JP2855706B2 - Sealed lead-acid battery - Google Patents
Sealed lead-acid batteryInfo
- Publication number
- JP2855706B2 JP2855706B2 JP1265814A JP26581489A JP2855706B2 JP 2855706 B2 JP2855706 B2 JP 2855706B2 JP 1265814 A JP1265814 A JP 1265814A JP 26581489 A JP26581489 A JP 26581489A JP 2855706 B2 JP2855706 B2 JP 2855706B2
- Authority
- JP
- Japan
- Prior art keywords
- battery
- powder
- electrolyte
- filled
- acid
- 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
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)
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。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in a sealed lead-acid battery used for repeated charging and discharging.
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蓄電池は、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、例えば微
細ガ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使用し
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SiO2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。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浮け、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。例
えば、粒子径の小さい粉体を用いると、多孔度が小さく
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重差、いわゆる電解液
の成層化という現象が発生する。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、この硫酸鉛
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。2. Description of the Related Art Most of the sealed lead-acid batteries currently on the market are so-called retainer types, in which a positive and negative electrode plate and a separator mainly composed of fine glass fibers are impregnated and held with an electrolytic solution. Things. This closed lead storage battery of the retainer type has a problem that the cost is high, though the performance is not inferior to that of the conventional open lead storage battery. The high cost is due to the use of an expensive separator having a high liquid holding capacity, such as a fine glass fiber separator (hereinafter referred to as a glass separator), for impregnating and holding the electrolyte between the electrode plates. is there. In order to solve this cost increase, it has recently been attempted to use a powder made of an inorganic oxide such as SiO 2 instead of a glass separator or the like as an electrolyte holder. However, when powder is used, there is a drawback that the battery performance is significantly affected by the particle size of the powder, and the performance is inferior to the conventional retainer type. For example, when powder having a small particle size is used, the porosity is reduced, and not only the amount of retained electrolyte is reduced, but also the passage required for diffusion of the electrolyte is narrowed. It is significantly lower than the formula. On the other hand, if the particles of the powder used are sufficiently large, the above-mentioned drawbacks are eliminated, but the ability to retain the electrolytic solution is reduced, and the specific gravity difference in the vertical direction of the electrolytic solution when deep charge / discharge is repeated, so-called electrolytic solution A phenomenon called stratification occurs. If the battery is used in a state where the electrolyte is stratified, lead sulfate is concentrated and accumulated in the lower positive and negative plates exposed to high concentration sulfuric acid, and this lead sulfate is not activated even when charged. In addition, the capacity of the battery may be reduced. As described above, when the above-described powder is used as the electrolyte holder instead of the glass separator, performance comparable to that of the conventional retainer type battery cannot 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
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 fills the peripheral portion of the electrode plate group and the gap between the positive and negative electrode plates with an acid-resistant and oxidation-resistant powder, and absorbs the electrolytic solution into the positive and negative electrode plates and the powder. In a lead-acid battery having a holding structure, the above problem is solved by making the particle size of the powder at the bottom of the battery smaller than that at the top of the battery.
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。以下これを詳述する。Example A retainer type battery according to the present invention was manufactured and tested. This is described in detail below.
まず、高さ260mmのペースト式正極板と負極板とで構
成される極板群を作製し、これを電槽に収納した。次
に、SiO2を主成分とする粒子径の異なる粉体を2回に分
けて600g充填した。すなわち、粒子径が50〜100μ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、所定量の希硫
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2V−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およびガ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D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Dの放電容量に対する比率で示している。First, an electrode plate group including a paste-type positive electrode plate and a negative electrode plate having a height of 260 mm was prepared, and this was stored in a battery case. Next, 600 g of powder containing SiO 2 as a main component and having different particle diameters was charged in two portions. That is, after filling the lower part of the battery with 300 g of powder having a particle diameter of 50 to 100 μ, the particle diameter is 200 to 400 μ.
300 g of powder was filled thereon. Thereafter, a predetermined amount of diluted sulfuric acid is injected, and a safety valve and the like are attached according to a conventional method.
A 2V-200Ah retainer type battery A according to the present invention was obtained. Further, for comparison, a battery B filled with only powder having a particle diameter of 200 to 400 μ, a battery C filled only with powder having a particle diameter of 50 to 100 μ, and a conventional battery using a glass separator as an electrolyte holder were used. A retainer type battery D was manufactured. Table 1 shows the discharge capacities of these batteries. The values in the table are shown as ratios to the discharge capacity of the conventional retainer type battery D.
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D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 the battery A according to the present invention is inferior to that of the battery B filled only with a powder having a large particle diameter, the discharge capacity is not inferior to that of the conventional retainer type battery D even at a high rate discharge or a low rate discharge. You can see that.
一方、寿命性能については、10HR電流で端子電圧が1.
70Vになるまで放電し、続いて2.35Vで24H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B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B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A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Dに比べ
て遜色ない。本発明による電池Aで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液の成層化を防止
できる粉体の粒子径が異なり、260mm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濃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。 On the other hand, regarding the life performance, the terminal voltage is 1.
It was evaluated by a charge / discharge cycle test in which the battery was discharged to 70 V and then charged at 2.35 V for 24 hours. FIG. 1 shows the transition of the discharge capacity. From this figure, it can be seen that the capacity change of the battery B filled only with the powder having a large particle diameter is extremely poor. Table 2 shows the specific gravity difference between the electrolyte at the top and the bottom of the battery when the discharge capacity is less than 75% of the initial value. In the case of battery B, the electrolyte is significantly stratified and the life performance is low. It is considered to have decreased. In contrast,
In the battery A according to the present invention, stratification of the electrolytic solution hardly occurs, and the life performance is comparable to that of the conventional retainer type battery D. In the battery A according to the present invention, the electrolyte is not stratified because the particle size of the powder that can prevent the stratification of the electrolyte differs depending on the height of the electrode plate. It is necessary to make the diameter 50 to 100 μm, but if the height is half that, the powder having a coarser particle diameter can prevent stratification of the electrolytic solution. In other words, a powder having a large particle diameter has a weak force for holding the electrolytic solution, but as the height of the battery decreases, the force for flowing down the concentrated sulfuric acid generated during charging decreases. It is considered that the stratification can be prevented even with a coarse powder accordingly.
なお、本実施例では、粉体としての珪素の酸化物を用
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、その上に充
填する粉体の粒子径を200〜400μとしたが、この粒子径
は電池の大きさや構成および粉体の種類によって決まる
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。 In this example, silicon oxide was used as the powder, but the powder was aluminum, titanium, an oxide such as magnesium, or a mixture thereof.
The effect of the present invention is the same. Further, in this example, the particle size of the powder to be filled in the lower part of the battery was 50 to 100 μ, and the particle size of the powder to be filled thereon was 200 to 400 μ. It is determined by the type of powder. Further, in the present embodiment, the powder is filled in two stages, but it goes without saying that a battery with higher capacity and longer life can be obtained by increasing the number of times of filling (the number of stages).
発明の効果 以上述べたように、極板群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、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鉛蓄電池に
おいて、充填する粉体の粒子径を電池上部ほど大きくす
ることにより、放電容量を低下させることなく電解液の
成層化を防止できる。その結果、高容量でかつ長寿命の
大形密閉鉛蓄電池が安価で得られ、その工業的価値は甚
だ大きい。Effect of the Invention As described above, the structure in which the peripheral portion of the electrode plate group and the gap between the positive and negative electrode plates are filled with an acid-resistant and oxidation-resistant powder, and the positive and negative electrode plates and the powder absorb and hold the electrolytic solution. In the lead-acid battery having the above, the stratification of the electrolytic solution can be prevented without lowering the discharge capacity by increasing the particle size of the powder to be filled toward the upper part of the battery. As a result, a large-capacity sealed lead-acid battery having high capacity and long life can be obtained at low cost, and its industrial value is extremely large.
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す。FIG. 1 shows a battery A and other batteries B and D according to the present invention.
3 shows the transition of the discharge capacity at the time of the life test.
Claims (1)
る極板群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。An acid- and oxidation-resistant powder is filled in a peripheral portion of an electrode plate group composed of a positive and negative electrode plate and a porous separator and a gap between the positive and negative electrode plates. What is claimed is: 1. A lead-acid battery having a structure in which a body absorbs and retains an electrolyte, wherein the particle size of the powder at the bottom of the battery is smaller than that at the top 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 JPH03127464A (en) | 1991-05-30 |
| JP2855706B2 true 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) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108493494B (en) * | 2018-04-26 | 2020-04-10 | 天能集团(河南)能源科技有限公司 | Electrolyte for prolonging service life of lead-acid storage battery and preparation method thereof |
-
1989
- 1989-10-12 JP JP1265814A patent/JP2855706B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03127464A (en) | 1991-05-30 |
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