US3194813A - High molecular weight alkenyl-n-omega amino hexylsuccinimide - Google Patents
High molecular weight alkenyl-n-omega amino hexylsuccinimide Download PDFInfo
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- US3194813A US3194813A US231554A US23155462A US3194813A US 3194813 A US3194813 A US 3194813A US 231554 A US231554 A US 231554A US 23155462 A US23155462 A US 23155462A US 3194813 A US3194813 A US 3194813A
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
- C07D207/408—Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms
- C07D207/412—Acyclic radicals containing more than six carbon atoms
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/52—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of 30 or more atoms
- C10M133/56—Amides; Imides
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
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- 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
- C10M2207/34—Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
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- 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
- C10M2215/086—Imides
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/28—Amides; Imides
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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
- 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
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
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- 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
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
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- 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
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
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- 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
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/088—Neutral salts
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- 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
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/089—Overbased salts
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- 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
- C10N2030/08—Resistance to extreme temperature
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/02—Bearings
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
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- C—CHEMISTRY; METALLURGY
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
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- 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
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
Definitions
- This invention relates to oil-soluble nitrogen-containing compositions and to the process of preparing the same.
- the compositions of this invention are useful as dispersing agents in lubricants, especially lubricants intended for use in the crankcase of internal combustion engines, gears, and power transmitting units.
- compositions which are adapted for use as additives in hydrocarbon oils.
- a succinimide having the structural formula O RCH N-(0Hz-)sNHz bHz-C ll wherein R is a polyisobutene radical, having from about 50 to about 200 carbon atoms.
- a critical aspect of this invention is that the polyisobutene radical. contains at least about 50 carbon atoms.
- the criticality is predicated upon the discovery that a. similar succiniinide having a smaller R radical in its mo lecular structure is not useful for the purposes of this. invention.
- the sources of the R radical include polyisobutenes having molecular weights within the range from about 7,00 to about 3000.
- Such polymers are well known in the art. They can be obtainedfor instance, by contacting isobutene, preferably in a solvent such as hexane, butane, or naphtha, with, a Friedel-Crafts catalyst such as alumi num chloride, boron trifiuoride, zinc chloride, or titanium tetrachloride at a temperature between about 50 C. and 25 C.
- the polyisobutene-substituted succinimide of this invention is obtained by the reaction of approximately equimolar mixtures of an appropriate polyisobutene-substituted succnic anhydride or acid with hexamethylene diamine.
- the reaction between an anhydride and the diamine is illustrated by the following equation: i
- the reaction should be carried out at a temperature which is sufiiciently high to cause the removal of water from'the, reaction mixture. Ordinarily the temperature isbetween about C. and 250 C., preferably between aboutmolecular weight; The reaction involves merely heating the two reactants at a temperature about 100200 C.
- the product from such a reaction is an alkenyl succinic anhydride, the alkenyl group may be hydrogenated to an alkyl group.
- the anhydride may be hydrolyzed by treatment with water or steam to the corresponding acid.
- Example 1 A polyisobutene-substituted succinic anhydride having an acid number of 97 and an equivalent weight of 577 is prepared by the reaction of a chlorinated polyisobutene (having an average molecular weight of 1000 and a chlorine content of 4.5%) and maleic anhydride. To a mix-v ture of 88 parts (1.1 equivalents or 0.55 mole) of a 72% aqueous solution of hexamethylene diamine and 415 parts of mineral oil, there is added 577 parts (1 equivalent or 0.5 mole) of the polyisobutene-substituted succinic anhydride at 6080 C. within a period of 1 hour. The mixture is heated at 150155 C.
- the principal utility of the polyisobutene-substituted succinimides of this invention is as detergent additives in lubricating oils. They also are useful in other compositions, especially hydrocarbon compositions such as gasolines, burner fuel oils, cutting oils, transformer oils, hydraulic fluids, etc.
- the concentration of the succinimides as additives in such compositions may range from about 0.1% to about by weight.
- lubricating compositions for use. in gasoline internal combustion engines may contain from about 0.5% to about 5% of the additive
- lubricating compositions for use in gears and diesel engines may contain as much as 10% or even more of the additive
- gasolines and burner fuel oils may contain as little as 0.001% or even less of the additive.
- the lubricating oils in which the additive of this invention are useful may be of synthetic, animal, vegetable, or
- oils mineral origin. Ordinarily mineral lubricating oils are preferred by reason of their availability, general excellence, and low cost. For certain applications oils belonging to one of the other three groups may be preferred. For instance, synthetic polyester oils such as didodecyl adipate and di-Z-ethylhexyl sebacate are often preferred as jet engine lubricants. Normally the oils preferred will be fluid oils ranging in viscosity from about 40 Saybolt Universal seconds at 100 F. to about 200 Saybolt Universal seconds at 210 ,F.
- the additive'of this invention may be added to the oil at the appropriate concentration.
- a concentrate of the additive may be prepared by dissolving the additive in a limited amount of the oil and the concentrate may then be diluted with-additional amounts of the oil to prepare the final oil compositions.
- the lubricating compositions in which the additives of this invention are present may contain other additives such as supplemental ashless detergents, metal cont a'ining detergents, corrosion inhibitors, rust inhibitors, oxidation inhibitors, load-carrying additives, anti-foam additives, pour point depressants, viscosity index improving agents,- additives to improve the frictional characteristics,
- additives such as supplemental ashless detergents, metal cont a'ining detergents, corrosion inhibitors, rust inhibitors, oxidation inhibitors, load-carrying additives, anti-foam additives, pour point depressants, viscosity index improving agents,- additives to improve the frictional characteristics
- concentrations of these additives in the lubricating compositions may range from about 0.001% to by weight;
- a specific example of a lubricating composition useful in the crankcase of an automobile is a SAE mineral lubricating oil containing-1.5% (by weight) of the product of Example 1.
- lubricating compo- 5 sitions include: SAE mineral lubricating oil containing 3% of the product of'Exarnple 1 and 1% of zinc dioctylphosphorodithioate; SAE 20 mineral lubricating oil containing 0.5% of the product of Examplel, 1% of barium didodecyl benzene sulfonate, and 2% of 2,6-ditert-butyl-4-methylphenol; and SAE 30 mineral lubricating oil containing 3% of the product of Example 1, 1.5 of his (octylphenyl) sulfide,.and 1% of-dibutyl tetrasultide.
- W at is claimed is: p 1.
- R is a polyiso- 55 butene radical having about 75 carbon atoms.
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Description
United States Patent 3,194,813 HIGH MQLECULAR WEEGHT ALKENYL-N- OfiiEGA AMINO HEXYLSUCClNIh HDE William M. Le Suer, Cleveland, and George R. Norman,
Lyndhurst, Qhio, assignors to The Luhrizol Corporation, vWichliife, Ohio, a corporation of Ohio,
No Drawing. Filed Oct. 18, N62, Ser. No. 231,554
2 Claims. (Cl. 260-6265) This invention relates to oil-soluble nitrogen-containing compositions and to the process of preparing the same. The compositions of this invention are useful as dispersing agents in lubricants, especially lubricants intended for use in the crankcase of internal combustion engines, gears, and power transmitting units.
One of the principal problems associated with presentday crankcase lubricants is that posed by the inevitable presence in the lubricant of foreign particles such as dirt, soot, water and decomposition products resulting from breakdown of the lubricating oil. Even if there were none of this latter contaminant present the very nature of the design of the modern internal combustion engine is such that a significant amount of foreign matter will accumulate in the crankcase. Perhaps the most important of these contaminants is water because it seems to be responsible for the deposition of a mayonnaise-like sludge. It appears that if there were no water present the solid components of the mayonnaise-like sludge would circu late with the oil and be removed by the oil filter. It will be readily appreciated that the deposition of the sludge presents a serious problem with respect to the efficient operation of the engine and that it is desirable to prevent such deposition of sludge-like material.
The presence of water and the precursors of sludge in a lubricating oil is dependent largely upon the operating temperature of the oil. If the oil is operated at a high temperature the waterr, of couse, will be eliminated by evaporation about as fast as it accumulates. In the absence of water as stated above the other foreign particles will be removed by the filter. At low oil temperatures, on the other hand, water will accumulate and so consequently will sludge. It is apparent that the environment in which a crankcase lubricant is maintained will determine to a large extent the ultimate performance of that lubricant.
High operating temperatures are characteristic of a Inbricant in an engine that is run at relatively constant high speed. Thus, in an engine that is run at 60 miles per hour for a long period of time it is very unlikely that there will be any accumulation of water and it is similarly un likely that there will be any formation and deposition of sludge, but in ordinary stop-and-go driving, the crankcase lubricant will be alternately hot and cold, an ideal enviornment for the accumulation of water. In such cases the formation of sludge is a serious problem. This problem has been withv the automotive industry for many years and its solution has been approached by the use of known detergents such as metal phenates and sulfonates but without notable success. Although such known detergents are very effective in solving the detergency problems associated with motor oils at high temperatures they have not been particularly effective in solving the problems associated with low temperature operation, or to put it better, those problems which are associated with crankcase lubricants in engines which are operated at alternating high and low temperatures.
It is accordingly a principal object of this invention to provide novel compositions of matter.
It is also an object of this invention to provide compositions which are adapted for use as additives in hydrocarbon oils.
It is also an object of this invention to provide compo- "ice sitions which are effective as detergents, in lubricating compositions.
It is another object of this invention to provide a novel process for the preparation of products which are effective asdispersants in lubricant compositions.
It is another object of this invention to provide novel compositions which are effective dispersants in lubricant compositions intended. for use in engines operated at alternating high andlow temperatures. 0
It is another object of this invention to provide improved hydrocarbon oil compositions.
It is another object of this invention to provide, improved lubricating compositions.
These and other objects are achieved in accordance with this invention by providing a succinimide having the structural formula O RCH N-(0Hz-)sNHz bHz-C ll wherein R is a polyisobutene radical, having from about 50 to about 200 carbon atoms.
A critical aspect of this invention is that the polyisobutene radical. contains at least about 50 carbon atoms. The criticality is predicated upon the discovery that a. similar succiniinide having a smaller R radical in its mo lecular structure is not useful for the purposes of this. invention.
The sources of the R radical include polyisobutenes having molecular weights within the range from about 7,00 to about 3000. Such polymers are well known in the art. They can be obtainedfor instance, by contacting isobutene, preferably in a solvent such as hexane, butane, or naphtha, with, a Friedel-Crafts catalyst such as alumi num chloride, boron trifiuoride, zinc chloride, or titanium tetrachloride at a temperature between about 50 C. and 25 C.
The polyisobutene-substituted succinimide of this invention is obtained by the reaction of approximately equimolar mixtures of an appropriate polyisobutene-substituted succnic anhydride or acid with hexamethylene diamine. The reaction between an anhydride and the diamine is illustrated by the following equation: i
The reaction should be carried out at a temperature which is sufiiciently high to cause the removal of water from'the, reaction mixture. Ordinarily the temperature isbetween about C. and 250 C., preferably between aboutmolecular weight; The reaction involves merely heating the two reactants at a temperature about 100200 C. The product from such a reaction is an alkenyl succinic anhydride, the alkenyl group may be hydrogenated to an alkyl group. The anhydride may be hydrolyzed by treatment with water or steam to the corresponding acid.
The following example illustrates the preparation of the succinic imides of this invention (parts are by weight):
Example 1 A polyisobutene-substituted succinic anhydride having an acid number of 97 and an equivalent weight of 577 is prepared by the reaction of a chlorinated polyisobutene (having an average molecular weight of 1000 and a chlorine content of 4.5%) and maleic anhydride. To a mix-v ture of 88 parts (1.1 equivalents or 0.55 mole) of a 72% aqueous solution of hexamethylene diamine and 415 parts of mineral oil, there is added 577 parts (1 equivalent or 0.5 mole) of the polyisobutene-substituted succinic anhydride at 6080 C. within a period of 1 hour. The mixture is heated at 150155 C. for 5 hours while nitrogen is bubbled through the mixture. It is then heated to 180 C./20 mm. and filtered. The filtrate is an oil solution containing 40% of the polyisobutene-substituted succinirnide of hexamethylene diamine. The solution is found to have a nitrogen content of 1.4% (the theoretical nitrogen content of the imide is 1.3%). v
The principal utility of the polyisobutene-substituted succinimides of this invention is as detergent additives in lubricating oils. They also are useful in other compositions, especially hydrocarbon compositions such as gasolines, burner fuel oils, cutting oils, transformer oils, hydraulic fluids, etc. The concentration of the succinimides as additives in such compositions may range from about 0.1% to about by weight. For example, lubricating compositions for use. in gasoline internal combustion engines may contain from about 0.5% to about 5% of the additive, lubricating compositions for use in gears and diesel engines may contain as much as 10% or even more of the additive, and gasolines and burner fuel oils may contain as little as 0.001% or even less of the additive.
The lubricating oils in which the additive of this invention are useful may be of synthetic, animal, vegetable, or
mineral origin. Ordinarily mineral lubricating oils are preferred by reason of their availability, general excellence, and low cost. For certain applications oils belonging to one of the other three groups may be preferred. For instance, synthetic polyester oils such as didodecyl adipate and di-Z-ethylhexyl sebacate are often preferred as jet engine lubricants. Normally the oils preferred will be fluid oils ranging in viscosity from about 40 Saybolt Universal seconds at 100 F. to about 200 Saybolt Universal seconds at 210 ,F.
To prepare the final oil compositions the additive'of this invention may be added to the oil at the appropriate concentration. Alternatively, a concentrate of the additive may be prepared by dissolving the additive in a limited amount of the oil and the concentrate may then be diluted with-additional amounts of the oil to prepare the final oil compositions.
The lubricating compositions in which the additives of this invention are present may contain other additives such as supplemental ashless detergents, metal cont a'ining detergents, corrosion inhibitors, rust inhibitors, oxidation inhibitors, load-carrying additives, anti-foam additives, pour point depressants, viscosity index improving agents,- additives to improve the frictional characteristics,
etc. The concentrations of these additives in the lubricating compositions may range from about 0.001% to by weight;
A specific example of a lubricating composition useful in the crankcase of an automobile is a SAE mineral lubricating oil containing-1.5% (by weight) of the product of Example 1. (Ether examples of lubricating compo- 5 sitions include: SAE mineral lubricating oil containing 3% of the product of'Exarnple 1 and 1% of zinc dioctylphosphorodithioate; SAE 20 mineral lubricating oil containing 0.5% of the product of Examplel, 1% of barium didodecyl benzene sulfonate, and 2% of 2,6-ditert-butyl-4-methylphenol; and SAE 30 mineral lubricating oil containing 3% of the product of Example 1, 1.5 of his (octylphenyl) sulfide,.and 1% of-dibutyl tetrasultide.
The effectiveness of the succinimides of this invention as additives in lubricating compositions to prevent the formation of harmful deposits is shown by an oxidationdispersancy test which is useful as a screeningtest for determining the efiectiveness of the additive under light duty service conditions. in this test a' 350cc. sample of a lubricating oil containingtheadditive .is placed in a A 1%x5 /s" SAE 1020 The sample then is heated at 300 F. for 48 hours while air is bubbled through the oil at the rate of 10 liters per hour. The oxidized sample is cooled to F, homogenized with 0.5% by volume of water, allowed to stand at room temperature for 24 hours and then filtered through two layers of No. 1 Whatinan filter paper at 20 mm. mercury pressure. The weight of the precipitate, washed with naphtha and dried, is taken as a measure of the effectiveness of the additive, i.e., the greater the weight of the precipitate the less effective the dispersant additive. By this test a NidContinent, conventionally refined petroleum oil having a viscosity of 200 SayboltUniversal seconds at 100 F. andcontaining 0.001% by weight of iron naphthenatc (to promote oxidation) isfound to give 900-1000 milligrams of sludge per 100 cc. of the oil sample whereas the same oilcontaining additionally 1.5% by weight of the polyisobutene substituted succinimidc of hexamethylene diarnine gives only milligrams of sludge per 100 2" x15" borosilicate tube. steel panel is immersed in (113' oil.
cc. of the oil sample.
W at is claimed is: p 1. A succinimide having the structural formula wherein R is a polyisobutene radical having from about 0 to about 200 carbon atoms.
2. The succinimide of claim 1 wherein R is a polyiso- 55 butene radical having about 75 carbon atoms.
References Cited by the'Exarniner UNITED STATES PATENTS l-llCHOLAS S. RIZZO, Primary Examiner.
: DANIEL E. WYMAN, WALTER A. MODANCE,
' Examiners.
Claims (1)
1. A SUCCINIMIDE HAVING THE STRUCTURAL FORMULA
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US231554A US3194813A (en) | 1962-10-18 | 1962-10-18 | High molecular weight alkenyl-n-omega amino hexylsuccinimide |
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Application Number | Priority Date | Filing Date | Title |
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US231554A US3194813A (en) | 1962-10-18 | 1962-10-18 | High molecular weight alkenyl-n-omega amino hexylsuccinimide |
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US3194813A true US3194813A (en) | 1965-07-13 |
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US231554A Expired - Lifetime US3194813A (en) | 1962-10-18 | 1962-10-18 | High molecular weight alkenyl-n-omega amino hexylsuccinimide |
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US3470197A (en) * | 1967-08-30 | 1969-09-30 | Miles Lab | 1-substituted derivatives of 3-ethyl-4 - (1-methylimidazolyl-(5)-methyl)-2-pyrrolidinone |
WO1992017437A1 (en) * | 1991-03-28 | 1992-10-15 | Bp Chemicals Limited | Poly(1,6-hexanediamine)s and related compounds and their use as lubricating oil additives |
US6440905B1 (en) | 2001-04-24 | 2002-08-27 | The Lubrizol Corporation | Surfactants and dispersants by in-line reaction |
US20100160194A1 (en) * | 2008-12-22 | 2010-06-24 | Chevron Oronite LLC | Post-treated additive composition and method of making the same |
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US3004987A (en) * | 1957-08-15 | 1961-10-17 | Monsanto Chemicals | Acyclic substituted succinic anhydride condensed with diamines |
US3017416A (en) * | 1959-08-28 | 1962-01-16 | Rohm & Haas | N-succinimidomethyl-substituted quaternary ammonium compounds |
US3018291A (en) * | 1959-08-24 | 1962-01-23 | California Research Corp | Nu-dialkylaminoalkyl alkenyl succinimides |
US3024195A (en) * | 1959-08-24 | 1962-03-06 | California Research Corp | Lubricating oil compositions of alkylpiperazine alkenyl succinimides |
US3029250A (en) * | 1959-09-03 | 1962-04-10 | Monsanto Chemicals | Succinimide compounds |
US3087936A (en) * | 1961-08-18 | 1963-04-30 | Lubrizol Corp | Reaction product of an aliphatic olefinpolymer-succinic acid producing compound with an amine and reacting the resulting product with a boron compound |
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US3004987A (en) * | 1957-08-15 | 1961-10-17 | Monsanto Chemicals | Acyclic substituted succinic anhydride condensed with diamines |
US3018291A (en) * | 1959-08-24 | 1962-01-23 | California Research Corp | Nu-dialkylaminoalkyl alkenyl succinimides |
US3018250A (en) * | 1959-08-24 | 1962-01-23 | California Research Corp | Lubricating oil compositions containing nu-dialkylaminoalkyl alkenyl succinimides |
US3024195A (en) * | 1959-08-24 | 1962-03-06 | California Research Corp | Lubricating oil compositions of alkylpiperazine alkenyl succinimides |
US3024237A (en) * | 1959-08-24 | 1962-03-06 | California Research Corp | Alkenyl succinimides of piperazines |
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US3029250A (en) * | 1959-09-03 | 1962-04-10 | Monsanto Chemicals | Succinimide compounds |
US3087936A (en) * | 1961-08-18 | 1963-04-30 | Lubrizol Corp | Reaction product of an aliphatic olefinpolymer-succinic acid producing compound with an amine and reacting the resulting product with a boron compound |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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US3470197A (en) * | 1967-08-30 | 1969-09-30 | Miles Lab | 1-substituted derivatives of 3-ethyl-4 - (1-methylimidazolyl-(5)-methyl)-2-pyrrolidinone |
WO1992017437A1 (en) * | 1991-03-28 | 1992-10-15 | Bp Chemicals Limited | Poly(1,6-hexanediamine)s and related compounds and their use as lubricating oil additives |
US6440905B1 (en) | 2001-04-24 | 2002-08-27 | The Lubrizol Corporation | Surfactants and dispersants by in-line reaction |
US20100160194A1 (en) * | 2008-12-22 | 2010-06-24 | Chevron Oronite LLC | Post-treated additive composition and method of making the same |
EP2379685A2 (en) * | 2008-12-22 | 2011-10-26 | Chevron Oronite Company LLC | A post-treated additive composition and method of making the same |
EP2379685A4 (en) * | 2008-12-22 | 2012-06-20 | Chevron Oronite Co | A post-treated additive composition and method of making the same |
US8859473B2 (en) | 2008-12-22 | 2014-10-14 | Chevron Oronite Company Llc | Post-treated additive composition and method of making the same |
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