FR3118630A1 - Lubricating composition having cold stability and improved fuel eco properties - Google Patents

Abstract

Lubricating composition having cold stability and improved fuel eco properties The invention relates to a lubricating composition comprising at least: - a base oil, - a friction modifier comprising molybdenum, - a borated dispersant, - a polymer comprising repeating units capable of being obtained by polymerization of monomers (a) of formula (I): (I) in which : - R1 represents a hydrogen atom or a methyl group, - - R2 is a polybutylene group, and - P is equal to 0 or 1. Figure for the abstract: None

Description

Lubricating composition having cold stability and improved fuel eco properties

The invention relates to the field of lubricating compositions, in particular the fuel economy properties also designated by the expression fuel economy (FE or fuel eco) and cold stability of the lubricating compositions. The invention relates to the combined use of at least one molybdenum friction modifier, at least one boron dispersant and at least one copolymer of the (meth)acrylate type to improve the properties of fuel economy (FE or fuel eco) and cold stability of a lubricating composition also comprising at least one base oil.

STATE OF THE ART

The needs for high performance lubricating compositions are increasing. In particular, due to increasingly severe conditions of use, for example due to more extreme temperatures or very high mechanical stresses.

The interval between oil changes and the reduction in the size of lubrication systems also lead to an increase in the need for high performance lubricating compositions. Energy efficiency and in particular improving the Fuel Eco (FE) of lubricating compositions or reducing the fuel consumption of engines, in particular vehicle engines, are increasingly important objectives and lead to the use growing number of high performance lubricating compositions.

High performance lubricating compositions must therefore possess improved properties, in particular with regard to kinematic viscosity, viscosity index, volatility, dynamic viscosity or cold pour point.

Thermal stability and resistance to oxidation are also properties to be improved for high performance lubricating compositions.

Engine lubricating compositions must therefore fulfill many objectives.

The lubrication of parts sliding over each other plays a decisive role, in particular to reduce friction and wear, allowing fuel savings in particular.

An essential requirement of engine lubricating compositions relates to environmental aspects. It has in fact become essential to reduce the consumption of lubricating compositions as well as fuel consumption, in particular with the aim of reducing CO ₂ emissions.

The nature of automotive engine lubricating compositions has an influence on fuel consumption. Engine lubricating compositions for automobiles that allow energy savings are often referred to as fuel eco (FE), in English terminology.

The reduction of energy losses is therefore a constant research in the field of automotive lubricating compositions.

There is therefore a need to have available lubricating compositions for engines, in particular for vehicle engines, which make it possible to provide a solution to all or part of the problems of the lubricating compositions of the state of the art, in particular as regards the cold stability of the lubricating composition as well as the fuel eco properties obtained thanks to a low coefficient of friction.

The invention relates first of all to a lubricating composition comprising:

- at least one base oil,

- at least one friction modifier comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 100 ppm to 1500 ppm by weight, relative to the total weight of the lubricating composition,

- at least one boron dispersant, such that the amount of boron element in the lubricating composition ranges from 10 ppm to 300 ppm, relative to the total weight of the lubricating composition,

- from 0.1% to 10% by weight of dry matter, relative to the total weight of the lubricating composition, of a polymer comprising repeating units capable of being obtained by polymerization of monomers (a) of formula (I) :

(I)

in which :

- R1 represents a hydrogen atom or a methyl group,

- X1 represents a group chosen from: -O-, -O(AO)m, or –NH-, each group A independently representing a C2-C4 alkylene group and m an integer ranging from 0 to 10,

- R2 is a polybutylene group, and

- P is equal to 0 or 1.

According to one embodiment, the lubricating composition according to the invention comprises:

- at least 50% by weight, relative to the total weight of the lubricating composition, of one or more base oils,

- from 0.01% to 10% by weight, relative to the total weight of the lubricating composition, of one or more friction modifiers comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 300 ppm at 1000 ppm by weight, relative to the total weight of the lubricating composition,

- from 0.01% to 10% by weight, relative to the total weight of the lubricating composition, of one or more boron dispersants, such that the amount of boron element in the lubricating composition ranges from 10 ppm to 300 ppm in weight, relative to the total weight of the lubricating composition,

- from 0.5% to 5% by weight of dry matter, relative to the total weight of the lubricating composition, of a copolymer obtainable by copolymerization of monomers (a) of formula (I) and monomers ( b) of formula (II):

(II)

in which :

- R3 represents a hydrogen atom or a methyl group,

- X2 represents an -O- or -NH- group,

- the R4 groups represent, independently, a C2-C4 alkylene group,

- R5 represents a C1-C8 alkyl group, and

- Q is an integer ranging from 1 to 20.

Advantageously, the lubricating composition according to the invention comprises:

- at least 70% by weight, relative to the total weight of the lubricating composition, of one or more base oils,

- from 0.01% to 5% by weight, relative to the total weight of the lubricating composition, of one or more friction modifiers comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 500 ppm at 1000 ppm by weight, relative to the total weight of the lubricating composition,

- from 0.01% to 5% by weight, relative to the total weight of the lubricating composition, of one or more boron dispersants, such that the amount of boron element in the lubricating composition ranges from 20 ppm to 300 ppm in weight, relative to the total weight of the lubricating composition,

- from 0.8% to 3% by weight of dry matter, relative to the total weight of the lubricating composition, of a copolymer comprising, relative to the total weight of the copolymer:

- from 1% to 50% by weight of units derived from monomers (a), and

- from 1% to 80% by weight of units derived from monomers (b).

Preferably, the lubricating composition according to the invention has a kinematic viscosity at 100° C., measured according to the ASTM D445 standard, ranging from 3.8 mm²/s to 21.9 mm²/s.

Preferably, the friction modifier comprising molybdenum is an organomolybdenum compound, in particular a compound chosen from a molybdenum dithiocarbamate derivative (MoDTC), a molybdenum dithiophosphate derivative (MoDTP) or a sulfur-free molybdenum complex, preferably a derivative molybdenum dithiocarbamate (MoDTC).

Preferably, the borated dispersant is chosen from borated succinimides, preferably from borated polyisobutene succinimides.

A subject of the invention is also the use, in a lubricating composition comprising a base oil, one or more molybdenum friction modifiers and one or more boron dispersants, of a copolymer comprising repeating units capable of being obtained by polymerization of monomers (a) of formula (I):

(I)

in which :

- R1 represents a hydrogen atom or a methyl group,

- X1 represents a group chosen from: -O-, -O(AO)m, or –NH-, each group A independently representing a C2-C4 alkylene group and m an integer ranging from 0 to 10,

- R2 is a polybutylene group, and

- P is equal to 0 or 1,

to improve the cold stability of said lubricating composition.

Preferably, the use of the copolymer according to the invention makes it possible to:

- lubricate the parts of a motor vehicle engine, and/or

- reduce friction between engine parts, and/or

- reduce engine fuel consumption.

DETAILED DESCRIPTION

The present invention relates firstly to a lubricating composition comprising:

- at least one base oil,

- at least one friction modifier comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 100 ppm to 1500 ppm by weight, relative to the total weight of the lubricating composition,

- at least one boron dispersant, such that the amount of boron element in the lubricating composition is from 10 ppm to 300 ppm, relative to the total weight of the lubricating composition,

- from 0.1 to 10% by weight of dry matter, relative to the total weight of the lubricating composition, of a polymer comprising repeating units capable of being obtained by polymerization of monomers (a) of formula (I):

(I)

in which :

• R ¹ represents a hydrogen atom or a methyl group,
• X ¹ represents a group chosen from: -O-, -O(AO) _m , or –NH-, each group A independently representing a C2-C4 alkylene group and m an integer ranging from 0 to 10,
• R ² is a polybutylene group, and
• P is equal to 0 or 1.

VS copolymer

The lubricating composition according to the invention comprises at least one polymer, in particular a copolymer, comprising repeating units capable of being obtained by polymerization of monomers (a) of formula (I):

(I)

in which :

• R ¹ represents a hydrogen atom or a methyl group,
• X ¹ represents a group chosen from: -O-, -O(AO) _m , or –NH-, each group A independently representing a C ₂ -C ₄ alkylene group and m an integer ranging from 0 to 10 ,
• R ² is a polybutylene group, and
• P is equal to 0 or 1.

Within the meaning of the present invention, the term “(meth)acrylate” designates a methacrylate or an acrylate. By analogy, within the meaning of the present invention, the term “(meth)acrylamide” designates a methacrylamide or an acrylamide.

Preferably, R ¹ is a methyl group.

Among the examples of a C ₂ -C ₄ alkylene group, mention may in particular be made of an ethylene group, a 1,2- or 1,3-propylene group or else a 1,2, 1,3- or 1,4- butylene.

Preferably, m is an integer ranging from 0 to 4, more preferably from 0 to 2.

In the case where m is greater than or equal to 2, each A can be the same or different, and the fragments (AO) _m can be linked randomly or in blocks.

Preferably, the group X ¹ is a group -O- or -O(AO) _m -, more preferably a group -O- or -O(CH ₂ CH ₂ O)-.

R ² is a polybutylene group.

By "polybutylene group" is meant within the meaning of the invention a group obtained by the elimination of a hydrogen atom from a hydrocarbon polymer containing, as essential structural unit, at least one type 1 monomer, 2 butylene or isobutylene.

As an example of a hydrocarbon polymer suitable for the preparation of a polybutylene group R ² , mention may in particular be made of a copolymer comprising units derived from isobutene and/or 1,2-butylene or even a polymer obtained by hydrogenation of the terminal double bond of a polybutadiene obtained by the 1,2 addition of buta-1,3-diene monomers.

The hydrocarbon polymer can be a block polymer or a random polymer.

The hydrocarbon-based polymer may also contain at least one structural unit distinct from the isobutylene or 1,2-butylene units.

The hydrocarbon polymer may for example comprise one or more of the following units:

(1) unsaturated aliphatic hydrocarbons,

(2) alicyclic unsaturated hydrocarbons, and

(3) unsaturated hydrocarbons containing an aromatic group,

other than the isobutene, but-1-ene and but-2-ene units.

If the hydrocarbon polymer has a double bond, this double bond can be partially or totally hydrogenated by hydrogenation.

Preferably, the isobutylene and 1,2-butylene units represent at least 30% in moles of the total number of structural units constituting the hydrocarbon polymer, preferably at least 40% in moles, preferably at least 50% in moles , preferably at least 60 mol%.

The total number of butylene units (isobutylene and/or 1,2 butylene), relative to the total number of structural units of the hydrocarbon polymer, can be determined by analyzing the hydrocarbon polymer by ¹³ C nuclear magnetic resonance spectroscopy and using the following equation:

The ¹³ C nuclear magnetic resonance spectrum shows a peak derived from an isobutylene methyl group at 30-32 ppm (integral value A), and a peak derived from a branched methylene group (-CH ₂ -CH(CH ₂ CH ₃ )-) of 1,2-butylene at 26-27 ppm in integral value (integral value B). The total number of isobutylene and 1,2-butylene can be determined from the integral values of the peaks and an integral value (integral value C) of the peaks of all the carbon atoms of the hydrocarbon polymer.

The monomers (a) are typically obtained by esterification or amidation of a (co)polymer (Y) containing a hydroxyl group or an amine group.

Among the examples of (co)polymers (Y) (that is to say the (co)polymer containing a hydroxyl group or an amine group), mention may be made by way of examples of the (co)polymers (Y1) to (Y4) containing a hydroxyl group and the (co)polymers (Y5) containing an amine group as defined below.

The products of addition of alkylene oxide (Y1): (co)polymers capable of being obtained by bringing an alkylene oxide into contact, for example ethylene oxide or propylene oxide, with a polymer selected from: (1) a hydrocarbon polymer obtained by the polymerization of an unsaturated aliphatic hydrocarbon; (2) an unsaturated alicyclic hydrocarbon; (3) an unsaturated aromatic hydrocarbon, chosen in particular from C ₂ -C ₃₆ olefins; and their derivatives, in the presence of an ionic polymerization catalyst, for example a sodium catalyst.

THE pr produced s got s by hydroboration (Y2): (co)polymer obtainable by the hydroboration of hydrocarbon polymers, in particular that described in US 4,316,973.

Adducts of the maleic anhydride-ene-amine alcohol (Y3) type: (co)polymers capable of being obtained by imidation of the product obtained by an Alder-ene reaction between a hydrocarbon polymer having a double bond and the anhydride maleic acid, in the presence of an amino alcohol.

Products capable of being obtained by hydroformylation and hydrogenation (Y4): (co)polymer(s) capable of being obtained by hydroformylation of a hydrocarbon polymer having a double bond, followed by a hydrogenation step. Mention may be made, by way of example, of the products described in JP-A 63-175096.

Maleic anhydride-ene-ethylenediamine (Y5) adducts: (co)polymers capable of being obtained by imidation of a product obtained by an Alder-ene reaction between a hydrocarbon polymer having a double bond and the anhydride maleic, in the presence of ethylenediamine.

Preferably, the (co)polymer (Y) is chosen from (co)polymers (Y1), (Y2) and (Y3), more preferably from (co)polymers (Y) and (Y1).

The number-average molecular weight (Mn) of each of the (co)polymers (Y) is preferably from 1,000 to 25,000 g.mol ^-1 , more preferably from 2,000 to 20,000 g.mol ^-1 , particularly preferably from 3,000 to 15,000 g.mol ^-1 , more preferably from 4,000 to 10,000 g.mol ^-1 .

Advantageously, the crystallization temperature of the (co)polymer (Y) is less than or equal to -40° C., more preferably less than or equal to -50° C., in particular less than or equal to -55° C., typically less than or equal to -60 °C.

The crystallization temperature of the (co)polymer (Y) or of the (co)polymer (A) can be measured using a differential scanning calorimeter of the "Unix® DSC7" type (PerkinElmer). The crystallization temperature is measured during isothermal cooling of a sample (5 mg) of (co)polymer (Y) or (co)polymer (A) from 100°C to -80°C at a rate of 10 ° C/min.

According to one embodiment, the copolymer also comprises repeating units capable of being obtained by the polymerization of monomers (b) of formula (II):

(II)

in which :

- R ³ is a hydrogen atom or a methyl group;

- X ² is a group represented by -O- or -NH-;

- the R ⁴ groups represent, independently, a C ₂ -C ₄ alkylene group;

- R ⁵ is a C ₁ -C ₈ alkyl group; And

- q is an integer ranging from 1 to 20.

Preferably, R ³ is a methyl group.

Preferably, X ² is an -O- group.

As examples of C ₂ -C ₄ alkylene groups, mention may in particular be made of ethylene, isopropylene, 1,2- or 1,3-propylene, isobutylene and 1,2-, 1 ,3- or 1,4-butylene.

Preferably, q is equal to 1 or 2.

When q is equal to or greater than 2, each R ⁴ can be the same or different, and the fragments (R ⁴ O)q can be linked randomly or in blocks.

As examples of C ₁ -C ₈ alkyl groups, mention may in particular be made of methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, t-butyl, n-heptyl, isoheptyl, n-hexyl , 2-ethylhexyl, n-pentyl and n-octyl.

Among these C ₁ -C ₈ alkyl groups, preference will be given to C ₁ -C ₆ alkyl groups, more preferably C ₁ -C ₅ alkyl groups, typically C ₄ alkyl groups.

Examples of monomers (b) include methoxypropyl (meth)acrylate, methoxybutyl (meth)acrylate, methoxyheptyl (meth)acrylate, methoxyhexyl (meth)acrylate, methoxybutyl (meth)acrylate, methoxypentyl, methoxyoctyl (meth)acrylate, ethoxyethyl (meth)acrylate, ethoxypropyl (meth)acrylate, ethoxybutyl (meth)acrylate, ethoxyheptyl (meth)acrylate, ethoxyhexyl (meth)acrylate , ethoxypentyl (meth)acrylate, ethoxyoctyl (meth)acrylate, propoxymethyl (meth)acrylate, propoxyethyl (meth)acrylate, propoxypropyl (meth)acrylate, propoxybutyl (meth)acrylate, propoxyheptyl, propoxyhexyl (meth)acrylate, propoxypentyl (meth)acrylate, propoxyoctyl (meth)acrylate, butoxymethyl (meth)acrylate, butoxyethyl (meth)acrylate, butoxypropyl (meth)acrylate, butoxybutyl (meth)acrylate , butoxyheptyl (meth)acrylate, butoxyhexyl (meth)acrylate, butoxypentyl (meth)acrylate, Butoxyoctyl (meth)acrylate and esters of (meth)acrylic acid and C ₁ -C ₈ alcohols with 2 to 20 moles of ethylene oxide, propylene oxide or butylene oxide.

Advantageously, the monomers (b) are chosen from ethoxyethyl (meth)acrylate and butoxyethyl (meth)acrylate.

According to a preferred embodiment, the monomers (b) are distinct from the monomers (a).

According to one embodiment, the copolymer of the invention may also comprise, in addition to the units derived from the monomers (a) and (b), additional repeating units capable of being obtained by the polymerization of monomers chosen from:

- the monomers (c) chosen from C ₁ -C 4 alkyl (meth)acrylates,

- the monomers (d) chosen from alkyl (meth)acrylates in which the alkyl group is chosen from linear C ₁₂ -C ₃₆ alkyl groups, and/or

- the monomers (e) chosen from alkyl (meth)acrylates in which the alkyl group is chosen from branched C ₁₂ -C ₃₆ alkyl groups.

As examples of monomers (c), mention may in particular be made of: methyl (meth)acrylate, ethyl (meth)acrylate, propyl (meth)acrylate and butyl (meth)acrylate.

Preferably, the monomers (C) are chosen from methyl (meth)acrylate and butyl (meth)acrylate, more preferably from butyl (meth)acrylates.

As examples of monomers (d), mention may in particular be made of: n-dodecyl (meth)acrylate, n-tridecyl (meth)acrylate, n-tetradecyl (meth)acrylate, (meth) n-pentadecyl acrylate, n-hexadecyl (meth)acrylate, n-octadecyl (meth)acrylate, n-icosyl (meth)acrylate, n-tetracosyl (meth)acrylate, n-triacontyl (meth)acrylate and n-hexatriacontyl (meth)acrylate.

Preferably, the monomers (d) are chosen from alkyl (meth)acrylates having a linear C ₁₂ -C ₂₈ alkyl group, more preferably from alkyl (meth)acrylates having a linear C ₁₂ alkyl group -C ₂₂ .

The (co)polymer of the invention may also contain repeating units capable of being obtained by the polymerization of monomers (e) represented by the following formula (III):

(III)

in which :

- R ⁶ is a hydrogen atom or a methyl group;

- X ³ is an -O- or -NH- group;

- the R ⁷ groups represent, independently, a C ₂ -C ₄ alkylene group;

-R⁸ and R⁹independently represent a linear C-alkyl group₄-VS₂₄; And

- r is an integer ranging from 0 to 20.

Preferably, R ⁶ is a methyl group.

Preferably, X ³ is an –O- group.

As examples of C ₂ -C ₄ alkylene groups, mention may in particular be made of ethylene, isopropylene, 1,2- or 1,3-propylene, isobutylene and 1,2-, 1,3- or 1,4-butylene.

Preferably, r is an integer ranging from 0 to 5, more preferably from 0 to 2.

When r is greater than or equal to 2, the R ⁷ groups can be identical or different, and the (R ⁷ O)r fragments can be linked randomly or in blocks.

As examples of linear C ₄ -C ₂₄ alkyl groups, mention may in particular be made of n-butyl, n-heptyl, n-hexyl, n-pentyl, n-octyl, n-nonyl, n-decyl, n-undecyl, n-dodecyl, n-tetradecyl, n-hexadecyl, n-octadecyl, n-eicosyl and n-tetracosyl.

Preferably, the R ⁸ and R ⁹ groups are chosen, independently, from linear C ₆ -C ₂₄ alkyl groups, more preferably from linear C 6 -C ₂₀ alkyl groups, typically from linear C ₆ -C 20 alkyl groups. _C8 - _C16 .

As examples of monomers (e), mention may in particular be made of: 2-octyldecyl (meth)acrylate, an ester of ethylene glycol mono-2-octylpentadecyl ether and (meth)acrylic acid, ( 2-octyldodecyl meth)acrylate, 2-n-decyltetradecyl (meth)acrylate, 2-n-dodecylhexadecyl (meth)acrylate, 2-tetradecyloctadecyl (meth)acrylate, 2-dodecylpentadecyl (meth)acrylate , 2-tetradecylheptadecyl (meth)acrylate, 2-hexadecylheptadecyl (meth)acrylate, 2-heptadecylicosyl (meth)acrylate, 2-hexadecyldocosyl (meth)acrylate, 2-eicosyldocosyl (meth)acrylate, (meth)acrylate 2-tetracosylhexacosyl and N-2-octyldecyl (meth)acrylamide.

Preferably, the monomers (e) are chosen from alkyl (meth)acrylates in which the alkyl group is chosen from branched C ₁₂ -C ₃₆ alkyl groups, more preferably C ₁₄ -C ₃₂ , typically C ₁₆ - _C28 .

Monomers (b) to (e) are obtained by reacting a terminal hydroxyl group or an amine group of a compound comprising a hydrocarbon group with a (meth)acrylic acid, but not by modifying a hydrocarbon polymer. Thus, monomers (b) through (e) are not polyolefin-based monomers. In addition, those obtained by adding 2 to 20 moles of ethylene oxide, propylene oxide or butylene oxide to C ₁ -C ₈ alcohols and those obtained by adding 1 to 20 moles of ethylene oxide, propylene oxide or butylene oxide to alcohols containing branched C ₁₀ -C ₅₀ alkyl groups are also not obtained by modification of hydrocarbon-based polymers. Thus, these monomers are not polyolefin-based monomers.

According to one embodiment, the (co)polymer of the invention comprises, in addition to the units derived from monomers (a) to (e), repeating units obtained by polymerization of monomers chosen from the group consisting of:

- (f) monomers containing nitrogen,

- (g) monomers containing a hydroxyl group, and

- (h) monomers containing phosphorus (h).

Among the examples of monomer (f), mention may be made of the following monomers (f1) to (f4):

Examples of monomers (f1): (meth)acrylamides; monoalkyl(meth)acrylamides, in particular those in which a C1-C4 alkyl group is linked to a nitrogen atom, such as for example N-methyl(meth)acrylamide, N-ethyl(meth)acrylamide, N- isopropyl(meth)acrylamide, N-n-butyl(meth)acrylamide and N-isobutyl(meth)acrylamide]; N-(N′-monoalkylaminoalkyl)(meth)acrylamides, in particular those in which a C2-C6 aminoalkyl group in which a C1-C4 alkyl group is bonded to a nitrogen atom, such as for example N-(N ′-methylaminoethyl)(meth)acrylamide, N-(N′-ethylaminoethyl)(meth)acrylamide, N-(N′-isopropylamino-n-butyl)(meth)acrylamide, N-(N′-n- butylamino-n-butyl)(meth)acrylamide, and N-(N′-isobutylamino-n-butyl)(meth)acrylamide; dialkyl(meth)acrylamides; in particular those in which two C1-C4 alkyl groups are bonded to a nitrogen atom, such as for example N,N-dimethyl(meth)acrylamide, N,N-diethyl(meth)acrylamide, N,N-diisopropyl (meth)acrylamide and N,N-di-n-butyl(meth)acrylamide; N-(N′,N′-dialkylaminoalkyl)(meth)acrylamides, in particular those comprising a C2-C6 aminoalkyl group in which two C1-C4 alkyl groups are linked to a nitrogen atom of an aminoalkyl group such as for example N-(N′,N′-dimethylaminoethyl)(meth)acrylamide, N-(N′,N′-diethylaminoethyl)(meth)acrylamide, N-(N′,N′-dimethylaminopropyl)(meth )acrylamide, and N-(N′,N′-di-n-butylaminobutyl)(meth)acrylamide; N-vinylcarboxylic acid amides such as for example N-vinylformamide, N-vinylacetamide, N-vinyl-n-isopropionic acid amide, N-vinyl-isopropionic acid amide and N- vinylhydroxyacetamide.

Example of monomer (f2): 4-nitrostyrene.

Examples of monomers (f3):

- monomers containing primary amine groups: C3-C6 alkenylamines, such as for example (meth)allylamine and crotylamine; C2-C6 aminoalkyl (meth)acrylates, such as, for example, aminoethyl (meth)acrylate;

- monomers containing secondary amine groups: monoalkylaminoalkyl (meth)acrylates, in particular those comprising a C2-C6 aminoalkyl group in which a C1-C6 alkyl group is bonded to a nitrogen atom, such as ( N-t-butylaminoethyl meth)acrylate and N-methylaminoethyl (meth)acrylate; C6-C12 dialkenylamines, for example di(meth)allylamine;

- monomers containing tertiary amine groups: dialkylaminoalkyl (meth)acrylates, in particular those comprising a C2-C6 aminoalkyl group in which two C1-C6 alkyl groups are bonded to a nitrogen atom, such as ( N,N-dimethylaminoethyl meth)acrylate and N,N-diethylaminoethyl (meth)acrylate; alicyclic (meth)acrylates comprising a nitrogen atom such as, for example, morpholinoethyl (meth)acrylate; aromatic monomers such as for example N-(N′,N′-diphenylaminoethyl)(meth)acrylamide, N,N-dimethylaminostyrene, 4-vinylpyridine, 2-vinylpyridine, N-vinylpyrrole, N-vinylpyrrolidone and N-vinylthiopyrrolidone], and

- hydrochlorides, sulfates, phosphates and lower alkyl monocarboxylates (C1-C8) of these monomers, acetic acid and propionic acid being examples of monocarboxylic acids.

Example of a monomer containing a nitrile group (f4): (meth)acrylonitrile.

Preferably, the monomers (f) are chosen from monomers (f1) and (f3), more preferably from N-(N′,N′-diphenylaminoethyl)(meth)acrylamide, N-(N′,N′ -dimethylaminoethyl)(meth)acrylamide, N-(N′,N′-diethylaminoethyl)(meth)acrylamide, N-(N′,N′-dimethylaminopropyl)(meth)acrylamide, N (meth)acrylate, N-dimethylaminoethyl and N,N-diethylaminoethyl (meth)acrylate.

By way of examples of monomers (g), mention may in particular be made of:

- aromatic monomers containing a hydroxyl group, such as p-hydroxystyrene; C2-C6 hydroxyalkyl (meth)acrylates such as, for example, 2-hydroxyethyl (meth)acrylate and 2- or 3-hydroxypropyl (meth)acrylate; substituted C1-C4 mono- or bis-hydroxyalkyl (meth)acrylamides such as, for example, N,N-bis(hydroxymethyl)(meth)acrylamide, N,N-bis(hydroxypropyl)(meth)acrylamide and N, N-bis(2-hydroxybutyl)(meth)acrylamide; vinyl alcohol; C3-C12 alkenols such as (meth)allylic alcohol, crotyl alcohol, isocrotyl alcohol, 1-octenol and 1-undecenol; monools or diols of C4-C12 alkenes such as for example 1-butene-3-ol, 2-butene-1-ol and 2-butene-1,4-diol; hydroxyalkyl C1-C6 alkenyl C3-C10 ethers such as 2-hydroxyethylpropenyl ether; C3-C10 alkenyl ethers or (meth)acrylates of polyhydric alcohols comprising from 3 to 8 hydroxyl groups (in particular chosen from among glycerol, pentaerythritol, sorbitol, sorbitan, diglycerol, sugars and sucrose ) such as the (meth)allylic ether of sucrose.

- polyoxyalkylene glycols in which the alkylene group is C2-C4 and the degree of polymerization is from 2 to 50; polyoxyalkylene polyols such as, for example, polyoxyalkylene ethers of polyhydric alcohols comprising from 3 to 8 hydroxyl groups, the alkylene group being C2-C4, and the degree of polymerization ranging from 2 to 100; mono(meth)acrylates of C1-C4 alkyl ethers of polyoxyalkylene glycols or of polyoxyalkylene polyols such as for example polyethylene glycol (Mn from 100 to 300 g.mol ^-1 ), polypropylene glycol mono(meth)acrylate (Mn: from 130 to 500 g.mol ^-1 ), methoxy polyethylene glycol mono(meth)acrylate (Mn: from 110 to 310 g.mol ^-1 ), the product of the addition of lauryl alcohol with oxide of ethylene (2 to 30 moles), and polyoxyethylene mono(meth)acrylate (Mn: from 150 to 230 g.mol ⁻¹ ) sorbitan.

The monomers (h) are chosen in particular from the following monomers (h1) and (h2).

Examples of monomers (h1): (meth)acryloyloxyalkyl C2-C4 phosphate esters such as for example (meth)acryloyloxyethyl phosphate and (meth)acryloyloxyisopropyl phosphate; alkenyl phosphate esters such as for example vinyl phosphate, allyl phosphate, propenyl phosphate, isopropenyl phosphate, butenyl phosphate, pentenyl phosphate, octenyl phosphate, phosphate decenyl and dodecenyl phosphate. The term "(meth)acryloyloxy" means acryloyloxy or methacryloyloxy.

Examples of monomers (h2): (meth)acryloyloxy alkyl C2-C4 phosphonic acids such as for example (meth)acryloyloxyethyl phosphonic acid; alkenyl C2-C12 phosphonic acids such as vinylphosphonic acid, allylphosphonic acid and octenylphosphonic acid.

Preferably, the monomers (h) are chosen from monomers (h1), more preferably from (meth)acryloyloxyalkyl C2-C4 phosphate esters, advantageously the monomers (h) are (meth)acryloyloxyethyl phosphate.

According to one embodiment, the (co)polymer of the invention comprises, in addition to the units derived from monomers (a) to (h), repeating units obtained by polymerization of monomers (i) comprising at least two unsaturated groups.

Among the examples of monomer (i), mention may be made of divinylbenzene; C4-C12 alkadienes such as butadiene, isoprene, 1,4-pentadiene, 1,6-heptadiene and 1,7-octadiene; (di)cyclopentadiene; vinylcyclohexene and ethylidene-bicycloheptene, limonene, ethylene di(meth)acrylate, polyalkylene oxide glycol di(meth)acrylate, pentaerythritol triallyl ether, trimethylolpropane tri(meth)acrylate, and esters disclosed in WO 01/009242 such as for example a glycolic ester of an unsaturated carboxylic acid having a number average molecular mass (Mn) greater than or equal to 500 g.mol ^-1 or an ester of an unsaturated alcohol and of a carboxylic acid.

The (co)polymer of the invention may also comprise, in addition to the units derived from monomers (a) to (i), repeating units obtained by polymerization of monomers chosen from:

- (j) monomers based on aliphatic hydrocarbons,

- (k) monomers based on alicyclic hydrocarbons,

- (l) hydrocarbon-based aromatic monomers,

- (m) monomers of vinyl esters, vinyl ethers and vinyl ketones,

- (n) monomers containing an epoxy group,

- (o) monomers containing a halogen,

-(p) unsaturated polycarboxylic acid ester type monomers.

Examples of monomer (j): C ₂ -C ₂₀ alkenes such as for example ethylene, propylene, butene, isobutylene, pentene, heptene, diisobutylene, octene, dodecene and octadecene.

Examples of monomer (k): cyclopentene, cyclohexene, cycloheptene, cyclooctene and pinene.

Examples of monomers (l): styrene, α-methylstyrene, vinyltoluene, 2,4-dimethylstyrene, 4-ethylstyrene, 4-isopropylstyrene, 4-butylstyrene, 4-phenylstyrene, 4-cyclohexylstyrene , 4-benzylstyrene, 4-crotylbenzene, indene and 2-vinylnaphthalene.

Examples of monomers (m): vinyl esters of saturated C2-C12 fatty acids such as for example vinyl acetate, vinyl propionate, vinyl butyrate and vinyl octanoate; C1-C12 alkyl, aryl or alkoxyalkylvinyl ethers (methyl vinyl ether, ethyl vinyl ether, propyl vinyl ether, butyl vinyl ether; 2-ethylhexyl vinyl ether; phenyl vinyl ether; vinyl-2-methoxyethyl ether; and vinyl-2-butoxyethyl ether); and C1-C8 alkyl or aryl vinyl ketones (such as for example methyl vinyl ketone, ethyl vinyl ketone, and phenyl vinyl ketone).

Examples of monomers containing an epoxy group (n): glycidyl (meth)acrylate and glycidyl (meth)allyl ether.

Examples of monomers containing a halogen (o): vinyl chloride, vinyl bromide, vinylidene chloride, (meth)allyl chloride and halogenated styrenes such as for example dichlorostyrene.

Examples of unsaturated polycarboxylic acid ester monomers (p): alkyl, cycloalkyl or aralkyl esters of unsaturated polycarboxylic acids [C1-C8 alkyl diesters (dimethyl maleate, dimethyl fumarate, diethyl maleate and maleate dioctyl) of unsaturated dicarboxylic acids (such as maleic acid, fumaric acid and itaconic acid)].

The composition of the copolymer can be determined by proton nuclear magnetic resonance spectroscopy (NMR¹H) or by gas chromatography coupled with mass spectrometry (GC-MS).

Preferably, the monomers (a) represent from 1% to 50% by weight, relative to the total weight of the (co)polymer, more preferably from 5% to 40% by weight, in particular from 8% to 40% by weight, typically 10% to 30% by weight.

Preferably, the monomers (b) represent from 1% to 80% by weight, relative to the total weight of the (co)polymer, more preferably from 5% to 60% by weight, in particular from 10% to 35% by weight, typically 10% to 30% by weight.

Preferably, the monomers (a) and (b) together represent at least 10% by weight of the total weight of the (co)polymer, more preferably from 15% to 90% by weight, in particular from 20% to 80% by weight, typically 20% to 50% by weight.

Preferably, the monomers (c) represent from 1% to 80% by weight, relative to the total weight of the (co)polymer, more preferably from 20% to 70% by weight, in particular from 30% to 65% by weight.

Preferably, the monomers (d) represent from 1% to 40% by weight, relative to the total weight of the (co)polymer, more preferably from 1% to 35% by weight, in particular from 2% to 30% by weight.

Preferably, the monomers (e) represent from 0% to 40% by weight, relative to the total weight of the (co)polymer, more preferably from 1% to 30% by weight, in particular from 1% to 25% by weight.

Preferably, the monomers (f), (h) and (h) each represent from 0% to 15% by weight, relative to the total weight of the (co)polymer, more preferably from 1% to 12% by weight, in particular from 2% to 10% by weight.

Preferably, the monomers (i) represent from 0.01 ppm to 200 ppm by weight, relative to the total weight of the (co)polymer, more preferably from 0.005 ppm to 50 ppm by weight, in particular from 0.1 ppm to 20 ppm by weight.

Preferably, the monomers (j) to (p) each represent from 0 ppm to 10% by weight, relative to the total weight of the (co)polymer, more preferably from 1% to 7% by weight, in particular from 2% to 5% by weight.

Preferably, the copolymer has a mass-average molecular weight (Mw) of 5,000 g.mol ^-1 to 2,000,000 g.mol ^-1 , more preferably of 150,000 g.mol ^-1 to 1,000,0000 g.mol ^-1 , in particular from 230,000 g.mol ^- 1 to 1,000,000 g.mol ^-1 , in particular from 300,000 g.mol ^-1 to 800,000 g.mol ^-1 . The weight average molar mass can be determined by steric exclusion chromatography with poly(methyl methacrylate) (PMMA) standards.

The (co)polymer preferably has a crystallization temperature of less than or equal to -30°C, more preferably less than or equal to -40°C, in particular less than or equal to -50°C, typically less than or equal to -60 °C.

The copolymer implemented according to the invention can be synthesized according to any method well known to those skilled in the art or can be found commercially.

Specific examples include a method in which the monomers are subjected to solution polymerization in a solvent in the presence of a polymerization catalyst.

Examples of solvent include toluene, xylene, C9-C10 alkylbenzenes, methyl ethyl ketone and mineral oils.

Examples of polymerization catalysts: azo catalysts (such as 2,2′-azobis(2-methylbutyronitrile) and 2,2′-azobis(2,4-dimethylvaleronitrile)), peroxide catalysts (such as benzoyl peroxide, cumyl peroxide and lauryl peroxide) and redox catalysts (such as mixtures of benzoyl peroxide and tertiary amines). If necessary, a known chain transfer agent (such as C2-C20 alkyl mercaptans) can also be used.

The polymerization temperature is preferably 25°C to 140°C, more preferably 50°C to 120°C.

The (co)polymer of the invention can also be obtained by bulk, emulsion or suspension polymerization

When the (co)polymer is a copolymer, it can be one of the following types: a random addition polymer, an alternative copolymer, a graft copolymer and a block copolymer.

The copolymer of the invention is used in the lubricating composition, preferably in an amount ranging from 0.1% to 10% by weight of dry matter, more preferably from 0.5% to 5% by weight of dry matter. dry, even more preferably from 0.8% to 3% by weight of dry matter, relative to the total weight of the lubricating composition.

Molybdenum Friction Modifier

The lubricating composition according to the invention comprises one or more friction modifiers comprising molybdenum, such that the amount of molybdenum in the lubricating composition ranges from 100 ppm to 1500 ppm by weight, preferably from 300 ppm to 1000 ppm by weight, more preferably from 500 ppm to 1000 ppm by weight, relative to the total weight of the lubricating composition.

The quantity of molybdenum element, in particular of MoDTC compounds, of the lubricating composition according to the invention can be measured according to standard ASTM D5185.

According to one embodiment, the lubricating composition comprises from 0.01% to 10% by weight, preferably from 0.1% to 5% by weight, more preferably from 0.5% to 3% by weight, of modifier (s) molybdenum friction, based on the total weight of the lubricating composition.

Preferably, the friction modifier(s) comprising molybdenum are chosen from organomolybdenum compounds, in particular chosen from molybdenum dithiocarbamate derivatives (MoDTC), molybdenum dithiophosphate derivatives (MoDTP) or sulfur-free molybdenum complexes, preferably still among molybdenum dithiocarbamate derivatives (MoDTC).

Molybdenum dithiocarbamate compounds (MoDTC compound) are complexes formed from a metal nucleus bonded to one or more ligands independently chosen from alkyl dithiocarbamate groups. The MoDTC compound of the compositions according to the invention may comprise from 1% to 40%, preferably from 2% to 30%, more preferably from 3% to 28%, even more preferably from 4% to 15% by mass of molybdenum, relative to the total mass of the MoDTC compound.

The MoDTC compound used according to the invention can be chosen from compounds whose core comprises two molybdenum atoms (dimeric MoDTC) and compounds whose core comprises three molybdenum atoms (trimeric MoDTC).

Trimeric MoDTC compounds generally have the formula Mo ₃ S _k L _n in which:

• k represents an integer at least equal to 4, preferably ranging from 4 to 10, advantageously from 4 to 7;
• n represents an integer ranging from 1 to 4 and
• L represents an alkyl dithiocarbamate group comprising from 1 to 100 carbon atoms, preferably from 1 to 40 carbon atoms, advantageously from 3 to 20 carbon atoms.

As examples of trimeric MoDTC compounds, mention may be made of the compounds and their methods of preparation described in patent application WO-98-26030.

Preferably, the MoDTC compound used in the lubricating composition according to the invention is a dimeric MoDTC compound. As examples of dimeric MoDTC compounds, mention may be made of the compounds and their methods of preparation described in patent application EP-0757093.

Dimeric MoDTC compounds are generally of formula (A):

(AT)

in which :

• R ¹ , R ² , R ³ and R ⁴ , which are identical or different, independently represent a hydrocarbon group chosen from alkyl, alkenyl, aryl, cycloalkyl and cycloalkenyl groups;
• X ¹ , X ² , X ³ and X ⁴ , which are identical or different, independently represent an oxygen atom or a sulfur atom.

Advantageously, R ¹ , R ² , R ³ and R ⁴ , which are identical or different, independently represent an alkyl group comprising from 4 to 18 carbon atoms or an alkenyl group comprising from 2 to 24 carbon atoms.

Also advantageously, X ¹ , X ² , X ³ and X ⁴ can be identical and represent a sulfur atom or else be identical and represent an oxygen atom. Also advantageously, X ¹ and X ² can represent a sulfur atom and X ³ and X ⁴ can represent an oxygen atom. Also advantageously, X ¹ and X ² can represent an oxygen atom and X ³ and X ⁴ can represent a sulfur atom.

The MoDTC compound of formula (A) can also be chosen from at least one symmetrical MoDTC compound, at least one asymmetrical MoDTC compound and combinations thereof. By symmetrical MoDTC compound is meant a MoDTC compound of formula (A) in which the R ¹ , R ² , R ³ and R ⁴ groups are identical. By asymmetric MoDTC compound is meant a MoDTC compound of formula (A) in which the R ¹ and R ² groups are identical, the R ³ and R ⁴ groups are identical and the R ¹ and R ² groups are different from the R ³ groups. and R ⁴ .

Advantageously, the lubricating composition according to the invention may comprise a mixture of at least one symmetrical MoDTC compound and at least one asymmetric MoDTC compound. More advantageously, R ¹ and R ² , which are identical, then represent an alkyl group comprising from 5 to 15 carbon atoms and R ³ and R ⁴ , which are identical to and different from R ¹ and R ² , represent an alkyl group comprising from 5 to 15 carbon atoms. Preferably, R ¹ and R ² , which are identical, represent an alkyl group comprising from 6 to 10 carbon atoms and R ³ and R ⁴ represent an alkyl group comprising from 10 to 15 carbon atoms.

Similarly, R ¹ and R ² , which are identical, can represent an alkyl group comprising from 10 to 15 carbon atoms and R ³ and R ⁴ can represent an alkyl group comprising from 6 to 10 carbon atoms.

Also, R ¹ and R ² , R ³ and R ⁴ , which are identical, can represent an alkyl group comprising from 5 to 15 carbon atoms, preferably from 8 to 13 carbon atoms.

Advantageously, the MoDTC compound is chosen from the compounds of formula (A) in which:

• X ¹ and X ² represent an oxygen atom,
• X ³ and X ⁴ represent a sulfur atom,
• R ¹ represents an alkyl group comprising 8 carbon atoms or an alkyl group comprising 13 carbon atoms,
• R ² represents an alkyl group comprising 8 carbon atoms or an alkyl group comprising 13 carbon atoms,
• R ³ represents an alkyl group comprising 8 carbon atoms or an alkyl group comprising 13 carbon atoms,
• R ⁴ represents an alkyl group comprising 8 carbon atoms or an alkyl group comprising 13 carbon atoms.

Thus, advantageously, the MoDTC compound can be chosen from the compounds of formula (A1)

(A1)

in which R ¹ , R ² , R ³ and R ⁴ are as defined for formula (A).

Advantageously, the MoDTC compound is a mixture:

• a MoDTC compound of formula (A1) in which R ¹ , R ² , R ³ and R ⁴ represent an alkyl group comprising 8 carbon atoms,
• of a MoDTC compound of formula (A1) in which R ¹ , R ² , R ³ and R ⁴ represent an alkyl group comprising 13 carbon atoms, and
• of a MoDTC compound of formula (A1) in which R ¹ and R ² represent an alkyl group comprising 13 carbon atoms and R ³ and R ⁴ represent an alkyl group comprising 8 carbon atoms, and/or
• of a MoDTC compound of formula (A1) in which R ¹ and R ² represent an alkyl group comprising 8 carbon atoms and R ³ and R ⁴ represent an alkyl group comprising 13 carbon atoms.

The ratio (S/O) of the number of sulfur atoms to the number of oxygen atoms of the MoDTC compound can generally vary from (1/3) to (3/1).

As specific examples of MoDTC compounds, mention may be made of the Molyvan L®, Molyvan 807® or Molyvan 822® products marketed by R.T Vanderbilt Company or the Sakuralube 200®, Sakuralube 165®, Sakuralube 525® or Sakuralube 600® products marketed by Adeka company.

The lubricating composition used according to the invention can also be implemented with an organomolybdenum compound chosen from the MoDTC compounds described in patent application WO-2012-141855.

Similarly, it can be implemented with a complex organomolybdenum compound or a MoDTP compound chosen from the compounds described in patent applications WO-2014-076240 and FR-3014898.

Advantageously, the MoDTP compound is chosen from the compounds of formula (B)

(B)

in which R ⁵ , R ⁶ , R ⁷ and R ⁸ , which are identical or different, independently represent a hydrocarbon group chosen from alkyl, alkenyl, aryl, cycloalkyl or cycloalkenyl groups.

As examples of MoDTP compounds, mention may be made of the Molyvan L® product marketed by the company R.T Vanderbilt Company or the Sakura-lube 300® or Sakura-lube 310G® products marketed by the company Adeka.

The invention can also be implemented with a complex organomolybdenum compound free of sulfur and phosphorus. This organomolybdenum complex free of sulfur and phosphorus can be prepared using amide-type ligands, mainly prepared by reacting a source of molybdenum, for example molybdenum trioxide, and an amine derivative and acids fat comprising for example from 4 to 28 carbon atoms, preferably from 8 to 18 carbon atoms. Examples of fatty acids are derived from vegetable or animal oils. This organomolybdenum complex can be prepared according to the methods described in patents US-4889647, EP-0546357, US-5412130, EP-1770153. A preferred organomolybdenum complex is obtained by reaction:

(i) a fatty acid or a fatty substance of the mono-, di- or tri-glyceride type,

(ii) of an amine source of formula (C):

(VS)

in which R ⁹ and R ¹⁰ , identical or different, independently represent an OH or NH ₂ group,

(iii) a source of molybdenum chosen from molybdenum trioxide or molybdates, preferably ammonium molybdate, in an amount sufficient to provide from 0.1 to 30%, preferably from 2 to 8.5%, in mass of molybdenum relative to the mass of complex.

Preferably, the organomolybdenum complex comprises at least one compound of formula (D) or of formula (E) or their mixture:

in which :

• L ¹ and L ² , identical or different, independently represent O or NH,
• Q ¹ and Q ² , which are identical or different, independently represent a linear or branched, saturated or unsaturated alkyl group, comprising from 3 to 30 carbon atoms, preferentially from 3 to 20 carbon atoms, advantageously from 7 to 17 carbon atoms.

This organomolybdenum complex can be prepared by reaction:

(i) a fatty acid or a fatty substance of the mono-, di- or tri-glyceride type,

(ii) diethanolamine or 2-(2-aminoethyl) aminoethanol,

(iii) a source of molybdenum chosen from molybdenum trioxide or molybdates, preferably ammonium molybdate, in an amount sufficient to provide 0.1 to 20% by mass of molybdenum relative to the mass of complex.

More preferably, the organomolybdenum complex comprises at least one compound of formula (D1) or of formula (D2) or their mixture:

in which Q ¹ independently represents a linear or branched, saturated or unsaturated alkyl group, comprising from 3 to 30 carbon atoms, preferentially from 3 to 20 carbon atoms, advantageously from 7 to 17 carbon atoms.

Borated dispersant(s)

The lubricating composition according to the invention further comprises one or more boron dispersant(s), such that the amount of boron element in the lubricating composition ranges from 10 to 300 ppm by weight, preferably from 20 to 300 ppm by weight, relative to the total weight of the lubricating composition.

The amount of boron element in the lubricating composition according to the invention can be measured according to standard ASTM D 5185.

According to one embodiment, the lubricating composition comprises from 0.01% to 10% by weight, preferably from 0.01% to 5% by weight, of borated dispersan(s), relative to the total weight of the lubricating composition.

Preferably, the borated dispersant(s) are chosen from borated succinimides, typically from borated polyisobutene succinimides.

Base oil(s)

The lubricating composition according to the invention comprises one or more base oils. This base oil can be chosen from many oils. The base oil of the lubricating composition according to the invention may in particular be chosen from oils of mineral or synthetic origin 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 mixtures thereof.

Saturates content Sulfur content Viscosity index (VI) Group I
Mineral oils < 90% > 0.03% 80 ≤ IV < 120 Group II
Hydrocracked oils ≥ 90% ≤0.03% 80 ≤ IV < 120 Group III
Hydrocracked or hydro-isomerized oils ≥ 90% ≤0.03% ≥ 120 Group IV polyalphaolefins (PAO) Group V esters and other bases not included in groups I to IV

The mineral base oils useful 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, desalphatation, solvent dewaxing, hydrotreating, hydrocracking, hydroisomerization and hydrofinishing. Blends of synthetic and mineral oils can also be used.

There is generally no limitation as to the use of different lubricating bases to produce the lubricating compositions according to the invention, except that they must have properties, in particular of viscosity, viscosity index, sulfur content , resistance to oxidation, suitable for use in engines.

The base oils of the lubricating compositions used according to the invention can also be chosen from synthetic oils, such as certain esters of carboxylic acids and alcohols, polyalkylene glycols (PAG), as well as from polyalphaolefins.

In one embodiment of the invention, the lubricating composition according to the invention comprises at least one Group II oil and/or at least one Group III oil.

Typically, the base oil or oils represent at least 50% by weight, preferably at least 60% by weight, more preferably at least 70% by weight, even more preferably at least 75% by weight, of the total weight of the lubricating composition.

Thus, according to one embodiment, the lubricating composition comprises from 50% to 99.89% by weight, preferably from 70% to 99.5% by weight, more preferably from 80% to 99% by weight of oil basestock(s), preferably including at least one Group II oil and/or at least one Group III oil and/or at least one Group IV oil and/or at least one Group V oil.

Other additive(s)

According to a particular embodiment, the lubricating composition also comprises one or more other additives.

The other preferred additives for the lubricating composition according to the invention are chosen from detergent additives, anti-wear additives, friction modifier additives with the exception of molybdenum-based friction modifiers, extreme pressure additives, dispersants other than the boron dispersants defined above, pour point improvers, viscosity index improvers, anti-foaming agents, thickeners and mixtures thereof.

Preferably, when they are present, the additives chosen from detergent additives, anti-wear additives, friction modifier additives with the exception of molybdenum-based friction modifiers, extreme pressure additives, dispersants other than boron dispersants defined above, pour point improvers, viscosity index improvers, anti-foaming agents, thickeners and mixtures thereof, constitute up to 20% by weight, preferably from 0, 1% to 15% by weight, more preferably 1% to 10% by weight, of the total weight of the lubricating composition.

According to one embodiment, the lubricating composition further comprises at least one detergent. Detergent additives generally reduce the formation of deposits on the surface of metal parts by dissolving secondary products of oxidation and combustion. The detergent additives which can be used in the lubricating composition according to the invention are generally known to those skilled in the art. Detergent additives can be anionic compounds comprising a long lipophilic hydrocarbon chain and a hydrophilic head. The associated cation can be a metal cation of an alkali or alkaline earth metal. The detergent additives are preferably chosen from alkali metal or alkaline-earth metal salts of carboxylic acids, sulfonates, salicylates, naphthenates, as well as phenate salts. The alkali and alkaline-earth metals are preferably calcium, magnesium, sodium or barium. These metallic salts generally comprise the metal in a stoichiometric quantity or else in excess, therefore in a quantity greater than the stoichiometric quantity. These are then overbased detergent additives ; the excess metal providing 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, preferentially a carbonate .

According to a particular embodiment, the lubricating composition comprising at least one detergent chosen from detergents based on calcium, detergents based on magnesium, and their mixture. According to a particular embodiment, the lubricating composition according to the invention comprises at least one calcium-based detergent and at least one magnesium-based detergent.

Advantageously, the lubricating composition according to the invention may comprise from 2 to 4% by weight of detergent additive(s) relative to the total mass of the lubricating composition.

Advantageously, the lubricating composition according to the invention may also additionally comprise at least one non-boronated dispersing agent. The non-boronated dispersing agent can be chosen from Mannich bases, succinimides and their derivatives. According to one embodiment, the non-boronated dispersant(s) can be chosen from non-boronated polyisobutene succinimide, and mixtures thereof.

Also advantageously, the lubricating composition according to the invention may comprise from 0.2% to 10% by mass of non-boronated dispersing agent, relative to the total mass of the lubricating composition.

The lubricating composition used according to the invention may comprise at least one pour point-improving additive or PPD agent ( for pour point depressant or pour point reduction agent). By slowing down the formation of paraffin crystals, the pour point reducing agents generally improve the cold behavior of the lubricating composition used according to the invention. As examples of pour point reducing agents, mention may be made of polyalkyl methacrylates (different from the copolymer of the invention), polyacrylates (different from the copolymer of the invention), polyarylamides, polyalkylphenols, polyalkylnaphthalenes, alkylated polystyrenes.

The lubricating composition according to the invention may also comprise at least one anti-wear additive, at least one extreme pressure additive or mixtures thereof. Preferably, the lubricating composition used according to the invention comprises at least one anti-wear additive.

Anti-wear additives and extreme pressure additives protect friction surfaces by forming a protective film adsorbed on these surfaces. There are a wide variety of anti-wear additives. Preferably, for the lubricating composition used according to the invention, the anti-wear additives are chosen from phospho-sulphur additives such as metal alkylthiophosphates, in particular zinc alkylthiophosphates, and more specifically zinc dialkyldithiophosphates or ZnDTP. The preferred compounds are of formula Zn((SP(S)(OR ^a )(OR ^b )) ₂ , in which R ^a and R ^b , which are identical or different, independently represent an alkyl group, preferably an alkyl group comprising from 1 to 18 carbon atoms.Amine phosphates are also anti-wear additives which can be used in the lubricating composition used 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 generate ash These effects can be minimized by partially replacing the amine phosphates with additives that do not provide phosphorus, such as, for example, polysulphides, in particular sulphur-containing olefins.

Advantageously, the lubricating composition according to the invention may comprise from 0.01 to 6% by mass, preferentially from 0.05 to 4% by mass, more preferentially from 0.1 to 2% by mass relative to the mass total of lubricating composition, anti-wear additives and extreme pressure additives.

Advantageously, the lubricating composition according to the invention may comprise at least one friction modifier additive different from the molybdenum friction modifier defined in the present invention. The friction modifier additive can be selected from a compound providing metallic elements and an ash-free compound. Among the compounds providing metallic elements, mention may be made of complexes of transition metals such as Sb, Sn, Fe, Cu, Zn, the ligands of which may be hydrocarbon compounds comprising oxygen, nitrogen, sulfur or of phosphorus. Ash-free friction modifier additives are generally of organic origin and can be selected from fatty acid and polyol monoesters, 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.

Advantageously, the lubricating composition according to the invention may comprise from 0.01% to 2% by mass or from 0.01% to 5% by mass, preferably from 0.1% to 1.5% by mass or from 0.1% to 2% by mass relative to the total mass of the lubricating composition, of friction modifier additive.

Advantageously, the lubricating composition according to the invention may comprise at least one antioxidant additive. The antioxidant additive generally makes it possible to delay the degradation of the lubricating composition in service. This degradation can in particular result in the formation of deposits, in the presence of sludge or in an increase in the viscosity of the lubricating composition. Antioxidant additives act in particular as free radical inhibitors or hydroperoxide destroyers. Among the antioxidant additives commonly employed, mention may be made of antioxidant additives of the phenolic type, antioxidant additives of the amine type, phosphosulfur antioxidant additives. Some of these antioxidant additives, for example phosphosulfur antioxidant additives, can be ash generators. The phenolic antioxidant additives may be ash-free or may be in the form of neutral or basic metal salts. The antioxidant additives may in particular be chosen from sterically hindered phenols, sterically hindered phenol esters and sterically hindered phenols comprising a thioether bridge, diphenylamines, diphenylamines substituted with at least one C ₁ -C ₁₂ alkyl group, 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 of which at least one carbon vicinal to the carbon carrying the alcohol function is substituted by at least one C ₁ -C ₁₀ alkyl group, preferably a C ₁ -C ₆ alkyl group, preferably a C ₄ alkyl group, preferably by the ter-butyl group. Amino compounds are another class of antioxidant additives that can be used, possibly in combination with phenolic antioxidant additives. Examples of amino compounds are aromatic amines, for example aromatic amines of formula NR ^c R ^d R ^e in which R ^c represents an aliphatic group or an optionally substituted aromatic group, R ^d represents an optionally substituted aromatic group, R ^e represents a hydrogen atom, an alkyl group, an aryl group or a group of formula R ^f S(O) _z R ^g in which R ^f represents an alkylene group or an alkenylene group, R ^g represents an alkyl group, a alkenyl group or an aryl group and z represents 0, 1 or 2. Sulfurized alkyl phenols or their alkali metal and alkaline earth metal salts can also be used as antioxidant additives. Another class of antioxidant additives is that of copper compounds, for example copper thio- or dithio-phosphates, salts of copper and of carboxylic acids, dithiocarbamates, sulphonates, phenates, copper acetylacetonates. Copper I and II salts, succinic acid or anhydride salts can also be used. The lubricating composition used 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 used according to the invention comprises from 0.5 to 2% by weight relative to the total mass of the composition, of at least one antioxidant additive.

Advantageously, the lubricating composition can also comprise at least one polymer improving the viscosity index different from the copolymer defined in the present invention. Examples of polymers improving the viscosity index include polymer esters, homopolymers or copolymers, hydrogenated or non-hydrogenated, of styrene, butadiene and isoprene, polymethacrylates (PMA). Also advantageously, the lubricating composition according to the invention may comprise from 0.1 to 15% by mass relative to the total mass of the lubricating composition of a polymer improving the viscosity index different from the copolymer defined herein. invention.

Typically, the lubricating composition according to the invention has a kinematic viscosity at 100° C. ranging from 3.8 mm²/s to 21.9 mm²/s. Kinematic viscosity can be measured according to ASTM D445.

Apps

The invention also relates to the use, in a lubricating composition comprising a base oil, one or more molybdenum friction modifiers and one or more boron dispersants, of a copolymer as defined above for improving the cold stability of said lubricating composition.

In particular, the lubricating composition comprising the base oil, the molybdenum friction modifier(s), the boron dispersant(s) and the copolymer of the invention has improved cold stability compared to the composition free of the copolymer.

By "cold stability" is meant within the meaning of the invention the ability of a lubricating composition to retain its physical homogeneity during prolonged storage, in particular of several weeks, at a low temperature, in particular at a temperature of 0°C. In particular, a composition having good cold stability does not present problems of sedimentation or of formation of deposits during prolonged storage at low temperature.

The cold stability of a lubricating composition can typically be evaluated as follows:

50 mL of the lubricating composition to be tested are poured into a test tube before being placed in a refrigerated chamber.

The state of the composition is then visually assessed based on storage time.

The following quotation is used:

- OK: the status of the composition is unchanged. No trace of deposit is observed,

- TRACE: the presence of slight traces of deposit is observed,

- DEPOT: the formation of deposits is observed,

- CLOUDY: the lubricating composition is cloudy due to the formation of a large amount of deposits.

According to one embodiment, the copolymer is as defined previously in the context of the lubricating composition according to the invention.

According to one embodiment, the molybdenum friction modifier(s) are as defined above in the context of the lubricating composition according to the invention.

According to one embodiment, the boron dispersant(s) are as defined above in the context of the lubricating composition according to the invention.

According to one embodiment, the base oil or oils are as defined above.

According to one embodiment, the lubricating composition is as defined above, after addition of the copolymer.

According to one embodiment, the copolymer is used at a rate of 0.1 to 10% by weight of dry matter, preferably from 0.5 to 5% by weight of dry matter, more preferably from 0.8 to 3% by weight of dry matter, relative to the total weight of the lubricating composition (after addition of the copolymer).

The invention also relates to the use of the lubricating composition according to the invention for lubricating the parts of an engine such as a motor vehicle engine.

The invention also relates to a method for lubricating at least one part of an engine, preferably of a vehicle engine, comprising bringing at least one part of the engine into contact with the lubricating composition according to the invention. .

The invention also relates to a method for reducing the friction occurring inside an engine, said method comprising the use of a combination of a copolymer as defined above, a friction modifier molybdenum and a boron dispersant in a lubricating composition comprising a base oil.

The invention also relates to a method making it possible to improve the fuel economy (FE or fuel eco ) properties of a lubricating composition, said method comprising the use of a combination of a copolymer as defined above, a molybdenum friction modifier and a boron dispersant in a lubricating composition comprising a base oil.

The invention also relates to a method making it possible to improve the cold stability properties (typically at 0° C.) of a lubricating composition, said method comprising the use of a combination of a copolymer as defined above , a molybdenum friction modifier and a boron dispersant in a lubricating composition comprising a base oil.

The molybdenum friction modifier, the boron dispersant and the copolymer are then provided separately or else in the form of a combination within the lubricating composition.

In the uses and methods of the invention, the copolymer, the molybdenum friction modifier, the boron dispersant and more generally the resulting lubricating composition may have one or more of the characteristics defined above in the context of the lubricating composition according to 'invention.

The particular, advantageous or preferred characteristics of the combined use according to the invention define particular, advantageous or preferred combinations which can be used according to the invention.

The different aspects of the invention can be illustrated by the examples which follow.

Example 1: preparation of lubricating compositions

The lubricating compositions are prepared by mixing the compounds described in Table 2, at a temperature of the order of 60°C. The percentages indicated correspond to percentages by mass relative to the total mass of the composition. Composition CL1 is a composition according to the invention and composition CC1 is a comparative composition outside the invention.

CL1 CC1 Base oils (% weight) 83.9 83.9 Copolymer 1 according to the invention (% dry weight) 5.0 - Copolymer 2 outside the invention (% dry weight) - 5.0 Additive package (%wt) 10.1 10.1 Additive to lower the pour point (%wt) 0.2 0.2 Of which
boron content (ppm by weight) 39 39 Friction modifiers: Mo-DTC (Sakuralube 525® from Adeka) (% weight) 0.8 0.8 Of which
molybdenum content (ppm by weight) 950 950

Copolymer 1 (according to the invention) is as defined in US 2017/0009177 A1.

Copolymer 2 (outside the invention) is as defined in WO 2012/081180 A1.

The additive package includes a calcium-based detergent, a magnesium-based detergent, and a boron succinimide dispersant.

Example 2: performance evaluation of friction

The ability of the lubricating compositions prepared above to reduce the friction occurring in an engine are evaluated as follows:

The test is carried out using a Nissan MR20DD engine, whose power is 108 kw at 5600 rpm, driven by an electric generator making it possible to impose a rotation speed of between 550 and 4400 rpm while that a torque sensor makes it possible to measure the frictional torque generated by the movement of parts in the engine. The friction torque induced by the lubricating composition to be tested is compared, for each engine speed and for each average torque at each temperature, with that induced by the reference lubricating composition (SAE 0W16) which was evaluated before and after the composition. lubricant to test.

The higher the value of the gain in friction, the more the lubricating composition makes it possible to reduce the friction occurring in the engine.

The conditions of this test are as follows.

The tests are carried out according to the following sequence:

- rinsing the engine with a detergent additive for lubricating oil comprising one rinse, followed by two rinses with a reference lubricant composition of grade 0W-12 comprising 81.7% by mass of base oil, 17.8% by mass of Common Additives (4.4% Viscosity Index Improver, 0.5% Oxidizer, 0.20% Pour Point Depressant and 12.7% Additive Pack) , and 0.05% by mass of molybdenum dithiocarbamate (MoDTC), relative to the total mass of the base oil;

- measurement of the friction torque at the two different temperatures indicated below on the engine using the reference lubricating composition;

- rinsing of the engine with a detergent additive for lubricating oil comprising a rinse, followed by two rinses with a lubricating composition to be evaluated;

- measurement of the friction torque at two different temperatures on the engine using the lubricating composition to be evaluated;

- rinsing of the engine with a detergent additive for lubricating oil comprising a rinse, followed by two rinses with the reference lubricating composition; And

- measurement of the friction torque at the two different temperatures indicated below on the engine using the reference lubricating composition.

The speed ranges, the speed variation and the temperature were chosen in agreement with Nissan, to be representative of the WLTC cycle.

The instructions implemented are:

- Water temperature at engine outlet: 50°C/80°C +/- 0.5°C

- Oil temperature ramp: 50°C/80°C +/- 0.5°C

The results obtained are shown in Table 3.

CL1 CC1 Gain in friction
T = 50°C 1.4% 1.2% Gain in friction
T= 8 0°C 1.8% 1.4%

The lubricating composition according to the invention CL1 has a gain in friction, measured at 50° C. and 80° C., greater than that of the comparative composition CC1 . The composition according to the invention CL1 therefore makes it possible to reduce more significantly the friction occurring in an engine, compared to the comparative composition CC1 . In particular, the copolymer of the invention makes it possible to reduce the friction occurring inside an engine.

It is known to those skilled in the art that the reduction in friction occurring in the engine has a direct impact on the fuel consumption of the engine: the less friction there is, the less fuel the engine consumes. Thus, the copolymer defined in the invention makes it possible to improve the FE properties of the lubricating composition.

Example 3: Evaluation of cold stability

The cold stability of the lubricating compositions prepared above is evaluated as follows:

50 mL of the lubricating composition to be tested are poured into a test tube before being placed in a refrigerated chamber.

The state of the composition is then visually assessed based on storage time.

The following quotation is used:

- OK: the status of the composition is unchanged. No trace of deposit is observed,

- TRACE: the presence of slight traces of deposit is observed,

- DEPOT: the formation of deposits is observed,

- CLOUDY: the lubricating composition is cloudy due to the formation of a large amount of deposits.

The results obtained are shown in Table 4.

CL1 CC1 9 days at 0°C OK Deposits 7 weeks at 0°C OK Deposits

The lubricating composition according to the invention CL1 has better cold stability than the comparative composition CC1 . In particular, the composition according to the invention is stable even after 7 weeks of storage at 0°C. The copolymer defined in the invention therefore makes it possible to improve the cold properties of the lubricating composition.

Claims (10)

Lubricant composition comprising:
- at least one base oil,
- at least one friction modifier comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 100 ppm to 1500 ppm by weight, relative to the total weight of the lubricating composition,
- at least one boron dispersant, such that the amount of boron element in the lubricating composition ranges from 10 ppm to 300 ppm, relative to the total weight of the lubricating composition,
- from 0.1% to 10% by weight of dry matter, relative to the total weight of the lubricating composition, of a polymer comprising repeating units capable of being obtained by polymerization of monomers (a) of formula (I) :
(I)
in which :

• R ¹ represents a hydrogen atom or a methyl group,
• X ¹ represents a group chosen from: -O-, -O(AO) _m , or -NH-, each group A independently representing a C2-C4 alkylene group and m an integer ranging from 0 to 10,
• R ² is a polybutylene group, and
• P is equal to 0 or 1.

A lubricating composition according to claim 1, comprising:
- at least 50% by weight, relative to the total weight of the lubricating composition, of one or more base oils,
- from 0.01% to 10% by weight, relative to the total weight of the lubricating composition, of one or more friction modifiers comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 300 ppm at 1000 ppm by weight, relative to the total weight of the lubricating composition,
- from 0.01% to 10% by weight, relative to the total weight of the lubricating composition, of one or more boron dispersants, such that the amount of boron element in the lubricating composition ranges from 10 ppm to 300 ppm in weight, relative to the total weight of the lubricating composition,
- from 0.5% to 5% by weight of dry matter, relative to the total weight of the lubricating composition, of a copolymer obtainable by copolymerization of monomers (a) of formula (I) and monomers ( b) of formula (II):
(II)
in which :

• R ³ represents a hydrogen atom or a methyl group,
• X ² represents an -O- or -NH- group,
• R groups⁴ independently represent a C2-C4 alkylene group,
• R ⁵ represents a C1-C8 alkyl group, and
• Q is an integer ranging from 1 to 20.

Lubricating composition according to any one of Claims 1 to 2, comprising:
- at least 70% by weight, relative to the total weight of the lubricating composition, of one or more base oils,
- from 0.01% to 5% by weight, relative to the total weight of the lubricating composition, of one or more friction modifiers comprising molybdenum, such that the amount of molybdenum element in the lubricating composition ranges from 500 ppm at 1000 ppm by weight, relative to the total weight of the lubricating composition,
- from 0.01% to 5% by weight, relative to the total weight of the lubricating composition, of one or more boron dispersants, such that the amount of boron element in the lubricating composition ranges from 20 ppm to 300 ppm in weight, relative to the total weight of the lubricating composition,
- from 0.8% to 3% by weight of dry matter, relative to the total weight of the lubricating composition, of a copolymer comprising, relative to the total weight of the copolymer:
- from 1% to 50% by weight of units derived from monomers (a), and
- from 1% to 80% by weight of units derived from monomers (b). Lubricating composition according to any one of Claims 1 to 3, having a kinematic viscosity at 100°C, measured according to the ASTM D445 standard, ranging from 3.8 mm²/s to 21.9 mm²/s. Lubricating composition according to any one of Claims 1 to 4, in which the friction modifier comprising molybdenum is an organomolybdenum compound, in particular a compound chosen from a molybdenum dithiocarbamate derivative (MoDTC), a molybdenum dithiophosphate derivative (MoDTP) or a sulfur-free molybdenum complex, preferably a molybdenum dithiocarbamate derivative (MoDTC). Lubricating composition according to any one of the preceding claims, in which the borated dispersant is chosen from borated succinimides, preferably from borated polyisobutene succinimides. Use, in a lubricating composition comprising a base oil, one or more molybdenum friction modifiers and one or more boron dispersants, of a copolymer comprising repeating units obtainable by polymerization of monomers (a) of formula ( I):
(I)
in which :

• R ¹ represents a hydrogen atom or a methyl group,
• X ¹ represents a group chosen from: -O-, -O(AO) _m , or –NH-, each group A independently representing a C2-C4 alkylene group and m an integer ranging from 0 to 10,
• R ² is a polybutylene group, and
• P is equal to 0 or 1,

to improve the cold stability of said lubricating composition. Use of a lubricating composition according to any one of Claims 1 to 6, for lubricating the parts of a motor vehicle engine. Use according to claim 8, for reducing friction between engine parts. Use according to one of Claim 8, for reducing the fuel consumption of the engine.