US3841705A - Stimulation of production well for in situ metal mining - Google Patents
Stimulation of production well for in situ metal mining Download PDFInfo
- Publication number
- US3841705A US3841705A US00401484A US40148473A US3841705A US 3841705 A US3841705 A US 3841705A US 00401484 A US00401484 A US 00401484A US 40148473 A US40148473 A US 40148473A US 3841705 A US3841705 A US 3841705A
- Authority
- US
- United States
- Prior art keywords
- ore
- ore body
- leach solution
- rubblized
- wells
- 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
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 47
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 30
- 239000002184 metal Substances 0.000 title claims abstract description 28
- 238000011065 in-situ storage Methods 0.000 title abstract description 15
- 238000005065 mining Methods 0.000 title description 7
- 230000000638 stimulation Effects 0.000 title description 4
- 238000002347 injection Methods 0.000 claims abstract description 48
- 239000007924 injection Substances 0.000 claims abstract description 48
- 239000000243 solution Substances 0.000 claims description 51
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 30
- 229910052802 copper Inorganic materials 0.000 claims description 30
- 239000010949 copper Substances 0.000 claims description 30
- 238000002386 leaching Methods 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 28
- 230000015572 biosynthetic process Effects 0.000 claims description 21
- 239000002360 explosive Substances 0.000 claims description 20
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000007789 gas Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 239000006185 dispersion Substances 0.000 claims description 2
- 239000002245 particle Substances 0.000 claims description 2
- 230000003381 solubilizing effect Effects 0.000 claims description 2
- 150000001455 metallic ions Chemical class 0.000 claims 2
- 238000005755 formation reaction Methods 0.000 description 19
- 239000012530 fluid Substances 0.000 description 13
- 229910052951 chalcopyrite Inorganic materials 0.000 description 10
- DVRDHUBQLOKMHZ-UHFFFAOYSA-N chalcopyrite Chemical compound [S-2].[S-2].[Fe+2].[Cu+2] DVRDHUBQLOKMHZ-UHFFFAOYSA-N 0.000 description 10
- 238000011084 recovery Methods 0.000 description 10
- 229910052500 inorganic mineral Inorganic materials 0.000 description 9
- 239000011707 mineral Substances 0.000 description 9
- 235000010755 mineral Nutrition 0.000 description 9
- 239000011435 rock Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 8
- 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 7
- 229910000360 iron(III) sulfate Inorganic materials 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 230000035699 permeability Effects 0.000 description 6
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 5
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 3
- 239000005751 Copper oxide Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910000431 copper oxide Inorganic materials 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000011800 void material Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000005474 detonation Methods 0.000 description 2
- 238000004880 explosion Methods 0.000 description 2
- 238000009533 lab test Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 238000005086 pumping Methods 0.000 description 2
- 238000012935 Averaging Methods 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 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
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- -1 arsenide Chemical compound 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052948 bornite Inorganic materials 0.000 description 1
- 229910052947 chalcocite Inorganic materials 0.000 description 1
- 229910001779 copper mineral Inorganic materials 0.000 description 1
- 229910052955 covellite Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 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
- 230000002706 hydrostatic effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000000203 mixture Substances 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
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- XSOKHXFFCGXDJZ-UHFFFAOYSA-N telluride(2-) Chemical compound [Te-2] XSOKHXFFCGXDJZ-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
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
Definitions
- the invention is a process of in situ mining comprising the steps of rubblizing a portion of an ore body by detonating one or more strategically placed explosive devices to form a rubblized zone or chimney, injecting a leach solution into one or more injection wells, the injection well or wells being located in the ore body adjacent to but outside of the rubblized chimney, such that the leach solution will pass through the nonrubblized ore body removing the metal values therefrom and into the rubblized chimney, and recovering a pregnant leach solution from one or more production wells located within the rubblized zone or chimney.
- an ore body is solution mined in-situ by first injecting a lixiviant into the ore formation under pressure through an array of injection wells.
- the pregnant solution is then recovered from the formation through one or more production wells that has been stimulated with a nuclear or chemical explosion subsequent to the injection of the leaching solution.
- the explosive charge causes rubblization in the area of the production well, but not in the immediate area of the injection wells, such that the rubblization reduces the resistance to lixiviant flow into the production well to the extent that the pregnant solution can be withdrawn from the production well nearly as fast as leaching liquid can be injected into the ore formation.
- FIG. 1 shows one possible array for well placement, commonly known as the 5-spot pattern.
- FIG. 2 shows the rubblization around the centrally located production well and the flow of leaching solvent from the distant injection wells into the rubblized zone.
- the above situation is termed a production limited system because overall recovery of pregnant solution, and therefore recovery of leached metallic element, is dependent on how fast solution can be withdrawn from the production well.
- the present invention is anattempt to reach an injection limited system such that recovery of pregnant solution is limited by the amount of solution which can be injected into the formation. This situation would typically result in much greater productivity than the production limited system.
- FIG. 1 the ore body 13 is located and an array of injection wells 12 and production wells 11 are bored.
- the particular pattern shown in FIG. 1 is commonly known as a S-spot pattern which allows the nearest neighbor of any injection well to be a production well and vice versa. It is within the scope of the invention described herein that any other desired pattern of wells may be used.
- all the production wells 11 will be rubblized with a chemical or nuclear explosive device to provide a rubblized zone 14 around each production well.
- the area of rubblization 14 indicates the relative extent of the blast area with respect to the placement of the injection wells. It will be noticed here,
- the arrows around the rubblized area 14 indicate the direction of fluid flow from nearby injection wells.
- the injection wells may be between about feet up to about 700 feet from the boundaries of the rubblized chimney area 14. The distance between production and injection wells willdepend on permeability profile of the rock mass surrounding the chimney.
- the rubblized area surrounding the production wells 11 creates a of lower permeability thus resulting in the flow of fluid from the high permeability igneous rock surrounding the injection wells 12 toward the production wells 11 rather than a fluid flow into other areas of the ore body-where the fluid may be lost.
- the rubblized zone 2 causedby the nuclear or chemical explosion, does not extend to the injection wells 4 and 5.
- the nuclear chimney from the blast may extend upward from the ore formation 1 to a point above the water table 6.
- the invention relates to the recovery of metal values found in mineral formations located beneath the ,water table and, hence, the rubblized zone of the production well will be below the water table. This fact, in turn, means that the hydrostatic pressures beneath the water table contribute integrally to the flow properties of leaching solution into the production well.
- rubblized chimneys of desired geometric configurations can be formed by strategically placing and detonating the explosives in proper sequence. See U.S. Pat. No. 3,470,953.
- Explosive reaction mixtures may be formed in concentric regions in the ore body around the wellbore by alternately injecting a propping agent and then an explosive reaction mixture. Upon detonation of the concentric regions of explosive reaction mixtures, the resulting fractures propagate both outwardly into the ore body and inwardly toward the wellbore so as to enhance the subsequent recovery of metal values from both the fractured areas and the areas between the injection well or wells and the centrally located production well. For further details, see U.S. Pat. No. 3,593,793.
- the present invention of an in situ leaching process has particular application to copper ore deposits,for example chalcopyrite, chalcocite, covellite and bornite.
- copper ore deposits for example chalcopyrite, chalcocite, covellite and bornite.
- the process is not limited to recovering copper but can be used in recovering many other metallic elements from their ores.
- Of interest would be nickel, zinc, molybdenum, silver, gold and other valuable metals.
- the leaching solvent injected into the formation would typically be'water, sulfuric acid, and ferrous sulfate, in various proportions, together with an oxidizing agent.
- the oxidizing agent is preferably an oxygen-bearing gas such as air, oxygen and any and all mixtures thereof.
- the oxygen-bearing gas may be introduced into the ore body prior to, during, or subsequent to the leaching solution.
- the copper is leached from the ore as a sulfate, and is later recovered from the solution by electrolysis, or in a precipitation process using de-tinned iron to replace the copper in solution.
- the present invention provides for very efficient in situ leaching by an appropriate acid or alkaline liquid extractant, such as aqueous sulfuric acid of moderate strength, e.g., acid containing 0.5 to 30 percent, and preferably 2 to percent, H 80 by weight.
- aqueous sulfuric acid of moderate strength, e.g., acid containing 0.5 to 30 percent, and preferably 2 to percent, H 80 by weight.
- Such sulfuric acid is pumped into the injection well in the copper ore in quantity sufficient to provide therein about 20 to 80 pounds H 50 per ton of ore to be treated when such ore contains between about 0.5 and '2 percent copper by weight.
- the pressures developed in pumping the leach solution into the ore body may vary over a wide range.
- the injection pressure will be below the formation fracture pressure.
- Recovery of copper from the formation by such leaching should be between about 40 and 85 percent or more, e.g. 70 percent somewhat depending on proportion and strength of acid used, permeability of the formation, concentration of copper therein, etc.
- the metal When the metal is in the ore as a sulfide, arsenide, telluride or a sulfo-salt, it can be recovered from such a sulfide-type ore either by converting it by in situ oxidation to the oxide by blowing air underground and then extracting the oxide as described above.
- the nuclear explosives useable may range in yield from as little as 10 kiloton up to 2,000 kilotons, it being noted that the cost of such explosives is relatively independent of the energy yield. Consequently, the largest size device that can be employed at the given depth appropriate for a particular job is generally the most economical one.
- EXAMPLE I An embodiment of the invention as applied to the recovery of copper from a formation which contains copper oxide will next be described.
- the Copper ore deposit to be treated is a stratum 1,000 feet thick and has 2,000 feet of overburden above it. This stratum con tains copper in a concentration of about 1 percent in igneous gangue.
- a 50 kiloton thermo-nuclear explosive is placed in the formation through a well at a depth of 3,200 feet. When the well is sealed and the device detonated, a chimney approximately 650 feet high is created above the shot point. It is estimated that the chimney will have a diameter of about 265 feet and contain about 2 million tons of rubble. If it is found that additional copper ore need be caved down, this may be produced by placing or detonating a further nuclear device in the formation.
- Aqueous sulfuric acid having an H content of about 5 weight per cent is then pumped into the injection wells located some distance outside the rubblized chimney. Sufficient volume of acid of proper strength should be introduced into the injection wells to allow for the ultimate consumption of about 40 pounds H 80 per ton of broken rock treated in the process. After the acid is introduced in the injection wells it will percolate through the ore body and take some copper oxide into solution, which will accumulate as a body of liquid in the lower part of the chimney.
- the accumulation of pregnant leach solution in the chimney cavity can be pumped out through the production well located in the chimney.
- the copper is then recovered from the pregnant leach solution by known methods.
- EXAMPLE ll An ore body acres in area and averaging 100 feet in thickness lies at an average depth of 3,000 feet below the surface of the earth. Samples of the ore shows that it is composed primarily of granitic igenous rock and that it contains chalcopyrite as the principle 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, 10 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.
- Wells are drilled into the body in an array such that the well density is one per acre. Position of production wells is determined. Liquid slurry or nuclear explosives are strategically placed and detonated such that the injection well positions remain outside of the rubblized chimney area. By measurements on core samples and by injection and production tests on individual wells, it is determined that 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 25 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 surfaceto-volume ratio of the ore blocks bounded by the fractures is approximately equal to that for cubically shaped blocks, and the surface area to volume ratio for the ore blocks is equal to 6/L, where L is the length of the side of a cube. In this case L 0.5 feet, and the surface area to volume ratio is equal to 12 square feet/cubic foot.
- the total surface area of ore exposed by the fracture network is equal to 12 X 4.356 X 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.
- 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 of 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:
- This average residence time or the average time required for the fluid to traverse the ore body between injection and production wells, must be increased as the chalcopyrite mineral is depleted and the surface area of chalcopyrite exposed to the leaching solution diminishes.
- the optimum average residence time for the 0.4 molar ferric sulfate solution will be continuously increasing and may be substantially greater than the 22.2 days calculated as the optimum average residence time at the start of the operation.
- the injection and production rates should be approximately equal in order to minimize migration of fluids into or away from the ore body being subjected to the solution mining process.
- the average injection and production rates will be initially:
- the injection and production rates at individual wells may be varied as necessary to maintain an approximate overall balance between total injection and total production, and to maintain the residence time required for essentially complete reaction of the ferric iron in the leaching solution with the ore minerals.
- An improved process for recovering metal values by in-situ leaching an ore body located below the water table which comprises:
- rubblized zone is produced by detonating one or more strategically placed explosives in the ore body, said explosive selected from nuclear and chemical explosives.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Manufacture And Refinement Of Metals (AREA)
Abstract
Description
Claims (10)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00401484A US3841705A (en) | 1973-09-27 | 1973-09-27 | Stimulation of production well for in situ metal mining |
ZA00745723A ZA745723B (en) | 1973-09-27 | 1974-09-09 | Stimulation of production well for in situ metal mining |
AU73213/74A AU489035B2 (en) | 1973-09-27 | 1974-09-11 | Stimulation of production well for in situ metal mining |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00401484A US3841705A (en) | 1973-09-27 | 1973-09-27 | Stimulation of production well for in situ metal mining |
Publications (1)
Publication Number | Publication Date |
---|---|
US3841705A true US3841705A (en) | 1974-10-15 |
Family
ID=23587955
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US00401484A Expired - Lifetime US3841705A (en) | 1973-09-27 | 1973-09-27 | Stimulation of production well for in situ metal mining |
Country Status (2)
Country | Link |
---|---|
US (1) | US3841705A (en) |
ZA (1) | ZA745723B (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3894770A (en) * | 1974-06-12 | 1975-07-15 | Kennecott Copper Corp | Wellbore oxidation of lixiviants |
US3951458A (en) * | 1974-07-31 | 1976-04-20 | Kennecott Copper Corporation | Method of explosive fracturing of a formation at depth |
US4037657A (en) * | 1975-09-05 | 1977-07-26 | Lekas Mitchell A | Process for recovery of carbonaceous materials from subterranean deposits by in situ processing |
US4080419A (en) * | 1976-12-10 | 1978-03-21 | The United States Of America As Represented By The Secretary Of The Interior | Foam injection leaching process for fragmented ore |
US4125289A (en) * | 1976-10-28 | 1978-11-14 | Kennecott Copper Corporation | Method for in situ minefields |
US4239286A (en) * | 1973-07-26 | 1980-12-16 | E. I. Du Pont De Nemours And Company | In situ leaching of ore bodies |
US4249776A (en) * | 1979-05-29 | 1981-02-10 | Wyoming Mineral Corporation | Method for optimal placement and orientation of wells for solution mining |
US4381873A (en) * | 1980-08-12 | 1983-05-03 | Occidental Research Corp. | In situ roasting and leaching of sulfide minerals |
US20150260025A1 (en) * | 2014-03-14 | 2015-09-17 | Solvay Sa | Multi-well solution mining exploitation of an evaporite mineral stratum |
DE102021126656B3 (en) | 2021-10-14 | 2023-03-30 | Technische Universität Bergakademie Freiberg, Körperschaft des öffentlichen Rechts | Process for leaching metal-bearing ores using microorganisms |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3278233A (en) * | 1964-03-27 | 1966-10-11 | Mobil Oil Corp | In situ leaching of subterranean deposits |
US3490534A (en) * | 1968-04-02 | 1970-01-20 | Cities Service Oil Co | Treatment of water wells using a satellite well |
US3542131A (en) * | 1969-04-01 | 1970-11-24 | Mobil Oil Corp | Method of recovering hydrocarbons from oil shale |
-
1973
- 1973-09-27 US US00401484A patent/US3841705A/en not_active Expired - Lifetime
-
1974
- 1974-09-09 ZA ZA00745723A patent/ZA745723B/en unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3278233A (en) * | 1964-03-27 | 1966-10-11 | Mobil Oil Corp | In situ leaching of subterranean deposits |
US3490534A (en) * | 1968-04-02 | 1970-01-20 | Cities Service Oil Co | Treatment of water wells using a satellite well |
US3542131A (en) * | 1969-04-01 | 1970-11-24 | Mobil Oil Corp | Method of recovering hydrocarbons from oil shale |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4239286A (en) * | 1973-07-26 | 1980-12-16 | E. I. Du Pont De Nemours And Company | In situ leaching of ore bodies |
US3894770A (en) * | 1974-06-12 | 1975-07-15 | Kennecott Copper Corp | Wellbore oxidation of lixiviants |
US3951458A (en) * | 1974-07-31 | 1976-04-20 | Kennecott Copper Corporation | Method of explosive fracturing of a formation at depth |
US4037657A (en) * | 1975-09-05 | 1977-07-26 | Lekas Mitchell A | Process for recovery of carbonaceous materials from subterranean deposits by in situ processing |
US4125289A (en) * | 1976-10-28 | 1978-11-14 | Kennecott Copper Corporation | Method for in situ minefields |
US4080419A (en) * | 1976-12-10 | 1978-03-21 | The United States Of America As Represented By The Secretary Of The Interior | Foam injection leaching process for fragmented ore |
US4249776A (en) * | 1979-05-29 | 1981-02-10 | Wyoming Mineral Corporation | Method for optimal placement and orientation of wells for solution mining |
US4381873A (en) * | 1980-08-12 | 1983-05-03 | Occidental Research Corp. | In situ roasting and leaching of sulfide minerals |
US20150260025A1 (en) * | 2014-03-14 | 2015-09-17 | Solvay Sa | Multi-well solution mining exploitation of an evaporite mineral stratum |
US9879516B2 (en) * | 2014-03-14 | 2018-01-30 | Solvay Sa | Multi-well solution mining exploitation of an evaporite mineral stratum |
US10508528B2 (en) | 2014-03-14 | 2019-12-17 | Solvay Sa | Multi-well solution mining exploitation of an evaporite mineral stratum |
DE102021126656B3 (en) | 2021-10-14 | 2023-03-30 | Technische Universität Bergakademie Freiberg, Körperschaft des öffentlichen Rechts | Process for leaching metal-bearing ores using microorganisms |
Also Published As
Publication number | Publication date |
---|---|
AU7321374A (en) | 1976-03-18 |
ZA745723B (en) | 1975-10-29 |
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