US20020031970A1 - Methods for improving water absorbency of fabrics and fabrics with improved properties - Google Patents
Methods for improving water absorbency of fabrics and fabrics with improved properties Download PDFInfo
- Publication number
- US20020031970A1 US20020031970A1 US09/821,313 US82131301A US2002031970A1 US 20020031970 A1 US20020031970 A1 US 20020031970A1 US 82131301 A US82131301 A US 82131301A US 2002031970 A1 US2002031970 A1 US 2002031970A1
- Authority
- US
- United States
- Prior art keywords
- fabric
- formaldehyde
- fabrics
- water absorbency
- time
- 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
- 239000004744 fabric Substances 0.000 title claims abstract description 293
- 238000000034 method Methods 0.000 title claims abstract description 81
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims abstract description 68
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 267
- 239000000835 fiber Substances 0.000 claims abstract description 89
- 238000011282 treatment Methods 0.000 claims abstract description 59
- 239000000203 mixture Substances 0.000 claims abstract description 48
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 46
- 239000003054 catalyst Substances 0.000 claims abstract description 41
- 238000004132 cross linking Methods 0.000 claims abstract description 31
- 239000002243 precursor Substances 0.000 claims abstract description 29
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims abstract description 20
- 238000010438 heat treatment Methods 0.000 claims abstract description 11
- 230000000694 effects Effects 0.000 claims abstract description 9
- 229920000297 Rayon Polymers 0.000 claims description 69
- 239000002964 rayon Substances 0.000 claims description 50
- 229920005989 resin Polymers 0.000 claims description 41
- 239000011347 resin Substances 0.000 claims description 41
- 229920003180 amino resin Polymers 0.000 claims description 36
- 229920000742 Cotton Polymers 0.000 claims description 27
- 229920002678 cellulose Polymers 0.000 claims description 15
- 239000001913 cellulose Substances 0.000 claims description 15
- 230000001747 exhibiting effect Effects 0.000 claims description 5
- 239000000243 solution Substances 0.000 description 21
- 229920001296 polysiloxane Polymers 0.000 description 17
- 238000005406 washing Methods 0.000 description 17
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 16
- 229920000433 Lyocell Polymers 0.000 description 13
- 238000001723 curing Methods 0.000 description 13
- -1 i.e. Substances 0.000 description 13
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 12
- 238000004900 laundering Methods 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- 239000000080 wetting agent Substances 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 8
- 229910001629 magnesium chloride Inorganic materials 0.000 description 8
- 239000007864 aqueous solution Substances 0.000 description 7
- 229920002545 silicone oil Polymers 0.000 description 7
- 238000010998 test method Methods 0.000 description 7
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 239000004753 textile Substances 0.000 description 6
- 241000208202 Linaceae Species 0.000 description 5
- 235000004431 Linum usitatissimum Nutrition 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 239000000806 elastomer Substances 0.000 description 5
- 230000002209 hydrophobic effect Effects 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- WFDIJRYMOXRFFG-UHFFFAOYSA-N acetic acid anhydride Natural products CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 235000015165 citric acid Nutrition 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 229920002994 synthetic fiber Polymers 0.000 description 4
- 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 3
- 229920003043 Cellulose fiber Polymers 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- 239000012209 synthetic fiber Substances 0.000 description 3
- DETXZQGDWUJKMO-UHFFFAOYSA-N 2-hydroxymethanesulfonic acid Chemical compound OCS(O)(=O)=O DETXZQGDWUJKMO-UHFFFAOYSA-N 0.000 description 2
- WHBMMWSBFZVSSR-UHFFFAOYSA-N 3-hydroxybutyric acid Chemical compound CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000007844 bleaching agent Substances 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 235000004879 dioscorea Nutrition 0.000 description 2
- 150000004820 halides Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- YIXJRHPUWRPCBB-UHFFFAOYSA-N magnesium nitrate Chemical compound [Mg+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O YIXJRHPUWRPCBB-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- YNTOKMNHRPSGFU-UHFFFAOYSA-N n-Propyl carbamate Chemical compound CCCOC(N)=O YNTOKMNHRPSGFU-UHFFFAOYSA-N 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000003209 petroleum derivative Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 238000009999 singeing Methods 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 2
- GGAUUQHSCNMCAU-ZXZARUISSA-N (2s,3r)-butane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C[C@H](C(O)=O)[C@H](C(O)=O)CC(O)=O GGAUUQHSCNMCAU-ZXZARUISSA-N 0.000 description 1
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 description 1
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- XYOSFLPUWVWHOA-UHFFFAOYSA-N 2-ethylidenepropane-1,3-diol;urea Chemical compound NC(N)=O.CC=C(CO)CO XYOSFLPUWVWHOA-UHFFFAOYSA-N 0.000 description 1
- NNTWKXKLHMTGBU-UHFFFAOYSA-N 4,5-dihydroxyimidazolidin-2-one Chemical compound OC1NC(=O)NC1O NNTWKXKLHMTGBU-UHFFFAOYSA-N 0.000 description 1
- 244000303258 Annona diversifolia Species 0.000 description 1
- 235000002198 Annona diversifolia Nutrition 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- 241000282836 Camelus dromedarius Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 241000282852 Lama guanicoe Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241001494479 Pecora Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920002334 Spandex Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 241001416177 Vicugna pacos Species 0.000 description 1
- 241000282840 Vicugna vicugna Species 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical class CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- BIGPRXCJEDHCLP-UHFFFAOYSA-N ammonium bisulfate Chemical compound [NH4+].OS([O-])(=O)=O BIGPRXCJEDHCLP-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 210000000085 cashmere Anatomy 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000011284 combination treatment Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- STZIXLPVKZUAMV-UHFFFAOYSA-N cyclopentane-1,1,2,2-tetracarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC1(C(O)=O)C(O)=O STZIXLPVKZUAMV-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000009990 desizing Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 1
- 235000019838 diammonium phosphate Nutrition 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- WVJOGYWFVNTSAU-UHFFFAOYSA-N dimethylol ethylene urea Chemical compound OCN1CCN(CO)C1=O WVJOGYWFVNTSAU-UHFFFAOYSA-N 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-M ethanesulfonate Chemical compound CCS([O-])(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-M 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000675 fabric finishing Substances 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009962 finishing (textile) Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 238000005517 mercerization Methods 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- RMIODHQZRUFFFF-UHFFFAOYSA-N methoxyacetic acid Chemical compound COCC(O)=O RMIODHQZRUFFFF-UHFFFAOYSA-N 0.000 description 1
- SXVDZIOMWSPFCO-UHFFFAOYSA-N methyl n,n-bis(hydroxymethyl)carbamate Chemical compound COC(=O)N(CO)CO SXVDZIOMWSPFCO-UHFFFAOYSA-N 0.000 description 1
- 210000000050 mohair Anatomy 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- UFOIOXZLTXNHQH-UHFFFAOYSA-N oxolane-2,3,4,5-tetracarboxylic acid Chemical compound OC(=O)C1OC(C(O)=O)C(C(O)=O)C1C(O)=O UFOIOXZLTXNHQH-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 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
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- DSMDTSQLIDMSDR-UHFFFAOYSA-N propan-2-yl n,n-bis(hydroxymethyl)carbamate Chemical compound CC(C)OC(=O)N(CO)CO DSMDTSQLIDMSDR-UHFFFAOYSA-N 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000009738 saturating Methods 0.000 description 1
- 239000011492 sheep wool Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 239000004759 spandex Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical class OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 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
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
-
- 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
- D06M13/12—Aldehydes; Ketones
- D06M13/127—Mono-aldehydes, e.g. formaldehyde; Monoketones
-
- 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
- D06M15/693—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural or synthetic rubber, 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
- 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
- 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
- D06M2101/10—Animal fibres
- D06M2101/12—Keratin fibres or silk
-
- 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
-
- 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
-
- 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
- D06M2200/45—Shrinking resistance, anti-felting properties
-
- 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
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
-
- 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
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/603—Including strand or fiber material precoated with other than free metal or alloy
- Y10T442/607—Strand or fiber material is synthetic polymer
-
- 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
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/60—Nonwoven fabric [i.e., nonwoven strand or fiber material]
- Y10T442/696—Including strand or fiber material which is stated to have specific attributes [e.g., heat or fire resistance, chemical or solvent resistance, high absorption for aqueous compositions, water solubility, heat shrinkability, etc.]
Definitions
- This invention relates to methods for providing fabrics, particularly fabrics containing natural fibers such as cotton, rayon and the like, with good water absorbency in combination with durable press and/or shrinkage resistance.
- This invention also relates to cellulose fabrics which have improved water absorbency, particularly in combination with good durable press properties and/or shrinkage resistance.
- the formaldehyde release may occur not only throughout the preparation of the fabric but also during garment-making. Further, garments or fabrics treated with aminoplast resins may release additional formaldehyde when stored under humid conditions. Aminoplast resins may also hydrolyze during washing procedures, resulting in a loss of the durable press performance. Additionally, aminoplast resins tend to give fabric a harsher handle, that is, make the fabric feel less soft. As the resins make the fabric feel less soft, the fabric must be treated with additional softeners, for example silicone softeners. Unfortunately, the silicone softeners tend to make the fabric hydrophobic although it is often preferred that the fabric have hydrophilic properties.
- Cellulosic fibers have also been cross-linked with formaldehyde to impart durable press properties.
- the Payet U.S. Pat. Nos. 3,960,482, 3,960,483, 4,067,688 and 4,104,022 disclose durable press processes which comprise impregnating a cellulosic fiber-containing fabric with an aqueous solution comprising a catalyst, and, while the fabric has a moisture content of above 20% by weight, exposing the fabric to formaldehyde vapors and curing under conditions at which formaldehyde reacts with the cellulose.
- 4,108,598 discloses a process which comprises treating cellulosic fiber-containing fabrics with an aqueous solution of formaldehyde and a catalyst, heat curing the treated fabric by introducing the fabric into a heating zone, and gradually increasing the temperature of the heating zone, thereby increasing the temperature of the heated fabric to prevent the loss of an amount of formaldehyde which will reduce the overall extent of curing.
- the Payet U.S. Pat. No. 5,885,303 also discloses a durable press process for cellulosic fiber-containing fabrics.
- the process comprises treating the fabric with an aqueous solution of formaldehyde, a catalyst capable of catalyzing the cross-linking reaction between formaldehyde and cellulose, and an effective amount of a silicone elastomer to reduce loss in tear strength in the treated fabric.
- Formaldehyde is generally less expensive than aminoplast resins, and formaldehyde treatment of cellulosic fabrics typically results in durable press properties which are more durable than those obtained by aminoplast resins.
- the copending Payet application Ser. No. 09/163,319 discloses processes for providing rayon fabrics with durable press properties wherein a rayon fiber-containing fabric is treated with an aqueous mixture containing a high concentration of formaldehyde and a catalyst capable of catalyzing the cross-linking reaction between formaldehyde and the rayon, and the treated fabric is heat cured.
- the fabric may be washed or laundered in an aqueous system and does not shrink substantially on aqueous washing.
- a silicone elastomer may be employed to reduce loss in tear and tensile strength in the treated fabric.
- cellulose fabrics both cotton and rayon particularly, are naturally hydrophilic, and therefore absorb moisture.
- garments made of fabrics which are hydrophilic are more comfortable for wear and therefore are preferred by consumers over garments which are formed of hydrophobic, non-moisture absorbing fabrics.
- many conventional fabric treatments for improving durable press and/or for reducing shrinkage of cellulose fabrics, and particularly for cotton and rayon fabrics inhibit the natural water absorbency of the cellulose fibers and render the fabrics hydrophobic. Such fabrics are therefore not preferred for garment use owing to their reduced ability or substantial inability to absorb moisture.
- the invention is directed to methods for providing fabric with good water absorbency and durable press properties, which methods comprise treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde.
- the invention is directed to methods for providing fabric with good water absorbency and shrinkage resistance properties, which methods comprising treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde.
- the invention is directed to methods for providing rayon fabric with reduced shrinkage and good water absorbency, which methods comprise crosslinking cellulose in the fabric with formaldehyde and providing the fabric with a silicone elastomer.
- the invention is directed to fabric comprising rayon fibers and exhibiting a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time, and to fabric comprising cotton fibers and having a crosslinked formaldehyde durable press treatment and exhibiting a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time, wherein the fabric does not comprise 100% cotton.
- the methods of the invention are advantageous in providing fabrics which exhibit good water absorbency, particularly in combination with other desirable properties, for example durable press properties and/or shrinkage reduction.
- the present invention is directed to methods for providing fabrics, particularly fabrics comprising natural fibers, with good water absorbency in combination with good durable press properties and/or shrinkage resistance.
- This invention also relates to fabrics which have good water absorbency, particularly in combination with durable press and/or shrinkage resistance and which can be subjected to aqueous laundering.
- the water absorbency of a fabric indicates the ability of the fabric to absorb moisture, particularly surface moisture.
- good water absorbency indicates that the fabric absorbs a drop of water placed thereon, in accord with the methods described in AATCC Method 79-1995, in less than about 100 seconds.
- the fabrics employed in the present invention preferably comprise natural fibers.
- “individual fiber” refers to a short and/or thin filament, such as short filaments of cotton as obtained from the cotton boll, short filaments of wool as sheared from the sheep, filaments of cellulose or rayon, or the thin filaments of silk obtained from a silkworm cocoon.
- “fibers” is intended to include filaments in any form, including individual filaments, and the filaments present in formed yarns, fabrics and garments.
- Yarn refers to a product obtained when fibers are aligned. Yarns are products of substantial length and relatively small cross-section. Yarns may be single ply yarns, that is having one yam strand, or multiple ply yarns, such as 2-ply yarn which comprises two single yarns twisted together or 3-ply yarn which comprises three yarn strands twisted together.
- fabrics generally refer to knitted fabrics, woven fabrics, or non-woven fabrics prepared from yarns or individual fibers, while “garments” generally refer to wearable articles comprising fabrics, including, but not limited to, shirts, blouses, dresses, pants, sweaters and coats.
- Non-woven fabrics include fabrics such as felt and are composed of a web or batt of fibers bonded by the application of heat and/or pressure and/or entanglement.
- “Textiles” includes fabrics, yams, and articles comprising fabrics and/or yarns, such as garments, home goods, including, but not limited to, bed and table linens, draperies and curtains, and upholsteries, and the like.
- natural fibers refer to fibers which are obtained from natural sources, such as cellulosic fibers and protein fibers, or which are formed by the regeneration of or processing of natural occurring fibers and/or products. Natural fibers are not intended to include fibers formed from petroleum products. Natural fibers include fibers formed from cellulose, such as cotton fiber and regenerated cellulose fiber, commonly referred to as rayon, or acetate fiber derived by reacting cellulose with acetic acid and acetic anhydride in the presence of sulfuric acid. As used herein, “natural fibers” are intended to include natural fibers in any form, including individual filaments, and fibers present in yarns, fabrics and other textiles, while “individual natural fibers” is intended to refer to individual natural filaments.
- cellulosic fibers are intended to refer to fibers comprising cellulose, and include, but are not limited to, cotton, linen, flax, rayon, cellulose acetate, cellulose triacetate, hemp and ramie fibers.
- rayon fibers is intended to include, but is not limited to, fibers comprising viscose rayon, high wet modulus rayon, cuprammonium rayon, saponified rayon, modal rayon and lyocell rayon.
- Protein fibers are intended to refer to fibers comprising proteins, and include, but are not limited to, wools, such as sheep wool, alpaca, vicuna, mohair, cashmere, guanaco, camel and llama, as well as furs, suedes, and silks.
- synthetic fibers refer to those fibers which are not prepared from naturally occurring filaments and include, but are not limited to, fibers formed of synthetic materials such as polyesters, polyamides such as nylons, polyacrylics, and polyurethanes such as spandex. Synthetic fibers include fibers formed from petroleum products.
- Fabrics for use in the present invention preferably comprise natural fibers, which natural fibers may be included in any form, including, but not limited to, in the form of individual fibers (for example in nonwoven fabrics), or in the form of yarns comprising natural fibers, woven or knitted to provide the fabrics. Additionally, the fabrics may be in the form of garments or other textiles comprising natural fibers. The fabrics may further comprise synthetic fibers. Preferably, the fabrics comprise at least about 20% natural fibers. In one embodiment, the fabrics comprise at least about 50% natural fibers such as cotton fibers, rayon fibers or the like. In another embodiment, the fabrics comprise at least about 80% natural fibers such as cotton fibers, rayon fibers or the like, and in a further embodiment, the fibers comprise 100% natural fibers. Fabrics comprising cellulose fibers such as cotton and/or rayon are preferred for use in the present invention.
- the fabric is typically treated with a treatment composition comprising formaldehyde, a catalyst and a silicone elastomer or precursor thereof, followed by drying and/or curing of the treated fabric.
- a treatment composition comprising formaldehyde, a catalyst and a silicone elastomer or precursor thereof, followed by drying and/or curing of the treated fabric.
- Formaldehyde is generally available in an aqueous solution, referred to as formalin, comprising water, about 37% by weight formaldehyde, and generally about 10% to 15% by weight methanol.
- the amount of formaldehyde in the treatment composition is preferably sufficient to impart a durable press property and/or shrinkage resistance to the fabric.
- the fabric is treated with at least about 3% by weight formalin, and preferably with from about 3% to about 35% by weight formalin, based on the weight of the fabric.
- the fabric comprises cotton fibers
- the fabric is treated with about 3% to about 8% formalin, based on the weight of the fabric.
- the fabric comprises rayon fibers
- the fabric is treated with from about 10% to about 20% by weight formalin, based on the weight of the fabric.
- the fabric is treated with from about 5% to about 10%, more specifically about 8%, by weight formalin, based on the weight of the fabric.
- formalin refers to an aqueous solution comprising 37%, by weight, formaldehyde.
- formaldehyde solutions comprising levels of formaldehyde other than 37%, by weight, may also be used.
- the fabric is treated with actual formaldehyde, as opposed to formalin, at a level of from about 1% to about 13%, preferably from about 1% to about 12%, based on the weight of the fabric.
- the fabric is treated with about 1% to about 3% formaldehyde, as opposed to formalin, based on the weight of the fabric.
- the fabric comprises rayon fibers
- the fabric is treated with from about 4% to about 8% by weight formaldehyde, as opposed to formalin, based on the weight of the fabric.
- the fabric comprises a 50/50 rayon/polyester blend
- the fabric is treated with about 2% to about 4% by weight formaldehyde, as opposed to formalin, based on the weight of the fabric.
- Suitable catalysts are those capable of catalyzing a cross-linking reaction between formaldehyde and a natural fiber, and preferably are catalysts capable of catalyzing the cross-linking of formaldehyde with a natural fiber comprising hydroxy groups, such as cellulosic fibers.
- Catalysts which may be used include mineral acids, organic acids, salts of strong acids, ammonium salts, alkylamine salts, metallic salts and combinations thereof.
- the catalyst is other than a mineral acid.
- Suitable mineral acid catalysts include hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid and boric acid.
- Suitable organic acids include oxalic acid, tartaric acid, citric acid, malic acid, glycolic acid, methoxyacetic acid, chloroacetic acid, lactic acid, 3-hydroxybutyric acid, methane sulfonic acid, ethane sulfonic acid, hydroxymethane sulfonic acid, benzene sulfonic acid, p-toluene sulfonic acid, cyclopentane tetracarboxylic acid, butane tetracarboxylic acid, tetrahydrofuran-tetracarboxylic acid, nitrilotriacetic acid, and ethylenediaminetetraacetic acid.
- Suitable salts of strong acids include sodium bisulfate, sodium dihydrogen phosphate and disodium hydrogen phosphate.
- Suitable ammonium salts include ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium bisulfate, ammonium dihydrogen phosphate and diammonium hydrogen phosphate.
- Suitable alkanolamine salts include the hydrochloride, nitrate, sulfate, phosphate and sulfamate salts of 2-amino-2-methyl- 1-propanol, tris (hydroxymethyl) aminomethane and 2-amino-2-ethyl-1-3-propanediol.
- Suitable metal salts include aluminum chlorohydroxide, aluminum chloride, aluminum nitrate, aluminum sulfate, magnesium chloride, magnesium nitrate, magnesium sulfate, zinc chloride, zinc nitrate and zinc sulfate, and mixtures thereof.
- the catalyst is a halide or nitrate salt of zinc or magnesium, and preferably the catalyst is magnesium chloride.
- An organic acid such as citric acid, may be used in combination with the halide or nitrate salt of zinc or magnesium.
- the molar ratio of metal salt to organic acid is from about 5:1 to about 20:1.
- the catalyst comprises magnesium chloride and citric acid, while in another embodiment the catalyst comprises magnesium chloride and aluminum chloride.
- the fabric is typically treated with an amount of catalyst sufficient to catalyze cross-linking of the natural fibers by the formaldehyde to provide good water absorbency, and at least one of good durable press properties and/or reduced shrinkage, for example reduced shrinkage upon aqueous laundering.
- the catalyst may be employed in an amount sufficient to provide a formaldehyde:catalyst weight ratio of from about 10:1 to about 1:10, and preferably from about 5:1 to about 1:5.
- the formaldehyde treatment composition may comprise, by weight, up to about 12% of a catalyst solution, and preferably from about 1% to about 9% of a catalyst solution.
- the catalyst solution comprises from about 20% to about 50%, by weight catalyst.
- the treatment solution comprises from about 2 to about 4% by weight of a catalyst solution comprising about 30% by weight catalyst
- the treatment solution comprises from about 6% to about 8% by weight of a catalyst solution comprising about 30% by weight catalyst.
- the catalyst solution comprises about 40%, by weight, magnesium chloride, for a final magnesium chloride level of up to about 5%, by weight of the treatment solution.
- Suitable catalyst solutions include FREECAT® LF (magnesium chloride and citric acid) and FREECAT® No. 9 (aluminum chloride and magnesium chloride), commercially available from B. F. Goodrich.
- the formaldehyde treatment composition typically comprises a liquid carrier, preferably water, although, as noted above, the formalin used to prepare the treatment composition may comprise small amounts of organic solvents such as methanol or the like. In one embodiment, the treatment composition is free of any organic solvents other than that present in the formalin or the catalyst solution. In another embodiment, the carrier may comprise pentamethylcyclosiloxane.
- a silicone elastomer or precursor thereof is included in the formaldehyde-containing treatment composition with which the fabric is treated.
- the formaldehyde treatment composition comprises formaldehyde, catalyst and silicone elastomer or a precursor thereof. It has been discovered that the combination of a silicone elastomer or precursor thereof and the formaldehyde-containing treatment composition provides the fabric with good water absorbency, while also providing good durable press and/or shrinkage resistance properties. This is remarkable in that many conventional durable press and/or shrinkage resistance treatments render the treated fabrics hydrophobic.
- the silicone elastomer may also be effective to reduce the loss in tear and tensile strength that typically occurs during formaldehyde cross-linking of fibers.
- the silicone elastomer is a polysiloxane.
- the silicone elastomer precursor which forms an elastomer upon curing, typically by self curing may be a polysiloxane.
- Elastomers are polymers which are capable of being stretched with relatively little applied force, and which return to the unstretched length when the force is released. Silicone elastomers have a backbone made of silicon and oxygen with organic substituents attached to silicon atoms, with a number n of repeating units of the general formula:
- the groups R and R ⁇ are each independently selected from lower alkyls, preferably C 1 -C 3 alkyls, phenyl, or lower alkyls or phenyls comprising a group reactive to cellulose, such as hydroxy groups, halogen atoms, for example, fluoride, or amino groups.
- Suitable elastomers include those disclosed in U.S. Pat. No. 5,885,303, incorporated herein by reference.
- a preferred silicone elastomer or precursor composition comprises up to about 60%, by weight, silicone solids.
- the silicone elastomer or precursor composition comprises from about 20% to about 60%, preferably from about 30% to about 60%, by weight of silicone solids, while in another embodiment the silicone elastomer or precursor composition comprises from about 20% to about 30% by weight of silicone solids.
- Suitable silicone elastomer precursors include a dimethyl silicone emulsion containing from about 30% to about 60%, by weight, silicone solids, commercially available as SM2112 from General Electric.
- Another suitable commercially available elastomer precursor is Sedgesoft ELS from Sedgefield Specialties, containing from about 24% to about 26%, by weight, silicone solids.
- the liquid treatment composition may comprise up to about 10%, preferably from about 1% to about 5%, more preferably from about 1% to about 3%, by weight of the elastomer or precursor solids.
- the treatment composition comprises from about 1% to about 3%, preferably from about 1.5% to 3%, by weight silicone solids, while in another embodiment, the composition comprises from about 1% to about 1.5% by weight silicone solids.
- the formaldehyde treatment composition may be applied to the fabric in accordance with any of the conventional techniques known in the art.
- the treatment composition may be applied to the fabric by saturating the fabric in a trough and squeezing the saturated fabric through pressure rollers to achieve a uniform application (padding process).
- wet pick-up refers to the amount of treatment composition applied to and/or absorbed into the fabric based on the original weight of the fabric.
- “Original weight of the fabric” or simply “weight of the fabric” refers to the weight of the fabric prior to its contact with the treatment composition.
- 50% pick-up means that the fabric picks up an amount of treatment solution equal to 50% of the fabric's original weight.
- the wet pick-up is at least 20%, preferably from about 50% to 100%, more preferably from about 65% to about 80%, by weight of the fabric.
- the formaldehyde treatment composition is applied in an amount to insure a moisture content of more than 20% by weight, preferably more than 30% by weight, on the fabric before curing.
- a wetting agent may be included in the treatment composition to facilitate obtaining the desired moisture content. Nonionic wetting agents are preferred.
- the fabric is typically heated for a time and at a temperature sufficient for the cross-linking of the natural fibers with the formaldehyde.
- the fabric may be heated at a temperature greater than about 250 ⁇ F, preferably from about 250 ⁇ F to about 350 ⁇ F, in an oven for a period of from about 15 seconds to about 15 minutes, preferably from about 45 seconds to about 3 minutes, to react the formaldehyde with the natural fibers in the fabric and affect crosslinking of the formaldehyde and natural fibers to provide durable press and/or shrinkage resistance effects.
- curing temperature and curing time that is, the higher the temperature of curing, the shorter the dwell time in the oven; conversely, the lower the curing temperature, the longer the dwell time in the oven.
- the present invention comprises methods for improving the water absorbency of fabric, wherein the silicone elastomer may be included in the treated fabric by means of a separate treatment step before or after the formaldehyde crosslinking treatment. Additionally, if the silicone elastomer or precursor thereof is applied to the fabric subsequent to treatment with the formaldehyde crosslinking composition, the silicone elastomer precursor thereof may be applied prior to or subsequent to the heating step which is employed to affect curing of the formaldehyde with the natural fibers of the fabric, although application prior to heating is preferred. The applied silicone elastomer or precursor thereof may be dried, with self curing of the precursor being affected thereby.
- the fabrics according to the present invention exhibit good water absorbency. As noted above this indicates that the fabrics exhibit a water absorbency time, in accord with the methods described in AATCC Method 79-1995, of less than about 100 seconds. In a more specific embodiment, the fabrics according to the present invention exhibit a water absorbency time, in accord with the methods described in AATCC Method 79-1995, of less than about 80 seconds, even after the fabric has been aqueous laundered at least once. In yet a further embodiment, the fabrics according to the present invention exhibit a water absorbency time, in accord with the methods described in AATCC Method 79-1995, of less than about 60 seconds, even after the fabric has been aqueous laundered at least once.
- wetting agents may be employed to improve wet pick-up of chemistry during fabric finishing.
- the water absorbency properties as disclosed herein are exhibited by the fabric after any such wetting agent has been removed, for example by laundering or the like. Thus, the good water absorbency properties are maintained after one or more washings or launderings of the fabrics.
- the good water absorbency properties are particularly advantageous when the fabric is used in garment manufacture, as garments which absorb moisture are generally more comfortable for wear and therefore are preferred by consumers over garments which are formed of hydrophobic, non-moisture absorbing fabrics.
- the fabrics according to the invention also exhibit good durable press properties and/or good shrink resistance.
- the fabric exhibit good durable press, for example a DP (durable press) rating of at least about 3.0, preferably at least about 3.25, and more preferably at least about 3.5, as measured according to AATCC Test Method 124-1996, after one aqueous washing, more preferably after five aqueous washings, and/or good shrinkage resistance, for example a length shrinkage and a width shrinkage of less than about 10% each, preferably less than about 5% each, more preferably less than about 4% each, and even more preferably less than about 2% each, and in certain embodiments, less than about 1% each, as measured according to AATCC Test Method 135-1995, after one machine washing, more preferably after five aqueous washings.
- DP durable press
- Shrinkage resistance may also be measured according to AATCC Test Method 150-1995.
- the fabrics exhibit good filling tensile and tear strengths, for example of at least about 25 pounds and at least about 24 ounces, respectively, as measured according to ASTM D- 5035-95 for tensile strength, and ASTM D-2261-96 for tear strength.
- cellulose fabrics having a crosslinked formaldehyde treatment and exhibiting good water absorbency, even after laundering, are obtained, provided that the fabric does not comprise 100% cotton.
- These fabrics may comprise greater than about 20% cotton fibers, greater than about 50% cotton fibers, greater than about 80% cotton fibers, greater than about 20% rayon fibers, greater than about 50% rayon fibers, greater than about 80% rayon fibers, or about 100% rayon fibers.
- the fabrics according to the invention exhibit good hand or softness, in the absence of conventional softeners such as silicone or polyethylene softeners. Typically, the fabrics will exhibit a low coefficient of friction and/or a high flexibility/Instron softness.
- unreacted formaldehyde remaining on the fabric is removed during subsequent processing of the fabric.
- the final substrate will comprise less than about 300 ppm formaldehyde, preferably less than about 200 ppm formaldehyde, more preferably less than about 100 ppm formaldehyde, and even more preferably less than about 50 ppm formaldehyde, as measured according to AATCC Test Method 112-1993.
- silicone oils include, for example, non-reactive linear polydimethyl siloxanes, that is, siloxanes which are not capable of further reaction with other silicones and are not capable of a self curing reaction. Silicone oils have a tendency to produce non-removable spots on fabrics. In contrast, the silicone elastomers used in the present invention generally do not produce such spots.
- the fabrics or treatment compositions may comprise silicone oil, in one embodiment, the fabrics and treatment compositions are substantially free of, and preferably are free of, silicone oil. As used herein, substantially free of silicone oils means the treatment compositions and fabrics comprise less than 1%, by weight, silicone oil.
- Thermosetting resins used to impart durable press properties to fabrics are generally aminoplast resins which are the products of the reaction of formaldehyde with compounds such as urea, thiourea, ethylene urea, dihydroxyethylene urea and melamines.
- aminoplast resins is intended to include N-methylolamide cross-linking agents such as dimethylol dihydroxyethylene urea, dimethylol urea, dimethylolethylene urea, dimethylol propylene urea, dimethylol methyl carbamate, dimethylol n-propylcarbamate, dimethylol isopropylcarbamate trimethylolated melamine, and tris(methoxymethol) melamine.
- the fabrics, methods and formaldehyde treatment compositions of the invention are substantially free of, and more preferably are free of, aminoplast resins and N-methylol cross-linking agents.
- substantially free of aminoplast resins and N-methylol cross-linking agents is intended to mean the fabrics and treatment solutions comprise less than about 0.5%, by weight, aminoplast resin or methylol cross-linking agent.
- the fabric Prior to treatment with the formaldehyde composition and silicone elastomer or precursor thereof, the fabric may optionally be prepared using any fiber, yarn, or textile pre-treatment preparation techniques known in the art. Suitable preparation techniques include brushing, singeing, desizing, scouring, mercerizing, and bleaching.
- fabric may be treated by brushing which refers to the use of mechanical means for raising surface fibers which will be removed during singeing. The fabric may be then be singed using a flame to burn away fibers and fuzz protruding from the fabric surface.
- Textiles may be desized, which refers to the removal of sizing chemicals such as starch and/or polyvinyl alcohol, that are put on yarns prior to weaving to protect individual yarns.
- the fabrics may be scoured, which refers to the process of removing natural impurities such as oils, fats and waxes and synthetic impurities such as mill grease from fabrics.
- Mercerization refers to the application of high concentrations of sodium hydroxide to a fabric to alter the morphology of fibers, particularly cotton fibers. Fabrics may be mercerized to improve fabric stability and luster.
- bleaching refers to the process of destroying any natural color bodies within the natural fiber.
- a typical bleaching agent is hydrogen peroxide.
- the various preparation techniques are optional and dependent upon the desired final product. For example, when the final fabric is to be dyed a dark color, there may be no need to bleach the substrate. Similarly, there may be no need to desize a knit which was prepared without using any sizing agents, and no need to separately scour knits and woven textiles as the scouring may be done during bleaching.
- rayon fabric samples are provided with a formaldehyde crosslinking treatment in accordance with the invention.
- each fabric is contacted with an aqueous solution comprising about 10% to 20% formalin, a weight ratio of formalin to catalyst solution of about 18:5, and about 3% (solids) of a silicone elastomer commercially available from General Electric under the designation GE SM2112.
- the aqueous solution is padded on the fabric to provide a moisture content of greater than about 30% and the treated fabric is heated at a temperature greater than about 300° F. for a period of time sufficient to effect crosslinking of the formaldehyde with the cellulose in the rayon fabrics.
- the water absorbency properties of various fabrics are measured according to AATCC Method 79-1995.
- a drop of water is placed on the fabric surface and the time taken for the specular reflection of the drop to disappear is measured as an indication of the water absorbency of the fabric. The shorter the time, the better the water absorbency of the fabric.
- the first fabric comprises a Tencel® lyocell fabric
- the second fabric comprises an 85/15 rayon/flax blend
- the third fabric comprises 100% viscose rayon fabric, all of which are treated generally in accord with the method described in Example 1.
- An aqueous bath solution comprising about 35% formalin, 10% of a 30% catalyst solution and 5% of a silicone elastomer, Glosil ECR from Glotex Chemical, is employed.
- the solution further comprises about 1% of a wetting agent.
- the treated fabrics are cured at about 350 ⁇ F.
- untreated samples of each fabric and samples of each fabric provided with a conventional aminoplast resin and silicone softener combination treatment are also subjected to measurement of their water absorbency properties.
- the aminoplast treated fabric samples are prepared using a bath solution comprising a conventional aminoplast resin, BF Goodrich Free Res 845 (6%), a conventional cationic fatty amide softener, Fabritone HC (8%), and silicone elastomer/softener, Glosil ECR (2%) from Glotex Chemical.
- the bath solution further comprises about 1% of a wetting agent.
- the water absorbency of each fabric type is measured initially, before any laundering of the treated or untreated fabric, after one wash cycle at 60° F., after five wash cycles at 60° F., after one wash cycle at 95° F., and after five wash cycles at 95° F.
- the water absorbency of five samples of each fabric type are measured at the specified conditions and the average of the measured values in seconds is set forth in Table 1, with the standard deviation of the measured values being set forth in parentheses. TABLE 1 Water Absorbency, Seconds No wash One Wash, Five Washes, One Wash, Five Washes, Fabric Sample cycle 60° F. 60° F. 95° F. 95° F.
- the untreated fabrics all absorb water very rapidly, regardless of the number of washings to which they were subjected.
- these untreated materials are disadvantageous as they do not exhibit good durable press properties and/or good shrinkage resistance and/or, as often in the case of Tencel®, do not exhibit good appearance after laundering.
- the fabrics treated according to the present methods (formaldehyde treated) all exhibit good water absorbency, both before and after one or more washings. These fabrics are also advantageous in that they exhibit good durable press properties and good shrinkage resistance.
- the aminoplast resin treated fabrics exhibit good water absorbency properties prior to washing, it is believed that this good water absorbency is due to the presence of residual wetting agent from the aqueous resin treatment on the fabric surface. Once the aminoplast resin-treated fabrics are subjected to washing, wherein residual wetting agent is removed, the fabrics exhibit extremely poor water absorbency.
- the times of greater than 360 seconds indicate that the fabrics exhibit poor water absorbency.
- Viscose Aminoplast resin (15%) 1 ⁇ 1 ⁇ 1 2.0 3.8 ⁇ 1.5 2 Viscose Aminoplast resin (7.5%) ⁇ 1 ⁇ 1 1.1 9.4 ⁇ 6.0 3 Viscose Aminoplast resin (22%) ⁇ 1 ⁇ 1 1.5 2.8 ⁇ 1.4 4 Viscose Untreated ⁇ 1 ⁇ 1 1.0 10.8 ⁇ 7.5 5 Viscose Aminoplast resin (15%) + >270 >300 2.1 3.8 ⁇ 3.7 Si softener (3%) 2 6 Viscose Aminoplast resin (15%) + ⁇ 1 ⁇ 1 2.4 4.1 ⁇ 1.6 PE softener (3%) 3 7 Viscose Aminoplast resin (15%) + 100 >300 1.9 3.9 ⁇ 3.4 Si softener (3%) + PE softener (3%) 8 Viscose Aminoplast resin (15%) + 93 >300 2.5 3.4 ⁇ 1.8 Si softener (4.5%) + PE softener (4.5%) 9 Viscose Aminoplast resin (15%) (15%)
- samples 11, 15 and 17 are according to the present invention and are treated with both formaldehyde (formalin) and silicone elastomer.
- a catalyst is employed in an approximately 3:1 ratio with the formaldehyde. Water absorbency is tested prior to any washing of the fabric and after one wash cycle conducted at about 95 ⁇ F.
- the rayon fabric samples of samples 11, 15 and 17 according to the invention exhibit excellent water absorbency, particularly after washing, good durable press and good shrinkage resistance.
- comparative fabric samples 5, 7-10, 14 and 16 are further unacceptable for consumer use in view of their very poor water absorbency.
- water absorbency times of greater than about 300 seconds indicate that the fabrics exhibit poor water absorbency.
- silicone softeners which are conventionally used to improve the feel of aminoplast resin-treated fabrics, contribute to the poor water absorbency of the fabrics.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Methods for providing fabric with good water absorbency and durable press properties comprise treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde. Methods for providing fabric with good water absorbency and shrinkage resistance properties comprise treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde. Fabrics having good water absorbency in combination with additional advantageous properties are produced.
Description
- This application claims priority under 37 U.S.C. § 119(e) to U.S. Provisional Application Ser. No. 60/192,903, filed Mar. 29, 2000 (Attorney Docket No.8008P).
- This invention relates to methods for providing fabrics, particularly fabrics containing natural fibers such as cotton, rayon and the like, with good water absorbency in combination with durable press and/or shrinkage resistance. This invention also relates to cellulose fabrics which have improved water absorbency, particularly in combination with good durable press properties and/or shrinkage resistance.
- Many fabrics, particularly fabrics comprising natural fibers, do not possess durable press (or “wash and wear” or “smooth-dry”) performance or dimensional stability, i.e., shrinkage resistance. Cellulosic fabrics such as cotton have been treated with aminoplast resins, including N-methylol cross-linking resins such as dimethylol dihydroxyethyleneurea (DMDHEU) or dimethylol propylcarbamate (DMPC), to impart durable press properties, as disclosed, for example, in the Martin et al U.S. Pat. No. 4,521,176. Unfortunately, many reacted aminoplast resins break down during storage, thus releasing formaldehyde. The formaldehyde release may occur not only throughout the preparation of the fabric but also during garment-making. Further, garments or fabrics treated with aminoplast resins may release additional formaldehyde when stored under humid conditions. Aminoplast resins may also hydrolyze during washing procedures, resulting in a loss of the durable press performance. Additionally, aminoplast resins tend to give fabric a harsher handle, that is, make the fabric feel less soft. As the resins make the fabric feel less soft, the fabric must be treated with additional softeners, for example silicone softeners. Unfortunately, the silicone softeners tend to make the fabric hydrophobic although it is often preferred that the fabric have hydrophilic properties.
- Cellulosic fibers have also been cross-linked with formaldehyde to impart durable press properties. For example, the Payet U.S. Pat. Nos. 3,960,482, 3,960,483, 4,067,688 and 4,104,022 disclose durable press processes which comprise impregnating a cellulosic fiber-containing fabric with an aqueous solution comprising a catalyst, and, while the fabric has a moisture content of above 20% by weight, exposing the fabric to formaldehyde vapors and curing under conditions at which formaldehyde reacts with the cellulose. The Payet U.S. Pat. No. 4,108,598 discloses a process which comprises treating cellulosic fiber-containing fabrics with an aqueous solution of formaldehyde and a catalyst, heat curing the treated fabric by introducing the fabric into a heating zone, and gradually increasing the temperature of the heating zone, thereby increasing the temperature of the heated fabric to prevent the loss of an amount of formaldehyde which will reduce the overall extent of curing. The Payet U.S. Pat. No. 5,885,303 also discloses a durable press process for cellulosic fiber-containing fabrics. The process comprises treating the fabric with an aqueous solution of formaldehyde, a catalyst capable of catalyzing the cross-linking reaction between formaldehyde and cellulose, and an effective amount of a silicone elastomer to reduce loss in tear strength in the treated fabric. Formaldehyde is generally less expensive than aminoplast resins, and formaldehyde treatment of cellulosic fabrics typically results in durable press properties which are more durable than those obtained by aminoplast resins.
- Rayon garments are desirable by consumers for a variety of reasons. However, many durable press treatment processes that have been provided for cotton cellulosic fabrics have not been suitable for rayon fabrics. Although rayon and cotton are both cellulosic fibers, they react very differently from one another. Particularly, rayon-containing fabrics exhibit significant shrinkage when subjected to aqueous washing or laundering and therefore generally require dry cleaning as opposed to washing in an aqueous environment.
- The copending Payet application Ser. No. 09/163,319 discloses processes for providing rayon fabrics with durable press properties wherein a rayon fiber-containing fabric is treated with an aqueous mixture containing a high concentration of formaldehyde and a catalyst capable of catalyzing the cross-linking reaction between formaldehyde and the rayon, and the treated fabric is heat cured. Payet discloses that the fabric may be washed or laundered in an aqueous system and does not shrink substantially on aqueous washing. Additionally, a silicone elastomer may be employed to reduce loss in tear and tensile strength in the treated fabric.
- An important feature of cellulose fabrics, both cotton and rayon particularly, is that they are naturally hydrophilic, and therefore absorb moisture. Typically, garments made of fabrics which are hydrophilic are more comfortable for wear and therefore are preferred by consumers over garments which are formed of hydrophobic, non-moisture absorbing fabrics. However, many conventional fabric treatments for improving durable press and/or for reducing shrinkage of cellulose fabrics, and particularly for cotton and rayon fabrics, inhibit the natural water absorbency of the cellulose fibers and render the fabrics hydrophobic. Such fabrics are therefore not preferred for garment use owing to their reduced ability or substantial inability to absorb moisture.
- Accordingly, there is a continuing need to further improve individual characteristics of fabrics containing natural fibers, for example cotton and rayon, and to improve the overall combinations of properties exhibited by such fabrics.
- Accordingly, it is an object of the present invention to obviate problems of the prior art. It is a further object of the present invention to provide methods for improving the water absorbency of fabrics and particularly to improve the water absorbency of treated fabrics containing natural fibers, i.e., fabrics which are treated to provide additional advantageous properties, for example durable press properties and/or shrinkage resistance. It is a related object to provide methods for preparing fabrics which exhibit advantageous combinations of properties and which are suitable for aqueous washing or laundering, and to provide cellulose fabrics which exhibit advantageous combinations of properties and which are suitable for aqueous washing or laundering.
- These and additional objects are provided by the methods and fabrics of the invention. In one embodiment, the invention is directed to methods for providing fabric with good water absorbency and durable press properties, which methods comprise treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde. In another embodiment, the invention is directed to methods for providing fabric with good water absorbency and shrinkage resistance properties, which methods comprising treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde. In a further embodiment, the invention is directed to methods for providing rayon fabric with reduced shrinkage and good water absorbency, which methods comprise crosslinking cellulose in the fabric with formaldehyde and providing the fabric with a silicone elastomer. In yet additional embodiments, the invention is directed to fabric comprising rayon fibers and exhibiting a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time, and to fabric comprising cotton fibers and having a crosslinked formaldehyde durable press treatment and exhibiting a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time, wherein the fabric does not comprise 100% cotton.
- The methods of the invention are advantageous in providing fabrics which exhibit good water absorbency, particularly in combination with other desirable properties, for example durable press properties and/or shrinkage reduction.
- These and additional aspects, objects and advantages of the invention are more fully described in the detailed description.
- The present invention is directed to methods for providing fabrics, particularly fabrics comprising natural fibers, with good water absorbency in combination with good durable press properties and/or shrinkage resistance. This invention also relates to fabrics which have good water absorbency, particularly in combination with durable press and/or shrinkage resistance and which can be subjected to aqueous laundering.
- As is known in the art, the water absorbency of a fabric indicates the ability of the fabric to absorb moisture, particularly surface moisture. As employed in the present invention, good water absorbency indicates that the fabric absorbs a drop of water placed thereon, in accord with the methods described in AATCC Method 79-1995, in less than about 100 seconds.
- The fabrics employed in the present invention preferably comprise natural fibers. As used herein, “individual fiber” refers to a short and/or thin filament, such as short filaments of cotton as obtained from the cotton boll, short filaments of wool as sheared from the sheep, filaments of cellulose or rayon, or the thin filaments of silk obtained from a silkworm cocoon. As used herein, “fibers” is intended to include filaments in any form, including individual filaments, and the filaments present in formed yarns, fabrics and garments.
- As used herein, “yarn” refers to a product obtained when fibers are aligned. Yarns are products of substantial length and relatively small cross-section. Yarns may be single ply yarns, that is having one yam strand, or multiple ply yarns, such as 2-ply yarn which comprises two single yarns twisted together or 3-ply yarn which comprises three yarn strands twisted together. As used herein, “fabrics” generally refer to knitted fabrics, woven fabrics, or non-woven fabrics prepared from yarns or individual fibers, while “garments” generally refer to wearable articles comprising fabrics, including, but not limited to, shirts, blouses, dresses, pants, sweaters and coats. Non-woven fabrics include fabrics such as felt and are composed of a web or batt of fibers bonded by the application of heat and/or pressure and/or entanglement. “Textiles” includes fabrics, yams, and articles comprising fabrics and/or yarns, such as garments, home goods, including, but not limited to, bed and table linens, draperies and curtains, and upholsteries, and the like.
- As used herein, “natural fibers” refer to fibers which are obtained from natural sources, such as cellulosic fibers and protein fibers, or which are formed by the regeneration of or processing of natural occurring fibers and/or products. Natural fibers are not intended to include fibers formed from petroleum products. Natural fibers include fibers formed from cellulose, such as cotton fiber and regenerated cellulose fiber, commonly referred to as rayon, or acetate fiber derived by reacting cellulose with acetic acid and acetic anhydride in the presence of sulfuric acid. As used herein, “natural fibers” are intended to include natural fibers in any form, including individual filaments, and fibers present in yarns, fabrics and other textiles, while “individual natural fibers” is intended to refer to individual natural filaments.
- As used herein, “cellulosic fibers” are intended to refer to fibers comprising cellulose, and include, but are not limited to, cotton, linen, flax, rayon, cellulose acetate, cellulose triacetate, hemp and ramie fibers. As used herein, “rayon fibers” is intended to include, but is not limited to, fibers comprising viscose rayon, high wet modulus rayon, cuprammonium rayon, saponified rayon, modal rayon and lyocell rayon. “Protein fibers” are intended to refer to fibers comprising proteins, and include, but are not limited to, wools, such as sheep wool, alpaca, vicuna, mohair, cashmere, guanaco, camel and llama, as well as furs, suedes, and silks.
- As used herein, “synthetic fibers” refer to those fibers which are not prepared from naturally occurring filaments and include, but are not limited to, fibers formed of synthetic materials such as polyesters, polyamides such as nylons, polyacrylics, and polyurethanes such as spandex. Synthetic fibers include fibers formed from petroleum products.
- Fabrics for use in the present invention preferably comprise natural fibers, which natural fibers may be included in any form, including, but not limited to, in the form of individual fibers (for example in nonwoven fabrics), or in the form of yarns comprising natural fibers, woven or knitted to provide the fabrics. Additionally, the fabrics may be in the form of garments or other textiles comprising natural fibers. The fabrics may further comprise synthetic fibers. Preferably, the fabrics comprise at least about 20% natural fibers. In one embodiment, the fabrics comprise at least about 50% natural fibers such as cotton fibers, rayon fibers or the like. In another embodiment, the fabrics comprise at least about 80% natural fibers such as cotton fibers, rayon fibers or the like, and in a further embodiment, the fibers comprise 100% natural fibers. Fabrics comprising cellulose fibers such as cotton and/or rayon are preferred for use in the present invention.
- While not being bound by theory, it is believed that when natural fibers are treated with a composition comprising formaldehyde and a catalyst capable of cross-linking formaldehyde with a natural fiber, a chemical modification of the natural fibers occurs. It is believed that the formaldehyde reacts chemically with the natural fibers to cross-link the individual polymer chains of the natural fibers, and establish the durable press properties and/or dimensional stability, i.e., reduced shrinkage. In accordance with the present methods, a silicone elastomer or precursor thereof is included in the formaldehyde treatment and the fabrics exhibit good water absorbency. The fabrics preferably also exhibit good strength, for example good tear strength.
- To provide the crosslinked formaldehyde treatment, the fabric is typically treated with a treatment composition comprising formaldehyde, a catalyst and a silicone elastomer or precursor thereof, followed by drying and/or curing of the treated fabric. Formaldehyde is generally available in an aqueous solution, referred to as formalin, comprising water, about 37% by weight formaldehyde, and generally about 10% to 15% by weight methanol.
- The amount of formaldehyde in the treatment composition is preferably sufficient to impart a durable press property and/or shrinkage resistance to the fabric. Generally the fabric is treated with at least about 3% by weight formalin, and preferably with from about 3% to about 35% by weight formalin, based on the weight of the fabric. In one embodiment, for example wherein the fabric comprises cotton fibers, the fabric is treated with about 3% to about 8% formalin, based on the weight of the fabric. In another embodiment, for example wherein the fabric comprises rayon fibers, the fabric is treated with from about 10% to about 20% by weight formalin, based on the weight of the fabric. In yet another embodiment, for example wherein the fabric comprises a 50/50 rayon/polyester blend, the fabric is treated with from about 5% to about 10%, more specifically about 8%, by weight formalin, based on the weight of the fabric. As used herein, “formalin” refers to an aqueous solution comprising 37%, by weight, formaldehyde. As will be apparent to one of skill in the art, formaldehyde solutions comprising levels of formaldehyde other than 37%, by weight, may also be used. Using the above ranges of formalin, the fabric is treated with actual formaldehyde, as opposed to formalin, at a level of from about 1% to about 13%, preferably from about 1% to about 12%, based on the weight of the fabric. Thus, in one embodiment, for example wherein the fabric comprises cotton fibers, the fabric is treated with about 1% to about 3% formaldehyde, as opposed to formalin, based on the weight of the fabric. In another embodiment, for example wherein the fabric comprises rayon fibers, the fabric is treated with from about 4% to about 8% by weight formaldehyde, as opposed to formalin, based on the weight of the fabric. In yet another embodiment, wherein the fabric comprises a 50/50 rayon/polyester blend, the fabric is treated with about 2% to about 4% by weight formaldehyde, as opposed to formalin, based on the weight of the fabric.
- Suitable catalysts are those capable of catalyzing a cross-linking reaction between formaldehyde and a natural fiber, and preferably are catalysts capable of catalyzing the cross-linking of formaldehyde with a natural fiber comprising hydroxy groups, such as cellulosic fibers. Catalysts which may be used include mineral acids, organic acids, salts of strong acids, ammonium salts, alkylamine salts, metallic salts and combinations thereof. In one embodiment the catalyst is other than a mineral acid.
- Suitable mineral acid catalysts include hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid and boric acid. Suitable organic acids include oxalic acid, tartaric acid, citric acid, malic acid, glycolic acid, methoxyacetic acid, chloroacetic acid, lactic acid, 3-hydroxybutyric acid, methane sulfonic acid, ethane sulfonic acid, hydroxymethane sulfonic acid, benzene sulfonic acid, p-toluene sulfonic acid, cyclopentane tetracarboxylic acid, butane tetracarboxylic acid, tetrahydrofuran-tetracarboxylic acid, nitrilotriacetic acid, and ethylenediaminetetraacetic acid. Suitable salts of strong acids include sodium bisulfate, sodium dihydrogen phosphate and disodium hydrogen phosphate. Suitable ammonium salts include ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium bisulfate, ammonium dihydrogen phosphate and diammonium hydrogen phosphate. Suitable alkanolamine salts include the hydrochloride, nitrate, sulfate, phosphate and sulfamate salts of 2-amino-2-methyl- 1-propanol, tris (hydroxymethyl) aminomethane and 2-amino-2-ethyl-1-3-propanediol. Suitable metal salts include aluminum chlorohydroxide, aluminum chloride, aluminum nitrate, aluminum sulfate, magnesium chloride, magnesium nitrate, magnesium sulfate, zinc chloride, zinc nitrate and zinc sulfate, and mixtures thereof.
- In one embodiment of the invention, the catalyst is a halide or nitrate salt of zinc or magnesium, and preferably the catalyst is magnesium chloride. An organic acid, such as citric acid, may be used in combination with the halide or nitrate salt of zinc or magnesium. Generally the molar ratio of metal salt to organic acid is from about 5:1 to about 20:1. In one embodiment, the catalyst comprises magnesium chloride and citric acid, while in another embodiment the catalyst comprises magnesium chloride and aluminum chloride.
- The fabric is typically treated with an amount of catalyst sufficient to catalyze cross-linking of the natural fibers by the formaldehyde to provide good water absorbency, and at least one of good durable press properties and/or reduced shrinkage, for example reduced shrinkage upon aqueous laundering. In one embodiment, the catalyst may be employed in an amount sufficient to provide a formaldehyde:catalyst weight ratio of from about 10:1 to about 1:10, and preferably from about 5:1 to about 1:5.
- The formaldehyde treatment composition may comprise, by weight, up to about 12% of a catalyst solution, and preferably from about 1% to about 9% of a catalyst solution. Generally the catalyst solution comprises from about 20% to about 50%, by weight catalyst. In one embodiment, for example wherein the fabric comprises cotton fibers, the treatment solution comprises from about 2 to about 4% by weight of a catalyst solution comprising about 30% by weight catalyst, and in another embodiment, for example wherein the fabric comprises rayon fibers, the treatment solution comprises from about 6% to about 8% by weight of a catalyst solution comprising about 30% by weight catalyst. In yet a further embodiment, the catalyst solution comprises about 40%, by weight, magnesium chloride, for a final magnesium chloride level of up to about 5%, by weight of the treatment solution. Suitable catalyst solutions include FREECAT® LF (magnesium chloride and citric acid) and FREECAT® No. 9 (aluminum chloride and magnesium chloride), commercially available from B. F. Goodrich.
- The formaldehyde treatment composition typically comprises a liquid carrier, preferably water, although, as noted above, the formalin used to prepare the treatment composition may comprise small amounts of organic solvents such as methanol or the like. In one embodiment, the treatment composition is free of any organic solvents other than that present in the formalin or the catalyst solution. In another embodiment, the carrier may comprise pentamethylcyclosiloxane.
- According to the present methods, a silicone elastomer or precursor thereof is included in the formaldehyde-containing treatment composition with which the fabric is treated. Thus, the formaldehyde treatment composition comprises formaldehyde, catalyst and silicone elastomer or a precursor thereof. It has been discovered that the combination of a silicone elastomer or precursor thereof and the formaldehyde-containing treatment composition provides the fabric with good water absorbency, while also providing good durable press and/or shrinkage resistance properties. This is remarkable in that many conventional durable press and/or shrinkage resistance treatments render the treated fabrics hydrophobic. The silicone elastomer may also be effective to reduce the loss in tear and tensile strength that typically occurs during formaldehyde cross-linking of fibers.
- Various silicone elastomers are known in the art and are suitable for use in the methods and fabrics of the invention. In one embodiment, the silicone elastomer is a polysiloxane. Similarly, the silicone elastomer precursor which forms an elastomer upon curing, typically by self curing, may be a polysiloxane. Elastomers are polymers which are capable of being stretched with relatively little applied force, and which return to the unstretched length when the force is released. Silicone elastomers have a backbone made of silicon and oxygen with organic substituents attached to silicon atoms, with a number n of repeating units of the general formula:
- The groups R and Rÿ are each independently selected from lower alkyls, preferably C1-C3 alkyls, phenyl, or lower alkyls or phenyls comprising a group reactive to cellulose, such as hydroxy groups, halogen atoms, for example, fluoride, or amino groups. Suitable elastomers include those disclosed in U.S. Pat. No. 5,885,303, incorporated herein by reference.
- A preferred silicone elastomer or precursor composition comprises up to about 60%, by weight, silicone solids. In one embodiment, the silicone elastomer or precursor composition comprises from about 20% to about 60%, preferably from about 30% to about 60%, by weight of silicone solids, while in another embodiment the silicone elastomer or precursor composition comprises from about 20% to about 30% by weight of silicone solids. Suitable silicone elastomer precursors include a dimethyl silicone emulsion containing from about 30% to about 60%, by weight, silicone solids, commercially available as SM2112 from General Electric. Another suitable commercially available elastomer precursor is Sedgesoft ELS from Sedgefield Specialties, containing from about 24% to about 26%, by weight, silicone solids.
- When the silicone elastomer or precursor thereof is applied to the fabric with a liquid formaldehyde treatment composition, the liquid treatment composition may comprise up to about 10%, preferably from about 1% to about 5%, more preferably from about 1% to about 3%, by weight of the elastomer or precursor solids. In one embodiment, the treatment composition comprises from about 1% to about 3%, preferably from about 1.5% to 3%, by weight silicone solids, while in another embodiment, the composition comprises from about 1% to about 1.5% by weight silicone solids.
- The formaldehyde treatment composition may be applied to the fabric in accordance with any of the conventional techniques known in the art. In one embodiment, the treatment composition may be applied to the fabric by saturating the fabric in a trough and squeezing the saturated fabric through pressure rollers to achieve a uniform application (padding process). As used herein “wet pick-up” refers to the amount of treatment composition applied to and/or absorbed into the fabric based on the original weight of the fabric. “Original weight of the fabric” or simply “weight of the fabric” refers to the weight of the fabric prior to its contact with the treatment composition. For example, 50% pick-up means that the fabric picks up an amount of treatment solution equal to 50% of the fabric's original weight. Preferably the wet pick-up is at least 20%, preferably from about 50% to 100%, more preferably from about 65% to about 80%, by weight of the fabric.
- Other application techniques which may be employed include kiss roll application, engraved roll application, printing, foam finishing, vacuum extraction, spray application or any process known in the art. Generally theses techniques provide lower wet pick-up than the padding process. The concentration of the chemicals in the solution may be adjusted to provide the desired amount of chemicals on the original weight of the fabric (OWF).
- In a preferred embodiment, the formaldehyde treatment composition is applied in an amount to insure a moisture content of more than 20% by weight, preferably more than 30% by weight, on the fabric before curing. Optionally, a wetting agent may be included in the treatment composition to facilitate obtaining the desired moisture content. Nonionic wetting agents are preferred.
- Once the treatment composition has been applied to the fabric, the fabric is typically heated for a time and at a temperature sufficient for the cross-linking of the natural fibers with the formaldehyde. For example, the fabric may be heated at a temperature greater than about 250ÿF, preferably from about 250ÿF to about 350ÿF, in an oven for a period of from about 15 seconds to about 15 minutes, preferably from about 45 seconds to about 3 minutes, to react the formaldehyde with the natural fibers in the fabric and affect crosslinking of the formaldehyde and natural fibers to provide durable press and/or shrinkage resistance effects. There is an inverse relationship between curing temperature and curing time, that is, the higher the temperature of curing, the shorter the dwell time in the oven; conversely, the lower the curing temperature, the longer the dwell time in the oven.
- In another embodiment, the present invention comprises methods for improving the water absorbency of fabric, wherein the silicone elastomer may be included in the treated fabric by means of a separate treatment step before or after the formaldehyde crosslinking treatment. Additionally, if the silicone elastomer or precursor thereof is applied to the fabric subsequent to treatment with the formaldehyde crosslinking composition, the silicone elastomer precursor thereof may be applied prior to or subsequent to the heating step which is employed to affect curing of the formaldehyde with the natural fibers of the fabric, although application prior to heating is preferred. The applied silicone elastomer or precursor thereof may be dried, with self curing of the precursor being affected thereby.
- The fabrics according to the present invention exhibit good water absorbency. As noted above this indicates that the fabrics exhibit a water absorbency time, in accord with the methods described in AATCC Method 79-1995, of less than about 100 seconds. In a more specific embodiment, the fabrics according to the present invention exhibit a water absorbency time, in accord with the methods described in AATCC Method 79-1995, of less than about 80 seconds, even after the fabric has been aqueous laundered at least once. In yet a further embodiment, the fabrics according to the present invention exhibit a water absorbency time, in accord with the methods described in AATCC Method 79-1995, of less than about 60 seconds, even after the fabric has been aqueous laundered at least once. One skilled in the art will appreciate that various fabric preparation processes may involve application of a wetting agent to the fabric. Typically, wetting agents may be employed to improve wet pick-up of chemistry during fabric finishing. The water absorbency properties as disclosed herein are exhibited by the fabric after any such wetting agent has been removed, for example by laundering or the like. Thus, the good water absorbency properties are maintained after one or more washings or launderings of the fabrics. The good water absorbency properties are particularly advantageous when the fabric is used in garment manufacture, as garments which absorb moisture are generally more comfortable for wear and therefore are preferred by consumers over garments which are formed of hydrophobic, non-moisture absorbing fabrics.
- The fabrics according to the invention also exhibit good durable press properties and/or good shrink resistance. In one embodiment, it is preferred that the fabric exhibit good durable press, for example a DP (durable press) rating of at least about 3.0, preferably at least about 3.25, and more preferably at least about 3.5, as measured according to AATCC Test Method 124-1996, after one aqueous washing, more preferably after five aqueous washings, and/or good shrinkage resistance, for example a length shrinkage and a width shrinkage of less than about 10% each, preferably less than about 5% each, more preferably less than about 4% each, and even more preferably less than about 2% each, and in certain embodiments, less than about 1% each, as measured according to AATCC Test Method 135-1995, after one machine washing, more preferably after five aqueous washings. Shrinkage resistance may also be measured according to AATCC Test Method 150-1995. In further preferred embodiments, the fabrics exhibit good filling tensile and tear strengths, for example of at least about 25 pounds and at least about 24 ounces, respectively, as measured according to ASTM D- 5035-95 for tensile strength, and ASTM D-2261-96 for tear strength.
- In another embodiment, cellulose fabrics having a crosslinked formaldehyde treatment and exhibiting good water absorbency, even after laundering, are obtained, provided that the fabric does not comprise 100% cotton. These fabrics may comprise greater than about 20% cotton fibers, greater than about 50% cotton fibers, greater than about 80% cotton fibers, greater than about 20% rayon fibers, greater than about 50% rayon fibers, greater than about 80% rayon fibers, or about 100% rayon fibers.
- In a further embodiment, the fabrics according to the invention exhibit good hand or softness, in the absence of conventional softeners such as silicone or polyethylene softeners. Typically, the fabrics will exhibit a low coefficient of friction and/or a high flexibility/Instron softness.
- In processes in accordance with the present invention, unreacted formaldehyde remaining on the fabric is removed during subsequent processing of the fabric. Generally, the final substrate will comprise less than about 300 ppm formaldehyde, preferably less than about 200 ppm formaldehyde, more preferably less than about 100 ppm formaldehyde, and even more preferably less than about 50 ppm formaldehyde, as measured according to AATCC Test Method 112-1993.
- Some polysiloxanes, generally referred to as silicone oils, have a liquid form, are not elastomeric and do not self-crosslink. Silicone oils include, for example, non-reactive linear polydimethyl siloxanes, that is, siloxanes which are not capable of further reaction with other silicones and are not capable of a self curing reaction. Silicone oils have a tendency to produce non-removable spots on fabrics. In contrast, the silicone elastomers used in the present invention generally do not produce such spots. Although the fabrics or treatment compositions may comprise silicone oil, in one embodiment, the fabrics and treatment compositions are substantially free of, and preferably are free of, silicone oil. As used herein, substantially free of silicone oils means the treatment compositions and fabrics comprise less than 1%, by weight, silicone oil.
- Thermosetting resins used to impart durable press properties to fabrics are generally aminoplast resins which are the products of the reaction of formaldehyde with compounds such as urea, thiourea, ethylene urea, dihydroxyethylene urea and melamines. As used herein “aminoplast resins” is intended to include N-methylolamide cross-linking agents such as dimethylol dihydroxyethylene urea, dimethylol urea, dimethylolethylene urea, dimethylol propylene urea, dimethylol methyl carbamate, dimethylol n-propylcarbamate, dimethylol isopropylcarbamate trimethylolated melamine, and tris(methoxymethol) melamine. Preferably, the fabrics, methods and formaldehyde treatment compositions of the invention are substantially free of, and more preferably are free of, aminoplast resins and N-methylol cross-linking agents. As used herein, “substantially free” of aminoplast resins and N-methylol cross-linking agents is intended to mean the fabrics and treatment solutions comprise less than about 0.5%, by weight, aminoplast resin or methylol cross-linking agent.
- Prior to treatment with the formaldehyde composition and silicone elastomer or precursor thereof, the fabric may optionally be prepared using any fiber, yarn, or textile pre-treatment preparation techniques known in the art. Suitable preparation techniques include brushing, singeing, desizing, scouring, mercerizing, and bleaching. For example, fabric may be treated by brushing which refers to the use of mechanical means for raising surface fibers which will be removed during singeing. The fabric may be then be singed using a flame to burn away fibers and fuzz protruding from the fabric surface. Textiles may be desized, which refers to the removal of sizing chemicals such as starch and/or polyvinyl alcohol, that are put on yarns prior to weaving to protect individual yarns. The fabrics may be scoured, which refers to the process of removing natural impurities such as oils, fats and waxes and synthetic impurities such as mill grease from fabrics. Mercerization refers to the application of high concentrations of sodium hydroxide to a fabric to alter the morphology of fibers, particularly cotton fibers. Fabrics may be mercerized to improve fabric stability and luster. Finally, bleaching refers to the process of destroying any natural color bodies within the natural fiber. A typical bleaching agent is hydrogen peroxide.
- The various preparation techniques are optional and dependent upon the desired final product. For example, when the final fabric is to be dyed a dark color, there may be no need to bleach the substrate. Similarly, there may be no need to desize a knit which was prepared without using any sizing agents, and no need to separately scour knits and woven textiles as the scouring may be done during bleaching.
- The following examples are set forth to demonstrate the methods of the present invention and the good water absorbency which is obtained in fabrics by the methods of the present invention. Throughout the examples and the present specification, parts and percentages are by weight unless otherwise specified. The following examples are illustrative only and are not intended to limit the scope of the methods and fabrics of the invention as defined by the claims.
- In this example, rayon fabric samples are provided with a formaldehyde crosslinking treatment in accordance with the invention. Generally, each fabric is contacted with an aqueous solution comprising about 10% to 20% formalin, a weight ratio of formalin to catalyst solution of about 18:5, and about 3% (solids) of a silicone elastomer commercially available from General Electric under the designation GE SM2112. The aqueous solution is padded on the fabric to provide a moisture content of greater than about 30% and the treated fabric is heated at a temperature greater than about 300° F. for a period of time sufficient to effect crosslinking of the formaldehyde with the cellulose in the rayon fabrics.
- In this example, the water absorbency properties of various fabrics are measured according to AATCC Method 79-1995. Generally, a drop of water is placed on the fabric surface and the time taken for the specular reflection of the drop to disappear is measured as an indication of the water absorbency of the fabric. The shorter the time, the better the water absorbency of the fabric.
- Three fabrics are provided with a formaldehyde crosslinking treatment according to the methods of the invention as described in Example 1 and are subjected to measurement of their water absorbency properties. The first fabric comprises a Tencel® lyocell fabric, the second fabric comprises an 85/15 rayon/flax blend, and the third fabric comprises 100% viscose rayon fabric, all of which are treated generally in accord with the method described in Example 1. An aqueous bath solution comprising about 35% formalin, 10% of a 30% catalyst solution and 5% of a silicone elastomer, Glosil ECR from Glotex Chemical, is employed. The solution further comprises about 1% of a wetting agent. The treated fabrics are cured at about 350ÿF. For comparison purposes, untreated samples of each fabric and samples of each fabric provided with a conventional aminoplast resin and silicone softener combination treatment are also subjected to measurement of their water absorbency properties. The aminoplast treated fabric samples are prepared using a bath solution comprising a conventional aminoplast resin, BF Goodrich Free Res 845 (6%), a conventional cationic fatty amide softener, Fabritone HC (8%), and silicone elastomer/softener, Glosil ECR (2%) from Glotex Chemical. The bath solution further comprises about 1% of a wetting agent.
- The water absorbency of each fabric type is measured initially, before any laundering of the treated or untreated fabric, after one wash cycle at 60° F., after five wash cycles at 60° F., after one wash cycle at 95° F., and after five wash cycles at 95° F. The water absorbency of five samples of each fabric type are measured at the specified conditions and the average of the measured values in seconds is set forth in Table 1, with the standard deviation of the measured values being set forth in parentheses.
TABLE 1 Water Absorbency, Seconds No wash One Wash, Five Washes, One Wash, Five Washes, Fabric Sample cycle 60° F. 60° F. 95° F. 95° F. Tencel ® lyocell, <1 <1 <1 <1 <1 untreated Tencel ® lyocell, 16.8 11.6 3.6 15.5 2.4 formaldehyde treated (3.7) (1.1) (0.5) (3.4) (0.4) Tencel ® lyocell, 4.1 >360 325.8 >360 >360 aminoplast resin treated (0.8) (101.4) Rayon/flax, untreated <1 <1 <1 <1 <1 Rayon/flax, 48.7 70.4 23.6 203.4 57.0 formaldehyde treated (11.7) (17.1) (4.2) (90.6) (9.0) Rayon/flax, aminoplast 10.8 >360 >360 >360 >360 resin treated (2.3) Viscose Rayon, <1 <1 <1 <1 <1 untreated Viscose Rayon, 24.8 65.5 27.9 >360 173.2 formaldehyde treated (5.8) (8.1) (6.3) (67.5) Viscose Rayon, 5.5 >360 >360 >360 >360 aminoplast resin treated (2.0) - As is evident from the results set forth in Table 1, the untreated fabrics all absorb water very rapidly, regardless of the number of washings to which they were subjected. However, these untreated materials are disadvantageous as they do not exhibit good durable press properties and/or good shrinkage resistance and/or, as often in the case of Tencel®, do not exhibit good appearance after laundering. The fabrics treated according to the present methods (formaldehyde treated) all exhibit good water absorbency, both before and after one or more washings. These fabrics are also advantageous in that they exhibit good durable press properties and good shrinkage resistance. Finally, while the aminoplast resin treated fabrics exhibit good water absorbency properties prior to washing, it is believed that this good water absorbency is due to the presence of residual wetting agent from the aqueous resin treatment on the fabric surface. Once the aminoplast resin-treated fabrics are subjected to washing, wherein residual wetting agent is removed, the fabrics exhibit extremely poor water absorbency. One skilled in the art will appreciate that the times of greater than 360 seconds indicate that the fabrics exhibit poor water absorbency.
- In this example, various rayon fabrics are tested for their water absorbency according to AATCC Test Method 79-1995 as described in Example 2. The fabrics are also tested for their durable press properties according to AATCC Test Method 124-1996 after one wash cycle, and for their shrinkage according to AATCC Test Method 135-1995 after one wash cycle. Viscose, modal and lyocell rayon fabrics are tested. The fabric type and treatment chemistry applied to each of rayon fabric samples 1-17 of this example are set forth in Table 2, together with the various test results.
TABLE 2 Water Absorbency, seconds Absorbency, Absorbency, Durable Shrinkage, Rayon no wash 1 wash cycle, Press % warp x % Sample Fabric Treatment Chemistry cycles 95° F. rating fill 1 Viscose Aminoplast resin (15%)1 <1 <1 2.0 3.8 × 1.5 2 Viscose Aminoplast resin (7.5%) <1 <1 1.1 9.4 × 6.0 3 Viscose Aminoplast resin (22%) <1 <1 1.5 2.8 × 1.4 4 Viscose Untreated <1 <1 1.0 10.8 × 7.5 5 Viscose Aminoplast resin (15%) + >270 >300 2.1 3.8 × 3.7 Si softener (3%)2 6 Viscose Aminoplast resin (15%) + <1 <1 2.4 4.1 × 1.6 PE softener (3%)3 7 Viscose Aminoplast resin (15%) + 100 >300 1.9 3.9 × 3.4 Si softener (3%) + PE softener (3%) 8 Viscose Aminoplast resin (15%) + 93 >300 2.5 3.4 × 1.8 Si softener (4.5%) + PE softener (4.5%) 9 Viscose Aminoplast resin (15%) + 70 >300 1.9 3.7 × 1.7 Si softener (6%) + PE softener (6%) 10 Viscose Si softener (3%) + PE >300 >300 2.1 5.2 × 0.9 softener (3%) 11 Viscose Formalin (27.7%) + 12 3.1 0.9 × 0.2 silicone elastomer4 (3%) 12 Viscose Aminoplast resin (15%) + 15 20 2.7 3.4 × 1.8 silicone elastomer (3%) 13 Viscose Aminoplast resin (15%) + 62 67 2.4 3.5 × 2.3 silicone elastomer (3%) + PE softener (3%) 14 Modal Aminoplast resin (15%) + >300 >300 2.7 1.7 × 1.0 Si softener (3%) + PE softener (3%) 15 Modal Formalin (27.7%) + <1 16 4.1 +0.1 × 0.0 silicone elastomer (3%) 16 Lyocell Aminoplast resin (15%) + 88 >300 2.9 0.3 × +0.2 Si softener (3%) + PE softener (3%) 17 Lyocell Formalin (27.7%) + <1 6 3.1 0.2 × 0.1 silicone elastomer (3%) - It will be apparent that samples 11, 15 and 17 are according to the present invention and are treated with both formaldehyde (formalin) and silicone elastomer. Although not specified in Table 2, a catalyst is employed in an approximately 3:1 ratio with the formaldehyde. Water absorbency is tested prior to any washing of the fabric and after one wash cycle conducted at about 95ÿF. As is apparent from Table 2, the rayon fabric samples of samples 11, 15 and 17 according to the invention exhibit excellent water absorbency, particularly after washing, good durable press and good shrinkage resistance.
- With respect to the comparative fabric samples 1- 10, 12-14 and 16, it is important to note that neither the resin treated samples 1-3, 5-9, 12-14 and 16 nor the non-resin-treated samples 4 and 10 exhibit the superior dimensional stability, i.e., shrinkage resistance, which are exhibited by the fabric samples 11, 15 and 17 according to the invention. Similarly, none of the comparative samples 1-10, 12-14, and 16 exhibit the good durable press properties which are exhibited by the fabric samples 11, 15 and 17 according to the invention. Thus, while samples 1-4, 6, 12 and 13 exhibit good water absorbency, these fabrics are unacceptable for consumer use owing to their dimensional instability and/or inferior durable press properties. On the other hand, comparative fabric samples 5, 7-10, 14 and 16 are further unacceptable for consumer use in view of their very poor water absorbency. One skilled in the art will recognize that water absorbency times of greater than about 300 seconds indicate that the fabrics exhibit poor water absorbency. As discussed above, it is believed that the combination of softeners with the aminoplast resin, particularly silicone softeners which are conventionally used to improve the feel of aminoplast resin-treated fabrics, contribute to the poor water absorbency of the fabrics.
- Thus, the advantages of the rayon fabric samples 11, 15 and 17 according to the present invention which exhibit good water absorbency in combination with good dimensional stability, particularly shrink resistance, and good durable press properties are evident.
- The examples and specific embodiments set forth herein are for illustrative purposes only and are not intended to limit the scope of the methods and fabrics of the invention. Additional methods and fabrics within the scope of the claimed invention will be apparent to one of ordinary skill in the art in view of the teachings set forth herein.
Claims (23)
1. A method for providing fabric with good water absorbency and durable press properties, comprising treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde.
2. A method according to claim 1 , wherein the fabric comprises at least about 20% by weight of cotton fibers.
3. A method according to claim 1 , wherein the treatment composition consists essentially of formaldehyde, catalyst and silicone elastomer or a precursor thereof.
4. A method according to claim 1 , wherein the treatment composition is free of aminoplast resin.
5. A method according to claim 1 , wherein the treatment composition comprises a silicone elastomer precursor.
6. A method according to claim 1 , wherein the treated fabric exhibits a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time, a durable press value of at least about 3 after the fabric has been aqueous laundered at least one time, and/or a length shrinkage and a width shrinkage of less than about 5% each after the fabric has been aqueous laundered one time.
7. A method for providing fabric with good water absorbency and shrinkage resistance properties, comprising treating the fabric with a treatment composition comprising formaldehyde, catalyst for crosslinking the formaldehyde with natural fibers in the fabric, and silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde.
8. A method according to claim 7 , wherein the fabric comprises at least about 20% by weight of rayon fibers.
9. A method according to claim 7 , wherein the treatment composition consists essentially of formaldehyde, catalyst and silicone elastomer or a precursor thereof.
10. A method according to claim 7 , wherein the treatment composition is free of aminoplast resin.
11. A method according to claim 7 , wherein the treatment composition comprises a silicone elastomer precursor.
12. A method according to claim 7 , wherein the treated fabric exhibits a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time.
13. A method according to claim 12 , wherein the treated fabric exhibits a length shrinkage and a width shrinkage of less than about 5% each after the fabric has been aqueous laundered at least one time, and/or a durable press value of at least about 3 after the fabric has been aqueous laundered at least one time.
14. A method of providing rayon fabric with reduced shrinkage and good water absorbency, comprising crosslinking cellulose in the fabric with formaldehyde and providing the fabric with a silicone elastomer.
15. A method according to claim 14 , wherein the fabric comprises at least about 50% by weight of rayon fibers.
16. A method according to claim 14 , wherein the treated fabric exhibits a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time.
17. A method according to claim 16 , wherein the treated fabric exhibits a length shrinkage and a width shrinkage of less than about 5% each after the fabric has been aqueous laundered at least one time.
18. A method according to claim 17 , wherein the treated fabric exhibits a durable press value of at least about 3 after the fabric has been aqueous laundered at least one time.
19. Fabric comprising rayon fibers and exhibiting a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time.
20. Fabric according to claim 19 , wherein the treated fabric exhibits a length shrinkage and a width shrinkage of less than about 5% each after the fabric has been aqueous laundered at least one time.
21. Fabric according to claim 20 , wherein the treated fabric exhibits a durable press value of at least about 3 after the fabric has been aqueous laundered at least one time.
22. Fabric comprising cotton fibers, having a crosslinked formaldehyde durable press treatment, provided with a silicone elastomer, and exhibiting a water absorbency time of less than about 100 seconds as measured according to AATCC Method 79-1995 after the fabric has been aqueous laundered at least one time, wherein the fabric does not comprise 100% cotton.
23. A method for providing fabric with good water absorbency and at least one of durable press properties and shrinkage resistance, comprising treating the fabric with a treatment composition comprising formaldehyde and catalyst for crosslinking the formaldehyde with natural fibers in the fabric, treating the fabric with silicone elastomer or a precursor thereof, and heating the treated fabric to effect crosslinking of the formaldehyde.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/821,313 US20020031970A1 (en) | 2000-03-29 | 2001-03-29 | Methods for improving water absorbency of fabrics and fabrics with improved properties |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US19290300P | 2000-03-29 | 2000-03-29 | |
US09/821,313 US20020031970A1 (en) | 2000-03-29 | 2001-03-29 | Methods for improving water absorbency of fabrics and fabrics with improved properties |
Publications (1)
Publication Number | Publication Date |
---|---|
US20020031970A1 true US20020031970A1 (en) | 2002-03-14 |
Family
ID=22711495
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US09/821,313 Abandoned US20020031970A1 (en) | 2000-03-29 | 2001-03-29 | Methods for improving water absorbency of fabrics and fabrics with improved properties |
Country Status (4)
Country | Link |
---|---|
US (1) | US20020031970A1 (en) |
EP (1) | EP1278905A2 (en) |
AU (1) | AU2001249630A1 (en) |
WO (1) | WO2001073184A2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6528438B2 (en) * | 1997-05-13 | 2003-03-04 | The Procter & Gamble Company | Durable press/wrinkle-free process |
US7214652B1 (en) * | 2005-12-30 | 2007-05-08 | 3M Innovative Properties Company | Anionic surfactant-containing hypochlorite bleach composition and methods of making and use |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003106756A2 (en) * | 2002-06-17 | 2003-12-24 | The Procter & Gamble Company | Methods for improving dimensional stability and/or durable press properties of elastic fabrics and elastic fabrics with improved properties |
AT511186A1 (en) * | 2011-03-01 | 2012-09-15 | Chemiefaser Lenzing Ag | Shrink-resistant and industrially washable fabrics made of viscose and modal fibers with particulate additives |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL286002A (en) * | 1961-11-28 | |||
US3420696A (en) * | 1964-06-02 | 1969-01-07 | West Point Pepperell Inc | Aldehyde fixation on polymeric material |
US5885303A (en) * | 1997-05-13 | 1999-03-23 | American Laundry Machinery Incorporated | Durable press/wrinkle-free process |
ES2330978T3 (en) * | 1998-05-11 | 2009-12-17 | Strike Investments, Llc | PROCEDURE THAT ALLOWS YOU TO OBTAIN A WRINKLESS FABRIC WITHOUT FOLDINGS. |
-
2001
- 2001-03-29 WO PCT/US2001/010203 patent/WO2001073184A2/en not_active Application Discontinuation
- 2001-03-29 EP EP01922877A patent/EP1278905A2/en not_active Withdrawn
- 2001-03-29 US US09/821,313 patent/US20020031970A1/en not_active Abandoned
- 2001-03-29 AU AU2001249630A patent/AU2001249630A1/en not_active Abandoned
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6528438B2 (en) * | 1997-05-13 | 2003-03-04 | The Procter & Gamble Company | Durable press/wrinkle-free process |
US7214652B1 (en) * | 2005-12-30 | 2007-05-08 | 3M Innovative Properties Company | Anionic surfactant-containing hypochlorite bleach composition and methods of making and use |
Also Published As
Publication number | Publication date |
---|---|
WO2001073184A2 (en) | 2001-10-04 |
AU2001249630A1 (en) | 2001-10-08 |
WO2001073184A3 (en) | 2002-01-31 |
EP1278905A2 (en) | 2003-01-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6565612B2 (en) | Shrink resistant rayon fabrics | |
US20060037150A1 (en) | Compositions and methods for treating textiles to impart wrinkle resistance, softness and hydrophilicity | |
US6716255B2 (en) | Textile finishing process | |
US20040068802A1 (en) | Methods for improving dimensional stability and/or durable press properties of elastic fabrics and elastic fabrics with improved properties | |
US20010049247A1 (en) | Methods for reducing fabric drying time and fabrics with improved properties | |
US5296269A (en) | Process for increasing the crease resistance of silk textiles | |
AU2005267424B2 (en) | Stretch fabrics with wrinkle resistance | |
WO2000019003A1 (en) | Textile finishing process | |
US20020031970A1 (en) | Methods for improving water absorbency of fabrics and fabrics with improved properties | |
US6673125B2 (en) | Chemically modified nonwoven articles and method for producing the same | |
US20010051486A1 (en) | Methods for improving fibrillation or pill resistance of fabrics and fabrics with improved properties | |
EP1274894A2 (en) | Methods for improving fibrillation or pill resistance of fabrics and fabrics with improved properties | |
JP4198597B2 (en) | Permanent press processing of fabric | |
US6602437B1 (en) | Chemically modified nonwoven articles and method for producing the same | |
GB2360795A (en) | Anionically dyeable, durable press, natural fibre products | |
US20020049019A1 (en) | Methods for improving brightness of fabrics and fabrics of improved brightness | |
JP2000192371A (en) | Fabric containing cellulosic fiber | |
US20030157854A1 (en) | Chemically modified nonwoven articles and method for producing the same | |
WO2022144823A1 (en) | Fabric finishing process | |
JPH0770930A (en) | Method for processing purified cellulose fiber cloth | |
JPH07268774A (en) | Processing method of cellulosic fiber | |
JPH04352867A (en) | Modification of cellulosic fiber | |
WO2003066959A1 (en) | Chemically modified nonwoven articles and method for producing the same | |
JPH0849168A (en) | Production of crease-resistant textile fabric |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |