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WO2005071048A1 - Extreme pressure lubricant additive and method of making same - Google Patents

Extreme pressure lubricant additive and method of making same Download PDF

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Publication number
WO2005071048A1
WO2005071048A1 PCT/CA2005/000088 CA2005000088W WO2005071048A1 WO 2005071048 A1 WO2005071048 A1 WO 2005071048A1 CA 2005000088 W CA2005000088 W CA 2005000088W WO 2005071048 A1 WO2005071048 A1 WO 2005071048A1
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WO
WIPO (PCT)
Prior art keywords
extreme pressure
lubricants
pressure additive
phosphate ester
butylated hydroxytoluene
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.)
Ceased
Application number
PCT/CA2005/000088
Other languages
French (fr)
Inventor
Christopher Malyszewicz
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.)
ENN ENVIRONMENTAL NUTRITION NETWORK CORP
Original Assignee
ENN ENVIRONMENTAL NUTRITION NETWORK CORP
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ENN ENVIRONMENTAL NUTRITION NETWORK CORP filed Critical ENN ENVIRONMENTAL NUTRITION NETWORK CORP
Publication of WO2005071048A1 publication Critical patent/WO2005071048A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • C10M157/00Lubricating compositions characterised by the additive being a mixture of two or more macromolecular compounds covered by more than one of the main groups C10M143/00 - C10M155/00, each of these compounds being essential
    • C10M157/08Lubricating compositions characterised by the additive being a mixture of two or more macromolecular compounds covered by more than one of the main groups C10M143/00 - C10M155/00, each of these compounds being essential at least one of them being a 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
    • C10M137/00Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
    • C10M137/02Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
    • C10M137/04Phosphate esters
    • 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
    • C10M169/00Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04Mixtures of base-materials and 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/06Well-defined aromatic compounds
    • 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
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/104Aromatic fractions
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • C10M2215/042Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • 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
    • 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
    • C10N2020/00Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
    • C10N2020/01Physico-chemical properties
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/06Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
    • 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
    • C10N2040/25Internal-combustion engines

Definitions

  • the invention relates to the field of lubricant additives, and more particularly relates to the field of extreme pressure additives suitable for addition to engine oils and other lubricants.
  • Chlorine-based compounds such as the chlorine derivates of paraffinic hydrocarbon compounds referred to as chlorinated paraffins
  • chlorinated paraffins have long been used as lubricant additives to improve the performance of the lubricant under extreme pres- sure.
  • the liquid lubricant is forced from the area of contact between the two metal surfaces, but when an extreme pressure additive such as chlorinated paraffin is present, the heat generated between the two surfaces causes chlorine atoms to be liberated from the additive and to combine with the surface metal.
  • This causes a surface coating of a chloride, such as iron chloride, to be formed.
  • This surface coating of chloride has a much lower coefficient of fiiction than the dry metal surface and fills in depressions in the surfaces, resulting in smoother surfaces at the point of contact and reduced friction and wear.
  • chlorinated paraffins have various problems, including serious environmental problems such that products containing them are deemed unsuitable for safe disposal in the environment.
  • the corrosive nature of chlorinated paraffins have made them generally unsuitable for use in internal combustion engine applications or other corrosion-sensitive applications. Under heating, the chlorinated paraffins release hydrochloric gas then subsequently hydrochloric acid, which is corrosive. They also are an initant and harmful when in contact with skin.
  • Chlorinated paraffins are thermally unstable and above 200°C degrade, generating strong acid radicals in the form of hydrogen chloride and free chloride ions. These radicals attack metal surfaces to form chloride films of the metal, which may lead to stress crack corrosion which causes detriment to the structural materials, corrosion of bearings, piston and valve trains and eventual mechanical failure.
  • Phosphate esters have been known as a component of motor oils compositions. See for example United States Patent no. 3,547,820 Woodward et al. A problem with such formulations is avoiding hydrolysis of the base material as it encounters sustained high temperatures.
  • an extreme pressure lubricant additive comprising between 50% and 70% and preferably about 65.915 % of a motor oil; between 12% and 20% and preferably about 16 % of a phosphate ester such as Crodaphos CO5A; between 5% and 20% and preferably about 12.5 % of an aromatic antistatic solvent such as Solvesso 100; between .2% and 1.5% and preferably about 0.897 % Calcium Sulphonate; between .01% and .9% and preferably about .688 % of a butylated hydroxytoluene such as Topanol O; and between 0% and 6% and preferably about 4% Triethanolamine.
  • an extreme pressure lubricant additive consisting essentially of: (a) approximately 65.9 volume percent motor oil; (b) approximately 16 volume percent phosphate ester; (c) approxi- mately 12.5 volume percent of an aromatic solvent; (d) approximately .9 volume percent of an alkaline earth metal sulphonate; (e) approximately .7 volume percent of an anti-oxidant such as butylated hydroxytoluene; and (f) approximately 4 volume percent of Triethanolamine.
  • a method of producing an extreme pressure additive for lubricants comprising the steps of: a) pre-heating the phosphate ester (e.g.
  • Crodophos C05A to 34 degrees C; b) pre- ixing Solvesso and Topanol until dissolved and premix with Crodaphos CO5A; c) add calcium sulphonate to b); d) adding triethanolamine 100% preheated to 35 degrees C to base oil and stirring; e) stir for at least 20 minutes then add the premixed SOLVESSO and TOPANOL f) Stir for 30 minutes to give a clear pale yellow viscous liquid.
  • Phosphate esters in general are non-classified and are considered safe to handle compounds. They do not possess the unpleasant characteristics of the chlorinated paraffins. Initially when the phosphate esters were first developed, hydrolysis was a constant problem and thermal stability was another. This has been overcome by the use of combinations of oelyl and cetyl alcohol derivatives which are esterified to form acid esters. These require neutralising utilising a safe but suitable element or compound. The molecule of water generated by condensation is incorporated by the ethoxylated ester and is released slowly over time.
  • phosphate esters are their thermal stability, slow degradation and where there is any formation of a phosphate acid radical, metal surfaces are coated on a mono-molecular basis to self inhibit further chemical interaction.
  • the coating lends itself to increased absorption of extreme pressure additive thus further enhancing the performance of the phosphate ester.
  • phosphate esters is non-corrosive towards metal surfaces as an extreme pressure additive and is more environmentally friendly than chlor paraffins.
  • the phosphate ester systems are environmentally approved due to their safety and non- bioaccumulation. Disposal of products containing this type of extreme pressure additive is safe and no regulatory information is required for disposal.
  • the preferred form of additive according to the invention has the following composition (percentages are shown by volume):
  • base motor oil such as Castrol E20 motor oil 16 % Crodaphos CO5A 12.5 % anti-static solvent such as Solvesso 100 0.897 % Calcium Sulphonate 0.688 % anti-oxidant such as butylated hydroxytoluene; Topanol O 4% Triethanolamine.
  • composition will also work within the following approximate ranges: between 50% and 70% and preferably about 65.915 % of a motor oil; between 12% and 20% and preferably about 16 % of a phosphate ester such as Crodaphos CO5A; between 5% and 20% and preferably about 12.5 % of an aromatic antistatic solvent such as Solvesso 100; between .2% and 1.5% and preferably about 0.897 % Calcium Sulphonate; between .01% and .9% and preferably about .688 % of a butylated hydiOxytoluene such as Topanol O; and between 0% and 6% and preferably about 4% Triethanolamine.
  • a phosphate ester such as Crodaphos CO5A
  • aromatic antistatic solvent such as Solvesso 100
  • Solvesso 100 between .2% and 1.5% and preferably about 0.897 % Calcium Sulphonate
  • the following method is used to produce the extreme pressure additive.
  • First the base motor oil is added to the mixing container.
  • the Crodaphos C05A is preheated to 34 degrees Centigrade.
  • the Solvesso and Topanol are then pre-mixed until dissolved and are then premixed with the Crodaphos CO5A.
  • the calcium sulphonate is added to the pre-mixed Solvesso, Topanol and Crodaphos.
  • the Triethanolamine 100% is preheated to 35 degrees C and added to the base oil and mixed, such as by stirring for at least 20 minutes, and the pre-mixed calcium sulphonate, Solvesso, Topanol and Crodaphos is then added.
  • the final mixture is then mixed such as by stirring for 30 minutes to give a clear pale yellow viscous liquid.
  • the result of this final blending process is the extreme pressure additive of the invention.
  • the final product is used by adding it to the motor engine oil preferably in a 5% to 10% proportion.
  • the lubricant additive of the invention may also be added to other lubricants and fluids such as greases (where a proportion of approximately 4% to 12% by volume of the additive is preferred), metal cutting lubricants, industrial gear lubricants, hydraulic oils (excluding hydraulic brake fluid), automatic transmission fluid, power steering fluid, penetrating oil, air conditioner refrigerant, and as a coating for brass.
  • the additive of the invention serves to reduce friction and metal wear under extreme pressure situations, and also serves to reduce corrosion. It has also been found that by adding the extreme pressure additive product of the invention to a gasoline or diesel fuel conditioner, the performance of the internal combustion engine may be improved through lubrication of the moving metal parts which come into contact with the fuel in the upper end of the engine.
  • the acid radical developed will be the acid phosphate ion which produces a tenacious phosphate film on ferrous surfaces which, in turn, generates a protective film. This attracts more extreme pressure additive onto the surface, acting as a sponge to absorb the base materials.
  • the phosphate system does not cause damage and thereby, when the phosphate film is formed, creates a protective coating on the metal surface thereby inhibiting any further attack.
  • Crodaphos CO5A has been specified as the appropriate phosphate ester, other phosphate esters having similar properties would also be suitable for use in the invention.
  • calcium sulfonate has been specified as the appropriate sulfonate other alkaline earth metal sulfonates having similar properties, such as barium sulfonate, would also be suitable for use in the invention.
  • Solvesso 100 has been specified as the appropriate anti-static solvent, other solvents having similar properties, would also be suitable for use in the invention.

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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)

Abstract

An extreme pressure. additive and a method of making same are provided. The additive comprises between 50% and 70% of a motor oil; between 10% and 20% of a phosphate ester; between 5% and 20% of an aromatic antistatic; between .2% and 1.5% Calcium Sulphonate; between .01% and. .9% of a butylated hydroxytoluene; and between 0% and 6% Triethanolamine.

Description

EXTREME PRESSURE LUBRICANT ADDITIVE AND METHOD OF MAKING SAME
Reference to Related Application
This application claims the benefit of United States Provisional application no. 60/539,222 filed January 26, 2004.
Technical Field
The invention relates to the field of lubricant additives, and more particularly relates to the field of extreme pressure additives suitable for addition to engine oils and other lubricants.
Background
Chlorine-based compounds, such as the chlorine derivates of paraffinic hydrocarbon compounds referred to as chlorinated paraffins, have long been used as lubricant additives to improve the performance of the lubricant under extreme pres- sure. In extreme pressure conditions, the liquid lubricant is forced from the area of contact between the two metal surfaces, but when an extreme pressure additive such as chlorinated paraffin is present, the heat generated between the two surfaces causes chlorine atoms to be liberated from the additive and to combine with the surface metal. This causes a surface coating of a chloride, such as iron chloride, to be formed. This surface coating of chloride has a much lower coefficient of fiiction than the dry metal surface and fills in depressions in the surfaces, resulting in smoother surfaces at the point of contact and reduced friction and wear.
The use of chlorinated paraffins has various problems, including serious environmental problems such that products containing them are deemed unsuitable for safe disposal in the environment. The corrosive nature of chlorinated paraffins have made them generally unsuitable for use in internal combustion engine applications or other corrosion-sensitive applications. Under heating, the chlorinated paraffins release hydrochloric gas then subsequently hydrochloric acid, which is corrosive. They also are an initant and harmful when in contact with skin. Chlorinated paraffins are thermally unstable and above 200°C degrade, generating strong acid radicals in the form of hydrogen chloride and free chloride ions. These radicals attack metal surfaces to form chloride films of the metal, which may lead to stress crack corrosion which causes detriment to the structural materials, corrosion of bearings, piston and valve trains and eventual mechanical failure.
Phosphate esters have been known as a component of motor oils compositions. See for example United States Patent no. 3,547,820 Woodward et al. A problem with such formulations is avoiding hydrolysis of the base material as it encounters sustained high temperatures.
Surnrnary of Invention
The present invention provides an extreme pressure additive suitable for use in internal combustion engine lubricants or other applications where corrosion must be ' avoided. According to one aspect of the invention, there is provided an extreme pressure lubricant additive comprising between 50% and 70% and preferably about 65.915 % of a motor oil; between 12% and 20% and preferably about 16 % of a phosphate ester such as Crodaphos CO5A; between 5% and 20% and preferably about 12.5 % of an aromatic antistatic solvent such as Solvesso 100; between .2% and 1.5% and preferably about 0.897 % Calcium Sulphonate; between .01% and .9% and preferably about .688 % of a butylated hydroxytoluene such as Topanol O; and between 0% and 6% and preferably about 4% Triethanolamine. Thus the invention provides an extreme pressure lubricant additive consisting essentially of: (a) approximately 65.9 volume percent motor oil; (b) approximately 16 volume percent phosphate ester; (c) approxi- mately 12.5 volume percent of an aromatic solvent; (d) approximately .9 volume percent of an alkaline earth metal sulphonate; (e) approximately .7 volume percent of an anti-oxidant such as butylated hydroxytoluene; and (f) approximately 4 volume percent of Triethanolamine. Further according to the invention there is provided a method of producing an extreme pressure additive for lubricants comprising the steps of: a) pre-heating the phosphate ester (e.g. Crodophos C05A) to 34 degrees C; b) pre- ixing Solvesso and Topanol until dissolved and premix with Crodaphos CO5A; c) add calcium sulphonate to b); d) adding triethanolamine 100% preheated to 35 degrees C to base oil and stirring; e) stir for at least 20 minutes then add the premixed SOLVESSO and TOPANOL f) Stir for 30 minutes to give a clear pale yellow viscous liquid.
Description Throughout the following description, specific details are set forth in order to provide a more thorough understanding of the invention. However, the invention may be practiced without these particulars. In other instances, well known elements have not been shown or described in detail to avoid unnecessarily obscuring the invention. Accordingly, the specification and drawings are to be regarded in an illustrative, rather than a restrictive, sense.
Phosphate esters in general are non-classified and are considered safe to handle compounds. They do not possess the unpleasant characteristics of the chlorinated paraffins. Initially when the phosphate esters were first developed, hydrolysis was a constant problem and thermal stability was another. This has been overcome by the use of combinations of oelyl and cetyl alcohol derivatives which are esterified to form acid esters. These require neutralising utilising a safe but suitable element or compound. The molecule of water generated by condensation is incorporated by the ethoxylated ester and is released slowly over time.
The main distinct advantages of the new generation of phosphate esters are their thermal stability, slow degradation and where there is any formation of a phosphate acid radical, metal surfaces are coated on a mono-molecular basis to self inhibit further chemical interaction. The coating lends itself to increased absorption of extreme pressure additive thus further enhancing the performance of the phosphate ester. Thus the use of phosphate esters is non-corrosive towards metal surfaces as an extreme pressure additive and is more environmentally friendly than chlor paraffins.
In the case of chlor paraffins, if engine oil containing this material is not changed on time then severe damage will result to bearings and all moving parts of the engine whereas with a phosphate ester compound this does not occur. The phosphate ester systems are environmentally approved due to their safety and non- bioaccumulation. Disposal of products containing this type of extreme pressure additive is safe and no regulatory information is required for disposal. The preferred form of additive according to the invention has the following composition (percentages are shown by volume):
65.915 % base motor oil, such as Castrol E20 motor oil 16 % Crodaphos CO5A 12.5 % anti-static solvent such as Solvesso 100 0.897 % Calcium Sulphonate 0.688 % anti-oxidant such as butylated hydroxytoluene; Topanol O 4% Triethanolamine. The composition will also work within the following approximate ranges: between 50% and 70% and preferably about 65.915 % of a motor oil; between 12% and 20% and preferably about 16 % of a phosphate ester such as Crodaphos CO5A; between 5% and 20% and preferably about 12.5 % of an aromatic antistatic solvent such as Solvesso 100; between .2% and 1.5% and preferably about 0.897 % Calcium Sulphonate; between .01% and .9% and preferably about .688 % of a butylated hydiOxytoluene such as Topanol O; and between 0% and 6% and preferably about 4% Triethanolamine.
The following method is used to produce the extreme pressure additive. First the base motor oil is added to the mixing container. The Crodaphos C05A is preheated to 34 degrees Centigrade. The Solvesso and Topanol are then pre-mixed until dissolved and are then premixed with the Crodaphos CO5A. The calcium sulphonate is added to the pre-mixed Solvesso, Topanol and Crodaphos. The Triethanolamine 100% is preheated to 35 degrees C and added to the base oil and mixed, such as by stirring for at least 20 minutes, and the pre-mixed calcium sulphonate, Solvesso, Topanol and Crodaphos is then added. The final mixture is then mixed such as by stirring for 30 minutes to give a clear pale yellow viscous liquid. The result of this final blending process is the extreme pressure additive of the invention. The final product is used by adding it to the motor engine oil preferably in a 5% to 10% proportion. In addition to serving as an extreme pressure additive for motor oils, the lubricant additive of the invention may also be added to other lubricants and fluids such as greases (where a proportion of approximately 4% to 12% by volume of the additive is preferred), metal cutting lubricants, industrial gear lubricants, hydraulic oils (excluding hydraulic brake fluid), automatic transmission fluid, power steering fluid, penetrating oil, air conditioner refrigerant, and as a coating for brass. In all these applications, the additive of the invention serves to reduce friction and metal wear under extreme pressure situations, and also serves to reduce corrosion. It has also been found that by adding the extreme pressure additive product of the invention to a gasoline or diesel fuel conditioner, the performance of the internal combustion engine may be improved through lubrication of the moving metal parts which come into contact with the fuel in the upper end of the engine.
The main advantages of the new ester system is that even during hydrolysis, if this should occur, the acid radical developed will be the acid phosphate ion which produces a tenacious phosphate film on ferrous surfaces which, in turn, generates a protective film. This attracts more extreme pressure additive onto the surface, acting as a sponge to absorb the base materials. Unlike chlor paraffins which release acid radicals which are extremely corrosive and damage ferrous and non-ferrous surfaces, the phosphate system does not cause damage and thereby, when the phosphate film is formed, creates a protective coating on the metal surface thereby inhibiting any further attack. If the engine oil is not changed on time it is likely that corrosive elements will be formed but due to the nature of the phosphate ion, no further chemical damage will be done to engine parts. While Crodaphos CO5A has been specified as the appropriate phosphate ester, other phosphate esters having similar properties would also be suitable for use in the invention. While calcium sulfonate has been specified as the appropriate sulfonate other alkaline earth metal sulfonates having similar properties, such as barium sulfonate, would also be suitable for use in the invention. While Solvesso 100 has been specified as the appropriate anti-static solvent, other solvents having similar properties, would also be suitable for use in the invention. While Topanol O has been specified as the appropriate butylated hydroxytoluene, other butylated hydroxytoluenes having similar properties would also be suitable for use in the invention. Thus while a preferred embodiment of the invention has been described, the scope of the invention should not be limited thereto. As will be apparent to those skilled in the art in the light of the foregoing disclosure, many alterations and modifications are possible in the practice of this invention without departing from the spirit or scope thereof. Accordingly, the scope of the invention is to be construed in accordance with the substance defined by the following claims.

Claims

WHAT IS CLAIMED IS:
1. A method of producing an extreme pressure additive for lubricants comprising the steps of: a) pre-heating a phosphate ester to 34 degrees C; b) pre-mixing an antistatic solvent and a butylated hydroxytoluene until dissolved and premixing said mixture with said phosphate ester; c) adding calcium sulphonate to the result of step b); d) adding triethanolamine pre-beated to 35 degrees C to a motor oil and mixing; e) adding the mixture from step c) to the mixture resulting from step d); premixed SOLVESSO and TOPANOL and mixing.
2. The method of claim 1 wherein said phosphate ester is Crodaphos CO5A.
3. The method of claim 1 wherein said aromatic antistatic solvent is Solvesso 100.
4. The method of claim 1 wherein said butylated hydroxytoluene is
Topanol O.
5. The method of claim 1 wherein the mixing step of step d) comprises stirring for at least 20 minutes.
6. The method of claim 1 wherein the mixing step of step e) comprises stirring for at least 30 minutes.
7. An extreme pressure additive for lubricants comprising between 50% and 70% of a motor oil; between 10% and 20% of a phosphate ester; between 5% and
20% of an aromatic antistatic; between .2% and 1.5% Calcium Sulphonate; between .01% and .9% of a butylated hydroxytoluene; and between 0% and 6% Triethanolamine.
8. The extreme pressure additive for lubricants of claim 7 comprising about 65.915 % of amotor oil; about 16 % of a phosphate ester; about 12.5 % of an aromatic antistatic solvent; about 0.897 % Calcium Sulphonate; about .688 % of a butylated hydroxytoluene; and about 4% Triethanolamine.
9. The extreme pressure additive for lubricants of claim 7 wherein said phosphate ester is Crodaphos CO5A.
10. The extreme pressure additive for lubricants of claim 7 wherein said aromatic antistatic solvent is Solvesso 100.
11. The extreme pressure additive for lubricants of claim 7 wherein said butylated hydroxytoluene is Topanol O.
12. The extreme pressure additive for lubricants of claim 8 wherein said phosphate ester is Crodaphos CO5A.
13. The extreme pressure additive for lubricants of claim 8 wherein said aromatic antistatic solvent is Solvesso 100.
14. The extreme pressure additive for lubricants of claim 8 wherein said butylated hydroxytoluene is Topanol O.
15. The extreme pressure additive for lubricants of claim 7 comprising: a) approximately 65.9 volume percent motor oil; b) approximately 16 volume percent phosphate ester; c) approximately 12.5 volume percent of an aromatic solvent; d) approximately .9 volume percent of an alkaline earth metal sulphonate; e) approximately .7 volume percent of an anti-oxidant such as butylated hydroxytoluene; and f) approximately 4 volume percent of Triethanolamine.
PCT/CA2005/000088 2004-01-26 2005-01-26 Extreme pressure lubricant additive and method of making same Ceased WO2005071048A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US53922204P 2004-01-26 2004-01-26
US60/539,222 2004-01-26

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1176076A (en) * 1966-05-27 1970-01-01 Mobil Oil Corp Metal Working Lubricant.
EP0805194A1 (en) * 1995-10-05 1997-11-05 Idemitsu Kosan Company Limited Lubricating oil composition for stepless transmissions and method for lubricating stepless transmissions therewith
CA2397228A1 (en) * 2000-02-08 2001-08-16 Francis Prince Water-soluble aluminium and aluminium alloys hot rolling composition
US20020032129A1 (en) * 1999-08-11 2002-03-14 Samuel H. Tersigni Zinc and phosphorus containing transmission fluids having enhanced performance capabilities
US6620772B2 (en) * 2001-07-13 2003-09-16 Renewable Lubricants, Inc. Biodegradable penetrating lubricant

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1176076A (en) * 1966-05-27 1970-01-01 Mobil Oil Corp Metal Working Lubricant.
EP0805194A1 (en) * 1995-10-05 1997-11-05 Idemitsu Kosan Company Limited Lubricating oil composition for stepless transmissions and method for lubricating stepless transmissions therewith
US20020032129A1 (en) * 1999-08-11 2002-03-14 Samuel H. Tersigni Zinc and phosphorus containing transmission fluids having enhanced performance capabilities
CA2397228A1 (en) * 2000-02-08 2001-08-16 Francis Prince Water-soluble aluminium and aluminium alloys hot rolling composition
US6620772B2 (en) * 2001-07-13 2003-09-16 Renewable Lubricants, Inc. Biodegradable penetrating lubricant

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