KR101679090B1 - 블록 공중합체를 함유하는 조성물 및 내연기관을 윤활처리하는 방법 - Google Patents
블록 공중합체를 함유하는 조성물 및 내연기관을 윤활처리하는 방법 Download PDFInfo
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- KR101679090B1 KR101679090B1 KR1020117012684A KR20117012684A KR101679090B1 KR 101679090 B1 KR101679090 B1 KR 101679090B1 KR 1020117012684 A KR1020117012684 A KR 1020117012684A KR 20117012684 A KR20117012684 A KR 20117012684A KR 101679090 B1 KR101679090 B1 KR 101679090B1
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- acrylate
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- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 1
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- 150000003626 triacylglycerols Chemical class 0.000 description 1
- VQOXUMQBYILCKR-UHFFFAOYSA-N tridecaene Natural products CCCCCCCCCCCC=C VQOXUMQBYILCKR-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 238000009736 wetting Methods 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate
- C10M145/12—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate monocarboxylic
- C10M145/14—Acrylate; Methacrylate
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M149/04—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/04—Fatty oil fractions
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- C10M103/00—Lubricating compositions characterised by the base-material being an inorganic material
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/02—Well-defined hydrocarbons
- C10M105/04—Well-defined hydrocarbons aliphatic
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/02—Well-defined hydrocarbons
- C10M105/06—Well-defined hydrocarbons aromatic
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- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/10—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M105/14—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms polyhydroxy
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/22—Carboxylic acids or their salts
- C10M105/24—Carboxylic acids or their salts having only one carboxyl group bound to an acyclic carbon atom, cycloaliphatic carbon atom or hydrogen
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M149/00—Lubricating compositions characterised by the additive being a macromolecular compound containing nitrogen
- C10M149/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M149/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M151/00—Lubricating compositions characterised by the additive being a macromolecular compound containing sulfur, selenium or tellurium
- C10M151/02—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M153/00—Lubricating compositions characterised by the additive being a macromolecular compound containing phosphorus
- C10M153/02—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/022—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/024—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amido or imido group
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/26—Waterproofing or water resistance
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol-fuelled engines
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Engineering & Computer Science (AREA)
- Lubricants (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
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| US11140808P | 2008-11-05 | 2008-11-05 | |
| US61/111,408 | 2008-11-05 | ||
| PCT/US2009/063046 WO2010053890A1 (en) | 2008-11-05 | 2009-11-03 | Composition containing a block copolymer and a method of lubricating an internal combustion engine |
Publications (2)
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| KR20110095286A KR20110095286A (ko) | 2011-08-24 |
| KR101679090B1 true KR101679090B1 (ko) | 2016-11-23 |
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Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP5630923B2 (ja) * | 2009-06-04 | 2014-11-26 | ザ ルブリゾル コーポレイションＴｈｅ Ｌｕｂｒｉｚｏｌ Ｃｏｒｐｏｒａｔｉｏｎ | 摩擦調整剤および粘度調整剤を含む潤滑組成物 |
| KR101758402B1 (ko) * | 2009-09-14 | 2017-07-26 | 더루우브리졸코오포레이션 | 수혼화성이 양호한 농장 트랙터 윤활 조성물 |
| KR20130108597A (ko) * | 2010-10-14 | 2013-10-04 | 에보니크 오일 아디티페스 게엠베하 | 특성을 개선시킨 모터 |
| US20130340325A1 (en) * | 2012-06-22 | 2013-12-26 | Baker Hughes Incorporated | Charged Block Co-polymers as Pour Point Depressants |
| GB201217313D0 (en) * | 2012-09-27 | 2012-11-14 | Univ Sheffield | Block copolymer synthesis |
| JP6072605B2 (ja) * | 2013-05-17 | 2017-02-01 | 昭和シェル石油株式会社 | 内燃機関用潤滑油組成物 |
| JP6606500B2 (ja) * | 2013-09-17 | 2019-11-13 | ヴァンダービルト ケミカルズ、エルエルシー | Ｅ８５燃料を燃料とするエンジンに適したエマルション組成物における水の分離を低減する方法 |
| US9879201B2 (en) * | 2014-02-28 | 2018-01-30 | Cosmo Oil Lubricants Co., Ltd. | Engine oil composition |
| RU2692794C2 (ru) * | 2014-06-19 | 2019-06-27 | Шелл Интернэшнл Рисерч Маатсхаппий Б.В. | Смазывающая композиция |
| JP6324240B2 (ja) * | 2014-07-04 | 2018-05-16 | 第一工業製薬株式会社 | 粘度指数向上剤およびこれを含有する潤滑油組成物 |
| JP5866700B1 (ja) * | 2015-05-12 | 2016-02-17 | 国立大学法人東北大学 | 潤滑油添加剤および潤滑油組成物 |
| US9765487B2 (en) | 2015-09-08 | 2017-09-19 | Baldwin Paving Co., Inc. | Systems for applying roadway surface treatments, and methods of using same |
| FR3041349B1 (fr) * | 2015-09-18 | 2020-01-24 | Total Marketing Services | Copolymere utilisable comme additif detergent pour carburant |
| EP3257920A1 (en) * | 2016-06-17 | 2017-12-20 | Total Marketing Services | Lubricant polymers |
| EP3257919B1 (en) | 2016-06-17 | 2020-08-19 | Total Marketing Services | Lubricant polymers |
| JP6813996B2 (ja) * | 2016-08-31 | 2021-01-13 | 大塚化学株式会社 | ブロック共重合体、および、これを含有する樹脂改質剤、エポキシ樹脂組成物 |
| BR112019005332A2 (pt) | 2016-09-21 | 2019-06-11 | Lubrizol Corp | componentes antiespumantes de poliacrilato para uso em combustíveis de diesel |
| WO2018069460A1 (en) * | 2016-10-12 | 2018-04-19 | Chevron Oronite Technology B.V. | Marine diesel lubricant oil compositions |
| CA3066524A1 (en) | 2017-06-27 | 2019-01-03 | The Lubrizol Corporation | Lubricating composition for and method of lubricating an internal combustion engine |
| EP3770235B1 (en) * | 2018-09-24 | 2022-06-29 | Infineum International Limited | Polymers and lubricating compositions containing polymers |
| EP3898907B1 (en) | 2018-12-19 | 2025-02-05 | Evonik Operations GmbH | Use of associative triblockcopolymers as viscosity index improvers |
| US11680222B2 (en) * | 2020-10-30 | 2023-06-20 | Afton Chemical Corporation | Engine oils with low temperature pumpability |
| IL303390A (en) | 2020-12-03 | 2023-08-01 | Battelle Memorial Institute | Compositions of polymer nanoparticles and DNA nanostructures and methods for non-viral transport |
| WO2022216977A1 (en) | 2021-04-07 | 2022-10-13 | Batelle Memorial Institute | Rapid design, build, test, and learn technologies for identifying and using non-viral carriers |
| CN113862064A (zh) * | 2021-10-13 | 2021-12-31 | 中国石油化工股份有限公司 | 一种发动机油组合物 |
| US12515668B2 (en) * | 2023-02-20 | 2026-01-06 | Honda Motor Co., Ltd. | Systems and methods for vehicular navigation at traffic signals |
| CN121773146A (zh) * | 2023-08-11 | 2026-03-31 | 科凝生物医药科技(杭州)有限公司 | 嵌段式共聚物的润滑组合物及其用途 |
| WO2025072751A1 (en) | 2023-09-29 | 2025-04-03 | Battelle Memorial Institute | Polymer nanoparticle compositions for in vivo expression of polypeptides |
| AU2024393766A1 (en) | 2023-12-08 | 2026-06-18 | Battelle Memorial Institute | Use of dna origami nanostructures for molecular information based data storage systems |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060189490A1 (en) * | 2003-03-31 | 2006-08-24 | Alexander Dardin | Lubricating oil composition with good frictional properties |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3816314A (en) * | 1972-05-31 | 1974-06-11 | Exxon Research Engineering Co | Block copolymers of unsaturated ester and a nitrogen containing monomer as v.i.improving and dispersant additives for oils |
| EP0265254A3 (en) * | 1986-10-23 | 1990-03-21 | E.I. Du Pont De Nemours And Company | Oil additives |
| US4985160A (en) * | 1989-02-08 | 1991-01-15 | E. I. Du Pont De Nemours And Company | Branched polymers as fuel oil additives |
| US4941984A (en) * | 1989-07-31 | 1990-07-17 | The Lubrizol Corporation | Lubricating oil compositions and methods for lubricating gasoline-fueled and/or alcohol-fueled, spark-ignited engines |
| DE19603696A1 (de) * | 1996-02-02 | 1997-08-07 | Roehm Gmbh | Demulgatoren |
| FR2833186B1 (fr) * | 2001-12-12 | 2004-01-23 | Rhodia Chimie Sa | Utilisation de copolymeres cationiques a blocs comme aide au depot d'emulsions simples ou multiples |
| AU2003240594A1 (en) * | 2002-05-03 | 2003-11-17 | Basf Aktiengesellschaft | Cosmetic product comprising at least one water-soluble copolymer which contains (meth)acrylamide units |
| WO2005056739A1 (en) * | 2003-11-26 | 2005-06-23 | Arkema Inc. | Controlled radical acrylic copolymer thickeners |
| JP2007238663A (ja) * | 2006-03-06 | 2007-09-20 | Sanyo Chem Ind Ltd | 潤滑油添加剤および潤滑油組成物 |
| DE102005015931A1 (de) * | 2005-04-06 | 2006-10-12 | Rohmax Additives Gmbh | Polyalkyl(meth) acrylat-Copolymere mit hervorragenden Eigenschaften |
| JP5106778B2 (ja) * | 2006-01-24 | 2012-12-26 | 三洋化成工業株式会社 | 潤滑油用スラッジ分散剤 |
| EP2039745B1 (en) * | 2006-03-15 | 2013-06-05 | Nippon Oil Corporation | Lube base oil, lubricating oil composition for internal combustion engine, and lubricating oil composition for drive transmission device |
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2009
- 2009-11-03 BR BRPI0921231A patent/BRPI0921231A2/pt not_active Application Discontinuation
- 2009-11-03 EP EP09748200A patent/EP2358849A1/en not_active Withdrawn
- 2009-11-03 CN CN2009801534821A patent/CN102272278A/zh active Pending
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- 2009-11-03 CA CA2742516A patent/CA2742516C/en active Active
- 2009-11-03 WO PCT/US2009/063046 patent/WO2010053890A1/en not_active Ceased
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2016
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2017
- 2017-10-12 US US15/730,879 patent/US20180030366A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060189490A1 (en) * | 2003-03-31 | 2006-08-24 | Alexander Dardin | Lubricating oil composition with good frictional properties |
Also Published As
| Publication number | Publication date |
|---|---|
| US20160362628A1 (en) | 2016-12-15 |
| CN105296063A (zh) | 2016-02-03 |
| CA2742516A1 (en) | 2010-05-14 |
| AU2009311294A1 (en) | 2010-05-14 |
| KR20110095286A (ko) | 2011-08-24 |
| BRPI0921231A2 (pt) | 2018-06-26 |
| CA2742516C (en) | 2019-06-04 |
| US20180030366A1 (en) | 2018-02-01 |
| AU2016219628A1 (en) | 2016-09-08 |
| EP2358849A1 (en) | 2011-08-24 |
| WO2010053890A1 (en) | 2010-05-14 |
| CN102272278A (zh) | 2011-12-07 |
| JP5559803B2 (ja) | 2014-07-23 |
| JP2012507613A (ja) | 2012-03-29 |
| US20110263470A1 (en) | 2011-10-27 |
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