WO2022220477A1 - 고회수율의 리튬 농축 용액 제조 방법 및 이를 이용한 리튬 화합물의 제조 방법 - Google Patents
고회수율의 리튬 농축 용액 제조 방법 및 이를 이용한 리튬 화합물의 제조 방법 Download PDFInfo
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- WO2022220477A1 WO2022220477A1 PCT/KR2022/004946 KR2022004946W WO2022220477A1 WO 2022220477 A1 WO2022220477 A1 WO 2022220477A1 KR 2022004946 W KR2022004946 W KR 2022004946W WO 2022220477 A1 WO2022220477 A1 WO 2022220477A1
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- WIPO (PCT)
- Prior art keywords
- lithium
- compound
- solution
- lithium compound
- sulfate
- Prior art date
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- 150000002642 lithium compounds Chemical class 0.000 title claims abstract description 99
- 238000011084 recovery Methods 0.000 title claims abstract description 47
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 22
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims abstract description 109
- 229910001416 lithium ion Inorganic materials 0.000 claims abstract description 108
- 238000000034 method Methods 0.000 claims abstract description 66
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 53
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000002904 solvent Substances 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000243 solution Substances 0.000 claims description 105
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims description 70
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 claims description 39
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 claims description 39
- 239000007864 aqueous solution Substances 0.000 claims description 37
- 239000002994 raw material Substances 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 claims description 24
- 239000007788 liquid Substances 0.000 claims description 24
- 238000001027 hydrothermal synthesis Methods 0.000 claims description 22
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 claims description 21
- 150000001875 compounds Chemical class 0.000 claims description 18
- 230000001376 precipitating effect Effects 0.000 claims description 17
- 239000002699 waste material Substances 0.000 claims description 17
- 239000011734 sodium Substances 0.000 claims description 16
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 claims description 13
- 229910052808 lithium carbonate Inorganic materials 0.000 claims description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 12
- 239000010406 cathode material Substances 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 claims description 10
- 238000010612 desalination reaction Methods 0.000 claims description 9
- 238000005805 hydroxylation reaction Methods 0.000 claims description 8
- 239000012528 membrane Substances 0.000 claims description 8
- 238000005406 washing Methods 0.000 claims description 8
- 229910018119 Li 3 PO 4 Inorganic materials 0.000 claims description 7
- 229910010093 LiAlO Inorganic materials 0.000 claims description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 6
- 238000004064 recycling Methods 0.000 claims description 6
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 5
- 229910001386 lithium phosphate Inorganic materials 0.000 claims description 5
- 229910003002 lithium salt Inorganic materials 0.000 claims description 5
- 159000000002 lithium salts Chemical class 0.000 claims description 5
- 239000011777 magnesium Substances 0.000 claims description 5
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 3
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims description 3
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims description 3
- 235000011130 ammonium sulphate Nutrition 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- GBAOBIBJACZTNA-UHFFFAOYSA-L calcium sulfite Chemical compound [Ca+2].[O-]S([O-])=O GBAOBIBJACZTNA-UHFFFAOYSA-L 0.000 claims description 3
- 235000010261 calcium sulphite Nutrition 0.000 claims description 3
- FAYYUXPSKDFLEC-UHFFFAOYSA-L calcium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [Ca+2].[O-]S([O-])(=O)=S FAYYUXPSKDFLEC-UHFFFAOYSA-L 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- YDIQKOIXOOOXQQ-UHFFFAOYSA-H dialuminum;trisulfite Chemical compound [Al+3].[Al+3].[O-]S([O-])=O.[O-]S([O-])=O.[O-]S([O-])=O YDIQKOIXOOOXQQ-UHFFFAOYSA-H 0.000 claims description 3
- FGRVOLIFQGXPCT-UHFFFAOYSA-L dipotassium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane Chemical compound [K+].[K+].[O-]S([O-])(=O)=S FGRVOLIFQGXPCT-UHFFFAOYSA-L 0.000 claims description 3
- 239000011790 ferrous sulphate Substances 0.000 claims description 3
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 3
- 230000014509 gene expression Effects 0.000 claims description 3
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 3
- FPNCFEPWJLGURZ-UHFFFAOYSA-L iron(2+);sulfite Chemical compound [Fe+2].[O-]S([O-])=O FPNCFEPWJLGURZ-UHFFFAOYSA-L 0.000 claims description 3
- RUTXIHLAWFEWGM-UHFFFAOYSA-H iron(3+) sulfate Chemical compound [Fe+3].[Fe+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O RUTXIHLAWFEWGM-UHFFFAOYSA-H 0.000 claims description 3
- LIRDHUDRLFDYAI-UHFFFAOYSA-H iron(3+);trisulfite Chemical compound [Fe+3].[Fe+3].[O-]S([O-])=O.[O-]S([O-])=O.[O-]S([O-])=O LIRDHUDRLFDYAI-UHFFFAOYSA-H 0.000 claims description 3
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 3
- 229910000360 iron(III) sulfate Inorganic materials 0.000 claims description 3
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 claims description 3
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 3
- CQDMJJVHDPDPHO-UHFFFAOYSA-L magnesium;dioxido-oxo-sulfanylidene-$l^{6}-sulfane;hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[O-]S([O-])(=O)=S CQDMJJVHDPDPHO-UHFFFAOYSA-L 0.000 claims description 3
- JESHZQPNPCJVNG-UHFFFAOYSA-L magnesium;sulfite Chemical compound [Mg+2].[O-]S([O-])=O JESHZQPNPCJVNG-UHFFFAOYSA-L 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 3
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 3
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 claims description 3
- 235000011151 potassium sulphates Nutrition 0.000 claims description 3
- 235000019252 potassium sulphite Nutrition 0.000 claims description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 3
- 235000011152 sodium sulphate Nutrition 0.000 claims description 3
- 235000010265 sodium sulphite Nutrition 0.000 claims description 3
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 claims description 3
- 235000019345 sodium thiosulphate Nutrition 0.000 claims description 3
- 239000003513 alkali Substances 0.000 abstract description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 6
- 238000002386 leaching Methods 0.000 abstract description 6
- 238000005265 energy consumption Methods 0.000 abstract description 5
- 239000012535 impurity Substances 0.000 abstract description 4
- 238000001228 spectrum Methods 0.000 description 15
- 238000003795 desorption Methods 0.000 description 12
- 238000001179 sorption measurement Methods 0.000 description 12
- 238000001556 precipitation Methods 0.000 description 11
- 239000002244 precipitate Substances 0.000 description 8
- 238000000746 purification Methods 0.000 description 7
- TXKMVPPZCYKFAC-UHFFFAOYSA-N disulfur monoxide Inorganic materials O=S=S TXKMVPPZCYKFAC-UHFFFAOYSA-N 0.000 description 6
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 6
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 6
- 239000010413 mother solution Substances 0.000 description 5
- 229910003514 Sr(OH) Inorganic materials 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- GLXDVVHUTZTUQK-UHFFFAOYSA-M lithium hydroxide monohydrate Substances [Li+].O.[OH-] GLXDVVHUTZTUQK-UHFFFAOYSA-M 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 239000000920 calcium hydroxide Substances 0.000 description 2
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000011033 desalting Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000002336 sorption--desorption measurement Methods 0.000 description 2
- 238000004448 titration Methods 0.000 description 2
- 229910017119 AlPO Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229910003003 Li-S Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 150000004645 aluminates Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000002242 deionisation method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- RKGLUDFWIKNKMX-UHFFFAOYSA-L dilithium;sulfate;hydrate Chemical compound [Li+].[Li+].O.[O-]S([O-])(=O)=O RKGLUDFWIKNKMX-UHFFFAOYSA-L 0.000 description 1
- BBLSYMNDKUHQAG-UHFFFAOYSA-L dilithium;sulfite Chemical compound [Li+].[Li+].[O-]S([O-])=O BBLSYMNDKUHQAG-UHFFFAOYSA-L 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- PQVSTLUFSYVLTO-UHFFFAOYSA-N ethyl n-ethoxycarbonylcarbamate Chemical compound CCOC(=O)NC(=O)OCC PQVSTLUFSYVLTO-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000002803 fossil fuel Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- -1 lithium hydroxide anhydride Chemical class 0.000 description 1
- 229940040692 lithium hydroxide monohydrate Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D15/00—Lithium compounds
- C01D15/02—Oxides; Hydroxides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D15/00—Lithium compounds
- C01D15/08—Carbonates; Bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D15/00—Lithium compounds
- C01D15/06—Sulfates; Sulfites
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/54—Reclaiming serviceable parts of waste accumulators
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2002/00—Crystal-structural characteristics
- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/40—Electric properties
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P10/00—Technologies related to metal processing
- Y02P10/20—Recycling
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
- Y02W30/00—Technologies for solid waste management
- Y02W30/50—Reuse, recycling or recovery technologies
- Y02W30/84—Recycling of batteries or fuel cells
Definitions
- the present invention relates to a method for producing a lithium concentrated solution having a high recovery rate and a method for producing a lithium compound using the same.
- the present invention relates to a method for preparing a lithium ion concentrated solution and a lithium compound prepared thereby.
- Raw materials for obtaining lithium ions include lithium salt lake, waste liquid from lithium compound manufacturing process, lithium secondary battery cathode material washing water, and lithium secondary battery recycling process waste liquid. There is a problem in that the recovery efficiency of lithium ions is lowered.
- a method for producing lithium carbonate or lithium hydroxide which are lithium compounds for lithium ion recovery from a low concentration lithium solution (Li + conc. ⁇ 1,000 ppm)
- an adsorption method, solvent extraction method, precipitation method, etc. are applied to concentrate it into a high concentration lithium solution. , it is generally produced through carbonation or hydroxylation of a lithium solution from which impurities have been removed through separation/purification processes.
- Another commercialization process for producing such a lithium compound for lithium ion recovery is calcining and roasting a lithium-containing mineral, followed by water leaching to produce a high-concentration lithium solution or a natural salt lake (about 1,000 ppm) containing lithium ions.
- a method of preparing lithium carbonate and lithium hydroxide through carbonation and hydroxide reaction after preparing a high-concentration lithium solution through evaporation and concentration is a common method.
- lithium ion compounds Recently, many attempts have been made to recover lithium resources in the form of lithium ion compounds from low-concentration lithium salt lake and lithium waste liquid, lithium compound manufacturing process waste, cathode material washing water, lithium secondary battery recycling process waste, etc. to be.
- a high-concentration lithium solution manufacturing process is required in the lithium compound manufacturing process and occupies the highest proportion in the process, but economic feasibility is still not secured in the high-concentration lithium solution manufacturing stage.
- Lithium carbonate and lithium hydroxide are used as reactants in manufacturing for medium and large capacity, and a water washing process is essential after manufacturing the cathode material.
- the lithium waste liquid generated during washing has a lithium ion concentration of about 1000 ⁇ 1500 mg/L, and it is expected that the amount of washing water generated by the cathode material will increase as the production of cathode material rapidly increases.
- an insoluble lithium compound is prepared into a lithium sulfate or lithium chloride solution using an acid solution, and impurities are separated using an alkali solvent such as CaO, NaOH, and the lithium solution under alkaline conditions.
- an alkali solvent such as CaO, NaOH
- a method of producing lithium carbonate and lithium hydroxide through carbonation and hydroxide reaction by conversion is common.
- this method uses a strong acid solution when preparing a high-concentration lithium solution, it is inevitable to use an excess alkali solvent in the subsequent process, and there is a problem in that it has an environmental load in which excess waste sediment and waste liquid are discharged.
- the present invention can recover lithium ions with a high recovery rate by preparing a high-concentration lithium sulfate solution, and at the same time, a method for producing an eco-friendly lithium compound for recovering lithium ions because the amount of use of an alkali solvent is remarkably small and energy consumption can be reduced, and
- An object of the present invention is to provide a lithium compound for recovering lithium ions formed by
- the present invention comprises the steps of 1) precipitating an insoluble lithium compound in a raw material solution containing lithium ions;
- It provides a method for preparing a lithium compound with a high recovery comprising a.
- A is one or more cations selected from magnesium, calcium, sodium, potassium, iron (Fe), ammonium and aluminum, y is an integer of 2 to 4, and z is 1 or 3.
- the insoluble lithium compound may be at least one selected from lithium phosphate (Li 3 PO 4 ), lithium fluoride (LiF), and lithium aluminate (LiAlO 2 ).
- step 1) a precipitating agent is added to the raw material solution to precipitate an insoluble lithium compound
- the equivalent ratio of the precipitating agent may be added to be 0.5-5 with respect to the lithium ion of the raw material solution.
- step 1) is
- MCDI membrane capacitive desalination process
- 1-2) precipitating an insoluble lithium compound from the raw material solution may include.
- the low-concentration lithium solution may be derived from at least one selected from lithium salt lake, waste liquid from a lithium compound manufacturing process, lithium secondary battery cathode material washing water, and lithium secondary battery recycling process waste liquid.
- the lithium ion concentration of the low concentration lithium solution and the raw material solution in step 1-1) may satisfy the following relational expressions (1) and (2).
- step 1-1) can be repeatedly performed
- the compound represented by the general formula 1 in step 2) is magnesium sulfate (MgSO 4 ), magnesium sulfite (MgSO 3 ), magnesium hyposulfite (MgSO 2 ), calcium sulfate (CaSO) 4 ), calcium sulfite (CaSO 3 ), calcium hyposulfite (CaSO 2 ), sodium sulfate (Na2SO 4 ), sodium sulfite (Na 2 SO 3 ), sodium hyposulfite (Na 2 SO 2 ), potassium sulfate (K 2 SO 4 ) , potassium sulfite (K 2 SO 3 ), potassium hyposulfite (K 2 SO 2 ), ferrous sulfate (FeSO 4 ), ferrous sulfite (FeSO 3 ), ferrous hyposulfite (FeSO 2 ), ferric sulfate (Fe 2 (SO 4 ) ) 3 ), ferric sulfite (MgSO 4 ), magnesium s
- step 2) the insoluble lithium compound is subjected to a hydrothermal reaction with an aqueous solution of the compound having the structure of Formula 1 at a temperature of 40 to 300° C., and the following relation (3) and (4) may be satisfied.
- the lithium sulfate aqueous solution prepared in step 2) may contain lithium ions at a concentration of 20,000 to 34,000 mg/L.
- step 3 is
- step 3-1) the purification is performed with an alkaline solvent, but the pH may be adjusted to 9 to 12.5.
- the lithium compound for recovering lithium ions may be a lithium compound for a cathode material.
- lithium ions can be recovered with high efficiency, and at the same time, energy consumption and usage of an alkali solvent for purification can be remarkably reduced, so that lithium ions can be recovered in an environmentally friendly manner.
- FIG. 1 is a view showing a method of manufacturing a lithium compound for recovering lithium ions according to a preferred embodiment of the present invention in each step.
- Figure 2a shows the lithium ion concentration of the desorbed solution (desorption solution conductivity, blue) and the mother solution according to the number of repetitions when the lithium hydroxide aqueous solution having a lithium ion concentration of about 1,000 mg/L was repeatedly concentrated through the membrane capacitive desalting process. It is a graph showing the change in lithium ion concentration (adsorption mother liquid conductivity, black).
- Figure 2b shows the number of repetitions when lithium ions are concentrated by repeatedly performing a membrane capacitive desalting process while removing a residual solution in an electrode from an aqueous lithium hydroxide solution of about 1,000 mg/L by the method according to a preferred embodiment of the present invention
- the XRD spectrum (blue) of the precipitate precipitated by reacting the molar ratio of 1 to 1 and the XRD spectrum (red) of the precipitate precipitated by reacting the aluminate (NaAlO 2 )-based precipitant with the molar ratio of Li/Al to 0.5 are respectively shown.
- Figure 4a is a precipitate generated by the hydrothermal reaction when the insoluble lithium compound Li 3 PO 4 is hydrothermalized with an Al 2 (SO 4 ) 3 aqueous solution at 80° C. for 8 hours according to a preferred embodiment of the present invention (top), hydrothermal
- the XRD spectrum for reference (bottom) is shown for the insoluble lithium compound used in the reaction (middle) and the precipitate (AlPO 4 ) that may be generated by the hydrothermal reaction of lithium phosphate and aluminum sulfate solutions. From the experimental results, it was confirmed that the precipitate produced by the hydrothermal reaction of lithium phosphate and aluminum sulfate solutions exhibited amorphous properties.
- Figure 4b shows the insoluble lithium compound LiF in the MgSO 4 aqueous solution and the solid-liquid ratio of the mass (g) of LiF to the volume (L) of the MgSO 4 aqueous solution is 100:1 according to a preferred embodiment of the present invention, and the Li/Mg molar ratio is 1
- the XRD spectrum (top) of the precipitate obtained as a result of performing a hydrothermal reaction at 80°C for 8 hours with :2 (bottom) is compared with the XRD spectrum for reference for MgF 2 (bottom).
- FIG. 5 is a diagram showing the solid-liquid ratio of the insoluble lithium compound LiF and MgSO 4 aqueous solution when the insoluble lithium compound LiF and MgSO 4 aqueous solution are hydrothermally reacted with a molar ratio of Li and Mg of 1.92:1 according to a preferred embodiment of the present invention. It is a graph showing the change in the lithium ion concentration of the lithium sulfate aqueous solution produced according to the method.
- the conventional lithium ion recovery method has disadvantages in that the recovery rate is poor, excessive energy is consumed in the recovery process, or a large amount of waste liquid is generated after recovery, thereby causing a burden on the environment.
- the present inventors in order to solve the above problems, 1) precipitating an insoluble lithium compound in a raw material solution containing lithium ions;
- a method for preparing a lithium compound with a high recovery rate was provided to solve this problem.
- A is one or more cations selected from magnesium, calcium, sodium, potassium, iron (Fe), ammonium and aluminum, y is an integer of 2 to 4, and z is 1 or 3.
- the insoluble lithium compound is reacted with the compound represented by the above general formula 1, but by hydrothermal synthesis, the reaction can be performed at a significantly lower temperature compared to the conventional chlorine roasting or calcination reaction, thereby reducing energy consumption. It is an economical method, and compared to the method of preparing an aqueous lithium sulfate solution or an aqueous lithium compound solution such as lithium chloride using a strong acid (sulfuric acid, hydrochloric acid, etc.), it should be used to recover the lithium compound for lithium ion recovery from the lithium compound aqueous solution. Since the amount of alkali solvent can be significantly reduced, it is economical and has the advantage of less problems of environmental pollution by waste liquid.
- step 1) is a step of producing an insoluble lithium compound, which is a reactant for preparing a highly concentrated lithium ion solution, in order to produce a lithium compound with a high recovery rate, and an insoluble lithium compound by reaction from a solution containing lithium ions is the precipitation step.
- step 1) may further include a pretreatment step. That is, preferably, step 1)
- MCDI membrane capacitive desalination process
- the source of the lithium-containing raw material for recovering lithium ions is preferably from at least one selected from lithium salt lake, waste liquid from the lithium compound manufacturing process, lithium secondary battery cathode material washing water, and lithium secondary battery recycling process waste liquid. It is not limited.
- the lithium ion source generally has a low concentration of lithium ions, the amount of the insoluble lithium compound precipitated by the precipitation reaction is inevitably small, which causes a problem in that the recovery rate of lithium ions is lowered. Therefore, in order to improve the recovery rate of lithium ions, it is preferable to concentrate the concentration of the lithium ions.
- the lithium ion-concentrated solution is a raw material solution, and the lithium ion concentration of the raw material solution may satisfy both the following relational expressions (1) and (2).
- the lithium ion concentration is less than 1.5 times or the lithium ion concentration of the concentrated raw material solution is less than 2000 mg/L, the lithium ion concentration of the raw material solution is low and the amount of insoluble lithium compound obtainable by the precipitation reaction is significantly reduced.
- lithium ion concentration may be preferably performed by a membrane capacity deionization process.
- the lithium ion concentration is continuously concentrated while repeatedly adsorbing and desorbing lithium ions to the electrode. In between, the operation of removing the residual solution in the electrode may be performed.
- the system potential of the membrane capacitive desalination process is kept the same as a whole, it is preferably set to 0.7 ⁇ 1.5V.
- Step 1-1) may be repeated 5 or more times. More preferably, it may be repeated 8 or more times. As the number of iterations increases, the process cost increases, but the concentration of lithium ions also increases. If it is less than 5 times, it is difficult to achieve the object of the present invention in the subsequent process because the lithium ion concentration of 2000 mg/L is not reached.
- step 1-2 An insoluble lithium compound is obtained through step 1-2), and the insoluble lithium compound may be preferably obtained by precipitating a lithium compound from the concentrated raw material solution.
- the insoluble lithium compound may be at least one selected from lithium phosphate (Li 3 PO 4 ), lithium fluoride (LiF), and lithium aluminate (LiAlO 2 ).
- step 1-2 a precipitating agent is added to the raw material solution to precipitate an insoluble lithium compound
- the equivalent ratio of the precipitating agent may be added to be 0.5-5 with respect to the lithium ion of the raw material solution.
- equivalence ratio is less than 0.5 equivalence ratio, unreacted lithium remains and a sufficient insoluble lithium compound cannot be produced, and the recovery rate may be lowered.
- a high concentration lithium concentrated solution is prepared by reacting the insoluble lithium compound with an aqueous solution containing the compound represented by Formula 1 above.
- an aqueous solution of lithium sulfate can be prepared.
- the lithium compound which is the object of the present invention, can be obtained in high recovery from the lithium sulfate aqueous solution.
- lithium sulfate is a concept of a lithium compound containing sulfur including all compounds having a partial difference in the number of oxygen and the oxidation state of sulfur, such as lithium sulfite and lithium hyposulfite, as well as lithium sulfate.
- the compound represented by Formula 1 in step 2) is magnesium sulfate (MgSO 4 ), magnesium sulfite (MgSO 3 ), magnesium hyposulfite (MgSO 2 ), calcium sulfate (CaSO) 4 ), calcium sulfite (CaSO 3 ), calcium hyposulfite (CaSO 2 ), sodium sulfate (Na2SO 4 ), sodium sulfite (Na 2 SO 3 ), sodium hyposulfite (Na 2 SO 2 ), potassium sulfate (K 2 SO 4 ) , potassium sulfite (K 2 SO 3 ), potassium hyposulfite (K 2 SO 2 ), ferrous sulfate (FeSO 4 ), ferrous sulfite (FeSO 3 ), ferrous hyposulfite (FeSO 2 ), ferric sulfate (Fe 2 (SO 4 ) ) 3 ), ferric sulfite (Fe (FeSO 4 ), ferrous
- step 2) the insoluble lithium compound is subjected to a hydrothermal reaction with an aqueous solution of the compound having the structure of Formula 1 at a temperature of 40 to 300° C., and the following relation (3) and (4) may be satisfied.
- the m unsol /V sol is called a solid-liquid ratio
- the solid-liquid ratio is less than 50 g/L
- the solid-liquid ratio exceeds 300 g/L, the lithium ion concentration of the lithium sulfate aqueous solution increases, but even if the solid-liquid ratio is increased beyond that, it does not increase due to the solubility of lithium sulfate itself. It is preferable to set L as the upper limit.
- the lithium sulfate aqueous solution prepared in step 2) may contain lithium ions at a concentration of 10,000 to 34,000 mg/L.
- concentration of lithium ions is less than 10,000 mg/L, there may be a problem of a decrease in recovery, and when it exceeds 34,000 mg/L, it is difficult to achieve the solubility of lithium sulfate.
- step 3 A lithium compound is obtained through step 3), and lithium ions can be recovered by obtaining a lithium compound in a form that can be directly used.
- a lithium compound is called a lithium compound for recovering lithium ions, and lithium carbonate or lithium hydroxide is preferable. However, it is not necessarily limited thereto.
- step 3 is
- the carbonation reaction is performed by reacting with CO 2 or Na 2 CO 3 , preferably by reacting a purified aqueous lithium sulfate solution with Na 2 CO 3 , and the hydroxylation reaction is preferably performed with Sr(OH) 2 It can be carried out by reacting.
- step 3-1) the purification is performed with an alkaline solvent, but the pH may be adjusted to 9 to 12.5. If the pH is less than 9, there may be a problem of impurities remaining, and if it exceeds 12.5, there may be problems of economical degradation and environmental load due to the use of an excessive amount of alkaline solvent.
- the lithium compound for recovering lithium ions obtained in this way may be preferably used as a material for a cathode material.
- an MCDI process was performed by preparing an aqueous lithium hydroxide solution having a lithium ion concentration of about 1,000 mg/L.
- the MCDI process was performed using Wonatech equipment (MP2), positive and negative electrodes were used, and the supply flow rate of the lithium hydroxide aqueous solution (adsorption mother liquid) during adsorption was 200 mL/min, and distilled water during desorption (desorption solution) )
- the supply flow rate was also set to 200 mL/min.
- the potentials of the MCDI system during adsorption and desorption were made the same at 1.3 V, respectively.
- Example 1 Between adsorption and desorption, the adsorption and desorption processes were performed without removing the solution remaining in the electrode while maintaining the potential after lithium ions were adsorbed to the electrode.
- the lithium ion concentration of the lithium solution which changed while the concentration process was performed 1 to 9 times, was measured as the conductivity of the adsorption mother solution and the desorption solution, and is shown in FIG. 2A below.
- Example 2 The same procedure as in Example 1, except that between adsorption and desorption, the solution remaining in the electrode is removed by an air flow method while maintaining the potential after lithium ions are adsorbed to the electrode, and the desorption solution is circulated to carry out the concentration process proceeded.
- the lithium ion concentration of the lithium solution which changed while the concentration process was performed 1 to 8 times, was measured as the conductivity of the adsorption mother solution and the desorption solution, and is shown in FIG. 2B below.
- Example 2a and 2b in the MCDI process, in the process according to Example 1 in which the residual solution in the electrode is not removed before desorption after adsorption, the number of adsorption/desorption is 8 times as the number of adsorption/desorption is increased From the above, it was confirmed that the concentration of lithium ions converges to 1,679 mg/L. On the other hand, in Example 2, it was confirmed that lithium ions were concentrated more than twice as compared to Example 1 at a concentration of 2,289 mg/L when repeated 8 times by removing the residual solution in the electrode.
- H 3 PO 4 , NaF and NaAlO 2 were prepared.
- H 3 PO 4 , NaF and NaAlO 2 are equivalent to 1/3 mole, 1 mole, and 1/2 mole, respectively, based on 1 mole of LiOH.
- the precipitation reaction was performed by varying the lithium ion concentration of the lithium raw material solution and the addition amount of the precipitating agent as shown in Table 1 below, and the recovery rate of lithium ions recovered as a precipitate was compared.
- the recovery rate was measured by Equation 1 below.
- Example 6 2176.32 H 3 PO 4 1.00 111.76 94.86
- Example 7 2176.32 H 3 PO 4 1.25 605.47 72.18
- Example 8 2176.32 H 3 PO 4 1.50 943.56 56.64
- Example 9 3313.52 H 3 PO 4 1.00 135.3 95.92
- the recovery rate of lithium ions in the precipitation reaction of insoluble lithium compounds can be improved when lithium ions of 2,000 mg/L or more are concentrated from a low-concentration lithium ion raw material solution through the MCDI process.
- Example 3 is compared with Examples 4 and 5
- Example 6 is compared with Examples 7 and 8
- Example 9 is compared with Examples 10 and 11
- 1 equivalent of the precipitating agent is preferably added, but it is preferably added in 0.9 to 1.05 equivalents, and when the additive is added more than that, the recovery rate is rather reduced.
- LiF, Li 3 PO 4 , LiAlO 2 , which are insoluble lithium compounds precipitated in step 2) were hydrothermal and reacted with an aqueous sulfur oxide solution as follows to prepare a high concentration lithium sulfate aqueous solution.
- the hydrothermal reaction was carried out for 1 to 8 hours, and as shown in Table 2 below, the sulfate, solid-liquid ratio of the insoluble lithium compound and the sulfur oxide aqueous solution (the mass (g) of the insoluble lithium compound relative to the volume (L) of the sulfur oxide aqueous solution) and lithium-
- the lithium ion concentration of the lithium sulfate aqueous solution obtained by adjusting the sulfur molar ratio was measured.
- FIG. 5 is a graph showing the lithium ion concentration of the lithium sulfate aqueous solution prepared according to Examples 12, 15 and 16 according to the solid-liquid ratio. It was found that the lithium ion concentration of the lithium sulfate aqueous solution increased as the solid-liquid ratio increased.
- titration was performed using calcium hydroxide (Ca(OH) 2 ).
- the pH was titrated to be 10 or more, and since the pH was higher than that in the case of preparing a lithium sulfate solution by the conventional sulfuric acid leaching method, titration was possible using a smaller amount of an alkali solution.
- the amount of sulfate ions can be reduced, thereby reducing the amount of Na 2 CO 3 and Sr(OH) 2 used.
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Abstract
Description
구분 | 침전 전 리튬이온 농도 (mg/L) |
침전제 | 첨가당량 | 침전 후 리튬이온 농도 (mg/L) |
회수율 (%) |
실시예 3 | 1069.34 | H3PO4 | 1.00 | 200.99 | 81.20 |
실시예 4 | 1069.34 | H3PO4 | 1.25 | 582.74 | 45.51 |
실시예 5 | 1069.34 | H3PO4 | 1.50 | 778.24 | 27.22 |
실시예 6 | 2176.32 | H3PO4 | 1.00 | 111.76 | 94.86 |
실시예 7 | 2176.32 | H3PO4 | 1.25 | 605.47 | 72.18 |
실시예 8 | 2176.32 | H3PO4 | 1.50 | 943.56 | 56.64 |
실시예 9 | 3313.52 | H3PO4 | 1.00 | 135.3 | 95.92 |
실시예 10 | 3313.52 | H3PO4 | 1.25 | 779.66 | 76.47 |
실시예 11 | 3313.52 | H3PO4 | 1.50 | 2475.66 | 25.29 |
불용성 리튬화합물 | 황산화물 수용액 (황산화물) |
Li-S 몰비 (nLi/nS) |
고액비 (g/L) |
황산리튬 수용액 리튬 농도 (mg/L) |
|
실시예 12 | LiF | MgSO4 | 1.92 | 100 | 25,542 |
실시예 13 | Li3PO4 | Al2(SO4)3 | 2.00 | 200 | 26,731 |
실시예 14 | LiAlO2 | MgSO4 | 1.92 | 200 | 7,178 |
실시예 15 | LiF | MgSO4 | 1.92 | 66 | 18,137 |
실시예 16 | LiF | MgSO4 | 1.92 | 133 | 33,883 |
Claims (13)
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US18/555,648 US20240208832A1 (en) | 2021-04-14 | 2022-04-06 | Method for producing lithium-concentrated solution with high recovery rate, and method for producing lithium compound using same |
EP22788333.7A EP4324792A1 (en) | 2021-04-14 | 2022-04-06 | Method for producing lithium-concentrated solution with high recovery rate, and method for producing lithium compound using same |
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