US3194813A - High molecular weight alkenyl-n-omega amino hexylsuccinimide - Google Patents

High molecular weight alkenyl-n-omega amino hexylsuccinimide Download PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
oil
compositions
hexylsuccinimide
molecular weight
lubricating
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.)
Expired - Lifetime
Application number
US231554A
Inventor
Suer William M Le
George R Norman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lubrizol Corp
Original Assignee
Lubrizol Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Lubrizol Corp filed Critical Lubrizol Corp
Priority to US231554A priority Critical patent/US3194813A/en
Application granted granted Critical
Publication of US3194813A publication Critical patent/US3194813A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic 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
    • C07D207/30Heterocyclic 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
    • C07D207/34Heterocyclic 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
    • C07D207/36Oxygen or sulfur atoms
    • C07D207/402,5-Pyrrolidine-diones
    • C07D207/4042,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
    • C07D207/408Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms
    • C07D207/412Acyclic radicals containing more than six carbon atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/30Introducing nitrogen atoms or nitrogen-containing groups
    • C08F8/32Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/282Esters of (cyclo)aliphatic oolycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/34Esters having a hydrocarbon substituent of thirty or more carbon atoms, e.g. substituted succinic acid derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/40Fatty vegetable or animal oils
    • C10M2207/404Fatty vegetable or animal oils obtained from genetically modified species
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/086Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/28Amides; Imides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/088Neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C10M2219/087Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
    • C10M2219/089Overbased salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/045Metal containing thio derivatives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/08Resistance to extreme temperature
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/02Bearings
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/12Gas-turbines
    • C10N2040/13Aircraft turbines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/14Electric or magnetic purposes
    • C10N2040/16Dielectric; Insulating oil or insulators
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/14Electric or magnetic purposes
    • C10N2040/17Electric or magnetic purposes for electric contacts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/22Metal 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.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Lubricants (AREA)

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
US231554A 1962-10-18 1962-10-18 High molecular weight alkenyl-n-omega amino hexylsuccinimide Expired - Lifetime US3194813A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US231554A US3194813A (en) 1962-10-18 1962-10-18 High molecular weight alkenyl-n-omega amino hexylsuccinimide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US231554A US3194813A (en) 1962-10-18 1962-10-18 High molecular weight alkenyl-n-omega amino hexylsuccinimide

Publications (1)

Publication Number Publication Date
US3194813A true US3194813A (en) 1965-07-13

Family

ID=22869719

Family Applications (1)

Application Number Title Priority Date Filing Date
US231554A Expired - Lifetime US3194813A (en) 1962-10-18 1962-10-18 High molecular weight alkenyl-n-omega amino hexylsuccinimide

Country Status (1)

Country Link
US (1) US3194813A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US3017416A (en) * 1959-08-28 1962-01-16 Rohm & Haas N-succinimidomethyl-substituted quaternary ammonium compounds
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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Similar Documents

Publication Publication Date Title
US3194812A (en) High molecular weight alkenyl-n-para amino-phenyl succinimide
US3216936A (en) Process of preparing lubricant additives
US3200107A (en) Process for preparing acylated amine-cs2 compositions and products
US3366569A (en) Lubricating compositions containing the reaction product of a substituted succinic acid-producing compound, an amino compound, and an alkenyl cyanide
US2458425A (en) Oil compositions
US3367943A (en) Process for preparing oil soluble additives which comprises reacting a c2 to c5 alkylene oxide with (a) reaction product of an alkenylsuccinic anhydride and an aliphaticpolyamine (b) reaction product of alkenylsuccinic anhydride, a c1 to c30 aliphatic hydrocarbon carboxylic acid and an aliphatic polyamine
USRE26433E (en) Amide and imide derivatives of metal salts of substituted succinic acids
US3018250A (en) Lubricating oil compositions containing nu-dialkylaminoalkyl alkenyl succinimides
US3278550A (en) Reaction products of a hydrocarbonsubstituted succinic acid-producing compound, an amine and an alkenyl cyanide
US3288714A (en) Lubricating oil compositions containing alkenyl succinic anhydrides
US3184474A (en) Reaction product of alkenyl succinic acid or anhydride with polyamine and polyhydricmaterial
US3449250A (en) Dispersency oil additives
US3256185A (en) Lubricant containing acylated aminecarbon disulfide product
JPH0248599B2 (en)
JPS6020439B2 (en) Additives useful in oily compositions
US3451931A (en) Metal-containing detergent-dispersants for lubricants
US3245909A (en) Lubricating composition
US3624115A (en) Coordinated complexes of nitrogenous compounds
US3220949A (en) Lubricating oil compositions containing iodine and ashless nitrogen-containing oil-soluble derivatives of alkenyl succinic anhydride
US3194813A (en) High molecular weight alkenyl-n-omega amino hexylsuccinimide
US3526661A (en) Oil-soluble multifunctional detergent-dispersant comprising an amide of a polyamine and an alkaryl keto acid
US3821302A (en) Olefinic ketone imines and oil compositions containing them
US5310491A (en) Lubricant composition containing antioxidant
US3121059A (en) Compositions of matter having anti-rust properties
US3281357A (en) Process for preparing nitrogen and aluminum containing compositions