US3452867A - Treatment of sylvinite ores - Google Patents
Treatment of sylvinite ores Download PDFInfo
- Publication number
- US3452867A US3452867A US626943A US3452867DA US3452867A US 3452867 A US3452867 A US 3452867A US 626943 A US626943 A US 626943A US 3452867D A US3452867D A US 3452867DA US 3452867 A US3452867 A US 3452867A
- Authority
- US
- United States
- Prior art keywords
- copolymer
- kcl
- ore
- acrylamide
- ores
- 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.)
- Expired - Lifetime
Links
- 229920001577 copolymer Polymers 0.000 description 25
- 238000000034 method Methods 0.000 description 21
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 20
- 239000001103 potassium chloride Substances 0.000 description 18
- 235000011164 potassium chloride Nutrition 0.000 description 18
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 12
- 239000004927 clay Substances 0.000 description 11
- 235000002639 sodium chloride Nutrition 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 239000003112 inhibitor Substances 0.000 description 10
- 229910052500 inorganic mineral Inorganic materials 0.000 description 10
- 239000011707 mineral Substances 0.000 description 10
- 235000010755 mineral Nutrition 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 8
- 238000011084 recovery Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000005188 flotation Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- IHBKAGRPNRKYAO-UHFFFAOYSA-M methyl sulfate;trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium Chemical compound COS([O-])(=O)=O.CC(=C)C(=O)OCC[N+](C)(C)C IHBKAGRPNRKYAO-UHFFFAOYSA-M 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000009291 froth flotation Methods 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 238000012673 precipitation polymerization Methods 0.000 description 3
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical class N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000019257 ammonium acetate Nutrition 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 239000007853 buffer solution Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- WHRZCXAVMTUTDD-UHFFFAOYSA-N 1h-furo[2,3-d]pyrimidin-2-one Chemical compound N1C(=O)N=C2OC=CC2=C1 WHRZCXAVMTUTDD-UHFFFAOYSA-N 0.000 description 1
- OQUFOZNPBIIJTN-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylic acid;sodium Chemical compound [Na].OC(=O)CC(O)(C(O)=O)CC(O)=O OQUFOZNPBIIJTN-UHFFFAOYSA-N 0.000 description 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 241000272168 Laridae Species 0.000 description 1
- 235000006173 Larrea tridentata Nutrition 0.000 description 1
- 244000073231 Larrea tridentata Species 0.000 description 1
- 101100399296 Mus musculus Lime1 gene Proteins 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- XEXFVRMLYUDDJY-UHFFFAOYSA-N azane;hydrate;hydrochloride Chemical compound [NH4+].[NH4+].[OH-].[Cl-] XEXFVRMLYUDDJY-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M bisulphate group Chemical group S([O-])(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229960002126 creosote Drugs 0.000 description 1
- RHCJOJDSMWJGMV-UHFFFAOYSA-N diazanium acetate hydroxide Chemical compound [NH4+].[NH4+].[OH-].CC([O-])=O RHCJOJDSMWJGMV-UHFFFAOYSA-N 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- HDFXRQJQZBPDLF-UHFFFAOYSA-L disodium hydrogen carbonate Chemical compound [Na+].[Na+].OC([O-])=O.OC([O-])=O HDFXRQJQZBPDLF-UHFFFAOYSA-L 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 229960002089 ferrous chloride Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000010442 halite Substances 0.000 description 1
- NMCUIPGRVMDVDB-UHFFFAOYSA-L iron dichloride Chemical compound Cl[Fe]Cl NMCUIPGRVMDVDB-UHFFFAOYSA-L 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 description 1
- KDWVVKPUUIKFCO-UHFFFAOYSA-M methyl sulfate;prop-2-enamide;trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium Chemical compound NC(=O)C=C.COS([O-])(=O)=O.CC(=C)C(=O)OCC[N+](C)(C)C KDWVVKPUUIKFCO-UHFFFAOYSA-M 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- -1 nonylphenyl Chemical group 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 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
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/016—Macromolecular compounds
-
- 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
- B03D1/01—Organic compounds containing nitrogen
-
- 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
- B03D1/012—Organic compounds containing sulfur
-
- 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
- B03D2203/10—Potassium ores
Definitions
- the improvement comprises carrying (methoxyl polyethylene glycol of approximately 550 out the separation in the presence of an acrylamide-beta molecular weigh
- the amounts of materials Used in methacrylyloxyethyltrimethylammonium methyl sulfate these runs were per ton of the partially deslimed ore on copolymer which copolymer serves to minimize the ada dry weight basis.
- 0.5 pound coal tar creosote (Barverse effect of the clay on the mineral collector. rett No. 634) was added and the mixing continued for 5 minutes.
- amine collector distilled hydrogenated tallow amine acetate, commercially available as The present invention relates to a process of treating Armac HTD) was added and the mixing continued for sylvinite ores, and more particularly to a flotation proc- 2 minutes.
- the resulting ore pulp was then transferred to ess of recovering sylvite (KCl) from sylvinite ores.
- KCl sylvite
- KCl sylvite
- KCl sylvite
- KCl sylvite
- a flotation cell, and 0.07 pound methylisobutyl carbinol Sylvinite ores contain various amounts of KCl and added prior to floating.
- the KCl concentrate in the froth NaCl (halite). Typical of such sylvinite ores are those that formed was removed from the surface of the pulp in the Carlsbad district of New Mexico. Sylvinite ores liquor. also contain
- Example 2 used as SEPARAN NP an acrylamide-based anionic slime inhibitor available commercially 10.
- Froth flotation processes are used commercially to recover KCl from the ores by flotating the KCl from the NaCl.
- finely ground ore is mixed with a saturated solution of the soluble constituents (usually insoluble constituents such as e.g. clays are also present) of the ore and various flotation (collection) and auxiliary agents are added.
- the collection agent causes the separation of the KCl from the ore.
- the clay adsorbs a substantial amount of the mineral collector and thus seriously interferes with the separation process.
- it is conventional practice to employ a mechanical desliming step still enough clay remains to substantially hinder the separation process.
- the present invention is not limited thereto but includes any materials which interfere with the performance of the mineral collector, which interference the copolymer of the present invention lessens.
- These objectionable slime-forming materials are sometimes referred to in the art as insoluble clay-like minerals.
- the present invention is described herein for the most part with reference to a flotation process of concentrating KCl in sylvinite ores, the invention is not limited thereto. More specifically the present invention is applicable to KCl concentrating processes in general including e.g. those often referred to in the art as flotation, settling, and dissolution processes in general.
- the copolymer slime inhibitor of the present invention consists by weight thereof essentially of 99 %20% acrylamide and 1%-80% MTMMS, preferably about 97%- 50% acrylamide and 3%50% MTMMS, about 95% 60% acrylamide and %40% MTMMS being specifically preferred.
- the precipitation process broadly comprises polymerizing butanol, aqueous acetone or aqueous tertiary butanolacetone in the substantial absence of air while agitating the solution to give a copolymer product that can be isolated by filtration, the aqueous tertiary butanol and aqueous acetone being solvents for the monomers but nonsolvents for the copolymer product.
- the solvent for the monomers must be aqueous tertiary butanol, aqueous acetone or aqueous tertiary butanolacetone (i.e. mixtures of water with tertiary butanol or acetone alone or with both).
- concentrations of water in said mixtures must be 30%65%, preferably 45%- 60%, by weight of said mixtures.
- the polymerization reaction temperature must be 0 C.- 60" C., preferably 0 C.40 C.
- the polymerization may be carried out either in the presence or absence of a polymerization catalyst (initiator), but preferably a polymerization initiator will be used. Both the types and amounts of free radical initiator applicable are well known in this art. Peroxygen compounds are quite suitable, including e.g. ammonium persulfate, potassium persulfate and hydrogen peroxide. Other free radical initators include e.g. u,ot'-axo-bis-isobutyronitrile. The peroxygen initators may be used alone or in combination with activators (also well known in this art) including e.g.
- the amount of initator usually will not exceed 0.5%, preferably is 0.05%0.2%, 0.05% being specifically preferred, by weight of the combined weight of monomers.
- the precipitation polymerization is carried out in the presence of a salt dissolved in the polymerization reaction mixture.
- a salt or a buffer system comprising one or more salts in combination with another material to complete the buffer system, recovery of the copolymer product is substantially facilitated.
- salts and buffer systems include, e.g., (1) alkali metal and ammonium acetates, carbonates, bicarbonates, chlorides, phosphates, sulfates, bisulfates, borates; (2) buffer sys-- terns comprising (2.) mixtures of weak acid or weak base and their salts including (b) phthalates, citrates, borates, phosphates, acetates, ammonium hydroxide, ammonium acetate, ammonium chloride, (c) specific combinations including mixtures of boric acid-borax, citric acid-sodium acid phosphate, sodium carbonate-sodium bicarbonate, ammonium chloride-ammonium hydroxide, ammonium acetate-ammonium hydroxide; or (3) any combination of -(1), and (2).
- buffer sys--- terns comprising (2.) mixtures of weak acid or weak base and their salts including (b) phthalates, citrates, bor
- the amount of salt which may be used is about 0-.1%- 2.0% preferably about 0.2%0.7%, by weight of the reaction mixture. If the amount of salt exceeds about 2.0%, usually there is a tendency for the granules of the polymeric product to agglomerate in the polymerization reaction mixture.
- the manner of adding the salt and the point at which it is added are not critical.
- copolymer slime inhibitor in accordance with the present invention may be added in dry form to the ore being treated, it is preferred to add it as an aqueous solution in order to get faster and more complete dispersion thereof throughout the ore.
- copolymer consists by weight thereof essentially of 99%20% acrylamide and 1%80% beta methacrylyloxyethyltrimethylammonium methyl sulfate.
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62694367A | 1967-03-30 | 1967-03-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3452867A true US3452867A (en) | 1969-07-01 |
Family
ID=24512511
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US626943A Expired - Lifetime US3452867A (en) | 1967-03-30 | 1967-03-30 | Treatment of sylvinite ores |
Country Status (2)
Country | Link |
---|---|
US (1) | US3452867A (en, 2012) |
BE (1) | BE706550A (en, 2012) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3782546A (en) * | 1971-12-03 | 1974-01-01 | Calgon Corp | Cationic conditioning agents for potash flotation |
US3993712A (en) * | 1974-04-30 | 1976-11-23 | Calgon Corporation | Water-soluble vinyl-pyrrolidone block copolymers |
US4268379A (en) * | 1977-12-23 | 1981-05-19 | American Cyanamid Company | Selective flocculation for increased coal recovery by froth flotation |
US20100021370A1 (en) * | 2008-07-25 | 2010-01-28 | Devarayasamudram Ramachandran Nagaraj | Flotation Reagents and Flotation Processes Utilizing Same |
US20150314305A1 (en) * | 2012-12-20 | 2015-11-05 | Akzo Nobel Chemicals International B.V. | Polyquaternary Polymer as a Depressant in a Method for Froth Flotation of Potash Ores |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2740522A (en) * | 1953-04-07 | 1956-04-03 | American Cyanamid Co | Flotation of ores using addition polymers as depressants |
US2923408A (en) * | 1954-12-27 | 1960-02-02 | Dow Chemical Co | Flotation process |
US3023162A (en) * | 1956-04-10 | 1962-02-27 | Rohm & Haas | Dewatering aqueous suspensions with quaternized dialkylaminoalkyl acrylates or methacrylates |
US3321649A (en) * | 1964-12-28 | 1967-05-23 | Shell Oil Co | Separation of suspended solids by cationic polymeric flocculants |
-
1967
- 1967-03-30 US US626943A patent/US3452867A/en not_active Expired - Lifetime
- 1967-11-14 BE BE706550D patent/BE706550A/xx unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2740522A (en) * | 1953-04-07 | 1956-04-03 | American Cyanamid Co | Flotation of ores using addition polymers as depressants |
US2923408A (en) * | 1954-12-27 | 1960-02-02 | Dow Chemical Co | Flotation process |
US3023162A (en) * | 1956-04-10 | 1962-02-27 | Rohm & Haas | Dewatering aqueous suspensions with quaternized dialkylaminoalkyl acrylates or methacrylates |
US3321649A (en) * | 1964-12-28 | 1967-05-23 | Shell Oil Co | Separation of suspended solids by cationic polymeric flocculants |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3782546A (en) * | 1971-12-03 | 1974-01-01 | Calgon Corp | Cationic conditioning agents for potash flotation |
US3993712A (en) * | 1974-04-30 | 1976-11-23 | Calgon Corporation | Water-soluble vinyl-pyrrolidone block copolymers |
US4268379A (en) * | 1977-12-23 | 1981-05-19 | American Cyanamid Company | Selective flocculation for increased coal recovery by froth flotation |
US20100021370A1 (en) * | 2008-07-25 | 2010-01-28 | Devarayasamudram Ramachandran Nagaraj | Flotation Reagents and Flotation Processes Utilizing Same |
US8720694B2 (en) | 2008-07-25 | 2014-05-13 | Cytec Technology Corp. | Flotation reagents and flotation processes utilizing same |
US10130956B2 (en) | 2008-07-25 | 2018-11-20 | Cytec Technology Corp. | Flotation reagents and flotation processes utilizing same |
US11007538B2 (en) | 2008-07-25 | 2021-05-18 | Cytec Technology Corp. | Flotation reagents and flotation processes utilizing same |
US20150314305A1 (en) * | 2012-12-20 | 2015-11-05 | Akzo Nobel Chemicals International B.V. | Polyquaternary Polymer as a Depressant in a Method for Froth Flotation of Potash Ores |
US9486815B2 (en) * | 2012-12-20 | 2016-11-08 | Akzo Nobel Chemicals International B.V. | Polyquaternary polymer as a depressant in a method for froth flotation of potash ores |
Also Published As
Publication number | Publication date |
---|---|
BE706550A (en, 2012) | 1968-03-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3418237A (en) | Settling of non-argillaceous ore pulps and mineral suspensions by use of water-soluble acrylic polymers | |
US3782546A (en) | Cationic conditioning agents for potash flotation | |
US4119508A (en) | Method of purifying the raw brine used in alkali salt electrolysis | |
US3321649A (en) | Separation of suspended solids by cationic polymeric flocculants | |
US3452867A (en) | Treatment of sylvinite ores | |
US4060465A (en) | Method of purifying the raw brine used in alkali salt electrolysis | |
US2569672A (en) | Flotation of slimes from sylvinite ore with hydroxyethyl cellulose | |
US4141691A (en) | Use of water soluble polymers in coal flotation circuits | |
US2407651A (en) | Concentrating fluorspar by froth flotation | |
US2923408A (en) | Flotation process | |
US3240556A (en) | Process for the recovery of metal values | |
US3862028A (en) | Flotation-beneficiation of phosphate ores | |
US3891544A (en) | Process for the separate recovery of potassium chloride and sodium chloride from a solid mixture thereof | |
US3164549A (en) | Flotation separation of phosphate ores | |
US3128248A (en) | Method for the purification of brine | |
US3079331A (en) | Process of recovering coal fines | |
US3638791A (en) | Method for treatment of heavy media | |
CN117884259B (zh) | 一种多金属矿选矿分离药剂及其制备方法和应用 | |
US3479284A (en) | Separation of finely divided solids from liquid suspensions thereof | |
AU2023222824B2 (en) | High entropy collecting flotation method for low grade zinc oxide ore | |
US2968525A (en) | Potash ore treatment | |
US3985645A (en) | Scheelite flotation | |
US3207304A (en) | Method of concentrating fluorspar ores | |
US3309029A (en) | Activation of sulfide ores for froth flotation | |
US2695100A (en) | Sylvite concentration process |