JPH0465500B2 - - Google Patents
Info
- Publication number
- JPH0465500B2 JPH0465500B2 JP58099215A JP9921583A JPH0465500B2 JP H0465500 B2 JPH0465500 B2 JP H0465500B2 JP 58099215 A JP58099215 A JP 58099215A JP 9921583 A JP9921583 A JP 9921583A JP H0465500 B2 JPH0465500 B2 JP H0465500B2
- Authority
- JP
- Japan
- Prior art keywords
- positive electrode
- electrode mixture
- separator
- porous body
- core rod
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/04—Cells with aqueous electrolyte
- H01M6/06—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
- H01M6/08—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with cup-shaped electrodes
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Primary Cells (AREA)
Description
本発明は筒形アルカリ電池の製造法の改良に係
り、正極合剤への電解液の浸潤を促進して製造時
間の短縮を図るとともに、電池特性の向上を図る
ことを目的とする。
筒形アルカリ・マンガン電池などの筒形アルカ
リ電池では、筒状の正極合剤の中空部にコツプ状
に加工されたセパレータを挿入し、該セパレータ
の中空部に電解液を注入してセパレータと正極合
剤の密着を図るとともに電解液を正極合剤に浸潤
させる方法が採られている。ところで、このよう
な方法による場合、正極合剤の中空部へのセパレ
ータを挿入を容易にするためにセパレータの外径
が正極合剤の内径より若干小さく設計されている
ことや、セパレータをコツプ状に加工する際の寸
法バラツキなどによつて、正極合剤とセパレータ
の間に空隙が生じやすく、そのため、セパレータ
内に注入した電解液が正極合剤に浸潤していくの
が遅くなつて製造時間が長くなつたり、電池特性
の低下を来すなどの問題があつた。
本発明は上述した従来技術の欠点を解消するも
ので、正極缶への正極合剤の圧着に際し、正極合
剤とコアロツドとの間に保液性を有する多孔体を
介在させて正極合剤を上方から加圧し、正極合剤
を正極缶に圧着後、コアロツドを引き抜き、上記
多孔体が形成する筒状部の中空部セパレータを挿
入することによつて、電解液の正極合剤への浸潤
を促進させ、電池特性を向上させて、目的を達成
したものである。
すなわち、本発明の方法によれば、正極合剤は
前記加圧により多孔体にも圧接して、合剤粒子が
多孔体の孔中に入り込んでいるので、多孔体との
密着が充分であり、またセパレータと多孔体との
間は、セパレータ内への電解液の注入によつてセ
パレータと多孔体とが膨潤して密着するため、密
着性が非常に良好になり、そのため、従来法で見
られたような正極合剤とセパレータとの間の空隙
がなくなり、その結果、電解液の浸潤速度がはや
くなり、かつ正極合剤とセパレータとの間のイオ
ン伝導がよくなつて、内部抵抗が減少し、重負荷
特性が向上する。
本発明において用いる保液性を有する多孔体と
しては、例えばビニロンーレーヨン混抄紙、ビニ
ロン不織布、レーヨン不織布、マーセル化コツト
ン不織布、ポリプロピレン不織布、ポリアミド不
織布、ビニヨン不織布、ビニロンーマーセル化コ
ツトン混抄紙、マーセル化パルプ不織布、リンタ
ーパルプレーヨン混抄紙などが用いられる。これ
らの多孔体はできるだけセパレータの同材質のも
のを用いるのが好ましい。また保液性を有しない
ものは、電解液の浸潤に要する時間が長くなり、
また内部抵抗の増加を引き起こすので好ましくな
い。
次に本発明の実施例を図面とともに説明する。
実施例
ニツケルメツキを施した鉄製正極缶1に、二酸
化マンガンと黒鉛とからなる正極合剤粉末を加圧
成形したリング状の正極合剤成形体を正極缶1の
内壁に沿つて4個積み重ねて収納し、それら正極
合剤の中空部に多孔体としての厚さ0.10mmのビニ
ロンーレーヨン混抄紙で形成した筒状部を有する
コツプ状物2を前記正極合剤の中空部内壁に沿つ
て挿入し、ついで該コツプ状物2の中空部内壁に
沿つてコアロツド21を挿入し、コアロツド21
の外周に摺動自在に装着したパンチ22を下降さ
せて正極合剤を上方から加圧して、正極合剤3を
正極缶1の内壁に圧着させた(第1図参照)。
圧着後、パンチ22を引き上げ、ついでコアロ
ツド21を引き抜き、正極缶1の開口部を屈曲さ
せて、その開口端近傍に溝を形成した後、前記多
孔体としてのビニロンーレーヨン混抄紙を筒状部
2aとするコツプ状物2の中空部に、厚さ0.15mm
のビニロンーレーヨン混抄紙を3重巻きして形成
した筒状のセパレータ4を挿入し、ついで過剰の
電解液17をセパレータ4内に注入し(第2図参
照)、30分間放置して電解液をセパレータ4、正
極合剤3などに浸潤させた。その後、吸引ノズル
により余剰の電解液をセパレータ4内から取り除
いた。30分間で浸潤した電解液量は1.7gであつ
た。
次に、正極缶1のセパレータ4内に汞化亜鉛粉
末を電解液に分散させた負極剤5を充填し、つい
で負極リード棒6およびワツシヤ7を装着した合
成樹脂製封口体8を正極缶1の開口部に挿入し、
正極缶1の溝から先の部分を半径方向に締め付け
て封口体8に密着させ正極缶1の開口部を封口し
た。以下、常法により外装を施し、第3図に示す
ようなLR6形のアルカリ・マンガン電池Aを製造
した。第3図中、9は板ばねであり、10は負極
端子板、11は絶縁リング、12,13は樹脂チ
ユーブ、14は正極端子板、15は金属外装缶、
16は絶縁リングである。
比較例
実施例と同様の正極缶1に、実施例と同様の組
成の正極合剤粉末を加圧成形したリング状の正極
合剤成形体を実施例と同様に4個積み重ねて収納
し、その中空部にコアロツド21を挿入し、コア
ロツド21の外周に摺動自在に装着したパンチ2
2を下降させて正極合剤を上方から加圧して、正
極合剤3を正極缶1の内壁に圧着させた(第4図
参照)。
圧着後、パンチ22を引き上げ、ついでコアロ
ツド21を引き抜き、正極缶1の開口部を屈曲さ
せて、その開口端近くに溝を形成した後、正極合
剤3の中空部に筒状部を厚さ0.15mmのビニロンー
レーヨン混抄紙を3重巻きにして形成したコツプ
状のセパレータ4を挿入し、該セパレータ4内に
過剰の電解液を注入し、45分間放置して電解液を
セパレータ4および正極合剤3に浸潤させた。そ
の後、吸引ノズルにより余剰の電解液をセパレー
タ4から取り除いた。45分間で浸潤した電解液量
は1.6gであつた。
以後、常法に従つてLR6形のアルカリ・マンガ
ン電池Bを製造した。
上記のようにして製造された電池AおよびBの
浸潤に要した時間および浸潤された電解液量を第
1表に示す。また電池AおよびBの内部抵抗およ
び−10℃、2Ω間欠放電(5秒放電/5秒休止)
での終止電圧0.9Vまでの放電時間(正味放電時
間)を測定した結果を第2表に示す。
The present invention relates to an improvement in the manufacturing method of a cylindrical alkaline battery, and aims to shorten manufacturing time by promoting infiltration of an electrolytic solution into a positive electrode mixture, and to improve battery characteristics. In cylindrical alkaline batteries such as cylindrical alkaline and manganese batteries, a separator processed into a pot is inserted into the hollow part of the cylindrical positive electrode mixture, and an electrolyte is injected into the hollow part of the separator to separate the separator and the positive electrode. A method has been adopted in which the positive electrode mixture is infiltrated with an electrolytic solution while the mixture is made to adhere closely. By the way, when using such a method, the outer diameter of the separator is designed to be slightly smaller than the inner diameter of the positive electrode mixture in order to facilitate insertion of the separator into the hollow part of the positive electrode mixture, and the separator is designed to be shaped like a tap. Due to dimensional variations during processing, gaps tend to form between the positive electrode mixture and the separator, which slows down the electrolyte injected into the separator and infiltrates the positive electrode mixture, resulting in longer manufacturing times. There were problems such as longer battery life and deterioration of battery characteristics. The present invention solves the above-mentioned drawbacks of the prior art, and when press-bonding the positive electrode mixture to the positive electrode can, a porous body having a liquid retaining property is interposed between the positive electrode mixture and the core rod. Pressure is applied from above and the positive electrode mixture is crimped onto the positive electrode can, then the core rod is pulled out and the hollow separator of the cylindrical part formed by the porous body is inserted to prevent the electrolyte from infiltrating into the positive electrode mixture. The purpose was achieved by promoting the battery and improving battery characteristics. That is, according to the method of the present invention, the positive electrode mixture also comes into pressure contact with the porous body due to the pressurization, and the mixture particles enter the pores of the porous body, so that the adhesion with the porous body is sufficient. In addition, the adhesion between the separator and the porous body is very good because the electrolyte injected into the separator causes the separator and the porous body to swell and come into close contact with each other. As a result, the gap between the positive electrode mixture and the separator is eliminated, and as a result, the infiltration rate of the electrolyte becomes faster, and the ionic conduction between the positive electrode mixture and the separator improves, reducing internal resistance. and improves heavy load characteristics. Porous materials having liquid-retentive properties used in the present invention include, for example, vinylon-rayon mixed paper, vinylon non-woven fabric, rayon non-woven fabric, mercerized cotton non-woven fabric, polypropylene non-woven fabric, polyamide non-woven fabric, vinylon non-woven fabric, vinylon-mercerized cotton mixed paper, mercer. Non-woven fabric made from treated pulp, linter pulp rayon mixed paper, etc. are used. It is preferable that these porous bodies be made of the same material as the separator. In addition, those that do not have liquid retention properties require a longer time for electrolyte to infiltrate.
It is also undesirable because it causes an increase in internal resistance. Next, embodiments of the present invention will be described with reference to the drawings. Example: In a nickel-plated iron positive electrode can 1, four ring-shaped positive electrode mixture molded bodies made by pressure-molding positive electrode mixture powder made of manganese dioxide and graphite are stacked and stored along the inner wall of the positive electrode can 1. Then, a pot 2 having a cylindrical part made of vinylon-rayon mixed paper with a thickness of 0.10 mm as a porous body was inserted into the hollow part of the positive electrode mixture along the inner wall of the hollow part of the positive electrode mixture. Then, the core rod 21 is inserted along the inner wall of the hollow part of the tip 2, and the core rod 21 is
A punch 22 slidably attached to the outer periphery of the can was lowered to apply pressure to the positive electrode mixture from above, thereby pressurizing the positive electrode mixture 3 to the inner wall of the positive electrode can 1 (see FIG. 1). After crimping, pull up the punch 22, then pull out the core rod 21, bend the opening of the positive electrode can 1, form a groove near the opening end, and then insert the vinylon-rayon mixed paper as the porous body into a cylindrical part. A thickness of 0.15 mm is placed in the hollow part of the pot-like object 2 called 2a.
A cylindrical separator 4 made by wrapping vinylon-rayon mixed paper three times is inserted, and then excess electrolyte 17 is injected into the separator 4 (see Figure 2), and left for 30 minutes to dissolve the electrolyte. was infiltrated into the separator 4, positive electrode mixture 3, etc. Thereafter, excess electrolyte was removed from the separator 4 using a suction nozzle. The amount of electrolyte infiltrated in 30 minutes was 1.7 g. Next, the separator 4 of the positive electrode can 1 is filled with a negative electrode material 5 in which zinc chloride powder is dispersed in an electrolytic solution, and then the synthetic resin sealing body 8 to which the negative electrode lead rod 6 and washer 7 are attached is attached to the positive electrode can 1. insert it into the opening of
The opening of the positive electrode can 1 was sealed by tightening the portion of the positive electrode can 1 beyond the groove in the radial direction to bring it into close contact with the sealing body 8. Thereafter, the exterior was applied by a conventional method to produce an LR6 type alkaline manganese battery A as shown in Fig. 3. In Fig. 3, 9 is a leaf spring, 10 is a negative terminal plate, 11 is an insulating ring, 12 and 13 are resin tubes, 14 is a positive terminal plate, 15 is a metal exterior can,
16 is an insulating ring. Comparative Example In the same positive electrode can 1 as in the example, four ring-shaped positive electrode mixture molded bodies obtained by pressure-molding the positive electrode mixture powder with the same composition as in the example were stacked and stored in the same manner as in the example. A core rod 21 is inserted into the hollow part, and a punch 2 is slidably attached to the outer periphery of the core rod 21.
2 was lowered to pressurize the positive electrode mixture from above, and the positive electrode mixture 3 was pressed onto the inner wall of the positive electrode can 1 (see FIG. 4). After crimping, pull up the punch 22, then pull out the core rod 21, bend the opening of the positive electrode can 1, form a groove near the opening end, and then insert a cylindrical part into the hollow part of the positive electrode mixture 3. Insert a pot-shaped separator 4 formed by wrapping 0.15 mm vinylon-rayon mixed paper in three layers, inject excess electrolyte into the separator 4, and leave it for 45 minutes to distribute the electrolyte between the separator 4 and the positive electrode. Mixture 3 was infiltrated. Thereafter, excess electrolyte was removed from the separator 4 using a suction nozzle. The amount of electrolyte infiltrated in 45 minutes was 1.6 g. Thereafter, LR6 type alkaline manganese battery B was manufactured according to a conventional method. Table 1 shows the time required for infiltration and the amount of electrolyte infiltrated in Batteries A and B manufactured as described above. Also, the internal resistance of batteries A and B and -10℃, 2Ω intermittent discharge (5 seconds discharge/5 seconds rest)
Table 2 shows the results of measuring the discharge time (net discharge time) to the final voltage of 0.9V.
【表】【table】
【表】
第1表および第2表に示すように、本発明の方
法により製造された電池Aは、電解液の浸潤に要
する時間が短く、かつ電池特性が優れている。
なお、実施例では多孔体としてのビニロンーレ
ーヨン混抄紙を正極合剤の中空部に挿入し、つい
でコアロツドを該ビニロンーレーヨン混抄紙より
なる筒状部の中空部に挿入したが、それによら
ず、多孔体をコアロツドに装着して、多孔体をコ
アロツドと一緒に正極合剤の中空部内に挿入して
もよい。また、実施例では多孔体は下部に底部を
設けたコツプ状の状態で正極合剤の中空部に挿入
したが、有底筒状のセパレータを用いる場合など
には、必ずしも底部を設けていなくてもよい。[Table] As shown in Tables 1 and 2, the battery A manufactured by the method of the present invention requires a short time for infiltration of the electrolyte and has excellent battery characteristics. In the example, vinylon-rayon mixed paper as a porous body was inserted into the hollow part of the positive electrode mixture, and then a core rod was inserted into the hollow part of the cylindrical part made of the vinylon-rayon mixed paper. Alternatively, the porous body may be attached to the core rod, and the porous body may be inserted into the hollow portion of the positive electrode mixture together with the core rod. In addition, in the example, the porous body was inserted into the hollow part of the positive electrode mixture in a pot-like state with a bottom provided at the bottom, but if a cylindrical separator with a bottom is used, the bottom may not necessarily be provided. Good too.
第1図〜第3図は本発明に係る筒形アルカリ電
池を示す図で、第1図および第2図は製造中の状
態を示す断面図、第3図は製造後の状態を示す部
分断面図である。第4図〜第5図は従来の筒形ア
ルカリ電池を示す図で、第4図は製造中の状態を
示す断面図、第5図は製造後の状態を示す部分断
面図である。
1……正極缶、2a……多孔体としてのビニロ
ンーレーヨン混抄紙よりなる筒状部、3……正極
合剤、4……セパレータ、21……コアロツド。
1 to 3 are views showing a cylindrical alkaline battery according to the present invention, FIGS. 1 and 2 are cross-sectional views showing the state during manufacture, and FIG. 3 is a partial cross-sectional view showing the state after manufacture. It is a diagram. 4 and 5 are views showing a conventional cylindrical alkaline battery, with FIG. 4 being a cross-sectional view showing the state during manufacture, and FIG. 5 being a partial cross-sectional view showing the state after manufacture. DESCRIPTION OF SYMBOLS 1... Positive electrode can, 2a... Cylindrical part made of vinylon-rayon mixed paper as a porous body, 3... Positive electrode mixture, 4... Separator, 21... Core rod.
Claims (1)
の内壁に沿つて積み重ね、該正極合剤の中空部に
保液性を有する多孔体およびコアロツドを挿入
し、正極合剤とコアロツドとの間に上記多孔体を
介在させた状態で正極合剤を上方から加圧して、
正極合剤を正極缶の内壁に圧着させた後、コアロ
ツドを引き抜き、上記多孔体が形成する筒状部の
中空部にセパレータを挿入することを特徴とする
筒形アルカリ電池の製造法。 2 多孔体およびセパレータの材質がビニロン−
レーヨン混抄紙である特許請求の範囲第1項記載
の筒形アルカリ電池の製造法。[Claims] 1. A plurality of ring-shaped positive electrode mixtures are stacked along the inner wall of a positive electrode can, a porous body and a core rod having liquid retention properties are inserted into the hollow part of the positive electrode mixture, and the positive electrode mixture is formed into a ring shape. Pressurizing the positive electrode mixture from above with the porous body interposed between the agent and the core rod,
A method for producing a cylindrical alkaline battery, which comprises pressing a positive electrode mixture onto the inner wall of a positive electrode can, pulling out the core rod, and inserting a separator into the hollow part of the cylindrical part formed by the porous body. 2 The material of the porous body and separator is vinylon.
A method for producing a cylindrical alkaline battery according to claim 1, which is made of rayon mixed paper.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58099215A JPS59224068A (en) | 1983-06-02 | 1983-06-02 | Manufacture of tubular alkali cell |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58099215A JPS59224068A (en) | 1983-06-02 | 1983-06-02 | Manufacture of tubular alkali cell |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59224068A JPS59224068A (en) | 1984-12-15 |
| JPH0465500B2 true JPH0465500B2 (en) | 1992-10-20 |
Family
ID=14241428
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58099215A Granted JPS59224068A (en) | 1983-06-02 | 1983-06-02 | Manufacture of tubular alkali cell |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59224068A (en) |
-
1983
- 1983-06-02 JP JP58099215A patent/JPS59224068A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59224068A (en) | 1984-12-15 |
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