US20150361565A1 - Conversion of Carboxylic Acids to Alpha-Olefins - Google Patents

Conversion of Carboxylic Acids to Alpha-Olefins Download PDF

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US20150361565A1
US20150361565A1 US14/730,413 US201514730413A US2015361565A1 US 20150361565 A1 US20150361565 A1 US 20150361565A1 US 201514730413 A US201514730413 A US 201514730413A US 2015361565 A1 US2015361565 A1 US 2015361565A1
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carboxylic acid
alkali metal
olefins
alkali
acid
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James M. Mosby
Patrick McGuire
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Enlighten Innovations Inc
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Ceramatec Inc
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Assigned to ENLIGHTEN INNOVATIONS INC. reassignment ENLIGHTEN INNOVATIONS INC. MERGER AND CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: ENLIGHTEN INNOVATIONS INC., FIELD UPGRADING LIMITED
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    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
    • C25B9/17—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof
    • C25B9/19—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/20—Processes
    • C25B3/25—Reduction
    • C25B9/08—
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B1/00—Electrolytic production of inorganic compounds or non-metals
    • C25B1/01—Products
    • C25B1/02—Hydrogen or oxygen
    • C25B1/04—Hydrogen or oxygen by electrolysis of water
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B15/00—Operating or servicing cells
    • C25B15/02—Process control or regulation
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/20—Processes
    • C25B3/23—Oxidation
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
    • C25B9/17—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof
    • C25B9/19—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms
    • C25B9/23—Cells comprising dimensionally-stable non-movable electrodes; Assemblies of constructional parts thereof with diaphragms comprising ion-exchange membranes in or on which electrode material is embedded
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30—Hydrogen technology
    • Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P30/00—Technologies relating to oil refining and petrochemical industry
    • Y02P30/20—Technologies relating to oil refining and petrochemical industry using bio-feedstock

Definitions

  • the present application relates to methods of preparing olefins from carboxylic acids, particularly using electrolytic techniques.
  • High quality synthetic based oil is mainly composed of poly-alpha-olefins (PAOs), for which market demand outweighs available supply.
  • PAOs poly-alpha-olefins
  • the disparity between the supply and demand for PAOs arises because the necessary starting material is made using fractions of petroleum that are used in the production of kerosene and diesel. In most crude oil refineries, the later products take priority over the PAOs, and thus limited amounts of these fractions are diverted to make PAOs.
  • an electrochemical method of preparing olefins from an alkali metal salt of a carboxylic acid includes providing an electrochemical cell having an anolyte compartment, a catholyte compartment, and an alkali ion conductive membrane separating the anolyte compartment from the catholyte compartment.
  • the method further includes providing an anolyte solution of an alkali metal salt of the carboxylic acid to the anolyte compartment.
  • the anolyte solution may have a pH in the range from about 8 to 14.
  • An electrical potential is applied to the anode and cathode to electrochemically decarboxylate the alkali metal salt of the carboxylic acid into one or more olefins.
  • the anolyte compartment comprises an electrochemically active anode selected to perform a two-electron decarboxylation reaction of the alkali metal salt of the carboxylic acid, wherein the anode comprises a carbonaceous surface.
  • the catholyte compartment comprises an electrochemically active cathode where reduction reactions occur.
  • the alkali ion conductive membrane permits selective transport of alkali ions between the anolyte compartment and the catholyte compartment under influence of the electric potential.
  • the current has a voltage between 2 and 20 volts. In other embodiments, the voltage is between 4 and 12 volts. In some embodiments, the current has a current density of between 5 and 100 mA/cm 2 . In other embodiments, the current density is between 5 and 50 mA/cm 2 . In some embodiments, the carboxylic acid is neutralized to have a pH between about 8 and 14. In other embodiments, the pH is between 9 and 13. In still other embodiments, the pH is between 10 and 12.
  • the method also includes mixing the alkali metal salt of the carboxylic acid with an organic solvent.
  • the organic solvent comprises one or more organic alcohols and mixtures thereof.
  • the one or more organic alcohols are selected from the group consisting of: methanol, ethanol, propanol, isopropanol, butanol, and mixtures thereof.
  • the organic solvent is selected form the group consisting of: acetonitrile, dimethylformamide, sulfolane, pyridine, 2,6-pyridine, and mixtures of the same.
  • the method also includes adjusting the pH of the alkali metal salt of the carboxylic acid with a base.
  • the base is an alkali metal hydroxide.
  • the base is sodium hydroxide.
  • the method also includes mixing the alkali metal salt of the carboxylic acid with an electrolyte selected from the group consisting of: a metal halide, a metal nitrate, a metal sulfate, a metal perchlorate, and a metal tetrafluoroborate.
  • an electrolyte selected from the group consisting of: a metal halide, a metal nitrate, a metal sulfate, a metal perchlorate, and a metal tetrafluoroborate.
  • the alkali ion conducting membrane is a NaSICON membrane.
  • the method also includes fermenting biomass to produce the carboxylic acid and neutralizing the carboxylic acid with an alkali metal hydroxide to form the alkali metal salt of the carboxylic acid.
  • the carboxylic acid may have an even number of carbon atoms.
  • the carboxylic acid is selected from the group consisting of: octanoic acid, decanoic acid, dodecanoic acid, tetradecanoic acid, hexadecanoic acid, and octadecanoic acid.
  • the carboxylic acid is dodecanoic acid.
  • the one or more olefins is an alpha-olefin. In some embodiments, the one or more olefins is 1-undecene. In another aspect, a method further comprises oligomerizing the one or more olefins to make a synthetic lubricant.
  • an electrochemical cell or reactor for producing olefins in another aspect, includes an anolyte compartment, a catholyte compartment, an alkali ion conductive membrane, and a source of electric potential to operate the electrochemical reactor.
  • the anolyte compartment includes a solution of an alkali metal salt of a carboxylic acid.
  • the solution has a pH in the range from about 8 to 14, and preferably a pH in the range from 9 to 13, and more preferably a pH in the range from about 10 to 12.
  • the anolyte compartment includes an electrochemically active anode selected to perform a two-electron decarboxylation reaction of the alkali metal salt of carboxylic acid.
  • the anode comprises a carbonaceous surface.
  • the catholyte compartment houses an electrochemically active cathode where reduction reactions occur.
  • the alkali ion conductive membrane separates the anolyte compartment from the catholyte compartment and permits selective transport of alkali ions between the anolyte compartment and the catholyte compartment.
  • the source of electric potential is electrically connected to the anode and to the cathode.
  • FIG. 1 is a schematic representation of a possible electrochemical reactor that may be used in the disclosed method of preparing olefins from carboxylic acids.
  • FIG. 2A is a graph showing voltage and current density verses time for comparative one electron decarboxylation of sodium octanoate to a hydrocarbon dimer coupling product.
  • FIG. 2B is a gas chromatograph showing the resulting products from applying voltage and current densities for the decarboxylation process from FIG. 2A .
  • FIG. 3A is a graph showing voltage and current density verses time for a two electron decarboxylation of sodium dodecanoate to olefins.
  • FIG. 3B is a chromatograph showing the resulting products from applying voltage and current densities for the decarboxylation process from FIG. 3A .
  • the present disclosure describes an economically viable and novel upgrading process to produce olefins from carboxylic acids, including biomass, without using hydrogen gas or expensive catalysis.
  • the present technique is used for the production of alpha-olefins.
  • the olefins produced can be a direct replacement of the olefins synthesized from crude oil for a variety of applications, including but not limiting to co-monomers, PAO synthetic lubricants, drilling lubricants, and surfactants.
  • the method disclosed can selectively produce specific olefins with yields above 50% at moderate temperatures and pressures and without the use of a catalyst.
  • hydrogen gas can be concurrently produced in an electrochemical reactor such as with a two-compartment cell. This hydrogen can be recovered and used for other processes that require hydrogen input.
  • the innovation can produce bio-derived olefins that are just an alternative to petroleum based olefins, but at an economical advantage.
  • GHG green-house gas
  • the process uses an electrochemical reactor that converts an alkali metal salt of lauric acid (a twelve-carbon (C12) carboxylic acid), optionally produced from the fermentation of lignocellulose sugar, into a corresponding alpha-olefin, for example 1-undecene (also known as undec-1-ene).
  • lauric acid a twelve-carbon (C12) carboxylic acid
  • the oxidation is carried out in a simple electrochemical reactor that can be used on a distributed scale, following the two electron oxidation reaction represented as:
  • metal (M) is sodium as:
  • the process described herein is a two electron decarboxylation.
  • a one electron decarboxylation process is known as Kolbe electrolysis that results in radical coupling products that are undesirable according to the presently disclosed invention.
  • two electron decarboxylation to produce olefins is desired according to the present invention, whereas one electron decarboxylation to produce radical coupling products is not desired.
  • the alkali metal ions for example sodium-ions, react with hydroxide anions produced by the corresponding reduction of water in the reaction shown below.
  • the alkali hydroxide may optionally be used to saponify the feedstock carboxylic acid to form the alkali metal salt of the carboxylic acid as follows:
  • the alkali hydroxide may be regenerated in the catholyte compartment as described above.
  • FIG. 1 schematically shows one possible electrochemical cell or reactor 100 that may be used in the electrochemical process of producing olefins within the scope of the present invention.
  • the electrolytic cell 100 includes an anolyte compartment 110 , a catholyte compartment 112 , and an alkali ion conductive membrane 114 separating the anolyte compartment 110 from the catholyte compartment 112 .
  • the anolyte compartment 110 comprises an electrochemically active anode 116 selected to perform a two-electron decarboxylation reaction of an alkali metal salt of a carboxylic acid.
  • the anode 116 preferably comprises a carbonaceous surface.
  • the catholyte compartment 112 comprises an electrochemically active cathode 118 where reduction reactions occur.
  • the alkali ion conductive membrane 114 permits selective transport of alkali ions (M + ) 120 between the anolyte compartment 110 and the catholyte compartment 112 under influence of an electric potential 122 while preventing solvent or anion transfer between the anolyte and catholyte compartments.
  • Alkali ions 120 include, but are not limited to, sodium ions, lithium ions, potassium ions and mixtures of the same.
  • the alkali ion conductive membrane 114 can be virtually any suitable alkali ion conductive membrane that selectively conducts alkali ions and prevents the passage of water, hydroxide ions, or other reaction products.
  • the alkali ion conducting membrane 114 may include a ceramic, a polymer, or combinations thereof.
  • the alkali ion conducting membrane is an alkali ion super ion conducting (MSICON) membrane.
  • MSICON alkali ion super ion conducting
  • Some non-limiting examples of such membranes include, but are not limited to, a NaSICON (sodium super ionic conductor membrane) and a NaSICON-type membrane.
  • the alkali ion conductive membrane may be any of a number of sodium super ion conducting materials, including, without limitation, those disclosed in United States Patent Application Publications Nos. 2010/0331170 and 2008/0245671 and in U.S. Pat. No. 5,580,430. The foregoing applications and patent are hereby incorporated by reference.
  • a sodium selective ceramic membrane NaSelect® (Ceramatec, Salt Lake City, Utah USA) may be used.
  • alkali ion conductive membranes such as a LiSICON membrane, a LiSICON-type membrane, a KSICON membrane, a KSICON-type membrane may be used.
  • an alkali ion conducting ion-exchange polymeric membrane may be used.
  • the alkali ion conducting membrane may comprise an alkali ion conductive glass or beta alumina.
  • the electrochemical cell 100 may be a parallel plate configuration where flat plate electrodes and membranes are used.
  • the anode 116 can be any suitable anode material that allows two-electron oxidation (decarboxylation) reaction in the anolyte compartment 110 when electrical potential 122 passes between the anode 116 and the cathode 118 .
  • suitable anode materials include carbonaceous electrodes or electrodes with carbonaceous surfaces such as natural or artificial graphite, graphite nanopowder, acetylene black, Super P® (available from Westlake Chemical, Westlake, Ohio), MesoCarbon, high surface active carbon, glassy carbon, carbon nanotubes, and graphene.
  • the cathode 118 may be any suitable cathode that allows the cell to reduce water, methanol, or other suitable electrolyte containing-solvent in the catholyte compartment 112 to produce hydroxide ions, methoxide ions, or other corresponding organic oxide ions and hydrogen gas.
  • suitable cathode materials include, without limitation, nickel, stainless steel, graphite, and any other suitable cathode material that is known or novel.
  • the electrolytic cell 100 is operated by feeding or otherwise providing an anolyte solution 124 into the anolyte compartment 110 .
  • the anolyte solution 124 includes a solvent and a carboxylic acid or an alkali metal salt of carboxylic acid.
  • the alkali metal salt of the carboxylic acid can be obtained by reacting the carboxylic acid with alkali metal hydroxide, for example sodium hydroxide (NaOH), lithium hydroxide (LiOH), and potassium hydroxide (KOH).
  • the carboxylic acid can be obtained from a variety of sources, including biomass.
  • suitable carboxylic acids are fatty acids listed in Table 1.
  • the carboxylic acid has from 6-20 carbon atoms.
  • the carboxylic acid has from 6-12 carbon atoms.
  • the carboxylic acid has from 16-18 carbon atoms.
  • the carboxylic acid has from 12-18 carbon atoms.
  • the resulting olefins have from 5-19 carbon atoms. In some embodiments, the olefins have from 5-11 carbon atoms. In some embodiments, the olefins have from 15-17 carbon atoms. In some embodiments, the olefins have from 11-17 carbon atoms.
  • the anolyte solution 124 may include one or more solvents.
  • the solvent may be an organic lower alkanol such as methanol, ethanol, propanol, isopropanol, butanol, or mixtures of the same.
  • the solvent may be acetonitrile, dimethylformamide, sulfolane, pyridine, 2,6-pyridine, and mixtures of the same.
  • the solvent may be comprised of an ionic liquid. In other embodiments that solvent may be comprised of a molten salt.
  • the anolyte solution 124 may optionally contain a supporting electrolyte that is soluble in the solvent and which provides high electrolyte conductivity in the anolyte solution.
  • a supporting electrolyte includes an alkali metal tetrafluoroborate. Another example may include tetramethylammonium hexafluorophosphate. Other ionic solids may also be used such as metal halides, nitrates, sulfates, perchlorates, and mixtures of the same.
  • supporting electrolytes that act as a Br ⁇ nsted base are used. In such a case, the supporting electrolyte not only increases the conductivity of the anolyte solution, it also increases the rate of the olefin formation by promoting an E1 elimination reaction.
  • An electrical potential 122 is applied to the anode 116 and cathode 118 to electrochemically decarboxylate the alkali metal salt of the carboxylic acid into one or more olefins 126 and carbon dioxide (CO 2 ) 128 .
  • the olefins produced include alpha olefins and internal linear olefins. The carbon number of the olefin produced depends on the carboxylic acid or alkali carboxylate salts used in the decarboxylation.
  • the decarboxylation of laurate (C12) produces the C11 alpha-olefin, 1-undecene, and also the internal linear olefins such as 2-undecene, 3-undecene, 4-undecene, and 5-undecene, and mixtures of the same.
  • the electric potential 122 may be applied at a voltage of between 2 and 30 V. In some embodiments, the voltage applied is between 4 and 18 V. In some embodiments, the voltage applied is between 4 and 12 V.
  • the electric potential may be applied with a current density of between 5 and 100 mA/cm 2 . In some embodiments, the current density is between 5 and 50 mA/cm 2 .
  • the anolyte solution 110 has a pH in the range from about 8 to 14. In other embodiments, the anolyte solution 110 has a pH in the range from about 9 to 13. In still other embodiments, the anolyte solution 110 has a pH in the range from about 10 to 12. It should be understood by those of ordinary skill that the electrical potential, current density, and pH can be controlled to modify the ratio of olefins produced by the electrochemical decarboxylation.
  • the anolyte compartment may have an operating temperature in the range from 20° C. to 150° C. In other embodiments, the anolyte compartment may have an operating temperature in the range from 50° C. to 150° C. It is believed that a temperature greater than ambient temperature (>20° C.) may facilitate the decarboxylation reaction to produce olefins.
  • a catholyte solution 130 is provided into the catholyte compartment 112 .
  • the catholyte solution 130 may comprise a solvent that is the same or different than the anolyte solvent.
  • the anolyte and catholyte solvents may be different because the alkali conductive membrane 114 isolates the compartments and from each other.
  • the catholyte solvent may comprise a mixture of solvents with or without water.
  • the catholyte solution comprises water.
  • the catholyte solution includes alkali ions, which may be in the form of an unsaturated alkali hydroxide solution.
  • the concentration of alkali hydroxide can be between about 0.1% by weight and about 50% by weight of the solution.
  • the catholyte solution includes a dilute solution of alkali hydroxide.
  • the source of alkali ions may be provided by alkali ions transporting across the alkali ion conductive membrane from the anolyte compartment to the catholyte compartment.
  • alkali hydroxide is used in the following discussion and shown in FIG. 1 , persons skilled in the art will appreciate that methanol may substitute alkali hydroxide in the apparatus for preparing alkali methylate instead.
  • the catholyte solution may include methanol.
  • reaction 1 reduction of water to form hydrogen gas 132 and hydroxide ions takes place (Reaction 1).
  • the hydroxide ions react with available alkali ions (M + ) 120 transported from anode compartment 110 via the alkali conductive membrane 114 to form alkali hydroxide as shown in Reaction 2.
  • the alkali hydroxide 134 may be recovered from the catholyte compartment 112 .
  • the catholyte solution comprises a base which may be used to neutralize the carboxylic acid to produce the alkali metal salt of the carboxylic acid.
  • the base consumed in the acid neutralization step may be produced in the catholyte compartment, recovered, and re-used in acid neutralization reactions or other chemical processes.
  • the electrolytic cell may be operated in a continuous mode.
  • a continuous mode the cell is initially filled with anolyte solution and catholyte solution and then, during operation, additional solutions are fed into the cell and products, by-products, and/or diluted solutions are removed from the cell without ceasing operation of the cell.
  • the feeding of the anolyte solution and catholyte solution may be done continuously or it may be done intermittently, meaning that the flow of a given solution is initiated or stopped according to the need for the solution and or to maintain desired concentrations of solutions in the cell compartments, without emptying any one individual compartment or any combination of the two compartments.
  • the removal of solutions from the anolyte compartment and the catholyte compartment may also be continuous or intermittent.
  • Control of the addition and or removal of solutions from the cell may be done by any suitable means.
  • Such means include manual operation, such as by one or more human operators, and automated operation, such as by using sensors, electronic valves, laboratory robots, etc. operating under computer or analog control.
  • automated operation a valve or stopcock may be opened or closed according to a signal received from a computer or electronic controller on the basis of a timer, the output of a sensor, or other means. Examples of automated systems are well known in the art. Some combination of manual and automated operation may also be used.
  • the amount of each solution that is to be added or removed per unit time to maintain a steady state may be experimentally determined for a given cell, and the flow of solutions into and out of the system set accordingly to achieve the steady state flow conditions.
  • the electrolytic cell is operated in batch mode.
  • batch mode the anolyte solution and catholyte solution are fed initially into the cell and then the cell is operated until the desired concentration of product is produced in the anolyte and catholyte. The cell is then emptied, the products collected, and the cell refilled to start the process again.
  • combinations of continuous mode and batch mode production may be used.
  • the feeding of solutions may be done using a pre-prepared solution or using components that form the solution in situ.
  • both continuous and batch mode have dynamic flow of solutions.
  • the anolyte solution is added to the anolyte compartment so that the sodium concentration is maintained at a certain concentration or concentration range during operation of the electrolytic cell.
  • a certain quantity of alkali ions are transferred through the alkali ion conductive membrane to the catholyte compartment and are not replenished, with the cell operation is stopped when the alkali ion concentration in the anolyte compartment reduces to a certain amount or when the appropriate product concentration is reached in the catholyte compartment.
  • the resulting alpha-olefins may be oligomerized to poly-alpha olefins (PAOs) by conventional techniques to synthetic oils.
  • PAOs poly-alpha olefins
  • the C11 olefins are oligomerized to produce poly-internal-olefins (PIOs) by conventional techniques and thereby produce synthetic oil.
  • the entire process is hydrogen-independent. In some embodiments, the process requires small amounts of electricity.
  • the electrochemical reactor can be commercialized for distributed manufacturing of the olefins.
  • the sodium salt of lauric acid obtained from fermentation from biomass can be directly fed into the membrane reactor, thereby obviating the need for any separation or purification.
  • the electrochemical reactor uses inexpensive electrode materials with low power consumption.
  • the resulting alpha-olefins are oligomerized to produce a synthetic bio-lubricant.
  • the examples disclosed herein used an experimental setup which consisted of a micro flow cell, allowing both the anolyte and catholyte to be pumped through the cell while minimizing the distance between the electrodes and the membrane.
  • the membranes used in the examples consisted of 2.54 cm diameter NaSICON disks of about 1 mm thickness that were housed on scaffolds in the center of the cells. As the scaffold and membrane physically separate the anode and cathode compartments, there was a separate reservoir and temperature controlled hotplate for the anolyte and catholyte. This allowed the chemistry and conditions of each electrolyte to be optimized for the respective electrode reactions.
  • a multiple-head peristaltic pump was used to pump both electrolyte solutions into the electrolysis cell. The tubing between the cell, pump, and reservoir was insulated for temperature sensitive electrolytes.
  • the anolyte solution that contains the sodium salt of the carboxylic acid was made by dissolving at least 10% of the salt into a solvent system consisting of different mixtures that contain water, methanol, ethanol, and butanol.
  • the sodium salts were prepared in separate solutions following conventional saponification reactions followed by dissolution of the prepared salt into an electrolyte solution. For this method, a general saponification product was used during which the sodium carboxylate forms as the carboxylic acid is neutralized. The details of the electrolyte preparation will be given in the different examples.
  • the catholyte was made from aqueous sodium hydroxide solutions. To obtain low solution resistance the temperature of the electrolyte were increased to 50° C. to improve both the solubility and conductivity.
  • a power supply was connected and a current density between 10 and 100 mA/cm 2 was applied.
  • the voltage and current were monitored using a Data Acquisition Unit (Agilent 3490A) controlled by LabVIEW software.
  • the applied current density caused oxidation to occur at the anode (smooth platinum or graphite) and reduction to occur at the cathode (nickel), with each electrode having a surface area of 11 cm 2 .
  • the power supply transport electrons from the anode to the cathode, a charge balance must be maintained across the cell by the diffusion or positively charge ions.
  • sodium ions Given the high selectivity of the NaSICON membrane for Na-ions, sodium ions are the only species that can provide this balance. Thus a high concentration of the sodium salts was desired and used.
  • hexane was used to perform liquid-liquid extraction. After the extraction, the olefins were analyzed in the hexane using, IR (Bruker, Tensor 37), GC (Bruker, SICON 465), and GC-MS (Bruker, SCION465 GC-SQ). The olefins could be isolated and purified by removing the hexane using a slight vacuum and low heat affording the recovered olefins at a 98% purity level.
  • the product was extracted/removed from the electrolyte using liquid-liquid extraction with hexane.
  • the product of the electrolysis was then analyzed using GC-MS, producing the GC shown in FIG. 2B . From this it was determined that the product distribution was 80% tetradecane, 5% heptanol, 10% esters, and 5% heptenes.
  • Example 1 The electrolysis conditions from Example 1 were changed to show the selective production of olefins instead of paraffins using the techniques disclosed herein.
  • One difference between the two examples that caused the change in product selectivity was the use of a graphite electrode in this example while a platinum electrode was used in Example 1.
  • 10% sodium laurate was dissolved in an electrolyte containing a mixture of methanol, butanol, and water having a pH of 10.5.
  • the catholyte consisted of 10% aqueous sodium hydroxide.
  • the catholyte and anolyte were heated to 50° C.
  • Electrolysis was conducted in batch mode during which the anolyte and catholyte were cycled through the corresponding anode and cathode compartments of the cell. The cell was operated until enough charge passed to theoretically convert 80% of the sodium laurate.
  • electrolysis was conducted at a constant cell potential of 4 V and a current density of 20 mA/cm 2 .
  • the product was extracted/removed from the electrolyte using liquid-liquid extraction with hexane.
  • the product of the electrolysis was then analyzed using GC-MS, producing the gas chromatogram shown in FIG. 3B . From this it was determined that the product distribution was ⁇ 5% docosane, 40% undecanol, ⁇ 5% esters, and over 50% undecenes. Of the undecenes, 50% corresponded to the alpha-olefin, 1-undecene.
  • the disclosed invention provides an electrochemical method of preparing olefins from alkali metal salts of carboxylic acids.
  • Low-cost, renewable biomass may provide a source of alkali metal salts of carboxylic acids.

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  • Automation & Control Theory (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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US9493882B2 (en) 2010-07-21 2016-11-15 Ceramatec, Inc. Custom ionic liquid electrolytes for electrolytic decarboxylation
US9677182B2 (en) 2011-01-25 2017-06-13 Ceramatec, Inc. Production of fuel from chemicals derived from biomass
US9957622B2 (en) 2009-07-23 2018-05-01 Field Upgrading Limited Device and method of obtaining diols and other chemicals using decarboxylation
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US9752081B2 (en) * 2009-07-23 2017-09-05 Ceramatec, Inc. Method of producing coupled radical products from biomass
US9957622B2 (en) 2009-07-23 2018-05-01 Field Upgrading Limited Device and method of obtaining diols and other chemicals using decarboxylation
US10968525B2 (en) 2009-07-23 2021-04-06 Enlighten Innovations Inc. Device and method of obtaining diols and other chemicals using decarboxylation
US9493882B2 (en) 2010-07-21 2016-11-15 Ceramatec, Inc. Custom ionic liquid electrolytes for electrolytic decarboxylation
US10145019B2 (en) 2010-07-21 2018-12-04 Enlighten Innovations Inc. Custom ionic liquid electrolytes for electrolytic decarboxylation
US9677182B2 (en) 2011-01-25 2017-06-13 Ceramatec, Inc. Production of fuel from chemicals derived from biomass
CN114318388A (zh) * 2022-01-25 2022-04-12 山西大学 一种光电催化烯烃加氢装置及其应用

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EP3155143B1 (en) 2019-12-11
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EP3155143A4 (en) 2018-01-24
BR112016029237A8 (pt) 2018-08-14
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EP3155143A1 (en) 2017-04-19
WO2015191353A1 (en) 2015-12-17

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