CN105339476A - 用于工业齿轮油的协同添加剂组合 - Google Patents
用于工业齿轮油的协同添加剂组合 Download PDFInfo
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- CN105339476A CN105339476A CN201480030345.XA CN201480030345A CN105339476A CN 105339476 A CN105339476 A CN 105339476A CN 201480030345 A CN201480030345 A CN 201480030345A CN 105339476 A CN105339476 A CN 105339476A
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- Prior art keywords
- industrial gear
- oil composition
- gear oil
- component
- ester
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
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- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
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- WMYJOZQKDZZHAC-UHFFFAOYSA-H trizinc;dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([S-])=S.[O-]P([O-])([S-])=S WMYJOZQKDZZHAC-UHFFFAOYSA-H 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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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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
-
- 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
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
-
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/68—Esters
- C10M129/76—Esters containing free hydroxy or carboxyl groups
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/16—Amides; Imides
-
- 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
-
- 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
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/10—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/124—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms containing hydroxy groups; Ethers thereof
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/14—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/144—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/287—Partial esters
- C10M2207/289—Partial esters containing free hydroxy groups
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/08—Amides
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
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- C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/12—Partial amides of polycarboxylic acids
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- C—CHEMISTRY; METALLURGY
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
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- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
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- C10M2223/043—Ammonium or amine salts thereof
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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
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- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/049—Phosphite
-
- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/063—Ammonium or amine salts
-
- 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
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
-
- 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
- C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
Abstract
Description
Claims (16)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US201361828718P | 2013-05-30 | 2013-05-30 | |
US61/828,718 | 2013-05-30 | ||
PCT/US2014/039499 WO2014193784A2 (en) | 2013-05-30 | 2014-05-27 | Synergistic additive combination for industrial gear oils |
Publications (1)
Publication Number | Publication Date |
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CN105339476A true CN105339476A (zh) | 2016-02-17 |
Family
ID=51023096
Family Applications (1)
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CN201480030345.XA Pending CN105339476A (zh) | 2013-05-30 | 2014-05-27 | 用于工业齿轮油的协同添加剂组合 |
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US (1) | US20160122683A1 (zh) |
EP (1) | EP3004297A2 (zh) |
JP (1) | JP2016520158A (zh) |
CN (1) | CN105339476A (zh) |
CA (1) | CA2913176A1 (zh) |
SG (1) | SG11201509216PA (zh) |
TW (1) | TW201504422A (zh) |
WO (1) | WO2014193784A2 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107828482A (zh) * | 2017-11-08 | 2018-03-23 | 蚌埠市华鼎机械科技有限公司 | 一种铅锭冷制粒机中齿轮用润滑油 |
CN112368360A (zh) * | 2018-02-12 | 2021-02-12 | 朗盛公司 | 用于润滑剂的耐磨组合物 |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10208267B2 (en) * | 2014-08-06 | 2019-02-19 | The Lubrizol Corporation | Industrial gear lubricant additive package with biodegradable sulfur component |
JP6405217B2 (ja) * | 2014-12-09 | 2018-10-17 | シェルルブリカンツジャパン株式会社 | すべり案内面用潤滑油組成物 |
US20160168504A1 (en) * | 2014-12-10 | 2016-06-16 | Hyundai Motor Company | Low viscosity gear oil composition providing enhanced fuel efficiency |
TWI664283B (zh) * | 2015-08-07 | 2019-07-01 | 美商盧伯利索公司 | 具有生物可降解硫成分的工業齒輪潤滑添加劑套組及操作工業齒輪之方法 |
SG11201911708TA (en) * | 2017-06-20 | 2020-01-30 | Lubrizol Corp | Lubricating composition |
SG11202009251WA (en) * | 2018-03-21 | 2020-10-29 | Lubrizol Corp | NOVEL FLUORINATED POLYACRYLATES ANTIFOAMS IN ULTRA-LOW VISCOSITY (<5 CST) finished fluids |
JP7408344B2 (ja) | 2019-10-23 | 2024-01-05 | シェルルブリカンツジャパン株式会社 | 潤滑油組成物 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102037108A (zh) * | 2008-03-19 | 2011-04-27 | 卢布里佐尔公司 | 润滑传动系统器件的抗磨组合物和方法 |
CN102575186A (zh) * | 2009-08-18 | 2012-07-11 | 卢布里佐尔公司 | 抗磨损组合物及润滑传动装置的方法 |
WO2012112635A1 (en) * | 2011-02-16 | 2012-08-23 | The Lubrizol Corporation | Lubricating composition and method of lubricating driveline device |
CN102753662A (zh) * | 2009-08-18 | 2012-10-24 | 卢布里佐尔公司 | 含抗磨剂的润滑组合物 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4132702A (en) * | 1974-03-27 | 1979-01-02 | Ciba-Geigy Corporation | Phenol esters and amides and polymers stabilized therewith |
US4741848A (en) * | 1986-03-13 | 1988-05-03 | The Lubrizol Corporation | Boron-containing compositions, and lubricants and fuels containing same |
US6103673A (en) * | 1998-09-14 | 2000-08-15 | The Lubrizol Corporation | Compositions containing friction modifiers for continuously variable transmissions |
US7696136B2 (en) * | 2004-03-11 | 2010-04-13 | Crompton Corporation | Lubricant compositions containing hydroxy carboxylic acid and hydroxy polycarboxylic acid esters |
CN101679897A (zh) * | 2007-05-24 | 2010-03-24 | 卢布里佐尔公司 | 用包含无灰、无硫、无磷抗磨剂的润滑剂润滑硅酸铝复合材料表面的方法 |
US20100093573A1 (en) * | 2007-05-24 | 2010-04-15 | The Lubrizol Corporation | Lubricating Composition Containing Sulphur, Phosphorus and Ashfree Antiwear Agent and Amine Containing Friction Modifier |
KR101496484B1 (ko) * | 2007-05-24 | 2015-03-09 | 더루우브리졸코오포레이션 | 하이드록시폴리카르복시산 유도체 및 몰리브덴 화합물을 기반으로 하는 무회분 내마모제를 함유하는 윤활 조성물 |
EP2235147B1 (en) * | 2007-12-12 | 2019-02-20 | The Lubrizol Corporation | Use for improving fuel efficiency of a marine diesel engine |
WO2010053893A1 (en) * | 2008-11-05 | 2010-05-14 | The Lubrizol Corporation | Method of lubricating an internal combustion engine |
WO2010077538A1 (en) * | 2008-12-09 | 2010-07-08 | The Lubrizol Corporation | Method of operating an engine using an ashless consumable lubricant |
CN102307976A (zh) * | 2008-12-09 | 2012-01-04 | 卢布里佐尔公司 | 含衍生自羟基羧酸的化合物的润滑组合物 |
CA2752682A1 (en) * | 2009-02-18 | 2010-08-26 | The Lubrizol Corporation | Composition containing ester compounds and a method of lubricating an internal combustion engine |
JP5480259B2 (ja) * | 2009-03-10 | 2014-04-23 | ザ ルブリゾル コーポレイション | 動力伝達系路デバイスを潤滑する、耐摩耗組成物および方法 |
US20130324448A1 (en) * | 2012-05-08 | 2013-12-05 | The Lubrizol Corporation | Antiwear Composition and Method of Lubricating Driveline Device |
EP2507349B1 (en) * | 2009-11-30 | 2020-06-10 | The Lubrizol Corporation | Stabilized blends containing friction modifiers |
CA2782216A1 (en) * | 2009-11-30 | 2011-06-03 | The Lubrizol Corporation | Stabilized blends containing friction modifiers |
CN104830407A (zh) * | 2010-08-31 | 2015-08-12 | 路博润公司 | 含有抗磨剂的润滑组合物 |
US8541282B2 (en) * | 2011-11-07 | 2013-09-24 | Intermolecular, Inc. | Blocking layers for leakage current reduction in DRAM devices |
KR101459828B1 (ko) * | 2012-08-07 | 2014-11-10 | 현대자동차주식회사 | 배터리 셀 모듈용 다기능 방열 플레이트 및 이를 갖는 배터리 셀 모듈 |
SG11201501470SA (en) * | 2012-09-11 | 2015-03-30 | Lubrizol Corp | Quaternary ammonium salt containing compositions that provide balanced deposit control and wear performance without seal compatibility issues |
-
2014
- 2014-05-27 EP EP14733832.1A patent/EP3004297A2/en not_active Withdrawn
- 2014-05-27 WO PCT/US2014/039499 patent/WO2014193784A2/en active Application Filing
- 2014-05-27 CA CA2913176A patent/CA2913176A1/en not_active Abandoned
- 2014-05-27 US US14/893,543 patent/US20160122683A1/en not_active Abandoned
- 2014-05-27 SG SG11201509216PA patent/SG11201509216PA/en unknown
- 2014-05-27 JP JP2016516715A patent/JP2016520158A/ja active Pending
- 2014-05-27 CN CN201480030345.XA patent/CN105339476A/zh active Pending
- 2014-05-29 TW TW103118767A patent/TW201504422A/zh unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102037108A (zh) * | 2008-03-19 | 2011-04-27 | 卢布里佐尔公司 | 润滑传动系统器件的抗磨组合物和方法 |
CN102575186A (zh) * | 2009-08-18 | 2012-07-11 | 卢布里佐尔公司 | 抗磨损组合物及润滑传动装置的方法 |
CN102753662A (zh) * | 2009-08-18 | 2012-10-24 | 卢布里佐尔公司 | 含抗磨剂的润滑组合物 |
WO2012112635A1 (en) * | 2011-02-16 | 2012-08-23 | The Lubrizol Corporation | Lubricating composition and method of lubricating driveline device |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107828482A (zh) * | 2017-11-08 | 2018-03-23 | 蚌埠市华鼎机械科技有限公司 | 一种铅锭冷制粒机中齿轮用润滑油 |
CN112368360A (zh) * | 2018-02-12 | 2021-02-12 | 朗盛公司 | 用于润滑剂的耐磨组合物 |
CN112368360B (zh) * | 2018-02-12 | 2022-09-06 | 朗盛公司 | 用于润滑剂的耐磨组合物 |
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US20160122683A1 (en) | 2016-05-05 |
EP3004297A2 (en) | 2016-04-13 |
WO2014193784A3 (en) | 2015-02-26 |
WO2014193784A2 (en) | 2014-12-04 |
TW201504422A (zh) | 2015-02-01 |
SG11201509216PA (en) | 2015-12-30 |
JP2016520158A (ja) | 2016-07-11 |
CA2913176A1 (en) | 2014-12-04 |
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