US20080308427A1 - System and process for producing alcohol - Google Patents

System and process for producing alcohol Download PDF

Info

Publication number
US20080308427A1
US20080308427A1 US12/140,864 US14086408A US2008308427A1 US 20080308427 A1 US20080308427 A1 US 20080308427A1 US 14086408 A US14086408 A US 14086408A US 2008308427 A1 US2008308427 A1 US 2008308427A1
Authority
US
United States
Prior art keywords
liquid mixture
electrochemically
electrolysis cell
alcohol
water
Prior art date
Legal status (The legal status 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 status listed.)
Abandoned
Application number
US12/140,864
Other languages
English (en)
Inventor
Bruce F. Field
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tennant Co
Original Assignee
Tennant Co
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 Tennant Co filed Critical Tennant Co
Priority to US12/140,864 priority Critical patent/US20080308427A1/en
Assigned to TENNANT COMPANY reassignment TENNANT COMPANY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: FIELD, BRUCE F.
Publication of US20080308427A1 publication Critical patent/US20080308427A1/en
Assigned to JPMORGAN CHASE BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT reassignment JPMORGAN CHASE BANK, NATIONAL ASSOCIATION, AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: TENNANT COMPANY
Assigned to TENNANT COMPANY reassignment TENNANT COMPANY RELEASE BY SECURED PARTY (SEE DOCUMENT FOR DETAILS). Assignors: JPMORGAN CHASE BANK, NATIONAL ASSOCIATION
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/06—Ethanol, i.e. non-beverage
    • C12P7/08—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate
    • C12P7/10—Ethanol, i.e. non-beverage produced as by-product or from waste or cellulosic material substrate substrate containing cellulosic material
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/06—Ethanol, i.e. non-beverage
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel

Definitions

  • the present disclosure relates to systems and processes for producing alcohols. More specifically, the present disclosure relates to alcohol production using electrochemically-activated water.
  • Alcohols such as ethyl alcohol
  • Wet milling processes involve separating feedstock into components parts, such as starch, prior to undergoing a fermentation process to produce the alcohol.
  • dry milling processes involve grinding the feedstock into fine powder granules, and the starch in the granules is then converted to alcohol during the fermentation process.
  • Agricultural feedstock products of many kinds can be made into alcohol.
  • certain steps in production are desirably adhered to maintain process efficiencies. For example, typically about 30 gallons of water is required for every bushel of grain used to produce alcohol.
  • conversion to alcohol is increased by using large amounts of water to encourage a rapid rolling boil. Accordingly, there is an ongoing need for techniques to increase efficiencies in alcohol production systems.
  • An aspect of the disclosure is directed to a production system that includes an electrolysis cell configured to electrochemically activate a received liquid, a slurry cooker configured to mix the electrochemically-activated liquid and feedstock granules to form a slurry, a fermentation vessel configured to receive the slurry in a hydrolyzed state and to produce a liquid mixture from the hydrolyzed slurry, where the liquid mixture includes water and alcohol, and a distillation assembly configured to separate at least a portion of the alcohol of the liquid mixture from the water of the liquid mixture.
  • Another aspect of the disclosure is directed to a process for producing an alcohol product.
  • the process includes heating an electrochemically-activated liquid and feedstock granules in a slurry cooker to form a slurry, where the electrochemically-activated liquid at least partially solvates the feedstock granules.
  • the process further includes hydrolyzing the slurry, fermenting the hydrolyzed slurry to form a liquid mixture that includes water and alcohol, and separating the alcohol of the liquid mixture from the water of the liquid mixture in a distillation assembly.
  • a further aspect of the disclosure is directed to a process for producing an alcohol product.
  • the process includes electrochemically activating a liquid mixture comprising water and alcohol, feeding the electrochemically-activated liquid mixture to a distillation assembly, and separating the alcohol of the electrochemically-activated liquid mixture from the water of the electrochemically-activated liquid mixture in the distillation assembly.
  • FIG. 1 is a schematic illustration of a production system for producing alcohol using an electrochemically-activated liquid.
  • FIG. 2 is a schematic illustration of an alternative production system for producing alcohol using an electrochemically-activated liquid, and further using an electrochemically-activated, alcohol/water mixture.
  • FIG. 3 is a schematic illustration of an electrolysis cell of the production system, where the electrolysis cell has a dual-chamber arrangement with an ion-exchange membrane.
  • FIG. 4 is a schematic illustration of an alternative electrolysis cell of the production system, where the alternative electrolysis cell includes a single-chamber arrangement without an ion-exchange membrane.
  • FIG. 5 is a flow diagram of a process for producing alcohol with an electrochemically-activated liquid.
  • FIG. 6 is a flow diagram of a process for producing alcohol with an electrochemically-activated liquid, and with an electrochemically-activated alcohol/water mixture.
  • An aspect of the present disclosure relates to systems and methods for producing alcohol, such as ethyl alcohol (CH 3 CH 2 OH), with the use of an electrochemically-activated liquid in the form of an alkaline liquid, an acidic liquid, or a blended combination of the alkaline and acidic species.
  • the electrochemically-activated liquid may be used for one or more stages of the alcohol production, and is particularly suitable for creating slurries with feedstock granules for hydrolysis reactions and fermentation.
  • the following discussion focuses on the use of water and electrochemically-activated water for producing alcohol, such as ethyl alcohol, with the understanding that a variety of different liquids may be used.
  • FIG. 1 is a schematic illustration of production system 10 , which illustrates an aspect of the present disclosure for producing alcohol (e.g., ethyl alcohol) using electrochemically-activated water.
  • production system 10 includes electrolysis cell 12 , feedstock mill 14 , slurry cooker 16 , fermentation tank 18 , solid/liquid (S/L) separator 20 , distillation assembly 22 , and collection tank 24 .
  • the illustration of production system 10 shown in FIG. 1 is simplified for ease of discussion, and production system 10 also desirably includes a variety of additional processing and regulatory components, such as fluid and gas pumps, filters, heat exchangers, valve assemblies, processing sensors (e.g., thermocouples), process-control mechanisms, and the like.
  • Electrolysis cell 12 is a fluid treatment cell that is adapted to apply an electric field across water (or other liquid) between at least one anode electrode and at least one cathode electrode.
  • Suitable cells for electrolysis cell 12 may have any suitable number of electrodes, and any suitable number of chambers for containing the water.
  • electrolysis cell 12 may include one or more ion exchange membranes between the anode and cathode, or can be configured without ion exchange membranes.
  • Electrolysis cell 12 may have a variety of different structures, such as, but not limited to those disclosed in Field et al., U.S. Patent Publication No. 2007/0186368, published Aug. 16, 2007.
  • production system 10 may include multiple electrolysis cells 12 that operate in series and/or parallel arrangements to electrochemically activate the water.
  • the water may be electrochemically activated from one or more external sources (e.g., one or more external electrolysis cells).
  • Water is supplied to electrolysis cell 12 through inlet line 26 , which correspondingly receives water from feed line 28 and recirculation line 30 .
  • Feed line 28 is a water line that provides fresh water from a supply source (not shown)
  • recirculation line 32 is a water line from distillation assembly 22 .
  • the water streams from feed line 28 and recirculation line 30 converge to supply water to inlet line 26 .
  • the water may flow through electrolytic cell 12 as separate streams.
  • inlet line 26 may separate into a pair of water lines, thereby separating the water into sub-streams prior to entering electrolytic cell 12 .
  • the water may be separated after entering electrolytic cell 12 .
  • the electric field applied across the water in electrolysis cell 12 electrochemically activates the water, which separates the water by collecting positive ions (i.e., cations, H + ) on one side of an electric circuit and collecting negative ions (i.e., anions, OH ⁇ ) on the opposing side.
  • the water having the cations is thereby rendered acidic and the water having the anions is correspondingly rendered alkaline.
  • the water may enter electrolysis cell 12 directly from inlet line 26 as a single stream.
  • the electrolysis process may also generate gas-phase bubbles, where the sizes of the gas-phase bubbles may vary depending on a variety of factors, such as the pressure through electrolysis cell 12 and the extent of the electrochemical activation. Accordingly, the gas-phase bubbles may have a variety of different sizes, including, but not limited to macrobubbles, microbubbles, nanobubbles, and mixtures thereof.
  • suitable average bubble diameters for the generated bubbles include diameters ranging from about 500 micrometers to about one millimeter.
  • examples of suitable average bubble diameters for the generated bubbles include diameters ranging from about one micrometer to less than about 500 micrometers.
  • examples of suitable average bubble diameters for the generated bubbles include diameters less than about one micrometer, with particularly suitable average bubble diameters including diameters less than about 500 nanometers, and with even more particularly suitable average bubble diameters including diameters less than about 100 nanometers.
  • the electrolysis process also restructures the water by breaking the water into smaller units that can penetrate cells much more efficiently than normal water. For example, most tap water and bottled water are made of large conglomerates of unstructured water molecules that are too large to move efficiently into cells.
  • the electrochemically-activated water is structured water that penetrates the cells at a much faster rate for better nutrient absorption and more efficient waste removal. Smaller water units also have a positive effect on the efficiency of metabolic processes.
  • outlet lines 32 and 34 the resulting streams of the electrochemically-activated water may exit electrolysis cell 12 through separate water lines (referred to as outlet lines 32 and 34 ).
  • Outlet line 32 interconnects electrolysis cell 12 and slurry cooker 16 , thereby directing the desired water product stream from electrolysis cell 12 to slurry cooker 16 .
  • Outlet line 34 is a purge line of the undesired water product stream, and may be discarded or recycled.
  • the water rendered acidic exits electrolysis cell 12 through outlet line 32 as the desired water product stream.
  • the resulting acidic water lacks electrons (i.e., oxidizing water) and has a high oxidation reduction potential.
  • the acidic water may function as an antibacterial agent, an antimicrobial agent, and/or an antifungal agent.
  • the water rendered alkaline exits electrolysis cell 12 through outlet line 34 as the undesired water product stream.
  • the water rendered alkaline exits electrolysis cell 12 through outlet line 32 as the desired water product stream.
  • the resulting alkaline water is abundant with electrons (i.e., reducing water), and has the capacity to neutralize free radicals at efficient rates.
  • the water rendered acidic exits electrolysis cell 12 through outlet line 34 as the undesired water product stream.
  • the water rendered acidic and the water rendered alkaline are recombined, and exit electrolysis cell 12 through outlet line 32 as the desired water product stream.
  • outlet line 34 may be omitted.
  • Feedstock mill 14 includes one or more mechanisms configured to grind received feedstock into fine powder granules for use in slurry cooker 16 .
  • Grain mill 14 may have a variety of different configurations for grinding the feedstock (e.g., a hammer mill).
  • Suitable feedstock for use in producing alcohol include materials containing sugars (e.g., sugar beets, sugar cane, sweet sorghum, and ripe fruits), starches (e.g., grains, potatoes, and Jerusalem artichokes), cellulose that may readily be convertible to fermentable sugars (e.g., stover, grasses, and wood), and combinations thereof.
  • feedstock mill 14 grinds the feedstock granules down to suitable particle sizes for suspending the feedstock granules in the electrochemically-activated water (within slurry cooker 16 ). After being ground, the resulting feedstock granules are relayed to slurry cooker 16 via transit line 36 .
  • Slurry cooker 16 includes one or more tanks in which the feedstock granules are mixed with the electrochemically-activated water and one or more enzymes (e.g., alpha-amylase enzymes) to prepare the feedstock granules for a hydrolysis reaction. Additional materials may also be added to the mixture (e.g., pH modifiers).
  • Suitable ratios of the feedstock granules to electrochemically-activated water may vary depending on a variety of factors, such as the type of feedstock used, the type of enzyme used, the cooking temperature, and the duration of cooking. Examples of suitable ratios of the feedstock granules to electrochemically-activated water range from about 2:1 to about 10:1, with particularly suitable ratios ranging from about 4:1 to about 8:1.
  • the resulting slurry is desirably heated for a suitable duration to attain a desired viscosity for subsequent processing.
  • Suitable elevated temperatures for the cooking process range from about 77° C. (about 170° F.) to about 93° C. (about 200° F.), with particularly suitable elevated temperatures ranging from about 82° C. (about 180° F.) to about 88° C. (about 190° F.).
  • Suitable durations for the cooking process range from about 15 minutes to about two hours, with particularly suitable durations ranging from about 30 minutes to about one hour.
  • the cations and/or the anions in the electrochemically-activated water assist in at least partially solvating the feedstock granules and enzymes in the liquid medium.
  • the cations and/or the anions of the water at least partially associate with various molecules of the feedstock granules and enzymes, thereby suspending the feedstock granules in the liquid medium.
  • the cations and/or anions may form ionic bonds with the hydroxyl (—OH) groups of the amylose and amylopectin components of starch chains. This is beneficial to prevent the feedstock granules from settling, which can otherwise reduce the uniformity of mixing with the enzymes. This may correspondingly reduce the percentage of conversion during the subsequent hydrolysis reaction.
  • Settling of the feedstock granules may also undesirably cause the feedstock granules to collect along the walls of slurry cooker 16 , which may reduce raw material efficiencies in production system 10 , and can potentially block passage of the resulting slurry from slurry cooker 16 after the cooking process is complete.
  • the slurry is also agitated during the cooking process to further assist in suspending the feedstock granules in the liquid medium, and to prevent the formation of hot spots in the slurry, which may otherwise scorch the feedstock granules.
  • slurry cooker 16 is configured to also function as a coolant heat exchanger to rapidly cool the slurry down.
  • the slurry may be transferred from slurry cooker 16 to a separate cooling unit (e.g., flash condensers, not shown). Additional electrochemically-activated water may also be added via outlet line 32 to assist in cooling the cooked slurry.
  • the slurry is reheated for a sufficient duration to allow the enzymes to break the starches down into smaller chains (e.g., dextrose and dextrin).
  • Suitable reheating temperatures for the hydrolysis reaction range from about 77° C. (about 170° F.) to about 93° C. (about 200° F.), with particularly suitable elevated temperatures ranging from about 82° C. (about 180° F.) to about 88° C. (about 190° F.).
  • Suitable durations for the hydrolysis reaction range from about 30 minutes to about four hours, with particularly suitable durations ranging from about one hour to about two hours.
  • Fermentation tank 18 includes one or more vessels configured to allow the hydrolyzed slurry to be further broken down into simple sugars with the use of one or more enzymes (e.g., glucoamylase). Yeast introduced into fermentation tank 18 then breaks down the simple sugars into ethyl alcohol and carbon dioxide, where the carbon dioxide may be purged from fermentation tank 18 through purge line 40 . Suitable durations for the fermentation process range from about 50 hours to about 75 hours. The resulting alcohol/water mixture, along with solids (e.g., grain and yeast residue), are then transferred to S/L separator 20 via transit line 42 .
  • enzymes e.g., glucoamylase
  • S/L separator 20 includes one or more separator units configured to separate the solids from the desired alcohol/water mixture. Suitable separator units for S/L separator 20 may incorporate a variety of separation techniques, and may include centrifuges, rotary screens, perforated tubing with augurs, and combinations thereof. The separated solids may exit S/L separator 20 via purge line 44 , and may be collected for further use (e.g., animal feed). The desired alcohol/water mixture is relayed to distillation assembly 22 through fluid line 46 .
  • Distillation assembly 22 includes one or more distillation columns (e.g., column 48 ), and one or more condensers and reboilers (e.g., condenser 50 and reboiler 52 ), and is configured to separate the water from the desired alcohol.
  • suitable distillation columns for column 48 include packed columns, perforated plate columns, bubble cap plate columns, and combinations thereof.
  • the alcohol/water mixture desirably enters column 52 at a mid-point location between the enriching and stripping sections. Because the water and the alcohol each have a fixed rate of vaporization, which varies with heat and is determined by the vapor pressure developed in a closed container to achieve equilibrium with the fluid, the alcohol can be separated from the water by controlling the heat applied to the mixture.
  • the vapor pressure of alcohol is higher than that of water, so the vapor pressure of the alcohol reaches an equilibrium with atmospheric pressure before the vapor pressure of water does.
  • the boiling point of the combination falls between the boiling points of the separate constituents (i.e., water boil at 100° C., and ethyl alcohol boils at 78.3° C.).
  • the ratio of the water to alcohol also determines the actual temperature of boiling for the mixture. Higher concentrations of alcohol lower the boiling point, and vice versa. As such, the temperature of the mixture will rise throughout the distillation run as the alcohol is drawn off.
  • the vapors given off by boiling a combination of the two will have a disproportionately large share of alcohol. For example, in a mixture that has 10% by volume ethyl alcohol and 90% by volume water, the vapors released will be about 80% by volume alcohol.
  • the vapors are condensed and revaporized using condenser 50 and reboiler 52 . Each redistillation increases the alcohol concentration of the batch until the liquid reaches the azeotropic limit.
  • the desired alcohol (e.g., ethyl alcohol) collected at the top of column 22 and condenser 50 may then be transferred to storage container 24 through fluid line 54 .
  • the desired alcohol may also pass through a molecular sieve to remove the water retained due to the azeotropic limit.
  • the separated water collected at the bottom of column 22 and reboiler 52 may then be purged via purge line 56 and/or recycled via recirculation line 30 .
  • the use of the electrochemically-activated water increases the suspension of the feedstock granules, thereby increasing the conversion rate of the hydrolyzed slurry into alcohol. This correspondingly reduces the amount of feedstock required to produce alcohol.
  • FIG. 2 is a schematic illustration of production system 110 , which is an alternative to production system 10 (shown in FIG. 1 ), and where reference labels for the respective components are increased by “100”.
  • production system 110 functions in the same manner as production system 10 to produce alcohol (e.g., ethyl alcohol) using electrochemically-activated water that is generated in electrolysis cell 112 .
  • production system 110 also includes electrolysis cell 158 disposed between S/L separator 120 and distillation assembly 122 .
  • Electrolysis cell 158 is a second fluid treatment cell that is adapted to apply an electric field across the alcohol/water mixture, between at least one anode electrode and at least one cathode electrode. Accordingly, electrolysis cell 158 may function in the same manner as electrolysis cell 12 (shown in FIG. 1 ), and suitable designs for electrolysis cell 158 include those discussed above for electrolysis cell 12 .
  • the alcohol/water mixture is supplied to electrolysis cell 158 through fluid line 146 .
  • the alcohol/water mixture may flow through electrolytic cell 158 as separate streams.
  • fluid line 146 may separate into a pair of fluid lines, thereby separating the alcohol/water mixture into sub-streams prior to entering electrolytic cell 158 .
  • the alcohol/water mixture may be separated after entering electrolytic cell 158 .
  • the electric field applied across the alcohol/water mixture in electrolysis cell 158 electrochemically activates the alcohol/water mixture, which separates the alcohol/water mixture by collecting cations on one side of an electric circuit and collecting anions on the opposing side.
  • the alcohol/water mixture may enter electrolysis cell 158 directly from inlet line 126 as a single stream.
  • the electrolysis process also desirably generates gas-phase bubbles, where the sizes of the gas-phase bubbles may vary depending on a variety of factors, such as the pressure through electrolysis cell 158 and the extent of the electrochemical activation. Accordingly, the gas-phase bubbles may have a variety of different sizes, including, but not limited to macrobubbles, microbubbles, nanobubbles, and mixtures thereof.
  • suitable average bubble diameters for the generated bubbles include diameters ranging from about 500 micrometers to about one millimeter.
  • examples of suitable average bubble diameters for the generated bubbles include diameters ranging from about one micrometer to less than about 500 micrometers.
  • examples of suitable average bubble diameters for the generated bubbles include diameters less than about one micrometer, with particularly suitable average bubble diameters including diameters less than about 500 nanometers, and with even more particularly suitable average bubble diameters including diameters less than about 100 nanometers.
  • the electrochemically-activated, alcohol/water mixture may then be recombined and directed to distillation assembly 122 via fluid line 160 .
  • the gas-phase bubbles desirably include high concentrations of the alcohol, thereby increasing the separation rate of the alcohol and the water in distillation assembly 122 . This increases the efficiency in operating distillation assembly 122 by reducing the duration and energy required to separate the alcohol from the water.
  • FIG. 3 is a schematic illustration of electrolysis cell 158 , which is also a suitable design for electrolysis cell 12 (shown in FIG. 1 ) and electrolysis cell 112 (shown in FIG. 2 ).
  • electrolysis cell 158 includes membrane 162 , which separates electrolysis cell 158 into anode chamber 164 and cathode chamber 166 .
  • electrolysis cell 158 is illustrated in FIG. 3 as having a single anode chamber and a single cathode chamber, electrolysis cell 158 may alternatively include a plurality of anode and cathode chambers separated by one or more membranes 162 .
  • Membrane 162 is an ion exchange membrane, such as a cation exchange membrane (i.e., a proton exchange membrane) or an anion exchange membrane.
  • Suitable cation exchange membranes for membrane 162 include partially and fully fluorinated ionomers, polyaromatic ionomers, and combinations thereof.
  • suitable commercially available ionomers for membrane 162 include sulfonated tetrafluorethylene copolymers available under the trademark “NAFION” from E.I.
  • Anode chamber 164 and cathode chamber 166 respectively include anode electrode 168 and cathode electrode 170 , where membrane 162 is disposed between anode electrode 168 and cathode electrode 170 .
  • Anode electrode 168 and cathode electrode 170 can be made from any suitable electrically-conductive material, such as titanium, and may be coated with one or more precious metals (e.g., platinum).
  • Anode electrode 168 and cathode electrode 170 may each also exhibit a variety of different geometric designs and constructions, such as flat plates, coaxial plates (e.g., for tubular electrolytic cells), rods, and combinations thereof; and may have solid constructions or can have one or more apertures (e.g., metallic meshes).
  • anode chamber 164 and cathode chamber 166 are each illustrated with a single anode electrode 168 and cathode electrode 170
  • anode chamber 164 may include a plurality of anode electrodes 168
  • cathode chamber 166 may include a plurality of cathode electrodes 170 .
  • Anode electrode 168 and cathode electrode 170 may be electrically connected to opposing terminals of a conventional power supply (not shown).
  • the power supply can provide electrolysis cell 158 with a constant direct-current (DC) output voltage, a pulsed or otherwise modulated DC output voltage, or a pulsed or otherwise modulated AC output voltage, to anode electrode 168 and cathode electrode 170 .
  • the power supply can have any suitable output voltage level, current level, duty cycle, or waveform. In one embodiment, the power supply applies the voltage supplied to anode electrode 168 and cathode electrode 170 at a relative steady state.
  • the power supply includes a DC/DC converter that uses a pulse-width modulation (PWM) control scheme to control voltage and current output.
  • PWM pulse-width modulation
  • anode electrode 168 and cathode electrode 170 may also be flipped during operation to remove any scales that potentially form on anode electrode 168 and cathode electrode 170 .
  • the alcohol/water mixture is supplied to electrolysis cell 158 from feed inlets 146 a and 146 b , which are the separated pathways of fluid line 146 .
  • the alcohol/water mixture flowing through feed inlet 146 a flows into anode chamber 164
  • the alcohol/water mixture flowing through feed inlet 146 b flows into cathode chamber 166 .
  • a voltage potential is applied to electrochemically activate the alcohol/water mixture flowing through anode chamber 164 and cathode chamber 166 .
  • membrane 162 is a cation exchange membrane
  • a suitable voltage e.g., a DC voltage
  • the actual potential required at any position within electrolytic cell 158 may be determined by the local composition of the alcohol/water mixture.
  • a greater potential difference i.e., over potential
  • Platinum-based electrodes typically require an addition of about one-half of a volt to the potential difference between the electrodes.
  • a further potential is desirable to drive the current through electrolytic cell 158 .
  • suitable applied voltage potentials for electrolysis cell 158 range from about 1 volt to about 40 volts, with particularly suitable voltages ranging from about 5 volts to about 25 volts, and with even more particularly suitable voltages ranging from about 10 volts to about 20 volts.
  • cations e.g., H +
  • anions e.g., OH ⁇
  • anions e.g., OH ⁇
  • membrane 162 prevents the transfer of the anions present in cathode chamber 166 . Therefore, the anions remain confined within cathode chamber 166 .
  • the anions in the alcohol/water mixture bind to the metal atoms (e.g., platinum atoms) at anode electrode 168
  • the cations in the alcohol/water mixture e.g., hydrogen
  • the metal atoms e.g., platinum atoms
  • These bound atoms diffuse around in two dimensions on the surfaces of the respective electrodes until they take part in further reactions.
  • Other atoms and polyatomic groups may also bind similarly to the surfaces of anode electrode 168 and cathode electrode 170 , and may also subsequently undergo reactions.
  • Molecules such as oxygen (O 2 ) and hydrogen (H 2 ) produced at the surfaces may enter small cavities in the liquid phase of the alcohol/water mixture (i.e., bubbles) as gases and/or may become solvated by the liquid phase of the alcohol/water mixture.
  • the gas-phase bubbles desirably include high concentrations of the alcohol, thereby increasing the separation rate of the alcohol and the water in distillation assembly 122 .
  • the gas contained in the nanobubbles are also believed to be stable for substantial durations in the liquid phase alcohol/water mixture, despite their small diameters. While not wishing to be bound by theory, it is believed that the surface tension of the alcohol/water mixture, at the gas/liquid interface, drops when curved surfaces of the gas bubbles approach molecular dimensions. This reduces the natural tendency of the nanobubbles to dissipate.
  • nanobubble gas/liquid interface is charged due to the voltage potential applied across membrane 162 .
  • the charge introduces an opposing force to the surface tension, which also slows or prevents the dissipation of the nanobubbles.
  • the presence of like charges at the interface reduces the apparent surface tension, with charge repulsion acting in the opposite direction to surface minimization due to surface tension. Any effect may be increased by the presence of additional charged materials that favor the gas/liquid interface.
  • catholyte nanobubbles are not likely to lose their charge on mixing with the anolyte sub-stream at the convergence point of fluid line 160 (shown in FIG. 2 ), and are otherwise stable for a duration that is greater than the residence time of the electrochemically-activated, alcohol/water mixture within fluid line 160 .
  • gas molecules may become charged within the nanobubbles (such as O 2 ⁇ ), due to the excess potential on the cathode, thereby increasing the overall charge of the nanobubbles.
  • the surface tension at the gas/liquid interface of charged nanobubbles can be reduced relative to uncharged nanobubbles, and their sizes stabilized. This can be qualitatively appreciated as surface tension causes surfaces to be minimized, whereas charged surfaces tend to expand to minimize repulsions between similar charges.
  • Raised temperature at the electrode surface due to the excess power loss over that required for the electrolysis, may also increase nanobubble formation by reducing local gas solubility.
  • the calculated charge density for zero excess internal pressure is 0.20, 0.14, 0.10, 0.06 and 0.04 e ⁇ /nanometer 2 bubble surface area, respectively.
  • Such charge densities are readily achievable with the use of electrolysis cell 24 .
  • the nanobubble radius increases as the total charge on the bubble increases to the power 2/3. Under these circumstances at equilibrium, the effective surface tension of the alcohol/water mixture at the nanobubble surface is zero, and the presence of charged gas in the bubble increases the size of the stable nanobubble. Further reduction in the bubble size would not be indicated as it would cause the reduction of the internal pressure to fall below atmospheric pressure.
  • the bubble is metastable if the overall energy change is negative which occurs when ⁇ E ST + ⁇ E q is negative, thereby providing:
  • the calculated charge density for bubble splitting 0.12, 0.08, 0.06, 0.04 and 0.03 e ⁇ /nanometer 2 bubble surface area respectively.
  • the bubble diameter is typically about three times larger for reducing the apparent surface tension to zero than for splitting the bubble in two.
  • the nanobubbles will generally not divide unless there is a further energy input.
  • the electrochemically-activated, alcohol/water mixture containing the gas-phase bubbles (e.g., macrobubbles, microbubbles, and nanobubbles), exits electrolysis cell 158 via feed outlets 160 a and 160 b , and the sub-streams re-converge at fluid line 160 prior to entering distillation assembly 148 .
  • the anolyte and catholyte fuels are blended prior to entering distillation assembly 148 , they are initially not in equilibrium and temporarily retain their electrochemically-activated states. Accordingly, the electrochemically-activated, alcohol/water mixture contains gas-phase bubbles dispersed/suspended in the liquid-phase alcohol/water mixture, which increases the separation efficiencies of the alcohol/water mixture within distillation assembly 122 .
  • FIG. 4 is a schematic illustration of electrolysis cell 172 , which is an example of an alternative electrolysis cell to cell 158 (shown in FIGS. 2 and 3 ) for electrochemically activating the alcohol/water mixture flowing through fluid line 146 , without the use of an ion exchange membrane.
  • Electrolysis cell 172 is also a suitable alternative design for electrolysis cell 12 (shown in FIG. 1 ) and electrolysis cell 112 (shown in FIG. 2 ) for electrochemically activating water for use in slurry cooker 16 (shown in FIG. 1 ) and slurry cooker 116 (shown in FIG. 2 ).
  • electrolysis cell 172 may engage directly with fluid lines 146 and 160 , and includes reaction chamber 174 , anode electrode 176 , and cathode electrode 178 .
  • Reaction chamber 174 can be defined by the walls of electrolysis cell 172 , by the walls of a container or conduit in which anode electrode 176 and cathode electrode 178 are placed, or by anode electrode 176 and cathode electrode 178 themselves. Suitable materials and constructions for anode electrode 176 and cathode electrode 178 include those discussed above for anode electrode 168 and cathode electrode 170 (shown in FIG. 3 ).
  • the alcohol/water mixture is introduced into reaction chamber 174 via feed line 146 , and a voltage potential is applied across anode electrode 176 and cathode electrode 178 .
  • This electrochemically activates the alcohol/water mixture where portions of the alcohol/water mixture near or in contact with anode electrode 176 and cathode electrode 178 generate gas-phase bubbles in the same manner as discussed above for electrolysis cell 158 .
  • the alcohol/water mixture flowing through electrolysis cell 172 contains gas-phase bubbles dispersed or otherwise suspended in the liquid-phase alcohol/water mixture.
  • the electrochemically-activated, alcohol/water mixture is blended during the entire electrolysis process, rather than being split upstream from, or within, the electrolysis cell, and then re-converged, or within, downstream from the electrolysis cell. Accordingly, the resulting electrochemically-activated, alcohol/water mixture contains gas-phase bubbles dispersed/suspended in the liquid-phase alcohol/water mixture, which increases the separation efficiencies of the alcohol/water mixture within distillation assembly 122 , as discussed above.
  • FIG. 5 is a flow diagram of process 180 for producing alcohol (e.g., ethyl alcohol) with an alcohol production system such as production system 10 (shown in FIG. 1 ).
  • Method 180 includes steps 182 - 194 , and initially involves milling a feedstock into fine powder granules for use in a slurry cooker (step 182 ).
  • One or more water streams are then supplied to an electrolysis cell, and, while the water streams flow through the electrolysis cell, a voltage potential is applied across anode and cathode electrodes and to the streams (step 184 ). As discussed above, this electrochemically activates the water.
  • the electrochemically-activated water is then combined with the milled feedstock to form a slurry, and the slurry is cooked in a slurry cooker (step 186 ).
  • the cations and/or the anions in the electrochemically-activated water assist in at least partially solvating the feedstock granules and enzymes in the liquid medium, thereby suspending the feedstock granules in the liquid medium. This is beneficial to prevent the feedstock granules from settling, which can otherwise reduce the uniformity of mixing with the enzymes, and reduce the percentage of conversion during a subsequent hydrolysis reaction.
  • the cooked slurry is hydrolyzed to break the feedstock materials (e.g., starch) into smaller chains (e.g., dextrose and dextrin) (step 188 ), and the hydrolyzed slurry is then fermented for a suitable duration to convert the hydrolyzed slurry into alcohol (e.g., ethyl alcohol) (step 190 ).
  • feedstock materials e.g., starch
  • chains e.g., dextrose and dextrin
  • the resulting alcohol/water mixture is desirably separated from the residual solids (step 192 ), and the alcohol/water mixture is distilled to at least partially separate the alcohol from the water (step 194 ).
  • electrochemically-activating the water increases the suspension of the feedstock granules, thereby increasing the rate of converting the hydrolyzed slurry into alcohol. This correspondingly reduces the amount of feedstock required to produce alcohol.
  • FIG. 6 is a flow diagram of process 196 for producing alcohol (e.g., ethyl alcohol) with an alcohol production system such as production system 110 (shown in FIG. 2 ).
  • Method 196 includes steps 198 - 212 , where steps 198 - 208 may be performed in the same manner as discussed above for steps 182 - 192 of process 180 (shown in FIG. 5 ).
  • process 196 further includes supplying one or more streams of the alcohol/water mixture to an electrolysis cell prior to feeding the mixture to the distillation assembly. While the alcohol/water mixture streams flow through the electrolysis cell, a voltage potential is applied across anode and cathode electrodes and to the streams (step 210 ).
  • the resulting electrochemically-activated, alcohol/water mixture is then distilled to at least partially separate the alcohol from the water (step 212 ).
  • the electrochemically-activated, alcohol/water mixture increases the separation efficiencies of the alcohol/water mixture within the distillation assembly, thereby increasing the operational efficiency of the distillation assembly.

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Water Treatment By Electricity Or Magnetism (AREA)
US12/140,864 2007-06-18 2008-06-17 System and process for producing alcohol Abandoned US20080308427A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/140,864 US20080308427A1 (en) 2007-06-18 2008-06-17 System and process for producing alcohol

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US94454707P 2007-06-18 2007-06-18
US12/140,864 US20080308427A1 (en) 2007-06-18 2008-06-17 System and process for producing alcohol

Publications (1)

Publication Number Publication Date
US20080308427A1 true US20080308427A1 (en) 2008-12-18

Family

ID=39708666

Family Applications (1)

Application Number Title Priority Date Filing Date
US12/140,864 Abandoned US20080308427A1 (en) 2007-06-18 2008-06-17 System and process for producing alcohol

Country Status (9)

Country Link
US (1) US20080308427A1 (es)
EP (1) EP2164973A1 (es)
JP (1) JP2010530244A (es)
KR (1) KR20100041773A (es)
CN (1) CN101743315A (es)
AU (1) AU2008266893A1 (es)
BR (1) BRPI0813674A2 (es)
MX (1) MX2009013743A (es)
WO (1) WO2008156736A1 (es)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120318659A1 (en) * 2011-06-20 2012-12-20 Piotr Medon Method and apparatus for dehydration of glycol
US20140332364A1 (en) * 2013-05-07 2014-11-13 Ja Energy, Inc. Modular distillation unit and ethanol separating apparatus

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20120010087A (ko) * 2008-04-25 2012-02-02 이-퓨얼 코포레이션 에탄올 생산을 위한 마이크로 정제 시스템
US20200017808A1 (en) * 2016-09-28 2020-01-16 Ebed Holdings Inc. Method and apparatus for producing an alcoholic beverage
US20230112608A1 (en) 2021-10-13 2023-04-13 Disruptive Oil And Gas Technologies Corp Nanobubble dispersions generated in electrochemically activated solutions

Citations (98)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3859195A (en) * 1972-09-20 1975-01-07 Du Pont Apparatus for electrochemical processing
US3897320A (en) * 1973-11-01 1975-07-29 Hooker Chemicals Plastics Corp Electrolytic manufacture of chlorates, using a plurality of electrolytic cells
US3933614A (en) * 1975-07-07 1976-01-20 Trienco, Inc. Pressure vessel for hydrogen generator
US4099489A (en) * 1975-10-06 1978-07-11 Bradley Curtis E Fuel regenerated non-polluting internal combustion engine
US4108052A (en) * 1975-12-04 1978-08-22 Cunningham Newton T Apparatus for producing alcohol from grains of starch materials
US4154578A (en) * 1977-08-01 1979-05-15 Bane William F Method and apparatus for cleaning a carpet on location
US4244079A (en) * 1979-02-09 1981-01-13 Bane William F Apparatus for cleaning a carpet on location
US4324635A (en) * 1980-08-25 1982-04-13 Sweeney Charles T Generation of chlorine-chlorine dioxide mixtures
US4374711A (en) * 1980-01-30 1983-02-22 Asahi Kasei Kogyo Kabushiki Kaisha Process for the electrolysis of an aqueous sodium chloride solution comprising, in combination, a diaphragm process and a cation exchange membrane process
US4502929A (en) * 1981-06-12 1985-03-05 Raychem Corporation Corrosion protection method
US4603167A (en) * 1985-02-19 1986-07-29 Xerox Corporation Bead polymerization process for toner resin compositions
US4663091A (en) * 1984-10-23 1987-05-05 Sam Sung Electronic Co., Ltd. Humidifier for removing bacilli from water
US4670113A (en) * 1984-10-30 1987-06-02 Lewis Arlin C Electrochemical activation of chemical reactions
US4676882A (en) * 1985-09-24 1987-06-30 Tatsuo Okazaki Electrolysis unit with membrane support means
US4687558A (en) * 1984-07-02 1987-08-18 Olin Corporation High current density cell
US4810344A (en) * 1987-03-11 1989-03-07 Omco Co., Ltd. Water electrolyzing apparatus
US4832230A (en) * 1987-12-15 1989-05-23 Janowitz C Michael Threaded cap containing additive for containers
US5186860A (en) * 1990-05-23 1993-02-16 Amp Incorporated Inert electrode comprising a conductive coating polymer blend formed of polyanisidine and polyacrylonitrile
US5292406A (en) * 1991-02-05 1994-03-08 Eka Nobel Ab Process for electrolytic production of alkali metal chlorate and auxiliary chemicals
US5316646A (en) * 1991-09-10 1994-05-31 Janix Kabushiki Kaisha Controlling apparatus for continuous electrolytic ion water producing apparatus
US5320718A (en) * 1990-08-07 1994-06-14 United Technologies Corporation Method for removing oxidizable organic compounds from an aqueous solution
US5378339A (en) * 1992-01-30 1995-01-03 Techno Excel Kabushiki Kaisha Water electrolyzer
US5536389A (en) * 1994-03-16 1996-07-16 Commissariat A L'energie Atomique Process and installation for the destruction of organic solutes, particularly complexing agents, present in an aqueous solution such as a radioactive effluent
US5590439A (en) * 1994-01-14 1997-01-07 Famulus Apparatus for cleaning by spreading cleaning liquid and by suction of the used liquid
US5632870A (en) * 1994-05-13 1997-05-27 Kucherov; Yan R. Energy generation apparatus
US5733434A (en) * 1995-05-31 1998-03-31 Pre-Tech Co., Ltd. Apparatus and method for cleaning semiconductor wafers
US5762779A (en) * 1994-03-25 1998-06-09 Nec Corporation Method for producing electrolyzed water
US5766438A (en) * 1990-12-26 1998-06-16 Unitika, Ltd. Electrolyzer and a method of operating the same
US5779891A (en) * 1990-04-23 1998-07-14 Andelman; Marc D. Non-fouling flow through capacitor system
US5858202A (en) * 1996-01-30 1999-01-12 Zenkoku-Mokko-Kikai-Kan, Inc. Method for producing electrolytic water and apparatus for producing the same
US5858201A (en) * 1994-07-29 1999-01-12 Toto, Ltd. Strong acid sterilizing liquid containing hypochlorous acid at a low concentration, method and apparatus for generating same, and apparatus for generating and dispensing same
US5928505A (en) * 1996-11-26 1999-07-27 Matsushita Electric Works, Ltd. Device for purifying and dispensing water
US5931859A (en) * 1998-09-30 1999-08-03 Burke; Robert E. Facial toning system
US6016973A (en) * 1997-07-17 2000-01-25 Carpet Co-Op Of America Association Cleaner/rinse dispensing device for carpet cleaning mechanism
US6032655A (en) * 1998-06-01 2000-03-07 Kavonius; Eino John Combustion enhancer
US6059941A (en) * 1996-09-26 2000-05-09 Solenzara International Limited Apparatus for generating a sterilizing solution
US6088211A (en) * 1997-11-10 2000-07-11 Ion Systems, Inc. Safety circuitry for ion generator
US6101671A (en) * 1996-06-07 2000-08-15 Royal Appliance Mfg. Co. Wet mop and vacuum assembly
US6110353A (en) * 1997-04-11 2000-08-29 H20 Technologies, Ltd. Housing and method that provide extended resident time for dissolving generated oxygen into water
US6200434B1 (en) * 1998-02-27 2001-03-13 Amano Corporation Apparatus for producing electrolytic water
US6231747B1 (en) * 1998-08-24 2001-05-15 T.R.P. Co., Ltd. Sterilizing wet wiper and apparatus for supplying sterilizing wet wipers
US20010002500A1 (en) * 1995-11-06 2001-06-07 Kasen Timothy E. Upright water extraction cleaning machine
US20020023847A1 (en) * 2000-06-23 2002-02-28 Shinichi Natsume Cleansing system and method using water electrolysis
US20020027070A1 (en) * 2000-09-06 2002-03-07 Tominaga Mfg. Co. Apparatus for producing electrolyzed water
US20020032141A1 (en) * 2000-09-08 2002-03-14 Gene Harkins System and method to clean and disinfect hard surfaces using electrolyzed acidic water produced from a solution of NaCl
US6375827B1 (en) * 1999-02-04 2002-04-23 Permelec Electrode Ltd. Electrochemical treating method and apparatus
US6379628B2 (en) * 1998-06-05 2002-04-30 Nederlands Instituut Voor Zuivelonderzoek Pulsed electric field treatment system
US6425958B1 (en) * 2000-11-13 2002-07-30 Tennant Company All surface cleaner
US20020112314A1 (en) * 2000-09-08 2002-08-22 Gene Harkins System and method to clean and disinfect carpets, fabrics,and hard surfaces using electrolyzed alkaline water produced from a solution of NaCl
US20030001439A1 (en) * 2001-07-02 2003-01-02 Schur Henry B. Magnetohydrodynamic EMF generator
US6502766B1 (en) * 2000-07-24 2003-01-07 The Procter & Gamble Company Liquid sprayers
US20030062068A1 (en) * 2001-07-10 2003-04-03 Ko Hyung-Ho Method of and system for cleaning a semiconductor wafer simultaneously using electrolytically ionized water and diluted hydrofluoric acid
US20030070919A1 (en) * 2001-10-12 2003-04-17 Gilmore F. William Electrocoagulation reaction chamber and method
US20030102270A1 (en) * 2001-11-02 2003-06-05 Meinolf Schoeberl Device for electrochemical treatment of a liquid and process-technical arrangement having such a device and process for operating such a process-technical
US6585827B2 (en) * 2001-07-30 2003-07-01 Tennant Company Apparatus and method of use for cleaning a hard floor surface utilizing an aerated cleaning liquid
US20030159233A1 (en) * 2002-02-28 2003-08-28 Samsung Gwangju Electronics Co., Ltd. Canister-type vacuum cleaner
US20030159230A1 (en) * 2002-02-28 2003-08-28 Jang-Keun Oh Upright-type vacuum cleaner
US20030159231A1 (en) * 2002-02-28 2003-08-28 Jang-Keun Oh Upright type vacuum cleaner
US20040012913A1 (en) * 2000-10-02 2004-01-22 Andelman Marc D. Fringe-field capacitor electrode for electrochemical device
US20040011665A1 (en) * 2001-06-21 2004-01-22 Tomohito Koizumi Electrolyzing electrode and production method therefor and electrolysis method using electrolyzing electrode and electrolysis solution producing device
US6689262B2 (en) * 2002-02-22 2004-02-10 Aqua Innovation, Inc. Microbubbles of oxygen
US20040037737A1 (en) * 2000-07-07 2004-02-26 Marais Jacobus T Method of and equipment for washing, disinfecting and/or sterilizing health care devices
US6703785B2 (en) * 2001-06-27 2004-03-09 Andes Electric Co., Ltd. Negative ion generator
US6719891B2 (en) * 2001-11-21 2004-04-13 Ecolab Inc. Point-of-use generation of chlorinated alkaline cleaning solutions by electrolysis
US20040069611A1 (en) * 2000-12-16 2004-04-15 Macgregor Scott John Decontaminated fluids and biocidal liquids
US6735812B2 (en) * 2002-02-22 2004-05-18 Tennant Company Dual mode carpet cleaning apparatus utilizing an extraction device and a soil transfer cleaning medium
US20040112763A1 (en) * 2001-07-13 2004-06-17 Itoh Jin-Ichi Method for surface treatment of processed copper workpiece
US20040166019A1 (en) * 2001-09-10 2004-08-26 Christoph Schultheiss Method and reactor for the non-thermal decomposition and pasteurization of organic process materials by electroporation
US6842940B2 (en) * 2003-02-12 2005-01-18 Minuteman International, Inc. Floor scrubber
US6855233B2 (en) * 2002-11-15 2005-02-15 Kinji Sawada Apparatus for production of strong alkali and acid electrolytic solution
US6878287B1 (en) * 2000-02-04 2005-04-12 Radical Waters Ip (Pty) Limited Dental equipment and method of operating such equipment
US20050121334A1 (en) * 2001-12-05 2005-06-09 Osao Sumita Method and apparatus for producting negative and positive oxidative reductive potential (orp) water
US20050126928A1 (en) * 2002-03-06 2005-06-16 Yen-Con Hung Method and apparatus for electrolyzing water
US20050136520A1 (en) * 2003-10-03 2005-06-23 Kinley Michael T. Biomass conversion to alcohol using ultrasonic energy
US20050139239A1 (en) * 2003-10-13 2005-06-30 Prae Gary L. Electrostatic hand cleanser apparatus and method of use
US20050139808A1 (en) * 2003-12-30 2005-06-30 Oculus Innovative Sciences, Inc. Oxidative reductive potential water solution and process for producing same
US6921743B2 (en) * 2001-04-02 2005-07-26 The Procter & Gamble Company Automatic dishwashing compositions containing a halogen dioxide salt and methods for use with electrochemical cells and/or electrolytic devices
US6926819B2 (en) * 2001-05-25 2005-08-09 Omega Co. Ltd. Method for generating sterilizing wash water and a portable apparatus thereof
US20060037869A1 (en) * 2004-08-19 2006-02-23 Miox Corporation Scented electrolysis product
US7008523B2 (en) * 2001-07-16 2006-03-07 Miox Corporation Electrolytic cell for surface and point of use disinfection
US7011739B2 (en) * 2001-03-22 2006-03-14 Gene Harkins Method for sanitizing shells of eggs using electrolyzed oxidizing water
US20060076248A1 (en) * 2004-10-08 2006-04-13 Electric Aquagenics Unlimited Apparatus and method for producing electrolyzed water
US7059013B2 (en) * 2002-09-06 2006-06-13 Tennant Company Fluid recovery device
US20060162735A1 (en) * 2004-12-15 2006-07-27 L'oreal Applicator for make-up remover
US20060169575A1 (en) * 2005-02-03 2006-08-03 Osao Sumita Manufacturing method of oxidative water to be employed for sterilization
US7160472B2 (en) * 2002-11-19 2007-01-09 Xogen Technologies Inc. Treatment of a waste stream through production and utilization of oxyhydrogen gas
US20070023273A1 (en) * 2005-06-16 2007-02-01 Permelec Electrode Ltd. Method of sterilization and electrolytic water ejecting apparatus
US20070037267A1 (en) * 2005-05-02 2007-02-15 Broin And Associates, Inc. Methods and systems for producing ethanol using raw starch and fractionation
US7226542B2 (en) * 2003-08-22 2007-06-05 Anvik Corporation Fluid treatment apparatus
US20070141434A1 (en) * 2000-06-26 2007-06-21 Joshi Ashok V Sanitizing Device and Associated Method Using Electrochemically Produced Sanitizing Agents
US7238272B2 (en) * 2004-02-27 2007-07-03 Yoichi Sano Production of electrolytic water
US20070170072A1 (en) * 2006-01-25 2007-07-26 Shyu Wen S Electrolytic facility having pulses for killing germs and for removing fouling
US20070186367A1 (en) * 2006-02-10 2007-08-16 Tennant Company Mobile surface cleaner having a sparging device
US20090008268A1 (en) * 2006-02-17 2009-01-08 Peter Salathe Process for Production of a Disinfectant Through the Electrochemical Activation (Eca) of Water, a Disinfectant Produced in this Way and the Use Thereof
US20090127128A1 (en) * 2007-11-15 2009-05-21 Permelec Electrode Ltd. Membrane-electrode assembly, electrolytic cell employing the same, electrolytic-water sprayer, and method of sterilization
US20090162505A1 (en) * 2007-12-21 2009-06-25 Sun-Maid Growers Of California Power spraying of agricultural products with wrinkled skins
US20090184186A1 (en) * 2006-06-13 2009-07-23 Hiroshi Suda Electrostatically atomizing device
US20100189805A1 (en) * 2007-04-13 2010-07-29 Aquqgroup Ag Electrochemically treated water, method and device for the production thereof, and the use thereof as a disinfection agent

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL62822A0 (en) * 1980-05-30 1981-07-31 Ppg Industries Inc Fermentation process
JPS60105495A (ja) * 1983-11-11 1985-06-10 Shinryo Air Conditioning Co Ltd 微生物の生反応促進方法
WO1986006098A1 (en) * 1985-04-09 1986-10-23 Voest-Alpine Aktiengesellschaft Process for the simultaneous production of alcohol and protein-rich fodder

Patent Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3859195A (en) * 1972-09-20 1975-01-07 Du Pont Apparatus for electrochemical processing
US3897320A (en) * 1973-11-01 1975-07-29 Hooker Chemicals Plastics Corp Electrolytic manufacture of chlorates, using a plurality of electrolytic cells
US3933614A (en) * 1975-07-07 1976-01-20 Trienco, Inc. Pressure vessel for hydrogen generator
US4099489A (en) * 1975-10-06 1978-07-11 Bradley Curtis E Fuel regenerated non-polluting internal combustion engine
US4108052A (en) * 1975-12-04 1978-08-22 Cunningham Newton T Apparatus for producing alcohol from grains of starch materials
US4154578A (en) * 1977-08-01 1979-05-15 Bane William F Method and apparatus for cleaning a carpet on location
US4244079A (en) * 1979-02-09 1981-01-13 Bane William F Apparatus for cleaning a carpet on location
US4374711A (en) * 1980-01-30 1983-02-22 Asahi Kasei Kogyo Kabushiki Kaisha Process for the electrolysis of an aqueous sodium chloride solution comprising, in combination, a diaphragm process and a cation exchange membrane process
US4324635A (en) * 1980-08-25 1982-04-13 Sweeney Charles T Generation of chlorine-chlorine dioxide mixtures
US4502929A (en) * 1981-06-12 1985-03-05 Raychem Corporation Corrosion protection method
US4687558A (en) * 1984-07-02 1987-08-18 Olin Corporation High current density cell
US4663091A (en) * 1984-10-23 1987-05-05 Sam Sung Electronic Co., Ltd. Humidifier for removing bacilli from water
US4670113A (en) * 1984-10-30 1987-06-02 Lewis Arlin C Electrochemical activation of chemical reactions
US4603167A (en) * 1985-02-19 1986-07-29 Xerox Corporation Bead polymerization process for toner resin compositions
US4676882A (en) * 1985-09-24 1987-06-30 Tatsuo Okazaki Electrolysis unit with membrane support means
US4810344A (en) * 1987-03-11 1989-03-07 Omco Co., Ltd. Water electrolyzing apparatus
US4832230A (en) * 1987-12-15 1989-05-23 Janowitz C Michael Threaded cap containing additive for containers
US5779891A (en) * 1990-04-23 1998-07-14 Andelman; Marc D. Non-fouling flow through capacitor system
US5186860A (en) * 1990-05-23 1993-02-16 Amp Incorporated Inert electrode comprising a conductive coating polymer blend formed of polyanisidine and polyacrylonitrile
US5320718A (en) * 1990-08-07 1994-06-14 United Technologies Corporation Method for removing oxidizable organic compounds from an aqueous solution
US5766438A (en) * 1990-12-26 1998-06-16 Unitika, Ltd. Electrolyzer and a method of operating the same
US5292406A (en) * 1991-02-05 1994-03-08 Eka Nobel Ab Process for electrolytic production of alkali metal chlorate and auxiliary chemicals
US5316646A (en) * 1991-09-10 1994-05-31 Janix Kabushiki Kaisha Controlling apparatus for continuous electrolytic ion water producing apparatus
US5378339A (en) * 1992-01-30 1995-01-03 Techno Excel Kabushiki Kaisha Water electrolyzer
US5590439A (en) * 1994-01-14 1997-01-07 Famulus Apparatus for cleaning by spreading cleaning liquid and by suction of the used liquid
US5536389A (en) * 1994-03-16 1996-07-16 Commissariat A L'energie Atomique Process and installation for the destruction of organic solutes, particularly complexing agents, present in an aqueous solution such as a radioactive effluent
US5762779A (en) * 1994-03-25 1998-06-09 Nec Corporation Method for producing electrolyzed water
US5632870A (en) * 1994-05-13 1997-05-27 Kucherov; Yan R. Energy generation apparatus
US5858201A (en) * 1994-07-29 1999-01-12 Toto, Ltd. Strong acid sterilizing liquid containing hypochlorous acid at a low concentration, method and apparatus for generating same, and apparatus for generating and dispensing same
US5733434A (en) * 1995-05-31 1998-03-31 Pre-Tech Co., Ltd. Apparatus and method for cleaning semiconductor wafers
US20010002500A1 (en) * 1995-11-06 2001-06-07 Kasen Timothy E. Upright water extraction cleaning machine
US5858202A (en) * 1996-01-30 1999-01-12 Zenkoku-Mokko-Kikai-Kan, Inc. Method for producing electrolytic water and apparatus for producing the same
US6101671A (en) * 1996-06-07 2000-08-15 Royal Appliance Mfg. Co. Wet mop and vacuum assembly
US6059941A (en) * 1996-09-26 2000-05-09 Solenzara International Limited Apparatus for generating a sterilizing solution
US5928505A (en) * 1996-11-26 1999-07-27 Matsushita Electric Works, Ltd. Device for purifying and dispensing water
US6110353A (en) * 1997-04-11 2000-08-29 H20 Technologies, Ltd. Housing and method that provide extended resident time for dissolving generated oxygen into water
US6016973A (en) * 1997-07-17 2000-01-25 Carpet Co-Op Of America Association Cleaner/rinse dispensing device for carpet cleaning mechanism
US6088211A (en) * 1997-11-10 2000-07-11 Ion Systems, Inc. Safety circuitry for ion generator
US6200434B1 (en) * 1998-02-27 2001-03-13 Amano Corporation Apparatus for producing electrolytic water
US6032655A (en) * 1998-06-01 2000-03-07 Kavonius; Eino John Combustion enhancer
US6379628B2 (en) * 1998-06-05 2002-04-30 Nederlands Instituut Voor Zuivelonderzoek Pulsed electric field treatment system
US6231747B1 (en) * 1998-08-24 2001-05-15 T.R.P. Co., Ltd. Sterilizing wet wiper and apparatus for supplying sterilizing wet wipers
US5931859A (en) * 1998-09-30 1999-08-03 Burke; Robert E. Facial toning system
US6375827B1 (en) * 1999-02-04 2002-04-23 Permelec Electrode Ltd. Electrochemical treating method and apparatus
US6878287B1 (en) * 2000-02-04 2005-04-12 Radical Waters Ip (Pty) Limited Dental equipment and method of operating such equipment
US20020023847A1 (en) * 2000-06-23 2002-02-28 Shinichi Natsume Cleansing system and method using water electrolysis
US20070141434A1 (en) * 2000-06-26 2007-06-21 Joshi Ashok V Sanitizing Device and Associated Method Using Electrochemically Produced Sanitizing Agents
US20040037737A1 (en) * 2000-07-07 2004-02-26 Marais Jacobus T Method of and equipment for washing, disinfecting and/or sterilizing health care devices
US6502766B1 (en) * 2000-07-24 2003-01-07 The Procter & Gamble Company Liquid sprayers
US20020027070A1 (en) * 2000-09-06 2002-03-07 Tominaga Mfg. Co. Apparatus for producing electrolyzed water
US20020032141A1 (en) * 2000-09-08 2002-03-14 Gene Harkins System and method to clean and disinfect hard surfaces using electrolyzed acidic water produced from a solution of NaCl
US20020112314A1 (en) * 2000-09-08 2002-08-22 Gene Harkins System and method to clean and disinfect carpets, fabrics,and hard surfaces using electrolyzed alkaline water produced from a solution of NaCl
US20040012913A1 (en) * 2000-10-02 2004-01-22 Andelman Marc D. Fringe-field capacitor electrode for electrochemical device
US6425958B1 (en) * 2000-11-13 2002-07-30 Tennant Company All surface cleaner
US20040069611A1 (en) * 2000-12-16 2004-04-15 Macgregor Scott John Decontaminated fluids and biocidal liquids
US7011739B2 (en) * 2001-03-22 2006-03-14 Gene Harkins Method for sanitizing shells of eggs using electrolyzed oxidizing water
US6921743B2 (en) * 2001-04-02 2005-07-26 The Procter & Gamble Company Automatic dishwashing compositions containing a halogen dioxide salt and methods for use with electrochemical cells and/or electrolytic devices
US6926819B2 (en) * 2001-05-25 2005-08-09 Omega Co. Ltd. Method for generating sterilizing wash water and a portable apparatus thereof
US7156962B2 (en) * 2001-06-21 2007-01-02 Sanyo Electric Co., Ltd. Electrolyzing electrode and production method therefor and electrolysis method using electrolyzing electrode and electrolysis solution producing device
US20040011665A1 (en) * 2001-06-21 2004-01-22 Tomohito Koizumi Electrolyzing electrode and production method therefor and electrolysis method using electrolyzing electrode and electrolysis solution producing device
US6703785B2 (en) * 2001-06-27 2004-03-09 Andes Electric Co., Ltd. Negative ion generator
US20030001439A1 (en) * 2001-07-02 2003-01-02 Schur Henry B. Magnetohydrodynamic EMF generator
US20030062068A1 (en) * 2001-07-10 2003-04-03 Ko Hyung-Ho Method of and system for cleaning a semiconductor wafer simultaneously using electrolytically ionized water and diluted hydrofluoric acid
US20040112763A1 (en) * 2001-07-13 2004-06-17 Itoh Jin-Ichi Method for surface treatment of processed copper workpiece
US7008523B2 (en) * 2001-07-16 2006-03-07 Miox Corporation Electrolytic cell for surface and point of use disinfection
US6585827B2 (en) * 2001-07-30 2003-07-01 Tennant Company Apparatus and method of use for cleaning a hard floor surface utilizing an aerated cleaning liquid
US20040166019A1 (en) * 2001-09-10 2004-08-26 Christoph Schultheiss Method and reactor for the non-thermal decomposition and pasteurization of organic process materials by electroporation
US20030070919A1 (en) * 2001-10-12 2003-04-17 Gilmore F. William Electrocoagulation reaction chamber and method
US20030102270A1 (en) * 2001-11-02 2003-06-05 Meinolf Schoeberl Device for electrochemical treatment of a liquid and process-technical arrangement having such a device and process for operating such a process-technical
US6719891B2 (en) * 2001-11-21 2004-04-13 Ecolab Inc. Point-of-use generation of chlorinated alkaline cleaning solutions by electrolysis
US20050121334A1 (en) * 2001-12-05 2005-06-09 Osao Sumita Method and apparatus for producting negative and positive oxidative reductive potential (orp) water
US6735812B2 (en) * 2002-02-22 2004-05-18 Tennant Company Dual mode carpet cleaning apparatus utilizing an extraction device and a soil transfer cleaning medium
US6689262B2 (en) * 2002-02-22 2004-02-10 Aqua Innovation, Inc. Microbubbles of oxygen
US20030159231A1 (en) * 2002-02-28 2003-08-28 Jang-Keun Oh Upright type vacuum cleaner
US20030159230A1 (en) * 2002-02-28 2003-08-28 Jang-Keun Oh Upright-type vacuum cleaner
US20030159233A1 (en) * 2002-02-28 2003-08-28 Samsung Gwangju Electronics Co., Ltd. Canister-type vacuum cleaner
US20050126928A1 (en) * 2002-03-06 2005-06-16 Yen-Con Hung Method and apparatus for electrolyzing water
US7059013B2 (en) * 2002-09-06 2006-06-13 Tennant Company Fluid recovery device
US6855233B2 (en) * 2002-11-15 2005-02-15 Kinji Sawada Apparatus for production of strong alkali and acid electrolytic solution
US7160472B2 (en) * 2002-11-19 2007-01-09 Xogen Technologies Inc. Treatment of a waste stream through production and utilization of oxyhydrogen gas
US6842940B2 (en) * 2003-02-12 2005-01-18 Minuteman International, Inc. Floor scrubber
US7226542B2 (en) * 2003-08-22 2007-06-05 Anvik Corporation Fluid treatment apparatus
US20050136520A1 (en) * 2003-10-03 2005-06-23 Kinley Michael T. Biomass conversion to alcohol using ultrasonic energy
US20050139239A1 (en) * 2003-10-13 2005-06-30 Prae Gary L. Electrostatic hand cleanser apparatus and method of use
US20050139808A1 (en) * 2003-12-30 2005-06-30 Oculus Innovative Sciences, Inc. Oxidative reductive potential water solution and process for producing same
US7238272B2 (en) * 2004-02-27 2007-07-03 Yoichi Sano Production of electrolytic water
US20060037869A1 (en) * 2004-08-19 2006-02-23 Miox Corporation Scented electrolysis product
US20060076248A1 (en) * 2004-10-08 2006-04-13 Electric Aquagenics Unlimited Apparatus and method for producing electrolyzed water
US20060162735A1 (en) * 2004-12-15 2006-07-27 L'oreal Applicator for make-up remover
US20060169575A1 (en) * 2005-02-03 2006-08-03 Osao Sumita Manufacturing method of oxidative water to be employed for sterilization
US20070037267A1 (en) * 2005-05-02 2007-02-15 Broin And Associates, Inc. Methods and systems for producing ethanol using raw starch and fractionation
US20070023273A1 (en) * 2005-06-16 2007-02-01 Permelec Electrode Ltd. Method of sterilization and electrolytic water ejecting apparatus
US20070170072A1 (en) * 2006-01-25 2007-07-26 Shyu Wen S Electrolytic facility having pulses for killing germs and for removing fouling
US20070186367A1 (en) * 2006-02-10 2007-08-16 Tennant Company Mobile surface cleaner having a sparging device
US20090008268A1 (en) * 2006-02-17 2009-01-08 Peter Salathe Process for Production of a Disinfectant Through the Electrochemical Activation (Eca) of Water, a Disinfectant Produced in this Way and the Use Thereof
US20090184186A1 (en) * 2006-06-13 2009-07-23 Hiroshi Suda Electrostatically atomizing device
US20100189805A1 (en) * 2007-04-13 2010-07-29 Aquqgroup Ag Electrochemically treated water, method and device for the production thereof, and the use thereof as a disinfection agent
US20090127128A1 (en) * 2007-11-15 2009-05-21 Permelec Electrode Ltd. Membrane-electrode assembly, electrolytic cell employing the same, electrolytic-water sprayer, and method of sterilization
US20090162505A1 (en) * 2007-12-21 2009-06-25 Sun-Maid Growers Of California Power spraying of agricultural products with wrinkled skins

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120318659A1 (en) * 2011-06-20 2012-12-20 Piotr Medon Method and apparatus for dehydration of glycol
US9044691B2 (en) * 2011-06-20 2015-06-02 Piotr Medon Method and apparatus for dehydration of glycol
US20140332364A1 (en) * 2013-05-07 2014-11-13 Ja Energy, Inc. Modular distillation unit and ethanol separating apparatus

Also Published As

Publication number Publication date
MX2009013743A (es) 2010-02-17
BRPI0813674A2 (pt) 2015-01-06
AU2008266893A1 (en) 2008-12-24
CN101743315A (zh) 2010-06-16
KR20100041773A (ko) 2010-04-22
JP2010530244A (ja) 2010-09-09
WO2008156736A1 (en) 2008-12-24
EP2164973A1 (en) 2010-03-24

Similar Documents

Publication Publication Date Title
Merino‐Garcia et al. Productivity and selectivity of gas‐phase CO2 electroreduction to methane at copper nanoparticle‐based electrodes
EP2890798B1 (en) Method for obtaining saccharified biomass with radiation and electrodialysis
US5980703A (en) Electrolytic cell for producing acidic water and alkaline water
US20080308427A1 (en) System and process for producing alcohol
US20110315561A1 (en) Treatment of solutions or wastewater
Gong et al. The possibility of the desalination of actual 1, 3-propanediol fermentation broth by electrodialysis
JP2016532441A (ja) 有機物から水素、メタン、揮発性脂肪酸、およびアルコールを製造する方法およびシステム
Krawczyk et al. Membrane performance during ultrafiltration of a high-viscosity solution containing hemicelluloses from wheat bran
Karekar et al. Continuous in-situ extraction of acetic acid produced by Acetobacterium woodii during fermentation of hydrogen and carbon dioxide using Amberlite FPA53 ion exchange resins
BR102013021902A2 (pt) Método de produção de etanol e biogás, e, instalação de etanol para a produção de etanol e biogás
CN111472016A (zh) 一种电解回收硫酸钠废液制备双氧水的方法
Liang et al. High-efficiency recovery, regeneration and recycling of 1-ethyl-3-methylimidazolium hydrogen sulfate for levulinic acid production from sugarcane bagasse with membrane-based techniques
Hernandez et al. Selective extraction of medium-chain carboxylic acids by electrodialysis and phase separation
JP2011115061A (ja) セルロースの分解方法
Liang et al. Controllable recovery and regeneration of bio-derived ionic liquid choline acetate for biomass processing via bipolar membrane electrodialysis-based methodology
CN108083366A (zh) 一种利用低品位热能氧化降解有机废水的方法
Hou-Rui Key drivers influencing the large scale production of xylitol
WO2013022334A1 (en) Process for the production of organic acids from an integration of solar or fuel cell with electrodialysis system
JP6225183B2 (ja) 糖類の発酵によるアルコール生産方法
Valentino et al. Capacitive Deionization for the Extraction and Recovery of Butyrate
KR102003918B1 (ko) 에너지 저소비형 당과 산의 분리방법
RU2438766C1 (ru) Способ получения биологически активной питьевой воды с пониженным содержанием дейтерия
Li et al. The paired electrochemical synthesis of gluconic acid and sorbitol
Keller Fenton’s chemistry in biorefineries
US10125344B2 (en) Apparatus and method for bioenergy production using regenerated acid solution

Legal Events

Date Code Title Description
AS Assignment

Owner name: TENNANT COMPANY, MINNESOTA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:FIELD, BRUCE F.;REEL/FRAME:021131/0973

Effective date: 20080616

AS Assignment

Owner name: JPMORGAN CHASE BANK, NATIONAL ASSOCIATION, AS COLL

Free format text: SECURITY AGREEMENT;ASSIGNOR:TENNANT COMPANY;REEL/FRAME:022408/0546

Effective date: 20090304

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

AS Assignment

Owner name: TENNANT COMPANY, MINNESOTA

Free format text: RELEASE BY SECURED PARTY;ASSIGNOR:JPMORGAN CHASE BANK, NATIONAL ASSOCIATION;REEL/FRAME:034837/0525

Effective date: 20141202