DE122686C - - Google Patents

Info

Publication number

DE122686C

DE122686C DENDAT122686D DE122686DA DE122686C DE 122686 C DE122686 C DE 122686C DE NDAT122686 D DENDAT122686 D DE NDAT122686D DE 122686D A DE122686D A DE 122686DA DE 122686 C DE122686 C DE 122686C

Authority

DE

Germany

Prior art keywords

black

acid

dyes

wool

diazotized

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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• 239000000975 dye Substances 0.000 claims description 36
• 239000002253 acid Substances 0.000 claims description 12
• 210000002268 wool Anatomy 0.000 claims description 8
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 6
• 238000004043 dyeing Methods 0.000 claims description 6
• NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 claims description 6
• OXNIZHLAWKMVMX-UHFFFAOYSA-N picric acid Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-N 0.000 claims description 4
• CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 2
• 125000000217 alkyl group Chemical group 0.000 claims 1
• 238000000034 method Methods 0.000 claims 1
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
• 238000004040 coloring Methods 0.000 description 7
• 235000008317 Condalia obovata Nutrition 0.000 description 5
• 244000147935 Condalia obovata Species 0.000 description 5
• 125000003368 amide group Chemical group 0.000 description 4
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 4
• 239000010446 mirabilite Substances 0.000 description 4
• RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 4
• VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
• 229910052804 chromium Inorganic materials 0.000 description 3
• 239000011651 chromium Substances 0.000 description 3
• 239000004744 fabric Substances 0.000 description 3
• CTIQLGJVGNGFEW-UHFFFAOYSA-L naphthol yellow S Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C([O-])=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 CTIQLGJVGNGFEW-UHFFFAOYSA-L 0.000 description 3
• 238000009971 piece dyeing Methods 0.000 description 3
• 239000000047 product Substances 0.000 description 3
• 150000003460 sulfonic acids Chemical class 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
• 240000007829 Haematoxylum campechianum Species 0.000 description 2
• RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 2
• 238000009835 boiling Methods 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 239000003973 paint Substances 0.000 description 2
• 238000010186 staining Methods 0.000 description 2
• JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
• IWOSIGNANKUKIQ-UHFFFAOYSA-N 3-[(4-aminophenyl)diazenyl]-4,5-dihydroxynaphthalene-2,7-disulfonic acid Chemical compound Nc1ccc(cc1)N=Nc1c(O)c2c(O)cc(cc2cc1S(O)(=O)=O)S(O)(=O)=O IWOSIGNANKUKIQ-UHFFFAOYSA-N 0.000 description 1
• RXERRVKLABZRCU-UHFFFAOYSA-N 4-acetamido-5-hydroxy-6-[[7-sulfo-4-[(4-sulfophenyl)diazenyl]naphthalen-1-yl]diazenyl]naphthalene-1,7-disulfonic acid Chemical compound CC(=O)Nc1ccc(c2cc(c(N=Nc3ccc(N=Nc4ccc(cc4)S(O)(=O)=O)c4ccc(cc34)S(O)(=O)=O)c(O)c12)S(O)(=O)=O)S(O)(=O)=O RXERRVKLABZRCU-UHFFFAOYSA-N 0.000 description 1
• 208000006558 Dental Calculus Diseases 0.000 description 1
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
• 230000029936 alkylation Effects 0.000 description 1
• 238000005804 alkylation reaction Methods 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• -1 azo acid blue B Chemical compound 0.000 description 1
• 230000003796 beauty Effects 0.000 description 1
• 235000012709 brilliant black BN Nutrition 0.000 description 1
• 150000001735 carboxylic acids Chemical class 0.000 description 1
• 230000008878 coupling Effects 0.000 description 1
• 238000010168 coupling process Methods 0.000 description 1
• 238000005859 coupling reaction Methods 0.000 description 1
• 229910003460 diamond Inorganic materials 0.000 description 1
• 239000010432 diamond Substances 0.000 description 1
• 150000008049 diazo compounds Chemical class 0.000 description 1
• 229910052736 halogen Inorganic materials 0.000 description 1
• 150000002367 halogens Chemical class 0.000 description 1
• 235000019239 indanthrene blue RS Nutrition 0.000 description 1
• 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 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 125000001624 naphthyl group Chemical group 0.000 description 1
• ZHCUAFHZHYUGTO-UHFFFAOYSA-N sodium 4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonic acid Chemical compound C1=CC=C(C=C1)N=NC2=C(C3=C(C(=C(C=C3C=C2S(=O)(=O)O)S(=O)(=O)O)N=NC4=CC=C(C=C4)[N+](=O)[O-])N)O.[Na+] ZHCUAFHZHYUGTO-UHFFFAOYSA-N 0.000 description 1
• 238000007447 staining method Methods 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 239000013589 supplement Substances 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
• GKXVJHDEWHKBFH-UHFFFAOYSA-N xylylenediamine group Chemical group C=1(C(=CC=CC1)CN)CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1