CA1052585A - Extraction du zinc par echange d'ions en phase liquide - Google Patents

Extraction du zinc par echange d'ions en phase liquide

Info

Publication number: CA1052585A
Authority: CA; Canada
Prior art keywords: hydroxyquinoline; hydroxy; chloro; substituted; weight
Prior art date: 1974-03-04
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.): Expired

Application number

CA218,131A

Other languages

English (en)

Other versions

CA218131S (en

Inventor

Robert B. Sudderth

Wayne H. Jensen

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

General Mills Chemicals Inc

Original Assignee

General Mills Chemicals Inc

Priority date (The priority date 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 date listed.)

1974-03-04

Filing date

1975-01-17

Publication date

1979-04-17

1975-01-17 Application filed by General Mills Chemicals Inc filed Critical General Mills Chemicals Inc

1979-04-17 Application granted granted Critical

1979-04-17 Publication of CA1052585A publication Critical patent/CA1052585A/fr

Status Expired legal-status Critical Current

Links

239000011701 zinc Substances 0.000 title description 53
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 title description 30
229910052725 zinc Inorganic materials 0.000 title description 30
238000000605 extraction Methods 0.000 title description 21
239000007788 liquid Substances 0.000 title description 3
238000005342 ion exchange Methods 0.000 title 1
239000000243 solution Substances 0.000 description 33
239000003153 chemical reaction reagent Substances 0.000 description 23
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 22
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
-1 phenolic oximes Chemical class 0.000 description 21
239000000047 product Substances 0.000 description 17
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
229910001868 water Inorganic materials 0.000 description 16
150000002923 oximes Chemical class 0.000 description 15
150000004325 8-hydroxyquinolines Chemical class 0.000 description 13
150000001875 compounds Chemical class 0.000 description 13
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
239000002253 acid Substances 0.000 description 12
239000000203 mixture Substances 0.000 description 12
239000002904 solvent Substances 0.000 description 12
125000004432 carbon atom Chemical group C* 0.000 description 11
239000005725 8-Hydroxyquinoline Substances 0.000 description 10
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 10
229960003540 oxyquinoline Drugs 0.000 description 10
239000012074 organic phase Substances 0.000 description 9
DINPBTCLBJIABS-UHFFFAOYSA-N 7-dodec-1-enylquinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(C=CCCCCCCCCCC)=CC=C21 DINPBTCLBJIABS-UHFFFAOYSA-N 0.000 description 8
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
125000000217 alkyl group Chemical group 0.000 description 8
239000007864 aqueous solution Substances 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
239000003350 kerosene Substances 0.000 description 7
238000000034 method Methods 0.000 description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
TWZIVEXYNWAOMT-VAWYXSNFSA-N (e)-1-chlorododec-1-ene Chemical compound CCCCCCCCCC\C=C\Cl TWZIVEXYNWAOMT-VAWYXSNFSA-N 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 6
229930195733 hydrocarbon Natural products 0.000 description 5
150000002430 hydrocarbons Chemical class 0.000 description 5
239000012071 phase Substances 0.000 description 5
229920006395 saturated elastomer Polymers 0.000 description 5
125000001424 substituent group Chemical group 0.000 description 5
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 4
UEQAYHVRGVWMRI-UHFFFAOYSA-N 5-chloro-7-dodec-1-enylquinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(C=CCCCCCCCCCC)=CC(Cl)=C21 UEQAYHVRGVWMRI-UHFFFAOYSA-N 0.000 description 4
239000004215 Carbon black (E152) Substances 0.000 description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
125000001931 aliphatic group Chemical group 0.000 description 4
238000004458 analytical method Methods 0.000 description 4
239000012043 crude product Substances 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000002244 precipitate Substances 0.000 description 4
150000003248 quinolines Chemical class 0.000 description 4
238000003756 stirring Methods 0.000 description 4
BZJTUOGZUKFLQT-UHFFFAOYSA-N 1,3,5,7-tetramethylcyclooctane Chemical group CC1CC(C)CC(C)CC(C)C1 BZJTUOGZUKFLQT-UHFFFAOYSA-N 0.000 description 3
ABVDSXUHJIXQGQ-UHFFFAOYSA-N 5-chloro-7-dodecylquinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(CCCCCCCCCCCC)=CC(Cl)=C21 ABVDSXUHJIXQGQ-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical class [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
238000009835 boiling Methods 0.000 description 3
238000005660 chlorination reaction Methods 0.000 description 3
CTQMJYWDVABFRZ-UHFFFAOYSA-N cloxiquine Chemical compound C1=CN=C2C(O)=CC=C(Cl)C2=C1 CTQMJYWDVABFRZ-UHFFFAOYSA-N 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical group 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
238000005984 hydrogenation reaction Methods 0.000 description 3
229910052943 magnesium sulfate Inorganic materials 0.000 description 3
239000000463 material Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
DNYZBFWKVMKMRM-UHFFFAOYSA-N n-benzhydrylidenehydroxylamine Chemical compound C=1C=CC=CC=1C(=NO)C1=CC=CC=C1 DNYZBFWKVMKMRM-UHFFFAOYSA-N 0.000 description 3
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
238000010992 reflux Methods 0.000 description 3
239000007787 solid Substances 0.000 description 3
RKAMCQVGHFRILV-UHFFFAOYSA-N 1-chlorononane Chemical compound CCCCCCCCCCl RKAMCQVGHFRILV-UHFFFAOYSA-N 0.000 description 2
DRHABPMHZRIRAH-UHFFFAOYSA-N 2,4,4,6,6-pentamethylhept-2-ene Chemical group CC(C)=CC(C)(C)CC(C)(C)C DRHABPMHZRIRAH-UHFFFAOYSA-N 0.000 description 2
NBYLBWHHTUWMER-UHFFFAOYSA-N 2-Methylquinolin-8-ol Chemical compound C1=CC=C(O)C2=NC(C)=CC=C21 NBYLBWHHTUWMER-UHFFFAOYSA-N 0.000 description 2
NWSIFTLPLKCTSX-UHFFFAOYSA-N 4-chloro-2-nitrophenol Chemical compound OC1=CC=C(Cl)C=C1[N+]([O-])=O NWSIFTLPLKCTSX-UHFFFAOYSA-N 0.000 description 2
OHYRIHZDJVDRGA-UHFFFAOYSA-N 5-bromo-7-dodecylquinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(CCCCCCCCCCCC)=CC(Br)=C21 OHYRIHZDJVDRGA-UHFFFAOYSA-N 0.000 description 2
CVICEEPAFUYBJG-UHFFFAOYSA-N 5-chloro-2,2-difluoro-1,3-benzodioxole Chemical group C1=C(Cl)C=C2OC(F)(F)OC2=C1 CVICEEPAFUYBJG-UHFFFAOYSA-N 0.000 description 2
FYMIZJXAXKUKNO-UHFFFAOYSA-N 5-chloro-7-dodec-1-enyl-3-methylquinolin-8-ol Chemical compound C1=C(C)C=NC2=C(O)C(C=CCCCCCCCCCC)=CC(Cl)=C21 FYMIZJXAXKUKNO-UHFFFAOYSA-N 0.000 description 2
VVGBHDHVFLURBA-UHFFFAOYSA-N 5-chloro-7-dodecyl-4-methylquinolin-8-ol Chemical compound CC1=CC=NC2=C(O)C(CCCCCCCCCCCC)=CC(Cl)=C21 VVGBHDHVFLURBA-UHFFFAOYSA-N 0.000 description 2
VOHHCUUIBNXCNP-UHFFFAOYSA-N 7-(5,5,7,7-tetramethyloct-1-en-3-yl)quinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(C(C=C)CC(C)(C)CC(C)(C)C)=CC=C21 VOHHCUUIBNXCNP-UHFFFAOYSA-N 0.000 description 2
WBVDIAQTOIUOSW-UHFFFAOYSA-N 7-dodecylquinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(CCCCCCCCCCCC)=CC=C21 WBVDIAQTOIUOSW-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
239000003513 alkali Substances 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
229940111121 antirheumatic drug quinolines Drugs 0.000 description 2
125000001246 bromo group Chemical group Br* 0.000 description 2
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 2
229940000425 combination drug Drugs 0.000 description 2
239000011790 ferrous sulphate Substances 0.000 description 2
235000003891 ferrous sulphate Nutrition 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 2
229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
238000011068 loading method Methods 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
239000003921 oil Substances 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
235000011149 sulphuric acid Nutrition 0.000 description 2
QAOGXSMVDWPUTB-UHFFFAOYSA-N (2-nonylphenyl)-phenylmethanone Chemical compound CCCCCCCCCC1=CC=CC=C1C(=O)C1=CC=CC=C1 QAOGXSMVDWPUTB-UHFFFAOYSA-N 0.000 description 1
DVOYYVNTAWFQAV-UHFFFAOYSA-N 1-chloro-5,5,7,7-tetramethyloct-2-ene Chemical compound CC(C)(C)CC(C)(C)CC=CCCl DVOYYVNTAWFQAV-UHFFFAOYSA-N 0.000 description 1
MLRVZFYXUZQSRU-UHFFFAOYSA-N 1-chlorohexane Chemical compound CCCCCCCl MLRVZFYXUZQSRU-UHFFFAOYSA-N 0.000 description 1
FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
FGTCYTZEIKWZRE-UHFFFAOYSA-N 2-chloro-6-(N-hydroxy-C-phenylcarbonimidoyl)-4-nonylphenol Chemical compound CCCCCCCCCC1=CC(Cl)=C(O)C(C(=NO)C=2C=CC=CC=2)=C1 FGTCYTZEIKWZRE-UHFFFAOYSA-N 0.000 description 1
SKWGLHQXFORVJD-UHFFFAOYSA-N 5-bromo-7-dodecyl-2-methylquinolin-8-ol Chemical compound C1=CC(C)=NC2=C(O)C(CCCCCCCCCCCC)=CC(Br)=C21 SKWGLHQXFORVJD-UHFFFAOYSA-N 0.000 description 1
UFEVEKUEVOSRJT-UHFFFAOYSA-N 5-chloro-3-methylquinolin-8-ol Chemical compound OC1=CC=C(Cl)C2=CC(C)=CN=C21 UFEVEKUEVOSRJT-UHFFFAOYSA-N 0.000 description 1
VKECXRPCUSXANC-UHFFFAOYSA-N 5-chloro-7-(10-methylundec-1-enyl)quinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(C=CCCCCCCCC(C)C)=CC(Cl)=C21 VKECXRPCUSXANC-UHFFFAOYSA-N 0.000 description 1
WRNNQLXYLRGUTA-UHFFFAOYSA-N 5-chloro-7-(10-methylundec-1-enyl)quinolin-8-ol 2-methylprop-1-ene Chemical compound CC(C)=C.CC(C)=C.CC(C)=C.C1=CC=NC2=C(O)C(C=CCCCCCCCC(C)C)=CC(Cl)=C21 WRNNQLXYLRGUTA-UHFFFAOYSA-N 0.000 description 1
VPTDIGMOADCHGA-UHFFFAOYSA-N 5-chloro-7-dodecyl-2-methylquinolin-8-ol Chemical compound C1=CC(C)=NC2=C(O)C(CCCCCCCCCCCC)=CC(Cl)=C21 VPTDIGMOADCHGA-UHFFFAOYSA-N 0.000 description 1
OEUICWRAHIHDJZ-UHFFFAOYSA-N 5-chloro-7-oct-1-enylquinolin-8-ol Chemical compound C1=CC=NC2=C(O)C(C=CCCCCCC)=CC(Cl)=C21 OEUICWRAHIHDJZ-UHFFFAOYSA-N 0.000 description 1
YSBJUGXCWIEWLD-UHFFFAOYSA-N 7-dodec-1-enyl-2-methylquinolin-8-ol Chemical compound C1=CC(C)=NC2=C(O)C(C=CCCCCCCCCCC)=CC=C21 YSBJUGXCWIEWLD-UHFFFAOYSA-N 0.000 description 1
BHWWGVDLAQGFOR-UHFFFAOYSA-N 7-dodecyl-2-methylquinolin-8-ol Chemical compound C1=CC(C)=NC2=C(O)C(CCCCCCCCCCCC)=CC=C21 BHWWGVDLAQGFOR-UHFFFAOYSA-N 0.000 description 1
101000856746 Bos taurus Cytochrome c oxidase subunit 7A1, mitochondrial Proteins 0.000 description 1
BGWNEGDRVYDLBK-UHFFFAOYSA-N CC=C.CC=C.CC=C.CC=C.C1=CC=NC2=C(O)C(C=CCCCCCCCC(C)C)=CC(Cl)=C21 Chemical compound CC=C.CC=C.CC=C.CC=C.C1=CC=NC2=C(O)C(C=CCCCCCCCC(C)C)=CC(Cl)=C21 BGWNEGDRVYDLBK-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
102100025597 Caspase-4 Human genes 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
101100273284 Homo sapiens CASP4 gene Proteins 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
YXAJNVUUZOLUSA-UHFFFAOYSA-N acetohydrazide;pyridin-1-ium;chloride Chemical compound [Cl-].CC(=O)NN.C1=CC=[NH+]C=C1 YXAJNVUUZOLUSA-UHFFFAOYSA-N 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000003493 decenyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
239000010931 gold Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000010410 layer Substances 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
YFBPWLXQILLTFR-UHFFFAOYSA-N n-[(2-nonylphenyl)-phenylmethylidene]hydroxylamine Chemical compound CCCCCCCCCC1=CC=CC=C1C(=NO)C1=CC=CC=C1 YFBPWLXQILLTFR-UHFFFAOYSA-N 0.000 description 1
125000005064 octadecenyl group Chemical group C(=CCCCCCCCCCCCCCCCC)* 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
239000012044 organic layer Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229920000137 polyphosphoric acid Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
FNXKBSAUKFCXIK-UHFFFAOYSA-M sodium;hydrogen carbonate;8-hydroxy-7-iodoquinoline-5-sulfonic acid Chemical class [Na+].OC([O-])=O.C1=CN=C2C(O)=C(I)C=C(S(O)(=O)=O)C2=C1 FNXKBSAUKFCXIK-UHFFFAOYSA-M 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000011269 tar Substances 0.000 description 1
229950011008 tetrachloroethylene Drugs 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G9/00—Compounds of zinc
- C01G9/003—Preparation involving a liquid-liquid extraction, an adsorption or an ion-exchange
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/26—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
- C22B3/36—Heterocyclic compounds
- C22B3/362—Heterocyclic compounds of a single type
- C22B3/364—Quinoline
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
- C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
- C22B3/26—Treatment or purification of solutions, e.g. obtained by leaching by liquid-liquid extraction using organic compounds
- C22B3/40—Mixtures
- C22B3/406—Mixtures at least one compound thereof being a heterocyclic compound
- 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

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Organic Chemistry (AREA)
Materials Engineering (AREA)
Geology (AREA)
Geochemistry & Mineralogy (AREA)
Manufacturing & Machinery (AREA)
General Life Sciences & Earth Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Mechanical Engineering (AREA)
Metallurgy (AREA)
Environmental & Geological Engineering (AREA)
Inorganic Chemistry (AREA)
Quinoline Compounds (AREA)
Extraction Or Liquid Replacement (AREA)
Manufacture And Refinement Of Metals (AREA)

CA218,131A 1974-03-04 1975-01-17 Extraction du zinc par echange d'ions en phase liquide Expired CA1052585A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US44763074A	1974-03-04	1974-03-04

Publications (1)

Publication Number	Publication Date
CA1052585A true CA1052585A (fr)	1979-04-17

Family

ID=23777116

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA218,131A Expired CA1052585A (fr)	1974-03-04	1975-01-17	Extraction du zinc par echange d'ions en phase liquide

Country Status (6)

Country	Link
JP (1)	JPS50120421A (fr)
AU (1)	AU7777875A (fr)
CA (1)	CA1052585A (fr)
GB (1)	GB1499139A (fr)
ZA (1)	ZA75411B (fr)
ZM (1)	ZM1675A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE408268B (sv) *	1977-07-11	1979-06-05	Berol Kemi Ab	Sett att selektivt extrahera metalljoner ur en vattenlosning samt extraktionsreagens for detta
LU83449A1 (fr) *	1981-06-22	1983-04-06	Metallurgie Hoboken	Procede pour separer du germanium d'une solution aqueuse a l'aide d'un alpha-hydroxyoxime
AT388570B (de) *	1986-11-07	1989-07-25	Bleiberger Bergwerks Union Ag	Extraktionsmittel sowie verfahren zur aufarbeitung von ge-haeltigen waesserigen loesungen durch fluessig/fluessigextraktion
DE3719437A1 (de) *	1987-06-11	1988-12-22	Hoechst Ag	Verfahren zur gewinnung von gallium aus basisch waessrigen natriumaluminatloesungen durch fluessig-fluessigextraktion

1975
- 1975-01-17 CA CA218,131A patent/CA1052585A/fr not_active Expired
- 1975-01-21 ZA ZA00750411A patent/ZA75411B/xx unknown
- 1975-01-31 AU AU77778/75A patent/AU7777875A/en not_active Expired
- 1975-02-10 ZM ZM16/75A patent/ZM1675A1/xx unknown
- 1975-02-26 JP JP50022989A patent/JPS50120421A/ja active Pending
- 1975-03-04 GB GB8932/75A patent/GB1499139A/en not_active Expired

Also Published As

Publication number	Publication date
GB1499139A (en)	1978-01-25
ZA75411B (en)	1976-01-28
JPS50120421A (fr)	1975-09-20
ZM1675A1 (en)	1975-12-22
AU7777875A (en)	1976-08-05

Publication	Publication Date	Title
US4923686A (en)	1990-05-08	Process for the extraction of metal values
US4051223A (en)	1977-09-27	Process for the recovery of magnesium
US4029704A (en)	1977-06-14	Oximes
US4065455A (en)	1977-12-27	5-Halogen-substituted 7 alkyl and 7-alkenyl 8-hydroxyquinolines
US4039612A (en)	1977-08-02	Process for extracting cobalt, copper or zinc values using a 1-alkyl substituted benzimidazole
CA1052585A (fr)	1979-04-17	Extraction du zinc par echange d'ions en phase liquide
US3592775A (en)	1971-07-13	Compositions containing phenolic oximes and certain alpha-hydroxy aliphatic oximes
AU601243B2 (en)	1990-09-06	Gallium complexes and solvent extraction of gallium
US3939203A (en)	1976-02-17	Certain substituted 2-hydroxybenzophenoximes and the process of extracting copper therewith
US4581220A (en)	1986-04-08	Process for the extraction of metal values and novel metal extractants
CA1337243C (fr)	1995-10-10	Procede de recuperation des metaux d'une solution aqueuse utilisant certains imidazoles
US3992507A (en)	1976-11-16	Halidation of manganiferous ore to obtain metal values and recovery and recycle of halide values
US4066652A (en)	1978-01-03	Substituted 8-hydroxyquinolines and process for the preparation thereof
US3464784A (en)	1969-09-02	Extraction of tetravalent vanadium values from their aqueous solutions using hydroxamic acids
CA1252097A (fr)	1989-04-04	Procede d'extraction de metaux utiles grace a des composes cyclaniques renfermant deux atomes d'azote; produits d'extraction de metaux
US4761484A (en)	1988-08-02	2-phenyl-4-acyl-(3H)-pyrazol-3-ones
US3449066A (en)	1969-06-10	Recovery of molybdenum values from aqueous solutions using alpha-hydroxy oximes
US4576815A (en)	1986-03-18	Process for the extraction of metal values and novel metal extractants
US4739054A (en)	1988-04-19	Triazolopyrimidine extractants
US4939299A (en)	1990-07-03	Succinyl dihydroxamic acids
US3954936A (en)	1976-05-04	O-nitrosophenols as extractants for metal values
US4020081A (en)	1977-04-26	Certain benzoxazoles and the use thereof as metal extractants
CA2355853A1 (fr)	2000-07-06	Procede permettant d'extraire des anions
US4943646A (en)	1990-07-24	Gallium complexes and solvent extraction of gallium
CA2161180A1 (fr)	1996-04-27	Extraction d'acides et de sels metalliques de solutions aqueuses a l'aide de dodecylphosphonate de diethyle