JPS62105370A - Manufacture of cathode plate for alkaline storage battery - Google Patents
Manufacture of cathode plate for alkaline storage batteryInfo
- Publication number
- JPS62105370A JPS62105370A JP60244683A JP24468385A JPS62105370A JP S62105370 A JPS62105370 A JP S62105370A JP 60244683 A JP60244683 A JP 60244683A JP 24468385 A JP24468385 A JP 24468385A JP S62105370 A JPS62105370 A JP S62105370A
- Authority
- JP
- Japan
- Prior art keywords
- active material
- nickle
- aqueous solution
- sintered
- salt
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/24—Electrodes for alkaline accumulators
- H01M4/26—Processes of manufacture
- H01M4/28—Precipitating active material on the carrier
-
- 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)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明はアルカリ蓄電池用陽極板の製造法の改良に関す
るものである。DETAILED DESCRIPTION OF THE INVENTION FIELD OF INDUSTRIAL APPLICATION The present invention relates to an improvement in the manufacturing method of anode plates for alkaline storage batteries.
従来の技術
従来、アルカリ蓄電池の陽極板は、ニッケル焼結基体を
所定活物質塩の水溶液に浸漬し、次いでアルカリ水溶液
中で基体の細孔内の塩ビ水酸化物に置換し沈着せしめる
方法が一般lこ行なわれている。しっ)シ、高容量化と
いう最近の市場ニーズから陽権板の容重向上が望まれ、
活物質充填量乞増加させること及び活物質の利用率を向
上させることが不可欠となった。そこで高容量の陽梅板
乞製造するにめlこニッケル焼結基体の多孔度?増加せ
しめ、活物質充填量を高める方法や水酸化コバルト乞含
む水酸化ニッケルを主取分とする活物質の表面に水酸化
コバルト乞沈着せしめ利用率乞向上せしめる方法が提案
されている。Conventional technology Conventionally, the anode plate of an alkaline storage battery is generally produced by dipping a nickel sintered substrate in an aqueous solution of a specified active material salt, and then substituting and depositing PVC hydroxide in the pores of the substrate in the alkaline aqueous solution. This is being done. Sh) Shi, due to the recent market needs for higher capacity, it is desired to improve the capacity and weight of Yogon plates.
It has become essential to increase the active material loading and improve the active material utilization rate. Therefore, what is the porosity of the nickel sintered substrate used to produce high capacity plates? A method of increasing the active material filling amount and a method of increasing the utilization rate by depositing cobalt hydroxide on the surface of an active material mainly composed of nickel hydroxide containing cobalt hydroxide have been proposed.
発明が解決しようとする問題点
上記整造方法の中で、焼結基体の多孔度乞増加させ活物
質充填量を高める方法は、焼結基体の機械的強度が低下
するため光放電乞くり返した際に生じる活物質の膨化に
より焼結基体が多孔性金属芯材力)ら剥離する欠点乞有
している。Problems to be Solved by the Invention Among the above preparation methods, the method of increasing the porosity of the sintered substrate to increase the amount of active material filled in the sintered substrate reduces the mechanical strength of the sintered substrate, resulting in repeated photodischarges. This method has the disadvantage that the sintered substrate peels off from the porous metal core due to the swelling of the active material that occurs.
また水酸化コバルト7含む水酸化ニッケル乞生成分とす
る活物質の表面Eこ水酸化コバルトを沈着せしめ活物質
の利用率を向よせしめる方法では、活物質中の水酸化コ
バルトの含有量が多くなり、前記活物質の膨化を促進す
る等の問題がある。In addition, in the method of depositing cobalt hydroxide on the surface of the active material as a nickel hydroxide component containing cobalt hydroxide 7 to improve the utilization rate of the active material, the content of cobalt hydroxide in the active material is high. Therefore, there are problems such as promoting the expansion of the active material.
問題点を解決する之めの手段
本発明は上記の如き欠点乞除去するもので、ニッケル焼
結基体を低温度次いで高温度の所定活物質塩水溶液lこ
浸漬せしめるものである0作用
活物質塩の水溶液f1強酸性を有しているので、低温1
iHこ保持して酸化力を弱め浸漬時の焼結ニッケルの腐
食を和らげることによ1へ浸漬時間を長くせしめ焼結基
体内の細孔内への塩の浸透を十分lこ行なわせることが
できるので、活物質充填量の向上がはかれる。次に高温
度で酸化力の強い塩水溶液をこ短時間浸漬することによ
り、焼結ニッケルをわず力)に溶解せしめニッケル粒子
の表面を活物質化させることにより集電体であるニッケ
ル粒子と活物質の電気伝導性を高め利用率を向上せしめ
ることができる。Means for Solving the Problems The present invention eliminates the above drawbacks by immersing a nickel sintered substrate in a predetermined active material salt aqueous solution at low and then high temperatures. Since the aqueous solution f1 has strong acidity, the low temperature 1
By maintaining iH to weaken the oxidizing power and alleviate corrosion of the sintered nickel during immersion, it is possible to lengthen the immersion time and ensure sufficient penetration of the salt into the pores in the sintered substrate. Therefore, the amount of active material filled can be improved. Next, by immersing the sintered nickel in an aqueous salt solution with strong oxidizing power at high temperature for a short period of time, the sintered nickel is dissolved in water, and the surface of the nickel particles becomes an active material. It is possible to increase the electrical conductivity of the active material and improve the utilization rate.
実施例 本発明の一実施例を説明する。Example An embodiment of the present invention will be described.
ニッケル焼結基板(L50XW50XtO,50)を1
〜5wt%の硝酸コバルトY含有Tる液温50℃、比重
1.70の硝酸ニッケル水溶液lこ30分間浸漬し、次
fこ液温85℃、比重1.70の前記硝酸ニッケル水溶
液に5分間浸漬せしめt後、アルカリ水溶液中で活物質
充填量させ、アルカリを水洗するという操作を所定活物
’ttを得るまでくり返し行なった。次に、この極板を
ニッケル板7対極として31.2wt%の水酸化カリウ
ム水溶液中で水酸化ニッケルの理論容91こ対し0、2
0mA電流で10時間光光電性なった後、0.20m1
電流で放電を行ない活物質の利用率を求めた0
第1図は含浸操作:¥4回くり返し行なった際の活物質
充填量の比較乞示したものである。第2図は同−活物質
充填量における活物質利用率の比較を示したものである
。1 nickel sintered substrate (L50XW50XtO, 50)
~5 wt% of cobalt nitrate Y was immersed in a nickel nitrate aqueous solution with a liquid temperature of 50°C and a specific gravity of 1.70 for 30 minutes, and then immersed in the nickel nitrate aqueous solution with a liquid temperature of 85°C and a specific gravity of 1.70 for 5 minutes. After immersion, the operation of filling the active material in an alkaline aqueous solution and washing the alkali with water was repeated until a predetermined active material 'tt was obtained. Next, this electrode plate was used as a counter electrode with a nickel plate 7, and 0,2
After being photophotosensitive for 10 hours at 0 mA current, 0.20 m1
Figure 1 shows a comparison of the amount of active material filled when the impregnation operation was repeated four times. FIG. 2 shows a comparison of the active material utilization rate for the same amount of active material.
発明の効果
土述のようlこ、本発明は活物質充填量全増加せしめか
つ活物質利用率を向上ならしめることができる等工業的
価値きわめて大なるものである0Effects of the Invention As stated above, the present invention has extremely great industrial value, such as being able to increase the total amount of active material loaded and improve the active material utilization rate.
第1図は本発明の一実施例と従来法における活物質充填
量の比較図、第2図はそれぞれによって得られる場極板
lこBける活物質利用率の比較図1である。FIG. 1 is a comparison diagram of the amount of active material filled in an embodiment of the present invention and the conventional method, and FIG. 2 is a comparison diagram of the active material utilization rate in the field electrode plate obtained by each method.
Claims (1)
用陽極板の含浸工程において、焼結基体を低温度の所定
活物質塩の水溶液に浸漬せしめた後、さらに高温度の前
記水溶液中に浸漬し、次いでアルカリ水溶液中で焼結基
体内の塩類を水酸化物に置換せしめることを特徴とする
アルカリ蓄電池用陽極板の製造法。In the impregnation process of an anode plate for an alkaline storage battery in which an active material is filled into a nickel sintered substrate, the sintered substrate is immersed in an aqueous solution of a predetermined active material salt at a low temperature, and then further immersed in the aqueous solution at a high temperature. 1. A method for producing an anode plate for an alkaline storage battery, the method comprising: then replacing salts in the sintered substrate with hydroxides in an alkaline aqueous solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60244683A JPS62105370A (en) | 1985-10-31 | 1985-10-31 | Manufacture of cathode plate for alkaline storage battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60244683A JPS62105370A (en) | 1985-10-31 | 1985-10-31 | Manufacture of cathode plate for alkaline storage battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62105370A true JPS62105370A (en) | 1987-05-15 |
Family
ID=17122390
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60244683A Pending JPS62105370A (en) | 1985-10-31 | 1985-10-31 | Manufacture of cathode plate for alkaline storage battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62105370A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59165370A (en) * | 1983-03-09 | 1984-09-18 | Sanyo Electric Co Ltd | Manufacture of cathode plate for alkaline storage battery |
JPS6074262A (en) * | 1983-09-30 | 1985-04-26 | Furukawa Battery Co Ltd:The | Manufacture of nickel electrode |
-
1985
- 1985-10-31 JP JP60244683A patent/JPS62105370A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59165370A (en) * | 1983-03-09 | 1984-09-18 | Sanyo Electric Co Ltd | Manufacture of cathode plate for alkaline storage battery |
JPS6074262A (en) * | 1983-09-30 | 1985-04-26 | Furukawa Battery Co Ltd:The | Manufacture of nickel electrode |
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