WO2010151343A1 - Catalytic conversion of cellulose to liquid hydrocarbon fuels by progressive removal of oxygen to facilitate separation processes and achieve high selectivities - Google Patents
Catalytic conversion of cellulose to liquid hydrocarbon fuels by progressive removal of oxygen to facilitate separation processes and achieve high selectivities Download PDFInfo
- Publication number
- WO2010151343A1 WO2010151343A1 PCT/US2010/023836 US2010023836W WO2010151343A1 WO 2010151343 A1 WO2010151343 A1 WO 2010151343A1 US 2010023836 W US2010023836 W US 2010023836W WO 2010151343 A1 WO2010151343 A1 WO 2010151343A1
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- WIPO (PCT)
- Prior art keywords
- acid
- valerolactone
- gvl
- yield
- catalyst
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Classifications
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- C07D309/08—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C10G—CRACKING 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
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- C10G3/00—Production of liquid hydrocarbon mixtures from oxygen-containing organic materials, e.g. fatty oils, fatty acids
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- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
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- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
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- C01B2203/0205—Processes for making hydrogen or synthesis gas containing a reforming step
- C01B2203/0227—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
- C01B2203/0233—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
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- C01B2203/12—Feeding the process for making hydrogen or synthesis gas
- C01B2203/1205—Composition of the feed
- C01B2203/1211—Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/12—Silica and alumina
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- C07C2527/054—Sulfuric acid or other acids with the formula H2Sn03n+1
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- C07C2527/167—Phosphates or other compounds comprising the anion (PnO3n+1)(n+2)-
- C07C2527/173—Phosphoric acid or other acids with the formula Hn+2PnO3n+1
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- C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- C07C2531/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
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- C10G2300/1014—Biomass of vegetal origin
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Definitions
- a difficulty in implementing this strategy is that chemical components used to deconstruct solid cellulose (e.g., sulfuric acid) may alter the performance of heterogeneous catalysts used subsequently to convert the soluble biomass-derived reactants to the desired fuels and/or chemicals. As a result, costly purification steps are required to implement a cascade catalytic process.
- the present invention is a cascading method to convert cellulose to liquid fuels that addresses this long-felt and unmet need.
- a first version of the invention is directed to a method for converting cellulose to pentanoic acid.
- the first version of the method comprises deconstructing biomass comprising cellulose to yield a product mixture comprising levulinic acid and formic acid.
- the levulinic acid is then converted to ⁇ -valerolactone (GVL).
- the ⁇ -valerolactone is then converted to pentanoic acid (PAA).
- the biomass-derived cellulose is deconstructed by reacting it with an acid, preferably an acid selected from the group consisting of sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, oxalic acid, acetic acid, acetic anhydride, and combinations thereof, and most preferably sulfuric acid.
- an acid preferably an acid selected from the group consisting of sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, oxalic acid, acetic acid, acetic anhydride, and combinations thereof, and most preferably sulfuric acid.
- Converting the levulinic acid to ⁇ -valerolactone may be accomplished by contacting the levulinic acid with a heterogeneous catalyst comprising a metal selected from the group consisting of Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, Pt, Ag, Au, and combinations thereof. It is preferred that the levulinic acid is converted to ⁇ -valerolactone by contacting the levulinic acid with a heterogeneous catalyst comprising Ru/C.
- Converting the ⁇ -valerolactone to pentanoic acid is preferably accomplished by contacting the ⁇ - valerolactone with a catalyst comprising a metal selected from the group consisting of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, W, Pd, Ag, Pt, Au, and combinations thereof, in the presence of hydrogen.
- a catalyst comprising a metal selected from the group consisting of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, W, Pd, Ag, Pt, Au, and combinations thereof, in the presence of hydrogen.
- the preferred catalyst for converting the ⁇ -valerolactone to pentanoic acid is a catalyst comprising a combination of Nb and Pd.
- the ⁇ -valerolactone formed in the inventive process is separated from the acidic reaction medium by extracting it into a polar, aprotic solvent, such as ethyl acetate, methyl acetate, acetone, dimethyl ether, diethyl ether, acetonitrile, tetrahydrofuran, and the like (either neat or in a solvent system comprising one or more polar, aprotic solvents).
- a polar, aprotic solvent such as ethyl acetate, methyl acetate, acetone, dimethyl ether, diethyl ether, acetonitrile, tetrahydrofuran, and the like (either neat or in a solvent system comprising one or more polar, aprotic solvents).
- a polar, aprotic solvent such as ethyl acetate, methyl acetate, acetone, dimethyl ether, diethyl ether, acetonit
- the pentanoic acid formed as described herein is decarboxylated to yield a product mixture comprising n-butenes, including 1-butene, a valuable alpha-olefin feedstock.
- 1-butene (CAS No. 106-98-9) is a high-volume monomer, with production exceeding 1 million pounds per year in the US (data from the American Chemical Society). It is easily polymerized using Ziegler-Natta catalysts, to yield poly(butylene).
- Another version of the present method is directed to method for converting cellulose to liquid fuels.
- the method comprises the steps noted earlier, namely: deconstructing biomass comprising cellulose to yield a product mixture comprising levulinic acid and formic acid; converting the levulinic acid to ⁇ -valerolactone; and converting the ⁇ -valerolactone to pentanoic acid.
- the pentanoic acid is then ketonized to yield 5-nonanone.
- the 5-nonanone so formed is useful in its own right as a solvent and fuel additive.
- the 5-nonanone can also be further manipulated to yield a host of valuable solvents, fuels, and fuel additives.
- the 5- nonanone can be hydrodeoxygenated to yield nonane.
- the 5-nonanone can be reduced to yield 5-nonanol.
- the 5-nonanol so formed can be dehydrated to yield nonene.
- the nonene can be dimerized to yield a mixture of C 9 and Cj 8 olefins.
- the mixture of C 9 and Ci 8 olefins can be hydrogenated to yield a mixture of alkanes.
- the nonene formed as described above can be isomerized to yield a mixture of branched olefins. If this version is used, hydrogenating the mixture of branched olefins yields a mixture of branched alkanes.
- the glucose reactant may be derived from any source, without limitation, but is preferably derived from biomass (i.e., plant material, vegetation, agricultural waste, as well as cellulose-containing consumer, commercial, and industrial waste).
- the method comprises hydrolyzing glucose derived from any source in an aqueous, acid-catalyzed reaction to yield a product mixture comprising levulinic acid and formic acid, and then converting at least a portion of the formic acid present in the product mixture to H 2 and CO 2 without separating the levulinic acid and formic acid present in the product mixture. At least a portion of the levulinic acid present in the product mixture is reduced to ⁇ -valerolactone using the H 2 produced from the formic acid.
- the glucose may be hydrolyzed by reacting it with an acid, such as (by way of example and not limitation) sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, oxalic acid, acetic acid, acetic anhydride, and combinations thereof.
- an acid such as (by way of example and not limitation) sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, oxalic acid, acetic acid, acetic anhydride, and combinations thereof.
- Converting the formic acid present in the product mixture to H 2 and CO 2 can be accomplished by contacting the product mixture with a heterogeneous catalyst comprising a metal selected from the group consisting of Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, Pt, Ag, Au, and combinations thereof.
- a catalyst comprising ruthenium on a support is preferred.
- the ⁇ -valerolactone so formed may be concentrated by extracting it into a solvent comprising a polar, aprotic solvent; or by evaporating the ⁇ -valerolactone so formed.
- the ⁇ -valerolactone may then be converted to any number of valuable products, including pentanoic acid and n-butenes. Converting the ⁇ -valerolactone to pentanoic acid can be accomplished by contacting the ⁇ -valerolactone with a catalyst comprising a metal selected from the group consisting of Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, W, Pd, Ag, Pt, Au, and combinations thereof, in the presence of hydrogen. A catalyst comprising Nb and Pd is preferred.
- At least a portion of the ⁇ -valero lactone can be decarboxylated by contacting it with a solid acid catalyst, to yield a product mixture comprising 1-butene.
- the ⁇ -valerolactone can also be decarboxylated by reacting it with a mineral acid selected from the group consisting of sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, acetic acid, acetic anhydride, oxalic acid, and combinations thereof.
- Decarboxylating the ⁇ -valerolactone can also be accomplished by reacting it with a heterogeneous catalyst comprising a metal selected from the group consisting of Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, Pt, Ag, Au, Ru and combinations thereof. All percentages, parts and ratios used herein are by weight of the total composition, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore, do not include solvents or byproducts that may be included in commercially available materials, unless otherwise specified.
- the catalysts described herein may be used without a support or disposed on an inert or catalytically active support. Any catalyst support now known or developed in the future, without limitation, may be used. Suitable supports include carbon in any form (including nano-particles, "buckyballs," single and multi-wall nanotubes, etc.), silica, titania, alumina, silica/alumina, zirconia, etc., in any form (e.g., spheres, tablets, Raschig rings, and the like), zeolites, etc.
- Solid acid catalysts may be used in the present method, including any ceramic acid or acidic molecular sieve such as an acidic zeolite, an aluminosilicate, a titanosilicate, a borosilicate, any mixed oxide such as tungstated zirconia, any phosphated or sulphated catalyst such as sulphated or phosphated metal oxide, or a phosphate or sulphuric acid catalyst such as niobium phosphate, any heteropoly acid and any acidic ion exchange resin, as well as any combination or subset of these supported on inert materials such as carbon.
- any ceramic acid or acidic molecular sieve such as an acidic zeolite, an aluminosilicate, a titanosilicate, a borosilicate, any mixed oxide such as tungstated zirconia, any phosphated or sulphated catalyst such as sulphated or phosphated metal oxide, or a phosphate or s
- homogeneous catalysts When homogeneous catalysts are used, it is preferred that residual homogenous catalyst from any earlier step in the method is present in a concentration of between 0 and about 2 M, more preferably between 0 and about 0.5 M, and more preferably still between 0 and about 0.1 M.
- the various reactions may be conducted under a host of temperature, pressure, and WHSV ranges. While not being limited to these ranges, it is preferred that the various reactions described herein be conducted at a temperature range of from about 300 K to about 1100 K, more preferably from about 350 K to about 800 K, and more preferably still from about 400 K to about 600 K. Reaction temperatures above and below these stated ranges are explicitly within the scope of the method claimed herein.
- the reactions are preferably conducted at pressures ranging from about 0.1 bar to about 300 bar, more preferably from about 1 bar to about 20 bar, and most preferably from about 1 bar to about 5 bar. Reaction pressures above and below these stated ranges are explicitly within the scope of the method claimed herein.
- the reactions are preferably conducted at a WHSV of from about 0.1 to about 50 h -1 , more preferably from about 0.1 to about 30 h -1 , and most preferably from about 0.1 to about 1O h -1 . WHSVs above and below these stated ranges are explicitly within the scope of the method claimed herein. Numerical ranges as used herein are intended to include every number and subset of numbers contained within that range, whether specifically disclosed or not.
- the methods of the present invention can comprise, consist of, or consist essentially of the essential elements and limitations of the method described herein, as well as any additional or optional ingredients, components, or limitations described herein or otherwise useful in synthetic organic chemistry.
- FIG. 1 depicts a strategy according to the subject method for converting solid cellulose to chemical intermediates (e.g., pentanoic acid, 5-nonanone, etc.) and/or producing liquid alkane fuels from functional intermediates.
- Solid cellulose (dotted outline) undergoes acid-catalyzed (H+) deconstruction in an aqueous solution of sulfuric acid (light grey), followed by conversion over a metal catalyst (Me) to ⁇ -valerolactone (GVL) and further conversion over a bi-functional catalyst containing metal and acid sites (Me/H+) to pentanoic acid, which separates spontaneously to form an organic liquid (dark grey).
- Pentanoic acid can undergo ketonization over a metal oxide catalyst (MeOx) to form 5-nonanone, the latter of which can be converted to liquid fuels (dashed outline).
- 5-nonanone can be converted to nonane over a bi-functional catalyst containing metal and acid sites (Me/H+).
- 5-nonanone can be converted to nonanol over a metal catalyst (Me), followed by dehydration to nonene combined with isomerization and/or oligomerization over an acid catalyst (H+), and completed by hydrogenation over a metal catalyst (Me).
- Chemicals and solvents (dashed-dotted outline) can also be produced from cellulose by using 5-nonanone and 5-nonanol, and/or by converting pentanoic acid to 1-butene by decarboxylation.
- FIG. 2A depicts a cascade approach for converting cellulose to GVL and using ethyl acetate (EtAc) to extract GVL from the aqueous solution of sulfuric acid (H 2 SO 4 ).
- EtAc ethyl acetate
- LA Levulinic acid
- FIG. 2B depicts a cascade approach for converting GVL obtained from cellulose (as depicted in FIG. 2A) to pentanoic acid (PA), then 5-nonanone, and subsequently to nonane or nonanol, taking advantage of the spontaneous separation of nonane and nonanol from water.
- the liquid stream of nonane can be used in jet and Diesel fuels.
- the liquid stream of nonanol can be converted by dehydration to C 9 olefins (for use in gasoline) or to a mixture Of C 9 and C 18 olefins (for use in jet and Diesel fuels) by dehydration combined with dimerization.
- FIGS. 3A, 3B, 3C, and 3D are pie charts depicting % carbon composition (carbon %) of the organic layer obtained after various reactions according to the present method.
- the component numbering corresponds to C 4 -C 5 alkanes (1), pentanal/pentanol (2), esters (3), 5-nonanone (4), C 6 -C 7 ketones (5), GVL (6) and pentanoic acid (7).
- FIG. 4 is a flowchart depicting integration of levulinic processing with gasification or pyrolysis to produce fuels and chemicals from biomass.
- the primary cellulose conversion sequence is shown in dark grey; hemi-cellulose conversion is shown in light grey; gas-formation processes are shown in white with a solid outline; chemical intermediates are shown in white with a dashed outline; energy and fuel production are shown in white with a dotted outline.
- FIG. 5 is a graph depicting levulinic acid percent yield per cycle ( ⁇ ) and cumulative (•) for the deconstruction of cellulose in 0.5 M sulfuric acid at 423 K.
- FIG. 6 is a graph depicting the conversion of levulinic acid (•), formic acid ( ⁇ ), and GVL percent yield (o) over 5 wt% Ru/C at 423 K.
- FIG. 7 is a graph depicting simulated results for vaporization of 79% GVL in sulfuric acid to determine the sulfuric acid % vaporization ( ⁇ ; •) and the required vaporization temperature (G ; o) for a H 2 to GVL ratio of 2. Red symbols correspond to results from Matlab software, and blue symbols correspond to results using AspenTech simulation software.
- FIG. 8 is a graph depicting simulated results for the vaporization of 79% GVL in sulfuric acid using AspenTech simulation software to determine the sulfuric acid % vaporization (•) and required vaporization temperature (o) for a H 2 -to-GVL ratio of 2:1 and also the sulfuric acid % vaporization (A) and vaporization temperature ( ⁇ ) for a H 2 - to-GVL ratio of 10:1.
- FIG. 9 is a schematic diagram of a vapor-phase flow reactor used for converting GVL to pentanoic acid as described herein.
- FIG. 11 is a graph depicting the ratio of outlet pentenoic acid (PEA) to GVL at increasing WHSV on SiAl. Solid lines present model fit as described in the Examples.
- FIG. 12 is a graph depicting the rate of production of CO 2 at increasing WHSV on SiAl.
- the thick solid line corresponds to the inlet flow of GVL ( ⁇ mol min -1 g cat -1 ). Solid lines present model fit as described in the Examples.
- FIG. 13 is a graph depicting the rate of production of PAA and CO 2 over a physical mixture of 10-to-l SiAl to Pd/C in excess H 2 . Solid lines present model fit as described in the Examples.
- FIG. 14 is a graph depicting the ratio of outlet PEA to GVL at increasing WHSV on Nb. Solid lines present model fit as described in the Examples.
- FIG. 15 is a graph depicting the rate of production of CO 2 at increasing WHSV on Nb. Solid lines present model fit as described in the Examples.
- FIG. 16 is a graph depicting the rate of production of PAA and CO 2 over physical mixture of 7 to 1 Nb to Pd/C in excess H 2 . Solid lines present model fit as described in the Examples.
- FIG. 17 is an energy diagram for producing of PAA, butene, CO 2 and PEA from GVL.
- FIG. 18 is a graph depicting an Arrhenius plot for production of PAA (r 4 ) and CO 2 (r 3 ) on SiAl and Nb.
- FIG. 19 is a graph depicting calculated change in ⁇ G Obs versus temperature.
- FIG. 20 is a graph depicting the dehydration and isomerization of 5-nonanol to n- nonene ( ⁇ ), Croctene a (o), C 2 -heptene a (A), C 3 -hexene a ( ⁇ ), cracking products' 3 (•) and aromatics 0 (t>)
- b. refers to alkenes with less than 9 carbon atoms;
- c. refers to trimethyl benzene, ethyl/methyl benzene.
- the present method is a cascading catalytic process for converting glucose derived from any source (but preferably from biomass-derived cellulose) to pentanoic acid and subsequently to 5-nonanone and other downstream products.
- 5-Nonanone is a C ⁇ ketone that serves as a precursor for producing gasoline, jet and Diesel fuels by catalytic upgrading strategies, e.g., reactions involving hydrogenation, dehydration, isomerization, and oligomerization steps.
- an acid catalyst for example, sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, acetic acid, acetic anhydride, etc.
- an acid catalyst for example, sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, boric acid, hydrofluoric acid, hydrobromic acid, acetic acid, acetic anhydride, etc.
- the glucose is then dehydrated in an acid-catalyzed reaction to yield levulinic acid and formic acid.
- a heterogeneous catalyst preferably Ru/C is then used to convert formic acid to H 2 and CO 2 .
- the H 2 so formed is used to reduce levulinic acid to GVL.
- the GVL product is both more hydrophobic than levulinic acid and boils at a lower temperature. This permits selective separation of the GVL from the aqueous mineral acid reaction solution. Most of the acid can be recycled back to the cellulose deconstruction reactor.
- An aqueous solution of GVL containing smaller amounts of acid is then passed over another catalyst (preferably Pd/niobia) in the presence of H 2 to yield pentanoic acid. This takes place via a combination of ring-opening and hydrogenation reactions over catalytic sites associated with niobia and Pd, respectively.
- the pentanoic acid so formed can subsequently be converted to 5-nonanone by ketonization over a suitable catalyst, preferably ceria/zirconia.
- a suitable catalyst preferably ceria/zirconia.
- a key advantage of the subject method is that the hydrophobic pentanoic acid and 5-nonanone products spontaneously separate from water, thus greatly simplifying the purification of the desired products produced from cellulose.
- the liquid stream of 5-nonanone can be used for chemical applications, or it can be processed further to produce a variety of transportation fuel components.
- 5-nonanone can undergo hydrodeoxygenation over a bi- functional catalyst containing metal and acid sites (R.
- pentanoic acid can undergo catalytic decarboxylation to 1-butene (J. Miller (1993), see Examples), providing a strategy for using cellulose to produce ⁇ -olefins for the polymer industry.
- An important aspect in converting cellulose to pentanoic acid and 5-nonanone is managing the mineral acid (preferably sulfuric acid) used in the cellulose deconstruction step.
- the preferred catalyst (Ru/C) used to convert levulinic acid and formic acid to GVL and CO 2 operates effectively in the presence of sulfuric acid.
- the sulfuric acid itself is not consumed during this catalytic step.
- the preferred palladium-based catalyst used to convert GVL to pentanoic also operates in the presence of sulfuric acid.
- the palladium-based catalyst reduces sulfuric acid to H 2 S. Therefore, it is desirable, but not required, to remove a significant fraction of the sulfuric acid from the aqueous solution after converting levulinic acid to GLV, and prior to converting the GVL to pentanoic acid. This minimizes the amount of H 2 S that must be removed from the H 2 gas stream (e.g., by scrubbing). At the same time, most of the sulfuric acid can be recycled back to the cellulose deconstruction reactor.
- the aqueous solution containing sulfuric acid (and small amounts of GVL) is then recycled back to the cellulose deconstruction reactor.
- the GVL in the recycled acid stream is inert during subsequent rounds of cellulose deconstruction.
- the organic fraction containing GLV undergoes further catalytic processing following removal of the ethyl acetate solvent in an evaporator.
- the heat required to vaporize the ethyl acetate solvent amounts to only 14% of the heat required to vaporize an equal mass of water. This is a result of the higher molecular weight and lower heat of vaporization for ethyl acetate.
- the aqueous solution of GVL and sulfuric acid is fed along with gaseous H 2 (at a H 2 :GVL molar ratio of from about 2:1 to about 10:1) to a vapor-liquid separator operating at a targeted temperature and pressure to produce a gas stream consisting primarily of water and GVL, with small amounts of sulfuric acid, and a liquid stream consisting primarily of sulfuric acid and small amounts of GVL.
- This separator takes advantage of the higher boiling point of sulfuric acid compared to GVL and water.
- a gas-liquid separator operating at 14 bar and a temperature near 473 K leads to a gas stream containing H 2 , water and 80% of the GLV, with only about 15% of the sulfuric acid (see the Examples and FIGS. 7 and 8).
- This gas stream may then optionally undergo further catalytic processing, and the liquid stream containing the remainder of the GVL and 85% of the sulfuric acid is recycled back to the cellulose deconstruction reactor.
- converting levulinic acid to GVL is beneficial in view of the lower boiling point of GVL compared to levulinic acid, leading to more effective separation from sulfuric acid, which boils at a higher temperature.
- FIGS. 2 A and 2B illustrate the cascading nature of the present method for converting solid cellulose to various products, such as nonane, nonanol, Cg olefins, or a mixture of C 9 and Ci 8 olefins.
- the effluent stream from one reactor is simply utilized as an inlet stream to a subsequent reactor without the need for an intervening complex separation step. The only separation required is a spontaneous separation of the effluent stream into multiple phases. The appropriate phase is then passed onto the next reaction in the cascade.
- This cascading approach for converting cellulose involves a limited number of processing steps, thereby minimizing capital costs of the process, while achieving high yields of C 9 -products.
- the present method will be employed at regional facilities to convert cellulose to C 9 - products.
- transportation costs are minimized.
- Biomass is a low density product; shipping it vast distances prior to processing is not economically efficient.
- the C 9 liquid product stream contains more that 90% of the energy content of the cellulose feedstock, but less than 35% of the mass of the cellulose feedstock.
- C 9 liquid product could be economically shipped to more centrally located facilities for subsequent processing to the final fuel and/or chemical products.
- FIG. 2A shows a first version of a method that uses the extraction strategy outlined above (employing ethyl acetate, EtAc, as a solvent) to separate and recycle sulfuric acid from GVL.
- an aqueous solution of sulfuric acid e.g., 0.5 M
- a carbon-supported ruthenium catalyst at 448 K is then employed to convert the formic acid in this solution to CO 2 and H 2 .
- the H 2 so formed reduces levulinic acid to GVL, a conversion that requires one mole of H 2 per mole of levulinic acid (see the Examples and FIG.
- H 2 released by the decomposition of formic acid is utilized in the catalytic reduction of levulinic acid.
- an optional H 2 recycle stream is shown in FIG. 2A (including CO 2 removal).
- the H 2 recycle loop ensures a constant presence of H 2 within the catalytic reaction chamber.
- the aqueous solution of GVL containing sulfuric acid is then contacted with ethyl acetate, leading to extraction of most of the GVL into the organic phase (yellow), and retention of the most of the sulfuric in the aqueous phase.
- the aqueous phase is then recycled back to the cellulose deconstruction reactor.
- the organic stream containing GVL and small amounts of sulfuric acid is sent to an evaporator, from which the ethyl acetate solvent is condensed and recycled back to the separator for further extraction of GVL.
- the liquid GVL stream from the evaporator is then sent with H 2 to a Pd/niobia catalyst operating at 548 K, over which the GVL is further reduced to pentanoic acid, followed by conversion over ceria/zirconia at 698 K to produce 5- nonanone by ketonization.
- water may be added to the GVL reactant stream to eliminate formation of carbonaceous deposits on the Pd/niobia catalyst.
- Table 1 summarizes results (carbon distribution and carbon selectivities) for the catalytic conversion of aqueous solutions of GVL (30-40 wt%) with different acid concentrations (0.02 to 0.04 M) over Pd(5%)/Nb 2 O 5 . (More extensive results are presented in the
- the main byproducts formed are butane (produced by decarboxylation of pentanoic acid, with stoichiometric amounts of CO x ), pentanal/1- pentanol/pentane (produced by successive hydrogenations of pentanoic acid), and the ester pentyl pentanoate (produced by esterification between pentanoic acid and 1 - pentanol).
- the organic layer produced is rich in pentanoic acid, with minor amounts of pentanal/1-pentanol, traces of pentyl pentanoate, unreacted GVL, and small amounts of butane and pentane dissolved in the oil as a consequence of the pressure of the system (see FIGS.
- FIG. 2B illustrates another version of the present method for direct production of 5- nonanone from aqueous acid solutions of GVL by using a second bed of ceria-zirconia in a cascade mode.
- a 40 wt% GVL aqueous solution with a sulfuric acid concentration of 0.02 M can be efficiently converted to an organic stream (accounting for almost 90% of the carbon fed) that is rich in 5-nonanone over a Pd(5%)/Nb 2 O 5 + Ce 0.5 Zro 5 O 2 double bed arrangement (see FIG. 3C), with good stability versus time-on-stream (See also the Examples and FIG. 10).
- 5-Nonanone is produced along with stoichiometric amounts of CO 2 .
- the C 9 ketone is generated with almost 90% selectivity (Table 1).
- the main by-products of the process are 2-hexanone and 3-heptanone, produced by scission of 5-nonanone at the alpha and beta positions, respectively. These by-products also accumulate in the organic layer (see FIG. 3C). Importantly, their presence would not affect the subsequent processes of the cascade approach depicted in FIG. 2B because they form olefins in the gasoline range.
- 2-Hexanone and 3-heptanone can also be oligomerized to produce C 12 - C 14 alkanes that fall within the jet and Diesel fuel ranges.
- the preferred ceria-zirconia bed was operated at a higher temperature (698 K) than Pd(5%)/Nb 2 O 5 (548 K) to achieve complete conversion of the pentanoic acid formed in the first bed (see Table 3, entries 7 and 8).
- This stream of 5-nonanone can be converted at 523 K to nonane for use in jet and
- metal e.g., Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, Pt, Ag, Au, and combinations thereof
- acid sites e.g., silica-alumina, etc.
- the water may then be recycled back to the GVL stream entering the reactor containing the Pd/niobia catalyst.
- the liquid stream of linear nonene undergoes isomerization over a zeolite catalyst (e.g., ZSM-5 at 523 K) to produce branched C 9 -OIeHnS (or alkanes upon subsequent hydrogenation) for use as gasoline components.
- a zeolite catalyst e.g., ZSM-5 at 523 K
- nonene undergoes dimerization over an acid catalyst (e.g., "AMBERL YST"-brand catalysts at 433 K) to produce a mixture of C 9 and C 18 olefins (or alkanes upon subsequent hydrogenation) for use in jet and Diesel fuels.
- AMBERLYST is a registered trademark of Rohm & Haas Company, a wholly owned subsidiary of Dow Chemical Company.
- the present method achieved elevated levels of levulinic acid in water (e.g. , 20 wt%) at 423 K by adding solid cellulose to the aqueous solution of sulfuric acid (0.5 M) in the reactor at various stages of the deconstruction step.
- the levulinic acid yield is above 60% for the first cycle and gradually decreases with each cycle of cellulose addition, such that the final overall levulinic acid yield is equal to 52% after 5 cycles (see the Examples and FIG. 5).
- This approach avoids having high levels of cellulose in the slurry at any given time, thereby achieving effective mixing in the reactor over the entire period of deconstruction.
- This approach also avoids having high concentrations of glucose in the reactor at any given time, thereby minimizing undesirable polymerization reactions that lead to humins and which decrease the yield to levulinic acid (Girisuta (2007)).
- this strategy is effective because the levulinic acid and formic acid products are stable and inert at the reaction conditions used for cellulose deconstruction.
- the products formed during the deconstruction of a given batch of cellulose do not degrade during subsequent rounds of deconstruction. Nor do the products formed interfere with or inhibit subsequent rounds of deconstruction.
- the conversion of cellulose to levulinic acid using the present method was roughly 52-60%. This yield can be increased to approximately 60-65% by optimizing the reaction conditions (Girisuta (2007)).
- the cellulose that is not converted to levulinic acid can be burned to supply combined heat and power at locations near to the biomass growth area.
- this solid fraction can be utilized to provide heat (by combustion) and H 2 (by gasification) required for the processing of the levulinic fraction to liquid hydrocarbon fuels (Koppatz).
- the following stoichiometric equation represents the conversion of glucose to nonane, CO 2 and H 2 O:
- Synergies may be achieved by coupling biomass gasification with the present process for converting cellulose to pentanoic acid, 5-nonanone, and/or liquid hydrocarbons.
- the present method produces high- value, chemical intermediates and/or liquid hydrocarbons with high selectivity from the cellulose fraction of biomass, it does not convert all of the carbon present in biomass.
- biomass gasification can be employed on all components present in biomass. Because biomass-gasification processes can be carried out at atmospheric pressure, converting aqueous solutions of GVL into pentanoic acid and/or 5-nonanone at atmospheric pressure was explored.
- this biomass fraction comprising mainly xylose units, is converted primarily to furfural during the biomass deconstruction step.
- the furfural may be vaporized and thereby removed from the aqueous solution for other applications, as implemented in the Biofine process (S. W. Fitzpatrick. Patent 1990).
- the solid biomass feedstock can be subjected to an aqueous pretreatment step in which the hemi-cellulose fraction is hydrolyzed to produce xylose (Kumar (2009)).
- aqueous solution is then used to produce H 2 by aqueous-phase reforming (Cortright (2002)), thereby providing H 2 for converting GVL to chemicals and/or fuels as described herein.
- xylose can be converted to mono-functional intermediates (e.g. ,
- xylose can be selectively converted by dehydration to furfural (Chheda (2007)), which can then be used in chemical applications or can be converted to liquid fuels, such as methyltetrahydrofuran or liquid alkanes by aldol-condensation combined with hydrodeoxygenation reactions (Huber (2007), West (2008)).
- FIG. 4 is a schematic representation of a scenario for integrating levulinic acid processing with gasification to balance hydrogen production and utilization during the production of fuels and chemicals from biomass.
- the hemi-cellulose fraction of biomass is used to produce H 2 and CO 2 .
- this fraction is converted to furfural or mono-functional intermediates as precursors to fuels and chemicals.
- the cellulose fraction is used to produce GVL.
- Gasification is used to produce H 2 , CO 2 , CO and CH 4 from the lignin fraction and the solid humins formed during cellulose processing.
- the GVL intermediate is then converted to pentanoic acid using H 2 produced from xylose or gasification.
- the liquid stream of pentanoic acid can be converted to high value chemicals, such as 1-butene or 5-nonanone.
- the 5-nonanone can be upgraded further to liquid hydrocarbon fuels using H 2 produced from xylose or via gasification (see Examples).
- the remainder of the high heating value gas produced from xylose or gasification can be used for combined heat and power production.
- FIG. 4 also shows how biomass processing is accomplished by integrating levulinic acid processing with pyrolysis.
- the H 2 required for levulinic acid processing is provided by the hemi-cellulose fraction of biomass.
- Pyrolysis is then employed to process the lignin fraction of biomass as well as solid humins produced from converting cellulose to levulinic acid.
- the pyrolysis processing can be carried out to produce bio-oil, or it can be carried out with the addition of a catalyst to produce aromatic fuels (Huber).
- the liquid products from the cellulose deconstruction step, the conversion of levulinic acid into GVL, and the GVL extraction step were analyzed by HPLC (Waters 2695 system with a Bio-Rad Aminex HPX-87H column and a RI 410 detector) (Waters Corp., Milford, MA, USA; Bio-Rad Laboratories, Hercules, CA, USA).
- the liquid products from the conversion of GVL into pentanoic acid and the conversion of pentanoic acid into nonanone were analyzed by GC-MS (Shimadzu GC-2010 with a mass spectrometer and DB-5ms column from Alltech) and GC (Shimadzu GC-2010 with a FID detector and Rtx-5 column from Alltech) (Shimadzu Corporation, Kyoto, Japan; Alltech Associates, Inc., Deerfield, IL, USA).
- Product identification was verified using a combination of GC-MS for volatile species, and retention times for GC and HPLC. The products were purchased and calibrated for GC and HPLC.
- Shimadzu GC-8A (equipped with TCD detector and an Alltech packed column model HayeSep DB 100/120) was used to detect CO, CO 2 and H 2 S.
- a Varian GC (Saturn 3) (Varian, Inc., Palo Alto, CA, USA) using a FID detector and a GS-Q capillary column (Agilent Technologies, Santa Clara, CA, USA) was used to detect other volatile organic compounds.
- the overall carbon balance gave recoveries ranging from 93-111%, and the sulfur balance closed to 73-111%.
- Pd(5%)/Nb 2 O 5 was prepared by incipient wetness impregnation of a commercial niobium oxide (HY-340 from Companhia Brasileira de Metalurgia e Mineracao
- Microcrystalline cellulose (8 g, 5% moisture) with an average size of 20 ⁇ m and a 0.5 M sulfuric acid solution (92 g) were loaded into a 450 mL Parr Instruments alloy C- 276 batch reactor equipped with a variable speed mechanical stir and Teflon liner (Parr Instrument Co., Moline, IL, USA).
- the reactor was pressurized with inert gas (35 bar) and heated to 423 K (1.4 K min -1 ) with a 590 W electric heating mantle.
- the reactor was maintained at 423 K for 6 h while stirring. At the end of the reaction time the heating mantle was removed and the reactor was cooled with compressed air.
- a liquid sample 400 ⁇ L was collected, syringe filtered (0.2 ⁇ m membrane), and analyzed by HPLC. After a cycle of cellulose deconstruction, another batch of microcrystalline cellulose (8 g, 5% moisture) was added to the reaction mixture and the vessel was resealed. The same procedure as above was performed for multiple cycles. The solid remaining at the end of the reaction was separated from the solution via vacuum filtration and an elemental analysis for C, H, and S was performed (Galbraith Labs, Knoxville, TN, USA). The elemental analysis results indicated that the remaining solid composition was 67.32 wt% carbon, 4.83 wt% hydrogen and 0.06 wt% sulfur.
- the results of five cellulose deconstruction cycles are shown in FIG. 5.
- the levulinic acid yield is above 60% for the first cycle and gradually decreased with each recycle.
- the final overall levulinic acid yield is about 52%.
- the number of moles of formic acid produced was equal to the number of moles of levulinic acid formed (within about 5%).
- the levulinic acid and formic acid solution resulting from the 5-cycle cellulose deconstruction experiment discussed above was reacted over a 5 wt% Ru/C catalyst (1.02 g, Sigma Aldrich).
- the catalyst and a sample of the prepared solution (40 g, 15 wt% levulinic acid, 7.5 wt% formic acid) was loaded into a 450 mL Parr Instruments alloy C- 276 batch reactor equipped with a variable speed mechanical stir and Teflon liner.
- the reactor was purged with inert gas and then pressurized with hydrogen (35 bar) at ambient temperature.
- the reactor was heated to 423 K (1.4 K min -1 ) and then held constant for 4 h.
- Ethyl acetate (96%, Sigma Aldrich) was used to extract GVL from the solution prepared by the deoxygenation of levulinic acid discussed above.
- a sample (5.001 g, 1.068 g/mL) of the GVL solution was mixed with ethyl acetate (4.996 g) in a sealed glass container and shaken vigorously for 1 min. The solution was allowed to settle and the ethyl acetate layer was removed with a transfer pipette (5.309 g). The remaining aqueous layer (4.736 g, 1.062 g/mL) was analyzed by HPLC. It was determined that 76% of the GVL was extracted into the ethyl acetate as well as 3% of the H 2 SO 4 and 6% of the water.
- the amount of water extracted into the ethyl acetate layer increased with increasing GVL extraction, while the sulfuric acid extraction increased only for the highest GVL concentration tested.
- the effect of sulfuric acid concentration on the extraction of GVL and water was minimal for a 20 wt% GVL solution.
- the evaporative separation of GVL from sulfuric acid was modeled in Matlab software (The Mathworks, Natick, MA, USA) by solving vapor-liquid equilibrium relations and also using AspenTech chemical simulation software (Aspen Technology, Inc., Burlington, MA, USA).
- a 20 wt% GVL solution containing 0.1 M sulfuric acid was used as the feed into a separation unit.
- a flash drum operating at a specified temperature and pressure was modeled for both simulation methods. Each model assumed that the solution entered the flash drum at the temperature and pressure of the flash drum. For all calculations, the operating pressure was set at a desired value and held constant while the temperature required to vaporize 79% of the GVL was determined. Hydrogen, as an inert sweep gas, was introduced to determine the effect of sparging.
- FIG. 9 A schematic diagram of the flow reaction system used for the reaction kinetics studies is shown in FIG. 9.
- a 1/4" tubular reactor made of corrosion resistant commercial hastelloy C-276 alloy was used for these studies of feed solutions containing H 2 SO 4 .
- the catalyst (3.5 g of Pd(5%)/Nb 2 ⁇ 5) was fixed in the tubular reactor between two end-plugs of carbon wool.
- a 1/4" tubular stainless steel reactor was loaded first with Pd(5%)/Nb 2 ⁇ 5 (3.0 g), followed by ceria-zirconia (5.0 g). Both beds were separated by a carbon wool plug.
- the reactor was mounted in an upflow configuration and surrounded by aluminum blocks heated externally by a well-insulated furnace (Applied Test Systems Inc.).
- thermocouple (Omega) was attached to the outside of the reactor to measure temperature, which was controlled with a 1600 series type temperature controller (Dwyer Instruments, Michigan City, IN, USA ). Prior to reaction kinetics studies, fresh catalyst was reduced in flowing H 2 (100 cm 3 (STP) min -1 ). The catalyst was heated, using a linear temperature ramp (1 K min '1 ) to the final reduction temperature (538 K) and held at this temperature for 3 h, and then heated to the reaction temperature under flowing H 2 . The flow- rate ofH 2 was fixed with a Brooks Model 5850 mass-flow controller (Brooks Instrument, Hatfield, PA, USA).
- the system pressure was controlled by a backpressure regulator (GO Regulator, Model BP-60) (GO Regulator, Spartanburg, SC, USA).
- GO Regulator GO Regulator, Spartanburg, SC, USA.
- a liquid solution containing varying amounts (30-40 wt%) of GVL (Sigma- Aldrich) and sulfuric acid (0.02- 0.04 M) in deionized water was introduced into the upflow reactor using an HPLC pump
- FIG. 10 shows a plot of the yield of 5-nonanone versus time-on-stream for the conversion of GVL over a double-bed consisting of Pd(5%)/Nb 2 O 5 followed by Ce 0 5 Zr 0 5 O 2 .
- Amorphous silica-alumina MCC 25, Grace Davison (Columbia, MD, USA) with a Si/Al ratio of 4
- niobic acid HY-340, CBMM
- Pd/C 1% Sigma Aldrich
- Insulated aluminum blocks were heated using a K-type thermocouple ("DiGi-Sense”- brand, Eutech Instruments Pte Ltd., Singapore) between the blocks and reactors to monitor the temperature, which was controlled by a series 16A temperature controller (Love Controls, a division of Dwyer Instruments, Inc., Michigan City, IN, USA).
- the H 2 flow rate was controlled with a 5850E Brooks Instruments mass flow controller while the liquid feed was controlled with a Lab Alliance Series 1 HPLC pump.
- the liquid effluents were drained from the separator and analyzed by GC (Shimadzu GC-2010, FID, SHRX5 column) and by GC- MS (Shimadzu GC-2010 SHRX1-5MS column).
- thermodynamics of the ring opening of GVL to pentenoic acid isomers (PEA) followed by subsequent hydrogenation or decarboxylation were studied in an upflow reactor at atmospheric pressure and temperatures from 498 K to 623 K.
- the reactive scheme is shown in Scheme 1.
- GVL is reacted via acid-catalyzed ring opening to form 4, 3-cis and 3-trans pentenoic acid. These species can further isomerize on acid sites to form 2-cis and 2-trans pentenoic acid or can revert back to GVL.
- the isomers of PEA can react in the absence of metal catalyst to form either butene and CO 2 . In the presence of a metal catalyst, the PEA isomers rapidly form pentanoic acid (PAA).
- silica alumina SiAl
- the feed for all runs comprised a 10 wt% GVL solution in water.
- the weight hourly space velocity (WHSV) defined as the mass of GVL per mass of catalyst per hour, was adjusted by changing either the inlet flow of feed solution, or by changing the mass of solid acid catalyst.
- a continuous hydrogen sweep was adjusted to keep the partial pressure of all species in the reactor constant for all temperatures and all values of WHSV at 0.016, 0.164, and 0.820 (bar) for GVL, H 2 and water, respectively.
- the hydrogen flow was chosen such that the molar ratio of H 2 -to-GVL of 10: 1.
- FIG. 11 The relative outlet concentration of PEA-to-GVL at temperatures of 523 to 623 K and varying WHSV are shown in FIG. 11. As the temperature increased, the ratio also increased, from an average value of 0.13 at 523 K to 0.88 at 623 K. Not included in FIG. 11 are the data points collected at 498 K and those at 623 K and low space velocity. At 498 K the low concentration of PEA was near the limit of detection for quantification. At low WHSV and 623 K, the rate of decarboxylation was greater than 80% making these points unrepresentative of the actual ratio.
- FIG. 12 shows the observed production of CO 2 over the same temperatures and WHSV values as in FIG. 11.
- the average rate of CO 2 production was 0.07 umol min -1 g cat -1 while at 623 K and high WHSV where the rate was not limited by the inlet flow rate of species, the rate of CO 2 production was 95 umol min -1 g cat -1 .
- a temperature of 623 K and a space velocity of about 0.1 to 1 h -1 (g GVL g cat -1 h -1 )
- Table 4 Production of Butene and CO 2 from GVL over Silica Alumina The conversion in Table 4 was calculated from the unreacted GVL observed in the liquid effluent. The yield to mixed butene isomers was calculated from the observed gas phase effluents. In addition to butene, small amounts of the products methane, ethane, ethene, propane, propene, and pentane, were observed in the gas phase. The results in Table 4 were performed over the same catalytic bed. The run without sulfuric acid was performed first, followed by the sulfuric acid run.
- This reactive scheme as a means of producing butene from biomass is novel and inventive.
- the expected low cost of levulinic acid, and associated low cost of catalyst makes this process an economical way of producing a highly reactive and useful compound from biomass without supplying hydrogen to the reaction.
- the rate of ring opening was also measured in the absence of solid acid as a function of temperature on a system loaded with 0.1 g of Pd/C and crushed silica and operating at a flow rate of 0.04 mL min -1 .
- This flow rate corresponds to a typical WHSV (as defined for the solid acid catalyst) of 0.1 - 0.5 hr -1 .
- the rate of ring opening and rate of decarboxylation were approximately 3% of the comparable acid-catalyzed rates at 523 K and dropped off to less than 0.2% at 623 K, thus indicating that crushed silica and Pd/C do not contribute significantly to the ring opening of GVL.
- FIG. 14 shows the relative outlet concentration of PEA to GVL at temperatures of 548 to 598 K and varying WHSV.
- an increase in temperature increases the ratio of PEA to GVL from an average value of 0.16 at 548 K to 0.52 at 598 K.
- the observed production of CO 2 over the same temperatures and WHSV values as FIG. 14 is shown in FIG. 15.
- the average rate of CO 2 production spans from 0.48 to 38 ⁇ mol min -1 g cat " 1 from 548 to 598 K.
- the 4-position ester was formed in 25-30% yield, while the 3-cis and 3-trans were formed in 65-75% yield with the 2-cis and 2-trans making up the remaining 1-5%.
- the directly formed isomers are removed before isomerization, while in the current investigation, they are not and can thus isomerize to the 2- cis and 2-trans isomers.
- the isomers of PEA can react in the absence of metal catalyst to form butene and CO 2 . However, in the presence of a metal catalyst the isomers rapidly form PAA.
- the total energy diagram for this system can be represented as shown in FIG. 17.
- the system follows the solid line.
- the system follows the dashed line.
- the molecules involved in this study were simulated using Gaussian-brand software (Gaussian, Inc., Walingford, CT, USA). Starting from GVL, the formation of either butene and CO 2 or PAA, are calculated as favored at all temperatures with standard enthalpy of -22 kJ mol " and Gibbs energy change -77 kJ mol -1 at 298 K for GVL to CO 2 and butene.
- thermodynamics favors the formation of GVL over PEA isomers.
- Values for the ring opening of GVL to 4-pentenoic acid were calculated as having an enthalpy of reaction of 36 kJ mol -1 at 298 K which compares favorably with the reported literature value of 38-40 kJ mol -1 .
- the other isomers of pentenoic acid were calculated to have a lower enthalpy of reaction from GVL with 2-trans having the lowest value, 17 kJ mol " l , followed by 3-trans, 2-cis, and lastly 3-cis with values of 25, 26, 32 kJ mol -1 , respectively.
- the calculated change in Gibbs energy at 298 K for GVL to PEA isomers follows the same trend as the enthalpy with values of 25, 8, 14, 16, and 19 kJ mol -1 for 4, 2-trans, 3-trans, 2- cis, and 3-cis.
- the expected concentrations as a function of temperature can be calculated using the simulated thermodynamic values including the calculated heat capacity.
- the simulated change in enthalpy and entropy for GVL to all PEA isomers is 25 kJ mol -1 and 53 J mol -1 K -1 , respectively.
- the formation of PEA becomes more favorable than the formation of GVL. It is therefore expected, that as the temperature is increased, the relative ratio of PEA to GVL should also increase. When equilibrium is established, this ratio should remain constant. At higher flows, if the forward rate of ring opening is to slow relative to the inlet flow of reactant, this ratio should decrease.
- Ea 2 and Ea 3 can be calculated for each catalytic system from equations 10 and 11.
- Eai is 113 kJ mol -1 and E a3 Total is 149 kJ mol -1 .
- Ea 2 by difference is 58 kJ mol -1 while Ea 3 is 94 kJ mol -1 .
- Eai is 104 kJ mol -1
- E 33 10131 is 113 kJ mol -1 . Therefore, Ea 2 is 49 kJ mol -1 while Ea 3 is 58 kJ mol -1 .
- the model was next run using the simulated values for the enthalpy and entropy, 25 kJ mol -1 and 53 J mol -1 K -1 .
- the model was unable to converge on values for the activation energy and pre-exponential factors for rates 1 and 3 that gave good representation of the data.
- Nb is much more active in the ring opening of GVL on a per mass basis. See also Table 5.
- the measured acid site density of SiAl is 578 ⁇ mol g -1 while the B.E.T. surface area is 498m 2 g -1 .
- the values are 135 ⁇ mol g -1 and 118 m 2 g -1 . Therefore on a per acid site basis, Nb is much more active for the ring opening under the conditions of this study.
- 5-nonanol was dehydrated to produce an isomeric mixture of 1-, 2-, 3-, and 4-nonene over an H-ZSM-5 catalyst in a packed bed reactor operated in an upflow configuration (see FIG. 9).
- the catalyst (4.0 g) was loaded in a 1 A" stainless steel tubular reactor with the remaining volume filled by fused silica granules that had been ground to a uniform particle size.
- the catalyst bed was held in place by plugs of quartz wool at the reactor entrance and exit.
- the tubular reactor was mounted inside of an aluminum cylinder at the center of a well insulated furnace.
- a Type K thermocouple was affixed to the external wall of the reactor and the temperature was controlled by a 1600 Series feedback temperature controller (Dwyer Instruments).
- the ZSM-5 catalyst Prior to use, the ZSM-5 catalyst was activated by thermal calcinations as previously described and the temperature was ramped to 453 - 473 K for the dehydration reaction.
- the reactor was pressurized with H 2 (50 cm 3 (STP) min -1 ) to 35 bar and maintained using a back pressure regulator (GO Regulator, Model-BP-60).
- the 5-nonanol feed was introduced via an HPLC pump (Lab Alliance, Series 1) at a WHSV of 0.6 h -1 .
- the reactor effluent was collected in a gas-liquid separator (Jerguson Gage & Valve Co., Stafford, TX, USA) at room temperature and drained for GC analysis.
- the reaction results are summarized in Table 6.
- the conversion of nonene to C 18 alkanes was performed over an Amberlyst-70 catalyst in a packed bed reactor operating in a downflow configuration.
- the catalyst (4.0 g, dried) was loaded into a 1/4" tubular stainless steel reactor.
- the catalyst bed was held in place by plugs of quartz wool at the reactor entrance and exit.
- the tubular reactor was mounted inside of an aluminum cylinder at the center of a well insulated furnace.
- a Type K thermocouple was affixed to the external wall of the reactor and the temperature was controlled by a 1600 Series feedback temperature controller (Dwyer Instruments).
- the reactor was pressurized with He and maintained using a back pressure regulator (Tescom, Model 26-2322-26-043, Elk River, MN, USA).
- the dehydration and isomerization of 5-nonanol was performed over a US Y-zeolite catalyst (Engelhard/BASF, BASF AG, Ludwigshafen, Germany).
- the catalyst was loaded into a 1/4" tubular stainless steel reactor operating in an upflow configuration. Prior to reaction, the catalyst was calcined in situ under flowing air (25 cm 3 (STP) min -1 ) by ramping the temperature (1 h) to 773 K and holding for 2 h.
- the reactor was cooled to the reaction temperature and pure 5-nonanol (Sigma Aldrich) was introduced using an HPLC pump (Lab Alliance Series 1).
- the reactor effluent was collected at room temperature in a gas-liquid separator (Jerguson) and drained for GC analysis. Results for the 5-nonanol dehydration and isomerization at atmospheric pressure and a WHSV of 0.6 hr -1 at two temperatures (573 and 623 K) are shown in FIG. 20.
- GVL was converted to butene and CO 2 over an amorphous silica alumina catalyst.
- the catalyst was loaded into in a 1/4" tubular stainless steel reactor operating in an upflow configuration. The catalyst bed was held in place by plugs of quartz wool at the reactor entrance and exit.
- the tubular reactor was mounted inside of an aluminum cylinder at the center of a well insulated furnace (Applied Test Systems).
- a Type K thermocouple (Omega) was affixed to the external wall of the reactor and the temperature was controlled by a 1600 Series feedback temperature controller (Dwyer Instruments).
- a GVL solution was introduced into the reactor using an HPLC pump (Lab Alliance Series 1).
- the reactor effluent was collected at room temperature in a gas-liquid separator (Jerguson) and drained for GC analysis. The reactor pressure was maintained at atmospheric pressure for all experiments.
- a 30 wt% GVL feed was reacted with and without the addition of H 2 SO 4 (0.04 M) to the feed solution.
- the results for the 30 wt% GVL feed solutions are shown in Table 4, above.
- the conversion data in Table 4 were calculated from the unreacted GVL observed in the liquid effluent. High butene yields were observed for GVL feeds (10-30 wt%) with and without H 2 SO 4 .
- the yield to mixed butene isomers was calculated from the observed gas phase effluents. No deactivation was observed over the total reaction time (40 h).
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989010362A1 (en) | 1988-04-26 | 1989-11-02 | Biofine Incorporated | Lignocellulose degradation |
US5883266A (en) * | 1998-01-16 | 1999-03-16 | Battelle Memorial Institute | Hydrogenated 5-carbon compound and method of making |
US20060162239A1 (en) * | 2004-12-23 | 2006-07-27 | Van Den Brink Peter J | Process for the hydrogenation of a lactone or of a carboxylic acid or an ester having a gamma-carbonyl group |
EP1918247A1 (en) * | 2006-10-18 | 2008-05-07 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Hydrogen production from formic acid |
WO2008142127A1 (en) * | 2007-05-22 | 2008-11-27 | Shell Internationale Research Maatschappij B.V. | Process for converting levulinic acid into pentanoic acid |
WO2009007391A1 (en) * | 2007-07-12 | 2009-01-15 | Shell Internationale Research Maatschappij B.V. | Process for converting levulinic acid into pentanoic acid |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3065263A (en) * | 1959-11-17 | 1962-11-20 | Rayonier Inc | Process for the manufacture of levulinic acid |
US20070208183A1 (en) * | 2006-03-02 | 2007-09-06 | Haan Rene J | Hydrogenation process for the conversion of a carboxylic acid or an ester having a carbonyl group |
-
2009
- 2009-06-23 US US12/490,129 patent/US8148553B2/en active Active
-
2010
- 2010-02-11 EP EP10704693A patent/EP2445992A1/en not_active Withdrawn
- 2010-02-11 BR BRPI1011989A patent/BRPI1011989A2/en not_active Application Discontinuation
- 2010-02-11 WO PCT/US2010/023836 patent/WO2010151343A1/en active Application Filing
-
2012
- 2012-02-09 US US13/369,388 patent/US8624043B2/en active Active
-
2013
- 2013-12-02 US US14/093,907 patent/US9067903B2/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1989010362A1 (en) | 1988-04-26 | 1989-11-02 | Biofine Incorporated | Lignocellulose degradation |
US5883266A (en) * | 1998-01-16 | 1999-03-16 | Battelle Memorial Institute | Hydrogenated 5-carbon compound and method of making |
US20060162239A1 (en) * | 2004-12-23 | 2006-07-27 | Van Den Brink Peter J | Process for the hydrogenation of a lactone or of a carboxylic acid or an ester having a gamma-carbonyl group |
EP1918247A1 (en) * | 2006-10-18 | 2008-05-07 | Ecole Polytechnique Fédérale de Lausanne (EPFL) | Hydrogen production from formic acid |
WO2008142127A1 (en) * | 2007-05-22 | 2008-11-27 | Shell Internationale Research Maatschappij B.V. | Process for converting levulinic acid into pentanoic acid |
WO2009007391A1 (en) * | 2007-07-12 | 2009-01-15 | Shell Internationale Research Maatschappij B.V. | Process for converting levulinic acid into pentanoic acid |
Non-Patent Citations (21)
Title |
---|
A. S. MAMMAN; J. M. LEE; Y. C. KIM; I. T. HWANG; N. J. PARK; Y. K. HWANG; J. S. CHANG; J. S. HWANG, BIOFUELS BIOPRODUCTS & BIOREFINING, vol. 2, no. 5, 2008, pages 438 - 454 |
ARNO DE KLERK, IND. ENG. CHEM. RES., vol. 44, 2005, pages 3887 - 3893 |
B. GIRISUTA; L.P.B.M. JANSSEN; H.J. HEERES, IND. ENG. CHEM. RES., vol. 46, no. 6, 2007, pages 1696 - 1708 |
C. GAERTNER; J. C. SERRANO-RUIZ; D. J. BRADEN; J. A. DUMESIC, JOURNAL OF CATALYSIS, 2009 |
C. H. CHRISTENSEN; J. RASS-HANSEN; C. C. MARSDEN; E. TAAMING; K. EGEBLAD, CHEMSUSCHEM, vol. 1, 2008, pages 283 - 289 |
E.L. KUNKES; D.A. SIMONETTI; R.M. WEST; J.C. SERRANO-RUIZ; C.A. GAERTNER; J.A. DUMESIC, SCIENCE, vol. 322, no. 5900, 2008, pages 417 - 421 |
G. W. HUBER; A. CORMA, ANGEW. CHEM. INT. ED., vol. 46, 2007, pages 7184 - 7201 |
GAO Y ET AL: "The interconversion of formic acid and hydrogen/carbon dioxide using a binuclear ruthenium complex catalyst", JOURNAL OF THE CHEMICAL SOCIETY, DALTON TRANSACTIONS, CHEMICAL SOCIETY. LETCHWORTH, GB LNKD- DOI:10.1039/B004234J, 1 January 2000 (2000-01-01), pages 3212 - 3217, XP002426814, ISSN: 1472-7773 * |
HEERES HANS ET AL: "Combined dehydration /(transfer)-hydrogenation of C6- sugars (D- glucose and D-fructose) to .gamma.-valerolactone using ruthenium catalysts", GREEN CHEMISTRY, ROYAL SOCIETY OF CHEMISTRY, CAMBRIDGE, GB LNKD- DOI:10.1039/B904693C, vol. 11, no. 8, 4 June 2009 (2009-06-04), pages 1247 - 1255, XP009123484, ISSN: 1463-9262, [retrieved on 20090604] * |
HUBER GEORGE W ET AL: "Synthesis of transportation fuels from biomass: Chemistry, catalysts, and engineering", CHEMICAL REVIEWS, ACS,WASHINGTON, DC, US LNKD- DOI:10.1021/CR068360D, vol. 106, no. 9, 1 September 2006 (2006-09-01), pages 4044 - 4098, XP002490759, ISSN: 0009-2665, [retrieved on 20060627] * |
J. A. MILLER; J. A. NELSON; M. P. BYRNE, J. ORG. CHEM., vol. 58, 1993, pages 18 - 20 |
J. ABBOT; B. W. WOJCIECHOWSKI, J. CATAL., vol. 108, 1987, pages 346 - 355 |
J. CHHEDA; G. HUBER; J.A. DUMESIC, ANGEW. CHEM. INT. ED., vol. 46, no. 38, 2007, pages 7164 - 7183 |
J. ROBINSON, BIOMASS BIOENERGY, vol. 26, no. 5, 2004, pages 473 - 483 |
J.C. SERRANO-RUIZ; J. LUETTICH; A. SEPULVEDA-ESCRIBANO; F.J. RODRIGUEZ-REINOSO, J. CATAL., vol. 241, 2006, pages 45 |
M. RENZ, EUR J ORG CHEM, 2005, pages 979 - 988 |
P. KUMAR; D. M. BARRETT; M. J. DELWICHE; P. STROEVE, IND. ENG. CHEM. RES., vol. 48, 2009, pages 3713 - 3729 |
R. M. WEST; Z. Y. LIU; M. PETER; J. A. DUMESIC, CHEMSUSCHEM, vol. 1, 2008, pages 417 - 424 |
R.D. CORTRIGHT; R.R. DAVDA; J.A. DUMESIC, NATURE, vol. 418, no. 6901, 2002, pages 964 - 967 |
S. KOPPATZ; C. PFEIFER; R. RAUCH; H. HOFBAUER; T. MARQUARD-HOELLENSTEDT; M. SPECHT, FUEL PROC. TECH., 2009 |
S. ZHU, GREEN CHEM., vol. 8, 2006, pages 325 - 327 |
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Also Published As
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US20100324310A1 (en) | 2010-12-23 |
US8148553B2 (en) | 2012-04-03 |
BRPI1011989A2 (en) | 2018-02-20 |
US20140094618A1 (en) | 2014-04-03 |
US9067903B2 (en) | 2015-06-30 |
US20120149922A1 (en) | 2012-06-14 |
EP2445992A1 (en) | 2012-05-02 |
US8624043B2 (en) | 2014-01-07 |
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