Technical Field
[0001] The current invention concerns a process for preparing a fuel additive concentrate
from a renewable resource (biomass), and to the fuel additive concentrate comprising
a fuel and fuel additives which are made from a renewable resource.
Background Art
[0002] Fuel, fuel additives and various chemicals used in the petrochemical industry are
derived from oil, gas and coal, all finite sources. Biomass, on the other hand, is
considered a renewable source. Biomass is biological material (including biodegradable
wastes) which can be used for the production of fuels or for industrial production
of e.g. fibres, chemicals or heat. It excludes organic material which has been transformed
by geological processes into substances such as coal or petroleum.
[0003] Production of biomass derived products for non-food applications is a growing industry.
Bio-based fuels are an example of an application with strong growing interest.
[0004] Biomass contains sugars (hexoses and pentoses) that may be converted into value added
products. Current blofuel activities from sugars are mainiy directed towards the fermentation
of sucrose or glucose into ethanol or via complete breakdown via Syngas to synthetic
liquid fuels.
EP 0641 854 describes the use of fuel compositions comprising of hydrocarbons and/or vegetable
oii derivatives containing at least one giyceroi ether to reduce particulate matter
emissions.
[0005] More recently, the acid catalysed reaction of fructose has been re-visited, creating
HMF as an intermediate of great interest. Most processes investigated have the disadvantage
that HMF is not very stable at the reaction conditions required for its formation.
Fast removal from the water-phase containing the sugar starting material and the acid
catalyst has been viewed as a solution for this problem. Researchers at the University
of Wisconsin-Madison have developed a process to make HMF from fructose. HMF can be
converted into monomers for plastics, petroleum or fuel extenders, or even into fuel
itself. The process by prof. James Dumesic and co-workers first dehydrates the fructose
in an aqueous phase with the use of an acid catalyst (hydrochloric acid or an acidic
ion-exchange resin). Salt is added to salt-out the HMF into the extracting phase.
The extracting phase uses an inert organic solvent that favors extraction of HMF from
the aqueous phase. The two-phase process operates at high fructose concentrations
(10 to 50 wt %), achieves high yields (80% HMF selectivity at 90% fructose conversion),
and delivers HMF in a separation-friendly solvent (
DUMESIC, James A, et al. "Phase modifiers promote efficient production of Hydroxymethylfurfural
from fructose". Science. 30 juni 2006, vol.312, no.5782, p.1933-1937). Although the HMF yields from this process are interesting, the multi-solvent process
has cost-disadvantages due to the relatively complex plant design and because of the
less than ideal yields when cheaper and less reactive hexoses than fructose, such
as glucose or sucrose, are used as a starting material. HMF is a solid at room temperature
which has to be converted in subsequent steps to useful products. Dumesic has reported
an integrated hydrogenolysis process step to convert HMF into dimethylfuran (DMF),
which is assumed to be an interesting gasoline additive.
[0006] In
WO 2006/063220 a method is provided for converting fructose into 5- ethoxymethylfurfural (EMF) at
60 °C, using an acid catalyst either in batch during 24 hours or continuously via
column elution during 17 hours. Applications of EMF were not discussed.
[0007] Also in copending patent application
PCT/EP2007/002145 the manufacture of HMF ethers are described, including the use of such ethers as
fuel or fuel additive. Indeed, both the methyl ether and the ethyl ether (methoxymethylfurfural,
or MMF; ethoxyethylfurfural or EMF) were prepared and tested.
[0008] Indeed, there is a growing interest in the preparation of the so-called furanics,
wherein the expression furanics is used to include all derivatives of furan and tetrahydrofuran,
which are derived from biomass and are used as fuel additive.
[0009] These interesting fuel additives, however, still have to be isolated in a separate
process step from the polar solvent used, which thus increases the overall costs of
their production, before they can be used as fuel additive. The inventors have therefore
set out to overcome this shortfall.
[0010] Surprisingly, the inventors have found that the aforementioned furanics and in particular
the ethers of HMF and subsequent derivatives thereof may be effectively and efficiently
isolated from the solvents wherein they are produced using fuel as extractant. The
extraction provides a fuel additive which can be further concentrated, diluted or
added as such to the fuel.
Disclosure of Invention
[0011] Accordingly, the current invention provides a fuel additive concentrate and a method
for the manufacture of a fuel additive concentrate comprising a biomass-derived furan
derivative and/or tetrahydrofuran derivative dissolved in a fuel, by extracting said
derivative from the polar solvent wherein the derivative is produced, using a fuel
as extractant. The method is of particular interest in the extraction of ethers of
5-hydroxymethyl-2-furfural and/or further derivatives thereof.
[0012] The current invention also provides for the use of the fuel additive concentrate.
[0013] Fuels for extracting and forming the fuel component of the fuel additive concentrate
include but are not limited to gasoline and gasoline-ethanol blends, kerosene, diesel,
biodiesel (all renewable fuels combustible in a diesel engine), Fischer-Tropsch liquids
(for example obtained from GTL, CTL or BTL gas-to-liquids/coal-to-liquids/biomass
to liquids processes), diesel-biodiesel blends and green diesel and blends of diesel
and/or biodiesel with green diesel (green diesel is a hydrocarbon obtained by hydrotreating
biomass derived oils, fats, greases or pyrolysis oil; see for example the UOP report
OPPORTUNITIES FOR BIORENEWABLES IN OIL REFINERIES FINAL TECHNICAL REPORT, SUBMITTED
TO: U.S. DEPARTMENT OF ENERGY (DOE Award Number: DE-FG36-05GO15085)). Fuels for blending
with the product of the present invention may also include one or more other furanics,
wherein the expression furanics is used to include all derivatives of furan and tetrahydrofuran.
The invention also provides a fuel composition comprising a fuel element as described
above and the reaction product made according to the present invention.
Mode(s) for Carrying Out the Invention
[0014] Biomass resources are well known. The components of interest in biomass are the mono-,
di- or polysaccharides (hereinafter referred to as hexose-containing starting material).
Suitable 6-carbon monosaccharides include but are not limited to fructose, glucose,
galactose, mannose and their oxidized, reduced, etherified, esterified and amidated
derivatives, e.g. aldonic acid or alditol, with glucose being the most abundant, the
most economic and therefore the most preferred monosaccharide albeit less reactive
than fructose. On the other hand, the current inventors have also succeeded to convert
sucrose, which is also available in great abundance. Other disaccharides that may
be used include maltose, cellobiose and lactose. The polysaccharides that may be used
include cellulose, inulin (a polyfructan), starch (a polyglucan) and hemi-cellulose.
The polysaccharides and disaccharides are converted into their monosaccharide component(s)
and dehydrated during the manufacture of the 5-HMF ether.
[0015] The current inventors and various other researchers have succeeded in the conversion
of the hexose-containing starting material. By way of example hereafter is described
the preparation of 5-HMF ethers by reacting a hexose-containing starting material
with an alcohol in the presence of an acid catalyst. It should be noted, however,
that similar ethers may be made by conversion of the hexose-containing starting material
with an olefin in the presence of a suitable catalyst system.
[0016] Alcohols used in the manufacture of 5-HMF ethers are typically monoalcohols, having
a primary hydroxyl group. The alcohol may, however, be branched, containing some unsaturated
carbon-carbon double bonds, and bear more than one hydroxyl group. Also, rather advantageously
mixtures of alcohols may be used; the product which is used as fuel additive does
not need to be pure.
[0017] Preferred are alcohols having 4 carbon atoms or more, although methanol, ethanol
and (iso)propanol may be used as well.
[0018] The amount of alcohol used during the manufacture of the HMF ether is preferably
at least equimolar on the hexose content of the feedstock, but typically is used in
much greater excess. Indeed, the alcohol may be used as solvent or co-solvent. In
such a case, a sufficient amount of alcohol is present to form the HMF ether.
[0019] The acid catalyst used in the preparation of an HMF ether can be selected from amongst
(halogenated) organic acids, inorganic acids, Lewis acids, ion exchange resins and
zeolites or combinations and/or mixtures thereof. It may be a homogeneous catalyst,
but heterogeneous catalysts are preferred for purification reasons. The HMF ethers
can be produced with a protonic, Brønsted or, alternatively, a Lewis acid or with
catalysts that have more than one of these acidic functionalities.
[0020] The protonic acid may be organic or inorganic. For instance, the organic acid can
be selected from amongst oxalic acid, levulinic acid, maleic acid, trifluoro acetic
acid (triflic acid), methansulphonic acid or para-toluenesulphonic acid. Alternatively,
the inorganic acid can be selected from amongst (poly)phosphoric acid, sulphuric acid,
hydrochloric acid, hydrobromic acid, nitric acid, hydroiodic acid, optionally generated
in situ.
[0021] Certain salts may be used as catalyst, wherein the salt can be any one or more of
(NH
4)
2SO
4/SO
3, ammonium phosphate, pyridinium chloride, triethylamine phosphate, pyridinium salts,
pyridinium phosphate, pyridinium hydrochloride/hydrobromide/perbromate, DMAP, aluminium
salts, Th and Zr ions, zirconium phosphate, Sc and lanthanide ions such as Sm and
Y as their acetate or trifiuoroactate (triflate) salt, Cr-, Ai-, Ti-, Ca-, in-ions,
ZrOCl
2, VO(SO
4)
2, TiO
2, V-porphyrine, Zr-, Cr-, Ti-porphyrine.
[0022] Lewis acids selected as dehydration catalyst can be any one of ZnCl
2, AlCl
3, BF
3. ion exchange resins can be sultable dehydration catalysts. Examples include Amberlite™
and Amberlyst™, Diaion™ and Levatit™. Other solid catalyst that may be used include
natural clay minerals, 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.
[0024] The amount of catalyst may vary, depending on the selection of catalyst or catalyst
mixture. For instance, the catalyst can be added to the reaction mixture in an amount
varying from 0.01 to 40 mole % drawn on the hexose content of the biomass resource,
preferably from 0.1 to 30 mole %, more preferably from 1 to 20 mole %.
[0025] In the preferred embodiment, the catalyst is a heterogeneous catalyst.
[0026] 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 degrees Celsius, more preferably from 150 to 225
degrees Celsius. In general, temperatures higher than 300 are less preferred as the
selectivity of the reaction reduces and 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 low reaction rate.
[0027] The hexose-containing starting material is typically dissolved or suspended in a
solvent which can be the alcohol reactant, in order to facilitate the reaction. 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. Also so-called ionic liquids may be
used. The latter refers to a class of inert ionic compounds with a low melting point,
which may therefore be used as solvent. Examples thereof include e.g., 1-H-3-methyl
imidazolium chloride, discussed in "
Dehydration of fructose and sucrose into 5-hydroxymethylfurfural in the presence of
1-H-3-methyl imidazolium chloride acting both as solvent and catalyst", by Claude
Moreau et al, Journal of Molecular Catalysis A: Chemical 253 (2006) 165-169.
[0028] Basically a sufficient amount of solvent is preferably present to dissolve or to
suspend the starting material and to limit undesired side-reactions.
[0029] The method of the current invention may be carried out in a batch process or in a
continuous process, with or without recycle of (part of) the product stream to control
the reaction temperature (recycle via a heat exchanger). For instance, the method
of the invention 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, preferable from 1 second to 1 hours, more preferably
from 5 seconds to 20 minutes. Alternatively, the continuous flow process may be a
fixed bed continuous flow process or a reactive (catalytic) distillation process with
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 min
-1.
[0030] The above process results in a stable HMF ether, which may be converted into a further
derivative before being used as fuel and/or as fuel additive.
[0031] The characterizing feature of the current invention is that the fuel additives (plus
some additional combustible by-products) may be extracted by liquid-liquid extraction
using a fuel as extraction solvent. The extraction itself may be performed cross-currently
or countercurrently using conventional equipment (e.g., a series of mixers/settlers).
The fuel additive concentrate will therefore comprise a fuel component and a biomass-derived
furan derivative and/or tetrahydrofuran derivative dissolved in the fuel. The latter
component may be present in amounts ranging from a 1 vol% upwards, preferably 5 vol%
upwards to 80 vol% or less, preferably 50 vol% or less.
[0032] The polar phase (comprising the reaction solvent) may be -and preferably is- recycled
for use in subsequent conversion of hexose-containing starting material.
[0033] No extraordinary temperature or pressure conditions apply. Obviously, using a fuel
as extractant, the conditions should be selected such that none of the components
(fuel, the furanics, the reaction solvent or the preceding reactants, if any) evaporate.
[0034] Having isolated the fuel additives in the fuel, the fuel additive concentrate may
be further concentrated by removing (some) of the fuel. The concentrate may contain
conventional quantities of conventional additives such as cetane improvers, friction
modifiers, detergents, antioxidants and heat stabilizers, for example. Especially
preferred fuel additive concentrates are diesel fuel formulations that comprise diesel
fuel hydrocarbons and HMF ether as above described together with peroxidic or nitrate
cetane improvers such as ditertiary butyl peroxide, amyl nitrate and ethyl hexyl nitrate
for example.
References
[0035]
- DUMESIC, James A, et al. "Phase modifiers promote efficient production of Hydroxymethylfurfural
from fructose". Science. 30 June 2006, vol.312, no.5782, p.1933-1937.
- WO 2006/063220
- Chapter 15 of Advanced Organic Chemistry, by Jerry March, and in particular under
reaction 5-4. (3rd ed., © 1985 by John Wiley & Sons, pp. 684-685).
- LEWKOWSKI, Jaroslaw. Synthesis, chemistry and applications of 5-hydroxymethylfurfural
and its derivatives. Arkivoc. 2001, p.17-54.
- MOREAU, Claude, et al. "Dehydration of fructose and sucrose into 5-hydroxymethylfurfural
in the presence of 1-H-3-methyl imidazolium chloride acting both as solvent and catalyst",
Journal of Molecular Catalysis A: Chemical 253 (2006) p. 165-169.
- EP 0641 854
- UOP report OPPORTUNITIES FOR BIORENEWABLES IN OIL REFINERIES FINAL TECHNICAL REPORT,
SUBMITTED TO: U.S. DEPARTMENT OF ENERGY (DOE Award Number: DE-FG36-05GO15085)
- Adv. Synth. Catal. 2001, 343, 220-225
1. Method for the manufacture of a fuel additive concentrate comprising a biomass-derived
furan derivative and/or tetrahydrofuran derivative dissolved in a fuel, by extracting
said derivative from the polar solvent wherein the derivative is produced, using a
fuel as extractant.
2. Method according to claim 1, wherein the biomass-derived furan derivative and/or tetrahydrofuran
derivative is an ether of 5-hydroxymethyl-2-furfural and/or a further derivative thereof,
prepared by reacting a hexose-containing starting material with an alcohol in the
presence of an acid catalyst, or with an olefin in the presence of a catalyst system.
3. Fuel additive concentrate, obtainable by the method according to claim 1 or 2.
4. Fuel additive concentrate according to claim 3, comprising a fuel component and a
biomass-derived furan derivative and/or tetrahydrofuran derivative dissolved in the
fuel, wherein the biomass-derived derivative or derivatives is/are present in amounts
ranging from a 1 vol% upwards, preferably 5 vol% upwards to 80 vol% or less, preferably
50 vol% or less.
5. Fuel additive concentrate according to claim 3 or 4, comprising conventional quantities
of conventionai additives such as cetane improvers, friction modifiers, detergents,
antioxidants and heat stabilizers.
6. Fuei additive concentrate according to any one of the claims 3 to 5, comprising diesel
fuel hydrocarbons and an ether of 5-hydroxymethyl-2 furfural and/or a further derivative
thereof together with peroxidic or nitrate cetane improvers such as ditertiary butyl
peroxide, amyl nitrate and ethyl hexyl nitrate.
7. A fuel or fuel composition comprising the fuel additive concentration produced by
the method of any one of claims 1 or 2 or as defined in any one of claims 3-5, blended
with one or more of gasoline and gasoline-ethanol blends, kerosene, diesel, biodiesel,
Fischer-Tropsch liquids, diesel-biodiesel blends and green diesel and blends of diesel
and/or biodiesel with green diesel and other furanics.