JP2008111127A5 - - Google Patents
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- Publication number
- JP2008111127A5 JP2008111127A5 JP2007279570A JP2007279570A JP2008111127A5 JP 2008111127 A5 JP2008111127 A5 JP 2008111127A5 JP 2007279570 A JP2007279570 A JP 2007279570A JP 2007279570 A JP2007279570 A JP 2007279570A JP 2008111127 A5 JP2008111127 A5 JP 2008111127A5
- Authority
- JP
- Japan
- Prior art keywords
- carbon atoms
- lubricating oil
- compound
- copolymer
- alkyl
- 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
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- 239000000203 mixture Substances 0.000 claims 63
- 125000004432 carbon atom Chemical group C* 0.000 claims 55
- 229920001577 copolymer Polymers 0.000 claims 53
- 239000010687 lubricating oil Substances 0.000 claims 53
- 125000000217 alkyl group Chemical group 0.000 claims 42
- 239000000654 additive Substances 0.000 claims 30
- 230000000996 additive effect Effects 0.000 claims 30
- 150000001875 compounds Chemical class 0.000 claims 29
- 150000002148 esters Chemical class 0.000 claims 28
- 229910052739 hydrogen Inorganic materials 0.000 claims 28
- 239000001257 hydrogen Substances 0.000 claims 28
- 125000003342 alkenyl group Chemical group 0.000 claims 26
- -1 monoolefin compound Chemical class 0.000 claims 23
- 125000003545 alkoxy group Chemical group 0.000 claims 22
- 125000003710 aryl alkyl group Chemical group 0.000 claims 22
- 125000002877 alkyl aryl group Chemical group 0.000 claims 21
- 150000002431 hydrogen Chemical class 0.000 claims 18
- 239000004721 Polyphenylene oxide Substances 0.000 claims 17
- 229920000570 polyether Polymers 0.000 claims 17
- 150000008064 anhydrides Chemical class 0.000 claims 14
- 150000001491 aromatic compounds Chemical class 0.000 claims 14
- 238000006555 catalytic reaction Methods 0.000 claims 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 10
- 150000001991 dicarboxylic acids Chemical class 0.000 claims 9
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 9
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 8
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 6
- 150000007824 aliphatic compounds Chemical class 0.000 claims 6
- 150000001336 alkenes Chemical class 0.000 claims 6
- 150000004982 aromatic amines Chemical class 0.000 claims 6
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 150000002763 monocarboxylic acids 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
- 229920002367 Polyisobutene Polymers 0.000 claims 5
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 claims 4
- MNLAVFKVRUQAKW-UHFFFAOYSA-N VR nerve agent Chemical compound CCN(CC)CCSP(C)(=O)OCC(C)C MNLAVFKVRUQAKW-UHFFFAOYSA-N 0.000 claims 4
- 229950003476 aminothiazole Drugs 0.000 claims 4
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 claims 4
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims 4
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 claims 4
- NFCPRRWCTNLGSN-UHFFFAOYSA-N 2-n-phenylbenzene-1,2-diamine Chemical group NC1=CC=CC=C1NC1=CC=CC=C1 NFCPRRWCTNLGSN-UHFFFAOYSA-N 0.000 claims 3
- 150000003973 alkyl amines Chemical class 0.000 claims 3
- 125000004103 aminoalkyl group Chemical group 0.000 claims 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 3
- 238000007334 copolymerization reaction Methods 0.000 claims 3
- 125000004663 dialkyl amino group Chemical group 0.000 claims 3
- 150000002391 heterocyclic compounds Chemical class 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 3
- 239000003999 initiator Substances 0.000 claims 3
- 239000000178 monomer Substances 0.000 claims 3
- CHMBIJAOCISYEW-UHFFFAOYSA-N n-(4-aminophenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C=C1 CHMBIJAOCISYEW-UHFFFAOYSA-N 0.000 claims 3
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims 3
- 239000003921 oil Substances 0.000 claims 3
- 229920000098 polyolefin Polymers 0.000 claims 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 3
- LHOVOJWYFIZPCY-UHFFFAOYSA-N 1,2,3-benzothiadiazol-4-amine Chemical compound NC1=CC=CC2=C1N=NS2 LHOVOJWYFIZPCY-UHFFFAOYSA-N 0.000 claims 2
- IHWDSEPNZDYMNF-UHFFFAOYSA-N 1H-indol-2-amine Chemical compound C1=CC=C2NC(N)=CC2=C1 IHWDSEPNZDYMNF-UHFFFAOYSA-N 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 2
- QLSWIGRIBOSFMV-UHFFFAOYSA-N 1h-pyrrol-2-amine Chemical compound NC1=CC=CN1 QLSWIGRIBOSFMV-UHFFFAOYSA-N 0.000 claims 2
- JWYUFVNJZUSCSM-UHFFFAOYSA-N 2-aminobenzimidazole Chemical compound C1=CC=C2NC(N)=NC2=C1 JWYUFVNJZUSCSM-UHFFFAOYSA-N 0.000 claims 2
- UHGULLIUJBCTEF-UHFFFAOYSA-N 2-aminobenzothiazole Chemical compound C1=CC=C2SC(N)=NC2=C1 UHGULLIUJBCTEF-UHFFFAOYSA-N 0.000 claims 2
- UIKUBYKUYUSRSM-UHFFFAOYSA-N 3-morpholinopropylamine Chemical compound NCCCN1CCOCC1 UIKUBYKUYUSRSM-UHFFFAOYSA-N 0.000 claims 2
- YJKJAYFKPIUBAW-UHFFFAOYSA-N 9h-carbazol-1-amine Chemical compound N1C2=CC=CC=C2C2=C1C(N)=CC=C2 YJKJAYFKPIUBAW-UHFFFAOYSA-N 0.000 claims 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 150000005010 aminoquinolines Chemical class 0.000 claims 2
- 150000001448 anilines Chemical class 0.000 claims 2
- 235000019445 benzyl alcohol Nutrition 0.000 claims 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 2
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 claims 2
- 230000001050 lubricating effect Effects 0.000 claims 2
- 150000005673 monoalkenes Chemical class 0.000 claims 2
- UDGSVBYJWHOHNN-UHFFFAOYSA-N n',n'-diethylethane-1,2-diamine Chemical compound CCN(CC)CCN UDGSVBYJWHOHNN-UHFFFAOYSA-N 0.000 claims 2
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 claims 2
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical group C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 claims 2
- AYNUCZFIHUUAIZ-UHFFFAOYSA-N s-(2h-triazol-4-yl)thiohydroxylamine Chemical compound NSC1=CNN=N1 AYNUCZFIHUUAIZ-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- XJCVRTZCHMZPBD-UHFFFAOYSA-N 3-nitroaniline Chemical compound NC1=CC=CC([N+]([O-])=O)=C1 XJCVRTZCHMZPBD-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- WOYZXEVUWXQVNV-UHFFFAOYSA-N 4-phenoxyaniline Chemical compound C1=CC(N)=CC=C1OC1=CC=CC=C1 WOYZXEVUWXQVNV-UHFFFAOYSA-N 0.000 claims 1
- QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical compound C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 238000002485 combustion reaction Methods 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 238000005461 lubrication Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000010802 sludge Substances 0.000 claims 1
- 239000004071 soot Substances 0.000 claims 1
- WZUUZPAYWFIBDF-UHFFFAOYSA-N Nc1n[nH]c(S)n1 Chemical compound Nc1n[nH]c(S)n1 WZUUZPAYWFIBDF-UHFFFAOYSA-N 0.000 description 2
- SWEICGMKXPNXNU-UHFFFAOYSA-N O=C1NNc2c1cccc2 Chemical compound O=C1NNc2c1cccc2 SWEICGMKXPNXNU-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N c1ccc2[nH]c3ccccc3c2c1 Chemical compound c1ccc2[nH]c3ccccc3c2c1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/553974 | 2006-10-27 | ||
| US11/553,974 US7820604B2 (en) | 2006-10-27 | 2006-10-27 | Lubricating oil additive composition and method of making the same |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008111127A JP2008111127A (ja) | 2008-05-15 |
| JP2008111127A5 true JP2008111127A5 (cg-RX-API-DMAC7.html) | 2010-12-09 |
| JP5383998B2 JP5383998B2 (ja) | 2014-01-08 |
Family
ID=38826452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007279570A Active JP5383998B2 (ja) | 2006-10-27 | 2007-10-26 | 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) | US7820604B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP1927650B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5383998B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN101168699B (cg-RX-API-DMAC7.html) |
| CA (1) | CA2605904C (cg-RX-API-DMAC7.html) |
| SG (1) | SG142280A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013154958A1 (en) | 2012-04-11 | 2013-10-17 | The Lubrizol Corporation | Amine terminated and hydroxyl terminated polyether dispersants |
| CA2869333A1 (en) | 2012-04-11 | 2013-10-17 | The Lubrizol Corporation | Dispersants derived from hydroxy fatty acid polyesters and polyalkylene glycol dispersants |
| JP6669760B2 (ja) * | 2015-03-04 | 2020-03-18 | ハンツマン ペトロケミカル エルエルシーＨｕｎｔｓｍａｎ Ｐｅｔｒｏｃｈｅｍｉｃａｌ ＬＬＣ | 新有機摩擦調整剤 |
| US9994786B2 (en) * | 2016-07-14 | 2018-06-12 | Chevron Oronite Company Llc | Polyester dispersants, synthesis and use thereof |
| 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 |
| US10344245B2 (en) | 2016-10-25 | 2019-07-09 | Chevron Oronite Technology B.V. | Lubricating oil compositions comprising a biodiesel fuel and a dispersant |
| 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 |
| US11999920B2 (en) | 2020-09-14 | 2024-06-04 | Ecolab Usa Inc. | Cold flow additives for plastic-derived synthetic feedstock |
| WO2022192577A1 (en) | 2021-03-10 | 2022-09-15 | Ecolab Usa Inc. | Stabilizer additives for plastic-derived synthetic feedstock |
| WO2023064375A1 (en) | 2021-10-14 | 2023-04-20 | Ecolab Usa Inc. | Antifouling agents for plastic-derived synthetic feedstocks |
| US11820955B2 (en) | 2022-02-28 | 2023-11-21 | International Petroleum Products & Additives Company, Inc. | Dispersants derived from aromatic polyamines, lubricants, and methods |
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| US3100673A (en) | 1963-08-13 | Dyeings and prints possessing fastness | ||
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| 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 (cg-RX-API-DMAC7.html) | 1959-08-24 | |||
| NL255194A (cg-RX-API-DMAC7.html) | 1959-08-24 | |||
| NL255193A (cg-RX-API-DMAC7.html) | 1959-08-24 | |||
| US3381022A (en) | 1963-04-23 | 1968-04-30 | Lubrizol Corp | Polymerized olefin substituted succinic acid esters |
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| CA2574969C (en) | 2004-07-30 | 2013-05-07 | The Lubrizol Corporation | Dispersant viscosity modifiers containing aromatic amines |
| US7700684B2 (en) * | 2004-12-09 | 2010-04-20 | Afton Chemical Corporation | Graft functionalized olefin polymer dispersant and uses thereof |
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-
2006
- 2006-10-27 US US11/553,974 patent/US7820604B2/en active Active
-
2007
- 2007-10-04 CA CA2605904A patent/CA2605904C/en active Active
- 2007-10-26 JP JP2007279570A patent/JP5383998B2/ja active Active
- 2007-10-26 SG SG200717230-7A patent/SG142280A1/en unknown
- 2007-10-26 CN CN200710167838.XA patent/CN101168699B/zh active Active
- 2007-10-26 EP EP07254253A patent/EP1927650B1/en active Active
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