JPS62229767A - Fuel cell - Google Patents
Fuel cellInfo
- Publication number
- JPS62229767A JPS62229767A JP61072849A JP7284986A JPS62229767A JP S62229767 A JPS62229767 A JP S62229767A JP 61072849 A JP61072849 A JP 61072849A JP 7284986 A JP7284986 A JP 7284986A JP S62229767 A JPS62229767 A JP S62229767A
- Authority
- JP
- Japan
- Prior art keywords
- plate
- cooling
- graphite
- cooling plate
- fuel cell
- 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.)
- Pending
Links
- 239000000446 fuel Substances 0.000 title claims description 12
- 238000001816 cooling Methods 0.000 claims abstract description 65
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000010439 graphite Substances 0.000 claims abstract description 25
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 25
- 239000000853 adhesive Substances 0.000 claims abstract description 20
- 230000001070 adhesive effect Effects 0.000 claims abstract description 20
- 229910021397 glassy carbon Inorganic materials 0.000 claims abstract description 5
- 239000003822 epoxy resin Substances 0.000 claims abstract 3
- 229920000647 polyepoxide Polymers 0.000 claims abstract 3
- 239000007789 gas Substances 0.000 claims description 12
- 239000002737 fuel gas Substances 0.000 claims description 10
- 230000001590 oxidative effect Effects 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000003792 electrolyte Substances 0.000 claims description 7
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 4
- 229910052709 silver Inorganic materials 0.000 claims description 4
- 239000004332 silver Substances 0.000 claims description 4
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 2
- 239000004840 adhesive resin Substances 0.000 claims description 2
- 229920006223 adhesive resin Polymers 0.000 claims description 2
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 abstract description 12
- 239000011347 resin Substances 0.000 abstract description 12
- 239000002245 particle Substances 0.000 abstract description 5
- 239000011230 binding agent Substances 0.000 abstract description 3
- 230000003247 decreasing effect Effects 0.000 abstract 1
- 239000011159 matrix material Substances 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000010248 power generation Methods 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920006332 epoxy adhesive Polymers 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000013011 mating Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
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
- H01M8/04067—Heat exchange or temperature measuring elements, thermal insulation, e.g. heat pipes, heat pumps, fins
- H01M8/04074—Heat exchange unit structures specially adapted for fuel cell
-
- 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)
Abstract
Description
【発明の詳細な説明】
[発明の技術分野〕
本発明は燃料電池に係り、特に集電及び冷却機能を有す
る冷却プレートの構成を改良した燃料電池に関する。DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to a fuel cell, and more particularly to a fuel cell having an improved configuration of a cooling plate having current collection and cooling functions.
[発明の技術的背景]
従来、燃料の有している化学的エネルギーを直接電気的
エネルギーに変換する装置として燃料電。[Technical Background of the Invention] Conventionally, fuel electricity has been used as a device that directly converts chemical energy contained in fuel into electrical energy.
池(以下、単に電池と称する)が知られている。2. Description of the Related Art Cells (hereinafter simply referred to as batteries) are known.
この電池は通常、電解質層を挾んで一対の多孔質の電極
を配置するとともに、一方の電極の背面に水素ガスを供
給する燃料ガスを接触させ、また他方の電極の背面に酸
素ガスのような酸化剤ガスを接触させ、このとき起こる
電気化学的反応を利用して、両電極間から高いエネルギ
ーの変換効率で電気エネルギーを取り出すことができる
ものである。This battery usually has a pair of porous electrodes sandwiching an electrolyte layer, and the back of one electrode is contacted with a fuel gas that supplies hydrogen gas, and the back of the other electrode is contacted with a fuel gas that supplies hydrogen gas. By bringing an oxidizing gas into contact and utilizing the electrochemical reaction that occurs, electrical energy can be extracted from between both electrodes with high energy conversion efficiency.
ところで、上記の原理に基づく、特にりん酸(H3PO
4)を電解質とした電池を構成する単位セルは次のよう
に形成される。すなわち、第3図に示すように単位セル
は電解質を含浸した電解質層(以下、マトリックスと称
する)1を境にして、両側に炭素多孔質で形成され夫々
マトリックス1側に触媒層2,2aが付加されている一
対の電極3.38を配設する。ざらに、両電極3,3a
のマトリックス1との背面側には夫々溝及び凸部となる
リブ4の付いたプレート5(以下、インターコネクタと
称する)を配置する。このインターコネクタ5の各電極
側に位置する面には、夫夫リブ4によって互いに直交す
るような向きに夫夫溝が複I2個互いに平行に形成され
る。インターコネクタ5の片側の面の溝7は燃料ガスの
流通路となり、他の側の面の直交する向きに形成された
溝8は酸化剤ガスの流通路となる。このように形成され
たインターコネクタ5を介して複数個の単位セルを積層
してその上下端部に集電板を配設し、さらに絶縁及び締
付部材を当接して一体に締付けて電池積層体を形成する
。By the way, based on the above principle, especially phosphoric acid (H3PO
A unit cell constituting a battery using 4) as an electrolyte is formed as follows. That is, as shown in FIG. 3, a unit cell is formed of carbon porous material on both sides of an electrolyte layer (hereinafter referred to as matrix) 1 impregnated with an electrolyte, and catalyst layers 2 and 2a are formed on each side of the matrix 1. An additional pair of electrodes 3.38 is provided. Roughly, both electrodes 3, 3a
A plate 5 (hereinafter referred to as an interconnector) having a rib 4 serving as a groove and a convex portion is disposed on the back side of the matrix 1 . On the surface of the interconnector 5 located on the electrode side, two parallel grooves are formed by the groove ribs 4 so as to be perpendicular to each other. A groove 7 on one side of the interconnector 5 serves as a flow path for fuel gas, and a groove 8 formed in an orthogonal direction on the other side serves as a flow path for oxidizing gas. A plurality of unit cells are stacked via the interconnector 5 formed in this way, current collecting plates are arranged at the upper and lower ends thereof, and insulating and tightening members are brought into contact and tightened together to stack the cells. form the body.
そして、第4図に示すようにこの電池積層体の互いに対
向する面に反応ガス供給容器(以下、マニホールドと称
する)を配設する。一方の対向したマニホールド9,9
aは燃料ガスを供給及び排出し、他方の対向したマニホ
ールド10.10aは酸化剤ガスを供給及び排出し、上
述のインターコネクタ5の夫々の溝に両ガスを夫々流通
させる。Then, as shown in FIG. 4, reaction gas supply containers (hereinafter referred to as manifolds) are arranged on mutually opposing surfaces of this battery stack. One opposing manifold 9,9
a supplies and discharges fuel gas, and the other opposed manifold 10.10a supplies and discharges oxidant gas, allowing both gases to flow through respective grooves of the interconnector 5 described above.
このようにしてインターコネクタ形の電池が構成される
。In this way, an interconnector type battery is constructed.
一方、この他にリブ付電極形の電池がある。この電池は
第5図に示すように、前述のインターコネクタ5をセパ
レータ11とリブ4とに分割して構成する。すなわち、
マトリックス1の両側に、触媒層2,2aを形成したリ
ブ付電極12.12aを配設して単位セルを形成する。On the other hand, there is also a ribbed electrode type battery. As shown in FIG. 5, this battery is constructed by dividing the aforementioned interconnector 5 into a separator 11 and a rib 4. That is,
Ribbed electrodes 12.12a having catalyst layers 2, 2a formed thereon are arranged on both sides of the matrix 1 to form a unit cell.
そして、リブ付電極12.12aのマトリックス1と接
する反対側に、溝7,8及びリブ4を形成し、両電極の
溝7.8及びリブ4は互いに直交する方向に形成されて
いることはインターコネクタと同様である。Grooves 7, 8 and ribs 4 are formed on the opposite side of the ribbed electrode 12.12a that contacts the matrix 1, and the grooves 7, 8 and ribs 4 of both electrodes are formed in directions perpendicular to each other. Similar to interconnector.
この単位セルを複数個積層する際に、両ガスの混合を防
ぐためにプレート、すなわち板状のセパレータ11を介
して積層し、前述と同様にして電池積層体を形成してこ
の電池積層体にそれぞれマニホールドを取付けてリブ付
電極形の電池を構成する。When stacking a plurality of unit cells, they are stacked with a plate, that is, a plate-shaped separator 11 interposed therebetween, to prevent mixing of both gases, and a battery stack is formed in the same manner as described above. Attach the manifold to configure a ribbed electrode type battery.
上述のように構成されたインターコネクタ形及びリブ付
電極形の電池にあっては、運転時における単位セル部分
の発熱による温度上昇のために触媒層の劣化などによる
性能低下が起こる。そこでこれを防止するために、イン
ターコネクタ形の電池にあっては第6図に示すように数
個の単位セル毎に、インターコネクタ5に冷却管13が
埋め込まれたインターコネクタ形冷却プレート14を配
設する。また、リブ付電極形の電池にあっては第7図に
示すように数個の単位セル毎に、セパレータ11に冷却
管13が埋め込まれたセパレータ形冷却プレート15を
配設する。このようにして、単位セル内部の発熱を外部
に取り出して電池温度の過度の上昇を防止するようにし
ている。In the interconnector type and ribbed electrode type batteries configured as described above, performance decreases due to deterioration of the catalyst layer due to temperature rise due to heat generation in the unit cell portion during operation. Therefore, in order to prevent this, in the case of an interconnector type battery, an interconnector type cooling plate 14 with cooling pipes 13 embedded in the interconnector 5 is installed for every several unit cells as shown in FIG. Arrange. Further, in the case of a ribbed electrode type battery, a separator type cooling plate 15 in which a cooling pipe 13 is embedded in the separator 11 is provided for every several unit cells as shown in FIG. In this way, the heat generated inside the unit cell is taken out to the outside to prevent the battery temperature from rising excessively.
[背景技術の問題点]
ところで、上述したようなインターコネクタ形及びセパ
レータ形の電池における冷却プレートとしては、何れも
単位セルの積層方向に高い熱伝導性及び電気伝導性を有
し、また耐りん酸性、耐熱性並びに寸法安定性を有する
ことなどが要求される。このため一般には、熱硬化性の
樹脂と黒鉛粒子を混合成形して得られる黒鉛樹脂板や、
黒鉛板に樹脂を含浸してガスの不浸透化を図った不浸透
黒鉛板に、機械加工して冷却管を伝熱性の接着剤で埋め
込み固定し、更に埋め込み接着剤の電池雰囲気曝露劣化
防止、冷却プレート表面の15〜20%を占める接着剤
部の高熱抵抗部の伝熱不均化を緩和するために、同じ部
材の合せ板を導電性の高い接着剤で貼り合せることによ
り冷却プレートを形成している。[Problems with the Background Art] By the way, cooling plates for interconnector type and separator type batteries as described above both have high thermal conductivity and electrical conductivity in the stacking direction of unit cells, and are resistant to phosphorescence. It is required to have acidity, heat resistance, and dimensional stability. For this reason, graphite resin plates obtained by mixing and molding thermosetting resin and graphite particles,
The impermeable graphite plate is impregnated with resin to make it impermeable to gas, and the cooling tube is machined and fixed by embedding it with a heat conductive adhesive, and the embedded adhesive is also prevented from deteriorating when exposed to the battery atmosphere. In order to alleviate heat transfer imbalance in the high heat resistance part of the adhesive part, which accounts for 15 to 20% of the cooling plate surface, the cooling plate is formed by bonding plates of the same material with a highly conductive adhesive. are doing.
しかしながら、上述のような熱硬化性樹脂と黒鉛粒子の
混合成形材である黒鉛樹脂板または不浸透黒鉛板では、
冷却プレートの合せ板は500X500#+m以上の大
形のものにおいてその厚さを3M以下にすることは、作
業上破損が発生することから非常に困難である。この結
果、冷却プレートの厚みが大きくなることから、電池本
体内での一定積層当りの高さが高くなって電池が大形な
ものになるという問題がある。また、冷却プレートの厚
みが大きいことからその重lが大きくなり、結果的に電
池本体の重量が増加するという問題がある。However, in the graphite resin plate or impermeable graphite plate which is a mixed molding material of thermosetting resin and graphite particles as described above,
It is very difficult to reduce the thickness of the cooling plate to 3M or less in a large-sized cooling plate of 500×500#+m or more because damage may occur during work. As a result, since the thickness of the cooling plate increases, the height per certain number of layers within the battery body increases, resulting in a problem that the battery becomes larger. Furthermore, since the thickness of the cooling plate is large, its weight becomes large, resulting in an increase in the weight of the battery body.
[発明の目的]
本発明は上記のような問題を解決するために成されたも
ので、その目的とするところは冷却プレートの厚みを小
さくして装置の小形化ならびに軽S化を図ることが可能
な信頼性の高い燃料電池を提供することにある。[Object of the Invention] The present invention was made to solve the above-mentioned problems, and its purpose is to reduce the thickness of the cooling plate and thereby reduce the size and weight of the device. Our goal is to provide the most reliable fuel cell possible.
[発明の概要]
上記目的を達成するために本発明では、電解質層を挾ん
で一対の電極を配置すると共に、一方の電極の背面に燃
料ガスをまた他方の電極の背面に酸化剤ガスを夫々流通
させて電気エネルギーを出力する単位セルを形成し、上
記燃料ガスと前記酸化剤ガスの混合を防止するとともに
上記単位セルを電気的に接続する機能を有するプレート
を介して上記単位セルを複数個積層し、かつ冷却管を埋
設した冷却プレートを上記所定個の単位セル毎に配設し
て成る燃料電池において、上記冷却プレートとして冷却
管を埋設した黒鉛板からなる第1のプレートと、グラツ
シーカーボン板からなる第2のプレートとを、導電性接
着剤により貼り合せて形成したものを用いるようにした
ことを特徴とする。[Summary of the Invention] In order to achieve the above object, the present invention arranges a pair of electrodes with an electrolyte layer in between, and injects a fuel gas onto the back surface of one electrode and an oxidant gas onto the back surface of the other electrode. A plurality of the unit cells are connected through a plate having a function of forming a unit cell that outputs electrical energy by flowing the fuel gas, preventing mixing of the fuel gas and the oxidizing gas, and electrically connecting the unit cells. In a fuel cell in which stacked cooling plates each having a cooling pipe embedded therein are disposed for each of the predetermined unit cells, the cooling plate includes a first plate made of a graphite plate having a cooling pipe embedded therein; It is characterized in that it uses a plate formed by bonding a second plate made of a carbon plate with a conductive adhesive.
[発明の実施例コ
まず本発明の特徴とするところは、前述した冷却プレー
トを、熱硬化性樹脂と黒鉛粒子を混合し成形して得られ
る黒鉛樹脂板、または黒鉛と結着剤を混合、成形し高温
処理した黒鉛板に樹脂を含浸することによりガスの不浸
透化を図った不浸透黒鉛板に、冷却管理め込み用の溝加
工をして冷却管を伝熱性の高い物質にて埋設してなる第
1のプレートの上に、耐熱・耐食性を有しまた電解質の
浸透も殆んどなく厚みの小さなグラツシーカーポの厚み
を小さくするようにした点にある。[Embodiments of the Invention] First, the characteristics of the present invention are that the above-mentioned cooling plate is a graphite resin plate obtained by mixing and molding a thermosetting resin and graphite particles, or a graphite resin plate obtained by mixing graphite and a binder, The impermeable graphite plate is made impervious to gas by impregnating the graphite plate with resin, which has been molded and treated at high temperatures. Grooves for cooling management are embedded in the impermeable graphite plate, and cooling pipes are buried in a material with high heat conductivity. On top of the first plate formed by the above structure, the thickness of the Grassy Capo, which has heat resistance and corrosion resistance and is hardly penetrated by electrolyte and has a small thickness, is made small.
以下、本発明を図面に示す具体的な一実施例に基づいて
説明する。The present invention will be described below based on a specific embodiment shown in the drawings.
第1図は、本発明による冷却プレートの構成例を斜視図
にて示したものである。図において、黒鉛粒子をピッチ
を結着剤として成形したものを2000℃で黒鉛化処理
し、その後、減圧下で樹脂を含浸した600X700口
の不浸透黒鉛板16に冷却管埋込用7m!17を形成す
る。次に、冷却管18をカーボンエポキシ導電接着剤1
9を用いて上記冷却管埋込用溝17に埋め込み硬化固定
させて第1のプレートを形成させる。ざらにこの第1の
プレートの上に600jmX 700amX 1 sa
tなる形状のグラッシーカーボン板20を合せ板つまり
第2のプレートとして、銀エポキシ導電接着剤2)に貼
り合せることにより冷却プレートを形成する。第2図に
、かかる冷却プレートの断面図を示している。FIG. 1 is a perspective view showing an example of the configuration of a cooling plate according to the present invention. In the figure, graphite particles are molded using pitch as a binder, graphitized at 2000°C, and then impregnated with resin under reduced pressure on a 600 x 700 impermeable graphite plate 16 for embedding cooling pipes. form 17. Next, connect the cooling pipe 18 with carbon epoxy conductive adhesive 1.
9 is used to embed it in the cooling pipe embedding groove 17 and harden and fix it to form the first plate. Roughly place 600 m x 700 am x 1 sa on top of this first plate.
A cooling plate is formed by bonding a glassy carbon plate 20 having a shape t as a second plate to a silver epoxy conductive adhesive 2). FIG. 2 shows a cross-sectional view of such a cooling plate.
次に表1は本実施例による冷却プレートの形状寸法を示
すものであり、併せて従来の冷却プレートについても示
している。Next, Table 1 shows the shape and dimensions of the cooling plate according to this embodiment, and also shows the conventional cooling plate.
[表1]
表1から明らかなように本実施例によれば、冷却プレー
ト1枚について約2)I11だけ厚さを従来のものより
も薄くすることができる。このことは、大容量の400
セル積層の電池の場合、5セルにつき1枚の冷却プレー
トが配設されるとすると、従来のものに比して約160
111I11だけ積層高さを低減することができること
を意味するものである。[Table 1] As is clear from Table 1, according to this embodiment, the thickness of one cooling plate can be made thinner by about 2) I11 than the conventional one. This means that the large capacity 400
In the case of a battery with stacked cells, if one cooling plate is provided for every 5 cells, the cooling plate will be approximately 160% lower than the conventional one.
This means that the stack height can be reduced by 111I11.
一方、表2は冷却プレートの軽量化について調べた結果
を、本実施例による合せ板の重量および従来の合せ板の
重量について夫々示したものである。On the other hand, Table 2 shows the results of an investigation into the weight reduction of the cooling plate, regarding the weight of the laminated plate according to this example and the weight of the conventional laminated plate, respectively.
[表2]
表2から明らかなように本実施例によれば、600X7
00m形状の冷却プレート1枚当り、約1.64Kgの
軽】化を図ることができる。このことは、上述の400
セル積層の電池の場合に、約130Kgだけの軽量化を
図ることが可能となることを意味するものである。[Table 2] As is clear from Table 2, according to this example, 600X7
It is possible to reduce the weight by approximately 1.64 kg per 00m-shaped cooling plate. This corresponds to the 400
This means that in the case of a cell stack battery, it is possible to reduce the weight by about 130 kg.
なお、本実施例による冷却プレートを電池に組み込んで
発電試験を行なった結果、従来の冷却プレートを組み込
んだものと冷却性能の差は認められなかった。Incidentally, as a result of a power generation test conducted by incorporating the cooling plate according to this example into a battery, no difference in cooling performance was observed compared to a battery incorporating a conventional cooling plate.
か(して、本実施例の冷却プレートを組み込んだ電池に
よれば、従来のような冷却プレートに比して電気伝導度
の低下が少ないために、運転による冷却プレートの合せ
界面のオーム損の増大はなく、また熱抵抗の増大による
冷却効率の低下がなく、結果的に高い一定した発電効率
を得ることができる。また、冷却プレートの厚みを小さ
くすることができることから、電池本体での一定積層当
りの高さを低くして電池の小形化を図ることが可能であ
る。さらに、上記理由により冷却プレート重量を小さく
できることから、結果的に電池本体の軽量化を図ること
が可能である。(Thus, according to the battery incorporating the cooling plate of this example, the decrease in electrical conductivity is smaller than that of a conventional cooling plate, so that the ohmic loss at the mating interface of the cooling plate due to operation is reduced. There is no increase in cooling efficiency, and there is no decrease in cooling efficiency due to an increase in thermal resistance, resulting in a high and constant power generation efficiency.Also, since the thickness of the cooling plate can be reduced, a constant power generation efficiency in the battery body can be achieved. It is possible to reduce the size of the battery by lowering the height per layer.Furthermore, since the weight of the cooling plate can be reduced for the above-mentioned reason, it is possible to reduce the weight of the battery body as a result.
尚、上記実施例では導電性接着剤としてカーボンエポキ
シ接着剤および銀エポキシ接着剤を用いた例について述
べたが、かかる接着剤は接着機能と導電機能を有するも
のであれば上記以外の接着剤、例えばフェノール系樹脂
の接着樹脂からなるものであってもよいものである。In the above embodiment, carbon epoxy adhesive and silver epoxy adhesive were used as conductive adhesives, but such adhesives may be adhesives other than those mentioned above as long as they have an adhesive function and a conductive function. For example, it may be made of an adhesive resin such as a phenolic resin.
また、上記実施例では第1のプレートとして不浸透黒鉛
板を用いたが、これに限らず前述したような黒鉛樹脂板
を用いるようにしてもよいものである。Further, in the above embodiment, an impermeable graphite plate is used as the first plate, but the present invention is not limited to this, and a graphite resin plate as described above may also be used.
その他、本発明はその要旨を変更しない範囲で、種々変
形して実施することができるものである。In addition, the present invention can be implemented with various modifications without changing the gist thereof.
[発明の効果]
以上説明したように本発明によれば、冷却プレートとし
て、冷却管を埋設した黒鉛板からなる第1のプレートと
、グラッシーカーボン板からなる第2のプレートを、導
電性接着剤により貼り合せて形成したものを用いて構成
するようにしたので、冷却プレートの厚みを小さくして
装置の小形化ならびにlll化を図ることが可能な極め
て信頼性の高い燃料電池が提供できる。[Effects of the Invention] As explained above, according to the present invention, the first plate made of a graphite plate with cooling pipes embedded therein and the second plate made of a glassy carbon plate are bonded with a conductive adhesive. Since the structure is made using a material bonded together, it is possible to provide an extremely reliable fuel cell in which the thickness of the cooling plate can be reduced and the device can be made smaller and more compact.
第1図は本発明の一実施例による冷却プレートを示す斜
視図、第2図は同実施例による冷却プレートを示す断面
図、第3図は電池の単位セルを示す分解斜視図、第4図
は同単位セルを組み込んだ電池を示す斜視図、第5図は
電池の単位セルを示す分解斜視図、第6図は冷却プレー
トと単位セルを示す分解斜視図、第7図は冷却プレート
と単位セルを示す分解斜視図である。
14・・・インターコネクタ形冷却プレート、15・・
・セパレータ形冷却プレート、16・・・不浸透黒鉛板
、17・・・冷却管埋込用溝、18・・・冷却管、19
・・・カーボンエポキシ導電性接着剤、20・・・グラ
ツシーカーボン板、2)・・・銀エポキシ導電性接着剤
。
出願人代理人 弁理士 鈴江武彦
第1r7I
第2図
第3図
a
第4図
第5 図FIG. 1 is a perspective view showing a cooling plate according to an embodiment of the present invention, FIG. 2 is a sectional view showing a cooling plate according to the same embodiment, FIG. 3 is an exploded perspective view showing a unit cell of a battery, and FIG. 4 is a perspective view showing a battery incorporating the same unit cell, FIG. 5 is an exploded perspective view showing the unit cell of the battery, FIG. 6 is an exploded perspective view showing the cooling plate and the unit cell, and FIG. 7 is the cooling plate and unit. It is an exploded perspective view showing a cell. 14... Interconnector type cooling plate, 15...
・Separator type cooling plate, 16... Impermeable graphite plate, 17... Cooling pipe embedding groove, 18... Cooling pipe, 19
...Carbon epoxy conductive adhesive, 20...Gratsy carbon plate, 2)...Silver epoxy conductive adhesive. Applicant's agent Patent attorney Takehiko Suzue No. 1r7I Figure 2 Figure 3a Figure 4 Figure 5
Claims (1)
一方の電極の背面に燃料ガスまた他方の電極の背面に酸
化剤ガスを夫々流通させて電気エネルギーを出力する単
位セルを形成し、前記燃料ガスと前記酸化剤ガスの混合
を防止するとともに前記単位セルを電気的に接続する機
能を有するプレートを介して前記単位セルを複数個積層
し、かつ冷却管を埋設した冷却プレートを前記所定個の
単位セル毎に配設して成る燃料電池において、前記冷却
プレートとして、冷却管を埋設した黒鉛板からなる第1
のプレートと、グラッシーカーボン板からなる第2のプ
レートとを、導電性接着剤により貼り合せて形成したも
のを用いるようにしたこ■を特徴とする燃料電池。 ■■■導電性接着剤は、カーボン又は銀のうちの■■■
■一種類又はこれらの混合物を充填剤とすることを特徴
とする特許請求の範囲第(1)項記載の燃料電池。 (3)導電性接着剤は、フェノール系樹脂又はエポキシ
系樹脂の接着樹脂からなることを特徴とする特許請求の
範囲第(1)項または第(2)項記載の燃料電池。[Claims] (1) A pair of electrodes are arranged with an electrolyte layer sandwiched between them, and
A unit cell that outputs electrical energy is formed by flowing a fuel gas on the back surface of one electrode and an oxidizing gas on the back surface of the other electrode to prevent mixing of the fuel gas and the oxidizing gas and to prevent the unit cell from flowing between the fuel gas and the oxidizing gas. In the fuel cell, a plurality of the unit cells are stacked via plates having a function of electrically connecting the cells, and a cooling plate in which cooling pipes are embedded is arranged for each of the predetermined number of unit cells, As a cooling plate, the first plate is made of a graphite plate with cooling pipes embedded in it.
2. A fuel cell characterized in that it uses a plate formed by bonding the plate and a second plate made of a glassy carbon plate with a conductive adhesive. ■■■ Conductive adhesive is either carbon or silver ■■■
(2) The fuel cell according to claim (1), characterized in that one kind or a mixture thereof is used as a filler. (3) The fuel cell according to claim (1) or (2), wherein the conductive adhesive is made of an adhesive resin such as a phenolic resin or an epoxy resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61072849A JPS62229767A (en) | 1986-03-31 | 1986-03-31 | Fuel cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61072849A JPS62229767A (en) | 1986-03-31 | 1986-03-31 | Fuel cell |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62229767A true JPS62229767A (en) | 1987-10-08 |
Family
ID=13501237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61072849A Pending JPS62229767A (en) | 1986-03-31 | 1986-03-31 | Fuel cell |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62229767A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006156173A (en) * | 2004-11-30 | 2006-06-15 | Nissan Motor Co Ltd | Separator for fuel cell using pipe material, manufacturing method of fuel cell and separator for fuel cell |
-
1986
- 1986-03-31 JP JP61072849A patent/JPS62229767A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006156173A (en) * | 2004-11-30 | 2006-06-15 | Nissan Motor Co Ltd | Separator for fuel cell using pipe material, manufacturing method of fuel cell and separator for fuel cell |
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