JPS61248359A - Manufacture of enclosed type lead storage battery - Google Patents

Manufacture of enclosed type lead storage battery

Info

Publication number
JPS61248359A
JPS61248359A JP60088252A JP8825285A JPS61248359A JP S61248359 A JPS61248359 A JP S61248359A JP 60088252 A JP60088252 A JP 60088252A JP 8825285 A JP8825285 A JP 8825285A JP S61248359 A JPS61248359 A JP S61248359A
Authority
JP
Japan
Prior art keywords
battery
electric current
positive
liquid
pbso4
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
JP60088252A
Other languages
Japanese (ja)
Inventor
Shinji Saito
慎治 斉藤
Asahiko Miura
三浦 朝比古
Takumi Hayakawa
早川 他く美
Satoshi Matsubayashi
敏 松林
Akio Komaki
小牧 昭夫
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.)
Resonac Corp
Original Assignee
Shin Kobe Electric Machinery 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 Shin Kobe Electric Machinery Co Ltd filed Critical Shin Kobe Electric Machinery Co Ltd
Priority to JP60088252A priority Critical patent/JPS61248359A/en
Publication of JPS61248359A publication Critical patent/JPS61248359A/en
Pending 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
    • H01M4/14Electrodes for lead-acid accumulators
    • H01M4/16Processes of manufacture
    • H01M4/22Forming of electrodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/06Lead-acid accumulators
    • H01M10/12Construction or manufacture
    • H01M10/128Processes for forming or storing electrodes in the battery container
    • 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

  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Secondary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To increase initial charge capacity for obtaining battery performance stably even if the battery is preserved for a long time at high-temperature condition by performing initial charge with electric current more than 0.025CA after supplying an amount of electrolytic solution into the battery excessively in comparison with the quantity of the liquid which can be well absorbed in a positive, a negative plates and a retainer, and thereafter, discharging the battery with low-electric current prior to initial charging process. CONSTITUTION:An amount of electrolytic solution excessive in comparison with the quantity of the liquid to be absorbed in a positive, a negative plate and a retainer, is supplied into a battery and the battery is discharged with low-electric current, so that much quantity of small crystallized PbSO4 is formed in the plate pores to retain sulfuric acid in the form of PbSO4. And further, the battery is charged with electric current more than 0.025CA, which is enough power to build up electric potential of the negative plate instead of high-electric current, to transform PbSO4 into PbO2 and at the same time, to retain much quantity of H2SO4 in the plate. PbO2 being produced during this period is formed in large crystal because the battery is charged with low-electric current, so that the porosity of the positive plate increases. And, since the battery is charged continuously until the free liquid is used up, the activity of the negative plate increases in parallel with gassing.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、陰、陽極板間にガラス繊維からなる不織布等
の隔離材(以下「リテーナ」という)に電解液を含浸、
保持させ、電池内を遊離液のない状態にした密閉型鉛電
池の製造法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is directed to impregnating an isolating material (hereinafter referred to as "retainer") such as a nonwoven fabric made of glass fiber with an electrolytic solution between negative and anode plates.
The present invention relates to a method for producing a sealed lead-acid battery in which the inside of the battery is free of free liquid.

従平の鈷缶 この種電池は、これまで輸出の場合や、長期保存される
場合の性能劣化等の対策が十分でなり)った。
Until now, there have been insufficient measures to prevent performance deterioration for this type of battery, such as when exporting or storing for a long period of time.

発明が解決しようとする問題点 この密閉型鉛電池は長期にわたってまた高温中で放置さ
れるお自己放電が促進され、極板の即用性能が損なわれ
て初期特性が劣る堝会があり、初充電を行っただけでは
、回復しない場曾がある。また高率放電用には特別の仕
様で極板から電池製作が必要である。
Problems to be Solved by the Invention When this sealed lead-acid battery is left in a high temperature for a long period of time, self-discharge is accelerated, the ready-to-use performance of the electrode plate is impaired, and the initial characteristics are poor. There are cases where the battery will not recover just by charging it. In addition, for high rate discharge, it is necessary to manufacture batteries from electrode plates with special specifications.

問題点を解決するための手段 本発明は上記問題点を除去下るもので、化成済の陰、陽
極板で電池を組立後、電池内へ電解液を注液する際、陽
、陰極板およびリテーナ中に吸液し得る液量に対して過
剰の電解液を注液した後、初充電工程の前に、小さな電
流で放電し、その後初光電を0.025CA以上の電流
を流して行ない、過剰の電解液馨分解させて遊離液のな
い状態にするものである。
Means for Solving the Problems The present invention eliminates the above-mentioned problems. After assembling a battery with chemically formed negative and anode plates, when injecting electrolyte into the battery, the positive and cathode plates and retainer are After injecting excess electrolyte with respect to the amount of liquid that can be absorbed into the tank, discharge with a small current before the initial charging process, and then perform the first photoelectric discharge with a current of 0.025 CA or more to remove excess electrolyte. The electrolyte solution is decomposed into a state in which there is no free liquid.

作用 初充電工程の前に、小さな電流で放電し、極板内に多量
の硫酸鉛を生成させて・光電すると・多量の硫酸を極板
内に保持し、陽極板の多孔度が増大し、し力1も、陰極
板の活性度が上することによって、初期容fを引き上げ
従来の電池容量lこ比べて高容量化することができる。
Before the initial charging process, a large amount of lead sulfate is generated in the electrode plate by discharging with a small current. When photoelectrically charged, a large amount of sulfuric acid is retained in the electrode plate, and the porosity of the anode plate increases. As the activation level of the cathode plate increases, the initial capacity f can be raised and the capacity can be increased compared to the conventional battery capacity l.

実施例 まず、電解液の注液量を陽・陰極板およびリテーナの吸
液量に対して過剰に注液する。ついで、小さな電流で放
電し、極板細孔内に小さな結晶のPI)304を多数生
成させて、硫酸yyr: pbso4の形で保持させる
ようにする。さらに、大電流でなく陰極板の電位が立上
る0、025 OA以上の電流で充電し、Pb30.を
Pbozに変換するとともに極板内に1−4≧S〜を多
く保持させるようにする。
Example First, the amount of electrolyte solution is injected in excess of the amount of liquid absorbed by the positive and cathode plates and the retainer. Then, by discharging with a small current, a large number of small crystals of PI) 304 are generated in the pores of the electrode plate and retained in the form of sulfuric acid yyr:pbso4. Furthermore, the Pb30. is converted into Pboz, and a large amount of 1-4≧S~ is retained in the electrode plate.

その際生成するpbo、は小さな電流で光電されるため
、大きな結晶となり、陽極板の多孔度は増大する。また
、光電量は、遊離液がなくなるまで充電するので、ガツ
シングお共に陰極板の活性度は増大する。
Since the pbo generated at this time is photoelectrically charged with a small current, it becomes large crystals and the porosity of the anode plate increases. Further, since the amount of photoelectric charge is charged until the free liquid is exhausted, the activity of the cathode plate increases with gassing.

本発明方法と従来方法(!:lこよる性能比較を第1表
と第2表に示す。第1表は極板の多孔度について従来方
法を1.0としたときのもので、また第2表は高率放電
時の電池の初期容量について同じ〈従来法を1.0とし
たときのものである。
Tables 1 and 2 show a performance comparison between the method of the present invention and the conventional method (! Table 2 shows the same initial capacity of the battery during high rate discharge (when the conventional method is set to 1.0).

第  1  表 第2表 第1表、第2表から明ら力)なように、本発明方法が従
来方法に比べて優れていることが判る。
It is clear from Tables 1 and 2 that the method of the present invention is superior to the conventional method.

発明の効果 以上のように、本発明は初充電全行うと極板内の■λS
σ斗量がまし、しかも多孔度が増大して、初期容量が増
大し、高温状態で長期保存しても電池性能が安定して得
られる等工業的価値大である。
Effects of the Invention As described above, the present invention reduces the
It has great industrial value, such as improved sigma weight, increased porosity, increased initial capacity, and stable battery performance even after long-term storage at high temperatures.

Claims (1)

【特許請求の範囲】[Claims] 陽・陰極板間にリテーナを当接させ電解液を保持させて
なる密閉型鉛電池の製造法において、電池組立後、電池
内へ電解液を注液する際、陽・陰極板およびリテーナ中
に吸液し得る液量に対して過剰の電解液を注液し、つい
で一度電池を小さい電流で放電した後、初充電を0.0
25CA以上の電流を流して行ない、過剰の電解液を分
解させて遊離液のない状態にすることを特徴とする密閉
型鉛電池の製造法。
In the manufacturing method of sealed lead-acid batteries, in which a retainer is placed in contact between the positive and negative electrode plates to hold the electrolyte, when pouring the electrolyte into the battery after battery assembly, the positive and negative electrode plates and the retainer are Inject an excess amount of electrolyte with respect to the amount of liquid that can be absorbed, then discharge the battery once with a small current, and then reduce the initial charge to 0.0.
A method for manufacturing a sealed lead-acid battery, which comprises passing a current of 25 CA or more to decompose excess electrolyte and make it free of free liquid.
JP60088252A 1985-04-24 1985-04-24 Manufacture of enclosed type lead storage battery Pending JPS61248359A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60088252A JPS61248359A (en) 1985-04-24 1985-04-24 Manufacture of enclosed type lead storage battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60088252A JPS61248359A (en) 1985-04-24 1985-04-24 Manufacture of enclosed type lead storage battery

Publications (1)

Publication Number Publication Date
JPS61248359A true JPS61248359A (en) 1986-11-05

Family

ID=13937671

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60088252A Pending JPS61248359A (en) 1985-04-24 1985-04-24 Manufacture of enclosed type lead storage battery

Country Status (1)

Country Link
JP (1) JPS61248359A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006093047A (en) * 2004-09-27 2006-04-06 Furukawa Battery Co Ltd:The Lead acid battery

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006093047A (en) * 2004-09-27 2006-04-06 Furukawa Battery Co Ltd:The Lead acid battery

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