JPS6149241B2 - - Google Patents
Info
- Publication number
- JPS6149241B2 JPS6149241B2 JP53035287A JP3528778A JPS6149241B2 JP S6149241 B2 JPS6149241 B2 JP S6149241B2 JP 53035287 A JP53035287 A JP 53035287A JP 3528778 A JP3528778 A JP 3528778A JP S6149241 B2 JPS6149241 B2 JP S6149241B2
- Authority
- JP
- Japan
- Prior art keywords
- water
- hydrogen
- reaction
- reactor
- metal hydride
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/06—Combination of fuel cells with means for production of reactants or for treatment of residues
- H01M8/0606—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
- H01M8/065—Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants by dissolution of metals or alloys; by dehydriding metallic substances
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/36—Hydrogen production from non-carbon containing sources, e.g. by water electrolysis
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Sustainable Development (AREA)
- Sustainable Energy (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Fuel Cell (AREA)
Description
【発明の詳細な説明】
本発明は、金属水素化物と水との反応により発
生する水素量を、水素の消費量に応じて、制御し
得る水素発生装置に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a hydrogen generating device that can control the amount of hydrogen generated by a reaction between a metal hydride and water in accordance with the amount of hydrogen consumed.
この種の水素発生装置は、例えば水素・空気
(または酸素)燃料電池の簡便な燃料源として用
いられるもので、金属水素化物、例えば水素化カ
ルシウム、水素化リチウムなどと、水とを反応さ
せて水素を発生させる仕組となつている。しかる
に、金属水素化物と水との反応速度は極めて早
く、反応装置内部の水素ガス圧が過大圧にまで急
激に上昇するという問題があつた。この問題を解
決する手段として、反応速度を遅くする方法が、
多く採用されていた。例えば、金属水素化物を特
種な形状にする方法または、金属水素化物に水と
反応しない不純物を混合する方法などが既に提案
されている。しかし、これらの方法は、水素を発
生する必要がなくなつて、水の供給が停止されて
も、遅れていた反応が進行して、ガス圧が過上昇
する虞れがあつた。従来、このために、発生装置
の耐圧性を増強するかまたは発生装置に安全弁を
設けて、所定圧力以上の水素を放出して、発生水
素による過圧を防止している。このうち、耐圧性
の増強は発生装置の重量および体積が増加する。
また、水素の放出は原料である水素化物の利用効
率が低下するという欠点があつた。さらに、これ
らの方法は反応速度を遅くする方法であるから、
水素の発生が急に必要なときには、この要求に応
じられないという問題があつた。 This type of hydrogen generator is used, for example, as a simple fuel source for hydrogen/air (or oxygen) fuel cells, and is made by reacting water with a metal hydride, such as calcium hydride or lithium hydride. It is designed to generate hydrogen. However, the reaction rate between the metal hydride and water is extremely fast, and there is a problem in that the hydrogen gas pressure inside the reactor rapidly rises to an excessive pressure. One way to solve this problem is to slow down the reaction rate.
It was widely adopted. For example, methods have already been proposed such as forming metal hydrides into special shapes or mixing metal hydrides with impurities that do not react with water. However, in these methods, even when there is no longer a need to generate hydrogen and the supply of water is stopped, there is a risk that the delayed reaction will proceed and the gas pressure will rise excessively. Conventionally, for this purpose, the pressure resistance of the generator is increased or a safety valve is provided in the generator to release hydrogen at a predetermined pressure or higher to prevent overpressure caused by the generated hydrogen. Among these, increasing pressure resistance increases the weight and volume of the generator.
Furthermore, the release of hydrogen has the disadvantage that the utilization efficiency of the hydride, which is a raw material, decreases. Furthermore, since these methods slow down the reaction rate,
There was a problem in that when there was a sudden need to generate hydrogen, this request could not be met.
本発明は、上述の点に鑑み、従来技術の欠点を
除き水素の消費量の変化に応じて、水素の発生量
を速やかにしかも連続的に制御することができ、
過圧の発生の虞れを防止しつつ、金属水素化物の
利用効率の向上を図ることのできる水素発生装置
を提供することを目的とする。 In view of the above-mentioned points, the present invention eliminates the drawbacks of the prior art and allows the amount of hydrogen generated to be quickly and continuously controlled in accordance with changes in the amount of hydrogen consumed.
It is an object of the present invention to provide a hydrogen generator that can improve the efficiency of using metal hydrides while preventing the risk of overpressure.
この目的を達成するために、先づ考えられるこ
とは、金属水素化物への供給水量を、発生水素量
に応じて制御することであるが、反応速度を考慮
に入れた場合には、かなり複雑な制御が要求さ
れ、簡便な燃料源としての要求に合致しない。こ
のために本発明者等は水のかわりに水蒸気を用い
ることを考え、種々実験したところ、比較的少な
い水量で広範囲にわたる反応が得られることが判
明した。水素発生量は供給される水量に比例する
から水蒸気の形で供給すれば比較的少ない水素発
生量を短時間で得ることができることになる。 To achieve this objective, the first thing to consider is to control the amount of water supplied to the metal hydride according to the amount of hydrogen generated, but this is quite complicated when the reaction rate is taken into account. Therefore, it does not meet the requirements as a simple fuel source. For this reason, the inventors of the present invention considered using steam instead of water, and after conducting various experiments, it was found that a wide range of reactions could be obtained with a relatively small amount of water. Since the amount of hydrogen generated is proportional to the amount of water supplied, if it is supplied in the form of steam, a relatively small amount of hydrogen can be generated in a short time.
ところで、水蒸気を発生させる装置を別個に設
けたのでは、やはり簡便な燃料源としての要求に
反する。そこで、本発明者等はさらに検討を進め
た結果、水と金属水素化物との反応の際に生ずる
反応熱に着目し、この反応熱にて供給水を水蒸気
化すれば、簡便な装置としての要求を満しつつ、
上述の目的を達成することができるという結論に
達した。 By the way, providing a separate device for generating water vapor would go against the requirement of a simple fuel source. Therefore, as a result of further investigation, the present inventors focused on the reaction heat generated during the reaction between water and metal hydride, and found that if the supplied water was vaporized using this reaction heat, it could be used as a simple device. While meeting the requirements
It has been concluded that the above objectives can be achieved.
従つて、前述の目的は本発明によれば、金属水
素化物を収容する反応器と、この反応器に設けら
れて、前記金属水素化物に水を供給する水供給管
とを備え、前記供給水が前記金属水素化物と反応
して水素を発生する際に生ずる反応熱により、前
記供給水を前記水供給管内で水蒸気化せしめるこ
とにより達成される。 Accordingly, the above-mentioned object, according to the invention, comprises a reactor containing a metal hydride and a water supply pipe provided in the reactor for supplying water to the metal hydride, the supply water being This is achieved by vaporizing the feed water in the water supply pipe using the heat of reaction generated when the metal hydride reacts with the metal hydride to generate hydrogen.
次に、本発明の実施例を図面に基づき、詳細に
説明する。 Next, embodiments of the present invention will be described in detail based on the drawings.
第1図は本発明の一実施例の概略構成図を示
す。図において水タンク1は供給水を収容し、ガ
ス圧、バネ圧またはその他の方法により加圧し
て、水量調節バルブ3および逆止弁4を経て、反
応器5へ供給水を供給する。反応器5内には水供
給管6が設けられ、金属水素化物7が収容されて
いる。11は水供給管6の末端部10に設けられ
た吹出口である。また、8は発生水素流出弁、9
は安全弁である。 FIG. 1 shows a schematic configuration diagram of an embodiment of the present invention. In the figure, a water tank 1 contains feed water, pressurizes it by gas pressure, spring pressure or other methods, and supplies the feed water to a reactor 5 through a water flow control valve 3 and a check valve 4. A water supply pipe 6 is provided in the reactor 5, and a metal hydride 7 is accommodated therein. Reference numeral 11 denotes an outlet provided at the end portion 10 of the water supply pipe 6. In addition, 8 is a generated hydrogen outflow valve, 9
is a safety valve.
次に、上述の構成によりその機能を説明する。
最初、水タンク1から供給された供給水は、金属
水素化物7内を上部から下部方向へ挿入された波
形状の水供給管6を経由して、末端部10の吹出
口11より流出する。この供給水は近接する金属
水素化物、例えば水素化カルシウム(CaH2)7と
反応して、水素および反応熱を発生する。この反
応式を第(1)式に示す。 Next, the functions of the above-described configuration will be explained.
Initially, the supply water supplied from the water tank 1 flows out from the outlet 11 of the end portion 10 via the corrugated water supply pipe 6 inserted from the top to the bottom inside the metal hydride 7. This feed water reacts with an adjacent metal hydride, such as calcium hydride (CaH 2 ), to generate hydrogen and the heat of reaction. This reaction formula is shown in equation (1).
CaH2+2H2O→
Ca(OH)2+2H2+49kcal/mole ……(1)
この反応熱により、反応器5内の温度が上昇す
る。本発明者等の実測によれば、熱交換率を高め
るために、水供給管6の内径が比較的小さく選定
されたとき、末端部10内の供給水の温度は、約
300℃程度に達することが確認された。従つて、
供給水は水供給管6内で完全に水蒸気化して、吹
出口11から流出する。この水蒸気化した供給水
は、液体である供給水より流動性がよく、反応器
5内の広範囲に拡散し、吹出口11の付近に限ら
ず、水では到達し難い個所にある水素化カルシウ
ム7とも反応して、水素を発生する。このように
反応器5内で全面的に反応が発生し得るから、吹
出口11付近の水素化カルシウム7が反応を終え
て、もはや水素の発生に寄与しなくなつたとして
も、その影響は少ない。すなわち、水蒸気化した
供給水量を制御することにより、水素発生量の増
減が短時間で得られるから、この水素発生反応の
遅れが減少し、反応器5内の圧力変動が少なくな
る。 CaH 2 +2H 2 O → Ca(OH) 2 +2H 2 +49kcal/mole...(1) The temperature inside the reactor 5 rises due to this reaction heat. According to actual measurements by the present inventors, when the inner diameter of the water supply pipe 6 is selected to be relatively small in order to increase the heat exchange rate, the temperature of the supply water in the end portion 10 is approximately
It was confirmed that the temperature reached around 300℃. Therefore,
The supplied water is completely vaporized within the water supply pipe 6 and flows out from the outlet 11. This vaporized feed water has better fluidity than liquid feed water, and spreads over a wide area in the reactor 5, and is not limited to the vicinity of the outlet 11, but is located in calcium hydride 7, which is difficult to reach with water. It also reacts with hydrogen to generate hydrogen. In this way, the reaction can occur throughout the reactor 5, so even if the calcium hydride 7 near the outlet 11 finishes its reaction and no longer contributes to the generation of hydrogen, the effect is small. . That is, by controlling the amount of water vaporized to be supplied, the amount of hydrogen generated can be increased or decreased in a short time, so the delay in the hydrogen generation reaction is reduced, and the pressure fluctuation in the reactor 5 is reduced.
なお、水供給管6の末端部10が、反応器5の
底部にぴつたりと付けられた場合、未端部10の
付近の水素化カルシウム7から反応が終つて、水
素の発生に寄与しなくなると、次の使用時に水素
発生反応は末端部10から遠ざかつた反応器5の
上層部にまで水が到達してからはじめて行われる
から、反応速度が遅くなるという問題があつた。
このために、末端部10を反応器5の底部からD
だけ高い位置に設けると、反応器5内の反応が、
まず水の状態で供給される供給水により末端部の
下層部で行なわれ、次いでこの反応により発生す
る反応熱によつて生じる水蒸気により、末端部1
0の上層部に反応が移行するため、末端部10の
下層部には未反応の水素化カルシウムが残ること
になる。従つて次の使用時に供給水が再び水の状
態で供給された際にも、下層部での反応が再び行
なわれるので、反応速度の低下がなくなる。上層
部に存在する水素化カルシウム7の反応が完了す
る際に、下層部に存在する水素化カルシウム7の
反応がちようど完了するように距離Dを選べば、
水素化カルシウム7の利用効率の向上を図ること
ができる。 In addition, if the end part 10 of the water supply pipe 6 is tightly attached to the bottom of the reactor 5, the reaction will be completed from the calcium hydride 7 near the end part 10, and it will no longer contribute to the generation of hydrogen. However, when the reactor is next used, the hydrogen generation reaction is carried out only after the water reaches the upper layer of the reactor 5, which is far from the end portion 10, resulting in a slow reaction rate.
For this purpose, the end part 10 is inserted from the bottom of the reactor 5 into the D
If the reactor 5 is installed at a higher position, the reaction inside the reactor 5 will be
First, water supplied in the form of water causes the reaction to occur in the lower layer of the end part, and then water vapor generated by the reaction heat generated by this reaction causes the reaction to occur in the lower part of the end part.
Since the reaction moves to the upper layer of 0, unreacted calcium hydride remains in the lower layer of the end portion 10. Therefore, even when the feed water is supplied in the form of water again during the next use, the reaction in the lower layer is carried out again, so there is no reduction in the reaction rate. If the distance D is selected so that the reaction of the calcium hydride 7 present in the lower layer is likely to be completed when the reaction of the calcium hydride 7 present in the upper layer is completed,
The utilization efficiency of calcium hydride 7 can be improved.
次に、第2図は第1図における発生水素供給量
変化による反応器内圧変化状態図を示す。図にお
いて線Aは発生水素供給量変化、線Bは発生水素
の供給量変化により生ずる反応器5内の圧力変化
である。水素供給量が時間的に、例えば0.5/mi
nないし1.5/minの変化を生じた際、反応器5
内の内圧変化が1.5Kg/cm2Gないし3.0Kg/cm2Gの範
囲内で安定している。すなわち、供給水が水蒸気
化して供給されるために、水素化カルシウム7と
の反応遅れが減少して、反応速度が向上したこと
により、水素の消費量に応じて、水素の発生量が
速かに追従して増減し得るようになつたためであ
る。 Next, FIG. 2 shows a state diagram of changes in the internal pressure of the reactor due to changes in the amount of hydrogen supplied in FIG. 1. In the figure, line A shows the change in the amount of hydrogen supplied, and line B shows the change in pressure inside the reactor 5 caused by the change in the amount of hydrogen supplied. If the hydrogen supply amount is temporally, e.g. 0.5/mi
When a change of n to 1.5/min occurs, reactor 5
The internal pressure change within the chamber is stable within the range of 1.5Kg/cm 2 G to 3.0Kg/cm 2 G. In other words, since the feed water is supplied in the form of steam, the reaction delay with calcium hydride 7 is reduced and the reaction rate is improved, so that the amount of hydrogen generated is faster depending on the amount of hydrogen consumed. This is because it has become possible to increase and decrease following the.
次に、第3図は本発明の他の実施例の概略構成
図を示す。図において反応器5内に上部から下部
方向へ挿入された水供給管14には、複数個の吸
熱フイン15が設けられている。この吸熱フイン
15の大きさおよび数量は、反応熱が水供給管1
4内の供給水に吸収されて、供給水が完全に水蒸
気化されるように選定される。 Next, FIG. 3 shows a schematic configuration diagram of another embodiment of the present invention. In the figure, a water supply pipe 14 inserted into the reactor 5 from the top to the bottom is provided with a plurality of heat-absorbing fins 15. The size and number of the heat-absorbing fins 15 are such that the heat of reaction is absorbed by the water supply pipe 1.
4, so that the feed water is completely vaporized.
次に、第4図は本発明のさらに他の実施例の概
略構成図を示す。図において反応器5の外周に上
部から下部方向に向かつて、水供給管16がコイ
ル状に巻回され、末端部10が反応器5内へ挿入
され、吹出口11から水蒸気化した供給水が流出
するように構成されている。このコイル状の巻回
数は、反応器5内の反応熱が水供給管13内の供
給水に吸収されて、供給水は完全に水蒸気化され
るように選定される。 Next, FIG. 4 shows a schematic configuration diagram of still another embodiment of the present invention. In the figure, a water supply pipe 16 is wound around the outer periphery of the reactor 5 in a coil shape from the top to the bottom, the end part 10 is inserted into the reactor 5, and the water vaporized water is supplied from the outlet 11. It is configured to flow out. The number of turns of this coil is selected so that the reaction heat in the reactor 5 is absorbed by the feed water in the water supply pipe 13, and the feed water is completely vaporized.
なお、本実施例では、水供給管16は反応器5
の外周にコイル状に巻回されるが、反応器5の内
周にコイル状に巻回することも可能である。 In this embodiment, the water supply pipe 16 is connected to the reactor 5.
Although it is wound in a coil shape around the outer circumference of the reactor 5, it is also possible to wind it in a coil shape around the inner circumference of the reactor 5.
以上に説明するように本発明によれば、水のか
わりに水蒸気を用いることにより、比較的少ない
水量で広範囲に亘る金属水素化物との水素発生反
応が得られ、水素の消費量の変化に応じて、水素
の発生量を速やかにしかも連続的に制御すること
が可能となり、過圧発生の虞れが防止されつつ、
かつ金属水素化物は有効に水蒸気と反応して、金
属水素化物の利用効率の向上が図られる。しか
も、反応に用いられる水蒸気は特別な水蒸気発生
装置を別個に設けることなく、供給水と金属水素
化物との反応の際に発生する反応熱により、水供
給管内で水蒸気化しているのでその構成が簡便で
あるという効果を奏する。 As explained above, according to the present invention, by using steam instead of water, a hydrogen generating reaction with a wide range of metal hydrides can be obtained with a relatively small amount of water, and the hydrogen generation reaction can be performed in response to changes in the amount of hydrogen consumed. This makes it possible to quickly and continuously control the amount of hydrogen generated, while preventing the risk of overpressure.
In addition, the metal hydride reacts effectively with water vapor, and the utilization efficiency of the metal hydride is improved. Furthermore, the water vapor used in the reaction is vaporized in the water supply pipe by the reaction heat generated during the reaction between the feed water and the metal hydride, without the need for a separate special steam generator. It has the effect of being simple.
なお、本実施例では燃料電池に付属される水素
発生装置を例にとつたが、本発明はかかる用途の
みでなく、屋外などで簡単に水素を入手する手段
として有効である。 In this embodiment, a hydrogen generator attached to a fuel cell is used as an example, but the present invention is effective not only for such applications but also as a means for easily obtaining hydrogen outdoors.
第1図は本発明の一実施例の概略構成図、第2
図は第1図における発生水素供給量変化に対する
反応器内圧変化状態図、第3図は本発明の他の実
施例の概略構成図、第4図は本発明のさらに他の
実施例の概略構成図である。
3;水量調節バルブ、4;逆止弁、5;反応
器、6;水供給管、7;金属水素化物、8;発生
水素供給弁、9;安全弁、10;末端部、11;
吹出口、13,14,16;水供給管、15;吸
熱フイン。
FIG. 1 is a schematic configuration diagram of an embodiment of the present invention, and FIG.
The figure is a state diagram of changes in reactor internal pressure with respect to changes in the amount of hydrogen supplied in Figure 1, Figure 3 is a schematic configuration diagram of another embodiment of the present invention, and Figure 4 is a schematic configuration diagram of still another embodiment of the present invention. It is a diagram. 3; Water flow control valve, 4; Check valve, 5; Reactor, 6; Water supply pipe, 7; Metal hydride, 8; Generated hydrogen supply valve, 9; Safety valve, 10; End part, 11;
Air outlet, 13, 14, 16; water supply pipe, 15; heat absorption fin.
Claims (1)
器の上層部にある当該金属水素化物と伝熱的にに
設けられ、前記反応器の下層部にある金属水素化
物に水を供給する水供給管とを備え、前記供給水
が前記金属水素化物と反応して水素を発生する際
に生ずる反応熱により、前記供給水を前記水供給
管内で水蒸気化せしめることを特徴とする水素発
生装置。1. A reactor containing a metal hydride, and a water supply that is thermally connected to the metal hydride in the upper part of the reactor and supplies water to the metal hydride in the lower part of the reactor. A hydrogen generating device comprising: a hydrogen generating apparatus, wherein the supplied water is vaporized in the water supply pipe by reaction heat generated when the supplied water reacts with the metal hydride to generate hydrogen.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3528778A JPS54127891A (en) | 1978-03-29 | 1978-03-29 | Hydrogen generator |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3528778A JPS54127891A (en) | 1978-03-29 | 1978-03-29 | Hydrogen generator |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54127891A JPS54127891A (en) | 1979-10-04 |
| JPS6149241B2 true JPS6149241B2 (en) | 1986-10-28 |
Family
ID=12437548
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3528778A Granted JPS54127891A (en) | 1978-03-29 | 1978-03-29 | Hydrogen generator |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS54127891A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014158091A1 (en) * | 2013-03-25 | 2014-10-02 | Horizon Fuel Cell Technologies Pte. Ltd. | Method and generator for hydrogen production |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4843845B2 (en) | 2000-07-03 | 2011-12-21 | トヨタ自動車株式会社 | Fuel cell system and control method thereof |
| WO2004075375A2 (en) * | 2003-02-19 | 2004-09-02 | Honeywell International Inc. | Electrical power generator |
| US7179443B2 (en) | 2003-02-26 | 2007-02-20 | Daimlerchrysler Corporation | Powder metal hydride hydrogen generator |
| FR2893606B1 (en) * | 2005-11-24 | 2008-04-25 | Commissariat Energie Atomique | HYDROGEN GENERATOR AND FUEL CELL IMPLEMENTING SUCH A GENERATOR |
| JP4868352B2 (en) * | 2005-12-27 | 2012-02-01 | セイコーインスツル株式会社 | Hydrogen generation facility and fuel cell system |
| CN102137810A (en) * | 2008-09-02 | 2011-07-27 | 日立麦克赛尔株式会社 | Hydrogen generation device and fuel cell system equipped with same |
| WO2010084790A1 (en) * | 2009-01-20 | 2010-07-29 | Ishikawa Yasuo | Catalyst for hydrogen generation, method for generating hydrogen, and hydrogen generator |
| US9376317B2 (en) | 2010-01-06 | 2016-06-28 | Yasuo Ishikawa | Method of generating hydrogen |
| JP5365942B2 (en) * | 2011-10-12 | 2013-12-11 | セイコーインスツル株式会社 | Hydrogen generation facility and fuel cell system |
-
1978
- 1978-03-29 JP JP3528778A patent/JPS54127891A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2014158091A1 (en) * | 2013-03-25 | 2014-10-02 | Horizon Fuel Cell Technologies Pte. Ltd. | Method and generator for hydrogen production |
| US10322932B2 (en) | 2013-03-25 | 2019-06-18 | Hes Energy Systems Pte. Ltd. | Method and generator for hydrogen production |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54127891A (en) | 1979-10-04 |
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