JPH01195674A - Manufacture of lead-acid battery - Google Patents

Manufacture of lead-acid battery

Info

Publication number
JPH01195674A
JPH01195674A JP63019184A JP1918488A JPH01195674A JP H01195674 A JPH01195674 A JP H01195674A JP 63019184 A JP63019184 A JP 63019184A JP 1918488 A JP1918488 A JP 1918488A JP H01195674 A JPH01195674 A JP H01195674A
Authority
JP
Japan
Prior art keywords
active material
electrode plate
current collector
plate
paste
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
JP63019184A
Other languages
Japanese (ja)
Other versions
JPH0520873B2 (en
Inventor
Tadashi Yoneda
米田 忠司
Toshiyuki Matsumura
敏之 松村
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 JP63019184A priority Critical patent/JPH01195674A/en
Publication of JPH01195674A publication Critical patent/JPH01195674A/en
Publication of JPH0520873B2 publication Critical patent/JPH0520873B2/ja
Granted 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
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/06Lead-acid accumulators
    • H01M10/12Construction or manufacture
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/489Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties
    • 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 extend the life by filling paste in a current collector, bringing an active material protector into contact with it, drying them under compression as they are, electrode plates are stacked via a pressure transferring plate, forming an electrode plate group, and storing it in a battery jar in the compressed state. CONSTITUTION:An active material protector 3 is brought into contact with a positive electrode plate filled with an active material kneaded with lead powder and dilute sulfuric acid on a current collector 1, a pressure transferring plate 4 is brought into contact via the active material protector 3 and pressed, the active material is closely stuck to the surface of the electrode plate and dried. A separator 5 and a negative electrode plate 6 are stacked, an electrode plate group is stored in a battery jar in the compressed state. The generation and growth of basic lead sulfate crystals occur in paste by the drying under compression after the paste is filled, the strength of the current collector 1 is increased by a dried paste layer 2, and the deformation during the subsequent electrode plate processing process is prevented. The stress of the active material layer 2 is absorbed by the closely stuck active material protector 3 while a battery is in use. The deformation (waving, warping) of the electrode plate in the thickness direction is prevented by the pressure transferring plate 4.

Description

【発明の詳細な説明】 産業上の利用分野 本発明はメンテナンスフリー機能をもったペースト式鉛
蓄電池の寿命特性改善に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to improving the life characteristics of a paste type lead-acid battery having a maintenance-free function.

従来の技術 メンテナンスフリー化のために従来よりP b −Ca
  Sh系鉛合金集電体が広く用いられている。
Conventional technologyIn order to make maintenance free, P b -Ca
Sh-based lead alloy current collectors are widely used.

この合金系においてはCa含有率を高めて集電体の強度
をあげハンドリング性を確保している。
In this alloy system, the Ca content is increased to increase the strength of the current collector and ensure handling properties.

発明が解決しようとする課題 集電体の合金組成中のCaは強度を高める効果があるが
、充放電に伴う集電体の腐食によって集電体が伸びなど
の変形が生じ、陽極板全体が伸びたり、変形することは
防止できない。一方Sbは集電体の強度を高める作用は
特にないが、合金自体の耐食性を向上させ、集電体の腐
食に伴う伸びや変形を抑制し陽極板自体の変形を防止す
る効果がある。すなわち 集電体の合金組成中のCaとshの含有量は、Caは少
ない程、またshは多い程陽極板の耐久性向上に良い。
Problems to be Solved by the Invention Ca in the alloy composition of the current collector has the effect of increasing strength, but corrosion of the current collector during charging and discharging causes deformation such as elongation of the current collector, causing the entire anode plate to deteriorate. It cannot be prevented from stretching or deforming. On the other hand, Sb does not particularly have the effect of increasing the strength of the current collector, but has the effect of improving the corrosion resistance of the alloy itself, suppressing elongation and deformation accompanying corrosion of the current collector, and preventing deformation of the anode plate itself. That is, regarding the content of Ca and sh in the alloy composition of the current collector, the lower the content of Ca and the higher the content of sh, the better the durability of the anode plate will be improved.

しかしこの場合集電体強度は極度に低下し生産過程や電
池として使用中において早期に変形する。
However, in this case, the current collector strength is extremely reduced and deforms early during the production process or during use as a battery.

使用中の陽極板の変形を生じさせるものは、極板に対す
る加圧の不均一性や、充放電による活物質の組成変化に
伴って生じる応力および集電体の腐食による伸びである
Deformation of the anode plate during use is caused by uneven pressure applied to the plate, stress caused by changes in the composition of the active material due to charging and discharging, and elongation due to corrosion of the current collector.

本発明は極板に対する加圧の均一化を促進するとともに
前記性の2要因の影響を低減し陰極板の変形発生時期を
遅延ならしめるものである。
The present invention promotes uniformity of pressure applied to the electrode plate, reduces the effects of the above two factors, and delays the occurrence of deformation of the cathode plate.

3題を解決するための手段 集電体にペーストを充填した後、活物質保護体を当接し
そのまま加圧下で乾燥させることによって、電池に組み
込まれる迄の変形を防止する。この防止を可能とするの
は乾燥したペースト層である。
Means for Solving the Three Problems After filling the current collector with paste, the active material protector is brought into contact with the current collector and dried under pressure to prevent deformation before it is assembled into a battery. It is the dry paste layer that makes it possible to prevent this.

極板を加圧伝達板を介して重ね合わせ掻板群を作成し加
圧状態で電槽に収納することにより極板の変形(波打ち
、くびれ、そり)を抑制する。
Deformation (waving, constriction, warpage) of the electrode plates is suppressed by overlapping the electrode plates via a pressure transmission plate to create a group of scraped plates and storing them in a battery case under pressure.

作用 ペースト充填後の加圧下における乾燥により、塩基性硫
酸鉛結晶の生成、成長がペースト中に生じ集電体は乾燥
ペースト層によって強度が増加し、その後の極板加工工
程中の変形が防止される。
Effect Drying under pressure after filling the paste causes the formation and growth of basic lead sulfate crystals in the paste, and the strength of the current collector is increased by the dry paste layer, preventing deformation during the subsequent plate processing process. Ru.

電池使用中においては、活物質層の応力は密着した活物
質保護体によって吸収される。
During use of the battery, stress in the active material layer is absorbed by the active material protector in close contact with the active material layer.

加圧伝達板によって極板の厚み方向への変形(波打ち、
そり)が防止される。
The pressure transmission plate deforms the electrode plate in the thickness direction (waving,
Warping) is prevented.

実施例 本発明の一実施例を以下に示す。Example An example of the present invention is shown below.

集電体1のpb基以外合金組成はCa含有回がo、 0
5 wL%、Sh含有ff12.5wt%のもので強度
は極めて弱い。充填ペースト2は硫酸鉛を] 6wt%
含むものを陽極に、13wt%含むものを陰鳳に用いた
The alloy composition other than the PB base of the current collector 1 has a Ca content of o, 0.
5 wL%, Sh content ff12.5 wt%, and the strength is extremely weak. Filling paste 2 contains lead sulfate] 6wt%
The one containing 13 wt% was used for the anode, and the one containing 13 wt% was used for the inho.

活物質保護体3として若干のバインダーを含ム平均径1
0μmの含アルカリガラス細繊維からなる厚さ15鴫不
織布を用いた。加圧伝達板4として厚み1.0 mのポ
リエチレン成型体を更に加工したものを用いた。セパレ
ータ5は通常用いられる市販用電池の串状合成繊維セパ
レータ(厚み05馴)を用いた。
Contains some binder as active material protector 3 Average diameter 1
A 15-thick nonwoven fabric made of alkali-containing glass fine fibers of 0 μm was used. As the pressure transmission plate 4, a polyethylene molded body having a thickness of 1.0 m and further processed was used. As the separator 5, a skewer-shaped synthetic fiber separator (thickness: 05 mm) of a commonly used commercially available battery was used.

これらの部材を次の順序で組み立て性能評価用電池とし
た。
These members were assembled in the following order to form a battery for performance evaluation.

陽極の集電体にペーストを平滑に6υ/枚充填し、活物
質保護体を両面より当接したのち更に加圧伝達板を両面
より当接する。この状態で加圧伝達板に加圧(30Kq
/ d m’)を加え極板をきょう正する。加圧を加え
た状態で120℃の空気中に5分間入れペーストを乾固
させる。その後セパレータと陰極板6を重ねて当接し極
板群とする。この極板群にl Q K9/ dm’の群
加圧を与えた状態で電槽に収納する。
The current collector of the anode is smoothly filled with 6υ/sheet of paste, and the active material protector is brought into contact with it from both sides, and then the pressure transmission plate is brought into contact with it from both sides. In this state, apply pressure to the pressure transmission plate (30Kq
/ d m') to correct the electrode plate. The paste is dried by placing it in air at 120°C for 5 minutes under pressure. Thereafter, the separator and cathode plate 6 are overlapped and brought into contact to form an electrode plate group. This electrode plate group is stored in a battery case with a group pressure of l Q K9/dm' applied thereto.

従来品は以下要領で作成した。The conventional product was created as follows.

集電体1およびペースト2は前述の本発明品と同じもの
を用い、ペースト充填(60p/枚)後乾燥したのち活
物質保護体く厚み1.8mm)3、セパレータ5および
陰極板6を重ねて極板群を作成した。この極板群に30
Kv/dm2の加圧を与えた状態で電槽に収納した。
The current collector 1 and paste 2 were the same as those of the above-mentioned product of the present invention, and after filling the paste (60p/sheet) and drying, the active material protector (thickness: 1.8 mm) 3, separator 5, and cathode plate 6 were stacked. A group of electrode plates was created. 30 in this electrode group
It was stored in a battery case while being pressurized at Kv/dm2.

これまで述べた要領で電池(従来品、本発明品)を作成
し、電槽化成して寿命評価用の試料電池とした。試料電
池の概要を第1表に示した。
Batteries (conventional products and products of the present invention) were produced in the manner described above, and subjected to battery cell formation to provide sample batteries for life evaluation. An overview of the sample battery is shown in Table 1.

第  1  表 寿命評価の試験条件を第2表に示した。Table 1 Test conditions for life evaluation are shown in Table 2.

第  2  表 以下図面について説明する。Table 2 The drawings will be explained below.

第1図はペーストを充填したあとの本発明と従来の製造
工程を略記したものである。本発明は乾燥(従来1.O
WL%以下の水分にする)工程の前に活物質保護体と加
圧伝達板を当接し、その後に乾燥工程に移ることが従来
と大きく違うところである。
FIG. 1 schematically shows the manufacturing process of the present invention and the conventional method after filling with paste. The present invention is suitable for drying (conventional 1.O
The major difference from the conventional method is that the active material protector and the pressure transmission plate are brought into contact with each other before the process (to reduce the moisture content to below WL%), and then the drying process is started.

第2図は本発明における陽極板に活物質保護体と加圧伝
達板を当接した状態を正面より示したものである。また
第3図は更にセパレータと陰極板を当接した状態の断面
を示したもので本発明の特徴となる断面をA−A’と記
しである。同様に従来のものについて第4図および第5
図に示した。
FIG. 2 is a front view showing the state in which the active material protector and the pressure transmitting plate are in contact with the anode plate according to the present invention. Further, FIG. 3 further shows a cross section of the separator and the cathode plate in contact with each other, and the cross section which is a feature of the present invention is indicated by AA'. Similarly, Fig. 4 and 5 for the conventional one.
Shown in the figure.

第6図は寿命試験の結果を示したものである。FIG. 6 shows the results of the life test.

寿命となるサイクル数は、本発明品は約1400サイク
ルであるのに対し従来品は約1000サイクルであった
。4096程度の向上が認められる。
The life span of the product of the present invention was approximately 1,400 cycles, while that of the conventional product was approximately 1,000 cycles. An improvement of about 4096 is recognized.

また本発明品はサイクル数600から1000の間に比
較的安定な電圧性能を示すことが認められた。このサイ
クル数付近は活物質が微細化しはじめるとともに、陽極
集電体の腐食が表層を経て内部を進行していく時期であ
り、本発明品はそのような陽極板の劣化による放電電圧
の低下現象を抑制している。
It was also confirmed that the product of the present invention exhibited relatively stable voltage performance between 600 and 1000 cycles. Around this number of cycles, the active material begins to become finer and the corrosion of the anode current collector progresses through the surface layer and inside.The product of the present invention is designed to reduce the discharge voltage drop caused by such deterioration of the anode plate. is suppressed.

なお電池個数は本発明、従来品共3個である。Note that the number of batteries is three for both the present invention and the conventional product.

発明の効果 本発明による製造方法によれば比較的集電体の強度の弱
い合金組成を用いることが可能となり寿命性能に大きく
効果を発揮する。
Effects of the Invention According to the manufacturing method according to the present invention, it is possible to use an alloy composition with relatively low strength for the current collector, which greatly improves life performance.

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

第1図は本発明と従来の製造工程説明図、第2図は本発
明の陽極板正面図、 第3図は本発明の陽極板を用いた極板群の断面図、第4
図は従来の陽極板正面図、 第5図は従来の陽極板を用いた極板群の断面図、第6図
は寿命評価の結果特性図である 1: 集電体 2: ペースト層 3: 活物質保護体 4: 加圧伝達板 5: セパレータ 6: 陰極板
Fig. 1 is an explanatory diagram of the manufacturing process of the present invention and the conventional manufacturing process, Fig. 2 is a front view of the anode plate of the present invention, Fig. 3 is a cross-sectional view of an electrode plate group using the anode plate of the present invention, and Fig. 4
The figure is a front view of a conventional anode plate, Figure 5 is a cross-sectional view of an electrode plate group using a conventional anode plate, and Figure 6 is a characteristic diagram of the results of life evaluation. 1: Current collector 2: Paste layer 3: Active material protector 4: Pressure transmission plate 5: Separator 6: Cathode plate

Claims (1)

【特許請求の範囲】[Claims] 鉛または鉛合金からなる集電体に鉛粉と希硫酸を練合し
た活物質を充填した陽極板に活物質保護体を当接し更に
活物質保護体を介して加圧伝達板を当接して押圧し活物
質体を極板表面に密着(圧接)させた状態で乾燥させ、
その後セパレータおよび陰極板を重ねて再び加圧状態で
極板群を電槽に収納することを特徴とする鉛蓄電池製造
法。
An active material protector is brought into contact with an anode plate filled with an active material made by mixing lead powder and dilute sulfuric acid into a current collector made of lead or lead alloy, and a pressure transmission plate is further brought into contact through the active material protector. Press and dry the active material body in close contact (pressure contact) with the electrode plate surface,
A lead-acid battery manufacturing method characterized by stacking a separator and a cathode plate and storing the electrode plate group in a battery case again under pressure.
JP63019184A 1988-01-29 1988-01-29 Manufacture of lead-acid battery Granted JPH01195674A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63019184A JPH01195674A (en) 1988-01-29 1988-01-29 Manufacture of lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63019184A JPH01195674A (en) 1988-01-29 1988-01-29 Manufacture of lead-acid battery

Publications (2)

Publication Number Publication Date
JPH01195674A true JPH01195674A (en) 1989-08-07
JPH0520873B2 JPH0520873B2 (en) 1993-03-22

Family

ID=11992252

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63019184A Granted JPH01195674A (en) 1988-01-29 1988-01-29 Manufacture of lead-acid battery

Country Status (1)

Country Link
JP (1) JPH01195674A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100402967B1 (en) * 1998-12-18 2003-12-18 에스케이씨 주식회사 Slim lithium ion polymer battery manufacturing method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100402967B1 (en) * 1998-12-18 2003-12-18 에스케이씨 주식회사 Slim lithium ion polymer battery manufacturing method

Also Published As

Publication number Publication date
JPH0520873B2 (en) 1993-03-22

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