US20130161200A1 - Magnesium recovery method and magnesium recovery apparatus - Google Patents
Magnesium recovery method and magnesium recovery apparatus Download PDFInfo
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- US20130161200A1 US20130161200A1 US13/820,630 US201113820630A US2013161200A1 US 20130161200 A1 US20130161200 A1 US 20130161200A1 US 201113820630 A US201113820630 A US 201113820630A US 2013161200 A1 US2013161200 A1 US 2013161200A1
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
- C02F1/46104—Devices therefor; Their operating or servicing
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01F—COMPOUNDS OF THE METALS BERYLLIUM, MAGNESIUM, ALUMINIUM, CALCIUM, STRONTIUM, BARIUM, RADIUM, THORIUM, OR OF THE RARE-EARTH METALS
- C01F5/00—Compounds of magnesium
- C01F5/14—Magnesium hydroxide
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/58—Treatment of water, waste water, or sewage by removing specified dissolved compounds
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
- C25B1/04—Hydrogen or oxygen by electrolysis of water
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/18—Alkaline earth metal compounds or magnesium compounds
- C25B1/20—Hydroxides
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B15/00—Operating or servicing cells
- C25B15/08—Supplying or removing reactants or electrolytes; Regeneration of electrolytes
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/461—Treatment of water, waste water, or sewage by electrochemical methods by electrolysis
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/46115—Electrolytic cell with membranes or diaphragms
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2201/00—Apparatus for treatment of water, waste water or sewage
- C02F2201/46—Apparatus for electrochemical processes
- C02F2201/461—Electrolysis apparatus
- C02F2201/46105—Details relating to the electrolytic devices
- C02F2201/4618—Supplying or removing reactants or electrolyte
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2209/00—Controlling or monitoring parameters in water treatment
- C02F2209/06—Controlling or monitoring parameters in water treatment pH
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F9/00—Multistage treatment of water, waste water or sewage
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- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
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- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
- Y02P20/133—Renewable energy sources, e.g. sunlight
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- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W10/00—Technologies for wastewater treatment
- Y02W10/30—Wastewater or sewage treatment systems using renewable energies
- Y02W10/37—Wastewater or sewage treatment systems using renewable energies using solar energy
Abstract
In the magnesium recovery method and magnesium recovery apparatus, anode electrolyzed water (7 a) and cathode electrolyzed water (7 b) produced by electrolysis of seawater are separated, alkaline material is inputted into the anode electrolyzed water to adjust pH, magnesium is precipitated as magnesium hydroxide in the cathode electrolyzed water, and recovered, and the anode electrolyzed water after pH adjustment and cathode electrolyzed water after carbonate fixation are intermixed, and discharged in a state where a pH of the intermixed water is identical to a pH of the seawater. As a result, magnesium can be recovered from seawater while minimizing impact on the environment.
Description
- The present invention relates to a method and apparatus for recovering magnesium from seawater by electrolysis of seawater.
- Priority is claimed on Japanese Patent Application No. 2010-203353, filed Sep. 10, 2010, the content of which is incorporated herein by reference.
- In recent years, high specific strength magnesium has garnered attention as a next-generation structural material, and its demand is expected to increase hereafter. However, magnesium, which is primarily refined from the mineral, is unevenly distributed in limited geographical areas, and it would be desirable to establish procurement methods apart from importation of magnesium in order to secure stable supply in the future.
- As is well known, magnesium exists as a mineral, and is also contained in seawater. Accordingly, if magnesium could be recovered from seawater, it would greatly contribute to stable supply of magnesium. On the other hand, when recovering large quantities of magnesium from seawater, there is the possibility of impacting the environment, such as by changing seawater composition. Accordingly, magnesium recovery from seawater must be conducted without impact on the environment.
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Patent Document 1 shows an electrolysis tank for obtaining fresh water, chlorine gas, and magnesium hydroxide from seawater, andPatent Document 2 shows a method in which pH of deep seawater is electrolyzed, or pH is raised by addition of alkali, and hydroxides such as Mg and Ca are precipitated, and recovered as precipitate. - Patent Document 1: Japanese Unexamined Patent Application, First Publication No. S51-77586
- Patent Document 2: Japanese Unexamined Patent Application, First Publication No. 2007-167786
- In light of the pertinent circumstances, the present invention offers a magnesium recovery method and magnesium recovery apparatus which are capable of recovering magnesium from seawater without imposing burdens on the environment.
- The present invention pertains to a magnesium recovery method including: electrolyzing seawater; separating anodic electrolyzed water and cathodic electrolyzed water produced by electrolysis of the seawater; inputting alkaline material into the anodic electrolyzed water to adjust pH; precipitating magnesium as magnesium hydroxide in the cathodic electrolyzed water, and recovering the magnesium hydroxide; and intermixing the anodic electrolyzed water after pH adjustment and the cathodic electrolyzed water after recovery of the magnesium hydroxide and discharging the intermixed water in a state where a pH of the intermixed water is identical to a pH of the seawater.
- In this case, the alkaline material may be waste concrete. Iron, which is a soluble metal, may be used in the anode-side electrode to cause dissolution of ferric ions in the anodic electrolyzed water in the seawater electrolysis process.
- In addition, the present invention pertains to a magnesium recovery apparatus, including: an electrolysis tank having an anode and a cathode; a barrier film which partitions an interior of the electrolysis tank into an anode-side region containing the anode, and a cathode-side region containing the cathode; a first treatment tank which stores anodic electrolyzed water produced in the anode-side region; a second treatment tank which stores cathodic electrolyzed water produced in the cathode-side region; a power-supply unit which supplies power to the anode and the cathode; an alkaline material input device which inputs alkaline material to the first treatment tank; and a recovery unit which recovers magnesium hydroxide precipitated in the second treatment tank, in which wastewater from the first treatment tank and wastewater from the second treatment tank are intermixed, and discharged in a state where a pH of the intermixed water is identical to a pH of seawater.
- In this case, the power-supply unit may have at least one photovoltaic cell, fuel cell, wind power generator, wave power generator, ocean thermal power generator, or solar thermal power generator. The power-supply unit may contain a fuel cell which uses hydrogen gas generated on the cathode-side region, and oxygen gas generated on the anode-side region. The alkaline material inputted from the alkaline material input device may be waste concrete. Furthermore, the anode may contain iron as a consumable electrode, and the consumable electrode may dissolve ferric ions.
- According to the magnesium recovery method of the present invention, seawater is electrolyzed, anodic electrolyzed water and cathodic electrolyzed water produced by the electrolysis of seawater are separated, alkaline material is inputted into the anodic electrolyzed water to adjust pH, magnesium is precipitated as magnesium hydroxide in the cathodic electrolyzed water, and recovered, and the anodic electrolyzed water after pH adjustment and the cathodic electrolyzed water after magnesium hydroxide recovery are intermixed, and discharged with a pH identical to that of seawater. Consequently, according to the present invention, magnesium can be recovered from seawater without impact on the environment.
- In the magnesium recovery method of the present invention, it is possible to concomitantly perform treatment of industrial waste products when using waste concrete as the alkaline material.
- In the magnesium recovery method of the present invention, when using iron, which is a soluble metal, in the anode-side electrode, ferric ions are dissolved in the anodic electrolyzed water in the seawater electrolysis process, and ferric ions that are a nutrient of phytoplankton are supplied into the ocean. As a result, propagation of phytoplankton is promoted, achieving fixation of carbon dioxide gas by phytoplankton.
- According to the magnesium recovery apparatus of the present invention, there is provided: an electrolysis tank which has an anode and a cathode; a barrier membrane which partitions the interior of the electrolysis tank into an anode-side region containing the anode, and a cathode-side region containing the cathode; a first treatment tank which stores anodic electrolyzed water produced in the anode-side region; a second treatment tank which stores cathodic electrolyzed water produced in the cathode-side region; a power-supply unit which supplies power to the anode and the cathode; an alkaline material input device which inputs alkaline material into the first treatment tank; and a recovery unit which recovers magnesium hydroxide precipitated in the second treatment tank, in which by intermixing wastewater from the first treatment tank and wastewater from the second treatment tank, wastewater is discharged with a pH identical to that of seawater. Consequently, it is possible to recover magnesium from seawater without impact on the environment.
- In the magnesium recovery apparatus of the present invention, when the power-supply unit has at least one photovoltaic cell, fuel cell, wind power generator, wave power generator, ocean thermal power generator, or solar thermal power generator, it is possible to recover magnesium without impact on the environment.
- In the magnesium recovery apparatus of the present invention, when the power-supply unit contains a fuel cell which uses hydrogen gas generated on the cathode side, and oxygen gas generated on the anode side, a portion of the power expended in seawater electrolysis is again used in seawater electrolysis. Consequently, energy conservation is achieved.
- In the magnesium recovery apparatus of the present invention, when the alkaline material inputted from the alkaline material input device is waste concrete, treatment of waste concrete which is an industrial waste product can be concomitantly performed.
- In the magnesium recovery apparatus of the present invention, when the anode includes iron as a consumable electrode, the consumable electrode dissolves ferric ions, thereby supplying ferric ions, which are a nutrient of phytoplankton, into the ocean. As a result, the excellent effects are obtained that propagation of phytoplankton is promoted, and fixation of carbon dioxide gas by phytoplankton is achieved.
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FIG. 1 is a schematic view of an embodiment of the present invention. -
FIG. 2 is a graph which shows cathode current density and the precipitation ratio of CaCO3 and Mg(OH)2 in the embodiment. -
FIG. 3 is a block diagram which shows material balance in the embodiment of the present invention. -
FIG. 4 is a schematic block diagram which shows the magnesium recovery apparatus of an embodiment of the present invention. - Embodiments of the present invention are described below with reference to drawings.
- First, the principles of an embodiment of the present invention are described in
FIG. 1 . - In
FIG. 1 , 1 indicates an electrolysis tank, 2 indicates a first treatment tank, and 3 indicates a second treatment tank. - The
electrolysis tank 1 has anelectrolytic treatment container 4 made of corrosion-resistant material such as stainless steel, and theelectrolytic treatment container 4 has aninlet 5 at the upstream end, and anoutlet 6 at the downstream end.Seawater 7, which flows in from theinlet 5, runs uniformly through the interior of theelectrolytic treatment container 4, and is discharged from theoutlet 6. - Various methods may be adopted as a method of forming the flow of the
seawater 7. For example, theelectrolytic treatment container 4 may be submerged in water to utilize ocean current, and have theseawater 7 flow through the interior of theelectrolytic treatment container 4; or a screw or the like may be provided in theinlet 5 to create water flow by rotating this screw by a motor; or theseawater 7 may be taken in by a pump or the like, and supplied to theinlet 5. - A
barrier membrane 8 is provided inside theelectrolytic treatment container 4 in the flow direction of the seawater. Thebarrier membrane 8 partitions the interior of theelectrolytic treatment container 4 in two, with the result that a flow of theseawater 7 separated by thebarrier membrane 8 is formed inside theelectrolytic treatment container 4. - The
barrier membrane 8 uses a material and structure through which electric current passes and which prevent or inhibit intermixture of the separated streams. For example, one may use unglazed plates in tile form laid out in rows, or porous sheets or the like made of synthetic resin. - In the case where the interior of the
electrolytic treatment container 4 is partitioned by thebarrier membrane 8, various formats are conceivable such as vertical partitioning, lateral partitioning, and concentric partitioning, but the following is a description of the case where the interior of theelectrolytic treatment container 4 is vertically partitioned by thebarrier membrane 8. - A positive electrode (anode) 9 is provided along the upper wall surface of the
electrolytic treatment container 4, a negative electrode (cathode) 11 is provided along the lower wall surface, and the anode 9 and thecathode 11 are respectively connected to a positive pole and negative pole of a power-supply unit 12. Accordingly, an anode-side region 9 a and cathode-side region 11 a are formed within theelectrolytic treatment container 4 by partitioning of the interior of theelectrolytic treatment container 4 by thebarrier membrane 8. - The power source of the power-
supply unit 12 is optional, but a power supply source utilizing natural energy such as photovoltaic power generation, wind power generation, wave power generation, ocean thermal power generation, and solar thermal power generation, or a fuel cell which has harmless emissions are preferable. A composite device composed of two or more power sources such as photovoltaic power generation, wind power generation, wave power generation, ocean thermal power generation, solar thermal power generation, and a fuel cell may also be used. Furthermore, in the case where power is supplied from an electric power plant, it is also acceptable to utilize nighttime surplus power. - As the anode 9, an anode is used in which a soluble metal is inputted as a
consumable electrode material 13 into a bucket (consumable electrode storage container) of reticular or porous plates of an insoluble metal such as titanium. Iron is preferable as the inputtedconsumable electrode material 13. Not only is iron easy to obtain as waste material, but the ferric ions that dissolve serve as nutrients for propagation of phytoplankton. As a result, phytoplankton is propagated by supplying ferric ions to the seawater, and carbon dioxide gas fixation by phytoplankton can also be anticipated. - The
cathode 11 uses platinized titanium or the like. Ahydrogen recovery device 14 is provided in the vicinity of thecathode 11 or opposite thecathode 11, and thehydrogen recovery device 14 recovers hydrogen gas generated on thecathode 11 side. Seawater (anodicelectrolyzed water 7 a) that flows through the anode 9 side (anode-side region 9 a) is directed to thefirst treatment tank 2, and seawater (cathodicelectrolyzed water 7 b) that flows through thecathode 11 side (cathode-side region 11 a) is directed to thesecond treatment tank 3. - The
first treatment tank 2 has a wasteconcrete input device 15, and concrete that is waste material is inputted into thefirst treatment tank 2 by the wasteconcrete input device 15. The inputted waste concrete is preferably pulverized with a large surface area, and removal of aggregate such as sand, rocks and the like is more preferable. Hydrogen gas recovered in theseawater 7 is supplied as a reducing agent of the fuel cell to thesecond treatment tank 3. Precipitated Mg(OH)2 is deposited in thesecond treatment tank 3, and the deposited Mg(OH)2 is recovered. The anodicelectrolyzed water 7 a that flows out from thefirst treatment tank 2 and the cathodicelectrolyzed water 7 b that flows out from thesecond treatment tank 3 are intermixed, and discharged to the ocean after adjustment of pH. - The operations of the present embodiment are described below.
- Electrolysis of seawater occurs by applying voltage between the anode 9 and the
cathode 11 to cause energization between the anode 9 andcathode 11, and it is primarily the reactions of the following formulas (1) and (2) that occur on thecathode 11 side. -
H2+1/2O2+2e− →2OH − (1) -
2H2O+2e−→2OH−+H2 (2) - Accordingly, the pH of seawater on the cathode side (cathodic
electrolyzed water 7 b) increases due to generation of OH− (hydroxy ions), producing CaCO3 and Mg(OH)2, as shown inFIG. 2 . In addition, when current-carrying volume per unit area of thecathode 11 is considered as cathode current density Dk (A/m2), the cathode current density Dk and the precipitation ratio of CaCO3 and Mg(OH)2 are as shown inFIG. 2 . That is, when the cathode current density Dk increases, the precipitation ratio of Mg(OH)2 increases, and a saturated condition ensues with respect to precipitation of Mg(OH)2 at the point where cathode current density Dk exceeds 2 (A/m2). Precipitation of CaCO3 gradually decreases and precipitation of Mg(OH)2 gradually increases up to a cathode current density Dk of 2 (A/m2). Consequently, by controlling the cathode current density Dk, it becomes possible to control the precipitation ratio of CaCO3 and Mg(OH)2, or to selectively precipitate CaCO3 and Mg(OH)2. - Therefore, by conducting electrolysis with cathode current density Dk set high—that is, by conducting electrolysis of seawater at a cathode current density Dk of 2 [A/m2] or higher in accordance with FIG. 2—it is possible to have most of the precipitate be Mg(OH)2.
- The cathodic
electrolyzed water 7 b is stored in thesecond treatment tank 3 in a state where Mg(OH)2 has precipitated. The precipitated Mg(OH)2 is deposited in thesecond treatment tank 3, and the precipitate is recovered by a precipitate recovery means 16. - In the aforementioned seawater electrolysis process, oxygen gas is generated on the anode 9 side, and hydrogen gas is generated on the
cathode 11 side. The generated hydrogen gas is recovered by thehydrogen recovery device 14, and is supplied to the fuel cell as a reducing agent in the case where a fuel cell is used in the power-supply unit 12. - Next, in the case where iron is used as the
consumable electrode material 13 on the anode 9 side, the following reactions occur, dissolving the iron. Furthermore, ferrous hydroxide occurs and H+ is produced by hydrolysis of ferric ions, thereby lowering the pH of seawater on the anode 9 side (anodicelectrolyzed water 7 a). -
Fe→Fe2++2e− (3) -
Fe2++2H2O→Fe(OH)2+2H+ (4) - The anodic
electrolyzed water 7 a which flows into thefirst treatment tank 2 is turned acidic by 2H+. When waste concrete (Ca(OH)2) is inputted into thefirst treatment tank 2, the acidic seawater is neutralized by the waste concrete according to the following formula. -
Ca(OH)2+2H+→Ca2++2H2O (5) - In the case where an insoluble metal is used in the anode 9, or when seawater electrolysis is conducted at a high current density, chlorine Cl2 is generated, and HCl and HClO are generated in conjunction with the generation of Cl2. As HCl is strongly acidic, and as HClO is a harmful substance to living creatures, electrolysis is conducted at a current density that inhibits generation of HCl and HClO to the utmost. However, as stated above, waste concrete (Ca(OH)2) is inputted into the anodic
electrolyzed water 7 a, whereby the HCl is neutralized by the reaction of: -
Ca(OH)2+HCl→+CaCl2+2H2O (6) - The seawater that has been neutralized and treated in the
first treatment tank 2 is then intermixed with the seawater discharged from thesecond treatment tank 3, and released into the ocean. In this case, the pH of the seawater after intermixture is adjusted to 8.0—that is, to a pH identical to that of seawater—by controlling the amount of concrete to be dissolved in the anodicelectrolyzed water 7 a and the amount of carbon dioxide gas to be blown into the cathodicelectrolyzed water 7 b. - Therefore, according to the present invention, as recovery of Mg(OH)2 can be continuously conducted, and as waste concrete is used in the fixation treatment process, treatment of industrial waste material can be conducted in parallel. Furthermore, as the seawater that is discharged after recovery of Mg(OH)2 has a pH identical to that of natural seawater, there is no environmental impact. As the ferric ions dissolved in the electrolytic process cause propagation of phytoplankton, fixation of carbon dioxide gas is also promoted.
- As stated above, in the seawater electrolysis process, oxygen gas is generated on the anode 9 side, and hydrogen gas is generated on the
cathode 11 side. In the case where a fuel cell is used in the power-supply unit 12, the oxygen gas and the hydrogen gas are supplied to the fuel cell, serving as fuel for power generation. - Next, an example of material balance in the foregoing embodiment is described with reference to
FIG. 3 . InFIG. 3 , components identical to those shown inFIG. 1 are given the same reference symbols. - Electrolytic reaction is varied by varying the cathode current density Dk, and electrolytic reaction is promoted by increasing the cathode current density Dk. Therefore, it is possible to control pH on the anode 9 side and the
cathode 11 side in the Mg(OH)2 recovery treatment process by controlling the cathode current density Dk. - First, the pH of the cathodic
electrolyzed water 7 b is set to 10-11, and Ca2+and Mg2+in the seawater are entirely precipitated by electrolysis. At this time, the pH of the anodicelectrolyzed water 7 a is on the order of 3-4. In order to conduct recovery of Mg(OH)2 efficiently, the cathode current density Dk is set to 2 [A/m2] or higher. - Recovery of the Mg(OH)2 that has precipitated in the
second treatment tank 3 is then conducted. The pH of the cathodicelectrolyzed water 7 b that flows out from thesecond treatment tank 3 is set to 10-11. Waste concrete is inputted into thefirst treatment tank 2, and the pH of the anodicelectrolyzed water 7 a that flows out from thefirst treatment tank 2 is adjusted to 4-5. The pH of the outflowing anodicelectrolyzed water 7 a is but one example, and the input amount of the aforementioned waste concrete is adjusted so that pH is 8.0-8.2 when the anodicelectrolyzed water 7 a and the cathodicelectrolyzed water 7 b are intermixed. By setting the pH of the discharged wastewater to 8.0-8.2, recovery of Mg(OH)2 can be conducted while discharging wastewater without changing the physical properties of the seawater. Accordingly, there is no impact on the environment. - By refining the recovered Mg(OH)2, magnesium metal can be produced.
- In the foregoing embodiment, waste concrete is used as the neutralizer of the anodic
electrolyzed water 7 a, but any neutralizer is acceptable provided that it is waste material having alkalinity, such as the coal ash produced in thermoelectric power plants. - In the foregoing embodiment, seawater electrolysis is conducted while circulating seawater inside the
electrolysis tank 1, but it is also acceptable to have a batch system in which on-off valves are respectively provided in theinlet 5 and theoutlet 6, seawater electrolysis is conducted in a state where theinlet 5 and theoutlet 6 are closed, and the seawater inside theelectrolysis tank 1 is replaced after electrolytic treatment. -
FIG. 4 shows an overview of a Mg(OH)2 recovery apparatus pertaining to an embodiment of the present invention. - In
FIG. 4 , components identical to those shown inFIG. 1 are given the same reference symbols. Moreover, in the embodiment shown inFIG. 4 , afuel cell 18 is shown as the power source. - In this apparatus, a hydrogen
gas recovery line 21 is provided which recovers hydrogen gas that is generated on thehydrogen recovery device 14 side of theelectrolysis tank 1, and which supplies it to thefuel cell 18, and an oxygengas recovery line 22 is provided which recovers oxygen gas that is generated on the anode 9 side of theelectrolysis tank 1, and which supplies it to thefuel cell 18. The hydrogengas recovery line 21 and the oxygengas recovery line 22 respectively have gas flow-rate regulation blowers fuel cell 18. - The power generated by the
fuel cell 18 accumulates in the power-supply unit 12, and the supply of accumulated power is controlled so that a prescribed cathode current density Dk is attained in thecathode 11. Power shortfalls in the amount of power generated by thefuel cell 18 are supplemented by power from photovoltaic power generation, wind power generation, or wave power generation, or by power from electric power plants. - A
seawater supply line 25, a waste concrete tank 26 (equivalent to the first treatment tank 2), and a recovery tank 27 (equivalent to the second treatment tank 3) are connected to theelectrolysis tank 1. - Acidic water which is the anodic
electrolyzed water 7 a is supplied to thewaste concrete tank 26, waste concrete is inputted into thewaste concrete tank 26, pH is adjusted so that the water is weakly acidic, and the adjusted water is discharged. - Alkaline water which is the cathodic
electrolyzed water 7 b containing Mg(OH)2 is supplied to therecovery tank 27. The Mg(OH)2 that has precipitated in therecovery tank 27 is recovered, and the cathodicelectrolyzed water 7 b (alkaline water) from which Mg(OH)2 has been removed is discharged from therecovery tank 27. - After the acidic water that has been discharged from the
waste concrete tank 26 and the alkaline water that has been discharged from therecovery tank 27 are intermixed, discharge is conducted from the recovery apparatus into the ocean. The pH of the wastewater is adjusted by the intermixing of acidic water and alkaline water, with the result that the pH of the wastewater in a state where it is finally released from the recovery apparatus is identical to the pH of seawater, and there is no impact on the environment. - In
FIG. 4 , 31 indicates a pump which feeds seawater to theelectrolysis tank electrolyzed water 7 b to therecovery tank waste concrete tank recovery tank 27. - According to the present invention, it is possible to provide a magnesium recovery method and a magnesium recovery apparatus which enable recovery of magnesium from seawater while minimizing impact on the environment.
- 1: electrolysis tank,
- 2: first treatment tank,
- 3: second treatment tank,
- 4: electrolytic treatment container,
- 5: inlet,
- 7: seawater,
- 7 a: anodic electrolyzed water,
- 7 b: cathodic electrolyzed water,
- 8: barrier film,
- 9: anode,
- 9 a: anode-side region,
- 11: cathode,
- 11 a: cathode-side region,
- 12: power-supply unit,
- 13: consumable electrode material,
- 14: hydrogen recovery device,
- 15: waste concrete input device,
- 16: carbon dioxide gas blower,
- 18: fuel cell,
- 21: hydrogen gas recovery line,
- 22: oxygen gas recovery line,
- 26: waste concrete tank,
- 27: recovery tank
Claims (8)
1. A magnesium recovery method comprising:
electrolyzing seawater;
separating anodic electrolyzed water and cathodic electrolyzed water produced by electrolysis of the seawater;
inputting alkaline material into the anodic electrolyzed water to adjust pH;
precipitating magnesium as magnesium hydroxide in the cathodic electrolyzed water, and recovering the magnesium hydroxide; and
intermixing the anodic electrolyzed water after pH adjustment and the cathodic electrolyzed water after recovery of the magnesium hydroxide, and discharging the intermixed water in a state where a pH of the intermixed water is identical to a pH of the seawater.
2. The magnesium recovery method according to claim 1 , wherein the alkaline material is waste concrete.
3. The magnesium recovery method according to claim 1 , wherein iron, which is a soluble metal, is used in the anode-side electrode to cause dissolution of ferric ions in the anodic electrolyzed water in the seawater electrolysis process.
4. A magnesium recovery apparatus, comprising:
an electrolysis tank having an anode and a cathode;
a barrier film which partitions an interior of the electrolysis tank into an anode-side region containing the anode, and a cathode-side region containing the cathode;
a first treatment tank which stores anodic electrolyzed water produced in the anode-side region;
a second treatment tank which stores cathodic electrolyzed water produced in the cathode-side region;
a power-supply unit which supplies power to the anode and the cathode;
an alkaline material input device which inputs alkaline material to the first treatment tank; and
a recovery unit which recovers magnesium hydroxide precipitated in the second treatment tank,
wherein wastewater from the first treatment tank and wastewater from the second treatment tank are intermixed, and discharged in a state where a pH of the intermixed water is identical to a pH of seawater.
5. The magnesium recovery apparatus according to claim 4 , wherein the power-supply unit has at least one of photovoltaic cell, fuel cell, wind power generator, wave power generator, ocean thermal power generator, and solar thermal power generator.
6. The magnesium recovery apparatus according to claim 4 , wherein the power-supply unit contains a fuel cell which uses hydrogen gas generated on the cathode-side region, and oxygen gas generated on the anode-side region.
7. The magnesium recovery apparatus according to claim 4 , wherein the alkaline material inputted from the alkaline material input device is waste concrete.
8. The magnesium recovery apparatus according to claim 4 , wherein the anode contains iron as a consumable electrode, and the consumable electrode dissolves ferric ions.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2010203353A JP5824793B2 (en) | 2010-09-10 | 2010-09-10 | Magnesium recovery method and magnesium recovery device |
JP2010-203353 | 2010-09-10 | ||
PCT/JP2011/070236 WO2012033083A1 (en) | 2010-09-10 | 2011-09-06 | Magnesium recovery method and magnesium recovery apparatus |
Publications (1)
Publication Number | Publication Date |
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US20130161200A1 true US20130161200A1 (en) | 2013-06-27 |
Family
ID=45810681
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US13/820,630 Abandoned US20130161200A1 (en) | 2010-09-10 | 2011-09-06 | Magnesium recovery method and magnesium recovery apparatus |
Country Status (8)
Country | Link |
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US (1) | US20130161200A1 (en) |
JP (1) | JP5824793B2 (en) |
AU (1) | AU2011299918B2 (en) |
CA (1) | CA2810648C (en) |
GB (1) | GB2497256A (en) |
NO (1) | NO20130459A1 (en) |
SG (1) | SG188458A1 (en) |
WO (1) | WO2012033083A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9499880B2 (en) | 2015-03-06 | 2016-11-22 | Battelle Memorial Institute | System and process for production of magnesium metal and magnesium hydride from magnesium-containing salts and brines |
CN107164777A (en) * | 2017-05-12 | 2017-09-15 | 中国科学院过程工程研究所 | A kind of method of film electrolysis separating magnesium and enriching lithium from salt lake brine with high magnesium-lithium ratio |
US10968126B2 (en) | 2017-07-07 | 2021-04-06 | Katz Water Tech, Llc | Pretreatment of produced water to facilitate improved metal extraction |
US11305228B2 (en) | 2019-08-29 | 2022-04-19 | Kenji SORIMACHI | Method for fixing carbon dioxide, method for producing fixed carbon dioxide, and fixed carbon dioxide production apparatus |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101710283B1 (en) * | 2015-11-11 | 2017-03-08 | 고려대학교 산학협력단 | Highly selective magnesium recovery apparatus and Highly selective magnesium recovery method using thereof |
JP7008305B2 (en) * | 2020-01-22 | 2022-01-25 | 健司 反町 | How to fix carbon dioxide and how to make fixed carbon dioxide |
CN113439071A (en) * | 2020-01-22 | 2021-09-24 | 反町健司 | Method for fixing carbon dioxide, method for producing fixed carbon dioxide, and device for fixing carbon dioxide |
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JP2005262158A (en) * | 2004-03-22 | 2005-09-29 | Shimizu Corp | Concrete regenerated fine powder and neutralization method |
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-
2010
- 2010-09-10 JP JP2010203353A patent/JP5824793B2/en active Active
-
2011
- 2011-09-06 CA CA2810648A patent/CA2810648C/en not_active Expired - Fee Related
- 2011-09-06 WO PCT/JP2011/070236 patent/WO2012033083A1/en active Application Filing
- 2011-09-06 GB GB1306089.2A patent/GB2497256A/en not_active Withdrawn
- 2011-09-06 AU AU2011299918A patent/AU2011299918B2/en not_active Ceased
- 2011-09-06 SG SG2013017231A patent/SG188458A1/en unknown
- 2011-09-06 US US13/820,630 patent/US20130161200A1/en not_active Abandoned
-
2013
- 2013-04-05 NO NO20130459A patent/NO20130459A1/en not_active Application Discontinuation
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US6190530B1 (en) * | 1999-04-12 | 2001-02-20 | International Business Machines Corporation | Anode container, electroplating system, method and plated object |
US6375825B1 (en) * | 1999-10-28 | 2002-04-23 | Chemical Products Corporation | Process for the production of alkaline earth hydroxide |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US9499880B2 (en) | 2015-03-06 | 2016-11-22 | Battelle Memorial Institute | System and process for production of magnesium metal and magnesium hydride from magnesium-containing salts and brines |
CN107164777A (en) * | 2017-05-12 | 2017-09-15 | 中国科学院过程工程研究所 | A kind of method of film electrolysis separating magnesium and enriching lithium from salt lake brine with high magnesium-lithium ratio |
CN107164777B (en) * | 2017-05-12 | 2019-01-25 | 中国科学院过程工程研究所 | A kind of method of film electrolysis separating magnesium and enriching lithium from salt lake brine with high magnesium-lithium ratio |
US10968126B2 (en) | 2017-07-07 | 2021-04-06 | Katz Water Tech, Llc | Pretreatment of produced water to facilitate improved metal extraction |
US11685676B2 (en) | 2017-07-07 | 2023-06-27 | Katz Water Tech, Llc | Pretreatment of produced water to facilitate improved metal extraction |
US11305228B2 (en) | 2019-08-29 | 2022-04-19 | Kenji SORIMACHI | Method for fixing carbon dioxide, method for producing fixed carbon dioxide, and fixed carbon dioxide production apparatus |
Also Published As
Publication number | Publication date |
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JP2012057230A (en) | 2012-03-22 |
AU2011299918A1 (en) | 2013-05-02 |
CA2810648A1 (en) | 2012-03-15 |
AU2011299918B2 (en) | 2014-09-04 |
GB2497256A (en) | 2013-06-05 |
SG188458A1 (en) | 2013-04-30 |
GB201306089D0 (en) | 2013-05-22 |
NO20130459A1 (en) | 2013-04-16 |
JP5824793B2 (en) | 2015-12-02 |
CA2810648C (en) | 2016-01-12 |
WO2012033083A1 (en) | 2012-03-15 |
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