JPS5861565A - Lead storage battery - Google Patents

Lead storage battery

Info

Publication number
JPS5861565A
JPS5861565A JP56159876A JP15987681A JPS5861565A JP S5861565 A JPS5861565 A JP S5861565A JP 56159876 A JP56159876 A JP 56159876A JP 15987681 A JP15987681 A JP 15987681A JP S5861565 A JPS5861565 A JP S5861565A
Authority
JP
Japan
Prior art keywords
alloy
performance
weight
lead
improved
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
JP56159876A
Other languages
Japanese (ja)
Inventor
Kunio Yonezu
米津 邦雄
Shigeharu Osumi
重治 大角
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.)
Japan Storage Battery Co Ltd
Nihon Denchi KK
Original Assignee
Japan Storage Battery Co Ltd
Nihon Denchi KK
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 Japan Storage Battery Co Ltd, Nihon Denchi KK filed Critical Japan Storage Battery Co Ltd
Priority to JP56159876A priority Critical patent/JPS5861565A/en
Publication of JPS5861565A publication Critical patent/JPS5861565A/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

Landscapes

  • Cell Electrode Carriers And Collectors (AREA)

Abstract

PURPOSE:To obtain a maintenance-free battery with the excellent initial performance and life performance by using an alloy lattice made of specific amounts of individual nucleus chemical agents such as antimony, tin, aluminum, arsenic, and sulfur and a remaining amount of lead. CONSTITUTION:A lead storage battery is formed using an alloy lattice made of nucleus chemical agents including 2% or less, by weight, of antimony, 0.1% or more, by weight, of tin, 0.001-0.1%, by weight, of aluminum, a proper amount of arsenic, and an infinitesimal amount of sulfur, or selenium, or copper and a remaining amount of lead. Accordingly, the hydrogen over voltage of a cathode plate is prevented from being dropped, requiring to supply no water, thus a maintenance-free battery can be obtained, and the stability of Sb of the Pb-Sb melted alloy is improved due to the coexistence with Al, the work performance is improved, the terminal voltage for rapid discharge is improved due to the adition of Sn furthermore, the crystallinity of the alloy is made extremely fine due to the addition of the nucleus chemical agents, thereby the initial performance and life performance can be improved.

Description

【発明の詳細な説明】 本発明は2i1t11%以下のアンチモン(8b)を含
む低アンチモン合金鋳造格子を用いた沿#電池に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a parallel battery using a low antimony alloy cast grid containing less than 2i1t11% antimony (8b).

負癒仮の水素過電子の低Fを防ぎ、抽水を不要とするメ
ンテナンス・フリー(MF)鉛**aが、格子に鉛(P
b)−カルシウム(Ca)系合金を用いることで商品化
されている。
Maintenance-free (MF) lead**a prevents low F of temporary hydrogen superelectrons and eliminates the need for water extraction.
b) - It has been commercialized by using a calcium (Ca) based alloy.

Pb−G*  格子は鋳造作業性が悪く、これを用いt
こj9#電池は深い充放電サイクルで短寿命である。池
万、8bの腫を2@置%以下のように少なくして、サイ
クル寿命の優れたMF 鉛蓄電池を開発する試みもある
。しかし2tii%以゛ドの低8b 合金では、溶湯の
sb の酸化速度が大きく安定し1こ組成の格子が得ら
れないばかりでなく、深い充放電サイクルで性能にバラ
ツキが大きく、短寿命の電池が多いという欠点があった
。とくに間−なのは急放電特性で、′1trJh仮の電
位が異′帛に低くてパワーが取り出せないことが多かつ
1こ。
Pb-G* lattice has poor casting workability, so using this
This j9# battery has a deep charge/discharge cycle and a short lifespan. There is also an attempt to develop a MF lead-acid battery with an excellent cycle life by reducing the number of 8b to 2% or less. However, in the case of low 8b alloys with a content of 2tii% or more, the oxidation rate of sb in the molten metal is high and stable, and not only is it impossible to obtain a lattice with a 1-component composition, but also the performance varies greatly during deep charge/discharge cycles, resulting in a short battery life. The disadvantage was that there were many Particularly problematic is the sudden discharge characteristic, where the temporary potential is so low that it is often impossible to extract power.

本発明は、低8b合金格子にかかわる上記の欠点を解消
し、初期性能および寿命性能が優れているMF沿J電池
を得ることを目的とするも重置%、ひ累適当處、いおう
(8)ま1こはセレン(8e)または銅(CI)などの
微處の核化剤、残部Pbからなる合金格子を用いること
にある。
The present invention aims to eliminate the above-mentioned drawbacks related to the low 8b alloy lattice and obtain a MF battery with excellent initial performance and lifetime performance. ) The first advantage is to use an alloy lattice consisting of a small amount of a nucleating agent such as selenium (8e) or copper (CI), and the balance being Pb.

禰々な組成の低sb 合金で格子の鋳造実験を行ない、
つぎにこの格子を用いて自動車用船蓄電−を試作し、初
期性能および寿命性能を調べた。1池は20時間率容量
が85アンペ・”・・アク−(AhJ7急放電の条件は
一15℃、150A放電とし、サイクル寿命試験は20
ムxth放電、5ムx5h充電で巧なった。なお鋳造実
験では約6時間鋳造してこの闇に8bがどれだけ減少す
るかを調べた。
We conducted a lattice casting experiment using a low sb alloy with a rich composition.
Next, we fabricated a prototype battery for automobiles using this grid, and examined its initial performance and lifetime performance. One cell has a 20-hour rate capacity of 85 amperes.
I got good at discharging for 1 hour and charging for 5 hours for 5 hours. In the casting experiment, the casting was carried out for about 6 hours to see how much 8b was reduced in this darkness.

第  1  表 実験結集は第1表に・ドした通りであり、Pb−8bは
  合金M場のSbは0.001W歇%以上のムl を
共存【  させろと安定性が良くなり、8n  の添加
も若干の、  効果が認められtこ。急放電の端子!干
およびサイクル寄合は8bが少ないと劣る傾向がみられ
ろが、8nをo、x重量%以上添加すると著しく改善さ
れ、中破のA1 も何効のようであつfコ。なおこの実
験ではP b−J b合金溶湯の凝固の核化剤としてS
を用いている。すなわち鋳造時に溶湯上に8のドロスを
浮かべ、浴−に飽和する電の8を俗解させている。
Table 1 The results of the experiments are as shown in Table 1. Pb-8b has better stability when Sb in the alloy M field coexists with a mulch of 0.001W or more. Some effects have also been observed. Sudden discharge terminal! Although drying and cycling tend to be inferior when 8b is small, it is significantly improved when 8n is added in an amount of o, x weight % or more, and it seems that even medium-broken A1 has some effect. In this experiment, S was used as a nucleating agent for the solidification of the Pb-Jb alloy molten metal.
is used. In other words, during casting, dross of 8 is floated on top of the molten metal, and the 8 of electricity saturates the bath.

低sb合金の鋳造ではこの核化剤の添加は重要であって
、 8 、 Se、 Cu Bgたはム1などのように
、解融Pb  を冷却しtこときに析出して初晶の核と
なるものを1%ili?1iのg*に飽和させておかな
いと、合金の結晶が粗大化し#4後結晶の粒界で破断し
°゛たり、電池内で粒界腐食を起こし早期に格子の崩壊
を生じる。
Addition of this nucleating agent is important in casting low sb alloys, and nucleating agents such as 8, Se, Cu, Bg, or Mu1 precipitate when the molten Pb is cooled and form primary crystal nuclei. What is 1%ili? If the alloy is not saturated to g* of 1i, the alloy crystals will become coarse and break at the grain boundaries of the #4 crystals, or intergranular corrosion will occur in the battery, resulting in early lattice collapse.

つぎに、最近採用されるようになった鉛合金シートをエ
キスバンド加工する方式の格子について、上記結果を確
認する実験を行なった。まずsblを変えたPb−8b
−8n−AI −As−8合金シー トラ製m L、、
エキスバンド加工したところ、8bが8重量%以上では
桟が切れたが、2電量%以下の場合には良好であつf:
、、このエキスバンド格子を用いて鋳造格子と同様に試
験した結果を@2表に示す。
Next, we conducted an experiment to confirm the above results regarding a grid of a method that expands lead alloy sheets, which has recently been adopted. First, Pb-8b with changed sbl
-8n-AI -As-8 alloy Sheetora M L,,
When extended band processing was performed, the crosspiece broke when 8b was 8% by weight or more, but it was good when the amount of electricity was 2% or less, and f:
,, The results of tests using this expanded grid in the same manner as the cast grid are shown in Table @2.

第  2  表 表から判るように、エキスバンド格子でもl(n  お
よびム1は急放電時の電圧特性やサイクル#命性能に効
果があり、鋳造格子と似た傾向を示している。
As can be seen from Table 2, even in the expanded grid, l(n and m1 have an effect on the voltage characteristics during rapid discharge and the cycle life performance, showing a similar tendency to that of the cast grid.

なおム1 は沿への溶解度が小さく、gas温度を高く
しても0.1重量%以上溶解させることは不可能であっ
た。
In addition, Mome 1 had a low solubility in the gas, and even if the gas temperature was raised, it was impossible to dissolve it in an amount of 0.1% by weight or more.

以上のように、本発明は鋳造が容易で初期および寿命性
能の優れtこメンテナンス・フリー鉛蓄電池を可能にし
たものである。
As described above, the present invention enables a maintenance-free lead-acid battery that is easy to cast and has excellent initial and life performance.

Claims (2)

【特許請求の範囲】[Claims] (1)  アンチモ、ン2ft%以下、才ず0.1蝋I
t%以上、アルミニウム0.001〜0.1電歇%、ひ
1g4当喰、いおうまたはセレンまたは銅などのamの
核化剤、残部給からなる合金格子を用いた沿II電池。
(1) Antimony 2 ft% or less, 0.1 wax I
A II battery using an alloy lattice consisting of t% or more, aluminum 0.001 to 0.1 electrification %, aluminum 1g4, sulfur, am nucleating agent such as selenium or copper, and the balance.
(2)  特許請求範囲第(1)項記載の沿1電韻にお
いて、格子をエキスバンド方式によってI+111aシ
fこもの。
(2) In the line 1 electronic rhyme described in claim (1), the lattice is expanded to I+111a by the expansion method.
JP56159876A 1981-10-07 1981-10-07 Lead storage battery Pending JPS5861565A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56159876A JPS5861565A (en) 1981-10-07 1981-10-07 Lead storage battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56159876A JPS5861565A (en) 1981-10-07 1981-10-07 Lead storage battery

Publications (1)

Publication Number Publication Date
JPS5861565A true JPS5861565A (en) 1983-04-12

Family

ID=15703128

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56159876A Pending JPS5861565A (en) 1981-10-07 1981-10-07 Lead storage battery

Country Status (1)

Country Link
JP (1) JPS5861565A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61135058A (en) * 1984-12-05 1986-06-23 Yuasa Battery Co Ltd Lead storage battery
JPS61224271A (en) * 1985-03-28 1986-10-04 Shin Kobe Electric Mach Co Ltd Lead storage battery
US5508125A (en) * 1994-03-21 1996-04-16 Globe-Union Inc. Battery straps made of a lead-based alloy containing antimony, arsenic, tin and selenium

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61135058A (en) * 1984-12-05 1986-06-23 Yuasa Battery Co Ltd Lead storage battery
JPH0367302B2 (en) * 1984-12-05 1991-10-22 Yuasa Battery Co Ltd
JPS61224271A (en) * 1985-03-28 1986-10-04 Shin Kobe Electric Mach Co Ltd Lead storage battery
US5508125A (en) * 1994-03-21 1996-04-16 Globe-Union Inc. Battery straps made of a lead-based alloy containing antimony, arsenic, tin and selenium

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