JPH01146254A - Seald lead-acid battery - Google Patents

Seald lead-acid battery

Info

Publication number
JPH01146254A
JPH01146254A JP62305005A JP30500587A JPH01146254A JP H01146254 A JPH01146254 A JP H01146254A JP 62305005 A JP62305005 A JP 62305005A JP 30500587 A JP30500587 A JP 30500587A JP H01146254 A JPH01146254 A JP H01146254A
Authority
JP
Japan
Prior art keywords
active material
grid
tin powder
acid battery
lattice
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.)
Granted
Application number
JP62305005A
Other languages
Japanese (ja)
Other versions
JP2553598B2 (en
Inventor
Keiko Naruse
成瀬 圭子
Hiroyuki Jinbo
裕行 神保
Toshihiro Inoue
利弘 井上
Yoshihisa Yagyu
柳生 芳久
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 JP62305005A priority Critical patent/JP2553598B2/en
Publication of JPH01146254A publication Critical patent/JPH01146254A/en
Application granted granted Critical
Publication of JP2553598B2 publication Critical patent/JP2553598B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/66Selection of materials
    • H01M4/68Selection of materials for use in lead-acid accumulators
    • H01M4/685Lead alloys
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/14Electrodes for lead-acid accumulators
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/56Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of lead
    • 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

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Cell Electrode Carriers And Collectors (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To prevent the formation of a passive layer and to lengthen the cycle life by adding 0.01-0.2wt.% tin powder to a positive active material. CONSTITUTION:0.01-0.2wt.% tin powder is added to a positive active material. It is preferable to use a Pb-Sn-As alloy in a positive grid and to add 0.01-0.2wt.% tin powder to the active material. The elongation of the grid of a sealed lead-acid battery and the formation of passive film on the interface between the grid and an active material are retarded, and the adhesion of the active material to the grid is increased. Capacity deterioration caused by constant microcurrent overcharge is retarded and the cycle life is lengthened.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はポータプル機器用として多方面に利用され、急
激に需要が増加している密閉型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 relates to sealed lead-acid batteries, which are used in a wide variety of applications for portable equipment, and whose demand is rapidly increasing.

従来の技術 密閉型鉛電池に関してはこれまでに数多くの提案がある
。代表的なものとして、電解液量を極板群の孔容積、も
しくはそれ以下にしてフリー液無しの状態とし、充電末
期に陽極板から発生する酸素ガスを陰極板に吸収させる
ことにより、電解液の減少を抑制する方式が採用されて
いる。この密閉型鉛蓄電池は横転や倒置しても漏液せず
、かつ補水不要であるという特徴を持っている。
Conventional Technology There have been many proposals regarding sealed lead-acid batteries. A typical example is to reduce the amount of electrolyte to the pore volume of the electrode plate group or less so that there is no free liquid, and to absorb the oxygen gas generated from the anode plate at the end of charging into the cathode plate. A method is adopted to suppress the decrease in This sealed lead-acid battery does not leak even if it is turned over or placed upside down, and it does not require water replenishment.

フ 発明が解決しよメとする問題点 上記従来の密閉型鉛蓄電池は、くり返し微少定電流過充
電を行った場合、容量劣化が起こり、サイクル寿命が低
下するという問題点を有していた。
Problems to be Solved by the Invention The above-mentioned conventional sealed lead-acid batteries had a problem in that when repeated slight constant current overcharging was performed, capacity deterioration occurred and cycle life was shortened.

この問題点の原因として、微少定電流過充電による格子
の伸び、および格子と活物質の界面に不働態層が形成さ
れることによる格子と活物質との界面の密着性の低下が
考えられる。
The causes of this problem are thought to be elongation of the lattice due to slight constant current overcharging and a decrease in adhesion between the lattice and the active material interface due to the formation of a passive layer at the interface between the lattice and the active material.

本発明は上記問題点を解決するもので、格子の伸びを抑
制し、格子と活物質との界面の密着性を向上させること
により、不働態層の形成を防ぎ、サイクル寿命を向上さ
せるものである。
The present invention solves the above problems by suppressing the elongation of the lattice and improving the adhesion of the interface between the lattice and the active material, thereby preventing the formation of a passive layer and improving the cycle life. be.

問題点を解決するだめの手段 前記の目的を達成するために、本発明の密閉型鉛蓄電池
はスズ粉末を陽極活物質中に重量比で0.01〜0.2
%添加した構成を有する。
Means for Solving the Problems In order to achieve the above object, the sealed lead-acid battery of the present invention contains tin powder in the anode active material in a weight ratio of 0.01 to 0.2.
% added.

好ましくは、陽極格子としてPb−5n−As合金(特
開昭54−87827号公報)を用い、かつスズ粉末を
0.01〜Q、2wt%添加した構成としたものである
Preferably, a Pb-5n-As alloy (Japanese Unexamined Patent Publication No. 54-87827) is used as the anode grid, and tin powder is added in an amount of 0.01 to Q, 2 wt%.

作用 この構成によって、密閉型鉛蓄電池の格子の伸び、およ
び格子と活物質との界面でおこる不働態層の形成を抑制
し、格子界面での密着性を向上させることによシ微少定
電流過充電による容量劣化を抑制し、サイクル寿命の向
上を実現することができる。
Effect: This structure suppresses the elongation of the lattice of a sealed lead-acid battery and the formation of a passive layer that occurs at the interface between the lattice and the active material, and improves the adhesion at the lattice interface, thereby suppressing slight constant current overload. Capacity deterioration due to charging can be suppressed and cycle life can be improved.

実施例 以下本発明の実施例について図を参照しながら説明する
EXAMPLES Examples of the present invention will be described below with reference to the drawings.

正極板としてPb−8n−As合金よりなる格子に、鉛
粉重量当たり0.005〜Q、3%のスズ粉末を練合時
に添加したペーストを充填し、極板を試作した。
A positive electrode plate was prepared by filling a lattice made of a Pb-8n-As alloy with a paste in which tin powder of 0.005 to 3% by weight of lead powder was added during kneading.

これらの正極板1枚および従来処方の負極板1枚、ガラ
スマット1枚を組み合わせ、電解液として比重1.34
(20°C)の希硫酸を用いて、電圧8v、容量1.1
人h (10時間率)の電池を試作した。なお本発明の
正極Aはスズを0.01%添加したもの、Bは同じく0
.1%、Cは同じ<0.2%添加したものである。
Combining one of these positive electrode plates, one conventionally formulated negative electrode plate, and one glass mat, the electrolyte has a specific gravity of 1.34.
(20°C) using dilute sulfuric acid, voltage 8V, capacity 1.1
A prototype battery with a 10-hour rate was manufactured. The positive electrode A of the present invention has 0.01% tin added, and the positive electrode B also has 0.01% tin added.
.. 1%, C with the same <0.2% addition.

第1図にこれらの電池A〜Cと、従来電池のサイクル寿
命特性を示す。
FIG. 1 shows the cycle life characteristics of these batteries A to C and a conventional battery.

なお、放電は12Ωの定抵抗を用いて放電電圧6.8v
までとし、充電は電流値440 mAの定電圧充電を6
時間おこなった。
In addition, the discharge voltage is 6.8V using a constant resistance of 12Ω.
Charging is performed using constant voltage charging with a current value of 440 mA for 600 mA.
It took time.

第2図のように、スズ粉末の添加量が0.01%未満の
場合は効果がなく、0.2%以上になると内部短絡が起
こり寿命特性が劣化する。
As shown in FIG. 2, if the amount of tin powder added is less than 0.01%, there is no effect, and if it is more than 0.2%, an internal short circuit occurs and the life characteristics deteriorate.

また、Snを含まない格子合金を用いた場合は効果がな
く、ムSは格子合金の機械的強度を向上させるため添加
した。
Further, when a lattice alloy containing no Sn was used, there was no effect, and S was added to improve the mechanical strength of the lattice alloy.

以上のように本実施例によれば、P b −8n−As
合金よりなる格子に鉛粉重量当たり0.01〜0.2%
のスズ粉末を添加したペーストを充填したことにより、
密閉型鉛蓄電池におけるサイクル寿命を大幅に向上させ
ることができる。
As described above, according to this embodiment, P b -8n-As
0.01 to 0.2% by weight of lead powder in a lattice made of alloy
By filling the paste with tin powder added,
The cycle life of sealed lead-acid batteries can be significantly improved.

発明の効果 本発明は、密閉型鉛蓄電池の正極活物質中にスズ粉末を
添加するとともに、正極格子としてPb−3n−As合
金を用いることにより、微少定電流過充電による格子の
伸び、および格子と活物質との界面でおこる不働態層の
形成を抑制し、格子界面での密着性を向上させて容量劣
化を抑制するものである。
Effects of the Invention The present invention adds tin powder to the positive electrode active material of a sealed lead-acid battery and uses a Pb-3n-As alloy as the positive electrode grid, thereby preventing the elongation of the grid due to slight constant current overcharging and This suppresses the formation of a passive layer at the interface between the active material and the active material, improves adhesion at the lattice interface, and suppresses capacity deterioration.

このような効果をもたらす原因は明らかではないが、正
極格子中のスズと陽極活物質中のスズの相互作用により
、格子と活物質との界面の密着性が向上したと推定され
る。このことにより、密閉型鉛蓄電池のサイクル寿命の
向上とともに高信頼性の密閉型鉛蓄電池の提供が可能と
なる。
Although the cause of this effect is not clear, it is presumed that the interaction between tin in the positive electrode lattice and tin in the positive electrode active material improves the adhesion at the interface between the lattice and the active material. This makes it possible to improve the cycle life of the sealed lead-acid battery and to provide a highly reliable sealed lead-acid battery.

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

第1図は本発明による試作電池と従来電池のサイクル寿
命を示す図、第2図はスズ粉末の添加量とサイクル寿命
の関係を示す図である。 本発明品人・・・・・・スズ粉末の添加量0.01wt
%、本発明品B・・・・スズ粉末の添加量0.1wt%
、本発明品C・・・・・・スズ粉末の添加量o、2wt
%。
FIG. 1 is a diagram showing the cycle life of a prototype battery according to the present invention and a conventional battery, and FIG. 2 is a diagram showing the relationship between the amount of tin powder added and the cycle life. Inventor: Added amount of tin powder: 0.01wt
%, Invention product B...Additional amount of tin powder 0.1wt%
, Invention product C...Additional amount of tin powder o, 2wt
%.

Claims (2)

【特許請求の範囲】[Claims] (1)スズ粉末を、重量比で0.01〜0.2%正極活
物質中に添加したことを特徴とする密閉型鉛蓄電池。
(1) A sealed lead-acid battery characterized in that 0.01 to 0.2% by weight of tin powder is added to a positive electrode active material.
(2)陽極格子としてPb−Sn−As合金を用いるこ
とを特徴とする特許請求の範囲第1項記載の密閉型鉛蓄
電池。
(2) The sealed lead-acid battery according to claim 1, wherein a Pb-Sn-As alloy is used as the anode grid.
JP62305005A 1987-12-01 1987-12-01 Sealed lead acid battery Expired - Lifetime JP2553598B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62305005A JP2553598B2 (en) 1987-12-01 1987-12-01 Sealed lead acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62305005A JP2553598B2 (en) 1987-12-01 1987-12-01 Sealed lead acid battery

Publications (2)

Publication Number Publication Date
JPH01146254A true JPH01146254A (en) 1989-06-08
JP2553598B2 JP2553598B2 (en) 1996-11-13

Family

ID=17939935

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62305005A Expired - Lifetime JP2553598B2 (en) 1987-12-01 1987-12-01 Sealed lead acid battery

Country Status (1)

Country Link
JP (1) JP2553598B2 (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53118742A (en) * 1977-03-25 1978-10-17 Japan Storage Battery Co Ltd Maintenance free type lead storage battery
JPS5487827A (en) * 1977-12-23 1979-07-12 Matsushita Electric Ind Co Ltd Grid for lead storage battery

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53118742A (en) * 1977-03-25 1978-10-17 Japan Storage Battery Co Ltd Maintenance free type lead storage battery
JPS5487827A (en) * 1977-12-23 1979-07-12 Matsushita Electric Ind Co Ltd Grid for lead storage battery

Also Published As

Publication number Publication date
JP2553598B2 (en) 1996-11-13

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