SE447066B - Forfarande for flotation av oxidiska mineral samt medel - Google Patents
Forfarande for flotation av oxidiska mineral samt medelInfo
- Publication number
- SE447066B SE447066B SE8103099A SE8103099A SE447066B SE 447066 B SE447066 B SE 447066B SE 8103099 A SE8103099 A SE 8103099A SE 8103099 A SE8103099 A SE 8103099A SE 447066 B SE447066 B SE 447066B
- Authority
- SE
- Sweden
- Prior art keywords
- group
- acid
- flotation
- carbon atoms
- koh
- Prior art date
Links
- 238000005188 flotation Methods 0.000 title claims description 36
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims description 15
- 239000011707 mineral Substances 0.000 title claims description 15
- 238000000034 method Methods 0.000 title claims description 14
- 239000003795 chemical substances by application Substances 0.000 title claims description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 54
- 150000001875 compounds Chemical class 0.000 claims description 34
- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 20
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 19
- 239000000194 fatty acid Substances 0.000 claims description 19
- 229930195729 fatty acid Natural products 0.000 claims description 19
- 125000002947 alkylene group Chemical group 0.000 claims description 17
- 150000004665 fatty acids Chemical class 0.000 claims description 16
- 239000007788 liquid Substances 0.000 claims description 15
- 239000011541 reaction mixture Substances 0.000 claims description 14
- 125000001931 aliphatic group Chemical group 0.000 claims description 10
- 230000032050 esterification Effects 0.000 claims description 10
- 238000005886 esterification reaction Methods 0.000 claims description 10
- -1 ethyleneoxy group Chemical group 0.000 claims description 8
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
- 238000002474 experimental method Methods 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 125000002252 acyl group Chemical group 0.000 claims description 6
- 238000010586 diagram Methods 0.000 claims description 6
- 125000005529 alkyleneoxy group Chemical group 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 239000003760 tallow Substances 0.000 claims description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 22
- 239000003153 chemical reaction reagent Substances 0.000 description 15
- 229910052586 apatite Inorganic materials 0.000 description 14
- VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 14
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 9
- 239000002699 waste material Substances 0.000 description 8
- 150000008064 anhydrides Chemical class 0.000 description 7
- 239000000295 fuel oil Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000001143 conditioned effect Effects 0.000 description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 description 6
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 5
- 235000011613 Pinus brutia Nutrition 0.000 description 5
- 241000018646 Pinus brutia Species 0.000 description 5
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 4
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 4
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 230000003213 activating effect Effects 0.000 description 4
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 4
- 150000001735 carboxylic acids Chemical class 0.000 description 4
- 150000005690 diesters Chemical class 0.000 description 4
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 230000002209 hydrophobic effect Effects 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000011976 maleic acid Substances 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 2
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 229910021532 Calcite Inorganic materials 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 2
- 229940018557 citraconic acid Drugs 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006735 deficit Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- ZTQSADJAYQOCDD-UHFFFAOYSA-N ginsenoside-Rd2 Natural products C1CC(C2(CCC3C(C)(C)C(OC4C(C(O)C(O)C(CO)O4)O)CCC3(C)C2CC2O)C)(C)C2C1C(C)(CCC=C(C)C)OC(C(C(O)C1O)O)OC1COC1OCC(O)C(O)C1O ZTQSADJAYQOCDD-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910052595 hematite Inorganic materials 0.000 description 2
- 239000011019 hematite Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910001608 iron mineral Inorganic materials 0.000 description 2
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 229960004488 linolenic acid Drugs 0.000 description 2
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229960002969 oleic acid Drugs 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- 235000019353 potassium silicate Nutrition 0.000 description 2
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 2
- 229960003656 ricinoleic acid Drugs 0.000 description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000007873 sieving Methods 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 229960004274 stearic acid Drugs 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical compound CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/02—Froth-flotation processes
- B03D1/021—Froth-flotation processes for treatment of phosphate ores
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/008—Organic compounds containing oxygen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/02—Collectors
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Environmental & Geological Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Geology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyesters Or Polycarbonates (AREA)
- Degasification And Air Bubble Elimination (AREA)
- Polyurethanes Or Polyureas (AREA)
Priority Applications (22)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8103099A SE447066B (sv) | 1981-05-18 | 1981-05-18 | Forfarande for flotation av oxidiska mineral samt medel |
| AR289405A AR231269A1 (es) | 1981-05-18 | 1982-03-14 | Nuevo acido dicarboxilico esterificado y composicion que lo comprende |
| ZA823025A ZA823025B (en) | 1981-05-18 | 1982-05-03 | Esterified dicarboxylic acid and its use |
| IL65679A IL65679A (en) | 1981-05-18 | 1982-05-04 | Monoesters of dicarboxylic acids and collector reagents containing them for use in foam flotation |
| DE8282850103T DE3266635D1 (en) | 1981-05-18 | 1982-05-06 | Esterified dicarboxylic acid and its use |
| EP82850103A EP0067137B1 (de) | 1981-05-18 | 1982-05-06 | Veresterte Dicarboxylsäuren und ihre Verwendung |
| AT82850103T ATE15886T1 (de) | 1981-05-18 | 1982-05-06 | Veresterte dicarboxylsaeuren und ihre verwendung. |
| ZW93/82A ZW9382A1 (en) | 1981-05-18 | 1982-05-10 | Esterified dicarboxylic acid and its use |
| US06/376,338 US4430238A (en) | 1981-05-18 | 1982-05-10 | Esterified dicarboxylic acid and its use |
| MA19679A MA19473A1 (fr) | 1981-05-18 | 1982-05-12 | Acide dicarboxylique esterifie et ses applications |
| JP57082296A JPS57193424A (en) | 1981-05-18 | 1982-05-13 | Esterified dicarboxylic acid and use |
| NO821632A NO157018C (no) | 1981-05-18 | 1982-05-14 | Anvendelse av forestret dikarboksylsyre som samlereagens ved skumflotasjon. |
| CA000403025A CA1200546A (en) | 1981-05-18 | 1982-05-14 | Esterified dicarboxylic acid and its use |
| BR8202830A BR8202830A (pt) | 1981-05-18 | 1982-05-17 | Processo de flotacao com espuma |
| MX192733A MX157040A (es) | 1981-05-18 | 1982-05-17 | Procedimiento de flotacion de espuma mejorado |
| FI821727A FI71722C (fi) | 1981-05-18 | 1982-05-17 | Foerestrad dikarbonsyra och dess anvaendning som samlarreagens vid flotation. |
| ES512272A ES512272A0 (es) | 1981-05-18 | 1982-05-17 | "procedimiento de flotacion de espuma". |
| IN553/CAL/82A IN159612B (de) | 1981-05-18 | 1982-05-17 | |
| AU83765/82A AU549416B2 (en) | 1981-05-18 | 1982-05-17 | Esterfied dicarboxylic acids as ore floatation collectors |
| SU823438902A SU1097182A3 (ru) | 1981-05-18 | 1982-05-17 | Способ пенной флотации |
| YU1059/82A YU43795B (en) | 1981-05-18 | 1982-05-18 | Process for foam-flotation |
| OA57691A OA07101A (fr) | 1981-05-18 | 1982-05-18 | Acide dicarboxylique estérifié de formule générale. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8103099A SE447066B (sv) | 1981-05-18 | 1981-05-18 | Forfarande for flotation av oxidiska mineral samt medel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8103099L SE8103099L (sv) | 1982-11-19 |
| SE447066B true SE447066B (sv) | 1986-10-27 |
Family
ID=20343859
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8103099A SE447066B (sv) | 1981-05-18 | 1981-05-18 | Forfarande for flotation av oxidiska mineral samt medel |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4430238A (de) |
| EP (1) | EP0067137B1 (de) |
| JP (1) | JPS57193424A (de) |
| AR (1) | AR231269A1 (de) |
| AT (1) | ATE15886T1 (de) |
| AU (1) | AU549416B2 (de) |
| BR (1) | BR8202830A (de) |
| CA (1) | CA1200546A (de) |
| DE (1) | DE3266635D1 (de) |
| ES (1) | ES512272A0 (de) |
| FI (1) | FI71722C (de) |
| IL (1) | IL65679A (de) |
| IN (1) | IN159612B (de) |
| MA (1) | MA19473A1 (de) |
| MX (1) | MX157040A (de) |
| NO (1) | NO157018C (de) |
| OA (1) | OA07101A (de) |
| SE (1) | SE447066B (de) |
| SU (1) | SU1097182A3 (de) |
| YU (1) | YU43795B (de) |
| ZA (1) | ZA823025B (de) |
| ZW (1) | ZW9382A1 (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4010911C2 (de) * | 1989-04-05 | 2000-06-08 | Berol Nobel Ab Stenungsund | Verfahren und Mittel zur Flotation eines Erdalkalimetall enthaltenden Minerals |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3641870A1 (de) * | 1986-12-08 | 1988-06-16 | Henkel Kgaa | Alkylsulfosuccinate auf der basis von propoxylierten sowie propoxylierten und ethoxylierten fettalkoholen als sammler fuer die flotation nichtsulfidischer erze |
| DE4030160A1 (de) * | 1990-09-24 | 1992-03-26 | Henkel Kgaa | Verfahren zur gewinnung von mineralien aus nichtsulfidischen erzen durch flotation |
| DE4138911A1 (de) * | 1991-11-27 | 1993-06-03 | Henkel Kgaa | Verfahren zur gewinnung von mineralien aus nichtsulfidischen erzen durch flotation |
| JP4022595B2 (ja) * | 2004-10-26 | 2007-12-19 | コニカミノルタオプト株式会社 | 撮影装置 |
| US8007754B2 (en) * | 2005-02-04 | 2011-08-30 | Mineral And Coal Technologies, Inc. | Separation of diamond from gangue minerals |
| CA3046326C (en) | 2016-12-23 | 2023-11-07 | Akzo Nobel Chemicals International B.V. | Collector composition for froth flotation of phosphate ores |
| CN113117594B (zh) * | 2021-05-26 | 2022-05-24 | 江南大学 | 一种松香基表面活性剂与二氧化硅纳米颗粒复合稳定剂及应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2302338A (en) | 1938-05-18 | 1942-11-17 | Moeller August | Froth flotation |
| US2759607A (en) | 1951-02-27 | 1956-08-21 | Union Oil Co | Flotation of hydrocarbon impurities |
| BE756244A (fr) * | 1969-09-17 | 1971-03-01 | Eastman Kodak Co | Nouveau produit photographique photosensible stabilise |
| US3779380A (en) | 1971-10-12 | 1973-12-18 | Hercules Inc | Collector composition for ore flotation |
| US3910986A (en) * | 1972-01-12 | 1975-10-07 | Halcon International Inc | Process for oxidizing beta-acyloxyethyl-toluates |
| JPS539244B2 (de) * | 1973-01-19 | 1978-04-04 | ||
| US4081363A (en) * | 1975-05-29 | 1978-03-28 | American Cyanamid Company | Mineral beneficiation by froth flotation: use of alcohol ethoxylate partial esters of polycarboxylic acids |
| CA1073563A (en) * | 1976-01-19 | 1980-03-11 | American Cyanamid Company | Process for beneficiation of non-sulfide ores |
| JPS6012622B2 (ja) * | 1977-12-27 | 1985-04-02 | 東レ株式会社 | ポリアミド系感光性樹脂印刷版用組成物 |
-
1981
- 1981-05-18 SE SE8103099A patent/SE447066B/sv not_active IP Right Cessation
-
1982
- 1982-03-14 AR AR289405A patent/AR231269A1/es active
- 1982-05-03 ZA ZA823025A patent/ZA823025B/xx unknown
- 1982-05-04 IL IL65679A patent/IL65679A/xx not_active IP Right Cessation
- 1982-05-06 EP EP82850103A patent/EP0067137B1/de not_active Expired
- 1982-05-06 DE DE8282850103T patent/DE3266635D1/de not_active Expired
- 1982-05-06 AT AT82850103T patent/ATE15886T1/de active
- 1982-05-10 US US06/376,338 patent/US4430238A/en not_active Expired - Lifetime
- 1982-05-10 ZW ZW93/82A patent/ZW9382A1/xx unknown
- 1982-05-12 MA MA19679A patent/MA19473A1/fr unknown
- 1982-05-13 JP JP57082296A patent/JPS57193424A/ja active Granted
- 1982-05-14 NO NO821632A patent/NO157018C/no not_active IP Right Cessation
- 1982-05-14 CA CA000403025A patent/CA1200546A/en not_active Expired
- 1982-05-17 MX MX192733A patent/MX157040A/es unknown
- 1982-05-17 ES ES512272A patent/ES512272A0/es active Granted
- 1982-05-17 IN IN553/CAL/82A patent/IN159612B/en unknown
- 1982-05-17 AU AU83765/82A patent/AU549416B2/en not_active Expired
- 1982-05-17 FI FI821727A patent/FI71722C/fi not_active IP Right Cessation
- 1982-05-17 SU SU823438902A patent/SU1097182A3/ru active
- 1982-05-17 BR BR8202830A patent/BR8202830A/pt not_active IP Right Cessation
- 1982-05-18 OA OA57691A patent/OA07101A/xx unknown
- 1982-05-18 YU YU1059/82A patent/YU43795B/xx unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4010911C2 (de) * | 1989-04-05 | 2000-06-08 | Berol Nobel Ab Stenungsund | Verfahren und Mittel zur Flotation eines Erdalkalimetall enthaltenden Minerals |
Also Published As
| Publication number | Publication date |
|---|---|
| NO157018B (no) | 1987-09-28 |
| AU8376582A (en) | 1982-11-25 |
| ATE15886T1 (de) | 1985-10-15 |
| ES8307709A1 (es) | 1983-08-01 |
| SU1097182A3 (ru) | 1984-06-07 |
| CA1200546A (en) | 1986-02-11 |
| FI821727A0 (fi) | 1982-05-17 |
| AR231269A1 (es) | 1984-10-31 |
| EP0067137B1 (de) | 1985-10-02 |
| EP0067137A1 (de) | 1982-12-15 |
| ES512272A0 (es) | 1983-08-01 |
| JPS57193424A (en) | 1982-11-27 |
| SE8103099L (sv) | 1982-11-19 |
| DE3266635D1 (en) | 1985-11-07 |
| YU43795B (en) | 1989-12-31 |
| FI71722B (fi) | 1986-10-31 |
| ZW9382A1 (en) | 1982-07-28 |
| MA19473A1 (fr) | 1982-12-31 |
| MX157040A (es) | 1988-10-20 |
| IL65679A (en) | 1986-03-31 |
| ZA823025B (en) | 1983-03-30 |
| IL65679A0 (en) | 1982-08-31 |
| US4430238A (en) | 1984-02-07 |
| OA07101A (fr) | 1987-01-31 |
| IN159612B (de) | 1987-05-30 |
| YU105982A (en) | 1985-03-20 |
| NO821632L (no) | 1982-11-19 |
| NO157018C (no) | 1988-01-06 |
| JPH0319217B2 (de) | 1991-03-14 |
| AU549416B2 (en) | 1986-01-23 |
| FI71722C (fi) | 1987-02-09 |
| BR8202830A (pt) | 1983-04-26 |
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