US20030109389A1 - Synthetic industrial oils made with "tri-synthetic" base stocks - Google Patents
Synthetic industrial oils made with "tri-synthetic" base stocks Download PDFInfo
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- US20030109389A1 US20030109389A1 US10/292,096 US29209602A US2003109389A1 US 20030109389 A1 US20030109389 A1 US 20030109389A1 US 29209602 A US29209602 A US 29209602A US 2003109389 A1 US2003109389 A1 US 2003109389A1
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- pao
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M169/00—Lubricating 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
- C10M169/04—Mixtures of base-materials and additives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
- C10M111/04—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential at least one of them being a macromolecular organic compound
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/06—Well-defined aromatic compounds
- C10M2203/065—Well-defined aromatic compounds used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/0206—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/285—Esters of aromatic polycarboxylic acids
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/285—Esters of aromatic polycarboxylic acids
- C10M2207/2855—Esters of aromatic polycarboxylic acids used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/02—Viscosity; Viscosity index
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/30—Anti-misting
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/66—Hydrolytic stability
Definitions
- the present invention relates to lubricant base stock blends. More particularly, the present invention is directed toward base stocks having unexpectedly improved resistance to deposit formation, improved solubility for lubricant additives, degradation products and enhanced demulsibility.
- Synthetic lubricant base stocks prepared by oligomerizing one or more alpha olefins are well known commercially available materials that have low pour points and high viscosity indices.
- Lube products employing these poly-alpha-olefins (PAO's) typically are combined with a more polar co-base stock such as alkylated aromatic fluids or polyol esters or certain dispersant additives such as polyalkylene type additives.
- alkylated aromatic base fluids such as alkylated naphthalene
- PAO base fluids provides the fluid blend with improved hydrolytic stability but there remains a need to provide the blend with improved dispersancy.
- polyalkylene type additives in PAO base fluids provides enhanced dispersancy but these additives form stable emulsions with water and degrade the hydrolytic stability of compositions employing them thereby limiting the use of the blend to applications where water ingress is not a problem.
- one object of the present invention is to provide a lubricant product of improved dispersancy along with good demulsibility and hydrolytic stability.
- the present invention is a synergistic combination of synthetic fluids useful as lubricant base stock blend and comprising about 10 wt % or more of a PAO fluid; about 1 wt % or more of an alkylated aromatic fluid and about 1 wt % or more of an aromatic ester.
- the lubricant base stock comprises:
- FIG. 1 is a graphic comparison of the storage stability of a commercial lubricant composition with one using a base stock of the invention.
- FIG. 2 graphically illustrates the deposit control property of a base stock of the invention.
- FIG. 3 graphically compares the water demulsibility of a commercial composition with one using a base stock of the invention.
- FIG. 4 graphically compares the oxidative and hydrolytic stability of two base stocks formulations of the invention with two others.
- a blend of three lubricant fluids viz a PAO, an alkylated aromatic and an aromatic ester has improved solvency for lube additives such as oxidation and rust inhibitors, metal passivators and the like.
- the blend also has improved hydrolytic stability, dispersancy and resistance to deposit formation without degrading demulsibility making the blend useful in a wide range of industrial applications.
- fully formulated lubricant compositions employing the base stock of the present invention are especially suitable for use in applications where there is the potential for water of moisture ingress such as oils used in combined cycle turbines, paper machinery, rod mills and the like.
- the blended base stock of the invention includes at least about 10 wt % of a PAO fluid.
- the blend will comprise from about 10 wt % to about 98 wt % of the PAO fluid, based on the total weight of the blend.
- the blend will comprise from 60 wt % to 95 wt %, and more preferably from 80 wt % to 85 wt %.
- PAO fluids and their preparation are well known in the art.
- Those PAO's suitable in the practice of the present invention may be derived from C 2 to about C 32 alpha olefins with C 8 to about C 16 alpha olefins being preferred.
- the PAO will have a viscosity in the range of about 3 cSt to about 300 cSt at 100° C.
- the preferred PAO a viscosity will, of course, depend upon factors such as the nature and amount of the other components used in the blend and the intended end use for the lubricant base stock blend.
- the base stock blend of the present invention also includes a alkylated aromatic compound such as alkylated benzene, naphthalene, anthracene, biphenyl and the like.
- alkylated aromatics and their method of preparation are well known in the art.
- Suitable alkylated aromatics are those having one or more short chain alkyl groups of from 1 to about 8 carbon atoms.
- the preferred alkyl aromatics will have viscosities in the range of about 3 cSt to about 300 cSt at 100° C.
- the alkylated aromatics will comprise about 1 to about 59 wt % of the total blend, preferably about 5 wt % to about 35 wt % and more preferably about 10 wt %.
- the base stock of the present invention also includes an aromatic ester fluid.
- aromatic esters such as phthalate esters, mono- and diesters, polyol ester and ester with tails contain S, N and O suitable in the blend of this invention are commercial available materials typically formed by reacting an organic acid or anhydride with straight or branched alcohols. Such esters have viscosities in the range of about 4 cSt to about 30 cSt at 100° C.
- the amount of aromatic ester employed in the base stock blend will be about 1 wt % to about 75 wt %, and preferably from about 2 wt % to about 25 wt % of the total blend, with about 5 wt % to 8 wt % being more preferred.
- An advantageous feature of the base stock blend of the present invention is its ability to solubilize additives such as heterocyclic rust inhibitors, antioxidants, antiwear agents, corrosion inhibitors and the like.
- additives such as heterocyclic rust inhibitors, antioxidants, antiwear agents, corrosion inhibitors and the like.
- antioxidants suitable for use in the base stock blend specific mention is made of aminic and phenolic type antioxidants.
- Suitable antiwear agents include alkylated triphenyl phosphates, phosphorophites, diorganodithiocarbamates and the like.
- a base stock according to the present invention comprising 84 wt % of a PAO (6 cSt at 100° C.) 10 wt % of an alkyl aromatic (alkylated naphthalene) fluid (5 cSt at 100° C.) and 6 wt % of an ester fluid (diisooctylphthalate) was used in preparing a fully formulated lubricant composition (Formulation A) by blending the base stock with the following additives:
- composition was maintained at 100° C. for 16 weeks without any evidence of haze or floc. Haze or floc, of course, is indicative of additive insolubility.
- FIG. 1 graphically presents the results of the tests and illustrates the improved solubility that the base stock of the invention has for lubricant additives.
- the deposit control of the base stock of the invention was compared to a commercially available lubricant composition (Comparative 2) by subjecting Formulation A of Example 1 and Comparative 2 to the Cincinnati Machine Thermal Test A.
- the Comparative 2 composition has a PAO base fluid, typical additives and 1.0 wt % of a dispersant.
- the results of the text are graphically shown in FIG. 2. As can be seen under the text conditions Formulation A exhibited excellent low deposit formation. Moreover, when the test was modified by raising the test temperature from 275° F. to 350° F. at the end of 168 hours visual inspection of the samples showed that the Formulation A had far less deposit formation.
- Example 3 Formulation A of Example 1 and a commercial lubricant composition (Comparative 3) were subjected to the ASTM-D 1401 demulsibility test. Comparative 3 was a PAO based lubricant containing 1.0 wt % of a polyalkylene dispersant. The results of the tests are shown in FIG. 3.
- Formulation A with the base stock of the invention showed complete water separation within 10 minutes.
- Formulation A did not contain a demulsfier additive.
- This example compares the oxidative and hydroytic stability, as determined by ASTM D 943 TOST life test, of two base stocks of the invention (A and B) with two other base stock (C and D).
- Base stock A comprised 80 wt % PAO (6 cSt at 100° C.); 10 wt % of an alkylated naphthalene (5 cSt at 100° C.) and 6 wt % an ester fluid (diisooctylphthalate).
- Base stock B differed from A in that the ester was a 50:50 mixture of ditridicyl phthalate and terephtalate ester.
- Base stock C and D used the same PAO as A and B.
- the alkylated aromatic fluid of C was the same as in A and B while the ester of D was a trimellitatte ester.
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- Organic Chemistry (AREA)
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Abstract
This invention describes a blend of three base stock fluids, a PAO, an alkylated aromatic and a aromatic ester that synergistically improve the solvency for industrial lubricant additives such as oxidation and rust inhibitors, extreme-pressure/antiwear agents, metal deactivators and the like. The blend also has excellent hydrolytic stability plus improved dispersancy and resistance to deposit formation without degrading demulsibility.
Description
- The present invention relates to lubricant base stock blends. More particularly, the present invention is directed toward base stocks having unexpectedly improved resistance to deposit formation, improved solubility for lubricant additives, degradation products and enhanced demulsibility.
- Synthetic lubricant base stocks prepared by oligomerizing one or more alpha olefins are well known commercially available materials that have low pour points and high viscosity indices. Lube products employing these poly-alpha-olefins (PAO's) typically are combined with a more polar co-base stock such as alkylated aromatic fluids or polyol esters or certain dispersant additives such as polyalkylene type additives.
- The inclusion of alkylated aromatic base fluids such as alkylated naphthalene in PAO base fluids provides the fluid blend with improved hydrolytic stability but there remains a need to provide the blend with improved dispersancy.
- The inclusion of polyalkylene type additives in PAO base fluids provides enhanced dispersancy but these additives form stable emulsions with water and degrade the hydrolytic stability of compositions employing them thereby limiting the use of the blend to applications where water ingress is not a problem.
- The inclusion of polyol esters in PAO base fluids provides good dispersancy but poor hydrolytic stability.
- Therefore, one object of the present invention is to provide a lubricant product of improved dispersancy along with good demulsibility and hydrolytic stability.
- Briefly stated the present invention is a synergistic combination of synthetic fluids useful as lubricant base stock blend and comprising about 10 wt % or more of a PAO fluid; about 1 wt % or more of an alkylated aromatic fluid and about 1 wt % or more of an aromatic ester.
- In a preferred embodiment the lubricant base stock comprises:
- from about 10 wt % to about 98 wt % of a PAO fluid;
- from about 1 wt % to about 59 wt % of an alkylated aromatic; and
- from about 1 wt % to about 75 wt % of an aromatic ester,
- all amounts based on the weight of the blend.
- Advantageous features of the invention will become apparent from the detailed description that follows.
- FIG. 1 is a graphic comparison of the storage stability of a commercial lubricant composition with one using a base stock of the invention.
- FIG. 2 graphically illustrates the deposit control property of a base stock of the invention.
- FIG. 3 graphically compares the water demulsibility of a commercial composition with one using a base stock of the invention.
- FIG. 4 graphically compares the oxidative and hydrolytic stability of two base stocks formulations of the invention with two others.
- Applicant has discovered that a blend of three lubricant fluids, viz a PAO, an alkylated aromatic and an aromatic ester has improved solvency for lube additives such as oxidation and rust inhibitors, metal passivators and the like. The blend also has improved hydrolytic stability, dispersancy and resistance to deposit formation without degrading demulsibility making the blend useful in a wide range of industrial applications. Indeed, fully formulated lubricant compositions employing the base stock of the present invention are especially suitable for use in applications where there is the potential for water of moisture ingress such as oils used in combined cycle turbines, paper machinery, rod mills and the like.
- The blended base stock of the invention includes at least about 10 wt % of a PAO fluid. In general, the blend will comprise from about 10 wt % to about 98 wt % of the PAO fluid, based on the total weight of the blend. Preferably, the blend will comprise from 60 wt % to 95 wt %, and more preferably from 80 wt % to 85 wt %.
- PAO fluids and their preparation are well known in the art. Those PAO's suitable in the practice of the present invention may be derived from C 2 to about C32 alpha olefins with C8 to about C16 alpha olefins being preferred. Typically the PAO will have a viscosity in the range of about 3 cSt to about 300 cSt at 100° C. The preferred PAO a viscosity will, of course, depend upon factors such as the nature and amount of the other components used in the blend and the intended end use for the lubricant base stock blend.
- The base stock blend of the present invention also includes a alkylated aromatic compound such as alkylated benzene, naphthalene, anthracene, biphenyl and the like. Like the PAO's, alkylated aromatics and their method of preparation are well known in the art. Suitable alkylated aromatics are those having one or more short chain alkyl groups of from 1 to about 8 carbon atoms. The preferred alkyl aromatics will have viscosities in the range of about 3 cSt to about 300 cSt at 100° C. The alkylated aromatics will comprise about 1 to about 59 wt % of the total blend, preferably about 5 wt % to about 35 wt % and more preferably about 10 wt %.
- The base stock of the present invention also includes an aromatic ester fluid. Common lubricant grade aromatic esters such as phthalate esters, mono- and diesters, polyol ester and ester with tails contain S, N and O suitable in the blend of this invention are commercial available materials typically formed by reacting an organic acid or anhydride with straight or branched alcohols. Such esters have viscosities in the range of about 4 cSt to about 30 cSt at 100° C. In general, the amount of aromatic ester employed in the base stock blend will be about 1 wt % to about 75 wt %, and preferably from about 2 wt % to about 25 wt % of the total blend, with about 5 wt % to 8 wt % being more preferred.
- An advantageous feature of the base stock blend of the present invention is its ability to solubilize additives such as heterocyclic rust inhibitors, antioxidants, antiwear agents, corrosion inhibitors and the like. Among the antioxidants suitable for use in the base stock blend specific mention is made of aminic and phenolic type antioxidants. Suitable antiwear agents include alkylated triphenyl phosphates, phosphorophites, diorganodithiocarbamates and the like.
- The following examples and comparative examples further illustrate the many advantageous of the instant invention.
- A base stock according to the present invention comprising 84 wt % of a PAO (6 cSt at 100° C.) 10 wt % of an alkyl aromatic (alkylated naphthalene) fluid (5 cSt at 100° C.) and 6 wt % of an ester fluid (diisooctylphthalate) was used in preparing a fully formulated lubricant composition (Formulation A) by blending the base stock with the following additives:
- (1) 0.4 wt % hindered phenolic and diphenyl amine type antioxidants and 1:1 ratio;
- (2) 1.5 wt % butylated triphenyl phosphate type antiwear agent; and
- (3) 0.1 wt % of an ashless rust inhibitor.
- The composition was maintained at 100° C. for 16 weeks without any evidence of haze or floc. Haze or floc, of course, is indicative of additive insolubility.
- In contrast, a commercially available composition comprising a 6 cSt at 100° C. PAO, 20 wt % diisodecylphthalate ester and substantially the same amounts of similar type additives of Formulation A after six weeks displayed a trace of haze and moderate floccing.
- FIG. 1 graphically presents the results of the tests and illustrates the improved solubility that the base stock of the invention has for lubricant additives.
- The deposit control of the base stock of the invention was compared to a commercially available lubricant composition (Comparative 2) by subjecting Formulation A of Example 1 and Comparative 2 to the Cincinnati Machine Thermal Test A. The Comparative 2 composition has a PAO base fluid, typical additives and 1.0 wt % of a dispersant. The results of the text are graphically shown in FIG. 2. As can be seen under the text conditions Formulation A exhibited excellent low deposit formation. Moreover, when the test was modified by raising the test temperature from 275° F. to 350° F. at the end of 168 hours visual inspection of the samples showed that the Formulation A had far less deposit formation.
- Formulation A of Example 1 and a commercial lubricant composition (Comparative 3) were subjected to the ASTM-D 1401 demulsibility test. Comparative 3 was a PAO based lubricant containing 1.0 wt % of a polyalkylene dispersant. The results of the tests are shown in FIG. 3.
- As can be seen, Formulation A with the base stock of the invention showed complete water separation within 10 minutes. Formulation A, of course, did not contain a demulsfier additive.
- This example compares the oxidative and hydroytic stability, as determined by ASTM D 943 TOST life test, of two base stocks of the invention (A and B) with two other base stock (C and D). Base stock A comprised 80 wt % PAO (6 cSt at 100° C.); 10 wt % of an alkylated naphthalene (5 cSt at 100° C.) and 6 wt % an ester fluid (diisooctylphthalate). Base stock B differed from A in that the ester was a 50:50 mixture of ditridicyl phthalate and terephtalate ester.
- Base stock C and D used the same PAO as A and B. The alkylated aromatic fluid of C was the same as in A and B while the ester of D was a trimellitatte ester.
- The results of the tests are shown in FIG. 4.
- As can be seen A and
B display 30% longer life than C.
Claims (10)
1. A lubricant base stock blend comprising:
about 10 wt % or more of a polyalpha olefin (PAO) fluid;
about 1 wt % or more of an akylated aromatic fluid; and
about 1 wt % or more of an aromatic ester;
all amounts based on the weight of the blend.
2. The blend of claim 1 comprising:
from about 10 wt % to about 98 wt % of a PAO fluid;
from about 1 wt % to about 59 wt % of an alkylated aromatic fluid; and
from about 1 wt % to about 75 wt % of an aromatic ester.
3. The blend of claim 2 wherein the PAO comprise from about 80 to 85 wt %.
4. The blend of claim 2 wherein the alkylated aromatic comprises about 10 wt %.
5. The blend of claim 2 wherein the ester comprises from about 5 to about 8 wt %.
6. The blend of claim 1 or 2 wherein the alkylated aromatic is an alkylated naphthalene having 1 or more alkyl group of from 1 to about 8 carbon atoms.
7. The blend of claim 1 or 3 wherein the aromatic ester is the product of an aromatic acid or acid anhydride and a straight or branched aliphatic alcohol of from 3 to 18 carbon atoms.
8. The ester of claim 7 wherein the aromatic acid or anhyride is phthalic acid or anhydride.
9. A lubricant composition comprising:
a major amount of a lubricant base stock blend; and
an effective amount of at least one lubricant additive selected from the group consisting of antioxidants, rust inhibitors, extreme pressure agents, and metal deactivators;
the base stock blend comprising about 10 wt % or more of a polyalpha olefin fluid;
about 1 wt % or more of an alkylated aromatic fluid; and
about 1 wt % or more of an aromatic ester,
the amounts in the blend being based on the weight of the blend.
10. The composition of claim 9 wherein the blend comprises:
from about 10 wt % to about 98 wt % of a PAO fluid;
from about 1 wt % to about 59 wt % of an alkylated aromatic fluid; and
from about 1 wt % to about 75 wt % of an aromatic ester.
Priority Applications (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/292,096 US20030109389A1 (en) | 2001-11-30 | 2002-11-12 | Synthetic industrial oils made with "tri-synthetic" base stocks |
| EP02804433A EP1463791A1 (en) | 2001-11-30 | 2002-11-22 | Blends of three base oils and lubricating compositions based on them |
| AU2002365876A AU2002365876A1 (en) | 2001-11-30 | 2002-11-22 | Blends of three base oils and lubricating compositions based on them |
| CNA028238974A CN1596294A (en) | 2001-11-30 | 2002-11-22 | Mixture of three base oils and lubricating composition based thereon |
| JP2003549456A JP2005511815A (en) | 2001-11-30 | 2002-11-22 | Mixture of three base oils and lubricating oil composition based thereon |
| CA002467809A CA2467809A1 (en) | 2001-11-30 | 2002-11-22 | Blends of three base oils and lubricating compositions based on them |
| PCT/US2002/037490 WO2003048276A1 (en) | 2001-11-30 | 2002-11-22 | Blends of three base oils and lubricating compositions based on them |
| NO20042690A NO20042690D0 (en) | 2001-11-30 | 2004-06-25 | Mixtures of three base oils and lubricating compositions based thereon |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34005701P | 2001-11-30 | 2001-11-30 | |
| US10/292,096 US20030109389A1 (en) | 2001-11-30 | 2002-11-12 | Synthetic industrial oils made with "tri-synthetic" base stocks |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20030109389A1 true US20030109389A1 (en) | 2003-06-12 |
Family
ID=26967152
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/292,096 Abandoned US20030109389A1 (en) | 2001-11-30 | 2002-11-12 | Synthetic industrial oils made with "tri-synthetic" base stocks |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US20030109389A1 (en) |
| EP (1) | EP1463791A1 (en) |
| JP (1) | JP2005511815A (en) |
| CN (1) | CN1596294A (en) |
| AU (1) | AU2002365876A1 (en) |
| CA (1) | CA2467809A1 (en) |
| NO (1) | NO20042690D0 (en) |
| WO (1) | WO2003048276A1 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10351794B2 (en) * | 2014-12-12 | 2019-07-16 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
| US10731096B2 (en) * | 2015-08-21 | 2020-08-04 | Exxonmobil Chemical Patents Inc. | Lubricant base stock blends |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102433194B (en) * | 2011-10-21 | 2013-10-09 | 鞍山海华油脂化学有限公司 | Grease for motor bearings of wind generators and production method thereof |
| AU2015243391B2 (en) | 2014-04-11 | 2019-02-07 | Vgp Ipco Llc | Lubricant for preventing and removing carbon deposits in internal combustion engines |
| WO2015191421A1 (en) * | 2014-06-09 | 2015-12-17 | The Lubrizol Corporation | Synthetic industrial lubricants with improved compatibility |
| CN107325867A (en) * | 2017-06-20 | 2017-11-07 | 广州康尔克润滑油有限公司 | A kind of engine lubricating oil and preparation method thereof |
| CN108865356A (en) * | 2018-07-11 | 2018-11-23 | 王兴民 | The powerful anti-friction energy-saving petrol engine oil of one kind and its production technology |
| CN109762634A (en) * | 2019-01-21 | 2019-05-17 | 北京盛鑫和谐润滑油脂有限公司 | A kind of energy-saving diesel machine oil of overlength oil drain interval and preparation method thereof |
| CN109880680A (en) * | 2019-04-16 | 2019-06-14 | 江苏现代节能科技发展有限公司 | A kind of no phosphorous gasoline engine lubricant oil and preparation method thereof |
| CN119060775B (en) * | 2024-11-04 | 2025-01-24 | 烟台德高能源科技有限公司 | Energy-saving and long-life air compressor oil and preparation method thereof |
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|---|---|---|---|---|
| US4790957A (en) * | 1986-10-18 | 1988-12-13 | Basf Aktiengesellschaft | Polycarboxylic acid esters and lubricants containing these esters |
| US4967029A (en) * | 1989-09-07 | 1990-10-30 | Mobil Oil Corporation | Liquid lubricants from alpha-olefin and styrene copolymers |
| US5151205A (en) * | 1991-05-13 | 1992-09-29 | Texaco Inc. | Chain and drive gear lubricant |
| US5171904A (en) * | 1990-05-31 | 1992-12-15 | Texaco Chemical Company | Synthetic lubricant base stocks having an improved pour point |
| US5236610A (en) * | 1992-02-03 | 1993-08-17 | The United States Of America As Represented By The Secretary Of The Commerce | Stable high temperature liquid lubricant blends and antioxidant additives for use therewith |
| US5602086A (en) * | 1991-01-11 | 1997-02-11 | Mobil Oil Corporation | Lubricant compositions of polyalphaolefin and alkylated aromatic fluids |
| US5783528A (en) * | 1997-01-07 | 1998-07-21 | Diversey Lever, Inc. | Synthetic lubricant based on enhanced performance of synthetic ester fluids |
| US6235691B1 (en) * | 1997-11-12 | 2001-05-22 | Exxon Chemical Patents Inc. | Oil compositions with synthetic base oils |
| US6465400B1 (en) * | 1998-12-25 | 2002-10-15 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition for high-temperature use |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU661756B2 (en) * | 1992-02-18 | 1995-08-03 | Idemitsu Kosan Co. Ltd | Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane |
| US6713438B1 (en) * | 1999-03-24 | 2004-03-30 | Mobil Oil Corporation | High performance engine oil |
-
2002
- 2002-11-12 US US10/292,096 patent/US20030109389A1/en not_active Abandoned
- 2002-11-22 CA CA002467809A patent/CA2467809A1/en not_active Abandoned
- 2002-11-22 WO PCT/US2002/037490 patent/WO2003048276A1/en not_active Ceased
- 2002-11-22 EP EP02804433A patent/EP1463791A1/en not_active Withdrawn
- 2002-11-22 JP JP2003549456A patent/JP2005511815A/en active Pending
- 2002-11-22 CN CNA028238974A patent/CN1596294A/en active Pending
- 2002-11-22 AU AU2002365876A patent/AU2002365876A1/en not_active Abandoned
-
2004
- 2004-06-25 NO NO20042690A patent/NO20042690D0/en not_active Application Discontinuation
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4790957A (en) * | 1986-10-18 | 1988-12-13 | Basf Aktiengesellschaft | Polycarboxylic acid esters and lubricants containing these esters |
| US4967029A (en) * | 1989-09-07 | 1990-10-30 | Mobil Oil Corporation | Liquid lubricants from alpha-olefin and styrene copolymers |
| US5171904A (en) * | 1990-05-31 | 1992-12-15 | Texaco Chemical Company | Synthetic lubricant base stocks having an improved pour point |
| US5602086A (en) * | 1991-01-11 | 1997-02-11 | Mobil Oil Corporation | Lubricant compositions of polyalphaolefin and alkylated aromatic fluids |
| US5151205A (en) * | 1991-05-13 | 1992-09-29 | Texaco Inc. | Chain and drive gear lubricant |
| US5236610A (en) * | 1992-02-03 | 1993-08-17 | The United States Of America As Represented By The Secretary Of The Commerce | Stable high temperature liquid lubricant blends and antioxidant additives for use therewith |
| US5783528A (en) * | 1997-01-07 | 1998-07-21 | Diversey Lever, Inc. | Synthetic lubricant based on enhanced performance of synthetic ester fluids |
| US6235691B1 (en) * | 1997-11-12 | 2001-05-22 | Exxon Chemical Patents Inc. | Oil compositions with synthetic base oils |
| US6465400B1 (en) * | 1998-12-25 | 2002-10-15 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition for high-temperature use |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10351794B2 (en) * | 2014-12-12 | 2019-07-16 | Idemitsu Kosan Co., Ltd. | Lubricating oil composition |
| US10731096B2 (en) * | 2015-08-21 | 2020-08-04 | Exxonmobil Chemical Patents Inc. | Lubricant base stock blends |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2467809A1 (en) | 2003-06-12 |
| NO20042690L (en) | 2004-06-25 |
| WO2003048276A1 (en) | 2003-06-12 |
| EP1463791A1 (en) | 2004-10-06 |
| NO20042690D0 (en) | 2004-06-25 |
| JP2005511815A (en) | 2005-04-28 |
| AU2002365876A1 (en) | 2003-06-17 |
| CN1596294A (en) | 2005-03-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: EXXONMOBIL RESEARCH & ENGINEERING CO., NEW JERSEY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WARDLOW, ANDREA B.;REEL/FRAME:013395/0091 Effective date: 20030125 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |