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 PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
manganese
stage
solution
manganese dioxide
leaching
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/521,952
Other languages
English (en)
Inventor
Qizhi Chen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangxi Non-Ferrous Metals Group Huiyuanmengye Co Ltd
Guangxi Non Ferrous Metals Group Huiyuanmengye Co Ltd
Original Assignee
Guangxi Non Ferrous Metals Group Huiyuanmengye Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Guangxi Non Ferrous Metals Group Huiyuanmengye Co Ltd filed Critical Guangxi Non Ferrous Metals Group Huiyuanmengye Co Ltd
Assigned to Guangxi Non-Ferrous Metals Group Huiyuanmengye Co., Ltd. reassignment Guangxi Non-Ferrous Metals Group Huiyuanmengye Co., Ltd. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHEN, QIZHI
Publication of US20130037416A1 publication Critical patent/US20130037416A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/04Extraction of metal compounds from ores or concentrates by wet processes by leaching
    • C22B3/06Extraction 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
    • C22B3/08Sulfuric acid, other sulfurated acids or salts thereof
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/20Treatment or purification of solutions, e.g. obtained by leaching
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/20Treatment or purification of solutions, e.g. obtained by leaching
    • C22B3/44Treatment or purification of solutions, e.g. obtained by leaching by chemical processes
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B47/00Obtaining manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B47/00Obtaining manganese
    • C22B47/0018Treating ocean floor nodules
    • C22B47/0045Treating ocean floor nodules by wet processes
    • C22B47/0081Treatment or purification of solutions, e.g. obtained by leaching
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00Electrolytic production of inorganic compounds or non-metals
    • C25B1/01Products
    • C25B1/21Manganese oxides
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

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.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • 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)
  • Battery Electrode And Active Subsutance (AREA)
US13/521,952 2010-07-15 2011-07-09 Method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide Abandoned US20130037416A1 (en)

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)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7666593B2 (en) 2005-08-26 2010-02-23 Helicos Biosciences Corporation Single molecule sequencing of captured nucleic acids
CN101892384B (zh) * 2010-07-15 2011-09-21 广西有色金属集团汇元锰业有限公司 无汞碱锰型电解二氧化锰的生产方法
CN102560526B (zh) * 2011-12-23 2015-03-25 苏州大学 一种高功率电解二氧化锰的制备方法
CN103074490B (zh) * 2013-01-09 2014-03-12 广西有色金属集团汇元锰业有限公司 一种多矿法生产电解金属锰过程中的净化方法
CN103205772B (zh) * 2013-04-15 2015-07-08 广西有色金属集团汇元锰业有限公司 电解二氧化锰的生产方法
CN103560240B (zh) * 2013-11-07 2015-11-25 广西桂柳化工有限责任公司 无汞碱性电池专用电解二氧化锰制备方法
CN103643252B (zh) * 2013-12-05 2016-05-18 中信大锰矿业有限责任公司大新锰矿分公司 一种二氧化锰电解悬浮剂
CN103710541B (zh) * 2013-12-24 2015-12-30 柳州豪祥特科技有限公司 湿法生产电解二氧化锰的方法
KR101528507B1 (ko) 2015-01-13 2015-06-12 한국지질자원연구원 리튬계 전지로부터 코발트 및 망간의 동시 회수 방법
CN104928709B (zh) * 2015-06-24 2017-04-12 广西有色金属集团汇元锰业有限公司 二氧化锰的电解系统及其生产方法
CN106480471B (zh) * 2016-11-04 2018-05-22 柳州高新区欧亚自动化设备有限责任公司 EMD连续浸出工艺化合槽pH值控制装置及其控制方法
CN110143615A (zh) * 2019-06-19 2019-08-20 贵州红星发展大龙锰业有限责任公司 电解二氧化锰及电解二氧化锰深度除钾的方法
CN110747329B (zh) * 2019-11-26 2022-02-22 广西汇元锰业有限责任公司 基于蔗渣造纸白泥的电解二氧化锰生产方法
CN111620355A (zh) * 2020-06-03 2020-09-04 四川兴晟锂业有限责任公司 一种去除氢氧化钾溶液中钾离子的方法
CN112708753B (zh) * 2020-12-29 2023-05-12 武钢资源集团大冶铁矿有限公司 一种铁精矿深度脱硫处理方法及系统
CN114477521B (zh) * 2021-12-31 2024-05-28 广西大新汇元新能源科技有限责任公司 一种电解二氧化锰废水处理及锰的回收利用方法
CN115724470B (zh) * 2022-09-26 2024-05-07 广西科技师范学院 一种硫酸锰溶液的净化方法
CN120483260B (zh) * 2025-04-17 2025-11-14 广西埃索凯新材料科技有限公司 一种二氧化硫还原氧化锰矿制备高纯硫酸锰联产电池用二氧化锰的方法

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1874827A (en) * 1931-05-12 1932-08-30 Burgess Battery Co Production of manganese dioxide
US2424958A (en) * 1943-08-31 1947-08-05 Dorr Co Process of electrodepositing a manganese dioxide compound
US3900385A (en) * 1973-09-20 1975-08-19 Mitsui Mining & Smelting Co Method for continuous production of electrolytic manganese dioxide
US4364665A (en) * 1979-12-11 1982-12-21 Krupp Polysius Ag Storage and mixing silo for bulk material
US4549943A (en) * 1984-11-01 1985-10-29 Union Carbide Corporation Suspension bath and process for production of electrolytic manganese dioxide
US20020046955A1 (en) * 2000-09-01 2002-04-25 Tosoh Corporation Powder of electrolytic manganese dioxide and process for producing the same
US20030180612A1 (en) * 1999-08-05 2003-09-25 David Kilby High discharge electrolytic manganese dioxide and an electrode and alkaline cell incorporating the same
US20030192832A1 (en) * 2002-04-15 2003-10-16 Bowers Gregory S. Essentially insoluble heavy metal sulfide slurry for wastewater treatment
WO2009120384A2 (en) * 2008-03-28 2009-10-01 Siemens Water Technologies Corp. Hybrid aerobic and anaerobic wastewater and sludge treatment systems and methods

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3348912A (en) * 1963-09-23 1967-10-24 Utah Construction & Mining Co Method of preparing manganese sulfate from pyrite reduced manganese dioxide ores
JPS5121959B1 (enExample) * 1969-06-16 1976-07-06
JPS49197A (enExample) * 1972-04-21 1974-01-05
JPS5988324A (ja) * 1982-11-12 1984-05-22 Japan Metals & Chem Co Ltd 電解二酸化マンガン用硫酸マンガン溶液の精製法
JPS60103192A (ja) * 1983-11-09 1985-06-07 Japan Metals & Chem Co Ltd 電解槽内蓄積物の処理法
JPS60236458A (ja) * 1984-05-10 1985-11-25 Toshiba Battery Co Ltd 水銀無添加電池
JPS6244586A (ja) * 1985-08-20 1987-02-26 Toshiba Battery Co Ltd 電池用電解二酸化マンガンの製造方法
CN87102046A (zh) * 1987-06-23 1987-12-09 桂阳县电解锰厂 用二氧化锰矿制取硫酸锰溶液的方法
CN1027294C (zh) * 1991-06-04 1995-01-04 上海钢铁研究所 电解二氧化锰用的钛合金阳极
JP3493835B2 (ja) * 1995-10-16 2004-02-03 松下電器産業株式会社 二酸化マンガンの製造法及びそれを用いたアルカリ乾電池
JP4730488B2 (ja) * 2000-04-04 2011-07-20 東ソー株式会社 マンガン鉱石処理物の製造方法
JP3553541B2 (ja) * 2001-11-26 2004-08-11 三井金属鉱業株式会社 電池用正極活物質及び電解二酸化マンガンの製造方法並びに電池
CN1861815A (zh) * 2005-05-14 2006-11-15 广西汇元锰业有限公司 连续浸出氧化锰矿的方法
CN1907866A (zh) * 2005-08-01 2007-02-07 李忠红 锰矿石直接制备四氧化三锰的方法
CN101456594A (zh) * 2007-12-14 2009-06-17 杜祖德 利用低品位锰矿渣制取硫酸锰的方法
CN101684562A (zh) * 2008-09-28 2010-03-31 熊一言 氧化锰矿的制液工艺
CN101550556A (zh) * 2009-04-01 2009-10-07 广西靖西县一洲锰业有限公司 碱性锌锰电池用电解二氧化锰的制备方法
CN101892384B (zh) * 2010-07-15 2011-09-21 广西有色金属集团汇元锰业有限公司 无汞碱锰型电解二氧化锰的生产方法

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1874827A (en) * 1931-05-12 1932-08-30 Burgess Battery Co Production of manganese dioxide
US2424958A (en) * 1943-08-31 1947-08-05 Dorr Co Process of electrodepositing a manganese dioxide compound
US3900385A (en) * 1973-09-20 1975-08-19 Mitsui Mining & Smelting Co Method for continuous production of electrolytic manganese dioxide
US4364665A (en) * 1979-12-11 1982-12-21 Krupp Polysius Ag Storage and mixing silo for bulk material
US4549943A (en) * 1984-11-01 1985-10-29 Union Carbide Corporation Suspension bath and process for production of electrolytic manganese dioxide
US20030180612A1 (en) * 1999-08-05 2003-09-25 David Kilby High discharge electrolytic manganese dioxide and an electrode and alkaline cell incorporating the same
US20020046955A1 (en) * 2000-09-01 2002-04-25 Tosoh Corporation Powder of electrolytic manganese dioxide and process for producing the same
US20030192832A1 (en) * 2002-04-15 2003-10-16 Bowers Gregory S. Essentially insoluble heavy metal sulfide slurry for wastewater treatment
WO2009120384A2 (en) * 2008-03-28 2009-10-01 Siemens Water Technologies Corp. Hybrid aerobic and anaerobic wastewater and sludge treatment systems and methods

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
"Heating vats and tanks by steam injection." Spirax Sarco. 10 Feb 2010 capture of <http://www.spiraxsarco.com/resources/steam-engineering-tutorials/steam-engineering-principles-and-heat-transfer/heating-tanks-and-vats-by-steam-injection.asp> *
ChemGuide.co.uk. "The Effect of Temperature on Reaction Rates." 16 June 2010 capture of using Internet Archive Wayback Machine *
Smoot Division of Magnum Systems. "Dry Bulk Material Handling Systems: Dense Phase Conveying." 25 June 2003 capture of *
ThomasNet.com. "Types of Heat Exchangers." 11 January 2010 capture of using Internet Archive Wayback Machine *
Xiong, Yiyan. Human-assisted machine translation of Chinese Patent Application Publication number 1861815-A. Published 15 November 2006. Retrieved 25 September 2013. *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Similar Documents

Publication Publication Date Title
US20130037416A1 (en) Method for producing mercury-free alkaline-manganese type electrolyzed manganese dioxide
CN101838736B (zh) 湿法炼锌系统净液钴渣中有价金属的湿法分离方法
CN101845562B (zh) 改进型两矿法生产电解金属锰的装置及方法
CN102912138B (zh) 一种从锌电积阳极泥中回收锌、锰、铅和银的方法
JP2013538936A5 (enExample)
CN111471864A (zh) 一种废旧锂离子电池浸出液中回收铜、铝、铁的方法
CN103572313A (zh) 无汞碱锰型电解二氧化锰的生产方法
CN102094119A (zh) 一种低品位软锰矿湿法浸出制备电解金属锰的方法
CN102220490A (zh) 电解二氧化锰的生产方法
CN104131177B (zh) 一种从电镀锡泥中回收镀锡用精锡的方法
CN103695636A (zh) 一种制备电解二氧化锰的方法
CN103014779B (zh) 一种多级矿浆分解电积槽及分解电积联合工艺
CN103710541B (zh) 湿法生产电解二氧化锰的方法
CN100590230C (zh) 在氯盐介质中金属铅和二氧化锰同时电解的方法
CN106282569A (zh) 一种铜镉渣提镉残渣资源回收的方法
CN106757149A (zh) 一种从电解锌阳极泥中回收锰、铅、银的方法
CN106542506A (zh) 一种从沉碲废液中回收硒的方法
CN109485023A (zh) 一种从含铜碲废液中回收碲的方法
CN107619925A (zh) 一种高效富集硫化锌精矿中铜、铟的工艺
CN104532295A (zh) 电解锌浸出渣中有价金属的回收工艺及其用到的电解槽
CN101871045A (zh) 利用硫酸法钛白废酸生产锌的方法
CN108300855A (zh) 一种含锌氧化物双流程联合浸出并混液电解锌的工艺方法
CN105624727A (zh) 同一电解槽中同时生产电解金属锰和电解二氧化锰的方法
CN104313320B (zh) 一种锌电解液中锌镁的强酸饱和结晶分离方法
CN117210877A (zh) 一种降低阴极铜中银含量的方法及所制得的电解铜材

Legal Events

Date Code Title Description
AS Assignment

Owner name: GUANGXI NON-FERROUS METALS GROUP HUIYUANMENGYE CO.

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CHEN, QIZHI;REEL/FRAME:029043/0947

Effective date: 20120927

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION