WO2010076282A1 - Minimal gas processing scheme for recycling co2 in a co2 enhanced oil recovery flood - Google Patents

Minimal gas processing scheme for recycling co2 in a co2 enhanced oil recovery flood Download PDF

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Publication number
WO2010076282A1
WO2010076282A1 PCT/EP2009/067869 EP2009067869W WO2010076282A1 WO 2010076282 A1 WO2010076282 A1 WO 2010076282A1 EP 2009067869 W EP2009067869 W EP 2009067869W WO 2010076282 A1 WO2010076282 A1 WO 2010076282A1
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fraction
hydrocarbons
crude oil
formation
oil
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PCT/EP2009/067869
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French (fr)
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Peter Andrew Marsh
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Shell Internationale Research Maatschappij B.V.
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    • E—FIXED CONSTRUCTIONS
    • E21—EARTH DRILLING; MINING
    • E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
    • E21B43/164—Injecting CO2 or carbonated water
    • 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
    • C10G1/00—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/04—Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L3/00—Gaseous fuels; Natural gas; Synthetic natural gas obtained by processes not covered by subclass C10G, C10K; Liquefied petroleum gas
    • C10L3/06—Natural gas; Synthetic natural gas obtained by processes not covered by C10G, C10K3/02 or C10K3/04
    • C10L3/10—Working-up natural gas or synthetic natural gas
    • C10L3/101—Removal of contaminants
    • E—FIXED CONSTRUCTIONS
    • E21—EARTH DRILLING; MINING
    • E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
    • E21B43/166—Injecting a gaseous medium; Injecting a gaseous medium and a liquid medium
    • E—FIXED CONSTRUCTIONS
    • E21—EARTH DRILLING; MINING
    • E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/34—Arrangements for separating materials produced by the well
    • E21B43/40—Separation associated with re-injection of separated materials
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0204—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the feed stream
    • F25J3/0209—Natural gas or substitute natural gas
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0228—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
    • F25J3/0242—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 3 carbon atoms or more
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/02—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream
    • F25J3/0228—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream
    • F25J3/0247—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by rectification, i.e. by continuous interchange of heat and material between a vapour stream and a liquid stream characterised by the separated product stream separation of CnHm with 4 carbon atoms or more
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
    • F25J3/0605—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the feed stream
    • F25J3/061—Natural gas or substitute natural gas
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
    • F25J3/063—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream
    • F25J3/0645—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream separation of CnHm with 3 carbon atoms or more
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J3/00—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification
    • F25J3/06—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation
    • F25J3/063—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream
    • F25J3/065—Processes or apparatus for separating the constituents of gaseous or liquefied gaseous mixtures involving the use of liquefaction or solidification by partial condensation characterised by the separated product stream separation of CnHm with 4 carbon atoms or more
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2200/00—Processes or apparatus using separation by rectification
    • F25J2200/02—Processes or apparatus using separation by rectification in a single pressure main column system
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2200/00—Processes or apparatus using separation by rectification
    • F25J2200/74—Refluxing the column with at least a part of the partially condensed overhead gas
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2205/00—Processes or apparatus using other separation and/or other processing means
    • F25J2205/02—Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum
    • F25J2205/04—Processes or apparatus using other separation and/or other processing means using simple phase separation in a vessel or drum in the feed line, i.e. upstream of the fractionation step
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2220/00—Processes or apparatus involving steps for the removal of impurities
    • F25J2220/60—Separating impurities from natural gas, e.g. mercury, cyclic hydrocarbons
    • F25J2220/66—Separating acid gases, e.g. CO2, SO2, H2S or RSH
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2230/00—Processes or apparatus involving steps for increasing the pressure of gaseous process streams
    • F25J2230/30—Compression of the feed stream
    • F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F25—REFRIGERATION OR COOLING; COMBINED HEATING AND REFRIGERATION SYSTEMS; HEAT PUMP SYSTEMS; MANUFACTURE OR STORAGE OF ICE; LIQUEFACTION SOLIDIFICATION OF GASES
    • F25J—LIQUEFACTION, SOLIDIFICATION OR SEPARATION OF GASES OR GASEOUS OR LIQUEFIED GASEOUS MIXTURES BY PRESSURE AND COLD TREATMENT OR BY BRINGING THEM INTO THE SUPERCRITICAL STATE
    • F25J2260/00—Coupling of processes or apparatus to other units; Integrated schemes
    • F25J2260/80—Integration in an installation using carbon dioxide, e.g. for EOR, sequestration, refrigeration etc.

Abstract

A minimal gas processing scheme for recycling CO2 in a CO2 enhanced oil recovery process comprises: a) separating a mixture of CO2, crude oil and C1-C6 hydrocarbons produced from the formation into a substantially liquid fraction (6) comprising crude oil and a substantially gaseous fraction (10) comprising CO2 and C1-C6 hydrocarbons; b) separating the substantially gaseous fraction into a first fraction (18) which is enriched in C5-C6 hydrocarbons and a second fraction (12, 14) which is enriched in CO2 and C1-C4 hydrocarbons; c) mixing at least part of the first fraction (18) with the substantially liquid fraction (6) comprising crude oil; and d) recycling at least part of the second fraction (12,14) into the formation.

Description

MINIMAL GAS PROCESSING SCHEME FOR RECYCLING CO2 IN A CO2 ENHANCED OIL RECOVERY FLOOD
The invention relates to a minimal gas processing scheme for recycling carbon dioxide (CO2) in a CO2 enhanced oil recovery method.
It is known to enhance crude oil production by injecting CO2 into the formation such that the CO2 mixes with the crude oil. The thus formed CO2 and crude oil mixture has a lower density and viscosity than the crude oil, resulting in higher oil mobility and therefore higher oil recovery factors. If the crude oil containing formation also comprises natural gas then the natural gas may comprise various components that form after condensation Natural Gas Liquids (NGL's), and which may include Liquefied Natural Gas or LNG (which predominantly comprises methane or (Ci or CH4), Ethane (C2 or C2H6), Liquefied Petrol Gas or LPG (which predominantly comprises propane and butane or C3 and C4) and condensate (which predominantly comprise Cs+ fractions) .
In this specification and accompanying claims the various natural gas and/or Natural Gas Liquid (NGL) fractions are hereinafter identified by the abbreviations Ci, C2, C3, C4, C5 and C5+. Fractions with more carbon atoms per molecule than Ci, C2, C3, C4, C5 are identified as Ci+, C2+, C3+, C4+, C5+. A first reason for separating the C02 from the hydrocarbon gas is that some of the components in the hydrocarbon gas have a negative impact on the miscibility of the CO2 i.e. increase the required reservoir pressure for the CO2 to be miscible with the oil and ultimately lower the incremental oil recovery of the miscible flood. It is known that methane (CH4 or Ci) has a negative impact on miscibility, ethane (C2H6 or C2) and carbon dioxide (CO2) have comparable miscibility, whereas onwards through the hydrocarbon family have a progressively more positive impact on miscibility i.e. decrease the required reservoir pressure for the CO2 to be miscible with the oil and ultimately increase the incremental oil recovery of the miscible flood.
A second reason for separating the CO2 from the hydrocarbon gases is when the capital and operating expenditure required for the gas treatment plant is more than compensated for by the increased revenue from the gas and NGL products from the gas processing facilities. The associated gas from a miscible CO2 EOR flood is often miscible with the oil in the reservoir without any treatment because the positive benefit of the heavier hydrocarbon product counteracts the negative impact of the methane and nitrogen (if present) . As such, gas side economics are more likely to drive the ultimate decision to process or not.
The gas processing required for separating the associated gas from a miscible CO2 EOR flood is generally very complicated and expensive because there is a three phase vapour/liquid/solid region in the phase diagram when separating methane (CH4) and CO2. The solid CO2 prevents the use of conventional fractionation.
Furthermore there is an azeotrope formed between ethane (C2H6) and CO2. An azeotrope is a constant composition boiling mixture where vapour and liquid have the same composition, which makes fractionation of ethane (C2H6) and CO2 impossible. A typical method of overcoming these problems is to use an extractive distillation whereby a third or different component is added to the system to "break" the azeotrope. One such process, which has been widely used for separating CO2 from hydrocarbon within CO2 miscible flood associated gas is known as the Ryan Holmes process, which utilises a C4+ recycle within the process to facilitate separation of the CO2 from the hydrocarbons. The Ryan Holmes process is described in International patent applications WO8301294 and WO9005755, European patent 0129704, US patent application 200304792 and US patents 4318723, 4383842, 4654062, 4675032 and 5335504. The Ryan Holmes process can produce sales grade gas and condensate streams, a liquid CO2 stream, and a C2-C4 LPG stream.
The Ryan Holmes process is equipment intensive, highly energy intensive (in the form of heat), operationally complex and has large inventories of LPG ' s . The Ryan Holmes process is, therefore, not suitable for offshore CO2 miscible flood applications.
Currently, the most widely employed alternative method for separation of CO2 from hydrocarbon within miscible CO2 floods utilizes membranes. Membranes rely on the fact that CO2 permeates faster through a membrane than hydrocarbons.
However, membranes do not produce a sharp separation and it is normal to utilise more than one stage of membranes to effect a reasonable separation. Membranes require significant gas processing upstream to ensure that there are no contaminants (e.g. water, glycol, C6+) in the gas, which would destroy the separating capability of the membranes. This gas treatment is generally expensive . Furthermore, the C02, and other compounds, which permeate across the membranes, drop in pressure considerably across the membranes, thereby requiring expensive compression to raise the pressure back up either for reinjection or for further treatment within the process.
Membranes are often used in conjunction with a secondary process downstream (e.g. amines) in order to obtain reasonably pure CO2 as the membranes do not perform this last stage of separation very efficiently. The membrane process can produce a sales grade gas stream, a vapour CO2 stream, and a C2-C4+ NGL stream. Membranes are generally light in weight, which makes them preferred (particularly for offshore applications), and are operationally simple.
However the process is still energy intensive due to the requirement for large amounts of compression.
From the above it is obvious that the existing first choice processes for gas treatment within CO2 EOR schemes are generally expensive and energy intensive. They also do not take account of the comparative product values of the various products produced within the process in order to optimise the value for every CAPEX (Capital Expenditure) dollar spent. It is an object of the present invention to provide a CO2 EOR minimal gas processing scheme for recycling CO2 in a C02 enhanced oil recovery process which considers the values of the products within the associated gas from a CO2 EOR flood and concentrates on recovering the high value products while ensuring minimal impact on the miscibility of the CO2 stream being reinjected in the CO2 flood. It is a further object of the present invention to provide a method and system, which purify CO2 recycled into a crude oil and Ci-C6 hydrocarbons in a more efficient, reliable and optimum way than the known Ryan Holmes and membrane CO2 purification methods, which are complex, have a high CAPEX and/or are highly energy intensive .
In accordance with the invention there is provided a method for processing and recycling CO2 in a CO2 enhanced oil recovery method from a formation containing crude oil and Ci-C6 hydrocarbons, wherein: a) CO2 is injected into the formation; b) a mixture of CO2, crude oil and Ci-C6 hydrocarbons is produced from the formation; c) the mixture is separated into a substantially liquid fraction comprising crude oil and a substantially gaseous fraction comprising CO2 and Ci-C6 hydrocarbons; d) the substantially gaseous fraction is separated into a first fraction which is enriched in Cs-C6 hydrocarbons and a second fraction which is enriched in CO2 and Ci-C4 hydrocarbons ; e) at least part of the first fraction is mixed with the substantially liquid fraction comprising crude oil; and f) at least part of the second fraction is recycled into the formation.
It is preferred that in step (d) the content of C3- C4 hydrocarbons in the second fraction is controlled such that the ratio between the Ci and the C3-C4 hydrocarbon molar fractions in the second fraction is maintained above a selected threshold value in order to ensure full or partial miscibility of the stream with the oil in the reservoir . In accordance with the invention there is further provided a system for processing and recycling CO2 in a CO2 enhanced oil recovery method from a formation containing crude oil and Ci-C6 hydrocarbons, comprising: a) a first separation assembly for separating a mixture of CO2, crude oil and Ci-C6 hydrocarbons produced from the formation into a substantially liquid fraction comprising crude oil and a substantially gaseous fraction comprising CO2 and Ci-C6 hydrocarbons; b) a second separation assembly for separating the substantially gaseous fraction into a first fraction which is enriched in C5-C6 hydrocarbons and a second fraction which is enriched in CO2 and Ci-C4 hydrocarbons; c) a first outlet conduit connected to the second separation assembly, such as a stabilizer column, for injecting at least part of the first fraction into the substantially liquid fraction comprising crude oil; and f) a second outlet conduit for recycling the second fraction into the formation. It is preferred that the system comprises control means for maintaining the ratio between the C2-C4 and the Ci hydrocarbon molar fractions in the second fraction above a selected threshold value in order to ensure full or partial miscibility of the stream with the oil in the reservoir, such as a mixing conduit through which a selected amount of C5-C6 hydrocarbons from the first fraction is injected into the second fraction.
Said control means may furthermore comprise a Joule- Thompson valve, a Low Temperature Separation (LTS) vessel with temperature control means and a stabilization column with a variable reboiler duty for separating relatively heavy and liquefied C5+ hydrocarbons from relatively light and substantially gaseous CO2 and Ci-C4 with a selected fraction of C3-C4 sufficient to compensate the detrimental effect of Ci on the miscibility of CO2 in crude oil.
These and other features, embodiments and advantages of the method and system according to the invention are described in the accompanying claims, abstract and the following detailed description of preferred embodiments disclosed in the accompanying drawings in which reference numerals are used which refer to corresponding reference numerals that are shown in the drawings.
Figure 1 depicts a flow scheme of the method and system according to the invention;
Figure 2 depicts the value of various hydrocarbons Ci-C5 and crude oil on a barrel of oil equivalent (boe) basis; Figure 3 shows the impact of various components in associated gas on miscibility with crude oil in an Enhanced Oil Recovery (EOR) process;
Figure 4 shows a first alternative flow scheme of the method and system according to the invention; Figure 5 shows a second alternative flow scheme of the method and system according to the invention;
Figure 6 shows a third alternative flow scheme of the method and system according to the invention; and
Figure 7 shows a fourth alternative flow scheme of the method and system according to the invention.
A flow scheme of the method and system according to the invention is shown in Fig.l. In accordance with the invention the values of the products within the associated gas from a CO2 EOR flood are taken in consideration and a balance is provided between recovering the high value products while ensuring minimal impact on the miscibility of the CO2 stream being reinjected in the CO2 flood. Figure 2 is a plot in which the values of the various hydrocarbon products Ci-C5 and crude oil are compared on an equal basis. This equal basis is based on energy equivalence or, calculation of the value of the product on a per Barrel of Oil Equivalent (BOE) basis. It is clear from Figure 2 that the value of the C3, C4 and C5+ (condensate) elements of the associated gas have substantially the same BOE value as crude oil, whereas the Ci and C2 products generally have a product value significantly lower (sometimes almost an order of magnitude lower depending on the local gas market) than the C3+ products.
This observation that methane and ethane have significantly lower values is a relevant insight for the CO2 assisted EOR method and system according to the invention. The above descriptions of the Ryan Holmes and membrane CO2 purification methods indicate why these known methods for separating CO2 from associated natural gas are so complex and expensive, methane and ethane are the very components which are hardest to separate from the CO2 yet they generally have a significantly lower value than the other components in the hydrocarbon gas.
An insight that forms a background of the method and system according to the invention is that it is not optimal to separate out the methane and ethane from associated gas. These components can be left in the CO2 re-injected within the flood as long as sufficient heavier components are also left in the CO2 in order to ensure that the CO2 is sufficiently miscible. Figure 3 shows the impact of various components in associated gas on miscibility with crude oil in an Enhanced Oil Recovery (EOR) process. It shows that Nitrogen (N2) and methane (CH4 or Ci) reduce miscibility, ethane (C2H6 or C2) and carbon dioxide (CO2) have comparable miscibility, whereas propane (C3) , Hydrogen Sulphide (H2S), butane and higher condensates (C5+) have an increasingly positive impact on miscibility. In accordance with the invention the negative impact of methane (Ci) on miscibility is compensated by adding a sufficient amount of C3-C4 compounds to the CO2 and hydrocarbon gas (Ci-C4) containing gas mixture that is recycled through the formation to preserve miscibility of the mixture with the crude oil in the formation.
Figure 1 depicts a process scheme of the method according to the invention. The method according to the invention utilizes standard process unit operations, which are arranged in a novel manner. The novel part of the method and system according to the invention is shown within the dotted line 1 in Figure 1. The method according to the invention uses a standard NGL recovery system comprising a Joule-Thomson valve 2, a Low Temperature Separator [LTS] 3 and cross heat-exchanger 4 in order to drop the temperature of the associated gas in order to drop out the heavier components C5+ from the associated gas. In the LTS 3 a substantially gaseous stream 12 comprising mainly CO2 and Ci-C4 is separated from a condensed liquid stream 12, which has a reduced CO2 and Ci-C4 content. The condensed liquid from the from the LTS 3 is routed to a stabilization column or stabilizer 5 to separate the remaining substantially gaseous stream 14 of CO2 and lighter hydrocarbons Ci-C4 condensed by the JT valve from the substantially liquid stream 14 of NGL ' s . A reboiler 16 is arranged at the bottom of the stabilization column 5 to separate a stream 18 of C5+ from a stream 17 of C4_ hydrocarbons, which latter stream 17 is recycled into the stabilization column 5. The stabilization column 5 is often necessary to reduce large recycles in the system. The condensate contains high percentages of CO2, which if spiked directly into the main oil/gas/water separators (lower operating pressure) simply recycles through the associated gas compression train resulting in large power demand and unstable process operation. The stabilization column 5 removes the majority of the CO2 and lighter hydrocarbons and spikes mainly C5+ hydrocarbons (the high value products) into the oil export stream 6. The CO2 being routed to re-injection contains sufficient C3 and C4 (positive impact on miscibility) to balance the Ci (negative impact on miscibility) . As such, the process according to the invention maximizes recovery of high value products while having no impact on the miscibility of the injected CO2.
Figure 1 furthermore shows that a mixture 7 of crude oil, CO2 and Ci-C6 hydrocarbon fractions is fed from one or more oil production wells (not shown) to a bulk separator 8 in which the substantially liquid crude oil fraction 6 is separated from the substantially gaseous CO2 and Ci-C6 hydrocarbon fractions, and that the stream 10 comprising the substantially gaseous CO2 and Ci-C6 hydrocarbon fractions are compressed in a gas compressor 9 and is then fed to the cross heat exchanger 4.
Benefits of the method and system according to the invention are that they:
-Maximize the recovery of the high value products within the gas; -Do not separate the harder to separate, lower value components within the associated gas; -Have a significantly lower CAPEX than the existing Ryan Holmes and membrane C02 purification schemes. Therefore the method and system according to the invention would have a significantly reduced CAPEX compared with the existing Ryan Holmes and membrane C02 purification options.
Minimal processing equipment would make the method and system according to the invention particularly attractive for offshore applications but also very attractive for onshore applications. A further advantage of the method and system according to the invention is that they utilize existing field proven technology and require no technical step-out using unproven and therefore unreliable technologies. The method and system according to the invention would be simple to operate.
The gas treatment process would not introduce any significant Health Safety and Environment (HSE) issues that would not already be present within the main oil/gas/water separation and compression trains. It will be understood that possible variations to the process scheme shown in Figure 1 are that: -It may be possible to replace the stabilizer with a heated flash in some circumstances, further reducing the cost of the method and system according to the invention. -It may be possible to separate out more LPG's (C3 and C4) from the gas by e.g. providing a condenser at the top of the column in order to produce a liquid LPG stream. This option may be pursued if there was: a. high product value for the LPG's in the intended development location; and/or b. the resulting CO2 was still easily miscible within the reservoir, thereby having no impact on oil recovery from the EOR flood. Some possible variations to the process scheme shown in Figure 1 are shown in Figures 4-7.
In Figures 1 and 4-7 similar components of the alternative embodiments of the system according to the invention are identified by similar references numerals.
Figure 4 shows a process scheme wherein the stabiliser 5 of Figure 1 is replaced by a heated flash assembly 40-43, further reducing the cost of the process. In this alternative process scheme, the condensed liquid stream 13 from the LTS 3 is cross exchanged in a heat exchanger 40 with a warm NGL stream 44 from the heated flash assembly 40-43, and further heated by a heater 41 before being dropped in pressure across a JT valve 42. The two- phase stream is then routed to a separator 43 where a CO2 rich gas stream 45 is separated and recycled back to the CO2 and associated gas mixture 10 upstream of the compressor 9 at the start of the process. The C5+ stream 44 is cross-exchanged with the incoming NGL stream 40 from the LTS 3 and is then routed to export or may also be spiked into the crude oil stream.
Figure 5 shows a second alternative embodiment of the method and system according to the invention wherein more LPG's (C3 and C4) are separated out from the gas if there is: a. a high product value for the LPG's in the intended development location; and/or b. the resulting CO2 still is easily miscible within the reservoir, thereby having no impact on oil recovery from the EOR flood. Figure 5 shows the processing scheme for this utilising the stabiliser column 5 design. The scheme is similar to Figure 1, however, the operating conditions are altered in order to drive C3 and C4 into the NGL liquid product 18. The product 18 is therefore not stabilised. This liquid product 18 could be further separated into sales grade LPG's and condensate in an NGL Fractionation plant (not shown) . Transport to such a plant could be separate to the oil or by spiking into the oil and separating the oil and NGL ' s at a separate location .
Further to the above it may also be possible to operate the alternative processing scheme in Figure 4 in order to drive C3 and C4 into the NGL liquid product. This alternative scheme is shown in Figure 6.
Figure 6 depicts an alternative embodiment of the method and system according to the invention wherein a heated flash similar as shown in Figure 4 is applied and wherein LPG & Condensate (non-stabilised) 44 are exported or spiked into the exported crude oil Stream.
The embodiment shown in Figure 6 is attractive if it is possible to produce a separate LPG (C3 and C4) export stream, again in the situation when there is: a. high product value for the LPG's in the intended development location; and b. the resulting CO2 was still easily miscible within the reservoir, thereby having no impact on oil recovery from the EOR flood.
A possible processing scheme for this option is shown in Figure 7. In this scenario, the column design of the stabilizer 5 would be altered to a condensed/refluxed column i.e. column overhead is condensed in condenser 70 and separated in separator 71 in order to form a liquid product 73 and provide reflux 74 to the stabilizer column 5. Liquid C3/C4 product is produced from the top of the stabiliser separately to the condensate product C5+ stream 18 from the bottom of the stabiliser column 5.

Claims

C L A I M S
1. A method for processing and recycling CO2 in a CO2 enhanced oil recovery method from a formation containing crude oil and Ci-C6 hydrocarbons, wherein: a) CO2 is injected into the formation; b) a mixture of CO2, crude oil and Ci-C6 hydrocarbons is produced from the formation; c) the mixture is separated into a substantially liquid fraction comprising crude oil and a substantially gaseous fraction comprising CO2 and Ci-C6 hydrocarbons; d) the substantially gaseous fraction is separated into a first fraction which is enriched in C5-C6 hydrocarbons and a second fraction which is enriched in CO2 and Ci-C4 hydrocarbons ; e) at least part of the first fraction is mixed with the substantially liquid fraction comprising crude oil; and f) at least part of the second fraction is recycled into the formation.
2. The method of claim 1, wherein steps (b)-(f) are cyclically repeated.
3. The method of claim 1 or 2, wherein in step (d) the content of C3-C4 hydrocarbons in the second fraction is controlled such that the ratio between the Ci and the C3-C4 hydrocarbon molar fractions in the second fraction is maintained above a selected threshold value in order to ensure full or partial miscibility of the stream with the oil in the reservoir.
4. The method of claim 1, wherein the crude oil and at least some other components of the mixture produced in accordance with step (b) of claim 1 are used as feedstock for producing a fuel, lubricant and/or a chemical product .
5. A system for processing and recycling CO2 in a CO2 enhanced oil recovery method from a formation containing crude oil and Ci-C6 hydrocarbons, the system comprising: a) a first separation assembly for separating a mixture of CO2, crude oil and Ci-C6 hydrocarbons produced from the formation into a substantially liquid fraction comprising crude oil and a substantially gaseous fraction comprising CO2 and Ci - C6 hydrocarbons; b) a second separation assembly for separating the substantially gaseous fraction into a first fraction which is enriched in C5-C6 hydrocarbons and a second fraction which is enriched in CO2 and Ci-C4 hydrocarbons; c) a first outlet conduit connected to the second separation assembly for injecting at least part of the first fraction into the substantially liquid fraction comprising crude oil; and f) a second outlet conduit for recycling the second fraction into the formation.
6. The system of claim 5, comprising control means for maintaining the ratio between the C3-C4 and the Ci hydrocarbon molar fractions in the second fraction above a selected threshold value.
7. The system of claim 6, wherein said control means comprise a mixing conduit through which a selected amount of C4-C6 hydrocarbons from the first fraction is injected into the second fraction.
8. The system of claim 6, wherein said control means comprise a Joule-Thompson valve, a Low Temperature Separation (LTS ) vessel and a stabilization column for separating relatively heavy and liquefied C5+ hydrocarbons from relatively light and substantially gaseous CO2 and Ci-C4 with a selected fraction of C3-C4 sufficient to compensate the detrimental effect of Ci on the miscibility of CO2 in crude oil.
PCT/EP2009/067869 2008-12-31 2009-12-23 Minimal gas processing scheme for recycling co2 in a co2 enhanced oil recovery flood WO2010076282A1 (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012040169A1 (en) * 2010-09-21 2012-03-29 Palmer Labs, Llc Method of using carbon dioxide in recovery of formation deposits
US20150152722A1 (en) * 2012-11-29 2015-06-04 Paul Andrew Carmody System and method for realizing added value from production gas streams in a carbon dioxide flooded eor oilfield
EP2889450A1 (en) 2013-12-30 2015-07-01 Air Products And Chemicals, Inc. Process for recovering hydrocarbons from crude carbon dioxide fluid
US9751767B2 (en) 2013-10-02 2017-09-05 Pilot Energy Solutions, Llc Catalytic reactor for converting contaminants in a displacement fluid and generating energy
GB2559418A (en) * 2017-02-07 2018-08-08 Statoil Petroleum As Method and system for CO2 enhanced oil recovery
WO2019071082A1 (en) * 2017-10-06 2019-04-11 Oxy Usa Inc. System and method for oil production separation
GB2597881A (en) * 2017-02-07 2022-02-09 Equinor Energy As Method and system for CO2 enhanced oil recovery

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2875833A (en) * 1954-02-04 1959-03-03 Oil Recovery Corp Process of recovering oil from oil fields involving the use of critically carbonated water
US3084743A (en) * 1958-09-16 1963-04-09 Jersey Prod Res Co Secondary recovery of petroleum
US3228467A (en) * 1963-04-30 1966-01-11 Texaco Inc Process for recovering hydrocarbons from an underground formation
US3480082A (en) * 1967-09-25 1969-11-25 Continental Oil Co In situ retorting of oil shale using co2 as heat carrier
US4318723A (en) 1979-11-14 1982-03-09 Koch Process Systems, Inc. Cryogenic distillative separation of acid gases from methane
US4320802A (en) * 1980-02-11 1982-03-23 Garbo Paul W Use of land-fill gas to stimulate crude oil production and to recover methane-rich gas
WO1983001294A1 (en) 1981-10-01 1983-04-14 Koch Process Systems Inc Distillative separation of methane and carbon dioxide
EP0129704A1 (en) 1983-05-25 1985-01-02 Norton Company Separation of methane rich-gas, carbon dioxide and hydrogen sulfide from mixtures with light hydrocarbons
US4654062A (en) 1986-07-11 1987-03-31 Air Products And Chemicals, Inc. Hydrocarbon recovery from carbon dioxide-rich gases
US4664190A (en) * 1985-12-18 1987-05-12 Shell Western E&P Inc. Process for recovering natural gas liquids
US4675032A (en) 1986-09-29 1987-06-23 Southwest Manufacturers & Distributors, Inc. Vacuum cleaner bag with oscillating tube
US4753666A (en) * 1986-07-24 1988-06-28 Chevron Research Company Distillative processing of CO2 and hydrocarbons for enhanced oil recovery
WO1990005755A1 (en) 1988-11-21 1990-05-31 Collagen Corporation Collagen-polymer conjugates
US5335504A (en) 1993-03-05 1994-08-09 The M. W. Kellogg Company Carbon dioxide recovery process
US20020036086A1 (en) * 2000-04-27 2002-03-28 Institut Francais Du Petrole Process for purification by combination of an effluent that contains carbon dioxide and hydrocarbons
US20030047492A1 (en) 2001-09-04 2003-03-13 Hopewell Richard B. High ethane recovery from a ryan/holmes additive recovery column

Patent Citations (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2875833A (en) * 1954-02-04 1959-03-03 Oil Recovery Corp Process of recovering oil from oil fields involving the use of critically carbonated water
US3084743A (en) * 1958-09-16 1963-04-09 Jersey Prod Res Co Secondary recovery of petroleum
US3228467A (en) * 1963-04-30 1966-01-11 Texaco Inc Process for recovering hydrocarbons from an underground formation
US3480082A (en) * 1967-09-25 1969-11-25 Continental Oil Co In situ retorting of oil shale using co2 as heat carrier
US4318723A (en) 1979-11-14 1982-03-09 Koch Process Systems, Inc. Cryogenic distillative separation of acid gases from methane
US4320802A (en) * 1980-02-11 1982-03-23 Garbo Paul W Use of land-fill gas to stimulate crude oil production and to recover methane-rich gas
WO1983001294A1 (en) 1981-10-01 1983-04-14 Koch Process Systems Inc Distillative separation of methane and carbon dioxide
US4383842A (en) 1981-10-01 1983-05-17 Koch Process Systems, Inc. Distillative separation of methane and carbon dioxide
EP0129704A1 (en) 1983-05-25 1985-01-02 Norton Company Separation of methane rich-gas, carbon dioxide and hydrogen sulfide from mixtures with light hydrocarbons
US4664190A (en) * 1985-12-18 1987-05-12 Shell Western E&P Inc. Process for recovering natural gas liquids
US4654062A (en) 1986-07-11 1987-03-31 Air Products And Chemicals, Inc. Hydrocarbon recovery from carbon dioxide-rich gases
US4753666A (en) * 1986-07-24 1988-06-28 Chevron Research Company Distillative processing of CO2 and hydrocarbons for enhanced oil recovery
US4675032A (en) 1986-09-29 1987-06-23 Southwest Manufacturers & Distributors, Inc. Vacuum cleaner bag with oscillating tube
WO1990005755A1 (en) 1988-11-21 1990-05-31 Collagen Corporation Collagen-polymer conjugates
US5335504A (en) 1993-03-05 1994-08-09 The M. W. Kellogg Company Carbon dioxide recovery process
US20020036086A1 (en) * 2000-04-27 2002-03-28 Institut Francais Du Petrole Process for purification by combination of an effluent that contains carbon dioxide and hydrocarbons
US20030047492A1 (en) 2001-09-04 2003-03-13 Hopewell Richard B. High ethane recovery from a ryan/holmes additive recovery column

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103221632A (en) * 2010-09-21 2013-07-24 帕尔默实验室有限责任公司 Method of using carbon dioxide in recovery of formation deposits
US8869889B2 (en) 2010-09-21 2014-10-28 Palmer Labs, Llc Method of using carbon dioxide in recovery of formation deposits
CN103221632B (en) * 2010-09-21 2017-02-15 帕尔默实验室有限责任公司 Method of using carbon dioxide in recovery of formation deposits
EA026570B1 (en) * 2010-09-21 2017-04-28 Палмер Лэбс, Ллк Method for recovering formation deposits
WO2012040169A1 (en) * 2010-09-21 2012-03-29 Palmer Labs, Llc Method of using carbon dioxide in recovery of formation deposits
US20150152722A1 (en) * 2012-11-29 2015-06-04 Paul Andrew Carmody System and method for realizing added value from production gas streams in a carbon dioxide flooded eor oilfield
US9751767B2 (en) 2013-10-02 2017-09-05 Pilot Energy Solutions, Llc Catalytic reactor for converting contaminants in a displacement fluid and generating energy
US10267560B2 (en) 2013-12-30 2019-04-23 Air Products And Chemicals, Inc. Process for recovering hydrocarbons from crude carbon dioxide fluid
EP2889450A1 (en) 2013-12-30 2015-07-01 Air Products And Chemicals, Inc. Process for recovering hydrocarbons from crude carbon dioxide fluid
GB2559418A (en) * 2017-02-07 2018-08-08 Statoil Petroleum As Method and system for CO2 enhanced oil recovery
WO2018147744A1 (en) * 2017-02-07 2018-08-16 Equinor Energy As Method and system for co2 enhanced oil recovery
CN110325707A (en) * 2017-02-07 2019-10-11 艾奎诺能源公司 For CO2The method and system of intensified oil reduction
US11162342B2 (en) 2017-02-07 2021-11-02 Equinor Energy As Method and system for CO2 enhanced oil recovery
GB2559418B (en) * 2017-02-07 2022-01-05 Equinor Energy As Method and system for CO2 enhanced oil recovery
GB2597881A (en) * 2017-02-07 2022-02-09 Equinor Energy As Method and system for CO2 enhanced oil recovery
GB2597881B (en) * 2017-02-07 2022-08-24 Equinor Energy As Method and system for CO2 enhanced oil recovery
US11702915B2 (en) 2017-02-07 2023-07-18 Equinor Energy As Method and system for Co2 enhanced oil recovery
WO2019071082A1 (en) * 2017-10-06 2019-04-11 Oxy Usa Inc. System and method for oil production separation
US11441410B2 (en) * 2017-10-06 2022-09-13 Oxy Usa Inc. System and method for oil production separation

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