Patent Application
20160068743
The present invention relates to the field of oil extraction. The invention relates more specifically to improving the recovery rate in hydrocarbon reservoirs.
Whereas, at the start of exploitation of an oil deposit, the natural pressure of the hydrocarbons in the reservoir is generally sufficient to ensure their movement toward the production wells during the “primary recovery” phase, this natural pressure decreases in the course of the exploitation and it then becomes necessary to use more active recovery methods. In a first stage, an aqueous phase is introduced into the reservoir, via injection wells, and, when it comes into contact with the hydrocarbons, it promotes their movement toward the production wells. However, the introduction of water alone allows only a very partial extraction of the hydrocarbons.
Various techniques are known for recovering hydrocarbons when water entrainment alone is not sufficient for extraction. To increase the rate of extraction out of carbon reservoirs, it has especially been proposed to inject extraction fluids comprising associative polymers which give the fluid high viscosity. Such fluids may be used in techniques known as “polymer flooding” for entraining the hydrocarbons out of the reservoir more efficiently than a simple aqueous composition. More specifically, use may be made of extraction fluids based on associative polymers for inducing in the reservoir a relative permeability modification (RPM), which induces a preferential movement of the hydrocarbons at the expense of the water. RPM techniques generally consist in using the polymers at concentrations that induce not only an increase in viscosity, but also a gelation of non-productive zones in which only water is present.
The injection of extraction fluids of the abovementioned type, which are highly viscous, into hydrocarbon reservoirs generally involves the use of high pressures, which, on the one hand, involve energy expenditures, and, on the other hand, may degrade the polymers under the effect of the shear.
One objective of the present invention is to provide extraction fluids based on viscosifying polymers which have efficiency similar to that of the known fluids, but which are more easily injectable, making it possible, inter alia, to reduce the energy necessary for their injection, and for which the degradation of the viscosifying polymers under shear are preferably reduced or even zero.
For this purpose, a novel type of extraction fluid is proposed according to the present invention, which comprises, in an aqueous medium:
More specifically, according to a first aspect, one subject of the present invention is an extraction fluid comprising, in an aqueous medium:
According to another aspect, the invention relates to the use of the abovementioned fluids as extraction fluids. In this context, one subject of the invention is in particular a process for recovering hydrocarbons in a hydrocarbon reservoir, comprising a step in which an extraction fluid of the abovementioned type is injected into a hydrocarbon reservoir in which the temperature and/or pH conditions are suitable for lyzing all or some of the labile surfactant. According to a first embodiment, the extraction fluid is used in polymer flooding mode, i.e. to supply to the reservoir a fluid of high viscosity that is capable of efficiently entraining the hydrocarbons. Alternatively, the extraction fluid may be used in permeability modification mode, i.e. to bring about gelation of the less productive zones of the reservoir and thus limit the production of water.
The expression “associative polymer” is understood, within the meaning of the present description, to be a polymer suitable for increasing the viscosity of an aqueous medium by associations that involve hydrophobic-hydrophobic interactions between the polymers. Such polymers are also sometimes denoted by the name “hydrophobically associative water-soluble polymers” (HAPs) or else “amphiphilic polymers”. These are, in general, polymers comprising a backbone of hydrophilic nature and that include, along the chains and/or at all or some of the ends thereof, small amounts (typically of the order of 0.001 mol % to 10 mol %, and generally a few molar percent at the very most) of functions of hydrophobic nature. When such polymers are placed in an aqueous medium, they form, in a manner known per se, hydrophobic connections (the hydrophobic functions group together in order to reduce the energy of the system, in the same way as surfactant micelles are formed in an aqueous medium).
Furthermore, the concept of “labile surfactant” (or “cleavable surfactant”) denotes here a surfactant which is suitable for being lyzed, typically by being cleaved into two separate molecules, under pH and temperature conditions in which at least one portion of the associative polymers with which it is associated in the composition is not degraded. The cleavable surfactants used according to the invention are surfactants which degrade after injection, under conditions where the associative polymers are not degraded. Labile surfactants of this type are well known in the literature. For further details, reference may especially be made to “Cleavable surfactants” Alireza Tehrani-Bagha, Krister Holm.
The specific use of a labile surfactant gives the extraction fluid according to the invention the advantages of the known extraction fluids while being free of their drawbacks. Specifically, due to the presence of this labile surfactant, the extraction fluid has, when it is injected, a reduced viscosity which facilitates its injection, and the viscosity is re-established in the hydrocarbon reservoir in the zone where it is desired to perform the extraction.
The lowering of the viscosity obtained owing to the presence of the labile surfactant makes it possible to substantially reduce the pressure loss phenomena and, in the case where polymers sensitive to degradation are used, enables a reduction in the degradation of the polymers under shear.
Furthermore, the nature of the associative polymers present in the extraction fluids of the present invention is highly adjustable.
In particular, according to an advantageous embodiment, the extraction fluids of the invention may advantageously comprise, as associative polymers, amphiphilic polymers of relatively low molecular weight (for example less than 1 000 000 g/mol, or even less than 500 000 g/mol, for example less than 100 000 g/mol) that make it possible to induce high viscosities after lysis of the labile surfactant, and do so starting from relatively low concentrations, and which are in addition less sensitive to shear degradation than polymers of larger size.
In practice, any associative polymer may be used according to the invention. On this subject, it should be noted that, in addition to the aforementioned advantages, the labile surfactant present in the compositions of the invention makes it possible to improve the hydration of the polymers in an aqueous medium, which makes it possible to use any type of associative polymer, including those that are reputedly the least hydratable, in the compositions of the invention. The invention thus opens the way to the use of numerous amphiphilic polymers in extraction liquids.
Considering the wide range of polymers and surfactants that may be used in the context of the invention, the extraction method described here is extremely adjustable. By making a suitable choice of polymer and of surfactant, it is possible to provide, according to the invention, both extraction fluids for which a high viscosity will be obtained (recovered) after a few meters only and fluids for which the viscosity remains low up to the extraction zone.
It is possible to finely adjust the behavior of the extraction fluid in order to adapt the change in its viscosity along the injection zone. As a function of the polymer and surfactant used, it is within the abilities of a person skilled in the art to adapt the concentrations of the two compounds in order to obtain the desired viscosity change profile. Before the lysis of the labile surfactants, the associative polymers and the surfactants interact according to a known mechanism, described in particular in “Interactions between hydrophobically modified polymers and surfactants” B. Magny, I. Iliopoulos, R. Audebert, L. Piculell, B. Lindman Progress in Colloid & Polymer Science Volume 89, 1992, pp. 118-121.
The interactions between associative polymers and surfactants vary in a manner known per se as a function of the surfactant content. When a very small amount of surfactant is added, this small amount of surfactant densifies the number of hydrophobic bonds, which increases the viscosity. At a low surfactant content, the viscosity thus increases up to a maximum as the surfactant is added. Beyond the limit content of surfactant for which this maximum is observed, the tendency reverses and the addition of surfactant on the contrary makes the interactions between the polymers, and therefore the viscosity, decrease more and more. For any surfactant and polymer pair, there is a minimum surfactant concentration beyond which a systematic decrease in the viscosity is obtained, this minimum concentration being very easy to determine.
According to one embodiment, the surfactant and the polymer and also the respective concentrations thereof are chosen so that a low viscosity is maintained from the surface to the zone where it is desired to carry out the extraction (especially polymer flooding or RPM) and the rise in viscosity due to the lysis of the surfactant preferably takes place just at the extraction zone.
In addition to the abovementioned advantages, the associative polymers used in the extraction fluids of the invention have the advantage of being able to be used in the presence of salts (the presence of salts moreover generally improves their associative nature), which allows the use of the water immediately available in the environment close to the extraction zone without having to worry about its purity or its salt content. Thus, in particular, the invention lends itself well to the formulation of extraction fluids based on seawater or on production water and more generally on any water that may contain salts (including at high contents that may range up to 25% by mass and/or with high hardnesses that may range up to Mg2+ and Ca2+ contents of the order of 5000 ppm): according to a particular embodiment, the fracturing fluid of the invention comprises seawater or production water as the aqueous medium.
Various more particular features and embodiments of the invention will now be described in greater detail.
The polymers used according to the invention may vary to quite a large extent.
They may, for example, be selected from the polymers described in U.S. Pat. No. 4,529,523, U.S. Pat. No. 4,432,881, U.S. Pat. No. 4,814,096, WO 85/03510, U.S. Pat. No. 4,702,319, U.S. Pat. No. 4,709,759, U.S. Pat. No. 4,638,865, U.S. Pat. No. 4,780,517, U.S. Pat. No. 4,852,652 or U.S. Pat. No. 4,861,499.
More generally, they may be associative polymers based on a hydrophilic backbone bearing hydrophobic groups of the type obtained by synthesis pathways of HASE type (direct synthesis pathway) or of HEUR type (post-addition of hydrophobic groups to a hydrophilic chain). Examples of this type of synthesis are in particular described in Prog. Color Colorants Coat. Vol. 4, pp. 71-77 (2011).
Use may furthermore be made of associative polymers resulting from micellar radical polymerization processes of the type described in U.S. Pat. No. 4,432,881 or else in Polymer, vol. 36, No. 16, pp. 3197-3211 (1996), to which reference may be made for further details, by copolymerization of hydrophilic monomers and hydrophobic monomers within an aqueous dispersant medium (typically water or a water/alcohol mixture) which comprises:
According to one particular embodiment, the hydrophobic monomers present in surfactant micelles used in micellar polymerization may be monomers which, by themselves, have the property of forming micelles without needing to add additional surfactants (monomers referred to as being “self-micellizable” in the rest of the description). According to this particular embodiment, the surfactant used may be the self-micellizable hydrophobic monomer itself, used without other surfactant, although the presence of such an additional surfactant is not excluded. Thus, for the purposes of the present description, when mention is made of hydrophobic monomers in surfactant micelles, this notion encompasses both (i) hydrophobic monomers present in surfactant micelles other than these monomers, and (ii) monomers comprising at least one hydrophobic part or block and forming by themselves the micelles in aqueous medium. The two aforementioned embodiments (i) and (ii) are compatible and may coexist (hydrophobic monomers in micelles formed by another self-micellizable monomer for example, or else micelles comprising a combination of surfactants and self-micellizable monomers).
In micellar polymerization, the hydrophobic monomers contained in the micelles are said to be in “micellar solution”. The micellar solution to which reference is made is a micro-heterogeneous system that is generally isotropic, optically transparent and thermodynamically stable.
According to an advantageous embodiment, the associative polymers used according to the present invention are polymers obtained according to a preparation process that comprises a step (E) of micellar radical polymerization in which the following are placed in contact, in an aqueous medium (M):
The aqueous medium (M) used in step (E) is a medium comprising water, preferably in a proportion of at least 50% by mass, or even at least 80%, for example at least 90%, or even at least 95%. This aqueous medium may optionally comprise solvents other than water, for example a water-miscible alcohol. Thus, the medium (M) may be, for example, an aqueous-alcoholic mixture. According to one possible variant, the medium (M) may comprise other solvents, preferably in a concentration in which said solvent is water-miscible, which may especially make it possible to reduce the amount of stabilizing surfactants used. Thus, for example, the medium (M) may comprise pentanol, or any other additive for adjusting the aggregation number of the surfactants. In general, it is preferable for the medium (M) to be a continuous phase of water consisting of one or more solvents and/or additives that are miscible with each other and in water in the concentrations at which they are used.
For the purposes of the present description, the term “radical polymerization control agent” means a compound that is capable of extending the lifetime of the growing polymer chains in a polymerization reaction and of giving the polymerization a living or controlled nature. This control agent is typically a reversible transfer agent as used in controlled radical polymerizations denoted by the terminology RAFT or MADIX, which typically use a reversible addition-fragmentation transfer process, such as those described for example in WO 96/30421, WO 98/01478, WO 99/35178, WO 98/58974, WO 00/75207, WO 01/42312, WO 99/35177, WO 99/31144, FR 2794464 or WO 02/26836.
According to one advantageous embodiment, the radical polymerization control agent used in step (E) is a compound which comprises a thiocarbonylthio group —S(C═S)—. Thus, for example, it may be a compound which comprises a xanthate group (bearing —SC═S—O— functions), for example a xanthate. A suitable xanthate is Rhodixan A1 available from Solvay. Other types of control agent may be envisioned (for example of the type used in CRP or ATRP).
According to one particular embodiment, the control agent used in step (E) may be a polymer chain derived from a controlled radical polymerization and bearing a group that is capable of controlling a radical polymerization (polymer chain of “living” type, which is a type that is well known per se). Thus, for example, the control agent may be a polymer chain (preferably hydrophilic or water-dispersible) functionalized at the chain end with a xanthate group or more generally comprising a group —SC═S—, for example obtained according to the MADIX technology.
Alternatively, the control agent used in step (E) is a non-polymeric compound bearing a group that ensures the control of the radical polymerization, especially a thiocarbonylthio group —S(C═S)—.
According to one particular variant, the radical polymerization control agent used in step (E) is a polymer, advantageously an oligomer, of water-soluble or water-dispersible nature and bearing a thiocarbonylthio group —S(C═S)—, for example a xanthate group —SC═S—O—. This polymer, which is capable of acting both as a polymerization control agent and as a monomer in step (E), is also referred to as a “prepolymer” in the rest of the description. Typically, this prepolymer is obtained by radical polymerization of hydrophilic monomers in the presence of a control agent bearing a thiocarbonylthio group —S(C═S)—, for example a xanthate. Thus, for example, according to one advantageous embodiment which is illustrated at the end of the present description, the control agent used in step (E) may advantageously be a prepolymer bearing a thiocarbonylthio group —S(C═S)—, for example a xanthate group —SC═S—O—, obtained at the end of a step (E0) of controlled radical polymerization prior to step (E). In this step (E0), the following may typically be placed in contact: hydrophilic monomers, advantageously identical to those used in step (E); a radical polymerization initiator; and a control agent bearing a thiocarbonylthio group —S(C═S)—, for example a xanthate.
The use of the abovementioned step (E0) prior to step (E) makes it possible, schematically, to hydrophilize a large number of control agents bearing thiocarbonylthio functions (for example xanthates, which are rather hydrophobic by nature), by converting them from prepolymers that are soluble or dispersible in the medium (M) of step (E). Preferably, a prepolymer synthesized in step (E0) has a short polymer chain, for example comprising a sequence of less than 50 or less than 25 monomer units, for example between 2 and 15 monomer units.
Unexpectedly, it turns out that the conditions of step (E) make it possible to combine the advantages both of controlled radical polymerization and of micellar polymerization. Within this context, the inventors have in particular now demonstrated that the presence of micelles in the polymerization medium does not affect the action of the control agents, which make it possible to perform a controlled polymerization of the monomers present in the aqueous medium in a similar manner to a controlled radical polymerization performed in homogeneous medium, thus making it possible very readily to predict and control the average molar mass of the synthesized polymer (this mass is proportionately higher the lower the initial concentration of control agent in the medium, this concentration dictating the number of growing polymer chains). At the same time, the presence of the control agent is not detrimental either to the advantageous effect observed in polymerization, namely the precise control of the size of the hydrophobic blocks.
In addition to this control of the polymerization of the monomers, not obtained in the more usual micellar polymerization processes, the use of step (E) of the process of the invention in addition makes it possible, also completely surprisingly, to attain polymers having both a large and controlled size, which proves very particularly unexpected in view of the maximum sizes that it is known to obtain today using controlled radical polymerization or micellar radical polymerization methods in the absence of control agents.
Under the conditions of step (E), it proves possible to control the number-average molar mass of the polymers which makes it possible, inter alia, to produce polymers having low masses.
According to one advantageous embodiment, the associative polymer present in the fracturing fluid of the invention is synthesized according to the aforementioned step (E) and has a mass of between 50 000 and 10 000 000, preferably of between 750 000 and 5 000 000 g/mol, in particular between 1 000 000 and 4 000 000 g/mol. Typically, such polymers may be used at a concentration below their critical overlap concentration. On account of their small sizes, such polymers can diffuse at the interfaces and participate in modifying the properties of these interfaces or surfaces.
Irrespective of its nature, the associative polymer of the extraction fluids according to the invention is typically present:
The labile surfactants used within the context of the invention are surfactants which have groups that have an affinity for the hydrophobic groups present on the associative polymers and moreover for the hydrophilic chains. Advantageously, they are water-soluble surfactants.
Furthermore, they are compounds bearing a cleavable function. This cleavable function is advantageously an ester function.
According to one embodiment, the labile surfactants present in the fracturing fluids of the invention are non-ionic surfactants. They may also be surfactants that have the structure of non-ionic surfactants, but that optionally bear a functionalized, optionally charged, group at the chain end.
According to an advantageous variant, these labile surfactants comprise ethoxylated fatty acid esters, typically corresponding to the formula R—COO—(CH2—CH2—O—)n—H, where R is a linear or branched, preferably linear, hydrocarbon-based chain, typically an alkyl comprising from 4 to 22 carbon atoms, for example 5 to 18 carbon atoms; and n is greater than 3, n ranging for example from 4 to 50.
One surfactant well-suited to the invention is for example Alkamuls PSML20 (also referred to as Polysorbate 20), of the following formula:
This compound is available from Solvay.
pH Control Agent(s)
In this type of application (RPM), the interactions between the associative polymers, which form a gel in a water-rich medium, are disrupted or even broken in the presence of large amounts of hydrocarbons.
As a result, during the implementation of the invention, when an extraction fluid is used for gelling the less productive zones of the reservoir, these gelled zones are not completely blocked: admittedly, they do immobilize the water by promoting the movement of the fluids in other zones of the reservoir, but they do not constitute an impassable barrier for the hydrocarbons.
On the contrary, the gelled zones have an oil permeability that is not reduced by the use of the associative polymers.
In other words, the invention makes it possible to ensure selectivity in the reservoir by promoting the passage of the oil at the expense of that of the water.
The invention will now be illustrated by the example given below.
29.3 g of a 30% SDS solution, 89.03 g of distilled water and 1.66 g of lauryl methacrylamide (LMA monomer) were introduced into a 500 ml round-bottomed flask at room temperature (20° C.). The mixture was stirred using a magnetic stirrer bar for 6 hours, until a clear micellar solution was obtained.
32.9 g of the micellar solution thus prepared, 7.53 g of water, 40.7 g of acrylamide (aqueous solution at 50% by mass), 32 g of AMPS (aqueous solution at 51% by mass), 0.454 g of Rhodixan A1 (ethanolic solution at 1.0% by mass) and 6.00 g of ammonium persulfate (aqueous solution at 0.67% by mass) were introduced into a 250 ml round-bottomed flask at room temperature (20° C.).
The mixture was degassed by sparging with nitrogen for 20 minutes.
1.5 g of sodium formaldehyde sulfoxylate, in the form of an aqueous solution at 0.13% by mass, were added to the medium, in a single portion.
The mixture was degassed by sparging with nitrogen for 15 minutes.
The polymerization reaction was then left to proceed with stirring for 16 hours at room temperature (20° C.).
The polymer prepared above was placed in solution at 0.5% by mass of polymer in an aqueous solution of NaCl at 15% by mass in the presence of Alkamuls PSML20 labile surfactant at various concentrations.
For each of the concentrations, the viscosity of the mixture was measured at 80° C., using an AR2000 rheometer (TA Instruments, Surrey, Great Britain), equipped with a Couette-type geometry. The results are reported in the table below:
The reduction in viscosity by addition of labile surfactant is demonstrated here above 500 ppm.
The polymer from example 1 was placed in solution at 0.5 wt % in 15% NaCl in the presence of 0.5% Alkamuls PSML20. Sodium hydroxide is added in order to obtain a concentration of 83 mmol/l. The viscosity of the solution thus obtained is 10 cP at 25° C. (at 1 s−1).
The solution was placed in an oven at 80° C. for 16 h. At the end of this treatment, the viscosity of the solution was measured as equal to 4200 cP at 1 s−1 (versus 3600 cP for a polymer solution without surfactant obtained after hydration by heating for 4 h at 80° C.).
| Number | Date | Country | Kind |
|---|---|---|---|
| 1300865 | Apr 2013 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2014/057286 | 4/10/2014 | WO | 00 |
