US3148000A - Solution mining of potassium chloride - Google Patents
Solution mining of potassium chloride Download PDFInfo
- Publication number
- US3148000A US3148000A US176271A US17627162A US3148000A US 3148000 A US3148000 A US 3148000A US 176271 A US176271 A US 176271A US 17627162 A US17627162 A US 17627162A US 3148000 A US3148000 A US 3148000A
- Authority
- US
- United States
- Prior art keywords
- cavity
- potassium chloride
- water
- kcl
- roof
- 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
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 title claims description 232
- 239000001103 potassium chloride Substances 0.000 title claims description 116
- 235000011164 potassium chloride Nutrition 0.000 title claims description 116
- 238000005065 mining Methods 0.000 title description 8
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 121
- 239000011780 sodium chloride Substances 0.000 claims description 59
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 52
- 239000000243 solution Substances 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 8
- 239000011591 potassium Substances 0.000 claims description 8
- 229910052700 potassium Inorganic materials 0.000 claims description 8
- 238000011084 recovery Methods 0.000 claims description 8
- 239000012267 brine Substances 0.000 description 27
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 27
- 238000000605 extraction Methods 0.000 description 26
- 239000010410 layer Substances 0.000 description 12
- 239000013078 crystal Substances 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 230000007423 decrease Effects 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 239000004927 clay Substances 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000004891 communication Methods 0.000 description 3
- 208000002925 dental caries Diseases 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 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 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 235000011132 calcium sulphate Nutrition 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- BUKHSQBUKZIMLB-UHFFFAOYSA-L potassium;sodium;dichloride Chemical compound [Na+].[Cl-].[Cl-].[K+] BUKHSQBUKZIMLB-UHFFFAOYSA-L 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000011027 product recovery Methods 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003809 water extraction Methods 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
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D3/00—Halides of sodium, potassium or alkali metals in general
- C01D3/04—Chlorides
- C01D3/08—Preparation by working up natural or industrial salt mixtures or siliceous minerals
Definitions
- This invention relates to a novel method of mining potassium chloride deposits.
- Potassium chloride usually occurs in mineral deposits closely associated with sodium chloride. In many cases, potassium chloride exists in admixture or in combination with sodium chloride in the form of potassium chloriderich strata. Often, potassium chloride-rich strata (containing 15 to 60 percent by weight of KCl based upon the total weight of KCl and NaCl in the strata) are disposed immediately above other strata lean as to potassium chloride, that is, containing less than 15 percent KCl by weight based upon the weight of NaCl and KCl contained therein, or which contain no substantial amount of potassium chloride but which are preponderantly sodium chloride. These mineral deposits usually contain other materials, generally clays and salts such as calcium sulphate, magnesium sulphate and the like in small quantities, typically, about 2 to 15 percent.
- Subterranean deposits of potassium chloride and sodium chloride of this type frequently are very deep. For example, Canadian deposits of this character are often found 3,000 feet or more below the surface of the ground.
- This invention provides an improved method of recovering potassium chloride from a natural deposit containing potassium chloride.
- a cavity is first established in the deposit by feeding water thereto.
- the cavity is increased in size by reducing the water pressure therein thereby causing its roof to collapse.
- a large surface area of potassium chloride-rich ore is provided within the cavity.
- the rate of recovery of potassium chloride from the cavity is substantially increased.
- the aforementioned difficulties are overcome by the process of this invention which involves sinking a cased bore hole through a potassium chloride-rich deposit (wherein the potassium chloride content is typically 5 to 60 percent, preferably 15 to 60 percent, based upon the weight of KCl and NaCl in the deposit) into a sodium chloride-rich deposit disposed below the KCl-rich deposit, typically containing less than 5 percent (though may range as high as 15 percent) by weight of KCl, basis weight of KCl and NaCl in the deposit.
- a cavity is established in the NaCl-rich deposit by extraction with Water. On proper adjustment of extraction, the cavity is enlarged and its roof is raised to contact the potassium chloride-rich deposit.
- the water pressure in the cavity is then reduced to a pressure low enough to cause collapse of the cavitys roof, thereby depositing a portion of the KCl-rich strata to the floor of the cavity in the form of particles.
- Water extraction of the salts in the cavity is continued to remove KCl from the facing of the cavity and the particulate salt portion distributed on the floor of the cavity.
- a bore hole is drilled through the potassium chloride-rich strata or deposit and downwardly into the zone in which the potassium chloride concentration is low, i.e., below 15 percent based upon the weight of KCl and NaCl, or is substantially nonexistent and where the sodium chloride is comparatively high.
- water or an aqueous solution which is unsaturated as to sodium chloride is caused to flow down the cased hole either through a pipe disposed in the well or through the concentric area within the hole but outside the pipe, and sodium chloride is extracted from the potassium chloride-lean, sodium chloride-rich strata to establish a cavity in the manner well-known to the art of extracting sodium chloride from subterranean deposits.
- a waterimmiscible inert fiuid which may be air, nitrogen or like inert gas, but preferably a liquid which has a density lower than that of water at the temperature of operation, such as mineral oil, crude or refined petroleum oil, or like hydrocarbon oil, is fed into the cavity in order to establish a thin layer at the roof thereof.
- a waterimmiscible inert fiuid which may be air, nitrogen or like inert gas, but preferably a liquid which has a density lower than that of water at the temperature of operation, such as mineral oil, crude or refined petroleum oil, or like hydrocarbon oil
- the significance of the process of this invention resides in providing in the cavity a surface area of potassium chloride-rich ore which heretofore was unavailable for extraction purposes. This allows for considerable latitude in the mode of extraction. For example, potassium chloride may be more selectively extracted as opposed to the extraction of a mixture of NaCl and KCl in the proportion in which they occur in the deposit. As a result, the cost of recovery of KCl is substantially reduced.
- the process of this invention averts this difficulty by providing a large enough surface area that regardless of the amount of NaCl crystal accumulation on the particles or wall of the cavity, reasonable rates of KCl recovery are obtainable. Furthermore, if and when NaCl crystal formation does impair productivity, the roof of the cavity may again be collapsed thereby providing suflicient and productive surface are in the cavity.
- the NaCl content of the aqueous solution is in excess of 50 percent by weight of the NaCl content of a corresponding saturated solution.
- partial or fully saturated sodium chloride solution it is possible to selectively extract potassium chloride to the significant exclusion of NaCl.
- the necessity of separating NaCl from the cavity brine during the product recovery steps is substantially removed (typically eliminated). This reduces the high cost attendant with evaporting procedures conventionally employed for separating NaCl from KCl.
- roof collapsing causes rapid expansion of the cavity. This makes available greater cavity wall surface area for extraction of KCl. As a result, larger quantities of extractant may be fed to the cavity thereby increasing productivity of the mining operation.
- this increased surface area available for extraction means that reasonable rates of KCl recovery are obtainable from deposits extremely low in KCl content.
- the process of this invention increases the potentials of KCl mineral deposits heretofore considered undesirable.
- water pressure in the cavity typically ranges from 0.4 to 1 pound per square inch, preferably from .42 to .52 pound per square inch, per foot of depth from ground surface to the base of the cavity.
- the roof of the cavity will totally or partially collapse.
- water pressure is reduced by 50 percent or more.
- the effect of roof collapse is noted by the increased salt concentration, particularly KCl concentration, in the brine received from the well.
- Decrease of water or brine pressure in the cavity can be achieved by reducing or discontinuing water flow to the cavity and increasing the withdrawal rate of brine from the cavity through an outgoing hole.
- Collapsing of the cavity is generally effected when the roof of the cavity is at the base of the potassium chloride-rich strata. It is possible, on the other hand, to cause collapse of the cavity when the roof thereof is, e.g., within feet of the potassium chloride-rich strata.
- the lower sodium chloride-rich strata is separated from the potassium chloride-rich strata by a layer of clay. It is possible, under these circumsances, to develop the cavity in the sodium chloride-rich strata to achieve contact with this clay layer, that is, the clay lever forms the roof of the cavity. At this point, the water pressure within the cavity is reduced and the layer of clay is collapsed to allow for immediate contact with the potassium chloride-rich strata. Further collapse of the cavitys roof upon contact with the potassium chloride-rich strata is then possible.
- Control of the collapsing of the roof of the cavity can be achieved by employing the maximum water pressure in the cavity capable of allowing roof collapse. In this way it is possible to maintain a more regulated feed of particulate KCl-rich mineral to the floor of the cavity. As a rule, it is best to stage the roof collapsing at a rate equivalent to the maximum KCl concentration recoverable from the cavity.
- FIGURE 1 shows a typical cavity being developed below the mineable deposit.
- FIGURE 2 shows a preferred embodiment with two cased bore holes communicating with a subterranean cavity.
- a bore hole suitably fitted with a casing 1 is drilled through the bed rock into the subterranean deposit, through the potassium chloride-rich layer and and into the potassium chloride-lean, sodium chloride-rich layer.
- the potassium chloride-rich layer may have the following approximate composition:
- KCl Percent by weight KCl 15 to 40. Water insoluble clay About 1 toS. Calcium sulfate 1 to 5.
- the potassium chloride-lean or sodium chloride-rich deposit may have the following typical composition:
- a pipe 2 concentrically within the casing 1 of the hole. Water is then caused to flow down the hole in order to extract sodium chloride from the deposit.
- the water is allowed to flow downwardly in the space between the pipe and the casing and substantially saturated sodium chloride is withdrawn from the lower part of the cavity as it is formed via pipe 2.
- An immiscible fluid which has a density lower than that of water and which is insoluble in or immiscible with water (preferably hydrocarbon oil) is fed in small amounts (usually in amount up to about 10 pounds of such agent per cubic foot of salt withdrawn) into the hole along with the water. As a consequence, this fluid forms a protective layer 6 at the upper portion of the cavity 8 which is produced.
- the amount of such fluid which is introduced should be enough to establish a layer of /2 to 8 inches at the top of the cavity in order to protect the roof thereof. This amount can be computed roughly by estimating the approximate volume of the cavity from the number of tons of sodium chloride which is extracted from the cavity. Usually, about 0.1 to 2 pounds of hydrocarbon oil is fed per cubic foot of salts withdrawn.
- the water pressure or brine pressure within the cavity can be reduced to the aforementioned values causing a collapse of the cavitys roof.
- the KCl extraction is conducted while controlling the level of the cavity roof so that it rises at a very gradual rate or at a rapid rate through roof collapse of the KC1-rich deposit in the manner described above.
- FIGURE 2 it is desired to effect extraction of potassium chloride through a pair of cased bore holes.
- it is more desirable to conduct the extraction by feeding water or a partially unsaturated aqueous solution down one hole and withdrawing the resulting KCl-sodium chloride brine from the brine pool from another hole.
- FIGURE 2 two holes, 11 and 21, are drilled and developed substantially, as has been described above, by establishing cavities in the sodium chloride-rich deposit. Extraction of the sodium chloride solution from the sodium chloride-rich deposit is accomplished from one or from both of the holes until the cavity 3 has been caused to expand laterally to the point where it is in communication with both holes.
- a cavity 8 as is diagrammatically shown in FIGURE 2.
- This cavity has a thin layer of the inert, immiscible fluid 6 comparable in character to the layer discussed in connection with FIGURE 1.
- roof collapse can be achieved by reducing the Water or brine pressure in the cavity, e.g,, by adjustment of the water head in the incoming hole 11 and outgoing hole 21.
- the water pressure is increased through hole 11 and potassium chloridesodium chloride solution is withdrawn from hole 21, usually from a level below that at which water is introduced through hole 11 and often at or near the bottom of the cavity but above the level where crystals or insoluble impurities have accumulated to an appreciable degree.
- a solution of sodium chloride and potassium chloride which is unsaturated as to both sodium chloride and potassium chloride, may be fed down the hole.
- Potassium chloride absorbs heat when it is dissolved in water. To compensate for this, it is desirable that the temperature of the Water or sodium chloride-potassium chloride solution fed down hole 11 be at least to 100 F. higher than the temperature of the potassium chloride brine coming from hole 21. By this means, heated solution is supplied to the pool of brine in the cavity 8 and thus undue cooling of this cavity is prevented.
- one significant feature of this invention lies in its adaptability for the selective extraction of potassium chloride while leaving the essential sodium chloride content of the deposit remaining in the cavity.
- the extractant partially or totally saturated sodium chloride solution, typically an aqueous solution containing sodium chloride in amounts of from 50 percent by weight of total saturation up to total saturation.
- the brine solution employed for extraction may have a temperature ranging from up to 300 F. As the temperature of the brine solution is increased, likewise is the extraction rate of potassium chloride.
- the cavity used to commence dissolution of the potassium chloride may be formed by means other than extraction.
- a cavity may be excavated or formed by fracturing in the lower sodium chloride-rich layer or stratum or in the lower portion of the potassium chloride-rich stratum and then the roof of the cavity gradually raised to the potassium chloride-rich stratum by extraction and collapsing of the cavity roof as described above.
- More than two cased holes may be installed in communication with a single cavity and operated as contemplated herein.
- the improvement which comprises increasing the rate of recovery of potassium chloride from the cavity by alternately reducing the Water pressure in the cavity sufficiently to cause collapse, within said water-soluble stratum, of the cavity roof thereby increasing the surface area of potassium chloride being contacted by the water and increasing the water pressure within the cavity to prevent further collapse of the cavity roof until there is obtained a maximum concentration of potassium chloride in the brine removed from the cavity, feeding Water at increased pressure to extract potassium chloride until the concentration of potassium chloride in the brine decreases to approach the concentration of potassium chloride in the brine obtained prior to roof collapse and then again feeding water to the cavity alternately at reduced and increased pressure until there is obtained a maximum concentration of potassium chloride in the brine removed from the cavity.
- the improvement which comprises increasing '2 the rate of recovery of potassium chloride from the cavity by alternately reducing the water pressure in the cavity sufliciently to cause collapse of the cavity roof and increasing the water pressure within the cavity to prevent further collapse of the cavity roof until there is obtained a substantially increased concentration of potassium chloride in the brine removed from the cavity, and then feeding Water into the cavity at increased pressure to extract potassium chloride to obtain a. substantially increased concentration of potassium chloride in the brine removed from the cavity.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- Organic Chemistry (AREA)
- Geochemistry & Mineralogy (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Mining & Mineral Resources (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- Extraction Or Liquid Replacement (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
- Drilling And Exploitation, And Mining Machines And Methods (AREA)
Description
Sept. 8, 1964 J. B. DAHMS ETAL SOLUTION MINING 0F POTASSIUM CHLORIDE Filed Feb. 28, 1962 .zmomua z S 245 1 w s mi j VAM man n 8 M W 8 m tmofin .cmomua :us. 8 2m 5.2m .N H duh- 3 zoEjow u 5.2? 5:38 53 0 E ATTOkN'Y United States Patent SOLUTEON MINING OF POTASSIUM CHLORIDE James Bowen Dahms, Corpus Christi, and Byron P.
Edmonds, Alice, Tex., assignors to Pittsburgh Plate Glass Company, Pittsburgh, Pa., a corporation of Pennsylvania Filed Feb. 28, 1962, Ser. No. 176,271 2 Claims. (Cl. 299-5) This invention relates to a novel method of mining potassium chloride deposits.
Potassium chloride usually occurs in mineral deposits closely associated with sodium chloride. In many cases, potassium chloride exists in admixture or in combination with sodium chloride in the form of potassium chloriderich strata. Often, potassium chloride-rich strata (containing 15 to 60 percent by weight of KCl based upon the total weight of KCl and NaCl in the strata) are disposed immediately above other strata lean as to potassium chloride, that is, containing less than 15 percent KCl by weight based upon the weight of NaCl and KCl contained therein, or which contain no substantial amount of potassium chloride but which are preponderantly sodium chloride. These mineral deposits usually contain other materials, generally clays and salts such as calcium sulphate, magnesium sulphate and the like in small quantities, typically, about 2 to 15 percent.
Subterranean deposits of potassium chloride and sodium chloride of this type frequently are very deep. For example, Canadian deposits of this character are often found 3,000 feet or more below the surface of the ground.
Although some KCl has been produced from natural brines or from sodium chloride brines, as a practical matter substantially all of the potassium chloride recovered from underground is obtained by shaft, room and pillar type of mining in which the potassium chloridecontaining mineral is removed in solid state from the deposit and carried to the surface where it is treated by special techniques to separate potassium chloride.
Heretofore, recovery of potassium chloride by extract-- ing deposits of potassium chloride from subterranean resources with water has not been of commercial importance. Various problems are encountered in establishing a proper cavity suitable for the extraction of KCl. In addition, crystal formation of sodium chloride on the cavity wall seriously hampers extraction of KCl.
This invention provides an improved method of recovering potassium chloride from a natural deposit containing potassium chloride. According to this invention, a cavity is first established in the deposit by feeding water thereto. The cavity is increased in size by reducing the water pressure therein thereby causing its roof to collapse. In this fashion, a large surface area of potassium chloride-rich ore is provided within the cavity. Thus, the rate of recovery of potassium chloride from the cavity is substantially increased.
It is herein provided a process for the mining of potassium chloride from a subterranean deposit regardless of its content therein. Thus, it is now possible to remove KCl in effective and commercial amounts even though it is present in the deposit in amounts of from .1 to 15 percent or more, basis combined weight of sodium chloride and potassium chloride contained within said deposit.
The aforementioned difficulties are overcome by the process of this invention which involves sinking a cased bore hole through a potassium chloride-rich deposit (wherein the potassium chloride content is typically 5 to 60 percent, preferably 15 to 60 percent, based upon the weight of KCl and NaCl in the deposit) into a sodium chloride-rich deposit disposed below the KCl-rich deposit, typically containing less than 5 percent (though may range as high as 15 percent) by weight of KCl, basis weight of KCl and NaCl in the deposit. A cavity is established in the NaCl-rich deposit by extraction with Water. On proper adjustment of extraction, the cavity is enlarged and its roof is raised to contact the potassium chloride-rich deposit. The water pressure in the cavity is then reduced to a pressure low enough to cause collapse of the cavitys roof, thereby depositing a portion of the KCl-rich strata to the floor of the cavity in the form of particles. Water extraction of the salts in the cavity is continued to remove KCl from the facing of the cavity and the particulate salt portion distributed on the floor of the cavity.
In the practice of this process, a bore hole is drilled through the potassium chloride-rich strata or deposit and downwardly into the zone in which the potassium chloride concentration is low, i.e., below 15 percent based upon the weight of KCl and NaCl, or is substantially nonexistent and where the sodium chloride is comparatively high. At this point, water or an aqueous solution which is unsaturated as to sodium chloride is caused to flow down the cased hole either through a pipe disposed in the well or through the concentric area within the hole but outside the pipe, and sodium chloride is extracted from the potassium chloride-lean, sodium chloride-rich strata to establish a cavity in the manner well-known to the art of extracting sodium chloride from subterranean deposits.
In order to cause the cavity to grow laterally, a waterimmiscible inert fiuid, which may be air, nitrogen or like inert gas, but preferably a liquid which has a density lower than that of water at the temperature of operation, such as mineral oil, crude or refined petroleum oil, or like hydrocarbon oil, is fed into the cavity in order to establish a thin layer at the roof thereof. This causes the cavity to expand laterally as water is fed thereto and the sodium chloride dissolved in aqueous sodium chloride solution withdrawn from the cavity.
' On development of the cavity in the sodium chloriderich strata located below the potassium chloride-rich deposit to a size of at least 100 feet in diameter and in contact or close to contact with the potassium chloriderich strata deposit, the water pressure in the cavity is reduced until roof collapse results. It will be readily appreciated by those skilled in the art that the required reduction in pressure to cause roof collapse depends upon the diameter of the cavity, the depth from ground surbrine) through the pores.
face to the cavity roof and the distribution of impurities within the ore comprising the immediate roof of the cavity. This reduction in pressure can readily be accomplished to whatever degree required by pumping fluid from a hole communicating with the cavity, thus reducing the height of the fluid within the hole. As a result, collapse of the roof is effected causing particles of the potassium chloride-rich strata to be deposited in the cavity.
The significance of the process of this invention resides in providing in the cavity a surface area of potassium chloride-rich ore which heretofore was unavailable for extraction purposes. This allows for considerable latitude in the mode of extraction. For example, potassium chloride may be more selectively extracted as opposed to the extraction of a mixture of NaCl and KCl in the proportion in which they occur in the deposit. As a result, the cost of recovery of KCl is substantially reduced.
Heretofore, selective solution mining of KCl has been impaired by the decrease in the rate of solution of KCl in the deposit. This decrease is caused by the accumulation of sodium chloride crystals in the pore spaces on the wall of the cavity which prevents reasonable flow rates of the selective extractant (typically saturated NaCl These pores are formed as a result of selective extraction where only the KCl is leached from the cavity wall thereby leaving a spongy facing of NaCl. There proceeds, throughout this spongy facing, constant dissolution and precipitation of NaCl so that in a short time, NaCl crystals plug up the pores.
The process of this invention averts this difficulty by providing a large enough surface area that regardless of the amount of NaCl crystal accumulation on the particles or wall of the cavity, reasonable rates of KCl recovery are obtainable. Furthermore, if and when NaCl crystal formation does impair productivity, the roof of the cavity may again be collapsed thereby providing suflicient and productive surface are in the cavity.
It is within the contemplation of this invention to employ water free of NaCl and/or KCl or water partially or fully saturated with sodium chloride for extracting KCl from the deposit. Preferably, the NaCl content of the aqueous solution is in excess of 50 percent by weight of the NaCl content of a corresponding saturated solution. When partial or fully saturated sodium chloride solution is employed, it is possible to selectively extract potassium chloride to the significant exclusion of NaCl. When such a selective extraction operation is employed, the necessity of separating NaCl from the cavity brine during the product recovery steps is substantially removed (typically eliminated). This reduces the high cost attendant with evaporting procedures conventionally employed for separating NaCl from KCl.
In addition to providing increased product ore surface area in the cavity in the form of particles, roof collapsing causes rapid expansion of the cavity. This makes available greater cavity wall surface area for extraction of KCl. As a result, larger quantities of extractant may be fed to the cavity thereby increasing productivity of the mining operation.
Moreover, this increased surface area available for extraction means that reasonable rates of KCl recovery are obtainable from deposits extremely low in KCl content. The process of this invention increases the potentials of KCl mineral deposits heretofore considered undesirable.
During extraction of the salts from the cavity, water pressure in the cavity typically ranges from 0.4 to 1 pound per square inch, preferably from .42 to .52 pound per square inch, per foot of depth from ground surface to the base of the cavity. On reduction of the water pressure in the cavity up to partial or essentially complete removal of water or brine therefrom, the roof of the cavity will totally or partially collapse. Preferably, water pressure is reduced by 50 percent or more. The effect of roof collapse is noted by the increased salt concentration, particularly KCl concentration, in the brine received from the well.
Decrease of water or brine pressure in the cavity can be achieved by reducing or discontinuing water flow to the cavity and increasing the withdrawal rate of brine from the cavity through an outgoing hole.
Collapsing of the cavity is generally effected when the roof of the cavity is at the base of the potassium chloride-rich strata. It is possible, on the other hand, to cause collapse of the cavity when the roof thereof is, e.g., within feet of the potassium chloride-rich strata.
On many occasions, the lower sodium chloride-rich strata is separated from the potassium chloride-rich strata by a layer of clay. It is possible, under these circumsances, to develop the cavity in the sodium chloride-rich strata to achieve contact with this clay layer, that is, the clay lever forms the roof of the cavity. At this point, the water pressure within the cavity is reduced and the layer of clay is collapsed to allow for immediate contact with the potassium chloride-rich strata. Further collapse of the cavitys roof upon contact with the potassium chloride-rich strata is then possible.
Control of the collapsing of the roof of the cavity can be achieved by employing the maximum water pressure in the cavity capable of allowing roof collapse. In this way it is possible to maintain a more regulated feed of particulate KCl-rich mineral to the floor of the cavity. As a rule, it is best to stage the roof collapsing at a rate equivalent to the maximum KCl concentration recoverable from the cavity.
Thus, it is possible to deposit only a small particulate portion of the KCl-rich strata to the floor of the cavity. On further extraction of the cavity on increasing water pressure in the cavity, an increase in the KCl concentration of the brine withdrawn from the cavity will be noted. Repeated water pressure reductions, each followed by increase in water pressure, may be effected until there is obtained a maximum concentration of KCl in the brine obtained from the well. Extraction should then be continued to the point where a slight decrease in the KCl concentration is noted in the brine during the run. This decreased KCl concentration should be less than the highest KCl concentration of the brine after collapse but more than the KCl concentration of the brine normally obtained from the cavity prior to collapse of the cavity roof. Once such a decrease is noted, the pressure is maintained at normal extraction values to prevent further roof collapse within the cavity until the KCl concentration in the brine begins to show a value approaching that of brine obtained prior to roof collapse.
This process is diagrammatically illustrated in the accompanying drawings. FIGURE 1 shows a typical cavity being developed below the mineable deposit. FIGURE 2 shows a preferred embodiment with two cased bore holes communicating with a subterranean cavity. As shown in FIGURE 1, a bore hole suitably fitted with a casing 1 is drilled through the bed rock into the subterranean deposit, through the potassium chloride-rich layer and and into the potassium chloride-lean, sodium chloride-rich layer. The potassium chloride-rich layer may have the following approximate composition:
Percent by weight KCl 15 to 40. Water insoluble clay About 1 toS. Calcium sulfate 1 to 5.
Water soluble calcium and magnesium salts,
such as MgCl MgSO and Ca(HCO About 2. NaCl Remainder.
The potassium chloride-lean or sodium chloride-rich deposit may have the following typical composition:
Percent by weight There is then disposed a pipe 2 concentrically within the casing 1 of the hole. Water is then caused to flow down the hole in order to extract sodium chloride from the deposit. In the embodiment, as illustrated, the water is allowed to flow downwardly in the space between the pipe and the casing and substantially saturated sodium chloride is withdrawn from the lower part of the cavity as it is formed via pipe 2. An immiscible fluid which has a density lower than that of water and which is insoluble in or immiscible with water (preferably hydrocarbon oil) is fed in small amounts (usually in amount up to about 10 pounds of such agent per cubic foot of salt withdrawn) into the hole along with the water. As a consequence, this fluid forms a protective layer 6 at the upper portion of the cavity 8 which is produced.
The amount of such fluid which is introduced should be enough to establish a layer of /2 to 8 inches at the top of the cavity in order to protect the roof thereof. This amount can be computed roughly by estimating the approximate volume of the cavity from the number of tons of sodium chloride which is extracted from the cavity. Usually, about 0.1 to 2 pounds of hydrocarbon oil is fed per cubic foot of salts withdrawn.
In general, it is not necessary to drill into the sodium chloride-rich layer to any great depth. Usually extraction of sodium chloride from the sodium chloriderich deposit is conducted at a level of l to 50 feet below the level of the potassium chloride rich deposit which it is ultimately desired to extract.
As a consequence of the operation, water is caused to flow rapidly into the hole and a solution of sodium chloride withdrawn therefrom, and the cavity enlarges laterally to a substantial size, for example, preferably 100 feet or more in diameter, while the roof of the cavity is in contact or close to contact with the KCl-rich deposit.
It is at this point that the water pressure or brine pressure within the cavity can be reduced to the aforementioned values causing a collapse of the cavitys roof. Thereafter the KCl extraction is conducted while controlling the level of the cavity roof so that it rises at a very gradual rate or at a rapid rate through roof collapse of the KC1-rich deposit in the manner described above.
According to a preferred embodiment of the invention, it is desired to effect extraction of potassium chloride through a pair of cased bore holes. Thus, it is more desirable to conduct the extraction by feeding water or a partially unsaturated aqueous solution down one hole and withdrawing the resulting KCl-sodium chloride brine from the brine pool from another hole. This is accomplished as diagrammatically illustrated in FIGURE 2. As shown therein, two holes, 11 and 21, are drilled and developed substantially, as has been described above, by establishing cavities in the sodium chloride-rich deposit. Extraction of the sodium chloride solution from the sodium chloride-rich deposit is accomplished from one or from both of the holes until the cavity 3 has been caused to expand laterally to the point where it is in communication with both holes. There is then established a cavity 8, as is diagrammatically shown in FIGURE 2. This cavity has a thin layer of the inert, immiscible fluid 6 comparable in character to the layer discussed in connection with FIGURE 1.
When the holes are in communication and have been raised to a point where the roof of the cavity is in contact with the bottom of the KCl-n'ch deposit, roof collapse can be achieved by reducing the Water or brine pressure in the cavity, e.g,, by adjustment of the water head in the incoming hole 11 and outgoing hole 21. After the roof the cavity is collapsed, the water pressure is increased through hole 11 and potassium chloridesodium chloride solution is withdrawn from hole 21, usually from a level below that at which water is introduced through hole 11 and often at or near the bottom of the cavity but above the level where crystals or insoluble impurities have accumulated to an appreciable degree. Alternatively, a solution of sodium chloride and potassium chloride, which is unsaturated as to both sodium chloride and potassium chloride, may be fed down the hole.
Potassium chloride absorbs heat when it is dissolved in water. To compensate for this, it is desirable that the temperature of the Water or sodium chloride-potassium chloride solution fed down hole 11 be at least to 100 F. higher than the temperature of the potassium chloride brine coming from hole 21. By this means, heated solution is supplied to the pool of brine in the cavity 8 and thus undue cooling of this cavity is prevented.
As stated previously, one significant feature of this invention lies in its adaptability for the selective extraction of potassium chloride while leaving the essential sodium chloride content of the deposit remaining in the cavity. Thus, it is possible to employ, as the extractant, partially or totally saturated sodium chloride solution, typically an aqueous solution containing sodium chloride in amounts of from 50 percent by weight of total saturation up to total saturation. Advantageously, the brine solution employed for extraction, that is, the aqueous sodium chloride solution, may have a temperature ranging from up to 300 F. As the temperature of the brine solution is increased, likewise is the extraction rate of potassium chloride.
It has been found that by providing a large surface area within the cavity by the deposition of particulate ores therein, the amount of extraction achieved through the selective method is equivalent to the best yields obtainable under other conditions yet is achieved without the deleterious effects from sodium chloride crystal formation over the facing of the deposit within said cavity and which normally would preclude the utilization of brine solution as an extractant.
In operation of this process, it is advisable to provide after collapse that the incoming or outgoing hole located near the zone of collapse terminates at the base of the cavity. This is particularly desirable in the case of the incoming hole which, as a rule, will be closer to the zone of collapse than the outgoing hole. If as a result of roof collapse the incoming hole is damaged then a new tubing can be inserted therein and driven close to the base of the cavity by known drilling techniques.
It will be understood that the process herein contemplated is subject to numerous variations. For example, the cavity used to commence dissolution of the potassium chloride may be formed by means other than extraction. Thus, a cavity may be excavated or formed by fracturing in the lower sodium chloride-rich layer or stratum or in the lower portion of the potassium chloride-rich stratum and then the roof of the cavity gradually raised to the potassium chloride-rich stratum by extraction and collapsing of the cavity roof as described above.
More than two cased holes may be installed in communication with a single cavity and operated as contemplated herein.
Although the present invention has been described with reference to specific details of certain embodiments thereof, it is not intended that such details should be regarded as limitations upon the scope of the invention, except insofar as included in the accompanying claims.
We claim:
1. In the method of recovering potassium chloride from a water-soluble subterranean stratum containing potassium chloride and sodium chloride by establishing a cavity in the stratum and feeding water to the cavity to dissolve potassium chloride from the stratum thereby forming a potassium chloride enriched solution which is withdrawn from the cavity, the improvement which comprises increasing the rate of recovery of potassium chloride from the cavity by alternately reducing the Water pressure in the cavity sufficiently to cause collapse, within said water-soluble stratum, of the cavity roof thereby increasing the surface area of potassium chloride being contacted by the water and increasing the water pressure within the cavity to prevent further collapse of the cavity roof until there is obtained a maximum concentration of potassium chloride in the brine removed from the cavity, feeding Water at increased pressure to extract potassium chloride until the concentration of potassium chloride in the brine decreases to approach the concentration of potassium chloride in the brine obtained prior to roof collapse and then again feeding water to the cavity alternately at reduced and increased pressure until there is obtained a maximum concentration of potassium chloride in the brine removed from the cavity.
2. In the method of recovering potassium chloride from a water-soluble subterranean stratum containing potassium chloride and sodium chloride by establishing a cavity in the stratum and feeding water to the cavity to dissolve potassium chloride from the stratum thereby forming a potassium chloride-rich solution which is withdrawn from the cavity, the improvement which comprises increasing '2 the rate of recovery of potassium chloride from the cavity by alternately reducing the water pressure in the cavity sufliciently to cause collapse of the cavity roof and increasing the water pressure within the cavity to prevent further collapse of the cavity roof until there is obtained a substantially increased concentration of potassium chloride in the brine removed from the cavity, and then feeding Water into the cavity at increased pressure to extract potassium chloride to obtain a. substantially increased concentration of potassium chloride in the brine removed from the cavity.
References Cited in the file of this patent UNITED STATES PATENTS Tracy May 29, 1934 Cross June 13, 1939 Pullen Aug. 12, 1958 Rule Jan. 5, 1960 Bays Apr. 11, 1961
Claims (1)
- 2. IN THE METHOD OF RECOVERING POTASSIUM CHLORIDE FROM A WATER-SOLUBLE SUBTERRANEAN STRATUM CONTAINING POTASSIUM CHLORIDE AND SODIUM CHLORIDE BY ESTABLISHING A CAVITY IN THE STRATUM AND FEEDING WATER TO THE CAVITY TO DISSOLVE POTASSIUM CHLORIDE FROM THE STRATUM THEREBY FORMING A POTASSIUM CHLORIDE-RICH SOLUTION WHICH IS WITHDRAWN FROM THE CAVITY, THE IMPROVEMENT WHICH COMPRISES INCREASING THE RATE OF RECOVERY OF POTASSIUM CHLORIDE FROM THE CAVITY BY ALTERNATELY REDUCING THE WATER PRESSURE IN THE CAVITY SUFFICIENTLY TO CAUSE COLLAPSE OF THE CAVITY ROOF AND INCREASING THE WATER PRESSURE WITHIN THE CAVITY TO PREVENT FURTHER COLLAPSE OF THE CAVITY FOOR UNTIL THERE IS OBTAINED A SUBSTANTIALLY INCREASED CONCENTRATION OF POTASSIUM CHLORIDE IN THE BRINE REMOVED FROM THE CAVITY, AND THEN FEEDING WATER INTO THE CAVITY AT INCREASED PRESSURE TO EXTRACT POTASSIUM CHLORIDE TO OBTAIN A SUBSTANTIALLY INCREASED CONCENTRATION OF POTASSIUM CHLORIDE IN THE BRINE REMOVED FROM THE CAVITY.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US176271A US3148000A (en) | 1962-02-28 | 1962-02-28 | Solution mining of potassium chloride |
| ES284853A ES284853A1 (en) | 1962-02-28 | 1963-02-05 | A method for recovering potassium chloride from a natural deposit containing sodium and potassic chloride (Machine-translation by Google Translate, not legally binding) |
| DEP31091A DE1229941B (en) | 1962-02-28 | 1963-02-06 | Process for the extraction of potassium chloride from natural deposits containing KCl and NaCl |
| GB5106/63A GB962527A (en) | 1962-02-28 | 1963-02-07 | Recovery of potassium chloride from natural deposits |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US176271A US3148000A (en) | 1962-02-28 | 1962-02-28 | Solution mining of potassium chloride |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3148000A true US3148000A (en) | 1964-09-08 |
Family
ID=22643688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US176271A Expired - Lifetime US3148000A (en) | 1962-02-28 | 1962-02-28 | Solution mining of potassium chloride |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US3148000A (en) |
| DE (1) | DE1229941B (en) |
| ES (1) | ES284853A1 (en) |
| GB (1) | GB962527A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3278234A (en) * | 1965-05-17 | 1966-10-11 | Pittsburgh Plate Glass Co | Solution mining of potassium chloride |
| US3574402A (en) * | 1969-03-18 | 1971-04-13 | Continental Oil Co | Fracture initiation by dissolving a soluble formation |
| US4192555A (en) * | 1978-08-22 | 1980-03-11 | Ppg Industries Canada Ltd. | Method of disposing solid sodium chloride while selectively solution mining potassium chloride |
| DE3002757A1 (en) * | 1979-02-01 | 1980-08-14 | Ppg Ind Canada Ltd | SOLUTION OF POTASSIUM CHLORIDE FROM A WARMED UNDERGROUND CAVITY |
| US4232902A (en) * | 1979-02-09 | 1980-11-11 | Ppg Industries, Inc. | Solution mining water soluble salts at high temperatures |
| US4264104A (en) * | 1979-07-16 | 1981-04-28 | Ppg Industries Canada Ltd. | Rubble mining |
| US4367985A (en) * | 1978-10-17 | 1983-01-11 | Uniwersytet Mikolaja Kopernika | Method of sealing salina excavations |
| RU2236577C1 (en) * | 2003-05-05 | 2004-09-20 | Санкт-Петербургский государственный горный институт им. Г.В. Плеханова (Технический университет) | Method for extracting salts from salt deposits |
| US9365349B1 (en) | 2015-11-17 | 2016-06-14 | Air Liquide Large Industries U.S. Lp | Use of multiple storage caverns for product impurity control |
| US9399810B2 (en) | 2014-11-18 | 2016-07-26 | Air Liquide Large Industries U.S. Lp | Materials of construction for use in high pressure hydrogen storage in a salt cavern |
| US9482654B1 (en) | 2015-11-17 | 2016-11-01 | Air Liquide Large Industries U.S. Lp | Use of multiple storage caverns for product impurity control |
| US9573762B2 (en) | 2015-06-05 | 2017-02-21 | Air Liquide Large Industries U.S. Lp | Cavern pressure management |
| US9656807B2 (en) | 2014-05-08 | 2017-05-23 | Air Liquide Large Industries U.S. Lp | Hydrogen cavern pad gas management |
| CN109252852A (en) * | 2018-10-12 | 2019-01-22 | 中国科学院青海盐湖研究所 | The molten mining method of Quaternary Period Africa underground potassium mine |
| US11073008B2 (en) | 2018-05-29 | 2021-07-27 | Buffalo Potash Corp. | Horizontal line drive selective solution mining methods |
| US11634978B2 (en) | 2020-02-18 | 2023-04-25 | Canatech Management Services Inc. | Methods for recovering a mineral from a mineral-bearing deposit |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1296587B (en) * | 1966-05-24 | 1969-06-04 | Kalium Chemicals Ltd | Process for leaching mineral salts from underground layers |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1960932A (en) * | 1933-07-21 | 1934-05-29 | Solvay Process Co | Method of mining |
| US2161800A (en) * | 1937-04-10 | 1939-06-13 | Cross Roy | Mining potash |
| US2847202A (en) * | 1956-02-09 | 1958-08-12 | Fmc Corp | Method of mining salt using two wells connected by fluid fracturing |
| US2919909A (en) * | 1958-03-27 | 1960-01-05 | Fmc Corp | Controlled caving for solution mining methods |
| US2979317A (en) * | 1959-08-12 | 1961-04-11 | Fmc Corp | Solution mining of trona |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2772868A (en) * | 1954-01-18 | 1956-12-04 | Phillips Petroleum Co | Apparatus for control of roof location in the formation of underground caverns by solution mining |
| US2850270A (en) * | 1956-03-19 | 1958-09-02 | Alden W Hanson | Mining soluble minerals using passageway formed by fracturing |
-
1962
- 1962-02-28 US US176271A patent/US3148000A/en not_active Expired - Lifetime
-
1963
- 1963-02-05 ES ES284853A patent/ES284853A1/en not_active Expired
- 1963-02-06 DE DEP31091A patent/DE1229941B/en active Pending
- 1963-02-07 GB GB5106/63A patent/GB962527A/en not_active Expired
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1960932A (en) * | 1933-07-21 | 1934-05-29 | Solvay Process Co | Method of mining |
| US2161800A (en) * | 1937-04-10 | 1939-06-13 | Cross Roy | Mining potash |
| US2847202A (en) * | 1956-02-09 | 1958-08-12 | Fmc Corp | Method of mining salt using two wells connected by fluid fracturing |
| US2919909A (en) * | 1958-03-27 | 1960-01-05 | Fmc Corp | Controlled caving for solution mining methods |
| US2979317A (en) * | 1959-08-12 | 1961-04-11 | Fmc Corp | Solution mining of trona |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3278234A (en) * | 1965-05-17 | 1966-10-11 | Pittsburgh Plate Glass Co | Solution mining of potassium chloride |
| US3574402A (en) * | 1969-03-18 | 1971-04-13 | Continental Oil Co | Fracture initiation by dissolving a soluble formation |
| US4192555A (en) * | 1978-08-22 | 1980-03-11 | Ppg Industries Canada Ltd. | Method of disposing solid sodium chloride while selectively solution mining potassium chloride |
| US4367985A (en) * | 1978-10-17 | 1983-01-11 | Uniwersytet Mikolaja Kopernika | Method of sealing salina excavations |
| FR2448029A1 (en) * | 1979-02-01 | 1980-08-29 | Ppg Ind Canada Ltd | PROCESS FOR THE EXTRACTION OF POTASSIUM CHLORIDE IN SOLUTION FROM HEATED UNDERGROUND CAVITIES |
| US4239287A (en) * | 1979-02-01 | 1980-12-16 | Ppg Industries Canada, Ltd. | Solution mining potassium chloride from heated subterranean cavities |
| DE3002757A1 (en) * | 1979-02-01 | 1980-08-14 | Ppg Ind Canada Ltd | SOLUTION OF POTASSIUM CHLORIDE FROM A WARMED UNDERGROUND CAVITY |
| US4232902A (en) * | 1979-02-09 | 1980-11-11 | Ppg Industries, Inc. | Solution mining water soluble salts at high temperatures |
| US4264104A (en) * | 1979-07-16 | 1981-04-28 | Ppg Industries Canada Ltd. | Rubble mining |
| RU2236577C1 (en) * | 2003-05-05 | 2004-09-20 | Санкт-Петербургский государственный горный институт им. Г.В. Плеханова (Технический университет) | Method for extracting salts from salt deposits |
| US9656807B2 (en) | 2014-05-08 | 2017-05-23 | Air Liquide Large Industries U.S. Lp | Hydrogen cavern pad gas management |
| US9399810B2 (en) | 2014-11-18 | 2016-07-26 | Air Liquide Large Industries U.S. Lp | Materials of construction for use in high pressure hydrogen storage in a salt cavern |
| US9573762B2 (en) | 2015-06-05 | 2017-02-21 | Air Liquide Large Industries U.S. Lp | Cavern pressure management |
| US9482654B1 (en) | 2015-11-17 | 2016-11-01 | Air Liquide Large Industries U.S. Lp | Use of multiple storage caverns for product impurity control |
| US9365349B1 (en) | 2015-11-17 | 2016-06-14 | Air Liquide Large Industries U.S. Lp | Use of multiple storage caverns for product impurity control |
| US11073008B2 (en) | 2018-05-29 | 2021-07-27 | Buffalo Potash Corp. | Horizontal line drive selective solution mining methods |
| CN109252852A (en) * | 2018-10-12 | 2019-01-22 | 中国科学院青海盐湖研究所 | The molten mining method of Quaternary Period Africa underground potassium mine |
| US11634978B2 (en) | 2020-02-18 | 2023-04-25 | Canatech Management Services Inc. | Methods for recovering a mineral from a mineral-bearing deposit |
Also Published As
| Publication number | Publication date |
|---|---|
| ES284853A1 (en) | 1963-04-16 |
| DE1229941B (en) | 1966-12-08 |
| GB962527A (en) | 1964-07-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3148000A (en) | Solution mining of potassium chloride | |
| US3262741A (en) | Solution mining of potassium chloride | |
| US3271962A (en) | Mining process | |
| US1960932A (en) | Method of mining | |
| US3335797A (en) | Controlling fractures during well treatment | |
| US4192555A (en) | Method of disposing solid sodium chloride while selectively solution mining potassium chloride | |
| US3278234A (en) | Solution mining of potassium chloride | |
| US3366419A (en) | Process for solution mining kci deposits | |
| US3612608A (en) | Process to establish communication between wells in mineral formations | |
| US3439953A (en) | Apparatus for and method of mining a subterranean ore deposit | |
| US2280851A (en) | Method of well drilling | |
| US3096969A (en) | Recovery of potassium chloride | |
| US3917345A (en) | Well stimulation for solution mining | |
| Thomeer et al. | Increasing occurrence of abnormally high reservoir pressures in boreholes, and drilling problems resulting therefrom | |
| US4408664A (en) | Secondary oil recovery method | |
| US3433530A (en) | Method of solution mining potassium chloride | |
| CA1172559A (en) | Solution mining of an inclined structure | |
| US4264104A (en) | Rubble mining | |
| US4007964A (en) | Preferential solution mining process | |
| US3574402A (en) | Fracture initiation by dissolving a soluble formation | |
| US3428129A (en) | Vertical fracture control | |
| US3632171A (en) | Method of controlling growth of brine wells | |
| US3370887A (en) | Hole preparation for fracturing solution mining wells | |
| US3442553A (en) | Slurry mining of carnallite | |
| US4239287A (en) | Solution mining potassium chloride from heated subterranean cavities |