Patent Application
20150218921
Embodiments of the disclosure relate generally to methods and systems of forming a stabilized emulsion and extracting a hydrocarbon material from a subterranean formation.
Water flooding is a conventional process of enhancing the extraction of hydrocarbon materials (e.g., crude oil, natural gas, etc.) from subterranean formations. In this process, an aqueous fluid (e.g., water, brine, etc.) is injected into the subterranean formation through injection wells to sweep a hydrocarbon material contained within interstitial spaces (e.g., pores, cracks, fractures, channels, etc.) of the subterranean formation toward production wells offset from the injection wells. One or more additives may be added to the aqueous fluid to assist in the extraction and subsequent processing of the hydrocarbon material.
For example, in some approaches, a surfactant, solid particles (e.g., colloids), or both are added to the aqueous fluid. The surfactant and/or the solid particles can adhere to or gather at interfaces between a hydrocarbon material and an aqueous material to form a stabilized emulsion of one of the hydrocarbon material and the aqueous material dispersed in the other of the hydrocarbon material and the aqueous material. Surfactants may decrease the surface tension between the hydrocarbon phase and the water phase, such as, for example, in an emulsion of a hydrocarbon phase dispersed within an aqueous phase. Stabilization by the surfactant, the solid particles, or both, lowers the interfacial tension between the hydrocarbon and water and reduces the energy of the system, preventing the dispersed material (e.g., the hydrocarbon material, or the aqueous material) from coalescing, and maintaining the one material dispersed as units (e.g., droplets) throughout the other material. Reducing the surface tension increases the permeability and the flowability of the hydrocarbon material. As a consequence, the hydrocarbon material may be more easily transported through and extracted from the subterranean formation as compared to water flooding processes that do not employ the addition of a surfactant and/or solid particles. The effectiveness of the emulsion is determined in large part by the ability of the emulsion to remain stable and ensure mixing of the two phases.
However, application of surfactants is usually limited by the cost of the chemicals and their adsorption and loss onto the rock of the hydrocarbon-containing formation. Disadvantageously, the affectivity of various surfactants can be detrimentally reduced in the presence of dissolved salts (e.g., such as various salts typically present within a subterranean formation). In addition, surfactants can have a tendency to adhere to surfaces of the subterranean formation, requiring the economically undesirable addition of more surfactant to the injected aqueous fluid to account for such losses. Solid particles can be difficult to remove from the stabilized emulsion during subsequent processing, preventing the hydrocarbon material and the aqueous material thereof from coalescing into distinct, immiscible components, and greatly inhibiting the separate collection of the hydrocarbon material. Furthermore, the surfactants are often functional or stable only within particular temperature ranges and may lose functionality at elevated temperatures or various conditions encountered within a subterranean formation.
Embodiments disclosed herein include methods of recovering hydrocarbon material from a subterranean formation or from a bituminous sand, as well as related stabilized emulsions. For example, in accordance with one embodiment, a method of recovering a hydrocarbon material comprises combining amphiphilic nanoparticles comprising a carbon core, at least one hydrophilic group, and at least one hydrophobic group with a carrier fluid to form a suspension, contacting at least one of a subterranean formation and a slurry comprising bituminous sand and water with the suspension to form an emulsion stabilized by the amphiphilic nanoparticles, and removing hydrocarbons from the emulsion stabilized by the amphiphilic nanoparticles.
In additional embodiments, a method of removing a hydrocarbon from a subterranean formation comprises forming at least one hydrophilic group on a surface of a carbon-containing material comprising at least one of a carbon nanotube, a fullerene, a carbon nanodiamond, graphene, and graphene oxide, mixing the carbon-containing material with a carrier fluid to form a suspension, introducing the suspension into a subterranean formation and contacting hydrocarbons within the subterranean formation with the carrier fluid suspension to form an emulsion stabilized by the carbon-containing material, and transporting the emulsion to a surface of the subterranean formation.
In further embodiments, a suspension for removing hydrocarbons from a subterranean formation comprises a plurality of carbon-containing amphiphilic nanoparticles, the amphiphilic nanoparticles comprising hydrophobic functional groups on a surface of the carbon-containing material, and hydrophilic functional groups on another surface of the carbon-containing material. The suspension further comprises a carrier fluid carrier fluid.
While the specification concludes with claims particularly pointing out and distinctly claiming what are regarded as embodiments of the invention, the advantages of embodiments of the disclosure may be more readily ascertained from the following description of certain embodiments of the disclosure when read in conjunction with the accompanying drawings, in which:
Illustrations presented herein are not meant to be actual views of any particular material, component, or system, but are merely idealized representations that are employed to describe embodiments of the disclosure.
The following description provides specific details, such as material types, compositions, and processing conditions in order to provide a thorough description of embodiments of the disclosure. However, a person of ordinary skill in the art will understand that the embodiments of the disclosure may be practiced without employing these specific details. Indeed, the embodiments of the disclosure may be practiced in conjunction with conventional techniques employed in the industry. Only those process acts and structures necessary to understand the embodiments of the disclosure are described in detail below. Additional acts or materials to extract a hydrocarbon material from a subterranean formation or from bituminous sands (e.g., oil sands, tar sands, etc.) may be performed by conventional techniques.
Methods of forming amphiphilic nanoparticles with dual functionality are described. As used herein, the term “nanoparticle” means and includes a particle having an average particle width or diameter of less than about 1,000 nm. As used herein, “amphiphilic nanoparticle” means and includes a nanoparticle exhibiting both hydrophilic and hydrophobic properties (e.g., similar to a Janus nanoparticle). The amphiphilic nanoparticle may include a two-dimensional structure with one side of the structure exhibiting hydrophobic characteristics and another, opposite side of the structure exhibiting hydrophilic characteristics. For example, an amphiphilic nanoparticle may include both hydrophilic and hydrophobic functional groups. In other embodiments, the amphiphilic nanoparticle may be formed of a hydrophobic core material and at least one side or portion of the hydrophobic core material may be functionalized with hydrophilic functional groups. Surfactants including such amphiphilic nanoparticles may have a higher surface area and may be stable at higher temperatures and salt concentrations than conventional particle surfactants used to stabilize emulsions. In addition, functional groups on the amphiphilic nanoparticles may be formulated to interact with various media of different subterranean environments.
The amphiphilic nanoparticles may gather at, adhere to, and/or adsorb onto minerals within a subterranean formation, may adsorb to interfaces of a hydrocarbon material and an aqueous material, or both. The amphiphilic nanoparticles may form a stabilized emulsion (e.g., a Pickering emulsion) comprising units of one of the hydrocarbon material and the aqueous material. As used herein, the term “emulsion” refers to suspensions of droplets of one immiscible fluid dispersed in another fluid. The emulsion may reduce the interfacial tension between a continuous phase and a dispersed phase. Decreasing interfacial tension between, for example, a dispersed hydrocarbon phase and a continuous aqueous phase may increase the hydrocarbon (e.g., oil) mobility and recovery from a subterranean formation or from a slurry of a bituminous sand including the hydrocarbon.
The amphiphilic nanoparticles may be formulated to remain at an interface between a polar phase and a nonpolar phase, between a hydrophilic phase and a hydrophobic phase, and/or between a hydrocarbon phase and an aqueous phase, such as at an interface between a gas phase and an aqueous phase, an interface between a liquid hydrocarbon phase and an aqueous phase, or an interface between a solid phase and at least one of an aqueous phase and a hydrocarbon phase. The amphiphilic nanoparticles may stabilize an emulsion of the hydrocarbon phase within the aqueous phase or an emulsion of the aqueous phase within the hydrocarbon phase. Stabilizing the emulsion may prevent the emulsion from coalescing once the emulsion interface is formed. One side (e.g., the hydrophilic side) of the amphiphilic nanoparticles may be formulated to be attracted to the aqueous phase while the other side (e.g., the hydrophobic side) of the amphiphilic nanoparticles may be formulated to be attracted to the hydrocarbon phase.
The amphiphilic nanoparticles formed by the methods described herein may have a higher surface area than conventional surfactants. The functionalized surfaces of the amphiphilic nanoparticles may be formulated to interact with the interface between the hydrocarbon phase and the aqueous phase or with solid surfaces (e.g., minerals) within the subterranean formation, thereby forming a stable emulsion of a continuous aqueous or hydrocarbon phase and a dispersed phase of the other of the hydrocarbon and aqueous phase. The stability of the emulsion may be controlled by one or more of controlling the solubility of the amphiphilic nanoparticles within the aqueous phase, controlling the pH of the emulsion and/or the aqueous phase, and controlling the surface charge of the amphiphilic nanoparticles.
Referring to
The base portion may include any material that may be chemically modified with functional groups to form the hydrophilic portion 102 and the hydrophobic portion 104. In some embodiments, the base portion includes a silica base. In other embodiments, the base portion includes a metal or a metal oxide. For example, the base portion may include a metal such as iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, cobalt, oxides thereof and combinations thereof. In yet other embodiments, the base portion may include a carbon-based material, such as at least one of carbon nanotubes (e.g., single-walled carbon nanotubes (SWCNTs), multi-walled carbon nanotubes (MWCNTs), and combinations thereof), carbon nanodiamonds, graphite, graphene, graphene oxide, fullerenes, onion-like structures (e.g., a “bucky onion”). Thus, the base portion may include silica, a metal such as one of iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, cobalt, carbon nanotubes, carbon nanodiamonds, graphene, graphene oxide, fullerenes, bucky onions, and combinations thereof.
The amphiphilic nanoparticle 100 may be formed from a plurality of hydrophilic precursors and a plurality of hydrophobic precursors. As used herein, the term “hydrophilic precursor” includes materials having at least one atom of carbon, silicon, iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt, and at least one hydrophilic functional group. As used herein, the term “hydrophobic precursor” includes materials having at least one atom of carbon, silicon, iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt, and at least one hydrophobic functional group. In some embodiments, a plurality of hydrophilic precursors may react to form a nanoparticle including a base of at least one of carbon, silica, a metal, and a metal oxide with one or more hydrophilic functional groups attached to the surface thereof. The hydrophilic functional groups of the hydrophilic portion 102 may be formed from the hydrophilic functional group of the hydrophilic precursor.
The surface of the base portion may be chemically modified to form amphiphilic nanoparticles 100 including a hydrophobic portion 104 in addition to the hydrophilic portion 102. The hydrophobic portion 104 may be formed from hydrophobic groups attached to the surface of the base portion. The hydrophobic groups may include nonpolar groups, such as, for example, alkyl chains. Where the base portion is formed of carbon (e.g., carbon nanotubes, carbon nanodiamonds, graphite, graphene, graphene oxide, fullerenes, bucky onions, etc.) the hydrophobic portion 104 may be comprised of the base portion and the hydrophilic portion 102 may be formed on at least some surfaces of the hydrophobic base portion. The hydrophilic portion 102 may be soluble in an aqueous phase, whereas the hydrophobic portion 104 may be soluble in an organic phase.
The amphiphilic nanoparticle 100 may be formed of various shapes. The shape of the amphiphilic nanoparticle 100 may be controlled by growing the amphiphilic nanoparticles 100 in the presence of a structure-directing agent. Non-limiting examples of structure-directing agents include polymers such as a polypyrrole (e.g., polyvinylpyrrolidone (PVP)), an oxidized polypyrrole, a diphenyl ester, and cetyltrimethylammonium bromide (CTAB). With continued reference to
In some embodiments, the hydrophilic portion 102 of the amphiphilic nanoparticles 100 is formed before forming the hydrophobic portion 104. In some embodiments, the hydrophilic portion 102 is formed by hydrolyzing the hydrophilic precursor. The hydrophilic precursor may include an organosilane having the general formula, RnSiX(4-n), where X is a hydrolyzable group, such as an alkoxy, acyloxy, amine, or halide group, and Rn includes a hydrophilic functional group. As used herein, the term “hydrolyzable group” means and includes a group that can be at least partially depolymerized to lower molecular weight units by hydrolysis (i.e., the cleavage of a chemical bond by the reaction with water). The hydrolyzable group may be reactive with an aqueous material, such as water.
The hydrophilic precursor may include one or more hydrophilic functional groups such as a hydroxyl group (—OH−), a carboxyl group (—COOH−), a carbonyl group (—C═O), an amino group (—NH3+, —NHR, —NRR′, where R and R′ include a hydrocarbon group, such as an alkyl group, an alkenyl group, an alkynyl group, an aryl group, each of which may include one or more hydrogen atoms substituted with one or more halides, hydroxyl groups, amine groups, or sulfur-containing groups), a thiol group (—SH), a phosphate group (—PO43−), or other hydrophilic or polar functional groups in addition to the hydrolyzable group.
In some embodiments, a carbon-containing material that forms the base portion may include one or more exposed functional groups such as a hydroxyl group, a carboxyl group, a carbonyl group, an amino group, a thiol group, a phosphate group, an azo group, or another hydrophilic or polar functional group. By way of example, carbon nanotubes may include one or more hydrophilic functional groups on at least one of the outside or the inside (e.g., an inner wall or an outer wall) of the carbon nanotube. In other embodiments, at least one side of graphite platelets, graphene platelets or graphene oxide platelets may be functionalized with at least one type of hydrophilic functional group.
By way of non-limiting example, a carbon-containing material may be functionalized by oxidation with concentrated nitric acid, sulfuric acid, and combinations thereof. The oxidation may form carboxyl groups on exposed surfaces of the carbon-containing material, such as on sidewalls of carbon nanotubes or on exposed surfaces of a graphene plate. The exposed carboxyl groups may form reaction sites for further functionalizing the carbon-containing material, in some embodiments, the exposed carboxyl groups may be exposed to an amine (primary amine (RNH2), a secondary amine (RR′NH), or a tertiary amine (RR′R″N), where R, R′, and R″ include a hydrocarbon group, such as an alkyl group, an alkenyl group, an alkynyl group, an aryl group, each of which may include one or more hydrogen atoms substituted with one or more halides, hydroxyl groups, amine groups, or sulfur-containing groups), an alkanolamine (a compound including a hydroxyl group and at least one of NH2, NHR, and NRR′ where R and R′ include the same groups described above with respect to amines) to form amine functionalized nanotubes. The amine groups attached to the carbon-containing base may form hydrophilic groups attached to the hydrophobic carbon-containing base.
In other embodiments, exposed hydroxyl groups of a carbon-containing core may react with other hydrophilic precursors including terminal hydroxyl groups in a condensation reaction to attach the hydrophilic portion 102 to the carbon-containing material. By way of example only, the terminal hydroxyl groups of a carbon-containing material may react with materials such as a hydroxylamine (e.g., HO—NRR′, where R and R′ include a hydrocarbon group as described above and include at least one hydrogen substituted with at least one of a halide, a hydroxyl group, an amine group, and a sulfur-containing compound) in a condensation reaction.
The hydrophilic precursor may include oxysilanes, orthosilicates, aminosilanes, silanols, epoxy silanes, metal oxides, hydroxides, metal hydroxides, or combinations thereof. As used herein, the term “oxysilane” means and includes materials including a silicon atom bonded to at least one oxygen atom (e.g., —Si—OR, where R is a hydrocarbon material or hydrogen). As used herein, the term “orthosilicate” means and includes materials including a silicon atom bonded to four oxygen atoms (e.g., Si(OR)4, where R is a hydrocarbon material or hydrogen).
The hydrophilic precursor may include orthosilicates, such as, for example, tetramethyl orthosilicate, tetraethyl orthosilicate (TEOS), tetrapropyl orthosilicate, trimethylmethoxysilane, triethylethoxysilane, or tripropylpropoxysilane. The hydrolysis of trimethylmethoxysilane, triethylethoxysilane, or tripropylpropoxysilane may form a silanol such as trimethylsilanol, triethylsilanol, or tripropyl silanol, respectively. In other embodiments, the hydrophilic precursor includes ethyoxysilanes such as trimethoxysilane, triethoxysilane, or tributykethoxy)silane.
In other embodiments, the hydrophilic precursor includes metal hydroxides and metal salts. For example, the hydrophilic precursor may include metal hydroxides such as an iron hydroxide, titanium hydroxide (e.g., TiO(OH)2, Ti(OH)4), germanium hydroxide, tin hydroxide, lead hydroxide, zirconium hydroxide, ruthenium hydroxide, nickel hydroxide, and cobalt hydroxide. In some embodiments, the hydrophilic precursor includes a metal salt such as salts of at least one of iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt. In some embodiments, a hydrophilic precursor including a metal hydroxide may react with an exposed hydroxyl group on a surface of the base of the nanoparticle.
In other embodiments, the hydrophilic precursor includes a metal oxide. For example, the hydrophilic precursor may include iron oxide (Fe2O3, Fe3O4), titanium dioxide, germanium oxide (GeO, GeO2), tin oxide (SnO, SnO2), lead oxide (PbO, PbO2, Pb3O4), zirconium oxide, ruthenium oxide (RuO2, RuO4), nickel oxide (NiO, Ni2O3), and cobalt oxide (CoO, Co2O3, Co3O4). In other embodiments, the hydrophilic precursor may include a metal alkoxide. For example, the hydrophilic precursor may include iron ethoxide, titanium isopropoxide, titanium ethoxide, germanium ethoxide, tin ethoxide, lead ethoxide, zirconium ethoxide, and nickel(II) methoxide.
In other embodiments, the hydrophilic precursor may include an aminosilane including at least one amino group. The at least one amino group may be in addition to at least two oxysilane groups. Non-limiting examples of suitable aminosilanes include (3-aminopropyl)-thethoxy-methylsilane (APDEMS), (3-aminopropyl)-trimethoxysilane (APTMS), (3-aminopropyl)-methyldiethoxysilane, (3-aminopropyl)-triethoxysilane (APTES), 3-aminopropyltriethoxysilane, bis(3-triethoxysilylpropyl) amine, and bis(3-trimethoxysilyiproply) amine. Hydrolysis of the aminooxysilanes may form a hydroxyl terminated hydrophilic portion 102 including amino groups. In some embodiments, the aminosilanes may be reacted with, for example, an ethylene carbonate to form a hydrophilic portion 102 including exposed hydroxyl groups.
In other embodiments, the hydrophilic precursor may include an epoxy silane. Non-limiting examples of epoxy silanes include 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, and 3-glycidyloxypropyltriethoxysilane. The epoxy silane may be hydrolyzed to form exposed hydroxyl groups on the hydrophilic portion 102.
The synthesis of the hydrophilic portion 102 of the amphiphilic nanoparticles 100 may be carried out in a polar solvent. The hydrophilic portion 102 may be soluble in the solvent. The solvent may include an alcohol such as methanol, ethanol, propanol, butanol, pentanol, other alcohol, acetone, or combinations thereof. The hydrophilic precursor may be soluble in the solvent.
Additional agents may be added to the reaction solution. For example, structure-directing agents, such as polyvinylpyrrolidone (PVP), may be mixed into the reaction solution. The pH of the reaction solution may be varied by adding various acids or bases. For example, the pH of the solution may be increased by adding sodium bicarbonate, sodium hydroxide, or other base to the solution. The pH of the solution may be decreased by adding an acid such as hydrochloric acid, acetic acid, or other acid to the solution.
The synthesis of the hydrophilic portion 102 may be carried out at room temperature. In some embodiments, the reaction solution may be heated to increase a reaction rate of formation of the hydrophilic portion 102 of the amphiphilic nanoparticles 100. In other embodiments, the reaction rate may be increased by microwave irradiation. The reaction may proceed for between about one minute and several hours. In some embodiments, the size of the hydrophilic portion 102 may be increased by increasing the synthesis time of forming the hydrophilic portion 102. In embodiments where the hydrophilic portion 102 is formed by hydrolysis, the reaction may leave one or more exposed hydroxyl groups on the hydrophilic portion 102. The hydrophilic portion 102 may include one or more additional functional groups, such as additional hydroxyl groups, a carboxyl group, a carbonyl group, an amino group, a thiol group, and a phosphate group.
The hydrophilic precursor may be hydrolyzed to form a plurality of hydrophilic precursors with exposed hydroxyl groups. The exposed hydroxyl groups of the hydrophilic precursors may react with each other in a condensation reaction, forming the hydrophilic portion 102 including a base material and hydrophilic functional groups on a surface of the base material. The exposed functional groups may be the same functional groups as the functional groups of the hydrophilic precursor. A surface of the hydrophilic portion 102 may have the general structure as shown below, where Rn includes a hydrophilic group, and M is at least one of carbon, silicon, iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt. In embodiments where M is carbon or a metal (e.g., iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt), adjacent metal atoms may be directly bonded to each other without intervening oxygen atoms and the carbon based materials may include hydrophilic substitution (e.g., adjacent carbon atoms may be directly bonded to each other or may be connected via a hydrophilic functional group).
A hydrophobic precursor may be added to the reaction solution including the hydrophilic portion 102. An organic solvent in which the hydrophobic precursor is soluble may be added to the reaction mixture. In some embodiments, the organic solvent is a nonpolar solvent. The hydrophobic functional group of the hydrophobic precursor may be soluble in an organic phase whereas the hydrophilic functional group on the surface of the base material may be soluble in an aqueous phase.
The amphiphilic nanoparticles 100 may be formed by reacting at least some of the exposed hydroxyl groups of the hydrophilic portion 102 with one or more of the hydrophobic precursors. The hydrophobic precursor may include one or more exposed hydroxyl groups. In some embodiments, the hydrophobic precursor is hydrolyzed to create exposed hydroxyl groups on the hydrophobic precursor.
In some embodiments, the hydrophobic portion 104 grows from one end of the hydrophilic portion 102. Without being bound by any theory, it is believed that only a portion of the hydrophilic portion 102 contacts the nonpolar solvent in which the hydrophobic precursors are dissolved because of the insolubility of the hydrophilic portion 102 in the nonpolar solvent. The hydroxyl groups of a portion of the hydrophilic portion 102 that contacts the hydrophobic precursor (e.g., at an interface between the nonpolar solvent and the polar solvent of the hydrophilic portion 102) may react with the hydrophobic precursors to form the hydrophobic portion 104 of the amphiphilic nanoparticle 100. An exposed surface of the hydrophobic portion 104 may have a general structure as shown below, where Rm includes a hydrophobic functional group, and M is at least one of carbon, silicon, iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt. In embodiments where M is a metal (e.g., iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt), adjacent metal atoms may be directly bonded to each other without intervening oxygen atom.
The amphiphilic nanoparticle 100 may include one or more exposed hydrophobic, nonpolar organic groups from the hydrophobic precursor, and one or more functional groups (e.g., hydroxyl, carboxyl, carbonyl, amino, thiol, phosphate, a metal, a metal oxide) from the hydrophilic precursor.
The hydrophobic precursor may include an oxysilane including a nonpolar, organic component. The hydrophobic precursor may include at least one central atom such as carbon, silicon, iron, titanium, germanium, tin, lead, zirconium, ruthenium, nickel, and cobalt, one or more hydrocarbon groups bonded to the central atom, and one or more alkoxy groups bonded to the central atom. In other embodiments, the hydrophobic precursor includes a hydrocarbon bonded to an isocyanate functional group (—N═C═O), such as octadecyl isocyanate. In some embodiments, the hydrocarbon group is an alkyl such as methyl, ethyl, propyl, butyl, pentyl, hexyl, octyl, dodecyl, and/or octadecyl groups, an aikaryl group such as benzyl groups attached via the aryl portion (e.g., 4-methylphenyl, 4 hydroxymethylphenyt or 4-(2-hydroxyethyl)phenyl, and/or aralkyl groups attached at the benzylic (alkyl) position, such as in a phenylmethyl and 4-hydroxyphenylmethyl groups, and/or attached at the 2-position, such as in a phenethyl and 4-hydroxyphenethyl groups); lactone groups, imidazole, and pyridine groups. In some embodiments, the alkoxy group is a methoxy group, an ethoxy group, a propoxy group, or a butoxy group. The hydrophobic precursors may include alkyloxysilanes, such as trialkoxysilanes including trimethoxysilane, isobutyltriethoxysilane, isobutyltrimethoxysilane, vinyitrimethoxysilane, hexadecyltrimethoxysilane (HDTMOS), methyltrimethoxysilane, ethyltrimethoxysilane, octyltrimethoxysilane, octyltriethoxysilane, or other oxysilanes.
The hydrophobic precursor may include a compound configured to form hydrophobic functional groups on a surface of the amphiphilic nanoparticle 100. In some embodiments, a hydroxyl group of the alcohol or the hydrophobic precursor may react with an exposed hydroxyl group on the base of the amphiphilic nanoparticle in a condensation reaction to form the hydrophobic portion 104. By way of non-limiting example, a hydrophobic precursor may react with an exposed hydroxyl group on a carbon-containing material to form the hydrophobic portion 104. In other embodiments, a hydroxyl group of the hydrophobic precursor may react with exposed hydroxyl groups of the hydrophilic portion 102 in a condensation reaction to form the hydrophobic portion 104. By way of example only, the hydrophobic precursor may include an alcohol having the general formula RR′R″—OH, where R, R′, and R″ may include hydrogen, or an organic group, such as an alkyl group, alkenyl group, alkynyl group, aryl group, etc. The alcohol may include one or more hydroxyl groups (e.g., a diol, triol, etc.). The hydrophobic portion 104 may be formed on only one side of the amphiphilic nanoparticle 100 (e.g., an opposite side as the hydrophilic portion 102).
The hydrophobicity of the hydrophobic portion 104 may be controlled by altering the number of functional groups and the size of the functional groups of the hydrophobic precursor. In some embodiments, the hydrophobicity of the hydrophobic portion 104 is increased by increasing the carbon content of the functional group of the hydrophobic precursor. For example, ethyltrimethoxysilane may be more hydrophobic than methyltrimethoxysilane. Similarly, hexadecyltrimethoxysilane may be more hydrophobic than ethyltrimethoxysilane. The hydrophobicity of the amphiphilic nanoparticles 100 may also be increased by increasing a concentration of the hydrophobic functional group relative to a concentration of the hydrophilic functional group in the reaction mixture or by decreasing a reaction time of forming the hydrophilic portion 102 relative to a reaction time of forming the hydrophobic portion 104. In yet other embodiments, where the base includes a carbon-containing material, the hydrophobic portion 104 of the amphiphilic nanoparticle 100 may be the core and the hydrophilic portions 102 may be any hydrophilic functional groups attached to the carbon-containing material.
The amphiphilic nanoparticles 100 may be removed from the reaction solution by centrifugation, ultrafiltration, or combinations thereof. In some embodiments, the amphiphilic nanoparticles 100 are recovered by flowing the solution through a membrane filter. The filter may have a pore size ranging from between about 10 nm and about 1,000 nm, such as between about 10 nm and about 100 nm, between about 100 nm and about 200 nm, between about 200 nm and about 400 nm, or between about 400 nm and about 1,000 nm. In some embodiments, the solution is flowed through a filter having a pore size of between about 200 nm and about 400 nm. The resulting solid residue may be dried and collected. The solid residue may include amphiphilic nanoparticles 100 with a hydrophilic portion 102 and a hydrophobic portion 104. The hydrophobic portion 104 may be opposite the hydrophilic portion 102 such that one portion of the amphiphilic nanoparticle 100 is attracted to and soluble in a hydrocarbon phase and another portion of the amphiphilic nanoparticle 100 is attracted to and soluble in an aqueous phase.
The amphiphilic nanoparticles 100 may have a size distribution ranging from between about 10 nm and about 1,000 nm. In some embodiments, the size distribution may correspond to the size of the filter through which the solution was passed to separate the nanoparticles from the reaction solution. The amphiphilic nanoparticles 100 may be monodisperse wherein each of the amphiphilic nanoparticles 100 has substantially the same size, shape, and material composition, or may be polydisperse, wherein the amphiphilic nanoparticles 100 include a range of sizes, shapes, and/or material composition. In some embodiments, each of the amphiphilic nanoparticles 100 has substantially the same size and the same shape as each of the other amphiphilic nanoparticles 100.
The amphiphilic nanoparticles 100 may stabilize an emulsion at higher temperatures than a typical surfactant. For example, typical surfactants may degrade or otherwise lose functionality at temperatures in excess of about 250° C. However, the amphiphilic nanoparticles 100 described herein may be stable at high temperatures that may be encountered within a subterranean formation. For example, the amphiphilic nanoparticles 100 may be stable at temperatures up to about 500° C. In some embodiments, the amphiphilic nanoparticles 100 are exposed to a temperature between about 250° C. and about 500° C., such as between about 300° C. and about 400° C., or between about 400° C. and about 500° C., and may remain stable.
The amphiphilic nanoparticles 100 may remain effective at stabilizing an emulsion at higher salinity concentrations than typical surfactants. Due to the presence of the functional groups on the amphiphilic nanoparticles 100, the amphiphilic nanoparticles 100 may be repelled from the salts of a brine solution, whereas non-functionalized particles may tend to agglomerate or gel with a salt.
The amphiphilic nanoparticles 100 may be stable within a wide pH range. For example, the amphiphilic nanoparticles 100 may be formulated to be stable at a pH between about 3.0 and about 12.0. In some embodiments, the amphiphilic nanoparticles 100 are formulated to be stable at a pH as high as about 12.0 by forming the amphiphilic nanoparticles 100 from anionic functional groups such as hydroxyl groups, carboxylate groups, carboxyl groups, sulfate groups, phosphate groups, or other anionic groups. In other embodiments, the amphiphilic nanoparticles 100 are formulated to be stable at a pH as low as about 3.0 by including terminal ends of cationic groups such as amine groups.
The amphiphilic nanoparticles 100 may stabilize an emulsion in any application where a stable emulsion is desired. For example, the amphiphilic nanoparticles 100 may be used in water flooding applications or floatation cell applications. The amphiphilic nanoparticles 100 may stabilize an emulsion by themselves, or the amphiphilic nanoparticles 100 may be used with one or more surfactants.
Referring to
The suspension formation process 200 may include forming a suspension including amphiphilic nanoparticles and at least one carrier fluid. The at least one carrier fluid may, fir example, comprise water, or a brine solution. As used herein, the term “suspension” means and includes a material including at least one carrier fluid in which amphiphilic nanoparticles are substantially uniformly dispersed. The suspension may be a flooding suspension used, such as used in water flooding of a subterranean formation during enhanced oil recovery processes. The amphiphilic nanoparticles of the flooding suspension may be compatible with other components (e.g., materials, constituents, etc.) of the flooding suspension. As used herein, the term “compatible” means that a material does not impair the functionality of the amphiphilic nanoparticles or cause the amphiphilic nanoparticles to lose functionality as surfactants and emulsion stabilizers.
The flooding suspension may be formulated to include a concentration of the amphiphilic nanoparticles ranging from between about 50 ppm to about 50,000 ppm. For example, in some embodiments, the flooding suspension may have a concentration of amphiphilic nanoparticles ranging from between about 50 ppm and about 500 ppm, between about 500 ppm and about 1,000 ppm, between about 1,000 ppm and about 5,000 ppm, or above 5,000 ppm. In some embodiments, the flooding suspension may have a concentration ranging from between about 50 ppm to about 5,000 ppm. In some embodiments, the suspension includes a portion of amphiphilic nanoparticles with a carbon-based core and another portion of amphiphilic nanoparticles with another base portion. By way of example, the suspension may include a first portion of amphiphilic nanoparticles including a carbon-containing material, a second portion of amphiphilic nanoparticles including a silica core, and a third portion of amphiphilic nanoparticles including a metal core. The emulsion may have the same, a higher, or a lower concentration of amphiphilic nanoparticles than the flooding suspension.
With continued reference to
The pH of the flooding suspension may be altered to control the solubility of the amphiphilic nanoparticles within the flooding suspension. For example, where the amphiphilic nanoparticles include cationic functional groups (e.g., amino groups), decreasing the pH of the flooding suspension may increase the solubility of the amphiphilic nanoparticles in the aqueous flooding suspension. Where the amphiphilic nanoparticles include anionic functional groups (e.g., hydroxyl, carboxyl, carbonyl, phosphate, thiol groups, etc.), increasing the pH of the flooding suspension may increase the solubility of the amphiphilic nanoparticles in the flooding suspension. Altering the pH of the flooding suspension may alter the surface charge of the amphiphilic nanoparticles. For example, increasing a pH of a flooding suspension including anionic amphiphilic nanoparticles may increase the net charge of the anionic amphiphilic nanoparticles in the flooding suspension. Decreasing a pH of a flooding suspension including cationic amphiphilic nanoparticles may increase the net charge of the cationic amphiphilic nanoparticles.
After the flooding suspension is introduced into the subterranean formation, the pH of the flooding suspension may be altered to reduce the solubility of the amphiphilic nanoparticles in the aqueous phase of the flooding suspension. For example, where the amphiphilic nanoparticles include cationic functional groups, the pH of the flooding suspension may be reduced to cause the amphiphilic nanoparticles to move to the interface between the aqueous phase and the hydrocarbon phase. In some embodiments, the pH may be reduced to below about 7.0, such as below 5.0, below 4.0, or below 3.0. Where the amphiphilic nanoparticles comprise anionic functional groups, the pH of the flooding suspension may be increased to cause the amphiphilic nanoparticles to move to the interface between the aqueous phase and the hydrocarbon phase. In some embodiments, the pH may be increased to above 7.0, such as above 8.0, above 9.0, above 10.0, and up to 12.0.
The amphiphilic nanoparticles are structured and formulated to facilitate a formation of a stabilized emulsion of a hydrocarbon material and an aqueous material. For example, the amphiphilic nanoparticles may be structured and formulated to gather (e.g., agglomerate) at, adhere to, and/or adsorb to interfaces of a hydrocarbon material and an aqueous material to form a Pickering emulsion comprising units (e.g., droplets) of one of the hydrocarbon material and the aqueous material dispersed in the other of the hydrocarbon material and the aqueous material. The amphiphilic nanoparticles may prevent the dispersed material (e.g., the hydrocarbon material or the aqueous material) from coalescing, and may thus maintain the dispersed material as units throughout the other material.
The extraction process 204 may include flowing (e.g., driving, sweeping, forcing, etc.) the stabilized emulsion from the subterranean formation to the surface. The amphiphilic nanoparticles prevent the dispersed material from coalescing and enable substantial removal of hydrocarbons from the subterranean formation.
Once the hydrocarbons are removed from the subterranean formation, at least a portion of the emulsion may be destabilized in the emulsion destabilization process 206 to form distinct, immiscible phases including an aqueous phase and a hydrocarbon phase. One or more properties (e.g., temperature, pH, material composition, pressure, etc.) of the stabilized emulsion or the aqueous phase may be modified (e.g., altered, changed) to a least partially destabilize the emulsion. For example, the pH of the aqueous phase may be modified to increase the solubility of the amphiphilic nanoparticles within the aqueous phase, thereby destabilizing the emulsion and forming distinct, immiscible phases.
In some embodiments, the pH of the emulsion or the aqueous phase may be altered to cause the amphiphilic nanoparticles to move into the aqueous phase and destabilize the emulsion. Where the amphiphilic nanoparticles comprise anionic functional groups, the pH of the aqueous phase may be increased to increase the solubility of the amphiphilic nanoparticles in the aqueous phase. The pH of the aqueous phase may be increased by adding a base, such as a hydroxide (e.g., sodium hydroxide) or a bicarbonate (e.g., sodium bicarbonate) to the aqueous phase. Where the amphiphilic nanoparticles comprise cationic functional groups, the pH of the aqueous phase may be reduced to increase the solubility of the amphiphilic nanoparticles in the aqueous phase. The pH of the aqueous solution may be decreased by adding hydrochloric acid, phosphoric acid, and acetic acid, or another acid to the aqueous solution.
A demulsifier may be added to the emulsion to destabilize the emulsion and form distinct, immiscible phases including an aqueous phase and a hydrocarbon phase. In some embodiments, the emulsion is destabilized by adjusting the pH of at least one of the aqueous phase and the emulsion and by adding a demulsifier to the emulsion.
Referring to
The suspension formation process 300 may include forming a suspension including the amphiphilic nanoparticles and at least one carrier fluid. The carrier fluid may, for example, comprise water, a brine solution, or a caustic soda (NaOH) solution. The suspension may be formulated to include a concentration of amphiphilic nanoparticles similar to the flooding suspension described above with reference to
The mixing process 302 may include mixing the suspension with a slurry including a bituminous sand and water to form a stabilized emulsion. The slurry may include hot water, caustic soda, and the bituminous sand. The transportation process 304 may include hydrotransporting the slurry to a location where the stabilized emulsion may be processed to remove hydrocarbons therefrom (e.g., from the bituminous sand). In some embodiments, the mixing process 302 may be performed simultaneously with the transportation process 304. In some embodiments, a pH of the slurry may be adjusted to reduce the solubility of the amphiphilic nanoparticles in a hydrophilic portion of the slurry and increase the solubility of the amphiphilic nanoparticles in the stabilized emulsion during the mixing process and the transportation process 304.
The amphiphilic nanoparticles are structured and formulated to facilitate a formation of a stabilized emulsion of a hydrocarbon material and an aqueous phase. For example, the amphiphilic nanoparticles may be structured and formulated to gather at, adhere to, and/or adsorb to interfaces of the hydrocarbon material and the aqueous material to form a Pickering emulsion comprising units (e.g., droplets) of one of the hydrocarbon material and the aqueous material in the other of the hydrocarbon material and the aqueous material.
The extraction process 306 may include extracting hydrocarbons from the stabilized emulsion. In some embodiments, the extraction process 306 includes extracting hydrocarbons from the stabilized emulsion of the slurry in a floatation process.
After the hydrocarbons are removed from the aqueous phase in the floatation process, at least a portion of the stabilized emulsion may be destabilized in the emulsion destabilization process 308 to form distinct, immiscible phases including an aqueous phase and a hydrocarbon phase. One or more properties (e.g., temperature, pH, material composition, pressure, etc.) of the stabilized emulsion or the aqueous phase may be modified (e.g., altered, changed) to a least partially destabilize the emulsion. For example, the pH of the aqueous phase may be modified to increase the solubility of the amphiphilic nanoparticles within the aqueous phase, thereby destabilizing the emulsion and forming distinct, immiscible phases. The pH of the stabilized emulsion may be altered to cause the amphiphilic nanoparticles to move into the aqueous phase and destabilize the emulsion, as described above with reference to emulsion destabilization process 206 of
After the emulsion is destabilized, the hydrocarbon material may be separated from the aqueous material and recovered. Thereafter, the amphiphilic nanoparticles may be recovered from the aqueous phase. In some embodiments, the pH of the aqueous solution may be adjusted to reduce the solubility of the amphiphilic nanoparticles in the aqueous solution and precipitate the amphiphilic nanoparticles from the aqueous solution. For example, where the amphiphilic nanoparticles include functional groups such as amine functional groups, decreasing the pH of the aqueous material may reduce the solubility of the amphiphilic nanoparticles in the aqueous solution, thereby causing them to precipitate out of the aqueous solution. In embodiments where the functional group of the amphiphilic nanoparticles are hydroxyl, carboxyl, carbonyl, thiol, phosphate, or other anionic groups, increasing the pH of the aqueous solution may cause the amphiphilic nanoparticles to precipitate out of the aqueous solution. In other embodiments, the amphiphilic nanoparticles are recovered by filtering the aqueous solution through a filter. The filter may have a pore size ranging from between about 10 nm and about 5,000 nm, depending on the size of the amphiphilic nanoparticles. In some embodiments, more than one filtration step may be performed. For example, a first filtration step may filter out sands and other solid particles having a larger diameter than the amphiphilic nanoparticles. Thereafter, the amphiphilic nanoparticles may be separated from the aqueous solution.
While the disclosure is susceptible to various modifications and alternative forms, specific embodiments have been shown by way of example in the drawings and have been described in detail herein. However, the disclosure is not intended to be limited to the particular forms disclosed. Rather, the disclosure is to cover all modifications, equivalents, and alternatives falling within the scope of the disclosure as defined by the following appended claims and their legal equivalents.
This application is a continuation-in-part of U.S. patent application Ser. No. 14/169,432, filed Jan. 31, 2014, the disclosure of which is hereby incorporated herein in its entirety by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14169432 | Jan 2014 | US |
| Child | 14519728 | US |
