WO2009154676A1 - Method and system for solution mining - Google Patents
Method and system for solution mining Download PDFInfo
- Publication number
- WO2009154676A1 WO2009154676A1 PCT/US2009/002963 US2009002963W WO2009154676A1 WO 2009154676 A1 WO2009154676 A1 WO 2009154676A1 US 2009002963 W US2009002963 W US 2009002963W WO 2009154676 A1 WO2009154676 A1 WO 2009154676A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- brine
- mineral
- production
- heat exchanger
- injection
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 69
- 238000005065 mining Methods 0.000 title claims description 51
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims abstract description 410
- 239000012267 brine Substances 0.000 claims abstract description 409
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 254
- 239000011707 mineral Substances 0.000 claims abstract description 254
- 238000004519 manufacturing process Methods 0.000 claims abstract description 223
- 239000012530 fluid Substances 0.000 claims abstract description 89
- 239000013078 crystal Substances 0.000 claims abstract description 74
- 239000000243 solution Substances 0.000 claims abstract description 64
- 238000000926 separation method Methods 0.000 claims abstract description 54
- 239000002002 slurry Substances 0.000 claims abstract description 45
- 238000002347 injection Methods 0.000 claims description 123
- 239000007924 injection Substances 0.000 claims description 123
- 230000008569 process Effects 0.000 claims description 51
- 238000001816 cooling Methods 0.000 claims description 48
- 239000007787 solid Substances 0.000 claims description 32
- 239000002245 particle Substances 0.000 claims description 30
- 238000010899 nucleation Methods 0.000 claims description 14
- 239000000047 product Substances 0.000 claims description 14
- 238000012546 transfer Methods 0.000 claims description 14
- 239000007788 liquid Substances 0.000 claims description 13
- 238000010438 heat treatment Methods 0.000 claims description 11
- 238000000605 extraction Methods 0.000 claims description 10
- 238000001556 precipitation Methods 0.000 claims description 10
- 238000002425 crystallisation Methods 0.000 claims description 9
- 230000008025 crystallization Effects 0.000 claims description 9
- 230000009467 reduction Effects 0.000 claims description 7
- 239000002244 precipitate Substances 0.000 claims description 6
- 230000001376 precipitating effect Effects 0.000 claims description 6
- -1 whereby a cool Substances 0.000 claims description 3
- 238000011065 in-situ storage Methods 0.000 claims description 2
- 238000004513 sizing Methods 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 238000004891 communication Methods 0.000 claims 1
- 238000012216 screening Methods 0.000 claims 1
- 238000010924 continuous production Methods 0.000 abstract 1
- 235000010755 mineral Nutrition 0.000 description 175
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 97
- 239000001103 potassium chloride Substances 0.000 description 51
- 235000011164 potassium chloride Nutrition 0.000 description 51
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 49
- 235000002639 sodium chloride Nutrition 0.000 description 35
- PALNZFJYSCMLBK-UHFFFAOYSA-K magnesium;potassium;trichloride;hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-].[Cl-].[K+] PALNZFJYSCMLBK-UHFFFAOYSA-K 0.000 description 16
- 150000003839 salts Chemical group 0.000 description 14
- 239000010442 halite Substances 0.000 description 13
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 11
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 11
- 230000008901 benefit Effects 0.000 description 11
- 229940072033 potash Drugs 0.000 description 11
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 11
- 235000015320 potassium carbonate Nutrition 0.000 description 11
- 238000004090 dissolution Methods 0.000 description 9
- 238000001704 evaporation Methods 0.000 description 9
- 238000002386 leaching Methods 0.000 description 9
- 230000008020 evaporation Effects 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000013505 freshwater Substances 0.000 description 7
- 229910001629 magnesium chloride Inorganic materials 0.000 description 6
- 238000005057 refrigeration Methods 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 238000000354 decomposition reaction Methods 0.000 description 5
- 238000009938 salting Methods 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 239000004568 cement Substances 0.000 description 4
- 230000001419 dependent effect Effects 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000005086 pumping Methods 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000003570 air Substances 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 238000010587 phase diagram Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000003345 natural gas Substances 0.000 description 2
- 230000006911 nucleation Effects 0.000 description 2
- 238000005185 salting out Methods 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000011067 equilibration Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- WALYXZANOBBHCI-UHFFFAOYSA-K magnesium sodium trichloride hydrate Chemical compound O.[Cl-].[Na+].[Mg+2].[Cl-].[Cl-] WALYXZANOBBHCI-UHFFFAOYSA-K 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/28—Dissolving minerals other than hydrocarbons, e.g. by an alkaline or acid leaching agent
- E21B43/281—Dissolving minerals other than hydrocarbons, e.g. by an alkaline or acid leaching agent using heat
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L9/00—Rigid pipes
- F16L9/18—Double-walled pipes; Multi-channel pipes or pipe assemblies
- F16L9/19—Multi-channel pipes or pipe assemblies
Definitions
- the present invention pertains to mining and more particularly to solution mining of soluble minerals.
- Priority is claimed to U.S. Provisional Patent Application Serial No. 61/132,294 filed on 17 June 17 2008, and to U.S. Patent Application Serial No. 12/316,398 filed on 13 December 2008, each of which is inco ⁇ orated by reference in its entirety for all purposes.
- a cavern is formed by injecting a solvent, which is typically water, and saturating the resulting solution with a desired mineral to the extent possible before bringing it to the surface as a produced brine.
- a solvent typically water
- the solubility of the desired mineral in the produced brine is a function of temperature, and the underground deposit of the desired mineral is often at a temperature greater than the surface ambient temperature so that a relatively high concentration of the desired mineral is in the produced brine.
- the produced brine is often transported by pipeline to a processing plant, where it is cooled in refrigerated heat exchangers to below ambient temperature in order to cause a portion of the dissolved desired mineral to precipitate due to the reduction in temperature.
- the temperature of the produced brine may be reduced by evaporation of the solvent, which is typically water, to cause precipitation of solid crystals of the desired mineral.
- a slurry of the crystals of the desired mineral is processed to recover the crystals, and a depleted brine remains after the crystals are removed.
- the depleted brine can be returned to the source cavern.
- non-selective mining the depleted brine is disposed of as a waste product. Cooling by refrigeration and evaporation is energy intensive and expensive.
- U.S. Patent No. 3,348,883 issued to Jacoby et al. and incorporated by reference, teaches the use of two separate wells drilled into a relatively high temperature mineral deposit, where one of the wells is used for injection and one for production.
- a warm production brine is produced to the surface, where it is cooled in an evaporative heat exchanger to recover the desired minerals.
- This is not an optimum process in that evaporation can cause undesired minerals, such as halite, to precipitate, and the thermal energy in the production brine is wasted.
- With evaporative cooling very little of the original production brine will remain, and what does remain will be highly contaminated and not suitable for injection into the mineral deposit. In the case of either partial or complete evaporation, a significant quantity of water must be replaced.
- Water or oil is heated in a heat exchanger at the surface and passed downwardly through an annular space in a production well adjacent to a tube through which the production brine flows upwardly, and upon reaching the bottom of the production well, the oil or water returns to the heat exchanger through another annular space.
- U.S. Patent No. 3,058,729 issued to Dahms et al. and incorporated by reference, describes a method for solution mining potash, potassium chloride, in which a water solution was injected into a potash deposit and left for months to dissolve the potassium chloride. Brine rich in potassium chloride was produced and conveyed to a shallow cooling pond, where the ambient temperature was relatively cold. Potassium chloride crystals deposited in the pond, and a mother liquor was withdrawn from the pond. A small portion of the mother liquor was purged, and water was added to a large portion of the mother liquor to form the water solution that was fed to the potash deposit. This method requires a cold climate or supplemental means for cooling the produced brine.
- the produced brine became a slurry containing potassium chloride crystals as it was cooled.
- the potassium chloride crystals were separated and recovered using physical-separation equipment, such as a cyclone, leaving a brine solution that contained a lower concentration of potassium chloride referred to as a depleted brine.
- a portion of the depleted brine was recirculated to the shell and tube heat exchangers in the heat exchange crystallizer to cool the produced brine, which warmed the depleted brine.
- Fresh water was added to the warmed, depleted brine to form a solution that was injected into the potash deposit for dissolving the potassium chloride and forming the produced brine.
- the method described in the '916 patent requires equipment that is relatively expensive, complex and difficult to maintain and requires a high amount of energy to operate.
- the present invention provides in one embodiment a process for solution mining, in which an injection conduit is provided into a mineral deposit having a desired mineral.
- the injection conduit is adapted to convey an injection fluid into the mineral deposit for dissolving the desired mineral and forming a production brine.
- a production conduit is provided into the mineral deposit and is adapted to convey the production brine to the surface of the earth.
- Injection fluid is injected into the injection conduit, which forces the production brine to flow through the production conduit.
- the production brine is cooled as it is conveyed through a conveyance conduit and one or more heat exchangers to a separation plant. Cooling the production brine causes the desired mineral to precipitate thereby forming a slurry containing desired solid mineral crystals in a brine solution.
- the desired solid mineral crystals are separated from the brine solution in the separation plant, thereby forming a stream of liquid depleted brine and recovering solid mineral crystal product.
- the depleted brine is conveyed through the one or more heat exchangers to the injection conduit and injected as all or part of the injection fluid. Heat is exchanged between the production brine and the depleted brine in the one or more heat exchangers for cooling the production brine and for heating the depleted brine.
- the crystallization of the solid mineral crystal product is due to a reduction in temperature of the production brine that occurs between the mineral deposit and the separation plant due to a loss of heat from the production brine.
- the loss of heat from the production brine is due essentially to a transfer of heat from the production brine to the depleted brine in the heat exchanger and to loss of heat from the production brine to the ambient environment while being conveyed from the mineral deposit in the production conduit, the one or more heat exchangers, and the conveyance conduit to the separation plant.
- no powered heat exchangers are used in the process, and preferably, the only process energy consumed is the energy required for pumping the fluid through the mining system.
- the depleted brine is preferably warmed back to nearly the temperature of the mineral deposit, preferably without the use of external heating, which increases the leaching rate and the saturation level.
- the present invention provides in another embodiment a process for solution mining a mineral from an underground mineral source.
- the process includes providing an injection conduit into the mineral source adapted to convey an injection fluid into the mineral source for dissolving the mineral and forming a concentrated production brine and providing a production conduit into the mineral source adapted to convey the concentrated production brine to the surface of the earth.
- the injection fluid is injected into the injection conduit, and the concentrated production brine is conveyed to mineral-extraction equipment, where the mineral is extracted from the concentrated production brine to form a dilute brine stream.
- a heat exchanger is provided to exchange heat between the relatively warm concentrated production brine and the relatively cool dilute brine stream for cooling down the concentrated production brine so that a portion of the mineral will crystallize due to the lower temperature.
- the mineral-extraction equipment removes the crystallized mineral to form a mineral stream or slurry.
- the dilute brine stream is conveyed to the injection conduit, where it is used as the injection fluid, which may also contain some make-up water if needed. Alternatively, make-up water can be added by a separate pipe to the heat exchanger.
- brine remains essentially saturated after dissolving the mineral, but the amount of dissolved mineral in the fluid stream varies with temperature.
- a saturated brine having a certain temperature upon exit from a production well is referred to as concentrated brine. Upon cooling, crystals will form in the concentrated brine, forming a slurry of liquid with solid particles in the liquid.
- the solid particles can be removed from the slurry by various types of separation equipment. After the solid particles are removed from the slurry, a saturated brine remains that has a lower temperature than the concentrated brine, which is referred to as a dilute or depleted brine stream.
- a pipe-in-pipe heat exchanger is used for exchanging heat between the concentrated production brine and the dilute brine stream, and preferably, the pipe-in-pipe heat exchanger also serves as a significant means for conveying the concentrated production brine to the mineral-extraction equipment and for conveying the dilute brine stream to the injection conduit.
- the concentrated production brine is seeded to promote crystallization of the mineral, preferably with mineral particles recovered from the concentrated production brine.
- the present invention provides in another embodiment a system adapted for extraction of a mineral from an underground source of the mineral, where an injection tube extends from the surface of the earth into the underground source of the mineral and a production tube extends into the underground source of the mineral for conveying a warm, concentrated production brine containing the mineral from the underground source to the surface of the earth.
- Equipment for obtaining the mineral from the concentrated production brine provides a relatively cool, dilute brine obtained after the mineral is removed from the concentrated production brine.
- a heat exchanger is provided to exchange heat between the relatively cool, dilute brine and the relatively warm, concentrated production brine, and the cool, dilute brine is warmed to provide an injection fluid, which is pumped into the injection tube.
- the heat exchanger is preferably a pipe-in-pipe heat exchanger, but other types of exchangers such as a shell and tube can be used.
- the equipment for obtaining the mineral from the concentrated production brine preferably includes a separator, which is preferably a varisieve separator, preferably followed by a centrifuge. In the case of carnallite processing, the separator is preferably followed by a cracker (a decomposition tank) and then preferably by a centrifuge.
- the underflow from the centrifuge includes small particles, slimes, which can be used as seeds to promote crystallization in the production brine as it cools in the heat exchanger.
- a vortex separator is used to recover seed particles from the dilute, return brine, which contains the slime.
- the dilute brine carries the seed particles back to the heat exchanger, and the vortex separator removes some seed particles, which are then injected into the production brine near the warm end of the heat exchanger.
- a vortex separator has been described, but any device capable of separating the slimes or small seed particles from the liquid, dilute, return brine can be used.
- separation and sizing equipment is provided so that a portion of recovered mineral is separated by particle size, and a desired number of particles of a desired size are injected into the dilute, return brine for recovery in the vortex separator and injection into the warm production brine to promote formation of crystals of a desired size.
- One embodiment of the invention provides a process for mining a mineral from a site having an underground mineral source, where the site has been adapted with an injection conduit into the mineral source for conveying an injection fluid into the mineral source for dissolving the mineral and forming a concentrated production brine, and where the site has been further adapted with a production conduit into the mineral source for conveying the concentrated production brine to the surface of the earth.
- the process includes injecting the injection fluid into the injection conduit, conveying the concentrated production brine to mineral-extraction equipment, extracting the mineral from the concentrated production brine thereby forming a dilute brine stream and a mineral stream, disposing of the dilute brine stream, introducing a mineral- dissolving fluid to a heat exchanger; and exchanging heat between the concentrated production brine and the mineral-dissolving fluid in the heat exchanger.
- the mineral-dissolving fluid cools the concentrated production brine thereby forming crystallized mineral particles in the concentrated production brine, while the mineral-dissolving fluid is heated by the concentrated production brine.
- the injection fluid comprise.s the mineral-dissolving fluid after it is heated in the heat exchanger, and the mineral-dissolving fluid is typically fresh or saline water.
- a method for preparing a site for solution mining an underground source of mineral which includes installing injection tubing and production tubing extending between the surface of the earth and the underground source, installing equipment adapted for obtaining the mineral from a production brine, installing a heat exchanger between the production tubing and the equipment adapted for obtaining the mineral; and installing piping and a pump adapted to circulate fluid from the production tubing, through the heat exchanger, through the equipment adapted for obtaining the mineral and down the injection tubing, wherein the heat exchanger is adapted to exchange heat between fluid from the production tubing and fluid from the equipment adapted for obtaining the mineral, and wherein the heat exchanger is adapted to serve as the primary and most significant means for cooling the fluid from the production tubing and thereby precipitating crystals of the mineral.
- Fig. Ia is a schematic representation of a solution mining process according to the present invention in which an injection conduit is installed in one well that extends into a mineral deposit, and a production conduit is installed in another well that extends into the mineral deposit;
- Fig. Ib is a schematic representation of a solution mining process according to the present invention that uses a dual completion in which an injection conduit and a production conduit are each installed in a single well that extends into a mineral deposit;
- FIG. 2 is a simplified schematic representation of a solution mining process, according to the present invention, illustrating, in particular, a heat exchanger for crystallizing a desired mineral;
- FIG. 3 is a simplified schematic representation of a solution mining process, illustrating, in particular, equipment that may be used in a separation plant for recovering mineral product and for conveying depleted brine to the heat exchanger, according to the present invention.
- Valuable evaporite minerals are usually obtained by means of conventional mining, by solution mining, or by recovering the minerals from highly saturated lakes, such as the Dead Sea. In most of these cases it is necessary to form and process a solution of the minerals such that the desired mineral(s) precipitates from the solution.
- the present invention pertains to solution mining, where water is pumped into an evaporite ore body, typically a subterranean deposit. A desired mineral in the deposit is dissolved, and a solution containing the desired mineral is conveyed to the surface. At this point the desired mineral is recovered from the solution.
- One way to do this is by evaporation, either by using evaporation ponds in hot dry climates, or by mechanical heating and evaporation in other climates.
- Refrigeration is effective for minerals that have a strongly temperature dependent solubility, such as ores of potash (sylvite or carnallite, for example).
- the present invention concerns these latter types of minerals, where solubility is dependent on temperature.
- What minerals and how much of each will precipitate will depend on the temperature drop experienced at the surface and on the phase diagram for the system of dissolved minerals. It is desirable to maintain the temperature of a produced brine as high as possible as it rises to the surface so that the production string will not salt up and become blocked due to cooling-induced precipitation on the pipe wall.
- the temperature drop in a production string can be minimized by insulating the production string, and minerals that precipitate on the pipe wall can be removed by flushing the production string with fresh water periodically.
- Fig. Ia shows a system 10 for solution mining a mineral deposit D, according to the present invention.
- An injection well 12 is placed into mineral deposit D by drilling a well bore Bl from the surface into the deposit, placing injection conduit 12 in the well, and pumping cement Cl around the injection conduit to seal the annular space between the injection conduit 12 and the wall of the earthen well bore Bl .
- An injection well head 12a provides access to injection well 12 and provides a connection point with appropriate valves and pipe connections.
- a production well 14 having a production well head 14a is similarly installed in a well bore B2 and sealed with cement C2 to provide a conduit for producing fluid from deposit D.
- Mineral deposit D may be fractured to provide a flow path through deposit D from injection well 12 to production well 14, such as by pumping a fluid down injection well 12 at very high pressure.
- a solvent which is typically a water solution, is fed through a pipe 16 to a heat exchanger 18, which heats the solvent.
- the heated solvent flows through a pipe 20 to injection well head 12a and down injection well 12 into mineral deposit D.
- the solvent flows through mineral deposit D, dissolving one or more minerals in the deposit and forming a production brine having a concentration of a desired dissolved mineral(s).
- the temperature of deposit D and of the production brine is higher than the surface ambient temperature.
- the solubility of the desired mineral(s) is temperature dependent, where saturation in the production brine is at a higher concentration at a high temperature as compared to a low temperature. Thus, a greater quantity of the desired mineral can be dissolved in a given volume of the solvent at a higher temperature than at a lower temperature.
- the production brine flows upwardly through production well 14 to production well head 14a and through a pipe 22 to heat exchanger 18.
- the production brine is cooled as it flows through heat exchanger 18, causing solid crystals of the desired mineral(s) to form due to lower solubility at the lower temperature.
- a slurry of the solid crystals of the desired mineral(s) in the produced brine flows through a pipe 24, and the crystals are separated and recovered as explained below.
- a single well bore B3 is drilled through the earth into the mineral deposit D.
- An injection conduit I and a production conduit P are sealed in the well bore B3 with a cement C3.
- a well head H provides valves and connection points for the injection conduit I and the production conduit P. Since injection conduit I and production conduit P are in close proximity, it may not be necessary to fracture deposit D.
- a water solution is fed through a line 28 to a heat exchanger E, where the solution is warmed, and then through a line 30 to injection conduit I.
- a desired mineral in deposit D is dissolved by the water solution to produce a warm brine solution rich in the desired mineral, which is produced through production conduit P.
- Fig. 2 provides a simplified drawing of a solution mining process 40, according to the present invention.
- a single well bore B4 is drilled through the earth into a mineral deposit M.
- a casing or outer pipe 42 is sealed in well bore B4 with a cement C4.
- An inner pipe 44 is placed inside outer pipe 42, forming a concentric well string.
- An annular space 42a is defined by the outside surface of inner pipe 44 and the inside surface of outer pipe 42.
- Annular space 42a serves as an injection conduit, while inner pipe 44 serves as a production conduit.
- a water solution or solvent is fed through annular space 42a to mineral deposit M.
- a desired mineral(s) is dissolved, and a brine is formed that has a relatively high concentration of the desired mineral(s).
- the brine which is relatively warm due to the relatively warm temperature of the mineral deposit M, is produced through inner pipe 44 and conveyed to a well head 46.
- the concentric well string serves as a pipe-in-pipe heat exchanger, which provides advantages ⁇ the production brine tends to retain its relatively warm temperature, which minimizes salting out in the production tubing, and the injection fluid can be delivered to the deposit at about the same temperature as in the deposit, which helps to prevent cooling in the deposit and allows dissolution to take place at as high of a temperature as is naturally possible. While normally production will be through inner pipe 44, either inner pipe 44 or annular space 42a can be used for producing the brine, and the flow direction can be reversed, particularly for removing salt from the production conduit. Any of the well configurations shown in Figs. Ia, I b and 2 can be used, and any number of wells can be used to mine a mineral deposit.
- the mineral-rich brine thus formed is produced through inner pipe 44 and flows through well head 46 through a pipe 54 to an inlet 50b of an inside pipe 50c within heat exchanger 50. Inside pipe 50c runs through the length of heat exchanger 50 to an outlet 5Od to which a pipe 56 is connected.
- the produced, mineral-rich brine is cooled as heat in the produced brine is transferred to the water flowing through the annular space 50a. Since the solubility of the desired mineral(s) depends on the temperature of the solution that it is in, the desired mineral(s) precipitates as solid crystals within inside pipe 50c as the temperature of the produced brine drops, forming a slurry of the crystals in the brine solution.
- the slurry flows through line 56 to a separation plant 58.
- Separation or mineral-extraction equipment inside separation plant 58 removes the solid crystals of the desired mineral(s) from the slurry and leaves a brine solution from which the crystals have been removed that is referred to as a dilute or depleted brine.
- the solid crystals of the desired mineral(s) are recovered as a product 60.
- the depleted brine is at a substantially lower temperature than the warm, rich produced brine in line 54 and has a substantially lower concentration of the desired mineral(s) dissolved in it.
- the depleted brine is at about ambient temperature.
- the dilute or depleted brine is recirculated to the well, flowing through a pipe 62 to a high-pressure pump 64.
- Pump 64 pumps the depleted brine through a pipe 66 to the annular space 50a inside heat exchanger 50 to recirculate the depleted brine for additional solution mining of mineral of mineral deposit M.
- Pump 64 boosts the pressure of the dilute (return) brine so that it is sufficient to carry this brine to and through heat exchanger 50, into the cavern in deposit M, and then back through the production tubing 44, the heat exchanger 50, and back to the separation plant 58.
- separation plant 58 mineral particles, which are preferably sorted by size, are injected into the depleted brine for use in seeding the produced brine in line 54, although this step is not shown in Fig. 2.
- Separation plant 58 should have suitable equipment for separating crystals of the desired mineral from the slurry, preferably separating the crystals according to size, and injecting a portion of the crystals into the depleted brine for use in seeding the produced brine.
- the crystals serve as nucleation points for formation of crystals as the temperature of the brine drops. Further discussion on seeding is provided below.
- the depleted brine in pipe 66 which contains seed, mineral crystals, flows through a vortex separator 68, which removes most of the seed.
- Mineral crystals in a purge stream flow through a pipe 70 for injection into the produced brine in line 54 upstream of heat exchanger inlet 50b.
- a vortex separator is illustrated, but any equipment suitable for removing the seed crystals can be used.
- a seed solution can be conveyed from the separation plant 58 to the warm inlet 50b of heat exchanger 50.
- the depleted return brine flows through a pipe 72 into an inlet 5Oe into the annular space 50a at a cold end of heat exchanger 50 near produced brine outlet 5Od.
- Inlet 5Oe provides an opening through an outer pipe 50f that defines the outer surface of heat exchanger 50.
- the annular space 50a is defined by an inside surface of the outer pipe 50f and an outside surface of the inside pipe 50c.
- the depleted brine flowing out of vortex separator 68 into line 72 is generally at or near ambient temperature, which is generally relatively cool as compared to the formation temperature inside mineral deposit M and the temperature of the produced brine in line 54.
- Heat exchanger 50 is preferably a very long pipe-in-pipe heat exchanger or a number of shorter pipe-in-pipe heat exchangers arranged in series. Alternatively, heat exchanger 50 can be a number of shell and tube heat exchangers arranged in parallel, or any suitable means for heat exchange according to the present invention can be used as well.
- relatively cool depleted brine flows into annular space 50a of heat exchanger 50 through inlet 5Oe.
- the depleted brine mixes with water from source W in annular space 50a, forming an injection fluid, and after start-up, the amount of water W can be reduced according to need.
- the injection fluid flows through annular space 50a countercurrent to the flow of the produced brine within inside pipe 50c.
- Thermal energy in the warm, rich production brine flows through the wall of the inside pipe 50c into the injection fluid in the annular space 50a, which both cools the produced brine and warms the injection fluid that comprises the depleted brine from line 72 and the make-up water from line 48.
- Some thermal energy will also likely be lost to the ambient environment through the wall of the outer pipe 50f.
- Solid crystals of the desired mineral(s) are separated and recovered as product 60, and a depleted brine is recirculated by pump 64 to heat exchanger 50.
- Mineral seed is added to the depleted brine while in separation plant 58, and the seed is conveyed to the vortex separator 68 in the depleted brine by pump 64 and lines 62 and 66.
- the mineral seed is recovered with the vortex separator and conveyed through line 70 and injected into the produced brine in line 54.
- the depleted brine after the seed is removed in the vortex separator 68, flows into the heat exchanger 50 through line 72.
- a desired amount of fresh make-up water from source W is added through line 48 to form the injection fluid, which is heated by the produced brine in the heat exchanger 50.
- the injection fluid is conveyed to well head 46 through line 52 and injected into the mineral deposit M through annular space 42a in the concentric well string.
- the injection fluid leaving the heat exchanger in line 52 is reasonably warm since it is heated by the produced brine from a near-ambient temperature.
- the injection fluid flows countercurrently in well string annular space 42a to the produced brine flowing upwardly in the inner well string pipe 44, providing an insulating layer that helps to prevent a substantial loss of heat from the produced brine while warming the injection fluid to nearly the temperature of the mineral deposit M.
- the injection fluid entering the cavern in the mineral deposit M is thus reasonably warm, which improves the dissolution rate for dissolving the desired mineral(s) in the deposit M and increases the amount of the desired mineral that can be dissolved in a given quantity of the injection fluid since the solubility of the desired mineral(s) depends on the temperature of the injection fluid.
- the rich, more-concentrated produced brine is formed, which is at essentially the temperature of the mineral deposit provided the period of time was long enough to allow temperature equilibration.
- the produced brine is conveyed to heat exchanger 50 through inner well string pipe 44 and line 54 to continue the continuous cycle.
- the source W of the make-up water is often a water well, pond, lake or a source of salt water, but the water can also be transported and stored in a tank.
- the water is preferably added into heat exchanger 50 as shown in Fig. 2 or into line 72, but the make-up water can be injected into the dilute brine return line 62 at the separation plant 58.
- the depleted brine cannot carry seed crystals because the mineral crystals will dissolve in the diluted brine.
- a seed tank can be located near the warm end inlet 50b of the heat exchanger 50 with a pump for injecting the seeds into the production brine.
- One seed tank can feed multiple production wells.
- Fig. 3 a simplified process flow diagram 70 is shown for producing and processing a carnallite slurry, according to the present invention.
- the carnallite slurry is produced according to the process described with reference to Fig. 2, which is identified in Fig. 3 as step 72.
- step 72 includes placing a concentric well string into a subterranean mineral deposit having carnallite as the desired mineral.
- An injection fluid dissolves the carnallite, and a production fluid is formed that is relatively warm and rich in carnallite.
- the production fluid is produced in step 72 and passed through the inner pipe of a pipe-in-pipe heat exchanger in step 72.
- the production fluid is cooled in the heat exchanger in step 72, and a slurry containing carnallite crystals is formed in step 72.
- the slurry is conveyed through a pipe 74 to a separation plant 76, where the slurry is fed to a varisieve separator 78, which separates the solid crystals of carnallite from the liquid brine solution in the slurry, and about 90 to about 95 % of the liquid brine solution, referred to as a depleted brine, is recirculated through a pipe 80 to the heat exchanger in step 72, where heat is transferred from the produced brine to the depleted brine for cooling the produced brine and warming the depleted brine.
- the injection fluid comprises this warmed, depleted brine, which is used to dissolve more of the carnallite and form more production fluid in step 72 in a recirculation circuit.
- Fresh water is added through a pipe 86 to the carnallite crystals, causing the carnallite to decompose into solid potassium chloride, KCl, and liquid magnesium chloride, MgCl 2 , brine.
- a slurry containing the solid potassium chloride and liquid magnesium chloride is conveyed from decomposition tank 84 through a line 88 to a centrifuge 90. Centrifuge 90 separates the solid potassium chloride from the liquid magnesium chloride.
- the liquid magnesium chloride brine flows through a pipe 92 to a holding pond 94, which may cover as much as fifty (50) acres.
- Magnesium chloride product 96 is recovered from the holding pond 94 by conventional means.
- the solid potassium chloride recovered by centrifuge 90 is conveyed by a line 98 and then through a line 98a to a dryer 100 or through a line 98b to a wet storage tank 102, from which a wet potassium chloride product 104 can be loaded.
- Dryer 100 removes water from the wet potassium chloride, providing dry, solid KCl crystals, which are conveyed through a line 106 to a screen 108.
- Screen 108 separates the particles of potassium chloride into various size ranges, and the separated potassium chloride crystals are conveyed through one or more lines 1 10 to dry storage facilities 1 12. Dry potassium chloride product 1 14 is loaded onto trucks and/or rail cars. In the event that the produced crystals are not large enough to be commercial, a thickener and or a compactor can be added to the process.
- a portion of a specific size range of KCl particles is conveyed through a line 1 16 to the low-pressure intake of the return brine injection pump (not shown).
- Line 1 16 may comprise a conveyor belt and a hopper for injecting seed particles of the potassium chloride into line 80 at a controlled rate.
- the solid potassium chloride particles conveyed from screen 108 to depleted brine line 80 will serve as seeds in the production side of the heat exchanger in step 72, as was discussed above with reference to Fig. 2.
- the depleted, return brine in line 80 will have small particles of potassium chloride that passed through varisieve separator 78, so additional seeding through line 116 is optional, but preferred.
- the preferred particle size or the distribution of particle sizes and the number of particles for optimum seeding should be determined by experimentation. It is believed that fewer and larger seed crystals will result in formation of larger crystals, unless too few seeds are injected, and if too few seeds are added, a large portion of the flow of produced brine will not be seeded.
- the optimum size and amount of seeds will depend on the minerals involved and the heat exchanger conditions and design. Precipitation of the desired minerals can also be increased by injecting a brine into the heat exchanger that contains a dissolved mineral that will displace the desired mineral. An example of this would be the injection of a MgCl 2 saturated brine into a KCl brine in the heat exchanger.
- phase diagram for this mixture indicates that KCl can be preferentially precipitated.
- U.S. Patent No. 4,283,372 issued to Print et al. and incorporated by reference, describes a method for recovering alkali value from sodium bicarbonate-containing ore by utilizing an aqueous solvent containing ammonia.
- Figs. 2 and 3 together provide a simplified description of a method for solution mining an underground, in situ mineral source according to the present invention.
- a description is provided for producing brine containing a desired mineral, cooling the brine in a heat exchanger and thereby causing the desired mineral to precipitate, and transferring the heat from the produced brine to the depleted brine returned from the separation plant.
- the depleted brine is used to convey seed crystals from the separation plant to the heat exchanger, where vortex separator 68 removes the seed crystals for injection into the produced brine upstream of the heat exchanger.
- a description of one embodiment of a separation plant is provided, which describes separation and recovery of the desired mineral product and of seed crystals that can be used to seed the produced brine.
- the heat exchange system described for the present invention is also useful in situations where it is necessary or desirable to dispose of the dilute brine stream.
- a mineral-dissolving fluid which is typically fresh or saline water, is introduced into the heat exchanger, where the dilute or depleted brine stream would otherwise be introduced, which cools the produced brine while heating the mineral-dissolving fluid before it is injected into the mineral deposit.
- heat exchanger 50 in Fig. 2 many types of heat exchangers are applicable to this invention, provided that the precipitating crystals do not plug the heat exchanger and other requirements, such as heat transfer area, are satisfied.
- pipe-in-pipe heat exchanger 50 in Fig. 2 is particularly suitable for this application for the following reasons: it is inexpensive; it can be constructed and repaired in the field; it can be easily lined or coated to minimize salting; it can easily be elongated to reduce the average temperature drop across the wall to the warm fluid; and it can be used as a significant part of the fluid connection between the well and the separation plant. A high temperature drop across the exchanger wall promotes salting.
- Shell and tube heat exchangers which are typically used in plants because of their compactness, can also be used, but do not provide the above advantages. It is also possible to install a pipe-in-pipe heat exchanger in the production well itself, using smaller tubes to inject seeds and other brine if required. This would not normally be the preferred installation because of the difficulty of servicing the exchanger. However, with long experience with a given ore body, where service of the surface exchanger has become minimal, the in-the- well approach could become preferable in that it would make use of the concentric tubing already in place for injection into and production from the well.
- the concentric well string configuration illustrated in Fig. 2 effectively extends the heat exchanger into the well for added exchanger surface area, although it does not include the ability to seed or to inject a brine into production conduit 44 proximate to mineral deposit M for promoting crystallization in the production brine while in production conduit 44.
- auxiliary heat exchanger in addition to heat exchanger 50 in Fig. 2, although such an exchanger is not shown in the drawings. Many, if not most ore bodies, do not have a large enough temperature elevation to produce sufficient precipitation at the surface.
- an auxiliary external heat exchanger may be used.
- the auxiliary heat exchanger can be installed in line 52 in Fig. 2 between heat exchanger 50 and the injection well head 46 to heat the injection fluid.
- the source of heat for the auxiliary heat exchanger can be low grade natural gas, process heat such as from a power plant, solar heat, etc. At least part of the heat generated by the auxiliary heat exchanger would be recovered by heat exchanger 50 from the brine produced from the cavern.
- Warmer injection fluid would yield a production brine containing a higher concentration of the desired mineral due to a warmer temperature in the production brine. Whether this approach is economical depends on the cost of the auxiliary energy source and on the cost of alternative methods for recovering the desired mineral.
- using an auxiliary heat exchanger to heat the injection fluid has advantages over using a different type of cooling system for cooling the produced brine in that virtually any source of auxiliary heat can be used, in the simplicity of the equipment (particularly the pipe-in-pipe heat exchanger), and in the fact that the natural heat in the mineral deposit is recovered and used productively. If the heated injection brine is warmer than the ore body, it would be preferable to use injection and production conduits that are separated rather than a concentric pipe string.
- the present invention provides a system and a process for solution mining in which a heat exchanger is used to cool production brine containing a dissolved mineral coming from an ore body, such that the mineral precipitates, while previously depleted cool brine in a heat exchange relationship with the produced brine, is warmed and returned to the cavern for further mineral dissolution.
- the heat exchanger is of simple pipe-in-pipe design.
- the heat exchanger preferably forms a portion of the fluid connection between the well and a mineral-recovery process plant, which reduces piping costs.
- a pipe-in-pipe type of exchanger can be installed in the production well itself instead of on the surface (or in addition to a surface-mounted heat exchanger), with tubing attached thereto for the injection of seeds and other brine as desired.
- Warmed, re-injected brine is preferably in a heat exchange relationship with the tubing carrying the production brine in the well from the cavern, minimizing the cooling of the production brine and thus minimizing precipitation in the production tubing.
- a second heat exchanger can be placed between the first heat exchanger and the wellhead in order to further warm the depleted, re-injected brine beyond the capability of the first exchanger, where the second heat exchanger uses a source of heat other than that coming from the production well.
- the heat exchanger area can be increased if desired so as to reduce the mean temperature across the inner pipe wall of the heat exchanger, thus lowering the temperature difference between the wall and the production brine and thereby reducing potential for salting on the heat exchanger wall.
- the present invention preferably further provides seeds of the desired mineral selected for size and number that are injected into the brine production side of the heat exchanger to form nuclei to promote precipitation of the mineral, the amount and size distribution of such injection being used to determine the mineral crystal size emanating from the exchanger and to minimize salting on the exchanger wall.
- the precipitating side of the heat exchanger is coated or lined with a substance that minimizes precipitation on the exchanger wall.
- This invention improves upon both the refrigeration-induced precipitation process and the evaporative process. With respect to the former it provides an enormous simpler and lower cost capital investment and a very much lower operating cost in terms of energy used.
- selective mining minimizes the amount of water used, primarily make-up and water for decomposition of a mineral like carnallite, and there is almost zero waste left on the surface. This is in stark contrast to most solution mining projects.
- the present method can use fresh water or saline water. A mine using this process may well be one of the cleanest mines in existence. With non-selective mining, saline water can be used, and subsurface brine disposal would be preferred.
- the first-stage heat exchange crystallizing station preferably includes initially passing the produced brine through a multi-stage vacuum growth-type crystallizer.
- the present invention is an improvement over the prior art method described in the '916 patent in that the second-stage cooler and the final crystallizing station are eliminated with the present invention.
- the second-stage atmospheric cooler in the '916 patent is essentially a cooling tower in which the brine flows downwardly over a set of baffles while a fan draws air upwardly through the baffles for cooling the brine by sensible heat exchange and by evaporating water from the brine.
- the heat in the produced brine is lost to the atmosphere, and the cooling tower is relatively expensive to build and maintain as compared to the heat exchanger in the present invention.
- the heat exchanger in the present invention takes full advantage of the heat in the mineral deposit in that the heat in the produced brine is nearly fully recovered in the heat exchanger of the present invention.
- the first-stage heat exchange crystallizing station comprising shell and tube heat exchangers described in the '916 patent exchange heat between the produced brine and the depleted, return brine
- the recovery of the heat in the produced brine is quite limited as evidenced by the need to have the second-stage atmospheric cooler in even cold climates, and additionally, the third-stage refrigerative cooling in climates that are not cold.
- the heat exchanger in the present invention is adapted to take advantage of heat transfer from the produced brine to the ambient environment and to have sufficient heat transfer area between the produced brine and the depleted, return brine to sufficiently cool the produced brine so that a substantially greater amount of potassium chloride crystals is recovered than could be recovered using the first-stage heat exchange crystallizing station alone without the second-stage atmospheric (evaporative) cooler and without the third-stage refrigerative cooler.
- the heat exchanger in the process of the present invention gradually reduces the temperature of the production brine to a point where a desired or optimal amount of the produced mineral is crystallized in a single stage and in a single and simple piece of equipment, which is the heat exchanger.
- the '916 patent describes a plurality of shell and tube heat exchangers in which some limited amount of heat is transferred from the produced brine to the depleted, return brine
- the '916 patent does not contemplate sufficiently reducing the temperature of the produced brine to adequately crystallize the desired mineral using only the depleted, return brine and ambient conditions to effect the required cooling of the produced brine.
- the '916 patent instead contemplated second-stage evaporative cooling and third-stage refrigerative cooling.
- the present invention particularly contemplates a pipe-in-pipe heat exchanger, which should be designed to reduce the temperature of a produced brine an amount comparable to the reduction that would be achieved by the heat exchangers, evaporative coolers and refrigerative coolers described in the '916 patent.
- the present invention provides improvements comprising: (i) eliminating the second-stage cooler and the final crystallizing station; (ii) using a pipe-in-pipe heat exchanger instead of the first-stage heat exchange crystallizing station comprising shell and tube heat exchangers for exchanging heat between the produced brine and the relatively-cool depleted brine, wherein the pipe- in-pipe heat exchanger is adapted to take advantage of heat transfer from the produced brine to the ambient environment and to have sufficient heat transfer area between the produced brine and the depleted brine to sufficiently cool the produced brine so that a substantially greater amount of potassium chloride crystals is recovered than could be recovered using the first-stage heat exchange crystallizing station alone without the second-stage evaporative cooler and without the third-stage crystallizing station that uses refrigerative cooling.
- the reduction in the temperature of the concentrated production brine between the production conduit and the separation plant is achieved without using significant evaporative cooling and without using significant refrigeration.
- the reduction in the temperature of the concentrated production brine between the production conduit and the separation plant is achieved essentially by transferring heat energy from the concentrated production brine to the dilute brine stream in the one or more heat exchangers and by a transfer of heat energy from the concentrated production brine to the ambient environment through the pipe.
- the heat exchange system of the present invention which is used to cool the production brine, employs no significant man-made source of energy to cool the production brine.
- the heat exchange system of the present invention thus serves as a single crystallizer as compared to the solution mining process described in the '916 patent, which requires a first stage comprising shell and tube heat exchangers, a second stage evaporative cooling system that uses something like a cooling tower and a refrigeration system as a third stage, if needed depending on the ambient temperature conditions.
- the present invention uses the ambient environment as a heat sink (through natural convective loss of thermal energy) for cooling the produced brine, but most of the thermal energy lost from the produced brine (as it cools to precipitate the desired mineral) is recovered in the depleted brine and returned to the mineral deposit (so minimal thermal energy is lost from the mineral deposit). If the thermal energy losses to the ambient environment are too great, auxiliary heat should be added to the depleted brine before it is injected into the mineral deposit. Additionally, the exchanger, surface pipelines and the process equipment can be insulated to minimize these losses.
- the present invention further contemplates a long distance between the well head and the separation plant, and in the prior art a pipe would have been installed to convey the production brine and/or slurry to the separation plant, which would likely also include equipment such as described in the '916 patent for cooling the produced brine.
- a second pipe is installed in a concentric configuration around the pipe used to convey the production brine to the separation plant, which then provides the pipe-in-pipe heat exchanger of the present invention.
- the inside walls of the pipe carrying the production brine through the heat exchanger of the present invention can be easily coated or lined to inhibit salt formation on the inside walls of the pipe, and the minimal temperature difference between the produced brine on one side of the heat exchanger and the depleted brine on the other side further reduces the tendency for salt to accumulate on the inside walls of the production conduit in the heat exchanger of the present invention.
- the present invention offers a number of benefits and advantages as compared to prior art systems typified by the '916 patent.
- the depleted brine conveyed to the heat exchanger is at near-ambient temperature, which provides cooling for the production brine in the heat exchanger.
- the temperature of the production brine as it exits the heat exchanger is also at near-ambient temperature, although at a higher temperature than the depleted brine.
- the temperature difference between the production brine at its exit end of the heat exchanger and the depleted brine at its entrance end of the heat exchanger is minimal, which helps to minimize salting out on the inside wall of the heat exchanger on the production-brine side where precipitation of mineral occurs.
- Factors to consider in the overall energy balance include the thermal energy that the production brine will have as it leaves the mineral deposit, as the source of the thermal energy is the elevated temperature of the mineral deposit compared to the ambient surface temperature, losses in the production conduit primarily to the depleted brine injection fluid in a concentric tubing arrangement as described with reference to Fig.
- Heat transfer to the ambient environment depends on the ambient temperature, which is generally variable.
- a pipe-in-pipe heat exchanger can be buried below ground at the earth's surface, which would provide a reasonably constant ambient temperature and eliminate some of the variability in the exit temperature of the production brine from the heat exchanger, although the depleted brine would still be subject to variability because the separation equipment would be located presumably in an open-air environment.
- a number of factors should be considered in the design of the one or more heat exchanger(s).
- the preferred heat exchanger of the present invention is envisioned as a single pipe-in-pipe heat exchanger having a very long length, possibly about a mile in length.
- This type of exchanger can be constructed on-site where the mine is located.
- a single separation plant can accommodate a number of production wells, and the production brine from each production well can be conveyed from its well to the separation plant through a pipe-in-pipe heat exchanger.
- heat exchangers can be used, and more than one heat exchanger can be used in either a parallel or a serial combination or in a mix of parallel and serial.
- a standard-length, pipe-in-pipe heat exchanger may be available off-the-shelf, and multiple units can be assembled in series to convey the production fluid to the separation plant while exchanging heat with the depleted brine.
- Heat exchanger selection and design should be based on factors including capital cost, operating cost, maintenance - particularly with respect to salt plugging and corrosion, and ease of installation and operation.
- the heat exchanger should be designed to provide essentially all of the reduction in temperature of the production brine required to yield a desired production of the desired mineral, taking into account the net loss of thermal energy to the ambient environment.
- an evaporite bed consisting of halite (NaCl) and sylvite (KCl) has a temperature of 150 0 F as obtained from a down-hole temperature survey.
- the bed is 50% sylvite and 50% halite, which allows the bed to be selectively leached. In selective leaching only the more soluble sylvite is dissolved, and the halite remains in place.
- Mining is initiated by performing an undercut at the bottom of the bed. This is done by installing an immiscible fluid like oil a few feet above the bottom of the target bed. Solution mining then takes place under the pad, mining in a radial direction away from the well.
- the production brine drops nearly to a local ambient temperature of about 60 0 F, at which point the KCl concentration has dropped to about 10%, a drop of about 6% by weight, which forms a slurry of KCl crystals in the produced brine.
- the slurry flows to a process or separation plant, where solid KCl crystals above a certain size are separated and processed as described in connection with Fig. 3. With solids thus removed, a now- depleted brine is returned through a separate pipe to the heat exchanger using high- pressure pumps, where it is heated by warm production brine, and injected back into the cavern to continue the process.
- the depleted brine recovered at the separation plant is still saturated in KCl, but the brine is at the lower ambient temperature so less KCl is soluble in the brine at the lower temperature. Because the KCl precipitated in the heat exchanger, where no halite is available, the brine is no longer saturated in halite, and can be considered a dilute brine in this sense. Leaching continues in the cavern until the top of the ore bed is reached and another well must be drilled, assuming there is only one bed in the well.
- This example concerns solution mining of sylvite, as opposed to carnallite, and the decomposition tank used in the solution mining process for carnallite described with reference to Fig. 3 is not needed for mining sylvite.
- the exact dimensions of the heat exchanger, length and diameter, and its heat transfer area should be determined by numerical analysis using the specific conditions of a mining project.
- the high KCl content in the ore allows for selective leaching.
- non-selective leaching can also be used with the present invention. If the ore body is for instance 25% KCl, selective leaching would probably not be successful. In this case, fresh or saline water can be injected into the heat exchanger, where before the return, depleted brine was injected.
- the fresh or saline water is warmed in the heat exchanger by the produced brine before injection into the mine, and the higher temperature of the dissolution fluid increases the rate of dissolution and possibly the amount of KCl carried in the produced brine formed, depending on whether equilibrium is reached with the temperature of the body of ore.
- KCl is precipitated as before and is separated in the plant.
- the now dilute brine is disposed of, typically in a disposal well, but some could also be sold for different uses.
- This brine is replaced by fresh or saline water as discussed above. Again, since the return water is too dilute to maintain seeds, a separate seed injection method is required. This could be a seed tank as discussed above or a small separate seed pipeline.
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
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BRPI0915309A BRPI0915309B1 (en) | 2008-06-17 | 2009-05-13 | processes for solution mining and for preparing a site for solution mining of an underground mineral source as well as an adapted system for extracting a mineral from an underground mineral source |
MX2010013904A MX348221B (en) | 2008-06-17 | 2009-05-13 | Method and system for solution mining. |
ES09766990.7T ES2623473T3 (en) | 2008-06-17 | 2009-05-13 | Method and system for dissolution mining |
EP09766990.7A EP2313609B1 (en) | 2008-06-17 | 2009-05-13 | Method and system for solution mining |
RU2011100474/03A RU2472927C2 (en) | 2008-06-17 | 2009-05-13 | Solution mining method and system |
CN200980123069.0A CN102066692B (en) | 2008-06-17 | 2009-05-13 | Method and system for solution mining |
AU2009260878A AU2009260878B2 (en) | 2008-06-17 | 2009-05-13 | Method and system for solution mining |
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US12/316,398 US7857396B2 (en) | 2008-06-17 | 2008-12-13 | Method and system for solution mining |
US12/316,398 | 2008-12-13 |
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CN (1) | CN102066692B (en) |
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ES2623473T3 (en) | 2017-07-11 |
US7857396B2 (en) | 2010-12-28 |
US20110080035A1 (en) | 2011-04-07 |
US8936320B2 (en) | 2015-01-20 |
RU2011100474A (en) | 2012-07-27 |
MX348221B (en) | 2017-06-02 |
BRPI0915309A2 (en) | 2015-10-27 |
AU2009260878A1 (en) | 2009-12-23 |
CN102066692B (en) | 2014-10-15 |
CA2666951C (en) | 2010-06-08 |
EP2313609A4 (en) | 2013-08-28 |
MX2010013904A (en) | 2011-03-24 |
US20090309408A1 (en) | 2009-12-17 |
RU2472927C2 (en) | 2013-01-20 |
US20140326354A1 (en) | 2014-11-06 |
EP2313609B1 (en) | 2017-03-15 |
CN102066692A (en) | 2011-05-18 |
EP2313609A1 (en) | 2011-04-27 |
CA2666951A1 (en) | 2009-08-11 |
BRPI0915309B1 (en) | 2019-08-27 |
AU2009260878B2 (en) | 2012-05-24 |
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