NO311040B1 - Multifunksjonelle viskositetsmodifiserende midler av blandede etylen-alfaolefinkopolymerer som er nyttige ismoreoljesammensetninger - Google Patents
Multifunksjonelle viskositetsmodifiserende midler av blandede etylen-alfaolefinkopolymerer som er nyttige ismoreoljesammensetninger Download PDFInfo
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- NO311040B1 NO311040B1 NO19952268A NO952268A NO311040B1 NO 311040 B1 NO311040 B1 NO 311040B1 NO 19952268 A NO19952268 A NO 19952268A NO 952268 A NO952268 A NO 952268A NO 311040 B1 NO311040 B1 NO 311040B1
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- Prior art keywords
- ethylene
- copolymer
- weight
- derivatized
- oil
- Prior art date
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Classifications
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- C10M161/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
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- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
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- C08F8/48—Isomerisation; Cyclisation
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- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
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- C10M2209/082—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 monocarboxylic
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- C10N2070/00—Specific manufacturing methods for lubricant compositions
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Lubricants (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/989,418 US5427702A (en) | 1992-12-11 | 1992-12-11 | Mixed ethylene alpha olefin copolymer multifunctional viscosity modifiers useful in lube oil compositions |
PCT/US1993/011727 WO1994013763A1 (en) | 1992-12-11 | 1993-12-03 | Mixed ethylene alpha olefin copolymer multifunctional viscosity modifiers useful in lube oil compositions |
Publications (3)
Publication Number | Publication Date |
---|---|
NO952268D0 NO952268D0 (no) | 1995-06-08 |
NO952268L NO952268L (no) | 1995-08-02 |
NO311040B1 true NO311040B1 (no) | 2001-10-01 |
Family
ID=25535097
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19952268A NO311040B1 (no) | 1992-12-11 | 1995-06-08 | Multifunksjonelle viskositetsmodifiserende midler av blandede etylen-alfaolefinkopolymerer som er nyttige ismoreoljesammensetninger |
Country Status (23)
Country | Link |
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US (2) | US5427702A (de) |
EP (1) | EP0673407B1 (de) |
JP (1) | JP3616092B2 (de) |
KR (1) | KR100201219B1 (de) |
CN (1) | CN1033519C (de) |
AT (1) | ATE171981T1 (de) |
AU (1) | AU669257B2 (de) |
BR (1) | BR9307616A (de) |
CA (1) | CA2150801C (de) |
CZ (1) | CZ137195A3 (de) |
DE (2) | DE69321485D1 (de) |
ES (1) | ES2124868T3 (de) |
FI (1) | FI952849A (de) |
HU (1) | HU214353B (de) |
MX (1) | MX9307766A (de) |
NO (1) | NO311040B1 (de) |
PL (1) | PL175423B1 (de) |
RU (1) | RU2103333C1 (de) |
SG (1) | SG52636A1 (de) |
SK (1) | SK281774B6 (de) |
TW (1) | TW316269B (de) |
UA (1) | UA46703C2 (de) |
WO (1) | WO1994013763A1 (de) |
Families Citing this family (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5427702A (en) * | 1992-12-11 | 1995-06-27 | Exxon Chemical Patents Inc. | Mixed ethylene alpha olefin copolymer multifunctional viscosity modifiers useful in lube oil compositions |
US6255387B1 (en) * | 1993-08-02 | 2001-07-03 | Ethyl Additives Corporation | Derivatized solid sheared polymer blends and process for their preparation |
CA2127918A1 (en) * | 1993-08-02 | 1995-02-03 | Maria Magdalena Kapuscinski | Dimensionally stable solid polymer blend and a lubricating oil composition containing same |
US5663126A (en) | 1994-10-21 | 1997-09-02 | Castrol Limited | Polar grafted polyolefins, methods for their manufacture, and lubricating oil compositions containing them |
US5639718A (en) | 1994-11-23 | 1997-06-17 | Exxon Chemical Patents Inc. | Multifunctional viscosity modifiers for lubricating oil compositions with improved dispersancy and antioxidancy derived from adducts of quinone |
GB9511267D0 (en) * | 1995-06-05 | 1995-08-02 | Exxon Chemical Patents Inc | Lubricating oils comprising low saturate basestock |
GB9519668D0 (en) † | 1995-09-27 | 1995-11-29 | Exxon Chemical Patents Inc | Low chlorine low ash crankcase lubricant |
US6187721B1 (en) | 1996-06-12 | 2001-02-13 | Castrol Limited | Lubricant for use in diesel engines |
GB9612278D0 (en) * | 1996-06-12 | 1996-08-14 | Castrol Ltd | A lubricant for use in diesel engines |
US6107258A (en) * | 1997-10-15 | 2000-08-22 | Ethyl Corporation | Functionalized olefin copolymer additives |
US5972853A (en) * | 1997-11-12 | 1999-10-26 | Exxon Chemical Patents Inc. | Wear control with dispersants employing poly alpha-olefin polymers |
US6107257A (en) * | 1997-12-09 | 2000-08-22 | Ethyl Corporation | Highly grafted, multi-functional olefin copolymer VI modifiers |
US6025308A (en) * | 1998-09-10 | 2000-02-15 | R. T. Vanderbilt Company, Inc. | Amine-functionalized polymers |
CN1390234A (zh) * | 1999-10-19 | 2003-01-08 | 埃克森化学专利公司 | 含胺基接枝聚合物,其制备方法和它们的用途 |
US6221967B1 (en) | 1999-12-16 | 2001-04-24 | Shell Oil Company | Preformed multi-acid adducts useful for grafting polyolefin polymers |
US6448333B1 (en) | 1999-12-16 | 2002-09-10 | Shell Oil Company | Polyfunctional polyolefins |
US6271306B1 (en) | 1999-12-16 | 2001-08-07 | Shell Oil Company | Water based adhesive emulsions based on multi-acid functionalized polyolefins |
US6475963B1 (en) * | 2001-05-01 | 2002-11-05 | Infineum International Ltd. | Carboxylate-vinyl ester copolymer blend compositions for lubricating oil flow improvement |
EP1513794B1 (de) * | 2002-05-24 | 2013-03-06 | Castrol Limited | Herstellung von monomeren zum aufpfropfen auf polyolefine, und schmierölzusammensetzungen, die das pfropfcopolymer enthalten |
US7285583B2 (en) * | 2002-07-30 | 2007-10-23 | Liquamelt Licensing Llc | Hybrid plastisol/hot melt compositions |
US7514393B2 (en) * | 2003-11-21 | 2009-04-07 | Castrol Limited | Preparation of functional monomers for grafting to low molecular weight polyalkenes and their use in the preparation of dispersants and lubricating oil compositions containing dispersant polyalkenes |
US7207308B2 (en) * | 2004-05-21 | 2007-04-24 | Afton Chemical Corporation | Filterless crankcase lubrication system for a vehicle |
US20060003905A1 (en) * | 2004-07-02 | 2006-01-05 | Devlin Cathy C | Additives and lubricant formulations for improved corrosion protection |
JP5070049B2 (ja) * | 2004-07-30 | 2012-11-07 | ザ ルブリゾル コーポレイション | 芳香族アミンを含有する分散剤粘度調整剤 |
US7700684B2 (en) | 2004-12-09 | 2010-04-20 | Afton Chemical Corporation | Graft functionalized olefin polymer dispersant and uses thereof |
US7253231B2 (en) * | 2005-01-31 | 2007-08-07 | Afton Chemical Corporation | Grafted multi-functional olefin copolymer VI modifiers and uses thereof |
US8703872B2 (en) * | 2005-03-11 | 2014-04-22 | Castrol Limited | Multiple function graft polymer |
WO2006116663A1 (en) | 2005-04-28 | 2006-11-02 | Castrol Limited | Multiple-function dispersant graft polymer |
US7745542B2 (en) * | 2005-04-29 | 2010-06-29 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US7745541B2 (en) * | 2005-04-29 | 2010-06-29 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US8338343B2 (en) * | 2005-06-13 | 2012-12-25 | Lanxess Elastomers B.V. | Additive composition comprising an amidized or imidized polymer |
US7399737B2 (en) * | 2005-06-13 | 2008-07-15 | Exxonmobil Chemical Patents Inc. | Lube additives |
US20070004604A1 (en) * | 2005-07-01 | 2007-01-04 | Mathur Naresh C | Additive composition |
US7618928B2 (en) | 2005-08-31 | 2009-11-17 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US20070149414A1 (en) * | 2005-12-28 | 2007-06-28 | Chevron Oronite Company Llc | Dispersant viscosity index improvers having high ethylene content and lubricating oil compositions containing the same |
US8124225B2 (en) * | 2006-07-18 | 2012-02-28 | Omnova Solutions Inc. | Aqueous floor polishing composition |
US7928044B2 (en) | 2006-10-27 | 2011-04-19 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US7816309B2 (en) * | 2006-10-27 | 2010-10-19 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US7820604B2 (en) * | 2006-10-27 | 2010-10-26 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US8067347B2 (en) * | 2006-10-27 | 2011-11-29 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US7858566B2 (en) | 2006-10-27 | 2010-12-28 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
US7820605B2 (en) * | 2006-10-27 | 2010-10-26 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
TWI488873B (zh) * | 2006-12-21 | 2015-06-21 | Dow Global Technologies Llc | 官能化的烯烴聚合物,由其製備之組成物及物件,及其之製造方法(二) |
US9200103B2 (en) | 2006-12-21 | 2015-12-01 | Dow Global Technologies Llc | Functionalized olefin polymers, compositions and articles prepared therefrom, and methods for making the same |
US8981013B2 (en) * | 2006-12-21 | 2015-03-17 | Dow Global Technologies Llc | Functionalized olefin polymers, compositions and articles prepared therefrom, and methods for making the same |
US8455568B2 (en) * | 2008-04-25 | 2013-06-04 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
CN104277144A (zh) | 2008-07-31 | 2015-01-14 | 卢布里佐尔公司 | 共聚物及其润滑组合物 |
US8378042B2 (en) * | 2009-04-28 | 2013-02-19 | Exxonmobil Chemical Patents Inc. | Finishing process for amorphous polymers |
US9127151B2 (en) | 2009-04-28 | 2015-09-08 | Exxonmobil Chemical Patents Inc. | Polymer compositions having improved properties as viscosity index improvers and use thereof in lubricating oils |
JP5575892B2 (ja) | 2009-07-08 | 2014-08-20 | ザ ルブリゾル コーポレイション | 分散性粘度調整剤 |
KR101789340B1 (ko) | 2009-07-08 | 2017-11-20 | 더루우브리졸코오포레이션 | 점도 조정제로서 유용한 중합체 블렌드 |
KR20120049877A (ko) * | 2009-07-08 | 2012-05-17 | 더루우브리졸코오포레이션 | 분산제 점도 조정제 |
CN102648217B (zh) | 2009-11-17 | 2015-11-25 | 凯斯特罗有限公司 | 多官能多接枝单体的低分子量聚合物 |
WO2011107336A1 (en) | 2010-03-01 | 2011-09-09 | Dsm Ip Assets B.V. | Functionalized olefin copolymer |
WO2011123408A1 (en) | 2010-04-01 | 2011-10-06 | Castrol Limited | Multiple function graft polymer |
CN102844344B (zh) | 2010-04-07 | 2015-08-26 | 凯斯特罗有限公司 | 接枝聚合物及相关方法和组合物 |
WO2011146692A1 (en) | 2010-05-20 | 2011-11-24 | The Lubrizol Corporation | Lubricating composition containing a dispersant |
US8969266B2 (en) | 2010-06-02 | 2015-03-03 | The Lubrizol Corporation | Lubricating composition containing a carboxylic functionalised polymer |
EP2809716B1 (de) * | 2012-02-03 | 2018-01-24 | ExxonMobil Chemical Patents Inc. | Verfahren zur herstellung von polymerzusammensetzungen zur verwendung als ölmodifikatoren |
WO2013123160A1 (en) | 2012-02-17 | 2013-08-22 | The Lubrizol Corporation | Mixtures of olefin-ester copolymer with polyolefin as viscosity modifier |
CA2864431A1 (en) | 2012-02-17 | 2013-08-22 | The Lubrizol Corporation | Lubricating composition including esterified copolymer and low dispersant levels suitable for driveline applications |
US9115237B2 (en) | 2012-07-18 | 2015-08-25 | Chevron Oronite Company Llc | Viscosity improver grafted with unsaturated acylating agent and an aryloxyalylkene monoamine |
EP2898051B1 (de) | 2012-09-24 | 2017-08-16 | The Lubrizol Corporation | Schmierstoff enthaltend eine mischung aus einem olefin-ester copolymer und einem ethylene alpha-olefin copolymer |
US9624451B2 (en) | 2013-03-15 | 2017-04-18 | Castrol Limited | Multiple function dispersant viscosity index improver |
EP3058029B1 (de) * | 2013-10-16 | 2017-11-22 | E. I. du Pont de Nemours and Company | Doppelkomponentensystem zur polyolefinkompatibilisierung |
WO2015088769A2 (en) | 2013-12-10 | 2015-06-18 | The Lubrizol Corporation | Method for preparing functionalized graft polymers |
EP3092289B1 (de) | 2014-01-10 | 2020-08-12 | The Lubrizol Corporation | Methode zum schmieren eines verbrennungsmotors |
US20160326453A1 (en) | 2014-01-10 | 2016-11-10 | The Lubrizol Corporation | Method of lubricating an internal combustion engine |
US20170073606A1 (en) | 2014-03-12 | 2017-03-16 | The Lubrizol Corporation | Method of lubricating an internal combustion engine |
EP3268456A1 (de) | 2015-03-09 | 2018-01-17 | The Lubrizol Corporation | Verfahren zum schmieren eines verbrennungsmotors |
EP3405554B1 (de) | 2016-01-22 | 2019-12-25 | Chevron Oronite Company LLC | Schmierölzusammensetzung mit einer mischung aus olefincopolymerdispergiermittel als viskositätsverbesserer und aminverbindung |
EP3512926B1 (de) | 2016-09-14 | 2021-02-17 | The Lubrizol Corporation | Schmierstoffzusammensetzung und verfahren zum schmieren eines verbrennungsmotors |
EP4345114A3 (de) * | 2016-09-28 | 2024-07-10 | Dow Global Technologies Llc | Schmiermittelbehandlungen für radikalische polymerisationen |
EP3645682B1 (de) | 2017-06-27 | 2022-08-03 | The Lubrizol Corporation | Schmiermittelzusammensetzung mit einem selbstanordnenden polymethacrylat-blockcopolymer und einem ethylen-alpha-olefin-copolymer |
EP3896142A1 (de) | 2017-06-27 | 2021-10-20 | The Lubrizol Corporation | Schmiermittelzusammensetzung und verfahren zum schmieren einer brennkraftmaschine |
CN111032838A (zh) | 2017-07-17 | 2020-04-17 | 路博润公司 | 低分散剂润滑剂组合物 |
US11098262B2 (en) * | 2018-04-25 | 2021-08-24 | Afton Chemical Corporation | Multifunctional branched polymers with improved low-temperature performance |
KR20230066548A (ko) | 2020-09-14 | 2023-05-16 | 에코랍 유에스에이 인코퍼레이티드 | 플라스틱-유도 합성 공급원료를 위한 저온 흐름 첨가제 |
US11505761B2 (en) * | 2020-09-17 | 2022-11-22 | Exxon Mobil Technology and Engineering Company | Diluent oils for viscosity modifiers and additive packages |
US11773343B2 (en) | 2021-11-17 | 2023-10-03 | Afton Chemical Corporation | Engine oil formulation with improved Sequence VIII performance |
US11898119B2 (en) | 2022-01-25 | 2024-02-13 | Afton Chemical Corporation | Lubricating oil compositions with resistance to engine deposit and varnish formation |
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Family Cites Families (48)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3779928A (en) * | 1969-04-01 | 1973-12-18 | Texaco Inc | Automatic transmission fluid |
NL170019C (nl) * | 1970-06-02 | Exxon Research Engineering Co | Werkwijze ter bereiding van een smeeroliemengsel. | |
US3932290A (en) * | 1973-10-04 | 1976-01-13 | The Lubrizol Corporation | Phosphorus-containing friction modifiers for functional fluids |
US3852205A (en) * | 1973-11-05 | 1974-12-03 | Texaco Inc | Transmission fluid compositions and method |
US3879306A (en) * | 1973-11-05 | 1975-04-22 | Texaco Inc | Automatic transmission fluid |
US3933659A (en) * | 1974-07-11 | 1976-01-20 | Chevron Research Company | Extended life functional fluid |
AU498559B2 (en) * | 1975-06-25 | 1979-03-15 | Exxon Research And Engineering Company | Lubricating oil concentrate |
JPS58445B2 (ja) * | 1975-10-17 | 1983-01-06 | 三井化学株式会社 | 熱可塑性エラストマ−の製造方法 |
US4028258A (en) * | 1975-12-03 | 1977-06-07 | Texaco Inc. | Alkylene oxide adducts of phosphosulfurized N-(hydroxyalkyl) alkenylsuccinimides |
US4033889A (en) * | 1976-10-18 | 1977-07-05 | Shell Oil Company | Terpolymer dispersant - VI improver |
US4235731A (en) * | 1976-10-18 | 1980-11-25 | Shell Oil Company | Modified terpolymer dispersant - VI improver |
GB1578049A (en) * | 1976-12-29 | 1980-10-29 | Texaco Development Corp | Succinimide derivatives of a copolymer of ehtylene and propylene |
US4161452A (en) * | 1977-01-28 | 1979-07-17 | Rohm And Haas Company | Polyolefinic copolymer additives for lubricants and fuels |
US4169063A (en) * | 1977-03-11 | 1979-09-25 | Shell Oil Company | EPR dispersant VI improver |
US4105571A (en) * | 1977-08-22 | 1978-08-08 | Exxon Research & Engineering Co. | Lubricant composition |
US4160739A (en) * | 1977-12-05 | 1979-07-10 | Rohm And Haas Company | Polyolefinic copolymer additives for lubricants and fuels |
US4320019A (en) * | 1978-04-17 | 1982-03-16 | The Lubrizol Corporation | Multi-purpose additive compositions and concentrates containing same |
US4357250A (en) * | 1978-04-17 | 1982-11-02 | The Lubrizol Corporation | Nitrogen-containing terpolymer-based compositions useful as multi-purpose lubricant additives |
US4176074A (en) * | 1978-09-18 | 1979-11-27 | Exxon Research & Engineering Co. | Molybdenum complexes of ashless oxazoline dispersants as friction reducing antiwear additives for lubricating oils |
US4344853A (en) * | 1980-10-06 | 1982-08-17 | Exxon Research & Engineering Co. | Functional fluid containing metal salts of esters of hydrocarbyl succinic acid or anhydride with thio-bis-alkanols as antioxidants |
US4505834A (en) * | 1980-10-27 | 1985-03-19 | Edwin Cooper, Inc. | Lubricating oil compositions containing graft copolymer as viscosity index improver-dispersant |
CA1184554A (en) * | 1981-03-23 | 1985-03-26 | Andrew G. Papay | Lubricating oil compositions |
US4517104A (en) * | 1981-05-06 | 1985-05-14 | Exxon Research & Engineering Co. | Ethylene copolymer viscosity index improver-dispersant additive useful in oil compositions |
US4507515A (en) * | 1983-12-21 | 1985-03-26 | Exxon Research & Engineering Co. | Lubricating oil compositions containing ethylene-alpha-olefin polymers of controlled sequence distribution and molecular heterogeneity |
CA1264880A (en) * | 1984-07-06 | 1990-01-23 | John Brooke Gardiner | Viscosity index improver - dispersant additive useful in oil compositions |
US4735736A (en) * | 1985-07-08 | 1988-04-05 | Exxon Chemical Patents Inc. | Viscosity index improver-dispersant additive |
US4863624A (en) * | 1987-09-09 | 1989-09-05 | Exxon Chemical Patents Inc. | Dispersant additives mixtures for oleaginous compositions |
JPS63196690A (ja) * | 1987-02-12 | 1988-08-15 | Mitsui Petrochem Ind Ltd | 潤滑油組成物 |
US4839074A (en) * | 1987-05-22 | 1989-06-13 | Exxon Chemical Patents Inc. | Specified C14 -carboxylate/vinyl ester polymer-containing compositions for lubricating oil flow improvement |
US4803003A (en) * | 1987-06-16 | 1989-02-07 | Exxon Chemical Patents Inc. | Ethylene copolymer viscosity index improver dispersant additive useful in oil compositions |
US5102566A (en) * | 1987-10-02 | 1992-04-07 | Exxon Chemical Patents Inc. | Low ash lubricant compositions for internal combustion engines (pt-727) |
FR2622891B1 (de) * | 1987-11-05 | 1990-02-02 | Elf Aquitaine | |
US4863623A (en) * | 1988-03-24 | 1989-09-05 | Texaco Inc. | Novel VI improver, dispersant, and anti-oxidant additive and lubricating oil composition containing same |
US4921625A (en) * | 1988-06-27 | 1990-05-01 | Shell Oil Company | Method for preparing functionalized block copolymers |
US5035821A (en) * | 1988-07-18 | 1991-07-30 | Exxon Chemical Patents Inc. | End-capped multifunctional viscosity index improver |
FR2640272B1 (fr) * | 1988-12-12 | 1992-07-24 | Elf Aquitaine | Composes polymeriques resultant de la condensation d'une alkylene polyamine sur un copolymere ayant des groupements carboxyliques vicinaux et leur utilisation comme additifs aux lubrifiants |
US5073383A (en) * | 1989-04-21 | 1991-12-17 | Affinity Biotech, Inc. | Inhibiting aggregation in fluorocarbon emulsions |
CA2015061A1 (en) * | 1989-05-30 | 1990-11-30 | Antonio Gutierrez | Multifunctional viscosity index modifier additives derived from polyamines containing one primary amino group and at least one secondary amino group |
US5238588A (en) * | 1989-08-24 | 1993-08-24 | Texaco Inc. | Dispersant, vi improver, additive and lubricating oil composition containing same |
US5068047A (en) * | 1989-10-12 | 1991-11-26 | Exxon Chemical Patents, Inc. | Visosity index improver |
US5073600A (en) * | 1989-10-12 | 1991-12-17 | Shell Oil Company | Dispersant viscosity index improvers |
US5275747A (en) * | 1990-02-01 | 1994-01-04 | Exxon Chemical Patents Inc. | Derivatized ethylene alpha-olefin polymer useful as multifunctional viscosity index improver additive for oleaginous composition |
US5075383A (en) * | 1990-04-11 | 1991-12-24 | Texaco Inc. | Dispersant and antioxidant additive and lubricating oil composition containing same |
US5112508A (en) * | 1990-04-30 | 1992-05-12 | Texaco, Inc. | VI improver, dispersant, and antioxidant additive and lubricating oil composition |
US5139688A (en) * | 1990-08-06 | 1992-08-18 | Texaco, Inc. | Dispersant and antioxidant additive and lubricating oil composition containing same |
US5162086A (en) * | 1991-05-22 | 1992-11-10 | Texaco Inc. | Dispersant additive and lubricating oil composition containing same |
US5160446A (en) * | 1991-05-22 | 1992-11-03 | Texaco Inc. | Dispersant, vi improver and antioxidant additive, and lubricating oil composition containing same |
US5427702A (en) * | 1992-12-11 | 1995-06-27 | Exxon Chemical Patents Inc. | Mixed ethylene alpha olefin copolymer multifunctional viscosity modifiers useful in lube oil compositions |
-
1992
- 1992-12-11 US US07/989,418 patent/US5427702A/en not_active Expired - Lifetime
-
1993
- 1993-12-03 BR BR9307616A patent/BR9307616A/pt not_active IP Right Cessation
- 1993-12-03 PL PL93309343A patent/PL175423B1/pl unknown
- 1993-12-03 AT AT94903420T patent/ATE171981T1/de not_active IP Right Cessation
- 1993-12-03 AU AU57376/94A patent/AU669257B2/en not_active Ceased
- 1993-12-03 JP JP51426294A patent/JP3616092B2/ja not_active Expired - Lifetime
- 1993-12-03 CA CA002150801A patent/CA2150801C/en not_active Expired - Lifetime
- 1993-12-03 SK SK679-95A patent/SK281774B6/sk unknown
- 1993-12-03 EP EP94903420A patent/EP0673407B1/de not_active Expired - Lifetime
- 1993-12-03 DE DE69321485A patent/DE69321485D1/de not_active Expired - Lifetime
- 1993-12-03 ES ES94903420T patent/ES2124868T3/es not_active Expired - Lifetime
- 1993-12-03 UA UA95073138A patent/UA46703C2/uk unknown
- 1993-12-03 RU RU95121940/04A patent/RU2103333C1/ru not_active IP Right Cessation
- 1993-12-03 CZ CZ951371A patent/CZ137195A3/cs unknown
- 1993-12-03 WO PCT/US1993/011727 patent/WO1994013763A1/en not_active Application Discontinuation
- 1993-12-03 HU HU9501684A patent/HU214353B/hu not_active IP Right Cessation
- 1993-12-03 KR KR1019950702117A patent/KR100201219B1/ko not_active IP Right Cessation
- 1993-12-03 DE DE69321485T patent/DE69321485T4/de not_active Expired - Lifetime
- 1993-12-03 SG SG1996007193A patent/SG52636A1/en unknown
- 1993-12-08 MX MX9307766A patent/MX9307766A/es not_active IP Right Cessation
- 1993-12-10 CN CN93120879A patent/CN1033519C/zh not_active Expired - Lifetime
-
1994
- 1994-01-13 TW TW082110442A patent/TW316269B/zh active
-
1995
- 1995-06-08 NO NO19952268A patent/NO311040B1/no unknown
- 1995-06-09 FI FI952849A patent/FI952849A/fi unknown
-
1996
- 1996-06-27 US US08/671,563 patent/US5744429A/en not_active Expired - Lifetime
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