JPS62103987A - Method of injecting electrolyte into sealed lead battery - Google Patents

Method of injecting electrolyte into sealed lead battery

Info

Publication number
JPS62103987A
JPS62103987A JP60243701A JP24370185A JPS62103987A JP S62103987 A JPS62103987 A JP S62103987A JP 60243701 A JP60243701 A JP 60243701A JP 24370185 A JP24370185 A JP 24370185A JP S62103987 A JPS62103987 A JP S62103987A
Authority
JP
Japan
Prior art keywords
electrolyte
fibers
solution
glass
electrode plates
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
JP60243701A
Other languages
Japanese (ja)
Inventor
Toshiyuki Matsumura
敏之 松村
Tsuneo Fujishiro
藤城 恒夫
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.)
Resonac Corp
Original Assignee
Shin Kobe Electric Machinery 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 Shin Kobe Electric Machinery Co Ltd filed Critical Shin Kobe Electric Machinery Co Ltd
Priority to JP60243701A priority Critical patent/JPS62103987A/en
Publication of JPS62103987A publication Critical patent/JPS62103987A/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
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/06Lead-acid accumulators
    • H01M10/12Construction or manufacture
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/60Arrangements or processes for filling or topping-up with liquids; Arrangements or processes for draining liquids from casings
    • H01M50/609Arrangements or processes for filling with liquid, e.g. electrolytes
    • 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

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Secondary Cells (AREA)

Abstract

PURPOSE:To lengthen life, by pouring in more than a prescribed amount of an electrolytic solution to impregnate the solution into a cathode and an anode plates and fibers of glass or the like, and draining the excess of the solution, to put the electrode plates in sure contact with the fibers to suppress the increase in internal resistance. CONSTITUTION:An electrode plate group comprising a cathode plate 1, 2 anode plates 2 and fibers 3 of glass or the like filled between the electrode plates to hold an electrolytic solution and separate the electrode plates from each other is provided. A solution drain hole 6 is provided in the bottom of a battery jar 5. The fibers 3 of glass or the like are filled between the electrode plates so that the fibers are put in sure contact with the entire sides of the electrode plates. While the solution drain hole 6 is closed by a plug, more than a prescribed amount of the electrolytic solution is poured into the battery jar 5 so that the solution is surely impregnated into the electrode plates and the fibers 3. After that, the plug is removed to drain the excess of the electrolytic solution.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はシール鉛電池の電解液注入方法に関Tるもので
ある。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a method for injecting electrolyte into sealed lead-acid batteries.

従来の技術 一般にシール鉛電池は、陽極で発生した酸素ガスを陰極
板で吸収する陰極ガス吸収方式を採用している。そのた
め、電解液は陽極板、陰極板およびリテーナと称される
ガラス繊維等の不織布あるいは織布に含浸されるだけで
、遊離電解液は存在しない構造となっている。
BACKGROUND OF THE INVENTION Generally, sealed lead batteries employ a cathode gas absorption method in which oxygen gas generated at an anode is absorbed by a cathode plate. Therefore, the structure is such that the electrolyte is only impregnated into the anode plate, the cathode plate, and a nonwoven or woven fabric such as glass fiber called a retainer, and no free electrolyte exists.

従来行なわれている一般的な電解液注入方法としては、
あう小じめ陽島板、陰極板、および発明が解決しようと
Tるl¥J1曜点 上起点上記ろに、シール鉛電池は、陰極ガス吸収方式ン
採用しているため、液量を制限し遊離電解液を持たない
構造としている。そのため、電解液を含浸保持する、陽
極板および陰極板の活物質やリテーナの重量及び寸法等
を厳重に管理し、一定の液量な確保Tるようにしている
The conventional general electrolyte injection method is as follows:
The sealed lead battery uses a cathode gas absorption method, which limits the amount of liquid. The structure has no free electrolyte. Therefore, the weight and dimensions of the active materials of the anode and cathode plates and the retainer that impregnate and retain the electrolytic solution are strictly controlled to ensure a constant amount of the electrolyte.

し刀)シ、現在のペースト充填法ではバラツキなく充填
量をそろえることは困難であり、セル毎に含み得る電解
液量も微妙に異なってくるため、一定量の電解液を注入
した場会は、必ずしも最適液量になるとは限らない。
However, with the current paste filling method, it is difficult to uniformly fill the filling amount, and the amount of electrolyte that can be contained in each cell varies slightly, so when a fixed amount of electrolyte is injected, , the optimum liquid volume may not necessarily be achieved.

シール鉛電池番ズ、陽極板力)ら発生した酸素は陰極板
で吸収さt水lこ戻るため減液はないが、光放電サイク
ルの光電末期や浮動充電時には陰極板でのガス吸収は1
00亮でなく偶力)の酸素ガスが放出する。この時水蒸
気の放出も同時Iζ行なわれ、使用中に減液が進行する
。減液量が多くなると、極板とリテーナの接触抵抗が極
度に増大し電池の内部抵抗が増大し、容量が低下する。
Oxygen generated from the sealed lead battery (sealed lead battery, anode plate force) is absorbed by the cathode plate and water returns, so there is no liquid reduction, but at the end of the photodischarge cycle or during floating charging, the gas absorption at the cathode plate is 1.
Oxygen gas is released. At this time, water vapor is also released at the same time, and liquid reduction progresses during use. When the amount of liquid reduction increases, the contact resistance between the electrode plate and the retainer increases extremely, the internal resistance of the battery increases, and the capacity decreases.

この現象は初期に適切な電解液量が注入されていないと
、より加速さn%極端な堝含には初期の容量バラツキを
招く七いう欠点を有していた。
This phenomenon has the disadvantage that if an appropriate amount of electrolyte is not initially injected, it will be accelerated, leading to initial capacity variations at n% extreme levels.

第2図は、従来のシール鉛電池の極板群構成の概略を示
すものであるが、陽極板1にU字状にリテーナである隔
離体4を巻き、その外側部に陰極板2?!/配置した構
造である。この極板群中の電解液の分布を容量が1.8
Ah(10yqw )の電池を例として第3図に示す0
この極板群の含み得る最大電解液量は17.5−である
。減液が起こると第3図から明ら力)なように陰極板1
および陰極板2の含液量は変化がな77)ったが−隔離
体4中の電解液が減少して行く。これは陽極板1および
陰極板2の活物質の孔径と隔離体・lの見かけの空間径
の大きさの違いによるものであり、空間径の大きい隔離
体4中の電解液が減少したためである。
FIG. 2 schematically shows the configuration of the electrode plate group of a conventional sealed lead-acid battery.A separator 4, which is a retainer, is wrapped around the anode plate 1 in a U-shape, and a cathode plate 2 is placed on the outside of the separator 4. ! /It is a structure arranged. The distribution of electrolyte in this electrode plate group has a capacity of 1.8
Taking the Ah (10yqw) battery as an example, the 0
The maximum amount of electrolyte that this electrode plate group can contain is 17.5-. When liquid reduction occurs, it is clear from Figure 3 that the cathode plate 1
Although the liquid content of the cathode plate 2 remains unchanged 77), the electrolyte in the separator 4 decreases. This is due to the difference in the pore size of the active materials of the anode plate 1 and the cathode plate 2 and the apparent space diameter of the separator l, and is due to the decrease in the electrolyte in the separator 4, which has a large space diameter. .

現在のペースト充填法では極板厚みおよび平滑Fのバラ
ツキ、パックリング等により極板と隔離体4の接触が部
分的lこ不十分lこなることがある。また、活物質季の
バラツキにより電解液の含浸量も異なってくるため、電
解液の減少が生じると、極板と隔離体4の接触抵抗が極
度に増大し、電池の内部抵抗が増加して早期に容量低下
を招いたり、極端な場会には初期の容量バラツキを招く
という欠点を有していた0本発明は上記欠点を除去する
こと全目的と下るものである。
In the current paste filling method, the contact between the electrode plate and the separator 4 may be partially insufficient due to variations in the electrode plate thickness and smoothness F, pack ring, etc. Furthermore, since the amount of electrolyte impregnated varies depending on the variation in the active material season, when the amount of electrolyte decreases, the contact resistance between the electrode plate and the separator 4 increases extremely, and the internal resistance of the battery increases. The entire purpose of the present invention is to eliminate the above-mentioned drawbacks, which have the disadvantage of causing an early capacity drop or, in extreme cases, causing an initial variation in capacity.

問題点を解決するための手段 上記の目的を達gTlために、本発明は、枠板間にガラ
ス等の禮##を介在させるとともに、所定液量を越える
電解液を注入し確実に単極板、陰極板Sよびガラス等の
繊維な介在させた部分へ電解液?含浸させた後、排出孔
より余剰”s4E′4液?排出することにより適正電解
液量を確保するものである。
Means for Solving the Problems In order to achieve the above object, the present invention interposes a material such as glass between the frame plates, and injects an electrolyte exceeding a predetermined amount to ensure monopolarity. Electrolyte to intervening parts such as plates, cathode plates, glass, etc.? After impregnation, the excess "s4E'4" liquid is discharged from the discharge hole to ensure an appropriate amount of electrolyte.

作用 これにより、極板4み2よび平滑度のバラツキ、あるい
はバックリング等が生じた場曾においても、b板とガラ
ス等の線維ンN実に接触させて内部抵抗の増加全抑制し
て寿命?向上することができる。
As a result, even if variations in the smoothness of the electrode plates or buckling occur, the increase in internal resistance can be completely suppressed by bringing the B plate into contact with the fibers such as glass, thereby reducing the lifespan. can be improved.

実施例 本発明の一笑流側?第1図番二より説明する。Example The laughing side of this invention? This will be explained starting from Figure 1, number 2.

陽極板1が1枚、陰極板2が2枚、該極板間に電解液の
保持および該極板の隔離の役目をするガラス等の線維3
を充填してなる極板r#を有し、[槽5の底部に排液孔
6を配した構造のシール鉛電池ン示す。
One anode plate 1, two cathode plates 2, and fibers 3 such as glass that serve to hold the electrolyte between the plates and isolate the plates.
A sealed lead-acid battery having a structure in which a drain hole 6 is arranged at the bottom of a tank 5 is shown.

このように、極板間にガラス等のM!!維3を充填して
介在させることによ11.極板の全面とガラス等の繊維
3を確実に接触させることができる。電解液の注入は、
最初セル底部の排液孔6の栓?閉じておき、所定液量よ
t)多い欲の電解液?注入して確実に1!極およびガラ
ス等の繊維3に含?2Tる。方法としては長時間放置下
るとか、減圧状態にして脱気Tる等の方法がある。
In this way, M! of glass etc. is placed between the electrode plates. ! 11. By filling and intervening the fibers 3. The entire surface of the electrode plate can be brought into reliable contact with the fibers 3 such as glass. The injection of electrolyte is
First, is the drain hole 6 plug at the bottom of the cell? Keep it closed and use the specified amount of electrolyte. Inject it for sure! Contained in fiber 3 such as poles and glass? 2Tru. Methods include leaving it for a long time or degassing it under reduced pressure.

含没後栓YCズずして余剰の電解液を排出7る。After impregnation, remove the plug YC to drain excess electrolyte 7.

本発明による構造のシール鉛電氾と従来構造のシール鉛
電?l!1. (何れも6M1.Fl型)k常法ζこ、
J−1〜作し、40℃、6.8v連続定電圧過充電試験
を行っ7zo結果ytm4図に示すが、従来のシール鉛
電池がV:J部抵抗の上昇により1.0年弱で容量が低
下したのに対し、本発明によるシール鉛11i fil
Hは1.5年程度とflt′Lでいた。
Seal lead-acid flood with the structure according to the present invention and seal lead-acid flood with the conventional structure? l! 1. (Both are 6M1.Fl type)k ordinary method ζko,
A continuous constant voltage overcharge test of 6.8V was carried out at 40°C, and the results are shown in the figure YTM4. The conventional sealed lead batteries lost capacity in less than 1.0 years due to an increase in resistance at the V:J section. The seal lead 11i fil according to the present invention decreased.
H was flt'L for about 1.5 years.

発明の効果 上述のように、本発明の電解液注入方法を採用すること
により、極板およびガラス等の繊維にvr火fC宙解液
を含浸させ得、b板とガラス等の#維の接触抵抗を低く
抑えて優れた電池40命が得らlする等工業的価値極め
て大なるものであるO
Effects of the Invention As described above, by employing the electrolyte injection method of the present invention, it is possible to impregnate the electrode plate and fibers such as glass with the VR fire fC cosmolysis solution, and to prevent contact between the b plate and # fibers such as glass. It has great industrial value, such as keeping the resistance low and providing an excellent battery life of 40 hours.

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

第1囚は本発明の一実施例におけるシール鉛電池な示す
断面概略図、第2囚は従来のシール鉛電池を示す断面概
略図、第3図は極板群中の電解液の分布図、第4図は本
発明により得られるシール鉛電池と従来のシール鉛電池
における定電圧寿命試験結果を示す曲線図である。
The first cell is a schematic cross-sectional view showing a sealed lead battery according to an embodiment of the present invention, the second cell is a schematic cross-sectional view showing a conventional sealed lead battery, and FIG. 3 is a distribution diagram of the electrolyte in the electrode plate group. FIG. 4 is a curve diagram showing the results of a constant voltage life test on a sealed lead battery obtained according to the present invention and a conventional sealed lead battery.

Claims (1)

【特許請求の範囲】[Claims] 極板間に成形されていないガラス等の繊維を介在させる
とともにセル底部に排液孔を配したシール鉛電池におい
て、所定液量を越える電解液を注入し陽極板、陰極板お
よびガラス等の繊維を介在させた部分へ電解液を含浸さ
せた後、排液孔より余剰電解液を排出することにより極
板群中に適正液量を確保することを特徴とするシール鉛
電池の電解液注入方法。
In a sealed lead-acid battery that has an unmolded glass or other fiber interposed between the electrode plates and a drainage hole at the bottom of the cell, an electrolyte exceeding a predetermined amount is injected to remove the anode plate, cathode plate, and glass or other fiber. A method for injecting an electrolyte into a sealed lead-acid battery, characterized by impregnating a portion with an electrolyte in between, and then draining excess electrolyte from a drainage hole to ensure an appropriate amount of electrolyte in the electrode plate group. .
JP60243701A 1985-10-30 1985-10-30 Method of injecting electrolyte into sealed lead battery Pending JPS62103987A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60243701A JPS62103987A (en) 1985-10-30 1985-10-30 Method of injecting electrolyte into sealed lead battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60243701A JPS62103987A (en) 1985-10-30 1985-10-30 Method of injecting electrolyte into sealed lead battery

Publications (1)

Publication Number Publication Date
JPS62103987A true JPS62103987A (en) 1987-05-14

Family

ID=17107698

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60243701A Pending JPS62103987A (en) 1985-10-30 1985-10-30 Method of injecting electrolyte into sealed lead battery

Country Status (1)

Country Link
JP (1) JPS62103987A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5323934A (en) * 1976-08-17 1978-03-06 Bayer Ag Novel asymmetric o*oodialkylloovinyl thionophosphoric ester* preparation thereof and arthropocidal composition containing same as active composition
JPS54114727A (en) * 1978-02-28 1979-09-07 Shin Kobe Electric Machinery Method of producing lead storage battery
JPS58216356A (en) * 1982-06-10 1983-12-16 Matsushita Electric Ind Co Ltd Instant lead storage battery jar and production method of instant lead storage battery

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5323934A (en) * 1976-08-17 1978-03-06 Bayer Ag Novel asymmetric o*oodialkylloovinyl thionophosphoric ester* preparation thereof and arthropocidal composition containing same as active composition
JPS54114727A (en) * 1978-02-28 1979-09-07 Shin Kobe Electric Machinery Method of producing lead storage battery
JPS58216356A (en) * 1982-06-10 1983-12-16 Matsushita Electric Ind Co Ltd Instant lead storage battery jar and production method of instant lead storage battery

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