![]() LUBRICATING COMPOSITIONS FOR MOTOR VEHICLE
专利摘要:
The present invention relates to the field of lubricating compositions and base oils for motor vehicles. The invention provides a lubricating composition for an engine, gearbox or vehicle bridge. This lubricant composition comprises an oil soluble polymer which is a particular polyalkyl glycol or polyalkylene glycol (PAG). The invention also relates to the use of this lubricant composition for reducing the fuel consumption of a vehicle equipped with an engine, a bridge or a gearbox lubricated with this lubricating composition or this PAG. particular. 公开号:FR3024461A1 申请号:FR1457438 申请日:2014-07-31 公开日:2016-02-05 发明作者:Julien Sanson;Costa D Ambros Alder Da;Nadjet Khelidj 申请人:Total Marketing Services SA;Dow Global Technologies LLC; IPC主号:
专利说明:
[0001] The present invention relates to the field of lubricating compositions and base oils for motor vehicles. The invention provides a lubricating composition for an engine, gearbox or vehicle bridge. This lubricant composition comprises an oil soluble polymer which is a particular polyalkyl glycol or polyalkylene glycol (PAG). [0002] The invention also relates to the use of this lubricant composition for reducing the fuel consumption of a vehicle equipped with an engine, a bridge or a gearbox lubricated with this lubricating composition or this PAG. particular. Engine developments and performance of engine lubricating compositions are inextricably linked. The more the engines have a complex design, the higher the efficiency and the optimization of the consumption, the more the engine lubricating composition is solicited and must improve its performance. Very high compression in the engine, higher piston temperatures, particularly in the area of the upper piston ring, modern and maintenance-free valve controls with hydraulic lifters, and very high temperatures in the engine space demand increasingly lubricants for modern engines. The conditions of use of gasoline engines and diesel engines include extremely short journeys as well as long journeys. In fact, 80% of the journeys of Western European cars are less than 12 kilometers while vehicles cover annual mileages of up to 300 000 km. The emptying intervals are also very variable, from 5,000 km for some small diesel engines to up to 100,000 km on modern commercial diesel engines. [0003] Lubricating compositions for motor vehicles must therefore have improved properties and performance. Engine lubricating compositions must therefore fulfill many objectives that are sometimes contradictory. These objectives are derived from the five main functions of the engine lubricating compositions: lubrication, cooling, sealing, corrosion protection and pressure transmission. Lubrication of the parts sliding on each other plays a decisive role, in particular to reduce friction and wear, including fuel savings. Another essential requirement of engine lubricating compositions is related to the environmental aspects. It has indeed become essential to reduce oil consumption as well as fuel consumption, particularly in order to reduce emissions by 002. It is also important to reduce emissions of flue gases, for example by formulating oils. so that the catalyst remains perfectly functional throughout its service life. It is also important to limit or avoid the use of toxic additives in order to reduce or limit their elimination, for example by reprocessing or combustion. The nature of automotive engine lubricating compositions has an influence on pollutant emissions and fuel consumption. Engine lubricating compositions for energy-saving automobiles are often referred to as "fuel-eco" (FE) in English terminology. Such "fuel-eco" oils have been developed to meet these new needs. The reduction of energy losses is therefore a constant search in the field of automotive lubricants. For their part, gearbox or deck oils, and more generally gear oils, must meet numerous requirements, particularly those related to driving comfort (perfect gearshift, quiet operation, trouble-free operation, high reliability ), to the service life of the assembly (reduction of wear during cold passage, no deposits and high thermal stability, safety of lubrication at high temperatures, stable viscosity situation and absence of shear loss, long service life) and consideration of environmental aspects (lower fuel consumption, reduced oil consumption, low noise, easy evacuation). These are the requirements for manual transmission oils and axle gears. Concerning the requirements imposed on automatic gearbox oils (ATF oils for automatic transmission fluids), because of their use, it appears for ATF oils very specific requirements which are a great constancy of the coefficient of friction throughout the stay for optimal gear shifting, excellent aging stability for long emptying intervals, good viscosity-temperature performance to ensure perfect operation with a hot engine and a cold engine and sufficient sealing compatibility with various elastomers used in transmission seals so that they do not swell, shrink or embrittle. Moreover, in the automotive field, the search for the reduction of CO2 emissions requires the development of products that reduce friction in gearboxes and bridge differentials. This reduction of friction in the gearboxes and in the bridge differentials must be obtained for different operating conditions. These friction reductions must concern the internal friction of the lubricant but also the friction of the elements constituting the gearboxes or bridge differentials, in particular the metal elements. [0004] As vehicle transmission oils, refined petroleum products, hydrocracking oils or synthetic liquids, whether polyalphaolefins or esters, can be used. In some cases, polyglycols are also used, which generally have the disadvantage of not being or poorly miscible with other basic liquids. [0005] In order to achieve sufficient performance, vehicle transmission oils must also be supplemented with additives according to quality requirements, in particular high pressure additives. With regard to uses for vehicle engine lubrication, additives are also used. As coefficient-modifying additives, organometallic compounds, for example comprising molybdenum and in particular molybdenum sulphide, are commonly used. Molybdenum dithiocarbamates (MoDTC) can be mentioned as the major source of molybdenum. In addition, various viscosity index improvers (co) polymers in a lubricant composition are also known. It is necessary to provide alternative base oils, particularly oils having a high viscosity index (VI) as well as a low coefficient of traction. [0006] The desired lubricating compositions must have a high viscosity index in order to avoid cold energy losses due to friction but also to keep a sufficient lubricant film on the lubricated elements hot. A high viscosity index thus guarantees a lower drop in viscosity as the temperature increases. In a known manner, as lubricating compositions for vehicle engines, synthetic liquids are used, such as polyalphaolefin oils (PAO), esters and polyglycols; non-conventional mineral oils such as hydrocracked products; Conventional mineral oils; as well as their different mixtures. Thus, in the field of high VI bases with a low tensile coefficient, as lubricating compositions for vehicle engines, mixtures of PAO oils and esters are conventionally used, for example with a mass proportion of 'around 10 % ; mixtures of PAO oils and hydrocracked and hydroisomerized oils (group III or Gp III) or mixtures of PAO oils and hydrocracked and hydroisomerized oils with additives or base oils GTL (gasto- liquid or oils obtained from liquefied natural gas, for example by Fisher-Tropsch processes). Furthermore, it is common to encounter solubility problems when using PAG of the state of the art. The use of the PAGs of the state of the art is therefore generally limited to certain applications as industrial oils and not as engine oils or vehicle transmission. There is therefore a need to provide motor and vehicle transmission oils and lubricant compositions which provide a solution to some or all of the problems of the prior art lubricating oils or compositions. Thus, the invention provides a lubricating composition comprising at least one oil of formula (I) OCH3 (I) wherein - R represents a linear or branched C1-C30 alkyl group; m and n independently represent an average number ranging from 1 to 5. Preferably, the lubricating composition according to the invention comprises at least one oil of formula (I) in which R represents a group chosen from a linear C5-alkyl group ; a branched C5-alkyl group; a linear C9-alkyl group; a branched C9-alkyl group; a linear C10-alkyl group; a C10-branched alkyl group; a linear C11-alkyl group; a C11-branched alkyl group; a linear C12-alkyl group; a C12-branched alkyl group; a linear C13-alkyl group; a C13-branched alkyl group; a linear C14-alkyl group; a C14-branched alkyl group; a linear C15-alkyl group; a branched C15-alkyl group. More preferably, the lubricating composition according to the invention comprises at least one oil of formula (I) in which R represents a branched C5-alkyl group or a linear C12-alkyl group. [0007] Even more preferably, the lubricant composition according to the invention comprises at least one oil of formula (I) in which R represents a linear C12-alkyl group. Also preferably, the lubricating composition according to the invention comprises at least one oil of formula (I) in which m is greater than or equal to n; or ^ m represents an average number ranging from 2 to 4.5; where n represents an average number ranging from 1.5 to 4. [0008] As examples of preferred lubricant compositions according to the invention, there may be mentioned a lubricating composition comprising at least one oil of formula (I) in which m represents an average number ranging from 2.5 to 3.5; where n represents an average number ranging from 2 to 3. [0009] As examples of lubricant compositions that are particularly preferred according to the invention, mention may be made of a lubricating composition comprising at least one oil of formula (I) in which m represents an average number of 2.5 and n represents an average number of 2 ; where m represents an average number equal to 3.5 and n represents an average number equal to 2.8. As other examples of preferred lubricant compositions according to the invention, there may be mentioned a lubricating composition comprising at least one oil of formula (I) in which R represents a branched C8-alkyl group, m represents an average number ranging from 2 to 4 , 5, and n represents an average number ranging from 1.5 to 4; or R represents a branched C8-alkyl group, m represents an average number ranging from 2.5 to 3.5 and n represents an average number ranging from 2 to 3. As further examples of lubricant compositions that are particularly preferred according to the invention, mention may be made of a lubricating composition comprising at least one oil of formula (I) in which R represents a linear C12-alkyl group, m represents an average number ranging from 2 to 4.5, and n represents an average number ranging from 1 , 5 to 4; or R represents a linear C12-alkyl group, m represents an average number ranging from 2.5 to 3.5 and n represents an average number ranging from 2 to 3. [0010] As examples of lubricant compositions which are also preferred according to the invention, mention may be made of a lubricating composition comprising at least one oil of formula (I) in which R represents a C8-branched alkyl group, m represents an average number of 2.5 and n represents an average number equal to 2; or R represents a branched C8-alkyl group, m represents an average number equal to 3.5 and n represents an average number equal to 2.8. As examples of lubricant compositions that are very particularly preferred according to the invention, mention may be made of a lubricating composition comprising at least one oil of formula (I) in which R represents a linear C 12 -alkyl group, m represents an average number equal to 2, And n represents an average number equal to 2; or R represents a linear C12-alkyl group, m represents an average number equal to 3.5 and n represents an average number equal to 2.8.35. Preferably, the lubricating composition according to the invention comprises at least one oil of formula (I) of which (a) the kinematic viscosity at 100 ° C, measured according to ASTM D445, ranges from 2.5 to 4.5 mm 2 s -1; or (b) the viscosity number is greater than 160 or is between 160 and 210; or (c) the pour point is less than -40 ° C, or (d) the dynamic viscosity (CCS) at -35 ° C measured by ASTM D5293 is less than 1,200 mPa.s. [0011] In general, according to the invention, the viscosity number is calculated according to ASTM D2270 and the pour point is measured according to EN ISO 3016. More preferably, the lubricating composition according to the invention comprises at least an oil of formula (I) wherein (a) the kinematic viscosity at 100 ° C, measured according to ASTM D445, is from 2.5 to 4.5 mm 2 s -1; (b) the viscosity number is greater than 160 or is between 160 and 210; (c) the pour point is less than -40 ° C; (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 1200 mPa.s. In a particularly preferred manner, the lubricating composition according to the invention comprises at least one oil of formula (I) in which m represents an average number equal to 2.5 and n represents an average number equal to 2 and of which (a) the viscosity Kinematic at 100 ° C, measured according to ASTM D445, ranges from 2.5 to 3.5 mm 2 s -1; or (b) the viscosity number is between 160 and 180; or (c) the pour point is less than -40 ° C, or (d) the dynamic viscosity (CCS) at -35 ° C measured by ASTM D5293 is less than 500 mPa.s. Also particularly preferably, the lubricant composition according to the invention comprises at least one oil of formula (I) in which m represents an average number equal to 2.5 and n represents an average number equal to 2 and of which (a) the Kinematic viscosity at 100 ° C, measured according to ASTM D445, is 2.5 to 3.5 mm 2 s -1; (b) the viscosity number is between 160 and 180; (c) the pour point is less than -40 ° C; (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 500 mPa.s. Also particularly preferably, the lubricating composition according to the invention comprises at least one oil of formula (I) in which m represents an average number equal to 3.5 and n represents an average number equal to 2.8 and of which (a) ) the kinematic viscosity at 100 ° C, measured according to ASTM D445, ranges from 3.5 to 4.5 mm 2 s -1; or (b) the viscosity number is between 180 and 210; or (c) the pour point is less than -50 ° C, of which (d) the dynamic viscosity (CCS) at -35 ° C measured by ASTM D5293 is less than 1,200 mPa.s. Also particularly preferably, the lubricating composition according to the invention comprises at least one oil of formula (I) in which m represents an average number equal to 3.5 and n represents an average number equal to 2.8 and of which (a) ) the kinematic viscosity at 100 ° C, measured according to ASTM D445, is from 3.5 to 4.5 mm 2 s -1; (b) the viscosity number is between 180 and 210; (c) the pour point is less than -50 ° C; (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 1200 mPa.s. Advantageously, the lubricating composition according to the invention comprises from 2 to 60% by weight of at least one oil of formula (I); or 2 to 50% by weight of at least one oil of formula (I); or 5 to 40% by weight of at least one oil of formula (I); or 5 to 30% by weight of at least one oil of formula (I). A preferred example of a lubricant composition according to the invention comprises from 5 to 40% by weight, preferably from 10 to 35% by weight or from 15 to 25% by weight, of at least one oil of formula (I) in which m represents a mean number equal to 2.5 and n represents an average number equal to 2 and whose kinematic viscosity at 100 ° C., measured according to the ASTM D445 standard, ranges from 2.5 to 3.5 mm 2 s -1; the viscosity number is between 160 and 180; the pour point is less than -40 ° C; the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 500 mPa.s. [0012] Another preferred example of a lubricating composition according to the invention comprises from 5 to 35% by weight, preferably from 8 to 30% by weight or 10% by weight, 20% by weight or 30% by weight, of at least one an oil of formula (I) in which m represents an average number equal to 3.5 and n represents an average number equal to 2.8 and of which (a) the kinematic viscosity at 100 ° C., measured according to the ASTM D445 standard, is from 3.5 to 4.5 mm2s-1; (b) the viscosity number is between 180 and 210; (c) the pour point is less than -50 ° C; (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 1200 mPa.s. [0013] Advantageously, the lubricating composition according to the invention also comprises at least one other base oil chosen from group III oils, group IV oils and group V oils; or at least one additive; or at least one other base oil selected from Group III oils, Group IV oils and Group V oils and at least one additive. In general, the lubricating composition according to the invention may comprise any type of mineral lubricating base stock, synthetic or natural, animal or vegetable adapted to their use. The base oils used in the lubricant compositions according to the invention may be oils of mineral or synthetic origins belonging to groups I to V according to the classes defined in the API classification (or their equivalents according to the ATIEL classification) (Table A) or their mixtures. [0014] Content in saturated sulfur content viscosity (VI) Group I Mineral oils <90%> 0.03% 80 VI <120 Group II 90 (3/0 0.03 (3/0 80 VI <120 Hydrocracked oils Group III 90% 0.03% 120 Hydrocracked or hydro-isomerized oils Group IV Polyalphaolefines (PAO) Group V Esters and other bases not included in groups I to IV Table A The mineral base oils according to the invention include all types of bases obtained by atmospheric and vacuum distillation of crude oil, followed by refining operations such as solvent extraction, desalting, solvent dewaxing, hydrotreating, hydrocracking, hydroisomerization and hydrofinishing Mixtures of synthetic and mineral oils may also be employed. There is generally no limitation as to the use of different lubricating bases for producing the lubricating compositions according to the invention, except that they must have properties, in particular of viscosity, viscosity index, sulfur content, oxidation resistance, adapted for use for engines or for vehicle transmissions. The base oils of the lubricating compositions according to the invention may also be chosen from synthetic oils, such as certain carboxylic acid esters and alcohols, and from polyalphaolefins. The polyalphaolefins used as base oils are, for example, obtained from monomers comprising from 4 to 32 carbon atoms, for example from octene or decene, and whose viscosity at 100 ° C. is between 1.5 and 15 mm2.s-1 according to ASTM D445. Their average molecular weight is generally between 250 and 3000 according to ASTM D5296. [0015] Advantageously, the lubricant composition according to the invention comprises at least 50% by weight of base oils relative to the total mass of the composition. [0016] More advantageously, the lubricating composition according to the invention comprises at least 60% by weight, or even at least 70% by weight, of base oils relative to the total mass of the composition. More particularly advantageously, the lubricating composition according to the invention comprises from 75 to 99.9% by weight of base oils relative to the total mass of the composition. The invention also provides a lubricant composition for a motor vehicle comprising at least one lubricating composition according to the invention, at least one base oil and at least one additive. Many additives can be used for this lubricant composition according to the invention. The preferred additives for the lubricant composition according to the invention are chosen from detergent additives, anti-wear additives, friction modifying additives, extreme pressure additives, dispersants, pour point improvers, anti-wear agents and anti-wear agents. foam, thickeners and mixtures thereof. Preferably, the lubricating composition according to the invention comprises at least one antiwear additive, at least one extreme pressure additive or their mixtures. Anti-wear additives and extreme pressure additives protect friction surfaces by forming a protective film adsorbed on these surfaces. There is a wide variety of anti-wear additives. In a preferred manner for the lubricating composition according to the invention, the anti-wear additives are chosen from phosphosulfur additives such as metal alkylthiophosphates, in particular zinc alkylthiophosphates, and more specifically zinc dialkyldithiophosphates or ZnDTPs. The preferred compounds have the formula Zn ((SP (S) (OR1) (OR2)) 2, in which R1 and R2, which may be identical or different, independently represent an alkyl group, preferably an alkyl group comprising from 1 to 18 carbon atoms. The amine phosphates are also anti-wear additives which can be used in the lubricating composition according to the invention However, the phosphorus provided by these additives can act as a poison for the catalytic systems of automobiles because these additives are ash generators. These effects can be minimized by partially replacing the amine phosphates with non-phosphorus additives, such as, for example, polysulfides, especially sulfur-containing olefins. comprise from 0.01 to 6% by weight, preferably from 0.05 to 4% by weight, more preferably from 0.1 to 2% by weight relative to the total weight lubricating composition, anti-wear additives and extreme pressure additives. Advantageously, the lubricant composition according to the invention may comprise at least one friction-modifying additive. The friction modifying additive may be chosen from a compound providing metal elements and an ash-free compound. Among the compounds providing metal elements, mention may be made of transition metal complexes such as Mo, Sb, Sn, Fe, Cu and Zn, the ligands of which may be hydrocarbon compounds comprising oxygen, nitrogen, sulfur or phosphorus. The ashless friction modifier additives are generally of organic origin and may be selected from monoesters of fatty acids and polyols, alkoxylated amines, alkoxylated fatty amines, fatty epoxides, borate fatty epoxides; fatty amines or fatty acid glycerol esters. According to the invention, the fatty compounds comprise at least one hydrocarbon group comprising from 10 to 24 carbon atoms. [0017] Advantageously, the lubricating composition according to the invention may comprise from 0.01 to 2% by weight or from 0.01 to 5% by weight, preferably from 0.1 to 1.5% by weight or 0.1 at 2% by weight relative to the total mass of the lubricant composition, friction modifier additive. [0018] Advantageously, the lubricant composition according to the invention may comprise at least one antioxidant additive. The antioxidant additive generally serves to retard the degradation of the lubricating composition in service. This degradation can notably result in the formation of deposits, the presence of sludge or an increase in the viscosity of the lubricant composition. Antioxidant additives act in particular as radical inhibitors or destroyers of hydroperoxides. Among the antioxidant additives commonly used, mention may be made of antioxidant additives of phenolic type, antioxidant additives of amine type, antioxidant phosphosulfur additives. Some of these antioxidant additives, for example phosphosulfur antioxidant additives, can be ash generators. Phenolic antioxidant additives may be ash-free or may be in the form of neutral or basic metal salts. The antioxidant additives may especially be chosen from sterically hindered phenols, sterically hindered phenol esters and sterically hindered phenols comprising a thioether bridge, diphenylamines, diphenylamines substituted by at least one C 1 -C 12 alkyl group, and N, N '-dialkyl-aryl diamines and mixtures thereof. Preferably, according to the invention, the sterically hindered phenols are chosen from compounds comprising a phenol group in which at least one vicinal carbon of the carbon bearing the alcohol function is substituted by at least one alkyl group at 0, - 010, preferably a grouping. C 1 -C 6 alkyl, preferably a C 4 -C 4 alkyl group, preferably with the ter-butyl group. Amino compounds are another class of antioxidant additives that can be used, optionally in combination with phenolic antioxidant additives. Examples of amine compounds are aromatic amines, for example aromatic amines of formula NR1R2R3 in which R1 represents an optionally substituted aliphatic or aromatic group, R2 represents an optionally substituted aromatic group, R3 represents a hydrogen atom, an alkyl group, an aryl group or a group of formula R4S (O), R5 in which R4 represents an alkylene group or an alkenylene group, R5 represents an alkyl group, an alkenyl group or an aryl group and z represents 0, 1 or 2. Sulfurized alkyl phenols or their alkali and alkaline earth metal salts can also be used as antioxidant additives. [0019] Another class of antioxidant additives is copper compounds, for example copper thio- or dithio-phosphates, copper and carboxylic acid salts, dithiocarbamates, sulphonates, phenates, copper acetylacetonates. Copper salts I and II, succinic acid or anhydride salts can also be used. [0020] The lubricant composition according to the invention may contain all types of antioxidant additives known to those skilled in the art. Advantageously, the lubricating composition comprises at least one ash-free antioxidant additive. Also advantageously, the lubricating composition according to the invention comprises from 0.5 to 2% by weight relative to the total weight of the composition, of at least one antioxidant additive. The lubricant composition according to the invention may also comprise at least one detergent additive. [0021] The detergent additives generally make it possible to reduce the formation of deposits on the surface of the metal parts by dissolving the secondary oxidation and combustion products. The detergent additives that can be used in the lubricant composition according to the invention are generally known to those skilled in the art. The detergent additives may be anionic compounds comprising a long lipophilic hydrocarbon chain and a hydrophilic head. The associated cation may be a metal cation of an alkali metal or alkaline earth metal. The detergent additives are preferably chosen from the alkali metal or alkaline earth metal salts of carboxylic acids, the sulphonates, the salicylates, the naphthenates and the phenate salts. The alkali and alkaline earth metals are preferably calcium, magnesium, sodium or barium. These metal salts generally comprise the metal in stoichiometric quantity or in excess, therefore in an amount greater than the stoichiometric amount. It is then overbased detergent additives; the excess metal bringing the overbased character to the detergent additive is then generally in the form of an oil insoluble metal salt, for example a carbonate, a hydroxide, an oxalate, an acetate, a glutamate, preferably a carbonate . Advantageously, the lubricant composition according to the invention may comprise from 2 to 4% by weight of detergent additive relative to the total mass of the lubricating composition. Also advantageously, the lubricant composition according to the invention may also comprise at least one pour point depressant additive. [0022] By slowing the formation of paraffin crystals, pour point depressant additives generally improve the cold behavior of the lubricant composition according to the invention. As examples of pour point depressant additives, mention may be made of alkyl polymethacrylates, polyacrylates, polyarylamides, polyalkylphenols, polyalkylnaphthalenes and alkylated polystyrenes. Advantageously, the lubricant composition according to the invention may also comprise at least one dispersing agent. The dispersing agent may be selected from Mannich bases, succinimides and their derivatives. [0023] Also advantageously, the lubricating composition according to the invention may comprise from 0.2 to 10% by weight of dispersing agent relative to the total mass of the lubricating composition. [0024] Advantageously, the lubricating composition may also comprise at least one additional polymer improving the viscosity index. This additional polymer is generally different from the oil soluble polymer selected from polyalkylene glycols (PAG). As examples of additional viscosity index improving polymers, there may be mentioned polymeric esters, homopolymers or copolymers, hydrogenated or non-hydrogenated, styrene, butadiene and isoprene, polymethacrylates (PMA). Also advantageously, the lubricating composition according to the invention may comprise from 1 to 15% by weight relative to the total weight of the oil-soluble polymer lubricating composition chosen from polyalkylene glycols (PAG) and from additional polymer improving the viscosity index. The lubricating composition according to the invention can be in various forms. The lubricant composition according to the invention may in particular be an anhydrous composition. Preferably, this lubricating composition is not an emulsion. [0025] The invention also relates to the use of the lubricant composition according to the invention for reducing the fuel consumption of an engine, in particular a vehicle engine. [0026] The invention also relates to the use of the lubricant composition according to the invention for reducing the traction coefficient of a vehicle engine oil. The invention also relates to the use of the lubricant composition according to the invention for reducing the fuel consumption of a vehicle equipped with a bridge or a gearbox lubricated with this composition. The invention also relates to the use of the lubricant composition according to the invention for reducing the fuel consumption of a vehicle equipped with a transmission lubricated with this composition. The invention also relates to the use of the composition lubricant according to the invention to reduce the traction coefficient of a transmission oil, in particular a gearbox oil or a deck oil. [0027] The invention also relates to the use of at least one oil of formula (I) according to the invention for improving the Fuel Eco (FE) of a lubricant. The invention also relates to the use of at least one oil of formula (I) according to the invention for reducing the fuel consumption of an engine, in particular a vehicle engine. The invention also relates to the use of at least one oil of formula (I) according to the invention for reducing the traction coefficient of a vehicle engine oil. [0028] The invention also relates to the use of at least one oil of formula (I) according to the invention for reducing the fuel consumption of a vehicle equipped with a bridge or a gearbox lubricated by means of this invention. oil. The invention also relates to the use of at least one oil of formula (I) according to the invention for reducing the fuel consumption of a vehicle equipped with a transmission lubricated with this oil. The invention also relates to the use of at least one oil of formula (I) according to the invention for reducing the traction coefficient of a transmission oil, in particular a gearbox oil or a gearbox. deck oil. According to the invention, the oil of formula (I) and the lubricating composition can be used for the lubrication of a vehicle engine. [0029] These uses of the lubricant composition according to the invention or of the oil of formula (I) comprise contacting at least one element of the engine, of the transmission, in particular of the gearbox or the bridge, with a lubricating composition according to the invention or with an oil of formula (I). [0030] By analogy, the particular, advantageous or preferred characteristics of the oil of formula (I) according to the invention or of the lubricating composition according to the invention define particular, advantageous or preferred uses according to the invention. [0031] The invention also relates to a method for preparing the lubricant composition according to the invention from at least one oil of formula (I) M (I) in which R represents a linear or branched C1-C30-alkyl group; m and n independently represent an average number of 1 to 5. The oil of formula (I) is generally prepared from an initiating alcohol of formula R-OH mixed with a solution of an alkali metal hydroxide or alkaline earth metal. As the initiator alcohol, 2-ethyl-hexanol and dodecanol are preferred. As the alkali or alkaline earth metal hydroxide, potassium hydroxide is preferred. Under an inert atmosphere, a mixture of at least one initiating alcohol and at least one alkaline earth metal hydroxide is heated to a temperature of from 80 to 130 ° C, for example about 115 ° C. Then, the water present in the medium is removed, for example by flash evaporation, in order to limit the presence of water, for example at a concentration of less than 0.1% by weight. Then, 1,2-propylene oxide and 1,2-butylene oxide are introduced at a temperature ranging from 90 to 150 ° C., for example about 130 ° C., and at a pressure to go from 350 to 550 kPa. It is stirred and allowed to act for 5 to 25 hours. The residual catalyst is then separated, for example by filtration through magnesium silicate. An intermediate product of formula (II) in which R is a linear or branched C1-C30 alkyl group is obtained; m and n independently represent an average number ranging from 1 to 5. [0032] Then, the intermediate product of formula (II) is reacted in the presence of a solution of alkali or alkaline earth metal alkoxide in an alcohol, for example methanol, at a temperature ranging from 80 to 140 ° C. for example at 120 ° C, and at reduced pressure, for example less than 1 kPa, and under an inert atmosphere. As the alkali or alkaline earth metal alkoxide, sodium methoxide is preferred. [0033] An alkyl halide is added and, under an inert atmosphere, it is allowed to act at a temperature ranging from 50 to 130 ° C., for example 80 ° C., at a pressure that may range from 120 to 350 kPa, for example 260 kPa, and for 5 to 25 hours. As alkyl halide, methyl chloride is preferred. It is stirred and allowed to act for 15 minutes to 15 hours, for example for 1.5 hours, and at a temperature ranging from 50 to 130 ° C., for example 80.degree. ° C. Then, the alkyl ether formed and the unreacted alkyl halide are separated, for example by flash evaporation. The alkali metal or alkaline earth metal halide is washed, for example with water. The aqueous salt phase is separated, for example by decantation. Then, the residual water is separated, for example with magnesium silicate and flash evaporation. The mixture can be allowed to cool and then filtered, for example with magnesium silicate, to obtain the oil of formula (I) according to the invention. The oil of formula (I) according to the invention can be incorporated with one or more other base oils and one or more additives to form the lubricating composition according to the invention. The various aspects of the invention are illustrated by the following examples. EXAMPLE 1 Preparation of a PAG Oil of Formula (I) According to the Invention - Oil (1) C'ZH2 ro average values: m = 3.53 and n = 2.84 In a stainless steel autoclave reactor, dodecanol (2647 g) is introduced as an initiator and then a 45% by weight solution of potassium hydroxide (28.2 g). The mixture is heated to 115 ° C under a helper atmosphere. Then, the water is removed by flash evaporation (115 ° C., 3 MPa) to a water concentration of less than 0.1% by weight. A mixture of 1,2-propylene oxide (2910 g) and 1,2-butylene oxide (2910 g) was introduced into the reactor at a temperature of 130 ° C. and a pressure of 490 kPa. . It is stirred and allowed to act for 14 hours at 130 ° C. The residual catalyst is separated by filtration through magnesium silicate at 50 ° C. to obtain the intermediate product (A) whose kinematic viscosity measured at 40 ° C. according to ASTM D445 is 22.4 mm 2 .s -1, the kinematic viscosity measured at 100 ° C. according to ASTM 445 is 4.76 mes-1, the viscosity index is 137 and the pour point is -48 ° C. [0034] In a stainless steel autoclave reactor, product (A) (8,266 g) was introduced. A solution of 25% by weight sodium methoxide in methanol (3060 g) was added and stirred (180 rpm) at 120 ° C for 12 hours at reduced pressure (<1 kPa) with nitrogen flow (200 mL per minute). Methyl chloride (751 g) was added at 80 ° C and under pressure (260 kPa). [0035] The mixture is stirred and allowed to act for 1.5 hours at 80 ° C. Then, flash evaporation (10 min, 80 ° C, reduced pressure) was carried out to separate the dimethyl ether and the unreacted methyl chloride. Water (2555g) was added and then stirred for 40 minutes at 80 ° C to wash the sodium chloride from the mixture. Stirring is stopped and allowed to stand for 1 hour at 80 ° C. The aqueous saline phase is separated by decantation (3283 g), magnesium silicate (50 g) is added to the remaining mixture and flash evaporation is carried out (1 hour, 100 ° C., at a pressure of less than 1 kPa flow of nitrogen (200 mL per minute) and stirring (180 rpm) to separate the residual water. [0036] The mixture is allowed to cool to 60 ° C and then is run through magnesium silicate at 50 ° C to separate the oil (1) (8,359 g). The yield of the methylation step is 98.6% by weight. For this oil (1), the kinematic viscosity measured at 40 ° C. according to ASTM D445 is 14.4 mm 2s -1, the kinematic viscosity measured at 100 ° C. according to ASTM D445 is 3.98 mm 2. .s-1 and the pour point measured according to ISO 3016 is -54 ° C. The viscosity index of this oil is 194 and its dynamic viscosity (CCS) at -35 ° C., measured according to the ASTM D5293 standard, is 1,120 mPa.s. [0037] EXAMPLE 2 Preparation of a PAG Oil of Formula (I) According to the Invention - Oil (2) C12 H25 0 ° OCH3 average values: m = 2.45 and n = 1.97 In a stainless steel autoclave reactor, dodecanol (2369 g) is introduced as an initiator and then a 45% by weight solution of potassium hydroxide (20.02 g). The mixture is heated to 115 ° C under a nitrogen atmosphere. Flash evaporation (115 ° C. and 3 MPa) of the mixture is carried out to separate the water. The water concentration of the mixture is lowered to less than 0.1% by weight. A mixture of 1,2-propylene oxide (1,808.5 g) and 1,2-butylene oxide (1,808.5 g) was introduced into the reactor at a temperature of 130 ° C. and a pressure of 490 kPa. It is stirred and allowed to act for 14 hours at 130 ° C. The residual catalyst is separated by filtration through magnesium silicate at 50 ° C to obtain the intermediate product (B) whose kinematic viscosity measured at 40 ° C according to ASTM D445 is 16.1 mm 2 s -1, the kinematic viscosity measured at 100 ° C. according to ASTM D445 is 3.7 nm 2 · s -1 and the pour point of -39 ° C. In a stainless steel autoclave reactor, the product is introduced ( B) (5,797 g) A solution of 25% by weight sodium methoxide in methanol (2,765 g) is added and stirred (180 rpm) at 120 ° C for 12 hours under reduced pressure 25 (less than 1 kPa) with a stream of nitrogen (200 mL per minute) One part of the mixture (3825 g) is emptied from the reactor and then into the other part of the mixture (2264 g) which remains in To the reactor, methyl chloride (252 g) was added at 80 ° C. and under pressure (260 kPa), the mixture was stirred and allowed to act for 1.5 hours at 80 ° C. Flash evaporation (10 min., 80 ° C, reduced pressure) to remove dimethyl ether and unreacted methyl chloride. [0038] Water (796 g) is added and then stirred for 40 minutes at 80 ° C to wash the sodium chloride from the mixture. Stirring is stopped and allowed to stand for 1 hour at 80 ° C. The aqueous salt phase (961 g) is separated by decantation, magnesium silicate (50 g) is added to the remaining mixture and flash evaporation is carried out (1 hour, 100 ° C., at a pressure of less than 1 kPa) under one hour. nitrogen flow (200 mL per minute) and stirring (180 rpm). The mixture was allowed to cool to 60 ° C and then filtered through magnesium silicate at 50 ° C to separate the oil (2) (2218 g). The yield of the methylation step is 93.7% by weight. For this oil (2), the kinematic viscosity measured at 40 ° C. according to the ASTM D445 standard is 9.827 mm 2s -1, the kinematic viscosity measured at 100 ° C. according to the ASTM D445 standard is 2.97 mm 2. -1 and the pour point measured according to ISO 3016 is -48 ° C. The viscosity number of this oil is 172 and its dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293, is 450 mPa.s. Comparative Example 3: Preparation of a Known PAG Oil - Comparative Oil (1) C12 H20 + - 0 + average values: m = 1.76 and n = 1.42 In a stainless steel autoclave reactor, Dodecanol (4,364 g) was introduced as initiator and then a solution of 45% by weight of potassium hydroxide (39.68 g), the mixture was heated at 115 ° C. under a nitrogen atmosphere. 115 ° C. and 3 MPa) of the mixture to separate the water, the water concentration of the mixture is lowered to 0.1% by weight, and 1,2-propylene oxide (2,276 m 2) is introduced into the reactor. g) and 1,2-butylene oxide (2,276 g) at a temperature of 130 ° C and a pressure of 370 kPa, stirred and allowed to react for 12 hours at 130 ° C. residual catalyst by filtration through magnesium silicate at 50 ° C to obtain the comparative oil (1) whose kinematic viscosity measured at 40 ° C according to ASTM D445 is 12.2 mm2 .s1, the kinematic viscosity measured at 100 ° C according to ASTM D445 is 3.0 mm2.s-1 and the pour point of -29 ° C. The viscosity number of this oil is 60 and its dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293, is 4090 mPa.s. Comparative Example 4: Preparation of a Known PAG Oil - Comparison Oil (2) Average Values: m = 2.79 and n = 2.25 In a stainless steel autoclave reactor, dodecanol (3141 g) was introduced as the initiator then a solution of 45% by weight of potassium hydroxide (38.4 g). The mixture is heated to 115 ° C under a nitrogen atmosphere. Flash evaporation (115 ° C. and 3 MPa) of the mixture is carried out to separate the water. The water concentration of the mixture is lowered to 0.1% by weight. A mixture of 1,2-propylene oxide (2,735.5 g) and 1,2-butylene oxide (2,735.5 g) at a temperature of 130 ° C. and a pressure of 370 kPa. It is stirred and allowed to act for 12 hours at 130 ° C. [0039] The residual catalyst is separated by filtration through magnesium silicate at 50 ° C to obtain the comparative oil (2) whose kinematic viscosity measured at 40 ° C. according to ASTM D445 is 18.0 mm 2 .s -1 the kinematic viscosity measured at 100 ° C according to ASTM D445 is 4.0 mm2s-1 and the pour point of -41 ° C. The viscosity number of this comparative oil (2) is 116 and its dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293, is 3,250 mPa.s. Example 5: Preparation of lubricating compositions according to the invention, comparative lubricating compositions and evaluation of the properties of these compositions for lubricating the transmission of a motor vehicle The lubricating compositions are prepared by mixing the oil (2) according to Example 2 and known oils with other base oils and with additives for the preparation of lubricating compositions according to the amounts (% by weight) of Table 1. Composition (1) according to the invention Composition (2) according to Comparative Composition (1) Base Oil Group III (KV100 / ASTM D445 = 3) 20.0 / 40.75 Base Oil Group III (KV100 / ASTM D445 = 4) 41.75 43.3 41.0 oil (2) according to the invention 20.0 38.45 / viscosity index improving additive (polymethacrylate - PMA) 6.0 6.0 6.0 viscosity improving additive (polyethylene-polypropylene - PEPP) 5 5.0 5.0 additive mixture (dispersant, detergent, antioxidant, extreme ssion, anti-wear, anti-foaming) 7.0 7.0 7.0 friction reducing additive (organo-molybdenum) 0.2 0.2 0.2 silicone antifoam additive 0.05 0.05 0, Table 1 The characteristics of the lubricating compositions prepared are evaluated and the results obtained are shown in Table 2. Composition (1) according to the invention Composition (2) according to the invention Comparative composition (1) Viscosity index (ISO 2909) 197 205 185 traction coefficient (MTM: 0.045 0.043 0.053 T = 40 ° C, Ve = 1 m / s, SRR = 20% load = 75 N) Energy efficiency deviation from commercial oil 0.20 0.21 0.06 oxidation resistance (CEC 1517) (160 ° C - 192 h) variation KV 40 (%) -5.0 8.6 21.01 variation KV100 (%) 5.4 4.3 18.95 variation of TAN (mg KOH / g) amount of insoluble matter (% by mass) 0,23 0,22 1,3 0,0012 0,0032 0,004 compatibility elastomers hardness variation for RE1 fluorocarbon 2 1 3 RE2 polyacrylate ACM 1 - 3 -2 HNBR1 -1 -3 1 75FKM595 8 9 ND t is wear 4 balls (4B4 PSA D55-1078 / RENAULT D55 1994) wear diameter (mm) 0.80 0.74 0.73 extreme pressure test 4 balls (4B6 ASTM D551136) 0.47 0.46 ND wear diameter before seizing (mm) 90 90 ND - last load before 1.36 0.87 ND seizing (kg) wear diameter at first seizure (mm) - first seizing load 120 120 ND systematic (kg) ND: not available Table 2 Energy efficiency is evaluated by comparison with commercial oil for gearboxes based on Group III oils (KV100 = 7.46 mm2.s-1, KV40 = 33.97 mm2s-1 , vi = 196). The difference in energy yield between the evaluated compositions and this commercial oil is measured. This test therefore makes it possible to evaluate the energy efficiency and to quantify the efficiency of the gearbox used by comparing the output torque with the input torque. [0040] It is thus possible to evaluate the Fuel Eco property of the gearbox oils used. In this test, a five-speed manual gearbox was used. The oil temperatures are 20 ° C and 50 ° C. They make it possible to differentiate the oils by their Fuel Eco properties, especially when cold (20 ° C). The input torque is set at 30 Nm and then at 90 Nm. The input speed is set at 1000 rpm and then 3000 rpm. For each oil temperature and for each gear ratio, the operating conditions are shown in Table B. Gearbox Temperature Torque at the Inlet Speed at the Inlet (RPM) Oil (° C) (Nm) 20 R2 30 1,000 90 3,000 30 1,000 90 3,000 R3 30 1,000 90 3,000 30 1,000 90 3,000 50 R4 30 1,000 90 3,000 30 1,000 90 3,000 R5 30 1,000 90 3 000 30 1 000 90 3 000 Table B This test is used to simulate a European NEDC test and to determine the CO2 emission and fuel consumption of a gearbox lubricated with a particular oil. The higher the efficiency value, the better the reduction in fuel consumption. [0041] Thus, it can be seen that compared to a lubricating composition comprising two Group III oils of the state of the art, the lubricating compositions comprising the oil (2) according to the invention have improved properties. [0042] The viscosity index is much higher. The traction coefficient is lowered by at least 7 `Vo. The energy efficiency is also greatly improved and allows a gain more than 3 times higher than a composition based on a commercial oil based on Group III oils. These parameters therefore make it possible to demonstrate the Fuel Eco gain of the composition according to the invention. The lubricant compositions according to the invention also have an oxidation resistance which is of the same level or even higher than that of the lubricant composition of the state of the art. Their compatibility with the various elastomers that can be used in the transmission joints with which they are in contact is also at the same level or better than that of the lubricant composition of the state of the art. In addition, the compositions according to the invention allow a good wear resistance of the mechanical parts of a car transmission. Finally, it can be seen that the improvements in the properties of the lubricating composition comprising 20% of oil (2) according to the invention are of the same order or even greater than those of the lubricating composition comprising 38.45% of oil (2) according to the invention. 'invention. EXAMPLE 6 Preparation of lubricating compositions according to the invention, comparative lubricating compositions and evaluation of the properties of these compositions for lubricating a vehicle engine The lubricating compositions are prepared by mixing the oil (1) according to the example 1 and known oils with other base oils and with additives for the preparation of lubricating compositions according to the amounts (°) / 0 by mass) of Table 3. Composition (3) according to the invention Composition (4) according to the invention Comparative Composition (2) Base Oil Group III (KV100 / ASTM D445 = 4.16 mm2.s-1) 45.45 37.45 37.45 Base Oil Group III: Neste Nexbase 3050 29.0 17, 3 15.0 base oil group IV PAO (KV100 / ASTM D445 = 4.08 mm2.s-1) / / 30.0 oil (1) according to the invention 8.0 27.7 / mixture of additives ( dispersants, 10.9 10.9 10.9 detergent, DTPZn, antioxidant amine, phenolic antioxidant) viscosity index improver additive (polyisoprene-styrene h ydrogéné - PISH) 3.2 3.2 3.2 viscosity index improver additive (PMA) 2.9 2.9 2.9 friction reducing additive (MoDTC) 0.5 0.5 0.5 additive The characteristics of the lubricating compositions prepared are evaluated and the results obtained are shown in Table 4. Composition (3) according to the invention Composition (4) according to the invention Comparative Composition (2) viscosity index (ISO 2909) 192 202 190 Noack volatility (CEC L-40-93) (%) 10.3 9.5 10.4 dynamic viscosity (CCS) at -35 ° C ( ASTM D5293) (mPa. $) 6,790 4,970 4,970 oxidation resistance (GFC method Lu-36-T-03) (170 ° C 144 h) -13.7 -10.6 -6.74 variation KV100 after 144 h (ISO 3405) (%) 3.1 4.8 7.1 change in TAN after 144 h (ASTM D664) (mg KOH / g) variation in PAI after 144 h (ASTM D7214) (A.crrl .mm-1) 55 173 102 detergency - overall rating (average) (CEC M-02-A-78) (merit / 10) 6.0 5.4 5.5 elastomer compatibility hardness variation for RE1 fluorocarbon ND 0 0 RE2 polyacrylate ACM ND 1 4 RE3 silastic MCQ ND -22 -21 RE4 nitril HNBR ND 0 1 ND: not available Table 4 Compared to a lubricating composition comprising two Group III oils and one oil Group IV of the state of the art, the lubricant compositions comprising the oil (1) according to the invention have improved properties. The viscosity index is higher or even much higher, and Noack volatility is improved. These parameters therefore make it possible to demonstrate the "fuel-eco" gain of the composition according to the invention. [0043] The lubricant compositions according to the invention also have an oxidation resistance which is greater than that of the lubricant composition of the state of the art. The detergency of the lubricant compositions according to the invention is at the same level or better than that of the lubricant composition of the state of the art. The compatibility of the lubricant compositions according to the invention with the various elastomers that can be used in the transmission joints with which they are in contact is also at the same level or better than that of the lubricant composition of the state of the art. Finally, it can be seen that the improvements in the properties of the lubricating composition comprising 8% of oil (1) according to the invention are of the same order or greater than those of the lubricating composition comprising 27.7% of oil (1) according to the invention. 'invention. EXAMPLE 7 Preparation of a Lubricating Composition According to the Invention, a Comparative Lubricating Composition and Evaluation of the Properties of these Compositions for the Lubrication of a Vehicle Engine Lubricating compositions are prepared by mixing the oil (1) according to Example 1 and known oils with other base oils according to the amounts (`) / 0 by mass) of Table 5. A comparative lubricating composition (3) is also prepared from a comparative oil (2). ) according to the comparative example (3). Composition (5) According to the Invention Comparative Composition (3) Base Oil Group III (KV100 / ASTM D445 = 4.16 mm2s-1) 37.45 37.45 Base Oil Group III: Neste Nexbase 3050 17, 3 17.3 oil (1) according to the invention 27.7 / comparative oil (2) / 27.7 admixture of additives (dispersants, detergent, DTPZn, amino antioxidant, phenolic antioxidant) 10.9 10.9 additive improving viscosity index (PISH) 3.2 3.2 Viscosity index improving additive (PMA) 2.9 2.9 friction reducing additive (MoDTC) 0.5 0.5 anti-corrosion additive Amino type 0.05 0.05 Table 5 The characteristics of the lubricating compositions prepared are evaluated and the results obtained are shown in Table 6. Composition (5) according to the invention Comparative composition (3) kinematic viscosity measured at 100 ° C. ( ASTM D445) (mrr.s-1) 9,672 9,858 Viscosity index (ISO 2909) 202 193 Noack volatility (CEC L-40-93) (%) 9.5 12.3 Dynamic viscosity (CCS) at -35 ° C (AS Table 6 Compared to a lubricating composition comprising two Group III oils and the comparative oil (2) of the state of the art, the lubricating composition comprising the oil (1). ) according to the invention has improved properties. [0044] The kinematic viscosity measured at 100 ° C is lower. The dynamic viscosity (CCS at -35 ° C.) is lower, which puts forward an improvement in the cold behavior of the composition according to the invention. In addition, the viscosity index is much higher and the Noack volatility is greatly improved. These parameters therefore make it possible to demonstrate the "fuel-eco" gain of the composition according to the invention. Example 8: Preparation of a lubricant composition according to the invention, a comparative lubricating composition and evaluation of the properties of these compositions for lubricating a vehicle engine The lubricating compositions are prepared by mixing the oil (1) according to Example 1 and known oils with other base oils and with additives for the preparation of lubricating compositions according to the amounts (% by weight) of Table 7. Composition (6) according to the invention Comparative composition (4) base oil group III (KV100 / ASTM D445 = 4.38 mm2.s-1) 48.7 48.7 base oil group IV PAO (KV100 / ASTM D445 = 4.08 mm2.s-1) 20.0 20.0 oil (1) according to the invention 10.0 / comparative oil (2) / 10.0 admixture of additives (dispersants, detergent, DTPZn, antioxidant amine, phenolic antioxidant) 12.6 12.6 modifier additive friction (glycerol monooleate) 0.5 0.5 pour point improving additive (PMA) 0.2 0.2 additive improving ind Table 7 The characteristics of the lubricating compositions prepared are evaluated and the results obtained are shown in Table 8. Composition (6) according to the invention Comparative composition (4) Viscosity index ( ISO 2909) 195 192 kinematic viscosity measured at 100 ° C (ISO 31404) (mm2.s-1) 8,115 8,043 dynamic viscosity (CCS) at -35 ° C (ASTM D5293) (mPa $) 4,480 4,950 basicity (total base number: TBN) (ASTM D2896) 7.3 7.8 oxidation resistance (Daimler oxidation test FO - DIN 51453) (100 ° C 168 h) (%) -9.1 -13.3 oxidation resistance (Daimler oxidation test 5% B100 - DIN 51453) (100 ° C - 168 h) (%) 18.8 14.2 Fuel Eco (W24 C250 CDI / engine - 0M651 vs MB RL002) (%) 3.84 2.62 Table 8 Compared to a lubricating composition comprising a group III oil, a group IV oil and the comparative oil (2) of the state of the art, the lubricating composition comprising the oil (1 ) according to the inve tion has improved properties, and more particularly in "fuel-eco" gain. The viscosity index is higher. Dynamic viscosity (CCS at -35 ° C) is lower. [0045] Oxidation resistance is improved. EXAMPLE 9 Preparation of a Lubricating Composition According to the Invention, a Comparative Lubricating Composition and Evaluation of the Properties of these Compositions for Lubricating the Transmission of a Motor Vehicle Lubricating compositions are prepared by mixing the oil (2) according to Example 2 and known oils with other base oils and with additives for the preparation of lubricating compositions according to the amounts (% by weight) of Table 9. [0046] Composition (7) according to the invention Comparative composition (5) base oil group IV mPAO (KV100 / ASTM D445 = 3.5 mm2 .s-1) 55 55 oil (2) according to the invention 16.3 / comparative oil (1) / 16.3 viscosity index improver additive (PMA) 6.0 6.0 viscosity index improver additive (PMA) 14.0 14.0 additive mixture (dispersant, detergent, The characteristics of the lubricating compositions prepared are evaluated and the results obtained are shown in Table 10. Composition (7) according to US Pat. Comparative composition (5) Viscosity index (ISO 2909) 212 200 Traction coefficient (MTM: 0.036 0.041 T = 40 ° C, Ve = 1 m / s, SRR = 20% load = 75 N) Table 10 Compared to a lubricating composition comprising a group IV oil and the comparative oil (1) of the state of the art, the lubricating composition comprising the oil (2) according to the present invention. you have improved properties. [0047] The viscosity index is much higher and the tensile coefficient is lowered by more than 12%. These parameters therefore make it possible to demonstrate the "fuel-eco" gain of the composition according to the invention.
权利要求:
Claims (14) [0001] REVENDICATIONS1. Lubricating composition comprising at least one oil of formula (I) OCH3 (I) (I) in which R represents a linear or branched C1-C30-alkyl group; m m and n independently represent an average number ranging from 1 to 5. 10 [0002] 2. Lubricating composition according to claim 1 wherein R represents a group selected from a linear C8-alkyl group; a branched C8-alkyl group; a linear C9-alkyl group; a branched C8-alkyl group; a linear C10-alkyl group; C10-branched alkyl; a linear C11-alkyl group; a C11-branched alkyl group; a linear C12-alkyl group; a C12-branched alkyl group; a linear C13-alkyl group; a C13-branched alkyl group; a linear C14-alkyl group; a branched Clealkyl group; a linear C15-alkyl group; a branched C15-alkyl group. 20 [0003] 3. Lubricating composition according to one of claims 1 or 2 wherein ^ m is greater than or equal to n; or ^ m represents an average number ranging from 2 to 4.5; where n represents an average number ranging from 1.5 to [0004] 4. The lubricating composition according to one of claims 1 to 3 wherein ^ m represents an average number ranging from 2.5 to 3.5; where n represents an average number ranging from 2 to 3. [0005] 5. Lubricating composition according to one of claims 1 to 4 wherein 30 ^ m is an average number of 2.5 and n is an average number of 2; where m represents an average number equal to 3.5 and n represents an average number equal to 2.8. [0006] 6. Lubricating composition according to one of claims 1 to 5 comprising at least one oil of formula (I) of which (a) the kinematic viscosity at 100 ° C, measured according to ASTM D445, is from 2.5 to 4, MrT12.S-1; or (b) the viscosity number is greater than 160 or is between 160 and 210; or (c) the pour point is less than -40 ° C; or (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 1,200 mPa.s. 10 [0007] 7. Lubricating composition according to one of claims 1 to 6 comprising at least one oil of formula (! -) of which (a) the kinematic viscosity at 100 ° C, measured according to ASTM D445, ranges from 2.5 to 4 5 mm 2 S-1; (B) the viscosity number is greater than 160 or is between 160 and 210; (c) the pour point is less than -40 ° C; (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 1200 mPa.s. 20 [0008] 8. Lubricating composition according to one of claims 1 to 7 comprising at least one oil of formula (I) wherein m represents an average number equal to 2.5 and n represents an average number of 2 and (a) the Kinematic viscosity at 100 ° C, measured according to ASTM D445, ranges from 2.5 to 3.5 mm 2 s -1; (B) the viscosity number is between 160 and 180; (c) the pour point is less than -40 ° C; (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 500 mPa.s. 30 [0009] 9. Lubricating composition according to one of claims 1 to 7 comprising at least one oil of formula (I) wherein m represents an average number equal to 3.5 and n represents an average number equal to 2.8 and of which (a) ) the kinematic viscosity at 100 ° C, measured according to ASTM D445, is from 3.5 to 4.5 mm 2 s -1 (b) the viscosity number is from 180 to 210; (c) the pour point is less than -50 ° C (d) the dynamic viscosity (CCS) at -35 ° C, measured according to ASTM D5293 is less than 1200 mPa.s. [0010] 10. Lubricating composition according to one of claims 1 to 9 comprising from 2 to 60% by weight of at least one oil of formula (I), preferably from 2 to 50% by weight of at least one oil of formula (I), more preferably from 5 to 40% by weight of at least one oil of formula (I) and still more preferably from 5 to 30% by weight of at least one oil of formula (I). [0011] 11. Lubricating composition according to one of claims 8 or 10 comprising from 5 to 40% by weight of at least one oil of formula (I), preferably from 10 to 35% by weight of at least one oil of formula (I) and more preferably from 15 to 25% by weight of at least one oil of formula (I). [0012] 12. Lubricating composition according to one of claims 9 or 10 comprising from 5 to 35% by weight of at least one oil of formula (I), preferably from 8 to 30% by weight of at least one oil of formula (I), more preferably 10% by weight, 20% by weight or 30% by weight of at least one oil of formula (I). [0013] The lubricating composition of one of claims 1 to 12 further comprising at least one other base oil selected from Group III oils, Group IV oils and Group V oils; or at least one additive; or at least one other base oil chosen from Group III oils, Group IV oils and Group V oils and at least one additive. [0014] 14, Use of at least one lubricant composition according to one of claims 1 to 13 - for reducing the fuel consumption of an engine, in particular a vehicle engine; or ^ to reduce the fuel consumption of a vehicle equipped with a transmission, in particular a deck or gearbox, lubricated with that compound.3515. Use of at least one lubricant composition according to one of Claims 1 to 13 for reducing the traction coefficient of a transmission oil, in particular of a gearbox oil.
类似技术:
公开号 | 公开日 | 专利标题 EP3174960B1|2021-12-22|Lubricating compositions for motor vehicles EP3274432B1|2021-10-27|Lubricating composition EP2920283B1|2021-07-21|Lubricant composition CA2871433A1|2013-11-07|Lubricant composition for an engine WO2016174186A1|2016-11-03|Ultra-fluid lubricating composition WO2017157979A1|2017-09-21|Polyalkylene glycol-based lubricant composition EP2958980A1|2015-12-30|Lubricating composition based on aminated compounds EP3430110A1|2019-01-23|Polyalkylene glycol-based lubricant composition EP3277738A1|2018-02-07|Star copolymer and use thereof as a viscosity improver EP3237588A1|2017-11-01|Lubricating composition with phase-change material WO2018077780A1|2018-05-03|Lubricant composition WO2017013238A1|2017-01-26|Long duration fuel economy lubricating composition WO2018210829A1|2018-11-22|Use of lubricating compositions to improve the performance of a 4-stroke vehicle engine EP3947610A1|2022-02-09|Use of a lubricant composition for transmission WO2016102528A1|2016-06-30|Lubricating composition comprising a phase-change material WO2021123658A1|2021-06-24|Estolide composition and process for making estolides FR3027915A1|2016-05-06|LUBRICATING COMPOSITIONS COMPRISING A DI-ISOTRIDECYL ADIPATE ALTERNATIVE FR3011246A1|2015-04-03|LUBRICATING COMPOSITION BASED ON COPOLYMERS ETHYLENE / PROPYLENE
同族专利:
公开号 | 公开日 JP2017522428A|2017-08-10| BR112017001845A2|2018-02-27| CN106661478B|2019-09-17| US10202561B2|2019-02-12| CN106661478A|2017-05-10| FR3024461B1|2017-12-29| WO2016016362A1|2016-02-04| US20170226442A1|2017-08-10| MX2017001059A|2017-09-01| CA2955128A1|2016-02-04| JP6695853B2|2020-05-20| EP3174960B1|2021-12-22| EP3174960A1|2017-06-07| KR20170049501A|2017-05-10| MA40199A|2016-02-04|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US20140018273A1|2011-03-29|2014-01-16|Dow Global Technologies Llc|Lubricant compositions| WO2013164449A1|2012-05-04|2013-11-07|Total Marketing Services|Engine lubricant composition| MX221601B|2004-05-14|2004-07-22|Basf Ag|Functional fluids containing alkylene oxide copolymers having low pulmonary toxicity| JP4871606B2|2006-02-03|2012-02-08|出光興産株式会社|Polyether compound and lubricating oil base oil and lubricating oil composition containing the same| WO2009134638A2|2008-04-28|2009-11-05|Dow Global Technologies Inc.|Polyoxyalkylene glycol diether lubricating composition preparation and use| WO2011011656A2|2009-07-23|2011-01-27|Dow Global Technologies Inc.|Polyalkylene glycols useful as lubricant additives for groups i-iv hydrocarbon oils| FR2968011B1|2010-11-26|2014-02-21|Total Raffinage Marketing|LUBRICATING COMPOSITION FOR ENGINE| CN103890154A|2011-11-01|2014-06-25|陶氏环球技术有限责任公司|Oil soluble polyalkylene glycol lubricant compositions| JP6228219B2|2012-10-25|2017-11-08|ダウ グローバル テクノロジーズ エルエルシー|Lubricating composition| JP6422565B2|2014-07-31|2018-11-14|ダウ グローバル テクノロジーズ エルエルシー|Capped oil-soluble polyalkylene glycol with low viscosity and high viscosity index| EP3174964B1|2014-07-31|2020-09-02|Dow Global Technologies Llc|Alkyl capped oil soluble polymer viscosity index improving additives for base oils in automotive applications|US11193083B2|2014-07-31|2021-12-07|Dow Global Technologies Llc|Alkyl capped oil soluble polymer viscosity index improving additives for base oils in industrial lubricant applications| JP6422565B2|2014-07-31|2018-11-14|ダウ グローバル テクノロジーズ エルエルシー|Capped oil-soluble polyalkylene glycol with low viscosity and high viscosity index| RU2711382C2|2014-12-03|2020-01-16|Янссен Фармацевтика Нв|6,7-DIHYDROPYRAZOLO[1,5-A]PYRAZINE-4-ONE COMPOUNDS AND USE THEREOF AS NEGATIVE ALLOSTERIC MODULATORS OF mGluR2 RECEPTORS| CN107429953A|2015-03-30|2017-12-01|开利公司|Low oily refrigerant and steam compression system| FR3048977B1|2016-03-15|2020-02-07|Total Marketing Services|LUBRICATING COMPOSITION BASED ON POLYALKYLENE GLYCOLS| FR3048976B1|2016-03-15|2020-02-07|Total Marketing Services|LUBRICATING COMPOSITION BASED ON POLYALKYLENE GLYCOLS| FR3050996A1|2016-05-04|2017-11-10|Total Marketing Services|HYDRAULIC COMPOSITION LARGE COLD| RU2744972C2|2016-06-02|2021-03-17|Басф Се|Lubricant composition| US10160926B2|2016-11-25|2018-12-25|Hyundai Motor Company|Axle oil composition having enhanced fuel efficiency and low viscosity|
法律状态:
2015-06-25| PLFP| Fee payment|Year of fee payment: 2 | 2016-02-05| PLSC| Publication of the preliminary search report|Effective date: 20160205 | 2016-07-15| PLFP| Fee payment|Year of fee payment: 3 | 2017-08-25| PLFP| Fee payment|Year of fee payment: 4 | 2018-06-21| PLFP| Fee payment|Year of fee payment: 5 | 2020-06-17| PLFP| Fee payment|Year of fee payment: 7 | 2021-06-11| PLFP| Fee payment|Year of fee payment: 8 |
优先权:
[返回顶部]
申请号 | 申请日 | 专利标题 FR1457438A|FR3024461B1|2014-07-31|2014-07-31|LUBRICATING COMPOSITIONS FOR MOTOR VEHICLE|FR1457438A| FR3024461B1|2014-07-31|2014-07-31|LUBRICATING COMPOSITIONS FOR MOTOR VEHICLE| CA2955128A| CA2955128A1|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles| EP15744566.9A| EP3174960B1|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles| KR1020177002745A| KR20170049501A|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles| BR112017001845-4A| BR112017001845A2|2014-07-31|2015-07-30|lubrication composition and uses of at least one lubrication composition| MA040199A| MA40199A|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles| US15/500,265| US10202561B2|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles| CN201580040480.7A| CN106661478B|2014-07-31|2015-07-30|Lubricating composition for motor vehicles| MX2017001059A| MX2017001059A|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles.| PCT/EP2015/067492| WO2016016362A1|2014-07-31|2015-07-30|Lubricating compositions for motor vehicles| JP2017504709A| JP6695853B2|2014-07-31|2015-07-30|Lubricating composition for electric vehicle| 相关专利
Sulfonates, polymers, resist compositions and patterning process
Washing machine
Washing machine
Device for fixture finishing and tension adjusting of membrane
Structure for Equipping Band in a Plane Cathode Ray Tube
Process for preparation of 7 alpha-carboxyl 9, 11-epoxy steroids and intermediates useful therein an
国家/地区
|