CN1800422A - Method for processing cobalt copper alloy - Google Patents

Method for processing cobalt copper alloy Download PDF

Info

Publication number
CN1800422A
CN1800422A CNA2005100620166A CN200510062016A CN1800422A CN 1800422 A CN1800422 A CN 1800422A CN A2005100620166 A CNA2005100620166 A CN A2005100620166A CN 200510062016 A CN200510062016 A CN 200510062016A CN 1800422 A CN1800422 A CN 1800422A
Authority
CN
China
Prior art keywords
cobalt
copper alloy
copper
slip
handling
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.)
Granted
Application number
CNA2005100620166A
Other languages
Chinese (zh)
Other versions
CN1333089C (en
Inventor
陈刚
冯德茂
应明明
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.)
YINGLIAN SCIENCE-TECHNOLOGY Co Ltd ZHEJIANG
Original Assignee
YINGLIAN SCIENCE-TECHNOLOGY Co Ltd ZHEJIANG
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 YINGLIAN SCIENCE-TECHNOLOGY Co Ltd ZHEJIANG filed Critical YINGLIAN SCIENCE-TECHNOLOGY Co Ltd ZHEJIANG
Priority to CNB2005100620166A priority Critical patent/CN1333089C/en
Publication of CN1800422A publication Critical patent/CN1800422A/en
Application granted granted Critical
Publication of CN1333089C publication Critical patent/CN1333089C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Abstract

The invention discloses a method for processing the cobalt copper alloy, which comprises the following steps: 1) machine activating program: sending the cobalt copper alloy to the ball crusher to do cruse milling, sending it to the pipe crusher to do correct grinding, then the cobalt copper alloy powder has high internal energy, surface energy and rate surface area so that it has high reacting activity; 2) extracting process: adding the cobalt copper alloy powder in the reacting extraction groove and adding water and muriatic acid by a certain ratio to heat stir on catalyzed oxidation condition so that the cobalt and copper mental 90%-99% extracting of the cobalt copper alloy enters into the solution; 3) Magnetic separating program: separating the residual cobalt copper alloy of the extracting slip and the slip by the magnetic separator, dosing filter solid-liquid separation to the magnetic separated slip to obtain the solution with cobalt and copper.

Description

A kind of method of handling cobalt-copper alloy
Technical field
The present invention relates to a kind of method of handling cobalt-copper alloy, particularly a kind of method with the wet processing cobalt-copper alloy.
Background technology
Cobalt-copper alloy is the important source material of producing cobalt metal and various cobalt products, is commonly called as cobalt white metal or cobalt red alloy or cobalt AB alloy, mainly originates from Africa.Cobalt-copper alloy makes by electric furnace reduction melting cupric oxide cobalt concentrate and the copper slag that contains cobalt, generally contains cobalt: 10%-40%, copper: 10%-50%, iron: 5%-50%, nickel: 0.1%-5%, manganese: 0.1%-5%.This alloy raw material intractability is bigger, and subject matter is that the yield of cobalt, copper is low, cost is high, technical process is long.
The method of handling cobalt-copper alloy at present mainly contains:
1, electro-dissolving: in electrolyzer, be anode, in sulfuric acid or hydrochloric acid system, make cobalt, copper enter solution from the anode dissolving by electrolysis with the cobalt-copper alloy raw material, manganese, iron, nickel also together dissolving enter solution.This method current efficiency is lower, power consumption is higher, and the rate of recovery of cobalt is lower.
2, sulfuration lixiviation process: the cobalt-copper alloy raw material is added sulphur or sulfide (as sulfurous iron ore) sulfuration under 1300 ℃ of-1400 ℃ of temperature, after the oxidation blowing deironing, obtain Co-Cu ice sulfonium and leach the solution that obtains containing cobalt, copper through high pressure.This method production capacity is big, technical process is long, energy consumption is high, and the total recovery of cobalt, copper is lower.
3, High Temperature High Pressure lixiviation process: leach by one section normal pressure and one section High Temperature High Pressure leaching with sulfuric acid or hydrochloric acid, make cobalt, copper leaching in the cobalt-copper alloy enter solution.This method technical process is long, equipment is complicated, must solve the anticorrosion problem of equipment under high temperature, the condition of high voltage.
4, chlorine lixiviation process: this method is to carry out in airtight reactor, behind cobalt-copper alloy and hydrochloric acid adding reactor, feeds chlorine and carries out oxidation dissolution.The leaching yield of this method cobalt, copper, iron higher (mining and metallurgy, 1997, Vol6 (1): 67-69), but equipment complexity, equipment anticorrosion and environmental requirement height.
5, direct pickling process: leach with sulfuric acid, hydrochloric acid or nitric acid or two kinds of composition mixing acid wherein.This method is under normal pressure, and speed of response is slow, and leaching process efficient is not high, and technical process is long, the production cost height.
In addition, above-mentioned the whole bag of tricks enters leach liquor because a large amount of iron also leaches simultaneously, and the iron removal of postorder will cause the loss of cobalt, copper, directly influence the rate of recovery of cobalt, copper.
Summary of the invention
For overcoming existing treatment process above shortcomings, the invention provides that a kind of technical process is short, production cost is low, cobalt copper leaching rate and the high a kind of method of handling cobalt-copper alloy of casting yield.The technical solution adopted for the present invention to solve the technical problems is that it may further comprise the steps:
(1), mechanical activation operation: at first cobalt-copper alloy is sent into ball mill or Raymond mill is roughly ground, and then send into tuber grinder or vibrations mill or mechanical stirring mill and carry out fine grinding, by making the cobalt-copper alloy powder have high interior energy, surface energy and high specific surface area behind two sections mills, and then make the cobalt-copper alloy powder have high reactive behavior;
(2), leach operation: will add reactive tank through the cobalt-copper alloy powder or the slip of mechanical activation, add entry, hydrochloric acid, catalyzer, oxygenant with schedule of operation according to a certain percentage, under heating, agitation condition, make cobalt, copper valuable metal 90%-99% leaching in the cobalt-copper alloy enter solution;
(3), magnetic separation separation circuit: utilize the cobalt-copper alloy magnetic properties different with leached mud, to leach by the low intensity magnetic separation machine that unreacted small portion of residual cobalt-copper alloy separates with slip in the slip, slip after the magnetic separation filters by B, makes solid-liquid separation, can obtain being rich in the solution of cobalt, copper.
The median size of the cobalt-copper alloy powder of process mechanical activation is between 10 μ m-150 μ m.
Liquid-solid ratio in the reactive tank is 3: 1-12: 1.
The add-on of hydrochloric acid is the 75%-150% of theoretical amount, and the pH value of reaction end is controlled between the 2.0-4.5.
The temperature of reaction that leaches operation is controlled between 65 ℃-95 ℃, and the reaction times is controlled between the 200min-900min.
Described catalyzer is to contain at least a in the inorganic salt of halogens, described inorganic salt are Repone K, sodium-chlor, iron(ic) chloride, iron protochloride, cupric chloride, ammonium chloride, sodium chlorate, Sodium Fluoride, Neutral ammonium fluoride, ammonium bifluoride, and catalyst concn control is not more than 150g/L.。
Described oxygenant is at least a in air, the oxygen, and its flow control is at every cubic metre of slip 0.2-2.0 cubic meter.
The small portion of residual cobalt-copper alloy that magneticly elects turns back to the mechanical activation operation or leaches operation.
After adopting aforesaid method, following characteristics are arranged: the one, technical process is short, under condition of normal pressure, can make the leaching yield of cobalt in the cobalt-copper alloy, copper reach 90%-99%, and the iron rule in the alloy is stayed in the leached mud with the form of ferric oxide or pyrrhosiderite; The 2nd, simple to operate, be easy to control; The 3rd, it is very fast to leach speed of response, and it is higher to leach operating efficiency; The 4th, the leaching yield height of cobalt and copper, the casting yield height of cobalt and copper; Five reduced investments, production cost is lower.
Embodiment
Below in conjunction with specific embodiments main processes of the present invention is sketched: it may further comprise the steps:
(1), mechanical activation operation: at first cobalt-copper alloy is sent into ball mill or Raymond mill is roughly ground, and then send into tuber grinder or vibrations mill or mechanical stirring mill and carry out fine grinding, by making the cobalt-copper alloy powder have high interior energy, surface energy and high specific surface area behind two sections mills, and then make the cobalt-copper alloy powder have high reactive behavior; The median size of the cobalt-copper alloy powder of process mechanical activation is between 10 μ m-150 μ m.
(2), leach operation: at first will add reactive tank through the cobalt-copper alloy powder or the slip of mechanical activation, then by the liquid-solid ratio 3 in the reactive tank: 1-12: 1 adds entry; 75%-150% by theoretical amount adds hydrochloric acid; Add catalyzer by the amount that is not more than 150g/L, catalyzer is contain the halogen element inorganic salt a kind of at least, also can be several combinations, described inorganic salt can be Repone K, sodium-chlor, iron(ic) chloride, iron protochloride, cupric chloride, ammonium chloride, sodium chlorate, Sodium Fluoride, Neutral ammonium fluoride, ammonium bifluoride; Stir then, the rotating speed of stirring rake is 80-350 rev/min; Be blown into air or oxygen, flow control is at every cubic metre of slip 0.2-2.0 cubic meter; With steam or electricity slip is heated between 65 ℃-95 ℃; Reaction times is controlled between the 300min-900min; By the relative quantity or the adding neutralizing agent of control reactive tank internal reaction material, the pH value of control reaction end, the pH value is controlled between the 2.0-4.5, makes cobalt, copper valuable metal 90%-99% leaching in the cobalt-copper alloy enter solution.
On the catalyzed oxidation leaching process, cobalt-copper alloy and hydrochloric acid can also can add in batches in disposable adding; The degree of the add-on of catalyzer and the mechanical activation of cobalt-copper alloy is relevant with the ionic strength of leach liquor; When the degree of mechanical activation is good, can add less or not add, excessive catalyzer can cause the passivation of alloy; The amount of blasting of oxygenant air or oxygen can be different in initial stage, mid-term and the later stage of reaction, oxygenant should be in reactive tank homodisperse, guarantee and fully the contacting of feed liquid.
(3), magnetic separation separation circuit: magnetic separation is the important means of simplifying leaching operation, quickening leaching velocity and guaranteeing cobalt, copper casting yield; Cobalt-copper alloy has stronger ferromegnetism, and leached mud does not have, and utilizes cobalt-copper alloy different with the magnetic properties of leached mud, will leach by the low intensity magnetic separation machine that unreacted small portion of residual cobalt-copper alloy separates with slip in the slip; The cobalt-copper alloy that magneticly elects is back to the mechanical activation operation or leaches operation; Filter by B through the slip after the magnetic separation, make solid-liquid separation, can obtain being rich in the solution of cobalt, copper.A series of problems that the chemical equilibrium of reactive tank internal reaction material causes have been solved well by magnetic separation.Because, the one, the cobalt-copper alloy powder in the reactive tank and hydrochloric acid add-on are difficult to accomplish just in time to add by the dosage of equivalent chemical reaction, even accomplish or near equivalent, speed is also very slow when reacting near terminal point; The 2nd, for fast reaction speed, one of them that must make cobalt-copper alloy or hydrochloric acid in the reaction leaching vat is excessive; The 3rd, in order to guarantee the leaching yield of cobalt, copper, must add excessive hydrochloric acid, and excessive hydrochloric acid will increase difficulty to the control of reaction process pH value, the consumption of material also will increase.
Enter leach liquor in order to prevent that a large amount of iron from also leaching simultaneously, add-on that can be by catalyzer, oxygenant and hydrochloric acid and temperature of reaction and reaction times are controlled the leaching of iron in the cobalt-copper alloy; After adopting aforesaid method, the leaching yield of iron is less than 1.0%, and the content of iron can be controlled in below the 0.5g/L in the leach liquor, the minimum 5PPm that reaches.
Be that the cobalt-copper alloy of cobalt 28.7%, copper 26.3%, iron 23.5%, nickel 1.08%, manganese 0.89% is illustrated with major ingredient below.
Embodiment one gets cobalt-copper alloy 1000 grams and put into the ball mill mill 90 minutes, and then shakes mill 120 minutes, and median size is 47 microns.Weigh this alloy 80 grams, ammonium chloride 80 grams, iron(ic) chloride 20 grams, 133 milliliters of 36% hydrochloric acid add 500 milliliters in water, heat up to be heated to 87 degree, bubbling air (flow is 1.2 liters/minute), reaction is 8 hours under agitation condition, and reaction end pH value is 3.5.Then slip is carried out magnetic separation, filtration.Magneticly elect unreacted remaining cobalt-copper alloy 2.6 grams, the leach liquor that obtains contains cobalt 26.9 grams per liters, copper 24.8 grams per liters, iron 0.06 grams per liter.Leached mud contains cobalt 0.42 gram, copper 0.30 gram.The leaching yield of cobalt is 94.3%, and the leaching yield of copper is 95.2%.The casting yield of cobalt is 98.0%, and the casting yield of copper is 98.3%.
Embodiment two gets cobalt-copper alloy 1000 grams and put into the ball mill mill 90 minutes, and then shakes mill 120 minutes, and median size is 47 microns.Weigh this alloy 80 grams, ammonium chloride 50 grams, Sodium Fluoride 30 grams, 133 milliliters of 36% hydrochloric acid add 500 milliliters in water, heat up to be heated to 87 degree, bubbling air (flow is 1.2 liters/minute), reaction is 8 hours under agitation condition, and reaction end p H value is 3.5.Then slip is carried out magnetic separation, filtration.Magneticly elect unreacted remaining cobalt-copper alloy 2.1 grams, the leach liquor that obtains contains cobalt 32.8 grams per liters, copper 27.6 grams per liters, iron 0.08 grams per liter.Leached mud contains cobalt 0.31 gram, copper 0.33 gram.The leaching yield of cobalt is 95.8%, and the leaching yield of copper is 95.5%.The casting yield of cobalt is 98.4%, and the casting yield of copper is 98.2%.
Embodiment three gets cobalt-copper alloy 1000 grams and put into the ball mill mill 90 minutes, and then shakes mill 120 minutes, and median size is 47 microns.Weigh this alloy 160 grams, ammonium chloride 50 grams, Sodium Fluoride 30 grams, iron(ic) chloride 20 grams, 266 milliliters of 36% hydrochloric acid, add 500 milliliters in water, intensification is heated to 87 degree, bubbling air (flow is 1.5 liters/minute), and reaction is after 6.5 hours under agitation condition, slowly sodium hydroxide solution to the pH value of adding 5% is 4.0, continues reaction 45 minutes.Then slip is carried out magnetic separation, filtration.Magneticly elect unreacted remaining cobalt-copper alloy 3.5 grams, the leach liquor that obtains contains cobalt 57.2 grams per liters, copper 50.0 grams per liters, iron 0.005 grams per liter.Leached mud contains cobalt 0.39 gram, copper 0.77 gram.The leaching yield of cobalt is 96.6%, and the leaching yield of copper is 95.6%.The casting yield of cobalt is 98.9%, and the casting yield of copper is 97.3%.
Embodiment four cobalt-copper alloys 1000 grams were put into the ball mill mill 90 minutes, and then shook mill 120 minutes, and median size is 47 microns.Weigh these alloy 135 grams and magneticly elect and leach unreacted cobalt-copper alloy 25 grams in the slip, ammonium chloride 50 grams, Sodium Fluoride 30 grams, iron(ic) chloride 20 grams, 266 milliliters of 36% hydrochloric acid, add 500 milliliters in water, intensification is heated to 87 degree, bubbling air (flow is 1.5 liters/minute), and reaction is 6.5 hours under agitation condition, slowly adding ammonia to pH value is 4.0, continues reaction 45 minutes.Then slip is carried out magnetic separation, filtration.Magneticly elect unreacted remaining cobalt-copper alloy 4.2 grams, the leach liquor that obtains contains cobalt 54.2 grams per liters, copper 51.3 grams per liters, iron 0.006 grams per liter.Leached mud contains cobalt 0.15 gram, copper 0.83 gram.The leaching yield of cobalt is 96.7%, and the leaching yield of copper is 94.4%.The casting yield of cobalt is 99.2%, and the casting yield of copper is 97.5%.

Claims (8)

1, a kind of method of handling cobalt-copper alloy, it is characterized in that: it may further comprise the steps:
(1), mechanical activation operation: at first cobalt-copper alloy is sent into ball mill or Raymond mill is roughly ground, and then send into tuber grinder or vibrations mill or mechanical stirring mill and carry out fine grinding, by making the cobalt-copper alloy powder have high interior energy and surface energy and high specific surface area behind two sections mills, and then make the cobalt-copper alloy powder have high reactive behavior;
(2), leach operation: will add reactive tank through the cobalt-copper alloy powder or the slip of mechanical activation, add entry, hydrochloric acid, catalyzer, oxygenant with schedule of operation according to a certain percentage, under heating, agitation condition, make cobalt, copper valuable metal 90%-99% leaching in the cobalt-copper alloy enter solution;
(3), magnetic separation separation circuit: utilize the cobalt-copper alloy magnetic properties different with leached mud, to leach by the low intensity magnetic separation machine that unreacted small portion of residual cobalt-copper alloy separates with slip in the slip, slip after the magnetic separation filters by B, makes solid-liquid separation, can obtain being rich in the solution of cobalt, copper.
2, a kind of method of handling cobalt-copper alloy according to claim 1 is characterized in that: the median size of the cobalt-copper alloy powder of process mechanical activation is between 10 μ m-150 μ m.
3, a kind of method of handling cobalt-copper alloy according to claim 1 is characterized in that: the liquid-solid ratio in the reactive tank is 3: 1-12: 1.
4, a kind of method of handling cobalt-copper alloy according to claim 1, it is characterized in that: the add-on of hydrochloric acid is the 75%-150% of theoretical amount, the pH value of reaction end is controlled between the 2.0-4.5.
5, a kind of method of handling cobalt-copper alloy according to claim 1 is characterized in that: the temperature of reaction that leaches operation is controlled between 65 ℃-95 ℃, and the reaction times is controlled between the 200min-900min.
6, a kind of method of handling cobalt-copper alloy according to claim 1, it is characterized in that: described catalyzer is to contain at least a in the inorganic salt of halogens, described inorganic salt are Repone K, sodium-chlor, iron(ic) chloride, iron protochloride, cupric chloride, ammonium chloride, sodium chlorate, Sodium Fluoride, Neutral ammonium fluoride, ammonium bifluoride, and catalyst concn control is not more than 150g/L.
7, a kind of method of handling cobalt-copper alloy according to claim 1 is characterized in that: described oxygenant is at least a in air, the oxygen, and its flow control is at every cubic metre of slip 0.2-2.0 cubic meter.
8, a kind of method of handling cobalt-copper alloy according to claim 1 is characterized in that: the small portion of residual cobalt-copper alloy that magneticly elects turns back to the mechanical activation operation or leaches operation.
CNB2005100620166A 2005-12-13 2005-12-13 Method for processing cobalt copper alloy Expired - Fee Related CN1333089C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100620166A CN1333089C (en) 2005-12-13 2005-12-13 Method for processing cobalt copper alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100620166A CN1333089C (en) 2005-12-13 2005-12-13 Method for processing cobalt copper alloy

Publications (2)

Publication Number Publication Date
CN1800422A true CN1800422A (en) 2006-07-12
CN1333089C CN1333089C (en) 2007-08-22

Family

ID=36810630

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100620166A Expired - Fee Related CN1333089C (en) 2005-12-13 2005-12-13 Method for processing cobalt copper alloy

Country Status (1)

Country Link
CN (1) CN1333089C (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100345986C (en) * 2006-08-04 2007-10-31 湖南瑞翔新材料有限公司 Method for extracting valence metal from copper ferrocobalt alloy
CN101818246A (en) * 2010-05-11 2010-09-01 南通新玮镍钴科技发展有限公司 Technology for leaching cobalt-copper white alloy
CN101157982B (en) * 2006-10-08 2011-04-06 中国恩菲工程技术有限公司 Method for leaching bidery metal by sulfuric acid and inflation agitation leaching trough
CN102392126A (en) * 2011-11-17 2012-03-28 森松(江苏)海油工程装备有限公司 Activating acid leaching method for extracting vanadium from bone coal
CN101768669B (en) * 2010-01-28 2012-07-25 浙江华友钴业股份有限公司 Method for processing cobalt-copper alloy at room temperature
CN103128288A (en) * 2011-11-22 2013-06-05 元磁新型材料(苏州)有限公司 Metal crystal powder and production method and production device thereof
CN105755283A (en) * 2016-03-08 2016-07-13 江西理工大学 Method for selectively leaching valuable metals in laterite-nickel ore by aid of chloride
CN106040409A (en) * 2016-08-24 2016-10-26 孙召华 Ore-dressing system and ore-dressing technology for reducing content of sulphur in iron ore concentrate and for sorting cobalt concentrate
CN109652651A (en) * 2017-10-10 2019-04-19 中国石油化工股份有限公司 The method of the useless activation of cobalt molybdenum base hydrotreating catalyst Call Provision and molybdenum
CN109897968A (en) * 2019-04-21 2019-06-18 湖南金源新材料股份有限公司 A method of leaching rate is improved using ultra-fine grinding mill processing lithium battery reworked material
CN110629223A (en) * 2019-10-15 2019-12-31 上海第二工业大学 Deplating method for metal coating on surface of waste ABS electroplated part
CN112609090A (en) * 2020-11-19 2021-04-06 中国恩菲工程技术有限公司 Separation method of copper-cobalt oxide ore
US11319613B2 (en) 2020-08-18 2022-05-03 Enviro Metals, LLC Metal refinement

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58740B2 (en) * 1977-12-27 1983-01-07 住友金属鉱山株式会社 Method for separating valuable metals from alloys containing rare earth elements

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100345986C (en) * 2006-08-04 2007-10-31 湖南瑞翔新材料有限公司 Method for extracting valence metal from copper ferrocobalt alloy
CN101157982B (en) * 2006-10-08 2011-04-06 中国恩菲工程技术有限公司 Method for leaching bidery metal by sulfuric acid and inflation agitation leaching trough
CN101768669B (en) * 2010-01-28 2012-07-25 浙江华友钴业股份有限公司 Method for processing cobalt-copper alloy at room temperature
CN101818246A (en) * 2010-05-11 2010-09-01 南通新玮镍钴科技发展有限公司 Technology for leaching cobalt-copper white alloy
CN101818246B (en) * 2010-05-11 2012-05-23 南通新玮镍钴科技发展有限公司 Leaching treatment process of cobalt-copper white alloy
CN102392126A (en) * 2011-11-17 2012-03-28 森松(江苏)海油工程装备有限公司 Activating acid leaching method for extracting vanadium from bone coal
CN103128288A (en) * 2011-11-22 2013-06-05 元磁新型材料(苏州)有限公司 Metal crystal powder and production method and production device thereof
CN105755283A (en) * 2016-03-08 2016-07-13 江西理工大学 Method for selectively leaching valuable metals in laterite-nickel ore by aid of chloride
CN106040409A (en) * 2016-08-24 2016-10-26 孙召华 Ore-dressing system and ore-dressing technology for reducing content of sulphur in iron ore concentrate and for sorting cobalt concentrate
CN109652651A (en) * 2017-10-10 2019-04-19 中国石油化工股份有限公司 The method of the useless activation of cobalt molybdenum base hydrotreating catalyst Call Provision and molybdenum
CN109897968A (en) * 2019-04-21 2019-06-18 湖南金源新材料股份有限公司 A method of leaching rate is improved using ultra-fine grinding mill processing lithium battery reworked material
CN110629223A (en) * 2019-10-15 2019-12-31 上海第二工业大学 Deplating method for metal coating on surface of waste ABS electroplated part
US11319613B2 (en) 2020-08-18 2022-05-03 Enviro Metals, LLC Metal refinement
US11578386B2 (en) 2020-08-18 2023-02-14 Enviro Metals, LLC Metal refinement
CN112609090A (en) * 2020-11-19 2021-04-06 中国恩菲工程技术有限公司 Separation method of copper-cobalt oxide ore

Also Published As

Publication number Publication date
CN1333089C (en) 2007-08-22

Similar Documents

Publication Publication Date Title
CN1800422A (en) Method for processing cobalt copper alloy
US11459636B2 (en) Method and system for comprehensive recovery and utilization of copper-nickel sulfide ore
CA2856341C (en) Method for producing high-purity nickel sulfate
CN102994747B (en) Technology for recovering metallic copper from high-lead copper matte
CA2788384C (en) Process for the recovery of titanium dioxide and value metals by reducing the concentration of hydrochloric acid in leach solution and system for same
CN101818250B (en) Method for processing cobalt-copper-iron alloy
CN106119560B (en) Zinc-cobalt separation method
CN101844750A (en) Method for preparing high-purity tellurium by material containing tellurium
AU2013362874A1 (en) Method for producing a solid scandium-containing material of enhanced scandium content
WO2018101039A1 (en) Ion exchange processing method, and scandium recovery method
CN112458280A (en) Method for extracting valuable metals by leaching low grade nickel matte with acidic etching solution
CN107475519A (en) A kind of method of copper and arsenic in separation copper arsenic slag
CN111411224B (en) Beneficiation method for comprehensively recovering and combining silver and copper from low-grade manganese-containing ore
CN105399132B (en) A kind of technique for preparing basic copper chloride and basic zinc chloride with brass clinker and flue dust containing zinc
CN108441649B (en) Method for extracting nickel from chemical precipitation nickel sulfide material
CN1265003C (en) Method for chloridizing roasting and ammonia extraction of silver and manganese products for manganese silver finished ore
WO2015171010A1 (en) Process of extracting gold and silver from ores and mining by-products
CN110629043B (en) Bismuth extraction method based on phase transformation of bismuth sulfide ore
CN114606388A (en) Method for leaching arsenic-containing copper smelting smoke and synchronously removing arsenic
CN104711431B (en) A kind of method that copper dross slag produces copper sulphate
CN113582252A (en) Preparation method of nickel-cobalt-manganese ternary precursor material and lithium ion battery
FI131084B1 (en) Process for metal sulphidation
WO2023237713A1 (en) Sulphidation of a solid metal feed comprising ni and/or co
CN114990351A (en) Method for co-processing zinc concentrate and copper white smoke
CN117965907A (en) Method for preparing high-purity magnesium salt solution from mineral tailings by normal pressure and oxygen pressure coupling acid leaching

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070822

Termination date: 20121213