WO2014039695A1 - Methods for generating hydrogen gas using plasma sources - Google Patents

Methods for generating hydrogen gas using plasma sources Download PDF

Info

Publication number
WO2014039695A1
WO2014039695A1 PCT/US2013/058287 US2013058287W WO2014039695A1 WO 2014039695 A1 WO2014039695 A1 WO 2014039695A1 US 2013058287 W US2013058287 W US 2013058287W WO 2014039695 A1 WO2014039695 A1 WO 2014039695A1
Authority
WO
WIPO (PCT)
Prior art keywords
fluid
plasma
working fluid
voltage electric
high voltage
Prior art date
Application number
PCT/US2013/058287
Other languages
French (fr)
Inventor
Geoffrey Hirson
Gus F. Shouse
Original Assignee
Powerdyne, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Powerdyne, Inc. filed Critical Powerdyne, Inc.
Priority to PCT/US2013/058287 priority Critical patent/WO2014039695A1/en
Priority to US14/426,052 priority patent/US9677431B2/en
Priority to BR112015004824A priority patent/BR112015004824A2/en
Priority to EP13836174.6A priority patent/EP2892643A4/en
Priority to KR1020157008610A priority patent/KR20150052257A/en
Publication of WO2014039695A1 publication Critical patent/WO2014039695A1/en
Priority to HK16100166.0A priority patent/HK1212282A1/en

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01KSTEAM ENGINE PLANTS; STEAM ACCUMULATORS; ENGINE PLANTS NOT OTHERWISE PROVIDED FOR; ENGINES USING SPECIAL WORKING FLUIDS OR CYCLES
    • F01K25/00Plants or engines characterised by use of special working fluids, not otherwise provided for; Plants operating in closed cycles and not otherwise provided for
    • F01K25/06Plants or engines characterised by use of special working fluids, not otherwise provided for; Plants operating in closed cycles and not otherwise provided for using mixtures of different fluids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J12/00Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor
    • B01J12/002Chemical processes in general for reacting gaseous media with gaseous media; Apparatus specially adapted therefor carried out in the plasma state
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D21/00Separation of suspended solid particles from liquids by sedimentation
    • B01D21/0009Settling tanks making use of electricity or magnetism
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D21/00Separation of suspended solid particles from liquids by sedimentation
    • B01D21/01Separation of suspended solid particles from liquids by sedimentation using flocculating agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J19/087Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy
    • B01J19/088Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09BDISPOSAL OF SOLID WASTE
    • B09B3/00Destroying solid waste or transforming solid waste into something useful or harmless
    • B09B3/20Agglomeration, binding or encapsulation of solid waste
    • B09B3/25Agglomeration, binding or encapsulation of solid waste using mineral binders or matrix
    • B09B3/29Agglomeration, binding or encapsulation of solid waste using mineral binders or matrix involving a melting or softening step
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/04Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by decomposition of inorganic compounds, e.g. ammonia
    • C01B3/042Decomposition of water
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/06Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents
    • C01B3/12Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents by reaction of water vapour with carbon monoxide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C1/00Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
    • C07C1/02Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon
    • C07C1/04Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon from oxides of a carbon from carbon monoxide with hydrogen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G2/00Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
    • C10G2/30Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
    • C10G2/32Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/04Liquid carbonaceous fuels essentially based on blends of hydrocarbons
    • C10L1/06Liquid carbonaceous fuels essentially based on blends of hydrocarbons for spark ignition
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/04Liquid carbonaceous fuels essentially based on blends of hydrocarbons
    • C10L1/08Liquid carbonaceous fuels essentially based on blends of hydrocarbons for compression ignition
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F02COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
    • F02CGAS-TURBINE PLANTS; AIR INTAKES FOR JET-PROPULSION PLANTS; CONTROLLING FUEL SUPPLY IN AIR-BREATHING JET-PROPULSION PLANTS
    • F02C1/00Gas-turbine plants characterised by the use of hot gases or unheated pressurised gases, as the working fluid
    • F02C1/04Gas-turbine plants characterised by the use of hot gases or unheated pressurised gases, as the working fluid the working fluid being heated indirectly
    • F02C1/05Gas-turbine plants characterised by the use of hot gases or unheated pressurised gases, as the working fluid the working fluid being heated indirectly characterised by the type or source of heat, e.g. using nuclear or solar energy
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05HPLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
    • H05H1/00Generating plasma; Handling plasma
    • H05H1/24Generating plasma
    • H05H1/26Plasma torches
    • H05H1/32Plasma torches using an arc
    • H05H1/34Details, e.g. electrodes, nozzles
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05HPLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
    • H05H1/00Generating plasma; Handling plasma
    • H05H1/24Generating plasma
    • H05H1/26Plasma torches
    • H05H1/32Plasma torches using an arc
    • H05H1/42Plasma torches using an arc with provisions for introducing materials into the plasma, e.g. powder, liquid
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05HPLASMA TECHNIQUE; PRODUCTION OF ACCELERATED ELECTRICALLY-CHARGED PARTICLES OR OF NEUTRONS; PRODUCTION OR ACCELERATION OF NEUTRAL MOLECULAR OR ATOMIC BEAMS
    • H05H1/00Generating plasma; Handling plasma
    • H05H1/24Generating plasma
    • H05H1/26Plasma torches
    • H05H1/32Plasma torches using an arc
    • H05H1/44Plasma torches using an arc using more than one torch
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J2219/0803Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy
    • B01J2219/0805Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges
    • B01J2219/0807Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges involving electrodes
    • B01J2219/0809Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges involving electrodes employing two or more electrodes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J2219/0803Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy
    • B01J2219/0805Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges
    • B01J2219/0807Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges involving electrodes
    • B01J2219/0815Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electric or magnetic energy giving rise to electric discharges involving electrodes involving stationary electrodes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J2219/0873Materials to be treated
    • B01J2219/0875Gas
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J2219/0873Materials to be treated
    • B01J2219/0877Liquid
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J2219/0894Processes carried out in the presence of a plasma
    • B01J2219/0898Hot plasma
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/06Integration with other chemical processes
    • C01B2203/062Hydrocarbon production, e.g. Fischer-Tropsch process
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0861Methods of heating the process for making hydrogen or synthesis gas by plasma
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00Components of fuel compositions
    • C10L2200/04Organic compounds
    • C10L2200/0407Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
    • C10L2200/0415Light distillates, e.g. LPG, naphtha
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00Components of fuel compositions
    • C10L2200/04Organic compounds
    • C10L2200/0407Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
    • C10L2200/0415Light distillates, e.g. LPG, naphtha
    • C10L2200/0423Gasoline
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00Components of fuel compositions
    • C10L2200/04Organic compounds
    • C10L2200/0407Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
    • C10L2200/043Kerosene, jet fuel
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00Components of fuel compositions
    • C10L2200/04Organic compounds
    • C10L2200/0407Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
    • C10L2200/0438Middle or heavy distillates, heating oil, gasoil, marine fuels, residua
    • C10L2200/0446Diesel
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/38Applying an electric field or inclusion of electrodes in the apparatus
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2290/00Fuel preparation or upgrading, processes or apparatus therefore, comprising specific process steps or apparatus units
    • C10L2290/42Fischer-Tropsch steps
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/36Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • Y02P20/129Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T50/00Aeronautics or air transport
    • Y02T50/60Efficient propulsion technologies, e.g. for aircraft
    • Y02T50/678Aviation using fuels of non-fossil origin

Definitions

  • Fuel materials may take on a variety of forms, from simple gasses such as hydrogen to complex mixtures including aviation fuels. Due to their wide range of chemical compositions, chemical fuels may be generated through a variety of processes and may require facilities dedicated to synthesizing only a small number of possible fuel types. Such facilities may be optimized to generate only the fuels to which they are dedicated.
  • each facility may require a specific set of precursor materials for fuel synthesis.
  • carbon-based fuels rely on thermal methods for their synthesis. Such methods may include pyrolysis, cracking, and endothermic synthesis steps. Such processes may generate excessive heat as a by-product of their synthetic methods. Further, such thermal chemistry-based synthetic methods may not be efficient even for an optimized facility.
  • a method of making a fuel fluid may include providing a first working fluid, exposing the first working fluid to a first high voltage electric field to produce a first fluid plasma, providing a second working fluid, exposing the second working fluid to a second high voltage electric field to produce a second fluid plasma, contacting the second fluid plasma with the first fluid plasma to form a fluid plasma mixture, transporting the fluid plasma mixture to a heat exchange device, cooling the fluid plasma mixture using the heat exchange device to form a fuel fluid, and collecting the fuel fluid.
  • FIG. 1A depicts a block diagram for an illustrative system and process flow for generating a fuel fluid from at least one plasma source in accordance with an
  • FIG. IB depicts a block diagram of an illustrative high- voltage electric field generator according to an embodiment.
  • FIG. 2 depicts a flow diagram of an illustrative method of making a fuel fluid using plasma sources according to an embodiment.
  • FIG. 3 depicts a flow diagram of an illustrative method of exposing a working fluid to a high- voltage electric field according to an embodiment.
  • FIG. 4 depicts a flow diagram of an illustrative method of cooling a plasma mixture according to an embodiment.
  • a "fuel” refers to any composition of matter that provides a source of energy.
  • Particular fuels that may be used herein include naphtha, diesel fuel, a diesel fuel blend, Jet Propellant 8 (JP-8) fuel, jet fuel, a jet fuel blend, or gasoline.
  • Naphtha may be a process stream that contains predominantly five carbons and heavier chemical components.
  • Naphtha may include a debutanized stream of cracked hydrocarbons that may be processed and used, for example, as a gasoline blending stock.
  • Jet fuel may be a fuel that is generally suitable for use as an aviation fuel. Jet fuel may comply with one or more regulations or requirements, such as, for example, ASTM D 1655 Specification for Aviation Turbine Fuels.
  • the jet fuel may be a liquid hydrocarbon fuel.
  • the jet fuel may include paraffins as a major component, as well as various aromatics and napthenes.
  • a blend such as the diesel fuel blend or the jet fuel blend, refers to a fuel blend that contains at least in part diesel fuel or jet fuel, respectively.
  • a "plasma torch” refers to any device capable of generating a directed flow of plasma.
  • Illustrative plasma torches may include, but are not limited to, ionized gas plasma generating systems, such as Inductively Coupled Plasma, Transferred Arc DC Plasma, and Non-Transferred Arc DC Plasma.
  • Plasma torches may be capable of reaching temperatures ranging of up to about 10,000°F to about 20,000°F (about 5,540°C to about 11,080°C), or more.
  • Each plasma torch may be a portion of a plasma reactor, which is generally a combination of a plasma torch and a reaction vessel with which the plasma torch is used.
  • the term “torch” may be used synonymously with "plasma torch.”
  • a method of making a fuel fluid may include providing a first working fluid, exposing the first working fluid to a first high voltage electric field to produce a first fluid plasma, providing a second working fluid, exposing the second working fluid to a second high voltage electric field to produce a second fluid plasma, contacting the second fluid plasma with the first fluid plasma to form a fluid plasma mixture, transporting the fluid plasma mixture to a heat exchange device, cooling the fluid plasma mixture using the heat exchange device to form a fuel fluid, and collecting the fuel fluid.
  • FIG. 1 depicts a block diagram for an illustrative system and process flow for generating a fuel fluid from at least one plasma source in accordance with an embodiment.
  • the system generally designated 100, may include one or more high- voltage electric field generators 110, 115, a processing chamber 120, a heat exchanger 125 and a fuel storage tank 130.
  • Each of the one or more high- voltage electric field generators 110, 115 may generally be any of various components that may be used to generate a high voltage potential.
  • each of the one or more high-voltage electric field generators 110, 115 may have at least one anode surface 150, at least one cathode surface 155, and an electric potential 160 between the anode surface and the cathode surface.
  • a magnetic field 165 and an electric field 170 may be generated when the electric potential 160 is applied between the at least one anode surface 150 and the at least one cathode surface 155.
  • a flow of gas may be substantially perpendicular to the magnetic field 165.
  • the flow of gas as indicated by the vertical arrow (Gas Flow B), may be substantially parallel to the magnetic field 165.
  • the magnetic field 165 and the electric field 170 may each have an effect on gas that flows through a gap between the anode surface 150 and the cathode surface 155.
  • the electric field 170 may stabilize the gas and/or ionize the gas.
  • the magnetic field 165 may alter a spin and/or a velocity of the gas.
  • each of the one or more high-voltage electric field generators 110, 115 may be a plasma torch. While FIG. 1A depicts two high-voltage electric field generators 110, 115, those skilled in the art will recognize that any number of high- voltage electric fields may be used without departing from the scope of the present disclosure. Thus, for example, the system 100 may include 1, 2, 3, 4, 5, 6, 7, 8, or more high- voltage electric fields.
  • a source of each of the one or more high- voltage electric field generators 110, 115 may be controlled by one or more control systems (not shown).
  • the one or more control systems may control all of the one or more high- voltage electric field generators 110, 115 together and may be different from or included with a control system for the entire system 100.
  • each of the one or more high- voltage electric field generators 110, 115 may have a separate control system.
  • a control system for a high-voltage electric field generator 110, 115 may include control functions for torch parameters, such as the voltage of the plasma torch and a frequency of the plasma torch.
  • Control of the high-voltage electric field generators 110, 115 may be based on one or more process measurements, including, but not limited to, a measurement of a voltage applied to components that generate the high- voltage electric field, a current drain of a voltage supply for high- voltage electric field generators, a temperature of the plasma output of the high- voltage electric field generators, and a composition of the plasma mixture in the processing chamber. It may further be appreciated that each of the high- voltage electric field generators (as illustrated by the high-voltage electric field generators 110, 115) may be controlled according to one or more process algorithms. The high-voltage electric field generators 110, 115 may be controlled according to the same process methods and/or algorithms (as provided by individual controllers or a single controller). Alternatively, each of the high- voltage electric field generators 110, 115 may be controlled according to a different process method and/or algorithm (as provided by individual controllers or by a single controller).
  • the first high voltage electric field generator 110 may be configured to receive a first working fluid
  • the second high voltage electric field generator 115 may be configured to receive a second working fluid.
  • the first working fluid may be oxygen gas
  • the second working fluid may be water vapor.
  • the processing chamber 120 as used herein may generally refer to any chamber that is capable of withstanding one or more processing conditions such as temperature, pressure, corrosion, and the like for the processes described hereinbelow.
  • the processing chamber 120 may be incorporated with the one or more high-voltage electric field generators 110, 115.
  • the processing chamber 120 may include one or more inlets for receiving plasma from the various high- voltage electric field generators 110, 115 and at least one outlet for discharging a plasma mixture, as described in greater detail herein.
  • An illustrative processing chamber 120 may be a plasma arc centrifugal treatment (PACT) system available from Retech Systems, LLC (Ukiah, CA), which includes at least one plasma torch.
  • PACT plasma arc centrifugal treatment
  • the processing chamber 120 may be maintained at a vacuum or near vacuum. In an embodiment, the processing chamber 120 may be maintained at a pressure of about 50 kPa to about 507 kPa (about 0.5 atmospheres to about 5
  • the plasma mixture while in the processing chamber 120, may attain temperatures of about 4000°C to about 6000°C, as described in greater detail herein. Higher or lower temperatures may be attained according to various conditions under which the high- voltage electric field generators 110, 115 operate.
  • the plasma mixture may be cooled within the processing chamber 120, at an exit port of the processing chamber, in a transport device (such as a pipe or other conduit) at an exit of the processing chamber, or at a combination of these locations using a coolant addition device (not shown).
  • the coolant addition device may use a coolant to effect cooling.
  • An illustrative coolant may include liquid oxygen (LOX).
  • An amount of coolant introduced into the plasma mixture by the coolant addition device may be controlled by a control system.
  • the amount of the coolant added to the plasma mixture may be controlled according to a temperature of the plasma mixture, a composition of the plasma mixture, or other measured parameters of the plasma mixture.
  • control system may be associated only with the coolant addition device. In other embodiments, the control system may be incorporated into a system for controlling the entire system 100.
  • the addition of the coolant to the plasma mixture may reduce the temperature of the resulting plasma mixture (an admixed plasma mixture) to about 1450°C to about 1650°C, including about 1450°C, about 1500°C, about 1550°C, about 1600°C, about 1650°C, or any value or range between any two of these values. It may be further appreciated that the admixed plasma mixture may have a composition that is different from that of the plasma mixture.
  • the heat exchanger 125 may generally be a device that is configured to transfer thermal energy from one medium to another such as, for example, a gas to another gas, a gas to a liquid, a liquid to another liquid, and the like.
  • Illustrative examples of the heat exchanger 125 may include a steam generating heat exchanger (i.e., a boiler), a gas-gas interchanger, a boiler feed water exchanger, a forced air exchanger, a cooling water exchanger, or a combination thereof.
  • Use of a plurality of heat exchangers 125, each producing successively lower pressure steam levels, is contemplated to be within the scope of the present disclosure.
  • the heat exchanger 125 may include a radiant heat exchanger, a convective heat exchanger, or a combination thereof. Steam and condensate may be generated from the heat exchange process and may include one or more steam products of different pressures.
  • the heat exchanger 125 may be a heat recovery steam generator (HRSG) such as, for example, a device manufactured by NEM (Leiden, Netherlands).
  • HRSG heat recovery steam generator
  • the HRSG 125 may be configured so that no loss or degradation of the plasma mixture occurs when the HRSG receives the plasma mixture from the processing chamber 120.
  • the HRSG 125 may be capable of withstanding various temperatures, pressures, corrosive chemicals, and the like when contacting the plasma mixture.
  • the HRSG 125 may be lined with a ceramic to assist in accommodating an elevated temperature of the plasma mixture.
  • the HRSG 125 may include a first inlet for receiving the plasma mixture or the admixed plasma mixture discharged from the processing chamber 120, a second inlet for receiving a fluid such as water, a first outlet for discharging steam, and a second outlet for discharging a cooled plasma mixture, as described in greater detail herein.
  • an amount of water that enters the heat exchanger 125 via the second inlet may be controlled by a control system, as described in greater detail herein.
  • a heated heat exchange material which may include steam as a non-limiting example, may exit the heat exchanger 125 by means of the first outlet. The heated heat exchange material may be further transported to a first electric turbine to generate a first supply of electric power.
  • the heat exchange material may be water, which may be converted to a supply of steam in the heat exchanger 125. Once the supply of steam has activated the electric turbine, the supply of steam may be cooled to liquid water. In some embodiments, the liquid water may be returned to the heat exchanger 125 to be reheated by more of the plasma mixture or the admixed plasma mixture. Alternatively, the first supply of steam, after activating the electric turbine, may be returned to a working fluid source to be supplied to one or more of the high-voltage electric fields 110, 115.
  • the fuel storage tank 130 is not limited by this disclosure, and may generally be any vessel configured to at least receive fuel from the heat exchanger 125.
  • the fuel storage tank 130 may, for example, be used to store fuel, transport fuel, dispense fuel, and/or the like.
  • the system 100 may further include a gas separator (not shown).
  • the gas separator may include, for example, a membrane separation system, a molecular sieve, or a combination thereof.
  • the gas separator may generally be used to separate various components described herein, and may optionally deposit the separated components into various gas holding containers.
  • the gas holding containers such as an (3 ⁇ 4 container, may each include an outflow metering device. Each outflow metering device may be controlled by a controller. Alternatively, the outflow metering devices of each of the individual gas holding containers may be controlled by the same controller.
  • Each gas holding container may also have a gas output port associated with the corresponding outflow metering device. Each gas output port may direct the gas from the corresponding gas holding container into a common supply duct.
  • the outflow metering devices of each of the gas holding containers may be controlled to permit an amount of gas into the common supply duct to create a cooled plasma mixture having a controlled composition, as described in greater detail herein.
  • the cooled plasma mixture may be controlled based on one or more gas composition sensors associated with the common supply duct.
  • the cooled mixture may be controlled based on a volume of gas emitted by the outflow metering devices of each of the individual gas holding containers.
  • the cooled plasma mixture may be controlled based on the pressure of gas contained in each of the individual gas holding containers. Accordingly, various ratios of the components of the cooled plasma mixture, as described in greater detail herein, may be obtained.
  • FIG. 2 depicts a flow diagram of an illustrative method of making a fuel fluid using plasma sources according to an embodiment.
  • the method may include providing 205 a first working fluid and providing 215 a second working fluid.
  • the first working fluid may be oxygen gas ((3 ⁇ 4) and the second working fluid may be water vapor (H 2 O).
  • the O 2 and 3 ⁇ 40 in the first processing chamber may be used as working fluids for respective plasma torches, as described herein.
  • each gas may be exposed to a high- voltage electric field.
  • the gases may be reduced to free radical species.
  • 3 ⁇ 40 may be reduced to a hydroxyl radical OH' and O 2 may be reduced to a superoxide anion radical 02' " .
  • the gases may be reduced to ionized species.
  • O 2 may be reduced to O " , 0 2 " , 0 2 + , and/or 0 + .
  • the types and amounts of reactive species created by exposure of the gases to high- voltage electric fields may differ from those generated by exposure of the gases to heat alone.
  • Each working fluid may be supplied by its own working fluid source.
  • O 2 may be supplied from an O 2 source
  • water vapor (H 2 O) may be supplied from an H 2 O source.
  • control of the fluid plasma from each of the high voltage field sources may also include control of the amount of working fluid supplied to each of the high voltage field sources.
  • the working fluid supply sources for the O 2 and H 2 O may also include control and measurement components.
  • Such components may include, without limitation, components to control the amount of the working fluid supplied by each of the working fluid supply sources (valves) and devices to measure the amount of each of the working fluid supplied (such as, for example, by measuring chemical composition or pressure of the gas delivered).
  • control systems may be specific to one or more of the working fluid supply sources.
  • all the working fluid supply sources may be controlled by the same control system.
  • the working fluid supply sources may be controlled by a control system common to the entire power generation system.
  • an embodiment may include two working fluids, illustrated by (3 ⁇ 4 and H2O, that may be combined into a combined working fluid before being supplied to a high-voltage electric field generator.
  • the O2 and the 3 ⁇ 40 may be combined into a single combined working fluid to be supplied to a high-voltage electric field generator, such as 110 (FIG. 1).
  • the controllers associated with each of the supply sources for the O2 and the 3 ⁇ 40 may cause a specific amount of each gas to be added to the combined working fluid to produce an optimized ratio of gases.
  • the controller associated with a single plasma torch may cause the plasma torch to operate under optimum conditions for a specific ratio of gases in the combined working fluid.
  • the first working fluid may be exposed 210 to a high- voltage electric field to generate a first plasma.
  • exposing 210 the first working fluid to the high- voltage electric field may include providing 305 an anode surface and providing 310 a cathode surface.
  • the anode surface and the cathode surface may be separated by a distance to create a gap between the two surfaces.
  • the distance may generally be selected such that (for the electrical voltage selected), the electrical field is about 0.3 kV/cm to about 8.0 kV/cm, including about 0.3 kV/cm, about 0.3149 kV/cm, about 0.5 kV/cm, about 0.75 kV/cm, about 1.0 kV/cm, about 1.25 kV/cm, about 1.5 kV/cm, about 1.574 kV/cm, about 2.0 kV/cm, about 2.5 kV/cm, about 3.0 kV/cm, about 3.149 kV/cm, about 3.5 kV/cm, about 4.0 kV/cm, about 4.5 kV/cm, about 5.0 kV/cm, about 5.5 kV/cm, about 6.0 kV/cm, about 6.5 kV/cm, about 7.0 kV/cm, about 7.5 kV/cm, about 7.559 k
  • Illustrative distances may be about 0.15 cm to about 0.65 cm, including about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.3175 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, or any value or range between any two of these values (including endpoints).
  • a first high voltage electric potential may be induced 315 between the anode surface and the cathode surface, and the first working fluid may be induced 320 to traverse the gap between the two surfaces.
  • the first high voltage potential may be about 2.4 kV times the gap distance in centimeters to about 60 kV times the gap distance in centimeters, including about 5 kV, about 10 kV, about 20 kV, about 30 kV, about 40 kV, about 50 kV, about 60kV, or any value or range between any two of these values (including endpoints).
  • a voltage between the anode surface and the cathode surface is 2.4 kV, thereby resulting in an electrical field of about 7.559 kV/cm.
  • the first high voltage electric potential may be an AC potential having a frequency of about 1 MHz to about 50 MHz, including about 1 MHz, about 5 MHz, about 10 MHz, about 20 MHz, about 25 MHz, about 30 MHz, about 40 MHz, about 50 MHz, or any value or range between any two of these values (including endpoints).
  • the first high- voltage electric potential may have a current of about 100 Amperes to about 1000 Amperes, including about 100 Amperes, about 200 Amperes, about 300 Amperes, about 400 Amperes, about 500 Amperes, about 600 Amperes, about 700 Amperes, about 800 Amperes, about 900 Amperes, about 1000 Amperes, or any value or range between any two of these values (including endpoints).
  • the second working fluid may be exposed 220 to a high- voltage electric field to generate a second plasma. As shown in FIG.
  • exposing 220 the second working fluid to the high- voltage electric field may include providing 305 an anode surface and providing 310 a cathode surface.
  • the anode surface and the cathode surface may be separated by a distance to create a gap between the two surfaces.
  • the distance may generally be selected such that (for the electrical voltage selected), the electrical field is about 0.3 kV/cm to about 8.0 kV/cm, including about 0.3 kV/cm, about 0.3149 kV/cm, about 0.5 kV/cm, about 0.75 kV/cm, about 1.0 kV/cm, about 1.25 kV/cm, about 1.5 kV/cm, about 1.574 kV/cm, about 2.0 kV/cm, about 2.5 kV/cm, about 3.0 kV/cm, about 3.149 kV/cm, about 3.5 kV/cm, about 4.0 kV/cm, about 4.5 kV/cm, about 5.0 kV/cm, about 5.5 kV/cm, about 6.0 kV/cm, about 6.5 kV/cm, about 7.0 kV/cm, about 7.5 kV/cm, about 7.559 k
  • Illustrative distances may be about 0.15 cm to about 0.65 cm, including about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.3175 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, or any value or range between any two of these values (including endpoints).
  • a second high voltage electric potential may be induced 315 between the anode surface and the cathode surface, and the second working fluid may be induced 320 to traverse the gap between the two surfaces.
  • the second high voltage potential may be about 2.4 kV times the gap distance in centimeters to about 60 kV times the gap distance in centimeters, including about 2.4 kV, 5 kV, about 10 kV, about 20 kV, about 30 kV, about 40 kV, about 50 kV, about 60kV, or any value or range between any two of these values (including endpoints).
  • a voltage between the anode surface and the cathode surface is 2.4 kV, thereby resulting in an electrical field of about 7.559 kV/cm.
  • the second high voltage electric potential may be an AC potential having a frequency of about 1 MHz to about 50 MHz, including about 1 MHz, about 5 MHz, about 10 MHz, about 20 MHz, about 25 MHz, about 30 MHz, about 40 MHz, about 50 MHz, or any value or range between any two of these values (including endpoints).
  • the second high- voltage electric potential may have a current of about 100 Amperes to about 1000 Amperes, including about 100 Amperes, about 200 Amperes, about 300 Amperes, about 400 Amperes, about 500 Amperes, about 600 Amperes, about 700 Amperes, about 800 Amperes, about 900 Amperes, about 1000 Amperes, or any value or range between any two of these values (including endpoints).
  • anode and cathode surfaces contacting the first working fluid and the second working fluid may be the same set of surfaces or they may be different sets of surfaces. If each working fluid contacts an independent pair of anode and cathode surfaces, the respective gap distances may be essentially the same or different, and high voltage electric potentials to which the working fluids are exposed may have essentially the same or different characteristics.
  • exposing 210 the first working fluid to a first high- voltage electric field may include causing the first working fluid to pass through a first plasma torch.
  • exposing 220 the second working fluid to a second high- voltage electric field may include causing the second working fluid to pass through a second plasma torch.
  • the first working fluid and the second working fluid may pass through the same plasma torch or may pass through separate plasma torches.
  • the first working fluid and the second working fluid may pass through a plasma torch consecutively or may pass through a plasma torch at substantially the same time.
  • exposing 210, 220 the various working fluids to various high- voltage electric fields may cause the various plasmas to reach a temperature of about 36,032°F (20,000°C).
  • the temperature may be sufficiently high to enable effective disassociation of various individual compounds in each of the various working fluids, as previously described herein.
  • the first and second plasmas may be contacted 225 in any temporal or spatial order to form a plasma mixture.
  • the first plasma and the second plasma may be contacted 225 by directing the first plasma to mix with the second plasma or directing the second plasma to mix with the first plasma, or directing the first plasma and the second plasma to mix together.
  • Contacting 225 the first plasma and the second plasma may form a plasma mixture of the two plasmas.
  • the plasma mixture may have a temperature of about 7232°F to about 10,832°F (about 4000°C to about 6000°C), including about 4000°C, about 4250°C, about 4500°C, about 4750°C, about 5000°C, about 5250°C, about 5500°C, about 5750°C, about 6000°C, or any value or range between any two of these values (including endpoints).
  • the plasma mixture may cool from the initial temperatures of the first and second plasmas upon passing through the respective high- voltage electrical fields.
  • the plasma mixture may be transported 230 to the heat exchanger.
  • Transporting 230 is not limited by this disclosure, and may be via any method of transport. Any number of pumps, conduit, channels, ducts, pipes, and/or the like may be used to transport 230 the fuel.
  • the plasma mixture may be cooled 235 to a temperature of about 100°F to about 2950°F (about 38°C to about 1620°C), including about 38°C, about 100°C, about 150°C, about 200°C, about 250°C, about 500°C, about 800°C, about 1100°C, about 1400°C, about 1600°C, about 1620°C, or any value or range between any of these values (including endpoints).
  • the plasma mixture may be cooled 235 to a temperature of about 100°F to about 400°F (about 38°C to about 204°C).
  • cooling 235 may effect a change in composition of the plasma mixture, such as dissociation of various components, as described herein.
  • the components may be separated via a gas separator and directed to various holding containers, as described in greater detail herein.
  • cooling 235 may be completed by contacting 405 the plasma mixture with a heat exchanger within a heat exchange device, such as, for example, a HRSG, to produce a cooled plasma mixture.
  • a heat exchange device such as, for example, a HRSG
  • the heat exchanged from the plasma mixture may be conveyed 410 by the heat exchange device to provide heat to a recovery steam generator, as described in greater detail herein.
  • the steam generated by the heat transfer to the recovery steam generator may provide preheated water vapor that may be used at least in part as the second working fluid for conversion into a plasma. Accordingly, the steam generated by the heat transfer may increase an efficiency of the systems and methods described herein by providing a reusable heat source.
  • the recovery steam generator may use the heat from the plasma mixture to heat and vaporize 415 a vaporizable fluid (such as liquid water or the like).
  • a vaporizable fluid such as liquid water or the like.
  • the resulting vaporized fluid (e.g., the steam) may be directed to and contacted 420 with a steam-powered electrical turbine.
  • the steam-powered electrical turbine may, in turn, generate electric power that may be used, at least in part, for providing electrical power to the system described herein and/or a facility used to generate the fuel.
  • cooling 245 the plasma mixture may include cooling with liquid oxygen ((3 ⁇ 4) to reduce the plasma mixture from a first temperature to a second temperature.
  • the first temperature as described herein, may be about 7232°F to about 10,832°F (about 4000°C to about 6000°C).
  • the second temperature as described herein, may be about 4892°F to about 5432°F (about 2700°C to about 3000°C).
  • This cooling 245 may allow for a split of (3 ⁇ 4 and 3 ⁇ 40 in the plasma mixture to become O " and 0 + , H + and OH " , and/or H " and OH + .
  • the cooling 245 may further allow for thermal chemical reconversion, thereby resulting in compounds H 2 , H 2 0, ( 3 ⁇ 4, and/or 3 ⁇ 4 ( 3 ⁇ 4.
  • the fuel may be collected 240. Collection is not limited by this disclosure, and may include any form of collection, storage, transport, dispensing, and/or the like. For example, in some embodiments, at least a portion of the fuel may be collected 240 in the fuel storage tank 130 (FIG. 1).
  • compositions, methods, and devices are described in terms of “comprising” various components or steps (interpreted as meaning “including, but not limited to”), the compositions, methods, and devices can also “consist essentially of or “consist of the various components and steps, and such terminology should be interpreted as defining essentially closed-member groups.

Abstract

Methods of making a fuel fluid are disclosed. A first working fluid and a second working fluid may be provided. The first working fluid may be exposed to a first high voltage electric field to produce a first fluid plasma, and the second working fluid may be exposed to a second high voltage electric field to produce a second fluid plasma. The first fluid plasma and the second fluid plasma may be contacted to form a fluid plasma mixture, which is transported to a heat exchange device. The fluid plasma mixture may be cooled to form a fuel fluid; and the fuel fluid may be collected.

Description

METHODS FOR GENERATING HYDROGEN GAS USING PLASMA SOURCES
CLAIM OF PRIORITY
[0001] The present application claims the benefit of and priority to U.S. Provisional Application Serial No. 61/697,148 entitled "Methods for Generating Fuel Materials and Power, and Sequestering Toxins Using Plasma Sources," which application was filed on September 5, 2012. The aforementioned application is incorporated by reference herein in its entirety and for all purposes.
BACKGROUND
[0002] Fuel materials may take on a variety of forms, from simple gasses such as hydrogen to complex mixtures including aviation fuels. Due to their wide range of chemical compositions, chemical fuels may be generated through a variety of processes and may require facilities dedicated to synthesizing only a small number of possible fuel types. Such facilities may be optimized to generate only the fuels to which they are dedicated.
Additionally, each facility may require a specific set of precursor materials for fuel synthesis.
[0003] Typically, carbon-based fuels rely on thermal methods for their synthesis. Such methods may include pyrolysis, cracking, and endothermic synthesis steps. Such processes may generate excessive heat as a by-product of their synthetic methods. Further, such thermal chemistry-based synthetic methods may not be efficient even for an optimized facility.
[0004] It is therefore desirable to develop a high efficiency method for generating gaseous and/or liquid fuel from a limited number of readily available feed stocks. Improved efficiency may be obtained in part by having the fuel generating facility also produce at least some electric power to lessen the facility's dependence on exterior power supplies. SUMMARY
[0005] In an embodiment, a method of making a fuel fluid may include providing a first working fluid, exposing the first working fluid to a first high voltage electric field to produce a first fluid plasma, providing a second working fluid, exposing the second working fluid to a second high voltage electric field to produce a second fluid plasma, contacting the second fluid plasma with the first fluid plasma to form a fluid plasma mixture, transporting the fluid plasma mixture to a heat exchange device, cooling the fluid plasma mixture using the heat exchange device to form a fuel fluid, and collecting the fuel fluid.
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] FIG. 1A depicts a block diagram for an illustrative system and process flow for generating a fuel fluid from at least one plasma source in accordance with an
embodiment.
[0007] FIG. IB depicts a block diagram of an illustrative high- voltage electric field generator according to an embodiment.
[0008] FIG. 2 depicts a flow diagram of an illustrative method of making a fuel fluid using plasma sources according to an embodiment.
[0009] FIG. 3 depicts a flow diagram of an illustrative method of exposing a working fluid to a high- voltage electric field according to an embodiment.
[0010] FIG. 4 depicts a flow diagram of an illustrative method of cooling a plasma mixture according to an embodiment.
DETAILED DESCRIPTION
[0011] This disclosure is not limited to the particular systems, devices and methods described, as these may vary. The terminology used in the description is for the purpose of describing the particular versions or embodiments only, and is not intended to limit the scope. [0012] As used in this disclosure, the singular terms "a," "an," and "the" include plural references unless the context clearly dictates otherwise. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art. Nothing in this disclosure is to be construed as an admission that the embodiments described in this disclosure are not entitled to antedate such disclosure by virtue of prior invention. As used in this disclosure, the term "comprising" means "including, but not limited to."
[0013] The following terms shall have, for the purposes of this application, the respective meanings set forth below.
[0014] A "fuel" refers to any composition of matter that provides a source of energy. Particular fuels that may be used herein include naphtha, diesel fuel, a diesel fuel blend, Jet Propellant 8 (JP-8) fuel, jet fuel, a jet fuel blend, or gasoline. Naphtha may be a process stream that contains predominantly five carbons and heavier chemical components. Naphtha may include a debutanized stream of cracked hydrocarbons that may be processed and used, for example, as a gasoline blending stock. Jet fuel may be a fuel that is generally suitable for use as an aviation fuel. Jet fuel may comply with one or more regulations or requirements, such as, for example, ASTM D 1655 Specification for Aviation Turbine Fuels. In some embodiments, the jet fuel may be a liquid hydrocarbon fuel. In some embodiments, the jet fuel may include paraffins as a major component, as well as various aromatics and napthenes. A blend, such as the diesel fuel blend or the jet fuel blend, refers to a fuel blend that contains at least in part diesel fuel or jet fuel, respectively.
[0015] A "plasma torch" refers to any device capable of generating a directed flow of plasma. Illustrative plasma torches may include, but are not limited to, ionized gas plasma generating systems, such as Inductively Coupled Plasma, Transferred Arc DC Plasma, and Non-Transferred Arc DC Plasma. Plasma torches may be capable of reaching temperatures ranging of up to about 10,000°F to about 20,000°F (about 5,540°C to about 11,080°C), or more. Each plasma torch may be a portion of a plasma reactor, which is generally a combination of a plasma torch and a reaction vessel with which the plasma torch is used. As used herein, the term "torch" may be used synonymously with "plasma torch."
[0016] In various embodiments described herein, a method of making a fuel fluid may include providing a first working fluid, exposing the first working fluid to a first high voltage electric field to produce a first fluid plasma, providing a second working fluid, exposing the second working fluid to a second high voltage electric field to produce a second fluid plasma, contacting the second fluid plasma with the first fluid plasma to form a fluid plasma mixture, transporting the fluid plasma mixture to a heat exchange device, cooling the fluid plasma mixture using the heat exchange device to form a fuel fluid, and collecting the fuel fluid.
[0017] FIG. 1 depicts a block diagram for an illustrative system and process flow for generating a fuel fluid from at least one plasma source in accordance with an embodiment. As shown in FIG. 1 , the system, generally designated 100, may include one or more high- voltage electric field generators 110, 115, a processing chamber 120, a heat exchanger 125 and a fuel storage tank 130.
[0018] Each of the one or more high- voltage electric field generators 110, 115 may generally be any of various components that may be used to generate a high voltage potential. Thus, as shown in FIG. IB, each of the one or more high-voltage electric field generators 110, 115 may have at least one anode surface 150, at least one cathode surface 155, and an electric potential 160 between the anode surface and the cathode surface. As a result, a magnetic field 165 and an electric field 170 may be generated when the electric potential 160 is applied between the at least one anode surface 150 and the at least one cathode surface 155. In some embodiments, a flow of gas, as described in greater detail herein and indicated by the horizontal arrow (Gas Flow A), may be substantially perpendicular to the magnetic field 165. In other embodiments, the flow of gas, as indicated by the vertical arrow (Gas Flow B), may be substantially parallel to the magnetic field 165. The magnetic field 165 and the electric field 170 may each have an effect on gas that flows through a gap between the anode surface 150 and the cathode surface 155. In a non-limiting example, the electric field 170 may stabilize the gas and/or ionize the gas. In another non-limiting example, the magnetic field 165 may alter a spin and/or a velocity of the gas.
[0019] Referring again to FIG. 1A, in some embodiments, each of the one or more high-voltage electric field generators 110, 115 may be a plasma torch. While FIG. 1A depicts two high-voltage electric field generators 110, 115, those skilled in the art will recognize that any number of high- voltage electric fields may be used without departing from the scope of the present disclosure. Thus, for example, the system 100 may include 1, 2, 3, 4, 5, 6, 7, 8, or more high- voltage electric fields.
[0020] It may be appreciated that a source of each of the one or more high- voltage electric field generators 110, 115 may be controlled by one or more control systems (not shown). The one or more control systems may control all of the one or more high- voltage electric field generators 110, 115 together and may be different from or included with a control system for the entire system 100. Alternatively, each of the one or more high- voltage electric field generators 110, 115 may have a separate control system. A control system for a high-voltage electric field generator 110, 115 may include control functions for torch parameters, such as the voltage of the plasma torch and a frequency of the plasma torch. Control of the high-voltage electric field generators 110, 115 may be based on one or more process measurements, including, but not limited to, a measurement of a voltage applied to components that generate the high- voltage electric field, a current drain of a voltage supply for high- voltage electric field generators, a temperature of the plasma output of the high- voltage electric field generators, and a composition of the plasma mixture in the processing chamber. It may further be appreciated that each of the high- voltage electric field generators (as illustrated by the high-voltage electric field generators 110, 115) may be controlled according to one or more process algorithms. The high-voltage electric field generators 110, 115 may be controlled according to the same process methods and/or algorithms (as provided by individual controllers or a single controller). Alternatively, each of the high- voltage electric field generators 110, 115 may be controlled according to a different process method and/or algorithm (as provided by individual controllers or by a single controller).
[0021] In operation, the first high voltage electric field generator 110 may be configured to receive a first working fluid, and the second high voltage electric field generator 115 may be configured to receive a second working fluid. In an embodiment, the first working fluid may be oxygen gas. In an embodiment, the second working fluid may be water vapor.
[0022] The processing chamber 120 as used herein may generally refer to any chamber that is capable of withstanding one or more processing conditions such as temperature, pressure, corrosion, and the like for the processes described hereinbelow. In some embodiments, the processing chamber 120 may be incorporated with the one or more high-voltage electric field generators 110, 115. In some embodiments, the processing chamber 120 may include one or more inlets for receiving plasma from the various high- voltage electric field generators 110, 115 and at least one outlet for discharging a plasma mixture, as described in greater detail herein. An illustrative processing chamber 120 may be a plasma arc centrifugal treatment (PACT) system available from Retech Systems, LLC (Ukiah, CA), which includes at least one plasma torch.
[0023] In an embodiment, the processing chamber 120 may be maintained at a vacuum or near vacuum. In an embodiment, the processing chamber 120 may be maintained at a pressure of about 50 kPa to about 507 kPa (about 0.5 atmospheres to about 5
atmospheres), including about 50 kPa, about 100 kPa, about 150 kPa, about 200 kPa, about 250 kPa, about 300 kPa, about 350 kPa, about 400 kPa, about 450 kPa, about 500 kPa, about 507 kPa, or any value or range between any two of these values (including endpoints). [0024] The plasma mixture, while in the processing chamber 120, may attain temperatures of about 4000°C to about 6000°C, as described in greater detail herein. Higher or lower temperatures may be attained according to various conditions under which the high- voltage electric field generators 110, 115 operate.
[0025] The plasma mixture may be cooled within the processing chamber 120, at an exit port of the processing chamber, in a transport device (such as a pipe or other conduit) at an exit of the processing chamber, or at a combination of these locations using a coolant addition device (not shown). In some embodiments, the coolant addition device may use a coolant to effect cooling. An illustrative coolant may include liquid oxygen (LOX). An amount of coolant introduced into the plasma mixture by the coolant addition device may be controlled by a control system. In some non-limiting examples, the amount of the coolant added to the plasma mixture may be controlled according to a temperature of the plasma mixture, a composition of the plasma mixture, or other measured parameters of the plasma mixture. In some embodiments, the control system may be associated only with the coolant addition device. In other embodiments, the control system may be incorporated into a system for controlling the entire system 100. The addition of the coolant to the plasma mixture may reduce the temperature of the resulting plasma mixture (an admixed plasma mixture) to about 1450°C to about 1650°C, including about 1450°C, about 1500°C, about 1550°C, about 1600°C, about 1650°C, or any value or range between any two of these values. It may be further appreciated that the admixed plasma mixture may have a composition that is different from that of the plasma mixture.
[0026] The heat exchanger 125 may generally be a device that is configured to transfer thermal energy from one medium to another such as, for example, a gas to another gas, a gas to a liquid, a liquid to another liquid, and the like. Illustrative examples of the heat exchanger 125 may include a steam generating heat exchanger (i.e., a boiler), a gas-gas interchanger, a boiler feed water exchanger, a forced air exchanger, a cooling water exchanger, or a combination thereof. Use of a plurality of heat exchangers 125, each producing successively lower pressure steam levels, is contemplated to be within the scope of the present disclosure. For example, the heat exchanger 125 may include a radiant heat exchanger, a convective heat exchanger, or a combination thereof. Steam and condensate may be generated from the heat exchange process and may include one or more steam products of different pressures.
[0027] In a particular embodiment, the heat exchanger 125 may be a heat recovery steam generator (HRSG) such as, for example, a device manufactured by NEM (Leiden, Netherlands). The HRSG 125 may be configured so that no loss or degradation of the plasma mixture occurs when the HRSG receives the plasma mixture from the processing chamber 120. Thus, the HRSG 125 may be capable of withstanding various temperatures, pressures, corrosive chemicals, and the like when contacting the plasma mixture. In some
embodiments, the HRSG 125 may be lined with a ceramic to assist in accommodating an elevated temperature of the plasma mixture. In some embodiments, the HRSG 125 may include a first inlet for receiving the plasma mixture or the admixed plasma mixture discharged from the processing chamber 120, a second inlet for receiving a fluid such as water, a first outlet for discharging steam, and a second outlet for discharging a cooled plasma mixture, as described in greater detail herein. In some embodiments, an amount of water that enters the heat exchanger 125 via the second inlet may be controlled by a control system, as described in greater detail herein. A heated heat exchange material, which may include steam as a non-limiting example, may exit the heat exchanger 125 by means of the first outlet. The heated heat exchange material may be further transported to a first electric turbine to generate a first supply of electric power.
[0028] In various embodiments, the heat exchange material may be water, which may be converted to a supply of steam in the heat exchanger 125. Once the supply of steam has activated the electric turbine, the supply of steam may be cooled to liquid water. In some embodiments, the liquid water may be returned to the heat exchanger 125 to be reheated by more of the plasma mixture or the admixed plasma mixture. Alternatively, the first supply of steam, after activating the electric turbine, may be returned to a working fluid source to be supplied to one or more of the high-voltage electric fields 110, 115.
[0029] The fuel storage tank 130 is not limited by this disclosure, and may generally be any vessel configured to at least receive fuel from the heat exchanger 125. In addition, the fuel storage tank 130 may, for example, be used to store fuel, transport fuel, dispense fuel, and/or the like.
[0030] In various embodiments, the system 100 may further include a gas separator (not shown). The gas separator may include, for example, a membrane separation system, a molecular sieve, or a combination thereof. The gas separator may generally be used to separate various components described herein, and may optionally deposit the separated components into various gas holding containers. The gas holding containers, such as an (¾ container, may each include an outflow metering device. Each outflow metering device may be controlled by a controller. Alternatively, the outflow metering devices of each of the individual gas holding containers may be controlled by the same controller. Each gas holding container may also have a gas output port associated with the corresponding outflow metering device. Each gas output port may direct the gas from the corresponding gas holding container into a common supply duct.
[0031] The outflow metering devices of each of the gas holding containers may be controlled to permit an amount of gas into the common supply duct to create a cooled plasma mixture having a controlled composition, as described in greater detail herein. In one non- limiting example, the cooled plasma mixture may be controlled based on one or more gas composition sensors associated with the common supply duct. In another non-limiting example, the cooled mixture may be controlled based on a volume of gas emitted by the outflow metering devices of each of the individual gas holding containers. In yet another non-limiting example, the cooled plasma mixture may be controlled based on the pressure of gas contained in each of the individual gas holding containers. Accordingly, various ratios of the components of the cooled plasma mixture, as described in greater detail herein, may be obtained.
[0032] FIG. 2 depicts a flow diagram of an illustrative method of making a fuel fluid using plasma sources according to an embodiment. As shown in FIG. 2, the method may include providing 205 a first working fluid and providing 215 a second working fluid. In one non-limiting embodiment, the first working fluid may be oxygen gas ((¾) and the second working fluid may be water vapor (H2O).
[0033] It may be appreciated that the O2 and ¾0 in the first processing chamber may be used as working fluids for respective plasma torches, as described herein. Thus, each gas may be exposed to a high- voltage electric field. As a result of such exposure, the gases may be reduced to free radical species. For example, ¾0 may be reduced to a hydroxyl radical OH' and O2 may be reduced to a superoxide anion radical 02'". In addition, the gases may be reduced to ionized species. For example, O2 may be reduced to O", 02 ", 02 +, and/or 0+. The types and amounts of reactive species created by exposure of the gases to high- voltage electric fields may differ from those generated by exposure of the gases to heat alone.
[0034] Each working fluid may be supplied by its own working fluid source. In one non- limiting example, O2 may be supplied from an O2 source, and water vapor (H2O) may be supplied from an H2O source. It may be recognized that control of the fluid plasma from each of the high voltage field sources may also include control of the amount of working fluid supplied to each of the high voltage field sources. Although not shown, it is apparent that the working fluid supply sources for the O2 and H2O, may also include control and measurement components. Such components may include, without limitation, components to control the amount of the working fluid supplied by each of the working fluid supply sources (valves) and devices to measure the amount of each of the working fluid supplied (such as, for example, by measuring chemical composition or pressure of the gas delivered). It may be further understood that such measurement and control devices may be controlled by one or more control systems, as disclosed above. In some embodiments, the control systems may be specific to one or more of the working fluid supply sources. In other embodiments, all the working fluid supply sources may be controlled by the same control system. In some embodiments, the working fluid supply sources may be controlled by a control system common to the entire power generation system.
[0035] Although not illustrated herein, an embodiment may include two working fluids, illustrated by (¾ and H2O, that may be combined into a combined working fluid before being supplied to a high-voltage electric field generator. As a non- limiting example, the O2 and the ¾0 may be combined into a single combined working fluid to be supplied to a high-voltage electric field generator, such as 110 (FIG. 1). By extension, the controllers associated with each of the supply sources for the O2 and the ¾0 may cause a specific amount of each gas to be added to the combined working fluid to produce an optimized ratio of gases. Similarly, the controller associated with a single plasma torch may cause the plasma torch to operate under optimum conditions for a specific ratio of gases in the combined working fluid.
[0036] The first working fluid may be exposed 210 to a high- voltage electric field to generate a first plasma. As shown in FIG. 3, exposing 210 the first working fluid to the high- voltage electric field may include providing 305 an anode surface and providing 310 a cathode surface. The anode surface and the cathode surface may be separated by a distance to create a gap between the two surfaces. The distance may generally be selected such that (for the electrical voltage selected), the electrical field is about 0.3 kV/cm to about 8.0 kV/cm, including about 0.3 kV/cm, about 0.3149 kV/cm, about 0.5 kV/cm, about 0.75 kV/cm, about 1.0 kV/cm, about 1.25 kV/cm, about 1.5 kV/cm, about 1.574 kV/cm, about 2.0 kV/cm, about 2.5 kV/cm, about 3.0 kV/cm, about 3.149 kV/cm, about 3.5 kV/cm, about 4.0 kV/cm, about 4.5 kV/cm, about 5.0 kV/cm, about 5.5 kV/cm, about 6.0 kV/cm, about 6.5 kV/cm, about 7.0 kV/cm, about 7.5 kV/cm, about 7.559 kV/cm, about 8.0 kV/cm, or any value or range between any two of these values (including endpoints). Illustrative distances may be about 0.15 cm to about 0.65 cm, including about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.3175 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, or any value or range between any two of these values (including endpoints).
[0037] A first high voltage electric potential may be induced 315 between the anode surface and the cathode surface, and the first working fluid may be induced 320 to traverse the gap between the two surfaces. In one non-limiting embodiment, the first high voltage potential may be about 2.4 kV times the gap distance in centimeters to about 60 kV times the gap distance in centimeters, including about 5 kV, about 10 kV, about 20 kV, about 30 kV, about 40 kV, about 50 kV, about 60kV, or any value or range between any two of these values (including endpoints). In an embodiment, a voltage between the anode surface and the cathode surface (which are separated by 0.3175 cm) is 2.4 kV, thereby resulting in an electrical field of about 7.559 kV/cm. In another non-limiting embodiment, the first high voltage electric potential may be an AC potential having a frequency of about 1 MHz to about 50 MHz, including about 1 MHz, about 5 MHz, about 10 MHz, about 20 MHz, about 25 MHz, about 30 MHz, about 40 MHz, about 50 MHz, or any value or range between any two of these values (including endpoints). In another non-limiting embodiment, the first high- voltage electric potential may have a current of about 100 Amperes to about 1000 Amperes, including about 100 Amperes, about 200 Amperes, about 300 Amperes, about 400 Amperes, about 500 Amperes, about 600 Amperes, about 700 Amperes, about 800 Amperes, about 900 Amperes, about 1000 Amperes, or any value or range between any two of these values (including endpoints). [0038] Referring back to FIG. 2, the second working fluid may be exposed 220 to a high- voltage electric field to generate a second plasma. As shown in FIG. 3, exposing 220 the second working fluid to the high- voltage electric field may include providing 305 an anode surface and providing 310 a cathode surface. The anode surface and the cathode surface may be separated by a distance to create a gap between the two surfaces. The distance may generally be selected such that (for the electrical voltage selected), the electrical field is about 0.3 kV/cm to about 8.0 kV/cm, including about 0.3 kV/cm, about 0.3149 kV/cm, about 0.5 kV/cm, about 0.75 kV/cm, about 1.0 kV/cm, about 1.25 kV/cm, about 1.5 kV/cm, about 1.574 kV/cm, about 2.0 kV/cm, about 2.5 kV/cm, about 3.0 kV/cm, about 3.149 kV/cm, about 3.5 kV/cm, about 4.0 kV/cm, about 4.5 kV/cm, about 5.0 kV/cm, about 5.5 kV/cm, about 6.0 kV/cm, about 6.5 kV/cm, about 7.0 kV/cm, about 7.5 kV/cm, about 7.559 kV/cm, about 8.0 kV/cm, or any value or range between any two of these values (including endpoints). Illustrative distances may be about 0.15 cm to about 0.65 cm, including about 0.15 cm, about 0.20 cm, about 0.25 cm, about 0.30 cm, about 0.3175 cm, about 0.35 cm, about 0.40 cm, about 0.45 cm, about 0.50 cm, about 0.55 cm, about 0.60 cm, about 0.65 cm, or any value or range between any two of these values (including endpoints).
[0039] A second high voltage electric potential may be induced 315 between the anode surface and the cathode surface, and the second working fluid may be induced 320 to traverse the gap between the two surfaces. In one non-limiting embodiment, the second high voltage potential may be about 2.4 kV times the gap distance in centimeters to about 60 kV times the gap distance in centimeters, including about 2.4 kV, 5 kV, about 10 kV, about 20 kV, about 30 kV, about 40 kV, about 50 kV, about 60kV, or any value or range between any two of these values (including endpoints). In an embodiment, a voltage between the anode surface and the cathode surface (which are separated by 0.3175 cm) is 2.4 kV, thereby resulting in an electrical field of about 7.559 kV/cm. In another non-limiting embodiment, the second high voltage electric potential may be an AC potential having a frequency of about 1 MHz to about 50 MHz, including about 1 MHz, about 5 MHz, about 10 MHz, about 20 MHz, about 25 MHz, about 30 MHz, about 40 MHz, about 50 MHz, or any value or range between any two of these values (including endpoints). In another non- limiting embodiment, the second high- voltage electric potential may have a current of about 100 Amperes to about 1000 Amperes, including about 100 Amperes, about 200 Amperes, about 300 Amperes, about 400 Amperes, about 500 Amperes, about 600 Amperes, about 700 Amperes, about 800 Amperes, about 900 Amperes, about 1000 Amperes, or any value or range between any two of these values (including endpoints).
[0040] It may be understood that the anode and cathode surfaces contacting the first working fluid and the second working fluid may be the same set of surfaces or they may be different sets of surfaces. If each working fluid contacts an independent pair of anode and cathode surfaces, the respective gap distances may be essentially the same or different, and high voltage electric potentials to which the working fluids are exposed may have essentially the same or different characteristics.
[0041] In one non-limiting example, exposing 210 the first working fluid to a first high- voltage electric field may include causing the first working fluid to pass through a first plasma torch. In another non-limiting example, exposing 220 the second working fluid to a second high- voltage electric field may include causing the second working fluid to pass through a second plasma torch. The first working fluid and the second working fluid may pass through the same plasma torch or may pass through separate plasma torches. In addition, the first working fluid and the second working fluid may pass through a plasma torch consecutively or may pass through a plasma torch at substantially the same time.
[0042] In some embodiments, exposing 210, 220 the various working fluids to various high- voltage electric fields may cause the various plasmas to reach a temperature of about 36,032°F (20,000°C). The temperature may be sufficiently high to enable effective disassociation of various individual compounds in each of the various working fluids, as previously described herein.
[0043] The first and second plasmas may be contacted 225 in any temporal or spatial order to form a plasma mixture. For example, the first plasma and the second plasma may be contacted 225 by directing the first plasma to mix with the second plasma or directing the second plasma to mix with the first plasma, or directing the first plasma and the second plasma to mix together. Contacting 225 the first plasma and the second plasma may form a plasma mixture of the two plasmas. In some non-limiting embodiments, the plasma mixture may have a temperature of about 7232°F to about 10,832°F (about 4000°C to about 6000°C), including about 4000°C, about 4250°C, about 4500°C, about 4750°C, about 5000°C, about 5250°C, about 5500°C, about 5750°C, about 6000°C, or any value or range between any two of these values (including endpoints). Thus, the plasma mixture may cool from the initial temperatures of the first and second plasmas upon passing through the respective high- voltage electrical fields.
[0044] In some embodiments, the plasma mixture may be transported 230 to the heat exchanger. Transporting 230 is not limited by this disclosure, and may be via any method of transport. Any number of pumps, conduit, channels, ducts, pipes, and/or the like may be used to transport 230 the fuel.
[0045] In various embodiments, the plasma mixture may be cooled 235 to a temperature of about 100°F to about 2950°F (about 38°C to about 1620°C), including about 38°C, about 100°C, about 150°C, about 200°C, about 250°C, about 500°C, about 800°C, about 1100°C, about 1400°C, about 1600°C, about 1620°C, or any value or range between any of these values (including endpoints). In particular embodiments, the plasma mixture may be cooled 235 to a temperature of about 100°F to about 400°F (about 38°C to about 204°C). In some embodiments, cooling 235 may effect a change in composition of the plasma mixture, such as dissociation of various components, as described herein. Thus, the components may be separated via a gas separator and directed to various holding containers, as described in greater detail herein.
[0046] In some embodiments, such as is shown in FIG. 4, cooling 235 may be completed by contacting 405 the plasma mixture with a heat exchanger within a heat exchange device, such as, for example, a HRSG, to produce a cooled plasma mixture. In some embodiments, the heat exchanged from the plasma mixture may be conveyed 410 by the heat exchange device to provide heat to a recovery steam generator, as described in greater detail herein. The steam generated by the heat transfer to the recovery steam generator may provide preheated water vapor that may be used at least in part as the second working fluid for conversion into a plasma. Accordingly, the steam generated by the heat transfer may increase an efficiency of the systems and methods described herein by providing a reusable heat source. In some embodiments, the recovery steam generator may use the heat from the plasma mixture to heat and vaporize 415 a vaporizable fluid (such as liquid water or the like). The resulting vaporized fluid (e.g., the steam) may be directed to and contacted 420 with a steam-powered electrical turbine. The steam-powered electrical turbine may, in turn, generate electric power that may be used, at least in part, for providing electrical power to the system described herein and/or a facility used to generate the fuel.
[0047] In various embodiments, cooling 245 the plasma mixture may include cooling with liquid oxygen ((¾) to reduce the plasma mixture from a first temperature to a second temperature. The first temperature, as described herein, may be about 7232°F to about 10,832°F (about 4000°C to about 6000°C). The second temperature, as described herein, may be about 4892°F to about 5432°F (about 2700°C to about 3000°C). This cooling 245 may allow for a split of (¾ and ¾0 in the plasma mixture to become O" and 0+, H+ and OH", and/or H" and OH+. The cooling 245 may further allow for thermal chemical reconversion, thereby resulting in compounds H2, H20, (¾, and/or ¾(¾. [0048] In various embodiments, the fuel may be collected 240. Collection is not limited by this disclosure, and may include any form of collection, storage, transport, dispensing, and/or the like. For example, in some embodiments, at least a portion of the fuel may be collected 240 in the fuel storage tank 130 (FIG. 1).
[0049] The present disclosure is not to be limited in terms of the particular embodiments described in this application, which are intended as illustrations of various aspects. Many modifications and variations can be made without departing from its spirit and scope, as will be apparent to those skilled in the art. Functionally equivalent methods and apparatuses within the scope of the disclosure, in addition to those enumerated in this disclosure, will be apparent to those skilled in the art from the foregoing descriptions. Such modifications and variations are intended to fall within the scope of the appended claims. The present disclosure is to be limited only by the terms of the appended claims, along with the full scope of equivalents to which such claims are entitled. It is to be understood that this disclosure is not limited to particular methods, reagents, compounds, or compositions, which can, of course, vary. It is also to be understood that the terminology used in this disclosure is for the purpose of describing particular embodiments only, and is not intended to be limiting.
[0050] With respect to the use of substantially any plural and/or singular terms in this disclosure, those having skill in the art can translate from the plural to the singular and/or from the singular to the plural as is appropriate to the context and/or application. The various singular/plural permutations may be expressly set forth in this disclosure for sake of clarity. It will be understood by those within the art that, in general, terms used in this disclosure, and especially in the appended claims (e.g. , bodies of the appended claims) are generally intended as "open" terms (e.g. , the term "including" should be interpreted as "including but not limited to," the term "having" should be interpreted as "having at least," the term "includes" should be interpreted as "includes but is not limited to," etc.). While various compositions, methods, and devices are described in terms of "comprising" various components or steps (interpreted as meaning "including, but not limited to"), the compositions, methods, and devices can also "consist essentially of or "consist of the various components and steps, and such terminology should be interpreted as defining essentially closed-member groups.
[0051] It will be further understood by those within the art that if a specific number of an introduced claim recitation is intended, such an intent will be explicitly recited in the claim, and in the absence of such recitation no such intent is present. For example, as an aid to understanding, the following appended claims may contain usage of the introductory phrases "at least one" and "one or more" to introduce claim recitations. However, the use of such phrases should not be construed to imply that the introduction of a claim recitation by the indefinite articles "a" or "an" limits any particular claim containing such introduced claim recitation to embodiments containing only one such recitation, even when the same claim includes the introductory phrases "one or more" or "at least one" and indefinite articles such as "a" or "an" (e.g. , "a" and/or "an" should be interpreted to mean "at least one" or "one or more"); the same holds true for the use of definite articles used to introduce claim recitations. In addition, even if a specific number of an introduced claim recitation is explicitly recited, those skilled in the art will recognize that such recitation should be interpreted to mean at least the recited number (e.g. , the bare recitation of "two recitations," without other modifiers, means at least two recitations, or two or more recitations). Furthermore, in those instances where a convention analogous to "at least one of A, B, and C, etc." is used, in general such a construction is intended in the sense one having skill in the art would understand the convention (e.g. , " a system having at least one of A, B, and C" would include but not be limited to systems that have A alone, B alone, C alone, A and B together, A and C together, B and C together, and/or A, B, and C together, etc.). It will be further understood by those within the art that virtually any disjunctive word and/or phrase presenting two or more alternative terms, whether in the description, claims, or drawings, should be understood to contemplate the possibilities of including one of the terms, either of the terms, or both terms. For example, the phrase "A or B" will be understood to include the possibilities of "A" or "B" or "A and B."
[0052] As will be understood by one skilled in the art, for any and all purposes, such as in terms of providing a written description, all ranges disclosed in this disclosure also encompass any and all possible subranges and combinations of subranges thereof. Any listed range can be easily recognized as sufficiently describing and enabling the same range being broken down into at least equal halves, thirds, quarters, fifths, tenths, etc. As a non-limiting example, each range discussed in this disclosure can be readily broken down into a lower third, middle third and upper third, etc. As will also be understood by one skilled in the art all language such as "up to," "at least," and the like include the number recited and refer to ranges which can be subsequently broken down into subranges as discussed above. Finally, as will be understood by one skilled in the art, a range includes each individual member.
[0053] From the foregoing, it will be appreciated that various embodiments of the present disclosure have been described for purposes of illustration, and that various modifications may be made without departing from the scope and spirit of the present disclosure. Accordingly, the various embodiments disclosed are not intended to be limiting, with the true scope and spirit being indicated by the following claims.

Claims

CLAIMS What Is Claimed Is:
1. A method of making a fuel fluid, the method comprising:
providing a first working fluid;
exposing the first working fluid to a first high voltage electric field to produce a first fluid plasma;
providing a second working fluid;
exposing the second working fluid to a second high voltage electric field to produce a second fluid plasma;
contacting the second fluid plasma with the first fluid plasma to form a fluid plasma mixture;
transporting the fluid plasma mixture to a heat exchange device;
cooling the fluid plasma mixture using the heat exchange device to form a fuel fluid; and
collecting the fuel fluid.
2. The method of claim 1, wherein the first working fluid is oxygen gas.
3. The method of claim 1, wherein the second working fluid is water vapor.
4. The method of claim 1, wherein exposing the first working fluid to a first high voltage electric field comprises:
providing an anode surface;
providing a cathode surface at a distance from the anode surface to create a gap between the anode surface and the cathode surface; providing a high voltage electric potential between the anode surface and the cathode surface; and
causing the first working fluid to traverse the gap.
5. The method of claim 4, wherein the high voltage electric potential is about 5 kV/cm times the distance in centimeters to about 60 kV/cm times the distance in centimeters.
6. The method of claim 4, wherein the first high voltage electric potential has a frequency of about 1 MHz to about 50 MHz.
7. The method of claim 1, wherein exposing the second working fluid to a second high voltage electric field comprises:
providing an anode surface;
providing a cathode surface at a distance from the anode surface to create a gap between the anode surface and the cathode surface;
providing a high voltage electric potential between the anode surface and the cathode surface; and
causing the second working fluid to traverse the gap.
8. The method of claim 7, wherein the high voltage electric potential is about 2.4 kV times the distance in centimeters to about 60 kV times the distance in centimeters.
9. The method of claim 7, wherein the second high voltage electric potential has a frequency of about 1 MHz to about 50 MHz.
10. The method of claim 1, wherein exposing the first working fluid to a first high voltage electric field comprises causing the first working fluid to pass through a first plasma torch.
11. The method of claim 1, wherein exposing the second working fluid to a second high voltage electric field comprises causing the second working fluid to pass through a second plasma torch.
12. The method of claim 1, wherein:
exposing the first working fluid to a first high voltage electric field comprises causing the first working fluid to pass through a plasma torch, and
exposing the second working fluid to a second high voltage electric field comprises causing the second working fluid to pass through the plasma torch.
13. The method of claim 1, wherein contacting the second fluid plasma with the first fluid plasma comprises directing the second fluid plasma to mix with the first fluid plasma, directing the first fluid plasma to mix with the second fluid plasma, or directing the second fluid plasma and directing the first fluid plasma to mix together.
14. The method of claim 1, wherein the fluid plasma mixture has an initial temperature of about 7232 °F (4000°C) to about 36032°F (20000°C).
15. The method of claim 1, further comprising:
cooling the plasma mixture using a coolant prior to transporting the plasma mixture to the heat exchange device.
16. The method of claim 15, wherein the coolant comprises liquid oxygen.
17. The method of claim 1, wherein cooling the fluid plasma mixture comprises cooling the fluid plasma mixture to a temperature of about 100 °F (38 °C) to about 2950 °F
(1620 °C).
18. The method of claim 1, wherein the heat exchange device is a heat recovery steam generator.
19. The method of claim 18, wherein the second working fluid comprises at least in part an amount of steam generated by the heat recovery steam generator.
20. The method of claim 1 , wherein the fuel fluid is hydrogen.
PCT/US2013/058287 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources WO2014039695A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
PCT/US2013/058287 WO2014039695A1 (en) 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources
US14/426,052 US9677431B2 (en) 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources
BR112015004824A BR112015004824A2 (en) 2012-09-05 2013-09-05 method to produce a combustible fluid
EP13836174.6A EP2892643A4 (en) 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources
KR1020157008610A KR20150052257A (en) 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources
HK16100166.0A HK1212282A1 (en) 2012-09-05 2016-01-08 Methods for generating hydrogen gas using plasma sources

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261697148P 2012-09-05 2012-09-05
US61/697,148 2012-09-05
PCT/US2013/058287 WO2014039695A1 (en) 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources

Publications (1)

Publication Number Publication Date
WO2014039695A1 true WO2014039695A1 (en) 2014-03-13

Family

ID=55538127

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2013/058287 WO2014039695A1 (en) 2012-09-05 2013-09-05 Methods for generating hydrogen gas using plasma sources

Country Status (6)

Country Link
US (1) US9677431B2 (en)
EP (1) EP2892643A4 (en)
KR (1) KR20150052257A (en)
BR (1) BR112015004824A2 (en)
HK (1) HK1212282A1 (en)
WO (1) WO2014039695A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2893325A4 (en) 2012-09-05 2016-05-18 Powerdyne Inc Fuel generation using high-voltage electric fields methods
KR102252636B1 (en) * 2019-05-14 2021-05-18 주식회사 에이아이코리아 Hydrogen purification system
KR102262103B1 (en) * 2019-05-14 2021-06-09 주식회사 에이아이코리아 Reformer system including plasma apparatus

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2379892A1 (en) * 1999-07-29 2001-02-08 David Systems & Technology S.L. Plasma converter of fossil fuels into hydrogen-rich gas
US6372156B1 (en) * 1999-08-19 2002-04-16 Bechtel Bwxt Idaho, Llc Methods of chemically converting first materials to second materials utilizing hybrid-plasma systems
US20060233699A1 (en) * 2003-04-15 2006-10-19 Mills Randell L Plasma reactor and process for producing lower-energy hydrogen species
US20080083701A1 (en) * 2006-10-04 2008-04-10 Mks Instruments, Inc. Oxygen conditioning of plasma vessels
US7384619B2 (en) * 2003-06-30 2008-06-10 Bar-Gadda, Llc Method for generating hydrogen from water or steam in a plasma
WO2009156761A2 (en) * 2008-06-25 2009-12-30 Horizon Ventures Limited Processing of waste
US20110265698A1 (en) * 2010-05-03 2011-11-03 Powerdyne, Inc. System and method for reutilizing co2 from combusted carbonaceous material

Family Cites Families (123)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1746464A (en) 1925-07-21 1930-02-11 Fischer Franz Process for the production of paraffin-hydrocarbons with more than one carbon atom
GB573982A (en) 1941-01-14 1945-12-17 Synthetic Oils Ltd Improvements in or relating to methods of producing hydrocarbon oils from gaseous mixtures of hydrogen and carbon monoxide
US3979205A (en) 1971-04-07 1976-09-07 Wanzenberg Fritz Walter Metal recovery method
SE434163B (en) 1981-03-10 1984-07-09 Skf Steel Eng Ab SET AND DEVICE FOR PREPARING A MAIN COOLOXIDE AND VETGAN CONTAINING GAS FROM COAL AND / OR CARBON-CONTAINING INGREDIENTS
SE451033B (en) 1982-01-18 1987-08-24 Skf Steel Eng Ab SET AND DEVICE FOR CONVERSION OF WASTE MATERIALS WITH PLASMA MAGAZINE
GB8405381D0 (en) 1984-03-01 1984-04-04 Shell Int Research Catalytic treatment of hydrocarbon oils
FR2610087B1 (en) 1987-01-22 1989-11-24 Aerospatiale PROCESS AND DEVICE FOR THE DESTRUCTION OF SOLID WASTE BY PYROLYSIS
YU46333B (en) 1987-04-30 1993-05-28 Oy Partek Ab MELTING OVEN
US5136137A (en) 1987-05-04 1992-08-04 Retech, Inc. Apparatus for high temperature disposal of hazardous waste materials
US4770109A (en) 1987-05-04 1988-09-13 Retech, Inc. Apparatus and method for high temperature disposal of hazardous waste materials
DK158382C (en) 1987-10-15 1990-10-22 Rockwool Int PROCEDURE FOR PREPARING A MELT FOR THE FORMATION OF MINERAL WOOL AND APPARATUS FOR EXERCISING THE PROCEDURE
US4845334A (en) 1988-01-26 1989-07-04 Oregon Metallurgical Corporation Plasma furnace inert gas recycling system and process
US4898748A (en) 1988-08-31 1990-02-06 The Board Of Trustees Of Leland Stanford Junior University Method for enhancing chemical reactivity in thermal plasma processes
US5138959A (en) 1988-09-15 1992-08-18 Prabhakar Kulkarni Method for treatment of hazardous waste in absence of oxygen
US5319176A (en) 1991-01-24 1994-06-07 Ritchie G. Studer Plasma arc decomposition of hazardous wastes into vitrified solids and non-hazardous gasses
US5288969A (en) 1991-08-16 1994-02-22 Regents Of The University Of California Electrodeless plasma torch apparatus and methods for the dissociation of hazardous waste
US5725616A (en) 1991-12-12 1998-03-10 Kvaerner Engineering A.S. Method for combustion of hydrocarbons
JP3284606B2 (en) 1992-09-24 2002-05-20 石川島播磨重工業株式会社 Ash melting furnace
US5301620A (en) 1993-04-01 1994-04-12 Molten Metal Technology, Inc. Reactor and method for disassociating waste
US5534659A (en) 1994-04-18 1996-07-09 Plasma Energy Applied Technology Incorporated Apparatus and method for treating hazardous waste
US5611947A (en) 1994-09-07 1997-03-18 Alliant Techsystems, Inc. Induction steam plasma torch for generating a steam plasma for treating a feed slurry
US5798496A (en) 1995-01-09 1998-08-25 Eckhoff; Paul S. Plasma-based waste disposal system
US5666891A (en) 1995-02-02 1997-09-16 Battelle Memorial Institute ARC plasma-melter electro conversion system for waste treatment and resource recovery
US6018471A (en) 1995-02-02 2000-01-25 Integrated Environmental Technologies Methods and apparatus for treating waste
US5798497A (en) 1995-02-02 1998-08-25 Battelle Memorial Institute Tunable, self-powered integrated arc plasma-melter vitrification system for waste treatment and resource recovery
US6821500B2 (en) 1995-03-14 2004-11-23 Bechtel Bwxt Idaho, Llc Thermal synthesis apparatus and process
US5749937A (en) 1995-03-14 1998-05-12 Lockheed Idaho Technologies Company Fast quench reactor and method
US7576296B2 (en) 1995-03-14 2009-08-18 Battelle Energy Alliance, Llc Thermal synthesis apparatus
US6187226B1 (en) 1995-03-14 2001-02-13 Bechtel Bwxt Idaho, Llc Thermal device and method for production of carbon monoxide and hydrogen by thermal dissociation of hydrocarbon gases
US5673635A (en) 1995-06-12 1997-10-07 L.E. Maxwitat Process for the recycling of organic wastes
US5544597A (en) 1995-08-29 1996-08-13 Plasma Technology Corporation Plasma pyrolysis and vitrification of municipal waste
US6355904B1 (en) 1996-06-07 2002-03-12 Science Applications International Corporation Method and system for high-temperature waste treatment
US5868027A (en) 1996-09-30 1999-02-09 Mississippi State University Measurement of viscosity of a melt in a plasma centrifugal furnace
US7338563B2 (en) 1996-10-16 2008-03-04 Clark Steve L Process for cleaning hydrocarbons from soils
CA2188357C (en) 1996-10-21 1999-09-07 Peter G. Tsantrizos plasma gasification and vitrification of ashes
US6602920B2 (en) 1998-11-25 2003-08-05 The Texas A&M University System Method for converting natural gas to liquid hydrocarbons
US6153852A (en) * 1999-02-12 2000-11-28 Thermal Conversion Corp Use of a chemically reactive plasma for thermal-chemical processes
EP1038942A1 (en) 1999-03-24 2000-09-27 Abb Research Ltd. Fuel synthesis process by dielectric barrier discharge of a gaseous composition, fuel thus obtained and apparatus therefore
US6173002B1 (en) 1999-04-21 2001-01-09 Edgar J. Robert Electric arc gasifier as a waste processor
SE516722C2 (en) 1999-04-28 2002-02-19 Hana Barankova Process and apparatus for plasma gas treatment
US6552295B2 (en) 1999-12-20 2003-04-22 Research Triangle Institute Plasma furnace disposal of hazardous wastes
WO2001046067A1 (en) 1999-12-21 2001-06-28 Bechtel Bwxt Idaho, Llc Hydrogen and elemental carbon production from natural gas and other hydrocarbons
US6289851B1 (en) 2000-10-18 2001-09-18 Institute Of Gas Technology Compact low-nox high-efficiency heating apparatus
JP4756739B2 (en) 2000-12-28 2011-08-24 株式会社筑波バイオテック研究所 Water purification equipment containing dissolved organic substances and trace amounts of harmful substances
US6685754B2 (en) 2001-03-06 2004-02-03 Alchemix Corporation Method for the production of hydrogen-containing gaseous mixtures
EP1270508B1 (en) 2001-06-26 2007-01-03 H2 Tec Ag Process and device for producing hydrogen
US7622693B2 (en) 2001-07-16 2009-11-24 Foret Plasma Labs, Llc Plasma whirl reactor apparatus and methods of use
US6987792B2 (en) 2001-08-22 2006-01-17 Solena Group, Inc. Plasma pyrolysis, gasification and vitrification of organic material
US6976362B2 (en) 2001-09-25 2005-12-20 Rentech, Inc. Integrated Fischer-Tropsch and power production plant with low CO2 emissions
CA2357527C (en) 2001-10-01 2009-12-01 Technology Convergence Inc. Methanol recycle stream
US6505567B1 (en) 2001-11-26 2003-01-14 Alstom (Switzerland) Ltd Oxygen fired circulating fluidized bed steam generator
AUPS220302A0 (en) 2002-05-08 2002-06-06 Chang, Chak Man Thomas A plasma formed within bubbles in an aqueous medium and uses therefore
RU2286837C2 (en) 2002-05-08 2006-11-10 ЛАУ Эдмунд Кин Он Method and device for treating harmful waste
CA2424805C (en) 2003-04-04 2009-05-26 Pyrogenesis Inc. Two-stage plasma process for converting waste into fuel gas and apparatus therefor
US6874434B1 (en) 2003-04-18 2005-04-05 Bigelow Aerospace Biomass waste disposal method and apparatus
WO2004112447A2 (en) * 2003-06-11 2004-12-23 Nuvotec, Inc. Inductively coupled plasma/partial oxidation reformation of carbonaceous compounds to produce fuel for energy production
CA2572434A1 (en) 2003-06-30 2005-01-20 Bar-Gadda, Llc. Dissociation of molecular water into molecular hydrogen
US7183451B2 (en) 2003-09-23 2007-02-27 Synfuels International, Inc. Process for the conversion of natural gas to hydrocarbon liquids
US7070634B1 (en) 2003-11-03 2006-07-04 Wang Chi S Plasma reformer for hydrogen production from water and fuel
US7452392B2 (en) 2003-11-29 2008-11-18 Nick Peter A Process for pyrolytic heat recovery enhanced with gasification of organic material
US7028478B2 (en) 2003-12-16 2006-04-18 Advanced Combustion Energy Systems, Inc. Method and apparatus for the production of energy
FR2866414B1 (en) 2004-02-18 2006-03-17 Commissariat Energie Atomique DEVICE AND METHOD FOR DESTRUCTION OF LIQUID, PULVERULENT OR GASEOUS WASTE BY INDUCTIVE PLASMA
US6971323B2 (en) 2004-03-19 2005-12-06 Peat International, Inc. Method and apparatus for treating waste
US7024800B2 (en) 2004-07-19 2006-04-11 Earthrenew, Inc. Process and system for drying and heat treating materials
US7216484B2 (en) 2005-03-11 2007-05-15 Villalobos Victor M Arc-hydrolysis steam generator apparatus and method
DE102005021500A1 (en) 2005-05-10 2006-11-16 Uhde Gmbh Process for heating a steam / natural gas mixture in the region of a gas collecting pipe after a primary reformer
EP1896553A4 (en) 2005-06-03 2010-09-01 Plascoenergy Ip Holdings Slb A system for the conversion of carbonaceous feedstocks to a gas of a specified composition
US20080222956A1 (en) 2005-06-03 2008-09-18 Plasco Energy Group Inc. System for the Conversion of Coal to a Gas of Specified Composition
US20070017228A1 (en) 2005-07-06 2007-01-25 Integrated Environmental Technologies, Llc Method for enhancing the efficient operation of electrical power plants and energy storage
GB0516695D0 (en) 2005-08-15 2005-09-21 Boc Group Plc Microwave plasma reactor
CN1810938A (en) 2005-08-24 2006-08-02 周开根 Method of synthesizing fuel gas with water and oil and its burner
FR2892127B1 (en) 2005-10-14 2012-10-19 Commissariat Energie Atomique DEVICE FOR GASIFYING BIOMASS AND ORGANIC WASTE AT HIGH TEMPERATURE AND WITH EXTERNAL ENERGY DELIVERY FOR THE GENERATION OF A HIGH-QUALITY SYNTHESIS GAS
GB0521830D0 (en) 2005-10-26 2005-12-07 Boc Group Plc Plasma reactor
US7736400B2 (en) 2006-02-14 2010-06-15 Gas Technology Institute Plasma assisted conversion of carbonaceous materials into a gas
US7832344B2 (en) 2006-02-28 2010-11-16 Peat International, Inc. Method and apparatus of treating waste
US8216433B2 (en) 2006-03-07 2012-07-10 University Of The Ryukyus Plasma generator and method of generating plasma using the same
KR100807806B1 (en) 2006-04-04 2008-02-27 제주대학교 산학협력단 DC arc plasmatron and the method using the same
WO2008008104A2 (en) 2006-04-05 2008-01-17 Foret Plasma Labs, Llc System, method and apparatus for treating liquids with wave energy from plasma
US20070267289A1 (en) 2006-04-06 2007-11-22 Harry Jabs Hydrogen production using plasma- based reformation
EP2019981A4 (en) 2006-05-05 2010-04-21 Plascoenergy Ip Holdings Slb A control system for the conversion of a carbonaceous feedstock into gas
EP2043951A4 (en) 2006-05-05 2010-04-14 Plascoenergy Ip Holdings Slb A gas reformulating system using plasma torch heat
US20070258869A1 (en) * 2006-05-05 2007-11-08 Andreas Tsangaris Residue Conditioning System
NZ573217A (en) 2006-05-05 2011-11-25 Plascoenergy Ip Holdings S L Bilbao Schaffhausen Branch A facility for conversion of carbonaceous feedstock into a reformulated syngas containing CO and H2
DE102006035893A1 (en) 2006-07-31 2008-02-07 Wolf, Bodo M., Dr. Process for the reprocessing of combustion products of fossil fuels
FR2904830B1 (en) 2006-08-08 2012-10-19 Inst Francais Du Petrole PROCESS FOR PRODUCTION OF SYNTHESIS GAS WITH PARTIAL OXIDATION AND VAPOREFORMING
US7833296B2 (en) 2006-10-02 2010-11-16 Clark Steve L Reduced-emission gasification and oxidation of hydrocarbon materials for power generation
US20080223047A1 (en) 2006-10-19 2008-09-18 Troy Lee Oliver Xplogen TM: a system, method, and apparatus for generating energy from a series of dissociation reactions
CA2666959C (en) 2006-10-20 2015-06-23 Shell Internationale Research Maatschappij B.V. Moving hydrocarbons through portions of tar sands formations with a fluid
US20090049748A1 (en) 2007-01-04 2009-02-26 Eric Day Method and system for converting waste into energy
AU2007351914A1 (en) 2007-04-18 2008-10-30 Sgc Energia Sgps, S.A. Waste to liquid hydrocarbon refinery system
US8277631B2 (en) 2007-05-04 2012-10-02 Principle Energy Solutions, Inc. Methods and devices for the production of hydrocarbons from carbon and hydrogen sources
US8268094B2 (en) 2007-05-09 2012-09-18 Air Products And Chemicals, Inc. Furnace atmosphere activation method and apparatus
PA8780401A1 (en) 2007-05-11 2008-12-18 Plasco Energy Group Inc "A GAS REFORMULATION SYSTEM UNDERSTANDING MEANS TO OPTIMIZE THE EFFECTIVENESS OF GAS CONVERSION"
MX356141B (en) 2007-07-06 2018-05-16 Evaco Llc Carbon free dissociation of water and production of hydrogen related power.
US8367005B2 (en) 2007-07-12 2013-02-05 Imagineering, Inc. Gas processing apparatus, gas processing system, and gas processing method, and exhaust gas processing system and internal combustion engine using the same
KR100898813B1 (en) 2007-10-11 2009-05-22 문 기 조 Plasma decomposition apparatus and method for carbon dioxide
US8199790B2 (en) 2007-11-02 2012-06-12 Plasma Waste Recycling, Inc. Reactor vessel for plasma gasification
US20090133407A1 (en) 2007-11-28 2009-05-28 Nrg Energy, Inc. Plasma gasification system
US8845772B2 (en) 2008-01-23 2014-09-30 Peter J. Schubert Process and system for syngas production from biomass materials
US8303916B2 (en) 2008-02-01 2012-11-06 Oscura, Inc. Gaseous transfer in multiple metal bath reactors
EP2247347A4 (en) 2008-02-08 2013-08-14 Peat International Inc Method and apparatus of treating waste
EP2253009B1 (en) 2008-02-12 2019-08-28 Purdue Research Foundation Low temperature plasma probe and methods of use thereof
WO2010014938A2 (en) 2008-07-31 2010-02-04 Alstom Technology Ltd. System for hot solids combustion and gasification
IT1391148B1 (en) 2008-08-06 2011-11-18 Reco 2 S R L METHOD AND APPARATUS FOR PURIFYING GAS
US7674443B1 (en) 2008-08-18 2010-03-09 Irvin Davis Zero emission gasification, power generation, carbon oxides management and metallurgical reduction processes, apparatus, systems, and integration thereof
WO2010056462A1 (en) 2008-11-12 2010-05-20 Uni-Control, Llc Biological water-gas shift reaction system comprising plasma gasification
GB2466664B (en) 2009-01-06 2015-04-01 Perlemax Ltd Plasma microreactor apparatus, sterilisation unit and analyser
US20110067376A1 (en) 2009-03-16 2011-03-24 Geovada, Llc Plasma-based waste-to-energy techniques
US20100229522A1 (en) 2009-03-16 2010-09-16 Jim Kingzett Plasma-Assisted E-Waste Conversion Techniques
MY151894A (en) 2009-07-17 2014-07-14 Green Energy And Technology Sdn Bhd Advanced thermal reactor
PT2848777T (en) 2010-01-21 2016-12-28 Powerdyne Inc Generating steam from carbonaceous material
EP2534122A4 (en) 2010-02-08 2013-12-18 Fulcrum Bioenergy Inc Processes for economically converting municipal solid waste into ethanol
CN102906227A (en) 2010-02-13 2013-01-30 麦卡利斯特技术有限责任公司 Carbon-based durable goods and renewable fuel from biomass waste dissociation
GB2482263B8 (en) 2010-03-01 2012-11-14 Plascoenergy Ip Holdings S L Carbon conversion system with integrated processing zones
CA2803896A1 (en) 2010-07-01 2012-01-05 Aarmonia Chemicals Private, Ltd. Diesel fuel additive
US9045337B2 (en) 2010-08-09 2015-06-02 Lai O. Kuku Waste material, coal, used tires and biomass conversion to alternative energy and synthetic fuels solutions system with carbon capture and liquefaction
CA2813062C (en) 2010-09-24 2018-10-30 James Charles Juranitch Renewable combined cycle low turbine boost
US20120090985A1 (en) 2010-10-01 2012-04-19 Drexel University Non-equilibrium gliding arc plasma system for co2 dissociation
KR20140138328A (en) 2010-11-05 2014-12-03 비코 에이엘디 인코포레이티드 Radical reactor with multiple plasma chambers
EP2638130B1 (en) 2010-11-10 2018-06-06 Air Products and Chemicals, Inc. Method for forming a syngas stream
CN103249812A (en) 2010-12-08 2013-08-14 丰田自动车株式会社 Fuel production system
EP2710235B1 (en) 2011-05-16 2015-07-15 Powerdyne, Inc. Steam generation system
US20140239232A1 (en) 2011-06-21 2014-08-28 Vernon Eric Staton Apparatus and method for hydrocarbon pyrolysis

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2379892A1 (en) * 1999-07-29 2001-02-08 David Systems & Technology S.L. Plasma converter of fossil fuels into hydrogen-rich gas
US6372156B1 (en) * 1999-08-19 2002-04-16 Bechtel Bwxt Idaho, Llc Methods of chemically converting first materials to second materials utilizing hybrid-plasma systems
US20060233699A1 (en) * 2003-04-15 2006-10-19 Mills Randell L Plasma reactor and process for producing lower-energy hydrogen species
US7384619B2 (en) * 2003-06-30 2008-06-10 Bar-Gadda, Llc Method for generating hydrogen from water or steam in a plasma
US20080083701A1 (en) * 2006-10-04 2008-04-10 Mks Instruments, Inc. Oxygen conditioning of plasma vessels
WO2009156761A2 (en) * 2008-06-25 2009-12-30 Horizon Ventures Limited Processing of waste
US20110265698A1 (en) * 2010-05-03 2011-11-03 Powerdyne, Inc. System and method for reutilizing co2 from combusted carbonaceous material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2892643A4 *

Also Published As

Publication number Publication date
HK1212282A1 (en) 2016-06-10
US9677431B2 (en) 2017-06-13
EP2892643A4 (en) 2016-05-11
BR112015004824A2 (en) 2017-07-04
KR20150052257A (en) 2015-05-13
US20150224467A1 (en) 2015-08-13
EP2892643A1 (en) 2015-07-15

Similar Documents

Publication Publication Date Title
US8784617B2 (en) Process of converting gaseous hydrocarbons to a liquid hydrocarbon composition
Czylkowski et al. Microwave plasma-based method of hydrogen production via combined steam reforming of methane
Sun et al. Large capacity hydrogen production by microwave discharge plasma in liquid fuels ethanol
HRP20211476T1 (en) An apparatus, a system and a method for producing hydrogen
RU2585647C2 (en) Method of modifying a methane-containing gas stream
Czylkowski et al. Hydrogen production by conversion of ethanol using atmospheric pressure microwave plasmas
US9677431B2 (en) Methods for generating hydrogen gas using plasma sources
Chernyak et al. Plasma-assisted reforming of ethanol in dynamic plasma-liquid system: experiments and modeling
KR101581261B1 (en) Methods for power generation from h2o, co2, o2 and a carbon feed stock
KR101581263B1 (en) System for generating fuel materials using fischer-tropsch catalysts and plasma sources
US9410452B2 (en) Fuel generation using high-voltage electric fields methods
US9382818B2 (en) Fuel generation using high-voltage electric fields methods
US9765270B2 (en) Fuel generation using high-voltage electric fields methods
El‐Shafie et al. Comprehensive assessment of hydrogen production in argon‐water vapors plasmolysis
Snoeckx et al. A combined study for turning CO $ _2 $ and H $ _2 $ O into value-added products in a dielectric barrier discharge
KR101369739B1 (en) Metal organic deposition plasma chamber having multi plasma discharging tube
CN111366492A (en) System and method for determining optimal value of water adsorption amount of unit photocatalyst in photocatalytic reaction
OA10872A (en) Conversion of hydrocarbons assisted by gliding electric arcs

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: 13836174

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 14426052

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: P297/2015

Country of ref document: AE

ENP Entry into the national phase

Ref document number: 20157008610

Country of ref document: KR

Kind code of ref document: A

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112015004824

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112015004824

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20150304