AU2013205480A1 - Carbon Dioxide Enriched Flue Gas Injection for Hydrocarbon Recovery - Google Patents
Carbon Dioxide Enriched Flue Gas Injection for Hydrocarbon Recovery Download PDFInfo
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- AU2013205480A1 AU2013205480A1 AU2013205480A AU2013205480A AU2013205480A1 AU 2013205480 A1 AU2013205480 A1 AU 2013205480A1 AU 2013205480 A AU2013205480 A AU 2013205480A AU 2013205480 A AU2013205480 A AU 2013205480A AU 2013205480 A1 AU2013205480 A1 AU 2013205480A1
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- AU
- Australia
- Prior art keywords
- flue gas
- carbon dioxide
- gas
- set forth
- conditioning unit
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 title claims abstract description 88
- 239000003546 flue gas Substances 0.000 title claims abstract description 58
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 title claims abstract description 57
- 229910002092 carbon dioxide Inorganic materials 0.000 title claims abstract description 45
- 239000001569 carbon dioxide Substances 0.000 title claims abstract description 44
- 238000002347 injection Methods 0.000 title claims abstract description 12
- 239000007924 injection Substances 0.000 title claims abstract description 12
- 238000011084 recovery Methods 0.000 title abstract description 19
- 229930195733 hydrocarbon Natural products 0.000 title description 11
- 150000002430 hydrocarbons Chemical class 0.000 title description 11
- 239000004215 Carbon black (E152) Substances 0.000 title description 9
- 238000000034 method Methods 0.000 claims abstract description 34
- 239000007789 gas Substances 0.000 claims abstract description 29
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 26
- 230000002708 enhancing effect Effects 0.000 claims abstract description 6
- 230000003750 conditioning effect Effects 0.000 claims description 22
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000006227 byproduct Substances 0.000 claims description 7
- 230000009919 sequestration Effects 0.000 claims description 6
- 238000010977 unit operation Methods 0.000 claims description 5
- 230000006835 compression Effects 0.000 claims description 4
- 238000007906 compression Methods 0.000 claims description 4
- 238000010791 quenching Methods 0.000 claims description 4
- 230000018044 dehydration Effects 0.000 claims description 3
- 238000006297 dehydration reaction Methods 0.000 claims description 3
- 238000006477 desulfuration reaction Methods 0.000 claims description 3
- 230000023556 desulfurization Effects 0.000 claims description 3
- 230000003416 augmentation Effects 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 abstract description 19
- 230000008569 process Effects 0.000 abstract description 8
- 230000014759 maintenance of location Effects 0.000 abstract description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 24
- 239000000446 fuel Substances 0.000 description 15
- 239000003921 oil Substances 0.000 description 13
- 239000003345 natural gas Substances 0.000 description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 11
- 230000008901 benefit Effects 0.000 description 11
- 229910052760 oxygen Inorganic materials 0.000 description 11
- 239000001301 oxygen Substances 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000002485 combustion reaction Methods 0.000 description 7
- 239000000295 fuel oil Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 5
- 239000010426 asphalt Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000010248 power generation Methods 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 230000008859 change Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000005431 greenhouse gas Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000002028 Biomass Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000002283 diesel fuel Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000002006 petroleum coke Substances 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 239000002956 ash Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000003190 augmentative effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 239000011335 coal coke Substances 0.000 description 1
- 239000010849 combustible waste Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000001351 cycling effect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 230000003090 exacerbative effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 239000010881 fly ash Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- -1 residuum Substances 0.000 description 1
- 238000009420 retrofitting Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
Classifications
-
- 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
- Y02P90/00—Enabling technologies with a potential contribution to greenhouse gas [GHG] emissions mitigation
- Y02P90/70—Combining sequestration of CO2 and exploitation of hydrocarbons by injecting CO2 or carbonated water in oil wells
Landscapes
- Treating Waste Gases (AREA)
Abstract
A process for enhanced oil and gas recovery. An enriched flue gas is synthesized from utility plant flue gas. The enriched flue gas is customizable for specific requirements; however, the gas is formed to have a high concentration of carbon dioxide. This is used as an injectant for enhancing the liberation of gas and/or oil from subterranean formations. The injection elevates recovery while sequestering carbon dioxide from the power plant source.
Description
P/00/01I Regulation 3.2(2) AUSTRALIA Patents Act 1990 ORIGINAL COMPLETE SPECIFICATION STANDARD PATENT Application No. Lodged: Invention Title: Carbon Dioxide Enriched Flue Gas Injection for Hydrocarbon Recovery The following statement is a full description of this invention, including the best method of performing it known to: 2 CARBON DIOXIDE ENRICHED FLUE GAS INJECTION FOR HYDROCARBON RECOVERY TECHNICAL FIELD [0001] The present invention relates to enhanced hydrocarbon recovery. More specifically, the present invention relates to enhanced oil and gas recovery and carbon dioxide sequestration using carbon dioxide enriched flue gas. BACKGROUND ART [0002] Green house gas has become an escalating concern in the environment and is believed to be contributing to uncharacteristic weather patterns and temperature fluctuations. [0003] The anthromorphic sources of carbon dioxide are largely from industrial and automobile use. In terms of the industrial source, power generation plants factor heavily into the equation. As is typical, North American plants employ coal, natural gas, fuel oil, inter alia to create high pressure steam which is then used to drive steam turbines or used in diesel and gas turbine engines directly for electric power production. This, of course, creates carbon dioxide emissions, exacerbating the emissions problem. [0004] A number of studies and attempts have been recently developed to take advantage of the volumes of carbon dioxide for enhanced oil and gas recovery in subterranean formations. It is well known that such formations, despite having been previously produced to the most economically feasible extent still contain vast reserves of oil and gas. Flue gas injection has now provided an economically viable avenue to continue to produce from the once produced formations. As an attendant feature, carbon dioxide can be sequestered in the formation thus eliminating handling concerns and ensuring compliance with the stringent requirements of the Kyoto accord. [0005] Enhanced hydrocarbon recovery processes use miscible and immiscible gases such as natural gas, natural gas liquids, carbon dioxide, nitrogen, or combustion flue gases maintain pressure, repressurize or expand in a reservoir to push additional oil 3 or natural gas to the wellbore, or use the same or other gases to dissolve in the oil to lower its viscosity and increase its flow rate. [0006] Capture and permanent storage of carbon dioxide in geologic formations has become an increasingly popular option for sequestering carbon dioxide emissions from industrial processes and coal-fired power generation. The U.S. Government is currently developing policies to encourage geologic sequestration with the view of long-term emission reduction. [0007] The costs related to capture of carbon dioxide from power plants, and high purity carbon dioxide sources is high at between $20 to $200 USD per metric ton of carbon dioxide emissions. Capturing and sequestering 90 percent of the carbon dioxide from a new power plant in the United States is estimated to add $0.02 per kilowatt-hour to the cost of electricity, with 75 to 80 percent of the cost for the capture, treatment and injection. Considering that capture technology is a critical aspect of plant design, installing capture technology at existing facilities presents very high costs. The present invention not only addresses capture, but further results in economic recovery of previously uneconomically recoverable hydrocarbons and provides excess usable energy. INDUSTRIAL APPLICABILITY [0008] The aspects of the invention are applicable in the oil and gas industry. DISCLOSURE OF THE INVENTION [0009] Accordingly, an object of the present invention is to provide an improved tertiary oil and/or gas recovery method using a CO 2 enriched flue gas, which method is observant of green house gas concerns. A further important object of one embodiment of the present invention is to provide a sequestration mechanism for carbon dioxide. [0010] A further object of one embodiment of the present invention is to provide a method for enhancing oil and gas production from a subterranean formation containing at least one of gas and oil, comprising providing an energy conversion unit, recovering 4 flue gas from the energy conversion unit, re-circulating the flue gas into said energy conversion unit to form a carbon dioxide enriched stream, and injecting the carbon dioxide enriched stream into the subterranean formation to recover at least one of the gas and oil. [0011] According to another object of one embodiment of the present invention, there is provided a method enhancing oil and gas production from a subterranean formation containing at one of gas and oil, comprising providing an energy conversion unit, providing a source of flue gas, re-circulating the flue gas into the energy version unit to form a carbon dioxide enriched stream, and injecting the carbon dioxide enriched stream into the subterranean formation for sequestration of carbon dioxide in the formation. [0012] Conveniently, in terms of the use of fuel for the process, the method can use any economic fuel source, such as natural gas, sour gas, solution gas, diesel fuel, heavy oil, bitumen, vacuum reside, asphaltene, coal, petcoke, biomass or any suitable combustible waste product. For economic reasons, it is preferred that the feedstock for the fuel be a low cost source, such as from a heavy or extra heavy fraction of bitumen or heavy oil, low cost source, such as from a heavy or extra heavy fraction of bitumen or heavy oil, such as atmospheric or vacuum residuum, asphaltene or visbroken residue. These feedstocks are used to create the Multiphase Superfine Atomized Residue (MSAR
TM
) oil in water emulsion fuel. This alternate fuel is emulsified in the continuous water phase of 10 to greater than 35%wt to create an easily managed liquid fuel that has similar burning characteristics as natural gas. The heavy oil is pre-dispersed in water with surfactant chemistry to produce a consistent droplet size. The immediate benefit is that the fuel achieves greater that 99.99% carbon burnout with similar burning characteristics as with natural gas, in terms of flame length and radiant heat flux. The net benefit is that the least valuable fraction of the feedstock is made into a useful fuel that can be directly adapted to a natural gas boiler or furnace as an economically viable replacement for expensive natural gas. [0013] These and other features, aspects and advantages of the present invention will become better understood with regard to the following description and accompanying drawings.
5 BRIEF DESCRIPTION OF THE DRAWINGS [0014] FIGURE 1 is a schematic illustration of the overall system of the present invention according to a first embodiment; [0015] FIGURE 2 is a schematic illustration of the overall system of the present invention according to a second embodiment; [0016] FIGURE 3 is a graphical representation of the oxygen requirement for flue gas carbon dioxide enrichment on a dry basis; and [0017] FIGURE 4 is a graphical representation of the oxygen requirement for flue gas carbon dioxide enrichment on a wet basis. [0018] For the purpose of the present invention, the following terms are defined below. GHG refers to green house gas; FGT refers to flue gas treatment; FGR refers to flue gas recirculation; HP refers to high pressure; BFW refers to boiler feed water; OTSG refers to once through steam generator; and ECU refers to energy conversion unit. MODES FOR CARRYING OUT THE INVENTION [0019] Referring now to Figure 1, shown is a schematic illustration of one possible 6 embodiment of the apparatus to practice the method. Numeral 10 globally denotes the elements. [0020] An air separation unit operation (not shown) in Figure 1, separates oxygen and nitrogen in an air stream to provide 90% or greater purity oxygen gas 12 for use in the process. This is exemplary; variations are possible depending on the situation. Fuel 14, which may be selected from the non limiting examples of natural gas, sour gas, solution gas, fuel oil, diesel fuel, emulsion fuel, residuum, biomass, coal and petcoke, are mixed with oxygen 12 and 16 forming a fuel mixture for introduction into an energy conditioning unit, generically represented by numeral 18. The energy conversion unit may comprise any suitable device such as a simple cycle, conventional or super critical steam generator circuit with a suitable steam turbine electric generator or steam turbine driven compressors. Other suitable arrangements incorporate a modified gas turbine cogen simple or combined unit with a heat recovery steam generator (HRSG). A further possibility may be a diesel slow speed engine driving an electric generator and/or gas compressor. The specific unit or combination of units will depend upon the design parameters. [0021] As an example, for specific hydrocarbon production sites, a typical electric generation facility would be sized in the 10 to 500 mega watt range or in phases of this size suitable to meet power demands and create sufficient carbon dioxide injection volumes for the enhanced hydrocarbon recovery. The steam driven devices noted above may also include once through steam generators (OTSG), conventional packaged boilers, conventional utility boilers and circulating fluid bed boilers (CFBs) dimensioned to attend to the steam requirement for the electric power generation. [0022] A flue gas recirculation circuit 20 is incorporated into the system for carbon dioxide enrichment. It is well known that a benefit of FGR is the reduction of nitrogen gas in the flue gas and thus the formation of NOx compounds with the concomitant benefit of an increase in the concentration of carbon dioxide in the flue gas. The graphical representations in Figures 3 and 4 depict compositional change for the flue gas for variations in the oxygen content. As an example, the graph in Figure 3 illustrates the clear advantage in carbon dioxide quantity attributed to a high concentration of oxygen resulting from the cycling process through the energy conversion unit. Figure 4 7 demonstrates the same data on a wet basis. [0023] As will be appreciated with an increased oxygen to combustion air ratio for a fixed oxygen concentration, the temperature can become elevated to the extent that design parameters of the boiler/ heat equipment can be exceeded. To counteract this limitation, the flue .gas recirculation circuit can recirculate a combustion stream back to the energy conditioning unit 18 for thermal quenching. As will be appreciated, the quantity of flue gas recirculation will depend on the operational parameters of the equipment. This immediately results in significant advantages, namely: a) enhanced boiler efficiency and operation; b) greater ease for the designer regarding retrofitting of existing plants for the process without extensive re-engineering or equipment replacement; c) improved thermal combustion efficiency; d) reduced NOx emissions; and e) improved safety. [0024] Returning to the overall process, the stream 22 exiting conditioning unit 18, now an enriched flue gas stream, may then be treated in any number of steps, globally denoted by flue gas conditioning unit numerically represented by 24. Generally, the flue gas, depending on the assay of the fuel may contain in addition to C02, such major components as CO, H 2 . excess 02, S02, S03, NOx, N 2 , soot, ash, water vapour metals, etc. The treatment may involve departiculation or flyash removal, flue gas dehydration, quenching, flue gas desulfurization and compression, NOx removal, byproduct recovery or any combination of these. [0025] In addition, based on economic merit, additional methods may be used to recover the useful and valuable byproducts denoted by numeral 26, such as CO, H 2 ,
SO
2 , water and heavy metals for other commercial ventures common to those skilled in the art. As a further clarification, the energy conditioning unit 18 may be operated with 8 combustion of the fuel in a sub-stoiciometric, stoiciometric or excess oxygen mode. Different byproducts can be generated in the enriched flue gas depending on the specific requirements. Typically, it is preferred that the mode be near stoiciometric to produce the highest concentration of carbon dioxide in the enriched flue gas. In some instances, it may be desirable to utilize the byproducts in flue gas design. [0026] The useful energy 28 generated by the energy conditioning unit 18 as one example, may be electric power or direct drive to compress the enriched flue gas and/or combustion air/oxygen in the operations of the flue gas conditioning unit 24. Depending on the design balance of the components and the required volume of the enriched injections flue gas, excess energy 30 may be created and sold to commercial markets as excess electric power. [0027] Residual water 32 discharged from the flue gas conditioning unit 24 may be reused in other processes. Conditioned injection flue gas is transported via line 34 into the subterranean formation 36. The injection flue gas may contain greater than 30% by volume carbon dioxide; however, this will change depending upon the composition of the formation 36 according to Figure 2 and Figure 3. [0028] Formation 36 may contain any one or all of oil, bitumen, heavy oil, natural gas, natural gas liquids or may be used purely for flue gas sequestration [0029] The recovered hydrocarbons leave formation 36 via line 38 and may be subjected to further processing. This is an optional step. [0030] The composition of the treated flue gas is variable and will depend on the specific nature of the content and the physical and chemical properties of the formation. It will be appreciated that the treated flue gas composition may require compositional change dynamically as the formation changes over time. As an example, the composition could be 50% carbon dioxide and 50 % nitrogen to 70% carbon dioxide and 30 % nitrogen through to 100% carbon dioxide. [0031] Turning to Figure 2, shown is a variation in the overall process, where a heat recovery unit 23 is interposed in the circuit between the energy conversion unit 18 and 9 the flue gas conditioning unit 24. In this variation the heat recovery unit 23 is employed to balance the energy produced and maximize the thermal efficiency of the combined cycle method. This arrangement provides for the use of prime movers, e.g. gas turbines and diesel engines. The heat recovery unit 23 may be employed to generate additional steam for electric power generation or be used to preheat water, combustion air or oxygen to elevate the energy efficiency of the method. [0032] The technology set forth has the advantage of enhancing recovery of the values, originally in place, a minimum of 5%; this represents a vast increase in the economics of recovery. This is further augmented by the generation of excess electrical power and/or stream. [0033] In summary, by unifying the concepts of synthesizing an enriched flue gas for injection into a hydrocarbon formation, the following additional advantages are realized: i) Particulate emission reduction; ii) improved carbon burnout; iii) a reduction of N content in flue gas resulting in a volume reduction greater than 60%; iv) economic benefit from increased hydrocarbon production; v) the absence of pipelines and compression devices for the flue 30 gas; vi) self sufficing by generation of electrical power and/or stream for process control; vii) self generation of low cost fuels, such as MSARTM emulsion fuel asphaltenes, residuums; and viii) enhanced energy conversion unit efficiency by use of excess 02
Claims (14)
1. A method for enhancing oil and gas production from a subterranean formation containing at least one of gas and oil, comprising: providing an energy conditioning unit; recovering flue gas from said energy conditioning unit; re-circulating said flue gas into said energy conditioning unit to form a carbon dioxide enriched stream; and injecting said carbon dioxide enriched stream into said subterranean formation to recover at least one of said gas and oil wherein said carbon dioxide is sequestered in said formation.
2. The method as set forth in claim 1, wherein re-circulated flue gas reduces the temperature of said energy conditioning unit.
3. The method as set forth in claim 1, wherein said carbon dioxide enriched stream is treated in at least one conditioning unit.
4. The method as set forth in claim 3, wherein said conditioning comprises a unit operation selected from the group consisting of departiculation, flue gas desulfurization, flue gas quench, flue gas dehydration, flue gas compression, NOx removal and combinations thereof.
5. The method as set forth in claim 1, further including the step of recovering energy generated from said energy conditioning unit.
6. The method as set forth in claim 1, further including the step of selectively recovering byproducts from said method. 11
7. The method as set forth in claim 6, further including the step of utilizing said byproducts for flue gas augmentation.
8. A method for enhancing oil and gas production from a subterranean formation containing at least one of gas and oil, comprising: providing an energy conditioning unit; providing a source of flue gas; re-circulating said flue gas into said energy conditioning unit to form a carbon dioxide enriched stream; and injecting said carbon dioxide enriched stream into said subterranean formation for sequestration of carbon dioxide in said formation.
9. The method as set forth in claim 8, further including the step of selectively recovering gas and oil from said formation.
10. The method as set forth in claim 8, wherein said flue gas recirculation circuit reduces the temperature of said energy conditioning unit.
11. The method as set forth in claim 8, wherein said carbon dioxide enriched stream is treated in at least one conditioning unit operation to modify said carbon dioxide enriched stream prior to injection.
12. The method as set forth in claim 11, wherein said conditioning comprises a unit operation comprises a unit operation selected from the group consisting of departiculation, flue gas desulfurization, flue gas quench, flue gas dehydration, flue gas compression, NOx removal and combinations thereof.
13. The method as set forth in claim 8, further including the step of recovering energy generated from said energy conditioning unit. 12
14. The method as set forth in claim 8, further including the step of selectively recovering byproducts from said method.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2013205480A AU2013205480A1 (en) | 2006-02-07 | 2013-04-29 | Carbon Dioxide Enriched Flue Gas Injection for Hydrocarbon Recovery |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US60/765,749 | 2006-02-07 | ||
| AU2007214212A AU2007214212A1 (en) | 2006-02-07 | 2007-02-07 | Carbon dioxide enriched flue gas injection for hydrocarbon recovery |
| AU2013205480A AU2013205480A1 (en) | 2006-02-07 | 2013-04-29 | Carbon Dioxide Enriched Flue Gas Injection for Hydrocarbon Recovery |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2007214212A Division AU2007214212A1 (en) | 2006-02-07 | 2007-02-07 | Carbon dioxide enriched flue gas injection for hydrocarbon recovery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2013205480A1 true AU2013205480A1 (en) | 2013-05-23 |
Family
ID=48444790
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2013205480A Abandoned AU2013205480A1 (en) | 2006-02-07 | 2013-04-29 | Carbon Dioxide Enriched Flue Gas Injection for Hydrocarbon Recovery |
Country Status (1)
| Country | Link |
|---|---|
| AU (1) | AU2013205480A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114575800A (en) * | 2022-05-05 | 2022-06-03 | 太原理工大学 | A method for in-situ deep in-situ supercritical storage of flue gas |
| CN117703324A (en) * | 2024-01-08 | 2024-03-15 | 西南石油大学 | Device for improving recovery ratio of condensate gas reservoir by injecting carbon dioxide into tight reservoir |
-
2013
- 2013-04-29 AU AU2013205480A patent/AU2013205480A1/en not_active Abandoned
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114575800A (en) * | 2022-05-05 | 2022-06-03 | 太原理工大学 | A method for in-situ deep in-situ supercritical storage of flue gas |
| CN114575800B (en) * | 2022-05-05 | 2022-07-29 | 太原理工大学 | A method for in-situ deep in-situ supercritical storage of flue gas |
| CN117703324A (en) * | 2024-01-08 | 2024-03-15 | 西南石油大学 | Device for improving recovery ratio of condensate gas reservoir by injecting carbon dioxide into tight reservoir |
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| Date | Code | Title | Description |
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| MK4 | Application lapsed section 142(2)(d) - no continuation fee paid for the application |