JPS61203559A - Manufacture of alkaline storage battery - Google Patents

Manufacture of alkaline storage battery

Info

Publication number
JPS61203559A
JPS61203559A JP60045556A JP4555685A JPS61203559A JP S61203559 A JPS61203559 A JP S61203559A JP 60045556 A JP60045556 A JP 60045556A JP 4555685 A JP4555685 A JP 4555685A JP S61203559 A JPS61203559 A JP S61203559A
Authority
JP
Japan
Prior art keywords
water
cadmium
active material
electrode
storage battery
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
Application number
JP60045556A
Other languages
Japanese (ja)
Inventor
Yoshiro Fujita
藤田 好郎
Nobuhisa Ueda
植田 信久
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.)
Japan Storage Battery Co Ltd
Original Assignee
Japan Storage 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 Japan Storage Battery Co Ltd filed Critical Japan Storage Battery Co Ltd
Priority to JP60045556A priority Critical patent/JPS61203559A/en
Publication of JPS61203559A publication Critical patent/JPS61203559A/en
Pending 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
    • H01M4/24Electrodes for alkaline accumulators
    • H01M4/26Processes of manufacture
    • 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

Abstract

PURPOSE:To prevent any scattering of an active material powder by treating the surface of a pasted cadmium electrode containing cadmium oxide as the main active material with an aqueous solution of a water-soluble macromolecular compound to form a thin layer of the compound on the surface. CONSTITUTION:After an active material powder principally composed of cadmium oxide is mixed with a dispersion medium such as aqueous PVA solution and a binder such as polyethylene to prepare a paste, the paste is applied to a core material. After that, an aqueous solution of a water-soluble macromolecular compound such as carboxymethylcellulose with a concentration of 0.5-1.5wt% is applied to the surface of the paste-coated material before drying the thus formed body, thereby making a cadmium electrode for an alkaline storage battery such as a nickel cadmium storage battery. Since the surface of the electrode is covered by a thin film of the water-soluble macromolecular compound, the electrode has increased mechanical strength and any scattering of the active material powder is prevented. Therefore, it is possible to improve the environment of manufacturing without influencing battery performance.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はニッケル・カドミウム蓄電池等のアルカリ蓄電
池の製造方法に関し、特に力下ミウム電極の表面に水溶
性高分子からなる薄層を形成させることを特徴とするア
ルカリ蓄電池の製造方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method for manufacturing alkaline storage batteries such as nickel-cadmium storage batteries, and is particularly characterized by forming a thin layer of water-soluble polymer on the surface of a nickel-cadmium electrode. The present invention relates to a method of manufacturing an alkaline storage battery.

従来の技術と発明が解決しようとする問題点アルカリ蓄
電池に使用されるカドミウム負極板には、一般にカルボ
ニルニッケル粉末を焼結させた多孔性基板に活物質を含
浸させた焼結式極板と、酸化カドミウム、ニッケル粉末
、増粘剤、樹脂。
Problems to be Solved by the Prior Art and the Invention Cadmium negative electrode plates used in alkaline storage batteries generally include a sintered electrode plate in which a porous substrate made of sintered carbonyl nickel powder is impregnated with an active material. Cadmium oxide, nickel powder, thickener, resin.

繊維等の混合物に分散媒を加え、適当な粘稠性を有する
ペースト状となし、これを電導性芯体上に塗着したペー
スト式極板がある。一般にペースト式極板の方が製造工
程数が少ないため、焼結式極板に比べ安価であるが°、
反面、極板の機械的強度が弱く、活物質粉末が飛散しや
すく、−極板製造時および電池組立時での作業環境が悪
いという問題があった。
There is a paste-type electrode plate in which a dispersion medium is added to a mixture of fibers, etc. to form a paste having an appropriate viscosity, and this is coated on a conductive core. In general, paste-type electrode plates require fewer manufacturing steps and are therefore cheaper than sintered-type electrode plates.
On the other hand, there were problems in that the mechanical strength of the electrode plate was weak, the active material powder was easily scattered, and - the working environment was poor during electrode plate manufacture and battery assembly.

問題点を解決するための手段 アルカリ蓄電池の製造に際して、酸化カドミウムを主活
物質とするペースト式カドミウム電極の表面を、水溶性
高分子の水溶液で処理して表面に水溶付高分子からなる
薄層を形成させることを特徴とするものである。
Means to Solve the Problem When manufacturing alkaline storage batteries, the surface of a paste-type cadmium electrode whose main active material is cadmium oxide is treated with an aqueous solution of a water-soluble polymer to form a thin layer of water-soluble polymer on the surface. It is characterized by forming.

極板表面を水溶性高分子の水溶液で処理して表面に水溶
性高分子のi1層を形成させる前のカドミウム電極は通
常の方法で製造される。例えば酸化カドミウムを主成分
としその他に金属カドミウムやニッケル粉末などを含有
する活物質粉末に、PVA水溶液などの分散媒とポリエ
チレン、繊維などの結合剤を混合し、次いで水を加えて
ペースト状とし、これを金fil製(例えばニッケルメ
ッキを施した多孔性鋼板)の集電芯体に塗着し、乾燥し
てカドミウム電極を製作した。
The cadmium electrode is manufactured by a conventional method before the surface of the electrode plate is treated with an aqueous solution of a water-soluble polymer to form an i1 layer of a water-soluble polymer on the surface. For example, an active material powder containing cadmium oxide as a main component and metal cadmium or nickel powder is mixed with a dispersion medium such as a PVA aqueous solution and a binder such as polyethylene or fiber, and then water is added to form a paste. This was applied to a current collector core made of gold film (for example, a porous steel plate plated with nickel) and dried to produce a cadmium electrode.

次に上記で1ηられたカドミウム電極は水溶性高分子の
水溶液で処理し、乾燥させて製作される。
Next, the cadmium electrode prepared above is manufactured by treating it with an aqueous solution of a water-soluble polymer and drying it.

水溶性高分子の水溶液でカドミウム電極の表面を処理す
る方法はハケで塗布したり、ローラによる塗布、霧状に
して噴霧するなどのカドミウム電極表面に均一に水溶性
高分子の水溶液を付与できる方法であればどんな方法で
もよい。
Methods for treating the surface of a cadmium electrode with an aqueous solution of a water-soluble polymer include coating with a brush, coating with a roller, or spraying in the form of a mist, which can uniformly apply an aqueous solution of a water-soluble polymer to the surface of the cadmium electrode. Any method is fine.

水溶性高分子としてはCMC,MCまたはPvAが用い
られが、これらはそれぞれ異なった特徴を有している。
CMC, MC, or PvA are used as water-soluble polymers, and each of these has different characteristics.

即ちCMCはMCやPVAとくらべて分子鎖が糸まり状
で溶解するため、同−m度でのi1層の強度が弱く比較
的添加量を多くしなければならないが、CMCがイオン
性であるため、電解液中で溶解しやすく、電解液や酸素
ガスの拡散を妨げることが少ないため高率/i5[?t
やガス吸収性能などの電池性能に悪影響をおよぼさない
In other words, compared to MC and PVA, CMC dissolves in the form of strings of molecular chains, so the strength of the i1 layer at the same -m degree is weak and a relatively large amount must be added, but CMC is ionic. Therefore, it is easily dissolved in the electrolyte and does not hinder the diffusion of the electrolyte and oxygen gas, so it has a high ratio /i5[? t
It does not adversely affect battery performance such as gas absorption performance.

これに対してMO′?1PVAはCMCと(らべて分子
鎖が伸びきった状態で溶解するため、同一濃度での薄層
の強度が強く比較的添加量を少なくできる。さらにMC
やP V A−は非イオン性であり、電解液中で安定で
あるが、添加量を少なくすることにより、電解液や酸素
ガスの拡散を妨げることが少なくなり、高率放電やガス
吸収性能などの電池性能に悪影響をおよぼさない。
MO' for this? 1PVA dissolves with the molecular chain fully extended compared to CMC, so the strength of the thin layer at the same concentration is strong and the amount added can be relatively small.
PVA- and PVA- are non-ionic and stable in the electrolyte, but by reducing the amount added, there is less interference with the diffusion of the electrolyte and oxygen gas, improving high rate discharge and gas absorption performance. Does not adversely affect battery performance.

このような水溶性高分子の水溶液の濃度は0.5〜1.
5wt%までのものが用いられ、この範囲未満の濃度の
ものでは、生成する水溶性高分子の薄層が弱くてはがれ
やすい傾向があり好ましくない。
The concentration of such an aqueous solution of water-soluble polymer is 0.5 to 1.
A concentration of up to 5 wt% is used, and concentrations below this range are not preferred because the resulting thin layer of water-soluble polymer tends to be weak and easily peel off.

一方ζ上記の範囲を越えると電極表面に生成する水溶性
高分子の層が厚くなり、ガス吸収性能や高率放電性能な
どの電池性能に悪影響を及ぼす。
On the other hand, if ζ exceeds the above range, the water-soluble polymer layer formed on the electrode surface becomes thick, which adversely affects battery performance such as gas absorption performance and high rate discharge performance.

電極表面に付与される水溶性高分子の適切な種類と濃度
は、電極の種類によって異なるが、上記のような理由で
、水溶性高分子のumが強固でしかも電池性能に悪影響
をおよぼさないものが適宜選択される。
Appropriate types and concentrations of water-soluble polymers applied to the electrode surface vary depending on the type of electrode, but for the reasons mentioned above, it is important that the water-soluble polymer um is strong and does not adversely affect battery performance. Those that are not available are selected as appropriate.

作用 本発明の方法によれば得られた電極は、表面が水溶性高
分子の薄層で覆われているために、極板の機械的強度が
強くなり、活物質粉末の飛散がほぼ、′完全に防止され
、極板製造時および電池組立時の作業環境が著しく改善
される。また水溶性高分子の種類と1度を適宜選択する
ことにより、高率放電やガス吸収性能などの電池性能に
悪影響をおよぼすことはない。
Function: Since the surface of the electrode obtained according to the method of the present invention is covered with a thin layer of water-soluble polymer, the mechanical strength of the electrode plate is strong, and the scattering of the active material powder is almost completely suppressed. This is completely prevented, and the working environment during electrode plate manufacturing and battery assembly is significantly improved. Furthermore, by appropriately selecting the type and degree of water-soluble polymer, battery performance such as high rate discharge and gas absorption performance will not be adversely affected.

実施例 (イ)カドミウム負極板の製作 酸化カドミウム粉末100重量部、金属カドミウム粉末
10重量部とニッケル粉末7重量部よりなる活物質粉末
に、クエン酸カリウム0.5重量部、MC011重量一
部、ナイロン単m維1!11部を加え充分混合し、次い
で水30重量部を加えてペースト状とした。このペース
トをニッケルメッキを施した多孔性鋼板の集電芯体に塗
着し乾燥してペースト式カドミウム電極(60G++n
 x300im x 0.7m+Ilt )を製作した
Example (a) Production of cadmium negative electrode plate Active material powder consisting of 100 parts by weight of cadmium oxide powder, 10 parts by weight of metal cadmium powder and 7 parts by weight of nickel powder, 0.5 part by weight of potassium citrate, part by weight of MC011, 1.11 parts of single meter nylon fibers were added and thoroughly mixed, and then 30 parts by weight of water was added to form a paste. This paste was applied to a current collector core made of nickel-plated porous steel plate and dried to form a paste-type cadmium electrode (60G++n
x300im x 0.7m+Ilt) was manufactured.

得られたペースト式カドミウム電極の表面にそれぞれ、
0. 0,5. 1,0. 1.5. 2.0wt%の
CMC水溶液をO−ラで均一に塗布し、乾燥させた後、
所定の寸法に切断してカドミウム負極板を製作した。
On the surface of the obtained paste-type cadmium electrode,
0. 0,5. 1,0. 1.5. After applying a 2.0 wt% CMC aqueous solution uniformly with an O-ra and drying it,
A cadmium negative electrode plate was manufactured by cutting it into predetermined dimensions.

(ロ)ニッケル・カドミウム蓄電池の製作前述の如く製
作したそれぞれのカドミウム負極    −板を、所定
寸法に切断したニッケル正極板と組合せ、セパレータを
介して渦巻状に巻き取り、ニッケルメッキを施した円筒
状かんに挿入し、比m1.25の水酸化カリウムを電解
液として注液して、上部に圧力計を取りつけて、容11
1800 mA hの密閉形円筒状ニッケル・カドミウ
ム蓄電池を製作した。
(b) Production of nickel-cadmium storage battery Each cadmium negative electrode plate produced as described above is combined with a nickel positive electrode plate cut to a predetermined size, and wound into a spiral shape through a separator to form a nickel-plated cylinder. Insert it into a can, pour potassium hydroxide with a ratio of 1.25 m as an electrolyte, attach a pressure gauge to the top, and make the volume 11.
A sealed cylindrical nickel-cadmium storage battery of 1800 mAh was fabricated.

(ハ)特性の比較 前述の如く製作したカドミウム負極板の切断時および電
池組立時の活物質粉末の飛散状態の結果を表に示す。
(c) Comparison of properties The results of the scattering state of active material powder during cutting of the cadmium negative electrode plate produced as described above and during battery assembly are shown in the table.

表 上表の如<CMC水溶液の濃度をo、swt%以上のも
のを選ぶことによって、極板製造時および電池組立時の
活物質粉末の飛散は完全に防止することができる。
As shown in the table above, by selecting the concentration of the CMC aqueous solution to be at least 0.swt%, it is possible to completely prevent the active material powder from scattering during electrode plate manufacture and battery assembly.

次に、前述の如く作製したそれぞれの蓄電池を、20℃
の雰囲気下で、0.1Cで16時間充電し、0.2Cで
0.8V/セルまで放電したのち、充電電流を0.1(
、、0,2C,0,50と変化させて、それぞれの電流
で160%充電した時の充電末期の電池内部圧力を読み
とり、ガス吸収性能を調べた結果を第1図に示す。同図
中特性AはCMC水溶液で処理していない従来のカドミ
ウム負極板を用いたものであり、特性B、C,D、Eは
順にCMC水溶液の濃度をo、swt%、  1.0w
t%、  1.5wt%、および2.0wt%にしたカ
ドミウム負極板を用いたものである。
Next, each storage battery produced as described above was heated at 20°C.
After charging at 0.1C for 16 hours and discharging to 0.8V/cell at 0.2C in an atmosphere of
, , 0.2C, 0.50C, the internal pressure of the battery was read at the end of charging when the battery was charged to 160% at each current, and the gas absorption performance was investigated. The results are shown in Figure 1. In the figure, characteristic A uses a conventional cadmium negative electrode plate that has not been treated with a CMC aqueous solution, and characteristics B, C, D, and E are obtained by changing the concentration of the CMC aqueous solution to o, swt%, and 1.0w, respectively.
t%, 1.5wt%, and 2.0wt% cadmium negative electrode plates were used.

この図から明らかなように、CMC水溶液の濃度が高い
程、特に2 wt%になるとガス吸収性能が悪くなる。
As is clear from this figure, the higher the concentration of the CMC aqueous solution, especially 2 wt%, the worse the gas absorption performance becomes.

また、CMC水溶液の′a度が小さいと、カドミウム負
極表面の薄層の強度が小さくなり、活物質粉末の飛散が
大きくなる。
Furthermore, if the a degree of the CMC aqueous solution is low, the strength of the thin layer on the surface of the cadmium negative electrode will be low, and the scattering of the active material powder will be large.

このように、CMC水溶液の濃度が大きいと、カドミウ
ム負極表面の薄層の強度は大きいが、ガスや電解液の拡
散が悪くなり、ガス吸収性能が低下することになるので
、CMC水溶液の1I11度は0、 SV t%〜1.
5wt%が好ましい。
In this way, when the concentration of the CMC aqueous solution is high, the strength of the thin layer on the surface of the cadmium negative electrode is high, but the diffusion of gas and electrolyte becomes poor, and the gas absorption performance decreases. is 0, SV t%~1.
5 wt% is preferred.

発明の効果 以上の如く本発明はカドミウム電極の表面が水溶性高分
子の薄層で覆われるために、極板の機械的強度が強くな
り、活物質粉末の飛散が完全に防止され、極板製造時お
よび電池組立時の作業環境が著しく改善される。また、
水溶性高分子の種類と濃度を適宜選択することによって
、^率放電やガス吸収性能などの電池性能に悪影響をお
よぼすことはない。
Effects of the Invention As described above, in the present invention, since the surface of the cadmium electrode is covered with a thin layer of water-soluble polymer, the mechanical strength of the electrode plate is increased, the scattering of the active material powder is completely prevented, and the electrode plate is The working environment during manufacturing and battery assembly is significantly improved. Also,
By appropriately selecting the type and concentration of the water-soluble polymer, battery performance such as rate discharge and gas absorption performance will not be adversely affected.

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

第1図はCMC水溶液の11度を異にした場合の蓄電池
内の内部圧力特性図である。 Δ・・・従来品、8〜E・・・本発明品′)r  1 
 回 光 電 々 環 ((:A)
FIG. 1 is a diagram showing the internal pressure characteristics in the storage battery when the CMC aqueous solution is varied by 11 degrees. Δ...Conventional product, 8~E...Invention product') r 1
Circular electric ring ((:A)

Claims (1)

【特許請求の範囲】 1、酸化カドミウムを主活物質とするペースト式カドミ
ウム電極の表面を、水溶性高分子の水溶液で処理して、
表面に水溶性高分子からなる薄層を形成させることを特
徴とするアルカリ蓄電池の製造方法。 2、水溶性高分子がカルボキシメチルセルロース(以下
CMCという)、メチルセルロース(以下MCという)
またはポリビニルアルコール(以下PVAという)であ
る特許請求の範囲第1項記載のアルカリ蓄電池の製造方
法。 3、水溶性高分子の水溶液の濃度が0.5wt%〜1.
5wt%である特許請求の範囲1項または第2項記載の
アルカリ蓄電池の製造方法。
[Claims] 1. The surface of a paste-type cadmium electrode containing cadmium oxide as the main active material is treated with an aqueous solution of a water-soluble polymer,
A method for producing an alkaline storage battery, characterized by forming a thin layer made of a water-soluble polymer on the surface. 2. Water-soluble polymers include carboxymethylcellulose (hereinafter referred to as CMC) and methylcellulose (hereinafter referred to as MC)
or polyvinyl alcohol (hereinafter referred to as PVA), the method for producing an alkaline storage battery according to claim 1. 3. The concentration of the water-soluble polymer aqueous solution is 0.5 wt% to 1.
The method for manufacturing an alkaline storage battery according to claim 1 or 2, wherein the content is 5 wt%.
JP60045556A 1985-03-06 1985-03-06 Manufacture of alkaline storage battery Pending JPS61203559A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60045556A JPS61203559A (en) 1985-03-06 1985-03-06 Manufacture of alkaline storage battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60045556A JPS61203559A (en) 1985-03-06 1985-03-06 Manufacture of alkaline storage battery

Publications (1)

Publication Number Publication Date
JPS61203559A true JPS61203559A (en) 1986-09-09

Family

ID=12722631

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60045556A Pending JPS61203559A (en) 1985-03-06 1985-03-06 Manufacture of alkaline storage battery

Country Status (1)

Country Link
JP (1) JPS61203559A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1037215C (en) * 1993-07-28 1998-01-28 机械电子工业部第十八研究所 Method for making Ni substrate sintered by high-porosity slurry-scraping method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5028644A (en) * 1973-07-17 1975-03-24
JPS5386442A (en) * 1977-01-10 1978-07-29 Matsushita Electric Ind Co Ltd Negative electrode for alkaline storage battery
JPS60202666A (en) * 1984-03-26 1985-10-14 Sanyo Electric Co Ltd Paste type cadmium anode plate for alkaline storage battery

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5028644A (en) * 1973-07-17 1975-03-24
JPS5386442A (en) * 1977-01-10 1978-07-29 Matsushita Electric Ind Co Ltd Negative electrode for alkaline storage battery
JPS60202666A (en) * 1984-03-26 1985-10-14 Sanyo Electric Co Ltd Paste type cadmium anode plate for alkaline storage battery

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1037215C (en) * 1993-07-28 1998-01-28 机械电子工业部第十八研究所 Method for making Ni substrate sintered by high-porosity slurry-scraping method

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