Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
  • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
  • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
  • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
  • C07D251/40—Nitrogen atoms
  • C07D251/54—Three nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
• • 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
  • D21H19/00—Coated paper; Coating material
  • D21H19/36—Coatings with pigments

Definitions

• the instant invention relates to concentrated aqueous solutions of hexasulphonated stilbene optical brighteners which are storage-stable in the absence of solubilizing agents like urea.
• OWAs Hexasulphonated stilbene optical brightening agents
• Japanese Kokai 62-106965 discloses an optical brightener, or a salt thereof,
• R 1 and R 2 each independently represents a group selected from
• A represents a group selected from a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms, which may have a side chain, a hydroxymethyl group, a hydroxyethyl group, a methylthioethyl group, a benzyl group, a carboxymethyl group and a carboxyethyl group.
• said optical brighteners have a very high solubility in water and can be commercialized in the form of a thick solution after removing the sodium chloride produced in the reaction and concentrating the water content by an appropriate method.
• the optical brighteners are claimed to be very effective for the whitening of paper in a surface treatment.
• Each example of the Kokai describes the preparation of an optical brightener which is desalinated by ultrafiltration to give a thick solution. Supposing that in Example 1 the reaction of the starting compounds gives a 100% yield of said optical brightener then the maximal concentration in said thick solution would be 0.214 mol/kg (30-32%). Each solution is then rendered storage-stable by the addition of 10% urea.
• concentration of the aqueous solution is of particular significance when the brightener is applied in a pigmented coating composition; it is well-known that papermakers aim to minimise the water-content of the coating composition in order to minimise drying energy and to minimise water and binder migration into the base paper. (See, for example, 'The Essential Guide to Aqueous Coating of Paper and Board', ed. T. W. R. Dean, PITA, 1997.)
• hexasulphonated stilbene OBAs can be prepared in the form of highly concentrated aqueous solutions that are storage-stable at concentrations of up to 0.350 mol/kg (about 54% by weight).
• concentrations up to 0.350 mol/kg (about 54% by weight).
• An object of the present invention therefore is a storage-stable aqueous solution comprising an optical brightener of formula (1 )
• M is hydrogen, an alkali metal cation, ammonium, or ammonium which is mono-, di- or trisubstituted by a C 2 -C 3 -hydroxyalkyl radical, preferably hydrogen or a sodium cation, and n is from 1 to 4, preferably is 1 or 2,
• the amount of the optical brightener is higher than 0.214 mol/kg, preferably from 0.215 to 0.350 mol/kg, more particularly from 0.250 to 0.340 mol/kg, and that no solubilizing agent is contained in the solution.
• the aqueous solutions of the optical brightener(s) may optionally contain one or more carriers, antifreezes, preservatives, complexing agents etc., as well as organic byproducts formed during the preparation of the optical brightener.
• Carriers are known to give improved whitening characteristics and may be, e.g., polyethylene glycols, polyvinyl alcohols or carboxymethylcelluloses.
• Antifreezes may be, e.g., urea, diethylene glycol or triethylene glycol.
• the compounds of formula (1) are prepared by stepwise reaction of a cyanuric halide with a) a diamine of formula (A)
• cyanuric halide there may be employed the bromide or, preferably, the chloride.
• Each reaction may be carried out in an aqueous medium, the cyanuric halide being suspended in water, or in an aqueous/organic medium, the cyanuric halide being dissolved in a solvent such as acetone.
• Each amine may be introduced without dilution, or in the form of an aqueous solution or suspension.
• the amines can be reacted in any order, although it is preferred to react the aromatic amines first.
• Each amine may be reacted stoichiometrically, or in excess.
• the aromatic amines are reacted stoichimetrically, or in slight excess; the aliphatic amines are generally employed in an excess of 5-30% over stoichiometry.
• substitution of the first halogen of the cyanuric halide it is preferred to operate at a temperature in the range of 0 to 20°C, and under acidic to neutral pH conditions, preferably in the pH range of 2 to 7.
• substitution of the second halogen of the cyanuric halide it is preferred to operate at a temperature in the range of 20 to 60°C, and under weakly acidic to weakly alkaline conditions, preferably at a pH in the range of 4 to 8.
• substitution of the third halogen of the cyanuric halide it is preferred to operate at a temperature in the range of 60 to 102°C, and under weakly acidic to alkaline conditions, preferably at a pH in the range of 7 to 10.
• the pH may be controlled by addition of suitable acids or bases as necessary, preferred acids being e.g., hydrochloric acid, sulphuric acid, formic acid or acetic acid, preferred bases being e.g., alkali metal (e.g., lithium, sodium or potassium) hydroxides, carbonates or bicarbonates, or aliphatic tertiary amines e.g. triethanolamine or triisopropanolamine.
• suitable acids or bases as necessary, preferred acids being e.g., hydrochloric acid, sulphuric acid, formic acid or acetic acid, preferred bases being e.g., alkali metal (e.g., lithium, sodium or potassium) hydroxides, carbonates or bicarbonates, or aliphatic tertiary amines e.g. triethanolamine or triisopropanolamine.
• a further object of the instant invention is the process for the preparation of said aqueous solutions wherein the compounds of formula (1) are prepared as described above and wherein the alkali metal or amine salt that is generated as a by-product of each reaction between an amine and a cyanuric halide is removed from the reaction solution.
• a stable aqueous solution with a concentration of higher than 0.214 mol/kg (32-33% by weight), preferably from 0.214 to 0.350 mol/kg, more particularly from 0.250 to 0.340 mol/kg, of a compound of formula (1) without the addition of solubilizing aids such as ethylene glycol, urea or a mono-, di- or tri-(2-hydroxyethyl)- or (2-hydroxypropyl)-amine it is necessary to remove at least 50 %, preferably at least 80 % by weight, of the alkali metal or amine salt that is generated as a by-product of each reaction between an amine and a cyanuric halide. This is preferably done by ultrafiltration or membrane filtration of the solution formed as described above.
• the compound of formula (1 ) can be isolated by precipitation (e.g. by the addition of acid) then redissolved.
• a further object of the instant invention is the use of the instant storage-stable aqueous solutions for brightening of paper or other cellulosic substrates.
• the concentrated solutions of compounds of formula (1) are particularly suitable for the brightening of paper after sheet formation. This may be effected by adding the optical brightener solution to a pigmented coating composition, or to a sizing solution or suspension.
• the concentrated solutions of compounds of formula (1) are applied to the surface of paper in a pigmented coating composition.
• the coating compositions are essentially aqueous compositions that contain at least one binder and a white pigment, in particular an opacifying white pigment, and may additionally contain further additives such as dispersing agents and defoamers.
• white pigments are generally inorganic pigments, e.g., aluminium silicates (kaolin, otherwise known as china clay), calcium carbonate (chalk), titanium dioxide, aluminium hydroxide, barium carbonate, barium sulphate, or calcium sulphate (gypsum).
• aluminium silicates kaolin, otherwise known as china clay
• calcium carbonate chalk
• titanium dioxide aluminium hydroxide
• barium carbonate barium carbonate
• barium sulphate calcium sulphate
• the binders may be any of those commonly used in the paper industry for the production of coating compositions and may consist of a single binder or of a mixture of primary and secondary binders.
• the sole or primary binder is preferably a synthetic latex, typically a styrene-butadiene, vinyl acetate, styrene acrylic, vinyl acrylic or ethylene vinyl acetate polymer.
• the secondary binder may be, e.g., starch, carboxymethylcellulose, casein, soy polymers, or polyvinyl alcohol.
• the sole or primary binder is used in an amount typically in the range 5-25% by weight of white pigment.
• the secondary binder is used in an amount typically in the range 0.1- 2% by weight of white pigment; starch however is typically used in the range 5-10% by weight of white pigment.
• the optical brightener of formula (1) is used in an amount typically in the range 0.01- 1% by weight of white pigment, preferably in the range 0.05-0.5%) by weight of white pigment.
• a solution of 21.3 parts aniline-2,5-disulphonic acid and 6.7 parts sodium hydroxide in 30 parts water is added to a stirred suspension of 15.5 parts cyanuric chloride in 50 parts ice water.
• the pH is kept at 6 by the dropwise addition of 30% sodium hydroxide.
• the mixture is stirred below 10°C until primary aromatic amine groups can no longer be detected by the diazo reaction.
• a solution of 14.8 parts 4,4'-diaminostilbene-2,2'- disulphonic acid and 3.2 parts sodium hydroxide in 20 parts water is then added, the pH is adjusted to between 6.5 and 7.5 by the addition of 30% sodium hydroxide and the mixture is stirred at 30°C until a negative diazo reaction is obtained.
• a solution of 12.2 parts L-aspartic acid in 22.9 parts 16% sodium hydoxide is added, and the mixture is heated at reflux for 6 hours, the pH being kept at 7.5 to 8.5 by the addition of 30% sodium hydroxide.
• the aqueous solution so-formed of (2) in the form of its sodium salt, which is approximately 0.167 mol/kg in concentration, is desalinated by membrane filtration and concentrated to 0.330 mol/kg (50% by weight).
• the resulting solution, 2.0%) in sodium chloride has a viscosity of 0.23-0.25 Pa.s at 20°C and shows no signs of precipitation after 2 weeks at 5°C.
• An aqueous solution of (3) in the form of its sodium salt at a concentration of 0.330 mol/kg (51% by weight) is prepared as described in Example 1 but using 13.5 parts L- glutamic acid in place of 12.2 parts L-aspartic acid.
• the resulting solution, 2.0 % in sodium chloride, has a viscosity of 0.23-0.25 Pa.s at 20°C and shows no signs of precipitation after 2 weeks at 5°C.
• a coating composition is prepared containing 500 parts chalk (commercially available under the trade name Hydrocarb 90 from O YA), 500 parts clay (commercially available under the trade name Kaolin SPS from IMERYS), 470 parts water, 6 parts dispersing agent (a sodium salt of a polyacrylic acid commercially available under the trade name Polysalz S from BASF), 200 parts latex (an acrylic ester copolymer commercially available under the trade name Acronal S320D from BASF) and 30 parts of a 10% solution of carboxymethyl cellulose (commercially available under the trade name Finnfix 5.0 from Noviant) in water.
• the solids content is adjusted to 65% by the addition of water, and the pH is adjusted to 8-9 with sodium hydroxide.
• the brightened coating composition is then applied to a commercial 75 gsm neutral-sized white paper base sheet using an automatic wire- wound bar applicator with a standard speed setting and a standard load on the bar.
• the coated paper is then dried for 5 minutes in a hot air flow.
• the dried paper is allowed to condition, then measured for CIE Whiteness on a calibrated Elrepho spectrophotometer.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Paper (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Pigments, Carbon Blacks, Or Wood Stains (AREA)
• Coloring (AREA)

Priority Applications (7)

Applications Claiming Priority (2)

Publications (1)

Family

ID=34746007

Family Applications (1)

Country Status (14)

Families Citing this family (19)

Citations (3)

Family Cites Families (2)

• 2004
  • 2004-03-05 EP EP04005210A patent/EP1571149A1/en not_active Withdrawn
• 2005
  • 2005-02-05 TW TW094104029A patent/TW200602534A/zh unknown
  • 2005-02-17 RU RU2006131669/04A patent/RU2380364C2/ru active
  • 2005-02-17 BR BRPI0508459-8A patent/BRPI0508459A/pt not_active IP Right Cessation
  • 2005-02-17 WO PCT/IB2005/000407 patent/WO2005092868A1/en not_active Ceased
  • 2005-02-17 AU AU2005225623A patent/AU2005225623A1/en not_active Abandoned
  • 2005-02-17 CA CA002553556A patent/CA2553556A1/en not_active Abandoned
  • 2005-02-17 EP EP05702518A patent/EP1735290A1/en not_active Withdrawn
  • 2005-02-17 JP JP2007501362A patent/JP2007526383A/ja active Pending
  • 2005-02-17 CN CNA2005800066309A patent/CN1926120A/zh active Pending
  • 2005-02-17 US US10/591,572 patent/US20070186358A1/en not_active Abandoned
  • 2005-02-17 KR KR1020067017971A patent/KR20070008584A/ko not_active Ceased
  • 2005-03-02 PE PE2005000240A patent/PE20060182A1/es not_active Application Discontinuation
• 2006
  • 2006-08-11 ZA ZA200606681A patent/ZA200606681B/en unknown
  • 2006-09-01 NO NO20063924A patent/NO20063924L/no not_active Application Discontinuation

Patent Citations (3)

Non-Patent Citations (1)

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