technical field
[One]
The present invention relates to a method of recycling resources when manufacturing a lithium secondary battery. The present invention particularly relates to a method of recovering and reusing positive electrode scrap generated in a lithium secondary battery manufacturing process or a positive electrode active material of a lithium secondary battery that is discarded after use. This application is a priority claim application for Korean Patent Application No. 10-2020-0062370 filed on May 25, 2020, and all contents disclosed in the specification and drawings of the application are incorporated herein by reference.
background
[2]
Lithium secondary batteries that can be repeatedly charged and discharged are in the spotlight as an alternative to fossil energy. Lithium secondary batteries have been mainly used in traditional hand-held devices such as cell phones, video cameras, and power tools. However, in recent years, electric vehicles (EVs, HEVs, PHEVs), large-capacity power storage devices (ESSs), uninterruptible power supply systems (UPS), etc., the application fields are gradually increasing.
[3]
A lithium secondary battery includes an electrode assembly in which unit cells having a structure in which a positive electrode plate and a negative electrode plate coated with an active material are coated on a current collector with a separator interposed therebetween, and a casing for sealing and housing the electrode assembly together with an electrolyte, that is, a battery case to provide The cathode active material of the lithium secondary battery mainly uses a lithium-based oxide, and the anode active material uses a carbon material. The lithium-based oxide contains a metal such as cobalt, nickel, or manganese. In particular, cobalt, nickel, and manganese are very expensive valuable metals. Among them, cobalt is a strategic metal, and each country in the world has a special interest in supply and demand. is known If there is an imbalance in the supply and demand of raw materials for strategic metals, raw material prices are highly likely to rise.
[4]
In the past, research on recovering and recycling these valuable metals from lithium secondary batteries (waste batteries) that are discarded after their lifespan has been completed has been mainly conducted. In addition to the waste battery, it is more preferable if resources can be recovered from the waste discarded after the positive electrode plate is punched or from the positive electrode having a defect in the process.
[5]
Currently, in the manufacture of lithium secondary batteries, as shown in FIG. 1 , a cathode active material layer 20 is coated with a cathode active material, a conductive material, a binder, a solvent, etc. ) by forming the positive electrode sheet 30, and then punching out the positive electrode plate 40 to a certain size. The part remaining after punching is discarded as anode scrap (scrap, 50). If it is possible to recover the positive active material from the positive electrode scrap 50 and reuse it, it would be very desirable from an industrial-economic point of view and an environmental point of view.
[6]
Conventionally, the method of recovering the positive active material is mostly used as a raw material for the synthesis of the positive active material by dissolving the positive electrode in hydrochloric acid, sulfuric acid, nitric acid, etc., extracting active material elements such as cobalt, nickel, and manganese. However, the method of extracting active material elements using acid has disadvantages in that the process for recovering the pure raw material is not environmentally friendly and requires a neutralization process and a wastewater treatment process, which increases the process cost. In addition, lithium, which is one of the main elements of the cathode active material, cannot be recovered. In order to solve this disadvantage, a method that can be directly reused without dissolving the cathode active material and extracting the active material in elemental form is required.
DETAILED DESCRIPTION OF THE INVENTION
technical challenge
[7]
The problem to be solved by the present invention is to provide a method for recovering and reusing an active material from a cathode scrap.
means of solving the problem
[8]
In order to solve the above problems, the cathode active material reuse method of the present invention comprises (a) heat-treating a cathode scrap including a lithium cobalt oxide cathode active material layer on a current collector in air to thermally decompose a binder and a conductive material in the active material layer, separating the current collector from the active material layer and recovering the active material in the active material layer; (b) washing the recovered active material with an aqueous lithium compound solution showing basicity in an aqueous solution and drying; and (c) adding a lithium precursor to the washed active material and annealing to obtain a reusable active material.
[9]
The heat treatment may be performed at 300 to 650 °C.
[10]
The heat treatment may be performed at 550° C. for 30 minutes at a temperature increase rate of 5° C./min.
[11]
The washing may be performed by stirring the recovered active material simultaneously with the impregnation of the lithium compound aqueous solution.
[12]
The lithium compound aqueous solution is prepared to contain more than 0% and 15% or less of the lithium compound, and preferably LiOH is used. The washing may be performed within 1 hour.
[13]
The lithium precursor may be any one or more of LiOH, Li 2CO 3 , LiNO 3 and Li 2O.
[14]
The lithium precursor may be added in an amount capable of adding as much as the ratio of lithium lost compared to the ratio of lithium and other metals in the raw material active material used for the active material layer.
[15]
For example, the lithium precursor may be added in an amount in which lithium is added in a molar ratio of 0.001 to 0.4.
[16]
The annealing may be performed at 400 to 1000° C. in air.
[17]
The temperature of the annealing step may be a temperature exceeding the melting point of the lithium precursor.
[18]
The active material in the active material layer is recovered in the form of a powder, and carbon components generated by carbonization of the binder or the conductive material may not remain on the surface.
[19]
The reusable active material may have a particle size distribution similar to that of the active material in the active material layer.
[20]
Another positive electrode active material reuse method according to the present invention is (a) a positive electrode including a lithium cobalt oxide positive electrode active material layer on a current collector, a positive electrode scrap remaining after punching out a positive electrode scrap in the air at 300 ~ 650 ℃ heat treatment to the active material separating the current collector from the active material layer and recovering the active material in the active material layer by thermally decomposing the binder and the conductive material in the layer; (b) washing and drying the recovered active material with an aqueous lithium compound solution containing more than 0% and not more than 15% lithium compound, showing basicity in an aqueous solution; and (c) adding at least one of LiOH, Li 2CO 3, LiNO 3 and Li 2O to the washed active material and annealing in air at 400 to 1000° C.
Effects of the Invention
[21]
According to the present invention, the waste positive electrode active material such as positive electrode scrap generated during the manufacturing process of a lithium secondary battery can be reused without using an acid, so it is eco-friendly. The method according to the present invention does not require a neutralization process or a wastewater treatment process, so it is possible to alleviate environmental issues and reduce process costs.
[22]
According to the present invention, the positive electrode active material can be recovered without the unrecoverable metal element. Since the current collector is not dissolved, the current collector can also be recovered. It is economical because it is a method that can directly reuse the active material recovered in powder form, rather than extracting the active material element and using it again as a raw material for synthesizing the cathode active material.
[23]
According to the present invention, it is safe because it does not use toxic and explosive solvents such as NMP, DMC, acetone, and methanol, and because simple processes such as heat treatment, washing, and annealing are used, process management is easy and suitable for mass production.
Brief description of the drawing
[24]
The following drawings attached to the present specification illustrate embodiments of the present invention, and together with the detailed description to be described later serve to further understand the technical spirit of the present invention, the present invention is limited only to the matters described in those drawings should not be interpreted as
[25]
1 is a view showing positive electrode scrap discarded after the positive electrode plate is punched from the positive electrode sheet.
[26]
2 is a flowchart of an active material reuse method according to the present invention.
[27]
3 is a result of cell evaluation using the active materials of Examples and Comparative Examples.
[28]
4 is an X-ray diffraction (XRD) pattern of the active materials of Examples and Comparative Examples.
[29]
5 is a scanning electron microscope (SEM) photograph of the active materials of Examples and Comparative Examples.
[30]
6 is a particle size distribution graph of the active materials of Examples and Comparative Examples.
Modes for carrying out the invention
[31]
Hereinafter, embodiments of the present invention will be described with reference to the accompanying drawings. Prior to this, the terms or words used in the present specification and claims should not be construed as being limited to their ordinary or dictionary meanings, and the inventor should properly understand the concept of the term in order to best describe his or her application. Based on the principle that it can be defined, it should be interpreted as meaning and concept consistent with the technical idea of ​​the present invention. Accordingly, since the embodiments described in this specification and the configurations shown in the drawings are only one embodiment of the present invention and do not represent all the technical spirit of the present invention, various equivalents that can be substituted for them at the time of the present invention It should be understood that there may be variations and variations.
[32]
DETAILED DESCRIPTION In the following description, reference is made to the accompanying drawings, which form a part hereof. The implementations, drawings, and claims described in the detailed description are not intended to be limiting. Other embodiments may be utilized and other changes may be made without departing from the spirit and scope of the subject matter disclosed herein. It is immediately understood that aspects of the invention, as generally described herein and illustrated in the drawings, can be arranged, substituted, combined, separated, and designed in various other configurations, all of which are expressly contemplated herein. will be able
[33]
Unless defined otherwise, all technical and scientific terms used herein generally have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
[34]
The invention is not limited with respect to the specific embodiments described herein. As will be apparent to those skilled in the art, many changes and modifications can be made without departing from the spirit and scope of the present invention. In addition to those enumerated herein,Functionally equivalent methods will be apparent to those skilled in the art from the foregoing descriptions. Such changes and modifications are intended to fall within the scope of the appended claims. The invention shall be limited only by the claims, along with the full scope of equivalents to which such claims are entitled. It should be understood that the invention is not limited to particular methods, which may, of course, vary. It is also to be understood that the terminology used herein is used for the purpose of describing particular embodiments only, and is not intended to be limiting.
[35]
In the case of the conventional active material recycling process, if the main purpose was to extract valuable metals (nickel, cobalt, manganese, etc.) as elements in the lithium secondary battery active material whose performance has deteriorated after use and to resynthesize the active material, the present invention is a lithium secondary battery There is a difference in that the active material is also recovered from the cathode scrap generated during the manufacturing process.
[36]
In addition, in the case of the known active material recycling process, there is a chemical method such as extracting a valuable metal through acid/base dissolution or melting using reduction/additive, and manufacturing it as a metal (direct reduction method) or a resynthesized active material. In addition, the complexity and economic cost of the process are additionally added. However, the present invention relates to a method of directly reusing a cathode active material without dissolving it.
[37]
In order to directly reuse the positive electrode active material, a method for removing the current collector from the positive electrode is required. To remove the current collector from the positive electrode, it is possible to remove the binder through high-temperature heat treatment, to melt the binder using a solvent, to completely melt the current collector, and to select the active material through dry grinding and sieving. do.
[38]
The stability of the solvent is important in dissolving the binder using the solvent. NMP is probably the most efficient solvent, but it has the disadvantages of toxicity and high price. In addition, there is a disadvantage that a solvent recovery process such as reprocessing the waste solvent is required. Melting the current collector will be cheaper than using a solvent. However, there is a risk of explosion because it is difficult to remove foreign substances from the surface of the reusable active material and hydrogen gas is generated during the current collector removal process. It is difficult to completely separate the current collector and the active material by dry grinding and sieving. During the pulverization process, the particle size distribution of the active material is changed, and since it is difficult to remove the binder, there is a disadvantage in that the characteristics of the reused battery deteriorate.
[39]
In the present invention, the active material and the current collector are separated using high-temperature heat treatment. In particular, since heat treatment is carried out in air, it is advantageous for mass production and commercialization because it is a relatively simple process that does not require a special device configuration and only needs to be heated. However, foreign substances should not remain on the surface of the reusable active material. In the present invention, even the step of removing foreign substances from the surface of the reusable active material is proposed.
[40]
Hereinafter, an active material reuse method according to an embodiment of the present invention will be described with reference to FIG. 2 . 2 is a flowchart of an active material reuse method according to the present invention.
[41]
Referring to FIG. 2 , first, a cathode scrap to be discarded is prepared (step s10).
[42]
As described above with reference to FIG. 1 , the positive electrode scrap may be a portion remaining after manufacturing a positive electrode sheet including a positive electrode active material layer on a current collector and punching out. In addition, it is possible to prepare anode scrap by collecting anodes having defects during the process. In addition, positive electrode scrap may be prepared by separating the positive electrode from the discarded lithium secondary battery after use.
[43]
For example, NMP (N-methyl pyrrolidone) is added and mixed to an active material such as LiCoO 2 (LCO), which is lithium cobalt oxide, carbon black as a conductive material, and polyvinylidene fluoride (PVdF) as a binder. The prepared slurry is coated on a sheet-type current collector made of aluminum foil, dried in a vacuum oven at about 120° C. to prepare a positive electrode sheet, and then a positive electrode plate of a certain size is punched out and the remaining positive electrode scrap is prepared. .
[44]
As described above, the positive electrode scrap has an active material layer on a current collector of a metal foil such as aluminum foil. The active material layer is formed by coating a slurry in which an active material, a conductive material, a binder, a solvent, etc. are mixed, and has a structure in which the binder connects the active material and the conductive material after the solvent is volatilized. Therefore, if the binder is removed, the active material may be separated from the current collector.
[45]
Next, the anode scrap is crushed to an appropriate size (step s20). Shredding refers to the cutting or shredding of anode scrap into pieces of suitable, easy-to-handle size. After crushing, the anode scrap is cut into small pieces, for example 1 cm x 1 cm. For crushing, various dry crushing equipment such as hand-mill, pin-mill, disk-mill, cutting-mill and hammer-mill may be used, or a high-speed cutter may be used.
[46]
Crushing can be carried out in consideration of the characteristics required in the equipment used in the handling and subsequent processes of the anode scrap. For example, in the case of using equipment that requires continuous processing in loading and unloading anode scrap, the fluidity of the anode scrap must be good, so that too large anode scrap must be crushed.
[47]
Now, the anode scrap is heat-treated in air (step s30).
[48]
In the present invention, the heat treatment is performed to thermally decompose the binder in the active material layer. Heat treatment can be carried out at 300 ~ 650 ℃ can also be called high temperature heat treatment. At a temperature of less than 300 ℃, it is difficult to remove the binder, so there is a problem that the current collector cannot be separated. At a temperature of 650 ℃ or more, the current collector melts (Al melting point: 660 ℃), and the current collector cannot be separated.
[49]
The heat treatment time is maintained so that the binder can be sufficiently thermally decomposed. For example, around 30 minutes. Preferably it is set as 30 minutes or more. The longer the heat treatment time, the longer the time for thermal decomposition of the binder to occur. Preferably, the heat treatment time is 30 minutes or more and less than 5 hours.
[50]
The heat treatment equipment may be various types of furnaces. For example, it may be a box-type furnace or a rotary kiln capable of continuous processing in consideration of productivity.
[51]
After heat treatment, it may be slowly cooled or rapidly cooled in the atmosphere.
[52]
For example, the heat treatment may be performed at 550° C. for 30 minutes at a temperature increase rate of 5° C./min. The temperature increase rate is, for example, a degree that can be implemented without excessive force in a box-type furnace and can be heated without generating a thermal shock or the like to the anode scrap. 550°C is to allow the thermal decomposition of the binder to occur well while considering the melting point of the Al current collector. At this temperature, heat treatment for less than 10 minutes is insufficient for thermal decomposition, so heat treatment should be carried out for more than 10 minutes, and heat treatment should be performed for more than 30 minutes if possible.
[53]
As the binder and conductive material in the active material layer are thermally decomposed through heat treatment in air, they become CO 2 and H 2O and are removed. Since the binder is removed, the active material is separated from the current collector, and the active material to be recovered may be selected in powder form. Accordingly, only in step s30, the current collector may be separated from the active material layer and the active material in the active material layer may be recovered.
[54]
It is important that the heat treatment of step s30 be performed in air. If the heat treatment is performed in a reducing gas or inert gas atmosphere, the binder and the conductive material are not thermally decomposed and only carbonized. When carbonization is done, the carbon component remains on the surface of the active material, thereby degrading the performance of the reusable active material. When heat treatment is performed in air, the carbon material in the binder or the conductive material reacts with oxygen and is burned and removed as CO and CO 2 gas, so that almost all of the binder and the conductive material are removed without remaining.
[55]
Therefore, according to the present invention, the active material is recovered in the form of a powder, and the carbon component generated by carbonization of the binder or the conductive material may not remain on the surface.
[56]
Next, the recovered active material is washed and dried (step s40). When washing, it is important to wash with an aqueous solution of a lithium compound showing basicity in an aqueous solution. This lithium compound aqueous solution is prepared to contain more than 0% and not more than 15% of the lithium compound, and preferably LiOH is used. The amount of LiOH is preferably 15% or less. The use of excess LiOH may leave excess LiOH on the surface of the active material even after washing, which may affect future annealing processes. In order to clean the surface of the active material in the pre-annealing step as much as possible, the addition of excess LiOH is not good for the process, so it is limited to 15% or less.
[57]
Washing can be performed by immersing the recovered active material in such an aqueous lithium compound solution. After immersion, washing may be performed within a week, preferably within one day, and still more preferably within one hour. When washing for more than a week, there is a risk of capacity degradation due to excessive lithium elution. Therefore, it is preferable to carry out within 1 hour. Washing includes immersing the active material in an aqueous lithium compound solution showing basicity in an aqueous solution state, stirring the immersion state, and the like. It is best to combine agitation as much as possible. If the lithium compound is immersed in an aqueous solution without stirring, the washing process is slow and may cause lithium leaching. Since the process time can be minimized if the stirring is performed in parallel, it is preferable that the stirring be performed simultaneously with the impregnation of the lithium compound aqueous solution. Drying may be performed in air in an oven (convection type) after filtration.
[58]
The reason for washing with an aqueous solution of a lithium compound showing basicity in an aqueous solution is to remove LiF and metal fluoride, which may be present on the surface of the recovered active material, and to perform surface modification. During the heat treatment of step s30, the binder and the conductive material in the active material layer are vaporized and removed as they become CO 2 and H 2 O. In this process, CO 2 and H 2 O react with lithium on the surface of the active material to form Li 2CO 3 and LiOH, and PVdF F, which was present in the same binder, reacts with the metal element constituting the positive electrode active material to form LiF or metal fire.Cargo may also be formed. If LiF or metal fluoride remains, battery characteristics deteriorate when the active material is reused. In the present invention, by adding a washing step as in step s40 to remove reactants that may have been generated on the surface of the reused active material during the heat treatment step (s30), foreign substances are not left on the surface of the recycled active material.
[59]
In step s40, it is important to wash with an aqueous solution of a lithium compound showing basicity in an aqueous solution. If an aqueous solution of sulfuric acid or hydrochloric acid is used rather than an aqueous solution of a lithium compound showing basicity in an aqueous solution, it is possible to wash F on the surface of the active material. make it The lithium compound aqueous solution showing basicity in the aqueous solution state used in the present invention can not only remove the binder that may remain in a trace amount even after the thermal decomposition of step s30, but also does not elute the transition metal, etc. present in the active material, and in the washing process It is very preferable because it can also serve to supplement the amount of lithium that can be eluted.
[60]
Next, a lithium precursor is added to the washed active material and annealed (step s50). Through step s50, a reusable active material may be obtained.
[61]
Loss of lithium in the active material may occur during the preceding steps s30 and s40. In step s50, such lithium loss is compensated.
[62]
In addition, in step s50, the crystal structure of the active material is restored through annealing to restore or improve the properties of the reused active material to the level of a fresh active material that has never been used.
[63]
During the previous steps s30 and s40, a deformed structure may appear on the surface of the active material. In addition, in the case of the LCO active material, Co 3 O 4 may be generated by thermal decomposition on the surface. If the battery is manufactured while Co 3 O 4 is present as it is, battery characteristics may deteriorate. In the present invention, the initial properties can be restored or improved to a level similar to that of the fresh active material by restoring the crystal structure and removing Co 3 O 4 through step s50.
[64]
The lithium precursor in step s50 may be any one or more of LiOH, Li 2CO 3 , LiNO 3 and Li 2O.
[65]
The lithium precursor is added in an amount capable of adding as much as the ratio of lithium lost compared to the ratio of lithium and other metals in the raw material active material (ie, fresh active material) used in the active material layer. For example, when the ratio of lithium to other metals in the fresh active material is 1, a lithium precursor in an amount capable of adding lithium in a molar ratio of 0.001 to 0.4 may be added. Preferably, lithium in a molar ratio of 0.01 to 0.2 is added. Addition of an excess lithium precursor other than the amount of lithium lost through washing, etc. leaves unreacted lithium precursors in the reused active material, which serves to increase resistance in the active material reuse process, so that it is necessary to administer an appropriate amount of the lithium precursor.
[66]
Annealing may be performed at 400 to 1000° C. in air. The annealing temperature may be 600-900°C. This temperature should be changed within a limited range depending on the type of the lithium precursor. It is preferable to set the annealing time to 1 hour or more. Preferably, it is about 5 hours. If the annealing time is long, the crystal structure can be sufficiently recovered, but even if it is used for a long time, the performance is not significantly affected. Annealing time is made into 15 hours or less, for example. The annealing equipment may use the same or similar equipment as in the heat treatment step s30.
[67]
For example, when Li 2CO 3 is used as a lithium precursor, the annealing temperature is preferably 700 to 900°C, more preferably 710 to 780°C. This is because the melting point of Li 2CO 3 is 723°C. Most preferably, it is carried out at 750°C. In the case of using LiOH as a lithium precursor, the annealing temperature is preferably 400 to 600°C, more preferably 450 to 480°C. This is because the melting point of LiOH is 462°C.
[68]
The annealing temperature is preferably a temperature exceeding the melting point of the lithium precursor. However, at a temperature exceeding 1000°C, thermal decomposition of the positive electrode active material occurs and the performance of the active material is deteriorated, so that the temperature should not exceed 1000°C.
[69]
As described above, according to the present invention, LiF or metal fluoride is removed in step s40 of washing, Co 3O 4 is removed in step s50 of annealing. The washing and drying steps using an aqueous lithium compound solution showing basicity in an aqueous solution are safe and inexpensive, and can remove LiF or metal fluoride without loss of other elements, prevent elution of transition metals, etc. It has the advantage of compensating for lithium losses. Although the annealing step is also safe and inexpensive, Co 3 O 4 can be effectively removed, and the cell characteristics of the reused active material can be recovered by improving crystal structure recovery, that is, crystallinity.
[70]
The reusable active material obtained according to the present invention may have a particle size distribution similar to that of the active material existing in the active material layer in the positive electrode scrap, and thus may not require a separate treatment. Since the carbon component generated by the binder or the conductive material does not remain on the surface, a step or the like for removing the carbon component is not required. Accordingly, the active material obtained through the method of FIG. 2 may be reused as it is without additional treatment and used to manufacture the positive electrode.
[71]
100% of the reusable active material can be used as it is without adjusting the composition, or it can be mixed with fresh LCO and mixed with a conductive material, a binder, and a solvent to form a slurry.
[72]
Hereinafter, an experimental example of the present invention will be described in detail.
[73]

[74]
Each positive electrode active material was prepared in the same manner as in Examples and Comparative Examples below, and electrochemical performance was evaluated.
[75]
Example: A reused active material was collected according to the method for reusing an active material of the present invention as described above. After the positive electrode plate was punched, the positive electrode scrap was prepared and the heat treatment in step s30 was performed at 550° C. for 30 minutes. The washing of step s40 was performed for 10 minutes using LiOH. In step s50, a lithium precursor (Li 2CO 3) in an excess of 2 mol% lithium relative to the lithium amount in the reused LCO was added and annealed at 750° C. for 15 hours.
[76]
Comparative Example 1: Fresh LCO was used instead of a reused active material.
[77]
Comparative Example 2: Only the heat treatment of step s30 of the active material reuse method of the present invention as described above was performed to remove the binder, the conductive material, and the Al current collector, and the LCO active material was collected. Step s30 was performed under the same conditions as in Example. In the active material reuse method of the present invention, the surface modification of step s40 and the crystal structure recovery of step s50 were not performed.
[78]
Comparative Example 3: Further in Comparative Example 2, the surface modification of step s40 of the active material reuse method of the present invention as described above was performed to collect the LCO active material. That is, the surface modification was performed, but the crystal structure recovery of step s50 in the active material reuse method of the present invention was not performed. Step s40 was performed under the same conditions as in Example.
[79]
96 wt% of the positive active material recovered or prepared in each of the Examples and Comparative Examples, 2 wt% of carbon black, a conductive material, and 2 wt% of PVdF, a binder, mixed with NMP to make a slurry to prepare a positive electrode Half Cell, CHC) was prepared and the electrochemical performance was evaluated.
[80]
3 is a result of cell evaluation using the active materials of Examples and Comparative Examples. At different currents, the rate performance was examined by evaluating the capacity according to the number of cycle repetitions. The equipment used for evaluation is a general charging/discharging test device that is well used in the laboratory. There is no deviation depending on the measuring device or method. In the graph of FIG. 3 , the horizontal axis indicates the number of cycles and the vertical axis indicates capacity.
[81]
The voltage was set to 3-4.5V, and the initial formation charge/discharge was performed at 0.2C/0.2C. The electrolyte constituting the cell was carbonate-based, with Ethylene carbonate(EC):Ethyl methyl carbonate(EMC)=3:7 and some additives were used.
[82]
Referring to FIG. 3 , although it is a reusable active material, it can be seen that the lowest rate performance is obtained in Comparative Example 2 in which the surface modification and crystal structure recovery according to the present invention are not performed. In the high-temperature heat treatment process such as step s30, as the binder and conductive material are removed as CO 2 and H 2 O, it reacts with lithium on the surface of the positive electrode active material to form Li 2CO 3 and LiOH, and reacts with F present in the binder to form LiF or metal fluoride. because it was formed. In addition, it is judged to show low battery characteristics due to Co 3 O 4 generated by thermal decomposition on the LCO surface.
[83]
Comparative Example 3 was a surface modification compared to Comparative Example 2. Comparative Example 3 is evaluated to be able to obtain better results than Comparative Example 2 because the reactants generated on the surface were removed through washing.
[84]
In Example 3, compared to Comparative Example 3, annealing was performed. In order to supplement lithium lost in the process of recovering the active material and recover crystallinity, Li 2CO 3 was added and annealed. Not only can the insufficient amount of lithium generated during the process be compensated, but the deformed structure and Co 3O 4 that may appear on the surface of the active material during regeneration are reduced back to the LCO crystal structure, resulting in improved results compared to the initial properties of the fresh active material of Comparative Example 1. is confirmed to show As described above, according to the present invention, the active material can be recovered from the cathode scrap to a level that can be directly reused. It is safe because it does not use toxic and explosive solvents such as NMP, DMC, acetone, and methanol, and it is suitable for mass production because it uses simple and safe methods such as heat treatment, washing and drying, and annealing.
[85]
4 is an XRD pattern of the active materials of Examples and Comparative Examples.In the XRD pattern, the horizontal axis is 2θ (Theta) (degrees), and the vertical axis is intensity. The XRD pattern was obtained using a general X-ray diffraction apparatus that is well used in the laboratory. For example, it can be analyzed using an X-ray diffractometer XG-2100 manufactured by Rigaku. However, there is no deviation depending on the device or method.
[86]
4A is an XRD pattern of Comparative Example 1, that is, fresh LCO. (b) is the XRD pattern of the active material of Comparative Example 2, and (c) is the XRD pattern of the active material of Comparative Example 3. Comparing (b) and (c) with (a), the Co 3 O 4 phase is confirmed. That is, it can be confirmed that Co 3 O 4 is generated on the surface of the LCO in the heat treatment process of step s30.
[87]
Figure 4 (d) is an XRD pattern of the active material of Example. Comparing (c) and (d), it can be seen that the Co 3 O 4 phase is lost through the annealing of step s50 and the crystal structure is restored to LCO. Looking at the position of the diffraction peak in the XRD pattern, the crystal structure of (d) is similar to the crystal structure of (a). Therefore, it can be confirmed that the Example of the present invention is restored to the level of the fresh active material of Comparative Example 1. As described above, according to the present invention, the active material can be recovered from the cathode scrap to a level that can be directly reused.
[88]
5 is an SEM photograph of the active materials of Examples and Comparative Examples. The SEM pictures were taken with a general SEM device that is well used in the laboratory. did. For example, you can take pictures using HITACHI's s-4200. However, there is no deviation depending on the measuring device or method.
[89]
Figure 5 (a) is a SEM photograph of the fresh LCO of Comparative Example 1, (b) is a SEM photograph of the reused active material of Example. It can be seen that the recovered LCO of the example also exhibits the same shape when compared with the fresh LCO. In addition, since only LCO is observed, it is confirmed that the binder and the conductive material are removed during the high-temperature heat treatment process. Therefore, it can be seen that the active material is separated from the current collector only by heat treatment in air, and almost no binder or conductive material remains on the surface of the active material. As described above, according to the present invention, it is possible to separate the current collector and the active material without using a complicated method or harmful substances, so that the active material can be recovered in an environmentally friendly manner. Since it can be reused without the use of acid, it does not require a neutralization process or wastewater treatment process, thereby alleviating environmental issues and reducing process costs.
[90]
6 is a particle size distribution graph of the active materials of Examples and Comparative Examples. The particle size distribution can be obtained with a general particle size analyzer well used in the laboratory. For example, it can be specified using a Horiba LA 950V2 particle size analyzer. However, there is no deviation depending on the measuring device or method. In FIG. 6 , the horizontal axis represents particle size (um) and the vertical axis represents volume %.
[91]
All of the active materials recovered in Examples and Comparative Examples 2 and 3 have similar particle size distributions compared to the fresh LCO of Comparative Example 1. It is defined that the particle size distribution is similar when the volume % of particles having the same particle size differs only within +/- 2%. As described above, according to the present invention, since the particle size distribution of the active material does not change, the initial characteristics are almost maintained, and it can be expected that the characteristics of a battery using the reused battery characteristics will be similar to those of a battery using a fresh active material.
[92]
As described above, according to the present invention, the cathode scrap can be reused using a simple, eco-friendly, and economical method, and even if a lithium secondary battery is manufactured by reusing the LCO cathode active material prepared in this way, there is no problem in the performance of the battery. .
[93]
Although the present invention has been described above with reference to limited embodiments and drawings, the present invention is not limited thereto, and various modifications and variations can be made by those skilled in the art within the scope of the technical spirit of the present invention and the claims to be described below. Of course it is possible.

Claims

[Claim 1]
(a) by thermally decomposing the binder and the conductive material in the active material layer by thermally decomposing the positive electrode scrap including the lithium cobalt oxide positive electrode active material layer on the current collector in air, the current collector is separated from the active material layer and the active material in the active material layer recovering; (b) washing the recovered active material with an aqueous lithium compound solution showing basicity in an aqueous solution and drying; and (c) adding a lithium precursor to the washed active material and annealing to obtain a reusable active material.
[Claim 2]
The method of claim 1, wherein the heat treatment is performed at 300 to 650°C.
[Claim 3]
The method of claim 1 , wherein the lithium compound aqueous solution is prepared to contain more than 0% and 15% or less of the lithium compound, and the washing is performed within 1 hour.
[Claim 4]
The method of claim 1 , wherein the washing is performed by stirring the recovered active material simultaneously with the impregnation of the lithium compound aqueous solution.
[Claim 5]
The method of claim 1 , wherein the lithium precursor is at least one of LiOH, Li 2CO 3 , LiNO 3 and Li 2O.
[Claim 6]
The method of claim 1 , wherein the amount of lithium that is lost compared to the ratio of lithium and other metals in the raw material active material used in the active material layer is added in an amount that can be added.
[Claim 7]
The method of claim 6 , wherein the lithium precursor is added in an amount to which lithium is added in a molar ratio of 0.001 to 0.4.
[Claim 8]
The method of claim 1 , wherein the annealing is performed at 400 to 1000° C. in air.
[Claim 9]
The method of claim 1 , wherein the temperature of the annealing step exceeds the melting point of the lithium precursor.
[Claim 10]
The method of claim 1 , wherein the active material in the active material layer is recovered in a powder form, and a carbon component generated by carbonization of the binder or the conductive material does not remain on the surface.
[Claim 11]
The method of claim 1 , wherein the reusable active material has a particle size distribution similar to that of the active material in the active material layer.
[Claim 12]
(a) by thermally decomposing the binder and the conductive material in the active material layer by thermally decomposing the positive electrode scrap, which is the portion remaining after the positive electrode plate is punched out from the positive electrode including the lithium cobalt oxide positive electrode active material layer on the current collector, at 300 to 650° C. in air, separating the current collector from the active material layer and recovering the active material in the active material layer; (b) washing and drying the recovered active material with an aqueous lithium compound solution containing more than 0% and not more than 15% lithium compound, showing basicity in an aqueous solution; and (c) adding at least one of LiOH, Li 2CO 3, LiNO 3 and Li 2O to the washed active material and annealing in air at 400 to 1000° C.