WO2014179946A1 - Water and oil-repellent fluoropolymer having a short perfluorinated chain - Google Patents

Water and oil-repellent fluoropolymer having a short perfluorinated chain Download PDF

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WO2014179946A1
WO2014179946A1 PCT/CN2013/075321 CN2013075321W WO2014179946A1 WO 2014179946 A1 WO2014179946 A1 WO 2014179946A1 CN 2013075321 W CN2013075321 W CN 2013075321W WO 2014179946 A1 WO2014179946 A1 WO 2014179946A1
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Prior art keywords
water
hfo
group
oil repellent
nanoparticles
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PCT/CN2013/075321
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French (fr)
Inventor
Shijun FENG
Andrew J. Poss
Rajiv R. Singh
Yun Lin
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Honeywell International Inc.
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Priority to JP2016512184A priority Critical patent/JP2016526113A/en
Priority to US14/889,047 priority patent/US20160083605A1/en
Priority to PCT/CN2013/075321 priority patent/WO2014179946A1/en
Priority to CN201380076312.4A priority patent/CN105492549A/en
Priority to EP13883883.4A priority patent/EP2994510A4/en
Publication of WO2014179946A1 publication Critical patent/WO2014179946A1/en

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    • 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
    • C09D127/00Coating 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 a halogen; Coating compositions based on derivatives of such polymers
    • C09D127/02Coating 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
    • C09D127/12Coating 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 a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
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    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/16Antifouling paints; Underwater paints
    • C09D5/1656Antifouling paints; Underwater paints characterised by the film-forming substance
    • C09D5/1662Synthetic film-forming substance
    • C09D5/1668Vinyl-type polymers
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    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/77Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
    • D06M11/79Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof with silicon dioxide, silicic acids or their salts
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    • 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
    • D06M15/244Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
    • D06M15/248Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing chlorine
    • DTEXTILES; PAPER
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    • 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
    • D06M15/244Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
    • D06M15/256Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing fluorine
    • DTEXTILES; PAPER
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    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M23/00Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
    • D06M23/08Processes in which the treating agent is applied in powder or granular form
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2227Oxides; Hydroxides of metals of aluminium
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
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    • C08K2003/2237Oxides; Hydroxides of metals of titanium
    • C08K2003/2241Titanium dioxide
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
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    • C08K2003/2296Oxides; Hydroxides of metals of zinc
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    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
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    • C08K3/22Oxides; Hydroxides of metals
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
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    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
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    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/18Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/20Polyalkenes, polymers or copolymers of compounds with alkenyl groups bonded to aromatic groups
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    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/18Synthetic fibres consisting of macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M2101/24Polymers or copolymers of alkenylalcohols or esters thereof; Polymers or copolymers of alkenylethers, acetals or ketones
    • DTEXTILES; PAPER
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    • D06M2101/16Synthetic fibres, other than mineral fibres
    • D06M2101/30Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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    • D06M2200/00Functionality of the treatment composition and/or properties imparted to the textile material
    • D06M2200/10Repellency against liquids
    • D06M2200/11Oleophobic properties
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    • D06M2200/10Repellency against liquids
    • D06M2200/12Hydrophobic properties

Definitions

  • the present invention relates to fluorinated polymers having water and oil-repellent properties. More specifically, the present invention relates to the coating of textile fabrics with such fluorinated polymers.
  • polyfluoroalkyl group having at least 8 carbon atoms See, for example, U.S. Pat. No. 5,334,903 (Raiford et al), U.S. Pat. No. 4,321,404 (Williams et al), U.S.Pat. No. 5,144,056 (Anton et al.) and U.S. Pat. No. 5,446,118 (Shen et al.).
  • Takao et al. U.S. Patent Application Publication No. 2012/02590405 discloses the use of perfluoroalkyethyl acrylate/vinylidene chloride/ alkyl(meth)acrylate copolymer emulsions, which, after application to nylon and polyester cloths from an emuslion formulation, imparted oil and water repellency to the substrates.
  • the chemical formula for a perfluoroalkyl ethyl acrylate monomer is used by Takao et al. is as follows:
  • Gregg et al. (U.S. Patent Application Publication No. 2007/0173149) disclose another kind of fluoroacrylate having an R group having less than 6 carbon atoms, which is even shorter than the monomer used by Takeo et al.
  • the chemical structure of one monomer used by Gregg et al. is as follows:
  • the present invention addresses this need by providing fiuoropolymers having fewer than 4 R groups which can be used for water and oil repellency coatings, and can serve in coating solutions on articles such as woven and nonwoven textile fabrics made from natural and/or synthetic fibers, including, but not limited to, cotton, cellulose, wool, silk, polyamide, polyester, polyolefm, polyacrylonitrile, paper, and leather.
  • a water and oil repellent coating for textile fabrics is provided, the coating having a low energy portion containing the polyolefm, and a nanometer portion containing nanoparticles which change the morphology of the textile fabric.
  • the polyolefm comprises at least one fluoropolymer represented by the following formula: wherein R ls R 2 , R3 are each selected from H, CI and F, m is an integer, and the polymer has a molecular weight between 1000 and 100,000.
  • this polymer can be synthesized in presence of initiator in a reaction solution.
  • a textile fabric having the coating in accordance with the first aspect is provided.
  • a method of a coating the textile fabric with the coating of the first aspect is provided.
  • FIG.l is a flow chart of a method of producing an water and oil repellent coating on fabrics.
  • FIG. 1 is a flow chart illustrating a method of forming an hydrophobic and olephobic coating on fabrics.
  • the resulting polymer is represented by the following formula: wherein R ls R 2 , R 3 are each selected from H, CI and F, and the polymer has a molecular weight between 1000 and 100,000.
  • HFOs hydrofluoroolefms
  • Suitable HFOs include tetrafluoropropene compounds and pentafluoropropene compounds.
  • a preferred tetrafluoropropene compound is 2,3,3,3-tetrafluoro-l-propene (HFO-1234yf), which forms a polymer having the following formula: [0016]
  • Other suitable tetrafluoropropene compounds include HFO-1234ze, HFO-1233zd, and HFO-1234zf.
  • Suitable pentafluoropropene compounds include HFO-1225. Stereoisomers of any the foregoing compounds may also be suitable.
  • Polymerization is preferably carried out in the presence of one or more free-radical initiators.
  • Suitable initiators include azodiisobutyronitrile, 2,2'-azobis(2- methylpropionamide)dihydrochloride, aliphatic perester such as tertbutylhydroperoxide, persulfates such as sodium persulfate, potassium persulfate, ammonium persulfate, and iron persulfate, and combinations of the foregoing.
  • a persulfate initiator may be particularly suitable for the present invention.
  • the initiator may be less than 10 wt%, more particularly less than 5 wt % and even more particularly less than 1.0 wt% based on the total weight of monomer.
  • a preferred method for synthesizing a 1234yf homo-polymer in accordance with the present invention is emulsion polymerization.
  • One benefit of this method is that no
  • chlorofluorocarbon or common solvents are used.
  • the process is enviromentally benign.
  • Other common alternative methods, such as solution polymerization and bulk polymerization may also be used.
  • Surfactants which may used during the preparation of 1234yf homo-polymer include, but are not limited to, fluorosurfactants and hydrocarbon surfactants (such as sodium octyl sulfonate, sodium dodecylsulfonates, sodium decyl sulfate, sodium caprylate, sodium stearate, and nonylphenolpoly(ethylene oxide)).
  • fluorosurfactant or perfluorinated carboxylic acid is employed, such as the ammonium perfluorooctonoate in the specific examples.
  • the 1234yf homopolymer produced in accordance with the present invention was identified by NMR method and elemental analysis.
  • the 1234yf homopolymer has good solubility in some common organic solvents, such as ethyl acetate and methyl ethyl ketone. Accordingly, fluoropolymers can be used to coat fabrics in solution form. Preferably the coating solutions are between 0.5 and 95 wt% fluoropolymer, and even more preferably, between 0.5 and 5.0 wt% fluoropolymer.
  • Preferred nanoparticles for the present invention include silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide and combinations of the foregoing.
  • Example 2 below provides a typical procedure for producing nanoparticles.
  • This nanoparticle dispensed solution i.e., component B
  • Preferred textile fabrics include, but are not limited to, a variety of woven and nonwoven textile fabrics made from natural or synthetic fibers including cotton, cellulose , wool, silk, polyamide, polyester, polyolefm, polyacrylonitrile, and rayon.
  • An amount of the Homo-1234yf solid was diluted with butanone to a polymer content of 0.5-5% as component A, silicon dioxide nanopaticle solution prepared above is used as component B.
  • the fabrics selected for testing included a blue nylon , PET, a polyolefm nonwoven, and undyed cotton fabrics. Prior to testing, the polyolefm fabric was dried at room temperature for 24 hours and then heat-treated at 38°C for 10 seconds. The nylon fabric was air dried for 24 hours before use. The fabrics were immersed into component B system first for 3 minutes, followed by curing at 80 °C for 3 minutes, and 150 °C for 3 minutes respectively.
  • the silicon dioxide nanoparticle solution was diluted to 0.05 mass % with distilled water which had been passed through a 50 ⁇ filter to obtain a sample.
  • the average particle size of the sample was measured by dynamic light scattering method via a particle size measurement, system. The average particle size was found to be 180nm.
  • the water repellency was evaluated in accordance with the spray test method (AATCC standard test method No. 22). During the test, 250 ml of water was poured in a narrow stream at a 27 degree angle onto a fabric sample stretched on a 6-inch (15.2 cm) diameter plastic hoop, discharged from a funnel suspended 6 inches above the fabric sample. After removal of excess water, the fabric was visually scored by reference to published standards. A rating of 100 denotes no water penetration or surface adhesion; a rating of 90 denotes slight random sticking or wetting, and lower values indicate greater wetting. A rating of 0 indicates complete wetting. Testing results for water repellency rating were 95 for PET, 95 for nylon and 90 for cotton fabric respectively, indicating very good water repellency which results in the beading of water on the fabrics.
  • the treated fabric samples were tested for oil repellency by a modification of AATCC standard test method No. 118.
  • a series of organic liquids, identified below in Table 2 were introduced dropwise to the fabric samples. Beginning with the lowest numbered test liquid (Repellency rating No. 1), one drop (0.05mL volume) was placed on each of three locations at least 5 mm apart. The drops were observed for 30 seconds. If, at the end of this period, two of the three drops were still spherical to hemispherical in shape with no wicking around the drops, three drops of the next highest numbered liquid were placed on adjacent sites and similarly observed for 30 seconds.
  • the procedure was continued until one of the test liquids results in two of the three drops failing to remain spherical to hemispherical, or wetting or wicking occurs.
  • the oil-repellency rating of the fabric is the highest numbered test liquid for which two of the three drops remain spherical to hemispherical, with no wicking for 30 seconds.
  • oil repellency rating was found to be 4 for PET, 4 for Nylon and 3 for cotton fabrics, indicating that the fabrics have good oil repellency rating.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Paints Or Removers (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Abstract

Disclosed water and oil repellent coatings for textile fabrics having a low surface energy portion having a polyolefin having a Rf of 4 or less, and a nanometer portion which has nanoparticles. Also disclosed coated fabrics, as well as methods for making the coated fabrics.

Description

WATER AND OIL-REPELLENT FLUOROPOLYMER HAVING A SHORT
PERFLUORINATED CHAIN
FIELD OF THE INVENTION
[0001] The present invention relates to fluorinated polymers having water and oil-repellent properties. More specifically, the present invention relates to the coating of textile fabrics with such fluorinated polymers.
BACKGROUND OF THE INVENTION
[0002] For many years, a popular and typical method for imparting water/oil repellency to a surface of an article (e.g., fiber products, PET synthesized fibers) was to immerse substrates into a coplymer emulsion having structural units based on a monomer having a
polyfluoroalkyl group having at least 8 carbon atoms. See, for example, U.S. Pat. No. 5,334,903 (Raiford et al), U.S. Pat. No. 4,321,404 (Williams et al), U.S.Pat. No. 5,144,056 (Anton et al.) and U.S. Pat. No. 5,446,118 (Shen et al.).
[0003] However, as discussed in, inter alia, U.S. Pat. No. 5,688,884 (Baker et al), the United States Enviromental Protection Agency (EPA) has made findings that a compound having a perfiuoroalkyl group (R group) with at least 8 carbon atoms is slow to decompose, is likely to be bio-accumulated in living organisms, and potentially presents a high impact on the environment. Accordingly, studies have been made to determine whether a polymer or copolymer which has structural units based on a monomer having a R group having less than 8 carbon atoms would be effective as a water/ oil repellent composition.
[0004] For example, Takao et al. (U.S. Patent Application Publication No. 2012/0259045) discloses the use of perfluoroalkyethyl acrylate/vinylidene chloride/ alkyl(meth)acrylate copolymer emulsions, which, after application to nylon and polyester cloths from an emuslion formulation, imparted oil and water repellency to the substrates. The chemical formula for a perfluoroalkyl ethyl acrylate monomer is used by Takao et al. is as follows:
CF3(CF2)5-C2H4-OC(0)CH=CH2
[0005] Gregg et al. (U.S. Patent Application Publication No. 2007/0173149) disclose another kind of fluoroacrylate having an R group having less than 6 carbon atoms, which is even shorter than the monomer used by Takeo et al. For example, the chemical structure of one monomer used by Gregg et al. is as follows:
CF3(CF2)3S02N(CH3)(CH2)m-OC(0)NH-(C6H4-CH2-C6H4)-HNC(0)0-(CH2)n(0)COC=CH2 (m= 2 to 8, n=2 to 30)
[0006] As likewise indicated in Gregg et al, it was expected that having fewer R groups made the compounds less toxic and less bioaccumulative than 6 carbon or 8 carbon perfluorinated groups, while maintaining good water/ oil repellency ability.
[0007] Accordingly, there is a need to develop fluoropolymer which is even more enviromentally conscious, e.g., having fewer than R groups and having relatively good hydrophobic and oleophobic properties.
SUMMARY OF THE INVENTION
[0008] The present invention addresses this need by providing fiuoropolymers having fewer than 4 R groups which can be used for water and oil repellency coatings, and can serve in coating solutions on articles such as woven and nonwoven textile fabrics made from natural and/or synthetic fibers, including, but not limited to, cotton, cellulose, wool, silk, polyamide, polyester, polyolefm, polyacrylonitrile, paper, and leather. [0009] In accordance with a first aspect of the present invention, a water and oil repellent coating for textile fabrics is provided, the coating having a low energy portion containing the polyolefm, and a nanometer portion containing nanoparticles which change the morphology of the textile fabric. Preferably, the polyolefm comprises at least one fluoropolymer represented by the following formula:
Figure imgf000005_0001
wherein Rls R2, R3 are each selected from H, CI and F, m is an integer, and the polymer has a molecular weight between 1000 and 100,000. Preferably, this polymer can be synthesized in presence of initiator in a reaction solution.
[0010] In accordance with a second aspect of the present invention, a textile fabric having the coating in accordance with the first aspect is provided.
[0011] In accordance with a third aspect of the present invention, a method of a coating the textile fabric with the coating of the first aspect is provided.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012] A specific example has been chosen for purposes of illustration and description, and is shown in the accompanying drawing, forming a part of the specification.
[0013] FIG.l is a flow chart of a method of producing an water and oil repellent coating on fabrics. DETAILED DESCRIPTION
[0014] FIG. 1 is a flow chart illustrating a method of forming an hydrophobic and olephobic coating on fabrics. According to the method, water/ oil repellent coating is formed by polymerizing a fluorocarbon compound of the general formula CF3CRi=CR2R3 in the presence of an initiator and under suitable reaction conditions. The resulting polymer is represented by the following formula:
Figure imgf000006_0001
wherein Rls R2, R3 are each selected from H, CI and F, and the polymer has a molecular weight between 1000 and 100,000.
[0015] After forming the polymer, acid may be added to precipitate the polymer. The precipitated polymer may then be filtered, dried and combined with common organic solvent to form a key component (i.e., component A). A variety of commercially available hydrofluoroolefms or (HFOs) may be used to prepare the fluoropolymer. Suitable HFOs may have the general formula CF3CRi=CR2R3, wherein Rls R2, R3 are each selected from H, CI and F. Suitable HFOs include tetrafluoropropene compounds and pentafluoropropene compounds. A preferred tetrafluoropropene compound is 2,3,3,3-tetrafluoro-l-propene (HFO-1234yf), which forms a polymer having the following formula:
Figure imgf000006_0002
[0016] Other suitable tetrafluoropropene compounds include HFO-1234ze, HFO-1233zd, and HFO-1234zf. Suitable pentafluoropropene compounds include HFO-1225. Stereoisomers of any the foregoing compounds may also be suitable.
[0017] Polymerization is preferably carried out in the presence of one or more free-radical initiators. Suitable initiators include azodiisobutyronitrile, 2,2'-azobis(2- methylpropionamide)dihydrochloride, aliphatic perester such as tertbutylhydroperoxide, persulfates such as sodium persulfate, potassium persulfate, ammonium persulfate, and iron persulfate, and combinations of the foregoing. A persulfate initiator may be particularly suitable for the present invention. The initiator may be less than 10 wt%, more particularly less than 5 wt % and even more particularly less than 1.0 wt% based on the total weight of monomer.
[0018] A preferred method for synthesizing a 1234yf homo-polymer in accordance with the present invention is emulsion polymerization. One benefit of this method is that no
chlorofluorocarbon or common solvents are used. The process is enviromentally benign. Other common alternative methods, such as solution polymerization and bulk polymerization may also be used.
[0019] Surfactants which may used during the preparation of 1234yf homo-polymer include, but are not limited to, fluorosurfactants and hydrocarbon surfactants (such as sodium octyl sulfonate, sodium dodecylsulfonates, sodium decyl sulfate, sodium caprylate, sodium stearate, and nonylphenolpoly(ethylene oxide)). Preferably, fluorosurfactant or perfluorinated carboxylic acid is employed, such as the ammonium perfluorooctonoate in the specific examples. [0020] The 1234yf homopolymer produced in accordance with the present invention was identified by NMR method and elemental analysis. As shown in Table 1 below, the 1234yf homopolymer has good solubility in some common organic solvents, such as ethyl acetate and methyl ethyl ketone. Accordingly, fluoropolymers can be used to coat fabrics in solution form. Preferably the coating solutions are between 0.5 and 95 wt% fluoropolymer, and even more preferably, between 0.5 and 5.0 wt% fluoropolymer.
Table 1 : Homo-1234yf solubility test results
Figure imgf000008_0001
[0021] Preferred nanoparticles for the present invention include silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide and combinations of the foregoing. Example 2 below provides a typical procedure for producing nanoparticles. This nanoparticle dispensed solution (i.e., component B) is preferably used to form the bottom layer on the textile fabrics before making an upper, low-surface energy fluoropolymer layer coating.
[0022] Preferred textile fabrics include, but are not limited to, a variety of woven and nonwoven textile fabrics made from natural or synthetic fibers including cotton, cellulose , wool, silk, polyamide, polyester, polyolefm, polyacrylonitrile, and rayon.
EXAMPLES
Example 1
Polymerization of 2,3,3,3-tetrafluoro-l-propene polymer (Homo-1234yf)
[0023] To a 1000 mL autoclave was added 450 mL deionized water, 6 g ammonium perfluorooctonoate, 1.2 g ammonium persulfate, 3.36 g Na2HP04 and 2.22 g NaH2P04.2H20. After 3 cycles of deoxygenation with nitrogen, the mixture solution was cooled to 0°C, 360 g 2,3,3,3-tetrafluoropropene monomer was charged into the high pressure reactor via a pump over a period of 5 minutes, during which the reactor contents were stirred at 200 rpm. After the monomer feeding step, the reactor was held at 400rpm and 70°C. After 48 hours, the polymerization was stopped and excessive gas was released from the autoclave. The polymerization latex was coagulated in 25% HC1 and the polymerization product was washed with distilled water and dried 50 °C overnight. Finally, 237.15 g white polymer was obtained with a yield of 66%. The product was an amorphous fluoroelastomer having a glass transition temperature of 54 °C as determined by differential scanning calorimetry (DSC). Fluorine content was found to be 66.5%>. Example 2
Preparation of silicon dioxide nanoparticle solution
[0024] To a 250 mL round bottom flask with a magnetic stirrer was added 10 mL deionized water, 25 mL ethanol and 35 mL tetraethyl orthosilicate. After 10 minutes reaction at room temperature at a stirring speed of 400rpm, a few drops of base and/or acid was added to the reaction solution slowly. After 2 hours, the silicon dioxide nanoparticle solution is formed and can be used directly.
Example 3
Preparation of water and oil repellent coating on fabric
[0025] An amount of the Homo-1234yf solid was diluted with butanone to a polymer content of 0.5-5% as component A, silicon dioxide nanopaticle solution prepared above is used as component B. The fabrics selected for testing included a blue nylon , PET, a polyolefm nonwoven, and undyed cotton fabrics. Prior to testing, the polyolefm fabric was dried at room temperature for 24 hours and then heat-treated at 38°C for 10 seconds. The nylon fabric was air dried for 24 hours before use. The fabrics were immersed into component B system first for 3 minutes, followed by curing at 80 °C for 3 minutes, and 150 °C for 3 minutes respectively. After forming a first nanolayer, fabrics were then immersed into component A, and dried at 150 °C for 3 minutes to make a layer of hydrophobic and olephobic coating . The two layer coating imparted the fabrics with good water and oil repellency.
Example 4
Average Particle Size
[0026] The silicon dioxide nanoparticle solution was diluted to 0.05 mass % with distilled water which had been passed through a 50μιη filter to obtain a sample. The average particle size of the sample was measured by dynamic light scattering method via a particle size measurement, system. The average particle size was found to be 180nm.
Example 5
Water repellency spray test
[0027] With respect to a test cloth, the water repellency was evaluated in accordance with the spray test method (AATCC standard test method No. 22). During the test, 250 ml of water was poured in a narrow stream at a 27 degree angle onto a fabric sample stretched on a 6-inch (15.2 cm) diameter plastic hoop, discharged from a funnel suspended 6 inches above the fabric sample. After removal of excess water, the fabric was visually scored by reference to published standards. A rating of 100 denotes no water penetration or surface adhesion; a rating of 90 denotes slight random sticking or wetting, and lower values indicate greater wetting. A rating of 0 indicates complete wetting. Testing results for water repellency rating were 95 for PET, 95 for nylon and 90 for cotton fabric respectively, indicating very good water repellency which results in the beading of water on the fabrics.
Example 6
Oil repellency test
[0028] The treated fabric samples were tested for oil repellency by a modification of AATCC standard test method No. 118. A series of organic liquids, identified below in Table 2 were introduced dropwise to the fabric samples. Beginning with the lowest numbered test liquid (Repellency rating No. 1), one drop (0.05mL volume) was placed on each of three locations at least 5 mm apart. The drops were observed for 30 seconds. If, at the end of this period, two of the three drops were still spherical to hemispherical in shape with no wicking around the drops, three drops of the next highest numbered liquid were placed on adjacent sites and similarly observed for 30 seconds. The procedure was continued until one of the test liquids results in two of the three drops failing to remain spherical to hemispherical, or wetting or wicking occurs. The oil-repellency rating of the fabric is the highest numbered test liquid for which two of the three drops remain spherical to hemispherical, with no wicking for 30 seconds.
Table 2:
Rating Oil repellency test liquid yL ,mN/m
1 Nujol >
2 65 % Nujof 28
3 n-hexadecane 27.6
4 n-tetradecane 26.7
5 n-dodecane 25.4
6 n-decane 23.9
7 n-octane 21.8
8 n-heptane 20.0 a Vol %In n-hexadecane
[0029] Via the testing, oil repellency rating was found to be 4 for PET, 4 for Nylon and 3 for cotton fabrics, indicating that the fabrics have good oil repellency rating.

Claims

What is claimed is:
A water and oil repellent coating for textile fabrics comprising:
a low surface energy portion comprising polyolefm having an R of 4 or less; and
a nanometer portion comprising nanoparticles.
2. The water and oil repellent coating of claim 1 , wherein the polyolefm comprises polymer of a formula
Figure imgf000013_0001
wherein Rls R2, R3 are each selected from H, CI and F, and the polymer has a molecular weight between 1000 and 100,000.
3. The water and oil repellent coating of claim 2, wherein the polyolefm is selected from the group consisting of tetrafluoropropene and pentafluoropropene compounds.
4. The water and oil repellent coating of claim 3, wherein said tetrafluoropropene and pentafluoropropene compounds are selected from the group consisting of: HFO- 1234yf, HFO-1234ze, HFO-1233zd, HFO-1234zf, HFO-1225, stereoisomers thereof, and combinations thereof.
The water and oil repellent coating of claim 1, wherein the nanoparticles comprise a nanoparticle selected from the group consisting of: silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, and combinations thereof.
6. The water and oil repellent coating of claim 5, wherein the nanoparticles consist essentially of nanoparticles selected from the group consisting of: silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, and combinations thereof.
7. A textile fabric coated with the water and oil repellent coating of claim 1, wherein the water and oil repellent coating comprises at least:
a first layer and a second layer, the first layer being adjacent to said textile fabric and comprising said nanometer portion,
a second layer comprising said low surface energy portion,
wherein said first layer is located between said textile fabric and said second layer.
8. The textile fabric according to claim 1, wherein the textile fabric is selected from the group consisting of cotton, cellulose , wool, silk, polyamide, polyester, polyolefm, polyacrylonitrile, and rayon.
9. A method of coating a textile fabric with the water and oil repellent coating according to claim 1, comprising the steps of:
coating at least a portion of the textile fabric with a solution comprising said nanoparticles; and
coating said portion with a solution comprising the polyolefm having an R of 4 or less.
10. The method according to claim 9, further comprising the step of preparing the
solution comprising the polyolefm.
11. The method according to claim 10, wherein preparing the solution comprises the steps of: polymerizing a fluoropolymer having a formula of
Figure imgf000015_0001
wherein Rls R2, R3 are each selected from H, CI and F, the fluoropolymer having a molecular weight between 1000 and 100,000;
precipitating the fluoropolymer; and
dissolving the precipitated fluoropolymer in at least one solvent.
12. The method according to claim 11, wherein the fluoropolymer is selected from the group consisting of tetrafluoropropene and pentafluoropropene compounds.
13. The method according to claim 12, wherein said tetrafluoropropene and
pentafluoropropene compounds are selected from the group consisting of: HFO- 1234yf, HFO-1234ze, HFO-1233zd, HFO-1234zf, HFO-1225, stereoisomers thereof, and combinations thereof.
14. The method according to claim 13, wherein the nanoparticles comprise a nanoparticle selected from the group consisting of: silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, and combinations thereof.
15. The method according to claim 14, wherein the nanoparticles consist essentially of nanoparticles selected from the group consisting of: silicon dioxide, zinc oxide, titanium dioxide, aluminum oxide, and combinations thereof.
PCT/CN2013/075321 2013-05-08 2013-05-08 Water and oil-repellent fluoropolymer having a short perfluorinated chain WO2014179946A1 (en)

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