WO1998020170A1 - Utilisation de copolymeres amphiphiles contenant un monomere fluore pour rendre un cuir impermeable - Google Patents

Utilisation de copolymeres amphiphiles contenant un monomere fluore pour rendre un cuir impermeable Download PDF

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Publication number
WO1998020170A1
WO1998020170A1 PCT/US1997/018386 US9718386W WO9820170A1 WO 1998020170 A1 WO1998020170 A1 WO 1998020170A1 US 9718386 W US9718386 W US 9718386W WO 9820170 A1 WO9820170 A1 WO 9820170A1
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Prior art keywords
leather
amphiphilic copolymer
group
recurring units
alkyl group
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PCT/US1997/018386
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English (en)
Inventor
Dirk M. Coppens
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Minnesota Mining And Manufacturing Company
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Application filed by Minnesota Mining And Manufacturing Company filed Critical Minnesota Mining And Manufacturing Company
Priority to US09/297,814 priority Critical patent/US6294103B1/en
Priority to BR9712754-0A priority patent/BR9712754A/pt
Priority to JP52140298A priority patent/JP3911549B2/ja
Priority to AU48998/97A priority patent/AU4899897A/en
Publication of WO1998020170A1 publication Critical patent/WO1998020170A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C14—SKINS; HIDES; PELTS; LEATHER
    • C14C—CHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C9/00—Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes

Definitions

  • This invention relates to leather manufacture and the use of fluoroalkyl group containing amphiphilic copolymers therein. More in particular, the invention relates to fluoroalkyl group containing amphiphilic copolymers and their use in a waterproofness imparting composition for leather substrates. In another aspect, the invention relates to a method for imparting a high degree of waterproofness to leather substrates and to the resulting treated leather substrates.
  • the treatment of hides and skins to form leather involves a number of interdependent chemical and mechanical operations. These operations may be divided into a sequence of "wet end” steps followed by a sequence of “dry” steps. A description of each of these operations is provided in Fundamentals of Leather Manufacturing, Prof. Dr. Heidemann (Eduard Roether KG, 1993).
  • the primary tanning operation involves the treatment of the hide to preserve it and form useful leather. Chrome tanning salts are well known and widely used for this purpose. Chrome-tanned hides or skins are known in the art as 'wet blue leather'. In order to produce a uniform piece of leather with the required physical and aesthetic properties, a second tanning step, known as 'retanning', is employed.
  • Retanning can be accomplished using a variety of naturally derived materials including extracts from vegetables or plants, and synthetic tanning agents known as "syntans", or combinations thereof. After or during retanning, the leather can be colored and fatliquored.
  • the present invention relates to the wet end operations which take place after primary tanning, namely retanning and fatliquoring.
  • EP-A-372 746 discloses a method and process for treating leather utilizing selected amphiphilic copolymers for improving the strength, temper and water resistance of the leather.
  • the amphiphilic copolymers are formed from a predominant amount of at least one hydrophobic monomer and a minor amount of at least one copolymerizable hydrophilic monomer.
  • the application states that the process may be particularly useful as a one step substitute for conventional retanning and fatliquoring treatment steps.
  • EP-A-682 044 discloses copolymers comprising ethylenically unsaturated dicarboxylic acid anhydrides, long chain olefins and fluorolefins. Leathers treated with these polymers are shown to yield good waterproofness results according to the Bally-Penetrometer test.
  • U.S. Patent No. 5,124,181 discloses copolymers which contain (a) from 50 to 90% by weight of Cg to C40 alkyl methacrylates, vinyl esters of C 8 to C 40 carboxylic acids or mixtures thereof and (b) from 10 to 50% by weight of monoethylenically unsaturated C 3 to C 12 carboxylic acids, monoethylenically unsaturated dicarboxylic anhydrides, monoesters or monoamides of monoethylenically unsaturated C to C ⁇ 2 dicarboxylic acids, amides of C 3 to C ⁇ 2 monocarboxylic acids or mixtures thereof as copolymerized units and which have molecular weights of from 500 to 30,000.
  • the copolymers are used in at least partially neutralized form in aqueous solution or dispersion for making leather and furs water repellent.
  • WO 94/01587 discloses water-dispersible and/or water-emulsifiable co- oligomers containing (a) fatty crotonates; (b) radically copolymerizable, hydrophilic, ethylenically unsaturated acids and/or their anhydrides; and possibly (c) minor amounts of other copolymerizable comonomers. These co-oligomers are used as amphiphilic agents for greasing leather and pelts.
  • a method of treating leather comprising contacting a leather, in particular a tanned leather, with an amphiphilic copolymer, said amphiphilic copolymer comprising the following recurring units: O
  • R represents a fluorinated alkyl group having at least 3 carbon atoms
  • Q and Q' each independently represent an organic linking group or other chemical linkage
  • R 1 and R 2 each independently represent hydrogen or a C C 4 alkyl group
  • R h represents a hydrocarbon group having at least 8 carbon atoms and optionally containing 1 to 3 substituents; and a recurring unit comprising at least one carboxylic acid group or salt thereof.
  • the present invention further provides amphiphilic copolymers as defined above and aqueous compositions comprising them.
  • the present invention provides a use of an above defined amphiphilic copolymer in treating leather to provide waterproofness thereto. Also the present invention provides leathers comprising an amphiphilic copolymer as defined above.
  • the present invention provides a method for making above defined amphiphilic copolymers.
  • the invention simplifies the manufacture of waterproof leather by providing in one step the desired properties normally obtained by separate, conventional wet end retanning and fatliquoring steps.
  • a particularly preferred amphiphilic copolymer for use in connection with this invention is a copolymer wherein the recurring unit having at least one carboxylic acid group or salt thereof corresponds to the following formula (III): O
  • R >3 ⁇ represents hydrogen or a Ci to C 4 alkyl group
  • Y represents an organic linking group or other chemical linkage and; M represents a hydrogen or a cation.
  • a fluorinated alkyl group Rf in the fluorochemical containing recurring unit according to formula (I), is preferably a fluorinated, stable, inert, preferably saturated, non-polar, monovalent alkyl group. It can be straight chain, branched chain, or cyclic or combinations thereof. It can contain heteroatoms, bonded only to carbon atoms, such as oxygen, divalent or hexavalent sulfur, or nitrogen.
  • R f is preferably a fully-fluorinated alkyl group, but hydrogen or chlorine atoms can be present as substituents but preferably not more than one atom of either is present for every two carbon atoms.
  • the Rf group has at least 3 carbon atoms, preferably 3 to 14 carbon atoms, and more preferably at least 6 carbon atoms.
  • Rf preferably contains about 40% to about 80% fluorine by weight, more preferably about 50% to about 78% fluorine by weight.
  • the terminal portion of the Rf radical is preferably a perfluorinated moiety, preferably containing at least 7 fluorine atoms, e.g., CF 3 CF 2 CF 2 -, (CF 3 ) 2 CF-, F 5 SCF 2 -.
  • Preferred R f groups are fully or substantially fluorinated and are preferably those perfluorinated alkyls according to the formula C n F 2n+ ⁇ - where n is 3 to 14.
  • Linking groups Q, Q' and Y in the above formulas (I) to (III) preferably contain from 1 to about 20 carbon atoms. They can optionally contain oxygen, nitrogen, or sulfur-containing groups or a combination thereof, and are preferably free of functional groups that substantially interfere with free-radical polymerization (e.g., polymerizable olefinic double bonds, thiols, easily abstracted hydrogen atoms such as cumyl hydrogens, and other such functionality known to those skilled in the art).
  • functional groups e.g., polymerizable olefinic double bonds, thiols, easily abstracted hydrogen atoms such as cumyl hydrogens, and other such functionality known to those skilled in the art).
  • linking groups include straight chain, branched chain or cyclic alkylene, arylene, aralkylene, oxy, oxo, hydroxy, thio, sulfonyl, sulfoxy, amino, imino, sulfonamido, carboxyamido, carbonyloxy, urethanylene, ureylene, and combinations thereof such as sulfonamidoalkylene.
  • Preferred linking groups for Q and Q' include -(CH 2 CH 2 ) k O- and -SO 2 N(R)CH 2 CH 2 - wherein k is 1 or 2 and R is a Ci to C 4 -alkyl group.
  • a preferred linking group Y is an aliphatic or aromatic linking group.
  • Rh groups for use in connection with the present invention are hydrocarbon groups having at least 8 carbons and more preferably at least 12 carbon atoms. These hydrocarbon groups can contain 1 to 3 substituents such as e.g., a halogen, an amino group, an aryl group, an alkoxy group, etc. More preferably, however, the hydrocarbon group is unsubstituted and preferably saturated. Particularly preferred Rh-groups for use in this invention are unsubstituted linear or branched alkyl groups preferably having at least 12 carbon atoms. Hydrocarbon groups R h for use in this invention may also contain cyclo aliphatic groups such as, e.g., a cyclohexane.
  • Suitable cations M for use in the present invention include monovalent ions such as e.g. sodium ion, potassium ion or ammonium ion. It is also possible to use a mixture of two or more of such cations.
  • amphiphilic copolymers used in connection with the present invention can be prepared by free radical polymerisation, e.g.,. by solution- or emulsion- polymerization techniques of monomers (a), (b) and an ethylenically unsaturated monomer having a carboxylic acid group , a salt of a carboxylic acid group or a precursor of a carboxylic acid group using a free radical initiator: O
  • the ethylenically unsaturated monomer corresponds to the following formula (c): O
  • MOOC-Y-O-C-CR 3 CH 2 (c)
  • R f , R h , R 1 ' 2 ' 3 , Q, Q ⁇ Y and M have the same meaning as defined above.
  • Useful free radical initiators include azo compounds, such as azo-isobutyronitrile and azo-2-cyanovaleric acid, hydroperoxides such as cumene, t-butyl and t-amyl hydroperoxide, dialkyl peroxides such as di-t-butyl and dicumylperoxide, peroxyesters such as t- butylperbenzoate and di-t-butylperoxy phthalate, diacylperoxides such as benzoyl peroxide and lauroyl peroxide.
  • azo compounds such as azo-isobutyronitrile and azo-2-cyanovaleric acid
  • hydroperoxides such as cumene, t-butyl and t-amyl hydroperoxide
  • dialkyl peroxides such as di-t-but
  • chain transfer agents can be used in order to control the molecular weight of the polymer.
  • examples include mercaptoethanol, mercaptoacetic acid, stearylmercaptane, tert-dodecylmercaptane and the like.
  • the ethylenically unsaturated monomer comprises a precursor of a carboxylic acid group such as e.g. an anhydride
  • the precursor can be converted to a carboxylic acid group or salt thereof during or subsequent to the free radical polymerisation.
  • Fluorochemical monomers and in particular (meth)acrylate monomers corresponding to formula (a) and methods for the preparation thereof are known and disclosed, e.g., in U.S. Patent No. 2,803,615.
  • Examples of such compounds include general classes of fluorochemical acrylates or methacrylates containing fluorinated sulfonamido groups, acrylates or methacrylates derived from telomer alcohols, acrylates or methacrylates derived from fluorochemical carboxylic acids and acrylates or methacrylates as disclosed in EP 526976.
  • Preferred examples of fluorochemical (meth)acrylates include :
  • R a methyl or ethyl.
  • Suitable monomers according to formula (b) for preparing amphiphilic copolymers in accordance with this invention include long chain Cg to C o alkyl acrylates and Cg to C 4 o alkyl methacrylates.
  • suitable compounds of this type are 2-ethylhexyl (meth)acrylate, n-decyl (meth)acrylate, dodecyl (meth)acrylate, isotridecyl (meth)acrylate, tetradecyl (meth)acrylate, Ci 6 i 8 tallow fatty alcohol (meth)acrylate, octadecyl (meth)acrylate, palmityl (meth)acrylate, n- eicosyl (meth)acrylate.
  • Suitable ethylenically unsaturated monomers having a carboxylic acid group, a salt of a carboxylic acid group or a precursor of a carboxylic acid group for preparing amphiphilic copolymers in accordance with this invention include dicarboxylic acid anhydrides, such as, e.g., maleic acid anhydride, or monoethylenically unsaturated C 3 to C ⁇ carboxylic acids. Examples include acrylic acid, methacrylic acid, 2-carboxyethylacrylate, monomethacryloyloxyethyl phthalate.
  • an amphiphilic copolymer in connection with this invention consists of recurring units according to formulas (I) and (II) and recurring units having a carboxylic acid group or salt thereof.
  • the final leather properties can be selected as desired by balancing contents of carboxylic acid (or salt), the fluorine content and the long chain alkyl group content. Increasing the free acid (and salt) content will increase water solubility of an amphiphilic copolymer in connection with this invention and therefore also the hydrophilicity thereof. On the other hand, if the carboxylic acid content is low the copolymer may not adequately penetrate the leather structure and/or may not bind sufficiently into the leather. In accordance with the present invention it is highly preferred to incorporate sufficient free carboxylic acid (or salt) groups in the polymer in order to provide the polymer with sufficient crosslinking possibilities with the tanned leather, so as to irreversibly bond the polymer to the leather.
  • a particularly preferred amount of recurring units having at least one carboxylic acid group or salt thereof, in particular recurring units according to formula (III), is between 5% and 60% by weight and more preferably between 10% and 50% by weight based on the total weight of the recurring units according to formulas (I) and (II) and the recurring units having at least one carboxylic acid group or salt thereof.
  • the long chain alkyl group content is preferably high enough to assure the leather is lubricated properly. On the other hand the long chain alkyl group content is preferably such that there is still a desired level of penetration into the leather.
  • the amount of recurring units according to formula (II) is at least 20% by weight of the total weight of the recurring units according to formulas (I) and (II) and the recurring units having at least one carboxylic acid group or salt thereof.
  • fatty alkyl groups having an average chain length of at least 12 carbon atoms are preferably present in an amount of above 20% by weight.
  • the content of recurring units according to formula (I) is preferably at least 1% by weight, more preferably at least 5% by weight and most preferably at least 10 % by weight based on the total weight of the recurring units according to formulas (I) and (II) and the recurring units having at least one carboxylic acid group or salt thereof. If the fluorine content is too low, the water repellency of the leather may be insufficient. On the other hand, if the fluorine content is too high, the leather may become undesirable hard.
  • An amphiphilic copolymer in connection with the present invention is preferably used as an aqueous composition, in particular an aqueous dispersion in water. If the copolymer is made by solution polymerization, it can be dispersed in water, through vigorously mixing the solution polymer with water. A solvent free dispersion can be obtained by subsequent distillation of the polymerization solvent. A partial or complete neutralization of the acid groups present in the copolymer can be obtained by means of a suitable base, such as e.g. sodium hydroxide, potassium hydroxide, ammonium hydroxide or triethanolamine and the like.
  • a suitable base such as e.g. sodium hydroxide, potassium hydroxide, ammonium hydroxide or triethanolamine and the like.
  • a leather such as a tanned hide is contacted with an aqueous composition, preferably an aqueous dispersion, comprising amphiphilic copolymer.
  • Amphiphilic copolymer aqueous dispersions in accordance with the invention are suitable for the treatment of all conventional tanned hides, in particular hides tanned with mineral tanning agents, such as chromium(III)salts.
  • the tanned hides are usually neutralized before treatment. They may be dyed before treatment. However, dyeing may also be carried out after a waterproofing treatment in accordance with this invention.
  • the tanned hides can be treated with an aqueous dispersion comprising an amphiphilic copolymer in accordance with the invention preferably in an aqueous liquor obtained by diluting the amphiphilic copolymer dispersions with water, at a pH of from 3 to 10, preferably from 5 to 8, and at from 20°C to 70°C, preferably from 40°C to 60°C.
  • the amount of the amphiphilic copolymer dispersion applied to the leather in accordance with this invention is chosen so that sufficiently high or desirable water repellency is imparted to the substrate, said amount usually being between 0.1% and 30% by weight, preferably between 0.5% and 15% by weight, based on the shaved weight of the leather or the wet weight of the hide or wet blue leather.
  • the amount which is sufficient to impart desired repellency can be determined empirically and can be increased as necessary or desired.
  • the treatment is effected, for example, by drumming. After the treatment with the aqueous dispersion described above, the pH of the treatment liquor is preferably brought to 3-5, preferably 3.3-4, by addition of an acid in particular an organic acid, such as formic acid.
  • aqueous compositions according to this invention In order to increase repellency properties and the durability thereof and to aid in the application of an aqueous composition according to the present invention to a leather substrate to be treated therewith, it may be advantageous to incorporate into an aqueous composition according to this invention, one or more other substances such as oil and/or water repellent compositions and/or siloxane softening agents. Also other additives such as conventional leather finishing agents, e.g., retanning, fatliquoring agents can be added.
  • Particularly preferred aqueous compositions for use in connection with the present invention include a water and/or oil repellent composition in addition to the amphiphilic copolymer in connection with the present invention.
  • Preferred water and/or oil repellent compositions for use in this invention are fluorochemical compositions comprising a mixture of normally solid compounds and/or polymers, each of the compounds having at least two fluoroaliphatic groups and a large hydrocarbon moiety and each of the polymers having at least one fluoroaliphatic group and a plurality of said hydrocarbon moiety.
  • Particularly preferred are compositions comprising compounds that are fluoroaliphatic esters of dimer acids and/or trimer acids. Examples of fluorochemical compositions that can be used in an aqueous composition in accordance with this invention are described in WO 93/10085.
  • the so treated leather sample was horsed-up overnight, dried at 60°C during 60 min, staked in the conventional manner and conditioned at room temperature during 2 weeks.
  • the leather substrates used for the evaluation of the treatment according to the invention are all commercially available and are listed below:
  • the water resistance of the leathers was tested according to
  • the water repellency (WR) of a treated substrate was measured using a series of water-isopropyl alcohol test liquids and was expressed in terms of the
  • WR "WR" rating of the treated substrate.
  • the WR rating corresponds to the most penetrating test liquid which does not penetrate or wet the substrate surface after 15 seconds exposure.
  • the spray rating of a treated substrate is a value indicative of the dynamic repellency of the treated substrate to water that impinges on the treated substrate.
  • the repellency is measured by Standard Test Number 22, published in the 1985 Technical Manual and Yearbook of the American Association of Textile Chemists and Colorists (AATCC), and is expressed in terms of 'spray rating' of the tested substrate.
  • the spray rating is obtained by spraying 250 ml water on the substrate from a distance of 15 cm.
  • the wetting pattern is visually rated using a 0 to 100 scale, where 0 means complete wetting and 100 means no wetting at all.
  • Oil Repellency The oil repellency of a treated substrate is measured by the American
  • a Bally Penetrometer test was done according to DIN 53338.
  • a Bally Penetrometer Model 5023 (a standardized dynamic testing machine for shoe upper leather) was used.
  • the test piece was alternatively buckled and stretched by the machine, like an upper leather in actual use, while in contact with water on one side.
  • the values measured in this test are:
  • weight percent increase of the test piece caused by water absorption during the test is typically greater than 100% after one hour.
  • the repellency of an abraded treated substrate is measured on 5cmxl2.5cm test pieces of treated substrate which has been abraded using 10 back and forth rubs over a 5-second period with abrasive paper ("WET OR DRY - TRIMITE"
  • MeFOSE(M)A N-methyl perfluorooctyl sulfonamidoethyl(meth)acrylate
  • OD(M)A octadecyl(meth)acrylate
  • AIBN azo-isobutyronitrile
  • FC fluorochemical oil- and water- repellent leather protector based on fluoroaliphatic esters of dimer acids and/or trimer acids.
  • Si-Mac polydimethylsiloxane macromer, available in different molecular weight, from Shin-Etsu All parts, ratios, percentages etc. in the following examples and the rest of the specification are by weight unless otherwise noted.
  • Examples 1 to 6 several amphiphilic fluorochemical copolymers as given in Table 1, prepared according to the general procedure were tested on wet blue leather obtained from Rompa Leder (Netherlands). The leather had a thickness between 2.0 - 2.2 mm. The wet blue leather was tanned according to a general procedure to prepare shoe upper leather.
  • the treatment agent of Comparative Example C-l did not contain any fluorochemical monomer and the treatment agent of Comparative Example C-2, did not contain hydrocarbon monomer.
  • the leather was treated according to the general procedure as described above. After the different treatment steps, the leather was horsed-up overnight and dried at 60°C during 60 min. After softening and conditioning for 2 weeks at room temperature, the leather was tested according to the ASTM D-2009-70 test. The results of waterproofness are given in Table 1.
  • Table 1 Composition of Amphiphilic Fluorochemical Copolymers and Waterproofing Properties of Leather Treated Therewith
  • amphiphilic fluorochemical copolymers impart a high degree of waterproofness to leather treated therewith.
  • the use of small amounts (10 % by weight) of fluorochemical (meth)acrylate in the polymer increases the waterproofness dramatically.
  • the amount of long chain alkyl hydrocarbon monomer is preferably more than 20% by weight.
  • Example 7 and Comparative Example C-3 In Example 7 a polymer was prepared from MeFOSEMA/ODMA/AA
  • Example 8 the polymer of Example 8 was made with stearylmercaptan as chain transfer agent instead of mercaptoacetic acid.
  • Example 12 an amphiphilic fluorochemical copolymer was prepared from MeFOSEMA/ODMA/IBMA/AA 20/40/10/30 according to the general procedure and neutralized with triethanolamine.
  • Wet blue leather (1.7 mm) was treated with the amphiphilic fluorochemical copolymer dispersion at 4% by weight based on the shaved weight of the leather.
  • the leather was tested for its waterproofness. The test was stopped after 140.000 Maeser flexes were obtained. This result indicates that also short chain alkyl acrylates can be incorporated in the amphiphilic fluorochemical copolymers without damaging the waterproofing properties of the leather treated therewith.
  • amphiphilic fluorochemical copolymers were made from 23 parts MeFOSEA, 23 parts ODMA, 30 parts AA and 23 parts siloxane macromer.
  • the polymers were made according to the general procedure, but using DPM as solvent.
  • the polymers were dispersed using triethanolamine or sodiumhydroxide.
  • the dispersions were applied to wet blue leather (1.7 mm) at 4% by weight based on the shaved weight of the leather.
  • the results of water repellency (mean values of 3 measurements) are given in Table 3.
  • Table 3 Waterproofness of Wet Blue leather Treated with Amphiphilic
  • Example 18 an amphiphilic fluorochemical copolymer was made from 30 parts MeFOSEMA, 40 parts ODMA and 30 parts AA. The polymer was neutralized with triethanolamine. A blend of 80 parts of the polymer dispersion and 20 parts of a conventional fluorochemical oil-and water repellent leather protector FC was applied to wet blue leather (1.7 mm) at 4% based on the shaved weight of the leather. The treated leather was tested for oil and water repellency. The results are given in Table 4.
  • Example 19 and Comparative Example C-4 The same kind of experiment was repeated in Example 19 and Comparative Example C-4.
  • Example C-4 but with Bovine nubuck leather (for shoe upper leather).
  • Bovine nubuck leather for shoe upper leather.
  • the leather was treated with a mixture of 4% amphiphilic fluorochemical copolymer and 4% of a conventional fluorochemical oil- and water repellent leather protector FC.
  • Comparative Example C-4 was made using 4% LubritanTM WP in combination with 4% FC. The results of water and oil repellency are given in Table 5.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

La présente invention concerne un copolymère amphiphile composé des unités récurrentes: (I) et (II) où: Rf représente un groupe alkyle fluoré contenant au moins 3 atomes de carbone; Q et Q' représentent chacun indépendamment un groupe de liaison organique ou une liaison chimique; R1 et R2 représentent chacun indépendamment de l'hydrogène ou un groupe alkyle C¿1? à C4; et Rh représente un groupe hydrocarbure ayant au moins 8 atomes de carbone et, éventuellement, de 1 à 3 substituants; ainsi qu'une unité récurrente comprenant au moins un groupe acide carboxylique ou un sel de celui-ci. La présente invention concerne également un procédé de fabrication du copolymère amphiphile ci-dessus, qui peut être utilisé dans le traitement du cuir pour le rendre imperméable.
PCT/US1997/018386 1996-11-07 1997-10-15 Utilisation de copolymeres amphiphiles contenant un monomere fluore pour rendre un cuir impermeable WO1998020170A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US09/297,814 US6294103B1 (en) 1996-11-07 1997-10-15 Use of amphiphilic copolymers containing a fluorinated monomer to impart waterproofness to leather
BR9712754-0A BR9712754A (pt) 1996-11-07 1997-10-15 Processo de tratamento de couro, copolìmero anfifìlico, uso e processo de obtenção do mesmo, couro, e, composição aquosa.
JP52140298A JP3911549B2 (ja) 1996-11-07 1997-10-15 皮革に防水性を与えるためのフッ素化モノマー含有両親媒性コポリマーの使用法
AU48998/97A AU4899897A (en) 1996-11-07 1997-10-15 Use of amphiphilic copolymers containing a fluorinated monomer to impart waterproofness to leather

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP96117814.2 1996-11-07
EP96117814A EP0841405B1 (fr) 1996-11-07 1996-11-07 Utilisation de copolymères amphiphiles contenant des monomères fluorés pour imperméabiliser des cuirs

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WO1998020170A1 true WO1998020170A1 (fr) 1998-05-14

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KR (1) KR100475495B1 (fr)
CN (1) CN1152142C (fr)
AR (1) AR009410A1 (fr)
AU (1) AU4899897A (fr)
BR (1) BR9712754A (fr)
DE (1) DE69605925T2 (fr)
ES (1) ES2143125T3 (fr)
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6525127B1 (en) 1999-05-11 2003-02-25 3M Innovative Properties Company Alkylated fluorochemical oligomers and use thereof in the treatment of fibrous substrates
KR101121910B1 (ko) * 2006-06-13 2012-03-20 와커 헤미 아게 β-케토카르보닐 작용성 실록산 중합체를 사용하여 단백질을 함유하는 섬유질 물질을 처리하는 방법

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA04007382A (es) * 2002-01-31 2004-10-11 Tfl Ledertechnik Gmbh Composiciones y su uso para impartir repelencia al agua a cuero o pieles, textiles y otros materiales fibrosos.
KR20030073514A (ko) * 2002-03-12 2003-09-19 강석일 방수막을 가지는 먹장어 가죽 및 그 제조방법
EP1820809A1 (fr) 2006-02-17 2007-08-22 Lanxess Deutschland GmbH Revêtement de substrats à base de polymères fluorés réticulables
EP1801133A1 (fr) 2005-12-19 2007-06-27 Lanxess Deutschland GmbH Copolymères durcissables fluorés et revêtements ainsi que leur procèdé de préparation

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0324354A2 (fr) * 1988-01-14 1989-07-19 Bayer Ag Polymères greffés, leur procédé de préparation et leur utilisation
EP0426530A1 (fr) * 1989-11-02 1991-05-08 Elf Atochem S.A. Télomerès acryliques fluorés et leur application au traitement hydrofuge et oléofuge de substrats divers
DE4240274A1 (de) * 1992-12-01 1994-06-09 Minnesota Mining & Mfg Polysiloxane mit fluoraliphaten- und carboxylhaltigen terminalen Gruppen, ihre Herstellung und ihre Verwendung bei der Behandlung von Fasersubstraten

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2803615A (en) 1956-01-23 1957-08-20 Minnesota Mining & Mfg Fluorocarbon acrylate and methacrylate esters and polymers
US3923715A (en) 1973-07-26 1975-12-02 Du Pont Aqueous dispersions of perfluoroalkyl esters and vinyl polymers for treating textiles
US4525305A (en) 1982-10-25 1985-06-25 Minnesota Mining And Manufacturing Company Leather with fluorochemical finish
US4539006A (en) 1983-09-13 1985-09-03 Minnesota Mining And Manufacturing Company Leather treatment
DE3672718D1 (de) 1985-08-30 1990-08-23 Hoechst Ag Perfluoralkyl- und epichlorhydrin-gruppen enthaltende urethane, diese urethane enthaltende waessrige dispersionen und ihre verwendung.
FR2588555B1 (fr) 1985-10-16 1987-12-11 Atochem Monomeres acryliques fluores, polymeres en derivant et leur application au traitement hydrofuge et oleofuge de substrats divers
FR2590895B1 (fr) 1985-12-03 1988-01-15 Atochem Monomeres acryliques fluores, polymeres en derivant et leur application comme agents hydrophobes et oleophobes
DE3622284A1 (de) 1986-07-03 1988-01-07 Hoechst Ag Urethane aus aliphatischen fluoralkoholen, isocyanaten und aromatischen verbindungen, verfahren zu ihrer herstellung und ihre verwendung
DE3722375A1 (de) 1987-07-07 1989-01-19 Hoechst Ag Fluor und polysiloxan enthaltende urethane, verfahren zu ihrer herstellung und ihre verwendung
DE3800629A1 (de) 1988-01-12 1989-07-20 Basf Ag Verfahren zum hydrophobieren von leder, pelzen und lederaustauschmaterialien
TNSN89128A1 (fr) 1988-12-02 1991-02-04 Rohn And Haas Company Independance Mall West Traitement du cuir avec des copolymeres amphiphites choisis
DE3931039A1 (de) 1989-09-16 1991-03-28 Basf Ag Verwendung von copolymerisaten auf basis von langkettigen ungesaettigten estern und ethylenisch ungesaettigten carbonsaeuren zum hydrophobieren von leder und pelzfellen
CA2071596A1 (fr) 1991-07-10 1993-01-11 Frederick E. Behr Halogenures de perfluoroalkyle et leurs derives
EP0613462B1 (fr) 1991-11-12 1996-01-17 Minnesota Mining And Manufacturing Company Derives de l'acide dimere fluoroaliphatique et leur utilisation
DE4223111A1 (de) 1992-07-14 1994-01-20 Henkel Kgaa Neue Lederfettungsmittel und ihre Verwendung
DE4244951C2 (de) 1992-12-01 1998-08-06 Minnesota Mining & Mfg Fasersubstrat mit Wasser-, Öl-, Schmutzabweisungsvermögen und Weichgriffigkeit
DE4416415A1 (de) 1994-05-10 1995-11-16 Hoechst Ag Copolymere auf Basis von ethylenisch ungesättigten Dicarbonsäureanhydriden, langkettigen Olefinen und Fluorolefinen

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0324354A2 (fr) * 1988-01-14 1989-07-19 Bayer Ag Polymères greffés, leur procédé de préparation et leur utilisation
EP0426530A1 (fr) * 1989-11-02 1991-05-08 Elf Atochem S.A. Télomerès acryliques fluorés et leur application au traitement hydrofuge et oléofuge de substrats divers
DE4240274A1 (de) * 1992-12-01 1994-06-09 Minnesota Mining & Mfg Polysiloxane mit fluoraliphaten- und carboxylhaltigen terminalen Gruppen, ihre Herstellung und ihre Verwendung bei der Behandlung von Fasersubstraten

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6525127B1 (en) 1999-05-11 2003-02-25 3M Innovative Properties Company Alkylated fluorochemical oligomers and use thereof in the treatment of fibrous substrates
KR101121910B1 (ko) * 2006-06-13 2012-03-20 와커 헤미 아게 β-케토카르보닐 작용성 실록산 중합체를 사용하여 단백질을 함유하는 섬유질 물질을 처리하는 방법

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TW419524B (en) 2001-01-21
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BR9712754A (pt) 1999-10-19
DE69605925T2 (de) 2000-07-20
CN1152142C (zh) 2004-06-02
ES2143125T3 (es) 2000-05-01
EP0841405B1 (fr) 1999-12-29
CN1236397A (zh) 1999-11-24
KR20000053098A (ko) 2000-08-25
KR100475495B1 (ko) 2005-03-10
AR009410A1 (es) 2000-04-12
AU4899897A (en) 1998-05-29
JP2001504874A (ja) 2001-04-10
EP0841405A1 (fr) 1998-05-13

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