WO2003055960A1 - Composition and method for improving oil recovery - Google Patents

Composition and method for improving oil recovery Download PDF

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Publication number
WO2003055960A1
WO2003055960A1 PCT/US2002/041036 US0241036W WO03055960A1 WO 2003055960 A1 WO2003055960 A1 WO 2003055960A1 US 0241036 W US0241036 W US 0241036W WO 03055960 A1 WO03055960 A1 WO 03055960A1
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Prior art keywords
oil
composition
reservoir
water
surfactant
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PCT/US2002/041036
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French (fr)
Inventor
Edward L. Boudreau
Original Assignee
Boudreau Edward L
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Application filed by Boudreau Edward L filed Critical Boudreau Edward L
Priority to AU2002359795A priority Critical patent/AU2002359795A1/en
Priority to MXPA04005793A priority patent/MXPA04005793A/en
Priority to CA002471137A priority patent/CA2471137A1/en
Publication of WO2003055960A1 publication Critical patent/WO2003055960A1/en

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/58Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
    • C09K8/584Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific surfactants
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/32Materials not provided for elsewhere for absorbing liquids to remove pollution, e.g. oil, gasoline, fat
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02Well-drilling compositions
    • C09K8/32Non-aqueous well-drilling compositions, e.g. oil-based
    • C09K8/34Organic liquids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/52Compositions for preventing, limiting or eliminating depositions, e.g. for cleaning
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/58Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
    • C09K8/592Compositions used in combination with generated heat, e.g. by steam injection
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures
    • C09K8/72Eroding chemicals, e.g. acids
    • C09K8/74Eroding chemicals, e.g. acids combined with additives added for specific purposes
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G1/00Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal
    • C10G1/04Production of liquid hydrocarbon mixtures from oil-shale, oil-sand, or non-melting solid carbonaceous or similar materials, e.g. wood, coal by extraction
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G33/00Dewatering or demulsification of hydrocarbon oils
    • C10G33/04Dewatering or demulsification of hydrocarbon oils with chemical means
    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/16Enhanced recovery methods for obtaining hydrocarbons
    • E21B43/24Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection

Definitions

  • Crude oil or petroleum is a complex liquid mixture of hydrocarbons containing primarily carbon, hydrogen, and varying amounts of other atoms such as sulfur, nitrogen, oxygen, and others. Crude oil is recovered from subsurface oil reservoirs, wherein the oil is held within pores and voids of rock and sand, and then refined to produce a number of useful substances such as gasoline, lubricants and chemical building blocks.
  • Figure 1 illustrates oil production well 110 recovering oil 130 from oil reservoir 120.
  • Production well 110 includes a production line 125 that extends into a volume of the oil held between gas 140 at a top surface and water 150 at a bottom surface.
  • Production well 110 is able to recover the oil from sand and rock that contains it due to pumping action of the well and native pressure of the oil within the reservoir.
  • Figure 2 illustrates oil 230 wetting an outside surface of sand particles 210A-C and within two oil-filled pores 220A-B formed by the sand particles.
  • Such oil wetting of sand may make substantial amounts of the reservoir oil difficult to recover due to strong attractions such as high surface tension forces and capillary forces holding them fixedly to such regions. It may be difficult to remove the oil from such regions by using pressure as the only driving force for removal. Additionally, when water is present external to the pores it may tend to hold the oil inside the pores.
  • FIG. 3 illustrates a steam flooding enhanced oil recover operation to improve oil recovery from a reservoir.
  • Steam addition system 310 comprising a steam generator, a stack gas scrubber, piping, flow control elements, and a steam injection line is used to add or inject steam into oil reservoir 320.
  • the steam heats the oil in the reservoir to reduce the viscosity of the oil and make it less resistive to flow (similarly to the way that honey or molasses flows better when heated). This may allow hot oil proximate sand particle surfaces and within pores to become sufficiently mobile relative to the sand that the oil can move toward oil production well 330 suction inlet and be recovered from the reservoir at the wellhead.
  • a first problem is channeling wherein steam added to the reservoir takes the path of least resistance to the oil production well by improving the recovery of the weakest attached and most available oil first. Once a route to the oil production well has been established further steam flooding has decreased effectiveness due to the easy bypass to the low pressure oil production well.
  • a second problem with steam flooding is that it is less favorable for deep oil reservoirs with high pressures. This is partly due to the increased pressure and heating needs to make the steam suitable for the high reservoir pressures.
  • Figure 1 illustrates an oil production well recovering oil from an oil reservoir.
  • FIG. 1 illustrates difficult to recover oil.
  • Figure 3 illustrates a steam flooding enhanced oil recover operation to improve oil recovery from a reservoir.
  • Figure 4 illustrates a process flow for adding a recovery composition to an oil reservoir and then removing oil from the reservoir.
  • Figure 5 illustrates a process flow for adding a recovery composition to a production well and then removing oil through the well.
  • Figure 6 illustrates a process flow for adding a recovery composition to a production well and using steam flooding.
  • Figure 7 illustrates a process flow for adding a recovery composition according to a cup tool method.
  • Figure 8 illustrates a process flow for adding a recovery composition to a steam well.
  • Figure 9 illustrates a schematic diagram for adding a recovery composition to an injection well.
  • Figure 10 illustrates a schematic diagram of improved recovery of difficult to recover oil with the use of a recovery composition.
  • Figure 11 illustrates a schematic top view of an exemplary oil reservoir field that was treated by an oil recovery composition, the top view showing positions of injection wells and recovery wells control sample of oil recovered from a control well of the exemplary oil reservoir shown in Figure 11, the control sample not affected by the oil recovery composition injected into the oil reservoir.
  • Figure 12 illustrates exemplary gas chromatograph data for a sample of oil taken from well R16 as a control sample.
  • Figure 13A illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well Rl of the oil reservoir shown in Figure 11.
  • Figure 13B illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R2 of the oil reservoir shown in Figure 11.
  • Figure 13C illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R3 of the oil reservoir shown in Figure 11.
  • Figure 13D illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R4 of the oil reservoir shown in Figure 11.
  • Figure 13E illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R5 of the oil reservoir shown in Figure 11.
  • Figure 13F illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R6 of the oil reservoir shown in Figure 11.
  • Figure 13G illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R8 of the oil reservoir shown in Figure 11.
  • Figure 14 illustrates a system for washing oil-contaminated soil with an oil recovery composition.
  • Oil refers to an arbitrarily complex organic liquid mixture of naturally occurring hydrocarbon and other components having arbitrary and widely varying properties such as viscosity, density, color, and composition.
  • the reservoir refers to a subsurface region that contains oil.
  • the reservoir may include a geologic formation or trap of oil wherein the oil is contained within voids and pores of sand, rock, shale, and similar structures.
  • the reservoir may be a terrestrial reservoir or an off-shore reservoir.
  • Viscosity refers to an oil's resistance to flow.
  • Density refers to mass of oil per unit volume. Both viscosity and density affect the ability to get oil to flow to a well bore of a production line and the ability to pump the oil within the line. A high viscosity, high density oil may be more difficult to recover than a low viscosity, low density oil partly because the oil may become trapped within voids in the reservoir and may be difficult to remove from these voids. By way of analogy, it is similarly more difficult to pour honey through a small opening than it would be to pour water through the same opening.
  • Permeability refers to the fluid transmitting measure of a sand or rock material of a reservoir.
  • Mobility refers to the ratio of permeability to viscosity.
  • a recovery composition is described.
  • the recovery composition is suitable for introduction into a reservoir to improve the recovery of oil contained within the reservoir.
  • the recovery composition comprises at least one type of fatty acid alkyl ester.
  • the recovery composition may contain a blend of different fatty acid alkyl esters. In the case of a blend, the different types of fatty acid alkyl esters may be in any proportion that is desired for the particular implementation.
  • Suitable fatty acid alkyl esters for a recovery composition may be represented by the general formula R'COOR wherein R' and R are typically different hydrocarbon groups containing carbon and hydrogen and potentially other components.
  • the groups may contain heteroatoms such as nitrogen, oxygen, sulfur, and others that may be found in organic compounds.
  • the fatty acid alkyl ester may be an ester derived from a triglyceride.
  • the fatty acid alkyl ester may be a vegetable oil lower alkyl ester.
  • the term "lower alkyl ester" refers to an alkyl ester having an R-group of between 1 and 5 carbons inclusive and preferably between 1 and 2 carbons inclusive.
  • R-groups may include such R-groups as methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, and isopentyl.
  • the R-group contains 1 or 2 carbons.
  • the fatty acid alkyl ester may comprise a soy methyl ester or a soy ethyl ester.
  • the R'-group may comprise a carbon chain having between 4 and 22 carbons.
  • the fatty acid alkyl ester is a "long-chain fatty acid alkyl ester" having an R'-group with between 12 and 20 carbons inclusive and preferably between 16 carbons or 18 carbons inclusive.
  • the carbon chain may be saturated and contain no double bonds or be unsaturated and contain one or more double bonds.
  • the fatty acid alkyl ester may comprise a mixture of sixteen carbon chain length methyl esters, seventeen carbon chain length methyl esters, and eighteen carbon chain length methyl esters.
  • the mixture may comprise a linoleic acid methyl ester, an oleic acid methyl ester, a stearic acid methyl ester, and a palmitic acid methyl ester.
  • Triglycerides are oils or lipids that occur naturally in plants and animals.
  • the triglycerides are esters generally characterized by having three molecules of fatty acids linked to glycerol.
  • Different types of triglycerides are contemplated including those present in natural oils of plants, vegetables, corn, spent French-fry oil, olive, palm, coconut, oleaginous seeds, soybean, rapeseed, sunflower, canola, safflower, animals, animal tallow, butter, milk, and others.
  • Table 1 shows approximate fatty acid concentrations in triglycerides from exemplary plant and animal sources.
  • soybean oil triglycerides contain a mixture of fatty acids having either 16 or 18 carbons and generally contain, in largest proportion, unsaturated 18 length carbon chains.
  • Trans-esterification is the process of reacting a triglyceride with an alcohol in the presence of a catalyst to produce an ester and glycerol.
  • soy oil may be trans-esterified with methanol in the presence of a suitable base catalyst such as potassium hydroxide to produce soy derived fatty acid methyl esters plus glycerol as follows:
  • esters may be recovered from the lighter liquid phase and purified as desired.
  • soy methyl ester which belongs to the fatty acid alkyl ester structural class, is commercially available from a number of sources including AG Environmental Products LLC (AEP) of Lenexa, Kansas who offer soy methyl ester under the tradename Soygold R Marine. Soy methyl ester is also known as methyl soyate and biodiesel. Soy methyl ester has been assigned CAS Registry Number 67784-80-9.
  • the Soygold R Marine product comprises in significant proportion C16-C18 fatty acid methyl esters that are derived from soybean oil.
  • Saturated fatty acid methyl esters contained in significant proportion in methyl soyate are methyl esters of lauric acid, palmitic acid, and stearic acid.
  • Unsaturated fatty acid methyl esters contained in significant proportion in methyl soyate are methyl esters of oleic acid, linoleic acid, and linolenic acid.
  • the product is a light yellow colored liquid that has a melting point of about -10°C (a liquid at room temperature), a normal boiling point greater than 200°C (typically 315°C), a vapor pressure typically less than about two millimeters mercury (mmHg) (non-volatile), a specific gravity of about 0.88 g/ml (lighter than water), and very low solubility in water at room temperature.
  • a suitable recovery composition that may be used to improve oil recovery from a reservoir also includes a surfactant 520, a colloid, an acid 530, or some combination.
  • the concentration of the fatty acid alkyl ester may be between about 85% and about 99.89% or preferably between about 94% and about 98.99%.
  • the concentration of the surfactant may be between about 0.1% and about 10% or preferably between about 1% and about 5%.
  • the concentration of the acid may be between about 0.01% and about 5% or preferably between about 0.01% and about 1%.
  • an exemplary concentration may comprise 96% soy methyl ester, 3% F-500TM surfactant (which will be discussed more fully below), and 1% vinegar (more than 4 percent aqueous solution of acetic acid).
  • Suitable surfactants for use in a recovery composition may be any surface active or interfacial agent that gets absorbed at an interface and changes the properties of the interface.
  • the surfactant may be an interfacial tension reducing agent that reduces the interfacial tension of a medium when it is added to the medium.
  • Suitable surfactants may be selected from the group including but not limited to an amphipathic surfactants, anionic surfactant, cationic surfactants, detergents, and soaps.
  • the surfactant may be soluble in the fatty acid alkyl ester composition.
  • the surfactant may be thermally stable at reservoir conditions of temperature, pressure, salinity, and pH.
  • the surfactant may also be comparatively non-toxic.
  • the surfactant may be an amphipathic surfactant having both lyophilic and lyophobic groups.
  • the surfactant may comprise a hydrophobe portion that prefers oil to water and a hydrophile portion that prefers water to oil.
  • the surfactant may be an anionic surfactant that dissociates to yield a surfactant ion whose polar group is negatively charged.
  • Exemplary anionic surfactants include sulfate surfactants (e.g., petroleum sulfates, alkyl sulfates, aryl sulfates), sulfonate surfactants (e.g., petroleum sulfonates, alkyl sulfonates, aryl sulfonates), and others.
  • the surfactant may also be a cationic surfactant that dissociates to yield a surfactant ion whose polar group is positively charged.
  • exemplary cationic surfactants include alkylpyridinium salts and quaternary ammonium salts.
  • the surfactant may also be a detergent formulation that contains other components.
  • the surfactant may be the F-500TM surfactant.
  • F-500TM Dyna-Drill Foamer is a surfactant and foaming additive that is available from BCI Products, of Houston, Texas. This surfactant is commercially available, is comparatively non-toxic, is stable under and additionally may be useful to inhibit flammability of a material onto which it is applied.
  • the surfactant may be a soap made by treating a fatty acid with base to create a sodium or potassium salt of the fatty acid.
  • the surfactant may comprise a saponification product of a fatty acid similar to the fatty acid of the fatty acid alkyl ester.
  • the surfactant may comprise ARMOHIB® 31, ETHOMID® O/17, ETHOMID® HT/23, ETHOFAT® 18/24, ETHOFAT® 242/25, or ARMOHIB® 28, which are all available from Akzo Nobel Chemicals Ltd, of Arnhem the Netherlands, and having other places of business and sales offices.
  • the surfactant may comprise a quaternary amine compound like ARMOHIB® 31, hydrogenated tallow amides like ETHOMID® HT/23, ethoxylated tall oil like ETHOFAT® 242/25, or fatty amines and alkoxylated fatty amines like ARMOHIB® 28.
  • the surfactant may function as an emulsifier, dispersant, oil-wetter, water- wetter, foamer, defoamer or some combination to reduce interfacial tension and capillary forces of the oil within the voids.
  • Surfactants may be costly such that the surfactant may be added to the composition in the smallest proportion that is found to be effective. Suitable surfactants are also preferably not diluted to any significant extent by water, since the water tends to settle out of the oil recovery composition. For example, the surfactant may come as a gel or similar highly viscous liquid.
  • An oil recovery composition may also include a colloid instead of or in addition to a surfactant.
  • colloid will be used to refer to a heterogeneous mixture of a liquid and sufficiently small solid particles.
  • the solid particles may be large enough to scatter a light beam but too small to settle out by gravity.
  • the solid particles may be highly concentrated. Different solid particles are contemplated including inorganic solid particles (e.g., clays), organic solid particles (e.g., starches, polymers, etc.).
  • the solid particles may be less than about 2 microns in diameter.
  • a micelle emulsion is also contemplated wherein the solid particles are replaced by fatty acid soap micelles. Suitable colloids are preferably not diluted with water.
  • the colloid may tend to disperse upon application and therefore aid in the distribution and in particular the lateral distribution of an oil recovery composition through an oil reservoir.
  • the colloid may react with water in a water table to draw the composition into and laterally through the water table from where it may percolate up into the oil reservoir. Accordingly, adding the colloid may encourage improved distribution of the composition within an oil reservoir.
  • One colloid that is contemplated is the TWC210TM colloid, which is commercially available from the Ward Companies of Garden Grove, California.
  • a colloid-containing oil recovery composition may have a concentration of the fatty acid alkyl ester may be between about 65% and about 98.89% or preferably between about 78% and about 93.99%.
  • the concentration of the surfactant may be between about 0.1% and about 10% or preferably between about 1% and about 5%.
  • the concentration of the colloid may be between about 1% and about 20% or preferably between about 5% and about 16%.
  • the concentration of the acid may be between about 0.01% and about 5% or preferably between about 0.01% and about 1%.
  • One contemplated colloid-containing oil recovery composition includes about 90% soy methyl ester, about 5% TWC210 colloid, about 3% essentially undiluted F-500TM surfactant, and about 2% vinegar (dilute acetic acid solution).
  • Another contemplated colloid-containing oil recovery composition includes about 80% soy methyl ester, about 16% TWC210 colloid, about 2% essentially undiluted F-500TM surfactant, and about 2% vinegar.
  • the colloid may be provided in addition to the surfactant, as a partial replacement or substitute for the surfactant, or as a complete replacement of the surfactant in the recovery composition.
  • each amount of surfactant is substituted or replaced by multiple amounts of a colloid.
  • each 1% reduction in surfactant concentration may be accompanied by between about a 1% to 10% or about a 3% to 8% increase in colloid concentration.
  • An acid may be added to the oil recovery composition to aid in suspension of the surfactant, the colloids, or both the surfactant and the colloid in the fatty acid alkyl ester.
  • Suitable acids for the recovery composition may comprise weak acids that do not completely disassociate in water, strong acids that essentially completely dissociate in water, or both a weak acid and a strong acid.
  • Weak acids that are contemplated include an organic acid, carboxylic acid, acetic acid, vinegar comprising about 5% acetic acid in water, formic acid, citric acid, lemon juice, butyric acid, benzoic acid, carbonic acid.
  • the acid comprises acetic acid in the form of vinegar.
  • Strong acids that are contemplated include an inorganic acid, a mineral acid, sulfuric acid, hydrochloric acid, nitric acid, perchloric acid, and others.
  • Preparation of the composition may include adding desired proportions of the surfactant and/or the colloid, and the acid to the fatty acid alkyl ester followed by mixing as desired.
  • Figure 4 illustrates a method 400 for recovering or removing oil from an oil reservoir, according to one embodiment.
  • the method commences at block 401, and then proceeds to block 410, where an effective amount of a recovery composition such as described above is added to an oil reservoir. This may include adding between about 300 gallons and about 3,000 gallons or between about 500 gallons and 1500 gallons per well of a recovery composition.
  • the composition may contain the fatty acid alkyl ester (e.g., a vegetable derived fatty acid methyl ester) at a concentration between about 85% and about 99.89%, a surfactant at a concentration between about 0.1% and about 10% (e.g., F-500), and an acid at a concentration between about 0.01% and about 5% (e.g., acetic acid or citric acid).
  • the composition may be another composition described herein or one that would be apparent to a person having an ordinary level of skill in the art and the benefit of the present disclosure.
  • the recovery composition may affect the oil in the reservoir and in particular may make it easier to recover the oil from the reservoir. It is believed the recovery composition reduces attractions between the oil and the oil containing structures, such as surface tensions, capillary attractions, and physical or chemical bonds between oil and sand. This may make the oil more mobile relative to the sand and rock.
  • the method advances from block 410 to block 420 where oil is removed from the oil reservoir.
  • oil is removed from the oil reservoir.
  • the recovery composition being introduced, it may be possible to remove more oil for a longer period of time than would have been possible if the recovery composition had not been applied.
  • Experimental studies have demonstrated increased oil production for several weeks and even several months at which time the reservoir may be re-treated with the recovery composition.
  • the recovery composition described herein is particularly effective in this regard in comparison to prior art stimulants, because it is believed the recovery composition tends to disperse out into the reservoir with the same effect more effectively than prior art composition. Additional advantages include the fact that the composition is benign relative to production and refining and does not need to be removed from the recovered oil prior to refining.
  • the composition may aid in cleaning or defouling production and refining lines. Additionally, since some fatty acid alkyl esters such as soy methyl ester may be added as a diesel additive, the composition may be recovered during refining to serve a second purpose as an additive and thereby provide both an enhanced oil recovery benefit and also serve as an additive to refining products. The method terminates at block 430. Different methods presented below are contemplated for implementing the addition of recovery compositions as a liquid (or in a substantially liquid state) to oil reservoirs.
  • Figure 5 illustrates a first embodiment wherein the composition is added via a production well.
  • FIG. 6 illustrates a second embodiment wherein the composition is added to a production well and then steam is added to the production well. The steam may assist with distributing the composition to the reservoir, speeding the affect of the composition by decreasing viscosity, and thermally stimulating the oil and composition near the production line.
  • Figure 7 illustrates a third embodiment wherein the composition is added to a well via a cup tool. This embodiment may be useful when the well becomes clogged or fouled and when the oil reservoir has a high water aquifer.
  • Figure 8 illustrates a fourth method wherein the composition is added via a steam line associated with a production well or wells.
  • This embodiment may be useful for reducing viscosity and increasing mobility of heavy oils and may additionally assist with cleaning the steam well. Other methods are contemplated.
  • Figure 5 illustrates a method 500 for recovering or removing oil from an oil reservoir by adding a recovery composition such as described above to a production well, according to one embodiment.
  • the method commences at block 501, and then proceeds to block 510, where a production well is shut down. After shutting down the production well, at block 520 a recovery composition such as described above is added to the oil reservoir by way of the production well (e.g., added down the casing and preferably down the tubing within the casing).
  • the method advances from block 520 to block 530 where the recovery composition is allowed to take affect on the reservoir for a period between about one day and about seven days.
  • the recovery composition After the recovery composition has taken the desired affect on the reservoir at block 540 the production well is started up again and oil is removed from the oil reservoir.
  • the method terminates at block 550. Adding Compositions To Production Wells With Steam Injection
  • Figure 6 illustrates a method 600 for recovering or removing oil from an oil reservoir by adding a recovery composition such as described above to a production well, according to another embodiment.
  • the method commences at block 601, and then proceeds to block 610, where the production well is shut down.
  • a recovery composition is added to the oil reservoir by way of the production well.
  • the recovery composition may be added down the casing or preferably down the tubing.
  • the method advances from block 620 to block 630 where an effective amount of steam is added to the oil reservoir by way of the production well.
  • the effective amount may be an amount sufficient to flush the composition from the line into the reservoir and assist with dispersing the composition into the reservoir.
  • a larger effective amount may also be used to thermally stimulate the oil within the reservoir by heating it to reduce its viscosity. Both of these amounts may depend upon the particular characteristics of the oil field including depth and the oil including viscosity. Accordingly, the amount of steam added may vary from a trivial amount sufficient to flush the line and disperse the composition from the line into the reservoir to a larger conventional amount to thermally stimulate the reservoir. Similarly, characteristics of the steam such as pressure and temperature may vary depending upon depth according to convention.
  • the steam addition may be stopped so that oil recovery may begin.
  • the method advances from block 630 to block 640 where the production well is started up and oil is removed from the oil reservoir. The method terminates at block 650.
  • Figure 7 illustrates a method 700 for recovering oil from an oil reservoir by adding a recovery composition such as described above to a well with a cup tool, according to one embodiment.
  • the method commences at block 701, and then proceeds to block 710, where a well is shut down. After the well has been shut down, at block 1020 a predetermined volume of a recovery composition is added to a cavity or chamber of the cup tool. The method advances from block 720 to block 730 where the cup tool is inserted into the well and the composition is released from the chamber.
  • This may include inserting the cup tool chamber into proximate alignment with perforations in a perforated lining of the well and pressurized blowing the composition from the chamber with sufficient force to inject the composition into the reservoir and to remove oil structures that clog the lining at a particular perforation.
  • the cup tool may assist with targeted distribution and dispersal of the composition and may additionally assist with cleaning deposits from the well.
  • FIG. 8 illustrates a method 800 for recovering or removing oil from an oil reservoir by adding a recovery composition such as described above to a steam line, according to one embodiment.
  • the method commences at block 801, and then proceeds to block 810, where the steam line is shut down. After the steam line has been shut down, at block 820 a recovery composition is added to the oil reservoir by way of the steam line.
  • the method advances from block 820 to block 830 where steam is added to the oil reservoir by way of the steam line to increase the effectiveness of the recovery composition at oil recovery.
  • oil is removed from the oil reservoir.
  • oil may be continuously recovered from the reservoir concurrently with addition of recovery composition at block 820, addition of steam at block 830, or both.
  • the method terminates at block 850.
  • An additional advantage with injecting a recovery composition such as described above is steam well cleaning.
  • Conventionally such steam wells are known to foul with hydrocarbons. This may cause flow restriction or steam dispersal and may limit the amount of steam that can be effectively delivered to the reservoir.
  • One prior art approach for remedying this problem is to inject strong acids into the steam well to remove the hydrocarbons.
  • This approach has the disadvantage of introducing foreign acids into the oil which may cause corrosion of subsequent petroleum refining equipment or which may need to be separated from the oil prior to the petroleum refining processing. Accordingly, cleaning with fatty acid alkyl compositions, which do not cause corrosion during refining, provides an attractive alternative approach.
  • this may allow both cleaning or defouling of the steam well, which may make steam stimulation more effective, as well as concurrently providing the composition to the reservoir to enhance oil recovery.
  • This approach may additionally clean other processing equipment such as pumps that pump the oil from the reservoir and piping which may both be fouled by oil components such as paraffins.
  • a recovery composition may be added via a water injection well and then chased with water.
  • the chase water may be provided in amount sufficient to disperse the composition as well as pressurize the well and mobilize the oil.
  • Still another method includes adding a sufficient amount of the recovery composition as part of a fracing procedure (e.g., prior to pressurizing).
  • Figure 9 illustrates an example application of a soy methyl ester oil recovery composition to an oil reservoir, according to one embodiment.
  • a scrapper tool is inserted into an injection well 950 to open and clear the injection well.
  • the scrapper tool is removed and an injection tool is inserted into the injection well.
  • Water 935 from a separation tank 925 is added to the reservoir 960 via a pump 920.
  • a check valve 945 opens when the pump discharge reaches about 200 psi. This valve may essentially suppress flow from the reservoir.
  • Recovery composition 910 may be added to the injection well from a tanker truck 905 via a pump 915. This may include adding about 100 gallons or more (e.g., as much as 500 gallons or more) of recovery composition to the reservoir.
  • water 935 may be added to push the recovery composition out of the well and into the oil reservoir as shown at 980. This may include adding between about 1 and about 50 times as much water as recovery composition, or more. Generally, the more water available for addition the better since the water aids in dispersing the composition into the reservoir by force of injection, percolation, and other mechanisms. Other segments may be added and these steps repeated as shown at 985 and 990 to vertically disperse the recovery composition along the oil reservoir. Desirably the composition may be dispersed along the oil containing region 970 of the reservoir instead of the gas containing region 965 or water containing region 975.
  • a plurality of segments each having a length between about 10 and about 50 feet are used to disperse the recovery composition over a substantial portion of the oil containing regions 970 of the reservoir.
  • the recovery composition tends to improve recovery of the oil by weakening attachments between the oil and oil containing structures (e.g., sand, rock, shale, etc.).
  • Oil may be recovered from the reservoir via a production well 955 and provided to the separation tank. In the separation tank the produced oil may separate into oil 930, water 935, and solids 940. The oil may be sent to refining and the solids to treatment/disposal.
  • FIG 10 illustrates a recovery composition such as described above interacting with oil wetting sand, according to one embodiment.
  • Sand 1010 is shown having an oil wetted thereto, the oil containing at least some of a recovery composition dissolved therein.
  • a water flood 1030 is coupled with the oil 1020 to remove the oil from the sand.
  • the water flood 1030 may be replaced by another motive fluid or by steam.
  • the sand and the oil meet at an oil-sand interface. Near the interface are an acid (A), a surfactant (S), and a fatty acid alkyl ester (R-O-R') of a recovery composition dissolved in the oil. It is believed that one or more of these composition components act as interfacial agents to reduce attractions and adhesions between the oil and the sand. This is conceptually represented as a dashed line 1070. Advantageously, this tends to make it easier to recover substantial portions of the oil.
  • an acid Near the oil-water interface are an acid, a surfactant, and a fatty acid alkyl ester of the dissolved recovery composition.
  • One or more of these components may act as interfacial agents to reduce interfacial tension between the oil and the water.
  • This is conceptually represented as a dashed line 1060.
  • a portion 1050A containing some of the recovery composition may be dislodged and carried away typically as a droplet of oil 1050B dispersed in the water flood. In such a way the recovery composition may be used to improve recovery of oil.
  • FIG 11 illustrates a top view of an exemplary oil reservoir field 1100 that was treated by an oil recovery composition of the present invention.
  • the top view shows the positions of steam injection wells (II, 12, 13, and 14) and recovery wells (Rl, R2, R3, R4, R5, R6, R8, and control recovery well R16).
  • Recovery compositions containing about 96% soy methyl ester, about 3% F- 500 surfactant, and about 1% vinegar were injected into the steam injection wells before oil samples were recovered from the recovery wells over approximately a three week period.
  • injection well II was injected with 6700 gallons of recovery composition on a first date and five days later with an addition 5,300 gallons of the recovery composition;
  • injection well 12 was injected with 7000 gallons of composition;
  • injection well 13 was injected with 6000 gallons of the recovery composition and 6000 additional gallons of the recovery composition a day later; and injection well 14 was injected with 12000 gallons of the recovery composition.
  • steam was added to each of the injection wells to flush the composition from the lines and disperse the composition into the oil reservoir.
  • oil samples were recovered from each of the recovery wells and tested by gas chromatography.
  • the oil sample collected from control recovery well R16 was not affected by the addition of the composition to the reservoir and serves as a control or benchmark for observing affects on the other oil samples due to addition of the composition.
  • Figure 12 illustrates gas chromatographic data determined for the control sample and Figures 13A-13G show gas chromatographic data determined for samples from wells Rl, R2, R3, R4, R5, R6, and R8, respectively.
  • the gas chromatography data is an analytical representation of the different organic components in each oil sample.
  • the position, shape, curvature, and roughness of the gas chromatography data line characterizes and represents the chemical composition of the oil sample. In this way the data acts as a fingerprint for the oil sample.
  • the gas chromatography data for each collected sample would be expected to be substantially identical within proximate oil wells on the same oil reservoir (i.e., similar to Figure 12).
  • a recovery composition such as those described herein may be used to clean soil that is contaminated with oil.
  • the recovery composition may assist with releasing the oil from the soil by weakening the physical and chemical attractions and attachments between the oil and the soil.
  • FIG. 14 illustrates a two-stage contaminated oil cleaning system 1400, according to one embodiment.
  • the two-stage system includes a primary treatment vessel 1425 and a secondary treatment vessel 1445.
  • the vessels may be enclosed processing tanks having design specifications consistent with the uses and conditions described below.
  • Soil contaminated with oil is added to the primary vessel via a soil hopper 1405.
  • Water and a soil-washing composition are mixed and added to the primary vessel via a water inlet 1410.
  • the water is pressurized water and may be heated between about 100°F to about 200°F or between about 110°F and about 130°F. Enough water may be added to provide a good flush of the soil through and from the system including the vessels.
  • the composition may be added in a ratio to the soil of about 0.01 to about 10 or between about 0.1 and about 2.
  • the composition may comprise 80( ⁇ 6)% soy methyl ester, 18( ⁇ 5)% TWC210 or similar colloid, and 2( ⁇ 1)% vinegar. Alternatively, other compositions described herein may be used instead.
  • the primary vessel may be an elongated vessel having a long side along which the soil may travel from an entrance end at the inlets to an opposite end.
  • the water inlet and hopper may be located on or proximate the entrance side.
  • the water inlet and the hopper may additionally be located proximate one another towards a top of the primary vessel and aligned so that the water directs and mixes the soil downward due to its velocity.
  • Compressed air may be added to the primary vessel via an air inlet 1415.
  • the air may be added in an amount sufficient to agitate the primary vessel contents including enough to mix the soil and the water-composition mixture.
  • the air inlet may direct the air in a direction along a longest side of the vessel so as to encourage the water and soil in the tank to move in this direction. According to one embodiment at least some of the air is added upward along the length of the bottom of the vessel to encourage soil not to settle and pack, which may decrease the washing efficiency.
  • Spent air may exit the vessel through a spent air treatment system 1420, which may include a venturi and air scrubber.
  • the soil and water move across the tank, from the entrance at the left to an exit at the right, and is removed from the primary vessel by a pumping system 1430.
  • the primary vessel may have a size sufficient to provide an effective residence time for the composition and water to wash the soil.
  • the residence time may be between about 1 minute and 5 hours or preferably between about 5 minutes and 1 hour.
  • the water and the soil washing composition loosen and remove an effective amount of the oil from the soil.
  • the removed oil and the composition may separate from the water as droplets within the water and may rise to an oil layer at the top of the primary vessel. According to one embodiment, this layer is skimmed, pumped, or otherwise removed from the primary vessel for further processing.
  • a pumping system 1430 pumps the soil and water to a secondary treatment vessel 1445.
  • the pumping system may comprise a gravel pump.
  • the secondary vessel may be substantially as described for the primary vessel or may be different as desired.
  • the soil mixture may enter the secondary vessel at a left hand entrance (as viewed) and travel from left to right along a longest length of the vessel to an exit side at the left.
  • Water may be added via a water inlet 1440 to assist with movement of the soil and air may be added via an air inlet 1435 to assist with agitation of the vessel contents.
  • the spent air may leave through a spent air treatment system 1450. Phase separated oil and composition may be skimmed and recovered from the secondary vessel or pumped out with the water for subsequent processing and recovery.
  • a pumping system 1455 removes water and soil from the secondary vessel at an opposite side from its inlet and pumps it to a dewatering system 1460.
  • the dewatering system may comprise a dewatering means such as a large settling tank, shaker pit to shake out solids, a centrifuge, or some combination.
  • the recovery composition describe herein may be used as oil spill agent to recover or remove oil from an oil spill.
  • the recovery composition may be used to coat surfaces before contacted with the oil spill or to weaken bonds between oil and surfaces after they have been coated with oil.
  • a first method for recovering or removing oil from an oil spill may include: (1) spraying or otherwise applying an effective amount (e.g., between about 0.01-1 gallon per square foot or preferably about 0.1 gallons per square foot depending upon the amount of oil) of the recovery composition on environmental surfaces (e.g., rocks, sand, beaches, piers, boat docks, etc) that have been coated by oil from a spill, (2) allowing sufficient time for the composition to loosen the bonds between the oil and the soil (e.g., between about one minute and one day or preferably between about 0.5-2 hours, (4) spraying water on the soil to remove the oil from the soil, (5) collecting the removed oil, and (6) repeating (l)-(5) zero or more times until the oil has been removed to a desired extent.
  • an effective amount e.g., between about 0.01-1 gallon per square foot or preferably about 0.1 gallons per square foot depending upon the amount of oil
  • environmental surfaces e.g., rocks, sand, beaches, piers, boat
  • a second method may include spraying or otherwise applying the recovery composition on surfaces before they are coated with oil to make the surfaces less susceptible to strong coating attachment by the oil. For example, following an oil spill on the sea a proximate beach may be sprayed with an effective amount of the recovery composition (e.g., about 0.1 gallons per square foot) before the oil spill reaches the beach to prevent the approaching oil spill from adhering strongly to the surfaces.
  • an effective amount of the recovery composition e.g., about 0.1 gallons per square foot
  • This may reduce the impact of the spill as well as making remediation easier and less costly.
  • the exemplary composition mentioned above for cleaning oil contaminated soil is also contemplated to be useful for this embodiment.
  • Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
  • the recovery composition described herein may be used to improve separation of solids from oil and water.
  • the recovery composition may be added to production oil or water pumped from the well to release solids suspended by the oil or water by weakening the attractions between the solids and the fluids.
  • the recovery composition may reduce bonding between the solids and the fluids and allow them to separate by gravity. This may allow the oil and water to pass though to the production process with significantly reduced solids.
  • this may reduce wear to processing equipment such as pumps and valves.
  • This may also allow the solids to be recovered cleaner from knockouts and tanks than is possible by current methods involving polymers.
  • such cleaner solids may be considered less hazardous materials for purposes of disposal, storage, or treatment.
  • a method for improving solids separation with the recovery composition may include: (1) adding an effective amount of a recovery composition, e.g., between about 0.01-0.1 gallons per gallon of fluid, to a process fluid (e.g., oil or water pumped from the well), (2) allowing sufficient contact (e.g., sufficient mixing within a valve or sufficient time within a tank or other high residence time equipment) to allow the recovery composition to contact the suspended solids, (3) allowing sufficient time for the composition to loosen the bonds between the oil and the soil and for the suspended solids to settle (e.g., between about one minute and one day or preferably between about five minutes and one hour depending upon the size of the density and size of the solids and the viscosity of the oil, and (4) conventionally processing the separated fluids and solids.
  • a process fluid e.g., oil or water pumped from the well
  • allowing sufficient contact e.g., sufficient mixing within a valve or sufficient time within a tank or other high residence time equipment
  • An example recovery composition that is contemplated to be useful for this embodiment includes 90( ⁇ 5)% soy methyl ester and 10( ⁇ 5)% TWC210 colloid. Acid may not be needed to provide suspension of the colloid since the composition may remain thoroughly mixed by flow, pumping, and similar means. Additionally, the composition may remain mobile rather than stagnant, which would promote separation. Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
  • the recovery composition may be used as a cleaning agent to remove oil component fouling from oil processing equipment.
  • the recovery composition may also be used to clean the inside or outside of oil processing equipment such as knock out tanks, storage tanks, production lines, pipes, valves, pumps, and other processing equipment in order to remove oil component fouling such as organic residue, hydrocarbon fouling, or cake.
  • the recovery composition may be more compatible with the refining process than other cleaning agents such as acids.
  • the composition and in particular the surfactants may also aid in reducing H 2 S levels.
  • a method for removing oil component fouling from an evacuated tank may include: (1) spraying or otherwise applying an amount of the recovery composition sufficient to coat the surface of the tank (e.g., typically less than about 0.01 gallons per square foot of tank, (2) allowing sufficient time for the composition to loosen the bonds between the fouling and the tank (e.g., between about 1 minute and 1 day or preferably between about 0.5-2 hours, (4) spraying water preferably a high pressure stream of water on the tank to remove the fouling and the recovery composition from the tank, (5) disposing of the removed fouling and composition, and (6) repeating (l)-(5) zero or more times until the tank has been cleaned to a desired extent.
  • an amount of the recovery composition sufficient to coat the surface of the tank (e.g., typically less than about 0.01 gallons per square foot of tank, (2) allowing sufficient time for the composition to loosen the bonds between the fouling and the tank (e.g., between about 1 minute and 1 day or preferably between about 0.5-2 hours, (4) spraying water preferably
  • a method for removing fouling from less accessible processing equipment such as production lines, pumps, and valves is also contemplated.
  • pure composition or solutions (e.g., diluted with water) of the recovery composition may be circulated through the processing equipment.
  • this may be used to remove oil fouling such as paraffin and asphalt deposits from such inaccessible processing equipment.
  • An example recovery composition that is contemplated to be useful for this embodiment includes 80( ⁇ 8)% soy methyl ester, 5(+2)% F-500 surfactant, 13( ⁇ 5)% TWC210 colloid, 2( ⁇ 1)% vinegar.
  • Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
  • a similar recovery composition and method as described above to remove fouling may be used to remove oil-based paint or graffiti from surfaces.
  • a similar recovery composition may also be used to remove oil components from cement, such as parking garage floors.
  • the recovery composition may be used to clean wildlife such as birds and animals that are contaminated by oil, such as by an accidental oil spill.
  • the recovery composition may weaken the bonds between feathers, fur, and skin and the oil.
  • this may reduce the impact of the spill on the wildlife and may allow cleaning the wildlife with a non-toxic, non- irritating, and biodegradable agent.
  • a method for cleaning wildlife may include: (1) restraining the wildlife such as by hand or within a cage, (2) spraying or otherwise applying an amount of the recovery composition sufficient to coat the surface of the wildlife (e.g., less than about one gallon or preferably less than about 0.1 gallon per animal the size of a normal ptarmigan), (3) massaging the recovery composition into contact with the animals fur or features, (4) allowing sufficient time for the composition to loosen the bonds between the oil and the fur or feathers (e.g., between about thirty seconds and about one hour or preferably less than about ten minutes, (5) gently spraying water on the wildlife to remove the oil and the recovery composition from the fur or feathers, and (6) repeating (2)-(5) zero or more times until the wildlife has been cleaned to a desired extent.
  • an amount of the recovery composition sufficient to coat the surface of the wildlife (e.g., less than about one gallon or preferably less than about 0.1 gallon per animal the size of a normal ptarmigan)
  • composition that is contemplated to be useful for this embodiment includes 90( ⁇ 5)% soy methyl ester, 8( ⁇ 4)% lanoline, and 2( ⁇ 1)% aloe vera. These components and concentrations may be replaced with other non-toxic and non-irritating components and concentrations.
  • the lanoline may be replaced by another surfactant used in cleaning agents for humans such as bath soaps, shampoos, and cleaners that are sufficiently mild for humans.
  • Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
  • the recovery composition may be used to remove water from oil by breaking an oil-water emulsion.
  • Oil recovered from reservoirs often contains oil-water emulsions.
  • An emulsion is a liquid mixture of two or more liquid substances that are not normally dissolved in one another. One liquid is held in suspension in the other liquid. In the water-in-oil emulsion the water is the suspended minority liquid and oil is the suspending majority liquid. The amount of water may depend upon the chemical characteristics of the oil and how it is produced. Many oils contain emulsifying agents.
  • Exemplary emulsifying agents include solid particles (e.g., silt, drilling mud, or clay particles), naturally occurring surfactants, and certain chemicals that may be added during production (e.g., corrosion inhibitors, scale controllers, paraffin controllers, and the like).
  • the water, the oil, and any emulsifying agents that are present may become intimately mixed and emulsified during turbulent mixing and shearing processes that occur in pumps, valves, pipes, and other production equipment.
  • oil-water emulsions may contribute to numerous problems during transport in pipelines and during refining.
  • One problem is that the water may contain corrosive materials (e.g., salts, acids, etc.) that may damage pipelines and refining equipment.
  • Another problem is that the water constitutes additional fluid that needs to be transported and refined, which increases the costs.
  • Yet another problem is that the emulsions have high viscosity, which may lead to pumping problems, and may accumulate on separators, leading potentially to dangerous conditions and costly, labor intensive production shutdowns. Due to these problems, and others, many pipeline companies, and refining companies, have set specifications, often known as BS&W (bottom sediment and water) specifications, which limit the amount of water in the oil for purposes of transport via pipeline or refining.
  • BS&W bottom sediment and water
  • the oil is often tested, for example with a BS&W monitor which detects entrained water content in oil due to the water changing the capacitive reactance as a function of the dielectric constant, and additional costs may be imposed, or services refused, if the water content is higher than specified.
  • the stability of the emulsion depends upon the characteristics of the oil and water, and the way in which they are mixed. Given sufficient time, most emulsions will break. However, prolonged processing times are generally not desirable in commercial oil production.
  • chemicals known as emulsion breakers are often added to the oil to destabilize or break the oil- water emulsions and encourage gravimetric separation of the water from the oil, in which it was mixed, based on differences in density. This process is known as chemical demulsification.
  • Existing chemicals have a number of limitations and there is a general need in the art for new demulsification compositions.
  • a method for demulsifying an oil-water emulsion may include adding a composition containing a fatty acid alkyl ester, a surfactant, and an acid, to the oil-water emulsion to thereby form a mixture, and permitting a phase separation to occur within said mixture to thereby produce an oil phase and a water phase. At least a portion of the resulting oil phase may be processed and at least a portion of the resulting water phase may be disposed.
  • the demulsification may be practiced offshore and the at least a portion of the separated water disposed offshore.
  • Embodiments of compositions and methods may help oil producers meet water content specifications set for pipelines and refineries, and in general may help to reduce equipment corrosion, processing costs, downtime, and other problems associated with the water.
  • compositions described herein are suitable for breaking oil-water emulsions.
  • the composition may comprise a concentration of the fatty acid alkyl ester that may be between about 85% and about 99.89%, the concentration of the surfactant may be between about 0.1% and about 10%, and the concentration of the acid may be between about 0.01% and about 5%.
  • the concentration of the fatty acid alkyl ester may be at least about 85%
  • the concentration of the surfactant such as TWC210 colloid or F-500TM surfactant or some combination
  • the concentration of the acid such as vinegar, similarly dilute weak organic acid solution, or other similarly dilute acid solution
  • Such compositions achieve a rapid separation of the water from the oil, essentially break the entire emulsion, provide a sharp interface between a lower oil phase and an upper water phase, and provide a substantially pure water phase.
  • the relative proportions of fatty acid alkyl ester, surfactant, and acid may be customized, at least to some extent, based on the nature of an oil-water emulsion for a particular reservoir or field.
  • a pump or metering device may be used to add the composition to the emulsion.
  • the composition may be added manually.
  • the composition may be added to the emulsion in a phase separation vessel, such as a tank, or at the inlet piping to the vessel.
  • a vessel may be favored because it may have a size that facilitates gravity settling of water droplets from the oil.
  • the vessel is not required and the composition may also be added to an emulsion flowing through a pipe or pipeline without the vessel.
  • the composition may be mixed with the emulsion to give a concentration of the composition in the range of approximately 1-1000 ppm (parts per million). Higher concentrations may also be used.
  • the method may further include mixing the composition with the emulsion.
  • the mixing may be achieved by using an agitator, such as a motorized stirrer with a plurality of mixing blades, or by circulating the mixture through a pipe, elbow, valve, pump, or similar mixing device.
  • compositions and method for demulsifying an oil-water emulsion resulting from the production of crude oil from a subsurface crude oil reservoir may be of great assistance and economic benefit to oil producers in helping them meet water content specifications for pipelines and refineries and in general reducing the problems associated with oil-water emulsions.

Abstract

A method and composition are described for improving recovery of oil from an oil reservoir. The method includes adding an effective amount of a fatty acid alkyl ester oil recovery composition to an oil reservoir and recovering oil from the reservoir. A composition including in predominant proportion a fatty acid alkyl ester as well as effective concentrations of a surfactant and/or colloid, and an acid. One exemplary composition includes 96% soy methyl ester, 3% surfactant, and 1% vinegar. A method for improving recovery of oil from an oil reservoir including adding a composition including a fatty acid alkyl ester, a surfactant and/or colloid, and an acid. Also methods for breaking an oil-water emulsion and a method for cleaning oil-contaminated soil, objects and wildlife.

Description

COMPOSITION AND METHOD FOR IMPROVING OIL RECOVERY
BACKGROUND
Field
Methods and compositions for improving oil recovery from a reservoir, and cleaning contaminated soil, objects, and wildlife.
Background Information
Crude oil or petroleum is a complex liquid mixture of hydrocarbons containing primarily carbon, hydrogen, and varying amounts of other atoms such as sulfur, nitrogen, oxygen, and others. Crude oil is recovered from subsurface oil reservoirs, wherein the oil is held within pores and voids of rock and sand, and then refined to produce a number of useful substances such as gasoline, lubricants and chemical building blocks.
Figure 1 illustrates oil production well 110 recovering oil 130 from oil reservoir 120. Production well 110 includes a production line 125 that extends into a volume of the oil held between gas 140 at a top surface and water 150 at a bottom surface. Production well 110 is able to recover the oil from sand and rock that contains it due to pumping action of the well and native pressure of the oil within the reservoir.
Recovery of oil such as that shown in Figure 1 is comparatively easy when the oil is light, has a low viscosity, the reservoir is full of oil, and the reservoir has a high pressure. However, recovery of the oil becomes more challenging when these conditions are not met. For example, rather than light, the oil may be heavy viscous oil and/or the reservoir may be substantially depleted of oil so that the reservoir pressure has been reduced. In such situations, it may be more difficult to recover oil from the reservoir. This leaves much residual oil trapped within the reservoir as an unrecoverable resource.
Figure 2 illustrates oil 230 wetting an outside surface of sand particles 210A-C and within two oil-filled pores 220A-B formed by the sand particles. Such oil wetting of sand may make substantial amounts of the reservoir oil difficult to recover due to strong attractions such as high surface tension forces and capillary forces holding them fixedly to such regions. It may be difficult to remove the oil from such regions by using pressure as the only driving force for removal. Additionally, when water is present external to the pores it may tend to hold the oil inside the pores.
Various enhanced oil recovery methods are known to improve oil recovery from a reservoir. Figure 3 illustrates a steam flooding enhanced oil recover operation to improve oil recovery from a reservoir. Steam addition system 310 comprising a steam generator, a stack gas scrubber, piping, flow control elements, and a steam injection line is used to add or inject steam into oil reservoir 320. The steam heats the oil in the reservoir to reduce the viscosity of the oil and make it less resistive to flow (similarly to the way that honey or molasses flows better when heated). This may allow hot oil proximate sand particle surfaces and within pores to become sufficiently mobile relative to the sand that the oil can move toward oil production well 330 suction inlet and be recovered from the reservoir at the wellhead.
There are several problems associated with steam flooding. A first problem is channeling wherein steam added to the reservoir takes the path of least resistance to the oil production well by improving the recovery of the weakest attached and most available oil first. Once a route to the oil production well has been established further steam flooding has decreased effectiveness due to the easy bypass to the low pressure oil production well. A second problem with steam flooding is that it is less favorable for deep oil reservoirs with high pressures. This is partly due to the increased pressure and heating needs to make the steam suitable for the high reservoir pressures.
Accordingly, there is a need for an improved approach for improving oil recovery from a reservoir.
BRIEF DESCRIPTION OF THE DRAWINGS
The features, aspects, and advantages of the invention will become more thoroughly apparent from the following detailed description, appended claims, and accompanying drawings in which:
Figure 1 illustrates an oil production well recovering oil from an oil reservoir.
Figure 2 illustrates difficult to recover oil.
Figure 3 illustrates a steam flooding enhanced oil recover operation to improve oil recovery from a reservoir.
Figure 4 illustrates a process flow for adding a recovery composition to an oil reservoir and then removing oil from the reservoir. Figure 5 illustrates a process flow for adding a recovery composition to a production well and then removing oil through the well.
Figure 6 illustrates a process flow for adding a recovery composition to a production well and using steam flooding.
Figure 7 illustrates a process flow for adding a recovery composition according to a cup tool method.
Figure 8 illustrates a process flow for adding a recovery composition to a steam well.
Figure 9 illustrates a schematic diagram for adding a recovery composition to an injection well.
Figure 10 illustrates a schematic diagram of improved recovery of difficult to recover oil with the use of a recovery composition.
Figure 11 illustrates a schematic top view of an exemplary oil reservoir field that was treated by an oil recovery composition, the top view showing positions of injection wells and recovery wells control sample of oil recovered from a control well of the exemplary oil reservoir shown in Figure 11, the control sample not affected by the oil recovery composition injected into the oil reservoir.
Figure 12 illustrates exemplary gas chromatograph data for a sample of oil taken from well R16 as a control sample.
Figure 13A illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well Rl of the oil reservoir shown in Figure 11.
Figure 13B illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R2 of the oil reservoir shown in Figure 11.
Figure 13C illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R3 of the oil reservoir shown in Figure 11.
Figure 13D illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R4 of the oil reservoir shown in Figure 11.
Figure 13E illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R5 of the oil reservoir shown in Figure 11.
Figure 13F illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R6 of the oil reservoir shown in Figure 11.
Figure 13G illustrates exemplary gas chromatograph data determined for an oil sample that was collected from well R8 of the oil reservoir shown in Figure 11. Figure 14 illustrates a system for washing oil-contaminated soil with an oil recovery composition.
DETAILED DESCRIPTION
Terminology
Before providing a detailed explanation of the claimed subject matter and various exemplary embodiments thereof, some terms that will be used throughout this description are briefly defined as follows:
"Oil" refers to an arbitrarily complex organic liquid mixture of naturally occurring hydrocarbon and other components having arbitrary and widely varying properties such as viscosity, density, color, and composition.
"Reservoir" refers to a subsurface region that contains oil. The reservoir may include a geologic formation or trap of oil wherein the oil is contained within voids and pores of sand, rock, shale, and similar structures. The reservoir may be a terrestrial reservoir or an off-shore reservoir.
"Viscosity" refers to an oil's resistance to flow.
"Density" refers to mass of oil per unit volume. Both viscosity and density affect the ability to get oil to flow to a well bore of a production line and the ability to pump the oil within the line. A high viscosity, high density oil may be more difficult to recover than a low viscosity, low density oil partly because the oil may become trapped within voids in the reservoir and may be difficult to remove from these voids. By way of analogy, it is similarly more difficult to pour honey through a small opening than it would be to pour water through the same opening.
"Permeability" refers to the fluid transmitting measure of a sand or rock material of a reservoir.
"Mobility" refers to the ratio of permeability to viscosity.
Additionally, unless indicated otherwise percentages for compositions are percentage by volume. For example, a composition having 95 percent (%) fatty acid alkyl ester may have 95 gallons of fatty acid alkyl ester for every 100 gallons of the composition. Oil Recovery Compositions
In one embodiment, a recovery composition is described. The recovery composition is suitable for introduction into a reservoir to improve the recovery of oil contained within the reservoir. In one embodiment, the recovery composition comprises at least one type of fatty acid alkyl ester. The recovery composition may contain a blend of different fatty acid alkyl esters. In the case of a blend, the different types of fatty acid alkyl esters may be in any proportion that is desired for the particular implementation.
Suitable fatty acid alkyl esters for a recovery composition may be represented by the general formula R'COOR wherein R' and R are typically different hydrocarbon groups containing carbon and hydrogen and potentially other components. For example, the groups may contain heteroatoms such as nitrogen, oxygen, sulfur, and others that may be found in organic compounds. The fatty acid alkyl ester may be an ester derived from a triglyceride. For example, the fatty acid alkyl ester may be a vegetable oil lower alkyl ester. The term "lower alkyl ester" refers to an alkyl ester having an R-group of between 1 and 5 carbons inclusive and preferably between 1 and 2 carbons inclusive. This may include such R-groups as methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, and isopentyl. Preferably the R-group contains 1 or 2 carbons. For example, the fatty acid alkyl ester may comprise a soy methyl ester or a soy ethyl ester. The R'-group may comprise a carbon chain having between 4 and 22 carbons. In one embodiment, the fatty acid alkyl ester is a "long-chain fatty acid alkyl ester" having an R'-group with between 12 and 20 carbons inclusive and preferably between 16 carbons or 18 carbons inclusive. The carbon chain may be saturated and contain no double bonds or be unsaturated and contain one or more double bonds. The fatty acid alkyl ester may comprise a mixture of sixteen carbon chain length methyl esters, seventeen carbon chain length methyl esters, and eighteen carbon chain length methyl esters. For example, the mixture may comprise a linoleic acid methyl ester, an oleic acid methyl ester, a stearic acid methyl ester, and a palmitic acid methyl ester.
Synthesis Of Fatty Acid Alkyl Esters By Trans-esterification Of Triglycerides
One method for creating a fatty acid alkyl ester suitable for use in a recovery composition is trans-esterification of a plant or animal triglyceride. Triglycerides are oils or lipids that occur naturally in plants and animals. The triglycerides are esters generally characterized by having three molecules of fatty acids linked to glycerol. Different types of triglycerides are contemplated including those present in natural oils of plants, vegetables, corn, spent French-fry oil, olive, palm, coconut, oleaginous seeds, soybean, rapeseed, sunflower, canola, safflower, animals, animal tallow, butter, milk, and others. Table 1 shows approximate fatty acid concentrations in triglycerides from exemplary plant and animal sources.
Table 1. Fatty Acids In Naturally Occurring Substances
Triglyceride Laurie3 & Palmitic0 Stearic" Oleic6 Linoleicf
Source Myristic"
Coconut 74 10 2 7 -
Corn - 8-12 3-4 19-49 34-62
Olive - 9 2 84 4
Palm - 39 4 40 8
Safflower - 6 3 13 78
Soybean - 9 6 20 52
Sunflower - 6 1 21 66
Beef 5 24-32 20-25 37-43 2-3
Milk - 25 12 33 3 n-Dodecanoic acid, CH3(CH2)10COOH, 12:0 n-Tetradecanoic acid, CH3(CH2)12COOH, 14:0 n-Hexadecanoic acid, CH3(CH2)14COOH, 16:0 n-Octadecanoic acid, CH3(CH2)16COOH, 18:0 cis-9-Hexadecenoic acid, 18:1(Δ9) cis,cis-9,12 Octadecadieoic acid, 18:2(Δ9 12)
Taking soybean oil as an example, soybean oil triglycerides contain a mixture of fatty acids having either 16 or 18 carbons and generally contain, in largest proportion, unsaturated 18 length carbon chains.
Trans-esterification is the process of reacting a triglyceride with an alcohol in the presence of a catalyst to produce an ester and glycerol. For example, soy oil may be trans-esterified with methanol in the presence of a suitable base catalyst such as potassium hydroxide to produce soy derived fatty acid methyl esters plus glycerol as follows:
Ol I3 + yiycoroi
(COPRODUCT) )
Figure imgf000007_0001
(SOY TR IGLYCERIDE) The esters may be recovered from the lighter liquid phase and purified as desired.
Certain fatty acid alkyl esters are commercially available. For example, soy methyl ester, which belongs to the fatty acid alkyl ester structural class, is commercially available from a number of sources including AG Environmental Products LLC (AEP) of Lenexa, Kansas who offer soy methyl ester under the tradename SoygoldR Marine. Soy methyl ester is also known as methyl soyate and biodiesel. Soy methyl ester has been assigned CAS Registry Number 67784-80-9. The SoygoldR Marine product comprises in significant proportion C16-C18 fatty acid methyl esters that are derived from soybean oil. Saturated fatty acid methyl esters contained in significant proportion in methyl soyate are methyl esters of lauric acid, palmitic acid, and stearic acid. Unsaturated fatty acid methyl esters contained in significant proportion in methyl soyate are methyl esters of oleic acid, linoleic acid, and linolenic acid. The product is a light yellow colored liquid that has a melting point of about -10°C (a liquid at room temperature), a normal boiling point greater than 200°C (typically 315°C), a vapor pressure typically less than about two millimeters mercury (mmHg) (non-volatile), a specific gravity of about 0.88 g/ml (lighter than water), and very low solubility in water at room temperature.
In addition to a fatty acid alkyl ester, one embodiment of a suitable recovery composition that may be used to improve oil recovery from a reservoir also includes a surfactant 520, a colloid, an acid 530, or some combination. In one embodiment, the concentration of the fatty acid alkyl ester may be between about 85% and about 99.89% or preferably between about 94% and about 98.99%. In this embodiment, the concentration of the surfactant may be between about 0.1% and about 10% or preferably between about 1% and about 5%. Finally, the concentration of the acid may be between about 0.01% and about 5% or preferably between about 0.01% and about 1%. For example, an exemplary concentration may comprise 96% soy methyl ester, 3% F-500™ surfactant (which will be discussed more fully below), and 1% vinegar (more than 4 percent aqueous solution of acetic acid).
Suitable surfactants for use in a recovery composition may be any surface active or interfacial agent that gets absorbed at an interface and changes the properties of the interface. For example, the surfactant may be an interfacial tension reducing agent that reduces the interfacial tension of a medium when it is added to the medium. Suitable surfactants may be selected from the group including but not limited to an amphipathic surfactants, anionic surfactant, cationic surfactants, detergents, and soaps. The surfactant may be soluble in the fatty acid alkyl ester composition. The surfactant may be thermally stable at reservoir conditions of temperature, pressure, salinity, and pH. The surfactant may also be comparatively non-toxic. The surfactant may be an amphipathic surfactant having both lyophilic and lyophobic groups. The surfactant may comprise a hydrophobe portion that prefers oil to water and a hydrophile portion that prefers water to oil. The surfactant may be an anionic surfactant that dissociates to yield a surfactant ion whose polar group is negatively charged. Exemplary anionic surfactants include sulfate surfactants (e.g., petroleum sulfates, alkyl sulfates, aryl sulfates), sulfonate surfactants (e.g., petroleum sulfonates, alkyl sulfonates, aryl sulfonates), and others. The surfactant may also be a cationic surfactant that dissociates to yield a surfactant ion whose polar group is positively charged. Exemplary cationic surfactants include alkylpyridinium salts and quaternary ammonium salts. The surfactant may also be a detergent formulation that contains other components.
According to one embodiment, the surfactant may be the F-500™ surfactant. F-500™ Dyna-Drill Foamer is a surfactant and foaming additive that is available from BCI Products, of Houston, Texas. This surfactant is commercially available, is comparatively non-toxic, is stable under and additionally may be useful to inhibit flammability of a material onto which it is applied.
According to another embodiment, the surfactant may be a soap made by treating a fatty acid with base to create a sodium or potassium salt of the fatty acid. For example, the surfactant may comprise a saponification product of a fatty acid similar to the fatty acid of the fatty acid alkyl ester. According to still another embodiment, the surfactant may comprise ARMOHIB® 31, ETHOMID® O/17, ETHOMID® HT/23, ETHOFAT® 18/24, ETHOFAT® 242/25, or ARMOHIB® 28, which are all available from Akzo Nobel Chemicals Ltd, of Arnhem the Netherlands, and having other places of business and sales offices. In particular, the surfactant may comprise a quaternary amine compound like ARMOHIB® 31, hydrogenated tallow amides like ETHOMID® HT/23, ethoxylated tall oil like ETHOFAT® 242/25, or fatty amines and alkoxylated fatty amines like ARMOHIB® 28. Depending upon the structure of the surfactant or mixture of surfactants selected, the surfactant may function as an emulsifier, dispersant, oil-wetter, water- wetter, foamer, defoamer or some combination to reduce interfacial tension and capillary forces of the oil within the voids. Surfactants may be costly such that the surfactant may be added to the composition in the smallest proportion that is found to be effective. Suitable surfactants are also preferably not diluted to any significant extent by water, since the water tends to settle out of the oil recovery composition. For example, the surfactant may come as a gel or similar highly viscous liquid.
An oil recovery composition may also include a colloid instead of or in addition to a surfactant. The term "colloid" will be used to refer to a heterogeneous mixture of a liquid and sufficiently small solid particles. The solid particles may be large enough to scatter a light beam but too small to settle out by gravity. The solid particles may be highly concentrated. Different solid particles are contemplated including inorganic solid particles (e.g., clays), organic solid particles (e.g., starches, polymers, etc.). The solid particles may be less than about 2 microns in diameter. A micelle emulsion is also contemplated wherein the solid particles are replaced by fatty acid soap micelles. Suitable colloids are preferably not diluted with water. The colloid may tend to disperse upon application and therefore aid in the distribution and in particular the lateral distribution of an oil recovery composition through an oil reservoir. For example, the colloid may react with water in a water table to draw the composition into and laterally through the water table from where it may percolate up into the oil reservoir. Accordingly, adding the colloid may encourage improved distribution of the composition within an oil reservoir. One colloid that is contemplated is the TWC210™ colloid, which is commercially available from the Ward Companies of Garden Grove, California.
Different colloid concentrations are contemplated for oil recovery. In one embodiment, a colloid-containing oil recovery composition may have a concentration of the fatty acid alkyl ester may be between about 65% and about 98.89% or preferably between about 78% and about 93.99%. In this embodiment, the concentration of the surfactant may be between about 0.1% and about 10% or preferably between about 1% and about 5%. The concentration of the colloid may be between about 1% and about 20% or preferably between about 5% and about 16%. Finally, the concentration of the acid may be between about 0.01% and about 5% or preferably between about 0.01% and about 1%. One contemplated colloid-containing oil recovery composition includes about 90% soy methyl ester, about 5% TWC210 colloid, about 3% essentially undiluted F-500™ surfactant, and about 2% vinegar (dilute acetic acid solution). Another contemplated colloid-containing oil recovery composition includes about 80% soy methyl ester, about 16% TWC210 colloid, about 2% essentially undiluted F-500™ surfactant, and about 2% vinegar.
The colloid may be provided in addition to the surfactant, as a partial replacement or substitute for the surfactant, or as a complete replacement of the surfactant in the recovery composition. In one embodiment each amount of surfactant is substituted or replaced by multiple amounts of a colloid. For example, each 1% reduction in surfactant concentration may be accompanied by between about a 1% to 10% or about a 3% to 8% increase in colloid concentration.
An acid may be added to the oil recovery composition to aid in suspension of the surfactant, the colloids, or both the surfactant and the colloid in the fatty acid alkyl ester. Suitable acids for the recovery composition may comprise weak acids that do not completely disassociate in water, strong acids that essentially completely dissociate in water, or both a weak acid and a strong acid. Weak acids that are contemplated include an organic acid, carboxylic acid, acetic acid, vinegar comprising about 5% acetic acid in water, formic acid, citric acid, lemon juice, butyric acid, benzoic acid, carbonic acid. Preferably the acid comprises acetic acid in the form of vinegar. Strong acids that are contemplated include an inorganic acid, a mineral acid, sulfuric acid, hydrochloric acid, nitric acid, perchloric acid, and others.
Preparation of the composition may include adding desired proportions of the surfactant and/or the colloid, and the acid to the fatty acid alkyl ester followed by mixing as desired. In one embodiment, it may be desirable to vigorously mix the composition sufficient to emulsify the acid, which may include an aqueous solution of acid such as vinegar, into the fatty acid alkyl ester, to avoid rapid phase separation, which may decrease the effectiveness of the composition.
Adding Compositions To Oil Reservoirs To Aid Recovery
The compositions described above are effective for improving recovery of oil from reservoirs. Figure 4 illustrates a method 400 for recovering or removing oil from an oil reservoir, according to one embodiment. The method commences at block 401, and then proceeds to block 410, where an effective amount of a recovery composition such as described above is added to an oil reservoir. This may include adding between about 300 gallons and about 3,000 gallons or between about 500 gallons and 1500 gallons per well of a recovery composition. As described above, the composition may contain the fatty acid alkyl ester (e.g., a vegetable derived fatty acid methyl ester) at a concentration between about 85% and about 99.89%, a surfactant at a concentration between about 0.1% and about 10% (e.g., F-500), and an acid at a concentration between about 0.01% and about 5% (e.g., acetic acid or citric acid). Alternatively, the composition may be another composition described herein or one that would be apparent to a person having an ordinary level of skill in the art and the benefit of the present disclosure.
The recovery composition may affect the oil in the reservoir and in particular may make it easier to recover the oil from the reservoir. It is believed the recovery composition reduces attractions between the oil and the oil containing structures, such as surface tensions, capillary attractions, and physical or chemical bonds between oil and sand. This may make the oil more mobile relative to the sand and rock.
The method advances from block 410 to block 420 where oil is removed from the oil reservoir. Advantageously, as a result of the recovery composition being introduced, it may be possible to remove more oil for a longer period of time than would have been possible if the recovery composition had not been applied. Experimental studies have demonstrated increased oil production for several weeks and even several months at which time the reservoir may be re-treated with the recovery composition. The recovery composition described herein is particularly effective in this regard in comparison to prior art stimulants, because it is believed the recovery composition tends to disperse out into the reservoir with the same effect more effectively than prior art composition. Additional advantages include the fact that the composition is benign relative to production and refining and does not need to be removed from the recovered oil prior to refining. In fact, the composition may aid in cleaning or defouling production and refining lines. Additionally, since some fatty acid alkyl esters such as soy methyl ester may be added as a diesel additive, the composition may be recovered during refining to serve a second purpose as an additive and thereby provide both an enhanced oil recovery benefit and also serve as an additive to refining products. The method terminates at block 430. Different methods presented below are contemplated for implementing the addition of recovery compositions as a liquid (or in a substantially liquid state) to oil reservoirs. Figure 5 illustrates a first embodiment wherein the composition is added via a production well. This embodiment may be useful when a steam line is not present and, in addition to improving oil recovery from the well, may assist in cleaning the production well, associated piping, and a region of the reservoir proximate the production well suction zone. Figure 6 illustrates a second embodiment wherein the composition is added to a production well and then steam is added to the production well. The steam may assist with distributing the composition to the reservoir, speeding the affect of the composition by decreasing viscosity, and thermally stimulating the oil and composition near the production line. Figure 7 illustrates a third embodiment wherein the composition is added to a well via a cup tool. This embodiment may be useful when the well becomes clogged or fouled and when the oil reservoir has a high water aquifer. Figure 8 illustrates a fourth method wherein the composition is added via a steam line associated with a production well or wells. This embodiment may be useful for reducing viscosity and increasing mobility of heavy oils and may additionally assist with cleaning the steam well. Other methods are contemplated.
Adding Compositions To Production Wells
Figure 5 illustrates a method 500 for recovering or removing oil from an oil reservoir by adding a recovery composition such as described above to a production well, according to one embodiment. The method commences at block 501, and then proceeds to block 510, where a production well is shut down. After shutting down the production well, at block 520 a recovery composition such as described above is added to the oil reservoir by way of the production well (e.g., added down the casing and preferably down the tubing within the casing). The method advances from block 520 to block 530 where the recovery composition is allowed to take affect on the reservoir for a period between about one day and about seven days. After the recovery composition has taken the desired affect on the reservoir at block 540 the production well is started up again and oil is removed from the oil reservoir. The method terminates at block 550. Adding Compositions To Production Wells With Steam Injection
Figure 6 illustrates a method 600 for recovering or removing oil from an oil reservoir by adding a recovery composition such as described above to a production well, according to another embodiment. The method commences at block 601, and then proceeds to block 610, where the production well is shut down. After the production well has been shut down, at block 620 a recovery composition is added to the oil reservoir by way of the production well. The recovery composition may be added down the casing or preferably down the tubing.
The method advances from block 620 to block 630 where an effective amount of steam is added to the oil reservoir by way of the production well. The effective amount may be an amount sufficient to flush the composition from the line into the reservoir and assist with dispersing the composition into the reservoir. A larger effective amount may also be used to thermally stimulate the oil within the reservoir by heating it to reduce its viscosity. Both of these amounts may depend upon the particular characteristics of the oil field including depth and the oil including viscosity. Accordingly, the amount of steam added may vary from a trivial amount sufficient to flush the line and disperse the composition from the line into the reservoir to a larger conventional amount to thermally stimulate the reservoir. Similarly, characteristics of the steam such as pressure and temperature may vary depending upon depth according to convention.
After the desired amount of steam has been added the steam addition may be stopped so that oil recovery may begin. The method advances from block 630 to block 640 where the production well is started up and oil is removed from the oil reservoir. The method terminates at block 650.
Adding Compositions Via Cup Tool
Figure 7 illustrates a method 700 for recovering oil from an oil reservoir by adding a recovery composition such as described above to a well with a cup tool, according to one embodiment. The method commences at block 701, and then proceeds to block 710, where a well is shut down. After the well has been shut down, at block 1020 a predetermined volume of a recovery composition is added to a cavity or chamber of the cup tool. The method advances from block 720 to block 730 where the cup tool is inserted into the well and the composition is released from the chamber. This may include inserting the cup tool chamber into proximate alignment with perforations in a perforated lining of the well and pressurized blowing the composition from the chamber with sufficient force to inject the composition into the reservoir and to remove oil structures that clog the lining at a particular perforation. Advantageously, the cup tool may assist with targeted distribution and dispersal of the composition and may additionally assist with cleaning deposits from the well. After releasing the composition, at block 740 the cup tool is removed from the well. The method advances from block 740 to block 750 where oil is recovered from the oil reservoir. The method terminates at block 760.
Adding Compositions To Steam Lines
Figure 8 illustrates a method 800 for recovering or removing oil from an oil reservoir by adding a recovery composition such as described above to a steam line, according to one embodiment. The method commences at block 801, and then proceeds to block 810, where the steam line is shut down. After the steam line has been shut down, at block 820 a recovery composition is added to the oil reservoir by way of the steam line. The method advances from block 820 to block 830 where steam is added to the oil reservoir by way of the steam line to increase the effectiveness of the recovery composition at oil recovery. After adding an effective amount of the steam, at block 840 oil is removed from the oil reservoir. As desired, oil may be continuously recovered from the reservoir concurrently with addition of recovery composition at block 820, addition of steam at block 830, or both. The method terminates at block 850.
An additional advantage with injecting a recovery composition such as described above is steam well cleaning. Conventionally such steam wells are known to foul with hydrocarbons. This may cause flow restriction or steam dispersal and may limit the amount of steam that can be effectively delivered to the reservoir. One prior art approach for remedying this problem is to inject strong acids into the steam well to remove the hydrocarbons. However this approach has the disadvantage of introducing foreign acids into the oil which may cause corrosion of subsequent petroleum refining equipment or which may need to be separated from the oil prior to the petroleum refining processing. Accordingly, cleaning with fatty acid alkyl compositions, which do not cause corrosion during refining, provides an attractive alternative approach. Advantageously, this may allow both cleaning or defouling of the steam well, which may make steam stimulation more effective, as well as concurrently providing the composition to the reservoir to enhance oil recovery. This approach may additionally clean other processing equipment such as pumps that pump the oil from the reservoir and piping which may both be fouled by oil components such as paraffins.
Other Methods Are Contemplated
Those having an ordinary level of skill in the art and the benefit of the disclosure will appreciate that other methods for adding recovery compositions such as described above to oil reservoirs are contemplated. For example, according to yet another method, a recovery composition may be added via a water injection well and then chased with water. The chase water may be provided in amount sufficient to disperse the composition as well as pressurize the well and mobilize the oil. Still another method includes adding a sufficient amount of the recovery composition as part of a fracing procedure (e.g., prior to pressurizing).
Detailed Working Example
Figure 9 illustrates an example application of a soy methyl ester oil recovery composition to an oil reservoir, according to one embodiment. Initially a scrapper tool is inserted into an injection well 950 to open and clear the injection well. Then the scrapper tool is removed and an injection tool is inserted into the injection well. Water 935 from a separation tank 925 is added to the reservoir 960 via a pump 920. A check valve 945 opens when the pump discharge reaches about 200 psi. This valve may essentially suppress flow from the reservoir. Recovery composition 910 may be added to the injection well from a tanker truck 905 via a pump 915. This may include adding about 100 gallons or more (e.g., as much as 500 gallons or more) of recovery composition to the reservoir. Then water 935 may be added to push the recovery composition out of the well and into the oil reservoir as shown at 980. This may include adding between about 1 and about 50 times as much water as recovery composition, or more. Generally, the more water available for addition the better since the water aids in dispersing the composition into the reservoir by force of injection, percolation, and other mechanisms. Other segments may be added and these steps repeated as shown at 985 and 990 to vertically disperse the recovery composition along the oil reservoir. Desirably the composition may be dispersed along the oil containing region 970 of the reservoir instead of the gas containing region 965 or water containing region 975. In one embodiment, a plurality of segments each having a length between about 10 and about 50 feet are used to disperse the recovery composition over a substantial portion of the oil containing regions 970 of the reservoir. Advantageously, the recovery composition tends to improve recovery of the oil by weakening attachments between the oil and oil containing structures (e.g., sand, rock, shale, etc.). Oil may be recovered from the reservoir via a production well 955 and provided to the separation tank. In the separation tank the produced oil may separate into oil 930, water 935, and solids 940. The oil may be sent to refining and the solids to treatment/disposal.
Conceptualized Representation Of Improved Oil Recovery
Figure 10 illustrates a recovery composition such as described above interacting with oil wetting sand, according to one embodiment. Sand 1010 is shown having an oil wetted thereto, the oil containing at least some of a recovery composition dissolved therein. A water flood 1030 is coupled with the oil 1020 to remove the oil from the sand. The water flood 1030 may be replaced by another motive fluid or by steam.
The sand and the oil meet at an oil-sand interface. Near the interface are an acid (A), a surfactant (S), and a fatty acid alkyl ester (R-O-R') of a recovery composition dissolved in the oil. It is believed that one or more of these composition components act as interfacial agents to reduce attractions and adhesions between the oil and the sand. This is conceptually represented as a dashed line 1070. Advantageously, this tends to make it easier to recover substantial portions of the oil.
The oil and the water flood meet at an oil-water interface. Near the oil-water interface are an acid, a surfactant, and a fatty acid alkyl ester of the dissolved recovery composition. One or more of these components may act as interfacial agents to reduce interfacial tension between the oil and the water. This is conceptually represented as a dashed line 1060. As shown, a portion 1050A containing some of the recovery composition may be dislodged and carried away typically as a droplet of oil 1050B dispersed in the water flood. In such a way the recovery composition may be used to improve recovery of oil. Analysis Of Oil Recovered From A Reservoir Treated With An Oil Recovery Composition
Figure 11 illustrates a top view of an exemplary oil reservoir field 1100 that was treated by an oil recovery composition of the present invention. The top view shows the positions of steam injection wells (II, 12, 13, and 14) and recovery wells (Rl, R2, R3, R4, R5, R6, R8, and control recovery well R16).
Recovery compositions containing about 96% soy methyl ester, about 3% F- 500 surfactant, and about 1% vinegar were injected into the steam injection wells before oil samples were recovered from the recovery wells over approximately a three week period. In particular, injection well II was injected with 6700 gallons of recovery composition on a first date and five days later with an addition 5,300 gallons of the recovery composition; injection well 12 was injected with 7000 gallons of composition; injection well 13 was injected with 6000 gallons of the recovery composition and 6000 additional gallons of the recovery composition a day later; and injection well 14 was injected with 12000 gallons of the recovery composition. After injection of the compositions, steam was added to each of the injection wells to flush the composition from the lines and disperse the composition into the oil reservoir.
About four months after the first injection date, oil samples were recovered from each of the recovery wells and tested by gas chromatography. The oil sample collected from control recovery well R16 was not affected by the addition of the composition to the reservoir and serves as a control or benchmark for observing affects on the other oil samples due to addition of the composition.
Figure 12 illustrates gas chromatographic data determined for the control sample and Figures 13A-13G show gas chromatographic data determined for samples from wells Rl, R2, R3, R4, R5, R6, and R8, respectively. The gas chromatography data is an analytical representation of the different organic components in each oil sample. In particular, the position, shape, curvature, and roughness of the gas chromatography data line characterizes and represents the chemical composition of the oil sample. In this way the data acts as a fingerprint for the oil sample. In the absence of any affect by the composition, the gas chromatography data for each collected sample would be expected to be substantially identical within proximate oil wells on the same oil reservoir (i.e., similar to Figure 12). Comparison of the control sample shown in Figure 12 with the non-control samples in Figures 13A-13G show a different result. Firstly, this data shows that the composition added to the reservoir has affected and altered the chemistry of oil samples recovered from recovery wells several hundred feet from an injection well. Accordingly, the compositions and methods described herein have been effective to disperse the composition over an effective distance of an oil reservoir. Secondly, this data shows that the composition has been effective in altering the oil chemistry and chemical properties. This is believed to be partly due to the fact that the composition has made previously unrecoverable viscous oil available and present in the sample, and partly due to the fact that the composition may react with certain oil components to change them chemically. Such changes are believed to aid in recovery of oil from the oil reservoir.
Alternate Uses Of The Composition
The recovery compositions described herein have other uses. Several alternative uses are described below. Those having an ordinary level of skill in the art and the benefit of the disclosure will appreciate that still other uses are contemplated.
Cleaning Agent To Clean Oil Contaminated Soil
According to a first alternate embodiment, a recovery composition such as those described herein may be used to clean soil that is contaminated with oil. The recovery composition may assist with releasing the oil from the soil by weakening the physical and chemical attractions and attachments between the oil and the soil.
Figure 14 illustrates a two-stage contaminated oil cleaning system 1400, according to one embodiment. The two-stage system includes a primary treatment vessel 1425 and a secondary treatment vessel 1445. The vessels may be enclosed processing tanks having design specifications consistent with the uses and conditions described below.
Soil contaminated with oil is added to the primary vessel via a soil hopper 1405. Water and a soil-washing composition are mixed and added to the primary vessel via a water inlet 1410. The water is pressurized water and may be heated between about 100°F to about 200°F or between about 110°F and about 130°F. Enough water may be added to provide a good flush of the soil through and from the system including the vessels. The composition may be added in a ratio to the soil of about 0.01 to about 10 or between about 0.1 and about 2. The composition may comprise 80(±6)% soy methyl ester, 18(±5)% TWC210 or similar colloid, and 2(±1)% vinegar. Alternatively, other compositions described herein may be used instead. The primary vessel may be an elongated vessel having a long side along which the soil may travel from an entrance end at the inlets to an opposite end. The water inlet and hopper may be located on or proximate the entrance side. The water inlet and the hopper may additionally be located proximate one another towards a top of the primary vessel and aligned so that the water directs and mixes the soil downward due to its velocity.
Compressed air may be added to the primary vessel via an air inlet 1415. The air may be added in an amount sufficient to agitate the primary vessel contents including enough to mix the soil and the water-composition mixture. The air inlet may direct the air in a direction along a longest side of the vessel so as to encourage the water and soil in the tank to move in this direction. According to one embodiment at least some of the air is added upward along the length of the bottom of the vessel to encourage soil not to settle and pack, which may decrease the washing efficiency. Spent air may exit the vessel through a spent air treatment system 1420, which may include a venturi and air scrubber.
The soil and water move across the tank, from the entrance at the left to an exit at the right, and is removed from the primary vessel by a pumping system 1430. The primary vessel may have a size sufficient to provide an effective residence time for the composition and water to wash the soil. The residence time may be between about 1 minute and 5 hours or preferably between about 5 minutes and 1 hour. The water and the soil washing composition loosen and remove an effective amount of the oil from the soil. The removed oil and the composition may separate from the water as droplets within the water and may rise to an oil layer at the top of the primary vessel. According to one embodiment, this layer is skimmed, pumped, or otherwise removed from the primary vessel for further processing.
A pumping system 1430 pumps the soil and water to a secondary treatment vessel 1445. The pumping system may comprise a gravel pump. The secondary vessel may be substantially as described for the primary vessel or may be different as desired. The soil mixture may enter the secondary vessel at a left hand entrance (as viewed) and travel from left to right along a longest length of the vessel to an exit side at the left. Water may be added via a water inlet 1440 to assist with movement of the soil and air may be added via an air inlet 1435 to assist with agitation of the vessel contents. The spent air may leave through a spent air treatment system 1450. Phase separated oil and composition may be skimmed and recovered from the secondary vessel or pumped out with the water for subsequent processing and recovery.
A pumping system 1455 removes water and soil from the secondary vessel at an opposite side from its inlet and pumps it to a dewatering system 1460. The dewatering system may comprise a dewatering means such as a large settling tank, shaker pit to shake out solids, a centrifuge, or some combination.
Spill Control Agent To Treat Oil Spills
According to a second alternate embodiment, the recovery composition describe herein may be used as oil spill agent to recover or remove oil from an oil spill. The recovery composition may be used to coat surfaces before contacted with the oil spill or to weaken bonds between oil and surfaces after they have been coated with oil.
A first method for recovering or removing oil from an oil spill may include: (1) spraying or otherwise applying an effective amount (e.g., between about 0.01-1 gallon per square foot or preferably about 0.1 gallons per square foot depending upon the amount of oil) of the recovery composition on environmental surfaces (e.g., rocks, sand, beaches, piers, boat docks, etc) that have been coated by oil from a spill, (2) allowing sufficient time for the composition to loosen the bonds between the oil and the soil (e.g., between about one minute and one day or preferably between about 0.5-2 hours, (4) spraying water on the soil to remove the oil from the soil, (5) collecting the removed oil, and (6) repeating (l)-(5) zero or more times until the oil has been removed to a desired extent.
A second method may include spraying or otherwise applying the recovery composition on surfaces before they are coated with oil to make the surfaces less susceptible to strong coating attachment by the oil. For example, following an oil spill on the sea a proximate beach may be sprayed with an effective amount of the recovery composition (e.g., about 0.1 gallons per square foot) before the oil spill reaches the beach to prevent the approaching oil spill from adhering strongly to the surfaces. Advantageously, this may reduce the impact of the spill as well as making remediation easier and less costly. The exemplary composition mentioned above for cleaning oil contaminated soil is also contemplated to be useful for this embodiment. Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
Clarifying Agent To Improve Solids Separation
According to a third alternate embodiment, the recovery composition described herein may be used to improve separation of solids from oil and water. For example, the recovery composition may be added to production oil or water pumped from the well to release solids suspended by the oil or water by weakening the attractions between the solids and the fluids. The recovery composition may reduce bonding between the solids and the fluids and allow them to separate by gravity. This may allow the oil and water to pass though to the production process with significantly reduced solids. Advantageously, this may reduce wear to processing equipment such as pumps and valves. This may also allow the solids to be recovered cleaner from knockouts and tanks than is possible by current methods involving polymers. Advantageously, such cleaner solids may be considered less hazardous materials for purposes of disposal, storage, or treatment.
A method for improving solids separation with the recovery composition may include: (1) adding an effective amount of a recovery composition, e.g., between about 0.01-0.1 gallons per gallon of fluid, to a process fluid (e.g., oil or water pumped from the well), (2) allowing sufficient contact (e.g., sufficient mixing within a valve or sufficient time within a tank or other high residence time equipment) to allow the recovery composition to contact the suspended solids, (3) allowing sufficient time for the composition to loosen the bonds between the oil and the soil and for the suspended solids to settle (e.g., between about one minute and one day or preferably between about five minutes and one hour depending upon the size of the density and size of the solids and the viscosity of the oil, and (4) conventionally processing the separated fluids and solids.
An example recovery composition that is contemplated to be useful for this embodiment includes 90(±5)% soy methyl ester and 10(±5)% TWC210 colloid. Acid may not be needed to provide suspension of the colloid since the composition may remain thoroughly mixed by flow, pumping, and similar means. Additionally, the composition may remain mobile rather than stagnant, which would promote separation. Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
Cleaning Agent To Remove Organic Fouling
According to a fourth alternate embodiment, the recovery composition may be used as a cleaning agent to remove oil component fouling from oil processing equipment. The recovery composition may also be used to clean the inside or outside of oil processing equipment such as knock out tanks, storage tanks, production lines, pipes, valves, pumps, and other processing equipment in order to remove oil component fouling such as organic residue, hydrocarbon fouling, or cake. Advantageously, the recovery composition may be more compatible with the refining process than other cleaning agents such as acids. The composition and in particular the surfactants may also aid in reducing H2S levels.
A method for removing oil component fouling from an evacuated tank (e.g., a knock out tank or oil storage tank) may include: (1) spraying or otherwise applying an amount of the recovery composition sufficient to coat the surface of the tank (e.g., typically less than about 0.01 gallons per square foot of tank, (2) allowing sufficient time for the composition to loosen the bonds between the fouling and the tank (e.g., between about 1 minute and 1 day or preferably between about 0.5-2 hours, (4) spraying water preferably a high pressure stream of water on the tank to remove the fouling and the recovery composition from the tank, (5) disposing of the removed fouling and composition, and (6) repeating (l)-(5) zero or more times until the tank has been cleaned to a desired extent.
A method for removing fouling from less accessible processing equipment such as production lines, pumps, and valves is also contemplated. Depending upon the particular implementation pure composition or solutions (e.g., diluted with water) of the recovery composition may be circulated through the processing equipment. Advantageously, this may be used to remove oil fouling such as paraffin and asphalt deposits from such inaccessible processing equipment.
An example recovery composition that is contemplated to be useful for this embodiment includes 80(±8)% soy methyl ester, 5(+2)% F-500 surfactant, 13(±5)% TWC210 colloid, 2(±1)% vinegar. Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
Graffiti Cleaning Agent To Remove Graffiti
According to a sixth alternate embodiment, a similar recovery composition and method as described above to remove fouling may be used to remove oil-based paint or graffiti from surfaces. A similar recovery composition may also be used to remove oil components from cement, such as parking garage floors.
Bio-Compatible Cleaning Agent For Oil Coated Wildlife
According to a fifth alternate embodiment, the recovery composition may be used to clean wildlife such as birds and animals that are contaminated by oil, such as by an accidental oil spill. The recovery composition may weaken the bonds between feathers, fur, and skin and the oil. Advantageously, this may reduce the impact of the spill on the wildlife and may allow cleaning the wildlife with a non-toxic, non- irritating, and biodegradable agent.
A method for cleaning wildlife may include: (1) restraining the wildlife such as by hand or within a cage, (2) spraying or otherwise applying an amount of the recovery composition sufficient to coat the surface of the wildlife (e.g., less than about one gallon or preferably less than about 0.1 gallon per animal the size of a normal ptarmigan), (3) massaging the recovery composition into contact with the animals fur or features, (4) allowing sufficient time for the composition to loosen the bonds between the oil and the fur or feathers (e.g., between about thirty seconds and about one hour or preferably less than about ten minutes, (5) gently spraying water on the wildlife to remove the oil and the recovery composition from the fur or feathers, and (6) repeating (2)-(5) zero or more times until the wildlife has been cleaned to a desired extent.
An example composition that is contemplated to be useful for this embodiment includes 90(±5)% soy methyl ester, 8(±4)% lanoline, and 2(±1)% aloe vera. These components and concentrations may be replaced with other non-toxic and non-irritating components and concentrations. For example, the lanoline may be replaced by another surfactant used in cleaning agents for humans such as bath soaps, shampoos, and cleaners that are sufficiently mild for humans. Other compositions and methods are contemplated and will be apparent to a person having an ordinary level of skill in the art and the teachings of the present disclosure.
Demulsifying Agent For Oil-Water Emulsions
According to a sixth alternate embodiment, the recovery composition may be used to remove water from oil by breaking an oil-water emulsion. Oil recovered from reservoirs often contains oil-water emulsions. An emulsion is a liquid mixture of two or more liquid substances that are not normally dissolved in one another. One liquid is held in suspension in the other liquid. In the water-in-oil emulsion the water is the suspended minority liquid and oil is the suspending majority liquid. The amount of water may depend upon the chemical characteristics of the oil and how it is produced. Many oils contain emulsifying agents. Exemplary emulsifying agents include solid particles (e.g., silt, drilling mud, or clay particles), naturally occurring surfactants, and certain chemicals that may be added during production (e.g., corrosion inhibitors, scale controllers, paraffin controllers, and the like). The water, the oil, and any emulsifying agents that are present may become intimately mixed and emulsified during turbulent mixing and shearing processes that occur in pumps, valves, pipes, and other production equipment.
These oil-water emulsions may contribute to numerous problems during transport in pipelines and during refining. One problem is that the water may contain corrosive materials (e.g., salts, acids, etc.) that may damage pipelines and refining equipment. Another problem is that the water constitutes additional fluid that needs to be transported and refined, which increases the costs. Yet another problem is that the emulsions have high viscosity, which may lead to pumping problems, and may accumulate on separators, leading potentially to dangerous conditions and costly, labor intensive production shutdowns. Due to these problems, and others, many pipeline companies, and refining companies, have set specifications, often known as BS&W (bottom sediment and water) specifications, which limit the amount of water in the oil for purposes of transport via pipeline or refining. The oil is often tested, for example with a BS&W monitor which detects entrained water content in oil due to the water changing the capacitive reactance as a function of the dielectric constant, and additional costs may be imposed, or services refused, if the water content is higher than specified. The stability of the emulsion depends upon the characteristics of the oil and water, and the way in which they are mixed. Given sufficient time, most emulsions will break. However, prolonged processing times are generally not desirable in commercial oil production. In order to reduce the amount of water present in the oil, chemicals known as emulsion breakers are often added to the oil to destabilize or break the oil- water emulsions and encourage gravimetric separation of the water from the oil, in which it was mixed, based on differences in density. This process is known as chemical demulsification. Existing chemicals have a number of limitations and there is a general need in the art for new demulsification compositions.
A method for demulsifying an oil-water emulsion, according to an embodiment, may include adding a composition containing a fatty acid alkyl ester, a surfactant, and an acid, to the oil-water emulsion to thereby form a mixture, and permitting a phase separation to occur within said mixture to thereby produce an oil phase and a water phase. At least a portion of the resulting oil phase may be processed and at least a portion of the resulting water phase may be disposed. In one aspect, the demulsification may be practiced offshore and the at least a portion of the separated water disposed offshore. Embodiments of compositions and methods may help oil producers meet water content specifications set for pipelines and refineries, and in general may help to reduce equipment corrosion, processing costs, downtime, and other problems associated with the water.
Various compositions described herein are suitable for breaking oil-water emulsions. In one embodiment, the composition may comprise a concentration of the fatty acid alkyl ester that may be between about 85% and about 99.89%, the concentration of the surfactant may be between about 0.1% and about 10%, and the concentration of the acid may be between about 0.01% and about 5%. In another embodiment of the invention, the concentration of the fatty acid alkyl ester, such as soy methyl ester, may be at least about 85%, the concentration of the surfactant, such as TWC210 colloid or F-500™ surfactant or some combination, may be between about 4% and about 7%, and the concentration of the acid, such as vinegar, similarly dilute weak organic acid solution, or other similarly dilute acid solution, may be between about 1% and about 1.5%. Such compositions achieve a rapid separation of the water from the oil, essentially break the entire emulsion, provide a sharp interface between a lower oil phase and an upper water phase, and provide a substantially pure water phase. The relative proportions of fatty acid alkyl ester, surfactant, and acid, may be customized, at least to some extent, based on the nature of an oil-water emulsion for a particular reservoir or field.
Often, a pump or metering device may be used to add the composition to the emulsion. Alternatively, the composition may be added manually. The composition may be added to the emulsion in a phase separation vessel, such as a tank, or at the inlet piping to the vessel. Often, a vessel may be favored because it may have a size that facilitates gravity settling of water droplets from the oil. Of course the vessel is not required and the composition may also be added to an emulsion flowing through a pipe or pipeline without the vessel. The composition may be mixed with the emulsion to give a concentration of the composition in the range of approximately 1-1000 ppm (parts per million). Higher concentrations may also be used. The method may further include mixing the composition with the emulsion. The mixing may be achieved by using an agitator, such as a motorized stirrer with a plurality of mixing blades, or by circulating the mixture through a pipe, elbow, valve, pump, or similar mixing device.
Accordingly, embodiments of the composition and method for demulsifying an oil-water emulsion resulting from the production of crude oil from a subsurface crude oil reservoir. The ability to remove water from oil by such methods may be of great assistance and economic benefit to oil producers in helping them meet water content specifications for pipelines and refineries and in general reducing the problems associated with oil-water emulsions.
In the foregoing specification, the invention has been described with reference to specific embodiments thereof. It will, however, be evident that various modifications and changes may be made thereto without departing from the broader spirit and scope of the invention. The specification and drawings are, accordingly, to be regarded in an illustrative rather than a restrictive sense.

Claims

CLAIMSWhat is claimed is:
1. A composition comprising, a fatty acid alkyl ester; a surfactant; and an acid.
2. The composition of claim 1, wherein the concentration of the fatty acid alkyl ester is between about 85 percent and about 99.89 percent; wherein the concentration of the surfactant is between about 0.1 percent and about 10 percent; and wherein the concentration of the acid is between about 0.01 percent and about 5 percent.
3. The composition of claim 1, wherein the concentration of the fatty acid alkyl ester is between about 94 percent and about 98.99 percent; wherein the concentration of the surfactant is between about 1 percent and about 5 percent; and wherein the concentration of the acid is between about 0.01 percent and about 1 percent.
4. The composition of claim 1 , wherein the fatty acid alkyl ester comprises a fatty acid alkyl ester that is selected from the group consisting of a methyl ester derived from a vegetable triglyceride, an ethyl ester derived from a vegetable triglyceride, and a propyl ester derived from a vegetable triglyceride; and wherein the acid comprises a solution containing a carboxylic acid and water.
5. The composition of claim 1 : wherein the fatty acid alkyl ester comprises an ester that is selected from the group consisting of: a soy methyl ester, a soy ethyl ester, and a soy propyl ester; wherein the surfactant comprises a surfactant that is selected from the group consisting of a drilling foaming additive, F-500, and TWC210; and wherein the acid comprises vinegar.
6. The composition of claim 1, wherein the fatty acid alkyl ester comprises a mixture of sixteen carbon chain length methyl esters, seventeen carbon chain length methyl esters, and eighteen carbon chain length methyl esters.
7. The composition of claim 6, wherein the mixture comprises linoleic acid, oleic acid, stearic acid, and palmitic acid.
8. A method for recovering oil from a reservoir comprising: adding the composition of any one of claims 1 to 5 to an oil reservoir and recovering oil from the oil reservoir.
9. A method for breaking an oil-water emulsion comprising: adding the composition of claim 2 to the oil-water emulsion to thereby form a mixture and permitting a phase separation to occur to thereby produce an oil phase and a water phase.
10. A method for cleaning oil contaminated soil comprising: mixing the composition of claim 2 with water to form a mixture, contacting the mixture with the oil contaminated soil in a vessel at a temperature in the range of 100- 200°F, wherein the ratio of the composition in the mixture to the soil is in the range of approximately 0.01-10, permitting the oil to separate from the soil as an oily phase at the top of the water, and removing the oily phase from the vessel.
11. A method comprising: applying in the range of 0.001-1 gallons per square foot of the composition of claim 1 to a environmental surface, either before or after the surface is coated with oil from an oil spill, spraying water on the environmental surface having the applied composition after the surface is coated with the oil from the oil spill to remove the oil, and collecting the removed oil.
12. A method comprising: adding an effective amount of recovery composition comprising a fatty acid alkyl ester, a surfactant, and an acid to an oil reservoir; and removing oil from the oil reservoir.
13. The method of claim 12, wherein adding the recovery composition comprises adding between 300 to 3,000 gallons of the composition to the oil reservoir, the composition containing between 0.1-10 percent surfactant, containing between 0.01-5 percent weak acid, and at least about 85 percent plant derived fatty acid alkyl ester to the oil reservoir.
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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1961799A1 (en) * 2007-02-20 2008-08-27 BIOeCON International Holding N.V. Process for reducing the viscosity of highly viscous hydrocarbon mixtures
GB2432177B (en) * 2004-11-10 2009-05-06 Bj Services Co Method of treating an oil or gas well with biodegradable low toxicity fluid system
EP2059578A2 (en) * 2006-09-08 2009-05-20 Marathon Oil Canada Corporation Biodiesel production and use in oil sands processing
CN102977872A (en) * 2012-11-29 2013-03-20 辽宁石油化工大学 Enhanced foam oil-displacing agent for improving oil recovery rate in tertiary oil recovery, and preparation method thereof
EP3194358A4 (en) * 2014-09-15 2018-02-14 Elevance Renewable Sciences, Inc. Low-toxicity olefinic ester compositions and methods of using the same
WO2018178402A3 (en) * 2017-03-31 2018-12-27 Oiliq Intelligent Solutions Gmbh Composition for reducing the viscosity of crude oil and crude oil residues as well as for loosening and separating crude oil and/or crude oil residues from other liquid and/or solid substances
CN109294548A (en) * 2018-11-29 2019-02-01 西安长庆化工集团有限公司 A kind of ageing oil low-temperature demulsification thinner and its preparation method and application

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6806233B2 (en) * 1996-08-02 2004-10-19 M-I Llc Methods of using reversible phase oil based drilling fluid
US7191834B2 (en) * 2004-09-22 2007-03-20 Halliburton Energy Services, Inc. Foamed cement compositions and associated methods of use
US7231976B2 (en) * 2004-11-10 2007-06-19 Bj Services Company Method of treating an oil or gas well with biodegradable low toxicity fluid system
US20070039896A1 (en) * 2005-05-23 2007-02-22 Bowden Robert W Oil cleaning system and method
US7588682B2 (en) * 2005-10-04 2009-09-15 Kevin Norman Process and apparatus for enhanced recovery of oil from oily particulate material
US20100043902A1 (en) * 2005-10-04 2010-02-25 Kevin Norman Process and Apparatus for Enhanced Recovery of Oil From Oily Particulate Material
US20070287636A1 (en) * 2006-06-09 2007-12-13 Sun Drilling Products Corporation Drilling fluid additive and base fluid compositions of matter containing B100 biodiesels; and applications of such compositions of matter in well drilling, completion, and workover operations
US20070299271A1 (en) * 2006-06-27 2007-12-27 Udaya Nayanskantha Wanasundara Process for separating saturated and unsaturated fatty acids for producing cold-tolorant biodiesel fuel from soy oil
US20090090658A1 (en) * 2007-10-04 2009-04-09 Zvonko Burkus Methods for enhancing efficiency of bitumen extraction from oil sands using lipids and lipid by-products as process additives
MX2008014694A (en) * 2008-11-19 2009-11-19 Green Zone S A De C V Process for the reduction of viscosity in heavy hydrocarbons.
US9708521B2 (en) 2010-03-08 2017-07-18 Georgetown University Systems and methods employing low molecular weight gelators for crude oil, petroleum product or chemical spill containment and remediation
US9109150B2 (en) 2010-03-08 2015-08-18 Georgetown University Fast recovery of thixotropy by organogels with low molecular weight gelators
MX337888B (en) 2010-06-28 2016-03-09 Geo Estratos S A De C V Asphaltene-controlling additive compound for oil.
CA2809411A1 (en) * 2010-08-26 2012-04-12 Georgetown University Low molecular weight gelators for crude oil, petroleum product or chemical spill containment
US8955589B2 (en) 2010-12-20 2015-02-17 Intevep, S.A. Formulation and method of use for stimulation of heavy and extraheavy oil wells
US20120157357A1 (en) * 2010-12-20 2012-06-21 Intevep, S.A. Detergent package for improved recovery and transport of crude oil
US8871021B2 (en) * 2011-03-08 2014-10-28 Staker & Parson Companies Concrete mixtures including carbon encapsulating admixture
US20120279714A1 (en) * 2011-05-04 2012-11-08 Timothy Lesko Chemical line flush systems
RU2559976C2 (en) * 2013-07-10 2015-08-20 Мидхат Кавсарович Исаев Chemical for oil deposit development and method of oil deposit development using this chemical
US10081760B2 (en) 2014-01-16 2018-09-25 Elevance Renewable Sciences, Inc. Olefinic ester compositions and their use in stimulating hydrocarbon production from a subterranean formation
WO2015108872A1 (en) * 2014-01-16 2015-07-23 Elevance Renewable Sciences, Inc. Olefinic ester compositions and their use as cleaning agents
US11053430B2 (en) 2014-01-16 2021-07-06 Wilmar Trading Pte Ltd. Olefinic ester compositions and their use in stimulating hydrocarbon production from a subterranean formation
US10759990B2 (en) 2014-01-16 2020-09-01 Wilmar Trading Pte Ltd. Use of olefinic ester compositions in oil and gas fields
MX2014006332A (en) * 2014-05-26 2015-11-26 Itzeder Alejandro Isunza Rebolledo Oil-based compositions for dispersing asphaltenes and paraffins.
WO2016004401A1 (en) 2014-07-03 2016-01-07 Solazyme, Inc. Lubricants and wellbore fluids
US10041314B2 (en) * 2014-07-08 2018-08-07 National Oilwell Varco, L.P. Closed loop drilling mud cooling system for land-based drilling operations
KR20160045467A (en) 2014-10-17 2016-04-27 에스케이이노베이션 주식회사 Method of making drilling fluid from fat and oil in biomass
US9914867B2 (en) * 2016-02-16 2018-03-13 Noles Intellectual Properties, Llc Completion fluid friction reducer
WO2019028086A1 (en) * 2017-07-31 2019-02-07 Chevron U.S.A. Inc. Injection fluids for stimulating fractured formations
CN110894783B (en) * 2018-09-13 2022-03-01 中国石油天然气股份有限公司 Method for calculating validity period of oil-gas well production increasing measures
US20230183550A1 (en) * 2019-05-01 2023-06-15 Richard Strother Bio-derived complex for oil and gas well remediation
US20230131064A1 (en) * 2020-03-20 2023-04-27 Metss Corp. Brine-tolerant lubricants and methods for using the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4964615A (en) * 1988-01-20 1990-10-23 Henkel Kommanditgesellschaft Auf Aktien Compositions for freeing jammed drill pipes
WO2000027945A1 (en) * 1998-11-12 2000-05-18 M-I L.L.C. Invert emulsion drilling fluids having negative alkalinity
US6218342B1 (en) * 1996-08-02 2001-04-17 M-I Llc Oil-based drilling fluid

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2238671A (en) * 1940-02-09 1941-04-15 Du Pont Method of treating wells
US2721174A (en) 1952-09-06 1955-10-18 Stanolind Oil & Gas Co Emulsified acids for high temperature wells
US2927639A (en) 1956-11-23 1960-03-08 Swift & Co Surfactant treatment of oil and gas wells
US3163214A (en) 1961-11-13 1964-12-29 Pure Oil Co Solvent-waterflood oil recovery process
US3354033A (en) * 1964-06-01 1967-11-21 Buckman Labor Inc Compositions containing monosubstituted 2-bromoacetophenones and processes of utilizing the same
US3696040A (en) 1970-01-16 1972-10-03 Champion Chem Inc Composition for removal of calcium sulfate deposits
US3873452A (en) 1970-12-07 1975-03-25 Amoco Prod Co Acidizing oil wells
US3817330A (en) * 1972-03-29 1974-06-18 Texaco Inc Secondary recovery method
US4064942A (en) * 1976-07-21 1977-12-27 Shell Canada Limited Aquifer-plugging steam soak for layered reservoir
US4532052A (en) 1978-09-28 1985-07-30 Halliburton Company Polymeric well treating method
US4252192A (en) 1979-07-02 1981-02-24 Stepan Chemical Company Process for enhanced oil recovery employing petroleum sulfonates
US4371444A (en) 1980-01-16 1983-02-01 Texaco Inc. Process for secondary recovery
US4556107A (en) 1983-04-28 1985-12-03 Chevron Research Company Steam injection including alpha-olephin sulfonate dimer surfactant additives and a process of stimulating hydrocarbon recovery from a subterranean formation
US4556495A (en) 1983-06-28 1985-12-03 Phillips Petroleum Company Immiscible displacement of oil with surfactant system
US4793414A (en) 1986-11-26 1988-12-27 Chevron Research Company Steam injection profiling
US4958684A (en) 1986-11-26 1990-09-25 Chevron Research Company Steam injection profiling
DE3644386A1 (en) 1986-12-24 1988-07-07 Huels Chemische Werke Ag METHOD FOR OBTAINING PETROLEUM FROM AN UNDERGROUND DEPOSIT BY SURFACTANT FLOODS
US4817713A (en) 1987-08-19 1989-04-04 Chevron Research Company Steam injection profiling
US5244878A (en) 1987-12-30 1993-09-14 Institut Francais Du Petrole Process for delaying the formation and/or reducing the agglomeration tendency of hydrates
US4966235A (en) 1988-07-14 1990-10-30 Canadian Occidental Petroleum Ltd. In situ application of high temperature resistant surfactants to produce water continuous emulsions for improved crude recovery
US4967837A (en) 1989-03-31 1990-11-06 Chevron Research Company Steam enhanced oil recovery method using dialkyl aromatic sulfonates
US5110487A (en) 1989-04-03 1992-05-05 Chevron Corporation Enhanced oil recovery method using surfactant compositions for improved oil mobility
US4934457A (en) 1989-07-18 1990-06-19 Wallender Kenneth D Composition and method for stimulating wells
US5131471A (en) 1989-08-16 1992-07-21 Chevron Research And Technology Company Single well injection and production system
US5014787A (en) 1989-08-16 1991-05-14 Chevron Research Company Single well injection and production system
US5273682A (en) 1989-09-22 1993-12-28 Chevron Research And Technology Company Viscosity control additives for foaming mixtures
US5052487A (en) 1989-12-29 1991-10-01 Chevron Research & Technology Company Sequential injection foam process for enhanced oil recovery
US5188178A (en) 1991-08-01 1993-02-23 Texaco Inc. Method and apparatus for automatic well stimulation
US5193618A (en) 1991-09-12 1993-03-16 Chevron Research And Technology Company Multivalent ion tolerant steam-foaming surfactant composition for use in enhanced oil recovery operations
US5234054A (en) 1991-09-12 1993-08-10 Chevron Research And Technology Company Method for foam emplacement in gas flooding for enhanced oil recovery
US5201815A (en) 1991-12-20 1993-04-13 Chevron Research And Technology Company Enhanced oil recovery method using an inverted nine-spot pattern
US5773390A (en) 1994-07-01 1998-06-30 Well-Flow Technologies, Inc. Chemical additive for removing solids from a well drilling system
FR2727126B1 (en) * 1994-11-22 1997-04-30 Inst Francais Du Petrole LUBRICATING COMPOSITION COMPRISING AN ESTER. USE OF THE COMPOSITION AND WELL FLUID COMPRISING THE COMPOSITION
US5547022A (en) 1995-05-03 1996-08-20 Chevron U.S.A. Inc. Heavy oil well stimulation composition and process
US5797456A (en) 1995-08-08 1998-08-25 Nalco/Exxon Energy Chemicals,L.P. Surfactant additive for oil field acidizing
CO4560488A1 (en) * 1995-10-03 1998-02-10 Nor Ind Inc CLEANING COMPOSITIONS FOR LINE WELLS, HOUSINGS, TRAININGS AND OIL AND GAS EQUIPMENT.
US5905061A (en) * 1996-08-02 1999-05-18 Patel; Avind D. Invert emulsion fluids suitable for drilling
US6589917B2 (en) * 1996-08-02 2003-07-08 M-I Llc Invert emulsion drilling fluids and muds having negative alkalinity and elastomer compatibility
US6096699A (en) * 1999-09-03 2000-08-01 Ntec Versol, Llc Environmentally friendly solvent
US6593279B2 (en) * 1999-12-10 2003-07-15 Integrity Industries, Inc. Acid based micro-emulsions
US6766817B2 (en) 2001-07-25 2004-07-27 Tubarc Technologies, Llc Fluid conduction utilizing a reversible unsaturated siphon with tubarc porosity action
US6784147B1 (en) * 2003-07-03 2004-08-31 State Industrial Products Soy based drain cleaner

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4964615A (en) * 1988-01-20 1990-10-23 Henkel Kommanditgesellschaft Auf Aktien Compositions for freeing jammed drill pipes
US6218342B1 (en) * 1996-08-02 2001-04-17 M-I Llc Oil-based drilling fluid
WO2000027945A1 (en) * 1998-11-12 2000-05-18 M-I L.L.C. Invert emulsion drilling fluids having negative alkalinity

Cited By (11)

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AU2002359795A1 (en) 2003-07-15
US6776234B2 (en) 2004-08-17
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