US3218264A - Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids - Google Patents

Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids Download PDF

Info

Publication number
US3218264A
US3218264A US147159A US14715961A US3218264A US 3218264 A US3218264 A US 3218264A US 147159 A US147159 A US 147159A US 14715961 A US14715961 A US 14715961A US 3218264 A US3218264 A US 3218264A
Authority
US
United States
Prior art keywords
amine
group
molecular weight
pyrrolidone carboxylic
high molecular
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
US147159A
Inventor
Katz Jacob
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to US147159A priority Critical patent/US3218264A/en
Application granted granted Critical
Publication of US3218264A publication Critical patent/US3218264A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • 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
    • C07D207/18—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 one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22—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 one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24—Oxygen or sulfur atoms
    • C07D207/26—2-Pyrrolidones
    • C07D207/273—2-Pyrrolidones 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 other ring carbon atoms
    • C07D207/277—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • 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
    • C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • 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
    • C10M2215/12—Partial amides of polycarboxylic acids
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/221—Six-membered rings containing nitrogen and carbon only
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/223—Five-membered rings containing nitrogen and carbon only
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/223—Five-membered rings containing nitrogen and carbon only
    • C10M2215/224—Imidazoles
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • 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
    • C10M2215/22—Heterocyclic nitrogen compounds
    • C10M2215/225—Heterocyclic nitrogen compounds the rings containing both nitrogen and oxygen
    • C10M2215/226—Morpholines
    • 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
    • C10M2215/30—Heterocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10—Semi-solids; greasy

Definitions

  • the present invention relates to corrosion inhibition and it particularly relates to corrosion inhibition using pyrrolidone carboxylic amine salts containing long chain fatty groups.
  • the primary object of the present invention is to provide a novel system for corrosion inhibition which involves utilizing long fatty chain substituted pyrrolidone carboxylic acid amine salts which particularly adapt themselves as petroleum additives.
  • a further object is to provide novel amino fatty pyrrolidone carboxylic acid amine salts which are unusually effective as corrosion inhibitors.
  • R represents a high molecular weight group containing from 10 to 30 carbon atoms derived from a high molecular weight primary amine containing amido and amino groups in the long chain; R represents a high molecular weight amine or polyamine containing 10 to 60 carbon atoms.
  • the amine groups in the salt forming molecule may be primary, secondary or tertiary and may be part of an aliphatic structure.
  • R is derived from octadecylamine there will not be an amine group at the end of the long chain R group.
  • the R group is a primary long chain water insoluble aliphatic amine or an aryl alkyl water insoluble amine or a heterocyclic group containing two or three nitrogens having a long aliphatic side chain, said amines and aliphatic side chain containing 10 to 30 carbon atoms;
  • R group may be the radical obtained from such high molecular weight primary amines as follows:
  • Octadecyl amine Primary tallow amine Tertiary-alkyl primary amines Rosin primary amines Dodecylbenzyl amine 1-aminoethyl,2-heptadecyl imidazoline Octadecylaminopropyl amine It will be noted that of the above amines all are primary amines with an amine group at the end of the chain and that the sixth amine terminates in a heterocyclic group and that the last amine has an amino group in the chain as well as a group at the end of the chain. All of these amines are water insoluble.
  • the nitrogen compound which forms the amine salt with the substituted pyrrolidone carboxylic acid should be a high-molecular weight water insoluble amine capable of forming an oil soluble salt of the substituted pyrrolidone carboxylic acid.
  • the substituted pyrrolidone carboxylic acids may be synthesized by reacting high molecular weight Water insoluble primary amines with itaconic acid, its esters or half-esters.
  • this reaction can be made almost quantitive by reacting one mol of a high molecular weight primary amine with one mol of itaconic acid to form the substituted pyrrolidone carboxylic acid, at temperatures ranging from 120 C. to 200 C.
  • This compound is then neutralized with one mol of amine to form the aminesalt, which is readily soluble in most petroleum solvents and hydrocarbons.
  • I-Ieat was applied and'the temperature slowly raised to 200 C. in two hours, during which time one mol of water was r'ecoveredin the moisture trap.
  • This product was neutralized with one mol of l-hydroxyethyl,2-heptadecenyl imidazoline to form an oil soluble compound which was found to have exceptional corrosion inhibiting properties.
  • Example 3 Equimolar portions of dodecylbenzyldiethylenetriamine and dibutyl itaconate was reacted as described in Example 1 and one mol of butyl alcohol was recovered in the Stark-Dean trap.
  • the following table shows theresults obtained by immersing the steel test panels for one minute in the oil under test and properly drained for 20 hours followed by immersion for 20 hours in 500 ml. beakers containing synthetic sea water to a depth of to A3 inch above the panels.
  • the beaker was covered with a watch glass and the temperature of the salt water during the immersion was held at 77 F. After immersion the panels were rinsed with distilled water, acetone and ASTM naphtha in rapid sequence in the order noted and then examined for corrosion and rust spots. 0'
  • the amount of 200 to 1000 partsper million is equivalent to .02. to 0.1%.
  • the critical concentrations are between 200 and 1000 parts per million in which the compounds of Examples 1, 2 and 3 vary from good to excellent.
  • composition of the present application is desirably added to lubricating oils although it may also be used with other hydrocarbon fractions such as gasoline, kerosene, greases and desirably in general in an oleaginous environment.
  • An essential feature of the present invention resides in the fact that polyamines are utilized in the side chains attached to the basic five-membered nitrogen containing heterocyclic ring.
  • the carboxylic acid by itself without the amine salt-forming group attached thereto is much less eifeotive than the pyrrolidone carboxylic acid.
  • a petroleum oil composition consisting essentially of a major proportion of a lubricant petroleum oil and containing a pyrrolidone carboxylic acid amine salt as a corrosion inhibitor in quantities from 200 ppm. to 1,000 ppm, said amine of said amine salt being a high molecular weight primary amine containing 10 to 60 carbon atoms, water-insoluble and capable of forming an oil soluble salt of said acid and being selected from the group consisting of aliphatic amines, alkyl substituted aralkyl amines and hydroxyalkyl substituted alkyl-imidazolines and the pyrollidine ring of said acid having attached to the nitrogen of the ring a high molecular weight group containing from 10 to 30 carbon atoms and being selected from the group consisting of aliphatic radicals, alkyl substituted aralkyl radicals, and alkyl substituted imidazoline radicals.
  • Apetroleum oil composition consisting essentially of a major proportion of a hydrocarbon petroleum lubricating oil and .02 to 0.1% of a pyrrolidone carboxylic acid amine salt of the general formula:
  • a petroleum oil composition consisting essentially of a major proportion of petroleum oil and 200 ppm. to 1,000 ppm. of a pyrrolidone carboxylic acid amine salt as a corrosion inhibitor having the general formula:
  • R is a high molecular weight group containing from 10 to 30 carbon atoms and being selected from the group consisting of aliphatic radicals, alkyl substituted aralkyl radicals, and alkyl substituted imidazoline radicals
  • R is a high molecular weight primary amine containing 10 to 60 carbon atoms which is water-soluble and capable of forming an oil soluble salt of said acid and being selected from the group consisting of aliphatic amines, alkyl substituted aralkyl amines and hydroxyalkyl substituted alkylimidazolines.
  • a petroleum oil composition consisting essentially of a major proportion of petroleum oil and .02% to 0.1% of an oil soluble pyrrolidone carboxylic acid salt of a water insoluble aliphatic amine, said pyrrolidone having attached to the nitrogen of the ring a high molecular weight group containing 10 to 30 carbon atoms and being selected from the group consisting of aliphatic radicals, alkyl substituted aralkyl radicals, and alkyl substituted imidazoline radicals and said aliphatic amine containing 10 to 60 carbon atoms.
  • composition of claim 4 said high molecularv weight group being octadecyl and said amine being tallow aminopropylamine.
  • composition of claim 4 said high molecular weight group being tertiary oetadecyl and said amine being l-hydroxyethyl, Z-heptadecenyl imidazoline.
  • composition of claim 4 said high molecular weight group being dodecylbenzyl and said amine being dimethyl octadecyl amine.
  • a petroleum oil composition consisting essentially of a major amount of petroleum oil and as a corrosion inhibitor from .02% to 0.1% of a pyrrolidone, high molecular Weight aliphatic amine carboxylate of the formula wherein R is a high molecular weight aliphatic primary amine containing to 60 carbon atoms, and R is an aliphatic radical containing 10 to 30 carbon atoms.
  • a petroleum oil composition consisting essentially of a major amount of petroleum oil and from .02% to 0.1% of oil soluble high molecular Weight N-alkyl, 2- pyrrolidone, 4-carboXylic acid salt of a high molecular Weight alkyl amine, said alkyl amine containing 10 to 60 carbon atoms and being Water insoluble, the alkyl radical of said acid having from 10 to carbon atoms.
  • a petroleum oil composition consisting essentially of a major amount of petroleum oil and from .02% to 0.1% of an N-alkyl amino propyl pyrrolidone carboxylic acid salt of a Water insoluble aliphatic amine containing 10 to carbon atoms.

Description

United States Patent 3,218,264 LUBRICANTS CONTAINING AMINE SALTS 0F IAI-CSIIggSTITUTED PYRROLIDONE CARBOXYLIC Jacob Katz, Providence, R1. (48 Hunt, Central Falls, R1.) No Drawing. Filed Oct. 24, 1961, Ser. No. 147,159 Claims. (Cl. 252-336) The present invention relates to corrosion inhibition and it particularly relates to corrosion inhibition using pyrrolidone carboxylic amine salts containing long chain fatty groups.
The primary object of the present invention is to provide a novel system for corrosion inhibition which involves utilizing long fatty chain substituted pyrrolidone carboxylic acid amine salts which particularly adapt themselves as petroleum additives.
A further object is to provide novel amino fatty pyrrolidone carboxylic acid amine salts which are unusually effective as corrosion inhibitors.
These substituted pyrrolidone carboxylic acid amine salts may be characterized by the following formula:
CH CHC O OH.R2
Where R represents a high molecular weight group containing from 10 to 30 carbon atoms derived from a high molecular weight primary amine containing amido and amino groups in the long chain; R represents a high molecular weight amine or polyamine containing 10 to 60 carbon atoms. The amine groups in the salt forming molecule may be primary, secondary or tertiary and may be part of an aliphatic structure.
These compounds have outstanding corrosion inhibiting properties in neutral, basic and acidic oils, lube oils, greases, etc. Where R is derived from octadecylamine there will not be an amine group at the end of the long chain R group.
Essentially the R group is a primary long chain water insoluble aliphatic amine or an aryl alkyl water insoluble amine or a heterocyclic group containing two or three nitrogens having a long aliphatic side chain, said amines and aliphatic side chain containing 10 to 30 carbon atoms;
Thus the R group may be the radical obtained from such high molecular weight primary amines as follows:
Octadecyl amine Primary tallow amine Tertiary-alkyl primary amines Rosin primary amines Dodecylbenzyl amine 1-aminoethyl,2-heptadecyl imidazoline Octadecylaminopropyl amine It will be noted that of the above amines all are primary amines with an amine group at the end of the chain and that the sixth amine terminates in a heterocyclic group and that the last amine has an amino group in the chain as well as a group at the end of the chain. All of these amines are water insoluble.
The nitrogen compound which forms the amine salt with the substituted pyrrolidone carboxylic acid should be a high-molecular weight water insoluble amine capable of forming an oil soluble salt of the substituted pyrrolidone carboxylic acid.
The following are illustrative amines:
Hexadecyl amine Tallow amine Di-hexadecyl amine Dimethyl octadecyl amine Dodecyl benzyl amine Rosin amine 1-hydroxyethyl,Z-heptadecenyl imidazoline Octadecylaminopropyl amine (Duomeen T) t-Octadecylamine (Primene JMT) Oleylaminoethyl piperazine Tallow oxazolines (Alkaterge) the amine forming the salt as set forth in the table above contains amino or amido groups or heterocyclic nitrogen containing rings. The above amines contain 1 to 3 nitrogen atoms. The first three primary amines are preferred in the first group set forth above and the first, second, and fourth amines are preferred in the second group above.
The substituted pyrrolidone carboxylic acids may be synthesized by reacting high molecular weight Water insoluble primary amines with itaconic acid, its esters or half-esters.
Under proper conditions and if necessary, in the presence of certain catalysts, this reaction can be made almost quantitive by reacting one mol of a high molecular weight primary amine with one mol of itaconic acid to form the substituted pyrrolidone carboxylic acid, at temperatures ranging from 120 C. to 200 C.
This compound is then neutralized with one mol of amine to form the aminesalt, which is readily soluble in most petroleum solvents and hydrocarbons.
The following examples are given by way of illustration and are not to beconsidered as limiting the invention in any way.
' Example 1v Equimolar portions of itaconic acid and N-octadecylamine were mixed at C. in a one liter three neck flask equippedwitha Stark-Dean trap, condenser, stirrer and thermometer.
I-Ieat was applied and'the temperature slowly raised to 200 C. in two hours, during which time one mol of water Was r'ecoveredin the moisture trap.
Upon cooling the product set to a hard wax-like solid containing 1-octadecyl,2-pyrrolidone 4-carboxylic acid.
It was soluble in hot isopropyl alcohol and xylene, and insoluble in petroleum ether. The above compound was then melted and neutralized with one mol of tallow aminopropylamine to form an amine salt which was soluble in all proportions in gasoline, kerosene, lubricating Equimolar portions of itaconic acid and t-octadecylamine, known as Primene JMT (Rohm & Haas) were reacted as noted in Example 1 to yield the t-octadecyl pyrrolidone carboxylic acid.
This product was neutralized with one mol of l-hydroxyethyl,2-heptadecenyl imidazoline to form an oil soluble compound which was found to have exceptional corrosion inhibiting properties.
converted into a long chain fatty amine salt;
Example 3 Equimolar portions of dodecylbenzyldiethylenetriamine and dibutyl itaconate was reacted as described in Example 1 and one mol of butyl alcohol was recovered in the Stark-Dean trap.
The resulting butyl ester of the carboxylic acid was hydrolized to form the carboxylic acid. This compound was then neutralized with one mol of dimethyloctadecylamine to form an oil soluble product which had good corrosion inhibiting properties. r
The above substituted pyrrolidone carboxylic acid amine salts were evaluated for their corrosion inhibiting properties as outlined in US. Government military specification MIL-L21260 Lubricating Oil, Internal-Combustion Engine, Preservative. This specification covers preservative engine lubricating oil for use as a lubricant in spark-ignition and compression ignition types of reciprocating internal-combustion engines. The oil used in the test was a light viscosity oil meeting the specifications of Grade 1 in MIL-L-21260 specifications.
Viscosity at 210 F.:
Kinematic, centistokes 5.44 to 7.29
Saybolt Universal, seconds 44 to 50 Pour point, F. max. 20 Flash point, F. min. 360
The following table shows theresults obtained by immersing the steel test panels for one minute in the oil under test and properly drained for 20 hours followed by immersion for 20 hours in 500 ml. beakers containing synthetic sea water to a depth of to A3 inch above the panels.
The beaker was covered with a watch glass and the temperature of the salt water during the immersion was held at 77 F. After immersion the panels were rinsed with distilled water, acetone and ASTM naphtha in rapid sequence in the order noted and then examined for corrosion and rust spots. 0'
F1ailedcorrosion and deep etching.
Gslight c0rrosi0u-edges badly rusted.
Eexcellentno etching, no rust spots, no corrosion.
The amount of 200 to 1000 partsper million is equivalent to .02. to 0.1%. i
The critical concentrations are between 200 and 1000 parts per million in which the compounds of Examples 1, 2 and 3 vary from good to excellent.
This property can not be predicted from the properties of the individual components of the final compounds of Examples 1, 2 and 3 which have very little, if any, corrosive inhibition properties.
These small proportions of 200 to 1000 parts per million are surprisingly effective as compared to the normal proportions of 14% which is used with corrosion inhibitors of the nature of fatty esters, for example sorbitan dioleate.
The unusual property which' results from these com pounds and their high corrosion inhibition qualities appears to result from the interaction of the five-membered nitrogen ring in combination with the long chain amines with the carbon member of the ring adjacent the nitrogen of the ring being doubly-bonded to'oxygen.
It is found necessary to have a carboxylic acid group between the two CH groups in the ring to achieve maximum corrosion inhibition with the carboxylic acid being The composition of the present application is desirably added to lubricating oils although it may also be used with other hydrocarbon fractions such as gasoline, kerosene, greases and desirably in general in an oleaginous environment.
An essential feature of the present invention resides in the fact that polyamines are utilized in the side chains attached to the basic five-membered nitrogen containing heterocyclic ring.
Surprisingly, the carboxylic acid by itself without the amine salt-forming group attached thereto is much less eifeotive than the pyrrolidone carboxylic acid.
Having now particularly described and ascertained the nature of the invention, and in what manner the same is to be performed,
What is claimed is:
1. A petroleum oil composition consisting essentially of a major proportion of a lubricant petroleum oil and containing a pyrrolidone carboxylic acid amine salt as a corrosion inhibitor in quantities from 200 ppm. to 1,000 ppm, said amine of said amine salt being a high molecular weight primary amine containing 10 to 60 carbon atoms, water-insoluble and capable of forming an oil soluble salt of said acid and being selected from the group consisting of aliphatic amines, alkyl substituted aralkyl amines and hydroxyalkyl substituted alkyl-imidazolines and the pyrollidine ring of said acid having attached to the nitrogen of the ring a high molecular weight group containing from 10 to 30 carbon atoms and being selected from the group consisting of aliphatic radicals, alkyl substituted aralkyl radicals, and alkyl substituted imidazoline radicals.
2. Apetroleum oil composition consisting essentially of a major proportion of a hydrocarbon petroleum lubricating oil and .02 to 0.1% of a pyrrolidone carboxylic acid amine salt of the general formula:
CH -CHCOOH.R2
(|JCH3 a where R is a long chain hydrocarbon containing 10 to v30 carbon atoms and R is a water insoluble aliphatic .amine containing 10 to 60 carbon atoms.
' 3. A petroleum oil composition consisting essentially of a major proportion of petroleum oil and 200 ppm. to 1,000 ppm. of a pyrrolidone carboxylic acid amine salt as a corrosion inhibitor having the general formula:
CHg-CHC O OH.R4
Ra-N
where R is a high molecular weight group containing from 10 to 30 carbon atoms and being selected from the group consisting of aliphatic radicals, alkyl substituted aralkyl radicals, and alkyl substituted imidazoline radicals, and R is a high molecular weight primary amine containing 10 to 60 carbon atoms which is water-soluble and capable of forming an oil soluble salt of said acid and being selected from the group consisting of aliphatic amines, alkyl substituted aralkyl amines and hydroxyalkyl substituted alkylimidazolines.
4. A petroleum oil composition consisting essentially of a major proportion of petroleum oil and .02% to 0.1% of an oil soluble pyrrolidone carboxylic acid salt of a water insoluble aliphatic amine, said pyrrolidone having attached to the nitrogen of the ring a high molecular weight group containing 10 to 30 carbon atoms and being selected from the group consisting of aliphatic radicals, alkyl substituted aralkyl radicals, and alkyl substituted imidazoline radicals and said aliphatic amine containing 10 to 60 carbon atoms.
5. The composition of claim 4, said high molecularv weight group being octadecyl and said amine being tallow aminopropylamine.
6. The composition of claim 4, said high molecular weight group being tertiary oetadecyl and said amine being l-hydroxyethyl, Z-heptadecenyl imidazoline.
7. The composition of claim 4, said high molecular weight group being dodecylbenzyl and said amine being dimethyl octadecyl amine.
8. A petroleum oil composition consisting essentially of a major amount of petroleum oil and as a corrosion inhibitor from .02% to 0.1% of a pyrrolidone, high molecular Weight aliphatic amine carboxylate of the formula wherein R is a high molecular weight aliphatic primary amine containing to 60 carbon atoms, and R is an aliphatic radical containing 10 to 30 carbon atoms.
9. A petroleum oil composition consisting essentially of a major amount of petroleum oil and from .02% to 0.1% of oil soluble high molecular Weight N-alkyl, 2- pyrrolidone, 4-carboXylic acid salt of a high molecular Weight alkyl amine, said alkyl amine containing 10 to 60 carbon atoms and being Water insoluble, the alkyl radical of said acid having from 10 to carbon atoms.
10. A petroleum oil composition consisting essentially of a major amount of petroleum oil and from .02% to 0.1% of an N-alkyl amino propyl pyrrolidone carboxylic acid salt of a Water insoluble aliphatic amine containing 10 to carbon atoms.
References Cited by the Examiner UNITED STATES PATENTS 2,363,778 11/1944 Pedersen 4463 2,757,125 7/1956 Mudrak 260-3263 X 2,890,979 6/1959 K-orner 260-326.3 X 2,908,711 10/1959 Halter et al. 252--392 2,945,863 7/1960 Buc et al. 252-392 X DANIEL E. WYMAN, Primary Examiner. JOSEPH R. LIBERMAN, Examiner.

Claims (1)

1. A PETROLEUM OIL COMPOSITION CONSISTING ESSENTIALLY OF A MAJOR PROPORTION OF A LUBRICANT PETROLEUM OIL AND CONTAINING A PYRROLIDONE CARBOXYLIC ACID AMINE SALT AS A CORROSION INHIBITOR IN QUANTITIES FROM 200 P.P.M. TO 1,000 P.M.M., SAID AMINE OF AMINE SALT BEING A HIGH MOLECULAR WEIGHT PRIMARY AMINE CONTAINING 10 TO 60 CARBON ATOMS, WATER-INSOLUBLE AND CAPABLE OF FORMING AN OIL SOLUBLE SALT OF SAID ACID AND BEING SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC AMAINES, ALKYL SUBSTITUTED ARALKYL AMINES AND HYDROXYALKYL SUBSTITUTED ALKYLIMIDAZOLINES AND THE PYRLLIDINE RING OF SAID ACID HAVING ATTACHED TO THE NITROGEN OF THE RING A HIGH MOLECULAR WEIGHT GROUP CONTAINING FROM 10 TO 30 CARBON ATOMS AND BEING SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC RADICALS, ALKYL SUBSTITUTED ARALKYL RADICALS, AND ALKYL SUBSTITUTED IMIDAZOLINE RADICALS.
US147159A 1961-10-24 1961-10-24 Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids Expired - Lifetime US3218264A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US147159A US3218264A (en) 1961-10-24 1961-10-24 Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US147159A US3218264A (en) 1961-10-24 1961-10-24 Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids

Publications (1)

Publication Number Publication Date
US3218264A true US3218264A (en) 1965-11-16

Family

ID=22520499

Family Applications (1)

Application Number Title Priority Date Filing Date
US147159A Expired - Lifetime US3218264A (en) 1961-10-24 1961-10-24 Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids

Country Status (1)

Country Link
US (1) US3218264A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4196091A (en) * 1977-12-27 1980-04-01 Texaco Inc. Lactam carboxylic acids, their method of preparation and use
WO2009086872A1 (en) * 2008-01-10 2009-07-16 Clariant International Ltd Corrosion inhibitors having increased biological degradability and minimized toxicity
DE102008003826A1 (en) 2008-01-10 2009-07-23 Clariant International Limited Corrosion inhibitors with increased biodegradability and reduced toxicity
WO2010149252A1 (en) * 2009-06-25 2010-12-29 Clariant International Ltd Polyalkylene glycol-based ether pyrrolidone carboxylic acids, and concentrates for the production of synthetic cooling lubricants containing the same
DE102009030411A1 (en) 2009-06-25 2010-12-30 Clariant International Limited Water-in-oil emulsion and process for its preparation
WO2013013026A1 (en) * 2011-07-21 2013-01-24 The Lubrizol Corporation Carboxylic pyrrolidinones and methods of use thereof
US20140179574A1 (en) * 2011-07-21 2014-06-26 The Lubrizol Corporation Overbased Friction Modifiers and Methods of Use Thereof
US9068137B2 (en) 2009-06-25 2015-06-30 Clariant Finance (Bvi) Limited Water-mixed metal working fluids containing ether pyrrolidone carboxylic acids
EP2540811B1 (en) * 2008-09-16 2016-06-01 The Lubrizol Corporation Use of heterocyclic compounds for lubricating an internal combustion engine

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2363778A (en) * 1942-12-01 1944-11-28 Du Pont Stabilization of organic substances
US2757125A (en) * 1952-05-16 1956-07-31 Colgate Palmolive Co N-higher alkyl-4-carboxy-2-pyrrolidones and compositions therewith
US2890979A (en) * 1958-01-16 1959-06-16 Procosol Chemical Co Inc Procaine-2-pyrrolidone-5-carboxylate
US2908711A (en) * 1956-06-14 1959-10-13 Gulf Research Development Co Itaconic acid-amine reaction product
US2945863A (en) * 1958-06-24 1960-07-19 Gen Aniline & Film Corp Amides of aminoalkyl pyrrolidones

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2363778A (en) * 1942-12-01 1944-11-28 Du Pont Stabilization of organic substances
US2757125A (en) * 1952-05-16 1956-07-31 Colgate Palmolive Co N-higher alkyl-4-carboxy-2-pyrrolidones and compositions therewith
US2908711A (en) * 1956-06-14 1959-10-13 Gulf Research Development Co Itaconic acid-amine reaction product
US2890979A (en) * 1958-01-16 1959-06-16 Procosol Chemical Co Inc Procaine-2-pyrrolidone-5-carboxylate
US2945863A (en) * 1958-06-24 1960-07-19 Gen Aniline & Film Corp Amides of aminoalkyl pyrrolidones

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4196091A (en) * 1977-12-27 1980-04-01 Texaco Inc. Lactam carboxylic acids, their method of preparation and use
WO2009086872A1 (en) * 2008-01-10 2009-07-16 Clariant International Ltd Corrosion inhibitors having increased biological degradability and minimized toxicity
DE102008003826A1 (en) 2008-01-10 2009-07-23 Clariant International Limited Corrosion inhibitors with increased biodegradability and reduced toxicity
US20100283010A1 (en) * 2008-01-10 2010-11-11 Clariant Finance (Bvi) Limited Corrosion Inhibitors Having Increased Biological Degradability And Minimized Toxicity
US20100283011A1 (en) * 2008-01-10 2010-11-11 Clariant Finance (Bvi) Limited Corrosion Inhibitors Having Increased Biological Degradability And Minimized Toxicity
US8349215B2 (en) 2008-01-10 2013-01-08 Clariant Finance (Bvi) Limited Corrosion inhibitors having increased biological degradability and minimized toxicity
EP2540811B1 (en) * 2008-09-16 2016-06-01 The Lubrizol Corporation Use of heterocyclic compounds for lubricating an internal combustion engine
US9068137B2 (en) 2009-06-25 2015-06-30 Clariant Finance (Bvi) Limited Water-mixed metal working fluids containing ether pyrrolidone carboxylic acids
WO2010149252A1 (en) * 2009-06-25 2010-12-29 Clariant International Ltd Polyalkylene glycol-based ether pyrrolidone carboxylic acids, and concentrates for the production of synthetic cooling lubricants containing the same
DE102009030411A1 (en) 2009-06-25 2010-12-30 Clariant International Limited Water-in-oil emulsion and process for its preparation
WO2013013026A1 (en) * 2011-07-21 2013-01-24 The Lubrizol Corporation Carboxylic pyrrolidinones and methods of use thereof
US20140179574A1 (en) * 2011-07-21 2014-06-26 The Lubrizol Corporation Overbased Friction Modifiers and Methods of Use Thereof
JP2014520891A (en) * 2011-07-21 2014-08-25 ザ ルブリゾル コーポレイション Pyrrolidinone carboxylate and method of use thereof
US20140162920A1 (en) * 2011-07-21 2014-06-12 The Lubrizol Corporation Carboxylic Pyrrolidinones and Methods of Use Thereof
CN103827086B (en) * 2011-07-21 2016-04-13 路博润公司 Carboxylic acid pyrrolidone and using method thereof
CN103827086A (en) * 2011-07-21 2014-05-28 卢布里佐尔公司 Carboxylic pyrrolidinones and methods of use thereof
US9481848B2 (en) * 2011-07-21 2016-11-01 The Lubrizol Corporation Carboxylic pyrrolidinones and methods of use thereof
US9512379B2 (en) * 2011-07-21 2016-12-06 The Lubrizol Corporation Overbased friction modifiers and methods of use thereof

Similar Documents

Publication Publication Date Title
US2699427A (en) Mineral oil compositions containing amidic acids or salts thereof
US3405064A (en) Lubricating oil composition
US4173540A (en) Lubricating oil composition containing a dispersing-varnish inhibiting combination of polyol ester compound and a borated acyl nitrogen compound
US2604451A (en) Mineral oil compositions
US3184474A (en) Reaction product of alkenyl succinic acid or anhydride with polyamine and polyhydricmaterial
US5352377A (en) Carboxylic acid/ester products as multifunctional additives for lubricants
US3251853A (en) Oil-soluble acylated amine
US3429674A (en) Oil-soluble nitrogen composition
US2588412A (en) Mineral oil compositions
US2908711A (en) Itaconic acid-amine reaction product
US3218264A (en) Lubricants containing amine salts of n-substituted pyrrolidone carboxylic acids
US4557846A (en) Lubricating oil compositions containing hydroxamide compounds as friction reducers
US5456731A (en) Carboxylic acid/ester products as multifunctional additives for fuels
US2689828A (en) Mineral oil compositions
US3247110A (en) Fuel oil and lubricating oil compositions containing metal salts of the mono-amidesof tetrapropenyl succinic acid
US3003961A (en) Glycine imides in turbine oil
US3116252A (en) Rust inhibitor for lubricating oil
US2759894A (en) Rust inhibitor
US2605226A (en) Compounded lubricating oil
US2625511A (en) Anticorrosion agents and compositions comprising the same
US3280033A (en) Alkenyl succinamic acids as rust inhibitors and dispersants
US2665995A (en) Rust inhibiting composition
US2742432A (en) Mineral oil lubricating compositions
US3108959A (en) Lubricant additive and composition containing same
US2856299A (en) Water-displacing agent