EP1960601B2 - Procede de fabrication de papier - Google Patents

Procede de fabrication de papier Download PDF

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Publication number
EP1960601B2
EP1960601B2 EP06813086.3A EP06813086A EP1960601B2 EP 1960601 B2 EP1960601 B2 EP 1960601B2 EP 06813086 A EP06813086 A EP 06813086A EP 1960601 B2 EP1960601 B2 EP 1960601B2
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EP
European Patent Office
Prior art keywords
polymer
colloidal particles
process according
cationic
colloidal
Prior art date
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Not-in-force
Application number
EP06813086.3A
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German (de)
English (en)
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EP1960601B1 (fr
EP1960601A2 (fr
Inventor
Pavol Barla
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BASF Performance Products Ltd
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BASF Performance Products Ltd
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Classifications

    • 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
    • D21H17/20—Macromolecular organic compounds
    • 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
    • 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
    • D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/22—Agents rendering paper porous, absorbent or bulky
    • 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
    • D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
    • D21H23/76—Processes or apparatus for adding material to the pulp or to the paper characterised by choice of auxiliary compounds which are added separately from at least one other compound, e.g. to improve the incorporation of the latter or to obtain an enhanced combined effect

Definitions

  • the invention relates to a papermaking process for improving the absorption rate of especially tissue and fluff products.
  • the invention particularly relates to a papermaking process comprising applying at least one polymer and colloidal particles to a cellulosic fibre web.
  • Tissue paper and methods for making such paper are well known in the art.
  • Such paper is typically made by draining a cellulosic suspension and forming a web on a wire.
  • the cellulosic suspension is usually contained in the headbox before being deposited as a thin layer on a Fourdrinier wire to form a paper web.
  • the paper web is then typically dewatered by vacuum dewatering and further dewatered by pressing operations wherein the web is subjected to pressure developed by opposing mechanical members, for example cylindrical rolls or an extended nip press.
  • the dewatered web is then further pressed and dried by a steam drum apparatus known in the art as a Yankee cylinder.
  • Fluff pulp is typically made by forming a pulp sheet on a Fourdrinier wire which is subsequently pressed and dried to form bales or rolls.
  • the dry pulp is than defiberized using a hammer mill or a pin defiberizer to form fluff.
  • Typical products made from fluff are diapers and feminine hygiene products.
  • Fluff can also be used to produce air-laid paper products.
  • the absorption rate is one of the most essential properties for products made from tissue and fluff such as diapers, sanitary napkins, paper towels, facial and toilet tissues etc.
  • the rate of absorption is dependent both on the fibre surface chemistry and on the sheet structure.
  • WO 91/05108 describes a process for increasing the absorption rate of fluff pulp by increasing the specific surface area of the fibres. This is done by applying a porous layer of hydrophilic chemicals which are precipitated on the fibres.
  • JP 2003-251928 A relates to a method for coating and impregnating a paper sheet with a solution containing a water soluble polymer, colloidal silica and a sizing agent. It is an object of the invention to provide a process which increases the absorption rate of paper products, especially tissue and fluff products.
  • the present invention relates to a papermaking process in which tissue or fluff products are made by treating a cellulosic fibre web comprising applying to said cellulosic fibre web
  • natural and/or synthetic polymers can be used.
  • Suitable polymers can be cationic, anionic, amphoteric, or non-ionic in nature.
  • the polymer can have a molecular weight of from about 2,000 to about 500,000,000, for example from about 100,000 to about 100,000,000, or from about 200,000 to about 50,000,000.
  • the synthetic polymers can have a molecular weight of from about 2,000 to about 50,000,000, for example from about 100,000 to about 10,000,000, or from about 200,000 to about 1,000,000.
  • a cationic polymer is used.
  • suitable cationic polymers include cationic polysaccharides, e.g. starches, guar gums, cellulose derivatives, chitins, chitosans, glycans, galactans, glucans, xanthan gums, pectins, mannans, dextrins.
  • Suitable starches include potato, corn, wheat, tapioca, rice, waxy maize, and barley.
  • Cationic synthetic organic polymers such as cationic chain-growth polymers may also be used, e.g.
  • cationic vinyl addition polymers like acrylate-, acrylamide-, vinylamine-, vinylamido- and allylamine-based polymers, for example homo- and copolymers based on diallyldialkyl ammonium halide, e.g. diallyldimethyl ammonium chloride, as well as (meth)acrylamides and (meth)acrylates.
  • Further polymers include cationic step-growth polymers, e.g. cationic polyamidoamines, polyethylene imines, polyamines such as dimethylamine-epichlorhydrin copolymers; and polyurethanes.
  • suitable cationic organic polymers include those disclosed in WO 02/12626 . According to one embodiment, the cationic polymer is selected from the group consisting of a starch, guar gum, polydiallyldimethyl ammonium chloride, polyamidoamine, and mixtures thereof.
  • an anionic polymer is used.
  • anionic polymers induce anionic step-growth polymers, chain-growth polymers, polysaccharides, naturally occurring aromatic polymers and modifications thereof.
  • suitable anionic step-growth polymers include anionic benzene-based and naphthalene-based condensation polymers, preferably naphthalene-sulphonic acid based condensation polymers and naphthalene-sulphonate based condensation polymers; and addition polymers, i.e. polymers obtained by step-growth addition polymerisation, e.g. anionic polyurethane.
  • suitable anionic chain-gmwth polymers include anionic vinyl addition polymers, e.g.
  • acrylate- and acrylamide-based polymers comprising anionic or potentially anionic monomers like (meth)acrylic acid and polystyrenesulphonic acid.
  • suitable naturally occurring aromatic polymers and modifications thereof, i.e. modified naturally occurring aromatic anionic polymers include lignin-based polymers, preferably sulphonated lignins, e.g. lignosulphonates, kraft lignin, sulphonated kraft lignin, and tannin extracts.
  • lignin-based polymers preferably sulphonated lignins, e.g. lignosulphonates, kraft lignin, sulphonated kraft lignin, and tannin extracts.
  • Further examples of other suitable anionic organic polymers include those disposed in WO 02/12626 .
  • step-growth polymer refers to a polymer obtained by step-growth polymerization, also being referred to as step-reaction polymer and step-reaction polymerization, respectively.
  • chain-growth polymer refers to a polymer obtained by chain-growth polymerization, also being referred to as chain reaction polymer and chain reaction polymerization, respectively.
  • Colloidal particles that can be used include e.g. inorganic colloidal compounds of silica and metal oxides such as alumina, zirconia, magnesium oxide, titanium dioxide, iron oxide, zinc oxide; colloidal organic compounds, e.g. anionic or cationic cross-linked polyacrylamide; and combinations thereof.
  • the colloidal particles have an average particle diameter ranging from about 1 to about 1000, such as from about 2 to about 100, or from about 3 to about 40 nm.
  • the colloidal particles are colloidal silica particles.
  • the colloidal silica particles which also are referred to as silica sols, may be produced from e.g. precipitated silica, pyrogenic silica (fumed silica) or silica gels with sufficient purity, and mixtures thereof.
  • silica sols may be produced from e.g. precipitated silica, pyrogenic silica (fumed silica) or silica gels with sufficient purity, and mixtures thereof.
  • conventionally used sodium silicate may also be used.
  • Colloidal silica particles that can be used according to the invention may be modified and can contain other elements such as amines, aluminium and/or boron, which can be present in the particles and/or the continuous phase.
  • Boron-modified silica sols are described in e.g. US 2,630,410 .
  • the aluminium modified silica particles suitably have an Al 2 O 3 content of from about 0.05 to about 3 wt%, such as from about 0.1 to about 2 wt%.
  • the procedure of preparing an aluminium modified silica sol is further described in e.g. " The Chemistry of Silica", by Iler, K. Ralph, pages 407-409, John Wiley & Sons (1979 ) and in US 5 368 833 .
  • the colloidal silica particles are anionic colloidal silica particles.
  • the colloidal silica particles have an average particle diameter ranging from about 1 to about 100, such as from about 2 to about 50, or from about 3 to about 20 nm.
  • the colloidal silica particles have a specific surface area from 400 1300, suitably from about 400 to about 900 m 2 /g.
  • particle size refers to average size (diameter) of primary particles which may be aggregated or non-aggregated.
  • cationic colloidal particles are used.
  • a cationic polymer, an anionic polymer and cationic colloidal particles are applied in the mentioned order.
  • a cationic polymer is firstly applied whereafter anionic colloidal particles are applied.
  • cellulosic fibre web includes any sheet or web prepared from cellulosic fibres such as pulp sheets or paper webs.
  • the polymer and the colloidal particles can be applied to the pulp sheet prior to defiberization.
  • the polymer and the colloidal particles can be applied before or after drying of a cellulosic fibre web, e.g. during any stage in a converting machine for the production of a tissue product.
  • the cellulosic fibre web can have varying dry content when polymer and colloidal particles are applied.
  • the cellulosic fibre web has a dry content of from about 5 to about 95, such as from about 30 to about 60, or from about 30 to about 50 wt%.
  • the polymer can be applied by immersion of the cellulosic fibre web into a solution or dispersion of the polymer.
  • the colloidal particles can be applied by immersion of the cellulosic fibre web into a dispersion comprising the colloidal particles.
  • the polymer can be applied by spraying the polymer dispersion on the surface of the cellulosic fibre web.
  • Suitable polymer concentrations of the solution or dispersion depend on the viscosity of polymer solution or dispersion. The viscosity is dependent on inter alia the type and molecular weight of the polymer. However, suitable concentrations may be from about 0.001 to about 30, for example from about 0.01 to about 10, or from about 0.1 to about 5 wt%.
  • the polymer and the colloidal particles are applied by spraying.
  • the colloidal particles can be applied by spraying after the polymer has been applied.
  • the dispersion of colloidal particles can have a dry content of from about 0.001 to about 60, such as from about 0.05 to about 10, or from about 0.1 to about 5 wt%.
  • the polymer can be applied in an amount of from about 0.01 to about 35, such as from about 0.1 to about 15, or from about 0.5 to about 7 kg/ton dry cellulosic fibres.
  • the colloidal particles can be applied in an amount of from about 0.01 to about 35, such as from about 0.1 to about 15, or from about 0.5 to about 7 kg/ton dry cellulosic fibres.
  • the weight ratio of applied polymer to applied colloidal particles can be from about 1:50 to about 50:1, such as from about 1:5 to about 5:1, or from about 0.8:1 to about 1:0.8.
  • the polymer and the colloidal particles can be applied to the cellulosic fibre web.simultaneously, e.g. as a pre-blend or simultaneously at the same addition point in the process.
  • the polymer and the colloidal particles can be applied to the cellulosic fibre web separately.
  • the polymer is firstly applied to the cellulosic fibre web followed by application of the colloidal particles.
  • the surface of the cellulosic fibre web is usually negatively charged.
  • the surface of the fibres can be made cationically charged. This can be made by applying a cationic polymer prior to the addition of anionic colloidal particles.
  • a cationic polymer is applied on the web whereupon an anionic polymer subsequently is added prior to applying cationic colloidal particles.
  • Cellulosic fibre webs may include cellulosic fibres derived from wood pulp e.g. softwood and hardwood pulp including chemical pulp such as Kraft, sulphite and sulphate pulps, as well as mechanical pulps such as ground wood, thermomechanical pulp and chemical modified thermomechanical pulp (CTMP). Recycled fibres may also be used. Mixtures of chemical pulp and mechanical pulp may also be used.
  • tissue or fluff products other cellulosic fibres, such as rayon or cotton, can be comprised as well as synthetic fibres.
  • the tissue or fluff products can also comprise different superabsorbent materials.
  • additives may be added to the cellulosic suspension used to produce the cellulosic fibre web which in turn is processed to provide fluff or tissue products.
  • additives include e.g. wet strength agents, dry strength agents, wetting agents and debonding agents.
  • the stock was prepared according to the standard method SCAN-M2:64.
  • the sheet was cut into rectangular pieces (160x50mm) with the longer side parallel to the cross direction.
  • the test paper pieces were treated at ambient temperature by immersion in a polymer solution, referred to as a polyelectrolyte solution in the working examples herein (cationic, anionic or both solutions), and/or a silica sol dispersion.
  • An untreated reference sample was treated with tap water.
  • the concentrations of polyelectrolyte (polymer) and colloidal silica in the respective dispersions were 0.1 wt%.
  • the immersion time was 1 min in each of the dispersions.
  • the untreated sample (mentioned reference herein), a sample treated with only polymer, and a sample treated with only silica sol were couched in the same way.
  • the paper samples placed on a perforated stainless plate and were stretched by fixing their ends with paper tape or metallic strips and clips. The plates with the samples were placed in a drying box for drying (110°C/60 min). Prior to testing the absorption rate the samples were stored overnight in a conditioning room (23°C/ 50 %RH).
  • P1 Polydadmac Eka ATC 6140
  • P2 C-Starch PB 930
  • P3 Guar Gum Maypro-Bond
  • P4 Polyamideamine Kenores XO
  • A1 Silica sol BMA 0 (500m 2 /g)
  • A2 Silica sol Bindzil 50/80 (80m 2 /g)
  • A3 Silica sol HDK N20 (200m 2 /g)
  • A4 Silica sol NP590 (850m 2 /g)
  • the measurement of the water absorption rate was performed according to the standard method SCAN-P 62:88.
  • the absorption rate is determined in all three principal directions, i.e. the machine direction, the cross direction, and the direction perpendicular to the plane of the sheet.
  • the reported values are average values of three measurements.
  • Polymer P1 and colloidal particles A1 were used in example 2, which was performed as described in example 1. Measurements were performed on untreated paper (reference), paper treated with only polymer P1, as well as paper treated with both polymer P1 and colloidal particles A1. The absorption rate in mm/s was measured in the x, y and z directions. The results are given in table 1. Table 1 Direction x y z Reference 1.42 4.07 1.06 P1 0.74 1.86 0.38 P1+A1 4.95 10.71 8.27
  • Polymer P4 and colloidal particles A1 were used in example 3, which was performed as described in example 1. Measurements were performed on untreated paper (reference), paper treated with only polymer P4, paper treated with only colloidal particles A1, as well as paper treated with both polymer P4 and colloidal particles A1. The absorption rate in mm/s was measured in the x, y and z directions. The results are given in table 2. Table 2 Direction x y z Reference 1.23 3.25 0.89 P4 0.62 1.61 0.22 A1 1.71 4.48 1.4 P4+A1 3.27 6.3 3.4
  • Polymer P2 and colloidal particles A1 were used in example 4, which was performed as described in example 1. Measurements were performed on untreated paper (reference) and on paper treated with only polymer P2, paper treated with only colloidal particles A1, as well as paper treated with both polymer P2 and colloidal particles A1. The absorption rate in mm/s was measured in the x, y and z directions. The results are given in table 3. Table 3 Direction x y z Reference 1.48 3.83 1.18 P2 3.67 8.74 4.54 A1 1.81 4.57 1.43 P2+A1 5.66 11.48 9.08
  • Polymer P3 and colloidal particles A1 were used in example 5, which was performed as described in example 1. Measurements were performed on untreated paper (reference), on paper treated with only polymer P3, paper treated with only colloidal particles A1, as well as paper treated with both polymer P3 and colloidal particles A1. The absorption rate in mm/s was measured in the x, y and z directions. In trials 3 and 5, the samples were treated with polyelectrolyte and silica sol dispersion in accordance with example 1. In addition, after each immersion and couch stage, the samples were rinsed by immersion in deionized water for 1 min followed by couching. The results are given in table 4. Table 4 Direction Trial No.
  • Polymer P1 and colloidal particles A1-A4 were used in example 6, which was performed as described in example 1. Measurements were performed on untreated paper (reference) and on paper treated with only polymer P1, as well as paper treated with both polymer P1 and colloidal particles A1-A4. The absorption rate in mm/s was measured in the x, y and z directions. The results are given in table 5. Table 5 Direction x y z Reference 1.63 3.98 1.6 P1+A1 5.92 11.7 10.4 P1+A2 3.27 6.2 5.2 P1+A3 2.76 6.38 6.4 P1+A4 5.11 11.1 17.1

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  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Claims (13)

  1. Procédé de fabrication de papier dans lequel des produits en papier tissu ou duveteux sont réalisés en traitant une bande de fibre cellulosique comprenant l'application sur ladite bande de fibre cellulosique de :
    (i) au moins un polymère ; et
    (ii) des particules colloïdales, les particules colloïdales ayant une surface spécifique de 400 à 1300 m2/g.
  2. Procédé selon la revendication 1, dans lequel les particules colloïdales sont des particules de silice colloïdale.
  3. Procédé selon la revendication 1 ou 2, dans lequel les particules colloïdales sont anioniques.
  4. Procédé selon l'une quelconque des revendications 1 à 3, dans lequel les particules colloïdales ont une surface spécifique de 400 à 900 m2/g.
  5. Procédé selon l'une quelconque des revendications 1 à 4, dans lequel le polymère est cationique.
  6. Procédé selon l'une quelconque des revendications 1 à 5, dans lequel le polymère est choisi dans le groupe constitué de l'amidon, la gomme de guar, le chlorure de polydiallyldiméthylammonium, la polyamidoamine, et des mélanges de ceux-ci.
  7. Procédé selon l'une quelconque des revendications 1 à 6, dans lequel un polymère cationique, un polymère anionique et des particules colloïdales cationiques sont appliqués dans l'ordre mentionné.
  8. Procédé selon l'une quelconque des revendications 1 à 7, dans lequel le polymère est appliqué en une quantité de 0,01 à 35 kg/tonne de fibres cellulosiques sèches.
  9. Procédé selon l'une quelconque des revendications 1 à 8, dans lequel les particules colloïdales sont appliquées en une quantité de 0,01 à 35 kg/tonne de fibres cellulosiques sèches.
  10. Procédé selon l'une quelconque des revendications 1 à 9, dans lequel le rapport en poids du polymère aux particules colloïdales est dans la plage de 50:1 à 1:50.
  11. Procédé selon l'une quelconque des revendications 1 à 10, dans lequel le polymère et les particules colloïdales sont appliqués par pulvérisation.
  12. Procédé selon l'une quelconque des revendications 1 à 11, dans lequel le polymère et les particules colloïdales sont appliqués séparément.
  13. Procédé selon l'une quelconque des revendications 1 à 12, dans lequel le polymère et les particules colloïdales sont appliqués simultanément.
EP06813086.3A 2005-12-14 2006-11-10 Procede de fabrication de papier Not-in-force EP1960601B2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP06813086.3A EP1960601B2 (fr) 2005-12-14 2006-11-10 Procede de fabrication de papier

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP05112137 2005-12-14
PCT/SE2006/050466 WO2007069991A2 (fr) 2005-12-14 2006-11-10 Procede de fabrication de papier
EP06813086.3A EP1960601B2 (fr) 2005-12-14 2006-11-10 Procede de fabrication de papier

Publications (3)

Publication Number Publication Date
EP1960601A2 EP1960601A2 (fr) 2008-08-27
EP1960601B1 EP1960601B1 (fr) 2012-03-21
EP1960601B2 true EP1960601B2 (fr) 2015-05-06

Family

ID=36829795

Family Applications (1)

Application Number Title Priority Date Filing Date
EP06813086.3A Not-in-force EP1960601B2 (fr) 2005-12-14 2006-11-10 Procede de fabrication de papier

Country Status (5)

Country Link
EP (1) EP1960601B2 (fr)
AT (1) ATE550487T1 (fr)
ES (1) ES2383762T5 (fr)
PT (1) PT1960601E (fr)
WO (1) WO2007069991A2 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007140417A2 (fr) 2006-05-31 2007-12-06 Sequenom, Inc. Procédés et compositions destinés à l'extraction et l'amplification d'un acide nucléique à partir d'un échantillon
US7902345B2 (en) 2006-12-05 2011-03-08 Sequenom, Inc. Detection and quantification of biomolecules using mass spectrometry
US9404150B2 (en) 2007-08-29 2016-08-02 Sequenom, Inc. Methods and compositions for universal size-specific PCR
EP3514244B1 (fr) 2009-04-03 2021-07-07 Sequenom, Inc. Procédés de préparation d'acides nucléiques

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US3738957A (en) † 1971-03-18 1973-06-12 Du Pont Coacervates of polyvinyl alcohol and colloidal silica
EP0334400A1 (fr) † 1988-03-22 1989-09-27 Agfa-Gevaert N.V. Feuille ou bande portant une couche antistatique
EP0569285A2 (fr) † 1992-05-04 1993-11-10 Minnesota Mining And Manufacturing Company Colloides pour augmenter le coefficient de friction des revêtements sur blocs de papier sans carbone
WO2004099321A2 (fr) † 2003-05-02 2004-11-18 Hercules Incorporated Systemes aqueux contenant des premelanges d'additifs et procedes de preparation
WO2004106079A2 (fr) † 2003-05-28 2004-12-09 Clariant International Ltd Compositions de revetement, leur production et leur utilisation

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US2630410A (en) 1949-04-19 1953-03-03 Union Carbide & Carbon Corp Nongelling aqueous silica sols stabilized with boron compounds
SE8700058L (sv) * 1987-01-09 1988-07-10 Skogsindustriens Tekniska Fors Papperstillverkning
SE8701252D0 (sv) * 1987-03-03 1987-03-25 Eka Nobel Ab Sett vid framstellning av papper
US4992326A (en) * 1987-08-28 1991-02-12 Ncneil-Ppc, Inc. Hydrophilic polymers for incorporating deodorants in absorbent structures
SE500871C2 (sv) 1989-09-27 1994-09-19 Sca Research Ab Aluminiumsaltimpregnerade fibrer, sätt att framställa dessa, absorptionsmaterial för användning i hygienartiklar och användning av fibrerna som absorptionsmaterial
SE8903180D0 (sv) * 1989-09-27 1989-09-27 Sca Development Ab Saett att behandla fibrer av cellulosahaltigt material
SE500387C2 (sv) 1989-11-09 1994-06-13 Eka Nobel Ab Silikasoler, förfarande för framställning av silikasoler samt användning av solerna i pappersframställning
BR0112904A (pt) 2000-08-07 2003-07-01 Akzo Nobel Dispersão de engomagem
JP2003251928A (ja) * 2002-03-06 2003-09-09 Nippon Paper Industries Co Ltd インクジェット記録媒体

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3738957A (en) † 1971-03-18 1973-06-12 Du Pont Coacervates of polyvinyl alcohol and colloidal silica
EP0334400A1 (fr) † 1988-03-22 1989-09-27 Agfa-Gevaert N.V. Feuille ou bande portant une couche antistatique
EP0569285A2 (fr) † 1992-05-04 1993-11-10 Minnesota Mining And Manufacturing Company Colloides pour augmenter le coefficient de friction des revêtements sur blocs de papier sans carbone
WO2004099321A2 (fr) † 2003-05-02 2004-11-18 Hercules Incorporated Systemes aqueux contenant des premelanges d'additifs et procedes de preparation
WO2004106079A2 (fr) † 2003-05-28 2004-12-09 Clariant International Ltd Compositions de revetement, leur production et leur utilisation

Also Published As

Publication number Publication date
EP1960601B1 (fr) 2012-03-21
ES2383762T3 (es) 2012-06-26
ES2383762T5 (es) 2015-08-12
WO2007069991A2 (fr) 2007-06-21
PT1960601E (pt) 2012-06-25
WO2007069991A3 (fr) 2007-08-16
ATE550487T1 (de) 2012-04-15
EP1960601A2 (fr) 2008-08-27

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