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JP2004071456A - Porous conductive plate - Google Patents

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Publication number
JP2004071456A
JP2004071456A JP2002231462A JP2002231462A JP2004071456A JP 2004071456 A JP2004071456 A JP 2004071456A JP 2002231462 A JP2002231462 A JP 2002231462A JP 2002231462 A JP2002231462 A JP 2002231462A JP 2004071456 A JP2004071456 A JP 2004071456A
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electrode assembly
conductive plate
membrane electrode
porous conductive
contact
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JP4346874B2 (en
Inventor
Takashi Onishi
大西 隆
Tadashi Ogasawara
小笠原 忠司
Masamichi Kato
加藤 雅通
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Osaka Titanium Technologies Co Ltd
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Osaka Titanium Technologies Co Ltd
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    • 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

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  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

【課題】固体高分子型水電解槽の給電体又は固体高分子型燃料電池の集電体として使用される多孔質導電板の成形性を高める。表面を平滑化し、膜電極接合体との接触性を高める。膜電極接合体が損傷する危険性を小さくする。
【解決手段】球状ガスアトマイズチタン粉末を焼結容器に充填し、真空焼結して、多孔質導電板となす。その導電板の表面を研削加工又は切削加工により平滑化する。
【選択図】   図4
An object of the present invention is to improve the formability of a porous conductive plate used as a power supply for a polymer electrolyte water electrolysis tank or a current collector for a polymer electrolyte fuel cell. Smooths the surface and enhances contact with the membrane electrode assembly. Reduce the risk of damaging the membrane electrode assembly.
A sintering container is filled with a spherical gas atomized titanium powder and vacuum-sintered to form a porous conductive plate. The surface of the conductive plate is smoothed by grinding or cutting.
[Selection diagram] Fig. 4

Description

【0001】
【発明の属する技術分野】
本発明は、固体高分子型水電解槽における給電体又は固体高分子型燃料電池における集電体として使用される多孔質導電板に関し、特に、チタン焼結体からなる多孔質導電板に関する。
【0002】
【従来の技術】
高分子電解質膜を用いて水素及び酸素を製造する水電解セルは、いわゆるフィルタープレス型に構成されている。具体的に説明すると、高分子電解質膜の両面に触媒層を接合して構成された膜電極接合体の両面側に給電体を配置してユニットを構成し、このユニットを多数積層して、その両端側に電極を設けた構成が一般に採用されている。
【0003】
ここにおける給電体は、多孔質の導電板からなり、隣接する膜電極接合体に密に接して配置される。給電体として多孔質の導電板を使用するのは、電流を通す必要があること、水電解反応のために水を供給する必要があること、水電解反応で生じたガスを速やかに排出する必要があることなどによる。
【0004】
また、高分子電解質膜を用いた燃料電池の構造も水電解槽のそれと全く同じであり、膜電極接合体の両面側には多孔質の導電板が配置されている。燃料電池の場合は、水素を燃料として電力を得ることから、この多孔質導電板は集電体と呼ばれている。
【0005】
このような固体高分子型水電解槽における給電体又は固体高分子型燃料電池における集電体として使用される多孔質導電板に関しては、酸化性雰囲気で使用できる特性も必要なため、カーボンと共にチタン材が検討されており、チタン材のなかでも特にチタン粉末焼結体が、表面が平滑で、隣接する膜電極接合体を損傷させ難いことや、適正な空隙率を得やすいことなどから注目されている。
【0006】
そして、このようなチタン粉末焼結体からなる多孔質導電板の一つとして、スポンジチタンを水素化脱水素により脆化し粉砕して得られたHDH粉末を圧縮後に焼結(CIP)し、製造されたチタン粉末焼結体を更にスライス加工することにより、表面が平滑なチタン粉末焼結板を製造する技術が、特開2000−328279号公報に記載されている。
【0007】
【発明が解決しようとする課題】
特開2000−328279号公報に記載されているチタン粉末焼結体では、表面がスライス加工により平滑化されているために、膜電極接合体との接触面積比率を高めることが可能になり、加えて、その表面の凹凸などに起因する膜電極接合体の破損を軽減することも可能になる。
【0008】
しかしながら、スポンジチタンの破砕粒子或いはスポンジチタンの水素化脱水素による脆化破砕粒子を原料とするチタン粉末焼結体では、原料粒子が角張った不定形状であるため、表面が平坦化されていても、膜電極接合体と各チタン粒子の接触面形状が円形にならず、鋭角な角部をもつ不定形となる箇所が多く発生する。このため、依然として膜電極接合体を損傷させる危険性が高い。
【0009】
この問題点はCIPを無加圧焼結に変更しても解決されない。CIPを無加圧焼結に変更した場合は、焼結板の表面を研削しても膜電極接合体との接触性は十分に改善されない。
【0010】
これらに加え、従来のチタン粉末焼結体は、プレス成形性が悪く、割れやすいため、薄型で大面積のものを製造できないという制約もある。
【0011】
本発明の目的は、成形性に優れるのは勿論のこと、膜電極接合体との接触性に優れ、しかも膜電極接合体を損傷させる危険性が小さい多孔質導電板を提供することにある。
【0012】
【課題を解決するための手段】
上記目的を達成するために、本発明者らは、球状ガスアトマイズチタン粉末に注目した。球状ガスアトマイズチタン粉末とは、ガスアトマイズ法により製造されたチタン又はチタン合金の粉末であり、個々の粒子は、チタン又はチタン合金の溶融飛沫が飛散中に凝固してできたものであるから、表面が滑らかな球形をしている。また、粒径は例えば平均で100μm以下と非常に微細にできる。
【0013】
ちなみに、スポンジチタンの破砕や水素化脱水素により製造されたチタン粉末の粒子形状は不定形である。また、球状チタン粒子は回転電極法によっても製造可能であるが、得られる平均粒度は一般に400μm以上である。
【0014】
本発明者らは、このような特徴を有する球状ガスアトマイズチタン粉末を用いて、固体高分子型水電解槽における給電体や固体高分子型燃料電池における集電体を想定した焼結板を試験的に製造し、その特性等を評価した。その結果、以下のことが明らかになった。
【0015】
球状ガスアトマイズチタン粉末は流動性に優れ、焼結容器内に投入すると、加圧なしでも十分な密度に充填される。そして、これを焼結すると、▲1▼薄型大面積の場合も十分な機械的強度が確保される。▲2▼給電体や集電体として好ましい空隙率が、格別の操作なしで簡単に得られる。▲3▼表面の平滑性が元々良好な上に、研削又は切削などによる平滑化加工を行うと、隣接する膜電極接合体との接触性が著しく向上する。▲4▼そして、この場合の膜電極接合体と各粒子の接触面形状がほぼ円形となり、鋭角な角部をもつ不定形が存在しなくなるため、従来のチタン粉末焼結体を用いた場合と比較して膜電極接合体の損傷を大幅に減らすことが可能になる。
【0016】
即ち、球状ガスアトマイズチタン粉末を用いた焼結体は、製造過程で加圧さえも行わず、また製造後に表面コートを行わずとも、表面の平滑化加工を行うだけで、固体高分子型水電解槽における給電体又は固体高分子型燃料電池における集電体として、性能及び経済性の両面から極めて優れた適性を示すものとなる。
【0017】
本発明の多孔質導電板は、かかる知見に基づいて開発されたもので、固体高分子型水電解槽における給電体又は固体高分子型燃料電池における集電体として使用される多孔質導電板であって、球状チタン粒子を原料とする空隙率が30〜50%の焼結体からなり、膜電極接合体に接触する面が平滑化されるように、その面の表層に位置する球状チタン粒子の表面側の一部分が、同一平面上に位置する平坦面とされたものである。
【0018】
前記平滑化は、研削加工又は切削加工により簡単に行うことができる。膜電極接合体に接触する面における接触面積比率は50〜80%が好ましい。この面積比率が50%未満の場合は表面の平滑化によっても接触性の改善が図れない。80%を超える場合は純水などの流体の供給が不十分となり、反応性が阻害される。特に好ましい面積比率は60〜70%である。ちなみに、前記平滑化が行われない場合の面積比率は40%以下である。
【0019】
本発明の多孔質導電板においては、原料粒子に球状チタン粒子を使用すること、及び焼結板の表面を平滑化することが重要であるが、これらと共に焼結体の空隙率も重要である。すなわち、球状チタン粒子を使用した焼結体であれば何でもよいというわけではなく、空隙率が30〜50%のものが必要である。空隙率が30%未満では流体の流通が不十分となるため、膜電極接合体近傍で発生するガスが焼結体を通って反対側へ流通することが困難になり、その結果、膜電極接合体の冷却不良による寿命短縮等が問題になる。分級などにより粒径をある程度そろえた球状チタン粒子を無加圧で焼結したときの空隙率は30〜50%程度になる。バインダを多量に加えるなどすれば球状チタン粒子を使用しても空隙率が50%を超えるものを製造できるが、空隙率が50%を超えると表面を平滑化しても膜電極接合体との接触性が不足する。加えて、焼結体内に粒子が「粗」の部分が多数生じるため、電気伝導度や発生ガスの排出能力などに面内不均一が発生することも問題になる。
【0020】
球状チタン粒子としては、粒径が小さい球状ガスアトマイズチタン粉末が好ましいが、回転電極法による球状チタン粒子の使用も可能である。球状ガスアトマイズチタン粉末としては、例えば粒径範囲によって区分された次の3種類が市販されている。即ち、45μm以下の細粒、45〜150μmの粗粒、更に粗い150μm以上の3種類であり、平均粒径は細粒で約25μm、粗粒で約80μmである。
【0021】
本発明の多孔質導電板に使用される球状ガスアトマイズチタン粉末の粒径は、特に限定せず、上述の市販品レベルで何ら問題はないが、ガスアトマイズ法と言えども極端な細粒を歩留りよく工業的に生産することは困難である。また、粗粒の場合は、薄型の多孔質体を製造した場合に多孔質体の厚みに対するチタン粉末間の接触点数が少なくなるために強度不足が懸念される。よって、粒径は平均で10〜150μmが好ましい。
【0022】
多孔質導電板の空隙率は、焼結温度の調節、粒径の選択、加圧等により制御可能である。一般的な傾向として、焼結温度が高くなると、接触面積が増大することから、空隙率が低下する。同様に、粒径が小さくなった場合も、接触面積が増大することから、空隙率が低下する傾向となる。また、充填時や焼結時に加圧を行えば、空隙率は低下する。また、多孔質導電板の板厚に対して粒径が大きくなると、空隙率が増大する傾向となる。これらの組み合わせにより、空隙率は比較的広い範囲で任意に制御される。なお、空隙率の極端な低減や増大は、反応における水やガスの受給効率の悪化や多孔質導電板の強度不足の原因になる。
【0023】
多孔質導電板の寸法は、製造される給電体や集電体の寸法に応じて適宜選択される。
【0024】
【発明の実施の形態】
以下、図面を参照して本発明の実施形態を説明する。図1〜図3は球状ガスアトマイズ粉末の充填形態を示す断面図である。
【0025】
まず、図1に示すように、所定粒径の球状ガスアトマイズチタン粉末1を高密度アルミナ製の焼結容器2に無加圧で充填する。焼結容器2の内形は、製造すべき多孔質導電板よりやや厚い薄板形状である。次いで、焼結容器2内に充填された球状ガスアトマイズチタン粉末1を無加圧で真空焼結する。
【0026】
焼結温度は、チタンの融点よりはるかに低い800〜1300℃が好ましい。焼結温度が800℃未満の場合は、十分な焼結が行われない。1300℃を超えると、無加圧の場合でも、焼結部分が個々の粒子同士の接触部にとどまらず、粒子同士が溶け合うため、適正な空隙率を確保できなくなるおそれがある。
【0027】
こうして製造された板状のチタン粉末焼結体の一方の表面(膜電極接合体に接触する面)を研削加工又は切削加工により平坦化する(図4参照)。他方の表面も合わせて平坦化すれば電解電圧が更に低下し、エネルギー効率が向上する。
【0028】
このような方法で300mm角×1mm厚の多孔質導電板を、本発明の実施例として製造した。使用した球状ガスアトマイズチタン粉末は、前述した市販品であり、粗粒(粒径範囲45〜150μm,平均粒径80μm)と細粒(粒径範囲45μm以下,平均粒径25μm)の2種類である。真空焼結での真空度は7×10−3Paとした。また、焼結温度は粗粒に対しては約1100℃(実施例1)と約1300℃(実施例3)、細粒に対しては約800℃(実施例2)と約900℃(実施例4)の各2種類とした。即ち、粗粒及び細粒のそれぞれについて焼結温度を変化させることにより、空隙率を2段階に調節した。平坦化は、焼結体の両面に対して研削加工により実施した。
【0029】
比較例として、研削加工を省略した。また、空隙率を30%未満の16%とした。また、原料粒子として、球状ガスアトマイズチタン粉末の代わりに、スポンジチタンを水素化脱水素により脆化し粉砕して得られたHDH粉末を使用した。そのHDH粉末に対してCIPと無加圧焼結を実施した。
【0030】
製造された各種の多孔質導電板について、膜電極接合体に対する接触性を、接触面積比率により評価した。接触面積比率は、各焼結体の接触面積を感圧フィルム(商品名プレスケール 富士フィルム製)により測定し、これを焼結体の面積で除することにより求めた。このときの測定圧力は1.47MPaとした。
【0031】
また、損失電圧を次の方法により測定した。焼結体を2枚の銅板で挟み、1.47MPaの圧力で加圧した状態で、1A/cm2 の直流電流を2枚の銅板間に通じ、その際の2枚の銅板間の電圧を測定した。
【0032】
更に、膜電極接合体への機械的影響を、前記感圧フィルムにおけるピンホールの有無により評価した。前記感圧フィルムの厚さは0.1mm、加圧力は前記のとおり1.47MPaである。
【0033】
結果を表1に示す。
【0034】
【表1】

Figure 2004071456
【0035】
比較例4は、HDH粉末にCIPを実施して製造した従来の焼結体である。表面を研削したため、膜電極接合体との接触性は良好である。しかし、膜電極接合体と各粒子の接触面形状が、鋭角な角部をもつ不定形となるため、膜電極接合体を損傷させる危険性は高い。比較例5は、HDH粉末を無加圧焼結して得た焼結体である。依然として膜電極接合体を損傷させる危険性が高い上に、膜電極接合体との接触性が低下した。
【0036】
比較例1,2は、球状ガスアトマイズチタン粉末を使用するものの、表面の切削加工を行わなかった焼結体である。膜電極接合体を損傷させる危険性は低く、空隙率も適正なるものの、膜電極接合体との接触性は不良である。
【0037】
実施例1〜4は、球状ガスアトマイズチタン粉末を使用した上で、表面の切削加工を行った焼結体である。実施例1で得た焼結体の断面形状を図4に研削加工前及び研削加工後について示す。表面の研削加工により、表面近傍に位置する球状チタン粒子の表面側の一部分が、同一平面上に位置する平坦面となっており、表面が非常に平滑である。このため、膜電極接合体との接触性が良好である。加えて、膜電極接合体と各粒子の接触面形状がほぼ円形となり、鋭角な角部をもつ不定形が存在しなくなるため、膜電極接合体を損傷させる危険性が著しく低下する。更には空隙率も適正である。そして原料粒径が小さいほど、膜電極接合体との接触性は向上する。
【0038】
比較例3は、球状ガスアトマイズチタン粉末を使用した上で、表面の切削加工を行ったものの、焼結温度の高温化により空隙率が過度に低下した焼結体である。膜電極接合体を損傷させる危険性が低く、膜電極接合体との接触性も良好であるが、流体の流通が不十分となることによる膜電極接合体の冷却不良、これによる寿命短縮が問題になる。
【0039】
焼結体表面の平滑性を更に高める方法としては、例えば、球状ガスアトマイズチタン粉末を、振動を付与しながら必要寸法の焼結容器に充填する方法がある。この振動充填によると、図2に示すように、焼結容器2の底部上面に接する表面だけでなく、開口側の表面の平滑性が向上し、空隙率の更なる均一化も図られる。また、図3に示すように、焼結容器2を、内側の板状空間が縦向きとなるように構成するのも有効である。内側の板状空間が縦向きになると、充填された球状ガスアトマイズチタン粉末1が両側の側面から自重による板厚方向の荷重を受け、両表面の平滑性が向上する。いずれの方法でも、充填率が増大することによる空隙率の低減を伴い、両者を併用することも可能である。
【0040】
成形方法としては、自然充填・真空焼結の他、球状ガスアトマイズチタン粉末をバインダに混練したものを、ドクターブレード法、射出成形法、押し出し法等でグリーン体を成形し、その後、バインダを除去して焼結してもよい。焼結後の多孔質導電板を圧延したり、グリーン体を圧延して表面の更なる平滑化や空隙率の調整を行うことも可能である。また、球状ガスアトマイズチタン粉末の粒度分布を小さくすることも表面の平滑化に有効である。
【0041】
【発明の効果】
以上に説明したとおり、本発明の多孔質導電板は、球状チタン粉末の焼結体により構成されることにより、成形性に優れるので、薄型大面積の製品を簡単に製造できる。表面の平滑化により、膜電極接合体との接触性に著しく優れるものとりなり、膜電極接合体を損傷させる危険性も小さい。
【図面の簡単な説明】
【図1】球状ガスアトマイズ粉末の充填形態の1例を示す断面図である。
【図2】球状ガスアトマイズ粉末の充填形態の他の例を示す断面図である。
【図3】球状ガスアトマイズ粉末の充填形態の更に他の例を示す断面図である。
【図4】本発明の実施例で得た焼結体の粒子構造を、研削加工前及び研削加工後について示す断面図である。
【符号の説明】
1 球状ガスアトマイズチタン粉末
2 焼結容器[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention relates to a porous conductive plate used as a power feeder in a polymer electrolyte water electrolyzer or a current collector in a polymer electrolyte fuel cell, and more particularly to a porous conductive plate made of a titanium sintered body.
[0002]
[Prior art]
A water electrolysis cell for producing hydrogen and oxygen using a polymer electrolyte membrane is configured as a so-called filter press type. More specifically, a unit is configured by arranging a power supply on both sides of a membrane electrode assembly configured by bonding catalyst layers on both sides of a polymer electrolyte membrane, and a large number of units are stacked. A configuration in which electrodes are provided at both ends is generally adopted.
[0003]
The power feeder here is made of a porous conductive plate, and is arranged in close contact with an adjacent membrane electrode assembly. The use of a porous conductive plate as a power feeder requires that an electric current be passed, that water must be supplied for the water electrolysis reaction, and that the gas generated by the water electrolysis reaction must be quickly discharged. It depends.
[0004]
The structure of a fuel cell using a polymer electrolyte membrane is exactly the same as that of a water electrolysis tank, and a porous conductive plate is disposed on both sides of the membrane electrode assembly. In the case of a fuel cell, electric power is obtained using hydrogen as fuel, and thus the porous conductive plate is called a current collector.
[0005]
As for the porous conductive plate used as a power supply in such a polymer electrolyte water electrolyzer or a current collector in a polymer electrolyte fuel cell, it is necessary to have a property that can be used in an oxidizing atmosphere. Materials are being studied, and among titanium materials, titanium powder sintered compacts in particular are attracting attention because they have a smooth surface and are unlikely to damage adjacent membrane electrode assemblies, and it is easy to obtain an appropriate porosity. ing.
[0006]
Then, as one of the porous conductive plates made of such a titanium powder sintered body, HDH powder obtained by embrittlement and grinding of sponge titanium by hydrodehydrogenation is compressed, then sintered (CIP) and manufactured. Japanese Patent Application Laid-Open No. 2000-328279 describes a technique for producing a titanium powder sintered plate having a smooth surface by further slicing the obtained titanium powder sintered body.
[0007]
[Problems to be solved by the invention]
In the titanium powder sintered body described in JP-A-2000-328279, since the surface is smoothed by slicing, the contact area ratio with the membrane electrode assembly can be increased. Thus, it is also possible to reduce damage to the membrane / electrode assembly due to irregularities on the surface.
[0008]
However, in the case of a titanium powder sintered body using crushed particles of sponge titanium or crushed particles embrittled by hydrodehydrogenation of sponge titanium as raw materials, the raw material particles have an angular and irregular shape, so even if the surface is flattened. In addition, the shape of the contact surface between the membrane electrode assembly and each titanium particle is not circular, and many irregular-shaped portions having sharp corners are generated. Therefore, there is still a high risk of damaging the membrane electrode assembly.
[0009]
This problem cannot be solved even if CIP is changed to pressureless sintering. When CIP is changed to pressureless sintering, even if the surface of the sintered plate is ground, the contact with the membrane electrode assembly is not sufficiently improved.
[0010]
In addition to these, the conventional titanium powder sintered body is inferior in press formability and is easily cracked, so that there is a restriction that a thin and large-area one cannot be manufactured.
[0011]
An object of the present invention is to provide a porous conductive plate which is excellent not only in formability but also excellent in contact with a membrane electrode assembly and has a low risk of damaging the membrane electrode assembly.
[0012]
[Means for Solving the Problems]
In order to achieve the above object, the present inventors have focused on spherical gas atomized titanium powder. Spherical gas atomized titanium powder is a powder of titanium or a titanium alloy produced by a gas atomization method, and individual particles are formed by solidification of molten droplets of titanium or a titanium alloy during scattering. It has a smooth spherical shape. In addition, the particle size can be very fine, for example, 100 μm or less on average.
[0013]
Incidentally, the particle shape of titanium powder produced by crushing or hydrodehydrogenation of titanium sponge is irregular. Spherical titanium particles can also be produced by a rotating electrode method, but the average particle size obtained is generally 400 μm or more.
[0014]
Using a spherical gas atomized titanium powder having such characteristics, the present inventors experimentally produced a sintered plate assuming a power supply in a polymer electrolyte water electrolysis tank and a current collector in a polymer electrolyte fuel cell. And evaluated its characteristics and the like. As a result, the following became clear.
[0015]
Spherical gas atomized titanium powder has excellent fluidity, and when charged into a sintering vessel, is filled to a sufficient density without pressure. When this is sintered, (1) sufficient mechanical strength is ensured even in the case of a thin and large area. {Circle over (2)} A porosity preferable as a power supply or a current collector can be easily obtained without any special operation. {Circle around (3)} When the smoothness of the surface is originally good and a smoothing process such as grinding or cutting is performed, the contact with the adjacent membrane electrode assembly is remarkably improved. (4) In this case, the shape of the contact surface between the membrane electrode assembly and each particle becomes substantially circular, and there is no irregular shape having sharp corners. In comparison, damage to the membrane electrode assembly can be significantly reduced.
[0016]
In other words, the sintered body using the spherical gas-atomized titanium powder does not need to be pressurized in the manufacturing process, and even if it is not subjected to surface coating after the manufacturing, the surface is smoothed only by the solid polymer type water electrolysis. As a power feeder in a tank or a current collector in a polymer electrolyte fuel cell, it exhibits extremely excellent suitability in terms of both performance and economy.
[0017]
The porous conductive plate of the present invention has been developed based on such knowledge, and is a porous conductive plate used as a power feeder in a polymer electrolyte water electrolysis tank or a current collector in a polymer electrolyte fuel cell. The spherical titanium particles are formed of a sintered body having a porosity of 30 to 50%, and the spherical titanium particles are located on the surface of the surface so that the surface in contact with the membrane electrode assembly is smoothed. Is a flat surface located on the same plane.
[0018]
The smoothing can be easily performed by grinding or cutting. The contact area ratio on the surface in contact with the membrane electrode assembly is preferably 50 to 80%. If the area ratio is less than 50%, the contactability cannot be improved even by smoothing the surface. If it exceeds 80%, the supply of fluid such as pure water becomes insufficient, and the reactivity is impaired. A particularly preferred area ratio is 60 to 70%. Incidentally, the area ratio when the smoothing is not performed is 40% or less.
[0019]
In the porous conductive plate of the present invention, it is important to use spherical titanium particles as the raw material particles and to smooth the surface of the sintered plate, and together with these, the porosity of the sintered body is also important. . That is, any sintered body using spherical titanium particles is not necessarily required, and a porosity of 30 to 50% is required. If the porosity is less than 30%, the flow of the fluid becomes insufficient, and it becomes difficult for the gas generated in the vicinity of the membrane electrode assembly to flow to the opposite side through the sintered body. Problems such as shortening of service life due to poor cooling of the body may occur. The porosity when spherical titanium particles having a uniform particle diameter by classification or the like are sintered without pressure is about 30 to 50%. If a large amount of a binder is added, a porosity exceeding 50% can be produced even when spherical titanium particles are used, but if the porosity exceeds 50%, even if the surface is smoothed, contact with the membrane electrode assembly can be achieved. Lacks sex. In addition, since a large number of "coarse" particles are generated in the sintered body, in-plane non-uniformity in electric conductivity, ability to discharge generated gas, and the like also poses a problem.
[0020]
As the spherical titanium particles, spherical gas atomized titanium powder having a small particle diameter is preferable, but spherical titanium particles obtained by a rotating electrode method can also be used. As the spherical gas atomized titanium powder, for example, the following three types classified by particle size range are commercially available. That is, there are three types of fine particles of 45 μm or less, coarse particles of 45 to 150 μm, and further coarse particles of 150 μm or more. The average particle size is about 25 μm for fine particles and about 80 μm for coarse particles.
[0021]
The particle size of the spherical gas atomized titanium powder used for the porous conductive plate of the present invention is not particularly limited, and there is no problem at the level of the above-mentioned commercial products. Production is difficult. Further, in the case of coarse particles, when a thin porous body is manufactured, the number of contact points between titanium powders with respect to the thickness of the porous body is reduced, and thus there is a concern about insufficient strength. Therefore, the average particle size is preferably 10 to 150 μm.
[0022]
The porosity of the porous conductive plate can be controlled by adjusting the sintering temperature, selecting the particle size, and applying pressure. As a general tendency, as the sintering temperature increases, the porosity decreases because the contact area increases. Similarly, when the particle size is reduced, the porosity tends to decrease because the contact area increases. Also, if pressure is applied during filling or sintering, the porosity decreases. In addition, when the particle size increases with respect to the thickness of the porous conductive plate, the porosity tends to increase. By these combinations, the porosity is arbitrarily controlled in a relatively wide range. Note that an extreme decrease or increase in the porosity causes deterioration of the water or gas supply efficiency in the reaction and insufficient strength of the porous conductive plate.
[0023]
The dimensions of the porous conductive plate are appropriately selected according to the dimensions of the power supply and the current collector to be manufactured.
[0024]
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, embodiments of the present invention will be described with reference to the drawings. FIG. 1 to FIG. 3 are cross-sectional views showing a filling form of the spherical gas atomized powder.
[0025]
First, as shown in FIG. 1, a spherical gas atomized titanium powder 1 having a predetermined particle size is filled in a sintered container 2 made of high-density alumina without pressure. The inner shape of the sintering vessel 2 is a thin plate slightly thicker than the porous conductive plate to be manufactured. Next, the spherical gas atomized titanium powder 1 filled in the sintering container 2 is vacuum-sintered without pressure.
[0026]
The sintering temperature is preferably 800 to 1300 ° C., which is much lower than the melting point of titanium. When the sintering temperature is lower than 800 ° C., sufficient sintering is not performed. When the temperature exceeds 1300 ° C., even when no pressure is applied, the sintered portion does not remain at the contact portion between the individual particles, but the particles are fused with each other, so that an appropriate porosity may not be secured.
[0027]
One surface (the surface in contact with the membrane electrode assembly) of the plate-like titanium powder sintered body thus manufactured is flattened by grinding or cutting (see FIG. 4). If the other surface is also flattened, the electrolytic voltage is further reduced, and the energy efficiency is improved.
[0028]
In this way, a 300 mm square × 1 mm thick porous conductive plate was manufactured as an example of the present invention. The spherical gas atomized titanium powder used is the above-mentioned commercially available product, and is classified into coarse particles (particle size range: 45 to 150 μm, average particle size: 80 μm) and fine particles (particle size range: 45 μm or less, average particle size: 25 μm). . The degree of vacuum in vacuum sintering was 7 × 10 −3 Pa. The sintering temperature is about 1100 ° C. (Example 1) and about 1300 ° C. (Example 3) for coarse grains, and about 800 ° C. (Example 2) and about 900 ° C. (Example) for fine grains. Each of the two examples 4) was used. That is, the porosity was adjusted in two stages by changing the sintering temperature for each of the coarse particles and the fine particles. The flattening was performed by grinding both surfaces of the sintered body.
[0029]
As a comparative example, grinding was omitted. Further, the porosity was set to 16% which is less than 30%. In addition, instead of spherical gas atomized titanium powder, HDH powder obtained by emulsifying and pulverizing sponge titanium by hydrodehydrogenation was used as the raw material particles. CIP and pressureless sintering were performed on the HDH powder.
[0030]
For each of the manufactured porous conductive plates, the contact property with the membrane electrode assembly was evaluated based on the contact area ratio. The contact area ratio was determined by measuring the contact area of each sintered body with a pressure-sensitive film (trade name, manufactured by Prescale Fuji Film), and dividing this by the area of the sintered body. The measurement pressure at this time was 1.47 MPa.
[0031]
Further, the loss voltage was measured by the following method. With the sintered body sandwiched between two copper plates, a DC current of 1 A / cm 2 is passed between the two copper plates under a pressure of 1.47 MPa, and the voltage between the two copper plates at that time is reduced. It was measured.
[0032]
Further, the mechanical influence on the membrane electrode assembly was evaluated based on the presence or absence of pinholes in the pressure-sensitive film. The thickness of the pressure-sensitive film is 0.1 mm, and the pressing force is 1.47 MPa as described above.
[0033]
Table 1 shows the results.
[0034]
[Table 1]
Figure 2004071456
[0035]
Comparative Example 4 is a conventional sintered body manufactured by performing CIP on HDH powder. Since the surface is ground, the contact with the membrane electrode assembly is good. However, since the shape of the contact surface between the membrane electrode assembly and each particle is indefinite with sharp corners, there is a high risk of damaging the membrane electrode assembly. Comparative Example 5 is a sintered body obtained by sintering HDH powder under no pressure. There is still a high risk of damaging the membrane electrode assembly, and the contact with the membrane electrode assembly has been reduced.
[0036]
Comparative Examples 1 and 2 are sintered bodies using spherical gas-atomized titanium powder, but without cutting the surface. Although the risk of damaging the membrane electrode assembly is low and the porosity is appropriate, the contact with the membrane electrode assembly is poor.
[0037]
Examples 1 to 4 are sintered bodies obtained by cutting the surface after using spherical gas atomized titanium powder. FIG. 4 shows the cross-sectional shape of the sintered body obtained in Example 1 before and after grinding. Due to the surface grinding, a part of the surface side of the spherical titanium particles located near the surface becomes a flat surface located on the same plane, and the surface is very smooth. Therefore, the contact with the membrane electrode assembly is good. In addition, since the shape of the contact surface between the membrane electrode assembly and each particle becomes substantially circular and there is no irregular shape having sharp corners, the risk of damaging the membrane electrode assembly is significantly reduced. Furthermore, the porosity is also appropriate. And the smaller the raw material particle size, the better the contact with the membrane electrode assembly.
[0038]
Comparative Example 3 is a sintered body in which the porosity was excessively reduced due to an increase in the sintering temperature although the surface was cut after using the spherical gas atomized titanium powder. Low risk of damaging the membrane electrode assembly and good contact with the membrane electrode assembly, but insufficient cooling of the membrane electrode assembly due to inadequate fluid flow, resulting in shortened service life become.
[0039]
As a method of further improving the smoothness of the surface of the sintered body, for example, there is a method of filling spherical gas atomized titanium powder into a sintering vessel of required dimensions while applying vibration. According to this vibration filling, as shown in FIG. 2, not only the surface in contact with the upper surface of the bottom of the sintering vessel 2 but also the smoothness of the surface on the opening side is improved, and the porosity is further uniformed. As shown in FIG. 3, it is also effective to configure the sintering container 2 so that the inner plate-shaped space is oriented vertically. When the inner plate-like space is oriented vertically, the filled spherical gas atomized titanium powder 1 receives a load in the plate thickness direction by its own weight from both side surfaces, and the smoothness of both surfaces is improved. Either method involves a reduction in porosity due to an increase in the filling rate, and it is also possible to use both together.
[0040]
As a molding method, in addition to natural filling and vacuum sintering, a green body is formed by kneading a spherical gas atomized titanium powder into a binder by a doctor blade method, an injection molding method, an extrusion method, and then removing the binder. Sintering. The porous conductive plate after sintering can be rolled, or the green body can be rolled to further smooth the surface and adjust the porosity. Also, reducing the particle size distribution of the spherical gas atomized titanium powder is effective for smoothing the surface.
[0041]
【The invention's effect】
As described above, since the porous conductive plate of the present invention is formed of a sintered body of spherical titanium powder and has excellent moldability, a thin and large-area product can be easily manufactured. Due to the smoothing of the surface, the contact with the membrane electrode assembly is extremely excellent, and the risk of damaging the membrane electrode assembly is small.
[Brief description of the drawings]
FIG. 1 is a cross-sectional view showing an example of a filling form of a spherical gas atomized powder.
FIG. 2 is a cross-sectional view showing another example of a filling form of a spherical gas atomized powder.
FIG. 3 is a cross-sectional view showing still another example of a filling form of a spherical gas atomized powder.
FIG. 4 is a cross-sectional view showing a particle structure of a sintered body obtained in an example of the present invention before and after grinding.
[Explanation of symbols]
1 Spherical gas atomized titanium powder 2 Sintering vessel

Claims (3)

固体高分子型水電解槽における給電体又は固体高分子型燃料電池における集電体として使用される多孔質導電板であって、球状チタン粒子を原料とする空隙率が30〜50%の焼結体からなり、膜電極接合体に接触する面が平滑化されるように、その面の表層に位置する球状チタン粒子の表面側の一部分が、同一平面上に位置する平坦面とされていることを特徴とする多孔質導電板。A porous conductive plate used as a power feeder in a polymer electrolyte water electrolyzer or a current collector in a polymer electrolyte fuel cell, wherein the sintered body has a porosity of 30 to 50% using spherical titanium particles as a raw material. A part of the surface side of the spherical titanium particles located on the surface of the surface is a flat surface located on the same plane so that the surface in contact with the membrane electrode assembly is smoothed. A porous conductive plate, characterized in that: 膜電極接合体に接触する面の表層に位置する球状チタン粒子の表面側の一部分が、研削又は切削により、同一平面上に位置する平坦面とされていることを特徴とする請求項1に記載の多孔質導電板。The surface part of the spherical titanium particles located on the surface of the surface in contact with the membrane electrode assembly is formed into a flat surface located on the same plane by grinding or cutting. Porous conductive plate. 膜電極接合体に接触する面における接触面積比率が50〜80%であることを特徴とする請求項1又は2に記載の多孔質導電板。3. The porous conductive plate according to claim 1, wherein a contact area ratio of the surface in contact with the membrane electrode assembly is 50 to 80%. 4.
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