CA2448113A1 - Polymer and use thereof in the production of paper and board - Google Patents
Polymer and use thereof in the production of paper and board Download PDFInfo
- Publication number
- CA2448113A1 CA2448113A1 CA002448113A CA2448113A CA2448113A1 CA 2448113 A1 CA2448113 A1 CA 2448113A1 CA 002448113 A CA002448113 A CA 002448113A CA 2448113 A CA2448113 A CA 2448113A CA 2448113 A1 CA2448113 A1 CA 2448113A1
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- Prior art keywords
- paper
- strength
- cationic
- starch
- web
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- Abandoned
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 13
- 229920000642 polymer Polymers 0.000 title description 4
- 239000000654 additive Substances 0.000 claims abstract description 24
- 230000000996 additive effect Effects 0.000 claims abstract description 14
- 239000005017 polysaccharide Substances 0.000 claims abstract description 13
- 239000000178 monomer Substances 0.000 claims abstract description 12
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 12
- -1 cationic polysaccharide Chemical class 0.000 claims abstract description 10
- 150000004676 glycans Chemical class 0.000 claims abstract description 9
- 239000007787 solid Substances 0.000 claims abstract description 8
- 125000002348 vinylic group Chemical group 0.000 claims abstract description 5
- 229920002472 Starch Polymers 0.000 claims description 35
- 235000019698 starch Nutrition 0.000 claims description 35
- 239000008107 starch Substances 0.000 claims description 34
- 238000006467 substitution reaction Methods 0.000 claims description 5
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- 239000007858 starting material Substances 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 abstract description 25
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract description 8
- 229920001577 copolymer Polymers 0.000 abstract description 4
- 239000002253 acid Substances 0.000 abstract description 2
- 239000000123 paper Substances 0.000 description 28
- 238000007792 addition Methods 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 8
- 239000000835 fiber Substances 0.000 description 7
- 229920001131 Pulp (paper) Polymers 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011087 paperboard Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N alpha-ketodiacetal Natural products O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 229920002401 polyacrylamide Polymers 0.000 description 3
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 150000000703 Cerium Chemical class 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 229940015043 glyoxal Drugs 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229940001584 sodium metabisulfite Drugs 0.000 description 2
- 235000010262 sodium metabisulphite Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920000945 Amylopectin Polymers 0.000 description 1
- 229920000856 Amylose Polymers 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001720 carbohydrates Chemical group 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 150000002303 glucose derivatives Chemical group 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 150000004804 polysaccharides Polymers 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
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
- D21H17/21—Macromolecular organic compounds of natural origin; Derivatives thereof
- D21H17/24—Polysaccharides
- D21H17/28—Starch
- D21H17/29—Starch cationic
Landscapes
- Paper (AREA)
- Extrusion Of Metal (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Graft Or Block Polymers (AREA)
Abstract
As additive for the production of paper and board to improve the strength of a wet web a copolymer stabilized with a cationic polysaccharide is proposed in which copolymer an acrylamide of metacrylamide, vinylic craboxyl acid and optionally other vinylic monomers are used as monomers. The west strength of a web means the strength of a paper or board web during production at a dry solids content of 20-60%. The additive according to the invention improves, in addition to the wet strength of the web, also the surface resistance of the product. Compared to the additives of the prior art, a small relative ratio of the number of the side chains to the cationic groups is used, because a polysaccharide having a higher cationic character provides better stability.
Description
WO 02/09128 PCT/F102/00~28 POLYMER AND USE THEREOF IN THE PRODUCTION OF
PAPER AND BOARD
Field of the invention The invention relates to the chemistry of additives for paper making. In particular, the in-S vention relates to a polymer stabilized with a polysaccharide and being generally used as an additive in the production of paper.
Background of the invention Various paper making additives are used to improve the properties of paper.
Water soluble additives such as polyamides, polyamide-epichlorohydrin resins, melamin resins, urea-formaldehyde resins, polyacrylamides as well as preferably starch together with its derivatives are used to improve the strength properties. Starch is an advantageous and preferred raw material of natural origin. The amount of starch required to improve the strength properties is relatively large.
IS
As wood fiber is anionic in character, native starch has a quite low affinity thereto.
Therefore, starch has been chemically modified into the cationic direction.
Starch is cation-ized by attaching substituents having an ionic nitrogen group, such as primary, secondary, tertiary or quaternary ammonium groups, to the carbohydrate backbone. As a measure of Zo the cationic character, the relative ratio of substituted to unsubstituted glucose units, i.e. a degree of substitution, is used. The cationic character can also be expressed as a percentage amount of ionic nitrogen based on the weight of the substituted starch.
Of the strength properties of paper, wet and dry strength properties are to be viewed 25 separately. The dry strength properties are usually improved by adding hydrogen bonds to OH groups of the fiber. The paper strengthening additives of this kind include hydrophilic, water-soluble polymers such as starch, carboxymethylcellulose or synthetic polymers.
These include polyacrylamides of which anionic, cationic and amphoteric are used. Their use is limited by a relative high price.
By the term "wet strength" is usually meant the strength of a finished paper when it be-comes wet, which strength is obtained by the formation of covalent bonds between the WO 02/09128 PCT/FI02/00~28 fibers. This property is of importance when making paper e.g. for filter paper or kitchen paper, and it can be be obtained through reactions between fibers and additives at a high temperature of the drying section of a paper machine. Another wet strength, the strength of a wet web during the production of paper is of great importance for the runnability of the machine, especially when proceeding to a drying section, because the web has been fully supported up to that point. It has been tried to improve this property mainly by increasing the dry solids content of the web in the press section.
In order to combine the properties of polyacrylamides and starches to improve the wet strength of paper, products have been prepared in which acrylamide or metacrylamide and an unsaturated organic acid are polymerized in the presence of starch. In this manner starch is formed to which polymerized side chains have been bound. The starch is preferably cati-onic, having typically a degree of substitution of 0.01 - 0.70.
~5 Japanese patent application JP 2-26944 discloses a polymer of an acrylamide or metacryla mide and methacrylamide acid, prepared in an aqueous solution containing a cationic polysaccharide. In addition to the tensile strength, attempts to improve the tear strength has been made. The cationic character of the polysaccharide is low, and the nitrogen content is 0.4%. In an embodiment, a product is prepared by polymerizing 50 - 95 mol-% of 20 (meth)acrylamide and 5 - 50 mol-% of an a, ~-unsaturated carboxylic acid in an aqueous solution containing 40 - 90 parts per weight of a cationic polysaccbaride. In a further embodiment, a vinylic component to be polymerized is entirely in the form of amide, and after the polymerization, part of the amide groups is hydrolyzed to carboxylic groups.
The goal of Japanese patent application JP 3-213597 is to reduce the bending fracture of paper and paperboard. Said publication describes an amphoteric additive for paper making, which has been prepared by polymerizing 30 - 96 mol-% of methacrylamide or acrylamide and 4 - 50 mol% of an a, /3-unsaturated carboxylic acid or its salt in the presence of cati-30 onic starch, the aqueous solution containing 20 - 90 parts per weight of cationic starch.
The effect has been reported to be due to the advantageous relative ratio of cationic groups WO 02/09128 PCT/FI02/OU~t28 of the starch to the anionic groups of the carboxylic acid, because of which the product is strongly adsorbed on pulp.
In the patent applications described above, the number of the formed side chains of the starch is large in relation to the number of the cationic groups, because low cationic starch was used.
Thus additives are used in the production of paper to improve the complex of fiber and a binder. The rannability of paper in a machine can be improved by web wet strength im-proving agents. The present invention relates particularly to the wet strength of a web, i.e.
to the strength of a paper or paperboard web during the production with a dry solids con-tent of about 20 - 60%.
Disclosure of the invention After intensive researches we have found a copolymer stabilized by a cationic polysaccha-ride to be an advantageous additive in the production of paper and paperboard, in which copolymer acrylamide or metacrylamide, vinylic carboxylic acid and optionally other vi-nylic monomers, e.g. alkylaminoacrylate or metacryIate, are used as monomers.
We have found that for the strength properties, a much smaller ratio of the numbers of side chains to the cationic groups is advantageous compared to the above described prior art, because a polysaccharide having a higher cationic character provides improved stability.
The additive according to the invention improves in addition to the wet strength of a web also the surface resistance of the product. The surface resistance is of particular signifi-cance for printing papers.
For the preparation of an additive for paper and board making according to the invention defined in claim l, a polysaccharide having a strong cationic character is used, which in an aqueous solution is ready for use, and no time-consuming cooking is needed.
The degree of 3o substitution of the cationic polysaccharide is about 0.02 - 0.50. The polysaccharide used is preferably degraded starch. The starch may be any known starch; e.g. potato, corn, waxy WO 02/095128 PCT/FI02/OO.I28 maize, barley, wheat or tapioca starch. In addition to starch, other useful polysaccharides are e.g. dextrine, amylopectin, amylose and mannose.
s In addition, vinylic monomers are used in the product according to this invention. The pro-portion of the monomers calculated on the dry solids content of the starting materials is not more than about 30%, preferably below 20%. Furthermore, at least about 95% of the molar amount of the monomer component is amide.
In the preparation of the product according to the invention, polymerization initiators and l0 pH adjusting agents are used as known in the art. Suitable initiators are e.g. cerium salts, persulfates, hydroperoxides alone or together with a reducing metal salt, or azo com-pounds.
In the following the invention is described by means of examples.
IS
Example 1 Preparation of an additive for the production of paper according to the invention Cationic starch (20% aqueous solution) 860.0 g 2o Water 55.0 g Acrylic acid (80% aqueous solution) 1.2 g Acrylarnide (50% aqueous solution) 38.0 g Tert-butyl hydroperoxide 5.3 g Water 18.3 g 25 Sodium metabisuifite 3.9 g Water 18.3 g Dry solids content 20.0%
Total amount 1000.0 g The cationic starch has a degree of substitution of 0.20; the cationization has been carried out by using a quaternary ammonium compound.
The cationic starch and water are mixed together in a reactor. The pH of the solution is adjusted to 7 by using acetic acid, and 20% of both the tert-butyl hydroperoxide and the sodium metabisulfite aqueous solutions are added. The temperature is raised to 60°C, and a nitrogen atmosphere is arranged in the reactor for the duration of the reaction.
The addition of acrylic acid and acrylamide is started, the addition lasting over a period of 120 minutes.
At the same time, the addition of the remaining amount of the solution of the tert-butyl !0 hydroperoxide and sodium metabisulfite is started, the addition lasting over a period of $0 minutes.
After the additions, the reaction is continued for 120 minutes at 60°C
under agitation. The reaction can be initiated by various initiators, as in the above example by an oxidation-!5 reduction-reagent pair, which includes i.a. a copper sulfate-hydrogen peroxide-pair, or e.g.
by a cerium salt. The catalyst may also be a persulfate or another catalyst commonly used in emulsion polymerization.
Example 2 Testing of handsheets In this test, a paper making pulp based on chemical pulp, mechanical pulp and reject from a paper mill and a laboratory sheeting mould were used. The sheets were prepared in a weight of 60 g/m2. The addition of additives (cationic starch or the product according to example 1 ) was carried out as kg per ton dry pulp.
Control point 1 2 3 4 $ Wet tensile strength kNm/kg Control 0 1.92 Cationic starch 1 1.82 Cationic starch 3 1.93 Product of Examle 1 1 2.12 Product of Example J~ ~ 3 ~ 2.13 1 ~ ~
WO 02/U95128 PCT/FI02/OO.I28 The wet tensile strength was determined freshly on wet sheets (about 35% dry solids).
A paper strip was drawn by a measuring device at constant speed (50 mm/min) and the tensile force required to cause fracturing of the paper was registered. >
The results show that the test product according to the invention improves the wet tensile strength of the sheets while the cationic starch alone does not.
Example 3 1o Laboratory sheets are prepared from a pulp consisting of 80% mechanical pulp and 20%
chemical pulp. The additions of the additives are given in kg/t. In the Example, the tested sheets were prepared using a fiber orientating sheeting mould in which the machine direc-tion (MD) and the cross direction (CD) can be distinguished.
Control point 1 2 3 4 Wet tensile Wet tensile strength strength MD kNm/kg CD kNm/kg Cationic starch + 1 + 2.06 1.35 glyoxal Cationic starch 3 2.26 1.35 Product of Exam- 1+1 3.32 1.67 ple 1 + glyoxal Product of Exam- 3 3.21 1.46 ple 1 l5 It can be seen that the product according to the invention significantly improves the wet web strength both in the machine direction and in the cross direction.
Example 4 2o Laboratory sheets are prepared from a pulp consisting of 15% chemical pulp, 20% reject and 55% mechanical pulp, and as filler kaolin, so that the ash level will be 20%. The addi-tions of the additives are given in kg/t of the dry solids of the pulp.
WO 02/095128 PCT/F102100:128 The sheets were prepared to a basis weight of 70 g/mz.
In the preparation of the sheets, also a conventional pulp starch (MT) was used which was added in the amount of 5 kg/t.
Control point 1 2 3 4 Wet tensile Wet tensileIGT-strength strength pick MD kNm/kg CD kNm/kg m/s Zero point 0 2.1 1.2 2.27 Pulp starch 5 2.4 1.2 2.66 MT + Product of 5 + 1 2.4 1.2 2.82 Example 1 MT + Product of S + 2 2.9 1.3 3.45 Example 1 When preparing these sheets, a fiber orientating mould was used. By using the test product, the wet tensile strength was improved mainly in the machine direction when the test product was added in the amount of 2 kg/t.
Also the IGT surface resistance was measured on these sheets, and a slight improvement could also be observed compared to the zero point as well as to the use of the pulp starch alone. The IGT picking indicates how the surface of a paper, which has been printed with a printing ink, is able to resist abrasion before the surface becomes flocked and the fibers can be seen on the surface.
In addition to what is described above, a product according to the invention may be used in paper and cardboard production, for example for stabilizing hydrophobic size dispersions.
Such sizes are e.g. AKD (alkyl ketene dimer) and ASA ( alkenyl succinic anhydride).
Thus, addition of such size dispersions to the pulp also improves the wet web strength.
PAPER AND BOARD
Field of the invention The invention relates to the chemistry of additives for paper making. In particular, the in-S vention relates to a polymer stabilized with a polysaccharide and being generally used as an additive in the production of paper.
Background of the invention Various paper making additives are used to improve the properties of paper.
Water soluble additives such as polyamides, polyamide-epichlorohydrin resins, melamin resins, urea-formaldehyde resins, polyacrylamides as well as preferably starch together with its derivatives are used to improve the strength properties. Starch is an advantageous and preferred raw material of natural origin. The amount of starch required to improve the strength properties is relatively large.
IS
As wood fiber is anionic in character, native starch has a quite low affinity thereto.
Therefore, starch has been chemically modified into the cationic direction.
Starch is cation-ized by attaching substituents having an ionic nitrogen group, such as primary, secondary, tertiary or quaternary ammonium groups, to the carbohydrate backbone. As a measure of Zo the cationic character, the relative ratio of substituted to unsubstituted glucose units, i.e. a degree of substitution, is used. The cationic character can also be expressed as a percentage amount of ionic nitrogen based on the weight of the substituted starch.
Of the strength properties of paper, wet and dry strength properties are to be viewed 25 separately. The dry strength properties are usually improved by adding hydrogen bonds to OH groups of the fiber. The paper strengthening additives of this kind include hydrophilic, water-soluble polymers such as starch, carboxymethylcellulose or synthetic polymers.
These include polyacrylamides of which anionic, cationic and amphoteric are used. Their use is limited by a relative high price.
By the term "wet strength" is usually meant the strength of a finished paper when it be-comes wet, which strength is obtained by the formation of covalent bonds between the WO 02/09128 PCT/FI02/00~28 fibers. This property is of importance when making paper e.g. for filter paper or kitchen paper, and it can be be obtained through reactions between fibers and additives at a high temperature of the drying section of a paper machine. Another wet strength, the strength of a wet web during the production of paper is of great importance for the runnability of the machine, especially when proceeding to a drying section, because the web has been fully supported up to that point. It has been tried to improve this property mainly by increasing the dry solids content of the web in the press section.
In order to combine the properties of polyacrylamides and starches to improve the wet strength of paper, products have been prepared in which acrylamide or metacrylamide and an unsaturated organic acid are polymerized in the presence of starch. In this manner starch is formed to which polymerized side chains have been bound. The starch is preferably cati-onic, having typically a degree of substitution of 0.01 - 0.70.
~5 Japanese patent application JP 2-26944 discloses a polymer of an acrylamide or metacryla mide and methacrylamide acid, prepared in an aqueous solution containing a cationic polysaccharide. In addition to the tensile strength, attempts to improve the tear strength has been made. The cationic character of the polysaccharide is low, and the nitrogen content is 0.4%. In an embodiment, a product is prepared by polymerizing 50 - 95 mol-% of 20 (meth)acrylamide and 5 - 50 mol-% of an a, ~-unsaturated carboxylic acid in an aqueous solution containing 40 - 90 parts per weight of a cationic polysaccbaride. In a further embodiment, a vinylic component to be polymerized is entirely in the form of amide, and after the polymerization, part of the amide groups is hydrolyzed to carboxylic groups.
The goal of Japanese patent application JP 3-213597 is to reduce the bending fracture of paper and paperboard. Said publication describes an amphoteric additive for paper making, which has been prepared by polymerizing 30 - 96 mol-% of methacrylamide or acrylamide and 4 - 50 mol% of an a, /3-unsaturated carboxylic acid or its salt in the presence of cati-30 onic starch, the aqueous solution containing 20 - 90 parts per weight of cationic starch.
The effect has been reported to be due to the advantageous relative ratio of cationic groups WO 02/09128 PCT/FI02/OU~t28 of the starch to the anionic groups of the carboxylic acid, because of which the product is strongly adsorbed on pulp.
In the patent applications described above, the number of the formed side chains of the starch is large in relation to the number of the cationic groups, because low cationic starch was used.
Thus additives are used in the production of paper to improve the complex of fiber and a binder. The rannability of paper in a machine can be improved by web wet strength im-proving agents. The present invention relates particularly to the wet strength of a web, i.e.
to the strength of a paper or paperboard web during the production with a dry solids con-tent of about 20 - 60%.
Disclosure of the invention After intensive researches we have found a copolymer stabilized by a cationic polysaccha-ride to be an advantageous additive in the production of paper and paperboard, in which copolymer acrylamide or metacrylamide, vinylic carboxylic acid and optionally other vi-nylic monomers, e.g. alkylaminoacrylate or metacryIate, are used as monomers.
We have found that for the strength properties, a much smaller ratio of the numbers of side chains to the cationic groups is advantageous compared to the above described prior art, because a polysaccharide having a higher cationic character provides improved stability.
The additive according to the invention improves in addition to the wet strength of a web also the surface resistance of the product. The surface resistance is of particular signifi-cance for printing papers.
For the preparation of an additive for paper and board making according to the invention defined in claim l, a polysaccharide having a strong cationic character is used, which in an aqueous solution is ready for use, and no time-consuming cooking is needed.
The degree of 3o substitution of the cationic polysaccharide is about 0.02 - 0.50. The polysaccharide used is preferably degraded starch. The starch may be any known starch; e.g. potato, corn, waxy WO 02/095128 PCT/FI02/OO.I28 maize, barley, wheat or tapioca starch. In addition to starch, other useful polysaccharides are e.g. dextrine, amylopectin, amylose and mannose.
s In addition, vinylic monomers are used in the product according to this invention. The pro-portion of the monomers calculated on the dry solids content of the starting materials is not more than about 30%, preferably below 20%. Furthermore, at least about 95% of the molar amount of the monomer component is amide.
In the preparation of the product according to the invention, polymerization initiators and l0 pH adjusting agents are used as known in the art. Suitable initiators are e.g. cerium salts, persulfates, hydroperoxides alone or together with a reducing metal salt, or azo com-pounds.
In the following the invention is described by means of examples.
IS
Example 1 Preparation of an additive for the production of paper according to the invention Cationic starch (20% aqueous solution) 860.0 g 2o Water 55.0 g Acrylic acid (80% aqueous solution) 1.2 g Acrylarnide (50% aqueous solution) 38.0 g Tert-butyl hydroperoxide 5.3 g Water 18.3 g 25 Sodium metabisuifite 3.9 g Water 18.3 g Dry solids content 20.0%
Total amount 1000.0 g The cationic starch has a degree of substitution of 0.20; the cationization has been carried out by using a quaternary ammonium compound.
The cationic starch and water are mixed together in a reactor. The pH of the solution is adjusted to 7 by using acetic acid, and 20% of both the tert-butyl hydroperoxide and the sodium metabisulfite aqueous solutions are added. The temperature is raised to 60°C, and a nitrogen atmosphere is arranged in the reactor for the duration of the reaction.
The addition of acrylic acid and acrylamide is started, the addition lasting over a period of 120 minutes.
At the same time, the addition of the remaining amount of the solution of the tert-butyl !0 hydroperoxide and sodium metabisulfite is started, the addition lasting over a period of $0 minutes.
After the additions, the reaction is continued for 120 minutes at 60°C
under agitation. The reaction can be initiated by various initiators, as in the above example by an oxidation-!5 reduction-reagent pair, which includes i.a. a copper sulfate-hydrogen peroxide-pair, or e.g.
by a cerium salt. The catalyst may also be a persulfate or another catalyst commonly used in emulsion polymerization.
Example 2 Testing of handsheets In this test, a paper making pulp based on chemical pulp, mechanical pulp and reject from a paper mill and a laboratory sheeting mould were used. The sheets were prepared in a weight of 60 g/m2. The addition of additives (cationic starch or the product according to example 1 ) was carried out as kg per ton dry pulp.
Control point 1 2 3 4 $ Wet tensile strength kNm/kg Control 0 1.92 Cationic starch 1 1.82 Cationic starch 3 1.93 Product of Examle 1 1 2.12 Product of Example J~ ~ 3 ~ 2.13 1 ~ ~
WO 02/U95128 PCT/FI02/OO.I28 The wet tensile strength was determined freshly on wet sheets (about 35% dry solids).
A paper strip was drawn by a measuring device at constant speed (50 mm/min) and the tensile force required to cause fracturing of the paper was registered. >
The results show that the test product according to the invention improves the wet tensile strength of the sheets while the cationic starch alone does not.
Example 3 1o Laboratory sheets are prepared from a pulp consisting of 80% mechanical pulp and 20%
chemical pulp. The additions of the additives are given in kg/t. In the Example, the tested sheets were prepared using a fiber orientating sheeting mould in which the machine direc-tion (MD) and the cross direction (CD) can be distinguished.
Control point 1 2 3 4 Wet tensile Wet tensile strength strength MD kNm/kg CD kNm/kg Cationic starch + 1 + 2.06 1.35 glyoxal Cationic starch 3 2.26 1.35 Product of Exam- 1+1 3.32 1.67 ple 1 + glyoxal Product of Exam- 3 3.21 1.46 ple 1 l5 It can be seen that the product according to the invention significantly improves the wet web strength both in the machine direction and in the cross direction.
Example 4 2o Laboratory sheets are prepared from a pulp consisting of 15% chemical pulp, 20% reject and 55% mechanical pulp, and as filler kaolin, so that the ash level will be 20%. The addi-tions of the additives are given in kg/t of the dry solids of the pulp.
WO 02/095128 PCT/F102100:128 The sheets were prepared to a basis weight of 70 g/mz.
In the preparation of the sheets, also a conventional pulp starch (MT) was used which was added in the amount of 5 kg/t.
Control point 1 2 3 4 Wet tensile Wet tensileIGT-strength strength pick MD kNm/kg CD kNm/kg m/s Zero point 0 2.1 1.2 2.27 Pulp starch 5 2.4 1.2 2.66 MT + Product of 5 + 1 2.4 1.2 2.82 Example 1 MT + Product of S + 2 2.9 1.3 3.45 Example 1 When preparing these sheets, a fiber orientating mould was used. By using the test product, the wet tensile strength was improved mainly in the machine direction when the test product was added in the amount of 2 kg/t.
Also the IGT surface resistance was measured on these sheets, and a slight improvement could also be observed compared to the zero point as well as to the use of the pulp starch alone. The IGT picking indicates how the surface of a paper, which has been printed with a printing ink, is able to resist abrasion before the surface becomes flocked and the fibers can be seen on the surface.
In addition to what is described above, a product according to the invention may be used in paper and cardboard production, for example for stabilizing hydrophobic size dispersions.
Such sizes are e.g. AKD (alkyl ketene dimer) and ASA ( alkenyl succinic anhydride).
Thus, addition of such size dispersions to the pulp also improves the wet web strength.
Claims (6)
1. An additive for the production of paper and board, containing a product polymerized from at least one vinylic monomer in the presence of a cationic saccharide, characterized in that the cationic polysaccharide has a degree of substitution of 0.02 -0.50 and that monomers in the amount of up to 30% calculated on the dry weight of the starting materi-als are used in the polymerization, whereby at least 95 % of the molar amount of the monomer component is amide.
2. The additive according to claim 1, characterized in that up to 5% of the molar amount of the monomer component is vinylic carboxylic acid.
3. The additive according to claim 1 or 2, characterized in that monomers in the amount of up to 20 % calculated on the dry weight of the starting materials are used in the polym-erization.
4. The additive according any of claims 1 to 3, characterized in that the polysaccharide is degraded starch.
5. A use of the additive according to claim 1 in the production of paper and board.
6. The use according to claim 5, characterized in that the additive is added in an amount of 1-3 kg per ton of the dry solids of the pulp.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FI20011085A FI113968B (en) | 2001-05-23 | 2001-05-23 | Solution polymer stabilized with a cationic polysaccharide |
FI20011085 | 2001-05-23 | ||
PCT/FI2002/000428 WO2002095128A1 (en) | 2001-05-23 | 2002-05-20 | Polymer and use thereof in the production of paper and board |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2448113A1 true CA2448113A1 (en) | 2002-11-28 |
Family
ID=8561260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002448113A Abandoned CA2448113A1 (en) | 2001-05-23 | 2002-05-20 | Polymer and use thereof in the production of paper and board |
Country Status (9)
Country | Link |
---|---|
US (1) | US20040149412A1 (en) |
EP (1) | EP1392919B1 (en) |
AT (1) | ATE459752T1 (en) |
CA (1) | CA2448113A1 (en) |
DE (1) | DE60235539D1 (en) |
ES (1) | ES2340840T3 (en) |
FI (1) | FI113968B (en) |
PT (1) | PT1392919E (en) |
WO (1) | WO2002095128A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2008128835A (en) | 2005-12-15 | 2010-01-20 | Дау Глобал Текнолоджиз Инк. (Us) | IMPROVED CELLULOSE PRODUCTS CONTAINING AN ADDITIVE COMPOSITION |
US8916640B2 (en) | 2006-07-06 | 2014-12-23 | Dow Global Technologies Llc | Blended polyolefin dispersions |
US8476326B2 (en) * | 2006-09-22 | 2013-07-02 | Dow Global Technologies Llc | Fibrillated polyolefin foam |
EP2543690A3 (en) | 2007-09-28 | 2013-10-30 | Dow Global Technologies LLC | Fiber coated with a dispersion of higher crystallinity olefin |
KR101513388B1 (en) | 2011-04-28 | 2015-04-17 | 휴렛-팩커드 디벨롭먼트 컴퍼니, 엘.피. | Media used in digital high speed inkjet web press printing |
BR112018013682B1 (en) | 2016-03-01 | 2023-03-28 | Kemira Oyj | POLYMER COMPOSITION, USE AND SURFACE IRONING COMPOSITION |
JP7047310B2 (en) * | 2017-09-28 | 2022-04-05 | 荒川化学工業株式会社 | Paper strength enhancer and paper |
CN109749012A (en) * | 2019-01-24 | 2019-05-14 | 湖北中之天科技股份有限公司 | A kind of production method of the environment-friendly type without chlorine polyacrylamide wet strength agent and the application in papermaking |
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US3006806A (en) * | 1957-02-15 | 1961-10-31 | Olin Mathieson | Sized paper and process therefor |
JPS5691075A (en) * | 1979-12-26 | 1981-07-23 | Kao Corp | Size composition |
EP0054231B1 (en) * | 1980-12-12 | 1984-02-15 | Bayer Ag | Paper-sizing agents and a process for their preparation |
US4372814A (en) * | 1981-05-13 | 1983-02-08 | United States Gypsum Company | Paper having mineral filler for use in the production of gypsum wallboard |
US4684708A (en) * | 1985-03-11 | 1987-08-04 | Akzo N.V. | Cationic grafted starch copolymers |
DE3702712A1 (en) * | 1987-01-30 | 1988-08-11 | Basf Ag | SIZING AGENT FOR PAPER BASED ON FINE-PARTED AQUEOUS DISPERSIONS |
JP2622965B2 (en) * | 1987-03-02 | 1997-06-25 | 星光化学工業株式会社 | Papermaking additives |
US4866151A (en) * | 1987-03-25 | 1989-09-12 | National Starch And Chemical Corporation | Polysaccharide graft polymers containing acetal groups and their conversion to aldehyde groups |
IT1224421B (en) * | 1987-12-29 | 1990-10-04 | Lamberti Flli Spa | MODIFIED GALATTOMANNANS AND REALIVE PREPARATION PROCEDURE |
JP2620806B2 (en) * | 1988-07-11 | 1997-06-18 | 星光化学工業株式会社 | Papermaking additives and papermaking methods |
US4954220A (en) * | 1988-09-16 | 1990-09-04 | E. I. Du Pont De Nemours And Company | Polysilicate microgels as retention/drainage aids in papermaking |
US5338406A (en) * | 1988-10-03 | 1994-08-16 | Hercules Incorporated | Dry strength additive for paper |
US5049634A (en) * | 1989-09-22 | 1991-09-17 | National Starch And Chemical Investment Holding Corporation | Derivatized and/or crosslinked products from acetal- and aldehyde-containing polysaccharide graft polymers |
US5122231A (en) * | 1990-06-08 | 1992-06-16 | Cargill, Incorporated | Cationic cross-linked starch for wet-end use in papermaking |
DE4127733A1 (en) * | 1991-08-22 | 1993-02-25 | Basf Ag | Graft polymers of natural substances containing saccharide structures or derivatives thereof and ethylenically unsaturated compounds and their use. |
US5695609A (en) * | 1992-01-20 | 1997-12-09 | Kemira Oy | Process for producing paper |
JP2928785B2 (en) * | 1993-10-08 | 1999-08-03 | 星光化学工業株式会社 | Papermaking additives |
US5824190A (en) * | 1995-08-25 | 1998-10-20 | Cytec Technology Corp. | Methods and agents for improving paper printability and strength |
DE19610995C2 (en) * | 1996-03-21 | 2002-12-19 | Betzdearborn Inc | Paper sizing agents and processes |
GB9625006D0 (en) * | 1996-11-30 | 1997-01-15 | Roe Lee Paper Chemicals Compan | 'One-shot'rosin emulsion including starch derivative for paper sizing |
US5859128A (en) * | 1997-10-30 | 1999-01-12 | E. I. Du Pont De Nemours And Company | Modified cationic starch composition for removing particles from aqueous dispersions |
JP3876522B2 (en) * | 1998-02-20 | 2007-01-31 | 星光Pmc株式会社 | Papermaking paper strength enhancer and method for producing strong paper |
FI107174B (en) * | 1998-07-10 | 2001-06-15 | Raisio Chem Oy | Additive composition for papermaking |
US6451170B1 (en) * | 2000-08-10 | 2002-09-17 | Cargill, Incorporated | Starch compositions and methods for use in papermaking |
-
2001
- 2001-05-23 FI FI20011085A patent/FI113968B/en not_active IP Right Cessation
-
2002
- 2002-05-20 WO PCT/FI2002/000428 patent/WO2002095128A1/en not_active Application Discontinuation
- 2002-05-20 CA CA002448113A patent/CA2448113A1/en not_active Abandoned
- 2002-05-20 PT PT02771660T patent/PT1392919E/en unknown
- 2002-05-20 US US10/478,138 patent/US20040149412A1/en not_active Abandoned
- 2002-05-20 DE DE60235539T patent/DE60235539D1/en not_active Expired - Lifetime
- 2002-05-20 AT AT02771660T patent/ATE459752T1/en active
- 2002-05-20 ES ES02771660T patent/ES2340840T3/en not_active Expired - Lifetime
- 2002-05-20 EP EP02771660A patent/EP1392919B1/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE60235539D1 (en) | 2010-04-15 |
WO2002095128A1 (en) | 2002-11-28 |
ATE459752T1 (en) | 2010-03-15 |
PT1392919E (en) | 2010-03-26 |
FI20011085A0 (en) | 2001-05-23 |
FI20011085A (en) | 2002-11-24 |
FI113968B (en) | 2004-07-15 |
EP1392919B1 (en) | 2010-03-03 |
US20040149412A1 (en) | 2004-08-05 |
EP1392919A1 (en) | 2004-03-03 |
WO2002095128A9 (en) | 2003-01-23 |
ES2340840T3 (en) | 2010-06-10 |
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