WO2014046982A1 - Carburants et additifs pour carburant comprenant des dérivés d'ester de l'acide 5-méthyl-2-furoïque - Google Patents

Carburants et additifs pour carburant comprenant des dérivés d'ester de l'acide 5-méthyl-2-furoïque Download PDF

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Publication number
WO2014046982A1
WO2014046982A1 PCT/US2013/059836 US2013059836W WO2014046982A1 WO 2014046982 A1 WO2014046982 A1 WO 2014046982A1 US 2013059836 W US2013059836 W US 2013059836W WO 2014046982 A1 WO2014046982 A1 WO 2014046982A1
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WIPO (PCT)
Prior art keywords
fuel
molecules
formula
mixture
gasoline
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Application number
PCT/US2013/059836
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English (en)
Inventor
Aviad Cahana
Jeremy STANDIFORD
Peter Mikochik
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Xf Technologies Inc.
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Publication date
Application filed by Xf Technologies Inc. filed Critical Xf Technologies Inc.
Publication of WO2014046982A1 publication Critical patent/WO2014046982A1/fr
Priority to US14/503,450 priority Critical patent/US20150047251A1/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/023—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for spark ignition
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
    • C10L1/026—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/02—Use of additives to fuels or fires for particular purposes for reducing smoke development
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/08—Use of additives to fuels or fires for particular purposes for improving lubricity; for reducing wear

Definitions

  • the present invention concerns the use of molecules of Formula I (as shown in FIG. 1) as fuels and fuels additives, where R is hydrogen, alkyl, or aromatic, with between 1 to 10 carbon atoms, or combination of carbon, hydrogen, and oxygen and R[sub] l comprises alkyl or aromatic, with between 1 to 18 carbon atoms, or a combination of carbon, hydrogen, and oxygen.
  • Oxygenates are molecules containing atoms of oxygen, carbon and hydrogen that are used in the fuel and fuel add itives field to obtain certain desirable properties in the fuel blend.
  • the EPA had mandated the use of oxygenates in gasoline for many years specifically to reduce air pollution, in particular ground-level ozone, carbon monoxide (CO), and smog. (1970 CAA, 1990 CAAA, Energy Independence and Security Act of 2007 (Pub.L. 110-140).
  • Other performance enhancing properties are also associated with some oxygenates, such as increased octane rating and higher
  • Methyltertiary butylether for example, was used extensively in gasoline in the US to reduce emissions and increase octane (M. Winterberg, E. Schulte-Korne, U. Peters, F. N ierlich "Methyl Tert-Butyl Ether” in U llmann's Encyclopedia of Industrial Chemistry, 2010, Wiley-VCH, Weinheim. doi :10.1002/14356007.a l6_543.pub2).
  • MTBE Methyltertiary butylether
  • ethanol is limited to gasoline and even as a blended component in gasoline has some shortfalls.
  • alcohols such as methanol and ethanol tend to absorb water as a result of their polar hydrophilic character. Phase separation is commonly observed in a gasoline- alcohol blend once even a small amount of water is absorbed. This can result in the accelerated corrosion of a fuel system as well as plugging of fuel filters by the corrosion products.
  • increased wear from the fuel wetted components, such as fuel pumps, injectors, etc. is a known phenomenon. Extraordinary precautions must therefore be taken to avoid water contamination of alcohol- containing fuels.
  • CRC Project CM-136-09-1B CRC Report No. 664, CRC Report No. E-90, CRC REPORT NO. 662, Renewable Fuels Association: E15 Misfueling Mitigation Plan.
  • Another shortfall of ethanol is its comparatively low energy density, with regard to gasoline, a property that reduces the fuel economy of the vehicle.
  • Ethanol was tested heavily as a potential candidate to reduce particulate matter in diesel, but was shown to reduce the flash point to a level that renders the blend unusable in diesel engines. Due to its low energy content, the use of ethanol in jet fuel is generally not acceptable by the engine manufacturer. Other oxygenates showed similarly poor performance in both diesel jet fuels.
  • the present invention concerns the use of molecules of Formula I (as shown in FIG. 1) as fuels and fuels additives, where R is hydrogen, alkyl, or aromatic, with between 1 to 10 carbon atoms, or combination of carbon, hydrogen, and oxygen and R[sub] l comprises alkyl or aromatic, with between 1 to 18 carbon atoms, or a combination of carbon, hydrogen, and oxygen.
  • R[sub] l comprises an alkyl with between 1 and 18 carbon atoms as fuels and fuel additives.
  • Such derivatives had been shown to be made from renewable feedstock by Mikochik and Cahana (PCT/US2011/048009 CA2808842A1, EP2606039A1). Further, the major precursor for such derivatives can be made from cellulosic material on a commercial scale as described by Cahana and Zhang et al. in PCT application
  • molecules of formula I and II in addition to molecules of formula I and II as they are described herein being oxygenates, they can also be made to have energy density that is equal to or greater than that of gasoline, diesel and jet fuel. This and other properties allow the use of molecules I and II as fuels and/or fuel additives. In engine studies conducted with these molecules, it was found that the use of molecules of formula II in diesel allowed for reduction of about 50% in particulate matter as emitted directly from the engine. Another notable finding that is based in testing is the lubricity properties of molecules of formula II, which are particularly useful in diesel. In testing, it was found that by replacing 10% by volume of diesel with molecules of formula II where R[sub] l is an alkyl with 2 carbon atoms, the lubricity of the mixture was improved by 33%.
  • the present invention concerns the use of molecules of formula II as fuels and fuel additives in all types of internal combustion engines, external combustion engines and air-breathing combustion engines.
  • molecules of formula II can be used to displace crude oil products by providing the energy required for the work generated by the engine. That energy is released when molecules of formula II are combusted.
  • molecules of formula II can be used as an oxygenate, and to impart desirable properties to the fuel, such as increased combustion efficiency, improve lubricity, improve anti-knock properties, reduce harmful emissions, and/or increasing horsepower and torque.
  • Molecules of formula II can comprise up to 25% by volume of the fuel for spark ignition internal combustion engines (SI ICE) with little to no reduction in engine performance.
  • SI ICE spark ignition internal combustion engines
  • 75% to 99.99% of the fuel can be composed of typical fuel blends that are used in SI ICE, such as those used for transportation, recreation and general work, and which the properties of the mixture are referenced by standards such as ASTM D4814.
  • This fuel is commonly referred to as gasoline.
  • alcohols such as ethanol comprise some portion of the fuel blend
  • the volume of molecules of formula II can be adjusted such that the total oxygen content of the fuel mixture shall not exceed 8.3% by weight.
  • the use of molecules of formula II can lead to improved performance of the SI ICE, such as increase in fuel combustion efficiency.
  • Molecules of formula II that are particularly useful for this invention include those where R[sub] l is an alkyl with between 1 and 4 carbon atoms.
  • a further advantage of the present invention is that in a mixture comprising of molecules of formula II and gasoline fuel the Reid vapor pressure of the fuel is not adversely affected. That is, the Reid vapor pressure is desirably lowered. This is a distinct advantage since potentially low cost, highly volatile, fuel components such as butanes can then be blended into the fuel without exceeding the desired vapor pressure limit.
  • Fuel blends for S I ICE can comprise up to 100% of molecules of formula II with appropriate modifications to the engine and/or fuel systems.
  • a high compression and/or forced induction engine with appropriate fuel pumps and fuel injectors with higher mass flow rate can utilize a fuel comprising up to 100% of molecules of formula II.
  • Molecules of formula I I can comprise up to 100% by volume of the fuel for compression ignition internal combustion engines (CIICE) with little to no reduction in engine performance. In this case, 70% to 99.99% of the fuel will be composed of typical fuel blends that are used in CIICE, such as those used for transportation, recreation and general work, and which the properties of the mixture are referenced by standards such as ASTM D975. This fuel is commonly referred to as Diesel.
  • biodiesel fatty acid methyl esters
  • the use of molecules of formula I I as described herein also serves to reduce and/or limit particulate matter generation in CI ICE engines.
  • the lubricating properties of molecules of formula II can increase the useable life of the engine itself and/or components within the engine and/or the fuel systems.
  • Molecules of formula II that are particularly useful for this invention include those where R[sub] l is an alkyl with between 1 and 12 carbon atoms.
  • Molecu les of formu la I I can be used at up to 100% to provide the energy required for the engine to generate work in fuel blends that are typical for use with external combustion engines.
  • Molecules of formula I I can comprise up to 50% by volume of the fuel for air-breathing combustion engines with little to no reduction in engine performance.
  • 80% to 99.99% of the fuel can be composed of typical fuel blends that are used in air-breathing engines, such as those used for transportation, recreation and general work, and which the properties of the mixture are referenced by standards such as ASTM D1655, ASTM D7566.
  • This fuel is commonly referred to as Jet Fuel.
  • the use of molecules of formula I I as described herein also serves to reduce and/or limit particulate matter generation in air-breathing engines.
  • the lu bricating properties of molecules of formula II can increase the useable life of the engine itself and/or components within the engine and/or the fuel system.
  • Molecules of formula I I that are particularly useful for this invention include those where R[sub] l is an alkyl with between 1 and 12 carbon atoms.
  • FIG. 1 is a schematic illustration of the structure of molecules of formula I and formula II.
  • An example embodiment of the present invention provides a fuel blend comprising from about 6% to about 20% linear paraffins by volu me, from about 25% to about 47% branched paraffins by volume, from about 17% to about 50% alkylated benzenes by volume, about 10% ethanol by volume and about 16% by volume of molecules of formula II where R[sub] l is an alkyl with between 1 and 2 carbon atoms.
  • Such mixture will contain about 8.3% oxygen by weight, such that no modification to a common SI ICE engine is required.
  • crude oil products are displaced at about 26% by volume in favor of renewable fuels.
  • the performance of SI ICE engines burning this blend of fuels would not be compromised and can be significantly increased due to the higher octane rating and lower stoichiometric air/fuel ratio.
  • Emissions of harmful greenhouse gases such as carbon monoxide, ozone, etc. can be significantly reduced due to the relatively high percentage of oxygen (8.3 wt/wt%) in the fuel.
  • Another example embodiment of the present invention provides for a gasoline fuel blend comprising 25% of molecules of formula II where R[sub] l is either a methyl or ethyl group.
  • R[sub] l is either a methyl or ethyl group.
  • the Reid vapor pressure can be reduced while the octane rating can be increased.
  • This allows for the addition of lower cost gasoline components such as butane and linear (straight chain) paraffins.
  • a further advantage of such a blend is a decrease in evaporative emissions of
  • Another example embodiment of the present invention provides for a fuel blend comprising 100% of molecules of formula II where R[sub] l is an alkyl with between 1 and 4 carbon atoms.
  • Specially designed engines such as very high compression engines and/or forced induction engines can be required to burn this type of blend, but these engines can also have advantages over typical internal combustion engines. Namely, a higher compression ratio and/or high boost pressure from forced induction increases combustion efficiency and increases the horsepower and torque output of the engine. This can result in smaller engines with larger power output, reducing the weight of the vehicle resulting in increased miles per gallon, faster acceleration and better handling and drivability.
  • Material construction of the engine should tolerate the higher temperatures associated with a high compression ratio and/or forced induction.
  • An iron block engine can be suitable, but aluminum block engines might pose additional challenges.
  • Another example embodiment of the present invention provides for a Diesel fuel blend comprising of 90% conventional diesel fuel (75% saturated hydrocarbons, and 25% aromatic hydrocarbons) and 10% molecules of formula II by volume.
  • a CI ICE using this blend to produce power will produce ⁇ 50% particulate matter by mass than the same engine using conventional diesel.
  • the CI ICE using the 10% formula II (where R[sub] l is an alkyl with between 1 and 8 carbon atoms) blend will have a prolonged life due to the lubricity properties of the blend.
  • Another example embodiment of the present invention provide for a fuel blend comprising of 100% of molecules from formula II where R[sub] l is an alkyl with between 1 and 12 carbon atoms which can then co-burned with coal to generate steam to power a steam turbine engine for electricity.
  • a fuel blend comprising of 100% of molecules from formula II where R[sub] l is an alkyl with between 1 and 12 carbon atoms which can then co-burned with coal to generate steam to power a steam turbine engine for electricity.
  • Such a fuel can greatly reduce emissions of undesirable greenhouse gases while providing a clean, renewable, domestic fuel source for electricity.
  • Another example embodiment of the present invention provides for a fuel blend comprising of 15% of molecules of formula II where R[sub] l is an alkyl between 1 and 12 carbon atoms and 85% diesel in modern ships and boats.
  • Such vessels are commonly powered by either two stroke or four stroke diesel (compression-ignition engine) engines.
  • compression-ignition engine compression-ignition engine
  • the advantages of using such a blend in marine vehicles include the ability to reduce the amount of crude oil in the blend by 15% and to increase lubricity which can improve performance and the life of both two stroke and four stroke
  • Another example embodiment of the present invention provides for a fuel blend comprising of about 80% jet fuel such as jet-A, jet-Al, JP-8 or JP-5 by volume and about 20% molecules of formula II where R[sub] l is an alkyl with between 1 and 12 carbon atoms, by volume.
  • jet fuel such as jet-A, jet-Al, JP-8 or JP-5
  • molecules of formula II are used to displace crude oil products but also to reduce particulate matter emissions.
  • the high smoke point of molecules of formula II can serve to reduce the soot trail of military aircraft.
  • Another advantage of molecules of formula II, especially those where R[sub] l is an alkyl with between 3 and 12 carbon atoms, is the high energy density and low density of the final fuel blend.
  • Another example embodiment of the present invention provides for a fuel blend comprising of 80% gasoline by volume and 20% molecules of formula II where R[sub] l is an alkyl with between 1 and 4 carbon atoms for use by two stroke engines. Due to the high lubricity of molecules in formula II, the need for adding lubricating oil to the fuel mixture is eliminated.
  • Two-stroke engines often provide high power-to-weight ratio, usually in a narrow range of rotational speeds called the "power band," and, compared to 4-stroke engines, have a greatly reduced number of moving parts, are more compact and significantly lighter. Because of the advantages of two stroke engines, they were very popular in the United States until the EPA mandated more stringent emission controls in 1978 (taking effect in 1980) and in 2004 (taking effect in 2005 and 2010). These engines are still very popular around the world.
  • the example embodiment provided here can influence a resurgence in the use of two-stroke engines resulting in lower cost, more efficient two stroke engines that produce much less air pollution.
  • Another example embodiment of the present invention provides for a fuel blend comprising charcoal and molecules of formula II where R[sub] l is an alkyl with between 1 and 18 carbon atoms for use as a clean burning cooking fuel.
  • R[sub] l is an alkyl with between 1 and 18 carbon atoms for use as a clean burning cooking fuel.
  • Cooking fuels currently in use such as coal, kerosene, or biomass produce toxic carbon monoxide gas during the combustion process and, in the case of kerosene, present fire hazards due to the high flammability of kerosene.
  • molecules in formula II can be utilized in place of these fuels to reduce indoor air pollution as well as reduce fire hazards for people currently using liquid or solid fuels for cooking.

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  • 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)
  • Combustion & Propulsion (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Liquid Carbonaceous Fuels (AREA)

Abstract

La présente invention concerne des dérivés d'ester d'acides furoïques et, en particulier, de l'acide 5-méthyl-2-furoïque, pouvant être utilisés comme carburants ou additifs pour carburant. Ces esters peuvent être utilisés pour remplacer les produits du pétrole brut, comme l'essence, le diesel, le carburant pour moteur à réaction, etc. Quand ils sont utilisés comme additifs pour carburant, ces esters améliorent les performances des moteurs à combustion interne à allumage par étincelles et des moteurs à combustion interne à allumage par compression. En outre, des tests ont montré que ladite molécule est également capable d'améliorer les performances des moteurs aérobies.
PCT/US2013/059836 2010-08-19 2013-09-14 Carburants et additifs pour carburant comprenant des dérivés d'ester de l'acide 5-méthyl-2-furoïque WO2014046982A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US14/503,450 US20150047251A1 (en) 2010-08-19 2014-10-01 Fuels and fuel additives comprising ester derivatives of 5-methyl-2-furoic acid

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201261705082P 2012-09-24 2012-09-24
US61/705,082 2012-09-24
US201261714225P 2012-10-16 2012-10-16
US61/714,225 2012-10-16
US201361818418P 2013-05-01 2013-05-01
US61/818,418 2013-05-01

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
US13/817,452 Continuation-In-Part US8710250B2 (en) 2010-08-19 2011-08-17 Conversion of 5-(chloromethyl)-2-furaldehyde into 5-methyl-2-furoic acid and derivatives thereof
PCT/US2011/048009 Continuation-In-Part WO2012024353A1 (fr) 2010-08-19 2011-08-17 Conversion de 5-(chlorométhyl)-2-furaldéhyde en acide 5-méthyl-2-furoïque et dérivés de celui-ci

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US14/503,450 Continuation-In-Part US20150047251A1 (en) 2010-08-19 2014-10-01 Fuels and fuel additives comprising ester derivatives of 5-methyl-2-furoic acid

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WO2014046982A1 true WO2014046982A1 (fr) 2014-03-27

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014132178A3 (fr) * 2013-02-28 2014-12-04 Rhodia Operations Derives du furfural a titre de vehicule
WO2019143893A1 (fr) * 2018-01-19 2019-07-25 Q-Maxx Products Group, Inc. Compositions de nettoyage de métal comprenant des esters de furoate et leurs utilisations

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100077655A1 (en) * 2008-09-05 2010-04-01 Joanna Margaret Bauldreay Liquid fuel compositions
WO2012024353A1 (fr) * 2010-08-19 2012-02-23 Incitor Incorporated Conversion de 5-(chlorométhyl)-2-furaldéhyde en acide 5-méthyl-2-furoïque et dérivés de celui-ci

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100077655A1 (en) * 2008-09-05 2010-04-01 Joanna Margaret Bauldreay Liquid fuel compositions
WO2012024353A1 (fr) * 2010-08-19 2012-02-23 Incitor Incorporated Conversion de 5-(chlorométhyl)-2-furaldéhyde en acide 5-méthyl-2-furoïque et dérivés de celui-ci

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2014132178A3 (fr) * 2013-02-28 2014-12-04 Rhodia Operations Derives du furfural a titre de vehicule
WO2019143893A1 (fr) * 2018-01-19 2019-07-25 Q-Maxx Products Group, Inc. Compositions de nettoyage de métal comprenant des esters de furoate et leurs utilisations
JP2021511412A (ja) * 2018-01-19 2021-05-06 キューマックス プロダクツ グループ， インク．Ｑｍａｘｘ Ｐｒｏｄｕｃｔｓ Ｇｒｏｕｐ， Ｉｎｃ． フロ酸エステルを含む金属洗浄組成物及びその使用

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