GB2366568A - Method of treating fabric - Google Patents
Method of treating fabric Download PDFInfo
- Publication number
- GB2366568A GB2366568A GB0021481A GB0021481A GB2366568A GB 2366568 A GB2366568 A GB 2366568A GB 0021481 A GB0021481 A GB 0021481A GB 0021481 A GB0021481 A GB 0021481A GB 2366568 A GB2366568 A GB 2366568A
- Authority
- GB
- United Kingdom
- Prior art keywords
- fabric
- composition
- cross
- monomer
- weight
- 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.)
- Withdrawn
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 144
- 238000000034 method Methods 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 claims abstract description 92
- 239000000178 monomer Substances 0.000 claims abstract description 38
- 238000001035 drying Methods 0.000 claims abstract description 21
- 229920006037 cross link polymer Polymers 0.000 claims abstract description 15
- 238000009736 wetting Methods 0.000 claims abstract description 6
- 238000011282 treatment Methods 0.000 claims description 17
- 238000004900 laundering Methods 0.000 claims description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000004753 textile Substances 0.000 claims description 12
- 239000003431 cross linking reagent Substances 0.000 claims description 10
- 239000003999 initiator Substances 0.000 claims description 10
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 9
- 150000003839 salts Chemical class 0.000 claims description 9
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical group NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 229960005070 ascorbic acid Drugs 0.000 claims description 5
- 235000010323 ascorbic acid Nutrition 0.000 claims description 5
- 239000011668 ascorbic acid Substances 0.000 claims description 5
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 4
- 125000005395 methacrylic acid group Chemical class 0.000 claims description 4
- 239000002304 perfume Substances 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical group COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 3
- 150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 3
- 238000005507 spraying Methods 0.000 claims description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- 150000003926 acrylamides Chemical class 0.000 claims description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
- 150000001253 acrylic acids Chemical class 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 150000003440 styrenes Chemical class 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- 229920001567 vinyl ester resin Polymers 0.000 claims description 2
- 150000004040 pyrrolidinones Chemical class 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 29
- 229920000642 polymer Polymers 0.000 description 17
- 229920000742 Cotton Polymers 0.000 description 15
- 241000219146 Gossypium Species 0.000 description 15
- 239000000463 material Substances 0.000 description 15
- 125000000217 alkyl group Chemical group 0.000 description 13
- 125000002091 cationic group Chemical group 0.000 description 13
- 239000003599 detergent Substances 0.000 description 11
- -1 acrylate ester Chemical class 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- 150000004665 fatty acids Chemical class 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 230000003750 conditioning effect Effects 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 125000001453 quaternary ammonium group Chemical group 0.000 description 6
- 239000003381 stabilizer Substances 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 5
- 238000010409 ironing Methods 0.000 description 5
- 239000004902 Softening Agent Substances 0.000 description 4
- 229910000323 aluminium silicate Inorganic materials 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 229940048053 acrylate Drugs 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 239000003945 anionic surfactant Substances 0.000 description 3
- 230000001153 anti-wrinkle effect Effects 0.000 description 3
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 238000002791 soaking Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- ZEYUSQVGRCPBPG-UHFFFAOYSA-N 4,5-dihydroxy-1,3-bis(hydroxymethyl)imidazolidin-2-one Chemical compound OCN1C(O)C(O)N(CO)C1=O ZEYUSQVGRCPBPG-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- 102100026735 Coagulation factor VIII Human genes 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 2
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 2
- 229910000503 Na-aluminosilicate Inorganic materials 0.000 description 2
- 108010081873 Persil Proteins 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- UMSVPCYSAUKCAZ-UHFFFAOYSA-N propane;hydrochloride Chemical compound Cl.CCC UMSVPCYSAUKCAZ-UHFFFAOYSA-N 0.000 description 2
- 235000012217 sodium aluminium silicate Nutrition 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- FXXMDJFRMDVSCF-RXSVEWSESA-N (2r)-2-[(1s)-1,2-dihydroxyethyl]-3,4-dihydroxy-2h-furan-5-one;hydrate Chemical compound O.OC[C@H](O)[C@H]1OC(=O)C(O)=C1O FXXMDJFRMDVSCF-RXSVEWSESA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241000195940 Bryophyta Species 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical group [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RKWGIWYCVPQPMF-UHFFFAOYSA-N Chloropropamide Chemical compound CCCNC(=O)NS(=O)(=O)C1=CC=C(Cl)C=C1 RKWGIWYCVPQPMF-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000000232 Lipid Bilayer Substances 0.000 description 1
- 229920000433 Lyocell Polymers 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical class C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000004665 cationic fabric softener Substances 0.000 description 1
- 239000002752 cationic softener Substances 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 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
- 229940125773 compound 10 Drugs 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000004855 creaseproofing Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- OGQYPPBGSLZBEG-UHFFFAOYSA-N dimethyl(dioctadecyl)azanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC OGQYPPBGSLZBEG-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
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- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- AIRPJJGSWHWBKS-UHFFFAOYSA-N hydroxymethylphosphanium;chloride Chemical compound [Cl-].OC[PH3+] AIRPJJGSWHWBKS-UHFFFAOYSA-N 0.000 description 1
- 150000002462 imidazolines Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
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- 239000007788 liquid Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000011929 mousse Nutrition 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000004669 nonionic softener Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000006179 pH buffering agent Substances 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 229940055076 parasympathomimetics choline ester Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920006294 polydialkylsiloxane Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 229910021647 smectite Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 229910001388 sodium aluminate Inorganic materials 0.000 description 1
- 239000000429 sodium aluminium silicate Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- SONHXMAHPHADTF-UHFFFAOYSA-M sodium;2-methylprop-2-enoate Chemical compound [Na+].CC(=C)C([O-])=O SONHXMAHPHADTF-UHFFFAOYSA-M 0.000 description 1
- XFTALRAZSCGSKN-UHFFFAOYSA-M sodium;4-ethenylbenzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=C(C=C)C=C1 XFTALRAZSCGSKN-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/10—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing oxygen
- D06M13/184—Carboxylic acids; Anhydrides, halides or salts thereof
- D06M13/207—Substituted carboxylic acids, e.g. by hydroxy or keto groups; Anhydrides, halides or salts thereof
-
- 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
- D06M14/00—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials
- D06M14/02—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin
- D06M14/04—Graft polymerisation of monomers containing carbon-to-carbon unsaturated bonds on to fibres, threads, yarns, fabrics, or fibrous goods made from such materials on to materials of natural origin of vegetal origin, e.g. cellulose or derivatives thereof
-
- 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
- D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
-
- 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
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile
-
- 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
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/02—Natural fibres, other than mineral fibres
- D06M2101/04—Vegetal fibres
- D06M2101/06—Vegetal fibres cellulosic
-
- 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
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/20—Treatment influencing the crease behaviour, the wrinkle resistance, the crease recovery or the ironing ease
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
A method of treating fabric comprises wetting the fabric and drying the wet fabric in a domestic tumble dryer in the presence of a composition comprising a polymerisable monomer which forms a cross-linked polymer network on the fabric during drying.
Description
C4058 (C) 2366568 METHOD OF TREATING FABRIC
Technical Field
5 This invention relates to a method of treating a fabric, in particular a method of treating a fabric during drying. The invention also relates to a fabric care composition and to the use of the composition in the treatment of fabric.
10 Background and Prior Art
The creasing of fabrics is an almost inevitable consequence of cleaning fabrics, such as in a domestic laundering process. Fabrics also become creased in wear. Creasing can 15 be a particular problem for fabrics which contain cellulosic fibres such as cotton because the creasing is often difficult to remove. Generally, the creases which are developed in a fabric during laundering are removed by ironing. However, because ironing is seen as a time 20 consuming chore, there is an increasing trend for fabrics to be designed such that the need for ironing is reduced or eliminated altogether and/or the effort required for ironing is lower.
25 Methods of drying wet fabric can cause the fabric to become creased. For example, when fabrics (such as cotton fabrics) are dried in a conventional, domestic tumble dryer, the resulting dry fabric is generally creased to some extent.
30 Compositions for reducing the wrinkling of fabric are described in WO 96/15309 and Wo 96/15310. The compositions C4058 (C) contain a silicone and a film-forming polymer and it appears that it is the lubricating effect of the silicone which is responsible for their anti-wrinkle properties. This conclusion is supported by the fact that a wide variety of
5 polymers is mentioned as being suitable for use in the compositions.
Industrial treatments of fabrics, using pre-formed polymers, to reduce their tendency to crease are known. JP-A-04-50234 10 describes a textile treatment in which the crease resistance of a plain weave cotton fabric is increased by applying a so-called "shape memory resin" to the fabric. However, this document teaches that the resin is applied to the fabric at a relatively high amount of 10% by weight on weight of 15 fabric and it is not clear how this level of resin affects other properties of the fabric.
A relationship between polymer elastic properties and the ability to impart improved wrinkle recovery to cotton fabric 20 is described by Rawls et al in Journal of Applied Polymer Science, vol. 15, pages 341-349 (1971). A variety of different pre-formed polymeric elastomers was applied to fabric and, particularly in the few cases where thermoplastic elastomers were used, the polymers were 25 applied to the fabric at the relatively high levels of 4% and above.
The treatment of fabrics with cross-linking agents in order to impart antiwrinkle properties is known. Compounds such 30 as formaldehyde-based polymers, DMDHEU (dimethylol dihydroxy ethylene urea) and BTCA (butyl-1,2,3,4-tetracarboxylic acid) C4058 (C) may be used as the cross-linking agent. However, these treatments have the disadvantage of reducing the tensile strength of the fabrics.
5 The grafting of polymers of hydrophilic monomers onto cellulose is described in EP-A-0811718. The treatment of woven or knitted cellulosic fabrics occurs at a high temperature of 80C to 200C in this industrial process.
10 US 5204175 describes the production of a water absorptive fabric by heating fabric impregnated with a polymerisable monomer and a cross-linking agent in the presence of a water soluble resin.
15 Industrial treatments of fabric to impart permanent creases or to improve wet crease recovery are disclosed in US 3434161 and US 3505002, US 3434161 involves the polymerisation of vinyl groups, previously bound to the cellulose of the fabric, using high energy ionising 20 radiation. US 505002 describes the formation of polymers on textiles by reacting a nitrogenous product with formaldehyde.
Graft polymerisation of acrylamide onto cotton in industrial 25 textile treatments is described in Ghosh et al, Journal of Applied Polymer Science, Vol. 58, 1727-1734 (1995) and Hebeish et al, American Dyestuff Reporter, September 1983, 48-64.
C4058 (C) Grafting of acrylic acid onto cotton fabric is disclosed in Hebeish et al, Journal of Applied Polymer Science, Vol. 60, 2165-2176 (1996).
5 Bhat et al, Textile Res. J, 69 (1) 38-42 (1999) relates to plasma grafted cotton and polyester fabrics.
The production of crease-resistant cottons by polymerising N-methylol acrylamide onto fabric is disclosed in Moncrieff, The Textile Manufacturer, June, 1967, 233-235.
Warburton, Textile Research Journal, January, 1970, 68-74 describes creaseproofing cotton by in situ polymerisation of N-methylol acrylamide, acrylamide and tetrakis 15 (hydroxymethyl) phosphonium chloride.
All of the fabric treatments mentioned above are applied to the fabric on an industrial scale, before the fabric has been made up into a finished article (such as a garment).
20 The treatments are generally carried out in ovens at a high temperature.
The present invention aims to provide an alternative method for reducing the creasing of fabrics which can be applied 25 domestically (ie, in a domestic environment rather than industrially). In particular, the present invention aims to reduce the creasing of fabrics which occurs during drying of the wet fabric in domestic tumble dryers.
30 Definition of the Invention C4058 (C) Accordingly, the present invention provides a method of treating a fabric which comprises wetting the fabric and drying the wet fabric in a tumble dryer in the presence of a composition comprising a polymerisable monomer which forms a 5 cross-linked polymer on the fabric during drying.
Also provided by the invention is a fabric care composition comprising a textile compatible carrier and a polymerisable monomer which is capable of forming a cross-linked polymer 10 on a fabric during drying of the fabric.
The invention further provides the use of the composition of the invention in the treatment of a fabric as part of a laundering process.
Detailed Description of the Invention
The present invention involves the formation of a crosslinked polymer on the fabric during drying of the fabric.
20 It will be appreciated that the term "formation of a crosslinked polymer on the fabric" encompasses the formation of a network on and/or in the fibres of the fabric including physical and/or chemical attachment (eg, by grafting onto the polymer).
The method of the invention involves wetting the fabric. The term "wetting", as used herein, means increasing the level of water of part or all of the fabric above the normal level of water which is present in the fabric at the ambient 30 temperature, pressure and humidity. Therefore, when wet, all or part of the fabric (preferably all of the fabric) C4058 (C) will be saturated with water. The fabric can be wet as a result of a prior treatment, such as, for example, washing and rinsing in a laundering process. Alternatively, the fabric may be wet for other reasons. For example, the 5 composition which comprises the polymerisable monomer may be (and preferably is) aqueous and the wetting of the fabric may therefore be caused solely or partly by application of the composition to the fabric, eg, by soaking the fabric in the composition or spraying the composition onto the fabric.
The composition which is used in the method of the invention comprises a polymerisable monomer. Any monomer which is capable of polymerising on wet fabric during drying of the 15 fabric can, in principle, be used. The monomer may be polymerisable by free radical, anionic or cationic mechanisms or by a combination of one or more of these mechanisms. The monomer preferably has a molecular weight of 500 daltons or less, more preferably 200 daltons or less.
20 Advantageously, the monomer is water soluble in order that it can be readily taken up onto wet fabric and/or incorporated into an aqueous composition for application to the fabric.
25 The monomer preferably comprises one or more carbon-carbon double bonds, more preferably one carbon-carbon double bond, through which the polymerisation of the monomer can take place. Suitable groups which provide a polymerisable carbon-carbon double bond include acrylate esters, 30 acrylamides, acrylic acids or their salts, methacrylate esters, methacrylamides, methacrylic acids or their salts, C4058 (C) vinyl esters, vinyl ethers, sulphonated styrenes and salts thereof and vinyl pyrrolidones. The esters may contain functional groups in the alcohol residue, such as hydroxyl or amino. The monomer may contain functional or non- 5 functional groups other than those which provide the carboncarbon double bond(s).
Desirably, the monomer is non-toxic. Preferred monomers include those containing an acrylic acid group, a 10 methacrylic acid group (or a salt of an acrylic or methacrylic acid group such as a sodium salt), an acrylate ester or methyacrylate ester group or an acrylamide or methacrylamide group. Acrylate and methacrylate esters include esters of C, to C6 straight chain or branched, 15 aliphatic or alicyclic alcohols, preferably di- or polyhydroxylated alcohols (which are more water soluble than the unhydroxylated alcohols).
The invention results in the formation of a cross-linked 20 polymer network on the fabric. The cross-linking of the polymer may be an inherent consequence of the polymerisation of the monomer; for example, the monomer may contain two or more polymerisable groups. Alternatively, a cross-linking agent may be included in the composition in order to form 25 the cross-linked polymer. For example, when the monomer contains one polymerisable group and, when polymerised by itself, would not form a cross-linked polymer, a crosslinking agent containing two or more of the same or different polymerisable groups may be included in the 30 composition to ensure that a cross-linked polymer is formed on the fabric. Therefore, preferred cross-linking agents C4058 (C) include those comprising two or more carbon-carbon double bonds. The carbon-carbon double bonds are preferably provided by the same groups as in the polymerisable monomer. The cross-linking agent, when present in the composition for 5 use in the method of the invention, is preferably used in an amount of from 0.1 to 15% by weight, preferably 0.5 to 10% by weight, based on the weight of the polymerisable monomer.
10 The composition for use in the method of the invention may contain other components besides the polymerisable monomer and the optional crosslinking agent. For example, the composition may comprise one or more additional polymerisable monomers or cross-linking agents, one or more 15 vehicles or carriers for the composition, an initiator system for the polymerisation reaction and, optionally, stabilisers. Furthermore, when the composition for use in the method of the invention is a fabric care composition of the invention, it may contain further components, as 20 described hereinbelow.
Vehicles or carriers for the composition include water. Therefore, the composition is preferably aqueous, more preferably an aqueous solution, suspension or dispersion.
25 The composition preferably contains more than 50% by weight of water.
Initiator systems may be included in the compositions for use in the method of the invention. Initiator systems may 30 not be required if the monomer polymerises in air and/or light at the temperature at which the fabric is dried.
C4058 (C) However, the use of initiator systems is required or is desirable when polymerisation of the monomer does not occur or occurs in an unpredictable manner during drying of the fabric under normal conditions (eg, in the presence of air 5 and light at a temperature of 30'C to 80'C). The initiator system may cause the polymerisation to occur by free radical, anionic or cationic routes. Suitable radical, anionic and cationic initiators are well-known to those skilled in the art. A particularly preferred initiator 10 system for use with monomers containing acrylate, methacrylate, acrylic acid (or salts thereof), methacrylic acid (or salts thereof), acrylamide or methacrylamide groups comprises hydrogen peroxide and ascorbic acid. When hydrogen peroxide and ascorbic acid are used as the 15 initiator, they are preferably used in an amount of up to 10% (more preferably 0.1 to 5%) by weight based on total weight of polymerisable monomer.
The composition is applied to the fabric in an amount such 20 that creasing of the fabric is reduced (relative to fabric not treated with the composition) by the formation of the cross-linked polymer on the fabric. Preferably, the composition is applied to the fabric in an amount such that the amount of polymerisable monomer is from 0.1 to 10% by 25 weight on weight of fabric (owf), more preferably 0.1 to 5% owf. The amount of the cross-linked polymer formed on the fabric is preferably from 0.1 to 10% by weight on weight of fabric (owf), more preferably from 0.1 to 6% owf.
30 The method of the invention is preferably carried out as part of a laundering process. Laundering processes include C4058 (C) large scale and small scale (eg, domestic) laundering of fabric. The method of the invention can be part of a conventional laundering process. Thus, the composition which is used in the method of the invention may be a fabric 5 care composition of the invention, as described hereinbelow, and may be used at any convenient stage of a laundering process, for example when the fabric is already wet after a washing or rinsing step. The composition may therefore be in the form of a rinse adjunct or a fabric softening and/or 10 conditioning composition. Alternatively, the method of the invention may be carried out as a separate step either as part of, or independently from, the laundering process. Suitable product forms therefore also include products suitable for use in a method which involves soaking the wet 15 or dry fabric in a solution of the composition and/or spraying the composition onto wet or dry fabric.
Drying of the fabric is carried out in a tumble dryer. The temperature in the tumble dryer may vary from 400C to 800C.
20 The formation of a cross-linked polymer network on the fabric preferably takes place from 1 to 15 minutes (more preferably 2 to 15 minutes) after the start of the drying process. In the first minute or so of drying wet fabric in a tumble dryer, creases formed in the wet fabric tend to be 25 dissipated. After 15 minutes of drying in a tumble dryer, creases can become strongly formed in the fabric on account of the low moisture content of the fabric.
The term "tumble dryer", as used herein, covers any device 30 for drying wet fabric which causes the fabric to move, under the influence of gravity, through air at an elevated C4058 (C) temperature within a container (eg, a drum), preferably by rotation of part of the device (eg, the drum). Preferably, the tumble dryer is adapted for domestic use, rather than industrial or other large scale use. 5 The fabrics which may be treated in the present invention may be synthetic or may comprise cellulosic fibres, preferably from 1% to 100% cellulosic fibres (more preferably 5% to 100% cellulosic fibres, most preferably 40% 10 to 100%). When the fabric contains less than 100% cellulosic fibres, the balance comprises other fibres or blends of fibres suitable for use in garments such as synthetic fibres, eg polyester, for example. Preferably, the cellulosic fibres are of cotton or regenerated cellulose 15 such as Viscose (TM), Tencel (TM) or Modal (TM). The fabrics may be in the form of one or more garments.
The composition which may be used in the method of the invention may be a fabric care composition of the invention.
The fabric care composition of the invention comprises a textile compatible carrier.
The nature of the textile compatible carrier will be 25 dictated to a large extent by the stage at which the composition of the invention is used in a laundering process, the compositions being capable of being used, in principle, at any stage of the process. For example, where the compositions are for use as main wash detergent 30 compositions, the one or more textile compatible carriers comprise a detergent active compound. Where the C4058 (C) compositions are for use in the rinsing step of a laundering process, the one or more textile compatible carriers may comprise a fabric softening and/or conditioning compound.
5 The compositions of the invention preferably comprise a perfume, such as of the type which is conventionally used in fabric care compositions. The compositions may be packaged and labelled for use in a domestic laundering process.
10 Preferably, the fabric care composition is used to treat the fabric in the rinse cycle of a laundering process. The rinse cycle preferably follows the treatment of the fabric with a detergent composition.
15 Detergent Active Compounds If the fabric care composition of the present invention is in the form of a detergent composition, the textilecompatible carrier may be chosen from soap and non-soap 20 anionic, cationic, nonionic, amphoteric and zwitterionic detergent active compounds, and mixtures thereof.
Many suitable detergent active compounds are available and are fully described in the literature, for example, in 25 "Surface-Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
The preferred textile-compatible carriers that can be used are soaps and synthetic non-soap anionic and nonionic 30 compounds.
C4058 (C) Anionic surfactants are well-known to those skilled in the art. Examples include alkylbenzene sulphonates, particularly linear alkylbenzene sulphonates having an alkyl chain length Of C8_C15; primary and secondary alkylsulphates, 5 particularly C8-Cj5 primary alkyl sulphates; alkyl ether sulphates; olefin sulphonates; alkyl xylene sulphonates; dialkyl sulphosuccinates; and fatty acid ester sulphonates. Sodium salts are generally preferred.
10 Nonionic surfactants that may be used include the primary and secondary alcohol ethoxylates, especially the C8-C20 aliphatic alcohols ethoxylated with an average of from 1 to 20 moles of ethylene oxide per mole of alcohol, and more especially the C10-C15 primary and secondary aliphatic 15 alcohols ethoxylated with an average of from 1 to 10 moles of ethylene oxide per mole of alcohol. Non-ethoxylated nonionic surfactants include alkylpolyglycosides, glycerol monoethers, and polyhydroxyamides (glucamide).
20 Cationic surfactants that may be used include quaternary ammonium salts of the general formula RlR2R3R4N+ X_ wherein the R groups are independently hydrocarbyl chains of Cl-C22 length, typically alkyl, hydroxyalkyl or ethoxylated alkyl groups, and X is a solubilising cation (for example, 25 compounds in which R, is a CB-C22 alkyl group, preferably a C8-Clo or C12_C14 alkyl group, R2 is a methyl group, and R3 and R4, which may be the same or different, are methyl or hydroxyethyl groups); and cationic esters (for example, choline esters) and pyridinium salts.
C4058 (C) The total quantity of detergent surfactant in the composition is suitably from 0.1 to 60 wt% e.g. 0.5-55 wt%, such as 5-50wt%.
5 Preferably, the quantity of anionic surfactant (when present) is in the range of from 1 to 50% by weight of the total composition. More preferably, the quantity of anionic surfactant. is in the range of from 3 to 35% by weight, e.g. 5 to 30% by weight.
Preferably, the quantity of nonionic surfactant when present is in the range of from 2 to 25% by weight, more preferably from 5 to 20% by weight.
15 Amphoteric surfactants may also be used, for example amine oxides or betaines.
The compositions may suitably contain from 10 to 70%, preferably from 15 to 70% by weight, of detergency builder.
20 Preferably, the quantity of builder is in the range of from 15 to 50% by weight.
The detergent composition may contain as builder a crystalline aluminosilicate, preferably an alkali metal 25 aluminosilicate, more preferably a sodium aluminosilicate.
The aluminosilicate may generally be incorporated in amounts of from 10 to 70% by weight (anhydrous basis), preferably from 25 to 50%. Aluminosilicates are materials having the 30 general formula:
C4058 (C) 0.8-1.5 M20- A1203 0.8-6 Si02 where M is a monovalent cation, preferably sodium. These materials contain some bound water and are required to have 5 a calcium ion exchange capacity of at least 50 mg CaO/g. The preferred sodium aluminosilicates contain 1.5-3.5 Si02 units in the formula above. They can be prepared readily by reaction between sodium silicate and sodium aluminate, as amply described in the literature.
Fabric Softening and/or Conditioner Compounds If the composition of the present invention is in the form of a fabric conditioner composition, the textile-compatible 15 carrier will be a fabric softening and/or conditioning compound (hereinafter referred to as "fabric softening compound"), which may be a cationic or nonionic compound.
The softening and/or conditioning compounds may be water 20 insoluble quaternary ammonium compounds. The compounds may be present in amounts of up to 8% by weight (based on the total amount of the composition) in which case the compositions are considered dilute, or at levels from 8% to about 50% by weight, in which case the compositions are 25 considered concentrates.
Compositions suitable for delivery during the rinse cycle may also be delivered to the fabric in the tumble dryer if used in a suitable form. Thus, another product form is a 30 composition (for example, a paste) suitable for coating onto, and delivery from, a substrate e.g. a flexible sheet C4058 (C) or sponge or a suitable dispenser during a tumble dryer cycle.
Suitable cationic fabric softening compounds are 5 substantially water-insoluble quaternary ammonium materials comprising a single alkyl or alkenyl long chain having an average chain length greater than or equal to C20 or, more preferably, compounds comprising a polar head group and two alkyl or alkenyl chains having an average chain length 10 greater than or equal to C14- Preferably the fabric softening compounds have two long chain alkyl or alkenyl chains each having an average chain length greater than or equal to C16- Most preferably at least 50% of the long chain alkyl or alkenyl groups have a chain length of C18 or above.
15 It is preferred if the long chain alkyl or alkenyl groups of the fabric softening compound are predominantly linear.
Quaternary ammonium compounds having two long-chain aliphatic groups, for example, distearyldimethyl ammonium 20 chloride and di(hardened tallow alkyl) dimethyl ammonium chloride, are widely used in commercially available rinse conditioner compositions. Other examples of these cationic compounds are to be found in "Surface- Active Agents and Detergents", Volumes I and II, by Schwartz, Perry and Berch.
25 Any of the conventional types of such compounds may be used in the compositions of the present invention.
The fabric softening compounds are preferably compounds that provide excellent softening, and are characterised by a 30 chain melting LP to La transition temperature greater than 250C, preferably greater than 350C, most preferably greater C4058 (C) than 450C. This LO to La transition can be measured by DSC as defined in "Handbook of Lipid Bilayers", D Marsh, CRC Press, Boca Raton, Florida, 1990 (pages 137 and 337). Substantially water-insoluble fabric softening compounds are 5 defined as fabric softening compounds having a solubility of less than 1 x 10-3 Wt % in demineralised water at 20'C. Preferably the fabric softening compounds have a solubility of less than 1 X 10-4 Wt%, more preferably less than 1 x 10-8 to 1 X 10-6 Wt%.
Especially preferred are cationic fabric softening compounds that are water-insoluble quaternary ammonium materials having two C12-22 alkyl or alkenyl groups connected to the molecule via at least one ester link, preferably two ester 15 links. An especially preferred ester-linked quaternary ammonium material can be represented by the formula II:
Ri R3-T-R2 (II) (CH2) P_T-R2 wherein each R, group is independently selected f rom C1-4 30 alkyl or hydroxyalkyl groups or C2-4 alkenyl groups; each R2 group is independently selected from CS-28 alkyl or alkenyl groups; and wherein R3 is a linear or branched alkylene group of 1 to 5 carbon atoms, T is C4058 (C) 0 0 11 11 and p is 0 or is an integer from 1 to 5.
Di(tallowoxyloxyethyl) dimethyl ammonium chloride and/or its hardened tallow analogue is especially preferred of the 10 compounds of formula (II).
A second preferred type of quaternary ammonium material can be represented by the formula (III):
15 OOCR2 (RI) 3N± (CH2) p H (III) 1 C;H200CR2 wherein R1, p and R2 are as def ined above.
25 It is advantageous if the quaternary ammonium material is biologically biodegradable.
Preferred materials of this class such as 1,2-bis(hardened tallowoyloxy)-3-trimethylammonium propane chloride and their 30 methods of preparation are, for example, described in US 4 137 180 (Lever Brothers Co). Preferably these materials comprise small amounts of the corresponding monoester as described in US 4 137 180, for example, 1-hardened tallowoyloxy-2-hydroxy-3-trimethylammonium 35 propane chloride.
C4058 (C) Other useful cationic softening agents are alkyl pyridinium salts and substituted imidazoline species. Also useful are primary, secondary and tertiary amines and the condensation products of fatty acids with alkylpolyamines. 5 The compositions may alternatively or additionally contain water-soluble cationic fabric softeners, as described in GB 2 039 556B (Unilever).
10 The compositions may comprise a cationic fabric softening compound and an oil, for example as disclosed in EP-A0829531.
The compositions may alternatively or additionally contain 15 nonionic fabric softening agents such as lanolin and derivatives thereof.
Lecithins are 'also suitable softening compounds.
20 Nonionic softeners include LP phase forming sugar esters (as described in M Hato et al Langmuir 12, 1659, 1666, (1996)) and related materials such as glycerol monostearate or sorbitan esters. Often these materials are used in conjunction with cationic materials to assist deposition 25 (see, for example, GB 2 202 244). Silicones are used in a similar way as a co-softener with a cationic softener in rinse treatments (see, for example, GB 1 549 180).
The compositions may also suitably contain a nonionic 30 stabilising agent. Suitable nonionic stabilising agents are C4058 (C) linear C8 to C22 alcohols alkoxylated with 10 to 20 moles of alkylene oxide, C10 to C20 alcohols, or mixtures thereof.
Advantageously the nonionic stabilising agent is a linear C8 5 to C22 alcohol alkoxylated with 10 to 20 moles of alkylene oxide. Preferably, the level of nonionic stabiliser is within the range from 0.1 to 10% by weight, more preferably from 0.5 to 5% by weight, most preferably from 1 to 4% by weight. The mole ratio of the quaternary ammonium compound 10 and/or other cationic softening agent to the nonionic stabilising agent is suitably within the range from 40:1 to about 1:1, preferably within the range from 18:1 to about 3:1.
15 The composition can also contain fatty acids, for example C8 to C24 alkyl or alkenyl monocarboxylic acids or polymers thereof. Preferably saturated fatty acids are used, in particular, hardened tallow Cjr, to Cjs fatty acids. Preferably the fatty acid is non-saponified, more preferably 20 the fatty acid is free, for example oleic acid, lauric acid or tallow fatty acid. The level of fatty acid material is preferably more than 0.1% by weight, more preferably more than 0.2% by weight. Concentrated compositions may comprise from 0.5 to 20% by weight of fatty acid, more preferably 1% 25 to 10% by weight. The weight ratio of quaternary ammonium material or other cationic softening agent to fatty acid material is preferably from 10:1 to 1:10.
The fabric conditioning compositions may include silicones, 30 such as predominately linear polydialkylsiloxanes, e.g. polydimethylsiloxanes oraminosilicones containing amine- C4058 (C) functionalised side chains; soil release polymers such as block copolymers of polyethylene oxide and terephthalate; amphoteric surfactants; smectite type inorganic clays; zwitterionic quaternary ammonium compounds; and nonionic 5 surfactants.
The fabric conditioning compositions may also include an agent which produces a pearlescent appearance, e.g. an organic pearlising compound such as ethylene glycol 10 distearate, or inorganic pearlising pigments such as microfine mica or titanium dioxide (Ti02) coated mica.
The fabric conditioning compositions may be in the form of emulsions or emulsion precursors thereof.
Other optional ingredients include emulsifiers, electrolytes (for example, sodium chloride or calcium chloride) preferably in the range from 0.01 to 5% by weight, pH buffering agents, and perfumes (preferably from 0.1 to 5% by 20 weight).
Further optional ingredients include non-aqueous solvents, perfume carriers, fluorescers, colourants, hydrotropes, antifoaming agents, antiredeposition agents, enzymes, 25 optical brightening agents, opacifiers, dye transfer inhibitors, anti- shrinking agents, anti-wrinkle agents, anti-spotting agents, germicides, fungicides, anti-oxidants, UV absorbers (sunscreens), heavy metal sequestrants, chlorine scavengers, dye fixatives, anti-corrosion agents, 30 drape imparting agents, antistatic agents and ironing aids. This list is not intended to be exhaustive.
C4058 (C) Fabric Treatment Products The composition of the invention may be in the form of a 5 liquid, solid (e.g. powder or tablet), a gel or paste, spray, stick or a foam or mousse. Examples including a soaking product, a rinse treatment (e.g. conditioner or finisher) or a mainwash product. The composition may also be applied to a substrate e.g. a flexible sheet or used in a 10 dispenser which can be used in the wash cycle, rinse cycle or during the dryer cycle.
The invention will now be described by way of example only and with reference to the following non-limiting examples.
EXAMPLES
Experimental method:
20 Cotton sheeting was used for all testing and ballast. This was prewashed with Persil Non-Biological (trade mark) washing powder (100g Persil per 2.5 kg load) at 400C cotton setting (C) in a Zanussi Jetstream (trade mark) machine. Cotton sheet sample size was 30 cm x 20 cm.
Solutions were made up by mixing the appropriate amounts of acrylamide, methylene bisacrylamide, hydrogen peroxide solution, ascorbic acid and demineralised water.
C4058 (C) - 23 These solutions were then immediately padded onto the dry ("'flat") cotton samples using a Mathis Padder (pressure-60, 2.5m/min), giving approximately 100% solution pick up.
5 After padding, the samples were immediately tumble dried for 20 minutes at the high temperature cotton setting using a Zanussi TD 525 (trade mark) European-style tumble dryer.
The samples were then removed and assessed for creasing 10 intensity against AATCC Wrinkle Recovery (1-5) standards (1 = highly creased, 5 = very flat and intermediate numbers are between these levels of creasing). Each score is the average of three replicates.
C4058 (C) Example Solution Components (% Polym %Xlink AATCC W/W) % Score Am BAm HPO AA Wate r 1 0 0 0 0 100 0 - 2 2 0.4 0.01 0.02 0.00 99.5 0.5 3 2.5 3 85 5 7 75 98.9 1 3 3.4 4 0.9 0.03 0.05 0.01 96.8 3 3 3.1 5 70 0 5 5 94.7 5 3 3.5 6 2.9 0.09 0.16 0.04 92.5 7 3 3.7 7 10 0 4 5 89.3 10 3 4.3 8 4.8 0.15 0.27 0.07 94.7 5 0 2.4 9 50 0 3 5 94.7 5 0.5 2.7 10 6.7 0.21 0.38 0.10 94.7 5 1 3.8 11 90 0 2 5 94.7 5 5 3.3 12 9.7 0.30 0.54 0.15 94.7 5 10 3.8 00 0 5 0 5.0 0 0.27 0.07 00 0.02 3 5 4.9 5 0.27 0.07 75 0.05 3 5 4.9 0 0.27 0.07 50 0.25 3 5 4.7 0 0.27 0.07 50 0.50 3 5 4.5 0 0.27 0.07 00 3 5 Am=acrylamide BAm=methylene bisacrylamide HPO=hydrogen peroxide solution (27.5% active) C4058 (C) AA=ascorbic acid Water=demineralised water % by weight of polymer on the fabric (owf) 5 % by weight of cross-linker in the solution based on weight of monomer Am Thus, in all of Examples 1 to 12, the creasing of the fabri was reduced.
EXAMPLES 13 TO 20 Example 5 was repeated using a variety of different monomers. Treated fabrics were dried in a Miele Novotronic 15 T430 (trade mark) tumble dryer. The results are set out in the following table.
Example Solution Components (% w/w) %Polym %XlInk AATCC Monomer Mon. Wt Xlinker Xlink. HPO AA APS Score Wt. WR 1-E 13 SA 4.85 EGDMA 0.15 0.27 0.075 5 3 2.6 14 SA 4.85 BAm 0.15 0.27 0.075 5 3 2.8 15 SMA 4.85 BAm 0.15 0.27 0.075 5 3 3.7 16 HEA 4.85 BAm 0.15 0.27 0.075 5 3 3.6 17 HEMA 4.85 BAm 0.15 0.27 0.075 5 3 3.7 18 SSASS 4.85 BAm 0.15 0.27 0.075 5 3 2.9 19 DMAEA 4.85 BAm 0.15 0.27 0.075 5 3 3.8 20 DMAEA 4.85 BAm 0.15 0.075 5 3 3.5 C4058 (C) SA Sodium acrylate SMA Sodium methacrylate HEA 2-Hydroxy ethyl acrylate HEMA 2-Hydroxy ethyl methacrylate DMAEA N,N-dimethyl amino ethyl acrylate SSASS 4-Styrene sulfonic acid, sodium salt EGDMA Ethylene glycol dimethacrylate APS Ammonium persulfate EXAMPLES 21 To 23 The following rinse conditioner formulations were prepared.
SMA - Sodium Methacrylate 10 BAM - Methylene Bis-Acrylamide HPO - Hydrogen Peroxide (27.5% Active) AA - Ascorbic Acid DW - Deionised Water Supplied by Lever Brothers, UK (Comfort is a trade mark) - 15 a standard rinse conditioner Example SMA BAM HPO AA Comfort DW Concentrate 1 4.85 0.15 0.27 0.07 1.5 93.155 2 4.85 0.15 0.27 0.07 37.0 57.655 3 4.85 0.15 0.27 0.07 74.1 20.555 C4058 (C)
Claims (18)
1. Method of treating a fabric which comprises wetting the fabric and drying the wet fabric in a tumble dryer in the 5 presence of a composition comprising a polymerisable monomer which forms a cross-linked polymer on the fabric during drying.
2. Method as claimed in Claim 1, wherein the polymerisable 10 monomer comprises a carbon-carbon double bond provided by a group selected from acrylate esters, acrylamides, acrylic acids or their salts, methacrylate esters, methacrylamides, methacrylic acids or their salts, vinyl esters, vinyl ethers, sulphonated styrenes and salts thereof and vinyl 15 pyrrolidones.
3. Method as claimed in Claim 1 or Claim 2, wherein the polymerisable monomer comprises an acrylic acid or acrylic salt group, an acrylate ester group or an acrylamide group.
4. Method as claimed in any one of Claims 1 to 3, wherein the polymerisable monomer is water soluble.
5. Method as claimed in any one of Claims 1 to 4, wherein 25 the composition is a mixture of a polymerisable monomer and a cross- linking agent.
6. Method as claimed in any one of Claims I to 5, wherein the composition comprises an initiator for the 30 polymerisation reaction of the monomer.
C4058 (C)
7. Method as claimed in Claim 6, wherein the initiator comprises hydrogen peroxide and ascorbic acid.
8. Method as claimed in any one of Claim 1 to 8, wherein the drying is carried out at a temperature of from 400C to 800C.
9. Method as claimed in any one of Claims 1 to 9, wherein the cross-linked polymer is formed from 1 to 15 minutes 10 after the start of the drying process.
10. Method as claimed in any one of Claims 1 to 9, wherein the cross-linked polymer which is formed on the fabric is present in an amount of from 0.1 to 10% by weight on weight 15 of fabric.
11. Method as claimed in any one of Claims 1 to 10, wherein the composition is applied to the fabric by spraying.
20
12. Method as claimed in any one of Claims 1 to 11 which is part of a domestic laundering process.
13. Fabric care composition comprising a textile compatible carrier and a polymerisable monomer which is capable of 25 forming a cross-linked polymer on a fabric during drying of the fabric.
14. Composition as claimed in Claim 13 which further comprises a perfume.
C4058 (C)
15. Composition as claimed in Claim 13 or Claim 14 which is sprayable.
16. Composition as claimed in any one of Claims 13 to 15 5 which is a rinse adjunct or a fabric softening composition.
17. Composition as claimed in any one of Claims 13 to 16, wherein the composition or the one or more substances have the features of any one of Claims 2 to 7.
18. Use of a composition of any one of Claims 13 to 17 in the treatment of a fabric as part of a laundering process.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0021481A GB2366568A (en) | 2000-09-01 | 2000-09-01 | Method of treating fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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GB0021481A GB2366568A (en) | 2000-09-01 | 2000-09-01 | Method of treating fabric |
Publications (2)
Publication Number | Publication Date |
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GB0021481D0 GB0021481D0 (en) | 2000-10-18 |
GB2366568A true GB2366568A (en) | 2002-03-13 |
Family
ID=9898660
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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GB0021481A Withdrawn GB2366568A (en) | 2000-09-01 | 2000-09-01 | Method of treating fabric |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004039930A2 (en) * | 2002-10-30 | 2004-05-13 | Unilever Plc | Fabric care composition |
US7681328B2 (en) | 2002-04-22 | 2010-03-23 | The Procter & Gamble Company | Uniform delivery of compositions |
US8091253B2 (en) | 2004-08-26 | 2012-01-10 | The Procter & Gamble Company | Fabric article treating device and system |
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US4108748A (en) * | 1975-03-28 | 1978-08-22 | The United States Of America As Represented By The Secretary Of Agriculture | Photofinishing of cotton textiles |
GB2004899A (en) * | 1977-09-20 | 1979-04-11 | Kanebo Ltd | Method of treating synthetic fibres |
US4835020A (en) * | 1986-07-24 | 1989-05-30 | Mitsubishi Petrochemical Company Limited | Process for preparation of water absorptive composite material |
JPH01314782A (en) * | 1988-06-08 | 1989-12-19 | Tsutomu Kagitani | Modification of silk |
US5266632A (en) * | 1985-11-28 | 1993-11-30 | Institue Textile De France | Grafting reaction system and grafting process |
US5447537A (en) * | 1992-04-06 | 1995-09-05 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Cotton fabrics with improved strength retention |
EP0681053A1 (en) * | 1994-04-29 | 1995-11-08 | Nippon Sanmo Sensyoku Co.,Ltd. | Carboxyl group-modified cellulose or acryl fiber and process of producing same |
GB2295404A (en) * | 1994-10-21 | 1996-05-29 | Ici Plc | Creaseproofing treatment of fabrics |
-
2000
- 2000-09-01 GB GB0021481A patent/GB2366568A/en not_active Withdrawn
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4108748A (en) * | 1975-03-28 | 1978-08-22 | The United States Of America As Represented By The Secretary Of Agriculture | Photofinishing of cotton textiles |
GB2004899A (en) * | 1977-09-20 | 1979-04-11 | Kanebo Ltd | Method of treating synthetic fibres |
US5266632A (en) * | 1985-11-28 | 1993-11-30 | Institue Textile De France | Grafting reaction system and grafting process |
US4835020A (en) * | 1986-07-24 | 1989-05-30 | Mitsubishi Petrochemical Company Limited | Process for preparation of water absorptive composite material |
JPH01314782A (en) * | 1988-06-08 | 1989-12-19 | Tsutomu Kagitani | Modification of silk |
US5447537A (en) * | 1992-04-06 | 1995-09-05 | Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College | Cotton fabrics with improved strength retention |
EP0681053A1 (en) * | 1994-04-29 | 1995-11-08 | Nippon Sanmo Sensyoku Co.,Ltd. | Carboxyl group-modified cellulose or acryl fiber and process of producing same |
GB2295404A (en) * | 1994-10-21 | 1996-05-29 | Ici Plc | Creaseproofing treatment of fabrics |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7681328B2 (en) | 2002-04-22 | 2010-03-23 | The Procter & Gamble Company | Uniform delivery of compositions |
WO2004039930A2 (en) * | 2002-10-30 | 2004-05-13 | Unilever Plc | Fabric care composition |
WO2004039930A3 (en) * | 2002-10-30 | 2004-06-24 | Unilever Plc | Fabric care composition |
US8091253B2 (en) | 2004-08-26 | 2012-01-10 | The Procter & Gamble Company | Fabric article treating device and system |
Also Published As
Publication number | Publication date |
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GB0021481D0 (en) | 2000-10-18 |
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