WO2019221751A1 - Process for renewable fuels using a multistage approach - Google Patents
Process for renewable fuels using a multistage approach Download PDFInfo
- Publication number
- WO2019221751A1 WO2019221751A1 PCT/US2018/033467 US2018033467W WO2019221751A1 WO 2019221751 A1 WO2019221751 A1 WO 2019221751A1 US 2018033467 W US2018033467 W US 2018033467W WO 2019221751 A1 WO2019221751 A1 WO 2019221751A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- beds
- reactors
- reaction zone
- fog
- process according
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
- C10G3/42—Catalytic treatment
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
- C10G3/50—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids in the presence of hydrogen, hydrogen donors or hydrogen generating compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/58—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to change the structural skeleton of some of the hydrocarbon content without cracking the other hydrocarbons present, e.g. lowering pour point; Selective hydrocracking of normal paraffins
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1003—Waste materials
- C10G2300/1007—Used oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1011—Biomass
- C10G2300/1018—Biomass of animal origin
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/02—Gasoline
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- 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
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/08—Jet fuel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P30/00—Technologies relating to oil refining and petrochemical industry
- Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock
Definitions
- the title of the invention is: Process for Renewable Fuels Using a Multistage
- this specification relates to a processes for manufacturing fuels from plant and/or animal fats, oils, and/or greases (“FOG”).
- FOG animal fats, oils, and/or greases
- the specification relates to processes using hydrogenation, decarboxylation, decarbonylation, and/or
- Fig. 1 is a schematic view of a plant operating a process in accordance with the present invention.
- the first stage reactor operates using a lower recycle rate than the primary reactor(s) to increase the residence time (lower LHSV) in the first stage reactor and allows for a smaller first stage reactor.
- the heat generated in the first stage reactor reduces the heat requirement for the primary reactor(s).
- the recycle rate is increased for the primary reactor(s) to limit the exotherm in the primary reactor(s).
- the process according to embodiment 82, wherein the LHSV to the first series of reactors and/or beds is more than 20 hr '1 on a total feed basis.
- concentration is reduced in the reaction zone of the first series of reactors and/or beds below 5 wt% on a fresh feed basis.
- FOG saturation is more than 25% in the reaction zone of the first reactor and/or bed.
- FOG saturation is more than 25% in the reaction zone of the first series of reactors and/or beds.
- FOG saturation is more than 50% in the reaction zone of the first reactor and/or bed.
- FOG saturation is more than 50% in the reaction zone of the first series of reactors and/or beds.
- FOG saturation is more than 75% in the reaction zone of the first reactor and/or bed.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Abstract
The invention relates to a method to reduce the formation of high molecular weight compounds and catalyst coking in the production of renewable diesel. Renewable diesel is produced using hydrogenation, decarboxylation, decarbonylation, and/or hydrodeoxygenation of renewable feedstocks such as animal and/or plant fats, oils, and/or greases (FOG). By first reacting the most reactive species in the FOG in an initial reaction zone prior to the main reaction zone, maximum reaction temperatures and side reactions that lead to the formation of high molecular weight compounds are reduced. This reduces catalyst coking (extends catalyst life) and improves product quality.
Description
The title of the invention is: Process for Renewable Fuels Using a Multistage
Approach
Field of the Invention:
In general, this specification relates to a processes for manufacturing fuels from plant and/or animal fats, oils, and/or greases (“FOG”). In particular, the specification relates to processes using hydrogenation, decarboxylation, decarbonylation, and/or
hydrodeoxygenation in a reaction zone where a liquid recycle stream is used before the first reactor and/or bed where partial conversion takes palace.
Description of the Related Art:
• US Patent Number 8,022,258 B2 states that the formation of high molecular weight compounds can be significantly reduced by having a recycle ratio of at least 5: 1 renewable feed stocks containing more than 5% free fatty acids when using a mild hydrotreating temperature of 280 - 340 °C. US Patent Number 8,022,258 B2 also states that there is significant formation of high molecular weight compounds during hydrotreating for renewable feedstocks containing more than 5% FFAs. In US Patent Number 8,022,258 B2 they found that“Due to the free fatty acids contained in bio oils and fats, the formation of heavy molecular weight compounds is significantly increased compared to triglyceridic bio feeds, which have only low amount of free fatty acids (<1%)”
• US Patent Number 7,982,076 B2 purports to disclose a process for the production of renewable diesel from renewable feedstock using a recycle ration of 2: 1 to 8: 1.
Summary
Brief Description of the Drawings
Fig. 1 is a schematic view of a plant operating a process in accordance with the present invention.
Figs. 2-3 are plots of data from a pilot plant built according to Fig. 1.
Detailed Description
The disclosure relates to a process to reduce the formation of high molecular weight compounds and catalyst coking in the production of renewable diesel. Renewable diesel is produced using hydrogenation, decarboxylation, decarbonylation, and/or
hydrodeoxygenation of renewable feedstocks such as animal and/or plant fats, oils, and/or greases (“FOG”). By first reacting the most reactive species in the FOG in an initial reaction zone prior to the main reaction zone, maximum reaction temperatures and side reactions that lead to the formation of high molecular weight compounds are reduced. This reduces catalyst coking (extends catalyst life) and improves product quality.
Figure l is a schematic view of a pilot plant constructed to carry out the methods disclosed.
Some characteristics of the first reactor and/or bed
• Low activity catalyst
• High liquid hourly space velocity (Total LHSV > 10 hr 1)
• Reduced inlet temperature
• Partial conversion
Example 1
Tests were performed on a 3 million gallon per year plant in Garnett, KS. The results of the test are shown in Table 1. Partial reduction of free fatty acids (“FFA”) was performed in a first stage reactor. The reactor was designed to be able to replace the catalyst online and to protect the primary reactor(s) from catalyst deactivation. Overall total liquid flow to fresh feed ratio for the reactor system was ~ 10 to 1. The total liquid flow to feed ratio for the first stage reactor varied from 2.11 to 4.25. First stage reactor inlet temperature ranged from 575 to 648 °F and initial FFA ranged from 4.96 to 9.98 percent. Percent decrease in FFA did not appear to be significantly affected by inlet temperature or initial percent FFA. Decrease percent of FFA was primarily dependent on the residence time (LHSV). The longer the residence time (lower LHSV) the greater the reduction of FFA (Figure 2).
Using a low activity catalyst at reduced temperature to reduce FFA in the first stage reactor limits side reactions and reduces the formation of heavy molecules while allowing the primary reactor(s) to operate at higher temperatures due to the reduced FFA. Patent US 8,002,258 B2 shows in Example 6 that operating below 626 °F significantly reduces side reactions. Plant data agreed with this showing that the reactor effluent cloud was reduced as the Ist stage reactor inlet temperature decreased, where higher cloud is an indication of the formation of heavy molecules (Figure 3). Patent US 8,002,258 B2 shows in Table 3 that side reactions and the formation of heavy molecules is significantly reduced with the reduction of FFA.
The first stage reactor operates using a lower recycle rate than the primary reactor(s) to increase the residence time (lower LHSV) in the first stage reactor and allows for a smaller first stage reactor. The heat generated in the first stage reactor reduces the heat requirement for the primary reactor(s). The recycle rate is increased for the primary reactor(s) to limit the exotherm in the primary reactor(s).
Table 1
Other Exemplary Embodiments
1. A process that involves the hydrogenation, decarboxylation, decarbonylation, and/or hydrodeoxygenation of animal and/or plant fats, oils and/or greases (FOG) in a reaction zone to form paraffins where the reaction zone is separated into two or more reactors and/or beds where a liquid recycle stream is added before the first reactor and/or bed where the animal and/or plant FOG is partially reacted in the first reactor and/or bed where a liquid recycle stream is added in between two reactors and/or beds in at least one place in a series of two or more reactors and/or beds.
2. The process according to embodiment 1, wherein the LHSV to the first reactor and/or bed is more than 10 hr 1 on a total feed basis
3. The process according to embodiment 1, wherein the LHSV to the first series of reactors and/or beds is more than 10 hr'1 on a total feed basis.
4. The process according to embodiment 1, wherein the LHSV to the first reactor and/or bed is more than 20 hr'1 on a total feed basis.
5. The process according to embodiment 1, wherein the LHSV to the first series of reactors and/or beds is more than 20 hr 1 on a total feed basis.
The process according to embodiment 1, wherein it the first reactor and/or bed outlet temperature is more than the second reactor and/or bed inlet temperature. The process according to embodiment 1, wherein the free fatty acid concentration is reduced in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein the free fatty acid concentration is reduced in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 1, wherein the free fatty acid concentration is reduced in the reaction zone of the first reactor and/or bed below 5 wt% on a fresh feed basis. The process according to embodiment 1, wherein the free fatty acid concentration is reduced in the reaction zone of the first series of reactors and/or beds below 5 wt% on a fresh feed basis. The process according to embodiment 1, wherein FOG saturation is more than 25% in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein FOG saturation is more than 25% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 1, wherein FOG saturation is more than 50% in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein FOG saturation is more than 50% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 1, wherein FOG saturation is more than 75% in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein FOG saturation is more than 75% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 1, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 1, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first series of reactors and/or beds.
The process according to embodiment 1, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 1, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 1, wherein it will be further processed in an isomerization step. The process according to embodiment 1, wherein it will be further processed in an isomerization and/or cracking step to produce a lighter boiling point range product. The process according to embodiment 1, wherein it will be further processed in an isomerization and/or cracking step to produce a jet/kerosene boiling range product. The process according to embodiment 1, wherein it will be further processed in an isomerization and/or cracking step to produce a naphtha/gasoline boiling range product. The process according to embodiment 1, wherein it will be further processed in an isomerization and/or cracking step to produce a fuel gas boiling range product. A process that involves the hydrogenation, decarboxylation, decarbonylation, and/or hydrodeoxygenation of animal and/or plant fats, oils and/or greases (FOG) in a reaction zone to form paraffins where the reaction zone is separated into two or more reactors and/or beds where a liquid recycle stream is added before the first reactor and/or bed at a recycle to fresh feed ratio of less than 5: 1 where the animal and/or plant FOG is partially reacted in the first reactor and/or bed where a liquid recycle stream is added in between two reactors and/or beds in at least one place in a series of two or more reactors and/or beds. The process according to embodiment 28, wherein the LHSV to the first reactor and/or bed is more than 10 hr'1 on a total feed basis. The process according to embodiment 28, wherein the LHSV to the first series of reactors and/or beds is more than 10 hr 1 on a total feed basis.
The process according to embodiment 28, wherein the LHSV to the first reactor and/or bed is more than 20 hr 1 on a total feed basis. The process according to embodiment 28, wherein the LHSV to the first series of reactors and/or beds is more than 20 hr 1 on a total feed basis. The process according to embodiment 28, wherein it the first reactor and/or bed outlet temperature is more than the second reactor and/or bed inlet temperature. The process according to embodiment 28, wherein the free fatty acid
concentration is reduced in the reaction zone of the first reactor and/or bed. The process according to embodiment 28, wherein the free fatty acid
concentration is reduced in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein the free fatty acid
concentration is reduced in the reaction zone of the first reactor and/or bed below 5 wt% on a fresh feed basis. The process according to embodiment 28, wherein the free fatty acid
concentration is reduced in the reaction zone of the first series of reactors and/or beds below 5 wt% on a fresh feed basis. The process according to embodiment 28, wherein FOG saturation is more than 25% in the reaction zone of the first reactor and/or bed. The process according to embodiment 28, wherein FOG saturation is more than 25% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein FOG saturation is more than 50% in the reaction zone of the first reactor and/or bed. The process according to embodiment 28, wherein FOG saturation is more than 50% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein FOG saturation is more than 75% in the reaction zone of the first reactor and/or bed. The process according to embodiment 28, wherein FOG saturation is more than 75% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first reactor and/or bed.
The process according to embodiment 28, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 28, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 28, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 28, wherein it will be further processed in an isomerization step. The process according to embodiment 28, wherein it will be further processed in an isomerization and/or cracking step to produce a lighter boiling point range product.. The process according to embodiment 28, wherein it will be further processed in an isomerization and/or cracking step to produce a jet/kerosene boiling range product. The process according to embodiment 28, wherein it will be further processed in an isomerization and/or cracking step to produce a naphtha/gasoline boiling range product. The process according to embodiment 28, wherein it will be further processed in an isomerization and/or cracking step to produce a fuel gas boiling range product. A process that involves the hydrogenation, decarboxylation, decarbonylation, and/or hydrodeoxygenation of animal and/or plant fats, oils and/or greases (FOG) in a reaction zone to form paraffins where the reaction zone is separated into two or more reactors and/or beds where a liquid recycle stream is added before the first reactor and/or bed where the animal and/or plant FOG is partially reacted in the first reactor and/or bed where a liquid recycle stream is added in between two reactors and/or beds in at least one place in a series of two or more reactors and/or beds
where the combination of all recycle streams to fresh feed ratio is greater than 8: 1. The process according to embodiment 55, wherein the LHSV to the first reactor and/or bed is more than 10 hr 1 on a total feed basis. The process according to embodiment 55, wherein the LHSV to the first series of reactors and/or beds is more than 10 hr 1 on a total feed basis. The process according to embodiment 55, wherein the LHSV to the first reactor and/or bed is more than 20 hr'1 on a total feed basis. The process according to embodiment 55, wherein the LHSV to the first series of reactors and/or beds is more than 20 hr'1 on a total feed basis. The process according to embodiment 55, wherein it the first reactor and/or bed outlet temperature is more than the second reactor and/or bed inlet temperature. The process according to embodiment 55, wherein the free fatty acid
concentration is reduced in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein the free fatty acid
concentration is reduced in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 55, wherein the free fatty acid
concentration is reduced in the reaction zone of the first reactor and/or bed below 5 wt% on a fresh feed basis. The process according to embodiment 55, wherein the free fatty acid
concentration is reduced in the reaction zone of the first series of reactors and/or beds below 5 wt% on a fresh feed basis. The process according to embodiment 55, wherein FOG saturation is more than 25% in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein FOG saturation is more than 25% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 55, wherein FOG saturation is more than 50% in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein FOG saturation is more than 50% in the reaction zone of the first series of reactors and/or beds.
The process according to embodiment 55, wherein FOG saturation is more than 75% in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein FOG saturation is more than 75% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 55, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 55, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 55, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 55, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 55, wherein it will be further processed in an isomerization step. The process according to embodiment 55, wherein it will be further processed in an isomerization and/or cracking step to produce a lighter boiling point range product. The process according to embodiment 55, wherein it will be further processed in an isomerization and/or cracking step to produce a jet/kerosene boiling range product. The process according to embodiment 55, wherein it will be further processed in an isomerization and/or cracking step to produce a naphtha/gasoline boiling range product. The process according to embodiment 55, wherein it will be further processed in an isomerization and/or cracking step to produce a fuel gas boiling range product. A process that involves the hydrogenation, decarboxylation, decarbonylation, and/or hydrodeoxygenation of animal and/or plant fats, oils and/or greases (FOG) in a reaction zone to form paraffins
where the reaction zone is separated into two or more reactors and/or beds where a liquid recycle stream is added before the first reactor and/or bed at a recycle to fresh feed ratio of less than 5: 1 where the animal and/or plant FOG is partially reacted in the first reactor and/or bed where a liquid recycle stream is added in between two reactors and/or beds in at least one place in a series of two or more reactors and/or beds where the combination of all recycle streams to fresh feed ratio is greater than 8: 1. The process according to embodiment 82, wherein the LHSV to the first reactor and/or bed is more than 10 hr 1 on a total feed basis. The process according to embodiment 82, wherein the LHSV to the first series of reactors and/or beds is more than 10 hr 1 on a total feed basis. The process according to embodiment 82, wherein the LHSV to the first reactor and/or bed is more than 20 hr'1 on a total feed basis. The process according to embodiment 82, wherein the LHSV to the first series of reactors and/or beds is more than 20 hr'1 on a total feed basis. The process according to embodiment 82, wherein it the first reactor and/or bed outlet temperature is more than the second reactor and/or bed inlet temperature. The process according to embodiment 82, wherein the free fatty acid
concentration is reduced in the reaction zone of the first reactor and/or bed. The process according to embodiment 82, wherein the free fatty acid
concentration is reduced in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein the free fatty acid
concentration is reduced in the reaction zone of the first reactor and/or bed below 5 wt% on a fresh feed basis. The process according to embodiment 82, wherein the free fatty acid
concentration is reduced in the reaction zone of the first series of reactors and/or beds below 5 wt% on a fresh feed basis. The process according to embodiment 82, wherein FOG saturation is more than 25% in the reaction zone of the first reactor and/or bed.
The process according to embodiment 82, wherein FOG saturation is more than 25% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein FOG saturation is more than 50% in the reaction zone of the first reactor and/or bed. The process according to embodiment 82, wherein FOG saturation is more than 50% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein FOG saturation is more than 75% in the reaction zone of the first reactor and/or bed. The process according to embodiment 82, wherein FOG saturation is more than 75% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 82, wherein FOG conversion to paraffin is less than 50 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 82, wherein FOG conversion to paraffin is less than 25 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first reactor and/or bed. The process according to embodiment 82, wherein FOG conversion to paraffin is less than 10 wt% in the reaction zone of the first series of reactors and/or beds. The process according to embodiment 82, wherein it will be further processed in an isomerization step. The process according to embodiment 82, wherein it will be further processed in an isomerization and/or cracking step to produce a lighter boiling point range product. The process according to embodiment 82, wherein it will be further processed in an isomerization and/or cracking step to produce a jet/kerosene boiling range product.
The process according to embodiment 82, wherein it will be further processed in an isomerization and/or cracking step to produce a naphtha/gasoline boiling range product. The process according to embodiment 82, wherein it will be further processed in an isomerization and/or cracking step to produce a fuel gas boiling range product.
Claims
1. A method for processing animal FOG in a reaction zone to form parafms
comprising: providing a first feed to a reaction zone comprising a plurality of reactors or beds; partially reacting the FOG within a first of the plurality of reactors or beds; providing a second feed to a second of the plurality of reactoros or beds; wherein the first feed includes an unreacted fresh feed component and a first recycled component which is obtained from a point downstream of the reaction zone; and wherein the second feed includes a product component from the first of the reactors or beds and a second recycled component which is obtained from a point downstream of the reaction zone.
2. The method according to claim 1, wherein the LHSV to the first of the plurality of reactors or bed is more than 10 hr'1 on a total feed basis.
3. The method according to claim 1, wherein the LHSV to the first of the plurality of reactors or beds is more than 20 hr'1 on a total feed basis.
4. The method according to claim 1, wherein it an outlet temperature of the first pf the plurality of reactors or beds is greater than an inlet temperature of the second of the plurality of reactors or beds.
5. The method according to claim 1, wherein the free fatty acid concentration of the product component from the first reactor is less than free fatty acid concentration of the first feed.
6. The method according to claim 5, wherein the free fatty acid concentration is reduced in the reaction zone to no more than 5 wt% on a fresh feed basis.
7. The method according to claim 1, wherein FOG saturation is more than 25% in the first of the plurality of reactors or beds.
8. The method according to claim 1, wherein FOG saturation is more than 50% in the first of the plurality of reactors or beds.
9. The method according to claim 1, wherein FOG saturation is more than 75% in the first of the plurality of reactors or beds.
10. The method according to claim 1, wherein FOG conversion to paraffin is less than 50 wt% in the first of the plurality of reactors or beds.
11. The method according to claim 1, wherein FOG conversion to paraffin is less than 50 wt% in the first of the plurality of reactors or beds.
12. The method according to claim 1, wherein FOG conversion to paraffin is less than 25 wt% in the first of the plurality of reactors or beds.
13. The method according to claim 1, wherein FOG conversion to paraffin is less than 10 wt% in the first of the plurality of reactors or beds.
14. The method according to claim 1, wherein a product stream from the reactor zone is further processed in an isomerization step.
15. The method according to claim 1, wherein a product stream from the reactor zone is further processed in an isomerization and/or cracking step to produce a lighter boiling point range product.
16. The method according to claim 15, wherein the product stream from the reactor zone is further processed in an isomerization and/or cracking step to produce a jet/kerosene boiling range product.
17. The method according to claim 15, wherein the product stream from the reactor zone is further processed in an isomerization and/or cracking step to produce a naphtha/gasoline boiling range product.
18. The method according to claim 1, wherein a product stream from the reactor zone is further processed in an isomerization and/or cracking step to produce a fuel gas boiling range product.
19. A method for processing animal FOG in a reaction zone to form parafms
comprising: providing a first feed to a reaction zone comprising a plurality of reactors or beds; partially reacting the FOG within a first of the plurality of reactors or beds; providing a second feed to a second of the plurality of reactoros or beds; wherein the first feed includes an unreacted fresh feed component and a first recycled component which is obtained from a point downstream of the reaction zone and the ratio of the first recycled component to the fresh feed component is less than 5: 1; and
wherein the second feed includes a product component from the first of the reactors or beds and a second recycled component which is obtained from a point downstream of the reaction zone.
20. The method of claim 19 wherein the ratio of a combination of all recycle streams to the fresh feed component is greater than 8: 1.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2018/033467 WO2019221751A1 (en) | 2018-05-18 | 2018-05-18 | Process for renewable fuels using a multistage approach |
EP18919372.5A EP3794092A4 (en) | 2018-05-18 | 2018-05-18 | Process for renewable fuels using a multistage approach |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2018/033467 WO2019221751A1 (en) | 2018-05-18 | 2018-05-18 | Process for renewable fuels using a multistage approach |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2019221751A1 true WO2019221751A1 (en) | 2019-11-21 |
Family
ID=68540812
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2018/033467 WO2019221751A1 (en) | 2018-05-18 | 2018-05-18 | Process for renewable fuels using a multistage approach |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP3794092A4 (en) |
WO (1) | WO2019221751A1 (en) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070010682A1 (en) * | 2005-07-05 | 2007-01-11 | Neste Oil Oyj | Process for the manufacture of diesel range hydrocarbons |
US20090082606A1 (en) * | 2007-09-20 | 2009-03-26 | Marker Terry L | Production of Diesel Fuel from Biorenewable Feedstocks |
US8026401B2 (en) * | 2007-12-20 | 2011-09-27 | Syntroleum Corporation | Hydrodeoxygenation process |
US20120216450A1 (en) * | 2009-09-02 | 2012-08-30 | IFP Energies Nouvelles | Method of converting feeds from renewable sources in co-processing with a petroleum feed using a catalyst based on nickel and molybdenum |
US20150094506A1 (en) * | 2013-09-27 | 2015-04-02 | Uop Llc | Systems and methods for producing fuel from a renewable feedstock |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2008000259A (en) * | 2005-07-04 | 2008-03-11 | Neste Oil Oyj | Process for the manufacture of diesel range hydrocarbons. |
FR2951734B1 (en) * | 2009-10-27 | 2012-08-03 | Inst Francais Du Petrole | METHOD FOR HYDROTREATING CHARGES FROM RENEWABLE SOURCES WITH INDIRECT HEATING |
FR3039160B1 (en) * | 2015-07-24 | 2017-07-28 | Ifp Energies Now | PROCESS FOR HYDROTREATING RENEWABLE MATERIALS WITH AN OPTIMIZED GAS RECYCLE |
-
2018
- 2018-05-18 EP EP18919372.5A patent/EP3794092A4/en active Pending
- 2018-05-18 WO PCT/US2018/033467 patent/WO2019221751A1/en active Application Filing
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070010682A1 (en) * | 2005-07-05 | 2007-01-11 | Neste Oil Oyj | Process for the manufacture of diesel range hydrocarbons |
US20090082606A1 (en) * | 2007-09-20 | 2009-03-26 | Marker Terry L | Production of Diesel Fuel from Biorenewable Feedstocks |
US8026401B2 (en) * | 2007-12-20 | 2011-09-27 | Syntroleum Corporation | Hydrodeoxygenation process |
US20120216450A1 (en) * | 2009-09-02 | 2012-08-30 | IFP Energies Nouvelles | Method of converting feeds from renewable sources in co-processing with a petroleum feed using a catalyst based on nickel and molybdenum |
US20150094506A1 (en) * | 2013-09-27 | 2015-04-02 | Uop Llc | Systems and methods for producing fuel from a renewable feedstock |
Non-Patent Citations (1)
Title |
---|
See also references of EP3794092A4 * |
Also Published As
Publication number | Publication date |
---|---|
EP3794092A4 (en) | 2022-01-05 |
EP3794092A1 (en) | 2021-03-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2019196489A (en) | System and method for renewable fuel | |
US8748680B2 (en) | Process for catalytic hydrotreatment of a pyrolysis oil | |
US10144880B2 (en) | Conversion of triacylglycerides-containing oils to jet fuel range hydrocarbons | |
US20120216450A1 (en) | Method of converting feeds from renewable sources in co-processing with a petroleum feed using a catalyst based on nickel and molybdenum | |
CN104736676A (en) | Process for catalytic cracking a pyrolysis oil | |
CN102373084B (en) | Method producing light fuel oil and propylene from poor residual oil | |
CN102443424B (en) | Method for producing clean diesel from coal tar | |
CN103059973A (en) | Coal tar full-fraction hydrogenation method for coupling slurry bed and static bed | |
US20120090223A1 (en) | Methods for producing diesel range materials having improved cold flow properties | |
CN102344828B (en) | Processing method of inferior residual oil | |
CN102465018A (en) | Coking full-fraction hydrogenation process method | |
WO2010049075A2 (en) | Improved hydrotreatment of renewable organic material | |
CN101434867B (en) | Suspension bed residual oil hydrogenation-catalytic cracking combined technological process | |
CN102559260A (en) | Rear inferior gasoline fraction hydrotreating method for heating furnace | |
EP2756055B1 (en) | Renewable diesel refinery strategy | |
US10358605B2 (en) | Process for renewable fuels using a multistage approach | |
WO2019221751A1 (en) | Process for renewable fuels using a multistage approach | |
CN109722307A (en) | The method and system of processing of heavy oil | |
CN114437792A (en) | Method and apparatus for processing residual oil | |
CN102465036B (en) | Shale oil processing method for producing propylene | |
CN103102900B (en) | Hydrogenation method for producing high quality solvent oil from biological oil | |
CN115261067B (en) | Residual oil hydrogenation method | |
CN103374412B (en) | Combination method for producing high-quality kerosene through hydrogenation | |
CN116948696A (en) | Hydrocracking process for producing heavy naphtha | |
CN103102899B (en) | Hydrogenation method for producing high quality solvent oil from biological oil |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18919372 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2018919372 Country of ref document: EP |