EP0368338B1 - Water-and oil-repellent composition - Google Patents

Water-and oil-repellent composition Download PDF

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Publication number
EP0368338B1
EP0368338B1 EP19890120887 EP89120887A EP0368338B1 EP 0368338 B1 EP0368338 B1 EP 0368338B1 EP 19890120887 EP19890120887 EP 19890120887 EP 89120887 A EP89120887 A EP 89120887A EP 0368338 B1 EP0368338 B1 EP 0368338B1
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Prior art keywords
water
oil
glycerol
repellent
repellency
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EP19890120887
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German (de)
French (fr)
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EP0368338A2 (en
EP0368338A3 (en
Inventor
Yoshio Amimoto
Takashi Enomoto
Kazunori Hayashi
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Daikin Industries Ltd
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Daikin Industries Ltd
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    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
    • D06M13/144—Alcohols; Metal alcoholates
    • D06M13/148—Polyalcohols, e.g. glycerol or glucose
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/277—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof containing fluorine

Definitions

  • the present invention relates to an economical water- and oil-repellent composition having good water- and oil-repellency.
  • a water- and oil- repellent having a fluoroalkyl group has better properties than other conventional water-and oil-repellent, and is widely used. However, it is relatively expensive. In order to decrease the cost, it is proposed to replace a part of the water- and oil repellent having the fluoroalkyl group with a cheap acrylic acid base polymer or polyhydric alcohol such as sorbitol and lactose while keeping the water- and oil-repellency (cf. Japanese Patent Publication Nos. 22487/1963, 8579/1966 and 4160/1978). Although reduction of the cost is achieved to some extent while keeping the water- and oil- repellency, the above proposal is not satisfactory.
  • FR-A-22 56 281 discloses an oil and water repellent composition containing a fluoroalkyl polymer and glycerol compounds as surfactants.
  • GB-A-1 222 614 discloses a combination of fluorocarbons with an organic glycol as surfactant.
  • An object of the present invention is to provide an economical water- and oil-repellent composition having sufficient water- and oil-repellency.
  • a water- and oil-repellent composition which comprises a water- and oil-repellent composition which comprises a water- and oil-repellent which is a homopolymer of an acrylate or methacrylate having a fluoroalkyl group having 4 to 21 carbon atoms or a copolymer thereof with a monomer having no fluoroalkyl group and a glycerol compound selected from glycerol, an ester derivative of glycerol prepared by esterifying a hydroxyl group at the alpha-position with a monoalkane acid having 1 to 6 carbon atoms, an ether derivative of glycerol prepared by substituting a hydrogen of a hydroxyl group at the alpha-position with an alkyl group having 1 to 6 carbon atoms and polyglycerol, said polyglycerol having a melting point of lower than 70°C.
  • the ester derivative of glycerol is an ester prepared by esterifying a hydroxyl group at the ⁇ -position with a monoalkane acid having 1 to 6 carbon atoms, for example, glycerol ⁇ -monoacetate, glycerol ⁇ -monoformate and glycerol ⁇ -mono-n-hexanoate.
  • the ether derivative of glycerol is an ether prepared by substituting a hydrogen of a hydroxyl group at the ⁇ -position with an alkyl group having 1 to 6 carbon atoms, for example, glycerol ⁇ -monomethyl ether, glycerol ⁇ -monoethyl ether and glycerol ⁇ -monoisopropyl ether.
  • a ratio of the glycerol compound to the water- and oil-repellent is not critical and varies in a wide range dependent on other conditions such as the kinds of the water- and oil-repellent and the glycerol compound.
  • the amount of the glycerol compound is too large, the water-and oil-repellent composition has deteriorated properties.
  • the amount of the glycerol compound is too small, the cost is not reduced and the water- and oil-repellency is not improved.
  • the glycerol compound is usually used in an amount of 0.05 to 7 parts by weight, preferably 0.1 to 4 parts by weight per one part by weight of the water- and oil-repellent.
  • the amount of the water- and oil-repellent having the fluoroalkyl group is not limited.
  • the water- and oil-repellent having the fluoroalkyl group is usually used in an amount of 0.1 to 1.0 per 100 parts by weight of a medium.
  • the water- and oil-repellents are a homopolymer of an acrylate or methacrylate having a fluoroalkyl group having 4 to 21 carbon atoms and a copolymer thereof with a monomer having no fluoroalkyl group (cf. for example, Japanese Patent Publication 8068/1985).
  • the monomer having no fluoroalkyl group examples include ethylene, vinyl acetate, vinyl fluoride, vinyl chloride, vinylidene fluoride, vinylidene chloride, acrylonitrile, styrene, ⁇ -methylstyrene, p-methylstyrene, acrylic acid and alkyl esters thereof, methacrylic acid and alkyl esters thereof, acrylamide, diacetone acrylamide, methylol diacetone acrylamide, methylol diacetone methacrylamide, vinyl alkyl ether, vinyl alkyl ketone, butadiene, isoprene, chloroprene, glycidyl acrylate and maleic anhydride.
  • the monomer having no fluoroalkyl group is usually used in an amount of 0 to 75, preferably 20 to 65 parts by weight per 100 parts by weight of the polymer.
  • the homopolymer and copolymer of the above acrylate and methacrylate nay be prepared by bulk polymerization, solution polymerization or emulsion polymerization.
  • the emulsion polymerization is usually preferable. Accordingly, the medium is usually water.
  • the emulsion polymerization uses no specific procedure. For example, as described in Japanese Patent Publication No. 8068/1985, a mixture of monomers is emulsified in the presence of a surfactant and a polymerization initiator, and then polymerized at 50 to 100°C with stirring.
  • the initiator includes a peroxide, an azo compound and a persulfate.
  • the surfactant any of anionic, cationic and nonionic surfactants can be used. A mixture of at least one cationic surfactant and at least one nonionic surfactant is preferable.
  • composition of the present invention may include conventionally used additives, for example, a crosslinking agent, an antistatic agent, a dye fixing agent, an anticrease agent, a flame retardant, a mothproofing agent and the like, and it may include general-purpose organic solvents, for example, isopropanol and the like.
  • the water- and oil-repellent composition of the present invention may be applied on a material to be treated by conventionally known methods such as spraying or dipping.
  • the materials to be treated include natural and synthetic fibers and textiles.
  • the adsorption amount of the water- and oil-repellent to the material to be treated is preferably 0.01 to 2% by weight based on the material to be treated.
  • the ester or ether derivative of a polyhydric alcohol having more carbon atoms or hydroxyl groups than glycerol remains in a cloth in a large amount after the water- and oil-repellency treatment, and the water- and oil-repellency property decreases due to hydrophilic hydroxyl groups and lipophilic alkyl groups.
  • the treated cloth has deteriorated feeling.
  • An ester or ether derivative of a polyhydric alcohol or alcohol having fewer carbon atoms or hydroxyl groups than glycerol cannot increase the water- and oil-repellency.
  • the polyglycerol having the melting point of not lower than 70°C has the same defects as above.
  • the water- and oil-repellent composition according to the present invention is economical since the glycerol compound used as the blending component is more easily available than the conventional blending component which comprises the acrylic resin.
  • the water- and oil-repellency is usually insufficient. But, according to the present invention, the water- and oil-repellency is sufficient because of the use of the glycerol compound even if the water- and oil-repellent adheres to a cloth in a small amount.
  • the water- and oil-repellent composition was evaluated as follows:
  • the water repellency is expressed by the water repellency No. of Table 1 determined by the spray method according to JIS (Japanese Industrial Standard) L-1092.
  • Oil repellency is expressed by the oil repellency No. of Table 2 determined by dropping several drops (diameter: about 4 mm) of a test solvent on two positions of a surface of a test cloth and observing whether the drops are held on the surface for 30 seconds or not.
  • the superscript "+" to the water repellency No. represents that the result is slightly better than said water repellency No.
  • Resistance to washing is expressed by the water-and oil-repellency Nos. which are determined after carrying out five cycles each consisting of washing a cloth treated with the water- and oil-repellent composition at 40°C in water containing 0.3 % by weight of detergent (Zabu-koso XK, manufactured by Kao) with a bath ratio of 1:40 (cloth:washing liquid (g:g)) for 5 minutes by using a domestic washing machine followed by rinsing the cloth for 15 minutes, dehydrating it and drying it at room temperature.
  • detergent Zabu-koso XK, manufactured by Kao
  • Water- and oil-repellency Nos. which are determined by washing a cloth treated with the water- and oil-repellent composition at 30°C in tetrachloroethylene by using a Launder-O-meter followed by drying at room temperature and then measuring the water- and oil-repellency.
  • a water- and oil-repellent used in the water- and oil-repellent composition of the present invention was prepared as follows:
  • the emulsion was mixed with the blending components as shown in Table 3 to prepare water- and oil-repellent compositions.
  • Test cloths were a polyester finished yarn woven fabric (hereinafter referred to as PE) and a nylon taffeta fabric (hereinafter referred to as N), and were dipped in the above composition for one minute and squeezed between two rolls so as to adjust the water content at 90 % and 50 %, respectively. Then, they were dried at 110°C for three minutes, PE was thermally treated at 180°C for 40 seconds and N was thermally treated at 170°C for one minute to impart the water- and oil-repellency. The water- and oil-repellency of the treated cloths were measured. The results are shown in Table 4.
  • PE polyester finished yarn woven fabric
  • N nylon taffeta fabric

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

  • The present invention relates to an economical water- and oil-repellent composition having good water- and oil-repellency.
  • A water- and oil- repellent having a fluoroalkyl group has better properties than other conventional water-and oil-repellent, and is widely used. However, it is relatively expensive. In order to decrease the cost, it is proposed to replace a part of the water- and oil repellent having the fluoroalkyl group with a cheap acrylic acid base polymer or polyhydric alcohol such as sorbitol and lactose while keeping the water- and oil-repellency (cf. Japanese Patent Publication Nos. 22487/1963, 8579/1966 and 4160/1978). Although reduction of the cost is achieved to some extent while keeping the water- and oil- repellency, the above proposal is not satisfactory.
  • FR-A-22 56 281 discloses an oil and water repellent composition containing a fluoroalkyl polymer and glycerol compounds as surfactants. GB-A-1 222 614 discloses a combination of fluorocarbons with an organic glycol as surfactant.
  • An object of the present invention is to provide an economical water- and oil-repellent composition having sufficient water- and oil-repellency.
  • This and other objects of the present invention are achieved by a water- and oil-repellent composition which comprises a water- and oil-repellent composition which comprises a water- and oil-repellent which is a homopolymer of an acrylate or methacrylate having a fluoroalkyl group having 4 to 21 carbon atoms or a copolymer thereof with a monomer having no fluoroalkyl group and a glycerol compound selected from glycerol, an ester derivative of glycerol prepared by esterifying a hydroxyl group at the alpha-position with a monoalkane acid having 1 to 6 carbon atoms, an ether derivative of glycerol prepared by substituting a hydrogen of a hydroxyl group at the alpha-position with an alkyl group having 1 to 6 carbon atoms and polyglycerol, said polyglycerol having a melting point of lower than 70°C.
  • The ester derivative of glycerol is an ester prepared by esterifying a hydroxyl group at the α-position with a monoalkane acid having 1 to 6 carbon atoms, for example, glycerol α-monoacetate, glycerol α-monoformate and glycerol α-mono-n-hexanoate. The ether derivative of glycerol is an ether prepared by substituting a hydrogen of a hydroxyl group at the α-position with an alkyl group having 1 to 6 carbon atoms, for example, glycerol α-monomethyl ether, glycerol α-monoethyl ether and glycerol α-monoisopropyl ether.
  • In the composition of the present invention, a ratio of the glycerol compound to the water- and oil-repellent is not critical and varies in a wide range dependent on other conditions such as the kinds of the water- and oil-repellent and the glycerol compound. When the amount of the glycerol compound is too large, the water-and oil-repellent composition has deteriorated properties. When the amount of the glycerol compound is too small, the cost is not reduced and the water- and oil-repellency is not improved. Accordingly, the glycerol compound is usually used in an amount of 0.05 to 7 parts by weight, preferably 0.1 to 4 parts by weight per one part by weight of the water- and oil-repellent.
  • The amount of the water- and oil-repellent having the fluoroalkyl group is not limited. The water- and oil-repellent having the fluoroalkyl group is usually used in an amount of 0.1 to 1.0 per 100 parts by weight of a medium.
  • The water- and oil-repellents are a homopolymer of an acrylate or methacrylate having a fluoroalkyl group having 4 to 21 carbon atoms and a copolymer thereof with a monomer having no fluoroalkyl group (cf. for example, Japanese Patent Publication 8068/1985).
  • Preferable acrylate and methacrylate having the fluoroalkyl group are as follows:
       Rf(CH₂)mOCOCR¹=CH₂ and
       RfSO₂NR²(CH₂)mOCOR¹=CH₂
    wherein Rf is a perfluoroalkyl group having 4 to 21 carbon atoms, R¹ is hydrogen or a methyl group, R² is an alkyl group having 1 to 10 carbon atoms, and m is an integer of 1 to 10.
  • Specific examples of the acrylate and methacrylate having the fluoroalkyl group are as follows:
       CF₃(CF₂)₇(CH₂)₁₁OCOCH=CH₂
       CF₃(CF₂)₄CH₂OCOC(CH₃)=CH₂
       CF₃(CF₂)₆(CH₂)₂OCOC(CH₃)=CH₂
       CF(CF₃)₂(CF₂)₆(CH₂)₃OCOCH=CH₂
       CF(CF₃)₂(CF₂)₁₀(CH₂)₃OCOCH=CH₂
       CF₃(CF₂)₇SO₂N(C₃H₇)(CH₂)₂OCOCH=CH₂
       CF₃(CF₂)₇SO₂N(CH₃)(CH₂)₂OCOC(CH₃)=CH₂
       CF(CF₃)₂(CF₂)₆CH₂CH(OH)CH₂OCOCH=CH₂
       CF(CF₃)₂(CF₂)₆CH₂CH(OCOCH₃)OCOC(CH₃)=CH₂
       CClF₂(CF₂)₁₀CH₂OCOC(CH₃)=CH₂
       H(CF₂)₁₀CH₂OCOCH=CH₂
    In addition to the above, the monomer having the fluoroalkyl group of the formula:



            CF(CF₃)(CClF₂)(CF₂)₇CONHCOOCH=CH₂



    can be used alone or in addition to the above methacrylate or acrylate.
  • Specific examples of the monomer having no fluoroalkyl group are ethylene, vinyl acetate, vinyl fluoride, vinyl chloride, vinylidene fluoride, vinylidene chloride, acrylonitrile, styrene, α-methylstyrene, p-methylstyrene, acrylic acid and alkyl esters thereof, methacrylic acid and alkyl esters thereof, acrylamide, diacetone acrylamide, methylol diacetone acrylamide, methylol diacetone methacrylamide, vinyl alkyl ether, vinyl alkyl ketone, butadiene, isoprene, chloroprene, glycidyl acrylate and maleic anhydride. The monomer having no fluoroalkyl group is usually used in an amount of 0 to 75, preferably 20 to 65 parts by weight per 100 parts by weight of the polymer.
  • The homopolymer and copolymer of the above acrylate and methacrylate nay be prepared by bulk polymerization, solution polymerization or emulsion polymerization. The emulsion polymerization is usually preferable. Accordingly, the medium is usually water. The emulsion polymerization uses no specific procedure. For example, as described in Japanese Patent Publication No. 8068/1985, a mixture of monomers is emulsified in the presence of a surfactant and a polymerization initiator, and then polymerized at 50 to 100°C with stirring. The initiator includes a peroxide, an azo compound and a persulfate. As the surfactant, any of anionic, cationic and nonionic surfactants can be used. A mixture of at least one cationic surfactant and at least one nonionic surfactant is preferable.
  • The composition of the present invention may include conventionally used additives, for example, a crosslinking agent, an antistatic agent, a dye fixing agent, an anticrease agent, a flame retardant, a mothproofing agent and the like, and it may include general-purpose organic solvents, for example, isopropanol and the like.
  • The water- and oil-repellent composition of the present invention may be applied on a material to be treated by conventionally known methods such as spraying or dipping.
  • The materials to be treated include natural and synthetic fibers and textiles. The adsorption amount of the water- and oil-repellent to the material to be treated is preferably 0.01 to 2% by weight based on the material to be treated.
  • When a polyhydric alcohol, an ester or ether derivative of the polyhydric alcohol, or polyglycerol having the melting point of not lower than 70°C which is not included in the glycerol compound of the present invention is used in the water- and oil-repellent composition, an effect is observed to some extent but various defects arise. For example, the ester or ether derivative of a polyhydric alcohol having more carbon atoms or hydroxyl groups than glycerol remains in a cloth in a large amount after the water- and oil-repellency treatment, and the water- and oil-repellency property decreases due to hydrophilic hydroxyl groups and lipophilic alkyl groups. In addition, the treated cloth has deteriorated feeling. An ester or ether derivative of a polyhydric alcohol or alcohol having fewer carbon atoms or hydroxyl groups than glycerol cannot increase the water- and oil-repellency. The polyglycerol having the melting point of not lower than 70°C has the same defects as above.
  • The water- and oil-repellent composition according to the present invention is economical since the glycerol compound used as the blending component is more easily available than the conventional blending component which comprises the acrylic resin.
  • In addition, when the conventional water- and oil-repellent is added in a small amount, the water- and oil-repellency is usually insufficient. But, according to the present invention, the water- and oil-repellency is sufficient because of the use of the glycerol compound even if the water- and oil-repellent adheres to a cloth in a small amount.
  • The present invention will be illustrated by following Examples. The Examples, of course, do not restrict the present invention.
  • The water- and oil-repellent composition was evaluated as follows:
       The water repellency is expressed by the water repellency No. of Table 1 determined by the spray method according to JIS (Japanese Industrial Standard) L-1092. Oil repellency is expressed by the oil repellency No. of Table 2 determined by dropping several drops (diameter: about 4 mm) of a test solvent on two positions of a surface of a test cloth and observing whether the drops are held on the surface for 30 seconds or not. The superscript "+" to the water repellency No. represents that the result is slightly better than said water repellency No.
  • Feeling is evaluated by measuring the rigidity and softness of the cloth by the Handle-O-meter method according to JIS L-1096.
  • Resistance to washing is expressed by the water-and oil-repellency Nos. which are determined after carrying out five cycles each consisting of washing a cloth treated with the water- and oil-repellent composition at 40°C in water containing 0.3 % by weight of detergent (Zabu-koso XK, manufactured by Kao) with a bath ratio of 1:40 (cloth:washing liquid (g:g)) for 5 minutes by using a domestic washing machine followed by rinsing the cloth for 15 minutes, dehydrating it and drying it at room temperature.
  • Resistance to dry cleaning is expressed by the water- and oil-repellency Nos. which are determined by washing a cloth treated with the water- and oil-repellent composition at 30°C in tetrachloroethylene by using a Launder-O-meter followed by drying at room temperature and then measuring the water- and oil-repellency. Table 1
    Water repellency No. State
    100 No wet on the surface
    90 Slight wet on the surface
    80 Drop like wet on the surface
    70 Considerable wet on the surface
    50 Wet over the whole surface
    0 Complete wet of the surface and backface
    Table 2
    Oil repellency No. Test solvent Surface tension (dyne/cm, 25°C)
    8 n-Heptane 20.0
    7 n-Octane 21.3
    6 n-Decane 23.5
    5 n-Dodecane 25.0
    4 n-Tetradecane 26.7
    3 n-Hexadecane 27.3
    2 n-Hexadecane/Nujol (35/65 by weight) 29.6
    1 Nujol 31.2
    0 Nujol penetrated
    • Examples 1 to 4 and Comparative Examples 1 to 3
  • A water- and oil-repellent used in the water- and oil-repellent composition of the present invention was prepared as follows:
  • The compound (60 g) of the formula:



            (CF₃)₂CF(CF₂CF₂)nCH₂CH₂OOCCH=CH₂



    (mixture of n = 3, 4 and 5 in a weight ratio of 5:3:1), C₁₈H₃₇OOCCH=CH₂ (38 g), CH₂=CHCOOCH₂CH(OH)CH₂Cl (2 g), pure water (250 g), acetone (50 g), n-dodecyl mercaptan (0.2 g) dimethylalkylamine acetate salt (3 g) and polyoxyethylenealkylphenol (3 g) were charged in a flask, and stirred at 60°C for one hour under a nitrogen stream. A solution of azobisisobutylamidine hydrochloride (1 g) in water (10 g) was added and the copolymerization was carried out while stirring at 60°C for 5 hours under the nitrogen stream. According to a gas chromatography, a conversion of copolymerization was not lower than 99%. From this conversion, a ratio of the repeating units of the resultant copolymer was found to be substantially almost the same as a ratio of the charged monomers. The resultant emulsion contained the copolymer in the solid content of 25 %.
  • The emulsion was mixed with the blending components as shown in Table 3 to prepare water- and oil-repellent compositions.
  • Test cloths were a polyester finished yarn woven fabric (hereinafter referred to as PE) and a nylon taffeta fabric (hereinafter referred to as N), and were dipped in the above composition for one minute and squeezed between two rolls so as to adjust the water content at 90 % and 50 %, respectively. Then, they were dried at 110°C for three minutes, PE was thermally treated at 180°C for 40 seconds and N was thermally treated at 170°C for one minute to impart the water- and oil-repellency. The water- and oil-repellency of the treated cloths were measured. The results are shown in Table 4.
  • As is clear from Table 4, when the glycerol compound of the present invention is added to the water- and oil-repellent composition, good water- and oil-repellency is achieved. Table 3
    Example No. Test cloth Adhesion of repellent to fabric (wt%) Blending component Adhesion of blending component to fabric (wt%)
    1 PE 0.03 Glycerol 0.015
    N 0.10 0.05
    2 PE 0.03 Glycerol α-monomethyl ether 0.015
    N 0.10 0.05
    3 PE 0.03 Glycerol α-monoacetate 0.015
    N 0.10 0.05
    4 PE 0.03 Polyglycerol (melting point: 30°C) (molecular weight: 170) 0.015
    N 0.10 0.05
    Comp.1 PE 0.03 - -
    N 0.10 -
    Comp.2 PE 0.03 Sorbitol 0.015
    N 0.10 0.05
    Comp.3 PE 0.03 Polyglycerol (melting point: >70°C) (molecular weight: 1000) 0.015
    N 0.10 0.05
    Figure imgb0001

Claims (2)

  1. A water- and oil-repellent composition which comprises a water- and oil-repellent which is a homopolymer of an acrylate or methacrylate having a fluoroalkyl group having 4 to 21 carbon atoms or a copolymer thereof with a monomer having no fluoroalkyl group and a glycerol compound selected from glycerol, an ester derivative of glycerol prepared by esterifying a hydroxyl group at the alpha-position with a monoalkane acid having 1 to 6 carbon atoms, an ether derivative of glycerol prepared by substituting a hydrogen of a hydroxyl group at the alpha-position with an alkyl group having 1 to 6 carbon atoms and polyglycerol, said polyglycerol having a melting point of lower than 70°C.
  2. The water- and oil-repellent composition according to claim 1, wherein the composition contains the glycerol compound in an amount of 0.05 to 7 parts by weight per one part by weight of the water- and oil-repellent.
EP19890120887 1988-11-11 1989-11-10 Water-and oil-repellent composition Expired - Lifetime EP0368338B1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP28637688 1988-11-11
JP286376/88 1988-11-11
JP31913088A JP2503612B2 (en) 1988-11-11 1988-12-16 Water and oil repellent composition
JP319130/88 1988-12-16

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EP0368338A2 EP0368338A2 (en) 1990-05-16
EP0368338A3 EP0368338A3 (en) 1990-08-08
EP0368338B1 true EP0368338B1 (en) 1995-02-22

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DE3935859A1 (en) * 1989-10-27 1991-05-02 Bayer Ag DISPERSIONS OF PERFLUORAL CYL GROUPS CONTAINING COPOLYMERISATE
DE4113894A1 (en) * 1991-04-27 1992-10-29 Bayer Ag WAFERRED DISPERSIONS OF COPOLYMERIZES CONTAINING PERFLUOROAL CYL GROUPS, THEIR PREPARATION AND USE
JPWO2021235452A1 (en) * 2020-05-20 2021-11-25

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NL6815430A (en) * 1967-11-02 1969-05-06
US3960797A (en) * 1973-12-28 1976-06-01 Pennwalt Corporation Water-in-oil emulsions of fluoroalkyl polymer, chlorinated alkane solvent and non-ioinic surfactant

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EP0368338A2 (en) 1990-05-16
DE68921289D1 (en) 1995-03-30
JPH02229879A (en) 1990-09-12
DE68921289T2 (en) 1995-07-27
JP2503612B2 (en) 1996-06-05
EP0368338A3 (en) 1990-08-08

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