ELECTROCHEMICAL LITHIUM RECOVERY SYSTEM
20240014456 ยท 2024-01-11
Assignee
Inventors
Cpc classification
International classification
Abstract
Disclosure relates to an electrochemical lithium recovery system, and the electrochemical lithium recovery system is characterized by having a first flow electrode module that selectively extracts lithium ions from an object solution containing a waste battery active material by electrical attraction, and a second flow electrode module recovering the lithium ions extracted by the first flow electrode module, by the electric repulsive force. Accordingly, the electrochemical lithium recovery system does not require a high temperature treatment process, does not require a large amount of chemicals, and can ensure high recovery efficiency.
Claims
1. An electrochemical lithium recovery system comprising: a first flow electrode module selectively extracting lithium ions from an object solution containing a waste battery active material by electrical attraction; and a second flow electrode module recovering the lithium ions extracted by the first flow electrode module, by an electric repulsive force.
2. The electrochemical lithium recovery system of claim 1, wherein the first flow electrode module comprises: a first anode channel in which a first front end fluid flows and to which anode is applied; a first cathode channel in which a second front end fluid flows and to which cathode is applied; a first flow channel in which the object solution flows; and a first front end ion exchange membrane dividing the first cathode channel and the first flow channel from each other, and allowing selectively penetration of 1 valent ions so that the lithium ions in the object solution are permeatible towards the second front end fluid, wherein, by electrical attraction of the first cathode channel, the lithium ions of +1 valent penetrate through the first front end cation exchange membrane.
3. The electrochemical lithium recovery system of claim 2, wherein the second flow electrode module further comprises: a second anode channel into which the second front end fluid discharged from the first cathode channel is introduced and flows therein, and to which anode is applied; a second cathode channel in which a second rear end fluid flows and to which cathode is applied; a second flow channel in which treated water flows; and a first rear end ion exchange membrane dividing the second anode channel and the second flow channel from each other, wherein, by an electric repulsive force of the second anode channel, the lithium ions penetrate through the first rear end ion exchange membrane to be recovered to the treated water.
4. The electrochemical lithium recovery system of claim 3, wherein the second front end fluid flowing in the first cathode channel includes a manganese oxide solution; and the lithium ions penetrating through the first front end ion exchange membrane are absorbed to a manganese oxide in the second front end fluid to be introduced to the second anode channel.
5. The electrochemical lithium recovery system of claim 3, wherein the object solution is created by leaching the waste battery active material into a sulfuric acid solution; and lithium hydroxide contained in the waste battery active material reacts in the sulfuric acid solution to be introduced into the first flow channel in a lithium sulfate state.
6. The electrochemical lithium recovery system of claim wherein the first flow electrode module comprises a second front end ion exchange membrane dividing the first anode channel and the first flow channel from each other; and by electrical attraction of the first anode channel, sulfuric acid ions in the object solution penetrate through the second front end ion exchange membrane to be introduced into the first front end fluid.
7. The electrochemical lithium recovery system of claim 6, wherein the first front end fluid discharged from the first anode channel is introduced into the second cathode channel, and serves as the second rear end fluid in the second cathode channel.
8. The electrochemical lithium recovery system of claim 7, wherein the second flow electrode module further comprises: a second rear end ion exchange membrane dividing the second anode channel and the second flow channel from each other; and a bi-polar ion exchange membrane dividing the second flow channel into a first recovery channel at the side of the second anode channel, and a second recovery channel at the side of the second cathode channel, wherein, by an electric repulsive force of the second anode channel, the lithium ions penetrating through the first rear end ion exchange membrane are introduced into the first recovery channel; and by an electric repulsive force of the second cathode channel, the sulfuric acid ions in the second rear end fluid penetrate through the second rear end ion exchange membrane to be introduced into the second recovery channel.
9. The electrochemical lithium recovery system of claim 8, wherein the sulfuric acid ions recovered through the second recovery channel are reused to create the object solution.
10. The electrochemical lithium recovery system of claim 3, wherein the first front end fluid contains activated carbon.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0027]
[0028]
[0029]
DETAILED DESCRIPTION
[0030] The above and other objectives, features, and advantages of embodiments of the present disclosure, and a method of achieving them will be more clearly understood with reference to the embodiments described below in detail in conjunction with the accompanying drawings. However, the present disclosure is not limited to the following embodiments, and can be embodied in various forms different from each other, and embodiments of the present disclosure are presented to make complete disclosure of the present disclosure and help those who are ordinarily skilled in the art to which the present disclosure belongs understand the spirit and scope of the present disclosure. The present disclosure is only defined by the scope of the claims. The same reference numerals are used throughout the specification to designate the same or similar components.
[0031] Hereinbelow, embodiments of the present disclosure will be described in detail with reference to accompanying drawings.
[0032]
[0033] Referring to
[0034] In the embodiment of the present disclosure, the first flow electrode module 100 and the second flow electrode module 200 are configured based on a flow-electrode capacitive deionization (FCDI) system.
[0035] At this point, the first flow electrode module 100 selectively extracts lithium ions from an object solution containing a waste battery active material AM, by electrical attraction, and the second flow electrode module 200 may recover the lithium ions extracted by the first flow electrode module 100, by an electric repulsive force.
[0036] The embodiment of the present disclosure illustrates that the waste battery active material AM, i.e., an active material AM extracted from a waste battery is leached into a storage tank L in which a sulfuric acid solution is stored to create the object solution, and the created object solution is introduced into the first flow electrode module 100.
[0037] At this point, lithium is contained in the waste battery active material AM in the form of lithium hydroxide (LiOH), and is converted into sulfuric acid lithium (Li2SO2) in the sulfuric acid solution and is introduced into the first flow electrode module 100.
[0038]
[0039] Referring to
[0040] According to the embodiment of the present disclosure, the object solution flows into the first flow channel 150. At this point, the first flow channel 150 is formed by the first front end ion exchange membrane 132 and the second front end ion exchange membrane 112.
[0041] The first anode channel 113 is formed between the second front end ion exchange membrane 112 and a first anode panel 111. At this point, first front end fluid flows into the first anode channel 113, and positive power is applied through the first anode panel 111. At this point, the first front end fluid may be activated carbon (AC) solution.
[0042] The first cathode channel 133 is formed between the first front end ion exchange membrane 132 and a first cathode panel 131. At this point, second front end fluid flows into the first cathode channel 133, and negative power is applied through the first cathode panel 131.
[0043] According to the embodiment of the present disclosure, the first front end ion exchange membrane 132 divides the first cathode channel 133 and the first flow channel 150 from each other. Furthermore, the first front end ion exchange membrane 132 allows selectively penetration of 1 valent ions. The embodiment of the present disclosure illustrates that a cation exchange membrane is applied as the first front end ion exchange membrane 132 so that the lithium ions, i.e., +1 valent ions, may penetrate through the first front end ion exchange membrane 132.
[0044] According to the above-described structure, when power is applied to through the first anode panel 111 and the first cathode panel 131, the second front end fluid flowing into the first cathode channel 133 have () charge, and an ionic substance having (+) charge is moved towards the first cathode channel 133 by the electrical attraction according to the () charge.
[0045] As shown in
[0046] At this point, as () charge is applied to the first cathode channel 133, the ionic substance having (+) charge is moved to the first cathode channel 133, and since the first front end ion exchange membrane 132 allows selectively penetration of only +1 valent ions, only the lithium ions, i.e., the +1 valent ions, penetrate the first front end ion exchange membrane 132 to be moved to the first cathode channel 133.
[0047] According to the above-described configuration, selective extraction of the lithium ions from the waste battery active material AM including various substances is possible.
[0048] At this point, the embodiment of the present disclosure illustrates that the second front end fluid flowing the first cathode channel 133 includes a manganese oxide (MO) solution. The manganese oxide MO has high absorbability with respect to the lithium ions, and the lithium ions penetrating the first front end ion exchange membrane 132 are absorbed to the manganese oxide MO in the second front end fluid to flows LMO. Therefore, selective extraction of lithium ions, and extraction efficiency thereof can be improved.
[0049] Meanwhile, according to the embodiment of the present disclosure, the second front end ion exchange membrane 112 may consist of an anion exchange membrane allowing selective penetration of anion.
[0050] Furthermore, by electrical attraction of the first anode channel 113 according to (+) charge applied to the first anode channel 113, the sulfuric acid ions in the object solution may penetrate the second front end ion exchange membrane 112 to be introduced into the first front end fluid. At this point, description of the sulfuric acid ions introduced into the first front end fluid will be described below.
[0051] Hereinbelow, referring to
[0052] According to the embodiment of the present disclosure, the second flow electrode module 200 may include a second anode channel 213, a second cathode channel 233, a second flow channel 250, and a first rear end ion exchange membrane 212. Furthermore, the second flow electrode module 200 may include a second rear end ion exchange membrane 232 and a bi-polar ion exchange membrane 253.
[0053] According to the embodiment of the present disclosure, the treated water flows into the second flow channel 250. Furthermore, the first flow channel 150 is formed by the first rear end ion exchange membrane 212 and the second rear end ion exchange membrane 232.
[0054] The second anode channel 213 is formed between the first rear end ion exchange membrane and the second anode panel 211. At this point, the second front end fluid discharged from the first cathode channel 133 is introduced into the second anode channel 213 and flows therein. As described above, the lithium ions are extracted and flow together with the second front end fluid, and may be moved while being absorbed to the manganese oxide MO. At this point, positive power is applied to the second anode channel through the second anode panel 211.
[0055] The second cathode channel 233 is formed between the second rear end ion exchange membrane 232 and a second cathode panel 231. At this point, the second rear end fluid flows into the second cathode channel 233, and negative power is applied through the second cathode panel 231.
[0056] The embodiment of the present disclosure illustrates that the first front end fluid discharged from the first anode channel 113 is introduced into the second cathode channel 233. In other words, the first front end fluid discharged from the first anode channel 113 serves as the second rear end fluid flowing through the second cathode channel 233.
[0057] According to the embodiment of the present disclosure, the first rear end ion exchange membrane 212 divides the second anode channel 213 and the second flow channel 250 from each other. Furthermore, the first rear end ion exchange membrane 212 may allow selectively penetration of the 1 valent ions. The embodiment of the present disclosure illustrates that the cation exchange membrane is applied as the first rear end ion exchange membrane 212 so that the lithium ions, i.e., the +1 valent ions, may penetrate through the first rear end ion exchange membrane 212.
[0058] According to the above-described structure, when power is applied through the second anode panel 211 and the second cathode panel 231, the second front end fluid flowing into the second anode channel 213 have (+) charge, and an ionic substance having (+) charge is moved towards the second cathode channel 233 by the electrical repulsive force according to the (+) charge. In other words, the lithium ions of (+) charge extracted from the first flow electrode module 100 penetrate through the first rear end ion exchange membrane 212 to be moved to the second flow channel 250 in which the treated water flows.
[0059] Therefore, as the treated water of the second flow channel 250 is recovered, recovery of the lithium ions is possible.
[0060] Meanwhile, the second rear end ion exchange membrane 232 divides the second anode channel 213 and the second flow channel 250 from each other. At this point, the second rear end ion exchange membrane 232 may be composed of the anion exchange membrane through which anions selectively penetrate.
[0061] It is illustrated that the bi-polar ion exchange membrane 253 according to the embodiment of the present disclosure divides the second flow channel 250 into a first recovery channel 251 at the side of the second anode channel 213 and a second recovery channel 252 at the side of the second cathode channel 233.
[0062] Accordingly, an electric repulsive force of the second anode channel 213 allows the lithium ions penetrating through the first rear end ion exchange membrane 212 to be introduced into the first recovery channel 251. Furthermore, an electric repulsive force of the second cathode channel 233 allows the second rear end fluid, i.e., the sulfuric acid ions in the first front end fluid discharged from the first anode channel 113, to penetrate through the second rear end ion exchange membrane 232 to be introduced into the second recovery channel 252.
[0063] Therefore, as the treated water flowing in the first recovery channel 251 is recovered, recovery of the lithium ions is possible, and as the treated water flowing in the second recovery channel 252 is recovered, recovery of the sulfuric acid ions is possible.
[0064] At this point, the treated water containing the sulfuric acid ions recovered through the second recovery channel 252 is reused to generate the object solution, thereby reducing the amount of use of sulfuric acid used for generating the object solution.
[0065] Through the above-described process, the treated water containing the lithium ions may be received in a recovery tank 300. Then, when carbonate is injected into the recovered treated water, lithium recovery in the form of lithium carbonate is possible.
[0066] Although the embodiments of the present disclosure have been disclosed for illustrative purposes, those who are ordinarily skilled in the art to which the present disclosure belongs will appreciate that the embodiments can be modified without departing from the scope and sprit of the present disclosure. The scope of the present disclosure should be defined by the accompanying claims and equivalents thereof.
DESCRIPTIONS FOR THE REFERENCE NUMBER OF THE FIGURES
[0067] 10: electrochemical lithium recovery system [0068] 100: first flow electrode module [0069] 111: first anode panel [0070] 112: second front end ion exchange membrane [0071] 113: first anode channel [0072] 131: first cathode panel [0073] 132: first front end ion exchange membrane [0074] 133: first cathode channel [0075] 150: first flow channel [0076] 200: second flow electrode module [0077] 211: second anode panel [0078] 212: first front end ion exchange membrane [0079] 213: second anode channel [0080] 231: second cathode panel [0081] 232: second rear end ion exchange membrane [0082] 233: second cathode channel [0083] 250: second flow channel [0084] 251: first recovery channel [0085] 252: second recovery channel [0086] 253: bi-polar ion exchange membrane [0087] 300: recovery tank