US2373305A - Tungsten ore flotation - Google Patents
Tungsten ore flotation Download PDFInfo
- Publication number
- US2373305A US2373305A US461199A US46119942A US2373305A US 2373305 A US2373305 A US 2373305A US 461199 A US461199 A US 461199A US 46119942 A US46119942 A US 46119942A US 2373305 A US2373305 A US 2373305A
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- United States
- Prior art keywords
- tungsten
- flotation
- ore
- concentrate
- promoter
- Prior art date
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Classifications
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- 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
- 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
- B03D1/016—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
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/04—Frothers
-
- 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
- B03D2201/06—Depressants
-
- 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
Definitions
- mon tungsten-bearing minerals such as scheelite usually occur with a mixed gangue including sulflde minerals such as pyrites, carbonates such as calcite and the like and silicon-containing minerals such as quartz and garnet.
- the domestic ores'could not be eflectively I
- the objects of the present invention are accomplished by subjecting the ore to a preliminary froth flotation to remove the sulfide minerals and then collecting the tungsten concentrate by the aid of an anionic-type promoter, assisted by a suitable wetting agent.
- a suitable depressant for the carbonates and silicon-bearing constituents is made. In this manner a ratio of concentration of I the tungsten mineral as high as to :1 may be easily made while still maintaining a good recovery.
- Soheelite for example, as a typical tungstate'ore, may be concentrated from a pure mineral pulp with a good anionic reagent of the fatty acid type such as oleic acid, talloel, their sodium, po-
- anionic-type-reagent alone is notsuffloient to produce the necessary concentration.
- a reagent capable of increasing the selectivity Y of the promoter is not only desirable but necessary.
- most of the commonly used carbonate and silica depressants also tend to depress the flotation of scheelite-and the like.
- the nature of the promoter must be considered since it is well known that many depressants used in froth flotation operations in addition to-their sheet on the mineral, may also either by their inherent nature or because'of the quantity required, directly affectthe I collecting power of the frother and promoter.
- the concentrating power or the anionic reagent used as a promoter for the tungsten mineral may be enhanced by 1 the addition of suitable quantities of an effective anionic-typewetting agent.
- wetting agents suitable for use excellent results may be obtained using substances such as KemenoLa commercial alkyl aryl sulionate, marketed by the Braun-Knecht-Heimann Company, and Aerosol its nature or the quantity required produce an adverse effect on the quality and collecting power of the froth.
- any desirable irother may be used in the present reagent combination. Excellent results were obtained, for example, using a higher aliphatic alcohol frother with an average carbon content of C1 and C8.
- the invention is not intended to be limited to the use of any particular frother. Other frothers may be used if and when it is desirable to do so.
- Tungsten itself, can be refined from these low grade materials by chemical processes.
- the tungsten content is so low, tremendous capacity is required for even a very low pro- I duction of final product.
- the necessity for maintaining this excessive capacity and the use of exwhich must be treated can be cut down to a point at which the chemical refining process of the tailing piles becomes economically practical.
- EXAMPLE 1 A number of samples of a tungsten ore table tailings from a Nevada ore containing scheelite,
- EXAMPLE 2 A sample treated as outlined above was further conditioned for 2 minutes after which, 0.03 #/ton of the same frother and 0.42 #/ton of oleic acid were added and a tungsten rougher flotation carried out for 6 minutes. The sulfide concentrate amounted to 4.34% of the total feed and the tungsten concentrate amounted to 23.54% of the weight of the feed assaying 0.88% W0: and 17.97% carbonate were obtained.
- Example 3 was repeated substituting an equal weight of Aerosol 0'1 for the Kemenol. concentrate of 4.93% and a tungsten concentrate of 31.4% of the weight of the feed assaying 0.85% W0: and 20.24% carbonate were obtained. It will be noted that whereas the substitution of Aerosol OT for the Kemenol reduced the grade from 0.94% to 0.85%, the recovery was raised from 23.19% to 31.14% of the ore by weight. The net tungsten recovery in the concentrate was increased by about 20% so as to produce a recovery of approximately 78% of the total W03 content of the flotation feed.
- the tungsten concentrate also contained a high percentage of the carbonate and insoluble content of the flotation feed so that the grade, while improved in the ratio 01 about 2 to 32:1, is still too low for practical purposes.
- Example 2 The procedure of Example 2 was repeated using 0.037 #/ton of frother, 0.42 #/ton of oleic acid and 0.20 #/ton of quebracho present duringthe conditioning period and the tungsten concentrate was floated for 2 minutes. The results are shown It will be noted that the use of quebracho has increased the grade from the 0.88% in Example 2 to 6.98%, a ratio of concentration of about 38::1. Quebracho is therefore effective in depressing the carbonate and insoluble gangue.-
- Example 5 The procedure of Example 5 was repeated with the addition, however, of 0.0! #/ton of Aerosol '1 to the reagents during the conditioning period. The results are shown in the following table:
- the use or the depressant together with an anionic promoter assisted by the wetting agent produces a ratio of concentration of about 25: :1 and enables recovery of about 01' the W0: content even of the extremely low grade material which comprised the discard from previous beneflciation processes.
- a method of concentrating tungstate minerals from ores containing carbonate and silicon-bearing g'angue by means of froth flotation comprising carrying out the flotation step in the presence of a reagent combination of an anionic promoter, selected from the group consisting of the higher aliphatic ,fatty acids, talloel, and the sodium, potassium and ammonium soaps thereof, an alkali salt of a dialkyl sulfosuccinate and a gangue defatty acids, talloel, and the sodium, potassium and ammonium soaps thereof, an alkali salt of a di-octyl sulfosuccinate and quebracho.
- an anionic promoter selected from the group consisting of the higher aliphatic ,fatty acids, talloel, and the sodium, potassium and ammonium soaps thereof, an alkali salt of a dialkyl sulfosuccinate and a gangue defatty acids, talloel, and the sodium, potassium
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- Manufacture And Refinement Of Metals (AREA)
Description
Patented Apr. 10,1945
-NlTED STATES PATENT "omen TUNGS'IEN'ORE M IATION Elmer William Giescke, one Greenwich, as-
signor to American 6 Company, New York, N.-Y., a corporation of Maine No Drawing. Application October 7, 1942', Serial No. 481,199 r 3 Claims, (@1- 209-166) mon tungsten-bearing minerals such as scheelite usually occur with a mixed gangueincluding sulflde minerals such as pyrites, carbonates such as calcite and the like and silicon-containing minerals such as quartz and garnet.
Past experience has shown that with the exception of a very few relatively high grade deconcentrated and refined on a commercially teasible basis by any hio'wn methods; Consequently the principal demand had to be supplied by refining imported ores of relatively higher e.
Thereexisted, therefore, a real need for a method suitable forthe concentration of the average low grade domestic ores.
It is, therefore, an object of the present invention to establish an improved froth flotation procedure adapted to concentrate low grade domestic ores. It is also an object of the present. invention to provide the froth flotation reagent combination suitable for carrying out such a procedure.
posits, the domestic ores'could not be eflectively I In general, the objects of the present invention are accomplished by subjecting the ore to a preliminary froth flotation to remove the sulfide minerals and then collecting the tungsten concentrate by the aid of an anionic-type promoter, assisted by a suitable wetting agent. At the same time use is made of a suitable depressant for the carbonates and silicon-bearing constituents. In this manner a ratio of concentration of I the tungsten mineral as high as to :1 may be easily made while still maintaining a good recovery.
I Since not all t n ores contain sulfide min- I 'erals as gangue, the initial flotation treatment to remove these materials is not always required. Therefore, the removal of sulfide gangue is not necessarily a part of the present invention. Where the sulfide materials must be removed a number of. commerciallyavailable sulfide promoters may be used. For example, anexcellent sulfide, conoentration may be made. by conditioning a pulp oi the ore with a suitable amount or sodium, potassium or ammonium dicresyl dithiophosphate and/or sodium secondary butyl xanthatc; adding a good nothing agent such as a higher aliphatic alcohol irother and then floatins out and collecting the sulfide concentrate.
' The tungsten concentration, with which the present invention is concerned, however, is fairly -critical both as to the combination of reagents 1 used and the manner in which they are added.
Soheelite, for example, as a typical tungstate'ore, may be concentrated from a pure mineral pulp with a good anionic reagent of the fatty acid type such as oleic acid, talloel, their sodium, po-
tassium or ammonium soaps and the like. However, these same anionic agents are also fairly good collectors for certain of the gangue constituents usually found after the removal of the sulfide minerals in atypical tungsten ore. 'Calcite, garnet and apatite are typical illustrations. Therefore, the use of the anionic-type-reagent alone is notsuffloient to produce the necessary concentration.
A reagent capable of increasing the selectivity Y of the promoter is not only desirable but necessary. Unfortunately, most of the commonly used carbonate and silica depressants also tend to depress the flotation of scheelite-and the like. Not only the nature of the depressant used but also the quantity required must be taken into consideration. Inaddition, the nature of the promoter must be considered since it is well known that many depressants used in froth flotation operations in addition to-their sheet on the mineral, may also either by their inherent nature or because'of the quantity required, directly affectthe I collecting power of the frother and promoter.
Although the reason for their action is not 4 fully understood, accordingto the present invention a few depressants have been found suitable tor use with the activated promoter of the present invention. Among the materials which may be used successfully for this purpose are citric acid, tannic acid, tetrasodium or potassium pyrophosphate and quebraoh'o. In the quantities required, the efiect on the ccplecting' power of the other reagents isnot too great. Quebracho is perhaps preferable since it is slightly more effective in depressing the gangue without producing an appreciably adverse effect on the other re-v agents.
As was mentioned above, the concentrating power or the anionic reagent used as a promoter for the tungsten mineral may be enhanced by 1 the addition of suitable quantities of an effective anionic-typewetting agent. Among the wetting agents suitable for use, excellent results may be obtained using substances such as KemenoLa commercial alkyl aryl sulionate, marketed by the Braun-Knecht-Heimann Company, and Aerosol its nature or the quantity required produce an adverse effect on the quality and collecting power of the froth.
Any desirable irother may be used in the present reagent combination. Excellent results were obtained, for example, using a higher aliphatic alcohol frother with an average carbon content of C1 and C8. The invention, however, is not intended to be limited to the use of any particular frother. Other frothers may be used if and when it is desirable to do so.
The particular quantities of promoter, depressant, activator and frother used will obviously vary with the exact materials being used. This istrue both with regard to the particular ore which is being treated and the particular reagents selected. The optimum proportions of each of the reagents used, however, can be readily determined in accordance with the particular combination being used and the characteristics of the ore to be treated.
In addition to the naturally occurring low grade tungsten ores there is also available considerable amountsoi discarded material from beneficiation processes which have been carried out on relatively high grade ores. These discards may take the form of tabletailings or tailings from previous flotation processes. While these discards are very low in tungsten content, usually assaying less than /2 of 1% W03 they may represent as high as from V to of the total tungsten content 01 the original ore. Since this discarded material represents a good proportion of the original content of tungsten in the ore it is desirable if possible to, recover at least a portion of it.
Tungsten, itself, can be refined from these low grade materials by chemical processes. However, because the tungsten content is so low, tremendous capacity is required for even a very low pro- I duction of final product. The necessity for maintaining this excessive capacity and the use of exwhich must be treated can be cut down to a point at which the chemical refining process of the tailing piles becomes economically practical.
The nature of the invention as well as the relative eifect of the different reagent components will be illustrated by the following examples showing the treatment of samples from low grade tailing piles such as those mentioned above. All parts are by weight unless otherwise noted.
EXAMPLE 1 A number of samples of a tungsten ore table tailings from a Nevada ore containing scheelite,
calcite, pyrite, quartz and garnet having an average assay of: 4
are given the following treatment. 600 parts of the feed was diluted to 22% solids with water and conditioned for 5% minutes without air in a Fagergren flotation machine using 0.074 #/ton of were then'given the treatments outlined in the following examples.
EXAMPLE 2 A sample treated as outlined above was further conditioned for 2 minutes after which, 0.03 #/ton of the same frother and 0.42 #/ton of oleic acid were added and a tungsten rougher flotation carried out for 6 minutes. The sulfide concentrate amounted to 4.34% of the total feed and the tungsten concentrate amounted to 23.54% of the weight of the feed assaying 0.88% W0: and 17.97% carbonate were obtained.
Exslurtn 3 "The procedure of Example 2 was repeated using 0.0? #/ton of Kemenol during the 2 minute conditiorung period in addition to the other reagents listed. A sulfide concentrate amounting to 5.34% of the feed and a tungsten concentrate of 23.19% of the weight of the feed assaying 0.94% W0: and 18.47% carbonate were obtained.
EXAMPLE 4 Example 3 was repeated substituting an equal weight of Aerosol 0'1 for the Kemenol. concentrate of 4.93% and a tungsten concentrate of 31.4% of the weight of the feed assaying 0.85% W0: and 20.24% carbonate were obtained. It will be noted that whereas the substitution of Aerosol OT for the Kemenol reduced the grade from 0.94% to 0.85%, the recovery was raised from 23.19% to 31.14% of the ore by weight. The net tungsten recovery in the concentrate was increased by about 20% so as to produce a recovery of approximately 78% of the total W03 content of the flotation feed.
In each of Examples 2-4- inclusive, however, the tungsten concentrate also contained a high percentage of the carbonate and insoluble content of the flotation feed so that the grade, while improved in the ratio 01 about 2 to 32:1, is still too low for practical purposes.
Exam 5 The procedure of Example 2 was repeated using 0.037 #/ton of frother, 0.42 #/ton of oleic acid and 0.20 #/ton of quebracho present duringthe conditioning period and the tungsten concentrate was floated for 2 minutes. The results are shown It will be noted that the use of quebracho has increased the grade from the 0.88% in Example 2 to 6.98%, a ratio of concentration of about 38::1. Quebracho is therefore effective in depressing the carbonate and insoluble gangue.-
However, the recovery is only about 55%.
' Exauru 6 The procedure of Example 5 was repeated with the addition, however, of 0.0! #/ton of Aerosol '1 to the reagents during the conditioning period. The results are shown in the following table:
Table III Percent Assays distribution Product Pomm Percent Carbonwo, ate
Sulfidcconcentratc 4.40 0.12 14.00 1.34 0.01 Tungsten concentrate...... .aes 0.04 35.2 04.34 8.96 'lailing 91.02 0.14 14.00 34.32 111.07 Feed 1. 100.00 0.373- 1503 100.00 100.00
It will be noted that the use or the depressant together with an anionic promoter assisted by the wetting agent produces a ratio of concentration of about 25: :1 and enables recovery of about 01' the W0: content even of the extremely low grade material which comprised the discard from previous beneflciation processes.
Iclaim:
1. In a method of concentrating tungstate minerals from ores containing carbonate and silicon-bearing g'angue by means of froth flotation, the improvement which comprises carrying out the flotation step in the presence of a reagent combination of an anionic promoter, selected from the group consisting of the higher aliphatic ,fatty acids, talloel, and the sodium, potassium and ammonium soaps thereof, an alkali salt of a dialkyl sulfosuccinate and a gangue defatty acids, talloel, and the sodium, potassium and ammonium soaps thereof, an alkali salt of a di-octyl sulfosuccinate and quebracho.
3'. In a method of concentrating scheeiite from ores containing carbonate and silicon-bearing gangue by means of froth flotation, the improvement which comprises carrying out the flotation step in the presence of an anionic promoter, selected from the group consisting of the higher aliphatic fatty acids, talloel, and the sodium,
potassium, and ammonium soaps thereof, an alkali salt of a di-alkyl sulfosuccinate and on bracho. I EIMER WILLIAM GIESEKE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US461199A US2373305A (en) | 1942-10-07 | 1942-10-07 | Tungsten ore flotation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US461199A US2373305A (en) | 1942-10-07 | 1942-10-07 | Tungsten ore flotation |
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| Publication Number | Publication Date |
|---|---|
| US2373305A true US2373305A (en) | 1945-04-10 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US461199A Expired - Lifetime US2373305A (en) | 1942-10-07 | 1942-10-07 | Tungsten ore flotation |
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| US (1) | US2373305A (en) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2607479A (en) * | 1948-02-04 | 1952-08-19 | California Research Corp | Agglomerate tabling of tungsten bearing ores |
| US2741364A (en) * | 1953-07-24 | 1956-04-10 | Molybdenum Corp | Preparatory treatment for froth flotation |
| US3078997A (en) * | 1961-02-24 | 1963-02-26 | Havens Richard | Flotation process for concentration of phenacite and bertrandite |
| US3447682A (en) * | 1967-07-03 | 1969-06-03 | Sylvania Electric Prod | Method for separating phosphors |
| US3779380A (en) * | 1971-10-12 | 1973-12-18 | Hercules Inc | Collector composition for ore flotation |
| US3915391A (en) * | 1972-07-17 | 1975-10-28 | Engelhard Min & Chem | Recovery of scheelite from ores by flotation |
| US4040519A (en) * | 1974-03-28 | 1977-08-09 | Nittetsu Mining Company, Ltd. | Froth flotation process for recovering sheelite |
| US4158623A (en) * | 1977-12-21 | 1979-06-19 | American Cyanamid Company | Process for froth flotation of phosphate ores |
| US4366050A (en) * | 1981-01-19 | 1982-12-28 | Amax Inc. | Scheelite flotation |
| US4488959A (en) * | 1981-09-21 | 1984-12-18 | Agar Gordon E | Scheelite flotation process |
| US4719009A (en) * | 1986-07-07 | 1988-01-12 | Cominco Ltd. | Silica depressant in froth flotation of sulfide ores |
| WO1992011091A1 (en) * | 1990-12-17 | 1992-07-09 | The Dow Chemical Company | Aryl monosulfonate collectors useful in the flotation of minerals |
| US5171427A (en) * | 1990-02-23 | 1992-12-15 | The Dow Chemical Company | Sulfonated and carboxylate collector compositions useful in the flotation of minerals |
| US20070012630A1 (en) * | 2004-12-23 | 2007-01-18 | Georgia-Pacific Resins, Inc. | Amine-aldehyde resins and uses thereof in separation processes |
| US20080017552A1 (en) * | 2004-12-23 | 2008-01-24 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US20080029460A1 (en) * | 2004-12-23 | 2008-02-07 | Georgia-Pacific Chemicals Llc. | Amine-aldehyde resins and uses thereof in separation processes |
| US7913852B2 (en) | 2004-12-23 | 2011-03-29 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US8092686B2 (en) | 2004-12-23 | 2012-01-10 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US8702993B2 (en) | 2004-12-23 | 2014-04-22 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
| CN105413855A (en) * | 2015-12-30 | 2016-03-23 | 中南大学 | Method for cleaning and purification of tungsten rough concentrate |
-
1942
- 1942-10-07 US US461199A patent/US2373305A/en not_active Expired - Lifetime
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2607479A (en) * | 1948-02-04 | 1952-08-19 | California Research Corp | Agglomerate tabling of tungsten bearing ores |
| US2741364A (en) * | 1953-07-24 | 1956-04-10 | Molybdenum Corp | Preparatory treatment for froth flotation |
| US3078997A (en) * | 1961-02-24 | 1963-02-26 | Havens Richard | Flotation process for concentration of phenacite and bertrandite |
| US3447682A (en) * | 1967-07-03 | 1969-06-03 | Sylvania Electric Prod | Method for separating phosphors |
| US3779380A (en) * | 1971-10-12 | 1973-12-18 | Hercules Inc | Collector composition for ore flotation |
| US3915391A (en) * | 1972-07-17 | 1975-10-28 | Engelhard Min & Chem | Recovery of scheelite from ores by flotation |
| US4040519A (en) * | 1974-03-28 | 1977-08-09 | Nittetsu Mining Company, Ltd. | Froth flotation process for recovering sheelite |
| US4158623A (en) * | 1977-12-21 | 1979-06-19 | American Cyanamid Company | Process for froth flotation of phosphate ores |
| US4366050A (en) * | 1981-01-19 | 1982-12-28 | Amax Inc. | Scheelite flotation |
| US4488959A (en) * | 1981-09-21 | 1984-12-18 | Agar Gordon E | Scheelite flotation process |
| US4719009A (en) * | 1986-07-07 | 1988-01-12 | Cominco Ltd. | Silica depressant in froth flotation of sulfide ores |
| US5171427A (en) * | 1990-02-23 | 1992-12-15 | The Dow Chemical Company | Sulfonated and carboxylate collector compositions useful in the flotation of minerals |
| WO1992011091A1 (en) * | 1990-12-17 | 1992-07-09 | The Dow Chemical Company | Aryl monosulfonate collectors useful in the flotation of minerals |
| US20070012630A1 (en) * | 2004-12-23 | 2007-01-18 | Georgia-Pacific Resins, Inc. | Amine-aldehyde resins and uses thereof in separation processes |
| US20080017552A1 (en) * | 2004-12-23 | 2008-01-24 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US20080029460A1 (en) * | 2004-12-23 | 2008-02-07 | Georgia-Pacific Chemicals Llc. | Amine-aldehyde resins and uses thereof in separation processes |
| US7913852B2 (en) | 2004-12-23 | 2011-03-29 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US8011514B2 (en) | 2004-12-23 | 2011-09-06 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US8092686B2 (en) | 2004-12-23 | 2012-01-10 | Georgia-Pacific Chemicals Llc | Modified amine-aldehyde resins and uses thereof in separation processes |
| US8127930B2 (en) | 2004-12-23 | 2012-03-06 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
| US8702993B2 (en) | 2004-12-23 | 2014-04-22 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
| US8757389B2 (en) | 2004-12-23 | 2014-06-24 | Georgia-Pacific Chemicals Llc | Amine-aldehyde resins and uses thereof in separation processes |
| US10150839B2 (en) | 2004-12-23 | 2018-12-11 | Ingevity South Carolina, Llc | Amine-aldehyde resins and uses thereof in separation processes |
| CN105413855A (en) * | 2015-12-30 | 2016-03-23 | 中南大学 | Method for cleaning and purification of tungsten rough concentrate |
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