DE180727C - - Google Patents

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Publication number

DE180727C

DE180727C DENDAT180727D DE180727DA DE180727C DE 180727 C DE180727 C DE 180727C DE NDAT180727 D DENDAT180727 D DE NDAT180727D DE 180727D A DE180727D A DE 180727DA DE 180727 C DE180727 C DE 180727C

Authority

DE

Germany

Prior art keywords

etching

naphthylamine

white

dyeings

etch

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.)

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• 238000005530 etching Methods 0.000 claims description 20
• 238000000034 method Methods 0.000 claims description 7
• 239000000975 dye Substances 0.000 claims description 6
• JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 claims description 5
• 238000004043 dyeing Methods 0.000 claims description 5
• 239000000835 fiber Substances 0.000 claims description 4
• -1 o-aminocresol benzyl ether Chemical compound 0.000 claims description 4
• HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 3
• 150000001875 compounds Chemical class 0.000 claims description 3
• YGOFNNAZFZYNIX-UHFFFAOYSA-N 3-N-phenylbenzene-1,2,3-triamine Chemical compound NC=1C(=C(C=CC1)NC1=CC=CC=C1)N YGOFNNAZFZYNIX-UHFFFAOYSA-N 0.000 claims description 2
• KLZPLKQRIOMCLB-UHFFFAOYSA-N 4-(2-nitroethoxy)aniline Chemical compound NC1=CC=C(OCC[N+]([O-])=O)C=C1 KLZPLKQRIOMCLB-UHFFFAOYSA-N 0.000 claims description 2
• XWPDPFLBSAPRCO-UHFFFAOYSA-N 4-(chloromethoxy)aniline Chemical compound NC1=CC=C(OCCl)C=C1 XWPDPFLBSAPRCO-UHFFFAOYSA-N 0.000 claims description 2
• IWRVPXDHSLTIOC-UHFFFAOYSA-N 4-phenyldiazenylbenzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1N=NC1=CC=CC=C1 IWRVPXDHSLTIOC-UHFFFAOYSA-N 0.000 claims description 2
• 150000001298 alcohols Chemical class 0.000 claims description 2
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 2
• 238000004519 manufacturing process Methods 0.000 claims description 2
• 150000001299 aldehydes Chemical class 0.000 claims 1
• HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical class OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 claims 1
• 239000003086 colorant Substances 0.000 description 5
• GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 5
• WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
• GRWZHXKQBITJKP-UHFFFAOYSA-N dithionous acid Chemical class OS(=O)S(O)=O GRWZHXKQBITJKP-UHFFFAOYSA-N 0.000 description 3
• 239000000976 ink Substances 0.000 description 3
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
• RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
• PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
• XTGCLWKDGNDDCH-UHFFFAOYSA-N O=C.OS(=O)S(O)=O Chemical compound O=C.OS(=O)S(O)=O XTGCLWKDGNDDCH-UHFFFAOYSA-N 0.000 description 2
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
• 239000000987 azo dye Substances 0.000 description 2
• 238000013016 damping Methods 0.000 description 2
• 229940017705 formaldehyde sulfoxylate Drugs 0.000 description 2
• SBGKURINHGJRFN-UHFFFAOYSA-N hydroxymethanesulfinic acid Chemical compound OCS(O)=O SBGKURINHGJRFN-UHFFFAOYSA-N 0.000 description 2
• 235000018553 tannin Nutrition 0.000 description 2
• 229920001864 tannin Polymers 0.000 description 2
• 239000001648 tannin Substances 0.000 description 2
• 230000008719 thickening Effects 0.000 description 2
• KMZHZAAOEWVPSE-UHFFFAOYSA-N 2,3-dihydroxypropyl acetate Chemical compound CC(=O)OCC(O)CO KMZHZAAOEWVPSE-UHFFFAOYSA-N 0.000 description 1
• CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical class CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
• ADAOOVVYDLASGJ-UHFFFAOYSA-N 2,7,10-trimethylacridin-10-ium-3,6-diamine;chloride Chemical compound [Cl-].CC1=C(N)C=C2[N+](C)=C(C=C(C(C)=C3)N)C3=CC2=C1 ADAOOVVYDLASGJ-UHFFFAOYSA-N 0.000 description 1
• 102000009027 Albumins Human genes 0.000 description 1
• 108010088751 Albumins Proteins 0.000 description 1
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
• 229920002472 Starch Polymers 0.000 description 1
• 108010076830 Thionins Proteins 0.000 description 1
• 239000002253 acid Substances 0.000 description 1
• 150000007513 acids Chemical class 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 229910052787 antimony Inorganic materials 0.000 description 1
• WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
• 125000003118 aryl group Chemical group 0.000 description 1
• KSCQDDRPFHTIRL-UHFFFAOYSA-N auramine O Chemical compound [H+].[Cl-].C1=CC(N(C)C)=CC=C1C(=N)C1=CC=C(N(C)C)C=C1 KSCQDDRPFHTIRL-UHFFFAOYSA-N 0.000 description 1
• 239000000981 basic dye Substances 0.000 description 1
• 239000003518 caustics Substances 0.000 description 1
• WOTPFVNWMLFMFW-UHFFFAOYSA-N chembl1967257 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1 WOTPFVNWMLFMFW-UHFFFAOYSA-N 0.000 description 1
• CYZWPZHRSZNWLS-UHFFFAOYSA-N chembl1994043 Chemical compound C1=CC=C2C(N=NC3=C4C=CC=CC4=CC=C3O)=CC=CC2=C1 CYZWPZHRSZNWLS-UHFFFAOYSA-N 0.000 description 1
• 238000004040 coloring Methods 0.000 description 1
• 239000007859 condensation product Substances 0.000 description 1
• BBFBNDYGZBKPIA-UHFFFAOYSA-K dichlorozinc [7-(diethylamino)phenothiazin-3-ylidene]-dimethylazanium chloride Chemical compound [Cl-].Cl[Zn]Cl.C1=CC(=[N+](C)C)C=C2SC3=CC(N(CC)CC)=CC=C3N=C21 BBFBNDYGZBKPIA-UHFFFAOYSA-K 0.000 description 1
• 239000000982 direct dye Substances 0.000 description 1
• 238000001035 drying Methods 0.000 description 1
• 239000004744 fabric Substances 0.000 description 1
• QJQZEJFUIOWFMS-UHFFFAOYSA-N formaldehyde;sulfanediol Chemical compound O=C.OSO QJQZEJFUIOWFMS-UHFFFAOYSA-N 0.000 description 1
• 235000011187 glycerol Nutrition 0.000 description 1
• 229910052500 inorganic mineral Inorganic materials 0.000 description 1
• 159000000014 iron salts Chemical class 0.000 description 1
• 239000011707 mineral Substances 0.000 description 1
• 235000010755 mineral Nutrition 0.000 description 1
• 238000001556 precipitation Methods 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
• 235000011121 sodium hydroxide Nutrition 0.000 description 1
• 239000002562 thickening agent Substances 0.000 description 1
• ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
• 150000004992 toluidines Chemical class 0.000 description 1
• 229940100445 wheat starch Drugs 0.000 description 1