CN107739828A - Method for separating and recovering cobalt and manganese in low-cobalt high-manganese waste by using ammonia-ammonium carbonate - Google Patents
Method for separating and recovering cobalt and manganese in low-cobalt high-manganese waste by using ammonia-ammonium carbonate Download PDFInfo
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- CN107739828A CN107739828A CN201710903720.2A CN201710903720A CN107739828A CN 107739828 A CN107739828 A CN 107739828A CN 201710903720 A CN201710903720 A CN 201710903720A CN 107739828 A CN107739828 A CN 107739828A
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- Prior art keywords
- cobalt
- manganese
- ammonia
- solution
- ammonium carbonate
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- 239000010941 cobalt Substances 0.000 title claims abstract description 94
- 229910017052 cobalt Inorganic materials 0.000 title claims abstract description 94
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 title claims abstract description 90
- 239000011572 manganese Substances 0.000 title claims abstract description 78
- 229910052748 manganese Inorganic materials 0.000 title claims abstract description 74
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 title claims abstract description 72
- 239000002699 waste material Substances 0.000 title claims abstract description 44
- 238000000034 method Methods 0.000 title claims abstract description 32
- FWABRVJYGBOLEM-UHFFFAOYSA-N diazanium;azane;carbonate Chemical compound N.[NH4+].[NH4+].[O-]C([O-])=O FWABRVJYGBOLEM-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 239000000243 solution Substances 0.000 claims abstract description 67
- 238000011084 recovery Methods 0.000 claims abstract description 40
- 238000006243 chemical reaction Methods 0.000 claims abstract description 31
- WRWZNPYXEXPBAY-UHFFFAOYSA-N azane cobalt Chemical compound N.[Co] WRWZNPYXEXPBAY-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000011259 mixed solution Substances 0.000 claims abstract description 16
- 239000011656 manganese carbonate Substances 0.000 claims abstract description 11
- 235000006748 manganese carbonate Nutrition 0.000 claims abstract description 11
- 229940093474 manganese carbonate Drugs 0.000 claims abstract description 11
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 claims abstract description 11
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 claims abstract description 11
- 238000001914 filtration Methods 0.000 claims abstract description 9
- 239000002244 precipitate Substances 0.000 claims abstract description 8
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims abstract description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 45
- 239000000463 material Substances 0.000 claims description 35
- 239000002253 acid Substances 0.000 claims description 33
- MZZUATUOLXMCEY-UHFFFAOYSA-N cobalt manganese Chemical compound [Mn].[Co] MZZUATUOLXMCEY-UHFFFAOYSA-N 0.000 claims description 26
- 238000000926 separation method Methods 0.000 claims description 21
- 239000003638 chemical reducing agent Substances 0.000 claims description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 15
- 235000011121 sodium hydroxide Nutrition 0.000 claims description 15
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 11
- 239000001099 ammonium carbonate Substances 0.000 claims description 11
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 11
- 230000029087 digestion Effects 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 8
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 7
- 238000002156 mixing Methods 0.000 claims description 7
- NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 claims description 6
- 229910021503 Cobalt(II) hydroxide Inorganic materials 0.000 claims description 6
- ASKVAEGIVYSGNY-UHFFFAOYSA-L cobalt(ii) hydroxide Chemical compound [OH-].[OH-].[Co+2] ASKVAEGIVYSGNY-UHFFFAOYSA-L 0.000 claims description 6
- IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 229910021529 ammonia Inorganic materials 0.000 claims description 5
- 239000000706 filtrate Substances 0.000 claims description 5
- 239000012279 sodium borohydride Substances 0.000 claims description 5
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 5
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 4
- 229930040373 Paraformaldehyde Natural products 0.000 claims description 4
- MULYSYXKGICWJF-UHFFFAOYSA-L cobalt(2+);oxalate Chemical compound [Co+2].[O-]C(=O)C([O-])=O MULYSYXKGICWJF-UHFFFAOYSA-L 0.000 claims description 4
- 229910017604 nitric acid Inorganic materials 0.000 claims description 4
- 229920002866 paraformaldehyde Polymers 0.000 claims description 4
- 238000001556 precipitation Methods 0.000 claims description 4
- 238000006722 reduction reaction Methods 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- SKYGTJFKXUWZMD-UHFFFAOYSA-N ac1l2n4h Chemical compound [Co].[Co] SKYGTJFKXUWZMD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 150000003891 oxalate salts Chemical class 0.000 claims description 2
- 238000007781 pre-processing Methods 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 1
- 235000013495 cobalt Nutrition 0.000 description 71
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 15
- 239000007788 liquid Substances 0.000 description 13
- 229910052742 iron Inorganic materials 0.000 description 9
- 239000000047 product Substances 0.000 description 7
- -1 and its physics Substances 0.000 description 5
- 239000003054 catalyst Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- ZNCPFRVNHGOPAG-UHFFFAOYSA-L sodium oxalate Chemical compound [Na+].[Na+].[O-]C(=O)C([O-])=O ZNCPFRVNHGOPAG-UHFFFAOYSA-L 0.000 description 5
- 229940039790 sodium oxalate Drugs 0.000 description 5
- 239000005416 organic matter Substances 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 239000000956 alloy Substances 0.000 description 3
- 238000004176 ammonification Methods 0.000 description 3
- 238000009388 chemical precipitation Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000008236 heating water Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- VBIXEXWLHSRNKB-UHFFFAOYSA-N ammonium oxalate Chemical compound [NH4+].[NH4+].[O-]C(=O)C([O-])=O VBIXEXWLHSRNKB-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910000428 cobalt oxide Inorganic materials 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 235000006408 oxalic acid Nutrition 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- HLLSOEKIMZEGFV-UHFFFAOYSA-N 4-(dibutylsulfamoyl)benzoic acid Chemical compound CCCCN(CCCC)S(=O)(=O)C1=CC=C(C(O)=O)C=C1 HLLSOEKIMZEGFV-UHFFFAOYSA-N 0.000 description 1
- 241000165940 Houjia Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229910000914 Mn alloy Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 150000001868 cobalt Chemical class 0.000 description 1
- INPLXZPZQSLHBR-UHFFFAOYSA-N cobalt(2+);sulfide Chemical compound [S-2].[Co+2] INPLXZPZQSLHBR-UHFFFAOYSA-N 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229940039748 oxalate Drugs 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- CADICXFYUNYKGD-UHFFFAOYSA-N sulfanylidenemanganese Chemical compound [Mn]=S CADICXFYUNYKGD-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
-
- 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
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/006—Wet processes
- C22B7/007—Wet processes by acid 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
- C22B23/00—Obtaining nickel or cobalt
- C22B23/04—Obtaining nickel or cobalt by wet processes
- C22B23/0407—Leaching processes
- C22B23/0446—Leaching processes with an ammoniacal liquor or with a hydroxide of an alkali or alkaline-earth metal
-
- 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
- C22B47/0009—Obtaining manganese from spent catalysts
-
- 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
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/006—Wet processes
- C22B7/008—Wet processes by an alkaline or ammoniacal 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
- C22B7/00—Working up raw materials other than ores, e.g. scrap, to produce non-ferrous metals and compounds thereof; Methods of a general interest or applied to the winning of more than two metals
- C22B7/009—General processes for recovering metals or metallic compounds from spent catalysts
-
- 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
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Removal Of Specific Substances (AREA)
Abstract
The invention discloses a method for separating and recovering cobalt and manganese in low-cobalt high-manganese waste by using ammonia-ammonium carbonate, which comprises the steps of pretreating the low-cobalt high-manganese waste to be treated, adding ammonia-ammonium carbonate mixed solution, filtering after the reaction is finished to respectively obtain cobalt-ammonia complex solution and manganese carbonate precipitate, and recovering manganese in the low-cobalt high-manganese waste in the form of manganese carbonate; finally, cobalt is recovered from the cobalt-ammonia complex solution. The method has simple process, high recovery rate of cobalt and manganese, high recovery rate of cobalt up to more than 95%, high recovery rate of manganese up to more than 99%, and high-valued recovery of non-ferrous metal resources.
Description
The application is Application No. 201510839476.9, and the applying date is on November 27th, 2015, and invention and created name is
The divisional application of the application for a patent for invention of " with the method for cobalt and manganese in ammonia-ammonium carbonate separation and recovery high manganese waste material of low cobalt ".
Technical field
The present invention relates to a kind of separation and recovery method of cobalt manganese waste material, and in particular to a kind of ammonia-ammonium carbonate separation and recovery
The method of cobalt and manganese in the high manganese waste material of low cobalt.
Background technology
Containing substantial amounts of cobalt, manganese element in caused useless cobalt-manganese catalyst in PTA productions, wherein cobalt content is about 10 %,
Manganese content is about 20 %.Cobalt is a kind of important strategy metal, and its physics, chemical property are excellent, is production heat-resisting alloy, hard
Alloy, anti-corrosion alloy, the important source material of magnetic alloy and various cobalt salts；And China's cobalt ore resource famine, but the year of cobalt
Consumption figure increases year by year, and domestic cobalt resource can not meet productive consumption demand, and most of cobalt raw material relies on import.Manganese is a kind of
Transition metal, property is hard and crisp, and moist place can aoxidize, and the most important purposes of manganese is manufacture manganese alloy.
At present, both at home and abroad the method for conventional separation and recovery cobalt-manganese catalyst mainly have chemical precipitation method, solvent extraction,
Electrolysis and ion-exchange etc..Chemical precipitation method is easy to operate, technological process is simple, but easily equipment is caused to corrode,
Need to optimize.Solvent extraction can efficiently separate out cobalt, cheap, but organic solvent easily causes to endanger to environment
Evil, and the condition control reacted requires also higher.Electrolysis can reclaim to obtain the high electrolytic cobalt of purity, but with electricity
Solve the defects of liquid is unstable.Ion-exchange can reach rich product and the purpose of purification, storng-acid cation exchange resin tool simultaneously
There is the characteristics of absorption appearance is maximum, and adsorption rate is fast, but ion exchange resin needs regular regeneration, produces a large amount of alkaline waste waters,
Environment is polluted.
On chemical precipitation method, Chinese patent literature CN 1236735A（Application number 98111313.3）Disclose a kind of cobalt
The separation and refining method of Mn mixture, vulcanized sodium will be first added after compound acidolysis and is co-precipitated cobalt manganese, then passes through cobalt, manganese sulphur
The solubility product difference of compound first dissolves manganese, then the cobalt sulfide with mixed-acid dissolution indissoluble.This method can efficiently separate cobalt,
Manganese is simultaneously reclaimed, but acid dissolution consumes a large amount of acid solutions three times, and the discharge of acid solution can cause greatly to pollute to environment.
Chinese patent literature CN 1059241C（Application number 98111506.3）It is high from leftover bits and pieces containing cobalt to disclose one kind
The new technology of effect extraction cobalt/cobalt oxide, including acid is molten, ammonification separation plus alkali are heat sink, absorbs, separating, washing step；It is described to contain cobalt
Leftover bits and pieces includes cobalt, iron, manganese element；The molten processing of acid is leftover bits and pieces is preprocessed or be directly dissolved in sulfuric acid or hydrochloric acid, acid
Solution ph is maintained at 2~3；Ammonification separation be by acid it is molten come clear mixed acid solution add excessive ammonia, keep pH value 8~
9, iron and manganese are separated in the form of hydroxide precipitates from reaction solution in this step；It is in cobalt ammonia complexing to add alkali heat sink
Caustic soda is added in solution based on thing to be heated to seething with excitement, and obtains cobalt oxide.Actual treatment cobalt manganese gives up inventor according to the method described above
During material, the rate of recovery for finding cobalt is only 70%.
The content of the invention
The technical problems to be solved by the invention are to provide that a kind of separation of cobalt from manganese is thorough, the rate of recovery is high, recovery product purity
High separates and recovers the method for cobalt and manganese in the high manganese waste material of low cobalt with ammonia-ammonium carbonate.
The technical scheme for realizing the object of the invention is cobalt and manganese in one kind ammonia-ammonium carbonate separation and recovery high manganese waste material of low cobalt
Method, comprise the following steps：
1. pre-processing, pending low cobalt high manganese waste material acid is dissolved, the pH value of material is less than or equal to 3.5 after control acid is molten,
After molten rear material of the pH value less than or equal to 3. 5 of acid is heated in 70 DEG C~85 DEG C of water-bath, filter；Hydrogen is added into filtrate
Sodium hydroxide solution makes its pH value rise to 4~5, is filtered after standing, and obtained filtrate is pending as digestion solution.
2. preparing ammonia-ammonium carbonate mixed solution, the concentration range of ammonium carbonate is 40~100 g/L in mixed solution, ammoniacal liquor
Concentration range is 50~100 g/L, and the pH value of mixed solution is 9~11.
3. cobalt, manganese separate, 2. ammonia-ammonium carbonate mixing that step is prepared is added in the digestion solution obtained after 1. being filtered to step
Solution obtains reaction solution, and the pH value of reaction solution is 7.5~10.0, and the ratio between amount of material of ammonium carbonate and manganese is 0.9 after addition:
1~2:1, the ratio between amount of material of ammoniacal liquor and cobalt is 10:1~50: 1；Reaction solution reaction 6~15 after addition
Hour.
After reaction terminates, filtering, respectively obtain cobalt ammonia complex solution and manganese carbonate precipitation, in the high manganese waste material of low cobalt manganese with
The form recovery of manganese carbonate.
4. Call Provision, 3. cobalt ammonia complex solution that step is filtrated to get is heated to 70 DEG C~185 DEG C, thrown thereto
Add reducing agent, the ratio between reducing agent and amount of material of cobalt in cobalt ammonia complex solution are 0.8:1~5:1, reaction 15min~
60min；Then lower dropwise addition sodium hydroxide solution or oxalate solution are stirred in the material after terminating to reduction reaction, is added dropwise
20min~60min is reacted afterwards；Reaction filters after terminating, and the washing of precipitate for filtering to obtain obtains cobalt hydroxide or oxalic acid after drying
Cobalt, complete the recovery of cobalt.
Appeal step 1. in used acid be nitric acid, hydrochloric acid or sulfuric acid, cobalt, the material of manganese in sour dosage and cobalt manganese waste material
The ratio between amount be n (H+) : [ n ( Mn ) + n ( Co ) ] = 2 :1~4: 1.
Further, step 1. it is middle with sour dissolved cobalt manganese waste material when, sour pH value used be less than 1.
Above-mentioned steps 3. in 1. filtered to step after add 2. ammonia-ammonium carbonate mixing that step is prepared in obtained digestion solution
After solution obtains reaction solution, reaction 6~15 is small under reaction solution is 150~500 r/min in 20~40 DEG C, mixing speed
When.
4. middle reducing agent is one kind in hydrazine hydrate, sodium borohydride, ethylene glycol or paraformaldehyde to above-mentioned steps.
Further, step 4. in 3. cobalt ammonia complex solution that step is filtrated to get be placed in water-bath be heated to 70
DEG C~85 DEG C, reducing agent is then added, the reducing agent added is hydrazine hydrate, sodium borohydride or paraformaldehyde；Or step is 4.
3. cobalt ammonia complex solution that step is filtrated to get is placed in oil bath pan and is heated to 170 DEG C~185 DEG C, then adds reduction
Agent, the reducing agent added are ethylene glycol.
Further, when step be 4. added dropwise be sodium hydroxide solution when, n（NaOH）：n（Co）=8.5：1~15：1；
When dropwise addition be oxalates when, n（C2O4 2-）：n（Co）=8：1~20：1.
Above-mentioned steps 1. in the pending high manganese waste material of low cobalt cobalt, the mass ratio of manganese be 1:1~1:4.
The present invention has positive effect：（1）The separation and recovery method of the present invention is adapted to all cobalt manganese waste materials, particularly cobalt
Low cobalt high manganese waste material of the manganese ratio 1: 1~4, such as the cobalt-manganese catalyst that given up caused by petroleum industry production PTA, present invention process letter
Single, cost recovery is low, and the rate of recovery of cobalt and manganese is all very high, and the rate of recovery of cobalt can be up to more than 95%, and the rate of recovery of manganese can reach
To more than 99%.
（2）First less than 1 strong acid that the high manganese waste material acid of low cobalt is molten with pH value during present invention pretreatment, acid, which is dissolved, finishes control liquid
The pH value of body is less than or equal to 3.5, heats and filters off the organic matter in the molten rear material that deacidifies, then to the thing after organics removal
Sodium oxide molybdena is hydrogenated with material makes the pH value of liquid rise to 4~5, and the purpose of this regulation pH value is to remove impurity iron, if cobalt manganese waste material
In contain impurity iron, the iron ion after acid is molten can precipitate with hydroxyl from generation, is removed after filtering.The present invention is by impurity iron
Removal is placed on before ammonification step, ensure that the cobalt of separation and recovery and the purity of manganese；And the step of adding organics removal,
It is further ensured that the cobalt of separation and recovery and the purity of manganese.
（3）When present invention processing cobalt ammonia complex is with Call Provision, first cobalt ammonia complex is reduced, trivalent cobalt is reduced to two
Valency cobalt, sodium hydroxide or sodium oxalate or ammonium oxalate are then added into the cobalt ammonia complex of divalence, obtains cobalt sediment.Reducing agent
Addition can destroy the stability of trivalent cobalt ammonia complex, the cobalt ammonia complex after reduction is easier and sodium hydroxide or oxalic acid
Root reacts, and so as to improve the rate of recovery of cobalt, obtained cobalt product purity is high.
（4）2. ammonia-ammonium carbonate mixed solution that the step of the present invention is prepared is cushioning liquid so that anti-when step is reacted 3.
The pH value of system is answered to ensure that reaction is smoothed out in stable scope, the rate of recovery of final products is high；Buffering used is molten in addition
Liquid cost is low, reduces the cost recovery of cobalt manganese waste material.
Embodiment
Cobalt content is less than and is equal to manganese content in the high manganese waste material of heretofore described low cobalt.
（Embodiment 1）
The high manganese waste material of low cobalt handled by the present embodiment is caused useless cobalt-manganese catalyst in PTA productions, and the content of wherein cobalt is
9.872wt %, the content of manganese is 17.12 wt %.
The present embodiment is comprised the following steps with the method for cobalt and manganese in ammonia-ammonium carbonate separation and recovery high manganese waste material of low cobalt：
1. pre-process.The high manganese waste material of 13 grams of low cobalts is taken, 40% nitric acid is added into the reaction vessel for filling the high manganese waste material of low cobalt
The mL of solution 30, after the resolution completely of cobalt manganese waste material, the pH value of liquid is 1.5 after measurement acid is molten.In the dosage and dead catalyst of acid
The ratio between amount of material of cobalt manganese is n (H+) : [ n ( Mn ) + n ( Co ) ] = 2 :1~4: 1.
By molten rear material of the pH value less than 3.5 min of heating water bath 30 in 80 DEG C of water-bath of acid, filter, go to deacidify
Organic matter after molten in material.The pH value of liquid after needing control acid molten before heating water bath, if the pH value of liquid is more than after acid is molten
3.5, acid used is that nitric acid makes its pH value less than 3.5 when adding sour molten waste material thereto, due to the molten rear liquid of acid in the present embodiment
The pH value of body is 1.2, therefore can be directly heated.
5mol/L sodium hydroxide solution is added into the material for eliminate organic matter makes its pH value rise to 4~5（This reality
Apply in example is 4.5）；Filtered after standing 20min, obtained filtrate i.e. digestion solution is pending.Measuring cobalt content in digestion solution is
50.25 g/L, manganese content are 95.75 g/L.If having iron ion in material after acid is molten, iron ion generates hydroxide in this step
Iron precipitates, and is removed after suction filtration from digestion solution.
2. prepare ammonia-ammonium carbonate mixed solution.
Ammonium carbonate is dissolved in ammoniacal liquor, it is stand-by to obtain ammonia-ammonium carbonate mixed solution, the concentration of ammonium carbonate in mixed solution
Scope is 40~100 g/L, and ammonia concn scope is 50~100 g/L, and the pH value of mixed solution is 9~11.The present embodiment
The concentration of ammonium carbonate is 50 g/L in the mixed solution of preparation, and ammonia concn is 60 g/L.
3. cobalt, manganese separate.2. ammonia-ammonium carbonate that step is prepared is slowly added in the digestion solution obtained after 1. being filtered to step
Mixed solution obtains reaction solution, and the pH value of reaction solution is 7.5~10.0, and the ratio between amount of material of ammonium carbonate and manganese is after addition
0.9 :1~2:1, the ratio between amount of material of ammoniacal liquor and cobalt is 10:1~50: 1.Reaction solution exists after addition
30 DEG C, mixing speed be 200 r/min under conditions of react 12 hours.
2. ammonia-ammonium carbonate that step is prepared is slowly added in the digestion solution obtained after 1. filtering to step in the present embodiment to mix
Close solution（Wherein the concentration of ammonium carbonate is 50 g/L, and ammonia concn is 60 g/L）60 mL, the material of ammonium carbonate and manganese after addition
The ratio between amount be 1.3:1, the ratio between amount of material of ammoniacal liquor and cobalt is 10.4: 1.
After reaction terminates, filtering respectively obtains cobalt ammonia complex solution and manganese carbonate precipitation, and manganese carbonate washing of precipitate is dried
Weigh afterwards and obtain 4.6442g, the rate of recovery of manganese is 99.8% in the high manganese waste material of low cobalt, and the purity for the manganese carbonate for reclaiming to obtain is
99.4%。
4. Call Provision.3. cobalt ammonia complex solution that step is filtrated to get is placed in water-bath and is heated to 80 DEG C.To 80
DEG C cobalt ammonia complex solution in add reducing agent 20%~80%（It is 80% in the present embodiment）The mL of hydrazine hydrate 1.00, maintain water
80 DEG C of reaction 15min~60min of bath（It is 20min in the present embodiment）, the cobalt ammonia complex of trivalent is reduced to the cobalt ammonia of divalence
Complex compound.
The reducing agent can also be sodium borohydride, ethylene glycol or paraformaldehyde in addition to above-mentioned hydrazine hydrate used, also
The ratio between amount of material of former agent and cobalt is 0.8:1~5:1.The reducing agent wherein added is hydrazine hydrate, sodium borohydride or more
During polyformaldehyde, 3. cobalt ammonia complex solution that step is filtrated to get is placed in water-bath and is heated to 70 DEG C~85 DEG C, Ran Houjia
Enter reducing agent；When the reducing agent added is ethylene glycol, 3. cobalt ammonia complex solution that step is filtrated to get is placed in oil bath pan
In be heated to 170 DEG C~185 DEG C, then add reducing agent.
Stirring is lower to be added dropwise sodium hydroxide solution, n after addition（NaOH）：n（Co）=8.5:1~15:1.
The mL of sodium hydroxide solution 15, rate of addition 1mL/ that lower dropwise addition concentration is 500 g/L are stirred in the present embodiment
Min, mixing speed are 200 r/min；After 80 DEG C of 30 min of reaction of water-bath are maintained after being added dropwise, filter, filter to obtain sinks
Ethanol wash is first used in shallow lake, then with after distillation water washing, is placed in baking oven and is dried at 70 DEG C~90 DEG C.Ground after drying with mortar
Mill, 100 mesh sieve are crossed, obtain cobalt hydroxide product 2.0189g.The purity of cobalt hydroxide is 99.9%.
The rate of recovery for being computed cobalt is 99.8%.
（Embodiment 2）
Remaining is same as Example 1 for the separation and recovery method of cobalt and manganese in the cobalt manganese waste material of the present embodiment, and difference is：
After the cobalt ammonia complex of step 4. middle trivalent is reduced to the cobalt ammonia complex of divalence, stir it is lower sodium oxalate solution is added dropwise,
Add rear n（C2O4 2-）：n（Co）=8:1~20:1.
Sodium oxalate solution 150 mL, the rate of addition 20mL/min that concentration is 50g/L, stirring speed are added dropwise in the present embodiment
Spend for 500 r/min.
Except the sodium oxalate solution described in the present embodiment, ammonium oxalate can also be used to substitute sodium oxalate.
Cobalt oxalate 3.1794g is obtained after drying, the rate of recovery of cobalt is 99.5 %, and the purity of cobalt oxalate is 99.2%.Cobalt manganese gives up
Cobalt in material is recycled in the form of cobalt oxalate.
（Embodiment 3）
Remaining is same as Example 1 for the separation and recovery method of cobalt and manganese in the cobalt manganese waste material of the present embodiment, and difference is：
When step pre-processes 1., 10 % hydrochloric acid solution 44mL is added into the reaction vessel for filling cobalt manganese waste material, treats that cobalt manganese gives up
After material resolution completely, the pH value of liquid is 4.2 after measurement acid is molten.To acid it is molten after liquid in add 10% hydrochloric acid to pH decline
To less than 3.5, be then transferred to the min of heating water bath 30 in 80 DEG C of water-bath, filter, go to deacidify it is molten after it is organic in material
Thing.
（Embodiment 4）
Remaining is same as Example 1 for the separation and recovery method of cobalt and manganese in the cobalt manganese waste material of the present embodiment, and difference is：
When step pre-processes 1., 30 % sulfuric acid solution 25mL is added into the reaction vessel for filling cobalt manganese waste material, treats that cobalt manganese gives up
After material resolution completely, the pH value of liquid is 1.7 after measurement acid is molten.Liquid of the acid after molten is transferred to 80 DEG C of water-bath reclaimed water
Bath 30 min of heating, are filtered, go to deacidify it is molten after organic matter in material.
（Embodiment 5）
Remaining is same as Example 1 for the separation and recovery method of cobalt and manganese in the cobalt manganese waste material of the present embodiment, and difference is：
Step 3. in 1. filtered to step after be slowly added to 2. ammonia-ammonium carbonate mixed solution that step is prepared in obtained digestion solution
Reaction solution is obtained, the ratio between amount of material of ammonium carbonate and manganese is 2 after addition:1, the ratio between amount of material of ammoniacal liquor and cobalt is 50
: 1.Reaction solution reacts 6 hours under conditions of being 500 r/min in 40 DEG C, mixing speed after addition.
After reaction terminates, filtering respectively obtains cobalt ammonia complex solution and manganese carbonate precipitation, and manganese carbonate washing of precipitate is dried
Weigh afterwards and obtain 4.6676g, the rate of recovery of manganese is 99.9% in the high manganese waste material of low cobalt, and the purity for the manganese carbonate for reclaiming to obtain is
98.5%。
4. step obtains cobalt hydroxide product 1.9926g.The purity of cobalt hydroxide is 99.7%.
The rate of recovery for being computed cobalt is 98.3 %.
Claims (4)
- A kind of 1. method of cobalt and manganese in ammonia-ammonium carbonate separation and recovery high manganese waste material of low cobalt, it is characterised in that including following step Suddenly：1. pre-processing, pending low cobalt high manganese waste material acid is dissolved, the pH value of material is less than or equal to 3.5 after control acid is molten, After molten rear material of the pH value less than or equal to 3. 5 of acid is heated in 70 DEG C~85 DEG C of water-bath, filter；Hydrogen is added into filtrate Sodium hydroxide solution makes its pH value rise to 4~5, is filtered after standing, and obtained filtrate is pending as digestion solution；2. preparing ammonia-ammonium carbonate mixed solution, the concentration range of ammonium carbonate is 40~100 g/L in mixed solution, ammonia concn Scope is 50~100 g/L, and the pH value of mixed solution is 9~11；3. cobalt, manganese separate, 2. ammonia-ammonium carbonate mixed solution that step is prepared is added in the digestion solution obtained after 1. being filtered to step Reaction solution is obtained, the pH value of reaction solution is 7.5~10.0, and the ratio between amount of material of ammonium carbonate and manganese is 0.9 after addition: 1 ~2:1, the ratio between amount of material of ammoniacal liquor and cobalt is 10:1~50: 1；Reaction solution is 20~40 after addition DEG C, mixing speed be 150~500 r/min under react 6~15 hours；After reaction terminates, filtering, cobalt ammonia complex solution and manganese carbonate precipitation are respectively obtained, manganese is with carbonic acid in the high manganese waste material of low cobalt The form recovery of manganese；4. Call Provision, 3. cobalt ammonia complex solution that step is filtrated to get is placed in water-bath and is heated to 70 DEG C~85 DEG C, to Reducing agent is wherein added, the reducing agent added is one kind in hydrazine hydrate, sodium borohydride or paraformaldehyde, or by step 3. mistake The cobalt ammonia complex solution that filter obtains, which is placed in oil bath pan, is heated to 170 DEG C~185 DEG C, then adds reducing agent, is added Reducing agent is ethylene glycol；The ratio between amount of material of cobalt is 0.8 in reducing agent and cobalt ammonia complex solution:1~5:1, reaction 15min~60min；Then lower dropwise addition sodium hydroxide solution or oxalate solution are stirred in the material after terminating to reduction reaction, what it is when dropwise addition is During sodium hydroxide solution, n（NaOH）：n（Co）=8.5：1~15：1；When dropwise addition be oxalates when, n（C2O4 2-）：n（Co）= 8：1~20：1；20min~60min is reacted after being added dropwise；Reaction is filtered after terminating, and the washing of precipitate for filtering to obtain is dried After obtain cobalt hydroxide or cobalt oxalate, complete the recovery of cobalt.
- 2. the method for cobalt and manganese, its feature according to claim 1 in ammonia-ammonium carbonate separation and recovery high manganese waste material of low cobalt It is：Step 1. in used acid be nitric acid, hydrochloric acid or sulfuric acid, cobalt in sour dosage and cobalt manganese waste material, manganese material amount it Than for n (H+) : [ n ( Mn ) + n ( Co ) ] = 2 :1~4: 1.
- 3. the method for cobalt and manganese, its feature according to claim 1 in ammonia-ammonium carbonate separation and recovery high manganese waste material of low cobalt It is：Step 1. it is middle with sour dissolved cobalt manganese waste material when, sour pH value used be less than 1.
- 4. separate and recover the side of cobalt and manganese in the high manganese waste material of low cobalt with ammonia-ammonium carbonate according to one of claims 1 to 3 Method, it is characterised in that：Step 1. in the pending high manganese waste material of low cobalt cobalt, the mass ratio of manganese be 1:1~1:4.
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| GB1348031A (en) * | 1971-05-13 | 1974-03-13 | Roy T K | Process for recovery of nickel and cobalt |
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| GB751866A (en) * | 1953-12-21 | 1956-07-04 | Chemical Construction Corp | Improvements in or relating to method of recovering metals |
| GB1348031A (en) * | 1971-05-13 | 1974-03-13 | Roy T K | Process for recovery of nickel and cobalt |
| CN1651584A (en) * | 2005-02-06 | 2005-08-10 | 金川集团有限公司 | Production method of dentritic morphology nickel powder |
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