JP3221154B2 - Sealed lead-acid battery - Google Patents

Sealed lead-acid battery

Info

Publication number
JP3221154B2
JP3221154B2 JP13587393A JP13587393A JP3221154B2 JP 3221154 B2 JP3221154 B2 JP 3221154B2 JP 13587393 A JP13587393 A JP 13587393A JP 13587393 A JP13587393 A JP 13587393A JP 3221154 B2 JP3221154 B2 JP 3221154B2
Authority
JP
Japan
Prior art keywords
separator
battery
sealed lead
glass fiber
electrode plate
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 - Lifetime
Application number
JP13587393A
Other languages
Japanese (ja)
Other versions
JPH06349471A (en
Inventor
喜一 小池
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 Corp
Panasonic Holdings Corp
Original Assignee
Panasonic Corp
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 Panasonic Corp, Matsushita Electric Industrial Co Ltd filed Critical Panasonic Corp
Priority to JP13587393A priority Critical patent/JP3221154B2/en
Publication of JPH06349471A publication Critical patent/JPH06349471A/en
Application granted granted Critical
Publication of JP3221154B2 publication Critical patent/JP3221154B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、例えばポータブル機器
用として用いる密閉形鉛蓄電池に関し、特にそのセパレ
ータの改良に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a sealed lead-acid battery used, for example, for portable equipment, and more particularly to an improvement in a separator thereof.

【0002】[0002]

【従来の技術】鉛蓄電池は、他の二次電池に比較してエ
ネルギー密度が高く、安価で経済性に優れている。特に
密閉形鉛蓄電池は、最近のVTRなどの小形電子機器用
電源やバックアップ用電源としての需要が増大し、その
性能も著しく向上している。
2. Description of the Related Art A lead storage battery has a higher energy density than other secondary batteries, and is inexpensive and excellent in economy. In particular, the demand for a sealed lead-acid battery as a power supply for a small electronic device such as a VTR and a backup power supply has recently increased, and the performance thereof has been remarkably improved.

【0003】密閉形鉛蓄電池の改良に関しては、これま
で数多くの提案がなされている。その代表的なものとし
て電解液量を正極板、負極板およびセパレータからなる
極板群の孔容積(保液容積)と同等か、もしくはそれ以
下の量として、いわゆる遊離電解液(フリー液)のない
状態にして、充電末期に正極板から発生する酸素ガスを
負極板で吸収除去して、電解液量の減少を抑制する方式
が採用されている。
[0003] There have been many proposals for improvements in sealed lead-acid batteries. A typical example is a so-called free electrolyte (free solution) in which the amount of the electrolyte is equal to or less than the pore volume (retention volume) of the electrode plate group including the positive electrode plate, the negative electrode plate, and the separator. A method is adopted in which the anode gas is absorbed and removed by the negative electrode plate at the end of charging to prevent a decrease in the amount of the electrolytic solution.

【0004】この密閉形鉛蓄電池では、フリー液がない
ので、電池の使用状態を横倒しにしても、あるいは倒立
させても漏液せず、かつ補水不要であるという特徴を持
っているので、多方面に使用されている。
[0004] This sealed lead-acid battery has no free liquid, and therefore has the characteristics that it does not leak even if the battery is used upside down or even if it is turned over, and does not require water refilling. Used in the direction.

【0005】このような密閉形鉛蓄電池のセパレータ
は、保液量を向上させるため、平均直径1μm以下のガ
ラス繊維を主体とし、正極板および負極板とともに積み
重ねて極板群とされ、圧縮されて電槽に組み入れた後の
ガラス繊維密度が0.15〜0.20g/cm3 で、空
孔率93〜94%程度が一般的である。
[0005] Such a sealed lead-acid battery separator is mainly composed of glass fibers having an average diameter of 1 µm or less, and is stacked together with a positive electrode plate and a negative electrode plate to form an electrode plate group in order to improve the liquid retention amount. The glass fiber density after being incorporated in the battery case is generally 0.15 to 0.20 g / cm 3 , and the porosity is generally about 93 to 94%.

【0006】[0006]

【発明が解決しようとする課題】このような極板群のセ
パレータの構成では、セパレータの空孔率が高く保液量
が多いため、初期容量は高い値が得られる。しかし、ガ
ラス繊維密度が低いので極板との密着性が十分でなく、
高温でのトリクル充電や長期放置等で電解液が電槽表面
より蒸発し電解液が減少すると、特にセパレータ中の電
解液が減少し、セパレータと極板との密着圧力が大きく
低下する。
In such a structure of the electrode group, the separator has a high porosity and a large liquid retention amount, so that a high initial capacity can be obtained. However, since the glass fiber density is low, the adhesion to the electrode plate is not sufficient,
When the electrolytic solution evaporates from the surface of the battery case due to trickle charging at a high temperature or left for a long period of time and the amount of the electrolytic solution decreases, the electrolytic solution particularly in the separator decreases, and the adhesion pressure between the separator and the electrode plate greatly decreases.

【0007】このため、セパレータと極板の密着面積が
減少して、電池の内部抵抗が上昇するので、容量が低下
し寿命が短くなるという問題点があった。
For this reason, the contact area between the separator and the electrode plate is reduced, and the internal resistance of the battery is increased. Therefore, there is a problem that the capacity is reduced and the life is shortened.

【0008】本発明は、このような課題を解決するもの
で、電解液が減少しても、セパレータと極板との密着性
低下を防止し容量の安定化を図ることにより、長寿命の
密閉形鉛蓄電池を提供することを目的とする。
The present invention solves such a problem, and prevents a decrease in the adhesion between the separator and the electrode plate and stabilizes the capacity even if the amount of the electrolytic solution is reduced, thereby achieving a long life sealing. It is an object of the present invention to provide a lead-acid battery.

【0009】[0009]

【課題を解決するための手段】このような課題を解決す
るために、本発明の密閉形鉛蓄電池では、極板群を電槽
内に組み入れた後のセパレータのガラス繊維密度を0.
21〜0.25g/cm3 とするようにしたものであ
る。
In order to solve such a problem, in the sealed lead-acid battery of the present invention, the glass fiber density of the separator after the electrode group is incorporated in the battery case is set to 0.1.
21 to 0.25 g / cm 3 .

【0010】[0010]

【作用】このような本発明の密閉形蓄電池によれば、極
板群のセパレータのガラス繊維密度を高くすることで、
長期放置中やトリクル充電中に電解液の減少があっても
容量の低下を防止できるので、従来に比べて大幅に長寿
命化することが可能である。
According to the sealed storage battery of the present invention, by increasing the glass fiber density of the separator of the electrode group,
Even if there is a decrease in the electrolyte during long-term storage or during trickle charging, a decrease in the capacity can be prevented, so that the life can be significantly extended as compared with the conventional case.

【0011】[0011]

【実施例】以下に、本発明の一実施例の密閉形鉛蓄電池
を図面を参照しながら説明する。
DESCRIPTION OF THE PREFERRED EMBODIMENTS A sealed lead-acid battery according to one embodiment of the present invention will be described below with reference to the drawings.

【0012】本実施例に用いた密閉形鉛蓄電池は、幅2
5mm、高さ45mm、厚さ3.2mmの正極板2枚
と、厚さ1.8mmの負極板3枚、および平均繊維径が
0.8μmのバインダーを含まないで、ガラス繊維のみ
により構成され、20kg/dm2 加圧時のガラス繊維
密度が0.15g/cm3 のセパレータを交互に重ね合
わせて構成した極板群を備えたものである。これらの極
板群をABS製の電槽に組み入れ、ふたで封口して電解
液として規定量の希硫酸を注入後充電し、定格容量12
V2.0Ahの密閉形鉛蓄電池を作成した。
The sealed lead-acid battery used in this embodiment has a width of 2
5 mm, height 45 mm, thickness 3.2 mm, two positive plates, three 1.8 mm negative plates, and only glass fiber without binder having an average fiber diameter of 0.8 μm. And an electrode group formed by alternately stacking separators having a glass fiber density of 0.15 g / cm 3 when pressurized at 20 kg / dm 2 . These electrode plates were assembled in an ABS battery case, sealed with a lid, charged with a specified amount of dilute sulfuric acid as an electrolytic solution, charged, and charged to a rated capacity of 12.
A sealed lead-acid battery of V2.0 Ah was prepared.

【0013】この電池の正極板および負極板は、平均極
板厚さが±0.02mm以内になるよう選別して用い、
セパレータは、5種類の厚みの異なるものを用いて、電
槽に組み入れた後のガラス繊維密度が0.15g/cm
3 、0.18g/cm3 、0.21g/cm3 、0.2
4g/cm3 および0.27g/cm3 、空孔率が89
〜94%になるように調整した。
The positive electrode plate and the negative electrode plate of this battery are selected and used so that the average electrode plate thickness is within ± 0.02 mm.
As the separator, five types having different thicknesses were used, and the glass fiber density after being incorporated in the battery case was 0.15 g / cm.
3 , 0.18 g / cm 3 , 0.21 g / cm 3 , 0.2
4 g / cm 3 and 0.27 g / cm 3 , porosity 89
Adjusted to be ~ 94%.

【0014】このようにして作成した5種類の電池は、
充電して初期容量を測定後、40℃で13.8V定電圧
充電を行なうトリクル寿命試験に入れ、2ヶ月ごとに容
量を測定した。
The five types of batteries created in this way are:
After charging and measuring the initial capacity, the battery was subjected to a trickle life test in which the battery was charged at a constant voltage of 13.8 V at 40 ° C., and the capacity was measured every two months.

【0015】なお容量検査は、2.0Aで放電し10.
0Vまで低下するまでの時間を測定した。
In the capacity test, discharge was performed at 2.0 A.
The time until the voltage dropped to 0 V was measured.

【0016】図1には、セパレータのガラス繊維密度と
初期容量の分布の特性を示した。また、図2には、40
℃でトリクル寿命試験を行なった時の容量、内部抵抗初
期比、減液量の特性を、セパレータのガラス繊維密度別
に示した。
FIG. 1 shows the characteristics of the distribution of the glass fiber density and the initial capacity of the separator. Also, FIG.
The characteristics of the capacity, the initial ratio of the internal resistance, and the amount of liquid reduction when the trickle life test was performed at ℃ were shown for each glass fiber density of the separator.

【0017】初期容量は、セパレータのガラス繊維密度
が高くなると、従来より空孔率が2〜3%減少するた
め、セパレータの保液量が少なくなり、わずかに減少し
た。
When the glass fiber density of the separator increases, the porosity decreases by 2 to 3% as compared with the prior art, so that the liquid holding amount of the separator decreases, and the initial capacity decreases slightly.

【0018】また、40℃でのトリクル寿命特性は、従
来のガラス繊維密度0.15〜0.20g/cm3 のセ
パレータでは、5〜10ヶ月で容量が初期の50%以下
になり寿命となるが、0.21〜0.27g/cm3
ガラス繊維密度のセパレータでは、13〜20ヶ月程度
まで寿命が伸びた。トリクル充電中の電池の減液量は、
セパレータのガラス繊維密度に関係なく、トリクル充電
期間に比例して増大する。この減液により電池の内部抵
抗が増大するが、ガラス繊維密度が低い電池ほど少ない
減液量で内部抵抗が急激に上昇し早期に容量が低下する
ことがわかる。
The trickle life characteristic at 40 ° C. is such that the conventional separator having a glass fiber density of 0.15 to 0.20 g / cm 3 has a life of 5 to 10 months because the capacity becomes 50% or less of the initial value. However, the life of the separator having a glass fiber density of 0.21 to 0.27 g / cm 3 was extended to about 13 to 20 months. The amount of battery reduction during trickle charge is
It increases in proportion to the trickle charge period regardless of the glass fiber density of the separator. It can be seen that the internal resistance of the battery is increased by this liquid reduction, but the internal resistance of the battery having a lower glass fiber density increases rapidly with a small amount of liquid reduction, and the capacity decreases promptly.

【0019】この結果より、セパレータのガラス繊維密
度を従来の0.15〜0.20g/cm3 から0.21
〜0.27g/cm3 に向上させると、初期容量はわず
かに減少するが、トリクル充電での寿命を2〜3倍に伸
ばすことが可能である。
From these results, it was found that the glass fiber density of the separator was increased from the conventional 0.15 to 0.20 g / cm 3 to 0.21 g / cm 3.
When it is increased to 〜0.27 g / cm 3 , the initial capacity is slightly reduced, but the life in trickle charge can be extended to two to three times.

【0020】なお、長期放置中の電解液減少による回復
容量低下の防止にも、同じ効果が期待できる。
The same effect can be expected in preventing the recovery capacity from decreasing due to the decrease in the electrolyte during long-term storage.

【0021】しかし、セパレータのガラス繊維密度を
0.27g/cm3 にすると、極板群を電槽に組み入れ
る時の圧迫力が100kg/dm2 以上となるため、作
業性が悪くなるとともに電槽が変形しやすくなるので、
実用的には0.25g/cm3程度が上限である。
However, when the glass fiber density of the separator is 0.27 g / cm 3 , the pressing force when the electrode group is incorporated into the battery case becomes 100 kg / dm 2 or more. Is easily deformed,
Practically, the upper limit is about 0.25 g / cm 3 .

【0022】以上の実施例の説明からも明らかなよう
に、本発明の密閉形鉛蓄電池によれば、従来の電池に比
べて初期容量はわずかに低下するが、トリクル寿命は、
2〜3倍に伸びるので、長寿命で信頼性の高い電池を得
ることができる。
As is clear from the above description of the embodiment, according to the sealed lead-acid battery of the present invention, the initial capacity is slightly reduced as compared with the conventional battery, but the trickle life is increased.
Since the battery is extended two to three times, a battery having a long life and high reliability can be obtained.

【0023】この理由として、次のことが考えられる。The following can be considered as a reason for this.

【0024】セパレータのガラス繊維密度を向上させる
と、空孔率の減少によりセパレータの保液量も減少する
ので、初期容量はわずかに減少する。しかし、セパレー
タと極板の密着圧力が向上するため、トリクル充電等で
電解液が減少(特にセパレータ中の電解液)にしても、
セパレータと極板との密着面積の低下が少ないので、電
池の内部抵抗の上昇を防止でき、長寿命化が可能になる
と考えられる。
When the glass fiber density of the separator is increased, the liquid holding amount of the separator is also reduced due to the decrease in the porosity, so that the initial capacity is slightly reduced. However, since the adhesion pressure between the separator and the electrode plate is improved, even if the electrolyte decreases due to trickle charging or the like (particularly, the electrolyte in the separator),
Since the decrease in the contact area between the separator and the electrode plate is small, it is considered that the increase in the internal resistance of the battery can be prevented and the life can be extended.

【0025】[0025]

【発明の効果】以上のように、本発明によれば、極板群
のセパレータのガラス繊維密度を向上することにより、
長期放置後の容量回復性やトリクル寿命特性等を大幅に
向上できる。
As described above, according to the present invention, by improving the glass fiber density of the separator of the electrode group,
The capacity recovery after a long-term storage, the trickle life characteristic, etc. can be greatly improved.

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

【図1】本発明の一実施例における密閉形鉛蓄電池のセ
パレータのガラス繊維密度と初期容量特性を示す図であ
る。
FIG. 1 is a diagram showing glass fiber density and initial capacity characteristics of a separator of a sealed lead-acid battery according to one embodiment of the present invention.

【図2】同電池のトリクル期間と容量、内部抵抗および
減液量の関係を示す図である。
FIG. 2 is a diagram showing a relationship between a trickle period, a capacity, an internal resistance, and a liquid reduction amount of the battery.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 正極板、負極板、および平均繊維径1μ
m以下のガラス繊維のみにより実質的に構成されたセパ
レータからなる極板群を電槽に組み入れてなる密閉形鉛
蓄電池において、電槽内でのセパレータのガラス繊維密
度が0.21〜0.25g/cm3 であることを特徴と
する密閉形鉛蓄電池。
1. A positive electrode plate, a negative electrode plate, and an average fiber diameter of 1 μm.
m in a sealed lead-acid battery in which an electrode group consisting of a separator substantially composed of only glass fibers of not more than m is incorporated in a battery case, the glass fiber density of the separator in the battery case is 0.21 to 0.25 g. / Cm 3, which is a sealed lead-acid battery.
JP13587393A 1993-06-07 1993-06-07 Sealed lead-acid battery Expired - Lifetime JP3221154B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13587393A JP3221154B2 (en) 1993-06-07 1993-06-07 Sealed lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13587393A JP3221154B2 (en) 1993-06-07 1993-06-07 Sealed lead-acid battery

Publications (2)

Publication Number Publication Date
JPH06349471A JPH06349471A (en) 1994-12-22
JP3221154B2 true JP3221154B2 (en) 2001-10-22

Family

ID=15161775

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13587393A Expired - Lifetime JP3221154B2 (en) 1993-06-07 1993-06-07 Sealed lead-acid battery

Country Status (1)

Country Link
JP (1) JP3221154B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4675156B2 (en) * 2005-05-25 2011-04-20 古河電池株式会社 Control valve type lead acid battery

Also Published As

Publication number Publication date
JPH06349471A (en) 1994-12-22

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