US2996455A - High viscosity index, low viscosity, low volatility motor oil - Google Patents
High viscosity index, low viscosity, low volatility motor oil Download PDFInfo
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- US2996455A US2996455A US631064A US63106456A US2996455A US 2996455 A US2996455 A US 2996455A US 631064 A US631064 A US 631064A US 63106456 A US63106456 A US 63106456A US 2996455 A US2996455 A US 2996455A
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G31/00—Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for
- C10G31/06—Refining of hydrocarbon oils, in the absence of hydrogen, by methods not otherwise provided for by heating, cooling, or pressure treatment
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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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with 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
- 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
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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
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
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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
- 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
- C10M2205/026—Butene
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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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/04—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing aromatic monomers, e.g. styrene
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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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
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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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/022—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group
- C10M2217/023—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an amino group the amino group containing an ester bond
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/14—Electric or magnetic purposes
- C10N2040/17—Electric or magnetic purposes for electric contacts
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/30—Refrigerators lubricants or compressors lubricants
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/32—Wires, ropes or cables lubricants
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/34—Lubricating-sealants
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/36—Release agents or mold release agents
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/38—Conveyors or chain belts
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/40—Generators or electric motors in oil or gas winning field
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/42—Flashing oils or marking oils
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—Super vacuum or supercritical use
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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
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/50—Medical uses
Definitions
- This invention relates to oil compositions that are useful primarily as engine lubricating oils and are characterized by a unique and most desirable combination of high viscosity index, low viscosity at low temperatures and low volatility at higher temperatures.
- oils are generally oils or oil blends containing at least about 8% and as much as 15% by volume of one or more high molecular weight polymers, e.g., polybutenes, well known in the industry as viscosity index improvers. It is possible, for example, to blend enough of a viscosity index improver with an oil having a viscosity index of say 100 to increase its viscosity index to 140 or more and thus make it eligible for classification as a triple branded motor oil such as SAE W-20.
- Blends of thicker oil with the same amount of viscosity index improver had reduced volatility at the higher temperature and therefore better consumption characteristics, but were too viscous at low starting temperatures.
- the use of lesser amounts of viscosity improver with thicker oils can result in acceptable values of viscosity at starting temperatures and volatility at engine operating temperatures, but results in a reduction of viscosity at engine operating temperatures to a point that is inadequate for proper lubrication under the conditions of operation.
- an oil composition having all three desirable attributes of low low-temperature viscosity, high high-temperature viscosity (i.e., high viscosity index) and low volatility can be prepared by blending a maximum of 5% by Volurne of a high molecular weight viscosity index improver with an oil refined by thermal diffusion to increase the viscosity iudex thereof from the range of about to to the range of at least and preferably about to or more. It is also within the scope of the invention to blend with the viscosity index improver a blend of two or more oils that have been refined by thermal diffusion to increase their viscosity indexes.
- the oil composition of the invention therefore, essentially comprises a major amount, preferably at least about 80% by volume, of a thermal diffusion refined oil having a viscosity index of at least 110 and preferably between 115 and about 130 and up to about 5% by volume of a high molecular weight viscosity index improver.
- Compositions within the scope of this definition are characterized by a viscosity index of at least 140, a viscosity of less than 200 SSU at 100 F., a viscosity of at least about 50 SSU at 210 F. and a volatility at atmospheric pressure of less than 5% at about 735 F. and less than 50% at about 800 F.
- High molecular weight viscosity index improvers are Well known in the lubrication art, as exemplified by the discussion thereof in Motor Oils and Engine Lubrication, by Carl W. Georgi, Reinhold Publishing Co. (1950), at pages 196 to 207.
- One is the Paratone viscosity index improver, a butene polymer believed to have the general formula for which the molecular weight is in the range of 10,000 to 15,000.
- Another is Acryloid, a polymer of methacrylic acid ester and higher fatty alcohols generally having a molecular weight Within the range of 5,000 to 20,000.
- Acryloid 763 which has a specific gravity of 0.901, a viscosity of 7200 centistokes at 100 F., and a molecular weight, measured in terms of the centistoke viscosity at 100 F. of a 30% solution of the polymer in toluene, of 350 centistokes.
- a third type is the Santodex viscosity index improver prepared by copolymerization of styrene with olefins having eight to twelve carbon atoms and having the general formula are wherein R stands for an alkyl radical having eight to twelve carbon atoms and the molecular weight is of the same order as for the Paratone and Acryloid types.
- Thermal diffusion as is now well known in the art, is a method that essentially involves applying a tem- 'perature gradient across a thin filmof liquid having dissimilar components, thereby separating the liquid into at least two different fractions, and then physically removing the fractions from one another.
- a tem- 'perature gradient across a thin filmof liquid having dissimilar components, thereby separating the liquid into at least two different fractions, and then physically removing the fractions from one another.
- one of the dissimilar fractions is referred to as the hot wall fraction to indicate that it is the fraction that has accumulated adjacent the hot wall and the other fraction is called the cold wall fraction for similar reasons.
- the degree of separation obtainable by means of thermal diffusion is dependent upon a considerable number of variables including the rate of throughput, the relative rates of withdrawal of the hot and cold wall fractions, the
- the hot wall fractions of oils subjected to thermal diffusion have remarkably increased viscosity index values and are not affected appreciably in so far as volatility is concerned. While the invention is not to be limited by any theory advanced, it is believed that the thermal diffusion process, when applied to hydrocarbon oils, involves a sorting out by molecular types rather than molecular weights and that the hot wall fractions are characterized by an enriched para'flinic content whereas the cold wall fractions tend to have a higher than initial concentration of aromatic constituents.
- thermal diifusion refined as applied to oils and oil blends in this description, is therefore intended to refer to the hot wall fraction obtained by subjecting hydrocarbon oils to thermal diffusion.
- the oil compositions of the invention have a considerable number of important advantages. Prominent among these are their low low-temperature viscosities for promoting easy starting, effective lubrication and reducing engine Wear at low temperatures, high high-temperature viscosity to promote adequate lubrication, minimize engine Wear and reduce friction at operating temperatures, and low volatility to insure adequate oil mileage.
- the oil compositions of the invention are viscosity stable in that they are spared the effects of shear breakdown and consequent permanent reduction in viscosity that is characteristic of the multibranded oils that have heretofore appeared and haveal- "ready lost favor in the market.
- oil compositions of the invention are consider'ed useful primarily as motor lubricating oils, they have many other uses, e.g., as vacuum pump oils, transformer or switch oils, and in many cases where high temperature lubrication is required.
- the cold wall fractions obtained alongwith the'overhead products in the thermal diffusion process also have a variety of uses. They may be used in hydraulic systems and in applica tions requiring oils of high specific gravity.
- Part B.A lubricating oil composition was prepared by blending 61.5% SEN thermal diffusion refined oil (hot wall fraction), and 25.5% 300 SEN thermal diffusion refined oil (hot wall fraction). This blend has a 5% Engler volatility at 739 F. and a 50% Engler volatility at 803 F. To this was added 9% of a heavy oil known as 78 SEE (solvent extracted brightstock) having a viscosity index of 96 and viscosities of 725.8 and 75.0 SSU at 100 F. and 210 F., respectively, and 4% high molecular Weight polymeric viscosity index improver (2% Acryloid 763 and 2% of a Du Pont PL- 164B or LOA-565 as defined heretofore), the percentages being by volume. The viscos'ities and viscosity index of this oil composition are given in Table II.
- Oil composition thus prepared was compared with five commercial triple branded SAE 5W-20 oils identified anonymously herein as oils A, B, C, D and E.
- Oils A, B, C and D are prepared in accordance with the prevailing practice of blending about 8 to 15% by volume of polymeric viscosity index improver with a relatively thin base oil so as to obtain an oil composition of optimum viscosity characteristics at the expense of high volatility and high consumption.
- Oil E is an oil prepared by blending a thicker base oil with about 8 to 15 by volume of polymeric viscosity index improver in order to obtain a less volatile oil composition at the expense of high viscosity at low and starting temperatures.
- the viscosities at 0 F. and 300 F. were obtained by extrapolation from the measured viscosities at 100 and 210 F.
- Oil consumption figures were obtained by subjecting all of the oils in rotation to ordinary driving conditions in a fleet of automobiles and these figures were in effect checked by determinations of the temperatures at which 5 and 50% of the compositions were volatilized and also a determination of the percentage of lubricant remaining after subjecting a 0.15 min. film thereof to a temperature of 300 F. for two hours in a forced draft oven. The higher the residue remaining from this film test, the better the oil is with respect to engine wear and rate of oil consumption. The data from these tests is given in Table II.
- Oils A through D are significantly inferior to the oil composition prepared as described in Parts A and B with reference to oil consumption and volatility.
- the temperatures at which 5 and 50% volatilize are considerably lower than for the oil of the invention.
- the percentages of thin film remaining are appreciably lower, and the consumption in terms of quarts per 1000 miles are substantially higher, than the corresponding figures for the oil composition of the invention.
- a high viscosity index, low viscosity, low volatility, motor oil composition having a viscosity below about 200 SSU at 100 F. and a viscosity of at least SSU at 210 F.; a viscosity index of at least 140; and a volatility at atmospheric pressure of less than 5% at about 735 F.
- said composition consisting essentially of (l) at least by volume of a thermally diffused mineral oil obtained by supjecting a solvent extracted mineral oil having a viscosity index of between and to liquid thermal diffusion under conditions including a temperature gradient, an area over which it is imposed, a spacing between the hot and cold walls, and a flow rate to produce a hot wall fraction having a viscosity index of between and 130, and (2) a maximum of 5% by volume of a high molecular weight polymer viscosity index improver.
- a thermally diffused mineral oil obtained by supjecting a solvent extracted mineral oil having a viscosity index of between and to liquid thermal diffusion under conditions including a temperature gradient, an area over which it is imposed, a spacing between the hot and cold walls, and a flow rate to produce a hot wall fraction having a viscosity index of between and 130, and (2) a maximum of 5% by volume of a high molecular weight polymer viscosity index improver.
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Description
tates This invention relates to oil compositions that are useful primarily as engine lubricating oils and are characterized by a unique and most desirable combination of high viscosity index, low viscosity at low temperatures and low volatility at higher temperatures.
The desirability of providing a lubricating oil having a high viscosity index, i.e., a low viscosity at low temperatures to facilitate cold starting and minimize friction and engine wear while operating at low temperatures and a high viscosity at higher temperatures to insure adequate lubrication and minimize friction and engine wear at engine operating temperatures, has been recognized for some time. The recent trend towards engines of higher horsepower and speed, and toward the use of closer tolerances between moving parts thereof have accentuated the demands for lubricants that will provide effective lubrication under a wide variety of conditions ranging from starting an engine at frigid temperatures to operating it at high speeds for extended periods of time and at average temperatures of several hundred F.
The answer of the oil industry to demands for oils to meet these requirements has been to provide the socalled double and triple branded motor oils. These are generally oils or oil blends containing at least about 8% and as much as 15% by volume of one or more high molecular weight polymers, e.g., polybutenes, well known in the industry as viscosity index improvers. It is possible, for example, to blend enough of a viscosity index improver with an oil having a viscosity index of say 100 to increase its viscosity index to 140 or more and thus make it eligible for classification as a triple branded motor oil such as SAE W-20.
As so often happens, however, this solution to the problem has brought with it several other problems which are of a magnitude suflicient to have resulted in a considerable decline in the popularity of such multi-branded oils. The new problems created by attempts to produce motor oil blends of high viscosity index through the strategy of blending considerable amounts of viscosity index improver with an oil are basically related to the fact that low viscosity at low temperatures goes hand in hand with high volatility at the temperatures to which a motor oil is subjected during engine operation. Blends of thin oil with high proportions of viscosity index improver to raise the viscosity at 210 F. to an acceptable figure were found to have comparatively short useful life in an engine. Investigations showed this to be due to the relatively high volatility at the operating temperature of the engine. Blends of thicker oil with the same amount of viscosity index improver had reduced volatility at the higher temperature and therefore better consumption characteristics, but were too viscous at low starting temperatures. The use of lesser amounts of viscosity improver with thicker oils can result in acceptable values of viscosity at starting temperatures and volatility at engine operating temperatures, but results in a reduction of viscosity at engine operating temperatures to a point that is inadequate for proper lubrication under the conditions of operation.
Thus it becomes apparent that attempts to blend oils and viscosity index improvers to obtain lubricating oils of optimum characteristics have been frustrated by the atent O i 5 2,996,455 Patented Aug. 15, 1961 "ice inescapable fact that at least one of three basic requirements, i.e., low viscosity at starting temperatures, high viscosity at operating temperatures and low volatility at operating temperatures must be sacrificed, or that, in the alternative, an unsatisfactory compromise must be accepted. In addition to this problem, it also developed that the high molecular weight viscosity index improvers tend to undergo shear breakdown under operating conditions when used in high or moderately high concentration. This breakdown is permanent in that the viscosity lost as a result of the breakdown is not regained after the oil has returned to ambient temperature.
The surprising discovery has now been made that an oil composition having all three desirable attributes of low low-temperature viscosity, high high-temperature viscosity (i.e., high viscosity index) and low volatility can be prepared by blending a maximum of 5% by Volurne of a high molecular weight viscosity index improver with an oil refined by thermal diffusion to increase the viscosity iudex thereof from the range of about to to the range of at least and preferably about to or more. It is also within the scope of the invention to blend with the viscosity index improver a blend of two or more oils that have been refined by thermal diffusion to increase their viscosity indexes.
The oil composition of the invention, therefore, essentially comprises a major amount, preferably at least about 80% by volume, of a thermal diffusion refined oil having a viscosity index of at least 110 and preferably between 115 and about 130 and up to about 5% by volume of a high molecular weight viscosity index improver. Compositions within the scope of this definition are characterized by a viscosity index of at least 140, a viscosity of less than 200 SSU at 100 F., a viscosity of at least about 50 SSU at 210 F. and a volatility at atmospheric pressure of less than 5% at about 735 F. and less than 50% at about 800 F.
High molecular weight viscosity index improvers are Well known in the lubrication art, as exemplified by the discussion thereof in Motor Oils and Engine Lubrication, by Carl W. Georgi, Reinhold Publishing Co. (1950), at pages 196 to 207. One is the Paratone viscosity index improver, a butene polymer believed to have the general formula for which the molecular weight is in the range of 10,000 to 15,000. Another is Acryloid, a polymer of methacrylic acid ester and higher fatty alcohols generally having a molecular weight Within the range of 5,000 to 20,000. An example is Acryloid 763 which has a specific gravity of 0.901, a viscosity of 7200 centistokes at 100 F., and a molecular weight, measured in terms of the centistoke viscosity at 100 F. of a 30% solution of the polymer in toluene, of 350 centistokes. A third type is the Santodex viscosity index improver prepared by copolymerization of styrene with olefins having eight to twelve carbon atoms and having the general formula are wherein R stands for an alkyl radical having eight to twelve carbon atoms and the molecular weight is of the same order as for the Paratone and Acryloid types.
' centistokes at 100 F.
Thermal diffusion as is now well known in the art, is a method that essentially involves applying a tem- 'perature gradient across a thin filmof liquid having dissimilar components, thereby separating the liquid into at least two different fractions, and then physically removing the fractions from one another. Inasmuch as this is usually accomplished in apparatus having two closely spaced walls forming a thermal diffusion chamber for confining the liquid while it is subjected to thermal diffusion and one of the walls is relatively heated and the other relatively cooled to impose the tempera- 'ture gradient across the confined liquid, one of the dissimilar fractions is referred to as the hot wall fraction to indicate that it is the fraction that has accumulated adjacent the hot wall and the other fraction is called the cold wall fraction for similar reasons. The degree of separation obtainable by means of thermal diffusion is dependent upon a considerable number of variables including the rate of throughput, the relative rates of withdrawal of the hot and cold wall fractions, the
magnitude of the temperature gradient imposed, the spacing between the hot and cold Wall surfaces, the area of said surfaces, and the like. y
In the method of the invention, it has been found that the hot wall fractions of oils subjected to thermal diffusion have remarkably increased viscosity index values and are not affected appreciably in so far as volatility is concerned. While the invention is not to be limited by any theory advanced, it is believed that the thermal diffusion process, when applied to hydrocarbon oils, involves a sorting out by molecular types rather than molecular weights and that the hot wall fractions are characterized by an enriched para'flinic content whereas the cold wall fractions tend to have a higher than initial concentration of aromatic constituents. The term thermal diifusion refined, as applied to oils and oil blends in this description, is therefore intended to refer to the hot wall fraction obtained by subjecting hydrocarbon oils to thermal diffusion.
The oil compositions of the invention have a considerable number of important advantages. Prominent among these are their low low-temperature viscosities for promoting easy starting, effective lubrication and reducing engine Wear at low temperatures, high high-temperature viscosity to promote adequate lubrication, minimize engine Wear and reduce friction at operating temperatures, and low volatility to insure adequate oil mileage. In addition, the oil compositions of the invention are viscosity stable in that they are spared the effects of shear breakdown and consequent permanent reduction in viscosity that is characteristic of the multibranded oils that have heretofore appeared and haveal- "ready lost favor in the market.
While the oil compositions of the invention are consider'ed useful primarily as motor lubricating oils, they have many other uses, e.g., as vacuum pump oils, transformer or switch oils, and in many cases where high temperature lubrication is required. The cold wall fractions obtained alongwith the'overhead products in the thermal diffusion process also have a variety of uses. They may be used in hydraulic systems and in applica tions requiring oils of high specific gravity.
The advantages and utility of the composition and method of the invention will become further apparent from the detailed description in the following example.
4 EXAMPLE Part A.Solvent extracted neutral oils having viscosities of 140 and 300 at F., and therefore identified as 140 SEN and 300 SEN oils, respectively, were refined by thermal diffusion in a six foot vertical, center feed concentric tube column wherein the thermal dififusion separation chamber was formed by the outer wall of the inner tube and the inner wall of the outer tube, the opposed surfaces of the chamber-forming walls being spaced apart a distance of 0.03". The hot wall was maintained at a temperature of 445 and the cold wall was maintained at F. The oils were introduced into the thermal diffusion columns at rates of approximately 35 nil/hr. and the rates of withdrawal of the hot wall fraction from the top and the cold wall fraction from the bottom were maintained approximately equal. The initial and final viscosities and viscosity indexes, and the 5 and 50% Engler distillation values, of the thermal diffused oils withdrawn from the top of the column are tabulated in Table I immediately below:
Part B.A lubricating oil composition was prepared by blending 61.5% SEN thermal diffusion refined oil (hot wall fraction), and 25.5% 300 SEN thermal diffusion refined oil (hot wall fraction). This blend has a 5% Engler volatility at 739 F. and a 50% Engler volatility at 803 F. To this was added 9% of a heavy oil known as 78 SEE (solvent extracted brightstock) having a viscosity index of 96 and viscosities of 725.8 and 75.0 SSU at 100 F. and 210 F., respectively, and 4% high molecular Weight polymeric viscosity index improver (2% Acryloid 763 and 2% of a Du Pont PL- 164B or LOA-565 as defined heretofore), the percentages being by volume. The viscos'ities and viscosity index of this oil composition are given in Table II.
Part C.-The oil composition thus prepared was compared with five commercial triple branded SAE 5W-20 oils identified anonymously herein as oils A, B, C, D and E. Oils A, B, C and D are prepared in accordance with the prevailing practice of blending about 8 to 15% by volume of polymeric viscosity index improver with a relatively thin base oil so as to obtain an oil composition of optimum viscosity characteristics at the expense of high volatility and high consumption. Oil E is an oil prepared by blending a thicker base oil with about 8 to 15 by volume of polymeric viscosity index improver in order to obtain a less volatile oil composition at the expense of high viscosity at low and starting temperatures.
In order to properly compare the five commercial oils with the oil of the example prepared in accordance with the invention, the viscosities at 0 F. and 300 F. were obtained by extrapolation from the measured viscosities at 100 and 210 F. Oil consumption figures were obtained by subjecting all of the oils in rotation to ordinary driving conditions in a fleet of automobiles and these figures were in effect checked by determinations of the temperatures at which 5 and 50% of the compositions were volatilized and also a determination of the percentage of lubricant remaining after subjecting a 0.15 min. film thereof to a temperature of 300 F. for two hours in a forced draft oven. The higher the residue remaining from this film test, the better the oil is with respect to engine wear and rate of oil consumption. The data from these tests is given in Table II.
Table II Oil Oomposition OilA OilB OilC OilD OilE of Parts AandB V.I 148.8 150.1 155.4 153.5 152.1 121.1 Measured Viscosity,
SSU:
100]? 194.7 166.8 160.8 167.3 150.8 224.7 210]? 52.56 49.11 49.4 50.11 47. 46 50.37 Extrapolated Viscos- 'y,SSU:
F 4,300 3,900 3,200 3,300 3,100 10,800 300]? 38.8 37.3 37.6 38.1 36.9 37.2 Engler Volatility:
F-- 739 675 665 647 680 728 50% F 808 775 745 762 775 793 Thin Film Evaporation, Percent Lubricant Remaining--." 72 56.8 38.2 34.6 62.1 75.3 Average Oil Consumption, qts./1,000 miles 1.03 1.55 1.49 1.41 1.54 1.05
The data in this table shows that the viscosity, consumption and volatility characteristics of the oil of the invention could not be duplicated in any one of the five competitive oils tested. The volatility of the thermal difiusion refined oils before addition of the viscosity index improver is substantially the same as indicated for the final blend.
Oils A through D are significantly inferior to the oil composition prepared as described in Parts A and B with reference to oil consumption and volatility. The temperatures at which 5 and 50% volatilize are considerably lower than for the oil of the invention. The percentages of thin film remaining are appreciably lower, and the consumption in terms of quarts per 1000 miles are substantially higher, than the corresponding figures for the oil composition of the invention.
Comparison of the oil of the invention with oil E, on the other hand, shows that while the volatility and characterstics of the oils are approximately equal, the viscosity index is considerably lower. The high viscosities of oil E at 100 F., and particularly at 0 F., indicate poor cold weather starting characteristics.
Only the oil prepared in accordance with the invention has the hitherto elusive and desirable combination of high viscosity index, low low-temperature viscosity, low volatility and minimal loss of viscosity resulting from shear breakdown.
It is to be understood that numerous modifications will readily become apparent to those skilled in the art upon reading this description. All such modifications are intended to be included within the scope of the invention as defined in the appended claim.
We claim:
A high viscosity index, low viscosity, low volatility, motor oil composition having a viscosity below about 200 SSU at 100 F. and a viscosity of at least SSU at 210 F.; a viscosity index of at least 140; and a volatility at atmospheric pressure of less than 5% at about 735 F. and less than 50% at 800 F., said composition consisting essentially of (l) at least by volume of a thermally diffused mineral oil obtained by supjecting a solvent extracted mineral oil having a viscosity index of between and to liquid thermal diffusion under conditions including a temperature gradient, an area over which it is imposed, a spacing between the hot and cold walls, and a flow rate to produce a hot wall fraction having a viscosity index of between and 130, and (2) a maximum of 5% by volume of a high molecular weight polymer viscosity index improver.
References Cited in the file of this patent UNITED STATES PATENTS 2,489,281 Foehr Nov. 29, 1949 2,492,789 Evans et al Dec. 27, 1949 2,541,070 Jones et al. Feb. 13, 1951 2,541,071 Jones et al. Feb. 13, 1951 2,694,685 Bartlett Nov. 16, 1954 2,756,197 Thorpe et al. July 24, 1956 OTHER REFERENCES Georgi: Motor Oil and Engine Lubrication, pub. by Reinhold Pub. Corp., N.Y., 1950, pages and 151.
Kalichevsky: Modern Methods of Refining Lubricating Oils, pub. by Reinhold Pub. Corp., N.Y., 1938, p. 20.
Chemical Refining of Petroleum, Kalichevsky et al.,
45 Reinhold Pub. Corp., N.Y., 1942, 2nd ed., page 413.
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US631064A US2996455A (en) | 1956-12-28 | 1956-12-28 | High viscosity index, low viscosity, low volatility motor oil |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3251772A (en) * | 1962-01-30 | 1966-05-17 | Kaspar Winkler & Co | Lubricating composition containing cross-linked polymer |
US3271121A (en) * | 1963-03-14 | 1966-09-06 | Sinclair Research Inc | Ethylene-styrene copolymer as pour point depressant |
DE2210430A1 (en) * | 1971-03-05 | 1973-01-25 | Shell Int Research | VISCOSITY INDEX IMPROVED LUBRICATING OIL AND ITS MANUFACTURING |
US3903003A (en) * | 1974-03-06 | 1975-09-02 | Shell Oil Co | Lubricating compositions containing an amido-amine reaction product of a terminally carboxylated isoprene polymer |
US3977979A (en) * | 1973-09-14 | 1976-08-31 | George A. Goulston Company, Inc. | Yarn finish formulations |
US4031020A (en) * | 1974-05-31 | 1977-06-21 | Nippon Oil Company, Ltd. | Central system fluid composition |
US4081390A (en) * | 1975-05-22 | 1978-03-28 | Orobis Limited | Viscosity index improver composition |
US4853337A (en) * | 1987-05-11 | 1989-08-01 | Exxon Chemicals Patents Inc. | Blending of hydrocarbon liquids |
US4897176A (en) * | 1986-06-20 | 1990-01-30 | Exxon Chemical Patents Inc. | Method of preparing baseoil blend of predetermined coking tendency |
US5049257A (en) * | 1987-07-17 | 1991-09-17 | Sodick Co., Ltd. | Fluid for electrical discharge machining |
US5763374A (en) * | 1994-08-10 | 1998-06-09 | Sanyo Chemical Industries, Ltd. | Lubricating oil compositions of reduced high-temperature high-shear viscosity |
US9359565B2 (en) | 2013-01-16 | 2016-06-07 | Exxonmobil Research And Engineering Company | Field enhanced separation of hydrocarbon fractions |
US9498738B2 (en) | 2014-07-18 | 2016-11-22 | Exxonmobil Research And Engineering Company | Field enhanced separation apparatus |
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US2489281A (en) * | 1947-04-04 | 1949-11-29 | California Research Corp | Methacrylates in constant viscosity oils |
US2492789A (en) * | 1946-11-21 | 1949-12-27 | Jasco Inc | Lubricating oil composition |
US2541071A (en) * | 1947-07-22 | 1951-02-13 | Standard Oil Co | Continuous method for separating materials by liquid thermal diffusion |
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US2694685A (en) * | 1947-02-14 | 1954-11-16 | Standard Oil Dev Co | Maleinoid-vinyl copolymer and its use in lubricants |
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US2492789A (en) * | 1946-11-21 | 1949-12-27 | Jasco Inc | Lubricating oil composition |
US2694685A (en) * | 1947-02-14 | 1954-11-16 | Standard Oil Dev Co | Maleinoid-vinyl copolymer and its use in lubricants |
US2489281A (en) * | 1947-04-04 | 1949-11-29 | California Research Corp | Methacrylates in constant viscosity oils |
US2541070A (en) * | 1947-07-11 | 1951-02-13 | Standard Oil Co | Method of separating dissimilar components in petroleum products by liquid thermal diffusion |
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Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
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US3251772A (en) * | 1962-01-30 | 1966-05-17 | Kaspar Winkler & Co | Lubricating composition containing cross-linked polymer |
US3271121A (en) * | 1963-03-14 | 1966-09-06 | Sinclair Research Inc | Ethylene-styrene copolymer as pour point depressant |
DE2210430A1 (en) * | 1971-03-05 | 1973-01-25 | Shell Int Research | VISCOSITY INDEX IMPROVED LUBRICATING OIL AND ITS MANUFACTURING |
US3977979A (en) * | 1973-09-14 | 1976-08-31 | George A. Goulston Company, Inc. | Yarn finish formulations |
US3903003A (en) * | 1974-03-06 | 1975-09-02 | Shell Oil Co | Lubricating compositions containing an amido-amine reaction product of a terminally carboxylated isoprene polymer |
US4031020A (en) * | 1974-05-31 | 1977-06-21 | Nippon Oil Company, Ltd. | Central system fluid composition |
US4081390A (en) * | 1975-05-22 | 1978-03-28 | Orobis Limited | Viscosity index improver composition |
US4897176A (en) * | 1986-06-20 | 1990-01-30 | Exxon Chemical Patents Inc. | Method of preparing baseoil blend of predetermined coking tendency |
US4853337A (en) * | 1987-05-11 | 1989-08-01 | Exxon Chemicals Patents Inc. | Blending of hydrocarbon liquids |
US5049257A (en) * | 1987-07-17 | 1991-09-17 | Sodick Co., Ltd. | Fluid for electrical discharge machining |
US5763374A (en) * | 1994-08-10 | 1998-06-09 | Sanyo Chemical Industries, Ltd. | Lubricating oil compositions of reduced high-temperature high-shear viscosity |
US9359565B2 (en) | 2013-01-16 | 2016-06-07 | Exxonmobil Research And Engineering Company | Field enhanced separation of hydrocarbon fractions |
US9498738B2 (en) | 2014-07-18 | 2016-11-22 | Exxonmobil Research And Engineering Company | Field enhanced separation apparatus |
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