WO2001000713A1 - Polymer pigment applicable in dry form - Google Patents

Polymer pigment applicable in dry form Download PDF

Info

Publication number
WO2001000713A1
WO2001000713A1 PCT/FI2000/000564 FI0000564W WO0100713A1 WO 2001000713 A1 WO2001000713 A1 WO 2001000713A1 FI 0000564 W FI0000564 W FI 0000564W WO 0100713 A1 WO0100713 A1 WO 0100713A1
Authority
WO
WIPO (PCT)
Prior art keywords
pigment
plastic
dry
applicable
paper
Prior art date
Application number
PCT/FI2000/000564
Other languages
French (fr)
Inventor
Mikael Skrifvars
Toivo Kärnä
Timo Nyberg
Kaisa Putkisto
Veli KÄSMÄ
Juha Maijala
Harri Vuolle
Original Assignee
Dynea Chemicals Oy
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FI991438A external-priority patent/FI991438A/en
Application filed by Dynea Chemicals Oy filed Critical Dynea Chemicals Oy
Priority to EA200200074A priority Critical patent/EA200200074A1/en
Priority to BR0011922-9A priority patent/BR0011922A/en
Priority to JP2001506720A priority patent/JP2003503606A/en
Priority to EP00940439A priority patent/EP1200508A1/en
Priority to CA002377231A priority patent/CA2377231A1/en
Priority to AU55376/00A priority patent/AU5537600A/en
Publication of WO2001000713A1 publication Critical patent/WO2001000713A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/03Printing inks characterised by features other than the chemical nature of the binder
    • C09D11/037Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/12Powdering or granulating
    • C08J3/16Powdering or granulating by coagulating dispersions
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/062Copolymers with monomers not covered by C09D133/06
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/65Additives macromolecular
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/66Additives characterised by particle size
    • C09D7/67Particle size smaller than 100 nm
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/66Additives characterised by particle size
    • C09D7/68Particle size between 100-1000 nm
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/66Additives characterised by particle size
    • C09D7/69Particle size larger than 1000 nm
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H19/00Coated paper; Coating material
    • D21H19/36Coatings with pigments
    • D21H19/38Coatings with pigments characterised by the pigments
    • D21H19/42Coatings with pigments characterised by the pigments at least partly organic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2325/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • C08J2325/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2333/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
    • C08J2333/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
    • C08J2333/06Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C08J2333/10Homopolymers or copolymers of methacrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/14Polymer mixtures characterised by other features containing polymeric additives characterised by shape
    • C08L2205/18Spheres
    • C08L2205/20Hollow spheres
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L25/00Compositions of, homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Compositions of derivatives of such polymers
    • C08L25/02Homopolymers or copolymers of hydrocarbons
    • C08L25/04Homopolymers or copolymers of styrene
    • C08L25/06Polystyrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L33/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • C08L33/04Homopolymers or copolymers of esters
    • C08L33/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
    • C08L33/10Homopolymers or copolymers of methacrylic acid esters
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP 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
    • D21H23/00Processes or apparatus for adding material to the pulp or to the paper
    • D21H23/02Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
    • D21H23/04Addition to the pulp; After-treatment of added substances in the pulp
    • D21H23/20Apparatus therefor

Definitions

  • the present invention relates to dry polymer pigments, particularly to plastic pigments applicable in dry form which pigments may be used in a dry coating method of paper and board, and to a method for producing polymer pigments applicable in dry form.
  • This invention is further directed to a method for dry coating of paper and board with a polymer pigment by ionic blasting, and to dry coated paper and board.
  • Synthetic plastic pigments are increasingly used in coating of paper, to partly or totally replace conventional inorganic pigments, such as calcium carbonate and kaolin.
  • Plastic pigments are commonly used as aqueous dispersions, i.e. latexes, with dry matter contents varying between 20 and 60 wt%.
  • Synthetic plastic pigments may either have a solid core, or they may be hollow. Chemically these plastic pigments are based on polyacrylate, polymethacrylate, or polystyrene, or the copolymers thereof and further pigments based on urea-formaldehyde and melamin-formaldehyde are used.
  • a plastic pigment, particularly a hollow particle pigment endows the product made thereof with opacity and brightness.
  • a problem related to the aqueous dispersions of plastic pigments is, however, limited storage stability, and solid polymer particles tend to settle on the bottom of the container during extended storage.
  • plastic pigments do not usually tolerate freezing and thawing, and the polymer pigment also coagulates easily when freezing. Accordingly, the storage temperature restricts the storage thereof.
  • the aqueous dispersions of plastic pigments are liable to microbial growth. For these reasons, a plastic pigment easily turns into a useless product.
  • the water content of the aqueous dispersions of plastic pigments being normally from 40 to 80 %, significant extra expenses are caused by the transportation of water.
  • Coating of paper is conventionally carried out by applying on a paper web a pigment dispersion or paste, typically containing from 30 to 40 % of water. Drying of the coated paper is an energy consuming process, since the water must be removed with for instance IR-dryers. This water pollutes the environment, and must accordingly be treated carefully before releasing it into surface waters. Moreover, the coating line of a paper machine with its paste kitchen is a relatively large unit requiring lots of space, and further, the coating line of a paper machine is a very significant investment.
  • the paste is applied onto the web without contacting it, by means of ionic blasting provided by high voltage, wherein the particles are charged by the ions formed by corona discharge. Thereafter, an electric field transfers the charged particles onto the paper web.
  • Many quality properties of the paper are also improved, since the paper substrate is no longer wetted and redryed.
  • An object of the present invention is a plastic polymer pigment applicable in dry form, a method for producing such a plastic polymer pigment, applicable in dry form, and the use of a plastic polymer pigment, applicable in dry form, in a method for dry coating of paper or board.
  • another object of the inven- tion is a method for dry coating of paper or board by ionic blasting with a polymer pigment, and dry coated paper or board.
  • the characteristic features of the plastic polymer pigment, applicable in dry form, the method for producing such a plastic polymer pigment, applicable in dry form, the use of a plastic polymer pigment, applicable in dry form, in a method for dry coating of paper or board, the method for dry coating of paper or board by ionic blasting with a polymer pigment, and the dry coated paper or board of the invention are presented in the claims.
  • paper and board may be coated with a dry coating method by using plastic polymer pigments applicable in dry form.
  • Plastic polymer pigments may be dryed with a suitable method, preferably by using spray drying technique to produce finely divided pigment powder.
  • Suit- able polymer pigments are at least plastic pigments based on polystyrene, polyacrylate, and polymethacrylate, poly(styrene-acrylate)copolymers, plastic pigments based on melamin-formaldehyde and urea-formaldehyde, or combinations thereof.
  • the plastic pigment is dryed from an aqueous dispersion having a dry matter content from 1 to 85 wt%, preferably from 5 to 60 wt%, by weight.
  • the particle size of the plastic pigment to be dryed is in the range of 10 - 2000 nm, preferably
  • the plastic pigment to be dryed is hydrophobic or hydrophilic, and it may contain various reactive groups allowing the modification of its properties.
  • the bulk density of the plastic pigment to be dryed is between 100 and 2000 g/1, and the glass transition temperature thereof is from 80 to 160 °C.
  • the plastic pigment may be either hollow or solid.
  • the polymer dispersion is pumped to a nozzle of a cyclone.
  • the nozzle may be stationary or rotating, and the dispersion is quickly heated therein by means of hot air, having a temperature from 150 to 250 °C.
  • the dispersion is then blown into the cyclone, wherein droplets are formed and at the same time, water is immediately evaporated.
  • the temperature in the cyclone is in the range of about 80 - 100 °C.
  • the dryed pigment powder is collected in the receptable of the cyclone. Any suitable spray drying apparatus may be used as the spray dryer.
  • the properties of the plastic pigment may further be modified in several ways, both chemically and physically.
  • rheological properties thereof may be controlled, including: a) the viscosity in the softening range, b) the elasticity that lowers the penetration and prevents excessive flowing, and c) the degree of crosslinking that influences the elasticity and viscosity.
  • Quick heating and compressing steps of the dry coating method also have a beneficial effect on the rheological and thermal properties of the plastic pigment.
  • the thermal resistance of the plastic pigment may preferably be improved with a melamin-formaldehyde or urea-formaldehyde treatment, the melting temperature may be modified, pressure resistance may be improved, and charging properties and printability may be adjusted as desired.
  • Both solid and liquid adjuvants and additives may be added to the dispersion before, and in some cases even after spray drying.
  • Granulating additives, adhesives, optical brighteners, latex, agent that modify the electrical properties, and other conventional additives for paper and board may be added to the dispersion.
  • Suitable granulating additives include carboxy methyl cellulose (CMC), polyvinyl alcohol (PVA), styrene butadiene latex (SBS), polyethylene wax (PE), the suitable amount of an additive being from 0,5 to 5 wt% of the dispersion.
  • Suitable binders of the coating include SBS and PVA. Suitable additives may be used to improve the brightness of the paper or board.
  • Antimicrobial additives may be used in the manufacture of antibacterial paper or liquid packaging board. Further, inorganic additives such as kaolin, talc, titanium dioxide, satin white, precipitated calcium carbonate (PCC), ground calcium carbonate (GCC) or like may be used, beneficially influencing the properties of the plastic pigment, including chemical, physi- cal, printing and economic features thereof. These additives may also be used to adjust the charging, binding, and powdering properties of the plastic pigment, as well as the handling properties thereof when transporting and transferring the material to the coating unit.
  • inorganic additives such as kaolin, talc, titanium dioxide, satin white, precipitated calcium carbonate (PCC), ground calcium carbonate (GCC) or like may be used, beneficially influencing the properties of the plastic pigment, including chemical, physi- cal, printing and economic features thereof.
  • PCC precipitated calcium carbonate
  • GCC ground calcium carbonate
  • the drying of the plastic pigment either as such or combined with additives results in finely divided pigment particle agglomerates in dry form, with a particle size between 1 and 500 ⁇ m, the dry matter content thereof being in the range of 85 - 100 %.
  • These pigment particle agglomerates consist of individual spherical pigment particles bonded together with electrostatic forces. These particles may be either hollow or solid.
  • the dryed plastic pigment powder may optionally be treated with a refiner wherein the structure is partly crushed thus increasing porosity and opacity.
  • a refiner wherein the structure is partly crushed thus increasing porosity and opacity.
  • dry plastic polymer pigment include the ease of transportation and storage, and resistance to temperature changes.
  • a plastic pigment for instance affects the printing properties as follows: a) printing quality is improved since the gloss and smoothness are improved and are more uniform throughout the surface, b) plastic pigment is favourable to the setting and stability of the printing ink, since the surface is not too porous and the ink does not penetrate too deeply into the paper, c) since the surface of the plastic pigment particles is not porous, the printing ink will not spread too much, or form blurred outlines, and d) with the plastic pigments, sufficient surface strenght for printing is attained.
  • the hollow structure yields the particle elasticity under compression, and thus the surface of the coating will be compressed more that its middle layer during calendering or like finishing step, and binding.
  • the hollow core of the particle endows the coating with opacity as the ability to scatter light improves, and a wide particle size distribution results in dense packing that leads to superior hid- ing power.
  • the optical properties of the product depend on the size, shape, and topology of the pigment particles and the distribution thereof, allowing the adjustment of gloss, smoothness, opacity, brightness and hiding power.
  • a polymer pigment to be stored in a dry form is not liable to microbial contamination, for instance to bacterial contamination in contrast to prior aqueous disper- sions.
  • the particle may be compressed without losing its hollow structure.
  • a respective effect may be provided by adjusting the hollow volume between 10 and
  • a pigment with a narrow size distribution is charged more uniformly than a pigment with a wide size distribution.
  • Hollow polymer pigments generally increase the stiffness of paper or board, and they have a high hiding power.
  • the plastic pigment also acts as a binder for an inorganic pigment thus improving the binding thereof, and the smoothness of the coating.
  • the hollow agglomerate structure of the plastic pigment is retained in the coating, the plastic pigment in- creasing the binding power of other coating materials.
  • the plastic pigment may improve the opacity of coating blends by preventing the agglomeration of mineral components and by uniformly distributing the pigment.
  • the structure and the large scattering area of the plastic pigment particles and agglomerates are favorable for attaining a high opacity and a sufficient brightness in a dry coating layer.
  • the amount of a polymer acting as an adhesive needed for a known pigment volume is lower. With the plastic pigment, the shade of the coated product may be adjusted as desired.
  • the plastic pigments may be considered acting as additives for finishing the paper surface, since they make the surface mode adjustable. Thus the undesired com- pression of the paper substrate under pressure decreases.
  • the weight of the coated paper may be decreases by using pigments with a lower density.
  • the fiber proportion of the paper sub- strate may respectively be increased, thus increasing the strenght of the paper.
  • a paper coated with a plastic pigment is lighter than conventional paper.
  • the efficiency of the coating unit may respectively be improved by increasing the speed.
  • an advantage of the finely divided plastic pigment coating is the fact that it shrinks less than film forming latexes of prior art after thermal treatment and binding.
  • the use of the plastic pigment applicable in dry form provides several advantages in dry coating in comparison to conventional inorganic pigments, including the fact that the plastic pigments softens at about 100 - 120 °C, and thus the plastic pigment applied is well bound to the paper substrate during calender- ing, typically carried out above the glass transition temperature of the plastic pigment. Because of this softening, no extra binder is needed. If necessary, the composition of the coating may be taylored as desired by using other additives and components with the plastic pigments, thus making a wide variety of plastic pigments available.
  • the properties of the plastic pigments may be chemi- cally modified and taylored as desired.
  • the paper coated with the plastic pigment may be recycled by burning, since it does not contain any nonburning inorganic matter, or the plastic pigment may be chemically separated from the paper.
  • a plastic pigment, applicable in dry form, was prepared by spray drying from a plastic pigment dispersion based on polyacrylate and polystyrene, having a dry matter content of 30 %, by weight.
  • the temperature of the nozzle of the cyclone was 160 °C, and the temperature in the cyclone was 80 °C.
  • a rotating nozzle was used in the cyclone, rotating at the speed of 30 000 rpm.
  • the particle size of the dry plastic pigment obtained was 60 ⁇ m, the density was 0.26 g/cm 3 , and the wa- ter content was 0.05 %, by weight.
  • the paper substrate used was a yellowish, rather coarse paper from mechanical pulp, having following characteristics: grammage about 70 g/m 2 thickness 120 - 124 ⁇ m
  • the plastic pigment powder was applied onto the paper substrate by ionic blasting. After application, the powder was irreversibly bound to the paper by thermal compression.
  • the temperatures used in binding were: 100 °C, 120 °C, 150 °C, 170 °C and 200 °C.
  • Linear loads of the calender used at control points were 3.4 kN/m, 6.8 kN/m and 13.7 kN/m.
  • the total numer of the control points made using this plastic pigment was 15.
  • the binding of the pigment with IR heating was studied, the temperature being in this case about 110 °C.
  • the tensile strenght, the tearing and burst resistances, smoothness, gloss, opacity, and brightness of the coated paper were tested after thermal compression.
  • the opacity and brightness increased significantly compared to the paper sub- strate at the temperature range of 100 - 150 °C. Above 150 °C the opacity and brightness were comparable to those of the paper substrate.
  • high printability values were obtained by binding the coating at a low temperature (100 °C) with a high linear load (13.7 kN/m), or by using IR heating (110 °C) with a low linear load (3.4 kN/m).
  • a plastic pigment applicable in dry form was prepared as described in Example 1.
  • the temperature of the nozzle was 210 °C.
  • the particle size of the dry plastic pigment obtained was 70 ⁇ m, its density was 0.30 g/cnr, and the water content was 0.05 %, by weight.
  • the paper substrate was coated as in Example 1.
  • the opacity increased significantly compared to the paper substrate at the temperature range of 100 - 150 °C. Above 150 °C, the opacity was comparable to that of the paper substrate.
  • the tensile strenght of the coated paper was on an average by 5 - 10 kN/m higher than that of the paper substrate, and the tensile strenght improved as the temperature rose. • IR heating improved the tensile strenght on an average by 5 kN/m.
  • high printability values were obtained by binding the coating at a low temperature (100 °C) with a high linear load (13.7 kN/m), or by using IR heating (110 °C) with low linear load (3.4 kN/m).
  • a plastic pigment applicable in dry form was prepared from a plastic pigment dispersion of polyacrylate-polystyrene, added with 10 %, by weight, of calcium carbonate (PCC). The drying was carried out as in Example 1. The particle size was 30 ⁇ m, and the water content was 0,05 %, by weight.
  • the coating was carried out as in Example 1.
  • the properties of the paper were as follows: • The grammage of the paper was by 15 - 20 g/m 2 higher than that of the paper substrate.
  • the tensile strenght of the coated paper increased on an average by 5 kN/m. • At lower temperatures, the gloss of the coated paper was lower that that of the paper substrate. As the temperature rose, the gloss was approximately 10 % higher than that of the paper substrate.
  • printability values were high for a sample bound at a high temperature (200 °C) using a medium linear load (6.8 kN/m).
  • a plastic pigment, applicable in dry form, was prepared from a plastic pigment dispersion of polyacrylate-polystyrene, added with 10 %, by weight, of titanium dioxide. The drying was carried out as in Example 1. The particle size was 27 ⁇ m, and the water content was 0,05 %, by weight.
  • the dry coating was carried out as in Example 1.
  • examples 1 - 4 the coated paper substrates were studied with SEM and stereo microscopy. The images obtained revealed that the resulting surface was very smooth due to the dense packing of the pigment agglomerates deforming under pressure.

Abstract

The invention relates to dry polymer pigments, particularly to plastic pigments applicable in dry form that may be used in a dry coating method of paper and board, and to a method for producing polymer pigments applicable in dry form. The plastic polymer pigment applicable in dry form comprises plastic pigment particles wherein the size of individual particles is from 10 to 2000 nm, the dry matter content of the plastic polymer pigment being from 85 to 100 wt% of the polymer pigment, and the individual plastic pigment particles form agglomerates having a size from 1 to 500 νm.

Description

Polymer pigment applicable in dry form
The present invention relates to dry polymer pigments, particularly to plastic pigments applicable in dry form which pigments may be used in a dry coating method of paper and board, and to a method for producing polymer pigments applicable in dry form. This invention is further directed to a method for dry coating of paper and board with a polymer pigment by ionic blasting, and to dry coated paper and board.
Synthetic plastic pigments are increasingly used in coating of paper, to partly or totally replace conventional inorganic pigments, such as calcium carbonate and kaolin. Plastic pigments are commonly used as aqueous dispersions, i.e. latexes, with dry matter contents varying between 20 and 60 wt%. Synthetic plastic pigments may either have a solid core, or they may be hollow. Chemically these plastic pigments are based on polyacrylate, polymethacrylate, or polystyrene, or the copolymers thereof and further pigments based on urea-formaldehyde and melamin-formaldehyde are used. A plastic pigment, particularly a hollow particle pigment endows the product made thereof with opacity and brightness. A problem related to the aqueous dispersions of plastic pigments is, however, limited storage stability, and solid polymer particles tend to settle on the bottom of the container during extended storage. Moreover, plastic pigments do not usually tolerate freezing and thawing, and the polymer pigment also coagulates easily when freezing. Accordingly, the storage temperature restricts the storage thereof. In addition, the aqueous dispersions of plastic pigments are liable to microbial growth. For these reasons, a plastic pigment easily turns into a useless product. The water content of the aqueous dispersions of plastic pigments being normally from 40 to 80 %, significant extra expenses are caused by the transportation of water. Coating of paper is conventionally carried out by applying on a paper web a pigment dispersion or paste, typically containing from 30 to 40 % of water. Drying of the coated paper is an energy consuming process, since the water must be removed with for instance IR-dryers. This water pollutes the environment, and must accordingly be treated carefully before releasing it into surface waters. Moreover, the coating line of a paper machine with its paste kitchen is a relatively large unit requiring lots of space, and further, the coating line of a paper machine is a very significant investment.
Recently, a new dry coating method by ionic blasting that saves water, energy, and raw materials has been developed for paper coating. Dry coated paper web needs no drying, and thus no energy is consumed by drying. Further, such a paper machine requires less space than a conventional one. In the new dry coating method, a dry pigment is applied onto a paper web using a particle transfer tech- nique based on ionic blasting. This method also utilizes the binding properties of small particles. By transferring the coating material in the form of very fine particles onto the surface of the web using ionic blasting, the particles may be made to bind to paper fibers and to each other directly, without an extra binder. In this method, the paste is applied onto the web without contacting it, by means of ionic blasting provided by high voltage, wherein the particles are charged by the ions formed by corona discharge. Thereafter, an electric field transfers the charged particles onto the paper web. Many quality properties of the paper are also improved, since the paper substrate is no longer wetted and redryed. The above teaching suggests that there is an evident need for a synthetic plastic pigment, applicable in dry form, that may particularly be used in the new dry coating method of paper.
An object of the present invention is a plastic polymer pigment applicable in dry form, a method for producing such a plastic polymer pigment, applicable in dry form, and the use of a plastic polymer pigment, applicable in dry form, in a method for dry coating of paper or board. In addition, another object of the inven- tion is a method for dry coating of paper or board by ionic blasting with a polymer pigment, and dry coated paper or board.
The characteristic features of the plastic polymer pigment, applicable in dry form, the method for producing such a plastic polymer pigment, applicable in dry form, the use of a plastic polymer pigment, applicable in dry form, in a method for dry coating of paper or board, the method for dry coating of paper or board by ionic blasting with a polymer pigment, and the dry coated paper or board of the invention are presented in the claims.
In the present invention, it was discovered that paper and board may be coated with a dry coating method by using plastic polymer pigments applicable in dry form. Plastic polymer pigments may be dryed with a suitable method, preferably by using spray drying technique to produce finely divided pigment powder. Suit- able polymer pigments are at least plastic pigments based on polystyrene, polyacrylate, and polymethacrylate, poly(styrene-acrylate)copolymers, plastic pigments based on melamin-formaldehyde and urea-formaldehyde, or combinations thereof. The plastic pigment is dryed from an aqueous dispersion having a dry matter content from 1 to 85 wt%, preferably from 5 to 60 wt%, by weight. The particle size of the plastic pigment to be dryed is in the range of 10 - 2000 nm, preferably
150 - 1000 nm. With respect to the surface structure, the plastic pigment to be dryed is hydrophobic or hydrophilic, and it may contain various reactive groups allowing the modification of its properties. The bulk density of the plastic pigment to be dryed is between 100 and 2000 g/1, and the glass transition temperature thereof is from 80 to 160 °C. With respect to its structure, the plastic pigment may be either hollow or solid. By polymerizing different relative amounts of monomer starting materials, shell hardness, softening temperature, binding power, abrasion resistance, printability, and of course, material costs of the pigment particle may be controlled. The drying is carried out with any suitable drying method that pro- duces dry and sufficiently finely divided pigment powder, preferably be means of spray drying. In a conventional spray drying method, the polymer dispersion is pumped to a nozzle of a cyclone. The nozzle may be stationary or rotating, and the dispersion is quickly heated therein by means of hot air, having a temperature from 150 to 250 °C. The dispersion is then blown into the cyclone, wherein droplets are formed and at the same time, water is immediately evaporated. Typically, the temperature in the cyclone is in the range of about 80 - 100 °C. The dryed pigment powder is collected in the receptable of the cyclone. Any suitable spray drying apparatus may be used as the spray dryer.
The properties of the plastic pigment may further be modified in several ways, both chemically and physically. By adjusting the molecular weight distribution of the plastic pigment, rheological properties thereof may be controlled, including: a) the viscosity in the softening range, b) the elasticity that lowers the penetration and prevents excessive flowing, and c) the degree of crosslinking that influences the elasticity and viscosity.
Quick heating and compressing steps of the dry coating method also have a beneficial effect on the rheological and thermal properties of the plastic pigment. The thermal resistance of the plastic pigment may preferably be improved with a melamin-formaldehyde or urea-formaldehyde treatment, the melting temperature may be modified, pressure resistance may be improved, and charging properties and printability may be adjusted as desired.
Both solid and liquid adjuvants and additives may be added to the dispersion before, and in some cases even after spray drying. Granulating additives, adhesives, optical brighteners, latex, agent that modify the electrical properties, and other conventional additives for paper and board may be added to the dispersion. Suitable granulating additives include carboxy methyl cellulose (CMC), polyvinyl alcohol (PVA), styrene butadiene latex (SBS), polyethylene wax (PE), the suitable amount of an additive being from 0,5 to 5 wt% of the dispersion. Suitable binders of the coating include SBS and PVA. Suitable additives may be used to improve the brightness of the paper or board. Antimicrobial additives may be used in the manufacture of antibacterial paper or liquid packaging board. Further, inorganic additives such as kaolin, talc, titanium dioxide, satin white, precipitated calcium carbonate (PCC), ground calcium carbonate (GCC) or like may be used, beneficially influencing the properties of the plastic pigment, including chemical, physi- cal, printing and economic features thereof. These additives may also be used to adjust the charging, binding, and powdering properties of the plastic pigment, as well as the handling properties thereof when transporting and transferring the material to the coating unit.
The drying of the plastic pigment either as such or combined with additives results in finely divided pigment particle agglomerates in dry form, with a particle size between 1 and 500 μm, the dry matter content thereof being in the range of 85 - 100 %. These pigment particle agglomerates consist of individual spherical pigment particles bonded together with electrostatic forces. These particles may be either hollow or solid.
Further, the dryed plastic pigment powder may optionally be treated with a refiner wherein the structure is partly crushed thus increasing porosity and opacity. By treating dry pigment in a high-power refiner, the electrical properties of the pig- ment are changed, which affects the binding of the pigment to the paper web.
Advantages of the dry plastic polymer pigment include the ease of transportation and storage, and resistance to temperature changes.
A plastic pigment for instance affects the printing properties as follows: a) printing quality is improved since the gloss and smoothness are improved and are more uniform throughout the surface, b) plastic pigment is favourable to the setting and stability of the printing ink, since the surface is not too porous and the ink does not penetrate too deeply into the paper, c) since the surface of the plastic pigment particles is not porous, the printing ink will not spread too much, or form blurred outlines, and d) with the plastic pigments, sufficient surface strenght for printing is attained.
The hollow structure yields the particle elasticity under compression, and thus the surface of the coating will be compressed more that its middle layer during calendering or like finishing step, and binding. Moreover, the hollow core of the particle endows the coating with opacity as the ability to scatter light improves, and a wide particle size distribution results in dense packing that leads to superior hid- ing power. The optical properties of the product depend on the size, shape, and topology of the pigment particles and the distribution thereof, allowing the adjustment of gloss, smoothness, opacity, brightness and hiding power. In addition, a polymer pigment to be stored in a dry form is not liable to microbial contamination, for instance to bacterial contamination in contrast to prior aqueous disper- sions. The shape of the pigment being spherical, the particle may be compressed without losing its hollow structure. The adjustment of the refractive index of the plastic pigment between 1.3 and 1.65, preferably between 1.6 and 1.65, results in a significant deviation from the refractive index of air (being 1), thus increasing the scattering power and providing the brightness with a slight bluish shade. A respective effect may be provided by adjusting the hollow volume between 10 and
80 %. Since the drying process is fast, the surface properties of the particle are not altered during this short exposure to high temperatures. Spray drying may change the electrical properties of the particles, thus improving the formation of agglomerates. A pigment with a narrow size distribution is charged more uniformly than a pigment with a wide size distribution. Hollow polymer pigments generally increase the stiffness of paper or board, and they have a high hiding power. The plastic pigment also acts as a binder for an inorganic pigment thus improving the binding thereof, and the smoothness of the coating. The hollow agglomerate structure of the plastic pigment is retained in the coating, the plastic pigment in- creasing the binding power of other coating materials. The plastic pigment may improve the opacity of coating blends by preventing the agglomeration of mineral components and by uniformly distributing the pigment. The structure and the large scattering area of the plastic pigment particles and agglomerates are favorable for attaining a high opacity and a sufficient brightness in a dry coating layer. In case of plastic pigments, the amount of a polymer acting as an adhesive needed for a known pigment volume is lower. With the plastic pigment, the shade of the coated product may be adjusted as desired.
The plastic pigments may be considered acting as additives for finishing the paper surface, since they make the surface mode adjustable. Thus the undesired com- pression of the paper substrate under pressure decreases.
In addition to the high bulk and stiffness attained, the weight of the coated paper may be decreases by using pigments with a lower density. By providing the desired coating thickness with a lighter layer, the fiber proportion of the paper sub- strate may respectively be increased, thus increasing the strenght of the paper.
Accordingly, a paper coated with a plastic pigment is lighter than conventional paper.
Since a high quality surface is provided at lower treatment temperatures and pres- sures, the calender cylinders are worn less. The efficiency of the coating unit may respectively be improved by increasing the speed.
In addition, an advantage of the finely divided plastic pigment coating is the fact that it shrinks less than film forming latexes of prior art after thermal treatment and binding.
Various traditional methods used in paper processing technology may be replaced with this novel dry coating method using the polymer pigment applicable in dry form, selected according to the application. Further, the use of the plastic pigment applicable in dry form provides several advantages in dry coating in comparison to conventional inorganic pigments, including the fact that the plastic pigments softens at about 100 - 120 °C, and thus the plastic pigment applied is well bound to the paper substrate during calender- ing, typically carried out above the glass transition temperature of the plastic pigment. Because of this softening, no extra binder is needed. If necessary, the composition of the coating may be taylored as desired by using other additives and components with the plastic pigments, thus making a wide variety of plastic pigments available. Moreover, the properties of the plastic pigments may be chemi- cally modified and taylored as desired. The paper coated with the plastic pigment may be recycled by burning, since it does not contain any nonburning inorganic matter, or the plastic pigment may be chemically separated from the paper.
The invention will now be illustrated with the examples without wishing to limit the scope thereof.
Example 1
A plastic pigment, applicable in dry form, was prepared by spray drying from a plastic pigment dispersion based on polyacrylate and polystyrene, having a dry matter content of 30 %, by weight. The temperature of the nozzle of the cyclone was 160 °C, and the temperature in the cyclone was 80 °C. A rotating nozzle was used in the cyclone, rotating at the speed of 30 000 rpm. The particle size of the dry plastic pigment obtained was 60 μm, the density was 0.26 g/cm3, and the wa- ter content was 0.05 %, by weight.
The paper substrate used was a yellowish, rather coarse paper from mechanical pulp, having following characteristics: grammage about 70 g/m2 thickness 120 - 124 μm
Bendtsen smoothness 4.5 - 5 μm tearing resistance 400 mN burst index 2.0 tensile strenght machine direction 50 kN/m cross direction 25 kN/m opacity 94.1 brightness 90.1 gloss (75°) 8
The plastic pigment powder was applied onto the paper substrate by ionic blasting. After application, the powder was irreversibly bound to the paper by thermal compression. The temperatures used in binding were: 100 °C, 120 °C, 150 °C, 170 °C and 200 °C.
Linear loads of the calender used at control points were 3.4 kN/m, 6.8 kN/m and 13.7 kN/m. The total numer of the control points made using this plastic pigment was 15. In addition, the binding of the pigment with IR heating was studied, the temperature being in this case about 110 °C.
The tensile strenght, the tearing and burst resistances, smoothness, gloss, opacity, and brightness of the coated paper were tested after thermal compression.
The properties were as follows:
• The grammage of the paper increased only by about 10 - 15 g/m2.
• The thickness of the paper increased even by 10 - 20 μm.
• The smoothness of the paper improved by about 2.5 - 3 μm.
• The opacity and brightness increased significantly compared to the paper sub- strate at the temperature range of 100 - 150 °C. Above 150 °C the opacity and brightness were comparable to those of the paper substrate.
• The tensile strenght increased on an average by 5 kN/m, the effect being strongest at high temperatures. • The gloss increased with increasing temperatures. At lower temperatures, the gloss was lower than that of the paper substrate, and at higher temperatures the value of the gloss was approximately 15 % higher.
According to the IGT testing method, high printability values were obtained by binding the coating at a low temperature (100 °C) with a high linear load (13.7 kN/m), or by using IR heating (110 °C) with a low linear load (3.4 kN/m).
Example 2
A plastic pigment applicable in dry form was prepared as described in Example 1. The temperature of the nozzle was 210 °C. The particle size of the dry plastic pigment obtained was 70 μm, its density was 0.30 g/cnr, and the water content was 0.05 %, by weight.
The paper substrate was coated as in Example 1.
After the thermal compression, the properties of the paper were as follows:
• The grammage of the paper increased only by about 10 g/m2. • The thickness increased on an average even by 20 μm, at higher temperatures, the thickness of the coated paper decreased.
• The smoothness of the paper was improved by about 1.5 μm, and the smoothness of the coated paper improved as the temperature rose.
• The opacity increased significantly compared to the paper substrate at the temperature range of 100 - 150 °C. Above 150 °C, the opacity was comparable to that of the paper substrate.
• The brightness of the coated paper attained that of the paper substrate at temperatures above 150 °C.
• The tensile strenght of the coated paper was on an average by 5 - 10 kN/m higher than that of the paper substrate, and the tensile strenght improved as the temperature rose. • IR heating improved the tensile strenght on an average by 5 kN/m.
• The gloss of the paper coated at lower temperatures was comparable to that of the paper substrate, and as the temperature rose, the gloss improved significantly, being finally 20 % higher than that of the paper substrate.
According to the IGT testing method, high printability values were obtained by binding the coating at a low temperature (100 °C) with a high linear load (13.7 kN/m), or by using IR heating (110 °C) with low linear load (3.4 kN/m).
Example 3
A plastic pigment applicable in dry form was prepared from a plastic pigment dispersion of polyacrylate-polystyrene, added with 10 %, by weight, of calcium carbonate (PCC). The drying was carried out as in Example 1. The particle size was 30 μm, and the water content was 0,05 %, by weight.
The coating was carried out as in Example 1.
After the thermal compression, the properties of the paper were as follows: • The grammage of the paper was by 15 - 20 g/m2 higher than that of the paper substrate.
• The thickness of the paper increased even by 25 - 35 μm.
• The smoothness improved by 1.0 - 2.5 μm as the temperature rose.
• The opacity decreased as the temperature rose, being, however, higher than that of the paper substrate regardless of the temperature.
• The brightness was some percent higher than that of the paper substrate. As the temperature rose to its maximum value, the brightness reached the value of the paper substrate.
• The tensile strenght of the coated paper increased on an average by 5 kN/m. • At lower temperatures, the gloss of the coated paper was lower that that of the paper substrate. As the temperature rose, the gloss was approximately 10 % higher than that of the paper substrate.
According to the IGT testing method, printability values were high for a sample bound at a high temperature (200 °C) using a medium linear load (6.8 kN/m).
Example 4
A plastic pigment, applicable in dry form, was prepared from a plastic pigment dispersion of polyacrylate-polystyrene, added with 10 %, by weight, of titanium dioxide. The drying was carried out as in Example 1. The particle size was 27 μm, and the water content was 0,05 %, by weight.
The dry coating was carried out as in Example 1.
After the thermal compression, the properties of the paper were as follows:
• The grammage of the paper increased by 40 - 50 g/m .
• The thickness increased by 50 μm. • The smoothness of the coated paper improved by about 1.5 - 2.5 μm.
• The temperature had little effect on the opacity. The opacity of the coated paper was 3 % higher than that of the paper substrate.
• The opacity of an IR heated coated paper was 4 % higher than that of the paper substrate. • The brightness decreased with increasing temperatures, reaching however always higher values than those of the paper substrate, even as IR heating was used.
• The tensile strenght decreased with increasing temperatures. The lowest value thereof was however higher than that of the paper substrate, being on an aver- age by 5 - 10 kN/m higher.
• With IR heating, the tensile strength improved by 5 kN/m. • The gloss of the coated paper increased by about 10 %.
• The gloss of the IR heated coated paper was higher than that of the paper substrate at low pressures.
Example 5
In examples 1 - 4, the coated paper substrates were studied with SEM and stereo microscopy. The images obtained revealed that the resulting surface was very smooth due to the dense packing of the pigment agglomerates deforming under pressure.

Claims

Claims
1. A plastic polymer pigment, applicable in dry form, characterized in that the plastic polymer pigment comprises plastic pigment particles, the size of individual particles being from 10 to 2000 nm, and the dry matter content of the plastic polymer pigment being from 85 - 100 %, by weight.
2. A plastic polymer pigment of claim 1, applicable in dry form, characterized in that the individual plastic pigment particles form agglomerates having a size from l to 500 μm.
3. A plastic polymer pigment of claim 1 or 2, applicable in dry form, characterized in that the individual plastic pigment particles are hollow.
4. A plastic polymer pigment of claim 1 or 2, applicable in dry form, characterized in that the individual plastic pigment particles are solid.
5. A plastic polymer pigment of any of claims 1 - 4, applicable in dry form, characterized in that the refractive index of the plastic pigment is between 1.3 and 1.65, preferably between 1.6 and 1.65.
6. A plastic polymer pigment of any of claims 1 - 5, applicable in dry form, characterized in that the individual plastic pigment particles are bonded together with electrostatic forces to form agglomerates.
7. A plastic polymer pigment of any of claims 1 - 6, applicable in dry form, characterized in that the plastic pigment comprises a polymer based on polystyrene, polyacrylate, poly(styrene-acrylate), or polymethacrylate, or a polymer based on urea- formaldehyde or melamin-formaldehyde, or combinations thereof.
8. A plastic polymer pigment of any of claims 1 - 7, applicable in dry form, characterized in that the plastic pigment is modified with melamin-formaldehyde or urea- formaldehyde, or with combinations thereof.
9. A plastic polymer pigment of any of claims 1 - 8, applicable in dry form, characterized in that the plastic pigment further comprises a binder.
10. A plastic polymer pigment of any of claims 1 - 9, applicable in dry form, characterized in that the plastic pigment further comprises an inorganic pigment.
11. A plastic polymer pigment of any of claims 1 - 10, applicable in dry form, characterized in that the plastic pigment further comprises a granulating agent.
12. A plastic polymer pigment of any of claims 1 - 11, applicable in dry form, characterized in that the plastic pigment further comprises an additive used in the production of paper or board.
13. A plastic polymer pigment of any of claims 1 - 12, applicable in dry form, characterized in that the structure and the large scattering area of the plastic pig- ment particles and agglomerates are favorable for attaining a high opacity and a sufficient brightness in a dry coating layer, and the shade of the coated product is adjusted as desired with the plastic pigment.
14. A plastic polymer pigment of any of claims 1 - 13, applicable in dry form, characterized in that the properties needed in dry coating with the plastic pigment, including grounding and charging properties, adhesion to paper, ease of transfer with ionic blasting, and stability of the finely divided form in the process may be adjusted as desired.
15. A method for producing a plastic polymer pigment, applicable in dry form, characterized in that an aqueous dispersion of a plastic polymer pigment with a dry matter content of 1 - 85 %, the particle size of an individual plastic pigment particle being from 10 - 2000 nm, is dryed.
16. A method of claim 15, characterized in that the aqueous dispersion of a plas- tic polymer pigment is dryed by spray drying.
17. A method of claim 15 or 16, characterized in that the plastic pigment particle is hollow or solid.
18. A method of any of claims 15 - 17, characterized in that after drying, the plastic polymer pigment is ground, preferably with a high-power refiner.
19. A method of any of claims 15 - 18, characterized in that as a result of the drying, a finely divided powder is obtained with a particle size of 1 - 500 μm, and dry matter content of 85 - 100 %.
20. Use of the dry plastic polymer pigment according to any of claims 1 - 14, or the plastic polymer pigment produced with the method of any of the claims 15 - 19, in a method for dry coating of paper or board.
21. Use of claim 20, characterized in that the dry coating method is based on ionic blasting.
22. A method for dry coating of paper or board, characterized in that a paper or board web is coated by ionic blasting with a pigment or pigment mixture in the form of small particles, this pigment containing plastic polymer pigment wherein the particle size of the individual particles is from 10 to 2000 nm, the dry matter content of the pigment being from 85 to 100 wt%.
23. A method of claim 22, characterized in that the individual plastic pigment particles form agglomerates having a size from 1 to 500 μm.
24. A method of claim 22 or 23, characterized in that the individual plastic pigment particles are hollow.
25. A method of claim 22 or 23, characterized in that the individual plastic pigment particles are solid.
26. A method of any of claims 22 - 25, characterized in that the refractive index of the plastic pigment is between 1.3 and 1.65, preferably between 1.6 and 1.65.
27. A method of any of claims 22 - 26, characterized in that the individual plastic pigment particles are bonded together with electrostatic forces to form agglomerates.
28. A method of any of claims 22 - 27, characterized in that the plastic pigment comprises a polymer based on polystyrene, polyacrylate, poly(styrene-acrylate), or polymethacrylate, or a polymer based on urea-formaldehyde or melamin- formaldehyde, or combinations thereof.
29. A method of any of claims 22 - 28, characterized in that the plastic pigment is modified with melamin-formaldehyde or urea-formaldehyde, or with combinations thereof.
30. A method of any of claims 22 - 24, characterized in that the plastic pigment further comprises a binder.
31. A method of any of claims 22 - 30, characterized in that the plastic pigment further comprises an inorganic pigment.
32. A method of any of claims 22 - 31, characterized in that the plastic pigment further comprises a granulating agent.
33. A method of any of claims 22 - 32, characterized in that the plastic pigment further comprises an additive used in the production of paper or board.
34. A method of any of claims 22 - 33, characterized in that the structure and the large scattering area of the plastic pigment particles and agglomerates are favorable for attaining a high opacity and a sufficient brightness in a dry coating layer, and the shade of the coated product is adjusted as desired with the plastic pigment.
35. A method of any of claims 22 - 34, characterized in that the properties needed in dry coating with the plastic pigment, including grounding and charging properties, adhesion to paper, ease of transfer with ionic blasting, and stability of the finely divided form in the process may be adjusted as desired.
36. Dry coated paper or board, characterized in that it contains a plastic polymer pigment of any of claims 1 - 14 applicable in dry form.
PCT/FI2000/000564 1999-06-24 2000-06-22 Polymer pigment applicable in dry form WO2001000713A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
EA200200074A EA200200074A1 (en) 1999-06-24 2000-06-22 POLYMER PIGMENT APPLICABLE IN DRY APPEARANCE
BR0011922-9A BR0011922A (en) 1999-06-24 2000-06-22 Polymer pigment applicable in dry form
JP2001506720A JP2003503606A (en) 1999-06-24 2000-06-22 Polymer pigment applicable to dry form
EP00940439A EP1200508A1 (en) 1999-06-24 2000-06-22 Polymer pigment applicable in dry form
CA002377231A CA2377231A1 (en) 1999-06-24 2000-06-22 Polymer pigment applicable in dry form
AU55376/00A AU5537600A (en) 1999-06-24 2000-06-22 Polymer pigment applicable in dry form

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FI991438A FI991438A (en) 1999-06-24 1999-06-24 Organic pigment granulate for paper coating
FI991438 1999-06-24
FI19991742 1999-08-17
FI991742A FI19991742A (en) 1999-06-24 1999-08-17 In dry applicable polymer pigment

Publications (1)

Publication Number Publication Date
WO2001000713A1 true WO2001000713A1 (en) 2001-01-04

Family

ID=26160757

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/FI2000/000564 WO2001000713A1 (en) 1999-06-24 2000-06-22 Polymer pigment applicable in dry form

Country Status (9)

Country Link
EP (1) EP1200508A1 (en)
JP (1) JP2003503606A (en)
CN (1) CN1358210A (en)
AU (1) AU5537600A (en)
BR (1) BR0011922A (en)
CA (1) CA2377231A1 (en)
EA (1) EA200200074A1 (en)
FI (1) FI19991742A (en)
WO (1) WO2001000713A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001090260A2 (en) * 2000-05-19 2001-11-29 Ppg Industries Ohio, Inc. Coating compositions comprised of a geometrically ordered array of unfused polymeric particles, composition exhibiting bragg diffraction, and a method for inhibiting sound transmission
WO2002045869A1 (en) 2000-12-07 2002-06-13 Metso Paper, Inc. Method and use of a method for the dry application of barrier and adhesive materiels on webs
WO2006008657A2 (en) 2004-07-13 2006-01-26 Omya Development Ag Method for producing pigmentary particles that are self-binding, dry, or in an aqueous suspension or dispersion, and contain inorganic materials and binding agents
WO2006050871A2 (en) * 2004-11-12 2006-05-18 Basf Aktiengesellschaft Aqueous paper coating slip containing pigment-polymer hybrids
WO2006050873A1 (en) * 2004-11-12 2006-05-18 Basf Aktiengesellschaft Paper coating slip based on pigment-polymer hybrids
EP2447328A1 (en) 2010-10-29 2012-05-02 Omya Development AG Method for improving handleability of calcium carbonate containing materials

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FI121087B (en) * 2002-11-14 2010-06-30 Metso Paper Inc Coating procedure
CN109942844A (en) * 2019-03-29 2019-06-28 广东榕泰实业股份有限公司 A kind of aminoplast reconstruction grain production technology and process units

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4087581A (en) * 1974-09-23 1978-05-02 Champion International Corporation Opacifying super-particles
US4582756A (en) * 1983-07-12 1986-04-15 Matsumoto Yushi-Seiyaku Co., Ltd. Organic microballoon
GB2175591A (en) * 1985-05-09 1986-12-03 Mitsubishi Rayon Co Fine powder of an acrylonitrile-type polymer and method for its production
US4997870A (en) * 1988-11-25 1991-03-05 Wacker-Chemie Gmbh Process for the preparation of polyvinyl alcohols which are soluble in cold water and have been absorbed onto pigments
US5279708A (en) * 1990-08-03 1994-01-18 Imperial Chemical Industries Plc Spray drying process with spinning atomizer
JPH07233303A (en) * 1994-02-23 1995-09-05 Mitsubishi Rayon Co Ltd Acrylic polymer particle and acrylic sol using the same
EP0751192A1 (en) * 1994-03-15 1997-01-02 Nippon Carbide Kogyo Kabushiki Kaisha Powder paint, method of manufacturing the same, and method of painting using the paint
WO1999002572A1 (en) * 1997-07-07 1999-01-21 Shin Dai-Ichi Vinyl Corporation Vinyl chloride resin granules for paste processing and process for producing the same

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4087581A (en) * 1974-09-23 1978-05-02 Champion International Corporation Opacifying super-particles
US4582756A (en) * 1983-07-12 1986-04-15 Matsumoto Yushi-Seiyaku Co., Ltd. Organic microballoon
GB2175591A (en) * 1985-05-09 1986-12-03 Mitsubishi Rayon Co Fine powder of an acrylonitrile-type polymer and method for its production
US4997870A (en) * 1988-11-25 1991-03-05 Wacker-Chemie Gmbh Process for the preparation of polyvinyl alcohols which are soluble in cold water and have been absorbed onto pigments
US5279708A (en) * 1990-08-03 1994-01-18 Imperial Chemical Industries Plc Spray drying process with spinning atomizer
JPH07233303A (en) * 1994-02-23 1995-09-05 Mitsubishi Rayon Co Ltd Acrylic polymer particle and acrylic sol using the same
EP0751192A1 (en) * 1994-03-15 1997-01-02 Nippon Carbide Kogyo Kabushiki Kaisha Powder paint, method of manufacturing the same, and method of painting using the paint
WO1999002572A1 (en) * 1997-07-07 1999-01-21 Shin Dai-Ichi Vinyl Corporation Vinyl chloride resin granules for paste processing and process for producing the same

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 199609, Derwent World Patents Index; AN 1996-080106, XP002951406, MITSUBISHI RAYON CO LTD: "Acrylic polymer particles prodn. for acrylic sols - by emulsion polymerising acrylic monomer and spray drying emulsion obtd." *
DATABASE WPI Week 199910, Derwent World Patents Index; AN 1999-120793, XP002951405, SHIN DAI-ICHI VINYL CORP: "Vinyl chloride resin granules for paste processing - produced by spray-drying aqueous vinyl chloride polymer dispersion with removal of fine particles" *

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7217746B2 (en) 2000-05-19 2007-05-15 Ppg Industries Ohio, Inc. Coating compositions having a geometrically ordered array of polymeric particles and substrates coated therewith
WO2001090260A3 (en) * 2000-05-19 2002-06-13 Ppg Ind Ohio Inc Coating compositions comprised of a geometrically ordered array of unfused polymeric particles, composition exhibiting bragg diffraction, and a method for inhibiting sound transmission
WO2001090260A2 (en) * 2000-05-19 2001-11-29 Ppg Industries Ohio, Inc. Coating compositions comprised of a geometrically ordered array of unfused polymeric particles, composition exhibiting bragg diffraction, and a method for inhibiting sound transmission
WO2002045869A1 (en) 2000-12-07 2002-06-13 Metso Paper, Inc. Method and use of a method for the dry application of barrier and adhesive materiels on webs
EP1409152B1 (en) * 2000-12-07 2009-07-29 Metso Paper, Inc. Method and use of a method for the dry application of barrier and adhesive materiels on webs
WO2006008657A2 (en) 2004-07-13 2006-01-26 Omya Development Ag Method for producing pigmentary particles that are self-binding, dry, or in an aqueous suspension or dispersion, and contain inorganic materials and binding agents
WO2006050871A2 (en) * 2004-11-12 2006-05-18 Basf Aktiengesellschaft Aqueous paper coating slip containing pigment-polymer hybrids
WO2006050871A3 (en) * 2004-11-12 2006-07-06 Basf Ag Aqueous paper coating slip containing pigment-polymer hybrids
WO2006050873A1 (en) * 2004-11-12 2006-05-18 Basf Aktiengesellschaft Paper coating slip based on pigment-polymer hybrids
AU2005303977B2 (en) * 2004-11-12 2010-05-13 Omya International Ag Aqueous paper coating slip containing pigment-polymer hybrids
US7858154B2 (en) 2004-11-12 2010-12-28 Basf Aktiengesellschaft Paper coating slip based on pigment-polymer hybrids
EP2447328A1 (en) 2010-10-29 2012-05-02 Omya Development AG Method for improving handleability of calcium carbonate containing materials
WO2012055739A1 (en) 2010-10-29 2012-05-03 Omya Development Ag Method for improving handleability of calcium carbonate containing materials
US8999055B2 (en) 2010-10-29 2015-04-07 Omya International Ag Method for improving handleability of calcium carbonate containing materials
US9243122B2 (en) 2010-10-29 2016-01-26 Omya International Ag Method for improving handleability of calcium carbonate containing materials
EP3284789A1 (en) 2010-10-29 2018-02-21 Omya International AG Method for improving handleability of calcium carbonate containing materials

Also Published As

Publication number Publication date
EA200200074A1 (en) 2002-04-25
BR0011922A (en) 2002-03-19
CA2377231A1 (en) 2001-01-04
CN1358210A (en) 2002-07-10
FI19991742A (en) 2000-12-24
AU5537600A (en) 2001-01-31
JP2003503606A (en) 2003-01-28
EP1200508A1 (en) 2002-05-02

Similar Documents

Publication Publication Date Title
KR101861529B1 (en) Cellulose-reinforced high mineral content products and methods of making the same
EP0410678B1 (en) Process for the surface enhancement of articles of fibre reinforced plastics material
CA1044538A (en) Method of finishing coated paper
CA2305115C (en) High gloss coated paper
KR19990087473A (en) Pigment particles coated with precipitated calcium carbonate and preparation method thereof
WO2001000713A1 (en) Polymer pigment applicable in dry form
US3963843A (en) Production of coated paper
WO2005044469A1 (en) Recyclable repulpable coated paper stock
FI93477B (en) Improved paper coating mixture
JP5535419B2 (en) Pigment complex and method for producing the same
EP0842992B1 (en) Low gloss coating composition
JP2005520949A (en) Fiber web and method for producing the same
US4308320A (en) Method for coating and drying paper
EP0702737B1 (en) Treatment of cellulosic materials
Rennel et al. Consolidation behaviour and gloss of paper coatings based on plastic pigments
Rigdahl et al. Heterogeneous latices as binders in porous particle structures
JP2899771B2 (en) Production method of double-sided cast coated paper
Abhari Application of Suspension-polymerized Latexes in Surface Sizing and Pigment Coating of Paper
AU644754B2 (en) A granular filler for use in a process for the surface enhancement of articles of reinforced plastics material
Skeppstedt et al. Use of a polymer-treated mineral pigment in paper coatings
KR20190042163A (en) Preparing method of coated paper using nanolatex for size press coating
Finch Applications of latices in the paper industry
JPH08226095A (en) Production of cast coated paper

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 00809371.7

Country of ref document: CN

AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CR CU CZ DE DK DM DZ EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG US UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2000940439

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 55376/00

Country of ref document: AU

WWE Wipo information: entry into national phase

Ref document number: 2377231

Country of ref document: CA

ENP Entry into the national phase

Ref document number: 2001 506720

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 200200074

Country of ref document: EA

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWP Wipo information: published in national office

Ref document number: 2000940439

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 10019333

Country of ref document: US

WWW Wipo information: withdrawn in national office

Ref document number: 2000940439

Country of ref document: EP

REG Reference to national code

Ref country code: PT

Ref legal event code: MM4A

Effective date: 20060410