US2980616A - Soap thickened lubricating grease containing formamide - Google Patents

Soap thickened lubricating grease containing formamide Download PDF

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US2980616A
US2980616A US713541A US71354158A US2980616A US 2980616 A US2980616 A US 2980616A US 713541 A US713541 A US 713541A US 71354158 A US71354158 A US 71354158A US 2980616 A US2980616 A US 2980616A
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grease
formamide
percent
greases
weight
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Edwin C Knowles
Norman R Odell
Joseph F Lyons
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Texaco Inc
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Texaco Inc
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    • 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
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
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    • 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
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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    • 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
    • C10M2207/04Ethers; Acetals; Ortho-esters; Ortho-carbonates
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • C10M2207/128Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids containing hydroxy groups; Ethers thereof
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/281Esters of (cyclo)aliphatic monocarboxylic acids
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    • 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
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/283Esters of polyhydroxy compounds
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/284Esters of aromatic monocarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
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    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/286Esters of polymerised unsaturated acids
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    • 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
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/066Arylene diamines
    • CCHEMISTRY; METALLURGY
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/067Polyaryl amine alkanes
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/08Amides
    • C10M2215/082Amides containing hydroxyl groups; Alkoxylated derivatives
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    • C10M2215/28Amides; Imides
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    • C10N2010/00Metal present as such or in compounds
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/02Groups 1 or 11
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    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
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    • 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
    • C10N2010/06Groups 3 or 13
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention relates to improved lubricating greases. More particularly it relates to soap thickened lubricating greases containing minor'amounts of formamide.
  • the lubricating compositions of this invention comprise essentially a lubricating oil as the chief component containing a fatty acid soap in sufficient amount to thicken the composition to a grease consistency and a minor amount of formamide.
  • the composition may suitably contain about 0.110.0 percent by weight of formamide, and preferably from about 0.5 to about 5.0 percent by weight of formamide based on the Weight of the com position.
  • The'fatty acid soap may be present in widely varying amounts, such as from about 5 to about 45 percent by weight, based on the weight of the composition, and ordinarily in amounts from about 7 to about 30 percent by weight of the grease composition.
  • additives of various types commonly employed in lubricating greases such as other rust inhibitors, oxidation inhibitors, extreme pressure agents, etc.
  • Suitable additives include particularly amines of various types, such as diphenylamine, aplhaand beta-naphthylamines, diphenyl para-phenylene-diamine and tetramethyl diamino diphenyl methane.
  • the fatty acid soaps employed'in these greases may be any of those in general which have been employed as thickening agents in lubricating greases, wherein the metal component may be an alkali metal, an alkaline earth metal or other polyvalent metal such as aluminum,-
  • the fatty acid materials may be naturally occurring orderived from naturally occurring materials, or they may be obtained synthetically, as for example by the oxidation of petroleum fractions.
  • the preferred saponifiable materials are those which comprise at least a major portion of fatty acids containing from about 14 to about 22 carbon atoms per molecule, such as for example, myristic acid, palmitic acid, stearic acid, Oleic acid, tallow fatty acids, 12-hydroxystearic acid, 9,10.- ⁇ dihydroxystearic acid, behenic acid, etc., or the glycerides or other esters of such acids.
  • the lubricating oil component of these greases may be any suitable oils of lubricating characteristics, which may be of mineral, vegetable, animal or synthetic origin, such as have been employed heretofore in lubricating greases.
  • suitable mineral oils include .both distillate and residual fractions from parafiinic, naphthenic or mixed base crudes, ranging from fairly low to fairly high viscosities, such as from about 80 seconds Saybolt Universal at 100 F. to about 220 seconds Saybolt Universal at 210 F.
  • These oils may be obtained by any of the usual refining methods such as acid treating, solvent extraction, and so forth.
  • various synthetic oils may be employed with advantage.
  • suitable oils .of this type may be mentioned high molecular weight aliphatic others, such as normal lubricating oil and preformed soap or by saponification in situ of .the saponifiable material in a portion of the lubricating oil component of the grease.
  • the formamide may be added during the grease preparation when the temperature of the mixture -is below about 200 F., or it may be mixed into thefinished grease.
  • a preferred embodiment of this invention is found in the manufacture of calcium base greases, wherein formamide is particularly effective as a rust inhibitor.
  • a grease was prepared comprising a. mineral lubricating oil containing 14.5 percent by Weight of cal- .cium soap and 1.0 percent by Weight of formamide.
  • the saponifiable materials employed in the preparation of the soaps may be any of those of the usual types, comprising higher fatty acids, containing at least 12 carbon atoms per molecule, which may. be saturated, unsaturated or hydroxy substituted fatty acids, the glychaving a Saybolt Universal viscosity'at F. of about -310 seconds.
  • the saponifiable material Was StarTalloW, having a saponification number: of 197, a neutralization number of 21.6, a' titer, C., of 43.4 and an iodine number of 49.
  • the preparation was carried out by the method comprising saponification in situ in the presence of about /3 of the mineral oil contained in the grease, at about 190 F., dehydration at 300 F., and addition of the remainder of the mineral lubricating oil during cooling. A small amount of water, equivalent to 1 percent by weight of the grease was also added when the grease was at a temperature below about 200 F.
  • the formamide was added by mixing it into the finished grease at room temperature, then reheating the grease to F. and maintaining it at that temperature for 30 minutes with stirring.
  • the following table shows the rust inhibiting and other properties of this grease in comparison with those of the base grease containing no formamide.
  • the water Washing and rusting test comprises essentially rotating a standard X-469 Timken roller bearing packed with a sample of the test grease alternately in air and in water.
  • the weighed bearing packed with 18 grams of the test grease is first rotated in air at room temperature for 30 minutes at 500 r.p.m. in order to uniformly coat the bearing surface with the grease-
  • the bearing trough is then filled with water, which results in the bearing being about 33 percent immersed, and the bearing is rotated for 2 hours at- 500 rpm. while the temperature is maintained 'at 6070 F.
  • the water is then'drained from the trough and the bearing rotated in air for one hour, and again in water for two hours at 6070 F.
  • the bearing is then drained and stored in a humidity cabinet for 7 days, after which it is weighed and inspected to determine the grease loss and the amount of rusting.
  • the calcium soap grease containing 1 percent of formamide prevented any rusting under the severe conditions of this test, Whereas heavy rusting of the bearing occurred with the uninhibited grease.
  • a grease was prepared comprising a mineral lubricating oil containing 7.6 percent by weight of lithium 12-hydroxy stearate and 5.0 percent by Weight of iformamide.
  • the mineral lubricating oil was a blend in about a 6:1 ratio respectively of a refined parafiinic distillate oil having a Saybolt Universal viscosity at 100 .F. of about 182 seconds and a refined Manvel residuum having a Saybolt Universal viscosityat 210 F. of about 92 seconds.
  • the saponifiable material was the methyl ester of 12-hydroxy stearic acid, sold under the trade name of Paricin 1.
  • the preparation was carried out by saponification in situ, employing a small excess of lithium hydroxide, sufficient to give about 0.2 percent of free alkali to the finished grease.
  • the saponification was carried out at about 200 F., and the dehydration at about 300 F.
  • the formamide was added to the grease mixture at room temperature and the mixture then heated to 150 F. and stirred for 30 minutes at that temperature.
  • the following table shows the properties of this grease in comparison to those of the base grease without the inhibitor.
  • a lubricating grease consisting essentially of a mineral lubricating oil thickened to a grease consistency with about 730 percent by weight of a lithium hydroxy fatty acid soap and containing formarnide in an amount from above 1 percent to about 10 percent by Weight, sufficient to impart rust preventiveness to the said grease in the water washing and rusting test.
  • a lubricating grease consisting essentially of a mineral lubricating oil thickened to a grease consistency with about 730 percentby weight of lithium 12-hydroxystearate and containing about 5 percent by weight of formamide, sufiicient to impart rust preventiveness to the said grease in the water washing and rusting test.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

United States Patent SOAP THICKENED LUBRICATING GREASE CONTAINING FORMAMIDE Edwin C. Knowles, Poughkeepsie, Norman R. Odell,
Fishkill, and Joseph F. Lyons, Poughkeepsie, N.Y., assignors to Texaco Inc., a corporation of Delaware No Drawing. Filed Feb 6, 1958, Ser. No. 713,541
2 Claims. (Cl. 252-421) This invention relates to improved lubricating greases. More particularly it relates to soap thickened lubricating greases containing minor'amounts of formamide.
We have found that very superior rust preventive properties and other advantages are obtained by employing small amounts of formamide in soap thickened greases. The rust preventive action of formamide in soap thickened greases is a different result from that obtained with lubricating compositions of other types, such as, for example, water based cutting fluids, wherein formamide has little or no rust preventive action.
The lubricating compositions of this invention comprise essentially a lubricating oil as the chief component containing a fatty acid soap in sufficient amount to thicken the composition to a grease consistency and a minor amount of formamide. The composition may suitably contain about 0.110.0 percent by weight of formamide, and preferably from about 0.5 to about 5.0 percent by weight of formamide based on the Weight of the com position. The'fatty acid soap may be present in widely varying amounts, such as from about 5 to about 45 percent by weight, based on the weight of the composition, and ordinarily in amounts from about 7 to about 30 percent by weight of the grease composition. In addition to the formamide, other additives of various types commonly employed in lubricating greases, such as other rust inhibitors, oxidation inhibitors, extreme pressure agents, etc., may be present in these greases, insofar as no antagonistic effect with the formamide is produced. Suitable additives include particularly amines of various types, such as diphenylamine, aplhaand beta-naphthylamines, diphenyl para-phenylene-diamine and tetramethyl diamino diphenyl methane.
The fatty acid soaps employed'in these greases may be any of those in general which have been employed as thickening agents in lubricating greases, wherein the metal component may be an alkali metal, an alkaline earth metal or other polyvalent metal such as aluminum,-
Patented Apr. 18, 1961 erides or other esters of such acids or mixtures of the free fatty acids and their glycerides or other esters. The fatty acid materials may be naturally occurring orderived from naturally occurring materials, or they may be obtained synthetically, as for example by the oxidation of petroleum fractions. The preferred saponifiable materials are those which comprise at least a major portion of fatty acids containing from about 14 to about 22 carbon atoms per molecule, such as for example, myristic acid, palmitic acid, stearic acid, Oleic acid, tallow fatty acids, 12-hydroxystearic acid, 9,10.-\dihydroxystearic acid, behenic acid, etc., or the glycerides or other esters of such acids.
The lubricating oil component of these greases may be any suitable oils of lubricating characteristics, which may be of mineral, vegetable, animal or synthetic origin, such as have been employed heretofore in lubricating greases. Suitable mineral oils include .both distillate and residual fractions from parafiinic, naphthenic or mixed base crudes, ranging from fairly low to fairly high viscosities, such as from about 80 seconds Saybolt Universal at 100 F. to about 220 seconds Saybolt Universal at 210 F. These oilsmay be obtained by any of the usual refining methods such as acid treating, solvent extraction, and so forth. For certain purposes, such as, for example, the production of low temperature greases, various synthetic oils may be employed with advantage. As ex amples of suitable oils .of this type may be mentioned high molecular weight aliphatic others, such as normal lubricating oil and preformed soap or by saponification in situ of .the saponifiable material in a portion of the lubricating oil component of the grease. The formamide may be added during the grease preparation when the temperature of the mixture -is below about 200 F., or it may be mixed into thefinished grease.
A preferred embodiment of this invention is found in the manufacture of calcium base greases, wherein formamide is particularly effective as a rust inhibitor. As an example of this preferred embodiment of our invention, a grease was prepared comprising a. mineral lubricating oil containing 14.5 percent by Weight of cal- .cium soap and 1.0 percent by Weight of formamide. The
' mineral oil was a refined naphthene base distillate oil copper, cobalt, nickel, etc. The preferred soaps arethose wherein the metalcomponent is an alkali metal or an alkaline earth metal. It is not intended to imply that greases thickened with the different metal soaps are affected in exactly the same manner by the addition of formamide, since in addition to the rust preventive property which formamide imparts to fatty acid soaps generally, its effect otherwise is not necessarily the same, and special advantages are obtained in accordance with this invention with greases of certain types as will hereinafter appear.
The saponifiable materials employed in the preparation of the soaps may be any of those of the usual types, comprising higher fatty acids, containing at least 12 carbon atoms per molecule, which may. be saturated, unsaturated or hydroxy substituted fatty acids, the glychaving a Saybolt Universal viscosity'at F. of about -310 seconds. The saponifiable material Was StarTalloW, having a saponification number: of 197, a neutralization number of 21.6, a' titer, C., of 43.4 and an iodine number of 49. The preparation was carried out by the method comprising saponification in situ in the presence of about /3 of the mineral oil contained in the grease, at about 190 F., dehydration at 300 F., and addition of the remainder of the mineral lubricating oil during cooling. A small amount of water, equivalent to 1 percent by weight of the grease was also added when the grease was at a temperature below about 200 F. The formamidewas added by mixing it into the finished grease at room temperature, then reheating the grease to F. and maintaining it at that temperature for 30 minutes with stirring. The following table shows the rust inhibiting and other properties of this grease in comparison with those of the base grease containing no formamide.
The water Washing and rusting test comprises essentially rotating a standard X-469 Timken roller bearing packed with a sample of the test grease alternately in air and in water. The weighed bearing packed with 18 grams of the test grease is first rotated in air at room temperature for 30 minutes at 500 r.p.m. in order to uniformly coat the bearing surface with the grease- The bearing trough is then filled with water, which results in the bearing being about 33 percent immersed, and the bearing is rotated for 2 hours at- 500 rpm. while the temperature is maintained 'at 6070 F. The water is then'drained from the trough and the bearing rotated in air for one hour, and again in water for two hours at 6070 F. The bearing is then drained and stored in a humidity cabinet for 7 days, after which it is weighed and inspected to determine the grease loss and the amount of rusting. As shown by the above table, the calcium soap grease containing 1 percent of formamide prevented any rusting under the severe conditions of this test, Whereas heavy rusting of the bearing occurred with the uninhibited grease.
Other greases wherein a special advantage is obtained by the addition of minor amounts of formamide are greases thickened with lithium soaps of hydroxy fatty acids. We have found that in these greases the formamide acts as both a rust preventive agent and an oxidation inhibitor, so that lithium hydroxy fatty acid soap greases having both excellent rust inhibiting and antioxidant properties are obtained with the use of a single inhibitor.
As an example of a grease of the above type, a grease was prepared comprising a mineral lubricating oil containing 7.6 percent by weight of lithium 12-hydroxy stearate and 5.0 percent by Weight of iformamide. The mineral lubricating oil was a blend in about a 6:1 ratio respectively of a refined parafiinic distillate oil having a Saybolt Universal viscosity at 100 .F. of about 182 seconds and a refined Manvel residuum having a Saybolt Universal viscosityat 210 F. of about 92 seconds. The saponifiable material was the methyl ester of 12-hydroxy stearic acid, sold under the trade name of Paricin 1. The preparation was carried out by saponification in situ, employing a small excess of lithium hydroxide, sufficient to give about 0.2 percent of free alkali to the finished grease. The saponification was carried out at about 200 F., and the dehydration at about 300 F. The formamide was added to the grease mixture at room temperature and the mixture then heated to 150 F. and stirred for 30 minutes at that temperature. The following table shows the properties of this grease in comparison to those of the base grease without the inhibitor.
Table II Base Containing Grease Grease 5.0% Formamide Penetration at 77 F. ASTM:
Unworked 267 339 Worked (60 strokes). 263 339 Dropping Point, F 383 337 ASTM Bomb Oxidation Test hrs.), 1b.
pressure dropJ 88; 91 4; 5 Water Washing and Rusti Test:
Condition of bearing Heavy N o Rust Rust Condition of grease Poor Good Grease washed from bearing, percent 45 28 As shown by the above table, formamide imparted both a high degree of oxidation resistance and rust preventiveness to the lithium 12-hydroxystearate grease. Smaller amounts of formamide, such as about 1 percent by weight, imparted equivalent oxidation resistance to these greases but generally reduced rust preventiveness.
Such smaller amounts are advantageously employedwhere the softening effect and reductionin dropping point resulting from the addition of formamide to these greases are objectionable, and a high degree of rust preventiveness is not required. However, the softening efiect obtained in these greases on the basis of both unworked and worked penetration is desirable in some cases, where it is desired to obtain greases of a certain grade containing higher amounts of soap.
Obviously many modifications and variations of the invention, as hereinbefore set forth, may be made without departing from the spirit and scope thereof and only such limitations should be imposed as are indicated in the appended claims.
We claim:
1. A lubricating grease consisting essentially of a mineral lubricating oil thickened to a grease consistency with about 730 percent by weight of a lithium hydroxy fatty acid soap and containing formarnide in an amount from above 1 percent to about 10 percent by Weight, sufficient to impart rust preventiveness to the said grease in the water washing and rusting test.
2. A lubricating grease consisting essentially of a mineral lubricating oil thickened to a grease consistency with about 730 percentby weight of lithium 12-hydroxystearate and containing about 5 percent by weight of formamide, sufiicient to impart rust preventiveness to the said grease in the water washing and rusting test.
References Cited in the file of this patent UNITED STATES PATENTS 2,423,343 Plueddemann et a1 July 1, 1941 2,682,508 Godfrey June 29, 1954 FOREIGN PATENTS 988,922 France Sept. 3,1951 735,711 Great Britain Aug. 24, 1955

Claims (1)

1. A LUBRICATING GREASE CONSISTING ESSENTIALLY OF A MINERAL LUBRICATING OIL THICKENED TO A GREASE CONSISTENCY WITH ABOUT 7-30 PERCENT BY WEIGHT OF A LITHIUM HYDROXY FATTY ACID SOAP AND CONTAINING FORMAMIDE IN AN AMOUNT FROM ABOVE 1 PERCENT TO ABOUT 10 PERCENT BY WEIGHT, SUFFICIENT TO IMPART RUST PREVENTIVENESS TO THE SAID GREASE IN THE WATER WASHING AND RUSTING TEST.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3216939A (en) * 1962-06-18 1965-11-09 Universal Oil Prod Co Stabilization of lubricants
CN107406800A (en) * 2015-03-09 2017-11-28 Jxtg能源株式会社 Lubricant composition

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423343A (en) * 1945-04-27 1947-07-01 Westvaco Chlorine Products Cor Process of degreasing aluminum and magnesium surfaces
FR988922A (en) * 1944-01-31 1951-09-03 Lubricant improvements
US2682508A (en) * 1951-05-08 1954-06-29 Monsanto Chemicals Mineral oil compositions of suppressed foaming tendency
GB735711A (en) * 1951-12-15 1955-08-24 Standard Oil Dev Co Improvements in or relating to lubricating compositions

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR988922A (en) * 1944-01-31 1951-09-03 Lubricant improvements
US2423343A (en) * 1945-04-27 1947-07-01 Westvaco Chlorine Products Cor Process of degreasing aluminum and magnesium surfaces
US2682508A (en) * 1951-05-08 1954-06-29 Monsanto Chemicals Mineral oil compositions of suppressed foaming tendency
GB735711A (en) * 1951-12-15 1955-08-24 Standard Oil Dev Co Improvements in or relating to lubricating compositions

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3216939A (en) * 1962-06-18 1965-11-09 Universal Oil Prod Co Stabilization of lubricants
CN107406800A (en) * 2015-03-09 2017-11-28 Jxtg能源株式会社 Lubricant composition
EP3269794A4 (en) * 2015-03-09 2018-08-01 JXTG Nippon Oil & Energy Corporation Grease composition
CN107406800B (en) * 2015-03-09 2021-06-01 Jxtg能源株式会社 Grease composition

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