US2799342A - Process for treating oil well formations - Google Patents
Process for treating oil well formations Download PDFInfo
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- US2799342A US2799342A US446973A US44697354A US2799342A US 2799342 A US2799342 A US 2799342A US 446973 A US446973 A US 446973A US 44697354 A US44697354 A US 44697354A US 2799342 A US2799342 A US 2799342A
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- formation
- well
- dispersion
- water
- carrier
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- 230000015572 biosynthetic process Effects 0.000 title claims description 94
- 238000000034 method Methods 0.000 title claims description 18
- 239000003129 oil well Substances 0.000 title claims description 16
- 238000005755 formation reaction Methods 0.000 title description 92
- 230000008569 process Effects 0.000 title description 10
- 239000006185 dispersion Substances 0.000 claims description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- 229910052783 alkali metal Inorganic materials 0.000 claims description 31
- 150000001340 alkali metals Chemical class 0.000 claims description 31
- 239000002415 cerumenolytic agent Substances 0.000 claims description 23
- 239000007788 liquid Substances 0.000 claims description 22
- 239000001993 wax Substances 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 13
- 239000007795 chemical reaction product Substances 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- 239000000047 product Substances 0.000 claims description 8
- 150000002739 metals Chemical class 0.000 claims description 3
- 239000011734 sodium Substances 0.000 description 21
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 20
- 229910052708 sodium Inorganic materials 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 18
- 239000003921 oil Substances 0.000 description 13
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 11
- 239000002245 particle Substances 0.000 description 9
- 229910045601 alloy Inorganic materials 0.000 description 8
- 239000000956 alloy Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000003208 petroleum Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910000573 alkali metal alloy Inorganic materials 0.000 description 3
- 230000002939 deleterious effect Effects 0.000 description 3
- 239000008398 formation water Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 230000035508 accumulation Effects 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910000799 K alloy Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229910000528 Na alloy Inorganic materials 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- -1 potassium metals Chemical class 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002250 progressing effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000003643 water by type 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
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/592—Compositions used in combination with generated heat, e.g. by steam injection
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
- E21B43/24—Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection
Definitions
- the present invention relates to a process for treating oil wells by heating a subterranean oil-bearing formation pierced by a bore hole to remove from portions of the formation adjacent the bore hole deposits or accumulations of substances which interfere with the production of petroleum from it. More particularly, this invention relates to a process for introducing into and about the formation an alkali metal which has been conditioned to spread over the exposed areas and to penetrate within the pore spaces and interstices of the formation so that the heat liberated upon reaction of the alkali metal with States Patent O formation water, or water introduced into the formation,
- the reaction would take place in a localized portion of the bore hole, and the heat generated would, in effect, be concentrated primarily in the immediate vicinity of the sodium metal mass.
- the heat would be diffused from this locus along the well bore 'and over the exposed face of the formation by the agitation-of the water and reaction products generated by the liberation of gases resulting from the reaction, as well as by heat conduction through theelements of the formation.
- .It is an object of this invention to provide a novel method for treating a subterranean formation to free it of waxy deposits which have a deleterious effect on the production of oil from it.
- Another object of the present invention is to treat a subterranean formation with an alkali metal or an alloy of alkali metals which has been conditioned before introducing it into the bore hole to place it in a form that will enable it to be spread over the exposed face of the formation and be forced into the interstices and pore spaces of the formation for an appreciable depth beyond the exposed face so that the exothermal effects of the reaction of the metal with water will be pronounced both in area and in volume.
- a dispersion of sodium metal is made in a carrier which is inert to it.
- the carrier is a wax solvent and may be, for example, a crude oil, a highly aromatic petroleum fraction, or a refined petroleum product.
- 802 extracts of diesel fuel and S02 extracts of kerosene have been found to be especially effective as solvents of waxes found in oil wells and are suitable for the purpose of this invention.
- the sodium dispersion may be made by violently mixing the metal into the carrier by a mechanical agitator until the sodium is reduced to particle sizes which will remain dispersed.
- Dispersing aids or stabilizers such as long-chain fatty acids, silicone oil or other suitable surface-active agents, may be added and the carrier and metal may be heated to aid the formation of the dispersion. Dispersing aids may be selected which also will affect the rate of reaction of the sodium with water, to control the rate at which heat is liberated by the reaction.
- an alloy of sodium and potassium metals may be used instead of sodium metal.
- the proportions of metals in the alloy may be selected so that the alloy is a liquid at ordinary temperatures and the dispersion will be that of the liquid alloy in the liquid carrier. Under these circumstances, there is obviously no criticality of particle size of the liquid alloy for the best effect on the formation.
- Lithium, potassium, rubidium and cesium also may be used separately or in combination as the reactive agent.
- the dispersion of alkali metal in its inert wax-solvent carrier may be introduced into the bore hole by one of several means. Care must be taken to remove all traces of water from the conduits through which the alkali metal dis persion is to be introduced, including the well tubing or casing down to the location of the oil-bearing formation. If, for example, the dispersion is to be introduced into the well through tubing, a slug of the water-free carrier for the dispersion is introduced into the tubing prior to plac- Patented July 16, 1957.
- the slug of carrier is forced down to the location of the formation to clear all water from the path to be taken by the dispersion.
- a quantity of alkali metal dispersion is then placed in the tubing, followed by another slug of the carrier alone. If it is necessary to do so, the final slug of carrier is placed under pressure to force the quantity of sodium dispersion down to the elevation of the formation. Sufiicient pressure is placed on the quantity of dispersion to cause it to migrate into the formation a predetermined distance. cases, the hydrostatic head of the products in the tube may be sufiicient for this purpose.
- the alkali metal distributes itself over the exposed face of and into the formation, it will contact the connate water therein and react with it to produce heat.
- the initial quantities of alkali metal will react with the water nearest the exposed face of the formation, causing that portion of the formation to be heated first.
- Subsequent particles of alkali metal migrating through the heated zone may become melted before they reach additional water with which to react.
- the melting of the alkali metal will aid it in progressing into the formation.
- the process of heating the formation in volume will continue until all of the alkali metal or water is used up. When it is desired to produce more heat than the available water in the formation will permit, additional water may be added from the surface, as required.
- Another way of introducing the dispersion into the well is by the use of a proportioning pump.
- a liquid carrier is continuously pumped into the Well and predetermined proportions of a concentrated dispersion automatically are added to it from an appropriate tank to give the desired proportion of alkali metal at the location of the formation.
- the alkali metal dispersion or a liquid alloy of alkali metals may be introduced into the bore hole in a sealed container which can be transported down to the elevation of the subterranean formation to be treated and then ruptured to release the reactive material.
- care must be taken to make sure the bore hole is substantially free from water at the location of the formation so that the reactive material will not all react in the bore hole before it can be forced into the formation.
- the well is shut-in for a time to insure reaction of the alkali metal with formation waters and the proper distribution of heat throughout the formation.
- the well may be shut-in from 1 to 4 hours to produce the desired result. While the formation and the reaction products are still warm, the well is placed on production, and the Waxes dissolved in the carrier, as well as the reaction products of the alkali metal with the formation water, will be produced out of the well to free the formation for the subsequent production of petroleum.
- Sw is the percent of pore space filled with water.
- Equation III From Equation III it can be determined that the theoretical temperature rise of the treated portion of the formation when a dispersion of one pound of sodium metal per gallon of dispersion is used will be F. maximum.
- Equation IV From Equation IV, it can be determined that the temperature rise resulting from using enough sodium for quantitative reaction with the water present will be 340 F. maximum.
- heating the formation in the manner set forth herein will have several beneficial effects in freeing it from deleterious waxy deposits.
- the heat of reaction of the alkali metal with the formation Water will, in itself, cause melting of some such deposits and the subsequent freeing of the formation.
- Just as important as this effect, however, is that created by raising the temperature of the wax solvent which is a carrier for the dispersed reactive metal. As the temperature of the solvent is raised, it becomes increasingly more effective to dissolve the waxes from the formation and thereby free it for production of oil.
- the dispersion including both the wax solvent and the reactive agent, has been caused to migrate into the formation in depth, there will take place more than a heating and cleaning of merely the exposed surface of the formation, but the effect of heat and solvent will reach beyond the exposed surface to remove the waxes that have been deposited in the pore spaces and interstices at some distance from the face.
- the method of treating an oil well which comprises introducing into said well a dispersion of alkali metals in a liquid wax solvent carrier which is inert to said metals, placing said dispersion under pressure to force a portion of said alkali metals and said liquid wax solvent carrier into an oil-bearing formation to allow said alkali metal to react with the water contained within said formation to raise the temperature of said wax solvent, reacting the remaining portion of said alkali metals with water in said oil well, and removing the reaction products and wax solvent carrier and dissolved waxes from said well while the temperature of said products and carrier is above the normal temperature of said well.
- a method for treating an oil well which comprises introducing a liquid alloy consisting essentially of sodium metal and potassium metal into said oil well, placing said liquid alloy under pressure to force said alloy into an oilbearing formation, to allow said alloy to react with water within said formation, and removing the products of reaction from said oil well.
- a method of treating an oil-bearing formation penetrated by a well bore to free said formation of waxy deposits and water which comprises removing substantially all the water from the portion of said well bore adjacent the formation to be treated, introducing into said substantially water-free portion of said well bore an aromatic wax solvent inert to alkali metal and containing dispersed therein alkali metalparticulated into sizes ranging from submicron to five micron, placing said wax solvent dispersion under pressure sufliciently greater than the pressure in said formation to force said solvent dispersion substantially into said formation to allow said alkali metal to react with the water in said formation and to raise substantially the temperature of the wax solvent within said formation, whereby the solvent power of the solvent wax is greatly increased, and removing the reaction products of alkali metal with water in the solvent and dissolved waxes from said formation and said well bore while the temperature of said products, solvent and dissolved waxes is appreciably above the normal temperature of said formation.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
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- General Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
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- Lubricants (AREA)
Description
Unite .l
PROCESS FOR TREATING OIL WELL FORMATIONS No Drawing. Application July 30, 1954, Serial No. 446,973
7 Claims. (Cl. 166-38) The present invention relates to a process for treating oil wells by heating a subterranean oil-bearing formation pierced by a bore hole to remove from portions of the formation adjacent the bore hole deposits or accumulations of substances which interfere with the production of petroleum from it. More particularly, this invention relates to a process for introducing into and about the formation an alkali metal which has been conditioned to spread over the exposed areas and to penetrate within the pore spaces and interstices of the formation so that the heat liberated upon reaction of the alkali metal with States Patent O formation water, or water introduced into the formation,
will be effective both at the exposed surface in the bore hole and in depth into the formation to accomplish the desired removal of the deleterious substances.
It is known in the art of producing petroleum from subterranean formations that various substances may precipitate or otherwise separate from the petroleum as it flows from the formation to the well bore and gradually accumulate in the portions of the formation adjacent the well bore and on the surface of the formation exposed in the Well bore. Such accumulations act to block off and continuously reduce the flow of petroleum into the well until, eventually, the production from the well is so seriously affected it may be uneconomical to continue its operation. Deposits of waxes, parafiins, bitumens, asphalts, and miscellaneous resins in well bores are familiar problems for their unfavorable effects in this regard, and various processes and devices have been employed to remove them, some with more or less success. For convenience and simplicity, the types of deposits in which we are interested, of which the foregoing are cited only by way of example, will hereafter be termed waxes, and the method of the invention will be described in relation to such waxes.
It has been proposed heretofore to introduce sodium metal and water into a well bore in a manner to cause the sodium to be reacted in the region of an oil-bearing formation with the water so that the heat produced by the reaction would melt the waxy deposits that were blocking the formation. Such proposals also contemplated a beneficial action from the hot sodium hydroxide produced by the reaction acting on the formation and also some benefit from a scrubbing action which would occur incident to the evolution of hydrogen gas to agitate the hot reaction products across the exposed face of the formation to remove deposits therefrom. In the prior art, sodium metal was used in a mass of appreciable size, such as in pellet or brick form, and was placed in the bore hole approximately at the position of the oil-bearing formation where it was reacted with water. Necessarily under such conditions, the reaction would take place in a localized portion of the bore hole, and the heat generated would, in effect, be concentrated primarily in the immediate vicinity of the sodium metal mass. The heat would be diffused from this locus along the well bore 'and over the exposed face of the formation by the agitation-of the water and reaction products generated by the liberation of gases resulting from the reaction, as well as by heat conduction through theelements of the formation.
.It is an object of this invention to provide a novel method for treating a subterranean formation to free it of waxy deposits which have a deleterious effect on the production of oil from it.
Another object of the present invention is to treat a subterranean formation with an alkali metal or an alloy of alkali metals which has been conditioned before introducing it into the bore hole to place it in a form that will enable it to be spread over the exposed face of the formation and be forced into the interstices and pore spaces of the formation for an appreciable depth beyond the exposed face so that the exothermal effects of the reaction of the metal with water will be pronounced both in area and in volume.
It is a further object of this invention to treat a subterranean formation to remove waxes from it by introducing into the formation a wax solvent in which has been dispersed an agent which will react exothermally with water in the formation to heat up the wax solvent above the formation temperature to enable it more effectively to dissolve the waxes and assist the removal of them from the formation. 1
Other objects and advantages of this invention will become apparent as the description of it proceeds hereinafter.
As one illustrative embodiment of a reactive agent useful in this invention, a dispersion of sodium metal is made in a carrier which is inert to it. Preferably, although not necessarily, the carrier is a wax solvent and may be, for example, a crude oil, a highly aromatic petroleum fraction, or a refined petroleum product. 802 extracts of diesel fuel and S02 extracts of kerosene have been found to be especially effective as solvents of waxes found in oil wells and are suitable for the purpose of this invention. The sodium dispersion may be made by violently mixing the metal into the carrier by a mechanical agitator until the sodium is reduced to particle sizes which will remain dispersed. Particles ranging in size from sub-micron to 5 microns are desirable because this size range is advantageous for migrating into a subterranean formation. A particle size of less than 1 micron is preferable for this purpose. Dispersing aids or stabilizers, such as long-chain fatty acids, silicone oil or other suitable surface-active agents, may be added and the carrier and metal may be heated to aid the formation of the dispersion. Dispersing aids may be selected which also will affect the rate of reaction of the sodium with water, to control the rate at which heat is liberated by the reaction.
Instead of sodium metal, an alloy of sodium and potassium metals may be used. The proportions of metals in the alloy may be selected so that the alloy is a liquid at ordinary temperatures and the dispersion will be that of the liquid alloy in the liquid carrier. Under these circumstances, there is obviously no criticality of particle size of the liquid alloy for the best effect on the formation. Lithium, potassium, rubidium and cesium also may be used separately or in combination as the reactive agent.
In carrying out the steps of the present invention, the dispersion of alkali metal in its inert wax-solvent carrier may be introduced into the bore hole by one of several means. Care must be taken to remove all traces of water from the conduits through which the alkali metal dis persion is to be introduced, including the well tubing or casing down to the location of the oil-bearing formation. If, for example, the dispersion is to be introduced into the well through tubing, a slug of the water-free carrier for the dispersion is introduced into the tubing prior to plac- Patented July 16, 1957.
ing the dispersion in it, and the slug of carrier is forced down to the location of the formation to clear all water from the path to be taken by the dispersion. A quantity of alkali metal dispersion is then placed in the tubing, followed by another slug of the carrier alone. If it is necessary to do so, the final slug of carrier is placed under pressure to force the quantity of sodium dispersion down to the elevation of the formation. Sufiicient pressure is placed on the quantity of dispersion to cause it to migrate into the formation a predetermined distance. cases, the hydrostatic head of the products in the tube may be sufiicient for this purpose.
As the alkali metal distributes itself over the exposed face of and into the formation, it will contact the connate water therein and react with it to produce heat. The initial quantities of alkali metal will react with the water nearest the exposed face of the formation, causing that portion of the formation to be heated first. Subsequent particles of alkali metal migrating through the heated zone may become melted before they reach additional water with which to react. The melting of the alkali metal will aid it in progressing into the formation. Hence, the process of heating the formation in volume will continue until all of the alkali metal or water is used up. When it is desired to produce more heat than the available water in the formation will permit, additional water may be added from the surface, as required.
Another way of introducing the dispersion into the well is by the use of a proportioning pump. In this procedure, a liquid carrier is continuously pumped into the Well and predetermined proportions of a concentrated dispersion automatically are added to it from an appropriate tank to give the desired proportion of alkali metal at the location of the formation.
It is also within the concept of this invention that the alkali metal dispersion or a liquid alloy of alkali metals may be introduced into the bore hole in a sealed container which can be transported down to the elevation of the subterranean formation to be treated and then ruptured to release the reactive material. In this latter case, care must be taken to make sure the bore hole is substantially free from water at the location of the formation so that the reactive material will not all react in the bore hole before it can be forced into the formation.
Preferably, after the dispersion of sodium or other alkali metal or alkali metal alloy has been introduced into the formation, the well is shut-in for a time to insure reaction of the alkali metal with formation waters and the proper distribution of heat throughout the formation. For example, the well may be shut-in from 1 to 4 hours to produce the desired result. While the formation and the reaction products are still warm, the well is placed on production, and the Waxes dissolved in the carrier, as well as the reaction products of the alkali metal with the formation water, will be produced out of the well to free the formation for the subsequent production of petroleum.
As an illustrative example of some of the conditions which apply to the practice of this invention, the relationships which follow from the use of a dispersion of sodium metal in a Wax solvent liquid hydrocarbon carrier, as de scribed hereinbefore, will be set forth. It will be apparent that such a dispersion will have many of the physical characteristics of a liquid.
The volume of solution required per linear foot of treated formation for injection to a distance rz feet from the center of a Well radius rw feet may be obtained from the formula Gallons solution per foot of formation =0.24 (rz rz f In some 1 4 proach quantitative reaction with the connate water in the formation will be given by the equation 13s., Sw
where Sw is the percent of pore space filled with water.
The theoretical temperature increase in degree F. from the reaction under adiabatic conditions may be determined from the relationship F. temperature rise=0.066f (100-Sw) (lb. Na per gal. solvent) (HI) F.=0.85 f Sw (IV) again assuming no heat loss to surrounding rock or fluids. The following calculations illustrate for a hypothetical case the values that result from the above relationships: Let
Pounds sodium per gallon of solvent: (II) By substituting the numerical values in the equations set forth above, it can be determined from Equation I that it will require 18 gallons of dispersion per foot of formation to fill it to a distance 2 feet from the center of the hole.
From Equation II above, it can be determined that there will be required 3.25 pounds of sodium per gallon of carrier to achieve quantitative reaction with the connate water in the formation under the conditions specified.
From Equation III it can be determined that the theoretical temperature rise of the treated portion of the formation when a dispersion of one pound of sodium metal per gallon of dispersion is used will be F. maximum.
From Equation IV, it can be determined that the temperature rise resulting from using enough sodium for quantitative reaction with the water present will be 340 F. maximum.
The above temperature increases are theoretical and are not obtained in practice since some heat transfer must exist in the formation. Also, there is the possibility that not all of the dispersed sodium will penetrate into the formation or be reacted with water therein. Therefore, it is desirable to adopt a factor which will depend on the particular formation and hole conditions to decrease the theoretical calculated amount to a value which will be encountered practically in the field. This factor will be between 0.1 and 0.5, depending on specific conditions indicated above. However, even the 0.1 factor indicates there will be an appreciable temperature rise in the subterranean formation-following the practice of this invention.
It will be apparent that heating the formation in the manner set forth herein will have several beneficial effects in freeing it from deleterious waxy deposits. The heat of reaction of the alkali metal with the formation Water will, in itself, cause melting of some such deposits and the subsequent freeing of the formation. Just as important as this effect, however, is that created by raising the temperature of the wax solvent which is a carrier for the dispersed reactive metal. As the temperature of the solvent is raised, it becomes increasingly more effective to dissolve the waxes from the formation and thereby free it for production of oil. Since the dispersion, including both the wax solvent and the reactive agent, has been caused to migrate into the formation in depth, there will take place more than a heating and cleaning of merely the exposed surface of the formation, but the effect of heat and solvent will reach beyond the exposed surface to remove the waxes that have been deposited in the pore spaces and interstices at some distance from the face.
It will be obvious that the method of this invention can be practiced by other specific apparatus and agents than those set forth above as exemplary embodiments without departing from the inventive concept, and it is intended to include all modifications and variations which fall within the scope of the appended claims.
I claim:
1. The method of treating an oil well which comprises introducing into said well a dispersion of alkali metals in a liquid wax solvent carrier which is inert to said metals, placing said dispersion under pressure to force a portion of said alkali metals and said liquid wax solvent carrier into an oil-bearing formation to allow said alkali metal to react with the water contained within said formation to raise the temperature of said wax solvent, reacting the remaining portion of said alkali metals with water in said oil well, and removing the reaction products and wax solvent carrier and dissolved waxes from said well while the temperature of said products and carrier is above the normal temperature of said well.
2. The process of treating an oil well which comprises introducing into said well a particulated alkali metal having particles ranging in size from sub-micron to microns and contained in a wax solvent fluid carrier Which is inert to it, placing said carrier and particulated alkali metal under pressure in the well to force some of said particles and wax solvent to migrate into an oil-bearing formation to allow said alkali metal to react with the water contained therein and heat said formation and said wax solvent, and removing the products of reaction and dissolved waxes from said oil well.
3. The process for treating an oil-bearing formation penetrated by a well bore to free said formation of waxy deposits which comprises introducing into said well bore a dispersion of sodium in a liquid wax solvent carrier for it, positioning said dispersion in said carrier at the location of said oil-bearing formation and placing said dispersion and carrier under a pressure greater than the pressure existing in said formation to force said dispersion and carrier into said formation to allow said sodium to react with the water contained within said formation, and thereafter removing the products of reaction and the wax solvent and dissolve the waxes from said formation.
4. The process for treating an oil-bearing formation in an oil well to free it of waxy deposits comprising introducing a quantity of a liquid which is inert to sodium into the well bore, immediately thereafter introducing a predetermined amount of a dispersion of sodium in said liquid into said well bore, immediatelythereafter introducing a further quantity of said liquid into said well bore, transporting said quantities of liquid and the included amount of said dispersion of sodium to a position where said dispersion of sodium is at the location of said formation, and at said location placing said dispersion of sodium under a pressure greater than the pressure in said formation to cause particles of the dispersed sodium and a portion of said liquid to enter said formation to allow said sodium to react with the water contained therein and subsequently removing said liquid and the reaction products of said sodium from the well bore.
5. The process for treating an oil well which comprises introducing into said well a dispersion of sodium metal in a liquid solvent for wax, placing said dispersion under pressure to force particles of the sodium metal and portions of said solvent into an oil-bearing formation, to allow said sodium metal to react with water in said well and within said formation, and thereafter removing the products of the reaction together with the wax solvent and dissolved waxes from said oil well.
6. A method for treating an oil well which comprises introducing a liquid alloy consisting essentially of sodium metal and potassium metal into said oil well, placing said liquid alloy under pressure to force said alloy into an oilbearing formation, to allow said alloy to react with water within said formation, and removing the products of reaction from said oil well.
7. A method of treating an oil-bearing formation penetrated by a well bore to free said formation of waxy deposits and water which comprises removing substantially all the water from the portion of said well bore adjacent the formation to be treated, introducing into said substantially water-free portion of said well bore an aromatic wax solvent inert to alkali metal and containing dispersed therein alkali metalparticulated into sizes ranging from submicron to five micron, placing said wax solvent dispersion under pressure sufliciently greater than the pressure in said formation to force said solvent dispersion substantially into said formation to allow said alkali metal to react with the water in said formation and to raise substantially the temperature of the wax solvent within said formation, whereby the solvent power of the solvent wax is greatly increased, and removing the reaction products of alkali metal with water in the solvent and dissolved waxes from said formation and said well bore while the temperature of said products, solvent and dissolved waxes is appreciably above the normal temperature of said formation.
References Cited in the file of this patent UNITED STATES PATENTS 2,089,479 Herbsman Aug. 10, 1937 2,218,306 Austerman Oct. 15, 1940 2,672,201 Lorenz Mar. 16, 1954 OTHER REFERENCES Reistle: ParafiinBureau of Mines Bulletin 348, pages 83 to 84. Govt. Printing Office, 1932.
UNITED STATES PATENT OFFICE Certificate of Correction Patent No. 2,799,342 July 16, 1 957 A 13:- W Irving Fatt "9 Is is hereby certified that error appears in the printed specification of above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
Column 3, line 68, after well and before radius insert of; same column, lines 71 and 72, the formula should read as shown below instead of as in the patent- Gallons solution per foot of formation =0.24 (71 -73 f (I) Signed and sealed this 24th day of September 1957.
[SEAL] Attest: l
KARL H. AXLINE, ROBERT C. WATSON, Attestimg Ofiicer. 'ommissioner of Patents.
Claims (1)
1. THE METHOD OF TREATING ON OIL WELL WHICH COMPRISES INTRODUCING INTO SAID WELL A DISPERSION OF ALKALI METALS IN A LIQUID WAX SOLVENT CARRIER WHICH IS INERT TO SAID METALS, PLACING DISPERSION UNDER PRESSURE TO FORCE A PORTION OF SAID ALKALI METALS AND SAID LIQUID WAX SOLVENT CARRIER INTO AN OIL-BEARING FORMATION TO ALLOW SAID ALKALI METAL TO REACT WITH THE WATER CONTAINED WITHIN SAID FORMATION TO RAISE THE TEMPERATURE OF SAID SOLVENT, REACTING THE REMAINING PORTION OF SAID ALKALI METALS WITH WATER IN SAID OIL WELL, AND REMOVING THE REACTION PRODUCTS AND WAX SOLVENT CARRIER AND DISSOLVED WAXES FROM SAID WELL WHILE THE TEMPERATURE OF SAID PRODUCTS AND CARRIER IS ABOVE THE NORMAL TEMPERATURE OF SAID WELL.
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US446973A US2799342A (en) | 1954-07-30 | 1954-07-30 | Process for treating oil well formations |
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US446973A US2799342A (en) | 1954-07-30 | 1954-07-30 | Process for treating oil well formations |
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Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2889884A (en) * | 1956-10-12 | 1959-06-09 | Gulf Research Development Co | Process for increasing permeability of oil bearing formation |
US2943681A (en) * | 1957-04-29 | 1960-07-05 | Michael W Barrett | Fracturing using calcium carbide |
US3129760A (en) * | 1957-12-30 | 1964-04-21 | Gambill Marvin | Hot caustic treatment of earth formations |
US3279541A (en) * | 1965-08-20 | 1966-10-18 | Halliburton Co | Method for removing paraffinic and asphaltic residues from wells |
US4007791A (en) * | 1975-08-07 | 1977-02-15 | J. Carroll Baisch | Method for recovery of crude oil from oil wells |
US4085799A (en) * | 1976-11-18 | 1978-04-25 | Texaco Inc. | Oil recovery process by in situ emulsification |
US4399868A (en) * | 1981-09-30 | 1983-08-23 | Shell Oil Company | Unplugging brine-submerged perforations |
US5139088A (en) * | 1989-09-06 | 1992-08-18 | Shell Oil Company | Method of inhibiting asphalt precipitation in an oil production well |
US7946342B1 (en) * | 2009-04-30 | 2011-05-24 | The United States Of America As Represented By The United States Department Of Energy | In situ generation of steam and alkaline surfactant for enhanced oil recovery using an exothermic water reactant (EWR) |
WO2014049021A1 (en) * | 2012-09-27 | 2014-04-03 | Wintershall Holding GmbH | Method for the recovery of natural gas and natural gas condensate from subterranean gas condensate reservoirs and flowable compositions (fz) for use in said method |
WO2014167011A1 (en) * | 2013-04-10 | 2014-10-16 | Wintershall Holding GmbH | Flowable composition (fz) for the thermal treatment of cavities |
US9376901B2 (en) | 2011-09-20 | 2016-06-28 | John Pantano | Increased resource recovery by inorganic and organic reactions and subsequent physical actions that modify properties of the subterranean formation which reduces produced water waste and increases resource utilization via stimulation of biogenic methane generation |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2089479A (en) * | 1936-05-26 | 1937-08-10 | Ind Patents Ltd | Method of cleaning-out oil wells |
US2218306A (en) * | 1938-06-03 | 1940-10-15 | Austerman Karl | Method of treating oil wells |
US2672201A (en) * | 1950-08-19 | 1954-03-16 | Pure Oil Co | Increasing production of oil wells |
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1954
- 1954-07-30 US US446973A patent/US2799342A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2089479A (en) * | 1936-05-26 | 1937-08-10 | Ind Patents Ltd | Method of cleaning-out oil wells |
US2218306A (en) * | 1938-06-03 | 1940-10-15 | Austerman Karl | Method of treating oil wells |
US2672201A (en) * | 1950-08-19 | 1954-03-16 | Pure Oil Co | Increasing production of oil wells |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2889884A (en) * | 1956-10-12 | 1959-06-09 | Gulf Research Development Co | Process for increasing permeability of oil bearing formation |
US2943681A (en) * | 1957-04-29 | 1960-07-05 | Michael W Barrett | Fracturing using calcium carbide |
US3129760A (en) * | 1957-12-30 | 1964-04-21 | Gambill Marvin | Hot caustic treatment of earth formations |
US3279541A (en) * | 1965-08-20 | 1966-10-18 | Halliburton Co | Method for removing paraffinic and asphaltic residues from wells |
US4007791A (en) * | 1975-08-07 | 1977-02-15 | J. Carroll Baisch | Method for recovery of crude oil from oil wells |
US4085799A (en) * | 1976-11-18 | 1978-04-25 | Texaco Inc. | Oil recovery process by in situ emulsification |
US4399868A (en) * | 1981-09-30 | 1983-08-23 | Shell Oil Company | Unplugging brine-submerged perforations |
US5139088A (en) * | 1989-09-06 | 1992-08-18 | Shell Oil Company | Method of inhibiting asphalt precipitation in an oil production well |
US7946342B1 (en) * | 2009-04-30 | 2011-05-24 | The United States Of America As Represented By The United States Department Of Energy | In situ generation of steam and alkaline surfactant for enhanced oil recovery using an exothermic water reactant (EWR) |
US9376901B2 (en) | 2011-09-20 | 2016-06-28 | John Pantano | Increased resource recovery by inorganic and organic reactions and subsequent physical actions that modify properties of the subterranean formation which reduces produced water waste and increases resource utilization via stimulation of biogenic methane generation |
WO2014049021A1 (en) * | 2012-09-27 | 2014-04-03 | Wintershall Holding GmbH | Method for the recovery of natural gas and natural gas condensate from subterranean gas condensate reservoirs and flowable compositions (fz) for use in said method |
US9587472B2 (en) | 2012-09-27 | 2017-03-07 | Wintershall Holding GmbH | Process for producing natural gas and natural gas condensate from underground gas condensate deposits |
WO2014167011A1 (en) * | 2013-04-10 | 2014-10-16 | Wintershall Holding GmbH | Flowable composition (fz) for the thermal treatment of cavities |
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