US2302338A - Froth flotation - Google Patents
Froth flotation Download PDFInfo
- Publication number
- US2302338A US2302338A US273144A US27314439A US2302338A US 2302338 A US2302338 A US 2302338A US 273144 A US273144 A US 273144A US 27314439 A US27314439 A US 27314439A US 2302338 A US2302338 A US 2302338A
- Authority
- US
- United States
- Prior art keywords
- flotation
- per cent
- froth flotation
- pulp
- emulsifying
- 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
- 238000009291 froth flotation Methods 0.000 title description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 239000003995 emulsifying agent Substances 0.000 description 8
- 238000005188 flotation Methods 0.000 description 8
- 239000000126 substance Substances 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 239000004359 castor oil Substances 0.000 description 5
- 235000019438 castor oil Nutrition 0.000 description 5
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 4
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 4
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 4
- 239000005642 Oleic acid Substances 0.000 description 4
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 4
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- 239000010802 sludge Substances 0.000 description 4
- 230000001804 emulsifying effect Effects 0.000 description 3
- 239000010436 fluorite Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 235000004443 Ricinus communis Nutrition 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- WGPCGCOKHWGKJJ-UHFFFAOYSA-N sulfanylidenezinc Chemical compound [Zn]=S WGPCGCOKHWGKJJ-UHFFFAOYSA-N 0.000 description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910052586 apatite Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000881 depressing effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- -1 hydroxyl- Chemical group 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- JQJCSZOEVBFDKO-UHFFFAOYSA-N lead zinc Chemical compound [Zn].[Pb] JQJCSZOEVBFDKO-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 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 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000002367 phosphate rock Substances 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910052950 sphalerite Inorganic materials 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- B03D1/001—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
- 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
- B03D2201/002—Coagulants and Flocculants
-
- 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
- B03D2201/007—Modifying reagents for adjusting pH or conductivity
-
- 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
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/04—Frothers
Definitions
- oil-solubl emulsifying agents of the kind of the reaction products of alkylene oxides on aliphatic or aromatic compounds containing hydroxyl-, carboxylor aminogroups do not disturb the flotation and maintain their emulsifying action even if the usual reagents at best sparingly soluble in water and admixed.
- the said emulsifying agents are characterized by the eneral formula wherein R stands for a member of the group consisting of alkyl, aryl, aralkyl and hydroaromatic groups, X stands for a member of the group consisting of NH, O and COO, n is a whole number greater than 1 and m is a whole number, i. e., they contain a number of alkylene oxide groups in an ether-like chain.
- R stands for a member of the group consisting of alkyl, aryl, aralkyl and hydroaromatic groups
- X stands for a member of the group consisting of NH, O and COO
- n is a whole number greater than 1
- m is a whole number, i. e., they contain a number of alkylene oxide groups in an ether-like chain.
- the emulsifying agents named are readily soluble in water and as the flotation substance is added to th sludge in
- the floating agents according to the invention may be used for all non-metallic minerals, particularly the so-called oxidic and sulphidic ores, for instance phosphorite, apatite, fluorite, tungstite, scheelite, chromite, native tin, calcite, heavy spar, as well as the oxides, carbonates, sulfides or the like of the heavy metals, and others.
- oxidic and sulphidic ores for instance phosphorite, apatite, fluorite, tungstite, scheelite, chromite, native tin, calcite, heavy spar, as well as the oxides, carbonates, sulfides or the like of the heavy metals, and others.
- Fluorspar (fluorite) from the mountains Hartz (Germanv) containing 82.8 per cent. of CaFz, 11.8 per cent. of SiO: and 3.5 per cent. of Fe2O3+A12O3 and comminuted to a granular size of 61.8 per cent. smaller than 0.06 millimeter is worked up (a) with 450 grams per ton of oleic acid containing 5 per cent of higher hydroxyethylated castor oil (with 40 hydroxy-ethyl groups), (b) only with 450 grams per ton of oleic acid as a collector.
- frothing agent 30 parts by weight of a usual frothing substance, for instance pine oil or terpene alcohol.
- castor oil hydroxy-ethylated with 40 mol of ethylene oxide there may be used lower hydroxy-alkylated products for the purposes in question, for instance the reaction products with only 20 or mol of ethylene oxide.
- emulsifying agents there are furthermore suitable higher hydroxy-ethylated sperm oil alcohols, hydroxy-ethylated oleylamlne with 10 mol of ethylene oxide, higher hydroxy-ethylated alkylated phenols for instance with 20 to mol of ethylene oxide or the like.
- the addition of sulphonated castor oil in froth flotation is known, but this is not the object of the present invention.
Landscapes
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Description
Patented Nov. 17, 1942 FROTH FLOTATION August Moeller and Ernst Wagner, Frankfort-onthe-Main-Griesheim, Germany; vested in the Allen Property Custodian No Drawing. Application May 11, 1939, Serial No. 273,144. In Germany May 18, 1938 2 Claims. (Cl- 209-166) The present invention relates to froth flotation.
If sparingly soluble reagents are used in flotation processes they can rapidly and extensively be distributed in the pulp or sludge only with difliculty. It has hitherto been necessary to add said substances already in the mill and to put up with the difliculties connected therewith in the screening, such as a premature foaming or the like; the eflicacy of the substances however could not be entirely utilized thereby.
Attempts have, therefore, been made to emulsify the reagents (see W. Peterson, Metall und Erz," vol. 34, 1937, p ge 367). As the usual emulsifying agents, such as soaps and wetting agents, may have a disturbing action on the flotation process, by either decreasing the effect of the collector or by having a collecting action on the gangue (for instance in the case of sulphidic ores) and as furthermore a relatively large quantity of the emulsifying agent is required, which has a detrimental action upon the formation of froth and makes its application expensive, such a method of operatingv has not been found useful for industrial purposes.
Further attempts have been made to add the sparingly soluble or insoluble reagents in the form of alcoholic solutions to the sludge or to emulsify them by the treatment with ultra sound waves. As in the first named casea multipl quantity of alcohol calculated upon the quantity of the reagent has to be added, and as in the last named case a complicated apparatus showing the inferior effect has been necessary, both processes have likewise not been applied for industrial purposes.
Now we have found that oil-solubl emulsifying agents of the kind of the reaction products of alkylene oxides on aliphatic or aromatic compounds containing hydroxyl-, carboxylor aminogroups do not disturb the flotation and maintain their emulsifying action even if the usual reagents at best sparingly soluble in water and admixed.
with only a small quantity of these bodies are added to the sludge in the usual proportions. The said emulsifying agents are characterized by the eneral formula wherein R stands for a member of the group consisting of alkyl, aryl, aralkyl and hydroaromatic groups, X stands for a member of the group consisting of NH, O and COO, n is a whole number greater than 1 and m is a whole number, i. e., they contain a number of alkylene oxide groups in an ether-like chain. As the emulsifying agents named are readily soluble in water and as the flotation substance is added to th sludge in a proportion of 1:4000 to 1:40.000, 1. e., 100,000 to 1 million parts and more of water are used for 1 part of emulsifying substance, it is surprising that the emulsifying effect is maintained in spite Of the high dilution.
In view of these two facts it is possible to carry out the flotation in a simple manner by means of very sparingly soluble or insoluble reagents by mixing the reagent in question with the small quantity of emulsifying agent required (for instance 2 to 5 per cent) and adding the mixture to the pulp directly before it is or after it has been introduced into the flotation 'vessel. The insoluble reagent distributes at once just as a watersoluble substance and is completely effective. Owing to the improved distribution the sparingly soluble or insoluble reagents may rapidly and readily reach the places where they have to be effective. By the application of a reagent thus emulsified the flotation is simplified and acceler ated and owing to the better utilization a large quantity of reagents can be saved.
The floating agents according to the invention may be used for all non-metallic minerals, particularly the so-called oxidic and sulphidic ores, for instance phosphorite, apatite, fluorite, tungstite, scheelite, chromite, native tin, calcite, heavy spar, as well as the oxides, carbonates, sulfides or the like of the heavy metals, and others.
The following examples serve to illustrate the invention, but they are not intended to limit it thereto:
1. Fluorspar (fluorite) from the mountains Hartz (Germanv) containing 82.8 per cent. of CaFz, 11.8 per cent. of SiO: and 3.5 per cent. of Fe2O3+A12O3 and comminuted to a granular size of 61.8 per cent. smaller than 0.06 millimeter is worked up (a) with 450 grams per ton of oleic acid containing 5 per cent of higher hydroxyethylated castor oil (with 40 hydroxy-ethyl groups), (b) only with 450 grams per ton of oleic acid as a collector.
Proportion of the pulp: 1:5; reaction period: 5 minutes.
(b) Oleic acid without emulsifying agent Per cent Per cent Yield of Product by weight of CaF; Cal",
2. A lead-zinc ore originated from the mine Hiils" (Westphalia, Germany) containing about 7 per cent. of Pb and comminuted to a granular size of v71.9 per cent smaller than 0.076 millimeter is worked up (a) with 45 grams per ton of ethyldixanthogene containing per cent. of higher hydroxyethylated castor 011 (1)) only with 45 grams per ton of ethyldixanthogene as a collector. The reaction period amounts to 5 minutes in each case.
Addition of frothing agent: 30 parts by weight of a usual frothing substance, for instance pine oil or terpene alcohol.
For depressing the zinc blende (sphalerite) there are added:
Grams NaCN per t -200 ZnSOr per ton 200 Sodium carbonate per ton 500 G110 per ton 800 Proportion of the pulp: 1:3.5. Temperature of the pulp: 20 C. Flotation period: 15 minutes. After activation of the zinc blende it can be floated out with (a), but not with (b). As a standard of comparison does not exist, the zinc is not valued. As regards the lead the following figures are obtained:
Instead of the castor oil hydroxy-ethylated with 40 mol of ethylene oxide there may be used lower hydroxy-alkylated products for the purposes in question, for instance the reaction products with only 20 or mol of ethylene oxide. As emulsifying agents there are furthermore suitable higher hydroxy-ethylated sperm oil alcohols, hydroxy-ethylated oleylamlne with 10 mol of ethylene oxide, higher hydroxy-ethylated alkylated phenols for instance with 20 to mol of ethylene oxide or the like. The addition of sulphonated castor oil in froth flotation is known, but this is not the object of the present invention.
We claim:
1. In a method of froth flotation, the step of agitating and aerating a pulp of an ore in the presence of oleic acid and a higher hydroxyethylated castor oil obtained by the addition of 40 mols of ethylene oxide to one mol of castor 0 oil.
castor oil. I
AUGUST MOELIER. ERNST WAGNER.
CERTIFICATE OF CORRECTION. Patent- No. 2, 02, 58. Novem'ber 17, 191 2. AUGUST MOELLER, ET AL.
It is hereby certified that error appears 1n the printed specification ofthe'abo've numbered patent requiring correction as follows: Page 2 0nd column, line 26, claim 1; for the words- "an ore" read -'-a non-metallic ore--; line 56, claim 2, after f'oil. insert the-following claim sec- 5. In a method of froth flotation, the step of agitating and aerating a pulp of a non-metallic ore in the presence of oleic acid' and a higher hydroxiethylated castor oil obtained by the addition of from 20 to 1+0 mole of ethylene oxide to one mol of castor oil.
in the heading to the printed specification, line 8, for "2 Claims read "5 Claims--; and that the said Letters Patent should be read with this correction therein that the same 'may conform to the record gf the case in the Patent Office.
Signed and sealed this 15th day of August, A. D. 19bit.
Leslie Frazer (Seal) Acting Commissioner of Patents.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2302338X | 1938-05-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2302338A true US2302338A (en) | 1942-11-17 |
Family
ID=7994197
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US273144A Expired - Lifetime US2302338A (en) | 1938-05-18 | 1939-05-11 | Froth flotation |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2302338A (en) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3122500A (en) * | 1962-01-24 | 1964-02-25 | Magnet Cove Barium Corp | Flotation of barite |
| US3640382A (en) * | 1970-02-04 | 1972-02-08 | Basic Inc | Flotation concentration of magnesite with emulsified collector reagents |
| US3780860A (en) * | 1971-05-17 | 1973-12-25 | Stephan Chem Co | Flotation of copper sulfide ores |
| US3827557A (en) * | 1971-05-17 | 1974-08-06 | Stepan Chemical Co | Method of copper sulfide ore flotation |
| US3837489A (en) * | 1972-11-24 | 1974-09-24 | Nalco Chemical Co | Molybdenum disulfide flotation antifoam |
| US3865718A (en) * | 1972-12-07 | 1975-02-11 | Dow Chemical Co | Frothers for the flotation of sulfidic ores |
| US4034863A (en) * | 1975-12-22 | 1977-07-12 | American Cyanamid Company | Novel flotation agents for the beneficiation of phosphate ores |
| 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 |
| US4110207A (en) * | 1976-01-05 | 1978-08-29 | American Cyanamid Company | Process for flotation of non-sulfide ores |
| US4176058A (en) * | 1974-10-24 | 1979-11-27 | Grobler Jacobus J | Method means for de-silting water |
| FR2429043A1 (en) * | 1978-06-22 | 1980-01-18 | Outokumpu Oy | Selective foam flotation process for mineral ores - using polysaccharide, lignosulphonate, surfactant etc. as additives (SW 28.1.80) |
| US4191655A (en) * | 1977-07-07 | 1980-03-04 | Betz Laboratories, Inc. | Dewatering composition |
| US4211644A (en) * | 1976-11-26 | 1980-07-08 | Pennwalt Corporation | Froth flotation process and collector composition |
| US4291004A (en) * | 1979-09-28 | 1981-09-22 | Betz Laboratories, Inc. | Process for removing sulfur dioxide from flue gas |
| US4337149A (en) * | 1981-05-11 | 1982-06-29 | Sherex Chemical Company, Inc. | Promoters for use in the anionic circuit of froth flotation of mineral ores |
| US4430238A (en) | 1981-05-18 | 1984-02-07 | Berol Kemi Ab | Esterified dicarboxylic acid and its use |
| US4526696A (en) * | 1982-10-13 | 1985-07-02 | Societe Nationale Elf Aquitaine (Production) | Flotation of minerals |
| US4732666A (en) * | 1985-10-25 | 1988-03-22 | Sentrachem Limited | Froth flotation |
| US4789466A (en) * | 1985-05-11 | 1988-12-06 | Henkel Kommanditgesellschaft Auf Aktien | Method of separating non-sulfidic minerals by flotation |
| WO2018114741A1 (en) | 2016-12-23 | 2018-06-28 | Akzo Nobel Chemicals International B.V. | Process to treat phosphate ores |
-
1939
- 1939-05-11 US US273144A patent/US2302338A/en not_active Expired - Lifetime
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3122500A (en) * | 1962-01-24 | 1964-02-25 | Magnet Cove Barium Corp | Flotation of barite |
| US3640382A (en) * | 1970-02-04 | 1972-02-08 | Basic Inc | Flotation concentration of magnesite with emulsified collector reagents |
| US3780860A (en) * | 1971-05-17 | 1973-12-25 | Stephan Chem Co | Flotation of copper sulfide ores |
| US3827557A (en) * | 1971-05-17 | 1974-08-06 | Stepan Chemical Co | Method of copper sulfide ore flotation |
| US3837489A (en) * | 1972-11-24 | 1974-09-24 | Nalco Chemical Co | Molybdenum disulfide flotation antifoam |
| US3865718A (en) * | 1972-12-07 | 1975-02-11 | Dow Chemical Co | Frothers for the flotation of sulfidic ores |
| US4176058A (en) * | 1974-10-24 | 1979-11-27 | Grobler Jacobus J | Method means for de-silting water |
| 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 |
| US4034863A (en) * | 1975-12-22 | 1977-07-12 | American Cyanamid Company | Novel flotation agents for the beneficiation of phosphate ores |
| US4110207A (en) * | 1976-01-05 | 1978-08-29 | American Cyanamid Company | Process for flotation of non-sulfide ores |
| US4211644A (en) * | 1976-11-26 | 1980-07-08 | Pennwalt Corporation | Froth flotation process and collector composition |
| US4191655A (en) * | 1977-07-07 | 1980-03-04 | Betz Laboratories, Inc. | Dewatering composition |
| FR2429043A1 (en) * | 1978-06-22 | 1980-01-18 | Outokumpu Oy | Selective foam flotation process for mineral ores - using polysaccharide, lignosulphonate, surfactant etc. as additives (SW 28.1.80) |
| US4291004A (en) * | 1979-09-28 | 1981-09-22 | Betz Laboratories, Inc. | Process for removing sulfur dioxide from flue gas |
| US4337149A (en) * | 1981-05-11 | 1982-06-29 | Sherex Chemical Company, Inc. | Promoters for use in the anionic circuit of froth flotation of mineral ores |
| US4430238A (en) | 1981-05-18 | 1984-02-07 | Berol Kemi Ab | Esterified dicarboxylic acid and its use |
| US4526696A (en) * | 1982-10-13 | 1985-07-02 | Societe Nationale Elf Aquitaine (Production) | Flotation of minerals |
| US4789466A (en) * | 1985-05-11 | 1988-12-06 | Henkel Kommanditgesellschaft Auf Aktien | Method of separating non-sulfidic minerals by flotation |
| US4732666A (en) * | 1985-10-25 | 1988-03-22 | Sentrachem Limited | Froth flotation |
| WO2018114741A1 (en) | 2016-12-23 | 2018-06-28 | Akzo Nobel Chemicals International B.V. | Process to treat phosphate ores |
| US20200222914A1 (en) * | 2016-12-23 | 2020-07-16 | Akzo Nobel Chemicals International B.V. | Process to treat phosphate ores |
| US11607696B2 (en) * | 2016-12-23 | 2023-03-21 | Nouryon Chemicals International B.V. | Process to treat phosphate ores |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2302338A (en) | Froth flotation | |
| US2950818A (en) | Flotation process | |
| US2373305A (en) | Tungsten ore flotation | |
| US3570772A (en) | Di(4-5 carbon branched primary alkyl) dithiophosphate promoters for the flotation of copper middlings | |
| CA1273024A (en) | Process and compound for the froth flotation beneficiation of iron minerals from iron ores | |
| US3590999A (en) | Flotation of sulfide ores | |
| US2811255A (en) | Process for recovery of molybdenite from copper sulfide-molybdenite flotation concentrates | |
| US2492936A (en) | Differential froth flotation of sulfide ores | |
| US4587013A (en) | Monothiophosphinates as acid, neutral, or mildly alkaline circuit sulfide collectors and process for using same | |
| US7011216B2 (en) | Process for the beneficiation of sulfide minerals | |
| US2310240A (en) | Flotation of ores | |
| US5261539A (en) | Flotation process for purifying calcite | |
| US3355017A (en) | Method for effecting ore flotation | |
| US6988623B2 (en) | Beneficiation of sulfide minerals | |
| US4220525A (en) | Beneficiation of metallic ores by froth flotation using polyhydroxy amine depressants | |
| US3037627A (en) | Method of beneficiating sulfide and oxide ores of copper, manganese, lead and zinc | |
| US3788467A (en) | Flotation process for recovering molybdenum | |
| US3623605A (en) | Process for the flotation of fluorite | |
| US4159943A (en) | Froth flotation of ores using hydrocarbyl bicarbonates | |
| MXPA05003708A (en) | Process for the beneficiation of sulfide minerals. | |
| US4530758A (en) | Ore flotation method | |
| US2238439A (en) | Froth flotation process | |
| US3182798A (en) | Process of recovering cassiterite from ores | |
| US2450720A (en) | Froth flotation of silicious gangue from an alkaline magnetic iron ore pulp with an amine | |
| US2628717A (en) | Flotation of ores |