EP0482693A1 - Lubricant compositions for autotraction - Google Patents
Lubricant compositions for autotraction Download PDFInfo
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- EP0482693A1 EP0482693A1 EP91202610A EP91202610A EP0482693A1 EP 0482693 A1 EP0482693 A1 EP 0482693A1 EP 91202610 A EP91202610 A EP 91202610A EP 91202610 A EP91202610 A EP 91202610A EP 0482693 A1 EP0482693 A1 EP 0482693A1
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M111/00—Lubrication compositions characterised by the base-material being a mixture of two or more compounds covered by more than one of the main groups C10M101/00 - C10M109/00, each of these compounds being essential
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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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/08—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing oxygen
- C10M105/32—Esters
- C10M105/48—Esters of carbonic acid
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- 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
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum 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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
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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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/68—Esters
- C10M129/84—Esters of carbonic acid
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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
- C10M143/00—Lubricating compositions characterised by the additive being a macromolecular hydrocarbon or such hydrocarbon modified by oxidation
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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
- C10M145/00—Lubricating compositions characterised by the additive being a macromolecular compound containing oxygen
- C10M145/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M145/10—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
- C10M145/12—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 monocarboxylic
- C10M145/14—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
- 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
- C10M169/041—Mixtures of base-materials and additives the additives being macromolecular compounds only
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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
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2203/1025—Aliphatic fractions used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- C10M2203/104—Aromatic fractions
- C10M2203/1045—Aromatic fractions used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
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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
- C10M2203/108—Residual fractions, e.g. bright stocks
- C10M2203/1085—Residual fractions, e.g. bright stocks used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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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
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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
- C10M2205/0206—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/32—Esters of carbonic acid
- C10M2207/325—Esters of carbonic acid used as base material
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
Definitions
- This invention relates to an improved lubricant composition for use in internal combustion engines.
- synthetic bases are able to eliminate or at least alleviate the drawbacks often encountered when using only mineral bases, these requiring 1) the presence of extremely fluid fractions to obtain the desired viscosity at low temperature and to limit volatility, 2) the presence of a high percentage of viscosity index improvers to improve the initial VI, and 3) other additives for satisfying all the other lubricant performance requirements.
- lubricant compositions For use in internal combustion engines, lubricant compositions must possess certain characteristics, namely thermal stability, oxidation resistance, low volatility and such viscosity-temperature characteristics as to allow both cold starting and good lubrication at maximum operating temperature.
- Lubricant compositions which have been proposed for this purpose include those containing higher dialkyl carbonates in combination with a mineral oil and usual additives. These compositions, which are described for example in U.S. 2,387,999. U.S. 2,758,975, U.S. 3,642,858 and European patent application 89,709, result in various improvements compared with compositions based on carboxylic esters, in particular in relation to increased thermal, hydrolytic and oxidative stability.
- a lubricant composition comprising:
- component a) is present in a quantity of between 0 and 60% by weight, component b) from 20 to 60% by weight, component c) from 15 to 30% by weight, component d) from 8 to 10% by weight and component e) from 5 to 10% by weight.
- Lubricant oils which can be used as component a) of the composition of the present invention are oils of mineral origin obtained by petroleum distillation followed by solvent and/or hydrogen refining generally having a viscosity index of 102-108, a pour point of between -12 ° C and -6 ° C and a Noack evaporation loss of 12-42%.
- Synthetic base oils which can be used as component b) of the composition of the present invention are oils of synthetic origin and can be obtained by the polymerization of terminal or internal olefins followed by purification, or by isomerization and/or alkylation of petroleum fractions followed by purification.
- Alcohols which can be used for preparing component c) of the composition of the present invention are mixtures containing at least 98% and preferably at least 99% of aliphatic alcohols with a linear or essentially linear hydrocarbon chain carrying a -CH 2 -OH group on a non-terminal carbon atom, the total number of carbon atoms in the alcohol varying from 10 to 18 and preferably from 13 to 16. More specifically, alcohols suitable for the purpose are alcohols definable by the formula: where m is a whole number and n is zero or a whole number, with the condition that the total number of carbon atoms in the molecule is between 10 and 18 and preferably between 13 and 16.
- Preferred mixtures are those in which the -CH 2 -OH group is prevalently in position 2 of the chain.
- Alcohols (I) suitable for the purpose include the branched fraction of the oxo-alcohols obtained by hydroformylation, using carbon monoxide and hydrogen, of linear or essentially linear olefins with a statistical internal or terminal double bond, operating with cobalt or rhodium catalysts.
- This branched oxo-alcohol fraction can be separated from the linear fraction by fractional crystallization operating in the presence of a hydrocarbon or ether solvent, as described for example in U.S. patent 4,670,606.
- a mixture of linear and branched chain oxo-alcohols is dissolved in a liquid hydrocarbon solvent containing from 3 to 5 carbon atoms in the molecule, or in methyl tert-butyl ether.
- the solution is cooled to a temperature within the range of -20 ° C to -52 ° C to cause separation of a solid phase consisting of the linear oxo-alcohols, and a liquid phase consisting of a solution of the branched oxo-alcohols in the chosen solvent.
- the branched oxo-alcohols can generally be separated form this solution with a purity of the order of 95%, and be purified by further crystallization to obtain the mixture of alcohols (I) suitable for the purposes of the present invention, with a purity exceeding 98% and preferably exceeding 99%.
- Such a mixture of alcohols (I) is then transesterified with a lower dialkyl carbonate to give component b) of the composition of the present invention.
- This reaction can be effected by bringing the reagents into contact in the presence of a basic catalyst operating at high temperature and under reduced pressure, and eliminating the lower aliphatic alcohol evolved as the reaction by-product, as is well known in the art and described in the examples given in European patent application publication No. 89,709.
- Preferred lower dialkyl carbonates are dimethyl carbonate and diethyl carbonate.
- Active transesterification catalysts useful for the purpose are sodium methylate and sodium ethylate.
- component b) of the composition of the present invention On termination of the transesterification reaction the long-chain dialkyl carbonate is recovered to constitute component b) of the composition of the present invention, its characteristics falling generally within the following value ranges (general and preferred):
- Such a dialkyl carbonate also has desirable characteristics in relation to low temperature rheology values, oxidation stability, elastomer compatibility, biodegradability and toxicity.
- Component d) of the composition of the present invention consists of a parcel of additives usually used in lubricants and specifically dispersants, antiwear and antirust additives, metal passivators and copper deactivators, detergent additives (superbasic and neutral) and antioxidants. These additives are usually chosen from the following classes of compounds:
- Component e) of the composition of the present invention consists of a collection of additives able to raise the viscosity index and lower the pour point of the resultant lubricant composition.
- additives are usually chosen from the following classes of compounds: olefinic copolymers, methacrylic copolymers, olefinic/methacrylic copolymers. Said additives can also have other properties such as antioxidant, dispersant and antiwear, together with the basic properties of viscosity index and pour point improvers.
- Typical lubricant compositions suitable for four-stroke gasoline and diesel engines contain the aforesaid components in the following weight percentages:
- the long-chain dialkyl carbonate used as component c) in the lubricant compositions enables lubricant compositions for autotraction to be formulated possessing unexpectedly good overall rheological and engine performance characteristics.
- the particular dialkyl carbonate structure enables a high viscosity index, a low pour point and a low volatility to be obtained simultaneously.
- the high polarity of the carbonate group together with its structural characteristics enables high engine performance to be obtained together with a reduction in the level of addition of component d).
- the high polarity results in good dispersing action towards engine sludge (enabling dispersants to be reduced by about 30% in the lubricant composition), the greasing of metal surfaces subject to wear (enabling antiwear additives to be reduced by about 20% in the lubricant composition), and an antirust and electrochemical protection action on ferrous and non-ferrous metal surfaces (enabling antirust additives, metal passivators and copper deactivators to be reduced by about 30%).
- the high thermal and oxidative stability of component c) enables the antioxidant additives to be reduced by about 30% in the lubricant composition, and the absence of acid compounds deriving from decomposition phenomena enables the superbasic detergent additives to be reduced by about 20%.
- component c) of the composition is practically inert towards the elastomers usually present in the lubrication circuit.
- lubricant compositions can be formulated with a medium-high nitrogen content, avoiding the addition of specific additives normally introduced to overcome the elastomer compatibility tests scheduled in the most severe specifications such as CCMC and VW specifications.
- oxo-alcohols are described as alcohols suitable for preparing long-chain dialkyl carbonates for lubricant compositions, however without separation of the linear fraction from the branched fraction.
- the use of the mixture of alcohols (I) with the aforesaid characteristics is critical in order to obtain the required characteristics for the dialkyl carbonates and for the lubricant compositions which incorporate them, as will be apparent from the experimental examples which are given hereinafter to better illustrate the present invention.
- This oxo-alcohol mixture is the product of the hydroformylation of substantially linear olefins with carbon monoxide and hydrogen in the presence of a catalyst.
- the mixture is subjected to fractional crystallization at low temperature in the presence of a hydrocarbon solvent as described in U.S. patent 4,670,606, to separate a solid linear alcohol fraction from a liquid fraction containing 95% by weight of branched alcohols.
- This liquid fraction is purified by a second fractional crystallization similar to the first, to separate a liquid fraction with a branched alcohol content exceeding 99% by weight.
- the mixture of branched alcohols (I) obtained in Example 1 is transesterified with dimethyl carbonate operating with sodium ethylate as catalyst, as described in European patent application No. 89,709, to obtain a dialkyl carbonate (I) with an average molecular weight of 470 and having the following characteristics:
- the linear and branched oxo-alcohol mixture obtained in the hydroformylation reaction is transesterified (without previous separation) with dimethyl carbonate using sodium ethylate as catalyst in accordance with Example 2, to obtain a dialkyl carbonate (II) with an average molecular weight of 470, a viscosity index of 130, a pour point of + 12 ° C and a Noack volatility of 15%.
- the lubricant composition (A) of the present invention and the comparison lubricant composition (B) are prepared in accordance with the following Table I.
- compositions (A) and (B) are subjected to a series of rheological and laboratory tests aimed at evaluating the extent to which they satisfy the requirements of the European Sequence scheduled by constructors for CCMC oil classification and the requirements of the American sequence scheduled by constructors for API oil classification.
- the results are given in the following Table II.
- the lubricant composition (A) in accordance with the present invention satisfies all the requirements of the American API and European CCMC Sequences.
- the comparison lubricant composition (B) does not satisfy the requirements of viscosity at -25 ° C, BPT, stable pour point or Noack volatility. This behaviour is related to the different physico-chemical characteristics of the dialkyl carbonates (I) and (II) used in the compositions.
- both the lubricant compositions satisfy all tests by a wide margin on the set limits.
- dialkyl carbonates (I) of the present invention are lubricant compositions obtained which have optimum performance characteristics from both the engine and rheological aspects.
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Abstract
Description
- This invention relates to an improved lubricant composition for use in internal combustion engines.
- It is known in the art to use synthetic bases in formulating lubricant compositions both of single grade and of multigrade type. In this respect, synthetic bases are able to eliminate or at least alleviate the drawbacks often encountered when using only mineral bases, these requiring 1) the presence of extremely fluid fractions to obtain the desired viscosity at low temperature and to limit volatility, 2) the presence of a high percentage of viscosity index improvers to improve the initial VI, and 3) other additives for satisfying all the other lubricant performance requirements.
- For use in internal combustion engines, lubricant compositions must possess certain characteristics, namely thermal stability, oxidation resistance, low volatility and such viscosity-temperature characteristics as to allow both cold starting and good lubrication at maximum operating temperature.
- Lubricant compositions which have been proposed for this purpose include those containing higher dialkyl carbonates in combination with a mineral oil and usual additives. These compositions, which are described for example in U.S. 2,387,999. U.S. 2,758,975, U.S. 3,642,858 and European patent application 89,709, result in various improvements compared with compositions based on carboxylic esters, in particular in relation to increased thermal, hydrolytic and oxidative stability.
- A particular class of higher alkyl carbonates has now been found which results in a general rheological and engine performance improvement in the lubricant compositions in which they are incorporated, and thus make them desirable for use as high-performance lubricant compositions for four-stroke gasoline and diesel engines.
- In accordance therewith the present invention provides a lubricant composition comprising:
- a) from 0 to 90% by weight of a mineral base oil;
- b) from 0 to 90% by weight of a synthetic base oil;
- c) from 5 to 50% by weight of a long-chain dialkyl carbonate;
- d) from 6 to 12% by weight of a parcel of usual additives; and
- e) from 0 to 15% by weight of viscosity index and pour point improvement additives;
- In the preferred embodiment, component a) is present in a quantity of between 0 and 60% by weight, component b) from 20 to 60% by weight, component c) from 15 to 30% by weight, component d) from 8 to 10% by weight and component e) from 5 to 10% by weight.
- Lubricant oils which can be used as component a) of the composition of the present invention are oils of mineral origin obtained by petroleum distillation followed by solvent and/or hydrogen refining generally having a viscosity index of 102-108, a pour point of between -12 ° C and -6 ° C and a Noack evaporation loss of 12-42%.
- Synthetic base oils which can be used as component b) of the composition of the present invention are oils of synthetic origin and can be obtained by the polymerization of terminal or internal olefins followed by purification, or by isomerization and/or alkylation of petroleum fractions followed by purification.
- Alcohols which can be used for preparing component c) of the composition of the present invention are mixtures containing at least 98% and preferably at least 99% of aliphatic alcohols with a linear or essentially linear hydrocarbon chain carrying a -CH2-OH group on a non-terminal carbon atom, the total number of carbon atoms in the alcohol varying from 10 to 18 and preferably from 13 to 16. More specifically, alcohols suitable for the purpose are alcohols definable by the formula:
where m is a whole number and n is zero or a whole number, with the condition that the total number of carbon atoms in the molecule is between 10 and 18 and preferably between 13 and 16. - Preferred mixtures are those in which the -CH2-OH group is prevalently in position 2 of the chain.
- Mixtures of alcohols (I) suitable for the purpose include the branched fraction of the oxo-alcohols obtained by hydroformylation, using carbon monoxide and hydrogen, of linear or essentially linear olefins with a statistical internal or terminal double bond, operating with cobalt or rhodium catalysts. This branched oxo-alcohol fraction can be separated from the linear fraction by fractional crystallization operating in the presence of a hydrocarbon or ether solvent, as described for example in U.S. patent 4,670,606. According to this patent, a mixture of linear and branched chain oxo-alcohols is dissolved in a liquid hydrocarbon solvent containing from 3 to 5 carbon atoms in the molecule, or in methyl tert-butyl ether. The solution is cooled to a temperature within the range of -20 ° C to -52 ° C to cause separation of a solid phase consisting of the linear oxo-alcohols, and a liquid phase consisting of a solution of the branched oxo-alcohols in the chosen solvent. The branched oxo-alcohols can generally be separated form this solution with a purity of the order of 95%, and be purified by further crystallization to obtain the mixture of alcohols (I) suitable for the purposes of the present invention, with a purity exceeding 98% and preferably exceeding 99%.
- Such a mixture of alcohols (I) is then transesterified with a lower dialkyl carbonate to give component b) of the composition of the present invention. This reaction can be effected by bringing the reagents into contact in the presence of a basic catalyst operating at high temperature and under reduced pressure, and eliminating the lower aliphatic alcohol evolved as the reaction by-product, as is well known in the art and described in the examples given in European patent application publication No. 89,709. Preferred lower dialkyl carbonates are dimethyl carbonate and diethyl carbonate. Active transesterification catalysts useful for the purpose are sodium methylate and sodium ethylate.
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- Such a dialkyl carbonate also has desirable characteristics in relation to low temperature rheology values, oxidation stability, elastomer compatibility, biodegradability and toxicity.
- Component d) of the composition of the present invention consists of a parcel of additives usually used in lubricants and specifically dispersants, antiwear and antirust additives, metal passivators and copper deactivators, detergent additives (superbasic and neutral) and antioxidants. These additives are usually chosen from the following classes of compounds:
- alkyl/alkenyl succinimides, succinic esters; alkyl/aryl dithiophosphates of zinc and olefins; ethoxylates, esters and hemiesters of substituted succinic acids; unsaturated or carbonyl compounds of chelating action; heterocyclic compounds; metal salts (neutral and superbasic) of alkyl and aryl sulphonic acids, salicylic acids, phenols and substituted phenols; sterically hindered amines and phenols; sulphurated compounds.
- Component e) of the composition of the present invention consists of a collection of additives able to raise the viscosity index and lower the pour point of the resultant lubricant composition.
- These additives are usually chosen from the following classes of compounds: olefinic copolymers, methacrylic copolymers, olefinic/methacrylic copolymers. Said additives can also have other properties such as antioxidant, dispersant and antiwear, together with the basic properties of viscosity index and pour point improvers.
-
- The long-chain dialkyl carbonate used as component c) in the lubricant compositions enables lubricant compositions for autotraction to be formulated possessing unexpectedly good overall rheological and engine performance characteristics. In this respect, the particular dialkyl carbonate structure enables a high viscosity index, a low pour point and a low volatility to be obtained simultaneously. In addition the high polarity of the carbonate group together with its structural characteristics enables high engine performance to be obtained together with a reduction in the level of addition of component d). In particular the high polarity results in good dispersing action towards engine sludge (enabling dispersants to be reduced by about 30% in the lubricant composition), the greasing of metal surfaces subject to wear (enabling antiwear additives to be reduced by about 20% in the lubricant composition), and an antirust and electrochemical protection action on ferrous and non-ferrous metal surfaces (enabling antirust additives, metal passivators and copper deactivators to be reduced by about 30%). The high thermal and oxidative stability of component c) enables the antioxidant additives to be reduced by about 30% in the lubricant composition, and the absence of acid compounds deriving from decomposition phenomena enables the superbasic detergent additives to be reduced by about 20%. Finally, component c) of the composition is practically inert towards the elastomers usually present in the lubrication circuit. As a result, lubricant compositions can be formulated with a medium-high nitrogen content, avoiding the addition of specific additives normally introduced to overcome the elastomer compatibility tests scheduled in the most severe specifications such as CCMC and VW specifications.
- It should be noted that in the known art oxo-alcohols are described as alcohols suitable for preparing long-chain dialkyl carbonates for lubricant compositions, however without separation of the linear fraction from the branched fraction. According to the present invention the use of the mixture of alcohols (I) with the aforesaid characteristics is critical in order to obtain the required characteristics for the dialkyl carbonates and for the lubricant compositions which incorporate them, as will be apparent from the experimental examples which are given hereinafter to better illustrate the present invention.
-
- This oxo-alcohol mixture is the product of the hydroformylation of substantially linear olefins with carbon monoxide and hydrogen in the presence of a catalyst.
- The mixture is subjected to fractional crystallization at low temperature in the presence of a hydrocarbon solvent as described in U.S. patent 4,670,606, to separate a solid linear alcohol fraction from a liquid fraction containing 95% by weight of branched alcohols. This liquid fraction is purified by a second fractional crystallization similar to the first, to separate a liquid fraction with a branched alcohol content exceeding 99% by weight.
-
- The mixture of branched alcohols (I) obtained in Example 1 is transesterified with dimethyl carbonate operating with sodium ethylate as catalyst, as described in European patent application No. 89,709, to obtain a dialkyl carbonate (I) with an average molecular weight of 470 and having the following characteristics:
- For comparison purposes the linear and branched oxo-alcohol mixture obtained in the hydroformylation reaction is transesterified (without previous separation) with dimethyl carbonate using sodium ethylate as catalyst in accordance with Example 2, to obtain a dialkyl carbonate (II) with an average molecular weight of 470, a viscosity index of 130, a pour point of + 12 ° C and a Noack volatility of 15%.
-
- The compositions (A) and (B) are subjected to a series of rheological and laboratory tests aimed at evaluating the extent to which they satisfy the requirements of the European Sequence scheduled by constructors for CCMC oil classification and the requirements of the American sequence scheduled by constructors for API oil classification. The results are given in the following Table II.
- From the aforegoing data it can be seen that the lubricant composition (A) in accordance with the present invention satisfies all the requirements of the American API and European CCMC Sequences. In contrast, the comparison lubricant composition (B) does not satisfy the requirements of viscosity at -25 ° C, BPT, stable pour point or Noack volatility. This behaviour is related to the different physico-chemical characteristics of the dialkyl carbonates (I) and (II) used in the compositions.
- With regard to the engine tests scheduled by the same American API and European CCMC sequences, both the lubricant compositions satisfy all tests by a wide margin on the set limits. However only by using the dialkyl carbonates (I) of the present invention are lubricant compositions obtained which have optimum performance characteristics from both the engine and rheological aspects.
said composition being characterised in that the component c) is the product of transesterification of a lower dialkyl carbonate with an alcoholic mixture consisting of at least 98% by weight of aliphatic alcohols with a linear or essentially linear hydrocarbon chain carrying a -CH2-OH group on a non-terminal carbon atom, the total number of carbon atoms in the alcohol varying from 10 to 18 and preferably from 13 to 16.
Claims (10)
said composition being characterised in that the component c) is the product of transesterification of a lower dialkyl carbonate with an alcoholic mixture consisting of at least 98% by weight of aliphatic alcohols with a linear or essentially linear hydrocarbon chain carrying a -CH2-OH group on a non-terminal carbon atom, the total number of carbon atoms in the alcohol varying from 10 to 18.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT02181290A IT1243858B (en) | 1990-10-19 | 1990-10-19 | LUBRICANT COMPOSITIONS FOR AUTOTRATION. |
IT2181290 | 1990-10-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0482693A1 true EP0482693A1 (en) | 1992-04-29 |
EP0482693B1 EP0482693B1 (en) | 1994-01-19 |
Family
ID=11187197
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP91202610A Expired - Lifetime EP0482693B1 (en) | 1990-10-19 | 1991-10-07 | Lubricant compositions for autotraction |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0482693B1 (en) |
JP (1) | JP3069872B2 (en) |
KR (1) | KR940008391B1 (en) |
CN (1) | CN1029006C (en) |
AT (1) | ATE100488T1 (en) |
AU (1) | AU640823B2 (en) |
BR (1) | BR9104532A (en) |
CA (1) | CA2053691C (en) |
DE (1) | DE69101047T2 (en) |
DK (1) | DK0482693T3 (en) |
EC (1) | ECSP910786A (en) |
ES (1) | ES2048555T3 (en) |
HU (1) | HU213625B (en) |
IT (1) | IT1243858B (en) |
MX (1) | MX173927B (en) |
PL (1) | PL167993B1 (en) |
PT (1) | PT99284B (en) |
RU (1) | RU2012591C1 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562851A (en) * | 1994-12-21 | 1996-10-08 | Exxon Chemical Patents Inc. | Sulfur-containing carbonate reaction products as lubricating oil antiwear additives |
EP0987312A1 (en) * | 1998-08-22 | 2000-03-22 | Minebea Co., Ltd. | Bearing grease composition |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1270956B (en) * | 1993-07-29 | 1997-05-26 | Euron Spa | LOW SMOKE LUBRICANT COMPOSITION FOR TWO STROKE ENGINES |
IT1282788B1 (en) * | 1996-06-04 | 1998-03-31 | Euron Spa | LUBRICANT COMPOSITIONS WITH LOW PARTICULATE EMISSIONS FOR INTERNAL COMBUSTION ENGINES |
CN113234054A (en) * | 2014-02-13 | 2021-08-10 | 亨斯迈石油化学有限责任公司 | Dialkyl carbonates, methods of making and using the same |
CN103992827B (en) * | 2014-05-20 | 2016-05-18 | 美孚美斯克(泉州)化工有限公司 | A kind of lubricated antiwear and energy-saving increases the composite additive for gasoline of power |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758975A (en) * | 1952-07-02 | 1956-08-14 | Exxon Research Engineering Co | Synthetic lubricants |
EP0089709A1 (en) * | 1982-03-19 | 1983-09-28 | AGIP PETROLI S.p.A. | Synthesis of higher alcohol carbonates and their use as synthetic lubricants |
EP0154363A1 (en) * | 1984-02-24 | 1985-09-11 | ENICHEM AUGUSTA S.p.A. | Process for separating linear-chain oxo-alcohols from mixtures of linear and branched-chain oxo-alcohols |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1230064B (en) * | 1989-04-18 | 1991-09-27 | Euron Spa | LUBRICANT FLUID FOR STEEL COLD ROLLING. |
-
1990
- 1990-10-19 IT IT02181290A patent/IT1243858B/en active IP Right Grant
-
1991
- 1991-10-07 ES ES91202610T patent/ES2048555T3/en not_active Expired - Lifetime
- 1991-10-07 EP EP91202610A patent/EP0482693B1/en not_active Expired - Lifetime
- 1991-10-07 DK DK91202610.1T patent/DK0482693T3/en active
- 1991-10-07 AT AT91202610T patent/ATE100488T1/en not_active IP Right Cessation
- 1991-10-07 DE DE69101047T patent/DE69101047T2/en not_active Expired - Fee Related
- 1991-10-08 AU AU85615/91A patent/AU640823B2/en not_active Ceased
- 1991-10-14 KR KR1019910018001A patent/KR940008391B1/en not_active IP Right Cessation
- 1991-10-17 MX MX9101625A patent/MX173927B/en unknown
- 1991-10-17 EC EC1991000786A patent/ECSP910786A/en unknown
- 1991-10-17 PL PL91292090A patent/PL167993B1/en not_active IP Right Cessation
- 1991-10-18 RU SU915001919A patent/RU2012591C1/en not_active IP Right Cessation
- 1991-10-18 CA CA002053691A patent/CA2053691C/en not_active Expired - Fee Related
- 1991-10-18 JP JP3297921A patent/JP3069872B2/en not_active Expired - Fee Related
- 1991-10-18 BR BR919104532A patent/BR9104532A/en not_active IP Right Cessation
- 1991-10-18 HU HU913300A patent/HU213625B/en not_active IP Right Cessation
- 1991-10-18 PT PT99284A patent/PT99284B/en not_active IP Right Cessation
- 1991-10-19 CN CN91109939A patent/CN1029006C/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2758975A (en) * | 1952-07-02 | 1956-08-14 | Exxon Research Engineering Co | Synthetic lubricants |
EP0089709A1 (en) * | 1982-03-19 | 1983-09-28 | AGIP PETROLI S.p.A. | Synthesis of higher alcohol carbonates and their use as synthetic lubricants |
EP0154363A1 (en) * | 1984-02-24 | 1985-09-11 | ENICHEM AUGUSTA S.p.A. | Process for separating linear-chain oxo-alcohols from mixtures of linear and branched-chain oxo-alcohols |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5562851A (en) * | 1994-12-21 | 1996-10-08 | Exxon Chemical Patents Inc. | Sulfur-containing carbonate reaction products as lubricating oil antiwear additives |
EP0987312A1 (en) * | 1998-08-22 | 2000-03-22 | Minebea Co., Ltd. | Bearing grease composition |
Also Published As
Publication number | Publication date |
---|---|
AU8561591A (en) | 1992-04-30 |
HUT59180A (en) | 1992-04-28 |
KR920008172A (en) | 1992-05-27 |
DE69101047D1 (en) | 1994-03-03 |
DE69101047T2 (en) | 1994-05-19 |
IT9021812A0 (en) | 1990-10-19 |
IT9021812A1 (en) | 1992-04-19 |
PT99284B (en) | 1999-04-30 |
CN1060866A (en) | 1992-05-06 |
ES2048555T3 (en) | 1994-03-16 |
ATE100488T1 (en) | 1994-02-15 |
MX173927B (en) | 1994-04-08 |
JPH04339895A (en) | 1992-11-26 |
HU913300D0 (en) | 1992-01-28 |
PL292090A1 (en) | 1992-04-21 |
PT99284A (en) | 1992-08-31 |
IT1243858B (en) | 1994-06-28 |
CA2053691C (en) | 2001-09-25 |
DK0482693T3 (en) | 1994-05-02 |
CA2053691A1 (en) | 1992-04-20 |
EP0482693B1 (en) | 1994-01-19 |
ECSP910786A (en) | 1992-07-23 |
HU213625B (en) | 1997-08-28 |
RU2012591C1 (en) | 1994-05-15 |
AU640823B2 (en) | 1993-09-02 |
CN1029006C (en) | 1995-06-21 |
BR9104532A (en) | 1992-06-09 |
KR940008391B1 (en) | 1994-09-14 |
JP3069872B2 (en) | 2000-07-24 |
PL167993B1 (en) | 1995-12-30 |
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