KR20110099714A - 분지형 단쇄 성분 및 분지형 장쇄 성분을 포함하는 계면활성제 혼합물 - Google Patents
분지형 단쇄 성분 및 분지형 장쇄 성분을 포함하는 계면활성제 혼합물 Download PDFInfo
- Publication number
- KR20110099714A KR20110099714A KR1020117015442A KR20117015442A KR20110099714A KR 20110099714 A KR20110099714 A KR 20110099714A KR 1020117015442 A KR1020117015442 A KR 1020117015442A KR 20117015442 A KR20117015442 A KR 20117015442A KR 20110099714 A KR20110099714 A KR 20110099714A
- Authority
- KR
- South Korea
- Prior art keywords
- alkanol
- mixture
- surfactant
- weight
- alkoxylation
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 262
- 239000004094 surface-active agent Substances 0.000 title claims abstract description 124
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- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 53
- 238000009472 formulation Methods 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 39
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- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims abstract description 5
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- 239000003599 detergent Substances 0.000 claims description 39
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- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 12
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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 description 10
- 239000003945 anionic surfactant Substances 0.000 description 10
- XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical class [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 10
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- 150000003839 salts Chemical class 0.000 description 9
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- 230000015572 biosynthetic process Effects 0.000 description 8
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- 238000002360 preparation method Methods 0.000 description 8
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- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 7
- 239000012190 activator Substances 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 7
- IAQRGUVFOMOMEM-UHFFFAOYSA-N but-2-ene Chemical compound CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 7
- 229910000001 cobalt(II) carbonate Inorganic materials 0.000 description 7
- 238000007046 ethoxylation reaction Methods 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 229910052708 sodium Inorganic materials 0.000 description 7
- 229920001567 vinyl ester resin Polymers 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 6
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- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
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- 229910052700 potassium Inorganic materials 0.000 description 6
- QEVWDMOIPOLQBL-UHFFFAOYSA-N 5-methyl-2-propylhexan-1-ol Chemical compound CCCC(CO)CCC(C)C QEVWDMOIPOLQBL-UHFFFAOYSA-N 0.000 description 5
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
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- 238000012360 testing method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/825—Mixtures of compounds all of which are non-ionic
- C11D1/8255—Mixtures of compounds all of which are non-ionic containing a combination of compounds differently alcoxylised or with differently alkylated chains
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/017—Mixtures of compounds
- C09K23/018—Mixtures of two or more different organic oxygen-containing compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08172067 | 2008-12-18 | ||
| EP08172067.4 | 2008-12-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20110099714A true KR20110099714A (ko) | 2011-09-08 |
Family
ID=42077084
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020117015442A Abandoned KR20110099714A (ko) | 2008-12-18 | 2009-12-18 | 분지형 단쇄 성분 및 분지형 장쇄 성분을 포함하는 계면활성제 혼합물 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20110260101A1 (enExample) |
| EP (1) | EP2379690A1 (enExample) |
| JP (1) | JP5575146B2 (enExample) |
| KR (1) | KR20110099714A (enExample) |
| CN (1) | CN102257110B (enExample) |
| AR (1) | AR074787A1 (enExample) |
| TW (1) | TW201031743A (enExample) |
| WO (1) | WO2010070088A1 (enExample) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011003904A1 (de) * | 2009-07-10 | 2011-01-13 | Basf Se | Tensidgemisch mit kurz- und langkettigen komponenten |
| US9062278B2 (en) | 2010-02-19 | 2015-06-23 | Basf Se | Preparing ether carboxylates |
| JP5852648B2 (ja) | 2010-07-15 | 2016-02-03 | ザ プロクター アンド ギャンブルカンパニー | 鎖端付近分枝型化合物（ｎｅａｒｔｅｒｍｉｎａｌ−ｂｒａｎｃｈｅｄｃｏｍｐｏｕｎｄ）を含む組成物及びその製造方法 |
| US9070632B2 (en) | 2010-10-07 | 2015-06-30 | Basf Se | Aqueous polishing composition and process for chemically mechanically polishing substrates having patterned or unpatterned low-k dielectric layers |
| EP2457890A1 (en) | 2010-11-29 | 2012-05-30 | Cognis IP Management GmbH | Biocide compositions comprising alkoxylation products of isoamyl alcohol derivatives |
| CN103826734B (zh) * | 2011-09-27 | 2016-02-10 | 陶氏环球技术有限责任公司 | 支化烷氧基化物表面活性剂组合物 |
| JP2013212995A (ja) * | 2012-03-30 | 2013-10-17 | Idemitsu Kosan Co Ltd | オレフィン重合体の製造方法 |
| CA2870500A1 (en) * | 2012-05-10 | 2013-11-14 | Basf Se | Alkoxylated alcohols and their use in formulations for hard surface cleaning |
| EP2679607A1 (en) * | 2012-06-25 | 2014-01-01 | Basf Se | Process for emulsion polymerization |
| CN104861092B (zh) * | 2013-07-30 | 2016-06-29 | 浙江大学 | 反应型油脂基可降解表面活性剂的应用 |
| CN105658780B (zh) * | 2013-10-23 | 2019-04-05 | 荒川化学工业株式会社 | 工业用共沸清洗剂、物品的清洗方法、工业用共沸清洗剂的再生方法以及清洗再生装置 |
| AU2015305912B2 (en) * | 2014-08-22 | 2018-11-22 | Rohm And Haas Company | Imidazole-modified carbohydrate polymers as laundry dye transfer inhibitors |
| TN2017000094A1 (en) * | 2014-09-18 | 2018-07-04 | Akzo Nobel Chemicals Int Bv | Use of branched alcohols and alkoxylates thereof as secondary collectors. |
| EP3197991B1 (en) * | 2014-09-24 | 2020-05-27 | Dow Global Technologies LLC | Branched biodegradable low foam nonionic surfactants |
| US10550354B2 (en) | 2015-05-19 | 2020-02-04 | Ecolab Usa Inc. | Efficient surfactant system on plastic and all types of ware |
| WO2017198438A1 (en) | 2016-05-17 | 2017-11-23 | Unilever Plc | Liquid laundry detergent compositions |
| WO2018197476A1 (en) | 2017-04-25 | 2018-11-01 | Basf Se | Collectors for beneficiation of phosphate from phosphate containing ores |
| MX2021000999A (es) | 2018-07-25 | 2021-04-13 | Ecolab Usa Inc | Formulacion de abrillantador para la limpieza de piezas de automovil. |
| EP3917676A1 (en) | 2019-02-01 | 2021-12-08 | Basf Se | Mixture of fatty acids and alkylether phosphates as a collector for phosphate ore flotation |
| US11186805B2 (en) | 2019-12-20 | 2021-11-30 | The Procter & Gamble Company | Particulate fabric care composition |
| US20230227727A1 (en) * | 2020-05-29 | 2023-07-20 | Dow Global Technologies Llc | Composition with Mixed C8-C18 Alcohols and Surfactants Thereof |
| CA3199907A1 (en) * | 2021-06-24 | 2022-12-29 | Francesco BARBERO | Colour care detergent compositions |
| EP4108749A1 (en) * | 2021-06-24 | 2022-12-28 | The Procter & Gamble Company | Colour care detergent compositions |
| CA3260784A1 (en) | 2022-07-11 | 2024-01-18 | The Procter & Gamble Company | LAUNDRY DETERGENT COMPOSITION CONTAINING A GRAFTED COPOLYMER AND A BENEFICIAL AGENT |
| PL442556A1 (pl) * | 2022-10-18 | 2024-04-22 | Sieć Badawcza Łukasiewicz - Instytut Ciężkiej Syntezy Organicznej Blachownia | Preparat do mycia owoców i warzyw i sposób stosowania preparatu do mycia owoców i warzyw |
| PL442558A1 (pl) * | 2022-10-18 | 2024-04-22 | Sieć Badawcza Łukasiewicz - Instytut Ciężkiej Syntezy Organicznej Blachownia | Preparat do mycia owoców i warzyw i sposób stosowania preparatu do mycia owoców i warzyw |
Family Cites Families (85)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2965678A (en) * | 1951-12-28 | 1960-12-20 | Gen Aniline & Film Corp | Polyoxyethylene ethers of branched chain alcohols |
| US2768894A (en) * | 1954-04-30 | 1956-10-30 | Gen Aniline & Film Corp | Photographic element with emulsion layer containing color former and wetting agent |
| GB1088984A (en) | 1963-06-05 | 1967-10-25 | Ici Ltd | Modifying treatment of shaped articles derived from polyesters |
| GB1154730A (en) | 1965-10-08 | 1969-06-11 | Ici Ltd | Improvements in the Laundering of Synthetic Polymeric Textile Materials |
| DE1568542C3 (de) | 1966-06-15 | 1974-07-18 | Bayer Ag, 5090 Leverkusen | Verfahren zur katalytischen Umwandlung von Butadien- und n-Buten-1-haltigen C tief 4 - Kohlenwasserstoffen |
| US3887806A (en) | 1973-10-09 | 1975-06-03 | Crown Cork & Seal Co | Faulty can detector |
| US4604224A (en) | 1975-12-15 | 1986-08-05 | Colgate Palmolive Co. | Zeolite containing heavy duty non-phosphate detergent composition |
| ES472603A1 (es) | 1977-08-22 | 1979-10-16 | Monsanto Co | Un procedimiento para preparar un polimero de carboxilato deacetal |
| DE2902236A1 (de) | 1978-01-25 | 1979-07-26 | Kao Corp | Bleichmittelmischung |
| EP0016286B1 (en) | 1979-03-21 | 1983-04-06 | DAVY McKEE (LONDON) LIMITED | Hydroformylation process |
| EP0021491A1 (en) | 1979-06-18 | 1981-01-07 | THE PROCTER & GAMBLE COMPANY | Detergent containing nonionic/cationic surfactant and builder mixture |
| US4287080A (en) * | 1979-09-17 | 1981-09-01 | The Procter & Gamble Company | Detergent compositions which contain certain tertiary alcohols |
| US4265777A (en) | 1980-04-17 | 1981-05-05 | The Procter & Gamble Company | Detergent compositions containing an aluminosilicate detergency builder and an unsaturated fatty acid soap |
| DE3039770A1 (de) | 1980-10-22 | 1982-05-27 | Basf Ag, 6700 Ludwigshafen | Verwendung von alkoxylierten verbindungen als nichtionische emulgatorkomponente in pflanzenschutzmittelformulierungen |
| DE3143647A1 (de) | 1981-11-04 | 1983-05-11 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur selektiven hydrierung von mehrfach ungesaettigten kohlenwasserstoffen in kohlenwasserstoff-gemischen |
| EP0087035B1 (en) | 1982-02-08 | 1985-09-11 | Union Carbide Corporation | Zeolite-containing detergent compositions and process for preparing same |
| EP0185427B1 (en) | 1984-12-21 | 1992-03-04 | The Procter & Gamble Company | Block polyesters and like compounds useful as soil release agents in detergent compositions |
| DE3536530A1 (de) | 1985-10-12 | 1987-04-23 | Basf Ag | Verwendung von pfropfcopolymerisaten aus polyalkylenoxiden und vinylacetat als vergrauungsinhibitoren beim waschen und nachbehandeln von synthesefasern enthaltendem textilgut |
| US4711730A (en) | 1986-04-15 | 1987-12-08 | The Procter & Gamble Company | Capped 1,2-propylene terephthalate-polyoxyethylene terephthalate polyesters useful as soil release agents |
| US4713194A (en) | 1986-04-15 | 1987-12-15 | The Procter & Gamble Company | Block polyester and like compounds having branched hydrophilic capping groups useful as soil release agents in detergent compositions |
| FR2605635B1 (fr) * | 1986-10-27 | 1992-02-21 | Sandoz Sa | Nouveaux esters partiels de l'acide phosphorique, leur preparation et leur utilisation pour le pre-traitement des matieres textiles |
| GB8629936D0 (en) | 1986-12-15 | 1987-01-28 | Procter & Gamble | Laundry compositions |
| DE3711298A1 (de) | 1987-04-03 | 1988-10-13 | Basf Ag | Verwendung von propfpolymerisaten auf basis von polyalkylenoxiden als vergrauungsinhibitoren beim waschen und nachbehandeln von synthesefasern enthaltendem textilgut |
| DE3711318A1 (de) | 1987-04-03 | 1988-10-20 | Basf Ag | Verwendung von pfropfpolymerisaten auf basis von polyalkylenoxiden als vergrauungsinhibitoren beim waschen und nachbehandeln von synthesefasern enthaltendem textilgut |
| DE3711319A1 (de) | 1987-04-03 | 1988-10-20 | Basf Ag | Verwendung von pfropfpolymerisaten auf basis von polyalkylenoxiden als vergrauungsinhibitoren beim waschen und nachbehandeln von synthesefasern enthaltendem textilgut |
| DE3711299C2 (de) | 1987-04-03 | 1995-07-20 | Basf Ag | Verwendung von Pfropfpolymerisaten auf Basis von Polyvinylpyrrolidon als Vergrauungsinhibitoren beim Waschen und Nachbehandeln von Synthesefasern enthaltendem Textilgut |
| DE3712069A1 (de) | 1987-04-09 | 1988-10-20 | Basf Ag | Verwendung von pfropfpolymerisaten auf basis von polyestern, polyesterurethanen und polyesteramiden als vergrauungsinhibitoren in waschmitteln |
| CA2001927C (en) | 1988-11-03 | 1999-12-21 | Graham Thomas Brown | Aluminosilicates and detergent compositions |
| US5259963A (en) * | 1989-01-12 | 1993-11-09 | Sandoz Ltd. | Surface active compositions their production and use |
| DE69015424T2 (de) | 1989-04-28 | 1995-08-17 | Nippon Catalytic Chem Ind | Verfahren zur Herstellung und Verwendung von Salzen von Polymeren der Maleinsäure mit verbesserter Biodegradabilität. |
| DE4001415A1 (de) | 1990-01-19 | 1991-07-25 | Basf Ag | Polyester, die nichtionische tenside einkondensiert enthalten, ihre herstellung und ihre verwendung in waschmitteln |
| DE4003172A1 (de) | 1990-02-03 | 1991-08-08 | Basf Ag | Pfropfcopolymerisate von monosacchariden, oligosacchariden, polysacchariden und modifizierten polysacchariden, verfahren zu ihrer herstellung und ihre verwendung |
| US5041232A (en) | 1990-03-16 | 1991-08-20 | Lever Brothers Company, Division Of Conopco, Inc. | Sulfonimines as bleach catalysts |
| DE4008696A1 (de) | 1990-03-17 | 1991-09-19 | Basf Ag | Verfahren zur herstellung von homo- und copolymerisaten monoethylenisch ungesaettigter dicarbonsaeuren und ihre verwendung |
| IT1240684B (it) | 1990-04-26 | 1993-12-17 | Tecnopart Srl | Poliamminoacidi quali builders per formulazioni detergenti |
| DE4106354A1 (de) | 1991-02-28 | 1992-09-03 | Basf Ag | Polyacetale, verfahren zu ihrer herstellung und ihre verwendung in wasch- und reinigungsmitteln |
| DE4106355A1 (de) | 1991-02-28 | 1992-09-03 | Basf Ag | Verfahren zur herstellung von polyglyoxylaten |
| JP2614149B2 (ja) * | 1991-03-11 | 1997-05-28 | 富士写真フイルム株式会社 | 新規アルキルホスフェート |
| DE4108626A1 (de) | 1991-03-16 | 1992-09-17 | Basf Ag | Citronensaeure-ester von polyhydroxyverbindungen und ihre verwendung in wasch- und reinigungsmitteln |
| FR2675153B1 (fr) | 1991-04-15 | 1994-07-22 | Rhone Poulenc Chimie | Composition detergente contenant un biopolymere polyimide hydrolysable en milieu lessiviel. |
| GB9113674D0 (en) | 1991-06-25 | 1991-08-14 | Unilever Plc | Detergent compositions |
| GB9207756D0 (en) | 1992-04-07 | 1992-05-27 | Davy Mckee London | Process |
| DE4213282A1 (de) | 1992-04-23 | 1993-10-28 | Basf Ag | Verfahren zur Herstellung von Polyestern aus Citronensäure und Polyhydroxyverbindungen und ihre Verwendung |
| DE4221875A1 (de) | 1992-07-03 | 1994-01-05 | Basf Ag | Modifizierte Polyasparaginsäuren, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US5266237A (en) | 1992-07-31 | 1993-11-30 | Rohm And Haas Company | Enhancing detergent performance with polysuccinimide |
| DE4228159A1 (de) | 1992-08-25 | 1994-03-03 | Basf Ag | Verfahren zur Herstellung von Polyacetalen, ihre Verwendung und neue Polyacetale |
| DE4237178A1 (de) | 1992-11-04 | 1994-05-05 | Henkel Kgaa | Wäßriges Tensidkonzentrat |
| EP0616028A1 (en) | 1993-03-19 | 1994-09-21 | The Procter & Gamble Company | Cleaning compositions with short chain nonionic surfactants |
| GB9305598D0 (en) | 1993-03-18 | 1993-05-05 | Unilever Plc | Bleach catalyst composition |
| EP0616026A1 (en) | 1993-03-19 | 1994-09-21 | The Procter & Gamble Company | Concentrated cleaning compositions |
| NZ260144A (en) | 1993-04-12 | 1995-10-26 | Colgate Palmolive Co | Cleaning composition; contains three liquid phases which merge at a tricritical point; use for removing tar or grease from articles |
| GB9308047D0 (en) | 1993-04-19 | 1993-06-02 | Unilever Plc | Particulate detergent,bleaching or cleaning compositions containing aluminosilicates |
| DE4313909A1 (de) | 1993-04-28 | 1994-11-03 | Huels Chemische Werke Ag | Wasserenthärtende Formulierungen |
| US5340495A (en) | 1993-04-30 | 1994-08-23 | Siebert, Inc. | Compositions for cleaning ink from a printing press and methods thereof |
| DE4325237A1 (de) | 1993-07-28 | 1995-02-02 | Basf Ag | Verfahren zur Herstellung von Alkoxylierungsprodukten in Gegenwart von mit Additiven modifizierten Mischhydroxiden |
| US5360569A (en) | 1993-11-12 | 1994-11-01 | Lever Brothers Company, Division Of Conopco, Inc. | Activation of bleach precursors with catalytic imine quaternary salts |
| DE4339713A1 (de) | 1993-11-22 | 1995-05-24 | Basf Ag | Verfahren zur Oligomerisierung von Olefinen zu hochlinearen Oligomeren und Katalysatoren dafür |
| ES2119405T3 (es) | 1994-03-31 | 1998-10-01 | Unilever Nv | Composiciones de detergentes. |
| DE4415623A1 (de) | 1994-05-04 | 1995-11-09 | Basf Ag | Verwendung von Pfropfpolymerisaten von monoethylenisch ungesättigten Dicarbonsäuren auf hydrierten Sacchariden als Zusatz zu Wasch- und Reinigungsmitteln |
| DE4416303A1 (de) | 1994-05-09 | 1995-11-16 | Bayer Ag | Schaumarmes Netzmittel und seine Verwendung |
| US5770567A (en) | 1994-11-14 | 1998-06-23 | Genentech, Inc. | Sensory and motor neuron derived factor (SMDF) |
| EG22088A (en) * | 1996-04-16 | 2002-07-31 | Procter & Gamble | Alkoxylated sulfates |
| EG21623A (en) * | 1996-04-16 | 2001-12-31 | Procter & Gamble | Mid-chain branced surfactants |
| ZA974226B (en) * | 1996-05-17 | 1998-12-28 | Procter & Gamble | Detergent composition |
| BR9713144B1 (pt) | 1996-11-26 | 2009-01-13 | composiÇço de Álcool primÁrio ramificado, processo para preparar a mesma, Álcool primÁrio ramificado, composiÇço alcoxilada de Ácool primÁrio ramificado, sulfato de alquila primÁria, carboxilato de alquila primÁria ramificada, e, composiÇço detergente. | |
| HUP0004499A3 (en) * | 1997-10-14 | 2001-12-28 | Procter & Gamble | Granular detergent composition comprising mid-chain branched surfactants |
| ES2237848T3 (es) * | 1997-10-14 | 2005-08-01 | THE PROCTER & GAMBLE COMPANY | Composiciones detergentes para lavar la vajilla, liquidas o en forma de gel, de accion suave que comprenden tensioactivos ramificados a mitad de cadena. |
| DE19912418A1 (de) * | 1999-03-19 | 2000-09-21 | Basf Ag | Verfahren zur Herstellung von Tensidalkoholen und Tensidalkoholethern, die hergestellten Produkte und ihre Verwendung |
| DE19952383A1 (de) | 1999-10-30 | 2001-05-17 | Henkel Kgaa | Wasch- und Reinigungsmittel |
| DE19957173A1 (de) | 1999-11-27 | 2001-05-31 | Basf Ag | Oligomerisierungskatalysator, Verfahren zu seiner Herstellung und seine Verwendung |
| DE10017197A1 (de) * | 2000-04-07 | 2001-10-11 | Basf Ag | Alkoholalkoxylate als schaumarme oder schaumdämpfende Tenside |
| JP4208462B2 (ja) * | 2000-12-28 | 2009-01-14 | 株式会社Ａｄｅｋａ | 界面活性剤 |
| US6515031B2 (en) * | 2001-02-13 | 2003-02-04 | Platte Chemical Company | Technique for emulsifying highly saturated hydroisomerized fluids |
| DE10116021A1 (de) * | 2001-03-30 | 2002-10-24 | Henkel Kgaa | Wasch-oder Reinigungsmittel mit verbesserter Reinigungsleistung |
| DE10218752A1 (de) | 2002-04-26 | 2003-11-13 | Basf Ag | Alkoxylatgemische und diese enthaltende Waschmittel |
| DE10243361A1 (de) | 2002-09-18 | 2004-04-01 | Basf Ag | Alkoxylatgemische und diese enthaltende Waschmittel |
| ES2342464T3 (es) | 2002-04-26 | 2010-07-07 | Basf Se | Mezclas de alcoxilatos de alcanol c sb 10 /sb y su aplicacion. |
| JP2003336092A (ja) | 2002-05-20 | 2003-11-28 | Dai Ichi Kogyo Seiyaku Co Ltd | 濃縮型液体洗浄剤組成物 |
| JP2004035755A (ja) | 2002-07-04 | 2004-02-05 | Sanyo Chem Ind Ltd | ノニオン界面活性剤 |
| DE10310483A1 (de) | 2003-03-11 | 2004-09-23 | Basf Ag | Verfahren zur Herstellung von Oligomeren von Alkenen mit 4 bis 8 Kohlenstoffatomen |
| AU2005219405B2 (en) * | 2004-03-02 | 2007-10-11 | Shell Internationale Research Maatschappij B.V. | Personal care composition comprising highly branched primary alcohol component |
| EP1988986B1 (de) | 2006-02-22 | 2009-12-02 | Basf Se | Tensidgemisch enthaltend kurzkettige sowie langkettige komponenten |
| US7671004B2 (en) * | 2007-02-01 | 2010-03-02 | Basf Aktiengeselschaft | Cleaning composition and method of forming the same |
| CA2619182C (en) * | 2007-02-01 | 2011-06-14 | Basf Corporation | Cleaning composition |
| CA2719153C (en) * | 2008-04-10 | 2016-06-21 | Basf Se | Novel surfactants for tertiary mineral oil extraction based on branched alcohols |
-
2009
- 2009-12-09 TW TW098142090A patent/TW201031743A/zh unknown
- 2009-12-17 AR ARP090104960A patent/AR074787A1/es unknown
- 2009-12-18 US US13/140,653 patent/US20110260101A1/en not_active Abandoned
- 2009-12-18 WO PCT/EP2009/067501 patent/WO2010070088A1/de not_active Ceased
- 2009-12-18 JP JP2011541467A patent/JP5575146B2/ja not_active Expired - Fee Related
- 2009-12-18 CN CN200980151253.6A patent/CN102257110B/zh not_active Expired - Fee Related
- 2009-12-18 KR KR1020117015442A patent/KR20110099714A/ko not_active Abandoned
- 2009-12-18 EP EP09797032A patent/EP2379690A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AR074787A1 (es) | 2011-02-09 |
| TW201031743A (en) | 2010-09-01 |
| CN102257110A (zh) | 2011-11-23 |
| WO2010070088A1 (de) | 2010-06-24 |
| JP5575146B2 (ja) | 2014-08-20 |
| CN102257110B (zh) | 2014-03-05 |
| JP2012512925A (ja) | 2012-06-07 |
| EP2379690A1 (de) | 2011-10-26 |
| US20110260101A1 (en) | 2011-10-27 |
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