WO2011048685A1 - Hydrogen generating agent, hydrogen generating method employing said generating agent, and hydrogen generating apparatus - Google Patents

Hydrogen generating agent, hydrogen generating method employing said generating agent, and hydrogen generating apparatus Download PDF

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WO2011048685A1
WO2011048685A1 PCT/JP2009/068191 JP2009068191W WO2011048685A1 WO 2011048685 A1 WO2011048685 A1 WO 2011048685A1 JP 2009068191 W JP2009068191 W JP 2009068191W WO 2011048685 A1 WO2011048685 A1 WO 2011048685A1
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hydrogen
water
powder
activated carbon
container
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PCT/JP2009/068191
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French (fr)
Japanese (ja)
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初男 小柳津
一之 平尾
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株式会社テラウィング
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Priority to PCT/JP2009/068191 priority Critical patent/WO2011048685A1/en
Priority to JP2011534439A priority patent/JP4846075B2/en
Publication of WO2011048685A1 publication Critical patent/WO2011048685A1/en

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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/06Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of inorganic compounds containing electro-positively bound hydrogen, e.g. water, acids, bases, ammonia, with inorganic reducing agents
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/30Active carbon
    • C01B32/312Preparation
    • C01B32/318Preparation characterised by the starting materials
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B33/00Silicon; Compounds thereof
    • C01B33/06Metal silicides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B39/00Compounds having molecular sieve and base-exchange properties, e.g. crystalline zeolites; Their preparation; After-treatment, e.g. ion-exchange or dealumination
    • C01B39/02Crystalline aluminosilicate zeolites; Isomorphous compounds thereof; Direct preparation thereof; Preparation thereof starting from a reaction mixture containing a crystalline zeolite of another type, or from preformed reactants; After-treatment thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/36Hydrogen production from non-carbon containing sources, e.g. by water electrolysis

Definitions

  • the present invention relates to a hydrogen generator capable of generating hydrogen when immersed in water, and a hydrogen generation method and a hydrogen generator using the hydrogen generator.
  • hydrogen has characteristics such as being colorless and odorless, having a high combustion temperature of 3000 ° C., and generating no carbon dioxide or harmful gas even when burned. Consideration of using it as a new energy source is underway. However, hydrogen as an energy source has not been practically used because its production cost is high.
  • Patent Documents 1 to 3 As conventional methods for generating hydrogen from water without using fossil fuels, for example, those described in Patent Documents 1 to 3 are known.
  • Patent Document 1 discloses a method in which a new surface not covered with an oxide film is generated by cutting / grinding aluminum or an aluminum alloy in water at room temperature, and hydrogen is generated by reacting the new surface with water. It is disclosed.
  • Patent Document 2 discloses a method for generating hydrogen by reacting aluminum powder or a mixed powder composed of aluminum powder and metal powder (for example, zinc powder) having a smaller ionization tendency than aluminum and water. Yes.
  • Patent Document 3 discloses a hydrogen generator composed of aluminum powder and calcium oxide powder. When this hydrogen generating agent is immersed in water, calcium oxide and water react to produce calcium hydroxide, and this calcium hydroxide and aluminum powder react to generate hydrogen.
  • Patent Document 1 cannot generate a large amount of hydrogen because sufficient reaction rate cannot be obtained unless water is heated from the outside.
  • Patent Document 2 since the method described in Patent Document 2 requires a thermal spraying device for obtaining aluminum powder or zinc-aluminum powder, enlargement and complexity of the device are inevitable, and hydrogen can be generated at low cost. There wasn't.
  • the hydrogen generating agent described in Patent Document 3 could not generate hydrogen in an amount that can be used as an energy source. Specifically, the amount of hydrogen that can be generated by this hydrogen generating agent can only generate electric power necessary for driving a mobile phone.
  • the present invention has been made in view of such circumstances, and the object of the present invention is to provide a hydrogen generator capable of generating hydrogen in a large amount at a low cost, and a hydrogen generation method using the hydrogen generator. And providing a hydrogen generator.
  • a hydrogen generator generates hydrogen when immersed in water, and (1) a zeolite powder containing at least Al, Si and an alkali metal and a calcium compound powder (2) activated carbon powder having a large number of micropores and a specific surface area of 1000 m 2 / g or more, and (3) ⁇ -iron silicide, and 100 parts by weight of the mixed powder. Then, the activated carbon powder and the ⁇ iron silicide are each 0.1 parts by weight or more.
  • the hydrogen generator further contains 0.1 parts by weight or more of a magnesium compound
  • the activated carbon powder is selected from cedar thinned wood, coconut husk, diatomaceous earth, flowers, sawdust, tofu cake, rice husk and rice bran It is preferable to carbonize at least one plant material prepared.
  • the hydrogen generation method according to the present invention is a method using the hydrogen generator, and the powdery ⁇ -iron silicide is combined with at least the mixed powder and the activated carbon powder. It is characterized by being immersed in water and immersed.
  • another hydrogen generation method is a method using the above-mentioned hydrogen generating agent, wherein the ⁇ iron silicide is disposed on the inner surface in advance.
  • the water is stored, and at least the mixed powder and the activated carbon powder are put into the stored water and immersed therein.
  • a hydrogen generator generates hydrogen using the hydrogen generation method, and includes a container for storing water, at least the mixed powder, and the An inlet for charging activated carbon powder into the container, water temperature measuring means for measuring the temperature of the water stored in the container, and water volume measurement for measuring the amount of water stored in the container And a water injection means for injecting the water based on the measurement result of the water temperature measurement means and / or the water amount measurement means, and a hydrogen outlet for taking out the generated hydrogen.
  • the present invention it is possible to provide a hydrogen generating agent capable of generating a large amount of hydrogen at a low cost, and a hydrogen generating method and a hydrogen generating apparatus using the hydrogen generating agent. Further, according to the present invention, since it is not necessary to burn fossil fuel, hydrogen can be generated without placing a burden on the global environment.
  • the measurement results of the total hydrogen generation amount (A) to (C) are graphs showing the transition of the total hydrogen generation amount for 120 minutes, 48 hours, and 5 days, respectively.
  • FIG. 5 is a graph showing the hydrogen generation amount measurement results for each predetermined time, wherein (A) to (C) are graphs showing the generation amount every 5 minutes, every 2 hours, and every day. It is a schematic diagram for demonstrating the structure of the hydrogen generator which concerns on this invention.
  • the hydrogen generator according to the present invention generates hydrogen when immersed in water.
  • the mixed powder composed of zeolite powder and calcium compound powder is mixed with activated carbon powder, ⁇ -iron silicide ( ⁇ -FeSi 2 ), Is added.
  • ⁇ -FeSi 2 ⁇ -iron silicide
  • the hydrogen generator has a powder form as a whole, it can be stored and handled easily by forming it into a pellet or tablet by pressing.
  • Zeolite powder is a variety of zeolites containing a small amount of strontium, rubidium, barium, zinc, sulfur, molybdenum, etc. in addition to silicon, aluminum, iron, magnesium, calcium, sodium, potassium, phosphorus, manganese, titanium dioxide, etc. , which are naturally produced including at least aluminum, silicon and alkali metals (eg, Mg, Rb, etc.).
  • mordenite-type zeolite, A-type zeolite, dolomite powder, or artificial zeolite powder obtained by processing slaked lime can also be used as the zeolite powder.
  • the calcium powder is, for example, calcium hydroxide (Ca (OH) 2 ) or calcium carbonate (CaCO 3 ).
  • Calcium carbonate powder can be obtained very inexpensively by washing, crushing, and sun-drying various oyster, scallop or pearl shells.
  • the content of zeolite powder is preferably about 40 to 70 parts by weight, and the content of calcium powder is about 50 to 60 parts by weight. Is preferred.
  • the content of the zeolite powder is less than 30 parts by weight, the generation amount of hydrogen is lowered and productivity is lowered. This is thought to be because too little zeolite powder contributes to the hydrogen generation reaction described later.
  • the rate of the hydrogen generation reaction described later is lowered, and the productivity is lowered.
  • the content of the calcium powder exceeds 62 parts by weight, unreacted calcium is included in the generated hydrogen, and calcium adheres to the inside of a pipe or the like for transporting the generated hydrogen, which is not preferable.
  • the activated carbon powder is carbonized vegetable material. Specifically, the activated carbon powder is carbonized in a furnace at 400-800 ° C, which is cheap and readily available, such as cedar thinned wood, coconut husk, diatomaceous earth, grass, flowers, sawdust, tofu lees, rice husks, rice bran. As a result, the charcoal was produced, and further, this charcoal was produced by heat treatment for a predetermined time (temperature: 400-800 ° C., time: 60-360 minutes) in a vacuum state of about 10 ⁇ 1 Pa to 10 ⁇ 5 Pa. Is.
  • the activated carbon powder has a high carbon quality with a carbonization rate of 90% or more and a pH of 9.0 to 11.0. In addition, a large number of fine pores having a diameter of about 3 nm are formed on the surface of the activated carbon powder, and the specific surface area is 1000 m 2 / g or more.
  • the activated carbon powder has various fullerene shapes such as a soccer ball type, a carbon nanotube type, a bucky onion type, and a horn type.
  • ⁇ -iron silicide is a kind of so-called environmental semiconductor composed of elements that have a high Clarke number and are not toxic to the human body, and is known to emit electromagnetic waves in the band of several milliHz to several teraHz at room temperature. Yes.
  • ⁇ -iron silicide can be powdered and added to the mixed powder together with the activated carbon powder.
  • the addition amount of ⁇ iron silicide and activated carbon powder may be 0.1 parts by weight or more. That is, it becomes a hydrogen generator capable of generating a large amount of hydrogen over a long period of time by adding a small amount of ⁇ -iron silicide and activated carbon powder to the mixed powder by a hydrogen generation reaction described later.
  • ⁇ -iron silicide can be dispersed in a phenolic resin and placed at the bottom of a container for storing water to be used for the hydrogen generation reaction, or can be slurried and applied to the inside of the container. Even in this case, ⁇ -iron silicide can contribute to the hydrogen generation reaction described later.
  • immersion in the specification and claims of this application not only applies a hydrogen generating agent to stored water but also pre-applies ⁇ iron silicide constituting the hydrogen generating agent. It shall also include storing water in a previously prepared container.
  • the present invention by adding activated carbon powder and ⁇ -iron silicide to a mixed powder composed of zeolite powder and calcium compound powder, the known hydrogen generation reaction is promoted, and a large amount of hydrogen is generated in a short time. Hydrogen can be generated over a long period of time.
  • the hydrogen generating agent according to the first embodiment the mixed powder consisting of a zeolite powder 48g calcium hydroxide powder 50 g, cedar thinnings carbide or the like to give specific surface area 1000 m 2 / g or more 1 g of activated carbon powder and 1 g of ⁇ iron silicide powder were added to make a total of 100 g.
  • the hydrogen generator according to Example 2 is obtained by further adding 1 g of magnesium silicide (MgSi 2 ) powder to the hydrogen generator according to Example 1 to obtain 47 g of zeolite powder.
  • the hydrogen generator according to the conventional example is obtained by adding 49 g of zeolite powder without adding ⁇ -iron silicide.
  • each hydrogen generating agent was immersed in 500 ml of water stored in the glass container, and the amount of hydrogen generation for every fixed time was measured with the flow meter.
  • the water amount is maintained in the range of 45 to 90 ° C. by appropriately replenishing water, and the water amount is 300 ml. It was made not to fall below.
  • a large amount of hydrogen can be generated immediately after the start of the experiment. it can.
  • the total amount of hydrogen generated after 30 minutes is 180 L in the conventional example (*), but 1332 L in the first example and 1607 L in the second example.
  • the hydrogen generating agent according to the conventional example hardly generates hydrogen after about 24 hours (particularly, refer to FIG. 2B).
  • the hydrogen generating agent according to Example 1 and Example 2 at least 5 days pass even after 24 hours. Until then, a substantially constant amount of hydrogen can continue to be generated.
  • Example 2 Compared Example 1 and Example 2, Example 2 to which magnesium silicide was further added had a larger amount of hydrogen generation for about 90 minutes immediately after the start of the experiment. This is presumably because magnesium silicide further promoted the hydrogen generation reaction. In addition, it was confirmed that the amount of hydrogen generation increased when magnesium oxide (MgO) was added instead of magnesium silicide as compared with the conventional type.
  • MgO magnesium oxide
  • the hydrogen generator 1 introduces a hydrogen generating agent into a container 2 composed of a glass container body 2 a and a lid 2 b that seals the container body 2 a. And a water inlet 7 for taking out the generated hydrogen out of the container 2 and a water injection means 6 for storing water in the container 2.
  • the hydrogen generator 1 includes a water temperature measuring unit 4 for measuring the temperature of the water 8 stored in the container 2 and a water amount measuring unit 5 for measuring the amount of the water 8. Signals output from the water temperature measuring means 4 and the water amount measuring means 5 are input to the water injection means 6.
  • the water temperature measuring means 4 measures the temperature of the water 8 and the water amount measuring means 5 measures the amount of the water 8. Then, the water temperature measuring means 4 and the water amount measuring means 5 each output a signal corresponding to the measurement result.
  • the water injection means 6 replenishes the container 2 with an appropriate amount of new water. Thereby, it is prevented that the water temperature becomes too high or the water becomes too low.
  • the hydrogen generator 1 since the adjustment of the water temperature and the amount of water after the generation of hydrogen is automated and takes less time, the production cost of hydrogen can be reduced.
  • water is replenished based on both the water temperature and the amount of water, but may be replenished based on only one of them.
  • various kinds of natural and artificial zeolite powders, calcium compound powders other than calcium hydroxide, and activated carbon powders made of plant materials other than cedar thinning materials the same hydrogen generation effect as described above can be obtained.
  • the water in which the hydrogen generating agent is immersed is not limited to pure water, and even when tap water or seawater is used, the same hydrogen generating effect as described above can be obtained.

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Abstract

Disclosed are a hydrogen generating agent, a hydrogen generating method employing said hydrogen generating agent, and a hydrogen generating apparatus which can generate hydrogen cheaply and in large quantities. The hydrogen generating agent generates hydrogen when immersed in water, and includes 1) a mixed powder comprising a powdered calcium compound and a zeolite powder which contains at least Al, Si, and an alkali metal; 2) activated charcoal powder with numerous micropores and with a surface to volume ratio of 1000m2/g or more; 3) and β-iron silicide. The hydrogen generating agent is characterized by having at least 0.1 parts by weight each of the activated charcoal powder and the β-iron silicide for every 100 parts of the mixed powder.

Description

水素発生剤、並びに該発生剤を用いた水素発生方法および水素発生装置HYDROGEN GENERATOR, HYDROGEN GENERATION METHOD AND HYDROGEN GENERATOR USING THE GENERATOR
 本発明は、水に浸漬させると水素を発生させることができる水素発生剤、並びにこの水素発生剤を用いた水素発生方法および水素発生装置に関する。 The present invention relates to a hydrogen generator capable of generating hydrogen when immersed in water, and a hydrogen generation method and a hydrogen generator using the hydrogen generator.
 現在、世界では推定年間5000億Nm以上の水素が製造されている。そして、このうちの97%は化石燃料を燃焼させることにより製造され、残りは水を電気分解等することにより製造されている。製造された水素は、アンモニアやメタノール等の化学合成や、石油精製の分野で広く使用されている。 Currently, the world's estimated annual 500 billion Nm 3 or more of the hydrogen is produced. Of these, 97% is produced by burning fossil fuel, and the rest is produced by electrolyzing water. The produced hydrogen is widely used in the fields of chemical synthesis such as ammonia and methanol, and petroleum refining.
 また、水素は、無色・無臭であること、燃焼温度が3000℃と高いこと、燃焼しても二酸化炭素や有害なガスを発生しないこと等の特徴を有していることから、特に近年はクリーンなエネルギー源として活用することの検討が進められている。しかしながら、エネルギー源としての水素は、その製造コストが高価であることから実用化があまり進んでいない。 In addition, hydrogen has characteristics such as being colorless and odorless, having a high combustion temperature of 3000 ° C., and generating no carbon dioxide or harmful gas even when burned. Consideration of using it as a new energy source is underway. However, hydrogen as an energy source has not been practically used because its production cost is high.
 上記のように、水素の発生方法には、化石燃料を燃焼させる方法と水を電気分解等させる方法とがあるが、前者は大量の二酸化炭素を排出するので地球環境の面で問題がある。このため、水素をクリーンなエネルギー源として活用していくためには、化石燃料に頼らないで、安価に、しかも大量に水素を発生させる方法を見つけ出す必要がある。 As described above, there are two methods for generating hydrogen, namely, a method of burning fossil fuel and a method of electrolyzing water, but the former has a problem in terms of the global environment because it emits a large amount of carbon dioxide. For this reason, in order to use hydrogen as a clean energy source, it is necessary to find a method for generating hydrogen in a large amount at a low cost without relying on fossil fuels.
 化石燃料を使用せずに水から水素を発生させる従来の方法としては、例えば、特許文献1~3に記載のものが知られている。 As conventional methods for generating hydrogen from water without using fossil fuels, for example, those described in Patent Documents 1 to 3 are known.
 特許文献1には、常温の水中でアルミニウムまたはアルミニウム合金を切削/研削加工することにより酸化膜に覆われていない新生面を生成し、その新生面と水とを反応させることにより水素を発生させる方法が開示されている。 Patent Document 1 discloses a method in which a new surface not covered with an oxide film is generated by cutting / grinding aluminum or an aluminum alloy in water at room temperature, and hydrogen is generated by reacting the new surface with water. It is disclosed.
 特許文献2には、アルミニウム粉末、またはアルミニウム粉末およびアルミニウムよりもイオン化傾向の小さい金属粉末(例えば、亜鉛粉末)からなる混合粉末と水とを反応させることにより、水素を発生させる方法が開示されている。 Patent Document 2 discloses a method for generating hydrogen by reacting aluminum powder or a mixed powder composed of aluminum powder and metal powder (for example, zinc powder) having a smaller ionization tendency than aluminum and water. Yes.
 また、特許文献3には、アルミニウム粉末と酸化カルシウム粉末とからなる水素発生剤が開示されている。この水素発生剤を水に浸漬させると、酸化カルシウムと水とが反応して水酸化カルシウムが生成され、さらにこの水酸化カルシウムとアルミニウム粉末が反応して水素が発生する。 Patent Document 3 discloses a hydrogen generator composed of aluminum powder and calcium oxide powder. When this hydrogen generating agent is immersed in water, calcium oxide and water react to produce calcium hydroxide, and this calcium hydroxide and aluminum powder react to generate hydrogen.
特開2001-31401号公報Japanese Patent Laid-Open No. 2001-3401 特開2002-104801号公報JP 2002-104801 A 特開2004-231466号公報JP 2004-231466 A
 しかしながら、特許文献1に記載の方法では、水を外部から加熱しないと十分な反応速度が得られないため、水素を大量に発生させることはできなかった。 However, the method described in Patent Document 1 cannot generate a large amount of hydrogen because sufficient reaction rate cannot be obtained unless water is heated from the outside.
 また、特許文献2に記載の方法は、アルミニウム粉末または亜鉛アルミニウム粉末を得るための溶射装置を必要とするので、装置の大型化、複雑化が避けられず、安価に水素を発生させることはできなかった。 Moreover, since the method described in Patent Document 2 requires a thermal spraying device for obtaining aluminum powder or zinc-aluminum powder, enlargement and complexity of the device are inevitable, and hydrogen can be generated at low cost. There wasn't.
 さらに、特許文献3に記載の水素発生剤では、エネルギー源として使用できる程度の量の水素を発生させることはできなかった。具体的には、この水素発生剤で発生することはできる量の水素では、携帯電話の駆動に必要となる電力しか発生させることができなかった。 Furthermore, the hydrogen generating agent described in Patent Document 3 could not generate hydrogen in an amount that can be used as an energy source. Specifically, the amount of hydrogen that can be generated by this hydrogen generating agent can only generate electric power necessary for driving a mobile phone.
 本発明はこのような事情を鑑みてなされたものであって、その目的とするところは、安価かつ大量に水素を発生させることができる水素発生剤、並びにこの水素発生剤を用いた水素発生方法および水素発生装置を提供することにある。 The present invention has been made in view of such circumstances, and the object of the present invention is to provide a hydrogen generator capable of generating hydrogen in a large amount at a low cost, and a hydrogen generation method using the hydrogen generator. And providing a hydrogen generator.
 上記課題を解決するために、本発明に係る水素発生剤は、水に浸漬されると水素を発生させるものであって、(1)Al、Siおよびアルカリ金属を少なくとも含むゼオライト粉末とカルシウム化合物粉末とからなる混合粉末と、(2)多数の微細孔を有し、比表面積が1000m/g以上である活性炭粉末と、(3)β鉄シリサイドとを含み、前記混合粉末を100重量部とすると、前記活性炭粉末および前記β鉄シリサイドはそれぞれ0.1重量部以上であることを特徴とする。 In order to solve the above problems, a hydrogen generator according to the present invention generates hydrogen when immersed in water, and (1) a zeolite powder containing at least Al, Si and an alkali metal and a calcium compound powder (2) activated carbon powder having a large number of micropores and a specific surface area of 1000 m 2 / g or more, and (3) β-iron silicide, and 100 parts by weight of the mixed powder. Then, the activated carbon powder and the β iron silicide are each 0.1 parts by weight or more.
 上記水素発生剤は、さらに0.1重量部以上のマグネシウム化合物を含むことが好ましく、さらに前記活性炭粉末は、杉間伐材、やし殻、珪藻土、草花、おが屑、豆腐粕、籾殻および米ぬかから選択された少なくとも1種類の植物性材料を炭化させたものであることが好ましい。 It is preferable that the hydrogen generator further contains 0.1 parts by weight or more of a magnesium compound, and the activated carbon powder is selected from cedar thinned wood, coconut husk, diatomaceous earth, flowers, sawdust, tofu cake, rice husk and rice bran It is preferable to carbonize at least one plant material prepared.
 また、上記課題を解決するために、本発明に係る水素発生方法は、上記水素発生剤を用いた方法であって、粉末状の前記β鉄シリサイドを、少なくとも前記混合粉末および前記活性炭粉末とともに前記水に投入して浸漬させることを特徴とする。 Further, in order to solve the above-mentioned problem, the hydrogen generation method according to the present invention is a method using the hydrogen generator, and the powdery β-iron silicide is combined with at least the mixed powder and the activated carbon powder. It is characterized by being immersed in water and immersed.
 また、上記課題を解決するために、本発明に係るもうひとつの水素発生方法は、上記水素発生剤を用いた方法であって、内表面に前記β鉄シリサイドをあらかじめ配しておいた容器に前記水を貯留し、貯留された前記水に少なくとも前記混合粉末および前記活性炭粉末を投入して浸漬させることを特徴とする。 In order to solve the above-mentioned problem, another hydrogen generation method according to the present invention is a method using the above-mentioned hydrogen generating agent, wherein the β iron silicide is disposed on the inner surface in advance. The water is stored, and at least the mixed powder and the activated carbon powder are put into the stored water and immersed therein.
 また、上記課題を解決するために、本発明に係る水素発生装置は、上記水素発生方法を用いて水素を発生させるものであって、水を貯留するための容器と、少なくとも前記混合粉末および前記活性炭粉末を前記容器内に投入するための投入口と、前記容器に貯留されている前記水の温度を測定する水温測定手段と、前記容器に貯留されている前記水の量を測定する水量測定手段と、前記水温測定手段および/または前記水量測定手段の測定結果に基づいて、前記水を注入する水注入手段と、発生した水素を取り出すための水素取出口とを備えたことを特徴とする。 In order to solve the above problems, a hydrogen generator according to the present invention generates hydrogen using the hydrogen generation method, and includes a container for storing water, at least the mixed powder, and the An inlet for charging activated carbon powder into the container, water temperature measuring means for measuring the temperature of the water stored in the container, and water volume measurement for measuring the amount of water stored in the container And a water injection means for injecting the water based on the measurement result of the water temperature measurement means and / or the water amount measurement means, and a hydrogen outlet for taking out the generated hydrogen. .
 本発明によれば、安価かつ大量に水素を発生させることができる水素発生剤、並びにこの水素発生剤を用いた水素発生方法および水素発生装置を提供することができる。また、本発明によれば、化石燃料を燃焼させる必要がないので、地球環境に負担をかけることなく水素を発生させることができる。 According to the present invention, it is possible to provide a hydrogen generating agent capable of generating a large amount of hydrogen at a low cost, and a hydrogen generating method and a hydrogen generating apparatus using the hydrogen generating agent. Further, according to the present invention, since it is not necessary to burn fossil fuel, hydrogen can be generated without placing a burden on the global environment.
水素総発生量の測定結果であって、(A)~(C)はそれぞれ120分間、48時間、5日間の総発生量の推移を示すグラフである。The measurement results of the total hydrogen generation amount (A) to (C) are graphs showing the transition of the total hydrogen generation amount for 120 minutes, 48 hours, and 5 days, respectively. 所定時間毎の水素発生量の測定結果であって、(A)~(C)はそれぞれ5分毎、2時間毎、1日毎の発生量を示すグラフである。FIG. 5 is a graph showing the hydrogen generation amount measurement results for each predetermined time, wherein (A) to (C) are graphs showing the generation amount every 5 minutes, every 2 hours, and every day. 本発明に係る水素発生装置の構成を説明するための模式図である。It is a schematic diagram for demonstrating the structure of the hydrogen generator which concerns on this invention.
[水素発生剤、水素発生方法]
 以下、図1および図2に示す実験結果を参照しながら、本発明に係る水素発生剤および水素発生方法の好ましい実施形態について説明する。
[Hydrogen generating agent, hydrogen generating method]
Hereinafter, preferred embodiments of the hydrogen generating agent and the hydrogen generating method according to the present invention will be described with reference to the experimental results shown in FIGS. 1 and 2.
 本発明に係る水素発生剤は、水に浸漬されると水素を発生させるものであって、ゼオライト粉末およびカルシウム化合物粉末からなる混合粉末に、活性炭粉末と、β鉄シリサイド(β-FeSi)とを添加してなる。水素発生剤は、全体としても粉末状を有しているが、プレス加工で成形してペレット状やタブレット状にすれば保存や取り扱いが容易になる。 The hydrogen generator according to the present invention generates hydrogen when immersed in water. The mixed powder composed of zeolite powder and calcium compound powder is mixed with activated carbon powder, β-iron silicide (β-FeSi 2 ), Is added. Although the hydrogen generator has a powder form as a whole, it can be stored and handled easily by forming it into a pellet or tablet by pressing.
 ゼオライト粉末は、ケイ素、アルミニウム、鉄、マグネシウム、カルシウム、ナトリウム、カリウム、リン、マンガン、二酸化チタン等の他、微量のストロンチウム、ルビジウム、バリウム、亜鉛、硫黄、モリブデン等を含む種々のゼオライトのうちの、少なくともアルミニウム、ケイ素およびアルカリ金属(例えば、Mg、Rb等)を含む天然に産出されるものである。本発明では、例えば、モルデナイト型のゼオライト、A型ゼオライト、ドロマイトの粉末、または消石灰を加工した人工ゼオライト粉末もゼオライト粉末として使用することができる。 Zeolite powder is a variety of zeolites containing a small amount of strontium, rubidium, barium, zinc, sulfur, molybdenum, etc. in addition to silicon, aluminum, iron, magnesium, calcium, sodium, potassium, phosphorus, manganese, titanium dioxide, etc. , Which are naturally produced including at least aluminum, silicon and alkali metals (eg, Mg, Rb, etc.). In the present invention, for example, mordenite-type zeolite, A-type zeolite, dolomite powder, or artificial zeolite powder obtained by processing slaked lime can also be used as the zeolite powder.
 カルシウム粉末は、例えば、水酸化カルシウム(Ca(OH))、炭酸カルシウム(CaCO)の粉末である。炭酸カルシウムの粉末は、牡蠣、ホタテまたは真珠の各種貝殻を洗浄、粉砕、および天日干しすることにより、非常に安価に入手することができる。 The calcium powder is, for example, calcium hydroxide (Ca (OH) 2 ) or calcium carbonate (CaCO 3 ). Calcium carbonate powder can be obtained very inexpensively by washing, crushing, and sun-drying various oyster, scallop or pearl shells.
 ゼオライト粉末およびカルシウム化合物粉末からなる混合粉末を100重量部とすると、ゼオライト粉末の含有量は約40~70重量部であることが好ましく、カルシウム粉末の含有量は約50~60重量部であることが好ましい。ゼオライト粉末の含有量が30重量部を下回ると、水素の発生量が低下して生産性が低下する。これは、後述する水素生成反応に寄与するゼオライト粉末が少な過ぎるためだと考えられる。 When the mixed powder composed of zeolite powder and calcium compound powder is 100 parts by weight, the content of zeolite powder is preferably about 40 to 70 parts by weight, and the content of calcium powder is about 50 to 60 parts by weight. Is preferred. When the content of the zeolite powder is less than 30 parts by weight, the generation amount of hydrogen is lowered and productivity is lowered. This is thought to be because too little zeolite powder contributes to the hydrogen generation reaction described later.
 カルシウム粉末の含有量が35重量部を下回った場合も、同様に、後述する水素生成反応の速度が低下して、生産性が低下する。また、カルシウム粉末の含有量が62重量部を超えると、発生する水素の中に未反応のカルシウムが含まれることとなり、発生した水素を輸送する配管等の内部にカルシウムが付着し、好ましくない。 Similarly, when the calcium powder content is less than 35 parts by weight, the rate of the hydrogen generation reaction described later is lowered, and the productivity is lowered. On the other hand, when the content of the calcium powder exceeds 62 parts by weight, unreacted calcium is included in the generated hydrogen, and calcium adheres to the inside of a pipe or the like for transporting the generated hydrogen, which is not preferable.
 活性炭粉末は、植物性材料を炭化したものである。具体的には、活性炭粉末は、杉間伐材、やし殻、珪藻土、草花、おが屑、豆腐粕、籾殻、米ぬか等の安価で入手が容易な植物性材料を400~800℃の炉中で炭化して燻炭を生成し、さらにこの燻炭を10-1Pa~10-5Pa程度の真空状態で所定時間加熱処理(温度:400~800℃、時間:60~360分)して生成したものである。 The activated carbon powder is carbonized vegetable material. Specifically, the activated carbon powder is carbonized in a furnace at 400-800 ° C, which is cheap and readily available, such as cedar thinned wood, coconut husk, diatomaceous earth, grass, flowers, sawdust, tofu lees, rice husks, rice bran. As a result, the charcoal was produced, and further, this charcoal was produced by heat treatment for a predetermined time (temperature: 400-800 ° C., time: 60-360 minutes) in a vacuum state of about 10 −1 Pa to 10 −5 Pa. Is.
 活性炭粉末は、炭素化率が90%以上、pHが9.0~11.0である高炭素質を有している。また、活性炭粉末の表面には、約3nm径の多数の微細孔が形成されており、比表面積は1000m/g以上となっている。また、活性炭粉末は様々なフラーレン形状、例えばサッカーボール型、カーボンナノチューブ型、バッキーオニオン型、ホーン型を有している。 The activated carbon powder has a high carbon quality with a carbonization rate of 90% or more and a pH of 9.0 to 11.0. In addition, a large number of fine pores having a diameter of about 3 nm are formed on the surface of the activated carbon powder, and the specific surface area is 1000 m 2 / g or more. The activated carbon powder has various fullerene shapes such as a soccer ball type, a carbon nanotube type, a bucky onion type, and a horn type.
 β鉄シリサイドは、クラーク数が高く、かつ人体に対して毒性がない元素からなるいわゆる環境半導体の一種であり、常温で数ミリHz~数テラHzの帯域の電磁波を放射することが知られている。 β-iron silicide is a kind of so-called environmental semiconductor composed of elements that have a high Clarke number and are not toxic to the human body, and is known to emit electromagnetic waves in the band of several milliHz to several teraHz at room temperature. Yes.
 β鉄シリサイドは、粉末状にして活性炭粉末とともに混合粉末に添加することができる。混合粉末を100重量部とした場合のβ鉄シリサイドおよび活性炭粉末の添加量は、それぞれ0.1重量部以上であればよい。すなわち、混合粉末に微量のβ鉄シリサイドおよび活性炭粉末を添加するだけで、後述する水素生成反応により、大量の水素を長時間に亘って発生させることができる水素発生剤となる。 Β-iron silicide can be powdered and added to the mixed powder together with the activated carbon powder. When the mixed powder is 100 parts by weight, the addition amount of β iron silicide and activated carbon powder may be 0.1 parts by weight or more. That is, it becomes a hydrogen generator capable of generating a large amount of hydrogen over a long period of time by adding a small amount of β-iron silicide and activated carbon powder to the mixed powder by a hydrogen generation reaction described later.
 また、β鉄シリサイドは、フェノール樹脂中に分散させて水素生成反応に供される水を貯留する容器の底に配置したり、スラリー化させて容器の内部に塗布したりすることもできる。このようにしても、β鉄シリサイドは、後述する水素生成反応に寄与することができる。なお、本願の明細書および特許請求の範囲中の用語“浸漬”には、貯留されている水に水素発生剤を投入することだけでなく、水素発生剤を構成するβ鉄シリサイドをあらかじめ塗布等しておいた容器に水を貯留することも含まれるものとする。 Also, β-iron silicide can be dispersed in a phenolic resin and placed at the bottom of a container for storing water to be used for the hydrogen generation reaction, or can be slurried and applied to the inside of the container. Even in this case, β-iron silicide can contribute to the hydrogen generation reaction described later. In addition, the term “immersion” in the specification and claims of this application not only applies a hydrogen generating agent to stored water but also pre-applies β iron silicide constituting the hydrogen generating agent. It shall also include storing water in a previously prepared container.
 カルシウム化合物として水酸化カルシウムを使用した水素発生剤を水に浸漬させると、基本的には、以下に示す既知の水素生成反応が行われ、水素が発生すると考えられる。

  Ca(OH)+2Al+2HO → CaO・Al+3H

 ここで、反応式左辺のAlは、ゼオライト粉末に含まれているアルミニウムである。
When a hydrogen generator using calcium hydroxide as a calcium compound is immersed in water, basically, the following known hydrogen generation reaction is performed, and hydrogen is considered to be generated.

Ca (OH) 2 + 2Al + 2H 2 O → CaO · Al 2 O 3 + 3H 2

Here, Al on the left side of the reaction formula is aluminum contained in the zeolite powder.
 また、上記反応とともに、水が活性炭粉末の微細孔に高速回転しながら吸い込まれ、活性炭粉末の周辺の水が微振動する。そして、この微振動によって刺激されたβ鉄シリサイドからより多くの電磁波が放出され、上記反応が促進される。 Also, along with the above reaction, water is sucked into the fine pores of the activated carbon powder while rotating at high speed, and the water around the activated carbon powder vibrates slightly. And more electromagnetic waves are emitted from the β-iron silicide stimulated by this micro vibration, and the reaction is promoted.
 すなわち、本発明によれば、ゼオライト粉末とカルシウム化合物粉末とからなる混合粉末に活性炭粉末とβ鉄シリサイドとを添加することによって、上記既知の水素生成反応が促進され、短時間で大量の水素を発生させることができ、しかも長期間に亘って水素を発生させ続けることができる。 That is, according to the present invention, by adding activated carbon powder and β-iron silicide to a mixed powder composed of zeolite powder and calcium compound powder, the known hydrogen generation reaction is promoted, and a large amount of hydrogen is generated in a short time. Hydrogen can be generated over a long period of time.
 続いて、本発明に係る水素発生剤(実施例1、2)と比較のために従来の水素発生剤(従来例)とを用いて、水素を発生させた実験結果について説明する。
Figure JPOXMLDOC01-appb-T000001
Subsequently, experimental results of generating hydrogen using the hydrogen generator according to the present invention (Examples 1 and 2) and a conventional hydrogen generator (conventional example) will be described for comparison.
Figure JPOXMLDOC01-appb-T000001
 上表に示すように、実施例1に係る水素発生剤は、ゼオライト粉末48gと水酸化カルシウム粉末50gとからなる混合粉末に、杉間伐材を炭化等して得た比表面積1000m/g以上の活性炭粉末1gとβ鉄シリサイド粉末1gとを添加し、計100gとしたものである。実施例2に係る水素発生剤は、実施例1に係る水素発生剤にさらにマグネシウムシリサイド(MgSi)の粉末1gを添加し、ゼオライト粉末を47gとしたものである。従来例に係る水素発生剤は、β鉄シリサイドを添加せず、ゼオライト粉末を49gとしたものである。また、実験では、ガラス容器に貯留した500mlの水に各水素発生剤を浸漬させ、一定時間毎の水素発生量を流量計で測定した。 As shown in the table above, the hydrogen generating agent according to the first embodiment, the mixed powder consisting of a zeolite powder 48g calcium hydroxide powder 50 g, cedar thinnings carbide or the like to give specific surface area 1000 m 2 / g or more 1 g of activated carbon powder and 1 g of β iron silicide powder were added to make a total of 100 g. The hydrogen generator according to Example 2 is obtained by further adding 1 g of magnesium silicide (MgSi 2 ) powder to the hydrogen generator according to Example 1 to obtain 47 g of zeolite powder. The hydrogen generator according to the conventional example is obtained by adding 49 g of zeolite powder without adding β-iron silicide. Moreover, in experiment, each hydrogen generating agent was immersed in 500 ml of water stored in the glass container, and the amount of hydrogen generation for every fixed time was measured with the flow meter.
 なお、上記水素生成反応が進行すると、水温が上昇し、水の量が減少するが、本実験では水を適宜補充することによって、水温を45~90℃の範囲に維持しつつ、水量が300mlを下回らないようにした。 As the hydrogen generation reaction proceeds, the water temperature rises and the amount of water decreases. In this experiment, the water amount is maintained in the range of 45 to 90 ° C. by appropriately replenishing water, and the water amount is 300 ml. It was made not to fall below.
 上記条件で試験を行った結果を図1および図2に示す。 The results of testing under the above conditions are shown in FIG. 1 and FIG.
 図1(A)および図2(A)に示すように、実施例1(■)および実施例2(△)に係る水素発生剤によれば、実験開始直後から大量の水素を発生させることができる。例えば、30分経過後の水素総発生量は、従来例(*)が180Lであるのに対して、実施例1が1332L、実施例2が1607Lである。 As shown in FIGS. 1 (A) and 2 (A), according to the hydrogen generating agent according to Example 1 (■) and Example 2 (Δ), a large amount of hydrogen can be generated immediately after the start of the experiment. it can. For example, the total amount of hydrogen generated after 30 minutes is 180 L in the conventional example (*), but 1332 L in the first example and 1607 L in the second example.
 また、従来例に係る水素発生剤では、約24時間経過するとほとんど水素が発生しなくなる(特に、図2(B)参照)。これに対して、図1(C)および図2(C)に示すように、実施例1および実施例2に係る水素発生剤によれば、24時間を経過した後も少なくとも5日を経過するまではほぼ一定の量の水素を発生させ続けることができる。 Also, the hydrogen generating agent according to the conventional example hardly generates hydrogen after about 24 hours (particularly, refer to FIG. 2B). On the other hand, as shown in FIG. 1C and FIG. 2C, according to the hydrogen generating agent according to Example 1 and Example 2, at least 5 days pass even after 24 hours. Until then, a substantially constant amount of hydrogen can continue to be generated.
 また、実施例1と実施例2とを比較すると、マグネシウムシリサイドをさらに添加した実施例2の方が実験開始直後約90分間の水素発生量が多かった。これは、マグネシウムシリサイドが上記水素生成反応をさらに促進させたからだと考えられる。なお、マグネシウムシリサイドに替えて、酸化マグネシウム(MgO)を添加した場合でも従来型と比較し水素発生量が増加することが確認できた。 Further, comparing Example 1 and Example 2, Example 2 to which magnesium silicide was further added had a larger amount of hydrogen generation for about 90 minutes immediately after the start of the experiment. This is presumably because magnesium silicide further promoted the hydrogen generation reaction. In addition, it was confirmed that the amount of hydrogen generation increased when magnesium oxide (MgO) was added instead of magnesium silicide as compared with the conventional type.
[水素発生装置]
 次に、図3を参照しながら、本発明に係る水素発生装置の好ましい実施形態について説明する。
[Hydrogen generator]
Next, a preferred embodiment of the hydrogen generator according to the present invention will be described with reference to FIG.
 図3に示すように、本発明に係る水素発生装置1は、ガラス製の容器本体2aおよび当該容器本体2aを密封する蓋2bからなる容器2と、容器2の中に水素発生剤を投入するための投入口3と、発生した水素を容器2の外に取り出すための水素取出口7と、容器2内に水を貯留するための水注入手段6とを備える。この他、水素発生装置1は、容器2に貯留されている水8の温度を測定するための水温測定手段4と、水8の量を測定するための水量測定手段5とを備えている。水温測定手段4および水量測定手段5から出力される信号は、水注入手段6に入力される。 As shown in FIG. 3, the hydrogen generator 1 according to the present invention introduces a hydrogen generating agent into a container 2 composed of a glass container body 2 a and a lid 2 b that seals the container body 2 a. And a water inlet 7 for taking out the generated hydrogen out of the container 2 and a water injection means 6 for storing water in the container 2. In addition, the hydrogen generator 1 includes a water temperature measuring unit 4 for measuring the temperature of the water 8 stored in the container 2 and a water amount measuring unit 5 for measuring the amount of the water 8. Signals output from the water temperature measuring means 4 and the water amount measuring means 5 are input to the water injection means 6.
 この水素発生装置1で水素を発生させる際は、はじめに水注入手段6で容器2内に適当な量の水を貯留する。そして、投入口3の栓を外し、そこから水素発生剤を投入して浸漬させる。発生した水素は、水素取出口7を通って取り出され、ガスタンクに貯蔵される。 When hydrogen is generated by the hydrogen generator 1, an appropriate amount of water is first stored in the container 2 by the water injection means 6. And the stopper of the insertion port 3 is removed, and a hydrogen generating agent is thrown in from there and immersed. The generated hydrogen is taken out through the hydrogen outlet 7 and stored in the gas tank.
 水素が発生している間、水温測定手段4は水8の温度を測定し、水量測定手段5は水8の量を測定する。そして、水温測定手段4および水量測定手段5は、それぞれ測定結果に応じた信号を出力する。水注入手段6は、水量が所定の閾値を下回った旨の信号または水温が所定の閾値を上回った旨の信号が入力されると、容器2内に適当な量の新たな水を補充する。これにより、水温が高くなり過ぎたり、水が減り過ぎたりするのが防止される。 During the generation of hydrogen, the water temperature measuring means 4 measures the temperature of the water 8 and the water amount measuring means 5 measures the amount of the water 8. Then, the water temperature measuring means 4 and the water amount measuring means 5 each output a signal corresponding to the measurement result. When a signal indicating that the amount of water has fallen below a predetermined threshold or a signal indicating that the water temperature has exceeded a predetermined threshold is input, the water injection means 6 replenishes the container 2 with an appropriate amount of new water. Thereby, it is prevented that the water temperature becomes too high or the water becomes too low.
 この水素発生装置1によれば、水素の発生が始まった後の水温および水量の調整が自動化され、手間がかからないので、水素の製造コストを低減することができる。 According to the hydrogen generator 1, since the adjustment of the water temperature and the amount of water after the generation of hydrogen is automated and takes less time, the production cost of hydrogen can be reduced.
 以上、本発明に係る水素発生剤、水素発生方法および水素発生装置の好ましい実施形態について説明してきたが、本発明は上記の構成に限定されるものではない。 The preferred embodiments of the hydrogen generating agent, the hydrogen generating method, and the hydrogen generating apparatus according to the present invention have been described above, but the present invention is not limited to the above configuration.
 例えば、上記水素発生装置では、水温と水量の両方に基づいて水が補充されるようになっているが、いずれか一方にのみ基づいて補充されるようにしてもよい。
 また、天然および人工の各種ゼオライト粉末、水酸化カルシウム以外のカルシウム化合物粉末、杉間伐材以外の植物性材料からなる活性炭粉末を使用した場合も、上記とほぼ同様の水素発生効果を得ることができる。
 また、水素発生剤を浸漬させる水は純水に限定されず、水道水または海水を使用した場合も、上記とほぼ同様の水素発生効果を得ることができる。
For example, in the hydrogen generator described above, water is replenished based on both the water temperature and the amount of water, but may be replenished based on only one of them.
In addition, when using various kinds of natural and artificial zeolite powders, calcium compound powders other than calcium hydroxide, and activated carbon powders made of plant materials other than cedar thinning materials, the same hydrogen generation effect as described above can be obtained. .
Moreover, the water in which the hydrogen generating agent is immersed is not limited to pure water, and even when tap water or seawater is used, the same hydrogen generating effect as described above can be obtained.
1  水素発生装置
2  容器
3  投入口
4  水温測定手段
5  水量測定手段
6  水注入手段
7  水素取出口
8  水
DESCRIPTION OF SYMBOLS 1 Hydrogen generator 2 Container 3 Inlet 4 Water temperature measuring means 5 Water quantity measuring means 6 Water injection means 7 Hydrogen outlet 8 Water

Claims (6)

  1.  水に浸漬されると水素を発生させる水素発生剤であって、
     Al、Siおよびアルカリ金属を少なくとも含むゼオライト粉末と、カルシウム化合物粉末とからなる混合粉末と、
     多数の微細孔を有し、比表面積が1000m/g以上である活性炭粉末と、
     β鉄シリサイドと、
    を含み、前記混合粉末を100重量部とすると、前記活性炭粉末および前記β鉄シリサイドはそれぞれ0.1重量部以上であることを特徴とする水素発生剤。
    A hydrogen generator that generates hydrogen when immersed in water,
    A mixed powder comprising a zeolite powder containing at least Al, Si and an alkali metal, and a calcium compound powder;
    Activated carbon powder having a large number of micropores and having a specific surface area of 1000 m 2 / g or more;
    β iron silicide,
    The activated carbon powder and the β-iron silicide are each 0.1 parts by weight or more when the mixed powder is 100 parts by weight.
  2.  0.1重量部以上のマグネシウム化合物をさらに含むことを特徴とする請求項1に記載の水素発生剤。 The hydrogen generator according to claim 1, further comprising 0.1 parts by weight or more of a magnesium compound.
  3.  前記活性炭粉末は、杉間伐材、やし殻、珪藻土、草花、おが屑、豆腐粕、籾殻および米ぬかから選択された少なくとも1種類の植物性材料を炭化させたものであることを特徴とする請求項1または2に記載の水素発生剤。 The activated carbon powder is obtained by carbonizing at least one plant material selected from cedar thinned wood, coconut shell, diatomaceous earth, flower, sawdust, tofu cake, rice husk and rice bran. The hydrogen generator according to 1 or 2.
  4.  請求項1~3のいずれかに記載の水素発生剤を用いた水素発生方法であって、
     粉末状の前記β鉄シリサイドを、少なくとも前記混合粉末および前記活性炭粉末とともに前記水に投入して浸漬させることを特徴とする水素発生方法。
    A hydrogen generation method using the hydrogen generator according to any one of claims 1 to 3,
    A method for generating hydrogen, characterized in that the powdered β-iron silicide is poured and immersed in the water together with at least the mixed powder and the activated carbon powder.
  5.  請求項1~3のいずれかに記載の水素発生剤を用いた水素発生方法であって、
     内表面に前記β鉄シリサイドをあらかじめ配しておいた容器に前記水を貯留し、貯留された前記水に少なくとも前記混合粉末および前記活性炭粉末を投入して浸漬させることを特徴とする水素発生方法。
    A hydrogen generation method using the hydrogen generator according to any one of claims 1 to 3,
    A method of generating hydrogen, characterized in that the water is stored in a container in which the β-iron silicide is arranged in advance on an inner surface, and at least the mixed powder and the activated carbon powder are poured and immersed in the stored water. .
  6.  請求項4または請求項5に記載の水素発生方法を用いて水素を発生させる水素発生装置であって、
     水を貯留するための容器と、
     少なくとも前記混合粉末および前記活性炭粉末を前記容器内に投入するための投入口と、
     前記容器に貯留されている前記水の温度を測定する水温測定手段と、
     前記容器に貯留されている前記水の量を測定する水量測定手段と、
     前記水温測定手段および/または前記水量測定手段の測定結果に基づいて、前記水を注入する水注入手段と、
     発生した水素を取り出すための水素取出口と、
    を備えたことを特徴とする水素発生装置。
    A hydrogen generation apparatus that generates hydrogen using the hydrogen generation method according to claim 4 or 5,
    A container for storing water;
    An inlet for charging at least the mixed powder and the activated carbon powder into the container;
    Water temperature measuring means for measuring the temperature of the water stored in the container;
    Water amount measuring means for measuring the amount of water stored in the container;
    Water injection means for injecting the water based on the measurement result of the water temperature measurement means and / or the water amount measurement means;
    A hydrogen outlet for taking out the generated hydrogen;
    A hydrogen generator characterized by comprising:
PCT/JP2009/068191 2009-10-22 2009-10-22 Hydrogen generating agent, hydrogen generating method employing said generating agent, and hydrogen generating apparatus WO2011048685A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012140726A1 (en) * 2011-04-12 2012-10-18 日本水素発電株式会社 Hydrogen generating agent, method for generating hydrogen using said generating agent and device for generating hydrogen
WO2019049611A1 (en) * 2017-09-08 2019-03-14 杉山 修 Production method for hydrogen gas
JP2019081170A (en) * 2017-10-30 2019-05-30 友達晶材股▲ふん▼有限公司AUO Crystal Corporation Production method of filter and the filter
WO2020245719A1 (en) 2019-06-05 2020-12-10 Sunergy Silicon powder composition for hydrogen production

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS549189A (en) * 1975-10-27 1979-01-23 Agency Of Ind Science & Technol Method of thermochemical producing hydrogen and oxygne from water
JP2001233601A (en) * 2000-02-22 2001-08-28 Hitachi Zosen Corp Method for producing hydrogen
JP2004269296A (en) * 2003-03-06 2004-09-30 Kurosaki Harima Corp Hydrogen producing method by decomposition of water and reaction medium used for the same
JP2005239488A (en) * 2004-02-26 2005-09-08 Tohoku Techno Arch Co Ltd Thermochemical decomposition method for water
JP2009179526A (en) * 2008-01-31 2009-08-13 Toho Gas Co Ltd Method for reducing metal oxide, method for producing hydrogen, and hydrogen storage device

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS549189A (en) * 1975-10-27 1979-01-23 Agency Of Ind Science & Technol Method of thermochemical producing hydrogen and oxygne from water
JP2001233601A (en) * 2000-02-22 2001-08-28 Hitachi Zosen Corp Method for producing hydrogen
JP2004269296A (en) * 2003-03-06 2004-09-30 Kurosaki Harima Corp Hydrogen producing method by decomposition of water and reaction medium used for the same
JP2005239488A (en) * 2004-02-26 2005-09-08 Tohoku Techno Arch Co Ltd Thermochemical decomposition method for water
JP2009179526A (en) * 2008-01-31 2009-08-13 Toho Gas Co Ltd Method for reducing metal oxide, method for producing hydrogen, and hydrogen storage device

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012140726A1 (en) * 2011-04-12 2012-10-18 日本水素発電株式会社 Hydrogen generating agent, method for generating hydrogen using said generating agent and device for generating hydrogen
WO2019049611A1 (en) * 2017-09-08 2019-03-14 杉山 修 Production method for hydrogen gas
JPWO2019049611A1 (en) * 2017-09-08 2020-11-19 杉山 修 Hydrogen gas manufacturing method
US11465902B2 (en) 2017-09-08 2022-10-11 Osamu Sugiyama Method for producing hydrogen gas
JP2019081170A (en) * 2017-10-30 2019-05-30 友達晶材股▲ふん▼有限公司AUO Crystal Corporation Production method of filter and the filter
WO2020245719A1 (en) 2019-06-05 2020-12-10 Sunergy Silicon powder composition for hydrogen production
FR3096980A1 (en) * 2019-06-05 2020-12-11 Sunergy Composition based on silicon powder for the production of hydrogen

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