Krystal
Davis
*ab and
George P.
Demopoulos
*a
aMining and Materials Engineering, McGill University, 3610 University Street, Montreal, QC H3A 0C5, Canada. E-mail: George.demopoulos@mcgill.ca
bEnergy, Mining and Environment, National Research Council of Canada, 1200 Montreal Rd., Ottawa, ON K1A 0R6, Canada. E-mail: Krystal.Davis@nrc-cnrc.gc.ca
First published on 16th October 2023
The supply chain for raw materials needed to fulfill the demand for lithium-ion battery (LIB) manufacturing is less than certain. With the stress and uncertainty of securing the raw materials, predicted price increases in metals such as lithium and nickel could jeopardize the economics in EV battery production. Lithium-ion battery recycling could help alleviate the demands on critical virgin materials. This would realize a price parity goal, $100 per kW h, for internal combustion engines (ICE) and EVs. Simultaneously, recycling could reduce waste in landfill sites as 1 M tonnes of LIBs are set to retire by 2030. In this context the recycling of LIBs becomes imperative, but this industrial activity must be done in full compliance with sustainability principles. For example, current industrial recycling technologies tend to generate a lot of waste products as only some value metals are recovered while simultaneously tend to be energy intensive with heavy chemical usage and risks of water and soil contamination. In this review we focus on spent nickel-manganese-cobalt (NMC) lithium-ion batteries that currently dominate the EV market examining primarily their recycling by hydrometallurgical processing as this route seems to be the most advocated. Our review compares the different hydrometallurgical process flowsheets seeking to highlight areas for chemical and technological improvement as they are proposed in recent patented R&D developments. The review concludes with the strong endorsement of hydrometallurgy-based direct recycling approach as the most sustainable route.
Sustainability spotlightNi–Mn–Co oxides (NMC) are currently the preferred cathode materials in Li-ion batteries (LIB) powering the electric vehicle (EV) revolution. The composition chemistry of these cathodes constantly evolves while at the same time the volume of spent batteries exponentially increases demanding new advanced sustainable recycling technologies. Currently the industrial NMC recycling practice targets mainly the recovery of the valuable metals by pyrometallurgical and hydrometallurgical processes, or a combination of both. However, these have several limitations, including high energy and/or chemical consumption, incomplete recovery of metals, and GHG emissions. To overcome these limitations, there are new R&D developments in hydrometallurgical recycling technologies. One area of development is the use of novel solvents to improve metal recovery rates. Another exciting development is a paradigm-shift towards direct recycling of the active cathode material (CAM) enabled by innovative hydrometallurgical treatment that avoids breaking it down into its constituent elements. Direct recycling may be combined with upcycling, thereby further promoting circularity and less dependency on raw material extraction. Our review relates to the following UN SDGs: affordable and clean energy (SDG 7), industry & innovation (SDG 9), responsible consumption and production (SDG 12), and climate action (SDG 13). |
Battery chemistries have evolved over the years, two factors have driven research and innovation; increasing density, thus battery life and range, and reducing material costs.5 The most common battery chemistry in EV LIB cathodes are lithium, nickel, manganese and cobalt oxide (NMC) batteries. The cathode can be any mixture of LiNixMnyCozO2, NMC (where x, y and z = 1). Other chemistries such as lithium iron phosphate (LFP), LiNixCoyAlzO2, NCA (where x, y and z = 1), lithium manganese oxide (LMO) and lithium cobalt oxide (NCO), are commercially available but for this study we will look at the NMC battery only.6 The NMC cathode has become economically more desirable, the cobalt content has decreased (NMC 111, NMC 523, NMC 622, NMC 811) improving not only overall cost but also lessening the environmental and ethical impacts. The density has also improved with the increase in nickel content, NMC 811, improving the range.7
Some of the LIB raw material have been listed as critical in countries like Canada, USA, Europe, Japan and South Korea, making recycling equally critical from economic and environmental perspectives.8 Sourcing and securing a sustainable supply chain for manufacturing LIBs means social issues are meaningful. The Democratic Republic of the Congo (DRC) holds 60 percent of the worlds' cobalt resource. The country has artisanal and small-scale mines (ASM) dominated by Chinese owned companies. This gives the Chinese LIB manufactures security over international manufacturers for cobalt supply. For years, human's rights groups have reported severe issues in mining operations in the DRC including, child labour, fatal accidents, and high corruption. Companies in need of cobalt supply are invested in improving the ASM standard for mine safety and child labor to ensure cobalt is mined responsibly.9
In order to enable LIB recycling, pathways for other types of batteries (NiMH, alkaline, and lead-acid) are modified to support the circular economy system. The components of LIBs, their structures, and their charge-storage mechanisms are used to design the recycling process.5 The current commercial approach to recycling NMC cathodes which offers the greatest extraction and lowest energy impacts, is the hydrometallurgical processing route.10 Several recycling facilities are operating globally and recovering critical metals like Li, Co, and Ni on a commercial scale using this approach. Although pyro- and hydro-metallurgical LIB recycling processes are commercialized, they aren't without fault. They involve high temperature smelting, pyrometallurgy, and the use of large quantities of chemicals, hydrometallurgy. Lately, research has focused on developing a greener recycling approach to decrease the environmental impact and operation costs associated with the current industrial methods. The promising direct recycling approach does not decompose the cathode active material into the elemental products which need to be completely re-manufactured like the pyro- and hydro-met routes do. Instead, the direct recycling approach applies “soft” means to induce relithiation of the cathode compound, e.g., NMC leaving the structure intact and re-functionalized.10 Hydrometallurgy is expected to play a key role towards this end as pointed out in the perspective section of the present paper. In this review a systematic compilation of the most important state-of-the-art hydrometallurgical recycling processes applicable to the dominant EV NMC cathode material family is presented by sourcing technical information from the recent patent literature and industrial news complementing the underlying chemistry discussion. Many of the presented processes are at the pilot scale, yet to be commercialized. Some of the processes described recover only cathode materials (Ni, Co, Li, Mn), while others are targeting a circular economy approach, recovering all components of the spent battery (graphite, Cu, Al, electrolyte, plastics etc.).
Fig. 1 Global electric passenger car stock, 2010–2020 (data sourced from ref. 12). |
According to the latest EV outlook report from BloombergNEF, 60 percent of new car sales worldwide must be electric by 2030 if a net-zero scenario is to be achieved.12
Demand for raw materials like graphite, lithium and cobalt is predicted to increase 500 percent by 2050, according to the World Bank.1 Several countries have revisited their list of critical materials in light of the EV era. The USA, EU, Japan, South Korea and Canada have released a list of critical minerals/metals.8
Table 1 shows 44 minerals/metals identified as critical, 9 of which are consistent between all countries: antimony, cobalt, gallium, indium, lithium, niobium, PGE/PGM, tungsten and vanadium. The metals lithium, nickel, cobalt, manganese, aluminum, and copper along with graphite that are required to manufacture LIBs are highlighted in green in Table 1.8 The EU Commission estimates that demand for cobalt and lithium will increase by a factor of 4 and 10, respectively, by 2030; and 10 and 40, respectively, by 2050.14 Cobalt is mainly mined as a by-product in nickel and copper mines. The supply of cobalt is of real concern because it is limited to a few countries such as DRC, Australia, Cuba, Philippines, Russia and Canada.15Fig. 2 shows the Global Cobalt Reserves which are dominated by DRC, 3.6 M tons, and Australia, 1.4 M tons. Although Australia has substantial reserves, they only mine 4 percent of the global production of cobalt. Due to the ethical and environmental concerns of mining in the DRC, the need to eliminate global dependence on this metal is crucial.9
Fig. 2 (Left) global cobalt reserves 2020, by country (in metric tons), (Right) global production of cobalt 2020, by country (% share of production) (data sourced from ref. 15). |
The raw materials needed to fulfill the supply that is being demanded to achieve net-zero emissions is not possible through mining alone. The current mines and projects that are under construction will only be able to produce 50 percent of the projected lithium and cobalt, and 80 percent of the required copper by 2030.16 Spent lithium-ion batteries contain between 5-20 weight percent of cobalt, 5–7 weight percent of lithium, and 5–7 weight percent of nickel, these concentrations are higher than what is naturally available from raw materials. Recycling is an economical solution to the raw material shortage.17
The estimation of material intensity of NMC lithium-ion battery packs (kg kW−1 h−1) has been analyzed by Argonne National Laboratory using their BatPaC modeling software with the main metrics presented in Table 2.18 The weight of lithium includes both the electrolyte and cathode. The cathode contains nickel, cobalt and manganese. Aluminum weights include current collectors, cell terminals, thermal conductors and module and battery enclosures. Copper weight is derived from the cell current collectors, terminals, thermal conductors and module and battery enclosures. The anode is responsible for the graphite weight.18
Material | NMC 111 | NMC 532 | NMC 622 | NMC 811 |
---|---|---|---|---|
Lithium | 0.141 | 0.136 | 0.118 | 0.1 |
Nickel | 0.351 | 0.508 | 0.531 | 0.6 |
Cobalt | 0.352 | 0.204 | 0.178 | 0.75 |
Manganese | 0.328 | 0.285 | 0.166 | 0.07 |
Aluminum | 3.11 | 3.07 | 3.017 | 2.921 |
Copper | 0.677 | 0.661 | 0.605 | 0.549 |
Graphite | 0.978 | 0.981 | 0.96 | 0.961 |
The change in NMC battery chemistry has evolved from high cobalt NMC 111 to high nickel NMC 811, from 2010 to predicted 2030, see Fig. 3. Cathode chemistry advancements can be credited for the reduction in cost of an EV battery.19
Fig. 3 NMC cathode chemistry evolution (data sourced from ref. 19). |
The average cost to produce a lithium-ion battery for an electric vehicle (EV) has significantly declined from $1200 per kW h in 2010, to $132 per kW h in 2021. S&P Global Platts has forecasted the EV battery manufacturing cost will reach price parity with ICE, at $100 per kW h by 2026.20 BloombergNEF has broken down the overall cost of a battery cell, see in Fig. 4. The cathode accounts for the half of the average cell cost, while the anode is 12 percent of the cell cost.
Fig. 4 The cost of a lithium-ion battery (reproduced from ref. 12 with permission from RCS, copyright 2021). |
The battery metals supply chain, particularly metals that make up the cathode, are experiencing pricing increases. Metals like lithium, nickel and cobalt have seen extreme increase in prices between 2020 and 2022, while manganese, aluminum, copper and graphite have also increased since 2020, refer to Table 3. Lithium pricing exploded by 496.7 percent between 2020 and 2021.21 Platts Analytics was expecting prices to stop rising in 2022 as the supply chain becomes more secure.20
The main advantage of hydrometallurgical recycling over pyrometallurgy is the recovery of high purity pay metals, Ni, Co, Mn, Li, with high recoveries, greater than 99 percent, low impurity content and a lower energy consumption (Fig. 6).17 Lithium is only recovered with hydrometallurgy, as lithium carbonate. Another benefit of the hydromet processing route is that it can adapt to a mixed cathode feed stock, eliminating the need to separate the spent batteries based on chemistry.10 The pyrometallurgical processing route, can only recover Co, Ni and Cu as alloys. The alloys require further refinement using hydrometallurgy.29
When recycling lithium-ion batteries, the most common hydrometallurgical method uses sulfuric acid and hydrogen peroxide. The following chemical equation, eqn (1), describes the leaching process.
2LiMO2(s) + 3H2SO4 + H2O2 → 2MSO4(aq) + Li2SO4 + 4H2O + O2 | (1) |
Cathode transition metals, such as Co and Mn, have low solubility because in a discharged cathode they are in the +3/+4 valence states. The strong M–O bonds make leaching difficult. Reducing the metals to a divalent state weakens the M–O bond allowing for effective leaching. It is understood that the hydrogen peroxide, H2O2, behaves as a reducing agent which converts Co3+ into the soluble Co2+ metal ion. The addition of peroxide has improved the leaching efficiency to greater than 95 percent.30 The by-product from the addition of H2O2 is water and oxygen gas. This reaction is graphically depicted in Fig. 7. This is a greener alternative than using other reducing agents such as sulfur dioxide, SO2, which produces sulfurous acid.
Fig. 7 Typical acid leach with reductant for NMC recycling, where yellow = sulfur, red = oxygen, white = hydrogen, M = metal (Ni–Mn–Co), M2+ = metal ions (divalent). |
Lithium leaching efficiency is directly correlated with the strength of acid. Displacement of Li+ with H+ allows for the lithium to become easily soluble during leaching.29 Once the leached metals, Li+, Ni2+, Mn2+, Co2+, Cu2+, Fe3+, and Al3+, are in solution, they are selectively addressed in the impurity removal and purification stage. Typically, multiple precipitation and solvent extraction stages are used to separate and purify the solution prior to the recovery of the metals. Metals such as Cu, Fe and Al, are considered to be impurities in this process. These metals can co-precipitate with value metals. The solubility of metal hydroxides in the NMC leach solution can be evaluated with the help of solubility diagrams, Fig. 8a and b. Sequential hydrolytic precipitation of metal hydroxides may be brought upon by Incremental pH adjustments following the solubility curves using a base, such as NaOH for example. The solution separation of Ni, Mn and Co is difficult to achieve using pH due to closeness of their respective solubility lines resulting in co-precipitation, and therefore a mixed metal hydroxide precipitate that requires further refinement by re-dissolution adding complexity and cost to the operation. Lithium hydroxide has a high solubility and thus often is precipitated with sodium carbonate, Na2CO3, as Li2CO3 (Fig. 8c and d). The fundamentals of metal ion compound precipitation from the standpoint of particle growth and cleanliness using supersaturation control methodologies are described by Demopoulos.31
Fig. 8 Solubility diagram for metal hydroxides at 25 °C (A) temperature effect on metal hydroxide solubility (B) solubility diagram for metal carbonates at 25 °C (C) and temperature effect on metal carbonate solubility (D) (reproduced from ref. 30 with permission from ACS, copyright 2022). |
The Ni–Mn–Co mixed metal solution following the impurity (Fe, Al, Cu) removal stage (by hydrolytic precipitation) is advanced to purification where the metals can be separated into individual purified solutions. Most hydromet processes use solvent extraction to separate the dissolved metals. The typical extraction reaction is given by, eqn (2), where (HA)2 is the dimer form of an acidic extractant like D2EHPA. The reverse reaction represents stripping of the metal ions into an acidic solution from which metal recovery is affected.
Maq2+ + Aorg− + 2(HA)2org ↔ MA2n3HAorg + Haq+ | (2) |
The selection of solvent extraction reagents (extractants) depends on composition of feedstock solution and the ionic state of key elements.39 Various extractants have been researched to separate and purify critical battery metals. The process uses time, pH, aqueous/organic (A/O) ratios, and concentration of extractant to control which metal ion will be selectively removed. Table 4 illustrates certain examples of different extraction conditions that have been reported. Many extractants have been used. By far as per well established practice of Co/Ni solvent extraction (consult for example the seminal book by G. M. Ritchey and A. W. Ashbrooke “Solvent Extraction: Principles & Applications to Process Metallurgy)” in commercial use for metallurgical nickel extraction plants the organophosphorus acid extractant family attracts the biggest interest.
Category | Extractant | Applications | Solution composition (g L−1) | Extraction conditions | Extraction efficiency | Ref. |
---|---|---|---|---|---|---|
Organic phosphoric acid extractant | • Mn extraction and impurity ions | Co: 0.175, Ni: 0.099, Mn: 5.269, Li: 1.248 | T: 300 s, pH: 5, A/O: 0.5, 20% vol D2EHPA, 70–75% saponification | Mn: 97% | 34 | |
• Co-extraction Co–Ni–Mn from Li | Co: 6.438, Ni: 0.089, Mn: 6.312, Li: 1.602 | T: 300 s, pH: 3.5, A/O: 1:1, 15% vol Mextral272P | Mn: 97.1% | 35 | ||
• Separate Ni and Co | ||||||
Organic phosphonic acid extractant | • Separate Ni | Ni: 2.54, Li: 4.82 | pH: 6.5, A/O: 1, 0.15 M PC88 A | Ni: 99.9% | 36 and 37 | |
• Separate Ni and Co | Co: 20, Ni: 0.5, Li: 2.5 | pH: 3.5, A/O: 1.5, 25% vol P507 | Co: 95%, <5% Ni and Li co-extraction | 38 and 36 | ||
Organic phosphinic acid extractant | • Separate Co | Co: 7.18, Ni: 4.29, Mn: 0.045, Li: 1.49 | T: 300 s, pH: 4.5, A/O: 1:1, 20% vol Ni loaded Mextral272P | Co: 97.8% | 39 | |
Blended extractants | • Separate Co/Li and Co/Ni | Co: 13.8, Ni: 0.015, Mn: 0.011, Li: 2.04 | pH: 5.5–6, A/O: 0.5, 0.4 M cyanex 272, 50% saponification | Co: 95–98%, ∼1% Ni extraction | 40 | |
D2EHPA + versatic 10 acid | — | Co: 11.4, Ni: 12.2, Mn: 11.7, Li: 5.3 | pH: 4.5, A/O: 1, 0.43 M D2EHPA and 0.7 M versatic 10 acid | Mn: 98.33%, Co: 1.06% Ni: 4.11% and Li: 0.25% co-extraction | 41 |
There are three types of organophosphorus acids (see their structures in Table 4): organic phosphoric, exemplified by D2EHPA (di-(2-ethylhexyl) phosphoric acid); organic phosphonic such as 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester, marketed as PC88A or P507; and organic phosphinic, bi(2,4,4-trimethylpentyl) phosphinic acid, marketed as Cyanex 272P or Mextral 272P. The organophosphorus acids may be graded according to their acidity (pKa) as follows: phosphoric > phosphonic > phosphinic. The more acidic the extractant the lower the pH at which can extract a metal, the faster the extraction rate, the lower the separation efficiency. For example, in Co/Ni separation, the extraction of Co follows the order D2EHPA > Phosphonic > Phosphinic, while the reverse happens in terms of Co/Ni separation efficiency Co: phosphinic > phosphonic > D2EHPA. A sample of extraction results with these reagents reported from NMC recycling studies is provided in Table 4.
The above results can be understood on the basis of the respective metal extraction equilibria which provide the selectivity series. The phosphinic acid (Cyanex 272/Mextral 272), which is commonly used to separate cobalt from nickel in sulphate media exhibits the selectivity series illustrated in Fig. 9.42
Fig. 9 Extraction equilibria of metals (in%) using cyanex 272 vs. pH in sulphate solutions (reproduced from ref. 43 with permission from KISTI, copyright 2015). |
Whereas D2EHPA is commonly used to separate Mn from Co, Ni and Li. The respective selectivity series can be seen in Fig. 10.
Fig. 10 Extraction equilibria of metals (in%) using D2EHPA vs. pH in sulphate solutions (reproduced from ref. 44 with permission from MDPI, copyright 2022). |
Metal separations are often enhanced by using a blend of two extractants, as is the example shown in Table 4, where a carboxylic acid extractant (Versatic 10, neodecanoic acid) was used in mixture with D2EHPA.41
On a pilot scale, Retriev has patented a process (Fig. S2†) that further treats and regenerates the cathode material. The black mass undergoes thermal treatment to remove the binder and a froth flotation treatment to remove the graphite anode. The metal oxides from the cathode material are recovered in the non-floated portion and regenerated with LiOH addition to correct lithium concentration and heating in a furnace (700–815 °C), milling and screening to achieve a particle size between 5 µm and 25 µm.48 The purity of the reactivated cathode material has not been reported but judging from their latest development activities involving the addition of hydrometallurgical purification steps it is deduced that this was not battery-grade. The latest addition has yet to be commercialized.
Umicore (Belgium) has the largest capacity, 7000 tonnes/year, amongst the commercial recycling plants using a hydrometallurgical method. The process recovers nickel and cobalt using a combination of pyrometallurgy and hydrometallurgy. Lithium and aluminum are lost as slag in the shaft furnace. There appears to be a two-stage leaching process (Fig. S3†) with the first stage (H2SO4) serving to remove selectively iron and copper impurities and the second stage in HCl solution allowing the separation of Ni and Co into Ni(OH)2 and CoCl2 products. A key environmental step of the Umicore process is the use of a high temperature step to treat waste gases, avoiding toxic emissions. Overall, the process seems to recover ∼70 percent of the metals, 10 percent graphite and 15 percent of the plastics. The earlier grade of the recovered metals was not suitable for new battery manufacturing,47 but this appears to have been overcome with process improvements reported from pilot scale testing.48
Brunp Recycling/CATL (China) process has an annual capacity to treat 30000 t per year of spent LIBS.48 The recycling process (Fig. S4†) includes discharging, thermal pre-treatment, mechanical treatment and complex hydrometallurgy (acid leaching with H2SO4 and HCl, solvent extraction for the separation of Ni and Co, crystallization of metal sulphate and chloride salts and a mixed intermediate hydroxide precipitate). The process, it is claimed to have a 99.3 percent metal recovery of nickel, cobalt and manganese, but this is difficult to verify. Additionally, it is unclear if the copper, aluminum and graphite is recovered in their process.
GEM Ltd, also known as Green Eco-Manufacturer Hi-Tech Co., Ltd, is located in China. The recycling company has an annual production of 5000 tonnes per year. The process begins with pre-treatment which sorts the major battery components using comminution. Metals such as, copper, aluminum, iron, cobalt and nickel, are separated by complex hydrometallurgical processing steps (of which little is known, Fig. S5†) and then synthesized into salts.6 The electrolyte is not recovered in this process.
Accurec (Germany) operates a LIB recycling process that includes thermal, mechanical, pyrometallurgy and hydrometallurgy steps (Fig. S6†). The recycling plant treats 3000 tonnes of lithium-ion batteries annually. Accurec has new technology being implemented in the current recycling process that will allow for the recovery of lithium and graphite.6
Nickelhütte Aue GmbH (NHA) has been recycling Li-ion batteries in Germany since 2011.6 Thermal pre-treatment, pyrometallurgy processing, and hydrometallurgy methods make up the recycling process. The flow diagram, shown in Fig. S7,† depicts NHA's process.49 The pyromet process smelts the spent batteries in a batch-wise-furnace to obtain Ni–Co–Mn matte product which subsequently is subjected to leaching to recover various metal salts. A rotary kiln is used to thermally pre-treat the batteries. Limited information is available regarding the specifics of the hydrometallurgy treatment. Unless there have been recent improvements the produced metal salts may not be of battery-grade but rather used in other fields like electroplating shops. The overall process capacity is 7000 tonnes per year.6
The Duesenfeld lithium-ion battery recycling process, LithoRec, completely discharges the battery packs before physical separation. As shown in Fig. S8,† the process isolates the electrode coatings and removes fluoride before leaching. The metals are then separated from graphite. Then lithium, cobalt, nickel and manganese are separated using various extraction methods. The metals are then purified and recovered as battery-grade salts, ready for new cathode application. The mechanical recycling rate is 72 percent, the recovery of electrolyte and graphite bring the overall recycling efficiency to 91 percent. The separator film and high boiler portion of the electrolyte make up the unrecycled 9 percent. The process located in Germany has an annual capacity of 3000 tonnes.6
SungEel HiTech, located in Korea, have a recycling plant capacity that treats 8000 tonnes of spent LIBS annually. The process scheme, shown in Fig. S9,† follows the general approach encountered in the previous plants starting with mechanical separation and followed by hydrometallurgical purification. There is not specific information available on the hydrometallurgy operations but judging from the products listed in the published flowsheet (Fig. 16) that includes salts and metal ingots, it is expected to be a complex one ranging from leaching to solution purification and recovery of metal salts by crystallization and metals by electrolysis. The company announced in 2020, it will be expanding operations to a new site that will triple the current capacity to 24000 tonnes per year.6,50
Dowa Holdings Co. Ltd (Japan) currently treats 1000 tonnes of spent LIBs a year. The process includes disassembly, thermal pre-treatment (rotary kiln), pyromet and hydromet processing. Details regarding the process technology, efficiency and recovery rates are not available.6
Fig. 11 Life cycle analysis for pyrometallurgy, hydrometallurgy and direct recycling (pyro, hydro, direct) (left) energy consumption, (middle) GHG emissions and (right) revenue from outputs, (reproduced from ref. 10 with permission from MDPI, copyright 2022). |
Fig. 12 Recupyl LIB recycling process (reproduced from ref. 48 with permission from MDPI, copyright 2021). |
In another development, Volkswagen (VW) adopted the LithoRec process from Duesenfeld and is now recycling LIBs on a pilot scale (Fig. S10†). This is the automaker's attempt to secure the raw materials needed and solve the supply chain shortage in house. The recycling of spent batteries will save VW from expensive procurement and disposal of raw materials. They have a target to recycle over 90 percent of spent batteries at the Salzgitter plant in Germany.52
Aalto University (Finland) has developed a comprehensive LIB recycling process that has been demonstrated in a laboratory scale (Fig. 13). The process targets 99 percent overall recovery using an improved pyro- and hydro-metallurgical method.53 The process involves mechanical separation of spent LIBs followed by screening of cathode material from metal foils.7 The cathode material is subjected to acid leaching with sulfuric acid because of the economic advantages. There is though provision for extra alkali leaching, using sodium hydroxide, in case recovery of rare earth elements as alkali double sulfates-is justified. The manganese is oxidatively precipitated with potassium permanganate. The iron impurity is removed with sodium hydroxide addition to pH 5.5. The cobalt, nickel and lithium continue into solvent extraction section. An important feature of the Aalto process is the treatment of sodium hydroxide and its in-plant utilization for REE precipitation to improve the overall economic and environmental impact.54
Fig. 13 Aalto University suggested NMC recycling process (reproduced from ref. 48 with permission from MDPI, copyright 2021). |
American Technology Company, located in the USA, uses the automated de-manufacturing of batteries (high separation of low-value by-products, targeted removal of contaminants), targeted hydrometallurgical proprietary chemical extraction train which extracts Li, Ni, Co and Mn and upgrades into battery grade (simplified IR, highly selective recovery of products, battery grade purity cathode products).55 The commercial recycling facility is under construction. The facility will treat 20000 tonnes of spent LIBs annually.
Lithion Recycling received $125 M in funding to build the first LIB recycling plant in Quebec, Canada. Commercialization of the plant is expected to begin in 2023, following the successful demonstration plant. The hydrometallurgical process operations are outlined in Fig. 14A, the leaching circuit, and in Fig. 14B, the metal separation steps. Leaching is done in H2SO4 followed by removal of Fe and Al impurities by neutralization and copper by sulfide precipitation before Li/Ni/Co/Mn are separated via a combination of precipitation and solvent extraction steps. Following solution purification, the cathode metals are recovered as lithium carbonate (by crystallization), nickel hydroxide (by neutralization) and cobalt metal (by electrowinning). The company claims their hydrometallurgical technology, has a recovery rate of 95 percent battery metals, which are purified for re-entry into the battery production chain56.
Fig. 14 Lithion recycling patented hydromet process (A) leaching circuit and (B) metal separation for recovery of all value metals and graphite from spent NMC.57 |
Li Cycle is another LIB recycling company located in Canada developing a spoke and hub operation for the North American market. The facility treats all types of LIBs and brings them from a charged state to inert product. A combination of mechanical separation and hydrometallurgical resource recovery techniques are used. The mechanical separation and size reduction produces a black mass free of foil components. Then the black mass follows a hydrometallurgical flowsheet for recovery of both cathode and anode materials. The graphite and copper sulfide are recovered in the first two stages of the patented process. Then manganese is recovered through solvent extraction and a secondary mixing stage as a carbonate. Cobalt and nickel are both recovered through solvent extraction and crystallization as sulphate salts. Sodium sulphate is then recovered through the crystallization process. Finally, lithium is treated and crystallized as a carbonate. Li-Cycle plans to have seven spokes and one hub in North America and Europe by the end of 2023. The Li Cycle process will have greater than ninety five percent recovery rate according to their patent.58
Hydrothermal treatment to induce re-lithiation10 of the de-lithiated NMC cathode is done in an autoclave with lithium hydroxide solution, to bring the Li back to ideal stoichiometry, 1.0.63 as per the following reaction (eqn (3)).
(3) |
Once the target Li concentration has been achieved, a final short annealing treatment is required to restore the layered crystal structure. To compensate for lithium loss during the high temperature annealing, generally 5 mol% excess lithium as carbonate salt is added.10
This method is non-destructive to the active NMC particles and regenerates their functionality in terms of lithium capacity and conductivity.64
An interesting variation of the direct recycling approach is the upcycling method which in addition to regenerating NMC it seeks to change its composition from low-Ni to Ni-rich stoichiometries, i.e., from NMC 111 to NMC 622. Upcycling (Ni-enrichment) typically is done during the thermal/annealing stage with the addition and mixing of extra Ni salt to hydrothermally re-lithiated NMC material.63 In the following section the latest hydromet-based direct recycling developments involving NMC cathodes are briefly introduced.
Fig. 16 American Manganese RecycLiCo™ process, a three compartment membrane electrodialysis cell for generating LiOH and H2SO4 (reproduced from ref. 67 with permission from Taylor and friends, copyright 2021). |
Battery Resources, now Ascend Elements, opened a 154000 square foot facility which can process 30000 tonnes of LIBs waste per year in Georgia, USA.68 Using a hydrometallurgical and direct recycling approach, the process has shown superior performance of recycled cathode materials.69 The patented Hydro-CathodeTM process claims that upcycled battery materials have 50 percent longer cycle life and 88 percent higher power capacity.70 The material from the lithium battery recycling stream undergoes an acid leach, which produces the leached solids. The solids are heated while being heated with a strong acid to remove any remaining cathode and separator components. By changing from aluminum oxide to aluminum sulfate, the strong acid eliminates any remaining aluminum oxide from the separator. Washing the acid-treated solids removes water-soluble impurities, such as aluminum sulfate formed when aluminum oxide and sulfuric acid interacted and produces graphite that is essentially pure (99%). The elemental composition of the cathode material is adjusted to suit industry needs. The process can either leave as a mixed NMC hydroxide (precursor), or a sinter (CAM) into various NMC chemistries (111, 532, 622, 811).71
OnTo Technology LLC has been a pioneer in direct recycling technology. Their patented process is called Cathode-HealingTM Direct Recycling. The process includes, extraction of electrolyte using supercritical CO2, shredding, mechanical electrode harvesting, flotation, Cathode-HealingTM, and rebuilding cells using recycled cathode and anode materials.53 The cathode healing method, classified as a direct recycling process, uses two-steps as described above, hydrothermal and heat treatment. The NMC cathode is regenerated by using lithium solution to add Li+ back into the structure, as well as repair the microstructure defects using heat.64 The regeneration mechanism of the cathode material structure is graphically illustrated in Fig. 17.
Fig. 17 OnTo technology's advanced battery recycling process for LIBs: cathode-healing™ impacts structure by mixing Ni2+ and Li+ to regenerate the full layered structure (reproduced from ref. 64 with permission from Elsevier, copyright 2019). |
Company | Location | Capacity (tonnes per year) | Method used to expose active materials | Method used to recover recyclable materials | Primary recovery material | Secondary recovery material | Lost material | References |
---|---|---|---|---|---|---|---|---|
Retriev technologies | Canada | 4500 | Wet mechanical treatment | Flotation, alkaline precipitation | Li2CO3, MeO | Steel, Cu, Co, Al, graphite | Plastics | 48 |
Umicore | Belgium | 7000 | Dismantling/physical separation | Acid leaching, solvent extraction | Co, Ni, Cu, Fe, CoCl2 | Slags: Al, Si, Ca, Fe, Li, Mn, REE | Electrolyte, plastics, graphite | 48 |
Brunp/CATL | China | 100000 | Discharging, thermal pre-treatment, mechanical treatment | Hydromet: H2SO4/H2O2, Na2S, or NaHS reductive acid leaching, SX | Ni–Mn–Co hydroxides, Co–Ni sulfates, Co chloride | Unknown | Unknown | 6 |
GEM Ltd | China | 30000 | Sorting, comminution | Hydrometallurgy, high temperature treatment | Co, Ni, Cu, Al, Fe | Unknown | Electrolyte, binder | 6 |
Accurec | Germany | 4000 | Sort, dismantle, milling, separation, agglomeration | Vacuum thermal treatment, reductive leaching H2SO4 | Li2CO3, Co-Alloy | Metallic alloy | Electrolyte, polymers, graphite | 48 |
Nickelhutte Aue GmbH | Germany | 3000 | Thermal pre-treatment | Pyro- and hydro- metallurgical treatment | Ni, Cu, Co | Slags | Unknown | 6 |
Duesenfeld | Germany | 2000 | Discharge, inert physical separation: two-stage crushing, air classification | Drying, calcination, leaching | Li2CO3, metal oxides | Al–Cu, plastics, electrolyte | Graphite | 6 and 48 |
SungEel HiTech | Korea | 8000 | Mechanical pre-treatment in water | Hydrometallurgical process | Co, Mn, Ni, Li2CO3 | Cu, Al | Unknown | 6 |
Dowa holdings | Japan | 1000 | Dismantle, thermal pre-treatment | Pyro- and hydro-metallurgical treatment | Co, Ni, Cu | Unknown | Unknown | 6 |
In many operations a common physical disassembly and separation approach is to mix several different battery components and types together. The black mass becomes cross contaminated with several impurity metals (aluminum, copper, titanium etc.) and organics (like the fluorine containing PVDF binder) that need to be treated downstream. Hydromet processing is effectively able to separate and purify the pay metals but in a very chemically intense manner. OnTo Technology has made advancements in this physical separation process by adding a supercritical CO2 process step to recover the organic electrolyte solvent. They have implemented a froth flotation process to separate anode and cathode material. This arguably provides a more suitable method by mitigating the anode and electrolyte from the downstream cathode recycling process that is more important economically.53
The cathode materials recovered in each of the processes listed in Table 5 only account for 50 percent of the total battery material. Valuable components are lost such as graphite, which makes up 12 percent (0.978 kg kW−1 h−1) of the total for a NMC 111 battery, and aluminum and copper, which account for 3.11 kg kW−1 h−1 and 0.677 kg kW−1 h−1 respectively.73 There is much need for improvement in the current LIB recycling practice by embracing circular economy approaches. Among the challenges of the current hydromet processes are manganese oxidative state control, fluorine (electrolyte) recovery, recovery of battery-grade lithium, nickel, and cobalt salts and graphite in a marketable form.10
A closed-loop recycling process of lithium-ion batteries could save up to 51.3 percent of mined raw materials.74 The environmental impacts can be lowered with a 70 percent reduction in CO2 emissions and up to 70 percent energy consumption savings according to the EverBatt model, developed by Argonne National Laboratory.51 Emerging recycling technology, direct recycling/upcycling, will need more research to determine the realization of commercialization and compete with current hydro-pyro- metallurgy processes. Hydrometallurgical-based unit operations like hydrothermal relithiation10,75 or electrochemical cathodic relithiation76 are examples of how direct recycling can benefit by innovative process integration. Direct recycling technology though still doesn't address one of the major challenges with LIB recycling, the need to sort based on battery chemistry. There is no evidence that this process can handle a “mixed cathode” feed stock.51 Until improvements to battery sorting, state of health (SOH), state of charge (SOC), is implemented through policy and mandates, the commercial recycling processes will not be 100% free of producing harmful by-products or additional toxins that need to be treated.77 There has not been enough research on the long term affects and environmental risk associated with metal and organic contaminants building up in the processing plant. The new state-of-the-art recycling technologies incorporating hydrometallurgical innovations including direct recycling are summarized in Table 6.
Company | Location | Capacity (tonnes per year) | Stage | Method used to expose active materials | Method used to recover recyclable materials | Primary recovery material | Secondary recovery material | Lost material | Reference |
---|---|---|---|---|---|---|---|---|---|
Recupyl | France | 110 | Active | Dry mechanical treatment under inert atmosphere | H2SO4/H2O2 reductive acid leach, selective precipitation | Li, metal oxides, graphite | Steel: Cu/Al, plastic | Unknown | 31 and 32 |
Volkswagen | Germany | Unknown | Pilot scale | Physical separation, shredding, drying, sieving | Hydro-metallurgy | Co, Ni, Mn, Li | Steel, separator, Al, Cu | Electrolyte, plastics | 19 |
Aalto University | Finland | Unknown | Concept laboratory process | Shredding, sieving | Al smelter, leaching | CoC2O4, Al–Cu Alloy | Jarosite, MnO2, Cu(OH)2, Li–Ni solution | Graphite, binder, plastic, Cu, water | 48 and 21 |
American battery technology | USA | 20000 | Under construction | Automated de-manufacturing process | Hydro-metallurgy: Impurity removal | Unknown | Unknown | Unknown | 22 |
Lithion | Canada | 5000 | Under construction | Physical separation, shredding, drying, sieving | Hydro-metallurgy, distillation | Ni, Co, Mn, Li | Unknown | Unknown | 23 and 24 |
Li-Cycle | Canada | 5000 | Planned | Mechanical separation, size reduction | Hydro-metallurgy | Ni, Co, Mn, Li | Steel: Cu/Al, graphite | Electrolyte, plastics | 25 |
American manganese | Canada | 180 | Planned | Shred, separate | Direct recycling/Hydro upcycling | NMC hydroxide, Li2CO3 | Unknown | Unknown | 26 and 27 |
Battery resourcers | USA | 30000 | Planned | Discharge, shred, mag sep, sieve, dense media, ambient | Hydromet/Direct recycling: NaOH, H2O2, H2SO4 and Na2CO3 | Li2CO3, cathode powder | Ferrous metals | Electrolyte | 48 |
OnTo technology LLC | USA | Unknown | Unknown | Supercritical CO2, physical disassembly | Hydromet/Direct recycling: Heat treatment, LiOH leaching | Cathode powder, Li2CO3 | Electrolyte, graphite, Fe, Al, Cu, plastics | Unknown | 20, 30 and 33 |
To achieve effective and sustainable recycling of lithium-ion batteries (LIBs), several key areas of R&D must be considered. Reducing pollutant emissions and adopting non-toxic solvents are crucial for minimizing environmental impact.78 Recycling efforts should go beyond metal recovery and also reclaim electrolytes, separators, and negative carbon materials.79 As the cobalt content in cathodes decreases, current recycling processes may become uneconomical, necessitating advancements in recycling technologies.80 The current and state of the art R&D processes shown in both Tables 5 and 6 are not without deficiencies. Technology innovation is essential to develop low-waste and high-efficiency processes. Environmental and safety aspects should not be overlooked, and efforts should focus on reducing heavy metal content, switching to environmentally friendly binders and electrolytes, and treating and mitigating wastewater, gas, and residues produced during the recycling process to minimize emissions.81
Success in battery recycling will also depend on non-technical factors, such as implementing legislation and policies for proper collection, transportation, and storage of end-of-life batteries. To ensure proper tracking and accountability, governments should implement a battery passport system that monitors each stage of the recycling process and ensures compliance with recycling responsibilities.80
Direct recycling methods should ensure high purity of recovered materials by carefully analyzing cell component chemistries, state of charge (SOC), and state of health (SOH) before disassembly. Fan et al. emphasize the need for technical advancements, including automated disassembly, simplified recycling processes, and the development of new battery chemistries with reduced dependence on critical minerals.81
In conclusion, the development of physical recycling processes, including stabilization, opening, and separation, is crucial for sustainable LIB recycling. Separating the black mass following cell disassembly enables direct recycling and reduces waste, contributing to a more environmentally friendly and efficient recycling approach.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3su00142c |
This journal is © The Royal Society of Chemistry 2023 |