WO2007050964A1 - Grease and water resistant article - Google Patents

Grease and water resistant article Download PDF

Info

Publication number
WO2007050964A1
WO2007050964A1 PCT/US2006/042149 US2006042149W WO2007050964A1 WO 2007050964 A1 WO2007050964 A1 WO 2007050964A1 US 2006042149 W US2006042149 W US 2006042149W WO 2007050964 A1 WO2007050964 A1 WO 2007050964A1
Authority
WO
WIPO (PCT)
Prior art keywords
wax
polyvinyl alcohol
polyamine
coating
water
Prior art date
Application number
PCT/US2006/042149
Other languages
French (fr)
Inventor
Christopher B. Murphy
Jon O. Fabri
Original Assignee
Polymer Ventures, Inc.
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
Priority claimed from US11/259,491 external-priority patent/US7282273B2/en
Priority claimed from US11/478,018 external-priority patent/US20080003384A1/en
Application filed by Polymer Ventures, Inc. filed Critical Polymer Ventures, Inc.
Priority to CA002624983A priority Critical patent/CA2624983A1/en
Priority to EP06826967A priority patent/EP1940561A4/en
Publication of WO2007050964A1 publication Critical patent/WO2007050964A1/en

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/227Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of hydrocarbons, or reaction products thereof, e.g. afterhalogenated or sulfochlorinated
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions 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
    • C08L29/02Homopolymers or copolymers of unsaturated alcohols
    • C08L29/04Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L79/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
    • C08L79/02Polyamines
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • C08L91/06Waxes
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D129/00Coating compositions based on 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; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
    • C09D129/02Homopolymers or copolymers of unsaturated alcohols
    • C09D129/04Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D179/00Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen, with or without oxygen, or carbon only, not provided for in groups C09D161/00 - C09D177/00
    • C09D179/02Polyamines
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D191/00Coating compositions based on oils, fats or waxes; Coating compositions based on derivatives thereof
    • C09D191/06Waxes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/02Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with hydrocarbons
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/327Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof
    • D06M15/333Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated alcohols or esters thereof of vinyl acetate; Polyvinylalcohol
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/61Polyamines polyimines
    • 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
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/36Polyalkenyalcohols; Polyalkenylethers; Polyalkenylesters
    • 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
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/54Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
    • D21H17/56Polyamines; Polyimines; Polyester-imides
    • 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
    • D21H17/60Waxes
    • 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
    • D21H17/71Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
    • D21H17/72Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic material
    • 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
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/18Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising waxes
    • 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
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/20Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2203/00Other substrates
    • B05D2203/22Paper or cardboard
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/08Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain an anti-friction or anti-adhesive surface
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/03Polymer mixtures characterised by other features containing three or more polymers in a blend
    • 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
    • D21H19/00Coated paper; Coating material
    • D21H19/10Coatings without pigments
    • D21H19/14Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12
    • D21H19/24Coatings without pigments applied in a form other than the aqueous solution defined in group D21H19/12 comprising macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • D21H19/00Coated paper; Coating material
    • D21H19/80Paper comprising more than one coating
    • D21H19/82Paper comprising more than one coating superposed
    • D21H19/826Paper comprising more than one coating superposed two superposed coatings, the first applied being pigmented and the second applied being non-pigmented

Definitions

  • the present invention relates to methods to impart grease resistance and/or water resistance to materials, and more particularly to methods of improving grease resistance and/or water resistance that reduce or replace the use of fluorochemical compounds and involve two or more treatment agents.
  • ScotchgardTM® and Scotchban® contain fluorochemicals, which have recently become the object of health and environmental concerns because of their persistence and tendency to bioaccumulate. Consequently, there is strong interest in replacing or reducing the use of fluorochemical compounds such as perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), polytetrafluoroethylene (PTFE), perfluoro-n-decanoic acid (PFDA) and other perfluorinated compounds that are widely used for imparting grease, oil, and/or water resistance to the substrates to which they are applied.
  • PFOS perfluorooctane sulfonate
  • PFOA perfluorooctanoate
  • PTFE polytetrafluoroethylene
  • PFDA perfluoro-n-decanoic acid
  • Recently several products have been introduced into the marketplace as potential replacements for the fluorochemical compounds.
  • Waxes, coalescing solvents, and dyes are optionally included.
  • Polyvinyl alcohol has been widely used in films and coatings for properties that range from water dispersability to barrier properties. Examples of these uses are found in U.S. Patent Nos. 5,468,526, 5,110,390, 5,283,090, 6,113,978, US 2005/0042443 A1 , and GB 2 185 404A, among others.
  • U.S. Patent No. 5,981 ,011 to Overcash et a/ a coated sheet material is described that has as one component a barrier coating comprising a polymer mixture in which one polymer can be polyvinyl alcohol).
  • a cellulosic multi-ply paperboard that contains predominantly cellulosic fibers, a bulk and porosity enhancing additive, and a size press applied binder coating.
  • the paperboard can be coated with either a binder, such as polyvinyl alcohol), or with a wax.
  • a binder such as polyvinyl alcohol
  • a similar composition having a coating of either a binder such as polyvinyl alcohol) or a wax is described in U.S. Patent No. 6,379,497, to Sandstrom et al. [00008] In U.S. Patent No.
  • hinged starch- bound cellular matrix clam-shell type containers are described that can be coated on the interior with a wax coating.
  • the container can also be coated on the exterior with an elastomeric coating that can comprise polyvinyl alcohol) in order to strengthen the outer surface and reduce its tendency to fracture during the hinging action.
  • elastomeric coating can comprise polyvinyl alcohol
  • Similar articles produced from a starch-bound cellular matrix reinforced with dispersed fibers and having optional coatings of materials such as polyvinyl alcohol) or wax are discussed in U.S. Patent Nos. 5,660,900 and 5,683,772 to Andersen et al. [00009] Wenzel et al., in U.S. Patent Nos.
  • polyvinyl alcohol is described as being an ionically cross-linkable polymer that could be used in the invention, however, some carboxylate functionality must be added to the polymer prior to use by copolymerizing with a monomer having carboxylic acid pendant groups.
  • Other references have described the use of both waxes and substances such as polyvinyl alcohol) for various purposes, in particular in the field of surface preparations for paper and textiles.
  • U.S. Patent No. 5,151,404 to Suzuki et al. describes thermosensitive recording paper that does not curl and provides clear images with high image density.
  • paraffin wax can be used as a sizing agent in the paper
  • polyvinyl alcohol can be used as a stiffness-imparting agent.
  • U.S. Patent No. 5,763,100 to Quick etal. describes recyclable acrylic coated papers that have water and grease resistance and limited moisture vapor transmission characteristics.
  • the papers can have a primer coat, which is commonly a water-based dispersion of a polymer such as polyvinyl alcohol), and a further coating of a water-based emulsion of an acrylic-styrene copolymer and a wax, which can be a paraffin wax.
  • a supple biodegradable sheet that is resistant to bursting and has poor water and other liquid absorbing power.
  • the sheet comprises fibers, an optional moisture resisting agent, a binder, which can be polyvinyl alcohol), a moisture retaining agent, and a sizing agent, which can be a paraffin wax.
  • Dettling in U.S. Patent No. 5,773,131 , describes a paper product having a flavor seal and a vapor barrier that is produced by applying a primer coating to the paper that can include polyvinyl alcohol), and after polymerizing the coating to form an amorphous net structure, applying a cover coating mixture suitable for generating a vapor seal.
  • the cover coating mixture can include paraffin wax.
  • Dragner et ai in U.S. Patent No. 5,795,932, describe a surface sizing composition for nonwoven substrates that includes a waxy material, that can be a paraffin wax, but is preferably a stearylated melamine, and a surfactantless vinyl polymer or copolymer emulsion that contains an alkali soluble, acid containing copolymer, which acts as the only surfactant for the waxy material.
  • a waxy material that can be a paraffin wax, but is preferably a stearylated melamine
  • a surfactantless vinyl polymer or copolymer emulsion that contains an alkali soluble, acid containing copolymer, which acts as the only surfactant for the waxy material.
  • the sheets can be coated with various materials, selected to improve water penetration, or grease and oil penetration, or to render the article substantially liquid-tight, or pressure- tight, or to increase the flexibility of the article, and polyvinyl alcohol) and waxes are included in a list of several possible coating materials. It is stated that mixtures of the coating materials can also be used, but no particular mixture is identified as being preferred. Methods for the production of articles of a similar nature are described by Andersen et a/, in U.S. Patent Nos. 5,580,409 and 5,800,647.
  • the films are said to provide an effective moisture and oxygen barrier without requiring such barrier agents as polyterpenes, alicyclic hydrocarbons, or high barrier polyvinylidene chloride coatings.
  • the films include a layer comprising an olefin polymer, and a barrier layer comprising a syndiotactic polypropylene homopolymer and a wax. They can further include an outer layer that can be coated, for example, with a polyvinyl alcohol) coating.
  • Chang et a/ describe a method of making a flushable film having barrier properties in U.S. Patent No. 6,479,105.
  • the film can have a water-dispersible substrate layer that can comprise polyvinyl alcohol) that is covered with a coating of a low molecular weight amorphous poly(alpha- olefin) that can be admixed with a branched paraffin wax.
  • a formulation for providing oil and grease resistance and release paper properties is described as including a fatty acid melamine and paraffin wax emulsion and a polyvinyl alcohol).
  • the formulation can include a fatty acid melamine wax and a polyvinyl alcohol).
  • a preferred fatty acid melamine wax is a stearylated melamine wax.
  • the formulation can be used as a coating to provide oil and grease resistance on paper and paperboard, and can also be applied inline on a paper machine.
  • the present invention is directed to a novel method of improving grease and/or water resistance of a material, the method comprising treating the material with wax and polyvinyl alcohol).
  • the present invention is also directed to a novel composition for improving grease and/or water resistance of a material, the composition comprising wax and polyvinyl alcohol).
  • the present invention is also directed to a novel material that has been treated with a composition comprising polyvinyl alcohol) and wax.
  • the present invention is also directed to a novel material that has been treated with polyvinyl alcohol), wax and a polyamine.
  • the present invention is also directed to a novel method of improving the gas, water, water vapor, or grease resistance of a porous material, the method comprising: applying to the porous material a first treatment agent; and after the first treatment agent has been applied to the porous material, applying to a surface of the porous material wax, polyvinyl alcohol), and optionally a polyamine, thereby improving the gas, water, water vapor, or grease resistance of the porous material.
  • the present invention is also directed to a novel porous material having improved gas, water, water vapor and/or grease resistance comprising the porous material having a surface on which is a first coating of a first treatment agent and a second coating comprising wax, polyvinyl alcohol) and optionally a polyamine over the first coating.
  • the present invention is also directed to a novel porous material that has been treated by the method described above.
  • treatment with a combination of paraffin wax and polyvinyl alcohol provided protection levels of Kit number 4, even at a dosage as low as 0.156 Ib d.s./3000 ft 2 , and protection of Kit number 5 at 0.468 lbs d.s./3000 ft 2 , and Kit number 6 at 0.624 lbs d.s./3000 ft 2 .
  • the intent of the invention is that the first treatment step is an optional step, and the first treatment agent is an optional agent. Accordingly, as used herein, reference to the second treatment step, second treatment agent, and/or the second coating will be understood as being the only treatment step or coating when the first treatment step or coating is absent in accordance with the intent of the invention.
  • a commercial coating of a polymer latex and filler provided grease resistance (reported as Kit numbers measured according to TAPPI TEST METHOD T-559 "Grease Resistance for Paper and Paperboard") of about zero (0), but treatment of the coated whiteboard with a wax/poly(vinyl alcohol)/polyamine coating, even at dosage rates of under 10 lbs.
  • Another feature of the present invention is that such superior performance can be obtained without the use of higher, and more expensive, grades of polyvinyl alcohol). It has been shown that the present methods can be carried out successfully with less expensive grades of polyvinyl alcohol), such as partially hydrolyzed and intermediate hydrolyzed polyvinyl alcohol), and that the use of higher grades, such as fully hydrolyzed or super hydrolyzed, is not required. This feature is highly advantageous in controlling the expense of the coating procedure, and improves the cost effectiveness of the innovative method.
  • the inventors have found that the addition of a polyamine to the combination of wax and polyvinyl alcohol) provides additional improvement in the performance of the compositions.
  • a combination of paraffin wax, polyvinyl alcohol), and dicyandiamide-formaldehyde condensate provided protection levels of Kit number 7 at dosage rates of 0.468 lbs d.s./3000 ft 2 .
  • the present specification refers to an improvement in the gas, water, water vapor, and/or grease resistance of a porous material, what is meant is any increase, no matter how small, in the resistance of the porous material to penetration by any type of gas, water, water vapor and/or grease.
  • grey refers to any type of oil, fat, or lipid, whether natural or synthetic, and includes without limitation, natural fats and oils, such as seed oils, including corn oil, soybean oil, rapeseed oil, sunflower oil, and the like, lard, animal fats, and synthetic oils, such as silicone oil and the like, and also liquid, semi-solid and solid hydrocarbons.
  • natural fats and oils such as seed oils, including corn oil, soybean oil, rapeseed oil, sunflower oil, and the like, lard, animal fats, and synthetic oils, such as silicone oil and the like, and also liquid, semi-solid and solid hydrocarbons.
  • improving the gas, water, water vapor, or grease resistance of the porous material comprises increasing the grease resistance of the porous material as measured by Kit number, where the wax, polyvinyl alcohol) and optional polyamine are applied in an amount sufficient to improve the grease resistance by at least 3 Kit numbers.
  • improving the gas, water, water vapor, or grease resistance of the porous material comprises increasing the grease resistance of the porous material as measured by Kit number, where the wax, polyvinyl alcohol) and optional polyamine are applied in an amount sufficient to improve the grease resistance by at least a factor of 2 but no less than 2 Kit numbers.
  • a coating of the first treatment agent can be applied by adding the first treatment agent to the wet end of a paper machine.
  • the first treatment agent therefore, is distributed throughout the depth of the paper, but such application is still embraced by the term “coating”, as used herein.
  • the terms “surface coating” are meant to refer to a coating that is applied to the outer surface of a porous material, such as a spray or roll coating applied to a dry paper web.
  • the first treatment agent can be any treatment agent that is know for use in sizing, increasing water resistance, gas resistance, water vapor resistance, wet strength, dry strength, softness, drape, hand, and/or the printability of a porous material, except those agents that are not compatible with a subsequent treatment comprising wax and polyvinyl alcohol), optionally with a polyamine.
  • the first treatment agent can be applied during the formation or manufacture of the porous material, such as at the wet end of a paper machine. Preferably, however, the first treatment agent is applied to a surface of the porous material after the material has been formed. An example of this is the application of the first treatment agent as a coating on paper at the dry end of the paper machine, or at any time after formation of the paper web.
  • the first treatment agent can be provided in the form of a waterborne coating formulation or a solventborne coating formulation.
  • the first treatment agent comprises a polymer binder.
  • the polymer can be applied neat, as in a hot melt roll application (such as is used for the application of a polyethylene wax to paperboard for the manufacture of milk cartons), or it can be applied as a solution or in a dispersion as a latex. It is common that the polymer is dispersed as a waterborne latex due to the low toxicity, safety and low organic emissions of the application process.
  • polymers that are useful as the polymer binder of the first treatment agent include polyvinyl alcohol), polyacrylate, polystyrene/polyacrylic copolymer, cellulose derivative, nitrocellulose, vinyl chloride, vinyl chloride copolymers, vinyl acrylate copolymers, vinyl acetate homopolymers, vinyl acetate copolymers, styrene butadiene polymers, styrene butadiene acrylonitrile polymers, polyvinylacetate, proteins, milk proteins, starch, and mixtures of any of these.
  • the first treatment agent can include wax, polyvinyl alcohol) and optionally a polyamine. In other words, it can be the same as, or similar to the composition that is used in the subsequent wax/poly(vinyl alcohol) and optional polyamine treatment.
  • the first treatment agent can have additional components and common additional components can include pigments, such as natural or synthetic pigments; minerals, such as calcium carbonate, titanium dioxide, Kaolin clay, Montmorillionite clay, and gypsum; organic opacifiers; lubricants; surface sizes, such as starch; saturants; release coatings; rheology modifiers; dispersants; insolubilizers; or plasticizers, such as dioctyl phthalate, tricresyl phosphate, and castor oil.
  • the first treatment agent can include any of these materials and any mixtures thereof.
  • latex binders with inorganic fillers, as described above, are preferred.
  • the first treatment agent is applied in any amount that will achieve the beneficial effects described above. However, in some embodiments, it is preferred that the first treatment agent is applied in an amount of from about 0.1 to about 50 g/m 2 . It is more preferred that the amount of the first treatment agent to be applied is from about 1 to about 30 g/m 2 , and an amount of from about 2 to about 20 g/m 2 is even more preferred.
  • the first treatment agent may be used as many commercially available materials. These include products marketed under the tradenames of RHOPLEX, POLYCO, ROPAQUE, ACUMER and TAMOL, all available from RohmNova, Mogadore, OH. [00046] It should be noted that the present invention embraces the embodiment where the step of applying the first treatment agent is done by another. In other words, the first step of applying the first treatment agent is intended to embrace the act of selecting a pre-coated porous material, to which one can then apply the wax/poly(vinyl alcohol) and optional polyamine.
  • the present invention offers an advantage of providing superior water and grease resistance with the use of coatings that are free of fluorochemical compounds
  • the invention also embraces the situation where a reduced amount of a typical fluorochemical water, oil and/or grease proofing agent, such as perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), polytetrafluoroethylene (PTFE), perfluoro-n- decanoic acid (PFDA), or the like, is used in conjunction with the present method to obtain superior Kit numbers.
  • PFOS perfluorooctane sulfonate
  • PFOA perfluorooctanoate
  • PTFE polytetrafluoroethylene
  • PFDA perfluoro-n- decanoic acid
  • the conventional fluorochemical agent can be applied prior to the present method, or is optionally applied as the first treatment agent, and the second treatment agent is then applied to provide superior levels of grease and/or oil and water resistance.
  • a reduced amount of a typical fluorochemical agent it is meant that at least 10% less of the fluorochemical agent is used than would otherwise be required to obtain the Kit number that is achieved when the fluorochemical agent is used in conjunction with the present method.
  • the amount of the fluorochemical agent is 25% less, more preferably 50% less than would be required without the use of the novel method.
  • any suitable polyvinyl alcohol can be used in the present methods and compositions.
  • Polyvinyl alcohol is a polymer comprising vinyl acetate monomer units, some of which have been hydrolyzed to yield alcohol functional groups on the polymer.
  • Polyvinyl acetate) and polyvinyl acetate-co-vinyl alcohol are also included in the definition of polyvinyl alcohol).
  • the polymer can contain other co-monomers such as ethylene, propylene, butylene, ethylene oxide, propylene oxide, and the like without departing from the scope of the invention.
  • the polyvinyl alcohol can be in the physical form of a solid, an emulsion, a suspension, or a liquid solution.
  • polyvinyl alcohol The physical properties of polyvinyl alcohol are controlled by molecular weight and the degree of hydrolysis, and a wide range of commercial grades is offered by polyvinyl alcohol) manufacturers. Some of the commercially available grades of polyvinyl alcohol) are: Partially Hydrolyzed, Intermediate Hydrolyzed, Fully Hydrolyzed, and Super Hydrolyzed. The molecular weight depends on the conditions of polymerization, and the degree of hydrolysis is defined as the percent of acetate groups replaced by hydroxyl groups during the hydrolysis reaction. The specific gravity of polyvinyl alcohol) solutions depends on concentration and temperature and is independent of grade. Polyvinyl alcohol) reacts in a manner similar to secondary alcohols.
  • the polyvinyl alcohol) employed in accordance with this invention may be any grade polyvinyl alcohol) that is compatible with paraffin waxes and optionally with polyamines such as dicyandiamide- formaldehyde condensate and that provides improved grease resistance or improved water resistance, or both, when applied to a material, such as paper, in combination with paraffin wax and optionally a polyamine.
  • the polyvinyl alcohol) component comprises a partially hydrolyzed polyvinyl alcohol), typically having a percent hydrolysis of about 87% - 89% and a viscosity of about 45 - 55 centipoise (4% aqueous solution at 2O 0 C).
  • polyvinyl alcohol The manufacture of polyvinyl alcohol involves starting with polyvinyl acetate and converting that material to polyvinyl alcohol) generally by base-catalyzed methanolysis.
  • Polyvinyl acetate polymerization is done by conventional processes such as, for example, solution, bulk or emulsion polymerization.
  • the polymerization step controls the ultimate molecular weight of the polyvinyl alcohol).
  • Catalyst selection, temperature and solvent control the degree of polymerization.
  • the degree of hydrolysis of polyvinyl alcohol is controlled during the alcoholysis reaction and is independent of molecular-weight control. Fully hydrolyzed polyvinyl alcohol) is obtained if methanolysis is allowed to go to completion.
  • the reaction can be terminated by neutralizing or removing the sodium hydroxide catalyst.
  • the addition of small amounts of water to the reactants promotes saponification of polyvinyl acetate, which consumes sodium hydroxide.
  • the extent of hydrolysis is inversely proportional to the amount of water added. Typical degrees of hydrolysis of commercial grades of polyvinyl alcohol) are: Super Hydrolyzed (over 99.3%), Fully Hydrolyzed (98.0 - 98.8%), Intermediate Hydrolyzed (91.0 - 96.5%, with range varying by molecular weight), and Partially Hydrolyzed (86.0 - 89.0, with range varying by molecular weight).
  • polyvinyl alcohol which is partially hydrolyzed and which is suitable for use in the present invention
  • Celvol 840 which is available from Celanese Corporation of Dallas, TX.
  • the polyvinyl alcohol) can be used neat, or it can be used in combination with a defoamer. It is not uncommon to add a defoamer when using an intermediate or partially hydrolyzed grade or polyvinyl alcohol).
  • Any wax can be used in the methods and compositions of the present invention.
  • Useful waxes may be natural or synthetic, or combinations thereof, and may be macrocrystalline or microcrystalline.
  • the wax can be obtained from animal, vegetable or mineral sources, or it may be produced synthetically.
  • Useful waxes generally have melting points within the range of about 20 0 C to about 200 0 C, and include animal waxes, mineral waxes, vegetable waxes, insect waxes, and synthetic waxes including: beeswax; bayberry-myrtle; candelilla; caranday; carnauba; castor bean wax; esparto grass wax; Japan wax; montan crude wax; ouricury; retamo-ceri nimbi; shellac wax; spermaceti; sugar cane wax; and wool wax-lanolin.
  • Paraffins and chlorinated paraffin waxes also are of interest as the wax components of the present methods and compositions, as are waxes produced by the emulsion polymerization of ethylene, styrene, or acrylates (weight average molecular weights of about 10,000 to about 50,000).
  • Oxidized hydrocarbon waxes such as those manufactured from the Fisher-Tropsch paraffins, and the microcrystalline petroleum waxes (ester- type waxes) also are useful in the methods and compositions of the present invention.
  • Other synthetic waxes of entirely different structure such as the fatty amides, imides, amines, and nitrites can be waxlike and can be used in the present invention.
  • the polyoxyethylenes or carbowaxes are an important group of waxes because of their solubility properties and compatibility with fatty materials.
  • the petroleum waxes particularly paraffin waxes but also the microcrystalline waxes are particularly preferred for use in the present invention.
  • the petroleum waxes are predominantly long chain (Ci 6 -C 50 ) alkane compounds.
  • the paraffins are mostly straight-chain molecules, but may have branched claims.
  • the microcrystalline waxes range in molecular weight from about 400 to about 700 and have average molecules of about 40 to about 50 carbon atoms.
  • the microcrystalline waxes have more branched-chain molecules than in paraffin waxes, containing an average of three carbon atoms per side chain. Oxidized microcrystalline waxes also are useful in the compositions of the present invention.
  • Petroleum waxes contain both solid and liquid hydrocarbons with the liquid hydrocarbons held in discrete droplets within the petroleum wax.
  • the paraffin waxes used in the compositions of the present invention may be crude scale wax and/or fully refined wax.
  • Synthetic paraffin waxes are mixtures of saturated straight-chain paraffinic hydrocarbons with short side chains (C 1 - C 4 ).
  • the weight average molecular weight is about 700 to about 800 or about 45-60 carbon atoms per molecule.
  • Paraffin wax is a preferred wax for use in the present invention. Any type or grade of paraffin wax can be used in the present invention that is compatible with polyvinyl alcohol) and optionally with a polyamine, and that provides improved resistance to grease or improved resistance to water, or both, when applied to a material such as paper in combination with polyvinyl alcohol) and optionally with a polyamine such as dicyandiamide-formaldehyde condensate.
  • Preferred paraffin waxes are unbranched or sparsely branched waxy white or colorless solid hydrocarbon mixtures that can be used to make candles, wax paper, lubricants, and sealing materials.
  • the chemical composition of a preferred paraffin wax is a mixture of predominantly non- aromatic saturated hydrocarbons with the general formula C n H( 2n + 2 ) where n is preferably an integer between 12 and 50, and more preferably between 22 and 27. It is preferable that the paraffin has a melting point, or melting point range, between about 25°C and about 200° C, more preferably between about 47°C and 95°C, and yet more preferably between about 47°C and abut 65°C, and is insoluble in water.
  • paraffin wax is available from Sigma-Aldrich, Milwaukee, Wl, as Cat. No. 31 ,765-9, having a CAS RN of 8002-74-2, and a melting point range of 52° - 58°C.
  • Other organic materials can be used with, or added to, the wax without departing from the scope of the invention.
  • the wax when it is to be used as an aqueous emulsion, it is common to add an emulsifier to the mixture to stabilize the emulsion.
  • a commonly used emulsifier for this purpose is a styrene-acrylate copolymer.
  • Another commonly used material is Morez 101 (a butyl acrylate methyl- methacrylate copolymer available from Rohm & Haas).
  • the wax, water, and the emulsifier can be intermixed with high shear to form a stable emulsion, which can then be used in suitable amounts to produce the compositions of the present invention.
  • paraffin wax and polyvinyl alcohol be the only materials present that have a significant effect on the grease and/or water resistance of the material. This is advantageous in circumstances where it is desirable to limit the cost or complexity of the treatment.
  • the treatment and compositions are said to consist essentially of polyvinyl alcohol) and paraffin wax.
  • a polyamine can be included as a component of the wax/poly(vinyl alcohol)/polyamine coating.
  • the preferred polyamine is an amine-aldehyde condensate that is the reaction product of an amine containing an active hydrogen atom and an aldehyde.
  • the amine include guanidine, urea, dicyandiamide, melamine, aniline, ethylenediamine, diethylenetriamine, monoethanolamine, diethanolamine, polyoxyalkyleneamines, polyoxyalkylenediamines, polyoxyalkylenetriamines, and the like.
  • aldehyde examples include formaldehyde, acetaldehyde, glutaraldehyde, glyoxal, hexamethylenetetramine, and paraformaldehyde.
  • examples of polyamines that are useful in the present invention include a condensation product of any one or more of the amines listed above with any one or more of the aldehydes listed above.
  • Polyamines that are useful in the present invention also include, without limitation, polyoxyalkyleneamines, polyoxyalkylenediamines, polyoxyalkylenetriamines, and mixtures of any of these. Examples of these materials include the Jeffamine® series of polyoxyalkyleneamines available from Huntsman Corporation, The Woodlands, TX.
  • the reaction between the amine and aldehyde is usually conducted in aqueous solution and can be done at acid, neutral, or alkaline pH.
  • the preferred condition is acid pH. Additional information regarding the production of suitable dicyandiamide-formaldehyde condensates can be found, for example, in U.S. Patent 3,957,574 to Anderson.
  • a preferred polyamine for the present invention is a dicyandiamide-formaldehyde condensate.
  • Examples of polyamines that are considered to be dicyandiamide-formaldehyde condensates, and which are useful in the invention are available from Polymer Ventures, Inc., Charleston, SC, as RD111-013 and PC-540.
  • RD111-013 is an acid condensation product of dicyandiamide, urea, and formaldehyde, and is available as a clear viscous solution of 46% d.s. having a viscosity of 50 - 250 cps and a pH of about 5.5. It is cationic and has a density of about 10 lbs/gal.
  • PC-540 is an acid condensation product of dicyandiamide, urea, and formaldehyde and is available as a clear viscous solution of 50% d.s. having a viscosity of 10 - 100 cps and a pH of about 3.5. It is cationic and has a density of about 10 lbs/gal. Either of these polyamines can be used as commercially supplied.
  • the first treatment agent or the second coating include only polyvinyl alcohol) and wax as the penetration-resistance controlling agents
  • the two components can be used in any amounts.
  • the ratio of the polyvinyl alcohol) to the wax, by weight is within a range of about 10:90 to about 90:10, a range of about 25:75 to about 75:25 is more preferred, a range of about 40:60 to about 60:40 is even more preferred, and a range of about 45:55 to about 55:45 is yet more preferred.
  • about 44% polyvinyl alcohol) and about 56% wax, by weight has been found to provide improved resistance.
  • the polyvinyl alcohol), the wax, and the polyamine can each be included in almost any relative amount.
  • the three components be used in combinations in which the polyvinyl alcohol) is within a range of about 3 to about 74 % by wt. d.s. (where the dry solids (d.s.) include only the three components of interest), the wax is within a range of about 13 - 96 % by wt. d.s., and the polyamine is within a range of about 0.5 - 13 % by wt. d.s.
  • the three components be used in combinations in which the polyvinyl alcohol) is within a range of about 22 to about 68 % by wt. d.s., the wax is within a range of about 25 - 74 % by wt. d.s., and the polyamine is within a range of about 3 - 12 % by wt. d.s. It is even more preferred that the three components be used in combinations in which the polyvinyl alcohol) is within a range of about 38 to about 68 % by wt. d.s., the wax is within a range of about 25 - 55 % by wt.
  • the polyamine is within a range of about 6 - 12 % by wt. d.s.
  • the present methods and compositions can be achieved with combinations of polyvinyl alcohol), wax, and polyamine having a weight ratio of the three components, respectively, of about 4/5/1 , or 5/4/1 , or 4.5/4.5/1.
  • the polyvinyl alcohol) and the wax, and optionally the polyamine can be intermixed into a composition that can be applied to the porous material to be treated.
  • the components can be applied separately. If the components are administered separately, they can be administered at approximately the same time, or they can be administered at different times.
  • separate solutions or emulsions of each component can be administered to the material to be treated, or the solutions or emulsions can be intermixed and then applied to the material as a single composition.
  • the polyvinyl alcohol), wax, and optionally, the polyamine, of the present invention can be present in the solutions, suspensions, dispersions, or emulsions, or in the compositions of the invention, in almost any concentration. It is preferred that the present compositions contain from about 0.5% to about 60% by weight dry substance, based only on the polyvinyl alcohol), wax, and polyamine, more preferred that they contain from about 1 % to about 50% by wt. d.s., and even more preferred that they contain from about 20% to about 40% by wt. d.s. The present compositions can be diluted prior to use, and after dilution, a d.s.
  • the wax/poly(vinyl alcohol) and optionally polyamine are applied in a sufficient amount so as to provide the level of performance desired, and that amount may vary widely according to the porous material and its characteristics, such as porosity and surface roughness, as well as the type and amount of the first treatment agent when one is used.
  • the rheological characteristics of the wax/PVOH/optional polyamine coating composition, such as viscosity can also have an affect.
  • wax/PVOH/optional polyamine compositions are applied to sheet material having a measurable surface area, such as paper, for example, typical use rates for the present invention, whether only polyvinyl alcohol) and wax are used, or when a polyamine is also included, range from about 0.1 to about 4 lbs dry solids (d.s.) per 3000 ft 2 of surface of the material to be treated.
  • the components be applied at a rate of between about 0.1 and about 3 lbs d.s./3000 ft 2 , even more preferred is an application rate of between about 0.15 to about 2.0 lbs d.s./3000 ft 2 , more preferred is an application rate of between about 0.15 and 1.0 lbs d.s./3000 ft 2 , and yet more preferred is an application rate of between about 0.4 and 1.0 lbs d.s./3000 ft 2 .
  • materials other than the polyvinyl alcohol), wax, and optional polyamine can be used in the second treatment along with these ingredients without departing from the scope of the invention. It has been shown, for example, that it is often desirable to add an emulsifier along with the wax in order to form a stable aqueous emulsion. Other materials, such as colorants, dyes, preservatives, anti-fungal agents, surfactants, and the like, can also be used along with the wax, polyvinyl alcohol) and optional polyamine in the present method. [00079] Although it is possible, and even desirable, to provide and use the wax, the polyvinyl alcohol) and the optional polyamine in aqueous solutions or emulsions, that is not required. In certain circumstances, for example, it might be useful to provide one or more of the components in an organic solvent, or in a molten form, or even in a dry form, such as a powder or flake.
  • compositions of the present invention can be used to treat materials of any sort that would benefit from an improvement in resistance to grease, or resistance to water, or both.
  • the components of the present methods can be applied as coatings or in any other fashion at any point during the manufacture, packaging, storage, or use of the material to be treated.
  • packaging and non-packaging materials such as paper, cardboard, bakery board, butter and margarine chips, candy board, cup stock, frozen food containers, plate stock, artist's papers, asphalt laminations, carbonizing tissue, carton overwraps, cover and text papers, envelopes, garbage and trash bags, label papers, paper placemats, release papers, soap containers, wallpaper, liner board, folding cartons, multiwall bags, flexible packaging, duplicator and reproduction papers, support cards and medical dressings.
  • present methods and compositions can be used to improve grease, oil, and moisture resistance of asphalt, wood, textile fabric, such as woven and non-woven fabrics, yarn, thread, carpets, upholstery, paperboard, formed articles, medical dressings, and the like.
  • Present materials to be treated are porous, and therefore not impervious to gas, water, water vapor and grease, although such resistance may vary widely.
  • the present porous materials are commonly in sheet form and include substrates comprised of non-woven and woven polymers such as fabrics, and cellulose-based materials, such as paper and cardboard substrates, and the like.
  • sheet material refer to a material in a form that has length and width dimensions that are each significantly greater than the thickness of the material.
  • sheet materials include paper, paperboard, housewrap, tarpaper, and the like.
  • the amount of sheet materials can often be characterized in terms of surface area, and the dosage rate of material that is added to a sheet material can be expressed on the basis of the surface area of the material.
  • An example of this type of measurement is a dosage rate expressed as lbs per ft 2 , or pounds per unit area.
  • the paper comprises a porous sheet material made of a cellulosic material, or a cellulose-based material.
  • Such paper sheet materials include, for example, corrugated paperboard (or "cardboard"), newsprint paper, uncorrugated Kraft paper stock, pan liner paper stock, and the like.
  • other cellulose-based sheet materials such as pressed board, may also be suitable. It is also possible to use other fibrous materials for the substrate sheet material.
  • the present invention can be used to improve the grease and/or water resistance of paper.
  • the first treatment agent alone or along with the first treatment agent and the wax/poly(vinyl alcohol) and optional polyamine can be added to the wet end of a typical Fourdrinier machine, or they can be used to coat paper after it has been dried.
  • the first treatment agent can be added to the wet end of a paper machine and the wax/poly(vinyl alcohol) and optional polyamine can be added as a coating to the paper at the dry end of the machine.
  • the first treatment agent and/or the wax/poly(vinyl alcohol) and optional polyamine are used as a coating, particularly on paper
  • the components may be applied as a solution, emulsion, or dispersion, by roll coater, brush, doctor blade or blade coater, sprayer or other such suitable application means.
  • the coated materials are dried after the wax/poly(vinyl alcohol) and optional polyamine has been applied.
  • further coatings or treatments may be applied to the material.
  • Such coatings could include heat shielding coatings, UV-resistant coatings, coatings with specific chemical resistance, or the like.
  • the coated material may be formed into a shaped article by means other than folding and gluing, such as, for example, by pressure- forming.
  • Such shaped articles may be used for cooking or baking purposes.
  • the coated material may be used to make a container for storing food on a shelf (such as for storing pet food) while preventing penetration of grease, oil and/or water through the material.
  • the coated material may be used to form a container such as a baking tray.
  • the coated material may be used to form a food receptacle such as a paper plate.
  • the coated material may be used for fast-food containers, such as boxes for fried chicken, or food wrappers, such as wrapping materials for hamburgers and sandwiches.
  • the coated material may be used for any of a variety of applications as a food container, wrapper or receptacle.
  • This example shows the preparation, application and efficacy of compositions containing wax and polyvinyl alcohol and optionally a polyamine as coatings for paper.
  • Paper sheets were supplied from a paper mill in Wisconsin. The sheets were production run non- coated paper having a basis weight of 20 and 20.5 pounds per 3000 square feet. [00092] Sheets were coated with a Gardco automated drawdown machine (available from Paul N. Gardner Company, Inc., Pompano Beach, FL) running at 1.5 cm/ second, using various drawdown rod sizes to give coat weights ranging from 0.05 to 2 dry pounds / 3000 square feet. [00093] Grease resistance tests were conducted in accordance with TAPPI TEST METHOD T-559 "Grease Resistance for Paper and Paperboard"
  • compositions A, B, and C were made up as aqueous solutions or emulsions with the various components of the present compositions.
  • Composition A Polyvinyl alcohol
  • Distilled water 450 g was added to a 1 -liter glass reaction flask fitted with a condenser, and temperature probe. Agitation was started using an overhead mixer and a glass rod fitted with a half moon mixing blade.
  • Celvol 840 50 g
  • PVOH partially hydrolyzed polyvinyl alcohol
  • Composition B solution of polyfvinyl alcohol and polyamine in water
  • Distilled water 439.5 g was added to a 1 -liter glass reaction flask fitted with a condenser, and temperature probe. Agitation was started using an overhead mixer and a glass rod fitted with a half moon mixing blade. Then 15.5 g of a 50% active urea-dicyandiamide- formaldehyde copolymer (polyamine) was added. Celvol 840 (45 g) was slowly poured into the vortex to ensure full wetting of the PVOH particles. The temperature was then increased to 85-90°C and the solution was allowed to cook for 1 hour until the PVOH was fully dissolved.
  • Composition C emulsion of paraffin wax in water with styrene-acrylate copolymer as an emulsion stabilizer
  • a lab homogenizer (Ultra Turrax T25 from IKA Works, Inc.) was the placed in the reactor and the reactor was allowed to cool to ⁇ 60°C. At 6O 0 C the homogenizer was turned on at 24,000 rpm for several minutes.
  • Compositions D - J mixturetures of wax and PVOH and optionally with polvamine
  • Compositions D-J where made in accordance with the relative amounts of components as shown in Table 1.
  • the appropriate amount of Composition A or Composition B was placed in a 500ml beaker fitted with an over head mixing shaft, and the appropriate amount of Example C was slowly added with agitation until the blend was smooth.
  • Table 2 shows the amounts of each of the three ingredients in each of Compositions A - J in terms of the percent by weight of the component relative to the dry weight of the to;tal amounts of wax, polyvinyl alcohol) and urea-dicyandiamide- formaldehyde copolymer condensate in the composition. Accordingly, any amount of other materials, such as emulsifiers, and the like, are not reflected in the calculation shown in Table 2.
  • Table 1 Grease and water resistance-improving compositions of the present invention having various relative amounts of polyvinyl alcohol) and wax.
  • Table 2 Relative amounts of components in the compositions of Table 1 in terms of percent dry weight.
  • PVOH polyvinyl alcohol
  • Celvol 840 from Celanese Corporation.
  • Wax is paraffin wax having a melting point of 52° - 58°C from Sigma-Aldrich.
  • Polyamine is dicyandiamide-formaldehyde condensate.
  • d) (% by wt. d.s.) means the percent of the component relative to the total amount of PVOH, Wax, and Polyamine.
  • Table 3 Kit numbers for grease resistance and water repellency for paper treated with the compositions shown in Tables 1 and 2. Dosage rates were determined by the use of different drawdown rods and the base paper was 20 - 20.5 lb/3000 ft 2 basis weight.
  • compositions A, B, and C alone as a coating at various dosages add little to no grease/oil resistance to the paper substrate.
  • the highest Kit number obtained was 3.
  • Composition A PVOH
  • Composition C paraffin wax
  • a noted increase in Kit number is observed (Kit number 2-3 up to Kit number 5-6), even at the same total dosage of solids.
  • the incorporation of the polyamine into the combination with polyvinyl alcohol) and wax (noted as Composition F), but at the same level of solids dosage, further increases the Kit number to 6-7.
  • the results for Compositions D-I show that an optimum in grease/ oil resistance is established with the blending of the paraffin wax to the polyvinyl alcohol)/polyamine blend, as indicated by the data in Tables 2 and 3.
  • the uncoated sheet resulted in a water drop diameter of 12 mm compared to a range of 7 - 8 mm for the treated samples. Furthermore, the uncoated sheet resulted in the water spreading over time and soaking into the sheet, whereas the sheets coated with Compositions D - I 1 as well as Composition C, showed smaller water drop diameters, thus indicating improved water repellency, and showed no drop spreading over time and no soaking in of the water drop. Paper coated with Compositions A and B showed slightly improved water repellency over the control, however there was some droplet spread over time, but the drops did not soak into the sheets.
  • the coated paperboard had been commercially coated with a polymer latex binder/filler formulation prior to the application of the wax/PVOH/polyamine coating.
  • the wax/PVOH/polyamine coating comprised 38.4% polyvinyl alcohol) Celvol 840, from Celanese Corporation, 54.9% paraffin wax having a melting point of 52° - 58 0 C from Sigma-Aldrich, and 6.6% dicyandiamide-formaldehyde condensate as the polyamine (all percentages are on a percent of dry matter basis).
  • the components were dispersed in distilled water and applied to the paperboard at a solids concentration of 6% or 8%. Films of several different thicknesses were used.
  • the method of coating and drying was the same as described above in Example 1 , as was the method of measuring grease resistance (Kit Number).
  • Table 4 shows film thicknesses, product application rates and Kit Numbers resulting from coatings placed on uncoated (1 - 8) and coated (9 - 12) paperboard.
  • Table 4 Grease resistance of 190# white paperboard with and without a latex polymer/filler precoat and with different application rates of a wax/PVOH/polyamine second coating.
  • a This refers to the number of pounds of a formulation of the wax/PVOH/polyamine coating at 23% solids in water that was applied per ton of dry paper. That formulation was diluted further prior to application with water to 6% solids for tests 1 - 6 and 9 - 12 and to 8% solids for tests 7 and 8.
  • OUN refers to uncoated paperboard with no wax/PVOH/polyamine coating
  • OCO refers to coated paperboard with no wax/PVOH/polyamine coating.
  • the grease resistance of the board increased significantly in a dose-responsive manner up to a Kit number12 at a coating rate of about 19.8 lbs dry solids/ton of paper of the wax/PVOH/polyamine coating (about 85 lbs of the 23% actives formulation/ton of paper).

Abstract

A method of improving gas, water, water vapor, and/or grease resistance of a porous material is disclosed which comprises treating the material with a wax, poly(vinyl alcohol), and optionally a polyamine. In some embodiments, an optional first treatment agent may be applied to the material prior to the application of wax and poly(vinyl alcohol) and optionally a polyamine. Materials that have a single coating of wax, poly(vinyl alcohol), and optionally a polyamine, as well as materials having a multi-layer coating that includes a first coating of a first treatment agent and a second coating of wax, poly(vinyl alcohol), and optionally a polyamine are also disclosed.

Description

GREASE AND WATER RESISTANT ARTICLE
BACKGROUND OF THE INVENTION
(1) Field of the Invention:
[00001] The present invention relates to methods to impart grease resistance and/or water resistance to materials, and more particularly to methods of improving grease resistance and/or water resistance that reduce or replace the use of fluorochemical compounds and involve two or more treatment agents.
(2) Description of the Related Art:
[00002] Materials, such as paper and textiles, are commonly treated or coated to improve their resistance to liquids such as water, grease and oil. Commercial compounds such as ScotchgardTM® and Scotchban®, both products of Minnesota Mining and Manufacturing Co. have been widely used to improve the barrier properties of papers, textile fabrics, nonwoven fabrics, upholstery, carpet fibers, and the like.
[00003] ScotchgardTM® and Scotchban®, and similar products, contain fluorochemicals, which have recently become the object of health and environmental concerns because of their persistence and tendency to bioaccumulate. Consequently, there is strong interest in replacing or reducing the use of fluorochemical compounds such as perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), polytetrafluoroethylene (PTFE), perfluoro-n-decanoic acid (PFDA) and other perfluorinated compounds that are widely used for imparting grease, oil, and/or water resistance to the substrates to which they are applied. [00004] Recently several products have been introduced into the marketplace as potential replacements for the fluorochemical compounds. These materials are based on inorganic materials like silica and on organic polymers, or combinations of those materials. However, to date, these replacements have fallen short of the cost/performance standards established by the fluorinated compounds in this area of use. [00005] It is well known to modify the barrier properties of various materials by the addition of a wax, and paraffin waxes have been used in many of these techniques. Examples of the use of waxes for surface treatment, coating, and the like can be found in U.S. Patent No. 4,117,199. In U.S. Patent No. 4,097,297 to Keene, an oil and water repellant barrier coating is described that consists essentially of a film forming polymer, a fluorochemical surface tension modifier, and a plasticizer. Waxes, coalescing solvents, and dyes are optionally included. [00006] Polyvinyl alcohol) has been widely used in films and coatings for properties that range from water dispersability to barrier properties. Examples of these uses are found in U.S. Patent Nos. 5,468,526, 5,110,390, 5,283,090, 6,113,978, US 2005/0042443 A1 , and GB 2 185 404A, among others. In U.S. Patent No. 5,981 ,011 to Overcash et a/, a coated sheet material is described that has as one component a barrier coating comprising a polymer mixture in which one polymer can be polyvinyl alcohol).
[00007] Several references describe circumstances where either paraffin wax or polyvinyl alcohol) can be used for one purpose or another. For example, in U.S. Patent No. 5,620,793 to Suzuki et al., a printing paper is provided that has no special coating on the printing face and does not cause bronzing in ink-jet printing. The paper also comprises an ink penetration-retarding agent on the printing face that can be, among other things, either polyvinyl alcohol) or paraffin wax. In U.S. Patent No. 5,648,164 to Sakaki et al., a recording paper is described in which both polyvinyl alcohol) or paraffin wax are mentioned as potential ink penetration-retarding agents. In U.S. Patent No. 6,919,111 , to Swoboda et a/., a cellulosic multi-ply paperboard is described that contains predominantly cellulosic fibers, a bulk and porosity enhancing additive, and a size press applied binder coating. The paperboard can be coated with either a binder, such as polyvinyl alcohol), or with a wax. A similar composition having a coating of either a binder such as polyvinyl alcohol) or a wax is described in U.S. Patent No. 6,379,497, to Sandstrom et al. [00008] In U.S. Patent No. 5,843,544 to Andersen et al., hinged starch- bound cellular matrix clam-shell type containers are described that can be coated on the interior with a wax coating. The container can also be coated on the exterior with an elastomeric coating that can comprise polyvinyl alcohol) in order to strengthen the outer surface and reduce its tendency to fracture during the hinging action. Similar articles produced from a starch-bound cellular matrix reinforced with dispersed fibers and having optional coatings of materials such as polyvinyl alcohol) or wax are discussed in U.S. Patent Nos. 5,660,900 and 5,683,772 to Andersen et al. [00009] Wenzel et al., in U.S. Patent Nos. 5,654,039 and 5,837,383, describe recyclable and compostable coated paper stock comprising a substrate having a primer coat that can be polyvinyl alcohol) and, in addition, having a top coat that can include a wax composition, which can be a paraffin wax. However, mixtures of primer coat and top coat materials are not described.
[00010] In U.S. Patent Nos. 5,626,945 to Berzins et al. and 5,635,279 to Ma et al., repulpable, water repellant paperboard is described that has a coating comprising a wax component that can be a paraffin wax, mixed with a polymer matrix of polymer chains ionically cross-linked through pendant carboxylate groups. A preferred polymer matrix was described as comprising a polystyrene-butadiene polymer copolymerized with a monomer having carboxylic acid pendant groups. In the 5,635,279 patent, polyvinyl alcohol) is described as being an ionically cross-linkable polymer that could be used in the invention, however, some carboxylate functionality must be added to the polymer prior to use by copolymerizing with a monomer having carboxylic acid pendant groups. [00011] Other references have described the use of both waxes and substances such as polyvinyl alcohol) for various purposes, in particular in the field of surface preparations for paper and textiles. For example, U.S. Patent No. 5,151,404 to Suzuki et al. describes thermosensitive recording paper that does not curl and provides clear images with high image density. The inventors claim that paraffin wax can be used as a sizing agent in the paper, and polyvinyl alcohol) can be used as a stiffness-imparting agent.
[00012] U.S. Patent No. 5,763,100 to Quick etal., describes recyclable acrylic coated papers that have water and grease resistance and limited moisture vapor transmission characteristics. The papers can have a primer coat, which is commonly a water-based dispersion of a polymer such as polyvinyl alcohol), and a further coating of a water-based emulsion of an acrylic-styrene copolymer and a wax, which can be a paraffin wax.
[00013] In U.S. Patent No. 5,180,614 to Escabasse, a supple biodegradable sheet is described that is resistant to bursting and has poor water and other liquid absorbing power. The sheet comprises fibers, an optional moisture resisting agent, a binder, which can be polyvinyl alcohol), a moisture retaining agent, and a sizing agent, which can be a paraffin wax.
[00014] Dettling, in U.S. Patent No. 5,773,131 , describes a paper product having a flavor seal and a vapor barrier that is produced by applying a primer coating to the paper that can include polyvinyl alcohol), and after polymerizing the coating to form an amorphous net structure, applying a cover coating mixture suitable for generating a vapor seal. The cover coating mixture can include paraffin wax.
[00015] Dragner et ai, in U.S. Patent No. 5,795,932, describe a surface sizing composition for nonwoven substrates that includes a waxy material, that can be a paraffin wax, but is preferably a stearylated melamine, and a surfactantless vinyl polymer or copolymer emulsion that contains an alkali soluble, acid containing copolymer, which acts as the only surfactant for the waxy material. [00016] In U.S. Patent No. 5,928,741 to Andersen et a/., laminated articles fashioned from sheets having a highly inorganically filled organic polymer matrix are described. The sheets can be coated with various materials, selected to improve water penetration, or grease and oil penetration, or to render the article substantially liquid-tight, or pressure- tight, or to increase the flexibility of the article, and polyvinyl alcohol) and waxes are included in a list of several possible coating materials. It is stated that mixtures of the coating materials can also be used, but no particular mixture is identified as being preferred. Methods for the production of articles of a similar nature are described by Andersen et a/, in U.S. Patent Nos. 5,580,409 and 5,800,647.
[00017] In U.S. Patent No. 6,159,612, Chu et al. describe multilayer films having a barrier layer containing a wax. The films are said to provide an effective moisture and oxygen barrier without requiring such barrier agents as polyterpenes, alicyclic hydrocarbons, or high barrier polyvinylidene chloride coatings. The films include a layer comprising an olefin polymer, and a barrier layer comprising a syndiotactic polypropylene homopolymer and a wax. They can further include an outer layer that can be coated, for example, with a polyvinyl alcohol) coating.
[00018] Chang et a/, describe a method of making a flushable film having barrier properties in U.S. Patent No. 6,479,105. The film can have a water-dispersible substrate layer that can comprise polyvinyl alcohol) that is covered with a coating of a low molecular weight amorphous poly(alpha- olefin) that can be admixed with a branched paraffin wax. [00019] In WO 02/14426 to Dixit et a/, (also US 7,019,054) a formulation for providing oil and grease resistance and release paper properties is described as including a fatty acid melamine and paraffin wax emulsion and a polyvinyl alcohol). Alternatively, the formulation can include a fatty acid melamine wax and a polyvinyl alcohol). A preferred fatty acid melamine wax is a stearylated melamine wax. The formulation can be used as a coating to provide oil and grease resistance on paper and paperboard, and can also be applied inline on a paper machine. [00020] Despite the advances that recently have been made in the attempt to find effective and environmentally benign alternatives to fluorochemical barrier coatings, there remains a need for compounds or methods that can be used to reduce the use of or to replace the perfluorinated compounds in present commercial use as greaseproofing and waterproofing agents for paper and the like. It would be useful if such compounds and methods were cost effective and easy to apply. It would also be useful if such compounds and methods were more environmentally benign than the current fluorochemical compounds and it would be useful if such compounds and methods were totally free of such fluorochemical compounds.
SUMMARY OF THE INVENTION
[00021] Briefly, therefore the present invention is directed to a novel method of improving grease and/or water resistance of a material, the method comprising treating the material with wax and polyvinyl alcohol). [00022] The present invention is also directed to a novel composition for improving grease and/or water resistance of a material, the composition comprising wax and polyvinyl alcohol).
[00023] The present invention is also directed to a novel material that has been treated with a composition comprising polyvinyl alcohol) and wax. [00024] The present invention is also directed to a novel material that has been treated with polyvinyl alcohol), wax and a polyamine. [00025] The present invention is also directed to a novel method of improving the gas, water, water vapor, or grease resistance of a porous material, the method comprising: applying to the porous material a first treatment agent; and after the first treatment agent has been applied to the porous material, applying to a surface of the porous material wax, polyvinyl alcohol), and optionally a polyamine, thereby improving the gas, water, water vapor, or grease resistance of the porous material. [00026] The present invention is also directed to a novel porous material having improved gas, water, water vapor and/or grease resistance comprising the porous material having a surface on which is a first coating of a first treatment agent and a second coating comprising wax, polyvinyl alcohol) and optionally a polyamine over the first coating. [00027] The present invention is also directed to a novel porous material that has been treated by the method described above. [00028] Among the several advantages found to be achieved by the present invention, therefore, may be noted the provision of compounds and methods that effectively improve the grease and/or the water resistance of a material and which are cost effective and easy to apply, the provision of such compounds and methods that are more environmentally benign than the current fluorochemical compounds, and the provision of such compounds and methods that require reduced amounts of, or are free of fluorochemical compounds.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS [00029] In accordance with the present invention, it has been discovered that treatment of materials, such as paper, with a combination of wax and polyvinyl alcohol) greatly improves the grease and water resistance of the materials. In preferred embodiments, the degree of improvement is more than would have been expected based merely on the additive effect of the combination. In tests with uncoated paper, coating with wax or polyvinyl alcohol) alone provided grease resistance (reported as Kit numbers measured according to TAPPI TEST METHOD T-559 "Grease Resistance for Paper and Paperboard") of from about 1 - 3, even at dosage rates of up to 0.624 lbs total dry substance per 3000 ft2 of paper (Ib. d.s./3000 ft2). In contrast, however, treatment with a combination of paraffin wax and polyvinyl alcohol) provided protection levels of Kit number 4, even at a dosage as low as 0.156 Ib d.s./3000 ft2, and protection of Kit number 5 at 0.468 lbs d.s./3000 ft2, and Kit number 6 at 0.624 lbs d.s./3000 ft2. [00030] In accordance with the present invention, it has also been discovered that treatment of porous materials, such as paper, with an optional first treatment agent, such as a conventional polymer latex/filler surface coating, followed by a treatment with wax, polyvinyl alcohol) and optionally a polyamine, greatly improves the gas, water, water vapor, and/or grease resistance of the materials, even at relatively low levels of the second treatment. In preferred embodiments, the degree of improvement is more than would have been expected based merely on the additive effect of the two treatments.
[00031] The intent of the invention is that the first treatment step is an optional step, and the first treatment agent is an optional agent. Accordingly, as used herein, reference to the second treatment step, second treatment agent, and/or the second coating will be understood as being the only treatment step or coating when the first treatment step or coating is absent in accordance with the intent of the invention. [00032] In tests with 190# whiteboard, a commercial coating of a polymer latex and filler provided grease resistance (reported as Kit numbers measured according to TAPPI TEST METHOD T-559 "Grease Resistance for Paper and Paperboard") of about zero (0), but treatment of the coated whiteboard with a wax/poly(vinyl alcohol)/polyamine coating, even at dosage rates of under 10 lbs. d.s./ton of paper, improved Kit numbers to about 5, while application of under 15 lbs. d.s./ton improved Kit numbers to about 8, and under 20 lbs. d.s./ton improved Kit numbers to about 12. [00033] Another feature of the present invention is that such superior performance can be obtained without the use of higher, and more expensive, grades of polyvinyl alcohol). It has been shown that the present methods can be carried out successfully with less expensive grades of polyvinyl alcohol), such as partially hydrolyzed and intermediate hydrolyzed polyvinyl alcohol), and that the use of higher grades, such as fully hydrolyzed or super hydrolyzed, is not required. This feature is highly advantageous in controlling the expense of the coating procedure, and improves the cost effectiveness of the innovative method. [00034] In a further embodiment, the inventors have found that the addition of a polyamine to the combination of wax and polyvinyl alcohol) provides additional improvement in the performance of the compositions. For example, a combination of paraffin wax, polyvinyl alcohol), and dicyandiamide-formaldehyde condensate provided protection levels of Kit number 7 at dosage rates of 0.468 lbs d.s./3000 ft2. [00035] When the present specification refers to an improvement in the gas, water, water vapor, and/or grease resistance of a porous material, what is meant is any increase, no matter how small, in the resistance of the porous material to penetration by any type of gas, water, water vapor and/or grease. The term "grease", as used herein, refers to any type of oil, fat, or lipid, whether natural or synthetic, and includes without limitation, natural fats and oils, such as seed oils, including corn oil, soybean oil, rapeseed oil, sunflower oil, and the like, lard, animal fats, and synthetic oils, such as silicone oil and the like, and also liquid, semi-solid and solid hydrocarbons.
[00036] In an embodiment of the invention, improving the gas, water, water vapor, or grease resistance of the porous material comprises increasing the grease resistance of the porous material as measured by Kit number, where the wax, polyvinyl alcohol) and optional polyamine are applied in an amount sufficient to improve the grease resistance by at least 3 Kit numbers. In another embodiment, improving the gas, water, water vapor, or grease resistance of the porous material comprises increasing the grease resistance of the porous material as measured by Kit number, where the wax, polyvinyl alcohol) and optional polyamine are applied in an amount sufficient to improve the grease resistance by at least a factor of 2 but no less than 2 Kit numbers. [00037] In the present specification, the term "coating" is not intended to be limiting to a surface coating, unless that is explicitly stated. By way of example, a coating of the first treatment agent can be applied by adding the first treatment agent to the wet end of a paper machine. The first treatment agent, therefore, is distributed throughout the depth of the paper, but such application is still embraced by the term "coating", as used herein. On the other hand, the terms "surface coating" are meant to refer to a coating that is applied to the outer surface of a porous material, such as a spray or roll coating applied to a dry paper web. [00038] In an embodiment of the present method, the first treatment agent can be any treatment agent that is know for use in sizing, increasing water resistance, gas resistance, water vapor resistance, wet strength, dry strength, softness, drape, hand, and/or the printability of a porous material, except those agents that are not compatible with a subsequent treatment comprising wax and polyvinyl alcohol), optionally with a polyamine. [00039] The first treatment agent can be applied during the formation or manufacture of the porous material, such as at the wet end of a paper machine. Preferably, however, the first treatment agent is applied to a surface of the porous material after the material has been formed. An example of this is the application of the first treatment agent as a coating on paper at the dry end of the paper machine, or at any time after formation of the paper web.
[00040] The first treatment agent can be provided in the form of a waterborne coating formulation or a solventborne coating formulation. Commonly, the first treatment agent comprises a polymer binder. The polymer can be applied neat, as in a hot melt roll application (such as is used for the application of a polyethylene wax to paperboard for the manufacture of milk cartons), or it can be applied as a solution or in a dispersion as a latex. It is common that the polymer is dispersed as a waterborne latex due to the low toxicity, safety and low organic emissions of the application process.
[00041] Examples of polymers that are useful as the polymer binder of the first treatment agent include polyvinyl alcohol), polyacrylate, polystyrene/polyacrylic copolymer, cellulose derivative, nitrocellulose, vinyl chloride, vinyl chloride copolymers, vinyl acrylate copolymers, vinyl acetate homopolymers, vinyl acetate copolymers, styrene butadiene polymers, styrene butadiene acrylonitrile polymers, polyvinylacetate, proteins, milk proteins, starch, and mixtures of any of these.
[00042] In one embodiment, the first treatment agent can include wax, polyvinyl alcohol) and optionally a polyamine. In other words, it can be the same as, or similar to the composition that is used in the subsequent wax/poly(vinyl alcohol) and optional polyamine treatment. [00043] The first treatment agent can have additional components and common additional components can include pigments, such as natural or synthetic pigments; minerals, such as calcium carbonate, titanium dioxide, Kaolin clay, Montmorillionite clay, and gypsum; organic opacifiers; lubricants; surface sizes, such as starch; saturants; release coatings; rheology modifiers; dispersants; insolubilizers; or plasticizers, such as dioctyl phthalate, tricresyl phosphate, and castor oil. The first treatment agent can include any of these materials and any mixtures thereof. In some embodiments, latex binders with inorganic fillers, as described above, are preferred.
[00044] The first treatment agent is applied in any amount that will achieve the beneficial effects described above. However, in some embodiments, it is preferred that the first treatment agent is applied in an amount of from about 0.1 to about 50 g/m2. It is more preferred that the amount of the first treatment agent to be applied is from about 1 to about 30 g/m2, and an amount of from about 2 to about 20 g/m2 is even more preferred.
[00045] Many commercially available materials may be used as the first treatment agent. These include products marketed under the tradenames of RHOPLEX, POLYCO, ROPAQUE, ACUMER and TAMOL, all available from RohmNova, Mogadore, OH. [00046] It should be noted that the present invention embraces the embodiment where the step of applying the first treatment agent is done by another. In other words, the first step of applying the first treatment agent is intended to embrace the act of selecting a pre-coated porous material, to which one can then apply the wax/poly(vinyl alcohol) and optional polyamine.
[00047] Although the present invention offers an advantage of providing superior water and grease resistance with the use of coatings that are free of fluorochemical compounds, the invention also embraces the situation where a reduced amount of a typical fluorochemical water, oil and/or grease proofing agent, such as perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), polytetrafluoroethylene (PTFE), perfluoro-n- decanoic acid (PFDA), or the like, is used in conjunction with the present method to obtain superior Kit numbers. The conventional fluorochemical agent can be applied prior to the present method, or is optionally applied as the first treatment agent, and the second treatment agent is then applied to provide superior levels of grease and/or oil and water resistance. When it is said that a reduced amount of a typical fluorochemical agent is used, it is meant that at least 10% less of the fluorochemical agent is used than would otherwise be required to obtain the Kit number that is achieved when the fluorochemical agent is used in conjunction with the present method. Preferably, the amount of the fluorochemical agent is 25% less, more preferably 50% less than would be required without the use of the novel method.
[00048] In the present method, after the application of the first treatment agent to the porous material (or the selection of a porous material having had a first treatment agent applied to it), wax, polyvinyl alcohol), and optionally a polyamine is applied to a surface of the porous material, thereby improving the gas, water, water vapor, or grease resistance of the porous material. [00049] Any suitable polyvinyl alcohol) can be used in the present methods and compositions. Polyvinyl alcohol) is a polymer comprising vinyl acetate monomer units, some of which have been hydrolyzed to yield alcohol functional groups on the polymer. Polyvinyl acetate) and polyvinyl acetate-co-vinyl alcohol) are also included in the definition of polyvinyl alcohol). The polymer can contain other co-monomers such as ethylene, propylene, butylene, ethylene oxide, propylene oxide, and the like without departing from the scope of the invention. The polyvinyl alcohol) can be in the physical form of a solid, an emulsion, a suspension, or a liquid solution.
[00050] The physical properties of polyvinyl alcohol) are controlled by molecular weight and the degree of hydrolysis, and a wide range of commercial grades is offered by polyvinyl alcohol) manufacturers. Some of the commercially available grades of polyvinyl alcohol) are: Partially Hydrolyzed, Intermediate Hydrolyzed, Fully Hydrolyzed, and Super Hydrolyzed. The molecular weight depends on the conditions of polymerization, and the degree of hydrolysis is defined as the percent of acetate groups replaced by hydroxyl groups during the hydrolysis reaction. The specific gravity of polyvinyl alcohol) solutions depends on concentration and temperature and is independent of grade. Polyvinyl alcohol) reacts in a manner similar to secondary alcohols. [00051] The polyvinyl alcohol) employed in accordance with this invention may be any grade polyvinyl alcohol) that is compatible with paraffin waxes and optionally with polyamines such as dicyandiamide- formaldehyde condensate and that provides improved grease resistance or improved water resistance, or both, when applied to a material, such as paper, in combination with paraffin wax and optionally a polyamine. [00052] In a preferred embodiment, the polyvinyl alcohol) component comprises a partially hydrolyzed polyvinyl alcohol), typically having a percent hydrolysis of about 87% - 89% and a viscosity of about 45 - 55 centipoise (4% aqueous solution at 2O0C). [00053] The manufacture of polyvinyl alcohol) involves starting with polyvinyl acetate and converting that material to polyvinyl alcohol) generally by base-catalyzed methanolysis. Polyvinyl acetate polymerization is done by conventional processes such as, for example, solution, bulk or emulsion polymerization. The polymerization step controls the ultimate molecular weight of the polyvinyl alcohol). Catalyst selection, temperature and solvent control the degree of polymerization. [00054] The degree of hydrolysis of polyvinyl alcohol) is controlled during the alcoholysis reaction and is independent of molecular-weight control. Fully hydrolyzed polyvinyl alcohol) is obtained if methanolysis is allowed to go to completion. The reaction can be terminated by neutralizing or removing the sodium hydroxide catalyst. The addition of small amounts of water to the reactants promotes saponification of polyvinyl acetate, which consumes sodium hydroxide. The extent of hydrolysis is inversely proportional to the amount of water added. Typical degrees of hydrolysis of commercial grades of polyvinyl alcohol) are: Super Hydrolyzed (over 99.3%), Fully Hydrolyzed (98.0 - 98.8%), Intermediate Hydrolyzed (91.0 - 96.5%, with range varying by molecular weight), and Partially Hydrolyzed (86.0 - 89.0, with range varying by molecular weight).
[00055] An example of a commercially-available polyvinyl alcohol) which is partially hydrolyzed and which is suitable for use in the present invention is Celvol 840, which is available from Celanese Corporation of Dallas, TX. [00056] In the present invention, the polyvinyl alcohol) can be used neat, or it can be used in combination with a defoamer. It is not uncommon to add a defoamer when using an intermediate or partially hydrolyzed grade or polyvinyl alcohol).
[00057] Any wax can be used in the methods and compositions of the present invention. Useful waxes may be natural or synthetic, or combinations thereof, and may be macrocrystalline or microcrystalline. The wax can be obtained from animal, vegetable or mineral sources, or it may be produced synthetically. Useful waxes generally have melting points within the range of about 200C to about 2000C, and include animal waxes, mineral waxes, vegetable waxes, insect waxes, and synthetic waxes including: beeswax; bayberry-myrtle; candelilla; caranday; carnauba; castor bean wax; esparto grass wax; Japan wax; montan crude wax; ouricury; retamo-ceri nimbi; shellac wax; spermaceti; sugar cane wax; and wool wax-lanolin.
[00058] Of these waxes, petroleum waxes and synthetic waxes are preferred for the methods and compositions of the present invention. Paraffins and chlorinated paraffin waxes also are of interest as the wax components of the present methods and compositions, as are waxes produced by the emulsion polymerization of ethylene, styrene, or acrylates (weight average molecular weights of about 10,000 to about 50,000). Oxidized hydrocarbon waxes, such as those manufactured from the Fisher-Tropsch paraffins, and the microcrystalline petroleum waxes (ester- type waxes) also are useful in the methods and compositions of the present invention.
[00059] Other synthetic waxes of entirely different structure such as the fatty amides, imides, amines, and nitrites can be waxlike and can be used in the present invention. The polyoxyethylenes or carbowaxes are an important group of waxes because of their solubility properties and compatibility with fatty materials.
[00060] The petroleum waxes, particularly paraffin waxes but also the microcrystalline waxes are particularly preferred for use in the present invention. The petroleum waxes are predominantly long chain (Ci6 -C50) alkane compounds. The paraffins are mostly straight-chain molecules, but may have branched claims. The microcrystalline waxes range in molecular weight from about 400 to about 700 and have average molecules of about 40 to about 50 carbon atoms. The microcrystalline waxes have more branched-chain molecules than in paraffin waxes, containing an average of three carbon atoms per side chain. Oxidized microcrystalline waxes also are useful in the compositions of the present invention. Petroleum waxes contain both solid and liquid hydrocarbons with the liquid hydrocarbons held in discrete droplets within the petroleum wax. The paraffin waxes used in the compositions of the present invention may be crude scale wax and/or fully refined wax.
[00061] Synthetic paraffin waxes are mixtures of saturated straight-chain paraffinic hydrocarbons with short side chains (C1 - C4). The weight average molecular weight is about 700 to about 800 or about 45-60 carbon atoms per molecule.
[00062] Paraffin wax is a preferred wax for use in the present invention. Any type or grade of paraffin wax can be used in the present invention that is compatible with polyvinyl alcohol) and optionally with a polyamine, and that provides improved resistance to grease or improved resistance to water, or both, when applied to a material such as paper in combination with polyvinyl alcohol) and optionally with a polyamine such as dicyandiamide-formaldehyde condensate.
[00063] Preferred paraffin waxes are unbranched or sparsely branched waxy white or colorless solid hydrocarbon mixtures that can be used to make candles, wax paper, lubricants, and sealing materials. The chemical composition of a preferred paraffin wax is a mixture of predominantly non- aromatic saturated hydrocarbons with the general formula CnH(2n+2) where n is preferably an integer between 12 and 50, and more preferably between 22 and 27. It is preferable that the paraffin has a melting point, or melting point range, between about 25°C and about 200° C, more preferably between about 47°C and 95°C, and yet more preferably between about 47°C and abut 65°C, and is insoluble in water. An example of a preferred paraffin wax is available from Sigma-Aldrich, Milwaukee, Wl, as Cat. No. 31 ,765-9, having a CAS RN of 8002-74-2, and a melting point range of 52° - 58°C.
[00064] Other organic materials can be used with, or added to, the wax without departing from the scope of the invention. For example, when the wax is to be used as an aqueous emulsion, it is common to add an emulsifier to the mixture to stabilize the emulsion. A commonly used emulsifier for this purpose is a styrene-acrylate copolymer. Another commonly used material is Morez 101 (a butyl acrylate methyl- methacrylate copolymer available from Rohm & Haas). The wax, water, and the emulsifier can be intermixed with high shear to form a stable emulsion, which can then be used in suitable amounts to produce the compositions of the present invention.
[00065] In some embodiments, it is preferred that paraffin wax and polyvinyl alcohol) be the only materials present that have a significant effect on the grease and/or water resistance of the material. This is advantageous in circumstances where it is desirable to limit the cost or complexity of the treatment. In this instance, the treatment and compositions are said to consist essentially of polyvinyl alcohol) and paraffin wax.
[00066] Optionally, a polyamine can be included as a component of the wax/poly(vinyl alcohol)/polyamine coating. The preferred polyamine is an amine-aldehyde condensate that is the reaction product of an amine containing an active hydrogen atom and an aldehyde. Examples of the amine include guanidine, urea, dicyandiamide, melamine, aniline, ethylenediamine, diethylenetriamine, monoethanolamine, diethanolamine, polyoxyalkyleneamines, polyoxyalkylenediamines, polyoxyalkylenetriamines, and the like. Examples of the aldehyde include formaldehyde, acetaldehyde, glutaraldehyde, glyoxal, hexamethylenetetramine, and paraformaldehyde. Accordingly, examples of polyamines that are useful in the present invention include a condensation product of any one or more of the amines listed above with any one or more of the aldehydes listed above. Polyamines that are useful in the present invention also include, without limitation, polyoxyalkyleneamines, polyoxyalkylenediamines, polyoxyalkylenetriamines, and mixtures of any of these. Examples of these materials include the Jeffamine® series of polyoxyalkyleneamines available from Huntsman Corporation, The Woodlands, TX. [00067] The reaction between the amine and aldehyde is usually conducted in aqueous solution and can be done at acid, neutral, or alkaline pH. The preferred condition is acid pH. Additional information regarding the production of suitable dicyandiamide-formaldehyde condensates can be found, for example, in U.S. Patent 3,957,574 to Anderson.
[00068] A preferred polyamine for the present invention is a dicyandiamide-formaldehyde condensate. Examples of polyamines that are considered to be dicyandiamide-formaldehyde condensates, and which are useful in the invention are available from Polymer Ventures, Inc., Charleston, SC, as RD111-013 and PC-540. RD111-013 is an acid condensation product of dicyandiamide, urea, and formaldehyde, and is available as a clear viscous solution of 46% d.s. having a viscosity of 50 - 250 cps and a pH of about 5.5. It is cationic and has a density of about 10 lbs/gal. PC-540 is an acid condensation product of dicyandiamide, urea, and formaldehyde and is available as a clear viscous solution of 50% d.s. having a viscosity of 10 - 100 cps and a pH of about 3.5. It is cationic and has a density of about 10 lbs/gal. Either of these polyamines can be used as commercially supplied.
[00069] Polyamines, and dicyandiamide-formaldehyde condensates in particular, are described in U.S. Patent No. 6,576,086 by Ettl et al. as being useful as fixing agents in the production of paper or paperboard during paper stock draining. Similar materials are also discussed by Anderson in U.S. Patent' No. 3,957,574 as being preferred dye fixatives in a paper sizing agent. Dicyandiamide-formaldehyde condensates were also discussed as possible replacements for cationic starch in sizing agents in U.S. Patent No. 4,222,820 to Hiskens et al., and as replacements for cationic resins used in a size for ink jet recording paper by Miyamoto in U.S. Patent No. 4,576,867. However, none of these publications suggests the use of these polyamines in combination with a wax and a polyvinyl alcohol) for use to improve grease and/or water resistance as is done in the present invention.
[00070] Furthermore, in U.S. Patent No. 5,423,911 to Coutelle et al. and U.S. Patent No. 5,660,622 to Nikoloff, the use of dicyandiamide- formaldehyde condensates as in paper coatings is described as being undesirable for one reason or another.
[00071] In the present invention, combinations of polyvinyl alcohol) and wax, and optionally, a polyamine, are used in the second coating which provides the superior improvement in gas, water, water vapor and/or grease resistance that has been described.
[00072] When the first treatment agent or the second coating include only polyvinyl alcohol) and wax as the penetration-resistance controlling agents, the two components can be used in any amounts. However, it is preferred that the ratio of the polyvinyl alcohol) to the wax, by weight, is within a range of about 10:90 to about 90:10, a range of about 25:75 to about 75:25 is more preferred, a range of about 40:60 to about 60:40 is even more preferred, and a range of about 45:55 to about 55:45 is yet more preferred. In one embodiment, about 44% polyvinyl alcohol) and about 56% wax, by weight, has been found to provide improved resistance.
[00073] When a polyamine is included in the second coating of the present invention, the polyvinyl alcohol), the wax, and the polyamine can each be included in almost any relative amount. However, it has been found to be preferred that the three components be used in combinations in which the polyvinyl alcohol) is within a range of about 3 to about 74 % by wt. d.s. (where the dry solids (d.s.) include only the three components of interest), the wax is within a range of about 13 - 96 % by wt. d.s., and the polyamine is within a range of about 0.5 - 13 % by wt. d.s. It is more preferred that the three components be used in combinations in which the polyvinyl alcohol) is within a range of about 22 to about 68 % by wt. d.s., the wax is within a range of about 25 - 74 % by wt. d.s., and the polyamine is within a range of about 3 - 12 % by wt. d.s. It is even more preferred that the three components be used in combinations in which the polyvinyl alcohol) is within a range of about 38 to about 68 % by wt. d.s., the wax is within a range of about 25 - 55 % by wt. d.s., and the polyamine is within a range of about 6 - 12 % by wt. d.s. [00074] Alternatively, it has been found that the present methods and compositions can be achieved with combinations of polyvinyl alcohol), wax, and polyamine having a weight ratio of the three components, respectively, of about 4/5/1 , or 5/4/1 , or 4.5/4.5/1.
[00075] In the present invention, the polyvinyl alcohol) and the wax, and optionally the polyamine, can be intermixed into a composition that can be applied to the porous material to be treated. Alternatively, the components can be applied separately. If the components are administered separately, they can be administered at approximately the same time, or they can be administered at different times. By way of example, separate solutions or emulsions of each component can be administered to the material to be treated, or the solutions or emulsions can be intermixed and then applied to the material as a single composition.
[00076] The polyvinyl alcohol), wax, and optionally, the polyamine, of the present invention can be present in the solutions, suspensions, dispersions, or emulsions, or in the compositions of the invention, in almost any concentration. It is preferred that the present compositions contain from about 0.5% to about 60% by weight dry substance, based only on the polyvinyl alcohol), wax, and polyamine, more preferred that they contain from about 1 % to about 50% by wt. d.s., and even more preferred that they contain from about 20% to about 40% by wt. d.s. The present compositions can be diluted prior to use, and after dilution, a d.s. of about 3% to about 10% would be typical, and from about 5% to about 8% d.s. would be preferred. [00077] The wax/poly(vinyl alcohol) and optionally polyamine are applied in a sufficient amount so as to provide the level of performance desired, and that amount may vary widely according to the porous material and its characteristics, such as porosity and surface roughness, as well as the type and amount of the first treatment agent when one is used. The rheological characteristics of the wax/PVOH/optional polyamine coating composition, such as viscosity can also have an affect. When the wax/PVOH/optional polyamine compositions are applied to sheet material having a measurable surface area, such as paper, for example, typical use rates for the present invention, whether only polyvinyl alcohol) and wax are used, or when a polyamine is also included, range from about 0.1 to about 4 lbs dry solids (d.s.) per 3000 ft2 of surface of the material to be treated. It is preferred, however, that the components be applied at a rate of between about 0.1 and about 3 lbs d.s./3000 ft2, even more preferred is an application rate of between about 0.15 to about 2.0 lbs d.s./3000 ft2, more preferred is an application rate of between about 0.15 and 1.0 lbs d.s./3000 ft2, and yet more preferred is an application rate of between about 0.4 and 1.0 lbs d.s./3000 ft2.
[00078] As mentioned above, materials other than the polyvinyl alcohol), wax, and optional polyamine can be used in the second treatment along with these ingredients without departing from the scope of the invention. It has been shown, for example, that it is often desirable to add an emulsifier along with the wax in order to form a stable aqueous emulsion. Other materials, such as colorants, dyes, preservatives, anti-fungal agents, surfactants, and the like, can also be used along with the wax, polyvinyl alcohol) and optional polyamine in the present method. [00079] Although it is possible, and even desirable, to provide and use the wax, the polyvinyl alcohol) and the optional polyamine in aqueous solutions or emulsions, that is not required. In certain circumstances, for example, it might be useful to provide one or more of the components in an organic solvent, or in a molten form, or even in a dry form, such as a powder or flake.
[00080] The methods and compositions of the present invention can be used to treat materials of any sort that would benefit from an improvement in resistance to grease, or resistance to water, or both. The components of the present methods can be applied as coatings or in any other fashion at any point during the manufacture, packaging, storage, or use of the material to be treated.
[00081] When the present methods and compositions are used to form a coating, examples of materials to which they can be applied include packaging and non-packaging materials such as paper, cardboard, bakery board, butter and margarine chips, candy board, cup stock, frozen food containers, plate stock, artist's papers, asphalt laminations, carbonizing tissue, carton overwraps, cover and text papers, envelopes, garbage and trash bags, label papers, paper placemats, release papers, soap containers, wallpaper, liner board, folding cartons, multiwall bags, flexible packaging, duplicator and reproduction papers, support cards and medical dressings.
[00082] In addition, the present methods and compositions can be used to improve grease, oil, and moisture resistance of asphalt, wood, textile fabric, such as woven and non-woven fabrics, yarn, thread, carpets, upholstery, paperboard, formed articles, medical dressings, and the like. [00083] Present materials to be treated are porous, and therefore not impervious to gas, water, water vapor and grease, although such resistance may vary widely. The present porous materials are commonly in sheet form and include substrates comprised of non-woven and woven polymers such as fabrics, and cellulose-based materials, such as paper and cardboard substrates, and the like. As used herein, the terms "sheet material" refer to a material in a form that has length and width dimensions that are each significantly greater than the thickness of the material. Examples of sheet materials include paper, paperboard, housewrap, tarpaper, and the like. The amount of sheet materials can often be characterized in terms of surface area, and the dosage rate of material that is added to a sheet material can be expressed on the basis of the surface area of the material. An example of this type of measurement is a dosage rate expressed as lbs per ft2, or pounds per unit area. [00084] In a preferred embodiment, the paper comprises a porous sheet material made of a cellulosic material, or a cellulose-based material. Such paper sheet materials include, for example, corrugated paperboard (or "cardboard"), newsprint paper, uncorrugated Kraft paper stock, pan liner paper stock, and the like. In addition to paper and paper-like materials, other cellulose-based sheet materials, such as pressed board, may also be suitable. It is also possible to use other fibrous materials for the substrate sheet material.
[00085] As discussed above, the present invention can be used to improve the grease and/or water resistance of paper. When used to treat paper, the first treatment agent alone or along with the first treatment agent and the wax/poly(vinyl alcohol) and optional polyamine can be added to the wet end of a typical Fourdrinier machine, or they can be used to coat paper after it has been dried. Alternatively, the first treatment agent can be added to the wet end of a paper machine and the wax/poly(vinyl alcohol) and optional polyamine can be added as a coating to the paper at the dry end of the machine.
[00086] When the first treatment agent and/or the wax/poly(vinyl alcohol) and optional polyamine are used as a coating, particularly on paper, the components may be applied as a solution, emulsion, or dispersion, by roll coater, brush, doctor blade or blade coater, sprayer or other such suitable application means. Typically, the coated materials are dried after the wax/poly(vinyl alcohol) and optional polyamine has been applied. [00087] After the application of the wax/poly(vinyl alcohol) and optional polyamine, further coatings or treatments may be applied to the material. Such coatings could include heat shielding coatings, UV-resistant coatings, coatings with specific chemical resistance, or the like. [00088] The coated material may be formed into a shaped article by means other than folding and gluing, such as, for example, by pressure- forming. Such shaped articles may be used for cooking or baking purposes. For example, the coated material may be used to make a container for storing food on a shelf (such as for storing pet food) while preventing penetration of grease, oil and/or water through the material. Or the coated material may be used to form a container such as a baking tray. Likewise, the coated material may be used to form a food receptacle such as a paper plate. Or the coated material may be used for fast-food containers, such as boxes for fried chicken, or food wrappers, such as wrapping materials for hamburgers and sandwiches. Thus, the coated material may be used for any of a variety of applications as a food container, wrapper or receptacle.
[00089] The following examples describe preferred embodiments of the invention. Other embodiments within the scope of the claims herein will be apparent to one skilled in the art from consideration of the specification or practice of the invention as disclosed herein. It is intended that the specification, together with the examples, be considered to be exemplary only, with the scope and spirit of the invention being indicated by the claims which follow the examples. In the examples all percentages are given on a weight basis unless otherwise indicated.
EXAMPLE 1.
[00090] This example shows the preparation, application and efficacy of compositions containing wax and polyvinyl alcohol and optionally a polyamine as coatings for paper.
[00091] Paper sheets were supplied from a paper mill in Wisconsin. The sheets were production run non- coated paper having a basis weight of 20 and 20.5 pounds per 3000 square feet. [00092] Sheets were coated with a Gardco automated drawdown machine (available from Paul N. Gardner Company, Inc., Pompano Beach, FL) running at 1.5 cm/ second, using various drawdown rod sizes to give coat weights ranging from 0.05 to 2 dry pounds / 3000 square feet. [00093] Grease resistance tests were conducted in accordance with TAPPI TEST METHOD T-559 "Grease Resistance for Paper and Paperboard"
[00094] Compositions A, B, and C, were made up as aqueous solutions or emulsions with the various components of the present compositions. [00095] Composition A (Polyvinyl alcohol) solution in water). [00096] Distilled water (450 g) was added to a 1 -liter glass reaction flask fitted with a condenser, and temperature probe. Agitation was started using an overhead mixer and a glass rod fitted with a half moon mixing blade. Celvol 840 (50 g), a partially hydrolyzed polyvinyl alcohol) (PVOH) available from Celanese Ltd., was slowly poured into the vortex to ensure full wetting of the PVOH particles. The temperature was then increased to 85-900C and the solution was allowed to cook for 1 hour until the PVOH was fully dissolved.
Composition B (solution of polyfvinyl alcohol) and polyamine in water) [00097] Distilled water (439.5 g) was added to a 1 -liter glass reaction flask fitted with a condenser, and temperature probe. Agitation was started using an overhead mixer and a glass rod fitted with a half moon mixing blade. Then 15.5 g of a 50% active urea-dicyandiamide- formaldehyde copolymer (polyamine) was added. Celvol 840 (45 g) was slowly poured into the vortex to ensure full wetting of the PVOH particles. The temperature was then increased to 85-90°C and the solution was allowed to cook for 1 hour until the PVOH was fully dissolved. Composition C (emulsion of paraffin wax in water with styrene-acrylate copolymer as an emulsion stabilizer)
[00098] Distilled water (300 g), 50 g of Morez 101 (a butyl acrylate methyl-methacrylate copolymer available from Rohm & Haas), and 15Og of paraffin wax (Sigma -Aldrich 52-58°C melting point) was added to a 1 -liter glass reaction flask fitted with a condenser, and temperature probe. Agitation was started using an overhead mixer and a glass rod fitted with a half moon mixing blade. The reactor was heated to 80°C and allowed to mix for 1 hour until both the Morez and paraffin was completely melted. A lab homogenizer (Ultra Turrax T25 from IKA Works, Inc.) was the placed in the reactor and the reactor was allowed to cool to ~ 60°C. At 6O0C the homogenizer was turned on at 24,000 rpm for several minutes. Compositions D - J (mixtures of wax and PVOH and optionally with polvamine)
[00099] Compositions D-J where made in accordance with the relative amounts of components as shown in Table 1. The appropriate amount of Composition A or Composition B was placed in a 500ml beaker fitted with an over head mixing shaft, and the appropriate amount of Example C was slowly added with agitation until the blend was smooth. Table 2 shows the amounts of each of the three ingredients in each of Compositions A - J in terms of the percent by weight of the component relative to the dry weight of the to;tal amounts of wax, polyvinyl alcohol) and urea-dicyandiamide- formaldehyde copolymer condensate in the composition. Accordingly, any amount of other materials, such as emulsifiers, and the like, are not reflected in the calculation shown in Table 2.
Table 1: Grease and water resistance-improving compositions of the present invention having various relative amounts of polyvinyl alcohol) and wax.
Figure imgf000028_0001
Table 2: Relative amounts of components in the compositions of Table 1 in terms of percent dry weight.
Figure imgf000028_0002
Notes: a) PVOH is polyvinyl alcohol) Celvol 840, from Celanese Corporation. b) Wax is paraffin wax having a melting point of 52° - 58°C from Sigma-Aldrich. c) Polyamine is dicyandiamide-formaldehyde condensate. d) (% by wt. d.s.) means the percent of the component relative to the total amount of PVOH, Wax, and Polyamine. e) In the control sample, the paper had no treatment
[000100] All compositions were diluted with distilled water to 2% solids before coating the base sheets. All sheets were coated using a Gardco Automated Draw Down Machine to obtain a specific wet film of coating and then dried on a LabTech Instruments Inc., Speedy Dryer for 3 minutes at 105 °C. Grease resistance was then measured by using TAPPI TEST METHOD T-559 and reported as Kit numbers (Kit #'s). In the last column on the right of Table 3, the 0.1 ml water drop size is an indication of the wetting of the sheet and water repellency. In this test, distilled water (0.1 ml) was applied to the coated sheets using an automatic pipette and the diameter of the water drop on the sheet was measured with a ruler. The larger the water drop diameter, the more wettable the sheet and the lower the water repellency. Those results are shown in Table 3.
Table 3: Kit numbers for grease resistance and water repellency for paper treated with the compositions shown in Tables 1 and 2. Dosage rates were determined by the use of different drawdown rods and the base paper was 20 - 20.5 lb/3000 ft2 basis weight.
Figure imgf000030_0001
Discussion:
[00101] As the data show, compositions A, B, and C alone as a coating at various dosages add little to no grease/oil resistance to the paper substrate. At even the highest levels of application, the highest Kit number obtained was 3. However, upon blending Composition A (PVOH) and Composition C (paraffin wax) a noted increase in Kit number is observed (Kit number 2-3 up to Kit number 5-6), even at the same total dosage of solids. The incorporation of the polyamine into the combination with polyvinyl alcohol) and wax (noted as Composition F), but at the same level of solids dosage, further increases the Kit number to 6-7. [00102] The results for Compositions D-I show that an optimum in grease/ oil resistance is established with the blending of the paraffin wax to the polyvinyl alcohol)/polyamine blend, as indicated by the data in Tables 2 and 3.
[00103] As for water repellency, the uncoated sheet resulted in a water drop diameter of 12 mm compared to a range of 7 - 8 mm for the treated samples. Furthermore, the uncoated sheet resulted in the water spreading over time and soaking into the sheet, whereas the sheets coated with Compositions D - I1 as well as Composition C, showed smaller water drop diameters, thus indicating improved water repellency, and showed no drop spreading over time and no soaking in of the water drop. Paper coated with Compositions A and B showed slightly improved water repellency over the control, however there was some droplet spread over time, but the drops did not soak into the sheets.
[00104] It can be concluded from the data that a combination of wax and polyvinyl alcohol) provided significantly improved grease and water resistance to papers coated with the combination. Because the improvement was obtained without any increase at all in the total amount of solids used for the treatment, It is believed that such an increase is unexpected. Furthermore, when a polyamine was added to the combination, the grease and water resistance was further increased, and again without any increase in the total amount of solids used in the treatment. Therefore, it is believed that the addition of a polyamine to the combination of wax and polyvinyl alcohol) used as a paper coating provides an unexpected improvement in the grease and/or water resistance of the coated material.
EXAMPLE 2.
[00105] This illustrates the efficacy of applying a wax/poly(vinyl alcohol)/polyamine coating to coated and uncoated paperboard according to the present method.
[00106] A coating having the composition of formulation "F" of Example 1 , above, was applied to coated and uncoated 190# whiteboard by using a Gardco Auto Draw Il automated drawdown machine (Paul N. Gardner Company, Inc., Pompano Beach, FL) operating at 1.5 inch/second coat speed and using drawdown wire coating rods of different sizes to obtain coatings of different thicknesses. The coated paperboard had been commercially coated with a polymer latex binder/filler formulation prior to the application of the wax/PVOH/polyamine coating. [00107] The wax/PVOH/polyamine coating comprised 38.4% polyvinyl alcohol) Celvol 840, from Celanese Corporation, 54.9% paraffin wax having a melting point of 52° - 580C from Sigma-Aldrich, and 6.6% dicyandiamide-formaldehyde condensate as the polyamine (all percentages are on a percent of dry matter basis). The components were dispersed in distilled water and applied to the paperboard at a solids concentration of 6% or 8%. Films of several different thicknesses were used. The method of coating and drying was the same as described above in Example 1 , as was the method of measuring grease resistance (Kit Number). Table 4 shows film thicknesses, product application rates and Kit Numbers resulting from coatings placed on uncoated (1 - 8) and coated (9 - 12) paperboard. Table 4: Grease resistance of 190# white paperboard with and without a latex polymer/filler precoat and with different application rates of a wax/PVOH/polyamine second coating.
Figure imgf000033_0001
Notes: a. This refers to the number of pounds of a formulation of the wax/PVOH/polyamine coating at 23% solids in water that was applied per ton of dry paper. That formulation was diluted further prior to application with water to 6% solids for tests 1 - 6 and 9 - 12 and to 8% solids for tests 7 and 8. b. OUN refers to uncoated paperboard with no wax/PVOH/polyamine coating; OCO refers to coated paperboard with no wax/PVOH/polyamine coating.
[00108] The results of this test showed that while the application of a coating comprising wax, PVOH, and polyamine improved the grease resistance of the uncoated whiteboard from 0 Kit number to about 3, as the application rate of the coating formulation increased up to about 170 lbs of the 23% actives formulation/ton of paper (about 39 lbs dry solids/ton of paper), the application of the same coating at a much lower level to pre- coated whiteboard provided unexpectedly superior increases in grease resistance. Coated whiteboard without the subsequent wax/PVOH/polyamine coating had a Kit number of 0. However, the grease resistance of the board increased significantly in a dose-responsive manner up to a Kit number12 at a coating rate of about 19.8 lbs dry solids/ton of paper of the wax/PVOH/polyamine coating (about 85 lbs of the 23% actives formulation/ton of paper).
[00109] Based on the results shown in Example 1 , it is believed that the treatment of a pre-coated porous material with a wax/PVOH coating, without the use of the optional polyamine, would also be useful in increasing the grease resistance of the pre-coated material. [00110] The discussion of the references herein is intended merely to summarize the assertions made by their authors and no admission is made that any reference constitutes prior art. Applicants reserve the right to challenge the accuracy and pertinency of the cited references. [00111] In view of the above, it will be seen that the several advantages of the invention are achieved and other advantageous results obtained. [00112] As various changes could be made in the above methods and compositions by those of ordinary skill in the art without departing from the scope of the invention, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense. In addition it should be understood that aspects of the various embodiments may be interchanged both in whole or in part.

Claims

What is claimed is:
1. A method of improving the gas, water, water vapor, or grease resistance of a material, the method comprising: treating the material with wax, polyvinyl alcohol), and optionally a polyamine, thereby improving the gas, water, water vapor, or grease resistance of the material.
2. The method according to claim 1 , further comprising the step of treating the material with a first treatment agent before the step of treating the material with wax, polyvinyl alcohol), and optionally a polyamine.
3. The method according to claim 2, wherein the step of treating the material with the first treatment agent comprises applying the first treatment agent to a surface of the material to form a first coating.
4. The method according to any of claims 1-3, wherein the step of treating the material with wax, polyvinyl alcohol), and optional polyamine comprises applying the wax, polyvinyl alcohol), and optional polyamine over the first coating to form a wax/poly(vinyl alcohol) coating which optionally comprises a polyamine.
5. The method according to any of claims 1-4, wherein the step of treating the material with wax, polyvinyl alcohol), and optional polyamine comprises applying the wax, polyvinyl alcohol) and polyamine to form a wax/poly(vinyl alcohol)/polyamine coating.
6. The method according to either of claims 1 or 2, wherein improving the gas, water, water vapor, or grease resistance of the material comprises increasing the grease resistance of the material as measured by Kit number and wherein the wax, polyvinyl alcohol) and optional polyamine are applied in an amount sufficient to improve the grease resistance by at least 3 Kit numbers.
7. The method according to either of claims 1 or 2, wherein improving the gas, water, water vapor, or grease resistance of the material comprises increasing the grease resistance of the material as measured by Kit number and wherein the wax, polyvinyl alcohol) and optional polyamine are applied in an amount sufficient to improve the grease resistance by at least a factor of 2 but no less than 2 Kit numbers..
8. The method according to any of claims 1-7, wherein the material comprises a porous material that is selected from the group consisting of paper, asphalt, asphalt laminations, wood, textile fabric, yarn, thread, formed articles and medical dressings.
9. The method according to any of claims 1-7, wherein the material comprises paper and is selected from the group consisting of cardboard, bakery board, butter chips, margarine chips, candy board, cup stock, frozen food containers, plate stock, artist's papers, carbonizing tissue, carton overwraps, cover paper, text paper, envelopes, garbage bags, trash bags, label papers, paper placemats, release papers, soap containers, wallpaper, liner board, folding cartons, multiwall bags, flexible packaging, duplicator paper, reproduction papers, medical dressings, and support cards.
10. The method according to any of claims 1-7, wherein the material comprises textile fabric and is selected from the group consisting of carpet, medical dressings, woven fabrics and non-woven fabrics.
11. The method according to claim 2, wherein the first treatment agent comprises a fluorochemical compound.
12. The method according to claim 2, wherein the first treatment agent comprises a polymer binder.
13. The method according to claim 12, wherein the polymer binder is selected from the group consisting of polyvinyl alcohol), polyacrylate, polystyrene/polyacrylic copolymer, cellulose derivative, nitrocellulose, vinyl chloride, vinyl chloride copolymers, vinyl acrylate copolymers, vinyl acetate homopolymers, vinyl acetate copolymers, styrene butadiene polymers, styrene butadiene acrylonitrile polymers, polyvinylacetate, proteins, milk proteins, starch, and mixtures of any of these.
14. The method according to any of claims 2-10, wherein the first treatment agent comprises wax, polyvinyl alcohol) and optionally a polyamine.
15. The method according to any of claims 2-10, wherein the first treatment agent comprises wax, polyvinyl alcohol) and a polyamine.
16. The method according to any of claims 1-15, wherein the wax is an animal wax, a mineral wax, a vegetable wax, a synthetic wax or a mixture thereof.
17. The method according to claim 16, wherein the wax is selected from the group consisting of paraffin wax, beeswax, bayberry- myrtle, candelilla, caranday, carnauba, castor bean wax, esparto grass wax, Japan wax, montan crude wax, ouricury, retamo-ceri nimbi, shellac wax, spermaceti, sugar cane wax, wool wax-lanolin, polyethylene wax, poly(ethylene-acrylate) wax, or a mixture of any two or more of these.
18. The method according to any of claims 1-17, wherein the polyvinyl alcohol) is selected from the group consisting of super hydrolyzed polyvinyl alcohol), full hydrolyzed polyvinyl alcohol), intermediate hydrolyzed polyvinyl alcohol), partially hydrolyzed polyvinyl alcohol), and mixtures thereof.
19. The method according to claim 18, wherein the polyvinyl alcohol) is intermediate hydrolyzed polyvinyl alcohol) or partially hydrolyzed polyvinyl alcohol).
20. The method according to any of claims 1-18, wherein the step of treating the material comprises applying the polyvinyl alcohol) and the wax to a sheet material at the combined rate of about 0.1 to about 3.0 lbs dry solids (d.s.) per 3000 ft2 of surface of the material.
21. The method according to any of claims 1 -19, wherein the step of treating the material comprises applying the polyvinyl alcohol) and the wax to a sheet material at the combined rate of about 0.15 to about 2.0 lbs d.s./3000 ft2 of surface of the material.
22. The method according to any of claims 1-19, wherein the step of treating the material comprises applying the polyvinyl alcohol) and the wax to a sheet material at the combined rate of about 0.15 to about 1.0 lbs d.s./3000 ft2 of surface of the material.
23. The method according to any of claims 1-22, wherein the treatment comprises applying the polyvinyl alcohol) and the wax to the material in a ratio of the polyvinyl alcohol) to the wax, by weight, that is within a range of about 10:90 to about 90:10.
24. The method according to any of claims 15-24, wherein the polyamine comprises one or more of a polyoxyalkyleneamine, a polyoxyalkylenediamine, a polyoxyalkylenetriamine, or an amine-aldehyde condensate that is the reaction product of an amine containing an active hydrogen atom and an aldehyde.
25. The method according to any of claims 15-24, wherein the polyamine comprises a polyoxyalkyleneamine, a polyoxyalkylenediamine, a polyoxyalkylenetriamine, a dicyandiamide-formaldehyde condensate, or a mixture thereof.
26. The method according to any of claims 15-25, wherein the polyvinyl alcohol), wax, and polyamine are applied in a weight ratio of the three components, respectively, of about 4/5/1 , or 5/4/1 , or 4.5/4.5/1.
27. A porous material that has been treated by the method according to any of claims 1-26.
28. A porous material having improved gas, water, water vapor and/or grease resistance comprising the porous material having a surface on which is a first coating of a first treatment agent and a second coating comprising wax, polyvinyl alcohol) and optionally a polyamine over the first coating.
29. A composition for improving the gas, water, water vapor, or grease resistance of a material, the composition comprising wax, poly (vinyl alcohol), and optionally a polyamine.
30. A composition for improving the gas, water, water vapor, or grease resistance of a material, the composition comprising wax, poly (vinyl alcohol), and a polyamine.
31. The composition according to either of claims 29 or 30, wherein said wax is an animal wax, a mineral wax, a vegetable wax, a synthetic wax, or a mixture thereof.
32. The composition according to any of claims 29-31 , wherein said wax is selected from the group consisting of paraffin wax, beeswax, bayberry-myrtle, candelilla, caranday, camauba, castor bean wax, esparto grass wax, Japan wax, montan crude wax, ouricury, retamo-ceri nimbi, shellac wax, spermaceti, sugar cane wax, wool wax-lanolin, polyethylene wax, poly(ethylene-acrylate) wax, and combinations thereof.
33. The composition according to any of claims 29-32, wherein the polyvinyl alcohol) is selected from the group consisting of super hydrolyzed polyvinyl alcohol), fully hydrolyzed polyvinyl alcohol), intermediate hydrolyzed polyvinyl alcohol), partially hydrolyzed polyvinyl alcohol), and mixtures thereof.
34. The composition according to any of claims 29-33, wherein the polyamine is selected from the group consisting of polyoxyalkyleneamine, polyoxyalkylenediamine, polyoxyalkylenetriamine, an amine-aldehyde condensate that is the reaction product of an amine containing an active hydrogen atom and an aldehyde, and combinations thereof.
35. The composition according to any of claims 30-34, wherein the polyvinyl alcohol), wax, and polyamine are present in the composition in a weight ratio of the three components respectively, of about 4/5/1 , or 5/4/1 , or 4.5/4.5/1.
36. A material having improved gas, water, water vapor and/or grease resistance comprising a material having a composition according to any of claims 29-35 applied as a coating.
PCT/US2006/042149 2005-10-26 2006-10-26 Grease and water resistant article WO2007050964A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CA002624983A CA2624983A1 (en) 2005-10-26 2006-10-26 Grease and water resistant article
EP06826967A EP1940561A4 (en) 2005-10-26 2006-10-26 Grease and water resistant article

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US11/259,491 2005-10-26
US11/259,491 US7282273B2 (en) 2005-10-26 2005-10-26 Grease resistance and water resistance compositions and methods
US11/478,018 US20080003384A1 (en) 2006-06-29 2006-06-29 Multi-layer coatings to increase water and grease resistance of porous materials and materials having such protection
US11/478,018 2006-06-29

Publications (1)

Publication Number Publication Date
WO2007050964A1 true WO2007050964A1 (en) 2007-05-03

Family

ID=37968158

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2006/042149 WO2007050964A1 (en) 2005-10-26 2006-10-26 Grease and water resistant article

Country Status (3)

Country Link
EP (1) EP1940561A4 (en)
CA (1) CA2624983A1 (en)
WO (1) WO2007050964A1 (en)

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8901208B2 (en) 2007-01-25 2014-12-02 Knauf Insulation Sprl Composite wood board
US8900495B2 (en) 2009-08-07 2014-12-02 Knauf Insulation Molasses binder
US8940089B2 (en) 2007-08-03 2015-01-27 Knauf Insulation Sprl Binders
US9040652B2 (en) 2005-07-26 2015-05-26 Knauf Insulation, Llc Binders and materials made therewith
US9309436B2 (en) 2007-04-13 2016-04-12 Knauf Insulation, Inc. Composite maillard-resole binders
WO2016111865A1 (en) * 2015-01-09 2016-07-14 Exxonmobil Research And Engineering Company Wax coating and associated methods of use
US9492943B2 (en) 2012-08-17 2016-11-15 Knauf Insulation Sprl Wood board and process for its production
US9493603B2 (en) 2010-05-07 2016-11-15 Knauf Insulation Sprl Carbohydrate binders and materials made therewith
US9505883B2 (en) 2010-05-07 2016-11-29 Knauf Insulation Sprl Carbohydrate polyamine binders and materials made therewith
US9828287B2 (en) 2007-01-25 2017-11-28 Knauf Insulation, Inc. Binders and materials made therewith
EP3204554A4 (en) * 2014-10-06 2018-03-14 Ecolab USA Inc. Method of increasing paper bulk strength by using a diallylamine acryamide copolymer in a size press formulation containing starch
US10145067B2 (en) 2007-09-12 2018-12-04 Ecolab Usa Inc. Method of improving dewatering efficiency, increasing sheet wet web strength, increasing sheet wet strength and enhancing filler retention in papermaking
US10287462B2 (en) 2012-04-05 2019-05-14 Knauf Insulation, Inc. Binders and associated products
WO2019121733A1 (en) 2017-12-22 2019-06-27 Mitsubishi Hitec Paper Europe Gmbh Recyclable barrier paper
DE102017131276A1 (en) * 2017-12-22 2019-06-27 Mitsubishi Hitec Paper Europe Gmbh Recyclable release substrate
US10508172B2 (en) 2012-12-05 2019-12-17 Knauf Insulation, Inc. Binder
US10767050B2 (en) 2011-05-07 2020-09-08 Knauf Insulation, Inc. Liquid high solids binder composition
US10864653B2 (en) 2015-10-09 2020-12-15 Knauf Insulation Sprl Wood particle boards
US10968629B2 (en) 2007-01-25 2021-04-06 Knauf Insulation, Inc. Mineral fibre board
US11060276B2 (en) 2016-06-09 2021-07-13 Knauf Insulation Sprl Binders
CN113564929A (en) * 2021-07-02 2021-10-29 福可新材料(上海)有限公司 Composition for improving hydrostatic pressure resistance of fluorine-based waterproofing agent and application method thereof
US11242461B2 (en) 2016-10-31 2022-02-08 Sun Chemical Corporation Grease, oil, and water resistant coating compositions
US11248108B2 (en) 2017-01-31 2022-02-15 Knauf Insulation Sprl Binder compositions and uses thereof
US11332577B2 (en) 2014-05-20 2022-05-17 Knauf Insulation Sprl Binders
US11401204B2 (en) 2014-02-07 2022-08-02 Knauf Insulation, Inc. Uncured articles with improved shelf-life
US11549216B2 (en) 2020-11-11 2023-01-10 Sappi North America, Inc. Oil/grease resistant paper products
US11555276B2 (en) 2017-04-28 2023-01-17 Sun Chemical Corporation Heat sealable barrier coating
US11846097B2 (en) 2010-06-07 2023-12-19 Knauf Insulation, Inc. Fiber products having temperature control additives
US11939460B2 (en) 2018-03-27 2024-03-26 Knauf Insulation, Inc. Binder compositions and uses thereof
US11945979B2 (en) 2018-03-27 2024-04-02 Knauf Insulation, Inc. Composite products

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9920485B2 (en) 2015-02-11 2018-03-20 Westrock Mwv, Llc Printable compostable paperboard
US9863094B2 (en) 2015-02-11 2018-01-09 Westrock Mwv, Llc Printable compostable paperboard
US9670621B2 (en) 2015-02-11 2017-06-06 Westrock Mwv, Llc Compostable paperboard with oil, grease, and moisture resistance

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040005341A1 (en) * 2000-08-15 2004-01-08 Dixit Ajit S Formulation for achievement of oil and grease resistance and release paper properties

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2495283A (en) * 1948-05-10 1950-01-24 Du Pont Polymeric polyamine and wax compositions and articles treated therewith
SU1240815A1 (en) * 1985-01-22 1986-06-30 Белорусский Ордена Трудового Красного Знамени Технологический Институт Им.С.М.Кирова Composition for mass sizing of paper and board

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040005341A1 (en) * 2000-08-15 2004-01-08 Dixit Ajit S Formulation for achievement of oil and grease resistance and release paper properties

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1940561A4 *

Cited By (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9260627B2 (en) 2005-07-26 2016-02-16 Knauf Insulation, Inc. Binders and materials made therewith
US9926464B2 (en) 2005-07-26 2018-03-27 Knauf Insulation, Inc. Binders and materials made therewith
US9745489B2 (en) 2005-07-26 2017-08-29 Knauf Insulation, Inc. Binders and materials made therewith
US9464207B2 (en) 2005-07-26 2016-10-11 Knauf Insulation, Inc. Binders and materials made therewith
US9040652B2 (en) 2005-07-26 2015-05-26 Knauf Insulation, Llc Binders and materials made therewith
US9434854B2 (en) 2005-07-26 2016-09-06 Knauf Insulation, Inc. Binders and materials made therewith
US10759695B2 (en) 2007-01-25 2020-09-01 Knauf Insulation, Inc. Binders and materials made therewith
US11905206B2 (en) 2007-01-25 2024-02-20 Knauf Insulation, Inc. Binders and materials made therewith
US11459754B2 (en) 2007-01-25 2022-10-04 Knauf Insulation, Inc. Mineral fibre board
US10968629B2 (en) 2007-01-25 2021-04-06 Knauf Insulation, Inc. Mineral fibre board
US10000639B2 (en) 2007-01-25 2018-06-19 Knauf Insulation Sprl Composite wood board
US9447281B2 (en) 2007-01-25 2016-09-20 Knauf Insulation Sprl Composite wood board
US11401209B2 (en) 2007-01-25 2022-08-02 Knauf Insulation, Inc. Binders and materials made therewith
US9828287B2 (en) 2007-01-25 2017-11-28 Knauf Insulation, Inc. Binders and materials made therewith
US11453780B2 (en) 2007-01-25 2022-09-27 Knauf Insulation, Inc. Composite wood board
US8901208B2 (en) 2007-01-25 2014-12-02 Knauf Insulation Sprl Composite wood board
US9309436B2 (en) 2007-04-13 2016-04-12 Knauf Insulation, Inc. Composite maillard-resole binders
US8940089B2 (en) 2007-08-03 2015-01-27 Knauf Insulation Sprl Binders
US9469747B2 (en) 2007-08-03 2016-10-18 Knauf Insulation Sprl Mineral wool insulation
US8979994B2 (en) 2007-08-03 2015-03-17 Knauf Insulation Sprl Binders
US9039827B2 (en) 2007-08-03 2015-05-26 Knauf Insulation, Llc Binders
US11946582B2 (en) 2007-08-03 2024-04-02 Knauf Insulation, Inc. Binders
US10145067B2 (en) 2007-09-12 2018-12-04 Ecolab Usa Inc. Method of improving dewatering efficiency, increasing sheet wet web strength, increasing sheet wet strength and enhancing filler retention in papermaking
US9416248B2 (en) 2009-08-07 2016-08-16 Knauf Insulation, Inc. Molasses binder
US10053558B2 (en) 2009-08-07 2018-08-21 Knauf Insulation, Inc. Molasses binder
US8900495B2 (en) 2009-08-07 2014-12-02 Knauf Insulation Molasses binder
US9505883B2 (en) 2010-05-07 2016-11-29 Knauf Insulation Sprl Carbohydrate polyamine binders and materials made therewith
US11814481B2 (en) 2010-05-07 2023-11-14 Knauf Insulation, Inc. Carbohydrate polyamine binders and materials made therewith
US10738160B2 (en) 2010-05-07 2020-08-11 Knauf Insulation Sprl Carbohydrate polyamine binders and materials made therewith
US9493603B2 (en) 2010-05-07 2016-11-15 Knauf Insulation Sprl Carbohydrate binders and materials made therewith
US10913760B2 (en) 2010-05-07 2021-02-09 Knauf Insulation, Inc. Carbohydrate binders and materials made therewith
US11078332B2 (en) 2010-05-07 2021-08-03 Knauf Insulation, Inc. Carbohydrate polyamine binders and materials made therewith
US11846097B2 (en) 2010-06-07 2023-12-19 Knauf Insulation, Inc. Fiber products having temperature control additives
US10767050B2 (en) 2011-05-07 2020-09-08 Knauf Insulation, Inc. Liquid high solids binder composition
US11725124B2 (en) 2012-04-05 2023-08-15 Knauf Insulation, Inc. Binders and associated products
US10287462B2 (en) 2012-04-05 2019-05-14 Knauf Insulation, Inc. Binders and associated products
US11453807B2 (en) 2012-04-05 2022-09-27 Knauf Insulation, Inc. Binders and associated products
US9492943B2 (en) 2012-08-17 2016-11-15 Knauf Insulation Sprl Wood board and process for its production
US10183416B2 (en) 2012-08-17 2019-01-22 Knauf Insulation, Inc. Wood board and process for its production
US10508172B2 (en) 2012-12-05 2019-12-17 Knauf Insulation, Inc. Binder
US11384203B2 (en) 2012-12-05 2022-07-12 Knauf Insulation, Inc. Binder
US11401204B2 (en) 2014-02-07 2022-08-02 Knauf Insulation, Inc. Uncured articles with improved shelf-life
US11332577B2 (en) 2014-05-20 2022-05-17 Knauf Insulation Sprl Binders
EP3204554A4 (en) * 2014-10-06 2018-03-14 Ecolab USA Inc. Method of increasing paper bulk strength by using a diallylamine acryamide copolymer in a size press formulation containing starch
US10030171B2 (en) 2015-01-09 2018-07-24 Exxonmobil Research And Engineering Company Wax coating and associated methods of use
WO2016111865A1 (en) * 2015-01-09 2016-07-14 Exxonmobil Research And Engineering Company Wax coating and associated methods of use
US10864653B2 (en) 2015-10-09 2020-12-15 Knauf Insulation Sprl Wood particle boards
US11230031B2 (en) 2015-10-09 2022-01-25 Knauf Insulation Sprl Wood particle boards
US11060276B2 (en) 2016-06-09 2021-07-13 Knauf Insulation Sprl Binders
US11242461B2 (en) 2016-10-31 2022-02-08 Sun Chemical Corporation Grease, oil, and water resistant coating compositions
US11248108B2 (en) 2017-01-31 2022-02-15 Knauf Insulation Sprl Binder compositions and uses thereof
US11555276B2 (en) 2017-04-28 2023-01-17 Sun Chemical Corporation Heat sealable barrier coating
WO2019121733A1 (en) 2017-12-22 2019-06-27 Mitsubishi Hitec Paper Europe Gmbh Recyclable barrier paper
DE102017131276A1 (en) * 2017-12-22 2019-06-27 Mitsubishi Hitec Paper Europe Gmbh Recyclable release substrate
DE102017131277A1 (en) * 2017-12-22 2019-06-27 Mitsubishi Hitec Paper Europe Gmbh Recyclable barrier paper
EP3508545B1 (en) 2017-12-22 2021-05-05 Mitsubishi HiTec Paper Europe GmbH Recyclable release substrate
US11939460B2 (en) 2018-03-27 2024-03-26 Knauf Insulation, Inc. Binder compositions and uses thereof
US11945979B2 (en) 2018-03-27 2024-04-02 Knauf Insulation, Inc. Composite products
US11549216B2 (en) 2020-11-11 2023-01-10 Sappi North America, Inc. Oil/grease resistant paper products
CN113564929A (en) * 2021-07-02 2021-10-29 福可新材料(上海)有限公司 Composition for improving hydrostatic pressure resistance of fluorine-based waterproofing agent and application method thereof

Also Published As

Publication number Publication date
EP1940561A1 (en) 2008-07-09
EP1940561A4 (en) 2009-09-23
CA2624983A1 (en) 2007-05-03

Similar Documents

Publication Publication Date Title
US20080003384A1 (en) Multi-layer coatings to increase water and grease resistance of porous materials and materials having such protection
WO2007050964A1 (en) Grease and water resistant article
US7282273B2 (en) Grease resistance and water resistance compositions and methods
US20090098303A1 (en) Coatings to increase water and grease resistance of porous materials and materials having such protection
KR101802620B1 (en) Process for producing a coated packaging material and packaging material having at least one barrier layer for hydrophobic compounds
US7019054B2 (en) Formulation for achievement of oil and grease resistance and release paper properties
AU726025B2 (en) Sizing composition
US20070232743A1 (en) Method of forming a vapor impermeable, repulpable coating for a cellulosic substrate and a coating composition for the same
WO2010141581A1 (en) Cationic wet strength resin modified pigments in water-based latex coating applications
KR20120053514A (en) Novel treated mineral pigments for aqueous based barrier coatings
WO2014192931A1 (en) Composite paper having oil resistance
CN113382834A (en) Novel aqueous binder using sugar fatty acid ester
CN1330699C (en) Vapor screen composition
WO2019189229A1 (en) Paper barrier material
JP4371906B2 (en) Undercoat coating liquid for water repellent layer, water repellent paper having the coating layer, and method for producing the same
JP2019173259A (en) Paper-made barrier material
US3792128A (en) Fluoropolymer-carboxylated styrene-butadiene functional surface coating compositions
JP3763173B2 (en) Moisture-proof laminate
JP3028468B2 (en) Paper strength enhancer composition and paper sizing composition
CA3197366A1 (en) Enhanced cellulose nanofibrils (cnf)
JP2023088053A (en) Coating agent for paper substrate
WO2024081557A1 (en) Processes for imparting oil and grease resistance to paper products

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)
ENP Entry into the national phase

Ref document number: 2624983

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2006826967

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: MX/a/2008/005446

Country of ref document: MX

NENP Non-entry into the national phase

Ref country code: DE