[go: up one dir, main page]

US2724500A - Process for concentration of nonsulfide metallic minerals by froth flotation - Google Patents

Process for concentration of nonsulfide metallic minerals by froth flotation Download PDF

Info

Publication number
US2724500A
US2724500A US418778A US41877854A US2724500A US 2724500 A US2724500 A US 2724500A US 418778 A US418778 A US 418778A US 41877854 A US41877854 A US 41877854A US 2724500 A US2724500 A US 2724500A
Authority
US
United States
Prior art keywords
pulp
ore
flotation
sulfide
mineral
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
Application number
US418778A
Inventor
Stuart R Zimmerley
Martin W Wilson
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kennecott Corp
Original Assignee
Kennecott Copper Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kennecott Copper Corp filed Critical Kennecott Copper Corp
Priority to US418778A priority Critical patent/US2724500A/en
Application granted granted Critical
Publication of US2724500A publication Critical patent/US2724500A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/02Froth-flotation processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/012Organic compounds containing sulfur
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/02Collectors
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2201/00Specified effects produced by the flotation agents
    • B03D2201/04Frothers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B03SEPARATION 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
    • B03DFLOTATION; DIFFERENTIAL SEDIMENTATION
    • B03D2203/00Specified materials treated by the flotation agents; Specified applications
    • B03D2203/02Ores
    • B03D2203/04Non-sulfide ores
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S209/00Classifying, separating, and assorting solids
    • Y10S209/901Froth flotation; copper

Definitions

  • This invention relates to the recovery of various metallic minerals of non-sulfide character from their ores by froth flotation, and is concerned especially with the application of particular reagents to the ore during the processing thereof for the purpose of modifying or activating the valued mineral particles, to render them amenable (or more amenable than they would otherwise be) to the action of collector reagents.
  • Modification or activation is a Well-known phenomenon in the art of froth flotation, and usually involves surface alteration of the valued mineral particles to be recovered, as, for example, in the sulfidization of nonsulfide metallic mineral particles so that the common sulfide collectors will act to selectively float such particles relative to gangue constituents of the ore pulp.
  • the activation may be due in whole or part to other factors which are too complex to be readily ascertained, but which are adequately evidenced by results obtained in practice.
  • one of a group of organic compounds heretofore proposed as a collector reagent in flotation practice applying to sulfide minerals is utilized as a modifier or activator in connection with various non-sulfide metallic minerals, usually by means of a conditioning stage carried out immediately in advance of aeration of the pulp.
  • the group of organic compounds concerned is the thioamides, represented by the formula R.CS.NH2. While, from numerous tests made, it is reasonable to suppose that all members of this group are useful to a greater or lesser extent, considering the particular ore to which applied, including those instances where R is either aliphatic or aromatic, we have obtained especially worthwhile results from that portion of the group where R is CnH2n+l, n being any whole integer from to 4, and from mixtures of members of such group. Of this more lim ited group of compounds, thioacetamide has proven of greatest all around usefulness.
  • the process of the invention has been applied with particular success to many ores containing non-sulfide minerals of heavy metals, which minerals have hereto fore been diflicult or even impossible to float by the use of known processes.
  • the mineral anglesite (a lead sulphate) has not heretofore been successfully floated by any known process, from ores or artificial mixtures containing same, yet excellent recoveries have been consistently made in tests applying the process of this invention.
  • the mineral cerussite (a lead carbonate) and the minerals malachite and azurite (both copper carbonates) have been floated heretofore only with difficulty, yet very satisfactory recoveries have been easily made utilizing the present process.
  • One of the outstanding advantages of the invention is the fact that not only can better recoveries be made than heretofore in instances of these and other non-sulfide metallic ores, such as oxidized copper ores, but considerable savings can be eflected in the consumption of collector and frother reagents as compared with pulps not so treated and with conventionally sulfidized pulps.
  • a characteristic of the process is the persistence of the activation. Once applied, no stage additions of the reagent are required during the course of the flotation procedure.
  • Standard pH control techniques are substantially unafiected by the present process, and should be applied where indicated by the character of the particular ore being treated and of the particular reagents utilized.
  • the reagent of the invention may be applied to the ore in various conventional ways, for example, in the grinding circuit, in an advance conditioning stage, or during the flotation stage immediately prior to the application of the collector and frother reagents. Generally, however, it has been found most desirable to apply the reagent to the ore pulp, and to condition the mixture by agitation for a few minutes prior to the addition of the collector and frothing agents and prior to the commencement of aeration.
  • collectors and frothers are ordinarily employed, as indicated by the particular ore being treated.
  • oxidized copper ore from the Bingham Canyon properties of Utah Copper Division, Kennecott Copper Corporation
  • butyl xanthate has proven very satisfactory as the collector and pine oil as the frother.
  • benzothiazole has operated successfully as the collector reagent in the recovery of the lead mineral from an artificial mixture of cerussite (lead carbonate), siderite, oxidized copper ore, and calcite,'pine oil being employed as the frother.
  • cerussite lead carbonate
  • siderite siderite
  • oxidized copper ore and calcite,'pine oil
  • thioacetamide was the activator reagent in accordance with the invention.
  • the ore utilized for this example was that mentioned above as being a naturally occurring oxidized copper obtained from the properties of Utah Copper Division, Kennecott Copper Corporation in Bingham Canyon, Utah.
  • tests of this example were made on respective 500 gram quantities of the ore, and were identical except that the ore was not activated in test No. 2.
  • Butyl xanthate was used as the collector, on a quantitative basis of 0.9 lb. per ton of the ore, and both pine oil and Dow' froth were used as frothing agents, on the basis of 0.1 lb. per ton, respectively.
  • the thioacetamide was added to the prepared-ore pulp, in test No. 1, on the basis of 0.5 lb. per ton, prior to the addition of the collector and frother reagents, and the pulp was agitated for 5 minutes without aeration.- The other reagents were added in stages during the course of aeration of the so-conditioned pulp.
  • the above-mentioned artificial mix ture of cerussite (lead carbonate), siderite, oxidized copper, and calcite was utilized, there being 60 gms., 5 gms., 430 gms., and 5 gms., respectively, of the component materials, making an over-all quantity of 500 gms., as in Example No. l.
  • Example No. l benzothiazole being employed as the collector reagent in both tests on a quantitative basis of 1.2 lbs. per ton.
  • the frother reagent was pine oil, added to the pulp on the basis of 0.15 lb. per ton.
  • R represents CnHzn-z-i and n is any whole integer from 0 to 4.
  • a process of concentrating non-sulfide minerals of heavy metals from ores containing same comprising forming a flotation pulp of said ore; conditioning said pulp with a thioarnide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
  • a process of concentrating non-sulfide minerals of heavy metals from ores containing same comprising forming a flotation pulp of said ore; conditioning said pulp with a substance conforming to the following general formula:
  • R represents CnHZn-H.
  • n is any whole integer from 0 to 4; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
  • a process of concentrating non-sulfide minerals of heavy metals from ores containing same comprising forming a flotation pulp of said ore; conditioning said pulp with a thio alkyl amide, the alkyl radical having not more than four carbon atoms; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
  • a process of concentrating non-sulfide minerals of heavy metals from ores containing same comprising forming a flotation pulp of said ore; conditioning said pulp with a thioformamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
  • a process of concentrating non-sulfide minerals of heavy metals from ores containing same comprising forming a flotation pulp of said ore; conditioning said pulp with a thioacetamide; and subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered.
  • a process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting ofnonsulfide minerals of copper and lead comprising forming a flotation pulp of said ore; conditioning said pulp with a thioamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said. mineral to be recovered.
  • a process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting of nonsulfide minerals of copper and lead, comprising forming a flotation pulp of said ore; conditioning said pulp with a substance conforming to the following general formula:
  • R represents cnH2n+l a thio alkyl amide, the alkyl radical having not more than four carbon atoms; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
  • a process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting of nonsulfide minerals of copper and lead comprising forming a flotation pulp of said ore; conditioning said pulp with a thioformamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
  • a process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting of nonsulfide minerals of copper and lead comprising forming a flotation pulp of said ore; conditioning said pulp with a thioacetamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.

Landscapes

  • Manufacture And Refinement Of Metals (AREA)

Description

an... a...-
United States Patent Ofice 2,7245% Patented Nov. 22, 1955 PROCFAQS FOR CONCENTRATION OF NON- SULFIDE METALLIC MINERALS BY FROTH FLOTATION Stuart R. Zimmcrley and Martin W. Wilson, Salt Lake City, Utah, assignors to Kennecott Copper Corporation, a corporation of New York No Drawing. Application March 25, 1954, Serial No. 418,778
15 Claims. (Cl. 209166) This invention relates to the recovery of various metallic minerals of non-sulfide character from their ores by froth flotation, and is concerned especially with the application of particular reagents to the ore during the processing thereof for the purpose of modifying or activating the valued mineral particles, to render them amenable (or more amenable than they would otherwise be) to the action of collector reagents. v
Modification or activation is a Well-known phenomenon in the art of froth flotation, and usually involves surface alteration of the valued mineral particles to be recovered, as, for example, in the sulfidization of nonsulfide metallic mineral particles so that the common sulfide collectors will act to selectively float such particles relative to gangue constituents of the ore pulp. However, the activation may be due in whole or part to other factors which are too complex to be readily ascertained, but which are adequately evidenced by results obtained in practice.
In accordance with the present invention, one of a group of organic compounds heretofore proposed as a collector reagent in flotation practice applying to sulfide minerals is utilized as a modifier or activator in connection with various non-sulfide metallic minerals, usually by means of a conditioning stage carried out immediately in advance of aeration of the pulp.
The group of organic compounds concerned is the thioamides, represented by the formula R.CS.NH2. While, from numerous tests made, it is reasonable to suppose that all members of this group are useful to a greater or lesser extent, considering the particular ore to which applied, including those instances where R is either aliphatic or aromatic, we have obtained especially worthwhile results from that portion of the group where R is CnH2n+l, n being any whole integer from to 4, and from mixtures of members of such group. Of this more lim ited group of compounds, thioacetamide has proven of greatest all around usefulness.
The process of the invention has been applied with particular success to many ores containing non-sulfide minerals of heavy metals, which minerals have hereto fore been diflicult or even impossible to float by the use of known processes. For example, the mineral anglesite (a lead sulphate) has not heretofore been successfully floated by any known process, from ores or artificial mixtures containing same, yet excellent recoveries have been consistently made in tests applying the process of this invention. Likewise the mineral cerussite (a lead carbonate) and the minerals malachite and azurite (both copper carbonates) have been floated heretofore only with difficulty, yet very satisfactory recoveries have been easily made utilizing the present process.
One of the outstanding advantages of the invention is the fact that not only can better recoveries be made than heretofore in instances of these and other non-sulfide metallic ores, such as oxidized copper ores, but considerable savings can be eflected in the consumption of collector and frother reagents as compared with pulps not so treated and with conventionally sulfidized pulps.
A characteristic of the process is the persistence of the activation. Once applied, no stage additions of the reagent are required during the course of the flotation procedure.
Standard pH control techniques are substantially unafiected by the present process, and should be applied where indicated by the character of the particular ore being treated and of the particular reagents utilized.
The reagent of the invention may be applied to the ore in various conventional ways, for example, in the grinding circuit, in an advance conditioning stage, or during the flotation stage immediately prior to the application of the collector and frother reagents. Generally, however, it has been found most desirable to apply the reagent to the ore pulp, and to condition the mixture by agitation for a few minutes prior to the addition of the collector and frothing agents and prior to the commencement of aeration.
Conventional collectors and frothers are ordinarily employed, as indicated by the particular ore being treated. Thus, where treating oxidized copper ore from the Bingham Canyon properties of Utah Copper Division, Kennecott Copper Corporation, butyl xanthate has proven very satisfactory as the collector and pine oil as the frother. Again benzothiazole has operated successfully as the collector reagent in the recovery of the lead mineral from an artificial mixture of cerussite (lead carbonate), siderite, oxidized copper ore, and calcite,'pine oil being employed as the frother. In both of these instances thioacetamide was the activator reagent in accordance with the invention.
The beneficial and advantageous results obtainable by use of the new process in connection with normally diflicult or impossible to float, non-sulfide metallic ores, are indicated by the several typical examples set forth herebelow. Each example includes a set of comparative tests made, respectively, with and without activation in accordance with the invention.
Example No. 1
The ore utilized for this example was that mentioned above as being a naturally occurring oxidized copper obtained from the properties of Utah Copper Division, Kennecott Copper Corporation in Bingham Canyon, Utah.
The flotation procedure followed was normal in all respects, except for an initial conditioning of the pulp with thioacetamide, in test No. 1.
The tests of this example were made on respective 500 gram quantities of the ore, and were identical except that the ore was not activated in test No. 2. Butyl xanthate was used as the collector, on a quantitative basis of 0.9 lb. per ton of the ore, and both pine oil and Dow' froth were used as frothing agents, on the basis of 0.1 lb. per ton, respectively.
The thioacetamide was added to the prepared-ore pulp, in test No. 1, on the basis of 0.5 lb. per ton, prior to the addition of the collector and frother reagents, and the pulp was agitated for 5 minutes without aeration.- The other reagents were added in stages during the course of aeration of the so-conditioned pulp.
The following results were obtained:
Example N0. 2
For this example, the above-mentioned artificial mix ture of cerussite (lead carbonate), siderite, oxidized copper, and calcite was utilized, there being 60 gms., 5 gms., 430 gms., and 5 gms., respectively, of the component materials, making an over-all quantity of 500 gms., as in Example No. l.
The procedure corresponded to that followed in Example No. l, benzothiazole being employed as the collector reagent in both tests on a quantitative basis of 1.2 lbs. per ton. The frother reagent was pine oil, added to the pulp on the basis of 0.15 lb. per ton.
In test No. l, the pulp was agitated in the presence of thioacetamide, as an activator, the quantity utilized in this instance being on the basis of 1.2 lbs. per ton.
The following results were obtained:
Test N0. 1 Test No. 2 (Activated) (Not Activated) Cone. (grams) 74 16 Percent Oonc 14. 6 3. 2 Percent Pb 37. 5 19. 86 Percent Pb recover 73.2 10.8
Cone. (grams) 33 27 Percent Gone. 6. 5 5. 4 Percent Pb 22. 68 28. 61 Percent Pb recovery 19.7 26. 2
Cone. (grams) 12 16 Percent Gone. 2. 4 3. 2 Percent Pb 6. 2 23. 96 Percent Pb recovery. 2. 4 l3.
railings (grams) 387 438 Percent tailings. 76. 5 88. 2 Percent Pb 50 3.36 Percent Pb recovery 4. 7 50. 00
Total percent Pb recovery in concentrates".-. 95. 3 50. 00
The results obtained in the above examples of practical applications of our process are typical of what may be expected in the various procedures comprehended by the claims which here follow.
We claim:
1. In the process of concentrating non-sulfide minerals of heavy metals from ores containing same, the step of subjecting the ore in the form of a pulp to a flotation operation in the presence of an activating agent having the following general formula:
where R represents CnHzn-z-i and n is any whole integer from 0 to 4.
2. In the process of concentrating non-sulfide minerals of heavy metals from ores containing same, the step of subjecting the ore in the form of a pulp to a flotation operation in the presence of a thio alkyl amide as an activating agent, the alkyl radical of said agent having not more than four carbon atoms.
3. In the process of concentrating non-sulfide minerals from ores containing same, the step of subjecting the ore in the form of a pulp to a flotation operation in the presence of thioformamide as an activating agent.
4. In the process of concentrating non-sulfide minerals of heavy metals from ores containing same, the step of subjecting the ore in the form of a pulp to a flotation operation in the presence of thioacetamide as an activating agent.
5. In the process of concentrating non-sulfide minerals of heavy metals from ores containing same, the step of subjecting the ore in the form of a pulp to a flotation operation in the presence of a thioamide as an activating agent.
6. A process of concentrating non-sulfide minerals of heavy metals from ores containing same, comprising forming a flotation pulp of said ore; conditioning said pulp with a thioarnide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
7. A process of concentrating non-sulfide minerals of heavy metals from ores containing same, comprising forming a flotation pulp of said ore; conditioning said pulp with a substance conforming to the following general formula:
R--NH:
where R represents CnHZn-H.
and n is any whole integer from 0 to 4; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
8. A process of concentrating non-sulfide minerals of heavy metals from ores containing same, comprising forming a flotation pulp of said ore; conditioning said pulp with a thio alkyl amide, the alkyl radical having not more than four carbon atoms; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
9. A process of concentrating non-sulfide minerals of heavy metals from ores containing same, comprising forming a flotation pulp of said ore; conditioning said pulp with a thioformamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
10. A process of concentrating non-sulfide minerals of heavy metals from ores containing same, comprising forming a flotation pulp of said ore; conditioning said pulp with a thioacetamide; and subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered.
11. A process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting ofnonsulfide minerals of copper and lead, comprising forming a flotation pulp of said ore; conditioning said pulp with a thioamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said. mineral to be recovered.
12. A process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting of nonsulfide minerals of copper and lead, comprising forming a flotation pulp of said ore; conditioning said pulp with a substance conforming to the following general formula:
i R-iJ-NH; where R represents cnH2n+l a thio alkyl amide, the alkyl radical having not more than four carbon atoms; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
14. A process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting of nonsulfide minerals of copper and lead, comprising forming a flotation pulp of said ore; conditioning said pulp with a thioformamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
15. A process of concentrating a non-sulfide mineral of a heavy metal selected from the group consisting of nonsulfide minerals of copper and lead, comprising forming a flotation pulp of said ore; conditioning said pulp with a thioacetamide; subjecting the so conditioned pulp to froth flotation in the presence of collector and frother reagents specific to the non-sulfide metallic mineral to be recovered; and recovering a froth concentrate of the said mineral to be recovered.
OTHER REFERENCES Taggart: Handbook of Mineral Dressing, 1945, section 12, pages 120 and 121. (Copy in Scientific Library.)

Claims (1)

1. IN THE PROCESS OF CONCENTRATING NON-SULFIDE MINERALS OF HEAVY METALS FROM ORES CONTAINING SAME, THE STEP OF SUBJECTING THE ORE IN THE FORM OF A PULP TO A FLOTATION OPERATION IN THE PRESENCE OF AN ACTIVATING AGENT HAVING THE FOLLOWING GENERAL FORMULA:
US418778A 1954-03-25 1954-03-25 Process for concentration of nonsulfide metallic minerals by froth flotation Expired - Lifetime US2724500A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US418778A US2724500A (en) 1954-03-25 1954-03-25 Process for concentration of nonsulfide metallic minerals by froth flotation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US418778A US2724500A (en) 1954-03-25 1954-03-25 Process for concentration of nonsulfide metallic minerals by froth flotation

Publications (1)

Publication Number Publication Date
US2724500A true US2724500A (en) 1955-11-22

Family

ID=23659531

Family Applications (1)

Application Number Title Priority Date Filing Date
US418778A Expired - Lifetime US2724500A (en) 1954-03-25 1954-03-25 Process for concentration of nonsulfide metallic minerals by froth flotation

Country Status (1)

Country Link
US (1) US2724500A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4022686A (en) * 1975-03-13 1977-05-10 Sumitomo Metal Mining Co., Limited Flotation process for copper ores and copper smelter slags

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1863760A (en) * 1927-05-20 1932-06-21 Barrett Co Separation of minerals by flotation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1863760A (en) * 1927-05-20 1932-06-21 Barrett Co Separation of minerals by flotation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4022686A (en) * 1975-03-13 1977-05-10 Sumitomo Metal Mining Co., Limited Flotation process for copper ores and copper smelter slags

Similar Documents

Publication Publication Date Title
US5411148A (en) Selective flotation process for separation of sulphide minerals
CA1270076A (en) Collectors for the selective froth flotation of mineral sulfides
US4710361A (en) Gold recovery by sulhydric-fatty acid flotation as applied to gold ores/cyanidation tailings
US3138550A (en) Froth flotation process employing polymeric flocculants
US4256227A (en) Froth flotation method for recovering metal values from their ores by thiourea or substituted thiourea
US4387034A (en) Mixed alkylthionocarbamates flotation collectors and ore dressing methods in which the collectors are employed
US2310240A (en) Flotation of ores
US3059774A (en) Method and means for beneficiating ores
US2278060A (en) Mineral concentration
CA1267979A (en) Collector composition for froth flotation
US4054442A (en) Method for recovering scheelite from tungsten ores by flotation
CA2075155C (en) Process for improved precious metals recovery from ores with the use of alkylhydroxamate collectors
US3827557A (en) Method of copper sulfide ore flotation
US3469692A (en) Use of organic dithiols as flotation reagents
US2724500A (en) Process for concentration of nonsulfide metallic minerals by froth flotation
US2312387A (en) Froth flotation of acidic minerals
US4159943A (en) Froth flotation of ores using hydrocarbyl bicarbonates
US2467369A (en) Froth flotation of ores with aromatic alcohol
US4515688A (en) Process for the selective separation of base metal sulfides and oxides contained in an ore
US1952907A (en) Method of flotation of oxidized ores
US3822014A (en) Process of flotation of minterals and ores
US2130574A (en) Flotation of carbonaceous ores
US2446207A (en) Froth flotation of ores employing a water-soluble salt of a cymene sulfonic acid
RU2068739C1 (en) Method of extracting bismuth minerals from non-magnetic fraction produced when finishing rough tungsten concentrates
US2403640A (en) Separation of cobaltite