US20090130374A1 - Stain and soil repellent composition - Google Patents
Stain and soil repellent composition Download PDFInfo
- Publication number
- US20090130374A1 US20090130374A1 US11/993,326 US99332606A US2009130374A1 US 20090130374 A1 US20090130374 A1 US 20090130374A1 US 99332606 A US99332606 A US 99332606A US 2009130374 A1 US2009130374 A1 US 2009130374A1
- Authority
- US
- United States
- Prior art keywords
- weight
- stain
- carpet
- repellent composition
- soil repellent
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 66
- 230000002940 repellent Effects 0.000 title claims abstract description 45
- 239000005871 repellent Substances 0.000 title claims abstract description 45
- 239000002689 soil Substances 0.000 title claims abstract description 30
- -1 fluorocarbon compound Chemical class 0.000 claims abstract description 27
- 239000007859 condensation product Substances 0.000 claims abstract description 23
- 150000001875 compounds Chemical class 0.000 claims abstract description 19
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims abstract description 10
- 239000004952 Polyamide Substances 0.000 claims abstract description 6
- 229920002647 polyamide Polymers 0.000 claims abstract description 6
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 14
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000004014 plasticizer Substances 0.000 claims description 10
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 9
- 239000000194 fatty acid Substances 0.000 claims description 9
- 229930195729 fatty acid Natural products 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 9
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical group OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- 239000011737 fluorine Substances 0.000 claims description 7
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 6
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 5
- 239000004088 foaming agent Substances 0.000 claims description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 4
- 229920001778 nylon Polymers 0.000 claims description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 4
- 210000002268 wool Anatomy 0.000 claims description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- 229920002292 Nylon 6 Polymers 0.000 claims description 2
- 229920002302 Nylon 6,6 Polymers 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical class CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 claims description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 229940079877 pyrogallol Drugs 0.000 claims description 2
- 125000006850 spacer group Chemical group 0.000 claims description 2
- 239000004711 α-olefin Substances 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims 2
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims 1
- 230000008021 deposition Effects 0.000 claims 1
- 238000010186 staining Methods 0.000 claims 1
- 239000006260 foam Substances 0.000 abstract description 15
- 238000000034 method Methods 0.000 abstract description 13
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 15
- 238000005187 foaming Methods 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 230000007935 neutral effect Effects 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000004677 Nylon Substances 0.000 description 3
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical class C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 238000004873 anchoring Methods 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical compound O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920003987 resole Polymers 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 125000001174 sulfone group Chemical group 0.000 description 2
- 125000000542 sulfonic acid group Chemical group 0.000 description 2
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- QUWAJPZDCZDTJS-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfonylphenol Chemical compound OC1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1O QUWAJPZDCZDTJS-UHFFFAOYSA-N 0.000 description 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical class ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 240000002989 Euphorbia neriifolia Species 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910006069 SO3H Inorganic materials 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 159000000021 acetate salts Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229950011260 betanaphthol Drugs 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-M dodecyl sulfate Chemical compound CCCCCCCCCCCCOS([O-])(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-M 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- GEPGFAGMWQJLTK-UHFFFAOYSA-N hydroxymethyl-bis(2-prop-2-enoyloxyethyl)azanium;methyl sulfate Chemical compound COS([O-])(=O)=O.C=CC(=O)OCC[NH+](CO)CCOC(=O)C=C GEPGFAGMWQJLTK-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002270 phosphoric acid ester group Chemical group 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000001993 wax Substances 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
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/41—Phenol-aldehyde or phenol-ketone resins
- D06M15/412—Phenol-aldehyde or phenol-ketone resins sulfonated
-
- 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
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/41—Phenol-aldehyde or phenol-ketone resins
-
- 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
-
- 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
- Y10T428/23907—Pile or nap type surface or component
- Y10T428/23986—With coating, impregnation, or bond
Definitions
- the present invention relates to a stain and soil repellent composition for carpets.
- the invention especially relates to a stain and soil repellent composition for carpets made from polyamide, wool and their mixtures.
- a stain repellent can be applied to a carpet in a continuous or discontinuous process, in which between 3 and 7 weight-% of the stain repellent relative to the pile weight (the weight of the utilized fiber) is used. It is also known that considerably higher concentrations, for example up to 10 weight %, can be utilized.
- a separate treatment bath is utilized after the dyeing step, in which the stain repellent is applied to the carpet at a pH between 2.5 and 7.
- the stain repellent is applied to the carpet with suitable devices, such as a waterfall applicator, immersion tank and Fluidyer® apparatus.
- a treatment with a fluorocarbon compound follows as the last finishing step, for example with a desired concentration of from 1.0 to 1.6 weight-% of fluorocarbon relative to the pile weight of the carpet.
- the application of the fluorocarbon compound typically precedes the dryer of the continuous dye unit or is prior to the coating oven.
- the simplest procedure is a spray application which is carried out with a suitable spray device.
- the fluorocarbon compound is applied as an aqueous solution to a dry or lightly moistened carpet.
- the most often-used application method is a foam application. With this system, a highly concentrated solution of the fluorocarbon compound can be applied to the carpet as a foam with minimal wetness.
- special foaming aids are added to the fluorocarbon compounds, which then degrade at the selected drying temperatures, and the fluorocarbon compound remains on the fiber and bonds to it.
- the two-step process is time consuming, relatively high cost, and resource intensive.
- the application of the stain repellent together with the fluorocarbon in a single step is advocated.
- the task of the present invention is to provide an improved stain and soil repellent composition compared to the current state of technology.
- This task was achieved according to the invention by using a combination of two different stain repellents together with a fluorocarbon compound to impart desirable stain and soil repellent properties to carpets.
- the present invention is a stain and soil repellent composition which encompasses the following components:
- hydroxyaromatic compounds are compounds which have at least one, preferably one or two, aromatic nucleus, and at least one hydroxyl group directly bound to the nucleus or one of the nuclei.
- Other substituents can be bound to the nucleus besides the hydroxyl group, for example halogens, or sulfonic acid groups.
- Ring systems with 6 to 12 carbon atoms are preferred as the aromatic nucleus, for example phenyl or naphthyl radicals with an OH group in the 1, 2, or 3 position.
- substituted and non-substituted phenol, 1-naphthol, and 2-naphthol are substituted and non-substituted phenol, 1-naphthol, and 2-naphthol.
- Hydroxyaromatic compounds with more than one hydroxyl group at the nucleus are also suitable, for example di-hydroxyaromatic compounds such as resorcinol and catechol, or tri-hydroxyaromatic compounds such as pyrogallol (1,2,3-tri-hydroxybenzol).
- di-hydroxyaromatic compounds such as resorcinol and catechol
- tri-hydroxyaromatic compounds such as pyrogallol (1,2,3-tri-hydroxybenzol).
- aromatic nuclei can also be covalently bonded over a functional group, for example a sulfone group.
- condensation products of the hydroxyl aromatic compounds with formaldehyde according to the invention are inherently easy to make and are known to those skilled in the art.
- novolak with linear chains can be obtained from an acid catalyzed reaction of excess phenol with formaldehyde, in which the phenol units are bonded with methylene bridges. Utilizing a basic catalyst and excess formaldehyde, phenol and formaldehyde are condensed to resoles.
- the aromatic adducts either already have sulfonic acid groups or they can be attached after a typical condensation, for example, through a reaction with sulfur trioxide, chlorosulphonic acid, or amidosulphonic acid.
- a condensation reaction of the OH-groups of the sulphonic acid group can occur, so that the end products of the condensation reaction do not have any free sulphonic acid groups and, therefore, can be utilized as a condensation product according to component (a) of the present invention.
- condensation products without sulphonic acid and carboxyl groups can be obtained, for example, under the name ZELAN® 8236 from DuPont, Wilmington, Del., USA.
- ZELAN® 8236 is a base catalyzed condensation product of 4,4′bis(hydroxyphenyl) sulfone and formaldehyde.
- Condensation products with sulphonic acid groups are commercially obtainable, for example, from Zschimmer & Schwarz Mohsdorf GmbH & Co., Mohsdorf, Germany under the name Zetesal NT and from CHT R. Beitlich GmbH, Tubinen, Germany under the name Rewin KBL or Rewin KF as well as Tubicoat KF.
- the essential element of the present invention is that at least one condensation product, which is free of sulphonic acid and carboxyl groups, and at least one condensation product, which is at least partially sulphonated are used together. This combination enables the application at neutral pH and yields unexpectedly improved stain repellency, as shown in the examples below.
- compositions according to the invention contain, furthermore, at least one fluorocarbon compound (c), and, if required, at least one foaming aid (d). If a commercial product is being used for the component (c), then the foaming aid may already be contained in the commercial composition, so that it does not need to be added additionally to the composition. Based on the possible inherent foam building properties of the utilized components, it is possible, that by stirring alone, the compositions can create foam, and the addition of a foaming aid (d) is, therefore, not required. However, it can be helpful to add further foaming aids (d) to the stain and soil repellent composition of this invention despite inherent foam building properties of (c).
- the fluorocarbon compound of the component (c) is utilized together with the condensation products of the components (a) and (b) to impart oil, water and soil repellent properties to the substrate.
- Anionic, cationic or non-ionic as well as amphoteric fluorine compounds are in principle used as fluorocarbon compounds, which are also commercially available.
- fluorine containing polyacrylates U.S. Pat. No. 3,574,791 and U.S. Pat. No. 4,147,851
- fluorine containing urethanes U.S. Pat. No. 3,398,182 and US 2003/0204015 A1
- Suitable fluorocarbon compounds can be obtained under the collective name Zonyl® Carpet Protector from DuPont.
- Zonyl® 19087 Zonyl® 9535, Zonyl® 555 and Zonyl® 5180.
- Zonyl® 9087 DuPont
- the production of such fluorocarbon compounds is known to those skilled in the art and can be accomplished, for example, by attaching linear fluorinated chains called fluorotelomers to organic polymers.
- fluorotelomers For example, tetrafluoroethylene (TFE) is reacted to form a fluorocarbon compound in a telomerization process.
- TFE tetrafluoroethylene
- Fluorocarbon compounds can be subdivided basically into three molecular regions.
- Perfluoroalkyl groups are responsible for soil repellency as well as hydrophobation and oleophobation.
- a spacer gives the required molecular flexibility, so that the fluorocarbon compound is soluble and/or emulsifiable.
- An anchoring and/or adhesive group ensures the permanency of the fluorocarbon compounds.
- Preferred anchoring groups are those based on urethane.
- foam builders such as alkyl amine oxides, for example Laviron 118SK, Cognis Germany GmbH & Co. KG, Dusseldorf, Germany, can be utilized as additional foaming aids for component (d).
- alpha-olefin sulfonate such as Reworyl AOS 38 or Sulfrarnin AOS 38 (Goldschmidt GmbU, Germany)
- modified lauryl sulfate such as Tubicoat ELS (CIJT R. Breitlich GmbH, Germany) and Baygard Foamer (Lanxess Europe (GmbH & Co KG, Germany) are suitable foam builders.
- Foaming aids are being utilized for foam improvement methods by adding them directly to the finishing agent, which is to be foamed.
- the stain and soil repellent compositions of the present invention are prepared in water (e) as solvent.
- At least one plasticizer (f) can be present in the compositions according to the invention.
- Polysiloxane compounds such as amino functional polydimethylsiloxane; fatty acid condensation products, such as condensation products of hydrated tallow with 2-[2-aminoethyl)-amino]ethanol; and acetate salt (CAS No. 68425-52-5) or acryl compounds such as bis[acryloxyethyl]-hydroxymethyl ammonium methyl sulfate (CAS No. 93334-15-7) are suitable in principle as plasticizers.
- a plasticizer from the above mentioned compounds or a mixture of them can be included in the composition according to the invention.
- Suitable plasticizers are commercially available, for example, Finistrol AFN (fatty acid condensation product) of Thor, Speyer, Germany, and Megasoft JET of Ciba Specialty Chemicals; Perrustol CCA (fatty acid condensation product) of Rudolf GmbH & Co. KG, Geretsried, Germany; Raniesoft TS 20 (fatty acid condensation product) of Ranie Chemie, Wiehl, Germany; Softycon N (fatty acid condensation product) Textilcolor AG, Sevelen, Switzerland; and Zefasoft NI (fatty acid condensation product) of Zschirnmer & Schwarz Mohsdorf GmbH & Co. IKG, Mohsdorf, Germany.
- At least one fluorotenside (g) can be included in the composition according to the invention. Better penetration to a carpet with the stain and soil repellent according to the invention is achieved with addition of the fluorotenside.
- Suitable fluorotensides are obtained, for example, from DuPont Specialty Chemicals under the name Zonyl®.
- anionic, cationic, non-ionic or amphoteric fluorotensides are useful in practicing the invention.
- Zonyl® FSA, FSP, FSE, UR, FSJ, FSN, FSN-100, FSO, FSO-100, FSD as well as TBS are especially suitable.
- x can take the value from 1 to 20, preferably from 1 to 10.
- compositions according to the invention can contain only a special fluorotenside or a mixture of different fluorotensides alone or in a mixture with other non-fluorine containing tensides.
- At least one blocked isocyanate group containing polymer or oligomer (h) can be used.
- Gard WEB (Rudolf GmbH & Co. KG, Germany) and Hydrophobol XAN (Ciba, Switzerland) are commercial products, which can be utilized as components (h) in the context of the present invention.
- the polymers or oligomers of these components contain at least one or more than one blocked isocyanate group, for example 2, 3, 4, 5 or more.
- compositions according to the invention can further contain customary additives (i) to reduce the cost of the composition.
- customary additives i
- the following substances can be used as additives either alone or as mixtures: siloxane; acrylate and substituted acrylate polymers and copolymers; n-methylolacrylamide containing acrylate copolymers; urethane; condensate or precondensate of urea or melamine with formaldehyde; glyoxal resins; condensate of fatty acids with melamine or urea derivatives or with polyamides and their epichlorohydrin adducts; waxes; polyethylene; chlorinated polyethylene; alkene ketene dimers, esters and amides; glycols, such as diethylene glycol; and fatty acids and their derivative and salts, such as stearic acid or stearic acid sodium salt.
- pH regulators for example, inorganic or organic acids and bases can be used.
- components (a) are present in the composition for best results according to the invention at from 0.1 to 3 weight-%, preferably at from 0.2 to 0.5 weight-%, especially preferred at from 0.2 to 0.49 weight-%.
- Components (b) are present, for example, at from 0.1 to 3 weight-%, preferably at from 0.2 to 0.5 weight-%, especially preferred at from 0.2 to 0.49 weight-%.
- Components (c) are present, for example, at from 0.5 to 3.5 weight-%, preferably at from 0.7 to 1.7 weight-%, and especially preferred at from 0.7 to 1.69 weight-%.
- Components (d) are present for example, at from 0 to 5 weight-%, preferably at from 0.05 to 0.1 weight-%, and especially preferred at from 0.05 to 0.09 weight-%.
- Components (e) are present, for example, at from 71 to 99.3 weight-%, preferably at from 91.4 to 98.84 weight-%, and especially preferred at from 91.47 to 98.83 weight-%.
- Components (f) are present, for example, at from 0 to 2% weight-%, preferably at from 0.01 to 0.1 weight-%, and especially preferred at from 0.01 to 0.09 weight-%.
- Components (g) are present, for example, at from 0 to 0.5 weight-%, preferably at from 0 to 0.2 weight-%, and especially preferred at from 0.01 to 0.2 weight-%.
- Components (h) are present, for example, at from 0 to 2.0 weight-%, preferably at from 0 to 0.5 weight-%, and especially preferred at from 0 to 0.49 weight-%.
- Components (i) are present, for example, at from 0 to 10 weight-%, preferably at from 0 to 5 weight-%, and especially preferred at from 0 to 4.99 weight-%.
- the composition of the present invention is applied at a neutral pH1, for example, between 6 and 8, and preferably between 7 and 8.
- a neutral pH1 for example, between 6 and 8, and preferably between 7 and 8.
- Components (b) alone can only be applied at an acidic pH-value, since this value is required so that they can react with the fibers and become effective.
- Components (a) alone can be applied at neutral pH value and are effective at that range.
- a mixture of (a) and (b) according to the invention results in a composition with a neutral pH range. This has a great advantage, since the application of the composition according to the invention with the preferred application method, is the last step of the total process. No rinsing step with water needs to follow. If only components (b) were to be utilized, a (strong) acid would remain on the carpet, which would lead to fiber damage with time.
- the stain repellents (a) and (b) are first mixed together then (f), and if required (g), (h) and (i) are added. At a later point in time, the mixture is stirred into water and subsequently mixed with the fluorocarbon compound (c) and if required with (d). If additional plasticizer (f) is used, then it is added preferably to the aqueous solution of (a), (b), and if required (g), (h) and (i) as well as (c) and (d).
- compositions of this invention can be offered and stored in different ways.
- all components (a) to (d) as well as if required (f) and/or (g) and/or (h) and/or (i) can be premixed, and the mixed composition can be conveniently stored in a suitable container.
- the individual components can be split into different containers and only added together just prior to or as part of the application.
- condensation products (a) and (b) and if required (f) and/or (g) and/or (h) and/or (i) can be stored together in one container, and the components (c) and (d) can be stored separately from each other and separately from (a) and (b). It is also feasible to store mixtures of components (a) to (c) and if required (f) and/or (g) and/or (h) and/or (i) in one container and to store (d) isolated from the mixture. Every conceivable combination and division into individual containers is possible. It is preferred that the components (a), (b) and (f) as well as if required (g), (h) and (i) are mixed in one container and then offered in one container. Upon application, i.e., at the time of application, the mixture is then further mixed with component (c) where (d) may be added if required.
- compositions of this invention are suitable as a stain and soil repellent for carpets, for example, tufted carpets or woven carpets made from any conceivable polyamide, especially nylon 6 and nylon 6,6. They can be utilized as well for wool carpets or carpets made from a mixture of wool and nylon, especially in the ratio of 80:20.
- compositions are particularly useful in a process of imparting stain and soil repellent properties to a carpet them.
- a mixture of all components is applied to the carpet in a foam-co-application.
- the stain repellent components (a) and (b) are applied together with fluorocarbon compounds (c) and the other required components onto the carpet as foam and not in succession, as is often the case.
- the compositions according to the invention are applied at from 0.5 to 5 weight-%, and preferably at from 0.5 to 2 weight-% relative to the pile weight of the carpet.
- a stain repellent composition according to the invention 0.25 weight-% Zelan® 8236 and 0.25 weight-% Rewin KF or Tubicoat KF were mixed with 99.5 weight-% water. Three parts by weight of this mixture were intensively mixed with a mixture consisting of 90 parts by weight of water and of 7 parts by weight of Zonyl® 9087. The pH of this mixture as measured was between 7 and 8.
- a cut pile nylon carpet (beige), 860 g/m 2 was treated one time (A) with 3 weight-% of the above described mixture in a foam co-application with a fluorocarbon compound, and (B) for comparison with a product which only contains a stain repellent, with sulphonic acid groups and a fluorocarbon compound.
- the stain repellent efficiency 24 hrs Kool-Aid test and 24 hrs. Coffee test
- the water and oil repellency as well as light fastness accordinging to ISO 105-BO2
- resilience towards alkali cleaning products WAQE-test
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)
- Polyurethanes Or Polyureas (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
- The present invention relates to a stain and soil repellent composition for carpets. The invention especially relates to a stain and soil repellent composition for carpets made from polyamide, wool and their mixtures.
- During the production of carpets, various stain and soil repellent chemicals are often applied. The application is typically carried out in two steps with the application of the stain repellent being first, followed by a treatment with a fluorocarbon compound.
- A stain repellent can be applied to a carpet in a continuous or discontinuous process, in which between 3 and 7 weight-% of the stain repellent relative to the pile weight (the weight of the utilized fiber) is used. It is also known that considerably higher concentrations, for example up to 10 weight %, can be utilized.
- In the discontinuous application, a separate treatment bath is utilized after the dyeing step, in which the stain repellent is applied to the carpet at a pH between 2.5 and 7.
- In the continuous application, the stain repellent is applied to the carpet with suitable devices, such as a waterfall applicator, immersion tank and Fluidyer® apparatus.
- After the application of the stain repellent, a treatment with a fluorocarbon compound follows as the last finishing step, for example with a desired concentration of from 1.0 to 1.6 weight-% of fluorocarbon relative to the pile weight of the carpet. The application of the fluorocarbon compound typically precedes the dryer of the continuous dye unit or is prior to the coating oven. The simplest procedure is a spray application which is carried out with a suitable spray device. The fluorocarbon compound is applied as an aqueous solution to a dry or lightly moistened carpet. The most often-used application method is a foam application. With this system, a highly concentrated solution of the fluorocarbon compound can be applied to the carpet as a foam with minimal wetness. For the foam creation, special foaming aids are added to the fluorocarbon compounds, which then degrade at the selected drying temperatures, and the fluorocarbon compound remains on the fiber and bonds to it.
- The two-step process is time consuming, relatively high cost, and resource intensive. Thus, the application of the stain repellent together with the fluorocarbon in a single step is advocated.
- For example US2003/0204015 A1 reveals that a mixture containing a sulphonated condensation product of phenol and formaldehyde and other compounds as stain repellent, and fluorocarbon compounds can be applied to the fibers.
- The application of stain repellent based on resole together with fluorinated, oil, water and/or soil repellent substances on a polyamide substrate is disclosed in U.S. Pat. No. 5,447,755.
- However, there is still a need for improved stain and soil repellent compositions for one-step application. Therefore, the task of the present invention is to provide an improved stain and soil repellent composition compared to the current state of technology.
- This task was achieved according to the invention by using a combination of two different stain repellents together with a fluorocarbon compound to impart desirable stain and soil repellent properties to carpets.
- The present invention is a stain and soil repellent composition which encompasses the following components:
-
- (a) a first condensation product of hydroxyaromatic compounds with formaldehyde, which is free of sulphonic acid and carboxylic groups,
- (b) a second condensation product of hydroxyaromatic compounds with formaldehyde, which is at least partially sulphonated,
- (c) at least one fluorocarbon compound,
- (d) at least one foaming agent, in case that (c) has no foam building properties,
- (e) water,
- (f) if required at least one plasticizer,
- (g) if required at least one fluorine containing surfactant,
- (h) if required at least one blocked isocyanate group containing polymer or oligomer, and
- (i) if required additional additives.
- According to the invention, hydroxyaromatic compounds are compounds which have at least one, preferably one or two, aromatic nucleus, and at least one hydroxyl group directly bound to the nucleus or one of the nuclei. Other substituents can be bound to the nucleus besides the hydroxyl group, for example halogens, or sulfonic acid groups. Ring systems with 6 to 12 carbon atoms are preferred as the aromatic nucleus, for example phenyl or naphthyl radicals with an OH group in the 1, 2, or 3 position. Especially suited are substituted and non-substituted phenol, 1-naphthol, and 2-naphthol. Hydroxyaromatic compounds with more than one hydroxyl group at the nucleus are also suitable, for example di-hydroxyaromatic compounds such as resorcinol and catechol, or tri-hydroxyaromatic compounds such as pyrogallol (1,2,3-tri-hydroxybenzol). Several aromatic nuclei can also be covalently bonded over a functional group, for example a sulfone group.
- The condensation products of the hydroxyl aromatic compounds with formaldehyde according to the invention are inherently easy to make and are known to those skilled in the art. For example, novolak with linear chains can be obtained from an acid catalyzed reaction of excess phenol with formaldehyde, in which the phenol units are bonded with methylene bridges. Utilizing a basic catalyst and excess formaldehyde, phenol and formaldehyde are condensed to resoles. To obtain condensation products with sulfone groups at the aromatic nucleus, the aromatic adducts either already have sulfonic acid groups or they can be attached after a typical condensation, for example, through a reaction with sulfur trioxide, chlorosulphonic acid, or amidosulphonic acid. If the adducts already contain sulphonic acid groups, a condensation reaction of the OH-groups of the sulphonic acid group can occur, so that the end products of the condensation reaction do not have any free sulphonic acid groups and, therefore, can be utilized as a condensation product according to component (a) of the present invention.
- Commercial condensation products without sulphonic acid and carboxyl groups can be obtained, for example, under the name ZELAN® 8236 from DuPont, Wilmington, Del., USA. ZELAN® 8236 is a base catalyzed condensation product of 4,4′bis(hydroxyphenyl) sulfone and formaldehyde. Condensation products with sulphonic acid groups are commercially obtainable, for example, from Zschimmer & Schwarz Mohsdorf GmbH & Co., Mohsdorf, Germany under the name Zetesal NT and from CHT R. Beitlich GmbH, Tubinen, Germany under the name Rewin KBL or Rewin KF as well as Tubicoat KF.
- The essential element of the present invention is that at least one condensation product, which is free of sulphonic acid and carboxyl groups, and at least one condensation product, which is at least partially sulphonated are used together. This combination enables the application at neutral pH and yields unexpectedly improved stain repellency, as shown in the examples below.
- The compositions according to the invention contain, furthermore, at least one fluorocarbon compound (c), and, if required, at least one foaming aid (d). If a commercial product is being used for the component (c), then the foaming aid may already be contained in the commercial composition, so that it does not need to be added additionally to the composition. Based on the possible inherent foam building properties of the utilized components, it is possible, that by stirring alone, the compositions can create foam, and the addition of a foaming aid (d) is, therefore, not required. However, it can be helpful to add further foaming aids (d) to the stain and soil repellent composition of this invention despite inherent foam building properties of (c).
- The fluorocarbon compound of the component (c) is utilized together with the condensation products of the components (a) and (b) to impart oil, water and soil repellent properties to the substrate. Anionic, cationic or non-ionic as well as amphoteric fluorine compounds are in principle used as fluorocarbon compounds, which are also commercially available. For example, fluorine containing polyacrylates (U.S. Pat. No. 3,574,791 and U.S. Pat. No. 4,147,851) and fluorine containing urethanes (U.S. Pat. No. 3,398,182 and US 2003/0204015 A1) can be utilized. Suitable fluorocarbon compounds can be obtained under the collective name Zonyl® Carpet Protector from DuPont. These include, for example, Zonyl® 19087, Zonyl® 9535, Zonyl® 555 and Zonyl® 5180. An example of a commercial anionic fluorocarbon compound is Zonyl® 9087 (DuPont). The production of such fluorocarbon compounds is known to those skilled in the art and can be accomplished, for example, by attaching linear fluorinated chains called fluorotelomers to organic polymers. For example, tetrafluoroethylene (TFE) is reacted to form a fluorocarbon compound in a telomerization process. Fluorocarbon compounds can be subdivided basically into three molecular regions. Perfluoroalkyl groups are responsible for soil repellency as well as hydrophobation and oleophobation. A spacer gives the required molecular flexibility, so that the fluorocarbon compound is soluble and/or emulsifiable. An anchoring and/or adhesive group ensures the permanency of the fluorocarbon compounds. Preferred anchoring groups are those based on urethane.
- Commercial foam builders such as alkyl amine oxides, for example Laviron 118SK, Cognis Germany GmbH & Co. KG, Dusseldorf, Germany, can be utilized as additional foaming aids for component (d). Furthermore, alpha-olefin sulfonate, such as Reworyl AOS 38 or Sulfrarnin AOS 38 (Goldschmidt GmbU, Germany); and modified lauryl sulfate, such as Tubicoat ELS (CIJT R. Breitlich GmbH, Germany) and Baygard Foamer (Lanxess Europe (GmbH & Co KG, Germany) are suitable foam builders.
- Foaming aids are being utilized for foam improvement methods by adding them directly to the finishing agent, which is to be foamed.
- The stain and soil repellent compositions of the present invention are prepared in water (e) as solvent.
- At least one plasticizer (f) can be present in the compositions according to the invention. Polysiloxane compounds, such as amino functional polydimethylsiloxane; fatty acid condensation products, such as condensation products of hydrated tallow with 2-[2-aminoethyl)-amino]ethanol; and acetate salt (CAS No. 68425-52-5) or acryl compounds such as bis[acryloxyethyl]-hydroxymethyl ammonium methyl sulfate (CAS No. 93334-15-7) are suitable in principle as plasticizers. A plasticizer from the above mentioned compounds or a mixture of them can be included in the composition according to the invention. Suitable plasticizers are commercially available, for example, Finistrol AFN (fatty acid condensation product) of Thor, Speyer, Germany, and Megasoft JET of Ciba Specialty Chemicals; Perrustol CCA (fatty acid condensation product) of Rudolf GmbH & Co. KG, Geretsried, Germany; Raniesoft TS 20 (fatty acid condensation product) of Ranie Chemie, Wiehl, Germany; Softycon N (fatty acid condensation product) Textilcolor AG, Sevelen, Switzerland; and Zefasoft NI (fatty acid condensation product) of Zschirnmer & Schwarz Mohsdorf GmbH & Co. IKG, Mohsdorf, Germany.
- At least one fluorotenside (g) can be included in the composition according to the invention. Better penetration to a carpet with the stain and soil repellent according to the invention is achieved with addition of the fluorotenside. Suitable fluorotensides are obtained, for example, from DuPont Specialty Chemicals under the name Zonyl®. In principle, anionic, cationic, non-ionic or amphoteric fluorotensides are useful in practicing the invention. Zonyl® FSA, FSP, FSE, UR, FSJ, FSN, FSN-100, FSO, FSO-100, FSD as well as TBS are especially suitable. In general, compounds with a hydrophobic portion of the formula CnF2n+1 and a hydrophilic portion, for example, containing carboxylic acid or carboxylic acid ester groups, phosphate or phosphoric acid ester groups, ether groups, or sulphonic acid groups are suitable. Especially suitable are the compounds with the following formulas, whereby Rf represents F(CF2CF2)2 where a=2 to 10, preferably 3 to 8:
-
RfCH2CH2SCH2CH2CO2Li, -
(RfCH2CH2O)P(O)(ONH4)2, -
(RfCH2CH2O)2P(O)(ONH4), -
(RfCH2CH2O)P(O)OH2, -
(RfCH2CO2O)2P(O)OH, -
RfCH2CH2O(CH2CH2O)xH, -
RfCH2CH2SO3H. - whereby x can take the value from 1 to 20, preferably from 1 to 10.
- The compositions according to the invention can contain only a special fluorotenside or a mixture of different fluorotensides alone or in a mixture with other non-fluorine containing tensides. Non-fluorine containing tensides contain a hydrophobic portion, for example, C2H2n+1 with n=1 to 20.
- Furthermore, at least one blocked isocyanate group containing polymer or oligomer (h) can be used. Preferred are polyisoyanates. Gard WEB (Rudolf GmbH & Co. KG, Germany) and Hydrophobol XAN (Ciba, Switzerland) are commercial products, which can be utilized as components (h) in the context of the present invention. The polymers or oligomers of these components contain at least one or more than one blocked isocyanate group, for example 2, 3, 4, 5 or more.
- The compositions according to the invention can further contain customary additives (i) to reduce the cost of the composition. For example, the following substances can be used as additives either alone or as mixtures: siloxane; acrylate and substituted acrylate polymers and copolymers; n-methylolacrylamide containing acrylate copolymers; urethane; condensate or precondensate of urea or melamine with formaldehyde; glyoxal resins; condensate of fatty acids with melamine or urea derivatives or with polyamides and their epichlorohydrin adducts; waxes; polyethylene; chlorinated polyethylene; alkene ketene dimers, esters and amides; glycols, such as diethylene glycol; and fatty acids and their derivative and salts, such as stearic acid or stearic acid sodium salt. Furthermore, pH regulators, for example, inorganic or organic acids and bases can be used. Also surface-active substances and/or dispersion agents can be used in the composition.
- The components (a) are present in the composition for best results according to the invention at from 0.1 to 3 weight-%, preferably at from 0.2 to 0.5 weight-%, especially preferred at from 0.2 to 0.49 weight-%. Components (b) are present, for example, at from 0.1 to 3 weight-%, preferably at from 0.2 to 0.5 weight-%, especially preferred at from 0.2 to 0.49 weight-%. Components (c) are present, for example, at from 0.5 to 3.5 weight-%, preferably at from 0.7 to 1.7 weight-%, and especially preferred at from 0.7 to 1.69 weight-%. Components (d) are present for example, at from 0 to 5 weight-%, preferably at from 0.05 to 0.1 weight-%, and especially preferred at from 0.05 to 0.09 weight-%. Components (e) are present, for example, at from 71 to 99.3 weight-%, preferably at from 91.4 to 98.84 weight-%, and especially preferred at from 91.47 to 98.83 weight-%. Components (f) are present, for example, at from 0 to 2% weight-%, preferably at from 0.01 to 0.1 weight-%, and especially preferred at from 0.01 to 0.09 weight-%. Components (g) are present, for example, at from 0 to 0.5 weight-%, preferably at from 0 to 0.2 weight-%, and especially preferred at from 0.01 to 0.2 weight-%. Components (h) are present, for example, at from 0 to 2.0 weight-%, preferably at from 0 to 0.5 weight-%, and especially preferred at from 0 to 0.49 weight-%. Components (i) are present, for example, at from 0 to 10 weight-%, preferably at from 0 to 5 weight-%, and especially preferred at from 0 to 4.99 weight-%.
- In contrast to the traditional stain and soil repellent compositions, the composition of the present invention is applied at a neutral pH1, for example, between 6 and 8, and preferably between 7 and 8. The pH results when all of the individual components are mixed together.
- Components (b) alone can only be applied at an acidic pH-value, since this value is required so that they can react with the fibers and become effective. Components (a) alone, however, can be applied at neutral pH value and are effective at that range. A mixture of (a) and (b) according to the invention results in a composition with a neutral pH range. This has a great advantage, since the application of the composition according to the invention with the preferred application method, is the last step of the total process. No rinsing step with water needs to follow. If only components (b) were to be utilized, a (strong) acid would remain on the carpet, which would lead to fiber damage with time.
- The alternative utilization of components (a) alone, according to the present invention, is not possible at a neutral pH value in the preferred foam application process, since (a) is not compatible with foaming agents. Only mixing of components (a) and (b) is surprisingly possible in the foam application procedure.
- In the production of the compositions according to the invention, the stain repellents (a) and (b) are first mixed together then (f), and if required (g), (h) and (i) are added. At a later point in time, the mixture is stirred into water and subsequently mixed with the fluorocarbon compound (c) and if required with (d). If additional plasticizer (f) is used, then it is added preferably to the aqueous solution of (a), (b), and if required (g), (h) and (i) as well as (c) and (d). If larger quantities of the plasticizer, for example more than 2 parts (f), are added directly into the products (a), (b) or (c) and (d), (i.e., in concentrated, not water diluted form), then poorer results in terms of lower stain and soil repellancy are generally obtained.
- The compositions of this invention can be offered and stored in different ways. On the one hand, all components (a) to (d) as well as if required (f) and/or (g) and/or (h) and/or (i) can be premixed, and the mixed composition can be conveniently stored in a suitable container. On the other hand, the individual components can be split into different containers and only added together just prior to or as part of the application.
- For example, the condensation products (a) and (b) and if required (f) and/or (g) and/or (h) and/or (i) can be stored together in one container, and the components (c) and (d) can be stored separately from each other and separately from (a) and (b). It is also feasible to store mixtures of components (a) to (c) and if required (f) and/or (g) and/or (h) and/or (i) in one container and to store (d) isolated from the mixture. Every conceivable combination and division into individual containers is possible. It is preferred that the components (a), (b) and (f) as well as if required (g), (h) and (i) are mixed in one container and then offered in one container. Upon application, i.e., at the time of application, the mixture is then further mixed with component (c) where (d) may be added if required.
- The compositions of this invention are suitable as a stain and soil repellent for carpets, for example, tufted carpets or woven carpets made from any conceivable polyamide, especially nylon 6 and nylon 6,6. They can be utilized as well for wool carpets or carpets made from a mixture of wool and nylon, especially in the ratio of 80:20.
- The compositions are particularly useful in a process of imparting stain and soil repellent properties to a carpet them. In the process, a mixture of all components is applied to the carpet in a foam-co-application. The stain repellent components (a) and (b) are applied together with fluorocarbon compounds (c) and the other required components onto the carpet as foam and not in succession, as is often the case. The compositions according to the invention are applied at from 0.5 to 5 weight-%, and preferably at from 0.5 to 2 weight-% relative to the pile weight of the carpet.
- The invention is explained with the following examples to a greater extent, without it being limited by them.
- Production of a stain repellent composition according to the invention: 0.25 weight-% Zelan® 8236 and 0.25 weight-% Rewin KF or Tubicoat KF were mixed with 99.5 weight-% water. Three parts by weight of this mixture were intensively mixed with a mixture consisting of 90 parts by weight of water and of 7 parts by weight of Zonyl® 9087. The pH of this mixture as measured was between 7 and 8.
- Treatment of a carpet:
- A cut pile nylon carpet (beige), 860 g/m2 was treated one time (A) with 3 weight-% of the above described mixture in a foam co-application with a fluorocarbon compound, and (B) for comparison with a product which only contains a stain repellent, with sulphonic acid groups and a fluorocarbon compound. After drying, the stain repellent efficiency (24 hrs Kool-Aid test and 24 hrs. Coffee test), the water and oil repellency as well as light fastness (according to ISO 105-BO2), and resilience towards alkali cleaning products (WAQE-test) were tested. The results are summarized in the following table:
-
24 hrs WAQE TEST 24 hrs Kool- Coffee Water Oil Light sodium lauryl Aid Rinsed Cleaned Repellency Repellency Fastness Sulfate Scale 1-10 1-10 1-6 1-6 1-8 1-10 Aim >=9-10 >=8-9 >=8-9 >=3 >=4-5 >=6 (A) 10 9 3 2 5-6 9 (B) 9 7 3 2 5 — - Excellent results were obtained with the stain and soil repellent composition according to the invention as compared to a traditional stain and soil repellent composition which only contain one stain repellent with sulphonic acid groups. The stain repellent properties of a nylon carpet sample treated with a composition according to the invention corresponded to the upper level of the scale of desired values.
Claims (15)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE05106523.3 | 2005-07-15 | ||
| EP20050106523 EP1746199B1 (en) | 2005-07-15 | 2005-07-15 | Soil release and stain resistance composition |
| PCT/US2006/025142 WO2007011506A1 (en) | 2005-07-15 | 2006-06-28 | Stain and soil repellent composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20090130374A1 true US20090130374A1 (en) | 2009-05-21 |
Family
ID=35431798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/993,326 Abandoned US20090130374A1 (en) | 2005-07-15 | 2006-06-28 | Stain and soil repellent composition |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20090130374A1 (en) |
| EP (2) | EP1746199B1 (en) |
| CN (1) | CN101273167A (en) |
| AT (2) | ATE373137T1 (en) |
| AU (1) | AU2006270387A1 (en) |
| CA (1) | CA2612898A1 (en) |
| DE (2) | DE502005001498D1 (en) |
| RS (1) | RS51538B (en) |
| WO (1) | WO2007011506A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020084457A1 (en) * | 2018-10-24 | 2020-04-30 | Invista Textiles (U.K.) Limited | Method and products to impart stain protection |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103282570A (en) * | 2010-11-12 | 2013-09-04 | 英威达技术有限公司 | Spray-on anti-oil formulations for fibers, carpets and fabrics |
| CA3119089A1 (en) * | 2018-11-27 | 2020-06-04 | Toray Industries, Inc. | Carpet |
Citations (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3398182A (en) * | 1962-06-22 | 1968-08-20 | Minnesota Mining & Mfg | Fluorocarbon urethane compounds |
| US3574791A (en) * | 1967-02-09 | 1971-04-13 | Minnesota Mining & Mfg | Block and graft copolymers containing water-solvatable polar groups and fluoroaliphatic groups |
| US4147851A (en) * | 1978-06-13 | 1979-04-03 | E. I. Du Pont De Nemours And Company | Fluorine-containing oil- and water-repellant copolymers |
| US4680212A (en) * | 1986-03-06 | 1987-07-14 | Monsanto Company | Stain resistant nylon fibers |
| US5073442A (en) * | 1989-09-05 | 1991-12-17 | Trichromatic Carpet Inc. | Method of enhancing the soil- and stain-resistance characteristics of polyamide and wool fabrics, the fabrics so treated, and treating compositions |
| US5447755A (en) * | 1993-02-02 | 1995-09-05 | E. I. Du Pont De Nemours And Company | Substrates treated with bis(hydroxyphenyl) sulfone stain-resists |
| US5708087A (en) * | 1996-02-23 | 1998-01-13 | E. I. Du Pont De Nemours And Company | Carboxylic acid-containing polymer/resole stain-resists |
| US5725889A (en) * | 1996-09-18 | 1998-03-10 | E. I. Du Pont De Nemours And Company | Phenolic stain-resists |
| US6280648B1 (en) * | 1998-10-20 | 2001-08-28 | Sybron Chemicals, Inc. | Stain resistant composition for polyamide containing substrates |
| US20010027581A1 (en) * | 2000-03-10 | 2001-10-11 | Yanhui Sun | Dyeable and stain resistant nylon carpet treatment |
| US20020144353A1 (en) * | 2000-07-03 | 2002-10-10 | Markus Baumann | Method of after-treatment of a dyeable nylon textile surface with a stain resist and the article produced thereby |
| US20020148049A1 (en) * | 1999-07-08 | 2002-10-17 | Markus Baumann | Method of imparting stain resistance to a differentially dyeable textile surface and the article produced thereby |
| US20030204015A1 (en) * | 2002-04-17 | 2003-10-30 | Burleigh Malcolm B. | Repellent fluorochemical compositions |
| US7276085B2 (en) * | 2003-07-24 | 2007-10-02 | Shaw Industries Group, Inc. | Methods of treating and cleaning fibers, carpet yarns and carpets |
| US7279013B2 (en) * | 1999-12-17 | 2007-10-09 | Trichromatic Carpet Inc. | Polyamide fiber substrate having stain resistance, composition and method |
| US20080287020A1 (en) * | 2007-05-18 | 2008-11-20 | Rudat Martin A | Method and composition for treating fibrous substrates |
| US7785374B2 (en) * | 2005-01-24 | 2010-08-31 | Columbia Insurance Co. | Methods and compositions for imparting stain resistance to nylon materials |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU646269B2 (en) * | 1990-06-12 | 1994-02-17 | E.I. Du Pont De Nemours And Company | Stain-resistant fabrics |
-
2005
- 2005-07-15 AT AT05106523T patent/ATE373137T1/en active
- 2005-07-15 DE DE200550001498 patent/DE502005001498D1/en not_active Expired - Lifetime
- 2005-07-15 EP EP20050106523 patent/EP1746199B1/en not_active Expired - Lifetime
-
2006
- 2006-06-28 RS RSP20110004 patent/RS51538B/en unknown
- 2006-06-28 EP EP20060785727 patent/EP1924735B1/en active Active
- 2006-06-28 AT AT06785727T patent/ATE488637T1/en not_active IP Right Cessation
- 2006-06-28 DE DE200660018326 patent/DE602006018326D1/en active Active
- 2006-06-28 WO PCT/US2006/025142 patent/WO2007011506A1/en not_active Ceased
- 2006-06-28 US US11/993,326 patent/US20090130374A1/en not_active Abandoned
- 2006-06-28 CN CNA2006800257989A patent/CN101273167A/en active Pending
- 2006-06-28 AU AU2006270387A patent/AU2006270387A1/en not_active Abandoned
- 2006-06-28 CA CA 2612898 patent/CA2612898A1/en not_active Abandoned
Patent Citations (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3398182A (en) * | 1962-06-22 | 1968-08-20 | Minnesota Mining & Mfg | Fluorocarbon urethane compounds |
| US3574791A (en) * | 1967-02-09 | 1971-04-13 | Minnesota Mining & Mfg | Block and graft copolymers containing water-solvatable polar groups and fluoroaliphatic groups |
| US4147851A (en) * | 1978-06-13 | 1979-04-03 | E. I. Du Pont De Nemours And Company | Fluorine-containing oil- and water-repellant copolymers |
| US4680212A (en) * | 1986-03-06 | 1987-07-14 | Monsanto Company | Stain resistant nylon fibers |
| US5073442A (en) * | 1989-09-05 | 1991-12-17 | Trichromatic Carpet Inc. | Method of enhancing the soil- and stain-resistance characteristics of polyamide and wool fabrics, the fabrics so treated, and treating compositions |
| US5447755A (en) * | 1993-02-02 | 1995-09-05 | E. I. Du Pont De Nemours And Company | Substrates treated with bis(hydroxyphenyl) sulfone stain-resists |
| US5708087A (en) * | 1996-02-23 | 1998-01-13 | E. I. Du Pont De Nemours And Company | Carboxylic acid-containing polymer/resole stain-resists |
| US5725889A (en) * | 1996-09-18 | 1998-03-10 | E. I. Du Pont De Nemours And Company | Phenolic stain-resists |
| US6280648B1 (en) * | 1998-10-20 | 2001-08-28 | Sybron Chemicals, Inc. | Stain resistant composition for polyamide containing substrates |
| US6852134B2 (en) * | 1999-07-08 | 2005-02-08 | Invista North America S.A.R.L. | Method of imparting stain resistance to a differentially dyeable textile surface and the article produced thereby |
| US20020148049A1 (en) * | 1999-07-08 | 2002-10-17 | Markus Baumann | Method of imparting stain resistance to a differentially dyeable textile surface and the article produced thereby |
| US20040123398A1 (en) * | 1999-07-08 | 2004-07-01 | Markus Baumann | Method of imparting stain resistance |
| US7279013B2 (en) * | 1999-12-17 | 2007-10-09 | Trichromatic Carpet Inc. | Polyamide fiber substrate having stain resistance, composition and method |
| US20010027581A1 (en) * | 2000-03-10 | 2001-10-11 | Yanhui Sun | Dyeable and stain resistant nylon carpet treatment |
| US20020144353A1 (en) * | 2000-07-03 | 2002-10-10 | Markus Baumann | Method of after-treatment of a dyeable nylon textile surface with a stain resist and the article produced thereby |
| US6811574B2 (en) * | 2000-07-03 | 2004-11-02 | Dupont Textiles & Interiors, Inc. | Method of after-treatment of a dyeable nylon textile surface with a stain resist and the article produced thereby |
| US20040123399A1 (en) * | 2000-07-03 | 2004-07-01 | Markus Baumann | Method of after-treatment of a dyeable nylon textile surface with a stain resist and the article produced thereby |
| US20050198743A1 (en) * | 2000-07-03 | 2005-09-15 | Dupont Textiles & Interiors, Inc. | Method of after-treatment of dyeable nylon textile surface with a stain resist and the article produced thereby |
| US20030204015A1 (en) * | 2002-04-17 | 2003-10-30 | Burleigh Malcolm B. | Repellent fluorochemical compositions |
| US7276085B2 (en) * | 2003-07-24 | 2007-10-02 | Shaw Industries Group, Inc. | Methods of treating and cleaning fibers, carpet yarns and carpets |
| US7488351B2 (en) * | 2003-07-24 | 2009-02-10 | Columbia Insurance Company | Methods of treating and cleaning fibers, carpet yarns and carpets |
| US7785374B2 (en) * | 2005-01-24 | 2010-08-31 | Columbia Insurance Co. | Methods and compositions for imparting stain resistance to nylon materials |
| US20080287020A1 (en) * | 2007-05-18 | 2008-11-20 | Rudat Martin A | Method and composition for treating fibrous substrates |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020084457A1 (en) * | 2018-10-24 | 2020-04-30 | Invista Textiles (U.K.) Limited | Method and products to impart stain protection |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007011506A1 (en) | 2007-01-25 |
| EP1924735A1 (en) | 2008-05-28 |
| EP1924735B1 (en) | 2010-11-17 |
| ATE488637T1 (en) | 2010-12-15 |
| DE602006018326D1 (en) | 2010-12-30 |
| DE502005001498D1 (en) | 2007-10-25 |
| EP1746199A1 (en) | 2007-01-24 |
| CA2612898A1 (en) | 2007-01-25 |
| EP1746199B1 (en) | 2007-09-12 |
| RS51538B (en) | 2011-06-30 |
| CN101273167A (en) | 2008-09-24 |
| AU2006270387A1 (en) | 2007-01-25 |
| ATE373137T1 (en) | 2007-09-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6129296B2 (en) | Fluorochemical compounds, compositions, articles, and methods | |
| US6582620B2 (en) | Water-soluble, water/oil repellent treating composition and method of making | |
| KR20170026578A (en) | Fluorinecontaining waterrepellent composition | |
| US20090233507A1 (en) | Fabric treatment process | |
| GB2260995A (en) | Soil and stain resistance of fabrics | |
| JP2020056031A (en) | Water-repellent and antifouling fluorine-free composition | |
| AU2015243869A1 (en) | Water repellent, soil resistant, fluorine-free compositions | |
| EP1924735B1 (en) | Stain and soil repellent composition | |
| CN103649407A (en) | Fluorinated soil resist compositions | |
| RS50507B (en) | MEASURES FOR PROTECTION AGAINST DEATH AND Dirt | |
| AU2008319193B2 (en) | Soil resist additive | |
| MXPA06010894A (en) | Fluorochemical composition and method for treating a substrate therewith. | |
| KR20160061366A (en) | Polysiloxanes with quaternized heterocyclic groups | |
| AU2017201736B2 (en) | Spray-on anti-soil formulations for fibers, carpets and fabrics | |
| US20100291340A1 (en) | Method For Imparting Bleach And Stain Resistance To Dyed Yarns In Carpet And Products Made Therewith | |
| KR20120042873A (en) | Method to impart soil resistance to a substrate | |
| US20010044973A1 (en) | Leather treatment | |
| EP1094147A1 (en) | Enhancement of the wet sliding property of textile material and a wet sliding agent therefore | |
| WO2020084457A1 (en) | Method and products to impart stain protection | |
| KR20120092093A (en) | 1,3 - propanediol soil resist compositions | |
| MXPA99009029A (en) | Mixed fluorochemical hydrocarbon condensates to impart oil and water repellency to a substrate | |
| KR20070016135A (en) | Fluorocompound composition and processing method of substrate using the same |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: INVISTA NORTH AMERICA S.A.R.L., DELAWARE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:BAUMANNI, MARKUS;REEL/FRAME:020768/0264 Effective date: 20080331 |
|
| AS | Assignment |
Owner name: JPMORGAN CHASE BANK, N.A.,NEW YORK Free format text: SECURITY AGREEMENT;ASSIGNOR:INVISTA NORTH AMERICA, S.A.R.L.;REEL/FRAME:021199/0782 Effective date: 20080623 Owner name: JPMORGAN CHASE BANK, N.A., NEW YORK Free format text: SECURITY AGREEMENT;ASSIGNOR:INVISTA NORTH AMERICA, S.A.R.L.;REEL/FRAME:021199/0782 Effective date: 20080623 |
|
| AS | Assignment |
Owner name: DEUTSCHE BANK AG NEW YORK BRANCH, AS COLLATERAL AG Free format text: SECURITY AGREEMENT;ASSIGNOR:INVISTA NORTH AMERICA S.A.R.L.;REEL/FRAME:022416/0849 Effective date: 20090206 Owner name: INVISTA NORTH AMERICA S.A.R.L. (F/K/A ARTEVA NORTH Free format text: RELEASE OF U.S. PATENT SECURITY INTEREST;ASSIGNOR:JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT (F/K/A JPMORGAN CHASE BANK);REEL/FRAME:022427/0001 Effective date: 20090206 |
|
| AS | Assignment |
Owner name: INVISTA NORTH AMERICA S.A.R.L., NORTH CAROLINA Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:DEUTSCHE BANK AG NEW YORK BRANCH;REEL/FRAME:027211/0298 Effective date: 20111110 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |