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JPS6054742B2 - Manufacturing method of electrode plates for lead-acid batteries - Google Patents
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JPS6054742B2 - Manufacturing method of electrode plates for lead-acid batteries - Google Patents

Manufacturing method of electrode plates for lead-acid batteries

Info

Publication number
JPS6054742B2
JPS6054742B2 JP55056485A JP5648580A JPS6054742B2 JP S6054742 B2 JPS6054742 B2 JP S6054742B2 JP 55056485 A JP55056485 A JP 55056485A JP 5648580 A JP5648580 A JP 5648580A JP S6054742 B2 JPS6054742 B2 JP S6054742B2
Authority
JP
Japan
Prior art keywords
lead
active material
electrode plates
acid batteries
electrode plate
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.)
Expired
Application number
JP55056485A
Other languages
Japanese (ja)
Other versions
JPS56152165A (en
Inventor
雅一 下田
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 JP55056485A priority Critical patent/JPS6054742B2/en
Publication of JPS56152165A publication Critical patent/JPS56152165A/en
Publication of JPS6054742B2 publication Critical patent/JPS6054742B2/en
Expired 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
    • H01M4/20Processes of manufacture of pasted electrodes
    • 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

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

Description

【発明の詳細な説明】 本発明は鉛蓄電池用極板の活物質中に添加されている合
成繊維に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to synthetic fibers added to the active material of electrode plates for lead-acid batteries.

従来、鉛蓄電池用極板の活物質中には、極板の製造工程
あるいは鉛蓄電池の組立工程または鉛蓄電池の使用中に
おける活物質の脱落を防止するために、太さ2乃至5デ
ニール、長さ0.5乃至3ミリ程度の耐酸性を有する例
えばアクリルと塩化ビニールの共重合体からなる合成繊
維が混入されている。
Conventionally, the active material of the electrode plates for lead-acid batteries has a thickness of 2 to 5 denier and a length of 2 to 5 denier to prevent the active material from falling off during the electrode plate manufacturing process, the lead-acid battery assembly process, or the use of the lead-acid battery. For example, synthetic fibers made of a copolymer of acrylic and vinyl chloride, which have an acid resistance of about 0.5 to 3 mm, are mixed.

しカルながら、上記の如き合成繊維は表面が滑らかなた
め、活物質との密着性が悪く、活物質の脱落を防止する
という効果が十分であるとはいえない。
However, since the synthetic fibers described above have smooth surfaces, they have poor adhesion to the active material, and cannot be said to be sufficiently effective in preventing the active material from falling off.

合成繊維を添加することによる活物質の脱落を防止する
効果としては、合成繊維の添加量を増したり、長さを長
くすることによつてある程度期待することはできるが、
一方においては、格子基板へのペーストの充填剤が劣下
する等極板製造工程上の開発生の原因となる惧れがある
ために添加量を増したり、長さを長くするには限度があ
る。そこで最近においては合成繊維の断面形状を変形さ
せたり、繊維を波状に加工する等の工夫がなされている
が、効果は少なく、実用的でないものが多い。本発明は
上記の点に鑑み、添加する合成繊維中に活物質の原材料
に用いる鉛化合物の粉末を保持せしめることで、活物質
との密着性の向上を図り、活物質の脱落を少なくして、
極板製造工程や鉛蓄電池の組立工程における不良発生を
低減し、惹いては電池寿命を延長ならしめんとするもの
である。
Although the effect of adding synthetic fibers to prevent the active material from falling off can be expected to some extent by increasing the amount of synthetic fibers added or increasing the length,
On the other hand, there are limits to increasing the amount added or increasing the length because there is a risk of deterioration of the filler in the paste to the grid substrate, which may cause problems in the manufacturing process of the equipolar plate. be. Recently, attempts have been made to change the cross-sectional shape of synthetic fibers or process the fibers into waves, but these efforts have little effect and are often impractical. In view of the above points, the present invention aims to improve adhesion with the active material by retaining powder of a lead compound used as a raw material for the active material in the synthetic fibers added, thereby reducing the dropout of the active material. ,
The aim is to reduce the occurrence of defects in the electrode plate manufacturing process and lead-acid battery assembly process, thereby extending battery life.

本発明を詳述すれば次のとおりである。The present invention will be described in detail as follows.

ポリオレフィン系の合成樹脂と船酔化物のの鉛化合物の
微粉末および可塑剤とからなる原材料を加熱混練した後
所定の太さを有する繊維に加工、成形する。然る後可塑
剤を溶出あるいは抽出する。本発明に適用できる鉛化合
物とは、現在活物質の原料として一般に使用されている
鉛粉(約65乃至80%の酸化鉛、35乃至20%の金
属鉛からなる)や硫酸鉛、鉛丹、二酸化鉛等あるいはそ
れらの混−合物があげられる。このようにして得られた
合成繊維は、内部に均一に鉛化合物を保持している。さ
らにこの鉛化合物の周囲には、抽出された可塑剤によつ
て形成された微孔を有し電解液の浸透も容易である。従
つて、合成繊維中の鉛化合物もペー −ストを格子基体
に充填後通常の化成を行えば殆ど化成されるため、周囲
の活物質層と一体となるので格子基体と活物質との密着
性が著しく向上する。繊維の強風や活物質との密着性は
、樹脂や鉛化合物および可塑剤の配合比による変化する
A raw material consisting of a polyolefin synthetic resin, a fine powder of a seasick lead compound, and a plasticizer is heated and kneaded, and then processed and molded into fibers having a predetermined thickness. Thereafter, the plasticizer is eluted or extracted. Lead compounds that can be applied to the present invention include lead powder (consisting of approximately 65 to 80% lead oxide and 35 to 20% metallic lead), lead sulfate, red lead, which are currently commonly used as raw materials for active materials. Examples include lead dioxide and mixtures thereof. The synthetic fiber thus obtained uniformly retains the lead compound inside. Furthermore, the lead compound has micropores formed by the extracted plasticizer, allowing easy penetration of the electrolyte. Therefore, most of the lead compounds in the synthetic fibers will be chemically converted by performing normal chemical conversion after filling the lattice substrate with paste, and will become integrated with the surrounding active material layer, thereby improving the adhesion between the lattice substrate and the active material. is significantly improved. The adhesion of fibers to strong winds and active materials changes depending on the blending ratio of resin, lead compound, and plasticizer.

一般に繊維の強度を増そうとして樹脂の量を多くすると
活物質との密着性か低下し、活物質との密着性を向上さ
せようとして鉛化合物の量を多くすると繊維の強度は脆
化する。従つて、総合的には3成分の最適な配合割合の
範囲は、樹脂/鉛化合物/可塑剤=15〜30/8〜1
7/58〜75(いずれも重量%)である。実施例1 ペレット状の低密度ポリエチレン(25重量%)と鉛粉
〔酸化鉛(75%)と金属鉛(25%)の混合物を15
重量%〕およびペテロリウムオイル(6轍量%)をミキ
サーで混合した原材料を200±10にて加熱混練した
後押出成形した約3デニールの長繊維を得た。
Generally, if the amount of resin is increased in an attempt to increase the strength of the fiber, the adhesion with the active material will decrease, and if the amount of lead compound is increased in an attempt to improve the adhesion with the active material, the strength of the fiber will become brittle. Therefore, overall, the optimal blending ratio range of the three components is resin/lead compound/plasticizer = 15-30/8-1.
7/58 to 75 (all percentages by weight). Example 1 Pellet-shaped low-density polyethylene (25% by weight) and lead powder [a mixture of lead oxide (75%) and metallic lead (25%)]
[wt%]] and petroleum oil (6 rut weight) in a mixer, the raw materials were heated and kneaded at 200±10°C, and then extruded to obtain long fibers of about 3 denier.

然る後、繊維中の可塑剤をトリクロルエチレン溶液中に
て超音波抽出した。このようにして得られた合成繊維を
約1ミリの長さに裁断した。
Thereafter, the plasticizer in the fibers was extracted by ultrasonication in a trichlorethylene solution. The synthetic fiber thus obtained was cut into a length of about 1 mm.

これを鉛粉に対して0.0踵量%の割合で添加し、他は
従来と同様の所定の方法でペーストを練合後格子基体に
充填して極板を得た。実施例2 ペレット状の低密度ポリエチレン(25重量%)と鉛丹
(15重量%)およびペテロリウムオイル(6鍾量%)
をミキサーで混合した原材料を200±10′Cにて加
熱混練する。
This was added at a ratio of 0.0% by mass to the lead powder, and the paste was kneaded in the same predetermined manner as in the prior art, and then filled into a grid base to obtain an electrode plate. Example 2 Pellet-shaped low-density polyethylene (25% by weight), red lead (15% by weight) and petroleum oil (6% by weight)
The raw materials mixed in a mixer are heated and kneaded at 200±10'C.

然る後実施例1と同様方法で多孔性繊維を得、さらに鉛
粉に添加してペーストを練合後格子基体に充填して極板
を得た。次に本発明によつて得られた化成後の陽極板を
50C!Rの高さから表、裏交互に鉄板上に落下させた
時の活物質の脱落量は図面に示すとおりである。図面に
よつて明らかなる如く、本発明による鉛粉を保持せしめ
た繊維を添加した極板は活物質の脱落が少なく、活物質
強度が向上したことがわかる。また化成をしていない極
板においても同様の結果が得られた。
Thereafter, porous fibers were obtained in the same manner as in Example 1, and the paste was added to lead powder, kneaded, and then filled into a grid base to obtain an electrode plate. Next, the anode plate after chemical conversion obtained by the present invention was heated to 50C! The amount of active material falling off when dropped from the height R onto the iron plate alternately on the front and back sides is as shown in the drawing. As is clear from the drawings, it can be seen that in the electrode plate to which the fiber holding lead powder according to the present invention was added, the active material was less likely to fall off, and the strength of the active material was improved. Similar results were also obtained for electrode plates that were not chemically formed.

なお、図面に示される本発明による極板に添加した鉛粉
を保持せしめた合成繊維は、長さ、太さ、量のいずれも
従来の極板と同等にした。
The length, thickness, and amount of the synthetic fibers added to the electrode plate according to the present invention shown in the drawings to retain lead powder were the same as those of the conventional electrode plate.

図面において、Aは従来の極板、Bは本発明による極板
を夫々示す。上述せる如く、本発明によれば蓄電池の製
造工程における極板の活物質脱落による不良が大幅に減
少し、また、脱落した活物質による極板群下部での短絡
発生もなく、蓄電池の寿命性能が向上する等工業的価値
甚だ大なるものである。
In the drawings, A represents a conventional electrode plate, and B represents an electrode plate according to the present invention. As described above, according to the present invention, defects caused by falling off of active material from electrode plates during the manufacturing process of storage batteries are significantly reduced, and there is no occurrence of short circuits at the bottom of the electrode group due to fallen active material, which improves the life performance of storage batteries. The industrial value is enormous as it improves the

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

図面は本発明によつて得られた極板と従来の極板とを5
0dの高さから落下させた時の活物質の脱落量を示す比
較図である。 Aは従来の極板、Bは本発明による極板。
The drawing shows the electrode plate obtained by the present invention and the conventional electrode plate.
FIG. 2 is a comparison diagram showing the amount of active material falling off when dropped from a height of 0d. A is a conventional electrode plate, and B is an electrode plate according to the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリオレフィン系合成樹脂と鉛化合物の粉末および
可塑剤とからなる原材料を加熱混練した後所定の太さを
有する繊維状に成形後可塑剤を溶出あるいは押出して多
孔性を保持せしめ、多孔性を有する繊維を所定の長さに
裁断してペースト中に添加することを特徴とする鉛蓄電
池用極板の製造法。
1 Raw materials consisting of polyolefin synthetic resin, lead compound powder, and plasticizer are heated and kneaded, then formed into a fiber having a predetermined thickness, and the plasticizer is eluted or extruded to maintain porosity. A method for producing electrode plates for lead-acid batteries, characterized by cutting fibers into predetermined lengths and adding them to a paste.
JP55056485A 1980-04-28 1980-04-28 Manufacturing method of electrode plates for lead-acid batteries Expired JPS6054742B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55056485A JPS6054742B2 (en) 1980-04-28 1980-04-28 Manufacturing method of electrode plates for lead-acid batteries

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55056485A JPS6054742B2 (en) 1980-04-28 1980-04-28 Manufacturing method of electrode plates for lead-acid batteries

Publications (2)

Publication Number Publication Date
JPS56152165A JPS56152165A (en) 1981-11-25
JPS6054742B2 true JPS6054742B2 (en) 1985-12-02

Family

ID=13028397

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55056485A Expired JPS6054742B2 (en) 1980-04-28 1980-04-28 Manufacturing method of electrode plates for lead-acid batteries

Country Status (1)

Country Link
JP (1) JPS6054742B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6145565A (en) * 1984-08-09 1986-03-05 Yuasa Battery Co Ltd Storage battery
JPH0815081B2 (en) * 1987-06-19 1996-02-14 松下電器産業株式会社 Manufacturing method of electrode plate for lead-acid battery

Also Published As

Publication number Publication date
JPS56152165A (en) 1981-11-25

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