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EP0019170A1 - Mélange de liants pour des compositions de couchage de papier - Google Patents

Mélange de liants pour des compositions de couchage de papier Download PDF

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Publication number
EP0019170A1
EP0019170A1 EP80102414A EP80102414A EP0019170A1 EP 0019170 A1 EP0019170 A1 EP 0019170A1 EP 80102414 A EP80102414 A EP 80102414A EP 80102414 A EP80102414 A EP 80102414A EP 0019170 A1 EP0019170 A1 EP 0019170A1
Authority
EP
European Patent Office
Prior art keywords
weight
parts
copolymer
acrylic acid
percent
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
EP80102414A
Other languages
German (de)
English (en)
Other versions
EP0019170B1 (fr
Inventor
Kurt Dr. Wendel
Guenther Dr. Addicks
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
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
Application filed by BASF SE filed Critical BASF SE
Priority to AT80102414T priority Critical patent/ATE2447T1/de
Publication of EP0019170A1 publication Critical patent/EP0019170A1/fr
Application granted granted Critical
Publication of EP0019170B1 publication Critical patent/EP0019170B1/fr
Expired legal-status Critical Current

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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
    • D21H19/00—Coated paper; Coating material
    • D21H19/36—Coatings with pigments
    • D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
    • D21H19/56—Macromolecular organic compounds or oligomers thereof obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H19/58—Polymers or oligomers of diolefins, aromatic vinyl monomers or unsaturated acids or derivatives thereof

Definitions

  • the pigment lines produced in this way have an insufficient printability in gravure printing, which manifests itself in the fact that the gravure printing ink, especially in the semitones, is not transferred to the stitch sufficiently uniformly, and so-called “missing dots” occur in the print.
  • emulsion copolymers A which contain 40 to 70 parts by weight of styrene, 30 to 60 parts by weight of an ester of acrylic or methacrylic acid with alcohols which contain 2 to 12 carbon atoms in the chain, and optionally up to 10 parts of other ethylenically unsaturated -Copolymerizable compounds and an emulsion copolymer B from 15 to 55 percent by weight acrylic and / or methacrylic acid, optionally up to 10 percent by weight acrylic and / or methacrylamide and 85 to 45 percent by weight other monomers forming water-insoluble homopolymers, of which at least 20 Ge percent by weight, based on these hydrophobic monomers, are esters of acrylic acid or methacrylic acid with alcohols which contain 1 to 4 carbon atoms.
  • the binder mixture contains 5 to 40 parts by weight of at least one copolymer B and 95 to 60 parts by weight of at least one copolymer A.
  • the paper coating colors which are produced using these binder mixtures meet the processing requirements, but no longer meet the increased demands on the printability of them coated papers in rotogravure.
  • the object of the invention is to provide a binder which, in comparison to known binders, can be used in a smaller amount for the preparation of paper coating slips and which results in coated papers which, particularly in magazine gravure printing, result in a better print loss.
  • a binder mixture for paper coating slips based on aqueous dispersions of 95 to 70 parts by weight of an emulsion copolymer A which contains acrylic acid esters and ethylenically unsaturated carboxylic acids in copolymerized form, and 5 to 30 parts by weight of a copolymer B of 15 to 55% by weight acrylic and or or methacrylic acid, optionally up to 10 percent by weight.
  • ' 4 carbon atoms are, if the copolymer A 80 to 96 weight percent ester of acrylic acid with contains copolymerized monohydric C 2 to C 8 alcohols, 0 to 19.5 percent by weight of styrene, acrylonitrile and / or methyl methacrylate, and 0.5 to 10 percent by weight of other monomers which form water-soluble homopolymers.
  • the copolymer A of the binder mixture contains, as an essential component, acrylic acid esters with monohydric alcohols which have 2 to 8 carbon atoms. Specifically, these are, for example, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-, iso- and / or tert-butyl acrylate and 2-ethylhexyl acrylate. Those acrylic acid esters which are derived from isobutanol and n-butanol are preferably used to construct copolymers A.
  • copolymer A up to 50% by weight of the esters of acrylic acid and monohydric C 2 -C 8 -alcohols can be replaced by methyl acrylate and / or by esters of methacrylic acid and monohydric C 2 -C 8 -alcohols.
  • the acrylic acid esters make up 80 to 96, preferably 80 to 90 percent by weight of the emulsion copolymers A.
  • the copolymers A may contain, as a further constituent, a monomer from the group styrene, methyl methacrylate or acrylonitrile. These monomers make up 0 to 19.5, preferably 3 to 15 percent by weight of the copolymers A.
  • Another essential component of the copolymers A are water-soluble homopolymers forming monomers.
  • these are, for example, ethylenically unsaturated C 3 to C 5 carboxylic acids, such as acrylic acid, methacrylic acid, maleic acid or crotonic acid, the corresponding acid amides of the ethylenically unsaturated carboxylic acids, for example acrylic amide and methacrylamide, half-esters and half-amides of maleic acid as well as strongly acidic monomeric compounds such as vinylsulfonic acid, styrene-p-sulfonic acid, acrylamidopropanesulfonic acid, and sodium vinylsulfonate.
  • carboxylic acids such as acrylic acid, methacrylic acid, maleic acid or crotonic acid
  • the corresponding acid amides of the ethylenically unsaturated carboxylic acids for example acrylic amide and methacrylamide, half-esters and half-amides of maleic acid as well as strongly
  • the copolymer A preferably contains 1.0 to 5% of the water-soluble homopolymers forming monomers, of which acrylic acid, acrylamide and methacrylamide or mixtures thereof are preferably used.
  • the glass transition temperature of copolymer A can be between -20 and + 10 ° C. (For the definition of the glass transition temperature see P.J. Flory, Principles of Polymer Chemistry, Cornell University Press, Ithaka, New York, 1953, page 56.)
  • the emulsion copolymers B are known from DE-PS 12 58 728. These copolymers contain 15 to 55 percent by weight of acrylic acid or methacrylic acid, 0 to 10 percent by weight, in particular 2 to 6 percent by weight, acrylamide or methacrylamide and 85 to 45 percent by weight of hydrophobic water-insoluble homopolymers, of which at least 20 percent by weight of esters of acrylic acid or methacrylic acid with aliphatic C. 1 to C 4 alcohols. are.
  • Suitable hydrophobic, water-insoluble homopolymers are, for example, acrylic acid and methacrylic acid esters of higher aliphatic, cycloaliphatic or aromatic hydroxyl compounds, preferably vinyl acetate, vinyl propionate, methyl acrylate, ethyl acrylate and acrylonitrile.
  • the copolymers B preferably contain acrylic acid and / or methacrylic acid and exclusively or predominantly acrylic acid and methacrylic acid esters of monohydric alcohols having 1 to 4 carbon atoms.
  • Terpolymeri are also preferred sate into consideration that still contain copolymerized acrylonitrile, vinyl acetate or acrylamide or methacrylamide.
  • the copolymers A and B can be prepared by polymerizing the monomers in an aqueous emulsion by processes known per se using the customary anionic or nonionic emulsifiers in the presence of polymerization initiators.
  • Suitable emulsifiers are, for example, potassium or sodium n-dodecylsulfonic acid, sodium isooctylbenzenesulfonic acid or potassium salts of the sulfuric acid half-esters of long-chain alcohols with an even carbon number or the corresponding ethoxylated (for example with 2 to 25 mol of ethylene oxide) products, and 5 to 25 mol of ethylene oxide reacted with iso-phenylphenylene oxide and sodium lauryl sulfate.
  • the emulsifiers are generally used in amounts of 0.5 to 5 percent by weight, based on the monomers to be polymerized.
  • radical-forming compounds such as peroxides, persulfates or azo compounds can be used as polymerization initiators.
  • potassium persulfate, cumene hydroperoxide or hydrogen peroxide are suitable.
  • redox catalysts or with activated initiator systems, for example with a system composed of potassium persulfate and ascorbic acid, sodium oxime methanesulfonate or triethanolamine.
  • the temperatures during the polymerization are in the usual range, for example between 70 and 95 ° C, they can be lower if redox catalysts are used. It is also possible to polymerize at higher temperatures and under pressure.
  • chain transfer agents can be used in the polymerization, for example Dodecyl mercaptan and halogenated hydrocarbons such as chloroform, carbon tetrachloride and tetrachlorethylene.
  • the binder mixture according to the invention contains 95 to 70 parts by weight of the emulsion copolymer A and 5 to 30 parts by weight of the copolymer B. Outside this range, binder mixtures are obtained whose properties are not so advantageous.
  • the paper coating slips contain 3 to 7, preferably 4.5 to 5.5 parts by weight of the binder mixture according to the invention per 100 parts by weight of a finely divided pigment. They can also contain conventional additives, e.g. 0.05 to 3 percent by weight of a dispersant based on low molecular weight polymers of acrylic acid (K value of the polymer between 10 and 25) optical brighteners and conventional auxiliaries such as stearates, shading dyes, foam inhibitors, etc.
  • a dispersant based on low molecular weight polymers of acrylic acid (K value of the polymer between 10 and 25) optical brighteners and conventional auxiliaries such as stearates, shading dyes, foam inhibitors, etc.
  • aqueous dispersions of copolymers A and B are mixed before the coating color is prepared or during the preparation of the coating color.
  • the order in which the individual components are added when preparing the coating color is also irrelevant to the properties of the coating slip or the paper coated with it.
  • the mixture of the two copolymers A and B is notable for an exceptionally high storage stability which exceeds that of the known binder mixtures.
  • the solids content of the dispersions of copolymers A and B can vary within a wide range will.
  • Dispersions with a very high solids content are preferably used.
  • the highly concentrated aqueous polymer dispersions are also easy to handle, for example they can be pumped.
  • a base such as ammonia, sodium carbonate, an amine or sodium hydroxide solution
  • the viscosity increases.
  • a barely flowable paste can be obtained by neutralizing the copolymers.
  • the finished paper coating slips can be applied to base papers by all known methods. Due to the high shear stability, the paper coating slips can be processed on high-speed roller or doctor coating systems. They are mainly used for the production of such papers that are printed in magazine gravure. A better print loss is obtained on these papers than on those papers, for which known paper coating slips were used. The better quality of the printing loss in gravure printing is determined based on missing d-ots.
  • the binder mixture according to the invention for the production of paper coating slips, based on pigment, less binder is required than is the case with the known binder mixtures. Despite the reduced binder content in the paper coating slips obtained using the binder mixture according to the invention, there is no dusting of the pigment coating on the papers coated with these paper coating slips.
  • the parts mentioned in the following examples are parts by weight.
  • Feed 1 consists of 460 parts of water, 32 parts of a 28% solution of the sodium salt of a sulfated reaction product from a C 12 / C 14 alcohol which has been reacted with 3 mol of ethylene oxide, 738 parts (82%) of isobutyl acrylate, 126 parts (14 %) Methyl methacrylate, 18 parts (2%) acrylic acid and 18 parts (2%) methacrylamide.
  • Feed 2 consists of 200 parts of water and 4.5 parts of potassium peroxydisulfate.
  • the procedure is essentially the same as for the preparation of the copolymer A 1, but a terpolymer of the composition 96% isobutyl acrylate, 2.5% acrylic acid and 1.5% acrylamide is prepared.
  • This copolymer is prepared analogously to copolymer A 1, except that it is composed of 85 isobutyl acrylate, 12% acrylonitrile, 1.5% acrylic acid and 1.5% methacrylamide.
  • a copolymer B 1 is prepared which is composed of 75% ethyl acrylate, 5% acrylamide and 20% acrylic acid.
  • aqueous solution of 0.3 parts of sodium polyacrylate with a K value of 12 100 parts of a commercially available spreading clay are stirred in using a high-speed stirrer. 9.6 parts of a mixture consisting of 80 parts of a 50% aqueous dispersion of copolymer A 3 and 20 parts of a 45% aqueous dispersion of copolymer B 1 are added as binders, and the coating color is adjusted to a pH value by adding sodium hydroxide solution 8.5 set. With a solids content of 58%, the coating slip has a viscosity of 1400 mPas (measured with a Brookfield viscometer at 100 rpm).
  • the paper coating slip produced in this way is applied to a paper which is composed of 55% groundwood, 45% bleached sulfate pulp, an ash content of 6% and a basis weight of 38 g / m 2 h with the aid of a doctor coating system at a speed of 800 m / min at.
  • the paper is coated on both sides.
  • the coating is 10 g / m 2 and side.
  • the paper which is satinised in the supercalender at a speed of 300 m / min and 2000 N / cm line printing, has good gloss and smoothness and excellent printability.
  • a print that is applied with the help of a Haindl laboratory gravure printing device has, in semitones, less than 10 missing dots on an area of 30 cm 2 . The missing dots were determined by visually counting the missing areas.
  • the paper coating slip is prepared as described in Example 1, except that 10.2 parts of a binder mixture of 80 parts of the 50% aqueous dispersion of copolymer A 2 and 20 parts of the 45%, based on 100 parts of a commercially available coating clay, are used. aqueous dispersion of the copolymer B 1.
  • the coating color has a solids content of 56% and a viscosity of 1300 mPas (Brookfield viscometer 100 rpm).
  • the paper which has been coated and satinized as in Example 1 has less than 10 missing dots on an area of 30 cm 2 in halftone gravure printing.
  • a paper coating slip is produced according to the instructions given in Example 1, but based on 100 parts of a commercially available coating clay, 10.2 parts of a binder mixture composed of 75 parts of the 50% aqueous dispersion of copolymer A 1 and 25 parts of the 45% aqueous dispersion of copolymer B 1.
  • the viscosity of the coating color at a solids content of 56% is 1300 mPas (Brookfield viscometer 100 Rpm).
  • a paper coating slip is prepared as described in Example 1, but 10.2 parts of a mixture of 80 parts of a 50% aqueous dispersion of a copolymer of 55% isobutyl acrylate, 42% styrene, 1 are used as the binder, based on 100 parts of coating clay , 5% acrylic acid and 1.5% methacrylamide and 20 parts of the 45% dispersion of the copolymer B 1.
  • the coating color has a solids content of 56% and a viscosity of 1200 mPas (Brookfield viscometer 100 rpm).
  • the paper coated and satined with this paper coating slip in accordance with the specification given in Example 1 has more than 20 missing dots on an area of 30 cm 2 in halftone gravure printing.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Paper (AREA)
EP80102414A 1979-05-17 1980-05-05 Mélange de liants pour des compositions de couchage de papier Expired EP0019170B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT80102414T ATE2447T1 (de) 1979-05-17 1980-05-05 Bindemittelgemisch fuer papierstreichmassen.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19792919937 DE2919937A1 (de) 1979-05-17 1979-05-17 Bindemittelgemisch fuer papierstreichmassen
DE2919937 1979-05-17

Publications (2)

Publication Number Publication Date
EP0019170A1 true EP0019170A1 (fr) 1980-11-26
EP0019170B1 EP0019170B1 (fr) 1983-02-09

Family

ID=6070970

Family Applications (1)

Application Number Title Priority Date Filing Date
EP80102414A Expired EP0019170B1 (fr) 1979-05-17 1980-05-05 Mélange de liants pour des compositions de couchage de papier

Country Status (4)

Country Link
EP (1) EP0019170B1 (fr)
AT (1) ATE2447T1 (fr)
DE (2) DE2919937A1 (fr)
FI (1) FI71570C (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999000437A1 (fr) * 1997-06-27 1999-01-07 Basf Aktiengesellschaft Pates pour le couchage du papier a base de liants aux derives de n-vinylformamide
WO2008095878A3 (fr) * 2007-02-08 2008-09-25 Basf Se Liants hydrosolubles pour pâtes de couchage de papier

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040151886A1 (en) 2000-03-06 2004-08-05 Bobsein Barrett Richard Binder composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1264945B (de) * 1963-11-20 1974-05-30 Bindemittel fuer papierstreichmassen
FR2378896A1 (fr) * 1977-01-28 1978-08-25 Basf Ag Masses de couchage perfectionnees pour le papier

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1264945B (de) * 1963-11-20 1974-05-30 Bindemittel fuer papierstreichmassen
FR2378896A1 (fr) * 1977-01-28 1978-08-25 Basf Ag Masses de couchage perfectionnees pour le papier

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999000437A1 (fr) * 1997-06-27 1999-01-07 Basf Aktiengesellschaft Pates pour le couchage du papier a base de liants aux derives de n-vinylformamide
WO2008095878A3 (fr) * 2007-02-08 2008-09-25 Basf Se Liants hydrosolubles pour pâtes de couchage de papier

Also Published As

Publication number Publication date
FI801564A7 (fi) 1980-11-18
DE3061869D1 (en) 1983-03-17
FI71570B (fi) 1986-10-10
EP0019170B1 (fr) 1983-02-09
DE2919937A1 (de) 1980-11-27
FI71570C (fi) 1987-01-19
ATE2447T1 (de) 1983-03-15

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