JPS5942949B2 - nickel electrode - Google Patents

nickel electrode

Info

Publication number
JPS5942949B2
JPS5942949B2 JP51150494A JP15049476A JPS5942949B2 JP S5942949 B2 JPS5942949 B2 JP S5942949B2 JP 51150494 A JP51150494 A JP 51150494A JP 15049476 A JP15049476 A JP 15049476A JP S5942949 B2 JPS5942949 B2 JP S5942949B2
Authority
JP
Japan
Prior art keywords
nickel
binder
electrode
polystyrene
nickel 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.)
Expired
Application number
JP51150494A
Other languages
Japanese (ja)
Other versions
JPS5374247A (en
Inventor
輝雄 山根
博資 山崎
泰之 熊野
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP51150494A priority Critical patent/JPS5942949B2/en
Publication of JPS5374247A publication Critical patent/JPS5374247A/en
Publication of JPS5942949B2 publication Critical patent/JPS5942949B2/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

Description

【発明の詳細な説明】 本発明はニッケル−カドミウム、ニッケル−亜鉛蓄電池
などに用いるニッケル電極の改良に関するもので、その
目的は低コストで、しかも実用上好ましい性質の電極を
提供することにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvements in nickel electrodes used in nickel-cadmium, nickel-zinc storage batteries, etc., and its purpose is to provide electrodes that are low in cost and have practically desirable properties.

従来ニッケル電極は、ニッケル粉末を焼結した多孔度7
5〜85%の基板を用い、これを濃度調節した硝酸ニッ
ケル溶液に浸漬し、後熱分解して活物質とする方法で製
造されていた。この方法によつて得られた電極は良好な
性能を有しており、高率放電にも強く、しかも長寿命で
ある特長を持つている。しカルながら上記焼結式ニッケ
ル電極にはコストが高い欠点があつた。その原因は基板
を得るために高温還元雰囲気で焼結すること、活物質充
填工程を多数回繰り返す、などから設備費、光熱費、人
件費を多く要することにあつた。最近、焼結式電極の長
所を可及的に維持しながらコストの安いニッケル電極を
得る目的で、活物質と導電材と合成樹脂結着剤などを、
それぞれ適量混合してペースト状とし、ニッケルパンチ
ングメタルなどからなる集電体に塗着、乾燥して加圧と
同時に加熱するか、加圧成形後適当な温度で加熱し、極
板とする方法が注目されている。なかでも結着剤として
ポリスチレンを用いたものが耐アルカリ性が良好でサイ
クル寿命も優れていることが知られている。例えば水酸
化ニッケル70重量%に鱗状黒鉛15重量%とポリスチ
レン粉末10重量%および酸化コバルト5重量%を秤取
し、これに適量の水を加えてよく混合し、ペースト状と
したものをニッケルパンチングメタルの集電体の両面に
塗着し、乾燥後加圧成形して更に150℃に加熱し、ニ
ッケル電極を得ていた。
Conventional nickel electrodes are made of sintered nickel powder with a porosity of 7.
The active material was produced by using a 5-85% substrate, immersing it in a nickel nitrate solution with an adjusted concentration, and then thermally decomposing it. The electrode obtained by this method has good performance, is resistant to high rate discharge, and has a long life. However, the above sintered nickel electrode had the disadvantage of high cost. The reason for this is that in order to obtain the substrate, sintering is performed in a high-temperature reducing atmosphere, and the process of filling the active material is repeated many times, resulting in high equipment costs, utility costs, and personnel costs. Recently, in order to obtain a low-cost nickel electrode while maintaining the advantages of sintered electrodes as much as possible, active materials, conductive materials, synthetic resin binders, etc.
Mix appropriate amounts of each to make a paste, apply it to a current collector made of nickel punching metal, dry it, and heat it at the same time as pressurizing it, or heat it at an appropriate temperature after pressure molding to make an electrode plate. Attention has been paid. Among these, those using polystyrene as a binder are known to have good alkali resistance and cycle life. For example, weigh out 70% by weight of nickel hydroxide, 15% by weight of scale graphite, 10% by weight of polystyrene powder, and 5% by weight of cobalt oxide, add an appropriate amount of water, mix well, make a paste, and then nickel punch. It was applied to both sides of a metal current collector, dried, pressure-molded, and further heated to 150°C to obtain a nickel electrode.

この極板は先にも述べた通リサイクル寿命は優れている
が、得られた極板が柔軟性に乏しく、渦巻状にして用い
た場合、クラックに伴う活物質の脱落現象が多く認めら
れる欠点があつた。本発明の目的は先に述べた通り、活
物質と導電材と結着剤を主体とした混合物を集電体に加
圧成形して得るニッケル電極の改良に係るもので、低コ
ストで取扱中の脱落がない実用的な電極を提供すること
にある。
This electrode plate has an excellent recycling life as mentioned above, but the drawback is that the obtained electrode plate lacks flexibility, and when used in a spiral shape, the active material often falls off due to cracks. It was hot. As stated above, the purpose of the present invention is to improve a nickel electrode obtained by press-molding a mixture mainly consisting of an active material, a conductive material, and a binder into a current collector, and is available at a low cost. The objective is to provide a practical electrode that does not fall off.

本発明の実施例を円筒形ニツケルーカドミウム蓄電池の
図面とともに説明する。
Embodiments of the present invention will be described with reference to drawings of a cylindrical nickel-cadmium storage battery.

図は全体構成の概要を示す縦断面図である。1は負極板
で酸化カドミウムを主体とした混合物をニツケル集電体
に塗着し、乾燥後プレスしたペースト式極板、2はセパ
レータでポリアミド不織布からなり、負極1と正極3の
間に介在し、正・負極板の端部より1〜 3mm突出し
た構造になつている。
The figure is a longitudinal sectional view showing an outline of the overall configuration. 1 is a negative electrode plate, which is a paste-type electrode plate in which a mixture mainly composed of cadmium oxide is applied to a nickel current collector, dried, and then pressed; 2 is a separator, which is made of polyamide nonwoven fabric, and is interposed between negative electrode 1 and positive electrode 3. The structure is such that it protrudes 1 to 3 mm from the ends of the positive and negative electrode plates.

3は本発明の正極で活物貨、導電材、結着剤を主体とす
る混合物をニツケルパンチングメタル集電体の両面に塗
着、乾燥後加圧成形して熱処理したもので、従来と異な
る点は結着剤としてポリスチレンにエチレン一酢酸ビニ
ル共重合樹脂粉末またはスチレンーブタジエンラテツク
スを併用したことにある。
3 is the positive electrode of the present invention, in which a mixture mainly consisting of a live substance, a conductive material, and a binder is applied to both sides of a nickel punched metal current collector, dried, and then pressure-molded and heat-treated, which is different from the conventional one. The key point is that ethylene monovinyl acetate copolymer resin powder or styrene-butadiene latex is used in combination with polystyrene as a binder.

4は正極板3のリードで絶縁チユーブで保護してあ〔り
、封口板5にスポツト溶接にて電気導通し、封口板5が
正極端子になるように設計されている。
4 is a lead of the positive electrode plate 3, which is protected by an insulating tube, and is electrically connected to a sealing plate 5 by spot welding, so that the sealing plate 5 becomes a positive terminal.

6は負極のリードであり、その端部を外装缶1の内面に
スポツト溶接することで外装缶Tが負極端子になつてい
る。
Reference numeral 6 denotes a negative electrode lead, and by spot welding its end to the inner surface of the outer can 1, the outer can T becomes a negative electrode terminal.

8は下部絶縁板、9は上部絶縁板で正極リード4が通る
穴が設けられている。
8 is a lower insulating plate, and 9 is an upper insulating plate, each having a hole through which the positive electrode lead 4 passes.

なお電解液は7Nの水酸化カリウム水溶液を用いた。電
池構成は以上の如くであるが、本発明の特徴は正極合剤
の活物質、導電材、結着剤を主体とした混合物の結着剤
にあり、実施例によつて更に詳しくその製法を説明する
。固形分の重量比が第1表の処方になるように水酸化ニ
ツケル、鱗状黒鉛、結着剤、酸化コバルトを秤取し、こ
れに適量の水を加えてよく混練し、正極合剤ぺーストを
得る。このペーストを厚味0.1771771のニツケ
ルパンチングメタルの芯材の両面に塗着し、約80℃で
30〜60分間乾燥した後、乾燥後の厚味の60〜65
%になるような条件で加圧成形する。これを更に140
〜180℃で60分間熱処理してニツケル電極を得る。
このようにして得た本発明の電極を用いて先に述べた構
成にて円筒形電池を試作した。
Note that a 7N aqueous potassium hydroxide solution was used as the electrolyte. Although the battery configuration is as described above, the feature of the present invention is the binder, which is a mixture mainly consisting of an active material, a conductive material, and a binder for the positive electrode mixture. explain. Weigh out nickel hydroxide, graphite scales, binder, and cobalt oxide so that the solid content weight ratio is as shown in Table 1, add an appropriate amount of water, and mix thoroughly to form a positive electrode mixture paste. get. Apply this paste to both sides of the core material of nickel punching metal with a thickness of 0.1771771, and dry it at about 80°C for 30 to 60 minutes.
%. Add this to 140 more
A nickel electrode is obtained by heat treatment at ~180°C for 60 minutes.
Using the thus obtained electrode of the present invention, a cylindrical battery was prototyped with the configuration described above.

この時のニツケル電極の歩留およびサイクル寿命、価格
比について焼結式並に従来のポリスチレンのみを結着剤
とした加圧式と比較して第2表に示す。従来の欠点は、
焼結式についてはコストが高いことであり、活物質と導
電材その他をポリスレンを結着剤として加圧成形して得
る電極においては、サイクル寿命が優れている反面、柔
軟性に乏しく、電池組立の際の渦巻作業において折れた
り、著しいクラツクに伴う活物質の脱落が発生し、歩留
が悪い欠点であつた。本発明は低コストで、しかも歩留
のよい電極の提供を可能にしたものである。
Table 2 shows the yield, cycle life, and price ratio of the nickel electrode in comparison with the sintering method and the conventional pressurizing method using only polystyrene as a binder. The disadvantages of conventional
The cost of sintering is high, and electrodes obtained by pressure-molding the active material, conductive material, and other materials using polystyrene as a binder have excellent cycle life, but lack flexibility and are difficult to assemble. During the swirling process during the process, the active material may break or fall off due to severe cracking, resulting in poor yield. The present invention makes it possible to provide an electrode at low cost and with good yield.

即ち、第2表に示す如く、コストについては従来の焼結
式の約Xである。寿命については焼結式には及ばないも
のの、エチレン一酢酸ビニル共重合物またはエチレン−
ブタジエン共重合体の添加量を適当に選択することによ
つて、ポリスチレンのみを用いた場合に比較して遜色な
く、しかも歩留が大巾に改善される。歩留が改善された
理由は、エチレン一酢酸ビニル共重合物およびスチレン
−ブタジエン共重合体が柔軟性に富むため、ポリスチレ
ン単独では不足していた柔軟性を付与したためと思われ
る。但し、エチレン一酢酸ビニル共重合樹脂またはスチ
レン−ブタジエン共重合体量の添加量が過多になると寿
命は劣化するので量の規制を要する。なお、第2表の歩
留、サイクル寿命から判断してポリスチレンリエチレン
一酢酸ビニル共重合体の場合の適正比率は重量比で6:
4〜4:6、ポリスチレンリスチレンーブタジエン共重
合体の場合は9:1〜7:3の範囲である。本発明に用
いるエチレン一酢酸ビニル共重合樹脂は、酢酸ビニルの
含有量が4.5〜14重量%、スチレン−ブタジエン共
重合体はブタジエンの含有量が40〜70重量%の範囲
で同様の効果があつた。
That is, as shown in Table 2, the cost is about X compared to the conventional sintering method. Although it is not as long as the sintered type in terms of lifespan, ethylene monovinyl acetate copolymer or ethylene-vinyl acetate
By appropriately selecting the amount of the butadiene copolymer added, the yield can be improved significantly while being comparable to the case where only polystyrene is used. The reason for the improvement in yield is thought to be that the ethylene monovinyl acetate copolymer and the styrene-butadiene copolymer are highly flexible, providing flexibility that polystyrene alone lacks. However, if the amount of ethylene monovinyl acetate copolymer resin or styrene-butadiene copolymer added is too large, the life will deteriorate, so the amount must be regulated. Furthermore, judging from the yield and cycle life in Table 2, the appropriate ratio in the case of polystyrene lyethylene monovinyl acetate copolymer is 6:
The ratio is in the range of 4 to 4:6, and in the case of polystyrene-restyrene-butadiene copolymer, it is in the range of 9:1 to 7:3. The ethylene monovinyl acetate copolymer resin used in the present invention has a vinyl acetate content of 4.5 to 14% by weight, and the styrene-butadiene copolymer has a butadiene content of 40 to 70% by weight to achieve similar effects. It was hot.

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

図面は本発明の実施例を示すニツケルーカドミウム蓄電
池の縦断面図である。 1・・・・・・負極、2・・・・・・セパレータ、3・
・・・・・正極。
The drawing is a longitudinal sectional view of a Nickel-cadmium storage battery showing an embodiment of the present invention. 1... Negative electrode, 2... Separator, 3...
...Positive electrode.

Claims (1)

【特許請求の範囲】 1 ニッケル化合物からなる活物質と導電材と結着剤を
主体とする電極であつて、前記結着剤にエチレン−酢酸
ビニル共重合体及びスチレン−ブタジエン共重合体より
なる群から選んだ1種とポリスチレンとを併用したこと
を特徴とするニッケル電極。 2 結着剤のポリスチレンとエチレン−酢酸ビニル共重
合体の割合が重量比で6:4〜4:6である特許請求の
範囲第1項記載のニッケル電極。 3 結着剤のポリスチレンとスチレン−ブタジエン共重
合体の割合が重量比で9:1〜7:3である特許請求の
範囲第1項記載のニッケル電極。
[Scope of Claims] 1. An electrode mainly composed of an active material made of a nickel compound, a conductive material, and a binder, the binder being made of an ethylene-vinyl acetate copolymer and a styrene-butadiene copolymer. A nickel electrode characterized by the combination of one type selected from the group and polystyrene. 2. The nickel electrode according to claim 1, wherein the weight ratio of polystyrene and ethylene-vinyl acetate copolymer as a binder is 6:4 to 4:6. 3. The nickel electrode according to claim 1, wherein the weight ratio of polystyrene and styrene-butadiene copolymer as the binder is 9:1 to 7:3.
JP51150494A 1976-12-14 1976-12-14 nickel electrode Expired JPS5942949B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP51150494A JPS5942949B2 (en) 1976-12-14 1976-12-14 nickel electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP51150494A JPS5942949B2 (en) 1976-12-14 1976-12-14 nickel electrode

Publications (2)

Publication Number Publication Date
JPS5374247A JPS5374247A (en) 1978-07-01
JPS5942949B2 true JPS5942949B2 (en) 1984-10-18

Family

ID=15498084

Family Applications (1)

Application Number Title Priority Date Filing Date
JP51150494A Expired JPS5942949B2 (en) 1976-12-14 1976-12-14 nickel electrode

Country Status (1)

Country Link
JP (1) JPS5942949B2 (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4552821A (en) * 1983-06-30 1985-11-12 Duracell Inc. Sealed nickel-zinc battery
CN1144306C (en) * 1998-06-09 2004-03-31 松下电器产业株式会社 Negative electrode for secondary cell, negative plate for secondry cell, and secondary cell comprising the same
FR2824187B1 (en) * 2001-04-30 2006-08-04 Cit Alcatel NON-SINTERED ELECTRODE WITH NICKEL
FR2899018B1 (en) 2006-03-21 2008-05-23 Accumulateurs Fixes PLASTICATED ELECTRODE FOR ALKALINE ACCUMULATOR
FR2906083B1 (en) * 2006-09-15 2010-10-29 Accumulateurs Fixes PLASTICATED ELECTRODE FOR ALKALINE ACCUMULATOR.
FR2945892B1 (en) 2009-05-19 2011-09-02 Saft Groupe Sa PLASTICATED ELECTRODE FOR ALKALINE ACCUMULATOR

Also Published As

Publication number Publication date
JPS5374247A (en) 1978-07-01

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