DE1469738A1 - Verfahren zum Faerben und Bedrucken von Polyolefinmaterialien - Google Patents
Verfahren zum Faerben und Bedrucken von PolyolefinmaterialienInfo
- Publication number
- DE1469738A1 DE1469738A1 DE19651469738 DE1469738A DE1469738A1 DE 1469738 A1 DE1469738 A1 DE 1469738A1 DE 19651469738 DE19651469738 DE 19651469738 DE 1469738 A DE1469738 A DE 1469738A DE 1469738 A1 DE1469738 A1 DE 1469738A1
- Authority
- DE
- Germany
- Prior art keywords
- hydrazine
- quinone
- heterocyclic
- temperatures
- materials
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims description 22
- 238000000034 method Methods 0.000 title claims description 22
- 229920000098 polyolefin Polymers 0.000 title claims description 5
- 238000004040 coloring Methods 0.000 title description 3
- -1 preferably threads Substances 0.000 claims description 41
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 29
- 239000004743 Polypropylene Substances 0.000 claims description 23
- 229920001155 polypropylene Polymers 0.000 claims description 23
- WOAHJDHKFWSLKE-UHFFFAOYSA-N 1,2-benzoquinone Chemical compound O=C1C=CC=CC1=O WOAHJDHKFWSLKE-UHFFFAOYSA-N 0.000 claims description 13
- 238000004043 dyeing Methods 0.000 claims description 11
- 239000004744 fabric Substances 0.000 claims description 11
- 239000002657 fibrous material Substances 0.000 claims description 9
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 239000003995 emulsifying agent Substances 0.000 claims description 7
- 239000000835 fiber Substances 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 150000002429 hydrazines Chemical class 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 239000007800 oxidant agent Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 claims 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 150000004780 naphthols Chemical class 0.000 claims 1
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 15
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 14
- 239000000203 mixture Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 229910052759 nickel Inorganic materials 0.000 description 8
- YYVYAPXYZVYDHN-UHFFFAOYSA-N 9,10-phenanthroquinone Chemical compound C1=CC=C2C(=O)C(=O)C3=CC=CC=C3C2=C1 YYVYAPXYZVYDHN-UHFFFAOYSA-N 0.000 description 7
- 150000002815 nickel Chemical class 0.000 description 6
- QDGHXQFTWKRQTG-UHFFFAOYSA-N pyrimidin-2-ylhydrazine Chemical compound NNC1=NC=CC=N1 QDGHXQFTWKRQTG-UHFFFAOYSA-N 0.000 description 6
- PUDOJOGZPSCHRY-UHFFFAOYSA-N (6-methoxy-1h-benzimidazol-2-yl)hydrazine Chemical compound COC1=CC=C2N=C(NN)NC2=C1 PUDOJOGZPSCHRY-UHFFFAOYSA-N 0.000 description 5
- AFPRJLBZLPBTPZ-UHFFFAOYSA-N acenaphthoquinone Chemical compound C1=CC(C(C2=O)=O)=C3C2=CC=CC3=C1 AFPRJLBZLPBTPZ-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- JYSUYJCLUODSLN-UHFFFAOYSA-N 1,3-benzothiazol-2-ylhydrazine Chemical compound C1=CC=C2SC(NN)=NC2=C1 JYSUYJCLUODSLN-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- 229920000151 polyglycol Polymers 0.000 description 4
- 239000010695 polyglycol Substances 0.000 description 4
- QAMZBKMFWQSHDV-UHFFFAOYSA-N (6-methoxy-1,3-benzothiazol-2-yl)hydrazine Chemical compound COC1=CC=C2N=C(NN)SC2=C1 QAMZBKMFWQSHDV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- GULVDPYLWVXKGC-UHFFFAOYSA-N quinoxalin-2-ylhydrazine Chemical compound C1=CC=CC2=NC(NN)=CN=C21 GULVDPYLWVXKGC-UHFFFAOYSA-N 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- WUKBRNKMQNEPAW-UHFFFAOYSA-N (4-methylpyrimidin-2-yl)hydrazine Chemical compound CC1=CC=NC(NN)=N1 WUKBRNKMQNEPAW-UHFFFAOYSA-N 0.000 description 2
- FXYQRYGWWZKUFV-UHFFFAOYSA-N (6-chloropyridazin-3-yl)hydrazine Chemical compound NNC1=CC=C(Cl)N=N1 FXYQRYGWWZKUFV-UHFFFAOYSA-N 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229950011260 betanaphthol Drugs 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000002816 nickel compounds Chemical class 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- RODNZCIFRICALV-UHFFFAOYSA-N (3-chloroquinoxalin-2-yl)hydrazine Chemical compound C1=CC=C2N=C(Cl)C(NN)=NC2=C1 RODNZCIFRICALV-UHFFFAOYSA-N 0.000 description 1
- IRZALWDJCUHVNE-UHFFFAOYSA-N (3-methylpyridin-2-yl)hydrazine Chemical compound CC1=CC=CN=C1NN IRZALWDJCUHVNE-UHFFFAOYSA-N 0.000 description 1
- VXFWYILDQLZFDA-UHFFFAOYSA-N (4,5-dimethyl-1,3-thiazol-2-yl)hydrazine Chemical compound CC=1N=C(NN)SC=1C VXFWYILDQLZFDA-UHFFFAOYSA-N 0.000 description 1
- UVIIKLIUTUENOC-UHFFFAOYSA-N (4,5-dimethyl-1h-imidazol-2-yl)hydrazine Chemical compound CC=1N=C(NN)NC=1C UVIIKLIUTUENOC-UHFFFAOYSA-N 0.000 description 1
- RSRDFWTZMTVOGB-UHFFFAOYSA-N (4,6-diphenyl-1,3,5-triazin-2-yl)hydrazine Chemical compound N=1C(NN)=NC(C=2C=CC=CC=2)=NC=1C1=CC=CC=C1 RSRDFWTZMTVOGB-UHFFFAOYSA-N 0.000 description 1
- MDWOPAZAWVQNLN-UHFFFAOYSA-N (4-methoxy-6-methyl-1,3,5-triazin-2-yl)hydrazine Chemical compound COC1=NC(C)=NC(NN)=N1 MDWOPAZAWVQNLN-UHFFFAOYSA-N 0.000 description 1
- HXQPYFMXCAIHAB-UHFFFAOYSA-N (4-methoxypyrimidin-2-yl)hydrazine Chemical compound COC1=CC=NC(NN)=N1 HXQPYFMXCAIHAB-UHFFFAOYSA-N 0.000 description 1
- FLDYBLAUDDQRAB-UHFFFAOYSA-N (4-methylquinolin-2-yl)hydrazine Chemical compound C1=CC=C2C(C)=CC(NN)=NC2=C1 FLDYBLAUDDQRAB-UHFFFAOYSA-N 0.000 description 1
- VTOUNUQLXMNNMQ-UHFFFAOYSA-N (4-phenyl-2-thiazolyl)hydrazine Chemical compound S1C(NN)=NC(C=2C=CC=CC=2)=C1 VTOUNUQLXMNNMQ-UHFFFAOYSA-N 0.000 description 1
- BJYYJTBSIMBZTC-UHFFFAOYSA-N (4-phenylpyrimidin-2-yl)hydrazine Chemical compound NNC1=NC=CC(C=2C=CC=CC=2)=N1 BJYYJTBSIMBZTC-UHFFFAOYSA-N 0.000 description 1
- WUDNSGDMTFEQIF-UHFFFAOYSA-N (5-chloropyrimidin-2-yl)hydrazine Chemical compound NNC1=NC=C(Cl)C=N1 WUDNSGDMTFEQIF-UHFFFAOYSA-N 0.000 description 1
- FTYUJXNPXVDGLD-UHFFFAOYSA-N (5-methoxypyrimidin-2-yl)hydrazine Chemical compound COC1=CN=C(NN)N=C1 FTYUJXNPXVDGLD-UHFFFAOYSA-N 0.000 description 1
- LMFJCTVBDCMPAI-UHFFFAOYSA-N (5-phenylpyrimidin-2-yl)hydrazine Chemical compound C1=NC(NN)=NC=C1C1=CC=CC=C1 LMFJCTVBDCMPAI-UHFFFAOYSA-N 0.000 description 1
- VEYRIFLVMZFSLK-UHFFFAOYSA-N 1,3-benzothiazole;1h-indole-2,3-dione Chemical compound C1=CC=C2SC=NC2=C1.C1=CC=C2C(=O)C(=O)NC2=C1 VEYRIFLVMZFSLK-UHFFFAOYSA-N 0.000 description 1
- QITJGSMHKVXOFR-UHFFFAOYSA-N 1,3-benzoxazol-2-ylhydrazine Chemical compound C1=CC=C2OC(NN)=NC2=C1 QITJGSMHKVXOFR-UHFFFAOYSA-N 0.000 description 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- FHMMQQXRSYSWCM-UHFFFAOYSA-N 1-aminonaphthalen-2-ol Chemical class C1=CC=C2C(N)=C(O)C=CC2=C1 FHMMQQXRSYSWCM-UHFFFAOYSA-N 0.000 description 1
- VCYBVWFTGAZHGH-UHFFFAOYSA-N 1-methylindole-2,3-dione Chemical compound C1=CC=C2N(C)C(=O)C(=O)C2=C1 VCYBVWFTGAZHGH-UHFFFAOYSA-N 0.000 description 1
- 150000004782 1-naphthols Chemical class 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- PXUYWNZBZXDJEU-UHFFFAOYSA-N 1h-benzimidazol-2-ylhydrazine Chemical compound C1=CC=C2NC(NN)=NC2=C1 PXUYWNZBZXDJEU-UHFFFAOYSA-N 0.000 description 1
- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical class C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 description 1
- 150000004786 2-naphthols Chemical class 0.000 description 1
- KNAXWOBOCVVMST-UHFFFAOYSA-N 2-nitrophenanthrene-9,10-dione Chemical compound C1=CC=C2C3=CC=C([N+](=O)[O-])C=C3C(=O)C(=O)C2=C1 KNAXWOBOCVVMST-UHFFFAOYSA-N 0.000 description 1
- DSBZMUUPEHHYCY-UHFFFAOYSA-N 2-oxo-1,3,2-dioxathietan-4-one Chemical compound O=C1OS(=O)O1 DSBZMUUPEHHYCY-UHFFFAOYSA-N 0.000 description 1
- XDZQGNVQKOKOHF-UHFFFAOYSA-N 3-methyl-1h-pyrazole-4,5-dione Chemical compound CC1=NNC(=O)C1=O XDZQGNVQKOKOHF-UHFFFAOYSA-N 0.000 description 1
- JIQJZNXTUPSVCA-UHFFFAOYSA-N 3-octyl-7-thiabicyclo[4.1.0]hepta-2,4-dien-6-ol Chemical class C1=CC(CCCCCCCC)=CC2SC21O JIQJZNXTUPSVCA-UHFFFAOYSA-N 0.000 description 1
- QCTZEHIRXZGGSD-UHFFFAOYSA-N 5,7-dibromo-1h-indole-2,3-dione Chemical compound BrC1=CC(Br)=CC2=C1NC(=O)C2=O QCTZEHIRXZGGSD-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- LPGDEHBASRKTDG-UHFFFAOYSA-N N-acetylisatin Chemical compound C1=CC=C2N(C(=O)C)C(=O)C(=O)C2=C1 LPGDEHBASRKTDG-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 150000001845 chromium compounds Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- NQNHRHWFZHFAAH-XSWVPMOFSA-N etheroleic acid Chemical compound CCCC\C=C\O\C=C\C=C/CCCCCCCC(O)=O NQNHRHWFZHFAAH-XSWVPMOFSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- BQHTWZRFOSRCCH-UHFFFAOYSA-L nickel(2+);dicarbamodithioate Chemical class [Ni+2].NC([S-])=S.NC([S-])=S BQHTWZRFOSRCCH-UHFFFAOYSA-L 0.000 description 1
- BOWVQLFMWHZBEF-KTKRTIGZSA-N oleoyl ethanolamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)NCCO BOWVQLFMWHZBEF-KTKRTIGZSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- MDNAGNNHVHHNDQ-UHFFFAOYSA-M potassium;n-oxosulfamate Chemical compound [K+].[O-]S(=O)(=O)N=O MDNAGNNHVHHNDQ-UHFFFAOYSA-M 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- IVRLZJDPKUSDCF-UHFFFAOYSA-N pyrazin-2-ylhydrazine Chemical compound NNC1=CN=CC=N1 IVRLZJDPKUSDCF-UHFFFAOYSA-N 0.000 description 1
- YTRGNBTVTHPFJM-UHFFFAOYSA-N pyridazin-3-ylhydrazine Chemical compound NNC1=CC=CN=N1 YTRGNBTVTHPFJM-UHFFFAOYSA-N 0.000 description 1
- NWELCUKYUCBVKK-UHFFFAOYSA-N pyridin-2-ylhydrazine Chemical compound NNC1=CC=CC=N1 NWELCUKYUCBVKK-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- SGMABXRSPZLOPP-UHFFFAOYSA-N quinazolin-2-ylhydrazine Chemical compound C1=CC=CC2=NC(NN)=NC=C21 SGMABXRSPZLOPP-UHFFFAOYSA-N 0.000 description 1
- QMVCLSHKMIGEFN-UHFFFAOYSA-N quinolin-2-ylhydrazine Chemical compound C1=CC=CC2=NC(NN)=CC=C21 QMVCLSHKMIGEFN-UHFFFAOYSA-N 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B26/00—Hydrazone dyes; Triazene dyes
- C09B26/02—Hydrazone dyes
-
- 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
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/79—Polyolefins
- D06P3/799—Polyolefins preparing azo dyes on the material
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF0047359 | 1965-10-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1469738A1 true DE1469738A1 (de) | 1969-01-30 |
Family
ID=7101581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19651469738 Pending DE1469738A1 (de) | 1965-10-06 | 1965-10-06 | Verfahren zum Faerben und Bedrucken von Polyolefinmaterialien |
Country Status (4)
| Country | Link |
|---|---|
| BE (1) | BE687848A (forum.php) |
| DE (1) | DE1469738A1 (forum.php) |
| FR (1) | FR1496000A (forum.php) |
| GB (1) | GB1132725A (forum.php) |
-
1965
- 1965-10-06 DE DE19651469738 patent/DE1469738A1/de active Pending
-
1966
- 1966-10-05 BE BE687848D patent/BE687848A/xx unknown
- 1966-10-06 FR FR79061A patent/FR1496000A/fr not_active Expired
- 1966-10-06 GB GB44693/66A patent/GB1132725A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| GB1132725A (en) | 1968-11-06 |
| BE687848A (forum.php) | 1967-03-16 |
| FR1496000A (fr) | 1967-09-22 |
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