JPH02262253A - Lead-acid battery - Google Patents
Lead-acid batteryInfo
- Publication number
- JPH02262253A JPH02262253A JP1083474A JP8347489A JPH02262253A JP H02262253 A JPH02262253 A JP H02262253A JP 1083474 A JP1083474 A JP 1083474A JP 8347489 A JP8347489 A JP 8347489A JP H02262253 A JPH02262253 A JP H02262253A
- Authority
- JP
- Japan
- Prior art keywords
- lead
- cathode
- acid battery
- battery
- tellurium
- 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
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
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/68—Selection of materials for use in lead-acid accumulators
- H01M4/685—Lead alloys
-
- 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)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Connection Of Batteries Or Terminals (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、充電時に陽極から発生する酸素ガスを陰極で
吸収する、いわゆる陰極吸収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 so-called cathode absorption type lead-acid battery, in which the cathode absorbs oxygen gas generated from the anode during charging.
従来の技術
陰極吸収式の鉛蓄電池は、充電時あるいは自己放電時に
陽極から発生ずる酸素ガスを陰極活物質である金属鉛に
吸収させ、ガス発生による電池内圧の上昇を防止すると
としに、電解液の減少を抑える機能を有している。この
機能を達成するため格子体、極板群接合部及び極柱の合
金を選定するにあたって、
水素過電圧が高く、電池を充電した時酸素を発生しにく
く、
添加した元素が陰極に移動して自己放電を起こすことが
ない、
ということを考虜して、合金組成を決めている。Conventional technology In cathode absorption type lead-acid batteries, metal lead, which is the cathode active material, absorbs oxygen gas generated from the anode during charging or self-discharge, and an electrolytic solution is used to prevent the internal pressure of the battery from increasing due to gas generation. It has the function of suppressing the decrease in In order to achieve this function, we selected alloys for the lattice, plate group joints, and pole pillars because they have a high hydrogen overvoltage and are difficult to generate oxygen when the battery is charged. The alloy composition was determined with the consideration that it would not cause electrical discharge.
このように陰極吸収式鉛蓄電池は使用時に電解液の減少
が少ないため、面倒な加水作業が不要となり、蓄電池を
密閉化できるようになった。さらに密閉化することによ
り、使用中に有害なガスを蓄電池外に排出するこ古がな
くなり、室内においても手軽に蓄電池を使用できるよう
になった。In this way, cathode absorption type lead-acid batteries have less loss of electrolyte during use, so the troublesome work of adding water is no longer necessary, and the storage battery can now be sealed. Furthermore, by sealing the battery, there is no need to emit harmful gases outside the battery during use, and the battery can now be easily used indoors.
発明が解決しようとする課題
しかしなから、従来の陰極吸収式鉛蓄電池を使用中、特
にスタンバイ使用など常時充電されているような使用状
況の中で、陰極極柱、陰極格子体、陰極格子耳部、ある
いは陰極極板群接合部において急激な腐食が進行し、上
記部材の一部が破断する現象があった。陰極吸収式鉛蓄
電池内は、使用時においては常に陽極から発生する酸素
ガスが充満した状態にある。Problems to be Solved by the Invention However, when using a conventional cathode absorption type lead-acid battery, especially in situations where it is constantly being charged such as in standby use, the cathode pole, cathode grid body, and cathode grid ear There was a phenomenon in which rapid corrosion progressed at the joints of the cathode plates or the joints of the cathode plates, causing some of the members to break. During use, a cathode absorption lead-acid battery is always filled with oxygen gas generated from the anode.
従って酸素ガスを吸収する機能をもたせた陰極活物質は
もちろん、陰極格子体、極板群接合部及び極柱も常に酸
素に暴露されており、このために陰極部材の腐食、破断
が起こるものと想定される。この想定に基づき、種々検
討か行われてきたがはっきりとした原因を特定するには
至っていなかった。Therefore, not only the cathode active material, which has the function of absorbing oxygen gas, but also the cathode grid, electrode plate group joints, and pole columns are constantly exposed to oxygen, which can lead to corrosion and breakage of the cathode members. is assumed. Based on this assumption, various studies have been conducted, but no clear cause has been identified.
この従来の陰極吸収式鉛蓄電池で、スタンバイ使用中に
陰極部材の腐食が進行し、部材の破断に至った蓄電池を
詳細に解析したところ、腐食を受けた箇所1部分におい
ては腐食を受けなかった箇所に比べて、意図して添加し
てはいないテルルが多(含まれていることがわかった。A detailed analysis of this conventional cathode absorption lead-acid battery in which corrosion of the cathode material progressed during standby use, leading to the material breaking, revealed that the one area that had been corroded was not corroded. It was found that there was a large amount of tellurium (which was not intentionally added) compared to other parts.
さらに、テルルの量がふえるに従い腐食量は加速的にふ
え、従来は微量として特に影響がないとされてきたテル
ルの量を管理することが、陰極部材の腐食を防止するた
めに重要であることがわかった。Furthermore, as the amount of tellurium increases, the amount of corrosion increases at an accelerated pace, and it is important to control the amount of tellurium, which was previously considered to be a very small amount with no particular effect, in order to prevent corrosion of cathode members. I understand.
課題を解決するための手段
そこで本発明は、陰極吸収式を適用した鉛蓄電池におい
て、極板耳部を含む陰極格子体、極板群接合部及び極柱
のいずれか、あるいはこれらの全てがテルル含有量を2
01)9m以下とした鉛あるいは鉛合金から構成したも
のである。Means for Solving the Problems Therefore, the present invention provides a lead-acid battery to which a cathode absorption type is applied, in which either or all of the cathode grid body including the electrode plate ears, the electrode plate group joints, and the pole columns are made of tellurium. content 2
01) It is made of lead or lead alloy and has a length of 9 m or less.
作用
陰極格子体、極板群接合部及び極柱を構成する鉛あるい
は鉛合金中に不純物として含まれるテルル量を20pp
lIl以下に抑えることにより、陰極吸収式鉛蓄電池使
用中の過酷な酸素雰囲気にあっても、陰極部材は腐食を
受けにくく破断に至ることはない。従って陰極吸収式鉛
蓄電池の信頼性を著しく向とすることができる。The amount of tellurium contained as an impurity in the lead or lead alloy constituting the working cathode grid, electrode plate group joints, and pole columns is reduced to 20pp.
By keeping it below lIl, the cathode member is less susceptible to corrosion and will not break even in the harsh oxygen atmosphere during use of the cathode absorption lead-acid battery. Therefore, the reliability of the cathode absorption type lead-acid battery can be significantly improved.
実施例 以下、本発明の詳細な説明する。Example The present invention will be explained in detail below.
負極吸収式鉛蓄電池の構成を第1図に示す。図中1は負
極極板群接合部、2は負極格子体、3は極板耳部、4は
負極極柱、5は正極板、6はU字状セパレータである。Figure 1 shows the configuration of a negative electrode absorption lead-acid battery. In the figure, 1 is a negative electrode plate group joint, 2 is a negative electrode grid, 3 is an electrode tab, 4 is a negative pole, 5 is a positive electrode plate, and 6 is a U-shaped separator.
本発明の効果を明らかにするため、陰極極板群接合部1
に含まれるテルルの量を150ppm、 50pp+n
。In order to clarify the effects of the present invention, the cathode plate group joint 1
The amount of tellurium contained in is 150ppm, 50pp+n
.
30ppm、20ppm、 5ppmと変えて、この部
分が腐食によって破断するまでの時間を測定した。試験
には電圧12V、容量24Ahの陰極吸収式鉛蓄電池を
使用し13.8Vの定電圧充電を行いなから、1力月毎
に蓄電池容量及び内部抵抗の変化を測定した。なお、雰
囲気温度は40℃である。The concentration was changed to 30 ppm, 20 ppm, and 5 ppm, and the time until this part broke due to corrosion was measured. In the test, a cathode absorption lead-acid battery with a voltage of 12 V and a capacity of 24 Ah was used, and the battery was charged at a constant voltage of 13.8 V. Changes in battery capacity and internal resistance were measured every month. Note that the ambient temperature was 40°C.
上記の結果を第2図A、Bに示す。The above results are shown in FIGS. 2A and B.
第2図かられかるとおり、内部抵抗の急激な上昇が、テ
ルル量150ppu+では1力月で、50ppmでは3
力月で、30ppIIlでは6力月でそれぞれ起きてい
る。これらの蓄電池を分解して内部抵抗上昇の原因を調
べたところ、いずれも陰極極板群接合部の腐食による破
断てあった。As can be seen from Figure 2, the rapid rise in internal resistance occurred in 1 month at a tellurium content of 150 ppu+, and 3 months at a tellurium content of 50 ppu+.
It occurs in Rikizuki and 6 Rikizuki in 30ppIIl. When these batteries were disassembled to investigate the cause of the increase in internal resistance, it was discovered that all of the batteries had broken due to corrosion at the joints of the cathode plates.
しかしなから20ppm、 5pp+llでは18力月
を経過した段階でも急激な内部抵抗の上昇は見られない
。ただ容量は低下している。その原因を調べたところ、
いずれも陽極格子体の伸びによる短絡がその原因であり
、陰極極板群接合部には腐食破断は見られなかった。However, at 20 ppm and 5 pp+ll, no rapid increase in internal resistance was observed even after 18 months. However, capacity is decreasing. When we investigated the cause, we found that
In both cases, the cause was a short circuit due to elongation of the anode grid, and no corrosion fracture was observed at the joints of the cathode plate groups.
発明の効果
このように本発明による陰極吸収式鉛蓄電池は陰極格子
体、極板群接合部及び極柱を構成する鉛あるいは鉛合金
中に不純物として、20pplI+をこえるテルルを含
まないため、蓄電池イ・上用中に上記部材が腐食、破断
することがなく、また陰極吸収式鉛蓄電池にとって最も
重要な機能である電解液の減少、自己放電量も少なくで
きる。従って陰極吸収式鉛蓄電池の信頼性を著しく向上
させる効果がある。Effects of the Invention As described above, the cathode absorption type lead-acid battery according to the present invention does not contain tellurium in excess of 20 pplI+ as an impurity in the lead or lead alloy constituting the cathode grid, the electrode plate group joints, and the pole columns. - The above-mentioned members do not corrode or break during use, and the amount of electrolyte and self-discharge, which are the most important functions for cathode absorption lead-acid batteries, can be reduced. Therefore, it has the effect of significantly improving the reliability of the cathode absorption type lead-acid battery.
【図面の簡単な説明】
第1図は本発明の実施例による陰極吸収式鉛蓄電池の一
部断面図であり、第2図は本発明の効果を示すために行
った40℃雰囲気における連続充電試験の結果を示す図
である。
■・・・・・・極板群接合部、2・・・・・・陰極格子
体、3・・・・・・極板耳、4・・・・・・極柱、5・
・・・・・陽極板、6・・・・・・セパレータ。
代理人の氏名 弁理士 粟野重孝 ばか1名1− 膣硲
陽棲群砕番部
2− 績柘基1溪
3− 盪FJix杆
4− 階掻柘社
5−罎罹森
C−一で八′し−ダ[Brief Description of the Drawings] Fig. 1 is a partial cross-sectional view of a cathode absorption type lead-acid battery according to an embodiment of the present invention, and Fig. 2 shows continuous charging in a 40°C atmosphere to demonstrate the effects of the present invention. It is a figure showing the result of a test. ■... Plate group joint, 2... Cathode grid body, 3... Plate lug, 4... Pole column, 5...
... Anode plate, 6 ... Separator. Name of agent: Patent attorney Shigetaka Awano 1 idiot 1- vaginariyoseigunsaibanbu 2- 柘木 1 溪 3- ○FJix杆 4- 柘柘柘社 5-罎宎柘oriC-一で八' Shi-da
Claims (1)
いはこれらの全てが、テルル含有量20ppm以下の鉛
あるいは鉛合金から構成されていることを特徴とする鉛
蓄電池。A lead-acid battery characterized in that either or all of the cathode lattice, the electrode plate group joints, and the pole columns are made of lead or a lead alloy with a tellurium content of 20 ppm or less.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1083474A JPH02262253A (en) | 1989-03-31 | 1989-03-31 | Lead-acid battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1083474A JPH02262253A (en) | 1989-03-31 | 1989-03-31 | Lead-acid battery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH02262253A true JPH02262253A (en) | 1990-10-25 |
Family
ID=13803464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1083474A Pending JPH02262253A (en) | 1989-03-31 | 1989-03-31 | Lead-acid battery |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH02262253A (en) |
-
1989
- 1989-03-31 JP JP1083474A patent/JPH02262253A/en active Pending
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20080113268A1 (en) | Recombinant Hybrid Energy Storage Device | |
| JP2932491B2 (en) | Lead storage battery | |
| JPH0425676B2 (en) | ||
| JPH02262254A (en) | lead acid battery | |
| JPH02262251A (en) | lead acid battery | |
| JP2932490B2 (en) | Lead storage battery | |
| JPH02262256A (en) | lead acid battery | |
| JP2982170B2 (en) | Manufacturing method of cathode absorption type lead-acid battery | |
| JPH02262255A (en) | Lead-acid battery | |
| JPH02262250A (en) | Lead-acid battery | |
| JPS6264057A (en) | lead acid battery | |
| JP3185300B2 (en) | Sealed lead-acid battery | |
| JPH02262257A (en) | lead acid battery | |
| JPS5973849A (en) | non-aqueous electrolyte battery | |
| JP2953156B2 (en) | Stacked manganese dry battery | |
| JPS61153958A (en) | Maintenance-free lead acid battery | |
| JPS6048867B2 (en) | lead acid battery | |
| JPH02262249A (en) | lead acid battery | |
| JPH0418671B2 (en) | ||
| US3926677A (en) | Electric primary cells | |
| JPS6215767A (en) | organic electrolyte battery | |
| JPH0665032B2 (en) | Zinc alkaline battery | |
| JPS63226877A (en) | lead acid battery | |
| JPH02174072A (en) | lead acid battery | |
| JPS62208569A (en) | Sealed lead-acid battery |