JPH02174072A - Lead-acid battery - Google Patents

Lead-acid battery

Info

Publication number
JPH02174072A
JPH02174072A JP63332956A JP33295688A JPH02174072A JP H02174072 A JPH02174072 A JP H02174072A JP 63332956 A JP63332956 A JP 63332956A JP 33295688 A JP33295688 A JP 33295688A JP H02174072 A JPH02174072 A JP H02174072A
Authority
JP
Japan
Prior art keywords
battery
electrode plate
thickness
electrolyte
separator
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.)
Pending
Application number
JP63332956A
Other languages
Japanese (ja)
Inventor
Takao Ozaki
隆生 尾崎
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 Holdings Corp
Original Assignee
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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP63332956A priority Critical patent/JPH02174072A/en
Publication of JPH02174072A publication Critical patent/JPH02174072A/en
Pending 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
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Landscapes

  • Secondary Cells (AREA)

Abstract

PURPOSE:To extract a stable capacity over a long period by making a positive electrode plate and a negative electrode plate thinner in thickness at the upper section in the installation direction of a storage battery than at the lower section. CONSTITUTION:A positive electrode plate 1 and a negative electrode plate 2 are made thinner in thickness at the upper section in the installation direction of a battery than at the lower section into a structure with a trapezoidal longitudinal section, and positive electrode plates 1, negative electrode plates 2 and separators 3 with uniform thickness are combined and inserted into a battery jar 4 to form a storage battery. The quantity of the electrolyte held in the separator 3 is proportional to the apparent volume of the separator 3 if the material and characteristic are the same, the separator 3 is made thicker in thickness by the quantity that the positive electrode plate 1 and the negative electrode plate 2 are made thinner in thickness, and the apparent volume is increased. The electrolyte holding strength is sharply increased, and the movement of the electrolyte can be blocked.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、特に蓄電池の保守軽減が重要な機器、あるい
は蓄電池から発生する希硫酸分を含んだ酸化性のガス(
以後酸霧という)が傷害となるような機器、場所での利
用に適する鉛蓄電池に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is particularly applicable to equipment in which it is important to reduce the maintenance of storage batteries, or to oxidizing gas (containing dilute sulfuric acid) generated from storage batteries.
This relates to lead-acid batteries suitable for use in equipment and locations where acid fog (hereinafter referred to as acid fog) may cause injury.

従来の技術 鉛蓄電池は比較的安価な電源として様々な用途に利用さ
れてきたが、その特性上、誰もが簡単に取り扱えるまで
には至っていない。その理由としているいろ上げられる
が、1つには電解液として希硫酸を用いており蓄電池が
損傷したときなど電解液が流れ出ること、また正常な使
用状態であっても充電中に希硫酸分を含んだ酸霧が発生
して周辺の機器、あるいは環境を汚染する事が上げられ
る。
Conventional technology Lead-acid batteries have been used for a variety of purposes as a relatively inexpensive power source, but due to their characteristics, not everyone can use them easily. There are many reasons for this, but one reason is that dilute sulfuric acid is used as the electrolyte, and the electrolyte may flow out when the battery is damaged, and even under normal usage conditions, dilute sulfuric acid may Containing acid mist may be generated and contaminate surrounding equipment or the environment.

従来から蓄電池より発生する酸霧を取り除くために、例
えば触媒を使って充電時に発生する酸素ガスと水素ガス
を反応させて水として蓄電池内に戻す方法などが、ひろ
く用いられている。
Conventionally, in order to remove acid mist generated from storage batteries, methods have been widely used, such as using a catalyst to cause the oxygen gas and hydrogen gas generated during charging to react and return the mixture as water into the storage battery.

また、最近では鉛蓄電池の次の様な特性を利用して蓄電
池を密閉する方式が増えてきた。すなわち鉛蓄電池を充
電するとまず最初に陽極より酸素ガスが発生し、その後
しばらくして陰極より水素ガスが発生し始める。よって
充電条件を適当に選ぶことによってほとんど酸素ガスし
か発生しない領域で蓄電池を充電することができる。こ
の時発生した酸素ガスは陰極板の反応物質である金属鉛
と反応(酸素ガス吸収反応)させ消費することでセル内
部の圧力上昇を防ぐことができる。
Furthermore, recently, there has been an increase in the number of methods for sealing storage batteries by taking advantage of the following characteristics of lead-acid batteries. That is, when a lead-acid battery is charged, oxygen gas is first generated from the anode, and then hydrogen gas begins to be generated from the cathode after a while. Therefore, by appropriately selecting the charging conditions, it is possible to charge the storage battery in a region where almost only oxygen gas is generated. The oxygen gas generated at this time reacts with metal lead, which is a reactant of the cathode plate (oxygen gas absorption reaction), and is consumed, thereby preventing a rise in pressure inside the cell.

以上の様な特性を利用して密閉式、あるいはシール式と
呼ばれる鉛蓄電池が最近多く製造されるようになってき
た。
Taking advantage of the above-mentioned characteristics, many sealed type or sealed type lead-acid batteries have recently been manufactured.

密閉式鉛蓄電池は酸素ガス吸収反応を利用したセル内圧
防止機構を備えるとともに、電解液の量を少なくし、し
かも電解液が流動するのを防ぐため微細なガラス繊維な
どからなる多孔性の材料にこれを吸収、保持させる構造
を備えている。
Sealed lead-acid batteries are equipped with a cell internal pressure prevention mechanism that uses oxygen gas absorption reactions, and are made of porous materials such as fine glass fibers to reduce the amount of electrolyte and prevent the electrolyte from flowing. It has a structure that absorbs and retains this.

この様な構造を備えた密閉式鉛蓄電池は有害な酸霧を発
生しない、また蓄電池を転倒しても電解液である希硫酸
が外部に流れ出ないということから最近ではひろく電子
機器の電源として用いられるようになってきた。
Sealed lead-acid batteries with this type of structure do not generate harmful acid mist, and even if the battery is tipped over, the electrolyte (dilute sulfuric acid) does not flow out, so it has recently been widely used as a power source for electronic devices. It has become possible to do so.

発明が解決しようとする課題 上記のごとく密閉式鉛蓄電池では電解液のほとんどが電
解液保持体く以後セパレータとする。)に吸収、保持さ
れているので蓄電池の性能はセパレータによって大部分
法まってしまう。
Problems to be Solved by the Invention As mentioned above, in a sealed lead-acid battery, most of the electrolyte is contained in the electrolyte holder and then the separator. ), the performance of the storage battery is largely determined by the separator.

しかしながら従来の密閉式蓄電池ではセパレータが一連
となっているため上部に保持されている電解液は充放電
の繰り返し、あるいは時間の経過とともに重力によって
徐々に下部に移行する。この結果セパレータ上部では電
解液の量が著しく減少する。さらに電解液中の硫酸分は
電解液のもう1つの成分である水に比べて比重が大きい
ため、セパレータの下部に集まり易くその結果下部では
硫酸濃度が上昇、上部では低下する。
However, since conventional sealed storage batteries have a series of separators, the electrolyte held in the upper part gradually moves to the lower part due to repeated charging and discharging or due to gravity over time. As a result, the amount of electrolyte in the upper part of the separator is significantly reduced. Furthermore, since the sulfuric acid content in the electrolytic solution has a higher specific gravity than water, which is another component of the electrolytic solution, it tends to collect at the lower part of the separator, and as a result, the sulfuric acid concentration increases in the lower part and decreases in the upper part.

この様な現象が生ずると極板の上部では電池反応に必要
な電解液が不足し、かつセパレータ部の電気抵抗が大き
くなるため電池容量は著しく減少し電池の寿命が短くな
る。また下部では電解液が豊富にあるために容量として
は十分にあるが、充放電の繰り返しにより次第に電解液
濃度が高くなり格子の腐食、活物質の不活性かが促進さ
れるという問題点があった。
When such a phenomenon occurs, there is a shortage of electrolyte necessary for the battery reaction in the upper part of the electrode plate, and the electrical resistance of the separator portion increases, resulting in a significant decrease in battery capacity and shortening of battery life. In addition, although there is sufficient electrolyte in the lower part, there is a problem that the electrolyte concentration gradually increases due to repeated charging and discharging, which accelerates corrosion of the lattice and deactivation of the active material. Ta.

課題を解決するための手段 この問題点を解決するために本発明よりなる蓄電池では
、電池設置方向に対して陽極板と陰極板の上部の厚みを
下部よりも薄くして台形状の縦断面を有する構造とする
。このようにした陽極板、陰極板と均一な厚みのセパレ
ータを組み合わせて電槽に挿入し蓄電池とする。
Means for Solving the Problem In order to solve this problem, in the storage battery according to the present invention, the thickness of the upper part of the anode plate and the cathode plate is made thinner than the lower part with respect to the battery installation direction, so that a trapezoidal vertical cross section is formed. The structure is as follows. The anode plate, the cathode plate, and a separator of uniform thickness are combined and inserted into a battery case to form a storage battery.

作用 セパレータ中に保持される電解液量は、材質、特性が同
じであればセパレータの見掛は体積に比例する。よって
上記のような手段を取ることによって極板の上部では下
部に比べて陽極板、陰極板の厚みが薄い分だけセパレー
タの厚みが厚くなり見掛は体積が増える。その結果、電
解液保持力も著しく増大し電解液の移動を阻止できる。
Effect The amount of electrolyte held in the separator is proportional to the volume of the separator if the material and properties are the same. Therefore, by taking the above-mentioned measures, the separator becomes thicker in the upper part of the electrode plate by the amount that the anode plate and the cathode plate are thinner than in the lower part, and the apparent volume increases. As a result, the electrolyte holding power increases significantly, and movement of the electrolyte can be prevented.

実施例 本発明による鉛蓄電池の断面図を第1図に示す。図中1
は陽極板、2は陰極板、3はセパレータ、4は電槽であ
る。陽極板は上部の厚みが2m下部の厚みが3m、陰極
板は上部の厚みが1.5m下部の厚みが2.0+aであ
る。
EXAMPLE A sectional view of a lead-acid battery according to the present invention is shown in FIG. 1 in the diagram
is an anode plate, 2 is a cathode plate, 3 is a separator, and 4 is a battery case. The anode plate has a thickness of 2 m at the top and 3 m at the bottom, and a cathode plate has a thickness of 1.5 m at the top and 2.0+a at the bottom.

セパレータ3はガラスあるいは合成樹脂の微細な繊維を
多数しよう造したものであり通常繊維径として0.1〜
10ミクロンのものを用いる。繊維同士のからまりを助
け、型くずれを防ぐために小量のバインダを用いること
もある。また電解液の漏れ性を向上するために繊維の表
面は界面活性材で処理する。
The separator 3 is made of many fine fibers of glass or synthetic resin, and the fiber diameter is usually 0.1~
A 10 micron one is used. A small amount of binder is sometimes used to help the fibers tangle with each other and prevent them from losing their shape. Additionally, the surface of the fibers is treated with a surfactant to improve leakage of the electrolyte.

本実施例ではセパレータの厚みは20kg/dm2加圧
時で2.5柵としている。
In this embodiment, the thickness of the separator is 2.5 mm when a pressure of 20 kg/dm2 is applied.

1セルあたりの極板構成枚数は陽極板4枚。The number of electrode plates per cell is 4 anode plates.

陰極板5枚、セパレータ8枚とし、これらを幅34.2
nnのセルに挿入して、20時間率容量52Ahの蓄電
池としている。
5 cathode plates and 8 separators, with a width of 34.2
It is inserted into a nn cell to create a storage battery with a 20 hour rate capacity of 52Ah.

本発明の効果を明らかにするため比較電池として従来の
蓄電池(陽極板の厚さ2 、5 mm 、陰極板の厚さ
1.75m+n、セパレータの厚さ2 、5 mmより
なる電池)を用いて次の様な試験を実施した。蓄電池の
容量は初期に於いていずれも52Ahである。
In order to clarify the effects of the present invention, a conventional storage battery (a battery consisting of an anode plate with a thickness of 2.5 mm, a cathode plate with a thickness of 1.75 m+n, and a separator thickness of 2.5 mm) was used as a comparative battery. The following tests were conducted. The initial capacity of each storage battery is 52 Ah.

本実施例による蓄電池と比較蓄電池を25±2℃の雰囲
気温度に置いて20時間率電流に相当する2、6Aで蓄
電池電圧が10.2Vになるまで放電をする。
The storage battery according to this example and the comparative storage battery were placed at an ambient temperature of 25±2° C. and discharged at 2.6 A corresponding to a 20 hour rate current until the battery voltage reached 10.2V.

その後、5.2への電流で放電電気量の120%の電気
量を充電する。この放電、充電を1サイクルとしてさら
にサイクルを繰り返し、蓄電池容量が定格容量の50%
以下に至った時点で終了した。
Thereafter, 120% of the amount of electricity discharged is charged with the current to 5.2. This discharging and charging cycle is repeated further, and the storage battery capacity reaches 50% of the rated capacity.
It ended when the following was reached.

この試験の結果を第2図に示した。The results of this test are shown in FIG.

同図かられかる通り比較蓄電池では150サイクルの時
点で容量が50%以下になったが、本実施例からなる蓄
電池では150サイクル時点で容量は47Ahであり、
容量が50%以下となるのは325サイクルである。
As can be seen from the figure, the comparative storage battery had a capacity of 50% or less at the 150th cycle, but the storage battery of this example had a capacity of 47Ah at the 150th cycle.
It takes 325 cycles for the capacity to decrease to 50% or less.

また本実施例よりなる蓄電池と比較蓄電池を25±2℃
の雰囲気に6力月間放置しその後5.2Aで3時間補充
電をして容量の測定を行った。その結果を第3図にまと
めた。この結果より本発明よりなる蓄電池では比較蓄電
池に比べて容量がはるかに大きくなっている。
In addition, the storage battery of this example and the comparative storage battery were heated at 25±2°C.
The battery was left in an atmosphere for 6 months, then supplementary charged at 5.2A for 3 hours, and the capacity was measured. The results are summarized in Figure 3. The results show that the storage battery according to the present invention has a much larger capacity than the comparative storage battery.

発明の効果 以上のように本発明からなる鉛蓄電池にあっては従来の
鉛蓄電池に比べて使用中、あるいは放置中の蓄電池容量
の低下が著しく少なく長期に渡って安定した容量を取り
出すことが可能となる。
Effects of the Invention As described above, in the lead-acid battery of the present invention, the decrease in battery capacity during use or storage is significantly less than in conventional lead-acid batteries, and it is possible to obtain stable capacity over a long period of time. becomes.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の一実施例より成る鉛蓄電池の断面図、
第2図は本実施例よりなる鉛蓄電池と従来の鉛蓄電池を
比較した寿命特性図、第3図は本実施例よりなる鉛蓄電
池と従来の鉛蓄電池の放置後の容量を比較した説明図で
ある。 1・・・・・・陽極板、2・・・・・・陰極板、3・・
・・・・セパレータ。 代理人の氏名 弁理士 粟野重孝 ほか1名1−一腸極
板 2−・電極板 3゛°゛セハ0レーク 第2図 充かν睨!数、
FIG. 1 is a sectional view of a lead-acid battery according to an embodiment of the present invention;
Fig. 2 is a life characteristic diagram comparing the lead-acid battery according to this embodiment and a conventional lead-acid battery, and Fig. 3 is an explanatory diagram comparing the capacity of the lead-acid battery according to this embodiment and a conventional lead-acid battery after being left unused. be. 1... Anode plate, 2... Cathode plate, 3...
...Separator. Name of agent: Patent attorney Shigetaka Awano and 1 other person 1-Inchal electrode plate 2-・Electrode plate 3゛°゛Seha 0 Lake Figure 2 Mitsuka ν glare! number,

Claims (1)

【特許請求の範囲】[Claims] 陽極板と、陰極板と、前記両極板間に介在し希硫酸を主
体とする電解液を流動しないように保持する電解液保持
体とよりなる密閉式鉛蓄電池にあって、前記陽極板およ
び陰極板は、蓄電池設置方向上部の極板厚みを下部より
も薄くしたことを特長とする鉛蓄電池。
A sealed lead-acid battery comprising an anode plate, a cathode plate, and an electrolyte holder that is interposed between the two electrode plates and holds an electrolyte mainly composed of dilute sulfuric acid so that it does not flow, the anode plate and the cathode. The board is a lead-acid battery that is characterized by the thickness of the upper electrode plate being thinner than the lower part in the direction of battery installation.
JP63332956A 1988-12-27 1988-12-27 Lead-acid battery Pending JPH02174072A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63332956A JPH02174072A (en) 1988-12-27 1988-12-27 Lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63332956A JPH02174072A (en) 1988-12-27 1988-12-27 Lead-acid battery

Publications (1)

Publication Number Publication Date
JPH02174072A true JPH02174072A (en) 1990-07-05

Family

ID=18260694

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63332956A Pending JPH02174072A (en) 1988-12-27 1988-12-27 Lead-acid battery

Country Status (1)

Country Link
JP (1) JPH02174072A (en)

Similar Documents

Publication Publication Date Title
US20080113268A1 (en) Recombinant Hybrid Energy Storage Device
JP3952483B2 (en) Sealed lead acid battery
JP2004055323A (en) Control valve type lead-acid battery
JP2004014283A (en) Valve regulated lead battery
JPH0756811B2 (en) Sealed lead acid battery
JPH02174072A (en) Lead-acid battery
JP2949839B2 (en) Negative gas absorption sealed lead-acid battery
JPS61165956A (en) Sealed type lead acid battery
US3457111A (en) Alkaline storage battery with be(oh)2 in the electrolyte
JPH04296464A (en) Sealed-type lead-acid battery
JPH0628169B2 (en) Sealed lead acid battery
JPS6040672B2 (en) Manufacturing method of sealed lead-acid battery
JP2809634B2 (en) Manufacturing method of sealed lead-acid battery
JPH0530291Y2 (en)
JP3951285B2 (en) Control valve type lead acid battery
JP3114419B2 (en) Sealed storage battery
Shi et al. Effect of perfluoroalkylsulfonate on the discharge behaviour of PbO2 electrodes in sulfuric acid solution
JPS60207262A (en) Sealed lead storage battery
JPH01149376A (en) Sealed lead-acid battery
JPS61502714A (en) Sealed lead-acid battery for oxygen gas recombination
JPH0628782Y2 (en) Sealed lead acid battery
JPS6327827B2 (en)
Bagshaw Materials in the design of recombination lead-acid cells
JPH0352189B2 (en)
JPS62281270A (en) Lead storage battery