JPS62200657A - Lead storage battery - Google Patents
Lead storage batteryInfo
- Publication number
- JPS62200657A JPS62200657A JP61042439A JP4243986A JPS62200657A JP S62200657 A JPS62200657 A JP S62200657A JP 61042439 A JP61042439 A JP 61042439A JP 4243986 A JP4243986 A JP 4243986A JP S62200657 A JPS62200657 A JP S62200657A
- Authority
- JP
- Japan
- Prior art keywords
- antimony
- lead
- alloy
- tin
- grid
- 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
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/06—Lead-acid accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/50—Current conducting connections for cells or batteries
- H01M50/528—Fixed electrical connections, i.e. not intended for disconnection
-
- 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)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Connection Of Batteries Or Terminals (AREA)
Abstract
Description
【発明の詳細な説明】 産業上の利用分野 本発明は鉛蓄電池の改良に関するものであり。[Detailed description of the invention] Industrial applications The present invention relates to improvements in lead-acid batteries.
使用中の電解液の減少を少なくできるメンテナンスフリ
ー電池を提供するものである。The present invention provides a maintenance-free battery that can reduce the loss of electrolyte during use.
従来の技術
鉛蓄電池用格子合金には、従来から、主とじでアンチモ
ン含有率が2〜5優の鉛合金か使用され、さらに、格子
鋳造性などの面から、各種の微量元素、たとえば、ヒ素
(As)、銅(Ou)などが添加されている。Conventional technology Lead alloys with an antimony content of 2 to 5 in the main seam have been used for grid alloys for lead-acid batteries, and in addition, from the viewpoint of grid castability, various trace elements, such as arsenic, have been used. (As), copper (Ou), etc. are added.
近年、自動利用、据置用など種々の用途に使イビし
用されている鉛蓄電池に無像−1lPlのニーズが高ま
り、それに伴なっ°C、アンチモン含有率が低い低アン
チモン合金を使用したり、アンチモンを全く含まないカ
ルシウム合金などを用いた電池が開発されCいる。さら
に、陽極と陰極の合金種類を異にした、いわゆる、ハイ
ブリッド構造を有する電池の開発も盛んである。In recent years, there has been an increase in the need for imageless -1lPl for lead-acid batteries, which are used for various purposes such as automatic and stationary use. Batteries using calcium alloys and the like that do not contain antimony have been developed. Furthermore, there is active development of batteries having a so-called hybrid structure in which the anode and cathode are made of different alloys.
この種のバッテリーは陽極に低アンチモン合金、陰極に
カルシウム合金を用いるなどし〔、電解液の族滅りに関
連する陰極の水素過電圧を下げないような工夫かされで
いる。This type of battery uses a low antimony alloy for the anode and a calcium alloy for the cathode, and is designed to avoid lowering the hydrogen overvoltage at the cathode, which is associated with electrolyte depletion.
しかしながら、この種の鉛蓄電池を製造する際には、複
数枚の陽、陰極板がストラップでそれぞれ並列に接続さ
れ、さらに、自動重用鉛蓄電池などのように12Vとす
るために、セル間接続部品を用い〔、単位電池が所定セ
ル数、直列に接続されるような構造を有し、両端のセル
には端子用のポールが設けられるような構造が基本であ
る。However, when manufacturing this type of lead-acid battery, multiple positive and negative electrode plates are connected in parallel with straps, and in order to achieve 12V as in automatic heavy-duty lead-acid batteries, intercell connection parts are required. [The basic structure is such that a predetermined number of unit batteries are connected in series, and the cells at both ends are provided with terminal poles.
従来からこの種の電池組立に用いられるや鉛合金にはコ
スト面などの点から一般的にアンチモン含有量の高い鉛
合金が多く用いられている。Conventionally, lead alloys with high antimony content have generally been used in this type of battery assembly from the viewpoint of cost.
そのため、製造時や使用時に、陽極酸化を受ける鉛合金
部ではsbイオンが溶出し易く、陰極還元を受ける部分
では水素発生が多くなり、各々が電池起雷力に影響を及
ぼし、使用中のみならず、放置中の自己放電性能も低下
させるという欠点を有していた。Therefore, during manufacturing and use, sb ions are easily eluted from the lead alloy part that undergoes anodization, and hydrogen generation increases in the part that undergoes cathodic reduction, each of which affects the battery's lightning power. First, it had the disadvantage that self-discharge performance during storage also deteriorated.
発明が解決しようとする問題点
本発明は、上記の点に鑑み、鉛蓄電池の液減り性能を改
良せんとするものである。Problems to be Solved by the Invention In view of the above-mentioned points, the present invention aims to improve the fluid reduction performance of lead-acid batteries.
問題点を解決するための手段
本発明は格子合金中のアンチモン含有率より大なるアン
チモン含有率から成る極板群ストラップ、ポール、セル
間接続体及び端子ポール、端子部の鉛合金に0.05〜
0.2重量パーセントのスズを含有せしめたものである
。Means for Solving the Problems The present invention provides a lead alloy for plate group straps, poles, intercell connectors, terminal poles, and terminal portions having an antimony content greater than that of the lattice alloy. ~
It contains 0.2% by weight of tin.
作用
上記特徴を有することにより、格子体より高アンチモン
を含有する鉛合金部品を製造する際、スズを微量添加す
ることによっ〔アンチモンが均一に分散分布し、また、
アンチモンとスズの金属間化合物(たとえば8 n@
S JSns Sb。Effect By having the above-mentioned characteristics, when manufacturing lead alloy parts containing higher antimony than the lattice body, by adding a small amount of tin, [antimony is distributed uniformly,
Intermetallic compounds of antimony and tin (e.g. 8 n@
S JSns Sb.
8ns Sb、など)が生成することなどによって、微
視的な合金状態の変化が考えられ、耐食性及びアンチモ
ンの陽極溶出の度合及び陰分極部での水素発生過電圧の
低下を抑制できるようになったものと考えられる。8ns Sb, etc.) is thought to cause a microscopic change in the state of the alloy, making it possible to suppress corrosion resistance, the degree of antimony elution from the anode, and the decrease in hydrogen generation overvoltage at the cathode polarization section. considered to be a thing.
この種の効果は据置用や自動東用船蓄電池に拘らず、酸
素過電圧や水素過電圧に起因するため、鉛−酸バッテリ
ー全般について効果を有する。This type of effect is caused by oxygen overvoltage and hydrogen overvoltage, and is effective for lead-acid batteries in general, regardless of whether they are stationary batteries or automatic marine storage batteries.
実施例 本発明の一実施例を説明する。Example An embodiment of the present invention will be described.
試験用鉛蓄電池とし〔、鋳造によってアンチモン含有量
が1.5.2.9.4.3重量パーセント(池の成分と
して、AsO,3重量パーセント、Sn0.05重量I
クーセント、80.03重量パーセント、残部鉛)の陽
極格子と、鋳造によってo、o8ffiJltパーセン
トカルシウム−〇。8重ffiバーセントスズからなる
陰極格子を用い、各格子体に常法に従って、所定の陽、
陰極ペーストを充填、乾燥しCW4板群を組立てた。そ
の際、第1表に示す如(、格子合金中のアンチモン含有
率を高くしたストラップ用合金(アンチモン3.0重量
パーセント)に、スズ含有量を調整した鉛#電池を製作
した。試験電池は5)−fR容b1が48Ahとし、初
充電後、電解液比重を1、280とした。As a test lead-acid battery, the antimony content was 1.5, 2, 9, 4.3% by weight by casting (the battery components were AsO, 3% by weight, Sn 0.05% by weight).
Cucent, 80.03 weight percent, balance lead) anode grid and cast by o, o8ffiJlt percent calcium-〇. A cathode lattice made of 8-fold ffi percent tin is used, and each lattice body is injected with predetermined positive and
The cathode paste was filled and dried to assemble the CW4 board group. At that time, as shown in Table 1, a lead-acid battery was fabricated using a strap alloy with a high antimony content in the lattice alloy (3.0 weight percent antimony) and an adjusted tin content.The test battery was 5) -fR capacity b1 was set to 48 Ah, and after initial charging, the electrolyte specific gravity was set to 1,280.
初充電後、電池を25°C水槽中でtSVの定電圧で連
続90日間試験を行って、電池重量減から減液量を求め
た後、陰極活物質に溶出した金属アンチモン量を原子吸
光法によって定量した。After the first charge, the battery was tested for 90 consecutive days at a constant voltage of tSV in a 25°C water tank, and the amount of liquid loss was determined from the battery weight loss.The amount of metallic antimony eluted into the cathode active material was measured using atomic absorption spectrometry. It was quantified by
@L表に試験電池の種類と液減り及び陰極活物質中のア
ンチモン量をまとめて示した。The @L table summarizes the types of test batteries, liquid loss, and amount of antimony in the cathode active material.
第1表
第1表から、陽極格子中のアンチモン含有率によっ〔、
液減り量は大きく変った。Table 1 From Table 1, depending on the antimony content in the anode lattice,
The amount of fluid lost has changed significantly.
■格子に1.5憾、2.7憾、4.3壬のアンチモン含
有位の鉛合金を用いた場合、スズが無添加あるいは0.
254以上添加の場合に比べ0.05〜0.21添加し
た場合の方が減液量は小さく、それを裏付けるように陰
極活物質への金属アンチモンへの析出量は小さいという
傾向かあり、本実施例によれば液減りが約【O〜20傷
抑制できる。0.1〜0.2重量パーセントを添加して
発明の効果
上述のように、本発明によれば鉛蓄電池の減液量が抑制
され、鉛蓄電池への補水頻度を少なくできるという効果
を有する。■When a lead alloy with an antimony content of 1.5 mm, 2.7 mm, or 4.3 mm is used for the grid, tin is not added or 0.5 mm.
The amount of liquid reduction is smaller when 0.05 to 0.21 is added than when 254 or more is added, and supporting this, there is a tendency that the amount of metal antimony deposited on the cathode active material is smaller. According to the embodiment, the liquid loss can be suppressed by approximately [0 to 20 scratches. Effects of the invention by adding 0.1 to 0.2 percent by weight As described above, the present invention has the effect of suppressing the amount of fluid loss in lead-acid batteries and reducing the frequency of water replenishment to lead-acid batteries.
Claims (1)
質的にアンチモンを含まない鉛又は鉛合金を用いた鉛蓄
電池において、陽極格子合金中のアンチモン含有率より
大なるアンチモン含有率から成る極板群ストラップ、ポ
ール及びセル間接続体及び端子ポール、端子の格子体外
の鉛合金中のスズ含有率が0.05〜0.2重量パーセ
ントとしたことを特徴とする鉛蓄電池。In a lead-acid battery using an antimony-based lead alloy for the anode grid alloy and a lead or lead alloy that does not substantially contain antimony for the cathode grid alloy, a group of electrode plates having an antimony content higher than the antimony content in the anode grid alloy. A lead-acid battery characterized in that the strap, the poles, the intercell connectors, the terminal poles, and the lead alloy outside the terminal grid have a tin content of 0.05 to 0.2 percent by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61042439A JPS62200657A (en) | 1986-02-27 | 1986-02-27 | Lead storage battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61042439A JPS62200657A (en) | 1986-02-27 | 1986-02-27 | Lead storage battery |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS62200657A true JPS62200657A (en) | 1987-09-04 |
Family
ID=12636103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61042439A Pending JPS62200657A (en) | 1986-02-27 | 1986-02-27 | Lead storage battery |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62200657A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01117269A (en) * | 1987-10-30 | 1989-05-10 | Shin Kobe Electric Mach Co Ltd | Group welding in lead-acid battery |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50112740A (en) * | 1973-11-23 | 1975-09-04 |
-
1986
- 1986-02-27 JP JP61042439A patent/JPS62200657A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS50112740A (en) * | 1973-11-23 | 1975-09-04 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01117269A (en) * | 1987-10-30 | 1989-05-10 | Shin Kobe Electric Mach Co Ltd | Group welding in lead-acid battery |
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