JP2921332B2 - Glass mat for lead acid battery - Google Patents

Glass mat for lead acid battery

Info

Publication number
JP2921332B2
JP2921332B2 JP5121092A JP12109293A JP2921332B2 JP 2921332 B2 JP2921332 B2 JP 2921332B2 JP 5121092 A JP5121092 A JP 5121092A JP 12109293 A JP12109293 A JP 12109293A JP 2921332 B2 JP2921332 B2 JP 2921332B2
Authority
JP
Japan
Prior art keywords
glass mat
glass
electrolyte
present
sponge
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 - Fee Related
Application number
JP5121092A
Other languages
Japanese (ja)
Other versions
JPH06333549A (en
Inventor
康司 松村
一郎 向谷
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 JP5121092A priority Critical patent/JP2921332B2/en
Publication of JPH06333549A publication Critical patent/JPH06333549A/en
Application granted granted Critical
Publication of JP2921332B2 publication Critical patent/JP2921332B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related 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

Landscapes

  • Cell Separators (AREA)
  • Secondary Cells (AREA)

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、鉛蓄電池用ガラスマッ
トに関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a glass mat for a lead storage battery.

【0002】[0002]

【従来の技術】従来、鉛蓄電池用ガラスマットは、数マ
イクロのガラス繊維を抄紙して作られており、該ガラス
繊維抄紙体の全細孔体積の80%以下が細孔径1〜10μm
であった。
2. Description of the Related Art Conventionally, glass mats for lead-acid batteries have been made by making a glass fiber of several micron, and 80% or less of the total pore volume of the glass fiber paper body has a pore diameter of 1 to 10 μm.
Met.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、このよ
うなガラス繊維抄紙体よりなるガラスマットでは、抄紙
技術に限界があり、細孔径のばらつきがある。細孔径が
ばらつくと、電解液保液率が減少し、電池性能では特に
低率放電容量が小さくなる問題点がある。
However, the glass mat made of such a glass fiber paper has a limitation in the paper making technique, and the pore diameter varies. If the pore diameter varies, the electrolyte retention rate decreases, and the battery performance has a problem that the low-rate discharge capacity is particularly small.

【0004】本発明の目的は、電解液保液率を向上でき
る鉛蓄電池用ガラスマットを提供することにある。
[0004] It is an object of the present invention to provide a glass mat for a lead-acid battery, which can improve the electrolyte retention rate.

【0005】[0005]

【課題を解決するための手段】上記の目的を達成する本
発明の構成を説明すると、本発明に係る鉛蓄電池用ガラ
スマットは、三次元的に連続した構造を有するスポンジ
状ガラス多孔体で構成され、該スポンジ状ガラス多孔体
の全細孔体積の80%以上が細孔径1〜10μmであること
を特徴とする。
The glass mat for a lead-acid battery according to the present invention comprises a porous sponge-like glass body having a three-dimensionally continuous structure. The sponge-like porous glass body is characterized in that 80% or more of the total pore volume has a pore diameter of 1 to 10 μm.

【0006】[0006]

【作用】ガラスマットの細孔径が1μmより小さくなる
と、電解液の表面張力により電解液が進入せず空間が生
じやすい。更に、ガラスマットがガラス繊維で構成され
ていると、繊維同士の交差するところは特に電解液が入
りにくい。また逆に、ガラスマットの細孔径が10μmよ
り大きくなると、電解液保持性が悪くなり、トータルの
電解液保液率が悪くなる。また、一時的に電解液を保持
しても、長時間静置していると硫酸が下降する成層化現
象が現れ、電池寿命を極端に短くする原因となる。従っ
て、ガラスマットの細孔径は、1〜10μmが最適であ
る。
When the pore size of the glass mat is smaller than 1 μm, the electrolyte does not enter due to the surface tension of the electrolyte, so that a space is easily generated. Further, when the glass mat is made of glass fiber, it is difficult for the electrolyte to enter particularly at the intersection of the fibers. Conversely, if the pore size of the glass mat is larger than 10 μm, the electrolyte retention will be poor, and the total electrolyte retention will be poor. Further, even if the electrolyte is temporarily held, a stratification phenomenon in which sulfuric acid descends appears when the electrolyte is left for a long period of time, which extremely shortens the battery life. Therefore, the pore diameter of the glass mat is optimally 1 to 10 μm.

【0007】また、細孔径1〜10μmの細孔の量につい
ては、全細孔体積の80%以上であると、電解液保液率は
ほとんど変わらず、低率放電容量も変化がないが、80%
より少なくなると、保液率が低くなり、低率放電容量も
悪くなる。
When the amount of pores having a pore diameter of 1 to 10 μm is 80% or more of the total pore volume, the electrolyte retention rate hardly changes and the low rate discharge capacity does not change. 80%
When the amount is smaller, the liquid retention rate is low, and the low rate discharge capacity is also poor.

【0008】[0008]

【実施例】以下、本発明の一実施例を詳細に説明する。
本実施例の鉛蓄電池用ガラスマット(以下、本発明品と
称する。)は、三次元的に連続した構造を有するスポン
ジ状ガラス多孔体で構成されている。このようなスポン
ジ状ガラスマットは、平均粒子径が6μmのガラスビー
ズをマット状とし、ガラスの融点近傍まで温度を上げ焼
結させることによって得られる。本発明品のスポンジ状
ガラスマットは、1〜10μmの細孔径が全細孔体積の87
%である。これに対し、従来品のガラス繊維からなるガ
ラスマットは、1〜10μmの細孔径が全細孔体積の72%
である。
DESCRIPTION OF THE PREFERRED EMBODIMENTS One embodiment of the present invention will be described below in detail.
The glass mat for a lead-acid battery (hereinafter, referred to as the present invention) of the present embodiment is formed of a sponge-like porous glass having a three-dimensionally continuous structure. Such a sponge-like glass mat is obtained by sintering glass beads having an average particle diameter of 6 μm into a mat shape, raising the temperature to near the melting point of the glass. In the sponge-like glass mat of the present invention, the pore diameter of 1 to 10 μm is 87% of the total pore volume.
%. On the other hand, the conventional glass mat made of glass fiber has a pore diameter of 1 to 10 μm of 72% of the total pore volume.
It is.

【0009】このような本発明品と従来品のガラスマッ
トとの性能比較を行った。電池はすべて4Ah−6Vタ
イプとした。
The performance of the glass mat of the present invention and that of the conventional glass mat were compared. All batteries were of the 4 Ah-6 V type.

【0010】図1は、本発明品と従来品のガラスマット
を用いた鉛蓄電池の初期容量比較である。図より、本発
明品のガラスマットを用いた鉛蓄電池は従来品のガラス
マットを用いた鉛蓄電池よりも15%高容量を示した。な
お、放電試験条件は、0.4 A放電で終止電圧1.7 V,雰
囲気条件は25±2 ℃とした。
FIG. 1 is a comparison of the initial capacities of lead storage batteries using the glass mat of the present invention and the conventional glass mat. As shown in the figure, the lead storage battery using the glass mat of the present invention exhibited 15% higher capacity than the lead storage battery using the conventional glass mat. The discharge test conditions were a 0.4 A discharge, a final voltage of 1.7 V, and the atmospheric conditions were 25 ± 2 ° C.

【0011】図2は、1〜10μmの細孔径の総体積が全
細孔体積に対する割合と保液率を示したものである。こ
れより80%以上であると、保液率はほとんど変わらず80
%より小さくなると保液率が低くなることがわかる。
FIG. 2 shows the ratio of the total volume of the pore diameters of 1 to 10 μm to the total pore volume and the liquid retention. If it is more than 80%, the liquid retention rate is almost unchanged
%, The liquid retention rate decreases.

【0012】上記実施例では、スポンジ状ガラス多孔体
の全細孔体積の87%が細孔径1〜10μmであるとした
が、本発明はこれに限定されるものではなく、スポンジ
状ガラス多孔体の全細孔体積の80%以上が細孔径1〜10
μmであればよい。
In the above embodiment, 87% of the total pore volume of the sponge-like glass porous body has a pore diameter of 1 to 10 μm. However, the present invention is not limited to this, and the present invention is not limited to this. 80% or more of the total pore volume of
μm is sufficient.

【0013】ガラスマットの細孔径が1μmより小さく
なると、電解液の表面張力により電解液が進入せず空間
が生じやすい。更に、ガラスマットがガラス繊維で構成
されていると、繊維同士の交差するところは特に電解液
が入りにくい。また逆に、ガラスマットの細孔径が10μ
mより大きくなると、電解液保持性が悪くなり、トータ
ルの電解液保液率が悪くなる。また、一時的に電解液を
保持しても、長時間静置していると硫酸が下降する成層
化現象が現れ、電池寿命を極端に短くする原因となる。
従って、ガラスマットの細孔径は、1〜10μmが最適で
ある。
When the pore size of the glass mat is smaller than 1 μm, the electrolyte does not enter due to the surface tension of the electrolyte, so that a space is easily formed. Further, when the glass mat is made of glass fiber, it is difficult for the electrolyte to enter particularly at the intersection of the fibers. Conversely, the pore size of the glass mat is 10μ.
If it is larger than m, the electrolyte retention will be poor, and the total electrolyte retention will be poor. Further, even if the electrolyte is temporarily held, a stratification phenomenon in which sulfuric acid descends appears when the electrolyte is left for a long period of time, which extremely shortens the battery life.
Therefore, the pore diameter of the glass mat is optimally 1 to 10 μm.

【0014】また、細孔径1〜10μmの細孔の量につい
ては、全細孔体積の80%以上であると、電解液保液率は
ほとんど変わらず、低率放電容量も変化がないが、80%
より少なくなると、保液率が低くなり、低率放電容量も
悪くなる。
When the amount of pores having a pore diameter of 1 to 10 μm is 80% or more of the total pore volume, the electrolyte retention rate hardly changes and the low rate discharge capacity does not change. 80%
When the amount is smaller, the liquid retention ratio is low and the low rate discharge capacity is also poor.

【0015】[0015]

【発明の効果】以上説明したように本発明に係る鉛蓄電
池用ガラスマットは、三次元的に連続した構造を有する
スポンジ状ガラス多孔体で構成され、該スポンジ状ガラ
ス多孔体の全細孔体積の80%以上が細孔径1〜10μmで
あるので、トータルの電解液保液率が高く、電池寿命が
長く、しかも低率放電特性の優れた鉛蓄電池を得ること
ができる。
As described above, the glass mat for a lead storage battery according to the present invention is composed of a sponge-like glass porous body having a three-dimensionally continuous structure, and the total pore volume of the sponge-like glass porous body. 80% or more has a pore diameter of 1 to 10 μm, so that a lead storage battery having a high total electrolyte retention rate, a long battery life, and excellent low-rate discharge characteristics can be obtained.

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

【図1】本発明品と従来品のガラスマットを用いた鉛蓄
電池の初期容量比較図である。
FIG. 1 is a comparison diagram of the initial capacities of lead storage batteries using a glass mat of the present invention and a conventional glass mat.

【図2】1〜10μmの細孔径の総体積が全細孔体積に対
する割合と保液率を示す線図である。
FIG. 2 is a diagram showing a ratio of a total volume of pore diameters of 1 to 10 μm to a total pore volume and a liquid retention ratio.

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 三次元的に連続した構造を有するスポン
ジ状ガラス多孔体で構成され、該スポンジ状ガラス多孔
体の全細孔体積の80%以上が細孔径1〜10μmであるこ
とを特徴とする鉛蓄電池用ガラスマット。
1. A sponge-like glass porous body having a three-dimensionally continuous structure, wherein 80% or more of the total pore volume of the sponge-like glass porous body has a pore diameter of 1 to 10 μm. Glass mats for lead-acid batteries.
JP5121092A 1993-05-24 1993-05-24 Glass mat for lead acid battery Expired - Fee Related JP2921332B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5121092A JP2921332B2 (en) 1993-05-24 1993-05-24 Glass mat for lead acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5121092A JP2921332B2 (en) 1993-05-24 1993-05-24 Glass mat for lead acid battery

Publications (2)

Publication Number Publication Date
JPH06333549A JPH06333549A (en) 1994-12-02
JP2921332B2 true JP2921332B2 (en) 1999-07-19

Family

ID=14802684

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5121092A Expired - Fee Related JP2921332B2 (en) 1993-05-24 1993-05-24 Glass mat for lead acid battery

Country Status (1)

Country Link
JP (1) JP2921332B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6908052B2 (en) * 2016-12-07 2021-07-21 昭和電工マテリアルズ株式会社 Liquid lead-acid battery
JP7412948B2 (en) * 2019-10-03 2024-01-15 エンテックアジア株式会社 Separator for lead acid batteries

Also Published As

Publication number Publication date
JPH06333549A (en) 1994-12-02

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