CA1106162A - Process for reducing water influx into gas or oil producing wells - Google Patents

Process for reducing water influx into gas or oil producing wells

Info

Publication number
CA1106162A
CA1106162A CA316,441A CA316441A CA1106162A CA 1106162 A CA1106162 A CA 1106162A CA 316441 A CA316441 A CA 316441A CA 1106162 A CA1106162 A CA 1106162A
Authority
CA
Canada
Prior art keywords
water
oil
emulsion
polyacrylamide
process according
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA316,441A
Other languages
French (fr)
Inventor
Karl-Heinz Grodde
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wintershall Dea Deutschland AG
Original Assignee
Deutsche Texaco AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Deutsche Texaco AG filed Critical Deutsche Texaco AG
Application granted granted Critical
Publication of CA1106162A publication Critical patent/CA1106162A/en
Expired legal-status Critical Current

Links

Classifications

    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B33/00Sealing or packing boreholes or wells
    • E21B33/10Sealing or packing boreholes or wells in the borehole
    • E21B33/13Methods or devices for cementing, for plugging holes, crevices, or the like
    • E21B33/138Plastering the borehole wall; Injecting into the formation
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/50Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/502Oil-based compositions

Abstract

ABSTRACT OF THE DISCLOSURE
A process for reducing the influx of water into petroleum production wells by the injection thereinto of emulsions of gels of polyacrylamides or partially hydrolyzed polyacrylamides in mineral oil.

Description

~616Z

~AC~GROUND OF THE INVENTION
FIELD OF THE INVENTION
This invention relates to a process for reducing the influx of water into production wells by the injection thereinto of emulsions of gels of polyacrylamides or partially hydrolyzed polyacrylamides in mineral oil.
DESCRIPTION OF THE PRIOR ART
As the oil fields become older their flooding increases constantly. Therefore, more than ever, a search goes on in the petroleum industry for processes for an effective reduction of the influx of water into production wells. In many fields, particularly when the permeability is high, the lighter petroleum is separated off from and above the water-bearing layer. In such cases, by means of the introduction of cement into the bottom portion of the well, there is achieved a reduction of the influx of water into the well. Also, the injection of waterglass solutions, with which an electrolyte such as hydrochloric acid or ammonium chloride has been mixed, so that the thinly-flowing solution can stiffen into a stiff gel after a specific incubation period, has been proposed. With this method, however, there is a certain risk that the oil-bearing layer is also sealed off, even if both layers are separated each from the other by a packer placed at the dividing line and oil is injected into the upper layer. Such a sealing is practically impossible to avoid.
; For some years it has been recommended to use water shut-off processes with solutions of polyacrylamides or partly hydrolyzed polyacrylamides, in ~arious alternatives, and they have in fact been used on several occasions.

Polyacrylamides are long-chain polymers of acrylamide corresponding to the general formula:
( ~ C~2 ~ CH (CoNH2) ~ )n wherein n is about 50,000 or more. The molecular weight is three to six million. With partly hydrolyzed polyacrylamides a part of the amide groups - CONH2 is converted by a saponification reaction into carboxylate groups - e.g. COONa.
Particularly advantageous are polyacrylamides that are hydrolyzed to 10 - 60%, preferably in the range of 20 - 35%.
Aqueous solutions of polyacrylamides or partly hydrolyzed polyacrylamides, starting from a concentration of about 5%, behave as gels, i.e. they become plastic and possess a flow limit that increases with concentration.
There exists a possibility of injecting poly-acrylamide solutions in water or also salt water over the entire face of the deposit. Thereby, the very large molecules in the water-bearing pore area should be adsorbed on the matrix, the pores become narrower as a result and thus they impede the flow of water, while the oil-bearing pore area is little affected. Unfortunately, it has not been possible to verify this effect either in tests or in practice.
A modification of this method is represented by the fact of cross-linking polyacrylamide solutions in the deposits and thus obtain immobile gels. Either a solution of non-hydrolyzed polyacrylamides suffers the admixture of a cross-linking agent (e.g. aluminum salt), or solutions of partly hydrolyzed polyacrylamides, the pH value of which is adjusted to 3-4 to produce a minimum viscosity, are alternately injected with solutions of the cross-linking agent.
-2-~la6l6z This method is extremely costly and has not proved effective with sandstone deposits. F'or example, in field treatment, it has bee~ ascertained that out of six wells treated only in one was a partial success recorded, which possibly could also be attributed to the bore hole clearance effected before treatment. In laboratory tests it could be demon-strated that the intended gel formation, or the adherence to sandstone, does not take place, so that the flow conditions in existence before the treatment are affected only for a short time by the treatment.
SUMMARY OF THE INVENTION
This invention relates to a process for reducing the influx of water from a subterranean petroleum-bearing porous matrix formation into a producing well, that has undergone a preliminary pumping of clean oil, comprising the injection into the said porous matrix formation via said producing well of a slug of an emulsion of gel globules of a polyacrylamide polymer in mineral oil, said globules having a maximum diameter of less than half of the pore width of said porous matrix, wherein said slug is injected in amounts sufficient to penetrate from 3 to 10 meters into said formation adjacent said producing well.
BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1. Top view of plexiglass test model.
Figure 2. View of steel pipe test model.
DETAILED DESCRIPTION OF THE INVENTION
The object of the present invention is to produce a process whereby the flow of water into production wells can be reduced for a long period, without impending the pro-duction of oil therefrom.

C

li~616Z

It has IlOW been found that it is possible to usepolyacrylamide liquid polymers, as available in the trade, for inhibiting the flow of water into production wells.
These polymer solutions are emulsions of highly concentrated gels of polyacrylamides in the form of little balls in mineral oil. The diameter of the balls should be 0.5 to 5.0~m. Preferred are emulsions of the gel globules which have a diameter smaller than 2 ~ m. The concentration of the emulsion in dry polyacrylamide is 25 to 35%, in oil 33 to 50%, and in water 25 to 35%. It is possible to dilute as desired these liquid polymers with mineral oil, e.g. diesel fuel, without the gel becoming modified; they simply sediment.

~.

-3a-, If the emulsion in water or salt water is introduced while stirring, the gel particles are cross-linked with water, they swell, they partly agglomerate and after a relatively long time, a few hours, or several days, depending upon the temperature and the intensity of stirring, they go into solution. As polyacrylamide solutions, because of their high molecular weight - several million - already in a small concentration, increase the viscosity of the water or salt water considerably, it is possible to dilute the liquid polymers to a very high multiple with mineral oil for effective water inhibiting processes. Thus, the vis¢osity of water of small hardness (3.5 dh) is already considerably increased by 0.25 kg partly hydrolyzed polyacrylamide per m3, particularly in the case of a small speed gradient;
highly-saline deposit water requires at any rate about 2 kg polyacrylamide per cubic meter, the hydrolysis degree having little effect in this connection. These polyacrylamide emulsions thus remain unaltered on mixing with oil, i.e. with a low degree of viscosity, but they become highly vlscous to gel-like on mixing with water. Their colloid fine particles are injectable into the pore spaces, as their diameter is smaller than the pore diameters in the deposit. On cross-linking with water or salt water they swell and already in small concentration they considerably increase the viscosity of the water.
The concentration of the solution of liquid polymer to be injected into a particular deposit, as well as the appropriate volume of the solution to be injected will be determined empirically by means of tests on deposit cores or comparable sand packs with deposit oil and water, as well as at deposit temperature.

11~'~1i2 The following characteristics must be made on the liquid polymer: the emulsion must be emulsified finely enough, the polyacrylamide being as far as possible high-molecular and preferably partly hydrolyzed, as anionic polymers are better absorbed on the matrix.
The tests described below illustrate the effective-ness of the process according to the invention.
In the first test use was made of a deposit model of plexiglass filled with sand, the top view and dimensions of which are shown in Figure 1. The thickness of the sand pack was 2 cm. The grain size of the sand was 0 to 0.15 mm, the porosity of the pack was 48%, the permeability approximately 6~m2 (Darcy), the average pore diameter approximately 4 Jum. The pack was first filled with deposit water with a salt content of 165 g/l. Thereafter the model was flooded with a mineral oil of 15 mPa.s viscosity to simulate an original deposit condition. The pore space of 1760 ml was to the extent of 1388 ml filled with oil (79%) and contained 21% connate water. For comparison, in the first instance, a floodlng test was carrled out wlth deposit water without any treatment for water shut-off. Deposit water was in~ected into well A and well M acted as a production well. (The other wells marked in Fig. 1 were used only for charging the model). Three times the volume of the entire pore volume had to be injected before the liquid produced, the wet oil, was flooded to 96%. Until then 66% of the originally available oil was produced. Thereafter, by flooding with oil, the original state was again produced.
The second flooding test was started in the same 0 way as the first, deposit water injected in A and oil or .
llC6162 oil and ~later was drawn out of M. For a water contentof the ~iet oil of 80% flooding was interrupted and the process according to the invention used. Then, the following liquids were iniected one after the other into the well M, while wells A and C lay open for outflow: 19 ml diesel fuel, 130 ml of a 6% solution of a highly viscous polyacrylamide liquid polymer in diesel fuel, 13 ml mineral oil with 15 mPa.s. The liquid polymer was partly hydrolyzed to 30%
and had a limit viscosity of about 28 cP as well as a gel particle size of < 2 ~m. In the test, from C there flowed only oil, from a rather smaller quantity consisting of 94%
salt water and 6% oil.
; The next day flooding was again undertaken as at the beginning, injection in A, production from r~. In the test, at first, 165 ml oil were produced free of water, a mixture of the injected diesel fuel and 15 mPa.s mineral oil.
Then, flooding increased relatively quickly to about 75%.
To allow more time for the swelling out of the gel particles -the test was conducted at room temperature - the packing was closed for three days. After the resumption of the flooding the water intrusion was only 20% approximately, and did not increase again till a substantial amount of oil had been obtained. Up to 96% water intrusion there were injected in the flooding phases altogether only 1.35 pore volumes of salt water and 76% of the original oil were obtained (the oil : remaining in the packing in the treatment being deducted).
The two facts, the oil production increased by some 15%
and the shortening of the life of a field, associated with the substantially smaller amount of wet oil to be clarified, mean for the field application of the process considerable profit or savings.

`

~1~616Z

A third test for the reduction of the water inflow was better suited tO the deposit conditions in that crude oil instead of mineral oil refined product was used and the operations conducted at a temperature of 58 C, corresponding to a formation temperature at a depth of about 1500 m. A
steel pipe of 3 cm diameter and 80 cm long was filled with said of the same type as in the first test. It was possible to flood and also to produce into the tube from both ends and from a hole in the middle (Fig. 2). The pore space was first of all filled with deposit water, then with crude oil (9 mPa.s at 58C) flooded over the entire length. Only one side, A after M, was flooded out with deposit water up to 99% intrusion of water. An initial state was produced in that in A deposit water (0.7 mPa.s at 58C) and in B crude oil at the same pressure were injected. The wet oil produced from M became constant at 86.7% water intrusion.
The flow rates were for oil 167 ml/h bar and for water - 1090 ml/h bar.
The treatment for the reduction of the water inflow consisted in the injection in M of 8 ml diesel fuel, 84 ml of a 6% solution of polyacrylamide liquid polymer as available in the trade in diesel fuel and 31 ml of a mineral oil (6 mPa.s at 58C). Flooding was resumed after 16 hours, injection of deposit water in A, of crude oil in B.
After almost all the injected oil quantity was flowed free from water out of M, the oil flow stabilized at 48 ml/h bar, while the water inflow increased at first, but after : a maximum of 100 ml/h bar was reached, it decreased constantly, particularly after a further interruption of flooding at 10 ml/h bar. ~ater intrusion amounted still to only 18%, :

61~iZ

the f`low rate for water was less than 1% of the original.The flow rate for oil was reduced to 29% of the original.
~or oil production the water/oil flow rates ratio is decisive.
The absolute values at adequately high initial permeability are without effect upon the daily production rates, and when conditions are favorable an increased daily oil production is even possible.
In further tests it was ascertained that already with 1% solutions of polyacrylamide liquid polymer in diesel oil substantial reductions of the water inflow are obtained.
Furthermore, instead of diesel oil it is possible to use other hydrocarbon oils for dilution to liquid polymers, such as heavy petroleum or light machine oil refined products and also crude petroleum. It is necessary that the oils should be free from water and contain no substances which would lead to the clotting of gel globules, which could be the case with many crude oils. Low-viscous oils are given preference, because, as they flow through water-bearing pore spaces, there takes place a faster thorough mixing with water, the gel particles are cross-linked more quickly and swell faster.
The viscosity of these oils should be about 2 to 10 cP.
When choosing suitable oils the suitability of the deposit oil plays a part.
For a good effectiveness of the process according to the invention various parameters are of importance. The economic optimum shall be determined empirically. A
prerequisite is that the polyacrylamide liquid polymer should be emulsified finely enough, and the largest gel globules should be about half as big, as a maximum, as the pore width of the matrix rock. Furthermore, it is important :

llC61~i~

that the ~1O~J p3ths up to entry into the matrix be free from water, ~}liS condition being achieved by the preliminary pumping of clean oil. The concentration of the liquid polymer dissolved in oil (partly hydrolyzed polyacrylamide) may be small, e.g. 1%, if the deposit contains soft water. -~
With a high salt content of the deposit water higher concen-trations are to be recommended, 5 to 10%. The volume of the emulsion solution must be selected such that it penetrates to several meters distance into the deposit formation, - 10 adjacent the producing well. Preferably the penetration into the formation should be about 3 to 10 meters. Also - the volume of the more highly viscous oil subsequently injected into the formation, which oil may also be crude oil, is to be selected appropriately such that on the one hand the liquid polymer solution mixes more intensively in the water-bearing layer with the deposit water and, on the other hand, in order to push back in the oil-bearing layer in the ' immediate vicinity of the produclng well, as a result of which the oil inflow is prevented to a lesser degree. It is preferred that the oil be in~ected in amounts such that the emulsion solution is displaced into the formation to a distance of 1 to 5 meters. In this system, the perforations present in the zone originally supplying water also remain ; open and are useful for production. Filling these perfora-tions with cement before or after treatment would therefore be detrimental.
The technical carrying out of a treatment requires no unusual or costly equipment. The underground installations or the well are not modified, and only the incorporated plunger pump only requires to be drawn. The making available _g_ .

~1~61~Z

ls requ1red of tanks with the dilution oil (diesel oil, degassed conderlsate or the like), with the more viscous oil (machine oil, crude oil), and a smaller tank for the polyacrylamide liquid polymer, also an injection pump and a metering pump, which in.jects the liquid polymer solution into the sucf ion duct of the injection pump. Both pumps should have provision for regulating and controlling flow rates, so that the desired injection rate and the concentra-tion may be adjusted.
The advantage of the present liquid polymer process lies in that the whole thickness of the deposit can be treated, independently of which part of the thickness bears water or whether the water flows in a particular area over :~ the whole thickness to the well, while the oil flows from specific parts in a continuous stream to the drill hole, which is afforded in most cases up to very high intrusion of water. As emulsions can be ma.de finely dispersed almost as desired, the size of the gel globules of the liquid polymer - insofar as the gel globules are not bigger than 0.5 to 5.0JU m - hardly causes a restrlction of applicability, as deposits with permeabilities of 0.1 ~ m2 (100 m Darcy) or over can be treated with success.
.~

. .

Claims (7)

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:
1. A process for reducing the influx of water from a subterranean petroleum-bearing porous matrix for-mation into a producing well said well having undergone a preliminary pumping of clean oil comprising the injection into said porous matrix formation via said producing well of a slug of an emulsion of gel globules of a polyacrylamide polymer in mineral oil, said globules having a maximum diameter of less than half of the pore width of said porous matrix wherein said slug is injected in amounts sufficient to penetrate from 3 to 10 meters into said formation ad-jacent said producing well.
2. A process according to Claim 1, wherein said polyacrylamide is hydrolyzed to 10 to 60%.
3. A process according to Claim 2, wherein said polyacrylamide is hydrolyzed to 20 to 35%.
4. The process of Claim 1, wherein said gel globules have a maximum diameter of from 0.5 to 5.0 µm.
5. A process according to Claim 1, wherein such gel globules consist of 25% to 30% dry polyacrylamide polymer and 50% to 75% water.
6. A process according to Claim 1, wherein said emulsion is diluted before the injection into said producing well with a low-viscosity mineral oil, so that the gel concentration in the injected emulsion is between 1.0 and 5%.
7. A process according to Claim 1, wherein a more highly viscous mineral oil is subsequently pumped into said producing well behind said emulsion in such amounts that the said emulsion solution is displaced into said formation to a further distance of 1 to 5 meters.
CA316,441A 1977-11-19 1978-11-17 Process for reducing water influx into gas or oil producing wells Expired CA1106162A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2751716 1977-11-19
DEP2751716.4 1977-11-19

Publications (1)

Publication Number Publication Date
CA1106162A true CA1106162A (en) 1981-08-04

Family

ID=6024101

Family Applications (1)

Application Number Title Priority Date Filing Date
CA316,441A Expired CA1106162A (en) 1977-11-19 1978-11-17 Process for reducing water influx into gas or oil producing wells

Country Status (3)

Country Link
CA (1) CA1106162A (en)
FR (1) FR2409374A1 (en)
GB (1) GB2008651A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01299993A (en) * 1988-05-27 1989-12-04 Toho Chem Ind Co Ltd Closing method for mud escape part
GB2325478A (en) 1997-05-24 1998-11-25 Sofitech Nv Emulsion for well and formation treatment

Also Published As

Publication number Publication date
FR2409374A1 (en) 1979-06-15
GB2008651A (en) 1979-06-06

Similar Documents

Publication Publication Date Title
US4276935A (en) Treatment of subsurface gas-bearing formations to reduce water production therefrom
US3308885A (en) Treatment of subsurface hydrocarbon fluid-bearing formations to reduce water production therefrom
US3747681A (en) Hydraulic fracturing process using polyethylene oxide based fracturing fluid
US3455390A (en) Low fluid loss well treating composition and method
US5105884A (en) Foam for improving sweep efficiency in subterranean oil-bearing formations
Clark A hydraulic process for increasing the productivity of wells
US3710865A (en) Method of fracturing subterranean formations using oil-in-water emulsions
US5604184A (en) Chemically inert resin coated proppant system for control of proppant flowback in hydraulically fractured wells
US3378074A (en) Method for fracturing subterranean formations
US8076271B2 (en) Aqueous tackifier and methods of controlling particulates
CA2422509C (en) Real-time reservoir fracturing process
US5101903A (en) Method for modifying the permeability of an underground formation
US5425421A (en) Method for sealing unwanted fractures in fluid-producing earth formations
CN113646381B (en) Reverse emulsion for hydraulic fracturing
US3126056A (en) Hydraulic fracturing of earth formations
WO2017095253A1 (en) Method of treating a well with the formation of proppant structures (variants)
US6273192B1 (en) Method for strengthening a subterranean formation
US3749174A (en) Method for selective plugging of wells
US5067564A (en) Selective placement of a permeability-reducing material to inhibit fluid communication between a near well bore interval and an underlying aquifer
US3138205A (en) Hydraulic fracturing method
USRE32114E (en) Oil recovery process
US4433727A (en) Oil recovery process
US4662447A (en) Gravel packing method and apparatus
US4580627A (en) Oil recovery process and system
US3766986A (en) Method of treating a well using a volatile hydrocarbon liquid

Legal Events

Date Code Title Description
MKEX Expiry