JPS60258861A - Manufacture of alkaline battery - Google Patents

Manufacture of alkaline battery

Info

Publication number
JPS60258861A
JPS60258861A JP11586184A JP11586184A JPS60258861A JP S60258861 A JPS60258861 A JP S60258861A JP 11586184 A JP11586184 A JP 11586184A JP 11586184 A JP11586184 A JP 11586184A JP S60258861 A JPS60258861 A JP S60258861A
Authority
JP
Japan
Prior art keywords
electrolyte
zinc
negative electrode
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.)
Granted
Application number
JP11586184A
Other languages
Japanese (ja)
Other versions
JPH0452595B2 (en
Inventor
Osamu Takahashi
修 高橋
Katsunori Nakatani
勝則 中谷
Hitoshi Takagishi
高岸 仁
Kazutaka To
陶 和孝
Kiyoshi Hosoda
細田 清志
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.)
FDK Twicell Co Ltd
Original Assignee
Toshiba 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 Toshiba Battery Co Ltd filed Critical Toshiba Battery Co Ltd
Priority to JP11586184A priority Critical patent/JPS60258861A/en
Publication of JPS60258861A publication Critical patent/JPS60258861A/en
Publication of JPH0452595B2 publication Critical patent/JPH0452595B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/06Electrodes for primary cells
    • H01M4/08Processes of manufacture
    • H01M4/12Processes of manufacture of consumable metal or alloy electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00Primary cells; Manufacture thereof
    • H01M6/22Immobilising of electrolyte

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)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To obtain a battery with improved discharge performance under the condition of heavy load and low temperature by making a gel-like zinc negative electrode by pouring electrolyte containin a compound such as Na-di-n-octylsulfosuccinate into a mixture powder composed of amalgamated zinc and a pasty material. CONSTITUTION:After given amounts of an amalgamated zinc powder and a pasty material such as soda polyacrylate are packed into a sealing plate also serving as a negative terminal, alkaline electrolyte containing Na-di-n-octylsulphosuccinate or Na-dinonylnaphthalene sulfonate is poured into the packed materials, thereby making a gel-like zinc negative electrode. Then, an alkaline battery of the button type or similar type is assembled by using the thus made negative electrode. Since a surfactant is contained in the electrolyte of this alkaline battery, the evaporation of moisture from the electrolyte can be suppressed between the time of electrolyte pouring and the time when the negative electrode is attached to the positive electrode. Consequently, it is possible to equalize the quality of the zinc negative electrode.

Description

【発明の詳細な説明】 〔発明の技術分野〕 この発明は、ゲル状亜鉛陰極を改良したアルカリ電池の
製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] This invention relates to a method for manufacturing an alkaline battery using an improved gelled zinc cathode.

〔発明の技術的背景とその問題点〕[Technical background of the invention and its problems]

亜鉛粉末とアルカリ電解液と糊料とを混練して形成した
ゲル状亜鉛陰極を用いるアルカリ電池においては、従来
あらかじめゲル状にしたアルカリ電解液中に亜鉛粉末を
分散させることによりゲル状亜鉛陰極を得ていた。しか
し、このような手段で得る亜鉛陰極は秤取する際の精度
が低い欠点があった。
In alkaline batteries that use a gelled zinc cathode formed by kneading zinc powder, an alkaline electrolyte, and a glue, conventionally, the gelled zinc cathode is formed by dispersing zinc powder in an alkaline electrolyte that has been made into a gel beforehand. I was getting it. However, the zinc cathode obtained by such a method has a drawback of low accuracy in weighing.

そこで、最近では特開昭57−60660号や特開昭5
7−60661号に示すように、亜鉛粉末と糊料との混
合粉をまず秤取し、次にアルカリ電解液を注液してゲル
状亜鉛陰極を形成する方法が用いられるようになった。
Therefore, recently, Japanese Patent Application Publication No. 57-60660 and Japanese Patent Application Publication No. 5
As shown in No. 7-60661, a method has been used in which a mixed powder of zinc powder and a paste is first weighed, and then an alkaline electrolyte is poured into it to form a gelled zinc cathode.

しかしながら、混練していないゲル状亜鉛陰極は、亜鉛
粉末が均一に分散せずしかも亜鉛粉末表面が十分に濡れ
ず低活性きなっているため、特に放電初期の放電性能を
劣化させ不均一であったりさらには電池寿命を減少させ
る等の欠点があった。
However, in gelled zinc cathodes that are not kneaded, the zinc powder is not uniformly dispersed and the surface of the zinc powder is not sufficiently wetted, resulting in low activity, which deteriorates the discharge performance especially in the early stage of discharge and causes unevenness. Furthermore, there were drawbacks such as shortening of battery life.

〔発明の目的〕[Purpose of the invention]

この発明は上記の欠点を除去し、電池の重負荷および低
温での放電性能を向上し初期容量が大きいとともiこ貯
蔵寿命が長くしかも各性能を均一化させることのできる
アルカリ電池の製造方法を提供しようとするものである
This invention eliminates the above-mentioned drawbacks, improves the discharge performance of the battery under heavy loads and low temperatures, has a large initial capacity, has a long shelf life, and is a method for producing an alkaline battery that can make each performance uniform. This is what we are trying to provide.

〔発明の概要〕[Summary of the invention]

この発明は、アルカリ電池の製造に当り、汞化亜鉛と糊
量との混合粉を所定量秤取しこれにNa−ジ−ローオク
チルスルホクシネートもしくはN?ジノニルナフタレン
スルホネートを含むアルカリ電解液を注液して得た亜鉛
陰極を用いることを特徴としている。
In the production of alkaline batteries, the present invention involves weighing out a predetermined amount of a mixed powder of zinc chloride and an amount of glue, adding Na-zi-low octyl sulfocinate or N? It is characterized by the use of a zinc cathode obtained by injecting an alkaline electrolyte containing dinonylnaphthalene sulfonate.

〔発明の効果〕〔Effect of the invention〕

この発明において用いるゲル状亜鉛陰極は、アルカリ電
解液に界面活性剤であるNa−ジ−n−オクチルスルホ
サクシネートもしくはNa−ジノニルナフタレンスルホ
ネートをぎんでいるので、汞化亜鉛粉が均一かつ安定に
分散しかつ電解液との親和性が増し放電生成物の拡散を
助けることができる。
In the gelled zinc cathode used in this invention, the alkaline electrolyte contains surfactant Na-di-n-octyl sulfosuccinate or Na-dinonylnaphthalene sulfonate, so that the zinc chloride powder is uniform and stable. This increases the affinity with the electrolytic solution and helps the dispersion of discharge products.

したがって、゛電池の重負荷および低温での放電性能を
向上し初期容量を大きくすることができる。
Therefore, it is possible to improve the discharge performance of the battery under heavy loads and at low temperatures, and to increase the initial capacity.

また電解液が界面活性剤を含んでいるので、電解液の注
液から陽極部との嵌合までの間に、電解液の水分が空気
中に蒸発するのを抑えることかで1 き亜鉛陰極の品質
の均一化を計ることができる。
In addition, since the electrolyte contains a surfactant, the zinc cathode prevents moisture in the electrolyte from evaporating into the air between the time the electrolyte is poured and the anode is fitted. It is possible to measure the uniformity of quality.

々 したがって“電池の各性能を均一化し貯蔵役命を長期化
し得る特長がある。
Therefore, it has the advantage of equalizing each battery's performance and extending its storage life.

〔発明の実施例〕[Embodiments of the invention]

以下、図面を参照してこの発明の一実施例をボタン型ア
ルカリ電池の場合について説明する。
Hereinafter, an embodiment of the present invention will be described in the case of a button-type alkaline battery with reference to the drawings.

添付図面において、1は鉄にニッケルメッキを施した陽
極端子を兼ねる金属外装容器で、酸化銀(Ago、Ag
zO)もしくは二酸化マンガン(Mn02)を陽極活物
質とした合剤成形体2をその内壁lこ密着させて充填す
る。次に、合剤成形体2の上部にセパレータ3を配設す
る。このセパレータ3としては例えばQ、1mmの厚さ
の微孔性ポリエチレンの両面にセロファンを積層した構
成のものを用いる。
In the attached drawings, reference numeral 1 denotes a metal outer container that also serves as an anode terminal, which is made of nickel-plated iron, and contains silver oxide (Ago, Ag).
A mixture molded body 2 containing manganese dioxide (Mn02) or manganese dioxide (Mn02) as an anode active material is packed in close contact with the inner wall thereof. Next, a separator 3 is placed on top of the mixture molded body 2. This separator 3 is made of, for example, Q, a 1 mm thick microporous polyethylene layered with cellophane on both sides.

セパレータ3の上にレーヨンからなる不織布4を設け、
さらζこその上部にアルカリ電解液によるゲル状亜鉛陰
極5を配置する。6は内面に銅、外面にニッケルメッキ
を施した鉄板からなり陰極端子を兼ねる封目板で、その
周縁1こ絶縁バッキング7を嵌着し、金属外装容器1の
開口部8を内方へ折曲し締め付けることによiて電池を
完成する。
A nonwoven fabric 4 made of rayon is provided on the separator 3,
A gelled zinc cathode 5 made of an alkaline electrolyte is placed on top of the plate ζ. 6 is a sealing plate made of iron plated with copper on the inside and nickel on the outside, which also serves as a cathode terminal; an insulating backing 7 is fitted around its periphery, and the opening 8 of the metal outer container 1 is folded inward. Complete the battery by bending and tightening.

上記ゲル状亜鉛電極5は、例えば48〜100メツシニ
の10重量%氷化亜鉛粉100gと糊料であるポリアク
リル酸ソーダ粉5gを混合し、電池1個分に相当する所
定量を秤取して陰極端子を兼ねる封口板6に挿填し、N
a−ジーn−オクチルスルホサクシネートもしくはNa
−ジノニルナフタレンスルホネートを0.02重量%含
みかつ酸化亜鉛を溶解した26重計チの苛性ソーダ溶液
を注液して形成するものである。
The above-mentioned gelled zinc electrode 5 is made by mixing 100 g of 10% by weight frozen zinc powder of 48 to 100 methane and 5 g of sodium polyacrylate powder as a glue, and weighing out a predetermined amount equivalent to one battery. and insert it into the sealing plate 6 which also serves as a cathode terminal, and
a-Di-n-octyl sulfosuccinate or Na
- It is formed by pouring 26 g of caustic soda solution containing 0.02% by weight of dinonylnaphthalene sulfonate and dissolving zinc oxide.

このようにして得たこの発明によるボタン型酸化銀アル
カリ電池〔A〕と、界面活性剤を含まない同型電池の従
来品〔B〕との性能を比較すると次の通りである。
The performance of the thus obtained button-type silver oxide alkaline battery [A] according to the present invention and a conventional battery of the same type that does not contain a surfactant [B] is as follows.

第1表は−1012,2にΩ定抵抗放電5秒後の閉路電
圧をOチ、40チ、80チの放電深度別に示したもので
ある。また第2表は20℃、30にΩ定抵抗放電におけ
る1、2■までの持続時間を示している。さらに、第3
表は60℃で貯蔵した結果で(A〕(Bl ともに製造
直後を100%とし、20,40.60 日貯蔵後に2
0℃、30にΩで放電し、1.2Vになるまでの放電容
量の維持率〔チ〕を示したものである。なお、これらの
データを得るための試験電池の数は(A〕(Blともそ
れぞれ5個である。
Table 1 shows the closed-circuit voltage after 5 seconds of discharge with a constant resistance of -1012.2 Ω, according to the discharge depths of 0 inches, 40 inches, and 80 inches. Table 2 also shows the duration up to 1 and 2 ■ in constant resistance discharge at 20° C. and 30Ω. Furthermore, the third
The table shows the results of storage at 60℃ (A) (Bl Both are 100% immediately after manufacture, and 20% after storage for 20 and 40.60 days.
The figure shows the discharge capacity maintenance rate [chi] when discharged at 0°C and 30Ω until the voltage reached 1.2V. Note that the number of test batteries for obtaining these data was 5 each for (A) (Bl).

第 1 表 第 2 表 第 3 表 第1表ないし第3表から明らかなようにこの発明による
もの[A、]は従来品CB]に比して、閉路電圧、持続
時間、維持率のいずれにおいても著しく向上し、放電性
能および貯蔵性の優れたものであることが明らかである
Table 1 Table 2 Table 3 As is clear from Tables 1 to 3, the product according to the present invention [A] is superior to the conventional product CB in terms of closed circuit voltage, duration, and maintenance rate. It is clear that the discharge performance and storage property are excellent.

なお、この発明は上記実施例に限定されるものではなく
要旨を変更しない範囲において種々変形して実施するこ
とができる。
Note that the present invention is not limited to the above-mentioned embodiments, and can be implemented with various modifications without changing the gist.

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

添付図面は、この発明の一実施例によって得たボタン型
アルカリ電池の断面図である。 1・・・金属外装容器 2・・・陽極活物質3・・・セ
パレータ 4・・・不織布 5・・・ゲル状亜鉛陰極 6・・・封目板7・・・絶縁
バッキング 8・・・開口部出願人 東芝電池株式会社 4356 7 A 2 特許庁長官 志 賀 学 殿 特願昭59−115861号 2、発明の名称 アルカリ電池の製造方法 3、補正をする者 事件との関係特許出願人 (353)東芝電池株式会社 4代理人 6、補正の夕・1象 明細書 補正の内容 )本願明細書の第6頁目に記載の第1表を下記のように
訂正する。 記 第 1 表
The accompanying drawing is a sectional view of a button-type alkaline battery obtained according to an embodiment of the present invention. 1... Metal outer container 2... Anode active material 3... Separator 4... Nonwoven fabric 5... Gel-like zinc cathode 6... Sealing plate 7... Insulating backing 8... Opening Section Applicant: Toshiba Battery Corporation 4356 7 A 2 Commissioner of the Patent Office Manabu Shiga Patent Application No. 115861/1983 2 Title of Invention Process for Producing Alkaline Batteries 3 Patent Applicant Related to the Amendment Person Case (353 ) Toshiba Battery Co., Ltd. 4 Agent 6, Amendment 1 Contents of amendment to the specification) Table 1 stated on page 6 of the specification of the present application is corrected as follows. Table 1

Claims (1)

【特許請求の範囲】[Claims] 汞化亜鉛と糊料との混合粉を所定量秤取しこれにNa−
ジ−n−オクチルスルホサクシネートもしくはNa−ジ
ノニルナフタレンスルホネートを含むアルカリ電解液を
注液してゲル状亜鉛陰極を形成しこれを用いて電池を構
成することを特徴とするアルカリ電池の製造方法。
Weigh out a predetermined amount of mixed powder of zinc chloride and glue, and add Na-
A method for producing an alkaline battery, which comprises injecting an alkaline electrolyte containing di-n-octyl sulfosuccinate or Na-dinonylnaphthalene sulfonate to form a gelled zinc cathode, and using this to construct a battery. .
JP11586184A 1984-06-06 1984-06-06 Manufacture of alkaline battery Granted JPS60258861A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11586184A JPS60258861A (en) 1984-06-06 1984-06-06 Manufacture of alkaline battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11586184A JPS60258861A (en) 1984-06-06 1984-06-06 Manufacture of alkaline battery

Publications (2)

Publication Number Publication Date
JPS60258861A true JPS60258861A (en) 1985-12-20
JPH0452595B2 JPH0452595B2 (en) 1992-08-24

Family

ID=14672961

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11586184A Granted JPS60258861A (en) 1984-06-06 1984-06-06 Manufacture of alkaline battery

Country Status (1)

Country Link
JP (1) JPS60258861A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007515757A (en) * 2003-12-12 2007-06-14 エヴァレディ・バッテリー・カンパニー・インコーポレイテッド Electrochemical cell
CN108574085A (en) * 2018-03-22 2018-09-25 复旦大学 A kind of low temperature Zinc ion battery

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007515757A (en) * 2003-12-12 2007-06-14 エヴァレディ・バッテリー・カンパニー・インコーポレイテッド Electrochemical cell
CN108574085A (en) * 2018-03-22 2018-09-25 复旦大学 A kind of low temperature Zinc ion battery

Also Published As

Publication number Publication date
JPH0452595B2 (en) 1992-08-24

Similar Documents

Publication Publication Date Title
GB2028565A (en) Alkaline primary cells
JPH09106812A (en) Alkali manganese dioxide battery
JPS60258861A (en) Manufacture of alkaline battery
US2620368A (en) Alkaline dry cell
JPH048899B2 (en)
JPS5971259A (en) Alkaline storage battery and its manufacturing method
JPS58112254A (en) Alkaline cell
JPS6178057A (en) Method for manufacturing alkaline battery
JPH0452596B2 (en)
JPH0443387B2 (en)
JPS5978451A (en) Battery
JPH1173949A (en) Air zinc battery
JPS5854558A (en) Manufacture of alkaline battery
JPS58197675A (en) Alkaline cell
JPS6188452A (en) Button type alkaline cell
JP3086313B2 (en) Manganese dry cell
JPS58216360A (en) Manufacture of silver oxide battery
JPS5866269A (en) Alkaline battery
JPS61176060A (en) Button-shaped alkaline cell
JPH0244105B2 (en) HISUIYOBAIDENCHI
JPS62136770A (en) Alkaline battery
JPS6362868B2 (en)
JPS62123659A (en) Organic electrolyte battery
JPS61185864A (en) Silver oxide cell
JPS585965A (en) Alkaline battery