BE624201A - - Google Patents

Info

Publication number

BE624201A

BE624201A BE624201DA BE624201A BE 624201 A BE624201 A BE 624201A BE 624201D A BE624201D A BE 624201DA BE 624201 A BE624201 A BE 624201A

Authority

BE

Belgium

Prior art keywords

parts

dye

phosphoric

product

aldehyde

Prior art date

Links

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• 239000000975 dye Substances 0.000 description 13
• 239000000047 product Substances 0.000 description 12
• 229920000742 Cotton Polymers 0.000 description 10
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
• NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 8
• 238000001816 cooling Methods 0.000 description 7
• 239000007795 chemical reaction product Substances 0.000 description 6
• QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
• 239000002253 acid Substances 0.000 description 5
• 229910000147 aluminium phosphate Inorganic materials 0.000 description 4
• RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical group C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 3
• 240000007817 Olea europaea Species 0.000 description 3
• 238000009835 boiling Methods 0.000 description 3
• 238000002360 preparation method Methods 0.000 description 3
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
• 125000004442 acylamino group Chemical group 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
• 125000004429 atom Chemical group 0.000 description 2
• 125000005843 halogen group Chemical group 0.000 description 2
• GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 2
• -1 nitro, amino Chemical group 0.000 description 2
• 238000003756 stirring Methods 0.000 description 2
• VZAMYPINYMMSGD-UHFFFAOYSA-N 9,10-dioxoanthracene-1-carbaldehyde Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2C=O VZAMYPINYMMSGD-UHFFFAOYSA-N 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
• ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
• 241000594011 Leuciscus leuciscus Species 0.000 description 1
• YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 1
• XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
• 150000001299 aldehydes Chemical class 0.000 description 1
• 239000004202 carbamide Substances 0.000 description 1
• 229910052801 chlorine Inorganic materials 0.000 description 1
• 239000000460 chlorine Substances 0.000 description 1
• 238000004040 coloring Methods 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000010586 diagram Methods 0.000 description 1
• OUMFRZJDHOKSPJ-UHFFFAOYSA-N dimethylaminophosphonic acid Chemical compound CN(C)P(O)(O)=O OUMFRZJDHOKSPJ-UHFFFAOYSA-N 0.000 description 1
• 125000004119 disulfanediyl group Chemical group *SS* 0.000 description 1
• OAEGRYMCJYIXQT-UHFFFAOYSA-N dithiooxamide Chemical compound NC(=S)C(N)=S OAEGRYMCJYIXQT-UHFFFAOYSA-N 0.000 description 1
• 150000002500 ions Chemical class 0.000 description 1
• 238000000034 method Methods 0.000 description 1
• 239000000203 mixture Substances 0.000 description 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
• PTMHPRAIXMAOOB-UHFFFAOYSA-L phosphoramidate Chemical compound NP([O-])([O-])=O PTMHPRAIXMAOOB-UHFFFAOYSA-L 0.000 description 1
• 239000000049 pigment Substances 0.000 description 1
• 239000002798 polar solvent Substances 0.000 description 1
• FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical group [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
• HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
• 229910000029 sodium carbonate Inorganic materials 0.000 description 1
• 239000002689 soil Substances 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 230000002459 sustained effect Effects 0.000 description 1
• 238000005406 washing Methods 0.000 description 1