JPH0325901B2 - - Google Patents
Info
- Publication number
- JPH0325901B2 JPH0325901B2 JP59151244A JP15124484A JPH0325901B2 JP H0325901 B2 JPH0325901 B2 JP H0325901B2 JP 59151244 A JP59151244 A JP 59151244A JP 15124484 A JP15124484 A JP 15124484A JP H0325901 B2 JPH0325901 B2 JP H0325901B2
- Authority
- JP
- Japan
- Prior art keywords
- electrolyte
- matrix
- thin film
- battery
- electrode
- 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 - Lifetime
Links
- 239000003792 electrolyte Substances 0.000 claims description 31
- 239000011159 matrix material Substances 0.000 claims description 28
- 239000010409 thin film Substances 0.000 claims description 18
- 239000000446 fuel Substances 0.000 claims description 7
- 239000007789 gas Substances 0.000 claims description 5
- 239000002737 fuel gas Substances 0.000 claims description 4
- 238000007599 discharging Methods 0.000 claims 1
- 230000002093 peripheral effect Effects 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 238000009792 diffusion process Methods 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 125000006850 spacer group Chemical group 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- -1 polytetrafluoroethylene Polymers 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 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
- H01M8/02—Details
- H01M8/0289—Means for holding the electrolyte
- H01M8/0293—Matrices for immobilising electrolyte solutions
-
- 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
- H01M8/04276—Arrangements for managing the electrolyte stream, e.g. heat exchange
- H01M8/04283—Supply means of electrolyte to or in matrix-fuel cells
-
- 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】
〔発明の利用分野〕
本発明は、燃料電池に係り、特に、単位料池構
成の中でマトリツクスの取り扱いの簡略化と外部
からマトリツクス層内に電解質を補給する構造に
関する。[Detailed Description of the Invention] [Field of Application of the Invention] The present invention relates to a fuel cell, and particularly relates to a structure for simplifying the handling of a matrix in a unit fuel cell configuration and for replenishing electrolyte from the outside into a matrix layer. .
一般に、燃料電池を構成する単位電池は、第1
図に示す様に、燃料ガスおよび空気の流通路をも
つガス拡散電極1,2と、これら一対のガス拡散
電極の間にマトリツクス3を配して構成する。こ
の様に構成された単位電池をセパレータ4を介し
て複数個積層して電池本体が構成される。
Generally, the unit cells constituting the fuel cell are the first
As shown in the figure, the structure includes gas diffusion electrodes 1 and 2 having flow paths for fuel gas and air, and a matrix 3 arranged between the pair of gas diffusion electrodes. A battery body is constructed by stacking a plurality of unit batteries configured in this way with separators 4 interposed therebetween.
そこで、従来のマトリツクスは、例えば、炭化
硅素、金属燐酸塩のような無機粉体に電解質であ
る燐酸を加え混練し、スラリー状にしてガス拡散
電極1又は2に塗布して形成していた。この様に
すると、電池締付等によりマトリツクスが電極か
らはみ出してしまい、必要なマトリツクス量が維
持出来なくなり、電池性能に悪影響を及ぼす。こ
のため、電極の端部周縁部にスペーサーを配し
て、マトリツクスのはみ出しを防いでいるが、完
全ではない。また、マトリツクスは濃縮された燐
酸を混合した強酸から成つているスラリーのた
め、塗布作業や電極貼り合せ作業時の取り扱い
方、さらに、濃縮された燐酸は吸湿性が強く、塗
布前のマトリツクススラリーや電極貼り合せ後の
電池の保管法、吸湿対策等の品質管理面からも問
題がある。 Therefore, conventional matrices are formed by adding phosphoric acid as an electrolyte to inorganic powder such as silicon carbide or metal phosphate, kneading the mixture, making a slurry, and applying the slurry to the gas diffusion electrode 1 or 2. If this is done, the matrix will protrude from the electrode due to battery tightening, etc., making it impossible to maintain the required amount of matrix, which will have an adverse effect on battery performance. For this reason, spacers are placed around the edges of the electrodes to prevent the matrix from protruding, but this is not perfect. In addition, since the matrix is a slurry made of strong acid mixed with concentrated phosphoric acid, it is important to know how to handle it during coating work and electrode bonding work.Furthermore, concentrated phosphoric acid has strong hygroscopicity, so the matrix slurry must be mixed with concentrated phosphoric acid. There are also problems in terms of quality control, such as how to store batteries after bonding electrodes, and measures against moisture absorption.
また、別の問題点として、マトリツクス中の電
解質が電池運転中の電池反応に伴う生成水(水蒸
気)と共に外部に飛散し減少して電池性能の低下
ならびに電池寿命が短かくなる恐れがある。そこ
で、電極のガス拡散部分にあらかじめ余分の電解
質をリザーブする方法があるが、この方法では、
燃料ガス、および、空気の拡散を阻害しやすい。
また、外部からの電解質の補給方法はまだ名案が
なく実施までには至つていない。 Another problem is that the electrolyte in the matrix is scattered and reduced to the outside together with the water (steam) generated by the battery reaction during battery operation, leading to a risk of deterioration of battery performance and shortening of battery life. Therefore, there is a method to reserve excess electrolyte in the gas diffusion part of the electrode, but with this method,
Diffusion of fuel gas and air is likely to be inhibited.
Furthermore, there is no good idea yet for how to replenish electrolytes from outside, and this method has not yet been put into practice.
〔発明の目的〕
本発明の目的は、マトリツクス塗布作業を簡略
化して取り扱いを容易にし、電解質を外部からマ
トリツクス層内に補給出来る構造とし、品質の向
上安定化を図ることにある。[Object of the Invention] An object of the present invention is to simplify the matrix coating work and facilitate handling, provide a structure in which electrolyte can be supplied from the outside into the matrix layer, and improve and stabilize quality.
本発明の燃料電池の特徴は、電解質を保持する
ための保持材を多孔質性薄膜を袋状にしてこの内
部に電解質を封入し、これをマトリツクス層とし
て形成させ、さらに、電解質を外部からマトリツ
クス層内に補給する補給口を設けた点にある。
The fuel cell of the present invention is characterized in that the holding material for holding the electrolyte is a porous thin film in the form of a bag, the electrolyte is sealed inside the bag, and this is formed as a matrix layer. The point is that a replenishment port is provided within the layer.
以下、本発明の実施例を図に従つて説明する。
第2図に示す様に多孔質性の薄膜6を二枚配置し
その二枚の端部周縁部の間に無孔質のスペーサー
7を配置し、それぞれが接着されている。さら
に、スペーサー7の端部に電解質封入口並びに外
部から電解質補給のための補給口8を貫通させて
接続管が設けられている。第2図では、この電解
質封入口並びに補給口は四ケ所になつているが、
特に、設置する場所と数員には特に制限はない。
すなわち、第3図に示す様に、多孔質性薄膜6の
内部に封入された電解質3が薄膜の細孔を通過し
電極側に到達し、燃料ガスおよび空気と接触して
電池反応が起こる。この様なマトリツクス層を形
成することによつて単位電池組立時のマトリツク
ス塗布作業は薄膜で構成された袋状のものを電極
上に配し、単位電池積層時、または電池本体積層
終了時に、例えば、定量吐出装置等を使用して圧
入することによつて設定量の電解質を封入できる
ので、同一条件での作業が可能となりマトリツク
スの取り扱いが容易になり、また、品質の安定化
が図れる。
Embodiments of the present invention will be described below with reference to the drawings.
As shown in FIG. 2, two porous thin films 6 are arranged, and a non-porous spacer 7 is arranged between the edges of the two films, and each of them is adhered. Further, a connecting pipe is provided at the end of the spacer 7 so as to pass through an electrolyte sealing port and a replenishing port 8 for replenishing electrolyte from the outside. In Figure 2, there are four electrolyte filling ports and replenishment ports.
In particular, there are no particular restrictions on the installation location or the number of people.
That is, as shown in FIG. 3, the electrolyte 3 sealed inside the porous thin film 6 passes through the pores of the thin film, reaches the electrode side, contacts the fuel gas and air, and a cell reaction occurs. By forming such a matrix layer, the matrix coating operation when assembling the unit cells involves placing a bag-shaped thin film on the electrodes, and applying the matrix at the time of stacking the unit cells or when the stacking of the main batteries is finished, for example. Since a set amount of electrolyte can be sealed by press-fitting using a quantitative dispensing device or the like, it is possible to work under the same conditions, making it easier to handle the matrix and stabilizing the quality.
ここで、封入される電解質は、電極側への電解
質の透過量を薄膜の細孔径によつて制御すること
が出来るので、電解質である燐酸のみを封入する
ことが出来る。また、従来のマトリツクスである
粉体に電解質を含浸したスラリーを封入しても何
ら影響はない。そこで、前述薄膜の細孔径として
は、電極のぬれ現象を生じさせ、電池反応を阻害
させないためには、40μ以下でガス透過率で50
ml/cm2/sec以上が望ましい。この様に、薄膜で
形成した袋状の内部に電解質を封入しても常圧で
は薄膜の内部にとどまることになる。そして、電
池締付圧力によつて、薄膜の細孔部から電解質が
にじみ出て来て前述のように電極内で反応ガスと
接触し、電池反応が起こる。この薄膜の材質は、
耐酸性、耐熱性が要求される。例えば、ふつ素樹
脂系のPTFE(ポリテトラフルオロエチレン樹脂)
の不織布、または、薄膜状にしたもので、第3図
のスペーサー7は無孔質のPTFEを使用する。こ
の様にすることにより、マトリツクス層の端部周
縁部から電解質の漏れを防止することが出来る。
また、この多孔質性薄膜の厚さが厚くなると、電
池内部抵抗が大きくなり、電池性能の低下をもた
らすため、出来る限り薄い方が良いが薄膜の強度
等を考慮すれば25〜100μ程度が望ましい。 Here, the amount of electrolyte to be sealed can be controlled by the pore diameter of the thin film to control the amount of electrolyte that permeates to the electrode side, so only phosphoric acid, which is the electrolyte, can be sealed. Further, even if a slurry impregnated with an electrolyte is enclosed in a powder which is a conventional matrix, there is no effect at all. Therefore, the pore diameter of the thin film mentioned above must be 40μ or less to cause wetting of the electrodes and prevent the battery reaction from being inhibited.
ml/cm 2 /sec or more is desirable. In this way, even if an electrolyte is sealed inside a bag-shaped interior formed of a thin film, it will remain inside the thin film at normal pressure. Then, due to the battery clamping pressure, the electrolyte oozes out from the pores of the thin film and comes into contact with the reaction gas within the electrode as described above, causing a battery reaction. The material of this thin film is
Acid resistance and heat resistance are required. For example, fluorine resin PTFE (polytetrafluoroethylene resin)
The spacer 7 shown in FIG. 3 uses non-porous PTFE. By doing so, leakage of electrolyte from the edge portion of the matrix layer can be prevented.
Also, as the thickness of this porous thin film increases, the internal resistance of the battery increases, leading to a decrease in battery performance, so it is better to be as thin as possible, but when considering the strength of the thin film, it is preferably about 25 to 100μ. .
第4図は、前述した電解質封入口9が外部電解
質補給槽10がマニホールド5を介して接続され
ている。外部電解質槽には、常時、適当な圧力を
加える様にすれば電解質は、常に、マトリツクス
槽内部に補給され、電池運転による電解質の飛散
減少がなくなり、電池性能の安定と長寿命化を図
ることが出来る。本実施例の様にすることによつ
て、マトリツクスの塗布作業が簡略化され、さら
に、外部からの電解質補給が容易に出来る構造に
なり品質向上と安定化を図ることが出来る。 In FIG. 4, the electrolyte sealing port 9 described above is connected to an external electrolyte replenishing tank 10 via a manifold 5. By applying appropriate pressure to the external electrolyte tank at all times, the electrolyte will always be replenished inside the matrix tank, eliminating the loss of electrolyte scattering due to battery operation, and stabilizing battery performance and extending the lifespan. I can do it. By doing as in this embodiment, the matrix application work is simplified, and furthermore, the structure allows easy replenishment of electrolyte from the outside, thereby improving quality and stabilizing the structure.
本発明によれば、電解質保持を多孔質性薄膜で
構成したことにより、マトリツクスの取り扱いが
容易となり、また、マニホールドの外部から電解
質補給路が簡単に構成できる。
According to the present invention, since the electrolyte is retained using a porous thin film, handling of the matrix becomes easy, and an electrolyte replenishment path can be easily constructed from outside the manifold.
第1図は、従来の電池の斜視図、第2図は本発
明によるマトリツクス層の構成斜視図、第3図は
第1図のマトリツクスを単位電池に構成した斜視
図、第4図はマトリツクス層内に電解質を補給す
る構成図である。
6……多孔質性薄膜、7……スペーサー、8…
…電解質封入口、9……接続管。
Fig. 1 is a perspective view of a conventional battery, Fig. 2 is a perspective view of the structure of a matrix layer according to the present invention, Fig. 3 is a perspective view of the matrix of Fig. 1 configured into a unit battery, and Fig. 4 is a perspective view of the matrix layer. FIG. 6... Porous thin film, 7... Spacer, 8...
...Electrolyte sealing port, 9...Connection pipe.
Claims (1)
間にマトリツクスを挾み、これを単位電池として
セパレータを介して複数個積み重ね、この電池の
側面に燃料ガスおよび空気を供給排出するための
マニホールドを配した燃料電池において、 前記マトリツクスを薄膜で袋状に形成するとと
もに、この薄膜を多孔質にしてこの内部に電解質
を封入したことを特徴とする燃料電池。 2 特許請求の範囲第1項において、 前記多孔質性薄膜で形成した前記マトリツクス
の周縁部に前記電解質の補給口を設けたことを特
徴とする燃料電池。[Claims] 1. A matrix is sandwiched between a fuel electrode and an air electrode that have opposing gas flow paths, and a plurality of these are stacked up as unit cells with separators interposed therebetween, and fuel gas and air are placed on the sides of the cells. 1. A fuel cell equipped with a manifold for supplying and discharging the matrix, characterized in that the matrix is formed into a bag shape using a thin film, the thin film is made porous, and an electrolyte is sealed inside. 2. The fuel cell according to claim 1, wherein a replenishment port for the electrolyte is provided at a peripheral edge of the matrix formed of the porous thin film.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59151244A JPS6132359A (en) | 1984-07-23 | 1984-07-23 | Fuel cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59151244A JPS6132359A (en) | 1984-07-23 | 1984-07-23 | Fuel cell |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6132359A JPS6132359A (en) | 1986-02-15 |
| JPH0325901B2 true JPH0325901B2 (en) | 1991-04-09 |
Family
ID=15514410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59151244A Granted JPS6132359A (en) | 1984-07-23 | 1984-07-23 | Fuel cell |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6132359A (en) |
-
1984
- 1984-07-23 JP JP59151244A patent/JPS6132359A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6132359A (en) | 1986-02-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |