); Spencer A. Kerns (Kingwood, TX); Reza Khankal (Kingwood, TX); Jared T. Fern (Kingwood, TX)
Assignee: Chevron Phillips Chemical Company LP
C10G69/126C07C2/08C07C6/04C10G2300/1092C10G2300/70C10G2400/08
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Quick Facts
Patent No.
US 12,618,016
App. No.
18/808,193
Granted
May 5, 2026
Kind
B2
Abstract

Processes for making aviation fuels include a step of forming a C 16− olefin stream by oligomerizing a mixture of decenes with a C 6− alpha-olefin or by subjecting the mixture of decenes and a C 8− alpha-olefin to metathesis. The C 16− olefin stream is then hydrogenated to form C 16− paraffins, and these C 16− paraffins can be used to form an aviation fuel. Particular C 11 -C 16 olefin compositions and paraffin compositions prepared by these processes also are described.

Claims (37)

1 . A process for making a C 16 -olefin stream, the process comprising:

(a) contacting an ethylene feed with a first catalyst system comprising a first oligomerization catalyst to form an oligomerization product comprising at least one C 4 -C 8 alpha-olefin and a mixture of decenes;

(b) separating the mixture of decenes from the oligomerization product;

(c) contacting the mixture of decenes with at least one C 6− alpha-olefin in the presence of a second catalyst system comprising a second oligomerization catalyst to provide the C 16− olefin stream;

(d) optionally, hydrogenating the C 16− olefin stream in the presence of a first hydrogenation catalyst to provide C 16− paraffins; and

(e) optionally, blending the C 16− paraffins as a component to form an aviation fuel.

2 . The process of claim 1 , wherein the at least one C 6− alpha-olefin comprises propylene, 1-butene, isobutylene, 1-pentene, 1-hexene, or a combination thereof.

3 . The process of claim 1 , wherein the mixture of decenes comprises 1-decene, 2-butyl-1-hexene, 3-propyl-1-heptene, 4-ethyl-1-octene, 5-methyl-1-nonene, 4-decene, 5-decene, or any combination thereof.

4 . The process of claim 3 , wherein the mixture of decenes comprises from 76 mol % to 95 mol % C 10 monoolefins.

5 . The process of claim 1 , wherein the oligomerization product comprises 1-butene, 1-hexene, 1-octene, dodecenes, tetradecenes, or any combination thereof.

6 . The process of claim 1 , wherein the oligomerization product comprises:

at least 60 mol % 1-hexene, at least 60 mol % 1-octene, or at least 60 mol % 1-hexene and 1-octene combined; or

from 70 wt. % to 99.8 wt. % hexene or from 70 wt. % to 99.8 wt. % octene, and at least 0.2 wt. % of the mixture of decenes.

7 . The process of claim 1 , wherein the first catalyst system, the second catalyst system, or both comprise independently a chromium-based catalyst, a metallocene-based catalyst, a Ziegler-Natta based catalyst, a metal-oxide supported Group 6-10 transition metal-based catalyst, or a combination thereof.

8 . The process of claim 7 , wherein the first catalyst system, the second catalyst system, or both further comprise a metal alkyl compound selected from an organoaluminum compound, an organoaluminoxane, an organoboron compound, an organozinc compound, an organomagnesium compound, an organolithium compound, or any combination thereof.

9 . The process of claim 1 , wherein the first catalyst system, the second catalyst system, or both comprise independently a chromium-based catalyst, and the chromium-based catalyst comprises (a) a chromium-containing compound, (b) a heteroatomic ligand, (c) a metal alkyl compound, and (d) optionally, a diluent.

10 . The process of claim 9 , wherein the heteroatomic ligand is selected from a pyrrole compound, a diphosphino aminyl compound, an N 2 -phosphinyl amidine compound, an N 2 -phosphinyl formamidine compound, or combinations thereof.

11 . The process of claim 10 , wherein the diluent is present and comprises a hydrocarbon, a halogenated hydrocarbon, or combinations thereof.

12 . The process of claim 1 , wherein the first catalyst system, the second catalyst system, or both independently comprise:

(a) molybdenum oxide on alumina (MoO 3 /Al 2 O 3 ), tungsten oxide on silica (WO 3 /SiO 2 ), tungsten oxide on silica-alumina (WO 3 /SiO 2 /Al 2 O 3 ), rhenium oxide on alumina (Re 2 O 7 /Al 2 O 3 ), cobalt oxide and molybdenum oxide on alumina (CoO/MoO 3 /Al 2 O 3 ), rhenium oxide on alumina activated with tetramethyl tin (Re 2 O 7 /Al 2 O 3 /SnMe 4 ), or any combination thereof; or

(b) tungstated zirconium, molybdenum zirconium, nickel and/or cobalt doped tungstated zirconium, nickel and/or cobalt doped molybdenum zirconium catalysts, a Group 3 to Group 12 metal-treated zeolite, or combinations thereof.

13 . The process of claim 1 , wherein the first hydrogenation catalyst comprises:

(a) a heterogeneous catalyst selected from a Group 8-12 metal deposited on a carrier selected from carbon, silica, alumina, silica-alumina, a zeolite, or calcium carbonate; or

(b) a homogeneous catalyst selected from (i) a Ziegler catalyst comprising an organic salt of a Group 6-10 metal and an organoaluminum compound, or (ii) a coordination compound of Ru, Rh, or Ir, or (iii) a Group 4 metal organometallic compound.

14 . The process of claim 1 , wherein the C 16− olefin stream comprises:

(1) 2-methyl-4-butyl-3-octene, 2-methyl-5-propylnon-3-ene, 6-ethyl-2-methyldec-3-ene, and/or 2,7-dimethylundec-3-ene;

(2) 5-butyl-3-methylnon-4-ene, 3-methyl-6-propyldec-4-ene, 7-ethyl-3-methylundec-4-ene, and/or 3,8-dimethyldodec-4-ene;

(3) 2,2-dimethyl-4-butyl-3-octene, 2,2-dimethyl-5-propyl-3-nonene, 2,2-dimethyl-6-ethyl-3-decene, and/or 2,2,7-trimethyl-3-undecene;

(4) 6-butyl-4-methyldec-5-ene, 4-methyl-7-propylundec-5-ene, 8-ethyl-4-methyldodec-5-ene, and/or 4,9-dimethyltridec-5-ene; or

(5) 5-butyl-7-methylundec-5-ene, 5-methyl-8-propyldodec-6-ene, 9-ethyl-5-methyltridec-6-ene, and/or 5,10-dimethyltetradec-6-ene.

15 . The process of claim 1 , wherein:

at least a portion of the ethylene feed is a bio-ethylene feed; and

the aviation fuel is formed and is a sustainable aviation fuel.

16 . The process of claim 15 , wherein:

(a) the sustainable aviation fuel is certified as compliant with the Carbon Offsetting and Reduction Scheme for International Aviation (CORSIA) sustainability criteria in accordance with the International Sustainability and Carbon Certification (ISCC) CORSIA certification system; or

(b) the sustainable aviation fuel is certified as a Lower Carbon Aviation Fuel (LCAF) in accordance with the International Sustainability and Carbon Certification (ISCC) LCAF certification system;

wherein the certification is based upon the weight or fraction of the sustainable aviation fuel attributable to the biomass ethanol determined by mass balance and a free attribution method.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2026
From: KHANKAL, REZA; FERN, JARED T
To: CHEVRON PHILLIPS CHEMICAL COMPANY LP
Reel/Frame 074080/0519 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2024
From: MALINSKI, THOMAS J.; WEBSTER-GARDINER, MICHAEL S.; BISCHOF, STEVEN M.; HILLIER, JAMES L.; GEE, JEFFERY C.; KERNS, SPENCER A.
To: CHEVRON PHILLIPS CHEMICAL COMPANY LP
Reel/Frame 068915/0027 →
Continuity (3)
Continuation In Part 18462558 · Sep 7, 2023
Continuation In Part 18462567 · Sep 7, 2023
Related Publication 20260049256A1 · Feb 19, 2026
References Cited (81)
US 2882244A · Milton · 1959 [cited by applicant]
US 3130007A · Breck · 1964 [cited by applicant]
US 3216789A · Breck · 1965 [cited by applicant]
US 4021447A · Rubin · 1977 [cited by applicant]
US 4503023A · Breck · 1985 [cited by applicant]
US 6190539B1 · Holtermann · 2001 [cited by applicant]
US 6291733B1 · Small · 2001 [cited by applicant]
US 6812180B2 · Fukunaga · 2004 [cited by applicant]
US 6914165B2 · Flego · 2005 [cited by applicant]
US 7153801B2 · Wu · 2006 [cited by applicant]
US 7902105B2 · Khare · 2011 [cited by applicant]
US 8334420B2 · Small · 2012 [cited by applicant]
US 8680003B2 · Sydora · 2014 [cited by applicant]
US 8791217B2 · Hlavinka · 2014 [cited by applicant]
US 8969640B2 · Blommel · 2015 [cited by applicant]
US 9115225B2 · Hlavinka · 2015 [cited by applicant]
US 9175109B1 · Kreischer · 2015 [cited by applicant]
US 9352309B2 · Sydora · 2016 [cited by applicant]
US 9567541B2 · Frey · 2017 [cited by applicant]
US 9708549B2 · Gee · 2017 [cited by applicant]
US 9745230B2 · Small · 2017 [cited by applicant]
US 9862655B2 · Fichtl · 2018 [cited by applicant]
US 9879192B2 · Watermeyer De Wet · 2018 [cited by applicant]
US 9914672B2 · Greene · 2018 [cited by applicant]
US 9957449B2 · Luebke · 2018 [cited by applicant]
US 9968921B2 · Kilgore · 2018 [cited by applicant]
US 10113130B1 · Harvey · 2018 [cited by applicant]
US 10183899B2 · Bischof · 2019 [cited by applicant]
US 10240102B2 · Small · 2019 [cited by applicant]
US 10329212B2 · Fern · 2019 [cited by applicant]
US 10414698B2 · Fern · 2019 [cited by applicant]
US 10435334B2 · Bischof · 2019 [cited by applicant]
US 10435336B2 · Kreischer · 2019 [cited by applicant]
US 10544070B2 · Small · 2020 [cited by applicant]
US 10577291B2 · Frey · 2020 [cited by applicant]
US 10647626B2 · Coffin · 2020 [cited by applicant]
US 10647931B2 · Pucci · 2020 [cited by applicant]
US 10793781B2 · Hakola · 2020 [cited by applicant]
US 10920151B2 · Brandvold · 2021 [cited by applicant]
US 10927052B2 · Coffin · 2021 [cited by applicant]
US 11072569B2 · Bischof · 2021 [cited by applicant]
US 11078433B2 · Smith · 2021 [cited by applicant]
US 11174205B2 · Gee · 2021 [cited by applicant]
US 11186530B2 · Gee · 2021 [cited by applicant]
US 11312671B2 · Barias · 2022 [cited by applicant]
US 11358914B2 · Bischof · 2022 [cited by applicant]
US 11639320B1 · Chang · 2023 [cited by applicant]
US 20090158637A1 · Mccall · 2009 [cited by applicant]
US 20090250376A1 · Brandvold · 2009 [cited by applicant]
US 20120197053A1 · Cantrell · 2012 [cited by examiner]
US 20120209045A1 · Wright · 2012 [cited by applicant]
US 20140051898A1 · Wright · 2014 [cited by applicant]
US 20160194257A1 · Lilga · 2016 [cited by examiner]
US 20180016204A1 · Coffin · 2018 [cited by examiner]
US 20180065115A1 · Alvez-Manoli · 2018 [cited by applicant]
US 20210009911A1 · Medoff · 2021 [cited by applicant]
US 20210355047A1 · Li · 2021 [cited by applicant]
US 20220396534A1 · Vincent · 2022 [cited by applicant]
US 20220396741A1 · Vincent · 2022 [cited by applicant]
US 20230313048A1 · Jan · 2023 [cited by examiner]
US 20240246887A1 · Mathur · 2024 [cited by applicant]
WO 2002004575A2 · 2002 [cited by applicant]
WO 2018071905A1 · 2018 [cited by applicant]
WO 2026027733A1 · 2026 [cited by applicant]
WO 2026027734A1 · 2026 [cited by applicant]
WO 2026027735A1 · 2026 [cited by applicant]
WO 2026027736A1 · 2026 [cited by applicant]
Non-Final Office Action issued in U.S. Appl. No. 18/462,567, filed Sep. 7, 2023. Notification issued Mar. 20, 2025, 21 pages. [cited by applicant]
Sustainable Aviation Fuel: Review of Technical Pathways, U.S. Department of Energy, energy.gov/eere/bioenergy, 2020, 81 pages. [cited by applicant]
Toxicological Profile for Jet Fuels JP-4 and JP-7, U.S. Department of Health and Human Services, Agency for Toxic Substances and Disease Registry, Jun. 1995, 150 pages. [cited by applicant]
Babu B Hari et al: “An integrated process for production of jet-fuel range olefins from ethylene using Ni-AISBA-15 and Amberlyst-35 catalysts”, Applied Catalysis A: General, vol. 530, 2017, pp. 48-55. [cited by applicant]
Faroon et al., Toxicological Profile for Jet Fuels JP-4 and JP-7, U.S. Department of Health and Human Services. Agency for Toxic Substances and Disease Registry, Jun. 1995, 150 pages. [cited by applicant]
Holladay et al., Sustainable Aviation Fuel: Review of Technical Pathways, US Dept of Energy, Office of Energy Efficiency and Renewable Energy, Sep. 2020, 81 pages. [cited by applicant]
International Search Report and Written Opinion issued in corresponding PCT Application No. PCT/US2024/045290, mailed on Dec. 20, 2024, 16 pages. [cited by applicant]
ISCC Certification for Sustainable Aviation Fuels, ISSC System GmbH, 19 pages. [cited by applicant]
International Search Report and Written Opinion issued in corresponding PCT Application No. PCT/US2024/045299, mailed on Feb. 3, 2025, 24 pages. [cited by applicant]
Small, B., Insights on the Mechanism for Ethylene Tetramerization, Organometamcs, DOI: 10.1021/acs.organomet.2c00285, Jun. 2022, 12 pages. [cited by applicant]
Axens Oligomerization—Bio-Olefin Upgrading, Axens Renewable Paythways, 1 page. [cited by applicant]
International Search Report and Written Opinion issued in corresponding PCT Application No. PCT/US2025/042160, mailed on Nov. 21, 2025, 13 pp. [cited by applicant]
Liu et al., “Experimental and numberical analysis on flow characteristics and pyrolysis mechanism of hydrocarbon fuel with a novel online hybred method,” ScienceDirect, Energy Conversion and Management, 198 (2019) 11181… [cited by applicant]
Gao et al.,“Novel measurement of isobaric specific heat capacity for kerosene RP-3 at high temperature and high pressure,” ScienceDirect, Thermochimica Acta 638 (2016) pp. 113-119. [cited by applicant]