JPS5946771A - Enclosed lead battery - Google Patents

Enclosed lead battery

Info

Publication number
JPS5946771A
JPS5946771A JP57157633A JP15763382A JPS5946771A JP S5946771 A JPS5946771 A JP S5946771A JP 57157633 A JP57157633 A JP 57157633A JP 15763382 A JP15763382 A JP 15763382A JP S5946771 A JPS5946771 A JP S5946771A
Authority
JP
Japan
Prior art keywords
battery
electrode plate
acid
plate group
electrolyte
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
JP57157633A
Other languages
Japanese (ja)
Inventor
Sadao Furuya
定男 古屋
Yoshihiro Kobayashi
小林 嘉博
Kenji Kobayashi
健二 小林
Hiroshi Yasuda
博 安田
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 JP57157633A priority Critical patent/JPS5946771A/en
Publication of JPS5946771A publication Critical patent/JPS5946771A/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
    • H01M10/34Gastight accumulators
    • H01M10/342Gastight lead accumulators
    • 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

Landscapes

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

Abstract

PURPOSE:To improve charge/discharge performance after overcharge and recovery capacity while to prevent overflow when forming the battery jar, by arranging acid-resistant porous material having liquid holding performance on the plate group. CONSTITUTION:Acid-resistant porous material 5 having liquid holding performance is arranged on a plate group 4 constructed with a positive pole plate 1, negative pole plate 2 and a separator 3 mainly composed of glass fiber. Said plate group 4 is inserted into a battery jar 8 then electrolyte or diluted sulfuric acid is injected throgh a liquid injection/discharge port 9 in the jar cover then an explosion-proof valve 10 made of rubber is fixed at the discharge port 9 to produce a small size enclosed lead battery. Consequently charge/discharge performance after over-discharge and recovery capacity are improved to prevent overflow when forming the battery jar.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、極板及びガラス繊維を主成分とするセパレー
タに電解液を含浸保持さ副−充電時に正極板より光生す
る酸素ガスを負極板にて吸収除去する密閉形鉛蓄電池に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is characterized in that an electrode plate and a separator mainly composed of glass fibers are impregnated with an electrolytic solution, and oxygen gas generated from the positive electrode plate during sub-charging is transferred to the negative electrode plate. This relates to a sealed lead-acid battery that absorbs and removes water.

従来例の構成とその問題点 密閉形鉛蓄電池を小形化し、エネルギー密度を向上させ
る上で最も重要な課題は、所望とする電池容量に必′万
な電池構成部品をせまい電池容器内空間にどの様に組み
込むかである。通常、第1図に示すように電池構成部分
である正極板1.負極板2及びガラス繊維製セパレータ
3ば、交互に積み重ねられ極板群4を構成して電池容器
内に組み込まノコ1.電解液は極板及びセ・ぐレータに
含浸保持されている。しかし電池構成部品中、極板及び
セ・くレータは一定形状を保ち1号るが、セ・くレータ
に含浸させた電解液は不定形であるため、様々な位16
において電池容器内空間に必要な電解液を惺持さぜる努
力がなさiしている、 例えば、実開昭63−113326号公報に示されるよ
うに棒板群の下部あるいは側部に配置し。
Conventional configurations and their problems The most important issue in downsizing sealed lead-acid batteries and improving their energy density is how to fit the battery components necessary for the desired battery capacity into a small space inside the battery container. It depends on how you incorporate it. Usually, as shown in FIG. 1, a positive electrode plate 1. The negative electrode plates 2 and glass fiber separators 3 are alternately stacked to form an electrode plate group 4, which is assembled into the battery container. The electrolyte is impregnated into the electrode plates and the separator. However, among the battery components, the electrode plate and the separator maintain a constant shape, but the electrolytic solution impregnated in the separator has an amorphous shape, so it varies in various positions.
For example, as shown in Japanese Utility Model Application Publication No. 63-113326, no effort has been made to maintain the necessary electrolyte in the space inside the battery container. .

だ多孔体に電解液を吸収させて、必要な電解液量を確保
することが考えられた、しかしこの方策は電池容量は満
足するが、過放電放置後の充電受入性と、その後の回復
容量の点で悪いことがわかった。また、電解液量を必要
容量以上に多く確保することは、小形化の目的にそぐわ
ない、そのため小形の密閉形鉛蓄電池の最大の欠点の一
つは、過放電放置後の充電受入性と−その後の回復容3
Bが悪いことにある、 また、未化成板から成る極板群を組み込んだ密閉形鉛蓄
電池に電解液を極板群の高さ以上に注入して化成を行う
、いわゆる電槽化成時に、小形化した電池は電解液量と
液栓部との距離が短かいだめ、化成に伴って発生する気
泡が液栓部の丁で割りて飛沫が液栓部に付着して排気孔
をふさぎ、電池内に発生したガスと共に外部に温液する
という現象が見らり、た。このような温液によるリーク
It was considered that the required amount of electrolyte could be obtained by absorbing the electrolyte into a porous material. However, although this method satisfied the battery capacity, it had problems with charge acceptance after over-discharging and subsequent recovery capacity. It turned out to be bad in that respect. In addition, securing a larger amount of electrolyte than the required capacity does not suit the purpose of miniaturization, so one of the biggest drawbacks of small sealed lead-acid batteries is the charge acceptance after over-discharging. recovery capacity 3
B is bad. In addition, during so-called battery cell formation, in which electrolyte is injected into a sealed lead-acid battery that incorporates an electrode group consisting of unformed plates to a level higher than the height of the electrode group, so-called battery cell formation, small In a battery that has become oxidized, the amount of electrolyte and the distance between the electrolyte and the liquid stopper are too short, and the air bubbles that are generated during formation are broken by the blades of the liquid stopper, resulting in droplets that adhere to the stopper and block the exhaust hole, causing the battery to leak. A phenomenon was observed in which hot liquid leaked outside along with the gas generated inside. Leak caused by hot liquid like this.

端子腐食等により、電槽化成を行なうことがむずかしい
だめ、小形の密閉形鉛蓄電池では、化成済み極板も用い
るのが一般的であ−だ。
Since it is difficult to chemically form the battery case due to terminal corrosion, etc., chemically formed electrode plates are generally used in small sealed lead-acid batteries.

発明の目的 本発明は、前述したように密閉形鉛蓄電池を小形化する
時に問題となる過放電放置後の充電受入性及びその後の
回復容量を向上させるとともに、電槽化成時の温液を防
止することを目的と1.だものてあ21.。
Purpose of the Invention As mentioned above, the present invention improves charge acceptance and subsequent recovery capacity after overdischarging, which is a problem when downsizing sealed lead-acid batteries, and prevents hot liquid from forming during battery cell formation. The purpose is to 1. Daemonotea 21. .

発明の構成 すなわち、本発明は前記目的を達成するため、正極板、
負極板及びガラス繊維を主成分とするセパレータよりな
る極板群に電解液を保持さぜるとともに、極板群上に保
液性を有する面1酸性多孔体を配置したことを特徴とす
るものである8このような保液性を有する耐酸性多孔体
を装備することで、ilr、j放電放置後の充電時に極
板/ffヒの多孔体よす極板へ電解液を供給して充電受
入性及びその後の回復容量を向上させることができる7
、捷だ電槽化成時におけるガス発生に伴った電解液飛沫
を捕捉し7、電池外部への温液も防止するものである。
Structure of the Invention Specifically, in order to achieve the above object, the present invention includes a positive electrode plate,
An electrode plate group consisting of a negative electrode plate and a separator mainly composed of glass fiber holds an electrolytic solution, and is characterized in that a side-1 acidic porous body having liquid retention properties is arranged on the electrode plate group. 8 By equipping an acid-resistant porous body with such liquid-retaining properties, electrolyte can be supplied to the porous body of the electrode plate/ff when charging after being left to discharge. Can improve acceptability and subsequent recovery capacity7
It captures electrolyte droplets caused by gas generation during the formation of a shattered battery, and also prevents hot liquid from leaking to the outside of the battery.

実施例の説明 以下、本発明の詳細は実施例により詳述する。Description of examples Hereinafter, the details of the present invention will be explained in detail with reference to Examples.

第2図に示す如く、正極板1.負柘板2及びガラス繊維
を主成分としたセパレータ3よりなる極板群4の上に、
とれと接触した状態で保液性を有する面1酸性多孔体5
を配置する。なお図中6は同極性極板を接続する集電側
−7は集電側6と一体に設けらり、だ極柱である。
As shown in FIG. 2, the positive electrode plate 1. On top of the electrode plate group 4 consisting of the negative oak plate 2 and the separator 3 whose main component is glass fiber,
Surface 1 Acidic porous material 5 that has liquid retaining properties when in contact with the grain
Place. In addition, in the figure, the current collecting side -7 connecting the same polarity plates is provided integrally with the current collecting side 6, and is a dipole pole.

このように構成さil−だ極板群4id、第3図に示す
如く電槽8内に挿入され、電槽蓋に設けた汁液[J兼排
気口9より電解液である希硫酸を注入し。
The electrode plate group 4id constructed in this way is inserted into the battery case 8 as shown in FIG. .

排気口9にゴム等からなる防爆安全弁10を取付けて小
形の密閉形鉛蓄電池が構成される。
A small sealed lead-acid battery is constructed by attaching an explosion-proof safety valve 10 made of rubber or the like to the exhaust port 9.

なお、極板群上に配置する耐酸性多孔体としては、ガラ
ス繊維あるいは合成樹脂繊M1を主成分とするマットか
らなり、液保持能力に優れているものが好ましい。
The acid-resistant porous body disposed on the electrode plate group is preferably made of a mat whose main component is glass fiber or synthetic resin fiber M1, and has excellent liquid retention ability.

このような電池は、極板群上に多孔体を接触させて配置
しているので、過放電後多孔体と極板群との接触面を通
じて徐々に電解液を極板に供給で・きるものである8小
形の密閉形鉛蓄電池にあ−ては、過放電した場合、電解
液量に余裕がないだめ、極板中の硫酸は完全に硫酸鉛に
変化し、極板内は中性状態になっている。そのだめ正極
格子と正極活物質との間に不導態膜が生成すると推定さ
れる。
In such batteries, the porous body is placed in contact with the electrode group, so after overdischarging, the electrolyte can be gradually supplied to the electrode plate through the contact surface between the porous body and the electrode group. 8 In the case of a small sealed lead-acid battery, if it is over-discharged, the sulfuric acid in the electrode plate will completely change to lead sulfate because there is not enough electrolyte, and the inside of the electrode plate will be in a neutral state. It has become. As a result, it is presumed that a non-conducting film is formed between the positive electrode lattice and the positive electrode active material.

このような電池は充電しようとする場合きわめて充電さ
れにくく回復容量も低い。本発明におい一〇は、過放電
した後−過放電中にはほとんど使用されなかった多孔体
中の硫酸が徐々に極板中に拡散して一正極格子と正極活
物質との間も中性状態になることはないため一不導態膜
は生成しない、そのため、過放電放置後の充電受入性及
びその後の回復容量性を向上することができた、これは
電解液を含浸した前記多孔体が極板群と密着せずに、i
p、 [接触しているだけであるだめ、過放電中にはほ
とんど硫酸は消費せずに、放置後徐々に電解液を極板に
供給できるためである。
When attempting to charge such a battery, it is extremely difficult to charge it and its recovery capacity is low. In the present invention, 10 is that after overdischarge, the sulfuric acid in the porous body, which was hardly used during overdischarge, gradually diffuses into the electrode plate, and 1) the gap between the positive electrode lattice and the positive electrode active material is also neutralized. Since the porous body impregnated with the electrolytic solution does not form a non-passive film, it is possible to improve charge acceptance after overdischarging and subsequent recovery capacity. is not in close contact with the electrode plate group, i
p, [This is because the electrolyte can be gradually supplied to the electrode plate after it is left alone, without consuming much sulfuric acid during overdischarge unless it is in contact with the electrode plate.

また、前記多孔体は未化成板を組み込んだ密閉形鉛蓄電
池に電解液を極板群の高さ以上に加え化成を行う、いわ
ゆる電槽化成時に発生する気泡が液栓下部で割り、て飛
沫が液栓部に付着することも防止することができるため
、外部への温液を防ぎ温液により起こるリークや端子腐
食を防止することができる。
In addition, the porous body is a sealed lead-acid battery that incorporates unformed plates, and the electrolyte is added to a level higher than the height of the electrode plate group to perform chemical formation, which is called battery cell formation. Air bubbles are generated at the bottom of the liquid stopper and are splashed. Since it is possible to prevent the hot liquid from adhering to the liquid stopper, it is possible to prevent the hot liquid from leaking to the outside and prevent leakage and terminal corrosion caused by the hot liquid.

今、極板の大きさを縦40mm、幅30Inm 、 J
すさは正極板で3.0 mm 、負極板でJlmmとな
るよう格子に活物質を充填し7化成したものを用い、セ
パレ成は正極板2枚、負極板3枚とし、Jii板lff
七〇・ごセパレータと同月質の1.6 clIrの多孔
体を接触σぜ。
Now, the size of the electrode plate is 40 mm in length and 30 Inn in width, J
The height of the positive electrode plate is 3.0 mm and the negative electrode plate is Jlmm.The active material is filled in the lattice and 7 chemical compositions are used, and the separate composition is 2 positive electrode plates and 3 negative electrode plates,
70. Contact the separator with a porous material of 1.6 clIr made of the same material.

比重1.30(2Q℃)の硫酸17.5mlを加えて密
閉形鉛蓄電池Aとしだ。人と同一極板群構成で、セパレ
ータと同材質の1 、t5 C1l+’のマントを極板
群下部に畜産Iさせた電池をBと−して−A、B両電池
の過放電放置後の充電受入性に依存1〜だ回復充電特性
と、その後の容量回復率とを比較した結果をそれぞれ第
4図、第5図に示す。
A sealed lead acid battery A was prepared by adding 17.5 ml of sulfuric acid with a specific gravity of 1.30 (2Q°C). A battery with the same electrode group configuration as a human being and with a cloak of 1, t5 C1l+' made of the same material as the separator placed at the bottom of the electrode group is designated as B-. The results of comparing the recovery charging characteristics and the subsequent capacity recovery rate are shown in FIGS. 4 and 5, respectively.

なお、放電は15Ω抵抗(o、sG相当、12v)で2
4h間放電とし、放置は放電後抵抗を取り除いて30日
間25℃下に置き一回復充電は147vの設定乳、圧(
2,45V/セル)−最大電流1.Ovで24時間25
℃下で充電した。
In addition, the discharge is 2 with a 15Ω resistor (o, equivalent to sG, 12V).
Discharge for 4 hours, and leave after discharging to remove the resistance and store at 25℃ for 30 days.
2,45V/cell) - maximum current 1. Ov 24 hours 25
Charged at ℃.

この第4図、第5図の比較から明らか々ように、第4図
に示す本発明の電池人の回復充電特性は充電開始後1時
間以内に急激な充電電流の増加が図れ、第6図に示す比
較電池Bに比べて短時間で回復充電重性が優れているこ
とがわかる。壕だ回復充電後の容量/初期容量x1oo
(%)で求めた容量回復率6人が90係、Bが74係で
あった一寸だ、前記寸法の未化成極板からなる極板nY
を組み込んだ電池Aおよび電池Bに電解液を21m(1
注液した後、理論必要電気量の300係を流して電槽化
成を行った。その結果人の電池には温液は全く見られず
、Bの電池はすべて温液が見られた、このととにより、
小形の電池であっても本発明の電池構成とすることによ
−で、電槽化成することが可能である、 発明の効果 このような本発明によれば、次のような効果を得ること
ができる。
As is clear from the comparison between FIGS. 4 and 5, the recovery charging characteristics of the battery according to the present invention shown in FIG. It can be seen that the recovery charge weight is superior in a short time compared to comparative battery B shown in FIG. Capacity after recovery charging/Initial capacity x1oo
The capacity recovery rate calculated by (%) was 90 for 6 people and 74 for B, a plate nY consisting of an unformed plate with the above dimensions.
21 m (1
After pouring the liquid, 300 parts of the theoretically required amount of electricity was applied to form the battery. As a result, no warm liquid was found in the human battery, and warm liquid was found in all of the B batteries.
By adopting the battery structure of the present invention, even a small battery can be made into a battery case. Effects of the Invention According to the present invention, the following effects can be obtained. I can do it.

(1)  と」tまで小形の密閉形鉛蓄電池の欠点とさ
」゛してきた過放電放置後の充電受入性とその後の回復
容量を向」ニすることができだ。
(1) It is possible to improve charge acceptance after over-discharging and subsequent recovery capacity, which have been regarded as shortcomings of small sealed lead-acid batteries.

(2)小形の密閉形鉛蓄電池は極板群と液枠部寸での距
離が短いため、温液して電槽化成が困莫1(なことから
化成した極板を使用し、できだが、極板群上に吸液性の
多孔体を配置して温液を防市できるだめ電槽化成が11
1能になった。
(2) Small sealed lead-acid batteries have a short distance between the electrode plate group and the liquid frame, so it is difficult to form a battery case using hot liquid. In 11th year, Dame Tank Kasei, which can prevent hot liquid by placing a liquid-absorbing porous body on the electrode plate group, is 11.
Became capable.

これらにより低コストで密閉形鉛蓄電池右・・jf4 
、:テ’iすることができる。
These allow low-cost sealed lead-acid batteries...jf4
, :Te'i can.

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

第1図は従来の密閉形鉛蓄電池における極板群を示す図
、第2図は本発明の実施例における極板群を示1図、第
3図は第2図の極板群を用いて構成したA発明の命閉形
鉛蓄電池の断面図、第4図は本発明の実施例における蓄
電池の回復充電特性を示すし1、第5図は従来の蓄電池
の回復充電特性−を示すし1である。 1・・・・・・正極板、2・・・・・・負極板、3・・
・・・・ガラス繊維を主成分とするセパレータ、4・・
・・・極板(jL6・・・・・・保液性を有する而」酸
性多孔体、8・・・・・電槽。
FIG. 1 is a diagram showing a plate group in a conventional sealed lead acid battery, FIG. 2 is a diagram showing a plate group in an embodiment of the present invention, and FIG. 3 is a diagram showing a plate group in an embodiment of the present invention. A cross-sectional view of the life-closed lead-acid battery according to the invention A, FIG. 4 shows the recovery charging characteristics of the storage battery according to the embodiment of the present invention, and FIG. 5 shows the recovery charging characteristics of the conventional storage battery. be. 1... Positive electrode plate, 2... Negative electrode plate, 3...
...Separator whose main component is glass fiber, 4...
...Electrode plate (jL6...Acidic porous material with liquid retention properties, 8...Battery container.

Claims (1)

【特許請求の範囲】[Claims] 上杉板、負極板及びガラス繊維を主成分とするセパレー
タよりなる極板群に電解液を保持さぜるとともに、極板
群上に保液性を有する耐酸性多孔体を配置した密閉形鉛
蓄電池。
A sealed lead-acid battery in which an electrolyte is held in an electrode plate group consisting of an Uesugi plate, a negative electrode plate, and a separator whose main components are glass fiber, and an acid-resistant porous material with liquid retention properties is arranged on the electrode plate group. .
JP57157633A 1982-09-09 1982-09-09 Enclosed lead battery Pending JPS5946771A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57157633A JPS5946771A (en) 1982-09-09 1982-09-09 Enclosed lead battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57157633A JPS5946771A (en) 1982-09-09 1982-09-09 Enclosed lead battery

Publications (1)

Publication Number Publication Date
JPS5946771A true JPS5946771A (en) 1984-03-16

Family

ID=15653980

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57157633A Pending JPS5946771A (en) 1982-09-09 1982-09-09 Enclosed lead battery

Country Status (1)

Country Link
JP (1) JPS5946771A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60207263A (en) * 1984-03-30 1985-10-18 Shin Kobe Electric Mach Co Ltd Sealed lead storage battery
JP2007230291A (en) * 2006-02-28 2007-09-13 Toshiba Logistics Corp Truck device

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60207263A (en) * 1984-03-30 1985-10-18 Shin Kobe Electric Mach Co Ltd Sealed lead storage battery
JPH0550825B2 (en) * 1984-03-30 1993-07-30 Shin Kobe Electric Machinery
JP2007230291A (en) * 2006-02-28 2007-09-13 Toshiba Logistics Corp Truck device

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