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JPS593027B2 - Cathode for alkaline batteries - Google Patents
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JPS593027B2 - Cathode for alkaline batteries - Google Patents

Cathode for alkaline batteries

Info

Publication number
JPS593027B2
JPS593027B2 JP50013334A JP1333475A JPS593027B2 JP S593027 B2 JPS593027 B2 JP S593027B2 JP 50013334 A JP50013334 A JP 50013334A JP 1333475 A JP1333475 A JP 1333475A JP S593027 B2 JPS593027 B2 JP S593027B2
Authority
JP
Japan
Prior art keywords
cathode
active material
fibrous sheet
battery
alkaline
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
JP50013334A
Other languages
Japanese (ja)
Other versions
JPS5189133A (en
Inventor
博一 仁木
保 城上
和夫 相沢
勉 高村
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.)
Toshiba Corp
Original Assignee
Tokyo Shibaura Electric 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 Tokyo Shibaura Electric Co Ltd filed Critical Tokyo Shibaura Electric Co Ltd
Priority to JP50013334A priority Critical patent/JPS593027B2/en
Publication of JPS5189133A publication Critical patent/JPS5189133A/ja
Publication of JPS593027B2 publication Critical patent/JPS593027B2/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
    • Y02E60/10Energy storage using batteries

Landscapes

  • Battery Electrode And Active Subsutance (AREA)

Description

【発明の詳細な説明】 本発明は亜鉛などの陰極活物質を陰極集電体に。[Detailed description of the invention] The present invention uses a cathode active material such as zinc as a cathode current collector.

着設する構造のアルカリ蓄電池用陰極の製造方法に関す
る。アルカリ電池は、充放電できる2次電池として、た
とえば陰極活物質に亜鉛を、陽極活物質として酸化ニッ
ケルあるいは酸化銀などを用いて陰陽電極とし、苛性カ
リ溶液を電解液と1、て構成したものである。
The present invention relates to a method for manufacturing a cathode for an alkaline storage battery having a structure in which the cathode is attached. An alkaline battery is a secondary battery that can be charged and discharged, and is made up of negative and positive electrodes, such as zinc as the negative active material and nickel oxide or silver oxide as the positive active material, and a caustic potash solution as the electrolyte. be.

このアルカリ電池用陰極として従来用いられていたもの
としてポリビニルアルコール、ポリスチレン、ポリアク
リル酸塩などの結着剤で陰極活物質を粘着性混合物とし
て陰極集電体に塗着1−て構成していた。
The cathode conventionally used for alkaline batteries consists of a cathode active material applied as a sticky mixture to a cathode current collector using a binder such as polyvinyl alcohol, polystyrene, or polyacrylate. .

しかしながら、従来の結着剤を用いた陰極であつてはい
ずれもアルカリ電池として満足した性能が得られない。
However, with any cathode using a conventional binder, satisfactory performance as an alkaline battery cannot be obtained.

たとえば、ポリビニルアルコールを用いた場合には、濃
厚アルカリ液中で除々に劣化し集電体から活物質の脱落
を生じる。またポリスオレンを用いた場合には、その電
気抵抗が大きいために電池の内部抵抗を増大させること
になり、これを減少させるために混合割合を少なくする
と強度が充分に取れないなどの欠点があり実用上好まし
くない。さらにポリアクリル酸塩を用いた場合には、電
解液に溶解するために充放電を繰り返えすことにより電
極が変形し短絡を生じる原因となるなどいずれの結着剤
であつても多くの欠点を有しておリアルカリ電池用陰極
を構成するには不適当なものである。本発明は陰極活物
質と、フッ素樹脂の水性分散液と、耐アルカリ性短繊維
からなる混合物を展開して繊維状シート体を得た後、前
記繊維状シート体の展開方向が異る如く積層展開し、複
数層に積層された繊維状シート体を集電体に着設するこ
とにより、柔軟性に富み、長期の充放電サイクルに対し
て変形などを生じることなく、さらに耐アルカリ性電池
反応の効率が優れたアルカリ蓄電池用陰極を得ることの
できる製造方法を提供することを目的とする。
For example, when polyvinyl alcohol is used, it gradually deteriorates in a concentrated alkaline solution, causing the active material to fall off from the current collector. In addition, when polyolene is used, its high electrical resistance increases the internal resistance of the battery, and if the mixing ratio is reduced to reduce this, it has disadvantages such as insufficient strength. Not good. Furthermore, when polyacrylate is used, repeated charging and discharging to dissolve it in the electrolyte can deform the electrode and cause short circuits. It is unsuitable for constructing a cathode for a real alkaline battery. In the present invention, a mixture consisting of a cathode active material, an aqueous dispersion of a fluororesin, and alkali-resistant short fibers is developed to obtain a fibrous sheet body, and then the fibrous sheet body is laminated and developed so that the directions of the fibrous sheet bodies are different. However, by attaching multiple layers of fibrous sheets to the current collector, it is highly flexible and does not deform during long charge/discharge cycles, and it also improves the efficiency of alkali-resistant battery reactions. An object of the present invention is to provide a manufacturing method that allows a cathode for an alkaline storage battery with excellent properties to be obtained.

つまり本発明方法においては、短繊維を混入することお
よび、フッ素樹脂の水性分散液を混練展開し、展開方向
が異なる如く積層化することの相乗効果により、複雑に
交錯1,た繊維状シート体が得られ柔軟性及び機械的強
度が著12く向上する。
In other words, in the method of the present invention, due to the synergistic effect of mixing short fibers, kneading and spreading an aqueous fluororesin dispersion, and laminating them in different directions of spreading, a fibrous sheet with intricately interwoven structures is produced. is obtained, and the flexibility and mechanical strength are significantly improved.

さらに電極反応表面積が著(2く増大し電池反応が,効
率よく、かつ均一に行われ、しかも電池反応により生じ
る生成物を電極近傍に保持することができ、多数回の充
放電サイクル等FlC}いても変形を生ずることなく優
れたアルカリ蓄電池用陰極が得られるというものである
。以下本発明の実施例について詳細に説明する。
In addition, the electrode reaction surface area is significantly increased (2 times larger, battery reactions are carried out efficiently and uniformly, and the products generated by the battery reactions can be retained near the electrodes, allowing for multiple charge/discharge cycles, etc.) Accordingly, an excellent cathode for an alkaline storage battery can be obtained without causing deformation even when the present invention is used.Examples of the present invention will be described in detail below.

本発明のアルカリ蓄電池陰極の製造方法は、活物質を亜
鉛とした場合、亜鉛活物質100fに対しフッ素樹脂の
水性分散体(デイスバージヨン)を8f1ポリアミドの
短繊維を0.5t,そして水30rと共に二ーダ混合機
で約15分間混練1−、粘土状物質を作り、この物質を
ローラにかけて圧延し、シート体を形成した。このシー
ト体はフツ素樹脂の繊維状の繊維体が圧延方向すなわち
繊維体の長手方向に整夕1ルて生じるので、シート体を
複数枚造り繊維体の整列方向を直交するように異ならし
て、重ね合せ再びローラーにかけて圧延する。この圧延
操作を繰り返えして行ない、充分な強度を有する活物質
のシート体を形成し、これを陰極集電体に圧着して陰極
を完成する。な}、耐アルカリ性短繊維は、ポリアミド
に限らず、ポリエチレン、ポリプロピレン、アクリロ[
ャgリルと塩化ピニールの共重合体などであつても良く
、短繊維の長さは余り短いと電極の変形を防ぐ効果が少
なく、長すぎると混線}よびロール展開時に困難を生じ
るので2〜15m!程度が適当であり、好ましくは5m
1前後であり、また短繊維の量が多すぎると活物質シー
ト体の多層構造を形成しにくくなるため活物質に対して
0.5(!l)程度が適当である。
In the method for producing an alkaline storage battery cathode of the present invention, when zinc is used as the active material, an aqueous dispersion of fluororesin (dice version) is added to 100 f of the zinc active material, 0.5 t of short fibers of 8 f1 polyamide, and 30 liters of water are added. The mixture was kneaded for about 15 minutes in a seconder mixer to form a clay-like material, and this material was rolled by rollers to form a sheet. In this sheet body, the fibrous bodies of fluororesin are aligned in the rolling direction, that is, the longitudinal direction of the fibrous bodies, so a plurality of sheet bodies are made and the alignment directions of the fibrous bodies are different so that they are orthogonal to each other. , overlap and roll again with rollers. This rolling operation is repeated to form a sheet of active material having sufficient strength, and this is pressed onto the cathode current collector to complete the cathode. }, alkali-resistant short fibers are not limited to polyamide, but also include polyethylene, polypropylene, acrylic [
It may also be a copolymer of carbon fiber and pinyl chloride. If the length of the short fibers is too short, it will have little effect in preventing deformation of the electrode, and if it is too long, it will cause cross-wires and difficulties when rolling out. 15m! Appropriate length, preferably 5m
If the amount of short fibers is too large, it becomes difficult to form a multilayer structure of the active material sheet, so the appropriate amount is about 0.5 (!l) for the active material.

このようにして得られた陰極をニツケル一亜鉛アルカリ
2次電池と1,て組立て亜鉛極の利用率を30%として
5時間率で充電し、5時間率で放電させる充放電サイク
ルを繰り返えした結果、第1図の実線1で示すような特
性が得られた。
Assemble the cathode thus obtained with a nickel-zinc alkaline secondary battery and repeat the charge-discharge cycle of charging at a 5-hour rate and discharging at a 5-hour rate with the zinc electrode utilization rate at 30%. As a result, characteristics as shown by solid line 1 in FIG. 1 were obtained.

この特性と比較するために短繊維に混入させない場合を
実線2で、亜鉛活物質100(Itに対しポリピニアル
コールを8V、そして水を80t加えてペースト状とし
て集電体に塗布して陰極ケ構成した従来の電池の場合を
実線3で示12た。この図から明らかなように本発明の
陰極を用いた電池の充放電サイクルが最も多いことが判
る。そして亜鉛極の利用率を60%とした場合には点線
で示すような特性となり、本発明の効果がさらに明確と
なる。な}第1図の特註を測定するにあたつて、対極の
影響を避けるために亜鉛極に対して大過剰のニツケル極
を用いた。そl−て電解液としては8Mの苛性カリを用
いた。
In order to compare with this characteristic, solid line 2 shows the case where the zinc active material is not mixed into the short fibers, and the zinc active material is 100% (8V for It, polypinial alcohol is added, and 80t of water is added to form a paste and applied to the current collector. The case of the conventional battery configured is shown by solid line 312.As is clear from this figure, it is clear that the battery using the cathode of the present invention has the most charge/discharge cycles.The utilization rate of the zinc electrode is 60%. In this case, the characteristics shown by the dotted line will be obtained, and the effect of the present invention will become even clearer.} When measuring the special notes in Figure 1, in order to avoid the influence of the opposite electrode, A large excess of nickel electrodes was used, and 8M caustic potassium was used as the electrolyte.

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

第1図は本発明の実施例で得られた特性と、参考例訃よ
び従来例で得られる特性を比較1,7た図である。
FIG. 1 is a comparison diagram of the characteristics obtained in the example of the present invention and the characteristics obtained in the reference example and the conventional example.

Claims (1)

【特許請求の範囲】[Claims] 1 陰極活物質と、フッ素樹脂の水性分散液と、耐アル
カリ性短繊維とからなる混練物を展開して繊維状シート
体を得る工程と、前記繊維状シート体の展開方向が異る
如く積層展開し、複数層に積層された繊維状シート体を
、集電体に着設する工程と具備したことを特徴とするア
ルカリ蓄電池用陰極の製造方法。
1. A step of developing a kneaded material consisting of a cathode active material, an aqueous dispersion of a fluororesin, and alkali-resistant short fibers to obtain a fibrous sheet body, and stacking and developing the fibrous sheet bodies so that the directions of the fibrous sheet bodies are different. A method for producing a cathode for an alkaline storage battery, comprising the step of attaching a fibrous sheet body laminated in multiple layers to a current collector.
JP50013334A 1975-02-03 1975-02-03 Cathode for alkaline batteries Expired JPS593027B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP50013334A JPS593027B2 (en) 1975-02-03 1975-02-03 Cathode for alkaline batteries

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP50013334A JPS593027B2 (en) 1975-02-03 1975-02-03 Cathode for alkaline batteries

Publications (2)

Publication Number Publication Date
JPS5189133A JPS5189133A (en) 1976-08-04
JPS593027B2 true JPS593027B2 (en) 1984-01-21

Family

ID=11830220

Family Applications (1)

Application Number Title Priority Date Filing Date
JP50013334A Expired JPS593027B2 (en) 1975-02-03 1975-02-03 Cathode for alkaline batteries

Country Status (1)

Country Link
JP (1) JPS593027B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6132837U (en) * 1984-07-31 1986-02-27 住友電気工業株式会社 disk rotor

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5580274A (en) * 1978-12-11 1980-06-17 Sanyo Electric Co Ltd Manufacturing method for cell plate
JP2692786B2 (en) * 1984-09-06 1997-12-17 三洋電機株式会社 Hydrogen storage electrode

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5132365B2 (en) * 1972-06-27 1976-09-11

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6132837U (en) * 1984-07-31 1986-02-27 住友電気工業株式会社 disk rotor

Also Published As

Publication number Publication date
JPS5189133A (en) 1976-08-04

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