JPS5951713B2 - sealed lead acid battery - Google Patents
sealed lead acid batteryInfo
- Publication number
- JPS5951713B2 JPS5951713B2 JP54047369A JP4736979A JPS5951713B2 JP S5951713 B2 JPS5951713 B2 JP S5951713B2 JP 54047369 A JP54047369 A JP 54047369A JP 4736979 A JP4736979 A JP 4736979A JP S5951713 B2 JPS5951713 B2 JP S5951713B2
- Authority
- JP
- Japan
- Prior art keywords
- hollow
- electrolyte
- positive
- negative electrode
- acid battery
- 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
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
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
-
- 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
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Battery Electrode And Active Subsutance (AREA)
Description
【発明の詳細な説明】
本発明は電解液を正・負極板および隔離体に保持させた
構造の所謂リテーナ式密閉形鉛蓄電池の改良に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a so-called cage-type sealed lead-acid battery having a structure in which an electrolyte is held between positive and negative electrode plates and a separator.
この種の電池Aの欠点は、第1図に示すように十分に電
解液の存在する同形の電池Bに比べて高率放電性能の劣
ることである。この原因は電解液の分布の不均一にある
。The drawback of this type of battery A is that, as shown in FIG. 1, its high rate discharge performance is inferior to that of the battery B of the same type, which has a sufficient amount of electrolyte. The cause of this is the non-uniform distribution of the electrolyte.
Bの電池では流動電解液が十分に存在するので、電解液
は均一に分布しているが、Aの電池では、正・負極活物
質および隔離体のみに電解液を含浸・保持させているだ
けであるから、電解液に対する濡れの影響を受ける。In battery B, there is a sufficient amount of fluid electrolyte, so the electrolyte is evenly distributed, but in battery A, only the positive and negative electrode active materials and the separator are impregnated with and retained electrolyte. Therefore, it is affected by wetting with the electrolyte.
すなわち隔離体、例えばガラスウールに比べて正・負極
活物質は親水性(親電解液性)が劣るので電解液は隔離
体中に多く正・負極板中には少ない状態になる。高率放
電では極板内部および極板近傍のみの電解液が使用され
るので、リテーナ式電池のように極板中の電解液の少な
いものは不利で、該電池の高率放電性能が流動電解液が
十分に存在する電池に比べて劣る原因になつている。本
発明はこのような欠点を除去し、高率放電性能のすぐれ
たリテーナ式密閉形鉛蓄電池を提供するものである。That is, since the positive and negative electrode active materials are inferior in hydrophilicity (electrolyte-philicity) compared to the separator, such as glass wool, the electrolyte is present in a large amount in the separator and in a small amount in the positive and negative electrode plates. In high-rate discharge, only the electrolyte inside and near the electrode plates is used, so batteries with a small amount of electrolyte in the plates, such as cage-type batteries, are disadvantageous, and the high-rate discharge performance of these batteries is affected by fluid electrolysis. This is the reason why the batteries are inferior to batteries with sufficient liquid. The present invention eliminates these drawbacks and provides a sealed lead-acid retainer battery with excellent high-rate discharge performance.
その要旨とするところは正・負極活物質に中空ガラス短
繊維を0.5〜10.0重量パーセント混入することで
ある。中空ガラス短繊維は両端が開口しており、中空内
に希硫を保持することができるので、そのような状態で
正・負極活物質中に存在すればリテーナ式電池の高率放
電性能の改善に有効である。すなわち高率放電において
極板中の電解液濃度は低下するが、中空内に希硫酸を含
んだガラス短繊維が活物質中に存在すると、濃度差によ
つで希硫酸が中空外に拡散して硫酸分を供給するので、
従来のリテーナ式電池に比べて高率放電がすぐれている
。The gist thereof is to mix 0.5 to 10.0 weight percent of hollow short glass fibers into the positive and negative electrode active materials. Hollow short glass fibers are open at both ends and can hold dilute sulfur inside the hollow, so if they exist in the positive and negative electrode active materials in this state, they can improve the high rate discharge performance of retainer batteries. It is effective for In other words, during high-rate discharge, the concentration of the electrolyte in the electrode plate decreases, but if short glass fibers containing dilute sulfuric acid are present in the active material inside the hollow, the dilute sulfuric acid will diffuse out of the hollow due to the concentration difference. Since the sulfuric acid content is supplied by
Superior high rate discharge compared to conventional retainer batteries.
次に実施例をもつて本発明を説明する。公称容量(2
0hR)7Ahのリテーナ式密閉形鉛蓄電池において、
正・負極活物質それぞFL&;中空ガラス短繊維を0.
5、2、5、10、15重量パーセント添加したものと
従来の無添加のものについて低温高率放電性能(28A
放電、−1℃)を比較した。Next, the present invention will be explained using examples. Nominal capacity (2
0hR) 7Ah retainer type sealed lead acid battery,
The positive and negative electrode active materials each have FL&; hollow glass short fibers of 0.
The low temperature high rate discharge performance (28A
discharge, -1°C).
その結果を表1に示す。表1で明らかなように正・負極
活物質の中空ガラス短繊維が多くなるに従つて高率放電
性能が改善された。The results are shown in Table 1. As is clear from Table 1, as the number of hollow short glass fibers in the positive and negative electrode active materials increased, the high rate discharge performance improved.
しかし添加量が15.0重量パーセントになると0.5
重量パーセントのものより低下した。これは添加量が多
いために活物質相互間の結合が切断されるためである。
したがつて添加量は0.5重量パーセントから10.0
重量パーセントの範囲にすべきである。なお、添加量が
0.5重量パーセン,卜未満になると添加による効果が
充分に得られない。また本発明に用いる中空ガラス短繊
維は電解液との濡れの点で好ましく、中空内に良好に電
解液を保持させ、また中空内から良好に電解液を滲み出
させることができる。また中空ガラス短繊維2の添加方
法は正・負極板原料の練膏時に加える希硫酸中に分散さ
せるのが好しい。そのことによつてあらかじめガラス短
繊維中空内に希硫酸を含浸させる方が含浸の容易さの点
ですぐれている。すなわち電解液の注入によつて、活物
質中に存J在するガラス短繊維の中空内に希硫酸を含浸
させる場合は、全てのガラス短繊維に均一に含浸しない
危険性がある。なお、海綿状のような複雑な形状の壁面
に多数の孔を有する微小中空体を活物質中に添加して該
こ微小中空体に電解液を保持させることも考えられるが
、このような微小中空体では中空体に含まれる電解液が
外部へ滲み出るための経路が複雑なために、中空体から
外部へ滲み出にくく、充分な効果が得られない。However, when the amount added is 15.0% by weight, 0.5
The weight percentage was lower than that of the weight percentage. This is because the bonds between the active materials are broken due to the large amount added.
Therefore, the amount added is from 0.5% by weight to 10.0% by weight.
should be in the weight percent range. Note that if the amount added is less than 0.5 weight percent, the effect of the addition will not be sufficiently obtained. Further, the hollow short glass fibers used in the present invention are preferable in terms of wettability with the electrolytic solution, and can retain the electrolytic solution well in the hollow space and allow the electrolytic solution to seep out from the hollow space well. Further, the hollow short glass fibers 2 are preferably added by dispersing them in dilute sulfuric acid added when kneading the raw materials for the positive and negative electrode plates. For this reason, impregnating the hollow glass short fibers with dilute sulfuric acid in advance is superior in terms of ease of impregnation. That is, when dilute sulfuric acid is impregnated into the hollows of the short glass fibers present in the active material by injecting the electrolytic solution, there is a risk that all the short glass fibers will not be uniformly impregnated. It is also conceivable to add microscopic hollow bodies with a large number of holes in the walls of a complicated shape such as a cavernous shape to the active material, and to have the electrolyte held in the microscopic hollow bodies. In a hollow body, the path for the electrolytic solution contained in the hollow body to seep out to the outside is complicated, so that it is difficult to seep out from the hollow body to the outside, and a sufficient effect cannot be obtained.
しかし、本発明に用いる中空ガラス短繊維はその中空が
繊維径と同心円で繊維長さに沿つた空洞で形成されてい
るので、中空の形状は単純であり、中空内の電解液は濃
度勾配に従つて容易に中空内から外部へ滲み出ることが
でき、充分な効果を発揮することができる。上述のよう
に、電解液を正・負極活物質および隔離体に含浸・保持
させた構造の所謂リテーナ式鉛蓄電池において正・負極
活物質に中空ガラス短繊維を添加すれば、高率放電性能
の改良に非常に有効であつたが、流動電解液が十分に存
在する鉛蓄電池に添加した場合も、無添加のものに比べ
て極板近傍に硫酸分が多いために高率放電性能は若干よ
くなる。However, the hollow short glass fiber used in the present invention is formed with a hollow concentric with the fiber diameter and along the length of the fiber, so the shape of the hollow is simple, and the electrolyte within the hollow is subject to a concentration gradient. Therefore, it can easily seep out from inside the hollow to the outside, and a sufficient effect can be exerted. As mentioned above, in a so-called retainer type lead-acid battery in which the electrolyte is impregnated and held in the positive and negative electrode active materials and the separator, high rate discharge performance can be improved by adding hollow glass short fibers to the positive and negative electrode active materials. Although it was very effective for improvement, even when added to a lead-acid battery with a sufficient amount of flowing electrolyte, the high rate discharge performance was slightly better compared to a battery without the addition due to the large amount of sulfuric acid near the electrode plates. .
以上のように中空ガラス短繊維を鉛蓄電池の活物質に添
加することにより高率放電性能が改善され、その工業的
価値大である。As described above, by adding hollow short glass fibers to the active material of a lead-acid battery, high rate discharge performance is improved, and this has great industrial value.
第1図は電解液が十分に存在する鉛蓄電池に比べて、電
解液を正・負極活物質および隔離体に含浸・保持させた
構造の所謂リテーナ式鉛蓄電池の高率放電性能の劣るこ
とを示す。Figure 1 shows that the high rate discharge performance of so-called retainer type lead-acid batteries, which have a structure in which positive and negative electrode active materials and separators are impregnated with and retained electrolyte, is inferior to that of lead-acid batteries that have a sufficient amount of electrolyte. show.
Claims (1)
た構造の鉛蓄電池において、正・負極板活物質中に中空
ガラス短繊維を0.5〜10.0重量パーセント添加し
たことを特徴とする密閉形鉛蓄電池。1. A lead-acid battery having a structure in which an electrolyte is impregnated and held in the positive and negative electrode plates and a separator, characterized in that 0.5 to 10.0 weight percent of hollow short glass fibers are added to the positive and negative electrode plate active materials. A sealed lead-acid battery.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP54047369A JPS5951713B2 (en) | 1979-04-17 | 1979-04-17 | sealed lead acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP54047369A JPS5951713B2 (en) | 1979-04-17 | 1979-04-17 | sealed lead acid battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS55139765A JPS55139765A (en) | 1980-10-31 |
JPS5951713B2 true JPS5951713B2 (en) | 1984-12-15 |
Family
ID=12773184
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP54047369A Expired JPS5951713B2 (en) | 1979-04-17 | 1979-04-17 | sealed lead acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5951713B2 (en) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2712400B2 (en) * | 1988-10-19 | 1998-02-10 | 松下電器産業株式会社 | Lead storage battery |
US6531248B1 (en) | 1999-10-06 | 2003-03-11 | Squannacook Technologies Llc | Battery paste |
US7159805B2 (en) | 2002-03-25 | 2007-01-09 | Evanite Fiber Corporation | Methods of modifying fibers |
US6929858B2 (en) | 2002-03-25 | 2005-08-16 | Squannacook Technologies Llc | Glass fibers |
JP4556506B2 (en) * | 2004-06-16 | 2010-10-06 | 新神戸電機株式会社 | Lead acid battery |
WO2021070231A1 (en) * | 2019-10-07 | 2021-04-15 | 昭和電工マテリアルズ株式会社 | Positive electrode plate, lead storage battery, and method for manufacturing positive electrode plate and lead storage battery |
CN115832306A (en) * | 2022-12-21 | 2023-03-21 | 湖北亿纬动力有限公司 | Electrode slurry and preparation method and application thereof |
-
1979
- 1979-04-17 JP JP54047369A patent/JPS5951713B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS55139765A (en) | 1980-10-31 |
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