AU2005298779B2 - Compositions of fluorescent whitening agents - Google Patents
Compositions of fluorescent whitening agents Download PDFInfo
- Publication number
- AU2005298779B2 AU2005298779B2 AU2005298779A AU2005298779A AU2005298779B2 AU 2005298779 B2 AU2005298779 B2 AU 2005298779B2 AU 2005298779 A AU2005298779 A AU 2005298779A AU 2005298779 A AU2005298779 A AU 2005298779A AU 2005298779 B2 AU2005298779 B2 AU 2005298779B2
- Authority
- AU
- Australia
- Prior art keywords
- weight
- alkyl
- composition according
- fluorescent whitening
- acid
- 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.)
- Ceased
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- 239000000203 mixture Substances 0.000 title claims abstract description 64
- 239000006081 fluorescent whitening agent Substances 0.000 title claims abstract description 35
- 229920000642 polymer Polymers 0.000 claims abstract description 29
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- 239000000178 monomer Substances 0.000 claims abstract description 14
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- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 13
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- -1 morpholino, piperidino Chemical group 0.000 claims description 13
- 150000001413 amino acids Chemical class 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
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- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 235000004279 alanine Nutrition 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 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 description 1
- 239000003139 biocide Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229940043430 calcium compound Drugs 0.000 description 1
- 150000001674 calcium compounds Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 229960000415 diiodotyrosine Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
- AGPKZVBTJJNPAG-UHFFFAOYSA-N isoleucine Natural products CCC(C)C(N)C(O)=O AGPKZVBTJJNPAG-UHFFFAOYSA-N 0.000 description 1
- 229960000310 isoleucine Drugs 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- WFKDPJRCBCBQNT-UHFFFAOYSA-N n,2-dimethylprop-2-enamide Chemical group CNC(=O)C(C)=C WFKDPJRCBCBQNT-UHFFFAOYSA-N 0.000 description 1
- XUQIDBSIIKXTTI-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)prop-2-enamide Chemical compound OCCN(CCO)C(=O)C=C XUQIDBSIIKXTTI-UHFFFAOYSA-N 0.000 description 1
- JMCVCHBBHPFWBF-UHFFFAOYSA-N n,n-diethyl-2-methylprop-2-enamide Chemical compound CCN(CC)C(=O)C(C)=C JMCVCHBBHPFWBF-UHFFFAOYSA-N 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- 125000006606 n-butoxy group Chemical group 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- ZIWDVJPPVMGJGR-UHFFFAOYSA-N n-ethyl-2-methylprop-2-enamide Chemical compound CCNC(=O)C(C)=C ZIWDVJPPVMGJGR-UHFFFAOYSA-N 0.000 description 1
- SWPMNMYLORDLJE-UHFFFAOYSA-N n-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 description 1
- YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical group CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- 239000001254 oxidized starch Substances 0.000 description 1
- 235000013808 oxidized starch Nutrition 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 235000008729 phenylalanine Nutrition 0.000 description 1
- 230000000485 pigmenting effect Effects 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229940093430 polyethylene glycol 1500 Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000004400 serine Nutrition 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 239000004296 sodium metabisulphite Substances 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- UPDATVKGFTVGQJ-UHFFFAOYSA-N sodium;azane Chemical compound N.[Na+] UPDATVKGFTVGQJ-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 235000002374 tyrosine Nutrition 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Classifications
-
- 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
- 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
- D21H17/34—Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D21H17/37—Polymers of unsaturated acids or derivatives thereof, e.g. polyacrylates
-
- 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
- D21H17/53—Polyethers; Polyesters
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Detergent Compositions (AREA)
- Joining Of Glass To Other Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04105343 | 2004-10-27 | ||
| EP04105343.0 | 2004-10-27 | ||
| PCT/EP2005/055301 WO2006045714A1 (en) | 2004-10-27 | 2005-10-17 | Compositions of fluorescent whitening agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2005298779A1 AU2005298779A1 (en) | 2006-05-04 |
| AU2005298779B2 true AU2005298779B2 (en) | 2010-06-17 |
Family
ID=34929769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2005298779A Ceased AU2005298779B2 (en) | 2004-10-27 | 2005-10-17 | Compositions of fluorescent whitening agents |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7731820B2 (https=) |
| EP (1) | EP1805361B1 (https=) |
| JP (1) | JP2008518068A (https=) |
| KR (1) | KR20070085440A (https=) |
| CN (1) | CN101048551B (https=) |
| AT (1) | ATE441000T1 (https=) |
| AU (1) | AU2005298779B2 (https=) |
| BR (1) | BRPI0516966A (https=) |
| DE (1) | DE602005016291D1 (https=) |
| ES (1) | ES2329699T3 (https=) |
| PL (1) | PL1805361T3 (https=) |
| PT (1) | PT1805361E (https=) |
| RU (1) | RU2418904C2 (https=) |
| WO (1) | WO2006045714A1 (https=) |
| ZA (1) | ZA200702771B (https=) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101487217B1 (ko) * | 2006-05-23 | 2015-01-28 | 시바 홀딩 인크 | 직물 섬유 재료용 세제 조성물 |
| SE530020C2 (sv) * | 2006-06-15 | 2008-02-12 | Holmen Ab | Förfarande för stabilisering av vitheten hos i ytbehandlingslim/smet för papper ingående fluroescerande vitmedel (FWA) och hos av detta/dessa formade ytbehandlingsskikt |
| FR2911884B1 (fr) * | 2007-01-31 | 2010-02-26 | Arjowiggins Licensing Sas | Feuille couchee blanche imprimable par offset et ayant un haut pouvoir de fluorescence et son procede de fabrication |
| US8425723B2 (en) | 2007-04-05 | 2013-04-23 | Akzo Nobel N.V. | Process for improving optical properties of paper |
| US8227808B2 (en) * | 2007-12-06 | 2012-07-24 | Chimei Innolux Corporation | Method for manufacturing thin film transistor (TFT) and OLED display having TFTS manufactured by the same |
| CN102471603B (zh) * | 2009-07-24 | 2014-01-08 | 科莱恩金融(Bvi)有限公司 | 在施胶压榨施涂中用于遮蔽的酸性染料水溶液 |
| ES2394545T3 (es) * | 2009-09-17 | 2013-02-01 | Blankophor Gmbh & Co. Kg | Agente blanqueador fluorescente de tipo disulfo |
| BR112012031895A2 (pt) * | 2010-06-14 | 2016-11-08 | Basf Se | processo para produzir as partículas poliméricas absorvedoras de água, partículas poliméricas absorvedoras de água, e, artigo de higiene |
| AR082329A1 (es) * | 2010-07-23 | 2012-11-28 | Clariant Int Ltd | Metodo para preparar papel blanco |
| EP2412870B1 (en) * | 2010-07-30 | 2013-04-17 | Blankophor GmbH & Co. KG | Composition and process for whitening paper |
| PT2431519E (pt) * | 2010-09-17 | 2013-10-28 | Blankophor Gmbh & Co Kg | Composições de agente de branqueamento fluorescente |
| UA110221C2 (uk) * | 2010-09-28 | 2015-12-10 | Tetra Laval Holdings & Finance | Спосіб одержання пакувального матеріалу для упаковки, що стерилізується, пакувальний матеріал та упаковка |
| FR2966467B1 (fr) * | 2010-10-26 | 2014-11-07 | Berkem Sa | Composition pour le traitement du bois |
| ES2583481T3 (es) * | 2013-04-29 | 2016-09-21 | Blankophor Gmbh & Co. Kg | Uso de celulosa micronizada y agente de blanqueamiento fluorescente para el tratamiento de superficie de materiales celulósicos |
| US9181656B2 (en) * | 2013-11-06 | 2015-11-10 | Meng Jun Li | FWA formulation used for the papermaking process |
| CN110717446B (zh) | 2014-03-13 | 2023-11-07 | 日本电气株式会社 | 检测设备、检测方法和记录介质 |
| CN106087384A (zh) * | 2016-06-21 | 2016-11-09 | 太仓市东明化工有限公司 | 一种织物用耐水型荧光增白剂 |
| CN107602492A (zh) * | 2017-10-12 | 2018-01-19 | 贺州学院 | 一种两性丙烯酸酯季铵盐荧光增白剂的合成与应用 |
| PL3623392T3 (pl) * | 2018-09-14 | 2024-01-15 | Archroma Ip Gmbh | Optycznie rozjaśnione lateksy |
| AU2019362820B2 (en) * | 2018-10-17 | 2025-07-24 | Basf Se | Additives to stabilize polyacrylamide co-polymer solutions under high shear conditions |
| WO2020251532A1 (en) * | 2019-06-10 | 2020-12-17 | Hewlett-Packard Development Company, L.P. | Three-dimensional printing |
| CN116296703B (zh) * | 2023-05-17 | 2023-07-28 | 广州盛安医学检验有限公司 | 一种荧光染色液在制备阴道炎检测试剂中的应用 |
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| US4670183A (en) * | 1983-11-15 | 1987-06-02 | The Dow Chemical Company | Method and compositions relating to the activation of fluorescent whitening agents |
| WO2003021041A2 (de) * | 2001-09-03 | 2003-03-13 | Basf Aktiengesellschaft | Verfahren zur erhöhung der weisse von papier mit hilfe von kationischen polyelektrolyten |
| WO2003052205A1 (de) * | 2001-12-17 | 2003-06-26 | Basf Aktiengesellschaft | Verfahren zur herstellung von papier, pappe und karton |
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| DE2928052A1 (de) * | 1978-07-17 | 1980-01-31 | Ciba Geigy Ag | Stabile stilbenaufhellerloesungen |
| JPS5725365A (en) * | 1980-07-22 | 1982-02-10 | Showa Kagaku Kogyo Kk | Dyestuff salt-containing fluorescent brightener composition |
| JPS608371A (ja) * | 1983-06-27 | 1985-01-17 | Sumitomo Chem Co Ltd | 螢光増白剤水性組成物 |
| JPS6131468A (ja) * | 1984-07-23 | 1986-02-13 | Nippon Kayaku Co Ltd | 水性液状螢光増白染料組成物 |
| DE3502038A1 (de) * | 1985-01-23 | 1986-07-24 | Sandoz-Patent-GmbH, 7850 Lörrach | Waessrige aufhellerpraeparate und deren verwendung im papierstrich |
| GB9422280D0 (en) * | 1994-11-04 | 1994-12-21 | Ciba Geigy Ag | Fluorescent whitening agent formulation |
| GB2294708B (en) * | 1994-11-04 | 1998-08-05 | Ciba Geigy Ag | Fluorescent whitening agent formulation |
| DE69920409T2 (de) * | 1998-02-20 | 2005-10-06 | Ciba Speciality Chemicals Holding Inc. | Verfahren zur herstellung von stilbenverbindungen |
| US6202294B1 (en) * | 1998-09-25 | 2001-03-20 | Lucent Technologies Inc. | EMI/RFI shield assembly cover removal tool |
| JP4340995B2 (ja) * | 1999-07-09 | 2009-10-07 | 星光Ｐｍｃ株式会社 | 紙塗工用組成物、並びにそれを塗工したクリアコート紙及びピグメントコート紙 |
| GB9917508D0 (en) | 1999-07-27 | 1999-09-29 | Ciba Spec Chem Water Treat Ltd | Coating colour |
| EP1200675A1 (en) * | 1999-08-05 | 2002-05-02 | Ciba SC Holding AG | Use of whitening pigments for whitening paper coating compositions |
| WO2001012900A1 (en) | 1999-08-13 | 2001-02-22 | Ciba Specialty Chemicals Holding Inc. | Formulations of fluorescent whitening agents |
| AU6842600A (en) * | 1999-09-10 | 2001-04-17 | Ciba Specialty Chemicals Holding Inc. | Triazinylaminostilbene derivative as fluorescent whitening agents |
| DE10055592A1 (de) * | 2000-11-09 | 2002-05-23 | Basf Ag | Papierstreichmassen |
| GB0100610D0 (en) * | 2001-01-10 | 2001-02-21 | Clariant Int Ltd | Improvements in or relating to organic compounds |
| WO2003020808A1 (de) * | 2001-09-03 | 2003-03-13 | Basf Aktiengesellschaft | Verstärkung der wirkung von optischen aufhellern mit hilfe von polymeren |
| GB0125177D0 (en) * | 2001-10-19 | 2001-12-12 | Clariant Int Ltd | Improvements in or relating to organic compounds |
| DE10217677A1 (de) * | 2002-04-19 | 2003-11-06 | Bayer Ag | Verwendung von Aufhellern zur Herstellung von Streichmassen |
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-
2005
- 2005-10-17 BR BRPI0516966-6A patent/BRPI0516966A/pt not_active IP Right Cessation
- 2005-10-17 PL PL05796932T patent/PL1805361T3/pl unknown
- 2005-10-17 CN CN2005800364454A patent/CN101048551B/zh not_active Expired - Fee Related
- 2005-10-17 JP JP2007538385A patent/JP2008518068A/ja active Pending
- 2005-10-17 PT PT05796932T patent/PT1805361E/pt unknown
- 2005-10-17 DE DE602005016291T patent/DE602005016291D1/de not_active Expired - Lifetime
- 2005-10-17 WO PCT/EP2005/055301 patent/WO2006045714A1/en not_active Ceased
- 2005-10-17 ES ES05796932T patent/ES2329699T3/es not_active Expired - Lifetime
- 2005-10-17 KR KR1020077011774A patent/KR20070085440A/ko not_active Ceased
- 2005-10-17 AT AT05796932T patent/ATE441000T1/de active
- 2005-10-17 AU AU2005298779A patent/AU2005298779B2/en not_active Ceased
- 2005-10-17 EP EP05796932A patent/EP1805361B1/en not_active Expired - Lifetime
- 2005-10-17 US US11/665,886 patent/US7731820B2/en not_active Expired - Fee Related
- 2005-10-17 RU RU2007119642/02A patent/RU2418904C2/ru not_active IP Right Cessation
-
2007
- 2007-04-03 ZA ZA200702771A patent/ZA200702771B/xx unknown
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4670183A (en) * | 1983-11-15 | 1987-06-02 | The Dow Chemical Company | Method and compositions relating to the activation of fluorescent whitening agents |
| WO2003021041A2 (de) * | 2001-09-03 | 2003-03-13 | Basf Aktiengesellschaft | Verfahren zur erhöhung der weisse von papier mit hilfe von kationischen polyelektrolyten |
| US20040182533A1 (en) * | 2001-09-03 | 2004-09-23 | Thierry Blum | Method for increasing the whiteness of paper by means of cationic polyelectrolytes |
| WO2003052205A1 (de) * | 2001-12-17 | 2003-06-26 | Basf Aktiengesellschaft | Verfahren zur herstellung von papier, pappe und karton |
Also Published As
| Publication number | Publication date |
|---|---|
| CN101048551A (zh) | 2007-10-03 |
| AU2005298779A1 (en) | 2006-05-04 |
| ES2329699T3 (es) | 2009-11-30 |
| US20080073617A1 (en) | 2008-03-27 |
| ATE441000T1 (de) | 2009-09-15 |
| RU2007119642A (ru) | 2008-12-10 |
| BRPI0516966A (pt) | 2008-09-30 |
| CN101048551B (zh) | 2012-02-15 |
| RU2418904C2 (ru) | 2011-05-20 |
| EP1805361B1 (en) | 2009-08-26 |
| WO2006045714A1 (en) | 2006-05-04 |
| EP1805361A1 (en) | 2007-07-11 |
| US7731820B2 (en) | 2010-06-08 |
| PL1805361T3 (pl) | 2010-01-29 |
| KR20070085440A (ko) | 2007-08-27 |
| PT1805361E (pt) | 2009-10-06 |
| ZA200702771B (en) | 2008-08-27 |
| DE602005016291D1 (de) | 2009-10-08 |
| JP2008518068A (ja) | 2008-05-29 |
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