WO1992007141A2 - Paper, paperboard and cardboard internal sizing process - Google Patents

Paper, paperboard and cardboard internal sizing process Download PDF

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Publication number
WO1992007141A2
WO1992007141A2 PCT/EP1991/001894 EP9101894W WO9207141A2 WO 1992007141 A2 WO1992007141 A2 WO 1992007141A2 EP 9101894 W EP9101894 W EP 9101894W WO 9207141 A2 WO9207141 A2 WO 9207141A2
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Prior art keywords
paper
cardboard
vinyl
resin glue
units
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PCT/EP1991/001894
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German (de)
French (fr)
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WO1992007141A3 (en
Inventor
Michael Kroener
Claudia Nilz
Norbert Sendhoff
Andreas Stange
Arnold De Clercq
Ulrich Riebeling
Original Assignee
Basf Aktiengesellschaft
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Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft
Priority to DE59104096T priority Critical patent/DE59104096D1/en
Priority to CA002085348A priority patent/CA2085348C/en
Priority to JP51621891A priority patent/JP3176620B2/en
Priority to EP91917563A priority patent/EP0553135B1/en
Publication of WO1992007141A2 publication Critical patent/WO1992007141A2/en
Publication of WO1992007141A3 publication Critical patent/WO1992007141A3/en
Priority to FI931642A priority patent/FI97405C/en

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    • 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • D21H17/45Nitrogen-containing groups
    • 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
    • D21H21/00Non-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
    • D21H21/14Non-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
    • D21H21/16Sizing or water-repelling agents

Definitions

  • the invention relates to a process for the mass sizing of paper, cardboard and cardboard using resin glue and cationic polymers which contain vinylamine units in copolymerized form as a fixing agent.
  • N-vinylformamide Partially hydrolyzed homopolymers of N-vinylformamide are known from US Pat. No. 4,421,602, which contain N-vinylformamide and vinylamine units. They are used as retention, drainage and flocculants in the manufacture of paper.
  • hydrophobic, cellulose-reactive sizing agents and fixing and sizing accelerating agents made of polymers which contain primary, secondary or tertiary amino and / or quaternary ammonium groups directly or bound via side chains.
  • cationic polymers also include hydrolyzed polymers of N-vinylformamide and partially hydrolyzed copolymers of N-vinyl acetamide and vinyl acetate.
  • hydrophobic, cellulose-reactive sizing agents are preferably alkyl ketene dimers, anhydrides, such as rosin anhydride and isocyanates.
  • the best-known bulk glue based on natural products is resin glue. These are compounds which are non-reactive with the cellulose fiber and which are deposited on the cellulose fibers in the paper stock with the addition of fixing agents. As
  • Fixing agents come for example aluminum sulfate or according to the
  • the present invention is based on the object of demonstrating a process for mass sizing paper, cardboard and cardboard with resin glue, in which the sizing can be carried out in the neutral pH range and in which aging-resistant papers are obtained.
  • resin glue is understood to mean the products based on natural materials that are usually used for the mass sizing of paper, e.g. Resin glue from hydrogenated rosin, tall resin glue, reinforced resin glue, dry resin glue or free resin-rich emulsions. These products are non-reactive resin glues which, when used alone in the bulk of paper, practically do not glue, but always have to be used together with a fixing agent.
  • resin glues are described, for example, in the magazine “Papier”, volume 43 (5), 188-192 (1989). As with known processes for the mass sizing of paper, resin glue is also used in the present process in an amount of approximately 1 to 4, preferably 1.5 to 3% by weight, based in each case on dry paper stock.
  • the paper is sized by mass in the presence of small amounts of aluminum sulfate and / or alum using cationic polymers which contain vinylamine units in copolymerized form.
  • Aluminum sulfate and alum are used in amounts of ⁇ 5% by weight, preferably 2 to 3% by weight, as a precipitant for resin glue.
  • the cationic polymers surprisingly act as fixatives for non-reactive resin glue.
  • Polymers of this type are known, for example, from the references cited in the prior art US Pat. No. 4,421,602 and EP-A-0 216 387. They are produced by hydrolysis of homopolymers and copolymers containing N-vinylamides in copolymerized form.
  • Such polymers contain the following characteristic structures: (I),
  • R, R 1 H, C 1 - to C 6 alkyl.
  • N-vinylformamide, N-vinyl acetamide, N-vinyl-N-methylformamide, N-vinylpropionamide or N-vinylbutyramide are polymerized.
  • the structure is obtained by hydrolysis using acids, for example hydrochloric acid, sulfuric acid, phosphoric acid or under the action of bases, such as sodium hydroxide solution or potassium hydroxide solution, with the grouping -CO-R 1 being split off: (II),
  • the hydrolysis can be 0.1 to 100%.
  • the preferred polymers containing copolymerized vinylamine units include compounds which are obtained by copolymerizing
  • Degree of hydrolysis of the polymerized N-vinylformamide units is 0.1 to 100%, preferably at least 10%.
  • Such copolymers are described in EP-A-0216387.
  • the monomer of component (a) can be e.g. Use N-vinyl-N-methylformamide, N-vinylacetamide, N-vinyl-N-methylacetamide, N-vinylpropionamide or N-vinylbutyramide.
  • the copolymerized monomer units (b) can also be hydrolyzed, so that in the case of the latter comonomers, the copolymers are then additionally, e.g. Polymerized vinyl alcohol units included.
  • the hydrolysis of the acetyl and / or propionyl groups from the copolymerized units (b) of the copolymers can be 0.1 to 100%.
  • the homopolymers and copolymers containing copolymerized vinylamine units have K values of 5 to 300, preferably 15 to 150.
  • Polyvinylamines and hydrolyzed copolymers of N-vinylformamide with K values of 20 to 115 are particularly preferred.
  • the cationic polymers containing copolymerized vinylamine units are water-soluble. They are added directly to the paper stock for mass sizing or can also be added to the paper stock in the form of a mixture with the resin glue. In the case of a separate dosage of polymer and resin glue, it does not matter whether the resin glue is added to the paper pulp first or the cationic polymer, white oil
  • Paper pulp always has sufficient mixing of the components. Based on 100 parts by weight of resin glue, 1 to 100, preferably 5 to 30 parts by weight of at least one cationic polymer which contains vinylamine units in copolymerized form are used.
  • wood pulp includes wood pulp, thermomechanical material
  • TMP chemo-thermomechanical material
  • CMP chemo-thermomechanical material
  • RMP refiner mechanical pulp
  • pulp For example, sulfate, sulfite and sodium pulps come into consideration.
  • the unbleached pulps which are also referred to as unbleached kraft pulp, are preferably used.
  • Suitable annual plants for the production of paper materials are, for example, rice,
  • Waste paper is also used to produce the pulps, either alone or in a mixture with other fibrous materials.
  • the pulps are mixed with resin glue and at least one polymer to be used according to the invention as a fixing agent and dewatered in a known manner on a sieve of a paper machine.
  • the pulp concentration is 0.1 to 1.5% by weight, the pulp pH up to 8. Preference is given to
  • Pulps with pH values from 6 to 7.5 Pulps with pH values from 6 to 7.5.
  • the parts given in the examples are parts by weight. The percentages relate to the weight of the fabrics.
  • the K values were according to H. Fikentscher, Cellulose-Chemie, Vol. 18, 48-64 and 71-74 (1932) in
  • the preparation uptake is calculated from the weight gain as follows:
  • 50% low-viscosity resin soap made from chemically reinforced
  • Natural resins with a total resin acid number of 170, a free resin content of approx. 2% and a Brookfield viscosity at 20 ° C and 20 rpm of 1000 mPas.
  • a paper fabric is made from 100% bleached birch sulfate pulp with the addition of 40% chalk.
  • the degree of grinding is 35 ° SR (Schopper-Riegler). Based on the solids content, 1.5% by weight of the sizing agent, 3% by weight of alum and then to this substance are added
  • Sheets were each dried on a steam-heated drying cylinder at 90 ° C to a residual moisture of 6 to 10%.
  • Example 1 was repeated with the only exception that instead of 0.1% by weight of fixative 1, only 3% by weight of alum was used as fixative and precipitant.
  • the pH of the pulp was 7.
  • Table 1 Immediate sizing

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paper (AREA)
  • Sanitary Thin Papers (AREA)
  • Machines For Manufacturing Corrugated Board In Mechanical Paper-Making Processes (AREA)

Abstract

According to a paper, paperboard and cardboard internal sizing process, resi n size is used, as well as cationic polymers containing polymerized vinylamine units as fixing agents for the resin size.

Description

Verfahren zur Masseleimung von Papier, Pappe und Karton  Process for mass sizing paper, cardboard and cardboard
Beschreibung Die Erfindung betrifft ein Verfahren zur Masseleimung von Papier, Pappe und Karton unter Verwendung von Harzleim und kationischen Polymerisaten, die Vinylamineinheiten einpolymerisiert enthalten, als Fixiermittel. The invention relates to a process for the mass sizing of paper, cardboard and cardboard using resin glue and cationic polymers which contain vinylamine units in copolymerized form as a fixing agent.
Aus der US-PS 4421 602 sind partiell hydrolysierte Homopolymerisate des N-Vinylformamids bekannt, die N-Vinylformamid- und Vinylamineinheiten enthalten. Sie werden als Retentions-, Entwässerungs- und Flockungsmittel bei der Herstellung von Papier verwendet. Partially hydrolyzed homopolymers of N-vinylformamide are known from US Pat. No. 4,421,602, which contain N-vinylformamide and vinylamine units. They are used as retention, drainage and flocculants in the manufacture of paper.
Aus der EP-A-0 216 387 ist bekannt, daß man Copolymerisate aus 95 bis 10 mol-% N-Vinylformamid und 5 bis 90 mol-% eines ethylenisch ungesättigten Monomeren aus der Gruppe Vinylacetat, Vinylpropionat, der C1- bis C4-Alkylvinylether, N-Vinylpyrrolidon, der Ester, Nitriie und Amide von Acrylsäure und Methacrylsäure in zumindest partiell hydrolysierter Form, bei der bis zu 100 mol-% der Formylgruppen aus dem Copolymerisat abgespalten sind, in Mengen von 0,1 bis 5 Gew.-%, bezogen auf trockene Fasern, dem Papierstoff vor der Blattbildung als Naß- und Trockenverfestigungsmittel für Papier zusetzt. From EP-A-0 216 387 it is known that copolymers of 95 to 10 mol% of N-vinylformamide and 5 to 90 mol% of an ethylenically unsaturated monomer from the group vinyl acetate, vinyl propionate, the C 1 - to C 4 -Alkylvinylether, N-vinylpyrrolidone, the esters, nitrites and amides of acrylic acid and methacrylic acid in at least partially hydrolyzed form, in which up to 100 mol% of the formyl groups are split off from the copolymer, in amounts of 0.1 to 5% by weight. %, based on dry fibers, the paper stock before sheet formation as a wet and dry strength agent for paper.
Aus der DE-OS 3203 189 sind Leimungsmittel auf Basis hydrophober, cellulosereaktiver Leimungsstoffe und Fixier- und Leimungsbeschleunigungs- mitteln aus Polymeren bekannt, die primäre, sekundäre oder tertiäre Amino- und/oder quartäre Ammoniumgruppen direkt oder über Seitenketten gebunden enthalten. Zu diesen kationischen Polymerisaten gehören auch hydrolysierte Polymerisate des N-Vinylformamids und partiell hydrolysierte Copolymerisäte aus N-Vinylacetamid und Vinylacetat. Gemäß den Angaben in der OE-OS sind hydrophobe, cellulosereaktive Leimungsstoffe vorzugsweise Alkylketendimere, Anhydride, wie Kolophoniumanhydrid und Isocyanate. From DE-OS 3203 189 sizing agents based on hydrophobic, cellulose-reactive sizing agents and fixing and sizing accelerating agents made of polymers are known which contain primary, secondary or tertiary amino and / or quaternary ammonium groups directly or bound via side chains. These cationic polymers also include hydrolyzed polymers of N-vinylformamide and partially hydrolyzed copolymers of N-vinyl acetamide and vinyl acetate. According to the information in the OE-OS, hydrophobic, cellulose-reactive sizing agents are preferably alkyl ketene dimers, anhydrides, such as rosin anhydride and isocyanates.
Das bekannteste Masseleimungsmittel auf Basis von Naturprodukten ist der Harzleim. Hierbei handelt es sich um Verbindungen, die gegenüber der Cellulosefaser nicht-reaktiv sind und die unter Zusatz von Fixiermitteln auf den Cellulosefasern im Papierstoff niedergeschlagen werden. Als The best-known bulk glue based on natural products is resin glue. These are compounds which are non-reactive with the cellulose fiber and which are deposited on the cellulose fibers in the paper stock with the addition of fixing agents. As
Fixiermittel kommen beispielsweise Aluminiumsulfat oder gemäß der Fixing agents come for example aluminum sulfate or according to the
DE-AS 10 70 916 und der EP-PS 0 187666 kationische Dicyandiamidharze in Betracht. Während die Wirksamkeit der kationischen Dicyandiamidharze noch verbesserungsbedürftig ist, haben Aluminiumsulfat und Alaun den Nachteil, daß in ihrer Gegenwart nicht mit Calciumcarbonat als Füllstoff gearbeitet werden kann und daß die so erhältlichen Papiere wegen des Arbeitens im sauren pH-Bereich nicht ausreichend alterungsbeständig sind. DE-AS 10 70 916 and EP-PS 0 187666 cationic dicyandiamide resins into consideration. While the effectiveness of the cationic dicyandiamide resins is still in need of improvement, aluminum sulfate and alum have the disadvantage that they do not work with calcium carbonate as a filler in their presence can and that the papers available in this way are not sufficiently resistant to aging because of working in the acidic pH range.
Der vorliegenden Erfindung liegt die Aufgabe zugrunde, ein Verfahren zur Masseleimung von Papier, Pappe und Karton mit Harzleim aufzuzeigen, bei dem die Leimung im neutralen pH-Bereich durchführbar ist und bei dem man alterungsbeständige Papiere erhält. The present invention is based on the object of demonstrating a process for mass sizing paper, cardboard and cardboard with resin glue, in which the sizing can be carried out in the neutral pH range and in which aging-resistant papers are obtained.
Die Aufgabe wird erfindungsgemäß gelöst mit einem Verfahren zur Masseleimung von Papier, Pappe und Karton unter Verwendung von Harzleim und eines Fixiermittels zum Fixieren des Harzleims auf den Cellulosefasern, wenn man als Fixiermittel kationische Polymerisate einsetzt, die Vinylamineinheiten einpolymerisiert enthalten. Unter Harzleim werden im vorliegenden Zusammenhang die üblicherweise zur Masseleimung von Papier verwendeten Produkte auf Basis von Naturstoffen verstanden, z.B. Harzleime aus hydriertem Kolophonium, Tallharzleime, verstärkte Harzleime, Trockenharzleime oder freiharzreiche Emulsionen. Bei diesen Produkten handelt es sich um nicht-reaktive Harzleime, die bei alleiniger Anwendung in der Masse Papier praktisch nicht leimen, sondern immer zusammen mit einem Fixiermittel eingesetzt werden müssen. Geeignete Harzleime sind beispielsweise in der Zeitschrift "Papier", Band 43 (5), 188-192 (1989) beschrieben. Wie bei bekannten Verfahren zur Masseleimung von Papier wird auch beim vorliegenden Verfahren Harzleim in einer Menge von ca. 1 bis 4, vorzugsweise 1,5 bis 3 Gew.-%, jeweils bezogen auf trockenen Papierstoff angewendet. The object is achieved according to the invention with a process for the mass sizing of paper, cardboard and cardboard using resin glue and a fixing agent for fixing the resin glue on the cellulose fibers if cationic polymers are used as the fixing agent which contain copolymerized vinylamine units. In the present context, resin glue is understood to mean the products based on natural materials that are usually used for the mass sizing of paper, e.g. Resin glue from hydrogenated rosin, tall resin glue, reinforced resin glue, dry resin glue or free resin-rich emulsions. These products are non-reactive resin glues which, when used alone in the bulk of paper, practically do not glue, but always have to be used together with a fixing agent. Suitable resin glues are described, for example, in the magazine "Papier", volume 43 (5), 188-192 (1989). As with known processes for the mass sizing of paper, resin glue is also used in the present process in an amount of approximately 1 to 4, preferably 1.5 to 3% by weight, based in each case on dry paper stock.
Erfindungsgemäß erfolgt die Masseleimung von Papier in Anwesenheit von geringen Mengen Aluminiumsulfat und/oder Alaun unter Verwendung von kationischen Polymerisaten, die Vinylamineinheiten einpolymerisiert enthalten. Aluminiumsulfat und Alaun werden in Mengen < 5 Gew.-%, vorzugsweise 2 bis 3 Gew.-% als Fällungsmittel für Harzleim verwendet. Die kationischen Polymerisate wirken überraschenderweise als Fixiermittel für nicht-reaktiven Harzleim. Polymerisate dieser Art sind beispielsweise aus den zum Stand der Technik genannten Literaturstellen US-PS 4421 602 und der EP-A-0 216 387 bekannt. Sie werden durch Hydrolyse von N-Vinylamide einpolymerisiert enthaltenden Homo- und Copolymerisäten hergestellt. Solche Polymerisate enthalten folgende charakteristische Strukturen: (I),
Figure imgf000005_0001
According to the invention, the paper is sized by mass in the presence of small amounts of aluminum sulfate and / or alum using cationic polymers which contain vinylamine units in copolymerized form. Aluminum sulfate and alum are used in amounts of <5% by weight, preferably 2 to 3% by weight, as a precipitant for resin glue. The cationic polymers surprisingly act as fixatives for non-reactive resin glue. Polymers of this type are known, for example, from the references cited in the prior art US Pat. No. 4,421,602 and EP-A-0 216 387. They are produced by hydrolysis of homopolymers and copolymers containing N-vinylamides in copolymerized form. Such polymers contain the following characteristic structures: (I),
Figure imgf000005_0001
in der R, R1 = H, C1- bis C6-Alkyl bedeuten. Zur Herstellung von Verbindungen, die ausschließlich Struktureinheiten der Formel I enthalten, polymerisiert man z.B. N-Vinylformamid, N-Vinylacet- amid, N-Vinyl-N-methylformamid, N-Vinylpropionamid oder N-Vinylbutyramid. Aus den Verbindungen mit Strukturelementen der Formel I entsteht durch Hydrolyse unter Verwendung von Säuren, z.B. Salzsäure, Schwefelsäure, Phosphorsäure oder unter Einwirkung von Basen, wie Natronlauge oder Kalilauge, unter Abspaltung der Gruppierung -CO-R1 die Struktur: (II),in which R, R 1 = H, C 1 - to C 6 alkyl. For the preparation of compounds which contain only structural units of the formula I, for example, N-vinylformamide, N-vinyl acetamide, N-vinyl-N-methylformamide, N-vinylpropionamide or N-vinylbutyramide are polymerized. From the compounds with structural elements of the formula I, the structure is obtained by hydrolysis using acids, for example hydrochloric acid, sulfuric acid, phosphoric acid or under the action of bases, such as sodium hydroxide solution or potassium hydroxide solution, with the grouping -CO-R 1 being split off: (II),
Figure imgf000005_0002
Figure imgf000005_0002
in der R = H, C1- bis C6-Alkyl bedeutet. Bei einer 100 %igen Hydrolyse sämtlicher Einheiten der Struktur I im Polymerisat erhält man Polyvinylamine. Sofern nur eine partielle Hydrolyse durchgeführt wird, enthalten die aus den N-Vinylamiden hergestellten Polymerisate Einheiten der Strukturen I und II. Vorzugsweise wird als N-Vinyl- amid die Verbindung der Formel (III),in which R = H, C 1 - to C 6 alkyl. A 100% hydrolysis of all units of structure I in the polymer gives polyvinylamines. If only partial hydrolysis is carried out, the polymers prepared from the N-vinylamides contain units of structures I and II. The compound of the formula (III)
Figure imgf000005_0003
Figure imgf000005_0003
eingesetzt, d.h. N-Vinylformamid. Partiell hydrolysierte Homopolymerisate der Verbindung III sind aus der obengenannten US-PS 4421 602 bekannt. Die Hydrolyse kann 0,1 bis 100 % betragen. Zu den bevorzugt in Betracht kommenden, Vinylamineinheiten einpolymerisiert enthaltenden Polymerisaten gehören Verbindungen, die durch Copolymerisieren von used, i.e. N-vinyl formamide. Partially hydrolyzed homopolymers of the compound III are known from the above-mentioned US Pat. No. 4,421,602. The hydrolysis can be 0.1 to 100%. The preferred polymers containing copolymerized vinylamine units include compounds which are obtained by copolymerizing
(a) 1 bis 99, vorzugsweise 10 bis 90 mol-% N-Vinylformamid und (a) 1 to 99, preferably 10 to 90 mol% of N-vinylformamide and
(b) 99 bis 1 mol-% monoethylenisch ungesättigten Monomeren aus der Gruppe Vinylacetat, vinylpropionat, der C1- bis C4-Alkylvinylether, N-Vinyl- pyrrolidon, der Ester, Nitrile, Amide, N-Alkylamide und Sulfogruppen tragenden N-Alkylamide der Acrylsäure und Methacrylsäure und (b) 99 to 1 mol% of monoethylenically unsaturated monomers from the group vinyl acetate, vinyl propionate, the C 1 to C 4 alkyl vinyl ether, N-vinyl pyrrolidone, the esters, nitriles, amides, N-alkylamides and sulfo groups-bearing N-alkylamides of acrylic acid and methacrylic acid and
Mischungen dieser Monomeren und anschließende Hydrolyse der Amidgruppen der Struktureinheiten I der Mixtures of these monomers and subsequent hydrolysis of the amide groups of structural units I
Polymerisate in Aminogruppen der Struktur II erhältlich sind. Der Polymers in amino groups of structure II are available. The
Hydrolysegrad der einpolymerisierten N-Vinylformamideinheiten beträgt 0,1 bis 100 %, vorzugsweise mindestens 10 %. Solche Copolymerisate werden in der EP-A-0216387 beschrieben. Außer N-vinylformamid kann man als Monomer der Komponente (a) z.B. N-Vinyl-N- methylformamid, N-Vinylacetamid, N-Vinyl-N-methylacetamid, N-Vinylpropionamid oder N-Vinylbutyramid einsetzen. Bei der Hydrolyse von Copolymerisaten aus N-Vinylformamid und Vinylacetat oder Vinylpropionat können, je nach Reaktionsbedingungen, auch noch die einpolymerisierten Moπomereinheiten (b) hydrolysiert werden, so daß die Copolymerisate dann im Fall der zuletztgenannten Comonomeren zusätzlich, z.B. Vinylalkohol-Einheiten einpolymerisiert enthalten. Die Hydrolyse der Acetyl- und/oder Propionyl- gruppen aus den einpolymerisierten Einheiten (b) der Copolymerisate kann 0,1 bis 100 % betragen.  Degree of hydrolysis of the polymerized N-vinylformamide units is 0.1 to 100%, preferably at least 10%. Such copolymers are described in EP-A-0216387. In addition to N-vinylformamide, the monomer of component (a) can be e.g. Use N-vinyl-N-methylformamide, N-vinylacetamide, N-vinyl-N-methylacetamide, N-vinylpropionamide or N-vinylbutyramide. In the hydrolysis of copolymers of N-vinylformamide and vinyl acetate or vinyl propionate, depending on the reaction conditions, the copolymerized monomer units (b) can also be hydrolyzed, so that in the case of the latter comonomers, the copolymers are then additionally, e.g. Polymerized vinyl alcohol units included. The hydrolysis of the acetyl and / or propionyl groups from the copolymerized units (b) of the copolymers can be 0.1 to 100%.
Die Vinylamineinheiten einpolymerisiert enthaltenden Homo- und Copolymerisate haben K-Werte von 5 bis 300, vorzugsweise 15 bis 150. Besonders bevorzugt sind Polyvinylamine und hydrolysierte Copolymerisate des N-Vinyl- formamids mit K-Werten von 20 bis 115. The homopolymers and copolymers containing copolymerized vinylamine units have K values of 5 to 300, preferably 15 to 150. Polyvinylamines and hydrolyzed copolymers of N-vinylformamide with K values of 20 to 115 are particularly preferred.
Die kationischen, Vinylamineinheiten einpolymerisiert enthaltenden Polymerisate sind wasserlöslich. Sie werden zur Masseleimung dem Papierstoff direkt zugesetzt oder können auch in Form einer Mischung mit dem Harzleim dem Papierstoff zugefügt werden. Im Fall einer getrennten Dosierung von Polymerisat und Harzleim ist es gleichgültig, ob der Harzleim zuerst zum Papierstoff zugefügt wird oder das kationische Polymerisat, wei l im The cationic polymers containing copolymerized vinylamine units are water-soluble. They are added directly to the paper stock for mass sizing or can also be added to the paper stock in the form of a mixture with the resin glue. In the case of a separate dosage of polymer and resin glue, it does not matter whether the resin glue is added to the paper pulp first or the cationic polymer, white oil
Papierstoff immer eine ausreichende Durchmischung der Komponenten stattfindet. Bezogen auf 100 Gew.-Teile Harzleim verwendet man 1 bis 100, vorzugsweise 5 bis 30 Gew.-Teile mindestens eines kationischen Polymerisats, das Vinylamineinheiten einpolymerisiert enthält. Paper pulp always has sufficient mixing of the components. Based on 100 parts by weight of resin glue, 1 to 100, preferably 5 to 30 parts by weight of at least one cationic polymer which contains vinylamine units in copolymerized form are used.
Als Faserstoffe zur Herstellung der Pulpen kommen sämtliche dafür gebräuchlichen Qualitäten in Betracht, z.B. Holzstoff, gebleichter und ungebleichter Zellstoff sowie Papierstoffe aus allen Einjahrespflanzen. ZuAs fiber materials for the production of the pulps, all the qualities commonly used for this purpose come into consideration, e.g. Wood pulp, bleached and unbleached pulp and paper pulp from all annual plants. To
Holzstoff gehören beispielsweise Holzschliff, thermomechanischer StoffFor example, wood pulp includes wood pulp, thermomechanical material
(TMP), chemo-thermomechanischer Stoff (CTMP), Druckschliff, Halbzellstoff, Hochausbeute-Zellstoff und Refiner Mechanical Pulp (RMP). Als Zellstoffe kommen beispielsweise Sulfat-, Sulfit- und Natronzellstoffe in Betracht. (TMP), chemo-thermomechanical material (CTMP), pressure grinding, semi-pulp, high-yield pulp and refiner mechanical pulp (RMP). As pulp For example, sulfate, sulfite and sodium pulps come into consideration.
Vorzugsweise verwendet man die ungebleichten Zellstoffe, die auch als ungebleichter Kraftzellstoff bezeichnet werden. Geeignete Einjahres- pflanzen zur Herstellung von Papierstoffen sind beispielsweise Reis,  The unbleached pulps, which are also referred to as unbleached kraft pulp, are preferably used. Suitable annual plants for the production of paper materials are, for example, rice,
Weizen, Zuckerrohr und Kenaf. Zur Herstellung der Pulpen wird auch Altpapier verwendet, entweder allein oder in Mischung mit anderen Faserstoffen. Die Pulpen werden zur Herstellung von Papier, Pappe und Karton mit Harzleim und mindestens einem erfindungsgemäß zu verwendenden Polymerisat als Fixiermittel gemischt und in bekannter Weise auf einem Sieb einer Papiermaschine entwässert. Die Stoffkonzentration der Pulpen beträgt 0,1 bis 1,5 Gew.-%, der pH-Wert der Pulpen bis zu 8. Bevorzugt werden Wheat, sugar cane and kenaf. Waste paper is also used to produce the pulps, either alone or in a mixture with other fibrous materials. To produce paper, cardboard and cardboard, the pulps are mixed with resin glue and at least one polymer to be used according to the invention as a fixing agent and dewatered in a known manner on a sieve of a paper machine. The pulp concentration is 0.1 to 1.5% by weight, the pulp pH up to 8. Preference is given to
Pulpen mit pH-Werten von 6 bis 7,5. Pulps with pH values from 6 to 7.5.
Die in den Beispielen angegebenen Teile sind Gewichtsteile. Die Angaben in Prozent beziehen sich auf das Gewicht der Stoffe. Die K-Werte wurden nach H. Fikentscher, Cellulose-Chemie, Band 18, 48-64 und 71-74 (1932) in The parts given in the examples are parts by weight. The percentages relate to the weight of the fabrics. The K values were according to H. Fikentscher, Cellulose-Chemie, Vol. 18, 48-64 and 71-74 (1932) in
5 %iger wäßriger Kochsalzlösung bei einer Temperatur von 25°C und einer 5% aqueous saline solution at a temperature of 25 ° C and one
Polymerkonzentration von 1 Gew.-% bestimmt. Die Leimungsgüte wurde mit Polymer concentration of 1 wt .-% determined. The sizing quality was included
Hilfe des Cobb-Wertes nach DIN 53 132 und der Tintenschwimmdauer bis zum 50 %igen Durchschlag ermittelt. Zur Charakterisierung der Leimung wurde außerdem die Präparationsaufnahme bestimmt. Dazu wird ein Papierstreifen (80 cm x 10 cm) durch eine Laborleimpresse mit konstant eingestelltem Using the Cobb value according to DIN 53 132 and the ink floating time up to 50% breakthrough. The preparation image was also determined to characterize the sizing. For this, a paper strip (80 cm x 10 cm) is passed through a laboratory size press with a constant set
Anpreßdruck und einer Geschwindigkeit von 10 m/min gezogen. Als Testflüssigkeit wird Trinkwasser eingesetzt. Aus der Gewichtszunahme wird die Präparationsaufnahme folgendermaßen berechnet: Contact pressure and a speed of 10 m / min. Drinking water is used as the test liquid. The preparation uptake is calculated from the weight gain as follows:
(Gewicht nach Leimpresse - Gewicht vor Leimpresse) x 100(Weight after size press - weight before size press) x 100
Präparationsaufnahme =_________________________________________________________________ Preparation admission = _________________________________________________________________
Gewicht des getrockneten Musters (atro)  Weight of the dried sample (atro)
Folgende Einsatzstoffe wurden verwendet: The following ingredients were used:
Leimungsmittel 1 Sizing agent 1
50 %ige niedrigviskose Harzseife, hergestellt aus chemisch verstärkten  50% low-viscosity resin soap, made from chemically reinforced
Naturharzen mit einer Gesamtharzsäurezahl von 170, einem Freiharzgehalt von ca. 2 % und einer Viskosität nach Brookfield bei 20°C und 20 UpM von 1000 mPas. Natural resins with a total resin acid number of 170, a free resin content of approx. 2% and a Brookfield viscosity at 20 ° C and 20 rpm of 1000 mPas.
Fixiermittel 1 Fixing agent 1
11 %ige wäßrige Lösung eines Copolymerisats, das 98 % Vinylamineinheiten und 2 % N-Vinylformamideinheiten enthielt und einen K-Wert von 87 hatte. 11% aqueous solution of a copolymer which contained 98% vinylamine units and 2% N-vinylformamide units and had a K value of 87.
Der pH-Wert der wäßrigen Lösung betrug 3,5. Fixiermittel 2 The pH of the aqueous solution was 3.5. Fixing agent 2
12 %ige wäßrige Lösung (pH-Wert 3,5) eines Copolymerisats, das 68 % vinyl- amin-, 2 % N-Vinylformamid-, 25 % Vinylalkohol- und 5 % Vinylacetat- Einheiten enthielt und einen K-Wert von 105 hatte. 12% aqueous solution (pH 3.5) of a copolymer which contained 68% vinylamine, 2% N-vinylformamide, 25% vinyl alcohol and 5% vinyl acetate units and had a K value of 105 .
Fixiermittel 3 Fixing agent 3
17 %ige wäßrige Lösung eines Copolymerisats, das 45 % Vinylamin- und 55 % N-Vinylformamid-Einheiten enthielt und einen K-Wert von 87 hat. Der pH-Wert der wäßrigen Lösung betrug 3,5. 17% aqueous solution of a copolymer which contained 45% vinylamine and 55% N-vinylformamide units and has a K value of 87. The pH of the aqueous solution was 3.5.
Beispiele Man stellt einen Papierstoff aus 100 % gebleichtem Birkensulfatzellstoff unter Zusatz von 40 % Kreide her. Der Mahlgrad beträgt 35°SR (Schopper- Riegler). Zu diesem Stoff gibt man, bezogen auf den Feststoffgehalt, 1,5 Gew.-% des Leimungsmittels, 3 Gew.-% Alaun und anschließend Examples A paper fabric is made from 100% bleached birch sulfate pulp with the addition of 40% chalk. The degree of grinding is 35 ° SR (Schopper-Riegler). Based on the solids content, 1.5% by weight of the sizing agent, 3% by weight of alum and then to this substance are added
0,1 Gew.-%, bezogen auf Feststoff, eines der in Tabellen 1 und 2 genannten Fixiermittel. Der pH-Wert des Stoffes bleibt dabei unverändert auf pH 7 eingestellt. Bei allen Beispielen fügte man zum Papierstoff zusätzlich noch 0,3 % eines handelsüblichen schwach-kationischen Polyacrylamids vom K-Wert 130 als Retentionsmittel zu und bildete danach auf einem Rapid- Köthen-Blattbildner Blätter eines Flächengewichts von 100 g/m2. Die 0.1% by weight, based on solids, of one of the fixing agents mentioned in Tables 1 and 2. The pH of the substance remains unchanged at pH 7. In all examples, 0.3% of a commercially available weakly cationic polyacrylamide with a K value of 130 was added to the paper stock as a retention agent, and sheets with a basis weight of 100 g / m 2 were then formed on a Rapid-Köthen sheet former. The
Blätter wurden jeweils auf einem mit Dampf beheizten Trockenzylinder bei 90°C bis zu einer Restfeuchte von 6 bis 10 % getrocknet. Sheets were each dried on a steam-heated drying cylinder at 90 ° C to a residual moisture of 6 to 10%.
Bei allen Beispielen wurde unmittelbar nach dem Trocknen die Präparationsaufnahme, der Cobb-Wert und die Tintenschwimmzeit bestimmt. Diese Ergebnisse sind in Tabelle 1 zusammengestellt. Die Blätter wurden dann einen Tag bei 23°C und einer relativen Luftfeuchte von 50 % gelagert. Danach bestimmte man die Präparationsaufnähme, den Cobb-Wert und die Tintenschwimmzeit. Die dabei erhaltenen Meßergebnisse sind in Tabelle 2 angegeben. In all examples, the preparation uptake, the Cobb value and the ink floating time were determined immediately after drying. These results are summarized in Table 1. The leaves were then stored for one day at 23 ° C and 50% relative humidity. The preparation recordings, the Cobb value and the ink floating time were then determined. The measurement results obtained are given in Table 2.
Vergleichsbeispiel Comparative example
Beispiel 1 wurde mit der einzigen Ausnahme wiederholt, daß man an Stelle von 0,1 Gew.-% des Fixiermittels 1 nur 3 Gew.-% Alaun als Fixier- und Fällungsmittel verwendete. Der pH-Wert der Pulpe betrug 7. Die hierbei erhaltenen Ergebnisse sind in den Tabellen 1 und 2 angegeben. Tabelle 1: Sofortleimung
Figure imgf000009_0001
Example 1 was repeated with the only exception that instead of 0.1% by weight of fixative 1, only 3% by weight of alum was used as fixative and precipitant. The pH of the pulp was 7. The results obtained are shown in Tables 1 and 2. Table 1: Immediate sizing
Figure imgf000009_0001
Tabelle 2: Leimung nach Alterung
Figure imgf000009_0002
Table 2: Sizing after aging
Figure imgf000009_0002

Claims

Patentansprüche Claims
1. Verfahren zur Masseleimung von Papier, Pappe und Karton unter Verwendung von Harzleim und eines Fixiermittels zum Fixieren des Harzleims auf den Cellulosefasern, dadurch gekennzeichnet, daß man als1. A process for the mass sizing of paper, cardboard and cardboard using resin glue and a fixing agent for fixing the resin glue on the cellulose fibers, characterized in that as
Fixiermittel kationische Polymerisate einsetzt, die Vinylamineinheiten einpolymerisiert enthalten. Fixing agent uses cationic polymers which contain vinylamine units copolymerized.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß man als 2. The method according to claim 1, characterized in that as
Fixiermittel hydrolysierte Homopolymerisate des N-Vinylformamids mit einem Hydrolysegrad von 0,1 bis 100 % einsetzt.  Fixing agent hydrolyzed homopolymers of N-vinylformamide with a degree of hydrolysis from 0.1 to 100%.
3. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß man als Fixiermittel hydrolysierte Copolymerisate des N-Vinylformamids einsetzt, die bis zu 99 mol-% ethylenisch ungesättigte Monomere aus der Gruppe3. The method according to claim 1, characterized in that the fixing agent used is hydrolyzed copolymers of N-vinylformamide, which contain up to 99 mol% of ethylenically unsaturated monomers from the group
Vinylacetat, Vinylpropionat, der C1- bis C4-Alkylvinylether, N-Vinyl- pyrrolidon, der Ester, Nitrile und Amide vom Acrylsäure oder Methacrylsäure einpolymerisiert enthalten, und bei denen der Hydrolysegrad der einpolymerisierten N-Vinylformamid-Einheiten 0,1 bis 100 % beträgt. Contain vinyl acetate, vinyl propionate, the C 1 - to C 4 -alkyl vinyl ether, N-vinyl pyrrolidone, the esters, nitriles and amides polymerized from acrylic acid or methacrylic acid, and in which the degree of hydrolysis of the polymerized N-vinyl formamide units 0.1 to 100 % is.
4. Verfahren nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß man als Fixiermittel hydrolysierte Polymerisate einsetzt, die erhältlich sind durch Polymerisieren von 4. The method according to any one of claims 1 to 3, characterized in that hydrolyzed polymers are used as fixatives, which are obtainable by polymerizing
(a) 100 bis 10 mol-% N-Vinylformamid und (a) 100 to 10 mol% N-vinylformamide and
(b) 0 bis 90 mol-% Vinylacetat und/oder Vinylpropionat und anschließende Abspaltung von 0,1 bis 100 % der Formylgruppen aus den einpolymerisierten Einheiten (a) und gegebenenfalls 0,1 bis 100 % der Acetyl- und/oder Propionylgruppen aus den einpolymerisierten Einheiten (b), der Copolymerisate. (b) 0 to 90 mol% of vinyl acetate and / or vinyl propionate and subsequent cleavage of 0.1 to 100% of the formyl groups from the polymerized units (a) and optionally 0.1 to 100% of the acetyl and / or propionyl groups from the polymerized units (b), the copolymers.
5. Verfahren nach einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, daß man auf 100 Gew.-Teile Harzleim 10 bis 300 Gew.-Teile mindestens eines kationischen Polymerisats einsetzt. 5. The method according to any one of claims 1 to 4, characterized in that 10 to 300 parts by weight of at least one cationic polymer is used per 100 parts by weight of resin glue.
6. Verwendung von kationischen Polymerisaten, die Vinylamineinheiten 6. Use of cationic polymers, the vinylamine units
einpolymerisiert enthalten, als Fixiermittel für Harzleim bei der polymerized contain, as a fixative for resin glue in the
Masseleimung von Papier, Pappe und Karton. Bulk sizing of paper, cardboard and cardboard.
PCT/EP1991/001894 1990-10-15 1991-10-04 Paper, paperboard and cardboard internal sizing process WO1992007141A2 (en)

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DE59104096T DE59104096D1 (en) 1990-10-15 1991-10-04 METHOD FOR SIZING PAPER, CARDBOARD AND CARDBOARD.
CA002085348A CA2085348C (en) 1990-10-15 1991-10-04 Paper, paperboard and cardboard internal sizing process
JP51621891A JP3176620B2 (en) 1990-10-15 1991-10-04 Sizing of paper, paperboard and cardboard
EP91917563A EP0553135B1 (en) 1990-10-15 1991-10-04 Paper, paperboard and cardboard internal sizing process
FI931642A FI97405C (en) 1990-10-15 1993-04-13 Procedure for mass gluing of paper, cardboard and cardboard

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DE4322854A1 (en) * 1992-07-14 1994-01-27 Air Prod & Chem Process for the synthesis of oligomeric vinyl amines
WO1999028553A1 (en) * 1997-12-01 1999-06-10 Basf Aktiengesellschaft Method for internally sizing paper, paperboard and cardboard
US6273998B1 (en) 1994-08-16 2001-08-14 Betzdearborn Inc. Production of paper and paperboard
WO2004022851A1 (en) * 2002-08-14 2004-03-18 Basf Aktiengesellschaft Method for the production of cardboard made of cellulose fibres for packaging liquids

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US5519093A (en) * 1994-05-11 1996-05-21 Air Products And Chemicals, Inc. Synthesis of amine functional co-and terpolymers
JP2005171411A (en) * 2003-12-10 2005-06-30 Seiko Pmc Corp Filler-containing paper, and method for producing filler-containing paper

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EP0216387A2 (en) * 1985-09-26 1987-04-01 BASF Aktiengesellschaft Process for preparing vinyl amine-containing water soluble copolymers and their use as wet and dry strength agents for paper
EP0438707A1 (en) * 1990-01-16 1991-07-31 BASF Aktiengesellschaft Process for making paper and board

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EP0105028B1 (en) * 1982-08-25 1986-11-12 Ciba-Geigy Ag Process for sizing paper with anionic, hydrophobic sizing agents and cationic retention agents
CA1283748C (en) * 1986-06-25 1991-04-30 Takaharu Itagaki Vinylamine copolymer, flocculating agent and paper strength increasingagent using the same, as well as process for producing the same
GB8806432D0 (en) * 1988-03-18 1988-04-20 Albright & Wilson Paper sizing methods & compositions

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EP0216387A2 (en) * 1985-09-26 1987-04-01 BASF Aktiengesellschaft Process for preparing vinyl amine-containing water soluble copolymers and their use as wet and dry strength agents for paper
EP0438707A1 (en) * 1990-01-16 1991-07-31 BASF Aktiengesellschaft Process for making paper and board

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4322854A1 (en) * 1992-07-14 1994-01-27 Air Prod & Chem Process for the synthesis of oligomeric vinyl amines
DE4322854C2 (en) * 1992-07-14 1998-07-09 Air Prod & Chem Process for the synthesis of oligomeric and polymeric vinylamines
US6273998B1 (en) 1994-08-16 2001-08-14 Betzdearborn Inc. Production of paper and paperboard
WO1999028553A1 (en) * 1997-12-01 1999-06-10 Basf Aktiengesellschaft Method for internally sizing paper, paperboard and cardboard
WO2004022851A1 (en) * 2002-08-14 2004-03-18 Basf Aktiengesellschaft Method for the production of cardboard made of cellulose fibres for packaging liquids

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