COMPOSITION OF ADDITIVES AND PERFORMANCE FUEL COMPRISING SUCH A COMPOSITION

专利摘要:
The present invention relates to a fuel additive composition comprising at least a first additive comprising a triazole derivative and a second additive comprising a quaternary ammonium salt. The invention also relates to a diesel fuel comprising such a composition and the use of said fuel to limit deposits in a diesel engine. In particular, the invention relates to the use of the fuel containing the additive composition of the present invention in direct injection diesel engines.
公开号:FR3017876A1
申请号:FR1451437
申请日:2014-02-24
公开日:2015-08-28
发明作者:Geraldine Papin；Julien Gueit
申请人:Total Marketing Services SA；
IPC主号:

专利说明:

[0001] The present invention relates to additive compositions and fuels containing such additive compositions. BACKGROUND OF THE INVENTION The present invention relates to additive compositions and fuels containing such additive compositions. The subject of the present invention relates in particular to additive compositions for diesel and / or biodiesel fuel. Another object of the present invention relates to the use of such fuels in diesel engines to improve their performance, especially in diesel engines with fuel injection system Euro 3 to Euro 6 type.
[0002] Commercial fuels must meet national or supranational specifications (eg EN 590 for diesel fuels in the EU). For commercial fuels, there is no legal requirement for the incorporation of additives. From the point of view of trade, in the field of fuel distribution, "first-price" fuels, with little or no additives, are distinguished from high-quality fuels in which one or more additives are incorporated in order to improve their performance (above beyond regulatory performance). The sulfur content of diesel fuels has been significantly reduced in many countries for environmental reasons, notably to reduce S02 emissions. For example, in Europe, the maximum sulfur content of road diesel fuels is currently 10 ppm. To compensate for the loss of compounds ensuring the lubricating nature of these fuels, many lubricant additives and / or anti-wear and / or friction modifier were introduced into the marketed fuels.
[0003] Their characteristics are widely described in patents EP915944, EP839174 and EP680506. DRAWINGS - FIG. 1 is a photograph of a high pressure direct injection diesel engine injector - FIG. 2 is a photograph of a needle of a direct injection Diesel engine injector, fouled by soap type deposition and or lacquering - Figure 3 is a photograph of a nozzle of a diesel engine injector with indirect injection, fouled by coking type deposit (in English "coking") - Figure 4 is a photograph of a needle of a diesel engine injector with direct injection, fouled by deposition of soap and / or lacquering type (lacquering) As shown in Figures 1 and 2, it was found that during use of certain high quality diesel fuels, deposits 1 appeared on the needles 2 of injector 3 of diesel engine injection systems, especially those of type Euro 3 to Euro 6. Thus, the use of anti-wear additives and / or modifier of rub and / or anti-coking type deposits have sometimes had unsatisfactory lacquering resistance, or even very insufficient. This results in the formation of deposit 1 generally covered by the English term lacquering which will be used in all that follows or by the acronym IDID (Internai Diesel Injector Deposits).
[0004] For the purposes of the present invention, the lacquering phenomenon does not concern deposits which are present outside the injection system 5 or 5 '(FIGS. 1 and 3) and which are related to coking ("coking" in English) at the origin of fouling and partial or total blockage of the injection nozzles 4 or 4 '("nozzle coking" or "fouling" in English).
[0005] Lacquering and coking are two very distinct phenomena, as much because of the causes of these deposits, the conditions of appearance of these deposits and the place where these deposits occur. Coking is a phenomenon that appears only downstream of a Diesel injection system. As shown in FIG. 3, the deposits 5 'formed are characterized in that they consist of pyrolysis of the hydrocarbons entering the combustion chamber and have the appearance of carbonaceous deposits. In the case of diesel direct injection high pressure engines, it has been found that the tendency to coking is much less marked. This coking is conventionally simulated by the standard engine test CEC F098-08 DW10B, especially when the test fuel is contaminated with metallic zinc.
[0006] In the case of indirect injection engines, fuel combustion does not occur directly in the combustion chamber as for direct injection engines. As described for example in US4604102, there is a pre-chamber before the combustion chamber in which the fuel injection is performed. The pressure and temperature in a pre-chamber are lower than that of a combustion chamber of direct injection engines. Under these conditions, the pyrolysis of the fuel produces coal which is deposited on the surface of the nozzles 4 'of the injectors ("throttling diesel nozzle in English" and mouths the orifices 6 of the nozzles 4' (Figure 3). nozzle 4 'exposed to the combustion gases present a risk of depositing coal (coking) .In terms of performance, the phenomenon of coking induces a loss of engine power. Lacquering is a phenomenon that appears only in direct injection diesel engines. and only occurs in the injection system.
[0007] As represented in FIGS. 1 and 2, injectors 3 of direct injection diesel engines comprise a needle 2 whose lifting makes it possible to precisely control the quantity of fuel injected at high pressure directly into the combustion chamber. Lacquering induces the appearance of deposits 1 which appear specifically at the level of the needles 2 of the injectors 3 (Figures 1 and 2). The lacquering phenomenon is related to the formation of soap and / or varnish in the internal parts of the engine injection systems for diesel and / or biodiesel fuels. Lacquering deposit 1 can be located on the end 4 of the needles 2 of injectors 3, both on the head and on the body of the needles 2 of the fuel injection system but also throughout the control system of the Needle lift (valves not shown) of the injection system. This phenomenon is particularly noticeable for engines using diesel fuels of superior quality. When these deposits are present in large quantities, the mobility of the needle 2 of the injector 3 fouled by these deposits 1 is compromised. In addition, unlike coking, lacquering can also cause increased engine noise and sometimes startup problems. Indeed, the parts of the needles 2 fouled by the deposits of soap and / or varnish 1 may stick to the inner walls of the injector 3. The needles 2 are then blocked and the fuel no longer passes. There are usually two types of lacquering deposits: 1. rather whitish and powdery deposits; by analysis, it is found that these deposits consist essentially of sodium soaps (sodium carboxylates, for example) and / or calcium (type 1 deposits); 2. organic deposits comparable to colored varnishes located on the body of the needle (type 2 deposits) With regard to type 1 deposits, the sources of sodium in biogazole type Bx fuels can be multiple: - transesterification catalysts for vegetable oils for the production of esters of (m) ethyl esters of fatty acids such as sodium methanoate; sodium can also come from corrosion inhibitors used for transporting petroleum products in certain pipes, such as sodium nitrite; - Finally, accidental exogenous pollution, for example via water or air, can contribute to the introduction of sodium into fuels (sodium being a very common element). Potential sources of acids in biodiesel-containing fuels can be multiple, for example: o Residual acids in biofuels (see EN14214 which sets a maximum allowable acid level) o Corrosion inhibitors used for the transport of acids petroleum products in certain pipes such as DDSA (dodecenylsuccinic anhydride) or HDSA (hexadecenylsuccinic anhydride) or some of their functional derivatives such as acids. With regard to type 2 organic deposits, some publications state that they may arise in particular from reactions between deposit / dispersant reducing agents used to prevent coking (for example PIBSI-type detergents derived from polyamines) and acids ( which would be present inter alia as impurities of fatty acid esters of biodiesel). In the publication SAE 880493, Reduced Injection Needle Mobility Caused by Lacquer Deposits from Sunflower Oit, the authors M Ziejewski and HJ Goettler describe the phenomenon of lacquering and its adverse consequences for the operation of engines operating with sunflower oils as fuel. In the publication SAE 2008-01-0926, Investigation into the Formation and Prevention of Internal Diesel Injector Deposits, the authors J Ullmann, M Geduldig, H Stutzenberger (Robert Bosch GmbH) and R Caprotti, G Balfour (Infineum) also describe the reactions between acids and deposit / dispersant reducers to explain type 2 deposits. In addition, in the publication SAE International, 2010-01-2242, Internai Injector Deposits in High-Pressure Common Rail Diesel Engines, the authors S. Schwab J. Bennett, S. Dell, J. Galante-Fox, AKulinowski and Keith T. Miller explain that the internal parts of the injectors are usually covered by a slightly colored deposit visible to the naked eye. Their analyzes determined that most of them were sodium salts of alkenyl (hexadecenyl or dodecenyl) succinic acids; sodium from desiccants, caustic water used in refineries, bottom water from tanks or seawater, and succinic diacids being used as corrosion inhibitors or present in multifunctional additive packets. Once formed, these salts are insoluble in diesel fuels with low sulfur content, and as they exist in the form of fine particles, they pass through the diesel fuel filters and are deposited inside the injectors. In this publication, the development of a motor test is described and reproduces the deposits.
[0008] In the publication SAE International, 2010-01-2250, Deposit Control in Modern Diesel Fuel Injection System, the authors, R.Caprotti, N. Bhatti and G. Balfour, also study the same type of internal deposits in injectors and state that the appearance of deposits is not related specifically to a type of fuel (diesel or containing biodiesels) nor to a type of vehicle (light or heavy vehicles) equipped with modern engines (common rail). They show the performance of a new deposit reducer / dispersant, effective on all types of deposits (coking and lacquering). The accumulation of lacquering deposits as described above can lead to the following disadvantages: - a slowing of the fuel injector response, - the sticking of internal parts, which can lead to a loss of control of time injection and the quantity of fuel supplied by injection, - a degradation of the driving pleasure of the vehicle, - variations in power, - an increase in fuel consumption, - an increase in pollutants, - a disturbance of combustion, since the quantity of fuel injected will not be that theoretically expected and the profile of the injection will be different, - an unstable vehicle idle, - an increase in the noise produced by the engine, - a drop in the quality long-term combustion, - a drop in the quality of the spray. In the case where there is a strong depot type lacquering, the vehicle could have great difficulty starting or even not start at all, since the needle for injection would be blocked.
[0009] OBJECT OF THE INVENTION The present invention overcomes the disadvantages mentioned above. In the context of its research, the applicant has shown that the combination of two particular additives made it possible to obtain a surprising synergistic effect, in particular for the control of deposits on the injectors. The present invention provides additive compositions capable of tangibly improving the control of deposits, in particular of the lacquering type of diesel and / or biodiesel fuels. The present invention also provides additive compositions which also improve the control of coking deposits and / or the lubricating properties of the diesel fuel and / or biodiesel. The present invention provides a fuel additive composition comprising at least: - a first additive comprising a triazole derivative of formula (I) below: R1 (I) wherein: R 1 is selected from the group consisting of a hydrogen atom, a linear or branched C 1 -C 8 aliphatic hydrocarbon group, a carboxyl group (-CO 2 H), R2 and R5 are identical or different and represent, independently of each other, a group chosen from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated C1-C33 aliphatic hydrocarbon group, optionally comprising one or more oxygen atoms in the form of carbonyl (-CO-) and / or carboxyl (- CO2H) functions, said R2 and R5 groups possibly forming together a ring of 5 to 8 atoms including the nitrogen to which R2 is bound, it being understood that in this case R2 and R5 then constitute one and the same linear or branched, saturated or unsaturated, C1 to C33 aliphatic hydrocarbon group, optionally substituted with one or more oxygen atoms in the form of a carbonyl function (-CO-) and / or carboxyl (-CO2H),. R3 and R4 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated, cyclic or acyclic aliphatic hydrocarbon group having from 2 to 200 carbon atoms, - a second additive comprising a quaternary ammonium salt obtained by reaction of a nitrogen compound comprising a tertiary amine function with a quaternization agent, said nitrogenous compound being chosen from: a) the product of the reaction of a hydrocarbon-substituted acylating agent and a compound comprising at least one tertiary amine group and a group selected from primary amines, secondary amines and alcohols; b) a product of the Mannich reaction; comprising a tertiary amine group; and c) amines substituted with a polyalkene group having at least one tertiary amine group. Advantageously, the triazole derivative has the formula (I) in which R 3 and R 4 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen atom and a hydrocarbon group aliphatic having a number average molecular weight (Mn) of between 200 and 3000. According to a particular embodiment, the triazole derivative is represented by the following formula (II) and / or (III): wherein R1 , R3 and R4 are as previously defined. According to one development, the triazole derivative is obtained by reacting an aminotriazole of formula (IV) with a diacid of formula (V) and / or a succinic anhydride of the following (VI): (IV) (V) R1, R3 and R4 are as previously defined. In a particular embodiment, the quaternization agent is chosen from the group consisting of dialkyl sulphates, dicarboxylic acid esters and dicarboxylic acid esters. carboxylic acid, alkyl halides, benzyl halides, hydrocarbon carbonates and hydrocarbon epoxides optionally in admixture with an acid, alone or in admixture.
[0010] According to another particular embodiment, the nitrogenous compound comprises a reaction product of a hydrocarbon-substituted acylating agent and an amine of the following formula (VII) or (VIII): R6 R6 R8 N-X Embedded image in which: R 6 and R 7 are identical or different and represent, independently of one another, an alkyl group having 1 to 22 carbon atoms; X is an alkylene group having 1 to 20 carbon atoms, m is an integer of 1 to 5; n is an integer from 0 to 20; and R8 is a hydrogen atom or an alkyl group having 1 to 22 carbon atoms.
[0011] According to another particular embodiment, the additive composition further comprises a third additive comprising at least 50% by weight of a compound A chosen from partial esters of polyols and saturated C4 to C36 aliphatic monocarboxylic hydrocarbons. or unsaturated, linear or branched, cyclic or acyclic, said partial esters can be taken alone or in mixture. In particular, said compound A comprises x ester unit (s), y hydroxyl unit (s) and z ether unit (s), x, y and z being integers such that x varies from 1 to 10, y varies from 1 at 10, and z varies from 0 to 6.
[0012] According to a development, the distribution in ester, hydroxyl and ether units in said compound A is such that x varies from 1 to 4, y varies from 1 to 7 and z varies from 1 to 3. According to one particular embodiment, the compound A is obtained by esterification between: - one or more C4 to C36 fatty acid (s) optionally comprising one or more ethylenic bonds; and a linear or branched, cyclic or acyclic polyol optionally comprising a heterocycle of 5 to 6 atoms, preferably a heterocycle of 4 to 5 carbon atoms and an oxygen atom, substituted by hydroxyl groups.
[0013] According to one development, the fatty acids are chosen from the group consisting of stearic, isostearic, linolenic, oleic, linoleic, behenic, arachidonic, ricinoleic, palmitic, myristic, lauric and capric acids, taken alone or as a mixture.
[0014] According to a particular embodiment, the polyol is chosen from polyols comprising more than three hydroxyl functions and polyols comprising at least one heterocycle of 5 or 6 atoms, preferably heterocycles of 4 to 5 carbon atoms and an oxygen atom. optionally substituted with hydroxyl groups. According to another particular embodiment, the polyol is chosen from polyols comprising at least two heterocycles of 4 or 5 carbon atoms and an oxygen atom, linked by the formation of an acetal bond between a hydroxyl function of each cycle, said heterocycles being optionally substituted with hydroxyl groups. According to one development, the polyol is selected from the group consisting of erythritol, xylitol, arabitol, ribitol, sorbitol, malitol, isomalitol, lactitol, volemitol, mannitol, pentaerythritol, 2-hydroxymethyl-1,3-propandediol, 1,1,1-tri (hydroxymethyl) ethane, trimethylolpropane, sorbitan and carbohydrates such as sucrose, fructose, maltose, glucose and sucrose. According to a particular embodiment, the compound A is chosen from partial esters of sorbitan, preferably sorbitan mono-, di- and tri-esters, taken alone or as a mixture, more preferably the partial esters of sorbitan comprising more than 40% by mass of sorbitan triesters. According to another particular embodiment, the compound A is chosen from monoester (s) and / or diester (s) of polyglycerols having from 2 to 5 glycerol units per molecule. In particular, the compound A is chosen from monoester (s) and / or diester (s) of polyglycerols derived from fatty acid (s), having more than 50% by number of fatty chains comprising between 12 and 24 carbon atoms. preferably, the compound A is chosen from monoester (s) and / or diester (s) of diglycerol and / or triglycerol, more preferentially, from partial esters of diglycerol and / or triglycerol containing at least 50% by weight monoester (s) and / or diester (s) of oleic acid and diglycerol. The object of the present invention also relates to the use of an additive composition according to the present invention, in a diesel fuel having a sulfur content of less than or equal to 500 ppm by weight, preferably comprising a biodiesel. The object of the present invention is also aimed at a diesel fuel having a sulfur content of less than or equal to 500 ppm by mass comprising at least 5 ppm by weight of an additive composition according to the present invention, preferably a fuel comprising up to 30% volume of biodiesel. According to a particular embodiment, the fuel further comprises at least one or more other additives chosen from antioxidants, combustion improvers, corrosion inhibitors, cold-holding additives, dyes, demulsifiers, metal deactivators, defoamers, cetane improvers, lubricant additives, co-solvents and compatibilizers.
[0015] In particular, the mass concentration of each first and second additive and optionally the third additive ranges from 5 to 5000 ppm. The object of the present invention also relates to the use of a diesel fuel according to the present invention in a diesel engine, to improve the performance of said engine, in particular for: - limiting deposits in said diesel engine, - reducing consumption of fuel of said engine ("Fuel Eco" action), - to minimize the loss of power of said engine, maintain the cleanliness of said engine ("keep-clean" action) by limiting the deposits of soap and / or varnish in the internal parts of the engine. injection systems of said engine, and / or - cleaning the fouled internal parts of the injection system of said engine, at least partly removing the deposits of soap and / or varnish in said internal parts (curative action "clean-up" According to a particular embodiment, the engine is a direct injection engine, preferably a high-pressure injection system ("common-rail"). DETAILED DESCRIPTION Other advantages and characteristics The following will become more clearly apparent from the following description. The particular embodiments of the invention are given by way of non-limiting examples. The present invention relates to an additive composition comprising at least a first and a second additive and optionally a third additive. The present invention also relates to the use of such an additive composition in a diesel fuel having a sulfur content of less than or equal to 500 ppm by weight, preferably comprising a biodiesel. First additive The first additive comprises a triazole derivative of formula (I) below: (I) In which: R 1 is chosen from the group consisting of a hydrogen atom, a C 1 to C 8, preferably C 1 to C 4, more preferably C 1 to C 2, linear or branched aliphatic hydrocarbon group and a carboxyl group (-CO 2 H). Preferably, R 1 is a hydrogen atom. . R2 and R5 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen atom and a C1 to C33 aliphatic hydrocarbon group, preferably C1 to C21, linear or branched, saturated or unsaturated, optionally comprising one or more oxygen atoms in the form of carbonyl (-CO-) and / or carboxyl (-CO2H) functions, said R2 and R5 groups possibly forming together a ring of 5 to 8 atoms comprising the nitrogen to which R2 is bonded, it being understood that in this case R2 and R5 then constitute a single, linear or branched, saturated or unsaturated C1 to C33, preferably C1 to C21, aliphatic hydrocarbon group, optionally substituted with one or more oxygen atoms in the form of a carbonyl (-CO-) and / or carboxyl (-CO2H) function. . R3 and R4 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated, cyclic or acyclic aliphatic hydrocarbon group having from 2 to 200 carbon atoms, preferably from 14 to 200 carbon atoms, more preferably from 50 to 170 carbon atoms, even more preferably from 60 to 120 carbon atoms.
[0016] It should be noted that we apply the conventional rules of representation (dotted bond and labile bond) to indicate that the position of the hydrogen atom and the double bond of the triazole ring can change, said formula thus covering both positions possible.
[0017] According to a particular embodiment, the triazole derivative has the formula (I) in which R3 and R4 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen and an aliphatic hydrocarbon group having a number-average molecular weight (Me) of between 200 and 3000, preferably between 400 and 3000, more preferably between 400 and 2500, still more preferably between 400 and 1500 or between 500 and 1500. Said aliphatic hydrocarbon group is preferably a polyisobutylene group (or also called polyisobutene noted PIB) having a number-average molecular weight (Me) of between 200 and 3000, preferably between 400 and 3000, more preferably between 400 and 2500, even more preferably between 400 and 1500 or between 500 and 1500. R3 and R4 preferably represent respectively a hydro atom gene and a PIB group as described above or vice versa. According to another particular embodiment, the triazole derivative is represented by the following formula (II): embedded image in which R 1, R 3 and R 4 are as defined above. According to another particular embodiment, the triazole derivative is represented by the following formula (III): R 3 OH (III) In which R 1, R 3 and R 4 are as defined in the above.
[0018] According to another particular embodiment, the first additive is a mixture of triazole derivatives of formulas (11) and (III) as defined above. The triazole derivative can be in the form of a mixture of derivatives in closed form (II) and open form (III). The mass ratio (11) :( III) in said mixture of triazole derivatives in respectively closed and open form can be between 1: 100 and 100: 1, preferably between 50: 10 and 90: 10, more preferably between 91 : 9 and 99: 1. A first additive comprising less than 10% by weight of triazole derivatives of formula (III) in open form is preferred.
[0019] A triazole derivative or mixture of formula (11) and / or (III) where R1 is a hydrogen atom and R3 and R4 respectively represent a hydrogen atom and a PIB group as described above or conversely (R3 = GDP and R4 = H).
[0020] The triazole derivative may be obtained by any known process, in particular by reacting an aminotriazole of formula (IV) with a diacid of formula (V) and / or a succinic anhydride of formula (VI) below: R 3 OH (IV) ) (V) (VI) wherein R1, R3 and R4 are as defined above. Second additive The second additive comprises a quaternary ammonium salt obtained by reaction of a nitrogen compound comprising a tertiary amine function and a quaternizing agent. Examples of quaternary ammonium salts and process for their preparation are described in US Pat. Nos. 4,225,380, US 3,778,371, US 4,179,559, US 4,326,973, US 4,338,020, US 5,254,418 and WO 2010/1013259, which are incorporated by way of example and / or incorporated by reference into the present application. According to a first particular embodiment of the invention, the nitrogenous compound (a) is chosen from the product of the reaction of a hydrocarbon-substituted acylating agent and a compound comprising at least one tertiary amine group. and a group selected from primary amines, secondary amines or alcohols.
[0021] The nitrogen compound (a) is preferably the product of the reaction of a hydrocarbon-substituted acylating agent and a compound comprising both an oxygen atom or a nitrogen atom capable of condensing with said acylating agent and also a tertiary amine group.
[0022] The acylating agent is advantageously chosen from mono-or polycarboxylic acids substituted with a hydrocarbon group and their derivatives, alone or as a mixture. The acylating agent is, for example, selected from hydrocarbon-substituted succinic, phthalic and propionic acids.
[0023] The hydrocarbon substituent of the acylating agent preferably comprises at least 8, preferably at least 12 carbon atoms, for example between 30 or 50 carbon atoms. The said hydrocarbon substituent may comprise up to about 200 carbon atoms.
[0024] The hydrocarbon substituent of the acylating agent preferably has a number-average molecular weight (Mn) of between 170 and 2800, for example between 250 and 1500, more preferably between 500 and 1500, and even more preferably between 500 to 1100. A range of Mn value between 700 and 1300 is particularly preferred, for example from 700 to 1000.30. By way of example of hydrocarbon groups which substitute the acylating agent, mention may be made of n-octyl groups, n-decyl, n-dodecyl, tetrapropenyl, noctadecyl, oleyl, octadecyl or triacontyl.
[0025] The hydrocarbon substituent of the acylating agent can be obtained from homo- or inter-polymers (for example copolymers, terpolymers) of mono-and di-olefins having from 2 to 10 carbon atoms, by example from ethylene, propylene, 1-butene, isobutene, butadiene, isoprene, 1-hexene or 1-octene. Preferably, these olefins are 1-mono-olefins.
[0026] The hydrocarbon substituent of the acylating agent may also be derivatives of halogenated analogs (for example chlorinated or brominated) of these homo- or inter-polymers.
[0027] Alternatively, the hydrocarbon substituent of the acylating agent may be obtained from other sources, for example from high molecular weight (eg 1-tetracontene) alkenes monomers and their chlorinated or hydrochlorinated aliphatic petroleum fractions, for example paraffin waxes, their cracked, chlorinated and / or hydrochlorinated analogs, white oils, synthetic alkenes, for example produced by the Ziegler-Natta process (for example polyethylene greases). ) and other sources known to those skilled in the art. Any unsaturation in the hydrocarbon group of the acylating agent may also be reduced or eliminated by hydrogenation according to any known method.
[0028] By "hydrocarbon" group is meant any group having a carbon atom directly attached to the remainder of the molecule and having mainly an aliphatic hydrocarbon character.
[0029] Hydrocarbon groups according to the invention may also contain non-hydrocarbon groups. For example, they may contain up to one non-hydrocarbon moiety per ten carbon atoms provided that the non-hydrocarbon moiety does not significantly alter the predominantly hydrocarbon character of the moiety. Examples of such groups well known to those skilled in the art include hydroxyl groups, halogens (in particular chloro- and fluoro- groups), alkoxy, alkylmercapto and alkylsulphoxy groups. Hydrocarbon substituents which do not contain such non-hydrocarbon groups and which have a purely aliphatic hydrocarbon character will nevertheless be preferred. The hydrocarbon substituent of the acylating agent is preferably substantially saturated, i.e. it does not contain more than one unsaturated carbon-carbon bond for each ten carbon-carbon single bonds. present. The hydrocarbon substituent of the acylating agent preferably contains not more than one non-aromatic carbon-carbon unsaturated bond at any of the 50 carbon-carbon bonds present.
[0030] According to a particular preferred embodiment, the hydrocarbon substituent of the acylating agent is preferably chosen from the polyisobutenes known in the prior art. Advantageously, the acylation agent substituted with a hydrocarbyl group is a polyisobutenyl succinic anhydride (PIBSA).
[0031] The preparation of polyisobutenyl succinic anhydrides (PIBSA) is widely described in the literature. By way of example, mention may be made of processes comprising the reaction between polyisobutenes (PIB) and maleic anhydride described in documents US Pat. No. 3,316,773 and US Pat. No. 3,018,250, or the process comprising the reaction of a halogenated polyisobutene (PIB), in particular chlorinated polyisobutene (PIB). with maleic anhydride (US3172892).
[0032] Alternatively, the polyisobutenyl succinic anhydride can be prepared by mixing a polyolefin with maleic anhydride and then passing chlorine through the mixture (GB949981).
[0033] In particular, the so-called highly reactive polyisobutenes (PIB) will be used. Highly reactive polyisobutenes (PIB) are polyisobutenes (PIB) in which at least 50%, preferably at least 70% or more, of the terminal olefinic double bonds are of the vinylidene type as described in EP0565285. In particular, the preferred PIBs are those having more than 80 mol% and up to 100 mol% of vinylidene end groups as described in document EP1344785. Other hydrocarbon groups comprising an internal olefin, for example, such as those described in application WO2007 / 015080 may also be used. The term internal olefin is understood to mean any olefin containing mainly a non-alpha double bond, which is a beta olefin or of higher position. Preferably, these materials are essentially beta-olefins or higher-position olefins, for example containing less than 10% by weight alpha-olefin, advantageously less than 5% by weight or less than 2% by weight. Internal olefins can be prepared by isomerization of alpha-olefins according to any known method. The compound comprising both an oxygen atom or a nitrogen atom capable of condensing with the acylating agent and a tertiary amine group may, for example, be selected from the group consisting of: N, N- dimethylaminopropylamine, N, N-diethylaminopropylamine, N, N-dimethylaminoethylamine. Said compound may be further selected from heterocyclic compounds substituted with alkylamines such as 1- (3-aminopropyl) imidazole and 4- (3-aminopropyl) morpholine, 1- (2-aminoethyl) piperidine, 3,3 diamino-N-methyldipropylamine, and 3'-bisamino (N, N-dimethylpropylamine).
[0034] The compound comprising both an oxygen atom or a nitrogen atom capable of condensing with the acylating agent and a tertiary amine group may also be selected from alkanolamines, including, but not limited to , triethanolamine, trimethanolamine, N, N-dimethylaminopropanol, N, N-dimethylaminoethanol, N, N-diethylaminopropanol, N, N-diethylaminoethanol, N, N-diethylaminobutanol, N, N, N-tris (hydroxyethyl ) amine, N, N, N-tris (hydroxymethyl) amine, N, N, N-tris (aminoethyl) amine, N, N-dibutylaminopropylamine and N, N, N'-trimethyl-N'-hydroxyethyl bis-aminoethyl ether, N, N-bis (3-dimethylaminopropyl) -N-isopropanolamine, N- (3-dimethylaminopropyl) -N, N-diisopropanolamine, N '- (3- (Dimethylamino) propyl) -N N, N-dimethyl-1,3-propanediamine; 2- (2-dimethylaminoethoxy) ethanol and N, N, N'-trimethylaminoethylethanolamine. According to a particular embodiment, the nitrogen compound (a) comprises a reaction product of a hydrocarbon-substituted acylating agent and an amine of the following formula (VIII) or (IX): R6 R6 / Wherein: R6 and R7 are the same or different and represent, independently of one another, an amount of at least one of R6 and R7; alkyl group having 1 to 22 carbon atoms; X is an alkylene group having 1 to 20 carbon atoms; m is an integer from 1 to 5; n is an integer from 0 to 20; and R8 is a hydrogen atom or an alkyl group of C1 to C22.
[0035] When the nitrogen compound (a) comprises an amine of formula (VII), R 8 is advantageously a hydrogen atom or a C 1 to C 16 alkyl group, preferably a C 1 to C 10 alkyl group, more preferably still an alkyl group. C1 to C6. R8 may, for example, be selected from the group consisting of hydrogen, methyl, ethyl, propyl, butyl and their isomers. Preferably R8 is a hydrogen atom. When the nitrogen compound (a) comprises an amine of formula (VIII), m preferably of 2 or 3, more preferably of 2; n is preferably an integer between 0 to 15, more preferably between 0 to 10, even more preferably between 0 to 5. Advantageously, n is 0 and the compound of formula (VIII) is an alcohol.
[0036] According to a preferred embodiment, the nitrogen compound (a) is the product of the reaction of the acylation agent substituted with a hydrocarbon group and the diamine of formula (VII). R6 and R7 may represent, independently of one another, a C1 to C16 alkyl group, preferably a C1 to C10 alkyl group to an alkyl group. R6 and R7 may represent, independently of one another, a methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl or isomeric group thereof. Advantageously, R6 and R7 represent, independently of one another, a C1 to C4 group, preferably a methyl group.
[0037] X represents, preferably, an alkylene group having 1 to 16 carbon atoms, preferably 1 to 12 carbon atoms, more preferably 1 to 8 carbon atoms, for example 2 to 6 carbon atoms or 2 to 6 carbon atoms; 5 carbon atoms. X is advantageously an ethylene, propylene or butylene group, in particular a propylene group. The quaternary ammonium salt of the second additive may, for example, be obtained according to the preparation process described in international application WO2006 / 135881.
[0038] According to a preferred variant, the nitrogen compound (a) is the reaction product of a succinic acid derivative substituted with a hydrocarbon group, preferably a polyisobutenyl succinic anhydride, and an alcohol or an amine also comprising a tertiary amine group.
[0039] The succinic acid derivative substituted with a hydrocarbon group reacts with the amine also comprising a tertiary amine group under certain conditions to form a succinimide (closed form). According to one variant, the reaction of the succinic acid derivative and the amine may, under certain conditions, lead to a succinamide, that is to say a compound comprising an amide group and a carboxylic acid group (open form). According to another variant, an alcohol also comprising a tertiary amine group reacts with the succinic acid derivative to form an ester. This ester molecule also comprises a carboxyl group -CO2H free (open form). Thus, in some embodiments, the nitrogen compound (a) may be the reaction product of a succinic acid derivative and an amine or an alcohol which is an ester or an amide and which further comprises also a group carboxyl - CO 2 H unreacted (open form). According to a second particular embodiment of the invention, the nitrogenous compound (b) is chosen from a product of the Mannich reaction comprising a tertiary amine group.
[0040] The preparation of quaternary ammonium salts formed from a nitrogen compound, in particular from nitrogenous compound (b), is described, for example, in document US2008 / 0052985.
[0041] The product of the Mannich reaction comprising a tertiary amine group is prepared by reacting a phenol substituted with a hydrocarbon group, an aldehyde and an amine. The hydrocarbon substituent of said phenol may contain from 6 to 400 carbon atoms, advantageously from 30 to 180 carbon atoms, for example from 10 to 110, or from 40 to 110 carbon atoms.
[0042] The hydrocarbon substituent of said phenol may be derived from an olefin or a polyolefin. By way of example, mention may be made of alpha-olefins such as n-1-decene. The polyolefins forming the hydrocarbon substituent of the phenol can be prepared by polymerization of olefin monomers according to any known polymerization process. Advantageously, the polyolefins are chosen from polyisobutylenes having a number-average molecular weight (Mn) of between 400 to 3000, preferably between 400 to 2500, more preferably between 400 and 1500 or between 500 and 1500.
[0043] The hydrocarbon-substituted phenol may be prepared by alkylating phenol with an olefin or polyolefin described above, such as polyisobutylene or polypropylene, using conventional alkylation methods.
[0044] According to one variant, the phenol may be substituted with one or more low molecular weight alkyl groups, for example a phenol bearing one or more alkyl chains of less than 28 carbon atoms, preferably of less than 24 carbon atoms, more preferably of less than 20 carbon atoms, more preferably less than 18 carbon atoms, still more preferably 16 carbon atoms and even more preferably 14 carbon atoms.
[0045] A monoalkyl phenol preferably having from 4 to 20 carbon atoms, preferably from 6 to 18, more preferably from 8 to 16, even more preferably from 10 to 14 carbon atoms, for example a phenol substituted by a group, is preferred. C12 alkyl. The aldehyde used to form the product of the Mannich reaction may comprise from 1 to 10 carbon atoms, and is generally formaldehyde or its reactive equivalents such as formalin (methyl alcohol and formaldehyde) or paraformaldehyde. The amine used to form the product of the Mannich reaction may be a monoamine or a polyamine. By way of nonlimiting examples, mention may be made, as monoamines, of ethylamine, dimethylamine, diethylamine, n-butylamine, dibutylamine, allylamine, isobutylamine, cocoamine, stearylamine, laurylamine, methyllaurylamine, oleylamine, N-methyloctylamine, dodecylamine, diethanolamine, morpholine and octadecylamine.
[0046] The polyamines are chosen from compounds comprising two or more amine groups. By way of non-limiting examples, mention may be made, as polyamines, of polyalkylene polyamines in which the alkylene group has, for example, from 1 to 6, preferably from 1 to 4, more preferably from 2 to 3 carbon atoms. Preferred polyamines are polyethylene polyamines.
[0047] The polyamine may comprise from 2 to 15 nitrogen atoms, preferably from 2 to 10 nitrogen atoms, preferably 2 to 8 nitrogen atoms. In a preferred embodiment, the amine used to form the Mannich reaction product comprises a diamine, preferably, which comprises a primary or secondary amine function participating in the Mannich reaction and a tertiary amine.
[0048] In a particular embodiment, the nitrogenous compound (b) comprises the product obtained directly by Mannich reaction, and comprising a tertiary amine. For example, the amine comprises a single primary or secondary amine function which is involved in the Mannich reaction and a tertiary amine capable of being quaternized. According to one variant, the amine comprises a primary or secondary amine capable of taking part in the Mannich reaction, and also a tertiary amine capable of being quaternized. According to another variant, the nitrogenous compound (b) can be obtained by a Mannich reaction and then subjected to a reaction which makes it possible to obtain a tertiary amine, for example a process employing an intermediate compound comprising a secondary amine and obtained by Mannich reaction which is then modified for example alkylation to give a secondary amine. According to a third particular embodiment of the invention, the nitrogen compound (c) is chosen from amines substituted with a polyalkene (also called polyalkylene) group having at least one tertiary amine group. The preparation of quaternary ammonium salts formed from a nitrogen compound (c) is, for example, described in US2008 / 0113890.
[0049] The amines substituted with a polyalkene group having at least one tertiary amine group may be derived from polyolefin and amine, for example ammonia, momoamines, polyamines, alone or in combination. Said amines can be prepared according to any known process, for example those described in document US2008 / 0113890.30. By way of nonlimiting examples, mention may be made of the reaction of a halogenated olefinic polymer with an amine; reacting a hydroformylated olefin with a polyamine followed by hydrogenation of the reaction product; converting a polyalkene to the corresponding epoxide followed by conversion of the epoxide to polyalkene amine by reductive amination; hydrogenation of a 13-aminonitrile; and hydroformylating a polybutene or polyisobutylene in the presence of a catalyst, CO and H 2 at elevated pressure and temperatures. The olefinic monomers from which the olefinic polymers are derived include the polymerizable olefinic monomers characterized by the presence of one or more ethylenic unsaturations, for example ethylene, propylene, 1-butene, isobutene, octane, 1,3-butadiene and isoprene. The olefinic monomers are generally polymerizable terminal olefins. However, polymerizable internal olefinic monomers can also be used to form the polyalkenes. By way of non-limiting examples, the terminal and internal olefinic monomers which can be used to prepare the polyalkenes by any known method are: ethylene; propylene; butenes, including 1-butene, 2-butene and isobutylene; 1-pentene; 1-hexene; 1-heptene; 1-octene; 1-nonene; 1-decene; 2-pentene; propylene tetramer; diisobutylene; isobutylene trimer; 1,2-butadiene; 1,3-butadiene; 1,2-pentadiene; 1,3-pentadiene; 1,4-pentadiene; isoprene; 5-hexadiene, 2-methyl-5-propyl-1-hexene; 3-pentene; 4-octene and 3,3-dimethyl-1-pentene.
[0050] The amines substituted by derivatives of polyisobutylene will preferably be chosen. The amines used to prepare the amines substituted with a polyalkene group may be chosen from ammonia, monoamines, polyamines alone or as mixtures, including mixtures of different monoamines, mixtures of different polyamines, and mixtures of monoamines and polyamines (including diamines). Said amines include aliphatic, aromatic, heterocyclic hydrocarbons and carbocyclic amines.
[0051] The monomers and polyamines advantageously comprise at least one primary or secondary amine. The monoamines are generally substituted with a hydrocarbon group having 1 to about 50 carbon atoms, preferably 1 to 30 carbon atoms. Saturated aliphatic hydrocarbon substituents are particularly preferred. By way of example, mention may be made of methylamine, ethylamine, diethylamine, 2-ethylhexylamine, di- (2-ethylhexyl) amine, n-butylamine, di-n-butylamine and allylamine. isobutylamine, cocoamine, stearylamine, laurylamine, methyllaurylamine and oleylamine. Aromatic monoamines include monoamines in which a carbon atom having an aromatic ring structure is attached directly to the amine nitrogen. Examples of aromatic monoamines include aniline, di- (para-methylphenyl) amine, naphthylamine and N- (n-butyl) aniline. Examples of aromatic monoamines substituted with aliphatic, cycloaliphatic and heterocyclic hydrocarbon moieties include para-dodecylaniline, cyclohexyl-naphthylamine and thienylaniline, respectively. Monoamines according to the present invention also include hydroxyamines. For example, ethanolamine, di-3-propanolamine, 4-hydroxybutylamine, diethanolamine and N-methyl-2-hydroxypropylamine can be mentioned. The polyamines can also be chosen from substituted amines. by polyalkene groups. The polyamine may be aliphatic, cycloaliphatic, heterocyclic or aromatic. By way of example, mention may be made of alkylene polyamines, hydroxy-substituted polyamines, arylpolyamines and heterocyclic polyamines. Ethylenic polyamines are preferred for reasons of cost and efficiency. Hydroxyl substituted polyamines include hydroxyalkylated alkene polyamines having one or more hydroxyalkyl substituents on the nitrogen atoms and which may be prepared by reacting the alkene polyamines with one or more alkene oxides. By way of example, mention may be made of N- (2-hydroxyethyl) ethylenediamine, N, N-bis (2-hydroxyethyl) ethylene diamine, 1- (2-hydroxyethyl) p-piperazine, and monohydroxypropyl-diethylene glycol. triamine, hydroxypropyl-tetraethylenepentamine and N- (3-hydroxybutyl) tetramethylenediamine. The arylpolyamines are analogous to the aromatic monoamines described above with the exception of the presence in their structure of another amino nitrogen. For example, N, N'-di-n-butyl-para-phenylenediamine and bis- (para-aminophenyl) methane may be mentioned. Heterocyclic mono- and polyamines will be known to those skilled in the art. Examples are N-aminopropylmorpholine, N-aminoethylpiperazine, and N, N'-diaminoethylpiperazine. The heterocyclic hydroxy-polyamines can also be used, for example N- (2-hydroxyethyl) cyclohexylamine, 3-hydroxycyclopentylamine, parahydroxyaniline and N-hydroxyethlpiperazine. Examples of amines substituted with polyalkene groups may include: polypropylene amine, polybutene amine, N, N-dimethyl-polyisobutylene amine, N-polybutene-morpholine, N-polybutene-ethylenediamine, N-polypropylene trimethylenediamine N-polybutene-diethylene triamine, N ', N'-polybutene-tetraethylenepentamine and N, N-dimethyl-N-polypropylene-1,3-propylenediamine. The number average molecular weight (Me) of the polyalkene-substituted amines can range from 500 to 5000, preferably from 500 to 3000, for example from 1000 to 1500. All the polyalkene-substituted amines described above which are primary amines or secondary, can be alkylated to form tertiary amine functions using alkylating agents by any known method. The quaternary ammonium salt of the second additive according to the present invention is directly obtained by reaction between the nitrogen compound described above comprising a tertiary amine function and a quaternization agent.
[0052] According to a particular embodiment, the quaternarization agent is chosen from the group consisting of dialkyl sulphates, carboxylic acid esters; alkyl halides, benzyl halides, hydrocarbon carbonates, and hydrocarbon epoxides optionally in admixture with an acid, alone or as a mixture. For fuel applications, it is often desirable to reduce the content of halogen, sulfur and phosphorus-containing compounds.
[0053] Thus, if a quaternizing agent containing such an element is used, it may be advantageous to perform a subsequent reaction to exchange the counterion. For example, a quaternary ammonium salt formed by reaction with an alkyl halide can then be reacted with sodium hydroxide and the sodium halide salt removed by filtration. The quaternizing agent can include halides such as chloride, iodide or bromide; hydroxides; sulfonates; bisulphites; alkyl sulphates such as dimethyl sulphate; sulfones; phosphates; C1-C12 alkylphosphates; C1-C12 dialkylphosphates; borates; C1-C12 alkylborates; nitrites; nitrates; carbonates; bicarbonates; alkanoates; the C1-C12 0,0-dialkyldithiophosphates, alone or as a mixture. According to one particular embodiment, the quaternizing agent may be derived from dialkyl sulphates such as dimethyl sulphate, N-oxides, sulphones such as propane and butanesulfone, alkyl halides, acyl or aralkyl such as methyl and ethyl chloride, bromide, iodide or benzyl chloride, and hydrocarbon carbonates (or alkylcarbonates). If the acyl halide is benzyl chloride, the aromatic ring is optionally substituted with one or more alkyl or alkenyl groups. The hydrocarbon (alkyl) groups of the hydrocarbon carbonates may contain from 1 to 50, from 1 to 20, from 1 to 10 or 1 to 5 carbon atoms per group. According to a particular embodiment, the hydrocarbon carbonates contain two hydrocarbon groups which may be identical or different. As an example of hydrocarbon carbonates, mention may be made of dimethyl or diethyl carbonate. According to a particular embodiment, the quaternizing agent is chosen from hydrocarbon epoxides represented by the following formula (IX): R 9 R 11 (IX) in which R 9, R 10, R 11 and R 12 may be identical or different and independently represent a hydrogen atom or a C1-050 hydrocarbon group. By way of non-limiting example, mention may be made of styrene oxide, ethylene oxide, propylene oxide, butylene oxide, stilbene oxide and C 1 -C 50 epoxides. Styrene oxide is particularly preferred.
[0054] Typically, such hydrocarbon epoxides are used as a quaternization agent in combination with an acid, for example with acetic acid. Nevertheless, in the particular embodiment described above involving the nitrogenous compound (a) consisting of a substituted succinamide comprising both an amide or ester function and a carboxylic acid function (open form), the hydrocarbon epoxide may be used alone as the quaternarization agent without additional acid. Without being bound by this hypothesis, it would seem that the presence of the carboxylic acid function in the molecule promotes the formation of the quaternary ammonium salt.
[0055] In such a particular embodiment not using additional acid, a protic solvent is used for the preparation of the quaternary ammonium salt. For example, protic solvents such as water, alcohols (including polyhydric alcohols) can be used alone or in mixture. Preferred protic solvents have a dielectric constant greater than 9. Suitable quaternary ammonium salts prepared from amides or esters and succinic acid derivatives are described in WO2010 / 132259. According to a particular embodiment, the quaternarization agent comprises a compound of formula (X): R 14 (X) R 10 / in which R 13 is an optionally substituted alkyl, alkenyl, aryl and aralkyl group, and R 14 is a grouping C1 to C22 alkyl, aryl or alkylaryl.
[0056] The compound of formula (X) is a carboxylic acid ester capable of reacting with a tertiary amine to form a quaternary ammonium salt. Compounds of formula (X) are selected, for example from carboxylic acid esters having a pKa of 3.5 or less. The compound of formula (X) is preferably selected from esters of substituted aromatic carboxylic acid, hydroxycarboxylic acid and polycarboxylic acid. According to a particular embodiment, the ester is a substituted aromatic carboxylic acid ester of formula (X) in which R 13 is a substituted aryl group. Preferably, R 13 is a substituted aryl group having 6 to 10 carbon atoms, preferably a phenyl or naphthyl group, more preferably a phenyl group. R13 is advantageously substituted with one or more groups chosen from carboalkoxy, nitro, cyano, hydroxy, SR15 and NR15 R16 radicals. Each of the groups R15 and R16 may be a hydrogen atom or an optionally substituted alkyl, alkenyl, aryl or carboalkoxy group. Each of the groups R15 and R16 preferably represents the hydrogen atom or an optionally substituted C1-C22 alkyl group, preferably the hydrogen atom or a C1-C16 alkyl group, more preferentially the at least one hydrogen atom. hydrogen or a C1 to C10 alkyl group, still more preferably a hydrogen atom or a C1 to C4 alkyl group. R15 is preferably a hydrogen atom and R16 a hydrogen atom or a C1 to C4 group. Advantageously, R15 and R16 are both a hydrogen atom.
[0057] According to a particular embodiment, R 13 is an aryl group substituted by one or more groups chosen from hydroxyl, carboalkoxy, nitro, cyano and NH 2 radicals. R13 may be a polysubstituted aryl group, for example trihydroxyphenyl. Advantageously, R13 is a monosubstituted aryl group, preferably substituted in ortho. R13 is, for example, substituted with a group selected from OH, NH2, NO2 or COOMe, preferably OH or NH2. R13 is preferably a hydroxy-aryl group, especially 2-hydroxyphenyl. According to a particular embodiment, R14 is an alkyl or alkylaryl group. R14 may be a C1 to C16, preferably C1 to C10, advantageously C1 to C8, alkyl group. R14 may be a C1 to C16 alkylaryl group, preferably a C1 to C10, advantageously a C1 to C8 group. R14 may for example be selected from methyl, ethyl, propyl, butyl, pentyl, benzyl groups or their isomers. Preferably, R14 is a benzyl or methyl group, more preferably methyl. A particularly preferred compound of formula (X) is methyl salicylate. According to a particular embodiment, the compound of formula (X) is an ester of an α-hydroxycarboxylic acid of the following formula: R 17 R 18 COOR 14 OH In which R 17 and R 18 are identical or different and are independently selected from the group consisting of in the hydrogen atom, the alkyl, alkenyl, aryl or aralkyl groups. Such compounds are for example described in EP 1254889. Examples of compounds of formula (X) in which R 13 CO 2 is the residue of an α-hydroxycarboxylic acid include methyl, ethyl, propyl, butyl, pentyl and the like. -, hexyl-, phenyl-, benzyl- or allyl-2-hydroxy-isobutyric acid esters; 2-hydroxy-2-methylbutyric acid methyl-, ethyl-, propyl-, butyl-, pentyl-, hexyl-, benzyl-, phenyl or allyl-esters; methyl-, ethyl-, propyl-, butyl- 2-hydroxy-2-ethylbutyric acid, pentyl-, hexyl-, benzyl-, phenyl- or allyl-esters; methyl-, ethyl-, propyl-, butyl-, pentyl-, hexyl-, benzyl-, phenyl or allyl-lactic acid esters and methyl-, ethyl-, propyl-, butyl-, pentyl-, hexyl-, allyl-, benzyl or phenyl-glycolic acid esters.For the above, the preferred compound is methyl-2-hydroxyisobutyrate.
[0058] According to a particular embodiment, the compound of formula (X) is an ester of a polycarboxylic acid comprising dicarboxylic acids and carboxylic acids having more than two acid functions. The carboxylic functions are preferably all in esterified form. The preferred esters are C1-C4 alkyl esters. The compound of formula (X) may be selected from oxalic acid diesters, phthalic acid diesters, maleic acid diesters, malonic acid diesters or citric acid diesters. Preferably, the compound of formula (X) is dimethyl oxalate. According to a preferred variant, the compound of formula (X) is a carboxylic acid ester having a pKa of less than 3.5. For cases where the compound comprises more than one acid group, reference is made to the first dissociation constant.
[0059] The compound of formula (X) may be chosen from one or more carboxylic acid esters chosen from oxalic acid, phthalic acid, salicylic acid, maleic acid, malonic acid and citric acid. , nitrobenzoic acid, aminobenzoic acid and 2,4,6-trihydroxybenzoic acid. Preferred compounds of formula (X) are dimethyl oxalate, methyl 2-nitrobenzoate and methyl salicylate. According to a particularly preferred embodiment, the quaternary ammonium salt according to the invention is formed by reacting methyl 2-hydroxybenzoate or styrene oxide with the product of the reaction of a polyisobutenyl succinic anhydride whose polyisobutylene (PIB) group has a number average molecular weight (Mn) of between 700 and 1000 and dimethylaminopropylamine. According to a particular preferred embodiment, the additive composition comprises the first additive as described above preferably comprising a triazole derivative of formula (II) and / or (III) and the second additive comprising a salt of quaternary ammonium obtained from the nitrogen compound (a) described above.
[0060] Third additive According to a particular embodiment, the additive composition described above may further comprise a third additive. The third additive comprises at least 50% by weight of a compound A chosen from partial esters of polyols and of C4 to C36, preferably C12-C24, more preferably C16-C20, monocarboxylic aliphatic hydrocarbons, which are saturated or unsaturated. , linear or branched, cyclic or acyclic, said partial esters can be taken alone or in mixture. Compound A preferably comprises x ester units, y hydroxyl units and z ether units, x, y and z being integers such that x varies from 1 to 10, y ranges from 1 to 10, and z varies from 0. to 6. According to a particular embodiment, x varies from 1 to 10, y varies from 3 to 10, and z varies from 0 to 6.
[0061] According to another particular embodiment x varies from 1 to 4, y varies from there 7 and z varies from 1 to 3. Advantageously, x varies from 2 to 4. The synthesis of partial esters of polyols is known per se; they may for example be prepared by esterification of fatty acid (s) and linear and / or branched polyols optionally comprising (hetero) rings of 5 to 6 atoms supporting hydroxyl functions. Generally this type of synthesis leads to a mixture of mono-, di-, tri- and optionally tetra-esters as well as small amounts of unreacted fatty acid (s) and polyols.
[0062] According to a particular embodiment, the compound A is obtained by esterification of one or more fatty acid (s) C4 to C36, preferably C10-C24, more preferably C12-C24, optionally comprising one or more bonds ethylene, and a linear or branched, cyclic or acyclic polyol optionally comprising a heterocycle of 5 to 6 atoms, preferably a heterocycle of 4 to 5 carbon atoms and an oxygen atom, substituted by hydroxyl groups. The fatty acids are advantageously chosen from the group consisting of stearic, isostearic, linolenic, oleic, linoleic, behenic, arachidonic, ricinoleic, palmitic, myristic, lauric and capric acids, taken alone or as a mixture. The fatty acids can come from the transesterification or saponification of vegetable oils and / or animal fats. Preferred vegetable oils and / or animal fats will be selected according to their concentration of oleic acid. For example, see Table 6.21 in Chapter 6 of the book Fuels & Engines by J.C. Guibet and E. Faure, 2007 edition, which lists the compositions of several vegetable oils and animal fats.
[0063] The fatty acids may also be derived from tall oil fatty acids (Tall Oil Fatty Acids) which comprise a major amount of fatty acids, typically greater than or equal to 90% by mass, as well as resin acids and unsaponifiables in a minor amount. , ie in quantities generally less than 10%.
[0064] The polyol will preferably be chosen from linear or branched polyols comprising more than three hydroxyl functions and polyols comprising at least one ring of 5 or 6 atoms, preferably a heterocycle of 4 to 5 carbon atoms and an atom of oxygen, optionally substituted by hydroxyl groups, taken alone or as a mixture. According to a preferred variant, the polyol is chosen from polyols comprising at least one ring of 5 or 6 atoms, preferably a heterocycle of 4 to 5 carbon atoms and an oxygen atom, optionally substituted with hydroxyl groups, taken alone. or in mixture. According to another variant, the polyol is chosen from polyols comprising at least two heterocycles of 4 or 5 carbon atoms and an oxygen atom, linked by the formation of an acetal bond between a hydroxyl function of each ring, said heterocycles being optionally substituted with hydroxyl groups. The polyol is, in particular, chosen from the group consisting of erythritol, xylitol, arabitol, ribitol, sorbitol, malitol, isomalitol, lactitol, volemitol, mannitol, pentaerythritol, 2-hydroxymethyl-1,3-propandediol, 1,1,1-tri (hydroxymethyl) ethane, trimethylolpropane, sorbitan and carbohydrates such as sucrose, fructose, maltose, glucose and sucrose, preferably sorbitan.
[0065] According to a particular embodiment, the compound A is chosen from partial esters of sorbitan, preferably sorbitan di-, mono- and tri-esters, taken alone or as a mixture. According to one variant, the compound A is chosen from partial esters of sorbitan comprising more than 40% by mass of sorbitan triesters, preferably more than 50% by mass.
[0066] According to another variant, the compound A chosen from partial esters of sorbitan comprising more than 20% by weight of sorbitan monoesters and / or more than 20% by weight of sorbitan diesters, preferably more than 20% by weight of sorbitan monoesters and / or more than 30% by weight of sorbitan diesters, more preferably more than 25% by weight of sorbitan monoesters and / or more than 35% by weight of sorbitan diesters. According to another particular embodiment, the compound A is chosen from monoester (s) and / or diester (s) of polyglycerols derived from fatty acid (s), having more than 50% by number of fatty chains comprising between 12 and 24 carbon atoms. Such polyglycerols have been described in WO2013 / 120985 and are exemplified and / or incorporated by reference in the present application.
[0067] Compound A is preferably chosen from monoester (s) and / or diester (s) of diglycerol and / or triglycerol. In particular, the partial esters of diglycerol and / or triglycerol comprise at least 50% by weight of monoester (s) and / or diester (s) of oleic acid and diglycerol, and thus of mono-oleate (s) of diglycerol. (DGMO) and / or dioleate (s) diglycerol (DGDO) is at least 50% by weight of mono- and / or diester (s) of oleic acid and triglycerol, or at least 50% by weight of mono- and / or diester (s) of oleic acid and diglycerol and / or triglycerol.
[0068] According to a particular embodiment, each of the first, second and third additives consist solely of their respective active ingredient, namely the triazole derivative for the first additive, the quaternary ammonium salt for the second additive and the compound A for the second additive. the third additive.
[0069] According to a particular embodiment, the additive composition comprises the first additive, the quaternary ammonium salt obtained from the nitrogenous compound (a) and a compound A chosen from the partial esters of sorbitan previously described, preferably a triester. of sorbitan. According to one variant, the additive composition comprises the first additive, the quaternary ammonium salt obtained from the nitrogenous compound (a) and a compound A chosen from monoesters and / or diesters of polyglycerols derived from fatty acids such as previously described. According to another particular embodiment, the additive composition comprises the first additive, the quaternary ammonium salt obtained from the nitrogenous compound (b) and a compound A chosen from the partial esters of sorbitan previously described, preferably a triester of sorbitan. According to one variant, the additive composition comprises the first additive, the quaternary ammonium salt obtained from the nitrogenous compound (b) and a compound A chosen from monoesters and / or diesters of polyglycerols derived from fatty acids such as previously described. According to another particular embodiment, the additive composition comprises the first additive, the quaternary ammonium salt obtained from the nitrogenous compound (c) and a compound A chosen from the partial esters of sorbitan previously described, preferably a triester of sorbitan. According to one variant, the additive composition comprises the first additive, the quaternary ammonium salt obtained from the nitrogenous compound (c) and a compound A chosen from monoesters and / or diesters of polyglycerols derived from fatty acids such as previously described. The additive composition described above may also comprise one or more other conventional additives. By way of example, mention may be made of antioxidants, combustion improvers, corrosion inhibitors, cold-holding additives, dyes, demulsifiers, metal deactivators, anti-foaming agents, agents and the like. improving the cetane number, lubricity additives, co-solvents and compatibilizers.
[0070] In a non-exhaustive manner, the other functional additive (s) may be chosen from: combustion enhancing additives; mention may be made of procetane additives, in particular (but not limited to) selected from alkyl nitrates, preferably 2-ethyl hexyl nitrate, aryl peroxides, preferably benzyl peroxide, and alkyl peroxides. preferably di-tert-butyl peroxide; anti-oxidant additives, such as aliphatic, aromatic amines, hindered phenols, such as BHT, BHQ; - demulsifiers or demulsifiers; anti-static additives or conductivity improvers; - the dyes; antifoam additives, especially (but not exclusively) chosen, for example, from polysiloxanes, oxyalkylated polysiloxanes, and fatty acid amides derived from vegetable or animal oils; examples of such additives are given in EP861182, EP663000, EP736590; anti-corrosion additives such as ammonium salts of carboxylic acids; chelating agents and / or metal sequestering agents, such as triazoles, disalicylidene alkylene diamines, and especially N, N 'bis (salicylidene) 1,3-propane diamine; cold-holding additives and in particular cloud point-improving additives, in particular (but not limited to) selected from the group consisting of long-chain olefin terpolymers / (meth) acrylic ester / maleimide ester, and ester polymers of fumaric / maleic acids. Examples of such additives are given in EP71513, EP100248, FR2528051, FR2528051, FR2528423, EP112195, EP172758, EP271385, EP291367; anti-sedimentation additives and / or paraffin dispersants in particular (but not exclusively) selected from the group consisting of polyamine-amidated (meth) acrylic acid / alkyl (meth) acrylate copolymers, alkenylsuccinimides derived from polyamines phthalamic acid and double chain fatty amine derivatives; alkylphenol / aldehyde resins; examples of such additives are given in EP261959, EP593331, EP674689, EP327423, EP512889, EP832172; US2005 / 0223631; US5998530; W093 / 14178; polyfunctional cold operability additives chosen in particular from the group consisting of olefin and alkenyl nitrate polymers as described in EP573490; other additives improving the cold resistance and the filterability (CFI), such as the EVA and / or EVP copolymers; acid neutralizers such as cyclic alkyl amines; markers, in particular the markers imposed by the regulation, for example the dyes specific to each type of fuel or fuel. perfuming or masking agents for odors, such as those described in EP1 591514; - Other lubricant additives, anti-wear agents and / or friction modifiers as those described above, including (but not limited to) selected from mono- and polycyclic carboxylic acid derivatives.
[0071] The additive composition according to the present invention can be incorporated into the fuel according to any known method. By way of example, the additive composition may be incorporated in the form of a concentrate comprising said composition and a solvent compatible with the fuel, the composition being dispersed or dissolved in the solvent. Such concentrates generally contain from 20 to 95% by weight of solvents. Solvents are organic solvents which generally contain hydrocarbon solvents. As examples of solvents, mention may be made of petroleum fractions, such as naphtha, kerosene, heating oil; aliphatic and / or aromatic hydrocarbons such as hexane, pentane, decane, pentadecane, toluene, xylene, and / or ethylbenzene and alkoxyalkanols such as 2-butoxyethanol and / or or mixtures thereof. hydrocarbons and optionally co-solvents or compatibilizers, such as 2-ethylhexanol, decanol, isodecanol and / or isotridecanol.
[0072] The additive composition as described above can be used to add fuel. In particular, the additive composition according to the invention is particularly suitable for use in a diesel fuel having a sulfur content of less than or equal to 500 ppm by weight, preferably comprising a biodiesel.
[0073] Diesel fuels are liquid fuels for compression engines. Diesel fuel is understood to mean fuels comprising middle distillates having a boiling point of between 100 and 500 ° C .; their starting crystallization temperature TCC is often greater than or equal to -20 ° C, generally between -15 ° C and + 10 ° C. These distillates are base mixtures which can be chosen, for example, from distillates obtained by the direct distillation of petroleum or crude hydrocarbons, vacuum distillates, hydrotreated distillates, distillates obtained from catalytic cracking and / or hydrocracking. distillates under vacuum, distillates resulting from conversion processes such as ARDS (by atmospheric residue desulfurization) and / or visbreaking. The diesel fuels according to the invention may also contain light cuts such as gasolines from distillation, catalytic or thermal cracking units, isomerization alkylation units, desulfurization units, steam cracking units.
[0074] In addition, the diesel fuels may contain new sources of distillates, among which may be mentioned in particular: the heaviest cuts resulting from cracking and visbreaking processes concentrated in heavy paraffins, comprising more than 18 carbon atoms, synthetic distillates resulting from gas transformation such as those resulting from the Fischer Tropsch process, - synthetic distillates resulting from the treatment of biomass of plant and / or animal origin, such as, in particular, NexBTL, taken alone or as a mixture, - gas oils The diesel fuel according to the invention may also comprise or consist solely of one or more biofuels. By biofuel, we mean fuels obtained from organic matter (biomass), as opposed to fuels from fossil fuels. Examples of known biofuels include biodiesels (also known as biodiesels) and alcohols. Alcohols, such as methanol, ethanol, butanols, ethers, (MTBE, ETBE, etc.) are generally used in admixture with fuel fuels, but sometimes with heavier fuels of the diesel type. Biodiesel or biodiesel is an alternative to conventional diesel fuel. This biofuel is obtained from a vegetable or animal oil (including used cooking oil) transformed by a chemical process called transesterification, reacting this oil with an alcohol to obtain fatty acid esters. With methanol and ethanol, fatty acid methyl esters (EMAG) and fatty acid ethyl esters (EEAG) are obtained respectively. Examples of vegetable and / or animal oils and / or their esters include Methyl or Ethyl Esters of Vegetable Oils or Fatty Acids (EMHV, EEHV, EMAG, EEAG); For vegetable and / or animal oils, mention may be made of hydrotreated vegetable oils and / or animal oils and / or hydrocracked and / or hydrodeoxygenated (HDO).
[0075] Mixtures of middle distillates of fossil origin and biodiesel are generally referred to as the "B" followed by a number indicating the percentage of biodiesel contained in the diesel fuel. Thus, a B99 contains 99% of biodiesel and VA of middle distillates of fossil origin, the B20, 20% of biodiesel and 80% of middle distillates of fossil origin etc ...
[0076] Thus, the BO gas oils which do not contain oxygenated compounds are distinguished from Bx type biodiesel fuels which contain x% (v / v) of vegetable oil esters or of fatty acids, most often methyl esters ( EMHV or EMAG). When biodiesel is used alone in engines, the term fuel is termed B100. In the remainder of this application, we will use the term "diesel fuel" in the broad sense to cover all the fuels described above. The diesel fuel preferably has a sulfur content of less than or equal to 500 ppm by weight, advantageously less than or equal to 100 ppm by mass, and which can reach a content of less than or equal to 50 ppm by mass, or even less than or equal to 10 ppm. mass (this is the case of diesel fuels for current vehicles whose sulfur content according to the European standard EN 590 currently in force must be less than or equal to 10 ppm by mass).
[0077] The diesel fuel preferably comprises up to 30% by volume of biodiesel, preferably up to 20% by volume, more preferably up to 10% by volume. The additive composition is preferably incorporated in the fuel so as to obtain a mass concentration of each additive contained in said composition ranging from 5 to 5000 ppm, preferably from 20 to 500 ppm, more preferably from 30 to 250 ppm. in the fuel. The mass concentration is calculated with respect to the total mass of the fuel.
[0078] In particular, the mass concentration of each first and second additive and optionally the third additive ranges from 5 to 5000 ppm, and preferably from 20 to 500 ppm, more preferably from 30 to 250 ppm. Those skilled in the art will easily adapt the concentration of the additive composition according to the invention as a function of the possible dilution of the additives in a solvent, to obtain the desired concentration of each functional additive in the final fuel. The fuel preferably comprises at least 5 mass ppm, preferably at least 100 ppm by weight of the additive composition according to the invention. Up to 10%, preferably up to 1%, more preferably up to 0.5% by weight of additives including the additive composition may be incorporated in a fuel.
[0079] The mass ratio between the first and second additives (first: second) is between 1: 100 and 100: 1, preferably between 1: 10 and 10: 1, even more preferably between 1: 2 and 2: 1. The mass ratio between the second and third additives (second: third) is between 1: 100 and 1: 1, preferably between 1: 10 and 1: 1, even more preferably between 1: 5 and 1: 1. The diesel fuel described above may be used in a diesel engine, to improve the performance of said engine, in particular to limit deposits in said engine, preferably in a direct injection engine, more preferably when the engine is equipped with a high-pressure injection system ("common-rail"). The use of such an additive fuel with the additive composition according to the present invention makes it possible to reduce the fuel consumption of the diesel engine ("Fuel Eco" action), in particular makes it possible to minimize the power loss of said engine. The present invention also relates to a method for maintaining the cleanliness of the diesel engine ("keep-clean" action) by limiting the deposits of soap and / or varnish in the internal parts of the injection systems of said engine and / or for cleaning the internal parts of the injection system of said engine clogged, at least partly removing the deposits of soap and / or varnish in said internal parts (curative action "clean-up" said method comprises the combustion of an additive composition according to the present invention in a diesel engine, in particular in a direct injection engine, preferably with a high pressure injection system ("commonrail").
[0080] EXAMPLES Reagents - N, N-bis (2-ethylhexyl) -1,2,4-triazole-1-methanamine (CAS 91273-04-0) - Polyisobutenyl-succinic anhydride (PIBSA) with a number average molecular weight Mn of 1100 (GPC) marketed by BASF under the brand name "Glissopal * SA®" - 3-amino-1,2,4-triazole (CAS 61-82-5). Table 1: mass composition of sorbitan partial esters EPS1 and EPS2, determined by steric exclusion chromatography (GPC) Component EPS1 EPS2 (0/0) (0/0) Sorbitol 1,4 0.3 Free fatty acids 1,2 5.9 Sorbitan monooleate 24.7 7.1 Sorbitan dioleate 41.3 30.4 Sorbitan trioleate 28.7 54.3 Unidentified compounds 2.7 1.9 Example 1 - synthesis of additives partial ester of diglycerol : DGMO1 and DMGO2 In the presence of catalyst of the MeONa type, 90 g of diglycerol are reacted at 170 ° C. with 500 g of oleic sunflower oil (oleic acid equivalent concentration under reduced pressure of 300 mbar (0.03 MPa). ) for 6 hours.
[0081] The following procedure is reproduced a second time to prepare a second product sample. Table 2: mass composition of the products obtained DGMO1 and DGMO2 determined by steric exclusion chromatography (GPC) Component DGMO 1 DGMO 2 Monoester diglycerol 24.7 31.4 Diester diglycerol 41.2 30.2 Triester diglycerol 18.6 14 , 4 Diglycerol tetraester 6.6 6.4 Monoglyceride 2.4 nd Diglyceride 1 2.1 Diglycerol nd 3.3 Oleic sunflower methyl ester 5.3 6.4 nd = not determined Example 2: Synthesis of 3-polyisobutene succinimide -1,2,4-triazole In a 500 ml flask, 100 g of polyisobutenyl succinic anhydride (PIBSA) was charged with 84% of active ingredient (76.64 mmol) and 26.3 g of an aromatic solvent of the brand were added. Solvesso 150ND ". After having equipped all of a Dean Starck and placed under a nitrogen atmosphere, the reaction medium is heated to 140 ° C., with vigorous stirring, and then 5.15 g (0.8 eq / 61.31 mmol) of 1,2,4-amino-triazole. Then heated at reflux for 4 hours to remove 1.10 mL of water in the Dean Starck. It is cooled to ambient temperature and then the solvent supplement Solvesso 150ND is added to obtain a product containing 50% of active material. 202.4 g of a clear brown liquid containing 50% active ingredient (50.8% measured) are obtained. The product obtained is a mixture of triazole derivatives in open form (formula II with R1 and R3 = H and R4 = PIB) and in closed form (formula III with R1 and R3 = H and R4 = PIB or R1 and R3 = PIB and R4 = H). The ratio of open to closed form mass percentages determined by GPC analysis is 95: 5.
[0082] Example 3 Synthesis of a Quaternary Ammonium Salt SAQ Preparation of a Nitrogen Compound (a) 500 g (0.38 mol) of polyisobutenyl succinic anhydride (PIBSA) are heated to 70 ° C., charged into a reactor equipped with a Dean Starck and placed under a nitrogen atmosphere. 76.9 g of heptane and 52.3 g (0.51 mol / 1.34 eq.) Of dimethylaminopropylamine (DMAP) are added to the reactor while maintaining the reaction temperature at 70 ° C. during the introduction. The reaction medium is maintained at 70 ° C. for 1 h. The reaction medium is cooled to room temperature. The intermediate product is recovered.
[0083] Quaternization of the Tertiary Amine of the Nitrogen Compound (a) 470 g of the intermediate product is placed in a new 2L reactor equipped with a refrigerant. 180.6 g of 2-ethylhexanol are then introduced and the reaction medium is stirred and heated to 55 ° C. under a nitrogen atmosphere. 40.2 g (0.69 mol) of propylene oxide is then gradually introduced into the medium by means of a syringe pump over a period of 4 hours, while maintaining the reaction temperature at 55 ° C. The mixture is maintained at this temperature for 16 hours. After cooling the medium, the product of the reaction comprising mainly the quaternary ammonium salt derivative SAQ is recovered.
[0084] Samples of said product of the SAQ reaction were analyzed qualitatively by infrared (IR) absorption spectroscopy, mass spectroscopy and NMR. This qualitative analysis made it possible to determine the main components present in the product of the reaction by comparison with reference spectra and taking into account the dilution rates.
[0085] Quantitative analysis on dry residue was also carried out by 13C NMR and by use of an internal standard. The mass composition of the SAQ product measured using the techniques described above is indicated in Table 3 below. Table 3 Components% by weight Quaternary ammonium salt - succinamide form 69.5 Quaternary ammonium salt - succinimide form 6.8 PIBSA 1.7 residual reagents (DMAP-propylene oxide ..) 8.4 PIB 10.2 Other Functionalized PIBs 3.4 TEST PROTOCOLS Protocol 1: Evaluation of Lacquering Resistance for IDID-type Deposits In order to test the performance of these additives according to the invention, the inventors have also developed a new and reliable method. robust to assess the sensitivity of diesel fuels, especially those of superior quality, to lacquering. This method, unlike the methods described in the publications cited above, is not a laboratory method but is based on motor tests and is therefore of technical interest and makes it possible to quantify the effectiveness of the additives or compositions of additives against lacquering. Lacquering measurement method developed by the inventors is detailed below: - The engine used is a Renault K9K702 engine, four cylinders and 16-valve diesel common rail high-pressure injection of a cylinder capacity of 1,500 cm3 and a power of 65kW: the fuel injection pressure regulation is done in the high pressure part of the pump. - The power point at 4,000 rpm is used for a period of 40 hours; the position of the injector in the chamber is lowered by 1 mm from its nominal position, which on the one hand promotes the release of thermal energy from combustion, and on the other hand brings the injector closer to the chamber of combustion. - The injected fuel flow rate is adjusted to obtain an exhaust temperature of 750 ° C at the start of the test. - The injection advance has been increased by 1.5 ° crankshaft compared to the nominal setting (we go from + 12.5 ° to + 14 ° crankshaft) always in order to increase the thermal stresses experienced by the nozzle of the injector. - Finally, to increase the stresses on the fuel, the injection pressure has been increased by 10 MPa compared to the nominal pressure (that is to say from 140 MPa to 150 MPa) and the temperature is regulated. at 65 ° C at the high pressure pump inlet. The technology used for the injectors requires a high fuel return, which promotes fuel degradation since it can be subjected to several cycles in the pump and the high pressure chamber before being injected into the combustion chamber. A variant of the method for testing the clean-up effect (i-e cleaning of deposits of type 1 and / or type 2) has also been developed. It is based on the previous method but is divided into two parts of 40h and 30h: - The first 40 hours are performed with a B7 diesel of high quality containing 330 ppm mass of a PIBSI type detergent and 200 ppm mass of a predominantly oleic acid fatty acid mixture with an acid number of 180 mg KOH / g, this mixture being known for its tendency to generate lacquering deposits. After 40h, two of the four injectors are disassembled and sides to validate the quantity of deposits that are present and two new injectors are then installed instead. - The last 30 hours of the test are performed with the product to be evaluated. At the end of the test (70h total), the injectors are disassembled and sides. At the end of the test, three batches of two injectors are available: - Lot 1: 2 injectors having seen 40 hours of high quality fuel known for its tendency to generate "lacquering" described above. - Lot 2: 2 injectors having seen 40h of high quality fuel known for its tendency to generate "lacquering" described above + 30h of product to be evaluated. - Lot 3: 2 injectors having seen 30h product to evaluate.
[0086] Expression of results To ensure the validity of the result, various parameters are checked during the test: power, torque and fuel consumption indicate whether the injector clogs up or if its operation is deteriorated by a formation of deposits since the operating point is the same throughout the test. The characteristic temperatures of the various fluids (coolant, fuel, oil) make it possible to check the validity of the tests. The fuel is regulated at 65 ° C at the pump inlet, the coolant is regulated at 90 ° C at the motor output.
[0087] The flue gas values make it possible to control the ignition timing at the beginning of the test (target value of 3FSN) and to ensure that it is repeatable from one test to another.
[0088] The injectors are disassembled at the end of the test to visualize and dimension the deposits formed along the needles. The procedure for the quotation of the selected hands is as follows: The surface of the needle is divided into 100 points. For each point, a quotation of the deposit of soap (type 1) and varnish (type 2) is carried out. The zone of the cylinder (directly following the conical part) represents 68% of the overall quotation of the needle and the zone of the cone represents 32% of the overall quotation of the needle; To facilitate the quotation, each of these two zones is divided into 4. In Figure 4, the indicated% correspond to a quarter of the surface of the needles: the overall surface weighting is therefore 17x4 = 68%.
[0089] For soaps (deposits type 1), the scale of the quotations varies from -1 (case of a very fine soap) to -10 (case of a very thick soap strongly colored). A value of the impact of soap is determined by calculating the arithmetic mean of the quotations obtained on the population of points of the quoted needle.30 For varnishes (type 2 deposits), the scale of the notes varies from 1 (case of a black varnish equivalent to a large deposit of varnish) to 10 (case of a very clear varnish equivalent to a new needle). A value of the impact of the varnish is calculated by summing the number of points belonging to the quotation (1 to 10) divided by the value of the quotation. An overall score (N) of 10 is then determined by weighting the impact of varnishes and soaps. Thus, for the properties of maintenance of engine cleanliness ("keepclean" action), a product performance threshold was determined with respect to this rating procedure: N <7.5 = Not satisfactory, N 7.5 = Satisfactory . For the cleaning properties of the internal parts of the fouled engine injection system ("clean-up" curative action), a product performance threshold was determined with respect to this quotation procedure: Mien 2- Nlot 1) <1 , 55 = Unsatisfactory, 4 (NI ° t-NGlot 1) 1.55 = Satisfactory.
[0090] Protocol 2: Measurement of power loss in a diesel engine with high pressure injection system (DW10 + Zn) The fuel is tested in a Peugeot DW10 engine using injectors meeting the Euro 5 standards according to the CEC method F-98-8 DW1OBTED4 developed and published by The Coordinating European Council (CEC). In order to reproduce the actual conditions of a modern diesel engine, a small amount of zinc neodecanoate (1 ppm) is added to the test fuel. This test was developed to discriminate fuels on the basis of their ability to produce or avoid external deposits of the injection system relating to coking (in English "coking") or clogging of injection nozzles (English "nozzle"). coking "or" fouling "). This test makes it possible to differentiate the fuels on the basis of the power loss induced by the coking-type deposits (comparison between the% of power loss). This test makes it possible to differentiate a fuel that produces little coking-type deposit (loss of power <2%) and those that produce enough to induce a loss of power of 2% or more, considered unacceptable for engine manufacturers. .
[0091] The test according to the CEC F-98-8 DW 10 protocol is summarized below: Euro 4 Peugeot DW1OBTED4 2.0L, HDi engine, turbodiesel, 4-cylinder in-line with variable geometry turbocharger and exhaust gas recirculation system ( RGE) Displacement: 1998 cm3 Combustion chamber: 4 valves, direct injection Power: 100 Kw at a speed of 4000 rpm Torque: 320 Nm at a speed of 2000 rpm Injection system: Common rail with injectors 6 holes controlled per piezoelectric system (EURO IV) Max. : 1600bars Emissions control: Complies with Euro 4 limit values taking into account exhaust aftertreatment system. The test is divided into the following stages: 0- Injector run-in stage: 16 cycles of 1 hour using a non-fouling reference fuel consisting of a gas oil representative of the French market (B7 = diesel fuel manufactured in France containing 7% FAME) (methyl ester of fatty acids) and responding to EN 590) The test of the fuel to be evaluated then lasts 44 hours in total, not counting the periods of preparation and cooling. The 44 hours are divided into 32 hours of engine operation and 12 hours of engine shutdown. 1- Engine heating step: 30 1 cycle of 12 minutes according to the following speed: Step Tps Speed (rpm) Torque (Nm) (min) 1 2 Stop <5 2 3 2000 50 3 4 3500 75 4 3 4000 100 The motor is then raised to a maximum load of 4000 rpm for 7 minutes and the average power is measured over 30s. 2- Stage of operation: 8 cycles of 1 hour following: Stage Tps Regime Charge Torque Temperature (min) (rpm) (%) (Nm) of air after exchanger (° C) 1 2 1750 20 62 45 2 7 3000 60 173 50 3 2 1750 20 62 45 4 7 3000 80 212 50 5 2 1750 20 62 45 6 10 4000 100 50 7 2 1250 (10) 20 43 8 7 3000 100 50 9 2 1250 (10) 20 43 10 2000 100 50 11 2 1250 (10) 20 43 12 7 4000 100 50 10 At the end of the cycle, the engine speed is reduced to 1000 rpm / 10Nm in 60s and maintained at this speed for 300s. 3- Cooling stage: 60 seconds of cooling at standstill followed by 10 seconds at standstill. 4- Maceration step: 4 hours engine stop.
[0092] The global cycle 1 to 4 is repeated 4 times. The power loss is measured at each operating cycle, ie 32 in total. TEST Test 1 according to protocol 1: resistance to "lacquering" According to the procedure for evaluating the properties of maintenance of engine cleanliness (preventive action "keep-clean") and cleaning the internal parts of the engine injection system fouled (curative action "clean-up"), described above (Protocol 1), it evaluates the performance of several additive compositions introduced into a diesel matrix representative of the French market (B7 = diesel manufactured in France containing 7% d EMAG (methyl ester of fatty acids) and answering EN 590). The details for each fuel tested, as well as the results obtained, are indicated in Table 4. Attention, the tests G, G 'and G "correspond to the same test, G corresponding to the result for the batch of injectors 1, G' corresponding to the result for the batch of injectors 2 and G "corresponding to the result for the batch of injectors 3. The test G corresponds to the phase of fouling (" Dirty-up "), the test G 'to the phase The "clean-up" and the G "clean-up" tests are the "keep-clean" quantities and the quantities given in Table 4 are mass quantities (mg / kg). Fuel number 1 2 3 4 5 GIG 'IG' GIG 'G' GIG 'IG' GIG IG 'GIG' G 'Diesel fuel matrix B7 B7 B7 B7 B7 B7 3-polyisobutene succinimide- - - 200 200 - - - - - - - 50 50 - - - 1,2,4-triazole (ppm) EPS1 (ppm) - - - - - 200 200 - - - - - - 200 200 EPS2 (ppm) _ - - - - - - - - - - 200 200 - - - SAQ (ppm) _ - - - - - - 50 50 - 50 50 - 50 50 N, N-bis (2-ethylhexyl) ) -1,2,4- - _ _ _ _ _ _ _ _ _ _ - - 5 triazole-1-methanamine (ppm) Overall Note (N) 9,6 5,6 5,52 9,55 6, 90 6.99 9.43 4.92 5.19 9.91 6.54 8.32 9.04 5.6 6.48 9.52 A (Ne. N o) -0, 08 -0, 09 0.27 1.78 0, 88 "keep-clean" effect (yes / no) * yes yes yes yes yes "clean-up" effect (yes / no) * no no no yes no *: irrelevant These tests demonstrate the curative effectiveness (clean up action) of the additive compositions according to the present invention, that is to say their ability to eliminate deposits of varnish types or soaps already formed on the needles since the quotation of the set of injectors G 'is greater than that of the injector batch G (there has been a beginning of significant cleaning of the needle), and also confirms their preventive effectiveness (keep-clean action) since the rating of the set of injectors G "is markedly high.We do not observe a curative effect (action clean up) when using fuels 1, 2 or 3. Thus, we deduce that the first, second and third additives used alone in the fuel B7 do not provide curative effect to said fuel, relative to soap-like deposits and / or varnish. Note that fuel 4 containing a combination of the first, second and third additives has both preventive (Keep-clean) and curative (Clean-up) effect. In addition, it is found that comparatively, the fuel containing a triazole derivative not covered by the present invention has no significant curative effect (Clean-up).
[0093] Test 2 according to protocol 2: resistance to coking, the power loss of several additive compositions introduced into the diesel matrix representative of the French market (B7 = diesel fuel manufactured in France containing 7% of EMAG (methyl ester of fatty acids) and responding to EN 590) according to protocol 2 (DW10 + Zn) described above. The details of each fuel tested, as well as the results obtained, are given in Table 5. The quantities indicated in Table 5 are mass quantities (mg / kg). Table 5 Fuel number [6 [7 [8 9 10 11 Diesel fuel matrix B7 B7 B7 B7 B7 B7 3-polyisobutene succinimide-1,2,4- 50 50 50 triazole (ppm) EPS2 (ppm) 200 SAQ (ppm) 50 50 50 50 50 N, N-bis (2-ethylhexyl) ) -1,2,4-triazole-1-methanamine (ppm) 5 8 Loss of potency (%) -0.1 -6.7 -5.05 -5.51 0.1 0.12 Fuels containing the additive composition according to the present invention are particularly remarkable in that they do not generate a coking deposit as compared to a fuel containing a quaternary ammonium salt alone (fuel 7) or a combination of a salt of quaternary ammonium with a triazole derivative different from those covered by the present invention (fuels 8 and 9).
[0094] The specific choice of a triazole derivative according to the invention in combination with a quaternary ammonium salt and optionally a compound A as described above (fuels 10 and 11) confers on the fuel both the control of the lacquering type (IDID deposit) and a coking type deposit resistance.
[0095] The additive composition according to the present invention is remarkable in that it makes it possible to obtain fuels with improved performance, in particular for low-sulfur fuels with gasolines possibly containing a biodiesel. The particular additive combination described above makes it possible in particular to reduce the fuel consumption of diesel engines, by combining a clean-up and keep-clean effect, by minimizing the power loss and improving the wear resistance of said engine. fuel.

权利要求:
Claims (33)
[0001]
REVENDICATIONS1. A fuel additive composition comprising at least: - a first additive comprising a triazole derivative of the following formula (I): R2 R3 R1 wherein: R 1 is chosen from the group consisting of a hydrogen atom, a linear or branched C 1 -C 8 aliphatic hydrocarbon group and a carboxyl group (-CO 2 H), R2 and R5 are identical or different and represent, independently of each other, a group chosen from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated C1-C33 aliphatic hydrocarbon group, optionally comprising one or more oxygen atoms in the form of carbonyl (-CO-) and / or carboxyl (-CO2H) functions, said R2 and R5 groups optionally together forming a ring of 5 to 8 atoms including the nitrogen to which R2 is bound, it being understood that in this case R2 and R5 then constitute one and the same linear or branched, saturated or unsaturated, C1 to C33 aliphatic hydrocarbon group, optionally substituted with one or more oxygen atoms in the form of a carbonyl function (-CO-) and / or carboxyl (- CO2H),. R3 and R4 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated, cyclic or acyclic aliphatic hydrocarbon group having from 2 to 200 carbon atoms, - a second additive comprising a quaternary ammonium salt obtained by reaction of a nitrogen compound comprising a tertiary amine function with a quaternization agent, said nitrogenous compound being chosen from: a) the product of the reaction of a hydrocarbon-substituted acylating agent and a compound comprising at least one tertiary amine group and a group selected from primary amines, secondary amines and alcohols; b) a product of the Mannich reaction; comprising a tertiary amine group; and c) amines substituted with a polyalkene group having at least one tertiary amine group.
[0002]
2. Composition according to claim 1, characterized in that the triazole derivative has the formula (I) in which R3 and R4 are identical or different and represent, independently of one another, a group chosen from the group consisting of a hydrogen atom and an aliphatic hydrocarbon group having a number average molecular weight (Mn) of between 200 and 3000.
[0003]
3. Composition according to one of claims 1 and 2, characterized in that the triazole derivative is represented by the following formula (II): (II) wherein R1, R3 and R4 are as defined in one of the claims 1 and 2.
[0004]
4. Composition according to one of claims 1 and 2, characterized in that the triazole derivative is represented by the following formula (III): (III) wherein R1, R3 and R4 are as defined in one of the claims 1 and 2.
[0005]
5. Composition according to one of claims 1 and 2, characterized in that the first additive comprises a mixture of triazole derivatives of formulas (II) and (III) as defined respectively in claims 3 and 4.
[0006]
6. Composition according to any one of claims 1 to 5, characterized in that the triazole derivative is obtained by reaction of an aminotriazole of formula (IV) with a diacid of formula (V) and / or a succinic anhydride of following (VI): (v) (VI) wherein R1, R3 and R4 are as defined in one of claims 1 and 2.
[0007]
7. Composition according to any one of claims 1 to 6, characterized in that the quaternarisation agent is selected from the group consisting of dialkyl sulfates, carboxylic acid esters, alkyl halides, halides of benzyl, hydrocarbon carbonates and hydrocarbon epoxides optionally in admixture with an acid, alone or in admixture.
[0008]
8. Composition according to any one of claims 1 to 7, characterized in that the nitrogen compound comprises a reaction product of a acylation agent substituted with a hydrocarbon group and an amine of formula (VII) or (VIII) R6 R6 R8 N-X -Nd N -X - [O (CH2) AnOH R7 R7 (V11) (VIII) wherein R6 and R7 are the same or different and represent, independently of one another, an alkyl group having 1 to 22 carbon atoms; X is an alkylene group having 1 to 20 carbon atoms; m is an integer from 1 to 5; n is an integer from 0 to 20; and R8 is a hydrogen atom or an alkyl group having 1 to 22 carbon atoms.
[0009]
9. Composition according to any one of claims 1 to 8, characterized in that it further comprises a third additive comprising at least 50% by weight of a compound A selected from partial esters of polyols and aliphatic hydrocarbons saturated or unsaturated, linear or branched, cyclic or acyclic C -C monocarboxylic, said partial esters may be taken alone or in admixture.
[0010]
10. Composition according to claim 9, characterized in that said compound A comprises x ester unit (s), y hydroxyl unit (s) and z unit (s) ether, x, y and z being integers such that x varies from 1 to 10, y varies from 1 to 10, and z ranges from 0 to 6.
[0011]
11. Composition according to one of claims 9 and 10, characterized in that the distribution in ester units, hydroxyl and ether in said compound A is such that x varies from 1 to 4, y varies from 1 to 7 and z varies from 1 to 3.
[0012]
12.Composition according to any one of claims 9 to 11, characterized in that the compound A is obtained by esterification between: - one or more C4 to C36 fatty acid (s) optionally comprising one or more ethylenic bonds; and a linear or branched, cyclic or acyclic polyol optionally comprising a heterocycle of 5 to 6 atoms, preferably a heterocycle of 4 to 5 carbon atoms and an oxygen atom, substituted by hydroxyl groups.
[0013]
13. Composition according to claim 12, characterized in that the fatty acids are chosen from the group consisting of stearic acid, isostearic acid, linolenic acid, oleic acid, linoleic acid, behenic acid, arachidonic acid, ricinoleic acid, palmitic acid, myristic acid, lauric acid and capric acid, taken alone. or in mixture.
[0014]
14. Composition according to one of claims 12 and 13, characterized in that the polyol is chosen from polyols comprising more than three hydroxyl functions and polyols comprising at least one heterocycle of 5 or 6 atoms, preferably heterocycles of 4 to 5 carbon atoms and one oxygen atom, optionally substituted with hydroxyl groups.
[0015]
15. Composition according to any one of claims 12 to 14, characterized in that the polyol is chosen from polyols comprising at least two heterocycles of 4 or 5 carbon atoms and an oxygen atom, connected by the formation. an acetal bond between a hydroxyl function of each ring, said heterocycles being optionally substituted with hydroxyl groups.
[0016]
16.Composition according to any one of claims 9 to 15, characterized in that the polyol is selected from the group consisting of erythritol, xylitol, arabitol, ribitol, sorbitol, malitol, isomalitol , lactitol, volemitol, mannitol, pentaerythritol, 2-hydroxymethyl-1,3-propandediol, 1,1,1-tri (hydroxymethyl) ethane, trimethylolpropane, sorbitan and carbohydrates such as sucrose, fructose, maltose, glucose and sucrose.
[0017]
17. Composition according to any one of claims 9 to 16, characterized in that compound A is chosen from partial esters of sorbitan, preferably sorbitan mono-, di- and tri-esters, taken alone or as a mixture more preferably the partial esters of sorbitan comprising more than 40% by mass of sorbitan triesters.
[0018]
18.Composition according to any one of claims 9 to 14, characterized in that the compound A is chosen from monoester (s) and / or diester (s) of polyglycerols having from 2 to 5 glycerol units per molecule.
[0019]
19. Composition according to Claim 18, characterized in that the compound A is chosen from monoester (s) and / or diester (s) of polyglycerols derived from fatty acid (s), having more than 50% by number of the chains. greases comprising between 12 and 24 carbon atoms.
[0020]
20. Composition according to one of claims 18 and 19, characterized in that the compound A is chosen from monoester (s) and / or diester (s) of diglycerol and / or triglycerol.
[0021]
21. Composition according to claim 20, characterized in that the partial esters of diglycerol and / or triglycerol comprise at least 50% by weight of monoester (s) and / or diester (s) of oleic acid and diglycerol.
[0022]
22. Use of an additive composition as defined in any one of claims 1 to 2, in a diesel fuel having a sulfur content of less than or equal to 500 ppm by weight, preferably comprising a biodiesel.
[0023]
23. A diesel fuel having a sulfur content of less than or equal to 500 ppm by weight comprising at least 5 ppm by weight of an additive composition as defined in any one of Claims 1 to 21. 10
[0024]
24. Diesel fuel according to claim 23, characterized in that it comprises up to 30% volume of biodiesel.
[0025]
25. Fuel according to one of claims 23 and 24, characterized in that it comprises in addition at least one or more other additives selected from antioxidants, combustion improvers, corrosion inhibitors, additives of cold-held, dyes, demulsifiers, metal deactivators, defoamers, cetane improvers, lubricant additives, co-solvents and compatibilizers. 20
[0026]
26. Fuel according to any one of claims 23 to 25, characterized in that the mass concentration of each first and second additive and optionally third additive ranges from 5 to 5000 ppm.
[0027]
27. Use of a diesel fuel as defined in any one of claims 23 to 26 in a diesel engine for improving the performance of said engine.
[0028]
28. Use according to claim 27, for limiting deposits in said diesel engine. 30
[0029]
29. Use according to one of claims 27 and 28, characterized in that the engine is a direct injection engine, preferably a high-pressure injection system ("common-rail").
[0030]
30. Use according to any one of claims 27 to 29, to reduce the fuel consumption of said engine ("Fuel Eco" action).
[0031]
31. Use according to any one of claims 27 to 30, to minimize the power loss of said engine.
[0032]
32. Use according to any one of claims 27 to 31, for maintaining the cleanliness of said motor ("keep-clean" action) by limiting the deposits of soap and / or varnish in the internal parts of the injection systems of said engine.
[0033]
33. Use according to any one of claims 27 to 32, for cleaning the fouled internal parts of the injection system of said engine, at least partly removing the deposits of soap and / or varnish in said internal parts (curative action "Clean-up"). 15

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同族专利:

---

公开号 | 公开日

---

CN106029844B|2018-08-10|

---

US20170058225A1|2017-03-02|

---

EA201691729A1|2016-12-30|

---

FR3017876B1|2016-03-11|

---

JP6456406B2|2019-01-23|

---

CN106029844A|2016-10-12|

---

CA2939363A1|2015-08-27|

---

WO2015124584A1|2015-08-27|

---

US10280380B2|2019-05-07|

---

JP2017506288A|2017-03-02|

---

TW201540706A|2015-11-01|

---

EP3110928A1|2017-01-04|

---

AR099522A1|2016-07-27|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

US4257779A|1976-12-23|1981-03-24|Texaco Inc.|Hydrocarbylsuccinic anhydride and aminotriazole reaction product additive for fuel and mineral oils|

---

US4282007A|1980-09-22|1981-08-04|Texaco Inc.|Novel fuel composition containing alcohol|

---

US4604102A|1985-11-25|1986-08-05|Ethyl Corporation|Fuel compositions|

---

US20120010112A1|2010-07-06|2012-01-12|Basf Se|Acid-free quaternized nitrogen compounds and use thereof as additives in fuels and lubricants|

---

US20120210966A1|2011-02-22|2012-08-23|Afton Chemical Corporation|Fuel additives to maintain optimum injector performance|

---

WO2013120985A1|2012-02-17|2013-08-22|Total Raffinage Marketing|Additives for improving the resistance to wear and to lacquering of diesel or biodiesel fuels|

---

DE1248643B|1959-03-30|1967-08-31|The Lubrizol Corporation, Cleveland, Ohio |Process for the preparation of oil-soluble aylated amines|

---

NL124842C|1959-08-24|

---

NL124306C|1959-08-24|

---

US3231587A|1960-06-07|1966-01-25|Lubrizol Corp|Process for the preparation of substituted succinic acid compounds|

---

US3778371A|1972-05-19|1973-12-11|Ethyl Corp|Lubricant and fuel compositions|

---

US4171959A|1977-12-14|1979-10-23|Texaco Inc.|Fuel composition containing quaternary ammonium salts of succinimides|

---

US4253980A|1979-06-28|1981-03-03|Texaco Inc.|Quaternary ammonium salt of ester-lactone and hydrocarbon oil containing same|

---

US4326973A|1981-01-13|1982-04-27|Texaco Inc.|Quaternary ammonium succinimide salt composition and lubricating oil containing same|

---

US4338206A|1981-03-23|1982-07-06|Texaco Inc.|Quaternary ammonium succinimide salt composition and lubricating oil containing same|

---

FR2510598B1|1981-07-30|1985-01-18|Inst Francais Du Petrole|

---

FR2528066B1|1982-06-04|1985-02-22|Inst Francais Du Petrole|

---

FR2528051B1|1982-06-08|1986-05-02|Inst Francais Du Petrole|NITROGEN ADDITIVES FOR USE AS DISORDERS TO REDUCE THE POINT OF MEDIUM HYDROCARBON DISTILLATES AND COMPOSITIONS OF MEDIUM HYDROCARBON DISTILLATES CONTAINING THE ADDITIVES|

---

FR2528423B1|1982-06-10|1987-07-24|Inst Francais Du Petrole|NITROGEN ADDITIVES FOR USE AS DISORDERS TO REDUCE THE POINT OF MEDIUM HYDROCARBON DISTILLATES AND COMPOSITIONS OF MEDIUM HYDROCARBON DISTILLATES CONTAINING THE ADDITIVES|

---

FR2535723B1|1982-11-09|1985-01-18|Inst Francais Du Petrole|

---

FR2567536B1|1984-07-10|1986-12-26|Inst Francais Du Petrole|ADDITIVE COMPOSITIONS, IN PARTICULAR FOR IMPROVING THE COLD FILTRABILITY PROPERTIES OF MEDIUM OIL DISTILLATES|

---

EP0261959B1|1986-09-24|1995-07-12|Exxon Chemical Patents Inc.|Improved fuel additives|

---

FR2607139B1|1986-11-21|1989-08-18|Inst Francais Du Petrole|POLYMERS WITH NITROGEN FUNCTIONS DERIVED FROM UNSATURATED POLYESTERS AND THEIR USE AS ADDITIVES FOR LOWERING THE FLOW POINT OF MEDIUM HYDROCARBON DISTILLATES|

---

FR2613371B1|1987-04-01|1989-07-07|Inst Francais Du Petrole|NITROGENATED COPOLYMERS, THEIR PREPARATION AND THEIR USE AS ADDITIVES FOR IMPROVING THE FLOW PROPERTIES OF MEDIUM HYDROCARBON DISTILLATES|

---

FR2626578B1|1988-02-03|1992-02-21|Inst Francais Du Petrole|AMINO-SUBSTITUTED POLYMERS AND THEIR USE AS ADDITIVES FOR MODIFYING THE COLD PROPERTIES OF MEDIUM HYDROCARBON DISTILLATES|

---

GB9104138D0|1991-02-27|1991-04-17|Exxon Chemical Patents Inc|Polymeric additives|

---

FR2676062B1|1991-05-02|1993-08-20|Inst Francais Du Petrole|AMINO-SUBSTITUTED POLYMER AND THEIR USE AS ADDITIVES FOR MODIFYING THE COLD PROPERTIES OF MEDIUM HYDROCARBON DISTILLATES.|

---

US5254138A|1991-05-03|1993-10-19|Uop|Fuel composition containing a quaternary ammonium salt|

---

GB9200694D0|1992-01-14|1992-03-11|Exxon Chemical Patents Inc|Additives and fuel compositions|

---

GB9208034D0|1992-04-10|1992-05-27|Bp Chem Int Ltd|Fuel composition|

---

GB9219962D0|1992-09-22|1992-11-04|Exxon Chemical Patents Inc|Additives for organic liquids|

---

ES2103066T3|1992-10-09|1997-08-16|Inst Francais Du Petrole|AMINE PHOSPHATES INCLUDING A TERMINAL IMIDA CYCLE, ITS PREPARATION AND ITS USE AS ADDITIVES FOR MOTOR FUELS.|

---

FR2699550B1|1992-12-17|1995-01-27|Inst Francais Du Petrole|Composition of petroleum middle distillate containing nitrogenous additives usable as agents limiting the rate of sedimentation of paraffins.|

---

GB9301119D0|1993-01-21|1993-03-10|Exxon Chemical Patents Inc|Fuel composition|

---

FR2735494B1|1995-06-13|1997-10-10|Elf Antar France|BIFUNCTIONAL COLD-RESISTANT ADDITIVE AND FUEL COMPOSITION|

---

GB9514480D0|1995-07-14|1995-09-13|Exxon Chemical Patents Inc|Additives and fuel oil compositions|

---

FR2751662B1|1996-07-29|1998-10-23|Total Raffinage Distribution|MIXED ORGANOMETALLIC COMPOSITION COMPRISING AT LEAST THREE METALS AND THEIR APPLICATIONS AS ADDITIVES FOR FUELS OR FUELS|

---

FR2751982B1|1996-07-31|2000-03-03|Elf Antar France|ONCTUOSITY ADDITIVE FOR ENGINE FUEL AND FUEL COMPOSITION|

---

WO1998011178A1|1996-09-13|1998-03-19|Exxon Research And Engineering Company|Polyol ester distillate fuels additive|

---

DE59708189D1|1997-01-07|2002-10-17|Clariant Gmbh|Improving the flowability of mineral oils and mineral oil distillates using alkylphenol-aldehyde resins|

---

US6784317B2|2001-05-02|2004-08-31|Mitsubishi Gas Chemical Company, Inc|Production of quaternary ammonium salt of hydroxycarboxylic acid and quarternary ammonium salt of inorganic acid|

---

DE10211418A1|2002-03-15|2003-09-25|Bayer Ag|Process for the production of highly reactive polyisobutenes|

---

US20050223631A1|2004-04-07|2005-10-13|Graham Jackson|Fuel oil compositions|

---

FR2869621B1|2004-04-30|2008-10-17|Total France Sa|USE OF ADDITIVES FOR IMPROVING ODOR OF HYDROCARBON COMPOSITIONS AND HYDROCARBON COMPOSITIONS COMPRISING SUCH ADDITIVES|

---

KR101314378B1|2005-06-16|2013-10-15|더루우브리졸코오포레이션|Quaternary ammonium salt detergents for use in fuels|

---

FR2888248B1|2005-07-05|2010-02-12|Total France|LUBRICATING COMPOSITION FOR HYDROCARBON MIXTURE AND PRODUCTS OBTAINED|

---

GB0515998D0|2005-08-03|2005-09-07|Ass Octel|Fuel additives|

---

US7906470B2|2006-09-01|2011-03-15|The Lubrizol Corporation|Quaternary ammonium salt of a Mannich compound|

---

DK1914295T5|2006-10-11|2014-03-17|Total Marketing Services|Lubricant for ship engines that use fuel oil with low or high sulfur content|

---

US20080113890A1|2006-11-09|2008-05-15|The Lubrizol Corporation|Quaternary Ammonium Salt of a Polyalkene-Substituted Amine Compound|

---

FR2912932B1|2007-02-23|2011-06-10|Total France|AQUEOUS SOLUTION FOR THE TREATMENT OF EXHAUST GASES FROM DIESEL ENGINES|

---

FR2919293B1|2007-07-27|2009-11-06|Total France Sa|GRAFTING-MODIFIED ETHYLENE AND VINYL ESTERS, PROCESS FOR PREPARING THEM AND THEIR APPLICATION AS ADDITIVES IMPROVING THE COLD PROPERTIES OF LIQUID HYDROCARBONS|

---

FR2925909B1|2007-12-26|2010-09-17|Total France|BIFUNCTIONAL ADDITIVES FOR LIQUID HYDROCARBONS OBTAINED BY GRAFTING FROM COPOLYMERS OF ETHYLENE AND / OR PROPYLENE AND VINYL ESTERS|

---

FR2928934B1|2008-03-20|2011-08-05|Total France|MARINE LUBRICANT|

---

FR2932813B1|2008-06-18|2010-09-03|Total France|LUBRICANT CYLINDER FOR MARINE ENGINE TWO TIMES|

---

EP2430131B1|2009-05-15|2017-09-06|The Lubrizol Corporation|Quaternary ammonium amide salts|

---

FR2953344B1|2009-11-27|2012-01-20|Snecma|METHOD AND APPARATUS FOR REAL-TIME CONTROL OF A FUEL FLOW MEASUREMENT SYSTEM|

---

DK2512662T3|2009-12-16|2014-08-11|IFP Energies Nouvelles|Catalyst for use in hydrotreating comprising metals of groups VIII and VIB and preparation with acetic acid and dialkyl succinate C1-C4|

---

GB201003973D0|2010-03-10|2010-04-21|Innospec Ltd|Fuel compositions|

---

HUE052753T2|2010-07-06|2021-05-28|Basf Se|Composés azotés quaternisés exempts d'acide et leur utilisation comme additifs pour carburants et lubrifiants|

---

FR2969620B1|2010-12-23|2013-01-11|Total Raffinage Marketing|MODIFIED ALKYLPHENOL ALDEHYDE RESINS, THEIR USE AS ADDITIVES IMPROVING THE COLD PROPERTIES OF LIQUID HYDROCARBON FUELS AND FUELS|

---

FR2972648B1|2011-03-18|2013-04-26|Ifp Energies Now|CATALYST FOR USE IN HYDROTREATMENT COMPRISING METALS OF GROUP VIII AND VIB AND PREPARATION WITH CITRIC ACID AND C1-C4 DIALKYL SUCCINATE|

---

FR2974111B1|2011-04-14|2013-05-10|Total Raffinage Marketing|LUBRICANT CYLINDER FOR MARINE ENGINE TWO TIMES|

---

FR2991992B1|2012-06-19|2015-07-03|Total Raffinage Marketing|ADDITIVE COMPOSITIONS AND THEIR USE TO ENHANCE THE COLD PROPERTIES OF FUELS AND FUELS|

---

FR3002235B1|2013-02-19|2015-02-27|Total Raffinage Marketing|LUBRICANT COMPOSITION BASED ON AMINO COMPOUNDS|

---

FR3005061B1|2013-04-25|2016-05-06|Total Raffinage Marketing|ADDITIVE FOR IMPROVING THE STABILITY OF OXIDATION AND / OR STORAGE OF LIQUID HYDROCARBON FUELS OR FUELS|

---

FR3005474B1|2013-05-07|2016-09-09|Total Raffinage Marketing|LUBRICANT FOR MARINE ENGINE|DE68923506T2|1988-09-13|1996-03-28|Asahi Optical Co Ltd|Single-lens reflex camera system.|

---

US5093680A|1988-09-22|1992-03-03|Asahi Kogaku Kogyo Kabushiki Kaisha|Image magnification control device for a camera|

---

FR3045657B1|2015-12-22|2020-09-11|Total Marketing Services|DETERGENT ADDITIVE FOR FUEL AND COPOLYMERS FOR USE IN THIS APPLICATION|

---

FR3071850B1|2017-10-02|2020-06-12|Total Marketing Services|COMPOSITION OF FUEL ADDITIVES|

---

PL3710565T3|2017-11-17|2021-11-29|Dorf Ketal Chemicals Fze|Fuel additive compositions, and method of use thereof|

---

KR101950489B1|2018-07-11|2019-02-20|주식회사 동이기술|Additive composition for Automobile fuels|

---

FR3087788B1|2018-10-24|2021-06-25|Total Marketing Services|FUEL ADDITIVES ASSOCIATION|

---

FR3103812A1|2019-11-29|2021-06-04|Total Marketing Services|Use of alkyl phenol compounds as detergency additives|

---

FR3103815B1|2019-11-29|2021-12-17|Total Marketing Services|Use of diols as detergency additives|

---

FR3110913A1|2020-05-29|2021-12-03|Total Marketing Services|Engine fuel additive composition|

法律状态:
2015-02-20| PLFP| Fee payment|Year of fee payment: 2 |

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2016-01-21| PLFP| Fee payment|Year of fee payment: 3 |

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2017-01-24| PLFP| Fee payment|Year of fee payment: 4 |

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2018-01-23| PLFP| Fee payment|Year of fee payment: 5 |

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2020-01-22| PLFP| Fee payment|Year of fee payment: 7 |

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2021-02-24| PLFP| Fee payment|Year of fee payment: 8 |

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2022-02-16| PLFP| Fee payment|Year of fee payment: 9 |

优先权:

---

申请号 | 申请日 | 专利标题

---

FR1451437A|FR3017876B1|2014-02-24|2014-02-24|COMPOSITION OF ADDITIVES AND PERFORMANCE FUEL COMPRISING SUCH A COMPOSITION|FR1451437A| FR3017876B1|2014-02-24|2014-02-24|COMPOSITION OF ADDITIVES AND PERFORMANCE FUEL COMPRISING SUCH A COMPOSITION|

---

US15/119,807| US10280380B2|2014-02-24|2015-02-17|Composition of additives and high-performance fuel comprising such a composition|

---

TW104105510A| TW201540706A|2014-02-24|2015-02-17|Composition of additives and high-performance fuel comprising such a composition|

---

EA201691729A| EA201691729A1|2014-02-24|2015-02-17|COMPOSITION OF ADDITIVES AND HIGH-PRODUCTIVE FUEL CONTAINING THIS COMPOSITION|

---

EP15706411.4A| EP3110928A1|2014-02-24|2015-02-17|Composition of additives and performance fuel comprising such a composition|

---

CN201580010239.XA| CN106029844B|2014-02-24|2015-02-17|Compositions of additives and high performance fuel comprising the composition|

---

JP2016570177A| JP6456406B2|2014-02-24|2015-02-17|Additive composition and high performance fuel comprising such composition|

---

PCT/EP2015/053346| WO2015124584A1|2014-02-24|2015-02-17|Composition of additives and performance fuel comprising such a composition|

---

CA2939363A| CA2939363A1|2014-02-24|2015-02-17|Composition of additives and performance fuel comprising such a composition|

---

ARP150100528A| AR099522A1|2014-02-24|2015-02-23|COMPOSITION OF ADDITIVES AND HIGH PERFORMANCE FUEL THAT INCLUDES SUCH COMPOSITION|