US2270241A - Lubricating oil - Google Patents

Lubricating oil Download PDF

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US2270241A
US2270241A US363500A US36350040A US2270241A US 2270241 A US2270241 A US 2270241A US 363500 A US363500 A US 363500A US 36350040 A US36350040 A US 36350040A US 2270241 A US2270241 A US 2270241A
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Prior art keywords
oil
soluble
amount
lubricating oil
salt
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US363500A
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Adams Elmer Wade
Lawrence C Brunstrum
Alfred W Weitkamp
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Standard Oil Co
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Standard Oil Co
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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
    • C10M141/00Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/10Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic phosphorus-containing compound
    • 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
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less 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
    • 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
    • C10M2207/121Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
    • C10M2207/122Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
    • 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
    • C10M2207/10Carboxylix 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
    • 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
    • C10M2207/10Carboxylix 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
    • 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
    • C10M2223/10Phosphatides, e.g. lecithin, cephalin
    • 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
    • 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
    • C10N2010/02Groups 1 or 11
    • 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

Definitions

  • Free fatty acid, certain esters, numerous alcohols, fats, sulfonic soaps, etc. have long been known to exert a solubilizing influence on metallic salts and soaps to a greater or lesser degree.
  • One object of the present invention is to add organic metallic salts and/or soaps which are normally insoluble in oil or at most soluble to a rather small degree to a lubricant together with a new and improved solubilizer.
  • the salt or soap and solubilizer maybe added to the oil separately or together or they may be reacted together and the resulting product added to the oil.
  • the present invention relates to' the use of phosphatides and commercial mixtures of the same as solubilizers for metal salts of aliphatic carboxylic acids and metal soaps of fatty acids which are slightly soluble in oil.
  • Phosphatides include, for example, lecithin and cephalin, while the commercial mixtures comprise mixtures of both lecithin and cephaline together with residual fatty oil and free fatty acids.
  • the commercial products frequently contain about 65% phosphatides, based on phosphorus content and about of fatty oil plus fatty acid.
  • Phosphatides have been found to be far superior to any of the solubilizers mentioned hereinbefore when the addition of slightly oil-soluble metallic salts of carboxylic acids and fatty acid soaps are contemplated.
  • a lubricating oil, to which the addition agent and solubilizer have been added, is clear and transparent.
  • the use of phosphatides or phosphatidic material has the further advantage that the solubilizer itself serves to stabilize the mineral oil. This is particularly advantageous in view of the fact that certain previously known solubilizers, such as fatty acids,
  • the normally slightly oil-soluble salts and soaps which are contemplated in the present invention ar the Group I and Group II metal salts of aliphatic acids, particularly straight-chain carboxylic acids such as stearic, palmitic, ricinoleic, oleic, and the like, and even acids such as formic, acetic, propionic, butyric and the like.
  • the term metal salts" as used in the present specification is intended to include not only those metallic salts of fatty acids which are normally regarded as soaps, but also the metallic salts of the low molecular weight aliphatic acids such as formic, acetic, etc.
  • the present invention relates to such salts as calcium or sodium stearate or palmitate, strontium oleate, cadmium butyrate,
  • the metallic salt or the phosphatide it is possible to add either the metallic salt or the phosphatide to the oil first. It is, furthermore, possible to treat the metallic salt with the phosphatide before adding the reaction mixture to the oil.
  • Calcium salts of essentially saturated fatty acids having 22 to 26 carbon atoms are soluble in mineral oil to the extent of not more than about 0.25% without the use of a solubilizer. Most calcium salts of fatty acids having 20 carbon atoms or less are practically insoluble in mineral oil even at elevated temperatures.
  • the calcium soap or No. 2 Stearine Pitch which contains chains varying in length from 12 to 24 carbon atoms, although fairly soluble in hot oil, gradually separates from the oil at room temperature.
  • phosphatidic materials is suflicient to act as solubilizer for from 0.1% to 1.0% of calcium salts which are normally slightly soluble in mineral oil. More specifically, 1.5% phosphatide will completely solubilize 0.25% of a calcium salt of an aliphatic acid, which is, in most cases the desired quantity of the addition agent. It is to be noted, in accordance with the present invention, that the phosphatidic material may also be used for the purpose of improving the solubility of calcium acetate, barium butyrate,
  • metal salts which are already solublein oil to a greater or lesser degree.
  • a water solution, preferably concentrated, of the desired metal salt, such as cadmium formate and the like is added directly to the commercial phosphatide which has been slightly warmed.
  • the commercial phosphatide may be diluted with mineral oil, preferably in the proportion of 1 part material to 1 part or more of mineral oil.
  • the water is evaporated ofi under reduced pressure.
  • the double salt may then be added in amounts of from 0.05% to 1% or more to the oil. If desired other types of addition agents or inhibitors may be added to the oil.
  • a lubricant comprising a lubricating oil, a metal salt of a carbomrlic acid in an amount in excess of that which would be soluble in said lubricating oil and a phosphatidic material in an amount suflicient to render said first mentioned amount of said salt soluble in said oil.
  • a lubricant as claimed in claim 1 wherein the phosphatidic material comprises lecithin and I cephalin.
  • a lubricant comprising a lubricating oil, a Group I metal salt of an aliphatic acid in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatidic material in an amount sufficient to render said first-mentioned amount of metal salt soluble in said oil.
  • a lubricant comprising a lubricating oil, a Group II metal salt of an aliphatic acid in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatidic material in an amount sufiicient to render said first-mentioned amount of metal salt soluble in said oil.
  • a process for improving a lubricating oil comprising incorporating with said oil a metal salt of an aliphatic acid in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
  • a process for improving a lubricating oil comprising incorporating with said oil a. sodium salt of an aliphatic acid having not more than 26 carbon atoms in an amount in excess of that which would be normally soluble in said lubricating oil. and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
  • a process for improving a lubricating oil comprising incorporating with said oil a calcium salt of an aliphatic acid having not more than 26 carbon atoms in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
  • a process for improving a lubricating oil comprising incorporating with said oil an alkali metal stearate in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
  • a process for improving a lubricating oil comprising incorporating with said oil an alkaline earth metal stearate in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount suflicient to render said first-mentioned amount of salt soluble in said oil.

Description

Patented Jan. 20, 1942 LUBRIOATING OIL Elmer Wade Adams, Hammond, Ind., Lawrence C. Brunstrum, Chicago, Ill., and- Alfred W. Weitkamn, Whiting, Ind assignors to Standard Oil Company, Chicago, 11]., a corporation of Indiana No Drawing. Application October 30, 1940,
Serial No. 363,500
12 Claims.
in order to obtain the full benefits of the addition agent. Free fatty acid, certain esters, numerous alcohols, fats, sulfonic soaps, etc. have long been known to exert a solubilizing influence on metallic salts and soaps to a greater or lesser degree.
One object of the present invention is to add organic metallic salts and/or soaps which are normally insoluble in oil or at most soluble to a rather small degree to a lubricant together with a new and improved solubilizer.
The salt or soap and solubilizer maybe added to the oil separately or together or they may be reacted together and the resulting product added to the oil.
More particularly the present invention relates to' the use of phosphatides and commercial mixtures of the same as solubilizers for metal salts of aliphatic carboxylic acids and metal soaps of fatty acids which are slightly soluble in oil. Phosphatides include, for example, lecithin and cephalin, while the commercial mixtures comprise mixtures of both lecithin and cephaline together with residual fatty oil and free fatty acids. The commercial products frequently contain about 65% phosphatides, based on phosphorus content and about of fatty oil plus fatty acid.
Whenever the term phosphatides appears herein it is to be understood that not only the pure compounds such as lecithin and cephalin but also the commercial mixtures of lecithin, cephalin, oil, etc. are intended.
Phosphatides have been found to be far superior to any of the solubilizers mentioned hereinbefore when the addition of slightly oil-soluble metallic salts of carboxylic acids and fatty acid soaps are contemplated. A lubricating oil, to which the addition agent and solubilizer have been added, is clear and transparent. The use of phosphatides or phosphatidic material has the further advantage that the solubilizer itself serves to stabilize the mineral oil. This is particularly advantageous in view of the fact that certain previously known solubilizers, such as fatty acids,
alcohols, esters, etc. have an adverse effect in this regard.
It is believed that the phosphatidic material reacts with the normally slightly oil-soluble organic salt or soap to form a complex or double salt which is more readily soluble in oil. It is, therefore, a further object of the present invention to provide a method for preparing such complex salts.
The normally slightly oil-soluble salts and soaps which are contemplated in the present invention ar the Group I and Group II metal salts of aliphatic acids, particularly straight-chain carboxylic acids such as stearic, palmitic, ricinoleic, oleic, and the like, and even acids such as formic, acetic, propionic, butyric and the like. The term metal salts" as used in the present specification is intended to include not only those metallic salts of fatty acids which are normally regarded as soaps, but also the metallic salts of the low molecular weight aliphatic acids such as formic, acetic, etc.
More particularly, the present invention relates to such salts as calcium or sodium stearate or palmitate, strontium oleate, cadmium butyrate,
calcium formate, acetate or propionate, copper acetate and the like.
In carrying out the present invention, it is possible to add either the metallic salt or the phosphatide to the oil first. It is, furthermore, possible to treat the metallic salt with the phosphatide before adding the reaction mixture to the oil. Calcium salts of essentially saturated fatty acids having 22 to 26 carbon atoms are soluble in mineral oil to the extent of not more than about 0.25% without the use of a solubilizer. Most calcium salts of fatty acids having 20 carbon atoms or less are practically insoluble in mineral oil even at elevated temperatures. Furthermore, the calcium soap or No. 2 Stearine Pitch which contains chains varying in length from 12 to 24 carbon atoms, although fairly soluble in hot oil, gradually separates from the oil at room temperature.
It has been found that 0.1% to 7.5% of phosphatidic materials is suflicient to act as solubilizer for from 0.1% to 1.0% of calcium salts which are normally slightly soluble in mineral oil. More specifically, 1.5% phosphatide will completely solubilize 0.25% of a calcium salt of an aliphatic acid, which is, in most cases the desired quantity of the addition agent. It is to be noted, in accordance with the present invention, that the phosphatidic material may also be used for the purpose of improving the solubility of calcium acetate, barium butyrate,
metal salts which are already solublein oil to a greater or lesser degree.
It is sometimes advisable to prepare the double salts of the phosphatides before addition to the oil and this may be accomplished in the following manner: A water solution, preferably concentrated, of the desired metal salt, such as cadmium formate and the like is added directly to the commercial phosphatide which has been slightly warmed. If desired, and in order to facilitate handling, the commercial phosphatide may be diluted with mineral oil, preferably in the proportion of 1 part material to 1 part or more of mineral oil. After the reaction has taken place, the water is evaporated ofi under reduced pressure. The double salt may then be added in amounts of from 0.05% to 1% or more to the oil. If desired other types of addition agents or inhibitors may be added to the oil.
While the present invention has been described in connection with certain preferred embodiments, it is to be understood that these are by way of illustration and not by way of limitation. The scope of the present invention is to be limited only by the appended claims.
We claim: a
1. A lubricant comprising a lubricating oil, a metal salt of a carbomrlic acid in an amount in excess of that which would be soluble in said lubricating oil and a phosphatidic material in an amount suflicient to render said first mentioned amount of said salt soluble in said oil.
2. A lubricant as claimed in claim 1 wherein the phosphatidic material comprises lecithin and I cephalin.
in said lubricating oil, and a phosphatidic material in an amount suiiicient to render said firstmentioned amount of metal salt soluble in said oil.
6. A lubricant comprising a lubricating oil, a Group I metal salt of an aliphatic acid in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatidic material in an amount sufficient to render said first-mentioned amount of metal salt soluble in said oil.
"I. A lubricant comprising a lubricating oil, a Group II metal salt of an aliphatic acid in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatidic material in an amount sufiicient to render said first-mentioned amount of metal salt soluble in said oil.
8. A process for improving a lubricating oil comprising incorporating with said oil a metal salt of an aliphatic acid in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
9. A process for improving a lubricating oil comprising incorporating with said oil a. sodium salt of an aliphatic acid having not more than 26 carbon atoms in an amount in excess of that which would be normally soluble in said lubricating oil. and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
10. A process for improving a lubricating oil comprising incorporating with said oil a calcium salt of an aliphatic acid having not more than 26 carbon atoms in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
11. A process for improving a lubricating oil comprising incorporating with said oil an alkali metal stearate in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount sufiicient to render said first-mentioned amount of salt soluble in said oil.
12. A process for improving a lubricating oil comprising incorporating with said oil an alkaline earth metal stearate in an amount in excess of that which would be normally soluble in said lubricating oil, and a phosphatide in an amount suflicient to render said first-mentioned amount of salt soluble in said oil.
ELMER W DE ADAMS. LAWRENC C. BRUNSTRUM. ALFRED W. WEITKAMP CERTIFICATE OF CORRECTION,
Patent No. 2,270,2LL1. January 20, 19t2.
EIMER WADE ADAMS, ET AL.
4 It is hereby'certiiied that error appears in the printed specification of the abovevnumbered patent requiring correction asfollowsz Page 1-, first column, line 52', for "cephaline" read -cephalin-; page 2, first column,
line 50, claim 1, before 'soluole" insert "normallyand that. the said Letters Patent should be read with this correction-therein that the same may conform to the record of the case in the Patent Office.
si neq and sealed this 10th day of" March, A. D. 191m.
7 Henry Van Arsdale, (Seal) Acting Commissioner of Patents.
i DISCLAIMER I 2,270,241.---Elmer Wade Adams, Hammond, Ind., Lawrence 0. Brunstrum, 01m
g0 111., and Alfred W. We'itkamp, Whiting, Ind. LUBRIQATING/ OIL. Patent dated January 20, 1942. Disclaimer filed June 3, 19513, by the assignee, Standard 0il"0ompany, (Indiana). i
Hereby enters this disclaimer to claims 1,2, 3, 4, 5, 7, "8; 1 0, and 12 of the above numbered patent. v
[Ojfieial Gazette June 29, 1943.]
US363500A 1940-10-30 1940-10-30 Lubricating oil Expired - Lifetime US2270241A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3284409A (en) * 1965-06-22 1966-11-08 Lubrizol Corp Substituted succinic acid-boron-alkylene amine phosphatide derived additive and lubricating oil containing same
US4501677A (en) * 1983-11-02 1985-02-26 Exxon Research & Engineering Co. Heterocyclic nitrogen compounds--organometallic salt complexes as corrosion inhibitors in lubricating oils
US5135669A (en) * 1989-03-09 1992-08-04 Exxon Chemical Patents Inc. Hydrogenated lecithin for friction and flow properties
US5487838A (en) * 1991-04-18 1996-01-30 The Lubrizol Corporation Reaction products of a boron compound and a phospholipid, and lubricant and aqueous fluids containing same
US5487839A (en) * 1991-04-18 1996-01-30 The Lubrizol Corporation Grease compositions

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3284409A (en) * 1965-06-22 1966-11-08 Lubrizol Corp Substituted succinic acid-boron-alkylene amine phosphatide derived additive and lubricating oil containing same
US4501677A (en) * 1983-11-02 1985-02-26 Exxon Research & Engineering Co. Heterocyclic nitrogen compounds--organometallic salt complexes as corrosion inhibitors in lubricating oils
US5135669A (en) * 1989-03-09 1992-08-04 Exxon Chemical Patents Inc. Hydrogenated lecithin for friction and flow properties
US5487838A (en) * 1991-04-18 1996-01-30 The Lubrizol Corporation Reaction products of a boron compound and a phospholipid, and lubricant and aqueous fluids containing same
US5487839A (en) * 1991-04-18 1996-01-30 The Lubrizol Corporation Grease compositions

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