EP0187666A1 - Internal sizing process in the manufacture of paper, cardboard, boards and other cellulosic materials - Google Patents
Internal sizing process in the manufacture of paper, cardboard, boards and other cellulosic materials Download PDFInfo
- Publication number
- EP0187666A1 EP0187666A1 EP86100189A EP86100189A EP0187666A1 EP 0187666 A1 EP0187666 A1 EP 0187666A1 EP 86100189 A EP86100189 A EP 86100189A EP 86100189 A EP86100189 A EP 86100189A EP 0187666 A1 EP0187666 A1 EP 0187666A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- resin
- dicyandiamide
- paper
- cationic
- cardboard
- 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
Links
- 238000004513 sizing Methods 0.000 title claims abstract description 27
- 239000000123 paper Substances 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 title claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 239000011111 cardboard Substances 0.000 title claims abstract description 8
- 239000000463 material Substances 0.000 title claims abstract description 8
- 239000011347 resin Substances 0.000 claims abstract description 59
- 229920005989 resin Polymers 0.000 claims abstract description 59
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 claims abstract description 40
- 125000002091 cationic group Chemical group 0.000 claims abstract description 30
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 20
- 230000007935 neutral effect Effects 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 12
- 239000001913 cellulose Substances 0.000 claims abstract description 9
- 229920002678 cellulose Polymers 0.000 claims abstract description 9
- -1 amine salt Chemical class 0.000 claims abstract description 8
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 8
- 150000007524 organic acids Chemical class 0.000 claims abstract description 8
- 239000000049 pigment Substances 0.000 claims abstract description 8
- 239000007859 condensation product Substances 0.000 claims abstract description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 36
- 239000000945 filler Substances 0.000 claims description 21
- 150000001412 amines Chemical class 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims description 2
- 229940088417 precipitated calcium carbonate Drugs 0.000 claims description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 1
- UWTNZVZEAHSTRO-UHFFFAOYSA-N azane;ethane-1,2-diamine Chemical compound N.NCCN UWTNZVZEAHSTRO-UHFFFAOYSA-N 0.000 claims 1
- 238000011049 filling Methods 0.000 abstract description 3
- 159000000013 aluminium salts Chemical class 0.000 abstract 1
- 239000011087 paperboard Substances 0.000 abstract 1
- 239000003292 glue Substances 0.000 description 29
- 235000010216 calcium carbonate Nutrition 0.000 description 17
- 229910000019 calcium carbonate Inorganic materials 0.000 description 16
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 8
- 229940037003 alum Drugs 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 6
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 239000005995 Aluminium silicate Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 5
- 235000012211 aluminium silicate Nutrition 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 239000011436 cob Substances 0.000 description 5
- 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 5
- 239000000047 product Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 235000019270 ammonium chloride Nutrition 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 235000005985 organic acids Nutrition 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 235000019253 formic acid Nutrition 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- NGDLSKPZMOTRTR-OAPYJULQSA-N (4z)-4-heptadecylidene-3-hexadecyloxetan-2-one Chemical compound CCCCCCCCCCCCCCCC\C=C1/OC(=O)C1CCCCCCCCCCCCCCCC NGDLSKPZMOTRTR-OAPYJULQSA-N 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 150000002561 ketenes Chemical class 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 229960001124 trientine Drugs 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- VZTDIZULWFCMLS-UHFFFAOYSA-N ammonium formate Chemical compound [NH4+].[O-]C=O VZTDIZULWFCMLS-UHFFFAOYSA-N 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical group O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
- NKWPZUCBCARRDP-UHFFFAOYSA-L calcium bicarbonate Chemical compound [Ca+2].OC([O-])=O.OC([O-])=O NKWPZUCBCARRDP-UHFFFAOYSA-L 0.000 description 1
- 229910000020 calcium bicarbonate Inorganic materials 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- BBKJIBJUWBIXIL-UHFFFAOYSA-N ethane-1,2-diamine;formic acid Chemical compound OC=O.NCCN BBKJIBJUWBIXIL-UHFFFAOYSA-N 0.000 description 1
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000014380 magnesium carbonate Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- XPVOJYDIBHYVFL-UHFFFAOYSA-N n'-[2-(2-aminoethylamino)ethyl]ethane-1,2-diamine;hydrochloride Chemical compound Cl.NCCNCCNCCN XPVOJYDIBHYVFL-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000011787 zinc oxide 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
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
- D21H17/49—Condensation polymers of aldehydes or ketones with compounds containing hydrogen bound to nitrogen
- D21H17/50—Acyclic compounds
Definitions
- the invention relates to a method for sizing in the production of paper, cardboard, cardboard and other cellulose-containing materials with and without fillers and / or coating pigments under neutral to weakly basic pH conditions.
- Paper production requires a mediator or a fixing agent to bind the resin glue to the fiber surface, since both the resin glue and the cellulose fibers are electronegatively charged and repel each other.
- Alum aluminum sulfate hydrate
- Alum is used almost exclusively for this purpose in the production of the paper in an acidic medium, with the best sizing being achieved at a pH value of 4.5 to 5.5.
- papers produced in this way are not resistant to aging as a result of progressive hydrolysis.
- a modified pseudo-neutral paper making method is described in Japanese Patent Laid-Open No. 83-174,696.
- a dicyandiamide-formaldehyde condensation product is added to the aluminum sulfate as an additional agent.
- this method still has the disadvantage that an expensive diketene resin has to be used.
- European patent application 112 525 proposes a means for neutral sizing of cellulose-containing materials, which consists of water, a in Unlimited water soluble alcohol, alkali or aluminum hydroxide and a saturated or unsaturated fatty acid with 12 to 24 carbon atoms.
- the aim of the neutral paper production process is to largely reduce or eliminate the use of aluminum sulfate and to replace kaolin as filler or pigment with calcium carbonate.
- the latter is less expensive than kaolin and its whiteness exceeds that of kaolin. Due to the more favorable flow behavior of calcium carbonate, higher degrees of filling can also be achieved in the paper. In addition, the corrosion on the machine equipment is reduced and the quality of the paper, in particular its resistance to aging, is significantly improved.
- the present invention is therefore based on the object of developing a paper production process which operates in neutral to weakly basic pH ranges and under these conditions avoids the disadvantages of the previously known processes.
- This object is achieved by a process for sizing in the production of paper, cardboard, cardboard and other cellulose-containing materials with and without fillers and / or pigments by natural or synthetic sizing agents under neutral to weakly basic pH conditions, which is characterized in that one glues with a combination of natural or synthetic sizing agents with a cationic dicyandiamide resin.
- Cationic dicyandiamide resins which have a high positive charge and which are therefore able to precipitate anionic, high molecular weight substances quickly and practically quantitatively have proven to be particularly suitable. These resins are expediently not made too acidic, so that after mixing with the stock suspension the pH does not drop significantly below 7.
- the cationic dicyandiamide resins used according to the invention can be prepared, for example, by reacting 1 mol of dicyandiamide with 1.0 to 4.0 mol of formaldehyde in the presence of 0.1 to 2.0 mol of at least one inorganic or organic acid and / or at least one ammonium or amine salt thereof and optionally up to 0.5 mol of a di- or polyvalent amine.
- Condensation products prepared in this way have pH values of about 3 to about 5, are miscible with water in any ratio and can be used well as an approximately 50% aqueous solution.
- acids such as B. strong inorganic acids such as hydrochloric acid, sulfuric acid or nitric acid.
- weakly acidic organic acids such as. B. formic acid, acetic acid or oxalic acid is used.
- ammonium salt can be used in resin production such.
- B. ammonium salts of strong inorganic acids such as ammonium chloride or ammonium sulfate or ammonium salts of organic acids such as ammonium formate or acetate can be used.
- amine salts salts of organic amines with inorganic or organic acids such as.
- B. ethylenediamine formate or triethylenetetramine hydrochloride can be used.
- the salts mentioned can also be used in a mixture with inorganic or organic acids.
- Divalent or polyvalent aliphatic amines can be used as the amine component to be added. Ethylene diamine, propylene diamine, diethylene triamine and triethylene tetramine are preferably used. Their derivatives substituted on the nitrogen by hydroxyl groups can also be used, such as, for. B. mono- or diethanolamine. If amines are added, their amount is preferably at least 0.05 mol per mol of dicyandiamide.
- Formaldehyde can be used in any form, preferably in the form of its 30 to 40% by weight aqueous solutions.
- Neutral to weakly basic pH values are understood to mean those between pH 6.5 and 8.5, preferably between 7.0 and 8.0.
- the condensation products obtained by the process described are clear, colorless, water-miscible products.
- cationic dicyandiamide resins produced by other processes can also be used within the scope of the invention.
- the amount of cationic dicyandiamide resin to be used is based on the "substance" (cellulose) amount and is generally 0.1 to 10% by weight; 0.2 to 5% by weight of dicyandiamide resin is preferably used, advantageously in the form of an approximately 50% strength aqueous solution.
- glues based on natural or synthetic starting materials can be used.
- Suitable products are e.g. B. rosin, animal glue, casein, starch, waxes, fatty acids and tall resins.
- Synthetic glues are particularly suitable for products based on ketene dimers,
- ketene dimers Polyvinyl alcohols or polyvinyl acetates. Products used as ketene dimers are those which have been prepared on the basis of alkyl-substituted, dimeric ketene with an oxetanone structure, starting from long-chain fatty acids, and which are sold under the brand name Aquapel.
- modified resin glues such as z. B. by implementing z. B. rosin can be obtained with dienophilic acids and are commercially available under the brand name Furtin 3 N / S.
- extremely finely divided dispersions of specially modified, reinforced resins e.g. Furtin BVR 510) can be used with advantage.
- the method according to the invention now surprisingly makes it possible to flocculate and fix it on the fiber by combining cationic dicyandiamide resin with the chemically very different glue components mentioned above. In this way, full or partial sizing of the paper can be achieved with natural, synthetic or modified resin glues without the aid of further aids.
- All fillers and pigments customary in paper production can also be used in the process according to the invention, such as, for. B. kaolin, aluminum silicates, calcium silicates, oxyhydrates of aluminum, talc, satin white, gypsum, barium sulfate, barium carbonate, magnesite, zinc oxide, titanium dioxide.
- calcium carbonate is preferably used. This can consist of finely ground natural calcium carbonate or precipitated calcium carbonate. Calcium carbonate is preferred because its whiteness z. B. exceeds that of kaolin and its favorable flow behavior allows particularly high filling levels in the paper to be achieved. This also has a positive influence on the paper properties: opacity is increased, whiteness is improved, aging resistance is increased and mechanical properties are increased.
- a cationic dicyandiamide-formaldehyde resin 84 parts by weight of dicyandiamide are placed in a stirred vessel equipped with a reflux condenser with 220 parts by weight of 30% strength aqueous formaldehyde and 43 parts by weight of ammonium chloride. At room temperature, 7.7 parts by weight of ethylenediamine (78%) are then added with stirring. The reaction starts immediately and the temperature of the reaction mixture rises to 90 to 95 ° C. The reaction is complete after about 10 minutes. Then water is added to adjust the concentration of 50% by weight of solid in the resin.
- ammonium chloride instead of ammonium chloride, an inorganic or organic acid such as. B. hydrochloric acid or formic acid can be used.
- Leaves are formed on a Rapid-Köthen sheet former using bleached pine pulp with a freeness of 24 ° SR, resin glue (free resin glue Furtin 3N) and 50X aqueous cationic dicyandiamide resin (made from dicyandiamide, formaldehyde, ammonium chloride and ethylenediamine) and thermally applied on cylinders for 3 minutes 120 ° C treated. After the air conditioning, the sizing was determined by the water absorption using the Cobb test (60 sec.) In accordance with DIN 53132. The use of the cationic dicyandiamide resin was compared to alum as a sizing agent, the pH adjusting itself.
- resin glue free resin glue Furtin 3N
- 50X aqueous cationic dicyandiamide resin made from dicyandiamide, formaldehyde, ammonium chloride and ethylenediamine
- Sheet formation using calcium carbonate as a filler Sheet formation using calcium carbonate as a filler.
- the test conditions were the same as in Example 1, but weakly anionic calcium carbonate was added as a filler.
- the weight ratio of pulp to filler was 1: 2.
- the filler was processed in the Ultra Turrax (disperser) for 5 minutes, then mixed with the cellulose for 3 minutes and then the glue and the cationic dicyandiamide resin were added.
- Example 2 The same cationic dicyandiamide resin and the same calcium carbonate quality were used as in Example 2.
- a synthetic product based on diketene (Aquapel 2) was used for sizing. The quality of the sizing was determined using the Cobb test.
- Example 4 The same dicyandiamide resin and the same resin size were used as in Example 4. Weakly anionic calcium carbonate was used as the filler. The sheets were produced in a manner analogous to that given in Example 1.
- Example 6 Using the cationic dicyandiamide resin mentioned in Example 6, the same specially modified resin size and weakly anionic calcium carbonate as filler, sheets were produced in accordance with Example 1, the Cobb values of which are shown in the following table.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Cartons (AREA)
- Wrappers (AREA)
- Steroid Compounds (AREA)
Abstract
Description
Die Erfindung betrifft ein Verfahren zur Leimung bei der Herstellung von Papier, Karton, Pappen und anderen cellulosehaltigen Materialien mit und ohne Füllstoffen und/oder Streichpigmenten unter neutralen bis schwach basischen pH-Bedingungen.The invention relates to a method for sizing in the production of paper, cardboard, cardboard and other cellulose-containing materials with and without fillers and / or coating pigments under neutral to weakly basic pH conditions.
Die Papierherstellung erfordert zur Bindung des Harzleimes auf der Faseroberfläche einen Vermittler bzw. ein Fixiermittel, da sowohl der Harzleim als auch die Cellulosefasern elektronegativ geladen sind und sich gegenseitig abstoßen. Bei der Herstellung des Papieres im sauren Medium wird hierfür fast ausschließlich Alaun (Aluminiumsulfathydrat) verwendet, wobei die beste Leimung bei einem pH-Wert des Stoffes von 4,5 bis 5,5 erzielt wird. So hergestellte Papiere sind jedoch infolge fortschreitender Hydrolyse nicht alterungsbeständig.Paper production requires a mediator or a fixing agent to bind the resin glue to the fiber surface, since both the resin glue and the cellulose fibers are electronegatively charged and repel each other. Alum (aluminum sulfate hydrate) is used almost exclusively for this purpose in the production of the paper in an acidic medium, with the best sizing being achieved at a pH value of 4.5 to 5.5. However, papers produced in this way are not resistant to aging as a result of progressive hydrolysis.
Es wurde deshalb versucht, Papier unter neutralen Bedingungen zu leimen. Die Verwendung von Alaun ist hierbei jedoch nicht möglich, da das Aluminium-Ion in diesem pH-Bereich schnell seine positive Ladung ver- liert und damit den negativ geladenen Leim nur noch unvollständig ausflocken kann.An attempt was therefore made to glue paper under neutral conditions. The use of alum, however, this is not possible because the aluminum ion in this pH range quickly its positive charge ver - lines and can thus flocculate negatively charged glue only incomplete.
Darüberhinaus reagiert Aluminiumsulfat mit dem unter neutralen Bedingungen als Pigment und Füllstoff gerne verwendeten Calciumcarbonat unter Kohlendioxidabspaltung, was zu Schaumentwicklung und Löcherbildung auf der Papierbahn führt. Ausfallendes Calciumsulfat führt zu Ablagerungen an der Maschine, so daß eine störungsfreie Papierherstellung nicht möglich ist. Da für das Aluminiumsulfat bisher kein Ersatz gefunden wurde, kann man auch den üblichen Harzleim bei der Papierherstellung unter neutralen Bedingungen nicht verwenden sondern mußte auf synthetische Leime zurückgreifen, was die Papierherstellung wesentlich verteuerte.In addition, aluminum sulfate reacts with the calcium carbonate, which is often used as a pigment and filler under neutral conditions, with the elimination of carbon dioxide, which leads to foaming and hole formation on the paper web. Failing calcium sulfate leads to deposits on the machine, so that trouble-free paper production is not possible. Since no substitute has yet been found for the aluminum sulfate, the usual resin glue cannot be used in papermaking under neutral conditions, but instead had to use synthetic glue, which made papermaking considerably more expensive.
Einen Ausweg schien die "pseudo-neutral-Fahrweise" unter Verwendung nur geringer Mengen Aluminiumsulfat zu bieten. Dieses wird dem Dünnstoff sehr spät zugesetzt, so daß die oben geschilderten unerwünschten Reaktionen zu keinen Schwierigkeiten führen. Um die verminderte Fällungswirkung des Alauns bei den hierbei vorliegenden pH-Werten von 6,5 bis 7,4 zu kompensieren, müssen aber noch andere kationische Mittel der Stoffsuspension zugegeben werden. Trotzdem besteht immer die Gefahr, daß das durch Reaktion von entbundener Kohlensäure mit Calciumcarbonat gebildete Calciumhydrogencarbonat im Laufe des Papierherstellungsverfahrens wieder zu Calciumcarbonat und Kohlendioxid zerfällt und Calciumcarbonatablagerungen entstehen, die zu Produktionsunterbrechungen führen.The "pseudo-neutral driving style" using only small amounts of aluminum sulfate seemed to offer a way out. This is added to the thin material very late, so that the undesired reactions described above do not lead to any difficulties. In order to compensate for the reduced precipitation effect of the alum at the present pH values of 6.5 to 7.4, other cationic agents have to be added to the pulp suspension. Nevertheless, there is always the risk that the calcium hydrogen carbonate formed by the reaction of released carbonic acid with calcium carbonate will decompose again into calcium carbonate and carbon dioxide in the course of the paper production process and calcium carbonate deposits will occur, which lead to production interruptions.
Eine modifizierte pseudoneutrale Papierherstellungsmethode wird in der japanischen Offenlegungsschrift 83-174 696 beschrieben. Hierbei wird dem Aluminiumsulfat als zusätzliches Mittel noch ein Dicyandiamid-Formaldehyd-Kondensationsprodukt zugesetzt. Dieses Verfahren hat jedoch immer noch den Nachteil, daß ein teueres Diketenharz verwendet werden muß.A modified pseudo-neutral paper making method is described in Japanese Patent Laid-Open No. 83-174,696. Here, a dicyandiamide-formaldehyde condensation product is added to the aluminum sulfate as an additional agent. However, this method still has the disadvantage that an expensive diketene resin has to be used.
In der europäischen Offenlegungsschrift 112 525 wird ein Mittel zur Neutralleimung von cellulosehaltigen Materialien vorgeschlagen, welches aus Wasser, einem in Wasser unbegrenzt löslichen Alkohol, Alkali- oder Aluminiumhydroxid sowie einer gesättigten oder ungesättigten Fettsäure mit 12 bis 24 C-Atomen besteht.European patent application 112 525 proposes a means for neutral sizing of cellulose-containing materials, which consists of water, a in Unlimited water soluble alcohol, alkali or aluminum hydroxide and a saturated or unsaturated fatty acid with 12 to 24 carbon atoms.
Ziel der neutralen Fahrweise der Papierherstellung ist es, den Einsatz von Aluminiumsulfat weitgehend zu reduzieren oder ganz auszuschließen und Kaolin als Füllstoff oder Pigment durch Calciumcarbonat zu ersetzen. Letzteres ist kostengünstiger erhältlich als Kaolin, und sein Weißgrad übersteigt den des Kaolins. Durch das günstigere Fließverhalten des Calciumcarbonats können außerdem höhere Füllungsgrade im Papier realisiert werden. Darüberhinaus wird die Korrosion an den maschinellen Einrichtungen verringert und die Qualität des Papiers, insbesondere dessen Alterungsbeständigkeit deutlich verbessert.The aim of the neutral paper production process is to largely reduce or eliminate the use of aluminum sulfate and to replace kaolin as filler or pigment with calcium carbonate. The latter is less expensive than kaolin and its whiteness exceeds that of kaolin. Due to the more favorable flow behavior of calcium carbonate, higher degrees of filling can also be achieved in the paper. In addition, the corrosion on the machine equipment is reduced and the quality of the paper, in particular its resistance to aging, is significantly improved.
Der vorliegenden Erfindung liegt daher die Aufgabe zugrunde, ein Papierherstellungsverfahren zu entwickeln, das bei neutralen bis schwach basischen pH-Bereichen arbeitet und unter diesen Bedingungen die Nachteile der bisher bekannten Verfahren vermeidet.The present invention is therefore based on the object of developing a paper production process which operates in neutral to weakly basic pH ranges and under these conditions avoids the disadvantages of the previously known processes.
Gelöst wird diese Aufgabe durch ein Verfahren zur Leimung bei der Herstellung von Papier, Karton, Pappen und anderen cellulosehaltigen Materialien mit und ohne Füllstoffe und/oder Pigmente durch natürliche oder synthetische Leimungsmittel unter neutralen bis schwach basischen pH-Bedingungen, welches dadurch gekennzeichnet ist, daß man mit einer Kombination von natürlichen oder synthetischen Leimungsmitteln mit einem kationischen Dicyandiamidharz leimt.This object is achieved by a process for sizing in the production of paper, cardboard, cardboard and other cellulose-containing materials with and without fillers and / or pigments by natural or synthetic sizing agents under neutral to weakly basic pH conditions, which is characterized in that one glues with a combination of natural or synthetic sizing agents with a cationic dicyandiamide resin.
Es wurde überraschenderweise gefunden, daß kationische Dicyandiamidharze in der Lage sind, unter neutralen bis schwach basischen pH-Bedingungen auch natürliche Leimungsmittel zu flocken und auf der Faser zu fixieren. Auch ohne Zugabe von Aluminiumsulfat kann daher mit Hilfe solcher Dicyandiamidharze eine Volleimung erzielt werden.It has surprisingly been found that cationic dicyandiamide resins are able to flocculate and fix natural sizing agents under neutral to weakly basic pH conditions and fix them on the fiber. Even without the addition of aluminum sulfate, full sizing can therefore be achieved with the aid of such dicyandiamide resins.
Auch bei synthetischen Leimen auf Diketenbasis kann überraschenderweise mittels kationischer Dicyandiamidharze eine Voll- oder Teilleimung erreicht werden, wobei keine weiteren Hilfsmittel oder Fixiermittel benötigt werden.Even with synthetic glues based on diketene, full or partial sizing can surprisingly be achieved using cationic dicyandiamide resins, with no further auxiliaries or fixing agents being required.
Als besonders geeignet haben sich kationische Dicyandiamidharze erwiesen, die eine hohe positive Ladung aufweisen und daher anionische höhermolekulare Stoffe schnell und praktisch quantitativ auszufällen in der Lage sind. Diese Harze werden zweckmäßigerweise nicht zu stark sauer eingestellt, damit nach dem Vermischen mit der Stoffsuspension der pH-Wert nicht wesentlich unter 7 absinkt.Cationic dicyandiamide resins which have a high positive charge and which are therefore able to precipitate anionic, high molecular weight substances quickly and practically quantitatively have proven to be particularly suitable. These resins are expediently not made too acidic, so that after mixing with the stock suspension the pH does not drop significantly below 7.
Die Herstellung der erfindungsgemäß verwendeten kationischen Dicyandiamidharze kann zum Beispiel durch Umsetzung von 1 Mol Dicyandiamid mit 1,0 bis 4,0 Mol Formaldehyd in Gegenwart von 0,1 bis 2,0 Mol wenigstens einer anorganischen oder organischen Säure und/oder wenigstens eines Ammonium- oder Aminsalzes davon und gegebenenfalls bis 0,5 Mol eines zwei- oder mehrwertigen Amins erfolgen. So hergestellte Kondensationsprodukte weisen pH-Werte von etwa 3 bis etwa 5 auf, sind in jedem Verhältnis mit Wasser mischbar und als etwa 50%ige wäßrige Lösung gut anwendbar.The cationic dicyandiamide resins used according to the invention can be prepared, for example, by reacting 1 mol of dicyandiamide with 1.0 to 4.0 mol of formaldehyde in the presence of 0.1 to 2.0 mol of at least one inorganic or organic acid and / or at least one ammonium or amine salt thereof and optionally up to 0.5 mol of a di- or polyvalent amine. Condensation products prepared in this way have pH values of about 3 to about 5, are miscible with water in any ratio and can be used well as an approximately 50% aqueous solution.
Als Säuren können z. B. starke anorganische Säuren wie Salzsäure, Schwefelsäure oder Salpetersäure eingesetzt werden. Bevorzugt werden jedoch schwächer saure organische Säuren wie z. B. Ameisensäure, Essigsäure oder Oxalsäure verwendet.As acids such. B. strong inorganic acids such as hydrochloric acid, sulfuric acid or nitric acid. However, weakly acidic organic acids such as. B. formic acid, acetic acid or oxalic acid is used.
Als Ammoniumsalz können bei der Harzherstellung z. B. Ammoniumsalze starker anorganischer Säuren wie Ammoniumchlorid oder Ammoniumsulfat oder Ammoniumsalze organischer Säuren wie Ammoniumformiat oder -acetat verwendet werden. Als Aminsalze können Salze aus organischen Aminen mit anorganischen oder organischen Sauren wie z. B. Ethylendiamin-formiat oder Triethylentetramin-Hydrochlorid verwendet werden. Die genannten Salze können auch im Gemisch mit anorganischen oder organischen Säuren eingesetzt werden.As ammonium salt can be used in resin production such. B. ammonium salts of strong inorganic acids such as ammonium chloride or ammonium sulfate or ammonium salts of organic acids such as ammonium formate or acetate can be used. As amine salts, salts of organic amines with inorganic or organic acids such as. B. ethylenediamine formate or triethylenetetramine hydrochloride can be used. The salts mentioned can also be used in a mixture with inorganic or organic acids.
Als gegebenenfalls noch zuzusetzende Aminkomponente können zwei- oder mehrwertige aliphatische Amine verwendet werden. Bevorzugt werden Ethylendiamin, Propylendiamin, Diethylentriamin und Triethylentetramin verwendet. Auch ihre am Stickstoff durch Hydroxylgruppen substituierten Derivate sind einsetzbar wie z. B. Mono- oder Diethanolamin. Falls Amine zugesetzt werden, beträgt ihre Menge vorzugsweise wenigstens 0,05 Mol je Mol Dicyandiamid.Divalent or polyvalent aliphatic amines can be used as the amine component to be added. Ethylene diamine, propylene diamine, diethylene triamine and triethylene tetramine are preferably used. Their derivatives substituted on the nitrogen by hydroxyl groups can also be used, such as, for. B. mono- or diethanolamine. If amines are added, their amount is preferably at least 0.05 mol per mol of dicyandiamide.
Formaldehyd kann in beliebiger Form, vorzugsweise in Form seiner 30 bis 40 Gew.-%igen wäßrigen Lösungen verwendet werden.Formaldehyde can be used in any form, preferably in the form of its 30 to 40% by weight aqueous solutions.
Unter neutralen bis schwach basischen pH-Werten werden hier solche zwischen pH 6,5 und 8,5, vorzugsweise zwischen 7,0 und 8,0 verstanden.Neutral to weakly basic pH values are understood to mean those between pH 6.5 and 8.5, preferably between 7.0 and 8.0.
Die nach dem beschriebenen Verfahren erhaltenen Kondensationsprodukte sind klare, farblose, in jedem Verhältnis mit Wasser mischbare Produkte.The condensation products obtained by the process described are clear, colorless, water-miscible products.
Im Rahmen der Erfindung können jedoch auch nach anderen Verfahren hergestellte kationische Dicyandiamidharze verwendet werden.However, cationic dicyandiamide resins produced by other processes can also be used within the scope of the invention.
Die aufzuwendende Menge an kationischem Dicyandiamidharz wird auf die "Stoff" (Cellulose)-Menge bezogen und beträgt im allgemeinen 0,1 bis 10 Gew.-%; bevorzugt werden 0,2 bis 5 Gew.-% Dicyandiamidharz angewandt, zweckmäßig in Form einer etwa 50%igen wäßrigen Lösung.The amount of cationic dicyandiamide resin to be used is based on the "substance" (cellulose) amount and is generally 0.1 to 10% by weight; 0.2 to 5% by weight of dicyandiamide resin is preferably used, advantageously in the form of an approximately 50% strength aqueous solution.
Bei dem erfindungsgemäßen Verfahren können alle handelsüblichen Leime auf Basis natürlicher oder synthetischer Ausgangsstoffe verwendet werden. Geeignete Produkte sind z. B. Kolophonium, Tierleim, Casein, Stärke, Wachse, Fettsäuren und Tallharze. Von synthetischen Leimen eignen sich besonders Produkte auf Basis von Ketendimeren,In the process according to the invention, all commercially available glues based on natural or synthetic starting materials can be used. Suitable products are e.g. B. rosin, animal glue, casein, starch, waxes, fatty acids and tall resins. Synthetic glues are particularly suitable for products based on ketene dimers,
Polyvinylalkoholen oder Polyvinylacetaten. Als Ketendimere finden Produkte Anwendung, die auf Basis von alkylsubstituierten, dimeren Ketenen mit Oxetanon-Struktur, ausgehend von langkettigen Fettsäuren, hergestellt worden sind und unter dem Markennamen Aquapel vertrieben werden. In gleicher Weise eignen sich auch modifizierte Harzleime, wie sie z. B. durch Umsetzung von z. B. Kolophonium mit dienophilen Säuren erhalten werden und unter der Markenbezeichnung Furtin 3 N/S im Handel sind. Darüberhinaus sind auch äußerst fein verteilte Dispersionen speziell modifizierter, verstärkter Harze (z. B. Furtin BVR 510) vorteilhaft anwendbar.Polyvinyl alcohols or polyvinyl acetates. Products used as ketene dimers are those which have been prepared on the basis of alkyl-substituted, dimeric ketene with an oxetanone structure, starting from long-chain fatty acids, and which are sold under the brand name Aquapel. In the same way, modified resin glues such as z. B. by implementing z. B. rosin can be obtained with dienophilic acids and are commercially available under the brand name Furtin 3 N / S. In addition, extremely finely divided dispersions of specially modified, reinforced resins (e.g. Furtin BVR 510) can be used with advantage.
Das erfindungsgemäße Verfahren erlaubt es nun überraschenderweise, durch Kombinationen von kationischem Dicyandiamidharz mit den vorstehend genannten, chemisch recht unterschiedlichen Leimkomponenten, diese zu flocken und auf der Faser zu fixieren. Ohne Zuhilfenahme weiterer Hilfsmittel kann auf diese Weise mit natürlichen, synthetischen oder modifizierten Harzleimen Voll- oder Teilleimung des Papieres erreicht werden.The method according to the invention now surprisingly makes it possible to flocculate and fix it on the fiber by combining cationic dicyandiamide resin with the chemically very different glue components mentioned above. In this way, full or partial sizing of the paper can be achieved with natural, synthetic or modified resin glues without the aid of further aids.
Sämtliche in der Papierherstellung üblichen Füllstoffe und Pigmente können auch beim erfindungsgemäßen Verfahren verwendet werden wie z. B. Kaolin, Aluminiumsilikate, Calciumsilikate, Oxihydrate von Aluminium, Talkum, Satinweiß, Gips, Bariumsulfat, Bariumcarbonat, Magnesit, Zinkoxid, Titandioxid. Bevorzugt wird jedoch Calciumcarbonat verwendet. Dieses kann in feingemahlener Form aus natürlichem Calciumcarbonat bestehen oder auch gefälltes Calciumcarbonat sein. Calciumcarbonat wird deshalb bevorzugt, da sein Weißgrad z. B. den des Kaolins übersteigt und sein günstiges Fließverhalten besonders hohe Füllungsgrade im Papier erreichen läßt. Damit werden auch die Papiereigenschaften positiv beeinflußt: Die Opazität wird erhöht, der Weißgrad verbessert, die Alterungsbeständigkeit erhöht und die mechanischen Eigenschaften gesteigert.All fillers and pigments customary in paper production can also be used in the process according to the invention, such as, for. B. kaolin, aluminum silicates, calcium silicates, oxyhydrates of aluminum, talc, satin white, gypsum, barium sulfate, barium carbonate, magnesite, zinc oxide, titanium dioxide. However, calcium carbonate is preferably used. This can consist of finely ground natural calcium carbonate or precipitated calcium carbonate. Calcium carbonate is preferred because its whiteness z. B. exceeds that of kaolin and its favorable flow behavior allows particularly high filling levels in the paper to be achieved. This also has a positive influence on the paper properties: opacity is increased, whiteness is improved, aging resistance is increased and mechanical properties are increased.
Die nachfolgenden Beispiele erläutern die Erfindung und zeigen insbesondere, welche unterschiedlichen Leimsorten durch kationische Dicyandiamidharze unter neutralen oder schwach basischen pH-Bedingungen auf Cellulosefasern aufgebracht werden können und welche guten Ergebnisse so erreicht werden.The following examples explain the invention and in particular show which different types of glue can be applied to cellulose fibers by cationic dicyandiamide resins under neutral or weakly basic pH conditions and which good results are achieved in this way.
Herstellung eines kationischen Dicyandiamid-Formaldehyd-Harzes: 84 Gew.-Teile Dicyandiamid werden mit 220 Gew.-Teilen 30%igen wäßrigen Formaldehyd und 43 Gew.-Teilen Ammoniumchlorid in ein mit Rückflußkühler ausgestattetes Rührgefäß vorgelegt. Bei Raumtemperatur werden sodann 7,7 Gew.-Teile Ethylendiamin (78%ig) unter Rühren zugesetzt. Die Reaktion springt sofort an und die Temperatur des Reaktionsgemisches steigt auf 90 bis 95°C. Nach etwa 10 Minuten ist die Reaktion beendet. Danach wird Wasser zugegeben, um eine Konzentration von 50 Gew.-% Feststoff im Harz einzustellen.Preparation of a cationic dicyandiamide-formaldehyde resin: 84 parts by weight of dicyandiamide are placed in a stirred vessel equipped with a reflux condenser with 220 parts by weight of 30% strength aqueous formaldehyde and 43 parts by weight of ammonium chloride. At room temperature, 7.7 parts by weight of ethylenediamine (78%) are then added with stirring. The reaction starts immediately and the temperature of the reaction mixture rises to 90 to 95 ° C. The reaction is complete after about 10 minutes. Then water is added to adjust the concentration of 50% by weight of solid in the resin.
Anstelle von Ethylendiamin kann z. B. auch die entsprechende Menge Diethylentriamin Triethylentetramin oder Diethanolamin verwendet werden.Instead of ethylenediamine z. B. also the appropriate amount of diethylenetriamine, triethylenetetramine or diethanolamine can be used.
Anstelle von Ammoniumchlorid kann eine anorganische oder organische Säure wie z. B. Salzsäure oder Ameisensäure verwendet werden.Instead of ammonium chloride, an inorganic or organic acid such as. B. hydrochloric acid or formic acid can be used.
Auf einem Rapid-Köthen Blattbildner werden unter Verwendung von gebleichtem Kiefernzellstoff eines Mahlgrades 24°SR, Harzleim (Freiharzleim Furtin 3N) und 50Xigem wäßrigem kationischem Dicyandiamidharz (hergestellt aus Dicyandiamid, Formaldehyd, Ammonchlorid und Ethylendiamin) Blätter gebildet und auf Zylindern thermisch 3 Minuten lang bei 120°C behandelt. Nach der Klimatisierung wurde die Leimung durch die Wasseraufnahme mittels des Cobb-Tests (60 sec.) nach DIN 53132 bestimmt. Der Verwendung des kationischen Dicyandiamidharzes wurde Alaun als Leimungsmittel gegenübergestellt, wobei sich der pH-Wert von selbst einstellte.Leaves are formed on a Rapid-Köthen sheet former using bleached pine pulp with a freeness of 24 ° SR, resin glue (free resin glue Furtin 3N) and 50X aqueous cationic dicyandiamide resin (made from dicyandiamide, formaldehyde, ammonium chloride and ethylenediamine) and thermally applied on cylinders for 3 minutes 120 ° C treated. After the air conditioning, the sizing was determined by the water absorption using the Cobb test (60 sec.) In accordance with DIN 53132. The use of the cationic dicyandiamide resin was compared to alum as a sizing agent, the pH adjusting itself.
Gegenüberstellung der Wirksamkeit des erfindungsgemäßen Papierherstellungsverfahrens mit kationischem Dicyandiamidharz und Alaun:
Ergebnis: Bei pH-Werten oberhalb 7 kann bei Einsatz von kationischem Dicyandiamidharz eine Voll-Leimung erzielt werden, die sich bei Verwendung von Alaun in diesem pH-Bereich nicht erreichen läßt.Result: At pH values above 7, full sizing can be achieved when using cationic dicyandiamide resin, which cannot be achieved in this pH range when using alum.
Blattbildung unter Verwendung von Calciumcarbonat als Füllstoff.Sheet formation using calcium carbonate as a filler.
Die Versuchsbedingungen waren die gleichen wie in Beispiel 1, jedoch wurde schwach anionisches Calciumcarbonat als Füllstoff zugesetzt. Das Gewichtsverhältnis von Zellstoff zu Füllstoff betrug 1:2. Der Füllstoff wurde 5 Minuten im Ultra Turrax (Dispergiergerät) aufbereitet, anschließend 3 Minuten mit dem Zellstoff vermischt und danach der Leim und das kationische Dicyandiamidharz zugegeben.
Ergebnis: Die Verwendung von kationischem Dicyandiamidharz läßt bei Einsatz von Harzleim u. Calciumcarbonat als Füllstoff ohne Zusatz von Alaun im pH-Bereich von 7,5 eine Voll-Leimung erreichen.Result: The use of cationic dicyandiamide resin allows u. Calcium carbonate as a filler can achieve full sizing without adding alum in the pH range of 7.5.
Blattbildung unter Verwendung von biketenleim und Calciumcarbonat als FüllstoffSheet formation using bikete glue and calcium carbonate as filler
Es wurde das gleiche kationische Dicyandiamidharz und die gleiche Calciumcarbonatqualität verwendet wie im Beispiel 2. Zum Leimen wurde ein synthetisches Produkt auf Diketenbasis (Aquapel 2) verwendet. Die Qualität der Leimung wurde mit dem Cobb-Test festgestellt.
Ergebnis: Bereits durch Zusatz von geringen Mengen an kationischem Dicyandiamidharz wird die Leimung stark verbessert; der pH-Wert der Stoffsuspension wird durch Zusatz dieses Harzes nicht verändert.Result: The addition of small amounts of cationic dicyandiamide resin greatly improves the sizing; the pH of the stock suspension is not changed by adding this resin.
Als Dicyandiamidharz wurde in diesem Beispiel ein 50 Gew.-% Feststoff enthaltendes Kondensationsprodukt aus Dicyandiamid, Formaldehyd und Ameisensäure verwendet, wobei das Molverhältnis der Komponenten 1 : 1,5 : 0,5 betrug. Als Leim wurde ein vollverseifter Harzleim (Furtin 3 N/S) verwendet. Von den, wie unter Beispiel 1 hergestellten Blättern, wurden die Cobb-Werte ermittelt.
Ergebnis: Bei Verwendung eines vollverseiften Harzleims und Einsatz eines kationischen Dicyandiamidharzes läßt sich bei pH-Werten über 7 ein guter Leimungseffekt erzielen.Result: When using a fully saponified resin glue and a cationic dicyandiamide resin, a good sizing effect can be achieved at pH values above 7.
Es wurde das gleiche Dicyandiamidharz und der gleiche Harzleim verwendet wie im Beispiel 4. Als Füllstoff diente schwach anionisches Calciumcarbonat. Die Blätter wurden in analoger Weise, wie unter Beispiel 1 angegeben, hergestellt.
Ergebnis: Auch bei Einsatz von anionischem Calciumcarbonat als Füllstoff und Verwendung von vollverseiftem Harzleim kann bei pH-Werten über 7 ein ausreichender Leimunaseffekt erzielt werden.Result: Even when using anionic calcium carbonate as a filler and using fully saponified resin glue, a sufficient glue effect can be achieved at pH values above 7.
Unter Verwendung des gleichen, in Beispiel 4 genannten, kationischen Dicyandiamidharzes sowie eines fein dispergierten, speziell modifizierten Harzleims (Furtin BVR 510) wurden gemäß Beispiel 1 Blätter gebildet. Deren Eigenschaften werden in nachfolgender Tabelle dargestellt.
Ergebnis: Die Kombination von kationischen Dicyandiamidharz mit einem speziell modifizierten Harzleim liefert auch bei pH-Werten ≥ 7 hervorragende Cobb-Werte.Result: The combination of cationic dicyandiamide resin with a specially modified resin glue provides excellent Cobb values even at pH values ≥ 7.
Unter Verwendung des in Beispiel 6 genannten kationischen Dicyandiamidharzes, des gleichen speziell modifizierten Harzleims und schwach anionischem Calciumcarbonat als Füllstoff wurden gemäß Beispiel 1 Blätter hergestellt, deren Cobb-Werte in der folgenden Tabelle dargestellt werden.
Ergebnis: Durch Kombination eines kationischen Dicyandiamidharzes mit einem speziell modifizierten Harzleim und Füllstoff wird auch bei pH-Werten über 7 eine Voll-Leimung erzielt.Result: By combining a cationic dicyandiamide resin with a specially modified resin glue and filler, full sizing is achieved even at pH values above 7.
Claims (8)
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AT86100189T ATE47733T1 (en) | 1985-01-08 | 1986-01-08 | PROCESS FOR INTERNAL SIZING IN THE MANUFACTURE OF PAPER, BOARD, BOARD AND OTHER CELLULOSIC MATERIALS. |
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DE3500408 | 1985-01-08 | ||
DE19853500408 DE3500408A1 (en) | 1985-01-08 | 1985-01-08 | METHOD FOR THE PRODUCTION OF PAPER, CARDBOARD, PAPERBOARDS AND OTHER MATERIALS CONTAINING CELLULOSE UNDER NEUTRAL TO LOW BASIC PH CONDITIONS |
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US (1) | US5026457A (en) |
EP (1) | EP0187666B1 (en) |
AT (1) | ATE47733T1 (en) |
CA (1) | CA1274059A (en) |
DE (2) | DE3500408A1 (en) |
DK (1) | DK2986A (en) |
FI (1) | FI81861C (en) |
NO (1) | NO165810C (en) |
Cited By (2)
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WO2007053681A1 (en) * | 2005-11-01 | 2007-05-10 | International Paper Company | A paper substrate having enhanced print density |
US7682438B2 (en) | 2005-11-01 | 2010-03-23 | International Paper Company | Paper substrate having enhanced print density |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3742764A1 (en) * | 1987-12-17 | 1989-06-29 | Sueddeutsche Kalkstickstoff | FLOCKING AND / OR FIXING AGENTS FOR PAPER SIZING |
US5755930A (en) * | 1994-02-04 | 1998-05-26 | Allied Colloids Limited | Production of filled paper and compositions for use in this |
US5846663A (en) | 1994-02-07 | 1998-12-08 | Hercules Incorporated | Method of surface sizing paper comprising surface sizing paper with 2-oxetanone ketene multimer sizing agent |
US5685815A (en) * | 1994-02-07 | 1997-11-11 | Hercules Incorporated | Process of using paper containing alkaline sizing agents with improved conversion capability |
US5725731A (en) * | 1995-05-08 | 1998-03-10 | Hercules Incorporated | 2-oxetanone sizing agents comprising saturated and unsaturated tails, paper made with the 2-oxetanone sizing agents, and use of the paper in high speed converting and reprographic operations |
US5827398A (en) * | 1996-02-13 | 1998-10-27 | Allied Colloids Limited | Production of filled paper |
WO1997041302A1 (en) * | 1996-04-29 | 1997-11-06 | Minerals Technologies Inc. | Rosin-sized paper composition and method of making |
US20060288906A1 (en) * | 2005-04-27 | 2006-12-28 | Martin Wulf | Process of preparation of specific color effect pigments |
WO2009012292A1 (en) * | 2007-07-16 | 2009-01-22 | Luzenac America, Inc. | Wax coatings, methods of making coated articles and coated articles therefrom |
CA2710804C (en) | 2007-12-26 | 2013-07-02 | International Paper Company | A paper substrate containing a wetting agent and having improved print mottle |
WO2010039996A1 (en) | 2008-10-01 | 2010-04-08 | International Paper Company | A paper substrate containing a wetting agent and having improved printability |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1070916B (en) | 1959-12-10 | |||
FR1218904A (en) * | 1958-03-26 | 1960-05-13 | Basf Ag | Process for pasting paper |
US3840486A (en) * | 1972-07-03 | 1974-10-08 | Hercules Inc | Water-soluble,thermosettable resinous compositions prepared from dicyandiamide,hcho,ammonium salt and a salt of an aminopolyamide and method for preparing the same |
DE2250995B2 (en) * | 1971-10-20 | 1980-08-07 | Hercules Powder Co. Ltd., London | Process for the production of sized paper, cardboard or sized cardboard from cellulose and glue mixture that can be used in this process |
DE3000502A1 (en) * | 1977-08-19 | 1981-07-09 | Hercules Inc., 19899 Wilmington, Del. | SIZING AGENTS AND METHOD FOR SIZING PAPER AND CARDBOARD |
EP0082373A1 (en) | 1981-12-08 | 1983-06-29 | Hercules Incorporated | Dicyandiamide-formaldehyde condensates and process for preparing the same |
JPS58174696A (en) | 1982-04-06 | 1983-10-13 | 三菱製紙株式会社 | Neutral paper |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA618976A (en) * | 1961-04-25 | Badische Anilin- And Soda-Fabrik Aktiengesellschaft | Process of sizing paper | |
CH233160A (en) * | 1942-06-23 | 1944-07-15 | Ag J R Geigy | Process for the preparation of textile auxiliaries. |
DE1034858B (en) * | 1952-03-18 | 1958-07-24 | Jacques Wolf & Co | Process for the production of a resin from dicyandiamide and formaldehyde which is stable in aqueous solution and does not gel |
DE1012282B (en) * | 1952-06-16 | 1957-07-18 | Sueddeutsche Kalkstickstoff | Means for finishing textiles, paper, leather or the like. |
DE1029561B (en) * | 1955-07-25 | 1958-05-08 | Boehme Fettchemie Gmbh | Process for the production of water-soluble, hardenable, cationic condensation products from dicyandiamide and formaldehyde |
US3016325A (en) * | 1955-11-01 | 1962-01-09 | Electro Chem Fiber Seal Corp | Process of combining water-insoluble additament with organic fibrous material |
DE1078768B (en) * | 1957-02-13 | 1960-03-31 | Basf Ag | Process for the preparation of cationic condensation products |
FR1127272A (en) * | 1957-03-28 | 1956-12-12 | Sueddeutsche Kalkstickstoff | Product for refining textiles, papers, leathers or others |
US3410649A (en) * | 1967-03-01 | 1968-11-12 | Diamond Shamrock Corp | Cationic resins which are the reaction product of formaldehyde and the reaction product of amino bases with a methylolated amine salt |
US3582461A (en) * | 1968-02-14 | 1971-06-01 | Diamond Shamrock Corp | Pitch control in pulp and papermaking processes |
US3957574A (en) * | 1971-10-20 | 1976-05-18 | Hercules Powder Company Limited | Sizing method and composition for use therein |
DE2514908C3 (en) * | 1975-04-05 | 1980-08-21 | Cassella Ag, 6000 Frankfurt | Auxiliaries for the manufacture of paper and cardboard and its use |
CH632546A5 (en) * | 1977-08-26 | 1982-10-15 | Ciba Geigy Ag | METHOD FOR PRODUCING SIZED PAPER OR CARDBOARD USING POLYELECTROLYTE AND SALTS OF EPOXYD-AMINE-POLYAMINOAMIDE IMPLEMENTATION PRODUCTS. |
JPS6028959B2 (en) * | 1977-11-22 | 1985-07-08 | ライオン・アクゾ株式会社 | Paper surface sizing method |
US4240935A (en) * | 1978-12-22 | 1980-12-23 | Hercules Incorporated | Ketene dimer paper sizing compositions |
-
1985
- 1985-01-08 DE DE19853500408 patent/DE3500408A1/en not_active Withdrawn
- 1985-12-18 NO NO855124A patent/NO165810C/en unknown
- 1985-12-31 FI FI855199A patent/FI81861C/en not_active IP Right Cessation
-
1986
- 1986-01-03 DK DK2986A patent/DK2986A/en not_active Application Discontinuation
- 1986-01-06 CA CA000499052A patent/CA1274059A/en not_active Expired - Lifetime
- 1986-01-08 DE DE8686100189T patent/DE3666709D1/en not_active Expired
- 1986-01-08 EP EP86100189A patent/EP0187666B1/en not_active Expired
- 1986-01-08 AT AT86100189T patent/ATE47733T1/en not_active IP Right Cessation
-
1989
- 1989-02-28 US US07/317,113 patent/US5026457A/en not_active Expired - Fee Related
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1070916B (en) | 1959-12-10 | |||
FR1218904A (en) * | 1958-03-26 | 1960-05-13 | Basf Ag | Process for pasting paper |
DE2250995B2 (en) * | 1971-10-20 | 1980-08-07 | Hercules Powder Co. Ltd., London | Process for the production of sized paper, cardboard or sized cardboard from cellulose and glue mixture that can be used in this process |
US3840486A (en) * | 1972-07-03 | 1974-10-08 | Hercules Inc | Water-soluble,thermosettable resinous compositions prepared from dicyandiamide,hcho,ammonium salt and a salt of an aminopolyamide and method for preparing the same |
DE3000502A1 (en) * | 1977-08-19 | 1981-07-09 | Hercules Inc., 19899 Wilmington, Del. | SIZING AGENTS AND METHOD FOR SIZING PAPER AND CARDBOARD |
EP0082373A1 (en) | 1981-12-08 | 1983-06-29 | Hercules Incorporated | Dicyandiamide-formaldehyde condensates and process for preparing the same |
JPS58174696A (en) | 1982-04-06 | 1983-10-13 | 三菱製紙株式会社 | Neutral paper |
Non-Patent Citations (4)
Title |
---|
"Ulmann's Encyclopädie der technischen Chemie", vol. 10, pages: 147 |
ABSTRACT BULLETIN OF THE INSTITUTE OF PAPER CHEMISTRY, Band 55, Nr. 5, November 1984, Seite 630, Zusammenfassung Nr. 5979, Appleton, Wisc. US; & JP-A-58 174 696 (MITSUBISHI PAPER MILLS LTD.) 13.10.1983 * |
ABSTRACTS BULLETIN OF THE INSTITUTE OF PAPER CHEMISTRY, Band 49, Nr. 1, Juli 1978, Seite 65, Zusammenfassung Nr. 376, Appleton, Wisc., US; V.V. TESLENKO et al.: "Reaction of cationic polyelectrolytes with the components of a pulp suspension" & TSELLYULOZA, BUMAGA, KARTON REF. INFORM. NO. 26: 7-8 (Oct, 1977) * |
ABSTRACTS BULLETIN OF THE INSTITUTE OF PAPER CHEMISTRY, Band 54, Nr. 6, Dezember 1983, Seite 657, Zusammenfassung Nr. 6082, Appleton, Wisc, US; M. OLIVER: "Attention to sizing can improve sheet performance" & SOUTHERN PULP PAPER 46, no. 6: 32-37 (June 1983) * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007053681A1 (en) * | 2005-11-01 | 2007-05-10 | International Paper Company | A paper substrate having enhanced print density |
US7682438B2 (en) | 2005-11-01 | 2010-03-23 | International Paper Company | Paper substrate having enhanced print density |
EP2511419A1 (en) * | 2005-11-01 | 2012-10-17 | International Paper Company | A paper substrate having enhanced print density |
US10036123B2 (en) | 2005-11-01 | 2018-07-31 | International Paper Company | Paper substrate having enhanced print density |
Also Published As
Publication number | Publication date |
---|---|
FI81861B (en) | 1990-08-31 |
NO855124L (en) | 1986-07-09 |
DK2986D0 (en) | 1986-01-03 |
DK2986A (en) | 1986-07-09 |
FI855199A0 (en) | 1985-12-31 |
NO165810B (en) | 1991-01-02 |
FI855199A (en) | 1986-07-09 |
FI81861C (en) | 1990-12-10 |
DE3500408A1 (en) | 1986-07-10 |
NO165810C (en) | 1991-04-10 |
US5026457A (en) | 1991-06-25 |
DE3666709D1 (en) | 1989-12-07 |
EP0187666B1 (en) | 1989-11-02 |
CA1274059A (en) | 1990-09-18 |
ATE47733T1 (en) | 1989-11-15 |
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