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EP1463791A1 - Blends of three base oils and lubricating compositions based on them - Google Patents

Blends of three base oils and lubricating compositions based on them

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Publication number
EP1463791A1
EP1463791A1 EP02804433A EP02804433A EP1463791A1 EP 1463791 A1 EP1463791 A1 EP 1463791A1 EP 02804433 A EP02804433 A EP 02804433A EP 02804433 A EP02804433 A EP 02804433A EP 1463791 A1 EP1463791 A1 EP 1463791A1
Authority
EP
European Patent Office
Prior art keywords
blend
fluid
ester
pao
aromatic
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.)
Withdrawn
Application number
EP02804433A
Other languages
German (de)
French (fr)
Inventor
Andrea Blandford Wardlow
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
ExxonMobil Research and Engineering 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 ExxonMobil Research and Engineering Co filed Critical ExxonMobil Research and Engineering Co
Publication of EP1463791A1 publication Critical patent/EP1463791A1/en
Withdrawn legal-status Critical Current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
    • 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
    • C10M111/00Lubrication 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
    • C10M111/04Lubrication 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
    • 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
    • C10M2203/06Well-defined aromatic compounds
    • C10M2203/065Well-defined aromatic compounds used as base material
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/0206Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28Esters
    • C10M2207/285Esters of aromatic polycarboxylic acids
    • C10M2207/2855Esters of aromatic polycarboxylic acids used as base material
    • 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
    • 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
    • C10M2223/041Triaryl phosphates
    • 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
    • C10N2020/02Viscosity; Viscosity index
    • 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
    • C10N2030/04Detergent property or dispersant property
    • 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
    • C10N2030/10Inhibition of oxidation, e.g. anti-oxidants
    • 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
    • C10N2030/30Anti-misting
    • 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
    • C10N2030/66Hydrolytic 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 prepaied 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.
  • PAO base fluids provide 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.
  • polyol esters in PAO base fluids provides good dispersancy but poor hydrolytic stability.
  • one object of the present invention is to provide a lubricant product of improved dispersancy along with good demulsibility and hydrorytic 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:
  • Figure 1 is a graphic comparison of the storage stability of a commercial lubricant composition with one using a base stock of the invention.
  • Figure 2 graphically illustrates the deposit control property of a base stock of the invention.
  • Figure 3 graphically compaies the water demulsibility of a commercial composition with one using a base stock of the invention.
  • Figure 4 graphically compaies 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 industiial 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 or 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 ait. Those PAO's suitable in the practice of the present invention may be derived from C2 to about C32 alpha olefins with Cg to about C ⁇ _ 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 aiomatics and their method of preparation are well known in the ait. Suitable alkylated aiomatics are those having one or more short chain alkyl groups of from 1 to about 8 carbon atoms.
  • the preferred alkyl aiomatics will have viscosities in the range of about 3 cSt to about 300 cSt at 100°C.
  • the alkylated aiomatics 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 aiomatic ester fluid.
  • aiomatic ester fluid Common lubricant grade aiomatic 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 from 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 floe. Haze or floe, of course, is indicative of additive insolubility.
  • 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.
  • Figure 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 Macliine 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 Figure 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 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 Figure 3.
  • Formulation A with the base stock of the invention showed complete water sepaiation within 10 minutes. Fo ⁇ nulation A, of course, did not contain a demulsf ⁇ er additive.
  • This example compaies 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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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

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

BLENDS OF THREE BASE OILS AND LUBRICATING COMPOSITIONS BASED ON THEM
FIELD OF INVENTION
[0001] 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.
BACKGROUND OF INVENTION
[0002] Synthetic lubricant base stocks prepaied 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.
[0003] 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.
[0004] 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. [0005] The inclusion of polyol esters in PAO base fluids provides good dispersancy but poor hydrolytic stability.
[0006] Therefore, one object of the present invention is to provide a lubricant product of improved dispersancy along with good demulsibility and hydrorytic stability.
SUMMARY OF INVENTION
[0007] 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.
[0008] 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.
[0009] Advantageous features of the invention will become apparent from the detailed description that follows.
BRIEF DESCRIPTION OF DRAWINGS
[0010] Figure 1 is a graphic comparison of the storage stability of a commercial lubricant composition with one using a base stock of the invention. [0011] Figure 2 graphically illustrates the deposit control property of a base stock of the invention.
[0012] Figure 3 graphically compaies the water demulsibility of a commercial composition with one using a base stock of the invention.
[0013] Figure 4 graphically compaies the oxidative and hydrolytic stability of two base stocks formulations of the invention with two others.
DETAILED DESCRIPTION OF INVENTION
[0014] 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 industiial 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 or moisture ingress such as oils used in combined cycle turbines, paper machinery, rod mills and the like.
[0015] 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%. [0016] PAO fluids and their preparation are well known in the ait. Those PAO's suitable in the practice of the present invention may be derived from C2 to about C32 alpha olefins with Cg to about C\ _ 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.
[0017] 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 aiomatics and their method of preparation are well known in the ait. Suitable alkylated aiomatics are those having one or more short chain alkyl groups of from 1 to about 8 carbon atoms. The preferred alkyl aiomatics will have viscosities in the range of about 3 cSt to about 300 cSt at 100°C. The alkylated aiomatics 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%.
[0018] The base stock of the present invention also includes an aiomatic ester fluid. Common lubricant grade aiomatic 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 from 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. [0019] 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.
[0020] The following examples and comparative examples fui her illustrate the many advantageous of the instant invention.
EXAMPLES
Example 1
[0021] 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 floe. Haze or floe, of course, is indicative of additive insolubility. [0022] 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.
[0023] Figure 1 graphically presents the results of the tests and illustrates the improved solubility that the base stock of the invention has for lubricant additives.
Example 2
[0024] 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 Macliine 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 Figure 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
[0025] 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 Figure 3. [0026] As can be seen, Formulation A with the base stock of the invention showed complete water sepaiation within 10 minutes. Foπnulation A, of course, did not contain a demulsfϊer additive.
Example 4
[0027] This example compaies 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.
[0028] 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.
[0029] The results of the tests are shown in Figure 4.
[0030] As can be seen A and B display 30% longer life than C.

Claims

CLAIMS:
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 aiomatic fluid; and
about 1 wt% or more of an aiomatic 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 aiomatic 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 aiomatic 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 aiomatic acid or acid anhydiide and a stiaight 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 anhydiide.
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 pressme 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 aiomatic 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.
EP02804433A 2001-11-30 2002-11-22 Blends of three base oils and lubricating compositions based on them Withdrawn EP1463791A1 (en)

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US34005701P 2001-11-30 2001-11-30
US340057P 2001-11-30
US292096 2002-11-12
US10/292,096 US20030109389A1 (en) 2001-11-30 2002-11-12 Synthetic industrial oils made with "tri-synthetic" base stocks
PCT/US2002/037490 WO2003048276A1 (en) 2001-11-30 2002-11-22 Blends of three base oils and lubricating compositions based on them

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Families Citing this family (10)

* Cited by examiner, † Cited by third party
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
MX2016013333A (en) * 2014-04-11 2017-05-01 Valvoline Licensing & Intellectual Property LLC Lubricant for preventing and removing carbon deposits in internal combustion engines.
SG10201810920UA (en) 2014-06-09 2019-01-30 Lubrizol Corp Synthetic industrial lubricants with improved compatibility
JP5941972B2 (en) * 2014-12-12 2016-06-29 出光興産株式会社 Lubricating oil composition
CN108026466B (en) * 2015-08-21 2021-10-22 埃克森美孚化学专利公司 Lubricant Basestock Blends
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

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3635490A1 (en) * 1986-10-18 1988-04-21 Basf Ag USE OF POLYCARBONIC ACID ESTERS IN FULL OR PART SYNTHETIC LUBRICANTS 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
DK0496486T3 (en) * 1991-01-11 1994-03-28 Mobil Oil Corp Lubricant Compositions
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
AU661756B2 (en) * 1992-02-18 1995-08-03 Idemitsu Kosan Co. Ltd Lubricant for refrigerating machine employing refrigerant comprising tetrafluoroethane
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
JP4049916B2 (en) * 1998-12-25 2008-02-20 出光興産株式会社 High temperature lubricating oil composition
US6713438B1 (en) * 1999-03-24 2004-03-30 Mobil Oil Corporation High performance engine oil

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO03048276A1 *

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CN1596294A (en) 2005-03-16
WO2003048276A1 (en) 2003-06-12
CA2467809A1 (en) 2003-06-12
US20030109389A1 (en) 2003-06-12
NO20042690D0 (en) 2004-06-25
AU2002365876A1 (en) 2003-06-17
NO20042690L (en) 2004-06-25
JP2005511815A (en) 2005-04-28

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