US3844939A - Flotation separation of feldspar - Google Patents

Flotation separation of feldspar Download PDF

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US3844939A
US3844939A US00232280A US23228072A US3844939A US 3844939 A US3844939 A US 3844939A US 00232280 A US00232280 A US 00232280A US 23228072 A US23228072 A US 23228072A US 3844939 A US3844939 A US 3844939A
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flotation
feldspar
carbon atoms
sulfonate
froth
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A Katayanagi
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    • 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
    • B03D1/00Flotation
    • B03D1/001Flotation agents
    • B03D1/004Organic compounds
    • B03D1/01Organic compounds containing nitrogen
    • 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
    • B03D2203/00Specified materials treated by the flotation agents; specified applications
    • B03D2203/02Ores
    • B03D2203/04Non-sulfide ores

Definitions

  • the present invention relates to a process for the flotation of feldspars contained in feldspathic ores by ric acid for hydrofluoric acid as the activating agent and effecting the flotation using a combination of a higher aliphatic amine and a higher aliphatic or arousing a combination of a higher aliphatic amine salt and Y a higher aliphatic or aromatic sulfonate as the flotation reagents so that activation with hydrofluoric acid is unnecessary.
  • feldspars In conventional froth flotation, feldspars have been separated from the feldspathic ores in-which they occur generally by pulverizing an me into a proper particle range, classifying the particles according to size, subjecting them to an activation treatment with hydrofluoric acid, admixing them in water together with a collector (for example, an aliphatic amine) and a foaming agent (for example, pine oil), introducing air therein to cause bubbling, and recovering the feldspars in the froth or foam thus generated, leaving other constituents, such as quartz, as tailings.
  • a collector for example, an aliphatic amine
  • a foaming agent for example, pine oil
  • hydrofluoric acid is a highly poisonous reagent and, therefore, must be handled with the greatest possible care.
  • hydrofluoric acid has the disadvantage of attacking and dissolving the surface of the quartz with a reduction in the yield of the product. Complications are therefore presented in carrying out this process on a commercial scale.
  • an object of the present invention is to provide an improved process for the flotation, espe cially froth flotation, of feldspars from feldspathic ores.
  • Another object of the invention is to provide a process for the flotation of feldspar which does not require activation with hydrofluoric acid.
  • Still another object of the invention is to provide a novel flotation process for separating feldspars from feldspathic ores wherein a combination of a higher aliphatic amine salt and a higher aliphatic or aromatic sulfonate is used as the flotation reagent under an acidic condition provided by sulfuric acid.
  • the higher aliphatic amine salt used as one component of the flotation reagent in the present invention may be any higheraliphatic amine salt known to have utility as the so-called collector in conventional flotation processes.
  • These salts are cationic surfactants containing at least one amino group and having attached to the nitrogen atomsof one amino group thereof a long chain hydrocarbon group, saturated, unsaturated and mixtures thereof, containing at least about eight carbon atoms and preferably at least about l2 carbons.
  • the maximum number of carbon atoms in this chain is not particularly critical and may be selected in accordance with the usual practical limits in the art, say up to about 22-24 carbon atoms, for most purposes.
  • the other substituents onthis nitrogen atom may be hydrogen atoms or short chain hydrocarbon groups with up tozabout five carbon atoms and preferably one or two carbon atoms. Quaternary ammonium derivatives of such'salts may also be useful.
  • Suitable amine salts include salts of amines, for example, higher alkylamines such as primary amines such as mixed amines, for example, coconut oil amines, beef tallow amines and soybean oil amines; secondary amines such as N- dodecylpropylenediamine, N- pentadecylethylenediamine, N-decylhexamethylenediamineand beef tallow propylenediamine; and tertiary amines such as condensate of stearic acid with N-oleyl-N', N'-diethylethylenediamine or triethanolamine and N-acylates of alkylenetriamines, with inorganic acids suchas hydrochloric acid and phosphoric acid or with organic acids such as acetic acid, propionic acid, tertaric acid and succinic acid.
  • higher alkylamines such as primary amines such as mixed amines, for example, coconut oil amines, beef
  • a higher aliphatic or aromatic sulfonate serves as the I other constituent of the flotation reagent in the present invention.
  • These surfactants often referred to as the alkane sulfonates, have a long chain hydrocarbon group, either saturated, unsaturated or mixtures thereof, connected to a sulfonate radical.
  • the hydrocarbon group should contain at least about eight carbon atoms, and preferably at least about l2, up to the usual limits of the art, with an average of about 22-24 carbons being the normal upper limit as a practical matter, although longer chain compounds would not be excluded where available.
  • Compounds of this type having intermediate linkages, such as ester, amide, or either groups, between the long chain group and the sulfonate radical can also be employed.
  • higher aliphatic or aromatic sulfonates or alkane sulfonates are used in the form of their salts of an alkali metal, preferably sodium, but also potassium, lithium and the like.
  • Sulfonates obtained by sulfonation of higher aliphatic or aromatic hydrocarbons such as higher paraffinic and higher olefinic hydrocarbons are preferred, particularly sodium salts of petroleum sulfonic acids obtained by treatment of petroleum with concentrated sulfuric acid.
  • the proportion of the higher aliphatic amine'salt to the higher aliphatic or aromatic sulfonate is in'the range of 5:95-60:40 by weight.
  • flotation reagents are used in the form of a -50 wt. percent solution in water.
  • the flotation reagent resort to hydrofluoric acid as an activating agent is not required.,1t is sufficient to adjust the pH of the flotation medium to the desired acidity according to the practice of the art by means of sulfuric acid.
  • the acidity will be usually a pH of, at least, about 4.5 and preferably 3.5-2.
  • a raw ore is finely divided and then a fraction having a particle size less than about 1 mm is collected and cent of A1 0, and 0.142 percent of Fe O is divided finely and a fraction of a size below 1 190p. is collected and washed with water.
  • 23 parts of l percent aqueous beef tallow amine acetate (Diomin T) so-' lution are mixed with 77 parts of 1 percent aqueous sodium petroleum sulfonate (Aeropromotor No. 825, a
  • a flotator is adjusted to pH 2-3.5 with sulfuric acid.
  • Pulp concentration is about 20-30 wt. percent.
  • An impeller is rotated to effect sufficient foaming and the resulting froth is separated from the tailings.
  • feldspar and quartz i.e., siliceous sand, are obtained as froth and tailings, respectively.
  • the amount of the flotation reagent should be selected depending upon desired-quality of the recovered feldspar and the separation efficiency.
  • the aggregate amount of the flotation reagents used here, on a dry basis, should not exceed about O.l50.2 percent by weight of ore and smaller quantities in the order of 0.05-0.10 may be preferable in accordance with the usual practice of the art regarding weights of foaming agent and collector together.
  • a froth flotation process for separating feldspar from quartz-feldspar sands ore consisting essentially of the steps of subdividing said ore to produce at least a fraction having a particle size less than about 1 mm, collecting said fraction and washing the same with water to effect desliming, introducing the washed fraction at a solid concentration of about 20-30 wt percent into an aqueous flotation medium acidified to a pH of about 23.5 with sulfuric acid in the absence of hydrofluoric acid, said flotation medium containing about 0.05-0.2 percent by weight of a froth-flotation reagent consisting essentially of l) a salt with an inorganic or organic acid of an organic mono-, dior triamine having attached an amino nitrogen atom a long chain aliphatic hydrocarbon group containing, at least about eight carbon atoms and (2) a higher aromatic or aliphatic sulfonate of an alkali metal in a proportion in the range of 5:95-60:40 by weight,
  • each of said amine salt and said sulfonate include a saturated or unsaturated long chain hydrocarbon radical having at least about eight carbon atoms.
  • said flotation reagent is a' mixture of a beef tallow amine acetate and a aromatic sulfonate.

Abstract

An improved process for separating feldspars from feldspathic ores by means of froth flotation wherein a combination of a higher aliphatic amine salt and a higher aliphatic or aromatic sulfonate is used as a flotation reagent, eliminating the necessity for activation with hydrofluoric acid.

Description

United States Patent 1 1 Katayanagi Oct. 29, 1974 [5 FLOTATION SEPARATION OF FELDSPAR 3,214,018 10/1965 ONeal 209/166 [76] Inventor: Akira Katayanagi, No. 11-65, FOREIGN PATENTS OR APPLICATIONS 3'chomea Kltakyushua Japan 738,614 7/1943 Germany 209/166 [22] Filed: Mar. 6, 1972 OTHER PUBLICATIONS 1 1 pp 232,280 Chem Abst. 28956g, 69, 1968.
v Chem. Abst, 155441), 64, 1966. [30] Foreign Application Priority Data Mar. 10, 1971 Japan 46-13301 Primary Examiner-Robert Halper Attorney, Agent, or Firm-Wil1iam J Daniel [52] US. Cl. 209/166 [51] h t. Cl B03d 1/02 57 ABSTRACT [58] Field of Search 209/ 166, 167 An improved process for Separating fe'ldspars from 1561 223511121202;zfigazifiz srstzzzfiz zzsz UNITED STATES PATENTS higher aliphatic or aromatic sulfonate is used as a flo- 2,459,967 1/1949 Schilling 209/166 X tation reagent, eliminating the necessity for activation Giescke a hydrofluoric acid 2,578,790 12/1951 Duke 209/166 2,633,241 3/1953 Banks 209/166 4 Claims, N0 Drawings BACKGROUND OF THE INVENTION of flotation, especially froth flotation. More particularly, the present invention relates to a process for the flotation of feldspars contained in feldspathic ores by ric acid for hydrofluoric acid as the activating agent and effecting the flotation using a combination of a higher aliphatic amine and a higher aliphatic or arousing a combination of a higher aliphatic amine salt and Y a higher aliphatic or aromatic sulfonate as the flotation reagents so that activation with hydrofluoric acid is unnecessary.
2. Summary of the Prior Art Flotation, especially froth flotation, is well known among the general mineral recovery processes like magnetic separation processes in which useful ore constituents are separated by utilizing a difference in the specific gravities of the ore constituents.
In conventional froth flotation, feldspars have been separated from the feldspathic ores in-which they occur generally by pulverizing an me into a proper particle range, classifying the particles according to size, subjecting them to an activation treatment with hydrofluoric acid, admixing them in water together with a collector (for example, an aliphatic amine) and a foaming agent (for example, pine oil), introducing air therein to cause bubbling, and recovering the feldspars in the froth or foam thus generated, leaving other constituents, such as quartz, as tailings. However, the hydrofluoric acid used as the activator in this process reacts violently with other substances due to'its high reactivity. Further, hydrofluoric acid is a highly poisonous reagent and, therefore, must be handled with the greatest possible care. In addition, hydrofluoric acid has the disadvantage of attacking and dissolving the surface of the quartz with a reduction in the yield of the product. Complications are therefore presented in carrying out this process on a commercial scale.
Accordingly, an object of the present invention is to provide an improved process for the flotation, espe cially froth flotation, of feldspars from feldspathic ores.
Another object of the invention is to provide a process for the flotation of feldspar which does not require activation with hydrofluoric acid. I
Still another object of the invention is to provide a novel flotation process for separating feldspars from feldspathic ores wherein a combination of a higher aliphatic amine salt and a higher aliphatic or aromatic sulfonate is used as the flotation reagent under an acidic condition provided by sulfuric acid.
Further objects of the invention will be apparent from the following description.
GENERAL DESCRIPTION OF THE INVENTION dodecylamine, pentadecylamine and octadecylamine;
matic sulfonate-as the'flotation reagent in the separation of feldspars from feldspathic minerals and ores.
The higher aliphatic amine salt used as one component of the flotation reagent in the present invention may be any higheraliphatic amine salt known to have utility as the so-called collector in conventional flotation processes. These salts are cationic surfactants containing at least one amino group and having attached to the nitrogen atomsof one amino group thereof a long chain hydrocarbon group, saturated, unsaturated and mixtures thereof, containing at least about eight carbon atoms and preferably at least about l2 carbons. The maximum number of carbon atoms in this chain is not particularly critical and may be selected in accordance with the usual practical limits in the art, say up to about 22-24 carbon atoms, for most purposes. The other substituents onthis nitrogen atom may be hydrogen atoms or short chain hydrocarbon groups with up tozabout five carbon atoms and preferably one or two carbon atoms. Quaternary ammonium derivatives of such'salts may also be useful.
Examples of suitable amine salts include salts of amines, for example, higher alkylamines such as primary amines such as mixed amines, for example, coconut oil amines, beef tallow amines and soybean oil amines; secondary amines such as N- dodecylpropylenediamine, N- pentadecylethylenediamine, N-decylhexamethylenediamineand beef tallow propylenediamine; and tertiary amines such as condensate of stearic acid with N-oleyl-N', N'-diethylethylenediamine or triethanolamine and N-acylates of alkylenetriamines, with inorganic acids suchas hydrochloric acid and phosphoric acid or with organic acids such as acetic acid, propionic acid, tertaric acid and succinic acid.
A higher aliphatic or aromatic sulfonate serves as the I other constituent of the flotation reagent in the present invention. These surfactants, often referred to as the alkane sulfonates, have a long chain hydrocarbon group, either saturated, unsaturated or mixtures thereof, connected to a sulfonate radical. The hydrocarbon group should contain at least about eight carbon atoms, and preferably at least about l2, up to the usual limits of the art, with an average of about 22-24 carbons being the normal upper limit as a practical matter, although longer chain compounds would not be excluded where available. Compounds of this type having intermediate linkages, such as ester, amide, or either groups, between the long chain group and the sulfonate radical can also be employed. These higher aliphatic or aromatic sulfonates or alkane sulfonates are used in the form of their salts of an alkali metal, preferably sodium, but also potassium, lithium and the like. Sulfonates obtained by sulfonation of higher aliphatic or aromatic hydrocarbons such as higher paraffinic and higher olefinic hydrocarbons are preferred, particularly sodium salts of petroleum sulfonic acids obtained by treatment of petroleum with concentrated sulfuric acid.
In the flotation reagent, the proportion of the higher aliphatic amine'salt to the higher aliphatic or aromatic sulfonate is in'the range of 5:95-60:40 by weight. The
flotation reagents are used in the form of a -50 wt. percent solution in water.
With a combination of the above-described components are the flotation reagent, resort to hydrofluoric acid as an activating agent is not required.,1t is sufficient to adjust the pH of the flotation medium to the desired acidity according to the practice of the art by means of sulfuric acid. The acidity will be usually a pH of, at least, about 4.5 and preferably 3.5-2.
GENERAL DESCRIPTION OF PREFERRED EMBODlMENT A preferred embodiment of the process of the present invention will be illustrated below.
A raw ore is finely divided and then a fraction having a particle size less than about 1 mm is collected and cent of A1 0, and 0.142 percent of Fe O is divided finely and a fraction of a size below 1 190p. is collected and washed with water. Separately, 23 parts of l percent aqueous beef tallow amine acetate (Diomin T) so-' lution are mixed with 77 parts of 1 percent aqueous sodium petroleum sulfonate (Aeropromotor No. 825, a
- product of American Cyanamide Co.) solution to ob- Quantity Separaof re- Composition of Composition of tion agent isolated siisolated rate of (cc/Kg liceous sand feldspar Feldspar ore) A1 0,, Fe,o, SiO, A1 0 F0 0,,
washed thoroughly with water to effect desliming, Thereafter, the water in a flotator is adjusted to pH 2-3.5 with sulfuric acid. Next, there is added a water solution of a mixture of a higher aliphatic amine salt and a higher aliphatic or aromatic sulfonate (5:95-60:40) of a concentration less than percent. Pulp concentration is about 20-30 wt. percent. An impeller is rotated to effect sufficient foaming and the resulting froth is separated from the tailings. Thus, feldspar and quartz, i.e., siliceous sand, are obtained as froth and tailings, respectively. If the amount of the flotation reagent is increased, the resulting feldspar has a reduced content of A1 0 and Fe O although the yield of feldspar itself is increased. Therefore, the amount of the flotation reagent should be selected depending upon desired-quality of the recovered feldspar and the separation efficiency.
in general, the aggregate amount of the flotation reagents used here, on a dry basis, should not exceed about O.l50.2 percent by weight of ore and smaller quantities in the order of 0.05-0.10 may be preferable in accordance with the usual practice of the art regarding weights of foaming agent and collector together.
According to the process of the present invention, safe operation is assured, since hydrofluoric acid is not used and, in addition, an offensive smell peculiar to pine oil is not present since pine oil isnot used as the foaming agent.
The process of the present invention will.be.illustrated by an example which is intended to illustrate but not to limit the scope of the present invention. Unless otherwise stated, all parts and percentages are by weight.
EXAMPLE A raw ore containing 88.71 percent of SiO 9.40 per ii's ipaini'fidni the above Tabld as the quantity of the flotation reagent is increased, the separation rate of the feldspar increases but A1 0 and Fe O content of the separated feldspar froth are reduced.
What is claimed is: t
l. A froth flotation process for separating feldspar from quartz-feldspar sands ore consisting essentially of the steps of subdividing said ore to produce at least a fraction having a particle size less than about 1 mm, collecting said fraction and washing the same with water to effect desliming, introducing the washed fraction at a solid concentration of about 20-30 wt percent into an aqueous flotation medium acidified to a pH of about 23.5 with sulfuric acid in the absence of hydrofluoric acid, said flotation medium containing about 0.05-0.2 percent by weight of a froth-flotation reagent consisting essentially of l) a salt with an inorganic or organic acid of an organic mono-, dior triamine having attached an amino nitrogen atom a long chain aliphatic hydrocarbon group containing, at least about eight carbon atoms and (2) a higher aromatic or aliphatic sulfonate of an alkali metal in a proportion in the range of 5:95-60:40 by weight, agitating said medium to produce a froth containing feldspar, and separating said froth from the medium containing quartz as tailmgs.
2. The process of claim 1 wherein each of said amine salt and said sulfonate include a saturated or unsaturated long chain hydrocarbon radical having at least about eight carbon atoms.
3. The process of claim 2 in which said radical contains at least about 12 carbon atoms.
4. The process of claim 1 wherein said flotation reagent is a' mixture of a beef tallow amine acetate and a aromatic sulfonate.

Claims (4)

1. A FROTH FLOATION PROCESS FOR SPEARATING FELDSPAR FROM QUARTZ-FELDSPAR SANDS ORE CONSISTING ESSENTIALLY OF THE STEPS OF SUBDIVIDING SAID ORE TO PRODUCE AT LEAST A FRACTION HAVING A PARTICLE SIZE LESS THAN ABOUT 1MM, COLLCTING SAID FRACTION AND WASHING THE SAME WITH WATER TO EFFECT DESLIMING, INTRODUCING THE WASHED FRACTION AT A SOLID CONCENTRATION OF ABOUT 20-30 WT PERCENT INTO AN AQUEOUS FLOTATION MEDIUM ACIDIFIED TO A PH OF ABOUT 1-3.5 WITH SULFURIC ACID IN THE ABSENCE OF HYDROFLUORIC ACID, SAID FLOTATION MEDIUM CONTAINING ABOUT 0.05-0.2 PERCENT BY EIGHT OF A FROTH-FLOTATION REAGENT CONSISTING ESSENTIALLY OF (1) A SALT WITH AN INORGANIC OR ORGANIC ACID OF AN ORGANIC MONO, DI- OR TRIAMINE HAVING ATTACHED AN AMINO NITROGEN ATOM A LONG CHAIN ALIPHATIC HYDROCARBON GROUP CONTAINING, AT LEAST ABOUT EIGHT CARBON ATOMS AND (2) A HIGHER AROMATIC OR ALIPHATIC SULFONATE OF AN ALKALI METAL IN A PROPORTION IN THE RANGE OF 5:95-60-40 BY WEIGHT, AGITATING SAID MEDIUM TO PRODUCE A FORTH CONTAINING FELDSPAR, AND SEPARATING SAID FORTH FROM THE MEDIUM CONTAINING QUARTZ AS TAILINGS.
2. The process of claim 1 wherein each of said amine salt and said sulfonate include a saturated or unsaturated long chain hydrocarbon radical having at least about eight carbon atoms.
3. The process of claim 2 in which said radical contains at least about 12 carbon atoms.
4. The process of claim 1 wherein said flotation reagent is a mixture of a beef tallow amine acetate and a aromatic sulfonate.
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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4038179A (en) * 1975-06-02 1977-07-26 Akira Katayanagi Hydrochloric acid flotation process for separating feldspar from siliceous sand
US4725351A (en) * 1986-09-29 1988-02-16 International Minerals & Chemical Corp. Collecting agents for use in the froth flotation of silica-containing ores
US4744892A (en) * 1985-02-27 1988-05-17 Henkel Kommanditgesellschaft Auf Aktien Process for dressing kaolinite by flotation
US5507394A (en) * 1994-05-26 1996-04-16 The University Of British Columbia Aqueous composition useful in ore floatation containing aliphatic amine, extender oil, and emulsifier
US6098810A (en) * 1998-06-26 2000-08-08 Pueblo Process, Llc Flotation process for separating silica from feldspar to form a feed material for making glass
EP2343131A1 (en) 2010-01-08 2011-07-13 Institut National Polytechnique de Lorraine (INPL) Flotation process for recovering feldspar from a feldspar ore
CN105057113A (en) * 2015-08-07 2015-11-18 山东华晟投资有限公司 Method for recycling feldspar from gold flotation tailings through fluoride-free alkali process
CN106378264A (en) * 2016-12-07 2017-02-08 广西大学 Preparation method of potassium feldspar collecting agent

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Publication number Priority date Publication date Assignee Title
DE738614C (en) * 1942-01-03 1943-08-23 Krupp Fried Grusonwerk Ag Process for separating mica and mica-like substances from quartz and other gangue rock by flotation
US2459967A (en) * 1946-02-07 1949-01-25 Minerals Separation North Us Concentration of nonsulfide ores
US2483192A (en) * 1945-11-24 1949-09-27 American Cyanamid Co Froth flotation of iron impurities from feldspar
US2578790A (en) * 1951-05-07 1951-12-18 Minerals Separation North Us Froth flotation of ferruginous impurities from finely divided granite rock
US2633241A (en) * 1951-02-01 1953-03-31 Tennessee Valley Authority Froth flotation of iron-bearing minerals from feldspathic ores
US3214018A (en) * 1962-10-08 1965-10-26 Feldspar Corp Froth flotation of micaceous minerals

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE738614C (en) * 1942-01-03 1943-08-23 Krupp Fried Grusonwerk Ag Process for separating mica and mica-like substances from quartz and other gangue rock by flotation
US2483192A (en) * 1945-11-24 1949-09-27 American Cyanamid Co Froth flotation of iron impurities from feldspar
US2459967A (en) * 1946-02-07 1949-01-25 Minerals Separation North Us Concentration of nonsulfide ores
US2633241A (en) * 1951-02-01 1953-03-31 Tennessee Valley Authority Froth flotation of iron-bearing minerals from feldspathic ores
US2578790A (en) * 1951-05-07 1951-12-18 Minerals Separation North Us Froth flotation of ferruginous impurities from finely divided granite rock
US3214018A (en) * 1962-10-08 1965-10-26 Feldspar Corp Froth flotation of micaceous minerals

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* Cited by examiner, † Cited by third party
Title
Chem Abst. 28956g, 69, 1968. *
Chem. Abst, 15544b, 64, 1966. *

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4038179A (en) * 1975-06-02 1977-07-26 Akira Katayanagi Hydrochloric acid flotation process for separating feldspar from siliceous sand
US4744892A (en) * 1985-02-27 1988-05-17 Henkel Kommanditgesellschaft Auf Aktien Process for dressing kaolinite by flotation
US4725351A (en) * 1986-09-29 1988-02-16 International Minerals & Chemical Corp. Collecting agents for use in the froth flotation of silica-containing ores
US5507394A (en) * 1994-05-26 1996-04-16 The University Of British Columbia Aqueous composition useful in ore floatation containing aliphatic amine, extender oil, and emulsifier
US6098810A (en) * 1998-06-26 2000-08-08 Pueblo Process, Llc Flotation process for separating silica from feldspar to form a feed material for making glass
EP2343131A1 (en) 2010-01-08 2011-07-13 Institut National Polytechnique de Lorraine (INPL) Flotation process for recovering feldspar from a feldspar ore
WO2011083136A1 (en) 2010-01-08 2011-07-14 Institut National Polytechnique De Lorraine (Inpl) Flotation process for recovering feldspar from a feldspar ore
US9675980B2 (en) 2010-01-08 2017-06-13 Imerys Ceramics France Flotation process for recovering feldspar from a feldspar ore
CN105057113A (en) * 2015-08-07 2015-11-18 山东华晟投资有限公司 Method for recycling feldspar from gold flotation tailings through fluoride-free alkali process
CN106378264A (en) * 2016-12-07 2017-02-08 广西大学 Preparation method of potassium feldspar collecting agent
CN106378264B (en) * 2016-12-07 2018-11-27 广西大学 A kind of preparation method of potassium feldspar collecting agent

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AU467898B2 (en) 1973-09-13
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