US20090054285A1 - Lubricant composition with low deposition tendency - Google Patents
Lubricant composition with low deposition tendency Download PDFInfo
- Publication number
- US20090054285A1 US20090054285A1 US12/229,161 US22916108A US2009054285A1 US 20090054285 A1 US20090054285 A1 US 20090054285A1 US 22916108 A US22916108 A US 22916108A US 2009054285 A1 US2009054285 A1 US 2009054285A1
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- United States
- Prior art keywords
- base oil
- group iii
- blend
- cycloparaffins
- oil
- Prior art date
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- Abandoned
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- 239000000203 mixture Substances 0.000 title claims abstract description 56
- 239000000314 lubricant Substances 0.000 title abstract description 9
- 230000008021 deposition Effects 0.000 title abstract description 3
- 239000002199 base oil Substances 0.000 claims abstract description 63
- 230000001050 lubricating effect Effects 0.000 claims abstract description 8
- 239000002272 engine oil additive Substances 0.000 claims abstract description 4
- 239000003921 oil Substances 0.000 claims description 36
- 239000002270 dispersing agent Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 239000003963 antioxidant agent Substances 0.000 claims description 8
- -1 VI improvers Substances 0.000 claims description 6
- 239000003599 detergent Substances 0.000 claims description 5
- 239000010705 motor oil Substances 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000003112 inhibitor Substances 0.000 claims description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 4
- 239000003607 modifier Substances 0.000 claims description 4
- 239000010687 lubricating oil Substances 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims 1
- 229920013639 polyalphaolefin Polymers 0.000 description 10
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 229960002317 succinimide Drugs 0.000 description 4
- 239000001993 wax Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000003879 lubricant additive Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002530 phenolic antioxidant Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- ROGIWVXWXZRRMZ-UHFFFAOYSA-N 2-methylbuta-1,3-diene;styrene Chemical compound CC(=C)C=C.C=CC1=CC=CC=C1 ROGIWVXWXZRRMZ-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007866 anti-wear additive Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 125000005028 dihydroxyaryl group Chemical group 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
Classifications
-
- 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
-
- 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
-
- 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
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/106—Naphthenic fractions
- C10M2203/1065—Naphthenic fractions 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
- C10M2205/17—Fisher Tropsch reaction products
- C10M2205/173—Fisher Tropsch reaction products used as base material
-
- 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
Definitions
- the present invention relates to blended lubricant base oils useful in formulating engine oil lubricant compositions having low deposition and varnish-forming tendency.
- Lubricating compositions for use in internal combustion engines typically comprise a base oil and a variety of additives to enhance the performance characteristics of the base oil.
- Important performance characteristics of a base oil include oxidation stability, additive solubility and deposit control. Because the base oil is the major constituent in these lubricating compositions, it contributes significantly to the properties of the finished lubricant.
- lubricant manufacturers are seeking base oils that have better performance characteristics than many petroleum derived base oils presently used in lubricating compositions.
- synthetic base oils such as polyalphaolefins (PAOs) that have better oxidation stability, for example, than petroleum derived base oils.
- PAO base oils are produced by a chemical polymerization process.
- F-T Fischer-Tropsch
- PAOs exhibit good oxidation stability and deposit control, they have poor additive solubility and are expensive to produce.
- Fischer-Tropsch (F-T) derived lubricant base oils are desirable for their oxidation stability biodegradability and low levels of undesirable impurities, such as sulfur.
- F-T base oils are less expensive to produce than PAOs, F-T oils do not exhibit the same deposit control properties as PAOs. It would be useful, therefore, to provide a base oil comprising an F-T base oil that exhibits good deposit control.
- a lubricant base oil blend consisting essentially from about 20 wt % to about 80 wt %, based on the total weight of the blend, of an F-T Group III base oil containing less than 5 wt % cycloparaffins, the balance of the blend being a Group III base oil containing at least 35 wt % cycloparaffins.
- an engine oil composition comprising: a major amount of a base oil blend consisting essentially of 20 wt % to about 80 wt % of an F-T Group III base oil having less than 5 wt % cycloparaffins and the balance being a Group III base oil having at least 30 wt % cycloparaffins; and at least one engine oil additive selected from dispersants, detergents, antiwear agents, VI improvers, antioxidants, defoamants, friction modifiers and rust inhibitors.
- the F-T Group III oils used in the present invention are derived from synthesis gas in the F-T hydrocarbon synthesis process.
- the other Group III oils used in the base oil blends of the invention may be derived from natural petroleum base stocks.
- the F-T Group III oils used in the base oil blends are characterized as having less than 5 wt % cycloparaffins, for example, from about 0.5 wt % to about 4.75 wt % where the mono to cycloparaffins ratio is 10/1 or greater.
- the F-T Group III oil will have a kinematic viscosity in the range of about 2.0 to 8.0 mm 2 /s at 100° C. and preferably in the range of about 3.5 to 6.5 at 100° C.
- the F-T Group III oils used in the present invention have predominantly paraffinic components.
- the F-T Group III oils have less than 0.1 wt % aromatic hydrocarbons, less than 20 wppm nitrogen-containing compounds and less than 20 wppm sulfur-containing compounds. These F-T oils typically have an initial boiling point of about 345° C.
- the F-T Group III oils used in the invention have a pour point lower than ⁇ 18° C. preferably lower than ⁇ 21° C.
- the F-T Group III oils are prepared by catalytically converting a synthesis gas comprising a mixture of H 2 and CO into hydrocarbons, usually waxy hydrocarbons (referred to as F-T wax).
- F-T wax is then converted to lower boiling material by processes comprising hydroisomerization and hydrotreating. These processes are all well known by persons of ordinary skill in the art.
- the process of making a lubricant F-T Group III base oil from an F-T wax may include preliminary treatment to remove oxygenates. Treatment to remove any sulfur and nitrogen compounds is not normally needed because F-T waxes have only trace amounts of sulfur or nitrogen.
- the base oil blend of the invention consists essentially of from about 20 wt % to about 80 wt %, preferably from 30 wt % to 80 wt % and more preferably 50 wt % to 80 wt % of an F-T Group III oil having less than 5 wt % cycloparaffins.
- the balance (i.e., about 80 wt % to about 20 wt %) of the base oil blend of the invention consists of a Group III oil having at least 35 wt % cycloparaffins, preferably from 40 wt % to about 50 wt % and more preferably from about 44 wt % to 50 wt %.
- Group III oils typically are derived from natural petroleum base stocks and are commercially available materials. Typically, they will have a kinematic viscosity in the range of about 3.5 mm 2 /s to about 6.5 mm 2 /s at 100° C.
- These Group III oils will have a nominal initial boiling point of about 365° C. and a pour point lower than ⁇ 18° C. and preferably lower than ⁇ 21° C.
- the base oil blends of the invention are particularly suitable for use in preparing lubricating oils for internal combustion engines. They may be formulated to have a single viscosity grade, such as SAE 30. Preferably, the base oil blends are formulated with VI improvers that provide the composition with a multi-viscosity grade such as 5W30 and 5W40 grades.
- an engine oil lubricating composition comprising: a major amount of a base oil blend consisting essentially of 20 wt % to about 80 wt % of an F-T Group III base oil having less than 5 wt % cycloparaffins and the balance being a Group III base oil having at least 30 wt % cycloparaffins; and at least one engine oil additive selected from dispersants, detergents, antiwear agents, VI improvers, antioxidants, defoamants, friction modifiers and rust inhibitors.
- Suitable dispersants include succinimide dispersants, ester dispersants, ester-amide dispersants, and the like.
- the dispersant is a succinimide dispersant, especially a polybutenyl succinimide.
- the molecular weight of the polybutenyl group may range from about 800 to about 4000 or more and preferably from about 1300 to about 2500.
- the dispersant may be head capped or borated or both.
- useful detergents are the alkali and alkaline earth metal salicylates, alkylsalicylates, phenates and sulfonates.
- a commonly used class of antiwear additives is zinc dialkyldithiophosphates in which the alkyl groups typically have from 3 to about 18 carbon atoms with 3 to 10 carbon atoms being preferred.
- Suitable VI improvers include linear or radial styrene-isoprene VI improvers, olefin copolymers, polymethacrylates, and the like.
- suitable antioxidants include aminic antioxidants and phenolic antioxidants. Typical aminic antioxidants include alkylated aromatic amines, especially those in which the alkyl group contains no more than 14 carbon atoms.
- Typical phenolic antioxidants include derivatives of dihydroxy aryl compounds in which the hydroxyl groups are in the o- or p-position to each other and which contain alkyl substituents. Mixtures of phenolic and aminic antioxidants also may be used. Such antioxidant(s) may be used in an amount of about 0.02 to 5 wt % and preferably about 0.1 wt % to about 2 wt % based on the total weight of the composition.
- Suitable antifoam additives include silicone oils or polysiloxane oils usually used in amounts of from 0.0001 to 0.01 wt % active ingredient.
- Pour point depressants are well known lubricant additives. Typical examples are dialkylfumarates, polyalkylmethacrylates, and the like.
- the number and types of friction modifiers are voluminous. In general, they include metal salts of fatty acids, glycerol esters and alkoxylated fatty amines to mention a few.
- Rust inhibitors selected from the group consisting of nonionic polyoxyalkylene polyols and esters thereof, polyoxyalkylene phenols and aminic alkyl sulfonic acids may be used.
- the various lubricant additives will comprise from about 0.5 wt % to about 25 wt % and preferably from about 2 wt % to about 10 wt % based on the total weight of the composition.
- Each formulation contained the same commercially available additive package (adpack).
- the adpack contained a non-borated PIB succinimide dispersant, calcium and magnesium detergent, zinc alkyldithiophosphate antiwear agent, and a polydimethylsilicone antifoamant.
- the oils were formulated to a target kinematic viscosity at 100° C. of about 14 mm 2 /s.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Lubricant base oil blends and finished lubricating compositions having low deposition tendency are provided. The base oil blends consist essentially of about 20 wt % to about 80 wt %, based on the total weight of the blend, of an F-T Group III base oil having less than 5 wt % cycloparaffins, the balance of the blend being a Group III base oil having at least 35 wt % cycloparaffins. The finished lubricating compositions comprise a major amount of the base oil blend of the invention and at least one engine oil additive.
Description
- This application claims benefit of Provisional Application 60/965,598 filed Aug. 21, 2007.
- The present invention relates to blended lubricant base oils useful in formulating engine oil lubricant compositions having low deposition and varnish-forming tendency.
- Lubricating compositions for use in internal combustion engines typically comprise a base oil and a variety of additives to enhance the performance characteristics of the base oil. Important performance characteristics of a base oil include oxidation stability, additive solubility and deposit control. Because the base oil is the major constituent in these lubricating compositions, it contributes significantly to the properties of the finished lubricant. To produce high performance lubricating compositions, lubricant manufacturers are seeking base oils that have better performance characteristics than many petroleum derived base oils presently used in lubricating compositions. Thus, there is a trend toward using synthetic base oils such as polyalphaolefins (PAOs) that have better oxidation stability, for example, than petroleum derived base oils. PAO base oils are produced by a chemical polymerization process. Although PAOs exhibit good oxidation stability and deposit control, they have poor additive solubility and are expensive to produce. Fischer-Tropsch (F-T) derived lubricant base oils are desirable for their oxidation stability biodegradability and low levels of undesirable impurities, such as sulfur. Although F-T base oils are less expensive to produce than PAOs, F-T oils do not exhibit the same deposit control properties as PAOs. It would be useful, therefore, to provide a base oil comprising an F-T base oil that exhibits good deposit control.
- Accordingly, in one embodiment of the present invention, there is provided a lubricant base oil blend consisting essentially from about 20 wt % to about 80 wt %, based on the total weight of the blend, of an F-T Group III base oil containing less than 5 wt % cycloparaffins, the balance of the blend being a Group III base oil containing at least 35 wt % cycloparaffins. In another embodiment of the invention, there is provided an engine oil composition comprising: a major amount of a base oil blend consisting essentially of 20 wt % to about 80 wt % of an F-T Group III base oil having less than 5 wt % cycloparaffins and the balance being a Group III base oil having at least 30 wt % cycloparaffins; and at least one engine oil additive selected from dispersants, detergents, antiwear agents, VI improvers, antioxidants, defoamants, friction modifiers and rust inhibitors.
- As is well known, the American Petroleum Institute has established a classification system for base oils (API Publication 1509, www.API.org). Group III oils are one of the five categories established by the API. The properties of all five categories are shown in Table 1.
-
TABLE 1 Saturates Sulfur Viscosity Index Group I <90% and/or >0.03% and ≧80 and <120 Group II ≧90% and ≦0.03% and ≧80 and <120 Group III ≧90% and ≦0.03% and ≧120 Group IV Polyalphaolefins (PAO) Group V All other base oil stocks not included in Groups I, II, III, or IV - The F-T Group III oils used in the present invention are derived from synthesis gas in the F-T hydrocarbon synthesis process. The other Group III oils used in the base oil blends of the invention may be derived from natural petroleum base stocks.
- The F-T Group III oils used in the base oil blends are characterized as having less than 5 wt % cycloparaffins, for example, from about 0.5 wt % to about 4.75 wt % where the mono to cycloparaffins ratio is 10/1 or greater. Typically, the F-T Group III oil will have a kinematic viscosity in the range of about 2.0 to 8.0 mm2/s at 100° C. and preferably in the range of about 3.5 to 6.5 at 100° C.
- The F-T Group III oils used in the present invention have predominantly paraffinic components. Preferably, the F-T Group III oils have less than 0.1 wt % aromatic hydrocarbons, less than 20 wppm nitrogen-containing compounds and less than 20 wppm sulfur-containing compounds. These F-T oils typically have an initial boiling point of about 345° C. The F-T Group III oils used in the invention have a pour point lower than −18° C. preferably lower than −21° C.
- The F-T Group III oils are prepared by catalytically converting a synthesis gas comprising a mixture of H2 and CO into hydrocarbons, usually waxy hydrocarbons (referred to as F-T wax). The F-T wax is then converted to lower boiling material by processes comprising hydroisomerization and hydrotreating. These processes are all well known by persons of ordinary skill in the art.
- The process of making a lubricant F-T Group III base oil from an F-T wax may include preliminary treatment to remove oxygenates. Treatment to remove any sulfur and nitrogen compounds is not normally needed because F-T waxes have only trace amounts of sulfur or nitrogen.
- Particularly favorable processes that can be used for the production of F-T Group III oils are described in U.S. Pat. Nos. 4,594,172; 4,943,672; 6,046,940; 6,475,960; 6,103,099; 6,332,974 and 6,375,830, all incorporated herein by reference.
- The base oil blend of the invention consists essentially of from about 20 wt % to about 80 wt %, preferably from 30 wt % to 80 wt % and more preferably 50 wt % to 80 wt % of an F-T Group III oil having less than 5 wt % cycloparaffins.
- The balance (i.e., about 80 wt % to about 20 wt %) of the base oil blend of the invention consists of a Group III oil having at least 35 wt % cycloparaffins, preferably from 40 wt % to about 50 wt % and more preferably from about 44 wt % to 50 wt %. Such Group III oils typically are derived from natural petroleum base stocks and are commercially available materials. Typically, they will have a kinematic viscosity in the range of about 3.5 mm2/s to about 6.5 mm2/s at 100° C. These Group III oils will have a nominal initial boiling point of about 365° C. and a pour point lower than −18° C. and preferably lower than −21° C.
- The base oil blends of the invention are particularly suitable for use in preparing lubricating oils for internal combustion engines. They may be formulated to have a single viscosity grade, such as SAE 30. Preferably, the base oil blends are formulated with VI improvers that provide the composition with a multi-viscosity grade such as 5W30 and 5W40 grades. Thus, one embodiment of the invention provides an engine oil lubricating composition comprising: a major amount of a base oil blend consisting essentially of 20 wt % to about 80 wt % of an F-T Group III base oil having less than 5 wt % cycloparaffins and the balance being a Group III base oil having at least 30 wt % cycloparaffins; and at least one engine oil additive selected from dispersants, detergents, antiwear agents, VI improvers, antioxidants, defoamants, friction modifiers and rust inhibitors.
- Suitable dispersants include succinimide dispersants, ester dispersants, ester-amide dispersants, and the like. Preferably, the dispersant is a succinimide dispersant, especially a polybutenyl succinimide. The molecular weight of the polybutenyl group may range from about 800 to about 4000 or more and preferably from about 1300 to about 2500. The dispersant may be head capped or borated or both.
- Examples of useful detergents are the alkali and alkaline earth metal salicylates, alkylsalicylates, phenates and sulfonates.
- A commonly used class of antiwear additives is zinc dialkyldithiophosphates in which the alkyl groups typically have from 3 to about 18 carbon atoms with 3 to 10 carbon atoms being preferred. Suitable VI improvers include linear or radial styrene-isoprene VI improvers, olefin copolymers, polymethacrylates, and the like. Examples of suitable antioxidants include aminic antioxidants and phenolic antioxidants. Typical aminic antioxidants include alkylated aromatic amines, especially those in which the alkyl group contains no more than 14 carbon atoms. Typical phenolic antioxidants include derivatives of dihydroxy aryl compounds in which the hydroxyl groups are in the o- or p-position to each other and which contain alkyl substituents. Mixtures of phenolic and aminic antioxidants also may be used. Such antioxidant(s) may be used in an amount of about 0.02 to 5 wt % and preferably about 0.1 wt % to about 2 wt % based on the total weight of the composition.
- Suitable antifoam additives include silicone oils or polysiloxane oils usually used in amounts of from 0.0001 to 0.01 wt % active ingredient. Pour point depressants are well known lubricant additives. Typical examples are dialkylfumarates, polyalkylmethacrylates, and the like.
- The number and types of friction modifiers are voluminous. In general, they include metal salts of fatty acids, glycerol esters and alkoxylated fatty amines to mention a few.
- Rust inhibitors selected from the group consisting of nonionic polyoxyalkylene polyols and esters thereof, polyoxyalkylene phenols and aminic alkyl sulfonic acids may be used.
- In general, on an active ingredient basis, the various lubricant additives will comprise from about 0.5 wt % to about 25 wt % and preferably from about 2 wt % to about 10 wt % based on the total weight of the composition.
- A series of oils were formulated using the base oils and base oil blends shown in Table 2. The cycloparaffin content shown in Table 2 was determined by the Brandes Infra Red Method (see Brandes G., Brennstoff-Chem, 37, 1956, pages 263-267).
- Each formulation contained the same commercially available additive package (adpack). The adpack contained a non-borated PIB succinimide dispersant, calcium and magnesium detergent, zinc alkyldithiophosphate antiwear agent, and a polydimethylsilicone antifoamant.
- The oils were formulated to a target kinematic viscosity at 100° C. of about 14 mm2/s.
- The deposit tendency of each of the formulated oils was determined by the MHT-4 test, ASTM D7097. The results of the test are given in Table 2.
-
TABLE 2 Oil 1 Oil 2 Oil 3 Oil 4 Oil 5 Oil 6 Oil 7 5W-40 5W-40 5W-40 5W-40 5W-40 5W-40 5W-40 Base Oil, wt % F-T III 67.2 47.9 46.2 47.8 Group III - Source A 67.2 19.6 Group III - Source B 67.2 21.3 PAO 67.2 19.7 Adpack, wt % 13.8 13.8 13.8 13.8 13.7 13.7 13.7 VI Improver, wt % (1) 19.0 19.0 19.0 19.0 18.8 18.8 18.8 Cycloparaffins, wt % 4.7 31.0 44.4 4.7 9.8 13.2 4.7 Properties KV @ 40° C., mm2/s 79.4 82.4 92.6 83.4 79.3 83.5 80.2 KV @ 100° C., mm2/s 14.0 14.3 15.0 13.9 14.1 14.5 14.1 MTH-4, Deposits, mg 75.8 50.3 48.4 39.4 83.7 58.9 79.9 Calc. MHT-4 Deposits, mg — — — — 68.7 67.5 65.5 (1) 6 wt % in mineral oil. Source A = Visom Source B = Yubase - The results in Table 2 show that Oil 6 of this invention gave unexpectedly lower deposits than the calculated GTL and PAO base oils combination (Oil 7). The results could not be predicted since Oil 7 was expected to give the lowest deposits.
- For each of Oils 5, 6 and 7, the amount of deposits that could be expected was calculated using the MTH-4 deposits produced by each oil and the ratio of the base oils used in the blends. A comparison of the calculated results with the actual results shows that the deposit-forming tendency is not predictable. Also, the results show that Oil 6 of the invention gave unexpectedly lower deposits than Oil 7, which would be expected to give lower deposits.
Claims (14)
1. A lubricating base oil blend consisting essentially of from about 20 wt % to about 80 wt %, based on the total weight of the blend, of an F-T Group III base oil having less than 5 wt % cycloparaffins, the balance being a Group III base oil having at least 35 wt % cycloparaffins.
2. The blend of claim 1 wherein the F-T Group III base oil comprises 30 wt % to 80 wt % of the blend.
3. The blend of claim 2 wherein the F-T Group III base oil comprises 50 wt % to 80 wt % of the blend.
4. The blend of claim 3 wherein the Group III base oil has from 40 wt % to 50 wt % of cycloparaffins.
5. The blend of claim 4 wherein the Group III base oil has from about 44 wt % to about 50 wt % of cycloparaffins.
6. A lubricating oil composition comprising:
a major amount of a base oil blend consisting essentially of about 20 wt % to about 80 wt %, based on the total weight of the blend, of an F-T Group III base oil having less than 5 wt % cycloparaffins, the balance of the blend being a Group III base oil having at least 35 wt % cycloparaffins, and
at least one engine oil additive selected from dispersants, detergents, antiwear agents, VI improvers, antioxidants, defoamants, friction modifiers and rust inhibitors.
7. The composition of claim 6 wherein the F-T Group III base oil comprises 30 wt % to 80 wt % of the blend.
8. The composition of claim 7 wherein the F-T Group III base oil comprises 50 wt % to 80 wt % of the blend.
9. The composition of claim 8 wherein the Group III base oil has from 35 wt % to 50 wt % of cycloparaffins.
10. The composition of claim 9 wherein the Group III base oil has from about 40 wt % to about 50 wt % of cycloparaffins.
11. A method for improving the deposit control as measured by test MTH-4 (ASTM D7097) of a fully formulated engine oil comprising an F-T Group III base oil having less than 5 wt % cycloparaffins, the method comprising blending the F-T Group III base oil with a sufficient amount of a Group III base oil having at least 35 wt % cycloparaffins to provide the blend with from about 20 wt % to about 80 wt %, based on the total weight of the blend, of the F-T Group III oil.
12. The method of claim 11 wherein the Group III base oil has from about 40 wt % to about 50 wt % of cycloparaffins.
13. The method of claim 12 wherein the amount of Group III oil is sufficient to provide a blend with from 30 wt % to 80 wt % of the F-T Group III base oil.
14. Use of the base oil blend of any one of claims 1 to 5 as the base oil in a fully formulated engine oil.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/229,161 US20090054285A1 (en) | 2007-08-21 | 2008-08-20 | Lubricant composition with low deposition tendency |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96559807P | 2007-08-21 | 2007-08-21 | |
| US12/229,161 US20090054285A1 (en) | 2007-08-21 | 2008-08-20 | Lubricant composition with low deposition tendency |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20090054285A1 true US20090054285A1 (en) | 2009-02-26 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12/229,161 Abandoned US20090054285A1 (en) | 2007-08-21 | 2008-08-20 | Lubricant composition with low deposition tendency |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20090054285A1 (en) |
| EP (1) | EP2193185A2 (en) |
| CA (1) | CA2697030A1 (en) |
| SG (2) | SG10201706802TA (en) |
| WO (1) | WO2009025844A2 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9127229B2 (en) * | 2009-07-24 | 2015-09-08 | Cherron Oronite Technology B.V. | Trunk piston engine lubricating oil compositions |
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| US20030088133A1 (en) * | 2001-10-19 | 2003-05-08 | O'rear Dennis J. | Lube base oils with improved yield |
| US20040067856A1 (en) * | 2002-10-08 | 2004-04-08 | Johnson Jack Wayne | Synthetic isoparaffinic premium heavy lubricant base stock |
| US6730638B2 (en) * | 2002-01-31 | 2004-05-04 | Exxonmobil Research And Engineering Company | Low ash, low phosphorus and low sulfur engine oils for internal combustion engines |
| US20050261147A1 (en) * | 2004-05-19 | 2005-11-24 | Chevron U.S.A. Inc. | Lubricant blends with low brookfield viscosities |
| US20050261145A1 (en) * | 2004-05-19 | 2005-11-24 | Chevron U.S.A. Inc. | Lubricant blends with low brookfield viscosities |
| US20050258078A1 (en) * | 2004-05-19 | 2005-11-24 | Chevron U.S.A. Inc. | Processes for making lubricant blends with low brookfield viscosities |
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| US20060199743A1 (en) * | 2005-03-03 | 2006-09-07 | Chevron U.S.A. Inc. | Polyalphaolefin & fischer-tropsch derived lubricant base oil lubricant blends |
| US20060289337A1 (en) * | 2003-12-23 | 2006-12-28 | Chevron U.S.A. Inc. | Process for making lubricating base oils with high ratio of monocycloparaffins to multicycloparaffins |
| US20070232503A1 (en) * | 2006-03-31 | 2007-10-04 | Haigh Heather M | Soot control for diesel engine lubricants |
| US20100035777A1 (en) * | 2005-01-07 | 2010-02-11 | Takashi Sano | Lubricant base oil, lubricant composition for internal combustion engine and lubricant composition for driving force transmitting device |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE302258T1 (en) * | 2001-02-13 | 2005-09-15 | Shell Int Research | LUBRICANT OIL COMPOSITION |
| WO2005000999A1 (en) * | 2003-06-27 | 2005-01-06 | Shell Internationale Research Maatschappij B.V. | Process to prepare a lubricating base oil |
| US20090159492A1 (en) * | 2004-12-24 | 2009-06-25 | Etienne Duhoux | Process to prepare a lubricating base oil and its use |
-
2008
- 2008-08-20 US US12/229,161 patent/US20090054285A1/en not_active Abandoned
- 2008-08-21 CA CA2697030A patent/CA2697030A1/en not_active Abandoned
- 2008-08-21 SG SG10201706802TA patent/SG10201706802TA/en unknown
- 2008-08-21 EP EP08795504A patent/EP2193185A2/en not_active Withdrawn
- 2008-08-21 SG SG2012062485A patent/SG183764A1/en unknown
- 2008-08-21 WO PCT/US2008/009970 patent/WO2009025844A2/en active Application Filing
Patent Citations (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030088133A1 (en) * | 2001-10-19 | 2003-05-08 | O'rear Dennis J. | Lube base oils with improved yield |
| US6730638B2 (en) * | 2002-01-31 | 2004-05-04 | Exxonmobil Research And Engineering Company | Low ash, low phosphorus and low sulfur engine oils for internal combustion engines |
| US20040067856A1 (en) * | 2002-10-08 | 2004-04-08 | Johnson Jack Wayne | Synthetic isoparaffinic premium heavy lubricant base stock |
| US20060289337A1 (en) * | 2003-12-23 | 2006-12-28 | Chevron U.S.A. Inc. | Process for making lubricating base oils with high ratio of monocycloparaffins to multicycloparaffins |
| US20050261147A1 (en) * | 2004-05-19 | 2005-11-24 | Chevron U.S.A. Inc. | Lubricant blends with low brookfield viscosities |
| US20050261145A1 (en) * | 2004-05-19 | 2005-11-24 | Chevron U.S.A. Inc. | Lubricant blends with low brookfield viscosities |
| US20050258078A1 (en) * | 2004-05-19 | 2005-11-24 | Chevron U.S.A. Inc. | Processes for making lubricant blends with low brookfield viscosities |
| US20100035777A1 (en) * | 2005-01-07 | 2010-02-11 | Takashi Sano | Lubricant base oil, lubricant composition for internal combustion engine and lubricant composition for driving force transmitting device |
| US20060196807A1 (en) * | 2005-03-03 | 2006-09-07 | Chevron U.S.A. Inc. | Polyalphaolefin & Fischer-Tropsch derived lubricant base oil lubricant blends |
| US20060199743A1 (en) * | 2005-03-03 | 2006-09-07 | Chevron U.S.A. Inc. | Polyalphaolefin & fischer-tropsch derived lubricant base oil lubricant blends |
| US20070232503A1 (en) * | 2006-03-31 | 2007-10-04 | Haigh Heather M | Soot control for diesel engine lubricants |
Also Published As
| Publication number | Publication date |
|---|---|
| SG10201706802TA (en) | 2017-10-30 |
| WO2009025844A2 (en) | 2009-02-26 |
| EP2193185A2 (en) | 2010-06-09 |
| WO2009025844A3 (en) | 2009-05-14 |
| SG183764A1 (en) | 2012-09-27 |
| CA2697030A1 (en) | 2009-02-26 |
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