JP3240062B2 - Method for manufacturing fuel cell separator with end seal - Google Patents

Method for manufacturing fuel cell separator with end seal

Info

Publication number
JP3240062B2
JP3240062B2 JP07225091A JP7225091A JP3240062B2 JP 3240062 B2 JP3240062 B2 JP 3240062B2 JP 07225091 A JP07225091 A JP 07225091A JP 7225091 A JP7225091 A JP 7225091A JP 3240062 B2 JP3240062 B2 JP 3240062B2
Authority
JP
Japan
Prior art keywords
separator
fuel cell
end seal
joining
weight
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 - Fee Related
Application number
JP07225091A
Other languages
Japanese (ja)
Other versions
JPH04282565A (en
Inventor
義雄 鈴木
敏治 上井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tokai Carbon Co Ltd
Original Assignee
Tokai Carbon Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tokai Carbon Co Ltd filed Critical Tokai Carbon Co Ltd
Priority to JP07225091A priority Critical patent/JP3240062B2/en
Publication of JPH04282565A publication Critical patent/JPH04282565A/en
Application granted granted Critical
Publication of JP3240062B2 publication Critical patent/JP3240062B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/02Details
    • H01M8/0202Collectors; Separators, e.g. bipolar separators; Interconnectors
    • H01M8/0204Non-porous and characterised by the material
    • H01M8/0213Gas-impermeable carbon-containing materials
    • 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
    • Y02E60/50Fuel cells
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

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】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、炭素質の多孔質電極板
と緻密質セパレータが一体化したリン酸型燃料電池用複
合部材を構成する端部シール付セパレータの製造方法に
関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a separator with an end seal constituting a composite member for a phosphoric acid type fuel cell in which a carbonaceous porous electrode plate and a dense separator are integrated.

【0002】[0002]

【従来の技術】リン酸型燃料電池を形成する電極板、セ
パレータ板等の部材には、材質的に耐熱性、耐薬品性、
良電気伝導性、易加工性などの要求特性を満たす炭素質
材料が有用されている。ところが、炭素質材料は本質的
に機械的強度が低いため、ハンドリングあるいはセルの
組立時に破損することがある。近時、電池内部抵抗およ
びスタック厚みの低下を図るために電極板およびセパレ
ータ板はますます薄肉化が進んでおり、破損の度合は増
加の傾向にある。
2. Description of the Related Art Materials such as an electrode plate and a separator plate forming a phosphoric acid type fuel cell are made of materials having heat resistance, chemical resistance, and the like.
Carbonaceous materials satisfying required characteristics such as good electrical conductivity and easy workability have been used. However, since the carbonaceous material has essentially low mechanical strength, it may be damaged during handling or cell assembly. Recently, in order to reduce the internal resistance of the battery and the thickness of the stack, the electrode plate and the separator plate have been increasingly thinned, and the degree of breakage has been increasing.

【0003】このような問題を解消するために、予め炭
素材で形成された多孔質電極基材とセパレータ基材また
はこれらの前駆体(炭素化前の材料)を接着剤を介して
結合したのち焼成炭化処理する接合焼成法が開発されて
いる(特開昭60-20471号公報、実開昭60-16759号公報)
。しかし、該接合焼成法による場合には電池内部抵抗
を低下させる面では優れた効果を示すものの、炭素部材
の前面を接合し、さらに焼成処理を施こす工程が必要と
なるために、製造コストが著しく高くなる欠点がある。
In order to solve such a problem, a porous electrode substrate previously formed of a carbon material and a separator substrate or a precursor thereof (a material before carbonization) are bonded via an adhesive. A bonding firing method for firing carbonization has been developed (JP-A-60-20471, JP-A-60-16759).
. However, in the case of using the bonding firing method, although an excellent effect is exhibited in terms of lowering the internal resistance of the battery, a step of bonding the front surface of the carbon member and further performing a firing treatment is required, so that the manufacturing cost is reduced. There is the disadvantage that it is significantly higher.

【0004】このため、セパレータの両端部位に端部シ
ール材を耐熱耐蝕性の弗素系樹脂などによって接合し、
形成された凹部に多孔質電極基材を嵌挿するシール接合
法(特開昭62-296368 号公報) が提案されている。
[0004] For this reason, an end sealing material is joined to both end portions of the separator with a heat-resistant and corrosion-resistant fluorine resin or the like.
A seal joining method in which a porous electrode base material is inserted into the formed concave portion (Japanese Patent Application Laid-Open No. 62-296368) has been proposed.

【0005】[0005]

【発明が解決しようとする課題】前記のシール接合法に
よれば、製造工程を大幅に簡略化することが可能となる
が、端部シールの接着強度が十分ではなく、後加工(仕
上げ)時に部材の剥離現象を起こし易い難点がある。そ
のうえ、接合時にホットプレス工程を必要とする煩雑性
があった。
According to the above-mentioned seal joining method, it is possible to greatly simplify the manufacturing process, but the bonding strength of the end seal is not sufficient, and the post-processing (finishing) is difficult. There is a problem that a peeling phenomenon of a member is easily caused. In addition, there is a complication that requires a hot press step at the time of joining.

【0006】本発明は上記従来技術の諸問題を解消する
ために開発されたもので、その目的はシール接合法を採
る場合に端部シール材を十分な気密性、耐ヒートサイク
ル性および耐蝕性を保持した状態で効率よく結合するこ
とができる端部シール付燃料電池セパレータの製造方法
を提供することにある。
SUMMARY OF THE INVENTION The present invention has been developed to solve the above-mentioned problems of the prior art. The purpose of the present invention is to provide an end seal material having sufficient airtightness, heat cycle resistance and corrosion resistance when a seal joining method is employed. It is an object of the present invention to provide a method of manufacturing a fuel cell separator with an end seal, which can efficiently join while holding the fuel cell.

【0007】[0007]

【課題を解決するための手段】上記の目的を達成するた
めの本発明による端部シール付燃料電池セパレータの製
造方法は、ガラス状炭素系セパレータの互いに直交する
表面と裏面の端部に、表面粗さが10μm Rz以上で5〜
300 μm 薄く形成した接合部位を設け、該接合部位にセ
パレータと同材質の端部シール材を平均粒径70μm 以下
のカーボン粉末100 重量部、芳香族ポリイミド前駆体 1
00〜200 重量部およびフェノール樹脂初期縮合物20〜50
重量部からなる組成の接着剤を用いて接合し、熱圧・硬
化させることを構成上の特徴とする。
According to the present invention, there is provided a method of manufacturing a fuel cell separator with an end seal, which comprises the steps of: Roughness of 10μm Rz or more
A 300 μm thin joining portion is provided, and an end sealing material of the same material as the separator is provided at the joining portion with 100 parts by weight of carbon powder having an average particle size of 70 μm or less, and an aromatic polyimide precursor 1
00 to 200 parts by weight and phenol resin precondensate 20 to 50
It is characterized in that it is joined by using an adhesive having a composition consisting of parts by weight, and is heat-pressed and cured.

【0008】セパレータを構成する炭素質材料として
は、耐熱性、耐蝕性、高強度性に加え優れた気体不透過
性を備えるガラス状炭素あるいはこれを基材とする複合
炭素材などガラス状炭素系のものが適用される。したが
って、例えばフェノール系樹脂、フラン系樹脂、ポリイ
ミド樹脂のような樹脂類、もしくは炭素粉末、黒鉛粉
末、炭素繊維チョップ等を混合した前記樹脂類を板状に
成形したのち、焼成炭化処理して得られる材料が該当す
る。
As the carbonaceous material constituting the separator, glassy carbon such as glassy carbon having heat resistance, corrosion resistance, high strength and excellent gas impermeability or a composite carbon material based on the same is used. Applies. Therefore, for example, a resin such as a phenolic resin, a furan resin, a polyimide resin, or a mixture of carbon powder, graphite powder, carbon fiber chop, and the like is molded into a plate shape, and then calcined and carbonized. Applicable materials.

【0009】上記のガラス状炭素系セパレータには、互
いに直交する表面と裏面の各端部(端部シール材の接合
部分)に表面粗さが10μm Rz以上で他のセパレータ部
分よりも5〜300 μm 薄い接合部位を形成する。表面粗
さRzは、JIS B0601(1982)で定められた表面
粗さ基準を指し、この表面粗さを10μm Rz以上に調整
することによって接合面の接着濡れ性が改善され、同時
に接着面積が増大して接着強度が効果的に向上する。薄
肉化した接合面を形成するのは段違い構造に基づく気密
性の向上を図るものであるが、この薄肉度合が5μm 未
満では気密性の改善効果が得られず、他方、300 μm を
越えるとセパレータが破損し易くなる。該接合部位は、
フライス加工のような機械加工により前記範囲に薄肉化
したのち、表面粗さ10μm Rz以上になるようにペーパ
ー仕上げまたはショットブラスト法、サンドブラスト法
等の手段で粗面化する方法で形成することができる。こ
の際、薄肉化をセパレータのグリーン段階(炭素化前)
でおこなってもよく、また前記の粗面加工によって薄肉
化と粗面化を同時におこなうこともできる。
The above-mentioned glassy carbon-based separator has a surface roughness of 10 μm Rz or more at each end (joining portion of the end sealing material) of the front surface and the back surface orthogonal to each other, and is 5 to 300 times higher than the other separator portions. μm Form a thin junction. The surface roughness Rz refers to the surface roughness standard defined in JIS B0601 (1982). By adjusting this surface roughness to 10 μm Rz or more, the adhesion wettability of the bonding surface is improved, and at the same time the bonding area is increased. As a result, the adhesive strength is effectively improved. The purpose of forming a thinned joint surface is to improve the airtightness based on the uneven structure. However, if the thickness is less than 5 μm, the effect of improving the airtightness cannot be obtained. Is easily damaged. The junction is
After the thickness is reduced to the above range by machining such as milling, it can be formed by a method of paper finishing or a surface roughening method such as a shot blast method or a sand blast method so as to have a surface roughness of 10 μm Rz or more. . At this time, the thinning is performed at the green stage of the separator (before carbonization).
Alternatively, the thinning and the roughening can be simultaneously performed by the above-described roughening.

【0010】端部シール材は、前記したセパレータと同
材質のガラス状炭素系材料で構成される。この部材は燃
料電池側部からのガスリークを防止するために機能する
もので、気密性が不完全であると発電効率が低下するほ
か、水素と酸素が混合して爆発の危険が生じる。端部シ
ール材の材質がセパレータと異なると、熱膨張差によっ
て接合界面に剥離、亀裂等が発生して前記の現象を惹起
し易くなる。該端部シール材のサイズは、セパレータの
大きさによっても異なるが、概して幅20〜50mm、厚さ0.
8 〜2.0mm 程度である。なお、端部シール材の接合面に
ついてもセパレータ接合部位と同様の粗面加工を施して
おくと、一層接合強度を増大させることができる。
[0010] The end sealing material is made of a glassy carbon-based material of the same material as the above-mentioned separator. This member functions to prevent gas leakage from the side of the fuel cell. If the airtightness is incomplete, the power generation efficiency is reduced, and hydrogen and oxygen are mixed to cause an explosion. If the material of the end sealing material is different from that of the separator, peeling, cracking, and the like are generated at the joining interface due to the difference in thermal expansion, and the above-mentioned phenomenon is easily caused. The size of the end sealing material varies depending on the size of the separator, but is generally 20 to 50 mm in width and 0.1 mm in thickness.
It is about 8 to 2.0 mm. In addition, if the joining surface of the end sealing material is roughened in the same manner as the separator joining portion, the joining strength can be further increased.

【0011】接着剤の組成は、カーボン粉末 100重量
部、芳香族ポリイミド前駆体 100〜200 重量部およびフ
ェノール樹脂初期縮合物20〜50重量部の配合とする。カ
ーボン粉末には平均粒径70μm 以下のコークス粉、天然
または人造黒鉛粉等が用いられる。芳香族ポリイミド前
駆体としては、ワニス状のポリアミック酸が効果的に使
用される。また、フェノール樹脂初期縮合物は、室温下
で流動性を有するレゾール系のものが好適である。これ
らの3成分は、ニーダー等で均一に混練して接着剤とす
る。
The composition of the adhesive is 100 parts by weight of carbon powder, 100 to 200 parts by weight of an aromatic polyimide precursor, and 20 to 50 parts by weight of a phenol resin precondensate. Coke powder having an average particle size of 70 μm or less, natural or artificial graphite powder, or the like is used as the carbon powder. A varnish-like polyamic acid is effectively used as the aromatic polyimide precursor. Further, the phenol resin precondensate is preferably a resol-based resin having fluidity at room temperature. These three components are uniformly kneaded with a kneader or the like to form an adhesive.

【0012】接合は、前記の接着剤を刷毛塗り法、スプ
レー法、ドクターブレード法など適宜な手段を用いてガ
ラス状炭素系セパレータの接合部位に均一に塗布したの
ち、端部シール材を置いて熱圧しながら接着層を硬化さ
せる方法でおこなわれる。この際、接着層の厚さは50〜
200 μm の範囲にあることが好ましい。また、熱圧操作
には加熱盤付のプレスを用い、温度 100〜250 ℃、加圧
力 0.5〜2kg/cm2の条件を適用することが望ましい。
The bonding is performed by uniformly applying the above-mentioned adhesive to the bonding portion of the vitreous carbon-based separator using an appropriate means such as a brush coating method, a spraying method, a doctor blade method, and then placing an end seal material. This is performed by a method of curing the adhesive layer while applying heat and pressure. At this time, the thickness of the adhesive layer is 50 ~
Preferably it is in the range of 200 μm. It is desirable to use a press equipped with a heating plate for the hot-press operation, and to apply the conditions of a temperature of 100 to 250 ° C. and a pressure of 0.5 to 2 kg / cm 2 .

【0013】接合後、とくにリン酸に接触し易い接合部
分に例えばポリテトラフルオロエチレンのディスパージ
ョンを塗布・硬化してフッ素樹脂の被覆層を形成すると
一層接合部の安定性が向上する。このようにして形成さ
れた接合部材は、最終的に所定の幅、長さおよび厚さに
加工して端部シール付燃料電池セパレータを得る。
After bonding, a dispersion of polytetrafluoroethylene, for example, is applied and cured to a bonding portion which is particularly likely to come into contact with phosphoric acid to form a fluororesin coating layer, thereby further improving the stability of the bonding portion. The joining member thus formed is finally processed into a predetermined width, length and thickness to obtain a fuel cell separator with an end seal.

【0014】[0014]

【作用】本発明では、第1にガラス状炭素系セパレータ
の接合部位を10μm Rz以上に粗面化することで接着性
を高め、更にその部位を5〜300 μm の範囲で薄く形成
することによって段違い接合に基づく気密性の向上を図
る。第2に、セパレータと端部シール材を同一のガラス
状炭素系材質で構成することによって、実用段階での材
質熱膨張差による部材の剥離、亀裂発生などの発生を防
止する。
According to the present invention, first, the bonding portion of the vitreous carbon-based separator is roughened to 10 μm Rz or more to enhance the adhesiveness, and further, the portion is formed thin in the range of 5 to 300 μm. Improve airtightness based on uneven joining. Second, by forming the separator and the end seal material from the same vitreous carbon-based material, it is possible to prevent the members from peeling or cracking due to a difference in thermal expansion of the material in a practical stage.

【0015】第3に、接着剤の成分組成を特定して接合
層の強度、耐熱耐蝕性などを向上させる。すなわち各成
分の機能は、平均粒径70μm 以下のカーボン粉末の配合
は複合効果により接合層に靭性を付与し、芳香族ポリイ
ミド前駆体はフッ素樹脂のように高温高圧をかけずに優
れた接合強度と耐熱耐蝕性を備えるポリイミド樹脂に転
化し、またフェノール樹脂初期縮合物は界面接着力を高
めるために寄与する。
Third, the component composition of the adhesive is specified to improve the strength, heat resistance and corrosion resistance of the bonding layer. In other words, the function of each component is that the compounding of carbon powder with an average particle size of 70 μm or less imparts toughness to the bonding layer due to the combined effect, and the aromatic polyimide precursor has excellent bonding strength without applying high temperature and pressure unlike fluororesin. And a polyimide resin having heat and corrosion resistance, and the phenol resin precondensate contributes to increase interfacial adhesion.

【0016】このような作用が相乗してセパレータの互
いに直交する両面端部に強固かつ気密性よく端部シール
材が一体に接合され、実用段階においても長期安定な端
部シール付燃料電池セパレータを得ることが可能とな
る。
By synergistically acting together, an end sealing material is firmly and airtightly joined to both ends of the separator which are orthogonal to each other, so that a fuel cell separator with an end seal that is stable for a long period of time even in a practical use stage. It is possible to obtain.

【0017】[0017]

【実施例】以下、本発明の実施例を比較例と対比して説
明する。 実施例1〜7、比較例1〜9 平均粒径7μm の黒鉛微粉末をフェノール樹脂に添加混
練し、圧延成形したのち1300℃の温度で焼成炭化処理し
た縦横710mm 、厚さ0.6mm の平滑表面を有するガラス状
炭素系のセパレータを準備した。ついで、セパレータの
互いに直交する表面と裏面の各幅45mmの端部をショット
ブラストして表1に示す表面粗さおよび薄肉度になるよ
うに粗面化と薄肉化を同時におこなった。
Hereinafter, examples of the present invention will be described in comparison with comparative examples. Examples 1 to 7 and Comparative Examples 1 to 9 Fine powder of graphite having an average particle size of 7 μm was added to a phenol resin, kneaded, roll-formed, calcined at a temperature of 1300 ° C., and carbonized at a temperature of 1300 ° C. and a thickness of 0.6 mm. Was prepared. Then, the 45 mm-wide end portions of the front surface and the back surface of the separator, which are orthogonal to each other, were shot blasted to simultaneously perform the surface roughening and the thinning so as to obtain the surface roughness and the thinness shown in Table 1.

【0018】接着剤としては、表1に示す成分組成 (黒
鉛微粉 100重量部当たりの配合重量部) の混練物を用い
た。、なお、芳香族ポリイミド前駆体は、無水ピロメリ
ト酸〔関東化学(株)製、試薬特級〕と4,4′ジアミ
ノジフェニルエーテル〔東京加成(株)製、試薬特級〕
をN,Nジメチルアセトアミド〔関東化学(株)製、試
薬特級〕中で重合して得た樹脂分20%のものを用いた。
また、フェノール樹脂初期縮合物は、市販品〔住友デュ
レズ(株)製、PR940 〕を使用した。
As the adhesive, a kneaded material having the component composition shown in Table 1 (mixed parts by weight per 100 parts by weight of graphite fine powder) was used. The aromatic polyimide precursor is pyromellitic anhydride [Kanto Chemical Co., Ltd., special grade reagent] and 4,4 'diaminodiphenyl ether [Tokyo Kasei Co., Ltd., special grade reagent]
Was polymerized in N, N dimethylacetamide [Kanto Chemical Co., Ltd., special grade reagent], and a resin content of 20% was used.
As the phenol resin precondensate, a commercially available product [PR940, manufactured by Sumitomo Durez Co., Ltd.] was used.

【0019】[0019]

【表1】 〈表注〉 (1)ポリイミド前駆体 (2)フェノール樹脂初
期縮合物
[Table 1] <Table notes> (1) Polyimide precursor (2) Phenolic resin precondensate

【0020】表1に示した接合部位に各同欄の組成を有
する接着剤を刷毛塗りにより均一に塗布したのち、接合
部位に端部シール材を重ねて圧力1kg/cm2、温度200 ℃
の条件で熱圧・硬化した。このようにして一体に接合し
た複合部材を機械加工し、一変の長さが700mm の正方形
で、端部シール材の厚さが2.4mm になる寸法に仕上げ
た。なお、各例のうち実施例7については、接合部位に
ポリテトラフルオロエチレンのディスパージョン〔旭硝
子(株)製、AD-1〕を塗布し、100 ℃で乾燥したのち34
0 ℃の温度で硬化処理をおこなった。
After the adhesive having the composition shown in the same column was uniformly applied to the joints shown in Table 1 by brushing, an end seal material was overlaid on the joints, and the pressure was 1 kg / cm 2 and the temperature was 200 ° C.
Heat-pressed and cured under the following conditions. The composite member integrally joined in this way was machined and finished to a dimension of a square having a variable length of 700 mm and a thickness of the end sealing material of 2.4 mm. In Example 7, of each example, a polytetrafluoroethylene dispersion [AD-1 manufactured by Asahi Glass Co., Ltd.] was applied to the joint, dried at 100 ° C., and then dried.
Curing was performed at a temperature of 0 ° C.

【0021】得られた各端部シール付燃料電池セパレー
タにつき、接合部の気体透過度(気密性)、加工歩留
り、ヒートサイクルテストおよびリン酸(200℃) 浸漬テ
スト等の測定をおこない、その結果を表2に示した。な
お、気体透過度は室温で1kg/cm2の窒素ガスでおこな
い、またヒートサイクルテストは250 ℃に保持された恒
温槽中に接合部材を入れ、取り出して室温に戻す操作を
1回とした。
With respect to each of the obtained fuel cell separators with end seals, the gas permeability (airtightness) of the joints, the processing yield, the heat cycle test, the phosphoric acid (200 ° C.) immersion test, and the like were measured. Are shown in Table 2. The gas permeability was measured at room temperature with 1 kg / cm 2 of nitrogen gas. In the heat cycle test, the operation of putting the joining member in a thermostat kept at 250 ° C., taking it out, and returning it to room temperature was performed once.

【0022】表2の結果から、比較例では気密性、加工
歩留り、耐ヒートサイクル性または耐蝕性のいずれかの
性能で欠陥が認められるが、本発明の要件を満たす実施
例では全ての特性において優れていることが判明する。
From the results shown in Table 2, defects are observed in any of the airtightness, processing yield, heat cycle resistance, and corrosion resistance in the comparative example. However, in the examples satisfying the requirements of the present invention, defects were observed in all characteristics. It turns out to be excellent.

【0023】[0023]

【表2】 [Table 2]

【0024】比較例10 熱膨張係数1×10-6-1のガラス状炭素系からなるセパ
レータと熱膨張係数2×10-6-1のカーボン材からなる
端部シール材を用い、実施例1と同一の条件およびプロ
セスで接合して複合部材を作製した。この異種材質を接
合した端部シール付燃料電池セパレータの各種性能を測
定したところ、気体透過度は10-6cc/cm2min 、加工歩留
りは90%と良好な結果であったが、ヒートサイクルテス
トでは5回で剥離現象が認められた。
[0024] Using the end seal member made of carbon material of Comparative Example 10 the thermal expansion coefficient of 1 × consists of glassy carbon of 10 -6 ° C. -1 separator and thermal expansion coefficient of 2 × 10 -6-1, performed A composite member was produced by joining under the same conditions and process as in Example 1. When the various performances of the fuel cell separator with the end seal bonded to the different materials were measured, the gas permeability was 10 −6 cc / cm 2 min and the processing yield was 90%, which was a good result. In the test, a peeling phenomenon was observed five times.

【0025】比較例11 実施例1と同一のセパレータと端部シール材を、セパレ
ータの接合部位になんらの加工を施すことなしに厚さ0.
05mmのポリテトラフルオロエチレンシート〔ニチアス
(株)製〕を介在させ、温度340 ℃、圧力10kg/cm2の熱
圧条件で接合した。この端部シール付燃料電池セパレー
タについて各種性能を測定したところ、気体透過度は10
-6cc/cm2min と良好な気密性を示したが、加工歩留りは
40%でヒートサイクルテストでは38回で剥離現象が発生
した。
COMPARATIVE EXAMPLE 11 The same separator and end seal material as in Example 1 were used to obtain a thickness of about 0.1 without any processing at the junction of the separator.
Bonding was performed under a hot and pressure condition of a temperature of 340 ° C. and a pressure of 10 kg / cm 2 with a 05 mm polytetrafluoroethylene sheet (manufactured by Nichias Corporation) interposed. When various performances of the fuel cell separator with the end seal were measured, the gas permeability was 10%.
It showed good airtightness of -6 cc / cm 2 min, but the processing yield was
At a heat cycle test of 40%, the peeling phenomenon occurred 38 times.

【0026】[0026]

【発明の効果】以上のとおり、本発明によれば簡便な手
段により気密性、耐ヒートサイクル性および耐蝕性に優
れた端部シール付燃料電池セパレータを加工歩留りよく
製造することができる。したがって、長期に運転に耐え
る高性能セルを効率的に生産供給することが可能となる
ほか、製造コストの低減化にも有効である。
As described above, according to the present invention, a fuel cell separator with an end seal excellent in airtightness, heat cycle resistance and corrosion resistance can be manufactured by a simple means with good processing yield. Therefore, it is possible to efficiently produce and supply high-performance cells that can withstand long-term operation, and it is also effective in reducing manufacturing costs.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 ガラス状炭素系セパレータの互いに直交
する表面と裏面の端部に、表面粗さが10μm Rz以上で
5〜300 μm 薄く形成した接合部位を設け、該接合部位
にセパレータと同材質の端部シール材を平均粒径70μm
以下のカーボン粉末 100重量部、芳香族ポリイミド前駆
体 100〜200 重量部およびフェノール樹脂初期縮合物20
〜50重量部からなる組成の接着剤を用いて接合し、熱圧
・硬化させることを特徴とする端部シール付燃料電池セ
パレータの製造方法。
1. A joining portion having a surface roughness of not less than 10 μm Rz and a thickness of 5 to 300 μm is provided at an end portion of a front surface and a back surface of a glassy carbon-based separator which are orthogonal to each other. 70μm average particle size
The following carbon powder 100 parts by weight, aromatic polyimide precursor 100 to 200 parts by weight and phenol resin precondensate 20
A method for producing a fuel cell separator with end seals, comprising joining with an adhesive having a composition of 50 to 50 parts by weight, followed by heat-pressure and curing.
JP07225091A 1991-03-11 1991-03-11 Method for manufacturing fuel cell separator with end seal Expired - Fee Related JP3240062B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP07225091A JP3240062B2 (en) 1991-03-11 1991-03-11 Method for manufacturing fuel cell separator with end seal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP07225091A JP3240062B2 (en) 1991-03-11 1991-03-11 Method for manufacturing fuel cell separator with end seal

Publications (2)

Publication Number Publication Date
JPH04282565A JPH04282565A (en) 1992-10-07
JP3240062B2 true JP3240062B2 (en) 2001-12-17

Family

ID=13483865

Family Applications (1)

Application Number Title Priority Date Filing Date
JP07225091A Expired - Fee Related JP3240062B2 (en) 1991-03-11 1991-03-11 Method for manufacturing fuel cell separator with end seal

Country Status (1)

Country Link
JP (1) JP3240062B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11297338A (en) * 1998-04-10 1999-10-29 Nisshinbo Ind Inc Separator for solid polymer type fuel cell, and manufacture thereof

Also Published As

Publication number Publication date
JPH04282565A (en) 1992-10-07

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