KR20150013273A - 높은 4차화도를 가진 4차화된 폴리에틸렌이민 - Google Patents
높은 4차화도를 가진 4차화된 폴리에틸렌이민 Download PDFInfo
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- KR20150013273A KR20150013273A KR1020147034664A KR20147034664A KR20150013273A KR 20150013273 A KR20150013273 A KR 20150013273A KR 1020147034664 A KR1020147034664 A KR 1020147034664A KR 20147034664 A KR20147034664 A KR 20147034664A KR 20150013273 A KR20150013273 A KR 20150013273A
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- 229920002873 Polyethylenimine Polymers 0.000 title claims abstract description 49
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- 239000000203 mixture Substances 0.000 claims description 233
- 125000000217 alkyl group Chemical group 0.000 claims description 54
- 229910052757 nitrogen Inorganic materials 0.000 claims description 35
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- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
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- 238000000034 method Methods 0.000 description 12
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
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- QPCDCPDFJACHGM-UHFFFAOYSA-K pentetate(3-) Chemical compound OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O QPCDCPDFJACHGM-UHFFFAOYSA-K 0.000 description 1
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- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
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- BITYAPCSNKJESK-UHFFFAOYSA-N potassiosodium Chemical compound [Na].[K] BITYAPCSNKJESK-UHFFFAOYSA-N 0.000 description 1
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- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- OKBMCNHOEMXPTM-UHFFFAOYSA-M potassium peroxymonosulfate Chemical compound [K+].OOS([O-])(=O)=O OKBMCNHOEMXPTM-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
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- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
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- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
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- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
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- 238000005670 sulfation reaction Methods 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
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- 239000000725 suspension Substances 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- DCQJDRNKCUQEMA-UHFFFAOYSA-N tetradecanediperoxoic acid Chemical compound OOC(=O)CCCCCCCCCCCCC(=O)OO DCQJDRNKCUQEMA-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
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- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical class OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
- C08G73/0226—Quaternisation of polyalkylene(poly)amines
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3723—Polyamines or polyalkyleneimines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Detergent Compositions (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Cosmetics (AREA)
- Polyethers (AREA)
- Paper (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12167675.3 | 2012-05-11 | ||
| EP12167675 | 2012-05-11 | ||
| PCT/EP2013/059170 WO2013167467A1 (en) | 2012-05-11 | 2013-05-02 | Quaternized polyethylenimines with a high quaternization degree |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20150013273A true KR20150013273A (ko) | 2015-02-04 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| KR1020147034664A Ceased KR20150013273A (ko) | 2012-05-11 | 2013-05-02 | 높은 4차화도를 가진 4차화된 폴리에틸렌이민 |
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|---|---|
| EP (1) | EP2847252B1 (enExample) |
| JP (1) | JP6250640B2 (enExample) |
| KR (1) | KR20150013273A (enExample) |
| CN (1) | CN104321364B (enExample) |
| BR (1) | BR112014027872B1 (enExample) |
| CA (1) | CA2871020A1 (enExample) |
| ES (1) | ES2626505T3 (enExample) |
| MX (1) | MX2014013743A (enExample) |
| PH (1) | PH12014502519A1 (enExample) |
| PL (1) | PL2847252T3 (enExample) |
| RU (1) | RU2631860C2 (enExample) |
| WO (1) | WO2013167467A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX358348B (es) * | 2012-05-11 | 2018-08-15 | Basf Se | Polietileniminas cuaternizadas con un alto grado de etoxilacion. |
| EP3098296A1 (en) * | 2015-05-29 | 2016-11-30 | The Procter and Gamble Company | Process for making a multi-compartment pouch |
| CN108026482B (zh) * | 2015-07-06 | 2021-06-18 | 艺康美国股份有限公司 | 通过新颖氧化剂和螯合剂的组合去除污渍 |
| CA3018930A1 (en) * | 2016-04-08 | 2017-10-12 | The Procter & Gamble Company | Automatic dishwashing cleaning composition |
| JP6715107B2 (ja) * | 2016-06-30 | 2020-07-01 | ライオン株式会社 | 液体洗浄剤組成物 |
| WO2018029021A1 (en) * | 2016-08-08 | 2018-02-15 | Basf Se | Liquid laundry formulation |
| ES2992830T3 (en) | 2018-08-10 | 2024-12-18 | Basf Se | Process for manufacturing alkoxylated polyethyleneimines |
| CN114007753A (zh) * | 2019-07-24 | 2022-02-01 | 巴斯夫欧洲公司 | 捕收剂组合物 |
| EP3862412A1 (en) * | 2020-02-04 | 2021-08-11 | The Procter & Gamble Company | Detergent composition |
| JP7063954B2 (ja) * | 2020-07-29 | 2022-05-09 | エコラボ ユーエスエー インコーポレイティド | 新規の酸化剤とキレート剤の組み合わせによる染み除去 |
| JP2023027957A (ja) * | 2021-08-18 | 2023-03-03 | 株式会社日本触媒 | ポリアルキレンイミン誘導体組成物 |
| WO2024014555A1 (ja) * | 2022-07-15 | 2024-01-18 | ライオン株式会社 | 食器用の液体洗浄剤組成物 |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB30255A (enExample) * | 1968-06-25 | |||
| US3812044A (en) | 1970-12-28 | 1974-05-21 | Procter & Gamble | Detergent composition containing a polyfunctionally-substituted aromatic acid sequestering agent |
| CA995092A (en) | 1972-07-03 | 1976-08-17 | Rodney M. Wise | Sulfated alkyl ethoxylate-containing detergent composition |
| GB2048606B (en) | 1979-02-28 | 1983-03-16 | Barr & Stroud Ltd | Optical scanning system |
| EP0111965B1 (en) * | 1982-12-23 | 1989-07-26 | THE PROCTER & GAMBLE COMPANY | Detergent compositions containing cationic compounds having clay soil removal/anti-redeposition properties |
| US4663071A (en) | 1986-01-30 | 1987-05-05 | The Procter & Gamble Company | Ether carboxylate detergent builders and process for their preparation |
| GB8629837D0 (en) | 1986-12-13 | 1987-01-21 | Interox Chemicals Ltd | Bleach activation |
| GB8908416D0 (en) | 1989-04-13 | 1989-06-01 | Unilever Plc | Bleach activation |
| DE69125309T2 (de) | 1990-05-21 | 1997-07-03 | Unilever Nv | Bleichmittelaktivierung |
| GB9108136D0 (en) | 1991-04-17 | 1991-06-05 | Unilever Plc | Concentrated detergent powder compositions |
| EG21623A (en) | 1996-04-16 | 2001-12-31 | Procter & Gamble | Mid-chain branced surfactants |
| PH11997056158B1 (en) | 1996-04-16 | 2001-10-15 | Procter & Gamble | Mid-chain branched primary alkyl sulphates as surfactants |
| EG22088A (en) | 1996-04-16 | 2002-07-31 | Procter & Gamble | Alkoxylated sulfates |
| DE69732216T2 (de) | 1997-02-14 | 2005-12-08 | The Procter & Gamble Company, Cincinnati | Flüssige Reinigungsmittelzusammensetzungen für harte Oberflächen |
| ID28110A (id) | 1997-07-21 | 2001-05-03 | Procter & Gamble | Surfaktan alkilbenzenasulfonat yang disempurnakan |
| AU8124398A (en) | 1997-07-21 | 1999-02-16 | Procter & Gamble Company, The | Process for making alkylbenzenesulfonate surfactants from alcohols and products thereof |
| PH11998001775B1 (en) | 1997-07-21 | 2004-02-11 | Procter & Gamble | Improved alkyl aryl sulfonate surfactants |
| EP1002028A1 (en) | 1997-07-21 | 2000-05-24 | The Procter & Gamble Company | Cleaning products comprising improved alkylarylsulfonate surfactants prepared via vinylidene olefins and processes for preparation thereof |
| ZA986443B (en) | 1997-07-21 | 1999-01-21 | Procter & Gamble | Processes for making alkylbenzenesulfonate surfactants and products thereof |
| ES2195358T3 (es) | 1997-07-21 | 2003-12-01 | Procter & Gamble | Composiciones detergentes que contienen mezclas de tensioactivos de cristalinidad desorganizada. |
| GB2327947A (en) | 1997-08-02 | 1999-02-10 | Procter & Gamble | Detergent tablet |
| EP1027312B1 (en) | 1997-08-08 | 2005-01-12 | The Procter & Gamble Company | Improved processes for making surfactants via adsorptive separation |
| ES2238753T3 (es) | 1998-05-15 | 2005-09-01 | THE PROCTER & GAMBLE COMPANY | Composicion liquida acida para limpiar superficies duras. |
| CA2346690C (en) | 1998-10-20 | 2003-12-16 | Jeffrey John Scheibel | Laundry detergents comprising modified alkylbenzene sulfonates |
| US6514926B1 (en) | 1998-10-20 | 2003-02-04 | The Procter & Gamble Company | Laundry detergents comprising modified alkylbenzene sulfonates |
| US7326677B2 (en) * | 2003-07-11 | 2008-02-05 | The Procter & Gamble Company | Liquid laundry detergent compositions comprising a silicone blend of non-functionalized and amino-functionalized silicone polymers |
| CA2549565A1 (en) * | 2003-12-19 | 2005-07-14 | The Procter & Gamble Company | Hydrophobic polyamine ethoxylates |
| CA2602128C (en) | 2005-04-15 | 2012-08-07 | The Procter & Gamble Company | Cleaning compositions with alkoxylated polyalkylenimines |
| PL1869155T3 (pl) * | 2005-04-15 | 2011-03-31 | Procter & Gamble | Ciekłe kompozycje detergentu do prania ze zmodyfikowanymi polimerami polietylenoiminy oraz enzymem lipazy |
| CA2652799C (en) | 2006-05-22 | 2013-01-08 | The Procter & Gamble Company | Liquid detergent composition for improved grease cleaning |
| EP2014755B1 (en) * | 2007-05-29 | 2012-03-21 | The Procter & Gamble Company | Method of cleaning dishware |
| PL2209837T3 (pl) * | 2007-11-09 | 2020-02-28 | Basf Se | Amfifilowe rozpuszczalne w wodzie alkoksylowane polialkilenoiminy zawierające wewnętrzny blok poli(tlenku etylenu) i zewnętrzny blok poli(tlenku propylenu) |
| GB0815022D0 (en) | 2008-08-16 | 2008-09-24 | Reckitt Benckiser Nv | Composition |
| GB0919097D0 (en) | 2009-10-30 | 2009-12-16 | Croda Int Plc | Treatment of hard surfaces |
| CN103003476B (zh) * | 2010-07-02 | 2016-02-10 | 宝洁公司 | 纤维网材料以及用于制造纤维网材料的方法 |
-
2013
- 2013-05-02 BR BR112014027872-5A patent/BR112014027872B1/pt not_active IP Right Cessation
- 2013-05-02 WO PCT/EP2013/059170 patent/WO2013167467A1/en not_active Ceased
- 2013-05-02 EP EP13723040.5A patent/EP2847252B1/en active Active
- 2013-05-02 RU RU2014149839A patent/RU2631860C2/ru active
- 2013-05-02 MX MX2014013743A patent/MX2014013743A/es unknown
- 2013-05-02 CN CN201380023846.0A patent/CN104321364B/zh not_active Expired - Fee Related
- 2013-05-02 ES ES13723040.5T patent/ES2626505T3/es active Active
- 2013-05-02 PL PL13723040T patent/PL2847252T3/pl unknown
- 2013-05-02 CA CA2871020A patent/CA2871020A1/en not_active Abandoned
- 2013-05-02 KR KR1020147034664A patent/KR20150013273A/ko not_active Ceased
- 2013-05-02 JP JP2015510748A patent/JP6250640B2/ja not_active Expired - Fee Related
-
2014
- 2014-11-11 PH PH12014502519A patent/PH12014502519A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BR112014027872A2 (pt) | 2017-06-27 |
| ES2626505T3 (es) | 2017-07-25 |
| EP2847252B1 (en) | 2017-03-08 |
| PL2847252T3 (pl) | 2017-08-31 |
| JP6250640B2 (ja) | 2017-12-20 |
| EP2847252A1 (en) | 2015-03-18 |
| WO2013167467A1 (en) | 2013-11-14 |
| BR112014027872B1 (pt) | 2020-11-24 |
| CN104321364B (zh) | 2016-11-16 |
| CA2871020A1 (en) | 2013-11-14 |
| RU2014149839A (ru) | 2016-07-10 |
| MX2014013743A (es) | 2015-09-16 |
| RU2631860C2 (ru) | 2017-09-27 |
| JP2015523420A (ja) | 2015-08-13 |
| PH12014502519A1 (en) | 2015-01-12 |
| CN104321364A (zh) | 2015-01-28 |
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