EP4413105A1 - Compose spiro comme additif detergent dans des lubrifiants destines a des systemes de motorisation - Google Patents
Compose spiro comme additif detergent dans des lubrifiants destines a des systemes de motorisationInfo
- Publication number
- EP4413105A1 EP4413105A1 EP22802028.5A EP22802028A EP4413105A1 EP 4413105 A1 EP4413105 A1 EP 4413105A1 EP 22802028 A EP22802028 A EP 22802028A EP 4413105 A1 EP4413105 A1 EP 4413105A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- mass
- additives
- lubricating composition
- spiro compound
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M139/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing atoms of elements not provided for in groups C10M127/00 - C10M137/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C65/00—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C65/01—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups
- C07C65/03—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups monocyclic and having all hydroxy or O-metal groups bound to the ring
- C07C65/05—Compounds having carboxyl groups bound to carbon atoms of six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups containing hydroxy or O-metal groups monocyclic and having all hydroxy or O-metal groups bound to the ring o-Hydroxy carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/04—Esters of boric acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
- C10M159/12—Reaction products
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/28—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
- C10M2227/062—Cyclic esters
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/04—Detergent property or dispersant property
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/40—Low content or no content compositions
- C10N2030/45—Ash-less or low ash content
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/76—Reduction of noise, shudder, or vibrations
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/25—Internal-combustion engines
Definitions
- the present invention relates to the field of lubricating compositions, in particular lubricating compositions for the lubrication of engine systems, mobile or stationary, in particular gasoline, diesel, gas (liquefied natural, compressed or hydrogen) or dual fuel engines, in particular light and heavy vehicles.
- the invention provides access to a lubricant having a reduced content of metallic detergents conventionally used in the field of lubricants and, consequently, having a reduced level of ash, in particular sulphated ash, while maintaining good detergency properties.
- Lubricating compositions also called “lubricants”, are commonly used in engines for the main purposes of reducing the frictional forces between the various moving metal parts in the engines. They are also effective in preventing premature wear or even damage to these parts, and in particular to their surface.
- a lubricating composition is conventionally composed of a base oil with which several additives are generally associated, such as for example friction modifier additives, dedicated to stimulating the lubricating performance of the base oil, but also to providing additional performance.
- the lubricants intended for the lubrication of engines must satisfy several requirements. They must therefore combine good anti-wear and anti-corrosion performance, as well as good detergency and dispersion properties to reduce the formation of deposits.
- the lubricants in particular for gasoline, diesel, gas (liquefied natural, compressed or hydrogen) or dual fuel engines, have good detergency properties.
- the incomplete combustion of the fuel produces soot which can lead to sludge deposits, as well as carbon and varnish deposits.
- residual sulfur in the fuel burns in the combustion chamber to produce sulfur-derived acids. These acids are responsible for corrosion and wear in the engine and accelerate the degradation of the oil.
- Detergent additives are thus added to base oils to prevent the formation of deposits on the surface of metal parts, which are harmful to the engine, by dissolving secondary products of oxidation and combustion, and thus increase the life of the engine.
- the detergent additives commonly used are metal salts, in particular sulfonates, phenates, salicylates of alkali metals, in particular of calcium or magnesium, overbased or not.
- Diesel particulate filters (LAP or DPF for "Diesel particulate filter” in Anglo-Saxon terminology), for example, which capture particles (PM for “Particle Matter” in Anglo-Saxon terminology) from the exhaust flow, allow reduce diesel vehicle exhaust particulate emissions with soot filtration efficiency greater than 95%.
- Application WO2006/022934 describes a lubricating composition comprising a lubricating oil and a detergent/antioxidant additive produced from the reaction between an acidic organic compound and a boron compound.
- the present invention aims to propose a means for improving the detergency properties of lubricants intended for mobile or stationary motorization systems, in particular in light and heavy vehicles, while reducing the ash content.
- the invention relates, according to a first of its aspects, to the use, as a detergent additive in a lubricating composition intended for an engine system, of at least one spiro compound of formula (I) below: [Chem 1] in which :
- M is an atom chosen from boron (B) and aluminum (Al), in particular is a boron atom; ni and n2 are, independently of each other, 0, 1 or 2; And
- R represent, independently of each other, a hydrocarbon group comprising from 1 to 50 carbon atoms, in particular from 5 to 20 and more particularly from 5 to 15 carbon atoms.
- the spiro compound used according to the invention is of formula (I) above, in which M is a boron atom.
- the spiro compound is a compound called a "spiroboronate compound", of formula (!') below: wherein n1, n2 and R are as previously defined.
- detergent additive within the meaning of the present invention, is meant a compound which, introduced into a lubricant, makes it possible to provide and/or increase its detergency capacities and therefore to reduce, prevent, or even remove deposits in the engine system.
- spiro compound according to the invention will more simply denote a spiro compound of formula (I) as defined above, in particular a spiroboronate compound of formula (!') as defined above.
- spiro compounds considered according to the invention are described more precisely in the following text.
- the invention also relates, according to another of its aspects, to a lubricating composition intended for the lubrication of a motorization system, in particular of a light or heavy-duty motor vehicle, comprising at least:
- a lubricating composition according to the invention comprises, in addition to the said spiro compound(s) according to the invention, one or more other detergent additives, in particular chosen from the metallic detergent additives conventionally used in the field of lubricants, in particular based on calcium or magnesium.
- the detergency properties of the lubricant can be assessed by evaluating the performance of the lubricant in terms of thermal stability by an "MCT” test (for "Micro Coking Test” in English terminology) according to the GFC Lu-27-T standard. -07, as described in the examples. This test reports on the tendency of the lubricant to form deposits/varnish under high temperature conditions similar to those encountered in the hottest parts of the engine (from 230°C to 280°C).
- the thermal stability of the detergent according to the MCT test, potentiated by the addition of the spiro compound according to the invention, remains high even in the event of prolonged exposure of the lubricant to high temperatures.
- a lubricating composition according to the invention retains good detergency capacities, even after prolonged use, in other words even when it is used.
- used within the meaning of the invention, is meant a lubricating composition implemented during at least one oil change interval, that is to say over a distance traveled by the vehicle of between 10,000 and 30,000 km, preferably between 15,000 and 30,000 km.
- said spiro compound or compounds, implemented as detergent additives according to the invention generate little ash compared to conventional metallic detergents.
- the implementation of one or more spiro compounds advantageously makes it possible to increase the detergency capacities of a lubricating composition, without negatively impacting the content of ash generated by the lubricant.
- the addition of one or more spiro compounds according to the invention makes it possible to reduce the content of metallic detergents conventionally used in lubricants, for example based calcium or magnesium, and undesirable given the ashes they generate, while maintaining, or even improving, the detergency capacity of the lubricant, compared to a lubricant free of spiro compound.
- a lubricating composition according to the invention thus makes it possible to combine excellent detergency properties and a low level of ash, in particular sulphated ash.
- a lubricating composition according to the invention advantageously has good properties in terms of reducing the fuel consumption of motor vehicles, also called “Fuel Eco” properties, and, in fact, contributes to the reduction of CO2 emissions.
- the implementation of a spiro compound according to the invention in particular of the spiroboronate type, also makes it possible to significantly increase the stability to oxidation of the composition lubricating.
- the implementation of a spiro compound according to the invention, in particular of a spiroboronate compound according to the invention makes it possible to access a lubricant having excellent detergency properties, a reduced ash content and excellent oxidation stability properties.
- the spiro compounds according to the invention due in particular to the tetra-covalent configuration of the boron or aluminum atom, are not hydrolysable.
- the spiro compounds according to the invention in particular the spiroboronate compounds according to the invention, exhibit excellent stability when they are brought into contact with water (which would for example result from the combustion of fuel or the condensation).
- water which would for example result from the combustion of fuel or the condensation.
- the absence of decomposition/degradation of the spiro compounds in the presence of water makes it possible in particular to prevent, during the implementation of the lubricating composition according to the invention, the formation of boric acid, a product classified as CMR (carcinogenic, mutagenic and repro toxic).
- the invention also relates to a process or a method for increasing the detergency capacity of a lubricating composition intended for a mobile or stationary engine system, in particular of a lubricating composition implementing a reduced content of metallic detergents, comprising the addition to said lubricating composition of at least one spiro compound according to the invention.
- the process or method according to the invention advantageously makes it possible to increase the detergency capacity of said composition, while maintaining a low ash content.
- the lubricant according to the invention makes it possible to reduce and/or prevent the phenomena of abnormal combustion of the fuel, in particular pre-ignition, by particular low-speed pre-ignition (known as “Low Speed PreIgnition” or “LSPI”) and/or knocking in an engine lubricated by a lubricant according to the invention (Kocsis et al, “The Impact of Lubricant Volatility, Viscosity and Detergent Chemistry on Low Speed Pre-Ignition Behavior", SAE Int. J.
- the spiro compound is advantageously implemented according to the invention as a detergent additive in a lubricating composition, to prevent and/or reduce abnormal fuel combustion, in particular pre-ignition, in particular LSPI, and/or or knock, in an engine lubricated with said lubricating composition.
- abnormal combustion is meant any phenomenon during which all or part of the fuel mixture is ignited in an uncontrolled manner within the combustion chamber of an engine, in particular of a vehicle engine, in particular of a vehicle automobile.
- Abnormal combustion according to the invention more particularly means pre-ignition phenomena, including low-speed pre-ignition (LSPI); and knocking, including super-knock or mega-knock that may follow a pre-ignition event.
- LSPI low-speed pre-ignition
- knocking including super-knock or mega-knock that may follow a pre-ignition event.
- pre-ignition is meant to include the phenomenon of low frequency vibration producing a sound effect of snoring (or “Rumble”). More particularly, “pre-ignition” is low-speed pre-ignition (LSPI).
- LSPI low-speed pre-ignition
- the lubricants considered according to the invention advantageously having excellent detergency properties, a reduced ash content, good "Euel Eco” properties and reduction/prevention of abnormal fuel combustion phenomena, in particular LSPI, can be implemented for various motorization systems, mobile or stationary, in particular for motorization systems comprising a diesel, gasoline, gas or dual-fuel, in particular diesel or gasoline engine.
- motorization system within the meaning of the present invention, is meant a system comprising all the mechanical parts necessary for the intended mobile or stationary application and including at least one engine, in particular an internal combustion engine. It may be a combustion, gas, in particular hydrogen, ammonia, electric or hybrid engine system, depending on the nature of the engine(s) included in the engine system: combustion engine, gas engine, in particular hydrogen, ammonia and/or electric.
- a “mobile” motorization system is more particularly a motorization system implemented in vehicles, including light vehicles, heavy goods vehicles, so-called “off-road” mobile machines, or else marine vehicles.
- a mobile motorization system thus corresponds more particularly to the propulsion system of a vehicle.
- propulsion system within the meaning of the present invention, is meant a system comprising the mechanical parts necessary for the propulsion of a vehicle.
- the propulsion system more particularly includes an engine, a transmission and optionally a battery.
- the battery is itself generally made up of a set of electric accumulators, called cells.
- a “stationary” motorization system within the meaning of the invention is a motorization system including a stationary motor.
- a stationary motor For example, it can find applications in devices for the production of electrical energy. It may in particular be a gas-operated drive system, in particular a stationary gas-operated engine.
- a "Diesel engine” within the meaning of the invention is a combustion engine whose fuel is diesel.
- a lubricating composition according to the invention is implemented in a propulsion system of a light motor vehicle or of a heavy goods vehicle, preferably for a gasoline or diesel engine.
- the lubricating compositions according to the invention are particularly suitable for gasoline and diesel engine systems, equipped with exhaust gas post-treatment systems, such as particulate filters (DPF).
- DPF particulate filters
- the invention also relates, according to another of its aspects, to a process or a method for lubricating a motorization system, mobile or stationary, in particular a diesel, gasoline, gas or dual-fuel engine, in particular in a light or heavy vehicle, comprising a step of bringing at least one mechanical part of said system into contact with a lubricating composition as defined above.
- a process or a method for lubricating a motorization system mobile or stationary, in particular a diesel, gasoline, gas or dual-fuel engine, in particular in a light or heavy vehicle, comprising a step of bringing at least one mechanical part of said system into contact with a lubricating composition as defined above.
- FIG. 1 presents a histogram of the rating results according to the MCT test for the reference lubricants 1 and 2 and for the lubricating compositions according to the invention II and 12 supplemented with a spiro compound according to the invention, as described in examples 1 and 2.
- Figure 2 shows the particle size distribution for the emulsion of spiroboronate in water obtained after paddle stirring ( Figure 2a) and after Ultra-Turrax® stirring ( Figure 2b), as described in Example 4.
- Figure 3 shows the NMR spectra of pure spiroboronate (Figure 3a) and of the residue ( Figure 3b) obtained as described in Example 4.
- the invention is based on the implementation, in a lubricant for an engine system, of one or more specific spiro compounds, as an additive to improve the detergency of the lubricant.
- the invention can implement a single spiro compound or a mixture of at least two distinct spiro compounds, in particular three or four distinct spiro compounds, in particular as defined below.
- M is an atom chosen from boron and aluminum, in particular is a boron atom; ni and n2 are, independently of each other, 0, 1 or 2; And
- R represent, independently of each other, a hydrocarbon group comprising from 1 to 50 carbon atoms, in particular from 5 to 20 and more particularly from 5 to 15 carbon atoms.
- the R groups are only composed of carbon and hydrogen atoms.
- the hydrocarbon groups can in particular be alkyl, alkenyl, aryl or aralkyl groups.
- the substituents R represent, independently of each other, a hydrocarbon group, preferably an aliphatic chain, linear or branched, comprising from 3 to 50 carbon atoms, in particular from 3 to 30 carbon atoms, in particular from 5 to 25 carbon atoms, in particular from 5 to 20 carbon atoms and more particularly from 8 to 15 carbon atoms.
- substituents R can represent, independently of one another, an aliphatic, linear or branched chain, in particular an alkyl chain, preferably linear, from C1 to C50; in particular C3 to C30, in particular C5 to C25, in particular C5 to C20 and more particularly Cs to C15, for example Cio.
- n1 and n2 are equal to 0.
- n1 and n2 are equal to 1 or 2.
- the R groups, carried by the same cycle, can be identical or different.
- the spiro compound may be of formula (I) above, in which n1 and n2 are 1; the substituents R possibly being identical or different, preferably identical.
- the spiro compound is of formula (I) above, in which: n1 and n2 are 1; and the groups R, which are identical, represent alkyl groups, preferably linear, C1 to C50, in particular C3 to C30, in particular C5 to C25, in particular C5 to C20 and more particularly Cs to C15, even more preferentially in Cio.
- the spiro compound is of formula (I) in which M is a boron atom.
- the spiro compound can be a so-called spiroboronate compound, of formula (T) below:
- the spiro compound is of formula (I) in which M is an aluminum atom.
- the spiro compound can be a so-called spiroaluminate compound, of formula (I”) following: [Chem 4]
- n1, n2 and R are as previously defined.
- the invention thus relates, according to another of its aspects, to a spiro compound of formula (I) mentioned above, in which:
- - ni and n2 are, independently of each other, 0, 1 or 2, at least one of ni and n2 being 1 or 2; preferably n1 and n2 are 1;
- the R groups represent, independently of each other, a linear or branched aliphatic chain, in particular an alkyl chain, preferably linear, comprising from 5 to 50 carbon atoms, in particular from 6 to 30 carbon, in particular from 8 to 25 carbon atoms and more particularly from 10 to 15 carbon atoms.
- the invention relates to a compound of the spiroaluminate type of formula (I”) above, in which:
- - ni and n2 are, independently of each other, 0, 1 or 2, at least one of ni and n2 being 1 or 2; preferably n1 and n2 are 1;
- the R groups represent, independently of each other, a linear or branched aliphatic chain, in particular an alkyl chain, preferably linear, comprising from 5 to 50 carbon atoms, in particular from 6 to 30 carbon, in particular from 8 to 25 carbon atoms and more particularly from 10 to 15 carbon atoms.
- the compound of spiroaluminate type according to the invention is of formula (I”) in which:
- the groups R which are identical or different, preferably identical, represent alkyl chains, preferably linear, comprising from 5 to 50 carbon atoms, in particular from 6 to 30 carbon atoms, in particular from 8 to 25 carbon atoms and more particularly from 10 to 15 carbon atoms.
- the spiro compound used according to the invention can be prepared from at least salicylic acid or a derivative of salicylic acid and a boron compound or an aluminum compound.
- boron or aluminum compound in particular boric acid or aluminum hydroxide.
- the preparation of the spiro compound used in the lubricating composition according to the invention does not involve any step, subsequent to the reaction of salicylic acid or one of its derivatives with said boron or aluminum compound, of reaction with an amine compound, as is the case for example in the context of the preparation of the compounds proposed in applications WO2018/220007 and WO2018/220009.
- Salicylic acid and its derivatives of formula (Ia) above can be synthesized according to synthetic methods known to those skilled in the art or can be commercially available.
- the boron compound (in other words, based on boron) can be chosen in particular from boric acid (B(OH)3), boronic acids, boric and boronic esters, boron oxide and acid complexes boric.
- the boron compound can be chosen from boric acid; boron oxide; boric acid complexes; trialkyl borates, in particular in which the alkyl groups comprise independently of each other from 1 to 4 carbon atoms; boronic acids having a C1-C12 alkyl group; boric acids substituted with two alkyl groups, in particular C1 to C12; boric acids substituted with two aryl groups, in particular C6 to C12; boric acids substituted by one or two aralkyl groups, in particular C7 to C12, and derivatives of these compounds obtained by substitution of at least one alkyl group by one or more alkoxy groups.
- Boric acid complexes are in particular complexes of boron with one or more molecules comprising one or more alcohol functions.
- the boron compound is boric acid.
- the aluminum compound in other words, based on aluminium
- reaction can be carried out in a solvent medium consisting of one or more apolar solvents and/or practical polar solvents.
- the solvent medium may consist of one or more solvents chosen from naphtha, practical polar solvents, such as water and alcohols, for example methanol, ethanol, propanol, butanol; and their mixtures.
- the reaction between salicylic acid or one of its derivatives of formula (la) above and the boron or aluminum compound to obtain the desired spiro compound in particular the reaction between salicylic acid or one of its derivatives of formula (Ia) and the boron compound to obtain the desired spiroboronate compound, can be carried out in an apolar aprotic solvent medium, in particular in toluene.
- hydrocarbon group a radical saturated or not, linear, branched or cyclic, aromatic or not, comprising carbon and hydrogen
- aliphatic chain a hydrocarbon group consisting exclusively of carbon and hydrogen atoms, linear or branched, saturated or unsaturated, non-aromatic.
- an aliphatic chain is an alkyl chain
- alkyl a saturated, linear or branched aliphatic group; for example, a C x to C z alkyl represents a saturated carbon chain of x to z carbon atoms, linear or branched;
- alkenyl a mono- or poly-unsaturated, linear or branched aliphatic group
- a cyclic alkyl group for example a C x to C z cycloalkyl represents a cyclic carbon group of x to z carbon atoms, for example a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl;
- aryl a mono- or polycyclic aromatic group, in particular comprising between 6 and 10 carbon atoms.
- aryl group mention may be made of phenyl or naphthyl groups;
- aralkyl an aryl group as defined above, substituted by at least one alkyl group as defined above.
- the said spiro compound or compounds are advantageously implemented in a sufficient content to achieve the required level of detergency capacity of the lubricant.
- a small amount of spiro compound(s) in particular less than 2% by mass, in particular less than or equal to 1% by mass, relative to the total mass of said lubricating composition, makes it possible to significantly increase the detergency capacity of the lubricant.
- spiro compound(s) can be adjusted according to the nature of the lubricant, and more particularly taking into account the presence or not and the quantity implemented of other additive(s).
- s) detergent(s), in particular metal(s), for example calcium-based, present in the lubricant can be adjusted according to the nature of the lubricant, and more particularly taking into account the presence or not and the quantity implemented of other additive(s).
- s) detergent(s), in particular metal(s), for example calcium-based present in the lubricant.
- the said spiro compound or compounds considered according to the invention in particular as defined previously, can be implemented at a rate of 0.1 to 20% by mass, in particular from 0.2 to 15% by mass , in particular from 0.5 to 10%, and more particularly from 0.5 to 5.0% by mass, relative to the total mass of said lubricating composition.
- a lubricating composition as considered according to the invention comprises more particularly one or more base oils and, optionally, other additives conventionally considered in lubricating compositions.
- a lubricating composition comprises one or more base oils.
- base oils can be chosen from the base oils conventionally used in the field of lubricating oils, such as mineral, synthetic or natural, animal or vegetable oils or mixtures thereof.
- It can be a mixture of several base oils, for example a mixture of two, three or four base oils.
- the base oils of the lubricating compositions considered according to the invention may in particular be 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) and presented in Table A below or mixtures thereof. [Table 1]
- Mineral base oils include all types of base oils obtained by atmospheric and vacuum distillation of crude oil followed by refining operations such as solvent extraction, de-alpha removal, solvent dewaxing, hydrotreating, hydrocracking, hydroisomerization and hydrofinishing .
- Synthetic base oils can be esters of carboxylic acids and alcohols, polyalphaolefins or polyalkylene glycol (PAG) obtained by polymerization or copolymerization of alkylene oxides comprising from 2 to 8 carbon atoms, in particular of 2 to 4 carbon atoms.
- the polyalphaolefins used as base oils are for example obtained from monomers comprising 4 to 32 carbon atoms, for example from decene, octene or dodecene, and whose viscosity at 100° C. is between 1, 5 and 15 mm 2 .s -1 according to the ASTM D445 standard. Their average molecular mass is generally between 250 and 3000 according to the ASTM D5296 standard.
- Blends of synthetic and mineral oils, which may be biosourced, can also be used.
- a lubricating composition under consideration according to the invention comprises at least one base oil chosen from group II, III and IV oils of the API classification, and mixtures thereof.
- such a lubricating composition can comprise at least one group III base oil, in particular a mixture of at least two group III base oils.
- the base oils suitable for the invention may have a kinematic viscosity measured at 40° C. according to the ASTM D445 (KV40) standard ranging from 10 to 100 mm 2 /s, in particular from 12 to 50 mm 2 /s, more particularly from 15 to 40 mm 2 /s.
- KV40 kinematic viscosity measured at 40° C. according to the ASTM D445 (KV40) standard ranging from 10 to 100 mm 2 /s, in particular from 12 to 50 mm 2 /s, more particularly from 15 to 40 mm 2 /s.
- the base oils suitable for the invention may have a kinematic viscosity measured at 100° C. according to the ASTM D445 standard (KV 100) ranging from 1 to 15 mm 2 /s, in particular from 2 to 10 mm 2 /s, more particularly from 4 to 8 mm 2 /s.
- the base oil or oils may be present in a lubricating composition according to the invention in a content of at least 50% by mass, relative to its total mass, in particular at least 60% by mass, more particularly ranging from 60 to 99% by mass and preferably from 70 to 90% by mass.
- the oil or oils of group III represent(s) at least 50% by mass, in particular at least 60% by mass, more particularly between 70 and 100% by mass, for example between 80 and 100% by mass, of the total mass of base oils in the composition.
- a lubricating composition according to the invention may comprise all types of additives suitable for the intended use for the lubricant, as detailed in the following text, for example for use in motorization systems for light vehicles or heavy goods vehicles. , especially diesel engines.
- the additives are chosen so as not to significantly impact the ash content of the lubricating composition.
- additives can be introduced individually and/or in the form of a mixture, or "package of additives", like those already available for sale for the formulations of commercial lubricants for vehicle engines, of level of performance as defined by ACEA (Association of European Automobile Manufacturers) and/or API (American Petroleum Institute), well known to those skilled in the art.
- ACEA Association of European Automobile Manufacturers
- API American Petroleum Institute
- additives distinct from said spiro compound(s) may be chosen in particular from other detergent additives, distinct from said spiro compound(s), in particular metallic detergent additives, friction modifiers, anti-wear additives, extreme pressure additives , antioxidants, viscosity index (VI) improvers, pour point depressants (PPD), dispersants, antifoaming agents, thickeners, corrosion inhibitors, and mixtures thereof.
- a lubricating composition according to the invention comprises one or more additives chosen from other detergent additives, distinct from said spiro compound(s), in particular chosen from metallic detergent additives, viscosity index improvers, additives pour point, anti-wear additives, antioxidants and mixtures thereof.
- the lubricating composition under consideration according to the invention may comprise one or more other detergent additives, in particular one or more metallic detergent additives.
- metal detergents are known to those skilled in the art to provide high levels of detergency.
- these metal compounds have the disadvantage of generating sulphated ash.
- anionic compounds comprising a long lipophilic hydrocarbon chain and a hydrophilic head, the associated cation possibly being a metal cation of an alkali or alkaline earth metal.
- alkali metal or alkaline-earth metal salts of carboxylic acids are generally chosen from alkali metal or alkaline-earth metal salts of carboxylic acids, in particular sulfonates, salicylates, naphthenates, phenates, carboxylates and mixtures thereof.
- 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.
- overbased detergent additives the excess metal providing the overbased character to the additive detergent is then generally in the form of a metal salt insoluble in the base oil, for example a carbonate, a hydroxide, an oxalate, an acetate, a glutamate, preferentially a carbonate.
- a lubricating composition according to the invention comprises at least one metallic detergent additive, distinct from the spiro compounds according to the invention, in particular chosen from salts of alkali metals or alkaline-earth metals, overbased or not. , in particular among calcium salts, magnesium salts and mixtures thereof.
- a lubricating composition according to the invention intended for a motorization system, in particular for a light or heavy motor vehicle, comprises at least:
- At least one metallic detergent additive distinct from said spiro compound in particular as defined above, in particular chosen from calcium and magnesium salts and mixtures thereof.
- a lubricating composition according to the invention may comprise at least one calcium-based detergent additive, such as a sulphonate, a salicylate, a naphthenate, a phenate, a calcium carboxylate or a mixture thereof, in particular an overbased calcium-based detergent additive, for example with calcium carbonate.
- a calcium-based detergent additive such as a sulphonate, a salicylate, a naphthenate, a phenate, a calcium carboxylate or a mixture thereof, in particular an overbased calcium-based detergent additive, for example with calcium carbonate.
- the content of metallic detergent additives as defined above, undesirable with regard to the ash they generate, can be reduced, while retaining good detergency properties.
- the lubricating composition according to the invention may comprise less than 15% by mass, in particular less than 10% by mass and more particularly from 0.1 to 10% by mass, in particular from 0.5% to 5 0.0% by mass, of metal detergent additive(s) distinct from the spiro compounds according to the invention, relative to the total mass of said composition.
- the said metallic detergent additive(s) may be present in the lubricating composition so as to provide a content of metallic element(s), in particular calcium, of less than or equal to 6000 ppm, in particular ranging from 100 ppm to 4000 ppm, preferably from 250 ppm to 3000 ppm.
- a lubricating composition according to the invention thus has a sulphated ash content, determined according to the ASTM D-874 standard, of less than or equal to 2% by mass, in particular less than or equal to 1.5% by mass, and more particularly less than or equal to 1% by mass, relative to the total mass of said lubricating composition.
- a lubricating composition according to the invention may comprise:
- a lubricating composition under consideration according to the invention may also comprise one or more other additives, distinct from the said spiro compound(s), chosen from friction modifier additives, anti-wear additives, extreme pressure additives, antioxidants, viscosity index improvers, point depressant additives flow agents, dispersants, antifoaming agents, thickeners, corrosion inhibitors, and mixtures thereof.
- additives distinct from the said spiro compound(s), chosen from friction modifier additives, anti-wear additives, extreme pressure additives, antioxidants, viscosity index improvers, point depressant additives flow agents, dispersants, antifoaming agents, thickeners, corrosion inhibitors, and mixtures thereof.
- a lubricating composition considered according to the invention can also comprise at least one viscosity index (VI) improver.
- Viscosity index (VI) improvers in particular viscosity index improver polymers, help ensure good cold behavior and minimum viscosity at high temperatures.
- polymers improving the viscosity index mention may be made of polymeric esters, homopolymers or copolymers, hydrogenated or non-hydrogenated, of styrene, butadiene and isoprene, homopolymers or copolymers of olefins, such as such as ethylene or propylene, polyacrylates and polymethacrylates (PMA).
- a lubricating composition according to the invention comprises at least one viscosity index improver chosen from polymethacrylates (PMA) and hydrogenated polyisoprene-styrene (PISH), linear, grafted, comb-shaped or star-shaped, preferably in star.
- PMA polymethacrylates
- PISH hydrogenated polyisoprene-styrene
- the additive(s) improving the viscosity index may be present in a lubricating composition according to the invention in a content ranging from 1 to 15% by mass, in particular from 2 to 10% by mass, relative to the total mass. of the lubricating composition.
- a lubricating composition according to the invention is free of additive improving the viscosity index.
- a lubricating composition under consideration according to the invention may comprise at least one friction modifier additive.
- the friction modifier additives can be chosen from compounds providing metallic elements and compounds free of ash, preferably from compounds free of ash.
- transition metals such as Mo, Sb, Sn, Fe, Cu, Zn
- the ligands of which may be hydrocarbon compounds comprising oxygen, nitrogen, sulfur or phosphorus.
- the friction modifier additives are chosen from ash-free compounds, generally of organic origin and which can be more particularly chosen from monoesters of fatty acids and polyols, alkoxylated amines, alkoxylated fatty amines, fatty epoxides, borate fatty epoxides, fatty amines or fatty acid glycerol esters.
- the fatty compounds comprise at least one hydrocarbon group comprising from 10 to 24 carbon atoms.
- a lubricating composition comprises at least one friction modifier additive, in particular based on molybdenum.
- the molybdenum-based compounds can be chosen from molybdenum dithiocarbamates (Mo-DTC), molybdenum dithiophosphates (Mo-DTP), and mixtures thereof.
- a lubricating composition considered according to the invention may comprise from 0.01 to 5% by mass, preferably from 0.01 to 5% by mass, more particularly from 0.1 to 2% by mass or even more particularly from 0 1 to 1.5% by mass, relative to the total mass of the lubricating composition, of friction modifier additives.
- a lubricating composition according to the invention may comprise at least one antiwear and/or extreme pressure additive.
- Anti-wear additives and extreme pressure additives protect friction surfaces by forming a protective film adsorbed on these surfaces.
- the anti-wear additives are chosen from phosphosulfur additives such as metal alkylthiophosphates, in particular zinc alkylthiophosphates, and more specifically zinc dialkyldithiophosphates or ZnDTP.
- phosphosulfur 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 3 )(OR 4 ))2, in which R 3 and R 4 , 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 according to the invention.
- the phosphorus provided by these additives can act as a poison for the catalytic systems of automobiles because these additives generate ash.
- the extreme pressure and/or anti-wear additive(s) may be present in a lubricating composition according to the invention in a content ranging from 0.01 to 6% by mass, preferably from 0.05 to 4% by mass. , more preferably from 0.1 to 2% by mass relative to the total mass of lubricating composition.
- a lubricating composition considered according to the invention may comprise at least one antioxidant additive.
- Antioxidant additives are essentially dedicated to delaying 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. They act in particular as free radical inhibitors or destroyers of hydroperoxides.
- 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 can be ash-free or 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 C1-C12 alkyl group, N,N '-dialkyl-aryl-diamines and mixtures thereof.
- 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 C1-C10 alkyl group, preferably a C1-C6 alkyl group. , preferably a C4 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 5 R 6 R 7 in which R 5 represents an aliphatic group or an optionally substituted aromatic group, R 6 represents an aromatic group, optionally substituted, R 7 represents a hydrogen atom, an alkyl group, an aryl group or a group of formula R 8 S(O) Z R 9 in which R 8 represents an alkylene group or an alkenylene group, R 9 represents a 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.
- a lubricating composition considered according to the invention may contain all types of antioxidant additives known to those skilled in the art.
- the lubricating composition comprises at least one ash-free antioxidant additive.
- a lubricating composition considered according to the invention may comprise from 0.1 to 2% by mass, relative to the total mass of the composition, of at least one antioxidant additive.
- a lubricating composition considered according to the invention may comprise at least one pour point depressant additive (also called “PPD” agents for “Pour Point Depressant” in English).
- pour point depressants By slowing down the formation of paraffin crystals, pour point depressants generally improve the cold behavior of the lubricating composition.
- pour point reducing agents examples include polyalkyl methacrylates, poly acrylates, polyarylamides, polyalkylphenols, polyalkylnaphthalenes and alkylated polystyrenes.
- a lubricating composition considered according to the invention can also comprise at least one dispersing agent.
- the dispersing agents ensure the maintenance in suspension and the evacuation of the insoluble solid contaminants constituted by the secondary products of oxidation which are formed when the lubricating composition is in service. They can be chosen from Mannich bases, succinimides and their derivatives.
- a lubricating composition under consideration according to the invention may comprise from 0.2 to 10% by mass of dispersing agent(s), relative to the total mass of the composition.
- a lubricating composition under consideration according to the invention may also comprise at least one antifoam additive.
- the antifoam additives can be chosen from polar polymers such as polymethylsiloxanes or polyacrylates.
- a lubricating composition considered according to the invention may comprise from 0.01 to 3% by weight of antifoam additive(s), relative to the total weight of the lubricating composition.
- the package of additives can represent from 1% to 30% by mass relative to the total mass of the composition, in particular from 1 to 20% by mass, in particular from 3% to 15% by mass and more particularly from 5 to 15% by weight.
- a lubricating composition according to the invention may comprise, or even consist of:
- additives distinct from said spiro compound(s), chosen from other detergent additives, in particular metallic detergent additives, friction modifiers, anti-wear additives, extreme pressure additives, antioxidants, viscosity index (VI), pour point depressants (PPD), dispersants, antifoaming agents, thickeners, corrosion inhibitors, and mixtures thereof.
- a lubricating composition formulated according to the invention comprises, or even consists of:
- additive(s) chosen from among the other detergent additives, distinct from the said spiro compound(s), in particular chosen from metallic detergent additives; anti-wear agents; antioxidants; dispersants; viscosity index improvers and mixtures thereof; the contents being expressed relative to the total mass of said lubricating composition.
- a lubricating composition formulated according to the invention may comprise, or even consist of:
- lubricating composition optionally from 1% to 30% by weight, preferably from 3% to 20% by weight, of one or more other additives chosen from anti-wear agents, antioxidants, viscosity index improvers and mixtures thereof, contents being expressed relative to the total mass of said lubricating composition.
- a lubricating composition according to the invention may have a kinematic viscosity, measured at 40° C. according to the ASTM D445 standard, of between 20 mm 2 /s and 50 mm 2 /s, preferably between 25 mm 2 /s and 40 mm 2 /s.
- a lubricating composition according to the invention has a kinematic viscosity, measured at 100° C. according to the ASTM D445 standard, of between 2 mm 2 /s and 20 mm 2 /s, preferably between 4 mm 2 /s and 15 mm 2 /s.
- the lubricating compositions considered according to the invention can be intended for mobile or stationary motorization systems, in particular for petrol, diesel, gas or dual-fuel engines.
- the invention thus relates, according to another of its aspects, to the use of a composition as defined above, incorporating one or more spiro compounds as a detergent additive, to lubricate a mobile or stationary engine system.
- the lubricating compositions according to the invention may in particular be intended for engine systems including an internal combustion engine, and more particularly a diesel or gasoline fuel engine, preferably a diesel engine.
- they are implemented for the lubrication of a motorization system of a vehicle, more particularly of a light or heavy vehicle, for example trucks.
- DPF diesel particulate filters
- the MCT test evaluates the tendency of a composition to form deposits (or varnish) on a hot surface (coking). It takes into account the thermal stability of a composition in thin film, subjected to temperature conditions similar to those encountered in the hottest parts of the engine (230 to 280°C). These deposits and varnishes are measured by a video rater. The result is expressed in the form of a score out of 10, called merit, according to CEC M-02-A-78. The higher the MCT value, the better the thermal stability of the lubricating composition.
- test conditions are as follows:
- the temperature from which the deposition of varnish occurs is also determined. The higher this temperature, the better the thermal stability of the lubricating composition.
- Oxidation stability is evaluated by differential pressure scanning calorimetry, which determines the oxidation induction time, known as OIT (for "Oxidation Induction Time” in English terminology) for lubricating compositions. This is a standard procedure in the lubricating oil industry based on CEC L-85 T-99.
- the lubricating composition to be tested is heated to a high temperature (in the present case, isothermal at 50°C for 5 minutes, then increased to 210°C at a rate of 40°C/min, oxidation making at 210°C), and the time when the lubricant begins to break down is measured.
- a high temperature in the present case, isothermal at 50°C for 5 minutes, then increased to 210°C at a rate of 40°C/min, oxidation making at 210°C
- the effect of adding a spiroboronate compound was evaluated on two lubricants, denoted reference 1 and reference 2, intended for heavy goods vehicles, the composition of which is detailed in the following table.
- the lubricants are formulated by simply mixing the various components at 60°C.
- Additive package common in the field of lubricants and commercially available. It includes anti-wear agents of the type zinc dithiophosphate, detergents based on calcium and dispersants of the type PIBSI.
- Two lubricating compositions in accordance with the invention are prepared by supplementing reference lubricants 1 and 2 respectively with a spiroboronate compound in accordance with the invention (spiro compound of formula (I) in which M is an atom of boron, R each represent a decyl group and n1 and m are equal to 1), at a rate of 1% by weight relative to the reference lubricant.
- a spiroboronate compound in accordance with the invention spiro compound of formula (I) in which M is an atom of boron, R each represent a decyl group and n1 and m are equal to 1
- the rating results (MCT at 90 min) are collated in the following table and are presented in the histogram of Figure 1.
- the temperature values from which the formation of deposits (Toepôt) occurs are also collated in the table following.
- compositions according to the invention supplemented with a spiroboronate compound according to the invention, have an excellent rating, superior to those obtained with the reference lubricants, which testifies to a significantly increased thermal stability under high temperature conditions (from 230°C to 280°C).
- a spiroboronate compound according to the invention makes it possible to significantly increase the thermal stability of the lubricant.
- the lubricants will thus form less deposit/varnish under the conditions of implementation at the level of the motorization system of the vehicles, and thus have improved detergency properties.
- the reference lubricants and the lubricating compositions according to the invention, as prepared in example 1, are evaluated according to the MCT test modified to subject the layers of lubricant to high temperature (from 230 to 280° C.) for a duration three times longer. long (3 times 90 minutes). Such conditions make it possible to simulate aging of the lubricant.
- the rating results, under the different conditions of the MCT test, are collated in the following table, and are presented in the histogram of FIG. 1.
- the temperature values from which the formation of the deposits (Toepôt) occurs are also collected in the following table.
- the lubricants according to the invention retain excellent detergency properties even after repeated use of the lubricant.
- Two lubricating compositions in accordance with the invention are prepared on the basis of the comparative lubricants CC3 and CC4, in which 2% by mass of base oil are replaced by 2% by mass of spiroboronate compound according to the invention.
- the lubricants are formulated by simply mixing the various components at 60°C. [Table 5]
- Oxidation stability properties are evaluated according to the protocol based on the CEC L-85 T-99 standard, described above.
- OIT oxidation induction time
- the lubricating composition according to the invention also makes it possible to improve engine cleanliness.
- the spiroboronate compound tested is a spiro compound of formula (I) in which M is a boron atom, R each represent an octadecyl chain (C18) and n1 and n2 are equal to 1, in other words has the following formula:
- the compound spiroboronate was prepared from the previously synthesized salicylic acid derivative (2-hydroxy-5-octadecylbenzoic acid) and boric acid.
- Figure 2 shows the particle size distribution for the emulsion obtained after paddle stirring ( Figure 2a) and after Ultra-Turrax® stirring ( Figure 2b).
- the emulsion of spiroboronate in water was then passed to the rotary evaporator under vacuum, in order to evaporate the water.
- the residue after water evaporation was collected and analyzed by RMNIH.
- the NMR spectrum of the residue is compared to that of the pure spiroboronate compound.
- Figure 3 shows the NMR spectra of pure spiroboronate (Figure 3a) and of the residue obtained as previously described ( Figure 3b).
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Lubricants (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR2110620A FR3127953B1 (fr) | 2021-10-07 | 2021-10-07 | Composé spiro comme additif détergent dans des lubrifiants destinés à des systèmes de motorisation |
| PCT/EP2022/077850 WO2023057590A1 (fr) | 2021-10-07 | 2022-10-06 | Compose spiro comme additif detergent dans des lubrifiants destines a des systemes de motorisation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP4413105A1 true EP4413105A1 (fr) | 2024-08-14 |
Family
ID=79602210
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP22802028.5A Pending EP4413105A1 (fr) | 2021-10-07 | 2022-10-06 | Compose spiro comme additif detergent dans des lubrifiants destines a des systemes de motorisation |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US12460148B2 (fr) |
| EP (1) | EP4413105A1 (fr) |
| JP (1) | JP2024536411A (fr) |
| KR (1) | KR20240099252A (fr) |
| CN (1) | CN118339264A (fr) |
| FR (1) | FR3127953B1 (fr) |
| WO (1) | WO2023057590A1 (fr) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR3154120A1 (fr) | 2023-10-13 | 2025-04-18 | Totalenergies Onetech | Composition lubrifiante comportant une huile lubrifiante re-raffinée et un composé spiro |
| FR3158319A1 (fr) * | 2024-01-16 | 2025-07-18 | Totalenergies Onetech | Composition lubrifiante pour prévenir ou diminuer les frottements dans un système mécanique |
| FR3158318A1 (fr) * | 2024-01-16 | 2025-07-18 | Totalenergies Onetech | Composition lubrifiante pour prévenir ou diminuer les frottements dans un système mécanique |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2898359A (en) | 1953-01-09 | 1959-08-04 | Shell Dev | Iron carbonyl-cyclopentadiene complexes |
| US2763613A (en) | 1953-10-29 | 1956-09-18 | Shell Dev | Lubricating oil containing dicyclopentadienyl iron and an oil soluble organic divalent metal salt |
| DE1243811B (de) | 1964-06-16 | 1967-07-06 | Bayer Ag | Schmierstoffzusatzmittel |
| JPH07104608B2 (ja) * | 1987-07-03 | 1995-11-13 | キヤノン株式会社 | 静電荷像現像用トナ− |
| DE4435548A1 (de) | 1994-10-05 | 1996-04-11 | Rhein Chemie Rheinau Gmbh | Stabilisierte Schmierstoff-Grundsubstanz |
| US6143702A (en) | 1998-10-09 | 2000-11-07 | Exxon Research And Engineering Company | Lubricating oils of enhanced oxidation stability containing n-phenyl-naphthyl amines, or substituted derivatives of n-phenyl naphthyl amine and carbodiimide acid scavengers |
| US6235687B1 (en) | 1998-10-09 | 2001-05-22 | Exxon Research And Engineering Company | Method for producing lubrication oils possessing anti rust properties containing acidic anti rust additive and acid scavengers |
| GB2427410A (en) | 2003-05-12 | 2006-12-27 | Southwest Res Inst | High octane lubricants for knock mitigation in flame propagation engines |
| US7618467B2 (en) * | 2004-01-29 | 2009-11-17 | Chemtura Corporation | Detergent / anti-oxidant additives for fuels and lubricants |
| US7691793B2 (en) * | 2004-07-21 | 2010-04-06 | Chemtura Corporation | Lubricant additive containing alkyl hydroxy carboxylic acid boron esters |
| US7516173B2 (en) | 2004-08-04 | 2009-04-07 | Intel Corporation | Carry-skip adder having merged carry-skip cells with sum cells |
| US20060122077A1 (en) | 2004-12-03 | 2006-06-08 | Bruce Wilburn | Compositions comprising at least one carbodiimide |
| EP2290043B1 (fr) | 2009-08-24 | 2012-08-29 | Infineum International Limited | Composition d'huile de lubrification comprenant un métal dialkyldithiophosphate et un carbodiimide |
| SE535675C2 (sv) * | 2011-03-22 | 2012-11-06 | Högprestandasmörjmedel och tillsatser till smörjmedel för järnhaltiga och icke järnhaltiga material | |
| US8643528B1 (en) | 2012-08-02 | 2014-02-04 | Texas Instruments Incorporated | Analog-to-digital converter |
| US9752093B2 (en) | 2015-06-04 | 2017-09-05 | Chevron Oronite Company Llc | Borated polyol ester of hindered phenol antioxidant/friction modifier with enhanced performance |
| US20170015933A1 (en) | 2015-07-16 | 2017-01-19 | Afton Chemical Corporation | Additives and lubricating oil compositions for improving low speed pre-ignition |
| EP3211062B1 (fr) | 2016-02-29 | 2022-07-27 | TotalEnergies OneTech | Lubrifiant pour moteur marin deux temps |
| US20170292083A1 (en) | 2016-04-06 | 2017-10-12 | Afton Chemical Corporation | TBN and Performance Booster |
| EP3369802B1 (fr) | 2017-03-01 | 2019-07-10 | Infineum International Limited | Améliorations apportées et relatives à des compositions de lubrification |
| KR102617908B1 (ko) | 2017-05-31 | 2023-12-26 | 토탈에너지스 마케팅 써비씨즈 | 폴리아민, 산성 및 붕소 작용기를 포함하는 화합물 및 이의 윤활 첨가제로서의 사용 |
| CN110709493B (zh) | 2017-05-31 | 2022-03-11 | 道达尔销售服务公司 | 包含多胺、酸性官能团和硼官能团的化合物及其作为润滑剂添加剂的用途 |
| SG11202009214RA (en) | 2018-03-23 | 2020-10-29 | Chevron Oronite Co | Composition and method for preventing or reducing low speed pre-ignition in spark-ignited internal combustion engines |
| WO2019229173A1 (fr) | 2018-05-30 | 2019-12-05 | Total Marketing Services | Composé comprenant des fonctions monoammonium quaternaire, acide et bore et son utilisation en tant qu'additif pour lubrifiant |
| CN113227336A (zh) | 2018-11-09 | 2021-08-06 | 道达尔销售服务公司 | 包含多胺、羧酸和硼官能团的化合物及其作为润滑剂添加剂的用途 |
| US20220010231A1 (en) | 2018-11-09 | 2022-01-13 | Total Marketing Services | Compound comprising amine, carboxylate and boron functionalities and its use as a lubricant additive |
| FR3092335B1 (fr) * | 2019-02-04 | 2021-04-30 | Total Marketing Services | Composition lubrifiante pour prévenir le pré-allumage |
| EP3959297B1 (fr) | 2019-04-26 | 2024-06-26 | TotalEnergies OneTech | Composition de lubrifiant et utilisation en tant qu'additif pour lubrifiant de liquides ioniques à base de guanidinium |
| JP7549657B2 (ja) | 2019-11-07 | 2024-09-11 | トタルエナジーズ・ワンテック | ポリアミン官能基、酸性官能基およびホウ素官能基を含む化合物およびその潤滑剤添加剤としての使用 |
| FR3127955B1 (fr) | 2021-10-07 | 2025-05-23 | Totalenergies Marketing Services | Composé spiro comme additif détergent dans des lubrifiants pour moteurs marins |
| FR3127954B1 (fr) | 2021-10-07 | 2023-10-20 | Totalenergies Marketing Services | Composition lubrifiante pour prévenir ou diminuer la combustion anormale dans un moteur |
| FR3127952B1 (fr) | 2021-10-11 | 2025-06-20 | Totalenergies Marketing Services | Carbodiimide comme additif dans des lubrifiants destinés à des systèmes de motorisation pour améliorer la compatibilité avec les élastomères |
-
2021
- 2021-10-07 FR FR2110620A patent/FR3127953B1/fr active Active
-
2022
- 2022-10-06 KR KR1020247015123A patent/KR20240099252A/ko active Pending
- 2022-10-06 WO PCT/EP2022/077850 patent/WO2023057590A1/fr not_active Ceased
- 2022-10-06 EP EP22802028.5A patent/EP4413105A1/fr active Pending
- 2022-10-06 CN CN202280079700.7A patent/CN118339264A/zh active Pending
- 2022-10-06 JP JP2024521018A patent/JP2024536411A/ja active Pending
- 2022-10-06 US US18/699,161 patent/US12460148B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US12460148B2 (en) | 2025-11-04 |
| KR20240099252A (ko) | 2024-06-28 |
| CN118339264A (zh) | 2024-07-12 |
| JP2024536411A (ja) | 2024-10-04 |
| FR3127953B1 (fr) | 2025-07-25 |
| FR3127953A1 (fr) | 2023-04-14 |
| WO2023057590A1 (fr) | 2023-04-13 |
| US20240400928A1 (en) | 2024-12-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP4413104A1 (fr) | Composition lubrifiante pour prévenir ou diminuer la combustion anormale dans un moteur | |
| WO2023057590A1 (fr) | Compose spiro comme additif detergent dans des lubrifiants destines a des systemes de motorisation | |
| EP2245125A1 (fr) | Composition lubrifiante pour moteur quatre temps a bas taux de cendres | |
| CA2955128A1 (fr) | Compositions lubrifiantes pour vehicule a moteur | |
| EP3625315A1 (fr) | Utilisation de compositions lubrifiantes pour ameliorer la proprete d'un moteur de vehicule 4-temps | |
| EP3331973A1 (fr) | Compositions lubrifiantes pour prevenir ou diminuer le pre-allumage dans un moteur | |
| WO2024156810A1 (fr) | Utilisation d'une composition lubrifiante comprenant au moins une huile de base et au moins un alcool gras | |
| WO2023057586A1 (fr) | Composé spiro comme additif détergent dans des lubrifiants pour moteurs marins | |
| EP2935542A1 (fr) | Composition lubrifiante a base d'ether de polyglycerol | |
| EP3237588A1 (fr) | Composition lubrifiante a matériau a changement de phase | |
| EP3134495B1 (fr) | Utilisation d'une composition lubrifiante pour diminuer le cliquetis | |
| WO2019202150A1 (fr) | Composition lubrifiante pour moteurs industriels a potentiel fe amplifie | |
| EP4314214A1 (fr) | Lubrification de moteur de véhicule hybride rechargeable et véhicule hybride comprenant un prolongateur d'autonomie | |
| EP4416251A1 (fr) | Carbodiimide comme additif dans des lubrifiants destinés à des systèmes de motorisation pour ameliorer la compatibilite avec les elastomeres | |
| FR3154120A1 (fr) | Composition lubrifiante comportant une huile lubrifiante re-raffinée et un composé spiro | |
| FR3140887A1 (fr) | Utilisation d’une huile de base spécifique pour réduire les émissions de particules | |
| EP3277738A1 (fr) | Copolymère étoile et son utilisation comme améliorant de viscosité | |
| FR3139343A1 (fr) | Composition lubrifiante avec des propriétés fuel eco améliorées dans les véhicules hybrides | |
| EP3172295A1 (fr) | Composition lubrifiante comprenant un composé anti-cliquetis | |
| FR3011246A1 (fr) | Composition lubrifiante a base de copolymeres ethylene/propylene | |
| FR3158319A1 (fr) | Composition lubrifiante pour prévenir ou diminuer les frottements dans un système mécanique |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
| 17P | Request for examination filed |
Effective date: 20240506 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC ME MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
| REG | Reference to a national code |
Ref country code: HK Ref legal event code: DE Ref document number: 40111986 Country of ref document: HK |
|
| DAV | Request for validation of the european patent (deleted) | ||
| DAX | Request for extension of the european patent (deleted) | ||
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
| 17Q | First examination report despatched |
Effective date: 20250414 |
|
| GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
| INTG | Intention to grant announced |
Effective date: 20260212 |