US20040149410A1 - Composition for the fluorescent whitening of paper - Google Patents

Composition for the fluorescent whitening of paper Download PDF

Info

Publication number
US20040149410A1
US20040149410A1 US10/478,728 US47872803A US2004149410A1 US 20040149410 A1 US20040149410 A1 US 20040149410A1 US 47872803 A US47872803 A US 47872803A US 2004149410 A1 US2004149410 A1 US 2004149410A1
Authority
US
United States
Prior art keywords
weight
composition
paper
fluorescent whitening
composition according
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.)
Abandoned
Application number
US10/478,728
Inventor
Peter Rohringer
Marc Grienenberger
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 Performance Products LLC
Original Assignee
Ciba Specialty Chemicals Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ciba Specialty Chemicals Corp filed Critical Ciba Specialty Chemicals Corp
Assigned to CIBA SPECIALTY CHEMICALS CORP. reassignment CIBA SPECIALTY CHEMICALS CORP. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GRIENENBERGER, MARC ROGER, ROHRINGER, PETER
Publication of US20040149410A1 publication Critical patent/US20040149410A1/en
Abandoned legal-status Critical Current

Links

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
    • 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
    • D21H21/06Paper forming aids
    • D21H21/10Retention agents or drainage improvers

Definitions

  • the present invention relates to a composition useful for the fluorescent whitening of paper in the pulp mass, in coatings or in the size press or metering size press.
  • FWA's fluorescent whitening agents
  • bentonite is not suitable for the stabilization of aqueous slurries and, furthermore, it has been found that, for example, hectorite exerts a far more efficient Increase In the retention of fillers than bentonite.
  • composition of the invention combines the advantages of these particular smectic, layered silicates with regard to their stabilizing influence of aqueous slurries with a vast improvement in filler retention, effects which are of high technical value for the paper-maker.
  • composition comprising
  • R 1 and R 2 independently represent C 1 -C 4 alkyl, C 2 -C 4 hydroxyalkyl or together complete a morpholine ring and
  • M is an alkaline or alkaline earth metal
  • the composition comprises 0.5 to 3%, more preferably 0.5 to 1.5%, by weight of hectorite, whilst, in a further preferred aspect, the composition comprises 0.5 to 5%, more preferably 0.5 to 1.5%, by weight of vermiculite.
  • R 1 and/or R 2 represent C 1 -C 4 alkyl, these may be methyl, ethyl, n- or isopropyl or n-, iso- or t-butyl, whilst C 2 -C 4 hydroxyalkyl may be hydroxyethyl, hydroxypropyl or hydroxybutyl.
  • M is an alkaline metal
  • this may be lithium, potassium or sodium, whilst an alkaline earth metal may be calcium or magnesium.
  • R 1 represents methyl, ethyl, hydroxyethyl or hydroxypropyl
  • R 2 represents hydroxyethyl or hydroxypropyl
  • M is lithium, potassium or sodium
  • a most preferable composition comprising a fluorescent whitening agent selected from the compounds of formulae
  • composition of the invention may comprise further adjuvants, for example, conserving agents such as 1,2-benzisothiazolin-2-one or aldehydes such as formaldehyde or acetaldehyde, anti-freeze agents or anti-foaming agents, whereby such adjuvants are normally employed in small quantities, for example, below 1% by weight.
  • conserving agents such as 1,2-benzisothiazolin-2-one or aldehydes such as formaldehyde or acetaldehyde
  • anti-freeze agents such as anti-foaming agents
  • composition of the invention may be obtained, for example, by intensive mixing of the FWA of formula (1), either in the form of a moist filter-cake or a dry powder, with water under high shear forces, subsequently, adding a pre-dispersion of hectorite and/or vermiculite in water and, finally stirring until a homogeneous mixture results, optionally, in the presence of appropriate adjuvants.
  • compositions are stable to storage over longer periods of time, for example, 6 months, even at temperatures ranging from 0° C. to 40° C.
  • composition of the present invention it has been found that it is possible to increase the whiteness of a lignin-containing pulp by 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 FWA.
  • the FWA composition 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 de-watering 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 composition of this invention is useful to produce significant whitening of chemical pulps as well as pulps containing up to 100% of mechanical fibre.
  • the composition can be employed, e.g. in lignin-free 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.
  • Addition of the composition of the invention to the pulp mass may be performed at any step of the paper-making process, but preferably is performed shortly before the head box.
  • chelating agents in processes to bleach pulps from mechanical pulping processes. See V. N. Gupta, Pulp Paper Mag. Can., 71 (18), T391-399 (1970).
  • the addition of 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 de-watering 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 FWA's and render them ineffective.
  • 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.
  • compositions 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 composition according to the present invention, to ensure that the treated paper contains 0.01 to 2 parts by weight, preferably 0.01 to 1 parts by weight, based on the white pigment, of the FWA (parts of the FWA 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. Pat. Nos. 3,265,654, 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 parts by weight, preferably 5 to 25 parts by weight, of the white pigment.
  • the amount of FWA composition used according to the invention is calculated so that the FWA is preferably present in amounts of 0.01 to 1 part by weight, more preferably 0.05 to 1 part by weight, and especially 0.05 to 0.6 parts 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 temperatures 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, water-soluble 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 water-soluble condensation products of formaldehyde with urea or melamine
  • polyphosphates or polyacrylic acid salts such as sodium binders, sodium bicarbonate, sodium
  • 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, in the size press or in the metering 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 FWA 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 60-10° C.) and excellent bleed-fastness to water.
  • the present invention provides a method for the fluorescent whitening 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 20 g/l of an FWA.
  • the size is starch, a starch derivative or a synthetic sizing agent, especially a water-soluble copolymer.
  • a formulation containing 16% of the compound (2) and 1% hectorite is obtained, which, as opposed to the starting formulation, is stable to storage.
  • Hand sheets are then prepared by means of the Rapid-Koethen System and the percentage retention of the filler is measured.

Abstract

A composition comprising a) 5 to 25% by weight of a fluorescent whitening agent of the formula (1), wherein R1 and R2 independently represent C1-C4alkyl, C2-C4hydroxyalkyl or together complete a morpholine ring and M is an alkaline or alkaline earth metal, b) 0.5 to 5% by weight of a swellable layered silicate which is hectorite and/or vermiculite, c) water and, optionally, d) further adjuvants and the use thereof for the fluorescent whitening of paper in the pulp mass, in coatings or in the size press or metering size press.
Figure US20040149410A1-20040805-C00001

Description

  • The present invention relates to a composition useful for the fluorescent whitening of paper in the pulp mass, in coatings or in the size press or metering size press. [0001]
  • Aqueous slurries of fluorescent whitening agents (FWA's) have been found to be advantageous in their applications in the paper industry, both from a technical and from an ecological point of view, as opposed to solutions, which necessitate considerable quantities of solvating agents such as urea or solvents such as polyalkylene glycols. [0002]
  • However, such aqueous slurries must be stable against sedimentation, serum formation and also to storage at elevated temperatures. Such stabilization has previously been achieved by the addition of polymers, such as xanthogenates and synthetic water-soluble polymers, or dispersing agents. [0003]
  • Surprisingly, it has now been found that particular smectic, layered silicates, namely hectorite and/or vermiculite, exhibit an excellent stabilizing influence on such aqueous slurries. [0004]
  • A further problem by the application of FWA's in the pulp mass is their property, not only not to enhance, but, indeed, in some cases, to reduce the retention of fillers. It has now been found that the quantities of hectorite and/or vermiculite useful for the stabilization of aqueous slurries also exert a very positive influence on the retention of fillers. Such effects are known in the case of bentonite. [0005]
  • However, bentonite is not suitable for the stabilization of aqueous slurries and, furthermore, it has been found that, for example, hectorite exerts a far more efficient Increase In the retention of fillers than bentonite. [0006]
  • Consequently, the composition of the invention combines the advantages of these particular smectic, layered silicates with regard to their stabilizing influence of aqueous slurries with a vast improvement in filler retention, effects which are of high technical value for the paper-maker. [0007]
  • The subject of the present invention is, thus, a composition comprising [0008]
  • a) 5 to 25%, preferably 10 to 20%, by weight of a fluorescent whitening agent of the formula [0009]
    Figure US20040149410A1-20040805-C00002
  • wherein R[0010]   1 and R2 independently represent C1-C4alkyl, C2-C4hydroxyalkyl or together complete a morpholine ring and
  • M is an alkaline or alkaline earth metal, [0011]
  • b) 0.5 to 5% by weight of a swellable layered silicate which is hectorite and/or vermiculite, [0012]
  • c) water and, optionally, [0013]
  • d) further adjuvants. [0014]
  • In one preferred aspect of the invention, the composition comprises 0.5 to 3%, more preferably 0.5 to 1.5%, by weight of hectorite, whilst, in a further preferred aspect, the composition comprises 0.5 to 5%, more preferably 0.5 to 1.5%, by weight of vermiculite. [0015]
  • When, in the compound of formula (1), R[0016] 1 and/or R2 represent C1-C4alkyl, these may be methyl, ethyl, n- or isopropyl or n-, iso- or t-butyl, whilst C2-C4hydroxyalkyl may be hydroxyethyl, hydroxypropyl or hydroxybutyl.
  • When, in the compound of formula (1), M is an alkaline metal, this may be lithium, potassium or sodium, whilst an alkaline earth metal may be calcium or magnesium. [0017]
  • Preferably, in the compound of formula (1), R[0018] 1 represents methyl, ethyl, hydroxyethyl or hydroxypropyl, R2 represents hydroxyethyl or hydroxypropyl, or R1 and R2 together complete a morpholine ring and M is lithium, potassium or sodium, a most preferable composition comprising a fluorescent whitening agent selected from the compounds of formulae
    Figure US20040149410A1-20040805-C00003
  • Optionally, the composition of the invention may comprise further adjuvants, for example, conserving agents such as 1,2-benzisothiazolin-2-one or aldehydes such as formaldehyde or acetaldehyde, anti-freeze agents or anti-foaming agents, whereby such adjuvants are normally employed in small quantities, for example, below 1% by weight. [0019]
  • The composition of the invention may be obtained, for example, by intensive mixing of the FWA of formula (1), either in the form of a moist filter-cake or a dry powder, with water under high shear forces, subsequently, adding a pre-dispersion of hectorite and/or vermiculite in water and, finally stirring until a homogeneous mixture results, optionally, in the presence of appropriate adjuvants. [0020]
  • The resulting compositions are stable to storage over longer periods of time, for example, 6 months, even at temperatures ranging from 0° C. to 40° C. [0021]
  • Using the composition of the present invention, it has been found that it is possible to increase the whiteness of a lignin-containing pulp by 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 FWA. While the FWA composition 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 de-watering and drying steps. Preferably it is added after completion of the last bleaching step. [0022]
  • By “a lignin-containing pulp” is meant any pulp that still contains about 5% or more of lignin by weight on a dry basis. By definition, 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. [0023]
  • The composition of this invention is useful to produce significant whitening of chemical pulps as well as pulps containing up to 100% of mechanical fibre. Thus the composition can be employed, e.g. in lignin-free 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. Preferably 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. [0024]
  • Addition of the composition of the invention to the pulp mass may be performed at any step of the paper-making process, but preferably is performed shortly before the head box. [0025]
  • It is known to employ chelating agents in processes to bleach pulps from mechanical pulping processes. See V. N. Gupta, Pulp Paper Mag. Can., 71 (18), T391-399 (1970). The addition of 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 de-watering steps. This decreases the incorporation of the heavy metal ions into the pulp. Additionally 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 FWA's and render them ineffective. [0026]
  • All types of 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). [0027]
  • Mixtures of thermodynamic and kinetic-controlling chelating agents (e.g. citrates, keto acids, gluconates, heptagluconates, phosphates, and phosphonates) also work well in reducing the content of free heavy metal ions in the pulp to acceptable levels. A number of these 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. [0028]
  • When used for the fluorescent whitening of paper, the compositions 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. [0029]
  • In a further aspect, 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 composition according to the present invention, to ensure that the treated paper contains 0.01 to 2 parts by weight, preferably 0.01 to 1 parts by weight, based on the white pigment, of the FWA (parts of the FWA per 100 parts of the pigment). [0030]
  • As 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. [0031]
  • 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. 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. Pat. Nos. 3,265,654, 3,657,174, 3,547,899 and 3,240,740. [0032]
  • 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. [0033]
  • Recipes for coating compositions for paper are described, for example, in J. P. Casey “Pulp and Paper”; Chemistry and Chemical Technology, 2nd edition, Volume III, pages1684-1649 and in “Pulp and Paper Manufacture”, 2nd and 5th edition, Volume II, page497 (McGraw-Hill). [0034]
  • 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 parts by weight, preferably 5 to 25 parts by weight, of the white pigment. The amount of FWA composition used according to the invention is calculated so that the FWA is preferably present in amounts of 0.01 to 1 part by weight, more preferably 0.05 to 1 part by weight, and especially 0.05 to 0.6 parts by weight, based on the white pigment. [0035]
  • The paper coating composition used in the method according to the invention can be prepared by mixing the components in any desired sequence at temperatures 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. Such 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, water-soluble condensation products of formaldehyde with urea or melamine, polyphosphates or polyacrylic acid salts. [0036]
  • 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. [0037]
  • 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, in the size press or in the metering 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. [0038]
  • By the use of the method according to the invention, the coatings obtained are distinguished by optimum distribution of the FWA 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 60-10° C.) and excellent bleed-fastness to water. [0039]
  • In a still further aspect, the present invention provides a method for the fluorescent whitening 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 20 g/l of an FWA. Preferably, the size is starch, a starch derivative or a synthetic sizing agent, especially a water-soluble copolymer. [0040]
  • The following examples further illustrate the invention, without intending to be restrictive in nature. Parts and percentages are by weight unless otherwise stated.[0041]
  • EXAMPLE 1
  • To 40 g of a 20% slurry formulation obtained from of 20% of the compound of formula (2) as solid crystals, 0.2% of a polysaccharide biopolymer and water, are added 10 g of a pre-dispersion prepared by the application of high shear forces to a mixture of 5 g of hectorite and 95 g of water for 15 minutes. The mixture is stirred until it is homogenous. [0042]
  • A formulation containing 16% of the compound (2) and 1% hectorite is obtained, which, as opposed to the starting formulation, is stable to storage. [0043]
  • Thus, after centrifuging at 3,500 rpm for 30 minutes, only 10% serum separation is observed as opposed to 50% for the starting 20% slurry. [0044]
  • Similarly, after storage at elevated temperature, 40% less serum formation is observed, in comparison to the starting 20% slurry. [0045]
  • EXAMPLE 2
  • To a fibre dispersion consisting of a mixture of birch and pine cellulose sulphates refined to 35[0046] 0SR, are added 20% and 40%, respectively, of precipitated calcium carbonate (PCC) as filler. Then, 0.01% or 0.05% of a cationic polyacrylamide (CPAM) as retention aid (Percol® 292) are added, followed by, after 3 minutes, sufficient of the slurry obtained according to Example 1 such that, together with the FWA of formula (2), 0.04% of hectorite, based on the weight of fibre, is present.
  • Hand sheets are then prepared by means of the Rapid-Koethen System and the percentage retention of the filler is measured. [0047]
  • The results are shown in the following Table 1, below, whereby, in the absence of both CPAM and hectorite, retention corresponds to 54% with 20% PCC and 53% with 40% PCC: [0048]
    TABLE 1
    20% PCC
    0.01% 40% PCC
    % Hectorite CPAM 0.05% CPAM 0.01% CPAM 0.05% CPAM
    None 70% 71% 56% 62%
    0.04 81% 88% 64% 70%
  • The results clearly demonstrate the improvement in the retention of PCC effected by the addition of extremely small quantities of hectorite. [0049]

Claims (13)

1. A composition comprising
a) 5 to 25% by weight of a fluorescent whitening agent of the formula
Figure US20040149410A1-20040805-C00004
 wherein
R1 and R2 independently represent C1-C4alkyl, C2-C4hydroxyalkyl or together complete a morpholine ring and
M is an alkaline or alkaline earth metal,
b) 0.5 to 5% by weight of a swellable layered silicate which is hectorite and/or vermiculite,
c) water and, optionally,
d) further adjuvants.
2. A composition according to claim 1 comprising 10 to 20% by weight of the fluorescent whitening agent of formula (1).
3. A composition according to claims 1 or 2 comprising 0.5 to 3% by weight of hectorite.
4. A composition according to claim 3 comprising 0.5 to 1.5% by weight of hectorite.
5. A composition according to claims 1 or 2 comprising 0.5 to 5% by weight of vermiculite.
6. A composition according to claim 5 comprising 0.5 to 1.5% by weight of vermiculite.
7. A composition according to any one of claims 1 to 6, wherein, In the fluorescent whitening agent of formula (1),
R1 represents methyl, ethyl, hydroxyethyl or hydroxypropyl,
R2 represents hydroxyethyl or hydroxypropyl or
R1 and R2 together complete a morpholine ring and
M represents lithium, potassium or sodium
8. A composition according to claim 7 wherein the fluorescent whitening agent is selected from the compounds of formulae
Figure US20040149410A1-20040805-C00005
9. Use of the composition according to any one of claims 1 to 8 for the fluorescent whitening of paper.
10. Use according to claim 9, whereby the composition is added to the pulp mass.
11. Use according to claim 9, whereby the composition is used for paper coating.
12. Use according to claim 9, whereby the composition is added to the size press or metering size press.
13. Paper, which has been optically brightened by the method according to claims 9 to 12.
US10/478,728 2001-05-29 2002-05-23 Composition for the fluorescent whitening of paper Abandoned US20040149410A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP01810521 2001-05-29
EP01810521.3 2001-05-29
PCT/EP2002/005668 WO2002097193A1 (en) 2001-05-29 2002-05-23 A composition for the fluorescent whitening of paper

Publications (1)

Publication Number Publication Date
US20040149410A1 true US20040149410A1 (en) 2004-08-05

Family

ID=8183935

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/478,728 Abandoned US20040149410A1 (en) 2001-05-29 2002-05-23 Composition for the fluorescent whitening of paper

Country Status (4)

Country Link
US (1) US20040149410A1 (en)
EP (1) EP1392925A1 (en)
AR (1) AR033770A1 (en)
WO (1) WO2002097193A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070131373A1 (en) * 2005-12-14 2007-06-14 Shevchenko Sergey M Method of decreasing the rate of photoyellowing
KR100735711B1 (en) 2006-01-09 2007-07-06 삼원산업주식회사 Fluorescent whitening agent and process of producing thereof
US20090250183A1 (en) * 2008-04-03 2009-10-08 Basf Se Paper coating or binding formulations and methods of making and using same
US20100210165A1 (en) * 2006-09-18 2010-08-19 Sca Hygiene Products Ab Multi-ply web of flexible material, such as paper and nonwoven, and product and method for improving the bleed fastness of a fluorescent whitening agent in adhesive zones of a multi-ply web

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10217677A1 (en) * 2002-04-19 2003-11-06 Bayer Ag Use of brighteners for the production of coating slips
DE102004038578A1 (en) * 2004-08-06 2006-03-16 Lanxess Deutschland Gmbh Alkanolammonium-containing Triazinylflavonataufheller
CN104862120A (en) * 2015-04-09 2015-08-26 广州立白企业集团有限公司 Preparation method of fluorescent brightener water solution for detergent

Citations (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4024071A (en) * 1975-01-22 1977-05-17 Ciba-Geigy Corporation 4,4'-Bis-(s-triazin-6-yl-amino)-stilbene-2,2'-disulphonic acid
US4339238A (en) * 1980-01-14 1982-07-13 Ciba-Geigy Corporation Stable aqueous formulations of stilbene fluorescent whitening agents
US4605511A (en) * 1978-07-17 1986-08-12 Ciba-Geigy Corporation Stable stilbene fluorescent brightener solution
US4888128A (en) * 1986-12-18 1989-12-19 Bayer Aktiengesellschaft Paper-coating slips containing fluorescent brighteners
US5071512A (en) * 1988-06-24 1991-12-10 Delta Chemicals, Inc. Paper making using hectorite and cationic starch
US5178730A (en) * 1990-06-12 1993-01-12 Delta Chemicals Paper making
US5234617A (en) * 1992-04-20 1993-08-10 Kathleen B. Hunter Aqueous liquid bleach compositions with fluorescent whitening agent and polyvinyl pyrrolidone or polyvinyl alcohol
US5296284A (en) * 1988-04-05 1994-03-22 J. M. Huber Corporation Dyed hectorite pigments and applications
US5429767A (en) * 1992-12-22 1995-07-04 Ciba-Geigy Corporation Storage-stable whitener formulation
US5473033A (en) * 1993-11-12 1995-12-05 W. R. Grace & Co.-Conn. Water-soluble cationic copolymers and their use as drainage retention aids in papermaking processes
US5518657A (en) * 1991-11-07 1996-05-21 Ciba-Geigy Corporation Storage-stable formulation of fluorescent whitening mixtures
US5622749A (en) * 1993-05-08 1997-04-22 Ciba-Geigy Corporation Fluorescent whitening of paper
US5976410A (en) * 1996-10-10 1999-11-02 Ciba Specialty Chemicals Corporation Dispersions of fluorescent whitening agents
US6063240A (en) * 1996-11-28 2000-05-16 Allied Colloids Limited Production of paper and paper board
US6096919A (en) * 1998-05-13 2000-08-01 Ciba Specialty Chemicals Corporation Process for the preparation of sulphonated distyryl-biphenyl compounds
US6228127B1 (en) * 1995-10-19 2001-05-08 Ciba Specialty Chemicals Corporation Bleaching or washing composition
US6302999B1 (en) * 1997-09-16 2001-10-16 Ciba Specialty Chemicals Corp. Method for optically brightening paper
US6537363B1 (en) * 1999-04-01 2003-03-25 Imerys Pigments, Inc. Kaolin pigments, their preparation and use
US6541440B2 (en) * 1995-10-12 2003-04-01 Süd-Chemie AG Washing-agent additive
US6564199B1 (en) * 1999-04-01 2003-05-13 Imerys Pigments, Inc. Kaolin clay pigments, their preparation and use
US6620294B1 (en) * 1999-08-13 2003-09-16 Ciba Specialty Chemicals Corporation Formulations of fluorescent whitening agents
US6764986B1 (en) * 1999-07-08 2004-07-20 Procter & Gamble Company Process for producing particles of amine reaction products
US6936078B2 (en) * 2000-06-19 2005-08-30 Ciba Specialty Chemicals Corp. Fluorescent brightener pigment compositions

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9610832D0 (en) * 1996-05-23 1996-07-31 Ciba Geigy Ag Stilbene compounds and their use
EP0905317B1 (en) * 1997-09-16 2009-12-23 Basf Se A method for optically brightening paper

Patent Citations (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4024071A (en) * 1975-01-22 1977-05-17 Ciba-Geigy Corporation 4,4'-Bis-(s-triazin-6-yl-amino)-stilbene-2,2'-disulphonic acid
US4605511A (en) * 1978-07-17 1986-08-12 Ciba-Geigy Corporation Stable stilbene fluorescent brightener solution
US4339238A (en) * 1980-01-14 1982-07-13 Ciba-Geigy Corporation Stable aqueous formulations of stilbene fluorescent whitening agents
US4888128A (en) * 1986-12-18 1989-12-19 Bayer Aktiengesellschaft Paper-coating slips containing fluorescent brighteners
US5296284A (en) * 1988-04-05 1994-03-22 J. M. Huber Corporation Dyed hectorite pigments and applications
US5071512A (en) * 1988-06-24 1991-12-10 Delta Chemicals, Inc. Paper making using hectorite and cationic starch
US5178730A (en) * 1990-06-12 1993-01-12 Delta Chemicals Paper making
US5518657A (en) * 1991-11-07 1996-05-21 Ciba-Geigy Corporation Storage-stable formulation of fluorescent whitening mixtures
US5234617A (en) * 1992-04-20 1993-08-10 Kathleen B. Hunter Aqueous liquid bleach compositions with fluorescent whitening agent and polyvinyl pyrrolidone or polyvinyl alcohol
US5429767A (en) * 1992-12-22 1995-07-04 Ciba-Geigy Corporation Storage-stable whitener formulation
US5622749A (en) * 1993-05-08 1997-04-22 Ciba-Geigy Corporation Fluorescent whitening of paper
US5473033A (en) * 1993-11-12 1995-12-05 W. R. Grace & Co.-Conn. Water-soluble cationic copolymers and their use as drainage retention aids in papermaking processes
US6541440B2 (en) * 1995-10-12 2003-04-01 Süd-Chemie AG Washing-agent additive
US6228127B1 (en) * 1995-10-19 2001-05-08 Ciba Specialty Chemicals Corporation Bleaching or washing composition
US5976410A (en) * 1996-10-10 1999-11-02 Ciba Specialty Chemicals Corporation Dispersions of fluorescent whitening agents
US6063240A (en) * 1996-11-28 2000-05-16 Allied Colloids Limited Production of paper and paper board
US6302999B1 (en) * 1997-09-16 2001-10-16 Ciba Specialty Chemicals Corp. Method for optically brightening paper
US20020084049A1 (en) * 1997-09-16 2002-07-04 Thomas Engelhardt Method for optically brightening paper
US6464832B2 (en) * 1997-09-16 2002-10-15 Ciba Specialty Chemicals Corporation Method for optically brightening paper
US6096919A (en) * 1998-05-13 2000-08-01 Ciba Specialty Chemicals Corporation Process for the preparation of sulphonated distyryl-biphenyl compounds
US6537363B1 (en) * 1999-04-01 2003-03-25 Imerys Pigments, Inc. Kaolin pigments, their preparation and use
US6564199B1 (en) * 1999-04-01 2003-05-13 Imerys Pigments, Inc. Kaolin clay pigments, their preparation and use
US6764986B1 (en) * 1999-07-08 2004-07-20 Procter & Gamble Company Process for producing particles of amine reaction products
US6620294B1 (en) * 1999-08-13 2003-09-16 Ciba Specialty Chemicals Corporation Formulations of fluorescent whitening agents
US6936078B2 (en) * 2000-06-19 2005-08-30 Ciba Specialty Chemicals Corp. Fluorescent brightener pigment compositions

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070131373A1 (en) * 2005-12-14 2007-06-14 Shevchenko Sergey M Method of decreasing the rate of photoyellowing
US8092649B2 (en) * 2005-12-14 2012-01-10 Nalco Company Method of decreasing the rate of photoyellowing with thiocyanic acid
KR100735711B1 (en) 2006-01-09 2007-07-06 삼원산업주식회사 Fluorescent whitening agent and process of producing thereof
US20100210165A1 (en) * 2006-09-18 2010-08-19 Sca Hygiene Products Ab Multi-ply web of flexible material, such as paper and nonwoven, and product and method for improving the bleed fastness of a fluorescent whitening agent in adhesive zones of a multi-ply web
US20090250183A1 (en) * 2008-04-03 2009-10-08 Basf Se Paper coating or binding formulations and methods of making and using same
US8613834B2 (en) * 2008-04-03 2013-12-24 Basf Se Paper coating or binding formulations and methods of making and using same
US9074322B2 (en) 2008-04-03 2015-07-07 Basf Se Paper coating or binding formulations and methods of making and using same

Also Published As

Publication number Publication date
WO2002097193A1 (en) 2002-12-05
AR033770A1 (en) 2004-01-07
EP1392925A1 (en) 2004-03-03

Similar Documents

Publication Publication Date Title
EP0712960B1 (en) Fluorescent whitening agent formulation
US6464832B2 (en) Method for optically brightening paper
US5622749A (en) Fluorescent whitening of paper
AU2005298779B2 (en) Compositions of fluorescent whitening agents
CN102597372B (en) Disulfo-type fluorescent whitening agents in coating applications
US7258815B2 (en) Use of brighteners for the preparation of coating slips
CA2217911C (en) Dispersions of fluorescent whitening agents
MXPA97007803A (en) Dispersions of fluorescen whitening agents
EP0905317B1 (en) A method for optically brightening paper
EP1674616B1 (en) Amphoteric fluorescent whitening agents
US20040149410A1 (en) Composition for the fluorescent whitening of paper
EP1294846A1 (en) Fluorescent brightener pigment compositions
GB2294708A (en) Fluorescent whitening agent formulation

Legal Events

Date Code Title Description
AS Assignment

Owner name: CIBA SPECIALTY CHEMICALS CORP., NEW YORK

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:ROHRINGER, PETER;GRIENENBERGER, MARC ROGER;REEL/FRAME:015308/0240

Effective date: 20030918

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION