CN108808033A - Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery - Google Patents

Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery Download PDF

Info

Publication number
CN108808033A
CN108808033A CN201810556643.2A CN201810556643A CN108808033A CN 108808033 A CN108808033 A CN 108808033A CN 201810556643 A CN201810556643 A CN 201810556643A CN 108808033 A CN108808033 A CN 108808033A
Authority
CN
China
Prior art keywords
electrode material
solution
waste
preparing
supercapacitor
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
CN201810556643.2A
Other languages
Chinese (zh)
Other versions
CN108808033B (en
Inventor
周莹杰
程韦豪
王卫
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.)
Nanjing University of Information Science and Technology
Original Assignee
Nanjing University of Information Science and Technology
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 Nanjing University of Information Science and Technology filed Critical Nanjing University of Information Science and Technology
Priority to CN201810556643.2A priority Critical patent/CN108808033B/en
Publication of CN108808033A publication Critical patent/CN108808033A/en
Application granted granted Critical
Publication of CN108808033B publication Critical patent/CN108808033B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/52Reclaiming serviceable parts of waste cells or batteries, e.g. recycling
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/30Electrodes characterised by their material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/30Electrodes characterised by their material
    • H01G11/32Carbon-based
    • H01G11/44Raw materials therefor, e.g. resins or coal
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/30Electrodes characterised by their material
    • H01G11/46Metal oxides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/13Energy storage using capacitors
    • 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
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/84Recycling of batteries or fuel cells

Abstract

The invention discloses a method for preparing a supercapacitor electrode material by using a waste zinc-manganese battery, wherein the supercapacitor electrode material comprises a Zn-Mn blended oxide nano electrode material and a composite nano electrode material, zn and Mn elements are respectively recovered from the waste zinc-manganese battery to obtain Mn (NO) 3 ) 2 Solution and ZnCl 2 A solution; then using Mn (NO) 3 ) 2 Solution and ZnCl 2 The solution is used for preparing Zn-Mn blended oxide nano electrode materials and composite nano electrode materials respectively. The invention not only can solve the problem of waste batteriesThe environmental protection problem brought can realize the recycling of waste resources simultaneously. Realizes the reutilization of waste resources from the dual angles of environmental protection and energy development.

Description

Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery
Technical Field
The invention relates to the technical field of waste battery recycling, in particular to a method for preparing a supercapacitor electrode material by using a waste zinc-manganese battery.
Background
Since the 21 st century, the continuous development of the electronic industry has made batteries become indispensable products in life and production, wherein 80 ten thousand tons of automobile batteries, 19 ten thousand tons of industrial batteries and 16 ten thousand tons of portable batteries are put on the market every year in the european union alone, the production of waste batteries is also increased year by year, and the average recovery rate of the waste batteries is only 13.6%. Among the consumable portable batteries, the zinc-manganese battery (including acidic and alkaline batteries) accounts for 90.8%, and since these waste batteries are not rechargeable, they are discarded after rapidly consuming the electricity, and a large amount of solid waste, including Zn, mn and other heavy metals, is generated, which causes serious pollution to the environment where human beings live. At present, china becomes the biggest battery producing country and consumer country in the world, and is also the biggest waste battery producing country. The waste portable batteries are generally treated as household garbage to be landfilled and burned, and the waste batteries enter the soil to threaten the ecological environment and human health and cause a great deal of waste of resources and energy. Therefore, it is important to recycle and recycle the waste batteries in a simple manner. At present, people have developed high-efficiency recycling methods with simple processes and low cost, and the new methods not only have positive influence on the environment, but also can prepare advanced functional materials. For example, tu et al recovered Zn-Mn waste batteries to prepare high efficiency nano-adsorbent for removing toxic metals; hu et al prepared Zn-Mn ferrite; qu et al prepared a high efficiency ZnMnO photocatalyst for bisphenol A degradation; preparation of LiMn by Chen et al 2 O 4 The material is used for the lithium battery positive electrode material. Besides, the recovered Zn-Mn waste battery can be used as an electrode material for preparing a super capacitor: ali, etc 5 Obtained by combining leaching and electrolytic deposition techniquesThe obtained nano flower-like manganese dioxide is used for preparing a super capacitor, the good circulation stability is shown, and the capacitance can reach 294F/g under the sweeping speed of 10 mV/s; deng et al physically mix waste battery powder and graphene oxide or reduced graphene oxide to prepare a manganese dioxide/graphene nano electrode material for a super capacitor to show high specific capacitance. From the above, it can be known that Zn and Mn recovered from waste batteries can be used as raw materials of electrode materials of supercapacitors.
In addition, activated carbon materials prepared from sustainable biomass materials are receiving attention from researchers due to their advantages of abundant raw materials, simple preparation, low cost, and wide working temperature range. The rice straw, the wheat straw, the corn stalk, the peanut shell and the like are used as agricultural byproducts, and the agricultural byproducts are rich in resources and have reproducibility and cleanness. Besides a small part of the biological materials are used as feed or fertilizer, most of the biological materials are thrown away as fuel or waste, the utilization rate is low, and not only is the natural resources greatly wasted, but also the environment is polluted. The crop byproducts can generate a novel environment-functional biochar through a series of processes such as high-temperature calcination, carbonization and the like, and the surface of the biochar has rich functional groups and a pore-size structure. The composite material mainly comprises carboxyl, phenolic hydroxyl, carbonyl, lactone, pyrone, anhydride and the like, and can fully utilize the surface functional group and the pore-size structure of biochar to prepare an excellent supercapacitor electrode material, thereby realizing double recycling of waste batteries and crop byproducts.
Disclosure of Invention
The invention aims to provide a method for preparing a supercapacitor electrode material by using a waste zinc-manganese battery, aiming at the defects in the prior art.
The purpose of the invention is realized by the following technical scheme:
a method for preparing a supercapacitor electrode material by using a waste zinc-manganese battery, wherein the supercapacitor electrode material comprises a Zn-Mn blended oxide nano electrode material and a composite nano electrode material, and the method specifically comprises the following steps:
step 1, respectively recovering Zn and Mn elements from waste zinc-manganese batteries to obtain Mn (NO) 3 ) 2 Solution and ZnCl 2 A solution;
step 2, using Mn (NO) 3 ) 2 Solution and ZnCl 2 Respectively preparing a Zn-Mn blended oxide nano electrode material and a composite nano electrode material by using the solution:
1) Preparing a Zn-Mn blended oxide nano electrode material:
mixing Mn (NO) 3 ) 2 Solution and ZnCl 2 Mixing the solution with 4:1-16 in a molar ratio, adding urea to adjust the pH value of the mixed solution to be neutral, adding ethanol into the mixed solution, wherein the volume of the ethanol and the volume of the mixed solution are 1.2-2, reacting at 100-180 ℃ for 12-24 h, fully washing a generated solid product with a deionized water and ethanol mixed solution with the volume ratio of 1 (0.3-3), filtering out precipitates, and drying to obtain the Zn-Mn blended oxide nano electrode material;
2) Preparing a composite nano electrode material: mixing charcoal powder according to a mass ratio of 1:0.5-3 to ZnCl 2 Fully soaking in the solution, filtering out precipitates, calcining for 2-6 hours at 700-1000 ℃ under an inert atmosphere, fully washing with HCl with the concentration of 0.1-0.5mol/L to remove residual oxides in the biochar, washing with deionized water and drying to obtain activated biochar; then carrying out oxidation modification treatment on the activated charcoal to obtain surface oxidation modified charcoal; adding surface oxidation modified charcoal into Mn (NO) 3 ) 2 Mixing and fully soaking in the solution, adding organic solvent and ligand, ultrasonically pulverizing and emulsifying, thermally reacting at 120-200 deg.C for 12-24 h to obtain solid powder 2 Or calcining 2-8 h at 700-1000 ℃ under Ar atmosphere to obtain the composite nano electrode material.
In a further design scheme of the invention, in the step 1, the specific steps of respectively recovering Zn and Mn elements from the waste zinc-manganese battery are as follows: crushing the waste zinc-manganese dry batteries by adopting a mechanical crushing method, and respectively collecting a waste positive Mn compound and a waste negative Zn compound;
ultrasonically cleaning and filtering the Mn compound until the filtrate is neutral to obtain primary powder, and calcining the primary powder in a muffle furnace at 250-500 ℃ for 2-5 hours to obtain a recovered Mn compound; using 0.5-3 mol/L HNO 3 Solution with 30wt% H 2 O 2 Co-dissolving the calcined Mn compound and filtering the filtrate to obtain recovered Mn (NO) 3 ) 2 A solution;
putting the Zn compound into 0.5-3 mol/L HCl solution, stirring until the Zn compound is dissolved, and obtaining the recovered ZnCl 2 And (3) solution.
In a further design scheme of the invention, the preparation of the charcoal powder in the step 2 comprises the following specific steps: pulverizing peanut shells, corncobs, rice husks and wheat straws by a pulverizer, fully washing with deionized water to remove dust on the surface, drying in an oven, calcining at 400-550 ℃ in an inert atmosphere for 2-6 h, and fully grinding to obtain the charcoal powder.
In a further design scheme of the invention, the specific steps of carrying out oxidation modification treatment on the activated biochar in the step 2 are as follows: mixing activated charcoal with concentrated H 2 SO 4 Mixing with active biochar and concentrated H 2 SO 4 In a ratio of about 0.1g:10-50 mL. Cooling at 0-5 deg.C, adding KMnO 4 And NaNO 3 The mass ratio of the two is 1 (0.1-9), the reaction is carried out at the temperature of 40-80 ℃ for 0.5-5H, the mixture is diluted by deionized water after being cooled, and H is dripped dropwise 2 O 2 And standing until the mixture turns golden yellow or earthy yellow, and centrifugally washing and separating solid powder to obtain the biochar with the surface subjected to oxidation modification.
In a further design scheme of the invention, the ligand in the step 2 is any one of terephthalic acid, trimesic acid, p-xylylenediamine, trimethylamine, 1-methylimidazole and benzimidazole.
In a further design scheme of the invention, the organic solvent in the step 2 is one or a mixture of any two of methanol, ethanol, ethylene glycol, N-octanol and N, N-dimethylformamide.
The invention has the following outstanding advantages:
the invention provides a method for preparing a high-performance supercapacitor electrode material by recycling waste batteries and agricultural and forestry wastes. The method comprises the steps of firstly recovering Mn and Zn metal elements from waste batteries as precursors to synthesize a nano porous super capacitor electrode material, and then compounding the recovered Mn and Zn metal elements with biochar derived from agricultural and forestry waste to obtain a high-performance super capacitor electrode material, so that the environmental protection problem brought by the waste batteries can be solved, and the recycling rate of agricultural and forestry waste resources can be realized to a certain extent. The waste resources are recycled from the dual aspects of environmental protection and energy development. The electrode material obtained by the invention has the advantages of higher specific surface area, better energy storage effect and easy operation of the preparation process.
Drawings
FIG. 1 is a flow chart of a method for preparing an electrode material of a supercapacitor by using a waste zinc-manganese battery in example 2;
FIG. 2 is a cyclic voltammogram of the Zn-Mn blended oxide nanoelectrode of example 1;
FIG. 3 is a charge and discharge curve of the Zn-Mn blended oxide nanoelectrode in example 1;
FIG. 4 is a cyclic voltammogram of the composite nanoelectrode material of example 2;
FIG. 5 is a charge and discharge curve of the composite nanoelectrode material in example 2.
Detailed Description
The invention is further explained below with reference to the drawings and examples.
Example 1
The method for preparing the Zn-Mn blended oxide nano electrode material by utilizing the waste zinc-manganese battery specifically comprises the following steps:
step 1, respectively returning from the waste zinc-manganese batteriesCollecting Zn and Mn elements to obtain Mn (NO) 3 ) 2 Solution and ZnCl 2 A solution;
the method comprises the steps of crushing waste zinc-manganese dry batteries by adopting a mechanical crushing method, and respectively collecting waste positive Mn compounds and waste negative Zn compounds. And (3) filtering the Mn compound by adopting ultrasonic cleaning until the filtrate is neutral to obtain primary powder, and calcining the primary powder in a muffle furnace at 400 ℃ for 3 hours to obtain the recovered Mn compound. Then, 60mL of 1 mol/L HNO was used 3 With 10 mL 30wt% H 2 O 2 Dissolving the calcined Mn compound together, and filtering to obtain filtrate, i.e. the recovered Mn (NO) 3 ) 2 And (3) solution.
For the Zn collected, the clear solution was first washed with a large amount of deionized water, then weighed, 0.2g was taken, 0.5M HCl solution was added dropwise thereto and stirred until dissolved and filtered, and the filtrate was taken to obtain ZnCl 2 And (3) solution.
Step 2, using Mn (NO) 3 ) 2 Solution and ZnCl 2 Respectively preparing the Zn-Mn blended oxide nano electrode material by using the solution:
20mL of Mn (NO) 3 ) 2 Solution and ZnCl 2 And (2) blending the solutions, adding urea until the pH value of the solution is neutral, then adding ethanol until the total solution amount is 60mL, reacting at 120 ℃ for 24 h, and fully washing, filtering and drying precipitates by using deionized water and ethanol according to the volume ratio of 1:3 to obtain the Zn-Mn blended oxide nano electrode material.
Uniformly mixing the Zn-Mn blended oxide with acetylene black and Polyvinylidene Fluoride (PVDF) in a mass ratio of 7 4 As an electrolyte, ag/AgCl is used as a reference electrode, pt wires are used as a counter electrode, a cyclic voltammetry characteristic curve and constant current charge-discharge performance under different current densities are represented, and detailed electrochemical performances are shown in figures 2 and 3, so that Zn-Mn blended nano oxide recovered from waste batteries shows better capacitance performance, and the nano oxide has better capacitance performance as a super capacitor electrode material as shown in the cyclic voltammetry curve of figure 2The multiplying power of the capacitor can reach 135 mF/cm from the constant current charge-discharge curve 2
Example 2
In this example, mn recovered from waste batteries is compounded with biochar derived from corncobs, and the obtained nanocomposite is used as a supercapacitor electrode, referring to fig. 1, the specific embodiment is as follows:
first, mn (NO) was obtained from the waste batteries by the method of example 1 3 ) 2 Solution and ZnCl 2 Solution, wherein Zn is weighed.
Secondly, taking the agricultural and sideline product corncob, crushing the corncob into small particles, washing the corncob with a large amount of deionized water to remove dust, ultrasonically washing the corncob with 5 wt% HCl to remove soluble impurities, washing the corncob to be neutral, and drying the corncob. Then placing the mixture in a tube furnace at N 2 Pre-calcining at 450 deg.c to obtain charcoal powder. Reacting ZnCl 2 Soaking the solution in 0.5 g charcoal powder, evaporating to remove excessive water, oven drying, and placing in N 2 Calcining 4 h in a tubular furnace in an atmosphere, fully washing with 0.5mol/L HCl of 80 mL to remove residual oxides in the biochar, washing with deionized water, and drying to obtain the activated biochar.
Then, znCl is put into 2 The treated activated biochar is concentrated H with 0.1g and 10 mL 2 SO 4 Mixing well, placing in ice water for cooling, then slowly adding 0.2g KMnO 4 ,0.1 g NaNO 3 Reacting at 60 deg.C for 3H, cooling, diluting with deionized water, and dripping H drop by drop 2 O 2 And standing until the mixture turns golden yellow, and then centrifugally washing to obtain the biochar with the surface subjected to oxidation modification.
Further, mn (NO) recovered from waste batteries is taken 3 ) 2 The solution 20mL and 0.1g surface oxidation modified biochar are fully soaked and mixed, 20mL of ethylene glycol and 20mL of ethanol are added, ligand terephthalic acid is added, ultrasonic crushing and emulsification are carried out, the obtained product is placed in a reaction kettle to react at 150 ℃ for 24 h, and the obtained product is mixed and dissolved by ethanol and waterAfter washing, the mixture was dried in a vacuum oven at 80 ℃ overnight and then N 2 Or calcining 4 h in Ar at 800 ℃ to obtain the composite nano electrode material finally.
And finally, uniformly mixing the composite nano electrode material with acetylene black and Polyvinylidene Fluoride (PVDF) according to the mass ratio of 7 4 As electrolyte, hg/HgO as reference electrode, znCl 2 The treated biochar is a counter electrode, an asymmetric capacitor is prepared, a cyclic voltammetry characteristic curve and constant current charge and discharge performance of the capacitor under different current densities are represented, and a cyclic voltammetry curve and a charge and discharge curve thereof are shown in fig. 3. The discovery of Mn element and ZnCl recovered from waste batteries 2 When the composite nano material obtained after the activated and surface oxidation modified biochar composite is treated as the anode and the activated biochar is the cathode, the assembled water system asymmetric super capacitor shows better capacitance performance, and the energy density is about 31.3 Wh.g under the current density of 1A/g -1 The power density is about 834W.g -1
The above are preferred embodiments of the present invention, and all changes made according to the technical solutions of the present invention that produce functional effects do not exceed the scope of the technical solutions of the present invention belong to the protection scope of the present invention.

Claims (6)

1. A method for preparing a supercapacitor electrode material by using a waste zinc-manganese battery is characterized in that the supercapacitor electrode material comprises a Zn-Mn blended oxide nano electrode material and a composite nano electrode material, and specifically comprises the following steps:
step 1, respectively recovering Zn and Mn elements from waste zinc-manganese batteries to obtain Mn (NO) 3 ) 2 Solution and ZnCl 2 A solution;
step 2, using Mn (NO) 3 ) 2 Solution and ZnCl 2 Respectively preparing a Zn-Mn blended oxide nano electrode material and a composite nano electrode material by using the solution:
1) Preparing a Zn-Mn blended oxide nano electrode material:
adding Mn (NO) 3 ) 2 Solution and ZnCl 2 Mixing the solution with 4:1-16 in a molar ratio, adding urea to adjust the pH value of the mixed solution to be neutral, adding ethanol into the mixed solution, wherein the volume of the ethanol and the volume of the mixed solution are 1.2-2, reacting at 100-180 ℃ for 12-24 h, fully washing a generated solid product with a deionized water and ethanol mixed solution with the volume ratio of 1 (0.3-3), filtering out precipitates, and drying to obtain the Zn-Mn blended oxide nano electrode material;
2) Preparing a composite nano electrode material: mixing charcoal powder according to a mass ratio of 1:0.5-3 to ZnCl 2 Fully soaking in the solution, filtering out precipitate, calcining for 2-6 hours at 700-1000 ℃ under inert atmosphere, fully washing with HCl with the concentration of 0.1-0.5mol/L to remove residual oxide in the biochar, washing with deionized water and drying to obtain activated biochar; then carrying out oxidation modification treatment on the activated charcoal to obtain surface oxidation modified charcoal; adding surface oxidation modified charcoal into Mn (NO) 3 ) 2 Mixing and fully soaking in the solution, adding organic solvent and ligand, ultrasonically pulverizing and emulsifying, thermally reacting at 120-200 deg.C for 12-24 h to obtain solid powder 2 Or calcining 2-8 h at 700-1000 ℃ under Ar atmosphere to obtain the composite nano electrode material.
2. The method for preparing the electrode material of the supercapacitor from the waste zinc-manganese batteries according to claim 1, wherein in the step 1, the specific steps of respectively recovering Zn and Mn from the waste zinc-manganese batteries are as follows: crushing the waste zinc-manganese dry batteries by adopting a mechanical crushing method, and respectively collecting a waste positive Mn compound and a waste negative Zn compound;
ultrasonically cleaning and filtering the Mn compound until the filtrate is neutral to obtain primary powder, and calcining the primary powder in a muffle furnace at 250-500 ℃ for 2-5 hours to obtain a recovered Mn compound; using 0.5-3 mol/L HNO 3 Solution with 30wt% H 2 O 2 Co-dissolvingCalcining the Mn compound, and filtering the filtrate to obtain recovered Mn (NO) 3 ) 2 A solution;
putting the Zn compound into 0.5-3 mol/L HCl solution, stirring until the Zn compound is dissolved, and obtaining the recovered ZnCl 2 And (3) solution.
3. The method for preparing the electrode material of the supercapacitor by using the waste zinc-manganese battery according to claim 1, wherein the preparation of the charcoal powder in the step 2 comprises the following specific steps: pulverizing peanut shells, corncobs, rice husks and wheat straws by a pulverizer, fully washing with deionized water to remove dust on the surface, drying in an oven, calcining at 400-550 ℃ in an inert atmosphere for 2-6 h, and fully grinding to obtain the charcoal powder.
4. The method for preparing the electrode material of the supercapacitor by using the waste zinc-manganese battery according to claim 1, wherein the step 2 of carrying out oxidation modification treatment on the activated charcoal comprises the following specific steps: mixing activated biochar with concentrated H 2 SO 4 Mixing with active biochar and concentrated H 2 SO 4 In a ratio of about 0.1g:10-50 mL, fully cooling at 0-5 ℃, and then adding KMnO 4 And NaNO 3 The mass ratio of the two is 1 (0.1-9), the reaction is carried out at the temperature of 40-80 ℃ for 0.5-5H, the mixture is diluted by deionized water after being cooled, and H is dripped dropwise 2 O 2 And standing until the mixture turns golden yellow or earthy yellow, and centrifugally washing and separating solid powder to obtain the biochar with the surface subjected to oxidation modification.
5. The method for preparing the electrode material of the supercapacitor by using the waste zinc-manganese dioxide battery according to claim 1, wherein the ligand in the step 2 is any one of terephthalic acid, trimesic acid, p-xylylenediamine, trimethylamine, 1-methylimidazole and benzimidazole.
6. The method for preparing the electrode material of the supercapacitor by using the waste zinc-manganese dioxide battery according to claim 1, wherein the organic solvent in the step 2 is one or a mixture of any two of methanol, ethanol, ethylene glycol, N-octanol and N, N-dimethylformamide.
CN201810556643.2A 2018-06-01 2018-06-01 Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery Active CN108808033B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810556643.2A CN108808033B (en) 2018-06-01 2018-06-01 Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810556643.2A CN108808033B (en) 2018-06-01 2018-06-01 Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery

Publications (2)

Publication Number Publication Date
CN108808033A true CN108808033A (en) 2018-11-13
CN108808033B CN108808033B (en) 2020-09-01

Family

ID=64090173

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810556643.2A Active CN108808033B (en) 2018-06-01 2018-06-01 Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery

Country Status (1)

Country Link
CN (1) CN108808033B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111048797A (en) * 2019-11-04 2020-04-21 石棉县东顺锌业有限责任公司 Method for producing zinc-containing nano material by using waste zinc-manganese battery
CN111710882A (en) * 2020-06-28 2020-09-25 金汤杰 Process for preparing lithium battery negative electrode material by using waste zinc-manganese battery
CN112259754A (en) * 2020-10-22 2021-01-22 上海交通大学 Method for recycling manganese from waste zinc-manganese dry battery positive electrode material and application
CN116495787A (en) * 2023-03-22 2023-07-28 四川大学 Manganese-based compound prepared based on waste lithium battery, preparation method of manganese-based compound and battery

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1530180A (en) * 2003-03-14 2004-09-22 于福东 Method for producing metal compound by waste zinc-manganese dioxide dry cell
CN101054187A (en) * 2007-04-03 2007-10-17 深圳市格林美高新技术股份有限公司 Selective volatilization recovery process and recovery system for waste zinc-manganese battery
CN101780952A (en) * 2010-03-26 2010-07-21 上海交通大学 Method for preparing loading functional oxide porous carbon
CN102136583A (en) * 2011-02-14 2011-07-27 华南师范大学 Regeneration method of zinc powder as negative electrode material of waste alkaline zinc-manganese dioxide battery
CN103151576A (en) * 2013-02-16 2013-06-12 东北大学 Method for preparing lithium battery cathode material by using waste zinc-manganese battery
CN104045116A (en) * 2014-06-12 2014-09-17 江苏大学 Preparation method of nano porous metal oxide/carbon lithium ion battery cathode material
CN106512944A (en) * 2016-12-06 2017-03-22 福建师范大学 Production method of oxidized wood active carbon for effectively adsorbing carbon dioxide

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1530180A (en) * 2003-03-14 2004-09-22 于福东 Method for producing metal compound by waste zinc-manganese dioxide dry cell
CN101054187A (en) * 2007-04-03 2007-10-17 深圳市格林美高新技术股份有限公司 Selective volatilization recovery process and recovery system for waste zinc-manganese battery
CN101780952A (en) * 2010-03-26 2010-07-21 上海交通大学 Method for preparing loading functional oxide porous carbon
CN102136583A (en) * 2011-02-14 2011-07-27 华南师范大学 Regeneration method of zinc powder as negative electrode material of waste alkaline zinc-manganese dioxide battery
CN103151576A (en) * 2013-02-16 2013-06-12 东北大学 Method for preparing lithium battery cathode material by using waste zinc-manganese battery
CN104045116A (en) * 2014-06-12 2014-09-17 江苏大学 Preparation method of nano porous metal oxide/carbon lithium ion battery cathode material
CN106512944A (en) * 2016-12-06 2017-03-22 福建师范大学 Production method of oxidized wood active carbon for effectively adsorbing carbon dioxide

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
宋永辉 兰新哲 何辉: "《提金氰化废水处理理论与方法》", 31 March 2015, 冶金工业出版社 *
许雪棠 等: "尖晶石型ZnMn204水热合成及光催化性能研究", 《无机盐工业》 *
长深根 刘波: "《重金属固废处理及资源化技术》", 31 December 2016, 冶金工业出版社 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111048797A (en) * 2019-11-04 2020-04-21 石棉县东顺锌业有限责任公司 Method for producing zinc-containing nano material by using waste zinc-manganese battery
CN111048797B (en) * 2019-11-04 2021-06-04 石棉县东顺锌业有限责任公司 Method for producing zinc-containing nano material by using waste zinc-manganese battery
CN111710882A (en) * 2020-06-28 2020-09-25 金汤杰 Process for preparing lithium battery negative electrode material by using waste zinc-manganese battery
CN112259754A (en) * 2020-10-22 2021-01-22 上海交通大学 Method for recycling manganese from waste zinc-manganese dry battery positive electrode material and application
CN116495787A (en) * 2023-03-22 2023-07-28 四川大学 Manganese-based compound prepared based on waste lithium battery, preparation method of manganese-based compound and battery

Also Published As

Publication number Publication date
CN108808033B (en) 2020-09-01

Similar Documents

Publication Publication Date Title
CN108808033B (en) Method for preparing electrode material of supercapacitor by using waste zinc-manganese battery
CN103896339B (en) A kind of preparation method of sodium manganese oxide
CN106299384B (en) Lithium-air battery positive electrode plate based on biochar
CN108172815B (en) Microspherical zinc vanadate, and preparation method and application thereof
CN101567442A (en) Method for preparing spinel lithium titanate
CN110690439B (en) P, N co-doped C/SiO prepared from silicon-containing biomassxGreen method for composite negative electrode material of lithium ion battery
CN104300124B (en) The preparation method of silicon/carbon dioxide compound and the application in lithium/sodium-ion battery
CN104466295A (en) Method for regenerating positive electrode active material in LiNi1/3Co1/3Mn1/3O2 waste lithium ion battery
CN108658119B (en) Method for preparing copper sulfide nanosheet and compound thereof by low-temperature vulcanization technology and application
CN103151576B (en) Method for preparing lithium battery cathode material by using waste zinc-manganese battery
CN105428612B (en) A kind of nanometer MoO2‑MoSe2@SFC lithium ion battery negative materials and preparation method thereof
CN107316987A (en) A kind of oxide nano thread/ZIF systems MOFs sugarcoated haws shape composites and preparation method thereof
CN103008653B (en) Carbon coated lead composite material and preparation method thereof
CN105958076A (en) Modified carbon material and preparation method thereof, cathode lead paste, polar plate and lead carbon battery
CN107134372A (en) Ultracapacitor based on transient metal sulfide/nitrogen-doped graphene Yu di-iron trioxide/graphene
CN102386383B (en) Lithium battery hard carbon microsphere cathode material with core-shell structure and preparation method thereof
CN105932278B (en) A kind of nanometer sheet self assembly prism-frustum-shaped (NH4)2V3O8Preparation method
CN107337205A (en) One is changed into the method for sodium ion battery electrode material using discarded maize straw
CN104300133A (en) Carbon nanotube coated lithium titanate material and its preparation method
CN111036651A (en) Recovery system of positive electrode waste slurry of lithium battery
CN108376789A (en) Method for recycling waste alkaline manganese batteries into primary zinc-air batteries
CN103276406B (en) Electrochemical lithium recovery method
CN114665053A (en) Manganese dioxide nano-material positive pole piece, preparation method thereof and zinc ion battery containing manganese dioxide nano-material positive pole piece
Zhang et al. Regeneration of high-performance materials for electrochemical energy storage from assorted solid waste: A review
CN114318368A (en) Special electrolytic manganese dioxide for lithium manganate battery and preparation method and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant