CA2228052C - Process for conditioning kaolin clays prior to removing impurities - Google Patents
Process for conditioning kaolin clays prior to removing impurities Download PDFInfo
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- CA2228052C CA2228052C CA002228052A CA2228052A CA2228052C CA 2228052 C CA2228052 C CA 2228052C CA 002228052 A CA002228052 A CA 002228052A CA 2228052 A CA2228052 A CA 2228052A CA 2228052 C CA2228052 C CA 2228052C
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C1/00—Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
- C09C1/40—Compounds of aluminium
- C09C1/42—Clays
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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
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B1/00—Conditioning for facilitating separation by altering physical properties of the matter to be treated
- B03B1/04—Conditioning for facilitating separation by altering physical properties of the matter to be treated by additives
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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
- B03B—SEPARATING SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS
- B03B9/00—General arrangement of separating plant, e.g. flow sheets
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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
- B03D1/002—Inorganic compounds
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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
- B03D1/008—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
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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
- B03D1/02—Froth-flotation processes
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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
- B03D1/02—Froth-flotation processes
- B03D1/025—Froth-flotation processes adapted for the flotation of fines
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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
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/005—Dispersants
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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
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/02—Collectors
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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
- B03D2203/00—Specified materials treated by the flotation agents; specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
- B03D2203/10—Potassium ores
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/22—Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
- C01P2006/62—L* (lightness axis)
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
- C01P2006/63—Optical properties, e.g. expressed in CIELAB-values a* (red-green axis)
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/60—Optical properties, e.g. expressed in CIELAB-values
- C01P2006/64—Optical properties, e.g. expressed in CIELAB-values b* (yellow-blue axis)
Abstract
Kaolin clays are conditioned for the removal of colored titaniferous impurities by (A) first mixing the kaolin clay with a collector to condition the impurities, in the absence of a dispersant, but in the presenc e of sufficient water to yield a mixture having a solids content of at least 65 percent by weight and (B) then deflocculating the kaolin clay mixture at a pH of at least 4.0 with a dispersant in amounts sufficient to yield a kalolin clay slurry which is suitable for subsequent processing to remove colored titaniferous impurities.
Description
PROCESS FOR CONDITIONING KAOLIN CLAYS
PRIOR TO REMOVING IMPURITIES
Technical Field This invention relates to a process for conditioning kaolin clays. In a more specific aspect, this invention relates to a process for conditioning kaolin clays prior to removing impurities from such clays. This invention also relates to kaolin clays produced by the process of this invention.
Background of the Invention Kaolin is a naturally occurring, relatively fine, white clay which may be generally described as a hydrated aluminum silicate. After purification and beneficiation, kaolin clay is widely used as a filler and pigment in various materials, such as rubber and resins, and in various coatings, such as paints and coatings for paper.
Crude kaolin clay, as mined, contains various forms of discoloring impurities, two major impurities being anatase (Ti02) and iron oxides. To make the clay more acceptable for use in the paper industry, these impurities must be substantially removed by appropriate techniques.
The production of high brightness clays usually includes at least two processing steps. In a first step, a significant portion of the impurities, mainly anatase, is removed by employing one or more physical separation techniques, such as centrifugation, sedimentation, high gradient magnetic separation, froth flotation and/or selective flocculation. The remaining impurities, mainly iron oxides, are subsequently removed by known techniques, such as chemical leaching.
Froth flotation is regarded as one of the most efficient methods for removing colored impurities from kaolin clay. Typically, clays to be beneficiated by froth flotation are first blunged in the presence of a dispersant and pH modifier and then conditioned with a collector.
The job of the collector is to selectively adsorb to impurities and render them hydrophobic. This part of the process is referred to as conditioning. The conditioned impurities, mainly titanium dioxide in the form of iron-rich anatase, are then removed in a flotation machine via the attachment of the hydrophobic impurities to air bubbles which are injected into the feed slurry or into the flotation pulp.
Two general categories of compounds are reported in the literature as collectors for titaniferous impurities in kaolin clay. Cundy U.S. Patent 3,450,257 discloses the use of fatty acid compounds as collectors, and Yoon & Hilderbrand U.S. Patent 4,629,556 discloses the use of hydroxamate compounds as collectors. Each category of compounds has advantages and disadvantages.
However, conventional flotation processing is adversely affected by the dispersant and pH modifier which tend to disrupt the mechanism by which the collector attaches to the impurities. This and other problems encountered when dispersing (i.e., deflocculating a crude kaolin clay for flotation beneficiation) are discussed in Hunter U.S. Patent 3,410,399.
Therefore, a need exists in the kaolin clay industry for a process which will effectively condition kaolin clays for subsequent removal of impurities, such as in a flotation process.
Summary of the Invention Briefly described, the present invention provides an improved process for conditioning kaolin clays prior to removing impurities from such clays in a subsequent processing step. More specifically, this invention provides an improved process for such conditioning of kaolin clays in which the kaolin clays are first conditioned and then slurried in the presence of a dispersant and optionally a pH modifier.
The present invention provides a process by which, depending upon the starting kaolin clay materials, the removal of colored titaniferous impurities from such clays is either equivalent to or improved over conventional processing to remove such impurities.
' Additionally, the present invention provides a process which utilizes the advantages of the collector to remove impurities but which avoids the disadvantages associated with deflocculating kaolin clays prior to conditioning.
PRIOR TO REMOVING IMPURITIES
Technical Field This invention relates to a process for conditioning kaolin clays. In a more specific aspect, this invention relates to a process for conditioning kaolin clays prior to removing impurities from such clays. This invention also relates to kaolin clays produced by the process of this invention.
Background of the Invention Kaolin is a naturally occurring, relatively fine, white clay which may be generally described as a hydrated aluminum silicate. After purification and beneficiation, kaolin clay is widely used as a filler and pigment in various materials, such as rubber and resins, and in various coatings, such as paints and coatings for paper.
Crude kaolin clay, as mined, contains various forms of discoloring impurities, two major impurities being anatase (Ti02) and iron oxides. To make the clay more acceptable for use in the paper industry, these impurities must be substantially removed by appropriate techniques.
The production of high brightness clays usually includes at least two processing steps. In a first step, a significant portion of the impurities, mainly anatase, is removed by employing one or more physical separation techniques, such as centrifugation, sedimentation, high gradient magnetic separation, froth flotation and/or selective flocculation. The remaining impurities, mainly iron oxides, are subsequently removed by known techniques, such as chemical leaching.
Froth flotation is regarded as one of the most efficient methods for removing colored impurities from kaolin clay. Typically, clays to be beneficiated by froth flotation are first blunged in the presence of a dispersant and pH modifier and then conditioned with a collector.
The job of the collector is to selectively adsorb to impurities and render them hydrophobic. This part of the process is referred to as conditioning. The conditioned impurities, mainly titanium dioxide in the form of iron-rich anatase, are then removed in a flotation machine via the attachment of the hydrophobic impurities to air bubbles which are injected into the feed slurry or into the flotation pulp.
Two general categories of compounds are reported in the literature as collectors for titaniferous impurities in kaolin clay. Cundy U.S. Patent 3,450,257 discloses the use of fatty acid compounds as collectors, and Yoon & Hilderbrand U.S. Patent 4,629,556 discloses the use of hydroxamate compounds as collectors. Each category of compounds has advantages and disadvantages.
However, conventional flotation processing is adversely affected by the dispersant and pH modifier which tend to disrupt the mechanism by which the collector attaches to the impurities. This and other problems encountered when dispersing (i.e., deflocculating a crude kaolin clay for flotation beneficiation) are discussed in Hunter U.S. Patent 3,410,399.
Therefore, a need exists in the kaolin clay industry for a process which will effectively condition kaolin clays for subsequent removal of impurities, such as in a flotation process.
Summary of the Invention Briefly described, the present invention provides an improved process for conditioning kaolin clays prior to removing impurities from such clays in a subsequent processing step. More specifically, this invention provides an improved process for such conditioning of kaolin clays in which the kaolin clays are first conditioned and then slurried in the presence of a dispersant and optionally a pH modifier.
The present invention provides a process by which, depending upon the starting kaolin clay materials, the removal of colored titaniferous impurities from such clays is either equivalent to or improved over conventional processing to remove such impurities.
' Additionally, the present invention provides a process which utilizes the advantages of the collector to remove impurities but which avoids the disadvantages associated with deflocculating kaolin clays prior to conditioning.
The present invention also provides kaolin clays which are effectively conditioned for subsequent removal of impurities.
In addition, the present invention provides a process which can be effectively used to condition many types of kaolin clay, including those clays which require a high concentration of dispersant to achieve deflocculation. Examples of clays which can be conditioned by the process of this invention include the coarse-grained clays of Middle Georgia, the fine-grained clays of East Georgia and similar clays which can be found in Brazil and Australia.
Further, the present invention provides a process in which a wide range of dispersants can be used to deflocculate the kaolin clay, because such dispersants are added after the clay has been conditioned.
Accordingly, this invention seeks to provide an improved process for conditioning kaolin clays.
Another aspect of this invention seeks to provide a process for conditioning kaolin clays prior to removing impurities from such clays in a process such as flotation, sedimentation, centrifugation, high gradient magnetic separation and/or selective flocculation.
Another aspect of this invention seeks to provide a process for conditioning kaolin clays by which the subsequent removal of impurities from such clays is more efficient.
Another aspect of this invention seeks to provide a process for conditioning kaolin clays by which the subsequent removal of impurities from such clays results in an increased clay recovery.
Still another aspect of this invention seeks to provide a process for conditioning kaolin clays in which the clays are first conditioned and then deflocculated with a dispersant and optionally a pH modifier.
Still another aspect of this invention seeks to provide a process for conditioning 5 kaolin clays in which the slurry products have improved low shear and high shear viscosities compared to the starting kaolin clay material.
Yet still another aspect of the present invention seeks to provide kaolin clays which have been conditioned prior to deflocculation.
Yet still another aspect of this invention seeks to provide a process which can be effectively used to condition various types of kaolin clays, including fine-and coarse-grained clays.
Yet still another aspect of this invention seeks to provide a process in which a wide range of dispersants can be used due to conditioning the kaolin clay prior to the addition of a dispersant.
These and other aspects, features and advantages of this invention will become apparent from the following detailed description.
Detailed Description of the Invention In accordance with the present invention, kaolin clays are treated (i.e.
conditioned) with a collector and then deflocculated to enable impurities to be removed in a subsequent processing step. A pH modifier is preferably added with the dispersant, but such addition is optional.
We have discovered that, by conditioning prior to deflocculation, the subsequent removal of colored titaniferous impurities from kaolin clays is more effective. A more effective removal of impurities results in an increased recovery of kaolin clay.
In addition, the present invention provides a process which can be effectively used to condition many types of kaolin clay, including those clays which require a high concentration of dispersant to achieve deflocculation. Examples of clays which can be conditioned by the process of this invention include the coarse-grained clays of Middle Georgia, the fine-grained clays of East Georgia and similar clays which can be found in Brazil and Australia.
Further, the present invention provides a process in which a wide range of dispersants can be used to deflocculate the kaolin clay, because such dispersants are added after the clay has been conditioned.
Accordingly, this invention seeks to provide an improved process for conditioning kaolin clays.
Another aspect of this invention seeks to provide a process for conditioning kaolin clays prior to removing impurities from such clays in a process such as flotation, sedimentation, centrifugation, high gradient magnetic separation and/or selective flocculation.
Another aspect of this invention seeks to provide a process for conditioning kaolin clays by which the subsequent removal of impurities from such clays is more efficient.
Another aspect of this invention seeks to provide a process for conditioning kaolin clays by which the subsequent removal of impurities from such clays results in an increased clay recovery.
Still another aspect of this invention seeks to provide a process for conditioning kaolin clays in which the clays are first conditioned and then deflocculated with a dispersant and optionally a pH modifier.
Still another aspect of this invention seeks to provide a process for conditioning 5 kaolin clays in which the slurry products have improved low shear and high shear viscosities compared to the starting kaolin clay material.
Yet still another aspect of the present invention seeks to provide kaolin clays which have been conditioned prior to deflocculation.
Yet still another aspect of this invention seeks to provide a process which can be effectively used to condition various types of kaolin clays, including fine-and coarse-grained clays.
Yet still another aspect of this invention seeks to provide a process in which a wide range of dispersants can be used due to conditioning the kaolin clay prior to the addition of a dispersant.
These and other aspects, features and advantages of this invention will become apparent from the following detailed description.
Detailed Description of the Invention In accordance with the present invention, kaolin clays are treated (i.e.
conditioned) with a collector and then deflocculated to enable impurities to be removed in a subsequent processing step. A pH modifier is preferably added with the dispersant, but such addition is optional.
We have discovered that, by conditioning prior to deflocculation, the subsequent removal of colored titaniferous impurities from kaolin clays is more effective. A more effective removal of impurities results in an increased recovery of kaolin clay.
As a first step in carrying out the process of this invention, kaolin clay is mixed, in the absence of a dispersant, with a collector to condition the impurities.
The mixing is continued until a substantially homogenous kaolin clay mixture is obtained. In this first step, water (which may be added and/or derived from the kaolin clay) is present in an amount sufficient to yield a kaolin clay mixture having a solids content of at least 65 percent by weight.
As a second or subsequent step in carrying out the process of this invention, the mixture from the first step is deflocculated with a dispersant, preferably with a pH modifier, to yield a kaolin clay slurry product which is suitable for subsequent processing to remove colored titaniferous impurities. A preferred method to remove such impurities is flotation processing as described above.
The mixing in the first step can be accomplished with equipment well known in this industry, including extruders, kneaders and pug mills.
Examples of such equipment are described in Perry's Chemical Engineers' Handbook, 6th Edition (1985), McGraw Hill Book Company, Section 19, pp.14-24. The mixing equipment must be selected in order to mechanically work the kaolin clay and exert sufficient energy to produce a high shear/smearing action between the collector and the colored titaniferous impurities in the clay particles. The mixing equipment must be selected to operate in the absence of a dispersant, so that intimate contact can be obtained between the collector and the clay particle surfaces which have not been contaminated with a dispersant.
In the first step, the kaolin clay is mixed under conditions which insure that the kaolin clay is subjected to an energy level of at least 10 horsepower-hours per ton of dry kaolin clay. However, the kaolin clay must not be subjected to an energy level which will destroy the collector. This maximum energy level must be determined for each type of kaolin clay and/or collector.
As described above, a collector is used in the first step of this invention. For purposes of this invention, the term "collector" will be understood to refer to any chemical which will condition the colored titaniferous impurities to render them susceptible to being removed in a subsequent processing step, such as by attachment to air bubbles in a flotation process.
The collector employed in the first step can be, for example, any collector which is conventionally used in a flotation process. Examples of such collectors are fatty acids (including mixtures thereof) having the general formula:
R-C-OM
in which R is an alkyl, aryl or alkylaryl group having 1-26 carbon atoms, and M is hydrogen, an alkali metal or an alkaline earth metal.
Examples of suitable R groups include methyl, ethyl, butyl, octyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl and hexylphenyl.
Examples of suitable alkali metals are lithium, sodium and potassium.
Examples of suitable alkaline earth metals are magnesium, calcium and barium.
These fatty acid compounds are commercially available, such as from Westvaco Corporation, Chemical Division, Charleston Heights, South Carolina.
The mixing is continued until a substantially homogenous kaolin clay mixture is obtained. In this first step, water (which may be added and/or derived from the kaolin clay) is present in an amount sufficient to yield a kaolin clay mixture having a solids content of at least 65 percent by weight.
As a second or subsequent step in carrying out the process of this invention, the mixture from the first step is deflocculated with a dispersant, preferably with a pH modifier, to yield a kaolin clay slurry product which is suitable for subsequent processing to remove colored titaniferous impurities. A preferred method to remove such impurities is flotation processing as described above.
The mixing in the first step can be accomplished with equipment well known in this industry, including extruders, kneaders and pug mills.
Examples of such equipment are described in Perry's Chemical Engineers' Handbook, 6th Edition (1985), McGraw Hill Book Company, Section 19, pp.14-24. The mixing equipment must be selected in order to mechanically work the kaolin clay and exert sufficient energy to produce a high shear/smearing action between the collector and the colored titaniferous impurities in the clay particles. The mixing equipment must be selected to operate in the absence of a dispersant, so that intimate contact can be obtained between the collector and the clay particle surfaces which have not been contaminated with a dispersant.
In the first step, the kaolin clay is mixed under conditions which insure that the kaolin clay is subjected to an energy level of at least 10 horsepower-hours per ton of dry kaolin clay. However, the kaolin clay must not be subjected to an energy level which will destroy the collector. This maximum energy level must be determined for each type of kaolin clay and/or collector.
As described above, a collector is used in the first step of this invention. For purposes of this invention, the term "collector" will be understood to refer to any chemical which will condition the colored titaniferous impurities to render them susceptible to being removed in a subsequent processing step, such as by attachment to air bubbles in a flotation process.
The collector employed in the first step can be, for example, any collector which is conventionally used in a flotation process. Examples of such collectors are fatty acids (including mixtures thereof) having the general formula:
R-C-OM
in which R is an alkyl, aryl or alkylaryl group having 1-26 carbon atoms, and M is hydrogen, an alkali metal or an alkaline earth metal.
Examples of suitable R groups include methyl, ethyl, butyl, octyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl and hexylphenyl.
Examples of suitable alkali metals are lithium, sodium and potassium.
Examples of suitable alkaline earth metals are magnesium, calcium and barium.
These fatty acid compounds are commercially available, such as from Westvaco Corporation, Chemical Division, Charleston Heights, South Carolina.
An especially preferred fatty acid compound is commercially available from Westvaco Corporation under the trademark Westvaco L-5. This compound is a tall oil, which is a mixture of fatty acid compounds.
Other suitable collectors are hydroxamate compounds (including mixtures thereof) having the general formula:
R'-C-NH
0 OM' in which R' is an alkyl, aryl or alkylaryl group having 4-28 carbon atoms, and M' is hydrogen, an alkali metal or an alkaline earth metal.
Examples of suitable R' groups include butyl, hexyl, octyl, dodecyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl and hexylphenyl.
Examples of suitable alkali metals are lithium, sodium and potassium.
Examples of suitable alkaline earth metals are magnesium, calcium and barium.
These hydroxamate compounds are available commercially, such as from Cytec Industries, Inc., West Paterson, New Jersey.
An especially preferred hydroxamate compound is commercially available from Cytec Industries, Inc. under the trademark S-6493 Mining Reagent. This compound is a mixture of alkyl hydroxamic acids.
The hydroxamate collectors used in the invention can be prepared by conventional methods, such as shown in Yoon & Hilderbrand U.S. Patent 4,629,556;
Wang & Nagaraj U.S. Patent 4,871,466; and Wang &
Nagaraj U.S. Patent 4,929,343.
Examples of hydroxamates which are useful in the process of the invention include potassium butyl hydroxamate, potassium octyl hydroxamate, potassium lauryl hydroxamate, potassium 2-ethylhexyl hydroxamate, potassium oleyl hydroxamate, potassium eicosyl hydroxamate, potassium phenyl hydroxamate, potassium naphthyl hydroxamate, potassium hexylphenyl hydroxamate, and the corresponding salts of sodium and other alkali or alkaline earth metals. The salts can be converted to the corresponding acids by conventional methods known to those skilled in the art.
The collector is preferably mixed with the kaolin clay and water under conditions which permit reaction between the collector and the impurities in the clay in a relatively short time.
The amount of collector mixed with the kaolin clay depends on various factors, such as the amount of impurities present in the clay, the nature of the clay to be processed and the amount of dry clay starting material.
In the second step of this process, a suitable dispersant, such as sodium silicate, a polyacrylate, sodium hexametaphosphate and mixtures thereof, is added to deflocculate the kaolin clay mixture from the first step. Generally, the dispersant will be added in an amount, e.g., 1-20 pounds per ton of dry solids, to produce a well-dispersed product suitable for subsequent processing to remove colored titaniferous impurities.
A pH modifier, such as soda ash, sodium hydroxide, ammonium hydroxide, potassium hydroxide, lithium hydroxide and mixtures thereof is added if needed during the second step to maintain a pH of at least 4Ø
A frothing agent, such as that commercially available from Cytec Industries under the trademark Aerofroth 65, may be added if needed during the second step to assist in the subsequent processing to remove colored titaniferous impurities.
The present invention is further illustrated by the following examples which are illustrative of 5 certain embodiments designed to teach those of ordinary skill in the art how to practice this invention and to represent the best mode contemplated for practicing this invention.
In the following examples, the efficiency of 10 the various collectors in removing titaniferous impurities from kaolin clays by froth flotation will be compared using an index known as the "coefficient of separation"
(C.S.), which was first used as a measure of process performance in kaolin flotation by Wang and Somasundaran; see Fine Particles Processiniz, Vol. 2, Chapter 57, pages 1112-1128 (1980). The C.S. index takes into account not only the amount of impurities removed by the process but also the amount of clay product lost as a result of the process. The mathematical expression used to compute the Coefficient of Separataon is the following:
% Yield of Clay + % Ti02 removed by flotation -100 C. S. = ------------------------------------------------------------in which the % yield of clay represents the weight of kaolin clay recovered in the clay product expressed in terms of percentage of the calculated total weight of kaolinite in the feed and the % Ti ~ removed bv o ti n represents the weight of total Ti02 rejected into the floated tailing expressed in terms of the percentages of the total weight of Ti02 in the feed.
The value of the C.S. index varies theoretically from zero for no separation to 1 for a perfect separation as in the unrealistic case in which all (100 percent) of the impurities are removed from the kaolin with absolutely no loss (100 percent yield) of clay. In the case of kaolin beneficiation by froth flotation, the C.S.
index typically ranges from 0.30 - 0.75.
In this patent application, the C.S. index is used to compare the efficiency of the conventional method (deflocculation followed by conditioning) versus that of the present invention (conditioning followed by deflocculation). For purposes of comparison, the performance is considered different only when the C.S.
indices differ by more than 0.1 units.
An ultimate object of removing titaniferous impurities from kaolin clays is to improve the GE
brightness and color of the processed clays. Those skilled in the art of kaolin beneficiation by froth flotation know that, to achieve GE brightness levels of or in excess of 90.0, the content of titaniferous impurities (as % Ti02) in the final product is not expected to exceed 0.5% for coarse-grained clays or 1.0% for fine-grained clays. One skilled in the art also knows that any attempt to try to reduce the content of impurities in the clay much further may result in an unacceptably large loss in clay yield and only a very marginal gain in brightness.
Examples 1-2 Two samples (Examples 1-2) of coarse-grained kaolin clay from Washington County, Georgia containing approximately 1.5 percent Ti02 and 20.0 percent free moisture are tested for flotation response as follows.
In Example 1 which represents the conventional method, 2000 grams of dry clay equivalent are blunged at 60 percent solids for 6 minutes in a high speed mixer at 6,200 rpm with 3 pounds per ton sodium silicate (active basis) and 3 pounds per ton soda ash. An alkyl hydroxamate collector (S-6493 Mining Reagent) is introduced at the rate of 2 pounds per ton (as received basis), and the slurry is conditioned an additional 6 minutes at 6,200 rpm. The conditioned clay slu is diluted to 25 percent solids and tested in a Denver~ 12 flotation machine operating at 1,800 rpm. Demineralized water is used for blunging/conditioning and flotation to negate the possible effects of heavy metal ions present in tap water. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
In Example 2 which represents the present invention, the order of the blunging and conditioning steps is reversed to allow the introduction of the alkyl hydroxamate prior to deflocculation. This method is as follows: 900 grams of dry clay equivalent, 2 pounds per ton alkyl hydroxamate collector (as used in Example 1), and demineralized water are added to a Readco one quart laboratory mixer and allowed to mix at 74-75 percent solids for 15 minutes. This process is carried out on three 900 gram samples. The mixer is fitted with two sigma type blades rotating at 75 rpm and a lid which prevents the loss of clay and reagents and which assures a high level of contact between the blades and the contents.
2000 grams of this conditioned clay are then deflocculated by blunging at 6,200 rpm at 60 percent solids with 3 pounds per ton sodium silicate and 3 pounds per ton soda ash. The blunged slip is then diluted and tested in the Denver machine. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
The results given in Table 1 indicate that this invention (Example 2) effectively prepares coarse-grained kaolin clay for flotation response. In Example 2, grade, percent yield and the efficiency of Ti02 removal are equivalent to the conventional method (Example 1).
Other suitable collectors are hydroxamate compounds (including mixtures thereof) having the general formula:
R'-C-NH
0 OM' in which R' is an alkyl, aryl or alkylaryl group having 4-28 carbon atoms, and M' is hydrogen, an alkali metal or an alkaline earth metal.
Examples of suitable R' groups include butyl, hexyl, octyl, dodecyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl and hexylphenyl.
Examples of suitable alkali metals are lithium, sodium and potassium.
Examples of suitable alkaline earth metals are magnesium, calcium and barium.
These hydroxamate compounds are available commercially, such as from Cytec Industries, Inc., West Paterson, New Jersey.
An especially preferred hydroxamate compound is commercially available from Cytec Industries, Inc. under the trademark S-6493 Mining Reagent. This compound is a mixture of alkyl hydroxamic acids.
The hydroxamate collectors used in the invention can be prepared by conventional methods, such as shown in Yoon & Hilderbrand U.S. Patent 4,629,556;
Wang & Nagaraj U.S. Patent 4,871,466; and Wang &
Nagaraj U.S. Patent 4,929,343.
Examples of hydroxamates which are useful in the process of the invention include potassium butyl hydroxamate, potassium octyl hydroxamate, potassium lauryl hydroxamate, potassium 2-ethylhexyl hydroxamate, potassium oleyl hydroxamate, potassium eicosyl hydroxamate, potassium phenyl hydroxamate, potassium naphthyl hydroxamate, potassium hexylphenyl hydroxamate, and the corresponding salts of sodium and other alkali or alkaline earth metals. The salts can be converted to the corresponding acids by conventional methods known to those skilled in the art.
The collector is preferably mixed with the kaolin clay and water under conditions which permit reaction between the collector and the impurities in the clay in a relatively short time.
The amount of collector mixed with the kaolin clay depends on various factors, such as the amount of impurities present in the clay, the nature of the clay to be processed and the amount of dry clay starting material.
In the second step of this process, a suitable dispersant, such as sodium silicate, a polyacrylate, sodium hexametaphosphate and mixtures thereof, is added to deflocculate the kaolin clay mixture from the first step. Generally, the dispersant will be added in an amount, e.g., 1-20 pounds per ton of dry solids, to produce a well-dispersed product suitable for subsequent processing to remove colored titaniferous impurities.
A pH modifier, such as soda ash, sodium hydroxide, ammonium hydroxide, potassium hydroxide, lithium hydroxide and mixtures thereof is added if needed during the second step to maintain a pH of at least 4Ø
A frothing agent, such as that commercially available from Cytec Industries under the trademark Aerofroth 65, may be added if needed during the second step to assist in the subsequent processing to remove colored titaniferous impurities.
The present invention is further illustrated by the following examples which are illustrative of 5 certain embodiments designed to teach those of ordinary skill in the art how to practice this invention and to represent the best mode contemplated for practicing this invention.
In the following examples, the efficiency of 10 the various collectors in removing titaniferous impurities from kaolin clays by froth flotation will be compared using an index known as the "coefficient of separation"
(C.S.), which was first used as a measure of process performance in kaolin flotation by Wang and Somasundaran; see Fine Particles Processiniz, Vol. 2, Chapter 57, pages 1112-1128 (1980). The C.S. index takes into account not only the amount of impurities removed by the process but also the amount of clay product lost as a result of the process. The mathematical expression used to compute the Coefficient of Separataon is the following:
% Yield of Clay + % Ti02 removed by flotation -100 C. S. = ------------------------------------------------------------in which the % yield of clay represents the weight of kaolin clay recovered in the clay product expressed in terms of percentage of the calculated total weight of kaolinite in the feed and the % Ti ~ removed bv o ti n represents the weight of total Ti02 rejected into the floated tailing expressed in terms of the percentages of the total weight of Ti02 in the feed.
The value of the C.S. index varies theoretically from zero for no separation to 1 for a perfect separation as in the unrealistic case in which all (100 percent) of the impurities are removed from the kaolin with absolutely no loss (100 percent yield) of clay. In the case of kaolin beneficiation by froth flotation, the C.S.
index typically ranges from 0.30 - 0.75.
In this patent application, the C.S. index is used to compare the efficiency of the conventional method (deflocculation followed by conditioning) versus that of the present invention (conditioning followed by deflocculation). For purposes of comparison, the performance is considered different only when the C.S.
indices differ by more than 0.1 units.
An ultimate object of removing titaniferous impurities from kaolin clays is to improve the GE
brightness and color of the processed clays. Those skilled in the art of kaolin beneficiation by froth flotation know that, to achieve GE brightness levels of or in excess of 90.0, the content of titaniferous impurities (as % Ti02) in the final product is not expected to exceed 0.5% for coarse-grained clays or 1.0% for fine-grained clays. One skilled in the art also knows that any attempt to try to reduce the content of impurities in the clay much further may result in an unacceptably large loss in clay yield and only a very marginal gain in brightness.
Examples 1-2 Two samples (Examples 1-2) of coarse-grained kaolin clay from Washington County, Georgia containing approximately 1.5 percent Ti02 and 20.0 percent free moisture are tested for flotation response as follows.
In Example 1 which represents the conventional method, 2000 grams of dry clay equivalent are blunged at 60 percent solids for 6 minutes in a high speed mixer at 6,200 rpm with 3 pounds per ton sodium silicate (active basis) and 3 pounds per ton soda ash. An alkyl hydroxamate collector (S-6493 Mining Reagent) is introduced at the rate of 2 pounds per ton (as received basis), and the slurry is conditioned an additional 6 minutes at 6,200 rpm. The conditioned clay slu is diluted to 25 percent solids and tested in a Denver~ 12 flotation machine operating at 1,800 rpm. Demineralized water is used for blunging/conditioning and flotation to negate the possible effects of heavy metal ions present in tap water. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
In Example 2 which represents the present invention, the order of the blunging and conditioning steps is reversed to allow the introduction of the alkyl hydroxamate prior to deflocculation. This method is as follows: 900 grams of dry clay equivalent, 2 pounds per ton alkyl hydroxamate collector (as used in Example 1), and demineralized water are added to a Readco one quart laboratory mixer and allowed to mix at 74-75 percent solids for 15 minutes. This process is carried out on three 900 gram samples. The mixer is fitted with two sigma type blades rotating at 75 rpm and a lid which prevents the loss of clay and reagents and which assures a high level of contact between the blades and the contents.
2000 grams of this conditioned clay are then deflocculated by blunging at 6,200 rpm at 60 percent solids with 3 pounds per ton sodium silicate and 3 pounds per ton soda ash. The blunged slip is then diluted and tested in the Denver machine. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
The results given in Table 1 indicate that this invention (Example 2) effectively prepares coarse-grained kaolin clay for flotation response. In Example 2, grade, percent yield and the efficiency of Ti02 removal are equivalent to the conventional method (Example 1).
#/ton pH %Ti02 %Yield Coefficient of removed of clay separation by (b) flotation (a) Example 1 Alkyl Hydroxamate 2 Sodium Silicate 3 8.1 80.0 90.0 0.70 Soda Ash 3 Example 2 Alkyl Hydroxamate 2 Sodium Silicate 3 7.9 76.0 91.3 0.67 Soda Ash 3 (a) %TiO_ removed by flotation: Weight of total Ti02 rejected into the floated tailing expressed in terms of the percentage of the total weight of Ti02 in the feed.
(b) % Yield of clay: Weight of kaolin clay recovered in the clay product expressed in terms of percentage of the calculated total weight of kaolinite in the feed.
Examples 3-4 Two samples (Examples 3-4) of crude fine-grained kaolin clay from East Georgia are used in an 5 amount equivalent to 2000 grams of dry clay in each of two tests.
In Example 3 which represents the conventional method, the clay is first blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence 10 of 9 pounds per ton sodium silicate and 2 pounds per ton soda ash. Four pounds per ton alkyl hydroxamate collector (S-6493 Mining Reagent) are added, and the slurry is conditioned an additional 6 minutes at 6,200 rpm. This conditioned slurry is then diluted with 15 demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. A
portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
In Example 4 which represents the present invention, the clay is mixed at 900 grams dry clay equivalent at 74-75 percent solids in the Readco lab mixer at 75 rpm for 15 minutes in the presence of 4 pounds per ton of the alkyl hydroxamate collector used in Example 3. This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton of sodium hexametaphosphate (SHMP) and 3 pounds per ton soda ash. Clay conditioned and dispersed in this manner is then diluted with demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. A
portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
(b) % Yield of clay: Weight of kaolin clay recovered in the clay product expressed in terms of percentage of the calculated total weight of kaolinite in the feed.
Examples 3-4 Two samples (Examples 3-4) of crude fine-grained kaolin clay from East Georgia are used in an 5 amount equivalent to 2000 grams of dry clay in each of two tests.
In Example 3 which represents the conventional method, the clay is first blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence 10 of 9 pounds per ton sodium silicate and 2 pounds per ton soda ash. Four pounds per ton alkyl hydroxamate collector (S-6493 Mining Reagent) are added, and the slurry is conditioned an additional 6 minutes at 6,200 rpm. This conditioned slurry is then diluted with 15 demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. A
portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
In Example 4 which represents the present invention, the clay is mixed at 900 grams dry clay equivalent at 74-75 percent solids in the Readco lab mixer at 75 rpm for 15 minutes in the presence of 4 pounds per ton of the alkyl hydroxamate collector used in Example 3. This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton of sodium hexametaphosphate (SHMP) and 3 pounds per ton soda ash. Clay conditioned and dispersed in this manner is then diluted with demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. A
portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
#/ton pH %Ti02 %Yield Coefficient of = removed of clay separation by flotation Example 3 Alkyl Hydroxamate 4 Sodium Silicate 9 8.6 60.7 67.3 0.28 Soda Ash 2 Example 4 Alkyl Hydroxamate 4 SHMP 4 8.0 80.0 82.2 0.62 Soda Ash 3 The results given in Table 2 demonstrate the improved effectiveness of this invention when conditioning fine-grained East Georgia clay. This invention provides increased Ti02 removal while increasing the yield of clay.
Examples 5-6 Two samples (Examples 5-6) of crude coarse-grained kaolin clay from Middle Georgia are used in an amount equivalent to 2000 grams of dry clay in each of two tests.
In Example 5 which represents the conventional method, the clay is first blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton sodium hexametaphosphate and 3 pounds per ton soda ash. Two pounds per ton of alkyl hydroxamate collector (S-6493 Mining Reagent) is added, and the slurry is conditioned an additional 6 minutes at 6,200 rpm. This conditioned slurry is then diluted with demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
In Example 6 which represents the present invention, the clay is mixed at 900 grams dry clay equivalent at 74-75 percent solids in the Readco lab mixer at 75 rpm for 15 minutes in the presence of 3.5 pounds per ton of the collector used in Example 5. This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton sodium hexametaphosphate and 3 pounds per ton soda ash. Clay conditioned and dispersed in this manner is then diluted with demineralized water to 25 percent solids and tested on the Denver D- 12 flotation machine at 1,800 rpm. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content.
The results shown in Table 3 indicate that the process of this invention is not affected by the dispersant type. Kaolin clay conditioned in accordance with this invention and then deflocculated with sodium hexametaphosphate, a dispersant known to be problematic in this type of conditioning process - see Hunter U.S. Patent 3,410,399, produces a slurry with excellent grade and recovery. However, a sample prepared in the conventional manner with the same dispersant exhibits no Ti02 removal.
#/ton pH %Ti02 %Yield Coefficient of removed of clay separation by flotation Example 5 Alkyl Hydroxamate 2 SHMP 4 8.2 0.0 N/A 0.00 Soda Ash 4 Example Alkyl Hydroxamate 3.5 SHMP 4 8.0 82.0 90 F 0.72 Soda Ash 4 Examples 7-8 In Example 7, 2000 dry grams of a fine-grained kaolin clay from East Georgia are processed in the conventional manner by first blunging for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 3 pounds per ton sodium silicate and 3 pounds per ton soda ash. Two pounds per ton alkyl hydroxamate collector (S-6493 Mining Reagent) is added, and the slurry is conditioned an additional 6 minutes at 6,200 rpm. This conditioned slurry is then diluted with demineralized water to 25 percent solids and floated on the Denver D-12 flotation machine at 1,800 rpm. A portion is removed for x-ray analysis to determine residual Ti02 content.
Clay beneficiated in this manner is then ozoned for thirty minutes, fractionated to 90 percent <2um equivalent spherical diameter and flocculated by addition of sulfuric acid to pH 3Ø Clay is leached with sodium hydrosulfite at the rate of 9 pounds per ton. Leached clay is filtered, diluted to 20 percent solids, refiltered and then optimally redispersed with the addition of 1 pound per ton soda ash and 3 pounds per ton sodium polyacrylate. The clay is dried and tested for brightness, color and viscosity.
In Example 8, clay from East Georgia is processed according to the present invention by mixing 900 grams dry clay equivalent at 70 percent solids in the Readco lab mixer at 75 rpm for 15 minutes in the presence of 4 pounds per ton alkyl hydroxamate. This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton sodium hexametaphosphate and 4 pounds per ton soda ash. Conditioned and dispersed clay is then diluted with demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. Clay beneficiated in this manner is then ozoned for 30 minutes, fractionated to 90 percent <2um equivalent spherical diameter and flocculated by addition of sulfuric acid to pH 3Ø Clay is leached with sodium hydrosulfite at the rate of 9 pounds per ton. Leached clay is filtered, diluted to 20 percent solids, refiltered and then redispersed with the addition of 2.7 pounds per ton soda ash. Clay is dried and tested for brightness, color and viscosity.
As shown in Table 4, these properties are equal or improved in Example 8, except for Brookfield viscosity. In Example 8, the Brookfield viscosity is higher than in Example 7 because the dispersant system is optimized in Example 7 but not in Example 8.
GE L a b Brookfield Hercules brightness viscosity viscosity (cP) dynes @
1100 rpm Example 7 90.7 96.6 0.24 2.34 250 5 Example 8 91.2 96.4 0.16 1.66 450 5 Examples 9-10 Two samples ( Examples 9-10) of coarse-grained clay from Washington County, Georgia containing approximately 1.5 percent Ti02 and 20.0 percent free moisture and known to be especially high in Brookfield viscosity are tested for flotation response as follows.
In Example 9 which represents the conventional method, 2000 grams of dry clay equivalent are blunged at 60 percent solids for 10 minutes in a high speed mixer at 4,500 rpm with 6 pounds per ton sodium silicate (active basis) and 3 pounds per ton soda ash. An alkyl hydroxamate collector (S-6493 Mining Reagent) is introduced at the rate of 4 pounds per ton (as received basis), and the slurry is conditioned an additional 10 minutes at 4,500 rpm. The conditioned clay is diluted to 25 percent solids, a frothing agent (Aerofroth 65 from Cytec Industries) is added at the rate of 0.2 pounds per ton (as received basis) and the slurry is tested on a Denver D-12 flotation machine operating at 1,500 rpm.
Demineralized water is used for blunging/conditioning and flotation to negate the possible effects of heavy metal ions present in tap water. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980). The floated product is then ozonated for one hour, screened through a 270 mesh screen, and flocculated and leached with 2 pounds per ton alum and 5 pounds per ton sodium hydrosulfite. The leached clay is then filtered and deflocculated in a low shear mixer using a 60 percent/40 percent soda ash/sodium polyacrylate blend to increase the pH to approximately 7Ø The clay is then spray dried, reslurried to 70 percent solids using a Hamilton Beach mixer at low speed, and tested for Brookfield and Hercules viscosities.
In Example 10 which represents the present invention, 900 grams dry clay equivalent is mixed at 74-75 percent solids in a Readco lab mixer at 75 rpm for 15 minutes in the presence of 4 pounds per ton of the hydroxamate collector (S-6493 Mining Reagent). This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 5000 rpm at 60 percent solids in the presence of 6 pounds per ton sodium silicate (active basis) and 3 pounds per ton soda ash. Clay conditioned and dispersed in this manner is then diluted with demineralized water to 25 percent solids, a frothing agent (Aerofroth 65) is added at the rate of 0.2 pounds per ton (as received basis) and the slurry is tested on a Denver D-12 flotation machine operating at 1,500 rpm. Demineralized water is used for blunging/conditioning and flotation to negate the possible effects of heavy metal ions present in tap water. A
portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980). The floated product is then ozonated for one hour, screened through a 270 mesh screen, and flocculated and leached with 2 pounds per ton alum and 5 pounds per ton sodium hydrosulfite. Leached clay is then filtered and deflocculated in a low shear mixer using a 60 percent/40 percent soda ash/sodium polyacrylate blend to increase the pH to approximately 7Ø The clay is then spray drie, d~ reslurried to 70 percent solids using a Hamilton Beach mixer at low speed, and tested for Brookfield and Hercules viscosities.
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Examples 9-10 illustrate the nature of product viscosity improvement which can be achieved with the process of this invention. As shown in Table 5, the present invention (Example 10) produces a product with a better grade, an improved clay recovery and a significantly reduced viscosity.
This invention has been described in detail with particular reference to certain embodiments, but variations and modifications can be made without departing from the spirit and scope of the invention as defmed in the following claims.
In Example 5 which represents the conventional method, the clay is first blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton sodium hexametaphosphate and 3 pounds per ton soda ash. Two pounds per ton of alkyl hydroxamate collector (S-6493 Mining Reagent) is added, and the slurry is conditioned an additional 6 minutes at 6,200 rpm. This conditioned slurry is then diluted with demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980).
In Example 6 which represents the present invention, the clay is mixed at 900 grams dry clay equivalent at 74-75 percent solids in the Readco lab mixer at 75 rpm for 15 minutes in the presence of 3.5 pounds per ton of the collector used in Example 5. This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton sodium hexametaphosphate and 3 pounds per ton soda ash. Clay conditioned and dispersed in this manner is then diluted with demineralized water to 25 percent solids and tested on the Denver D- 12 flotation machine at 1,800 rpm. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion is removed for x-ray analysis to determine residual Ti02 content.
The results shown in Table 3 indicate that the process of this invention is not affected by the dispersant type. Kaolin clay conditioned in accordance with this invention and then deflocculated with sodium hexametaphosphate, a dispersant known to be problematic in this type of conditioning process - see Hunter U.S. Patent 3,410,399, produces a slurry with excellent grade and recovery. However, a sample prepared in the conventional manner with the same dispersant exhibits no Ti02 removal.
#/ton pH %Ti02 %Yield Coefficient of removed of clay separation by flotation Example 5 Alkyl Hydroxamate 2 SHMP 4 8.2 0.0 N/A 0.00 Soda Ash 4 Example Alkyl Hydroxamate 3.5 SHMP 4 8.0 82.0 90 F 0.72 Soda Ash 4 Examples 7-8 In Example 7, 2000 dry grams of a fine-grained kaolin clay from East Georgia are processed in the conventional manner by first blunging for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 3 pounds per ton sodium silicate and 3 pounds per ton soda ash. Two pounds per ton alkyl hydroxamate collector (S-6493 Mining Reagent) is added, and the slurry is conditioned an additional 6 minutes at 6,200 rpm. This conditioned slurry is then diluted with demineralized water to 25 percent solids and floated on the Denver D-12 flotation machine at 1,800 rpm. A portion is removed for x-ray analysis to determine residual Ti02 content.
Clay beneficiated in this manner is then ozoned for thirty minutes, fractionated to 90 percent <2um equivalent spherical diameter and flocculated by addition of sulfuric acid to pH 3Ø Clay is leached with sodium hydrosulfite at the rate of 9 pounds per ton. Leached clay is filtered, diluted to 20 percent solids, refiltered and then optimally redispersed with the addition of 1 pound per ton soda ash and 3 pounds per ton sodium polyacrylate. The clay is dried and tested for brightness, color and viscosity.
In Example 8, clay from East Georgia is processed according to the present invention by mixing 900 grams dry clay equivalent at 70 percent solids in the Readco lab mixer at 75 rpm for 15 minutes in the presence of 4 pounds per ton alkyl hydroxamate. This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 6,200 rpm at 60 percent solids in the presence of 4 pounds per ton sodium hexametaphosphate and 4 pounds per ton soda ash. Conditioned and dispersed clay is then diluted with demineralized water to 25 percent solids and tested on the Denver D-12 flotation machine at 1,800 rpm. Clay beneficiated in this manner is then ozoned for 30 minutes, fractionated to 90 percent <2um equivalent spherical diameter and flocculated by addition of sulfuric acid to pH 3Ø Clay is leached with sodium hydrosulfite at the rate of 9 pounds per ton. Leached clay is filtered, diluted to 20 percent solids, refiltered and then redispersed with the addition of 2.7 pounds per ton soda ash. Clay is dried and tested for brightness, color and viscosity.
As shown in Table 4, these properties are equal or improved in Example 8, except for Brookfield viscosity. In Example 8, the Brookfield viscosity is higher than in Example 7 because the dispersant system is optimized in Example 7 but not in Example 8.
GE L a b Brookfield Hercules brightness viscosity viscosity (cP) dynes @
1100 rpm Example 7 90.7 96.6 0.24 2.34 250 5 Example 8 91.2 96.4 0.16 1.66 450 5 Examples 9-10 Two samples ( Examples 9-10) of coarse-grained clay from Washington County, Georgia containing approximately 1.5 percent Ti02 and 20.0 percent free moisture and known to be especially high in Brookfield viscosity are tested for flotation response as follows.
In Example 9 which represents the conventional method, 2000 grams of dry clay equivalent are blunged at 60 percent solids for 10 minutes in a high speed mixer at 4,500 rpm with 6 pounds per ton sodium silicate (active basis) and 3 pounds per ton soda ash. An alkyl hydroxamate collector (S-6493 Mining Reagent) is introduced at the rate of 4 pounds per ton (as received basis), and the slurry is conditioned an additional 10 minutes at 4,500 rpm. The conditioned clay is diluted to 25 percent solids, a frothing agent (Aerofroth 65 from Cytec Industries) is added at the rate of 0.2 pounds per ton (as received basis) and the slurry is tested on a Denver D-12 flotation machine operating at 1,500 rpm.
Demineralized water is used for blunging/conditioning and flotation to negate the possible effects of heavy metal ions present in tap water. A portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980). The floated product is then ozonated for one hour, screened through a 270 mesh screen, and flocculated and leached with 2 pounds per ton alum and 5 pounds per ton sodium hydrosulfite. The leached clay is then filtered and deflocculated in a low shear mixer using a 60 percent/40 percent soda ash/sodium polyacrylate blend to increase the pH to approximately 7Ø The clay is then spray dried, reslurried to 70 percent solids using a Hamilton Beach mixer at low speed, and tested for Brookfield and Hercules viscosities.
In Example 10 which represents the present invention, 900 grams dry clay equivalent is mixed at 74-75 percent solids in a Readco lab mixer at 75 rpm for 15 minutes in the presence of 4 pounds per ton of the hydroxamate collector (S-6493 Mining Reagent). This process is carried out on three 900 gram samples. From these three samples, a 2000 gram dry clay equivalent sample is taken and blunged for 6 minutes at 5000 rpm at 60 percent solids in the presence of 6 pounds per ton sodium silicate (active basis) and 3 pounds per ton soda ash. Clay conditioned and dispersed in this manner is then diluted with demineralized water to 25 percent solids, a frothing agent (Aerofroth 65) is added at the rate of 0.2 pounds per ton (as received basis) and the slurry is tested on a Denver D-12 flotation machine operating at 1,500 rpm. Demineralized water is used for blunging/conditioning and flotation to negate the possible effects of heavy metal ions present in tap water. A
portion of the beneficiated clay slurry is removed to calculate pulp density from which percent yield is calculated. A second portion of the beneficiated clay slurry is removed for x-ray analysis to determine residual Ti02 content. The percent yield and residual Ti02 are used to calculate the coefficient of separation as described by Wang and Somasundaran (1980). The floated product is then ozonated for one hour, screened through a 270 mesh screen, and flocculated and leached with 2 pounds per ton alum and 5 pounds per ton sodium hydrosulfite. Leached clay is then filtered and deflocculated in a low shear mixer using a 60 percent/40 percent soda ash/sodium polyacrylate blend to increase the pH to approximately 7Ø The clay is then spray drie, d~ reslurried to 70 percent solids using a Hamilton Beach mixer at low speed, and tested for Brookfield and Hercules viscosities.
fi b O N
a O O
El cn p ~t p -~i '> 00 w au ,.., .~
~ O O~ p cn O v~ O
O a p N ~p N
a G~1 > '~.. ~ @J vN-~ ~ @) (U O
U ~+
cz 00 O 4-4 ~ N V ) O cn O O
~
cz (-' O ~
Ql\
~
W W
Examples 9-10 illustrate the nature of product viscosity improvement which can be achieved with the process of this invention. As shown in Table 5, the present invention (Example 10) produces a product with a better grade, an improved clay recovery and a significantly reduced viscosity.
This invention has been described in detail with particular reference to certain embodiments, but variations and modifications can be made without departing from the spirit and scope of the invention as defmed in the following claims.
Claims (30)
1. A process for conditioning kaolin clay prior to removing coloured titaniferous impurities from the kaolin clay, wherein the process comprises the sequential steps of:
A. obtaining a substantially homogeneous mixture by mixing, in the absence of a dispersant, kaolin clay and a collector to condition the impurities, wherein water is present in an amount sufficient to yield a mixture having a solids content of at least 65% by weight;
and B. deflocculating the kaolin clay mixture at a pH of at least 4.0 with a dispersant in an amount sufficient to yield a kaolin clay slurry which is suitable for subsequent processing to remove coloured titaniferous impurities.
A. obtaining a substantially homogeneous mixture by mixing, in the absence of a dispersant, kaolin clay and a collector to condition the impurities, wherein water is present in an amount sufficient to yield a mixture having a solids content of at least 65% by weight;
and B. deflocculating the kaolin clay mixture at a pH of at least 4.0 with a dispersant in an amount sufficient to yield a kaolin clay slurry which is suitable for subsequent processing to remove coloured titaniferous impurities.
2. A process as defined by claim 1 wherein the collector is a fatty acid compound having the general formula:
in which R is an alkyl, aryl or alkylaryl group having 1- 26 carbon atoms and M is hydrogen, an alkali metal or an alkaline earth metal.
in which R is an alkyl, aryl or alkylaryl group having 1- 26 carbon atoms and M is hydrogen, an alkali metal or an alkaline earth metal.
3. A process as defined by claim 2 wherein R is methyl, ethyl, butyl, octyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl or hexylphenyl.
4. A process as defined by claim 2 wherein M is hydrogen, lithium, sodium, potassium, magnesium, calcium or barium.
5. A process as defined by claim 2 wherein the fatty acid compound is a tall oil.
6. A process as defined by claim 1 wherein the collector is a hydroxamate compound having the general formula:
in which R' is an alkyl, aryl or alkylaryl group having 4 - 28 carbon atoms and M' is hydrogen, an alkali metal or an alkaline earth metal.
in which R' is an alkyl, aryl or alkylaryl group having 4 - 28 carbon atoms and M' is hydrogen, an alkali metal or an alkaline earth metal.
7. A process as defined by claim 6 wherein R' is butyl, octyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl or hexylphenyl.
8. A process as defined by claim 6 wherein M' is hydrogen, lithium, sodium, potassium, magnesium, calcium or barium.
9. A process as defined by claim 6 wherein the hydroxamate compound is an alkyl hydroxamate.
10. A process as defined by claim 1 wherein the dispersant is sodium silicate.
11. A process as defined by claim 1 wherein the dispersant is a polyacrylate.
12. A process as defined by claim 1 wherein the dispersant is sodium hexametaphosphate.
13. A process as defined by claim 1 wherein a pH modifier is added in step (B).
14. A process as defined by claim 13 wherein the pH modifier is soda ash, sodium hydroxide, ammonium hydroxide, potassium hydroxide, lithium hydroxide or mixtures thereof.
15. A process as defined by claim 1 wherein a frothing agent is added in step (B).
16. A kaolin clay slurry formed by a process which comprises the sequential steps of:
A. obtaining a homogeneous mixture by mixing, in the absence of a dispersant, kaolin clay and a collector to condition the impurities, wherein water is present in an amount sufficient to yield a mixture having a solids content of at least 65% by weight; and B. deflocculating the kaolin clay mixture at a pH of at least 4.0 with a dispersant in an amount sufficient to yield a kaolin clay slurry which is suitable for subsequent processing to remove coloured titaniferous impurities.
A. obtaining a homogeneous mixture by mixing, in the absence of a dispersant, kaolin clay and a collector to condition the impurities, wherein water is present in an amount sufficient to yield a mixture having a solids content of at least 65% by weight; and B. deflocculating the kaolin clay mixture at a pH of at least 4.0 with a dispersant in an amount sufficient to yield a kaolin clay slurry which is suitable for subsequent processing to remove coloured titaniferous impurities.
17. A kaolin clay slurry as defined by Claim 16 wherein the collector is a fatty acid compound having the general formula:
in which R is an alkyl, aryl or alkylaryl group having 1- 26 carbon atoms and M is hydrogen, an alkali metal or an alkaline earth metal.
in which R is an alkyl, aryl or alkylaryl group having 1- 26 carbon atoms and M is hydrogen, an alkali metal or an alkaline earth metal.
18. A kaolin clay slurry as defined by Claim 17 wherein R is methyl, ethyl, butyl, octyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl or hexylphenyl.
19. A kaolin clay slurry as defined by Claim 17 wherein M is hydrogen, lithium, sodium, potassium, magnesium, calcium or barium.
20. A kaolin clay slurry as defined by Claim 17 wherein the fatty acid compound is a tall oil.
21. A kaolin clay slurry as defined by Claim 16 wherein the collector is a hydroxamate compound having the general formula:
in which R' is an alkyl, aryl or alkylaryl group having 4 - 28 carbon atoms and M' is hydrogen, an alkali metal or an alkaline earth metal.
in which R' is an alkyl, aryl or alkylaryl group having 4 - 28 carbon atoms and M' is hydrogen, an alkali metal or an alkaline earth metal.
22. A kaolin clay slurry as defined by claim 21 wherein R' is butyl, octyl, lauryl, 2-ethylhexyl, oleyl, eicosyl, phenyl, tolyl, naphthyl or hexylphenyl.
23. A kaolin clay slurry as defined by claim 21 wherein M' is hydrogen, lithium, sodium, potassium, magnesium, calcium or barium.
24. A kaolin clay slurry as defined by claim 21 wherein the hydroxamate compound is an alkyl hydroxamate.
25. A kaolin clay slurry as defined by claim 16 wherein the dispersant is sodium silicate.
26. A kaolin clay slurry as defined by claim 16 wherein the dispersant is a polyacrylate.
27. A kaolin clay slurry as defined by claim 16 wherein the dispersant is sodium hexametaphosphate.
28. A kaolin clay slurry as defined by claim 16 wherein a pH modifier is added in step (B).
29. A kaolin clay slurry as defined by claim 28 wherein the pH modifier is soda ash, sodium hydroxide, ammonium hydroxide, potassium hydroxide, lithium hydroxide or mixtures thereof.
30. A kaolin clay slurry as defined by claim 16 wherein a frothing agent is added in step (B).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/509,506 | 1995-07-28 | ||
| US08/509,506 US5685899A (en) | 1995-07-28 | 1995-07-28 | Process for conditioning kaolin clays prior to removing impurities |
| PCT/US1996/012264 WO1997005078A1 (en) | 1995-07-28 | 1996-07-25 | Process for conditioning kaolin clays prior to removing impurities |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2228052A1 CA2228052A1 (en) | 1997-02-13 |
| CA2228052C true CA2228052C (en) | 2008-03-18 |
Family
ID=24026883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002228052A Expired - Lifetime CA2228052C (en) | 1995-07-28 | 1996-07-25 | Process for conditioning kaolin clays prior to removing impurities |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US5685899A (en) |
| AU (1) | AU712629B2 (en) |
| BR (1) | BR9609972A (en) |
| CA (1) | CA2228052C (en) |
| WO (1) | WO1997005078A1 (en) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5830818A (en) * | 1997-04-23 | 1998-11-03 | Thiele Kaolin Company | Process for the microwave beneficiation of discolored kaolin clay materials |
| BR9909117A (en) * | 1998-03-27 | 2000-12-19 | Cytec Tech Corp | Process for removing colored clay impurities |
| US6200377B1 (en) | 1999-04-16 | 2001-03-13 | Thiele Kaolin Company | Process for beneficiation of mixtures of mineral particles |
| US6156284A (en) * | 1999-05-07 | 2000-12-05 | Hurst; Vernon J. | Processing procedure for transforming previously unusable clays and kaolin clays to low viscosity pigment |
| US7132786B1 (en) | 1999-07-23 | 2006-11-07 | Osram Gmbh | Luminescent array, wavelength-converting sealing material and light source |
| US6378703B1 (en) * | 2000-11-30 | 2002-04-30 | Engelhard Corporation | Flotation method for removing colored impurities from kaolin clay |
| CN1311911C (en) * | 2001-07-27 | 2007-04-25 | 奥斯麦特有限公司 | Hydroxamate composition and method for froth fcoatation |
| US7122080B2 (en) * | 2001-09-14 | 2006-10-17 | Imerys Pigments, Inc. | Integrated process for simultaneous beneficiation, leaching, and dewatering of kaolin clay suspension |
| US20080267851A1 (en) * | 2003-08-11 | 2008-10-30 | Sare Edward J | High Whiteness Metakaolin and High Whiteness Fully Calcined Kaolin |
| US7727324B2 (en) * | 2004-05-03 | 2010-06-01 | Imerys Pigments, Inc. | Compositions comprising kaolin having nanosize dimensions |
| US7393462B2 (en) * | 2004-05-13 | 2008-07-01 | Cytec Technology Corp. | Process and reagent for separating finely divided titaniferrous impurities from Kaolin |
| US7406744B2 (en) * | 2005-01-20 | 2008-08-05 | Marc Bruneau | Central vacuum system with secondary airflow path |
| US7780779B2 (en) * | 2005-02-23 | 2010-08-24 | Imerys Pigments, Inc. | Method for separating mixture of finely divided minerals |
| US20060249270A1 (en) * | 2005-05-03 | 2006-11-09 | Alves Paula R | Compositions comprising fine sedimentary kaolin and methods for preparing same |
| US8083848B2 (en) | 2005-05-03 | 2011-12-27 | Imerys Pigments, Inc. | Compositions comprising fine sedimentary kaolin and methods for preparing same |
| ITMI20051187A1 (en) | 2005-06-23 | 2006-12-24 | Esposito Servizi Ecologici S R | PLANT AND PROCESS FOR THE RECYCLING OF WASTE COMING FROM SWEEPING ROADS WATER AND SIMILAR WASHER |
| WO2010080453A2 (en) * | 2008-12-18 | 2010-07-15 | Basf Corporation | Methods for stabilizing hydrous kaolin |
| AU2012318528A1 (en) | 2011-10-07 | 2014-05-22 | Boral Ip Holdings (Australia) Pty Limited | Inorganic polymer/organic polymer composites and methods of making same |
| US8864901B2 (en) | 2011-11-30 | 2014-10-21 | Boral Ip Holdings (Australia) Pty Limited | Calcium sulfoaluminate cement-containing inorganic polymer compositions and methods of making same |
| US8967383B1 (en) * | 2012-10-19 | 2015-03-03 | KaMin, LLC | Processes for producing high-brightness kaolin in high yields, and kaolin materials produced therefrom |
| WO2020068915A1 (en) * | 2018-09-25 | 2020-04-02 | University Of Florida Research Foundation, Inc. | Dye-containing kaolin compositions for crop protection and improving plant physiology |
| CN109305817A (en) * | 2018-10-29 | 2019-02-05 | 江西省欧陶科技有限公司 | A kind of ceramics degumming agent and preparation method thereof |
| CN109847947B (en) * | 2019-01-31 | 2020-08-18 | 东北大学 | Method for flotation decalcification of magnesite by EGTA and SHMP synergistic inhibition |
| CN110947520A (en) * | 2019-10-28 | 2020-04-03 | 中国地质科学院矿产综合利用研究所 | Collecting agent for reverse flotation of medium-low grade collophanite, preparation method and application |
| CN111151381B (en) * | 2020-01-08 | 2021-09-24 | 江西科技师范大学 | Preparation method and application of collecting agent for fine lepidolite flotation |
| CN113845122A (en) * | 2021-11-03 | 2021-12-28 | 山西金宇科林科技有限公司 | Coal series kaolin heavy metal lead removal process |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1103585A (en) * | 1964-03-02 | 1968-02-14 | English Clays Lovering Pochin | Improvements in or relating to the processing of clay |
| US3410399A (en) * | 1966-12-14 | 1968-11-12 | Engelhard Min & Chem | Method for dispersing clay |
| US3827556A (en) * | 1972-11-06 | 1974-08-06 | Engelhard Min & Chem | Purification of kaolin clay by froth flotation |
| US4419228A (en) * | 1980-08-25 | 1983-12-06 | Anglo-American Clays Corporation | Process for producing high brightness clays utilizing magnetic beneficiation and calcining |
| US4483624A (en) * | 1982-08-25 | 1984-11-20 | Freeport Kaolin Company | High intensity conditioning mill and method |
| US4492628A (en) * | 1982-08-25 | 1985-01-08 | Freeport Kaolin Company | Method of treating clay to improve its whiteness |
| US4518491A (en) * | 1982-09-13 | 1985-05-21 | Anglo-American Clays Corporation | Beneficiation of clays by froth flotation |
| US4629556A (en) * | 1984-11-29 | 1986-12-16 | Thiele Kaolin Company | Purification of kaolin clay by froth flotation using hydroxamate collectors |
| US4871466A (en) * | 1987-10-15 | 1989-10-03 | American Cyanamid Company | Novel collectors and processes for making and using same |
| US4929343A (en) * | 1987-10-15 | 1990-05-29 | American Cyanamid Company | Novel collectors and processes for making and using same |
| EP0591406A1 (en) * | 1991-07-03 | 1994-04-13 | Engelhard Corporation | Selective separation of finely-divided minerals by addition of selective collector reagent and centrifugation |
| US5223463A (en) * | 1991-08-01 | 1993-06-29 | Ecc International Inc. | Process for producing a kaolin clay product |
-
1995
- 1995-07-28 US US08/509,506 patent/US5685899A/en not_active Expired - Lifetime
-
1996
- 1996-07-25 CA CA002228052A patent/CA2228052C/en not_active Expired - Lifetime
- 1996-07-25 AU AU65998/96A patent/AU712629B2/en not_active Expired
- 1996-07-25 BR BR9609972A patent/BR9609972A/en not_active Application Discontinuation
- 1996-07-25 WO PCT/US1996/012264 patent/WO1997005078A1/en active Application Filing
-
1997
- 1997-11-10 US US08/967,070 patent/US6007618A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU712629B2 (en) | 1999-11-11 |
| CA2228052A1 (en) | 1997-02-13 |
| US5685899A (en) | 1997-11-11 |
| BR9609972A (en) | 1999-01-12 |
| WO1997005078A1 (en) | 1997-02-13 |
| US6007618A (en) | 1999-12-28 |
| AU6599896A (en) | 1997-02-26 |
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