Patent Application
20250163312
Asphaltenes are a major component in crude oil, and there is general agreement as to the deleterious effects of asphaltenes in the reduction of oil extraction and processing in the petrochemical industry. Asphaltenes can deposit in the pores of formations, blocking the flow of fluids. Additionally, asphaltenes can precipitate from a stream of oil and coat boreholes, production tubing, sand screens, and transport lines. Moreover, in a processing facility, asphaltenes can foul processing equipment and poison catalysts. Accordingly, methods for removing asphaltene deposits from oil environments such as a reservoir would be well received in the art.
A method of removing deposits from a substrate includes contacting the deposits with a treatment fluid comprising a solvent and an additive composition comprising at least one of an alkylbenzene sulfonic acid or an alkylbenzene sulfonate; and separating the deposits from the substrate with the treatment fluid to remove the deposits from the substrate, wherein the deposits comprise asphaltenes.
The following descriptions should not be considered limiting in any way. With reference to the accompanying drawings, like elements are numbered alike:
Asphaltenes are components of crude oils and can contain numerous individual compounds, particularly high molecular weight condensed aromatic compounds including heteroatoms such as sulfur, oxygen, nitrogen, and the like. The heteroatoms may be part of the aromatic ring system or part of other carbocyclic rings, linking groups, substituents, or functional groups. Aromatic solvents can be used to remove asphaltene deposits. However, due to the complexity of the asphaltene chemistry, a solvent which is effective to remove certain asphaltene molecules may not be effective to remove asphaltenes having more complex structures. In such circumstances, when applying solvents to remove asphaltene deposition in a formation, a pressure increase in regard to surface treating pressure may be observed. This can be considered an unfavorable response by operators who would prefer to see a pressure decline.
The inventors have discovered a treatment fluid that can effectively remove asphaltene deposits with improved injection pressure during pumping treatments. In addition to improved performance over an asphaltene solvent, another advantage is the time that is saved when applying the treatment fluid. Often when injection pressure increases are encountered, solvents are pumped at lower rates which can result in extra time to complete a treatment. The treatment fluid as described removes asphaltenes without pressure increase, thus providing a fast and efficient asphaltene removal method. The method can also improve injectivity and wetting characteristics, and stimulate production in wells damaged or impaired by asphaltene deposition.
The treatment fluid comprises a solvent and an additive composition. The solvent can comprise an aromatic solvent, optionally in combination with a co-solvent. The aromatic solvent can be, for example, toluene, xylenes, or light aromatic naphtha, or a combination comprising at least one of the foregoing aromatic solvent. As used herein, a light aromatic naphtha refers to a combination of hydrocarbons obtained from distillation of aromatic streams. The light aromatic naphtha can consist predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135° C. to 210° C. (275° F. to 410° F.). The light aromatic naphtha can have a CAS #64742-95-6. A content of the aromatic solvent can be about 10 to about 99 or about 90 volume percent, preferably about 15 to about 75 volume percent, more preferably about 30 to about 60 volume percent, based on a total volume of the treatment fluid.
The co-solvent can include at least one of an alcohol, an amine, an amide, an ether, an ester, a ketone, acetonitrile, dimethylsulfoxide, or a carbonate such as propylene carbonate.
The alcohol can be a mono or polyhydric alcohol having 1 to 8 carbon atoms. The alcohol can also include one or more ether moiety. Examples of the alcohol include methanol, ethanol, n-propanol, iso-propanol, butanol, glycerol, a glycol such as ethylene glycol; propylene glycol; and diethylene glycol, 2-methyl-hexanol, 1-methoxy-2-propanol, and 2-butoxyethanol.
Examples of the amine include methylamine, diethyl amine, and tributyl amine. Examples of the amide include dimethylformamide. The ether can include diethyl ether, polyether, and tetrahydrofuran. The ester can include ethyl acetate, methyl butyrate, and the like. An example of the ketone is acetone.
If present, a content of the co-solvent can be about 0 or greater than 0 to about 90 volume percent, preferably about 0.1 to about 40 volume percent, about 0.1 volume percent to about 30 volume percent, more preferably about 0.5 volume percent to about 15 volume percent, based on a total volume of the treatment fluid. In an aspect, the solvent comprises both the aromatic solvent and the co-solvent, and a volume ratio of the aromatic solvent relative to the co-solvent is about 100:0 to about 10:90, preferably about 99.9:0.1 to about 85:15.
The additive composition comprises an alkylbenzene sulfonic acid or an alkylbenzene sulfonate. Without wishing to be bound by theory, it is believed that the solvent can react with the asphaltene, facilitating the removal of asphaltene deposits from the substrate, and the additive composition, for example, the alkylbenzene sulfonate can keep the asphaltene small and dispersed, instead of precipitating. The alkylbenzene sulfonic acid can be a linear alkylbenzene sulfonic acid (LAS) or a branched alkylbenzene sulfonic acid (BAS). Preferably, the alkylbenzene sulfonic acid is a C5-25, C8-20, C10-20, or C10-18 alkyl benzene sulfonic acid such as dodecylbenzenesulfonic acid and 2-hexadecylbenzene sulfonic acid. An alkylbenzene sulfonate can include a salt of an alkylbenzene sulfonic acid. Suitable salts can be a sodium salt, a magnesium salt, an ammonium salt, or an amine salt. A content of the alkylbenzene sulfonic acid, the alkylbenzene sulfonate, or a combination thereof can be about 0.1 to about 99 volume percent, preferably about 0.5 to about 90 volume percent, more preferably about 1 to about 75 volume percent, based on a total volume of the additive composition.
The additive composition can also comprise an additional surfactant other than an alkylbenzene sulfonic acid or an alkylbenzene sulfonate. In an aspect, the additional surfactant comprises sodium trideceth sulfate. The additional surfactant can be present in an amount of about 0 or about 0.1 to about 20 volume percent, preferably about 0 or about 0.1 to about 15 volume percent, and more preferably about 0 or about 0.5 to about 12 volume percent, based on the total volume of the additive composition.
The additive composition can further include an acid component. Using an acid component can be particularly beneficial when the deposits also include inorganic scales mixed with asphaltenes. The acid component can include an acid, an acid precursor, or a combination thereof. The acid can be an inorganic acid such as HCl; H2SO4; HF; and HNO3, an organic acid such as acetic acid; glacial acetic acid; formic acid; lactic acid; citric acid; phthalic acid; or an amino acid such as glutamic acid. Acid precursors can include esters or anhydrides such as acetic anhydride. Combinations of the acids and/or acid precursors can be used.
The acid component can be present in an amount of about 0 or about 0.1 to about 80 volume percent, about 0 or about 0.1 to about 50 volume percent, preferably about 0 or about 0.5 to about 30 volume percent, based on a total volume of the additive composition.
The treatment fluid can be prepared by combing the solvent and the additive composition. A content of the additive composition can be about 0.1 to about 99 volume percent, preferably about 0.5 to about 70 volume percent, more preferably, about 1 to about 50 volume percent, based on a total volume of the treatment fluid. Preferably, the treatment fluid is a homogeneous single phase fluid.
As a specific example, the treatment fluid can comprise or consist of about 10 to about 99 volume percent, preferably about 15 to about 75 volume percent, more preferably about 30 to about 60 volume percent of an aromatic solvent comprising at least one of toluene, xylenes, or a low aromatic naphtha, and about 0 to about 50 volume percent, about 0.1 to about 40 volume percent, or about 0.5 to about 15 volume percent of a co-solvent comprising at least one of an alcohol, an amine, an amide, an ether, an ester, a ketone, acetonitrile, dimethylsulfoxide, or a carbonate, each based on a total volume of the treatment fluid; and about 0.5 to about 70 volume percent, preferably about 1 to about 40 volume percent of the additive composition, wherein the additive composition comprises about 0.5 to about 99 or about 70 volume percent, preferably about 1 to about 50 volume percent of a C5-25 alkylbenzene sulfonic acid or a salt thereof, and about 0 or about 0.1 to about 12 or about 10 volume percent, preferable about 0 or about 0.5 to about 5 volume percent of an additional surfactant comprising sodium trideceth sulfate, and about 0 or about 0.1 to about 50 volume percent, preferably about 0 or about 0.5 to about 30 volume percent, or about 0.5 to about 8 volume percent of an acid component, each based on a total volume of the additive composition.
The treatment fluid is effective to remove deposits from a substrate. The deposits can include organic deposits and optionally inorganic scales. The organic deposits include asphaltenes, and optionally resins and/or paraffin wax, and the like. The substrate can be formation, downhole element such as tubular; proppants; production tubing; sand screens; transport lines; or other downhole equipment including the surfaces thereof, a metal, composite, sand, rock, mineral, glass, or a combination comprising at least one of the foregoing.
The deposits, which are disposed on the substrate, can be removed from the substrate by contacting the deposits with the treatment fluid. Beneficially, the methods described herein, e.g., contacting the deposits with the treatment fluid, can be performed in an environment such as a pipeline, downhole, formation, tubular, frac feature (e.g., a vein or pore), production zone, reservoir, refinery, transport tube, production tube, or a combination thereof.
In an aspect, contacting the deposits with the treatment fluid is performed in a subsurface environment including but is not limited to a near-wellbore region. In such a instance, the method can include introducing the treatment fluid into the subsurface environment. Any known methods can be used. The treatment fluid can be introduced into a subsurface environment through an umbilical line, a coil tubing, or via a bullhead method through a flowline or a tubing. For example, a squeeze operation can be used to deliver the treatment fluid to a reservoir or a near-wellbore region. In another embodiment for the production of petroleum, the treatment fluid can be applied in a continuous or batch injection process through a capillary line, down the backside of well annuluses, through an umbilical line, or through an umbilical/capillary line combination.
Advantageously, the process does not restrict injection pressure. As shown in in
The treatment fluid can contact the deposits at a temperature of about 30° F. to about 450° F., preferably about 100° F. to about 400° F. Moreover, the deposits can be removed from the environment after separating the deposits from the substrate.
The treatment fluid can be used to remove deposits during a fracturing, acidizing, sand control, remedial, completion, or refracturing operation. In an embodiment, the deposits are removed during a pumping treatment placed in a completion or remedial operation. Such a treatment allows connectivity with establishing flow from reservoir to wellbore.
The treatment fluid can also be used as a solvent pre flush. In other words, the treatment fluid can be injected into a subsurface environment to contact the deposits, then a solvent as described herein (without the additive composition) can be injected into the subsurface environment to remove the deposits from the substrate for enhanced contact during acid treatments or other operations.
The method as described herein can enhance oil recovery in a reservoir, borehole, downhole, production zone, formation, or a combination thereof. For example, removal of the deposits that constrict flow can restore flow in a plugged reservoir. Additionally, the method can increase permeability in porous media (e.g., a sand screen) and flow channels (e.g., a crack in a formation filled with proppant obtained in a fracking process). Removal of asphaltenes from pores of a rock formation, within a reservoir, or from a sidewall of a tubular, production tubing, borehole, or transportation tube can improve the permeability of such structures, leading to increased quality of oil as well as enhanced oil recovery.
The treatment fluid can decrease the viscosity of crude oil making the oil more mobile for better recovery. This is especially important for heavy crude recovery.
Set forth below are various aspects of the disclosure.
Aspect 1. A method of removing deposits from a substrate, the method comprising: contacting the deposits with a treatment fluid comprising a solvent and an additive composition comprising at least one of an alkylbenzene sulfonic acid or an alkylbenzene sulfonate; and separating the deposits from the substrate with the treatment fluid to remove the deposits from the substrate, wherein the deposits comprise asphaltenes.
Aspect 2. The method as in any prior aspect, wherein the solvent comprises an aromatic solvent; and the aromatic solvent comprises at least one of toluene, xylenes, or a light aromatic naphtha; and a content of the aromatic solvent is about 10 volume percent to about 99 volume percent, based on a total volume of the treatment fluid.
Aspect 3. The method as in any prior aspect, wherein the solvent further comprises a co-solvent comprising at least one of an alcohol, an amine, an amide, an ether, an ester, a ketone, acetonitrile, dimethylsulfoxide, or a carbonate, and a content of the co-solvent is about 0.1 to about 50 volume percent, based on a total volume of the treatment fluid.
Aspect 4. The method as in any prior aspect, wherein a content of the additive composition is about 0.5 to about 75 or 70 volume percent, based on a total volume of the treatment fluid.
Aspect 5. The method as in any prior aspect, wherein the additive composition comprises the alkylbenzene sulfonic acid, and a content of the alkylbenzene sulfonic acid is about 0.5 to about 99 or 90 volume percent, based on a total volume of the additive composition.
Aspect 6. The method as in any prior aspect, wherein the additive composition comprises the alkylbenzene sulfonate, a content of the alkylbenzene sulfonate is about 0.5 to about 99 volume percent, based on a total volume of the additive composition.
Aspect 7. The method as in any prior aspect, wherein the alkylbenzene sulfonate is a salt of an alkylbenzene sulfonic acid.
Aspect 8. The method as in any prior aspect, wherein the additive composition further comprises an additional surfactant comprising sodium trideceth sulfate.
Aspect 9. The method as in any prior aspect, wherein the additive composition further comprises an acid component.
Aspect 10. The method as in any prior aspect, wherein the treatment fluid comprises about 10 to about 99 volume percent of an aromatic solvent, which comprises at least one of toluene, xylenes, or a low aromatic naphtha, and about 0 to about 50 volume percent of a co-solvent comprising at least one of an alcohol, an amine, an amide, an ether, an ester, a ketone, acetonitrile, dimethylsulfoxide, or a carbonate, each based on a total volume of the treatment fluid; and about 0.5 to about 70 volume percent of the additive composition, the additive composition comprising about 0.5 to about 99 or 70 volume percent of a C8-30 alkylbenzene sulfonic acid or a salt thereof; and about 0 to about 12 volume percent of an additional surfactant comprising sodium trideceth sulfate, and about 0 to about 50 volume percent of an acid component, each based a total volume of the additive composition.
Aspect 11. The method as in any prior aspect, wherein the treatment fluid is a homogeneous single phase fluid.
Aspect 12. The method as in any prior aspect, wherein the deposits further comprise at least one of a resin, a paraffin wax, or an inorganic scale.
Aspect 13. The method as in any prior aspect, wherein contacting the deposits with the treatment fluid is performed in an environment comprising at least one of a pipeline, a formation, a production zone, a reservoir, or a downhole element.
Aspect 14. The method as in any prior aspect, wherein the deposits are removed from the substrate during a fracturing, acidizing, sand control, remedial, completion, or refracturing operation.
Aspect 15. The method as in any prior aspect, wherein the deposits are removed during a pumping treatment placed in a completion or remedial operation. The method can establish flow from a reservoir to a wellbore.
Aspect 16. The method as in any prior aspect, further comprising introducing the treatment fluid into a subsurface environment through an umbilical line, a coil tubing, or via a bullhead method through a flowline or a tubing.
Aspect 17. The method as in any prior aspect, wherein contacting the deposits with the treatment fluid is performed in a near-wellbore region, and the method comprises cleaning the near-wellbore region and a downhole element in the near-wellbore region with the treatment fluid.
Aspect 18. The method as in any prior aspect, wherein the method comprises injecting into a subsurface environment the treatment fluid as a pre-flush fluid such that the treatment fluid contacts the deposits on the substrate, and injecting into the subsurface environment an aromatic solvent without the alkylbenzene sulfonic acid or the alkylbenzene sulfonate.
Aspect 19. The method as in any prior aspect, wherein the substrate comprises at least one of a formation, a downhole element, a metal, a composite, sand, rock, a mineral, or glass.
Aspect 20. The method as in any prior aspect, further comprising enhancing oil recovery from a subsurface environment.
Aspect 21. The method as in any prior aspect, further comprising reducing the viscosity of oil in the subsurface environment.
All ranges disclosed herein are inclusive of the endpoints, and the endpoints are independently combinable with each other. As used herein, “combination” is inclusive of blends, mixtures, alloys, reaction products, and the like. All references are incorporated herein by reference.
The use of the terms “a” and “an” and “the” and similar referents in the context of describing the invention (especially in the context of the following claims) are to be construed to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The modifier “about” used in connection with a quantity is inclusive of the stated value and has the meaning dictated by the context (e.g., it includes the degree of error associated with measurement of the particular quantity). In an embodiment, the term “about” means that the value associated with about can vary by 10%. As used herein, size means largest dimension. Unless defined otherwise, technical and scientific terms used herein have the same meaning as is commonly understood by one of skill in the art to which this invention belongs.
All references cited herein are incorporated by reference in their entirety. While typical embodiments have been set forth for the purpose of illustration, the foregoing descriptions should not be deemed to be a limitation on the scope herein. Accordingly, various modifications, adaptations, and alternatives can occur to one skilled in the art without departing from the spirit and scope herein.
