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JPS5836834B2 - Manufacturing method for sealed storage batteries - Google Patents
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JPS5836834B2 - Manufacturing method for sealed storage batteries - Google Patents

Manufacturing method for sealed storage batteries

Info

Publication number
JPS5836834B2
JPS5836834B2 JP51055497A JP5549776A JPS5836834B2 JP S5836834 B2 JPS5836834 B2 JP S5836834B2 JP 51055497 A JP51055497 A JP 51055497A JP 5549776 A JP5549776 A JP 5549776A JP S5836834 B2 JPS5836834 B2 JP S5836834B2
Authority
JP
Japan
Prior art keywords
cathode
capacity
anode
battery
manufacturing
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
JP51055497A
Other languages
Japanese (ja)
Other versions
JPS52138644A (en
Inventor
利行 宇陀
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.)
Yuasa Corp
Original Assignee
Yuasa Battery Corp
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 Yuasa Battery Corp filed Critical Yuasa Battery Corp
Priority to JP51055497A priority Critical patent/JPS5836834B2/en
Publication of JPS52138644A publication Critical patent/JPS52138644A/en
Publication of JPS5836834B2 publication Critical patent/JPS5836834B2/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
    • 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

  • Secondary Cells (AREA)

Description

【発明の詳細な説明】 本発明は密閉型蓄電池の製法に関するもので、比較的簡
単な方法により高率放電特性、寿命特性などの性能良好
なる電池を提供するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a sealed storage battery, and provides a battery with good performance such as high rate discharge characteristics and life characteristics by a relatively simple method.

従来この種の電池においては陰極は陽極よりも充電容量
、放電容量共に大きい状態で封ロされるのが普通である
Conventionally, in this type of battery, the cathode is usually sealed with a larger charging capacity and discharging capacity than the anode.

これは過充電時、陰極に未充電部分を残すことにより水
素ガスの発生を抑制し、陽極から発生した酸素ガスを吸
収させて内部ガス圧の上昇を防止するためのものであり
、また長期に渡って充放電を繰り返すと、放電時に陰極
に生ずる反応生戒物が安定な結晶に成長し充電時に反応
し難くなり、容量が劣化するのに対処するためである。
This is to suppress the generation of hydrogen gas by leaving an uncharged portion on the cathode during overcharging, and to absorb oxygen gas generated from the anode to prevent an increase in internal gas pressure. This is to cope with the problem that when charging and discharging are repeated over a period of time, reaction substances generated at the cathode during discharging grow into stable crystals, making it difficult to react during charging and deteriorating the capacity.

このような陽極及び陰極の容量調整は封口前の化成工程
で行なわれるのが一般的であり、その一つの方法として
は含浸を終えた陽・陰極をそれぞれ化成して容量調整し
た後、積層して封ロするものがある。
This adjustment of the capacity of the anode and cathode is generally performed in a chemical formation process before sealing, and one method is to chemically form the anode and cathode after impregnation to adjust their capacity, and then stack them. There are some things that need to be sealed.

また他の一つの方法としては含浸を終えた陽・陰極をセ
パレータを介して積層し、化成して容量調した後封口す
るものがある。
Another method is to stack the impregnated anode and cathode with a separator interposed therebetween, chemically form the anode and cathode to adjust the capacity, and then seal the anode and cathode.

しかしながら前者においては陰極中の充電状態の活物質
が化或から封口までの間に空気中の酸素ガスにより容易
に酸化され容量調整が難しく、これを防止するために酸
素ガスのない雰囲気中で作業を行なったり、化成から組
立ての行程を迅速に行なう必要があった。
However, in the former case, the charged active material in the cathode is easily oxidized by oxygen gas in the air during the period from oxidation to sealing, making it difficult to adjust the capacity.To prevent this, work must be done in an atmosphere free of oxygen gas. It was necessary to carry out the processes from chemical formation to assembly quickly.

しかしながらこのようにして得た陰極においても各々の
容量のバラツキの発生を防止することは出来なかった。
However, even in the cathodes obtained in this manner, it was not possible to prevent variations in the respective capacities.

また、後者では、容量調整は比較的簡単であるが、工程
作業ともに複雑になり、電池のコストが大幅に上昇する
ことはまぬがれなかった。
In the latter case, although capacity adjustment is relatively simple, the process becomes complicated and the cost of the battery inevitably increases significantly.

本発明は、前記欠点を解消しようとするものであり、一
方の陰極板を完全放電状態とする工程と、他方の陰極板
を充電状態とする工程と、前記のそれぞれの陰極板を電
気的に接触させた陰極と該陰極よりも容量の小なる完全
放電状態の陽極とをセパレータを介して積層し容器内に
収納する工程とを有することを特徴とするものである。
The present invention aims to eliminate the above drawbacks, and includes a step of bringing one cathode plate into a fully discharged state, a step of bringing the other cathode plate into a charged state, and electrically connecting each of the cathode plates. This method is characterized by the step of stacking a cathode in contact with a fully discharged anode having a smaller capacity than the cathode with a separator in between, and storing the stack in a container.

以下本発明をニッケルを陽極活物質、カドミウムを陰極
活物質とした巻同極板に採用したー実施例につき説明す
る。
Hereinafter, an embodiment will be described in which the present invention is applied to a wound plate in which nickel is used as an anode active material and cadmium is used as a cathode active material.

ニッケル粉を焼結して得た多孔性基板に、陽板は硝酸ニ
ッケルあるいは塩化カドミウムの溶液を含浸し、次にア
ルカリ性溶液中で陰電解あるいは中和して水酸化物を得
る。
A porous substrate obtained by sintering nickel powder is impregnated with a solution of nickel nitrate or cadmium chloride, and then subjected to negative electrolysis or neutralization in an alkaline solution to obtain hydroxide.

次に水洗して基板中のアルカリ分を除去してのち乾燥す
る。
Next, the substrate is washed with water to remove the alkali content in the substrate, and then dried.

この工程を7〜8回繰り返して基板中に活物質を所定量
充填させる。
This process is repeated 7 to 8 times to fill the substrate with a predetermined amount of active material.

このようにして得た陽・陰極は活物質の活性及び不純物
の除去及び容量調整の目的からそれぞれ化成を行なう。
The anode and cathode thus obtained are subjected to chemical formation for the purpose of activating the active material, removing impurities, and adjusting the capacity.

陽極は0.1〜0.2Cの電流で充放電1サイクルを行
なって完全放電状態にしたのち水洗と乾燥とを行なう。
The anode is subjected to one charging/discharging cycle with a current of 0.1 to 0.2 C to bring it into a fully discharged state, and then washed with water and dried.

陰極は2分割し、この一方の陰極板は陽極と同じように
0.1〜0.2Cの電流で充放電を1サイクル行ない完
全放電状態にしたのち水洗と乾燥をする。
The cathode is divided into two parts, and one of the cathode plates is charged and discharged for one cycle with a current of 0.1 to 0.2C in the same way as the anode, and after being completely discharged, it is washed with water and dried.

また他方の陰極板は0.1〜0.2Cの電流で充電ある
いは充放電数回繰返したのち充電を行い充電状態にした
のち水洗乾燥する。
The other cathode plate is charged with a current of 0.1 to 0.2 C, or charged and discharged several times, and then charged to a charged state, and then washed with water and dried.

しかし充電状態の陰極板における金属カドミウムを通常
の水洗と乾燥とをすると、水洗で約10%,乾燥で60
〜70φが酸素ガス及び水と反応して水酸化カドミウム
となってしまう。
However, when the metal cadmium in the cathode plate in a charged state is washed with water and dried in the normal way, it is about 10% when washed with water and 60% when dried.
~70φ reacts with oxygen gas and water and becomes cadmium hydroxide.

すなわち乾′吟工程において、大気中でも容易に酸化す
る金属カドミウムを、充分酸素ガス及び水分が存在する
雰囲気中で温度を上げるごとく行えば、乾燥時間は短か
くてすむが、酸化が促進する。
That is, in the drying process, if the temperature of metal cadmium, which is easily oxidized even in the atmosphere, is carried out in an atmosphere containing sufficient oxygen gas and moisture, the drying time will be shortened, but oxidation will be accelerated.

また温度をさげても乾燥時間が長くなって同程度酸化し
てしまう。
Furthermore, even if the temperature is lowered, the drying time becomes longer and oxidation occurs to the same extent.

そこで乾燥を真空中で行なえば乾燥時間は短かくなり酸
素ガスがほとんどない状態で乾燥するため酸化がほとん
ど進行しないことがわかった。
Therefore, it was found that if drying is carried out in a vacuum, the drying time will be shortened and oxidation will hardly proceed because the drying is carried out in the absence of oxygen gas.

このようにして真空乾燥した充電状態※※の陰極板は湿
度の低い雰囲気あるいは酸素ガスのない雰囲気中に保存
する。
The vacuum-dried cathode plate in a charged state※※ is stored in an atmosphere with low humidity or an atmosphere without oxygen gas.

続いて放電状態の陰極板と充電状態の陰極板とを電気的
に接触させ、放電状態にした陽極とをセパレーターを介
して巻回すると共に金属容器に収納する。
Subsequently, the cathode plate in the discharged state and the cathode plate in the charged state are brought into electrical contact, and the anode in the discharged state is wound together with a separator interposed therebetween and housed in a metal container.

このようにして得られた電池と従来の電池とを公称容量
1 2 0 0 mAHの電池で、各電流で放電した時
の平均放電容量につき、その初期容量と正規充放電の2
0サイクル目の容量において比較したものを表−1に示
す。
The battery thus obtained and the conventional battery have a nominal capacity of 1200 mAH, and the average discharge capacity when discharging at each current is the initial capacity and 2 of the normal charge and discharge.
Table 1 shows a comparison of the capacities at the 0th cycle.

尚、試料1は従来の電池において含浸を終えた陽・陰極
をそれぞれ化成して容量調整したのち、巻込んで封ロし
た電池、2は同じく従来の電池において含浸を終えた陽
・陰極を巻込んで、化成して容量調整したのち封ロした
電池であり、3は本発明による前記方法で製作した電池
である。
Sample 1 is a battery in which the anode and cathode of a conventional battery have been chemically formed to adjust the capacity, and then rolled up and sealed. No. 3 is a battery manufactured by the method described above according to the present invention.

続いて表−2に表−1に基づき、それぞれの容量を同一
試料での0.20放電の初期容量に対する容量比をパー
セントで示ス。
Next, Table 2 shows the capacity ratio of each capacity to the initial capacity of 0.20 discharge in the same sample as a percentage based on Table 1.

以上の結果より明らかなごとく本発明による方法で製作
した電池は高率放電特性、寿命特性において良好なもの
が得られることが分かる。
As is clear from the above results, it can be seen that the battery manufactured by the method of the present invention has good high rate discharge characteristics and good life characteristics.

尚、本発明による方法で製作した電池が、試料1で示さ
れる方法により製作された電池に比較して諸特性が良い
理由は、試料1で示されるものの容量調整が難しくバラ
ツキが多いのに対し、本発明によるものは確実に容量調
整がなされているためであろうと思はわれる また試料2で示される方法により製作された電池は諸特
性においては本発明によるものと同程度であるが、製造
工程が複雑でありコストが高くなる点に欠点がある。
The reason why the battery manufactured by the method according to the present invention has better characteristics than the battery manufactured by the method shown in Sample 1 is that while the capacity adjustment of the battery shown in Sample 1 is difficult and there are many variations. This seems to be because the capacity of the battery according to the present invention is reliably adjusted.Furthermore, the battery manufactured by the method shown in Sample 2 has the same characteristics as the battery according to the present invention, but The disadvantage is that the process is complicated and the cost is high.

尚、本発明の一実施例として製造工程の途中で分割した
例を示したが、最初から分割した極板を用いても伺ら本
発明の要旨を逸脱するものではない0 以上、本発明は比較的簡単な製法により高率放電特性や
寿命特性の良好なる電池を提供するものである。
Although an example in which the electrode plates are divided in the middle of the manufacturing process is shown as an embodiment of the present invention, it does not deviate from the gist of the present invention even if the electrode plates are divided from the beginning. The present invention provides a battery with good high rate discharge characteristics and long life characteristics using a relatively simple manufacturing method.

Claims (1)

【特許請求の範囲】[Claims] 1 一方の陰極板を完全放電状態とする工程と、他方の
陰極板を充電状態とする工程と、前記それぞれの陰極板
を電気的に接触させた陰極と該陰極よりも容量の小なる
完全放電状態の陽極とをセパレータを介して積層して金
属容器内に収納する工程とを有することを特徴とする密
閉型蓄電池の製法。
1 A step of bringing one cathode plate into a fully discharged state, a step of bringing the other cathode plate into a charged state, and a cathode with a smaller capacity than the cathode in which each of the cathode plates is brought into electrical contact with the cathode, and a complete discharge with a smaller capacity than the cathode. 1. A method for manufacturing a sealed storage battery, comprising the steps of stacking a positive electrode and an anode with a separator interposed therebetween and storing the same in a metal container.
JP51055497A 1976-05-14 1976-05-14 Manufacturing method for sealed storage batteries Expired JPS5836834B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51055497A JPS5836834B2 (en) 1976-05-14 1976-05-14 Manufacturing method for sealed storage batteries

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51055497A JPS5836834B2 (en) 1976-05-14 1976-05-14 Manufacturing method for sealed storage batteries

Publications (2)

Publication Number Publication Date
JPS52138644A JPS52138644A (en) 1977-11-18
JPS5836834B2 true JPS5836834B2 (en) 1983-08-11

Family

ID=13000270

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51055497A Expired JPS5836834B2 (en) 1976-05-14 1976-05-14 Manufacturing method for sealed storage batteries

Country Status (1)

Country Link
JP (1) JPS5836834B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01112317U (en) * 1988-01-20 1989-07-28

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01112317U (en) * 1988-01-20 1989-07-28

Also Published As

Publication number Publication date
JPS52138644A (en) 1977-11-18

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