US2256809A - Production of resist effects - Google Patents
Production of resist effects Download PDFInfo
- Publication number
- US2256809A US2256809A US242745A US24274538A US2256809A US 2256809 A US2256809 A US 2256809A US 242745 A US242745 A US 242745A US 24274538 A US24274538 A US 24274538A US 2256809 A US2256809 A US 2256809A
- Authority
- US
- United States
- Prior art keywords
- resist
- oxidation
- parts
- radical
- amino
- 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
- 230000000694 effects Effects 0.000 title description 30
- 238000004519 manufacturing process Methods 0.000 title description 25
- -1 amino cresol Chemical compound 0.000 description 57
- 230000003647 oxidation Effects 0.000 description 51
- 238000007254 oxidation reaction Methods 0.000 description 50
- 239000000463 material Substances 0.000 description 43
- 238000010019 resist printing Methods 0.000 description 41
- 239000003086 colorant Substances 0.000 description 38
- 229920000768 polyamine Polymers 0.000 description 27
- 239000000984 vat dye Substances 0.000 description 25
- 125000001931 aliphatic group Chemical group 0.000 description 23
- 238000000034 method Methods 0.000 description 21
- 150000003254 radicals Chemical class 0.000 description 20
- 239000004753 textile Substances 0.000 description 18
- 238000007639 printing Methods 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 13
- 239000002562 thickening agent Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 11
- 230000008569 process Effects 0.000 description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 239000000975 dye Substances 0.000 description 8
- 239000004744 fabric Substances 0.000 description 8
- 230000018109 developmental process Effects 0.000 description 7
- 239000000835 fiber Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 230000032683 aging Effects 0.000 description 5
- 239000003513 alkali Substances 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 238000010025 steaming Methods 0.000 description 4
- FWLHAQYOFMQTHQ-UHFFFAOYSA-N 2-N-[8-[[8-(4-aminoanilino)-10-phenylphenazin-10-ium-2-yl]amino]-10-phenylphenazin-10-ium-2-yl]-8-N,10-diphenylphenazin-10-ium-2,8-diamine hydroxy-oxido-dioxochromium Chemical compound O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.O[Cr]([O-])(=O)=O.Nc1ccc(Nc2ccc3nc4ccc(Nc5ccc6nc7ccc(Nc8ccc9nc%10ccc(Nc%11ccccc%11)cc%10[n+](-c%10ccccc%10)c9c8)cc7[n+](-c7ccccc7)c6c5)cc4[n+](-c4ccccc4)c3c2)cc1 FWLHAQYOFMQTHQ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical class NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 3
- 239000004615 ingredient Substances 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
- 239000007800 oxidant agent Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 229920000767 polyaniline Polymers 0.000 description 3
- UAJUXJSXCLUTNU-UHFFFAOYSA-N pranlukast Chemical compound C=1C=C(OCCCCC=2C=CC=CC=2)C=CC=1C(=O)NC(C=1)=CC=C(C(C=2)=O)C=1OC=2C=1N=NNN=1 UAJUXJSXCLUTNU-UHFFFAOYSA-N 0.000 description 3
- 229960004583 pranlukast Drugs 0.000 description 3
- 239000000264 sodium ferrocyanide Substances 0.000 description 3
- GTSHREYGKSITGK-UHFFFAOYSA-N sodium ferrocyanide Chemical compound [Na+].[Na+].[Na+].[Na+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] GTSHREYGKSITGK-UHFFFAOYSA-N 0.000 description 3
- 235000012247 sodium ferrocyanide Nutrition 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- ZLHGTHCCYUEAIK-UHFFFAOYSA-N 5,7-dibromo-2-(5,7-dibromo-3-hydroxy-1H-indol-2-yl)indol-3-one Chemical compound [O-]c1c([nH]c2c(Br)cc(Br)cc12)C1=[NH+]c2c(cc(Br)cc2Br)C1=O ZLHGTHCCYUEAIK-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- UGCDBQWJXSAYIL-UHFFFAOYSA-N vat blue 6 Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2Cl)=C1C1=C2NC2=C(C(=O)C=3C(=CC=CC=3)C3=O)C3=CC(Cl)=C2N1 UGCDBQWJXSAYIL-UHFFFAOYSA-N 0.000 description 2
- RNJIWICOCATEFH-WCWDXBQESA-N (2e)-2-(1-oxobenzo[e][1]benzothiol-2-ylidene)benzo[e][1]benzothiol-1-one Chemical compound C1=CC=CC2=C(C(C(=C3/C(C4=C5C=CC=CC5=CC=C4S3)=O)/S3)=O)C3=CC=C21 RNJIWICOCATEFH-WCWDXBQESA-N 0.000 description 1
- VMXWZRNWXZSSCE-VXPUYCOJSA-N (2z)-6-ethoxy-2-(6-ethoxy-3-oxo-1-benzothiophen-2-ylidene)-1-benzothiophen-3-one Chemical compound S/1C2=CC(OCC)=CC=C2C(=O)C\1=C1/C(=O)C2=CC=C(OCC)C=C2S1 VMXWZRNWXZSSCE-VXPUYCOJSA-N 0.000 description 1
- YHYKLKNNBYLTQY-UHFFFAOYSA-N 1,1-diphenylhydrazine Chemical compound C=1C=CC=CC=1N(N)C1=CC=CC=C1 YHYKLKNNBYLTQY-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 description 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- MRQIXHXHHPWVIL-ISLYRVAYSA-N Sudan I Chemical compound OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=CC=C1 MRQIXHXHHPWVIL-ISLYRVAYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- MMCPOSDMTGQNKG-UHFFFAOYSA-N anilinium chloride Chemical compound Cl.NC1=CC=CC=C1 MMCPOSDMTGQNKG-UHFFFAOYSA-N 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- YOCIQNIEQYCORH-UHFFFAOYSA-M chembl2028361 Chemical compound [Na+].OC1=CC=C2C=C(S([O-])(=O)=O)C=CC2=C1N=NC1=CC=CC=C1 YOCIQNIEQYCORH-UHFFFAOYSA-M 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 229930003836 cresol Natural products 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 229940097275 indigo Drugs 0.000 description 1
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 235000012738 indigotine Nutrition 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- XKLJHFLUAHKGGU-UHFFFAOYSA-N nitrous amide Chemical compound ON=N XKLJHFLUAHKGGU-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- LLBIOIRWAYBCKK-UHFFFAOYSA-N pyranthrene-8,16-dione Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3C=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1C=C4C=C5 LLBIOIRWAYBCKK-UHFFFAOYSA-N 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical group [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 1
- KIEOKOFEPABQKJ-UHFFFAOYSA-N sodium dichromate Chemical compound [Na+].[Na+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O KIEOKOFEPABQKJ-UHFFFAOYSA-N 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 239000000988 sulfur dye Substances 0.000 description 1
- JXUKQCUPTNLTCS-UHFFFAOYSA-N vat green 1 Chemical compound C1=CC=C[C]2C(=O)C(C3=C45)=CC=C4C(C4=C67)=CC=C7C(=O)[C]7C=CC=CC7=C6C=C(OC)C4=C5C(OC)=CC3=C21 JXUKQCUPTNLTCS-UHFFFAOYSA-N 0.000 description 1
- KOTVVDDZWMCZBT-UHFFFAOYSA-N vat violet 1 Chemical compound C1=CC=C[C]2C(=O)C(C=CC3=C4C=C(C=5C=6C(C([C]7C=CC=CC7=5)=O)=CC=C5C4=6)Cl)=C4C3=C5C=C(Cl)C4=C21 KOTVVDDZWMCZBT-UHFFFAOYSA-N 0.000 description 1
- KJPJZBYFYBYKPK-UHFFFAOYSA-N vat yellow 1 Chemical compound C12=CC=CC=C2C(=O)C2=CC=C3N=C4C5=CC=CC=C5C(=O)C5=C4C4=C3C2=C1N=C4C=C5 KJPJZBYFYBYKPK-UHFFFAOYSA-N 0.000 description 1
- YKSGNOMLAIJTLT-UHFFFAOYSA-N violanthrone Chemical compound C12=C3C4=CC=C2C2=CC=CC=C2C(=O)C1=CC=C3C1=CC=C2C(=O)C3=CC=CC=C3C3=CC=C4C1=C32 YKSGNOMLAIJTLT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/12—Reserving parts of the material before dyeing or printing ; Locally decreasing dye affinity by chemical means
Definitions
- the present invention relates to the production of white and colored resist or reserve styles on ground shades obtained with oxidation colors,
- the oxidation colors comprise an important class oi dyestuffs which may be employed for the dyeing and printing of textile materials, such as natural and artificial cellulosic fibers, and natural silk. These colors upon oxidation in the presence of the fiber are converted to complex insoluble coloring matters. 'They include aromatic amino compounds, such as aniline and aminodiphenylamine, which are oxidizable to form black dyeings, and para phenylene diamine, meta amino cresol, diam'sidine, etc.', which are oxidizable to form fast brown colorations on textile materials.
- the oxidation colors also include the soluble leuco ester salts of vat dyes which upon oxidation in the presence of the fiber are productive of dyeings of various shades.
- oxidation colors denotes and includes colors which are applied directly to the material and then'developed by oxidation under acid conditions.
- a conventional method of applying oxidation colors to a textile material involves padding the textile material with a solution of the. desired oxidation color, drying the thus padded material, and then developing the color by a procedure including aging and steaming,
- alkylol-monoamines have been used, but they are not entirely satisfactory because they are relatively weakly alkaline and to obtain suflicient alkalinity they must be used in large proportions. Further, these compounds are liquids which have a tendency to spread, and the prints obtained with pastes containing them tend to be sticky and to mark-off.
- resist pastes tion of the pastes applied .to selected areas of the materials is to resist the development of the ground colors, for simplicity in terminology, effects .of this type are referred to herein as duction of the eflects are termed resist pastes.
- a further object of the-invention is to provide a process for the production of colored resist styles on oxidation colors, the said styles being obtained with the use of resist printing pastes containing vat dyes.
- a further object of the invention is to provide novel white and colored resistprinting pastes which are adapted for use in the production of resist styles with oxidation colors.
- resist printing pastes are produced which, when employed in place of the conventional resist printing pastes in the productionof white and colored resist efiects on ground colorations obtained with oxidation colors, are productive of efiects which are clearly outlined and are substantially free from undesirable fiushing.
- the hydroxylated aliphatic polyamines employed in the resist printing pastes of the invention are aliphatic polyamines in which the amino groups may be unsubstituted, but at least one amino group preferably contains as a substituent at least one alkyl or aralkyl radical.
- the central radical of these compounds is an aliphatic radical which may consist of a single alkyl radical or a plurality of alkyl radicals linked together by a non-carbon atom or group, such as, for example, 0, f5, and NXs, wherein X5 represents hydrogen, alkyl, aralkyl, or hydroxyalkyl.
- non-carbon linkages denotes O, S and NX5 as herein defined.
- the compounds contain at least one hydroxyl group which may be in the central aliphatic radical, or in an N-alkyl radical, or both.
- the hydroxylated aliphatic polyamines may be represented by the following general formula:
- R represents an alkyl radical or a radical consisting of a plurality of alkyl radicals linked together by non-carbon atoms or groups such as O, S, and NXs, (wherein. X5 has the above meaning); X1, X2, IQ, and X4 each represents hydrogen, an alkyl radical, an aralkyl radical, a hydroxyalkyl radical, or two of the X's of X1, X2, X1, X4 joined to different nitrogen atoms conjointly represent a bivalent alkyl radical; and n .represents a small whole number.
- X1, X2, X3, and X4 represents a 'hydroxyalkyl radical. It is preferred to employ compounds in which the amino groups are substituted by at least one and prefererably by two or more hydroxyalkyl radicals, regardless of whether the radical represented by R contains hydroxyl groups.
- radical represented by B may contain hydroxyl groups as substituents.
- radical contains 1 to 3 ethylene groups which, in cases where this radical contains more than one ethylene group, are linked together by O, S, or NXs, X5 having the above meaning. Further, the preferred compounds contain at least one, and preferably two or more, hydroxyethyl radicals as substituents in the amino groups.
- the lower carbon chain compounds of ,the above type have low melting points, and are viscous liquids at ordinary temperatures; the viscosity of the compounds increasing with increase in their molecular weight.
- the high molecular chain compounds on the otherhand, are crystalline or amorphous solids which melt above 50 C. All of the compounds of the above type are of low volatility and possess high solubility in water, alcohol, and in most organic solvents.
- the hydroxylated aliphatic polyamines of the above type are further characterized by an exceedingly strong alkaline character.
- the superior prints obtainable by the process of the present invention are probably due in great measure'to the fact that because of the exceedingly high basic character of the hydroxylated aliphatic polyamines the amount of alkaline reacting substances used in the preparation of resist printing
- this radical may contain other substituents which do not alter the essential characteristics of the compounds, such as, for example, alkoxy or aralkyloxy radicals.
- the alkyl and aralkyl radicals attached to the amino groups of the compounds may contain substituents, especially hydroxyl groups. In this connection itshould be noted that where an N-aralkyl,
- radical contains two or more carbon atoms in the alkyl radical thereof and this alkyl radical contains hydroxyl groups as substituents, it is regarded as a hydroxyalkyl radical for the purposes of this invention.
- those which are generally preferred for use in the re--, sist pastes of the invention are hydroxylated aliphatic diamines in which the central aliphatic pastes may be lowered to a relatively small quantity which by virtue of its paucity avoids the flushing and spreading of the printed surface while at the same time it efiiciently inhibits the development of the oxidation color employed as the ground shade.
- the hydroxylated aliphatic polyamines exert solubilizing action on the leuco vat dyes which assists in causing them to penetrate. the fiber, thereby producing superior prints.
- the compounds of the above class which are solids are valuable because printed areas containing them, on being dried out, are free from stickiness.
- any one or a mixture of a wide variety of hydroxylated aliphatic polyamines which contain at least one N-alkyl group containing at least two carbon atoms and at least one hydroxyl group may be employed in the preparation of the resist printing pastes of the present'invention.
- polyamines may be mentioned the following compounds:
- the resist printing pastes of the present invention may be prepared in a simple manner.
- toprepare resist printing pastes for the production of white resist effects on oxidation colors there may be added to the usual thicken- 75 in the usual manner with the following solution ing ingredients of such pastes one or a mixture of the hydroxylated aliphatic polyamines of the above type.
- White resist eifects on oxidation colors may be obtained .in accordance with the present invention by applying this resist printing paste in the conventional manner to a fabric which has been prepared with a. composition containing the oxidation color desired for the ground shade. Thereafter, the-textile material is subjected to a conventional developing treatment whereupon a white resist effect is obtained on the developed ground;
- This development treatment may include merely a steaming and aging procedure where that is sufliclent to oxidize the ground color (which has been applied tothe materialin a solution containing an oxidizing agent). It may include, however, an acid aging or, after the usual steaming and aging, a passage of the material through an oxidizing bath containing an oxidizing agent and an acid.
- Example 1 White cotton material is prepared for aniline black:
- the cloth is padded therewith, then dried and printed with the following white resist printing paste:
- the material After printing,- the material is steamed for about 2 minutes at 102 0., in arapid ager, then passed into an oxidation bath composed of /2 per cent sodium bichromate and 1 per centof a 28 0 per cent solution of' acetic acid. The printed material is then rinsed, soaped, rinsed, and dried. A white resist print is thus obtained on the aniline black ground.
- Example 2.-A white resist printing effect on a fast brown ground may be obtained as follows:
- a white cotton and rayon mixed fabric is prepared with a padding liquor which is made by mixing the following three solutions:
- the fabric is dried, preferably in hot air and then printed with the resist paste described in Example 1.
- the ma terial is passed through a rapid ager for about 5 to 10 miflutes at 105 C.
- the fabric may then be subjected to ammonia vapors or may be rinsed immediately after steaming in luke warm water, soaped, rinsed and dried.
- Example 3 A natural silk fabric is padded with the following padding liquor:
- the whole is standardized to 1000 parts total.
- the silk material is then printed with a white resist paste composed of: e
- the material is steamed for about 5 minutes whereby the brown ground shade'is developed and the fabric is passed into tepid water, rinsed thoroughly, soaped, rinsed and dried. Thus, a white resist effect is obtained on a brown bottom shade.
- Colored resist efiects on oxidation colors may be obtained in accordance with the present invention with the use of printing pastes containing dyes of various types, it being only necessary that such dyes be applicable to a textile material in an alkaline paste.
- colored resist effects may be obtained with the use of resist printing pastes containing dyes, such as vat dyes, sulfur dyes, and azoic printing compositions (e. g., nitrosamine and diazo-amino compositions).
- the present invention is particularly directed to the production of. resist printing pastes containing vat dyes and the above-described hydroxylated aliphatic polyamines.
- Vat dye resist printing pastes may be prepared in accordance with the present invention by incorporating with the usual components of a vat dye printing paste (which ordinarily include a vat dye in the unreduced form, thickening ingredients, a reducing agent, such as sodium formaldehyde sulfoxylate, an alkali carbonate or caustic alkali, and dispersing agents, and other suitable additions) a hydroxylated aliphatic polyamine of the type already described.
- a vat dye printing paste which ordinarily include a vat dye in the unreduced form, thickening ingredients, a reducing agent, such as sodium formaldehyde sulfoxylate, an alkali carbonate or caustic alkali, and dispersing agents, and other suitable additions
- a hydroxylated aliphatic polyamine of the type already described.
- the total amount of alkaline material ordinarily employed in such printing pastes may be reduced in most cases to a minimum because of the strongly basic character
- Colored resist efiects may be obtained on oxidation color ground dyeings in accordance with the present invention by locally applying ⁇ a vat dye resist printing paste of the above type to a textile material which has been previously prepared with a grounding liquor containing an oxidation color, and then subjecting the material to a development treatment.
- a vat dye resist printing paste of the above type to a textile material which has been previously prepared with a grounding liquor containing an oxidation color, and then subjecting the material to a development treatment.
- the following examples are illustrative'of procedures carried out in accordance. with the present invention wherein colored resist effects are obtained with vat dyes on ground shades of oxidation colors.
- the parts are by weight:
- Example st-Cotton material is prepared with the aniline black padding solution described in Example 1, and is then printed with the following vat dye composition:
- Example 5 Cotton material is padded with the following solution and then dried.
- the material After printing and drying, the material is passed through a vat dye ager for about 4 to 5 minutes, whereby the printed Vat Orange R is developed; thereafter, the material may be passed for about 3 to5'minutes into an acid ager which will cause the ground shade to be developed, but not in the areas where the resist has been applied by the printing. Instead-of devel. oping the ground shade in an acid ager, it may be developed by padding the material with a solution containing per '1000 parts:
- a very fast and brilliant orange print is thus obtained on a dyed vat blue ground shade.
- the general procedure described in the above example may be used for the preparation of white resists on ground colorations obtained with leuco ester salts of vat dyes by using in place of the vat dye resist printing paste the white resist printing pastes described in Examples 1 and 3.
- the development is similar to that described in Example 5, being carried out by subjecting the material to an acid aging treatment or padding it with the acid padding liquor illustrated above.
- vat dye selected from the following group:
- the proportions of ingredients specified for preparation of the resist printing pastes in the foregoing examples may be varied within wide limits.
- the total amount of alkaline materials in the pastes may be reduced to a minimum.
- one or more of the hydroxylated ali-' phatic polyamines may be used in place of the entire amount of alkali normally used in pastes for the production of resist effects of this type. In other instances, superior results are obtained by replacing only a part of the alkali normally used with one or more of the amines.
- the amines in place of at least a part of the alkali normally used; i.'e., they are used as alkaline agents.
- the'particular proportions to be employed in any given case are dependent upon the character of the textile material employed, the type of effect desired, and the kind of development treatment. Hence, these proportions may be left largely to the'dlscretion of the operator.
- the foregoing examples, however, are illustrative oftypical procedures and may be referred to as a basis for comparison.
- the resist effects by applying the resist pastes to a material impregnated with a ground color is not limited to this manner of proceeding since the resist pastes may be applied to the material before impregnation with the ground color.
- a resist printing paste for the production of resist eflects on oxidation colors comprising a thickener and a hydroxylated aliphatic polyamine free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals.
- a resist printing paste for the production of colored resist effects on oxidation colors comprising a dye applicable to textile materials in an alkaline paste, a thickener, and a hydroxylated aliphatic polyamine free from amino substituents other than alkyl radicals, aralkyl radicals, and hydroxyalkyl radicals.
- a resist printing paste for the production of resist effects on oxidation colors comprising a thickener and a hydroxylated aliphatic polyamine having as a central radical a plurality of alkyl radicals linked together by non-carbon linkages, said polyamine being free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals and containing at least one hydroxyalkyl radical as an amino-substituent when the'central radical is free from hydroxyl groups.
- a resist printing paste for the production of colored resist effects on oxidation colors comprising a dye applicable to textile-materials in an alkaline paste, a thickener, and a hydroxylated aliphatic polyamine having as a central radical as illustrative a plurality ofallwl radicals linked together, by
- phatic polyamines of the class disclosed above cals, aralkyl radicals and-hydroxyalkyl radicals
- thickener and a hydroxylated aliphatic poly-
- amine having as a central radical a plurality of alkyl radicals linked together by non-carbon linkages, said polyamine being free from amino-ubstituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals and containing at least one hydroxy-allwl radical as an amino-substituent when the central radical is free from hydroxyl groups.
- a resist printing paste for the production of resist effects on oxidation colors comprising a thickener and a hydroxyalkylated ethylenediamine which contains at least one hydroxyalkyl radical as an amino-substituent and which is free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals.
- a resist printing paste for the production of colored resist efiects on oxidation colors comprising an unreduced vat dye, a thickener, and a hydroxyalkylated ethylenediamine which contains at least one hydroxyalkyl radical as an amino-substituent and which is free from aminosubstituents other than alkyl radicaIs araIkyI radicals and hydroxyalkyl radicals.
- the improvement which comprises applying to selected areas of a textile material impregnated with an undeveloped oxidation color a resist printing paste comprising a dye applicable to textile materials in an alkaline paste, a thickener, and a hydroxylated aliphatic polyamine free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals.
- a reducing agent a thickener, and a hydroxylated aliphatic polyamine having as a central radical a plurality of alkyl radicals linked together by non-carbon linkages, said polyamine being free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals and containing at least one hydroxyalkyl radical as an amino-substituent when the central radical is free from hydroxyl groups.
- a resist printing paste comprising a thickener and a hydroxyalkylated ethylenediamine which contains at least one hydroxyalkyl free from amino-substituents other than alkyl radicals, araikyl radicals and hydroxyalkyl radi- 11.
- a resist printing paste for the production of resist effects on oxidation colors comprising a thickener and 1,2-bis- (di-Zf-ethanol-amino) ethane.
- a resist printing paste for the production of resist eflects on oxidation colors comprising a thickener and bis-(di-2',3'-propan-diol-2-aminoethyl) ether.
- a resist printing paste for the production of resist eflects on oxidation colors comprising a thickener and bis -(di 2'- ethanol 2 aminoethyl-) sulfide.
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- Engineering & Computer Science (AREA)
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Description
Patented Sept. 23, 1941 UNITED STATES PATENT OFFICE.
PBODUCTION F RESIST EFFECTS Jean G Kern, East Aurora, N; Y., assignor to National Aniline & Chemical Company, Inc., New. York, N. Y., a corporation of New York No Drawing.
Application November 28, 1938,
Serial No. 242,745
13 Claims.
The present invention relates to the production of white and colored resist or reserve styles on ground shades obtained with oxidation colors,
and, in particular, it relates to the production of colored resist styles on ground shades obtained with oxidation colors,'where the resist color is obtained with vat dyes. It also relates to new resist printing pastes for the production of resist efiects on oxidation colors.
The oxidation colors comprise an important class oi dyestuffs which may be employed for the dyeing and printing of textile materials, such as natural and artificial cellulosic fibers, and natural silk. These colors upon oxidation in the presence of the fiber are converted to complex insoluble coloring matters. 'They include aromatic amino compounds, such as aniline and aminodiphenylamine, which are oxidizable to form black dyeings, and para phenylene diamine, meta amino cresol, diam'sidine, etc.', which are oxidizable to form fast brown colorations on textile materials. The oxidation colors also include the soluble leuco ester salts of vat dyes which upon oxidation in the presence of the fiber are productive of dyeings of various shades. All of these colors are developed (oxidized) on the fiber under acid conditions. Accordingly, the term oxidation colors, as used herein, denotes and includes colors which are applied directly to the material and then'developed by oxidation under acid conditions. A conventional method of applying oxidation colors to a textile material involves padding the textile material with a solution of the. desired oxidation color, drying the thus padded material, and then developing the color by a procedure including aging and steaming,
\ and, if desired or necessary, passing the material through an acid. bath containing an oxidizing agent.
It is known that white effects on oxidation colors may be obtained by applying locally to a textile material which is impregnated withia solution of an oxidation color, a paste containing an' production of effects on oxidation colors. These procedures have several disadvantages. For example, the use of colored printing pastes which are composed of vat dyes and the conventional alkaline reacting substances is characterized by a number of draw-backs which are due to the extremelyhygroscopic properties of these alkaline substances: for, during the development process the said hygroscopic substances cause the colored paste after it is applied by printing to the textile material to flush and to form an irregular white outline around the print and thereby to spoil the desired effect. Instead of the conventionalalkaline substances, alkylol-monoamines have been used, but they are not entirely satisfactory because they are relatively weakly alkaline and to obtain suflicient alkalinity they must be used in large proportions. Further, these compounds are liquids which have a tendency to spread, and the prints obtained with pastes containing them tend to be sticky and to mark-off.
The efiects produced by practicing the above procedures may be termed either reserve effects or resist efiects. However, inasmuch. as the ac,-
tion of the pastes applied .to selected areas of the materials is to resist the development of the ground colors, for simplicity in terminology, effects .of this type are referred to herein as duction of the eflects are termed resist pastes.
It is a principal object of the present invention to provide a process for the production of superior white and colored resist styles on oxidation colors. A further object of the-invention is to provide a process for the production of colored resist styles on oxidation colors, the said styles being obtained with the use of resist printing pastes containing vat dyes.
A further object of the invention is to provide novel white and colored resistprinting pastes which are adapted for use in the production of resist styles with oxidation colors. i
Other objects of the invention in part will be obvious and in part will appear hereinafter.
It has been found in accordance with the present invention that by incorporating in white and colored resist printing pastes-certain hydroxylated aliphatic polyamines, describQmore fully hereinafter, resist printing pastes are produced which, when employed in place of the conventional resist printing pastes in the productionof white and colored resist efiects on ground colorations obtained with oxidation colors, are productive of efiects which are clearly outlined and are substantially free from undesirable fiushing.
' resist efiects. Also, the pastes used'in the pro- In accordance with a more specific aspect of the present invention it has been found that colored resist efiects on oxidation colors may be obtained with particularly satisfactory results by employing resist printing pastes containing a vat dye and a hydroxylated aliphatic polyamine of the type described below. Such colored resist pastes have been found to produce effects which are well penetrated into the material and are characterized by exceptional brilliance.
The hydroxylated aliphatic polyamines employed in the resist printing pastes of the invention are aliphatic polyamines in which the amino groups may be unsubstituted, but at least one amino group preferably contains as a substituent at least one alkyl or aralkyl radical. (In referring to an alkyl radical herein, it will be understood that cyclic alkyl as well as chain alkyl radicals are intended.) The central radical of these compounds is an aliphatic radical which may consist of a single alkyl radical or a plurality of alkyl radicals linked together by a non-carbon atom or group, such as, for example, 0, f5, and NXs, wherein X5 represents hydrogen, alkyl, aralkyl, or hydroxyalkyl. Throughout this specification and claims the term "non-carbon linkages denotes O, S and NX5 as herein defined. The compounds contain at least one hydroxyl group which may be in the central aliphatic radical, or in an N-alkyl radical, or both. Thus, the hydroxylated aliphatic polyamines may be represented by the following general formula:
wherein R represents an alkyl radical or a radical consisting of a plurality of alkyl radicals linked together by non-carbon atoms or groups such as O, S, and NXs, (wherein. X5 has the above meaning); X1, X2, IQ, and X4 each represents hydrogen, an alkyl radical, an aralkyl radical, a hydroxyalkyl radical, or two of the X's of X1, X2, X1, X4 joined to different nitrogen atoms conjointly represent a bivalent alkyl radical; and n .represents a small whole number. In cases where the radical represented by R is free from hydroxyl groups, at least one of X1, X2, X3, and X4 represents a 'hydroxyalkyl radical. It is preferred to employ compounds in which the amino groups are substituted by at least one and prefererably by two or more hydroxyalkyl radicals, regardless of whether the radical represented by R contains hydroxyl groups.
As above indicated, the radical represented by B may contain hydroxyl groups as substituents.
radical contains 1 to 3 ethylene groups which, in cases where this radical contains more than one ethylene group, are linked together by O, S, or NXs, X5 having the above meaning. Further, the preferred compounds contain at least one, and preferably two or more, hydroxyethyl radicals as substituents in the amino groups.
The lower carbon chain compounds of ,the above type have low melting points, and are viscous liquids at ordinary temperatures; the viscosity of the compounds increasing with increase in their molecular weight. The high molecular chain compounds, on the otherhand, are crystalline or amorphous solids which melt above 50 C. All of the compounds of the above type are of low volatility and possess high solubility in water, alcohol, and in most organic solvents.
The hydroxylated aliphatic polyamines of the above type are further characterized by an exceedingly strong alkaline character. The superior prints obtainable by the process of the present invention are probably due in great measure'to the fact that because of the exceedingly high basic character of the hydroxylated aliphatic polyamines the amount of alkaline reacting substances used in the preparation of resist printing It will also be understood that this radical may contain other substituents which do not alter the essential characteristics of the compounds, such as, for example, alkoxy or aralkyloxy radicals. Further, it will be understood that the alkyl and aralkyl radicals attached to the amino groups of the compounds may contain substituents, especially hydroxyl groups. In this connection itshould be noted that where an N-aralkyl,
radical contains two or more carbon atoms in the alkyl radical thereof and this alkyl radical contains hydroxyl groups as substituents, it is regarded as a hydroxyalkyl radical for the purposes of this invention.
Among the compounds of the above class, those which are generally preferred for use in the re--, sist pastes of the invention are hydroxylated aliphatic diamines in which the central aliphatic pastes may be lowered to a relatively small quantity which by virtue of its paucity avoids the flushing and spreading of the printed surface while at the same time it efiiciently inhibits the development of the oxidation color employed as the ground shade. Further, when used in resist pastes containing vat dyes, the hydroxylated aliphatic polyamines exert solubilizing action on the leuco vat dyes which assists in causing them to penetrate. the fiber, thereby producing superior prints. The compounds of the above class which are solids are valuable because printed areas containing them, on being dried out, are free from stickiness.
It will be understood that any one or a mixture of a wide variety of hydroxylated aliphatic polyamines which contain at least one N-alkyl group containing at least two carbon atoms and at least one hydroxyl group may be employed in the preparation of the resist printing pastes of the present'invention. Among such polyamines may be mentioned the following compounds:
1,2-di- (2'-ethanolaminoethane 1,2-bis- (di-Z' -ethanolamino-) ethane 1100111011, omomoH N-CHaCH -N Hocmom omomon 1 ,2-di- (2,3'-propandiol-amino-) ethane 0H 0H no omoHoHr-Nir-o mom-macmr'lnomon di- (2',3'-propandiol-2-amino-ethyl-) ether 1 onionr-nn-onzononomon cH.cH:NH-on,o11orrcmo11 1,
CH2(CHOH) 4CH2OH 1,2-di- (4'-cyclohexanol-amino-)ethane oar-on; car-on, HO CH-NH-CHaCHz-NH-C onon orb-ch, om-o di-(N-4'-cyclohexanol-2-amino-ethyl-)ether CHr-CH:
onon CHi-Cl CHECK:
onon CHr-C a di- (ethanolaniino-ethyl-) sulfide omomNn-cmomon CHaCHr-NH-C -C HaOHr-NH-CHQCHiOH I bis- (di-2'-ethanol-2-amino-ethylQsulfide CHaCHaOH CHICHt-N CHsUHaOH CH:CHrN
o m o m 0 H di- (2' ,3 '-propandlol- 2-amino-ethyl-) sulfide omcm-NH-cmcnoHcmoH s I \CH: CHr-NH-CHsCHOHCHzOH N N diethanol -trimethylene-tetramine CHaCIEhOH N N -triethanol-trimethy1ene-tetramine 49 no onion,
CH2NHCH:NHCH:NHCH:CHxOH HOCHiC 8 g N N -tetraethanol-trimethylene tetramine Hoorncm onlomon CH:NHCHzNHCHr-NH nocmo I onlcnlon N N -bis-diethanol-N=-ethanol-trimethylene tetramine The resist printing pastes of the present invention may be prepared in a simple manner. For example, toprepare resist printing pastes for the production of white resist effects on oxidation colors, there may be added to the usual thicken- 75 in the usual manner with the following solution ing ingredients of such pastes one or a mixture of the hydroxylated aliphatic polyamines of the above type. White resist eifects on oxidation colors may be obtained .in accordance with the present invention by applying this resist printing paste in the conventional manner to a fabric which has been prepared with a. composition containing the oxidation color desired for the ground shade. Thereafter, the-textile material is subjected to a conventional developing treatment whereupon a white resist effect is obtained on the developed ground; This development treatment may include merely a steaming and aging procedure where that is sufliclent to oxidize the ground color (which has been applied tothe materialin a solution containing an oxidizing agent). It may include, however, an acid aging or, after the usual steaming and aging, a passage of the material through an oxidizing bath containing an oxidizing agent and an acid.
In order for the invention to be more fully understood, reference should be had to the following examples in which are described resist printing pastes and processes by which 'white resist effects may be obtained on oxidation colors. It will be understood, however,,that the invention is in no way limited to the specific proportions and procedures described in the examples. The parts are by weight.
Example 1.White cotton material is prepared for aniline black:
48 parts sodium chlorate- 115 parts sodium ferrocyanide 144 parts aniline hydrochloride dissolved in 2000 partswater.
The cloth is padded therewith, then dried and printed with the following white resist printing paste:
400 parts British gum (powder) 500 parts water,-to which 100 parts 1,2 -bis-(di-2' -ethanol-amino-) ethane are added.
After printing,- the material is steamed for about 2 minutes at 102 0., in arapid ager, then passed into an oxidation bath composed of /2 per cent sodium bichromate and 1 per centof a 28 0 per cent solution of' acetic acid. The printed material is then rinsed, soaped, rinsed, and dried. A white resist print is thus obtained on the aniline black ground.
Example 2.-A,white resist printing effect on a fast brown ground may be obtained as follows:
A white cotton and rayon mixed fabric is prepared with a padding liquor which is made by mixing the following three solutions:
(l) 20 parts Fuscamine G (meta amino phenol). 20 parts hydrochloric acid 20 B. are dissolved in 400 parts water by applying heat. (2) 25 parts sodium chlorate parts hot water (3) 5 parts sodium ferrocyanide 100 parts water.
These solutions are mixed cold and standardized to 1000 parts total. r i
- After padding, the fabric is dried, preferably in hot air and then printed with the resist paste described in Example 1. f After printing, the ma terial is passed through a rapid ager for about 5 to 10 miflutes at 105 C. The fabric may then be subjected to ammonia vapors or may be rinsed immediately after steaming in luke warm water, soaped, rinsed and dried.
Example 3.-A natural silk fabric is padded with the following padding liquor:
From 15 to 20 parts Ortamine D (ortho dianisidine) are dissolved in from 15 to 20 parts acetine and from 3.75 to parts hydrochloric acid 20 B., and
from 8 to 12 parts formic acid 90%, to which solution from 15 to 20 parts sodium chlorate and from 5 to 8 parts sodium ferrocyanide are added.
The whole is standardized to 1000 parts total.
The silk material is then printed with a white resist paste composed of: e
7'75 parts gum Senegal, 1:1 100 parts sodium acetate 50 parts potassium sulfite solution 45 B. '75 parts glyceryl diethanol-ethylene diamine.
After printing, the material is steamed for about 5 minutes whereby the brown ground shade'is developed and the fabric is passed into tepid water, rinsed thoroughly, soaped, rinsed and dried. Thus, a white resist effect is obtained on a brown bottom shade.
Colored resist efiects on oxidation colors may be obtained in accordance with the present invention with the use of printing pastes containing dyes of various types, it being only necessary that such dyes be applicable to a textile material in an alkaline paste. For example, colored resist effects may be obtained with the use of resist printing pastes containing dyes, such as vat dyes, sulfur dyes, and azoic printing compositions (e. g., nitrosamine and diazo-amino compositions). The present invention, however, is particularly directed to the production of. resist printing pastes containing vat dyes and the above-described hydroxylated aliphatic polyamines. Such resist printing pastes have been found to yield excellent results particularly when employed on materials composed of cellulosic or natural, silk fibers. Vat dye resist printing pastes may be prepared in accordance with the present invention by incorporating with the usual components of a vat dye printing paste (which ordinarily include a vat dye in the unreduced form, thickening ingredients, a reducing agent, such as sodium formaldehyde sulfoxylate, an alkali carbonate or caustic alkali, and dispersing agents, and other suitable additions) a hydroxylated aliphatic polyamine of the type already described. The total amount of alkaline material ordinarily employed in such printing pastes, however, may be reduced in most cases to a minimum because of the strongly basic character of the hydroxylated aliphatic polyamine.
Colored resist efiects may be obtained on oxidation color ground dyeings in accordance with the present invention by locally applying\ a vat dye resist printing paste of the above type to a textile material which has been previously prepared with a grounding liquor containing an oxidation color, and then subjecting the material to a development treatment. The following examples are illustrative'of procedures carried out in accordance. with the present invention wherein colored resist effects are obtained with vat dyes on ground shades of oxidation colors. The parts are by weight:
Example st-Cotton material is prepared with the aniline black padding solution described in Example 1, and is then printed with the following vat dye composition:
Parts British gum (powder) 250 Water 275 Vat Brilliant Indigo 4Br paste (tetra-brom- The printed material'is then passed through a rapid ager for about 4 minutes and oxidized in the usual way, washed and dried; thus, a blue resist effect is obtained on a black ground.
Example 5.Cotton material is padded with the following solution and then dried.
30 parts of the disodium salt of the sulfuric leuco ester represented by the following formula:
S OaNB I CH: (lJ I S OaNa Parts Diethylene glycol 30, Water 865 Sodium nitrite 15 Ammonia solution 25% s 10 Gum tragacanth 25% 1 50 made up to 1000 parts by volume.
' Printing color 200 parts National Vat'Orange R (Color Index 1217) are mixed intimately into:
720 parts of a thickening composed of: a
520 parts of corn starch British gum thickening 150 parts of potassium carbonate 120 parts of sodium formaldehyde sulfoxylate 50 parts of glycerine 160 parts water and parts of di(N-butyl-N ethanol-amino-) ethane or 1,2-di-glucamino-ethane.
After printing and drying, the material is passed through a vat dye ager for about 4 to 5 minutes, whereby the printed Vat Orange R is developed; thereafter, the material may be passed for about 3 to5'minutes into an acid ager which will cause the ground shade to be developed, but not in the areas where the resist has been applied by the printing. Instead-of devel. oping the ground shade in an acid ager, it may be developed by padding the material with a solution containing per '1000 parts:
. Parts Oxalic acid 10 Formic acid 10 Glauber salt 25 and directly thereafter drying the padded material on a cylinder drying machine. The fabric is then rinsed and soaped for 10 minutes at the boil, rinsed, dried and finished in the usual way.
A very fast and brilliant orange print is thus obtained on a dyed vat blue ground shade. The general procedure described in the above example may be used for the preparation of white resists on ground colorations obtained with leuco ester salts of vat dyes by using in place of the vat dye resist printing paste the white resist printing pastes described in Examples 1 and 3. In this case the development is similar to that described in Example 5, being carried out by subjecting the material to an acid aging treatment or padding it with the acid padding liquor illustrated above.
.While in the above examples there havebeen specifically illustrated procedures in which only white or colored resist effects are obtained on oxidation colors, it will be understood that byapplying white and colored resist printing pastes simultaneously to a textile material; which has been impregnated with a grounding liquor of an oxidation color, combined white and multi-colored resist effects may be obtained. Also, it is be obtained with the use of dyes other than vat dyes applicable to textile materials in alkaline pastes, and that multi-colored resist effects may be obtained by applying simultaneouslytwo or.
paste containing an azoicprinting composition.
My application S erial No. 242,746, filed of even date herewith, is'directed to the "production of resist printing pastes containing azoic dye compositions and to' a process for the production of For example,
colored resist effects on ground colorations of oxidation colors obtained with the use of such resist printing pastes. I
In the preparation of colored resist effects on ground colorations obtained with oxidation colors, it will be obvious that any suitable vat dye may be employed in place of the vat dyes specifically mentioned in the above Examples 4 and 5. For example, in the production of colored resist efiects in accordance with the process of the present invention, there may employed a vat dye selected from the following group:
1 Color Index No.
'Carbanthrene Blue GCD 1113 Carbanthrene Yellow G double powder 1118 Carbanthrene Golden Orange 2RT powder- 1097 Carbanthrene Golden Orange G double powder 1096 Carbanthrene Blue Green FFB double powder 1173 Carbanthrene Violet 2R powder 1104 Carbanthrene Dark Blue DR. 1099 -Carbanthrene Flavine GC double powder--- 1095 Carbanthrene Red Violet ZRNX powder 1161 Carbanthrene Brilliant Green supra 1101 Brilliant Indigo 4G powder 1189 Brilliant Indigo 4B powder .(tetrabrom indigo) Vat Scarlet G paste 1128 Vat Brown G paste (dinaphthyl-thioindigo) Vat Green G paste"; 1199 Vat VioletR paste 1222 It will be understood, of. course, that in the preparation of resist printing pastes in accordance with the procedures described in the foregoing examples, the hydroxylated aliphatic polyamines employed therein may be replaced by any one or a mixture of other hydroxylated alifor example, one or a mixture of those specifically mentioned.
The proportions of ingredients specified for preparation of the resist printing pastes in the foregoing examples may be varied within wide limits. As noted above, by the use of the hydroxylated aliphatic polyamines in resist printing pastes the total amount of alkaline materials in the pastes may be reduced to a minimum. In some instances, as in the production of white resist effects, one or more of the hydroxylated ali-' phatic polyamines may be used in place of the entire amount of alkali normally used in pastes for the production of resist effects of this type. In other instances, superior results are obtained by replacing only a part of the alkali normally used with one or more of the amines. For best results, it is preferred to employ one or more of the amines in place of at least a part of the alkali normally used; i.'e., they are used as alkaline agents. It will be understood that the'particular proportions to be employed in any given case are dependent upon the character of the textile material employed, the type of effect desired, and the kind of development treatment. Hence, these proportions may be left largely to the'dlscretion of the operator. The foregoing examples, however, are illustrative oftypical procedures and may be referred to as a basis for comparison.
it is preferred to produce. the resist effects by applying the resist pastes to a material impregnated with a ground color,the invention is not limited to this manner of proceeding since the resist pastes may be applied to the material before impregnation with the ground color.
" Since certain changes may be made in the above compositions and processes without deabove description should be taken and not in. a limiting sense.
I claim:
1. A resist printing paste for the production of resist eflects on oxidation colors comprising a thickener and a hydroxylated aliphatic polyamine free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals.
2. A resist printing paste for the production of colored resist effects on oxidation colors comprising a dye applicable to textile materials in an alkaline paste, a thickener, and a hydroxylated aliphatic polyamine free from amino substituents other than alkyl radicals, aralkyl radicals, and hydroxyalkyl radicals.
3. A resist printing paste for the production of resist effects on oxidation colors comprising a thickener and a hydroxylated aliphatic polyamine having as a central radical a plurality of alkyl radicals linked together by non-carbon linkages, said polyamine being free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals and containing at least one hydroxyalkyl radical as an amino-substituent when the'central radical is free from hydroxyl groups. 7
v 4. A resist printing paste for the production of colored resist effects on oxidation colors comprising a dye applicable to textile-materials in an alkaline paste, a thickener, and a hydroxylated aliphatic polyamine having as a central radical as illustrative a plurality ofallwl radicals linked together, by
phatic polyamines of the class disclosed above; cals, aralkyl radicals and-hydroxyalkyl radicals Although, as indicated in the above examples,
5. A resist printing paste tor the production ofcolored resist efiects on oxidation colors-comprising an unreduced vat dye, a reducing agent. a
thickener, and a hydroxylated aliphatic poly-,
amine having as a central radical a plurality of alkyl radicals linked together by non-carbon linkages, said polyamine being free from amino-ubstituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals and containing at least one hydroxy-allwl radical as an amino-substituent when the central radical is free from hydroxyl groups.
6. A resist printing paste for the production of resist effects on oxidation colors comprising a thickener and a hydroxyalkylated ethylenediamine which contains at least one hydroxyalkyl radical as an amino-substituent and which is free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals.
7. A resist printing paste for the production of colored resist efiects on oxidation colors comprising an unreduced vat dye, a thickener, and a hydroxyalkylated ethylenediamine which contains at least one hydroxyalkyl radical as an amino-substituent and which is free from aminosubstituents other than alkyl radicaIs araIkyI radicals and hydroxyalkyl radicals. Y
8. In the process of producing colored resist efiects on oxidation colors, the improvementwhich comprises applying to selected areas of a textile material impregnated with an undeveloped oxidation color a resist printing paste comprising a dye applicable to textile materials in an alkaline paste, a thickener, and a hydroxylated aliphatic polyamine free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals.
9. In the process of producing colored resist eflects on oxidation colors involving the step of applying to a textile material in selected areas a printing paste adapted to prevent the oxidation of the oxidation color, the improvement which comprises applying to a textile material impregnated with an undeveloped oxidation color a printing paste comprising an umeduced vat dye,
a reducing agent, a thickener, and a hydroxylated aliphatic polyamine having as a central radical a plurality of alkyl radicals linked together by non-carbon linkages, said polyamine being free from amino-substituents other than alkyl radicals, aralkyl radicals and hydroxyalkyl radicals and containing at least one hydroxyalkyl radical as an amino-substituent when the central radical is free from hydroxyl groups.
10. In the process of producing resist efiects on oxidation colors, the improvement which comprises applying to selected areas of a textile maradical as an amino-substituent and which is terial impregnated with an undeveloped oxidation color a resist printing paste comprising a thickener and a hydroxyalkylated ethylenediamine which contains at least one hydroxyalkyl free from amino-substituents other than alkyl radicals, araikyl radicals and hydroxyalkyl radi- 11. A resist printing paste for the production of resist effects on oxidation colors comprising a thickener and 1,2-bis- (di-Zf-ethanol-amino) ethane.
12. .A resist printing paste for the production of resist eflects on oxidation colors comprising a thickener and bis-(di-2',3'-propan-diol-2-aminoethyl) ether.
13, A resist printing paste for the production of resist eflects on oxidation colors comprising a thickener and bis -(di 2'- ethanol 2 aminoethyl-) sulfide.
- JEAN G. KERN.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US242745A US2256809A (en) | 1938-11-28 | 1938-11-28 | Production of resist effects |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US242745A US2256809A (en) | 1938-11-28 | 1938-11-28 | Production of resist effects |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2256809A true US2256809A (en) | 1941-09-23 |
Family
ID=22916018
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US242745A Expired - Lifetime US2256809A (en) | 1938-11-28 | 1938-11-28 | Production of resist effects |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2256809A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0055694A3 (en) * | 1980-12-30 | 1983-01-19 | Ciba-Geigy Ag | Vat and sulphur dyestuff preparations |
-
1938
- 1938-11-28 US US242745A patent/US2256809A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0055694A3 (en) * | 1980-12-30 | 1983-01-19 | Ciba-Geigy Ag | Vat and sulphur dyestuff preparations |
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