JPH03127464A - Sealed type lead storage battery - Google Patents
Sealed type lead storage batteryInfo
- Publication number
- JPH03127464A JPH03127464A JP1265814A JP26581489A JPH03127464A JP H03127464 A JPH03127464 A JP H03127464A JP 1265814 A JP1265814 A JP 1265814A JP 26581489 A JP26581489 A JP 26581489A JP H03127464 A JPH03127464 A JP H03127464A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- battery
- filled
- electrode plates
- 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.)
- Granted
Links
Classifications
-
- 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
- Secondary Cells (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は充電と放電とが繰り返される用途の密閉式鉛蓄
電池の改良に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to an improvement in a sealed lead-acid battery for use in which charging and discharging are repeated.
従来の技術とその課題
現在市販されている密閉式鉛蓄電池の大部分は、正負極
板と微細ガラス繊維を主成分とする隔離体とに電解液を
含浸・保持させた、いわゆるリテーナ式と呼ばれるもの
である。このリテーナ式密閉鉛M電池は、従来の開放式
の鉛蓄電池に比べて、性能面では遜色はないもののコス
トが高いという問題点を有している。コスト高の原因は
、極板間に電解液を含浸・保持するために、関えば微細
カラス繊維セパレータ(以後ガラスセパレータと呼ぶ〉
等の液保持能力の優れた高価なセパレータを代用してい
るためである。このコスト高を解消するために、最近電
解液保持体として、ガラスセパレータなどの代わりにS
i 02などの無機酸化物から成る粉体を用いることが
試みられている6しかし、粉体を用いた場合には、電池
性能が粉体の粒子径によって著しい影響を受け、しかも
性能面で従来のリテーナ式より劣るという欠点がある。Conventional technology and its issues Most of the sealed lead-acid batteries currently on the market are of the so-called retainer type, in which the positive and negative electrode plates and a separator mainly composed of fine glass fibers are impregnated and held with an electrolyte. It is something. Although this cage-type sealed lead-acid M battery is comparable in performance to conventional open-type lead-acid batteries, it has the problem of high cost. The reason for the high cost is the use of fine glass fiber separators (hereinafter referred to as glass separators) to impregnate and retain the electrolyte between the electrode plates.
This is because expensive separators with excellent liquid holding capacity such as In order to eliminate this high cost, S
Attempts have been made to use powders made of inorganic oxides such as i026. However, when using powders, battery performance is significantly affected by the particle size of the powder, and the performance The disadvantage is that it is inferior to the retainer type.
例えば、粒子径の小さい粉体を用いると、多孔度か小さ
くなり、電解液の保持量が少なくなるだけでなく、電解
液の拡散に必要な通路が細くなるために、放電性能は従
来のリテーナ式に比べて著しく低下する。これに対し、
用いる粉体の粒子を充分に大きくすると上記の欠点はな
くなるが、電解液の保持能力が低下し、深い充放電を繰
り返し行うと電解液の上下方向の比jf5差、いわゆる
電解液の成層化という現象が発生ずる。電解液が成層化
した状態で電池が使用されると、高濃度硫酸にさらされ
た下部の正負極板中に硫酸鉛が集中して蓄積され、この
硫B 3’aは充電しても活性化されないために、電池
の容量低下の原因となる。このように、上述した粉体を
ガラスセパレータの代わりに電解液保持体として用いる
と、従来のリテーナ式電池に比べて遜色のない性能を得
ることができなかった。For example, if a powder with a small particle size is used, the porosity becomes smaller, which not only reduces the amount of electrolyte retained, but also narrows the passageway required for electrolyte diffusion, so the discharge performance is lower than that of a conventional retainer. This is significantly lower than the formula. In contrast,
If the particles of the powder used are made sufficiently large, the above disadvantages will disappear, but the electrolyte retention capacity will decrease, and repeated deep charging and discharging will cause a difference in the ratio jf5 in the vertical direction of the electrolyte, so-called stratification of the electrolyte. A phenomenon occurs. When a battery is used with a stratified electrolyte, lead sulfate concentrates and accumulates in the lower positive and negative electrode plates exposed to high concentration sulfuric acid, and this sulfur B3'a remains active even after charging. This causes a decrease in battery capacity. As described above, when the above-mentioned powder is used as an electrolyte holder instead of a glass separator, performance comparable to that of conventional retainer batteries could not be obtained.
課題を解決するための手段
本発明は、極板群の周辺部および正負極板間の間隙に画
成・画成化性の粉体を充填し、該正負極板と該粉体に電
解液を吸収、保持させる構造を有する鉛蓄電池において
、電池下部の該粉体の粒子径を電池上部に比べて小さく
することにより、上記問題点を解決するものである。Means for Solving the Problems The present invention is characterized in that the periphery of a group of electrode plates and the gap between the positive and negative electrode plates are filled with a defining/defining powder, and the positive and negative electrode plates and the powder are filled with an electrolytic solution. The above problem is solved by making the particle size of the powder in the lower part of the battery smaller than that in the upper part of the battery in a lead-acid battery having a structure that absorbs and retains .
実施例 本発明によるリテーナ式電池を製作し、試験を行った。Example A retainer type battery according to the present invention was manufactured and tested.
以下これを詳述する。This will be explained in detail below.
よす、高さ260rr1mのペースト式正極板ど負榛板
とで構成される極板群を作製し、これを電槽に収納l−
た。次に、Si O□を主成分とする粒子径の異なる粉
体を2回に分けてeoog充填した。すなわち、粒子径
が50へ一100μの粉体300gを電池の下部に充填
した後、粒子径が200〜400μの粉体300gをそ
の上に充填した。この後、所定量のS硫酸を注入し、常
法にしたがって安全弁などを装着して、本発明による2
V −200Ahのリテーナ式電池Aを得た。また、
比較のために粒子径が200〜400μの粉体のみを充
填した電池B、粒子径が50〜100μの粉体のみを充
填した電池Cおよびカラスセパレータを電解液保持体に
用いた従来のリテーナ式電池りを作製した。これらの電
池の放電容量を第1表に示す。表中の値は、従来のリテ
ーナ式電池りの放電界−址に対する比率で示している。OK, I made a group of electrode plates consisting of a paste-type positive electrode plate and a shank plate with a height of 260rr1m, and stored this in a battery case.
Ta. Next, powders containing SiO□ as a main component and having different particle sizes were filled into the eoog in two parts. That is, after filling the lower part of the battery with 300 g of powder having a particle size of 50 to 100 μm, 300 g of powder having a particle size of 200 to 400 μm was filled thereon. After that, a predetermined amount of S sulfuric acid is injected, a safety valve etc. are attached according to the usual method, and the
A retainer type battery A of V-200Ah was obtained. Also,
For comparison, battery B is filled only with powder with a particle size of 200 to 400 μm, battery C is filled with only powder with a particle size of 50 to 100 μm, and a conventional retainer type using a glass separator as an electrolyte holder. A battery was made. Table 1 shows the discharge capacities of these batteries. The values in the table are expressed as a ratio to the discharge field of a conventional retainer type battery.
本発明による電池Aの放電容量は、粒子径の大きい粉体
のみを充填した電池Bに比べると劣るものの、従来のリ
テーナ式電池りに比べると高率放電でも、低率放電でも
、遜色のないことがわかる。Although the discharge capacity of battery A according to the present invention is inferior to battery B, which is filled only with powder having a large particle size, it is comparable in both high rate discharge and low rate discharge compared to conventional retainer type batteries. I understand that.
第1表
一方、寿命性能については、10 HR電流で端子電圧
が1.70Vになるまで放電し、続いて2.35Vで2
411充電するという充放電サイクル試験により評価し
た。放電容量の推移を第1図に示す。この図より、粒子
径が大きい粉体のみを充填した電池F3の容量推移が極
めて悪いことがわかる。放電容量が初期のそれの75%
を切った時点における電池上部と電池下部の電解液の比
重差を第2表に示すが、電池口では電解液が著しく成層
化しており、このため寿命性能が低下したものと考えら
れる。これに対し、本発明による電池へでは、電解液の
成層化はほとんど起っておらず、寿命性能も従来のリテ
ーナ式電池りに比べて遜色ない。本発明による電池A″
C−電解液が成層化しないのは、極板の背の高さによっ
て電解)&の成層化を防止できる粉体の粒子径が異なり
、26OIIll′fiの高さであれば粉体の粒子径を
50〜100μにする必要があるが、その半分の高さで
あればそれより粗い粒子径の粉体で電解液の成層化が防
止できるからである。すなわち、粒子径の大きな粉体は
電解液を保持する力は弱いが、電池の背が低くなるほど
、充電時に生成される漂厚な硫酸の流下しようとする力
は小さくなるので、電池の背の高さに応じて粗い粉体で
も成層化が防止できるということになると考えられる。Table 1 On the other hand, regarding life performance, discharge at 10 HR current until the terminal voltage reaches 1.70V, then discharge at 2.35V for 2 hours.
It was evaluated by a charge/discharge cycle test in which the battery was charged at 411 times. Figure 1 shows the change in discharge capacity. From this figure, it can be seen that the capacity change of battery F3 filled only with powder having a large particle size is extremely poor. Discharge capacity is 75% of initial value
Table 2 shows the difference in specific gravity between the electrolyte at the top of the battery and the bottom of the battery at the time when the battery was turned off.The electrolyte was significantly stratified at the battery mouth, which is thought to be the reason for the decrease in life performance. On the other hand, in the battery according to the present invention, there is almost no stratification of the electrolyte, and the life performance is comparable to that of conventional retainer type batteries. Battery A″ according to the invention
C- The reason why the electrolytic solution does not become stratified is that the particle size of the powder that can prevent stratification varies depending on the height of the electrode plate, and if the height is 26OIIll'fi, the particle size of the powder It is necessary to set the height to 50 to 100 μm, but if the height is half that height, stratification of the electrolyte solution can be prevented with powder having a coarser particle size. In other words, powder with a large particle size has a weak ability to hold the electrolyte, but the shorter the battery, the less force the thick sulfuric acid produced during charging will have to flow down. It is thought that stratification can be prevented even with coarse powder depending on the height.
第2表
なお、本実施例では、粉本としてのI1素の酸化物を用
いたが、粉体がアルミニウム、チタニウム、マグネシウ
ムなどの酸化物、あるいはそれらの混合物であっても、
本発明の効果は同じである。また、本実施例では、電池
下部に充填する粉体の粒子径を50〜100μ、その」
二に充填する粉体の粒子径を200〜400 JZとし
たが、この粒子径は電池の大きさや柘成および粉体の秤
類によって決まるものである。さらに、本実施例では、
二段階に分けて粉体を充填したが、充填回数(段回数)
を増やせば、より高容量で、かつ長寿命の電池が得られ
ることはいうまでもない。Table 2 Note that in this example, an oxide of I1 element was used as the powder, but even if the powder is an oxide of aluminum, titanium, magnesium, etc., or a mixture thereof,
The effect of the present invention is the same. In addition, in this example, the particle size of the powder filled in the lower part of the battery was 50 to 100 μm.
The particle size of the powder to be filled in the second cell was set to 200 to 400 JZ, but this particle size is determined by the size of the battery, the size of the battery, and the scale of the powder. Furthermore, in this example,
Powder was filled in two stages, but the number of times of filling (number of stages)
It goes without saying that by increasing the number of cells, a battery with higher capacity and longer life can be obtained.
発明の効果
以上述べたように、極板群の周辺部および正n極板間の
間隙に耐酸・1Ift酸化性の粉体を充填し、正負極板
と粉体に電解液を吸収、保持させる構造を有する3;1
蓄電池において、充填する粉体の粒子径を電池上部はど
大きくすることにより、放電容量を低′「さぜることな
く電解液の成I鍔化を防止できる。その結果、高容量で
かつ長寿命の大形密閉3rE’、蓄電池が安価で得られ
、その工業的価値は甚だ大きい。Effects of the Invention As described above, the peripheral part of the electrode plate group and the gap between the positive and n electrode plates are filled with acid-resistant and 1 Ift oxidation powder, and the electrolyte is absorbed and retained by the positive and negative electrode plates and the powder. 3;1 with structure
In storage batteries, by increasing the particle size of the powder to be filled in the upper part of the battery, it is possible to reduce the discharge capacity and prevent the formation of electrolyte without stirring. A large, sealed storage battery with a long life of 3rE' can be obtained at low cost, and its industrial value is enormous.
第1図は、 本発明による電池Aおよびその他の 電池B。 Dの寿命試験時における放電容量の推移を示ず。 Figure 1 shows Battery A according to the invention and other Battery B. The change in discharge capacity during the life test of D is not shown.
Claims (1)
の周辺部および正負極板間の間隙に耐酸・耐酸化性の粉
体を充填し、該正負極板と該粉体に電解液を吸収、保持
させる構造を有する鉛蓄電池において、電池下部の該粉
体の粒子径を電池上部に比べて小さくしたことを特徴と
する密閉式鉛蓄電池。1. Fill the periphery of the electrode plate group consisting of positive and negative electrode plates and porous separators and the gap between the positive and negative electrode plates with acid- and oxidation-resistant powder, and electrolyze the positive and negative electrode plates and the powder. A sealed lead acid battery having a structure for absorbing and retaining liquid, characterized in that the particle size of the powder in the lower part of the battery is smaller than that in the upper part of the battery.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1265814A JP2855706B2 (en) | 1989-10-12 | 1989-10-12 | Sealed lead-acid battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1265814A JP2855706B2 (en) | 1989-10-12 | 1989-10-12 | Sealed lead-acid battery |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03127464A true JPH03127464A (en) | 1991-05-30 |
| JP2855706B2 JP2855706B2 (en) | 1999-02-10 |
Family
ID=17422425
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1265814A Expired - Lifetime JP2855706B2 (en) | 1989-10-12 | 1989-10-12 | Sealed lead-acid battery |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2855706B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108493494A (en) * | 2018-04-26 | 2018-09-04 | 天能集团(河南)能源科技有限公司 | A kind of electrolyte and its compound formulation improving lead-acid accumulator service life |
-
1989
- 1989-10-12 JP JP1265814A patent/JP2855706B2/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108493494A (en) * | 2018-04-26 | 2018-09-04 | 天能集团(河南)能源科技有限公司 | A kind of electrolyte and its compound formulation improving lead-acid accumulator service life |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2855706B2 (en) | 1999-02-10 |
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