CN103757374A - Leaching method of waste battery electrode mixed material - Google Patents

Leaching method of waste battery electrode mixed material Download PDF

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Publication number
CN103757374A
CN103757374A CN201310736572.1A CN201310736572A CN103757374A CN 103757374 A CN103757374 A CN 103757374A CN 201310736572 A CN201310736572 A CN 201310736572A CN 103757374 A CN103757374 A CN 103757374A
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China
Prior art keywords
leaching
acid
mixing material
sulfuric acid
nitric acid
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CN201310736572.1A
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Chinese (zh)
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龙炳清
方绪坤
周讯
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Sichuan Normal University
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Sichuan Normal University
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Priority to CN201310736572.1A priority Critical patent/CN103757374A/en
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    • 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

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Abstract

The invention provides a leaching method of a waste battery electrode mixed material, which comprises the following steps: adding an electrode mixed material subjected to roasting pretreatment separated from waste batteries and cocoanut shell flour into a pressure-resistant sulfuric-acid/nitric-acid-corrosion-resistant reaction kettle, adding a sulfuric acid-nitric acid mixed solution, and carrying out agitation leaching under sealed conditions.

Description

The leaching method of refuse battery electrode mixing material
Technical field
The present invention relates to a kind of leaching method of refuse battery electrode mixing material.
Background technology
Battery is widely used in the fields such as illumination, communication, traffic.Battery will produce a large amount of refuse batteries after using and scrapping.Owing to containing plurality of heavy metal in battery, if abandon into environment, will environment be produced to very large direct and potential hazard.Refuse battery electrode mixing material is nickeliferous, cobalt, lithium, copper, aluminium, cadmium, rare earth and Mn mainly, has very much a recovery value.The technique that reclaims at present the valuable metals such as nickel, cobalt, lithium, copper, cadmium and rare earth from refuse battery electrode mixing material mainly contains thermal process and wet processing.The product that thermal process obtains is alloy material, nickel, cobalt, lithium, copper, cadmium and rare earth etc. that very difficult acquisition is purer.Wet processing becomes more readily available purer nickel, cobalt, lithium, copper, cadmium and rare earth etc.Leaching is a requisite process in wet processing.The leaching method of refuse battery electrode mixing material mainly contains hydrochloric acid leaching process, sulfuric acid leaching, nitric acid lixiviation process and nitration mixture (sulfuric acid adds nitric acid) lixiviation process at present.Hydrochloric acid leaching process, equipment corrosion is large, the large and contaminate environment of acid mist generation.The reductive agent agent (as hydrogen peroxide etc.) that sulfuric acid leaching consumption is more expensive.The nitric acid consumption of nitric acid lixiviation process is large, and can produce a large amount of oxynitride, contaminate environment.All there is the problem that improves how economically leaching velocity, raising metal leaching rate, reduces acid consumption and other supplementary product onsumption in all wet processings.Although nitric acid processing industry pure oxygen lixiviation process and nitration mixture processing industry pure oxygen lixiviation process have solved the problems referred to above preferably, but leaching plant is more complicated, and the required industrial pure oxygen amount of refuse battery leaching is little, refuse battery is processed enterprise, and manufacture pure oxygen is personal uneconomical on the spot, and the storage of industrial pure oxygen, transportation and use are cumbersome.Development equipment corrosion is little, leaching velocity is fast, leaching yield is high, acid consumes and other supplementary product onsumption is low, easy to use, the leaching method of the refuse battery electrode mixing material of basic non-environmental-pollution has larger practical value.
Summary of the invention
The problem leaching for current refuse battery electrode mixing material, the object of the invention is to find a kind of metal leaching rate high, leaching velocity is fast, leaching yield is high, acid consumption and other supplementary product onsumption are low, easy to use, need not expensive reductive agent, the leaching method of the refuse battery electrode mixing material of basic non-environmental-pollution, it is characterized in that by electrode mixing material isolated from refuse battery and that obtain through roasting pretreatment and≤coconut shell powder of 1.5mm adds withstand voltage, in the reactor of resistance to sulfuric acid and nitric acid corrosion, the mixing solutions that adds sulfuric acid and nitric acid, and carry out in confined conditions agitation leach.After leaching finishes, carry out liquid-solid separation, obtain required infusion solution.Temperature of reaction is 50 ℃~80 ℃, and the sulfuric acid starting point concentration of leaching is 1mol/L~4mol/L, and the starting point concentration of nitric acid is that 5g/L~10g/L extraction time is 2h~4h, and leaching process stirs, and stirring velocity is 30r/min~120r/min.Sulphuric acid is to add 110%~140% of sulfuric acid theoretical consumption that in the electrode mixing material of reaction vessel, all metals leach.The add-on of coconut shell powder is counted 60%~75% of nickel in electrode mixing material, cobalt and manganese total mass with butt.
The object of the present invention is achieved like this: airtight and have under the condition that coconut shell powder and nitric acid exists, the refuse battery electrode mixing material of sulfuric acid leaching after roasting pretreatment is when (metallic element in material is oxide form), and following main chemical reactions occurs leaching process:
NiO?+?H 2SO 4?=?NiSO 4?+?H 2O
CuO?+?H 2SO 4?=?CuSO 4?+?H 2O
Al 2O 3?+?3H 2SO 4?=?Al 2(SO 4) 3?+?3H 2O
Li 2O?+?H 2SO 4?=?Li 2SO 4?+?H 2O
CoO?+?H 2SO 4?=?CoSO 4?+?H 2O
CdO?+?H 2SO 4?=?CdSO 4?+?H 2O
Re 2O 3?+?3H 2SO 4?=?Re 2(SO 4) 3?+?3H 2O
nC 6H 10O 5?+?nH 2SO 4?=n(C 5H 11O 5)HSO 4
n(C 5H 11O 5)HSO 4?+?nH 2O?=?nC 6H 12O 6?+?nH 2SO 4
C 6H 12O 6?+?8HNO 3?=?8NO?+?6CO 2?+?10H 2O
nC 6H 10O 5?+?8nHNO 3?=?8nNO?+?6nCO 2?+?9nH 2O
3Ni 2O 3?+?6H 2SO 4?+?2NO?=?6NiSO 4?+?2HNO 3?+?5H 2O
3Co 2O 3?+?6H 2SO 4?+?2NO?=?6CoSO 4?+?2HNO 3?+?5H 2O
3Mn 2O 3?+?6H 2SO 4?+?2NO?=?6MnSO 4?+?2HNO 3?+?5H 2O
Ni 2o 3, Co 2o 3and Mn 2o 3total reaction be:
12nNi 2O 3?+?nC 6H 10O 5?+?24nH 2SO 4?=?24nNiSO 4?+?6nCO 2?+?29nH 2O
12nCo 2O 3?+?nC 6H 10O 5?+?24nH 2SO 4?=?24nCoSO 4?+?6nCO 2?+?29nH 2O
12nMn 2O 3?+?nC 6H 10O 5?+?24nH 2SO 4?=?24nMnSO 4?+?6nCO 2?+?29nH 2O
Other organism in coconut shell powder also generates NO, CO with nitric acid reaction 2and H 2o, the NO of generation and Ni 2o 3, Co 2o 3and Mn 2o 3by previous reaction, generate NiSO 4, CoSO 4, MnSO 4, HNO 3and H 2o.
Because the speed of response of nitric acid and coconut shell powder is very fast, the NO of generation and Ni 2o 3, Co 2o 3and Mn 2o 3reaction also very fast, accelerate thus whole leaching process, and realize Ni 2o 3, Co 2o 3and Mn 2o 3leach more completely.NO can thoroughly destroy the laminate structure of high oxide in electrode mixing material, improves the leaching yield of valuable metal.
With respect to existing method, outstanding advantages of the present invention is to adopt coconut shell powder to make reductive agent, and nitric acid is made to leach accelerator and leached refuse battery electrode mixing material, and speed of response is fast, and such as reaction acidity is lower, and the consumption of sulfuric acid and reductive agent is little, and coconut shell powder is cheap; In electrode mixing material, the laminate structure of high oxide is destroyed thoroughly, can improve metal leaching rate; In leach liquor subsequent disposal, do not need to neutralize a large amount of acid, cost is lower; The waste amount producing in leach liquor subsequent disposal is few, has reduced pollution abatement costs, has obvious economic benefit and environmental benefit; Process is carried out in confined conditions, the environmental pollution of having avoided NO to overflow and produce.
specific implementation method
embodiment 1: by 100g refuse battery electrode mixing material (nickeliferous 20.5%, cobalt 20.3%, lithium 8.4%, aluminium 2.2%, copper 2.5%, cadmium 2.3%, manganese 4.9%, rare earth 5.7%) and≤to add volume be in the lining titanium pressure reaction still of 2L to 1.5mm coconut shell powder 27.5g, adding sulfuric acid concentration is the mixed acid solution 1170ml that 1.5mol/L, concentration of nitric acid are 5g/L, at 50 ℃~60 ℃, 4.0h is leached in airtight stirring (stirring velocity 80r/min), after leaching finishes, carry out liquid-solid separation, obtain 1100ml infusion solution (not containing leached mud washing water).The leaching yield of nickel, cobalt, lithium, copper, cadmium, manganese, aluminium, rare earth be respectively 99.2%, 99.2%, 99.5%, 99.3%, 99.2%, 99.2%, 98.6% and 8.3%(by entering nickel in infusion solution and leached mud washings, cobalt, lithium, copper, cadmium, manganese, aluminium, rare earth, calculate).
Embodiment 2: by 500g refuse battery electrode mixing material (nickeliferous 20.5%, cobalt 20.3%, lithium 8.4%, aluminium 2.2%, copper 2.5%, cadmium 2.3%, manganese 4.9%, rare earth 5.7%) and≤to add volume be in the lining titanium pressure reaction still of 5L to 1.5mm coconut shell powder 170g, adding sulfuric acid concentration is the mixed acid solution 3500ml that 3.0mol/L, concentration of nitric acid are 10g/L, at 70 ℃~80 ℃, 2h is leached in airtight stirring (stirring velocity 60r/min), after leaching finishes, carry out liquid-solid separation, obtain 3200ml infusion solution (not comprising leached mud washing water).The leaching yield of nickel, cobalt, lithium, copper, cadmium, manganese, aluminium, rare earth be respectively 99.3%, 99.4%, 99.6%, 99.2%, 99.3%, 99.4%, 99.0% and 5.8%(by entering nickel in infusion solution and leached mud washings, cobalt, lithium, copper, cadmium, manganese, aluminium, rare earth, calculate).

Claims (1)

1. the leaching method of a refuse battery electrode mixing material, be characterised in that by electrode mixing material isolated from refuse battery and that obtain through roasting pretreatment and≤coconut shell powder of 1.5mm adds withstand voltage, in the reactor of resistance to sulfuric acid and nitric acid corrosion, the mixing solutions that adds sulfuric acid and nitric acid, and carry out in confined conditions agitation leach, after finishing, leaching carries out liquid-solid separation, obtain required infusion solution, temperature of reaction is 50 ℃~80 ℃, the sulfuric acid starting point concentration leaching is 1mol/L~4mol/L, the starting point concentration of nitric acid is that 5g/L~10g/L extraction time is 2h~4h, leaching process stirs, stirring velocity is 30r/min~120r/min, sulphuric acid is to add 110%~140% of sulfuric acid theoretical consumption that in the electrode mixing material of reaction vessel, all metals leach, the add-on of coconut shell powder is counted nickel in electrode mixing material with butt, 60%~75% of cobalt and manganese total mass.
CN201310736572.1A 2013-12-29 2013-12-29 Leaching method of waste battery electrode mixed material Pending CN103757374A (en)

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Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101619394A (en) * 2009-06-23 2010-01-06 四川师范大学 Method for leaching anode and cathode mixed material of waste lithium nickel manganese cobalt battery
CN102030375A (en) * 2010-10-29 2011-04-27 北京矿冶研究总院 Method for preparing lithium cobaltate by directly using failed lithium ion battery

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101619394A (en) * 2009-06-23 2010-01-06 四川师范大学 Method for leaching anode and cathode mixed material of waste lithium nickel manganese cobalt battery
CN102030375A (en) * 2010-10-29 2011-04-27 北京矿冶研究总院 Method for preparing lithium cobaltate by directly using failed lithium ion battery

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Application publication date: 20140430