CN1059241C - Process for efficiently extracting cobalt compound from leftover containing cobalt - Google Patents

Process for efficiently extracting cobalt compound from leftover containing cobalt Download PDF

Info

Publication number
CN1059241C
CN1059241C CN98111506A CN98111506A CN1059241C CN 1059241 C CN1059241 C CN 1059241C CN 98111506 A CN98111506 A CN 98111506A CN 98111506 A CN98111506 A CN 98111506A CN 1059241 C CN1059241 C CN 1059241C
Authority
CN
China
Prior art keywords
cobalt
acid
solution
heat sink
ammonia
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.)
Expired - Fee Related
Application number
CN98111506A
Other languages
Chinese (zh)
Other versions
CN1249354A (en
Inventor
孔令树
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CN98111506A priority Critical patent/CN1059241C/en
Publication of CN1249354A publication Critical patent/CN1249354A/en
Application granted granted Critical
Publication of CN1059241C publication Critical patent/CN1059241C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

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

  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

The present invention provides new technology for extracting cobalt compounds from leftover material containing cobalt with high efficiency, which comprises the key steps that the acidic solution of the leftover material containing cobalt is ammonified by excessive ammonia water, a solution of cobalt-ammine complexes is separated, and cobalt oxide is separated by adding alkali through heat sink. The method used for extracting the cobalt compounds has high extraction rate and high purity of extracted cobalt oxide.

Description

Novel process for efficiently extracting cobalt oxide from leftovers containing cobalt
The present invention relates to a preparation process of chemical raw material, i.e. a new process for extracting cobalt oxide from cobalt-containing leftovers.
Cobalt is a rare element in nature, and cobalt resources are relatively scarce in the world; with the continuous development of industrial technology, the usage of cobalt compounds is more and more extensive, and the demand is increasingly higher. Due to the lack of resources, the recycling of cobalt element in the waste metal containing cobalt becomes important work for the leftovers containing cobalt generated in industrial production. The currentstate of the art for cobalt recovery is: the leftover containing cobalt produced in industrial production is often mixed with elements such as iron, manganese and the like in cobalt-containing waste metal, and cobalt in the leftover is required to be separated from the iron and the manganese to prepare a high-purity cobalt compound, so that the cobalt is extracted to prepare a useful cobalt compound, for example: cobalt acetate, cobalt oxide, cobalt chloride, basic cobalt carbonate, and the like. The extraction method of most manufacturers at present is to dissolve the waste cobalt-containing metal and cobalt waste metal into mixed salt solution by using sulfuric acid, hydrochloric acid and nitric acid, then adjust the pH value of the solution, oxidize metal ions such as iron and manganese into high-valence iron and manganese hydroxides or oxides by using strong oxidants such as hydrogen peroxide and sodium chlorate, and remove the formed precipitate. This approach has two disadvantages: firstly, the extraction rate is low: the cobalt is partially oxidized into higher oxides or hydroxides during oxidation and is removed together with the precipitate. Secondly, the purity is low: the residual soluble ions of ferromanganese are more, so the purity of the proposed cobalt is low, the field for preparing high-purity cobalt compounds is still unavailable, and the high-purity cobalt compounds can be prepared only by using high-purity cobalt metal at present.
The invention aims to efficiently extract high-purity cobalt oxide from leftovers containing cobalt so as to prepare a high-purity cobalt compound.
In order to achieve the purpose, the process steps and related chemical reaction formulas of the technical scheme are as follows:
1. acid dissolution:
the pH value of the acid solution formed by pretreatment or direct dissolutionin sulfuric acid or hydrochloric acid is kept between 2 and 3 according to the properties of the leftovers
Co is CoSO4CoCl2In solution
Mn is MnSO4MnCl2In solution
Fe is FeSO4FeCl2In solution
Fe2(SO4)3FeCl3In solution
Separating the insoluble substances with separation equipment (centrifuge, filter, etc.) to obtain clear solution.
2. Ammoniation separation:
adding acid-soluble clear mixed acid solution into ammonia water, and maintaining pH at 8-9. The following reactions occur:
co is complexed into cobalt-ammonia complex ions under the action of excessive ammonia and is dissolved in water
Under the action of oxygen in the air, Co (NH)3)4 ++Is oxidized to more stable Co (NH)3)6 +++The complex ions are also soluble in water.
In this case, Fe (OH)2And most of Mn (OH)2Is a precipitate.
The suspension was separated, and the resulting liquid contained a small amount of Mn (OH)2Dissolved in an excess of aqueous ammonia.
Adding Na into the solution2CO3Or NH4HCO3The solution gave the following reaction:
mixing MnCO3The precipitate was separated off. Because of Mn (OH)2Mn (OH) which oxidizes in ammonia solution to produce a brown color when exposed to air4The precipitate is also removed. Only the Co compound remains in solution, separating the cobalt from the ferromanganese.
3. Adding alkali and heat sink:
NaOH is added to the solution and heated to boiling, the following reaction takes place
This resulted in the formation of a cobalt oxide precipitate, ammonia gas evolution, and the liquid was NaCl solution.
4. Absorption:
the ammonia sent from the heating precipitation is absorbed by water and cooled to prepare 120TT (namely 6N) ammonia water for ammoniation.
5. Separation:
the hot precipitate is sent to the suspension where the cobalt oxide is separated from the NaCl solution using a separation device.
6. Washing:
washing the separated cobalt oxide with high-purity water, and further separating to obtain the cobalt oxide with high purity for preparing various cobalt compounds.
The method has the advantages that: 1. the extraction rate is high: due to Co (NH)3)6Cl3Is highly soluble and complex ion stable, and therefore Co (OH)2The precipitate is basically dissolved, so that the invention has high extraction rate, and the experiment proves that the extraction rate can reach more than 95%. 2. The purity is high: at NH3In the presence of Mn (OH)2-MnCO3Very easy to carry out, Fe (OH)3、Fe(OH)2、MnCO3The solubility product is very small, and the manganese ions and the iron ions in the solution are very tiny. Therefore, the high purity of the cobalt sesquioxide is ensured, and pilot scale experiments prove that the Co content in the basic cobalt carbonate prepared by the cobalt oxide reaches 46.9 percent; prepared cobalt acetate Co (CH)3COO)24H2The cobalt acetate content of O reaches 99 percent, which is comparable with the product prepared by high-purity metal cobalt. 3. The conventional preparation of other cobalt compounds from cobalt oxides is easy to carry out.
An embodiment of the invention is described below with reference to the accompanying drawings:
FIG. 1 is a schematic process flow diagram of the present invention.
The method provided by the invention is adopted by the inventor to perform a pilot test in a certain fine chemical plant of Jiangpu, and the specific method is as follows:
1. the raw material is cobalt manganese material recovered by sodium carbonate from waste liquid of terephthalic acid generated by chemical plants of Yangzi group company. The main component of the material is CoCO3、MnCO3The Co content is 10%.
2. The auxiliary raw materials are all market products, and the ammonia water is industrial ammonia water.
3. The description of the examples is carried out according to the inventive procedure.
(1) Acid dissolution: dissolving cobalt and manganese materials in a reaction kettle by using industrial sulfuric acid, and removing residues insoluble in dilute acid organic acid to obtain clear CoSO4、MnSO4The solution was mixed.
(2) Ammoniation: adding industrial ammonia water into an ammoniation device according to the requirements of the invention, slowly adding acid solution, and keeping the pH value above 8-9.
(3) Separation: separating out the precipitate by using a 800 centrifugal machine, adding a sodium carbonate solution into the liquid for precipitation and clarification, and then sending the liquid into a reaction kettle.
(4) Adding alkali and heat sink: NaOH was added to the kettle and heated to boiling temperature of 100 ℃ for 5 minutes.
(5) Separation and washing: the suspension of the heat sink was cooled to 60 degrees and sent to a 800 centrifuge to separate the cobalt oxide and the filter cake was washed five times with high purity water.
(6) Dissolving: the filter cake cobalt oxide was dissolved and diluted with concentrated sulfuric acid in a reaction kettle.
(7) Separation: separating the dissolved cobalt sulfate solution by a centrifugal machine to obtain a clear solution, wherein the filter cake is undissolved Co2O3And putting the mixture into a kettle for redissolving.
(8) And (3) precipitation: feeding the cobalt sulfate solution into a precipitation tank (3 cubic meters of stainless steel stirring tank) and adding Na2CO3The solution was brought to pH 8 and a purple-red precipitate formed.
(9) Separation: the suspension containing the purplish red precipitate was sent to 800 centrifuges, Na was added2SO4The solution is separated outThe purple filter cake is washed with high-purity water for three times.
(10) Washing: and (4) sending the filter cake into a washing tank, adding high-purity water, stirring and washing.
(11) Separating the washed suspension in 800-type centrifuge, washing with high-purity water for several times, and adding BaCl into the filtrate2The solution did not precipitate white.
(12) Drying and crushing: and drying the filter cake in a tray and crushing the filter cake into a green bean large-grain basic cobalt carbonate product.
(13) The product has a cobalt content of 46.40% as analyzed by a chemical university analysis and research laboratory.

Claims (6)

1. The process of extracting cobalt oxide from leftover with cobalt includes the following steps:
(1) acid dissolution;
(2) ammoniation separation;
(3) adding alkali to the heat sink;
(4) absorption;
(5) separating and washing.
2. The method of claim 1 wherein the cobalt-containing leftovers comprise cobalt-containing waste metals of the elements cobalt, iron and manganese.
3. The method of claim 1 or 2, wherein the acid dissolution treatment of the cobalt-containing tailings is carried out by pre-treating the tailings or directly dissolving the tailings in sulfuric acid or hydrochloric acid, and the pH value of the acid solution is maintained at 2-3.
4. The process according to any of the preceding claims, wherein the ammoniated separation is carried out by adding an excess of aqueous ammonia to the acid-soluble clear mixed acid solution, maintaining the pH at 8-9.
5. A method according to any one of the preceding claims wherein the alkalising heat sink is heated to boiling by adding caustic soda to a solution based on cobalt ammine complexes.
6. A process according to any one of the preceding claims wherein the ammonia gas evolved in the step of adding an alkaline heat sink is cooled by water absorption to make 6 equivalents of ammonia for ammoniation.
CN98111506A 1998-09-25 1998-09-25 Process for efficiently extracting cobalt compound from leftover containing cobalt Expired - Fee Related CN1059241C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN98111506A CN1059241C (en) 1998-09-25 1998-09-25 Process for efficiently extracting cobalt compound from leftover containing cobalt

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN98111506A CN1059241C (en) 1998-09-25 1998-09-25 Process for efficiently extracting cobalt compound from leftover containing cobalt

Publications (2)

Publication Number Publication Date
CN1249354A CN1249354A (en) 2000-04-05
CN1059241C true CN1059241C (en) 2000-12-06

Family

ID=5221479

Family Applications (1)

Application Number Title Priority Date Filing Date
CN98111506A Expired - Fee Related CN1059241C (en) 1998-09-25 1998-09-25 Process for efficiently extracting cobalt compound from leftover containing cobalt

Country Status (1)

Country Link
CN (1) CN1059241C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100381364C (en) * 2004-08-09 2008-04-16 孔令树 Tervalence cobalt compounds production and lithium cobalt oxide production method using same
CN105274345A (en) * 2015-11-27 2016-01-27 江苏理工学院 Method for separating and recovering cobalt and manganese in cobalt-manganese waste

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100758403B1 (en) * 2004-06-11 2007-09-14 도시바 캐리어 가부시키 가이샤 Hermetic rotary compressor
CN105463215B (en) * 2015-11-27 2018-02-06 江苏理工学院 Method for preparing cobalt product from cobalt-ammonia complex
CN106517245B (en) * 2016-11-23 2019-02-19 荆门市格林美新材料有限公司 A kind of method that ammonium chloride solution removes cobalt

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100381364C (en) * 2004-08-09 2008-04-16 孔令树 Tervalence cobalt compounds production and lithium cobalt oxide production method using same
CN105274345A (en) * 2015-11-27 2016-01-27 江苏理工学院 Method for separating and recovering cobalt and manganese in cobalt-manganese waste
CN105274345B (en) * 2015-11-27 2017-09-29 江苏理工学院 Method for separating and recovering cobalt and manganese in cobalt-manganese waste
CN107828965A (en) * 2015-11-27 2018-03-23 江苏理工学院 Method for separating and recovering cobalt and manganese in cobalt-manganese waste
CN107828965B (en) * 2015-11-27 2019-04-23 江苏理工学院 Method for separating and recovering cobalt and manganese in cobalt-manganese waste

Also Published As

Publication number Publication date
CN1249354A (en) 2000-04-05

Similar Documents

Publication Publication Date Title
KR102008582B1 (en) A Method for Preparing Nickel-Cobalt-Manganese Complex Sulfate Solution by Recycling A Waste Cathode Material of Lithium Secondary Battery Using Solvent Extraction Process to Control Impurities
CN102206755B (en) Method for separating and recovering valuable elements from neodymium-iron-boron wastes
KR101823952B1 (en) A Method For Preparing Lithium Carbonate By Recycling Lithium From Used Anode Of Lithium Ion Seondary Battery
CN102602974B (en) Method for producing less-barium fine strontium salts from celestite
CN112375910B (en) Recovery processing method of waste power battery powder
WO2022213678A1 (en) Method for recycling aluminum in waste positive electrode sheet by using selective leaching and application thereof
CN112320780B (en) Method for recycling iron phosphate waste
KR20170061206A (en) Collection method of precursor material using disposed lithum-ion battery
CN110669933A (en) Method for removing fluorine in nickel-cobalt-manganese solution
CN103466683B (en) A kind of preparation method of high-purity electroplating-gradecopper copper oxide
CN113122725A (en) Method for improving metal recovery rate and purity of waste lithium battery
KR101997983B1 (en) A Preparing Method Of Nickel-Cobalt-Manganese Complex Sulphate Solution Having Low Concentration Of Calcium Ion By Recycling A Wasted Lithium Secondary Battery Cathode Material
CN111180819B (en) Preparation method of battery-grade Ni-Co-Mn mixed solution and battery-grade Mn solution
CN1059241C (en) Process for efficiently extracting cobalt compound from leftover containing cobalt
CN111137869A (en) Preparation method of lithium iron phosphate
CN102897804A (en) Method for preparing lithium carbonate directly from lithium chloride and carbon dioxide
CA1303360C (en) Hydrometallurgical process for the production of beryllium
WO2023005031A1 (en) Preparation method for nickel-cobalt-manganese ternary precursor material and lithium ion battery
CN113354048B (en) Heavy metal precipitator, application and preparation method thereof, and waste acid wastewater treatment method
CN116675197A (en) Method for preparing ferric phosphate from iron phosphate slag after lithium extraction from waste lithium iron phosphate anode powder
CN1631797A (en) Method for extracting vanadium pentoxide from vanadium-containing spent catalyst and petroleum ash
KR20230136948A (en) Selective recovery method of valuable metals using solvent extraction from lithium secondary battery waste
CN114560767A (en) Method for preparing ferrous oxalate by siderite
CN105349789B (en) Method for separating and recovering cobalt and manganese in low-cobalt high-manganese waste by using ammonia-sodium carbonate
CN115109931B (en) Method for recycling multiple metals from tungsten-molybdenum waste residues

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
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee