US3917345A - Well stimulation for solution mining - Google Patents
Well stimulation for solution mining Download PDFInfo
- Publication number
- US3917345A US3917345A US422239A US42223973A US3917345A US 3917345 A US3917345 A US 3917345A US 422239 A US422239 A US 422239A US 42223973 A US42223973 A US 42223973A US 3917345 A US3917345 A US 3917345A
- Authority
- US
- United States
- Prior art keywords
- formation
- pressure
- fluid
- well
- copper
- 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
- 238000005065 mining Methods 0.000 title description 18
- 230000000638 stimulation Effects 0.000 title description 9
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 61
- 239000012530 fluid Substances 0.000 claims abstract description 54
- 238000000034 method Methods 0.000 claims abstract description 47
- 239000011435 rock Substances 0.000 claims abstract description 15
- 239000000243 solution Substances 0.000 claims description 38
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 31
- 229910052802 copper Inorganic materials 0.000 claims description 31
- 239000010949 copper Substances 0.000 claims description 31
- 230000008569 process Effects 0.000 claims description 26
- 238000002386 leaching Methods 0.000 claims description 17
- 229910052951 chalcopyrite Inorganic materials 0.000 claims description 12
- DVRDHUBQLOKMHZ-UHFFFAOYSA-N chalcopyrite Chemical compound [S-2].[S-2].[Fe+2].[Cu+2] DVRDHUBQLOKMHZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000003929 acidic solution Substances 0.000 claims description 10
- 238000011065 in-situ storage Methods 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052683 pyrite Inorganic materials 0.000 claims description 4
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 claims description 4
- 239000011028 pyrite Substances 0.000 claims description 4
- 239000007800 oxidant agent Substances 0.000 claims description 3
- 239000012670 alkaline solution Substances 0.000 claims description 2
- 230000006872 improvement Effects 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 1
- 235000011149 sulphuric acid Nutrition 0.000 claims 1
- 230000035699 permeability Effects 0.000 abstract description 14
- 238000009792 diffusion process Methods 0.000 abstract description 3
- 238000005755 formation reaction Methods 0.000 description 50
- 206010017076 Fracture Diseases 0.000 description 45
- 208000010392 Bone Fractures Diseases 0.000 description 13
- 239000002360 explosive Substances 0.000 description 9
- 229910052500 inorganic mineral Inorganic materials 0.000 description 9
- 239000011707 mineral Substances 0.000 description 9
- 239000002002 slurry Substances 0.000 description 7
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 description 6
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000011084 recovery Methods 0.000 description 5
- 239000004576 sand Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910001779 copper mineral Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000011800 void material Substances 0.000 description 3
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005474 detonation Methods 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 238000009533 lab test Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical class [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 241000184339 Nemophila maculata Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 1
- OMZSGWSJDCOLKM-UHFFFAOYSA-N copper(II) sulfide Chemical compound [S-2].[Cu+2] OMZSGWSJDCOLKM-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000012508 resin bead Substances 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 229910052569 sulfide mineral Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- JFALSRSLKYAFGM-UHFFFAOYSA-N uranium(0) Chemical compound [U] JFALSRSLKYAFGM-UHFFFAOYSA-N 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
Classifications
-
- 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
- E21B43/28—Dissolving minerals other than hydrocarbons, e.g. by an alkaline or acid leaching agent
- E21B43/283—Dissolving minerals other than hydrocarbons, e.g. by an alkaline or acid leaching agent in association with a fracturing process
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/80—Compositions for reinforcing fractures, e.g. compositions of proppants used to keep the fractures open
Definitions
- ABSTRACT Methods for increasing the permeability of a subterranean igneous rock formation penetrated by at least one well where a hydraulic fluid is injected into the formation at a pressure sufficient to cause difiusion into the natural fractures thereof and thus increase the cross-sectional area thereof, maintaining the pressure and injecting a second fluid which results, by the use thereof, in substantially maintaining the increased cross-sectional area after the pressure is reduced.
- This invention relates to the treatment of underground depositbearing formations. More particularly, it relates to a method for increasing the permeability of such underground formations to enhance or stimulate the recovery of the desired deposits therefrom.
- the fracture may extend outside the treatment zone to a porous formation which creates a problem of leakage from the solution mining operation.
- the objects of the present invention are preferably accomplished by a process in which prior to any hydrometallurgical operation being conducted on the underground deposits, there is injected into the formation, via the well, a hydraulic fluid at a pressure sufficient to cause diffusion of said fluid into the natural fractures of the formation but below pressure at which new fractures would be formed in the formation and which consequently causes the fracture to increase in at least the cross-sectional area thereof. While maintaining said pressure, a second fluid is injected into said natural fractures via said well.
- the second fluid is of such character that it causes the increased cross-sectional area of the natural fractures to be substantially maintained after the pressuie is reduced.
- the permeability of the formation can be substantially increased without incurring any of the prior art' disadvantages including high pressures need for initiating new fractures which present engineering and. safety problems.
- the natural fractures of the formation are treated to produce the desired end result and there is no need for conducting a fracturing operation, i.e. to produce new fractures in the formation, which requires substantial time, money and effort.
- the use of explosives implanted in crevices, cracks, or fissures is common in mining and quarrying operations. Such explosives have included both solid and liquid-type explosives.
- Explosive fracturing by the detonation of an explosive device in a wellbore also requires a subsequent clean up operation before recovery of operations can be begun at that wellsite, increasing both the time and expense involved in such a treating action. Explosive fracturing also presents numerous safety problems; it has been experienced in the past that several people have been killed in conjunction with the utilization of explosives for carrying out the desired end result; i.e., fracturing underground formations.
- the hydraulic fluid is any liquid which is capable of being pumped at below fracturing pressures. It is to be understood that the term hydraulic fluid is not intended to mean that it creates new fractures, since the inventive concept herein is the use of such fluid (and a second fluid hereinafter defined) to dilate natural fractures without creating any substantial new fractures.
- fluids known in the art as fracturing fluids or hydraulic fracturing fluids may be used without departing from the scope of the invention, it being understood that the process claimed herein operates below the fracturing pressure of the ore body.
- a solvent for the metal values in the formation can be used, preferably the initial opening will be made with a non-solvent.
- suitable fluids include alcohols and glycols, water and brine or any other organic or inorganic liquid which meets the requirements of being pumpable at the necessary pressure.
- the preferred fluid will be water or water saturated with the material of the formation being treated. It is within the skill of the art to add thickening agents, fluid loss additives, corrosion inhibitors, bactericides and the like to the fluid when desired.
- the second fluid which is used, in the present invention processes is either an aqueous slurry containing a propping agent or a solution, acidic or alkaline, hereinafter referred to as reactive solution, which is capable of reacting with the rock formation via corrosion, dissolution and/or oxidation to increase at least the crosssectional area of the natural fractures, and in some cases the length thereof by relatively short distances.
- Suitable propping agents include sand, glass beads, resin beads such as polyethylene or other polymeric beads, metallic pellets such as aluminum pellets, walnut hulls or shells, ceramics, and the like.
- the propping agent can be added initially with the hydraulic or fracturing fluid, but will preferably not be added until the opening is increased.
- the particle size of the propping agent since the purpose thereof is to provide effective propping and/or to prevent sealing of the natural fractures.
- a US. Sieve Size of between about 12 and 40 mesh would be quite suitable. This is not a critical feature and thus the mesh size should be determined based upon the material used, solution flow rates desired, economics and the like.
- the quantity of the propping agent in the aqueous slurry is ascertainable in a similar fashion with the only restraint being that the slurry must be pumpable.
- Sand for example, can be used in a weight range of about 1 to percent based on the total weight of said slurry.
- the reactive solution i.e. one of the above described second fluids, can be any acidic solution which has a pH of less than 6.5, preferably less than 2.0 and more preferably in the range of from about 0.5 to about 1.5 and which is reactive with the rock formation.
- the acids which can be used include, without limitation, I-IF, HCl, H 80 and mixtures thereof.
- Mud acid i.e. an aqueous solution containing 3% by weight HF and 13% by weight HCl, is a preferred second fluid.
- the acidic solution may also comprise or contain an oxidizing agent such as water soluble ferric salts like ferric sulfate. For example, see US. Pat. No. 3,574,599.
- Another preferred second fluid is a mixture of H SO and Fe (SO.,) a one molar solution and one-half molar solution respectively.
- the reactive solution may also be alkaline such as an ammoniacal solution.
- alkaline such as an ammoniacal solution.
- the pressure used to pump the hydraulic or fracturing fluid and/or the second fluid into the natural fractures is any pressure which does not cause any substantial new fracture formation and is usually less than about 1.0 pounds per square inch gauge (psig) per foot of well depth.
- psig pounds per square inch gauge
- the pressures can easily be within a range of about 1,000 psig to about 10,000 psig with wells of 1,000 to 10,000 feet deep. It is to be understood then that the pressure is a critical feature of the present invention in order to obtain the desired end results.
- a hydraulic or fracturing fluid is placed in a well penetrating the formation to be treated, optionally through the piping, adjacent and in contact with the face of the formation to be treated.
- packing is employed to isolate and confine the fracturing fluids to a portion of the well exposing the formation to be treated.
- Pressure is then applied via the hydraulic fluid so as to build up the pressure on the formation exposed to the hydraulic fluid to a value great enough to cause diffusion into the natural fractures.
- the time required to pump the hydraulic fluid will depend upon several variables including, without limitation, initial permeability, size of formation being treated, type fluid used and the like.
- the pump pressure indicates a pressure just below fracturing pressure of the formation for the depth of the well, then the second fluid is injected for a sufficient period of time for the propping agents to be positioned or for the reacting solution to react with the sides of the fractures. Again, these times will vary depending upon several variables and can range, for example, between about 30 minutes to about 10 hours.
- the processes of the present invention are uniquely effective in conjunction with the in-situ mining of underground igneous rock formations which contain copper metal values in the form of chalcopyrite and pyrite ores. It has been found that the stimulation of a low permeability deposit is an important factor for an economically viable in-situ mining operation. In the particular case relating to the underground (or solution) mining of chalcopyrite and pyrite ores, this stimulation permits the leaching solvent to contact more of the copper minerals, thus increasing both the leach efficiency and copper loadings. Both of these parameters are critical for economically mining deep-lying low grade copper ores by in-situ mining techniques.
- the copper leaching solution is injected in order to subsequently recover the copper values.
- the copper leaching procedures can be carried out in any manner known to those skilled in the art of in-situ mining such as those procedures described in US. Pat. Nos.
- the stimulation process can be'used at any time where one so desires.
- the hydraulic fluid' is used as a pretreatment of the formation or'deposit.
- thescope production wells be drilledin offsettingline patterns so 1 as-to form a line drive mechanism within the copper formation.
- the distance between the injection and production wells will be from to 1,000 feet, with particular. depth, thickness, permeability, porosity, water saturation of theformation, andeconomic value of the copper mineral contained therein being the engineering constraints upon which-the design of the solution mining patterns are based. Therefore,-through patterned well completionjn the copper formation, the process may be used sequentially across the copper deposit through aseries of line drive wells or concentric pattern wells so that the entire copper deposit maybe leached.
- EXAMPLE I An orebody 100 acres in area and averagingSOQ feet in thickness lies at an average depth of 4,000 feet below the surface of the earth in Arizona. Samples of the ore shows that it is composed primarily of granitic igneous rock and that it contains chalcopyriteas the principal copper mineral. The ore samples also show that it contains approximately 1.4 weight percent chalcopyrite and that the total copper content of the'ore averages 0.5 percent. The volume of ore in the deposit is, therefore, l0 acre-feet or 4.356 X 10 cubic feet. The specific gravity of the granitic ore is 2.6. Therefore, the total weight of the ore in the deposit is 3.54 X 10 tons, and the copper content of the ore body is 3.54 X 10' pounds.
- Approximately 5 wells are drilled into the ore body in an array such as to provide a five-spot pattern, and the wells are completed (sealed and cased to 4,000 feet) such that fluids may be either injected or produced from individual wells.
- the void volume within the randomly-oriented fracture system is equivalent to 2 percent of the bulk ore volume, that the fracture spacing averages 6 inches, and that the permeability of the ore body to liquid averages about millidarcys.
- Petrographic examination of core samples taken from the ore body shows that about 2 percent of the rock surface area exposed by the fractures is covered by the chalcopyrite mineral and that the rock matrix bounded by the fracture system is substantially cubical in configuration.
- the total surface area of'ore exposed by the fracture network is equal to 12/4.356 X 10 or 5.227 X 10 square feet.
- the surface area of the chalcopyrite mineral exposed by'the fracture system is equal to 2 percent of the total surface area, or 1.045 X 10 square feet.
- ferric sulfate solutions will dissolve copper from the chalcopyrite of the ore body at a rate equal to 0.0002 pound of copper per square foot of chalcopyrite surface area per day.
- the initial maximum rate of copper production attainable from the ore body by in-situ leaching with ferric sulfate would be 0.002 X 1.045 X 10 209,000 pounds of copper per day.
- the laboratory tests also showed that, by allowing a 0.4 molar solution of ferric sulfate to react completely with the chalcopyrite and other minerals in the ore, a pregnant leaching solution containing 3.0 pounds of copper per barre'l(42 gallons) could be obtained.
- the 0.4 molar ferric sulfate solution in order to supply 0.4 molar ferric'sulfate solution to the ore body at the optimum rate; i.e., at the rate sufficient to produce the maximum amount of copper and at the same time allow total reaction of the ferric iron, the 0.4 molar ferric sulfate solution must be injected initially at a rate equal to 69,700 barrels/day.
- the required average residence time for the solution within the ore body is fixed by the injection rate and the void volume of the ore body;
- the wells are operated for a sufficient period of time to reach equilibrium and the copper produced averages about 187,000 pounds per day.
- Example II Example I above is repeated in toto with the exception that mud acid is used in place of the aqueous slurry of sand in order to enlarge the natural fractures. Substantially the same magnitude of increase in copper production is obtained as that obtained using said sand slurry.
- Examples I and II have been described as applicable to the copper sulfide ores, it should be understood that the process is also applicable to ores bearing native copper and also to ores of copper oxides and sili' cates where the copper is present in the cuprous valence state.
- the copper is present in its elemental or lower valence state, it is susceptible to oxidation by ferric iron to form solutions of cupric sulfate.
- the leaching solution will be injected through a well, permitted to remain in contact with the ore body for a period of time, and then withdrawn through the same well.
- the pregnant leaching solution is then passed to a copper recovery stage, a regeneration stage and ultimately reinjected.
- the hydraulic fluid is water which is injected into said well of from 1,000 feet to 10,000 feet deep at a pressure of from about 1,000 psig to about 10,000 psig, wherein said pressure is less than about 1.0 psig per foot of well depth, and below the pressure producing new fractures in the formation.
- said second fluid is an acidic solution which is capable of reacting with said igneous rock to increase at least the cross-sectional area of said natural fractures.
- said acidic solution comprises a mixture of HF and HCl.
- said second fluid is selected from the group consisting of propping agents, acidic solutions, alkaline solutions, oxidizing agents and mixtures thereof.
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- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Chemical & Material Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Mining & Mineral Resources (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- Geochemistry & Mineralogy (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
Claims (8)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US422239A US3917345A (en) | 1973-12-06 | 1973-12-06 | Well stimulation for solution mining |
CA209,865A CA1000192A (en) | 1973-12-06 | 1974-09-24 | Well stimulation for solution mining |
ZA00746126A ZA746126B (en) | 1973-12-06 | 1974-09-26 | Well stimulation for solution mining |
AU73828/74A AU488201B2 (en) | 1973-12-06 | 1974-10-01 | Well stimulation for solution mining |
US05/604,869 US4342484A (en) | 1973-12-06 | 1975-08-14 | Well stimulation for solution mining |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US422239A US3917345A (en) | 1973-12-06 | 1973-12-06 | Well stimulation for solution mining |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US05/604,869 Division US4342484A (en) | 1973-12-06 | 1975-08-14 | Well stimulation for solution mining |
Publications (1)
Publication Number | Publication Date |
---|---|
US3917345A true US3917345A (en) | 1975-11-04 |
Family
ID=23673983
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US422239A Expired - Lifetime US3917345A (en) | 1973-12-06 | 1973-12-06 | Well stimulation for solution mining |
Country Status (3)
Country | Link |
---|---|
US (1) | US3917345A (en) |
CA (1) | CA1000192A (en) |
ZA (1) | ZA746126B (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4345652A (en) * | 1979-12-28 | 1982-08-24 | Institut Francais Du Petrole | Process for improving the permeability of ground formations, adapted to the production of high temperature geothermic energy |
US4393933A (en) * | 1980-06-02 | 1983-07-19 | Standard Oil Company (Indiana) | Determination of maximum fracture pressure |
US4630868A (en) * | 1979-05-11 | 1986-12-23 | Terra Tek, Inc. | Process for solution mining |
US6059034A (en) * | 1996-11-27 | 2000-05-09 | Bj Services Company | Formation treatment method using deformable particles |
US6330916B1 (en) | 1996-11-27 | 2001-12-18 | Bj Services Company | Formation treatment method using deformable particles |
US6364018B1 (en) | 1996-11-27 | 2002-04-02 | Bj Services Company | Lightweight methods and compositions for well treating |
US6439309B1 (en) | 2000-12-13 | 2002-08-27 | Bj Services Company | Compositions and methods for controlling particulate movement in wellbores and subterranean formations |
US6508305B1 (en) | 1999-09-16 | 2003-01-21 | Bj Services Company | Compositions and methods for cementing using elastic particles |
US20040014608A1 (en) * | 2002-07-19 | 2004-01-22 | Nguyen Philip D. | Methods of preventing the flow-back of particulates deposited in subterranean formations |
US6749025B1 (en) | 1996-11-27 | 2004-06-15 | Bj Services Company | Lightweight methods and compositions for sand control |
US6772838B2 (en) | 1996-11-27 | 2004-08-10 | Bj Services Company | Lightweight particulate materials and uses therefor |
US20050028979A1 (en) * | 1996-11-27 | 2005-02-10 | Brannon Harold Dean | Methods and compositions of a storable relatively lightweight proppant slurry for hydraulic fracturing and gravel packing applications |
WO2012083463A1 (en) * | 2010-12-22 | 2012-06-28 | Dusseault Maurice B | Multi-stage fracture injection process for enhanced resource production from shales |
US20150129211A1 (en) * | 2010-12-22 | 2015-05-14 | Maurice B. Dusseault | Multi-stage fracture injection process for enhanced resource production from shales |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US965714A (en) * | 1910-02-23 | 1910-07-26 | James S Island | Process for extracting or separating precious values from ores. |
US2563623A (en) * | 1951-08-07 | scott | ||
US3086760A (en) * | 1960-05-25 | 1963-04-23 | Fmc Corp | Method of creating an underground communication |
US3370887A (en) * | 1966-04-05 | 1968-02-27 | Continental Oil Co | Hole preparation for fracturing solution mining wells |
-
1973
- 1973-12-06 US US422239A patent/US3917345A/en not_active Expired - Lifetime
-
1974
- 1974-09-24 CA CA209,865A patent/CA1000192A/en not_active Expired
- 1974-09-26 ZA ZA00746126A patent/ZA746126B/en unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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US2563623A (en) * | 1951-08-07 | scott | ||
US965714A (en) * | 1910-02-23 | 1910-07-26 | James S Island | Process for extracting or separating precious values from ores. |
US3086760A (en) * | 1960-05-25 | 1963-04-23 | Fmc Corp | Method of creating an underground communication |
US3370887A (en) * | 1966-04-05 | 1968-02-27 | Continental Oil Co | Hole preparation for fracturing solution mining wells |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4630868A (en) * | 1979-05-11 | 1986-12-23 | Terra Tek, Inc. | Process for solution mining |
US4345652A (en) * | 1979-12-28 | 1982-08-24 | Institut Francais Du Petrole | Process for improving the permeability of ground formations, adapted to the production of high temperature geothermic energy |
US4393933A (en) * | 1980-06-02 | 1983-07-19 | Standard Oil Company (Indiana) | Determination of maximum fracture pressure |
US20050028979A1 (en) * | 1996-11-27 | 2005-02-10 | Brannon Harold Dean | Methods and compositions of a storable relatively lightweight proppant slurry for hydraulic fracturing and gravel packing applications |
US6059034A (en) * | 1996-11-27 | 2000-05-09 | Bj Services Company | Formation treatment method using deformable particles |
US6330916B1 (en) | 1996-11-27 | 2001-12-18 | Bj Services Company | Formation treatment method using deformable particles |
US6364018B1 (en) | 1996-11-27 | 2002-04-02 | Bj Services Company | Lightweight methods and compositions for well treating |
US6749025B1 (en) | 1996-11-27 | 2004-06-15 | Bj Services Company | Lightweight methods and compositions for sand control |
US6772838B2 (en) | 1996-11-27 | 2004-08-10 | Bj Services Company | Lightweight particulate materials and uses therefor |
US6508305B1 (en) | 1999-09-16 | 2003-01-21 | Bj Services Company | Compositions and methods for cementing using elastic particles |
US6439309B1 (en) | 2000-12-13 | 2002-08-27 | Bj Services Company | Compositions and methods for controlling particulate movement in wellbores and subterranean formations |
US20040014608A1 (en) * | 2002-07-19 | 2004-01-22 | Nguyen Philip D. | Methods of preventing the flow-back of particulates deposited in subterranean formations |
US6877560B2 (en) | 2002-07-19 | 2005-04-12 | Halliburton Energy Services | Methods of preventing the flow-back of particulates deposited in subterranean formations |
WO2012083463A1 (en) * | 2010-12-22 | 2012-06-28 | Dusseault Maurice B | Multi-stage fracture injection process for enhanced resource production from shales |
US8978764B2 (en) | 2010-12-22 | 2015-03-17 | Maurice B. Dusseault | Multi-stage fracture injection process for enhanced resource production from shales |
US20150129211A1 (en) * | 2010-12-22 | 2015-05-14 | Maurice B. Dusseault | Multi-stage fracture injection process for enhanced resource production from shales |
US10001003B2 (en) * | 2010-12-22 | 2018-06-19 | Maurice B. Dusseault | Multl-stage fracture injection process for enhanced resource production from shales |
Also Published As
Publication number | Publication date |
---|---|
AU7382874A (en) | 1976-04-08 |
CA1000192A (en) | 1976-11-23 |
ZA746126B (en) | 1975-10-29 |
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Owner name: KENNECOTT MINING CORPORATION Free format text: CHANGE OF NAME;ASSIGNOR:KENNECOTT CORPORATION;REEL/FRAME:004815/0036 Effective date: 19870220 Owner name: KENNECOTT CORPORATION, 200 PUBLIC SQUARE, CLEVELAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:KENNECOTT MINING CORPORATION;REEL/FRAME:004815/0063 Effective date: 19870320 Owner name: KENNECOTT CORPORATION Free format text: CHANGE OF NAME;ASSIGNOR:KENNECOTT COPPER CORPORATION;REEL/FRAME:004815/0016 Effective date: 19800520 |
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