ZA200606681B - Concentrated optical brightener solutions - Google Patents

Concentrated optical brightener solutions Download PDF

Info

Publication number: ZA200606681B
Authority: ZA; South Africa
Prior art keywords: optical brightener; aqueous solution; mol; formula; storage
Prior art date: 2004-03-05

Application number

ZA200606681A

Other languages

English (en)

Inventor

Jackson Andrew Clive

Original Assignee

Clariant Finance Bvi Ltd

Priority date (The priority date 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 date listed.)

2004-03-05

Filing date

2006-08-11

Publication date

2008-02-27

2006-08-11 Application filed by Clariant Finance Bvi Ltd filed Critical Clariant Finance Bvi Ltd

2008-02-27 Publication of ZA200606681B publication Critical patent/ZA200606681B/en

Links

230000003287 optical effect Effects 0.000 title claims description 22
239000000243 solution Substances 0.000 claims description 22
239000007864 aqueous solution Substances 0.000 claims description 20
239000008199 coating composition Substances 0.000 claims description 13
150000004820 halides Chemical class 0.000 claims description 11
150000001412 amines Chemical class 0.000 claims description 10
238000006243 chemical reaction Methods 0.000 claims description 10
-1 alkali metal cation Chemical class 0.000 claims description 9
239000012463 white pigment Substances 0.000 claims description 9
229910052783 alkali metal Inorganic materials 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 7
150000001340 alkali metals Chemical class 0.000 claims description 5
238000005282 brightening Methods 0.000 claims description 5
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
239000006227 byproduct Substances 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
238000005374 membrane filtration Methods 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
238000002360 preparation method Methods 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
230000002528 anti-freeze Effects 0.000 claims description 3
239000000969 carrier Substances 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
239000000758 substrate Substances 0.000 claims description 3
238000000108 ultra-filtration Methods 0.000 claims description 3
FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 claims description 2
239000008139 complexing agent Substances 0.000 claims description 2
150000004985 diamines Chemical class 0.000 claims description 2
238000003541 multi-stage reaction Methods 0.000 claims description 2
239000003755 preservative agent Substances 0.000 claims description 2
150000003839 salts Chemical class 0.000 claims description 2
101001051799 Aedes aegypti Molybdenum cofactor sulfurase 3 Proteins 0.000 claims 1
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 19
239000011230 binding agent Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
239000004202 carbamide Substances 0.000 description 5
239000000203 mixture Substances 0.000 description 5
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
239000002585 base Substances 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
238000001556 precipitation Methods 0.000 description 3
238000006467 substitution reaction Methods 0.000 description 3
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 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
229920002134 Carboxymethyl cellulose Polymers 0.000 description 2
CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 description 2
CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 2
WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000004982 aromatic amines Chemical class 0.000 description 2
229960005261 aspartic acid Drugs 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
235000010948 carboxy methyl cellulose Nutrition 0.000 description 2
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000004816 latex Substances 0.000 description 2
229920000126 latex Polymers 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920002451 polyvinyl alcohol Polymers 0.000 description 2
235000019422 polyvinyl alcohol Nutrition 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
239000008107 starch Substances 0.000 description 2
235000019698 starch Nutrition 0.000 description 2
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 2
239000000725 suspension Substances 0.000 description 2
230000002087 whitening effect Effects 0.000 description 2
HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
LDCCBULMAFILCT-UHFFFAOYSA-N 2-aminobenzene-1,4-disulfonic acid Chemical compound NC1=CC(S(O)(=O)=O)=CC=C1S(O)(=O)=O LDCCBULMAFILCT-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
229920005789 ACRONAL® acrylic binder Polymers 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound 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 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
239000002174 Styrene-butadiene Substances 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
235000011054 acetic acid Nutrition 0.000 description 1
239000000654 additive Substances 0.000 description 1
WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
229910021502 aluminium hydroxide Inorganic materials 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
235000011132 calcium sulphate Nutrition 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000005038 ethylene vinyl acetate Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
229960002989 glutamic acid Drugs 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
235000011167 hydrochloric acid Nutrition 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000002609 medium Substances 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000003263 primary aromatic amine group Chemical group 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000004513 sizing Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000011115 styrene butadiene Substances 0.000 description 1
229920003048 styrene butadiene rubber Polymers 0.000 description 1
229920001909 styrene-acrylic polymer Polymers 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Paper (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pigments, Carbon Blacks, Or Wood Stains (AREA)
Coloring (AREA)

ZA200606681A 2004-03-05 2006-08-11 Concentrated optical brightener solutions ZA200606681B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP04005210A EP1571149A1 (fr)	2004-03-05	2004-03-05	Solutions d'azurants optiques

Publications (1)

Publication Number	Publication Date
ZA200606681B true ZA200606681B (en)	2008-02-27

Family

ID=34746007

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200606681A ZA200606681B (en)	2004-03-05	2006-08-11	Concentrated optical brightener solutions

Country Status (14)

Country	Link
US (1)	US20070186358A1 (fr)
EP (2)	EP1571149A1 (fr)
JP (1)	JP2007526383A (fr)
KR (1)	KR20070008584A (fr)
CN (1)	CN1926120A (fr)
AU (1)	AU2005225623A1 (fr)
BR (1)	BRPI0508459A (fr)
CA (1)	CA2553556A1 (fr)
NO (1)	NO20063924L (fr)
PE (1)	PE20060182A1 (fr)
RU (1)	RU2380364C2 (fr)
TW (1)	TW200602534A (fr)
WO (1)	WO2005092868A1 (fr)
ZA (1)	ZA200606681B (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1712677A1 (fr) *	2005-04-08	2006-10-18	Clariant International Ltd.	Solutions aqueuses d'azurants optiques
US8758886B2 (en)	2005-10-14	2014-06-24	International Paper Company	Recording sheet with improved image dry time
BRPI0909829B1 (pt) *	2008-03-26	2018-11-21	Archroma Ip Gmbh	composições aperfeiçoadas de abrilhantamento óptico
AU2014259497B2 (en) *	2008-03-26	2016-05-12	Archroma Ip Gmbh	Improved optical brightening compositions
RU2495973C2 (ru) *	2008-03-26	2013-10-20	Клариант Финанс (Бви) Лимитед	Усовершенствованные композиции для оптического отбеливания
WO2009124075A1 (fr)	2008-03-31	2009-10-08	International Paper Company	Feuille d'enregistrement à qualité d'impression améliorée et à faible niveau d'additifs
ES2390932T5 (es) *	2008-11-27	2020-09-14	Archroma Ip Gmbh	Composiciones abrillantadoras ópticas para la impresión por chorro de tinta de alta calidad
US20100129553A1 (en) *	2008-11-27	2010-05-27	International Paper Company	Optical Brightening Compositions For High Quality Inkjet Printing
US8574690B2 (en)	2009-12-17	2013-11-05	International Paper Company	Printable substrates with improved dry time and acceptable print density by using monovalent salts
US8652593B2 (en)	2009-12-17	2014-02-18	International Paper Company	Printable substrates with improved brightness from OBAs in presence of multivalent metal salts
TWI506183B (zh) *	2010-02-11	2015-11-01	Clariant Finance Bvi Ltd	於施漿壓印應用中用於調色光之水性上漿組成物
US8608908B2 (en)	2010-04-02	2013-12-17	International Paper Company	Method and system using low fatty acid starches in paper sizing composition to inhibit deposition of multivalent fatty acid salts
US8440053B2 (en)	2010-04-02	2013-05-14	International Paper Company	Method and system using surfactants in paper sizing composition to inhibit deposition of multivalent fatty acid salts
WO2011139481A1 (fr)	2010-05-04	2011-11-10	International Paper Company	Substrats imprimés revêtus résistant aux surligneurs acides et aux solutions d'impression
CN103003492B (zh)	2010-07-23	2015-04-08	国际纸业公司	以较低油墨用量提供较高印刷质量和分辨率的涂布可印刷基底
US8697203B2 (en)	2010-11-16	2014-04-15	International Paper Company	Paper sizing composition with salt of calcium (II) and organic acid, products made thereby, method of using, and method of making
EP2781648B1 (fr) *	2013-03-21	2016-01-06	Clariant International Ltd.	Agents de blanchiment optique pour impression à jet d'encre de haute qualité
ES2959753T3 (es) *	2018-09-14	2024-02-28	Archroma Ip Gmbh	Látex ópticamente abrillantados
CN110424182A (zh) *	2019-07-08	2019-11-08	浙江金龙纸业有限公司	一种环境友好型复配表面施胶剂及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62106965A (ja) *	1985-11-05	1987-05-18	Shin Nisso Kako Co Ltd	螢光増白剤
DE69816135T2 (de) *	1997-03-25	2004-04-22	Ciba Speciality Chemicals Holding Inc.	4,4'-Diaminostilben-2,2'-disulfonsäurederivate
GB9930177D0 (en) *	1999-12-22	2000-02-09	Clariant Int Ltd	Improvements in or relating to organic compounds
GB0127903D0 (en) *	2001-11-21	2002-01-16	Clariant Int Ltd	Improvements relating to organic compounds
RU2223957C2 (ru) *	2001-11-28	2004-02-20	Открытое акционерное общество "Пигмент"	Способ получения производных 4,4'-диаминостильбен-2,2'-дисульфокислоты

2004
- 2004-03-05 EP EP04005210A patent/EP1571149A1/fr not_active Withdrawn
2005
- 2005-02-05 TW TW094104029A patent/TW200602534A/zh unknown
- 2005-02-17 RU RU2006131669/04A patent/RU2380364C2/ru active
- 2005-02-17 BR BRPI0508459-8A patent/BRPI0508459A/pt not_active IP Right Cessation
- 2005-02-17 WO PCT/IB2005/000407 patent/WO2005092868A1/fr not_active Ceased
- 2005-02-17 AU AU2005225623A patent/AU2005225623A1/en not_active Abandoned
- 2005-02-17 CA CA002553556A patent/CA2553556A1/fr not_active Abandoned
- 2005-02-17 EP EP05702518A patent/EP1735290A1/fr not_active Withdrawn
- 2005-02-17 JP JP2007501362A patent/JP2007526383A/ja active Pending
- 2005-02-17 CN CNA2005800066309A patent/CN1926120A/zh active Pending
- 2005-02-17 US US10/591,572 patent/US20070186358A1/en not_active Abandoned
- 2005-02-17 KR KR1020067017971A patent/KR20070008584A/ko not_active Ceased
- 2005-03-02 PE PE2005000240A patent/PE20060182A1/es not_active Application Discontinuation
2006
- 2006-08-11 ZA ZA200606681A patent/ZA200606681B/en unknown
- 2006-09-01 NO NO20063924A patent/NO20063924L/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
BRPI0508459A (pt)	2007-07-31
AU2005225623A1 (en)	2005-10-06
RU2380364C2 (ru)	2010-01-27
EP1571149A1 (fr)	2005-09-07
WO2005092868A1 (fr)	2005-10-06
KR20070008584A (ko)	2007-01-17
NO20063924L (no)	2006-10-05
JP2007526383A (ja)	2007-09-13
RU2006131669A (ru)	2008-03-10
US20070186358A1 (en)	2007-08-16
EP1735290A1 (fr)	2006-12-27
TW200602534A (en)	2006-01-16
CA2553556A1 (fr)	2005-10-06
PE20060182A1 (es)	2006-03-15
CN1926120A (zh)	2007-03-07

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