US20130126117A1 - Composition and process for whitening paper - Google Patents
Composition and process for whitening paper Download PDFInfo
- Publication number
- US20130126117A1 US20130126117A1 US13/813,160 US201113813160A US2013126117A1 US 20130126117 A1 US20130126117 A1 US 20130126117A1 US 201113813160 A US201113813160 A US 201113813160A US 2013126117 A1 US2013126117 A1 US 2013126117A1
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- composition
- paper
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- weight
- starch
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- 239000000203 mixture Substances 0.000 title claims abstract description 54
- 230000002087 whitening effect Effects 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title claims description 17
- 239000006081 fluorescent whitening agent Substances 0.000 claims abstract description 36
- 150000003839 salts Chemical class 0.000 claims abstract description 17
- 150000001768 cations Chemical class 0.000 claims abstract description 11
- 238000004381 surface treatment Methods 0.000 claims abstract description 6
- -1 hydroxypropyl Chemical group 0.000 claims description 23
- 229920002472 Starch Polymers 0.000 claims description 19
- 235000019698 starch Nutrition 0.000 claims description 18
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims description 14
- 239000008107 starch Substances 0.000 claims description 14
- 239000001110 calcium chloride Substances 0.000 claims description 12
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 12
- 238000004513 sizing Methods 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 6
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 5
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 5
- 229920002678 cellulose Polymers 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 5
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 5
- 229910052700 potassium Inorganic materials 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 4
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 description 7
- 125000000217 alkyl group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 238000007639 printing Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- RWFZHFYWPYSEOZ-UHFFFAOYSA-N 1,2-diphenyl-N,N'-bis(triazin-4-yl)ethene-1,2-diamine Chemical class N1=NN=C(C=C1)NC(=C(C1=CC=CC=C1)NC1=NN=NC=C1)C1=CC=CC=C1 RWFZHFYWPYSEOZ-UHFFFAOYSA-N 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000007641 inkjet printing Methods 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 229920001131 Pulp (paper) Polymers 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001592 potato starch Polymers 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- NJVOHKFLBKQLIZ-UHFFFAOYSA-N (2-ethenylphenyl) prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1C=C NJVOHKFLBKQLIZ-UHFFFAOYSA-N 0.000 description 1
- ZMLPKJYZRQZLDA-UHFFFAOYSA-N 1-(2-phenylethenyl)-4-[4-(2-phenylethenyl)phenyl]benzene Chemical group C=1C=CC=CC=1C=CC(C=C1)=CC=C1C(C=C1)=CC=C1C=CC1=CC=CC=C1 ZMLPKJYZRQZLDA-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- REJHVSOVQBJEBF-OWOJBTEDSA-N 5-azaniumyl-2-[(e)-2-(4-azaniumyl-2-sulfonatophenyl)ethenyl]benzenesulfonate Chemical compound OS(=O)(=O)C1=CC(N)=CC=C1\C=C\C1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-OWOJBTEDSA-N 0.000 description 1
- 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 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- REJHVSOVQBJEBF-UHFFFAOYSA-N DSD-acid Natural products OS(=O)(=O)C1=CC(N)=CC=C1C=CC1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-UHFFFAOYSA-N 0.000 description 1
- 229920001612 Hydroxyethyl starch Polymers 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 235000019759 Maize starch Nutrition 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 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 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001212 derivatisation Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical group OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043276 diisopropanolamine Drugs 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229940050526 hydroxyethylstarch Drugs 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 230000000670 limiting effect Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229940116317 potato starch Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 229940100486 rice starch Drugs 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 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 1
- 229940100445 wheat starch Drugs 0.000 description 1
Images
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
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/30—Luminescent or fluorescent substances, e.g. for optical bleaching
-
- 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
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/07—Nitrogen-containing compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/09—Sulfur-containing compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—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
- D21H17/51—Triazines, e.g. melamine
Definitions
- the present invention relates to a composition suitable for surface treatment of paper, in particular a size press liquor, and a process for whitening paper using said composition.
- a sizing step is usually carried out for achieving good writing and printing properties and strength.
- Such a sizing step can take place, on the one hand, before the sheet formation in the paper pulp (internal sizing) and, on the other hand, after the sheet formation in the size press.
- a combination of both processes is also possible.
- whitening of the pulp or of the paper sheet is usually also carried out by means of a fluorescent whitening agent (FWA).
- FWA fluorescent whitening agent
- the size and fluorescent whitening agent are added separately to the paper pulp in the case of pulp application, whereas the fluorescent whitening agent is incorporated into the size press liquor and applied together with it to the paper sheet in the case of surface sizing.
- WO 2009/150180 A1 and EP 2 135 997 A1 disclose aqueous compositions containing specific bis-triazinylamino-stilbene compounds containing alkylsulfonic acid groups, a salt of a bivalent cation, and a carrier.
- the FIGURE is a diagram showing the influence of calcium chloride on the performance of different fluorescent whitening agents according to present disclosure.
- the present invention relates to a composition suitable for surface treatment of paper, wherein the composition contains
- n and m are, independently of each other, an integer of 1, 2, or 3;
- R 1 , R 2 , R 3 , and R 4 represent, independently of each other, hydrogen, C 1 -C 4 alkyl, C 2 -C 4 alkoxyalkyl, C 2 -C 4 cyanoalkyl, or C 2 -C 4 hydroxyalkyl; or R 1 and R 2 or R 3 and R 4 independently of each other together with N atom form morpholine, piperidine or pyrrolidine ring;
- R 1 , R 2 , R 3 and R 4 contains at least 3 carbon atoms
- M represents hydrogen, or one equivalent of a cation, in particular Li, Na, K, Ca, Mg, ammonium, or ammonium which is mono-, di-, tri- or tetra-substituted by C 1 -C 4 alkyl or C 2 -C 4 hydroxyalkyl;
- the invention further relates to a process for whitening paper, wherein a cellulose sheet is brought into contact with the above defined composition, preferably in the size press.
- a process for whitening paper wherein a cellulose sheet is brought into contact with the above defined composition, preferably in the size press.
- the composition suitable for surface treatment of paper is a size press liquor
- the process is a process for whitening paper in the size press, wherein a cellulose sheet is brought into contact with the size press liquor.
- size press is understood as meaning a surface application unit, preferably of the paper machine, in which the cellulose sheet formed is brought into contact with a size press liquor, and in which the proportion of the liquor which is to be taken up by the sheet (liquor absorption) can preferably be adjusted by means of the roll pressure.
- the composition contains at least one bis-triazinylamino-stilbene compound of the above defined formula (I), wherein n, m, R 1 to R 4 , and M are as defined above.
- the alkyl group can be linear or branched, and the possible substituents of the alkyl group, which are alkoxy, hydroxyl and/or cyano groups, can be attached at any position of the alkyl chain.
- C 2 -C 4 alkoxyalkyl means C 2 -C 4 alkyl substituted with C 2 -C 4 alkoxy.
- n and m are integers from 1 to 2, most preferred 2.
- R 1 , R 2 , R 3 and R 4 represent, independently of each other, hydrogen, C 1 -C 4 alkyl, C 2 -C 4 cyanoalkyl, or C 2 -C 4 hydroxyalkyl, in particular propyl, cyanoethyl, or hydroxypropyl.
- the —SO 3 M groups at the terminal aromatic rings can be in o-, m-, or p-position. The preferred positions depend on the number of the —SO 3 M groups. If n or m is 1, p-position is preferred. If n or m is 2, the 2,5-position is preferred.
- R 1 , R 2 , R 3 and R 4 is propyl, cyano-ethyl or hydroxypropyl.
- R 1 , R 2 , R 3 and R 4 are propyl or hydroxypropyl, in particular all are either propyl or hydroxypropyl, wherein preferably n and m are 2.
- the hydroxypropyl group is a hydroxyisopropyl group.
- n and m are 2, and the two —SO 3 M groups are in 2,5-position.
- n and m are 2, R 1 and R 3 are hydroxyisopropyl, and R 2 and R 4 are cyanoethyl.
- At least one of R 1 , R 2 , R 3 and R 4 contains at least 3 carbon atoms.
- at least one of R 1 and R 2 and at least one of R 3 and R 4 contain at least 3 carbon atoms.
- at least one of R 1 , R 2 , R 3 and R 4 in particular at least one of R 1 and R 2 and at least one of R 3 and R 4 , represent(s) C 3 -C 4 alkyl, C 3 -C 4 alkoxyalkyl, C 3 -C 4 cyanoalkyl, or C 3 -C 4 hydroxyalkyl.
- C 3 -C 4 alkoxyalkyl means C 3 or C 4 alkyl substituted with C 3 or C 4 alkoxy.
- M are hydrogen, Na, K, Ca, Mg, in particular M is Na or K, most preferred is Na.
- the fluorescent whitening agents of formula (I) can be produced by known procedures, and are used as free acids or as salts thereof, preferably alkali metal salts.
- the compounds are prepared by reacting cyanuric chloride with 4,4′-diaminostilbene-2,2′-disulfonic acid or a salt thereof, and an appropriate aniline derivative containing a phenyl ring substituted with —SO 3 M group(s), and substituted aliphatic amines or heterocyclic compounds.
- EP 0 860 437 A1 describes the preparation of such compounds.
- composition of the invention can contain more than one, preferably two or three, most preferred three, of the fluorescent whitening agents of formula (I).
- Component (a) of the composition can contain, in addition to the at least one fluorescent whitening agent of formula (I), one or more known bis-triazinylamino-stilbene or distyryl-biphenyl based fluorescent whitening agents.
- the salt of component (b) of the composition of the invention comprises bivalent cations, preferably cations of an earth alkaline metal, in particular calcium or magnesium.
- the counterions of the bivalent cations are mono- or multivalent anions, in particular halide, sulphate, hydrosulphate, phosphate, hydrophosphate, dihydrophosphate, carbonate, hydrocarbonate, nitrate, acetate, or a mixture thereof, preferably chloride or sulphate, most preferably chloride.
- the salts disclosed in U.S. Pat. No. 6,207,258 B1 are also suitable.
- a preferred salt is calcium chloride, magnesium chloride, magnesium sulphate, or a mixture thereof; more preferred is calcium chloride, magnesium chloride, or a mixture thereof; most preferred is calcium chloride.
- the carrier of component (c) is any compound known in the art to be suitable as a carrier, in particular carriers suitable for size press liquors.
- Preferred carriers are carboxymethylcellulose (CMC), polyvinyl alcohol (PVA), starch or mixtures thereof, with starch being particularly preferred.
- Suitable carrier substances are, for example, hydrophilic polymers having the ability to form hydrogen bridge bonds.
- Preferred carrier substances are starch, polyvinyl alcohols, carboxymethylcelluloses and polyethylene glycols having a number average molecular weight of from 200 to 8000 g/mol, as well as any desired mixtures of these substances, it being possible for these polymers optionally to be modified.
- Preferred polyvinyl alcohols are those having a degree of hydrolysis >85%, preferred carboxymethylcelluloses are those having a degree of substitution DS of >0.5.
- Polyethylene glycols having a number average molecular weight Mn of from 200 to 8000 g/mol are particularly preferred.
- Suitable starches are based e.g., but not exclusively, on potato starch, rice starch, wheat starch, maize starch or tapioca starch. In particular, starches whose molecular weights have already been reduced by partial degradation and/or which have been obtained by derivatization are preferably used instead of natural starches. Furthermore, starches for which both modification steps have been combined, i.e. which have been partially degraded and additionally derivatized, are suitable. Typical methods for starch degradation are, for example, enzymatic, oxidative, thermal or hydrolytic treatment. Examples of suitable starch derivatives are hydroxyethyl starch or cationic starch.
- composition of the invention contains as component (d) water and, optionally, can contain sizing agents, such as alkenyl ketene dimer, alkyl ketene dimer (AKD), alkenyl succinic anhydride (ASA), rosin size, styrene maleic anhydride copolymers, styrene acrylate, styrene acrylic acid copolymers, polyurethane or ethylene acrylic acid copolymers, or other common paper chemicals, such as styryl-acrylate copolymers, latex, pigments, defoamers, or salts, such as NaCl or NaHCO 3 , or mixtures of two or more thereof.
- sizing agents such as alkenyl ketene dimer, alkyl ketene dimer (AKD), alkenyl succinic anhydride (ASA), rosin size, styrene maleic anhydride copolymers, styrene acrylate,
- the composition of the invention contains preferably component (a) in an amount of 0.02 to 3, more preferably 0.05 to 2, most preferably 0.1 to 1, weight-% based on 100 weight-% of the composition. If fluorescent whitening agents other than those of formula (I) are used, their amount is 5 to 95 weight-% based on 100 weight-% of component (a).
- Component (b) is preferably contained in an amount of 0.2 to 8, in particular 0.5 to 6, most preferably 1 to 5, weight-% based on 100 weight-% of the composition.
- Component (c) is preferably contained in an amount of 3 to 20, in particular 5 to 15, most preferably 6 to 12, weight-% based on 100 weight-% of the composition.
- the composition of the invention contains preferably water in an amount of 75 to 96.78, in particular 79 to 94.45, most preferably 82.5 to 92.9, weight-% based on 100 weight-% of the composition.
- the composition contains a sizing agent, preferably in an amount of 0 to 5, in particular 0 to 4, most preferably 0 to 3, in each case weight-% based on 100 weight-% of the composition.
- auxiliaries such as, for example, dispersants, thickeners, antifreezes, preservatives, complexing agents, etc., or organic byproducts from the fluorescent whitening agent synthesis which were not completely removed in the working-up, may be contained in the composition of the invention.
- compositions are also described in U.S. Pat. No. 6,207,258 B1, wherein according to the invention as component (a) at least one fluorescent whitening agent of formula (I) is used.
- the production of the composition is effected by known methods and preferably effected by combining an aqueous solution of the fluorescent whitening agent used as component (a), which preferably has a suitable pH value, with the other components, such as carrier substances, sizing agents, binders, pigments, salts or standardizing agents.
- component (a) which preferably has a suitable pH value
- component (c) an aqueous preparation of carrier component (c) is prepared, to which preparation an aqueous preparation of salt component (b) is added, followed by the addition of an aqueous preparation of the fluorescent whitening agent component (a), preferably adjusted in pH value, and the other components.
- composition of the invention can be used for whitening paper, in particular for surface treatment of paper, e.g. in a size press.
- the process of the invention for whitening paper is carried out according to known processes, preferably using a size press, and is subject to no restrictions.
- the paper used is not critical and may be any cellulose sheet.
- Paper obtained by the process of the invention exhibits, in addition to improved printing performance, improved whiteness, and is in particular suitable for inkjet printing applications.
- the whiteness of the papers produced can be characterized by the CIE whiteness.
- Different fluorescent whitening agents can be compared to each other with respect to the saturation behavior when determined according to CIE whiteness. In other words, if a larger amount of fluorescent whitening agent is used and no further increase in whiteness is found, there is a saturation behavior and there may even be adverse effects on the whiteness when using higher amounts.
- the effect of saturation is also referred to as greening.
- the greening limit i.e. the point at which increasing amounts of fluorescent whitening agent used results in virtually no further increase in whiteness, can be derived, for example, from the a*-b* diagram, where a* and b* are the color coordinates in the CIE-L*a*b system.
- a 15% starch solution of neutral oxidatively degraded potato starch (Perfectamyl 4692) and a 50% calcium chloride solution were prepared.
- the fluorescent whitening agent was weighed in a glass, and 13.33 g of 15% starch solution was added. Then, 50% calcium chloride solution was weighed in, and the solution was filled up with water to 20 g, so that the tests were carried out in a 10% starch solution. After stirring for a short time the solution was applied on one side of the basepaper by a semiautomatic lab coater with a Rakel (No. 2) which should simulate a film press application. 1.7 g/m 2 of dry starch was applied on that basepaper. After the drawing the paper was directly dried on a drying cylinder at about 100° C. After climatization over night the prepared side of the papers were measured with a Datacolor spectrometer (IS02469) by determining CIE, L*, a* and b*, the light source used based on ISO2469 standard.
- a Datacolor spectrometer IS02469
- the amounts used of fluorescent whitening agent per 100 g starch preparation were as indicated in Table 1 below.
- the amount of calcium chloride was 2 g for each fluorescent whitening agent.
- the following fluorescent whitening agents were used:
- the results of Table 1 are also shown in FIG. 1 .
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Abstract
The invention relates to a composition suitable for surface treatment of paper, wherein the composition contains a specified fluorescent whitening agent with a combination of specific terminal groups, a salt of a bivalent cation, and a carrier. The composition is used for whitening paper, in particular in the size press.
Description
- The present invention relates to a composition suitable for surface treatment of paper, in particular a size press liquor, and a process for whitening paper using said composition.
- In the production of paper, a sizing step is usually carried out for achieving good writing and printing properties and strength. Such a sizing step can take place, on the one hand, before the sheet formation in the paper pulp (internal sizing) and, on the other hand, after the sheet formation in the size press. A combination of both processes is also possible. In one or both production stages of paper, whitening of the pulp or of the paper sheet is usually also carried out by means of a fluorescent whitening agent (FWA). Usually, the size and fluorescent whitening agent are added separately to the paper pulp in the case of pulp application, whereas the fluorescent whitening agent is incorporated into the size press liquor and applied together with it to the paper sheet in the case of surface sizing.
- The combination of surface sizing and whitening of papers is widely used in the paper-producing industry. This method is widely used particularly in the printing and writing paper segment (copy, inkjet, offset, etc.). There is a continuing trend towards surface-sized papers having high whiteness and improved printing performance and consequently there is a demand for size press liquors which are as effective as possible. U.S. Pat. No. 6,207,258 B1 discloses a composition and process for improved inkjet printing performance using a salt of a bivalent metal, in particular calcium chloride. Therefore, in order to achieve more brilliant and sharper printings, especially inkjet printings, the paper production industry uses nowadays calcium chloride in size press liquors. However, the use of that salt affects adversely the performance of the fluorescent whitening agents commonly used in size press liquors. In particular, the whitening effectiveness is decreased, the shade is moving to the greenish-yellowish direction, and additionally a loss of fluorescence is observed.
- WO 2009/150180 A1 and
EP 2 135 997 A1 disclose aqueous compositions containing specific bis-triazinylamino-stilbene compounds containing alkylsulfonic acid groups, a salt of a bivalent cation, and a carrier. - Surprisingly, it has been found that further specific bis-triazinylamino-stilbene compounds when used in combination with salts of bivalent cations, such as calcium chloride, in compositions suitable for surface treating of paper, such as size press liquors, also overcome problems of the prior art.
- The FIGURE is a diagram showing the influence of calcium chloride on the performance of different fluorescent whitening agents according to present disclosure.
- Therefore, the present invention relates to a composition suitable for surface treatment of paper, wherein the composition contains
- (a) at least one fluorescent whitening agent of formula (I)
- wherein n and m are, independently of each other, an integer of 1, 2, or 3;
- R1, R2, R3, and R4 represent, independently of each other, hydrogen, C1-C4 alkyl, C2-C4 alkoxyalkyl, C2-C4 cyanoalkyl, or C2-C4 hydroxyalkyl; or R1 and R2 or R3 and R4 independently of each other together with N atom form morpholine, piperidine or pyrrolidine ring;
- wherein at least one of R1, R2, R3 and R4 contains at least 3 carbon atoms;
- M represents hydrogen, or one equivalent of a cation, in particular Li, Na, K, Ca, Mg, ammonium, or ammonium which is mono-, di-, tri- or tetra-substituted by C1-C4 alkyl or C2-C4 hydroxyalkyl;
- (b) at least one salt of a bivalent cation;
- (c) at least one carrier; and(d) water.
- The invention further relates to a process for whitening paper, wherein a cellulose sheet is brought into contact with the above defined composition, preferably in the size press. Preferred embodiments of the invention are described in the description hereinafter, the claims and the FIGURE.
- In a preferred embodiment of the invention, the composition suitable for surface treatment of paper is a size press liquor, and the process is a process for whitening paper in the size press, wherein a cellulose sheet is brought into contact with the size press liquor.
- In the context of this invention, size press is understood as meaning a surface application unit, preferably of the paper machine, in which the cellulose sheet formed is brought into contact with a size press liquor, and in which the proportion of the liquor which is to be taken up by the sheet (liquor absorption) can preferably be adjusted by means of the roll pressure.
- Recent developments of the size press or film press, namely of the Speedsizer as well as of the Symsizer as well as Gate-roll, are likewise understood as being covered by the term size press.
- According to the invention the composition contains at least one bis-triazinylamino-stilbene compound of the above defined formula (I), wherein n, m, R1 to R4, and M are as defined above. In the context of this invention, in the formula (I) the alkyl group can be linear or branched, and the possible substituents of the alkyl group, which are alkoxy, hydroxyl and/or cyano groups, can be attached at any position of the alkyl chain. In the present invention, C2-C4 alkoxyalkyl means C2-C4 alkyl substituted with C2-C4 alkoxy. In a preferred embodiment, n and m are integers from 1 to 2, most preferred 2. In another preferred embodiment, R1, R2, R3 and R4 represent, independently of each other, hydrogen, C1-C4 alkyl, C2-C4 cyanoalkyl, or C2-C4 hydroxyalkyl, in particular propyl, cyanoethyl, or hydroxypropyl. The —SO3M groups at the terminal aromatic rings can be in o-, m-, or p-position. The preferred positions depend on the number of the —SO3M groups. If n or m is 1, p-position is preferred. If n or m is 2, the 2,5-position is preferred. In a preferred embodiment, at least one of R1, R2, R3 and R4 is propyl, cyano-ethyl or hydroxypropyl. In another preferred embodiment, R1, R2, R3 and R4 are propyl or hydroxypropyl, in particular all are either propyl or hydroxypropyl, wherein preferably n and m are 2. Most preferably, the hydroxypropyl group is a hydroxyisopropyl group. In another preferred embodiment, n and m are 2, and the two —SO3M groups are in 2,5-position. In a further preferred embodiment, n and m are 2, R1 and R3 are hydroxyisopropyl, and R2 and R4 are cyanoethyl.
- In the compound of formula (I), at least one of R1, R2, R3 and R4 contains at least 3 carbon atoms. Preferably, at least one of R1 and R2 and at least one of R3 and R4 contain at least 3 carbon atoms. In a further preferred embodiment, at least one of R1, R2, R3 and R4, in particular at least one of R1 and R2 and at least one of R3 and R4, represent(s) C3-C4 alkyl, C3-C4 alkoxyalkyl, C3-C4 cyanoalkyl, or C3-C4 hydroxyalkyl. In the present invention, C3-C4 alkoxyalkyl means C3 or C4 alkyl substituted with C3 or C4 alkoxy.
- Preferred embodiments of M are hydrogen, Na, K, Ca, Mg, in particular M is Na or K, most preferred is Na.
- The fluorescent whitening agents of formula (I) can be produced by known procedures, and are used as free acids or as salts thereof, preferably alkali metal salts. Generally, the compounds are prepared by reacting cyanuric chloride with 4,4′-diaminostilbene-2,2′-disulfonic acid or a salt thereof, and an appropriate aniline derivative containing a phenyl ring substituted with —SO3M group(s), and substituted aliphatic amines or heterocyclic compounds. For example, EP 0 860 437 A1 describes the preparation of such compounds.
- The composition of the invention can contain more than one, preferably two or three, most preferred three, of the fluorescent whitening agents of formula (I).
- Component (a) of the composition can contain, in addition to the at least one fluorescent whitening agent of formula (I), one or more known bis-triazinylamino-stilbene or distyryl-biphenyl based fluorescent whitening agents.
- The salt of component (b) of the composition of the invention comprises bivalent cations, preferably cations of an earth alkaline metal, in particular calcium or magnesium. Preferably, the counterions of the bivalent cations are mono- or multivalent anions, in particular halide, sulphate, hydrosulphate, phosphate, hydrophosphate, dihydrophosphate, carbonate, hydrocarbonate, nitrate, acetate, or a mixture thereof, preferably chloride or sulphate, most preferably chloride. The salts disclosed in U.S. Pat. No. 6,207,258 B1 are also suitable. A preferred salt is calcium chloride, magnesium chloride, magnesium sulphate, or a mixture thereof; more preferred is calcium chloride, magnesium chloride, or a mixture thereof; most preferred is calcium chloride.
- The carrier of component (c) is any compound known in the art to be suitable as a carrier, in particular carriers suitable for size press liquors. Preferred carriers are carboxymethylcellulose (CMC), polyvinyl alcohol (PVA), starch or mixtures thereof, with starch being particularly preferred. Suitable carrier substances are, for example, hydrophilic polymers having the ability to form hydrogen bridge bonds. Preferred carrier substances are starch, polyvinyl alcohols, carboxymethylcelluloses and polyethylene glycols having a number average molecular weight of from 200 to 8000 g/mol, as well as any desired mixtures of these substances, it being possible for these polymers optionally to be modified. Preferred polyvinyl alcohols are those having a degree of hydrolysis >85%, preferred carboxymethylcelluloses are those having a degree of substitution DS of >0.5. Polyethylene glycols having a number average molecular weight Mn of from 200 to 8000 g/mol are particularly preferred. Suitable starches are based e.g., but not exclusively, on potato starch, rice starch, wheat starch, maize starch or tapioca starch. In particular, starches whose molecular weights have already been reduced by partial degradation and/or which have been obtained by derivatization are preferably used instead of natural starches. Furthermore, starches for which both modification steps have been combined, i.e. which have been partially degraded and additionally derivatized, are suitable. Typical methods for starch degradation are, for example, enzymatic, oxidative, thermal or hydrolytic treatment. Examples of suitable starch derivatives are hydroxyethyl starch or cationic starch.
- The composition of the invention contains as component (d) water and, optionally, can contain sizing agents, such as alkenyl ketene dimer, alkyl ketene dimer (AKD), alkenyl succinic anhydride (ASA), rosin size, styrene maleic anhydride copolymers, styrene acrylate, styrene acrylic acid copolymers, polyurethane or ethylene acrylic acid copolymers, or other common paper chemicals, such as styryl-acrylate copolymers, latex, pigments, defoamers, or salts, such as NaCl or NaHCO3, or mixtures of two or more thereof.
- The composition of the invention contains preferably component (a) in an amount of 0.02 to 3, more preferably 0.05 to 2, most preferably 0.1 to 1, weight-% based on 100 weight-% of the composition. If fluorescent whitening agents other than those of formula (I) are used, their amount is 5 to 95 weight-% based on 100 weight-% of component (a). Component (b) is preferably contained in an amount of 0.2 to 8, in particular 0.5 to 6, most preferably 1 to 5, weight-% based on 100 weight-% of the composition. Component (c) is preferably contained in an amount of 3 to 20, in particular 5 to 15, most preferably 6 to 12, weight-% based on 100 weight-% of the composition. The composition of the invention contains preferably water in an amount of 75 to 96.78, in particular 79 to 94.45, most preferably 82.5 to 92.9, weight-% based on 100 weight-% of the composition.
- Optionally, the composition contains a sizing agent, preferably in an amount of 0 to 5, in particular 0 to 4, most preferably 0 to 3, in each case weight-% based on 100 weight-% of the composition.
- In addition, relatively small amounts, usually amounts of less than 5% by weight, of further auxiliaries, such as, for example, dispersants, thickeners, antifreezes, preservatives, complexing agents, etc., or organic byproducts from the fluorescent whitening agent synthesis which were not completely removed in the working-up, may be contained in the composition of the invention.
- Suitable compositions are also described in U.S. Pat. No. 6,207,258 B1, wherein according to the invention as component (a) at least one fluorescent whitening agent of formula (I) is used.
- The production of the composition is effected by known methods and preferably effected by combining an aqueous solution of the fluorescent whitening agent used as component (a), which preferably has a suitable pH value, with the other components, such as carrier substances, sizing agents, binders, pigments, salts or standardizing agents. Preferably, an aqueous preparation of carrier component (c) is prepared, to which preparation an aqueous preparation of salt component (b) is added, followed by the addition of an aqueous preparation of the fluorescent whitening agent component (a), preferably adjusted in pH value, and the other components.
- The composition of the invention can be used for whitening paper, in particular for surface treatment of paper, e.g. in a size press.
- The process of the invention for whitening paper is carried out according to known processes, preferably using a size press, and is subject to no restrictions. The paper used is not critical and may be any cellulose sheet.
- Paper obtained by the process of the invention exhibits, in addition to improved printing performance, improved whiteness, and is in particular suitable for inkjet printing applications.
- The whiteness of the papers produced can be characterized by the CIE whiteness. Different fluorescent whitening agents can be compared to each other with respect to the saturation behavior when determined according to CIE whiteness. In other words, if a larger amount of fluorescent whitening agent is used and no further increase in whiteness is found, there is a saturation behavior and there may even be adverse effects on the whiteness when using higher amounts. The effect of saturation is also referred to as greening. The greening limit, i.e. the point at which increasing amounts of fluorescent whitening agent used results in virtually no further increase in whiteness, can be derived, for example, from the a*-b* diagram, where a* and b* are the color coordinates in the CIE-L*a*b system.
- The following example illustrates the invention and shows preferred embodiments, without limiting the scope of protection.
- The whitening performance of different fluorescent whitening agents in the presence of calcium chloride was studied using the following test procedure for size press application.
- First, a 15% starch solution of neutral oxidatively degraded potato starch (Perfectamyl 4692) and a 50% calcium chloride solution were prepared. The paper used was a 80 g/m2 basepaper, which was a machine paper, internally sized (Cobb equals to 110 g/m2) and slightly whitened with fluorescent whitening agent to have the following optical characteristics: CIE −104.89; L*=93.92; a*=1.21; b*=−4.34.
- The fluorescent whitening agent was weighed in a glass, and 13.33 g of 15% starch solution was added. Then, 50% calcium chloride solution was weighed in, and the solution was filled up with water to 20 g, so that the tests were carried out in a 10% starch solution. After stirring for a short time the solution was applied on one side of the basepaper by a semiautomatic lab coater with a Rakel (No. 2) which should simulate a film press application. 1.7 g/m2 of dry starch was applied on that basepaper. After the drawing the paper was directly dried on a drying cylinder at about 100° C. After climatization over night the prepared side of the papers were measured with a Datacolor spectrometer (IS02469) by determining CIE, L*, a* and b*, the light source used based on ISO2469 standard.
- The amounts used of fluorescent whitening agent per 100 g starch preparation were as indicated in Table 1 below. The amount of calcium chloride was 2 g for each fluorescent whitening agent. The following fluorescent whitening agents were used:
- The results obtained are summarized in Table 1.
-
TABLE 1 Amount (wt %) CIE FWA in starch preparation whiteness L* a* b* FWA 10.8 127.41 93.92 2.14 −9.32 1.6 133.13 94.13 2.15 −10.50 2.4 135.06 94.27 1.98 −10.87 FWA 20.8 125.94 93.87 2.11 −9.01 1.6 131.64 94.03 2.20 −10.21 2.4 133.86 94.17 2.11 −10.65 Comparative 0.8 126.13 93.98 1.80 −9.01 FWA 1.6 129.95 94.19 1.54 −9.76 2.4 130.81 94.37 1.22 −9.87 - As may be taken from Table 1,
FWA 1 andFWA 2 containing certain aliphatic amine groups, namely of diisopropanolamine or dipropylamine, in combination with dimethanilic acid, showed for almost all concentrations of fluorescent whitening agent used an improvement in whiteness in the presence of calcium chloride compared to the comparative FWA which does not contain that specific combination of groups. For further illustration, the results of Table 1 are also shown inFIG. 1 . - The above experimental data show that the use of bis-triazinylamino-stilbene fluorescent whitening agent compounds with a specific combination of terminal groups according to the invention results in paper of improved whiteness in the presence of a salt of a bivalent cation, such as calcium chloride
- This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to make and use the invention. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims.
Claims (15)
1. A composition suitable for surface treatment of paper, wherein the composition comprises
(a) at least one fluorescent whitening agent of the formula (I)
wherein n and m are, independently of each other, an integer of 1, 2, or 3;
R1, R2, R3 and R4 represent, independently of each other, hydrogen, C1-C4 alkyl, C2-C4 alkoxyalkyl, C2-C4 cyanoalkyl, or C2-C4 hydroxyalkyl; or R1 and R2 or R3 and R4 independently of each other together with N atom form morpholine, piperidine or pyrrolidine ring;
wherein at least one of R1, R2, R3 and R4 contains at least 3 carbon atoms;
M represents hydrogen, or one equivalent of a cation, in particular Li, Na, K, Ca, Mg, ammonium, or ammonium which is mono-, di-, tri- or tetra-substituted by C1-C4 alkyl or C2-C4 hydroxyalkyl;
(b) at least one salt of a bivalent cation;
(c) at least one carrier; and
(d) water.
2. The composition of claim 1 , wherein n and m each are 2, and the —SO3M groups are in 2,5-position.
3. The composition of claim 1 wherein R1, R2, R3 and R4 are, independently of each other, propyl, cyanoethyl, or hydroxypropyl.
4. The composition of claim 1 , wherein n and m are 2, and R1, R2, R3 and R4 are propyl.
5. The composition of claim 1 , wherein n and m are 2, and R1, R2, R3 and R4 are hydroxypropyl, in particular hydroxyisopropyl.
6. The composition of claim 1 , wherein n and m are 2, R1 and R3 are hydroxypropyl, in particular hydroxyisopropyl, and R2 and R4 are cyanoethyl.
7. The composition of claim 1 , wherein M is Na or K.
8. The composition of claim 1 , wherein the salt of component (b) is calcium chloride.
9. The composition of claim 1 , wherein the carrier of component (c) is selected from carboxymethylcellulose, polyvinyl alcohol, starch, and mixtures thereof.
10. The composition of claim 9 , wherein the carrier is starch.
11. The composition of claim 1 , wherein the composition contains component (a) in an amount of 0.02 to 3 weight-%, component (b) in an amount of 0.2 to 8 weight-%, and component (c) in an amount of 3 to 20 weight-%, each based on 100 weight-% of the composition.
12. The composition of claim 1 , wherein the composition is a size press liquor which optionally contains a sizing agent.
13. A process for whitening paper comprising contacting a cellulose sheet with the composition of claim 1 .
14. The process of claim 13 , wherein the contacting is conducted in a size press.
15. A paper obtainable by the process according to claim 13 .
Applications Claiming Priority (3)
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EP10171451.7 | 2010-07-30 | ||
EP10171451.7A EP2412870B1 (en) | 2010-07-30 | 2010-07-30 | Composition and process for whitening paper |
PCT/EP2011/062081 WO2012013513A1 (en) | 2010-07-30 | 2011-07-14 | Composition and process for whitening paper |
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US13/813,160 Abandoned US20130126117A1 (en) | 2010-07-30 | 2011-07-14 | Composition and process for whitening paper |
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US (1) | US20130126117A1 (en) |
EP (1) | EP2412870B1 (en) |
BR (1) | BR112013002342A2 (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160060814A1 (en) * | 2013-04-29 | 2016-03-03 | Blankophor Gmbh & Co., Kg | Use of Micronized Cellulose and Fluorescent Whitening Agent for Surface Treatment of Cellulosic Materials |
US20160177098A1 (en) * | 2013-03-21 | 2016-06-23 | Archroma Ip Gmbh | Optical brightening agents for high quality ink-jet printing |
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CN104312197B (en) * | 2014-09-05 | 2016-09-21 | 旭泰(太仓)精细化工有限公司 | A kind of hexa-sulphonic acid liquid fluorescent whitening agents and preparation method and application |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4670183A (en) * | 1983-11-15 | 1987-06-02 | The Dow Chemical Company | Method and compositions relating to the activation of fluorescent whitening agents |
US4717502A (en) * | 1985-01-23 | 1988-01-05 | Sandoz Ltd. | Aqueous optical brightener compositions |
US6025490A (en) * | 1997-02-18 | 2000-02-15 | Bayer Aktiengesellschaft | Process for the preparation of substituted 4,4'-diaminostilbene-2,2'-disulphonic acids |
US6165973A (en) * | 1999-02-05 | 2000-12-26 | Ciba Specialty Chemicals Corporation | Fluorescent whitening agent, its preparation and use |
US6365737B1 (en) * | 1998-02-20 | 2002-04-02 | Ciba Specialty Chemical Corporation | Process for the preparation of stilbene compounds |
US20030089888A1 (en) * | 2001-10-05 | 2003-05-15 | Erwin Bacher | Use of aqueous brightener preparations for brightening natural and synthetic materials |
US7258815B2 (en) * | 2002-04-19 | 2007-08-21 | Karl-Heinz Drenker | Use of brighteners for the preparation of coating slips |
US7682438B2 (en) * | 2005-11-01 | 2010-03-23 | International Paper Company | Paper substrate having enhanced print density |
US20100129553A1 (en) * | 2008-11-27 | 2010-05-27 | International Paper Company | Optical Brightening Compositions For High Quality Inkjet Printing |
US7731820B2 (en) * | 2004-10-27 | 2010-06-08 | Ciba Specialty Chemicals Corporation | Compositions of fluorescent whitening agents |
US20110126996A1 (en) * | 2008-06-11 | 2011-06-02 | Blankophor Gmbh & Co. Kg | Composition and process for whitening paper |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY125712A (en) | 1997-07-31 | 2006-08-30 | Hercules Inc | Composition and method for improved ink jet printing performance |
US7270771B2 (en) * | 2002-07-05 | 2007-09-18 | Ciba Specialty Chemicals Corporation | Triazinylaminostilbene disulphonic acid mixtures |
-
2010
- 2010-07-30 EP EP10171451.7A patent/EP2412870B1/en not_active Revoked
-
2011
- 2011-07-14 BR BR112013002342A patent/BR112013002342A2/en not_active Application Discontinuation
- 2011-07-14 CA CA2802544A patent/CA2802544A1/en not_active Abandoned
- 2011-07-14 US US13/813,160 patent/US20130126117A1/en not_active Abandoned
- 2011-07-14 WO PCT/EP2011/062081 patent/WO2012013513A1/en active Application Filing
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4670183A (en) * | 1983-11-15 | 1987-06-02 | The Dow Chemical Company | Method and compositions relating to the activation of fluorescent whitening agents |
US4717502A (en) * | 1985-01-23 | 1988-01-05 | Sandoz Ltd. | Aqueous optical brightener compositions |
US6025490A (en) * | 1997-02-18 | 2000-02-15 | Bayer Aktiengesellschaft | Process for the preparation of substituted 4,4'-diaminostilbene-2,2'-disulphonic acids |
US6365737B1 (en) * | 1998-02-20 | 2002-04-02 | Ciba Specialty Chemical Corporation | Process for the preparation of stilbene compounds |
US6165973A (en) * | 1999-02-05 | 2000-12-26 | Ciba Specialty Chemicals Corporation | Fluorescent whitening agent, its preparation and use |
US20030089888A1 (en) * | 2001-10-05 | 2003-05-15 | Erwin Bacher | Use of aqueous brightener preparations for brightening natural and synthetic materials |
US7258815B2 (en) * | 2002-04-19 | 2007-08-21 | Karl-Heinz Drenker | Use of brighteners for the preparation of coating slips |
US7731820B2 (en) * | 2004-10-27 | 2010-06-08 | Ciba Specialty Chemicals Corporation | Compositions of fluorescent whitening agents |
US7682438B2 (en) * | 2005-11-01 | 2010-03-23 | International Paper Company | Paper substrate having enhanced print density |
US20110126996A1 (en) * | 2008-06-11 | 2011-06-02 | Blankophor Gmbh & Co. Kg | Composition and process for whitening paper |
US20100129553A1 (en) * | 2008-11-27 | 2010-05-27 | International Paper Company | Optical Brightening Compositions For High Quality Inkjet Printing |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160177098A1 (en) * | 2013-03-21 | 2016-06-23 | Archroma Ip Gmbh | Optical brightening agents for high quality ink-jet printing |
US9868858B2 (en) * | 2013-03-21 | 2018-01-16 | Archroma Ip Gmbh | Optical brightening agents for high quality ink-jet printing |
US20160060814A1 (en) * | 2013-04-29 | 2016-03-03 | Blankophor Gmbh & Co., Kg | Use of Micronized Cellulose and Fluorescent Whitening Agent for Surface Treatment of Cellulosic Materials |
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EP2412870A1 (en) | 2012-02-01 |
CA2802544A1 (en) | 2012-02-02 |
EP2412870B1 (en) | 2013-04-17 |
WO2012013513A1 (en) | 2012-02-02 |
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