US2413852A - Rust-inhibiting lubricant - Google Patents

Rust-inhibiting lubricant Download PDF

Info

Publication number
US2413852A
US2413852A US551997A US55199744A US2413852A US 2413852 A US2413852 A US 2413852A US 551997 A US551997 A US 551997A US 55199744 A US55199744 A US 55199744A US 2413852 A US2413852 A US 2413852A
Authority
US
United States
Prior art keywords
oil
reaction product
rust
lubricant
inhibiting
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
US551997A
Inventor
William R Turner
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.)
ATLANTIE REFINING Co
Original Assignee
ATLANTIE REFINING Co
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 ATLANTIE REFINING Co filed Critical ATLANTIE REFINING Co
Priority to US551997A priority Critical patent/US2413852A/en
Application granted granted Critical
Publication of US2413852A publication Critical patent/US2413852A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/04Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • C10M2215/065Phenyl-Naphthyl amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/26Amines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/043Ammonium or amine salts thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/042Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/044Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/135Steam engines or turbines
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/30Refrigerators lubricants or compressors lubricants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/32Wires, ropes or cables lubricants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/34Lubricating-sealants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/36Release agents or mold release agents
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/38Conveyors or chain belts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/40Generators or electric motors in oil or gas winning field
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/42Flashing oils or marking oils
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/44Super vacuum or supercritical use
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/50Medical uses

Definitions

  • the present invention relates to lubricant compositions, and more particularly to rust-inhibiting lubricants suitable for the lubrication of steam turbines, internal combustion engines, gears, cables, and other metal surfaces exposed to rusting or corroding conditions during use.
  • the lubricant of the present invention is especially adapted for use in the lubrication of steam turbines, and has proved very satisfactory in inhibiting rust and corrosion of turbine parts, such rusting normally being caused by the steam condensate entrained in the lubricants heretofore employed.
  • the lubricant of the present invention is not only satisfactory from the view point of rustinhibition, but is likewise substantially unafiected by steam or water and retains a gooddemulsibility value during its use in steam turbines.
  • a hydrocarbon oil such as lubricating oil of suitable viscosity
  • Such reaction product is preferably pnepared by bringing equimolar quantities of thereactants to a temperature between 100 F. and 200 F. and efiecting reaction between the components at such temperature. It is believed, although not definitely known, that the reaction produces an addition salt since no byproducts appear to b formed. The reaction.
  • reaction product usually comprises a clear, reddish-brown, viscous oil. It is not necessary in all cases to use exactly euuimolar proportions of the acid phosphate and the amine, since it has been found desirable to have the reaction product slightly on the alkaline side, with a pH of about 8. This is accomplished by employing a slight excess of the amine over that required for complete neutralization of the acid phosphate. While it is preferred to cause direct reaction between the amine and the acid phosphate, such reaction may be carried out by adding the reactants to hydrocarbon oil, and then adjusting the. temperature of the mixture to effect reaction,
  • the alkyl acid phosphates which may be utilined in making up the reaction product are the monoor dialwl acid phosphates having from 8 to 16 carbon atoms in the alkyl group.
  • monoand diesters, or ixtures thereoh may be I exemplified by the monoand diphosphoridacld esters of octyl alcohol, .nonyl alcohol, tetradecyl alcohol,
  • the alcohols employed in the manufacture of the esters may besingle alcohols or mixtures of such-alcohols of from 8 to lfi-carbon atoms, the alcohols having either s. straightchain or a branched-chain structure.
  • the branched-chain alkylamines containing from 4 to 1! carbon atomsjwhich may be used in the production-of the reaction product includeprimary, secondary, and tertiary amines, or mixtures of two or more thereof.- Exemplary of these compounds, all of which are characterized by the presence of branched-chain alkyl groups,
  • any alkylamine having a carbon chain of 4; to 10 carbon atoms and at least-one substituent alkyl group of 1 to 4 carbons, constituting in into a branched-chain alkylamine, may be employed.
  • an antioxidant suitable for inhibiting the development of acidity or of sludge in the oil.
  • Various amines or phenolic compounds may be employed. preferably a naphthylamine such as phenyl alpha naphthylamine, although other amines compatible with the rust inhibitor may be used.
  • the quantity of'rust inhibiting reaction product to be added to the lubricant is usually small and falls within the range of 0.005% to 1%, the we ferred amount being from 0.01% to 0.1% by weight.
  • the antioxidant which may be utilized 0 in conjunction with the rust inhibitor has been found satisfactory in amounts ranging ,from
  • the present invention may be further illus- I trated by the following example, which. however. is not to be construed as limiting the scope thereof.
  • the acid esters may be Blank oil"...
  • the mixture was added di-Z-ethyl hexylamine, the temperature or the mixture being adjusted to about 130 F.
  • the mixture was thoroughly agitated and during the ensuing reaction, the temperature rose to about 200 F.
  • the quantity of amine added was suflicient to bring the pH of the reaction product to about 8, and in the case of these specific reactants, it was found that 1.1 parts by weight of the lauryl acid phosphate required 1 part by weight of di-2-ethyl hexylamine to produce the desired product of pH8, 'the amine being present in slight excess of that required for complete neutralization.
  • the resulting reaction product which appeared to be an addition salt, consisted of a clear, reddish-brown, viscous oil.
  • This material was added in various percentages, with and without an antioxidant, i. e., phenyl alphanaphthylamine, to a selective solvent refined lubricating oil having an A. P. I. gravityof 32 and a Saybolt universal viscosity of 155 seconds at 100 F.
  • the blank oil and the blends were then tested for rust inhibiting properties in accordance with the A. S. T. M. Method D 665-42T entitled Method of Test for Rust Preventing Characteristics of Steam Turbine Oils in the Presence of Water.
  • Such test comprised essentially immersing a polished steel strip in a beaker containing 300 cc. of oil to be tested, raising the temperature of the oil to 140 F. and stirring for /2 hour, removing 50 cc. of the oil and replacing with 30 cc. of water, continuing the 4 effective for the designated purpose, does not increase the steam emulsion number or the neutralization number beyond permissible limits.
  • lubricants of this invention while especially adapted to the lubrication of steam turbines, are alsosuitable for use in many other mechanisms including internal combustion engines, compressors, gears, and the like.
  • a lubricant comprising hydrocarbon oil and a rust-inhibiting quantity of an oil-soluble reaction product 01 an alkyl acid phosphate having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing from 4 to 16 carbon atoms in the alkyl group.
  • a lubricant comprising hydrocarbon oil, a rust-inhibiting quantity of an oil-soluble reaction product 01 an alkyl acid phosphate having from 8'-to 16 carbon atoms in the alkyl group and a branched-chain alkylamin'e containing i'rom 4 to 16 carbon atoms in the alkyl group, and air amine antioxidant.
  • a lubricant comprising hydrocarbon oil and i from 0.005% to 1.0% by weight or an oil-soluble stirring at 140 F. for 48 hours, removing the steel strip and washing it with naphtha to remove oil, and examining the strip for the percent surface rusted.
  • the reaction product is compatible with the oxidation inhibitor, and its rust inhibiting qualities are not destroyed by the washing action of water. Furthermore the presence of the inhibitor, with or without the antioxidant, in the concentrations reaction product of an alkyl acid phosphate having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing from 4 to 16 carbon atoms in the alkylgroup.
  • a lubricant comprising hydrocarbon .oil, from 0.005% to 1.0% by weight of an oil-soluble reaction product of an alkyl acid phosphate having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing 1mm 4 to 16 carbon atoms in the alkyl group, and from 0.05% to 0.5% by weight of an amine antioxidant.
  • a lubricant comprising hydrocarbon oil and a rust-inhibiting quantity of an oil-soluble reaction product of lauryl acid phosphate and (11-2- ethyl hexylamine.
  • a lubricant comprising hydrocarbon oil, a rust-inhibiting quantity or an oil-soluble reaction product of lauryl acid phosphate and di-2-ethyl hexylamine, and an oxidation-inhibiting quantity of a naphthylamine.
  • a lubricant comprising hydrocarbon oil, from 0.005% to 1.0% by weight of an oil-soluble reaction product oi. lauryl acid,phosphate and di-2-ethyl hexylamine, and irom 0.05% to 0.5% by weight of phenyl alpha naphthylamine.
  • a lubricant comprising hydrocarbon oil, about 0.01% by weight of an oil soluble reaction product of lauryl acid phosphate and di-2-ethyl hexylamine, and about 0.1% by weight of phenyl alpha naphthylamine.

Description

= s be a corporation of P No l poe Phiiadeip, ennsylvc i i.
r Application August 30, 19%, v
l do designer I to Serial No. 551,997
The present invention relates to lubricant compositions, and more particularly to rust-inhibiting lubricants suitable for the lubrication of steam turbines, internal combustion engines, gears, cables, and other metal surfaces exposed to rusting or corroding conditions during use.
The lubricant of the present invention is especially adapted for use in the lubrication of steam turbines, and has proved very satisfactory in inhibiting rust and corrosion of turbine parts, such rusting normally being caused by the steam condensate entrained in the lubricants heretofore employed.
The lubricant of the present invention is not only satisfactory from the view point of rustinhibition, but is likewise substantially unafiected by steam or water and retains a gooddemulsibility value during its use in steam turbines.
'In accordanc with the present invention, there is added to a hydrocarbon oil, such as lubricating oil of suitable viscosity, a small quantity of an oil-soluble reaction product of an alkyl acid phosphat having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing from d to 16 carbon atoms in the alkyl group. Such reaction product is preferably pnepared by bringing equimolar quantities of thereactants to a temperature between 100 F. and 200 F. and efiecting reaction between the components at such temperature. It is believed, although not definitely known, that the reaction produces an addition salt since no byproducts appear to b formed. The reaction. is usually fairly rapid, with the evolution of heat, and the reaction product usually comprises a clear, reddish-brown, viscous oil. It is not necessary in all cases to use exactly euuimolar proportions of the acid phosphate and the amine, since it has been found desirable to have the reaction product slightly on the alkaline side, with a pH of about 8. This is accomplished by employing a slight excess of the amine over that required for complete neutralization of the acid phosphate. While it is preferred to cause direct reaction between the amine and the acid phosphate, such reaction may be carried out by adding the reactants to hydrocarbon oil, and then adjusting the. temperature of the mixture to effect reaction,
' thus producing a hydrocarbon oil solution or the reaction product, which. if desired, may "be further diluted with additional oil.
The alkyl acid phosphates which may be utilined in making up the reaction product are the monoor dialwl acid phosphates having from 8 to 16 carbon atoms in the alkyl group. a
monoand diesters, or ixtures thereohmay be I exemplified by the monoand diphosphoridacld esters of octyl alcohol, .nonyl alcohol, tetradecyl alcohol,
simple monoor diesters or mixtures of monoand diesters, and the alcohols employed in the manufacture of the esters may besingle alcohols or mixtures of such-alcohols of from 8 to lfi-carbon atoms, the alcohols having either s. straightchain or a branched-chain structure.
The branched-chain alkylamines containing from 4 to 1!) carbon atomsjwhich may be used in the production-of the reaction product includeprimary, secondary, and tertiary amines, or mixtures of two or more thereof.- Exemplary of these compounds, all of which are characterized by the presence of branched-chain alkyl groups,
are mono-, di-, and tri-isobutyl amines, tertiary butyl amines, iso-amylamlnes, secondary amylamines, tertiary amylamines, the branched-chain hexylamines, heptylamlnes. octylamines, nonylamines, decylamines, undecylamines, dodecylamines, tridecylamines, tetradecylandnes, pentadecylamines, and hexadecylamines. In general. any alkylamine having a carbon chain of 4; to 10 carbon atoms and at least-one substituent alkyl group of 1 to 4 carbons, constituting in into a branched-chain alkylamine, may be employed.
In preparing the improved lubricant containing the rust-inhibiting reaction product, there also may be added a small quantity of an antioxidant suitable for inhibiting the development of acidity or of sludge in the oil. Various amines or phenolic compounds may be employed. preferably a naphthylamine such as phenyl alpha naphthylamine, although other amines compatible with the rust inhibitor may be used.
The quantity of'rust inhibiting reaction product to be added to the lubricant is usually small and falls within the range of 0.005% to 1%, the we ferred amount being from 0.01% to 0.1% by weight. The antioxidant which may be utilized 0 in conjunction with the rust inhibitor has been found satisfactory in amounts ranging ,from
0.05% to 0.5 by weight. 0.1% to 0.2% bein preferred.
The present invention may be further illus- I trated by the following example, which. however. is not to be construed as limiting the scope thereof.
A mixture of monoand dilauryl acid phosalcohol, decyl alcohol, undecyl alcohol, dodecyl alcohol, tridecyl pentadecyl alcohol, i and hexadecyl alcohol. The acid esters may be Blank oil"...
the mixture was added di-Z-ethyl hexylamine, the temperature or the mixture being adjusted to about 130 F. The mixture was thoroughly agitated and during the ensuing reaction, the temperature rose to about 200 F. The quantity of amine added was suflicient to bring the pH of the reaction product to about 8, and in the case of these specific reactants, it was found that 1.1 parts by weight of the lauryl acid phosphate required 1 part by weight of di-2-ethyl hexylamine to produce the desired product of pH8, 'the amine being present in slight excess of that required for complete neutralization. The resulting reaction product, which appeared to be an addition salt, consisted of a clear, reddish-brown, viscous oil. This material was added in various percentages, with and without an antioxidant, i. e., phenyl alphanaphthylamine, to a selective solvent refined lubricating oil having an A. P. I. gravityof 32 and a Saybolt universal viscosity of 155 seconds at 100 F. The blank oil and the blends were then tested for rust inhibiting properties in accordance with the A. S. T. M. Method D 665-42T entitled Method of Test for Rust Preventing Characteristics of Steam Turbine Oils in the Presence of Water. Such test comprised essentially immersing a polished steel strip in a beaker containing 300 cc. of oil to be tested, raising the temperature of the oil to 140 F. and stirring for /2 hour, removing 50 cc. of the oil and replacing with 30 cc. of water, continuing the 4 effective for the designated purpose, does not increase the steam emulsion number or the neutralization number beyond permissible limits.
The lubricants of this invention, while especially adapted to the lubrication of steam turbines, are alsosuitable for use in many other mechanisms including internal combustion engines, compressors, gears, and the like.
. I claim:
l. A lubricant comprising hydrocarbon oil and a rust-inhibiting quantity of an oil-soluble reaction product 01 an alkyl acid phosphate having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing from 4 to 16 carbon atoms in the alkyl group.
2. A lubricant comprising hydrocarbon oil, a rust-inhibiting quantity of an oil-soluble reaction product 01 an alkyl acid phosphate having from 8'-to 16 carbon atoms in the alkyl group and a branched-chain alkylamin'e containing i'rom 4 to 16 carbon atoms in the alkyl group, and air amine antioxidant.
3. A lubricant comprising hydrocarbon oil and i from 0.005% to 1.0% by weight or an oil-soluble stirring at 140 F. for 48 hours, removing the steel strip and washing it with naphtha to remove oil, and examining the strip for the percent surface rusted.
The results of the tests with the various oil compositions are given in the following table.
Condition of steel strip 80 Blank oil+0.25% reaction product 0 0 Blank oi l+0.05% reaction product... Blank o1i+0.0l% reaction product Blank oil+0.0l% reaction product-H) antioxidant 3 GOO QOO
! Luuryl acid phosphate-di-2ethyl hexylamine.
' Phcnyl alpha naphthylamine.
As will be seen from the above data, the reaction product is compatible with the oxidation inhibitor, and its rust inhibiting qualities are not destroyed by the washing action of water. Furthermore the presence of the inhibitor, with or without the antioxidant, in the concentrations reaction product of an alkyl acid phosphate having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing from 4 to 16 carbon atoms in the alkylgroup.
4., A lubricant comprising hydrocarbon .oil, from 0.005% to 1.0% by weight of an oil-soluble reaction product of an alkyl acid phosphate having from 8 to 16 carbon atoms in the alkyl group and a branched-chain alkylamine containing 1mm 4 to 16 carbon atoms in the alkyl group, and from 0.05% to 0.5% by weight of an amine antioxidant.
5. A lubricant comprising hydrocarbon oil and a rust-inhibiting quantity of an oil-soluble reaction product of lauryl acid phosphate and (11-2- ethyl hexylamine.
6. A lubricant comprising hydrocarbon oil, a rust-inhibiting quantity or an oil-soluble reaction product of lauryl acid phosphate and di-2-ethyl hexylamine, and an oxidation-inhibiting quantity of a naphthylamine.
7. A lubricant comprising hydrocarbon oil, from 0.005% to 1.0% by weight of an oil-soluble reaction product oi. lauryl acid,phosphate and di-2-ethyl hexylamine, and irom 0.05% to 0.5% by weight of phenyl alpha naphthylamine.
8. A lubricant comprising hydrocarbon oil, about 0.01% by weight of an oil soluble reaction product of lauryl acid phosphate and di-2-ethyl hexylamine, and about 0.1% by weight of phenyl alpha naphthylamine.
US551997A 1944-08-30 1944-08-30 Rust-inhibiting lubricant Expired - Lifetime US2413852A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US551997A US2413852A (en) 1944-08-30 1944-08-30 Rust-inhibiting lubricant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US551997A US2413852A (en) 1944-08-30 1944-08-30 Rust-inhibiting lubricant

Publications (1)

Publication Number Publication Date
US2413852A true US2413852A (en) 1947-01-07

Family

ID=24203523

Family Applications (1)

Application Number Title Priority Date Filing Date
US551997A Expired - Lifetime US2413852A (en) 1944-08-30 1944-08-30 Rust-inhibiting lubricant

Country Status (1)

Country Link
US (1) US2413852A (en)

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2515520A (en) * 1949-08-16 1950-07-18 Tide Water Associated Oil Comp Rust-inhibiting lubricating oil
US2516914A (en) * 1947-03-21 1950-08-01 Tide Water Associated Oil Comp Emulsification-inhibited polyacrylate-containing oil compositions
US2574954A (en) * 1947-09-23 1951-11-13 Tide Water Associated Oil Comp Rust-inhibiting compositions
US2574955A (en) * 1948-07-14 1951-11-13 Tide Water Associated Oil Comp Esterified alkylolamine salts of acid esters of phosphorus acids
US2605226A (en) * 1949-11-30 1952-07-29 Tide Water Associated Oil Comp Compounded lubricating oil
US2656375A (en) * 1951-09-06 1953-10-20 Tide Water Associated Oil Comp Amino bicyclohexyl-alkyl acid phosphate reaction product
US2664400A (en) * 1949-08-13 1953-12-29 Victor Chemical Works Reaction products of an octyl acid pyrophosphate and soyamine and lubricants containing the same
US2728643A (en) * 1951-12-03 1955-12-27 Tide Water Associated Oil Comp Corrosion inhibited gasoline
US2728728A (en) * 1951-09-28 1955-12-27 Tide Water Associated Oil Comp Anti-corrosion turbine oil
US2728645A (en) * 1952-04-01 1955-12-27 Tide Water Associated Oil Comp Anticorrosive gasoline
US2758086A (en) * 1952-06-28 1956-08-07 California Research Corp Lubricant composition
US2776955A (en) * 1953-07-09 1957-01-08 Hercules Powder Co Ltd Reaction product of stabilized rosin amine with phosphorus pentoxide
US2824068A (en) * 1953-11-17 1958-02-18 Exxon Research Engineering Co Additive-containing oil compositions and the like
US2891909A (en) * 1955-11-16 1959-06-23 Cities Service Res & Dev Co Method of inhibiting corrosion of metals
US2948685A (en) * 1954-06-04 1960-08-09 Gulf Oil Corp Bore cleaning compositions
US3080222A (en) * 1960-02-23 1963-03-05 Gulf Research Development Co Oxo-octyl amine salts of dioxo-octyl phosphoric acid esters
US3088910A (en) * 1959-08-10 1963-05-07 Exxon Research Engineering Co Corrosion inhibitors
US3108070A (en) * 1960-08-08 1963-10-22 Atlantic Refining Co Lubricating oil compositions and fireresistant lubricating emulsions produced therefrm
US3146208A (en) * 1960-12-29 1964-08-25 Monsanto Co Corrosion inhibition
US3228758A (en) * 1961-10-24 1966-01-11 Du Pont Fuels containing amine salts of alkyl acid phosphates
US3397150A (en) * 1966-03-15 1968-08-13 Du Pont Composition and method for treating surfaces
US3516922A (en) * 1966-03-09 1970-06-23 Du Pont Method of inhibiting corrosion
US4146490A (en) * 1977-12-02 1979-03-27 Fmc Corporation Turbine lubricant
US4169800A (en) * 1977-12-02 1979-10-02 Fmc Corporation Turbine lubricant
US4171272A (en) * 1977-12-02 1979-10-16 Fmc Corporation Turbine lubricant
US4755311A (en) * 1986-08-14 1988-07-05 The Lubrizol Corporation Phosphorus-, sulfur- and boron-containing compositions, and lubricant and functional fluid compositions containing same
US5354484A (en) * 1986-06-13 1994-10-11 The Lubrizol Corporation Phosphorus-containing lubricant and functional fluid compositions

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2516914A (en) * 1947-03-21 1950-08-01 Tide Water Associated Oil Comp Emulsification-inhibited polyacrylate-containing oil compositions
US2574954A (en) * 1947-09-23 1951-11-13 Tide Water Associated Oil Comp Rust-inhibiting compositions
US2574955A (en) * 1948-07-14 1951-11-13 Tide Water Associated Oil Comp Esterified alkylolamine salts of acid esters of phosphorus acids
US2664400A (en) * 1949-08-13 1953-12-29 Victor Chemical Works Reaction products of an octyl acid pyrophosphate and soyamine and lubricants containing the same
US2515520A (en) * 1949-08-16 1950-07-18 Tide Water Associated Oil Comp Rust-inhibiting lubricating oil
US2605226A (en) * 1949-11-30 1952-07-29 Tide Water Associated Oil Comp Compounded lubricating oil
US2656375A (en) * 1951-09-06 1953-10-20 Tide Water Associated Oil Comp Amino bicyclohexyl-alkyl acid phosphate reaction product
US2728728A (en) * 1951-09-28 1955-12-27 Tide Water Associated Oil Comp Anti-corrosion turbine oil
US2728643A (en) * 1951-12-03 1955-12-27 Tide Water Associated Oil Comp Corrosion inhibited gasoline
US2728645A (en) * 1952-04-01 1955-12-27 Tide Water Associated Oil Comp Anticorrosive gasoline
US2758086A (en) * 1952-06-28 1956-08-07 California Research Corp Lubricant composition
US2776955A (en) * 1953-07-09 1957-01-08 Hercules Powder Co Ltd Reaction product of stabilized rosin amine with phosphorus pentoxide
US2824068A (en) * 1953-11-17 1958-02-18 Exxon Research Engineering Co Additive-containing oil compositions and the like
US2948685A (en) * 1954-06-04 1960-08-09 Gulf Oil Corp Bore cleaning compositions
US2891909A (en) * 1955-11-16 1959-06-23 Cities Service Res & Dev Co Method of inhibiting corrosion of metals
US3088910A (en) * 1959-08-10 1963-05-07 Exxon Research Engineering Co Corrosion inhibitors
US3080222A (en) * 1960-02-23 1963-03-05 Gulf Research Development Co Oxo-octyl amine salts of dioxo-octyl phosphoric acid esters
US3108070A (en) * 1960-08-08 1963-10-22 Atlantic Refining Co Lubricating oil compositions and fireresistant lubricating emulsions produced therefrm
US3146208A (en) * 1960-12-29 1964-08-25 Monsanto Co Corrosion inhibition
US3228758A (en) * 1961-10-24 1966-01-11 Du Pont Fuels containing amine salts of alkyl acid phosphates
US3516922A (en) * 1966-03-09 1970-06-23 Du Pont Method of inhibiting corrosion
US3397150A (en) * 1966-03-15 1968-08-13 Du Pont Composition and method for treating surfaces
US4146490A (en) * 1977-12-02 1979-03-27 Fmc Corporation Turbine lubricant
US4169800A (en) * 1977-12-02 1979-10-02 Fmc Corporation Turbine lubricant
US4171272A (en) * 1977-12-02 1979-10-16 Fmc Corporation Turbine lubricant
US5354484A (en) * 1986-06-13 1994-10-11 The Lubrizol Corporation Phosphorus-containing lubricant and functional fluid compositions
US4755311A (en) * 1986-08-14 1988-07-05 The Lubrizol Corporation Phosphorus-, sulfur- and boron-containing compositions, and lubricant and functional fluid compositions containing same

Similar Documents

Publication Publication Date Title
US2413852A (en) Rust-inhibiting lubricant
US2736706A (en) Lubricant containing a phosphorus acid ester-aldehyde condensation product
US2174019A (en) Lubricant
US2245649A (en) Lubricant and method of making same
US3169923A (en) Oil of lubricating viscosity
US3203895A (en) Lubricating oils containing amine salts of phosphates
US2587546A (en) Rust inhibiting composition
US2503401A (en) Lubricants
US2353558A (en) Addition agent for lubricating oil and method of making same
US2779739A (en) Turbine lubricating oil compositions
US2261888A (en) Steam turbine lubrication
US2415353A (en) Rust preventing turbine oil
US2485150A (en) Mineral oil compositions
US2605226A (en) Compounded lubricating oil
US2209464A (en) Lubricant
US2709156A (en) Oxidation-inhibited mineral oil compositions
US2344886A (en) Lubricant composition
US2485341A (en) Rust inhibiting composition
US2326140A (en) Lubricant
US2362332A (en) Corrosion preventive compositions
US2442581A (en) Rust-preventive composition
US2634237A (en) Rust inhibiting composition
US2450321A (en) Rust-inhibiting greases
US2718500A (en) Rust inhibited composition
US2989464A (en) Stabilized suspensions of calcium acetate in oil