MXPA06007817A - Uso de compuestos complejos de metales, que comprenden ligaduras derivadas de piridina-pirimidina o s-triazina como catalizadores para oxidaciones con acidos peroxi organicos y/o precursores de acidos peroxi organicos y h2o2. - Google Patents
Uso de compuestos complejos de metales, que comprenden ligaduras derivadas de piridina-pirimidina o s-triazina como catalizadores para oxidaciones con acidos peroxi organicos y/o precursores de acidos peroxi organicos y h2o2.Info
- Publication number
- MXPA06007817A MXPA06007817A MXPA06007817A MXPA06007817A MXPA06007817A MX PA06007817 A MXPA06007817 A MX PA06007817A MX PA06007817 A MXPA06007817 A MX PA06007817A MX PA06007817 A MXPA06007817 A MX PA06007817A MX PA06007817 A MXPA06007817 A MX PA06007817A
- Authority
- MX
- Mexico
- Prior art keywords
- substituted
- unsubstituted
- phenyl
- hydroxy
- hydrogen
- Prior art date
Links
- 239000002243 precursor Substances 0.000 title claims abstract description 54
- 239000003054 catalyst Substances 0.000 title claims abstract description 36
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 17
- 150000004967 organic peroxy acids Chemical class 0.000 title claims abstract description 15
- -1 metal complex compounds Chemical class 0.000 title claims description 128
- 150000004965 peroxy acids Chemical class 0.000 title claims description 38
- 230000003647 oxidation Effects 0.000 title claims description 13
- 239000000203 mixture Substances 0.000 claims abstract description 89
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- 150000004696 coordination complex Chemical class 0.000 claims abstract description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 83
- 125000000217 alkyl group Chemical group 0.000 claims description 82
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 81
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- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 56
- 229910052757 nitrogen Inorganic materials 0.000 claims description 55
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 54
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 51
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- BGRWYDHXPHLNKA-UHFFFAOYSA-N Tetraacetylethylenediamine Chemical compound CC(=O)N(C(C)=O)CCN(C(C)=O)C(C)=O BGRWYDHXPHLNKA-UHFFFAOYSA-N 0.000 claims description 9
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- 125000003118 aryl group Chemical group 0.000 claims description 8
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- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical group [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 7
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- 229910052742 iron Inorganic materials 0.000 claims description 6
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- 150000002978 peroxides Chemical class 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 5
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
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- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- 239000010941 cobalt Substances 0.000 claims description 4
- 229910017052 cobalt Inorganic materials 0.000 claims description 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 4
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- 239000010949 copper Substances 0.000 claims description 4
- 238000011065 in-situ storage Methods 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 150000001538 azepines Chemical class 0.000 claims description 3
- 125000005544 phthalimido group Chemical group 0.000 claims description 3
- MHKLKWCYGIBEQF-UHFFFAOYSA-N 4-(1,3-benzothiazol-2-ylsulfanyl)morpholine Chemical compound C1COCCN1SC1=NC2=CC=CC=C2S1 MHKLKWCYGIBEQF-UHFFFAOYSA-N 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 229960001922 sodium perborate Drugs 0.000 claims description 2
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 70
- 238000003786 synthesis reaction Methods 0.000 description 52
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- 125000004356 hydroxy functional group Chemical group O* 0.000 description 45
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- JFJNVIPVOCESGZ-UHFFFAOYSA-N 2,3-dipyridin-2-ylpyridine Chemical compound N1=CC=CC=C1C1=CC=CN=C1C1=CC=CC=N1 JFJNVIPVOCESGZ-UHFFFAOYSA-N 0.000 description 21
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 21
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- HJKYXKSLRZKNSI-UHFFFAOYSA-I pentapotassium;hydrogen sulfate;oxido sulfate;sulfuric acid Chemical compound [K+].[K+].[K+].[K+].[K+].OS([O-])(=O)=O.[O-]S([O-])(=O)=O.OS(=O)(=O)O[O-].OS(=O)(=O)O[O-] HJKYXKSLRZKNSI-UHFFFAOYSA-I 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
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- SIOXPEMLGUPBBT-UHFFFAOYSA-M picolinate Chemical compound [O-]C(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-M 0.000 description 1
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
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- OKBMCNHOEMXPTM-UHFFFAOYSA-M potassium peroxymonosulfate Chemical group [K+].OOS([O-])(=O)=O OKBMCNHOEMXPTM-UHFFFAOYSA-M 0.000 description 1
- PSBAZVJEUNOIDU-UHFFFAOYSA-L potassium;sodium;diacetate Chemical class [Na+].[K+].CC([O-])=O.CC([O-])=O PSBAZVJEUNOIDU-UHFFFAOYSA-L 0.000 description 1
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- 125000000075 primary alcohol group Chemical group 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000003219 pyrazolines Chemical class 0.000 description 1
- BXEMXLDMNMKWPV-UHFFFAOYSA-N pyridine Chemical compound C1=CC=NC=C1.C1=CC=NC=C1 BXEMXLDMNMKWPV-UHFFFAOYSA-N 0.000 description 1
- KNXKVYCVGXFLES-UHFFFAOYSA-N pyridine-2-carboximidamide Chemical compound NC(=N)C1=CC=CC=N1 KNXKVYCVGXFLES-UHFFFAOYSA-N 0.000 description 1
- GMHCEDDZKAYPLB-UHFFFAOYSA-N pyridine-2-carboximidamide;hydrochloride Chemical compound [Cl-].NC(=[NH2+])C1=CC=CC=N1 GMHCEDDZKAYPLB-UHFFFAOYSA-N 0.000 description 1
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- 235000011083 sodium citrates Nutrition 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
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- IBDSNZLUHYKHQP-UHFFFAOYSA-N sodium;3-oxidodioxaborirane;tetrahydrate Chemical compound O.O.O.O.[Na+].[O-]B1OO1 IBDSNZLUHYKHQP-UHFFFAOYSA-N 0.000 description 1
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- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
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- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical class [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
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Classifications
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- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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- D—TEXTILES; PAPER
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-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2540/00—Compositional aspects of coordination complexes or ligands in catalyst systems
- B01J2540/10—Non-coordinating groups comprising only oxygen beside carbon or hydrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2540/00—Compositional aspects of coordination complexes or ligands in catalyst systems
- B01J2540/40—Non-coordinating groups comprising nitrogen
- B01J2540/42—Quaternary ammonium groups
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Textile Engineering (AREA)
- Medicinal Chemistry (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Catalysts (AREA)
- Epoxy Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04100078 | 2004-01-12 | ||
| PCT/EP2005/050000 WO2005068074A2 (en) | 2004-01-12 | 2005-01-03 | Use of metal complex compounds comprising pyridine pryimidine or s-triazne derived ligands as catalysts for oxidations with organic peroxy acids and/or precursors of organic peroxy acid and h2o2 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA06007817A true MXPA06007817A (es) | 2006-09-01 |
Family
ID=34778211
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA06007817A MXPA06007817A (es) | 2004-01-12 | 2005-01-03 | Uso de compuestos complejos de metales, que comprenden ligaduras derivadas de piridina-pirimidina o s-triazina como catalizadores para oxidaciones con acidos peroxi organicos y/o precursores de acidos peroxi organicos y h2o2. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20090189119A1 (enExample) |
| EP (1) | EP1703976A2 (enExample) |
| JP (1) | JP2007523973A (enExample) |
| KR (1) | KR20060126531A (enExample) |
| CN (1) | CN1929920A (enExample) |
| AU (1) | AU2005205064A1 (enExample) |
| BR (1) | BRPI0506799A (enExample) |
| MX (1) | MXPA06007817A (enExample) |
| WO (1) | WO2005068074A2 (enExample) |
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| JP2007534479A (ja) * | 2004-04-29 | 2007-11-29 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 硬質表面上の着色した汚れを漂白するためのパーオキシ化合物を用いた反応の触媒としての、ビスピリジルピリミジン又はビスピリジルトリアジン配位子を有する金属錯体の使用 |
| US20090044345A1 (en) * | 2006-02-06 | 2009-02-19 | Gunther Schlingloff | Use of Metal Complex Compounds as Oxidation Catalysts |
| EP1878733A1 (en) * | 2006-07-14 | 2008-01-16 | Novartis AG | Pyrimidine derivatives as ALK-5 inhibitors |
| WO2009000685A1 (en) * | 2007-06-25 | 2008-12-31 | Basf Se | Use of metal complex oxidation catalysts together with zinc compounds in laundry compositions |
| JP5270678B2 (ja) * | 2007-07-23 | 2013-08-21 | ビーエーエスエフ ソシエタス・ヨーロピア | 金属錯体化合物の酸化触媒としての使用 |
| DE102007034725A1 (de) | 2007-07-23 | 2009-01-29 | Henkel Kgaa | TOC-Abbau in Abwässern durch Übergangsmetallkatalysatoren |
| DE102007042615A1 (de) | 2007-09-07 | 2009-03-12 | Bk Giulini Gmbh | Erhöhung der bioziden Wirkung von Wasserstoffperoxid in Abwässern durch Übergangsmetallkatalysatoren |
| US20090325841A1 (en) | 2008-02-11 | 2009-12-31 | Ecolab Inc. | Use of activator complexes to enhance lower temperature cleaning in alkaline peroxide cleaning systems |
| EP2252683B1 (en) * | 2008-02-11 | 2015-07-15 | Ecolab Inc. | Use of activator complexes to enhance lower temperature cleaning in alkaline peroxide cleaning systems |
| EP2103735A1 (en) | 2008-03-18 | 2009-09-23 | Unilever PLC | Catalytic bleaching of substrates |
| CN101503242B (zh) * | 2009-03-13 | 2011-04-20 | 哈尔滨工业大学 | 利用中间态锰强化高锰酸钾除污染的水处理药剂 |
| US9511167B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
| US8778136B2 (en) | 2009-05-28 | 2014-07-15 | Gp Cellulose Gmbh | Modified cellulose from chemical kraft fiber and methods of making and using the same |
| US9512237B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Method for inhibiting the growth of microbes with a modified cellulose fiber |
| US9512563B2 (en) | 2009-05-28 | 2016-12-06 | Gp Cellulose Gmbh | Surface treated modified cellulose from chemical kraft fiber and methods of making and using same |
| CA2775969C (en) * | 2009-11-17 | 2016-12-20 | Novartis Ag | A hydrogen peroxide solution and kit for disinfecting contact lenses |
| KR20120114287A (ko) * | 2009-12-02 | 2012-10-16 | 바스프 에스이 | 포장 용도를 위한 산소 흡수제/제거제 부재로서 금속 착물의 용도 |
| TWI558439B (zh) * | 2010-04-26 | 2016-11-21 | 三菱瓦斯化學股份有限公司 | 含過硫酸鹽及銀錯合物之化學物質分解用處理劑及使用該處理劑之化學物質分解方法 |
| US8877353B2 (en) * | 2010-07-21 | 2014-11-04 | Versitech Limited | Platinum (II) tetradentate ONCN complexes for organic light-emitting diode applications |
| WO2012170183A1 (en) | 2011-05-23 | 2012-12-13 | Gp Cellulose Gmbh | Softwood kraft fiber having improved whiteness and brightness and methods of making and using the same |
| PT2753627T (pt) * | 2011-09-08 | 2018-10-22 | Catexel Tech Limited | Catalisadores |
| CN103174006A (zh) * | 2011-11-24 | 2013-06-26 | 东华大学 | 双吡啶嘧啶金属配合物在纺织品低温练漂助剂中的应用 |
| CN103194896A (zh) * | 2011-11-24 | 2013-07-10 | 东华大学 | 三联吡啶金属配合物在纺织品低温练漂助剂中的应用 |
| KR102093167B1 (ko) | 2012-01-12 | 2020-03-26 | 게페 첼루로제 게엠베하 | 황변 성질이 감소된 저 점성 크래프트 섬유 및 그의 제조 및 사용 방법 |
| US9617686B2 (en) | 2012-04-18 | 2017-04-11 | Gp Cellulose Gmbh | Use of surfactant to treat pulp and improve the incorporation of kraft pulp into fiber for the production of viscose and other secondary fiber products |
| RU2018117289A (ru) | 2013-02-08 | 2018-10-26 | ДжиПи СЕЛЛЬЮЛОУС ГМБХ | КРАФТ-ВОЛОКНО ДРЕВЕСИНЫ ХВОЙНЫХ ПОРОД С УЛУЧШЕННЫМ СОДЕРЖАНИЕМ α-ЦЕЛЛЮЛОЗЫ И ЕГО ПРИМЕНЕНИЕ ПРИ ПРОИЗВОДСТВЕ ХИМИЧЕСКИХ ЦЕЛЛЮЛОЗНЫХ ПРОДУКТОВ |
| RU2671653C2 (ru) | 2013-03-14 | 2018-11-06 | ДжиПи СЕЛЛЬЮЛОУС ГМБХ | Способ изготовления высокофункционального маловязкого крафтволокна с использованием последовательности кислотного отбеливания и волокно, изготовленное с помощью этого процесса |
| MX372579B (es) | 2013-03-15 | 2020-04-17 | Gp Cellulose Gmbh | Una fibra kraft de baja viscosidad que tiene un contenido de carboxilo mejorado, y metodos para fabricar y usar la misma |
| BR112016003054B1 (pt) | 2013-08-16 | 2022-02-15 | Chemsenti Limited | Formulação de branqueamento, partícula, método e uso de uma partícula |
| WO2016052196A1 (ja) * | 2014-09-29 | 2016-04-07 | 富士フイルム株式会社 | 光電変換素子、色素増感太陽電池、金属錯体色素、色素溶液、およびターピリジン化合物またはそのエステル化物 |
| WO2016052193A1 (ja) * | 2014-09-29 | 2016-04-07 | 富士フイルム株式会社 | 光電変換素子、色素増感太陽電池、金属錯体色素、色素溶液、およびターピリジン化合物またはそのエステル化物 |
| CN105369581A (zh) * | 2015-11-04 | 2016-03-02 | 泉州市新宏化工贸易有限公司 | 一种棉织物练漂后除氧工艺及棉洁爽 |
| CN106478745B (zh) * | 2016-10-14 | 2019-02-05 | 高介平 | 一种无甲醛水性交联剂及其制备方法和对织物的整理工艺 |
| EP3541849B1 (en) | 2016-11-16 | 2023-11-15 | GP Cellulose GmbH | Modified cellulose from chemical fiber and methods of making and using the same |
| EP3967742A1 (en) | 2020-09-15 | 2022-03-16 | WeylChem Performance Products GmbH | Compositions comprising bleaching catalyst, manufacturing process thereof, and bleaching and cleaning agent comprising same |
| CN114887663B (zh) * | 2022-05-03 | 2023-05-12 | 东华大学 | 一种产生单线态氧的催化系统及其应用 |
| CN115634716A (zh) * | 2022-10-20 | 2023-01-24 | 金宏气体股份有限公司 | 光催化剂、其制备方法、光催化体系及应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3912648A (en) * | 1973-03-21 | 1975-10-14 | American Cyanamid Co | Ring halogen-free substituted triazine compounds as bleach activators |
| US5268477A (en) * | 1985-09-12 | 1993-12-07 | The Upjohn Company | Triazinylpiperazinyl amine intermediates |
| AU6357896A (en) * | 1996-06-19 | 1998-01-07 | Hans-Peter Call | Multicomponent system for use with detergent substances |
| DE19726241A1 (de) * | 1997-06-20 | 1998-12-24 | Call Krimhild | Erweitertes enzymatisches Multikomponentensystem zur Behandlung von Abwässern, zur Herstellung von Holzverbundstoffen, zum Deinken von Altpapier, Colour stripping von Altpapier, zum Einsatz als Oxidationssystem bei der organischen Synthese und zum Einsatz bei der Kohleverflüssigung |
| JPH1150096A (ja) * | 1997-08-01 | 1999-02-23 | Lion Corp | 自動食器洗浄機用粒状洗浄剤組成物 |
| ATE315627T1 (de) * | 1999-07-14 | 2006-02-15 | Ciba Sc Holding Ag | Metallkomplexe von tripodalenliganden |
| CN1426451A (zh) * | 2000-02-29 | 2003-06-25 | 荷兰联合利华有限公司 | 漂白底物的组合物和方法 |
| JP3605012B2 (ja) * | 2000-08-11 | 2004-12-22 | 独立行政法人科学技術振興機構 | オレフィンの酸化的分解によるケトンの製造法 |
| DE60211884T2 (de) * | 2001-04-30 | 2006-11-23 | Ciba Speciality Chemicals Holding Inc. | Verwendung von metallkomplexverbindungen als oxidationskatalysatoren |
| EP1556467B1 (en) * | 2002-10-30 | 2006-07-05 | Ciba SC Holding AG | Use of metal complex compounds as oxidation catalysts |
| WO2004104155A1 (en) * | 2003-05-21 | 2004-12-02 | Ciba Specialty Chemicals Holding Inc. | Stable particulate composition comprising bleach catalysts |
-
2005
- 2005-01-03 BR BRPI0506799-5A patent/BRPI0506799A/pt not_active IP Right Cessation
- 2005-01-03 CN CNA2005800074023A patent/CN1929920A/zh active Pending
- 2005-01-03 AU AU2005205064A patent/AU2005205064A1/en not_active Abandoned
- 2005-01-03 EP EP05701417A patent/EP1703976A2/en not_active Withdrawn
- 2005-01-03 KR KR1020067013458A patent/KR20060126531A/ko not_active Withdrawn
- 2005-01-03 MX MXPA06007817A patent/MXPA06007817A/es unknown
- 2005-01-03 US US10/585,543 patent/US20090189119A1/en not_active Abandoned
- 2005-01-03 WO PCT/EP2005/050000 patent/WO2005068074A2/en not_active Ceased
- 2005-01-03 JP JP2006548291A patent/JP2007523973A/ja not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0506799A (pt) | 2007-05-22 |
| AU2005205064A1 (en) | 2005-07-28 |
| JP2007523973A (ja) | 2007-08-23 |
| CN1929920A (zh) | 2007-03-14 |
| WO2005068074A2 (en) | 2005-07-28 |
| KR20060126531A (ko) | 2006-12-07 |
| US20090189119A1 (en) | 2009-07-30 |
| WO2005068074A3 (en) | 2006-05-18 |
| EP1703976A2 (en) | 2006-09-27 |
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