JP2008111122A5 - - Google Patents
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- Publication number
- JP2008111122A5 JP2008111122A5 JP2007277358A JP2007277358A JP2008111122A5 JP 2008111122 A5 JP2008111122 A5 JP 2008111122A5 JP 2007277358 A JP2007277358 A JP 2007277358A JP 2007277358 A JP2007277358 A JP 2007277358A JP 2008111122 A5 JP2008111122 A5 JP 2008111122A5
- Authority
- JP
- Japan
- Prior art keywords
- copolymer
- lubricating oil
- carbon atoms
- group
- composition according
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims 71
- 229920001577 copolymer Polymers 0.000 claims 70
- 239000010687 lubricating oil Substances 0.000 claims 61
- 125000004432 carbon atom Chemical group C* 0.000 claims 56
- 125000000217 alkyl group Chemical group 0.000 claims 41
- 239000000654 additive Substances 0.000 claims 37
- 230000000996 additive effect Effects 0.000 claims 37
- 150000001875 compounds Chemical class 0.000 claims 30
- 229910052739 hydrogen Inorganic materials 0.000 claims 28
- 239000001257 hydrogen Substances 0.000 claims 28
- 125000003342 alkenyl group Chemical group 0.000 claims 25
- 150000002431 hydrogen Chemical class 0.000 claims 25
- -1 monoolefin compound Chemical class 0.000 claims 21
- 125000003545 alkoxy group Chemical group 0.000 claims 20
- 150000002148 esters Chemical class 0.000 claims 20
- 239000004721 Polyphenylene oxide Substances 0.000 claims 18
- 229920000570 polyether Polymers 0.000 claims 18
- 125000002877 alkyl aryl group Chemical group 0.000 claims 17
- 125000003710 aryl alkyl group Chemical group 0.000 claims 17
- 239000003921 oil Substances 0.000 claims 14
- 150000001491 aromatic compounds Chemical class 0.000 claims 13
- 229920000768 polyamine Polymers 0.000 claims 12
- 125000003118 aryl group Chemical group 0.000 claims 11
- 238000006555 catalytic reaction Methods 0.000 claims 11
- 150000008064 anhydrides Chemical class 0.000 claims 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 8
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 claims 6
- 150000001336 alkenes Chemical class 0.000 claims 6
- 229950003476 aminothiazole Drugs 0.000 claims 6
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims 6
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims 6
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 6
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 6
- 229920002554 vinyl polymer Polymers 0.000 claims 6
- MNLAVFKVRUQAKW-UHFFFAOYSA-N VR nerve agent Chemical compound CCN(CC)CCSP(C)(=O)OCC(C)C MNLAVFKVRUQAKW-UHFFFAOYSA-N 0.000 claims 5
- 125000002947 alkylene group Chemical group 0.000 claims 5
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 5
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 5
- CHMBIJAOCISYEW-UHFFFAOYSA-N n-(4-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C=C1 CHMBIJAOCISYEW-UHFFFAOYSA-N 0.000 claims 5
- 229920002367 Polyisobutene Polymers 0.000 claims 4
- 125000004103 aminoalkyl group Chemical group 0.000 claims 4
- 150000004982 aromatic amines Chemical class 0.000 claims 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 4
- LHOVOJWYFIZPCY-UHFFFAOYSA-N 1,2,3-benzothiadiazol-4-amine Chemical compound NC1=CC=CC2=C1N=NS2 LHOVOJWYFIZPCY-UHFFFAOYSA-N 0.000 claims 3
- IHWDSEPNZDYMNF-UHFFFAOYSA-N 1H-indol-2-amine Chemical compound C1=CC=C2NC(N)=CC2=C1 IHWDSEPNZDYMNF-UHFFFAOYSA-N 0.000 claims 3
- QLSWIGRIBOSFMV-UHFFFAOYSA-N 1h-pyrrol-2-amine Chemical compound NC1=CC=CN1 QLSWIGRIBOSFMV-UHFFFAOYSA-N 0.000 claims 3
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims 3
- JWYUFVNJZUSCSM-UHFFFAOYSA-N 2-aminobenzimidazole Chemical compound C1=CC=C2NC(N)=NC2=C1 JWYUFVNJZUSCSM-UHFFFAOYSA-N 0.000 claims 3
- UHGULLIUJBCTEF-UHFFFAOYSA-N 2-aminobenzothiazole Chemical compound C1=CC=C2SC(N)=NC2=C1 UHGULLIUJBCTEF-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 3
- 150000003973 alkyl amines Chemical class 0.000 claims 3
- 150000001414 amino alcohols Chemical class 0.000 claims 3
- 150000005010 aminoquinolines Chemical class 0.000 claims 3
- 125000005365 aminothiol group Chemical class 0.000 claims 3
- 150000001448 anilines Chemical class 0.000 claims 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- 238000006243 chemical reaction Methods 0.000 claims 3
- 238000007334 copolymerization reaction Methods 0.000 claims 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 3
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 239000003999 initiator Substances 0.000 claims 3
- 239000000178 monomer Substances 0.000 claims 3
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims 3
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 229920005862 polyol Polymers 0.000 claims 3
- 229920000098 polyolefin Polymers 0.000 claims 3
- 150000003077 polyols Chemical class 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- XJCVRTZCHMZPBD-UHFFFAOYSA-N 3-nitroaniline Chemical compound NC1=CC=CC([N+]([O-])=O)=C1 XJCVRTZCHMZPBD-UHFFFAOYSA-N 0.000 claims 2
- UNBOSJFEZZJZLR-UHFFFAOYSA-N 4-(4-nitrophenylazo)aniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1 UNBOSJFEZZJZLR-UHFFFAOYSA-N 0.000 claims 2
- WOYZXEVUWXQVNV-UHFFFAOYSA-N 4-phenoxyaniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC=C1 WOYZXEVUWXQVNV-UHFFFAOYSA-N 0.000 claims 2
- QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 claims 2
- 150000004985 diamines Chemical class 0.000 claims 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 2
- 230000001050 lubricating effect Effects 0.000 claims 2
- 150000005673 monoalkenes Chemical class 0.000 claims 2
- 125000005702 oxyalkylene group Chemical group 0.000 claims 2
- UNDUSVBXIVZGOQ-UHFFFAOYSA-N 1h-perimidin-2-amine Chemical compound C1=CC(NC(N)=N2)=C3C2=CC=CC3=C1 UNDUSVBXIVZGOQ-UHFFFAOYSA-N 0.000 claims 1
- NAZDVUBIEPVUKE-UHFFFAOYSA-N 2,5-dimethoxyaniline Chemical compound COC1=CC=C(OC)C(N)=C1 NAZDVUBIEPVUKE-UHFFFAOYSA-N 0.000 claims 1
- YJKJAYFKPIUBAW-UHFFFAOYSA-N 9h-carbazol-1-amine Chemical compound N1C2=CC=CC=C2C2=C1C(N)=CC=C2 YJKJAYFKPIUBAW-UHFFFAOYSA-N 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 claims 1
- 125000006353 oxyethylene group Chemical group 0.000 claims 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 claims 1
- AYNUCZFIHUUAIZ-UHFFFAOYSA-N s-(2h-triazol-4-yl)thiohydroxylamine Chemical compound NSC1=CNN=N1 AYNUCZFIHUUAIZ-UHFFFAOYSA-N 0.000 claims 1
- 239000010802 sludge Substances 0.000 claims 1
- 239000004071 soot Substances 0.000 claims 1
- 0 CC=C(C=CC(*)=*=O)C([U]=CC)=N Chemical compound CC=C(C=CC(*)=*=O)C([U]=CC)=N 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/553941 | 2006-10-27 | ||
| US11/553,941 US7928044B2 (en) | 2006-10-27 | 2006-10-27 | Lubricating oil additive composition and method of making the same |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008111122A JP2008111122A (ja) | 2008-05-15 |
| JP2008111122A5 true JP2008111122A5 (enExample) | 2010-12-09 |
| JP5570692B2 JP5570692B2 (ja) | 2014-08-13 |
Family
ID=38920553
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007277358A Active JP5570692B2 (ja) | 2006-10-27 | 2007-10-25 | 潤滑油添加剤組成物およびその製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7928044B2 (enExample) |
| EP (1) | EP1916292B1 (enExample) |
| JP (1) | JP5570692B2 (enExample) |
| CN (1) | CN101168700B (enExample) |
| CA (1) | CA2606570C (enExample) |
| SG (1) | SG142283A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2869333A1 (en) | 2012-04-11 | 2013-10-17 | The Lubrizol Corporation | Dispersants derived from hydroxy fatty acid polyesters and polyalkylene glycol dispersants |
| US9145531B2 (en) | 2012-04-11 | 2015-09-29 | The Lubrizol Corporation | Amine terminated and hydroxyl terminated polyether dispersants |
| AU2016226303B2 (en) * | 2015-03-04 | 2020-11-26 | Huntsman Petrochemical Llc | Novel organic friction modifiers |
| US10344245B2 (en) | 2016-10-25 | 2019-07-09 | Chevron Oronite Technology B.V. | Lubricating oil compositions comprising a biodiesel fuel and a dispersant |
| US10781394B2 (en) | 2016-10-25 | 2020-09-22 | Chevron Oronite Technology B.V. | Lubricating oil compositions comprising a biodiesel fuel and a Mannich condensation product |
| CN108730770A (zh) | 2017-04-13 | 2018-11-02 | 通用电气公司 | 用于油的防蜡剂以及用防蜡剂来减少油产生蜡沉积的方法 |
| CN114031711B (zh) * | 2021-10-25 | 2023-04-28 | 上海应用技术大学 | 一种三元聚合物生物柴油降凝剂及制备方法 |
| US11820955B2 (en) | 2022-02-28 | 2023-11-21 | International Petroleum Products & Additives Company, Inc. | Dispersants derived from aromatic polyamines, lubricants, and methods |
| WO2024120884A1 (en) * | 2022-12-07 | 2024-06-13 | Basf Se | Aromatic amine modified acid-olefin copolymer for lubricants |
Family Cites Families (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3100673A (en) * | 1963-08-13 | Dyeings and prints possessing fastness | ||
| US2551813A (en) * | 1949-02-25 | 1951-05-08 | Du Pont | Free radical addition of h2s to olefins |
| US2992708A (en) * | 1954-01-14 | 1961-07-18 | Lyon George Albert | Air circulating wheel structure |
| DE1248643B (de) * | 1959-03-30 | 1967-08-31 | The Lubrizol Corporation, Cleveland, Ohio (V. St. A.) | Verfahren zur Herstellung von öllöslichen aeylierten Aminen |
| NL124842C (enExample) * | 1959-08-24 | |||
| NL255193A (enExample) * | 1959-08-24 | |||
| NL124306C (enExample) * | 1959-08-24 | |||
| US3381022A (en) * | 1963-04-23 | 1968-04-30 | Lubrizol Corp | Polymerized olefin substituted succinic acid esters |
| US3272746A (en) * | 1965-11-22 | 1966-09-13 | Lubrizol Corp | Lubricating composition containing an acylated nitrogen compound |
| US3560455A (en) * | 1969-05-26 | 1971-02-02 | Gulf Research Development Co | Process of forming copolymers of maleic anhydride and an aliphatic olefin having from 20 to 30 carbon atoms |
| US3912764A (en) * | 1972-09-29 | 1975-10-14 | Cooper Edwin Inc | Preparation of alkenyl succinic anhydrides |
| US3819660A (en) * | 1972-12-22 | 1974-06-25 | Standard Oil Co | Alkenylsuccinic anhydride preparation |
| US4240916A (en) * | 1976-07-09 | 1980-12-23 | Exxon Research & Engineering Co. | Pour point depressant additive for fuels and lubricants |
| DE2702604C2 (de) * | 1977-01-22 | 1984-08-30 | Basf Ag, 6700 Ludwigshafen | Polyisobutene |
| US4234435A (en) * | 1979-02-23 | 1980-11-18 | The Lubrizol Corporation | Novel carboxylic acid acylating agents, derivatives thereof, concentrate and lubricant compositions containing the same, and processes for their preparation |
| GB8329082D0 (en) * | 1983-11-01 | 1983-12-07 | Bp Chem Int Ltd | Low molecular weight polymers of 1-olefins |
| GB8818711D0 (en) | 1988-08-05 | 1988-09-07 | Shell Int Research | Lubricating oil dispersants |
| US5112507A (en) * | 1988-09-29 | 1992-05-12 | Chevron Research And Technology Company | Polymeric dispersants having alternating polyalkylene and succinic groups |
| IL91659A (en) * | 1989-09-15 | 1995-05-26 | Israel Min Of Energy & Inf | Geophysical survey system |
| GB9007267D0 (en) * | 1990-03-30 | 1990-05-30 | Shell Int Research | Process for preparing a dispersant/vi improver |
| US5241003A (en) * | 1990-05-17 | 1993-08-31 | Ethyl Petroleum Additives, Inc. | Ashless dispersants formed from substituted acylating agents and their production and use |
| US5139688A (en) * | 1990-08-06 | 1992-08-18 | Texaco, Inc. | Dispersant and antioxidant additive and lubricating oil composition containing same |
| US6117825A (en) * | 1992-05-07 | 2000-09-12 | Ethyl Corporation | Polyisobutylene succinimide and ethylene-propylene succinimide synergistic additives for lubricating oils compositions |
| US5286799A (en) | 1992-07-23 | 1994-02-15 | Chevron Research And Technology Company | Two-step free radical catalyzed process for the preparation of alkenyl succinic anhydride |
| US5319030A (en) * | 1992-07-23 | 1994-06-07 | Chevron Research And Technology Company | One-step process for the preparation of alkenyl succinic anhydride |
| EP0587381A1 (en) | 1992-09-09 | 1994-03-16 | BP Chemicals Limited | Novel derivatives of poly(iso)butene |
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| IL107927A0 (en) * | 1992-12-17 | 1994-04-12 | Exxon Chemical Patents Inc | Oil soluble ethylene/1-butene copolymers and lubricating oils containing the same |
| DE4330971A1 (de) | 1993-09-13 | 1995-03-16 | Basf Ag | Copolymerisate sowie deren Reaktionsprodukte mit Aminen als Kraftstoff- und Schmierstoffadditiv |
| GB9409346D0 (en) * | 1994-05-11 | 1994-06-29 | Bp Chemicals Additives | Lubricating oil additives |
| GB9523840D0 (en) | 1995-11-22 | 1996-01-24 | Bp Chemicals Additives | Lubricating oil additives |
| US5792729A (en) * | 1996-08-20 | 1998-08-11 | Chevron Chemical Corporation | Dispersant terpolymers |
| US6107258A (en) * | 1997-10-15 | 2000-08-22 | Ethyl Corporation | Functionalized olefin copolymer additives |
| CA2277412A1 (en) * | 1998-07-17 | 2000-01-17 | The Lubrizol Corporation | Engine oil having dispersant and aldehyde/epoxide for improved seal performance, sludge and deposit performance |
| US6015776A (en) * | 1998-09-08 | 2000-01-18 | Chevron Chemical Company | Polyalkylene polysuccinimides and post-treated derivatives thereof |
| US6156850A (en) * | 1998-09-16 | 2000-12-05 | Chevron Chemical Company Llc | Process for making polyalkenyl derivative of an unsaturated acidic reagent |
| EP0997517B1 (de) | 1998-10-27 | 2004-01-14 | Clariant GmbH | Polymermischungen zur Verbesserung der Schmierwirkung von Mitteldestillaten |
| US6451920B1 (en) | 1999-11-09 | 2002-09-17 | Chevron Chemical Company Llc | Process for making polyalkylene/maleic anhydride copolymer |
| DE60015606T2 (de) * | 1999-12-30 | 2005-10-20 | Uniroyal Chemical Co., Inc., Middlebury | Zusammensetzungen, enthaltend aminische antioxidantien auf basis von n-(4-anilinophenyl)amiden |
| US6770605B1 (en) | 2000-09-11 | 2004-08-03 | The Lubrizol Corporation | Modified polyisobutylene succinimide dispersants having improved seal, sludge, and deposit performance |
| US6906011B2 (en) | 2001-11-09 | 2005-06-14 | Chevron Oronite Company Llc | Polymeric dispersants prepared from copolymers of low molecular weight polyisobutene and unsaturated acidic reagent |
| US20040259742A1 (en) | 2003-06-18 | 2004-12-23 | Mishra Munmaya K. | Use of dispersant viscosity index improvers in exhaust gas recirculation engines |
| CN101031633B (zh) * | 2004-07-30 | 2010-11-10 | 卢布里佐尔公司 | 润滑配备有废气再循环的柴油机的方法 |
| 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 |
| US7618928B2 (en) | 2005-08-31 | 2009-11-17 | Chevron Oronite Company Llc | Lubricating oil additive composition and method of making the same |
-
2006
- 2006-10-27 US US11/553,941 patent/US7928044B2/en active Active
-
2007
- 2007-10-12 CA CA2606570A patent/CA2606570C/en active Active
- 2007-10-25 JP JP2007277358A patent/JP5570692B2/ja active Active
- 2007-10-26 SG SG200717234-9A patent/SG142283A1/en unknown
- 2007-10-26 EP EP07254241A patent/EP1916292B1/en active Active
- 2007-10-26 CN CN2007101678394A patent/CN101168700B/zh active Active
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