EP0121078B1 - Produits auxiliaires textiles - Google Patents
Produits auxiliaires textiles Download PDFInfo
- Publication number
- EP0121078B1 EP0121078B1 EP19840101888 EP84101888A EP0121078B1 EP 0121078 B1 EP0121078 B1 EP 0121078B1 EP 19840101888 EP19840101888 EP 19840101888 EP 84101888 A EP84101888 A EP 84101888A EP 0121078 B1 EP0121078 B1 EP 0121078B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- textile
- atoms
- und
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000004753 textile Substances 0.000 title claims description 14
- 239000006185 dispersion Substances 0.000 claims description 22
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 18
- -1 amino, mercapto Chemical group 0.000 claims description 17
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 13
- 239000000725 suspension Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 238000009988 textile finishing Methods 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 6
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 239000011737 fluorine Substances 0.000 claims description 5
- 229920000620 organic polymer Polymers 0.000 claims description 5
- 239000002952 polymeric resin Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 125000003700 epoxy group Chemical group 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical group 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims 1
- 125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 238000012360 testing method Methods 0.000 description 17
- 229920001577 copolymer Polymers 0.000 description 15
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 12
- 239000004744 fabric Substances 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
- 239000003446 ligand Substances 0.000 description 5
- 229910000077 silane Inorganic materials 0.000 description 5
- 150000004756 silanes Chemical class 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000005871 repellent Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 241001295925 Gegenes Species 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 238000004043 dyeing Methods 0.000 description 3
- 239000002657 fibrous material Substances 0.000 description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 239000012928 buffer substance Substances 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- SBRXLTRZCJVAPH-UHFFFAOYSA-N ethyl(trimethoxy)silane Chemical compound CC[Si](OC)(OC)OC SBRXLTRZCJVAPH-UHFFFAOYSA-N 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 2
- HLXDKGBELJJMHR-UHFFFAOYSA-N methyl-tri(propan-2-yloxy)silane Chemical compound CC(C)O[Si](C)(OC(C)C)OC(C)C HLXDKGBELJJMHR-UHFFFAOYSA-N 0.000 description 2
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- ALVYUZIFSCKIFP-UHFFFAOYSA-N triethoxy(2-methylpropyl)silane Chemical compound CCO[Si](CC(C)C)(OCC)OCC ALVYUZIFSCKIFP-UHFFFAOYSA-N 0.000 description 2
- DENFJSAFJTVPJR-UHFFFAOYSA-N triethoxy(ethyl)silane Chemical compound CCO[Si](CC)(OCC)OCC DENFJSAFJTVPJR-UHFFFAOYSA-N 0.000 description 2
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 2
- XYJRNCYWTVGEEG-UHFFFAOYSA-N trimethoxy(2-methylpropyl)silane Chemical compound CO[Si](OC)(OC)CC(C)C XYJRNCYWTVGEEG-UHFFFAOYSA-N 0.000 description 2
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 2
- 238000009732 tufting Methods 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Cc1ccccc1 Chemical compound Cc1ccccc1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- JQALNNOQTGZTJZ-UHFFFAOYSA-N [[4,6-bis[bis(methoxymethyl)amino]-1,3,5-triazin-2-yl]-(methoxymethyl)amino]methanol Chemical compound COCN(CO)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 JQALNNOQTGZTJZ-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000004378 air conditioning Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- GNQQPTRATSISPA-UHFFFAOYSA-N triethoxy(2-ethylbutyl)silane Chemical compound CCO[Si](OCC)(OCC)CC(CC)CC GNQQPTRATSISPA-UHFFFAOYSA-N 0.000 description 1
- RFXMNCFJFSYLMT-UHFFFAOYSA-N triethyl 2-ethylbutyl silicate Chemical compound CCO[Si](OCC)(OCC)OCC(CC)CC RFXMNCFJFSYLMT-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
Classifications
-
- 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
-
- 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/564—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
- D06M15/576—Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them containing fluorine
-
- 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
Definitions
- the present invention relates to a textile finishing agent which allows textile fibers to be made dirt, oil and water repellent.
- Dirt substances can be e.g. of the following composition and consistency: oil and oil-containing substances, liquid, aqueous colored substances, inorganic dry pigment-like substances (street dust), aqueous suspensions of the same and mixtures of the substances mentioned.
- the principle of protective equipment is that the finishing agent gives the pole materials hydrophobic and oleophobic properties that prevent the sinking of liquid contaminants. Dry dirt does not adhere to the fibers and can e.g. can be easily removed by vacuuming from and out of the pile.
- silsesquioxane suspensions described there are, however, relatively unstable and are not universally suitable for dirt-repellent and pole-stabilizing finishing.
- DE-B-1 285 978 discloses a process for rendering oil and water repellant and for reducing the absorption of dry dirt from textile materials.
- substances containing perfluoroalkyl groups are applied to the materials to be protected.
- Organosilsesquioxanes as described, for example, in DE-B-1 594 985 or in DE-A-3 004 824 can be used as component A). These are prepared by, for example, silanes of the general formula R-Si (OR ') 3 alone or together with silanes (Si (OR') 4 in which R is substituted or unsubstituted hydrocarbon radical having 1 to 7 carbon atoms, the substituents of which are halogen atoms, amino, Mercapto and epoxy groups and up to 95% of the radicals R are methyl and R 'is an alkyl radical having 1 to 4 carbon atoms to a mixture of water, a buffer substance, a surface-active agent and optionally an organic solvent with agitation and under acid or basic conditions are added.
- silane In order to achieve a very narrow particle size distribution and a small average pond size of approximately 200 to 500 angstroms, such as are required to achieve optimal pole-stabilizing and dirt-repellent effects, a uniform and slow addition of the amount of silane is required.
- the exact amount of silane that can be added depends on the substituent R and whether an anionic or cationic surfactant is used.
- the simultaneous hydrolysis of the silanes results in copolymers of the silsesquioxanes in which the units can be present in block form or in a random distribution.
- the preferred amount of added silane of the general formula Si (OR ') 4 is 2 to 50%, based on the total amount of the silanes used, preferably 3 to 20% (% by weight).
- the surface-active agents mentioned have the function of stabilizing the particles formed in the colloidal suspension.
- Suitable anionic surfactants are aliphatic and / or aromatic sulfonic acids, for example decyl, dodecyl, cetyl, stearyl, myristic or oleyl sulfonic acids or their alkali metal salts. If cationic surfactants are used, it is advantageous to use halides and especially chlorides and bromides. Other surfactants, including those of a nonionic and amphoteric nature, can be used in conjunction with the above agents provided they do not interfere with the stability of the colloidal suspension due to their nature or amount.
- the surfactants are used in an amount of about 0.01 to about 15%, based on the amount of silane used.
- the process for the preparation of the colloidal suspensions can be carried out at temperatures between room temperature and 80 ° C .; the temperature range between 50 and 70 ° C. is particularly preferred.
- Aqueous dispersions of a fluorocarbon resin can be used as the perfluoroalkyl group-containing compounds.
- the chemically bound fluorine is in the form of perfluoroalkyl ligands with a chain length of 3 to 20 carbon atoms and, in addition to fluorine atoms, can contain a maximum of 1 hydrogen or chlorine atom per 2 carbon atoms.
- the perfluoroalkyl chain can also be interrupted by oxygen atoms.
- the perfluoroalkyl ligand is bound to a water-insoluble monomeric or polymeric organic compound. Examples of such compounds are polyacrylates containing perfluoroalkyl ligands (cf.
- the perfluoroalkyl group-containing dispersion contains about 5 to 50% by weight of fluorocarbon resin with a fluorine content of 0.2 to 40, preferably 1.0 to 20% by weight.
- organic solvents can also be added to the dispersion in smaller amounts in order to obtain particularly favorable behavior when applied to the fiber.
- the finish is effective on all types of fibers, i.e. fibers made of synthetic and organic and inorganic fibers and natural fibers.
- the treatment agent according to the invention is used in an amount of 0.5-2% by weight, based on the fiber material.
- finishing products can be applied either before, during or after the dyeing of the textile or subsequent further finishing steps, or subsequently after processing as a cover, upholstery or floor covering textile by treatment in the liquor, padding or spraying.
- Another method of applying the agent according to the invention to the fiber material is to use it together with a cleaning agent, especially if the textile to be treated has been soiled by use or previous processing steps. It is preferable to finish goods that have not been equipped by the manufacturer after wet cleaning by spraying the preparation onto the goods.
- the above mixture is dried, roughly crushed, ground in a powder mill and then sieved through a sieve with a mesh size of 100 ⁇ m using a sieving machine.
- the samples are loaded after the chair roller test, which is described in detail in DIN 54 324, with a total roller load of 60 kg and a change in the roller pressure direction after every 50 revolutions.
- a polyester tufted fabric (loop, 100%, PES) with a pile weight of 400 g / m 2 was treated as indicated in Example 1.
- a polyacrylic tufting fabric (loop, 100%, PAC) with a pile weight of 500 g / m 2 was treated as indicated in Example 1.
- the concentration of the equipment used was 10 g / l in all cases.
- a polyamide tufted fabric (velor, 100% PA) with a weight per square meter of 700 g was treated as indicated in Example 1.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Claims (3)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3307420 | 1983-03-03 | ||
DE19833307420 DE3307420A1 (de) | 1983-03-03 | 1983-03-03 | Textilausruestungsmittel |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0121078A1 EP0121078A1 (fr) | 1984-10-10 |
EP0121078B1 true EP0121078B1 (fr) | 1986-12-10 |
Family
ID=6192334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP19840101888 Expired EP0121078B1 (fr) | 1983-03-03 | 1984-02-23 | Produits auxiliaires textiles |
Country Status (3)
Country | Link |
---|---|
US (1) | US4781844A (fr) |
EP (1) | EP0121078B1 (fr) |
DE (2) | DE3307420A1 (fr) |
Families Citing this family (61)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3435618A1 (de) * | 1984-09-28 | 1986-04-10 | Chemische Fabrik Pfersee Gmbh, 8900 Augsburg | Verfahren zur erzielung wasch- und reinigungsbestaendiger textilausruestungen mit reaktiven (co)polymeren bzw. vorkondensaten |
EP0239108B1 (fr) * | 1986-03-28 | 1992-06-24 | Daikin Industries, Limited | Composition de démoulage |
JPS63146976A (ja) * | 1986-12-11 | 1988-06-18 | Daikin Ind Ltd | 撥水撥油剤組成物 |
US4781973A (en) * | 1987-10-22 | 1988-11-01 | General Electric Company | Fabric coating |
DE3737753A1 (de) * | 1987-11-06 | 1989-06-15 | Pfersee Chem Fab | Waessriges ausruestungsmittel und verfahren zur weichen hydrophob/oleophob-behandlung von fasermaterialien |
US4861501A (en) * | 1988-05-16 | 1989-08-29 | Basf Corporation | Stain resistant composition for synthetic organic polymer fibers and method of use: fluorocarbon polymer |
US5256318A (en) * | 1990-04-07 | 1993-10-26 | Daikin Industries Ltd. | Leather treatment and process for treating leather |
EP0467083A3 (en) * | 1990-07-14 | 1992-09-09 | Pfersee Chemie Gmbh | Perfluoroaliphatic group-containing copolymers with urethane and siloxane units |
US5258458A (en) * | 1991-02-28 | 1993-11-02 | Minnesota Mining And Manufacturing Company | Composition for providing oil and water repellency |
DE4134284A1 (de) * | 1991-10-17 | 1993-04-22 | Bayer Ag | In wasser dispergierbare blockierte polyisocyanate, verfahren zu ihrer herstellung und ihre verwendung |
US5508370A (en) * | 1991-10-17 | 1996-04-16 | Bayer Aktiengesellschaft | Water-dispersible blocked isocyanates, method of manufacture, and use thereof |
DE4201604A1 (de) * | 1992-01-22 | 1993-07-29 | Bayer Ag | Fluorhaltige copolymerisate und daraus hergestellte waessrige dispersionen |
US5387640A (en) * | 1992-01-22 | 1995-02-07 | Bayer Aktiengesellschaft | Fluorine-containing copolymers and aqueous dispersions prepared therefrom |
JPH06232379A (ja) * | 1993-02-01 | 1994-08-19 | Sharp Corp | 固体撮像素子 |
KR100290940B1 (ko) * | 1993-07-14 | 2001-11-14 | 세야 히로미치 | 옥외물품표면의처리방법 |
DE4441982A1 (de) | 1994-11-25 | 1996-05-30 | Bayer Ag | Öl-, wasser- und schmutzabweisend ausgerüstete Substrate und fluorhaltige Mittel hierzu |
CA2225526A1 (fr) * | 1995-06-23 | 1997-01-09 | Minnesota Mining And Manufacturing Company | Composition et procede permettant de conferer des proprietes repulsives durables a des substrats |
US5888290A (en) * | 1996-05-24 | 1999-03-30 | Minnesota Mining And Manufacturing Company | Composition and process for imparting durable repellency to substrates |
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US3083224A (en) * | 1961-12-08 | 1963-03-26 | Du Pont | Polyfluoroalkyl phosphates |
CH106968D (fr) * | 1965-01-21 | 1900-01-01 | ||
US3385812A (en) * | 1965-06-25 | 1968-05-28 | Du Pont | Finishing composition comprising a fluorochemical and a polyorganosiloxane |
NL6613150A (fr) * | 1966-06-03 | 1967-12-04 | ||
US3949136A (en) * | 1972-12-22 | 1976-04-06 | Ciba-Geigy Ag | Fluorine-containing organopolysiloxanes, process for their use |
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US4321403A (en) * | 1979-06-04 | 1982-03-23 | Allied Corporation | N-Methylpyrrolidone solvent in esterification of carboxybenzenes |
DE3004824A1 (de) * | 1980-02-09 | 1981-08-20 | Bayer Ag, 5090 Leverkusen | Polstabilisierendes textilimpraegniermittel |
US4473371A (en) * | 1981-09-04 | 1984-09-25 | Hoechst Aktiengesellschaft | Perfluoroalkyl esters, a process for their preparation and their use as a soil-repellant agent |
-
1983
- 1983-03-03 DE DE19833307420 patent/DE3307420A1/de not_active Withdrawn
-
1984
- 1984-02-23 DE DE8484101888T patent/DE3461660D1/de not_active Expired
- 1984-02-23 EP EP19840101888 patent/EP0121078B1/fr not_active Expired
-
1987
- 1987-05-21 US US07/053,168 patent/US4781844A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
EP0121078A1 (fr) | 1984-10-10 |
US4781844A (en) | 1988-11-01 |
DE3461660D1 (en) | 1987-01-22 |
DE3307420A1 (de) | 1984-09-13 |
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