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WO2011070624A1 - Method of organic-waste modification accompanied by generation of high-concentration hydrogen gas and device for modifying organic waste - Google Patents

Method of organic-waste modification accompanied by generation of high-concentration hydrogen gas and device for modifying organic waste Download PDF

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Publication number
WO2011070624A1
WO2011070624A1 PCT/JP2009/006784 JP2009006784W WO2011070624A1 WO 2011070624 A1 WO2011070624 A1 WO 2011070624A1 JP 2009006784 W JP2009006784 W JP 2009006784W WO 2011070624 A1 WO2011070624 A1 WO 2011070624A1
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Prior art keywords
reforming
organic waste
reaction
container
water
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Ceased
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PCT/JP2009/006784
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French (fr)
Japanese (ja)
Inventor
山田廣美
祥雲弘文
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RE SCIENCESYSTEM Corp
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RE SCIENCESYSTEM Corp
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Priority to PCT/JP2009/006784 priority Critical patent/WO2011070624A1/en
Publication of WO2011070624A1 publication Critical patent/WO2011070624A1/en
Anticipated expiration legal-status Critical
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B09DISPOSAL OF SOLID WASTE; RECLAMATION OF CONTAMINATED SOIL
    • B09BDISPOSAL OF SOLID WASTE NOT OTHERWISE PROVIDED FOR
    • B09B3/00Destroying solid waste or transforming solid waste into something useful or harmless
    • B09B3/70Chemical treatment, e.g. pH adjustment or oxidation
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/02Fixed-bed gasification of lump fuel
    • C10J3/20Apparatus; Plants
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72Other features
    • C10J3/723Controlling or regulating the gasification process
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J3/00Production of combustible gases containing carbon monoxide from solid carbonaceous fuels
    • C10J3/72Other features
    • C10J3/82Gas withdrawal means
    • C10J3/84Gas withdrawal means with means for removing dust or tar from the gas
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10KPURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
    • C10K1/00Purifying combustible gases containing carbon monoxide
    • C10K1/02Dust removal
    • C10K1/024Dust removal by filtration
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0211Processes for making hydrogen or synthesis gas containing a reforming step containing a non-catalytic reforming step
    • C01B2203/0216Processes for making hydrogen or synthesis gas containing a reforming step containing a non-catalytic reforming step containing a non-catalytic steam reforming step
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/025Processes for making hydrogen or synthesis gas containing a partial oxidation step
    • C01B2203/0255Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a non-catalytic partial oxidation step
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205Composition of the feed
    • C01B2203/1211Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235Hydrocarbons
    • C01B2203/1247Higher hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913Carbonaceous raw material
    • C10J2300/0916Biomass
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0913Carbonaceous raw material
    • C10J2300/0946Waste, e.g. MSW, tires, glass, tar sand, peat, paper, lignite, oil shale
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0956Air or oxygen enriched air
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/09Details of the feed, e.g. feeding of spent catalyst, inert gas or halogens
    • C10J2300/0953Gasifying agents
    • C10J2300/0973Water
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10JPRODUCTION OF PRODUCER GAS, WATER-GAS, SYNTHESIS GAS FROM SOLID CARBONACEOUS MATERIAL, OR MIXTURES CONTAINING THESE GASES; CARBURETTING AIR OR OTHER GASES
    • C10J2300/00Details of gasification processes
    • C10J2300/18Details of the gasification process, e.g. loops, autothermal operation
    • C10J2300/183Non-continuous or semi-continuous processes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/141Feedstock
    • Y02P20/145Feedstock the feedstock being materials of biological origin

Definitions

  • the present invention provides a method of reforming organic waste accompanied by generation of high concentration hydrogen gas, and an apparatus for reforming organic waste for realizing the method of reforming the waste.
  • Steam reforming is a method of anaerobically reacting hydrocarbons with high temperature steam at around 1000 ° C. to convert them into hydrogen gas, methane, carbon monoxide and other low molecular weight gases.
  • a typical example is steam reforming of methane, which is extremely important industrially as the only method for mass production of hydrogen gas with high demand for fuel cell and ammonia production by the Harbor Bosch method ( Below).
  • Patent Document 1 discloses a gasification and reforming method of waste that gasifies waste such as municipal waste and industrial waste and recovers the resulting gas as a gas for fuel and the like.
  • Patent Document 2 proposes a method for treating waste and a method and apparatus for recovering pyrolysis gas, in order to obtain new energy by effectively using industrial waste and general waste.
  • Patent Document 3 is capable of quickly and sufficiently reforming hydrocarbon fuels such as gasoline and light oil even at relatively low temperature conditions of 400 ° C. or less, and has a small amount of carbon monoxide and methane by-products, and is compact without receiving nitrogen dilution.
  • hydrocarbon fuels such as gasoline and light oil
  • Patent Document 3 Disclosed are a fuel reforming system and a hydrogen rich gas producing method.
  • Patent Document 1 wastes such as urban waste and industrial waste accumulated in pits are compressed with a press before hydrogen recovery, and heated to reflux in the drying and pyrolysis step, and as high as 1200 ° C. In the process of reforming at the same time, it is necessary to go through complicated processes while consuming a large amount of energy.
  • Patent Document 2 requires a large amount of energy, such as partially burning a part of the pyrolysis gas generated in the pyrolysis furnace to a high temperature of 1000 ° C. or more, in order to convert waste into energy.
  • the heat-resistant structuring of the reforming furnace becomes indispensable, which causes a problem that the cost of the apparatus itself is increased.
  • Patent Document 3 it is not easy to deploy a fuel reforming system for a fuel cell, the cost for providing a necessary material such as a reforming catalyst, supercritical water or subcritical water, and system operation time Energy consumption and other problems.
  • the present invention has an object to solve the above-mentioned problems, and relates to a technology for taking out the energy contained in organic waste by a simple method and converting it into a highly useful form such as hydrogen gas.
  • the reforming reaction according to the present invention requires only external water supply, and high temperature steam as high as 1000 ° C. and an expensive precious metal catalyst are unnecessary. Furthermore, it is possible to modify organic waste in a very environmentally friendly manner without the use of external energy.
  • the present invention provides a method of reforming organic waste without using external energy, and an organic waste reforming apparatus for realizing the reforming method. In addition, high concentration hydrogen gas generated by reforming organic waste can be recovered and used.
  • the method for reforming organic waste according to claim 1 is A reaction initiation step of feeding organic waste into a reforming vessel and initiating reforming of a portion of the organic waste using a reaction initiator; A reaction expansion step of expanding the reaction by aeration into the reforming container with a gas introduction pipe and water supply for performing a combustion reaction with water; A steady-state reaction step in which reforming is performed in a steady manner by maintaining the size of combustion nuclei; And is accompanied by the generation of high concentration hydrogen gas.
  • reaction initiation step according to claim 1 uses a small amount of carbide and water as the reaction initiator to ignite a portion of the organic waste. And a step of
  • aeration into the reforming container in the reaction expansion step according to claim 1 or 2 is the introduction of outside air into the reforming container by the gas introducing pipe. It is characterized by adjusting.
  • the water supply in the reaction expansion step according to claims 1 to 3 is characterized in that water is continuously replenished from the outside by a water supply means.
  • the maintenance of the size of the combustion nuclei in the reaction steady process according to claims 1 to 4 is the gas based on temperature detection using a temperature sensor. It is characterized in that it is performed by aeration into the reforming container by the introduction pipe and adjusting the water supply into the reforming container.
  • the apparatus for reforming organic waste is Means for supplying organic waste, A reforming vessel for reforming organic waste supplied from the supply means; A temperature sensor for grasping the temperature condition during combustion of organic waste, A gas introduction pipe for ventilating the inside of the reforming container, a water supply means for replenishing water for reforming, and An exhausting means for discharging the reformed reforming residue to the outside; Exhaust gas processing means for processing the gas discharged from the reforming container; And is accompanied by the generation of high concentration hydrogen gas.
  • reforming in the method for reforming organic waste of the present invention, reforming can be continuously performed without using external energy in the reaction steady process. Further, the gas generated by the reforming contains high concentration hydrogen, which can be recovered and used as hydrogen gas.
  • the reaction initiation step includes the step of igniting part of the organic waste using a small amount of carbide and water as the reaction initiator. Reforming can be initiated with minimal energy.
  • aeration into the reforming container is characterized by adjusting the introduction of the outside air into the reforming container by the gas introduction pipe, so that in the reforming, It can be carried out extremely easily without stopping the continuous reaction.
  • the water supply in the reaction expansion step is characterized by continuously replenishing water from the outside by the water supply means, without using external energy such as a combustion agent, It can be reformed.
  • the maintenance of the size of the combustion nucleus in the reaction steady process is based on the temperature detection using the temperature sensor, the aeration into the reforming container by the gas introducing pipe, and Since the adjustment is performed by adjusting the water supply into the reforming container, it is possible to accurately sense and maintain the change in size of the combustion core.
  • the apparatus for reforming organic waste according to the present invention can maintain a sealed state in the reforming process and has exhaust gas treatment means, so that odor and other harmful gases do not leak to the outside.
  • exhaust gas treatment means so that odor and other harmful gases do not leak to the outside.
  • a large amount of organic waste can be reformed by simple equipment.
  • An apparatus can be provided.
  • the method for reforming organic waste of the present invention will be described.
  • the reforming process is divided into three stages. That is, a reaction start step of supplying organic waste into the reforming container and starting reforming in a part of the organic waste using the reaction initiator, aeration into the reforming container by the gas introduction pipe,
  • the reaction expansion step is a reaction expansion step in which the reaction is expanded by water supply for carrying out a combustion reaction with water, and the reaction steady step in which reforming is performed in a steady manner by maintaining the size of the combustion core.
  • a reaction start step a predetermined amount of organic waste is supplied into the reforming container, and a reaction initiator is used to ignite a part of the organic waste to start the reaction.
  • a reaction initiator organic waste is ignited by using a small amount of carbide and water.
  • the reforming container is filled with air containing oxygen, and acetylene gas is generated by the reaction of the carbide and water, so that the organic waste is also ignited instantaneously by igniting this acetylene.
  • acetylene gas is generated by the reaction of the carbide and water, so that the organic waste is also ignited instantaneously by igniting this acetylene.
  • a predetermined amount of water is added before reaction start.
  • the reaction site in the input organic waste is expanded by aeration into the reforming container by the gas introduction pipe and water supply for performing the combustion reaction with water.
  • the combustion reaction using oxygen is continuously occurring.
  • the combustion reaction using oxygen raises the temperature of the surrounding organic waste and the water contained therein, causing the reaction between the organic waste and water, that is, the water combustion reaction.
  • the ventilation into the reforming container by the gas introduction pipe can change the ventilation state by moving the tip of the gas introduction pipe from the center of the reforming container to the periphery, and oxygen was used. The combustion reaction spreads from the organic waste center to the periphery.
  • the combustion reaction using this oxygen further generates heat, and the combustion reaction by water in the organic waste is expanded.
  • This series of reactions can expand the reaction in the organic waste in the reaction expansion step.
  • the combustion reaction by oxygen is suppressed to such an extent that it does not spread to the whole organic waste.
  • the presence of the organic waste in the reforming vessel and the combustion products generated by the combustion reaction with oxygen prevent the aeration state from occurring to a small extent at the reaction site in the organic waste. The reaction is suppressed to the extent that it does not spread throughout the organic waste.
  • the combustion reaction by water in the organic waste will be described.
  • the combustion reaction in a narrow sense refers to a violent oxidation reaction involving heat and light due to oxygen.
  • this is expressed by a chemical reaction formula, it is approximately as shown in FIGS. 7 (a) and 7 (b). That is, assuming that organic wastes such as biomass are carbohydrates (FIG. 7 (a)) or hydrocarbons (FIG. 7 (b)), carbon dioxide and water are produced after reaction with oxygen.
  • the combustion reaction with water in the present invention is a reaction using water as an oxidant to generate hydrogen from carbohydrates or hydrocarbons. If this is represented by a chemical reaction formula, it will become like FIG. 7 (c) (d).
  • the reaction steady state is formed by returning the gas introduction pipe from the inner peripheral portion to the central portion of the reforming container when all the temperature sensors installed in the reforming container detect the temperature rise.
  • the high temperature part of the organic waste core at this time is called a combustion core, and this state is called a reaction steady process.
  • the temperature around the combustion core is about 150 to 200 ° C.
  • the gas phase in the reforming vessel is about 80 ° C.
  • the outside of the reforming vessel is about 40 ° C.
  • oxygen is moved by moving the tip end of the gas introduction pipe of the gas introduction pipe installed in the peripheral wall of the reforming container from the center of the reforming container to the periphery as in the reaction expansion step. It is possible to expand the combustion reaction by and repeat the reforming step from the reaction expansion step again. Also in this case, it is not necessary to use external energy, and the reaction can be expanded by aeration into the reforming container with a gas introduction pipe and water supply for performing a combustion reaction with water, leading to a reaction steady process. It is possible. In addition, when the combustion nuclei are expanded too much, it is possible to adjust the combustion reaction by oxygen by reducing the amount of aeration through the gas introduction pipe.
  • the organic waste is used as the reforming container It is supplied to the inside and left for several hours until all the temperature sensors installed in the reforming container detect the temperature rise.
  • the gas introduction pipe is returned from the inner peripheral portion to the central portion of the reforming container and water is supplied into the reforming container to continue the reaction steady process.
  • the three-stage reforming process makes it possible to reform organic waste without external energy supply.
  • the hydrogen concentration of the exhaust gas may be detected, and water may be supplied when the hydrogen concentration falls below 2%, for example.
  • organic waste is assumed to be organic waste including natural and synthetic organic waste such as garbage, waste paper, biomass such as grass, rubber and plastics etc. Not limited to these.
  • the apparatus for reforming organic waste comprises an organic waste supply means, a reforming container for reforming the organic waste supplied from the supply means, and a temperature state during combustion of the organic waste. Temperature sensor for grasping the gas, a gas introduction pipe for ventilating the inside of the reforming container, water supply means for replenishing water for reforming, and the reforming residue subjected to reforming to the outside It has the discharge
  • the means for supplying organic waste in the apparatus for reforming organic waste according to the present invention comprises a supply port and a supply port cover.
  • the supply port is formed in such a manner as to open to the reformer container ceiling, and supply of organic waste is performed. By providing the supply port at the ceiling, it is possible to uniformly supply the organic waste into the reforming container.
  • the reforming container comprises a container wall and a leg.
  • the container wall comprises a flat regular hexagonal ceiling, a peripheral wall provided below the outer peripheral edge of the ceiling, and a flat regular hexagonal bottom similar to the ceiling.
  • the peripheral wall portion is preferably formed of a fire-resistant wall portion and an outer wall portion covering the fire-resistant wall portion.
  • the peripheral wall portion is simply formed of a generally used steel plate.
  • the steel plate preferably has a thickness of about 10 cm.
  • a plurality of leg portions are attached to the lower end portion of the peripheral wall portion, and the reforming container can be installed at a certain height from the ground by being formed with the same length of about 50 cm.
  • the reforming container can be held horizontally by adjusting the length of the legs.
  • the reforming container is a container having a volume of about 1000 liters, a regular hexagonal shape of about 60 cm on one side of the bottom and the ceiling, and a regular hexagonal column shape having a height of about 1 m from the bottom to the ceiling. Is not limited to this. Further, the shape is not limited to a regular hexagonal column shape, and may be a cylindrical shape or the like.
  • a plurality of temperature sensors for grasping the temperature state during combustion of the organic waste are installed in the reforming container, and the temperature detection portion is projected from the outer wall portion of the reforming container into the inside of the reforming container, The temperature of the organic waste during combustion in the reforming vessel is detected.
  • the temperature sensor serves to measure the size of combustion nuclei in the organic waste being burned.
  • the temperature sensor has a cylindrical shape with a diameter of about 1 to 5 cm and a total length of about 50 cm, and comprises a temperature detection portion, a main body, and a display portion. Protruding into the reforming vessel, the temperature detection site can detect the temperature of the organic waste being burned.
  • the drilling holes are located at a height of about 50 cm from the bottom of the reforming container, and when the reforming container has a regular hexagonal column shape, a total of six holes, one each from the six side portions of the reforming container
  • the temperature sensor in the reforming vessel is used to sense the temperature in the reforming vessel, and the temperature sensing portion of each temperature sensor is arranged in a circle with a radius of about 15 cm from the center of the vessel in the reforming vessel. In the reaction steady process, when the temperature of at least one of the temperature sensors is less than 200 ° C.
  • the tip end of the gas introduction pipe of the gas introduction pipe is moved from the center of the reforming container to the periphery Then, the combustion reaction can be continuously performed by expanding the size of the combustion nucleus in the organic waste and supplying water from the water supply means into the reforming container.
  • the temperature detected by the temperature detection part can be confirmed by the display unit.
  • the gas introducing pipe for ventilating the inside of the reforming container is a metal pipe having a diameter of about 3 cm and a total length of about 60 cm, and is installed on a peripheral wall of the reforming container. Since outside air is always introduced from the tip of the gas introduction pipe, the combustion reaction by oxygen is constantly occurring at a constant rate in the reforming container.
  • the gas introduction pipe is located at a height of about 20 cm from the lower end of the reforming container, and through the holes bored in the center of each side of the peripheral wall of the reforming container, the outside air is introduced into the reforming container from the outside of the reforming container. Introduce.
  • the gas introduction pipe can be moved, and the vent position can be adjusted in the reforming container without being fixed in position. Further, in order to increase the amount of air flow into the reforming container, it is possible to form a small hole on the side of the gas introduction pipe.
  • a water supply means for replenishing water for reforming includes a water supply tank and a shower portion for supplying water to the organic waste being burned in the reforming container.
  • the water supply tank is provided at the center of the ceiling of the reforming container, and can be constantly stored in the water supply tank.
  • the water supply tank and the shower unit are separated by a lower cover of the water supply tank, and water can be sent from the inside of the water supply tank to the shower unit as needed.
  • a large number of holes are opened in the shower head of the shower section, and the structure is such that water is evenly distributed to the entire organic waste during combustion inside the reforming container by spraying water.
  • the showerhead has a spherical shape, but is not limited thereto.
  • the water supply amount at one time it is preferable to adjust the water supply amount at one time so that the total amount of the water content of the organic waste and the water supply amount does not exceed the weight of the organic waste. Moreover, in order to supply water simply, it is also possible to open the supply port of organic waste and to supply water.
  • the discharging means for discharging the reformed reforming residue to the outside takes out the reforming residue accumulated inside from the exhaust port installed in the reforming container peripheral wall portion.
  • the organic waste is reformed, and the generated reforming residue accumulates near the outlet.
  • a plurality of discharge ports can be installed in the reforming container peripheral wall portion. With regard to recovery of the reforming residue, the reforming residue is removed at a rate of about once every two days because the volume reduction rate is large in the formation of the reforming residue from the organic waste.
  • the reformed residue taken out can be used as fertilizer depending on the type of organic waste.
  • the position of the discharge port is not limited to this, and the discharge port can also be installed at the bottom of the reforming container.
  • the exhaust gas processing means for processing the gas discharged from the reforming container comprises a vent cylinder, a gas collecting portion, a tar removing portion and a suction fan.
  • the aeration cylinder is provided outside the peripheral wall of the reforming container, and the gas generated by the modification is forced to be sucked by the suction fan to flow into the aeration cylinder and pass through the aeration cylinder.
  • Useful gas is collected in the collection section.
  • hydrogen gas useful in the reforming step is generated at a high concentration, so the hydrogen gas is collected in the gas collection unit, but the present invention is limited thereto It is possible to change the collection means according to the necessary gas appropriately in the gas collection unit.
  • the gas collection portion can be installed by forming a through hole in the top of the reforming container, and hydrogen can be collected directly from the inside of the reforming container.
  • the tar removing unit by laying wood pellets made of sawdust or the like or activated carbon, it can play the role of a filter, and it is possible to purify the gas finally discharged.
  • the high concentration hydrogen gas generated by the reforming is collected by, for example, a hydrogen storage alloy in the gas collection unit, but the hydrogen recovery method is not limited thereto, and a known hydrogen recovery means can be used. .
  • a hydrogen sensor or a gas analyzer that simultaneously detects the hydrogen concentration may be provided.
  • a pressure gauge in the reforming container and measure the pressure in the reforming container in the reforming step to adjust the suction by the suction fan so that the reduced pressure state in the container can be maintained.
  • FIG. 1 is a flow chart of the organic waste reforming process of the present invention.
  • the reforming process is divided into three stages. That is, a reaction start step S1 of supplying organic waste into the reforming container and starting reforming in a part of the organic waste using the reaction initiator, reforming in the reforming container by the gas introduction pipe
  • the reaction expansion step S2 is a reaction expansion step S2 in which the reaction is expanded by aeration in the container and water supply for performing a combustion reaction with water, and a reaction steady step S3 in which reforming is performed in a steady manner by maintaining the size of the combustion core.
  • the reaction expansion step S2 is continued for about 600 minutes, and then the reaction steady step S3 is performed.
  • the reaction expansion process S2 is repeated again to form the combustion nucleus.
  • the combustion using oxygen is performed by moving the gas introduction pipe to the inner peripheral portion of the reforming container.
  • the reaction steady process S3 is maintained by expanding the reaction and returning the gas introduction pipe to the central portion inside the reforming container when all the temperature sensors detect 200.degree. If temperature rise is not recognized even if the gas introduction pipe is moved to the inner peripheral part of the reforming container, organic waste is supplied, and if temperature rise is observed, the gas introduction pipe is modified in the same manner as above.
  • the reaction steady process S3 is maintained. If the temperature rise is not recognized even if the organic waste is supplied, the organic waste is further supplied.
  • water is supplied to continue the combustion reaction, but for the timing of supplying water, the hydrogen concentration of the exhaust gas is detected, and the hydrogen concentration is Water may be supplied when it falls below 2%.
  • the organic waste reforming apparatus 10 grasps the temperature condition of the organic waste 15 during combustion and the reforming container 11 for reforming the organic waste 15 supplied from the supply means 13. Temperature sensor 22, a gas introduction pipe 23 for ventilating the inside of the reforming container 18, water supply means 20 for replenishing water for reforming, and a reforming residue 17 for which reforming is performed And an exhaust gas processing means 21 for processing the gas discharged from the reforming container 11.
  • the supply means 13 includes a supply port 13a for receiving the organic waste and supplying the organic waste to the inside 18 of the reforming container 11, and a supply port cover 13b fitted to the supply port 13a.
  • the reforming container 11 for reforming organic waste is composed of a container wall 12 including a ceiling 12a, a peripheral wall 12b, and a bottom 12c, and a leg 16.
  • the reforming container 11 is a container having a regular hexagonal column shape, and is a container having a volume of 1000 liters and having a regular hexagon of about 60 cm on one side and a total height of about 1 m.
  • the six leg portions 16 are installed at the bottom portion 12c and have the same length of about 50 cm, so that the reforming container 11 can be installed at a certain height from the ground. Further, when the installation point is inclined, the reforming container 11 can be held horizontally by adjusting the length of the leg portion 16.
  • rice husk is used as about 30 kg of organic waste 15, and after the organic waste 15 is supplied from the supply means 13 to the reforming container 11, a reaction is performed using a small amount of carbide and water.
  • the organic waste 15 is ignited.
  • the reaction site is expanded by aeration into the reforming container 18 by the gas introduction pipe 23 and water supply for performing a combustion reaction with water.
  • the tip end of the gas introduction pipe 23 is moved from the central portion of the reforming container 11 to the peripheral portion to expand the combustion reaction using oxygen from the central portion of the organic waste 15 to the peripheral portion.
  • the reaction steady state is formed by returning the tip portion of the gas introduction pipe 23 from the inner peripheral portion of the reforming container 11 to the central portion.
  • a combustion nucleus 24 is formed in the high temperature portion of the central portion of the organic waste 15.
  • the combustion nucleus 24 is formed in the center of the organic waste 15 in the form of a sphere having a diameter of about 30 cm, and maintains a substantially constant size in the reaction steady process S3.
  • the temperature of the combustion core peripheral portion 25 is around 180 ° C., around 80 ° C. in the reforming vessel 18 and around 40 ° C.
  • the organic waste 15 is additionally supplied to the inside of the reforming container 18 by about 5 kg. Further, by continuously supplying water to the organic waste 15 by the water supply means 20, the stop of the combustion reaction due to the lack of water is prevented. At this time, the amount of water supplied is adjusted so that the amount of water supplied once does not exceed the dry weight of the input organic waste.
  • the temperature sensor 22 has a cylindrical shape with a diameter of 5 cm and a total length of about 50 cm, and comprises a temperature detection portion 22a, a main body 22b, and a display portion 22c.
  • a temperature detection portion 22 a protrudes from the provided drilling hole 14 into the reforming container 18, and detects the temperature of the organic waste 15 during combustion.
  • the temperature detection portion 22 a can detect the temperature within a range of about 5 cm from the tip of the temperature sensor 22.
  • the drilled hole 14 is located at a height of about 50 cm from the bottom of the reforming container 12c, and the temperature detection portion 22a of each temperature sensor 22 has a radius of 15 cm from the central portion of the reforming container 11 in the reforming container 18. Are arranged to draw a circle.
  • the tip of the gas introduction pipe 23 installed in the peripheral wall 12b of the reforming container is again surrounded from the central portion inside the reforming container 11.
  • the combustion reaction by water is caused in the reforming container 18, the size of the combustion core 24 is enlarged, and the combustion reaction is continuously performed. It is possible. Also, for convenience, it is possible to periodically measure the temperature of the organic waste 15 in combustion using a thermometer instead of the temperature sensor 22.
  • FIG. 5 is an explanatory view showing the gas introduction pipe 23 in detail.
  • the gas introduction pipe 23 is a metal pipe having a diameter of about 3 cm and a total length of about 60 cm, and is installed in the reforming container peripheral wall 12b. Since the outside air is always introduced from the gas introduction pipe 23, the combustion reaction by oxygen occurs at a constant rate in the reforming container 18.
  • the gas introduction pipe 23 is located at a height of 20 cm from the discharge port 19 and introduces external air from the outside of the reforming container 11 into the reforming container 18 through holes bored in the center portions of the side surfaces.
  • three types of air ports of 15 mm, 8 mm and 5 mm in diameter can be selected as the gas inlet 23a, and it is possible to use properly depending on the type of organic waste, ventilation conditions and the like.
  • FIG. 6 is a cross-sectional view of the reforming container 11 for explaining the discharge port 19.
  • the discharge means for discharging the reformed residue 17 which has been subjected to the reforming is the reformed residue 17 accumulated in the inside of the reforming container 11 from the discharge ports 19 installed in the three directions of the reforming container peripheral wall portion 12b. Take out. Regarding recovery of the reforming residue 17, the reforming residue 17 is taken out from the outlet 19 about once every two days, but in the reaction steady process S3, in order to maintain the combustion kernel in the reaction steady state, the reforming residue 17 Be careful not to take out all the ingredients.
  • the exhaust gas processing means 21 for processing the gas discharged from the inside of the container 18 comprises a ventilation cylinder 21a, a gas collecting portion 21b, a tar removing portion 21c, and a suction fan 21d.
  • the vent cylinder 21a is externally provided on the reforming container peripheral wall portion 12b, and the gas generated by the reforming is forcedly sucked by the suction fan 21d to flow into the vent cylinder 21a, and the vent cylinder 21a After passing through, the useful gas is collected by the gas collection unit 21b.
  • the gas collection unit 21b collects the high concentration hydrogen gas.
  • the high concentration hydrogen gas generated by the reforming is collected by the hydrogen storage alloy in the gas collection unit 21b.
  • the tar removing unit 21c can play the role of a filter by laying wood pellets made of sawdust or the like and activated carbon over a plurality of layers, and purifies the gas finally discharged.
  • Example 1 In the present invention, reforming is performed using a reaction different from a combustion reaction using oxygen, which is a combustion reaction using water.
  • organic waste and water are not additionally supplied into the reforming container during the experiment for the purpose of clarifying that the combustion reaction with water occurs in the reforming container.
  • the gas generation state was measured in the gas phase part in the reforming vessel.
  • this experiment started the experiment in the state which reached the reaction steady process already.
  • Table 1 summarizes the measurement results of carbon dioxide, oxygen and nitrogen in the reforming vessel.
  • the reaction time was set to 0 minutes, 20 minutes, 41 minutes, 70 minutes and 180 minutes, and the gas generation state in the gas phase part in the reforming container was measured using a gas chromatograph and a gas chromatograph mass spectrum as a measuring device. .
  • Twenty minutes after the start of the reaction it has been shown that carbon dioxide ( 46 CO 2 ) containing 18 O is generated.
  • the isotope water H 2 18 O is used at a concentration of 10%, and 20 minutes after the start of the reaction, about 5.7% of 46 CO 2 is generated out of the total carbon dioxide. It is clear from this that about 57% of the total carbon dioxide evolved is generated by the combustion reaction of 0.5 liters of water added. Further, it is presumed that oxygen is used for the combustion reaction for maintaining the combustion nuclei and the reaction when the generated hydrogen is burned.
  • Example 2 Next, another experiment performed in this embodiment using another organic waste is shown below.
  • the purpose of this experimental example 2 is to clarify the influence on the gas generated in the reforming vessel due to the difference between the hydrolysis condition and the non-hydrolysis condition.
  • the organic waste and water were not additionally supplied into the reforming vessel as in Experimental Example 1, and the state of the gas phase in the reforming vessel was measured.
  • the experiment was started from the reaction initiation step.
  • FIG. 8 is a graph showing the amount of hydrogen generation in the gas phase in Experimental Example 2. It shows that a large amount of hydrogen gas is generated in the container from the water-containing cross paper by the combustion reaction with water as compared with the comparative example under the non-hydrolytic condition. In addition, also in the comparative example of non-hydrolysis conditions, it is guessed that the combustion reaction by water will occur by the water contained by cloth and the water generated by combustion which used oxygen.
  • FIG. 9 is a graph showing the amount of carbon monoxide generated in the gas phase in Experimental Example 2. It is shown that a large amount of carbon monoxide gas is generated in the container from the water-containing cross paper due to the combustion reaction with water as compared with the comparative example under the non-hydrolytic condition.
  • FIG. 10 is a graph showing the amount of carbon dioxide generated in the gas phase in Experimental Example 2.
  • carbon dioxide is generated by the combustion reaction using oxygen, and therefore, it is shown that the generation amount of carbon dioxide is larger than the generation ratio of carbon monoxide under the non-hydrolytic condition in FIG. It is done.
  • 11 and 12 are graphs showing amounts of oxygen and nitrogen in the gas phase in Experimental Example 2. It can be confirmed that both the oxygen and the nitrogen are reduced under the hydrolysis condition as compared with the non-hydrolysis condition. It is presumed that this is due to the decrease of these proportions due to the gas generated under the water addition condition.
  • Example 3 In the present experimental example 3, the water content optimum for hydrogen generation was investigated. In this experiment, the organic waste and water were not additionally supplied into the reforming vessel as in Experimental Examples 1 and 2, and the state of the gas phase in the reforming vessel was measured. In this experiment, the experiment was started from the reaction initiation step.
  • FIG. 13 is a graph showing the generation amount of hydrogen in the gas phase in Experimental Example 3. In hydrogen generation, it was shown that the condition of 20.0 liters as the amount of water was optimum for 30 kg of chaff.
  • Example 4 In this experimental example 4, the reaction time from the ignition of the organic waste to the disappearance of hydrogen was measured. This experiment, like the experimental examples 1 to 3, measures the state of the gas phase part in the reforming container without additionally supplying the organic waste and water into the reforming container. In this experiment, the experiment was started from the reaction initiation step.
  • the rice husk After using 30 kg of rice husk as organic waste and supplying it to the reforming vessel, add 20 liters of water to the rice husk before starting the reaction, then ignite the organic waste by the reaction of a small amount of carbide and water, Start the reaction.
  • the rice husk had a water content of about 10% by weight.
  • FIG. 14 is a graph showing the generation amount of hydrogen in the gas phase in Experimental Example 4.
  • the peak is reached at 630 minutes, and it is shown that hydrogen generation continues up to 900 minutes. It was shown that as high as 2.5% by volume of hydrogen was generated at the peak time.
  • this experiment shows the time required to reform 30 kg of rice husks with this apparatus, and if the organic waste and water are replenished in the reaction steady process, the reforming reaction continues as described above. It is street. In this experiment, almost all the rice husk was reformed at the final time (900 minutes), and only the reforming residue remained.
  • the present invention relates to a method of reforming organic matter without using external energy, and an organic waste reforming apparatus for realizing the reforming method.
  • the gas produced by reforming contains high concentration hydrogen, which can be recovered and used as hydrogen gas, and depending on the type of organic waste, utilizing the produced reforming residue as fertilizer Since it is possible, industrial applicability is extremely high.

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Abstract

A method of an organic-waste modification accompanied by the generation of high-concentration hydrogen gas and a device for modifying organic waste, the device rendering the modification method possible. The method of an organic-waste modification is characterized by comprising a reaction initiation step in which organic waste is fed to a modification vessel and a modification is initiated with a reaction initiator in some of the organic waste, a reaction expansion step in which the reaction is expanded by passing air through the modification vessel by means of a gas introduction pipe and by supplying water for conducting a combustion reaction therewith, and a steady-reaction step in which the size of a combustion core is maintained to thereby steadily perform the modification. The method is further characterized by being accompanied by the generation of high-concentration hydrogen gas.

Description

高濃度水素ガスの発生を伴う有機性廃棄物の改質方法および有機性廃棄物改質用装置Method and apparatus for reforming organic waste with generation of high concentration hydrogen gas

 本発明は、高濃度水素ガスの発生を伴う有機性廃棄物の改質方法、およびその改質方法を実現するための、有機性廃棄物改質用装置を提供する。 The present invention provides a method of reforming organic waste accompanied by generation of high concentration hydrogen gas, and an apparatus for reforming organic waste for realizing the method of reforming the waste.

 従来より、草木、穀物、生ゴミ、農作物あるいは廃棄材等のバイオマス系廃棄物およびプラスチックなどの化成品廃棄物の一般的な廃棄処理方法として、可燃物を焼却施設にて焼却する処理方法が普及している。しかしながら、この処理方法は、大量の二酸化炭素と有害物質とを含む煤煙を放出し大気汚染と地球温暖化の原因となっており、また、焼却処分のために多量の燃料を必要としエネルギー消費等の環境問題を引き起こしている。一方、これら有機性廃棄物は大量のエネルギーを内蔵しており、それを有効利用することで地球環境保全に多大の貢献をなすことは自明である。 Conventionally, as a general disposal method for biomass waste such as plants, grains, raw garbage, agricultural crops, waste materials, etc. and chemical waste such as plastics, a treatment method for incinerating combustibles in incineration facilities has spread doing. However, this treatment method emits soot containing a large amount of carbon dioxide and harmful substances, which causes air pollution and global warming, and also requires a large amount of fuel for incineration and energy consumption etc. Causing environmental problems. On the other hand, it is self-evident that these organic wastes contain a large amount of energy, and by making effective use of them, they make a great contribution to global environmental protection.

 近年、バイオマスの高効率エネルギー転換に関する研究が注目されており、クリーンなエネルギーとして水素ガスを回収するために、水蒸気改質が利用されている。水蒸気改質とは、炭化水素を1000℃前後の高温水蒸気と嫌気的に反応させ、水素ガス、メタン、一酸化炭素その他の低分子ガスに変換する方法である。その代表的なものとしてメタンの水蒸気改質があり、燃料電池やハーバーボッシュ法によるアンモニア生産などで需要の大きい水素ガスを大量に生産する唯一の方法として、工業的に極めて重要となっている(下式)。
(1):CH+HO→CO+3H
(2):CO+HO→CO+H
(1)+(2):CH+2HO→CO+4H
一方、この方法の問題点として原料としてメタンを用いることや超高温水蒸気発生のための化石燃料の大量消費、および白金など高価な触媒の必要性、等が挙げられる。これらの問題を解決するものとして様々な有機性廃棄物改質方法が提案されている。
In recent years, research on high-efficiency energy conversion of biomass has attracted attention, and steam reforming is used to recover hydrogen gas as clean energy. Steam reforming is a method of anaerobically reacting hydrocarbons with high temperature steam at around 1000 ° C. to convert them into hydrogen gas, methane, carbon monoxide and other low molecular weight gases. A typical example is steam reforming of methane, which is extremely important industrially as the only method for mass production of hydrogen gas with high demand for fuel cell and ammonia production by the Harbor Bosch method ( Below).
(1): CH 4 + H 2 O → CO + 3H 2
(2): CO + H 2 O → CO 2 + H 2
(1) + (2): CH 4 + 2H 2 O → CO 2 + 4H 2
On the other hand, problems with this method include the use of methane as a raw material, the large consumption of fossil fuel for generating ultra-high temperature steam, and the need for an expensive catalyst such as platinum. Various organic waste reforming methods have been proposed to solve these problems.

 例えば、特許文献1は、都市ごみや産業廃棄物などの廃棄物をガス化し、得られる生成ガスを燃料用ガスなどとして回収する廃棄物のガス化改質方法を開示する。 For example, Patent Document 1 discloses a gasification and reforming method of waste that gasifies waste such as municipal waste and industrial waste and recovers the resulting gas as a gas for fuel and the like.

 また、特許文献2には、産業廃棄物および一般廃棄物を有効利用することにより新たなエネルギーを得るための、廃棄物の処理方法と熱分解ガスの回収方法及び装置が提案されている。 Further, Patent Document 2 proposes a method for treating waste and a method and apparatus for recovering pyrolysis gas, in order to obtain new energy by effectively using industrial waste and general waste.

 また、特許文献3は400℃以下の比較的低温条件でもガソリンや軽油などの炭化水素系燃料を素早く且つ十分に改質でき、一酸化炭素やメタンの副生が少なく、窒素希釈を受けずコンパクトな燃料電池用燃料改質システム及び水素リッチガス製造方法を開示する。 Further, Patent Document 3 is capable of quickly and sufficiently reforming hydrocarbon fuels such as gasoline and light oil even at relatively low temperature conditions of 400 ° C. or less, and has a small amount of carbon monoxide and methane by-products, and is compact without receiving nitrogen dilution. Disclosed are a fuel reforming system and a hydrogen rich gas producing method.

特開2006-188574号公報JP, 2006-188574, A 特開平11-290810号公報JP-A-11-290810 特開2004-281227号公報JP 2004-281227 A

 しかしながら、特許文献1では、水素回収までには、ピットに集積された都市ごみや産業廃棄物等の廃棄物をプレス機で圧縮し、乾燥熱分解工程で加熱還流する上に、1200℃もの高温で改質を行なうなどの過程において、大量のエネルギーを消費しつつ、煩雑なプロセスを経る必要がある。 However, in Patent Document 1, wastes such as urban waste and industrial waste accumulated in pits are compressed with a press before hydrogen recovery, and heated to reflux in the drying and pyrolysis step, and as high as 1200 ° C. In the process of reforming at the same time, it is necessary to go through complicated processes while consuming a large amount of energy.

 また、特許文献2は、廃棄物をエネルギー化するために、熱分解炉で発生した熱分解ガスの一部を部分燃焼し1000℃以上の高温とする等、多量のエネルギーを必要とする。また、熱分解ガスを1000℃以上にするために改質炉の耐熱構造化が不可欠となり、装置自体のコストがかかるという問題点がある。 Further, Patent Document 2 requires a large amount of energy, such as partially burning a part of the pyrolysis gas generated in the pyrolysis furnace to a high temperature of 1000 ° C. or more, in order to convert waste into energy. In addition, in order to raise the temperature of the pyrolysis gas to 1000 ° C. or more, the heat-resistant structuring of the reforming furnace becomes indispensable, which causes a problem that the cost of the apparatus itself is increased.

 更に、特許文献3においては、燃料電池用燃料改質システムの配備が容易ではないことや、改質触媒、超臨界水又は亜臨界水等、必要な材料を備えるためのコスト、またシステム稼働時のエネルギー消費等の問題がある。 Furthermore, in Patent Document 3, it is not easy to deploy a fuel reforming system for a fuel cell, the cost for providing a necessary material such as a reforming catalyst, supercritical water or subcritical water, and system operation time Energy consumption and other problems.

 本発明は、前記の問題点を解決することを課題とし、有機性廃棄物の内蔵するエネルギーを簡便な方法で取り出し、水素ガスなどの有用性の高い形に変換する技術に関する。本発明による改質反応は外部からの給水のみで足り、1000℃もの高温水蒸気および高価な貴金属触媒は不要である。さらに、外部からのエネルギーを用いることなく、有機性廃棄物を極めて環境に優しい方法で改質することが可能である。本発明は、外部からのエネルギーを使用することなく有機性廃棄物を改質する方法、およびその改質方法を実現するための、有機性廃棄物改質用装置を提供する。また、有機性廃棄物の改質によって発生する高濃度水素ガスを回収し、利用することができる。 The present invention has an object to solve the above-mentioned problems, and relates to a technology for taking out the energy contained in organic waste by a simple method and converting it into a highly useful form such as hydrogen gas. The reforming reaction according to the present invention requires only external water supply, and high temperature steam as high as 1000 ° C. and an expensive precious metal catalyst are unnecessary. Furthermore, it is possible to modify organic waste in a very environmentally friendly manner without the use of external energy. The present invention provides a method of reforming organic waste without using external energy, and an organic waste reforming apparatus for realizing the reforming method. In addition, high concentration hydrogen gas generated by reforming organic waste can be recovered and used.

 請求項1に記載の有機性廃棄物の改質方法は、
有機性廃棄物を改質容器内に供給し、反応開始剤を用いて有機性廃棄物の一部において改質を開始する反応開始工程と、
気体導入管による改質容器内への通気と、水による燃焼反応を行うための給水により反応を拡大させる反応拡大工程と、
燃焼核の大きさを維持することにより改質を定常的に行う反応定常工程と、
を有し、高濃度水素ガスの発生を伴うことを特徴とする。
The method for reforming organic waste according to claim 1 is
A reaction initiation step of feeding organic waste into a reforming vessel and initiating reforming of a portion of the organic waste using a reaction initiator;
A reaction expansion step of expanding the reaction by aeration into the reforming container with a gas introduction pipe and water supply for performing a combustion reaction with water;
A steady-state reaction step in which reforming is performed in a steady manner by maintaining the size of combustion nuclei;
And is accompanied by the generation of high concentration hydrogen gas.

 請求項2に記載の有機性廃棄物の改質方法において、請求項1に記載の反応開始工程は、前記反応開始剤として少量のカーバイドと水とを用いて有機性廃棄物の一部を着火させる工程を有することを特徴とする。 The method for reforming organic waste according to claim 2, wherein the reaction initiation step according to claim 1 uses a small amount of carbide and water as the reaction initiator to ignite a portion of the organic waste. And a step of

 請求項3に記載の有機性廃棄物の改質方法において、請求項1または2に記載の反応拡大工程における改質容器内への通気は、気体導入管による改質容器内への外気の導入を調整することを特徴とする。 In the method for reforming organic waste according to claim 3, aeration into the reforming container in the reaction expansion step according to claim 1 or 2 is the introduction of outside air into the reforming container by the gas introducing pipe. It is characterized by adjusting.

 請求項4に記載の有機性廃棄物の改質方法において、請求項1~3に記載の反応拡大工程における給水は、給水手段により外部より水を連続的に補充することを特徴とする。 In the method for reforming organic waste according to claim 4, the water supply in the reaction expansion step according to claims 1 to 3 is characterized in that water is continuously replenished from the outside by a water supply means.

 請求項5に記載の有機性廃棄物の改質方法において、請求項1~4に記載の反応定常工程における燃焼核の大きさの維持は、温度センサーを用いた温度検知を基に、前記気体導入管による改質容器内への通気と、前記改質容器内への前記給水を調整することにより行うことを特徴とする。 In the method for reforming organic waste according to claim 5, the maintenance of the size of the combustion nuclei in the reaction steady process according to claims 1 to 4 is the gas based on temperature detection using a temperature sensor. It is characterized in that it is performed by aeration into the reforming container by the introduction pipe and adjusting the water supply into the reforming container.

 請求項6に記載の有機性廃棄物改質用装置は、
有機性廃棄物の供給手段と、
供給手段から供給された有機性廃棄物の改質を行う改質容器と、
有機性廃棄物の燃焼中における温度状態を把握するための温度センサーと、
改質容器内への通気を行うための気体導入管と、改質を行うため水を補充する給水手段と、
改質が行われた改質残渣を外部に排出する排出手段と、
前記改質容器から排出するガスを処理する排出ガス処理手段と、
を有し、高濃度水素ガスの発生を伴うことを特徴とする。
The apparatus for reforming organic waste according to claim 6 is
Means for supplying organic waste,
A reforming vessel for reforming organic waste supplied from the supply means;
A temperature sensor for grasping the temperature condition during combustion of organic waste,
A gas introduction pipe for ventilating the inside of the reforming container, a water supply means for replenishing water for reforming, and
An exhausting means for discharging the reformed reforming residue to the outside;
Exhaust gas processing means for processing the gas discharged from the reforming container;
And is accompanied by the generation of high concentration hydrogen gas.

 請求項1に記載の発明によれば、本発明の有機性廃棄物の改質方法は、反応定常工程において外部からのエネルギーを使用することなく継続的に改質を行うことができる。また、改質によって生成するガスは高濃度水素を含有しており、これを回収し水素ガスとして利用することができる。 According to the first aspect of the present invention, in the method for reforming organic waste of the present invention, reforming can be continuously performed without using external energy in the reaction steady process. Further, the gas generated by the reforming contains high concentration hydrogen, which can be recovered and used as hydrogen gas.

 請求項2に記載の発明によれば、反応開始工程は、前記反応開始剤として少量のカーバイドと水とを用いて有機性廃棄物の一部を着火させる工程を有することを特徴とするため、最小限のエネルギーで改質を開始することができる。 According to the second aspect of the invention, the reaction initiation step includes the step of igniting part of the organic waste using a small amount of carbide and water as the reaction initiator. Reforming can be initiated with minimal energy.

 請求項3に記載の発明によれば、反応拡大工程における改質容器内への通気は、気体導入管による改質容器内への外気の導入を調整することを特徴とするため、改質における連続反応を停止させることなく、極めて容易に行うことができる。 According to the third aspect of the present invention, in the reaction expansion step, aeration into the reforming container is characterized by adjusting the introduction of the outside air into the reforming container by the gas introduction pipe, so that in the reforming, It can be carried out extremely easily without stopping the continuous reaction.

 請求項4に記載の発明によれば、反応拡大工程における給水は、給水手段により外部より水を連続的に補充することを特徴とするため、燃焼剤などの外部からのエネルギーを用いることなく、改質を行うことができる。 According to the invention as set forth in claim 4, since the water supply in the reaction expansion step is characterized by continuously replenishing water from the outside by the water supply means, without using external energy such as a combustion agent, It can be reformed.

 請求項5に記載の発明によれば、反応定常工程における燃焼核の大きさの維持は、温度センサーを用いた温度検知を基に、前記気体導入管による改質容器内への通気と、前記改質容器内への前記給水の調整により行うことを特徴とするため、燃焼核の大きさの変化を的確に感知し、維持することが可能である。 According to the invention as set forth in claim 5, the maintenance of the size of the combustion nucleus in the reaction steady process is based on the temperature detection using the temperature sensor, the aeration into the reforming container by the gas introducing pipe, and Since the adjustment is performed by adjusting the water supply into the reforming container, it is possible to accurately sense and maintain the change in size of the combustion core.

 また本発明の有機性廃棄物改質用装置は、改質工程において密閉状態を保持可能であり、排出ガス処理手段を有しているため、臭気やその他の有害ガスが外部に漏れることなく、大量の有機性廃棄物を簡易な設備で改質することができるという利点がある。さらに、有機性廃棄物の種類によっては、生成した改質残渣、つまり灰を肥料として利用することが可能であるため、極めて環境に優しい有機性廃棄物改質方法および有機性廃棄物改質用装置を提供することができる。 Further, the apparatus for reforming organic waste according to the present invention can maintain a sealed state in the reforming process and has exhaust gas treatment means, so that odor and other harmful gases do not leak to the outside. There is an advantage that a large amount of organic waste can be reformed by simple equipment. Furthermore, depending on the type of organic waste, it is possible to use the generated reforming residue, ie, ash, as a fertilizer, so that it is possible to use an extremely environmentally friendly organic waste reforming method and organic waste reforming method. An apparatus can be provided.

有機性廃棄物改質工程のフローチャートである。It is a flowchart of an organic waste reforming process. 有機性廃棄物改質用装置の概略図である。It is the schematic of the apparatus for organic waste reforming. 有機性廃棄物改質用装置の外観図である。It is an external view of the apparatus for organic waste reformation. 温度センサーおよび燃焼核を説明する改質容器の断面図である。It is sectional drawing of a reforming container explaining a temperature sensor and a combustion nucleus. 気体導入管を説明する改質容器の断面図である。It is a sectional view of a reforming container explaining a gas introduction pipe. 排出口を説明する改質容器の断面図である。It is a sectional view of a reforming container explaining an outlet. 水による燃焼反応の化学反応式の説明図である。It is explanatory drawing of the chemical reaction formula of the combustion reaction by water. 実験例2において気相での水素量を示すグラフである。It is a graph which shows the amount of hydrogen in the gaseous phase in Experimental example 2. 実験例2において気相での一酸化炭素量を示すグラフである。It is a graph which shows the amount of carbon monoxide in a gaseous phase in Experimental example 2. 実験例2において気相での二酸化炭素量を示すグラフである。It is a graph which shows the amount of carbon dioxide in a gaseous phase in example 2 of an experiment. 実験例2において気相での酸素量を示すグラフである。It is a graph which shows the amount of oxygen in a gaseous phase in Experimental example 2. 実験例2において気相での窒素量を示すグラフである。It is a graph which shows the amount of nitrogen in a gaseous phase in Experimental example 2. 実験例3において気相での水素量を示すグラフである。It is a graph which shows the amount of hydrogen in the gaseous phase in Experimental example 3. 実験例4において気相での水素量を示すグラフである。It is a graph which shows the amount of hydrogen in the gaseous phase in Experimental example 4.

 本発明の有機性廃棄物の改質方法について説明する。改質工程については、3段階の工程に分けられる。すなわち、有機性廃棄物を改質容器内に供給し、反応開始剤を用いて有機性廃棄物の一部において改質を開始する反応開始工程、気体導入管による改質容器内への通気と、水による燃焼反応を行うための給水により反応を拡大させる反応拡大工程、燃焼核の大きさを維持することにより改質を定常的に行う反応定常工程である。 The method for reforming organic waste of the present invention will be described. The reforming process is divided into three stages. That is, a reaction start step of supplying organic waste into the reforming container and starting reforming in a part of the organic waste using the reaction initiator, aeration into the reforming container by the gas introduction pipe, The reaction expansion step is a reaction expansion step in which the reaction is expanded by water supply for carrying out a combustion reaction with water, and the reaction steady step in which reforming is performed in a steady manner by maintaining the size of the combustion core.

 まず、反応開始工程においては、所定量の有機性廃棄物を改質容器内に供給し、反応開始剤を用いて有機性廃棄物の一部を着火させることで反応を開始させる。反応開始剤としては、少量のカーバイドと水を用いることで、有機性廃棄物を着火させる。反応開始時には改質容器内には酸素を含む空気が充満し、カーバイドと水の反応によりアセチレンガスが発生するため、このアセチレンに着火することにより有機性廃棄物も瞬時に着火する。なお、有機性廃棄物の含水状態にもよるが、有機性廃棄物が初期段階で乾燥状態である場合は反応開始前に所定量の水を加えておく。 First, in the reaction start step, a predetermined amount of organic waste is supplied into the reforming container, and a reaction initiator is used to ignite a part of the organic waste to start the reaction. As a reaction initiator, organic waste is ignited by using a small amount of carbide and water. At the start of the reaction, the reforming container is filled with air containing oxygen, and acetylene gas is generated by the reaction of the carbide and water, so that the organic waste is also ignited instantaneously by igniting this acetylene. In addition, although it is based also on the water-containing state of organic waste, when organic waste is an initial stage in a dry state, a predetermined amount of water is added before reaction start.

 反応開始後、反応拡大工程においては、投入した有機性廃棄物における反応箇所を気体導入管による改質容器内への通気と、水による燃焼反応を行うための給水により拡大させる。気体導入管による改質容器内への通気により改質容器内には外気が絶えず導入されているため、酸素を使用した燃焼反応は継続的に起こっている。酸素を使用した燃焼反応によって、周辺の有機性廃棄物およびそこに含まれる水の温度が上昇し、有機性廃棄物と水との反応、すなわち水による燃焼反応が起こる。さらに、気体導入管による改質容器内への通気は、気体導入管先端部を改質容器中心部から周辺部へ移動させることで、通気状態を変化させることが可能であり、酸素を使用した燃焼反応は、有機性廃棄物中心部から周辺部へ拡大する。この酸素を使用した燃焼反応によって熱がさらに発生し、有機性廃棄物内の水による燃焼反応が拡大する。この一連の反応により、反応拡大工程においては、有機性廃棄物内における反応を拡大させることができる。一方、反応開始時に有機性廃棄物に水を加えておくことで、酸素による燃焼反応は有機性廃棄物全体には広がらない程度に抑制される。また、改質容器内の有機性廃棄物および酸素による燃焼反応で発生した燃焼物の存在により、有機性廃棄物における反応箇所では通気状態が少なからず妨げられているため、これによっても酸素による燃焼反応は有機性廃棄物全体には広がらない程度に抑制されている。 After the start of the reaction, in the reaction expansion step, the reaction site in the input organic waste is expanded by aeration into the reforming container by the gas introduction pipe and water supply for performing the combustion reaction with water. Since the outside air is constantly introduced into the reforming vessel by aeration into the reforming vessel by the gas introduction pipe, the combustion reaction using oxygen is continuously occurring. The combustion reaction using oxygen raises the temperature of the surrounding organic waste and the water contained therein, causing the reaction between the organic waste and water, that is, the water combustion reaction. Furthermore, the ventilation into the reforming container by the gas introduction pipe can change the ventilation state by moving the tip of the gas introduction pipe from the center of the reforming container to the periphery, and oxygen was used. The combustion reaction spreads from the organic waste center to the periphery. The combustion reaction using this oxygen further generates heat, and the combustion reaction by water in the organic waste is expanded. This series of reactions can expand the reaction in the organic waste in the reaction expansion step. On the other hand, by adding water to the organic waste at the start of the reaction, the combustion reaction by oxygen is suppressed to such an extent that it does not spread to the whole organic waste. In addition, the presence of the organic waste in the reforming vessel and the combustion products generated by the combustion reaction with oxygen prevent the aeration state from occurring to a small extent at the reaction site in the organic waste. The reaction is suppressed to the extent that it does not spread throughout the organic waste.

 ここで、有機性廃棄物内の水による燃焼反応について説明する。通常、狭義の燃焼反応とは、酸素による熱と光を伴う激しい酸化反応のことをいう。例えば、これを化学反応式で表すと、およそ図7(a)(b)のようになる。即ち、バイオマス等の有機性廃棄物を炭水化物(図7(a))又は炭化水素(図7(b))とすると、酸素との反応後、二酸化炭素および水を生成する反応となる。一方、本発明における水による燃焼反応とは、水を酸化剤として使用し、炭水化物または炭化水素から水素を発生させる反応である。これを化学反応式で表すと、およそ図7(c)(d)のようになる。即ち、上記同様にバイオマス等の有機性廃棄物を炭水化物(図7(c))又は炭化水素(図7(d))とすると、二酸化炭素および水素、または一酸化炭素および水素を生成する反応となる。この反応は水蒸気改質と類似する反応であるが、一般的な水蒸気改質において必要な、1000℃もの高温水蒸気および触媒は不要である。以後、燃焼反応とは、水による燃焼反応を表すこととする。 Here, the combustion reaction by water in the organic waste will be described. In general, the combustion reaction in a narrow sense refers to a violent oxidation reaction involving heat and light due to oxygen. For example, when this is expressed by a chemical reaction formula, it is approximately as shown in FIGS. 7 (a) and 7 (b). That is, assuming that organic wastes such as biomass are carbohydrates (FIG. 7 (a)) or hydrocarbons (FIG. 7 (b)), carbon dioxide and water are produced after reaction with oxygen. On the other hand, the combustion reaction with water in the present invention is a reaction using water as an oxidant to generate hydrogen from carbohydrates or hydrocarbons. If this is represented by a chemical reaction formula, it will become like FIG. 7 (c) (d). That is, assuming that organic wastes such as biomass are carbohydrates (FIG. 7 (c)) or hydrocarbons (FIG. 7 (d)) in the same manner as described above, reactions that produce carbon dioxide and hydrogen or carbon monoxide and hydrogen Become. This reaction is a reaction similar to steam reforming, but the high temperature steam and catalyst as high as 1000 ° C. necessary for general steam reforming are unnecessary. Hereinafter, the combustion reaction refers to the combustion reaction with water.

 燃焼反応が有機性廃棄物内に拡大すると、有機性廃棄物中心部では温度が300~400℃付近まで上昇する。改質容器に設置された複数本の温度センサー全てが温度上昇を検知した時点で気体導入管を改質容器内周辺部から中心部へ戻すことで、反応定常状態が形成される。この際の有機性廃棄物中心部の高温部を燃焼核と称し、またこの状態を反応定常工程と称する。燃焼核周辺部の温度は約150~200℃付近であり、また、改質容器内の気相では80℃付近、改質容器外部では40℃付近である。燃焼反応が進行することで、有機性廃棄物の改質が進むと、更に有機性廃棄物を改質容器内に供給する。また、有機性廃棄物には水を連続的に供給することで、水分不足による燃焼反応の停止を防止する。 As the combustion reaction expands into organic waste, the temperature rises to around 300-400 ° C. at the organic waste center. The reaction steady state is formed by returning the gas introduction pipe from the inner peripheral portion to the central portion of the reforming container when all the temperature sensors installed in the reforming container detect the temperature rise. The high temperature part of the organic waste core at this time is called a combustion core, and this state is called a reaction steady process. The temperature around the combustion core is about 150 to 200 ° C., and the gas phase in the reforming vessel is about 80 ° C., and the outside of the reforming vessel is about 40 ° C. As the combustion reaction progresses, when the reforming of the organic waste proceeds, the organic waste is further supplied into the reforming container. In addition, by continuously supplying water to the organic waste, the termination of the combustion reaction due to the lack of water is prevented.

 燃焼核が収縮した場合には、上記反応拡大工程と同様、改質容器周壁部に設置された気体導入管の気体導入管先端部を改質容器中心部から周辺部へ移動させることで、酸素による燃焼反応を拡大させ、再度反応拡大工程から改質工程を繰り返すことが可能である。この際にも特に外部からのエネルギーを用いる必要はなく、気体導入管による改質容器内への通気と、水による燃焼反応を行うための給水により反応を拡大させ、反応定常工程へと至らしめることが可能である。また、燃焼核が拡大し過ぎた場合には、気体導入管による通気量を減少させることで酸素による燃焼反応を調節することが可能である。改質容器周壁部に設置された気体導入管の気体導入管先端部を改質容器中心部から周辺部へ移動させることにより酸素による燃焼反応が拡大しない場合は、有機性廃棄物を改質容器内に供給し、改質容器内に設置された複数本の温度センサー全てが温度上昇を検知するまで数時間程度そのまま放置する。温度上昇が検知された場合は、気体導入管を改質容器内周辺部から中心部へ戻すとともに改質容器内に水を供給し、反応定常工程を継続させる。以上の様に3段階の改質工程により、外部からのエネルギー供給を行うことなく有機性廃棄物を改質することが可能となる。また、水を供給するタイミングについては、排出ガスの水素濃度を検知し、水素濃度が例えば2%を下回った時点で水を供給してもよい。 When the combustion nuclei are contracted, oxygen is moved by moving the tip end of the gas introduction pipe of the gas introduction pipe installed in the peripheral wall of the reforming container from the center of the reforming container to the periphery as in the reaction expansion step. It is possible to expand the combustion reaction by and repeat the reforming step from the reaction expansion step again. Also in this case, it is not necessary to use external energy, and the reaction can be expanded by aeration into the reforming container with a gas introduction pipe and water supply for performing a combustion reaction with water, leading to a reaction steady process. It is possible. In addition, when the combustion nuclei are expanded too much, it is possible to adjust the combustion reaction by oxygen by reducing the amount of aeration through the gas introduction pipe. When the combustion reaction due to oxygen is not expanded by moving the tip of the gas introduction pipe of the gas introduction pipe installed in the peripheral wall of the reforming container from the center of the reforming container to the peripheral part, the organic waste is used as the reforming container It is supplied to the inside and left for several hours until all the temperature sensors installed in the reforming container detect the temperature rise. When a temperature rise is detected, the gas introduction pipe is returned from the inner peripheral portion to the central portion of the reforming container and water is supplied into the reforming container to continue the reaction steady process. As described above, the three-stage reforming process makes it possible to reform organic waste without external energy supply. In addition, as to the timing of supplying water, the hydrogen concentration of the exhaust gas may be detected, and water may be supplied when the hydrogen concentration falls below 2%, for example.

 なお、本発明でいう有機性廃棄物とは、生ゴミ、廃紙材、草等のバイオマス、ゴム・プラスチック類等の天然および合成有機性廃棄物を含む有機性廃棄物を想定しているが、これらに限定されるものではない。 In the present invention, organic waste is assumed to be organic waste including natural and synthetic organic waste such as garbage, waste paper, biomass such as grass, rubber and plastics etc. Not limited to these.

 次に、本発明の有機性廃棄物の改質方法に用いられる有機性廃棄物の改質用装置について説明する。有機性廃棄物の改質用装置は、有機性廃棄物の供給手段と、供給手段から供給された有機性廃棄物の改質を行う改質容器と、有機性廃棄物の燃焼中における温度状態を把握するための温度センサーと、改質容器内への通気を行うための気体導入管と、改質を行うため水を補充する給水手段と、改質が行われた改質残渣を外部に排出する排出手段と、前記改質容器から排出するガスを処理する排出ガス処理手段とを有する。 Next, an apparatus for reforming organic waste used in the method for reforming organic waste of the present invention will be described. The apparatus for reforming organic waste comprises an organic waste supply means, a reforming container for reforming the organic waste supplied from the supply means, and a temperature state during combustion of the organic waste. Temperature sensor for grasping the gas, a gas introduction pipe for ventilating the inside of the reforming container, water supply means for replenishing water for reforming, and the reforming residue subjected to reforming to the outside It has the discharge | emission means to discharge | emit, and the exhaust gas processing means to process the gas discharged | emitted from the said reforming container.

 本発明の有機性廃棄物の改質用装置における有機性廃棄物の供給手段は、供給口と供給口蓋体からなる。供給口は、改質容器天井部に開口する形で形成され、有機性廃棄物の供給が行われる。天井部に供給口を設置することで改質容器内に均一に有機性廃棄物を供給することが可能となる。 The means for supplying organic waste in the apparatus for reforming organic waste according to the present invention comprises a supply port and a supply port cover. The supply port is formed in such a manner as to open to the reformer container ceiling, and supply of organic waste is performed. By providing the supply port at the ceiling, it is possible to uniformly supply the organic waste into the reforming container.

 改質容器は、容器壁と、脚部とからなる。 The reforming container comprises a container wall and a leg.

 容器壁は、平面正六角形状の天井部と、天井部の外周縁部から下方に周設された周壁部と、天井部と同様平面正六角形状の底部からなる。なお、周壁部は、耐火性壁部と、耐火性壁部を被覆する外壁部とから構成する構造が好ましいが、簡易的には通常用いられる鋼板によって形成される。鋼板は約10cm程度の厚みを有することが好ましい。 The container wall comprises a flat regular hexagonal ceiling, a peripheral wall provided below the outer peripheral edge of the ceiling, and a flat regular hexagonal bottom similar to the ceiling. The peripheral wall portion is preferably formed of a fire-resistant wall portion and an outer wall portion covering the fire-resistant wall portion. However, the peripheral wall portion is simply formed of a generally used steel plate. The steel plate preferably has a thickness of about 10 cm.

 脚部は、周壁部の下端部に複数本取り付けられ、約50cm程度の同一の長さからなることで改質容器を地上から一定の高さに設置できる。また、設置地点に傾斜がある場合には、脚部の長さを調節することで、改質容器を水平に保持することができる。 A plurality of leg portions are attached to the lower end portion of the peripheral wall portion, and the reforming container can be installed at a certain height from the ground by being formed with the same length of about 50 cm. In addition, when the installation point is inclined, the reforming container can be held horizontally by adjusting the length of the legs.

 改質容器は、約1000リットルの容量を有する、底部および天井部の1辺が約60cmの正六角形、底部から天井部までの高さ約1mの正六角柱形状の容器であるが、容量、サイズはこれに限定されるものではない。また、形状も正六角柱形状に限定されるものではなく、円筒形状等でもよい。 The reforming container is a container having a volume of about 1000 liters, a regular hexagonal shape of about 60 cm on one side of the bottom and the ceiling, and a regular hexagonal column shape having a height of about 1 m from the bottom to the ceiling. Is not limited to this. Further, the shape is not limited to a regular hexagonal column shape, and may be a cylindrical shape or the like.

 有機性廃棄物の燃焼中における温度状態を把握するための温度センサーは、改質容器内に複数本設置されており、温度検知部位が改質容器の外壁部から改質容器内部に突出され、改質容器内の燃焼中の有機性廃棄物の温度を検知する。温度センサーは、燃焼中の有機性廃棄物中の燃焼核の大きさを測定する役割を果たす。具体的には、温度センサーは、直径約1~5cm、全長約50cmの円筒形状のもので、温度検知部位、本体、表示部からなり、正六角柱の各側面中央部に穿設された孔から改質容器内に突出しており、温度検知部位が燃焼中の有機性廃棄物の温度を検知できる。穿設孔は、改質容器底部から約50cmの高さに位置しており、改質容器が正六角柱形状を有する場合には、改質容器の6側面部から各々1本ずつ、計6本の温度センサーが改質容器内の温度検知に使用され、各々の温度センサーの温度検知部位は改質容器内で容器中心部から半径15cm程度の大きさの円を描くように配置される。反応定常工程においては、温度センサーのうち少なくとも1本が3分間以上200℃を下回る温度を計測した時点で、気体導入管の気体導入管先端部を改質容器中心部から周辺部へ移動させることで、有機性廃棄物内の燃焼核の大きさを拡大させ、加えて給水手段より改質容器内に給水を行うことで、燃焼反応を継続的に行うことが可能である。温度検知部位が検知する温度は表示部で確認することができる。 A plurality of temperature sensors for grasping the temperature state during combustion of the organic waste are installed in the reforming container, and the temperature detection portion is projected from the outer wall portion of the reforming container into the inside of the reforming container, The temperature of the organic waste during combustion in the reforming vessel is detected. The temperature sensor serves to measure the size of combustion nuclei in the organic waste being burned. Specifically, the temperature sensor has a cylindrical shape with a diameter of about 1 to 5 cm and a total length of about 50 cm, and comprises a temperature detection portion, a main body, and a display portion. Protruding into the reforming vessel, the temperature detection site can detect the temperature of the organic waste being burned. The drilling holes are located at a height of about 50 cm from the bottom of the reforming container, and when the reforming container has a regular hexagonal column shape, a total of six holes, one each from the six side portions of the reforming container The temperature sensor in the reforming vessel is used to sense the temperature in the reforming vessel, and the temperature sensing portion of each temperature sensor is arranged in a circle with a radius of about 15 cm from the center of the vessel in the reforming vessel. In the reaction steady process, when the temperature of at least one of the temperature sensors is less than 200 ° C. for 3 minutes or more, the tip end of the gas introduction pipe of the gas introduction pipe is moved from the center of the reforming container to the periphery Then, the combustion reaction can be continuously performed by expanding the size of the combustion nucleus in the organic waste and supplying water from the water supply means into the reforming container. The temperature detected by the temperature detection part can be confirmed by the display unit.

 改質容器内への通気を行うための気体導入管は、直径約3cm、全長約60cm程度の金属製管であり、改質容器周壁部に設置される。常時気体導入管先端部から外気が導入されているため、改質容器内では酸素による燃焼反応が一定の割合で絶えず起こっている。気体導入管は、改質容器の下端部から高さ約20cmに位置し、改質容器周壁部の各側面中央部に穿設された孔を通して、改質容器外部より改質容器内へ外気を導入する。気体導入管は移動させることが可能であり、位置を固定されることなく、改質容器内において通気位置を調節することが可能である。また、改質容器内への通気量を増やすため、気体導入管の管側面に小孔を穿設することもできる。 The gas introducing pipe for ventilating the inside of the reforming container is a metal pipe having a diameter of about 3 cm and a total length of about 60 cm, and is installed on a peripheral wall of the reforming container. Since outside air is always introduced from the tip of the gas introduction pipe, the combustion reaction by oxygen is constantly occurring at a constant rate in the reforming container. The gas introduction pipe is located at a height of about 20 cm from the lower end of the reforming container, and through the holes bored in the center of each side of the peripheral wall of the reforming container, the outside air is introduced into the reforming container from the outside of the reforming container. Introduce. The gas introduction pipe can be moved, and the vent position can be adjusted in the reforming container without being fixed in position. Further, in order to increase the amount of air flow into the reforming container, it is possible to form a small hole on the side of the gas introduction pipe.

 改質を行うため水を補充する給水手段は、給水タンクと改質容器内で燃焼中の有機性廃棄物に給水を行うシャワー部からなる。給水タンクは、前記改質容器天井部の中央部に設けられており、給水タンク内に常時貯水しておくことができる。給水タンクとシャワー部とは給水タンク下部蓋体で仕切られており、必要に応じて水を給水タンク内からシャワー部に送ることができる。シャワー部のシャワーヘッドには多数の孔が開いており、水が噴霧されることで、改質容器内部の燃焼中の有機性廃棄物全体に満遍なく水が行き渡るような構造となっている。シャワーヘッドは球体形状をしているが、これに限定されるものではない。1回の給水量は、有機性廃棄物の含水量と給水量の合計量が、有機性廃棄物の重量を超えないよう調整することが好ましい。また、簡便的に給水を行うにあたっては、有機性廃棄物の供給口を開口して給水することも可能である。 A water supply means for replenishing water for reforming includes a water supply tank and a shower portion for supplying water to the organic waste being burned in the reforming container. The water supply tank is provided at the center of the ceiling of the reforming container, and can be constantly stored in the water supply tank. The water supply tank and the shower unit are separated by a lower cover of the water supply tank, and water can be sent from the inside of the water supply tank to the shower unit as needed. A large number of holes are opened in the shower head of the shower section, and the structure is such that water is evenly distributed to the entire organic waste during combustion inside the reforming container by spraying water. The showerhead has a spherical shape, but is not limited thereto. It is preferable to adjust the water supply amount at one time so that the total amount of the water content of the organic waste and the water supply amount does not exceed the weight of the organic waste. Moreover, in order to supply water simply, it is also possible to open the supply port of organic waste and to supply water.

 改質が行われた改質残渣を外部に排出する排出手段は、改質容器周壁部に設置された排出口から、内部に蓄積した改質残渣を取り出す。有機性廃棄物は改質され、生成した改質残渣は排出口付近に集積する。排出口は改質容器周壁部に複数設置することが可能である。改質残渣の回収については、有機性廃棄物から改質残渣の生成において減容率が大きいため、およそ2日に1回の割合で改質残渣を取り出す。取り出した改質残渣は、有機性廃棄物の種類によっては、肥料として利用することが可能である。また、排出口の位置はこれに限定されるものではなく、排出口を改質容器底部に設置することも可能である。なお、排出口付近には改質容器内の過剰な水を取り出すための排水口を設けることが好ましい。 The discharging means for discharging the reformed reforming residue to the outside takes out the reforming residue accumulated inside from the exhaust port installed in the reforming container peripheral wall portion. The organic waste is reformed, and the generated reforming residue accumulates near the outlet. A plurality of discharge ports can be installed in the reforming container peripheral wall portion. With regard to recovery of the reforming residue, the reforming residue is removed at a rate of about once every two days because the volume reduction rate is large in the formation of the reforming residue from the organic waste. The reformed residue taken out can be used as fertilizer depending on the type of organic waste. Further, the position of the discharge port is not limited to this, and the discharge port can also be installed at the bottom of the reforming container. In addition, it is preferable to provide a drainage port for taking out excess water in the reforming container in the vicinity of the discharge port.

 改質容器から排出するガスを処理する排出ガス処理手段は、通気筒体、ガス捕集部、タール除去部、吸引ファンからなる。通気筒体は改質容器周壁部に外設されており、改質により発生したガスが吸引ファンによって強制的に吸引されることで通気筒体内に流入し、通気筒体を通過した後、ガス捕集部で有用なガスが捕集される。本発明に係る有機性廃棄物改質用装置では、改質工程において有用な水素ガスが高濃度で発生するため、ガス捕集部において水素ガスを捕集するが、本発明はこれに限定するものではなく、ガス捕集部では適宜必要なガスに応じて捕集手段を変更することが可能である。また、ガス捕集部は、改質容器天井部に貫通孔を穿設することで設置し、改質容器内から直接水素を捕集することも可能である。タール除去部では、おが屑等からなる木質ペレット等や、活性炭を敷設することで、フィルターの役割を担うことができ、最終的に排出するガスを浄化することが可能である。 The exhaust gas processing means for processing the gas discharged from the reforming container comprises a vent cylinder, a gas collecting portion, a tar removing portion and a suction fan. The aeration cylinder is provided outside the peripheral wall of the reforming container, and the gas generated by the modification is forced to be sucked by the suction fan to flow into the aeration cylinder and pass through the aeration cylinder. Useful gas is collected in the collection section. In the apparatus for reforming organic waste according to the present invention, hydrogen gas useful in the reforming step is generated at a high concentration, so the hydrogen gas is collected in the gas collection unit, but the present invention is limited thereto It is possible to change the collection means according to the necessary gas appropriately in the gas collection unit. In addition, the gas collection portion can be installed by forming a through hole in the top of the reforming container, and hydrogen can be collected directly from the inside of the reforming container. In the tar removing unit, by laying wood pellets made of sawdust or the like or activated carbon, it can play the role of a filter, and it is possible to purify the gas finally discharged.

 改質によって発生する高濃度水素ガスは、例えばガス捕集部において水素吸蔵合金により捕集されるが、水素の回収方法はこれに限られるものではなく、公知の水素回収手段を用いることができる。また、同時に水素濃度を検出する水素センサー又はガス分析装置を備えてもよい。 The high concentration hydrogen gas generated by the reforming is collected by, for example, a hydrogen storage alloy in the gas collection unit, but the hydrogen recovery method is not limited thereto, and a known hydrogen recovery means can be used. . In addition, a hydrogen sensor or a gas analyzer that simultaneously detects the hydrogen concentration may be provided.

 また、改質容器内には圧力計を設置し、改質工程における改質容器内の圧力を計測することで、容器内の減圧状態を保持できるよう吸引ファンによる吸引を調整することが好ましい。 In addition, it is preferable to set a pressure gauge in the reforming container and measure the pressure in the reforming container in the reforming step to adjust the suction by the suction fan so that the reduced pressure state in the container can be maintained.

 さらに、改質容器内には酸素濃度計を設置し、改質工程における改質容器内の酸素濃度を測定することで、容器内の酸素状態を保持することが好ましい。 Furthermore, it is preferable to maintain the oxygen state in the container by installing an oximeter in the reforming container and measuring the oxygen concentration in the reforming container in the reforming step.

 上記の通り、有機性廃棄物の供給、水の補充、改質容器内への通気および改質残渣の排出を連続的に行うことによって、外部からのエネルギーを用いることなく、半永久的に有機性廃棄物改質用装置の運転を継続することが可能となる。以下、本発明の実施形態について図面を用いて詳細に説明する。 As described above, by continuously supplying organic waste, replenishing water, venting into the reforming container, and discharging the reforming residue, semipermanently organic without using external energy It is possible to continue the operation of the waste reforming apparatus. Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings.

 図1は、本発明の有機性廃棄物改質工程のフローチャートである。改質工程については、3段階の工程に分けられる。すなわち、有機性廃棄物を改質容器内に供給し、反応開始剤を用いて有機性廃棄物の一部において改質を開始する反応開始工程S1、気体導入管による改質容器内の改質容器内への通気と、水による燃焼反応を行うための給水により反応を拡大させる反応拡大工程S2、燃焼核の大きさを維持することにより改質を定常的に行う反応定常工程S3である。有機性廃棄物の種類、含水量等の条件によるが、反応拡大工程S2は約600分程度継続し、その後反応定常工程S3へと至る。反応定常工程S3へ至った後、燃焼核が安定的に存在しない場合は、再度反応拡大工程S2を繰り返し、燃焼核を形成させる。また、図示するように、反応定常工程S3において、温度センサーにより200℃以下の温度低下が認められた場合は、気体導入管を改質容器内周辺部へ移動することにより、酸素を使用した燃焼反応を拡大させ、温度センサー全てが200℃を検知した時点で気体導入管を改質容器内中央部へ戻すことで、反応定常工程S3を維持する。気体導入管を改質容器内周辺部へ移動させても温度上昇が認められない場合は、有機性廃棄物を供給し、温度上昇が認められた場合は、上記と同様に気体導入管を改質容器内中央部へ戻すことで、反応定常工程S3を維持する。有機性廃棄物を供給しても温度上昇が認められない場合は、さらに有機性廃棄物を供給する。なお、気体導入管を改質容器内中央部に戻す際に、水を供給し、燃焼反応を継続させるが、水を供給するタイミングについては、排出ガスの水素濃度を検知し、水素濃度が例えば2%を下回った時点で水を供給してもよい。 FIG. 1 is a flow chart of the organic waste reforming process of the present invention. The reforming process is divided into three stages. That is, a reaction start step S1 of supplying organic waste into the reforming container and starting reforming in a part of the organic waste using the reaction initiator, reforming in the reforming container by the gas introduction pipe The reaction expansion step S2 is a reaction expansion step S2 in which the reaction is expanded by aeration in the container and water supply for performing a combustion reaction with water, and a reaction steady step S3 in which reforming is performed in a steady manner by maintaining the size of the combustion core. Depending on conditions such as the type of organic waste and the water content, the reaction expansion step S2 is continued for about 600 minutes, and then the reaction steady step S3 is performed. After reaching the reaction steady process S3, if the combustion nucleus does not stably exist, the reaction expansion process S2 is repeated again to form the combustion nucleus. Further, as shown in the figure, when a temperature decrease of 200 ° C. or less is recognized by the temperature sensor in the reaction steady process S3, the combustion using oxygen is performed by moving the gas introduction pipe to the inner peripheral portion of the reforming container. The reaction steady process S3 is maintained by expanding the reaction and returning the gas introduction pipe to the central portion inside the reforming container when all the temperature sensors detect 200.degree. If temperature rise is not recognized even if the gas introduction pipe is moved to the inner peripheral part of the reforming container, organic waste is supplied, and if temperature rise is observed, the gas introduction pipe is modified in the same manner as above. By returning to the central part in the quality container, the reaction steady process S3 is maintained. If the temperature rise is not recognized even if the organic waste is supplied, the organic waste is further supplied. In addition, when the gas introduction pipe is returned to the central portion inside the reforming container, water is supplied to continue the combustion reaction, but for the timing of supplying water, the hydrogen concentration of the exhaust gas is detected, and the hydrogen concentration is Water may be supplied when it falls below 2%.

 図2、図3はそれぞれ有機性廃棄物改質用装置10の概略図、外観図である。図において、有機性廃棄物改質用装置10は、供給手段13から供給された有機性廃棄物15の改質を行う改質容器11と、有機性廃棄物15の燃焼中における温度状態を把握するための温度センサー22と、改質容器内18への通気を行うための気体導入管23と、改質を行うため水を補充する給水手段20と、改質が行われた改質残渣17を外部に排出する排出口19と、前記改質容器11から排出するガスを処理する排出ガス処理手段21とを有する。 2 and 3 are a schematic view and an external view of the organic waste reforming apparatus 10, respectively. In the figure, the organic waste reforming apparatus 10 grasps the temperature condition of the organic waste 15 during combustion and the reforming container 11 for reforming the organic waste 15 supplied from the supply means 13. Temperature sensor 22, a gas introduction pipe 23 for ventilating the inside of the reforming container 18, water supply means 20 for replenishing water for reforming, and a reforming residue 17 for which reforming is performed And an exhaust gas processing means 21 for processing the gas discharged from the reforming container 11.

 供給手段13は、有機性廃棄物を受け入れて改質容器11の容器内18へ供給する供給口13aと、供給口13aに嵌合する供給口蓋体13bから構成される。 The supply means 13 includes a supply port 13a for receiving the organic waste and supplying the organic waste to the inside 18 of the reforming container 11, and a supply port cover 13b fitted to the supply port 13a.

 有機性廃棄物の改質を行う改質容器11は、天井部12a、周壁部12b、底部12cからなる容器壁12、脚部16から構成される。改質容器11は正六角柱形状の容器であり、1辺が約60cmの正六角形、全体の高さが約1mの、1000リットルの容量を有する容器である。 The reforming container 11 for reforming organic waste is composed of a container wall 12 including a ceiling 12a, a peripheral wall 12b, and a bottom 12c, and a leg 16. The reforming container 11 is a container having a regular hexagonal column shape, and is a container having a volume of 1000 liters and having a regular hexagon of about 60 cm on one side and a total height of about 1 m.

 脚部16は、底部12cに6本設置され、約50cm程度の同一の長さからなることで、改質容器11を地上から一定の高さに設置できる。また、設置地点に傾斜がある場合には、脚部16の長さを調節することで、改質容器11を水平に保持することができる。 The six leg portions 16 are installed at the bottom portion 12c and have the same length of about 50 cm, so that the reforming container 11 can be installed at a certain height from the ground. Further, when the installation point is inclined, the reforming container 11 can be held horizontally by adjusting the length of the leg portion 16.

 本実施例においては、約30kgの有機性廃棄物15として籾殻を用い、有機性廃棄物15が供給手段13から改質容器11に供給された後、少量のカーバイドと水を用いて反応させることで、有機性廃棄物15を着火させる。この際、有機性廃棄物15が乾燥状態である場合は、約20リットルの水を着火前に有機性廃棄物15に加え、よく撹拌しておく。反応開始後は、気体導入管23による改質容器内18への通気と、水による燃焼反応を行うための給水により反応箇所を拡大させる。この際には、気体導入管23先端部を改質容器11中心部から周辺部へ移動させることで、酸素を使用した燃焼反応を有機性廃棄物15中心部から周辺部へと拡大させる。酸素を使用した燃焼反応によって有機性廃棄物15中には熱が蓄積しており、供給された水は潜熱によって有機性廃棄物15中の温度を上昇させ、有機性廃棄物15内で水による燃焼反応が起こる。反応拡大工程S2では、有機性廃棄物15中心部の温度上昇を伴うが、中心部の温度が400℃に到達した際に、5リットルの給水を1回行い、反応箇所を拡大させる。 In the present embodiment, rice husk is used as about 30 kg of organic waste 15, and after the organic waste 15 is supplied from the supply means 13 to the reforming container 11, a reaction is performed using a small amount of carbide and water. The organic waste 15 is ignited. At this time, when the organic waste 15 is in a dry state, about 20 liters of water is added to the organic waste 15 before ignition and stirred well. After the start of the reaction, the reaction site is expanded by aeration into the reforming container 18 by the gas introduction pipe 23 and water supply for performing a combustion reaction with water. At this time, the tip end of the gas introduction pipe 23 is moved from the central portion of the reforming container 11 to the peripheral portion to expand the combustion reaction using oxygen from the central portion of the organic waste 15 to the peripheral portion. Heat is accumulated in the organic waste 15 by the combustion reaction using oxygen, and the supplied water raises the temperature in the organic waste 15 by the latent heat, and the water in the organic waste 15 A combustion reaction occurs. In the reaction expansion step S2, although the temperature rise of the central portion of the organic waste 15 is accompanied, when the temperature of the central portion reaches 400 ° C., 5 liters of water supply is performed once to enlarge the reaction site.

 燃焼反応が有機性廃棄物15内に拡大すると、有機性廃棄物15中心部では温度が400℃付近まで上昇し、定常状態が形成される。この際には、気体導入管23先端部を改質容器11内周辺部から中心部に戻すことで、反応定常状態が形成される。図4に示すように、この際には有機性廃棄物15中心部の高温部に燃焼核24が形成される。燃焼核24は有機性廃棄物15中心部に約直径30cm程度の球体状に形成され、反応定常工程S3ではほぼ一定の大きさを保持する。燃焼核周辺部25の温度は約180℃付近であり、また、改質容器内18では80℃付近、改質容器11外部では40℃付近である。燃焼反応が進行することにより、有機性廃棄物15の改質が進んだ段階で、有機性廃棄物を改質容器内18に追加的に5kg程度供給する。また、有機性廃棄物15には給水手段20により水を連続的に供給することで、水分不足による燃焼反応の停止を防止する。この際には1回の給水量が、投入した有機性廃棄物の乾燥重量を超えないように給水量を調整する。 When the combustion reaction expands into the organic waste 15, the temperature rises to around 400 ° C. in the center of the organic waste 15, and a steady state is formed. At this time, the reaction steady state is formed by returning the tip portion of the gas introduction pipe 23 from the inner peripheral portion of the reforming container 11 to the central portion. As shown in FIG. 4, at this time, a combustion nucleus 24 is formed in the high temperature portion of the central portion of the organic waste 15. The combustion nucleus 24 is formed in the center of the organic waste 15 in the form of a sphere having a diameter of about 30 cm, and maintains a substantially constant size in the reaction steady process S3. The temperature of the combustion core peripheral portion 25 is around 180 ° C., around 80 ° C. in the reforming vessel 18 and around 40 ° C. outside the reforming vessel 11. By the progress of the combustion reaction, when the reforming of the organic waste 15 progresses, the organic waste is additionally supplied to the inside of the reforming container 18 by about 5 kg. Further, by continuously supplying water to the organic waste 15 by the water supply means 20, the stop of the combustion reaction due to the lack of water is prevented. At this time, the amount of water supplied is adjusted so that the amount of water supplied once does not exceed the dry weight of the input organic waste.

 温度センサー22は、図4の通り、直径5cm、全長約50cmの円筒形状のもので、温度検知部位22a、本体22b、表示部22cからなり、改質容器周壁部12bの各側面中央部に穿設された穿設孔14から改質容器内18に突出しており、温度検知部位22aが燃焼中の有機性廃棄物15の温度を検知する。温度検知部位22aは温度センサー22の先端から約5cmの範囲であれば温度を検知することが可能である。穿設孔14は、改質容器底部12cから約50cmの高さに位置しており、各々の温度センサー22の温度検知部位22aは、改質容器内18で改質容器11中心部から半径15cmの円を描くように配置されている。温度センサー22のうち少なくとも1本が3分間以上200℃を下回る温度を計測した時点で、改質容器周壁部12bに設置された気体導入管23先端部を再度改質容器11内中心部から周辺部へ移動させ、酸素による燃焼反応を拡大させてから給水を行うことで、水による燃焼反応を改質容器内18で起こし、燃焼核24の大きさを拡大させ、燃焼反応を継続的に行うことが可能である。また、簡便的には、温度センサー22の代わりに温度計を用いて定期的に燃焼中の有機性廃棄物15の温度を計測することもできる。 As shown in FIG. 4, the temperature sensor 22 has a cylindrical shape with a diameter of 5 cm and a total length of about 50 cm, and comprises a temperature detection portion 22a, a main body 22b, and a display portion 22c. A temperature detection portion 22 a protrudes from the provided drilling hole 14 into the reforming container 18, and detects the temperature of the organic waste 15 during combustion. The temperature detection portion 22 a can detect the temperature within a range of about 5 cm from the tip of the temperature sensor 22. The drilled hole 14 is located at a height of about 50 cm from the bottom of the reforming container 12c, and the temperature detection portion 22a of each temperature sensor 22 has a radius of 15 cm from the central portion of the reforming container 11 in the reforming container 18. Are arranged to draw a circle. When at least one of the temperature sensors 22 measures a temperature below 200 ° C. for 3 minutes or more, the tip of the gas introduction pipe 23 installed in the peripheral wall 12b of the reforming container is again surrounded from the central portion inside the reforming container 11. By moving to a part and expanding the combustion reaction by oxygen and then supplying water, the combustion reaction by water is caused in the reforming container 18, the size of the combustion core 24 is enlarged, and the combustion reaction is continuously performed. It is possible. Also, for convenience, it is possible to periodically measure the temperature of the organic waste 15 in combustion using a thermometer instead of the temperature sensor 22.

 図5は気体導入管23の詳細を示す説明図である。気体導入管23は、直径約3cm、全長約60cm程度の金属製管であり、改質容器周壁部12bに設置される。常時気体導入管23から外気が導入されているため、改質容器内18では酸素による燃焼反応が一定の割合で起こっている。気体導入管23は、排出口19から高さ20cmに位置し、各側面中央部に穿設された孔を通して改質容器11外部より改質容器内18へ外気を導入する。なお、気体導入口23aは図5の通り、直径15mm、8mm、5mmの3種類の空気口を選択することができ、有機性廃棄物の種類、通気条件等により使い分けることが可能である。 FIG. 5 is an explanatory view showing the gas introduction pipe 23 in detail. The gas introduction pipe 23 is a metal pipe having a diameter of about 3 cm and a total length of about 60 cm, and is installed in the reforming container peripheral wall 12b. Since the outside air is always introduced from the gas introduction pipe 23, the combustion reaction by oxygen occurs at a constant rate in the reforming container 18. The gas introduction pipe 23 is located at a height of 20 cm from the discharge port 19 and introduces external air from the outside of the reforming container 11 into the reforming container 18 through holes bored in the center portions of the side surfaces. As shown in FIG. 5, three types of air ports of 15 mm, 8 mm and 5 mm in diameter can be selected as the gas inlet 23a, and it is possible to use properly depending on the type of organic waste, ventilation conditions and the like.

 図6は排出口19を説明する改質容器11の断面図である。改質が行われた改質残渣17を外部に排出する排出手段は、改質容器周壁部12bの3方向に設置された排出口19から改質容器11の内部に蓄積した改質残渣17を取り出す。改質残渣17の回収については、2日に1回程度、改質残渣17を排出口19から取り出すが、反応定常工程S3においては、反応定常状態の燃焼核を維持するために改質残渣17を全て取出さないように注意する。 FIG. 6 is a cross-sectional view of the reforming container 11 for explaining the discharge port 19. The discharge means for discharging the reformed residue 17 which has been subjected to the reforming is the reformed residue 17 accumulated in the inside of the reforming container 11 from the discharge ports 19 installed in the three directions of the reforming container peripheral wall portion 12b. Take out. Regarding recovery of the reforming residue 17, the reforming residue 17 is taken out from the outlet 19 about once every two days, but in the reaction steady process S3, in order to maintain the combustion kernel in the reaction steady state, the reforming residue 17 Be careful not to take out all the ingredients.

 容器内18から排出するガスを処理する排出ガス処理手段21は、通気筒体21a、ガス捕集部21b、タール除去部21c、吸引ファン21dからなる。通気筒体21aは改質容器周壁部12bに外設されており、改質により発生したガスが吸引ファン21dによって強制的に吸引されることで通気筒体21a内に流入し、通気筒体21aを通過した後、ガス捕集部21bで有用なガスが捕集される。本実施例では、改質工程において有用な水素ガスが高濃度で発生するため、ガス捕集部21bにおいて高濃度水素ガスを捕集する。改質によって発生する高濃度水素ガスは、ガス捕集部21bにおいて水素吸蔵合金により捕集される。タール除去部21cは、おが屑等からなる木質ペレットや、活性炭を複数層にわたり敷設することで、フィルターの役割を担うことができ、最終的に排出するガスを浄化する。 The exhaust gas processing means 21 for processing the gas discharged from the inside of the container 18 comprises a ventilation cylinder 21a, a gas collecting portion 21b, a tar removing portion 21c, and a suction fan 21d. The vent cylinder 21a is externally provided on the reforming container peripheral wall portion 12b, and the gas generated by the reforming is forcedly sucked by the suction fan 21d to flow into the vent cylinder 21a, and the vent cylinder 21a After passing through, the useful gas is collected by the gas collection unit 21b. In the present embodiment, since hydrogen gas useful in the reforming process is generated at a high concentration, the gas collection unit 21b collects the high concentration hydrogen gas. The high concentration hydrogen gas generated by the reforming is collected by the hydrogen storage alloy in the gas collection unit 21b. The tar removing unit 21c can play the role of a filter by laying wood pellets made of sawdust or the like and activated carbon over a plurality of layers, and purifies the gas finally discharged.

 以上、本発明に係る実施の形態であるが、本発明の技術的範囲は上記実施の形態に記載の範囲には限定されず、上記実施の形態に、多種多様な技術的変更を加えることによる実施の形態もまた、本発明の技術的範囲に属することは当業者に明らかである。 As mentioned above, although it is an embodiment concerning the present invention, the technical scope of the present invention is not limited to the range given in the above-mentioned embodiment, By adding various technical changes to the above-mentioned embodiment It will be apparent to those skilled in the art that the embodiments are also within the technical scope of the present invention.

 次に、本実施形態による有機性廃棄物改質用装置の運転例を以下の実験例1~4に示す。 Next, an operation example of the apparatus for reforming organic waste according to the present embodiment will be shown in Experimental Examples 1 to 4 below.

 (実験例1)
 本発明は、水による燃焼反応という酸素を使用した燃焼反応とは異なる反応を利用し、改質を行うものである。本実験例1は、改質容器内で水による燃焼反応が発生することを明らかにする目的のため、実験途中においては有機性廃棄物、水を追加的に改質容器内に供給せず、改質容器内の気相部分において気体の発生状態を測定した。なお、本実験は既に反応定常工程に至った状態において、実験を開始したものである。
(Experimental example 1)
In the present invention, reforming is performed using a reaction different from a combustion reaction using oxygen, which is a combustion reaction using water. In this experimental example 1, organic waste and water are not additionally supplied into the reforming container during the experiment for the purpose of clarifying that the combustion reaction with water occurs in the reforming container. The gas generation state was measured in the gas phase part in the reforming vessel. In addition, this experiment started the experiment in the state which reached the reaction steady process already.

 有機性廃棄物として、籾殻20kgを使用し、改質容器に供給後、0.5リットルの水を籾殻に加えることで反応を開始した。本実験例における水には、安定同位体として酸素(18O)を含む同位体水H 18Oを10%濃度で用い、燃焼反応により生成する二酸化炭素量を測定する。なお、籾殻は約10重量%の含水量であった。 As organic waste, 20 kg of rice husk was used, and the reaction was started by adding 0.5 liter of water to the rice husk after supplying to the reforming vessel. For water in this experimental example, isotope water H 2 18 O containing oxygen ( 18 O) as a stable isotope is used at a concentration of 10%, and the amount of carbon dioxide generated by the combustion reaction is measured. The rice husk had a water content of about 10% by weight.

 表1は、改質容器内の二酸化炭素、酸素および窒素の測定結果をまとめたものである。0分、20分、41分、70分、180分と反応時間を設定し、改質容器内気相部分において気体の発生状態を、測定装置としてガスクロマトグラフおよびガスクロマトグラフ・マススペクトルを用いて測定した。反応開始から20分後には、18O を含む二酸化炭素(46CO)が発生することが示されている。同位体水H 18Oは、10%濃度で用いられており、反応開始から20分後には全二酸化炭素の内、約5.7%の 46COが発生している。ここから、発生した全二酸化炭素の約57%が加えた水0.5リットルの燃焼反応によって発生したことは明らかである。また、酸素は燃焼核の維持のための燃焼反応と、発生する水素が燃焼する際の反応に使用されたものと推察される。 Table 1 summarizes the measurement results of carbon dioxide, oxygen and nitrogen in the reforming vessel. The reaction time was set to 0 minutes, 20 minutes, 41 minutes, 70 minutes and 180 minutes, and the gas generation state in the gas phase part in the reforming container was measured using a gas chromatograph and a gas chromatograph mass spectrum as a measuring device. . Twenty minutes after the start of the reaction, it has been shown that carbon dioxide ( 46 CO 2 ) containing 18 O is generated. The isotope water H 2 18 O is used at a concentration of 10%, and 20 minutes after the start of the reaction, about 5.7% of 46 CO 2 is generated out of the total carbon dioxide. It is clear from this that about 57% of the total carbon dioxide evolved is generated by the combustion reaction of 0.5 liters of water added. Further, it is presumed that oxygen is used for the combustion reaction for maintaining the combustion nuclei and the reaction when the generated hydrogen is burned.

 さらに、注目すべきは、CO発生量がO減少量を上回っている点である。これは、酸素を使用した燃焼反応(図7(a)(b))のみでは起こり得ない現象であることから、この点からも水による燃焼反応が起こることが示された。 Furthermore, it should be noted that the amount of CO 2 generation exceeds the amount of O 2 reduction. This is a phenomenon that can not occur only by the combustion reaction using oxygen (Fig. 7 (a) and (b)), and it was shown from this point that the combustion reaction by water also occurs.

 (実験例2)
 次に、別の有機性廃棄物を用いて、本実施形態で行った別実験を以下に示す。本実験例2は、加水条件と非加水条件の違いによって改質容器内に発生する気体に与える影響を明らかにすることを目的とする。本実験は、実験例1同様、有機性廃棄物、水を追加的に改質容器内に供給せず、改質容器内の気相部分の状態を測定したものである。なお、本実験は、反応開始工程から実験を開始した。
(Experimental example 2)
Next, another experiment performed in this embodiment using another organic waste is shown below. The purpose of this experimental example 2 is to clarify the influence on the gas generated in the reforming vessel due to the difference between the hydrolysis condition and the non-hydrolysis condition. In this experiment, the organic waste and water were not additionally supplied into the reforming vessel as in Experimental Example 1, and the state of the gas phase in the reforming vessel was measured. In this experiment, the experiment was started from the reaction initiation step.

 有機性廃棄物として、塩化ビニル製のクロス紙10kgを使用し、改質容器に供給後、反応開始前に2リットルの水をクロス紙に加え、少量のカーバイドと水の反応により有機性廃棄物を着火させることで反応を開始させる。比較例として、水を供給しない非加水条件で同様に実験した例を示す。なお、クロス紙は約3重量%の含水量であった。 As organic waste, use 10 kg of vinyl chloride cloth paper and supply it to the reforming container, then add 2 liters of water to the cloth paper before the start of the reaction, and organic waste by reaction of a small amount of carbide and water. The reaction is started by igniting the As a comparative example, an example of the same experiment under non-hydrolytic conditions without water supply is shown. The cross paper had a water content of about 3% by weight.

 図8~図12は、0分、10分、30分、60分、90分、120分、150分、180分と反応時間を設定し、改質容器内気相部分において気体の発生状態を測定した測定結果を示すグラフである。測定装置としてガスクロマトグラフおよびガスクロマトグラフ・マススペクトルを用いて、気相部分に含まれる水素、一酸化炭素、二酸化炭素、酸素、窒素の量を測定した。グラフ縦軸は改質容器内気相部分の体積全体に対する割合を示したものである。 8 to 12 set the reaction time to 0 minutes, 10 minutes, 30 minutes, 60 minutes, 90 minutes, 120 minutes, 150 minutes, 180 minutes, and measure the gas generation state in the gas phase part in the reforming container It is a graph which shows the measured result. The amount of hydrogen, carbon monoxide, carbon dioxide, oxygen and nitrogen contained in the gas phase was measured using a gas chromatograph and a gas chromatograph mass spectrum as a measuring device. The vertical axis of the graph shows the ratio to the whole volume of the gas phase part in the reforming container.

 図8は実験例2において気相での水素の発生量を示すグラフである。非加水条件の比較例に比べ、加水状態のクロス紙からは水による燃焼反応により多量の水素ガスが容器内において発生していることを示している。なお、非加水条件の比較例においても、クロス紙に含まれる水、また酸素を使用した燃焼によって発生した水により、水による燃焼反応が起こることが推察される。 FIG. 8 is a graph showing the amount of hydrogen generation in the gas phase in Experimental Example 2. It shows that a large amount of hydrogen gas is generated in the container from the water-containing cross paper by the combustion reaction with water as compared with the comparative example under the non-hydrolytic condition. In addition, also in the comparative example of non-hydrolysis conditions, it is guessed that the combustion reaction by water will occur by the water contained by cloth and the water generated by combustion which used oxygen.

 図9は実験例2において気相での一酸化炭素の発生量を示すグラフである。非加水条件の比較例に比べ、加水状態のクロス紙からは水による燃焼反応により多量の一酸化炭素ガスが容器内において発生していることを示している。 FIG. 9 is a graph showing the amount of carbon monoxide generated in the gas phase in Experimental Example 2. It is shown that a large amount of carbon monoxide gas is generated in the container from the water-containing cross paper due to the combustion reaction with water as compared with the comparative example under the non-hydrolytic condition.

 図10は実験例2において気相での二酸化炭素の発生量を示すグラフである。非加水条件の比較例では、酸素を使用した燃焼反応によって二酸化炭素が発生するため、図9における非加水条件での一酸化炭素の発生割合と比べて、二酸化炭素の発生量が多いことが示されている。 FIG. 10 is a graph showing the amount of carbon dioxide generated in the gas phase in Experimental Example 2. In the comparative example of the non-hydrolytic condition, carbon dioxide is generated by the combustion reaction using oxygen, and therefore, it is shown that the generation amount of carbon dioxide is larger than the generation ratio of carbon monoxide under the non-hydrolytic condition in FIG. It is done.

 図11、12は実験例2において気相での酸素、窒素の量を示すグラフである。非加水条件に比べ、加水条件では、酸素、窒素とも減少していることが確認できる。これは、加水条件において発生する気体により、これらの割合が減少したものと推察される。 11 and 12 are graphs showing amounts of oxygen and nitrogen in the gas phase in Experimental Example 2. It can be confirmed that both the oxygen and the nitrogen are reduced under the hydrolysis condition as compared with the non-hydrolysis condition. It is presumed that this is due to the decrease of these proportions due to the gas generated under the water addition condition.

 (実験例3)
 本実験例3は、水素発生に最適な水分量を調べたものである。本実験は、実験例1および2同様、有機性廃棄物、水を追加的に改質容器内に供給せず、改質容器内の気相部分の状態を測定したものである。なお、本実験は、反応開始工程から実験を開始した。
(Experimental example 3)
In the present experimental example 3, the water content optimum for hydrogen generation was investigated. In this experiment, the organic waste and water were not additionally supplied into the reforming vessel as in Experimental Examples 1 and 2, and the state of the gas phase in the reforming vessel was measured. In this experiment, the experiment was started from the reaction initiation step.

 有機性廃棄物として、籾殻30kgを使用し、改質容器に供給後、反応開始前に4.5リットル、6.0リットル、12.0リットル、20.0リットル、30.0リットルと水分量を変え、それぞれ籾殻に加えておく。その後、少量のカーバイドと水の反応により有機性廃棄物を着火させ、反応を開始させる。なお、籾殻は約10重量%の含水量であった。 As organic waste, 30 kg of rice husk is used, and after supplying to the reforming vessel, before the start of the reaction, 4.5 liters, 6.0 liters, 12.0 liters, 20.0 liters, 30.0 liters and water content Change and add each to rice husk. The organic waste is then ignited by the reaction of a small amount of carbide with water to initiate the reaction. The rice husk had a water content of about 10% by weight.

 図13は、実験例3において気相での水素の発生量を示すグラフである。水素発生においては、籾殻30kgに対して水分量として20.0リットルの状態が最適であることが示された。 FIG. 13 is a graph showing the generation amount of hydrogen in the gas phase in Experimental Example 3. In hydrogen generation, it was shown that the condition of 20.0 liters as the amount of water was optimum for 30 kg of chaff.

 (実験例4)
 本実験例4は、有機性廃棄物の着火後から水素発生がなくなるまでの反応時間を測定した。本実験は、実験例1~3同様、有機性廃棄物、水を追加的に改質容器内に供給せず、改質容器内の気相部分の状態を測定したものである。なお、本実験は、反応開始工程から実験を開始した。
(Experimental example 4)
In this experimental example 4, the reaction time from the ignition of the organic waste to the disappearance of hydrogen was measured. This experiment, like the experimental examples 1 to 3, measures the state of the gas phase part in the reforming container without additionally supplying the organic waste and water into the reforming container. In this experiment, the experiment was started from the reaction initiation step.

 有機性廃棄物として、籾殻30kgを使用し、改質容器に供給後、反応開始前に20リットルの水を籾殻に加えた後、少量のカーバイドと水の反応により有機性廃棄物を着火させ、反応を開始させる。なお、籾殻は約10重量%の含水量であった。 After using 30 kg of rice husk as organic waste and supplying it to the reforming vessel, add 20 liters of water to the rice husk before starting the reaction, then ignite the organic waste by the reaction of a small amount of carbide and water, Start the reaction. The rice husk had a water content of about 10% by weight.

 図14は、実験例4において気相での水素の発生量を示すグラフである。630分でピークに達し、900分まで水素発生が継続していることが示されている。ピーク時点では体積比2.5%もの高濃度水素が発生することが示された。なお本実験は、本装置で籾殻30kgを改質させるために要する時間を示したものであり、反応定常工程において有機性廃棄物および水を補給すれば、改質反応が継続することは上述の通りである。本実験では、最終時点(900分)で籾殻はほぼ全て改質され、改質残渣が残るのみであった。 FIG. 14 is a graph showing the generation amount of hydrogen in the gas phase in Experimental Example 4. The peak is reached at 630 minutes, and it is shown that hydrogen generation continues up to 900 minutes. It was shown that as high as 2.5% by volume of hydrogen was generated at the peak time. Note that this experiment shows the time required to reform 30 kg of rice husks with this apparatus, and if the organic waste and water are replenished in the reaction steady process, the reforming reaction continues as described above. It is street. In this experiment, almost all the rice husk was reformed at the final time (900 minutes), and only the reforming residue remained.

 上記実験結果から、本発明における有機性廃棄物を改質する方法では、外部からのエネルギーを使用せずに有機性廃棄物を改質することが可能であることは明らかである。また改質によって生成するガスは高濃度水素を含有するため、これを回収し水素ガスとして利用できること、また有機性廃棄物の種類によっては、生成した改質残渣を肥料として利用することが可能である。 From the above experimental results, it is clear that in the method of reforming organic waste according to the present invention, it is possible to reform organic waste without using external energy. Also, since the gas produced by reforming contains high concentration hydrogen, it can be recovered and used as hydrogen gas, and depending on the type of organic waste, it is possible to use the produced reforming residue as fertilizer is there.

 本発明は、外部からのエネルギーを使用せずに有機物を改質する方法、およびその改質方法を実現するための、有機性廃棄物改質用装置に関するものである。改質によって生成するガスは高濃度水素を含有しており、これを回収し水素ガスとして利用することができ、有機性廃棄物の種類によっては、生成した改質残渣を肥料として利用することが可能であることから、産業上の利用可能性は極めて高い。 The present invention relates to a method of reforming organic matter without using external energy, and an organic waste reforming apparatus for realizing the reforming method. The gas produced by reforming contains high concentration hydrogen, which can be recovered and used as hydrogen gas, and depending on the type of organic waste, utilizing the produced reforming residue as fertilizer Since it is possible, industrial applicability is extremely high.

 S1  反応開始工程
 S2  反応拡大工程
 S3  反応定常工程
 10  有機性廃棄物改質用装置
 11  改質容器
 12  容器壁
 12a 天井部
 12b 周壁部
 12c 底部
 13  供給手段
 13a 供給口
 13b 供給口蓋体
 14  穿設孔
 15  有機性廃棄物
 16  脚部
 17  改質残渣
 18  改質容器内
 19  排出口
 20  給水手段
 20a 給水タンク
 20b シャワー部
 21  排出ガス処理手段
 21a 通気筒体
 21b ガス捕集部
 21c タール除去部
 21d 吸引ファン
 22  温度センサー
 22a 温度検知部位
 22b 本体
 22c 表示部
 23  気体導入管
 23a 気体導入口
 24  燃焼核
 25  燃焼核周辺部
S1 Reaction start process S2 Reaction expansion process S3 Reaction steady process 10 Apparatus for reforming organic waste 11 Reforming container 12 Container wall 12a Ceiling part 12b Ceiling part 12c Bottom part 13 Supply means 13a Supply port 13b Supply port cover 14 Drill hole DESCRIPTION OF SYMBOLS 15 Organic waste 16 leg part 17 Reforming residue 18 Reforming container inside 19 Discharge port 20 Water supply means 20a Water supply tank 20b Shower part 21 Exhaust gas processing means 21a Air cylinder 21b Gas collection part 21c Tar removal part 21d Suction fan 22 temperature sensor 22a temperature detection part 22b main body 22c display part 23 gas introduction pipe 23a gas introduction port 24 combustion nucleus 25 combustion nucleus peripheral part

Claims (6)

有機性廃棄物を改質容器内に供給し、反応開始剤を用いて有機性廃棄物の一部において改質を開始する反応開始工程と、
気体導入管による改質容器内への通気と、水による燃焼反応を行うための給水により反応を拡大させる反応拡大工程と、
燃焼核の大きさを維持することにより改質を定常的に行う反応定常工程と、
を有し、高濃度水素ガスの発生を伴うことを特徴とする有機性廃棄物の改質方法。
A reaction initiation step of feeding organic waste into a reforming vessel and initiating reforming of a portion of the organic waste using a reaction initiator;
A reaction expansion step of expanding the reaction by aeration into the reforming container with a gas introduction pipe and water supply for performing a combustion reaction with water;
A steady-state reaction step in which reforming is performed in a steady manner by maintaining the size of combustion nuclei;
A method of reforming organic waste, comprising: generating hydrogen gas with high concentration.
前記反応開始工程は、前記反応開始剤として少量のカーバイドと水とを用いて有機性廃棄物の一部を着火させる工程を有する、請求項1に記載の有機性廃棄物の改質方法。 The method for reforming organic waste according to claim 1, wherein the reaction initiation step comprises the step of igniting a part of the organic waste using a small amount of carbide and water as the reaction initiator. 前記反応拡大工程における改質容器内への通気は、気体導入管による改質容器内への外気の導入を調整することを特徴とする請求項1または請求項2に記載の有機性廃棄物の改質方法。 The organic waste according to claim 1 or 2, wherein the aeration into the reforming container in the reaction expansion step adjusts the introduction of the outside air into the reforming container by the gas introduction pipe. Reforming method. 前記反応拡大工程における給水は、給水手段により外部より水を連続的に補充することを特徴とする請求項1~3に記載の有機性廃棄物の改質方法。 The method for reforming organic waste according to any one of claims 1 to 3, wherein water supply in the reaction expansion step is continuously replenished with water from the outside by a water supply means. 前記反応定常工程における燃焼核の大きさの維持は、温度センサーを用いた温度検知を基に、前記気体導入管による改質容器内への通気と、前記改質容器内への前記給水を調整することにより行うことを特徴とする請求項1~4に記載の有機性廃棄物の改質方法。 The maintenance of the size of the combustion core in the reaction steady process adjusts the aeration into the reforming container by the gas introduction pipe and the water supply into the reforming container based on temperature detection using a temperature sensor The method for reforming organic waste according to any one of claims 1 to 4, which is carried out by 有機性廃棄物の供給手段と、
供給手段から供給された有機性廃棄物の改質を行う改質容器と、
有機性廃棄物の燃焼中における温度状態を把握するための温度センサーと、
改質容器内への通気を行うための気体導入管と、
改質を行うため水を補充する給水手段と、
改質が行われた改質残渣を外部に排出する排出手段と、
前記改質容器から排出するガスを処理する排出ガス処理手段と、
を有し、高濃度水素ガスの発生を伴うことを特徴とする有機性廃棄物改質用装置。
Means for supplying organic waste,
A reforming vessel for reforming organic waste supplied from the supply means;
A temperature sensor for grasping the temperature condition during combustion of organic waste,
A gas introduction pipe for ventilating the inside of the reforming vessel;
Water supply means for replenishing water to perform reforming;
An exhausting means for discharging the reformed reforming residue to the outside;
Exhaust gas processing means for processing the gas discharged from the reforming container;
An apparatus for reforming organic waste, comprising: generating hydrogen gas with high concentration.
PCT/JP2009/006784 2009-12-11 2009-12-11 Method of organic-waste modification accompanied by generation of high-concentration hydrogen gas and device for modifying organic waste Ceased WO2011070624A1 (en)

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04367502A (en) * 1991-01-28 1992-12-18 Mitsubishi Heavy Ind Ltd Production of synthetic gas
JPH0711260A (en) * 1993-04-15 1995-01-13 Jii R:Kk Water gas generator
JPH11100583A (en) * 1997-07-30 1999-04-13 Noel Krc Energ & Umwelttechnik Gmbh Process for gasifying compressed or compressible organic material and apparatus therefor
JP2002235090A (en) * 2001-02-09 2002-08-23 Mitsubishi Heavy Ind Ltd Method for gasifying biomass and gasifier therefor, and method and equipment for producing methanol

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04367502A (en) * 1991-01-28 1992-12-18 Mitsubishi Heavy Ind Ltd Production of synthetic gas
JPH0711260A (en) * 1993-04-15 1995-01-13 Jii R:Kk Water gas generator
JPH11100583A (en) * 1997-07-30 1999-04-13 Noel Krc Energ & Umwelttechnik Gmbh Process for gasifying compressed or compressible organic material and apparatus therefor
JP2002235090A (en) * 2001-02-09 2002-08-23 Mitsubishi Heavy Ind Ltd Method for gasifying biomass and gasifier therefor, and method and equipment for producing methanol

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