US2161800A - Mining potash - Google Patents
Mining potash Download PDFInfo
- Publication number
- US2161800A US2161800A US136178A US13617837A US2161800A US 2161800 A US2161800 A US 2161800A US 136178 A US136178 A US 136178A US 13617837 A US13617837 A US 13617837A US 2161800 A US2161800 A US 2161800A
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- United States
- Prior art keywords
- potash
- liquor
- salts
- water
- cavity
- Prior art date
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 title description 74
- 229940072033 potash Drugs 0.000 title description 46
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 title description 46
- 235000015320 potassium carbonate Nutrition 0.000 title description 46
- 238000005065 mining Methods 0.000 title description 11
- 235000002639 sodium chloride Nutrition 0.000 description 53
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- 239000011780 sodium chloride Substances 0.000 description 29
- 239000000243 solution Substances 0.000 description 23
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 22
- 150000003839 salts Chemical class 0.000 description 22
- 229910052500 inorganic mineral Inorganic materials 0.000 description 15
- 238000000034 method Methods 0.000 description 15
- 235000010755 mineral Nutrition 0.000 description 15
- 239000011707 mineral Substances 0.000 description 15
- 239000012267 brine Substances 0.000 description 14
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 14
- 239000001103 potassium chloride Substances 0.000 description 12
- 235000011164 potassium chloride Nutrition 0.000 description 11
- 238000001816 cooling Methods 0.000 description 10
- 239000012452 mother liquor Substances 0.000 description 10
- 238000001556 precipitation Methods 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- 239000007788 liquid Substances 0.000 description 6
- 239000007791 liquid phase Substances 0.000 description 6
- 238000003303 reheating Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000007790 solid phase 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 3
- 238000001704 evaporation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 150000003112 potassium compounds Chemical class 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 150000004694 iodide salts Chemical class 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- 238000007790 scraping Methods 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 238000009931 pascalization Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004326 stimulated echo acquisition mode for imaging Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000005406 washing Methods 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
- E21B43/281—Dissolving minerals other than hydrocarbons, e.g. by an alkaline or acid leaching agent using heat
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S422/00—Chemical apparatus and process disinfecting, deodorizing, preserving, or sterilizing
- Y10S422/902—Sodium chloride and potassium chloride dissolver
Definitions
- 'I'his invention or discovery relates to mining potash; and it comprises a method of winning potassium compounds from underground potash beds, which comprises establishing and main- 5 taining a body of cyclically circulating superheated saline liquor'unsaturated with respect to potash in contact with such beds forming a hotwalled cavity, withdrawing therefrom hot liquid containing potash salts in solution, releasing 1,0 pressure and lowering temperature on the withdrawn liquor to cause precipitation of potash salts, removing said salts, and replenishing the underground body of superheated liquor by reheating the motor liquor remaining after precipitation of the potash salts and forcing it back into the bed; all as more fully hereinafter set forth and as claimed.
- I provide a process capable of economically mining deep-lying potash deposits; deposits too deep for ordinarily mining methods and containing such refractory minerals as polyhalite.
- Superheated water kept in the liquid phase by heavy pressure, at temperatures up to 200 C. and above, attacks potash minerals even when they are of a type ordinarily considered insoluble (e. g. polyhalite).
- the rise ot solubility of most potash salts with temperature is' very rapid; much more so than with most other salts; sodium salts for example. Accordingly, the superheated water takes up a substantial proportion of potash salts, and less amounts of other salts.
- the circulating current gradually forms a cavity, the walls of which are at a high temperature, and becomes vsaturated with salts.
- thermal and chemical equilibria are established. Die cavity walls reach a constant, high temperature, and the dissolved saline content of the circulating liquor is in equilibrium with the undissolved minerals.
- the system is a closed system substantially in equilibrium.
- the circulating liquid body is saturated with salts and is at approximately constant 'temperature throughout. Instead of water, I sometimes use superheated NaCl or CaCl: brine in establishing circulation.
- the process involves establishment and maintenance of a dominant pool of superheatedsaline liquor illling the cavity and tending to come into thermal and chemical equilibrium with the minerals forming the cavity walls. Some of the pool liquor is continually withdrawn, to be cooled and relieved of some of its potash content, and the pool is continually being replenished, by
- Fig. 1 is a diagrammaticai view of my invention applied to a single well in a potash bed.
- Fig. 2 is a modified form of the invention shown in Fig. 1, showing how my invention may be applied to a plurality of wells when desired to run the potash solvent from one well to another.
- Fig. 3 is a second modification to the invention shown in Fig. 1 in which a. steam heater I3 is shown added to -the single well of Fig. 1, but which heater could be added to any, or all, wells of Fig. 2 as'desired.
- the system is shown applied to a typical potash field as encountered in the southwestern part of the United States, with beds I of various potash minerals which may be several hundred feet thick and lying at a depth of as much as 2000 to 3000 feet from the surface of the ground I I.
- 'I'he potash minerals occur as strata. of varying thickness separated by shale or the like indicated at I2.
- bed-rock I3 Underneath is bed-rock I3.
- a well is sunk substantially to the bed-rock horizon, as indicated in short-dashed lines at I4, and is cased oi as by a casing I 5 down as far as the potash deposit.
- a pipe I6 is sunk down through the casing with an outlet I 'I close to the bottom of the potash beds.
- the casing is closed at the top as at I3.
- iirst water or brine is injected into a heater or boiler by a pump 2
- Liquid flows up between the central pipe and vthe well bore, issuing from the top of the casing at 22 and is withdrawn through a pipe 23. In the begnning, this water is simply recirculated from pipe 23 to pipe I6 through a valved bypass 2l.
- 'I'he sprayl cooler is designed to bring the liquor to about weather temperature or below.
- 'I'he mother liquor contains some of the potash and all the dissolved 7 is forced by pump 2
- the cavity contains a body or pool of liquor, 32, which is at high temperature. It tends to come into chemical and thermal equilibria with the surrounding minerals. Portions of it are continually being withdrawn and unsaturated solution is continually being added to it, which tends to unbalance the equilibria.
- the rate of circulation is made-such that the liquor withdrawn is substantially saturated. Saturation takes some time. Ordinarily, a given unit quantity of circulating liquor will remain in the cavity at least one or two hours.
- the cavity becomes enlarged, say to the size indicated in long-dash lines at 33.
- the Superheated brine or Water is forced down one well and the concentrated liquor is withdrawn from the other well.
- Any desired number of wells can be used.
- Fig. 2 shows such an arrangement, heated mother liquor being forced down a central well 50 and saturated solution being withdrawn through output wells 5I and 52 spaced from the input well. Throttle valves 53 are provided', so that the flow from the output wells can be equalized.
- the output wells can be drilled directionaly (in a way known per se) so as to slant towards the bottom of the input well. It is convenient to provide four output Wells in a square, with the input well at the center.
- Fig. 2 shows the input Well and two of the output wells.
- the liquor coming up from the cavity is often more or less contaminated with mud, silt, sand, etc., and it is usually best to provide a closed settling chamber as indicated at 34, wherein the sludge may sette out of the hot liquor prior to passage t-o the spray cooler. Sludge may be removed through a sump outlet 35.
- a similar settler 36a is provided just before the spray cooler, as shown.
- make-up water or brine as required through an inlet 38 to the mother liquor prior to" going to the heat exchanger and hea-ter. Water can also be added at this point to make up for any dissipation in the underground bed. Make-up water can also be added to the liquor prior to the spray cooling if desired, a valved inlet 31 being provided as shown.
- the heater can be any suitable type of high pressure heater, and in the southwestern United States can conveniently be heated by natural gas, which occurs in regions adjacent the potash deposits.
- the heater, as well as the other ap# paratus elements which handle the circulating liquors, should be made of materials adapted to resist corrosion by the hot brines.
- the heater should be of a type adapted for easy cleaning, since some ofthe salines may deposit out from the liquors being heated, forming scale. Heaters constructed in a way similar to cracking stills, with detachable return bends giving access to the interior of the tubes for scraping, are useful.
- Fig. 3 1 have shown a modification of the invention in which the boiler is arranged to heat the liquor by indirect heat exchange, and which obviates scaling difliculties.
- the boiler is shown at 39.
- four concentric pipes are provided; the well 'casing I5, a pipe 40 for liquor. and two steam pipes 4I and 42.
- Pipes 4I and 42 may extend part way down the well, or clear to the bottom, as shown, and pipe 42 is capped at 43.
- high pressure steam is forced down and up the inner pipes, as indicated by the arrows, and liquor is circulated down pipe 40 and up between pipe 40 and the casing.
- the liquor is heated in its downward course.
- the boiler and steam tubes form a closed system and use plain water. Heat transfer media which give higher temperatures than water at the same pressure can be employed.
- the CO2 solution is and if it is desired to recover other compounds than potash, the heating and cooling temperay tures, and the degree of concentration of the liquor, are adjusted accordingly.
- Other saline deposits besides potash can be mined.
- bromides and iodides build up in the circulatingV liquor. From time to time, the liquor can be treated, for instance with chlorine and steam to displace the bromine and iodine; these subl'as stances being recovered in elemental form by fractional condensation.
- a method of winning potassium compounds from underground potash beds which comprises establishing and maintaining in contact with such beds, a body of superheated aqueous solution of a compound selected from the class consisting of sodium chloride and calcium chloride, the solution being unsaturated with respect to potash, thereby disolving potash and forming a hot-walled cavity, withdrawing liquor from said body containing potash in solution as chloride, cooling the withdrawn liquor to cause precipitation of potassium chloride therefrom, removing the precipitated potasium chloride, reheating to a superheated condition the mother liquor remaining after precipitation of the potash salts, and forcing it back into the cavity to replenish said body of liquor.
- a method of winning potash compounds from underground polyhalite beds which comprises establishing and maintaining a body of highly heated saline liquor in contact with such beds for an extended period of contact so as to dissolve potash and form a hot-walled cavity, withdrawing liquor fromv said body containing potash salts in solution, cooling the withdrawn -liquor to cause precipitation of potash salts therefrom, removing the precipitated salts, reheating the remaining mother liquor to a temperature of at least 200 C. under superatmospheric pressure and forcing it back into the cavity to replenish said body of liquor.
- a method of winning potassium compounds i from underground potash beds comprises establishing a body of super-heated saline 'liquor in ⁇ contact with such beds to form a hot-walled cavity and dissolve potash, withdrawing liquor from said body containing potash salts in solution, cooling the withdrawn liquor to cause precipitation of potash salts therefrom, removing said precipitated salts, and maintaining said body of liquor in super-heated condition in contact with the potash beds, by supplying heat thereto and replenishing it with dilute liquor.
- AV method of winning potash salts from potassium which comprises sending into contact 4 with such a deposit a bo'dy of superheated NaCl solution, removing and cooling the solution to crystallize out potassium chloride, reheating the solution to a superheated condition and returning the solution of NaCl in its super-heated state to the deposit for further attack thereon.
- a method of winning potash salts from subterranean deposits which comprises circulating downwardly into and through the deposits, superheated saline liquor unsaturated with respect to potash, at such rate as to provide an extended period of contact with a deposit, so as to take some of the potash therefrom, returning the hot solution upwardly, cooling the solution to a point sumcient to cause crystallization therefrom of at least some of the dissolved potash salts, reheating the solution to a superheated condition and-again returning it to extended contact with the deposits.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
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Description
2 Sheets-Sheet l NJN EGON @Hmm Qn mmm@ zwiwo foy Cross,
Imm
n I l lll Milling* R. cRoss MINING POTASH Filed April l0, 1937 QN WN June 13, 1939.
June 13, 1939. R. cRoss MINING POTASH Filed April lO, 1937 2 Sheets-Sheet 2 f77-Caf L3 I f STEAM q] q2 COOL LIQUOR FROM P ...SETTLING vm:
gmc/whom Jffoy Cross,
KRMCS,
. sylvinite Patented June 13, 1939 UNITED STATES PATENT oFF-TCE MINING POTASH Roy Cross, Kansas City, Mo.
Application April A10, 1937, Serial No. 136,178
Claims.
'I'his invention or discovery relates to mining potash; and it comprises a method of winning potassium compounds from underground potash beds, which comprises establishing and main- 5 taining a body of cyclically circulating superheated saline liquor'unsaturated with respect to potash in contact with such beds forming a hotwalled cavity, withdrawing therefrom hot liquid containing potash salts in solution, releasing 1,0 pressure and lowering temperature on the withdrawn liquor to cause precipitation of potash salts, removing said salts, and replenishing the underground body of superheated liquor by reheating the motor liquor remaining after precipitation of the potash salts and forcing it back into the bed; all as more fully hereinafter set forth and as claimed.
In western Texas and New Mexico there occur, over a wide area, subterranean beds of saline minerals, including potash salts. The beds are of varying thickness, are approximately horizontalvan'dcoccur at depths of 300 to 3000 feet or more.` .The potash occurs as the chloride in (KCl, NaCl) and, in much larger amounts, asa sulfate in polyhalite Many ofthe beds, however, contain indefinite .mixtures of complex salts containing potassium, calcium and-magnesium. In addition to chlorides and sulfates there are minor proportions of iodides, bromide'st and other substances. -The mineral beds often l,occuras thin streaks/or lay-` ers separated'by, sl 1ale..
vIn recoveringl'p'ot'ash iromthese deposits, most p attention has'` been'lpaid to syIVinite. This min'- eral can be vmined b'yf'methods-analogous'to those used in coal mining. and the'potash 'canbewon from the granulated mineralby. simple-solution? row as to beunprotableto mine in the dry way. It isv extremely old to recover salt (NaCl) from underground deposits through` wells by pumping out brine and replenishing the well cavity with water. In this operation the water is at ordinary temperature, the solubility of salt being about the same at all practical working temperatures. This simple procedure is equivalent to merely dissolving or Washing out the salt, and While attractive, it is not readily applicable to potassiferous salts for several reasons. For one thing potash contained in complex salts like polyhalite isattacked but slowly by water at any temperature.
According to the present invention I provide a process capable of economically mining deep-lying potash deposits; deposits too deep for ordinarily mining methods and containing such refractory minerals as polyhalite.
I have discovered' that underground beds of potash salts yield relatively rapidly to the action of hot water, particularly at a temperature of 200 C. or more, giving a saline liquor or brine rich in potash compounds. Even at C. substantial amounts of potash are brought into solution. A But I also iind that the action is one requiring time for the brine to come to any definite composition. In any cavity in a saline deposit it is a rare occurrence that there is a surface exposure of only one salt. 'I'his requirement for time to permit equilibration is particularly true with deposits including polyhalite. In attacking polyhalite by superheated water, there is a first solution of somecomponents, a liquid phase being produced not of the same composition Vas the solid phase. Rearrangement in the brine follows both as regards the liquid phase and the solid phase; new equilibria are established within the liquid phase and between the contacting liquid and solid phases. The composition of the brine changes. In some measure this is true in all `hot water extractions of potassiferous beds.
,-I. have further discovered that even better results can be obtained in some cases by attacking -thesubtrranean beds with a superheated solution of NaCl vor CaClz, in which case successive equilibria take place resulting in the building up of a'KCl concentration in the liquid phase at vthe expensev .of the solid phase. If the liquid be now removed from contact with the mineral, say polyhalite, and cooled to a temperature at which KCl crystallizes out, the KCl removed, and the mother liquor or brine reheated and sent back into renewed contact with polyhalite, the former equilibria once more recur; there is a preferential solution of KCl ,with some redeposition of NaCl. Sodium chloride, in typical brines produced under the invention, is even less-soluble at high temperatures .than at low temperatures.
According to the invention, I form a hot-walled cavity in the potash bed, by forcing into the bed, through a well, a superheated current of liquid, which at the beginning may be plain water, but becomes a saline solution. Superheated water, kept in the liquid phase by heavy pressure, at temperatures up to 200 C. and above, attacks potash minerals even when they are of a type ordinarily considered insoluble (e. g. polyhalite). The rise ot solubility of most potash salts with temperatureis' very rapid; much more so than with most other salts; sodium salts for example. Accordingly, the superheated water takes up a substantial proportion of potash salts, and less amounts of other salts. The circulating current gradually forms a cavity, the walls of which are at a high temperature, and becomes vsaturated with salts. In the course of time thermal and chemical equilibria are established. Die cavity walls reach a constant, high temperature, and the dissolved saline content of the circulating liquor is in equilibrium with the undissolved minerals. At this stage the system is a closed system substantially in equilibrium. The circulating liquid body is saturated with salts and is at approximately constant 'temperature throughout. Instead of water, I sometimes use superheated NaCl or CaCl: brine in establishing circulation.
I now break the circulation by releasing pressure and temperature on the liquor at the surface of the earth. I'hat is, the superheated liqk uor coming up through the wall is passed through a reducing valve or the like, and sprayed into the air. Upon this release of pressure, some of the water flashes into water vapor or steam, and droplets of cooled liquor fall into a pit or tank, forming a cool lake. Potash salts crystallize out at once, as their solubility is low at ordinary air temperatures, leaving a mother liquor retaining other salts in solution. Some of the potash salts remain dissolved, and almost all the other salts remain in solution since they are almost as soluble at air temperatures as at high temperatures. 'Ihe deposited potash salts are removed mechanically.
'I'he mother liquor remaining after deposition of the potash salts is now capable, upon being reheated, of dissolving more potash salts. It is now pumped under high pressure into a boiler and heated to a high temperature. I'he superheated liquoris forced down the well, into the cavity.` @The liquor is unsaturated with respect to potash salts but saturated as regards other salines. It is allowed to remain in contact with the cavity long enough. for potassium salts to be dissolved until equilibrium is again substantially attained, and the hot concentrated liquor is withdrawn and treated as before. l
The process involves establishment and maintenance of a dominant pool of superheatedsaline liquor illling the cavity and tending to come into thermal and chemical equilibrium with the minerals forming the cavity walls. Some of the pool liquor is continually withdrawn, to be cooled and relieved of some of its potash content, and the pool is continually being replenished, by
addition of superheated, mother liquor unsaturated as regards potassium salts. The pool liquor is continuously tending toward equilibrium with the saline beds, and the addition oi' heated unsaturated liquor continually tends to unbalance the equilibrium. 'I'he time factor is of considerable importance; it is better not to remove the brine as fast. as it forms without giving it time to stabilize. 'I'he dominant pool is oi.' magnitude suiilcient to allow withdrawals and replenishments to average out.
The higher the temperature the higher the ,yield. and I ordinarily heat the water to as .high a temperature as is conveniently practicable. Sometimes, as when the more soluble salts are being mined, I employ lower temperatures than those mentioned; temperatures as low as 100 This gives less yield, but saves on heating diagrammatically a mining system within the purview of the invention.
Fig. 1 is a diagrammaticai view of my invention applied to a single well in a potash bed.
Fig. 2 is a modified form of the invention shown in Fig. 1, showing how my invention may be applied to a plurality of wells when desired to run the potash solvent from one well to another.
Fig. 3 is a second modification to the invention shown in Fig. 1 in which a. steam heater I3 is shown added to -the single well of Fig. 1, but which heater could be added to any, or all, wells of Fig. 2 as'desired.
Referring to the drawings, the system is shown applied to a typical potash field as encountered in the southwestern part of the United States, with beds I of various potash minerals which may be several hundred feet thick and lying at a depth of as much as 2000 to 3000 feet from the surface of the ground I I. 'I'he potash minerals occur as strata. of varying thickness separated by shale or the like indicated at I2. Underneath is bed-rock I3. In the beginning, a well is sunk substantially to the bed-rock horizon, as indicated in short-dashed lines at I4, and is cased oi as by a casing I 5 down as far as the potash deposit. A pipe I6 is sunk down through the casing with an outlet I 'I close to the bottom of the potash beds. The casing is closed at the top as at I3. In beginning operations in the iield, iirst water or brine is injected into a heater or boiler by a pump 2|, is heated in the heater and is forced down the central pipe I6. Liquid flows up between the central pipe and vthe well bore, issuing from the top of the casing at 22 and is withdrawn through a pipe 23. In the begnning, this water is simply recirculated from pipe 23 to pipe I6 through a valved bypass 2l. In the course of time, the walls of the well cavity are heated and material is dissolved, thus beginning to Aform an enlarged cavity somewhat as indicated at 3I. Valved bypasses 8 and 9 between pipes I 6 and 23 allow the circulation to be reversed if desired. After a time thermal and chemical equilibria are established. I now begin recovering potash. Bypass 24 is closed and the hot concentrated liquor issuing from the well is passed through a reducing valve 25 to a spray cooler 26 arranged above a settling vat or pit 21. The liquor is thus cooled by evaporation and falls as droplets, forming a lake 28. Potash salts are deposited out and collect on the bottom as at 29, whence they are withdrawn by scraping means (not shown), and a conveyor 30. 'I'he sprayl cooler is designed to bring the liquor to about weather temperature or below. 'I'he mother liquor contains some of the potash and all the dissolved 7 is forced by pump 2| into the heater and reheated to temperatures of 200? C. or thereabouts and is then sent back into the well. The cavity contains a body or pool of liquor, 32, which is at high temperature. It tends to come into chemical and thermal equilibria with the surrounding minerals. Portions of it are continually being withdrawn and unsaturated solution is continually being added to it, which tends to unbalance the equilibria. The rate of circulation is made-such that the liquor withdrawn is substantially saturated. Saturation takes some time. Ordinarily, a given unit quantity of circulating liquor will remain in the cavity at least one or two hours.
It is sometimes desirable to force the heated mother liquor down between the casing and the central pipe, and withdraw the concentrated liquor through the central pipe. This has the advantage of obviating deposition of salts in the upper portion of the tubing. But the way rst described is usually better.
In the course of time the cavity becomes enlarged, say to the size indicated in long-dash lines at 33. When the cavity becomes quite large, I sometimes find it convenient to sink another well spaced from the original well, so as to have a lateral circulation. In this case, the Superheated brine or Water is forced down one well and the concentrated liquor is withdrawn from the other well. Any desired number of wells can be used. Fig. 2 shows such an arrangement, heated mother liquor being forced down a central well 50 and saturated solution being withdrawn through output wells 5I and 52 spaced from the input well. Throttle valves 53 are provided', so that the flow from the output wells can be equalized. In cases where it is impossible to establish a lateral circulation naturally, the output wells can be drilled directionaly (in a way known per se) so as to slant towards the bottom of the input well. It is convenient to provide four output Wells in a square, with the input well at the center. Fig. 2 shows the input Well and two of the output wells.
The liquor coming up from the cavity is often more or less contaminated with mud, silt, sand, etc., and it is usually best to provide a closed settling chamber as indicated at 34, wherein the sludge may sette out of the hot liquor prior to passage t-o the spray cooler. Sludge may be removed through a sump outlet 35. A similar settler 36a is provided just before the spray cooler, as shown.
Some water is evaporated and lost in the spray cooling, and I accordingly add make-up water or brine as required through an inlet 38 to the mother liquor prior to" going to the heat exchanger and hea-ter. Water can also be added at this point to make up for any dissipation in the underground bed. Make-up water can also be added to the liquor prior to the spray cooling if desired, a valved inlet 31 being provided as shown.
The heater can be any suitable type of high pressure heater, and in the southwestern United States can conveniently be heated by natural gas, which occurs in regions adjacent the potash deposits. The heater, as well as the other ap# paratus elements which handle the circulating liquors, should be made of materials adapted to resist corrosion by the hot brines. The heater should be of a type adapted for easy cleaning, since some ofthe salines may deposit out from the liquors being heated, forming scale. Heaters constructed in a way similar to cracking stills, with detachable return bends giving access to the interior of the tubes for scraping, are useful.
In Fig. 3 1 have shown a modification of the invention in which the boiler is arranged to heat the liquor by indirect heat exchange, and which obviates scaling difliculties. The boiler is shown at 39. In this modification four concentric pipes are provided; the well 'casing I5, a pipe 40 for liquor. and two steam pipes 4I and 42. Pipes 4I and 42 may extend part way down the well, or clear to the bottom, as shown, and pipe 42 is capped at 43. In operation, high pressure steam is forced down and up the inner pipes, as indicated by the arrows, and liquor is circulated down pipe 40 and up between pipe 40 and the casing. The liquor is heated in its downward course. The boiler and steam tubes form a closed system and use plain water. Heat transfer media which give higher temperatures than water at the same pressure can be employed.
While the process has been described using a spray cooler, other cooling means can be employed. Sometimes suicient cooling can be had merely by running the brine issuing from the well, into a wide, shallow pool exposed to the atmosphere.
. In the preliminary step of heating up the potash deposits in the vicinity of the Well bore,
it is sometimes convenient to use steam instead of hot water. Superheated steam is injected down `the central pipe I6 and condenses on the wallsof the well cavity. The cavity walls can be heated much faster by steam than by circulating hot water.
In using NaCl brine as the circulating liquid, the NaCl stays mostly in solution when the liquor is cooled to deposit potash salts; a little may be deposited out with the potash salts due to the fact that the liquor is concentrated somewhat by loss of water in the evaporating step. This may be avoided by adding sufflcient water to the iiquor before it enters the sprays, to make up for loss of water by evaporation. The same considerations apply to certain other salts taken up by the brine, e. g. calcium sulfate and magnesium sulfate; which salts are even less soluble in Superheated wa'er or brines than in cold water or brines. These salts redeposit to some extent in the subterranean cavity. 'Ihe advantage of using NaCl is that it attacks polyhalite and similar refractory minerals aggressively. However, in such\procedure the potash is recovered as chloride (KC1; sylvite). Where recovery as sulfate is desired it is better to use plain Water if this is otherwise economical. Calcium chloride is even more aggressive than NaCl and is useful where the potash minerals are markedly refractory. In some cases I use CO2 in attacking the potash minerals, CO2 gas and Water being pumped down the well under heavy pressure. At the high hydrostatic pressure existing in deep wells (e. g. about 66 atmospheres at the bottom of a 2000 foot bore), the CO2 solution is and if it is desired to recover other compounds than potash, the heating and cooling temperay tures, and the degree of concentration of the liquor, are adjusted accordingly. Other saline deposits besides potash can be mined.
In mining potash from the New Mexican beds,
bromides and iodides build up in the circulatingV liquor. From time to time, the liquor can be treated, for instance with chlorine and steam to displace the bromine and iodine; these subl'as stances being recovered in elemental form by fractional condensation.
As stated, I have found that in a saturated solution of NaCl and KCl in contact with excess salts (sylvinite), the concentration of NaCl is actually somewhat less at high temperatures than at ordinary temperatures. Thus, the solubilities of NaCl and-KCl under such conditions at temperatures of 70 F. and 200 F. are as follows (grams per 100 ccm. of solution) Naci Kol Tomi rfgfi;
MWF 21.7 26.3 48.0 1.33 At70F 26.4 12.0 38.4 1.28
after precipitation of the potash salts, and sending it back into the cavity to replenish said body of liquor.
2. A method of winning potassium compounds from underground potash beds, which comprises establishing and maintaining in contact with such beds, a body of superheated aqueous solution of a compound selected from the class consisting of sodium chloride and calcium chloride, the solution being unsaturated with respect to potash, thereby disolving potash and forming a hot-walled cavity, withdrawing liquor from said body containing potash in solution as chloride, cooling the withdrawn liquor to cause precipitation of potassium chloride therefrom, removing the precipitated potasium chloride, reheating to a superheated condition the mother liquor remaining after precipitation of the potash salts, and forcing it back into the cavity to replenish said body of liquor.
3. A method of winning potash compounds from underground polyhalite beds, which comprises establishing and maintaining a body of highly heated saline liquor in contact with such beds for an extended period of contact so as to dissolve potash and form a hot-walled cavity, withdrawing liquor fromv said body containing potash salts in solution, cooling the withdrawn -liquor to cause precipitation of potash salts therefrom, removing the precipitated salts, reheating the remaining mother liquor to a temperature of at least 200 C. under superatmospheric pressure and forcing it back into the cavity to replenish said body of liquor.
4. In the mining of subterranean potash minerals occurring in beds, the cyclic process which comprises establishing and maintaining a hot body of concentrated saline solution at a temperature of 200 C. or higher in such a bed, the
hot saline liquorv being withdrawn, cooled to deposit crystalline potash salts and reheated whsfeby it becomes unsaturated with respect to potash, and returned to maintain the temperature and replenish the body, the rate of circulation being sufficiently slow that the reheated liquor comes substantially into equilibrium with the bed minerals.
5. A method of winning potassium compounds i from underground potash beds, winch comprises establishing a body of super-heated saline 'liquor in` contact with such beds to form a hot-walled cavity and dissolve potash, withdrawing liquor from said body containing potash salts in solution, cooling the withdrawn liquor to cause precipitation of potash salts therefrom, removing said precipitated salts, and maintaining said body of liquor in super-heated condition in contact with the potash beds, by supplying heat thereto and replenishing it with dilute liquor.
6. AV method of winning potash salts from potassium which comprises sending into contact 4 with such a deposit a bo'dy of superheated NaCl solution, removing and cooling the solution to crystallize out potassium chloride, reheating the solution to a superheated condition and returning the solution of NaCl in its super-heated state to the deposit for further attack thereon.
8. A method of winning potash salts from subterranean deposits, which comprises circulating downwardly into and through the deposits, superheated saline liquor unsaturated with respect to potash, at such rate as to provide an extended period of contact with a deposit, so as to take some of the potash therefrom, returning the hot solution upwardly, cooling the solution to a point sumcient to cause crystallization therefrom of at least some of the dissolved potash salts, reheating the solution to a superheated condition and-again returning it to extended contact with the deposits.
9. The method of claim 8 wherein the subterranean potash deposits are largely sylvinite (KCl, NaCl) and the circulating aqueous liquor contains NaCl and KCl.
10. 'Ihe method of claim 8 wherein the -subterranean potash deposits are largely polyhalite (2 CaSO4.MgSO4.KzSO4.2 H2O) and the aqueous liquor is reheated to at least 200 C. before it is returned to the deposits.
ROY CROSS.
.Patent lNo. 2,161,800.
CERTIFICATE 0F CORRECTION.
' June 15,A 1959.
)ROY CROSS. It is hereby certified V'that errorj appears inthe printed specification of the above' numbered patent Irequiring correction as follows: Page 1,'first column, line 1L, for the word "motor" read mother; 4line )42, for "externally" read extensively; line )45,.for "roller". read richer; saine page ,y second colfumn, line 11-12, for "ordinarily" read ordinary; page 2, first column,l line 5l, for the word "wall" read'w'elI; page 1|.,ffirst column, line 25,0.laim l, for "f" read for; line 1,0, claim 2,'for "disolving" read. dissolving; same page, second column, line c1aim8, before "superheated" insert the article a; and thatv the said Letters Patent shouldbe read with this correction thereinthat the same may conform tothe record of' the case inthel Pat? ent office.. Y v
Signed and sealed this 8th day of August, A. D. 1959.
Leslie Frazer, (Seal) Acting Commissioner of Patents.
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US136178A US2161800A (en) | 1937-04-10 | 1937-04-10 | Mining potash |
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US136178A US2161800A (en) | 1937-04-10 | 1937-04-10 | Mining potash |
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Cited By (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2682396A (en) * | 1948-09-17 | 1954-06-29 | Potash Company | Method for mining soluble ores |
US2861428A (en) * | 1953-12-28 | 1958-11-25 | Phillips Petroleum Co | Underground storage cavern having laterally spaced well and method therefor |
US2880587A (en) * | 1953-12-31 | 1959-04-07 | Phillips Petroleum Co | Hydraulic fracturing to develop underground storage caverns |
US3024612A (en) * | 1957-12-03 | 1962-03-13 | Texaco Development Corp | Method for removing calcium sulfate from underground storage cavities in salt formations |
US3034773A (en) * | 1958-03-24 | 1962-05-15 | Phillips Petroleum Co | Mining and extraction of ores |
US3050290A (en) * | 1959-10-30 | 1962-08-21 | Fmc Corp | Method of recovering sodium values by solution mining of trona |
US3058729A (en) * | 1960-01-08 | 1962-10-16 | Pittsburgh Plate Glass Co | Solution mining method |
US3135501A (en) * | 1962-05-01 | 1964-06-02 | Pittsburgh Plate Glass Co | In situ potassium chloride recovery by selective solution |
US3148000A (en) * | 1962-02-28 | 1964-09-08 | Pittsburgh Plate Glass Co | Solution mining of potassium chloride |
US3205012A (en) * | 1963-05-01 | 1965-09-07 | William B Dancy | Solution mining system using heat exchange tubes |
DE1224231B (en) * | 1961-05-26 | 1966-09-08 | Pittsburgh Plate Glass Co | Process for the extraction of potassium chloride from natural deposits containing KCl and NaCl |
US3386768A (en) * | 1966-09-29 | 1968-06-04 | Int Salt Co | Mining and refining soluble minerals |
US3421794A (en) * | 1966-09-27 | 1969-01-14 | Int Salt Co | Solution mining and refining minerals |
US3433530A (en) * | 1968-03-06 | 1969-03-18 | Ppg Industries Inc | Method of solution mining potassium chloride |
US3498674A (en) * | 1967-08-04 | 1970-03-03 | Dale M Matthews | Mining method and apparatus |
US3623769A (en) * | 1970-06-29 | 1971-11-30 | Armour & Co | Method and apparatus for solution mining |
US3823981A (en) * | 1973-04-04 | 1974-07-16 | Atomic Energy Commission | Situ leaching solvent extraction-process |
US3966541A (en) * | 1975-02-20 | 1976-06-29 | Abraham Sadan | Concentration of underground brines in situ by solar evaporation |
US3994531A (en) * | 1971-09-03 | 1976-11-30 | Continental Oil Company | Method of solution mining potassium chloride from subterranean deposits |
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 |
US4137720A (en) * | 1977-03-17 | 1979-02-06 | Rex Robert W | Use of calcium halide-water as a heat extraction medium for energy recovery from hot rock systems |
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 |
US4637462A (en) * | 1985-06-04 | 1987-01-20 | Grable Donovan B | Liquid mud ring control of underground liquids |
US4651824A (en) * | 1985-06-04 | 1987-03-24 | Gradle Donovan B | Controlled placement of underground fluids |
US6022080A (en) * | 1996-08-03 | 2000-02-08 | Kavernen Bau- Und Betriebs-Gmbh | Process and system for the solution mining of evaporites and preparation of saline solutions |
US20090309408A1 (en) * | 2008-06-17 | 2009-12-17 | Pinnacle Potash International, Ltd. | Method and system for solution mining |
US8991937B2 (en) | 2013-06-02 | 2015-03-31 | 101061615 Saskatcnewan Ltd. | Solution mining method with horizontal fluid injection |
WO2015023252A3 (en) * | 2013-08-12 | 2015-07-23 | Utah State University | Potash processing with mechanical vapor recompression |
CN110593917A (en) * | 2018-06-12 | 2019-12-20 | 江苏省制盐工业研究所有限公司 | Method for quickly building horizontal type oversized salt cavern storage |
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1937
- 1937-04-10 US US136178A patent/US2161800A/en not_active Expired - Lifetime
Cited By (41)
Publication number | Priority date | Publication date | Assignee | Title |
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US2682396A (en) * | 1948-09-17 | 1954-06-29 | Potash Company | Method for mining soluble ores |
US2861428A (en) * | 1953-12-28 | 1958-11-25 | Phillips Petroleum Co | Underground storage cavern having laterally spaced well and method therefor |
US2880587A (en) * | 1953-12-31 | 1959-04-07 | Phillips Petroleum Co | Hydraulic fracturing to develop underground storage caverns |
US3024612A (en) * | 1957-12-03 | 1962-03-13 | Texaco Development Corp | Method for removing calcium sulfate from underground storage cavities in salt formations |
US3034773A (en) * | 1958-03-24 | 1962-05-15 | Phillips Petroleum Co | Mining and extraction of ores |
US3050290A (en) * | 1959-10-30 | 1962-08-21 | Fmc Corp | Method of recovering sodium values by solution mining of trona |
US3058729A (en) * | 1960-01-08 | 1962-10-16 | Pittsburgh Plate Glass Co | Solution mining method |
DE1179890B (en) * | 1960-01-08 | 1964-10-22 | Pittsburgh Plate Glass Co | Method of breaking down potassium chloride from underground storage facilities |
DE1224231B (en) * | 1961-05-26 | 1966-09-08 | Pittsburgh Plate Glass Co | Process for the extraction of potassium chloride from natural deposits containing KCl and NaCl |
US3148000A (en) * | 1962-02-28 | 1964-09-08 | Pittsburgh Plate Glass Co | Solution mining of potassium chloride |
US3135501A (en) * | 1962-05-01 | 1964-06-02 | Pittsburgh Plate Glass Co | In situ potassium chloride recovery by selective solution |
US3205012A (en) * | 1963-05-01 | 1965-09-07 | William B Dancy | Solution mining system using heat exchange tubes |
US3421794A (en) * | 1966-09-27 | 1969-01-14 | Int Salt Co | Solution mining and refining minerals |
US3386768A (en) * | 1966-09-29 | 1968-06-04 | Int Salt Co | Mining and refining soluble minerals |
US3498674A (en) * | 1967-08-04 | 1970-03-03 | Dale M Matthews | Mining method and apparatus |
US3433530A (en) * | 1968-03-06 | 1969-03-18 | Ppg Industries Inc | Method of solution mining potassium chloride |
US3623769A (en) * | 1970-06-29 | 1971-11-30 | Armour & Co | Method and apparatus for solution mining |
US3994531A (en) * | 1971-09-03 | 1976-11-30 | Continental Oil Company | Method of solution mining potassium chloride from subterranean deposits |
US3823981A (en) * | 1973-04-04 | 1974-07-16 | Atomic Energy Commission | Situ leaching solvent extraction-process |
US3966541A (en) * | 1975-02-20 | 1976-06-29 | Abraham Sadan | Concentration of underground brines in situ by solar evaporation |
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 |
US4137720A (en) * | 1977-03-17 | 1979-02-06 | Rex Robert W | Use of calcium halide-water as a heat extraction medium for energy recovery from hot rock systems |
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 |
US4637462A (en) * | 1985-06-04 | 1987-01-20 | Grable Donovan B | Liquid mud ring control of underground liquids |
US4651824A (en) * | 1985-06-04 | 1987-03-24 | Gradle Donovan B | Controlled placement of underground fluids |
US6022080A (en) * | 1996-08-03 | 2000-02-08 | Kavernen Bau- Und Betriebs-Gmbh | Process and system for the solution mining of evaporites and preparation of saline solutions |
AU2009260878B2 (en) * | 2008-06-17 | 2012-05-24 | Pinnacle Potash International, Ltd. | Method and system for solution mining |
US7857396B2 (en) * | 2008-06-17 | 2010-12-28 | Pinnacle Potash International, Ltd. | Method and system for solution mining |
US20110080035A1 (en) * | 2008-06-17 | 2011-04-07 | Pinnacle Potash International, Ltd. | Method and System for Solution Mining |
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US20090309408A1 (en) * | 2008-06-17 | 2009-12-17 | Pinnacle Potash International, Ltd. | Method and system for solution mining |
EP2313609A4 (en) * | 2008-06-17 | 2013-08-28 | Pinnacle Potash International Ltd | Method and system for solution mining |
US8936320B2 (en) | 2008-06-17 | 2015-01-20 | Pinnacle Potash International, Ltd. | Method and system for solution mining |
US8991937B2 (en) | 2013-06-02 | 2015-03-31 | 101061615 Saskatcnewan Ltd. | Solution mining method with horizontal fluid injection |
US8998345B2 (en) | 2013-06-02 | 2015-04-07 | 101061615 Saskatchewan Ltd. | Solution mining method with elongate sump |
WO2015023252A3 (en) * | 2013-08-12 | 2015-07-23 | Utah State University | Potash processing with mechanical vapor recompression |
CN110593917A (en) * | 2018-06-12 | 2019-12-20 | 江苏省制盐工业研究所有限公司 | Method for quickly building horizontal type oversized salt cavern storage |
CN110593917B (en) * | 2018-06-12 | 2022-02-08 | 江苏省制盐工业研究所有限公司 | Method for quickly building horizontal type oversized salt cavern storage |
US20200080405A1 (en) * | 2018-09-06 | 2020-03-12 | Buffalo Potash Corp. | Downhole heating methods for solution mining |
US11634978B2 (en) | 2020-02-18 | 2023-04-25 | Canatech Management Services Inc. | Methods for recovering a mineral from a mineral-bearing deposit |
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