US20030085012A1 - Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness - Google Patents
Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness Download PDFInfo
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- US20030085012A1 US20030085012A1 US10/233,599 US23359902A US2003085012A1 US 20030085012 A1 US20030085012 A1 US 20030085012A1 US 23359902 A US23359902 A US 23359902A US 2003085012 A1 US2003085012 A1 US 2003085012A1
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- kaolin
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/63—Inorganic compounds
- D21H17/67—Water-insoluble compounds, e.g. fillers, pigments
- D21H17/68—Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays
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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
- C09C1/0015—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings
- C09C1/0018—Pigments exhibiting interference colours, e.g. transparent platelets of appropriate thinness or flaky substrates, e.g. mica, bearing appropriate thin transparent coatings uncoated and unlayered plate-like particles
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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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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/40—Coatings with pigments characterised by the pigments siliceous, e.g. clays
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/54—Particles characterised by their aspect ratio, i.e. the ratio of sizes in the longest to the shortest dimension
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
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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
Definitions
- the present invention relates to a hydrous kaolin, which provides improved optical properties when used as a filler or coating. Also, the present invention relates to a paper coating and a coated paper product that exhibits improved properties, such as improved brightness. Further, the present invention relates to methods for preparing hydrous kaolin products.
- Kaolin clay also referred to as China Clay, or hydrous kaolin, is comprised predominantly of the mineral kaolinite, a hydrous aluminum silicate, together with small amounts of a variety of impurities.
- Particulate kaolins generally exist in three forms: hydrous kaolin, calcined kaolin and chemically aggregated kaolin.
- Hydrous kaolin is primarily the mineral kaolinite, which has been mined and beneficiated from natural sources. Calcined kaolins are obtained by processing hydrous kaolin at high temperatures, e.g., greater than 500° C.
- Chemically aggregated kaolins are particle aggregates having a microstructure resembling that of calcined kaolins produced by treating hydrous kaolin with chemicals. Calcined and chemically aggregated kaolins can show benefits in certain application compositions when compared with hydrous kaolins.
- calcined and chemically aggregated kaolins are not without disadvantages.
- the manufacturing costs of calcined and chemically aggregated kaolins are significantly higher than those of hydrous kaolins.
- the calcined and chemically aggregated kaolins also have the effect of improving certain paper properties while adversely effecting other properties, e.g., strength.
- Kaolin has been used as an extender or pigment in paints, plastics and paper coating compositions.
- Kaolin pigments confer desirable physical and optical properties to such compositions.
- flattening (or matting) agents they help smooth the surfaces of the substrates to which they are applied.
- opacifiers they impart brightness, whiteness, gloss and other desirable optical properties.
- extenders they allow partial replacement of titanium dioxide and other more expensive pigments with minimal loss of whiteness or brightness.
- Paper coatings are applied to sheet materials for a number of purposes including, but not limited to, increasing the gloss, smoothness, opacity and/or brightness of the material. Coatings may also be applied to hide surface irregularities or in other ways improve the surface for the acceptance of print. Paper coatings are generally prepared by forming a fluid aqueous suspension of pigment material together with a hydrophilic adhesive and other optional ingredients.
- Coatings have been conventionally applied by means of a coating machine including a short dwell time coating head, which is a device in which a captive pond of coating composition under a slightly elevated pressure is held in contact with a moving paper web for a time sufficient to coat the paper before excess coating composition is removed by means of a trailing blade.
- a short dwell time coating head which is a device in which a captive pond of coating composition under a slightly elevated pressure is held in contact with a moving paper web for a time sufficient to coat the paper before excess coating composition is removed by means of a trailing blade.
- FIG. 1 is a flowchart illustrating a process for refining a coarse fraction kaolin according to Example 1;
- FIG. 2 is a flowchart illustrating a process for refining a coarse fraction kaolin according to Example 2;
- FIG. 3 is a flowchart illustrating a process for refining a coarse fraction kaolin according to Example 3;
- FIG. 4 is a flowchart illustrating the process for making a barrier coating pigment from a coarse fraction kaolin
- FIG. 5 is a graph illustrating brightness (y-axis) as a function of the TiO 2 content (x-axis) for two paper coatings according to the present invention
- FIG. 6 is a graph illustrating sheen (y-axis) versus opacity (x-axis) of various ground U.S. clays;
- FIG. 7 illustrates a plot of the d50 (y-axis) versus shape factor (x-axis) for Invention Kaolin 3 and Invention Kaolin 4 compared to two prior art kaolins;
- FIG. 8 is a flowchart illustrating a process for refining a coarse fraction kaolin according to Example 10.
- kaolins used in coatings and fillers are selected to have a narrow particle size distribution and high crystallinity which have been believed to provide the favored set of physical and optical properties, for example, maximum light scatter.
- coarse kaolin clays have been recognized as exhibiting poor light scatter.
- the present invention differs from the prior art in providing a coating or filling composition including a kaolin that may be rather coarse, but which nonetheless exhibits high light scatter.
- the kaolins according to the present invention showed a light scatter similar to calcined clays without the detrimental effects on strength associated with calcined clays.
- the compositions according to the present invention further improve over prior compositions by making it possible to maintain sheet brightness while further reducing the amount of expensive TiO 2 present in the paper coating composition.
- a paper coating composition comprising at least one kaolin having a shape factor of at least about 70:1, a TiO 2 , a binder, and optionally a dispersant, and wherein the paper coating composition has a ratio of the kaolin to TiO 2 of less than about 85:15 parts by weight.
- a method of making a coated paper comprising coating a fibrous substrate with a paper coating composition comprising a binder and at least one kaolin having a shape factor of at least about 70:1.
- coated paper comprising a fibrous substrate and a paper coating composition comprising kaolin having a shape factor of at least about 70:1.
- a method of improving barrier properties in paper comprising coating a fibrous substrate with a coating composition comprising kaolin having a shape factor of at least about 70:1.
- One aspect of the present invention provides a composition comprising kaolin having a shape factor of at least about 70:1.
- the kaolin can have a shape factor of at least about 80:1, at least about 90:1, or at least about 100:1.
- Another aspect of the present invention provides a coating composition, comprising kaolin having a shape factor of at least about 70:1, a binder; and optionally a dispersant.
- Another aspect of the present invention provides a filler comprising kaolin having a shape factor of at least about 70:1.
- Another aspect of the present invention provides a method of making a coated paper comprising coating a fibrous substrate with a paper coating composition comprising a carrier and kaolin having a shape factor of at least about 70:1.
- Another aspect of the present invention provides a method of making a filled paper comprising providing a fibrous substrate, and adding to the substrate kaolin having a shape factor of at least about 70:1.
- Another aspect of the present invention provides a coated paper comprising a fibrous substrate and a coating on the substrate comprising kaolin having a shape factor of at least about 70:1.
- Another aspect of the present invention provides a method of improving barrier properties in paper comprising coating a fibrous substrate with a coating composition comprising kaolin having a shape factor of at least about 70:1.
- Another aspect of the present invention provides a method of refining kaolin, comprising providing a kaolin slurry, attrition grinding the kaolin slurry, removing the coarse particle size fraction from the slurry by centrifugation, and attrition grinding the coarse-particle size fraction to provide a kaolin product having a shape factor of at least about 70:1.
- Another aspect of the present invention provides an extender for paint comprising kaolin, prepared by a method comprising providing a kaolin slurry comprising whole crude kaolin or a blend of whole crude and coarse-particle size fractions from a centrifuge, attrition grinding the kaolin slurry, removing the coarse particle size fraction from the slurry by centrifugation, and attrition grinding the coarse-particle size fraction to provide a kaolin product having a shape factor of at least about 70:1.
- Another aspect of the present invention provides a slurry comprising kaolin having a shape factor of greater than 70:1 and a stabilizing agent.
- One aspect of the present invention provides a composition that is used in the production of coated or filled substrates.
- Another aspect of the present invention provides the coated or filled products made according to the present invention.
- the compositions and products according to the present invention utilize kaolin having a high shape factor to prepare a coated or filled paper exhibiting improved brightness.
- Shape factor as used herein is a measure of an average value (on a weight average basis) of the ratio of mean particle diameter to particle thickness for a population of particles of varying size and shape as measured using the electrical conductivity method and apparatus described in U.S. Pat. No. 5,128,606, which is incorporated herein by reference in its entirety. In the measurement method described in U.S. Pat. No.
- the electrical conductivity of a fully dispersed aqueous suspension of the particles under test is caused to flow through an elongate tube. Measurements of the electrical conductivity are taken between (a) a pair of electrodes separated from one another along the longitudinal axis of the tube, and (b) a pair of electrodes separated from one another across the transverse width of the tube, and using the difference between the two conductivity measurements the shape factor of the particulate material under test is determined.
- “Hyperplaty” refers to hydrous kaolin clays with shape factors of greater than about 40:1. In one embodiment according to the present invention, the kaolin clays have shape factors of greater than about 70:1, for example greater than about 80:1, or greater than about 90:1.
- the shape factor is greater than about 100:1, for example 110:1 and above.
- the kaolin clay has a shape factor of at and above about 120:1 and at and above about 140:1. The clays according to these embodiments of the invention have been found to show surprisingly high light scatter in paper coatings and fillings.
- the high shape factor may be achieved by grinding mined kaolinitic clays until the desired shape factor is achieved. Any art recognized grinding method can be used with the present invention including but not limited to, for example, wet grinding using sand or ceramic media.
- the kaolin may be prepared by light comminution, e.g., grinding or milling, of a coarse kaolin to give suitable delamination thereof.
- the comminution may be carried out by use of beads or granules of a ceramic or plastic, e.g., nylon, grinding or milling aid.
- Appropriate grinding energies will be readily apparent and easily calculated by the skilled artisan. Significant grinding energies may be necessary to attain desirable high shape factors, however kaolin crude selected for its natural platyness will grind to high shape factors in an energy range typically used to manufacture standard delaminated kaolin pigments that have lesser shape factors.
- Crude kaolin or a high shape factor product obtained from grinding or milling may be refined to remove impurities and improve physical properties using well known procedures generally referred to as beneficiation processes.
- the kaolin may be treated by a known particle size classification procedure, screening and/or centrifuging, to obtain particles having a desired particle size distribution and d 50 value (as discussed below).
- mined clays are suitably first degritted before they are subjected to grinding to achieve the desired shape factor.
- mean particle diameter is defined as the diameter of a circle that has the same area as the largest face of the particle.
- the mean particle size, d 50 value, and other particle size properties referred to in the present application are measured in a well known manner by sedimentation of the particulate material in a fully dispersed condition in an aqueous medium using a SEDIGRAPH 5100 machine as supplied by Micromeritics Corporation. Such a machine provides measurements and a plot of the cumulative percentage by weight of particles having a size, referred to in the art as the “equivalent spherical diameter” (esd), less than the given esd values.
- the mean particle size d 50 is the value determined in this way of the particle esd at which there are 50% by weight of the particles, which have an esd less than that d 50 value.
- d 50 for the particulate kaolin according to the present invention may be, for example, in the range of about 0.2 ⁇ m to about 10 ⁇ m.
- the particle size distribution of the kaolin may be such that about 20% or more of the particles have an esd of 2 microns or less.
- a suitable product according to the invention may have a particle size distribution where about 50% to about 85% of the particles have an esd of 2 microns or less.
- the steepness of the particle size distribution (psd) of the particulate kaolin according to the present invention refers to the slope of the psd curve.
- the psd of the kaolin according to the present invention may be steep and in other cases it may be broad.
- the steepness or broadness of the psd is one indicator of anticipated product performance and can be selected by the skilled artisan based upon desired end properties.
- Steepness is measured as 100 times the ratio of d 30 to d 70 , where d 30 is the value of the particle esd less than which there are 30% of the particles and d 70 is the value of the particle esd less than which there are 70% of the particles as obtained from the psd measure above.
- Kaolin consists predominantly of kaolinite crystals, which are shaped as thin hexagonal plates or in booklets of platelets called “stacks.” Kaolinite stacks may be subjected to a grinding action to easily separate or delaminate the stacks or books comprised of more than one platelet into smaller books or individual platelets.
- delamination parts cleaves natural kaolinite crystals along the (001) crystallographic plane that is perpendicular to its “c-axis.”
- Many standard kaolin products are made by attrition grinding a dispersed slurry of blunged-degritted-brightness beneficiated blend of whole crude and coarse-particle size fraction from a centrifuge. These standard delaminated products, however, may not show sufficient delamination, as they can contain booklets that comprise several to scores of kaolinite platelets.
- this aspect of the present invention provides a method for obtaining a kaolin having a shape factor of about 70:1 or higher.
- the method comprises: (a) providing a kaolin slurry, where in one embodiment, the slurry comprises a whole crude kaolin or a blend of whole crude and coarse particle kaolin from a centrifuge; (b) attrition grinding the kaolin slurry; (c) removing a coarse particle size fraction from the slurry by centrifugation; and (d) attrition grinding the coarse-particle size fraction.
- a centrifugation step may be inserted prior to (b) to remove ultrafine particles in order to enhance the efficiency of attrition grinding.
- the kaolin product is produced by attrition grinding a crude clay slurry.
- the crude can comprise, in one embodiment, either a whole crude or a blend of whole crude and coarse-particle size fractions from a centrifuge.
- the clay slurry may be a dispersed-degritted-brightness beneficiated clay slurry.
- the kaolin slurry can be obtained from crude kaolin ore, which is generally a viscous, sedimentary kaolin containing micas, mixed-layered clay minerals, smectites, and vermiculites or hydrous micas.
- An exemplary kaolin clay crude further comprises potassium oxide in an amount ranging from 0.10% to 3.0% by weight, and magnesium oxide in an amount ranging from 0.03% to 0.5% by weight.
- Such crude can have a shape factor equal to or greater than 15, or equal to or greater than 25.
- the crude kaolin can have a particle size distribution of 75% by weight less than 2 ⁇ m.
- kaolin slurry water can be added to a dry kaolin crude to form an aqueous suspension, such as a suspension containing from 30% to 70% kaolin on a dry weight basis. Chemicals can be added to disperse the clay particles. The kaolin slurry can then be degritted to remove sand-sized particles prior to further processing or transport by pipeline to a plant.
- aqueous suspension such as a suspension containing from 30% to 70% kaolin on a dry weight basis.
- Chemicals can be added to disperse the clay particles.
- the kaolin slurry can then be degritted to remove sand-sized particles prior to further processing or transport by pipeline to a plant.
- the coarse particle size fraction may have a shape factor of greater than 20, such as a shape factor greater than 25. In another embodiment, the coarse particle size fraction may have a shape factor of greater than 35.
- the attrition grinding steps can be performed with a particulate grinding medium for a time sufficient to dissipate in the slurry or suspension enough energy to impart the kaolin particles with a shape factor value ranging from about 35 to about 60 or greater.
- the attrition grinding the crude kaolin slurry results in kaolin having a shape factor value of at least about 60.
- the amount of energy dissipated in the suspension of kaolin clay can range from about 20 kWh to about 100 kWh, such as from about 25 to about 75 kWh of energy per ton of kaolin present on a dry weight basis.
- the attrition grinding mill is equipped with a stirrer, which is capable of being rotated at a speed such that a vortex is formed in the suspension in the mill during grinding.
- the particulate grinding medium can have a specific gravity of 2 or more.
- the grinding medium comprises grains of quartz sand, or similar media.
- the grains can have a diameter of less than 2 mm.
- the grains have a diameter of greater than 0.25 mm and less than 2 mm.
- the grinding medium comprises fine (20-40#) Carbolite media.
- the slurry Prior to attrition grinding the crude kaolin slurry, the slurry can be subjected to beneficiation and/or degritting processes.
- the crude kaolin slurry comprises a dispersed-degritted-brightness beneficiated clay slurry.
- Degritting is the process of passing a kaolin clay slurry through drag boxes and a screen to remove coarse (grit) particles of a given size.
- the screen can be a +325 mesh (U.S. Standard) screen suitable for removing particles larger than 45 ⁇ m.
- the slurry can be passed through a centrifuge, such as a solid-bowl decanter centrifuge, for a classification step, where the clay is classified to a particle size distribution such that 80% to 95% by weight of the particles have an esd less than 2 ⁇ m. In one embodiment, 85% to 92% by weight of the particles have an esd less than 2 ⁇ m. In yet another embodiment, 20% to 40% of the particles have an esd less than 0.25 ⁇ m. In still another embodiment, 25% to 35% of the particles have an esd less than 0.25 ⁇ m. In still another embodiment, the weight of the particles in the finer fraction ranges from 5% to 30% of the feed to centrifuge.
- a centrifuge such as a solid-bowl decanter centrifuge
- the coarse-fraction can be diluted with water to form a slurry that may be subjected to an additional attrition grinding step to produce the final kaolin product having a shape factor value of at least 70.
- This product may alternatively subject to further beneficiation to obtain desired brightness or rheology through conventional processing techniques such as flotation, selective flocculation, and bleaching.
- coarse fractions were discarded, as this kaolin fraction was sometimes regarded as being too coarse for coating applications.
- one advantage of this embodiment arises from the use of coarse fraction, which was in some cases a previously undesired manufacturing by-product, to produce a useful, kaolin product.
- the coarse particle size fraction comprises kaolin having a shape factor of at least about 20, such as at least about 25 or at least about 30, and in some cases as high as about 50 to about 60.
- the final kaolin particles can have a mean particle size (d 50 by Sedigraph) ranging from about 0.1 ⁇ m to about 2.0 ⁇ m, such as a d 50 ranging from about 0.25 ⁇ m to about 1 ⁇ m.
- the coarse particle fraction kaolin slurry is subjected to a beneficiation step and/or a degritting step, prior to the attrition grinding process.
- the coarse particle fraction kaolin slurry is subjected to both beneficiation and degritting processes.
- the invention can advantageously reduce the population of kaolin crystals that exist as stacks.
- the kaolin product of the invention can have superior coverage relative to standard kaolin in lightweight and ultra lightweight coated paper applications, as the higher population of individual plate crystals present in hyperplaty kaolin provides a relatively thin and uniform plate thickness.
- the invention provides a paper coated with hyperplaty kaolin, as described herein.
- Another aspect of the present invention provides an extender for paints, the extender comprising a coarse particle size kaolin having a d 50 ranging from about 0.25 ⁇ m to about 2.0 ⁇ m.
- the kaolin extender has a shape factor of greater than about 90.
- the extender can be prepared by attrition grinding a coarse particle size kaolin fraction, as described above.
- the extender is coarse, with a d 50 ranging from 0.25 ⁇ m to 2.0 ⁇ m, such as a d 50 ranging from 0.5 ⁇ m to 1.5 ⁇ m.
- the d 50 can be approximately 1.3 ⁇ m.
- control of sheen may not be required, and therefore the kaolin can comprise finer particles with a d 50 ranging from 0.25 ⁇ m to 1 ⁇ m.
- the d 50 can be approximately 0.6 ⁇ m.
- Another embodiment provides a paint comprising an extender comprising a coarse particle size kaolin having a d 50 ranging from 0.25 ⁇ m to 2.0 ⁇ m.
- the kaolin extender has a shape factor of at least 70:1, or any other value described herein.
- the kaolin extender has a shape factor of at least 100:1.
- Another aspect of the present invention provides an extender for paint comprising a kaolin, prepared by a method comprising providing a kaolin slurry comprising whole crude kaolin or a blend of whole crude and coarse-particle size fractions from a centrifuge, attrition grinding the kaolin slurry, removing the coarse particle size fraction from the slurry by centrifugation, and attrition grinding the coarse-particle size fraction to provide a kaolin product having a shape factor of at least about 70:1, or any of the shape factors described herein.
- Another aspect of the present invention relates to the use of the hyperplaty clay for filling, for example, paper or paperboard product, such as a supercalendered magazine paper filler product.
- the paper or paperboard product is filled with a kaolin having a shape factor value of at least about 70.
- Another aspect of the invention provides a method of making a matte paper coating, comprising: (a) attrition grinding a crude kaolin slurry comprising a blend of coarse-fractions from a centrifuge that have been degritted to 80% finer than 5 ⁇ m; (b) removing the coarse particle size fraction from the slurry by centrifugation; and (c) attrition grinding the coarse particle size fraction to provide kaolin having a shape factor of at least 70:1.
- Another aspect of the invention provides a method for producing a pigment product comprising:
- step (b) attrition grinding the suspension produced by step (a) by using a particulate grinding medium by a process in which the average shape factor of the kaolin clay is increased by at least 10, preferably at least 20;
- step (d) dewatering the suspension of ground kaolin clay separated in step (c) to recover a kaolin pigment therefrom.
- the kaolin clay may form from 20% to 70%, usually from 20% to 45% of the treated suspension.
- the kaolin clay can comprise a sedimentary kaolin clay, such as a sedimentary kaolin clay from Georgia, USA.
- the raw kaolin clay may have a psd such that not more than about 40% by weight comprises particles having an esd larger than 10 ⁇ m and not more than 50% by weight, e.g. from about 20% to about 40% by weight, comprising particles having an esd smaller than 2 ⁇ m.
- the shape factor of the kaolin clay treated in step (a) may be less than 15, such as in the range of from about 5 to about 10.
- the shape factor may be increased by a differential of at least 30, in some cases at least 40, e.g. from a shape factor value of less than 15 to a shape factor value greater than 55.
- a dispersing agent for the kaolin clay may or may not be added to the kaolin clay.
- the kaolin clay employed in step (a) may be a coarse component obtained from classifying, e.g. using a centrifuge, a standard blocky sedimentary kaolin clay, such as a kaolin clay having a shape factor of from 5 to 10.
- the coarse component may have not more than 50% by weight of particles having an esd less than 2 ⁇ m and not more than 10% by weight having an esd less than 0.25 ⁇ m.
- the psd of the kaolin clay may be adjusted by blending from 99 to 50 parts by weight of the kaolin clay with from 1 to 50 parts by weight, such as from 10 to 30 parts by weight, of a fine platy kaolin component, e.g. having a shape factor of at least 15, such as from 15 to 40 and whose percentages by weight of particles smaller than 2 ⁇ m and 0.25 ⁇ m are respectively at least 85% by weight and at least 20% by weight.
- the fine platy kaolin component may be a kaolin derived from either a primary or a sedimentary deposit.
- the fine platy kaolin component may be added to the kaolin or obtained from the coarse component prior to or after the grinding step (b). The addition may be carried out with the kaolins to be blended in either powdered, dry form or in the form of an aqueous suspension.
- a resulting kaolin product prepared by blending in the manner described can improve characteristics of the kaolin, such as the rheology and dewatering characteristics of a resulting aqueous suspension, and can provide better runnability and particle alignment when the kaolin is used in a coating composition.
- the kaolin clay may be subjected to one or more well known purification steps to remove undesirable impurities, e.g. between steps (a) and (b) or between steps (c) and (d).
- the aqueous suspension of kaolin clay may be subjected to a froth flotation treatment operation to remove titanium containing impurities in the froth.
- the suspension may be passed through a high intensity magnetic separator to remove iron containing impurities.
- Step (b) may comprise a process wherein the suspension of kaolin clay is treated by medium attrition grinding wherein an energy of from about 40 kWh to about 250 kWh per tonne of clay (on a dry weight basis) is dissipated in the suspension.
- the process of step (b) may comprise a process comprising at least two stages, namely a first stage (b1) wherein delamination of the kaolin clay occurs and a second stage (b2) wherein comminution of the platelets of the kaolin clay occurs.
- a gentle comminution step (b1) can be performed, such as grinding via a particulate grinding medium in order to break down composite particles, which are present in the raw kaolin clay.
- Such composite particles generally comprise coherent stacks or blocks of individual hexagonal plate-like particles, especially where the kaolin clay is from a sedimentary deposit.
- steps (b1) When the kaolin clay is subjected to relatively gentle comminution, e.g. by grinding in step (b1), many of the composite particles can be broken down to give the individual thin, substantially hexagonal plates, i.e., delamination, the result being an increase of the average shape factor of the kaolin clay.
- this process may increase the shape factor of the kaolin clay from a starting shape factor of about 5 to 10 to an increased shape factor of at least about 50 to 55.
- “relatively gentle grinding” we mean grinding in an attrition grinding mill with a particulate grinding medium, the contents of the attrition grinding mill being agitated by means of an impeller which rotates at a speed which is insufficient to set up a vortex in the suspension, such as at a peripheral speed below about 10 m.s ⁇ 1 and in which the amount of energy dissipated in the suspension during grinding is less than about 75 kWh, such as less than about 55 kWh per ton of kaolin clay on a dry weight basis.
- the particulate grinding medium can be of relatively high specific gravity, for example 2 or more, and may for example may comprise grains of silica sand, the grains generally having diameters not larger than about 2 mm and not smaller than about 0.25 mm.
- the second stage (b2) of the two stage form of step (b) can comprise grinding in an attrition grinding mill which is equipped with a stirrer capable of being rotated at a speed such that a vortex is formed in the suspension in the mill during grinding.
- the particulate grinding medium can have a specific gravity of 2 or more, and can comprise, for example, grains of silica sand where the grains can have diameters not larger than about 2 mm and not smaller than about 0.25 mm. If stage (b2) is preceded by a relatively gentle comminution in stage (b1), the amount of energy dissipated in the suspension of kaolin clay in stage (b2) can be in the range of from about 40 kWh to about 120 kWh per dry ton of kaolin clay.
- the amount of energy dissipated in the suspension of kaolin clay in step (b) can be in the range of from about 100 kWh to about 250 kWh per dry ton of kaolin clay.
- step (c) the suspension of ground kaolin clay can be separated from the particulate grinding medium in any manner known in the art, such by passing the suspension through a sieve of appropriate aperture size, for example a sieve having nominal aperture sizes in the range of from about 0.1 mm to about 0.25 mm.
- the kaolin clay may be further treated to improve one or more of its properties.
- high energy liquid working such as by using a high speed mixer, may be applied to the product in slurry form, e.g. before step (d) or after step (d) and subsequent re-dispersion in an aqueous medium, e.g. during makedown of a coating composition.
- the suspension of ground kaolin may be dewatered in one of the ways well known in the art, e.g. filtration, centrifugation, evaporation and the like.
- dewatering can be performed via a filter press.
- a filter press may be made to form a cake having a water content in the range of from about 15% to about 35% by weight.
- This cake may be mixed with a dispersing agent for the kaolin clay and can be converted into a fluid slurry, which may be transported and sold in this form.
- the kaolin clay may be thermally dried, for example by introducing the fluid slurry of the kaolin clay into a spray drier and transported in a substantially dry form.
- a fine platy kaolin component may be blended with the product of step (d) in the manner described earlier if such a component has not already been added prior to step (d).
- the pigment product may have a specific surface area as measured by the BET, N 2 method of at least 12 m 2 .g ⁇ 1 , preferably from 15 m 2 .g ⁇ 1 to 20 m 2 .g ⁇ 1 .
- pigment product produced in this aspect of the invention may be used in paper coating.
- the coating composition can be used for producing gloss coatings on paper and other substrates which composition comprises an aqueous suspension of a particulate pigment together with a hydrophilic adhesive or binder.
- the solids content of the paper coating composition may be greater than 60% by weight, such as a solids content of at least 70%, or even as high as possible but still giving a suitably fluid composition which may be used in coating.
- the composition may include a dispersing agent, e.g. up to 2% by weight of a polyelectrolyte based on the dry weight of pigment present, or any other dispersing agent known in the art, such as those described herein.
- the pigment product according to the first aspect of the invention may be used as the sole pigment in a paper coating composition, or it may be used in conjunction with one or more other known pigments, such as for example, (commercially available) kaolin, calcined kaolin, natural or precipitated calcium carbonate, titanium dioxide, calcium sulphate, satin white, talc and so called ‘plastic pigment’.
- the pigment product according to this aspect of the invention is present in the mixture in an amount of at least 80% of the total dry weight of the mixed pigments.
- the binder of the composition may comprise an adhesive derived from natural starch obtained from a known plant source as described herein, although it is not essential to use starch as a binder ingredient.
- Other binders, which may be used with or without starch are also described herein.
- the starch may be unmodified or raw starch, or it may be modified by one or more chemical treatments known in the art.
- the starch may, for example, be oxidized to convert some of its —CH 2 OH groups to —COOH groups. In some cases the starch may have a small proportion of acetyl, —COCH 3 , groups.
- the starch may be chemically treated to render it cationic or amphoteric, i.e., with both cationic and anionic charges.
- the starch may also be converted to a starch ether, or hydroxyalkylated starch by replacing some —OH groups with, for example, —OCH 2 CH 2 OH groups, —OCH 2 CH 3 groups or —OCH 2 CH 2 CH 2 OH groups.
- a further class of chemically treated starches that may be used is that known as the starch phosphates.
- the raw starch may be hydrolyzed by means of a dilute acid or an enzyme to produce a gum of the dextrin type.
- the starch binder used in the composition according to this aspect of the invention can be present in an amount ranging from 4% to 25% by weight, based on the dry weight of pigment.
- the starch binder may be used in conjunction with one or more other binders, for example synthetic binders of the latex or polyvinyl acetate or polyvinyl alcohol type.
- the amount of the starch binder can be present in an amount ranging from 2% to 20% by weight
- the amount of the synthetic binder can be present in an amount ranging from 2% to 12% by weight, both based on the weight of dry pigment.
- at least 50% by weight of the binder mixture comprises modified or unmodified starch.
- Another aspect of the present invention provides a method of forming a coated paper, comprising applying the kaolin composition to coat a sheet of paper and calendering the paper to form a gloss coating thereon.
- the gloss coating is formed on both sides of the paper.
- Another aspect of the present invention provides a method of making a coated paper comprising, coating a fibrous substrate with a paper coating composition comprising a filler comprising kaolin having a shape factor of at least about 70:1, or any of the shape factors described herein.
- Another aspect of the present invention provides a coated paper comprising a fibrous substrate and a coating on the substrate comprising kaolin having a shape factor of at least about 70:1, or any of the shape factors described herein.
- Another aspect of the present invention provides a method of making a filled paper comprising providing a fibrous substrate and adding to the substrate kaolin having a shape factor of at least about 70:1, or any of the shape factors described herein.
- Calendering is a well known process in which paper smoothness and gloss is improved and bulk is reduced by passing a coated paper sheet between calender nips or rollers one or more times.
- elastomer coated rolls are employed to give pressing of high solids compositions.
- An elevated temperature may be applied. Five or more passes through the nips may be applied.
- the paper after coating and calendering in the method according to this aspect may have a total weight per unit area ranging from 30 g.m ⁇ 2 to 70 g.m ⁇ 2 , such as from 49 g.m ⁇ 2 to 65 g.m ⁇ 2 , or further from 35 g.m ⁇ 2 to 48 g.m ⁇ 2 .
- the final coating can have a weight per unit area ranging from 3 g.m ⁇ 2 to 20 g.m ⁇ 2 , such as from 5 g.m ⁇ 2 to 13 g.m ⁇ 2 .
- Such a coating may be applied to both sides of the paper.
- the coated paper may be LWC or ULWC paper.
- the paper gloss may be greater than 45 TAPPI units and the Parker Print Surf value at a pressure of 1 MPa of each paper coating may be less than 1 ⁇ m.
- the gloss of a coated paper surface may be measured by means of a test laid down in TAPPI Standard No 480 ts-65. The intensity of light reflected at an angle from the surface of the paper is measured and compared with a standard of known gloss value. The beams of incident and reflected light are both at an angle of 75° to the normal to the paper surface. The results are expressed in TAPPI gloss units. In one embodiment, the gloss of the pigment product may be greater than 50, in some cases greater than 55, TAPPI units.
- the Parker Print Surf test provides a measure of the smoothness of a paper surface, and comprises measuring the rate at which air under pressure leaks from a sample of the coated paper which is clamped, under a known standard force, between an upper plate which incorporates an outlet for the compressed air and a lower plate, the upper surface of which is covered with a sheet of either a soft or a hard reference supporting material according to the nature of the paper under test. From the rate of escape of the air, a root mean cube gap in ⁇ m between the paper surface and the reference material is calculated. A smaller value of this gap represents a higher degree of smoothness of the surface of the paper under test.
- the binder present in the coating composition comprises starch.
- other known starch-free binders are employed (with or without starch present).
- the adhesive or binder may form from 4% to 30%, e.g., 8% to 20%, for example from 8% to 15% by weight of the solids content of the composition. The amount employed will depend upon the composition and the type of adhesive, which may itself incorporate one or more ingredients.
- the particulate kaolin according to the present invention may be mixed with other pigments, fillers and extenders to obtain a blend of properties provided by the constituents of the mixture.
- the added pigment, filler or extender material may comprise one or more of hydrous kaolin, calcined kaolin, aggregated kaolin, calcium carbonate (ground or precipitated) talc, gypsum or other known white particulate mineral or pigment material.
- Paper coatings and paper fillers according to the present invention include, in addition to the kaolin as described above, materials generally used in the production of paper coatings and paper fillers. Specifically, the compositions will include a binder and a pigment, typically TiO 2 .
- the fillers and coatings according to the present invention may optionally include other additives, including, but not limited to, dispersants, cross linkers, water retention aids, viscosity modifiers or thickeners, lubricity or calendering aids, antifoamers/defoamers, gloss-ink hold-out additives, dry or wet rub improvement or abrasion resistance additives, dry or wet pick improvement additives, optical brightening agents or fluorescent whitening agents, dyes, biocides, leveling or evening aids, grease or oil resistance additives, water resistance additives and/or insolubilisers.
- additives including, but not limited to, dispersants, cross linkers, water retention aids, viscosity modifiers or thickeners, lubricity or calendering aids, antifoamers/defoamers, gloss-ink hold-out additives, dry or wet rub improvement or abrasion resistance additives, dry or wet pick improvement additives, optical brightening agents or fluorescent whitening
- binders include, but are not limited to, adhesives derived from natural starch obtained from a known plant source, for example, wheat, maize, potato or tapioca; synthetic binders, including styrene butadiene, acrylic latex, vinyl acetate latex, or styrene acrylic; casein; polyvinyl alcohol; polyvinyl acetate; or mixtures thereof.
- Paper coatings have very different binder levels depending upon the type of printing to be used with the coated paper product. Appropriate binder levels based upon the desired end product would be readily apparent to the skilled artisan. Binder levels are controlled to allow the surfaces to receive ink without disruption.
- the latex binder levels for paper coatings generally range from about 3% to about 30%. In one embodiment according to the present invention, the binder is present in the paper coating in an amount of from about 3% to about 10%. In another embodiment according to the present invention, the binder is present in the coating in an amount ranging from about 10% to about 30% by weight.
- Another aspect of the present invention provides a method of making a barrier coating from a coarse fraction kaolin having the properties described herein. Barrier coatings are useful to impart to paper resistance to moisture, moisture vapor, grease, oil, air, etc.
- the amount of binder in the formulation may be very high on the order of 40% to 50%.
- the binder combined with the flattest possible plates result in a coating, which exhibits excellent barrier properties.
- Another aspect of the present invention provides a barrier coating composition, comprising a slurry comprising kaolin having a shape factor of at least about 70:1, or any of the shape factors described herein.
- the solids content of the slurry can range from about 45% to about 70%.
- Another aspect of the present invention provides a method of improving barrier properties in a paper comprising coating a fibrous substrate with a paper coating composition comprising a kaolin having a shape factor of at least about 70:1, or any of the shape factors described herein.
- Another aspect of the present invention provides a filler comprising a kaolin having a shape factor of at least about 70:1, or any of the shape factors described herein.
- Another aspect of the present invention provides a slurry comprising a kaolin having a shape factor of greater than 70:1 and a stabilizing agent.
- the kaolin can have a shape factor of at least about 80:1, or any of the shape factors described herein.
- the stabilizing agent comprises carboxymethylcellulose.
- the stabilizing agent can comprise a smectite clay.
- the stabilizing agent can comprise bentonite.
- the stabilizing agent can comprise hectorite.
- the stabilizing agent is present in the slurry in an amount ranging from about 4 pounds per dry tonne kaolin to about 10 lbs per dry tonne kaolin.
- the slurry has a solids content of greater than about 45%, such as a solids content ranging from about 50% to about 60%.
- Dispersants may be chosen from any art recognized dispersants for use in paper coating or paper filling compositions. Appropriate dispersants will be readily apparent to the skilled artisan. Dispersant may be chosen from polyelectrolytes such as polyacrylates and copolymers containing polyacrylate species, especially polyacrylate salts (such as sodium and aluminum optionally with a group II metal salt), sodium hexametaphosphates, non-ionic polyol, polyphosphoric acid, condensed sodium phosphate, non-ionic surfactants, alkanolamine and other reagents commonly used for this function.
- polyacrylates and copolymers containing polyacrylate species especially polyacrylate salts (such as sodium and aluminum optionally with a group II metal salt), sodium hexametaphosphates, non-ionic polyol, polyphosphoric acid, condensed sodium phosphate, non-ionic surfactants, alkanolamine and other reagents commonly used for this function.
- polyacrylate salts such
- the kaolin according to the present invention may be used as the sole pigment in the paper coatings and paper fillers of the present invention.
- the hyperplaty kaolin described above may be combined with another pigment.
- Additional pigments for use in the composition according to the present invention can be selected from any art recognized pigment. Pigments may be selected from other kaolin, calcined kaolin, natural or precipitated calcium carbonate, titanium dioxide, calcium sulphate, satin white, talc or other plastic pigments.
- a pigment can be TiO 2 .
- TiO 2 is present in an amount ranging from 0 to 30 parts, such as from 5-20 parts or from 10-20 parts.
- cross linkers are used in the coating or filling composition for use with the present invention, crosslinkers are generally present in levels of up to 5% by weight. Any art recognized crosslinker may be used. Appropriate crosslinkers include, but are not limited to, glyoxals, melamine formaldehyde resins, ammonium zirconium carbonates and mixtures thereof.
- water retention aids are generally present up to 2% by weight. Any art recognized water retention aid may be used. Appropriate water retention aids include, but are not limited to, sodium carboxymethyl cellulose, hydroxyethyl cellulose, PVA (polyvinyl acetate), starches, proteins, polyacrylates, gums, alginates, polyacrylamide bentonite and other commercially available products sold for such applications.
- a viscosity modifier or thickener is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized thickener or viscosity modifier may be used. Appropriate viscosity modifiers or thickeners include, but are not limited to, polyacrylates, emulsion copolymers, dicyanamide, triols, polyoxyethylene ether, urea, sulphated castor oil, polyvinyl pyrrolidone, montmorillonite, CMC (carboxymethyl celluloses), sodium alginate, xanthan gum, sodium silicate, acrylic acid copolymers, HMC (hydroxymethyl celluloses), HEC (hydroxyethyl celluloses) and mixtures thereof.
- a lubricity/calender aid is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized lubricity or calendering aid may be used. Appropriate lubricity or calendering aids include, but are not limited to, calcium stearate, ammonium stearate, zinc stearate, wax emulsions, waxes, alkyl ketene dimer, glycols and mixtures thereof.
- an antifoamer or defoamer is used in the coating or filling composition of the present invention, it is generally present in levels up to 1% by weight. Any art recognized antifoamer or defoamer may be used. Appropriate antifoamer and defoamers include, but are not limited to, blends of surfactants, tributyl phosphate, fatty polyoxyethylene esters plus fatty alcohols, fatty acid soaps, silicone emulsions and other silicone containing compositions, waxes and inorganic particulates in mineral oil, blends of emulsified hydrocarbons and other compounds sold commercially to carry out this function.
- dry or wet pick improvement additives are used in the coating or filling composition of the present invention, they are generally present in levels up to 2% by weight. Any art recognized dry or wet pick improvement additives may be used. Appropriate dry or wet pick improvement additives include, but are not limited to, melamine resin, polyethylene emulsions, urea formaldehyde, melamine formaldehyde, polyamide, calcium stearate, styrene maleic anhydride and mixtures thereof.
- dry or wet rub improvement and abrasion resistance additives are used in the coating or filling composition of the present invention, they are generally present in levels up to 2% by weight. Any art recognized dry or wet rub improvement and abrasion resistance additives may be used. Appropriate dry or wet rub improvement and abrasion resistance additives include, but are not limited to, glyoxal based resins, oxidized polyethylenes, melamine resins, urea formaldehyde, melamine formaldehyde, polyethylene wax, calcium stearate and mixtures thereof.
- a gloss-ink hold-out additive is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized gloss-ink hold out additive may be used. Appropriate gloss-ink hold out additives include, but are not limited to, oxidized polyethylenes, polyethylene emulsions, waxes, casein, guar gum, CMC, HMC, calcium stearate, ammonium stearate, sodium alginate and mixtures thereof.
- optical brightening agents (OBA) and fluorescent whitening agents (FWA) are used in the coating or filling composition of the present invention, they are generally present in levels up to 1% by weight. Any art recognized optical brightening agents (OBA) and fluorescent whitening agents (FWA) may be used. Appropriate optical brightening agents (OBA) and fluorescent whitening agents (FWA) include, but are not limited to, stilbene derivatives.
- a dye is used in the coating or filling composition of the present invention, it is generally present in levels up to 0.5% by weight. Any art recognized dye may be used.
- biocide/spoilage control agent is used in the coating or filling composition of the present invention, it is generally present in levels up to 1% by weight. Any art recognized biocide/spoilage agent may be used. Appropriate biocides/spoilage agents include, but are not limited to, metaborate, sodium dodecylbenene sulphonate, thiocyanate, organosulphur, sodium benzonate and other compounds sold commercially for this function such as the range of biocide polymers sold by Calgon Corporation.
- a leveling aid is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized leveling aid may be used. Appropriate leveling aids include, but are not limited to, non-ionic polyol, polyethylene emulsions, fatty acid, esters and alcohol derivatives, calcium stearate and other compounds sold commercially for this function.
- a grease and oil resistance additive is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized grease and oil resistance additive may be used. Appropriate grease and oil resistance additives include, but are not limited to, oxidized polyethylenes, latex, SMA (styrene maleic anhydride), polyamide, waxes, alginate, protein, CMC, HMC and mixtures thereof.
- a water resistance additive is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized water resistance additive may be used. Appropriate water resistance additives include, but are not limited to, oxidized polyethylenes, ketone resin anionic latex, polyurethane, SMA, glyoxal, melamine resin, urea formaldehyde, melamine formaldehyde, polyamide, glyoxals, stearates and other materials commercially available for this function.
- an insolubilizer is used in the coating or filling composition of the present invention, it is generally present in levels up to 2% by weight. Any art recognized insolubilizer may be used.
- the substrate to be filled or coated may be selected from any art recognized fibrous substrate.
- Substrates for use in the present invention include both wood based and woodfree substrates.
- Exemplary substrates according to the present invention are paper.
- the present invention can be used in the production of all paper grades, from ultra lightweight coated paper to coated or filled board.
- Lightweight coated, or LWC, paper is generally coated to a weight of from about 5 g.m ⁇ 2 to about 13 g.m ⁇ 2 on each side, and the total weight per unit area of the coated paper is generally in the range of from about 49 g.m ⁇ 2 to about 65 g.m ⁇ 2 .
- LWC paper is generally used for printing magazines, catalogues and promotional material.
- the coated paper is required to meet certain standards of surface gloss and smoothness.
- the paper is generally required to have a gloss value of at least about 32, and up to about 60, TAPPI units, and a Parker Print Surf value in the range of from about 0.5 to about 1.6 ⁇ m.
- Ultra lightweight coated, or ULWC, paper is sometimes otherwise known as light lightweight coated, or LLWC, paper and is used for catalogues and for advertising and promotional material sent through the mail to reduce mailing costs.
- the coating weight is generally in the range of from about 2 g.m ⁇ 2 to about 7g.m ⁇ 2 on each side, and the total weight per unit area of the coated paper is generally in the range of from about 25 g.m ⁇ 2 to about 48 g.m ⁇ 2 .
- Sheets may be coated on the sheet forming machine, i.e., “on-machine” or they may be coated on a coating machine, i.e., “off-machine.” Any art recognized coating method may be used to produce the coated sheet according to the present invention.
- the coating is applied to the sheet material by an applicator, and a metering device assures that the proper level of coating composition is applied. When an excess of coating composition is applied by the applicator, the metering device is downstream of the applicator. Alternatively, the correct amount of coating composition may be applied to the applicator by the metering device, such as a film press. While coating the sheet, the sheet may be supported by backing rolls or may be subjected only to tension.
- Examples of known coaters which may be used with the present invention include, but are not limited to, air knife coaters, blade coaters, rod coaters, bar coaters, multi-head coaters, roll coaters, roll/blade coaters, case coaters, liquid application systems, reverse roll coaters, extrusion coaters, and curtain coaters.
- the present invention may be used in the production of coated paper for printing. Any art recognized method of printing may be used with the coated paper according to the present invention. Appropriate printing techniques will be readily apparent to the skilled artisan.
- Printing techniques for use according to the present invention include, but are not limited to, rotogravure, offset printing, or flexo printing.
- Rotogravure involves the use of an engraved or etched cylinder as an image carrier. Image areas are etched or engraved below non-image areas in the form of tiny sunken cells. The cylinder is immersed in ink, and the excess ink is scraped off by a blade. When the substrate contacts the printing cylinder, ink transfers, forming the image.
- Offset printing is an indirect printing method in which the inked image on a press plate is first transferred to a rubber blanket that, in turn, “offsets” the inked impression to a press sheet.
- This example illustrates a method of refining kaolin to produce a high shape factor kaolin, i.e., greater than or equal to 70, either as a dry kaolin or a kaolin slurry that is stabilized by adding additional water and carboxymethyl cellulose (a thickener).
- a “stabilized slurry” refers to a slurry where the kaolin does not appreciably settle out of solution over time. It would be expected that adding additional water would have provided a less stabilized slurry.
- a CMC carboxymethylcellulose
- FIG. 1 is a flowchart outlining the process of providing a high shape factor kaolin.
- a Georgia coarse crude kaolin is blunged, degritted, and subjected to magnetic separation. After a first attrition grinding step with sand, the product is classified to separate the coarse fraction from the fines. The coarse fraction is subjected to a second attrition grinding step, followed by leaching and filtering.
- a dry kaolin can be prepared by drying in a spray dryer, whereas a kaolin slurry can be prepared, such as a slurry further comprising CMC, biocide and a dispersant.
- FIG. 2 is a flowchart outlining a process for the preparation of a high shape factor kaolin.
- a Georgia crude kaolin is subjected to blunging and degritting steps, followed by magnetic separation and a first attrition grinding step.
- the product is then classified where the coarse fraction is subjected to a second attrition grinding step, followed by another classification to obtain a product where 70% of the particles have an esd less than 2 ⁇ m.
- This product is then leached and filtered, followed by the formation of either a dry kaolin product or a slurry.
- This Example provides another process where a Georgia crude kaolin is reblunged and degritted, as illustrated in the flowchart of FIG. 3. After selective flocculation, the kaolin is subjected to magnetic separation. A coarse fraction from a size classification centrifuge is then added to the kaolin prior to a first attrition grinding step. After a size classification, the coarse fraction is subjected to a second attrition grinding step, followed by leaching and filtering to produce a high shape factor product.
- FIG. 4 is a flowchart illustrating a process for making a barrier coating pigment from coarse fraction kaolin prepared according to the method of Example 1, where the barrier coating comprises kaolin having a shape factor of at least about 90:1.
- 5 gallons of coarse hyperplaty fraction kaolin is obtained in accordance with one of the previously described embodiments of the invention.
- the slurry is adjusted to have a solids content of 35%. 1 lb/ton C-211 is added, and more can be added if necessary.
- the batch is subjected to sand grinding to increase the percentage of particles having a size of less than 2 ⁇ m by 24% to 26%. 3600 mL sand and 1800 mL clay slip was used. In the final slurry, at least 55% of the solids had a size less than 2 ⁇ m.
- SAPA a blend of 35% Sodium Polyacrylate and 65% Soda Ash
- Kaolin samples A-C were tested for grease and oil barrier properties. Samples A and B are known kaolin products whereas sample C is a kaolin product prepared in accordance with the method of Example 1. Barrier coatings were prepared as described in this Example, with these kaolin products. Sample A - Sample B - Sample C - Comparative Comparative Invention PSD % 82.4 89.9 56.0 ⁇ 2 ⁇ m Panacea - 35 58.9 92 Shape Factor
- Barrier coatings were applied to a 60 g/m 2 woodfree base sheet with a cylindrical laboratory coater.
- the coatings comprised the kaolin, calcium carbonate, latex, calcium stearate, and a viscosity modifier.
- the physical properties of the kaolins can be found in the table, above.
- the barrier coatings were applied twice on the same paper sample.
- the coated paper samples were finished on a laboratory scale calender.
- the 3M test kit was developed to determine the effectiveness of fluorochemical treated papers.
- the tests involve exposing the paper to a series of solution, which contain castor oil, heptane and toluene. There are 12 solutions of levels in the Kit test. As the Kit levels increase the proportion of solvent is larger.
- the OGR test involves exposing the coated paper samples to a suitable oil or oil containing compound for a set period of time. The amount of oil that seeps through the coated sample and is absorbed on an underlying blotter is quantified. The test values from the OGR represent that percentage of the blotter paper covered by the oil. Thus, lower values are preferred. OGR values of 3 and less denote fully satisfactory products.
- the sample according to the present invention provides stronger barriers when compared with prior art kaolins. Such results can be attributed to the high shape factor and large plate diameter associated with the kaolins of the present invention.
- Example 5 illustrates the utility of the inventive kaolin compositions as a component of a paper coating.
- Paper coating formulations were made up based upon 100 parts of pigment with 14 parts Dow 692 latex binder, 4 parts PROCOTE protein binder, 1.1 parts DISPEX polyacrylate dispersant, TiO 2 and kaolin were added as indicated in the Table, below.
- kaolin properties are set forth in the Table below: Prior Art Kaolin Invention Kaolin 1 Invention Kaolin 2 Brightness 90 91 92 2 micron 91 85.6 66.7 0.5 micron 35 34.4 18.1 Shape Factor 15 107 141 Surface Area 15 15.9 11.3 Steepness 45 37 33
- Samples according to the present invention exhibited improved brightness at accepted TiO 2 levels and comparable brightness at lower TiO 2 levels. See FIG. 5 which plots the brightness results noted above as a function of TiO 2 content. Paper coated according to the present invention gives high brightness even with TiO 2 , significantly above the brightness of the uncoated sheet.
- inventive kaolin compositions are useful in applications wherein a high opacity, brightness or scattering are required, such as in brown board coating applications and may serve to reduce the amount of TiO 2 required therein.
- present example illustrates the utility of the inventive kaolin as a paper coating, the composition could also be used to coat other substances wherein a high brightness or opacity coating is needed.
- inventive kaolins as a filler, handsheets were prepared from a unbleached natural Kraft which has undergone no refining. While the present example pertains to use as a paper filler, it is anticipated that the inventive kaolins could also be useful as a high opacity filler for plastics and like materials.
- the handsheets were made with a TAPPI sheet mold at a pH of 4.5.
- the sheets were made on a fourdinier paper machine using unbleached hardwood kraft. The conditions are discussed in the table, below.
- pH 6.75 Freeness (CSF) 470 Freeness (CSF) after beating 380 Britt Fines % Fiber 80.3 % Fines 18.9 % Ash 0.8 Brightness 22.7 Specific Conductivity 1750 Mutek PCD: ⁇ 340 Total Dissolved Solids 2327 ppm Inorganic Dissolved 1880 ppm
- the handsheets were air dried and a range of properties were measured for unfilled sheets, sheets made using the commercially available prior art pigment ASTRAPLATE (available from Imerys, Inc.) and two sets of samples using the composition identified as Invention Kaolin 2 in Example 5 above.
- ASTRAPLATE and Invention 2 Samples included 2 lbs per ton of a commercially available retention aid of a sort that would be readily obtainable by one of ordinary skill in the art.
- Filled paper was made using a bleached hardwood, softwood mixture beaten to a 400 Canadian Standard Freeness (CSF), a retention aid, and Invention Kaolin 2 of Example 5. The pH was maintained at 5.0. Handsheet were made and allowed to air dry. A range of properties were measured.
- the pigment light scatter according to the present invention (1900-2000 cm 2 /g) compares favorably with that which can be achieved using calcined clay at 2500 and standard filler clay at 1100.
- the ground Invention Kaolin 3 had good color, better than the existing fine particle size clay product. Further improvements may be possible through bleaching of the ground clay.
- the light Carbolite grinding of Invention Kaolin 3 can provide a product comprising a coarse, high shape factor clay giving a combination of low sheen with significant opacity improvements. These results reflect the performance of a small batch of material.
- the more highly ground Invention Kaolin 3 can have a fine high shape factor clay giving large opacity improvements, at the cost of increased sheen.
- Such a product may offer an alternative to calcined clays in formulations where high scrub resistance is not regarded as important.
- FIG. 6 presents the opacity and sheen of the ground clays in the high PVC formulation.
- the clays were prepared by grinding with fine Carbolite media. The grinding energy is indicated by the size of each point. To allow comparison some standard clays (SUPREME and GLOMAX LL*, all of which are Imerys clay products) are plotted.
- Invention Kaolin 4 had a poor color, a substantial part of their opacity originated from absorption, rather than scattering of light. They also ground to a finer particle size than Invention Kaolin 3, resulting in higher sheen.
- a 1.5 unit increase in opacity was achievable by Carbolite grinding of the fine particle size clay feed material. Similar opacities were obtained with the ground Georgia Feed Clay. For these materials, any increase in opacity was always accompanied by a significant increase of the sheen, brought about by a decreasing particle size.
- FIG. 7 is a plot of the d 50 versus shape factor. For each of the four feeds, the Carbolite grinding resulted in an increase in the clay's shape factor, and a decrease in the mean particle size. From FIG. 7, it can be seen that Invention Kaolin 3 and Invention Kaolin 4 yielded the highest shape factors. Invention Kaolin 4 suffered from poor color, with an ISO brightness of 75.7.
- Invention Kaolin 3 had good color in that it is better than that of the existing fine particle size clay product.
- FIG. 8 is a flowchart outlining a process where two coarse fractions are combined, followed by leaching and filtering to produce a stabilized high-solids slurry by adding a stabilizing agent such as carboxymethlycellulose or a smecite clay (i.e. bentonite, hectorite, montmorillonite, etc.).
- a stabilizing agent such as carboxymethlycellulose or a smecite clay (i.e. bentonite, hectorite, montmorillonite, etc.).
- a two tote sized samples ( ⁇ 250-300 gallons) of the inventive product of Example 9 were made down by blunging with a 65/35 SAPA (soda ash/sodium polyacrylate) dispersant package to a pH of 6.5.
- the two sample totes of the product were each treated with biocide (1 lb/dry tonne Proxel) then treated with 8 lbs/dry tonne of the carboxymethylcellulose PE-30 EX.
- the final solids content of Sample 1 was 52% and the final solids content of sample 2 was 49.6%.
- the initial Hercules viscosity of samples 1 and 2 were measured using a no. 2 spindle at 20 rpm and found to be 30 cps and 18 cps respectively.
- the initial Hercules viscosity of sample 1 was measured as 8.5 dynes at 4400 rpm at pH 7.2 and the initial Hercules viscosity of sample 2 was measured as 5.0 dynes at pH 7.0.
- each one pint sample was subjected to a pour test wherein it was upended and allowed to pour for 1 minute. In this time approximately 93.4% sample 1 and 94.9% of sample 2 was seen to pour from the container, illustrating the continued fluidity of the sample.
- a similar test performed on each entire tote ( ⁇ 250-300 gallons) of samples 1 and 2 resulted in 99.7% and 99.2% pouring respectively.
- the CMC stabilized slurry is basically stable, which is surprising in light of the fact that the make down process with CMC results in an effective decrease in the slurry solids. Generally this process should be useful in relation to slurries having a solids content, for example, in the range of greater than about 45%, between about 45% and about 60%, or even in the range of about 50 to about 60%.
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US10/233,599 US20030085012A1 (en) | 2001-09-07 | 2002-09-04 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/086,563 US7226005B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/086,575 US7208039B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/108,878 US7214264B2 (en) | 2001-09-07 | 2005-04-19 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
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US31820701P | 2001-09-07 | 2001-09-07 | |
US10/233,599 US20030085012A1 (en) | 2001-09-07 | 2002-09-04 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
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US11/086,575 Division US7208039B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/086,563 Division US7226005B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/108,878 Continuation US7214264B2 (en) | 2001-09-07 | 2005-04-19 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
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US11/086,563 Expired - Lifetime US7226005B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/086,575 Expired - Lifetime US7208039B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/108,878 Expired - Lifetime US7214264B2 (en) | 2001-09-07 | 2005-04-19 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
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US11/086,575 Expired - Lifetime US7208039B2 (en) | 2001-09-07 | 2005-03-23 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US11/108,878 Expired - Lifetime US7214264B2 (en) | 2001-09-07 | 2005-04-19 | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
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EP (2) | EP1425351B1 (zh) |
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Citations (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2158987A (en) * | 1934-11-26 | 1939-05-16 | Georgia Kaolin Co | Clay product and process of preparing same |
US3034859A (en) * | 1959-04-27 | 1962-05-15 | Southern Clays Inc | Delaminated english clay products, etc. |
US3171718A (en) * | 1962-02-16 | 1965-03-02 | Freeport Sulphur Co | Delaminated domestic sedimentary clay products and method of preparation thereof |
US3526768A (en) * | 1964-03-06 | 1970-09-01 | Union Oil Co | 2-substituted naphth(1,2)oxazole scintillators |
US3615806A (en) * | 1968-12-10 | 1971-10-26 | Georgia Kaolin Co | Kaolin pigments and methods of producing the same |
US3635662A (en) * | 1969-12-05 | 1972-01-18 | Georgia Kaolin Co | Kaolin product and method of producing the same |
US3798044A (en) * | 1972-06-07 | 1974-03-19 | Huber Corp J M | Process for manufacturing calcined kaolinitic clay products |
US4125411A (en) * | 1958-09-30 | 1978-11-14 | Yara Engineering Corporation | Kaolin product |
US4176148A (en) * | 1971-08-30 | 1979-11-27 | Princeton Chemical Research, Inc. | Method of manufacturing microporous paper-like butene-1 polymer sheets |
US4183991A (en) * | 1977-05-02 | 1980-01-15 | Rohm And Haas Company | Process for preparing highly filled acrylic articles |
US4198333A (en) * | 1977-09-02 | 1980-04-15 | Bayer Aktiengesellschaft | Stable suspensions of inorganic fillers in organic polyhydroxyl compounds containing completely or partially neutralized carboxyl groups |
US4221697A (en) * | 1974-05-29 | 1980-09-09 | Imperial Chemical Industries Limited | Composite materials |
US4225496A (en) * | 1977-07-27 | 1980-09-30 | Borden, Inc. | Acrylic latex cove base cement |
US4227920A (en) * | 1978-07-18 | 1980-10-14 | Yara Engineering Corporation | Methods of clay benefication |
US4233199A (en) * | 1979-07-03 | 1980-11-11 | Visvaldis Abolins | Flame resistant thermoplastic compositions with well balanced physical properties |
US4234469A (en) * | 1976-07-29 | 1980-11-18 | Idemitsu Kosan Company Limited | Flame retarding polyolefin resin blend composition |
US4241142A (en) * | 1978-12-20 | 1980-12-23 | Engelhard Minerals & Chemicals Corporation | Clay pigment for coating paper |
US4243574A (en) * | 1979-03-30 | 1981-01-06 | E. I. Du Pont De Nemours And Company | Poly(meta-phenylene isophthalamide) molding compositions |
US4298711A (en) * | 1980-04-09 | 1981-11-03 | Cargill Incorporated | Low shrink unsaturated polyester resinous composition |
US4311635A (en) * | 1980-08-25 | 1982-01-19 | Pantasote Inc. | Flame resistant thermoplastic elastomer |
US4359497A (en) * | 1971-08-30 | 1982-11-16 | Princeton Chemical Research, Inc. | Paper-like butene-1 polymer compositions |
US4381948A (en) * | 1979-07-26 | 1983-05-03 | Anglo-American Clays Corporation | Anhydrous kaolin clay pigment and method of preparation |
US4409344A (en) * | 1980-04-09 | 1983-10-11 | Cargill Incorporated | Low shrink unsaturated polyester resinous composition |
US4414352A (en) * | 1979-05-01 | 1983-11-08 | General Electric Company | Thermoplastic molding compositions and process |
US4427450A (en) * | 1980-08-04 | 1984-01-24 | Engelhard Corporation | Chalking-resistant, calcined kaolin clay pigment and method of making |
US4467057A (en) * | 1978-12-06 | 1984-08-21 | General Electric Company | Modified polyester composition |
US4543287A (en) * | 1980-07-11 | 1985-09-24 | Imperial Chemical Industries Limited | Fibrous material comprised of vermiculte coated fibers |
US4546126A (en) * | 1983-07-13 | 1985-10-08 | Ciba Geigy Corporation | Flame-retarding, reinforced moulding material based on thermoplastic polyesters and the use thereof |
US4582866A (en) * | 1984-04-30 | 1986-04-15 | E. I. Du Pont De Nemours And Company | Flame retardant thermoplastic multi-block copolyester elastomers |
US4584333A (en) * | 1984-01-17 | 1986-04-22 | Les Cables De Lyon | Fire-resistant thermoplastic composition |
US4708975A (en) * | 1986-04-02 | 1987-11-24 | E. I. Du Pont De Nemours And Company | Low smoke generating, high char forming, flame retardant thermoplastic multi-block copolyesters |
US4795776A (en) * | 1987-01-29 | 1989-01-03 | Dixon International Limited | Fire-resistant composition |
US4820761A (en) * | 1983-07-19 | 1989-04-11 | Sumitomo Chemical Company, Limited | Aromatic polysulfone resin composition |
US4873116A (en) * | 1986-09-30 | 1989-10-10 | Union Carbide Chemicals And Plastics Company Inc. | Method of preparing mixtures of incompatible hydrocarbon polymers |
US4888315A (en) * | 1986-06-04 | 1989-12-19 | Georgia Kaolin Company, Inc. | High solids blended kaolin clay slurry |
US4889886A (en) * | 1986-12-10 | 1989-12-26 | Polyplastics Co., Ltd. | Liquid crystal polyester composition |
US4918127A (en) * | 1986-12-31 | 1990-04-17 | Bp Performance Polymers, Inc. | Filled elastomer blends |
US4943324A (en) * | 1988-05-23 | 1990-07-24 | Georgia Kaolin Company, Inc. | High performance paper filler and method of producing same |
US4966638A (en) * | 1989-06-13 | 1990-10-30 | Lestox, Inc. | Silicone mixture and method of using it |
US4981521A (en) * | 1988-05-09 | 1991-01-01 | W. R. Grace & Co.-Conn. | Sprayable fireproofing composition |
US5085707A (en) * | 1988-05-23 | 1992-02-04 | Georgia Kaolin Company, Inc. | Defined and delaminated kaolin product |
US5112782A (en) * | 1989-05-04 | 1992-05-12 | Engelhard Corporation | Cationically processed calcined kaolin clay |
US5128606A (en) * | 1990-01-22 | 1992-07-07 | Ecc International Limited | Aspect radio measurement |
US5168083A (en) * | 1990-05-09 | 1992-12-01 | Georgia Kaolin Company, Inc. | High opacity defined kaolin product and method of producing same |
US5167707A (en) * | 1991-03-29 | 1992-12-01 | J. M. Huber Corporation | High performance coarse particle size sams pigments for paint and plastics applications |
US5169443A (en) * | 1991-11-13 | 1992-12-08 | Engelhard Corporation | Paper coating kaolin pigments there preparation and use |
US5294654A (en) * | 1991-08-12 | 1994-03-15 | General Electric Company | Flame-retarded, conductive compositions which include polyphenylene ether and polystyrene resins |
US5332493A (en) * | 1992-04-28 | 1994-07-26 | Ecc International Inc. | Method for improving rheological properties of kaolin clays |
US5364899A (en) * | 1992-01-24 | 1994-11-15 | Denki Kagaku Koguo Kabushiki Kaisha | Flame-retardant resin composition |
US5416151A (en) * | 1990-09-14 | 1995-05-16 | Mitsui Petrochemical Industries, Ltd. | Polymer composition and its use |
US5439558A (en) * | 1992-04-25 | 1995-08-08 | Stora Feldmuhle Ag | Print substrate |
US5454865A (en) * | 1993-12-23 | 1995-10-03 | Ecc International Inc. | Method for preparing refined kaolin in clay products |
US5516829A (en) * | 1992-08-10 | 1996-05-14 | Davis; James A. | Heat seamable flame retardant roof sheeting with highly crystalline thermoplasticity promoters and method for covering roofs |
US5522924A (en) * | 1995-03-17 | 1996-06-04 | Ecc International Inc. | Method for producing high brightness low abrasion calcined kaolin pigment |
US5573946A (en) * | 1988-02-25 | 1996-11-12 | Pfizer Inc. | Biologically pure culture of Streptomyces hygroscopicus ATCC 53718 capable of producing antibiotic compounds |
US5578659A (en) * | 1994-07-04 | 1996-11-26 | Polyplastics Co., Ltd. | Polyarylene sulfide resin composition |
US5624488A (en) * | 1995-06-30 | 1997-04-29 | Engelhard Corporation | Ultrahigh brightness calcined clay pigment, manufacture & use thereof |
US5646635A (en) * | 1995-08-17 | 1997-07-08 | Centurion International, Inc. | PCMCIA antenna for wireless communications |
US5685900A (en) * | 1995-10-18 | 1997-11-11 | Ecc International Inc. | Method for beneficiating discolored kaolin to produce high brightness coating clay |
US5707912A (en) * | 1996-03-18 | 1998-01-13 | Thiele Kaolin Company | Process for the treatment of clay materials to provide slurries having improved rheological properties |
US5735946A (en) * | 1996-05-14 | 1998-04-07 | U.S. Borax, Inc. | Two-stage process for delaminating kaolin |
US5749958A (en) * | 1995-02-07 | 1998-05-12 | Engelhard Corporation | Delaminated kaolin pigments their preparation and use in paper coating |
US5810998A (en) * | 1997-06-05 | 1998-09-22 | Thiele Kaolin Company | Process for improving the brightness of fine-grained kaolin clays |
US5846309A (en) * | 1997-02-20 | 1998-12-08 | J. M. Huber Corporation | Coarse particle size kaolin clay and method |
US5879512A (en) * | 1995-10-13 | 1999-03-09 | Ecc Internatinal Ltd. | Paper coating |
US5925454A (en) * | 1995-07-11 | 1999-07-20 | W.R. Grace & Co.-Conn. | Film having modified surface characteristics through use of combination of spherical and lamellar particulates |
US5948156A (en) * | 1994-03-28 | 1999-09-07 | Sud-Chemie, Ag | Supplementary agent for mineral binder systems |
US6031036A (en) * | 1992-10-07 | 2000-02-29 | General Electric Company | Flame resistant thermoplastic blends having reduced drippage |
US6149723A (en) * | 1998-07-22 | 2000-11-21 | Imerys Pigments, Inc. | Engineered kaolin pigment composition for paper coating |
US6186335B1 (en) * | 1998-03-20 | 2001-02-13 | Thiele Kaolin Company | Process for beneficiating kaolin clays |
US6262161B1 (en) * | 1997-06-26 | 2001-07-17 | The Dow Chemical Company | Compositions having improved ignition resistance |
USRE37385E1 (en) * | 1985-09-30 | 2001-09-18 | Kabushiki Kaisha Toyoto Chuo Kenkyusho | Composite material and process for manufacturing same |
US6402286B1 (en) * | 2001-02-09 | 2002-06-11 | Industrial Technology Research Institute | Function test device for optical print head heaters in thermal bubble printers |
US6564199B1 (en) * | 1999-04-01 | 2003-05-13 | Imerys Pigments, Inc. | Kaolin clay pigments, their preparation and use |
US6758895B2 (en) * | 2000-08-17 | 2004-07-06 | Imerys Minerals Limited | Particulate mineral materials |
Family Cites Families (169)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US37385A (en) * | 1863-01-13 | Improvement in machines for manufacturing chenille | ||
GB240398A (en) | 1925-07-10 | 1925-10-01 | Napier & Son Ltd | Improvements in or relating to valve operating mechanism for internal combustion engines |
US2414391A (en) * | 1943-03-04 | 1947-01-14 | Us Rubber Co | Manufacture of articles of rubberlike material |
US2531396A (en) | 1947-03-29 | 1950-11-28 | Nat Lead Co | Elastomer reinforced with a modified clay |
US2883356A (en) * | 1953-05-27 | 1959-04-21 | Monsanto Chemicals | Composition containing a plastic material and a modified clay |
GB819050A (en) | 1957-03-19 | 1959-08-26 | Huber Corp J M | Process and compositions for producing stable clay-filled chlorine-containing resins |
FR1299089A (fr) | 1961-06-09 | 1962-07-20 | Cellophane Sa | Nouveau procédé de fabrication de pellicules très peu perméables au gaz et à la vapeur d'eau |
GB1034364A (en) | 1962-10-30 | 1966-06-29 | Scott Bader Co | Improvements in or relating to the manufacture of polyvinylidene chloride copolymer emulsions |
GB1032536A (en) | 1964-05-04 | 1966-06-08 | English Clays Lovering Pochin | Improvements in or relating to the coating of paper and the like |
GB1118723A (en) | 1964-12-18 | 1968-07-03 | Berk Ltd | Polyolefin-and polyamide-containing compositions |
FR1439909A (fr) | 1965-02-18 | 1966-05-27 | Exxon Standard Sa | émulsions pâteuses de liants hydrocarbonés résistant aux hydrocarbures |
GB1101950A (en) | 1965-10-19 | 1968-02-07 | Grace W R & Co | Improvements in the production of polyethylene film |
GB1136350A (en) | 1966-11-25 | 1968-12-11 | Grace W R & Co | Improvements relating to non-permeable polymer films |
DE1760653A1 (de) | 1967-06-20 | 1972-03-16 | Combinet Paper Mills Inc | Wandbekleidung,insbesondere Tapete,und Verfahren zu ihrer Herstellung |
US3463350A (en) * | 1967-10-19 | 1969-08-26 | Continental Can Co | Plastic container for foodstuffs susceptible to oxidative deterioration |
DE1908699B2 (de) | 1969-02-21 | 1975-06-26 | Wolff Walsrode Ag, 3030 Walsrode | Verwendung eines wäßrig dispergieren Beschichtungsmittel zur Erzeugung von Überzügen auf Flächengebilden aus Kunststoff und/oder Metall |
US3663260A (en) * | 1970-07-20 | 1972-05-16 | Standard Oil Co | Talc filled metallizable polyolefins |
US3790402A (en) * | 1970-09-04 | 1974-02-05 | Grace W R & Co | Saran-aluminum silicate coating |
NL7209141A (zh) | 1971-08-30 | 1973-03-02 | ||
JPS515383Y2 (zh) | 1972-03-01 | 1976-02-14 | ||
US4082880A (en) * | 1973-11-22 | 1978-04-04 | Du Pont Of Canada Limited | Paper-like thermoplastic film |
JPS5316063Y2 (zh) | 1974-03-27 | 1978-04-27 | ||
JPS5637255B2 (zh) | 1974-05-28 | 1981-08-29 | ||
GB1493393A (en) | 1974-05-29 | 1977-11-30 | Ici Ltd | Fluid curable compositions containing particulate fillers and composite polymeric materials obtained therefrom |
GB1469028A (en) | 1974-09-17 | 1977-03-30 | English Clays Lovering Pochin | Comminution of solids |
JPS5410394Y2 (zh) | 1975-06-06 | 1979-05-14 | ||
DD127023B1 (de) | 1976-07-28 | 1982-03-31 | Karl Hoeffl | Mahlanlage zur feinzerkleinerung von mineralien |
US4102974A (en) * | 1977-04-26 | 1978-07-25 | The Continental Group, Inc. | Polyolefin containers having improved gas barrier properties |
JPS5621609Y2 (zh) | 1977-09-09 | 1981-05-21 | ||
WO1980001167A1 (en) | 1978-12-06 | 1980-06-12 | Gen Electric | Modified polyester compositions |
US4251765A (en) * | 1979-02-07 | 1981-02-17 | The United States Of America As Represented By The Secretary Of The Air Force | Aircraft electrical system tester |
JPS55129439U (zh) | 1979-03-06 | 1980-09-12 | ||
JPS5718652Y2 (zh) | 1979-03-12 | 1982-04-19 | ||
WO1980002430A1 (en) | 1979-05-01 | 1980-11-13 | Gen Electric | Thermoplastic molding composition and process |
GB2058734B (en) | 1979-09-19 | 1983-07-20 | English Clays Lovering Pochin | Paper coating pigments |
DE3024205C2 (de) * | 1980-06-27 | 1990-11-15 | Felix Schoeller jr. GmbH & Co KG, 4500 Osnabrück | Aufzeichnungspapier für Tintenspritzaufzeichnungsverfahren |
DE3047269C2 (de) | 1980-12-16 | 1983-08-04 | AEG-Telefunken Kabelwerke AG, Rheydt, 4050 Mönchengladbach | "Thermoplastische Polymermischung" |
US4528235A (en) * | 1982-08-05 | 1985-07-09 | Allied Corporation | Polymer films containing platelet particles |
US4728478A (en) * | 1982-08-05 | 1988-03-01 | Allied-Signal Inc. | Polymer films containing platelet particles |
PT77224B (en) | 1983-08-19 | 1987-03-26 | Dow Chemical Co | Process for preparing olefin polymer barrier films and methods of use thereof |
US4738726A (en) | 1985-05-06 | 1988-04-19 | Engelhard Corporation | Treatment of clays with cationic polymers to prepare high bulking pigments |
JPH0615227B2 (ja) | 1985-06-05 | 1994-03-02 | 出光石油化学株式会社 | 樹脂積層体 |
GB8521646D0 (en) * | 1985-08-30 | 1985-10-02 | English Clays Lovering Pochin | Inorganic fillers |
ZA867242B (en) | 1985-09-27 | 1987-05-27 | Dsg Schrumpfschlauch Gmbh | Heat shring tubing |
DE3632606A1 (de) | 1985-09-27 | 1987-04-02 | Dsg Schrumpfschlauch Gmbh | Zusammensetzung von waermeschrumpfendem polymeren kunststoff zur herstellung waermeschrumpfender erzeugnisse sowie daraus hergestellter artikel |
DE3536371C1 (de) | 1985-10-11 | 1987-05-07 | Metzeler Schaum Gmbh | Schwer entflammbarer Polyurethan-Schaumstoff |
DE3540524A1 (de) | 1985-11-15 | 1987-05-27 | Bayer Ag | Fuellstoffhaltige intumeszenzmassen auf epoxidharzbasis |
IE873315L (en) | 1986-12-31 | 1988-06-30 | Flork Michel | Filled elastomer blends |
KR910008819B1 (ko) | 1988-07-25 | 1991-10-21 | 스미도모덴기고오교오 가부시기가이샤 | 난연성수지 조성물 및 난연성절연전선 |
EP0361203B1 (en) * | 1988-09-13 | 1994-04-27 | Nippon Oil And Fats Company, Limited | Synthetic resin compositions |
WO1990011605A1 (en) | 1989-03-29 | 1990-10-04 | Lestox, Inc. | Electric cable with improved burn resistance feature |
DE3935682A1 (de) * | 1989-10-26 | 1991-05-02 | Messerschmitt Boelkow Blohm | Elektrischer antriebsmotor, insbesondere fuer steuer- und regelzwecke |
US5109051A (en) * | 1990-03-13 | 1992-04-28 | The B. F. Goodrich Company | Aluminosilicate compositions as partial replacement for titanium dioxide in pigmented polyvinyl chloride and polyvinyl chloride type compositions |
US5153039A (en) | 1990-03-20 | 1992-10-06 | Paxon Polymer Company, L.P. | High density polyethylene article with oxygen barrier properties |
SE467772B (sv) * | 1991-01-09 | 1992-09-14 | Tetra Alfa Holdings | Foerpackningsmaterial jaemte anvaendning av materialet foer framstaellning av behaallare |
SE468635B (sv) | 1991-01-09 | 1993-02-22 | Tetra Alfa Holdings | Foerpackningsmaterial jaemte anvaendning av materialet foer framstaellning av behaallare med goda syrgastaethetsegenskaper |
US5656635A (en) * | 1993-06-08 | 1997-08-12 | Allergan | 5-trans-alcohols and their use as ocular hypotensives |
JPH04270650A (ja) | 1991-02-26 | 1992-09-28 | Toyobo Co Ltd | ガスバリアー性フイルム |
CA2061644A1 (en) | 1991-03-05 | 1992-09-06 | Hisao Tanaka | Thermoplastic resin composition |
JP3213630B2 (ja) * | 1991-07-25 | 2001-10-02 | 三菱製紙株式会社 | インクジェット記録シート |
CA2083068C (en) | 1991-11-18 | 2002-08-20 | Pentti Rissanen | Wallpaper |
US5981011A (en) * | 1992-01-22 | 1999-11-09 | A*Ware Technologies, L.C. | Coated sheet material |
CA2089613A1 (en) | 1992-03-12 | 1993-09-13 | John H. Hung | Dispersion and method for producing same |
US5700560A (en) | 1992-07-29 | 1997-12-23 | Sumitomo Chemical Company, Limited | Gas barrier resin composition and its film and process for producing the same |
JPH06116382A (ja) | 1992-08-21 | 1994-04-26 | Hodogaya Chem Co Ltd | 軟質ポリカーボネート樹脂 |
DE4230742C2 (de) | 1992-09-14 | 1994-11-24 | Pluss Stauffer Ag | Verfahren und Vorrichtung für die Herstellung von Füllstoff- und/oder Pigmentsuspensionen insbesondere für die Papierindustrie sowie Pigmente für die Papierindustrie |
SI9200220A (en) | 1992-09-23 | 1994-03-31 | Sava Kranj | Fireproof material, process for their production and their use |
US5478550A (en) | 1992-11-06 | 1995-12-26 | Nippon Inorganic Colour & Chemical Co., Ltd. | Ultraviolet-shielding agent, method for the preparation thereof and cosmetic composition compounded therewith |
EP0602494B1 (en) * | 1992-12-10 | 1996-10-09 | Mitsubishi Paper Mills, Ltd. | Ink jet recording sheet |
WO1994022680A1 (en) | 1993-04-05 | 1994-10-13 | Exxon Chemical Patents Inc. | Composite tire inner-liners and inner tubes |
US5626945A (en) | 1993-09-28 | 1997-05-06 | International Paper Company | Repulpable, water repellant paperboard |
GB9320233D0 (en) * | 1993-10-01 | 1993-11-17 | Ecc Int Ltd | Paper coating pigment |
KR0169157B1 (ko) * | 1993-11-29 | 1999-02-01 | 기다오까 다까시 | 반도체 회로 및 mos-dram |
JPH07251486A (ja) | 1994-01-26 | 1995-10-03 | Sumitomo Chem Co Ltd | 積層フィルム |
SE9403857L (sv) | 1994-11-10 | 1996-05-11 | Peterson Seffle Ab | Fett-tätt och fettresistent omslagsmaterial |
GB2295617B (en) | 1994-12-03 | 1998-11-04 | Courtaulds Plc | Thermoplastic resin compositions and articles containing delaminated fillers |
WO1996022329A1 (en) | 1995-01-20 | 1996-07-25 | Le Groupe Recherche I.D. Inc. | Method and composition for providing repulpable moisture vapor barrier coating for flexible packaging |
US5645635A (en) | 1995-02-07 | 1997-07-08 | Engelhard Corporation | Delaminated kaolin pigments, their preparation and use in paper filling applications |
HUP0104321A3 (en) | 1995-06-23 | 2003-05-28 | Exxon Research Engineering Co | Latex, nanocomposite and production of latex containing nanocomposite |
US5593490A (en) * | 1995-06-26 | 1997-01-14 | Thiele Kaolin Company | Kaolin clay slurries having reduced viscosities and process for the manufacture thereof |
EP0764739B1 (en) | 1995-09-22 | 2001-01-24 | Oji Paper Co., Ltd. | Moisture-proof paper sheet |
GB2310215A (en) | 1995-10-13 | 1997-08-20 | Ecc Int Ltd | Coating composition |
JP3531314B2 (ja) | 1995-10-17 | 2004-05-31 | 王子製紙株式会社 | 防湿性紙 |
GB2306392B (en) | 1995-10-31 | 1999-01-27 | British United Shoe Machinery | Waterproof insole material |
DE69729320T2 (de) | 1996-03-04 | 2005-06-02 | Fp-Pigments Oy | Mit gefalltem calciumcarbonat beschichtete pigmentteilchen und verfahren zu deren herstellung |
US6312511B1 (en) | 1996-03-22 | 2001-11-06 | Imerys Kaolin, Inc. | Kaolin clays and methods of making and using same |
JP4033520B2 (ja) | 1996-08-12 | 2008-01-16 | ゼネラル・エレクトリック・カンパニイ | 難燃性ポリエステル組成物 |
JP3793297B2 (ja) * | 1996-11-01 | 2006-07-05 | デュポン株式会社 | 低密度ポリエチレン−層状珪酸塩複合材料およびその製造方法 |
DE19649444C2 (de) | 1996-11-28 | 1999-07-15 | Sphinx Elektronik Gmbh | Schloß |
BR9806759A (pt) | 1997-01-17 | 2000-03-14 | Eg Technology Partners | Composição, processo para a manufatura de um substrato tendo propriedades de barreira, e, recipiente de embalagem |
US5952093A (en) * | 1997-02-20 | 1999-09-14 | The Dow Chemical Company | Polymer composite comprising a inorganic layered material and a polymer matrix and a method for its preparation |
JP3169568B2 (ja) * | 1997-03-19 | 2001-05-28 | 筒中プラスチック工業株式会社 | 部分的に金属光沢を有する熱成形体 |
JPH10298358A (ja) | 1997-04-23 | 1998-11-10 | Mitsui Chem Inc | 樹脂成形体 |
FI102401B1 (fi) * | 1997-05-28 | 1998-11-30 | Raisio Chem Oy | Menetelmä transparentin ja läpäisevyyttä vähentävän pinnoitteen aikaansaamiseksi paperille tai kartongille sekä menetelmässä käytettävä päällystysaine |
FI980086L (fi) | 1997-05-28 | 1998-11-29 | Enso Oyj | Päällystetty kartonki, sen valmistusmenetelmä sekä siitä muodostetut astiat ja pakkaukset |
WO1998056861A1 (en) | 1997-06-09 | 1998-12-17 | Herberts Gmbh | Aqueous coating composition of a polymer and exfoliated platelet filler |
EP0991530B1 (en) | 1997-06-09 | 2004-09-22 | InMat, L.L.C. | Barrier coating of a polymer and a dispersed layered filler, a method of coatingparticles with said barrier coating and coated compositions, particulary tires. |
US6087016A (en) * | 1997-06-09 | 2000-07-11 | Inmat, Llc | Barrier coating of an elastomer and a dispersed layered filler in a liquid carrier |
US6232389B1 (en) | 1997-06-09 | 2001-05-15 | Inmat, Llc | Barrier coating of an elastomer and a dispersed layered filler in a liquid carrier and coated articles |
AU8139398A (en) | 1997-06-12 | 1998-12-30 | Ecc International Inc. | Filler composition for groundwood-containing grades of paper |
SE509536C2 (sv) | 1997-06-24 | 1999-02-08 | Moelnlycke Ab | Absorberande alster med förbättrad vätskemottagningsförmåga |
US6117541A (en) | 1997-07-02 | 2000-09-12 | Tetra Laval Holdings & Finance, Sa | Polyolefin material integrated with nanophase particles |
US5897411A (en) * | 1997-10-01 | 1999-04-27 | Reichhold Chemicals, Inc. | Repulpable moisture vapor barrier |
JP3941189B2 (ja) | 1997-10-29 | 2007-07-04 | 凸版印刷株式会社 | ガスバリア性紙製材料 |
JP3941188B2 (ja) | 1997-10-29 | 2007-07-04 | 凸版印刷株式会社 | ガスバリア性積層材料 |
FR2774689B1 (fr) | 1998-02-11 | 2001-05-04 | Nyltech Italia | Composition polyamide ignifugee |
US6358576B1 (en) * | 1998-02-12 | 2002-03-19 | International Paper Company | Clay-filled polymer barrier materials for food packaging applications |
WO1999043747A1 (en) | 1998-02-27 | 1999-09-02 | General Electric Company | Flame retardant polymer blends |
US6245395B1 (en) | 1998-03-02 | 2001-06-12 | Westvaco Corporation | Packaging material having good moisture barrier properties from C1S paperboard |
GB9807180D0 (en) * | 1998-04-04 | 1998-06-03 | Ecc Int Ltd | Pigment products |
AU3893199A (en) | 1998-05-11 | 1999-11-29 | Ecc International Inc. | Preparation and use of high brightness kaolin pigments |
US6402826B1 (en) * | 1998-11-30 | 2002-06-11 | Imerys Pigments, Inc. | Kaolin clay pigment for paper coating and method for producing same |
JP2000265391A (ja) | 1999-03-17 | 2000-09-26 | Oji Paper Co Ltd | 易離解性防湿紙 |
DE10084442T1 (de) | 1999-04-01 | 2002-05-02 | Imerys Pigments Inc | Kaolin-Pigmente, ihre Herstellung und Verwendung |
JP3634229B2 (ja) | 1999-04-02 | 2005-03-30 | 東洋紡績株式会社 | 無機強化ポリアミド樹脂組成物 |
JP2000303386A (ja) | 1999-04-19 | 2000-10-31 | Oji Paper Co Ltd | バリア性防湿積層体 |
ATE297959T1 (de) | 1999-04-30 | 2005-07-15 | Sued Chemie Ag | Flammhemmende zusammensetzungen |
CN1240587C (zh) | 1999-06-14 | 2006-02-08 | 国际纸业公司 | 多层树脂/纸层状结构以及由其制备的包装材料 |
EP1200254A1 (en) | 1999-06-17 | 2002-05-02 | Triton Systems Inc. | High performance nanocomposites |
US6554892B1 (en) * | 1999-07-02 | 2003-04-29 | Imerys Kaolin, Inc. | Compositions and methods for making a coarse platey, high brightness kaolin product |
JP3557950B2 (ja) | 1999-07-09 | 2004-08-25 | 王子製紙株式会社 | 防湿積層体 |
DE60033608T2 (de) | 1999-09-29 | 2007-11-22 | Toyo Boseki K.K. | Anorganisch verstärkte Polyamid-Harz-Zusammensetzungen |
JP2001098149A (ja) | 1999-09-29 | 2001-04-10 | Toyobo Co Ltd | ポリアミド樹脂組成物 |
AU2579001A (en) | 1999-12-21 | 2001-07-03 | Dow Chemical Company, The | Drip resistant polymer composition |
SE0000160L (sv) | 2000-01-18 | 2001-07-19 | Ecolean Ab | Återanvändbar behållare för vätskeformiga produkter samt metod för framställning därav |
FI107815B (fi) | 2000-02-11 | 2001-10-15 | Raisio Chem Oy | Päällystyspastakoostumus, sen käyttö ja menetelmä sen valmistamiseksi |
US6632868B2 (en) | 2000-03-01 | 2003-10-14 | Amcol International Corporation | Intercalates formed with polypropylene/maleic anhydride-modified polypropylene intercalants |
US6416817B1 (en) | 2000-03-03 | 2002-07-09 | Dow Corning Sa | Barrier coatings having bis-silanes |
AU2001238615A1 (en) | 2000-03-03 | 2001-09-17 | Dow Corning Corporation | Barrier coating compositions from amino functional silanes and phenolic compounds |
US6447845B1 (en) | 2000-03-03 | 2002-09-10 | Dow Corning Corporation | Barrier coatings using polyacids |
DE10010941A1 (de) | 2000-03-06 | 2001-09-13 | Bayer Ag | Flammwidrige Polycarbonat-Formmassen |
US6414070B1 (en) | 2000-03-08 | 2002-07-02 | Omnova Solutions Inc. | Flame resistant polyolefin compositions containing organically modified clay |
US6447860B1 (en) * | 2000-05-12 | 2002-09-10 | Pechiney Emballage Flexible Europe | Squeezable containers for flowable products having improved barrier and mechanical properties |
US6841211B1 (en) * | 2000-05-12 | 2005-01-11 | Pechiney Emballage Flexible Europe | Containers having improved barrier and mechanical properties |
GB0020179D0 (en) * | 2000-08-17 | 2000-10-04 | Imerys Minerals Ltd | Kaolin products and their use |
GB0020180D0 (en) | 2000-08-17 | 2000-10-04 | Imerys Minerals Ltd | Kaolin products and their production |
AU2001289119B2 (en) | 2000-09-21 | 2006-11-02 | Rohm And Haas Company | Aqueous nanocomposite dispersions:processes, compositions, and uses thereof |
WO2002024759A2 (en) | 2000-09-21 | 2002-03-28 | Rohm And Haas Company | Improved nanocomposite compositions and methods for making and using same |
DE10048059A1 (de) | 2000-09-28 | 2002-04-18 | Henkel Kgaa | Klebstoff mit Barriereeigenschaften |
US6916863B2 (en) * | 2000-11-14 | 2005-07-12 | Boral Material Technologies, Inc. | Filler comprising fly ash for use in polymer composites |
FR2822086B1 (fr) | 2001-03-13 | 2004-01-09 | Pechiney Emballage Flexible Eu | Procede de preparation d'une dispersion fluide nanocomposite et enduction nanocomposite correspondante |
AU783561B2 (en) | 2001-03-28 | 2005-11-10 | Oji Paper Co. Ltd. | Coated paper sheet |
JP2002363885A (ja) | 2001-03-28 | 2002-12-18 | Oji Paper Co Ltd | 塗工紙 |
US6623866B2 (en) | 2001-04-04 | 2003-09-23 | Exxonmobil Oil Corporation | Multilayer films including anti-block |
US20030085012A1 (en) * | 2001-09-07 | 2003-05-08 | Jones J Philip E | Hyperplaty clays and their use in paper coating and filling, methods for making same, and paper products having improved brightness |
US6673406B2 (en) | 2001-10-15 | 2004-01-06 | Cryovac, Inc. | High barrier polyvinylidene chloride composition and film |
JP3881547B2 (ja) | 2001-12-27 | 2007-02-14 | 株式会社クレハ | ポリ塩化ビニリデン系樹脂組成物、延伸フィルム、及びこれらの製造方法 |
US7135508B2 (en) | 2002-02-20 | 2006-11-14 | The University Of Chicago | Coatings and films derived from clay/wax nanocomposites |
US6790896B2 (en) | 2002-03-18 | 2004-09-14 | The University Of Chicago | Composite materials with improved phyllosilicate dispersion |
US6808559B2 (en) | 2002-02-26 | 2004-10-26 | Imerys Pigments, Inc. | Kaolin clay pigments suited to rotogravure printing applications and method for preparing the same |
JP2003292678A (ja) | 2002-04-05 | 2003-10-15 | Bridgestone Corp | ゴム組成物およびその製造方法 |
US6860924B2 (en) * | 2002-06-07 | 2005-03-01 | Nanoscale Materials, Inc. | Air-stable metal oxide nanoparticles |
US20040033379A1 (en) | 2002-06-12 | 2004-02-19 | Avery Dennison Corporation | Low permeability materials and coatings |
JP2004034390A (ja) | 2002-07-01 | 2004-02-05 | Nihon Tetra Pak Kk | 食品包装用樹脂組成物の製造法及び包装用積層体 |
US7935375B2 (en) | 2002-08-02 | 2011-05-03 | Basf Corporation | Process and coating composition for extending the shelf life of post harvest produce |
US6884450B2 (en) | 2002-10-03 | 2005-04-26 | Pactiv Corporation | Polypropylene containers |
US6864110B2 (en) | 2002-10-22 | 2005-03-08 | Agilent Technologies, Inc. | Electrophoretic processes for the selective deposition of materials on a semiconducting device |
AU2003295725A1 (en) | 2002-11-19 | 2004-06-15 | International Paper Company | Water vapor transmission rate resistant and repulpable corrugated paperboard |
US6942897B2 (en) | 2003-02-19 | 2005-09-13 | The Board Of Trustees Of Western Michigan University | Nanoparticle barrier-coated substrate and method for making the same |
US7320825B2 (en) | 2003-05-27 | 2008-01-22 | International Paper Company | Barrier coatings for oil and grease resistance |
US20040241482A1 (en) | 2003-06-02 | 2004-12-02 | Grah Michael D. | PVdC film with nanocomposite tie layer |
US20050037162A1 (en) | 2003-08-11 | 2005-02-17 | Adams John Peter | Paperboard laminate for food packaging applications |
US7473729B2 (en) | 2003-08-29 | 2009-01-06 | Inmat Inc. | Barrier coating mixtures containing non-elastomeric acrylic polymer with silicate filler and coated articles |
US8063119B2 (en) | 2003-08-29 | 2011-11-22 | Inmat Inc. | Barrier coating of a non-elastomeric polymer and a dispersed layered filler in a liquid carrier and coated articles |
US7078453B1 (en) | 2003-08-29 | 2006-07-18 | Inmat Inc. | Barrier coating of a non-butyl elastomer and a dispersed layered filler in a liquid carrier and coated articles |
JP2004003118A (ja) | 2003-09-01 | 2004-01-08 | Oji Paper Co Ltd | 防湿性紙 |
FR2862308B1 (fr) | 2003-11-14 | 2008-02-15 | Solvay | Procede de fabrication d'une resine synthetique et resine synthetique obtenue au moyen de ce procede |
US20050145138A1 (en) * | 2003-12-30 | 2005-07-07 | Council Of Scientific And Industrial Research | Oxygen barrier material for packaging |
JPWO2005108222A1 (ja) | 2004-05-07 | 2008-03-21 | テトラ ラバル ホールディングス アンド ファイナンス エス エイ | バリア性容器及びバリア性容器の製造法 |
-
2002
- 2002-09-04 US US10/233,599 patent/US20030085012A1/en not_active Abandoned
- 2002-09-06 BR BRPI0210811A patent/BR0210811B1/pt active IP Right Grant
- 2002-09-06 EP EP02757609.9A patent/EP1425351B1/en not_active Expired - Lifetime
- 2002-09-06 ES ES02757609.9T patent/ES2585882T3/es not_active Expired - Lifetime
- 2002-09-06 AU AU2002323615A patent/AU2002323615B2/en not_active Ceased
- 2002-09-06 BR BR122013002665A patent/BR122013002665B1/pt not_active IP Right Cessation
- 2002-09-06 CN CNA028175611A patent/CN1592770A/zh active Pending
- 2002-09-06 CA CA2920439A patent/CA2920439C/en not_active Expired - Lifetime
- 2002-09-06 EP EP10181338.4A patent/EP2280045B1/en not_active Expired - Lifetime
- 2002-09-06 WO PCT/US2002/028305 patent/WO2003022933A2/en active Application Filing
- 2002-09-06 ES ES10181338T patent/ES2809180T3/es not_active Expired - Lifetime
- 2002-09-06 JP JP2003527002A patent/JP5111720B2/ja not_active Expired - Lifetime
- 2002-09-06 CA CA2452563A patent/CA2452563C/en not_active Expired - Lifetime
-
2005
- 2005-03-23 US US11/086,563 patent/US7226005B2/en not_active Expired - Lifetime
- 2005-03-23 US US11/086,575 patent/US7208039B2/en not_active Expired - Lifetime
- 2005-04-19 US US11/108,878 patent/US7214264B2/en not_active Expired - Lifetime
Patent Citations (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2158987A (en) * | 1934-11-26 | 1939-05-16 | Georgia Kaolin Co | Clay product and process of preparing same |
US4125411A (en) * | 1958-09-30 | 1978-11-14 | Yara Engineering Corporation | Kaolin product |
US3034859A (en) * | 1959-04-27 | 1962-05-15 | Southern Clays Inc | Delaminated english clay products, etc. |
US3171718A (en) * | 1962-02-16 | 1965-03-02 | Freeport Sulphur Co | Delaminated domestic sedimentary clay products and method of preparation thereof |
US3526768A (en) * | 1964-03-06 | 1970-09-01 | Union Oil Co | 2-substituted naphth(1,2)oxazole scintillators |
US3615806A (en) * | 1968-12-10 | 1971-10-26 | Georgia Kaolin Co | Kaolin pigments and methods of producing the same |
US3635662A (en) * | 1969-12-05 | 1972-01-18 | Georgia Kaolin Co | Kaolin product and method of producing the same |
US4359497A (en) * | 1971-08-30 | 1982-11-16 | Princeton Chemical Research, Inc. | Paper-like butene-1 polymer compositions |
US4176148A (en) * | 1971-08-30 | 1979-11-27 | Princeton Chemical Research, Inc. | Method of manufacturing microporous paper-like butene-1 polymer sheets |
US3798044A (en) * | 1972-06-07 | 1974-03-19 | Huber Corp J M | Process for manufacturing calcined kaolinitic clay products |
US4221697A (en) * | 1974-05-29 | 1980-09-09 | Imperial Chemical Industries Limited | Composite materials |
US4251576A (en) * | 1974-05-29 | 1981-02-17 | Imperial Chemical Industries Limited | Inorganic reinforcing phase dispersed and bonded to polymer matrix |
US4234469A (en) * | 1976-07-29 | 1980-11-18 | Idemitsu Kosan Company Limited | Flame retarding polyolefin resin blend composition |
US4183991A (en) * | 1977-05-02 | 1980-01-15 | Rohm And Haas Company | Process for preparing highly filled acrylic articles |
US4225496A (en) * | 1977-07-27 | 1980-09-30 | Borden, Inc. | Acrylic latex cove base cement |
US4250077A (en) * | 1977-09-02 | 1981-02-10 | Bayer Aktiengesellschaft | Stable suspensions of inorganic fillers in organic polyhydroxyl compounds for polyurethane preparation |
US4198333A (en) * | 1977-09-02 | 1980-04-15 | Bayer Aktiengesellschaft | Stable suspensions of inorganic fillers in organic polyhydroxyl compounds containing completely or partially neutralized carboxyl groups |
US4227920A (en) * | 1978-07-18 | 1980-10-14 | Yara Engineering Corporation | Methods of clay benefication |
US4467057A (en) * | 1978-12-06 | 1984-08-21 | General Electric Company | Modified polyester composition |
US4241142A (en) * | 1978-12-20 | 1980-12-23 | Engelhard Minerals & Chemicals Corporation | Clay pigment for coating paper |
US4243574A (en) * | 1979-03-30 | 1981-01-06 | E. I. Du Pont De Nemours And Company | Poly(meta-phenylene isophthalamide) molding compositions |
US4414352A (en) * | 1979-05-01 | 1983-11-08 | General Electric Company | Thermoplastic molding compositions and process |
US4233199A (en) * | 1979-07-03 | 1980-11-11 | Visvaldis Abolins | Flame resistant thermoplastic compositions with well balanced physical properties |
US4381948A (en) * | 1979-07-26 | 1983-05-03 | Anglo-American Clays Corporation | Anhydrous kaolin clay pigment and method of preparation |
US4298711A (en) * | 1980-04-09 | 1981-11-03 | Cargill Incorporated | Low shrink unsaturated polyester resinous composition |
US4409344A (en) * | 1980-04-09 | 1983-10-11 | Cargill Incorporated | Low shrink unsaturated polyester resinous composition |
US4543287A (en) * | 1980-07-11 | 1985-09-24 | Imperial Chemical Industries Limited | Fibrous material comprised of vermiculte coated fibers |
US4427450A (en) * | 1980-08-04 | 1984-01-24 | Engelhard Corporation | Chalking-resistant, calcined kaolin clay pigment and method of making |
US4311635A (en) * | 1980-08-25 | 1982-01-19 | Pantasote Inc. | Flame resistant thermoplastic elastomer |
US4546126A (en) * | 1983-07-13 | 1985-10-08 | Ciba Geigy Corporation | Flame-retarding, reinforced moulding material based on thermoplastic polyesters and the use thereof |
US4820761A (en) * | 1983-07-19 | 1989-04-11 | Sumitomo Chemical Company, Limited | Aromatic polysulfone resin composition |
US4584333A (en) * | 1984-01-17 | 1986-04-22 | Les Cables De Lyon | Fire-resistant thermoplastic composition |
US4582866A (en) * | 1984-04-30 | 1986-04-15 | E. I. Du Pont De Nemours And Company | Flame retardant thermoplastic multi-block copolyester elastomers |
USRE37385E1 (en) * | 1985-09-30 | 2001-09-18 | Kabushiki Kaisha Toyoto Chuo Kenkyusho | Composite material and process for manufacturing same |
US4708975A (en) * | 1986-04-02 | 1987-11-24 | E. I. Du Pont De Nemours And Company | Low smoke generating, high char forming, flame retardant thermoplastic multi-block copolyesters |
US4888315A (en) * | 1986-06-04 | 1989-12-19 | Georgia Kaolin Company, Inc. | High solids blended kaolin clay slurry |
US4873116A (en) * | 1986-09-30 | 1989-10-10 | Union Carbide Chemicals And Plastics Company Inc. | Method of preparing mixtures of incompatible hydrocarbon polymers |
US4889886A (en) * | 1986-12-10 | 1989-12-26 | Polyplastics Co., Ltd. | Liquid crystal polyester composition |
US4918127A (en) * | 1986-12-31 | 1990-04-17 | Bp Performance Polymers, Inc. | Filled elastomer blends |
US4795776A (en) * | 1987-01-29 | 1989-01-03 | Dixon International Limited | Fire-resistant composition |
US5573946A (en) * | 1988-02-25 | 1996-11-12 | Pfizer Inc. | Biologically pure culture of Streptomyces hygroscopicus ATCC 53718 capable of producing antibiotic compounds |
US4981521A (en) * | 1988-05-09 | 1991-01-01 | W. R. Grace & Co.-Conn. | Sprayable fireproofing composition |
US5085707A (en) * | 1988-05-23 | 1992-02-04 | Georgia Kaolin Company, Inc. | Defined and delaminated kaolin product |
US4943324A (en) * | 1988-05-23 | 1990-07-24 | Georgia Kaolin Company, Inc. | High performance paper filler and method of producing same |
US5112782A (en) * | 1989-05-04 | 1992-05-12 | Engelhard Corporation | Cationically processed calcined kaolin clay |
US4966638A (en) * | 1989-06-13 | 1990-10-30 | Lestox, Inc. | Silicone mixture and method of using it |
US5128606A (en) * | 1990-01-22 | 1992-07-07 | Ecc International Limited | Aspect radio measurement |
US5168083A (en) * | 1990-05-09 | 1992-12-01 | Georgia Kaolin Company, Inc. | High opacity defined kaolin product and method of producing same |
US5416151A (en) * | 1990-09-14 | 1995-05-16 | Mitsui Petrochemical Industries, Ltd. | Polymer composition and its use |
US5167707A (en) * | 1991-03-29 | 1992-12-01 | J. M. Huber Corporation | High performance coarse particle size sams pigments for paint and plastics applications |
US5294654A (en) * | 1991-08-12 | 1994-03-15 | General Electric Company | Flame-retarded, conductive compositions which include polyphenylene ether and polystyrene resins |
US5411587A (en) * | 1991-11-13 | 1995-05-02 | Engelhard Corporation | Paper coating kaolin pigments their preparation and use |
US5169443A (en) * | 1991-11-13 | 1992-12-08 | Engelhard Corporation | Paper coating kaolin pigments there preparation and use |
US5364899A (en) * | 1992-01-24 | 1994-11-15 | Denki Kagaku Koguo Kabushiki Kaisha | Flame-retardant resin composition |
US5439558A (en) * | 1992-04-25 | 1995-08-08 | Stora Feldmuhle Ag | Print substrate |
US5332493A (en) * | 1992-04-28 | 1994-07-26 | Ecc International Inc. | Method for improving rheological properties of kaolin clays |
US5516829A (en) * | 1992-08-10 | 1996-05-14 | Davis; James A. | Heat seamable flame retardant roof sheeting with highly crystalline thermoplasticity promoters and method for covering roofs |
US6031036A (en) * | 1992-10-07 | 2000-02-29 | General Electric Company | Flame resistant thermoplastic blends having reduced drippage |
US5454865A (en) * | 1993-12-23 | 1995-10-03 | Ecc International Inc. | Method for preparing refined kaolin in clay products |
US5948156A (en) * | 1994-03-28 | 1999-09-07 | Sud-Chemie, Ag | Supplementary agent for mineral binder systems |
US5578659A (en) * | 1994-07-04 | 1996-11-26 | Polyplastics Co., Ltd. | Polyarylene sulfide resin composition |
US5749958A (en) * | 1995-02-07 | 1998-05-12 | Engelhard Corporation | Delaminated kaolin pigments their preparation and use in paper coating |
US5522924A (en) * | 1995-03-17 | 1996-06-04 | Ecc International Inc. | Method for producing high brightness low abrasion calcined kaolin pigment |
US5624488A (en) * | 1995-06-30 | 1997-04-29 | Engelhard Corporation | Ultrahigh brightness calcined clay pigment, manufacture & use thereof |
US5925454A (en) * | 1995-07-11 | 1999-07-20 | W.R. Grace & Co.-Conn. | Film having modified surface characteristics through use of combination of spherical and lamellar particulates |
US5646635A (en) * | 1995-08-17 | 1997-07-08 | Centurion International, Inc. | PCMCIA antenna for wireless communications |
US5879512A (en) * | 1995-10-13 | 1999-03-09 | Ecc Internatinal Ltd. | Paper coating |
US5685900A (en) * | 1995-10-18 | 1997-11-11 | Ecc International Inc. | Method for beneficiating discolored kaolin to produce high brightness coating clay |
US5707912A (en) * | 1996-03-18 | 1998-01-13 | Thiele Kaolin Company | Process for the treatment of clay materials to provide slurries having improved rheological properties |
US5735946A (en) * | 1996-05-14 | 1998-04-07 | U.S. Borax, Inc. | Two-stage process for delaminating kaolin |
US5846309A (en) * | 1997-02-20 | 1998-12-08 | J. M. Huber Corporation | Coarse particle size kaolin clay and method |
US5810998A (en) * | 1997-06-05 | 1998-09-22 | Thiele Kaolin Company | Process for improving the brightness of fine-grained kaolin clays |
US6262161B1 (en) * | 1997-06-26 | 2001-07-17 | The Dow Chemical Company | Compositions having improved ignition resistance |
US6186335B1 (en) * | 1998-03-20 | 2001-02-13 | Thiele Kaolin Company | Process for beneficiating kaolin clays |
US6149723A (en) * | 1998-07-22 | 2000-11-21 | Imerys Pigments, Inc. | Engineered kaolin pigment composition for paper coating |
US6564199B1 (en) * | 1999-04-01 | 2003-05-13 | Imerys Pigments, Inc. | Kaolin clay pigments, their preparation and use |
US6758895B2 (en) * | 2000-08-17 | 2004-07-06 | Imerys Minerals Limited | Particulate mineral materials |
US6402286B1 (en) * | 2001-02-09 | 2002-06-11 | Industrial Technology Research Institute | Function test device for optical print head heaters in thermal bubble printers |
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Also Published As
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US7214264B2 (en) | 2007-05-08 |
US20060009566A1 (en) | 2006-01-12 |
WO2003022933A3 (en) | 2003-08-21 |
EP1425351A2 (en) | 2004-06-09 |
US7226005B2 (en) | 2007-06-05 |
EP2280045B1 (en) | 2020-05-13 |
ES2809180T3 (es) | 2021-03-03 |
WO2003022933A2 (en) | 2003-03-20 |
CA2452563A1 (en) | 2003-03-20 |
CA2920439A1 (en) | 2003-03-20 |
US20050247418A1 (en) | 2005-11-10 |
BR122013002665B1 (pt) | 2016-02-16 |
US20060032405A2 (en) | 2006-02-16 |
CA2452563C (en) | 2016-04-26 |
EP2280045A2 (en) | 2011-02-02 |
ES2585882T3 (es) | 2016-10-10 |
AU2002323615B2 (en) | 2008-08-07 |
US20050178292A1 (en) | 2005-08-18 |
CA2920439C (en) | 2020-01-07 |
BR0210811B1 (pt) | 2016-12-13 |
CN1592770A (zh) | 2005-03-09 |
BR0210811A (pt) | 2004-06-22 |
EP2280045A3 (en) | 2011-06-08 |
EP1425351B1 (en) | 2016-05-11 |
US7208039B2 (en) | 2007-04-24 |
JP2005502758A (ja) | 2005-01-27 |
JP5111720B2 (ja) | 2013-01-09 |
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