Patent · US12391891B2 · B2 · US
Natural gas liquids upgrading process: two-step catalytic process for alkane dehydrogenation and oligomerization
- (11) Publication number
- US12391891B2
- (21) Application number
- 18/183,377
- (22) Filing date
- 2023-03-14
- (30) Priority date
- 2017-09-07
- (43) Publication date
- 2025-08-19
- (45) Date of grant
- 2025-08-19
- (51) IPC
- B01J 21/02; B01J 29/46; B25J 9/16; C10G 59/02; G06T 15/20; G06T 19/20; G06T 7/73
- (52) CPC
- C10G Cracking hydrocarbon oils; production of liquid hydrocarbon mixtures, e.g. by destructive hydrogenation, oligomerisation, polymerisation; recovery of hydrocarbon oils from oil-shale, oil-sand, or gases; refining mixtures mainly consisting of hydrocarbons; reforming of naphtha; mineral waxes: 59/02, 11/02, 11/04, 50/00, 57/02
- B01J Chemical or physical processes, e.g. catalysis or colloid chemistry; their relevant apparatus: 21/02, 29/46
- B25J Manipulators; chambers provided with manipulation devices: 9/1697
- G06T Image data processing or generation, in general: 15/20, 19/20, 2207/20081, 2207/20084, 2219/2016, 7/73
- (73) Assignee
- Purdue Research Foundation
- (72) Inventors
- Rakesh Agrawal; Jeffrey J. Siirola; Taufik Ridha; Yiru Li; Fabio H. Ribeiro; Jeffrey T. Miller
- (54) Title
- Natural gas liquids upgrading process: two-step catalytic process for alkane dehydrogenation and oligomerization
- (57) Abstract
A process to catalytically transform natural gas liquid (NGL) into higher molecular weight hydrocarbons includes providing an NGL stream, catalytically dehydrogenating at least a portion of the NGL stream components to their corresponding alkene derivatives, catalytically oligomerizing at least a portion of the alkenes to higher molecular weight hydrocarbons and recovering the higher molecular weight hydrocarbons. The NGL stream can be extracted from a gas stream such as a gas stream coming from shale formations. The higher molecular weight hydrocarbons can be hydrocarbons that are liquid at ambient temperature and ambient pressure.
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Claims (19)
- A non-oxidative process for catalytically transforming a natural gas liquid (NGL) into one or more higher molecular weight hydrocarbons, comprising: providing a hydrocarbon containing gas stream comprising C 4 alkanes; catalytically dehydrogenating at least a portion of the hydrocarbon containing gas stream to corresponding alkene derivatives using at least one bimetallic catalyst, providing an effluent comprising unreacted C 4 alkanes, C 4 alkenes and hydrogen; catalytically oligomerizing at least a portion of the C 4 alkenes in the effluent to provide one or more higher molecular weight hydrocarbons; and recovering the higher molecular weight hydrocarbons, wherein the at least one bimetallic catalyst is a zero valent metallic alloy that comprises a combination of a first metal chosen from the group consisting of platinum and palladium, and a second metal chosen from the group consisting of zinc, manganese, vanadium, chromium and combinations thereof, and a support.
- The process of claim 1, wherein the hydrocarbon containing gas stream is derived from a shale formation.
- The process of claim 1, further comprising recycling the unreacted C 4 alkanes and C 4 alkenes after the catalytic oligomerization reaction.
- The process of claim 1, wherein the first metal is Pt, and the second metal is chosen from the group consisting of Zn, Mn, V, and Cr.
- The process of claim 1, wherein the at least one bimetallic catalyst is chosen from the group consisting of PtZn, PdZn, PtMn, PtCr, PtV, and PdMn.
- The process of claim 1, wherein the at least one bimetallic catalyst comprises a support of refractory oxide chosen from the group consisting of silica, alumina, silica-alumina, titania, magnesium oxide, zeolites, aluminophosphates and combinations thereof.
- The process of claim 1, further comprising removing the hydrogen after catalytic dehydrogenation; and utilizing the removed hydrogen to increase saturation and reduce the alkene content of the higher molecular weight hydrocarbon stream.
- The process of claim 1, wherein the at least one bimetallic catalyst comprises a support of refractory oxide chosen from the group consisting of silica, alumina, and zeolites.
- The process of claim 1, wherein the hydrocarbon containing gas stream comprising C 4 alkanes contains no isobutane.
- A non-oxidative process for catalytically transforming a natural gas liquid (NGL) into one or more higher molecular weight hydrocarbons, comprising: providing a hydrocarbon containing gas stream consisting of C 2 to C 4 alkanes; catalytically dehydrogenating at least a portion of the hydrocarbon containing gas stream to corresponding alkene derivatives and hydrogen using at least one bimetallic catalyst, providing an effluent consisting of unreacted C 2 -C 4 alkanes, C 2 -C 4 alkenes and hydrogen; catalytically oligomerizing at least a portion of the C 2 -C 4 alkenes in the presence of at least one oligomerization catalyst to provide one or more higher molecular weight hydrocarbons; and recovering the higher molecular weight hydrocarbons, wherein the at least one oligomerization catalyst comprises H-ZSM-5, B - Al - H-ZSM-5, or a combination thereof, and wherein the at least one bimetallic catalyst is a zero valent metallic alloy that comprises a combination of a first metal chosen from the group consisting of platinum and palladium, and a second metal chosen from the group consisting of manganese, vanadium, chromium and combinations thereof, and a support.
- The process of claim 10, wherein the hydrocarbon containing gas stream is derived from a shale formation.
- The process of claim 10, wherein the hydrocarbon containing gas stream consisting of C 2 to C 4 alkanes contains no isobutane.
- A process for catalytically transforming a natural gas liquid (NGL) into one or more higher molecular weight hydrocarbons, comprising: providing a hydrocarbon containing gas stream that is derived from a shale formation, the hydrocarbon containing gas stream comprising one or more light alkanes chosen from the group consisting of C 2, C 3, and C 4 alkanes; catalytically dehydrogenating at least a portion of the light alkanes to corresponding alkene derivatives; catalytically oligomerizing at least a portion of the alkenes in the presence of at least one oligomerization catalyst to provide one or more higher molecular weight hydrocarbons; and recovering the higher molecular weight hydrocarbons, wherein the at least one oligomerization catalyst comprises: a crystalline microporous zeolite structure having MFI topology, wherein heteroatoms within the zeolite structure are selected from the group consisting of aluminum, gallium, iron and combinations thereof, and wherein trivalent boron atoms within the zeolite structure are substituted for tetravalent silicon atoms.
- The process of claim 13, wherein the group consisting of C 2, C 3, and C 4 alkanes contains no isobutane.
- The process of claim 13, wherein the aluminum, gallium or iron are present in an amount from 0.001 wt % to 30 wt % on an elemental basis of the oligomerization catalyst.
- The process of claim 13, wherein the substitution of trivalent boron atoms for tetravalent silicon atoms do not behave as Brønsted acid sites for catalysis.
- The process of claim 13, wherein a Brønsted acid site that compensate framework boron atoms have low activity compared to those that compensate framework aluminum or gallium or iron atoms.
- The process of claim 13, wherein a Brønsted acid site that compensate framework boron atoms are significantly weaker acid sites compared to those that compensate framework aluminum or gallium or iron atoms.
- The process of claim 13, wherein the boron is present in an amount ranging from 0.001 wt % to 10 wt % on an elemental basis of the oligomerization catalyst.
Description
The present disclosure is directed to new hydrocarbon upgrading processes that include the dehydrogenation of light alkanes to their respective alkene derivatives, commonly known as olefins, followed by oligomerization of the light olefins to higher molecular weight hydrocarbon derivatives. The longer chain higher molecular weight hydrocarbons have a greater value than the lighter alkanes.
More efficient utilization of petroleum and gas reserves is an important strategy for the deployment of future energy generation. Shale gas has become an increasingly important source of natural gas in the United States, and the U.S. government's Energy Information Administration predicts that by 2040, seventy percent of the United States' natural gas supply will come from shale gas. Many of these shale gas formations contain wet gases, which can include substantial concentrations of natural gas liquids (NGL). NGL is a mixture of hydrocarbons made up primarily of ethane (C 2), propane (C 3), butane (C 4), and pentane (C 5). Several major shale gas formations such as Marcellus and Bakken are located far away from historically gas producing and processing region such as the Gulf Coast. These resources can be considered as stranded gas. Also, associated gas, which is a byproduct of shale oil production and may contain substantial concentration of NGL, is generally flared, vented, or injected back to the shale oil reservoir at high cost. Construction of pipelines to transport natural gas liquids to large existing processing plant complexes, such as the Gulf Coast, can be capital intensive.
Citations (16)
- US4656016A
- US4751341A
- US5258564A
- WO1993016020A2
- US5264643A
- US6492548B1
- US20060102468A1
- US20110282120A1
- US20120271085A1
- US20150158786A1
- US20140256892A1
- US20150159099A1
- US20150157998A1
- US20160237004A1
- US20180170838A1
- US11603500B2
Record as JSON
{
"publication_number": "US12391891B2",
"country": "US",
"kind": "B2",
"title": "Natural gas liquids upgrading process: two-step catalytic process for alkane dehydrogenation and oligomerization",
"abstract": "A process to catalytically transform natural gas liquid (NGL) into higher molecular weight hydrocarbons includes providing an NGL stream, catalytically dehydrogenating at least a portion of the NGL stream components to their corresponding alkene derivatives, catalytically oligomerizing at least a portion of the alkenes to higher molecular weight hydrocarbons and recovering the higher molecular weight hydrocarbons. The NGL stream can be extracted from a gas stream such as a gas stream coming from shale formations. The higher molecular weight hydrocarbons can be hydrocarbons that are liquid at ambient temperature and ambient pressure.",
"claims": [
"1. A non-oxidative process for catalytically transforming a natural gas liquid (NGL) into one or more higher molecular weight hydrocarbons, comprising: providing a hydrocarbon containing gas stream comprising C 4 alkanes; catalytically dehydrogenating at least a portion of the hydrocarbon containing gas stream to corresponding alkene derivatives using at least one bimetallic catalyst, providing an effluent comprising unreacted C 4 alkanes, C 4 alkenes and hydrogen; catalytically oligomerizing at least a portion of the C 4 alkenes in the effluent to provide one or more higher molecular weight hydrocarbons; and recovering the higher molecular weight hydrocarbons, wherein the at least one bimetallic catalyst is a zero valent metallic alloy that comprises a combination of a first metal chosen from the group consisting of platinum and palladium, and a second metal chosen from the group consisting of zinc, manganese, vanadium, chromium and combinations thereof, and a support.",
"2. The process of claim 1, wherein the hydrocarbon containing gas stream is derived from a shale formation.",
"3. The process of claim 1, further comprising recycling the unreacted C 4 alkanes and C 4 alkenes after the catalytic oligomerization reaction.",
"4. The process of claim 1, wherein the first metal is Pt, and the second metal is chosen from the group consisting of Zn, Mn, V, and Cr.",
"5. The process of claim 1, wherein the at least one bimetallic catalyst is chosen from the group consisting of PtZn, PdZn, PtMn, PtCr, PtV, and PdMn.",
"6. The process of claim 1, wherein the at least one bimetallic catalyst comprises a support of refractory oxide chosen from the group consisting of silica, alumina, silica-alumina, titania, magnesium oxide, zeolites, aluminophosphates and combinations thereof.",
"7. The process of claim 1, further comprising removing the hydrogen after catalytic dehydrogenation; and utilizing the removed hydrogen to increase saturation and reduce the alkene content of the higher molecular weight hydrocarbon stream.",
"8. The process of claim 1, wherein the at least one bimetallic catalyst comprises a support of refractory oxide chosen from the group consisting of silica, alumina, and zeolites.",
"9. The process of claim 1, wherein the hydrocarbon containing gas stream comprising C 4 alkanes contains no isobutane.",
"10. A non-oxidative process for catalytically transforming a natural gas liquid (NGL) into one or more higher molecular weight hydrocarbons, comprising: providing a hydrocarbon containing gas stream consisting of C 2 to C 4 alkanes; catalytically dehydrogenating at least a portion of the hydrocarbon containing gas stream to corresponding alkene derivatives and hydrogen using at least one bimetallic catalyst, providing an effluent consisting of unreacted C 2 -C 4 alkanes, C 2 -C 4 alkenes and hydrogen; catalytically oligomerizing at least a portion of the C 2 -C 4 alkenes in the presence of at least one oligomerization catalyst to provide one or more higher molecular weight hydrocarbons; and recovering the higher molecular weight hydrocarbons, wherein the at least one oligomerization catalyst comprises H-ZSM-5, B - Al - H-ZSM-5, or a combination thereof, and wherein the at least one bimetallic catalyst is a zero valent metallic alloy that comprises a combination of a first metal chosen from the group consisting of platinum and palladium, and a second metal chosen from the group consisting of manganese, vanadium, chromium and combinations thereof, and a support.",
"11. The process of claim 10, wherein the hydrocarbon containing gas stream is derived from a shale formation.",
"12. The process of claim 10, wherein the hydrocarbon containing gas stream consisting of C 2 to C 4 alkanes contains no isobutane.",
"13. A process for catalytically transforming a natural gas liquid (NGL) into one or more higher molecular weight hydrocarbons, comprising: providing a hydrocarbon containing gas stream that is derived from a shale formation, the hydrocarbon containing gas stream comprising one or more light alkanes chosen from the group consisting of C 2, C 3, and C 4 alkanes; catalytically dehydrogenating at least a portion of the light alkanes to corresponding alkene derivatives; catalytically oligomerizing at least a portion of the alkenes in the presence of at least one oligomerization catalyst to provide one or more higher molecular weight hydrocarbons; and recovering the higher molecular weight hydrocarbons, wherein the at least one oligomerization catalyst comprises: a crystalline microporous zeolite structure having MFI topology, wherein heteroatoms within the zeolite structure are selected from the group consisting of aluminum, gallium, iron and combinations thereof, and wherein trivalent boron atoms within the zeolite structure are substituted for tetravalent silicon atoms.",
"14. The process of claim 13, wherein the group consisting of C 2, C 3, and C 4 alkanes contains no isobutane.",
"15. The process of claim 13, wherein the aluminum, gallium or iron are present in an amount from 0.001 wt % to 30 wt % on an elemental basis of the oligomerization catalyst.",
"16. The process of claim 13, wherein the substitution of trivalent boron atoms for tetravalent silicon atoms do not behave as Brønsted acid sites for catalysis.",
"17. The process of claim 13, wherein a Brønsted acid site that compensate framework boron atoms have low activity compared to those that compensate framework aluminum or gallium or iron atoms.",
"18. The process of claim 13, wherein a Brønsted acid site that compensate framework boron atoms are significantly weaker acid sites compared to those that compensate framework aluminum or gallium or iron atoms.",
"19. The process of claim 13, wherein the boron is present in an amount ranging from 0.001 wt % to 10 wt % on an elemental basis of the oligomerization catalyst."
],
"description_excerpt": "The present disclosure is directed to new hydrocarbon upgrading processes that include the dehydrogenation of light alkanes to their respective alkene derivatives, commonly known as olefins, followed by oligomerization of the light olefins to higher molecular weight hydrocarbon derivatives. The longer chain higher molecular weight hydrocarbons have a greater value than the lighter alkanes.\n\nMore efficient utilization of petroleum and gas reserves is an important strategy for the deployment of future energy generation. Shale gas has become an increasingly important source of natural gas in the United States, and the U.S. government's Energy Information Administration predicts that by 2040, seventy percent of the United States' natural gas supply will come from shale gas. Many of these shale gas formations contain wet gases, which can include substantial concentrations of natural gas liquids (NGL). NGL is a mixture of hydrocarbons made up primarily of ethane (C 2), propane (C 3), butane (C 4), and pentane (C 5). Several major shale gas formations such as Marcellus and Bakken are located far away from historically gas producing and processing region such as the Gulf Coast. These resources can be considered as stranded gas. Also, associated gas, which is a byproduct of shale oil production and may contain substantial concentration of NGL, is generally flared, vented, or injected back to the shale oil reservoir at high cost. Construction of pipelines to transport natural gas liquids to large existing processing plant complexes, such as the Gulf Coast, can be capital intensive.",
"cpc": [
"C10G 59/02",
"B01J 21/02",
"B01J 29/46",
"B25J 9/1697",
"C10G 11/02",
"C10G 11/04",
"C10G 50/00",
"C10G 57/02",
"G06T 15/20",
"G06T 19/20",
"G06T 2207/20081",
"G06T 2207/20084",
"G06T 2219/2016",
"G06T 7/73"
],
"ipc": [
"B01J 21/02",
"B01J 29/46",
"B25J 9/16",
"C10G 59/02",
"G06T 15/20",
"G06T 19/20",
"G06T 7/73"
],
"assignees": [
"Purdue Research Foundation"
],
"inventors": [
"Rakesh Agrawal",
"Jeffrey J. Siirola",
"Taufik Ridha",
"Yiru Li",
"Fabio H. Ribeiro",
"Jeffrey T. Miller"
],
"filing_date": "2023-03-14",
"publication_date": "2025-08-19",
"grant_date": "2025-08-19",
"priority_date": "2017-09-07",
"application_number": "US-202318183377-A",
"family_id": "65634585",
"cited_by_count": 0,
"citations": [
"US4656016A",
"US4751341A",
"US5258564A",
"WO1993016020A2",
"US5264643A",
"US6492548B1",
"US20060102468A1",
"US20110282120A1",
"US20120271085A1",
"US20150158786A1",
"US20140256892A1",
"US20150159099A1",
"US20150157998A1",
"US20160237004A1",
"US20180170838A1",
"US11603500B2"
]
}
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