JP2020502365A5 - - Google Patents
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- JP2020502365A5 JP2020502365A5 JP2019532078A JP2019532078A JP2020502365A5 JP 2020502365 A5 JP2020502365 A5 JP 2020502365A5 JP 2019532078 A JP2019532078 A JP 2019532078A JP 2019532078 A JP2019532078 A JP 2019532078A JP 2020502365 A5 JP2020502365 A5 JP 2020502365A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- rare earth
- earth metal
- anion
- iso
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims 36
- 229910052761 rare earth metal Inorganic materials 0.000 claims 29
- 150000002910 rare earth metals Chemical class 0.000 claims 29
- -1 phthalazinium Chemical compound 0.000 claims 26
- 238000000034 method Methods 0.000 claims 25
- 239000000203 mixture Substances 0.000 claims 21
- 239000002608 ionic liquid Substances 0.000 claims 16
- 239000003929 acidic solution Substances 0.000 claims 14
- 150000001450 anions Chemical class 0.000 claims 14
- 125000003118 aryl group Chemical group 0.000 claims 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 8
- 239000008346 aqueous phase Substances 0.000 claims 8
- 125000005647 linker group Chemical group 0.000 claims 8
- 241000894007 species Species 0.000 claims 8
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 6
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 6
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims 5
- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical compound C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 claims 5
- 150000001768 cations Chemical class 0.000 claims 5
- GLUUGHFHXGJENI-UHFFFAOYSA-O hydron piperazine Chemical compound [H+].C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-O 0.000 claims 5
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 claims 5
- 239000000243 solution Substances 0.000 claims 5
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 claims 4
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 4
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 4
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 claims 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-O 1H-indol-1-ium Chemical compound C1=CC=C2[NH2+]C=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-O 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 claims 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 claims 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-O Thiophenium Chemical compound [SH+]1C=CC=C1 YTPLMLYBLZKORZ-UHFFFAOYSA-O 0.000 claims 4
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- ZRALSGWEFCBTJO-UHFFFAOYSA-O guanidinium Chemical compound NC(N)=[NH2+] ZRALSGWEFCBTJO-UHFFFAOYSA-O 0.000 claims 4
- ZCQWOFVYLHDMMC-UHFFFAOYSA-O hydron;1,3-oxazole Chemical compound C1=COC=[NH+]1 ZCQWOFVYLHDMMC-UHFFFAOYSA-O 0.000 claims 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-O hydron;pyrimidine Chemical compound C1=CN=C[NH+]=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-O 0.000 claims 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-O hydron;quinoline Chemical compound [NH+]1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-O 0.000 claims 4
- LPAGFVYQRIESJQ-UHFFFAOYSA-N indoline Chemical compound C1=CC=C2NCCC2=C1 LPAGFVYQRIESJQ-UHFFFAOYSA-N 0.000 claims 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-O isoquinolin-2-ium Chemical compound C1=[NH+]C=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-O 0.000 claims 4
- 125000000468 ketone group Chemical group 0.000 claims 4
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 claims 4
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 claims 4
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 claims 4
- XSCHRSMBECNVNS-UHFFFAOYSA-O quinoxalin-1-ium Chemical compound [NH+]1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-O 0.000 claims 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims 4
- 125000001425 triazolyl group Chemical group 0.000 claims 4
- 125000005500 uronium group Chemical group 0.000 claims 4
- SBYHFKPVCBCYGV-UHFFFAOYSA-O 1-azoniabicyclo[2.2.2]octane Chemical compound C1CC2CC[NH+]1CC2 SBYHFKPVCBCYGV-UHFFFAOYSA-O 0.000 claims 3
- 229910019142 PO4 Inorganic materials 0.000 claims 3
- CYUBECYEVLLYPK-UHFFFAOYSA-N [O+]=1BC=CC=1 Chemical compound [O+]=1BC=CC=1 CYUBECYEVLLYPK-UHFFFAOYSA-N 0.000 claims 3
- 125000004122 cyclic group Chemical group 0.000 claims 3
- 150000004820 halides Chemical class 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 229910052751 metal Inorganic materials 0.000 claims 3
- 239000002184 metal Substances 0.000 claims 3
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims 3
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims 3
- 235000021317 phosphate Nutrition 0.000 claims 3
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims 3
- 125000003831 tetrazolyl group Chemical group 0.000 claims 3
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims 3
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- FTTATHOUSOIFOQ-UHFFFAOYSA-N 1,2,3,4,6,7,8,8a-octahydropyrrolo[1,2-a]pyrazine Chemical compound C1NCCN2CCCC21 FTTATHOUSOIFOQ-UHFFFAOYSA-N 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 229910002651 NO3 Inorganic materials 0.000 claims 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims 2
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims 2
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 claims 2
- HFKJQIJFRMRSKM-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 HFKJQIJFRMRSKM-UHFFFAOYSA-N 0.000 claims 2
- 230000002378 acidificating effect Effects 0.000 claims 2
- 150000001642 boronic acid derivatives Chemical class 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims 2
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 claims 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 229910014265 BrCl Inorganic materials 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- SBUKLPSBNFWJCU-UHFFFAOYSA-N ClIBr Chemical compound ClIBr SBUKLPSBNFWJCU-UHFFFAOYSA-N 0.000 claims 1
- 229910052692 Dysprosium Inorganic materials 0.000 claims 1
- 229910052693 Europium Inorganic materials 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- 229910052779 Neodymium Inorganic materials 0.000 claims 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 241000705989 Tetrax Species 0.000 claims 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-N Thiophosphoric acid Chemical class OP(O)(S)=O RYYWUUFWQRZTIU-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 1
- 150000001413 amino acids Chemical class 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- CODNYICXDISAEA-UHFFFAOYSA-N bromine monochloride Chemical compound BrCl CODNYICXDISAEA-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 150000007942 carboxylates Chemical class 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- URSLCTBXQMKCFE-UHFFFAOYSA-N dihydrogenborate Chemical compound OB(O)[O-] URSLCTBXQMKCFE-UHFFFAOYSA-N 0.000 claims 1
- NJDNXYGOVLYJHP-UHFFFAOYSA-L disodium;2-(3-oxido-6-oxoxanthen-9-yl)benzoate Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=CC(=O)C=C2OC2=CC([O-])=CC=C21 NJDNXYGOVLYJHP-UHFFFAOYSA-L 0.000 claims 1
- KBQHZAAAGSGFKK-UHFFFAOYSA-N dysprosium atom Chemical compound [Dy] KBQHZAAAGSGFKK-UHFFFAOYSA-N 0.000 claims 1
- 238000004070 electrodeposition Methods 0.000 claims 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 claims 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000004679 hydroxides Chemical class 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 125000001518 isoselenocyanato group Chemical group *N=C=[Se] 0.000 claims 1
- 229910052746 lanthanum Inorganic materials 0.000 claims 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims 1
- 238000002386 leaching Methods 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 claims 1
- 229910017604 nitric acid Inorganic materials 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 238000001556 precipitation Methods 0.000 claims 1
- 125000002577 pseudohalo group Chemical group 0.000 claims 1
- WRHZVMBBRYBTKZ-UHFFFAOYSA-N pyrrole-2-carboxylic acid Chemical class OC(=O)C1=CC=CN1 WRHZVMBBRYBTKZ-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims 1
- 150000003871 sulfonates Chemical class 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims 1
- GWIKYPMLNBTJHR-UHFFFAOYSA-M thiosulfonate group Chemical group S(=S)(=O)[O-] GWIKYPMLNBTJHR-UHFFFAOYSA-M 0.000 claims 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 claims 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims 1
- 239000002699 waste material Substances 0.000 claims 1
- 239000012991 xanthate Substances 0.000 claims 1
- 0 CC(C)CC(N(*)*)=O Chemical compound CC(C)CC(N(*)*)=O 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1621523.8 | 2016-12-16 | ||
| GB1621523.8A GB2560871B (en) | 2016-12-16 | 2016-12-16 | Separation of rare earth matals |
| PCT/GB2017/053754 WO2018109483A1 (en) | 2016-12-16 | 2017-12-14 | Separation of rare earth metals |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020502365A JP2020502365A (ja) | 2020-01-23 |
| JP2020502365A5 true JP2020502365A5 (enExample) | 2021-03-18 |
| JP7141722B2 JP7141722B2 (ja) | 2022-09-26 |
Family
ID=58284646
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019532078A Active JP7141722B2 (ja) | 2016-12-16 | 2017-12-14 | 希土類金属の分離 |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US11396684B2 (enExample) |
| EP (1) | EP3555325B1 (enExample) |
| JP (1) | JP7141722B2 (enExample) |
| KR (1) | KR102591939B1 (enExample) |
| CN (1) | CN110300810B (enExample) |
| AR (1) | AR110383A1 (enExample) |
| AU (1) | AU2017374789B2 (enExample) |
| BR (1) | BR112019012324B1 (enExample) |
| CA (1) | CA3047051A1 (enExample) |
| CL (1) | CL2019001644A1 (enExample) |
| EA (1) | EA201991422A1 (enExample) |
| GB (1) | GB2560871B (enExample) |
| IL (1) | IL267366B2 (enExample) |
| MA (1) | MA50591A (enExample) |
| MX (1) | MX2019007042A (enExample) |
| MY (1) | MY195866A (enExample) |
| PH (1) | PH12019501379A1 (enExample) |
| PL (1) | PL3555325T3 (enExample) |
| TW (1) | TWI758375B (enExample) |
| WO (1) | WO2018109483A1 (enExample) |
| ZA (1) | ZA201903919B (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10938329B2 (en) | 2018-03-22 | 2021-03-02 | University Of Notre Dame Du Lac | Electricity generation from low grade waste heat |
| GB2607851A (en) | 2018-06-15 | 2022-12-21 | Seren Tech Limited | Rare earth metal oxide preparation |
| GB2574662B (en) * | 2018-06-15 | 2023-03-01 | Seren Tech Limited | Ionic Liquid Preparation |
| GB2578565B (en) * | 2018-06-15 | 2023-09-06 | Seren Tech Limited | Enhanced separation of rare earth metals |
| GB2607551A (en) | 2018-06-15 | 2022-12-14 | Seren Tech Limited | Countercurrent rare earth separation process |
| CN114075626B (zh) * | 2020-08-20 | 2024-01-02 | 厦门稀土材料研究所 | 一种利用水热法溶萃一体化回收稀土永磁废料中稀土金属的方法 |
| CN111961071B (zh) * | 2020-08-24 | 2023-06-02 | 江西理工大学 | 一种有机无机杂化稀土双钙钛矿化合物、制备方法及其应用 |
| CZ309827B6 (cs) * | 2020-11-13 | 2023-11-15 | Ústav organické chemie a biochemie AV ČR, v. v. i. | Použití sloučenin na bázi cyklenu pro separaci prvků vzácných zemin a způsob této separace |
| CN112280981B (zh) * | 2020-11-23 | 2021-11-26 | 中国科学院过程工程研究所 | 一种稀土高效除铝用的离子液体萃取剂及其制备方法 |
| CN112725622B (zh) * | 2020-12-02 | 2022-09-09 | 北京工业大学 | 一种两步酸浸梯次分离回收废铈基稀土抛光粉中稀土的方法 |
| JP7001861B1 (ja) | 2021-03-31 | 2022-01-20 | 第一工業製薬株式会社 | フッ素系イオン性液体およびその製造方法 |
| CN113249598B (zh) * | 2021-05-18 | 2022-07-29 | 江西理工大学 | 一种从稀土料液中络合分离除铝的方法 |
| CN113292498B (zh) * | 2021-06-16 | 2022-11-25 | 浙江工业大学 | 3-过氧苯甲酸-1-甲基咪唑氯盐及其制备和应用 |
| CN116969892A (zh) * | 2022-04-21 | 2023-10-31 | 厦门稀土材料研究所 | 一种功能离子液体及其制备方法和应用 |
| CN115992317B (zh) * | 2022-11-30 | 2024-06-18 | 核工业北京化工冶金研究院 | 一种从含稀土铀铍的硫酸浸出液中分离稀土铀铍的方法 |
| EP4484377A1 (en) * | 2023-06-26 | 2025-01-01 | ETH Zurich | An efficient separation process for rare earth element compounds and novel rare earth element complexes used therefor |
| WO2025019047A1 (en) * | 2023-07-14 | 2025-01-23 | Gillespie Andrew Peter | Continuous ion exchange processes for separating rare earth elements |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4016237A (en) | 1975-09-08 | 1977-04-05 | The United States Of America As Represented By The United States Energy Research And Development Administration | Process for separation of the rare earths by solvent extraction |
| WO2007071028A1 (en) | 2005-12-23 | 2007-06-28 | St. Mary's University | Compounds, complexes and uses thereof |
| EP2114969B1 (en) | 2007-01-31 | 2016-06-29 | Sigma Aldrich Co. LLC | High stability polyionic liquid salts |
| GB0905894D0 (en) * | 2009-04-06 | 2009-05-20 | Univ Belfast | Ionic liquids solvents for metals and metal compounds |
| GB2547364B8 (en) * | 2010-10-05 | 2017-11-29 | The Queen's Univ Of Belfast | Process for removing metals from hydrocarbons |
| WO2012079129A1 (en) * | 2010-12-17 | 2012-06-21 | University Of South Australia | Extraction of gold |
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| CN103451427B (zh) | 2013-09-24 | 2014-11-26 | 兰州大学 | 一种重稀土与轻稀土金属的分离方法及分离萃取剂 |
| WO2015106324A1 (en) * | 2014-01-17 | 2015-07-23 | Katholieke Universiteit Leuven Ku Leuven Research & Development | Process for extraction and separation of rare earths by split-anion extraction with ionic liquids |
| CN103961978B (zh) | 2014-05-15 | 2016-02-24 | 中国科学院过程工程研究所 | 一种含叔胺基和腈基吡啶类功能化离子液体捕集二氧化硫的方法 |
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| CN105219979B (zh) * | 2015-10-14 | 2017-04-26 | 北京科技大学 | 一种分离La、Ce、Pr、Nd混合稀土离子的萃取柱色层法 |
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