JPS6037653A - Manufacture of alkaline battery - Google Patents
Manufacture of alkaline batteryInfo
- Publication number
- JPS6037653A JPS6037653A JP14582883A JP14582883A JPS6037653A JP S6037653 A JPS6037653 A JP S6037653A JP 14582883 A JP14582883 A JP 14582883A JP 14582883 A JP14582883 A JP 14582883A JP S6037653 A JPS6037653 A JP S6037653A
- Authority
- JP
- Japan
- Prior art keywords
- zinc
- battery
- solution
- negative electrode
- punched
- 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.)
- Pending
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/06—Electrodes for primary cells
- H01M4/08—Processes of manufacture
- H01M4/12—Processes of manufacture of consumable metal or alloy electrodes
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、アルカリ電池、特にその負極の製造法に関す
る。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to an alkaline battery, and in particular to a method for manufacturing its negative electrode.
従来例の構成とその問題点
エレクトロニクスの発展に伴い、ウォッチの動作も重子
回路によるものが主流となり、時計の精度は格段に向上
した。今日のウォッチはそれに加え、フアツシヨン性を
意識した小形、薄形が要求されている。それにより、そ
の電源としてのアルカリ電池も小形、薄形が要求されて
いる。Conventional configurations and their problems With the development of electronics, the operation of watches has become mainstream using multiple circuits, and the accuracy of watches has improved significantly. In addition to this, today's watches are required to be small and thin with fashion in mind. Accordingly, the alkaline batteries used as the power source are also required to be small and thin.
従来、アルカリ電池の負極活物質には粉末の水化亜鉛が
用いられでいる。電池を量産する場合、粉末水化亜鉛は
、ある一定容積をもった容器で計りとる所謂折きりによ
って計量し、負極容器に充填していた。この方法では、
秤量バラツキはL:2m2程度であり、この誤差による
容量のバラツキは約smAh である。現在、C2モス
LSIを用いた時計1分針のみの単機能ウォッチの消費
電力は年間約5mAh 以下となっておシ、電源の作動
期間は約2年が要求されているが、この容911゜m、
Ah からして、粉末水化亜鉛による。pli 、i;
jのバラツキは30%の容量誤差を招くことになる。Conventionally, powdered zinc hydrate has been used as the negative electrode active material of alkaline batteries. When mass-producing batteries, powdered zinc hydrate was weighed in a container with a certain volume, so-called folding, and filled into a negative electrode container. in this way,
The weighing variation is about L:2m2, and the capacity variation due to this error is about smAh. Currently, the power consumption of a single-function watch with only a one-minute hand using C2MOS LSI is approximately 5 mAh or less per year, and the power supply is required to operate for approximately 2 years. ,
From Ah, due to powdered zinc hydrate. pli,i;
Variation in j results in a 30% capacity error.
その結果、電池の容量設計もバラツキを考慮し、理想状
態よりも3o%もダウンし/こかたちになる。As a result, the battery capacity design also takes into account variations, resulting in a 30% lower capacity than the ideal state.
まだ、扁平電池の場合、計量され負極容器に入れられた
山状になった粉末水化亜鉛を一度、薄い容器内に均一に
ならす工程が必要であるが、均一・にならずことは量産
工程ではかなり困難な作業である。亜鉛薄板を円状に打
ち抜き、これを活物質とすれば秤量バラツキは±0.2
mg程度となる。In the case of flat batteries, there is still a process in which the mountain-shaped powdered zinc hydrate that is weighed and placed in the negative electrode container is leveled uniformly in the thin container, but this is not possible during the mass production process. This is quite a difficult task. If a thin zinc plate is punched out into a circular shape and this is used as the active material, the weighing variation will be ±0.2
It will be about mg.
従って、電池の容量設営1におし・てバラツキをほとん
ど考慮する必要がなく、実質的な容量アンプが可能であ
る。しかし、表面積が粉末に比べ1/10以下にもなり
、電池性能、特にパルス放電特性が悪くなる不都合があ
る。Therefore, there is almost no need to consider variations in battery capacity setting 1, and a substantial capacity amplifier is possible. However, the surface area is less than 1/10 of that of powder, which causes the disadvantage that battery performance, especially pulse discharge characteristics, deteriorates.
亜鉛薄板をエキスバンド状にして表面積を広くしだもの
を打ち抜いて用いることは、電池性能を落とすことなく
、秤量精度向上により実質な容量アップができることは
従来よりいわれているが、実用的に無理な点が多かった
。It has been said for some time that using a thin zinc plate in the form of an expanded band with a wider surface area and punching it out can substantially increase capacity by improving weighing accuracy without degrading battery performance, but this is not practical. There were many points.
すなわち、亜鉛を用いるアルカリ電池は電解液による亜
鉛の腐食溶解に伴う水素ガスの発生があり自己放電が促
進される。That is, in an alkaline battery using zinc, self-discharge is promoted due to the generation of hydrogen gas due to the corrosion and dissolution of zinc by the electrolyte.
これを防ぐ対策として水素過電斥を高く維持させるのに
水銀によって一定量の水化が必要であるが、あらかじめ
水化した亜鉛は非常にもろく、エキスバンド状になって
いる亜鉛も、その形状を量産工程において保つことはで
きず、ましてや打ち抜きで粉々となってしまう。As a countermeasure to prevent this, a certain amount of hydration with mercury is necessary to maintain a high hydrogen overcharge, but zinc that has been hydrated in advance is extremely brittle, and zinc that is in the form of an expanded band is difficult to maintain due to its shape. It is impossible to maintain this during the mass production process, and even more so, it will break into pieces during punching.
エキスバンド状亜鉛を打ち抜き、HqO等の水銀化合物
粉体を加え、負極容器内で水化する方法もあるが、これ
は、水銀化合物の秤量誤差が亜鉛の容量バラツギを招き
、水化反応においてZnO等の生成物がかなり多くでき
るだめ、それが電池の性能、信頼性を損なうので実用的
でなかった。There is also a method of punching expanded banded zinc, adding powder of a mercury compound such as HqO, and hydrating it in a negative electrode container. However, this method was impractical because it produced a large amount of products such as the following, impairing the performance and reliability of the battery.
発明の目的
本発明は、上記従来例の欠点をなくし、高容鼠で薄形の
アルカリ電池を与える負極の製造法を提供することを目
的とする。OBJECTS OF THE INVENTION It is an object of the present invention to provide a method for producing a negative electrode that eliminates the drawbacks of the above-mentioned conventional examples and provides a thin alkaline battery with high capacity.
発明の構成
本発明は、亜鉛のエキスバンドメタル寸だはパンチンク
メタルを所定の大きさに打ち抜き、これを水銀化合物、
例えばHqC12の水溶液中に浸漬し、所定量の水化を
行った後、水洗、乾燥後、負極容器に充填し電解液を注
液・し、正極と組み合わせて電池を構成するものである
。Structure of the Invention The present invention involves punching a punched metal of zinc into a predetermined size, and then punching the punched metal into a predetermined size.
For example, it is immersed in an aqueous solution of HqC12, hydrated to a predetermined amount, washed with water, dried, then filled into a negative electrode container, filled with electrolyte, and combined with a positive electrode to form a battery.
ここで、電解液には封口直前まで負極内面からの水素ガ
ス発生を抑制するため、HqOを飽和させる程度に溶解
させたものを用いるのが好ましい。Here, in order to suppress the generation of hydrogen gas from the inner surface of the negative electrode until immediately before sealing, it is preferable to use an electrolytic solution in which HqO is dissolved to a saturation degree.
実施例の説明
エキスバンド加工した開口率90%、単位面積あたりの
重量43.11ng/crl の純亜鉛板を直径6.3
m1l+の円板状に打ち抜いたものを、1o重量%のH
qC12水溶液中に浸漬し、攪拌しながら10重量%に
氷化されるように浸漬時間を調整する。これを取り出し
て水洗、乾燥した後、負極容器へ充填し、次いで亜鉛上
に含液拐をのせ、か性カリの40重量%水溶液にHqO
を飽和させた電解液を9μl注液し、30秒間水化する
のを待って、セパレータをのせた正極部と合わせ封口し
た。Description of Example A pure zinc plate with a diameter of 6.3 mm and an aperture ratio of 90% and a weight per unit area of 43.11 ng/crl was
Punch out a disk shape of m1l+ and add 10% by weight of H.
It is immersed in a qC12 aqueous solution, and the immersion time is adjusted while stirring so that it is frozen to 10% by weight. After taking it out, washing it with water, and drying it, it was filled into a negative electrode container. Then, a liquid-containing plate was placed on the zinc, and a 40% by weight aqueous solution of caustic potash was added with HqO.
9 μl of an electrolytic solution saturated with was injected, and after waiting for hydration for 30 seconds, it was combined with a positive electrode portion on which a separator was placed and sealed.
第1図は、上記の方法によって得た5R910(直径9
.2mm、総高1 、Oynm、 )のボタン形アルカ
リ電池を示す。Figure 1 shows 5R910 (diameter 9
.. A button-shaped alkaline battery with a total height of 2 mm and a total height of 1 mm is shown.
図中、1はニッケルメッキした鉄製の正極ケース、2は
酸化銀97重量%と銀粉3重量%からなる正極ペン、ト
、3はセパレータ、4は含液材、5は水化亜鉛負極であ
る。6は内面に銅層を有する負極容器をかねた封目板、
7はナイロンよりなるガスケットである。In the figure, 1 is a positive electrode case made of nickel-plated iron, 2 is a positive electrode pen made of 97% by weight of silver oxide and 3% by weight of silver powder, 3 is a separator, 4 is a liquid-containing material, and 5 is a zinc hydrate negative electrode. . 6 is a sealing plate having a copper layer on the inner surface and serving as a negative electrode container;
7 is a gasket made of nylon.
第2図は上記の実施例に示した本発明による電池Aと、
水化亜鉛粉末を負極に用いた電池Bについて、30 K
、G’の負荷で放電したときの放電カーブを示す。斜
線部は電池10個の特性のバラツキを示す。電池Aは電
池Bに比べて、高容計でバラツキが少ないことがわかる
。FIG. 2 shows a battery A according to the invention shown in the above embodiment,
For battery B using zinc hydrate powder as the negative electrode, 30 K
, shows a discharge curve when discharging with a load of G'. The shaded area indicates variations in the characteristics of the 10 batteries. It can be seen that battery A has a higher capacity and less variation than battery B.
上記実施例では、酸化水銀を溶解した電解液を負極側に
注液した。これは、負極容器内面の水化を行わせると共
に、エキスバンド亜鉛負極の水化の十分進んでいない部
分の水化を助けることにより、ガス発生を防止するため
であり、負極容器内面を予め水化処理して電池を組立て
る場合は酸化水銀を電解液に加える必要はない。In the above example, an electrolytic solution in which mercury oxide was dissolved was injected into the negative electrode side. This is to prevent gas generation by hydrating the inner surface of the negative electrode container and helping to hydrate the parts of the expanded zinc negative electrode that are not sufficiently hydrated. When assembling a battery by chemical treatment, it is not necessary to add mercury oxide to the electrolyte.
また、負極亜鉛にはエキスバンド加工したものを用いた
が、多数の微孔を打ち抜き形成したものでも、秤量精度
および表面積の点で同等の効果が得られる。Further, although expanded band processed negative electrode zinc was used, the same effect in terms of weighing accuracy and surface area can be obtained even if a large number of fine holes are punched out.
又、エキスバンド亜鉛の打ち抜き品をHqCIJ2水溶
液で水化処理したものを実施例では示したが、HqC7
1又はHqCNでも同等の効果が得られる。In addition, although the example shows a punched product of extracted band zinc that has been hydrated with a HqCIJ2 aqueous solution, HqC7
The same effect can be obtained with 1 or HqCN.
発明の効果
以上のように、本発明は亜鉛のパンチングメタルまたは
エキスバンドメタルを用い、水銀化合物の水溶液で水化
処理をするので、一度に多量の氷化処理ができ、かつ均
一に水化される。このだめ、電池設計において、計量バ
ラツキの考慮を極少にすることができ、実質的な高容量
化ができ、特に超小形、薄形電池において効果は著しい
。Effects of the Invention As described above, the present invention uses punched metal or expanded metal of zinc and performs hydration treatment with an aqueous solution of a mercury compound, so that a large amount of ice can be treated at one time and hydrated uniformly. Ru. Therefore, in battery design, consideration of measurement variations can be minimized, and the capacity can be substantially increased, which is particularly effective in ultra-small and thin batteries.
第1図は本発明の一実施例のアルカリ電池の一部を断面
にした側面図、第2図は電池の特性比較図である。FIG. 1 is a partially sectional side view of an alkaline battery according to an embodiment of the present invention, and FIG. 2 is a comparison diagram of battery characteristics.
Claims (2)
ルを所定の大きさに切断した後、水銀化合物の水溶液に
より水化させる工程を有するアルカリ電池の製造法。(1) A method for producing an alkaline battery, which includes the step of cutting expanded metal or punched metal of zinc into a predetermined size, and then hydrating it with an aqueous solution of a mercury compound.
である特許請求の範囲第1項記載のアルカリ電池の製造
法。(2) The method for producing an alkaline battery according to claim 1, wherein the mercury compound is mercury chloride or mercury cyanide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14582883A JPS6037653A (en) | 1983-08-10 | 1983-08-10 | Manufacture of alkaline battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14582883A JPS6037653A (en) | 1983-08-10 | 1983-08-10 | Manufacture of alkaline battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6037653A true JPS6037653A (en) | 1985-02-27 |
Family
ID=15394055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14582883A Pending JPS6037653A (en) | 1983-08-10 | 1983-08-10 | Manufacture of alkaline battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6037653A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8291785B2 (en) | 2007-12-25 | 2012-10-23 | Jtekt Corporation | Ball screw |
-
1983
- 1983-08-10 JP JP14582883A patent/JPS6037653A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8291785B2 (en) | 2007-12-25 | 2012-10-23 | Jtekt Corporation | Ball screw |
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