EP0072645A2 - Succinimide dispersant amélioré pour huile lubrifiante - Google Patents

Succinimide dispersant amélioré pour huile lubrifiante Download PDF

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Publication number
EP0072645A2
EP0072645A2 EP82304066A EP82304066A EP0072645A2 EP 0072645 A2 EP0072645 A2 EP 0072645A2 EP 82304066 A EP82304066 A EP 82304066A EP 82304066 A EP82304066 A EP 82304066A EP 0072645 A2 EP0072645 A2 EP 0072645A2
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EP
European Patent Office
Prior art keywords
anhydride
polyamine
composition
dispersant
lubricating oil
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.)
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EP82304066A
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German (de)
English (en)
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EP0072645A3 (en
EP0072645B1 (fr
Inventor
Max Jay Wisotsky
Ricardo Alfredo Bloch
Darrell William Brownawell
Frank Joung-Yei Chen
Antonio Gutierrez
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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Publication of EP0072645A3 publication Critical patent/EP0072645A3/en
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    • C10M133/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
    • C10M133/52Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
    • C10M133/56Amides; Imides
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    • C10M2203/06Well-defined aromatic compounds
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    • C10M2205/06Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
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    • C10M2217/04Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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    • C10M2219/108Phenothiazine
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    • C10N2070/02Concentrating of additives
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02BINTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
    • F02B1/00Engines characterised by fuel-air mixture compression
    • F02B1/02Engines characterised by fuel-air mixture compression with positive ignition
    • F02B1/04Engines characterised by fuel-air mixture compression with positive ignition with fuel-air mixture admission into cylinder
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
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    • F02B3/00Engines characterised by air compression and subsequent fuel addition
    • F02B3/06Engines characterised by air compression and subsequent fuel addition with compression ignition

Definitions

  • This invention relates to lubricating oil dispersants which exhibit highly effective dispersant potency in both gasoline and diesel engines. More particularly, the invention relates to lubricating oil compositions for use both in gasoline and diesel engine formulations which meet current performance requirements for both types of engines, the formulations being characterized as containing novel dispersants prepared in a particular reaction sequence.
  • a current objective in the industry is to provide lubricating oil compositions which meet or exceed engine qualification standards of dispersancy for both gasoline and diesel or compression ignition engines.
  • dispersants have been developed which meet one or the other of these requirements, but development of a dispersant which satisfies the highest service classification requirements of the relevant engine qualification tests for both types of oils has not been entirely successful. It is an object of the present invention to provide lubricating oil compositions containing novel dispersants which meet these goals.
  • the present invention is within the broad field of improved polyolefin, particularly polyisobutenyl, succinic acid or anhydride-polyamine reaction product dispersants, and such dispersants are disclosed generally, for example, in U.S. Patent 3,172,892 issued March 9, 1965 to LeSuer et al.
  • U.S. Patent 3,216,936 issued November 9, 1965 to LeSuer shows lubricating oil additives prepared by acylation of an alkylene amine with both a polyolefin succinic anhydride and an aliphatic monocarboxylic acid, preferably a mono acid having more than 12 carbon atoms such as stearic or oleic acid.
  • the products can be prepared by reacting both acidic compounds simultaneously with a polyamine or by first reacting the polyolefin succinic acid with polyamine and subsequently with monocarboxylic acid.
  • the products so formed are said to be particularly useful in improving the thermal stability of lubricating compositions which contain metal phosphorodithioates.
  • British Patent 1,018,982 (1966) discloses lubricating oil additives which are the reaction products of three components: alkenyl succinic anhydrides, polyamines and carboxylic acids and the products are said to have improved sludge dispersant properties.
  • alkenyl succinic anhydrides are those similar to the materials of the present invention, i.e., preferably polyisobutenyl succinic anhydrides and the polyamines are also similar, i.e., the alkylene polyamines.
  • the carboxylic acids of this reference are disclosed as being mono- or di- carboxylic acids having 1 to 30, preferably 1 to 18 carbon atoms, with acetic acid being preferred since it forms an imidazoline or pyrimidine with a minimum of carbon atoms.
  • This reference also states that lower molecular weight carboxylic acids are more effective in promoting the sludge dispersing activity of the final product.
  • the preparative method disclosed in British Patent 1,018,982 comprises either first reacting the carboxylic acid and the polyamine in what is described as an imidazoline or pyrimidine forming reaction with subsequent reaction with alkenyl succinic anhydride or by reacting the three materials simultaneously.
  • U.S. Patent 3,415,750 issued December 10, 1968 to Anzenberger discloses lubricant additives categorized as imidazolines which are prepared by reacting a polyethylene polyamine with a mono-carboxylic acid or a di- carboxylic acid to form a heterocyclic imidazoline intermediate which is subsequently reacted with a polyalkenyl succinic anhydride to provide a bis-imidazoline which is said to have improved detergency and dispersancy in lubricating oil formulations.
  • U.S. Patent 3,374,174 issued March 19, 1968 to LeSuer discloses lubricant additives prepared by reacting amines, including alkylene polyamines, with both a high molecular weight saturated monocarboxylic acid and a dicarboxylic acid or anhydride, preferably those having up to 12 carbons.
  • the patent discloses the simultaneous reaction of all three materials or a sequential process whereby there is first formed an acylated amine intermediate with the amine and high molecular weight carboxylic acid which is subsequently reacted with the dicarboxylic acid reactant.
  • U.S. 4,173,540 discloses the reaction of polyisobutenyl succinic anhydride with polyamines in a molar ratio of 2.0 to 2.5 moles of anhydride per mole of polyamine to provide a diimide dispersant, however, such products will not meet the requirements for both gasoline and diesel engine formulations.
  • U.S. 3,401,118 discloses reacting tetraethylene pentamine first with polyisobutenyl succinic anhydride (PIBSA) derived from 850-1200 M n polyisobutylene and then reacting this intermediate with PIBSA derived from polyisobutylene of 400-750 M n ; the 400 M n corresponding to 29 carbon atoms.
  • PIBSA polyisobutenyl succinic anhydride
  • the present invention distinguishes from these references in requiring a particular reaction sequence characterized by the use of a dicarboxylic acid anhydride in the final step and an overall mole ratio of anhydride to polyamine within a relatively narrow and critically defined range. These parameters have been found essential to provide lubricating oil compositions which give demonstrated performance values in engine tests required to qualify for the highest grade service classifications for both gasoline and diesel engine lubricating oils.
  • the reaction sequence is particularly critical; thus products prepared in a simultaneous reaction technique will not meet the objectives of this invention.
  • lubricating oil compositions exhibiting improved dispersancy in both gasoline and diesel engines comprising a major amount of lubricating oil and an effective amount of a polyalkenyl succinimide dispersant, said dispersant being prepared in a two-step sequential process comprising (a) first reacting a polyalkenyl succinic anhydride, the polyalkenyl being a polymer of a C 3 or C 4 olefin,and an alkylene polyamine of the formula H 2 N(CH 2 ) n (NH(CH 2 ) n ) m NH 2 , wherein n is 2 or 3 and m is 0 to 10 in a molar ratio of about 1.0 to 2.2 moles of succinic anhydride per mole of polyamine, and (b) reacting the product of step (a) with a di-carboxylic acid anhydride selected from the group consisting of maleic anhydride, succinic anhydride and C 1
  • the polyalkenyl succinic anhydrides useful in the present invention generally comprise those wherein the polyalkenyl group has a Bn (number average molecular weight) of about 700 to 5,000, preferably 900 to 2,000.
  • Bn number average molecular weight
  • the methods of preparation are well known in the art, i.e., reaction of maleic anhydride with either the polyolefin itself or with a chlorinated polyolefin which in either case provides the desired polyalkenyl succinic anhydride.
  • Polyisobutylene is preferred but other polymers of C 3 or C 4 olefins such as polybutene-1 and polypropylene are suitable including mixtures of such polyolefins.
  • Suitable alkylene polyamines are also well known represented by the formula NH 2 (CH 2 ) n (NH(CH 2 ) n ) m NH 2 , wherein n is 2 to 3 and m is 0 to 10.
  • Illustrative are ethylene diamine, diethylene triamine, triethylene tetramine, tetraethylene pentamine, pentaethylene hexamine, and the like.
  • -Preferred for use is tetraethylene p entamine or a mixture of ethylene polyamines which approximates tetraethylene pentamine such as "DOW E-100" (a commercial mixture available from Dow Chemical Company, Midland, Michigan).
  • polyalkenyl succinimide dispersant or diimide dispersant as used herein is meant to encompass the completed reaction product of the sequential process and is intended to encompass compounds wherein the product may have amide, amidine or salt linkages in addition to the imide linkage which results from the reaction of the primary amino group and the anhydride moiety.
  • the third reactant used to prepare the dispersants of the present invention encompasses maleic anhydride, succinic anhydride or an alkenyl or alkyl succinic anhydride having up to about 18 carbon atoms and preferably at least 8 carbon atoms.
  • Particularly advantageous results in terms of engine performance data have been obtained with dodecenyl succinic anhydride and maleic anhydride and the use of these materials, and the dispersants produced thereby, represent particularly preferred embodiments.
  • both the reaction sequence and the overall final mole ratio of total succinic anhydride groups to polyamine in the finished product have been found to be essential to meet the objective of passing both engine qualification tests for gasoline and diesel lubricating oil formulations.
  • the reaction sequence requires a first step in the preparation of a polyisobutenyl succinic anhydride-polyamine reaction product. These are reacted in a mole ratio of about 1.0 to 2.2 moles of polyisobutenyl succinic anhydride per mole of polyamine.
  • Suitable solvent oils are the same as the oils used as a lubricating oil base stock and these generally include lubricating oils having a viscosity (ASTM D-445) of about 2 to 40, preferably 5 to 20,centistokes at 99 0 C, with the primarily paraffinic mineral oils being particularly preferred, such as Solvent 150 Neutral.
  • Lubricating oil compositions are prepared containing the dispersant of the present invention together with conventional amounts of other additives to provide their normal attendant functions such as viscosity index improvers, rust inhibitors, metal detergent additives, antioxidants, and zinc dialkyldithiophosphates anti-wear additives and these compositions meet the objective of passing engine qualification tests for both gasoline and diesel engine usage.
  • lubricating oil formulations must equal or exceed certain values in the MS Sequence VD Engine Test (ASTM Special Publication 315).
  • MS Sequence VD Engine Test ASTM Special Publication 315).
  • the significant values in this test are a minimum of 9.4 sludge, 6.7 piston skirt varnish and 6.6 average varnish.
  • the Sequence VD uses a 1980 Ford 2.3 liter 4-cylinder engine and is a 192-hour test comprising the cyclic operation at varying engine speeds and temperatures to simulate "stop and go" city driving and moderate turn p ike operation.
  • the test is an established industry standard.
  • the Caterpillar 1-H/2 test is the current standard to evaluate the effects of a crankcase oil on ring sticking and piston deposits. The test simulates high speed, moderately supercharged engine operation. This test is also Federal Test Method 791-346 and is used to meet military specifications such as MIL-L-21260B and industry specifications such as SAE 183 and General Motors GM6146M.
  • WTD Weighted Total Demerits
  • WTD is a cumulative rating based on observation of deposits in the groove and land areas of the piston and lacquer on piston skirts with all the specific evaluation being rated according to their relative importance and the final WTD being calculated in accordance with the test procedure.
  • the dispersants prepared according to the invention can be incorporated in a wide variety of lubricants. They can be used in lubricating oil compositions, such as automotive crankcase lubricating oils, automatic transmission fluids, etc. in effective amounts to provide active ingredient concentrations in finished formulations generally within the range of about 0.5 to 10 weight percent, for example, 1 to 5 weight percent, preferably 1.5 to 3 weight percent, of the total composition. Conventionally, the dispersants are admixed with the lubricating oils as dispersant solution concentrates which usually contain up to about 50 percent weight of the active ingredient additive compound dissolved in mineral oil, preferably a mineral oil having an ASTM D-445 viscosity of about 2 to 40, preferably 5 to 20 centistokes at 99°C.
  • mineral oil preferably a mineral oil having an ASTM D-445 viscosity of about 2 to 40, preferably 5 to 20 centistokes at 99°C.
  • the lubricating oil includes not only hydrocarbon oils of lubricating viscosity derived from petroleum but also includes synthetic lubricating oils such as polyethylene oils; alkyl esters of dicarboxylic acids, complex esters of dicarboxylic acid, polyglycol and alcohol; alkyl esters of carbonic or phosphoric acids; polysilicones; fluorohydrocarbon oils; and mixture's or lubricating oils and synthetic oils in any proportion, etc.
  • the term "lubricating oil" for this disclosure includes all the foregoing.
  • the useful dispersant may be conveniently dispersed as a concentrate of 10 to 80 weight percent, preferably up to about 50 weight percent, of said dispersant in 20 to 90 weight percent of mineral oil, e.g., Solvent 150 Neutral oil with or without other additives being present and such concentrates are a further embodiment of this invention.
  • mineral oil e.g., Solvent 150 Neutral oil with or without other additives being present and such concentrates are a further embodiment of this invention.
  • Such lubricating oil compositions containing the dispersants of the present invention will also contain other well-known additives such as the zinc dialkyl (C 3 -Cg) dithiophosphate anti-wear inhibitors, generally present in amounts of about 1 to 5 weight percent.
  • Useful detergents include the oil-soluble normal basic or over-based metal, e.g., calcium, magnesium, barium, etc., salts of petroleum naphthenic acids, petroleum sulfonic acids, alkyl benzene sulfonic acids, oil-soluble fatty acids, alkyl salicylic acids, alkylene bis-phenols and hydrolyzed phosphosulfurized polyolefins.
  • Typical amounts are from 1 to 7 weight percent with the HD or diesel oils usually containing slightly more of this metal detergent additive.
  • Preferred detergents are the calcium and magnesium normal or overbased phenates, sulfurized phenates or sulfonates.
  • Diesel lubricating oils preferably contain 4-6 percent of this additive.
  • Oxidation inhibitors include hindered phenols, e.g., 2.6-ditertbutyl-para-cresol, amines, sulfurized phenols and alkyl phenothiazines usually present in amounts of from 0.001 to 1 weight percent.
  • Pour point depressants which may be present in amounts of from 0.01 to 1 weight percent include wax alkylated aromatic hydrocarbons, olefin polymers and copolymers, acrylate and methacrylate polymers and copolymers.
  • Viscosity index improvers which may vary from about 1 to 15 weight percent depending on the viscosity grade required include olefin polymers such as polybutene, ethylene-propylene copolymers, hydrogenated polymers and copolymers and terpolymers of styrene with isoprene and/or butadiene, polymers of alkyl acrylates or alkyl methacrylates, copolymers of alkyl methacrylates with N-vinyl pyrrolidone or dimethylaminoalkyl methacrylate, post-grafted polymers of ethylene-propylene with an active monomer such as maleic anhydride which may be further reacted with an alcohol or an alkylene polyamine, styrene/maleic anhydride polymers post-treated with alcohols and amines, etc.
  • olefin polymers such as polybutene, ethylene-propylene copolymers, hydrogenated polymers and copolymers and ter
  • Rust inhibition activity can be provided by about 0.01 to 1 weight percent of the afore-mentioned metal dihydrocarbyl dithiophosphates and the corresponding precursor esters,phosphosulfurized pinenes, sulfurized olefins and hydrocarbons, sulfurized fatty esters and sulfurized alkyl phenols.
  • Preferred are the zinc dihydrocarbyl dithiophosphates which are salts of dihydrocarbyl esters of dithiophosphoric acids.
  • additives include effective amounts of the fuel economy additives or friction reducing additives such as the dimer acid esters, as disclosed in U.S. 4,105,571 to Shaub et al, which are present in amounts of about 1 to 5 weight percent with esters of dimerized linoleic acid and diethylene glycol being a preferred material.
  • Glycerol oleates are another example of fuel economy additives and these are usually present in very small amounts, such as 0.05 to 0.2 weight percent based on the weight of the formulated oil.
  • Example 2 320 grams of the inital PIBSA/polyamine product of Example 1 being the same but having a mole ratio of 2.1 mole of succinic anhydride per mole of polyamine was reacted with 6.0 grams of dodecenyl succinic anhydride in Solvent 150 Neutral at 160 o C for 2 hours to provide a product having a final mole ratio of 2.4 moles of anhydride per mole of polyamine. The product analyzed for 1.50 percent N.
  • Example 2 was repeated except that 2.2 grams of maleic anhydride was used to provide a product having a final mole ratio of 2.4 moles of anhydride per mole of polyamine. The product analyzed for 1.53 percent N.
  • Example 3 The product of Example 3 was included as the dispersant at a concentration of 3.6 weight percent active ingredient in a formulated SAE 10W40 lubricating oil composition and subjected to the ASTM Sequence V-D engine test for gasoline engines.
  • the formulation also contained conventional amounts of overbased sulfonate, zinc dialkyl dithiophosphate, antioxidant, olefin copolymer viscosity index improver, rust inhibitor and anti-foam additive.
  • Example 2 and Example 3 were included in a 10W30 quality HD (diesel) lubricating oil formulations as the dispersant at 2.5 weight percent active ingredient concentration and the oil was evaluated for diesel dispersancy performance in the Caterpillar 1-H/2 test.
  • the formulation also contained olefin copolymer V.I. improver to provide the 1OW30 viscosity grade, 3.1 wt. % of a mixture of overbased and normal metal phenates, 1.5 weight percent of zinc dialkyl dithiophosphate anti-wear additive, and very small proportions of anti-oxidant (0.3%) and anti-foamant (0.2%).

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
EP82304066A 1981-08-17 1982-08-02 Succinimide dispersant amélioré pour huile lubrifiante Expired EP0072645B1 (fr)

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US293146 1981-08-17

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Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986003987A1 (fr) * 1984-12-27 1986-07-17 The Lubrizol Corporation Sels dispersants
FR2586255A1 (fr) * 1985-08-14 1987-02-20 Inst Francais Du Petrole Compositions ameliorees d'additifs dispersants pour huiles lubrifiantes et leur preparation
EP0264247A2 (fr) * 1986-10-16 1988-04-20 Exxon Chemical Patents Inc. Additifs dispersants à bas poids moléculaire, solubles dans l'huile à haute fonctionnalité, utilisables dans des compositions d'huile
US4803003A (en) * 1987-06-16 1989-02-07 Exxon Chemical Patents Inc. Ethylene copolymer viscosity index improver dispersant additive useful in oil compositions
US4863624A (en) * 1987-09-09 1989-09-05 Exxon Chemical Patents Inc. Dispersant additives mixtures for oleaginous compositions
EP0438848A1 (fr) * 1990-01-25 1991-07-31 Ethyl Petroleum Additives Limited Inhibition de la dégradation des fluoroélastomères durant la lubrification
EP0438847A1 (fr) * 1990-01-25 1991-07-31 Ethyl Petroleum Additives Limited Compositions de succinimide
EP0444830A1 (fr) * 1990-02-26 1991-09-04 Ethyl Petroleum Additives Limited Composition à base de succinimide
EP0532264A2 (fr) * 1991-09-09 1993-03-17 Betz Europe, Inc. Traitement thermique d'une matière liquide hydrocarbonée
US5254669A (en) * 1991-08-30 1993-10-19 Bp Chemicals Limited Crosslinked polymer from long alkyl chain polyamine
US5328624A (en) * 1987-06-16 1994-07-12 Exxon Chemical Patents Inc. Stabilized grafted ethylene copolymer additive useful in oil compositions
US5466387A (en) * 1993-06-16 1995-11-14 Agip Petroli S.P.A. Oil-soluble adducts of disuccinimides and anhydrides of unsaturated bicarboxylic aliphatic acids
EP0776963A1 (fr) * 1995-12-01 1997-06-04 Chevron Chemical Company Polyalkylène succinimides et leur dérivés post-traités
US5716912A (en) * 1996-04-09 1998-02-10 Chevron Chemical Company Polyalkylene succinimides and post-treated derivatives thereof
US6051537A (en) * 1985-07-11 2000-04-18 Exxon Chemical Patents Inc Dispersant additive mixtures for oleaginous compositions
WO2000026327A1 (fr) * 1998-10-30 2000-05-11 The Lubrizol Corporation Dispersant ameliore par traitement a l'anhydride de l'acide maleique
EP1195427A2 (fr) * 2000-09-28 2002-04-10 Nippon Mitsubishi Oil Corporation Compositions lubrifiantes convenant comme huiles moteur

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US4663064A (en) * 1986-03-28 1987-05-05 Texaco Inc. Dibaisic acid lubricating oil dispersant and viton seal additives
CA1327088C (fr) * 1986-12-12 1994-02-15 Malcolm Waddoups Additifs oleosolubles pour compositions oleagineuses
US6140280A (en) * 1996-10-29 2000-10-31 Idemitsu Kosan Co., Ltd. Succinimide compound and method for producing it, lubricating oil additive comprising the compound and lubricating oil composition comprising the compound for diesel engine

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US3415750A (en) * 1963-10-04 1968-12-10 Monsanto Co Imidazolines having polyalkenylsuccinimido-containing substituents
GB1162436A (en) * 1967-03-18 1969-08-27 Orobis Ltd Ashless Dispersants
US3639242A (en) * 1969-12-29 1972-02-01 Lubrizol Corp Lubricating oil or fuel containing sludge-dispersing additive

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US3415750A (en) * 1963-10-04 1968-12-10 Monsanto Co Imidazolines having polyalkenylsuccinimido-containing substituents
GB1162436A (en) * 1967-03-18 1969-08-27 Orobis Ltd Ashless Dispersants
US3639242A (en) * 1969-12-29 1972-02-01 Lubrizol Corp Lubricating oil or fuel containing sludge-dispersing additive

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986003987A1 (fr) * 1984-12-27 1986-07-17 The Lubrizol Corporation Sels dispersants
US6051537A (en) * 1985-07-11 2000-04-18 Exxon Chemical Patents Inc Dispersant additive mixtures for oleaginous compositions
FR2586255A1 (fr) * 1985-08-14 1987-02-20 Inst Francais Du Petrole Compositions ameliorees d'additifs dispersants pour huiles lubrifiantes et leur preparation
EP0213027A1 (fr) * 1985-08-14 1987-03-04 Institut Français du Pétrole Compositions améliorées d'additifs dispersants pour huiles lubrifiantes et leur préparation
US4747964A (en) * 1985-08-14 1988-05-31 Institut Francais Du Petrole Dispersing additive compositions for lubricating oils and their manufacture
EP0264247A2 (fr) * 1986-10-16 1988-04-20 Exxon Chemical Patents Inc. Additifs dispersants à bas poids moléculaire, solubles dans l'huile à haute fonctionnalité, utilisables dans des compositions d'huile
EP0264247A3 (en) * 1986-10-16 1988-10-05 Exxon Chemical Patents Inc. High functionality low molecular weight oil soluble dispersant additive useful in oleaginous compositions
US5756428A (en) * 1986-10-16 1998-05-26 Exxon Chemical Patents Inc. High functionality low molecular weight oil soluble dispersant additives useful in oleaginous composition
US5328624A (en) * 1987-06-16 1994-07-12 Exxon Chemical Patents Inc. Stabilized grafted ethylene copolymer additive useful in oil compositions
US4803003A (en) * 1987-06-16 1989-02-07 Exxon Chemical Patents Inc. Ethylene copolymer viscosity index improver dispersant additive useful in oil compositions
US4863624A (en) * 1987-09-09 1989-09-05 Exxon Chemical Patents Inc. Dispersant additives mixtures for oleaginous compositions
EP0438847A1 (fr) * 1990-01-25 1991-07-31 Ethyl Petroleum Additives Limited Compositions de succinimide
EP0438848A1 (fr) * 1990-01-25 1991-07-31 Ethyl Petroleum Additives Limited Inhibition de la dégradation des fluoroélastomères durant la lubrification
EP0444830A1 (fr) * 1990-02-26 1991-09-04 Ethyl Petroleum Additives Limited Composition à base de succinimide
US5254669A (en) * 1991-08-30 1993-10-19 Bp Chemicals Limited Crosslinked polymer from long alkyl chain polyamine
EP0532264A3 (en) * 1991-09-09 1993-07-21 Betz Europe, Inc. Heat processing of liquid hydrocarbonaceous medium
EP0532264A2 (fr) * 1991-09-09 1993-03-17 Betz Europe, Inc. Traitement thermique d'une matière liquide hydrocarbonée
US5466387A (en) * 1993-06-16 1995-11-14 Agip Petroli S.P.A. Oil-soluble adducts of disuccinimides and anhydrides of unsaturated bicarboxylic aliphatic acids
US5821205A (en) * 1995-12-01 1998-10-13 Chevron Chemical Company Polyalkylene succinimides and post-treated derivatives thereof
US5849676A (en) * 1995-12-01 1998-12-15 Chevron Chemical Company Post-treated derivatives of polyalkylene succinimides
US5851965A (en) * 1995-12-01 1998-12-22 Chevron Chemical Company Dispersant compositions having polyalkylene succinimides
US5853434A (en) * 1995-12-01 1998-12-29 Chevron Chemical Company Fuel compositions having polyalkylene succinimides and preparation thereof
US5872083A (en) * 1995-12-01 1999-02-16 Chevron Chemical Company Post-treated derivatives of polyalkylene succinimides
EP0776963A1 (fr) * 1995-12-01 1997-06-04 Chevron Chemical Company Polyalkylène succinimides et leur dérivés post-traités
US6358892B1 (en) * 1995-12-01 2002-03-19 Chevron Chemical Company Polyalkylene succinimides and post-treated derivatives thereof
US5716912A (en) * 1996-04-09 1998-02-10 Chevron Chemical Company Polyalkylene succinimides and post-treated derivatives thereof
WO2000026327A1 (fr) * 1998-10-30 2000-05-11 The Lubrizol Corporation Dispersant ameliore par traitement a l'anhydride de l'acide maleique
EP1195427A2 (fr) * 2000-09-28 2002-04-10 Nippon Mitsubishi Oil Corporation Compositions lubrifiantes convenant comme huiles moteur
EP1195427A3 (fr) * 2000-09-28 2003-04-09 Nippon Mitsubishi Oil Corporation Compositions lubrifiantes convenant comme huiles moteur

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Publication number Publication date
JPS5838792A (ja) 1983-03-07
CA1190216A (fr) 1985-07-09
EP0072645A3 (en) 1984-09-05
DE3274976D1 (de) 1987-02-12
EP0072645B1 (fr) 1987-01-07
BR8204774A (pt) 1983-08-02
JPH0328477B2 (fr) 1991-04-19

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