WO2008069985A1 - Fabrication de butènes et de dérivés de ceux-ci à partir d'éthanol aqueux - Google Patents
Fabrication de butènes et de dérivés de ceux-ci à partir d'éthanol aqueux Download PDFInfo
- Publication number
- WO2008069985A1 WO2008069985A1 PCT/US2007/024669 US2007024669W WO2008069985A1 WO 2008069985 A1 WO2008069985 A1 WO 2008069985A1 US 2007024669 W US2007024669 W US 2007024669W WO 2008069985 A1 WO2008069985 A1 WO 2008069985A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- reaction product
- degrees
- mpa
- butene
- recovered
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/20—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms
- C07C1/24—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as heteroatoms by elimination of water
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
- C07C11/08—Alkenes with four carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/02—Monocyclic hydrocarbons
- C07C15/067—C8H10 hydrocarbons
- C07C15/08—Xylenes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/32—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
- C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
- C07C2521/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
- C07C2521/08—Silica
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
- C07C2523/16—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- C07C2523/24—Chromium, molybdenum or tungsten
- C07C2523/30—Tungsten
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/02—Sulfur, selenium or tellurium; Compounds thereof
- C07C2527/053—Sulfates or other compounds comprising the anion (SnO3n+1)2-
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- C07C2527/02—Sulfur, selenium or tellurium; Compounds thereof
- C07C2527/053—Sulfates or other compounds comprising the anion (SnO3n+1)2-
- C07C2527/054—Sulfuric acid or other acids with the formula H2Sn03n+1
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2529/00—Catalysts comprising molecular sieves
- C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
- C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
- C07C2529/18—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the mordenite type
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- 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
- C07C2531/06—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
- C07C2531/08—Ion-exchange resins
- C07C2531/10—Ion-exchange resins sulfonated
Definitions
- the present invention relates to the production of butenes and derivatives thereof from aqueous ethanol, optionally obtained from a fermentation broth.
- ethanol can be recovered from a number of sources, including synthetic and fermentation feedstocks. Synthetically, ethanol can be obtained by direct catalytic hydration of ethylene, indirect hydration of ethylene, conversion of synthesis gas, homologation of methanol, carbonylation of methanol and methyl acetate, and synthesis by both homogeneous and heterogeneous catalysis. Fermentation feedstocks can be fermentable carbohydrates (e.g., sugar cane, sugar beets, and fruit crops) and starch materials (e.g., grains including corn, cassava, and sorghum).
- fermentable carbohydrates e.g., sugar cane, sugar beets, and fruit crops
- starch materials e.g., grains including corn, cassava, and sorghum
- yeasts from the species including Saccharomyces can be employed, as can bacteria from the species Zymomonas, particularly Zymomonas mobilis.
- Ethanol is generally recovered as an azeotrope with water, so that it is present at 95.57 weight percent with respect to the weight of water and ethanol combined. See Kosaric, et. al, Ullmann's Encyclopedia of Industrial Chemistry, Sixth Edition, Volume 12, pages 398-473, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany, and P. L. Rogers, et al., Adv. Biochem. Eng. 23 (1982) 27-84.
- 1- butanol can be prepared by condensation from ethanol over basic catalysts at high temperature using the so-called "Guerbet Reaction.” See for example, J. Logsdon in Kirk-Othmer Encyclopedia of Chemical Technology, John Wiley and Sons, Inc., New York, 2001.
- Butenes are useful intermediates for the production of linear low density polyethylene (LLDPE) and high density polyethylene (HDPE), as well as for the production of transportation fuels and fuel additives.
- LLDPE linear low density polyethylene
- HDPE high density polyethylene
- the bulk of butenes (1-butene, 2-butene, isobutene) are currently produced as byproducts in the refining of motor fuel, and from the various cracking processes of butane, naphtha, or gas oil (Weissermel, K. and Arpe, H.-J. (translated by Lindley, CR. and Hawkins, S.) in Industrial Organic Chemistry, 4 th Edition (2003) pages 66-667, Wiley-VCH Verlag GmbH & Co. KgaA, Weinheim, Germany).
- Butenes can also be useful intermediates for the production of isooctanes and isooctenes, which can then be used as intermediates for the production of xylenes, particularly p-xylene.
- xylenes particularly p-xylene.
- the production of p-xylene is detailed in co-owned U.S. Pat. No. 7,067,708.
- a process for making at least one butene comprising: a) contacting a reactant comprising wet ethanol with a base catalyst to make a first reaction product comprising 1-butanol; b) recovering from the first reaction product a partially-purified first reaction product consisting essentially of 1-butanol and no more than 5 weight percent water based on the weight of the 1-butanol and water combined; c) contacting the partially-purified first reaction product of step (b), optionally in the presence of a solvent, with at least one acid catalyst at a temperature of about 50 degrees C to about 450 degrees C and a pressure from about 0.1 MPa to about 20.7 MPa to produce a second reaction product comprising at least one butene; and d) recovering said at least one butene from said second reaction product to obtain at least one recovered butene.
- the ethanol of step a) above is obtained from a fermentation broth.
- the butenes so produced can be used to produce derivatives such as isoalkanes, Cio to C 13 substituted aromatic compounds, butyl alkyl ethers, isooctenes, isooctanes, isooctanols, and isooctyl alkyl ethers.
- the isooctanes and isooctenes can be further converted to p-xylene.
- the p- xylene can be further converted to terephthalic acid, a component of polyesters.
- the present invention relates to a process for making butenes from aqueous ethanol via dry butanol.
- dry 1-butanol denotes a material that is predominantly 1-butanol, but may contain small amounts of water (under about 5% by weight relative to the weight of the 1-butanol plus the water), and may contain small amounts of other materials, such as acetone and ethanol, as long as they do not materially affect the catalytic reaction previously described when performed with reagent grade 1-butanol.
- the expression “consisting essentially of means herein that the 1-butanol may include small amounts of other components as long as they do not affect substantially the performance of combined 1-butanol and water in subsequent process steps.
- the aqueous ethanol can be obtained from any convenient source, including fermentation using microbiological processes known to those skilled in the art.
- the fermentative microorganism and the source of the substrate are not critical for the purposes of this invention.
- the result of the fermentation is a fermentation broth, which is then refined to produce a stream of aqueous ethanol.
- the refining process may comprise at least one distillation column to produce a first overhead stream that comprises ethanol and water. If the first distillation column is insufficient to produce a first overhead stream with a desired ethanol content, then the first overhead stream can be introduced into a second distillation column to produce a second overhead stream, and so on, ultimately leading to the aqueous ethanol (having at least 5% water) required as the reactant in the present invention.
- These streams, which are vaporous can be used directly in the current process, or can be condensed and revaporized for use at a later time.
- the stream of aqueous ethanol (which may be diluted with an inert gas such as nitrogen and carbon dioxide) is contacted with at least one base (or basic) catalyst in the vapor or liquid phase at a temperature of about 150 degrees C to about 500 degrees C and a pressure from about 0.1 MPa to about 20.7 MPa to produce a first reaction product comprising water and butanol.
- the first reaction product will also comprise unreacted ethanol, a variety of organic products, and water.
- the organic products include butanols, predominantly 1-butanol.
- the at least one base catalyst can be a homogeneous or heterogeneous catalyst.
- Homogeneous catalysis is catalysis in which all reactants and the catalyst are molecularly dispersed in one phase.
- Homogeneous base catalysts include, but are not limited to, alkali metal hydroxides.
- Heterogeneous catalysis refers to catalysis in which the catalyst constitutes a separate phase from the reactants and products. See, for example, Hattori, H. (Chem. Rev. (1995) 95:537-550) and Solid Acid and Base Catalysts (Tanabe, K., in Catalysis: Science and Technology, Anderson, J. and Boudart, M (eds.) 1981 Springer-Verlag, New York) for a description of solid catalysts and how to determine whether a particular catalyst is basic.
- a suitable base catalyst useful in the current process is either a substance which has the ability to accept protons as defined by Bronsted, or as a substance which has an unshared electron pair with which it can form a covalent bond with an atom, molecule or ion as defined by Lewis.
- suitable base catalysts may include, but may not be limited to, metal oxides, hydroxides, carbonates, silicates, phosphates, aluminates and combinations thereof.
- Preferred base catalysts may be metal oxides, carbonates, silicates, and phosphates.
- Preferred metals of the aforementioned compounds may be selected from Group 1 , Group 2, and rare earth elements of the Periodic Table. Particularly preferred metals may be cesium, rubidium, calcium, magnesium, lithium, barium, potassium and lanthanum.
- the base catalyst may be supported on a catalyst support, as is common in the art of catalysis.
- Suitable catalyst supports may include, but may not be limited to, alumina, titania, silica, zirconia, zeolites, carbon, clays, double-layered hydroxides, hydrotalcites and combinations thereof. Any method known in the art to prepare the supported catalyst can be used.
- One method for preparing supported catalysts is to dissolve a metal carboxylate salt in water.
- a support such as silica is wet with the solution, then calcined. This process converts the supported metal carboxylate to the metal oxide, carbonate, hydroxide or combination thereof.
- the support can be neutral, acidic or basic, as long as the surface of the catalyst/support combination is basic.
- the base catalysts of the present invention may further comprise catalyst additives and promoters that will enhance the efficiency of the catalyst.
- the relative percentage of the catalyst promoter may vary as desired. Promoters may be selected from the Group 8 metals of the Periodic Table, as well as copper and chromium.
- the base catalysts of the invention can be obtained commercially, or can be prepared from suitable starting materials using methods known in the art.
- the catalysts employed for the current invention may be used in the form of powders, granules, or other particulate forms. Selection of an optimal average particle size for the catalyst will depend upon such process parameters as reactor residence time and desired reactor flow rates. Examples of methods of using base catalysts to convert ethanol to butanol are discussed in the following references.
- U.S. Pat. No. 5,300,695 assigned to Amoco Corp. discloses processes in which an alcohol having X carbon atoms is reacted over an L-type zeolite catalyst to produce a higher molecular weight alcohol.
- a first alcohol having X carbon atoms is condensed with a second alcohol having Y carbon atoms to produce an alcohol having X+Y carbons.
- ethanol is used to produce butanol using a potassium L-type zeolite.
- PCT Publ. No. WO 2006059729 (assigned to Kabushiki Kaisha Sangi) describes a clean process for efficiently producing, from ethanol as a raw material, higher molecular weight alcohols having an even number of carbon atoms, such as 1-butanol, hexanol and the like.
- the higher molecular weight alcohols are yielded from ethanol as a starting material with the aid of a calcium phosphate compound, e.g., hydroxyapatite Ca- ⁇ o(PO 4 ) 6 (OH) 2 , tricalcium phosphate Ca 3 (PO 4 ) 2 , calcium monohydrogen phosphate CaHPO 4 ⁇ (0-2)H 2 O, calcium diphosphate Ca 2 P 2 O 7 , octacalcium phosphate Ca 8 H 2 (P ⁇ 4 ) 6 ⁇ 5H 2 O, tetracalcium phosphate Ca 4 (PO 4 J 2 O, or amorphous calcium phosphate Ca 3 (P ⁇ 4 ) 2 ⁇ nH 2 O, preferably hydroxyapatite, as a catalyst, the contact time being 0.4 second or longer.
- a calcium phosphate compound e.g., hydroxyapatite Ca- ⁇ o(PO 4 ) 6 (OH) 2 , tricalcium phosphate Ca 3 (PO 4 )
- the catalytic conversion of the wet ethanol to the first reaction product comprising 1-butanol and water can be run in either batch or continuous mode as described, for example, in H. Scott Fogler, (Elements of Chemical Reaction Engineering, 2 nd Edition, (1992) Prentice-Hall Inc, CA).
- Suitable reactors include fixed-bed, adiabatic, fluid-bed, transport bed, and moving bed.
- the catalyst may become fouled, and therefore it may be necessary to regenerate the catalyst.
- Preferred methods of catalyst regeneration include, contacting the catalyst with a gas such as, but not limited to, air, steam, hydrogen, nitrogen or combinations thereof, at an elevated temperature.
- a gas such as, but not limited to, air, steam, hydrogen, nitrogen or combinations thereof
- the first reaction product is then subjected to a suitable refining process to produce a partially-purified first reaction product consisting essentially of 1-butanol and no more than 5 weight percent water, based on the weight of the 1-butanol and water combined.
- a suitable refining process may include phase separation (depending on the product mix) followed by distillation of the organic phase to recover a material whose organic content is predominantly 1-butanol. If the material contains more than 5 weight percent water, the material can be further distilled to reduce the water content to no more than 5 weight percent, thereby producing the partially-purified first reaction product.
- the present invention relates to a process for making at least one butene comprising contacting the partially-purified first reaction product consisting essentially of 1-butanol and no more than about 5 weight percent water based on the weight of the 1-butanol and water combined with at least one acid catalyst to produce a second reaction product comprising at least one butene, and recovering said at least one butene from said second reaction product to obtain at least one recovered butene.
- the term "butene” includes 1 -butene, isobutene, and/or cis and trans 2-butene.
- the reaction to form at least one butene is performed at a temperature of from about 50 degrees Celsius to about 450 degrees Celsius. In a more specific embodiment, the temperature is from about 100 degrees Celsius to about 250 degrees Celsius.
- the reaction can be carried out under an inert atmosphere at a pressure of from about atmospheric pressure (about 0.1 MPa) to about 20.7 MPa. In a more specific embodiment, the pressure is from about 0.1 MPa to about 3.45 MPa.
- Suitable inert gases include nitrogen, argon and helium.
- the reaction can be carried out in liquid or vapor phase and can be run in either batch or continuous mode as described, for example, in H. Scott Fogler, (Elements of Chemical Reaction Engineering, 2 nd Edition, (1992) Prentice-Hall Inc, CA).
- the at least one acid catalyst can be a homogeneous or heterogeneous catalyst.
- Homogeneous catalysis is catalysis in which all reactants and the catalyst are molecularly dispersed in one phase.
- Homogeneous acid catalysts include, but are not limited to inorganic acids, organic sulfonic acids, heteropolyacids, fluoroalkyl sulfonic acids, metal sulfonates, metal trifluoroacetates, compounds thereof and combinations thereof.
- homogeneous acid catalysts include sulfuric acid, fluorosulfonic acid, phosphoric acid, p-toluenesulfonic acid, benzenesulfonic acid, hydrogen fluoride, phosphotungstic acid, phosphomolybdic acid, and trifluoromethanesulfonic acid.
- Heterogeneous catalysis refers to catalysis in which the catalyst constitutes a separate phase from the reactants and products.
- Heterogeneous acid catalysts include, but are not limited to 1 ) heterogeneous heteropolyacids (HPAs), 2) natural clay minerals, such as those containing alumina or silica, 3) cation exchange resins, 4) metal oxides, 5) mixed metal oxides, 6) metal salts such as metal sulfides, metal sulfates, metal sulfonates, metal nitrates, metal phosphates, metal phosphonates, metal molybdates, metal tungstates, metal borates, 7) zeolites, and 8) combinations of groups 1 - 7.
- HPAs heterogeneous heteropolyacids
- natural clay minerals such as those containing alumina or silica
- 3) cation exchange resins such as those containing alumina or silica
- metal oxides such as those containing
- the heterogeneous acid catalyst may also be supported on a catalyst support.
- a support is a material on which the acid catalyst is dispersed.
- Catalyst supports are well known in the art and are described, for example, in Satterfield, C. N. (Heterogeneous Catalysis in Industrial Practice, 2 nd Edition, Chapter 4 (1991) McGraw-Hill, New York).
- the reaction is carried out using a heterogeneous catalyst, and the temperature and pressure are chosen so as to maintain the reactant and reaction product in the vapor phase.
- the reactant is obtained from a fermentation broth that is subjected to distillation to produce a vapor phase having at least about 42% water.
- the vapor phase is directly used as a reactant in a vapor phase reaction in which the acid catalyst is a heterogeneous catalyst, and the temperature and pressure are chosen so as to maintain the reactant and reaction product in the vapor phase. It is believed that this vapor phase reaction would be economically desirable because the vapor phase is not first cooled to a liquid prior to performing the reaction.
- the catalyst can be separated from the reaction product by any suitable technique known to those skilled in the art, such as decantation, filtration, extraction or membrane separation (see Perry, R. H. and Green, D.W. (eds), Perry's Chemical Engineer's Handbook, 7 th Edition, Section 13, 1997, McGraw-Hill, New York, Sections 18 and 22).
- the at least one recovered butene is useful as an intermediate for the production of linear, low density polyethylene (LLDPE) or high density polyethylene (HDPE), as well as for the production of transportation fuels and fuel additives.
- butenes can be used to produce alkylate, a mixture of highly branched alkanes, mainly isooctane, having octane numbers between 92 and 96 RON (research octane number) (Kumar, P., et al (Energy & Fuels (2006) 20:481-487).
- isobutene is converted to methyl t-butyl ether (MTBE).
- MTBE methyl t-butyl ether
- butenes are useful for the production of alkyl aromatic compounds.
- Butenes can also be dimerized to isooctenes and further converted to isooctanes, isooctanols and isooctyl alkyl ethers that can be used as fuel additives to enhance the octane number of the fuel.
- the present invention involves contacting the at least one recovered butene with at least one straight-chain, branched or cyclic C 3 to C 5 alkane in the presence of at least one acid catalyst to produce a reaction product comprising at least one isoalkane.
- the acid catalysts useful for these reactions have been homogeneous catalysts, such as sulfuric acid or hydrogen fluoride, or heterogeneous catalysts, such as zeolites, heteropolyacids, metal halides, Bronsted and Lewis acids on various supports, and supported or unsupported organic resins.
- the reaction conditions and product selectivity are dependent on the catalyst.
- the reactions are carried out at a temperature between about -20 degrees C and about 300 degrees C, and at a pressure of about 0.1 MPa to about 10 MPa.
- the at least one isoalkane produced by the reaction can be recovered by distillation (see Seader, J. D., supra) and added to a transportation fuel. Unreacted butenes or alkanes can be recycled and used in subsequent reactions to produce isoalkanes.
- the present invention involves contacting the at least one recovered butene with benzene, a Ci to C 3 alkyl-substituted benzene, or combination thereof, in the presence of at least one acid catalyst or at least one basic catalyst to produce a reaction product comprising at least one C 10 to C ⁇ substituted aromatic compound.
- Ci to C 3 alkyl-substituted benzenes include toluene, xylenes, ethylbenzene and trimethyl benzene.
- acid catalysts promote the addition of butenes to the aromatic ring itself.
- Typical acid catalysts are homogenous catalysts, such as sulfuric acid, hydrogen fluoride, phosphoric acid, AICb and boron fluoride, or heterogeneous catalysts, such as alumino-silicates, clays, ion-exchange resins, mixed oxides, and supported acids.
- heterogeneous catalysts include 2SM-5, Amberlyst® (Rohm and Haas, Philadelphia, PA) and Nafion®-silica (DuPont, Wilmington, DE).
- Typical basic catalysts are basic oxides, alkali-loaded zeolites, organometallic compounds such as alkyl sodium, and metallic sodium or potassium. Examples include alkali-cation- exchanged X- and Y-type zeolites, magnesium oxide, titanium oxide, and mixtures of either magnesium oxide or calcium oxide with titanium dioxide.
- the at least one C1 0 to C 13 substituted aromatic compound produced by the reaction can be recovered by distillation (see Seader, J. D., supra) and added to a transportation fuel. Unreacted butenes, benzene or alkyl-substituted benzene can be recycled and used in subsequent reactions to produce substituted aromatic compounds.
- the present invention involves contacting the at least one recovered butene with methanol, ethanol, a C 3 to C 15 straight- chain, branched or cyclic alcohol, or a combination thereof, in the presence of at least one acid catalyst, to produce a reaction product comprising at least one butyl alkyl ether.
- the "butyl” group can be 1 -butyl, 2-butyl or isobutyl, and the "alkyl” group can be straight-chain, branched or cyclic.
- the reaction of alcohols with butenes is well known and is described in detail by St ⁇ we, A.
- methyl-t-butyl ether MTBE
- TAME methyl-t-amyl ether
- butenes are reacted with alcohols in the presence of an acid catalyst, such as an ion exchange resin.
- the etherification reaction can be carried out at pressures of about 0.1 to about 20.7 MPa, and at temperatures from about 50 degrees Celsius to about 200 degrees Celsius.
- the at least one butyl alkyl ether produced by the reaction can be recovered by distillation (see Seader, J. D., supra) and added to a transportation fuel. Unreacted butenes or alcohols can be recycled and used in subsequent reactions to produce butyl alkyl ether.
- the present invention involves dimerizing the at least one recovered butene to isooctenes, and further converting them to isooctanes, isooctanols or isooctyl alkyl ethers, which are useful fuel additives.
- isooctenes, isooctanes and isooctanols are all meant to denote eight-carbon compounds having at least one secondary or tertiary carbon.
- isooctyl alkyl ether is meant to denote a compound, the isooctyl moiety of which contains eight carbons, at least one carbon of which is a secondary or tertiary carbon.
- the dimerization reaction can be carried out as described in U. S. 6,600,081 (Column 3, lines 42 through 63) for the reaction of isobutane and isobutylene to produce trimethylpentanes (TMPs).
- TMPs trimethylpentanes
- the at least one recovered butene is contacted with at least one dimerization catalyst (for example, silica-alumina) at moderate temperatures and pressures and high throughputs to produce a reaction product comprising at least one isooctene.
- Typical operations for a silica-alumina catalyst involve temperatures of about 150 degrees Celsius to about 200 degrees Celsius, pressures of about 2200 kPa to about 5600 kPa, and liquid hourly space velocities of about 3 to 10.
- dimerization processes use either hydrogen fluoride or sulfuric acid catalysts. With the use of the latter two catalysts, reaction temperatures are kept low (generally from about 15 degrees Celsius to about 50 degrees Celsius with hydrogen fluoride and from about 5 degrees Celsius to about 15 degrees Celsius with sulfuric acid) to ensure high levels of conversion.
- the at least one isooctene can be separated from a solid dimerization catalyst, such as silica-alumina, by any suitable method, including decantation.
- the at least one isooctene can be recovered from the reaction product by distillation (see Seader, J. D., supra) to produce at least one recovered isooctene. Unreacted butenes can be recycled and used in subsequent reactions to produce isooctenes.
- the present invention involves contacting the at least one recovered isooctene produced by the dimerization reaction with at least one hydrogenation catalyst in the presence of hydrogen to produce a reaction product comprising at least one isooctane.
- Suitable solvents, catalysts, apparatus, and procedures for hydrogenation in general can be found in Augustine, R. L. (Heterogeneous Catalysis for the Synthetic Chemist, Marcel Decker, New York, 1996, Section 3); the hydrogenation can be performed as exemplified in U.S. Patent Application No. 2005/0054861 , paragraphs 17-36).
- the reaction is performed at a temperature of from about 50 degrees Celsius to about 300 degrees Celsius, and at a pressure of from about 0.1 MPa to about 20 MPa.
- the principal component of the hydrogenation catalyst may be selected from metals from the group consisting of palladium, ruthenium, rhenium, rhodium, iridium, platinum, nickel, cobalt, copper, iron, osmium; compounds thereof; and combinations thereof.
- the catalyst may be supported or unsupported.
- the at least one isooctane can be separated from the hydrogenation catalyst by any suitable method, including decantation.
- the at least one isooctane can then be recovered (for example, if the reaction does not go to completion or if a homogeneous catalyst is used) from the reaction product by distillation (see Seader, J. D., supra) to obtain a recovered isooctane, and added to a transportation fuel.
- the reaction product itself can be added to a transportation fuel. If present, unreacted isooctenes can be used in subsequent reactions to produce isooctanes.
- the present invention involves contacting the at least one recovered isooctene produced by the dimerization reaction with water in the presence of at least one acidic catalyst to produce a reaction product comprising at least one isooctanol.
- the hydration of olefins is well known, and a method to carry out the hydration using a zeolite catalyst is described in U.S. Patent No. 5,288,924 (Column 3, line 48 to Column 7, line 66), wherein a temperature of from about 60 degrees Celsius to about 450 degrees Celsius and a pressure of from about 700 kPa to about 24,500 kPa are used.
- the water to olefin ratio is from about 0.05 to about 30.
- the at least one isooctanol can be separated from the at least one acid catalyst by any suitable method, including decantation.
- the at least one isooctanol can then be recovered from the reaction product by distillation (see Seader, J. D., supra), and added to a transportation fuel.
- the reaction product itself can be added to a transportation fuel.
- Unreacted isooctenes, if present, can be used in subsequent reactions to produce isooctanols.
- the present invention involves contacting the at least one recovered isooctene produced by the dimerization reaction with at least one acid catalyst in the presence of at least one straight-chain or branched C 1 to C 5 alcohol to produce a reaction product comprising at least one isooctyl alkyl ether.
- a reaction product comprising at least one isooctyl alkyl ether.
- C-i and C 2 alcohols cannot be branched.
- The' etherification reaction is described by St ⁇ we, A., et al (Synthesis of MTBE and TAME and related reactions, Section 3.11 , in Handbook of Heterogeneous Catalysis, Volume 4, (Ertl, G., Kn ⁇ zinger, H., and Weitkamp, J.
- Suitable acid catalysts include, but are not limited to, acidic ion exchange resins. Where a solid acid catalyst is used, such as an ion-exchange resin, the at least one isooctyl alkyl ether can be separated from the at least one acid catalyst by any suitable method, including decantation. The at least one isooctyl alkyl ether can then be recovered from the reaction product by distillation (see Seader, J.
- the present invention involves contacting recovered isooctene (as obtained from the dimerization of butenes, see the fifth aspect) with hydrogen in the presence of at least one hydrogenation catalyst to produce a reaction product comprising at least one isooctane and recovering the at least one isooctane from the reaction product to obtain at least one recovered isooctane.
- the recovered isooctane is then contacted with a heterogeneous dehydrocyclization catalyst to produce a reaction product comprising p-xylene, and recovering said p-xylene.
- Suitable catalysts for the catalytic dehydrocyclization of isooctane to p-xylene are generally described in US Pat. No. 7,067,708 (see column 2, line 51 through column 3, line 21.
- the temperature can be from about 300 degrees to about 700 degrees Celsius, and pressures can be from about atmospheric pressure to about 1 MPa.
- the present invention involves contacting recovered isooctene (see fifth aspect) with a heterogeneous dehydrogenation catalyst to produce a reaction product comprising p- xylene.
- Suitable dehydrogenation catalysts are generally described in US Pat. Publ. No. 2005/0228204 A1 (see paragraphs [0018 - 0021]).
- Suitable temperatures are from about 300 degrees to about 700 degrees Celsius, and pressures can be from about atmospheric pressure to about 1MPa.
- the p-xylene thus formed can be subsequently employed in the production of a variety of other products, including but not limited to terephthalic acid and polyesters.
- terephthalic acid is produced by catalytic, liquid-phase air oxidation of p-xylene.
- the catalysts used are generally multivalent heavy metal or metals comprising cobalt. The most popular form of this process uses cobalt and manganese as the multivalent heavy- metal catalysts and bromine as the renewable source for free radicals.
- C is degrees Celsius
- mg is milligram
- ml is milliliter
- m is meter
- mm is millimeter
- min is minute
- temp is temperature
- MPa is mega Pascal
- GC/MS gas chromatography/mass spectrometry.
- Amberlyst® manufactured by Rohm and Haas, Philadelphia, PA
- tungstic acid, 1-butanol and H 2 SO 4 were obtained from Alfa Aesar (Ward Hill, MA)
- CBV-3020E HZSM-5 was obtained from PQ Corporation (Berwyn, PA)
- Sulfated Zirconia was obtained from Engelhard Corporation (Iselin, NJ)
- 13% Nafion®/SiO 2 (SAC-13) can be obtained from Engelhard
- H-Mordenite can be obtained from Zeolyst Intl. (Valley Forge, PA).
- Gamma alumina was obtained from Strem Chemical, Inc. (Newburyport, MA).
- Catalyst was added to 1-butanol (1 ml) in a 2 ml vial equipped with a magnetic stir bar.
- the vial was sealed with a serum cap perforated with a needle to facilitate gas exchange.
- the vial was placed in a block heater enclosed in a pressure vessel. The vessel was purged with nitrogen and the pressure was set as indicated below. The block was brought to the indicated temperature and maintained at that temperature for the time indicated.
- the contents of the vial were analyzed by GC/MS using a capillary column (either (a) CP-Wax 58 [Varian; Palo Alto, CA], 25 m X 0.25 mm, 45 C/6 min, 10 C/min up to 200 C, 200 C /10 min, or (b) DB-1701 [J&W (available through Agilent; Palo Alto, CA)], 3O m X 0.2 5mm, 50 C /10 min, 10 C /min up to 250 C, 250 C /2 min).
- a capillary column either (a) CP-Wax 58 [Varian; Palo Alto, CA], 25 m X 0.25 mm, 45 C/6 min, 10 C/min up to 200 C, 200 C /10 min, or (b) DB-1701 [J&W (available through Agilent; Palo Alto, CA)], 3O m X 0.2 5mm, 50 C /10 min, 10 C /min up to 250 C, 250 C
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
L'invention concerne un procédé de fabrication de butènes et de dérivés de ceux-ci à partir d'éthanol aqueux éventuellement obtenu à partir d'un bouillon de fermentation. Les butènes ainsi produits peuvent être employés en tant qu'intermédiaires dans la fabrication de polyéthylènes et d'autres matériaux utiles connus.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/513,700 US20100036173A1 (en) | 2007-01-09 | 2007-11-30 | Production of butenes and derivatives therefrom from aqueous ethanol |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US87236406P | 2006-12-01 | 2006-12-01 | |
US60/872,364 | 2006-12-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008069985A1 true WO2008069985A1 (fr) | 2008-06-12 |
Family
ID=39492537
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2007/024669 WO2008069985A1 (fr) | 2006-12-01 | 2007-11-30 | Fabrication de butènes et de dérivés de ceux-ci à partir d'éthanol aqueux |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2008069985A1 (fr) |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4196136A (en) * | 1978-11-06 | 1980-04-01 | E. I. Du Pont De Nemours And Company | Ligated transition metal derivatives of heteropolyanions |
US4891465A (en) * | 1986-11-11 | 1990-01-02 | Mitsui Petrochemical Industries, Ltd. | Process for producting alkyl group-substituted aromatic hydrocarbons |
US5070016A (en) * | 1991-03-28 | 1991-12-03 | Revolution Fuels Of America, Inc. | Integrated process for producing ethanol, methanol and butyl ethers |
US5288924A (en) * | 1992-09-18 | 1994-02-22 | Mobil Oil Corporation | Process for starting up an olefin hydration reactor |
US5300695A (en) * | 1992-12-07 | 1994-04-05 | Amoco Corporation | Process for preparing alcohols |
US5563299A (en) * | 1994-02-11 | 1996-10-08 | Enichem S.P.A | Integrated process for the simultaneous production of alkyl tert-butyl ethers and 1-butene |
US6103947A (en) * | 1994-12-23 | 2000-08-15 | Uop Llc | Alkylation of alkanes with mixtures of alkenes and alkyl halides |
US20050137435A1 (en) * | 2003-12-22 | 2005-06-23 | Marja Tiitta | Process for producing gasoline components |
US20050228204A1 (en) * | 2003-11-25 | 2005-10-13 | Manzer Leo E | Process for the preparation of xylene |
US7067708B2 (en) * | 2000-03-16 | 2006-06-27 | E. I. Du Pont De Nemours And Company | Process for the preparation of p-xylene |
-
2007
- 2007-11-30 WO PCT/US2007/024669 patent/WO2008069985A1/fr active Application Filing
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4196136A (en) * | 1978-11-06 | 1980-04-01 | E. I. Du Pont De Nemours And Company | Ligated transition metal derivatives of heteropolyanions |
US4891465A (en) * | 1986-11-11 | 1990-01-02 | Mitsui Petrochemical Industries, Ltd. | Process for producting alkyl group-substituted aromatic hydrocarbons |
US5070016A (en) * | 1991-03-28 | 1991-12-03 | Revolution Fuels Of America, Inc. | Integrated process for producing ethanol, methanol and butyl ethers |
US5288924A (en) * | 1992-09-18 | 1994-02-22 | Mobil Oil Corporation | Process for starting up an olefin hydration reactor |
US5300695A (en) * | 1992-12-07 | 1994-04-05 | Amoco Corporation | Process for preparing alcohols |
US5563299A (en) * | 1994-02-11 | 1996-10-08 | Enichem S.P.A | Integrated process for the simultaneous production of alkyl tert-butyl ethers and 1-butene |
US6103947A (en) * | 1994-12-23 | 2000-08-15 | Uop Llc | Alkylation of alkanes with mixtures of alkenes and alkyl halides |
US7067708B2 (en) * | 2000-03-16 | 2006-06-27 | E. I. Du Pont De Nemours And Company | Process for the preparation of p-xylene |
US20050228204A1 (en) * | 2003-11-25 | 2005-10-13 | Manzer Leo E | Process for the preparation of xylene |
US20050137435A1 (en) * | 2003-12-22 | 2005-06-23 | Marja Tiitta | Process for producing gasoline components |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20100029994A1 (en) | Production of butenes and derivatives therefrom from dry ethanol | |
KR101688254B1 (ko) | Mtbe 분해에 의한 이소부텐의 제조 | |
DK2547639T3 (en) | Producing propylene VIA THE SAME TIME dehydration and skeletal isobutanol ON ACID CATALYSTS FOLLOWED BY META TESE | |
US20080015395A1 (en) | Process for making butenes from aqueous 1-butanol | |
US20080045754A1 (en) | Process for making butenes from dry 1-butanol | |
US20080132730A1 (en) | Process for making butenes from dry 2-butanol | |
US20100174121A1 (en) | Production of butenes and derivatives therefrom from dry ethanol | |
US20090030239A1 (en) | Process for making butenes from aqueous isobutanol | |
WO2008016428A2 (fr) | Procédé permettant de fabriquer des butènes à partir d'isobutanol sec | |
CA2668036A1 (fr) | Procede de fabrication de butenes a partir de 2-butanol aqueux | |
Macho et al. | Dehydration of C4 alkanols conjugated with a positional and skeletal isomerisation of the formed C4 alkenes | |
US20100036173A1 (en) | Production of butenes and derivatives therefrom from aqueous ethanol | |
US8398728B2 (en) | Process for making a composition comprising at least two different dialkyl ethers | |
US20100168478A1 (en) | Production of butenes and derivatives therefrom from aqueous ethanol | |
CA2668889A1 (fr) | Procede de fabrication de dibuthylethers a partir d'ethanol sec | |
WO2008069985A1 (fr) | Fabrication de butènes et de dérivés de ceux-ci à partir d'éthanol aqueux | |
CA2668878A1 (fr) | Procede de preparation d'ethers de dibutyle a partir d'ethanol aqueux | |
CA2668876A1 (fr) | Procede de preparation d'ethers de dibutyle a partir d'ethanol aqueux | |
CA2668877A1 (fr) | Procede de preparation d'ethers de dibutyle a partir d'ethanol deshydrate |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 07862381 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12513700 Country of ref document: US |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 07862381 Country of ref document: EP Kind code of ref document: A1 |