WO2007104514A2 - Method for the synthesis of 5-alkoxymethyl furfural ethers and their use - Google Patents

Method for the synthesis of 5-alkoxymethyl furfural ethers and their use Download PDF

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WO2007104514A2
WO2007104514A2 PCT/EP2007/002145 EP2007002145W WO2007104514A2 WO 2007104514 A2 WO2007104514 A2 WO 2007104514A2 EP 2007002145 W EP2007002145 W EP 2007002145W WO 2007104514 A2 WO2007104514 A2 WO 2007104514A2
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glucose
acid
flow process
continuous flow
ethanol
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PCT/EP2007/002145
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French (fr)
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WO2007104514A3 (en
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Gerardus Johannes Maria Gruter
F. Dautzenberg
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Furanix Technologies B.V.
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Priority to NZ571517A priority Critical patent/NZ571517A/en
Priority to AT07723190T priority patent/ATE497956T1/en
Priority to KR1020087024723A priority patent/KR101449731B1/en
Priority to EP07723190A priority patent/EP2004620B1/en
Priority to CN2007800083553A priority patent/CN101400666B/en
Priority to CA2644409A priority patent/CA2644409C/en
Priority to AP2008004633A priority patent/AP2008004633A0/en
Priority to BRPI0707100-0A priority patent/BRPI0707100A2/en
Priority to MX2008011592A priority patent/MX2008011592A/en
Application filed by Furanix Technologies B.V. filed Critical Furanix Technologies B.V.
Priority to JP2008558697A priority patent/JP5738517B2/en
Priority to AU2007224707A priority patent/AU2007224707B2/en
Priority to DE602007012422T priority patent/DE602007012422D1/en
Priority to EA200870340A priority patent/EA021670B1/en
Priority to US12/282,264 priority patent/US8133289B2/en
Publication of WO2007104514A2 publication Critical patent/WO2007104514A2/en
Priority to UAA200811994A priority patent/UA98455C2/en
Publication of WO2007104514A3 publication Critical patent/WO2007104514A3/en
Priority to ZA2008/08367A priority patent/ZA200808367B/en
Priority to US12/968,378 priority patent/US8877950B2/en
Priority to US13/314,618 priority patent/US8338626B2/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40—Radicals substituted by oxygen atoms
    • C07D307/46—Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
    • 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
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/10—Process efficiency

Definitions

  • the present invention relates to a method for the preparation of derivatives of 5-hydroxymethylfurfural (HMF) , in particular ether derivatives of HMF, more in particular to 5-alkoxymethylfurfural ethers and to their application as a fuel or fuel additive.
  • HMF 5-hydroxymethylfurfural
  • sugars or sugar (hexoses) containing biomass into more economically useful compounds is of increasing interest.
  • Current fuel activities are mainly directed towards ethanol from sugar/glucose.
  • sucrose and glucose are fermented into ethanol.
  • One glucose molecule is converted into two molecules of ethanol and two molecules of C02. This conversion has drawbacks especially in view of atom economy, the low energy density of ethanol (7.7 kWh/kg or 6.1 kWh/L) and its relative low boiling point (78,4 degrees Celsius) .
  • HMF is obtained as a highly potential starting material for obtaining bio-based monomer such as furandicarboxylic acid which can inter alia be used as an alternative to terephthalic acid as a monomer for polyethylene terephthalate type polyesters (Moreau et . al . in Topics in Catalysis VoI 27, Nos . 1-4, 2004, 11 - 30 and references cited therein) .
  • the inventors have found that the conversion of hexose-containing starting material, in particular fructose and/or glucose -containing starting material and more particular glucose- containing material that may be derived from biomass in the presence of a catalytic or sub-stoechiometric amount of acid in the presence of an alcohol with or without the presence of one or more additional diluents leads to the formation of the corresponding HMF-ether in good yield and selectivity.
  • the invention pertains to a method for the manufacture of 5-alkoxymethylfurfural ethers by reacting a fructose and/or glucose-containing starting material with an alcohol in the presence of a catalytic or sub-stoechiometric amount of acid catalyst.
  • the energy density of 5 -ethoxymethylfurfural (EMF) the ether resulting from reaction of HMF with (bio) ethanol, can be calculated.
  • EMF 5 -ethoxymethylfurfural
  • the reaction enthalpy can be calculated as 3854.76 kJ/mol, leading to an energy density of 7.0 kWh/kg or 8.7 kWh/L. This is as good as regular gasoline (12.7 kWh/kg, 8.8 kWh/L) and diesel ((11.7 kWh/kg, 9.7 kWh/L) and significantly higher than ethanol (7.7 kWh/kg, 6.1 kWh/L) .
  • the alcohol is selected from the group consisting of primary (un) branched aliphatic alcohols.
  • the alcohol is selected from the group consisting of primary C1-C5 (un) branched aliphatic alcohols, preferably methanol, ethanol, 1-propanol, 2-hydroxymethyl-propanol, 1-butanol.
  • methanol and/or ethanol More preferable are methanol and/or ethanol.
  • the resulting (m) ethyl ether (m) ethoxymethy1furfural, MMF or EMF) has a high energy content and may directly be used as a fuel additive as an alternative for MTBE or as a fuel. Mixtures of alcohols may also be employed.
  • Ethanol is the most preferred alcohol in the method of the present invention as the ethanol that is used can also be derived from biomass or glucose-containing material (bio-ethanol) .
  • the acid catalyst in the method of the present invention can be selected from amongst (halogenated) organic acids, inorganic acids, salts, Lewis acids, ion exchange resins and zeolites or combinations and/or mixtures thereof .
  • the acid catalyst is a heterogeneous catalyst.
  • the acid catalyst is a homogenous catalyst.
  • the acid may be a protonic, Br ⁇ nsted or, alternatively, a Lewis acid.
  • the acid may be organic or inorganic.
  • the organic acid can be selected from amongst oxalic acid, levulinic acid, maleic acid or para-toluenesulphonic acid.
  • the inorganic acid can be selected from amongst phosphoric acid, sulphuric acid, hydrochloric acid, hydrobromic acid, nitric acid, hydroiodic acid, optionally generated in situ. In certain embodiments, the inorganic acid is selected form the group of sulphuric acid, phosphoric acid, hydrochloric acid, nitric acid.
  • the salt can be one of (NH4) 2SO4/SO3 , ammonium phosphate, triethylamine phosphate, pyridinium salts, pyridinium phosphate, pyridinium hydrochloride/hydrobromide/perbromate, DMAP, aluminium salts, Th and Zr ions, zirconium phosphate, Cr-, Al-, Ti-, Ca-, In-ions, ZrOC12, VO(SO4)2, TiO2 , V-porphyrine, Zr-, Cr-, Ti- porphyrine .
  • the Lewis acid can be one of ZnCL2 , A1C13, BF3.
  • the ion exchange resins can be one of Amberlite, Diaion, levatit.
  • the acid catalyst is a solid catalyst that may be selected form the group consisting of acid resins, natural clay- mineral, zeolites, supported acids such as silica impregnated with mineral acids, heat treated charcoal, metal oxides, metal sulfides, metal salts and mixed oxides and mixtures thereof. In certain embodiments, mixtures or combinations of acid catalysts can be used.
  • the temperature at which the reaction is performed may vary, but in general it is preferred that the reaction is carried out at a temperature from 50 to 300 degrees Celsius, preferably from 125 to 250, more preferably from 175 to 225 degrees Celsius. In general, temperatures higher than 300 are less preferred as the selectivity of the reaction as many by-products occur, inter alia caramelisation of the sugar. Performing the reaction below the lowest temperature is also less preferable because of the slow reaction speed.
  • the fructose and/or glucose-containing starting material can be selected from a wide variety of feeds. In general any feed with a sufficient high fructose or glucose content can be used. It is preferred that the fructose and/or glucose -containing starting material is selected from the group of starch, amylose, galactose, cellulose, hemi-cellulose, glucose-containing disaccharides such as sucrose, maltose, cellobiose, lactose, preferably glucose-containing disaccharides, more preferably sucrose or glucose.
  • the catalyst can be added to the reaction mixture in an amount varying from 0.01 to 40 mole % drawn on the fructose or glucose content of the fructose and/or glucose -containing starting material preferably from 0.1 to 30 mole %, more preferably from 1 to 20 mole %.
  • one or more solvents or diluents may be added, in general to aid the dissolution of the glucose containing material or as a diluent.
  • the solvent may be selected form the group consisting of water, sulfoxides, preferably DMSO, ketones, preferably methyl ethylketone, methylisobutylketone and acetone or mixtures of two or more of the above solvents .
  • the ratio of alcohol/solvent is from 50 to 0.1, preferably from 20 to 1, more preferably from 10 to 2. Higher amounts of alcohol may have the result that the reaction is too slow due to the limited solubility (hence availability of the starting material) , whereas too much solvent in the system may lead to a too high dilution, which in both cases are less preferred results.
  • One of the possible solvents is water.
  • the method can be performed in a continuous flow process. In such method, homogenous catalysts may be used and the residence time of the reactants in the flow process is between 0.1 second and 10 hours, preferably from 1 second to 5 hours, more preferably from 1 minute to 1 hour.
  • the continuous flow process is a fixed bed continuous flow process or a reactive (catalytic) distillation process with preferably a heterogeneous acid catalyst.
  • a reactive (catalytic) distillation process with preferably a heterogeneous acid catalyst.
  • an inorganic or organic acid may be added to the feed of the fixed bed or reactive distillation continuous flow process.
  • the liquid hourly space velocity (LHSV) can be from 1 to 1000, preferably from 5 to 500, more preferably from 10 to 250 and most preferably from 25 to 100.
  • the application of the products of the method of the present invention i.e. the ethers, is in the use as a fuel or fuel additive and as precursor for the manufacture of 2,5- di (hydroxymethyl) furan, furan-2, 5-dicarboxylic acid, 2- hydroxymethylfuran-5-carboxylic acid, 2,5-
  • Example 1 In a continuous flow reactor, sucrose 10 mmol/1, dissolved in water/ethanol/10% H2SO4, was reacted at a temperature of 195 degrees Celsius with a residence time between 6 and 60 seconds and a flow rate of 10 ml/min, i.e. 3.33 ml/min/reactor . At 6 seconds, mainly conversion into fructose and glucose was observed, but at prolonged residence times, 2 main furan peaks were observed in the UV spectrum. Mass spectrometry identified these products as HMF and EMF with a selectivity of >90 % at a conversion of 25%.
  • Example 2 In a continuous flow reactor, glucose 10 mmol/1, dissolved in water/ethanol/10% H2SO4, was reacted at a temperature of 195 degrees Celsius with a residence time between 6 and 60 seconds and a flow rate of 10 ml/min, i.e. 3.33 ml/min/reactor . At 30 seconds, 2 main furan peaks were observed in the UV spectrum. Mass spectrometry identified these products as HMF and EMF with a selectivity of >90 % at a conversion of 10%.
  • Continuous parallel flow reactor system consisting of four quartz reactors inserted in a silver heating block; temperature and flow regulators and three HPLC pumps. Two of the pumps deliver the liquid to the reactors and third one is employed to dilute the reaction products prior to collection.
  • reaction products were quantified with the aid of HPLC-analysis with an internal standard (saccharine, Sigma Aldrich) .
  • an internal standard sacharine, Sigma Aldrich
  • a 1.25 wt% solution of glucose (99.7 % Sigma Aldrich) in water or 88.7 % ethanol was flowed through a fixed bed (200 ⁇ l) of a heterogeneous catalyst at 180 0 C. Flow rates were chosen such to achieve a space velocity 0.25 or 0.5 min "1 , i.e. contact time 2 or 4 tnin. Liquid coming out of the reactors was diluted by a mixture of water and ethanol (50:50) to prevent tubing blockages.
  • Catalysts tested Catalyst 1 Zeolite beta SAR25 (CBV Zeolyst)
  • Catalyst 2 Zeolite Y high SAR CBV Zeolyst
  • Catalyst 2 Zeolite Y high SAR CBV Zeolyst
  • Figure 1 a) and b) show that a conversion achieved for the catalysts tested was 76% (Zeolite beta) . This catalyst gave 7% selectivity to HMF and EMF.
  • Zeolite Y with high SAR presented 9% selectivity to furans at 20% conversion.
  • Y zeolite with low SAR shows selectivity of 4% at very low conversion.
  • Mordenite presented both reduced activity and selectivity to furan derivatives. HMF was a main furan found in the reaction mixture.
  • the predominant furan derivative was the desired EMF.
  • a small-scale model diesel engine comparative testing is performed with normal commercial diesel as a fuel and the same commercial diesel to which samples of 1 wt.%, 2 wt.%, 3 wt.%, 5 wt%, and 10 wt.% HMF or EMF are added, respectively.
  • the diesel samples with HMF are less homogenous on visual inspection (solid particles remain visible, flocculation) and above 5 wt.% HMF, a solid deposit is sometimes observed.
  • EMF is added as a liquid and does not yield any mixing or flocculation problems.
  • the engine is run stationary with a set volume (100 mL) of fuel until empty. HMF containing fuels run less regular, whereas EMF containing fuels run at a regular pace and for a longer period (up to 15%) . On visual inspection of the engine, EMF provides less visual contamination.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Furan Compounds (AREA)
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Abstract

Method for the manufacture of 5-alkoxymethyl furfural derivatives by reacting a fructose and/or glucose-containing starting material with an alcohol in the presence of a catalytic or sub-stoechiometric amount of heterogeneous acid catalyst. The catalysts may be employed in a continuous flow fixed bed or catalytic distillation reactor. The ethers can be applied as a fuel or fuel additive.

Description

Title: Method for the synthesis of 5 -alkoxymethylfurfural ethers and their use.
The present invention relates to a method for the preparation of derivatives of 5-hydroxymethylfurfural (HMF) , in particular ether derivatives of HMF, more in particular to 5-alkoxymethylfurfural ethers and to their application as a fuel or fuel additive.
The conversion of sugars or sugar (hexoses) containing biomass into more economically useful compounds is of increasing interest. Current fuel activities are mainly directed towards ethanol from sugar/glucose. Typically, sucrose and glucose are fermented into ethanol. One glucose molecule is converted into two molecules of ethanol and two molecules of C02. This conversion has drawbacks especially in view of atom economy, the low energy density of ethanol (7.7 kWh/kg or 6.1 kWh/L) and its relative low boiling point (78,4 degrees Celsius) .
Another application area involves the conversion of sugars such as fructose into HMF in the presence of an acid catalyst has been reported (for example in EP0230250 to Suedzucker or EP0561928 to CEA) ) . In this case HMF is obtained as a highly potential starting material for obtaining bio-based monomer such as furandicarboxylic acid which can inter alia be used as an alternative to terephthalic acid as a monomer for polyethylene terephthalate type polyesters (Moreau et . al . in Topics in Catalysis VoI 27, Nos . 1-4, 2004, 11 - 30 and references cited therein) . When under these conditions sucrose or glucose was used as a feed, no conversion to HMF is observed (Moreau et . al . in Topics in Catalysis VoI 27, Nos. 1-4, 2004, pl3, col 2. line 2-3), which is a distinct disadvantage given the low price and abundant availability of sucrose and glucose. Only in the presence of DMSO, DMF and DMA (low HMF yields from glucose: Ishida et . al . Bull. Chem. Soc . Jpn 74 2001, 1145) or in a sub- and supercritical mixture of acetone and water (fructose, glucose, sucrose and inulin conversion to HMF in 77%, 48%, 56% and 78% yields respectively: Vogel et . al . Green Chemistry 5, 2003, 280) reasonable HMF yields from starting materials other than fructose were obtained.
In the current market situation, fructose as feed is undesirable given the high price thereof, compared to glucose and/or sucrose. Therefore, so far, no process for the synthesis of HMF has been developed on an industrial scale .
The synthesis chemistry and applications of HMF are reviewed extensively in Lewkowski, ARKIVOC 2001, (i) 17-54; in Gandini, Prog. Polym. Sci. 22, 1997, 1203; in Lichtenthaler, CR. Chimie, 7, 2004, 65 and Ace. Chem. Res. 35, 2002, 728; and Moreau, Topics in Catalysis, 27, 2004, 11.
Concluding, the current methods for the synthesis of HMF mostly start from fructose and typically do not give high yield, partly attributable to the instability of HMF under the acidic reaction conditions. In most acid-catalysed water-based reactions, the further reaction to levulinic acid and humins has been reported, making this a less attractive alternative.
The present inventors have set out to overcome these disadvantages.
Surprisingly, the inventors have found that the conversion of hexose-containing starting material, in particular fructose and/or glucose -containing starting material and more particular glucose- containing material that may be derived from biomass in the presence of a catalytic or sub-stoechiometric amount of acid in the presence of an alcohol with or without the presence of one or more additional diluents leads to the formation of the corresponding HMF-ether in good yield and selectivity.
Thus, the invention pertains to a method for the manufacture of 5-alkoxymethylfurfural ethers by reacting a fructose and/or glucose-containing starting material with an alcohol in the presence of a catalytic or sub-stoechiometric amount of acid catalyst.
It was found that this in situ formation and derivatisation of HMF prevents the occurrence of the onward and undesired reaction towards the above-mentioned levulinic acid and humins, thus leading to an efficient procedure for the conversion of fructose and/or glucose -containing material into HMF derivatives.
The energy density of 5 -ethoxymethylfurfural (EMF) , the ether resulting from reaction of HMF with (bio) ethanol, can be calculated. Taking into account stoeichiometry and a calculated enthalpy of formation using increment tables of 502.32 kJ/mole, the reaction enthalpy can be calculated as 3854.76 kJ/mol, leading to an energy density of 7.0 kWh/kg or 8.7 kWh/L. This is as good as regular gasoline (12.7 kWh/kg, 8.8 kWh/L) and diesel ((11.7 kWh/kg, 9.7 kWh/L) and significantly higher than ethanol (7.7 kWh/kg, 6.1 kWh/L) . This high energy density of EMF, the fact that these HMF derivatives can now be obtained in high yields, in one step, from very cheap hexose or hexose-containing starting materials such as sucrose and glucose, and as these ethers are, in contrast to HMF, liquids at room temperature, make these very interesting fuels or fuel additives. In certain embodiments, the alcohol is selected from the group consisting of primary (un) branched aliphatic alcohols. In certain preferred embodiments, the alcohol is selected from the group consisting of primary C1-C5 (un) branched aliphatic alcohols, preferably methanol, ethanol, 1-propanol, 2-hydroxymethyl-propanol, 1-butanol. More preferable are methanol and/or ethanol. The resulting (m) ethyl ether ( (m) ethoxymethy1furfural, MMF or EMF) has a high energy content and may directly be used as a fuel additive as an alternative for MTBE or as a fuel. Mixtures of alcohols may also be employed. Ethanol is the most preferred alcohol in the method of the present invention as the ethanol that is used can also be derived from biomass or glucose-containing material (bio-ethanol) .
The acid catalyst in the method of the present invention can be selected from amongst (halogenated) organic acids, inorganic acids, salts, Lewis acids, ion exchange resins and zeolites or combinations and/or mixtures thereof . In certain preferred embodiments, the acid catalyst is a heterogeneous catalyst. In certain embodiments, the acid catalyst is a homogenous catalyst. The acid may be a protonic, Brønsted or, alternatively, a Lewis acid. In certain embodiment, the acid may be organic or inorganic. In certain embodiments, the organic acid can be selected from amongst oxalic acid, levulinic acid, maleic acid or para-toluenesulphonic acid. In certain embodiments, the inorganic acid can be selected from amongst phosphoric acid, sulphuric acid, hydrochloric acid, hydrobromic acid, nitric acid, hydroiodic acid, optionally generated in situ. In certain embodiments, the inorganic acid is selected form the group of sulphuric acid, phosphoric acid, hydrochloric acid, nitric acid. In certain embodiments, the salt can be one of (NH4) 2SO4/SO3 , ammonium phosphate, triethylamine phosphate, pyridinium salts, pyridinium phosphate, pyridinium hydrochloride/hydrobromide/perbromate, DMAP, aluminium salts, Th and Zr ions, zirconium phosphate, Cr-, Al-, Ti-, Ca-, In-ions, ZrOC12, VO(SO4)2, TiO2 , V-porphyrine, Zr-, Cr-, Ti- porphyrine . In certain embodiments, the Lewis acid can be one of ZnCL2 , A1C13, BF3. In certain embodiments, the ion exchange resins can be one of Amberlite, Diaion, levatit. In certain embodiments, it is preferred that the acid catalyst is a solid catalyst that may be selected form the group consisting of acid resins, natural clay- mineral, zeolites, supported acids such as silica impregnated with mineral acids, heat treated charcoal, metal oxides, metal sulfides, metal salts and mixed oxides and mixtures thereof. In certain embodiments, mixtures or combinations of acid catalysts can be used.
The temperature at which the reaction is performed may vary, but in general it is preferred that the reaction is carried out at a temperature from 50 to 300 degrees Celsius, preferably from 125 to 250, more preferably from 175 to 225 degrees Celsius. In general, temperatures higher than 300 are less preferred as the selectivity of the reaction as many by-products occur, inter alia caramelisation of the sugar. Performing the reaction below the lowest temperature is also less preferable because of the slow reaction speed.
The fructose and/or glucose-containing starting material can be selected from a wide variety of feeds. In general any feed with a sufficient high fructose or glucose content can be used. It is preferred that the fructose and/or glucose -containing starting material is selected from the group of starch, amylose, galactose, cellulose, hemi-cellulose, glucose-containing disaccharides such as sucrose, maltose, cellobiose, lactose, preferably glucose-containing disaccharides, more preferably sucrose or glucose.
The catalyst can be added to the reaction mixture in an amount varying from 0.01 to 40 mole % drawn on the fructose or glucose content of the fructose and/or glucose -containing starting material preferably from 0.1 to 30 mole %, more preferably from 1 to 20 mole %.
In certain embodiments, one or more solvents or diluents may be added, in general to aid the dissolution of the glucose containing material or as a diluent. The solvent may be selected form the group consisting of water, sulfoxides, preferably DMSO, ketones, preferably methyl ethylketone, methylisobutylketone and acetone or mixtures of two or more of the above solvents .
In certain embodiments, the ratio of alcohol/solvent is from 50 to 0.1, preferably from 20 to 1, more preferably from 10 to 2. Higher amounts of alcohol may have the result that the reaction is too slow due to the limited solubility (hence availability of the starting material) , whereas too much solvent in the system may lead to a too high dilution, which in both cases are less preferred results. One of the possible solvents is water. In certain embodiments, the method can be performed in a continuous flow process. In such method, homogenous catalysts may be used and the residence time of the reactants in the flow process is between 0.1 second and 10 hours, preferably from 1 second to 5 hours, more preferably from 1 minute to 1 hour.
In certain embodiments the continuous flow process is a fixed bed continuous flow process or a reactive (catalytic) distillation process with preferably a heterogeneous acid catalyst. To initiate or regenerate the heterogeneous acid catalyst or to improve performance, an inorganic or organic acid may be added to the feed of the fixed bed or reactive distillation continuous flow process. In a fixed bed process, the liquid hourly space velocity (LHSV) can be from 1 to 1000, preferably from 5 to 500, more preferably from 10 to 250 and most preferably from 25 to 100.
As explained above, the application of the products of the method of the present invention, i.e. the ethers, is in the use as a fuel or fuel additive and as precursor for the manufacture of 2,5- di (hydroxymethyl) furan, furan-2, 5-dicarboxylic acid, 2- hydroxymethylfuran-5-carboxylic acid, 2,5-
(dihydroxymethyl) tetrahydrofuran, which can be used as monomers in a polymerisation process, optionally after conversion of the diol to a diamine. See for a review Moreau, Topics in catalysis, 2004, 27, 11-
30.
Figures: Figure 1. Plot of a) conversion, b) selectivity to furan derivatives versus space velocity. 180C, heterogeneous catalysts, reaction medium water. Catalyst 1:D; Catalyst 2: ■ Catalyst 3: * Catalyst 4: #. Figure 2. Plot of a) conversion, b) selectivity to furan derivatives versus space velocity. 180C, heterogeneous catalysts, reaction medium 88.7% ethanol. Catalyst 1:D; Catalyst 2: ■ Catalyst 3: * Catalyst 4:
Examples
Example 1 : In a continuous flow reactor, sucrose 10 mmol/1, dissolved in water/ethanol/10% H2SO4, was reacted at a temperature of 195 degrees Celsius with a residence time between 6 and 60 seconds and a flow rate of 10 ml/min, i.e. 3.33 ml/min/reactor . At 6 seconds, mainly conversion into fructose and glucose was observed, but at prolonged residence times, 2 main furan peaks were observed in the UV spectrum. Mass spectrometry identified these products as HMF and EMF with a selectivity of >90 % at a conversion of 25%.
Example 2 : In a continuous flow reactor, glucose 10 mmol/1, dissolved in water/ethanol/10% H2SO4, was reacted at a temperature of 195 degrees Celsius with a residence time between 6 and 60 seconds and a flow rate of 10 ml/min, i.e. 3.33 ml/min/reactor . At 30 seconds, 2 main furan peaks were observed in the UV spectrum. Mass spectrometry identified these products as HMF and EMF with a selectivity of >90 % at a conversion of 10%.
Apparatus
Continuous parallel flow reactor system consisting of four quartz reactors inserted in a silver heating block; temperature and flow regulators and three HPLC pumps. Two of the pumps deliver the liquid to the reactors and third one is employed to dilute the reaction products prior to collection.
Analytical Method
The reaction products were quantified with the aid of HPLC-analysis with an internal standard (saccharine, Sigma Aldrich) . A Merck- Hitachi L7000 chromatograph, equipped UV and RI detectors, was used.
Stationary phase were reverse phase C18 (Sunfire 3.5 μm, 4.6xl00mm, Waters) and cation exchange (SupelcogelH, 4.6x300mm, SigmaAldrich) columns connected in series. A gradient elution at a constant flow 0.6 ml/min and temperature 60 0C was used according to the following scheme.
Figure imgf000007_0001
General Procedure
A 1.25 wt% solution of glucose (99.7 % Sigma Aldrich) in water or 88.7 % ethanol was flowed through a fixed bed (200 μl) of a heterogeneous catalyst at 180 0C. Flow rates were chosen such to achieve a space velocity 0.25 or 0.5 min"1, i.e. contact time 2 or 4 tnin. Liquid coming out of the reactors was diluted by a mixture of water and ethanol (50:50) to prevent tubing blockages.
Catalysts tested: Catalyst 1 Zeolite beta SAR25 (CBV Zeolyst)
Catalyst 2 Zeolite Y high SAR (CBV Zeolyst)
Catalyst 5 Mordenite H SAR 90 (CBV Zeolyst)
Catalyst 7 Zeolite Y SAR 5.17 (CBV Zeolyst)
Contact time and space velocity were calculated as follows:
Sv= Frfeβd / Vcat
Sv space velocity (min"1) Frfeed flow rate feed (ml/min) / Vcat catalyst volume (ml)
tc =1/ Sv tc contact time (min)
Conversion of substrate, selectivity and yield of furan derivatives were calculated according to the following formulae:
X=IOO*!!^ substrate /m0 substrate
X conversion ( % )
TOr substrate amount of reacted substrate (mg) m0 substrate amount of substrate in feed (mg)
Scompound =100 *nr substrate / Ωθ substrate
Scompound selectivity to compound ( % ) nr substrate moles of substrate reacted n0 substrate moles of substrate in feed
Yield =100*nproduct /n0 substrate Yield yield ( % ) riproduct moles of product formed Catalysts tested:
Catalyst 1 Zeolite beta SAR25 (CBV Zeolyst)
Catalyst 2 Zeolite Y high SAR (CBV Zeolyst)
Catalyst 3 Mordenite H SAR 90 (CBV Zeolyst) Catalyst 4 Zeolite Y SAR 5.17 (CBV Zeolyst)
Reactions in water.
Figure 1 a) and b) show that a conversion achieved for the catalysts tested was 76% (Zeolite beta) . This catalyst gave 7% selectivity to HMF and EMF.
Zeolite Y with high SAR presented 9% selectivity to furans at 20% conversion. Y zeolite with low SAR (catalyst 4) shows selectivity of 4% at very low conversion. Mordenite presented both reduced activity and selectivity to furan derivatives. HMF was a main furan found in the reaction mixture.
Reactions in ethanol .
With the use of Zeolite beta about 4 % selectivity to HMF and EMF was achieved at 17% conversion at a low space velocity. For the other catalysts tested, the conversion developed initially to more than 20% and the selectivity was in the range between 1 and 3 %.
The predominant furan derivative was the desired EMF.
Figure imgf000009_0001
Figure imgf000009_0002
DATA Glucose + Ethanol with solid acid catalyst 1 glucose cone 55.5 mmol/L; 90% EtOH
Figure imgf000009_0003
ATA Sucrose + Ethanol with solid acid catalyst 1
Figure imgf000010_0001
Figure imgf000010_0002
engine test
In a small-scale model diesel engine, comparative testing is performed with normal commercial diesel as a fuel and the same commercial diesel to which samples of 1 wt.%, 2 wt.%, 3 wt.%, 5 wt%, and 10 wt.% HMF or EMF are added, respectively. The diesel samples with HMF are less homogenous on visual inspection (solid particles remain visible, flocculation) and above 5 wt.% HMF, a solid deposit is sometimes observed. EMF is added as a liquid and does not yield any mixing or flocculation problems. The engine is run stationary with a set volume (100 mL) of fuel until empty. HMF containing fuels run less regular, whereas EMF containing fuels run at a regular pace and for a longer period (up to 15%) . On visual inspection of the engine, EMF provides less visual contamination.

Claims

Claims
1. Method for the manufacture of ethers of 5-hydroxymethy1furfural by reacting a fructose and/or glucose-containing starting material with an alcohol in the presence of a catalytic or sub- stoechiometric amount of a heterogeneous acid catalyst.
2. Method according to claim 1, wherein the alcohol is selected from the group consisting of primary (un) branched aliphatic alcohols, preferably C1-C5 primary (un) branched aliphatic alcohols, more preferably methanol, ethanol, 1-propanol, iso- propanol , 1-butanol, most preferably methanol, ethanol, more particular preferable ethanol or mixtures thereof.
3. Method according to claim 1 or 2, wherein the acid catalyst is selected from the group consisting of solid (halogenated) organic acids, inorganic acids, salts, Lewis acids, ion exchange resins, zeolites or mixtures and/or combinations thereof .
4. Method according to claim 1, wherein the acid is a solid Brønsted acid.
5. Method according to claim 1, wherein the acid is a solid Lewis acid.
6. Method according to any one of the claims 1 to 5, wherein the reaction is performed at a temperature from 50 to 300 degrees Celsius, preferably from 125 to 250, more preferably from 175 to 225 degrees Celsius.
7. Method according to any one of the claims 1 to 6, wherein the fructose and/or glucose-containing starting material is selected from the group of starch, amylose, galactose, cellulose, hemi-cellulose, glucose-containing disaccharides such as sucrose, maltose, cellobiose, lactose, preferably glucose-containing disaccharides, more preferably sucrose or glucose .
8. Method according to any one of the claims 1 to 7 wherein one or more solvents or diluents are present in addition to the alcohol .
5 9. Method according to claim 8, wherein the solvent or solvents are selected form the group consisting of water, sulfoxides, preferably DMSO, ketones, preferably methyl ethylketone, methylisobutylketone and/or acetone and mixtures thereof.
10 10. Method according to claim 9, wherein the ratio of alcohol/solvent is from 50 to 0.1, preferably from 20 to 1, more preferably from 10 to 2.
11. Method according to any one of the claims 1 to 10, wherein the 15 method is performed in a continuous flow process.
12. Method according to claim 11, wherein the residence time in the flow process is between 0.1 second and 10 hours, preferably from 1 second to 5 hours, more preferably from 1 minute to 1
20 hour .
13. Method according to claim 12 , wherein the continuous flow process is a fixed bed continuous flow process.
5 14. Method according to claim 13, wherein the fixed bed comprises a heterogeneous acid catalyst.
15. Method according to claim 13, wherein the continuous flow process is a reactive distillation or a catalytic distillation 0 process.
16. Method according to claim 15, wherein in addition to a heterogeneous acid catalyst, an inorganic or organic acid catalyst is added to the feed of the fixed bed or catalytic 5 distillation continuous flow process.
17. Method according to claim 13-16, wherein the LHSV is from 1 to 1000, preferably from 5 to 500, more preferably from 10 to 250 and most preferably from 25 to 100. 0
8. Use of 5-alkoxymethylfurfural, preferably 5-methoxy- methylfurfural or 5 -ethoxy-methylfurfural as a fuel or as a fuel additive.
PCT/EP2007/002145 2006-03-10 2007-03-12 Method for the synthesis of 5-alkoxymethyl furfural ethers and their use WO2007104514A2 (en)

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