EP4363533A2 - Brennstoffzusammensetzung reich an aromatischen verbindungen, paraffinen und ethern und deren verwendung in kraftfahrzeugen - Google Patents

Brennstoffzusammensetzung reich an aromatischen verbindungen, paraffinen und ethern und deren verwendung in kraftfahrzeugen

Info

Publication number
EP4363533A2
EP4363533A2 EP22751127.6A EP22751127A EP4363533A2 EP 4363533 A2 EP4363533 A2 EP 4363533A2 EP 22751127 A EP22751127 A EP 22751127A EP 4363533 A2 EP4363533 A2 EP 4363533A2
Authority
EP
European Patent Office
Prior art keywords
mass
composition according
ether
composition
paraffins
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP22751127.6A
Other languages
English (en)
French (fr)
Other versions
EP4363533B1 (de
Inventor
Lisa SERVE
Géraldine DELORME
Florent Picard
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
TotalEnergies Onetech SAS
Original Assignee
TotalEnergies Onetech SAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by TotalEnergies Onetech SAS filed Critical TotalEnergies Onetech SAS
Publication of EP4363533A2 publication Critical patent/EP4363533A2/de
Application granted granted Critical
Publication of EP4363533B1 publication Critical patent/EP4363533B1/de
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/18Organic compounds containing oxygen
    • C10L1/185Ethers; Acetals; Ketals; Aldehydes; Ketones
    • C10L1/1852Ethers; Acetals; Ketals; Orthoesters
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/02Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/023Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L10/00Use of additives to fuels or fires for particular purposes
    • C10L10/02Use of additives to fuels or fires for particular purposes for reducing smoke development
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/10Feedstock materials
    • C10G2300/1011Biomass
    • C10G2300/1014Biomass of vegetal origin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/16Hydrocarbons
    • C10L1/1608Well defined compounds, e.g. hexane, benzene
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L2200/00Components of fuel compositions
    • C10L2200/04Organic compounds
    • C10L2200/0461Fractions defined by their origin
    • C10L2200/0469Renewables or materials of biological origin
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L2230/00Function and purpose of a components of a fuel or the composition as a whole
    • C10L2230/22Function and purpose of a components of a fuel or the composition as a whole for improving fuel economy or fuel efficiency
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L2270/00Specifically adapted fuels
    • C10L2270/02Specifically adapted fuels for internal combustion engines
    • C10L2270/023Specifically adapted fuels for internal combustion engines for gasoline engines

Definitions

  • TITLE Composition of fuel rich in aromatic compounds, paraffins and ether, and its use in motor vehicles
  • the subject of the present invention is a fuel composition intended for vehicles comprising a spark-ignition engine (or gasoline engine), and which has advantageous properties.
  • a subject of the invention is also the use of such a composition for supplying a spark-ignition engine, both in a conventional vehicle, in particular an automobile, and in a competition vehicle.
  • Gasoline-type fuels that can be used in spark-ignition engines, in particular those of motor vehicles, must have sufficiently high octane numbers to avoid knocking phenomena.
  • the octane number measures the resistance to auto-ignition of a fuel used in a spark-ignition engine.
  • gasoline fuels marketed in Europe complying with the EN 228 standard, have a motor octane number (or MON, for Motor Octane Number) greater than 85 and a research octane number (or RON, of English Research Octane Number) of a minimum of 95. These fuels are suitable for the vast majority of automotive engines.
  • a high volumetric compression ratio is particularly desired.
  • One objective of the present invention is therefore to improve the performance of gasoline fuel compositions, in particular but not limited to fuel compositions intended for competition vehicles.
  • the objective is to increase the energy content of the fuel, which will lead to an increase in the power of the spark-ignition engine, whether it is atmospheric, turbocharged, hybrid or not, during the combustion of the gasoline fuel composition in engine.
  • compositions from bases and/or compounds of renewable origin, also called biobased compounds.
  • octane enhancing additives are typically added to gasoline type fuel compositions.
  • Organometallic compounds including in particular iron, lead or manganese are well known octane improvers.
  • TEL tetraethyl lead
  • Non-metal based octane improvers include oxygenates (e.g. ethers and alcohols) and aromatic amines.
  • oxygenates e.g. ethers and alcohols
  • aromatic amines suffer from various disadvantages.
  • NMA N-methylaniline
  • an aromatic amine must be used at a relatively high treat rate (1.5 to 2 wt.% additive/fuel base weight) to have a significant effect on fuel efficiency.
  • NMA can also be toxic.
  • document US-A-4812146 describes unleaded gasoline fuel compositions for competition engines which comprise at least four components chosen from butane, isopentane, toluene, MTBE (methyl tert -butyl ether) and an alkylate.
  • Document WO2010/014501 describes unleaded gasoline fuel compositions comprising at least 45% by volume of branched paraffins, at most 34% by volume of one or more mono- and di-alkylated benzenes, from 5 to 6% by volume at least one linear paraffin having from 3 to 5 carbon atoms (denoted C3-C5), one or more alkanols having from 2 to 4 carbon atoms (denoted C2-C4), in sufficient quantity to increase the AKI ( of the English Anti Knock Index) i.e. (RON+MON)/2 of at least 93.
  • These compositions are presented as having high torque and maximum power.
  • the subject of the present invention is therefore a fuel composition
  • a fuel composition comprising:
  • compositions are intended to supply spark-ignition engines (or gasoline engines).
  • the fuel compositions according to the invention have high RON (Research Octane Number) octane numbers.
  • the use of the composition according to the invention makes it possible to achieve higher engine power levels, at a constant fuel flow rate.
  • composition according to the invention also has significant advantages for uses other than in competition vehicles, such as, for example, so-called general public uses, in particular for light vehicles (or light vehicles). If necessary, it can meet the specifications of the EN 228 standard.
  • NOx nitrogen oxides
  • composition according to the invention can advantageously be, in whole or in part, prepared from bases and/or compounds of renewable origin, for example of plant origin.
  • the composition according to the invention may contain at least 50% by mass of one or more biobased bases, preferably at least 60% by mass, more preferentially at least 65% by mass and better still at least 70% in bulk of one or more biosourced bases.
  • the reduction in greenhouse gas emissions obtained by means of the fuel composition of the invention is at least 50%, compared to the reference fossil fuel defined in this Directive.
  • the invention also relates to the use of the composition according to the invention for supplying a spark-ignition engine.
  • the composition according to the invention is used as fuel for supplying a high-efficiency, high-power spark-ignition engine, preferably a motor racing vehicle engine.
  • CN compound denotes a compound containing N carbon atoms in its chemical structure.
  • composition according to the invention contains a mixture (i) of hydrocarbons containing: a) from 35 to 55% by mass of aromatic compounds; b) from 30 to 50% by mass of non-cyclic paraffins containing at least 5 carbon atoms; and c) from 5 to 15% by mass of naphthenes.
  • Such a mixture of hydrocarbons represents from 50 to 79% by mass, relative to the total mass of the fuel composition, preferably from 55 to 75% by mass, and more preferably from 60 to 70% by mass, relative to the total mass of the fuel composition.
  • the aromatic compound(s) (i)a) are preferably chosen from alkylbenzenes comprising from 7 to 12 carbon atoms.
  • alkyl-benzenes is meant in a manner known per se benzene derivatives in which one or more hydrogen atoms are replaced by one or more alkyl groups.
  • the aromatic compound or compounds may in particular be chosen from toluene (methylbenzene), ethylbenzene, xylenes (and in particular 1,2-dimethylbenzene or ortho-xylene, 1,3-dimethylbenzene or meta-xylene and 1 ,4-dimethylbenzene or para-xylene), 1-ethyl-3-methylbenzene, mesitylene (1,3,5-trimethylbenzene), 1-ethyl-3,5-dimethylbenzene, and mixtures of these compounds.
  • toluene methylbenzene
  • ethylbenzene ethylbenzene
  • xylenes and in particular 1,2-dimethylbenzene or ortho-xylene, 1,3-dimethylbenzene or meta-xylene and 1 ,4-dimethylbenzene or para-xylene
  • 1-ethyl-3-methylbenzene mesitylene (1,3,5-trimethylbenzene
  • mixtures of aromatic compounds and more particularly mixtures of alkyl-benzenes comprising from 7 to 10 carbon atoms such as methylbenzene, ethylbenzene, xylenes (and in particular 1,2-dimethylbenzene or ortho -xylene, 1,3-dimethylbenzene or meta-xylene and 1,4-dimethylbenzene or para-xylene), l-ethyl-3-methylbenzene, mesitylene (1,3,5-trimethylbenzene), and l -ethyl-3,5-dimethylbenzene.
  • the content of the aromatic compounds (i)a) ranges from 40 to 53% by mass, preferably from 45 to 52% by mass, relative to the mass of the mixture of hydrocarbons (i).
  • composition according to the invention also contains non-cyclic paraffins (i)b) containing at least 5 carbon atoms.
  • paraffins is meant, in a manner known per se, branched alkanes (also called iso-paraffins or iso-alkanes) and unbranched alkanes (also called n-paraffins or n-alkanes).
  • the paraffins are preferably chosen from those comprising from 5 to 12 carbon atoms, more preferably from 5 to 9 carbon atoms, and better still from 5 to 8 carbon atoms.
  • the paraffins can be chosen from n-paraffins (or normal-paraffins, i.e. linear alkanes) and iso-paraffins (i.e. branched alkanes).
  • mixtures of n-paraffins and iso-paraffins chosen from those described above, preferably comprising a major proportion of iso-paraffins, with a mass ratio of the amount of iso-paraffins on the quantity of n-paraffins greater than or equal to 3, preferably greater than or equal to 4 and better still comprised in the range going from 4 to 5.
  • the mixture of hydrocarbons (i) advantageously contains from 5 to 10% by mass of n-paraffins and from 20 to 45% by mass of iso-paraffins.
  • the content of paraffins (i)b) ranges from 32 to 45% by mass, more preferably from 35 to 42% by mass, relative to the mass of the mixture of hydrocarbons (i).
  • composition according to the invention also contains naphthenes
  • naphthenes is meant, in a manner known per se, cyclic alkanes (or cycloalkanes) containing from 5 to 10 carbon atoms.
  • the naphthenes are chosen from cyclic alkanes containing from 5 to 10 carbon atoms, and more preferably from 6 to 9 carbon atoms.
  • the content of naphthenes (i)c) ranges from 7 to 13% by mass, more preferably from 8 to 12% by mass, relative to the mass of the mixture of hydrocarbons (i).
  • the mixture of hydrocarbons (i) comes from vegetable raw materials.
  • the mixture (i) advantageously consists entirely of biosourced hydrocarbons.
  • the plant-based raw materials may for example be chosen from cereals (for example wheat, maize), rapeseed, sunflower, soya, palm oil, sugar cane, beet, waste wood, straw, bagasse, grape marc, used vegetable cooking oils, seaweed, materials lignocellulosic.
  • cereals for example wheat, maize
  • rapeseed sunflower
  • soya palm oil
  • sugar cane, beet waste wood, straw, bagasse, grape marc
  • used vegetable cooking oils seaweed
  • materials lignocellulosic are particularly preferred.
  • vegetable raw materials containing carbohydrates such as cereals, sugar cane, beets, wood waste, straw, bagasse, grape marc, lignocellulosic materials which may be derived of the timber industry.
  • so-called second-generation (2G) or advanced plant material is used, in particular plant material that is not in competition with the food resource.
  • the mixture of hydrocarbons (i) is preferably obtained by converting the plant material into alcohols containing 1 to 5 carbon atoms, preferably methanol and/or ethanol, which are converted into hydrocarbons in the presence of catalysts making it possible to dehydrate the alcohols and produce reaction intermediates which, catalytically, are then transformed into hydrocarbons.
  • composition according to the invention also contains at least one ether.
  • Ethers also called ether-oxides or alkoxy-alkyls, are compounds of formula R-O-R' , in which R and R' , identical or different, represent an alkyl radical.
  • the ether(s) are chosen from the compounds of formula R-O-R′, in which R and R′, which are identical or different, represent a C1 to C5 alkyl radical.
  • R represents a C1 or C2 alkyl radical and R′ represents a C3, C4 or C5 alkyl radical.
  • the oxygenated compound(s) (ii) are chosen from tertio-butyl methyl ether (MTBE), tertio-butyl ethyl ether (ETBE), tertio-amyl methyl ether (TAME), tert-amyl ethyl ether (TAEE), and mixtures of these compounds.
  • MTBE tertio-butyl methyl ether
  • ETBE tertio-butyl ethyl ether
  • TAME tertio-amyl methyl ether
  • TEE tert-amyl ethyl ether
  • ETBE tert-butyl ethyl ether
  • one or more ethers of vegetable origin, or bioethers are used.
  • the ether can be obtained in a renewable manner by using, for example, a renewable alcohol, and an olefin resulting from thermal or catalytic cracking or by steam cracking of a renewable charge.
  • Bioethers can for example be produced by reaction between an alcohol and a generally branched olefin. They can be produced from renewable raw materials (in particular vegetable raw materials) by using, for example, alcohols obtained by transformation (for example fermentation) of renewable raw materials, and olefins resulting from cracking (thermal cracking, catalytic, or steam cracking) of a renewable charge, or by dehydration of an alcohol.
  • the olefins are produced by steam cracking of bionaphtha which is a by-product resulting from the production of renewable diesel by deoxygenation and isomerization of triglycerides of plant origin.
  • the composition has a total content of ether(s) ranging from 20 to 40% by mass, preferably from 22 to 35% by mass, and better still from 25 to 35% by mass, relative to the total mass of the fuel composition.
  • composition according to the invention also contains butane, which can be chosen from n-butane (linear butane), iso-butane (2-methylpropane) and mixtures of these two compounds.
  • Butane can be made from renewable raw materials. It can for example be obtained by fractionation of light hydrocarbons produced by catalytic cracking during the production of renewable gas oil which is obtained by deoxygenation and isomerization of triglycerides of vegetable origin, animal fats or waste cooking oils.
  • the composition has a butane content ranging from 1 to 10% by mass, preferably from 1.5 to 8% by mass, and better still from 2 to 6% by mass, relative to the total mass of the fuel composition .
  • the composition according to the invention comprises at most 2.5% by mass of olefins, preferably at most 2% by mass of olefins, more preferably at most 1% by mass of olefins, more preferably still at most 0.5% by mass of olefins.
  • the composition as described above generally has a research octane number (RON index) greater than or equal to 95, preferably greater than or equal to 99, and more preferably greater than or equal to 100, the RON being measured according to the standard ASTM D 2699-86.
  • the values above relate to the intrinsic octane number of the composition, that is to say without the addition of additional compounds such as in particular octane booster additives.
  • composition according to the invention may also contain one or more alcohols, preferably chosen from C1 to C6 alcohols, more preferably from C1 to C4 alcohols.
  • alcohols from renewable raw materials, and in particular of plant origin also called bioalcohols, are used.
  • Such alcohols may be present in the composition according to the invention in a content ranging from 1 to 10% by mass, preferably from 2 to 8% by mass.
  • the fuel composition according to the invention may also comprise one or more additives, chosen from among those usually employed in gasoline fuels.
  • composition according to the invention may comprise at least one detergent additive ensuring the cleanliness of the engine.
  • an additive may for example be chosen from the group consisting of succinimides optionally substituted with a polyisobutylene group, polyetheramines, betaines, Mannich bases and quaternary ammonium salts, for example those described in documents US4171959 and WO2006135881 .
  • the composition may also comprise at least one lubricity additive or anti-wear agent, in particular (but not limited to) chosen from the group consisting of fatty acids and their ester or amide derivatives, in particular glycerol monooleate, and derivatives of mono- and polycyclic carboxylic acids.
  • lubricity additive or anti-wear agent in particular (but not limited to) chosen from the group consisting of fatty acids and their ester or amide derivatives, in particular glycerol monooleate, and derivatives of mono- and polycyclic carboxylic acids.
  • lubricity additive or anti-wear agent in particular (but not limited to) chosen from the group consisting of fatty acids and their ester or amide derivatives, in particular glycerol monooleate, and derivatives of mono- and polycyclic carboxylic acids. Examples of such additives are given in the following documents: EP680506, EP860494, WO98/04656, EP915944, FR2772783, FR2772784.
  • additives may also be incorporated into the fuel composition according to the invention, such as anti-recession valve additives, antioxidant additives, additives increasing the octane number, in particular chosen from amines, preferably aromatic, with or without oxygen.
  • the additives described above can be added to the fuel composition in an amount ranging, for each of them, from 10 to 5000 ppm by mass, preferably from 50 to 1000 ppm by mass and better still from 100 to 500 ppm by mass, based on the total mass of the fuel composition.
  • the composition comprises at least one additive, advantageously chosen from detergent additives, lubricity additives, anti-recession valve additives, antioxidant additives, additives increasing the octane number , and mixtures of such additives.
  • the fuel compositions according to the invention have a lead content generally less than or equal to 5 mg/L (present for example in the form of tetraethyl lead) and, preferably, are lead-free, that is to say they do not contain lead or compounds containing lead. They are also free of sulfur (maximum content of 10 ppm by weight).
  • composition according to the invention can be prepared by simple mixing of its constituents.
  • a second non-limiting embodiment comprises the following steps:
  • butane optional addition of butane, such that the amount of butane in the final mixture is in the range of 1 to 10% by mass.
  • the base B is advantageously a biosourced base, that is to say that it is advantageously obtained from alcohols resulting from the fermentation of vegetable raw materials, and preferably vegetable raw materials containing carbohydrates, such as cereals, sugar cane, beets, wood waste, bakery waste, straw, bagasse, grape pomace, ligno-cellulosic materials.
  • Such vegetable raw materials can be converted into biohydrocarbons by known catalytic conversion methods.
  • the ether(s) are preferably bioethers.
  • the composition according to the invention can be prepared entirely from raw materials of renewable origin.
  • a subject of the invention is also the use of the composition as described above for supplying a spark-ignition engine.
  • the engine can be of the direct injection or indirect injection type.
  • the fuel composition can be advantageously used both to supply an engine of a conventional motor vehicle (known as "general public") and a high-efficiency, high-power spark-ignition engine, such as a competition vehicle engine automobile. It may be in particular an atmospheric or turbocharged engine used in a competition vehicle (circuits or rallies), or even a hybrid engine, that is to say a heat engine coupled to an electric motor.
  • the invention also relates to the use of the composition as described above for reducing greenhouse gas emissions, determined in accordance with EU Directive 2018/2001 of the European Parliament and of the Council of December 1, 2018 on the promotion of the use of energy produced from renewable sources.
  • EU Directive 2018/2001 of the European Parliament and of the Council of December 1, 2018 on the promotion of the use of energy produced from renewable sources.
  • the reduction of greenhouse gas emissions is determined in relation to a reference fossil fuel.
  • the method for calculating the reduction percentage is more specifically defined in Annex V, Part C of the Directive.
  • the reduction in greenhouse gas emissions obtained by means of the fuel composition of the invention is at least 50%, preferably at least 60% and even more preferably at least 65%, compared to the reference fossil fuel defined in the Directive.
  • Base B has the following composition: [Table 1]
  • a fuel composition C according to the invention was prepared, by mixing:
  • Fuel C according to the invention containing a biosourced base in a very large proportion as well as ETBE, made it possible to obtain satisfactory performance in terms of lower calorific value (PCI), and octane number (RON).
  • PCI calorific value
  • RON octane number

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Combustion & Propulsion (AREA)
  • Liquid Carbonaceous Fuels (AREA)
EP22751127.6A 2021-07-02 2022-07-01 Brennstoffzusammensetzung reich an aromatischen verbindungen, paraffinen und ethern und deren verwendung in kraftfahrzeugen Active EP4363533B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR2107178A FR3119625B1 (fr) 2021-07-02 2021-07-02 Composition de carburant riche en composés aromatiques, en paraffines et en éther, et son utilisation dans des véhicules automobiles
PCT/FR2022/051318 WO2022208038A2 (fr) 2021-07-02 2022-07-01 Composition de carburant riche en composés aromatiques, en paraffines et en éther, et son utilisation dans des véhicules automobiles

Publications (2)

Publication Number Publication Date
EP4363533A2 true EP4363533A2 (de) 2024-05-08
EP4363533B1 EP4363533B1 (de) 2025-02-19

Family

ID=77021631

Family Applications (1)

Application Number Title Priority Date Filing Date
EP22751127.6A Active EP4363533B1 (de) 2021-07-02 2022-07-01 Brennstoffzusammensetzung reich an aromatischen verbindungen, paraffinen und ethern und deren verwendung in kraftfahrzeugen

Country Status (9)

Country Link
US (1) US11802252B2 (de)
EP (1) EP4363533B1 (de)
JP (1) JP7629118B2 (de)
CN (1) CN117642491A (de)
BR (1) BR112023027100A2 (de)
ES (1) ES3025153T3 (de)
FR (1) FR3119625B1 (de)
PL (1) PL4363533T3 (de)
WO (1) WO2022208038A2 (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12606757B2 (en) 2023-10-02 2026-04-21 Turn 3 Holdings LLC Alcohol based unleaded automotive racing fuel

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1257865A (fr) * 1959-03-16 1961-04-07 Shell Int Research Composition carburante
US4171959A (en) 1977-12-14 1979-10-23 Texaco Inc. Fuel composition containing quaternary ammonium salts of succinimides
US4812146A (en) 1988-06-09 1989-03-14 Union Oil Company Of California Liquid fuels of high octane values
JPH06128570A (ja) * 1992-10-14 1994-05-10 Nippon Oil Co Ltd 無鉛高オクタン価ガソリン
GB9301119D0 (en) 1993-01-21 1993-03-10 Exxon Chemical Patents Inc Fuel composition
FR2751982B1 (fr) 1996-07-31 2000-03-03 Elf Antar France Additif d'onctuosite pour carburant moteurs et composition de carburants
US5730029A (en) 1997-02-26 1998-03-24 The Lubrizol Corporation Esters derived from vegetable oils used as additives for fuels
FR2772784B1 (fr) 1997-12-24 2004-09-10 Elf Antar France Additif d'onctuosite pour carburant
FR2772783A1 (fr) 1997-12-24 1999-06-25 Elf Antar France Additif d'onctuosite pour carburant
FI20021596A7 (fi) * 2002-09-06 2004-03-07 Neste Oil Oyj Dieselmoottorin polttoainekoostumus
JP4585175B2 (ja) 2003-03-20 2010-11-24 Jx日鉱日石エネルギー株式会社 ガソリン
AU2006257823B2 (en) 2005-06-16 2011-09-08 The Lubrizol Corporation Quaternary ammonium salt detergents for use in fuels
DE102007035500A1 (de) * 2007-07-28 2009-01-29 Andreas Stihl Ag & Co. Kg Kraftstoffzusammensetzung
DE102008008818A1 (de) * 2008-02-12 2009-08-20 Deutsche Bp Ag Kraftstoffe für Otto-Motoren
US20100018112A1 (en) 2008-07-28 2010-01-28 Joseph Michael Russo High octane unleaded fuel compositions and methods for increasing the maximum torque output value produced burning same
FR2987369A1 (fr) 2012-02-27 2013-08-30 Total Raffinage Marketing Composition de carburant liquide de forte puissance pour moteurs a allumage commande
FR3080382B1 (fr) * 2018-04-23 2020-03-27 Total Marketing Services Composition de carburant a forte puissance et effet fuel eco
FI129423B (en) * 2018-12-14 2022-02-15 Neste Oyj Diesel fuel composition

Also Published As

Publication number Publication date
US20220389340A1 (en) 2022-12-08
WO2022208038A3 (fr) 2022-11-24
FR3119625B1 (fr) 2023-02-17
ES3025153T3 (en) 2025-06-06
JP7629118B2 (ja) 2025-02-12
US11802252B2 (en) 2023-10-31
FR3119625A1 (fr) 2022-08-12
CN117642491A (zh) 2024-03-01
EP4363533B1 (de) 2025-02-19
BR112023027100A2 (pt) 2024-03-12
PL4363533T3 (pl) 2025-06-09
WO2022208038A2 (fr) 2022-10-06
JP2024523682A (ja) 2024-06-28

Similar Documents

Publication Publication Date Title
EP2820111B1 (de) Leistungsstarke flüssigbrennstoffzusammensetzung für ottomotoren
EP4330354A1 (de) Kraftstoffzusammensetzung reich an aromatischen verbindungen, paraffinen und ethanol und verwendung davon, insbesondere in wettkampffahrzeugen
EP3784760A1 (de) Hochleistungsfähige und umweltfreundliche brennstoffzusammensetzung
EP4363533B1 (de) Brennstoffzusammensetzung reich an aromatischen verbindungen, paraffinen und ethern und deren verwendung in kraftfahrzeugen
EP4544005B1 (de) Kraftstoffzusammensetzung mit geringer auswirkung auf co2-emissionen und verwendung davon, insbesondere in neuen fahrzeugen
WO2023218148A1 (fr) Composition de carburant à faible impact en émissions de co2 et son utilisation notamment dans des véhicules neufs
WO2022229579A1 (fr) Composition de carburant riche en composés aromatiques et en composés oxygénés
TWI254074B (en) Manufacturing method of alkylated biomass diesel fuel and product thereof
US12227711B2 (en) Formulation and cetane improvement based on organic nitrates for alcohol-based renewable diesel fuel
WO2025133517A1 (fr) Utilisation d'une composition de carburant renouvelable pour l'injection pilote dans un moteur a carburation mixte
WO2025109286A1 (fr) Carburant pour moteur a base d'un melange d'alcool et d'eau et contenant un additif d'amelioration de la combustion
WO2024189291A1 (fr) Carburant pour moteur a compression
FR3163952A1 (fr) Composition pour combustible marin comprenant de l’huile de pneus et un composant d’origine renouvelable
CN119391462A (zh) 一种可持续无铅航空汽油燃料组合物及其制备方法
FR3142763A1 (fr) Composition de carburant comprenant une base renouvelable et un composé phénolique et un composé aromatique hétérocyclique azoté
BR102022003667A2 (pt) Formulação de combustível renovável aplicado em ciclo diesel e baseada em álcoois

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: UNKNOWN

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20240110

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20240513

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20241017

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

Free format text: NOT ENGLISH

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602022010910

Country of ref document: DE

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: LANGUAGE OF EP DOCUMENT: FRENCH

REG Reference to a national code

Ref country code: NL

Ref legal event code: FP

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 3025153

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20250606

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250519

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PL

Payment date: 20250624

Year of fee payment: 4

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250519

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250619

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250620

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250520

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20250721

Year of fee payment: 4

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20250828

Year of fee payment: 4

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20250722

Year of fee payment: 4

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20250731

Year of fee payment: 4

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 20250721

Year of fee payment: 4

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20250725

Year of fee payment: 4

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20250219

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602022010910

Country of ref document: DE

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

REG Reference to a national code

Ref country code: CH

Ref legal event code: L10

Free format text: ST27 STATUS EVENT CODE: U-0-0-L10-L00 (AS PROVIDED BY THE NATIONAL OFFICE)

Effective date: 20251231

26N No opposition filed

Effective date: 20251120

REG Reference to a national code

Ref country code: CH

Ref legal event code: H13

Free format text: ST27 STATUS EVENT CODE: U-0-0-H10-H13 (AS PROVIDED BY THE NATIONAL OFFICE)

Effective date: 20260224

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20250701