JPH0757731A - Alkaline battery - Google Patents

Alkaline battery

Info

Publication number
JPH0757731A
JPH0757731A JP5225067A JP22506793A JPH0757731A JP H0757731 A JPH0757731 A JP H0757731A JP 5225067 A JP5225067 A JP 5225067A JP 22506793 A JP22506793 A JP 22506793A JP H0757731 A JPH0757731 A JP H0757731A
Authority
JP
Japan
Prior art keywords
negative electrode
gel
electrode active
active substance
positive electrode
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
JP5225067A
Other languages
Japanese (ja)
Other versions
JP3002362B2 (en
Inventor
Naomi Ishihara
直美 石原
Masao Kawaguchi
正夫 川口
Masatomo Oohashi
真智 大橋
Hitoshi Takagishi
仁 高岸
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 JP5225067A priority Critical patent/JP3002362B2/en
Publication of JPH0757731A publication Critical patent/JPH0757731A/en
Application granted granted Critical
Publication of JP3002362B2 publication Critical patent/JP3002362B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To stabilize discharge capacity by preventing clogging of a nozzle of a gel filling machine by using an almost spherical mercury-less zinc particle as a gel-like negative electrode active substance, and reducing dispersion of a filling quantity. CONSTITUTION:A ratio of a long diameter to a short diameter of a zinc powder particle and the particle size are selected in a prescribed range. This is mixed in alkaline aqueous solution, and a gel-like negative electrode active substance 3 is created. A positive electrode 1 is filled in a positive electrode case 2, and a separator 5 and an electrolyte holding material 6 are placed on an upper surface. An insulating packing 7 is fitted around a sealing plate 4, and the negative electrode active substance 3 obtained by mixing an almost spherical Zn powder particle 8 and gel-like electrolyte 9 together, is filled by equivalency inside of the sealing plate 4 by a gel filling machine. A positive electrode body and a negative electrode body are fitted to/combined with each other, and the upper end of the positive electrode case is bent inside and is sealed. In this constitution, clogging of a filling nozzle is not caused, and weight dispersion of the filled negative electrode active substance is reduced, and dispersion of discharge maintaining time is also reduced, and a stable-quality battery can be obtained.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はアルカリ電池の負極作用
物質の改良に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to improvement of a negative electrode active material for alkaline batteries.

【0002】[0002]

【従来の技術】近年になって、亜鉛粉末に鉛、アルミニ
ウム、インジウム、ガリウム、カルシウムのうち少なく
とも一種以上含有する亜鉛粉粒子を使用することによ
り、水銀を添加しなくても、負極作用物質として電池に
組み込むことが可能となってきた。しかしながら汞化亜
鉛の場合は汞化の過程で亜鉛粉粒子の角がとれるが、無
汞化亜鉛の場合は粒子は原粉の針状のままの形状を維持
しており、図2のように、この針状の無汞化亜鉛粉粒子
18を、所定量のポリアクリル酸及び酸化亜鉛を溶解し
た所定濃度のアルカリ水溶液19に混合し、ゲル状とし
たものを負極作用物質13として電池に充填していた。
2. Description of the Related Art In recent years, by using zinc powder particles containing at least one of lead, aluminum, indium, gallium, and calcium in zinc powder, it is possible to obtain a negative electrode acting substance without adding mercury. It has become possible to incorporate it in batteries. However, in the case of zinc fluoridation, the particles of the zinc powder are sharpened in the process of hydration, but in the case of unfluorinated zinc, the particles maintain the needle-like shape of the raw powder, as shown in Fig. 2. The needle-shaped unremoved zinc powder particles 18 are mixed with an alkaline aqueous solution 19 having a predetermined concentration in which a predetermined amount of polyacrylic acid and zinc oxide are dissolved, and the gel-like substance is charged into the battery as the negative electrode active substance 13. Was.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、従来は
無汞化亜鉛の粒子形状が針状のままであるため、亜鉛粒
子同士の摩擦が大きく流動性が乏しい。このためゲル状
とした負極作用物質を電池に充填する際、充填ノズルの
先端で粒子同士の架橋状態が起こり、ノズルがつまり易
いという不具合が生じた。また、充填された負極作用物
質も重量のバラツキが大きく、結果的に、使用時におい
て放電持続時間のバラツキも大きくなってしまうという
問題点があった。
However, conventionally, since the particle shape of the unconstrained zinc remains acicular, the friction between zinc particles is large and the fluidity is poor. For this reason, when the battery is filled with the gelled negative electrode active substance, particles are cross-linked at the tip of the filling nozzle, which causes a problem that the nozzle is easily clogged. Further, the filled negative electrode active material also has a large variation in weight, resulting in a large variation in discharge duration during use.

【0004】本発明は無汞化亜鉛粉粒子の形状がほぼ球
状のものを使用することにより、所定量のポリアクリル
酸及び酸化亜鉛を溶解した所定濃度のアルカリ水溶液に
混合し、ゲル状としたものをゲル充填機で電池に組み込
む際、亜鉛粒子の摩擦が軽減され、流動性も良好とな
り、ノズルの先端でのつまり等の不具合がなく、また放
電持続時間のバラツキも少ない安定した品質のアルカリ
電池を提供することを目的とする。
According to the present invention, by using the non-defining zinc powder particles having a substantially spherical shape, a predetermined amount of polyacrylic acid and zinc oxide are mixed with an alkaline aqueous solution of a predetermined concentration to form a gel. When assembling things into a battery with a gel filling machine, friction of zinc particles is reduced, fluidity is also good, there is no problem such as clogging at the tip of the nozzle, and there is little variation in discharge duration time. The purpose is to provide a battery.

【0005】[0005]

【課題を解決するための手段】このような問題点を解決
するために、本発明は亜鉛粉末に鉛、アルミニウム、イ
ンジウム、ビスマス、ガリウム、カルシウムのうち少な
くとも一種以上含有する無汞化の亜鉛粉粒子の形状がほ
ぼ球状であるものを電池に組み込むものである。詳しく
は、本発明は前記亜鉛粉粒子の長直径/短直径比が1.
0〜2.0であり、かつ粒度分布が40〜150mes
hに分級したものを負極作用物質として用いるアルカリ
電池である。
In order to solve such problems, the present invention provides a zinc powder which contains at least one of lead, aluminum, indium, bismuth, gallium and calcium. The particles having a substantially spherical shape are incorporated in a battery. Specifically, in the present invention, the ratio of major diameter / minor diameter of the zinc powder particles is 1.
0 to 2.0 and particle size distribution of 40 to 150 mes
It is an alkaline battery that uses a substance classified into h as a negative electrode acting substance.

【0006】[0006]

【作用】前述したように、無汞化亜鉛粉粒子の形状がほ
ぼ球状のものを使用することにより、粒子間の摩擦を軽
減することができ、ゲル状とした負極作用物質を、負極
端子を兼ねる封口板に充填する際、充填ノズルの先端で
ゲルがつまるという不具合が起こらなくなった。また充
填された負極作用物質も重量のバラツキが少なく、放電
持続時間のバラツキも小さい安定した品質の電池を供給
することができる。
As described above, by using the non-alloyed zinc powder particles having a substantially spherical shape, the friction between the particles can be reduced, and the gelled negative electrode active material can be used as a negative electrode terminal. When filling the double-sided sealing plate, the problem that the gel is clogged at the tip of the filling nozzle no longer occurs. Further, the filled negative electrode active material has little variation in weight, and it is possible to supply a battery of stable quality with little variation in discharge duration.

【0007】また、前記球状亜鉛が、その粒子の長直径
/短直径比1.0〜2.0としたのは、2.0を越える
と、ゲル充填機のノズルの先端でのゲルづまりが完全に
解決されないためであり、粒度分布を40〜150me
shとしたのは、40mesh以下だと、粒子が大きい
ためゲルの重量バラツキにおいて充分な効果が得られ
ず、150mesh以上だと、粒子が細かすぎて粒子同
士の摩擦が大きくなり、ノズルの先端でゲルづまりを起
こすという問題が生じるからである。
The spherical zinc has a particle major diameter / minor diameter ratio of 1.0 to 2.0. When the ratio exceeds 2.0, gel clogging at the tip of the nozzle of the gel filling machine is complete. This is because the particle size distribution is 40 to 150 me.
If sh is 40 mesh or less, the particles are large, and therefore, sufficient effect cannot be obtained in weight variation of the gel. This is because the problem of gel clogging occurs.

【0008】[0008]

【実施例】本発明品と比較品とを説明する。亜鉛粉粒子
の長直径/短直径の比が、1.0,2.0,3.0で、
粒度が80〜120meshのものを作成した。それら
をポリアクリル酸および酸化亜鉛を溶解した所定濃度の
アルカリ水溶液に混合し、図1に示すゲル状の負極作用
物質3を作成した。これをゲル充填機を用いて5000
回運転しノズルづまりと、1000回ごとにn=10の
ゲル充填量を測定した。この充填機を用いて同時にSR
1130W型アルカリ電池を試作し放電した。また比較
のため、針状で上記比が5〜7である亜鉛粉粒子18を
用いて図2の負極作用物質13を作成し、同じ実験を行
ない結果を表1に示した。
EXAMPLES The invention product and the comparative product will be described. The ratio of major diameter / minor diameter of zinc powder particles is 1.0, 2.0, 3.0,
A particle size of 80 to 120 mesh was prepared. These were mixed with an alkaline aqueous solution having a predetermined concentration in which polyacrylic acid and zinc oxide were dissolved to prepare a gelled negative electrode active substance 3 shown in FIG. This is 5,000 using a gel filling machine.
The nozzle was clogged once, and the gel filling amount of n = 10 was measured every 1000 times. SR at the same time using this filling machine
A 1130 W alkaline battery was prototyped and discharged. For comparison, a negative electrode active material 13 of FIG. 2 was prepared using needle-shaped zinc powder particles 18 having the above ratio of 5 to 7, and the same experiment was performed. The results are shown in Table 1.

【0009】SR1130W型アルカリ電池は図3のよ
うに、まず正極ケース2内に正極1を充填し、その上面
にセパレータ5と電解液保持材6を載せる。一方封口板
4の周辺に絶縁パッキン7を嵌合し、封口板4の内部に
ほぼ球状の亜鉛粉粒子8とゲル状電解液9とが混合され
てなる図1の負極作用物質3をゲル充填機により等量充
填する。これら正極体と負極体とを嵌合して組合せ、正
極ケースの上端を内方へ折曲して封口してなっている。
これらのアルカリ電池を放電して容量を測定した。
As shown in FIG. 3, in the SR1130W alkaline battery, the positive electrode case 2 is first filled with the positive electrode 1, and the separator 5 and the electrolytic solution holding material 6 are placed on the upper surface thereof. On the other hand, an insulating packing 7 is fitted around the sealing plate 4, and the negative electrode active substance 3 of FIG. 1 obtained by mixing the spherical zinc powder particles 8 and the gel electrolyte 9 inside the sealing plate 4 is gel-filled. Fill equal amount by machine. The positive electrode body and the negative electrode body are fitted and combined with each other, and the upper end of the positive electrode case is bent inward and sealed.
These alkaline batteries were discharged and the capacity was measured.

【0010】[0010]

【表1】 [Table 1]

【0011】さらに最適な粒度分布を知るために、亜鉛
粒子の長直径/短直径が1.0,2.0のものについ
て、それぞれ粒度分布が、〜40mesh、40〜80
mesh、80〜120mesh、120〜150me
sh、150mesh〜のものについて、同じ実験を行
った。その結果を表2に示す。
In order to know the optimum particle size distribution, the particle size distributions of zinc particles having major and minor diameters of 1.0 and 2.0 are -40 mesh and 40-80, respectively.
mesh, 80-120 mesh, 120-150me
The same experiment was performed for sh, 150 mesh-. The results are shown in Table 2.

【0012】[0012]

【表2】 [Table 2]

【0013】表1,2のように、亜鉛粒子の長直径/短
直径の比が1.0〜2.0のものを使用すると、ゲル充
填機のノズル先端でのゲルづまりが全く起こらず、また
粒度分布については40〜150meshに分級したも
のを使用することにより、電池の容量バラツキも減らす
ことが可能である。
As shown in Tables 1 and 2, when zinc particles having a major diameter / minor diameter ratio of 1.0 to 2.0 are used, gel clogging does not occur at the nozzle tip of the gel filling machine, and Regarding the particle size distribution, it is possible to reduce the variation in the capacity of the battery by using the one classified into 40 to 150 mesh.

【0014】[0014]

【発明の効果】本発明は無汞化亜鉛粉末の粒子を、長直
径/短直径の比が1.0〜2.0であり、かつ粒度分布
が40〜150meshにすることにより、ゲル充填機
のノズルのつまりを防止し、負極作用物質の充填量を均
一にし、放電容量のバラツキの小さいアルカリ電池を得
ることができる。
EFFECTS OF THE INVENTION According to the present invention, the gel-filling machine is provided by making the particles of the unremoved zinc powder have a major diameter / minor diameter ratio of 1.0 to 2.0 and a particle size distribution of 40 to 150 mesh. It is possible to prevent the nozzle from being clogged, make the filling amount of the negative electrode active material uniform, and obtain an alkaline battery with a small variation in discharge capacity.

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

【図1】本発明によりなるほぼ球状亜鉛粉粒子を用いた
ゲル状負極作用物質の拡大図である。
FIG. 1 is an enlarged view of a gelled negative electrode active material using substantially spherical zinc powder particles according to the present invention.

【図2】従来の比較品の針状亜鉛粉粒子を用いたゲル状
負極作用物質の拡大図である。
FIG. 2 is an enlarged view of a gelled negative electrode active substance using conventional acicular zinc powder particles as a comparative product.

【図3】本発明のゲル状負極作用物質を用いたアルカリ
電池の断面図である。
FIG. 3 is a cross-sectional view of an alkaline battery using the gelled negative electrode active material of the present invention.

【符号の説明】[Explanation of symbols]

3 負極作用物質 8 亜鉛粉粒子 9 ゲル状電解液 18 亜鉛粉粒子 3 Negative Electrode Working Material 8 Zinc Powder Particles 9 Gel Electrolyte 18 Zinc Powder Particles

───────────────────────────────────────────────────── フロントページの続き (72)発明者 高岸 仁 東京都品川区南品川3丁目4番10号 東芝 電池株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hitoshi Takagishi 3-4-10 Minami-Shinagawa, Shinagawa-ku, Tokyo Inside Toshiba Battery Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 鉛、アルミニウム、インジウム、ビスマ
ス、ガリウム、カルシウムのうち少なくとも一種以上含
有する無汞化の亜鉛粉粒子を負極作用物質に用いるアル
カリ電池において、該亜鉛粉粒子の長直径/短直径の比
が、1.0〜2.0であり、かつ粉粒度分布が、40〜
150meshであることを特徴とするアルカリ電池。
1. In an alkaline battery in which unhydrogenated zinc powder particles containing at least one or more of lead, aluminum, indium, bismuth, gallium, and calcium are used as a negative electrode active material, the long diameter / short diameter of the zinc powder particles. Is 1.0 to 2.0, and the powder particle size distribution is 40 to
Alkaline battery characterized by being 150 mesh.
JP5225067A 1993-08-19 1993-08-19 Alkaline battery Expired - Fee Related JP3002362B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5225067A JP3002362B2 (en) 1993-08-19 1993-08-19 Alkaline battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5225067A JP3002362B2 (en) 1993-08-19 1993-08-19 Alkaline battery

Publications (2)

Publication Number Publication Date
JPH0757731A true JPH0757731A (en) 1995-03-03
JP3002362B2 JP3002362B2 (en) 2000-01-24

Family

ID=16823521

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5225067A Expired - Fee Related JP3002362B2 (en) 1993-08-19 1993-08-19 Alkaline battery

Country Status (1)

Country Link
JP (1) JP3002362B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006228503A (en) * 2005-02-16 2006-08-31 Sony Corp Alkaline battery
JP2007299622A (en) * 2006-04-28 2007-11-15 Fdk Energy Co Ltd Zinc powder for alkaline battery, negative electrode gel and alkaline battery
CN112072164A (en) * 2020-08-28 2020-12-11 蜂巢能源科技有限公司 Solid-state lithium battery and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006228503A (en) * 2005-02-16 2006-08-31 Sony Corp Alkaline battery
JP2007299622A (en) * 2006-04-28 2007-11-15 Fdk Energy Co Ltd Zinc powder for alkaline battery, negative electrode gel and alkaline battery
CN112072164A (en) * 2020-08-28 2020-12-11 蜂巢能源科技有限公司 Solid-state lithium battery and preparation method thereof

Also Published As

Publication number Publication date
JP3002362B2 (en) 2000-01-24

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