RU2004139044A - Отбеливающие пигменты - Google Patents
Отбеливающие пигменты Download PDFInfo
- Publication number
- RU2004139044A RU2004139044A RU2004139044/04A RU2004139044A RU2004139044A RU 2004139044 A RU2004139044 A RU 2004139044A RU 2004139044/04 A RU2004139044/04 A RU 2004139044/04A RU 2004139044 A RU2004139044 A RU 2004139044A RU 2004139044 A RU2004139044 A RU 2004139044A
- Authority
- RU
- Russia
- Prior art keywords
- sub
- alkyl
- acid
- hydroxyalkyl
- nhc
- Prior art date
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- 239000000049 pigment Substances 0.000 title claims abstract 16
- 230000002087 whitening effect Effects 0.000 title claims abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract 7
- 239000000203 mixture Substances 0.000 claims abstract 7
- -1 morpholino, piperidino, pyrrolidino Chemical group 0.000 claims abstract 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 claims abstract 4
- 229920000877 Melamine resin Polymers 0.000 claims abstract 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims abstract 4
- 150000001413 amino acids Chemical class 0.000 claims abstract 4
- 125000003277 amino group Chemical group 0.000 claims abstract 4
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims abstract 4
- 238000000034 method Methods 0.000 claims abstract 4
- 238000006068 polycondensation reaction Methods 0.000 claims abstract 4
- 239000011591 potassium Chemical group 0.000 claims abstract 4
- 229910052700 potassium Inorganic materials 0.000 claims abstract 4
- 239000000047 product Substances 0.000 claims abstract 4
- 229910052708 sodium Inorganic materials 0.000 claims abstract 4
- 239000011734 sodium Chemical group 0.000 claims abstract 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims abstract 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical group [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract 3
- 239000011575 calcium Chemical group 0.000 claims abstract 3
- 229910052791 calcium Inorganic materials 0.000 claims abstract 3
- 239000011248 coating agent Substances 0.000 claims abstract 3
- 238000000576 coating method Methods 0.000 claims abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 3
- 239000001257 hydrogen Substances 0.000 claims abstract 3
- 229910052749 magnesium Inorganic materials 0.000 claims abstract 3
- 239000007795 chemical reaction product Substances 0.000 claims abstract 2
- 239000011777 magnesium Chemical group 0.000 claims abstract 2
- 239000013042 solid detergent Substances 0.000 claims abstract 2
- 230000037072 sun protection Effects 0.000 claims abstract 2
- 239000004753 textile Substances 0.000 claims abstract 2
- 238000004061 bleaching Methods 0.000 claims 12
- 150000001875 compounds Chemical class 0.000 claims 8
- 239000002253 acid Substances 0.000 claims 4
- 235000001014 amino acid Nutrition 0.000 claims 3
- 229940024606 amino acid Drugs 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 claims 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 claims 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 claims 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 2
- 125000000539 amino acid group Chemical group 0.000 claims 2
- 239000011230 binding agent Substances 0.000 claims 2
- HANVTCGOAROXMV-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.NC1=NC(N)=NC(N)=N1 HANVTCGOAROXMV-UHFFFAOYSA-N 0.000 claims 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 claims 2
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 claims 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 claims 1
- MYFWUKZYURBPHI-BYPYZUCNSA-N (2s)-2-amino-3-(1h-imidazol-2-yl)propanoic acid Chemical compound OC(=O)[C@@H](N)CC1=NC=CN1 MYFWUKZYURBPHI-BYPYZUCNSA-N 0.000 claims 1
- KYNMONSTYCGIDJ-VIFPVBQESA-N (2s)-2-amino-3-(1h-indol-2-yl)propanoic acid Chemical compound C1=CC=C2NC(C[C@H](N)C(O)=O)=CC2=C1 KYNMONSTYCGIDJ-VIFPVBQESA-N 0.000 claims 1
- NYPYHUZRZVSYKL-UHFFFAOYSA-N -3,5-Diiodotyrosine Natural products OC(=O)C(N)CC1=CC(I)=C(O)C(I)=C1 NYPYHUZRZVSYKL-UHFFFAOYSA-N 0.000 claims 1
- QWCKQJZIFLGMSD-UHFFFAOYSA-N 2-Aminobutanoic acid Natural products CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 claims 1
- XDDMZVMWZMSAMX-FHAQVOQBSA-N 2-amino-3-methylpentanoic acid;(2s,3s)-2-amino-3-methylpentanoic acid Chemical compound CCC(C)C(N)C(O)=O.CC[C@H](C)[C@H](N)C(O)=O XDDMZVMWZMSAMX-FHAQVOQBSA-N 0.000 claims 1
- NYPYHUZRZVSYKL-ZETCQYMHSA-N 3,5-diiodo-L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC(I)=C(O)C(I)=C1 NYPYHUZRZVSYKL-ZETCQYMHSA-N 0.000 claims 1
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 claims 1
- REJHVSOVQBJEBF-UHFFFAOYSA-N 5-azaniumyl-2-[2-(4-azaniumyl-2-sulfonatophenyl)ethenyl]benzenesulfonate Chemical compound OS(=O)(=O)C1=CC(N)=CC=C1C=CC1=CC=C(N)C=C1S(O)(=O)=O REJHVSOVQBJEBF-UHFFFAOYSA-N 0.000 claims 1
- 239000004475 Arginine Substances 0.000 claims 1
- QWCKQJZIFLGMSD-GSVOUGTGSA-N D-alpha-aminobutyric acid Chemical compound CC[C@@H](N)C(O)=O QWCKQJZIFLGMSD-GSVOUGTGSA-N 0.000 claims 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 claims 1
- 239000004471 Glycine Substances 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- NNIVFXCKHNRSRL-VKHMYHEASA-N Hydroxyglutamic acid Chemical compound ON[C@H](C(O)=O)CCC(O)=O NNIVFXCKHNRSRL-VKHMYHEASA-N 0.000 claims 1
- SNDPXSYFESPGGJ-BYPYZUCNSA-N L-2-aminopentanoic acid Chemical compound CCC[C@H](N)C(O)=O SNDPXSYFESPGGJ-BYPYZUCNSA-N 0.000 claims 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 claims 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 claims 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 claims 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 claims 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 claims 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 claims 1
- SNDPXSYFESPGGJ-UHFFFAOYSA-N L-norVal-OH Natural products CCCC(N)C(O)=O SNDPXSYFESPGGJ-UHFFFAOYSA-N 0.000 claims 1
- LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 claims 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 claims 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 claims 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 claims 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 claims 1
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 claims 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 claims 1
- 108010077895 Sarcosine Proteins 0.000 claims 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 claims 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 claims 1
- 239000004473 Threonine Substances 0.000 claims 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 claims 1
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 claims 1
- 235000004279 alanine Nutrition 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 claims 1
- 235000003704 aspartic acid Nutrition 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 claims 1
- 239000007844 bleaching agent Substances 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000008199 coating composition Substances 0.000 claims 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 claims 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 claims 1
- 235000018417 cysteine Nutrition 0.000 claims 1
- 229960000415 diiodotyrosine Drugs 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 235000013922 glutamic acid Nutrition 0.000 claims 1
- 239000004220 glutamic acid Substances 0.000 claims 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 claims 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 239000001023 inorganic pigment Substances 0.000 claims 1
- 229930182817 methionine Natural products 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 229960003104 ornithine Drugs 0.000 claims 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 claims 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229940043230 sarcosine Drugs 0.000 claims 1
- 229960003080 taurine Drugs 0.000 claims 1
- 239000002562 thickening agent Substances 0.000 claims 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 claims 1
- 239000004474 valine Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 3
- 238000002360 preparation method Methods 0.000 abstract 3
- 239000006081 fluorescent whitening agent Substances 0.000 abstract 2
- JZLWSRCQCPAUDP-UHFFFAOYSA-N 1,3,5-triazine-2,4,6-triamine;urea Chemical compound NC(N)=O.NC1=NC(N)=NC(N)=N1 JZLWSRCQCPAUDP-UHFFFAOYSA-N 0.000 abstract 1
- 125000005210 alkyl ammonium group Chemical group 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 0 C1NCN*1 Chemical compound C1NCN*1 0.000 description 2
- HCXJYPBBVSRTQP-NSHDSACASA-N CCCCC[C@H](C)CCCNC Chemical compound CCCCC[C@H](C)CCCNC HCXJYPBBVSRTQP-NSHDSACASA-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
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
-
- 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
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/14—Styryl dyes
-
- 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
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0072—Preparations with anionic dyes or reactive dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
- D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
- D06L4/60—Optical bleaching or brightening
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
- D06M13/355—Heterocyclic compounds having six-membered heterocyclic rings
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/20—Macromolecular organic compounds
- D21H17/33—Synthetic macromolecular compounds
- D21H17/46—Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/47—Condensation polymers of aldehydes or ketones
- D21H17/49—Condensation polymers of aldehydes or ketones with compounds containing hydrogen bound to nitrogen
- D21H17/51—Triazines, e.g. melamine
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/30—Luminescent or fluorescent substances, e.g. for optical bleaching
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H19/00—Coated paper; Coating material
- D21H19/36—Coatings with pigments
- D21H19/38—Coatings with pigments characterised by the pigments
- D21H19/42—Coatings with pigments characterised by the pigments at least partly organic
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Detergent Compositions (AREA)
- Paper (AREA)
- Paints Or Removers (AREA)
- Cosmetics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02405474.4 | 2002-06-11 | ||
| EP02405474 | 2002-06-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2004139044A true RU2004139044A (ru) | 2006-01-10 |
Family
ID=29724598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2004139044/04A RU2004139044A (ru) | 2002-06-11 | 2003-06-03 | Отбеливающие пигменты |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US20050203221A1 (https=) |
| EP (1) | EP1511901B1 (https=) |
| JP (1) | JP2005529217A (https=) |
| KR (1) | KR20050012787A (https=) |
| CN (1) | CN1659339A (https=) |
| AT (1) | ATE366337T1 (https=) |
| AU (1) | AU2003238207A1 (https=) |
| BR (1) | BR0311712A (https=) |
| CA (1) | CA2486589A1 (https=) |
| DE (1) | DE60314746T2 (https=) |
| ES (1) | ES2290473T3 (https=) |
| IL (1) | IL165025A0 (https=) |
| MX (1) | MXPA04011842A (https=) |
| RU (1) | RU2004139044A (https=) |
| WO (1) | WO2003104560A1 (https=) |
| ZA (1) | ZA200408888B (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2495972C2 (ru) * | 2008-03-26 | 2013-10-20 | Клариант Финанс (Бви) Лимитед | Усовершенствованные композиции для оптического отбеливания |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005090545A1 (en) * | 2004-03-12 | 2005-09-29 | Ciba Specialty Chemicals Holding Inc. | Process for the preparation of brightener pigments |
| WO2006015963A1 (en) * | 2004-08-12 | 2006-02-16 | Ciba Specialty Chemicals Holding Inc. | Fluorescent pigments for coating compositions |
| US20080202716A1 (en) * | 2004-10-20 | 2008-08-28 | Goetz Scheffler | Amphoteric 4-4'-Bis (Triazinylamino) Stilbene-2,2'-Disulfonic Acid Derivatives as Optical Brighteners for Paper |
| BRPI0516966A (pt) * | 2004-10-27 | 2008-09-30 | Ciba Sc Holding Ag | composições de agentes de branqueamento fluorescente |
| US7732382B2 (en) * | 2006-02-14 | 2010-06-08 | E.I. Du Pont De Nemours And Company | Cross-linking composition and method of use |
| ES2394545T3 (es) * | 2009-09-17 | 2013-02-01 | Blankophor Gmbh & Co. Kg | Agente blanqueador fluorescente de tipo disulfo |
| EP3020768B1 (en) | 2010-05-18 | 2018-04-25 | Milliken & Company | Optical brighteners and compositions comprising the same |
| CN102906239B (zh) | 2010-05-18 | 2015-09-09 | 美利肯公司 | 荧光增白剂及含有其的组合物 |
| CN103183966B (zh) * | 2011-12-27 | 2014-06-04 | 上海雅运纺织助剂有限公司 | 水溶性良好的二磺酸荧光增白剂及其制备方法 |
| PT2781648E (pt) * | 2013-03-21 | 2016-03-07 | Clariant Int Ltd | Agentes de branqueamento ótico para impressão a jato de tinta de alta qualidade |
| CN104312196B (zh) * | 2014-09-05 | 2016-02-10 | 旭泰（太仓）精细化工有限公司 | 一种四磺酸液体荧光增白剂及其合成方法与应用 |
| CN109082139B (zh) * | 2018-07-04 | 2021-04-23 | 丽王化工(南通)有限公司 | 一种用于油相体系的荧光颜料粉末及其制备方法 |
| PL3623392T3 (pl) * | 2018-09-14 | 2024-01-15 | Archroma Ip Gmbh | Optycznie rozjaśnione lateksy |
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| US2851424A (en) * | 1957-06-28 | 1958-09-09 | Switzer Brothers Inc | Fluorescent compositions |
| US3327018A (en) * | 1963-03-01 | 1967-06-20 | Dal Mon Research Co | Fluorescent aldehyde-triazinyl stilbino condensation products |
| CH529770A (de) * | 1969-12-11 | 1972-10-31 | Sandoz Ag | Verfahren zur Herstellung neuer Stilbenverbindungen |
| GB1391593A (en) * | 1971-06-17 | 1975-04-23 | Ici Ltd | Coating compositions |
| CH617453A5 (en) * | 1976-03-10 | 1980-05-30 | Ciba Geigy Ag | Stable, commercial aqueous solutions of water-soluble brighteners |
| DE3112435A1 (de) * | 1981-03-28 | 1982-10-07 | Bayer Ag, 5090 Leverkusen | Waessrige aminoplastdispersionen |
| JPS5949537A (ja) * | 1982-09-14 | 1984-03-22 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料の処理方法 |
| GB2284829A (en) * | 1993-12-15 | 1995-06-21 | Ciba Geigy Ag | Filler and coating composition for paper |
| ATE244227T1 (de) * | 1997-03-25 | 2003-07-15 | Ciba Sc Holding Ag | 4,4'-diaminostilben-2,2'-disulfonsäurederivate |
| EP0905317B1 (en) * | 1997-09-16 | 2009-12-23 | Basf Se | A method for optically brightening paper |
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| DE69920409T2 (de) * | 1998-02-20 | 2005-10-06 | Ciba Speciality Chemicals Holding Inc. | Verfahren zur herstellung von stilbenverbindungen |
| DE19920784A1 (de) * | 1999-05-05 | 2000-11-09 | Bayer Ag | Stilbenaufheller |
| EP1200675A1 (en) * | 1999-08-05 | 2002-05-02 | Ciba SC Holding AG | Use of whitening pigments for whitening paper coating compositions |
| GB0125177D0 (en) * | 2001-10-19 | 2001-12-12 | Clariant Int Ltd | Improvements in or relating to organic compounds |
-
2003
- 2003-06-03 BR BR0311712-0A patent/BR0311712A/pt not_active Application Discontinuation
- 2003-06-03 AT AT03735531T patent/ATE366337T1/de not_active IP Right Cessation
- 2003-06-03 ES ES03735531T patent/ES2290473T3/es not_active Expired - Lifetime
- 2003-06-03 DE DE60314746T patent/DE60314746T2/de not_active Expired - Fee Related
- 2003-06-03 MX MXPA04011842A patent/MXPA04011842A/es active IP Right Grant
- 2003-06-03 KR KR10-2004-7020139A patent/KR20050012787A/ko not_active Withdrawn
- 2003-06-03 CA CA002486589A patent/CA2486589A1/en not_active Abandoned
- 2003-06-03 WO PCT/EP2003/005803 patent/WO2003104560A1/en not_active Ceased
- 2003-06-03 AU AU2003238207A patent/AU2003238207A1/en not_active Abandoned
- 2003-06-03 US US10/515,898 patent/US20050203221A1/en not_active Abandoned
- 2003-06-03 EP EP03735531A patent/EP1511901B1/en not_active Expired - Lifetime
- 2003-06-03 RU RU2004139044/04A patent/RU2004139044A/ru not_active Application Discontinuation
- 2003-06-03 JP JP2004511612A patent/JP2005529217A/ja active Pending
- 2003-06-03 CN CN03813456XA patent/CN1659339A/zh active Pending
-
2004
- 2004-11-03 ZA ZA200408888A patent/ZA200408888B/en unknown
- 2004-11-04 IL IL16502504A patent/IL165025A0/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2495972C2 (ru) * | 2008-03-26 | 2013-10-20 | Клариант Финанс (Бви) Лимитед | Усовершенствованные композиции для оптического отбеливания |
| RU2495973C2 (ru) * | 2008-03-26 | 2013-10-20 | Клариант Финанс (Бви) Лимитед | Усовершенствованные композиции для оптического отбеливания |
Also Published As
| Publication number | Publication date |
|---|---|
| BR0311712A (pt) | 2005-03-15 |
| US20050203221A1 (en) | 2005-09-15 |
| MXPA04011842A (es) | 2005-03-31 |
| EP1511901A1 (en) | 2005-03-09 |
| IL165025A0 (en) | 2005-12-18 |
| CN1659339A (zh) | 2005-08-24 |
| ES2290473T3 (es) | 2008-02-16 |
| CA2486589A1 (en) | 2003-12-18 |
| DE60314746D1 (de) | 2007-08-16 |
| WO2003104560A1 (en) | 2003-12-18 |
| ZA200408888B (en) | 2005-11-30 |
| JP2005529217A (ja) | 2005-09-29 |
| EP1511901B1 (en) | 2007-07-04 |
| ATE366337T1 (de) | 2007-07-15 |
| AU2003238207A1 (en) | 2003-12-22 |
| KR20050012787A (ko) | 2005-02-02 |
| DE60314746T2 (de) | 2008-03-06 |
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| FA93 | Acknowledgement of application withdrawn (no request for examination) |
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