US2034347A - Method of treating wells - Google Patents
Method of treating wells Download PDFInfo
- Publication number
- US2034347A US2034347A US3978A US397835A US2034347A US 2034347 A US2034347 A US 2034347A US 3978 A US3978 A US 3978A US 397835 A US397835 A US 397835A US 2034347 A US2034347 A US 2034347A
- Authority
- US
- United States
- Prior art keywords
- solution
- water
- cellulose
- well
- oil
- 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 - Lifetime
Links
- 238000000034 method Methods 0.000 title description 17
- 239000000243 solution Substances 0.000 description 109
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 67
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 48
- 229920002678 cellulose Polymers 0.000 description 48
- 239000001913 cellulose Substances 0.000 description 45
- 230000015572 biosynthetic process Effects 0.000 description 37
- 238000005755 formation reaction Methods 0.000 description 37
- 239000003921 oil Substances 0.000 description 25
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 235000011121 sodium hydroxide Nutrition 0.000 description 16
- 239000012267 brine Substances 0.000 description 11
- 230000008021 deposition Effects 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000011148 porous material Substances 0.000 description 11
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 11
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 10
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 10
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 10
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 229920000297 Rayon Polymers 0.000 description 9
- 229920002301 cellulose acetate Polymers 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000012895 dilution Substances 0.000 description 8
- 238000010790 dilution Methods 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 229920001220 nitrocellulos Polymers 0.000 description 7
- 239000003129 oil well Substances 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- 238000001556 precipitation Methods 0.000 description 7
- 238000007789 sealing Methods 0.000 description 7
- 239000003643 water by type Substances 0.000 description 7
- 239000000020 Nitrocellulose Substances 0.000 description 6
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 229940079938 nitrocellulose Drugs 0.000 description 5
- 239000002966 varnish Substances 0.000 description 5
- 239000003513 alkali Substances 0.000 description 4
- 239000003518 caustics Substances 0.000 description 4
- 230000003111 delayed effect Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000002028 premature Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 230000008961 swelling Effects 0.000 description 3
- 239000002349 well water Substances 0.000 description 3
- 235000020681 well water Nutrition 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 238000005189 flocculation Methods 0.000 description 2
- 230000016615 flocculation Effects 0.000 description 2
- 239000008398 formation water Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 239000003566 sealing material Substances 0.000 description 2
- 235000002639 sodium chloride Nutrition 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- GFVUWETXLKDTIO-UHFFFAOYSA-J [C+4].[SH-].[SH-].[SH-].[SH-] Chemical compound [C+4].[SH-].[SH-].[SH-].[SH-] GFVUWETXLKDTIO-UHFFFAOYSA-J 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- QKSIFUGZHOUETI-UHFFFAOYSA-N copper;azane Chemical compound N.N.N.N.[Cu+2] QKSIFUGZHOUETI-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- -1 say 5-10 per cent Chemical compound 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/50—Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
- C09K8/504—Compositions based on water or polar solvents
- C09K8/506—Compositions based on water or polar solvents containing organic compounds
- C09K8/508—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
- C09K8/514—Compositions based on water or polar solvents containing organic compounds macromolecular compounds of natural origin, e.g. polysaccharides, cellulose
Definitions
- the pressure gradient is not so high in points remote from the well face.
- the solution used is one which precipitates on dilu tion or deposits by other ways, such as flocculation, a sealing plug or deposit in the water formation.
- Cellulose solutions, aqueous and non-aqueous are especially usefulfor our purposes.
- the solution is; forced into the well under pressure sufficient to drive it far back into the water We do this strata- Diffusion and intermingling of the solution with the water in the formation bring about the deposition desired.
- the solution is left in the formation, pressure being maintained,
- the well is first cleared of any brine or water standing therein by displacing the brine upwards with oil.
- solutions of various-kinds of organic colloids having the properties described can be used, we have found that solutions of cellulose derivatives have particularly useful properties for our purposes. Almost any soluble form of cellulose dissolved in an appropriate solvent can be employed. Certain cellulose derivatives like hydroXy-ethyl cellulose, which goes into solution in aqueous caustic alkali; solutionsof. cellulose esters like pyroxylin; viscose solutions (a modifled form of cellulose in water solution); and
- solutions comprising cellulose dissolved with the aid of copper-ammonia reagent or 'zlnc chlorid reagent are all suitable.
- a form of cellulose or modified cellulose is gradually deposited out.
- the deposit in each case is of a more or less bulky, fibrous nature and, although quite insoluble, swells with 40 water, increasing thebulk and sealing eflect.
- Viscose is'a colloidal solution of cellulose, containing a modified form of cellulose, water, carbon disulfid and caustic 5 soda. It is usually made by allowing cottodfiber to swell in caustic soda solution and treating with carbon bisulfid.
- the product which may be regarded as a sodium salt of cellulose x'anthate, can be dissolved inwater or in water -sw'ells in place by taking up more water.
- a useful solution for our purpose comprises a mixture of one part viscose with ten parts water, by weight.
- a well which penetrates both oil and water' sands is treated to plug the water sands selectively. Water standing in the well is displaced upward with dry oil.
- a batch of solution comprising ten parts by weight commercial viscose dissolved in one hundred parts by weight Water containing a little acetic acid is injected into the well under high pressure, and pressure is maintained for a day. At the end of this time pressure is released and the well allowed to flow. It is found the water flow is substantially shut oif, while oil flow is unaffected.
- Caustic soda solutions of certain other cellulose derivatives are likewise useful in the invention.
- Caustic potash may be substituted for the canstic soda in such mixtures, but caustic soda is cheaper and has certain advantages.
- caustic soda solutions frequently have but little viscosity. This is particularly true of solutions of hydroxy-ethyl cellulose; a body which is now made by various methods, including treating moist cellulose with ethylene oxid. This material can be dissolved in 5 to '7 per cent caustic soda solution to give liquids carrying about 0.5 pound per gallon of hydroxy-ethyl cellulose in solution.
- Such a solution can be used directly in the invention, but somewhat more concentrated solutions are generally more desirable.
- the solution can contain 10 per cent or more caustic soda by weight and about 0.8 pound hydroxy-ethyl cellulose per gallon of solution.-
- the resulting liquid has a viscosity only slightly greater than that of water and it can be readily pumped,
- fiocky and gelatinized clogging body is produced when the concentration of caustic soda drops to about '2 per cent or below. This precipitate The presence of salines in the well water does not deleteriously aifect the action; flocculation takes place equally eifectively with brine.
- any water standing in the well is displaced with dry oil and the treating solution is then injected directly, under high pressure, forcing the waters back into the formations before it. It is not necessary to force back the well waters with fresh water, before injection of the solution, and in fact this is generally to be avoided, asit may cause premature precipitation, or a precipitation in the oil formation where the plastic is not wanted.
- an oil well penetrating oil bearing and brine bearing strata is freedof brine and the brine inflow stopped, by pumping in dry oil under pressure.
- the described solution of hydroxy-ethyl cellulose dissolved in about 10 per cent caustic soda solution is forced into the well.
- the cellulose solu tion enters the wet formations, forcing the brine therein ahead of it without any immediate substantial dilution of the solution in a given pore.
- the high caustic soda concentration used permits the cellulose solution to be forced back a considerable distance into the water bearing strata prior to the formation of a precipitate.
- the precipitated cellulose swells, sealing the pores tightly and resisting dislodgmentl After a pause to allow flocking in the pores, the residual cellulose solution in the well may be pumped out and used elsewhere, being strengthened if it be thought desirable, by solutions of more caustic soda and more hydroxyethyl cellulose, either or both.
- cellulose solutions of this general type are useful, such as alkaline aqueous solutions of so-called oxycelluloses and hydrocelluloses.
- the oxycelluloses are products formed by the action of certain oxidizing agents on cellulose and the hydrocelluloses are obtained bythe action on cellulose of cold, concentrated mineral acids, or by boiling cellulose with acetic acid contain- ,ing about 2 per cent of sulphuric acid.
- Both oxycellulose and hydrocellulose prepared in this way can be put into solution by steeping in strong caustic soda solution (approximately 10 normal) and diluting the mixture until the solution is about 2 normal with respect to caustic soda.
- solubility is a maximum in 2N caustic soda I solution.
- Another modification which is particularly use- 111 in certain relations makes use of certain cellulose derivatives or esters dissolved in an appropriate organic solvent, usually one miscible with water to a greater or less extent.
- an appropriate organic solvent usually one miscible with water to a greater or less extent.
- a solution of acellulose ester such as cellulose nitrate or acetate in an' organic solvent, usually one of the oxygenated organic type including alcohols, ketones, etc.
- the solution forces the local water ahead of it in the formation.
- the solution on dilution with water, deposits the cellulose ester as a bulky solid body, swelling with the absorption of more water as the solvent disappears.
- Such a solution in a channel is diluted by diffusion of water into it from adjacent wet rock or earth.
- sidual solution is pumped out of the'well the plugging of the pores is permanent.
- the commercial varnishes also contain high boiling plasticizers which have no particular effect either way in the present invention and a minor proportion of a nonsolvent" (benzol or gasoline) used to make the varnish less hygroscopic; less sensitive to the ac- 7
- a nonsolvent benzol or gasoline
- These non-solvents in the commercial varnishes are not harmful for the present purposes. They are indeed of some ad-' vantage in securing the delayed action desirable in the present invention.- For the same reason, in mamng up special solutions for well plugging it is often advantageous to incorporate a little benzol, say 5-10 per cent, ora miscible gasoline with the compositions.
- any water or brine standing in the well is advanta-' geously bailed out or is displaced upwards with dry oil poured into the casing.
- the waters are forced back into the formation by means of a charge of organic liquid, usually the same solventas is used in making the treating solution; this being introduced into the wellunder high pressure. This forces back the water in the channels in the wet formation and is later itself displaced in the same way by the treating solution injected into the well; also under high pressure. This latter penetrates a considerable distance into the wet formation. The previous removal ofthe water prevents premature precipitation.
- the solvent employed- also depends on the type of cellulose derivative or ester selected.
- the solvent is usually one of the oxygen-containing organic type including alcohols, ketones, etc.
- Cellulose acetate dissolved in acetone is useful and cheap. Eight ounces of a certain commercial grade of cellulose acetate can be dissolved in 1 gallon of acetone to form a solution having a viscosity of-about 2.6 centipoises at 25C. (The viscosity of water at this'temperature is 0.9 centipoise.)
- the cellulose acetate in this case is of a low viscosity grade, approximately equivalent to that of a 0.5 second nitrocellulose. That is, 0.5 second nitrocellulose dissolved in acetone in similar proportions gives a solution of about the same viscosity.
- Cellulose acetate dissolved in acetic acid is useful particularly in a modification of the invem tion adapted for treating diflicult cases: high pressure formations and very pervious formations.
- a solution comprising 5.7 pounds cellulose acetate in pounds 99.5 per cent acetic acid requires dilution with a volume of water equal to the volume of the solution, before any deposition occurs. In ordinary treatment, this solution can be injected into the. well. immediately after displacing the standing water with oil. No previous forcing back of local water is necessary.
- the waters can be forced back into, the formation with acetic acid, and the solution then injected. This allows of the solution being forced a great distance into the formation before deposition occurs.
- the deposit is formed at remote points, where the pressure gradient is lowest; and, opportunity is given for provision of a greater quantity of sealing matter.
- cellulose ester solutions being immiscible with petroleum oils. Any of the treating solution getting into the oil formation is simply flushed out when the well is allowed to prov an oil well penetrating water sands, a batch of treating solution is made up comprising 7.55 pounds commercial cellulose acetate dissolved in 100 pounds acetone. The solution has a viscosity of about 2.6 centipoises at 25 C. It'is relatively mobile and can be readily pumped and piped with ordinary oil well equipment; Water standing in the well is displaced upwards with a charge of dry oil. The formation water is now forced back with a charge of acetone introduced under pressure.
- treating solutions can be of high concentration, containing a relatively high pro-.
- dissolved cellulose it is generally better to employ the-less concentrated solutions. They are easier to pipe; pump and handle and are not so sensitive to precipitation on contact with water. They do not precipitate prematurely.
- the viscosity of these suitable solutions can range from the minimum possible to the maximum which still allows the solution to be pumped and piped.
- the method of treating oil wells which penetrate oil and water formations for stopping water inflow to the well without hindering oil flow which comprises introducing into the well a solution of a cellulose material adapted to deposit out as an insoluble precipitate when diluted with water, maintaining pressure on such material in the well while allowing water in the well to contact with such material to cause deposition, releasing the pressure and allowing the well to flow.
- the solution comprises a cellulose material dissolved in .an organic solution of the oxygen-containing type. 6. The process of claim 1 wherein the solution comprises a cellulose material in alkaline solution.
- the solution comprises hydroxy-ethyl cellulose and caustic soda, the caustic soda. being in proportion at least 10 per cent by weight of the solution.
- the solution comprises a cellulose derivative dissolved in an organic solvent in proportions such as to secure a viscosity of about 15 centipoises at 25 C., the cellulose precipitating on removal of the solvent as a voluminous hydrated deposit, swelling with
Description
ensures a!- 11, 19st 2,034,341 mop or TREATlNG s Albert G. Loomis, Mount Lebanon Township, Al-
legheny "County, and Abraham .l. Teplitz and Henry A. Ambrose, Pittsburgh, Pa., assignors .to Gulf Research & Development Corporation,
Wilmington, Del., a corporation of Delaware No Drawing.
Application January 29, .1935,
Serial No. 3,978 1i Claims. (Cl. 166-221) Oil wells often pass through a variety of ground formations including oil bearing and water bearing formations, these often being closely adj acent. It is adesideratum to shut off the inflow of connate water or brine from wet formations and it is, of course, essential to avoid any stoppingofii of inflow of oil from the oil containing formations. No good way of effecting such selective stopping 01f has been known in the art. It is common practice to stop off all infiow to a well by means of mud or concrete plastering the walls. A
frequent expedient is to inject a concrete mixture setting to a solid mass andlater drill through the solid body thus formed. This expedient can be used for shutting off water occurring in the well bottom but it is not adapted for shutting off water occurring elsewhere than in the well bot- 3 tom. In certain cases water formations lying above the oil formation can be shut off by steel casings. But this method is not discriminatory, is not effective in some situations and is always costly.
In an oil well there is a sharp pressure gradient at the well face and it is diflicult to keep sealing materials in place at this point; the pressure hehind tends to break the seal and clear the pores.'
The farther back in the formation the sealing material can be used in plugging pores, the better; the less is the difficulty in keeping it in place. The pressure gradient is not so high in points remote from the well face.
We have found a way to eifect selective stopping off of water bearing strata, sealing them at points remote from the well face. with the aid of certain organic colloidal'solutions and suspensions of one kind of another. The solution used is one which precipitates on dilu tion or deposits by other ways, such as flocculation, a sealing plug or deposit in the water formation. Cellulose solutions, aqueous and non-aqueous, are especially usefulfor our purposes. The solution is; forced into the well under pressure sufficient to drive it far back into the water We do this strata- Diffusion and intermingling of the solution with the water in the formation bring about the deposition desired. The solution is left in the formation, pressure being maintained,
long
enoughfor' the deposition to take place. Ordinarily, deposition or precipitation does not take placeimmediately, but in the course of some minutes or hours. This delayed action insures against premature deposition.
In some cases, before injection of the treating 10 solution, the well is first cleared of any brine or water standing therein by displacing the brine upwards with oil.
Little penetration occurs in the oil-containing strata, particularly in the case of aqueous solutions or suspensions; these being incompatible with oil. Moreover, the delayed actions utilized are generally .of such character as not to occur in the absence of water or salines.
While solutions of various-kinds of organic colloids having the properties described can be used, we have found that solutions of cellulose derivatives have particularly useful properties for our purposes. Almost any soluble form of cellulose dissolved in an appropriate solvent can be employed. Certain cellulose derivatives like hydroXy-ethyl cellulose, which goes into solution in aqueous caustic alkali; solutionsof. cellulose esters like pyroxylin; viscose solutions (a modifled form of cellulose in water solution); and
solutions comprising cellulose dissolved with the aid of copper-ammonia reagent or 'zlnc chlorid reagent are all suitable. In each case, on allowing intermingling of the more or less concentrat ed cellulose solution with water or' brine, ordinarily the connate waters in the formations adjacent the well, a form of cellulose or modified cellulose is gradually deposited out. The deposit in each case is of a more or less bulky, fibrous nature and, although quite insoluble, swells with 40 water, increasing thebulk and sealing eflect.
Aqueous solutions of cellulose derivatives, and
solutions of cellulose materials in organic solvents, are particularly useful for our purposes.
There are certain forms of cellulose derivatives 5 which can be put'into solution in water, sometimes with the aid of alkali or acid. One such solution comprises viscose. Viscose is'a colloidal solution of cellulose, containing a modified form of cellulose, water, carbon disulfid and caustic 5 soda. It is usually made by allowing cottodfiber to swell in caustic soda solution and treating with carbon bisulfid. The product, which may be regarded as a sodium salt of cellulose x'anthate, can be dissolved inwater or in water -sw'ells in place by taking up more water.
slightly acidified with acetic acid, to form a solution useful for the present purposes. A useful solution for our purpose comprises a mixture of one part viscose with ten parts water, by weight.
' For complete precipitation to occur, a day or so may be necessary. The action is accelerated by warmth, and takes place fairly rapidly in the conditions encountered in deep wells.
In an example of a specific embodiment of the invention utilizing a viscose. solution, a well which penetrates both oil and water' sands is treated to plug the water sands selectively. Water standing in the well is displaced upward with dry oil. A batch of solution comprising ten parts by weight commercial viscose dissolved in one hundred parts by weight Water containing a little acetic acid is injected into the well under high pressure, and pressure is maintained for a day. At the end of this time pressure is released and the well allowed to flow. It is found the water flow is substantially shut oif, while oil flow is unaffected.
Caustic soda solutions of certain other cellulose derivatives are likewise useful in the invention. Caustic potash may be substituted for the canstic soda in such mixtures, but caustic soda is cheaper and has certain advantages. While many solutions of cellulose derivativesare gummy and hard to handle, caustic soda solutions frequently have but little viscosity. This is particularly true of solutions of hydroxy-ethyl cellulose; a body which is now made by various methods, including treating moist cellulose with ethylene oxid. This material can be dissolved in 5 to '7 per cent caustic soda solution to give liquids carrying about 0.5 pound per gallon of hydroxy-ethyl cellulose in solution. Such a solution can be used directly in the invention, but somewhat more concentrated solutions are generally more desirable. For example, the solution can contain 10 per cent or more caustic soda by weight and about 0.8 pound hydroxy-ethyl cellulose per gallon of solution.- The resulting liquid has a viscosity only slightly greater than that of water and it can be readily pumped,
piped and handled. On dilution with water, a
fiocky and gelatinized clogging body is produced when the concentration of caustic soda drops to about '2 per cent or below. This precipitate The presence of salines in the well water does not deleteriously aifect the action; flocculation takes place equally eifectively with brine.
In practice, any water standing in the well is displaced with dry oil and the treating solution is then injected directly, under high pressure, forcing the waters back into the formations before it. It is not necessary to force back the well waters with fresh water, before injection of the solution, and in fact this is generally to be avoided, asit may cause premature precipitation, or a precipitation in the oil formation where the plastic is not wanted.
In an example of a particular embodiment of the present invention, utilizing alkaline aqueous hydroxy-ethyl cellulose, an oil well penetrating oil bearing and brine bearing strata is freedof brine and the brine inflow stopped, by pumping in dry oil under pressure. At this time, into the well is forced the described solution of hydroxy-ethyl cellulose dissolved in about 10 per cent caustic soda solution. The cellulose solu tion enters the wet formations, forcing the brine therein ahead of it without any immediate substantial dilution of the solution in a given pore. The high caustic soda concentration used permits the cellulose solution to be forced back a considerable distance into the water bearing strata prior to the formation of a precipitate. On interrupting the supply of cellulose solution without releasing the pressure, dilution of the liquid occurs by undisplaced brine retained adjacent the pores. When this dilution, which is largely a diffusion phenomenon, reduces the caustic concentration to 2 per cent or less, a voluminous deposit occurs in the pores and swells therein, effectively plugging them. The further back in the formation this plugging occurs, the better, since the pressure differential which the plug must resist, progressively diminishes in going backward. As stated, the precipitated cellulose swells, sealing the pores tightly and resisting dislodgmentl After a pause to allow flocking in the pores, the residual cellulose solution in the well may be pumped out and used elsewhere, being strengthened if it be thought desirable, by solutions of more caustic soda and more hydroxyethyl cellulose, either or both.
Other cellulose solutions of this general type are useful, such as alkaline aqueous solutions of so-called oxycelluloses and hydrocelluloses. The oxycelluloses are products formed by the action of certain oxidizing agents on cellulose and the hydrocelluloses are obtained bythe action on cellulose of cold, concentrated mineral acids, or by boiling cellulose with acetic acid contain- ,ing about 2 per cent of sulphuric acid. Both oxycellulose and hydrocellulose prepared in this way can be put into solution by steeping in strong caustic soda solution (approximately 10 normal) and diluting the mixture until the solution is about 2 normal with respect to caustic soda. In this way, as much as 36 per cent of oxycellulose or 33 per cent of hydrocellulose can be held in solution in the dilutedcaustic solution, at 15 C. Upon further diluting these solutions with water the solubilities decrease sharply. The solubilities also decrease sharply if the alkali concentration is increased or decreased. In other words, the solubility is a maximum in 2N caustic soda I solution.
Another modification which is particularly use- 111 in certain relations makes use of certain cellulose derivatives or esters dissolved in an appropriate organic solvent, usually one miscible with water to a greater or less extent. Using this modification, there is injected into the well and the water bearing channels .adjacent the bore, a solution of acellulose ester such as cellulose nitrate or acetate in an' organic solvent, usually one of the oxygenated organic type including alcohols, ketones, etc. The solution forces the local water ahead of it in the formation. The solution, on dilution with water, deposits the cellulose ester as a bulky solid body, swelling with the absorption of more water as the solvent disappears. Such a solution in a channel is diluted by diffusion of water into it from adjacent wet rock or earth. When the re-,
sidual solution is pumped out of the'well the plugging of the pores is permanent.
- vents miscible with water, alcohol or acetone betion --of moisture.
" cipitable. Deposition takes place in a zone far back in the formation remote from the well face,
mg quite generally used. The commercial varnishes also contain high boiling plasticizers which have no particular effect either way in the present invention and a minor proportion of a nonsolvent" (benzol or gasoline) used to make the varnish less hygroscopic; less sensitive to the ac- 7 These non-solvents in the commercial varnishes are not harmful for the present purposes. They are indeed of some ad-' vantage in securing the delayed action desirable in the present invention.- For the same reason, in mamng up special solutions for well plugging it is often advantageous to incorporate a little benzol, say 5-10 per cent, ora miscible gasoline with the compositions.
Before injecting the treating solution, any water or brine standing in the well is advanta-' geously bailed out or is displaced upwards with dry oil poured into the casing. Then, in some embodiments, the waters are forced back into the formation by means of a charge of organic liquid, usually the same solventas is used in making the treating solution; this being introduced into the wellunder high pressure. This forces back the water in the channels in the wet formation and is later itself displaced in the same way by the treating solution injected into the well; also under high pressure. This latter penetrates a considerable distance into the wet formation. The previous removal ofthe water prevents premature precipitation. On ceasing pumping the formation waters gradually mix with and dilute the solution and the cellulosic substance is deposited as a bulky, hydrated, swelling prewhere it is most eifective in shutting oif the water. Completely water-miscible solvents like ace- 'tone and ethyl alcohol are satisfactory, while if it be desired to delay deposition as much as possible, less miscible solvents, such as some of the higher alcohols including, amyl alcohol can be used. These higher alcohols are often components of commercial varnishes. Some of the high boiling solvents used in vamishes, such as'glycol diethyl ether behave in the same. way as the higher alcohols; they are miscible with water but much more slowly than ethyl alcohol or acetone.
The solvent employed-also depends on the type of cellulose derivative or ester selected. The solventis usually one of the oxygen-containing organic type including alcohols, ketones, etc.
Cellulose acetate dissolved in acetone is useful and cheap. Eight ounces of a certain commercial grade of cellulose acetate can be dissolved in 1 gallon of acetone to form a solution having a viscosity of-about 2.6 centipoises at 25C. (The viscosity of water at this'temperature is 0.9 centipoise.) The cellulose acetate in this case is of a low viscosity grade, approximately equivalent to that of a 0.5 second nitrocellulose. That is, 0.5 second nitrocellulose dissolved in acetone in similar proportions gives a solution of about the same viscosity.
In general, solutions of relatively low viscosity,-
of the order of 15 centipoises, more or less, are more convenient to pump and pipe than those of high viscosity.
One convenient source for the cellulose solutions for the present purposes is, as stated, com-' mercial cellulose lacquers or-varnishes. These are. thinned or diluted with acetone, etc. before use, to reduce the viscosity. Many of these lacquers contain resins in addition to the cellulose acetate or cellulose nitrate; a synthetic resin' with the formation waters or brines, the solvent is slowly diluted and carried away, leaving the nitrocellulose deposited in the pores. The slow action permits the solution to be forced a considerable distance into the formation before substantial deposition occurs. In using this solution water standing in the well is bailed out and the waters forced back into the formation with a charge of alcohol and, ether mixture. Or because of the slow deposition action, this step can be omitted and the solution forced in directly after the displacement of standing water.
Cellulose acetate dissolved in acetic acid is useful particularly in a modification of the invem tion adapted for treating diflicult cases: high pressure formations and very pervious formations. A solution comprising 5.7 pounds cellulose acetate in pounds 99.5 per cent acetic acid requires dilution with a volume of water equal to the volume of the solution, before any deposition occurs. In ordinary treatment, this solution can be injected into the. well. immediately after displacing the standing water with oil. No previous forcing back of local water is necessary. In treating high pressure formations or very pervious formations, the waters can be forced back into, the formation with acetic acid, and the solution then injected. This allows of the solution being forced a great distance into the formation before deposition occurs. The deposit is formed at remote points, where the pressure gradient is lowest; and, opportunity is given for provision of a greater quantity of sealing matter.
In all the cases described there is no tendency for-cellulose to, be deposited in the oil formation,
' most of these cellulose ester solutions being immiscible with petroleum oils. Any of the treating solution getting into the oil formation is simply flushed out when the well is allowed to prov an oil well penetrating water sands, a batch of treating solution is made up comprising 7.55 pounds commercial cellulose acetate dissolved in 100 pounds acetone. The solution has a viscosity of about 2.6 centipoises at 25 C. It'is relatively mobile and can be readily pumped and piped with ordinary oil well equipment; Water standing in the well is displaced upwards with a charge of dry oil. The formation water is now forced back with a charge of acetone introduced under pressure.
into the formation. Pressure is maintained for The solution is then injected underhigh pressure sufllcient to force the solution, with the acetone ahead of it, a considerable distance I of the invention applied to plugging water sands adjacent an oil well, a batch of treating solution'is made up comprising 5 pounds nitrocellulose (tetranitrated cotton) dissolved in a batch of solvent consisting of 50 pounds per cent ethyl alcohol" and 50 pounds ether. The solution has a viscosity of about 2.0 centipoises at 25 C. Water standing in the well is displaced upwards with dry oil. The characteristics of this solution are such that precipitation is delayed. Hence it is not necessary to force back the formation water: though this can be done if especially far-reaching sealing is required. In this example, the forcing back step is omitted and the solution is forced in after the displacement step. After awhile pressure is released. It is found that the water flow is practically completely cut oif.
In a third examples. well producing water as well as oil from adjacent strata is treated to shut oh the water. A batch of pounds commersure. On release of pressure it is found that the water flow is materially reduced or completely shut oiT. The treatment can be repeated if necessary.
While the treating solutions can be of high concentration, containing a relatively high pro-.
portion of dissolved cellulose, it is generally better to employ the-less concentrated solutions. They are easier to pipe; pump and handle and are not so sensitive to precipitation on contact with water. They do not precipitate prematurely. The viscosity of these suitable solutions can range from the minimum possible to the maximum which still allows the solution to be pumped and piped.
When a well is treated with such solutions in the manner described, on dilution of the solution in the pores of the water formation a hydrated cellulosic body is precipitated as a gelatinous deposit which swells on contact with water and plugs the pores and fissures tightly. .In all cases, the cellulosic deposit produced in the water formatio'n'is highly insoluble'in water and'hence forms a permanent plug. These cellulose precipitates have a high sealing efliciency; that is to say, the hull: of the precipitate is large for a given weight of cellulose solution.
The solutions described have no corrosive efi'ect on metal parts in the pump and the well and aosaa rz no special precautions need be taken. Ordinary equipment can be used.
What we claim is:-
1. The method of treating oil wells which penetrate oil and water formations for stopping water inflow to the well without hindering oil flow, which comprises introducing into the well a solution of a cellulose material adapted to deposit out as an insoluble precipitate when diluted with water, maintaining pressure on such material in the well while allowing water in the well to contact with such material to cause deposition, releasing the pressure and allowing the well to flow.
2. The process of claim 1 wherein water standing in the well is displaced therefrom with oil forced into the well under pressure before injection of the solution. of cellulose material.
3. The process of claim 1 wherein the solution used is a. cellulose material in aqueous solution.
4. The process of claim 1 wherein the solution comprises a cellulose material in an organic solvent.
5. The process of claim 1 wherein the solution comprises a cellulose material dissolved in .an organic solution of the oxygen-containing type. 6. The process of claim 1 wherein the solution comprises a cellulose material in alkaline solution.
'7. The process of claim 1 wherein the solution used is an aqueous solution of viscose.
8. The process of claim 1 wherein the solution used comprises viscose in water solution in the proportion of about one part viscose and ten parts water by weight.
9. The process of claim 1 wherein the solution comprises hydroxy-ethyl cellulose and caustic alkali.
10. The process of claim 1 wherein the solution comprises hydroxy-ethyl cellulose and caustic soda.
11. The process of claim 1 wherein the solution comprises hydroxy-ethyl cellulose and caustic soda, the caustic soda. being in proportion at least 10 per cent by weight of the solution.
12. The process of claim 1 wherein the solution comprises a cellulose material in an organic solvent and the well waters are forced back into formation with a charge of organic solvent before the cellulose solution is injected.
13. The process of claim 1 wherein the solution comprises cellulose acetate in acetone.
14. The process of claim 1 wherein the solution comprises a cellulose derivative dissolved in an organic solvent in proportions such as to secure a viscosity of about 15 centipoises at 25 C., the cellulose precipitating on removal of the solvent as a voluminous hydrated deposit, swelling with
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3978A US2034347A (en) | 1935-01-29 | 1935-01-29 | Method of treating wells |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US3978A US2034347A (en) | 1935-01-29 | 1935-01-29 | Method of treating wells |
Publications (1)
Publication Number | Publication Date |
---|---|
US2034347A true US2034347A (en) | 1936-03-17 |
Family
ID=21708506
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US3978A Expired - Lifetime US2034347A (en) | 1935-01-29 | 1935-01-29 | Method of treating wells |
Country Status (1)
Country | Link |
---|---|
US (1) | US2034347A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2670048A (en) * | 1949-10-20 | 1954-02-23 | Stanolind Oil & Gas Co | Method of sealing porous formations |
US2747671A (en) * | 1951-10-05 | 1956-05-29 | Union Oil Co | Treatment of oil-bearing formations |
US2779416A (en) * | 1952-12-05 | 1957-01-29 | Stanolind Oil & Gas Co | Treating formations with solid forming liquids |
US2779415A (en) * | 1953-02-26 | 1957-01-29 | Stanolind Oil & Gas Co | Plugging formations with hot solutions |
US3103974A (en) * | 1960-03-18 | 1963-09-17 | Continental Oil Co | Method of selectively plugging formations |
US3378070A (en) * | 1965-09-03 | 1968-04-16 | Halliburton Co | Hydroxyethyl cellulose complex and method of plugging underground formations therewith |
US4418755A (en) * | 1979-02-14 | 1983-12-06 | Conoco Inc. | Methods of inhibiting the flow of water in subterranean formations |
FR2632351A1 (en) * | 1988-06-03 | 1989-12-08 | Elf Aquitaine | LIQUID COMPOSITION FOR THE PRODUCTION OF A GEL AND METHOD OF PLACING SUCH A GEL IN A WELL |
US5076361A (en) * | 1990-09-07 | 1991-12-31 | Texaco Inc. | Gel method for decreasing permeability around a wellbore |
US10774611B1 (en) | 2019-09-23 | 2020-09-15 | Saudi Arabian Oil Company | Method and system for microannulus sealing by galvanic deposition |
-
1935
- 1935-01-29 US US3978A patent/US2034347A/en not_active Expired - Lifetime
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2670048A (en) * | 1949-10-20 | 1954-02-23 | Stanolind Oil & Gas Co | Method of sealing porous formations |
US2747671A (en) * | 1951-10-05 | 1956-05-29 | Union Oil Co | Treatment of oil-bearing formations |
US2779416A (en) * | 1952-12-05 | 1957-01-29 | Stanolind Oil & Gas Co | Treating formations with solid forming liquids |
US2779415A (en) * | 1953-02-26 | 1957-01-29 | Stanolind Oil & Gas Co | Plugging formations with hot solutions |
US3103974A (en) * | 1960-03-18 | 1963-09-17 | Continental Oil Co | Method of selectively plugging formations |
US3378070A (en) * | 1965-09-03 | 1968-04-16 | Halliburton Co | Hydroxyethyl cellulose complex and method of plugging underground formations therewith |
US4418755A (en) * | 1979-02-14 | 1983-12-06 | Conoco Inc. | Methods of inhibiting the flow of water in subterranean formations |
FR2632351A1 (en) * | 1988-06-03 | 1989-12-08 | Elf Aquitaine | LIQUID COMPOSITION FOR THE PRODUCTION OF A GEL AND METHOD OF PLACING SUCH A GEL IN A WELL |
WO1989012157A1 (en) * | 1988-06-03 | 1989-12-14 | Societe Nationale Elf Aquitaine (Production) | Liquid composition for production of a gel, and process for inserting such gel in a well |
US5076361A (en) * | 1990-09-07 | 1991-12-31 | Texaco Inc. | Gel method for decreasing permeability around a wellbore |
US10774611B1 (en) | 2019-09-23 | 2020-09-15 | Saudi Arabian Oil Company | Method and system for microannulus sealing by galvanic deposition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3202214A (en) | Preparation and use of sodium silicate gels | |
US4553601A (en) | Method for fracturing subterranean formations | |
US2596137A (en) | Removing deposits from wells | |
US3556221A (en) | Well stimulation process | |
US2059459A (en) | Method of treating wells with acids | |
US4144179A (en) | Composition for treating low temperature subterranean well formations | |
US4265673A (en) | Polymer solutions for use in oil recovery containing a complexing agent for multivalentions | |
EP0007013B1 (en) | Gelled compositions and process for treating subterranean formations | |
RU2287549C2 (en) | Stable liquid suspension compositions and the method of their production and application | |
US2034347A (en) | Method of treating wells | |
US3881552A (en) | Shutting off water in gas wells | |
US3475334A (en) | Hydraulic fracturing | |
US2667224A (en) | Well completion process | |
US4265311A (en) | Methods of water flooding and fracturing using clean, non-damaging fracturing fluids | |
BRPI0806243B1 (en) | METHOD FOR STIMULATING A PORTION OF AN UNDERGROUND FORMATION | |
US4068720A (en) | Method for acidizing subterranean formations | |
US2778427A (en) | Acidizing wells | |
US2294078A (en) | Method of treating wells | |
US5669446A (en) | Methods for breaking viscosified fluids | |
US3696035A (en) | Well treatments with thickened aqueous alcohol mixtures | |
US2896717A (en) | Avoiding increased water production in fracturing operations | |
US4169797A (en) | Composition for acidizing subterranean formations | |
US3668122A (en) | Drilling fluid preparation | |
US2687375A (en) | Drilling fluids | |
US2825409A (en) | Hydraulic fracturing of formations |