FI83531B - FLUORERADE COPYER OVER ANVAENDNING AV DEM FOER BEHANDLING AV OLIKA SUBSTRAT FOER ATT GOERA DEM VATTEN- OCH OLJEAVSTOETANDE. - Google Patents

Abstract

1. Claims for the contracting States BE, CH, DE, FR, GB, IT, LI, LU, NL, SE Fluoro copolymers, characterized in that they comprise, by weight : (a) 30 to 70% of one or more polyfluoro monomers of general formula : see diagramm : EP0195714,P13,F3 in which R**f denotes a straight- or branched-chain perfluoro radical containing 2 to 20 carbon atoms, Q denotes an oxygen or sulphur atom, B denotes a divalent chain sequence linked to Q via a carbon and capable of containing one or more oxygen, sulphur and/or nitrogen atoms, one of the symbols R denotes a hydrogen atom and the other a hydrogen atom or an alkyl radical containing 1 to 4 carbon atoms ; (b) 10 to 50% of one or more monomers of general formula : see diagramm : EP0195714,P13,F4 in which R**1 denotes a hydrogen atom or a methyl radical, R**2 denotes an alkyl radical containing 1 to 4 carbon atoms, n is equal to 2 or 3 ; and optionally (c) up to 40% of any one or more monomers other than those of formulae (I) and (II). 1. Claims for the Contracting state AT Process for the preparation of fluorinated products, characterized in that there are copolymerized, by weight : (a) 30 to 70% of one or more polyfluoro monomers of general formula : see diagramm : EP0195714,P14,F2 in which Rf denotes a straight- or branched-chain perfluoro radical containing 2 to 20 carbon atoms, Q denotes an oxygen or sulphur atom, B denotes a divalent chain sequence linked to Q via a carbon and capable of containing one or more oxygen, sulphur and/or nitrogen atoms, one of the symbols R denotes a hydrogen atom and the other a hydrogen atom or an alkyl radical containing 1 to 4 carbon atoms ; (b) 10 to 50% of one or more monomers of general formula : see diagramm : EP0195714,P14,F3 in which R1 denotes a hydrogen atom or a methyl radical, R2 denotes an alkyl radical containing 1 to 4 carbon atoms, n is equal to 2 or 3 ; and optionally (c) up to 40% of any one of more monomers other than those of formulae (I) and (II) ; within an organic solvent and in the presence of a polymerization catalyst and/or of a photoinitiator.

Description

1 83531

The present invention relates to novel fluorinated copolymers and their use in the treatment of various substrates, such as paper, textiles, wood, nonwovens, metals, concrete plastics and especially leather, as water and oil repellents.

Chromium complex compounds of fluorinated carboxylic acids have been proposed as particularly suitable products for leather (U.S. Patents 2,934,450, 3,651,105, 3,907,576 and 3,574,518). Although these complex compounds effectively provide good properties, their disadvantage is that they are strongly greenish and impart this color to the substrates to which they are applied, which limits their use.

Fluorinated acrylate polymers and copolymers (U.S. Patent 3,524,760) and fluorocarbonated ____ carbamates and dicarbamates (U.S. Patent 3,657,320) have also been proposed. However, the use of these products, which require the use of an organic, very often halogenated, solvent, requires certain precautions to be taken in order not to contaminate the environment.

Also known are fluorocarboxylic acids (U.S. Patent 3,382,097) and polyfluoroalkylthiodicarboxylic acids (U.S. Patent 3,471,518). The water and oil repellent properties of these products on the skins are low.

New fluorinated products have now been invented in the applicant's industrial plants which, when applied to hides and skins, give them excellent water and oil repellent properties without affecting their color, appearance or feel. In addition, these products are very easy to use and do not pose any danger to the environment.

The products according to the invention are copolymers characterized in that they comprise, by weight: (a) 50-65% of one or more polyfluoromonomers of the general formula:

II

Rf-BQCC = CH2 (I) ch3 wherein Rf is a straight or branched perfluorinated radical containing from 2 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, Q is an oxygen or sulfur atom, B is a divalent chain bonded to Q : and may contain one or more oxygen, sulfur and / or nitrogen atoms; (b) 32.5 to 50% of one or more monomers of the general formula:

II

H2C = C-C-O [CnH2nO] -R2 (II) I3 R1 wherein R1 is a hydrogen atom or a methyl radical, R2 is an alkyl radical having 1 to 4 carbon atoms, n is 2 or 3; and optionally (c) up to 10% of one or more monomers selected from vinyl acetate, acrylic or methacrylic acid, maleic anhydride, alkyl acrylates or methacrylates, ethylene glycol or triethylene glycol diacrylates, dimethacrylates, dimethacrylates or dimethacrylates ethylene glycol or propylene glycol monoacrylates or methacrylates, acrylamide, methacrylamide, N-methylol-3 83531 acrylamide or methacrylamide, N, N-dimethylaminoethyl or N-tert-butylaminoacetylmethyl

As the polyfluoro monomers of the formula (I), those corresponding to the formula are preferably used:

II

Rf- (CH2) p-O-C-C = CH2 (III) ch3 wherein Rf is as defined above, p is an integer from 1 to 20, preferably 2 or 4. These monomers can be prepared by known methods, e.g. by esterification of the corresponding compounds of formula:

Rf- (CH2) p-OH (IV) alcohols with an alkene monocarboxylic acid having the formula: H00C-C = CH? (V) ch3 such as e.g. acrylic acid, methacrylic acid, crotonic acid, in the presence of acid catalysts such as sulfuric acid or p-toluenesulfonic acid. Instead of alkene monocarboxylic acids of the formula (V), their esters, anhydrides or halides can also be used. For reasons of profitability and practicality, it has proved particularly advantageous to use a mixture of monomers of the formula (III) in which the Rf radicals are different.

Other examples of polyfluoromonomers of formula (I) include esters of acids of formula (V) with alcohols and thiols of the formulas:

Y

Rf- (CH2) p-SO2-N- (CXX ') q-C-OH (VI) R3 Y'

Rf- (CH2) p-SH (VII)

Rf- (CH2) p-O- (CH2) r-OH (VIII) 4 83531

Rf - (CH2) p - s - (CH2) r - OH (IX)

Rf - (CH2) p - (OCH2CH2) r - OH (X)

Rf - (CH2) p - SO2 - (CH2) r - OH (XI)

Rf - CH = CH - (CH2) p - OH (XII)

Rf - SO 2 - N - (CH 2) p --OH (XIII)

Rf - COO - (CH 2) p --0H (XIV)

Rf - CO - N - (CH2) p - OH (xv) R4 wherein Rf and p are as defined above, r3 is a hydrogen atom or an alkyl radical having 1 to 10 carbon atoms (preferably methyl), R4 is a hydrogen atom or an alkyl radical, having 1 to 4 carbon atoms, q is an integer from 1 to 4 (preferably 1 or 2), r is an integer from 1 to 20: (preferably 1 to 4), X, X ', Y and Y' are the same or various ·· and each represent a hydrogen atom or an alkyl radical having 1 to 4 carbon atoms.

Examples of monomers of the formula (III) which may be mentioned are, in particular, the methyl or ethyl ether acrylates and methacrylates of triethylene glycol or tripropylene glycol. In general, the monomers of the formula (II) are obtained in a manner known per se by esterification of the corresponding ether alcohols of the formula: HO - [cnH2no] 3 - R2 with an acrylic or methacrylic acid or a derivative of this acid.

5,83531

The products according to the invention are prepared in a manner known per se by copolymerizing monomers dissolved in an organic solvent or organic solvents such as acetone, methyl ethyl ketone, Y-butyrolactone, methylcyclohexanone, N-methyl-2-pyrrolidone, ethanol, butanol, ethanol, isopropyl alcohol, isopropyl alcohol diacetone alcohol, phenylmethylcarbinol, isophorone, tetrahydrofuran, dioxane, ethyl acetate, glycol acetate, ethylene or polyethylene glycol monomethyl or monoalkyl ether, dimethylamidone, acetylene or polypropylene glycol, ethylene, or polypropylene glycol monomethyl, or to the mixture. It has been found advantageous to use water-miscible solvents such as acetone, ethyl or isopropyl alcohol, monoalkyl ethers of polyethylene or polypropylene glycol.

Suitable polymerization catalysts are used, such as, for example, benzoyl peroxide, lauroyl peroxide, acetyl peroxide, succinyl peroxide, 2,2'-azobis-isobutyronitrile, 2,2'-azobis (2,4-dimethyl-4-methoxysivaleronitrile), 4,4 ' -azobis (4-cyanovaleric acid), in the presence of azodicarbonamide, tert-butyl perpivalate. The amount of catalyst used may vary from 0.01 to 5%, preferably from 0.1 to 2%, of the total weight of the monomers used.

6 83531

It is also possible to operate using a source of UV radiation in the presence of photoinitiators such as benzophenone, 2-methylanthraquinone or 2-chlorothioxanthone.

The reaction temperature can vary within wide limits, i.e. between room temperature and the boiling temperature of the reaction mixture. Preferably operated at 50-90 ° C.

If it is desired to control the molecular weight of the copolymers, alkyl mercaptan-like chain transfer agents such as tert-dodecyl mercaptan, n-dodecyl mercaptan, n-octyl mercaptan, carbon tetrachloride, triphenyl methane can be used. The amounts used, depending on the values desired for the molecular weights, may vary from 0.01 to 3%, and preferably from 0.05 to 0.5%, of the total weight of the monomers.

The resulting copolymer mixture may optionally be diluted with a copolymerization solvent or, provided they are miscible, as another solvent, water or a mixture of a solvent and water. If desired, the copolymer can also be separated by eliminating the solvent or solvents.

As substrates which can be treated to repel oil or water with the products according to the invention, mention may be made in particular of hides. Other various materials may be mentioned, such as papers, woven fabrics based on cellulose or regenerated cellulose, natural, synthetic or synthetic fibers such as cotton, cellulose acetate, wool, silk, polyamide, polyester, polyolefin, polyurethane or polyacrylonitrile fibers. articles or nonwovens, plastics, glass, wood, metals, porcelain, bricks and other masonry materials, painted surfaces. The products according to the invention can be added to cosmetic compositions, for example hair sprays.

In the case of hides and skins, the copolymer solutions according to the invention are applied mainly in an alcoholic, hydroalcoholic or aqueous medium, using well-known methods, for example by spraying, immersion in a bath in a cotton swab or paddle bath or brush application.

Substrates treated with the copolymers of the invention are highly oil and water repellent after drying at a simple room temperature or higher, which varies depending on the type of substrate and may rise to 250 ° C. The skins are preferably dried at room temperature or at a reasonable temperature rising to about 60 ° C.

In order to achieve a special effect or better adhesion of Jorik, it may sometimes be advantageous in some substrates to incorporate the copolymers according to the invention into certain additives, polymers, thermosetting agents and catalysts.

The amount of copolymer used varies depending on the quality of the substrate to be treated::: and the fluorine content of the copolymer. In the case of leather, this amount is generally 0.2-5 g / m 2, preferably 0.5-2.5 g / m 2. When treated in this way, all types of hides tanned with chromium salts or herbal tanning agents are highly oil and water repellent.

To assess the performance of the substrates treated according to the invention, the applicant has used the following tests:

Water resistance test (RE) This test measures the time taken for a drop of water placed on a substrate to penetrate the substrate. If this time is more than two hours, the water resistance is rated as excellent.

8 83531 01 Endurance test (RH)

The test measures the time taken for a drop of copper linseed oil placed on a substrate to penetrate the substrate. If the time is more than two hours, the oil resistance is rated as excellent.

Water repellency test (H)

In certain media, water repellency was measured with test solutions numbered 1 to 10, consisting of mixtures of water and isopropanol containing these substances in the following weight ratios:

Test solution Water Isopropanol 1 90 10 2 80 20 3 70 30 4 60 40 5 50 50 6 40 60 7 30 70: 8 20 80 9 10 90 10 0 100

In the test, drops of these mixtures are placed on the treated substrates and then their effect is examined. Scores are given as numbers corresponding to the solution containing the highest percentage of isopropanol that has not gone to the substrate or irrigated after a contact time of 30 seconds.

The repellency of the treated to oils (OR) and water (§T) was measured according to AATCC 118-1975 (Oil Repellency: hydrocarbon resistance test) and AATCC 22-1975 (Water repellency: Spray test). From the leather, the water test (spray test) was determined as follows: when all the water has been poured on the surface of the leather, it is placed on its patch and covered with 9 83531 sheets of absorbent paper; then the assembly is subjected to compression by moving a 2 kg metal roll back and forth over it. The score is then given on the basis of the stains formed by the skin's moisturizing water and according to the values mentioned in the evaluation table of standard AATCC 22-1975.

To evaluate the performance of papers treated according to the invention, the applicant also used the following tests: Turpentine test This test is described in Tappi, standard T 454, i.e. 66 (1966). On the paper to be tested, which is itself placed on white bristol board, 5 g of acid-washed Kontainebleau sand is applied, then 1.1 ml of anhydrous turpentine stained with 0.5 g / l of Organol BS red are poured onto the sand. Once the turpentine is poured, start the chronometer and transfer the paper every 30 seconds with the cardboard. Note the time that has elapsed when a stain appears on the cardboard. After 30 minutes, the test can be considered insignificant and the performance of the tested substrate is judged to be excellent. The experiment was performed on 7 specimens of the same paper. Record the values from lowest to highest --- and note that the fourth value is the average value.

Grease resistance test or "Kit value" With this test, which is described in the Tappi publication, you can. 5, No. 10, pages 152 A and 153 A, standard RC 338 and UM 511, "· the grease resistance of substrates can be measured with mixtures of castor oil, toluene and heptane used in different quantities.

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Kit Chapter Volume of castor oil Toluene Heptane Volume Volume 1 200 0 0 2 180 10 10 3 160 20 20 4 140 30 30 5 120 40 40 6 100 50 50 7 80 60 60 8 60 70 70 9 40 30 80 10 20 90 90 11 0 100 100 12 0 90 110

Carefully place drops of these mixtures on the paper treated in the test. Allow the droplets to remain on the paper for 15 seconds, then carefully inspect the appearance of the papers or cardboard and record any wetting or absorption that appears as a browning of the surface. The figure corresponding to the mixture containing the highest percentage of heptane that does not penetrate or wet the paper is the "kit value" of the paper and is considered to be the degree of oil rejection of the treated paper. The higher the "kit value", the better the paper repels oil.

The following examples, in which parts and percentages are by weight unless otherwise indicated, illustrate the invention without limiting it.

Example 1

A reactor having a capacity of 250 parts by volume and equipped with a reflux condenser, a thermometer, a nitrogen inlet and a heating device is charged with 60 parts of isopropyl alcohol, 25 parts of triethylene glycol methyl ether methacrylate and 25 parts of a mixture of polyfluoromonomers containing 8,83531 Ci'2) u - C2H4 - O - C - C = CH2 ch3 where n is 5, 7, 9, 11, 13 and 15 in average weight ratios and 1: 56: 22: 9: 3: 3, respectively. The air is removed from the reactor by a stream of nitrogen for 15 minutes and the temperature is raised to 80 ° C. Then, 0.5 part of 4,4'-bis (4-cyanovaleric acid) is added and the temperature is maintained at 80 ° C for 4 hours, adding 0.1 part of t-butyl perpivalate after one hour. The mixture is then diluted with 25 parts of water and 25 parts of isopropanol before cooling to room temperature. In this way, a solution (SI) of the copolymer according to the invention is obtained. This solution contains 30.5% non-volatile matter and has a fluorine content of 9.4%.

Dilute 2 grams of this solution to 100% with a mixture of Ia containing 50/50 water and isopropanol. This new solution (Sld) is applied by spraying on chromium tanned ·: - · fully embroidered calfskin at 200 g / m 2 and allowed to dry: for four hours at room temperature before examining the performance obtained. The results obtained are shown in the following table compared to untreated leather: 12 83531

Chrome-tanned fully embroidered calfskin Features Treated Untreated

Water resistance (RE) over 2 hours 25 seconds 01stool resistance (RH) over 2 hours 105 seconds

Oil repellency (OR) AATCC 110-1975 3 0

Water repellency (ST)

Spray test AATCC 22-1975 100 0

Example 2

In an apparatus similar to Example 1, 60 parts of L sopropoly alcohol, 16.25 parts of triethylene glycol methyl ether, acrylate, 1.25 parts of acrylic acid and 32.5 parts of the same mixture of polyfluoromonomers as in Example 1 are introduced. The air is removed from the reactor by a stream of nitrogen. for one minute and the temperature is raised to 80 ° C. 0.5 part of 4,4'-bis (4-cyanovaleric acid) is then added and the temperature is maintained at 80 ° C for 4 hours, adding 0.1 part of t-butyl perpivalate every hour. The mixture is then diluted with a solution of 25 parts of water, 25 parts of isopropyl alcohol and 0.8 parts of potassium hydroxide before cooling to room temperature. This gives a solution (S2) of the copolymer according to the invention. This solution, which contains 30.6 parts of non-volatile substances and has a fluorine content of 12.1%, is applied to unleaved paper having the following characteristics: - Fiber composition; 60% hardwood-based bleached kraft pulp 40% softwood-based bleached kraft pulp 13,83531

- Grinding with a hydrafiner 00 to 35 ° SR

- Additives used; talc: 15% filler (Bayer's RETAMINOL E): 3% - Paper weight: 70-71 g / m 2 - Paper moisture content: 4-5%.

For this purpose, a bath containing 0.85 g of fluorine / liter is prepared for the size press by diluting 7 g of solution S2 with 993 g of water. The sheet of non-adhesive paper is treated with a sizing press in this bath at a flow rate of 05 S. After drying for 90 seconds at 110 ° C, a paper which is highly water and oil repellent is obtained, as shown by the results in the following table compared to untreated paper.

____: Properties Treated Paper Untreated Paper 01Skin Value (Kit value) .7 0 Turpentine test over 30 minutes less than 30 seconds 01Synthesis (RH) over 2 hours less than 60 seconds

Example 3 - · Proceed as in Example 1, but replace the mixture of polyfluoromonomers with the same amount (25 parts) of monomer of formula: o / 1 C6Fi3 - C2H4 - o - c - c = ch2 ch3 14 83531 The solution thus obtained (S3) contains 30.8 non-volatile substances and has a fluorine content of 8.8%.

Example 4

Proceed as in Example 1, but using 16.25 parts of triethylene glycol methyl ether methacrylate, 1.25 parts of 2-sulfoethyl methacrylate and 32.5 parts of the same mixture of polyfluoromonomers as in Example 1.

The solution (S4) thus obtained contains 30.9% of non-volatile substances and has a fluorine content of 12.4%.

Example 5

Proceed as in Example 2, but using 23.75 parts of tripropylene glycol methyl ether methacrylate, 1.2 parts of acrylic acid and 25 parts of the same mixture of polyfluoromonomers as in Example 1.

The solution (S5) thus obtained contains 30.8% of non-volatile substances and has a fluorine content of 9.5%.

.: Example 6

Proceed as in Example 1, but use as monomers! 25 parts of triethylene glycol methyl ether methacrylate, and 25 parts of the same mixture of polyfluoromonomers as in Example 1.

The solution (S6) thus obtained contains 30.9% of non-volatile substances and has a fluorine content of 9.5%.

Example 7

Proceed as in Example 1, but using 20 parts of triethylene glycol methyl ether methacrylate, 5 parts of 2-isocyanate ethyl ethyl methacrylate and 25 parts of the same mixture of polyfluoromonomers as in Example 1.

The solution (S7) thus obtained contains 30.8% of non-volatile matter and has a fluorine content of 9.5%.

Example 8 (comparative example)

Proceed as in Example 1, but instead of the polyfluoromonomer mixture, the same amount (25 parts) of a mixture of polyfluoro monomers having the formula: and 15 in average weight ratios and 1:50: 31: 10: 3: 1: 1, respectively.

The solution thus obtained (S8) contains 31.3% of non-volatile substances and has a fluorine content of 7.2%.

Example 9

Proceed as in Example 1, but using 20 parts of triethylene glycol methyl ether methacrylate, 5 parts of vinyl acetate and 25 parts of the same mixture of polyfluoromonomers as in Example 1.

The solution (S9) thus obtained contains 30.5% of non-volatile substances and has a fluorine content of 9.4%.

Example 10

Proceed as in Example 1, but using less (22.5 parts) triethylene glycol methyl ether methacrylate and more (27.5 parts) polyfluoromonomers.

The solution thus obtained (S10) contains 30.8% of non-volatile substances and has a fluorine content of 10.5%.

Example 11

Proceed as in Example 2, but using 20 parts of triethylene glycol methyl ether methacrylate, 5 16 83531 parts of N-tert-butylaminoethyl methacrylate and 25 parts of the same mixture of polyfluoromonomers as in Example 1.

The solution thus obtained (SI1) contains 30.7% of non-volatile substances and has a fluorine content of 9.3%.

JSample 12

Proceed as in Example 2, but replace acrylic acid with the same amount (1.25 parts) of N, N-dimethylaminoethyl methacrylate and potassium hydroxide with 1 part of acetic acid.

The solution thus obtained (S12) contains 30.6% of non-volatile substances and has a fluorine content of 12.3%.

Example 13

Solutions 33, S4, S5, S6, S7, S8, S9 and S10 are diluted with 50/50 water and isopropanol to give solutions S3d, S4d, S5d, S6d, S7d, S8d, S9d and S10d each containing 0, 19% fluorine, then these diluted solutions are applied to the same skin and under the same conditions as in Example 1.

The following table, in which the symbol "++" means "more than two hours", summarizes the results obtained in comparison with untreated leather.

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Treatment solution RE RH ST

Without (untreated leather) 25 seconds 105 seconds 0 S3d ++ ++ 100 S4d ++ ++ 100 S5d ++ ++ 90 S6d ++ ++ 90 S7d ++ ++ 100 S8d 90 minutes ++ 100 S9d ++ + + 100

SlOd ++ ++ 100

Example 14

By diluting 5.7 g of the solution S12 of Example 12 with 994.3 g of water, a bath containing 0.7 g of fluorine / liter is prepared for the size press and treated with a non-adhesive sheet of paper having the same properties and treated under the same conditions as in Example 2. following results: Treated paper Untreated paper Oil value repellency (Kit value) 8 0 Turpentine test more than 30 minutes less than 30 seconds

Water resistance (RE) more than 2 hours less than 15 seconds Oil resistance (RH) more than 2 hours less than 1 minute Oil repellency (H) 9 0

Claims (6)

Copolymers, characterized in that they comprise by weight as a percentage: i.e. 83531 (a) 50-65% of one or more polyfluoromonomers of the general formula: 0 I! Rf-BQCC = CH2 (I) ch3 wherein Rf is a straight or branched perfluorinated radical containing from 2 to 20 carbon atoms, preferably from 4 to 16 carbon atoms, Q is an oxygen or sulfur atom, B is a divalent chain bonded to Q : and may contain one or more oxygen, sulfur and / or nitrogen atoms; (b) 32.5-50% of one or more monomers of the general formula: O II H2C = CC-O [CnH2nO] -R2 (II) I3R1 wherein R1 is a hydrogen atom or a methyl radical, R2 is an alkyl radical, having 1 to 4 carbon atoms, n is 2 or 3; and optionally (c) up to 10% of one or more monomers selected from vinyl acetate, acrylic or methacrylic acid, maleic anhydride, alkyl acrylates or methacrylates, ethylene glycol or triethylene glycol diacrylates, diacrylate or diacetate ethylene glycol or propylene glycol monoacrylates or methacrylates, acrylamide, methacrylamide, N-methylol-9 83531 acrylamide or methacrylamide, N, N-dimethylaminoethyl or N-tert-butylacetylaminoethyl Copolymers according to Claim 1, characterized in that the polyfluoromonomer or polyfluoromonomers have the formula: O II Rf- (CH 2) p -O-CC = CH 2 (III) ch 3 in which R f is as defined in Claim 1 and p is an integer from 1 to 20 , preferably 2 or 4. Copolymers according to Claim 2, characterized in that they are prepared using monomers of the formula (III) in which the Rf radicals are different. Copolymers according to one of Claims 1 to 3, characterized in that R 2 is a methyl or ethyl radical. Use of copolymers according to one of Claims 1 to 4 for the treatment of various substrates, in particular hides, as oil and water repellents. Substances and preparations treated with a copolymer according to any one of claims 1 to 4.