JPS6318306B2 - - Google Patents
Info
- Publication number
- JPS6318306B2 JPS6318306B2 JP55152045A JP15204580A JPS6318306B2 JP S6318306 B2 JPS6318306 B2 JP S6318306B2 JP 55152045 A JP55152045 A JP 55152045A JP 15204580 A JP15204580 A JP 15204580A JP S6318306 B2 JPS6318306 B2 JP S6318306B2
- Authority
- JP
- Japan
- Prior art keywords
- gas
- cell
- cooling section
- fuel cell
- fuel
- 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
Links
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
- H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
- H01M8/04007—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids related to heat exchange
- H01M8/04014—Heat exchange using gaseous fluids; Heat exchange by combustion of reactants
-
- 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
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Life Sciences & Earth Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Sustainable Development (AREA)
- Sustainable Energy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Fuel Cell (AREA)
Description
【発明の詳細な説明】
本発明は燃料と酸化剤を電気化学的に反応させ
て電力を発生させる燃料電池に係り、構造が簡略
で好適な温度分布が得られる燃料電池発電装置に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fuel cell that generates electric power by electrochemically reacting a fuel and an oxidizing agent, and relates to a fuel cell power generation device that has a simple structure and provides a suitable temperature distribution.
燃料と酸化剤を電気化学的に反応させて電力を
発生させる装置として燃料電池が知られている。
燃料電池の基本的な構成を第1図に示す。電解質
1をはさんでカソード(酸化剤極)2とアノード
(燃料極)3が向い合わせにして並らべられ、カ
ソード2の電解質とは反対側の面に酸素を含む空
気が供給され、一方アノード3の電解質と反対側
の面には燃料である水素ガスが供給される。 A fuel cell is known as a device that generates electric power by electrochemically reacting a fuel and an oxidizing agent.
The basic configuration of a fuel cell is shown in Figure 1. A cathode (oxidizer electrode) 2 and an anode (fuel electrode) 3 are arranged facing each other with an electrolyte 1 in between, and air containing oxygen is supplied to the surface of the cathode 2 opposite to the electrolyte, while Hydrogen gas, which is a fuel, is supplied to the surface of the anode 3 opposite to the electrolyte.
アノード3もカソード2も導電性材料で作られ
た多孔質体であり、これらの内部に電解質と燃料
ガスが接する界面ができ、この界面で反応が進行
する。 Both the anode 3 and the cathode 2 are porous bodies made of conductive materials, and there is an interface between the electrolyte and the fuel gas inside them, and the reaction proceeds at this interface.
アノード3では水素ガスが水素イオンになる。
電子は外部の負荷4を通つてカソード2に流れ、
電解質中を通つて来た水素イオンおよび空気中の
酸素と結合して水となる。 At the anode 3, hydrogen gas becomes hydrogen ions.
Electrons flow to the cathode 2 through an external load 4,
It combines with hydrogen ions that have passed through the electrolyte and oxygen in the air to form water.
アノード H2→2H++2e- (1)
カソード 2H++1/2O2+2e-→H2O (2)
H2+1/2O2→H2O (3)
結局、燃料の水素と空気中の酸素が水となる反
応である。Anode H 2 →2H + +2e - (1) Cathode 2H + +1/2O 2 +2e - →H 2 O (2) H 2 +1/2O 2 →H 2 O (3) In the end, hydrogen in the fuel and oxygen in the air This is a reaction in which water becomes water.
燃料電池内に進行するこの反応は発熱反応であ
り、電池内を所定の温度に保つには反応熱を定常
的に除去する必要性がある。第2図は電解質とし
て溶融炭酸塩を使用する、通常第2世代燃料電池
と呼ばれる溶融炭酸塩電解質燃料電池(以下
MOFと略称する)を例とした、電池の温度と電
池の出力の間の関係を示したものである。電池に
は下限温度T1がありこの温度以下では電解質の
物性のため急激に出力が低下する。また主として
電池構成部材の使用限界条件から定まる上限温度
T2がある。従つて電池から良好な性能を得るた
めには比較的狭い温度範囲ΔTの中に電池温度を
制御する必要がある。MOFの場合、大きくても
ΔTは100℃以下程度とされている。 This reaction that progresses inside the fuel cell is an exothermic reaction, and in order to maintain the inside of the cell at a predetermined temperature, it is necessary to constantly remove the reaction heat. Figure 2 shows a molten carbonate electrolyte fuel cell (hereinafter referred to as a molten carbonate electrolyte fuel cell, commonly referred to as a second generation fuel cell) that uses molten carbonate as the electrolyte.
This figure shows the relationship between battery temperature and battery output using a MOF (abbreviated as MOF) as an example. Batteries have a lower temperature limit T1 , and below this temperature the output drops rapidly due to the physical properties of the electrolyte. Also, the upper limit temperature is determined mainly by the usage limit conditions of battery components.
There are T2 . Therefore, in order to obtain good performance from the battery, it is necessary to control the battery temperature within a relatively narrow temperature range ΔT. In the case of MOF, ΔT is said to be about 100°C or less at most.
このように、電池内で発生する反応熱を除去し
所定の温度範囲に保持する必要があるため、従来
から諸種の冷却方法が提案されている。 As described above, it is necessary to remove the reaction heat generated within the battery and maintain it within a predetermined temperature range, so various cooling methods have been proposed.
第3図はDIGAS冷却方式と称されている従来
の冷却方式の構成を示したものである。カソー
ド、電解質およびアノードからなる単位電池(セ
ル)5を積層して群電池(スタツク)6が構成さ
れる。スタツク内には冷却部7が設けられてい
る。外部より導入された空気8は熱交換器9を通
つて冷却された再循環ガス10と合流した後、酸
化剤ガス11として入口マニホールド12に入
り、セル5および冷却器7に供給される。セルお
よび冷却部を通つたガスは出口マニホールド13
に集められた後、一部は熱交換器9を通つて再循
環され、残りは廃ガス14として外部に排気され
る。 FIG. 3 shows the configuration of a conventional cooling system called the DIGAS cooling system. A group battery (stack) 6 is constructed by stacking unit batteries (cells) 5 each consisting of a cathode, an electrolyte, and an anode. A cooling section 7 is provided within the stack. Air 8 introduced from the outside passes through a heat exchanger 9 and joins the cooled recirculating gas 10, then enters the inlet manifold 12 as an oxidizing gas 11 and is supplied to the cell 5 and the cooler 7. The gas passing through the cell and the cooling section exits to the outlet manifold 13.
After being collected, a portion is recycled through the heat exchanger 9 and the rest is exhausted to the outside as waste gas 14.
このように構成された従来の冷却方式は次のよ
うな欠点を有していた。 The conventional cooling system configured as described above had the following drawbacks.
第4図は酸化剤ガスのうち冷却部を通過する総
流量のセルを通過する総流量に対する比kとセル
の流れ方向の温度差ΔTCELLの間の関係を示した
もので、パラメータとして冷却部入口温度Tiを
とつている。 Figure 4 shows the relationship between the ratio k of the total flow rate of the oxidant gas passing through the cooling section to the total flow rate passing through the cell, and the temperature difference ΔT CELL in the flow direction of the cell. The inlet temperature is Ti.
第3図の従来方式の場合、酸化剤ガス11がセ
ル5と冷却部7に同時に供給されるため、冷却部
入口ガス温度Tiはセル入口温度と同一であり、
第2図で示したように電池から良好な性能を得る
ためにはこの冷却部入口ガス温度Tiを電池下限
温度T1より大巾に下げることは出来ずT1と同程
度、例えば600℃にせざるを得ない。 In the case of the conventional method shown in FIG. 3, the oxidizing gas 11 is supplied to the cell 5 and the cooling section 7 at the same time, so the cooling section inlet gas temperature Ti is the same as the cell inlet temperature.
As shown in Figure 2, in order to obtain good performance from the battery, the gas temperature Ti at the inlet of the cooling section cannot be lowered much lower than the battery minimum temperature T 1 , and must be at the same level as T 1 , for example 600°C. I have no choice but to.
この場合、セルの温度差ΔTCELLを所定の温度
差ΔT以内、例えば100℃以内にするためには第
4図に示すように冷却部流量をセル流量の15倍程
度も流す必要がある。 In this case, in order to keep the cell temperature difference ΔT CELL within a predetermined temperature difference ΔT, for example within 100° C., the cooling section flow rate must be approximately 15 times the cell flow rate, as shown in FIG.
このことが従来提案された冷却方式の大きな欠
点である。即ち、電池から良好な性能を得るため
には、セルで必要な酸化剤流量の15倍程度の酸化
剤ガスを冷却部に流す必要があり、このため冷却
部寸法が大きくなりまた循環に必要なコンプレツ
サー、熱交換器等の補機類の容量が大きなものと
なつて実用に供しにくい欠点を有していた。 This is a major drawback of conventionally proposed cooling methods. In other words, in order to obtain good performance from the battery, it is necessary to flow approximately 15 times as much oxidant gas into the cooling section as the oxidant flow rate required by the cell, which increases the size of the cooling section and reduces the amount of oxidant gas required for circulation. The capacity of auxiliary equipment such as compressors and heat exchangers was large, making it difficult to put it to practical use.
本発明の目的は上記した従来技術の欠点をなく
し、構造が簡略で好適な温度分布が得られるよう
にした燃料電池発電装置を提供するにある。 SUMMARY OF THE INVENTION An object of the present invention is to eliminate the drawbacks of the prior art described above, and to provide a fuel cell power generation device that has a simple structure and can provide a suitable temperature distribution.
このため、本発明では燃料と酸化剤を電気化学
的に反応させて電力を発生させる燃料電池におい
て、燃料および酸化剤のいずれか一方あるいは両
方を、一旦電池の冷却部分を通過させた後に、そ
れぞれ陰極および陽極に導入するようにしたもの
である。 For this reason, in the present invention, in a fuel cell that generates electric power by electrochemically reacting a fuel and an oxidizer, either one or both of the fuel and the oxidizer is passed through the cooling section of the cell, and then each It is designed to be introduced into the cathode and anode.
以下に実施例に基づいて本発明を説明する。 The present invention will be explained below based on Examples.
第5図は本発明を適用した燃料電池発電装置の
構成例を示したものである。酸化剤ガス11Aは
冷却ガスマニホールド15を通つて冷却部7Aに
導入される。冷却部を通過したガス16はセル入
口マニホールド17から各セル5Aに供給され、
セルを通過後、出口ガスマニホールド18に集め
られ廃ガス14Aとして排気される。 FIG. 5 shows an example of the configuration of a fuel cell power generation device to which the present invention is applied. The oxidant gas 11A is introduced into the cooling section 7A through the cooling gas manifold 15. The gas 16 that has passed through the cooling section is supplied to each cell 5A from the cell inlet manifold 17,
After passing through the cell, it is collected in the outlet gas manifold 18 and exhausted as waste gas 14A.
このように構成した燃料電池発電装置では次の
ような効果が発揮される。即ち、第5図に示した
ように酸化剤ガスは一旦冷却部7Aを通過した後
セル5Aに導入されるため、冷却部入口温度Ti
を電池の下限温度T1程度にする必要がなく大巾
に下げることが出来、例えば400℃程度とするこ
とが可能となる。この時に必要な冷却部の酸化剤
ガス流量は第4図に示すようにセル流量と同量程
度でよいことがわかる。 The fuel cell power generation device configured in this manner exhibits the following effects. That is, as shown in FIG. 5, since the oxidant gas is introduced into the cell 5A after passing through the cooling section 7A, the cooling section inlet temperature Ti
It is not necessary to lower the battery's lower limit temperature T to about 1 , and it can be lowered to a large extent, for example, to about 400°C. It can be seen that the required flow rate of the oxidant gas in the cooling section at this time may be approximately the same as the cell flow rate, as shown in FIG.
このように本発明を適用した燃料電池発電装置
においては、冷却部ガス流量を従来の1/15程度で
セル流量と同量にすることが出来るため、従来例
に比べ冷却部寸法を大巾に小さくすることが可能
となり、また循環に必要なコンプレツサーが不要
になる等、大巾に簡略な構成とすることが可能と
なる。 In this way, in the fuel cell power generation device to which the present invention is applied, the cooling section gas flow rate can be made equal to the cell flow rate at about 1/15 of the conventional one, so the cooling section dimensions can be made much wider than in the conventional example. It becomes possible to make it smaller, and it becomes possible to have a significantly simpler configuration, such as eliminating the need for a compressor required for circulation.
以上の説明では溶融炭酸塩電解質燃料電池の場
合を例にとつたが、本発明の適用がこの型式に限
定されるものでないことは勿論である。 Although the above description has taken the case of a molten carbonate electrolyte fuel cell as an example, it goes without saying that the application of the present invention is not limited to this type.
また、以上の説明では冷却用ガスとして酸化剤
ガスを例にとつたが、燃料ガスを冷却用ガスとし
て用いてもよく、また両者を共に冷却用ガスとし
て用いることも可能である。 Furthermore, in the above description, the oxidant gas was used as an example of the cooling gas, but the fuel gas may be used as the cooling gas, or both may be used as the cooling gas.
また、以上の説明では冷却部をセル数個毎に設
けた場合を例にとつたが、冷却部を設ける箇所は
限定されるものではない。 Further, in the above description, an example is given in which a cooling section is provided for every few cells, but the location where the cooling section is provided is not limited.
第1図は燃料電池の原理を示す略図、第2図は
燃料電池出力と電池温度の関係を示す線図、第3
図は燃料電池発電装置の従来の構成例を示す略
図、第4図は冷却部流量のセル流量に対する比と
セル温度差の関係を示す線図、第5図は本発明を
適用した燃料電池発電装置の構成例を示す略図で
ある。
5,5A……セル、7,7A……冷却部、6,
6A……スタツク、11,11A……酸化剤ガ
ス。
Figure 1 is a schematic diagram showing the principle of a fuel cell, Figure 2 is a diagram showing the relationship between fuel cell output and cell temperature, and Figure 3 is a diagram showing the relationship between fuel cell output and cell temperature.
The figure is a schematic diagram showing an example of a conventional configuration of a fuel cell power generation device, FIG. 4 is a diagram showing the relationship between the ratio of the cooling section flow rate to the cell flow rate and the cell temperature difference, and FIG. 5 is a fuel cell power generation system to which the present invention is applied. It is a schematic diagram showing an example of the configuration of the device. 5,5A...Cell, 7,7A...Cooling part, 6,
6A...Stack, 11,11A...Oxidizer gas.
Claims (1)
位電池を積層した群電池、該群電池内の積層単位
電池間に設けられた冷却部、該冷却部に燃料ガス
および酸化剤ガスのいずれか一方あるいは両方を
導入するガス導入手段、該冷却部を通過したガス
を前記単位電池に供給するガス供給手段を備えた
ことを特徴とする燃料電池発電装置。1 A group battery in which unit cells consisting of a cathode, an electrolyte, and an anode are stacked, a cooling section provided between the stacked unit cells in the group battery, and either or both of a fuel gas and an oxidizing gas introduced into the cooling section. 1. A fuel cell power generation device comprising: a gas introduction means for supplying gas to the unit cells; and a gas supply means for supplying the gas that has passed through the cooling section to the unit cells.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55152045A JPS5776766A (en) | 1980-10-31 | 1980-10-31 | Fuel cell powder generator |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55152045A JPS5776766A (en) | 1980-10-31 | 1980-10-31 | Fuel cell powder generator |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5776766A JPS5776766A (en) | 1982-05-13 |
| JPS6318306B2 true JPS6318306B2 (en) | 1988-04-18 |
Family
ID=15531842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55152045A Granted JPS5776766A (en) | 1980-10-31 | 1980-10-31 | Fuel cell powder generator |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5776766A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06105625B2 (en) * | 1984-12-21 | 1994-12-21 | 株式会社東芝 | Molten carbonate fuel cell |
| JPH0170267U (en) * | 1987-10-29 | 1989-05-10 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5563B2 (en) * | 1974-09-26 | 1980-01-05 | ||
| JPS52188U (en) * | 1975-06-19 | 1977-01-05 |
-
1980
- 1980-10-31 JP JP55152045A patent/JPS5776766A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5776766A (en) | 1982-05-13 |
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