WO2008017585A1 - Aqueous solutions of optical brighteners - Google Patents
Aqueous solutions of optical brighteners Download PDFInfo
- Publication number
- WO2008017585A1 WO2008017585A1 PCT/EP2007/057591 EP2007057591W WO2008017585A1 WO 2008017585 A1 WO2008017585 A1 WO 2008017585A1 EP 2007057591 W EP2007057591 W EP 2007057591W WO 2008017585 A1 WO2008017585 A1 WO 2008017585A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- optical brightener
- polyvinyl alcohol
- white pigment
- solutions
- Prior art date
Links
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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/41—Compounds containing sulfur bound to oxygen
- C08K5/42—Sulfonic acids; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L29/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
- C08L29/02—Homopolymers or copolymers of unsaturated alcohols
- C08L29/04—Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
-
- 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
- D21H19/44—Coatings with pigments characterised by the other ingredients, e.g. the binder or dispersing agent
- D21H19/46—Non-macromolecular organic compounds
Definitions
- the instant invention relates to aqueous solutions of optical brighteners with polyvinyl alcohols which can be directly used by the papermaker and which provide coated papers of high whiteness.
- PVOH polyvinyl alcohol
- WO 2005/056658 seeks to provide a solution by disclosing a method of preparing an optical brightener/PVOH aqueous concentrate comprising the sequential steps of: (a) providing an aqueous brightener composition including water and optical brightener active ingredient, wherein the optical brightener active ingredient is typically present in the aqueous brightener composition in an amount of from about 10% to about 25%; (b) admixing a polyvinyl alcohol resin with said optical brightener composition in an amount of about 1 part of dry polyvinyl alcohol resin per 0.25 to 10 wet parts of aqueous brightener composition to provide a nascent aqueous concentrate of polyvinyl alcohol resin and optical brightener; and (c) cooking the aqueous concentrate to dissolve the solids (i.e., to give an aqueous solution containing optical brightener and 9.1-80% polyvinyl alcohol).
- WO 2005/056658 does not however provide a satisfactory solution for the papermaker, who would typically wish to meter the optical brightener/PVOH solution directly into the coating composition; aqueous solutions containing optical brightener and more than 9% PVOH are generally of such high viscosity that they can be pumped only with difficulty, if at all. Papermakers are typically not able to use liquids with a viscosity greater than 1,000 mPa.s not only because of pumping difficulties, but also because of shock thickening when a liquid of such high viscosity is introduced to the coating composition.
- WO 98/42685 discloses in example 15 an aqueous coating composition containing 40 weight % water, 40 parts clay, 60 parts calcium carbonate and 0.2 part polyvinyl alcohol to which 0.2% or 0.4% of a fluorescent whitening agent is added. There is no suggestion in this document that much higher concentrations of polyvinyl alcohol and of optical brightener would still lead to pumpable compositions for the papermaker.
- US 2003/0089888 Al discloses aqueous brightener preparations containing as organic thickener polyvinyl alcohol with a degree of hydrolysis of more than 70% and where the temperature of said preparation is from 40 to 98°C.
- optical brightener/PVOH solutions of low viscosity which may be used directly by the papermaker, in that they can be metered by pump directly into a coating composition, and which provide coated papers of a surprisingly high whiteness.
- the invention thus provides aqueous optical brightener solutions consisting of
- M is hydrogen, an alkali metal atom, ammonium or a cation derived from an amine, preferably hydrogen or sodium, most preferably sodium, n is 1 or 2, and
- X is a natural or unnatural amino acid from which a hydrogen atom of the amino group has been removed;
- the SO3M group is preferably in the 4-position of the phenyl ring.
- the SO3M groups are preferably in the 2,5- positions of the phenyl ring.
- amino acids from which X may be derived are alanine, 2-amino butyric acid, asparagine, aspartic acid, S-carboxymethylcysteine, cysteic acid, cysteine, glutamic acid, glutamine, glycine, iminodiacetic acid, iso leucine, leucine, methionine, N-methyltaurine, norleucine, norvaline, phenylalanine, 2-phenylglycine, pipecolinic acid, proline, sarcosine, serine, taurine, threonine, and valine. Where the amino acid contains a chiral centre, either optical isomer, or the racemic mixture, can be used.
- Preferred amino acids are aspartic acid, glutamic acid and iminodiacetic acid.
- the aqueous solutions may contain up to 10% by weight of salt, typically sodium chloride, formed as a by-product from the production of the optical brightener.
- salt typically sodium chloride
- the aqueous solutions may also contain one or more antifreezes, biocides, complexing agents or other additives, as well as organic by-products formed during the preparation of the optical brightener.
- the aqueous solution may also contain other carriers, such as polyethylene glycol.
- the polyvinyl alcohol preferably has a degree of hydrolysis in the range 65-75% and a Brookf ⁇ eld viscosity of 2-20 mPa.s (4% aqueous solution at 2O 0 C).
- the polyvinyl alcohol content of the solution lies in the range 1 to 5% by weight.
- the concentration of the optical brightener in the solution is preferably in the range 10 to 50% by weight.
- optical brightener/PVOH solutions are typically made by adding the polyvinyl alcohol as a solid to a stirred solution of the optical brightener in water, and heating to 90-95 0 C until a clear solution forms.
- the pH of the aqueous solution is preferably from neutral to clearly alkaline, in particular in the range pH 7 to pH 10.
- the pH may, if necessary, be adjusted by addition of M-corresponding bases, e.g. alkali metal hydroxides or carbonates, ammonia or amines.
- optical brightener/PVOH solutions of the invention are storage-stable and may be used directly as such, in that they may be metered by pump directly into a coating composition.
- a further object of the invention is the addition of the brightener/PVOH solutions to coating compositions in order to obtain a coated and optically brightened paper.
- the invention also provides a process for the production of coated paper that is optically brightened at least in the coating, wherein a coating composition as described above is coated onto paper after sheet formation.
- 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, defoamers and synthetic thickeners.
- 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, polyvinyl alcohol or a mixture of any of the above.
- 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- 10% by weight of white pigment.
- 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.
- Optical brightener solution 1 is produced by stirring together
- Brookf ⁇ eld viscosity of 6.0 mPa.s (4% aqueous solution at 2O 0 C) while heating to 90-95 0 C, until a clear solution is obtained that remains stable after cooling to room temperature.
- the pH of the solution is adjusted to 9.0 with sodium hydroxide.
- the viscosity of the solution is 10.4 mPa.s at 2O 0 C and 14.3 mPa.s at 1O 0 C.
- Optical brightener solution 2 is produced by stirring together 18.5 parts of an optical brightener of formula (2), 79.1 parts of water, and
- the viscosity of the solution is 31.3 mPa.s at 2O 0 C and 48.1 mPa.s at 1O 0 C.
- Optical brightener solution 3 is produced by stirring together 18.5 parts of an optical brightener of formula (2), and
- a coating composition is prepared containing 500 parts chalk (commercially available under the trade name Hydrocarb 90 from OMYA), 500 parts clay (commercially available under the trade name Kaolin SPS from IMERYS), 370 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 of 50% latex (a styrene butadiene copolymer commercially available under the trade name DL 921 from Dow) and 400 parts of a 20% solution of an anionic potato starch (Perfectamyl A4692 from AVEBE B. A.) in water.
- the solids content is adjusted to 60% by the addition of water, and the pH is adjusted to 8-9 with sodium hydroxide.
- Optical brightener solutions 1, 2 and 3, made as described in Preparative Examples 1, 2 and 3 respectively, are added at a range of concentrations from 0.4 to 1.0% by weight of dry solids to the stirred coating composition.
- the brightened coating composition is then applied to a commercial 75 g/m 2 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.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paper (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BRPI0715395-3A BRPI0715395A2 (en) | 2003-08-08 | 2007-07-24 | aqueous solutions of apical bleaches |
JP2009523236A JP2010500429A (en) | 2006-08-08 | 2007-07-24 | Aqueous whitening solution |
CA002659540A CA2659540A1 (en) | 2006-08-08 | 2007-07-24 | Aqueous solutions of optical brighteners |
US12/376,691 US20100175845A1 (en) | 2006-08-08 | 2007-07-24 | Aqueous Solutions Of Optical Brighteners |
EP07787834A EP2052021A1 (en) | 2006-08-08 | 2007-07-24 | Aqueous solutions of optical brighteners |
AU2007283705A AU2007283705A1 (en) | 2006-08-08 | 2007-07-24 | Aqueous solutions of optical brighteners |
IL196910A IL196910A0 (en) | 2006-08-08 | 2009-02-05 | Aqueous solutions of optical brighteners |
NO20090599A NO20090599L (en) | 2006-08-08 | 2009-02-06 | Aqueous solutions of optical brighteners |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06118571.6 | 2006-08-08 | ||
EP06118571 | 2006-08-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008017585A1 true WO2008017585A1 (en) | 2008-02-14 |
Family
ID=37709464
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2007/057591 WO2008017585A1 (en) | 2003-08-08 | 2007-07-24 | Aqueous solutions of optical brighteners |
Country Status (15)
Country | Link |
---|---|
US (1) | US20100175845A1 (en) |
EP (1) | EP2052021A1 (en) |
JP (1) | JP2010500429A (en) |
KR (1) | KR20090058516A (en) |
CN (1) | CN101547968A (en) |
AR (1) | AR062275A1 (en) |
AU (1) | AU2007283705A1 (en) |
BR (1) | BRPI0715395A2 (en) |
CA (1) | CA2659540A1 (en) |
IL (1) | IL196910A0 (en) |
NO (1) | NO20090599L (en) |
RU (1) | RU2009107918A (en) |
TW (1) | TW200815644A (en) |
WO (1) | WO2008017585A1 (en) |
ZA (1) | ZA200900904B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009154898A1 (en) * | 2008-06-20 | 2009-12-23 | International Paper Company | Composition and recording sheet with improved optical properties |
EP2356183B1 (en) | 2008-12-08 | 2015-06-03 | Hewlett-Packard Development Company, L.P. | Surface coating composition for inkjet media |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1712677A1 (en) * | 2005-04-08 | 2006-10-18 | Clariant International Ltd. | Aqueous solutions of optical brighteners |
EP2426657B1 (en) * | 2009-04-28 | 2016-08-03 | Yuugengaisha Seiwadental | Organ model |
JP4841663B2 (en) | 2009-09-30 | 2011-12-21 | 仁夫 岡野 | Vascular model for practicing stent graft insertion or aneurysm and suture surgery for aneurysms |
JP5886843B2 (en) * | 2010-07-01 | 2016-03-16 | クラリアント・ファイナンス・(ビーブイアイ)・リミテッド | Aqueous composition for color adjustment in coating applications |
WO2012000624A1 (en) * | 2010-07-01 | 2012-01-05 | Clariant International Ltd | Aqueous compositions for whitening and shading in coating applications |
EP3077454A1 (en) | 2013-12-06 | 2016-10-12 | Monosol, LLC | Fluorescent tracer for water-soluble films, related methods, and related articles |
JP6389447B2 (en) * | 2015-08-07 | 2018-09-12 | 北越コーポレーション株式会社 | Coated paper for printing |
CN105907129A (en) * | 2016-04-26 | 2016-08-31 | 浙江珊瑚化工有限公司 | Emulsion containing fluorescent whitening agent |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998042685A1 (en) * | 1997-03-25 | 1998-10-01 | Ciba Specialty Chemicals Holding Inc. | Fluorescent whitening agents |
US20030089888A1 (en) * | 2001-10-05 | 2003-05-15 | Erwin Bacher | Use of aqueous brightener preparations for brightening natural and synthetic materials |
WO2005056658A1 (en) * | 2003-12-09 | 2005-06-23 | Celanese International Corporation | Optical brightener and method of preparing it |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3479349A (en) * | 1967-08-03 | 1969-11-18 | Geigy Chem Corp | Polysulfonated bis-s-triazinylamino-stilbene-2,2'-disulfonic acids |
KR100607533B1 (en) * | 1998-08-25 | 2006-08-02 | 클라리언트 파이넌스 (비브이아이)리미티드 | Aqueous compositions of uv-active agents, their production and use |
DE19960862A1 (en) * | 1999-12-17 | 2001-06-28 | Basf Ag | Paper coating slips with increased water retention |
JP4179584B2 (en) * | 2001-03-22 | 2008-11-12 | 日本化薬株式会社 | Aqueous liquid composition of fluorescent brightener with excellent dyeing properties |
-
2007
- 2007-07-24 BR BRPI0715395-3A patent/BRPI0715395A2/en not_active Application Discontinuation
- 2007-07-24 CN CNA200780029366XA patent/CN101547968A/en active Pending
- 2007-07-24 WO PCT/EP2007/057591 patent/WO2008017585A1/en active Application Filing
- 2007-07-24 KR KR1020097004658A patent/KR20090058516A/en not_active Application Discontinuation
- 2007-07-24 JP JP2009523236A patent/JP2010500429A/en not_active Withdrawn
- 2007-07-24 EP EP07787834A patent/EP2052021A1/en not_active Withdrawn
- 2007-07-24 CA CA002659540A patent/CA2659540A1/en not_active Abandoned
- 2007-07-24 RU RU2009107918/05A patent/RU2009107918A/en not_active Application Discontinuation
- 2007-07-24 US US12/376,691 patent/US20100175845A1/en not_active Abandoned
- 2007-07-24 AU AU2007283705A patent/AU2007283705A1/en not_active Abandoned
- 2007-08-06 TW TW096128886A patent/TW200815644A/en unknown
- 2007-08-07 AR ARP070103488A patent/AR062275A1/en unknown
-
2009
- 2009-02-05 IL IL196910A patent/IL196910A0/en unknown
- 2009-02-06 NO NO20090599A patent/NO20090599L/en not_active Application Discontinuation
- 2009-02-06 ZA ZA200900904A patent/ZA200900904B/en unknown
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998042685A1 (en) * | 1997-03-25 | 1998-10-01 | Ciba Specialty Chemicals Holding Inc. | Fluorescent whitening agents |
US20030089888A1 (en) * | 2001-10-05 | 2003-05-15 | Erwin Bacher | Use of aqueous brightener preparations for brightening natural and synthetic materials |
WO2005056658A1 (en) * | 2003-12-09 | 2005-06-23 | Celanese International Corporation | Optical brightener and method of preparing it |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009154898A1 (en) * | 2008-06-20 | 2009-12-23 | International Paper Company | Composition and recording sheet with improved optical properties |
US8361571B2 (en) | 2008-06-20 | 2013-01-29 | International Paper Company | Composition and recording sheet with improved optical properties |
RU2507335C2 (en) * | 2008-06-20 | 2014-02-20 | Интернэшнл Пэйпа Кампани | Composition and sheet for records with improved optical characteristics |
EP2787120A1 (en) * | 2008-06-20 | 2014-10-08 | International Paper Company | Recording sheet with improved optical properties |
US8906476B2 (en) | 2008-06-20 | 2014-12-09 | International Paper Company | Composition and recording sheet with improved optical properties |
US9745700B2 (en) | 2008-06-20 | 2017-08-29 | International Paper Company | Composition and recording sheet with improved optical properties |
EP2356183B1 (en) | 2008-12-08 | 2015-06-03 | Hewlett-Packard Development Company, L.P. | Surface coating composition for inkjet media |
EP2356183B2 (en) † | 2008-12-08 | 2021-01-27 | Hewlett-Packard Development Company, L.P. | Surface coating composition for inkjet media |
Also Published As
Publication number | Publication date |
---|---|
NO20090599L (en) | 2009-05-08 |
IL196910A0 (en) | 2009-11-18 |
BRPI0715395A2 (en) | 2013-06-25 |
RU2009107918A (en) | 2010-09-20 |
AR062275A1 (en) | 2008-10-29 |
CA2659540A1 (en) | 2008-02-14 |
CN101547968A (en) | 2009-09-30 |
KR20090058516A (en) | 2009-06-09 |
TW200815644A (en) | 2008-04-01 |
JP2010500429A (en) | 2010-01-07 |
US20100175845A1 (en) | 2010-07-15 |
EP2052021A1 (en) | 2009-04-29 |
AU2007283705A1 (en) | 2008-02-14 |
ZA200900904B (en) | 2010-04-28 |
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