EP0905317A1 - Procédé d'azurage optique de papier - Google Patents

Procédé d'azurage optique de papier Download PDF

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Publication number
EP0905317A1
EP0905317A1 EP98810889A EP98810889A EP0905317A1 EP 0905317 A1 EP0905317 A1 EP 0905317A1 EP 98810889 A EP98810889 A EP 98810889A EP 98810889 A EP98810889 A EP 98810889A EP 0905317 A1 EP0905317 A1 EP 0905317A1
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EP
European Patent Office
Prior art keywords
optical brightener
weight
alkyl
paper
formulation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP98810889A
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German (de)
English (en)
Other versions
EP0905317B1 (fr
Inventor
Thomas Engelhardt
Peter Rohringer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
Ciba Geigy AG
Ciba Spezialitaetenchemie Holding AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Publication date
Application filed by Ciba Geigy AG, Ciba Spezialitaetenchemie Holding AG filed Critical Ciba Geigy AG
Priority to EP19980810889 priority Critical patent/EP0905317B1/fr
Publication of EP0905317A1 publication Critical patent/EP0905317A1/fr
Application granted granted Critical
Publication of EP0905317B1 publication Critical patent/EP0905317B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/30Luminescent or fluorescent substances, e.g. for optical bleaching
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds
    • D21H17/67Water-insoluble compounds, e.g. fillers, pigments
    • D21H17/68Water-insoluble compounds, e.g. fillers, pigments siliceous, e.g. clays

Definitions

  • the present invention relates to a simplified method for increasing the whiteness of paper by the application of optical brighteners, also known as fluorescent whitening agents.
  • the subject of the present invention is hence a method for the optical brightening of paper, which comprises the use of a formulation essentially consisting of a swellable layered silicate and an optical brightener.
  • the swellable layered silicates are e.g. natural or synthetic clay minerals or sodium silicates.
  • a suitable natural clay mineral is e.g montmorillonite, beidelite, saponite, or hectorite; preferred synthetic species are the zeolites (type A, X or ⁇ , etc.) and acid- or alkaline-modified bentonites.
  • inventively used formulations may be in the form of a dry mixture or, alternatively, in the form of an aqueous dispersion.
  • the swellable layered silicates which are e.g. natural or synthetic clay minerals or synthetic sodium silicates, such as high opacity, high whiteness, ion-exchange properties and improved retention properties can simply be combined with the properties of the optical brighteners without loosing the desired fluorescence effect of the latter.
  • the aqueous formulation contains 0.1 to 15% by weight, preferably 1 to 10% by weight of optical brightener, based on the weight of the swellable layered silicate.
  • the formulation is in the form of an aqueous dispersion, this contains about 2 to 60% by weight of the swellable layered silicate.
  • the preferred range of the bentonites is about 2 to 25%., and mostly preferred 2 to 20%, by weight; for the synthetic zeolites the suitable range is about 2 to 50% by weight.
  • Dispersing agents such as polycondensates of naphthalene sulfonic acid and formaldehyde or lignin sulfonates can be used as auxiliaries.
  • the formulation is in the form of a dry mixture, this may contains 0,1 to 90% by weight preferably 1 to 50% by weight of the optical brightener, based on the weight of the swellable layered silicate.
  • the optical brightener used in the method of the present invention is preferably a derivative of 4,4'-bis-(triazinylamino)-stilbene-2,2'-disulphonic acid, a derivative of 4,4'-distyryl-biphenyl, or a derivative of dibenzofuranylbiphenyl.
  • the 4,4'-bis-(triazinylamino)-stilbene-2,2'- disulphonic acid optical brightener is of the formula: in which R 1 and R 2 , independently, are phenylamino, mono- or disulphonated phenylamino, morpholino, -N(CH 2 CH 2 OH) 2 , -N(CH 3 )(CH 2 CH 2 OH), -NH 2 , -N(C 1 -C 4 alkyl) 2 , -OCH 3, -Cl, NHCH 2 CH 2 SO 3 H, CH 2 CH 2 OH or ethanolaminopropionic acid amide; and M is H, Na, Li, K, Ca, Mg, ammonium, or ammonium that is mono-, di-, tri- or tetrasubstituted by C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl or a mixture thereof.
  • the 4,4'distyryl-biphenyl optical brightener is of the formula: in which R 3 and R 4 , independently, are H, SO 3 M, SO 2 N(C 1 -C 4 alkyl) 2 , O(C 1 -C 4 alkyl), CN, Cl, COO(C 1 -C 4 alkyl), CON(C 1 -C 4 alkyl) 2 or (CH 2 ) 3 N + (CH 3 ) 2 An - , in which M is H, Na, Li, K, Ca, Mg, ammonium, or ammonium that is mono-, di-, tri- or tetrasubstituted by C 1 -C 4 alkyl, C 1 -C 4 hydroxyalkyl or a mixture thereof and An is an anion, e.g. of a mineral acid (hydrochloric or sulfuric acid) or lower (C 1-4 )-carboxylic acid.
  • R 3 and R 4 independently, are H, SO 3 M, SO 2 N
  • Preferred compounds of formula (3) are those of the formula wherein M, R and R 1 have the indicated meanings, R and R 1 being preferably methyl.
  • optical brightener is of the formula: R x CH 2 CH 2 OH R x CH 3 or or mixtures of at least two of the compounds (5) to (10).
  • a process which comprises adding to an aqueous slurry comprising a lignin-containing pulp, during pulp manufacture, prior to the drying step or paper making step if the pulp is not isolated, an effective amount of an optical brightener.
  • the optical brightener can be added to the aqueous slurry comprising the lignin-containing pulp at any processing step, to minimize losses, it is advantageously added in the latter stages of pulp manufacture, prior to the final dewatering and drying steps. Preferably it is added after completion of the last bleaching step.
  • a lignin-containing pulp any pulp that still contains about 5% or more of lignin by weight on a dry basis.
  • lignin is that portion of the pulp which is insoluble in 72 weight percent sulfuric acid. Suitable test procedures for lignin content are given in TAPPI T 223 and ASTM D 1106.
  • the process of this invention is useful to produce significant whitening of pulps containing from about 5% lignin on a dry weight basis up to 100% of the lignin present in an equivalent amount of wood chips.
  • the process can be employed, e.g. on relatively low-lignin-containing pulps such as certain bleached kraft pulps up to and including higher lignin content pulps such as thermomechanical pulps, bleached chemi-thermomechanical pulps (CTMP), and even deinked bleached thermomechanical pulps.
  • the pulps contain at least 10% of lignin by weight on a dry weight basis; most preferably they contain at least 15%.
  • the range of brightness that can be obtained varies from about 50 to 90+ depending on starting pulp brightness and the type of pulp employed.
  • chelating agents in processes to bleach pulps from mechanical pulping processes. See V. N. Gupta , Pulp Paper Mag. Can., 71 (18), T391-399 (1970).
  • a chelating agent to an aqueous pulp slurry controls the natural yellowing tendency of glucuronic acids, extractives and lignin present in the pulp by removing or minimizing iron and other heavy metals such as copper, zinc and manganese metals that catalyze color-forming side reactions.
  • the iron and other heavy metals are converted into the form of their highly soluble chelates and largely removed in the dewatering steps. This decreases the incorporation of the heavy metal ions into the pulp.
  • the chelating agent sequesters the salts of iron and other heavy metals which remain and which, in their own right would otherwise relax the excited state of optical brighteners and render them ineffective .
  • this metal control step may be done as matter of course in pulping processes where reductive bleaching (e.g., bisulfite, hydrosulfite, or formamidine sulfite bleaching) or oxidative bleaching (e.g., peroxy- or peroxide bleaching) is employed.
  • reductive bleaching e.g., bisulfite, hydrosulfite, or formamidine sulfite bleaching
  • oxidative bleaching e.g., peroxy- or peroxide bleaching
  • the background level of residual iron and other heavy metals and their ions in wood chips is generally about 10-25 ppm, although it is rather dependent on geography and species considerations.
  • the amount of iron and other heavy metals and their ions in the water used in pulping mills varies widely. Significant additional amounts of iron and other heavy metals and their ions are introduced during mechanical pulping of wood chips as well as in recycling newsprint.
  • the amount of iron and other heavy metals and their ions in the aqueous pulp during manufacture is may be several hundred parts per million by weight, based on the dry weight of the pulp, at some stages of pulp manufacture.
  • a chelating agent is advantageously employed if the aqueous slurry comprising the lignin-containing pulp still contains from 25 to 500 ppm by weight, based on the dry weight of the pulp, of salts of iron and other heavy metals at the processing stage where the optical brightener is to be added.
  • Heavy metal contents can be determined by standard analytical procedures such as atomic absorption spectroscopy or inductively coupled plasma analysis. Once the type and amounts of the various heavy metals are known, the amount of the chelating agent to employ to reach 100 ppm or less, preferably about 25 ppm or less, can readily be calculated or determined from tables. It is not harmful to use a small excess.
  • the chelating agent selected and the degree of whiteness improvement desired from 0 up to about 1% by weight, based on the dry weight of the pulp, of a chelating agent may be advantageously employed
  • An additional and substantial benefit of chelate treatment is to open the fiber matrix to make it more accessible to the optical brightener.
  • chelating agents are suitable in the present invention, i.e. those that offer thermodynamic or kinetic control of metal ions. However preference is given to chelating agents that offer thermodynamic control, that is, chelating agents that form a stable, isolable, complex with a heavy metal ion. Within this group it is particularly preferred to use aminocarboxylic acid chelates.
  • Well known and commercially available members of this class include ethylenediaminetetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), hydroxyethylethylenediaminetriacetic acid (HEDTA) and nitrilotriacetic acid (NTA).
  • thermodynamic and kinetic-controlling chelating agents e.g. citrates, keto acids, gluconates, heptagluconates, phosphates, and phosphonates
  • thermodynamic and kinetic-controlling chelating agents also work well in reducing the content of free heavy metal ions in the pulp to acceptable levels.
  • kinetic-controlling chelating agents are also commercially available.
  • Kinetic controlling chelating agents are those which do not form a stable, isolable, complex with a heavy metal ion.
  • the formulations according to the present invention may also be applied to the paper substrate in the form of a paper coating composition or directly in the size press.
  • the present invention provides a method for the fluorescent whitening of a paper surface, comprising contacting the paper surface with a coating composition comprising a white pigment; a binder dispersion; optionally a water-soluble co-binder; and sufficient of a formulation according to the present invention, to ensure that the treated paper contains 0.01 to 2 % by weight, preferably 0.01 to 1% by weight, based on the white pigment, of the optical brightener (parts of the optical brightener per 100 parts of the pigment).
  • the white pigment component of the paper coating composition used according to the method of the present invention there are preferred inorganic pigments, e.g., aluminium or magnesium silicates, such as China clay and kaolin and, further, barium sulfate, satin white, titanium dioxide, calcium carbonate (chalk) or talcum; as well as white organic pigments.
  • inorganic pigments e.g., aluminium or magnesium silicates, such as China clay and kaolin and, further, barium sulfate, satin white, titanium dioxide, calcium carbonate (chalk) or talcum; as well as white organic pigments.
  • the paper coating compositions used according to the method of the present invention may contain, as binder, inter alia, plastics dispersions based on copolymers of butadiene/styrene, acrylonitrile/butadiene/styrene, acrylic acid esters, acrylic acid esters/styrene/acrylonitrile, ethylene/vinyl chloride and ethylene/vinyl acetate; or homopolymers, such as polyvinyl chloride, polyvinylidene chloride, polyethylene and polyvinyl acetate or polyurethanes.
  • plastics dispersions based on copolymers of butadiene/styrene, acrylonitrile/butadiene/styrene, acrylic acid esters, acrylic acid esters/styrene/acrylonitrile, ethylene/vinyl chloride and ethylene/vinyl acetate; or homopolymers, such as polyvinyl chloride, polyvinylidene chloride,
  • a preferred binder consists of styrene/butyl acrylate or styrene/butadiene/ acrylic acid copolymers or styrene/butadiene rubbers.
  • Other polymer latices are described, for example, in U.S.Patent Specifications3,265,654, 3,657,174, 3,547,899 and 3,240,740.
  • the optional water-soluble protective colloid may be, e.g., soya protein, casein, carboxymethylcellulose, natural or modified starch, chitosan or a derivative thereof or, especially, polyvinyl alcohol.
  • the preferred polyvinyl alcohol protective colloid component may have a wide range of saponification levels and molecular weights; e.g. a saponification level ranging from 40 to 100; and an average molecular weight ranging from 10,000 to 100,000.
  • the paper coating compositions used according to the method of the present invention preferably contain 10 to 70% by weight of a white pigment.
  • the binder is preferably used in an amount which is sufficient to make the dry content of polymeric compound up to 1 to 30% by weight, preferably 5 to 25% by weight, of the white pigment.
  • the amount of optical brightener preparation used according to the invention is calculated so that the optical brightener is preferably present in amounts of 0.01 to 1% by weight, more preferably 0.05 to 1% by weight, and especially 0.05 to 0.6% by weight, based on the white pigment.
  • the paper coating composition used in the method according to the invention can be prepared by mixing the components in any desired sequence at temperature from 10 to 100°C, preferably 20 to 80°C.
  • the components here also include the customary auxiliaries which can be added to regulate the rheological properties, such as viscosity or water retention capacity, of the coating compositions.
  • auxiliaries are, for example, natural binders, such as starch, casein, protein or gelatin, cellulose ethers, such as carboxyalkylcellulose or hydroxyalkylcellulose, alginic acid, alginates, polyethylene oxide or polyethylene oxide alkyl ethers, copolymers of ethylene oxide and propylene oxide, polyvinyl alcohol, watersoluble condensation products of formaldehyde with urea or melamine, polyphosphates or polyacrylic acid salts.
  • natural binders such as starch, casein, protein or gelatin
  • cellulose ethers such as carboxyalkylcellulose or hydroxyalkylcellulose
  • alginic acid alginates
  • polyethylene oxide or polyethylene oxide alkyl ethers copolymers of ethylene oxide and propylene oxide
  • polyvinyl alcohol watersoluble condensation products of formaldehyde with urea or melamine
  • polyphosphates or polyacrylic acid salts such as sodium binders, sodium bicarbonate, sodium s
  • the coating composition used according to the method of the present invention is preferably used to produce coated printed or writing paper, or special papers such as cardboard or photographic papers.
  • the coating composition used according to the method of the invention can be applied to the substrate by any conventional process, for example with an air blade, a coating blade, a roller, a doctor blade or a rod, or in the size press, after which the coatings are dried at paper surface temperatures in the range from 70 to 200°C, preferably 90 to 130°C, to a residual moisture content of 3-8%, for example with infra-red dryers and/or hot-air dryers. Comparably high degrees of whiteness are thus achieved even at low drying temperatures.
  • the coatings obtained are distinguished by optimum distribution of the dispersion optical brightener over the entire surface and by an increase in the level of whiteness thereby achieved, by a high fastness to light and to elevated temperature (e.g. stability for 24 hours at 60-100°C.) and excellent bleed-fastness to water.
  • the present invention provides a method for the optical brightening of a paper surface comprising contacting the paper in the size press or metering press with an aqueous preparation containing a size, optionally an inorganic or organic pigment and 0.1 to 20g/l of an optical brightener.
  • the size is starch, a starch derivative or a synthetic sizing agent, especially a water-soluble copolymer.
  • the layered silicates consist of natural or synthetic clay minerals or a layered sodium silicate, whereby the clay mineral is preferably montmorillonite, beidellite, saponite or hectorite.
  • the montmorillonite can be used in the sodium or calcium form or, respectively in the form of a calcium montmorillonite having been ion-exchanged with soda.
  • Synthetically prepared clay minerals of the above named groups may also be used.
  • synthetic layer-type sodium silicates for example the commercial product SKS 6 from Hoechst AG
  • SKS 6 from Hoechst AG
  • These layered silicates possess the property, by means of internal crystalline swelling, of being able to intercalate polar agents between the silicate lamella, resulting, at higher concentrations, in an increase in the distance between the layers.
  • the agglomerate particles of the formulation are preferably sheathed with a synthetic zeolite or layer-type sodium silicate (preferably ca 3 to 15% by weight) in order to increase their whiteness.
  • a synthetic zeolite or layer-type sodium silicate preferably ca 3 to 15% by weight
  • Further preferred alternatives for disguising the colouration of the formulation are either the addition of "bluing" dyes or pigments, for example Unidisperse RTM Blue B-E (commercial product of Ciba Specialty Chemicals Inc.), preferably in amounts of 0.3 to 5% by weight or the addition of coloured active substances such as the photobleaching agent Tinolux RTM BB (commercial product of Ciba Specialty Chemicals Inc.), preferably in amounts of 0.3 to 5% by weight.
  • the mixture is agitated for 15 minutes, then 0.03% of a cationic retention aid (Percol 292®) is added, and finally a handsheet is formed by using the Rapid Koethen system.
  • the dryed paper has an area weight of 160 g/m 2 .
  • the determination of the fluorescence is performed with a Datacolor Spectraflash 500.
  • the ISO-brightness is determined with and without a cut-off filter at 420 nm and the difference between these two measurements is the fluorescence.
  • Example 1 is repeated but using a slurry prepared from 5.0 g of the bentonite and 0.25 g of the compound of formula (8).
  • the ISO-brightness of the resulting paper increases from its initial value of 79.9 to 87.3, which results in a fluorescence value of 7.4.
  • the mixture is agitated for 15 minutes, then 0.03% of a cationic retention aid (Percol 292®) is added, and finally a handsheet is formed by using the Rapid Koethen system.
  • the dryed paper has an area weight of 160 g/m 2 .

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EP19980810889 1997-09-16 1998-09-08 Procédé d'azurage optique de papier Expired - Lifetime EP0905317B1 (fr)

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EP97810668 1997-09-16
EP97810668 1997-09-16
EP19980810889 EP0905317B1 (fr) 1997-09-16 1998-09-08 Procédé d'azurage optique de papier

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Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002097193A1 (fr) * 2001-05-29 2002-12-05 Ciba Specialty Chemicals Holding Inc. Composition de blanchiment fluorescent du papier
KR100375888B1 (ko) * 2000-08-01 2003-03-15 이석기 수팽윤성 점토를 함유한 수성코팅제의 제조방법
WO2003044275A1 (fr) * 2001-11-21 2003-05-30 Clariant International Ltd Ameliorations portant sur des azurants optiques
WO2003104560A1 (fr) * 2002-06-11 2003-12-18 Ciba Specialty Chemicals Holding Inc. Pigments de blanchiment
WO2005014932A1 (fr) * 2003-08-06 2005-02-17 Ciba Specialty Chemicals Holding Inc. Composition de blanchiment fluorescent de papier
WO2007104128A1 (fr) * 2006-03-13 2007-09-20 Fp Innovations DECOLORATION de pulpe par dioxyde de chlore presque neutre
WO2007143184A2 (fr) * 2006-06-02 2007-12-13 International Paper Company Pulpe et papier de brillance améliorée
WO2007143182A2 (fr) * 2006-06-02 2007-12-13 International Paper Company Procédé amélioré de fabrication de pulpe, de papier et de produits en carton
WO2008017623A1 (fr) * 2006-08-08 2008-02-14 Clariant International Ltd Solutions aqueuses d'azurants optiques
WO2008036038A1 (fr) * 2006-09-18 2008-03-27 Sca Hygiene Products Ab Bande multi-pli de matière souple, tel que du papier et du non-tissé, et produit et procédé pour améliorer la rapidité de dégorgement d'un agent blanchissant fluorescent dans des zones adhésives d'une bande multi-pli
WO2009110824A1 (fr) * 2008-03-07 2009-09-11 Sca Hygiene Products Ab Bande à multiples plis de matériau souple, tel qu'un papier mince ou un non-tissé, et produit, et procédé pour améliorer la rapidité de dégorgement d'un agent blanchissant fluorescent d'une bande à multiples plis
US7758934B2 (en) 2007-07-13 2010-07-20 Georgia-Pacific Consumer Products Lp Dual mode ink jet paper
AU2006235427B2 (en) * 2005-04-08 2011-02-03 Nalco Company Improved composition and processes for paper production
ITMI20100662A1 (it) * 2010-04-19 2011-10-20 3V Sigma Spa Miscela, composizione e processo per il trattamento superficiale della carta
US8246780B2 (en) * 2005-09-19 2012-08-21 Nalco Company Methods for enhancing brightness and resistance to thermal yellowing of bleached kraft pulp and paper
US9932709B2 (en) 2013-03-15 2018-04-03 Ecolab Usa Inc. Processes and compositions for brightness improvement in paper production

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CH548484A (de) 1970-08-19 1974-04-30 Sandoz Ag Aufhellpraeparat.
FR2355955A1 (fr) 1976-06-25 1978-01-20 Mobil Oil Procede pour ameliorer l'effet des azurants optiques dans l'industrie du papier
EP0274666A1 (fr) * 1986-12-18 1988-07-20 Bayer Ag Compositions de couchage pour papier comprenant des agents de blanchiment
EP0588768A2 (fr) * 1992-09-14 1994-03-23 Ciba-Geigy Ag Procédé d'amélioration du degré de blancheur, de l'éclat et du lieu de couleur de matières de charge et de pigments
DE19538029A1 (de) * 1995-10-12 1997-04-17 Sued Chemie Ag Waschmittelzusatz
US5622749A (en) 1993-05-08 1997-04-22 Ciba-Geigy Corporation Fluorescent whitening of paper

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH409981A (de) 1959-11-20 1966-03-31 Geigy Ag J R Stabiles, konzentriertes, flüssiges Aufhellerpräparat sowie Verfahren zu seiner Herstellung und Verwendung des Präparates
CH548484A (de) 1970-08-19 1974-04-30 Sandoz Ag Aufhellpraeparat.
FR2355955A1 (fr) 1976-06-25 1978-01-20 Mobil Oil Procede pour ameliorer l'effet des azurants optiques dans l'industrie du papier
EP0274666A1 (fr) * 1986-12-18 1988-07-20 Bayer Ag Compositions de couchage pour papier comprenant des agents de blanchiment
EP0588768A2 (fr) * 1992-09-14 1994-03-23 Ciba-Geigy Ag Procédé d'amélioration du degré de blancheur, de l'éclat et du lieu de couleur de matières de charge et de pigments
US5622749A (en) 1993-05-08 1997-04-22 Ciba-Geigy Corporation Fluorescent whitening of paper
DE19538029A1 (de) * 1995-10-12 1997-04-17 Sued Chemie Ag Waschmittelzusatz

Cited By (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100375888B1 (ko) * 2000-08-01 2003-03-15 이석기 수팽윤성 점토를 함유한 수성코팅제의 제조방법
WO2002097193A1 (fr) * 2001-05-29 2002-12-05 Ciba Specialty Chemicals Holding Inc. Composition de blanchiment fluorescent du papier
WO2003044275A1 (fr) * 2001-11-21 2003-05-30 Clariant International Ltd Ameliorations portant sur des azurants optiques
US7198731B2 (en) 2001-11-21 2007-04-03 Clariant Finance (Bvi) Limited Optical brighteners
AU2002347452B2 (en) * 2001-11-21 2008-01-31 Clariant Finance (Bvi) Limited Improvements relating to optical brighteners
KR100952554B1 (ko) * 2001-11-21 2010-04-12 클라리언트 파이넌스 (비브이아이)리미티드 광학 표백제와 관련된 개선
WO2003104560A1 (fr) * 2002-06-11 2003-12-18 Ciba Specialty Chemicals Holding Inc. Pigments de blanchiment
WO2005014932A1 (fr) * 2003-08-06 2005-02-17 Ciba Specialty Chemicals Holding Inc. Composition de blanchiment fluorescent de papier
US7638016B2 (en) 2005-02-19 2009-12-29 International Paper Company Method for treating kraft pulp with optical brighteners after chlorine bleaching to increase brightness
AU2006235427B2 (en) * 2005-04-08 2011-02-03 Nalco Company Improved composition and processes for paper production
US8246780B2 (en) * 2005-09-19 2012-08-21 Nalco Company Methods for enhancing brightness and resistance to thermal yellowing of bleached kraft pulp and paper
WO2007104128A1 (fr) * 2006-03-13 2007-09-20 Fp Innovations DECOLORATION de pulpe par dioxyde de chlore presque neutre
WO2007143182A2 (fr) * 2006-06-02 2007-12-13 International Paper Company Procédé amélioré de fabrication de pulpe, de papier et de produits en carton
WO2007143184A3 (fr) * 2006-06-02 2008-03-06 Int Paper Co Pulpe et papier de brillance améliorée
WO2007143182A3 (fr) * 2006-06-02 2008-03-06 Int Paper Co Procédé amélioré de fabrication de pulpe, de papier et de produits en carton
US7967948B2 (en) 2006-06-02 2011-06-28 International Paper Company Process for non-chlorine oxidative bleaching of mechanical pulp in the presence of optical brightening agents
WO2007143184A2 (fr) * 2006-06-02 2007-12-13 International Paper Company Pulpe et papier de brillance améliorée
WO2008017623A1 (fr) * 2006-08-08 2008-02-14 Clariant International Ltd Solutions aqueuses d'azurants optiques
CN101553531B (zh) * 2006-08-08 2012-06-27 克莱里安特财务(Bvi)有限公司 荧光增白剂水溶液
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ITMI20100662A1 (it) * 2010-04-19 2011-10-20 3V Sigma Spa Miscela, composizione e processo per il trattamento superficiale della carta
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