US20060272956A1 - Dual hydrogen production apparatus - Google Patents
Dual hydrogen production apparatus Download PDFInfo
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- US20060272956A1 US20060272956A1 US11/443,889 US44388906A US2006272956A1 US 20060272956 A1 US20060272956 A1 US 20060272956A1 US 44388906 A US44388906 A US 44388906A US 2006272956 A1 US2006272956 A1 US 2006272956A1
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M21/00—Bioreactors or fermenters specially adapted for specific uses
- C12M21/04—Bioreactors or fermenters specially adapted for specific uses for producing gas, e.g. biogas
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M41/00—Means for regulation, monitoring, measurement or control, e.g. flow regulation
- C12M41/26—Means for regulation, monitoring, measurement or control, e.g. flow regulation of pH
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M41/00—Means for regulation, monitoring, measurement or control, e.g. flow regulation
- C12M41/28—Means for regulation, monitoring, measurement or control, e.g. flow regulation of redox potential
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M45/00—Means for pre-treatment of biological substances
- C12M45/20—Heating; Cooling
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
- C12M47/18—Gas cleaning, e.g. scrubbers; Separation of different gases
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- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B1/00—Electrolytic production of inorganic compounds or non-metals
- C25B1/01—Products
- C25B1/02—Hydrogen or oxygen
- C25B1/04—Hydrogen or oxygen by electrolysis of water
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B9/00—Cells or assemblies of cells; Constructional parts of cells; Assemblies of constructional parts, e.g. electrode-diaphragm assemblies; Process-related cell features
- C25B9/70—Assemblies comprising two or more cells
- C25B9/73—Assemblies comprising two or more cells of the filter-press type
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/10—Process efficiency
- Y02P20/129—Energy recovery, e.g. by cogeneration, H2recovery or pressure recovery turbines
Definitions
- the present invention relates generally to a combination apparatus for concentrated production of hydrogen from hydrogen producing microorganism cultures. More particularly, the invention relates to a method that dually combines a primary hydrogen production apparatus with a secondary hydrogen production apparatus that is different than the primary hydrogen production apparatus.
- the primary hydrogen production apparatus uses heat or uses heat waste that is produced during typical usage of the secondary hydrogen production apparatus, thereby reducing energy costs of the primary hydrogen production apparatus and conserving energy.
- One possible method is to create hydrogen in a biological system by converting organic matter into hydrogen gas.
- the creation of a biogas that is substantially hydrogen can theoretically be achieved in a bioreactor, wherein hydrogen producing microorganisms and an organic feed material are held in an environment favorable to hydrogen production.
- Substantial and useful creation of hydrogen gas from microorganisms is problematic.
- the primary obstacle to sustained production of useful quantities of hydrogen by micro-organisms has been the eventual stoppage of hydrogen production generally coinciding with the appearance of methane. This occurs when methanogenic microorganisms invades the bioreactor environment converting hydrogen to methane. This process occurs naturally in anaerobic environments such as marshes, swamps, and pond sediments.
- continuous production of hydrogen from hydrogen producing micro-organisms has been unsuccessful in the past.
- Microbiologists have for many years known of organisms which generate hydrogen as a metabolic by-product. Two reviews of this body of knowledge are Kosaric and Lyng (1988) and Nandi and Sengupta (1998).
- the heterotrophic facultative anaerobes are of interest in this study, particularly those in the group known as the enteric microorganisms. Within this group are the mixed-acid fermenters, whose most well known member is Escherichia coli .
- one mole of glucose produces two moles of hydrogen gas.
- acetic and lactic acids also produced during the process are acetic and lactic acids, and minor amounts of succinic acid and ethanol.
- Other enteric microorganisms use a different enzyme pathway which causes additional CO 2 generation resulting in a 6:1 ratio of carbon dioxide to hydrogen production (Madigan et al., 1997).
- the hydrogen is typically converted into methane by methanogens.
- waste organic matter there are many sources of waste organic matter which could serve as a substrate for this microbial process.
- One such material would be organic-rich industrial wastewaters, particularly sugar-rich waters, such as fruit and vegetable processing wastes.
- Other sources include agricultural residues and other organic waste such as sewage and manures.
- Electrolysis is generally a chemical process in which chemically bonded elements are separated by passing an electrical current through them.
- An important application of electrolysis is in the separation of water into hydrogen and oxygen by the equation 2H 2 O ⁇ 2H 2 +O 2 .
- This reaction can occur on a highly simplified level, for example, by running two leads from a typical battery into water held in a cup. In this instance, as electricity is passed from one lead to another, preferably with the aid of a water soluble electrolyte, hydrogen and oxygen bubbles can be seen bubbling up from the water.
- electrolysis can create hydrogen on a larger scale in an electrolyzer. While an electrolyzer is functional at room temperature, doing so at an efficient level requires a high level of electrical energy. High temperature electrolyzers are more efficient than traditional room-temperature electrolyzers because some of the energy is supplied as heat, which is cheaper than electricity, and because the electrolysis reaction is more efficient at higher temperatures. Indeed, at 2500° C., electrical input is unnecessary because water breaks down to hydrogen and oxygen through thermolysis. As such temperatures are impractical, however; high temperature electrolyzers operate at about 100 to 1000° C. At higher temperature operating rates, lower levels of energy are required.
- Typical high temperature electrolyzers convey steam or super-heated water into an electrolytic cell having an anode and a cathode. This may occur in combination with hydrogen, for example, at about a 50-50 ratio of steam to hydrogen.
- the steam or water is split within the cell such that oxygen moves toward the anode and hydrogen moves toward the cathode.
- Remaining steam (if used), prior existing hydrogen and produced hydrogen exit the cell together, wherein hydrogen which can be separated from the steam by a condenser or other like apparatus. In either case, there is never a 100% efficient conversion of the water or steam to hydrogen, resulting in left over heated steam, water and/or oxygen.
- New apparatuses for hydrogen generation are therefore needed that produce substantial and useful levels of hydrogen in an inexpensive, environmentally sound apparatus that additionally dually combine differing hydrogen production apparatuses.
- An apparatus for dually producing hydrogen comprising: a secondary hydrogen production apparatus including an apparatus that breaks down chemical compounds, wherein hydrogen is produced from one or a series of reactions using heated liquids, vapors or gases, a primary hydrogen production apparatus operably combined with the secondary hydrogen production apparatus, the primary hydrogen production apparatus including a bioreactor adapted to produce hydrogen from microorganisms metabolizing an organic feed material, and a heat exchanger operably associated with the primary and secondary hydrogen production apparatuses such that heat from the secondary hydrogen production apparatus is transferred to the primary hydrogen production apparatus.
- FIG. 1 is a plan view of a primary hydrogen production apparatus proximate the secondary hydrogen production apparatus.
- FIG. 2 is a side view of one embodiment of the bioreactor.
- FIG. 3 is a plan view the bioreactor.
- FIG. 4 is a plan view of a secondary hydrogen production apparatus proximate the primary hydrogen production apparatus.
- FIG. 5 is a plan view of a high temperature secondary hydrogen production apparatus proximate the primary hydrogen production apparatus.
- microorganisms include bacteria and substantially microscopic cellular organisms.
- hydrophilicity As used herein, the term “hydrogen producing microorganisms” includes microorganisms that metabolize an organic substrate in one or a series of reactions that ultimately form hydrogen as one of the end products.
- methanogens refers to microorganisms that metabolize hydrogen in one or a series of reactions that produce methane as one of the end products.
- primary hydrogen production apparatus refers to a hydrogen producing process from hydrogen producing microorganisms in a bioreactor and related preparatory steps.
- secondary hydrogen production apparatus refers to a hydrogen producing process other than a bioreactor hydrogen producing process wherein heat waste resultant from the dual hydrogen producing process is used in the primary hydrogen production apparatus.
- heat waste refers to heat that is produced by dual hydrogen producing process that is otherwise not recycled into the dual hydrogen producing process such as excess heat or aqueous or gaseous compounds that have elevated temperatures, wherein some of the heat is diverted into another hydrogen producing process.
- FIG. 1 A dual hydrogen producing apparatus 100 in accordance with the present invention is shown in FIG. 1 , wherein primary hydrogen production apparatus 96 is shown in detail.
- primary hydrogen production apparatus 96 includes bioreactor 10 , heat exchanger 12 , optional equalization tank 14 and reservoir 16 .
- Apparatus 100 further includes secondary hydrogen production apparatus 50 , and passage 44 bridging primary hydrogen production apparatus 96 and secondary hydrogen production apparatus 50 .
- Apparatus 100 produces gas in bioreactor 10 , wherein the produced gas contains hydrogen and does not substantially include any methane.
- the hydrogen containing gas is produced by the metabolism of an organic feed material by hydrogen producing microorganisms.
- organic feed material is a sugar containing organic feed material.
- the organic feed material is industrial wastewater or effluent product that is produced during routine formation of fruit and/or vegetable juices, such as grape juice.
- wastewaters rich not only in sugars but also in protein and fats could be used, such as milk product wastes.
- the most complex potential source of energy for this process would be sewage-related wastes, such as municipal sewage sludge and animal manures.
- any feed containing organic material is usable in hydrogen production apparatus 100 .
- Hydrogen producing microorganisms can metabolize the sugars in the organic feed material under the reactions: Glucose ⁇ 2 Pyruvate (1) 2 Pyruvate+2 Coenzyme A ⁇ 2 Acetyl-CoA+2 HCOOH (2) 2 HCOOH ⁇ 2H 2 +2 CO 2 (3)
- one mole of glucose produces two moles of hydrogen gas and carbon dioxide.
- other organic feed materials include agricultural residues and other organic wastes such as sewage and manures. Typical hydrogen producing microorganisms are adept at metabolizing the high sugar organic waste into bacterial waste products.
- the wastewater may be further treated by aerating, diluting the solution with water or other dilutants, adding compounds that can control the pH of the solution or other treatment step.
- the solution may be supplemented with phosphorus (NaH 2 PO 4 ) or yeast extract.
- Organic feed material provides a plentiful feeding ground for hydrogen producing microorganisms and is naturally infested with these microorganisms. While hydrogen producing microorganisms typically occur naturally in an organic feed material, the organic feed material is preferably further inoculated with hydrogen producing microorganisms in an inoculation step. The inoculation may be an initial, one-time addition to bioreactor 10 at the beginning of the hydrogen production process. Further inoculations, however, may be added as desired. The added hydrogen producing microorganisms may include the same types of microorganisms that occur naturally in the organic feed material.
- the hydrogen producing microorganisms are preferably microorganisms that thrive in pH levels of about 3.5 to 6.0 and can survive in temperature of 60-100° F. or, more preferably, 60-75°.
- These hydrogen producing microorganisms include, but are not limited to, Clostridium sporogenes, Bacillus licheniformis and Kleibsiella oxytoca .
- Hydrogen producing microorganisms can be obtained from a microorganismal culture lab or like source. Other hydrogen producing microorganisms or microorganisms known in the art, however, can be used within the spirit of the invention.
- the inoculation step can occur in bioreactor 10 or elsewhere in the apparatus, for example, recirculation system 58 .
- Reservoir 16 is a container known in the art that can contain an organic feed material.
- the size, shape, and material of reservoir 16 can vary widely within the spirit of the invention.
- reservoir 16 is one or a multiplicity of storage tanks that are adaptable to receive, hold and store the organic feed material when not in use, wherein the one or a multiplicity of storage tanks may be mobile.
- reservoir 16 is a wastewater well that is adaptable to receive and contain wastewater and/or effluent from an industrial facility 50 .
- reservoir 16 is adaptable to receive and contain wastewater that is effluent from a juice manufacturing industrial facility 50 , such that the effluent held in the reservoir is a sugar rich juice sludge.
- Organic feed material contained in reservoir 16 can be removed through passage 22 with pump 28 .
- Pump 28 is in operable relation to reservoir 16 such that it aids removal movement of organic feed material 16 into passage 22 at a desired, adjustable flow rate, wherein pump 28 can be any pump known in the art suitable for pumping liquids.
- pump 28 is a submersible sump pump.
- Reservoir 16 may further include a low pH cutoff device 52 , such that exiting movement into passage 22 of the organic feed material is ceased if the pH of the organic feed material is outside of a desired range.
- the pH cutoff device 52 is a device known in the art operably related to reservoir 16 and pump 28 .
- the device ceases operation of pump 28 .
- the pH cut off in reservoir 16 is typically greater than the preferred pH of bioreactor 10 .
- the pH cutoff 52 is set between about 7 and 8 pH. In alternate embodiments, particularly when reservoir 16 is not adapted to receive effluent from an industrial facility 50 , the pH cutoff device is not used.
- Equalization tank is an optional intermediary container for holding organic feed material between reservoir 16 and heat exchanger 12 .
- Equalization tank 14 provides an intermediary container that can help control the flow rates of organic feed material into heat exchanger 12 by providing a slower flow rate into passage 20 than the flow rate of organic feed material into the equalization tank through passage 22 .
- the equalization tank can be formed of an), material suitable for holding and treating the organic feed material.
- equalization tank 14 is constructed of high density polyethylene materials. Other materials include, but are not limited to, metals or acrylics. Additionally, the size and shape of equalization tank 14 can vary widely within the spirit of the invention depending on throughput and output and location limitations.
- equalization tank 14 further includes a low level cut-off point device 56 .
- the low-level cut-off point device ceases operation of pump 26 if organic feed material contained in equalization tank 14 falls below a predetermined level. This prevents air from entering passage 20 .
- Organic feed material can be removed through passage 20 or through passage 24 .
- Passage 20 provides removal access from equalization tank 14 and entry access into heat exchanger 12 .
- Passage 24 provides removal access from equalization tank 14 of solution back to reservoir 16 .
- Passage 24 provides a removal system for excess organic feed material that exceeds the cut-off point of equalization tank 14 .
- Both passage 20 and passage 24 may further be operably related to pumps to facilitate movement of the organic feed material.
- equalization tank 14 is not used and organic feed material moves directly from reservoir 16 to heat exchanger 12 . In these embodiments, passages connecting reservoir 16 and heat exchanger 12 are arranged accordingly.
- the organic feed material is heated prior to conveyance into the bioreactor.
- the heating can occur anywhere upstream.
- the heating is achieved in one or a multiplicity of heat exchangers 12 , wherein the organic feed material is heated within the heat exchanger 12 by liquids or gasses of elevated temperatures from secondary hydrogen production apparatus 50 conveyed through passage 44 .
- Passage 44 may further be associated with a pump device to control flow rates.
- gases or liquids originally conveyed through passage 44 may be discarded through an effluent pipe (not pictured) or recycled back into the secondary hydrogen production apparatus.
- Organic feed solution can be additionally heated at additional or alternate locations in the hydrogen production apparatus.
- Passage 20 provides entry access to heat exchanger 12 , wherein heat exchanger 12 is any apparatus known in the art that can contain and heat contents held within it. Passage 20 is preferably operably related to pump 26 . Pump 26 aids the conveyance of solution from equalization tank 14 or reservoir 16 into heat exchanger 12 through passage 20 , wherein pump 26 is any pump known in the art suitable for this purpose. In preferred embodiments, pump 26 is an air driven pump for ideal safety reasons. However, motorized pumps are also found to be safe and are likewise usable.
- methanogens contained within the organic feed material are substantially killed or deactivated.
- the methanogens are substantially killed or deactivated prior to entry into the bioreactor.
- methanogens contained within the organic feed material are substantially killed or deactivated by being heated under elevated temperatures in heat exchanger 12 .
- Methanogens are substantially killed or deactivated by elevated temperatures. Methanogens are generally deactivated when heated to temperatures of about 60-75° C. for a period of at least 15 minutes. Additionally, methanogens are generally damaged or killed when heated to temperatures above about 90° C.
- Heat exchanger 12 enables heating of the organic feed material to temperature of about 60-100° C. in order to substantially deactivate or kill the methanogens while leaving any hydrogen producing microorganisms substantially functional. This effectively pasteurizes or sterilizes the contents of the organic feed material from active methanogens while leaving the hydrogen producing microorganisms intact, thus allowing the produced biogas to include hydrogen without subsequent conversion to methane.
- the size, shape and numbers of heat exchangers 12 can vary widely within the spirit of the invention depending on throughput and output required and location limitations.
- retention time in heat exchanger 12 is at least 20 minutes. Retention time marks the average time any particular part of organic feed material is retained in heat exchanger 12 .
- At least one temperature sensor 48 monitors a temperature indicative of the organic feed material temperature, preferably the temperature levels of equalization tank 14 and/or heat exchanger 12 .
- an electronic controller is provided having at least one microprocessor adapted to process signals from one or a plurality of devices providing organic feed material parameter information, wherein the electronic controller is operably related to the at least one actuatable terminal and is arranged to control the operation of and to controllably heat the heat exchanger 12 and/or any contents therein.
- the electronic controller is located or coupled to heat exchanger 12 or equalization tank 14 , or can alternatively be at a third or remote location. In alternate embodiments, the controller for controlling the temperature of heat exchanger 12 is not operably related to temperature sensor 48 .
- Passage 18 connects heat exchanger 12 with bioreactor 10 .
- Organic feed material is conveyed into the bioreactor through transport passage 18 at a desired flow rate.
- System 100 is a continuous flow system with organic feed material in constant motion between containers such as reservoir 16 , heat exchanger 12 , bioreactor 10 , equalization tank 14 if applicable, and so forth.
- Flow rates between the container can vary depending on retention time desired in any particular container. For example, in preferred embodiments, retention time in bioreactor 10 is between about 6 and 12 hours. To meet this retention time, the flow rate of passage 18 and effluent passage 36 are adjustable as known in the art so that organic feed material, on average, stays in bioreactor 10 for this period of time.
- passage 18 having a first and second end, wherein passage 18 provides entry access to the bioreactor at a first end of passage 18 and providing removal access to the heat exchanger 12 at a second end of passage 18 .
- Any type of passage known in the art can be used, such as a pipe or flexible tube.
- the transport passage may abut or extend within the bioreactor and/or the heat exchanger 12 .
- Passage 18 can generally provide access to bioreactor 10 at any location along the bioreactor. However, in preferred embodiments, passage 18 provides access at an upper portion of bioreactor 10 .
- Bioreactor 10 provides an anaerobic environment conducive for hydrogen producing microorganisms to grow, metabolize organic feed material, and produce hydrogen. While the bioreactor is beneficial to the growth of hydrogen producing microorganisms and the corresponding metabolism of organic feed material by the hydrogen producing microorganisms, it is preferably restrictive to the proliferation of unwanted microorganisms such as methanogens, wherein methanogens are microorganisms that metabolize carbon dioxide and hydrogen to produce methane and water. Methanogens are obviously unwanted as they metabolize hydrogen. If methanogens were to exist in substantial quantities in bioreactor 10 , hydrogen produced by the hydrogen producing bacteria will subsequently be converted to methane, reducing the percentage of hydrogen in the produced gas.
- methanogens were to exist in substantial quantities in bioreactor 10 , hydrogen produced by the hydrogen producing bacteria will subsequently be converted to methane, reducing the percentage of hydrogen in the produced gas.
- Bioreactor 10 can be any receptacle known in the art for holding an organic feed material.
- Bioreactor 10 is substantially airtight, providing an anaerobic environment.
- Bioreactor 10 itself may contain several openings. However, these openings are covered with substantially airtight coverings or connections, such as passage 18 , thereby keeping the environment in bioreactor 10 substantially anaerobic.
- the receptacle will be a limiting factor for material that can be produced. The larger the receptacle, the more hydrogen producing bacteria containing organic feed material, and, by extension, hydrogen, can be produced. Therefore, the size and shape of the bioreactor can vary widely within the sprit of the invention depending on throughput and output and location limitations.
- Bioreactor 80 can be formed of any material suitable for holding an organic feed material and that can further create an airtight, anaerobic environment.
- bioreactor 10 is constructed of high density polyethylene materials. Other materials, including but not limited to metals or plastics can similarly be used.
- a generally silo-shaped bioreactor 80 has about a 300 gallon capacity with a generally conical bottom 84 .
- Stand 82 is adapted to hold cone bottom 84 and thereby hold bioreactor 80 in an upright position.
- the bioreactor 80 preferably includes one or a multiplicity of openings that provide a passage for supplying or removing contents from within the bioreactor.
- bioreactor 80 preferably includes a central opening covered by lid 86 .
- the capacity of bioreactor 80 can be readily scaled upward or downward depending on needs or space limitations.
- the bioreactor preferably provides a system to remove excess solution, as shown in FIGS. 1 and 3 .
- the bioreactor includes effluent passage 36 having an open first and second end that provides a passage from inside bioreactor 10 to outside the bioreactor.
- the first end of effluent passage 36 may abut bioreactor 10 or extend into the interior of bioreactor 10 . If effluent passage 36 extends into the interior of passage 10 , the effluent passage preferably extends upwards to generally upper portion of bioreactor 10 .
- Effluent passage 36 preferably extends from bioreactor 10 into a suitable location for effluent, such as a sewer or effluent container, wherein the excess organic feed material will be deposited through the open second end.
- Bioreactor 10 preferably contains one or a multiplicity of substrates 90 for providing surface area for attachment and growth of bacterial biofilms. Sizes and shapes of the one or a multiplicity of substrates 90 can vary widely, including but not limited to flat surfaces, pipes, rods, beads, slats, tubes, slides, screens, honeycombs, spheres, object with latticework, or other objects with holes bored through the surface. Numerous substrates can be used, for example, hundreds, as needed. The more successful the biofilm growth on the substrates, the more fixed state hydrogen production will be achieved. The fixed nature of the hydrogen producing microorganisms provide the sustain production of hydrogen in the bioreactor.
- Substrates 90 preferably are substantially free of interior spaces that potentially fill with gas.
- the bioreactor comprises about 100-300 pieces of 1′′ plastic media to provide surface area for attachment of the bacterial biofilm.
- substrates 90 are FlexiringTM Random Packing (Koch-Glitsch.) Some substrates 90 may be retained below the liquid surface by a retaining device, for example, a perforated acrylic plate. In this embodiment, substrates 90 have buoyancy, and float on the organic feed material.
- the buoyant substrates stay at the same general horizontal level while the organic feed material circulates, whereby providing greater access to the organic feed material by hydrogen producing microorganism- and nonparaffinophilic microorganism-containing biofilm growing on the substrates.
- a recirculation system 58 is provided in operable relation to bioreactor 10 .
- Recirculation system 58 enables circulation of organic feed material contained within bioreactor 10 by removing orgYanic feed material at one location in bioreactor 10 and reintroduces the removed organic feed material at a separate location in bioreactor 10 , thereby creating a directional flow in the bioreactor.
- the directional flow aids the microorganisms within the organic feed material in finding food sources and substrates on which to grown biofilms.
- removing organic feed material from a lower region of bioreactor 10 and reintroducing it at an upper region of bioreactor 10 would create a downward flow in bioreactor 10 .
- Removing organic feed material from an upper region of bioreactor 10 and reintroducing it at a lower region would create an up-flow in bioreactor 10 .
- recirculation system 58 is arranged to produce an up-flow of any solution contained in bioreactor 10 .
- Passage 60 provides removal access at a higher point than passage 62 provides entry access.
- Pump 30 facilitates movement from bioreactor 10 into passage 60 , from passage 60 into passage 62 , and from passage 62 back into bioreactor 10 , creating up-flow movement in bioreactor 10 .
- Pump 30 can be any pump known in the art for pumping organic feed material.
- pump 30 is an air driven centrifugal pump. Other arrangements can be used, however, while maintaining the spirit of the invention.
- a pump could be operably related to a single passage that extends from one located of the bioreactor to another.
- Bioreactor 10 may optionally be operably related to one or a multiplicity of treatment apparatuses for treating organic feed material contained within bioreactor 10 for the purpose of making the organic feed material more conducive to proliferation of hydrogen producing microorganisms.
- the one or a multiplicity of treatment apparatuses perform operations that include, but are to limited to, aerating the organic feed material, diluting the organic feed material with water or other dilutant, controlling the pH of the organic feed material, and adding additional chemical compounds to the organic feed material.
- the apparatus coupled to the bioreactor can be any apparatuses known in the art for incorporating these treatments.
- a dilution apparatus is a tank having a passage providing controllable entry access of a dilutant, such as water, into bioreactor 10 .
- An aerating apparatus is an apparatus known in the art that provides a flow of gas into bioreactor 10 , wherein the gas is typically air.
- a pH control apparatus is an apparatus known in the art for controlling a pH of a solution.
- chemical compounds added by treatment apparatuses include anti-fungal agents, phosphorous supplements, yeast extract or hydrogen producing microorganism inoculation.
- the one or a multiplicity of treatment apparatuses may be operably related to other parts of the bioreactor system.
- the treatment apparatuses are operably related to equalization tank 14 or recirculation system 58 .
- multiple treatment apparatus of the same type may be located at various points in the bioreactor system to provide treatments at desired locations.
- pH controller 34 monitors the pH level of contents contained within bioreactor 10 .
- the pH of the organic feed material in bioreactor 10 is maintained at about 3.5 to 6.0 pH, most preferably at about 4.5 to 5.5 pH, as shown in Table 2.
- pH controller 34 controllably monitors the pH level of the organic feed material and adjustably controls the pH of the solution if the solution falls out of or is in danger of falling out of the desired range. As shown in FIG.
- pH controller 34 monitors the pH level of contents contained in passage 62 , such as organic feed material, with pH sensor 64 .
- pH controller 34 can be operably related to any additional or alternative location that potentially holds organic feed material, for example, passage 60 , passage 62 or bioreactor 10 as shown in FIG. 3 .
- the pH of the organic feed material falls out of a desired range, the pH is preferably adjusted back into the desired range. Precise control of a pH level is necessary to provide an environment that enables at least some hydrogen producing bacteria to function while similarly providing an environment unfavorable to methanogens. This enables the novel concept of allowing microorganism reactions to create hydrogen without subsequently being overrun by methanogens that convert the hydrogen to methane.
- Control of pH of the organic feed material in the bioreactor can be achieved by any means known in the art.
- a pH controller 34 monitors the pH and can add a pH control solution from container 54 in an automated manner if the pH of the bioreactor solution moves out of a desired range.
- the pH monitor controls the bioreactor solution's pH through automated addition of a sodium or potassium hydroxide solution.
- a sodium or potassium hydroxide solution is an Etatron DLX pH monitoring device.
- Preferred ranges of pH for the bioreactor solution is between about 3.5 and 6.0, with a more preferred range between about 4.0 and 5.5 pH.
- the hydrogen producing reactions of hydrogen producing bacteria metabolizing organic feed material in bioreactor 10 can further be monitored by oxidation-reduction potential (ORP) sensor 32 .
- ORP sensor 32 monitors redox potential of organic feed material contained within bioreactor 10 . Once ORP drops below about ⁇ 200 mV, gas production commences. Subsequently while operating in a continuous flow mode, the ORP was typically in the range of ⁇ 300 to ⁇ 450 mV.
- the wastewater is a grape juice solution prepared using Welch's Concord Grape JuiceTM diluted in tap water at approximately 32 mL of juice per Liter.
- the solution uses chlorine-free tap water or is aerated previously for 24 hours to substantially remove chlorine. Due to the acidity of the juice, the pH of the organic feed material is typically around 4.0.
- the constitutional make-up of the grape juice solution is shown in Table 1. TABLE 1 Composition of concord grape juice. Source: Welch's Company, personal comm., 2005.
- Bioreactor 10 further preferably includes an overflow cut-off switch 66 to turn off pump 26 if the solution exceeds or falls below a certain level in the bioreactor.
- Bioreactor 10 further includes an apparatus for capturing the hydrogen containing gas produced by the hydrogen producing bacteria. Capture and cleaning methods can vary widely within the spirit of the invention.
- gas is removed from bioreactor 10 through passage 38 , wherein passage 38 is any passage known in the art suitable for conveying a gaseous product.
- Pump 40 is operably related to passage 38 to aid the removal of gas from bioreactor 10 while maintaining a slight negative pressure in the bioreactor.
- pump 40 is an air driven pump.
- the gas is conveyed to gas scrubber 42 , where hydrogen is separated from carbon dioxide. Other apparatuses for separating hydrogen from carbon dioxide may likewise be used.
- the volume of collected gas can be measured by water displacement before and after scrubbing with concentrated NaOH.
- Samples of scrubbed and dried gas may be analyzed for hydrogen and methane by gas chromatography with a thermal conductivity detector (TCD) and/or with a flame ionization detector (FID). Both hydrogen and methane respond in the TCD, but the response to methane is improved in the FID (hydrogen is not detected by an FID, which uses hydrogen as a fuel for the flame).
- TCD thermal conductivity detector
- FID flame ionization detector
- Exhaust system 70 exhausts gas. Any exhaust system known in the art can be used. In a preferred embodiment, as shown in FIG. 1 , exhaust system includes exhaust passage 72 , backflow preventing device 74 , gas flow measurement and totalizer 76 , and air blower 46 .
- the organic feed material may be further inoculated in an initial inoculation step with one or a multiplicity of hydrogen producing bacteria, such as Clostridium sporogenes, Bacillus licheniformiis and Kleibsiella oxytoca , while contained in bioreactor 10 .
- hydrogen producing bacteria are obtained from a bacterial culture lab or like source.
- the hydrogen producing bacteria that occur naturally in the waste solution can be used without inoculating the solution.
- additional inoculations can occur in bioreactor 10 or other locations of the apparatus, for example, heat exchanger 12 , equalization tank 14 and reservoir 16 .
- the preferred hydrogen producing bacteria is Kleibsiella oxytoca , a facultative enteric bacterium capable of hydrogen generation.
- Kleibsiella oxytoca produces a substantially 1:1 ratio of hydrogen to carbon dioxide through organic feed material metabolization, not including impurities.
- the source of both the Kleibsiella ocytoca may be obtained from a source such yeast extract.
- the continuous input of seed organisms from the yeast extract in the waste solution results in a culture of Kleibsiella oxytoca in the bioreactor solution.
- the bioreactor may be directly inoculated with Kleibsiella oxyfoca .
- the inoculum for the bioreactor is a 48 h culture in nutrient broth added to diluted grape juice and the bioreactor was operated in batch mode until gas production commenced.
- the heating source preferably is heat exchanger 14 that uses heat or heat waste from dual hydrogen producing apparatus 16 to heat the organic feed material, wherein passage 44 is a bridge between the primary and secondary hydrogen production apparatus.
- Any heat exchanger known in the art designed for efficient heat transfer can be used in the apparatus including but not limited to parallel flow, counter flow, cross flow, shell and tube, plate, regenerative, adiabatic wheel, boiler and steam generator heat exchangers. Heat exchangers that heat a fluid separated from the heat source by a solid wall are preferred.
- the method preferably includes at least one temperature sensor for sensing a temperature indicative of the organic feed material temperature.
- an electronic controller is provided having at least one microprocessor adapted to process signals from one or a plurality of devices providing organic feed material parameter information, wherein the electronic controller is connected to the at least one actuatable terminal and is arranged to control the operation of and to controllably heat the heat exchanger 12 and/or any contents therein.
- the electronic controller operable related to heat exchanger 14 or heat exchanger 12 and may be located or coupled to those locations or be at a third or remote location.
- a heating source for system 100 preferably is heat exchanger 12 that uses heat or heat waste from industrial facility 50 to heat the organic feed material, wherein the heat exchanger is a heat exchanger known in the art.
- the heat exchanger can be a liquid phase-liquid phase or gas-phase/liquid phase as dictated by the phase of the heat waste.
- a typical heat exchanger for example, is a shell and tube heat exchanger which consists of a series of finned tubes, through which a first fluid runs. A second fluid runs over the finned tubes to be heated or cooled.
- Another type of heat exchanger is a plate heat exhanger, which directs flow through baffles so that fluids to be ehated and cooled are separated by plates with very large surface area.
- the secondary hydrogen production apparatus can include any hydrogen producing apparatus wherein that includes heat.
- the secondary hydrogen production apparatus is an apparatus that produces hydrogen with by separating H 2 O into hydrogen or water in one or a series of reactions.
- the secondary hydrogen production apparatus is an electrolyzer or a sulfur-iodine system.
- a steam based high temperature electrolyzer is combined with the primary hydrogen production apparatus 96 of the invention as shown in FIG. 4 .
- Electrolyzer 114 includes cell 102 having a cathode 104 and an anode 106 , wherein applied electrical current 112 is applied to the cell.
- the cell may further include a membrane 108 as needed.
- Steam and hydrogen stream 110 is conveyed into cell 102 , wherein the steam is heated at a temperature from about 100-1000° C.
- the amount of energy needed as a function of temperature is generally known in the art, as shown in Table 4.
- the thermal and electro forces will cause a portion of the water or steam to split, wherein oxygen will pass through ion conducting membrane 108 to the anode side and is removed on that side.
- the condenser can function as heat exchanger 12 or can be a separate condenser that functions in tandem with heat exchanger 12 . Either way, the heat exchanger 12 obtains heat from the steam that exits cell 102 and uses the heat to dually produce hydrogen in the primary hydrogen production apparatus by elevate the temperature of organic feed material to about 60 to 100° C.
- secondary hydrogen production apparatus is a high temperature electrolyzer that uses heated water, as in FIG. 5 .
- an electrical current is applied to cathode 116 and anode 118 under heated temperatures of about 100-1000° C., separating a portion of the heated water into oxygen and hydrogen.
- the oxygen migrates to the anode side across diaphragm 120 , while hydrogen migrates to the cathode side.
- Heat exchanger 12 can obtain heat from the heated water remaining the electrolyzer or by the released, heated oxygen.
- the secondary hydrogen production apparatus is a sulfur-iodide system.
- sulfuric acid is heated under high temperatures of about 750-1000° C. and low pressure under the reaction H 2 SO 4 ⁇ H 2 O+SO 2 +1/2O 2 .
- iodine can combine with the resultant sulfur dioxide and water under conditions known in the art under the reaction I 2 +SO 2 +2H 2 O ⁇ 2HI+H 2 SO 4 .
- the 2HI reacts with water and sulfur dioxide to under temperatures of about 350° C. to produce hydrogen and sulfur dioxide under the reaction 2HI ⁇ H 2 +I 2 .
- the net result of the process is the same as electrolysis: 2H 2 O ⁇ 2H 2 +O 2 .
- Heat exchanger 14 can use heat from any heat source from this process, for example, the heated H 2 SO 4 , heated H 2 O or oxygen. Regardless of where heat exchanger 44 acquires heat, the dual method enables two separate methods of hydrogen production, wherein the primary system uses heat energy from the secondary system in order to treat organic feed material for use in bioreactor 10 .
- the apparatus combines a bioreactor with a high temperature electrolyzer.
- the organic feed material is a grape juice waste product diluted in tap water at approximately 32 mL of juice per liter.
- the solution uses chlorine-free tap water or is aerated previously for 24 hours to substantially remove chlorine.
- the dilution and aeration occur in a treatment container.
- the organic feed material is then conveyed into the heat exchanger 12 through a passage.
- the organic feed material is heated in the heat exchanger 12 to about 65° C. for about 10 minutes to substantially deactivate methanogens.
- the organic feed material is heated with excess heat from the high temperature electrolyzer with a heat exchanger.
- the organic feed material is conveyed through a passage to the bioreactor wherein it is further inoculated with Kleibsiella oxytoca .
- the resultant biogases produced by the microorganisms metabolizing the organic feed material include hydrogen without any substantial methane.
- a multiplicity of reactors were initially operated at pH 4.0 and a flow rate of 2.5 mL min ⁇ 1 , resulting in a hydraulic retention time (HRT) of about 13 h (0.55 d). This is equivalent to a dilution rate of 1.8 d ⁇ 1 .
- the ORP ranged from ⁇ 300 to ⁇ 450 mV, total gas production averaged 1.6 L d ⁇ 1 and hydrogen production averaged 0.8 L d ⁇ 1 .
- the mean COD of the organic feed material during this period was 4,000 mg L ⁇ 1 and the mean effluent COD was 2,800 mg L ⁇ 1 , for a reduction of 30%.
- the molar H 2 production rate as a function of pH ranged from 0.32 to 2.05 moles of H 2 per mole of glucose consumed.
- the pathway appropriate to these organisms results in two moles of H 2 per mole of glucose, which was achieved at pH 5.0.
- the complete data set is provided in Tables 3a and 3b.
- hydrogen gas is generated using a microbial culture over a sustained period of time.
- the optimal pH for this culture consuming simple sugars from a simulated fruit juice bottling wastewater was found to be 5.0.
- a hydraulic residence time of about 0.5 days resulted in the generation of about 0.75 volumetric units of hydrogen gas per unit volume of reactor per day.
Abstract
The present invention provides an apparatus for the dual production of hydrogen, wherein organic feed material of a primary hydrogen production apparatus is heated with excess or diverted heat from a secondary hydrogen production apparatus, thereby substantially deactivating or killing methanogens within the organic feed material. Hydrogen producing microorganisms contained or added to the organic feed material metabolize the organic feed material in a bioreactor to produce hydrogen in a primary hydrogen production apparatus. As the methanogens are no longer substantially present to convert produced hydrogen to methane, a biogas that contains hydrogen without substantial methane can be produced.
Description
- This application claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application Ser. No. 60/685,851, filed May 31, 2005, entitled “COMBINATION BIOREACTOR AND ELECTROLYZER FOR PRODUCTION OF HYDROGEN”
- The present invention relates generally to a combination apparatus for concentrated production of hydrogen from hydrogen producing microorganism cultures. More particularly, the invention relates to a method that dually combines a primary hydrogen production apparatus with a secondary hydrogen production apparatus that is different than the primary hydrogen production apparatus. The primary hydrogen production apparatus uses heat or uses heat waste that is produced during typical usage of the secondary hydrogen production apparatus, thereby reducing energy costs of the primary hydrogen production apparatus and conserving energy.
- The production of hydrogen is an increasingly common and important procedure in the world today. Production of hydrogen in the U.S. alone currently amounts to about 3 billion cubic feet per year, with output likely to increase. Uses for the produced hydrogen are varied, ranging from uses in welding to production of hydrochloric acid. An increasingly important use of hydrogen relates to the production of alternative fuels for machinery such as motor vehicles. Successful use of hydrogen as an alternative fuel can provide substantial benefits to the world at large. This is important not only in that the hydrogen can be formed without dependence on the location of specific oils or other ground resources, but in that burning of hydrogen for fuel is atmospherically clean. Essentially, no carbon dioxide or greenhouse gasses are produced during the burning. Thus, production of hydrogen is an environmentally desirable goal.
- Creation of hydrogen from certain methods and apparatuses are generally known. For example, electrolysis, which generally involves the use of electricity to decompose water into hydrogen and oxygen, is a commonly used process. Significant energy, however, is required to produce the needed electricity to perform the process. Similarly, steam reforming is another expensive method requiring fossil fuels as an energy source. As could be readily understood, the environmental benefits of producing hydrogen are at least partially offset when using a process that uses pollution-causing fuels as an energy source for the production of hydrogen.
- New methods of hydrogen generation are therefore needed. One possible method is to create hydrogen in a biological system by converting organic matter into hydrogen gas. The creation of a biogas that is substantially hydrogen can theoretically be achieved in a bioreactor, wherein hydrogen producing microorganisms and an organic feed material are held in an environment favorable to hydrogen production. Substantial and useful creation of hydrogen gas from microorganisms, however, is problematic. The primary obstacle to sustained production of useful quantities of hydrogen by micro-organisms has been the eventual stoppage of hydrogen production generally coinciding with the appearance of methane. This occurs when methanogenic microorganisms invades the bioreactor environment converting hydrogen to methane. This process occurs naturally in anaerobic environments such as marshes, swamps, and pond sediments. As the appearance of methanogens in a biological system has previously been largely inevitable, continuous production of hydrogen from hydrogen producing micro-organisms has been unsuccessful in the past.
- Microbiologists have for many years known of organisms which generate hydrogen as a metabolic by-product. Two reviews of this body of knowledge are Kosaric and Lyng (1988) and Nandi and Sengupta (1998). Among the various organisms mentioned, the heterotrophic facultative anaerobes are of interest in this study, particularly those in the group known as the enteric microorganisms. Within this group are the mixed-acid fermenters, whose most well known member is Escherichia coli. While fermenting glucose, these micro-organisms split the glucose molecule forming two moles of pyruvate (Equation 1); an acetyl group is stripped from each pyruvate fragment leaving formic acid (Equation 2), which is then cleaved into equal amounts of carbon dioxide and hydrogen as shown in simplified form below Equation 3).
Glucose→2 Pyruvate (1)
2 Pyruvate+2 Coenzyme A→2 Acetyl-CoA+2 HCOOH (2)
2 HCOOH→2H2+2 CO2 (3) - Thus, during this process, one mole of glucose produces two moles of hydrogen gas. Also produced during the process are acetic and lactic acids, and minor amounts of succinic acid and ethanol. Other enteric microorganisms (the 2, 3 butanediol fermenters) use a different enzyme pathway which causes additional CO2 generation resulting in a 6:1 ratio of carbon dioxide to hydrogen production (Madigan et al., 1997). After this process, the hydrogen is typically converted into methane by methanogens.
- There are many sources of waste organic matter which could serve as a substrate for this microbial process. One such material would be organic-rich industrial wastewaters, particularly sugar-rich waters, such as fruit and vegetable processing wastes. Other sources include agricultural residues and other organic waste such as sewage and manures.
- Electrolysis is generally a chemical process in which chemically bonded elements are separated by passing an electrical current through them. An important application of electrolysis is in the separation of water into hydrogen and oxygen by the equation 2H2O→2H2+O2. This reaction can occur on a highly simplified level, for example, by running two leads from a typical battery into water held in a cup. In this instance, as electricity is passed from one lead to another, preferably with the aid of a water soluble electrolyte, hydrogen and oxygen bubbles can be seen bubbling up from the water.
- In more industrial applications, electrolysis can create hydrogen on a larger scale in an electrolyzer. While an electrolyzer is functional at room temperature, doing so at an efficient level requires a high level of electrical energy. High temperature electrolyzers are more efficient than traditional room-temperature electrolyzers because some of the energy is supplied as heat, which is cheaper than electricity, and because the electrolysis reaction is more efficient at higher temperatures. Indeed, at 2500° C., electrical input is unnecessary because water breaks down to hydrogen and oxygen through thermolysis. As such temperatures are impractical, however; high temperature electrolyzers operate at about 100 to 1000° C. At higher temperature operating rates, lower levels of energy are required.
- Typical high temperature electrolyzers convey steam or super-heated water into an electrolytic cell having an anode and a cathode. This may occur in combination with hydrogen, for example, at about a 50-50 ratio of steam to hydrogen. The steam or water is split within the cell such that oxygen moves toward the anode and hydrogen moves toward the cathode. Remaining steam (if used), prior existing hydrogen and produced hydrogen exit the cell together, wherein hydrogen which can be separated from the steam by a condenser or other like apparatus. In either case, there is never a 100% efficient conversion of the water or steam to hydrogen, resulting in left over heated steam, water and/or oxygen.
- In other industrial applications, hydrogen is produced through other reactions that occur at increased temperature levels. Usually in these instances, for economic production, high temperatures are required to ensure rapid throughput and high conversion efficiencies. (Transport and the Hydrogen Economy, UIC Nuclear Issues Briefing Paper # 73, October 2005) For example, in an sulfur-iodine system, sulfuric acid is heated under high temperature (800-1000° C.) and low pressure. The sulfuric acid breaks sown into water, oxygen and sulfur oxide, which combine with iodine to form 2HI and sulfuric acid. The 2HI reacts with water and sulfur dioxide to under temperatures of about 350° C. to produce hydrogen and sulfur dioxide. The net result of the equation is the same as electrolysis: 2H2O→2H2+O2. However, as not all compounds are converted, this process also results in heat or excess heat in the form of several solutions or gasses of elevated temperatures at elevated temperatures.
- New apparatuses for hydrogen generation are therefore needed that produce substantial and useful levels of hydrogen in an inexpensive, environmentally sound apparatus that additionally dually combine differing hydrogen production apparatuses.
- Therefore, it is an object of the present invention to create an apparatus of dual hydrogen production wherein hydrogen is produced in a primary system with hydrogen producing microorganisms by utilizing heat or heat waste from a secondary hydrogen production apparatus such as electrolysis to deactivate or kill methanogens that would otherwise metabolize the produced hydrogen.
- It is a further object of the invention to provide an apparatus for dually producing hydrogen An apparatus for dually producing hydrogen, comprising: a secondary hydrogen production apparatus including an apparatus that breaks down chemical compounds, wherein hydrogen is produced from one or a series of reactions using heated liquids, vapors or gases, a primary hydrogen production apparatus operably combined with the secondary hydrogen production apparatus, the primary hydrogen production apparatus including a bioreactor adapted to produce hydrogen from microorganisms metabolizing an organic feed material, and a heat exchanger operably associated with the primary and secondary hydrogen production apparatuses such that heat from the secondary hydrogen production apparatus is transferred to the primary hydrogen production apparatus.
- It is a further object of the invention to provide an apparatus wherein a bioreactor is readily combinable and proximate with secondary hydrogen production apparatus of varying types, the bioreactor utilizing heat or heat waste from the secondary hydrogen production apparatus with a heat exchanger bridge, wherein the hydrogen is not substantially converted to methane subsequent to production.
- It is a further object of the invention to heat the organic feed material prior to entry into the bioreactor, wherein heating is achieved in any one or a multiplicity of upstream containers or passages, such that heating the organic feed material at temperatures of about 60 to 100° C. kills or deactivates methanogens while leaving hydrogen producing microorganisms substantially intact.
- These and other objects of the present invention will become more readily apparent from the following detailed description and appended claims.
-
FIG. 1 is a plan view of a primary hydrogen production apparatus proximate the secondary hydrogen production apparatus. -
FIG. 2 is a side view of one embodiment of the bioreactor. -
FIG. 3 is a plan view the bioreactor. -
FIG. 4 is a plan view of a secondary hydrogen production apparatus proximate the primary hydrogen production apparatus. -
FIG. 5 is a plan view of a high temperature secondary hydrogen production apparatus proximate the primary hydrogen production apparatus. - As used herein, the term “microorganisms” include bacteria and substantially microscopic cellular organisms.
- As used herein, the term “hydrogen producing microorganisms” includes microorganisms that metabolize an organic substrate in one or a series of reactions that ultimately form hydrogen as one of the end products.
- As used herein, the term “methanogens” refers to microorganisms that metabolize hydrogen in one or a series of reactions that produce methane as one of the end products.
- As used herein, the term “primary hydrogen production apparatus” refers to a hydrogen producing process from hydrogen producing microorganisms in a bioreactor and related preparatory steps.
- As used herein, the term “secondary hydrogen production apparatus” refers to a hydrogen producing process other than a bioreactor hydrogen producing process wherein heat waste resultant from the dual hydrogen producing process is used in the primary hydrogen production apparatus.
- As used herein, the term “heat waste” refers to heat that is produced by dual hydrogen producing process that is otherwise not recycled into the dual hydrogen producing process such as excess heat or aqueous or gaseous compounds that have elevated temperatures, wherein some of the heat is diverted into another hydrogen producing process.
- A dual
hydrogen producing apparatus 100 in accordance with the present invention is shown inFIG. 1 , wherein primary hydrogen production apparatus 96 is shown in detail. As shown inFIG. 1 , primary hydrogen production apparatus 96 includesbioreactor 10,heat exchanger 12,optional equalization tank 14 andreservoir 16.Apparatus 100 further includes secondaryhydrogen production apparatus 50, andpassage 44 bridging primary hydrogen production apparatus 96 and secondaryhydrogen production apparatus 50.Apparatus 100 produces gas inbioreactor 10, wherein the produced gas contains hydrogen and does not substantially include any methane. The hydrogen containing gas is produced by the metabolism of an organic feed material by hydrogen producing microorganisms. - In preferred embodiments, organic feed material is a sugar containing organic feed material. In further preferred embodiments, the organic feed material is industrial wastewater or effluent product that is produced during routine formation of fruit and/or vegetable juices, such as grape juice. In additional embodiments, wastewaters rich not only in sugars but also in protein and fats could be used, such as milk product wastes. The most complex potential source of energy for this process would be sewage-related wastes, such as municipal sewage sludge and animal manures. However, any feed containing organic material is usable in
hydrogen production apparatus 100. Hydrogen producing microorganisms can metabolize the sugars in the organic feed material under the reactions:
Glucose→2 Pyruvate (1)
2 Pyruvate+2 Coenzyme A→2 Acetyl-CoA+2 HCOOH (2)
2 HCOOH→2H2+2 CO2 (3) - During this process, one mole of glucose produces two moles of hydrogen gas and carbon dioxide. In alternate embodiments, other organic feed materials include agricultural residues and other organic wastes such as sewage and manures. Typical hydrogen producing microorganisms are adept at metabolizing the high sugar organic waste into bacterial waste products. The wastewater may be further treated by aerating, diluting the solution with water or other dilutants, adding compounds that can control the pH of the solution or other treatment step. For example, the solution may be supplemented with phosphorus (NaH2PO4) or yeast extract.
- Organic feed material provides a plentiful feeding ground for hydrogen producing microorganisms and is naturally infested with these microorganisms. While hydrogen producing microorganisms typically occur naturally in an organic feed material, the organic feed material is preferably further inoculated with hydrogen producing microorganisms in an inoculation step. The inoculation may be an initial, one-time addition to
bioreactor 10 at the beginning of the hydrogen production process. Further inoculations, however, may be added as desired. The added hydrogen producing microorganisms may include the same types of microorganisms that occur naturally in the organic feed material. In preferred embodiments, the hydrogen producing microorganisms, whether occurring naturally or added in an inoculation step, are preferably microorganisms that thrive in pH levels of about 3.5 to 6.0 and can survive in temperature of 60-100° F. or, more preferably, 60-75°. These hydrogen producing microorganisms include, but are not limited to, Clostridium sporogenes, Bacillus licheniformis and Kleibsiella oxytoca. Hydrogen producing microorganisms can be obtained from a microorganismal culture lab or like source. Other hydrogen producing microorganisms or microorganisms known in the art, however, can be used within the spirit of the invention. The inoculation step can occur inbioreactor 10 or elsewhere in the apparatus, for example,recirculation system 58. -
Reservoir 16 is a container known in the art that can contain an organic feed material. The size, shape, and material ofreservoir 16 can vary widely within the spirit of the invention. In one embodiment,reservoir 16 is one or a multiplicity of storage tanks that are adaptable to receive, hold and store the organic feed material when not in use, wherein the one or a multiplicity of storage tanks may be mobile. In preferred embodiments,reservoir 16 is a wastewater well that is adaptable to receive and contain wastewater and/or effluent from anindustrial facility 50. In further preferred embodiments,reservoir 16 is adaptable to receive and contain wastewater that is effluent from a juice manufacturingindustrial facility 50, such that the effluent held in the reservoir is a sugar rich juice sludge. - Organic feed material contained in
reservoir 16 can be removed throughpassage 22 withpump 28.Pump 28 is in operable relation toreservoir 16 such that it aids removal movement oforganic feed material 16 intopassage 22 at a desired, adjustable flow rate, whereinpump 28 can be any pump known in the art suitable for pumping liquids. In a preferred embodiment, pump 28 is a submersible sump pump.Reservoir 16 may further include a lowpH cutoff device 52, such that exiting movement intopassage 22 of the organic feed material is ceased if the pH of the organic feed material is outside of a desired range. ThepH cutoff device 52 is a device known in the art operably related toreservoir 16 andpump 28. If the monitor detects a pH of a solution inreservoir 16 out of range, the device ceases operation ofpump 28. The pH cut off inreservoir 16 is typically greater than the preferred pH ofbioreactor 10. In preferred embodiments, thepH cutoff 52 is set between about 7 and 8 pH. In alternate embodiments, particularly whenreservoir 16 is not adapted to receive effluent from anindustrial facility 50, the pH cutoff device is not used. -
Passage 22 provides further entry access intoequalization tank 14 orheat exchanger 12. Equalization tank is an optional intermediary container for holding organic feed material betweenreservoir 16 andheat exchanger 12.Equalization tank 14 provides an intermediary container that can help control the flow rates of organic feed material intoheat exchanger 12 by providing a slower flow rate intopassage 20 than the flow rate of organic feed material into the equalization tank throughpassage 22. The equalization tank can be formed of an), material suitable for holding and treating the organic feed material. In the present invention,equalization tank 14 is constructed of high density polyethylene materials. Other materials include, but are not limited to, metals or acrylics. Additionally, the size and shape ofequalization tank 14 can vary widely within the spirit of the invention depending on throughput and output and location limitations. In preferred embodiments,equalization tank 14 further includes a low level cut-offpoint device 56. The low-level cut-off point device ceases operation ofpump 26 if organic feed material contained inequalization tank 14 falls below a predetermined level. This prevents air from enteringpassage 20. Organic feed material can be removed throughpassage 20 or throughpassage 24.Passage 20 provides removal access fromequalization tank 14 and entry access intoheat exchanger 12.Passage 24 provides removal access fromequalization tank 14 of solution back toreservoir 16.Passage 24 provides a removal system for excess organic feed material that exceeds the cut-off point ofequalization tank 14. Bothpassage 20 andpassage 24 may further be operably related to pumps to facilitate movement of the organic feed material. In alternate embodiments,equalization tank 14 is not used and organic feed material moves directly fromreservoir 16 toheat exchanger 12. In these embodiments,passages connecting reservoir 16 andheat exchanger 12 are arranged accordingly. - The organic feed material is heated prior to conveyance into the bioreactor. The heating can occur anywhere upstream. In one embodiment, the heating is achieved in one or a multiplicity of
heat exchangers 12, wherein the organic feed material is heated within theheat exchanger 12 by liquids or gasses of elevated temperatures from secondaryhydrogen production apparatus 50 conveyed throughpassage 44.Passage 44 may further be associated with a pump device to control flow rates. After exitingheat exchanger 12, gases or liquids originally conveyed throughpassage 44 may be discarded through an effluent pipe (not pictured) or recycled back into the secondary hydrogen production apparatus. Organic feed solution can be additionally heated at additional or alternate locations in the hydrogen production apparatus.Passage 20 provides entry access toheat exchanger 12, whereinheat exchanger 12 is any apparatus known in the art that can contain and heat contents held within it.Passage 20 is preferably operably related to pump 26.Pump 26 aids the conveyance of solution fromequalization tank 14 orreservoir 16 intoheat exchanger 12 throughpassage 20, whereinpump 26 is any pump known in the art suitable for this purpose. In preferred embodiments, pump 26 is an air driven pump for ideal safety reasons. However, motorized pumps are also found to be safe and are likewise usable. - To allow hydrogen producing microorganisms within the
bioreactor 10 to metabolize the organic feed material and produce hydrogen without subsequent conversion of the hydrogen to methane by methanogens, methanogens contained within the organic feed material are substantially killed or deactivated. In preferred embodiments, the methanogens are substantially killed or deactivated prior to entry into the bioreactor. In further preferred embodiments, methanogens contained within the organic feed material are substantially killed or deactivated by being heated under elevated temperatures inheat exchanger 12. Methanogens are substantially killed or deactivated by elevated temperatures. Methanogens are generally deactivated when heated to temperatures of about 60-75° C. for a period of at least 15 minutes. Additionally, methanogens are generally damaged or killed when heated to temperatures above about 90° C. for a period of at least 15 minutes.Heat exchanger 12 enables heating of the organic feed material to temperature of about 60-100° C. in order to substantially deactivate or kill the methanogens while leaving any hydrogen producing microorganisms substantially functional. This effectively pasteurizes or sterilizes the contents of the organic feed material from active methanogens while leaving the hydrogen producing microorganisms intact, thus allowing the produced biogas to include hydrogen without subsequent conversion to methane. The size, shape and numbers ofheat exchangers 12 can vary widely within the spirit of the invention depending on throughput and output required and location limitations. In preferred embodiments, retention time inheat exchanger 12 is at least 20 minutes. Retention time marks the average time any particular part of organic feed material is retained inheat exchanger 12. - At least one
temperature sensor 48 monitors a temperature indicative of the organic feed material temperature, preferably the temperature levels ofequalization tank 14 and/orheat exchanger 12. In preferred embodiments, an electronic controller is provided having at least one microprocessor adapted to process signals from one or a plurality of devices providing organic feed material parameter information, wherein the electronic controller is operably related to the at least one actuatable terminal and is arranged to control the operation of and to controllably heat theheat exchanger 12 and/or any contents therein. The electronic controller is located or coupled toheat exchanger 12 orequalization tank 14, or can alternatively be at a third or remote location. In alternate embodiments, the controller for controlling the temperature ofheat exchanger 12 is not operably related totemperature sensor 48. -
Passage 18 connectsheat exchanger 12 withbioreactor 10. Organic feed material is conveyed into the bioreactor throughtransport passage 18 at a desired flow rate.System 100 is a continuous flow system with organic feed material in constant motion between containers such asreservoir 16,heat exchanger 12,bioreactor 10,equalization tank 14 if applicable, and so forth. Flow rates between the container can vary depending on retention time desired in any particular container. For example, in preferred embodiments, retention time inbioreactor 10 is between about 6 and 12 hours. To meet this retention time, the flow rate ofpassage 18 andeffluent passage 36 are adjustable as known in the art so that organic feed material, on average, stays inbioreactor 10 for this period of time. - The organic feed material is conveyed through
passage 18 having a first and second end, whereinpassage 18 provides entry access to the bioreactor at a first end ofpassage 18 and providing removal access to theheat exchanger 12 at a second end ofpassage 18. Any type of passage known in the art can be used, such as a pipe or flexible tube. The transport passage may abut or extend within the bioreactor and/or theheat exchanger 12.Passage 18 can generally provide access tobioreactor 10 at any location along the bioreactor. However, in preferred embodiments,passage 18 provides access at an upper portion ofbioreactor 10. -
Bioreactor 10 provides an anaerobic environment conducive for hydrogen producing microorganisms to grow, metabolize organic feed material, and produce hydrogen. While the bioreactor is beneficial to the growth of hydrogen producing microorganisms and the corresponding metabolism of organic feed material by the hydrogen producing microorganisms, it is preferably restrictive to the proliferation of unwanted microorganisms such as methanogens, wherein methanogens are microorganisms that metabolize carbon dioxide and hydrogen to produce methane and water. Methanogens are obviously unwanted as they metabolize hydrogen. If methanogens were to exist in substantial quantities inbioreactor 10, hydrogen produced by the hydrogen producing bacteria will subsequently be converted to methane, reducing the percentage of hydrogen in the produced gas. -
Bioreactor 10 can be any receptacle known in the art for holding an organic feed material.Bioreactor 10 is substantially airtight, providing an anaerobic environment.Bioreactor 10 itself may contain several openings. However, these openings are covered with substantially airtight coverings or connections, such aspassage 18, thereby keeping the environment inbioreactor 10 substantially anaerobic. Generally, the receptacle will be a limiting factor for material that can be produced. The larger the receptacle, the more hydrogen producing bacteria containing organic feed material, and, by extension, hydrogen, can be produced. Therefore, the size and shape of the bioreactor can vary widely within the sprit of the invention depending on throughput and output and location limitations. - A preferred embodiment of a bioreactor is shown in
FIG. 2 .Bioreactor 80 can be formed of any material suitable for holding an organic feed material and that can further create an airtight, anaerobic environment. In the present invention,bioreactor 10 is constructed of high density polyethylene materials. Other materials, including but not limited to metals or plastics can similarly be used. A generally silo-shapedbioreactor 80 has about a 300 gallon capacity with a generally conical bottom 84.Stand 82 is adapted to hold cone bottom 84 and thereby holdbioreactor 80 in an upright position. Thebioreactor 80 preferably includes one or a multiplicity of openings that provide a passage for supplying or removing contents from within the bioreactor. The openings may further contain coverings known in the art that cover and uncover the openings as desired. For example,bioreactor 80 preferably includes a central opening covered bylid 86. In alternate embodiments of the invention, the capacity ofbioreactor 80 can be readily scaled upward or downward depending on needs or space limitations. - To maintain the solution volume level at a generally constant level, the bioreactor preferably provides a system to remove excess solution, as shown in
FIGS. 1 and 3 . In the present embodiment, the bioreactor includeseffluent passage 36 having an open first and second end that provides a passage frominside bioreactor 10 to outside the bioreactor. The first end ofeffluent passage 36 mayabut bioreactor 10 or extend into the interior ofbioreactor 10. Ifeffluent passage 36 extends into the interior ofpassage 10, the effluent passage preferably extends upwards to generally upper portion ofbioreactor 10. Whenbioreactor 10 is filled with organic feed material, the open first end of the effluent passage allows an excess organic feed material to be received byeffluent passage 36.Effluent passage 36 preferably extends frombioreactor 10 into a suitable location for effluent, such as a sewer or effluent container, wherein the excess organic feed material will be deposited through the open second end. -
Bioreactor 10 preferably contains one or a multiplicity ofsubstrates 90 for providing surface area for attachment and growth of bacterial biofilms. Sizes and shapes of the one or a multiplicity ofsubstrates 90 can vary widely, including but not limited to flat surfaces, pipes, rods, beads, slats, tubes, slides, screens, honeycombs, spheres, object with latticework, or other objects with holes bored through the surface. Numerous substrates can be used, for example, hundreds, as needed. The more successful the biofilm growth on the substrates, the more fixed state hydrogen production will be achieved. The fixed nature of the hydrogen producing microorganisms provide the sustain production of hydrogen in the bioreactor. -
Substrates 90 preferably are substantially free of interior spaces that potentially fill with gas. In the present embodiment, the bioreactor comprises about 100-300 pieces of 1″ plastic media to provide surface area for attachment of the bacterial biofilm. In one embodiment,substrates 90 are Flexiring™ Random Packing (Koch-Glitsch.) Somesubstrates 90 may be retained below the liquid surface by a retaining device, for example, a perforated acrylic plate. In this embodiment,substrates 90 have buoyancy, and float on the organic feed material. When a recirculation system is operably, the buoyant substrates stay at the same general horizontal level while the organic feed material circulates, whereby providing greater access to the organic feed material by hydrogen producing microorganism- and nonparaffinophilic microorganism-containing biofilm growing on the substrates. - In preferred embodiments, a
recirculation system 58 is provided in operable relation tobioreactor 10.Recirculation system 58 enables circulation of organic feed material contained withinbioreactor 10 by removing orgYanic feed material at one location inbioreactor 10 and reintroduces the removed organic feed material at a separate location inbioreactor 10, thereby creating a directional flow in the bioreactor. The directional flow aids the microorganisms within the organic feed material in finding food sources and substrates on which to grown biofilms. As could be readily understood, removing organic feed material from a lower region ofbioreactor 10 and reintroducing it at an upper region ofbioreactor 10 would create a downward flow inbioreactor 10. Removing organic feed material from an upper region ofbioreactor 10 and reintroducing it at a lower region would create an up-flow inbioreactor 10. - In preferred embodiments, as shown in
FIG. 1 ,recirculation system 58 is arranged to produce an up-flow of any solution contained inbioreactor 10.Passage 60 provides removal access at a higher point thanpassage 62 provides entry access.Pump 30 facilitates movement frombioreactor 10 intopassage 60, frompassage 60 intopassage 62, and frompassage 62 back intobioreactor 10, creating up-flow movement inbioreactor 10.Pump 30 can be any pump known in the art for pumping organic feed material. In preferred embodiments, pump 30 is an air driven centrifugal pump. Other arrangements can be used, however, while maintaining the spirit of the invention. For example, a pump could be operably related to a single passage that extends from one located of the bioreactor to another. -
Bioreactor 10 may optionally be operably related to one or a multiplicity of treatment apparatuses for treating organic feed material contained withinbioreactor 10 for the purpose of making the organic feed material more conducive to proliferation of hydrogen producing microorganisms. The one or a multiplicity of treatment apparatuses perform operations that include, but are to limited to, aerating the organic feed material, diluting the organic feed material with water or other dilutant, controlling the pH of the organic feed material, and adding additional chemical compounds to the organic feed material. The apparatus coupled to the bioreactor can be any apparatuses known in the art for incorporating these treatments. For example, in one embodiment, a dilution apparatus is a tank having a passage providing controllable entry access of a dilutant, such as water, intobioreactor 10. An aerating apparatus is an apparatus known in the art that provides a flow of gas intobioreactor 10, wherein the gas is typically air. A pH control apparatus is an apparatus known in the art for controlling a pH of a solution. Additionally chemical compounds added by treatment apparatuses include anti-fungal agents, phosphorous supplements, yeast extract or hydrogen producing microorganism inoculation. In other embodiments, the one or a multiplicity of treatment apparatuses may be operably related to other parts of the bioreactor system. For example, in one example, the treatment apparatuses are operably related toequalization tank 14 orrecirculation system 58. In still other embodiments, multiple treatment apparatus of the same type may be located at various points in the bioreactor system to provide treatments at desired locations. - Certain hydrogen producing bacteria proliferate in pH conditions that are not favorable to methanogens, for example, Kleibsiella oxytoca. Keeping organic feed material contained within
bioreactor 10 within this favorable pH range is conducive to hydrogen production. In preferred embodiments,pH controller 34 monitors the pH level of contents contained withinbioreactor 10. In preferred embodiments, the pH of the organic feed material inbioreactor 10 is maintained at about 3.5 to 6.0 pH, most preferably at about 4.5 to 5.5 pH, as shown in Table 2. In further preferred embodiments,pH controller 34 controllably monitors the pH level of the organic feed material and adjustably controls the pH of the solution if the solution falls out of or is in danger of falling out of the desired range. As shown inFIG. 1 ,pH controller 34 monitors the pH level of contents contained inpassage 62, such as organic feed material, with pH sensor 64. As could readily be understood,pH controller 34 can be operably related to any additional or alternative location that potentially holds organic feed material, for example,passage 60,passage 62 orbioreactor 10 as shown inFIG. 3 . - If the pH of the organic feed material falls out of a desired range, the pH is preferably adjusted back into the desired range. Precise control of a pH level is necessary to provide an environment that enables at least some hydrogen producing bacteria to function while similarly providing an environment unfavorable to methanogens. This enables the novel concept of allowing microorganism reactions to create hydrogen without subsequently being overrun by methanogens that convert the hydrogen to methane. Control of pH of the organic feed material in the bioreactor can be achieved by any means known in the art. In one embodiment, a
pH controller 34 monitors the pH and can add a pH control solution fromcontainer 54 in an automated manner if the pH of the bioreactor solution moves out of a desired range. In a preferred embodiment, the pH monitor controls the bioreactor solution's pH through automated addition of a sodium or potassium hydroxide solution. One such apparatus for achieving this is an Etatron DLX pH monitoring device. Preferred ranges of pH for the bioreactor solution is between about 3.5 and 6.0, with a more preferred range between about 4.0 and 5.5 pH. - The hydrogen producing reactions of hydrogen producing bacteria metabolizing organic feed material in
bioreactor 10 can further be monitored by oxidation-reduction potential (ORP)sensor 32.ORP sensor 32 monitors redox potential of organic feed material contained withinbioreactor 10. Once ORP drops below about −200 mV, gas production commences. Subsequently while operating in a continuous flow mode, the ORP was typically in the range of −300 to −450 mV. - In one embodiment, the wastewater is a grape juice solution prepared using Welch's Concord Grape Juice™ diluted in tap water at approximately 32 mL of juice per Liter. The solution uses chlorine-free tap water or is aerated previously for 24 hours to substantially remove chlorine. Due to the acidity of the juice, the pH of the organic feed material is typically around 4.0. The constitutional make-up of the grape juice solution is shown in Table 1.
TABLE 1 Composition of concord grape juice. Source: Welch's Company, personal comm., 2005. Concentration (unit indicated) Constituent Mean Range Carbohydrates1 15-18% glucose 6.2% 5-8% fructose 5.5% 5-8% sucrose 1.8% 0.2-2.3% maltose 1.9% 0-2.2% sorbitol 0.1% 0-0.2% Organic Acids1 0.5-1.7% Tartaric acid 0.84% 0.4-1.35% Malic acid 0.86% 0.17-1.54% Citric acid 0.044% 0.03-0.12% Minerals1 Calcium 17-34 mg/L Iron 0.4-0.8 mg/L Magnesium 6.3-11.2 mg/L Phosphorous 21-28 mg/L Potassium 175-260 mg/L Sodium 1-5 mg/L Copper 0.10-0.15 mg/L Manganese 0.04-0.12 mg/L Vitamins1 Vitamin C 4 mg/L Thiamine 0.06 mg/L Riboflavin 0.04 mg/L Niacin 0.2 mg/ L Vitamin A 80 I.U. pH 3.0-3.5 Total solids 18.5%
1additional trace constituents in these categories may be present.
-
Bioreactor 10 further preferably includes an overflow cut-off switch 66 to turn offpump 26 if the solution exceeds or falls below a certain level in the bioreactor. -
Bioreactor 10 further includes an apparatus for capturing the hydrogen containing gas produced by the hydrogen producing bacteria. Capture and cleaning methods can vary widely within the spirit of the invention. In the present embodiment, as shown inFIG. 1 , gas is removed frombioreactor 10 throughpassage 38, whereinpassage 38 is any passage known in the art suitable for conveying a gaseous product.Pump 40 is operably related topassage 38 to aid the removal of gas frombioreactor 10 while maintaining a slight negative pressure in the bioreactor. In preferred embodiments, pump 40 is an air driven pump. The gas is conveyed togas scrubber 42, where hydrogen is separated from carbon dioxide. Other apparatuses for separating hydrogen from carbon dioxide may likewise be used. The volume of collected gas can be measured by water displacement before and after scrubbing with concentrated NaOH. Samples of scrubbed and dried gas may be analyzed for hydrogen and methane by gas chromatography with a thermal conductivity detector (TCD) and/or with a flame ionization detector (FID). Both hydrogen and methane respond in the TCD, but the response to methane is improved in the FID (hydrogen is not detected by an FID, which uses hydrogen as a fuel for the flame). - Exhaust system 70 exhausts gas. Any exhaust system known in the art can be used. In a preferred embodiment, as shown in
FIG. 1 , exhaust system includesexhaust passage 72,backflow preventing device 74, gas flow measurement andtotalizer 76, andair blower 46. - The organic feed material may be further inoculated in an initial inoculation step with one or a multiplicity of hydrogen producing bacteria, such as Clostridium sporogenes, Bacillus licheniformiis and Kleibsiella oxytoca, while contained in
bioreactor 10. These hydrogen producing bacteria are obtained from a bacterial culture lab or like source. Alternatively, the hydrogen producing bacteria that occur naturally in the waste solution can be used without inoculating the solution. In further alternative embodiments, additional inoculations can occur inbioreactor 10 or other locations of the apparatus, for example,heat exchanger 12,equalization tank 14 andreservoir 16. - In the present embodiment, the preferred hydrogen producing bacteria is Kleibsiella oxytoca, a facultative enteric bacterium capable of hydrogen generation. Kleibsiella oxytoca produces a substantially 1:1 ratio of hydrogen to carbon dioxide through organic feed material metabolization, not including impurities. The source of both the Kleibsiella ocytoca may be obtained from a source such yeast extract. In one embodiment, the continuous input of seed organisms from the yeast extract in the waste solution results in a culture of Kleibsiella oxytoca in the bioreactor solution. Alternatively, the bioreactor may be directly inoculated with Kleibsiella oxyfoca. In one embodiment, the inoculum for the bioreactor is a 48 h culture in nutrient broth added to diluted grape juice and the bioreactor was operated in batch mode until gas production commenced.
- The heating source preferably is
heat exchanger 14 that uses heat or heat waste from dualhydrogen producing apparatus 16 to heat the organic feed material, whereinpassage 44 is a bridge between the primary and secondary hydrogen production apparatus. Any heat exchanger known in the art designed for efficient heat transfer can be used in the apparatus including but not limited to parallel flow, counter flow, cross flow, shell and tube, plate, regenerative, adiabatic wheel, boiler and steam generator heat exchangers. Heat exchangers that heat a fluid separated from the heat source by a solid wall are preferred. - The method preferably includes at least one temperature sensor for sensing a temperature indicative of the organic feed material temperature. In preferred embodiments, an electronic controller is provided having at least one microprocessor adapted to process signals from one or a plurality of devices providing organic feed material parameter information, wherein the electronic controller is connected to the at least one actuatable terminal and is arranged to control the operation of and to controllably heat the
heat exchanger 12 and/or any contents therein. The electronic controller operable related toheat exchanger 14 orheat exchanger 12 and may be located or coupled to those locations or be at a third or remote location. - A heating source for
system 100 preferably isheat exchanger 12 that uses heat or heat waste fromindustrial facility 50 to heat the organic feed material, wherein the heat exchanger is a heat exchanger known in the art. The heat exchanger can be a liquid phase-liquid phase or gas-phase/liquid phase as dictated by the phase of the heat waste. A typical heat exchanger, for example, is a shell and tube heat exchanger which consists of a series of finned tubes, through which a first fluid runs. A second fluid runs over the finned tubes to be heated or cooled. Another type of heat exchanger is a plate heat exhanger, which directs flow through baffles so that fluids to be ehated and cooled are separated by plates with very large surface area. - Heat is captured from secondary
hydrogen production apparatus 50 and is used to partially or fully heat the organic feed material to the temperatures of about 60 to 100° C. The secondary hydrogen production apparatus can include any hydrogen producing apparatus wherein that includes heat. In preferred embodiments, the secondary hydrogen production apparatus is an apparatus that produces hydrogen with by separating H2O into hydrogen or water in one or a series of reactions. In further preferred embodiments, the secondary hydrogen production apparatus is an electrolyzer or a sulfur-iodine system. In one embodiment, a steam based high temperature electrolyzer is combined with the primary hydrogen production apparatus 96 of the invention as shown inFIG. 4 .Electrolyzer 114 includescell 102 having acathode 104 and ananode 106, wherein applied electrical current 112 is applied to the cell. The cell may further include amembrane 108 as needed. Steam andhydrogen stream 110 is conveyed intocell 102, wherein the steam is heated at a temperature from about 100-1000° C. The amount of energy needed as a function of temperature is generally known in the art, as shown in Table 4. The thermal and electro forces will cause a portion of the water or steam to split, wherein oxygen will pass throughion conducting membrane 108 to the anode side and is removed on that side. A mixture of steam and hydrogen, including hydrogen newly formed from separation of the water, exits the cell on the cathode side with heated temperatures. The hydrogen can then be removed from the steam with a condenser. The condenser can function asheat exchanger 12 or can be a separate condenser that functions in tandem withheat exchanger 12. Either way, theheat exchanger 12 obtains heat from the steam that exitscell 102 and uses the heat to dually produce hydrogen in the primary hydrogen production apparatus by elevate the temperature of organic feed material to about 60 to 100° C. - Alternatively, secondary hydrogen production apparatus is a high temperature electrolyzer that uses heated water, as in
FIG. 5 . Here, an electrical current is applied tocathode 116 andanode 118 under heated temperatures of about 100-1000° C., separating a portion of the heated water into oxygen and hydrogen. The oxygen migrates to the anode side acrossdiaphragm 120, while hydrogen migrates to the cathode side.Heat exchanger 12 can obtain heat from the heated water remaining the electrolyzer or by the released, heated oxygen. - In further embodiments, the secondary hydrogen production apparatus is a sulfur-iodide system. In an sulfur-iodine system, sulfuric acid is heated under high temperatures of about 750-1000° C. and low pressure under the reaction H2SO4→H2O+SO2+1/2O2. In certain embodiments, iodine can combine with the resultant sulfur dioxide and water under conditions known in the art under the reaction I2+SO2+2H2O→2HI+H2SO4. The 2HI reacts with water and sulfur dioxide to under temperatures of about 350° C. to produce hydrogen and sulfur dioxide under the reaction 2HI→H2+I2. The net result of the process is the same as electrolysis: 2H2O→2H2+O2. None of the reactions occur with 100 percent efficiency, resulting in super-heated byproducts for
heat exchanger 44 to remove heat from in order to heat organic solution in primary hydrogen production apparatus 96.Heat exchanger 14 can use heat from any heat source from this process, for example, the heated H2SO4, heated H2O or oxygen. Regardless of whereheat exchanger 44 acquires heat, the dual method enables two separate methods of hydrogen production, wherein the primary system uses heat energy from the secondary system in order to treat organic feed material for use inbioreactor 10. - The apparatus combines a bioreactor with a high temperature electrolyzer. The organic feed material is a grape juice waste product diluted in tap water at approximately 32 mL of juice per liter. The solution uses chlorine-free tap water or is aerated previously for 24 hours to substantially remove chlorine. The dilution and aeration occur in a treatment container. The organic feed material is then conveyed into the
heat exchanger 12 through a passage. - The organic feed material is heated in the
heat exchanger 12 to about 65° C. for about 10 minutes to substantially deactivate methanogens. The organic feed material is heated with excess heat from the high temperature electrolyzer with a heat exchanger. The organic feed material is conveyed through a passage to the bioreactor wherein it is further inoculated with Kleibsiella oxytoca. The resultant biogases produced by the microorganisms metabolizing the organic feed material include hydrogen without any substantial methane. - A multiplicity of reactors were initially operated at pH 4.0 and a flow rate of 2.5 mL min−1, resulting in a hydraulic retention time (HRT) of about 13 h (0.55 d). This is equivalent to a dilution rate of 1.8 d−1. After one week all six reactors were at pH 4.0, the ORP ranged from −300 to −450 mV, total gas production averaged 1.6 L d−1 and hydrogen production averaged 0.8 L d−1. The mean COD of the organic feed material during this period was 4,000 mg L−1 and the mean effluent COD was 2,800 mg L−1, for a reduction of 30%. After one week, the pHs of certain reactors were increased by one half unit per day until the six reactors were established at different pH levels ranging from 4.0 to 6.5. Over the next three weeks at the new pH settings, samples were collected and analyzed each weekday. It was found that the optimum for gas production in this embodiment was pH 5.0 at 1.48 L hydrogen d−1 (Table 2). This was equivalent to about 0.75 volumetric units of hydrogen per unit of reactor volume per day.
TABLE 2 Production of hydrogen in 2-L anaerobic bioreactors as a function of pH. Total H2 H2 per gas H2 L/g Sugar pH L/day L/day COD moles/mole 4.0a 1.61 0.82 0.23 1.81 4.5b 2.58 1.34 0.23 1.81 5.0c 2.74 1.48 0.26 2.05 5.5d 1.66 0.92 0.24 1.89 6.0d 2.23 1.43 0.19 1.50 6.5e 0.52 0.31 0.04 0.32
amean of 20 data points
bmean of 14 data points
cmean of 11 data points
dmean of 7 data points
emean of 6 data points
- Also shown in Table 2 is the hydrogen production rate per g of COD, which also peaked at pH 5.0 at a value of 0.26 L g−1 COD consumed. To determine the molar production rate, it was assumed that each liter of hydrogen gas contained 0.041 moles, based on the ideal gas law and a temperature of 25° C. Since most of the nutrient value in the grape juice was simple sugars, predominantly glucose and fructose (Table 1 above), it was assumed that the decrease in COD was due to the metabolism of glucose. Based on the theoretical oxygen demand of glucose (1 mole glucose to 6 moles oxygen), one gram of COD is equivalent to 0.9375 g of glucose. Therefore, using those conversions, the molar H2 production rate as a function of pH ranged from 0.32 to 2.05 moles of H2 per mole of glucose consumed. As described above, the pathway appropriate to these organisms results in two moles of H2 per mole of glucose, which was achieved at pH 5.0. The complete data set is provided in Tables 3a and 3b.
- Samples of biogas were analyzed several times per week from the beginning of the study, initially using a Perkin Elmer Autosystem GC with TCD, and then later with a Perkin Elmer Clarus 500 GC with TCD in series with an FID. Methane was never detected with the TCD, but trace amounts were detected with the FID (as much as about 0.05%).
- Over a ten-day period, the waste solution was mixed with sludge obtained from a methane-producing anaerobic digester at a nearby wastewater treatment plant at a rate of 30 mL of sludge per 20 L of diluted grape juice. There was no observed increase in the concentration of methane during this period. Therefore, it was concluded that the preheating of the feed to 65° C. as described previously was effective in deactivating the organisms contained in the sludge. Hydrogen gas production rate was not affected (data not shown).
- Using this example, hydrogen gas is generated using a microbial culture over a sustained period of time. The optimal pH for this culture consuming simple sugars from a simulated fruit juice bottling wastewater was found to be 5.0. Under these conditions, using plastic packing material to retain microbial biomass, a hydraulic residence time of about 0.5 days resulted in the generation of about 0.75 volumetric units of hydrogen gas per unit volume of reactor per day.
- Whereas particular embodiments of this invention have been described above for purposes of illustration, it will be evident to those skilled in the art that numerous variations of the details of the present invention may be made without departing from the invention as defined in the appended claims.
TABLE 3a Bioreactor Operating Data GAS Total after Liquid Readings collection volume scrubbing Effluent NaOH Net Feed Date Reactor hours (mL) (mL) (mL) (mL) (mL) ORP pH 14-Nov A 5 540 220 780 0 780 −408 4.0 14-Nov B 5 380 220 840 0 840 −413 4.1 14-Nov C 5 350 170 870 0 870 −318 4.1 14-Nov D 5 320 130 920 0 920 −372 4.1 14-Nov E 5 240 100 920 0 920 −324 4.3 14-Nov F 5 50 25 810 0 810 −329 4.0 15-Nov A 5.5 450 230 1120 25 1095 −400 4.0 15-Nov B 5.5 450 235 1180 35 1145 −384 4.0 15-Nov C 5.5 250 130 640 0 640 −278 4.0 15-Nov E 5.5 455 225 1160 0 1160 −435 4.0 15-Nov F 5.5 430 235 1160 0 1160 −312 4.0 16-Nov A 5 380 190 1020 27 993 −414 4.0 5-Dec A 4.5 200 110 500 35 465 −439 4.0 18-Nov A 5 360 190 200 0 200 −423 4.0 21-Nov A 4 320 170 800 40 760 −429 4.0 22-Nov A 3.75 285 190 725 21 704 −432 4.0 29-Nov A 4.25 310 155 750 24 726 −439 4.0 2-Dec A 3.75 250 120 660 26 634 −438 4.0 6-Dec A 3 150 75 540 0 540 −441 4.0 17-Nov A 5.5 300 160 1010 30 980 −414 4.0 averages 4.81 324 164 830 13 817 −392 4.0 16-Nov B 5 400 200 1125 45 1080 −397 4.5 16-Nov D 5 400 165 960 60 900 −360 4.5 16-Nov E 5 490 240 1100 72 1028 −324 4.5 1-Dec B 3.5 500 260 570 45 525 −415 4.5 6-Dec B 3 470 240 650 40 610 −411 4.5 21-Nov B 4 560 300 930 50 880 −397 4.5 2-Dec B 3.75 640 320 830 50 780 −407 4.5 17-Nov B 5.5 450 220 1165 50 1115 −406 4.5 18-Nov B 5 390 220 860 42 818 −406 4.5 22-Nov B 3.75 585 395 835 50 785 −397 4.5 29-Nov B 4.25 620 320 920 42 878 −410 4.5 5-Dec B 4.5 390 190 750 37 713 −417 4.5 16-Nov F 5 400 200 1082 93 989 −324 4.5 16-Nov C 5 400 200 950 74 876 −325 4.6 averages 4.45 478 248 909 54 856 −385 4.5 COD Performance Feed Effluent Removal Loading Consumed Total gas H2 H2 Date (mg/L) (mg/L) (mg/L) (g) (g) L/day L/day L/g COD 14-Nov 4,480 2,293 2,187 3.494 1.706 2.59 1.06 0.13 14-Nov 4,480 2,453 2,027 3.763 1.702 1.82 1.06 0.13 14-Nov 4,480 2,293 2,187 3.898 1.902 1.68 0.82 0.09 14-Nov 4,480 1,920 2,560 4.122 2.355 1.54 0.62 0.06 14-Nov 4,480 2,773 1,707 4.122 1.570 1.15 0.48 0.06 14-Nov 3,307 2,080 1,227 2.679 0.994 0.24 0.12 0.03 15-Nov 3,307 3,787 (480) 3.621 −0.525 1.96 1.00 −0.44 15-Nov 3,307 3,253 54 3.787 0.061 1.96 1.03 3.82 15-Nov 3,307 3,520 (213) 2.116 −0.138 1.09 0.57 −0.95 15-Nov 3,307 3,467 (160) 3.836 −0.165 1.99 0.98 −1.21 15-Nov 3,307 3,413 (106) 3.836 −0.123 1.88 1.03 −1.91 16-Nov 4,693 3,627 1,066 4.660 1.059 1.82 0.91 0.18 5-Dec 4,267 4,160 107 1.984 0.050 1.07 0.59 2.21 18-Nov 3,680 5,227 (1,547) 0.736 −0.309 1.73 0.91 −0.61 21-Nov 3,493 3,680 (187) 2.655 −0.142 1.92 1.02 −1.20 22-Nov 4,107 2,293 1,813 2.891 1.277 1.82 1.22 0.15 29-Nov 5,013 3,520 1,493 3.640 1.084 1.75 0.88 0.14 2-Dec 4,587 3,893 694 2.908 0.440 1.60 0.77 0.27 6-Dec 4,853 3,093 1,760 2.621 0.950 1.20 0.60 0.08 17-Nov 4,907 3,520 1,387 4.809 1.359 1.31 0.70 0.12 averages 4,092 3,213 879 3.344 0.718 1.61 0.82 0.23 16-Nov 4,693 3,520 1,173 5.068 1.267 1.92 0.96 0.16 16-Nov 4,693 3,573 1,120 4.224 1.008 1.92 0.79 0.16 16-Nov 4,693 3,413 1,280 4.824 1.315 2.35 1.15 0.18 1-Dec 5,173 3,680 1,493 2.716 0.784 3.43 1.78 0.33 6-Dec 4,853 3,360 1,493 2.960 0.911 3.76 1.92 0.26 21-Nov 3,493 3,147 346 3.074 0.305 3.36 1.80 0.98 2-Dec 4,587 3,413 1,174 3.578 0.915 4.10 2.05 0.35 17-Nov 4,907 2,933 1,974 5.471 2.201 1.96 0.96 0.10 18-Nov 3,680 2,960 720 3.010 0.589 1.87 1.06 0.37 22-Nov 4,107 2,720 1,387 3.224 1.089 3.74 2.53 0.36 29-Nov 5,013 3,307 1,707 4.402 1.498 3.50 1.81 0.21 5-Dec 4,267 3,840 427 3.042 0.304 2.08 1.01 0.62 16-Nov 4,693 3,093 1,600 4.641 1.582 1.92 0.96 0.13 16-Nov 4,693 2,933 1,760 4.111 1.541 1.92 0.96 0.13 averages 4,539 3,278 1,261 3.883 1.079 2.58 1.34 0.23 -
TABLE 3b Bioreactor Operating Data Continued GAS Total after Liquid Readings collection volume scrubbing Effluent NaOH Net Feed Date Reactor hours (mL) (mL) (mL) (mL) (mL) ORP pH 17-Nov C 5.5 360 200 840 120 720 −344 4.9 18-Nov C 5 370 200 1120 70 1050 −328 4.9 29-Nov C 4.25 415 200 920 50 870 −403 4.9 17-Nov E 5.5 490 270 1210 115 1095 −352 5.0 1-Dec D 3.5 540 250 710 85 625 −395 5.0 17-Nov F 5.5 475 225 1120 130 990 −367 5.0 5-Dec D 4.5 580 310 710 77 633 −423 5.0 6-Dec D 3 450 240 490 43 447 −420 5.0 17-Nov D 3.5 680 415 580 83 497 −326 5.0 2-Dec D 3.75 640 340 830 66 764 −412 5.0 22-Nov C 3.75 460 295 800 50 750 −349 5.0 averages 4.34 496 268 848 81 767 −374.5 5.0 5-Dec C 4.5 470 250 900 103 797 −429 5.4 18-Nov F 5 90 45 600 55 545 −451 5.5 21-Nov D 4 130 70 830 80 750 −454 5.5 22-Nov D 3.75 360 250 765 69 696 −461 5.5 29-Nov D 4.25 100 50 940 100 840 −456 5.5 2-Dec C 3.75 550 290 810 93 717 −430 5.5 6-Dec C 3 250 130 570 45 525 −428 5.5 averages 4.04 279 155 774 78 696 −444.1 5.5 21-Nov E 4 350 250 930 130 800 −400 6.0 22-Nov E 3.75 380 280 820 127 693 −411 6.0 29-Nov E 4.25 360 230 870 71 799 −467 6.0 1-Dec E 3.5 420 250 770 127 643 −471 6.0 2-Dec E 3.75 280 170 540 85 455 −443 6.0 5-Dec E 4.5 410 240 930 156 774 −487 6.0 6-Dec E 3 280 170 660 105 555 −490 6.0 averages 3.82 354 227 789 114 674 −453 6.0 29-Nov F 4.25 90 45 870 150 720 −501 6.5 2-Dec F 3.75 20 0 810 136 674 −497 6.5 22-Nov F 3.75 120 105 790 128 662 −477 6.5 5-Dec F 4.5 10 0 670 121 549 −532 6.5 6-Dec F 3 60 50 480 90 390 −515 6.5 21-Nov F 4 200 100 910 150 760 −472 6.5 averages 3.88 83 50 755 129 626 −499 6.5 COD Performance Feed Effluent Removal Loading Consumed Total gas H2 H2 Date (mg/L) (mg/L) (mg/L) (g) (g) L/day L/day L/g COD 17-Nov 4,907 2,880 2,027 3.533 1.459 1.57 0.87 0.14 18-Nov 3,680 2,480 1,200 3.864 1.260 1.78 0.96 0.16 29-Nov 5,013 3,093 1,920 4.362 1.670 2.34 1.13 0.12 17-Nov 4,907 4,747 160 5.373 0.175 2.14 1.18 1.54 1-Dec 5,173 3,573 1,600 3.233 1.000 3.70 1.71 0.25 17-Nov 4,907 3,760 1,147 4.858 1.135 2.07 0.98 0.20 5-Dec 4,267 3,573 694 2.701 0.439 3.09 1.65 0.71 6-Dec 4,853 3,253 1,600 2.169 0.715 3.60 1.92 0.34 17-Nov 4,907 4,213 694 2.439 0.345 4.66 2.85 1.20 2-Dec 4,587 3,787 800 3.504 0.611 4.10 2.18 0.56 22-Nov 4,107 1,280 2,827 3.080 2.120 2.94 1.89 0.14 averages 4,664 3,331 1,333 3.579 1.023 2.74 1.48 0.26 5-Dec 4,267 3,413 854 3.401 0.680 2.51 1.33 0.37 18-Nov 3,680 3,440 240 2.006 0.131 0.43 0.22 0.34 21-Nov 3,493 3,360 133 2.620 0.100 0.78 0.42 0.70 22-Nov 4,107 2,880 1,227 2.858 0.854 2.30 1.60 0.29 29-Nov 5,013 3,307 1,707 4.211 1.434 0.56 0.28 0.03 2-Dec 4,587 3,573 1,014 3.289 0.727 3.52 1.86 0.40 6-Dec 4,853 3,627 1,226 2.548 0.644 2.00 1.04 0.20 averages 4,286 3,371 914 2.982 0.636 1.66 0.92 0.24 21-Nov 3,493 2,987 506 2.794 0.405 2.10 1.50 0.62 22-Nov 4,107 2,453 1,653 2.846 1.146 2.43 1.79 0.24 29-Nov 5,013 1,973 3,040 4.006 2.429 2.03 1.30 0.09 1-Dec 5,173 2,933 2,240 3.326 1.440 2.88 1.71 0.17 2-Dec 4,587 3,360 1,227 2.087 0.558 1.79 1.09 0.30 5-Dec 4,267 3,253 1,014 3.303 0.785 2.19 1.28 0.31 6-Dec 4,853 2,293 2,560 2.693 1.421 2.24 1.36 0.12 averages 4,499 2,750 1,749 3.033 1.179 2.23 1.43 0.19 29-Nov 5,013 1,707 3,307 3.610 2.381 0.51 0.25 0.02 2-Dec 4,587 3,573 1,014 3.092 0.683 0.13 0.00 0.00 22-Nov 4,107 2,240 1,867 2.719 1.236 0.77 0.67 0.08 5-Dec 4,267 2,827 1,440 2.343 0.791 0.05 0.00 0.00 6-Dec 4,853 2,240 2,613 1.893 1.019 0.48 0.40 0.05 21-Nov 3,493 2,613 880 2.655 0.669 1.20 0.60 0.15 averages 4,387 2,533 1,853 2.745 1.160 0.52 0.31 0.04 -
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Claims (16)
1. An apparatus for dually producing hydrogen, comprising:
a secondary hydrogen production apparatus including an apparatus that breaks down chemical compounds, wherein hydrogen is produced from one or a series of reactions using heated liquids, vapors or gases,
a primary hydrogen production apparatus operably combined with the secondary hydrogen production apparatus, the primary hydrogen production apparatus including a bioreactor adapted to produce hydrogen from microorganisms metabolizing an organic feed material, and
a heat exchanger operably associated with the primary and secondary hydrogen production apparatuses such that heat from the secondary hydrogen production apparatus is transferred to the primary hydrogen production apparatus.
2. The apparatus of claim 1 , wherein the heated liquids, vapors and gases are selected from the group comprising of water, steam, hydrochloric acid, oxygen and sulfur dioxide.
3. The apparatus of claim 1 , wherein the heated liquids, vapors and gases in the secondary hydrogen production apparatus are at a temperature in a range of about 100 to 1000° C.
4. The apparatus of claim 1 , wherein the organic feed material is heated for a period of at least fifteen minutes.
5. The apparatus of claim 1 , wherein the organic feed material is heated by the heat to a temperature of about 60 to 100° C.
6. The apparatus of claim 1 , wherein the organic feed material in the bioreactor has a controlled pH by a pH controlling device.
7. The apparatus of claim 1 , wherein the secondary hydrogen production apparatus is a steam based high temperature electrolyzer.
8. The apparatus of claim 1 , wherein the secondary hydrogen production apparatus is a water based high temperature electrolyzer.
9. The apparatus of claim 1 , wherein the secondary hydrogen production apparatus is an apparatus conducive to sulfur iodide processes.
10. The apparatus of claim 1 , wherein the heat-exchanger is a gas/liquid heat exchanger.
11. The apparatus of claim 1 wherein the heat-exchanger is a liquid/liquid heat exchanger.
12. The apparatus of claim 1 , wherein the primary hydrogen production apparatus further comprises a passage providing entry access to the bioreactor and providing removal access to the heat exchanger.
13. The apparatus of claim 12 , further providing treatment means for treating an organic feed material contained within the primary hydrogen production apparatus.
14. The apparatus of claim 12 , further comprising an electronic controller having at least one microprocessor adapted to process signals from a one or a plurality of devices providing organic feed material parameter information, wherein the electronic controller is connected to the at least one actuatable terminal and is arranged to control the operation of the heat exchanger and the temperature of any contents therein.
15. The apparatus of claim 12 , further comprising a pump operably related to the passage.
16. An apparatus for dually producing hydrogen, comprising:
a secondary hydrogen production apparatus including an electrolyzer, wherein hydrogen is produced from one or a series of reactions using heated liquids, vapors or gases,
a primary hydrogen production apparatus operably combined with the secondary hydrogen production apparatus, the primary hydrogen production apparatus including a bioreactor adapted to produce hydrogen from microorganisms metabolizing an organic feed material, and
a heat exchanger operably associated with the primary and secondary hydrogen production apparatuses such that heat from the secondary hydrogen production apparatus is transferred to the primary hydrogen production apparatus.
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