CN101528895B - 曼尼希化合物的季铵盐 - Google Patents
曼尼希化合物的季铵盐 Download PDFInfo
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- CN101528895B CN101528895B CN2007800397917A CN200780039791A CN101528895B CN 101528895 B CN101528895 B CN 101528895B CN 2007800397917 A CN2007800397917 A CN 2007800397917A CN 200780039791 A CN200780039791 A CN 200780039791A CN 101528895 B CN101528895 B CN 101528895B
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- composition
- alkyl
- ammonium salt
- amino
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- 150000003242 quaternary ammonium salts Chemical class 0.000 title claims abstract description 45
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- 238000006683 Mannich reaction Methods 0.000 claims abstract description 41
- 150000001412 amines Chemical class 0.000 claims abstract description 33
- 238000006243 chemical reaction Methods 0.000 claims abstract description 33
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- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 21
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims abstract description 19
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims abstract 8
- -1 Alkyl epoxide Chemical class 0.000 claims description 74
- 125000000217 alkyl group Chemical group 0.000 claims description 63
- 239000007788 liquid Substances 0.000 claims description 48
- 239000003921 oil Substances 0.000 claims description 39
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 37
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- 229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 1
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- 108090000623 proteins and genes Proteins 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
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- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
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- 239000008117 stearic acid Substances 0.000 description 1
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- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 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
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
- C10M159/16—Reaction products obtained by Mannich reactions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
- C09D11/32—Inkjet printing inks characterised by colouring agents
- C09D11/324—Inkjet printing inks characterised by colouring agents containing carbon black
- C09D11/326—Inkjet printing inks characterised by colouring agents containing carbon black characterised by the pigment dispersant
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/221—Organic compounds containing nitrogen compounds of uncertain formula; reaction products where mixtures of compounds are obtained
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/22—Organic compounds containing nitrogen
- C10L1/234—Macromolecular compounds
- C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/18—Use of additives to fuels or fires for particular purposes use of detergents or dispersants for purposes not provided for in groups C10L10/02 - C10L10/16
-
- 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
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
-
- 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
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/042—Epoxides
-
- 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
- C10M2207/32—Esters of carbonic acid
-
- 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/02—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
- C10M2211/022—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
-
- 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
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
-
- 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/042—Sulfate esters
-
- 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
- C10N2030/04—Detergent property or dispersant property
-
- 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
- C10N2040/255—Gasoline engines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Combustion & Propulsion (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Paints Or Removers (AREA)
- Detergent Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Abstract
Description
清净剂 | 剂量率活性物(PTB) | 毫克/阀 |
对比例1 | 12.5 | 55.0 |
对比例1 | 12.5 | 84.0 |
对比例1 | 25.0 | 18.7 |
实施例1 | 12.5 | 5.0 |
实施例1 | 12.5 | 48.0 |
实施例1 | 8.4 | 64.0 |
Claims (17)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/469,690 US7906470B2 (en) | 2006-09-01 | 2006-09-01 | Quaternary ammonium salt of a Mannich compound |
US11/469,690 | 2006-09-01 | ||
PCT/US2007/076978 WO2008027881A2 (en) | 2006-09-01 | 2007-08-28 | Quaternary ammonium salt of a mannich compound |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101528895A CN101528895A (zh) | 2009-09-09 |
CN101528895B true CN101528895B (zh) | 2013-07-31 |
Family
ID=38884685
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2007800397917A Expired - Fee Related CN101528895B (zh) | 2006-09-01 | 2007-08-28 | 曼尼希化合物的季铵盐 |
Country Status (6)
Country | Link |
---|---|
US (2) | US7906470B2 (zh) |
EP (2) | EP2076582A2 (zh) |
JP (3) | JP2010502787A (zh) |
CN (1) | CN101528895B (zh) |
CA (1) | CA2662310A1 (zh) |
WO (1) | WO2008027881A2 (zh) |
Families Citing this family (97)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080113890A1 (en) * | 2006-11-09 | 2008-05-15 | The Lubrizol Corporation | Quaternary Ammonium Salt of a Polyalkene-Substituted Amine Compound |
WO2009040582A1 (en) | 2007-09-27 | 2009-04-02 | Innospec Limited | Fuel compositions |
EP2205704B1 (en) * | 2007-09-27 | 2015-08-26 | Innospec Limited | Fuel compositions |
MX2010011341A (es) * | 2008-05-15 | 2010-11-30 | Lubrizol Corp | Sales cuaternarias para su uso como tensioactivos en dispersiones. |
JP2010053352A (ja) * | 2008-07-31 | 2010-03-11 | Sanyo Chem Ind Ltd | 潤滑油添加剤及び潤滑油組成物 |
GB0903165D0 (en) * | 2009-02-25 | 2009-04-08 | Innospec Ltd | Methods and uses relating to fuel compositions |
CA2754219A1 (en) | 2009-03-03 | 2010-09-10 | Ewan E. Delbridge | Ashless or reduced ash quaternary detergents |
CN102597186B (zh) * | 2009-06-23 | 2015-07-01 | 罗地亚管理公司 | 增效清净剂及活性金属化合物的组合物 |
JP5427557B2 (ja) * | 2009-11-02 | 2014-02-26 | パイロットインキ株式会社 | ボールペン用水性インキ組成物及びそれを内蔵したボールペン |
BR112012011087A2 (pt) * | 2009-11-10 | 2016-07-05 | Lubrizol Corp | composicoes para limpeza de sistema lubrificante e seus métodos |
GB201001920D0 (en) * | 2010-02-05 | 2010-03-24 | Innospec Ltd | Fuel compostions |
GB201003973D0 (en) | 2010-03-10 | 2010-04-21 | Innospec Ltd | Fuel compositions |
GB201007756D0 (en) | 2010-05-10 | 2010-06-23 | Innospec Ltd | Composition, method and use |
US9006158B2 (en) | 2010-12-09 | 2015-04-14 | Basf Se | Polytetrahydrobenzoxazines and bistetrahydrobenzoxazines and use thereof as a fuel additive or lubricant additive |
CN103261175B (zh) | 2010-12-09 | 2016-05-25 | 巴斯夫欧洲公司 | 聚四氢苯并噁嗪和双四氢苯并噁嗪及其作为燃料添加剂或润滑剂添加剂的用途 |
EP2554636A1 (en) * | 2011-08-03 | 2013-02-06 | Innospec Limited | Fuel compositions |
GB201113388D0 (en) * | 2011-08-03 | 2011-09-21 | Innospec Ltd | Fuel compositions |
CA2849633A1 (en) * | 2011-09-23 | 2013-03-28 | The Lubrizol Corporation | Quaternary ammonium salts in heating oils |
US9574149B2 (en) | 2011-11-11 | 2017-02-21 | Afton Chemical Corporation | Fuel additive for improved performance of direct fuel injected engines |
US8690970B2 (en) | 2012-02-24 | 2014-04-08 | Afton Chemical Corporation | Fuel additive for improved performance in fuel injected engines |
CA2869329A1 (en) | 2012-04-04 | 2013-10-10 | The Lubrizol Corporation | Bearing lubricants for pulverizing equipment |
US8894726B2 (en) | 2012-06-13 | 2014-11-25 | Afton Chemical Corporation | Fuel additive for improved performance in fuel injected engines |
CN103589413B (zh) * | 2012-08-13 | 2016-11-02 | 中国石油天然气股份有限公司 | 一种油井酸化缓蚀剂及其制备和应用 |
US9206373B2 (en) * | 2012-08-17 | 2015-12-08 | Afton Chemical Corporation | Calcium neutral and overbased mannich and anhydride adducts as detergents for engine oil lubricants |
CA2887256A1 (en) | 2012-10-23 | 2014-05-01 | The Lubrizol Corporation | Diesel detergent without a low molecular weight penalty |
BR112015008939A2 (pt) | 2012-10-23 | 2017-07-04 | Basf Se | uso de um produto de reação |
US9458400B2 (en) | 2012-11-02 | 2016-10-04 | Afton Chemical Corporation | Fuel additive for improved performance in direct fuel injected engines |
US9017431B2 (en) | 2013-01-16 | 2015-04-28 | Afton Chemical Corporation | Gasoline fuel composition for improved performance in fuel injected engines |
GB201313423D0 (en) * | 2013-07-26 | 2013-09-11 | Innospec Ltd | Compositions and methods |
KR102453736B1 (ko) | 2013-07-26 | 2022-10-11 | 이노스펙 리미티드 | 연료 조성물 |
US9464252B2 (en) | 2013-10-08 | 2016-10-11 | Afton Chemical Corporation | Quaternary ammonium detergent fuel additives |
US8974551B1 (en) | 2014-02-19 | 2015-03-10 | Afton Chemical Corporation | Fuel additive for improved performance in fuel injected engines |
FR3017876B1 (fr) | 2014-02-24 | 2016-03-11 | Total Marketing Services | Composition d'additifs et carburant de performance comprenant une telle composition |
FR3017875B1 (fr) * | 2014-02-24 | 2016-03-11 | Total Marketing Services | Composition d'additifs et carburant de performance comprenant une telle composition |
CA2946865C (en) | 2014-04-25 | 2023-03-28 | The Lubrizol Corporation | Multigrade lubricating compositions |
EP3517593A1 (en) | 2014-05-30 | 2019-07-31 | The Lubrizol Corporation | Low molecular weight amide/ester containing quaternary ammonium salts |
US20170107441A1 (en) | 2014-05-30 | 2017-04-20 | The Lubrizol Corporation | Epoxide quaternized quaternary ammonium salts |
US20170101594A1 (en) | 2014-05-30 | 2017-04-13 | The Lubrizol Corporation | Coupled quaternary ammonium salts |
CN106661472A (zh) | 2014-05-30 | 2017-05-10 | 路博润公司 | 高分子量的含酰胺/酯的季铵盐 |
US20170114297A1 (en) | 2014-05-30 | 2017-04-27 | The Lubrizol Corporation | Imidazole containing quaternary ammonium salts |
US20170107438A1 (en) | 2014-05-30 | 2017-04-20 | The Lubrizol Corporation | High molecular weight imide containing quaternary ammonium salts |
CN106574197A (zh) | 2014-05-30 | 2017-04-19 | 路博润公司 | 含支链胺的季铵盐 |
CN113684073A (zh) | 2014-05-30 | 2021-11-23 | 路博润公司 | 低分子量含酰亚胺季铵盐 |
EP2987845B1 (en) * | 2014-08-19 | 2018-05-09 | Afton Chemical Corporation | Use of quaternary ammonium salts in gasoline fuel to improve performance |
CN107735485A (zh) | 2015-03-25 | 2018-02-23 | 路博润公司 | 用于直喷式发动机的润滑剂组合物 |
US9340742B1 (en) | 2015-05-05 | 2016-05-17 | Afton Chemical Corporation | Fuel additive for improved injector performance |
GB201513304D0 (en) | 2015-07-28 | 2015-09-09 | Innospec Ltd | Compositions and Methods |
SG10202005167TA (en) | 2015-12-02 | 2020-07-29 | Lubrizol Corp | Ultra-low molecular weight amide/ester containing quaternary ammonium salts having short hydrocarbon tails |
SG11201804227UA (en) | 2015-12-02 | 2018-06-28 | Lubrizol Corp | Ultra-low molecular weight imide containing quaternary ammonium salts having short hydrocarbon tails |
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GB201705091D0 (en) | 2017-03-30 | 2017-05-17 | Innospec Ltd | Compositions and methods and uses relating thereto |
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EP3684890A2 (en) | 2017-09-21 | 2020-07-29 | The Lubrizol Corporation | Polyacrylate antifoam components for use in fuels |
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Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4071327A (en) * | 1973-11-07 | 1978-01-31 | The Lubrizol Corporation | Salts of Mannich bases and derivatives thereof |
Family Cites Families (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DD39618A (zh) * | ||||
US2635100A (en) * | 1949-11-15 | 1953-04-14 | Du Pont | Monoquaternary ammonium carbonates and their preparation |
US3468816A (en) * | 1964-07-24 | 1969-09-23 | Nalco Chemical Co | Method of purifying an impure quaternary ammonium salt by addition of an epoxide |
US3401119A (en) * | 1965-02-16 | 1968-09-10 | Emery Industries Inc | Quaternary ammonium compounds and process of making |
US3790606A (en) * | 1970-09-30 | 1974-02-05 | Diamond Shamrock Corp | Alkoxylated mannich compositions and derivatives thereof |
US3749695A (en) * | 1971-08-30 | 1973-07-31 | Chevron Res | Lubricating oil additives |
BE793279A (fr) | 1971-12-30 | 1973-06-22 | Ici Ltd | Agents dispersants |
US3778371A (en) * | 1972-05-19 | 1973-12-11 | Ethyl Corp | Lubricant and fuel compositions |
US4056531A (en) * | 1973-09-07 | 1977-11-01 | Ethyl Corporation | Polymonoolefin quaternary ammonium salts of triethylenediamine |
US4108858A (en) * | 1975-09-15 | 1978-08-22 | Ethyl Corporation | Polyolefin quaternary pyridinium salts |
US4179424A (en) * | 1977-11-21 | 1979-12-18 | Nalco Chemical Company | Method for rapidly producing amino methylated polymers and quaternary ammonium salts thereof |
US4171959A (en) * | 1977-12-14 | 1979-10-23 | Texaco Inc. | Fuel composition containing quaternary ammonium salts of succinimides |
US4253980A (en) * | 1979-06-28 | 1981-03-03 | Texaco Inc. | Quaternary ammonium salt of ester-lactone and hydrocarbon oil containing same |
US4306070A (en) * | 1979-06-28 | 1981-12-15 | Texaco Inc. | Method for preparing quaternary ammonium salt of ester-lactone |
US4326973A (en) * | 1981-01-13 | 1982-04-27 | Texaco Inc. | Quaternary ammonium succinimide salt composition and lubricating oil containing same |
US4338206A (en) * | 1981-03-23 | 1982-07-06 | Texaco Inc. | Quaternary ammonium succinimide salt composition and lubricating oil containing same |
JPS61106544A (ja) * | 1984-10-30 | 1986-05-24 | Kao Corp | 第四級アンモニウム塩の製造法 |
DE3732908A1 (de) | 1987-09-30 | 1989-04-13 | Basf Ag | Polyetheramine enthaltende kraftstoffe fuer ottomotoren |
JPH0819351B2 (ja) * | 1988-06-09 | 1996-02-28 | サカタインクス株式会社 | 顔料分散剤及びそれを用いたオフセット印刷インキ組成物 |
US5039310A (en) * | 1988-12-06 | 1991-08-13 | Mobil Oil Corporation | Polyether substituted mannich bases as fuel and lubricant ashless dispersants |
US5094667A (en) | 1990-03-20 | 1992-03-10 | Exxon Research And Engineering Company | Guerbet alkyl ether mono amines |
DE4128637A1 (de) * | 1990-09-05 | 1992-03-12 | Sandoz Ag | Derivate von mannichkondensationsprodukten, deren herstellung und verwendung |
US5944858A (en) * | 1990-09-20 | 1999-08-31 | Ethyl Petroleum Additives, Ltd. | Hydrocarbonaceous fuel compositions and additives therefor |
US5254138A (en) * | 1991-05-03 | 1993-10-19 | Uop | Fuel composition containing a quaternary ammonium salt |
US5503644A (en) | 1991-09-23 | 1996-04-02 | Shell Oil Company | Gasoline composition for reducing intake valve deposits in port fuel injected engines |
US5697988A (en) * | 1991-11-18 | 1997-12-16 | Ethyl Corporation | Fuel compositions |
US5279626A (en) * | 1992-06-02 | 1994-01-18 | Ethyl Petroleum Additives Inc. | Enhanced fuel additive concentrate |
US5399178A (en) * | 1993-12-17 | 1995-03-21 | Chevron Chemical Company | Mannich condensation products of polyalkylene hydroxyaromatic esters and fuel compositions containing the same |
US5721358A (en) * | 1994-04-28 | 1998-02-24 | Toyo Ink Manufacturing Co., Ltd. | Process for the production of copper phthalocyanine |
US5482523A (en) * | 1994-11-02 | 1996-01-09 | Chevron Chemical Company | Mannich condensation products of poly(oxyalkylene) hydroxyaromatic ethers and fuel compositions containing the same |
JP3662931B2 (ja) * | 1994-12-13 | 2005-06-22 | エクソン ケミカル パテンツ インコーポレイテッド | 燃料油組成物 |
US5634951A (en) * | 1996-06-07 | 1997-06-03 | Ethyl Corporation | Additives for minimizing intake valve deposits, and their use |
US5725612A (en) * | 1996-06-07 | 1998-03-10 | Ethyl Corporation | Additives for minimizing intake valve deposits, and their use |
GB9618546D0 (en) * | 1996-09-05 | 1996-10-16 | Bp Chemicals Additives | Dispersants/detergents for hydrocarbons fuels |
US6048373A (en) * | 1998-11-30 | 2000-04-11 | Ethyl Corporation | Fuels compositions containing polybutenes of narrow molecular weight distribution |
US6403725B1 (en) * | 1999-08-20 | 2002-06-11 | The Lubrizol Corporation | Metal containing dispersant polymers from condensation of polymers containing acidic group with overbased compositions containing reactive nucleophilic group |
US6800103B2 (en) * | 2001-02-02 | 2004-10-05 | Ethyl Corporation | Secondary amine mannich detergents |
US7795192B2 (en) * | 2002-04-19 | 2010-09-14 | The Lubrizol Corporation | Lubricant composition suitable for direct fuel injected, crankcase-scavenged two-stroke engines |
US6699319B2 (en) * | 2002-05-06 | 2004-03-02 | Cabot Corporation | Process for preparing modified pigments |
EP1585773A1 (en) | 2003-01-21 | 2005-10-19 | The Lubrizol Corporation | Low color polyisobutylene succinic anhydride-derived emulsifiers |
DE10307728B4 (de) * | 2003-02-24 | 2005-09-22 | Clariant Gmbh | Korrosions-und Gashydratinhibitoren mit verbesserter Wasserlöslichkeit und erhöhter biologischer Abbaubarkeit und derartige Verbindungen |
EP1475411A1 (de) * | 2003-05-05 | 2004-11-10 | Sika Technology AG | Mannichbasen und Herstellungsverfahren von Mannichbasen |
JP4790208B2 (ja) * | 2003-06-24 | 2011-10-12 | 中国塗料株式会社 | エポキシ樹脂組成物、該組成物から形成された防食皮膜、および該防食皮膜で被覆された防食皮膜付き基材、並びに基材の防食方法 |
US7256161B2 (en) * | 2003-11-13 | 2007-08-14 | Chevron Oronite Company Llc | Process for making group II metal carbonated, overbased Mannich condensation products of alkylphenols |
US7618467B2 (en) * | 2004-01-29 | 2009-11-17 | Chemtura Corporation | Detergent / anti-oxidant additives for fuels and lubricants |
MX2010011341A (es) * | 2008-05-15 | 2010-11-30 | Lubrizol Corp | Sales cuaternarias para su uso como tensioactivos en dispersiones. |
-
2006
- 2006-09-01 US US11/469,690 patent/US7906470B2/en active Active
-
2007
- 2007-08-28 CA CA002662310A patent/CA2662310A1/en not_active Abandoned
- 2007-08-28 CN CN2007800397917A patent/CN101528895B/zh not_active Expired - Fee Related
- 2007-08-28 EP EP07841457A patent/EP2076582A2/en not_active Ceased
- 2007-08-28 WO PCT/US2007/076978 patent/WO2008027881A2/en active Application Filing
- 2007-08-28 JP JP2009526864A patent/JP2010502787A/ja active Pending
- 2007-08-28 EP EP12154759A patent/EP2457981A1/en not_active Withdrawn
-
2011
- 2011-01-31 US US13/017,066 patent/US8083814B2/en active Active
-
2013
- 2013-01-24 JP JP2013010901A patent/JP5793517B2/ja not_active Expired - Fee Related
-
2015
- 2015-08-10 JP JP2015158122A patent/JP2015214712A/ja active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4071327A (en) * | 1973-11-07 | 1978-01-31 | The Lubrizol Corporation | Salts of Mannich bases and derivatives thereof |
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WO2008027881A3 (en) | 2008-05-29 |
WO2008027881A2 (en) | 2008-03-06 |
JP2013079284A (ja) | 2013-05-02 |
US8083814B2 (en) | 2011-12-27 |
JP2015214712A (ja) | 2015-12-03 |
CA2662310A1 (en) | 2008-03-06 |
CN101528895A (zh) | 2009-09-09 |
EP2457981A1 (en) | 2012-05-30 |
JP5793517B2 (ja) | 2015-10-14 |
EP2076582A2 (en) | 2009-07-08 |
US7906470B2 (en) | 2011-03-15 |
US20110130317A1 (en) | 2011-06-02 |
JP2010502787A (ja) | 2010-01-28 |
US20080052985A1 (en) | 2008-03-06 |
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