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JPS6046514B2 - Manufacturing method of battery air electrode - Google Patents

Manufacturing method of battery air electrode

Info

Publication number
JPS6046514B2
JPS6046514B2 JP53163293A JP16329378A JPS6046514B2 JP S6046514 B2 JPS6046514 B2 JP S6046514B2 JP 53163293 A JP53163293 A JP 53163293A JP 16329378 A JP16329378 A JP 16329378A JP S6046514 B2 JPS6046514 B2 JP S6046514B2
Authority
JP
Japan
Prior art keywords
graphite
activated carbon
air electrode
water repellent
adsorbed
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
Application number
JP53163293A
Other languages
Japanese (ja)
Other versions
JPS5588273A (en
Inventor
辰夫 菊池
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.)
Furukawa Battery Co Ltd
Original Assignee
Furukawa Battery 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 Furukawa Battery Co Ltd filed Critical Furukawa Battery Co Ltd
Priority to JP53163293A priority Critical patent/JPS6046514B2/en
Publication of JPS5588273A publication Critical patent/JPS5588273A/en
Publication of JPS6046514B2 publication Critical patent/JPS6046514B2/en
Expired legal-status Critical Current

Links

Classifications

    • 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

Landscapes

  • Inert Electrodes (AREA)

Description

【発明の詳細な説明】 本発明は金属−空気電池に用いる空気極の製造方法に
関し、とくに電解液として海中等の中性電解質のものを
用いた電池に好適な製造方法を得んとするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing an air electrode used in a metal-air battery, and particularly aims to provide a manufacturing method suitable for batteries using a neutral electrolyte such as marine electrolyte as the electrolyte. It is.

従来金属一空気電池に用いる空気極は、活性炭と黒鉛
とを混合して、これに四沸化エチレン樹脂からなる撥水
剤を含浸吸着させた後加圧成形することにより製造され
ている。このように活性炭と黒鉛とを混合するのは、活
性炭は活性度に優れているが強度が弱く、これを強度の
高い黒鉛で補強するようにしたためである。しかし活性
炭と黒鉛とは活性度や強度のみならす、撥水剤の吸着性
が異なり、これらの混合物に撥水剤を含浸吸着させると
、黒鉛に多く吸着されて活性炭にはあまり吸着されない
。このため電池使用時において活性炭か早く劣化して寿
命が短かくなる問題がある。 このようなことから従来
においては、撥水剤の量を多くして活性炭も撥水剤を十
分含浸吸着するようにしているが、このようにすると撥
水性が強すきて電圧の立ち上り等の極板特性か劣化し、
とくに海水等中性電解質の電解液を用いた場合にはこの
傾向が著しい。 本発明は上記事情に鑑みてなされたも
ので、その目的とするところは、中性電解質の電解液を
用いた場合においても極板性能に優れ、しかも空気極の
寿命を維持することができる電池空気極の製造方法を提
供するものてある。
Conventionally, air electrodes used in metal-air batteries have been manufactured by mixing activated carbon and graphite, impregnating and adsorbing a water repellent made of tetrafluoroethylene resin, and then press-molding the mixture. The reason why activated carbon and graphite are mixed in this way is that activated carbon has excellent activity but low strength, and this is reinforced with graphite, which has high strength. However, activated carbon and graphite differ not only in their activity and strength but also in their ability to adsorb water repellents, and when a mixture of these is impregnated with a water repellent and adsorbed, much of it is adsorbed by graphite and not much by activated carbon. Therefore, when the battery is used, the activated carbon deteriorates quickly, resulting in a shortened lifespan. For this reason, in the past, the amount of water repellent was increased so that the activated carbon could be sufficiently impregnated with and adsorbed, but this made the water repellent stronger and caused problems such as voltage rise. Board properties deteriorate,
This tendency is particularly noticeable when a neutral electrolyte solution such as seawater is used. The present invention has been made in view of the above circumstances, and its purpose is to provide a battery that has excellent electrode plate performance even when a neutral electrolyte is used, and that can maintain the life of the air electrode. A method for manufacturing an air electrode is provided.

すなわち本発明は活性炭及び黒鉛にそれぞれ別個に撥
水剤を合着吸着させてこれらを乾燥した後、該活性炭及
び黒鉛にバインダーを添加して混合粉砕し、ついでこれ
を基体に載せて所望形状に加圧成形する方法てある。
That is, in the present invention, a water repellent agent is separately adsorbed onto activated carbon and graphite, and after these are dried, a binder is added to the activated carbon and graphite, the mixture is pulverized, and then this is placed on a substrate and shaped into a desired shape. There is a method of pressure molding.

以下本発明方法を詳細に説明する。 The method of the present invention will be explained in detail below.

まず活性炭と黒鉛とにそれぞれ別個に四沸化エチレン
樹脂を分散せしめた撥水剤を含浸吸着させる。
First, activated carbon and graphite are impregnated and adsorbed with a water repellent in which tetrafluoroethylene resin is separately dispersed.

このように別個に撥水剤を含浸吸着させることにより、
黒鉛にのみ撥水剤が吸着されることなく、黒鉛及び活性
炭にそれぞれ適量の撥水剤が吸着される。この場合活性
炭、及び黒鉛に対して含浸せしめる撥水剤の量は、電極
寿命時間、極板特性、基体に対する接着性などを考慮し
て決められ、活性炭においては活性炭1卯重量部に対し
て撥水剤32〜7鍾量部、又黒鉛においては黒鉛100
重量部に対して撥水剤32〜50重量部が好適てある。
ついで撥水剤を含浸、吸着した活性炭及び黒鉛をそれ
ぞれ乾燥し、さらに焼成する。
By separately impregnating and adsorbing water repellent in this way,
The water repellent is not adsorbed only on the graphite, but appropriate amounts of the water repellent are adsorbed on each of the graphite and activated carbon. In this case, the amount of water repellent to be impregnated into the activated carbon and graphite is determined by taking into account electrode life time, electrode plate characteristics, adhesion to the substrate, etc. 32 to 7 parts of water, and 100 parts of graphite
It is preferable to use 32 to 50 parts by weight of the water repellent agent.
Next, the activated carbon and graphite impregnated with a water repellent and adsorbed thereon are dried, and then fired.

この乾燥は、例えば120℃て3時間程度行ない、又焼
成は300〜360℃で1時間程度行なう。さらに焼成
した活性炭及び黒鉛をバインダーとともに混合粉砕し、
これを第1図に示す基体1上に載せて所望形状に加圧成
形する。
This drying is carried out, for example, at 120°C for about 3 hours, and the baking is carried out at 300-360°C for about 1 hour. Furthermore, the fired activated carbon and graphite are mixed and crushed with a binder,
This is placed on a substrate 1 shown in FIG. 1 and pressure-molded into a desired shape.

ここで活性炭に対する黒鉛の量は、活性炭10唾量部に
対して黒鉛80重量部が好ましく、又バインダーとして
は例えは、四弗化エチレン樹脂(PTF′E)などを用
い、活性炭と黒鉛の総量10呼量部に対して10重量部
程度が好適てある。又基体1は亜鉛金網、銅金網、ニッ
ケル金網などの網状のもので、網目の大きさは活性炭と
黒鉛の密着性を考慮して50メッシュ程度のものが好ま
しい。さらに加圧におけるブレス圧は500k9/C!
l以上であればよい。このようにして得られた空気極は
、第1図に示すように金網からなる基体1に活性炭と黒
鉛とからなるカーボン極2を設けているが、活性炭及び
黒鉛はそれぞれ適量の撥水剤を吸着しているので、電圧
の立ち上り等の空気極特性に優れ、しかも寿命を長く維
持することができる。次に上述した製造方法を具体的に
おこなつて、その効果を確かめた。
Here, the amount of graphite relative to activated carbon is preferably 80 parts by weight of graphite per 10 parts of activated carbon, and as a binder, for example, polytetrafluoroethylene resin (PTF'E) is used, and the total amount of activated carbon and graphite is Approximately 10 parts by weight per 10 parts by weight is suitable. The substrate 1 is made of a mesh such as zinc wire mesh, copper wire mesh, nickel wire mesh, etc., and the mesh size is preferably about 50 mesh in consideration of the adhesion between activated carbon and graphite. Furthermore, the breath pressure during pressurization is 500k9/C!
It is sufficient if it is equal to or larger than l. As shown in Figure 1, the air electrode thus obtained has a carbon electrode 2 made of activated carbon and graphite on a base 1 made of wire mesh. Because it is adsorbed, it has excellent air electrode characteristics such as voltage rise, and can maintain a long service life. Next, the above-described manufacturing method was specifically carried out to confirm its effectiveness.

ます活性炭25yに四弗化エチレン樹脂を含む撥水剤1
2yを含浸吸着させ、又黒鉛25yに該撥水剤12yを
含浸吸着させ、これらをそれぞれ120℃て3時間乾燥
した後、300〜360℃て1時間焼成した。
Water repellent 1 containing activated carbon 25y and tetrafluoroethylene resin
2y was impregnated and adsorbed, and graphite 25y was impregnated and adsorbed with the water repellent 12y, and after drying at 120°C for 3 hours, they were fired at 300 to 360°C for 1 hour.

ついでこの活性炭と黒鉛とをバイングーとして四弗化エ
チレン樹脂(PTFE)10yとともに混合粉砕し、こ
れをニッケル金網製の基体上に載せて500k9/CI
Lのブレス圧で加圧成形した。このようにして得られた
空気極を、塩化第1水銀電極(HgCl2、カロメル電
極)を参照電極として海水中での電圧立ち上り特性を調
べた。その結果を第2図の曲線aに示す。これに対し、
活性炭25yと黒鉛25yとを混合し、この混合物に撥
水剤20yを含浸吸着させ、以下上記実施例と同様にし
て空気極を作製し、その.電圧立ち上り特性を調べた。
Next, this activated carbon and graphite were mixed and pulverized together with 10y of polytetrafluoroethylene resin (PTFE) as binggu, and this was placed on a base made of nickel wire mesh and 500k9/CI
Pressure molding was performed with a press pressure of L. The voltage rise characteristics of the thus obtained air electrode in seawater were investigated using a mercurous chloride electrode (HgCl2, calomel electrode) as a reference electrode. The results are shown in curve a of FIG. In contrast,
Activated carbon 25y and graphite 25y are mixed, water repellent 20y is impregnated and adsorbed into this mixture, and an air electrode is produced in the same manner as in the above example. The voltage rise characteristics were investigated.

その結果を第2図の曲線bで示す。なお本発明方法は上
記実施例に限らず、活性炭と黒鉛とをバインダーととも
に混合粉砕した後アルコール等で造粒を行なうようにし
てもよい。
The results are shown by curve b in FIG. Note that the method of the present invention is not limited to the above-mentioned embodiments; activated carbon and graphite may be mixed and ground together with a binder, and then granulated with alcohol or the like.

すなわち撥水剤を含浸、吸着した活性炭及び黒鉛を乾燥
、焼成した後、これらをバ・インターとともに混合粉砕
し、ついでこの混合粉末に、アルコール、アセトン、陽
イオン界面活性剤溶液等を噴霧し、あるいはこれらを混
合粉末とともに攪拌することにより造粒し、このように
して得られた粒状形カーボン粉末を基体上に載せて加圧
成形することにより空気極が作られる。この場合造粒剤
としてアルコールを用いた場合、例えば混合粉末201
に対してアルコール5〜20cc程度の割合が好ましく
、とくに15cc程度が好適てある。このようにアルコ
ール等の造粒剤を用いた場合には、ブレス時に粉末の飛
散が生じることがなく、ブレス操作が容易であるととも
にブレス成形を基体全面にわたつて行なうことができ、
極板の寿命、分極値などの極板特性を高めることができ
る。
That is, after drying and calcining the activated carbon and graphite that have been impregnated and adsorbed with a water repellent agent, they are mixed and ground with Ba-Inter, and then this mixed powder is sprayed with alcohol, acetone, a cationic surfactant solution, etc. Alternatively, an air electrode is produced by stirring these together with a mixed powder to granulate them, placing the thus obtained granular carbon powder on a substrate, and press-molding it. In this case, when alcohol is used as a granulating agent, for example, mixed powder 201
A ratio of approximately 5 to 20 cc of alcohol to the amount of alcohol is preferred, and a ratio of approximately 15 cc is particularly preferred. When a granulating agent such as alcohol is used in this way, there is no scattering of powder during pressing, and the pressing operation is easy, and pressing can be performed over the entire surface of the base.
It is possible to improve the plate properties such as the life of the plate and the polarization value.

以上説明したように本発明によれば、活性炭及び黒鉛を
別々に撥水処理してから混合するようにしたので、空気
極の極板特性に優れ、しかも長寿命化を図ることができ
、とくに海水等の中性電解質の電解液を用いた金属一空
気海水電池用空気極の製造方法としてきわめて有益てあ
る。
As explained above, according to the present invention, activated carbon and graphite are treated separately to make them water repellent and then mixed together, so that the air electrode has excellent properties and has a long service life. This method is extremely useful as a method for manufacturing air electrodes for metal-air-seawater batteries using a neutral electrolyte such as seawater.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明方法に係る空気極の断面図、第2図は同
空気極を用いた金属一空気電池の電圧立上り特性を従来
の電池の場合と比較して示した図てある。 1・・・・・・基体、2・・・・・幼一ボン極。
FIG. 1 is a sectional view of an air electrode according to the method of the present invention, and FIG. 2 is a diagram showing the voltage rise characteristics of a metal-air battery using the same air electrode in comparison with that of a conventional battery. 1...Base, 2...Yoichi Bon pole.

Claims (1)

【特許請求の範囲】[Claims] 1 活性炭及び黒鉛にそれぞれ別個に撥水剤を含浸吸着
させて、これらを乾燥した後、該活性炭及び黒鉛にバイ
ンダーを添加して混合粉砕し、ついでこれを基体上に載
せて所望形状に加圧成形することを特徴とする電池空気
極の製造方法。
1. Activated carbon and graphite are separately impregnated and adsorbed with a water repellent, and after drying these, a binder is added to the activated carbon and graphite, mixed and pulverized, and then placed on a substrate and pressurized into the desired shape. A method for manufacturing a battery air electrode, characterized by molding.
JP53163293A 1978-12-27 1978-12-27 Manufacturing method of battery air electrode Expired JPS6046514B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP53163293A JPS6046514B2 (en) 1978-12-27 1978-12-27 Manufacturing method of battery air electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP53163293A JPS6046514B2 (en) 1978-12-27 1978-12-27 Manufacturing method of battery air electrode

Publications (2)

Publication Number Publication Date
JPS5588273A JPS5588273A (en) 1980-07-03
JPS6046514B2 true JPS6046514B2 (en) 1985-10-16

Family

ID=15771065

Family Applications (1)

Application Number Title Priority Date Filing Date
JP53163293A Expired JPS6046514B2 (en) 1978-12-27 1978-12-27 Manufacturing method of battery air electrode

Country Status (1)

Country Link
JP (1) JPS6046514B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63180810U (en) * 1987-05-14 1988-11-22

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2773112B2 (en) * 1986-02-06 1998-07-09 東芝電池株式会社 Gas diffusion electrode
CN102468493B (en) * 2010-11-09 2014-03-12 中国科学院金属研究所 Preparation method of high-activity vanadium battery electrode material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63180810U (en) * 1987-05-14 1988-11-22

Also Published As

Publication number Publication date
JPS5588273A (en) 1980-07-03

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