US20130037416A1 - Method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide - Google Patents
Method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide Download PDFInfo
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- US20130037416A1 US20130037416A1 US13/521,952 US201113521952A US2013037416A1 US 20130037416 A1 US20130037416 A1 US 20130037416A1 US 201113521952 A US201113521952 A US 201113521952A US 2013037416 A1 US2013037416 A1 US 2013037416A1
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- manganese
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- manganese dioxide
- leaching
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- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 title claims abstract description 90
- 229910052748 manganese Inorganic materials 0.000 title claims abstract description 41
- 239000011572 manganese Substances 0.000 title claims abstract description 41
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 22
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 claims abstract description 50
- 238000002386 leaching Methods 0.000 claims abstract description 50
- 238000000034 method Methods 0.000 claims abstract description 31
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 28
- 229940099596 manganese sulfate Drugs 0.000 claims abstract description 25
- 239000011702 manganese sulphate Substances 0.000 claims abstract description 25
- 235000007079 manganese sulphate Nutrition 0.000 claims abstract description 25
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 claims abstract description 25
- 238000000746 purification Methods 0.000 claims abstract description 22
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000011575 calcium Substances 0.000 claims abstract description 21
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 21
- 239000000843 powder Substances 0.000 claims abstract description 21
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 19
- 238000005868 electrolysis reaction Methods 0.000 claims abstract description 19
- 238000002156 mixing Methods 0.000 claims abstract description 19
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000011777 magnesium Substances 0.000 claims abstract description 15
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 15
- 239000012535 impurity Substances 0.000 claims abstract description 14
- 229910052683 pyrite Inorganic materials 0.000 claims abstract description 11
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000011028 pyrite Substances 0.000 claims abstract description 11
- 229910052742 iron Inorganic materials 0.000 claims abstract description 10
- 238000006243 chemical reaction Methods 0.000 claims abstract description 7
- 235000008733 Citrus aurantifolia Nutrition 0.000 claims abstract description 6
- 235000011941 Tilia x europaea Nutrition 0.000 claims abstract description 6
- 239000004088 foaming agent Substances 0.000 claims abstract description 6
- 239000004571 lime Substances 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims abstract description 6
- 229920001021 polysulfide Polymers 0.000 claims abstract description 6
- 239000005077 polysulfide Substances 0.000 claims abstract description 6
- 150000008117 polysulfides Polymers 0.000 claims abstract description 6
- 239000000375 suspending agent Substances 0.000 claims abstract description 6
- 229910001414 potassium ion Inorganic materials 0.000 claims abstract description 3
- 238000010438 heat treatment Methods 0.000 claims abstract 2
- 239000000047 product Substances 0.000 claims description 22
- 238000005406 washing Methods 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000002245 particle Substances 0.000 claims description 12
- 238000006386 neutralization reaction Methods 0.000 claims description 10
- 239000003792 electrolyte Substances 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 8
- 239000003518 caustics Substances 0.000 claims description 6
- 230000032683 aging Effects 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 5
- 230000005484 gravity Effects 0.000 claims description 5
- 238000000265 homogenisation Methods 0.000 claims description 5
- 239000002244 precipitate Substances 0.000 claims description 5
- 238000000108 ultra-filtration Methods 0.000 claims description 5
- 239000002699 waste material Substances 0.000 claims description 4
- 238000003801 milling Methods 0.000 claims description 2
- 230000008901 benefit Effects 0.000 abstract description 5
- 238000001914 filtration Methods 0.000 abstract description 4
- 230000007935 neutral effect Effects 0.000 abstract description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 14
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 239000002994 raw material Substances 0.000 description 6
- 239000011133 lead Substances 0.000 description 5
- 239000010949 copper Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000010941 cobalt Substances 0.000 description 3
- 229910017052 cobalt Inorganic materials 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 229910001385 heavy metal Inorganic materials 0.000 description 3
- 239000011344 liquid material Substances 0.000 description 3
- 239000011656 manganese carbonate Substances 0.000 description 3
- 235000006748 manganese carbonate Nutrition 0.000 description 3
- 229940093474 manganese carbonate Drugs 0.000 description 3
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 3
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 238000003723 Smelting Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/04—Extraction of metal compounds from ores or concentrates by wet processes by leaching
- C22B3/06—Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic acid solutions, e.g. with acids generated in situ; in inorganic salt solutions other than ammonium salt solutions
- C22B3/08—Sulfuric acid, other sulfurated acids or salts thereof
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/44—Treatment or purification of solutions, e.g. obtained by leaching by chemical processes
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B47/00—Obtaining manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B47/00—Obtaining manganese
- C22B47/0018—Treating ocean floor nodules
- C22B47/0045—Treating ocean floor nodules by wet processes
- C22B47/0081—Treatment or purification of solutions, e.g. obtained by leaching
-
- 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
- C25B1/21—Manganese oxides
-
- 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
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
Definitions
- the present invention claims the benefit of the priority of the Chinese Application titled “METHOD FOR PRODUCING MERCURY-FREE ALKALINE-MANGANESE TYPE ELECTROLYZED MANGANESE DIOXIDE”, whose Application No. is 201010227988.7 and Application Date is 15, Jul., 2 010, and whole of which can be combined into the present invention.
- the present invention involves a method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide; especially involves a method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide by leaching ultra-low-grade manganese oxide minerals by “two-ores method”.
- alkaline-manganese batteries As the high power battery of the lowest cost-performance ratio in battery industry, alkaline-manganese batteries have features such as steady working voltage, continuous discharge of large current, good performance, long storage time (up to 3-5 years), excellent low temperature performance and leak-proof performance and so on, and are popular both home and abroad.
- the annual consumption of the mercury-free alkaline-manganese type electrolyzed manganese dioxide, which is the main material for producing alkaline-manganese batteries, is more than 300000 tons, and is increasing by more than 10% every year. So it has a bright market prospects.
- the main raw material is manganese carbonate ore or manganese oxide ore.
- the content of the manganese carbonate in the ore is low (below 30%), a large consumption of manganese ore and a high cost of products are resulted.
- the recently main processes comprise the leaching solution after reducing the manganese oxide ore by roasting and “two-ores method” to produce the electrolyzed manganese dioxide, wherein, the method of the leaching solution after reducing roasting manganese oxide ore by roasting has the shortcomings such as long process flow, high production cost, and easily causing pollution to the surrounding environment of the factory; and the “two-ores method” with high grade manganese oxide as raw material to produce the electrolyzed manganese dioxide, i.e. leaching solution of the manganese dioxide ore and the pyrites which is the reducing agent, when using the low-grade manganese ore, i.e.
- the grade of it is lower than 25%, has the shortcomings such as low leaching rate, long turnaround time of material among the devices, the increased amount of equipments and low utilization rate because of using intermittent leaching process in the domestic manganese metallurgical industry recently, i.e. directly dissolving the manganese ore into solution in one sole leaching tank
- the increasingly reducing of the used high-grade manganese ore resources will lead to a difficulty of the method to maintain long-term production.
- the manganese ore resource in Guangxi province is rich, but most of which are low-grade manganese ore characterized by low manganese content, high impurity content, so it wasn't adequately exploited for a long time.
- the technical problems to be solved by the invention is to provide a method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide by “two-ores method”, with ultra-low-grade manganese oxide ore as main raw material.
- the technical scheme of the invention for solving the technical problems is to provide a method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide, which comprises the sequential steps: (1) mixing manganese oxide ore and pyrite, continuously feeding the mixture and sulfuric acid into a continuous leaching tank composed of 1-7 stirring leaching tanks to form a one-stage or multi-stage continuous leaching, controlling the reaction temperature at 90-95° C. for about 3 to 4 hours during the process, removing potassium ions first after the leaching, and then removing iron by means of a neutral iron removal method, and adding lime powder at the late stage of iron removal to adjust the pH value of the solution to 6-6.5 at 90-95° C.
- electrolysis conditions electrolyte temperature is 100-103° C., the anodic current density is 80-85 A/m 2 , the cell voltage is 2.2-3.5V, electrolytic period is 12-20 days, after electrolysis the mercury-free alkaline-manganese type electrolyzed manganese dioxide is obtained.
- step 1 directly feeding the manganese oxide ore and pyrite into the continuous leaching tank by the ratio of 1:0.24, at the same time blending sulfuric acid and waste electrolyte by the ratio of ore to acid of 1:0.47.
- the said waste electrolyte come from the raffinate generated during the electrolysis in the step 3.
- step 3 broking the crude electrolyzed manganese dioxide products obtained from electrolysis on the anode into 6-8 mm particles, entering the particles into a washing rank, using the three-rinsing process which contains washing by water, caustic washing, and washing by water, wherein, the temperature of the alkali liquor for the first and the second caustic washing are both 60-70° C., the temperature of the water for the last washing is 80-90° C., and the rinsing period is 40 hours.
- the rinsing liquids are heated directly by steam. And then the electrolyzed manganese dioxide with required particle size is obtained through milling.
- the present invention has the following beneficial effects: the method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide provide by the present reduce the grade of the used manganese oxide to its 16% by using the ultra-low-grade manganese oxide ore as main raw material, directly leaching the manganese from the ultra-low-grade manganese oxide ore by “two-ores method”, performing deep purification to remove the impurities from the obtained manganese sulfate solution, and then performing electrolysis to produce mercury-free alkaline-manganese type electrolyzed manganese dioxide.
- the process used is not only adaptable for the low-grade and complicated manganese oxide ore, but also adaptable for the high-grade manganese oxide ore, therefore, it has the advantages such as wide adaptability to manganese oxide ores, short process flow, low production cost and so on. It can make full use of the large quantity of low-grade manganese ore in Guangxi Province to produce mercury-free electrolyzed manganese dioxide product, so that it has a very good economic benefits and social benefits to the rational use of manganese ore resources, reduce the production cost.
- Figure 1 is the flow diagram of the process of the embodiment of the invention.
- the continuous leaching tank is composed of one leaching tank for one-stage continuous leaching, wherein, the effective volume of the leaching tank is 1 m 3 , and the temperature of the tank is 95° C.
- the reaction time of leaching from feeding to out of the leaching tank is 3 hours until the pH values is to 3-3.5 that indicates that the leaching reaction has been completed. Continuously stir during the reaction.
- the liquid material flowing from the leaching tank enters the neutralization tank in series, the effective volume of which is 1.5 m 3 . Adding lime powder to continuously perform neutralization reaction, with controlled pH value of 6.0 for 3 hours. After the neutralization, carrying out filtering and the delivering the filter residue to the residue site, and the crude manganese sulfate solution which contains heavy metals such as copper, cobalt, nickel, lead and impurities such as calcium, magnesium is obtained.
- the filter residue is sent to residue site, and then performing the second stage of purification, wherein the solution passes through a sluice first so that the calcium and magnesium are dynamically removed, and then the solution is sent to a standing tank and left it for 32 hours to ageing the solution and remove impurities such as calcium and magnesium as precipitate, to obtain refined manganese sulfate solution.
- the filter residue is sent to residue site, and delivering the filtrate to electrolysis.
- the qualified refined manganese sulfate solution to ultra filtration, to heat to 90° C. by a plate heat exchanger, and then to suspension electrolysis by entering an elevated tank. And the prepared suspending agent and foaming agent are added at the same time.
- the electrolyte temperature is 100° C.
- the anodic current density is 81 A/m 2
- the cell voltage is 2.4 V
- electrolytic period is 12 days. Stripping the crude products of manganese dioxide on the anode, and broking them to particles of 6-8 mm by crusher, then delivering them into rinse ranks, and the effective volume of each rinse rank is 1 m 3 .
- the temperature of the alkali liquor of the first and the second rinsing are both 60° C.
- the temperature of the water of the last rinsing is 80° C.
- the rinse period is 40 hours.
- the rinsing liquids are directly heated by steam. Sending the rinsed electrolyzed manganese dioxide into pendulum grinder, to grind and collecting the powder product (particle size is ⁇ 325 mesh).
- the continuous leaching tank is composed of three leaching tanks for three-stage continuous leaching during which material liquid enters the third leaching tank after out of the second leaching tank, wherein, the effective volume of each leaching tank is 1 m 3 , and the temperature of each tank is 93° C.
- the reaction time of leaching from feeding to out of the third leaching tank is 3.5 hours. Continuously stir during the reaction.
- the liquid material flowing from the third leaching tank enters the neutralization tank in series, the effective volume of which is 1.5 m 3 . Adding lime powder to continuous perform neutralization reaction, with controlled pH value of 6.3 for 3.5 hours. After the neutralization, carrying out filtering and delivering the filter residue to the residue site, and the crude manganese sulfate solution which contains heavy metals such as copper, cobalt, nickel, lead and impurities such as calcium, magnesium is obtained.
- the filter residue is sent to residue site, and then performing the second stage of purification, wherein the solution passes through a sluice first so that the calcium and magnesium are dynamically removed, and then the solution is sent to a standing tank and left it for 32 hours to ageing the solution and remove impurities such as calcium and magnesium as precipitate, to obtain refined manganese sulfate solution.
- the filter residue is sent to residue site, and delivering the filtrate to electrolysis.
- the qualified refined manganese sulfate solution to ultra filtration, to heat to 95° C. by a plate heat exchanger, and then to suspension electrolysis by entering an elevated tank. And the prepared suspending agent and foaming agent are added at the same time.
- the electrolyte temperature is 102° C.
- the anodic current density is 83 A/m 2
- the cell voltage is 2.9 V
- electrolytic period is 15 days. Stripping the crude products of manganese dioxide on the anode, and broking them to particles of 6-8 mm by crusher, then delivering them into rinse ranks, and the effective volume of each rinse rank is 1 m 3 .
- the temperature of the alkali liquor of the first and the second rinsing are both 65° C.
- the temperature of the water of the last rinsing is 85° C.
- the rinse period is 40 hours.
- the rinsing liquids are directly heated by steam. Sending the rinsed electrolyzed manganese dioxide into pendulum grinder, to grind and collecting the powder product (particle size is ⁇ 325 mesh).
- the continuous leaching tank is composed of seven leaching tanks for seven-stage continuous leaching during which material liquid enters the third to the seventh leaching tank after out of the second leaching tank, wherein, the effective volume of each leaching tank is 1 m 3 , and the temperature of each tank is 95° C.
- the reaction time of leaching from feeding to out of the seventh leaching tank is 4 hours. Continuously stir during the reaction.
- the liquid material flowing from the seventh leaching tank enters the neutralization tank in series, the effective volume of which is 1.5 m 3 .
- the filter residue is sent to residue site, and then performing the second stage of purification, wherein the solution passes through a sluice first so that the calcium and magnesium are dynamically removed, and then the solution is sent to a standing tank and left it for 32 hours to ageing the solution and remove impurities such as calcium and magnesium as precipitate, to obtain refined manganese sulfate solution.
- the filter residue is sent to residue site, and delivering the filtrate to electrolysis
- the qualified refined manganese sulfate solution to ultra filtration, to heat to 100° C. by a plate heat exchanger, and then to suspension electrolysis by entering an elevated tank. And the prepared suspending agent and foaming agent are added at the same time.
- the electrolyte temperature is 103° C.
- the anodic current density is 85 A/m 2
- the cell voltage is 3.5 V
- electrolytic period is 20 days. Stripping the crude products of manganese dioxide on the anode, and broking them to particles of 6-8 mm by crusher, then delivering them into rinse ranks, and the effective volume of each rinse rank is 1 m 3 .
- the temperature of the alkali liquor of the first and the second rinsing are both 70° C.
- the temperature of the water of the last rinsing is 85° C.
- the rinse period is 40 hours.
- the rinsing liquids are directly heated by steam. Sending the rinsed electrolyzed manganese dioxide into pendulum grinder, to grind and collecting the powder product (particle size is ⁇ 325 mesh).
- the main indexes of the manganese dioxide products in the three examples are: MnO 2 ⁇ 91.0%, Fe ⁇ 60 ppm, Cu ⁇ 5 ppm, Pb ⁇ 5 ppm, Ni ⁇ 5 ppm, Co ⁇ 5 ppm, Mo ⁇ 0.5 ppm, As ⁇ 0.5 ppm, Sb ⁇ 0.5 ppm, K ⁇ 200 ppm.
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- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
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- Environmental & Geological Engineering (AREA)
- Geochemistry & Mineralogy (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Ocean & Marine Engineering (AREA)
- Oceanography (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Inorganic Compounds Of Heavy Metals (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201010227988.7 | 2010-07-15 | ||
| CN2010102279887A CN101892384B (zh) | 2010-07-15 | 2010-07-15 | 无汞碱锰型电解二氧化锰的生产方法 |
| PCT/CN2011/077011 WO2012006935A1 (zh) | 2010-07-15 | 2011-07-09 | 无汞碱锰型电解二氧化锰的生产方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20130037416A1 true US20130037416A1 (en) | 2013-02-14 |
Family
ID=43101728
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US13/521,952 Abandoned US20130037416A1 (en) | 2010-07-15 | 2011-07-09 | Method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20130037416A1 (enExample) |
| JP (1) | JP5764207B2 (enExample) |
| CN (1) | CN101892384B (enExample) |
| WO (1) | WO2012006935A1 (enExample) |
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| CN115094441A (zh) * | 2022-07-14 | 2022-09-23 | 广西桂柳新材料股份有限公司 | 锂电池用电解二氧化锰的生产方法 |
| CN120519869A (zh) * | 2025-07-25 | 2025-08-22 | 湘潭电化科技股份有限公司 | 低品位氧化锰矿制备电解二氧化锰的方法、电解二氧化锰及其应用 |
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| US7666593B2 (en) | 2005-08-26 | 2010-02-23 | Helicos Biosciences Corporation | Single molecule sequencing of captured nucleic acids |
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| CN110127766A (zh) * | 2019-07-02 | 2019-08-16 | 贵州中伟资源循环产业发展有限公司 | 一种电池级硫酸锰溶液的制备工艺 |
| CN113215387A (zh) * | 2021-02-25 | 2021-08-06 | 宁夏天元锰材料研究院(有限公司) | 一种碳酸锰低温分解活化的方法及系统 |
| CN114481165A (zh) * | 2021-12-31 | 2022-05-13 | 广西大新汇元新能源科技有限责任公司 | 基于半氧化锰矿生产电解二氧化锰的方法 |
| CN114715945A (zh) * | 2022-05-31 | 2022-07-08 | 广西下田锰矿有限责任公司 | 一种高效率纯化硫酸锰溶液的方法 |
| CN115074753A (zh) * | 2022-07-14 | 2022-09-20 | 广西桂柳新材料股份有限公司 | 碱锰电池用电解二氧化锰后处理除杂方法 |
| CN115094441A (zh) * | 2022-07-14 | 2022-09-23 | 广西桂柳新材料股份有限公司 | 锂电池用电解二氧化锰的生产方法 |
| CN120519869A (zh) * | 2025-07-25 | 2025-08-22 | 湘潭电化科技股份有限公司 | 低品位氧化锰矿制备电解二氧化锰的方法、电解二氧化锰及其应用 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2013538936A (ja) | 2013-10-17 |
| CN101892384A (zh) | 2010-11-24 |
| CN101892384B (zh) | 2011-09-21 |
| JP5764207B2 (ja) | 2015-08-12 |
| WO2012006935A1 (zh) | 2012-01-19 |
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