IP Library › Granted Patent US 9,675,956
Granted Patent B2
US 9,675,956 · App. 14/685,781 · Granted Jun 13, 2017

Conversion of triacylglycerides-containing oils

Inventor: Marvin I. Greene (Clifton, NJ)
Assignee: Lummus Technology Inc.
B01J19/24B01J8/02C10G3/40C10G3/50C10G45/00C10G45/06C10G45/08C10G45/10C10G65/12C10G69/06B01J2208/027B01J2219/00103B01J2219/24C10G2300/1011C10G2300/1014C10G2300/1018C10G2300/4081C10G2400/02C10G2400/04C10G2400/08Y02P30/20
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Quick Facts
Patent No.
US 9,675,956
App. No.
14/685,781
Granted
Jun 13, 2017
Kind
B2
Abstract

A process for converting triacylglycerides-containing oils into crude oil precursors and/or distillate hydrocarbon fuels is disclosed. The process may include reacting a triacylglycerides-containing oil-carbon dioxide mixture at a temperature in the range from about 250° C. to about 525° C. and a pressure greater than about 75 bar to convert at least a portion of the triacylglycerides to a hydrocarbon or mixture of hydrocarbons comprising one or more of isoolefins, isoparaffins, cycloolefins, cycloparaffins, and aromatics.

Claims (55)

1. A system for converting triacylglycerides-containing oils into crude oil precursors and/or distillate hydrocarbon fuels, the system comprising:

a mixing device for mixing a triacylglycerides-containing oil feed with carbon dioxide to form an oil-CO2 mixture;

a thermal reforming reactor for reacting the oil-CO2 mixture at a temperature in the range of 250° C. to about 525° C. and a pressure greater than about 75 bar to produce a reaction effluent;

a separator for separating the reaction effluent into a first separation product comprising carbon dioxide and a second separation product comprising hydrocarbon compounds including one or more of isoolefins, isoparaffins, cycloolefins, cycloparaffins, and aromatics; and

a hydrotreater to hydrotreat at least a portion on of the second separation product.

2. The system of claim 1 , further comprising one or more fluid conduits for recycling the first separation product to at least one of the mixing device to form the oil-CO2 mixture and the thermal reforming reactor to control temperature within the thermal reforming reactor.

3. The system of claim 1 , further comprising a fractionator for fractionating hydrocarbons in the second separation product to form one or more hydrocarbon fractions boiling in the naphtha, jet or diesel range.

4. The system of claim 1 , further comprising a fractionator for fractionating hydrocarbons in the hydrotreated product to form one or more hydrocarbon fractions boiling in the naphtha, jet or diesel range.

5. The system of claim 1 , wherein the hydrotreater comprises at least two catalyst beds, and wherein:

a first catalyst bed comprises a catalyst having hydrogenation activity;

a second catalyst bed comprises a catalyst having hydrocracking activity.

6. The system of claim 5 , wherein the catalyst bed proximate an inlet of the hydrotreater comprises a catalyst useful for at least one of:

decarboxylation;

hydrodeoxygenation of unsaturated free fatty acids to produce C5-C24 paraffins;

saturation of mono-, di- and tri-olefins contained in the alkyl backbone of the free fatty acids;

hydrodenitrogenation of trace organic nitrogen compounds; and

catalyst tolerance for water coming in with the hydrocarbonaceous feed.

7. The system of claim 1 , further comprising at least one of:

one or more fluid conduits for co-processing a non-renewable hydrocarbon feedstock with the reaction effluent in the hydrotreater; and

one or more fluid conduits for introducing at least one of water and hydrogen to the triacylglycerides-containing oil feed, the carbon dioxide, or the oil-CO2 mixture upstream of the thermal reforming reactor.

8. A thermal reforming system for converting triacylglycerides-containing oils into hydrocarbons, the thermal reforming system comprising:

a flow conduit for providing a triacylglycerides-containing oil-carbon dioxide mixture;

a thermal reforming reactor configured for reforming, in the absence of an added catalyst, the triacylglycerides-containing oil-carbon dioxide mixture at a temperature in the range from about 250° C. to about 525° C. and a pressure greater than about 75 bar to convert at least a portion of the triacylglycerides to a mixture of hydrocarbons;

a flow conduit for recovering an effluent from the thermal reforming reactor;

a separator for separating the effluent recovered from the thermal reforming reactor into a first separation product comprising carbon dioxide and light reaction byproducts and a second separation product comprising the hydrocarons: and

a gas separation device for separating the carbon dioxide from the light reaction byproducts in the first separation product.

9. The thermal reforming system of claim 8 , further comprising a heat exchanger for heating the triacylglycerides-containing oil-carbon dioxide mixture via indirect heat exchange with the effluent recovered from the thermal reforming reactor.

10. The thermal reforming system of claim 8 , further comprising a flow conduit for introducing additional carbon dioxide to the thermal reforming reactor.

11. The thermal reforming system of claim 8 , further comprising one or more feed lines for mixing water or hydrogen with the triacylglyeerides-containing oil-carbon dioxide mixture upstream of the thermal reforming reactor.

12. The thermal reforming system of claim 8 , wherein the separator is a drum.

13. The thermal reforming system of claim 8 , further comprising:

a hydrotreater for hydrotreating at least a portion of the second separation product; and

a fractionator for fractionating hydrocarbons in the second separation product to form one or more hydrocarbon fractions boiling in the naphtha, jet or diesel range.

14. A thermal reforming system for converting triacylglycerides-containing oils into hydrocarbons, the thermal reforming system comprising:

a mixer for mixing a triacylglycerides-containing oil with carbon dioxide;

a thermal reforming reactor configured for reforming, in the absence of an added catalyst, the triacylglycerides-containing oil-carbon dioxide mixture to convert at least a portion of the triacylgiycerides to a mixture of hydrocarbons;

a flow conduit for recovering an effluent from the thermal reforming reactor;

a feed-effluent exchanger for indirectly heating the triacylglycerides-containing oil-carbon dioxide mixture with the effluent recovered from the thermal reforming reactor;

a drum for separating the effluent into a first separation product comprising carbon dioxide and light reaction byproducts and a second separation product comprising the mixture of hydrocarbons;

a gas separation device for separating the carbon dioxide from the light reaction byproducts in the first separation product;

a recycle system for compressing and recycling the carbon dioxide recovered from the gas separation device;

one or more flow conduits for mixing hydrogen, a non-renewable hydrocarbon feedstock, or a mixture thereof with the second separation product;

a hydrotreater for hydrotreating at least a portion of the second separation product;

a second drum for separating an effluent from the hydrotreater to recover a hydrogen recycle stream and a hydrocarbon stream; and

a fractionation system for fractionating hydrocarbons in the hydrocarbon stream to produce two or more hydrocarbon fractions.

15. The thermal reforming system of claim 14 , further comprising a flow conduit for injecting liquid carbon dioxide into the thermal reforming reactor to maintain a temperature or a temperature profile within the thermal reforming reactor.

16. The thermal reforming system of claim 14 , wherein the hydrotreater comprises at least two catalyst beds, and wherein:

a first catalyst bed comprises a catalyst having hydrogenation activity;

a second catalyst bed comprises a catalyst having hydrocracking activity.

17. The thermal reforming system of claim 16 , wherein the catalyst bed proximate an inlet of the hydrotreater comprises a catalyst useful for at least one of:

decarboxylation;

hydrodeoxygenation of unsaturated free fatty acids to produce C5-C24 paraffins;

saturation of mono-, di- and tri-olefins contained in the alkyl backbone of the free fatty acids;

hydrodenitrogenation of trace organic nitrogen compounds; and

catalyst tolerance for water coming in with the hydrocarbonaceous feed.

Continuity (2)
Division 13711140 · Dec 11, 2012
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