US2592852A - Process of producing dyed lustrous printed pattern effects using acidcuring resins and free leuco bases of vat dyes - Google Patents
Process of producing dyed lustrous printed pattern effects using acidcuring resins and free leuco bases of vat dyes Download PDFInfo
- Publication number
- US2592852A US2592852A US20114A US2011448A US2592852A US 2592852 A US2592852 A US 2592852A US 20114 A US20114 A US 20114A US 2011448 A US2011448 A US 2011448A US 2592852 A US2592852 A US 2592852A
- Authority
- US
- United States
- Prior art keywords
- fabric
- printing
- lustrous
- paste
- printed
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title claims description 16
- 229920005989 resin Polymers 0.000 title claims description 12
- 239000011347 resin Substances 0.000 title claims description 12
- 230000000694 effects Effects 0.000 title claims description 10
- 239000000984 vat dye Substances 0.000 title description 7
- 239000004744 fabric Substances 0.000 claims description 70
- 238000007639 printing Methods 0.000 claims description 53
- 239000000975 dye Substances 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 16
- 239000004753 textile Substances 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 9
- 239000001913 cellulose Substances 0.000 claims description 7
- 229920002678 cellulose Polymers 0.000 claims description 7
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 238000010002 mechanical finishing Methods 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 19
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
- 239000000243 solution Substances 0.000 description 15
- 239000006185 dispersion Substances 0.000 description 11
- 238000011282 treatment Methods 0.000 description 11
- ZHXAZZQXWJJBHA-UHFFFAOYSA-N triphenylbismuthane Chemical compound C1=CC=CC=C1[Bi](C=1C=CC=CC=1)C1=CC=CC=C1 ZHXAZZQXWJJBHA-UHFFFAOYSA-N 0.000 description 11
- 238000005406 washing Methods 0.000 description 11
- 239000002585 base Substances 0.000 description 10
- 239000000314 lubricant Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- SOIFLUNRINLCBN-UHFFFAOYSA-N ammonium thiocyanate Chemical compound [NH4+].[S-]C#N SOIFLUNRINLCBN-UHFFFAOYSA-N 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 235000011121 sodium hydroxide Nutrition 0.000 description 6
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
- 239000000049 pigment Substances 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 229920001807 Urea-formaldehyde Polymers 0.000 description 4
- 238000003490 calendering Methods 0.000 description 4
- -1 kelgin gums Polymers 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000005696 Diammonium phosphate Substances 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical group [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- 230000032683 aging Effects 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 3
- 229910000388 diammonium phosphate Inorganic materials 0.000 description 3
- 235000019838 diammonium phosphate Nutrition 0.000 description 3
- NXYNTHCSPIVNNX-SAIUNTKASA-N leucoester Natural products CCCCCCCCCCCCCCCC(=CCOC(=O)CCC[C@H](C)CCC[C@H](C)CCC(C)C)C NXYNTHCSPIVNNX-SAIUNTKASA-N 0.000 description 3
- 239000012260 resinous material Substances 0.000 description 3
- 235000010288 sodium nitrite Nutrition 0.000 description 3
- 235000019698 starch Nutrition 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 3
- PUMIBBNWDCWIKR-UHFFFAOYSA-M 1-(octadecoxymethyl)pyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCOC[N+]1=CC=CC=C1 PUMIBBNWDCWIKR-UHFFFAOYSA-M 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 229920003043 Cellulose fiber Polymers 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 229930194542 Keto Natural products 0.000 description 2
- 229920000161 Locust bean gum Polymers 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical group [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 2
- 150000004056 anthraquinones Chemical class 0.000 description 2
- 230000001055 chewing effect Effects 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical compound OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 2
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 2
- 235000019239 indanthrene blue RS Nutrition 0.000 description 2
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 125000000468 ketone group Chemical group 0.000 description 2
- 239000004310 lactic acid Substances 0.000 description 2
- 235000014655 lactic acid Nutrition 0.000 description 2
- 239000000711 locust bean gum Substances 0.000 description 2
- 235000010420 locust bean gum Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- ADABARLJFURQEM-UHFFFAOYSA-N n-(1-methylpyridin-1-ium-2-yl)octadecanamide;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC(=O)NC1=CC=CC=[N+]1C ADABARLJFURQEM-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 2
- KMUONIBRACKNSN-UHFFFAOYSA-N potassium dichromate Chemical compound [K+].[K+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KMUONIBRACKNSN-UHFFFAOYSA-N 0.000 description 2
- PUNUCLJJWUUKFB-UHFFFAOYSA-N s-ethyl n-cyclohexylcarbamothioate Chemical compound CCSC(=O)NC1CCCCC1 PUNUCLJJWUUKFB-UHFFFAOYSA-N 0.000 description 2
- 238000004513 sizing Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- BFHKYHMIVDBCPC-UHFFFAOYSA-N 1,3,5,7-tetrahydro-[1,3]oxazolo[3,4-c][1,3]oxazol-7a-ylmethanol Chemical compound C1OCN2COCC21CO BFHKYHMIVDBCPC-UHFFFAOYSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 235000013912 Ceratonia siliqua Nutrition 0.000 description 1
- 240000008886 Ceratonia siliqua Species 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-N Formic acid Chemical compound OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229920000569 Gum karaya Polymers 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 241000934878 Sterculia Species 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XHRCTKFMKIDXSH-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)-methylamino]methanol Chemical compound OCN(C)C1=NC(N)=NC(N)=N1 XHRCTKFMKIDXSH-UHFFFAOYSA-N 0.000 description 1
- HBJUDHILVBLZJL-UHFFFAOYSA-L [Na+].[Na+].O=C.[O-]S(=O)S([O-])=O Chemical compound [Na+].[Na+].O=C.[O-]S(=O)S([O-])=O HBJUDHILVBLZJL-UHFFFAOYSA-L 0.000 description 1
- 150000001243 acetic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000019270 ammonium chloride Nutrition 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
- 239000010775 animal oil Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005108 dry cleaning Methods 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 150000004674 formic acids Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000009432 framing Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 235000001727 glucose Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940015043 glyoxal Drugs 0.000 description 1
- IZVTZBGKNGTXDR-UHFFFAOYSA-N hydrogen phosphate;2-hydroxyethylazanium Chemical compound [NH3+]CCO.[NH3+]CCO.OP([O-])([O-])=O IZVTZBGKNGTXDR-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 239000012182 japan wax Substances 0.000 description 1
- 239000000231 karaya gum Substances 0.000 description 1
- 235000010494 karaya gum Nutrition 0.000 description 1
- 229940039371 karaya gum Drugs 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- QTWZICCBKBYHDM-UHFFFAOYSA-N leucomethylene blue Chemical compound C1=C(N(C)C)C=C2SC3=CC(N(C)C)=CC=C3NC2=C1 QTWZICCBKBYHDM-UHFFFAOYSA-N 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000010297 mechanical methods and process Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- ITFGZZGYXVHOOU-UHFFFAOYSA-N n,n-dimethylmethanamine;methyl hydrogen sulfate Chemical compound C[NH+](C)C.COS([O-])(=O)=O ITFGZZGYXVHOOU-UHFFFAOYSA-N 0.000 description 1
- URXNVXOMQQCBHS-UHFFFAOYSA-N naphthalene;sodium Chemical compound [Na].C1=CC=CC2=CC=CC=C21 URXNVXOMQQCBHS-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 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
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical group [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 239000001488 sodium phosphate Chemical group 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- HVTHJRMZXBWFNE-UHFFFAOYSA-J sodium zincate Chemical compound [OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Zn+2] HVTHJRMZXBWFNE-UHFFFAOYSA-J 0.000 description 1
- HLPHHOLZSKWDAK-UHFFFAOYSA-M sodium;formaldehyde;naphthalene-1-sulfonate Chemical compound [Na+].O=C.C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HLPHHOLZSKWDAK-UHFFFAOYSA-M 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000003351 stiffener Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical group [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06Q—DECORATING TEXTILES
- D06Q1/00—Decorating textiles
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06Q—DECORATING TEXTILES
- D06Q1/00—Decorating textiles
- D06Q1/08—Decorating textiles by fixation of mechanical effects, e.g. calendering, embossing or Chintz effects, using chemical means
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile
Definitions
- This invention relates to. dyed durable lustrous printed, pattern effects for cellulose textile fabrics.
- the primary object of the present invention is to provide a process whereby vat dyes may be incorporated in the resinous printing paste and sharp, distinct, colored, lustrous mechanical finished patterns may be obtained having excel lent light and wash fastness and without smearing and mark-oil? of the pattern on the unprinted portion of the cloth.
- vat type of dye it is especially valuable to be able to use a vat type of dye since this type allows a complete and full range of colors of a high degree of durability to light and washing, and exceptionally good and durable results are obtained with, the better grades of anthraquinone and thio-indigo types which are recommended for this process.
- dyes come on the market in pigment form, i. e., they are in particle form, each particle containing thousands of dye molecules.
- the dyestufl has no aflinity for the cellulose fibers and if printed upon the fabric, will mark-01f in the glazer and bleed and wash oif during subsequent washing.
- vat dye or dyes are first treated in an alkaline solution containing a reducing agent, usually caustic soda and sodium hydrosulfite which will reduce the dyestuff" into what is called the leuco form underwhich conditions the dyestuff is obtained in the solution in the molecular or semi-molecular form as the sodium salt of the leuco base of the dyestuff.
- a reducing agent usually caustic soda and sodium hydrosulfite
- Dispersing agents such as- Blancol (sodium naphthalene sulfonate-formaldehyde) may also be added to aid the dispersion.
- the solution containing the leuco base is now mixed into the printing paste containing the usual type of printing gum or mixtures of printing gums such as, for example, starch, converted starch, gum tragacanth, karaya gum, locust bean gum, kelgin gums, methyl cellulose polymerized styrene gum, and acrylate gum.
- printing gums such as, for example, starch, converted starch, gum tragacanth, karaya gum, locust bean gum, kelgin gums, methyl cellulose polymerized styrene gum, and acrylate gum.
- Any well known printing gum may be used provided it does not undesirably alter the state of the dyestuif nor interfere with the setting of the resinous material used.
- Theprinting paste also contains the thermosetting resin forming ingredients which may be, for example, melamine-formaldehyde, phenolformaldehyde, urea-formaldehyde, dicyandiamide-formaldehyde, urea-glyoxal, and mixtures of melamine-formaldehyde, and urea-formaldehyde.
- thermosetting resin forming ingredients may be, for example, melamine-formaldehyde, phenolformaldehyde, urea-formaldehyde, dicyandiamide-formaldehyde, urea-glyoxal, and mixtures of melamine-formaldehyde, and urea-formaldehyde.
- thermo-setting resin serve as the printing gum by using, for example, polyvinyl alcohol-formaldehyde, methyl celluloseglyoxal, or starch-formaldehyde thermo-sctting materials. These products while serving as the resin forming material also have enough viscosity in solution to serve as the printing gum. Usually, under these conditions, a stiffer print is obtained and this is somewhat desirable.
- a catalyst may be dispensed with, but usually it is found advantageous to add a catalyst to speed the setting of the thermo-setting materials.
- the usual type of catalysts such as, for example, diammonium phosphate, ammonium 'thiocyanate, di-monoethanolamine phosphate, ammonium sulfate, and di-propanolamine phosphate, may be employed. Catalysts should preferably not be used which would precipitate the dyestuif.
- Similar printing pastes as the ones described above may be prepared using the leuco ester type of vat dyes sold on the market under the commercial names of Algosol and Indigosol. Since these leuco ester compounds of the vat dyestuff form molecular dispersions when added to water, it is possible to add these directly to the printing gum containing the thermosetting resin catalyst and lubricant together with an acid such as lactic, acetic, and sulphuric, and a mild oxidizing agent such as sodium nitrite; these latter serving to change the leuco ester dyestuff into a molecular or semi-molecular dispersion of the vat dyestuff during the processing which is identical with the procedure already described for the regular type of vat dyestuff.
- an acid such as lactic, acetic, and sulphuric
- a mild oxidizing agent such as sodium nitrite
- the printing paste may also contain a lubricant to prevent the sticking and chewing of the cloth when passing through the mechanical equipment. This addition becomes necessary when large printed patterns are glazed as these would not go through the glazer without some lubrication.
- Sulfonated vegetable, petroleum, and animal oil may be used but care should be taken that these products do not flocculate or coagulate the leuco base vat dye dispersion when added to the printing paste as this will be detrimental.
- Lubricants of a permanent character which have a tendency to remain in the print after the final washing may also be used; these will act as softeners in the finished fabric and may also impart water resistance which is sometimes desirable when the fabric is subsequently to be overdyed as will be further explained.
- durable lubricants we may mention cation-active softeners, such as, for example, Triton K-GO (tetra alkyl quaternary ammonium chloride), Amonyx T (trialkylbenzyl ammonium chloride), stearamidomethylpyridinium chloride, and stearyloxymethylpyridinium chloride. The last two products will also impart water resistance to the finished printed pattern.
- the fabric is printed in a customary manner, the number of printing rolls employed corresponding to the number of different colors in the pattern.
- the printing may also be done by means of the system known as screen printing instead of on one of the regular types of printing machines.
- the cloth After printing, the cloth is carefully dried until the printed portion of the fabric Preferably contains from 5% to 15% moisture by weight of the fabric above that of the normal moisture content of the fabric. After the cloth has been dried, it may be advantageously cooled by passing it either through a cooling chamber or over cooling cans.
- the printed portion containing the thermo-setting material will, after curing, be durable to the subsequent washing treatment and the mechanical finish will remain, resulting in a two-tone effect between the printed and the unprinted portion, showing a high glossy print against a durable background.
- the heated bowls on the friction calender are operated between 300 F. and 400 F., polymerization will occur on the calender, and if a sufiicient number of runs are given, the polymerization of the resinous material may actually be completed thereon. In case the polymerization is not completed on the calender, it is advantageous to give the fabric a short cure at elevated temperature to complete the setting.
- the heated steel bowl has the higher surface speed.
- calenders imparting mechanical finishes to textile fabrics may also be used.
- the chase and flat nip calenders we prefer to operate at a temperature of from approximately 200 F. to 300 F. on heated bowls.
- the schreiner and embossing calenders we prefer to operate between the temperatures of approximately 200 F. to 400 F.
- the curing of the resin depends to some extent upon the previous treatment the cloth has received. As stated above, it is possible to completely cure the fabric by multiple runs on a calender operating at high temperatures. When operating at the lower temperatures using two or perhaps three runs, it is preferable to cure the fabric in an oven at a temperature ranging from 250 F. to 400 F., and a period of time rangin from 10 minutes to 1 minute. In the case of the chaser and the fiat nip calender, we prefer to cure the fabric in an oven at a temperature ranging from about 250 F. to about 400 F., for a period of time ranging from about 15 minutes to about 2 minutes.
- Thatthe pattern does not mark off even when using a hot friction calender, we attribute to. the fact that the d'yestuifis. present inthe printing paste primarily in a molecular or semi-molecular form rather than in large pigment particle form, so that when printed and partly dried, the. dyestuif penetrates and adheres to the fabric. and stays there during the calendering rather than sticking on the hot bowl and then marking off on the cloth.
- the same dyestufi as sold in pigment form is added to the same printing paste, printed; dried, and calendered, it will. be found to smear and mark-on" within a few yards.
- vat dyestufi after printing and before calenderingsince such treatment would smear the pattern.
- the usual steam aging method of developing vat prints cannot be used prior to calendering since the steam aging sets up the resinous material, resulting in a non-durable mechanical finish.
- To develop the dyestufi after calendering and curing is also impractical since the strong chemical treatments at elevated temperatures necessary to develop the dyes will either destroy or seriously reduce the mechanical finish.
- the cured fabric may be run through an oxidizing solution to insure complete conversion of the leuco dyestuff to. the. keto. or insoluble. form.
- an oxidizing solution for example, hydrogen peroxide, sodium perborate, and potassium dichromate may be used. This step, however, is not necessary since ithas. been found that the contact with the air during printing, drying, and curing, has for all practical purposes already converted the dyestuif to the keto or insoluble form.
- caustic soda and sodium. hydrosulphite to reduce and disperse the vat. dyestufi
- the caustic soda may be substituted by potassium hydroxide, trisodium phosphate, soda ash, triethanolamine, and other strong alkalies.
- the hydrosulphite maybe substituted by sodium sulfoxylate formaldehyde, sodium ibisulphi-te, sodium hydrosulphite formaldehyde, and others.
- sodium liydrosulphite and caustic soda are used in proportions which vary according to dyestulf but which are well known in the art.
- thermo-setting material in the printing may be varied between wide limits, depending upon the degree of stillnessv desired in the printed. portion.
- the latter may vary between a softflexible print. approaching the unprinted part of the cloth. in hand to a firm stifi pattern imposed upon a soft flexible background of unprinted cloth.
- we. operate. between 6% thermosetting materialin the printin gum to 25% by weight of the paste.
- the percentage of dyestuir' may also be varied. It is, of course, rather difiicult: to give a: lower limit since. the printing; paste may be applied: in the tinted form, in. which case. only a very small quantity of dyestuif is used, say .l% by weight of the paste.
- the upper limit on the percentage of dyestuif varies, depending upon the ease with which a dyestuif will. mark. ofi during the mechanical processing and. also upon many other factors, such as percentage of moisture in the printybefore the; mechanical: treatmenitis; applied. type of gum, lubricant, and other ingredients.
- the patterns. represent approximately 80% coverage
- no difficulty is encountered in passing the fabric through the friction calender.
- the friction calender if the coverage is substantially less, than 80%, then it is desirable, in order to prevent chewing of the fabric, to size the fabric before printing with a sizing producing. substantially the. same coefiicient of friction as the printed areas after printing.
- the sizing solution should contain a small percentage of the lubricants mentioned previously, usually about 10% by weight, and may in addition also contain a small percentage of some stiffening agent such as, for example, dextrin, casein, glucose, and starch.
- the fabric after curing or after washing and drying may be subjected to further auxiliary textile treatments to produce new and novel effects.
- a sheer lawn having the lustrous colored patterns applied may be subjected to cellulose swelling treatments such as, for example, treatments with cuprammonium solutions and caustic sodium zincate solutions to produce organdy effects, the final results. being alustrous colored pattern on a sheer organdy fabric.
- Example I The printing paste was made by first preparing the molecular or the very fine dispersion of the vat" dye-stuff. The following formula was used to prepare this dispersion:
- a 40", 48/48, 3.50, cotton fabric which had previously been purified through the regular bleaching process was printed by passing it through a regular textile printing machine followed by careful drying, so that approximately 10% moisture above the normal moisture remained in the printed portion of the cloth.
- the cloth was then taken to a conventional friction calender having a friction ratio of 3:1, a total pressure of 40 tons, and a temperature of the upper steel bowl of approximately 350 F. The cloth was given three runs through this calender and during this procedure, no mark-off, smearing, or staining of the unprinted portion of the cloth took place.
- Example If A dispersion of reduced vat dyestuff was prepared as described in Example I, except that Ponsol Violet BN Paste (C. I. 1163) was used as the dyestuff.
- the printing paste used in'this case had the following composition:
- a 40", 46/40, 3.50, spun rayon fabric was presized by padding it through a solution containing dextrine and /2% sulphonated tallow by weight and then framing to width.
- the cloth so prepared was printed in the regular printing machine, using the conventional methods of printing and using the printing pastes described above.
- the cloth after printing was carefully dried until approximately 10% of residual moisture above the normal moisture remained in the printed portions of the fabric.
- This fabric was then passed once through a 5-bowl heavyweight chasing calender, using a temperature of 300 F. on the heated bowls and a total pressure of 30 tons on the machine.
- the cloth was then washed through a warm solution containing a small quantity of detergent and alkaline material, followed by a thorough washing in warm water.
- the fabric was then extracted and frame dried.
- the resulting cloth had a mellow, deep-seated lustrous, colored pattern imposed upon a dull white background of unprinted cloth. This eifect was durable to drycleaning, soaping, treatments, and light.
- Example III Dispersion of the leuco base was prepared as previously described, using the following formulation:
- a printing paste having the following composition was prepared:
- Example IV A four-color lustrous printed pattern on a dull dyed fabric was obtained.
- Example V A printing paste of the following composition was made up:
- Algosol Green lBW Paste (C. I. 1101) 75 Carbowax 1500 1000 Lactic acid (85%) 100 Ammonium thiocyanate 120 Aerotex M-3 2000 Sodium nitrite 150 Supertex T-125 4000 Water 2400 Color was pasted with small amount of water, added to Supertex T125, and mixed thoroughly. Sodium nitrite, Aerotex M-3, and Carbowax 1500, put into solution and added in order. Finally, the lactic acid (85%) and ammonium thiocyanate in water solution were added and the total mixture was strained. Printing and processing was carried out as described in Example I.
- An aqueous printing paste for use in producing durable mechanical colored lustrous pattern effects on cellulose textile fabrics which tern efiects on cellulose textile fabrics, which consists essentially of Water, printing gum, vat dyestuff in free leuco base form, thermosetting acid-curing resin-forming materials, an acidic catalyst, and a softener.
- a printing paste according to claim 5 in which a textile lubricant is employed in addition to a textile softener.
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Description
Patented Apr. 15, 1952 PROCESS OF PRODUCING DYED LUSTROUS PRINTED PATTERN EFFECTS USING ACID- CURING. RESINS AND FREE LEUCO BASES OF VAT DYES George Alan Billingsley, Jr., and William P. Hall, Wilmington, Del., assignors to Joseph Bancroft & Sons 00., Wilmington, DeL, a corporation of Delaware No Drawing. Application April 9, 1948,
Serial No. 20,114
9 Claims.
This invention relates to. dyed durable lustrous printed, pattern effects for cellulose textile fabrics.
It has. been known how to produce clear, undyed (lustrous) pattern effects by printing a pattern with, a clear (containing no dyestufl") paste embodying thermo-setting resin-forming materials'which become water insoluble when heated. The thus printed fabric is then passed through a heated calender, such as a friction calender, onkwhich the resin is wholly or partially polymerized. In the latter case, the fabric is then passed through an oven to complete the polymerization.
It hasv also been known how to introduce naphthol dyes into a lustrous (and other mechanical methods) pattern, by adding the naphthol base to the unprinted cloth and then to print with a resin-printing gum mixture containing the naphthol salt. This method, although a valuable method, has the drawback of limitation of the number of durable colors obtainable on a practical scale since a given naphthol base treated cloth can only produce a few colors (sometimes only one) of good durability. Besides the naphthol range of colors are quite limited, being primarily valuable in producing red, yellow, and orange colors.
Heretoiore, it has been impossible to incorporate pigments in the printing paste and obtain a commercially practical process. This is due to the fact that when the moist printed pattern is passed through the mechanical finishing equipment, the pigmented printed pattern will mark-ofi on the hot bowls of the calenders which again will transfer the color to the cloth resulting in mark-01f. In the case of a mechanical machine such as a friction calender which operates at high temperature, this difiiculty becomes so serious after a few yards have been run that the calender actually becomes a printing machine.
The primary object of the present invention is to provide a process whereby vat dyes may be incorporated in the resinous printing paste and sharp, distinct, colored, lustrous mechanical finished patterns may be obtained having excel lent light and wash fastness and without smearing and mark-oil? of the pattern on the unprinted portion of the cloth.
It is especially valuable to be able to use a vat type of dye since this type allows a complete and full range of colors of a high degree of durability to light and washing, and exceptionally good and durable results are obtained with, the better grades of anthraquinone and thio-indigo types which are recommended for this process.
These particular dyes" come on the market in pigment form, i. e., they are in particle form, each particle containing thousands of dye molecules. In this form the dyestufl has no aflinity for the cellulose fibers and if printed upon the fabric, will mark-01f in the glazer and bleed and wash oif during subsequent washing.
To obtain the desired results, we proceed as follows:
The above vat dye or dyes are first treated in an alkaline solution containing a reducing agent, usually caustic soda and sodium hydrosulfite which will reduce the dyestuff" into what is called the leuco form underwhich conditions the dyestuff is obtained in the solution in the molecular or semi-molecular form as the sodium salt of the leuco base of the dyestuff. Dispersing agents such as- Blancol (sodium naphthalene sulfonate-formaldehyde) may also be added to aid the dispersion.
This.- alkaline solution is then carefully neutralized with an acid material preferably formic or acetic acids, until the solution is about neutral or slightly acid. Under these conditions, primarily the free leuco base of the dyestuif is obtained which, although it has less affinity for cellulose than the sodium leuco base of the dyestuff, still has a greater aflinity for the cellulose fiber and penetrates more readily than the large size pigment particles of the dyestuif as supplied.
The solution containing the leuco base is now mixed into the printing paste containing the usual type of printing gum or mixtures of printing gums such as, for example, starch, converted starch, gum tragacanth, karaya gum, locust bean gum, kelgin gums, methyl cellulose polymerized styrene gum, and acrylate gum. Any well known printing gum may be used provided it does not undesirably alter the state of the dyestuif nor interfere with the setting of the resinous material used.
Theprinting paste also contains the thermosetting resin forming ingredients which may be, for example, melamine-formaldehyde, phenolformaldehyde, urea-formaldehyde, dicyandiamide-formaldehyde, urea-glyoxal, and mixtures of melamine-formaldehyde, and urea-formaldehyde.
It is possible to have the thermo-setting resin serve as the printing gum by using, for example, polyvinyl alcohol-formaldehyde, methyl celluloseglyoxal, or starch-formaldehyde thermo-sctting materials. These products while serving as the resin forming material also have enough viscosity in solution to serve as the printing gum. Usually, under these conditions, a stiffer print is obtained and this is somewhat desirable.
If the printing paste is sufficiently acid, the use of a catalyst may be dispensed with, but usually it is found advantageous to add a catalyst to speed the setting of the thermo-setting materials. The usual type of catalysts such as, for example, diammonium phosphate, ammonium 'thiocyanate, di-monoethanolamine phosphate, ammonium sulfate, and di-propanolamine phosphate, may be employed. Catalysts should preferably not be used which would precipitate the dyestuif.
Similar printing pastes as the ones described above may be prepared using the leuco ester type of vat dyes sold on the market under the commercial names of Algosol and Indigosol. Since these leuco ester compounds of the vat dyestuff form molecular dispersions when added to water, it is possible to add these directly to the printing gum containing the thermosetting resin catalyst and lubricant together with an acid such as lactic, acetic, and sulphuric, and a mild oxidizing agent such as sodium nitrite; these latter serving to change the leuco ester dyestuff into a molecular or semi-molecular dispersion of the vat dyestuff during the processing which is identical with the procedure already described for the regular type of vat dyestuff.
The printing paste may also contain a lubricant to prevent the sticking and chewing of the cloth when passing through the mechanical equipment. This addition becomes necessary when large printed patterns are glazed as these would not go through the glazer without some lubrication. Sulfonated vegetable, petroleum, and animal oil may be used but care should be taken that these products do not flocculate or coagulate the leuco base vat dye dispersion when added to the printing paste as this will be detrimental. We prefer to use such products as polymerized ethylene oxide (Carbowaxes), lecithin, fatty chain modified melamine resin products (Aerotex Softener H), or emulsion of waxes or oil such as Japan wax, carnauba wax, and castor oil.
Lubricants of a permanent character which have a tendency to remain in the print after the final washing may also be used; these will act as softeners in the finished fabric and may also impart water resistance which is sometimes desirable when the fabric is subsequently to be overdyed as will be further explained. Among durable lubricants we may mention cation-active softeners, such as, for example, Triton K-GO (tetra alkyl quaternary ammonium chloride), Amonyx T (trialkylbenzyl ammonium chloride), stearamidomethylpyridinium chloride, and stearyloxymethylpyridinium chloride. The last two products will also impart water resistance to the finished printed pattern.
When the printing paste or pastes has or have been prepared, the fabric is printed in a customary manner, the number of printing rolls employed corresponding to the number of different colors in the pattern. The printing may also be done by means of the system known as screen printing instead of on one of the regular types of printing machines.
After printing, the cloth is carefully dried until the printed portion of the fabric Preferably contains from 5% to 15% moisture by weight of the fabric above that of the normal moisture content of the fabric. After the cloth has been dried, it may be advantageously cooled by passing it either through a cooling chamber or over cooling cans.
In the case of friction calender finish, the dried fabric is now passed through the friction calender, usually about three times. In the friction calender which exerts high pressure and friction on the fabric at elevated temperatures, the fabric is physically deformed so that a smooth, high-polished product is obtained. This glossy effect is produced over the entire fabric, but will only have a durable character where the fabric was printed, and during the subsequent washing after curing, the fibers and yarns in the unprinted portion will loosen or swell and destroy the mechanical finish, giving a dull eifect. 0n the other hand, the printed portion containing the thermo-setting material will, after curing, be durable to the subsequent washing treatment and the mechanical finish will remain, resulting in a two-tone effect between the printed and the unprinted portion, showing a high glossy print against a durable background.
If the heated bowls on the friction calender are operated between 300 F. and 400 F., polymerization will occur on the calender, and if a sufiicient number of runs are given, the polymerization of the resinous material may actually be completed thereon. In case the polymerization is not completed on the calender, it is advantageous to give the fabric a short cure at elevated temperature to complete the setting. We prefer to operate the calender at high pressure (40 ton total pressure) and with a friction ratio of from about 1 /2 to 1 to about 3 to 1. The heated steel bowl has the higher surface speed.
Other calenders imparting mechanical finishes to textile fabrics may also be used. In the case of the chase and flat nip calenders, we prefer to operate at a temperature of from approximately 200 F. to 300 F. on heated bowls. In the case of the schreiner and embossing calenders, we prefer to operate between the temperatures of approximately 200 F. to 400 F.
The curing of the resin depends to some extent upon the previous treatment the cloth has received. As stated above, it is possible to completely cure the fabric by multiple runs on a calender operating at high temperatures. When operating at the lower temperatures using two or perhaps three runs, it is preferable to cure the fabric in an oven at a temperature ranging from 250 F. to 400 F., and a period of time rangin from 10 minutes to 1 minute. In the case of the chaser and the fiat nip calender, we prefer to cure the fabric in an oven at a temperature ranging from about 250 F. to about 400 F., for a period of time ranging from about 15 minutes to about 2 minutes.
We prefer to give the fabric a final washing treatment to remove soluble materials and any superficial mechanical finish present on the fabric and also, as previously stated, to remove the mechanical finish which has-been applied to: the unprinted part ofthe fabric. This washing is preferably done in the open width. by a light soaping treatment in a dilute soapv solution followed by thorough washing in hot water. The fabric is finally squeezed and dried.
Thatthe pattern does not mark off even when using a hot friction calender, we attribute to. the fact that the d'yestuifis. present inthe printing paste primarily in a molecular or semi-molecular form rather than in large pigment particle form, so that when printed and partly dried, the. dyestuif penetrates and adheres to the fabric. and stays there during the calendering rather than sticking on the hot bowl and then marking off on the cloth. Thus, if the same dyestufi as sold in pigment form is added to the same printing paste, printed; dried, and calendered, it will. be found to smear and mark-on" within a few yards.
It is impossible. to develop the vat dyestufi after printing and before calenderingsince such treatment would smear the pattern. The usual steam aging method of developing vat prints cannot be used prior to calendering since the steam aging sets up the resinous material, resulting in a non-durable mechanical finish. To develop the dyestufi after calendering and curing is also impractical since the strong chemical treatments at elevated temperatures necessary to develop the dyes will either destroy or seriously reduce the mechanical finish.
If desired, the cured fabric may be run through an oxidizing solution to insure complete conversion of the leuco dyestuff to. the. keto. or insoluble. form. For this. purpose, for example, hydrogen peroxide, sodium perborate, and potassium dichromate may be used. This step, however, is not necessary since ithas. been found that the contact with the air during printing, drying, and curing, has for all practical purposes already converted the dyestuif to the keto or insoluble form.
Instead of using caustic soda. and sodium. hydrosulphite to reduce and disperse the vat. dyestufi, other methods well known in the art may be used. For example, the caustic soda may be substituted by potassium hydroxide, trisodium phosphate, soda ash, triethanolamine, and other strong alkalies. The hydrosulphite maybe substituted by sodium sulfoxylate formaldehyde, sodium ibisulphi-te, sodium hydrosulphite formaldehyde, and others. For all practical purposes, sodium liydrosulphite and caustic soda are used in proportions which vary according to dyestulf but which are well known in the art.
The percentage of thermo-setting material in the printing may be varied between wide limits, depending upon the degree of stillnessv desired in the printed. portion. The latter may vary between a softflexible print. approaching the unprinted part of the cloth. in hand to a firm stifi pattern imposed upon a soft flexible background of unprinted cloth. In general, we. operate. between 6% thermosetting materialin the printin gum to 25% by weight of the paste.
The percentage of dyestuir'may also be varied. It is, of course, rather difiicult: to give a: lower limit since. the printing; paste may be applied: in the tinted form, in. which case. only a very small quantity of dyestuif is used, say .l% by weight of the paste. The upper limit on the percentage of dyestuif varies, depending upon the ease with which a dyestuif will. mark. ofi during the mechanical processing and. also upon many other factors, such as percentage of moisture in the printybefore the; mechanical: treatmenitis; applied. type of gum, lubricant, and other ingredients. of theprinting paste, quantity of paste deposited by the printing" machine, and heat, pressure and friction applied during the mechanical processing Commercial operations have indicated that in general we may operate-with. a dyestuff percentage; of..1,2% by weight in the printing; using a hot friction glazer which: is the most. difficult machine. to operate as far as mark-off and smearing are concerned.
Where the patterns. represent approximately 80% coverage, no difficulty is encountered in passing the fabric through the friction calender. In. the friction calender, however, if the coverage is substantially less, than 80%, then it is desirable, in order to prevent chewing of the fabric, to size the fabric before printing with a sizing producing. substantially the. same coefiicient of friction as the printed areas after printing. The sizing solution should contain a small percentage of the lubricants mentioned previously, usually about 10% by weight, and may in addition also contain a small percentage of some stiffening agent such as, for example, dextrin, casein, glucose, and starch.
The fabric after curing or after washing and drying, may be subjected to further auxiliary textile treatments to produce new and novel effects. For example, a sheer lawn having the lustrous colored patterns applied may be subjected to cellulose swelling treatments such such as, for example, treatments with cuprammonium solutions and caustic sodium zincate solutions to produce organdy effects, the final results. being alustrous colored pattern on a sheer organdy fabric.
In a similar manner, it is possible to overdye the finished cloth and obtain the lustrous colored patterns on a dyed background.
In all such. after treatments, it is essential that they be so chosen that. they do not detrimentally affect the lustrous colored pattern already applied. This danger may be somewhat reduced by using as a lubricant materials which have durable water repellent properties such as, for example, stearamidomethylpyridinium chloride and stearyloxymethylpyridinium chloride.
Example I The printing paste was made by first preparing the molecular or the very fine dispersion of the vat" dye-stuff. The following formula was used to prepare this dispersion:
Parts by weight Ponsol Jade Green Dbl/Paste (C. I. 1101) 766 Caustic soda, 75 deg. T. W.- 460 Sodium hydrosulphite 259 Blancol (sodium naphthalene disulphonateformaldehyde) 307 Acetic acid, 510 Water 7698 The Blancol was dissolved in one-half of the total amount. of. water and the. color then added. The whole mixture was mixed very thoroughly. To this was then added first the caustic soda and then sodium hydrosulphite with agitation. and' Aerotex M-3 (methyl-methylol melamine) 2080 Ammonium thiocyanate 208 Carbowax 1500 (polymerized ethylene oxide) 416 Water 3136 The vat dyed dispersion previously prepared was first added to the Supertex Gum T-125 and then carefully mixed. The Aerotex M43 resin was dissolved in water and added with thorough agitation. The Carbowax 1500 and the ammonium thiocyanate were put in solution and added with careful mixing. After that, the paste was strained and a smooth, uniform paste of good printing property was obtained.
A 40", 48/48, 3.50, cotton fabric which had previously been purified through the regular bleaching process was printed by passing it through a regular textile printing machine followed by careful drying, so that approximately 10% moisture above the normal moisture remained in the printed portion of the cloth. The cloth was then taken to a conventional friction calender having a friction ratio of 3:1, a total pressure of 40 tons, and a temperature of the upper steel bowl of approximately 350 F. The cloth was given three runs through this calender and during this procedure, no mark-off, smearing, or staining of the unprinted portion of the cloth took place.
tests and light tests conducted on this fabric showed excellent durability both as far as color and finish were concerned.
Example If A dispersion of reduced vat dyestuff was prepared as described in Example I, except that Ponsol Violet BN Paste (C. I. 1163) was used as the dyestuff.
The printing paste used in'this case had the following composition:
Parts by weight Reduced dispersion of Violet BN Paste as prepared above 2000 Supertex T-125 2000 Aerotex Cream 450 (urea-formaldehyde resin, 50%) 833 Rhonite 414 (urea-formaldehyde resin,
40%) 1667 Ammonium thiocyanate 200 Sapamine KW (tri-methyl ammonium methyl sulfate of monostearylmethaphenylene diamine) 400 Water 2900 This paste was prepared by adding the reduced dispersion of the vat acid to the Supertex Gum with good mechanical stirring. The Aerotex 450, Rhonite 414, Sapamine KW, and the ammonium thiocyanate were dissolved in water and added with thorough mixing to the Supertex Gum containing the reduced acid. The paste was then strained in the usual manner, producing smooth, homogeneous paste of good printing properties.
A 40", 46/40, 3.50, spun rayon fabric was presized by padding it through a solution containing dextrine and /2% sulphonated tallow by weight and then framing to width.
The cloth so prepared was printed in the regular printing machine, using the conventional methods of printing and using the printing pastes described above. The cloth after printing was carefully dried until approximately 10% of residual moisture above the normal moisture remained in the printed portions of the fabric. This fabric was then passed once through a 5-bowl heavyweight chasing calender, using a temperature of 300 F. on the heated bowls and a total pressure of 30 tons on the machine.
After chasing the fabric was cured in a loop type aging chamber for 5 minutes at 310 F.
The cloth was then washed through a warm solution containing a small quantity of detergent and alkaline material, followed by a thorough washing in warm water.
The fabric was then extracted and frame dried.
The resulting cloth had a mellow, deep-seated lustrous, colored pattern imposed upon a dull white background of unprinted cloth. This eifect was durable to drycleaning, soaping, treatments, and light.
Example III Dispersion of the leuco base was prepared as previously described, using the following formulation:
Parts by weight Indanthrene Red Violet RHA Paste Fine (0. I. 1212) 766 Potassium hydroxidesolid 109 Sodium hydrosulphite 259 Blancol 307 Formic acid, 88% 157 Water 8402 Reduction is carried out in the same manner as described for Example I.
A printing paste having the following composition was prepared:
Parts by weight Indanthrene Red Violet RHA Paste Fine reduced vat solution as prepared above 2080 Locust bean gum-5% 2780 Aerotex M-3 750 Diammonium phosphate 624 Aerotex Softener H 416 Water 3350 The vat acid is added to the locust bean gum and thoroughly mixed. The Aerotex M-3, diammonium phosphate, and Aerotex Softener H are dissolved and added under constant agitation, after which'the paste is strained.
' Printing and processing are handled the same as for ExampleI.
Example IV A four-color lustrous printed pattern on a dull dyed fabric was obtained.
Example V A printing paste of the following composition was made up:
Parts by weight Algosol Green lBW Paste (C. I. 1101) 75 Carbowax 1500 1000 Lactic acid (85%) 100 Ammonium thiocyanate 120 Aerotex M-3 2000 Sodium nitrite 150 Supertex T-125 4000 Water 2400 Color was pasted with small amount of water, added to Supertex T125, and mixed thoroughly. Sodium nitrite, Aerotex M-3, and Carbowax 1500, put into solution and added in order. Finally, the lactic acid (85%) and ammonium thiocyanate in water solution were added and the total mixture was strained. Printing and processing was carried out as described in Example I.
We claim:
1. The process of producing durable colored lustrous pat-tern efiects on cellulose textile fabrics which consists in printing the fabric with the desired pattern with an aqueous printing paste containing a vat dyestuff in free leuco base form and thermosetting acid-curing resin forming materials, said paste containing a sufficient quantity of acidic material to ensure the existence of an acid environment during the heating hereinafter mentioned, drying the printed fabric to from 5% to moisture by weight of the fabric above natural moisture content, passing the dried fabric through a pressure mechanical finishing machine, heating to polymerize the resin forming materials to insoluble form, and washing the fabric.
2. The process of claim 1 in which the dyestuff is an anthraquinone.
3. An aqueous printing paste for use in producing durable mechanical colored lustrous pattern effects on cellulose textile fabrics, which tern efiects on cellulose textile fabrics, which consists essentially of Water, printing gum, vat dyestuff in free leuco base form, thermosetting acid-curing resin-forming materials, an acidic catalyst, and a softener.
6. The process of claim 1 in which the dyestuif is a thio-indigo.
7. A printing paste according .to claim 3 in which the dyestuff is a thio-indigo.
8. The printing paste of claim 5 in which a textile lubricant is employed in lieu of a softener.
9. A printing paste according to claim 5 in which a textile lubricant is employed in addition to a textile softener.
GEORGE ALAN BILLINGSLEY, JR. WILLIAM P. HALL.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,909,221 Paquin May 16, 1933 2,123,153 Rivat July 5, 1938 2,169,546 Widmer Aug. 15, 1939 2,267,609 Kern Dec. 23, 1941 OTHER REFERENCES Textile Manufacturer for March 1949, page 132.
Textile Manufacturer for December 1946, page 647.
Application and Properties of Vat Dyes, Calco Tech. Bull. #802, June 1948, American Cyanamid Co., Bound Brook, N. J page 19.
Claims (1)
1. THE PROCESS OF PRODUCING DURABLE COLORED LUSTROUS PATTERN EFFECTS ON CELLULOSE TEXTILE FABRICS WHICH CONSISTS IN PRINTING THE FABRIC WITH THE DESIRED PATTERN WITH AN AQUEOUS PRINTING PASTE CONTAINING A VAT DYESTUFF IN FREE LEUCO BASE FORM AND THERMOSETTING ACID-CURING RESIN FORMING MATERIALS, SAID PASTE CONTAINING A SUFFICIENT QUANTITY OF ACIDIC MATERIAL TO ENSURE THE EXISTENCE OF AN ACID ENVIRONMENT DURING THE HEATING HEREINAFTER MENTIONED, DRYING THE PRINTED FABRIC TO FROM 5% TO 15% MOISTURE BY WEIGHT OF THE FABRIC ABOVE NATURAL MOISTURE CONTENT, PASSING THE DRIED FABRIC THROUGH A PRESSURE MECHANICAL FINISHING MACHINE, HEATING TO POLYMERIZE THE RESIN FORMING MATERIALS TO INSOLUBLE FORM, AND WASHING THE FABRIC.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20114A US2592852A (en) | 1948-04-09 | 1948-04-09 | Process of producing dyed lustrous printed pattern effects using acidcuring resins and free leuco bases of vat dyes |
| DEP29463D DE845337C (en) | 1948-04-09 | 1949-01-01 | Aqueous printing paste for the production of colored, glossy pattern effects on fabrics made from vegetable fibers and processes for creating pattern effects |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20114A US2592852A (en) | 1948-04-09 | 1948-04-09 | Process of producing dyed lustrous printed pattern effects using acidcuring resins and free leuco bases of vat dyes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2592852A true US2592852A (en) | 1952-04-15 |
Family
ID=21796836
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US20114A Expired - Lifetime US2592852A (en) | 1948-04-09 | 1948-04-09 | Process of producing dyed lustrous printed pattern effects using acidcuring resins and free leuco bases of vat dyes |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2592852A (en) |
| DE (1) | DE845337C (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2722489A (en) * | 1952-08-16 | 1955-11-01 | Gen Aniline & Film Corp | Process of coloring glass fabrics with vat dyes |
| US2882280A (en) * | 1955-02-14 | 1959-04-14 | Pittsburgh Coke & Chemical Co | Dibenzanthrone vat dyestuffs |
| FR2014360A1 (en) * | 1968-06-28 | 1970-04-17 | Sandoz Sa |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE937583C (en) * | 1952-06-04 | 1956-01-12 | Cassella Farbwerke Mainkur Ag | Kuepen dye preparations suitable for textile printing |
| DE1045365B (en) * | 1956-11-13 | 1958-12-04 | Basf Ag | Viscous dye or pigment-containing printing pastes of the oil-in-water type |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1909221A (en) * | 1930-10-20 | 1933-05-16 | Gen Aniline Works Inc | Printing colors and process of preparing them |
| US2123153A (en) * | 1935-04-04 | 1938-07-05 | Celanese Corp | Printing and other textile treatments |
| US2169546A (en) * | 1936-09-17 | 1939-08-15 | Soc Of Chemical Ind | Fixing dyestuffs on substrata |
| US2267609A (en) * | 1939-01-28 | 1941-12-23 | Nat Aniline & Chem Co Inc | Vat dye composition |
-
1948
- 1948-04-09 US US20114A patent/US2592852A/en not_active Expired - Lifetime
-
1949
- 1949-01-01 DE DEP29463D patent/DE845337C/en not_active Expired
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1909221A (en) * | 1930-10-20 | 1933-05-16 | Gen Aniline Works Inc | Printing colors and process of preparing them |
| US2123153A (en) * | 1935-04-04 | 1938-07-05 | Celanese Corp | Printing and other textile treatments |
| US2169546A (en) * | 1936-09-17 | 1939-08-15 | Soc Of Chemical Ind | Fixing dyestuffs on substrata |
| US2267609A (en) * | 1939-01-28 | 1941-12-23 | Nat Aniline & Chem Co Inc | Vat dye composition |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2722489A (en) * | 1952-08-16 | 1955-11-01 | Gen Aniline & Film Corp | Process of coloring glass fabrics with vat dyes |
| US2882280A (en) * | 1955-02-14 | 1959-04-14 | Pittsburgh Coke & Chemical Co | Dibenzanthrone vat dyestuffs |
| FR2014360A1 (en) * | 1968-06-28 | 1970-04-17 | Sandoz Sa |
Also Published As
| Publication number | Publication date |
|---|---|
| DE845337C (en) | 1952-07-31 |
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