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JPS5851671B2 - Method for manufacturing base for lead-acid battery - Google Patents

Method for manufacturing base for lead-acid battery

Info

Publication number
JPS5851671B2
JPS5851671B2 JP54052978A JP5297879A JPS5851671B2 JP S5851671 B2 JPS5851671 B2 JP S5851671B2 JP 54052978 A JP54052978 A JP 54052978A JP 5297879 A JP5297879 A JP 5297879A JP S5851671 B2 JPS5851671 B2 JP S5851671B2
Authority
JP
Japan
Prior art keywords
lead
plasticizer
acid battery
substrate
active material
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
JP54052978A
Other languages
Japanese (ja)
Other versions
JPS55144661A (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 JP54052978A priority Critical patent/JPS5851671B2/en
Publication of JPS55144661A publication Critical patent/JPS55144661A/en
Publication of JPS5851671B2 publication Critical patent/JPS5851671B2/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
    • H01M4/64Carriers or collectors
    • H01M4/82Multi-step processes for manufacturing carriers for lead-acid accumulators
    • 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)
  • Cell Electrode Carriers And Collectors (AREA)

Description

【発明の詳細な説明】 本発明は鉛蓄電池用基体の製造方法の改良に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement in a method for manufacturing a base for a lead-acid battery.

従来鉛蓄電池の軽量化を図るため、極板となる基体の軽
量化が進められ、その軽量化のうち合成樹脂の活物質保
持体と鉛または鉛合金の集電体とからなる軽量化基体が
広く検討されている。
In order to reduce the weight of conventional lead-acid batteries, progress has been made to reduce the weight of the base material that serves as the electrode plate. Among these weight reductions, the lightweight base material consisting of a synthetic resin active material holder and a lead or lead alloy current collector has been developed. It is being widely considered.

合成樹脂を用いた基体は、通常の成形を行なったもので
は表面が滑らかなため、活物質との密着性が悪く、蓄電
池の組立時や使用時に基体から活物質が脱落し易い欠点
を有している。
Substrates made of synthetic resins that have been molded normally have a smooth surface, which results in poor adhesion to the active material, which has the disadvantage that the active material easily falls off the substrate when assembling or using the storage battery. ing.

−このため、基体の一部を構成する活物質保持体の格子
形状を複雑にしたり、表面に細かな傷をつげること等が
試みられたが何れも実用的ではない等の欠点を有してい
た。
- For this reason, attempts have been made to complicate the lattice shape of the active material holder that forms part of the substrate, or to make small scratches on the surface, but these methods have drawbacks such as being impractical. Ta.

本発明は上記の点に鑑み、合成樹脂の格子体と活物質と
の密着性を向上せしめるものである。
In view of the above points, the present invention improves the adhesion between a synthetic resin lattice and an active material.

即ち、本発明は、合成樹脂の格子体に多孔性を保持せし
めることで、格子体の表面に均一に凹凸を形成せしめて
、活物質との密着性を向上せしめんとするものである。
That is, the present invention aims to maintain porosity in a synthetic resin lattice body, thereby forming irregularities uniformly on the surface of the lattice body, thereby improving the adhesion with the active material.

本発明においては、ポリオレフィン系合成樹脂と充填剤
および可塑剤とからなる原材料を加熱混練した後集電体
と射出成形または加圧成形して集電体と一体化する。
In the present invention, a raw material consisting of a polyolefin synthetic resin, a filler, and a plasticizer is heated and kneaded, and then injection molded or pressure molded with a current collector to integrate it with the current collector.

然る後可塑剤あるいは可塑剤と充填剤を溶出あるいは抽
出して基体に小孔を形成せしめる。
Thereafter, the plasticizer or plasticizer and filler are eluted or extracted to form small pores in the substrate.

か(して得られた基体は、表面に均一に凹凸が形成され
るため、ペーストを充填すると、基体表面の小孔にペー
ストが理詰されるため、その後の工程にて極板の乾燥、
化成を施した後も基体と活物質との密着性は良好になる
The substrate obtained by this process has uniform irregularities on its surface, so when it is filled with paste, the paste is packed into the small holes on the surface of the substrate, so in the subsequent process the electrode plate is dried and
Even after chemical conversion, the adhesion between the substrate and the active material is good.

本発明において、形成される小孔の大きさ量および格子
体の強度は、充填剤の粒子径や可塑剤の割合で変えるこ
とができる。
In the present invention, the size of the small pores formed and the strength of the lattice body can be changed by changing the particle size of the filler and the proportion of the plasticizer.

実際には孔径は約10ミクロン以下の大きさの範囲が可
能であるが、現在使用されている鉛粉の粒子は0.5乃
至1ミクロy程度のものが多いので、理想的には1ミク
ロン以上あった方が、密着は良好である。
In reality, the pore diameter can be within a range of about 10 microns or less, but most of the lead powder particles currently used are around 0.5 to 1 micron, so ideally the pore diameter is about 1 micron. The more it is, the better the adhesion is.

また密着性を向上させようとして、充填剤の量を多くす
ると格子体は脆化し、強度を増そうとして合成樹脂の量
を多くすると密着性が低下するため、三成分の配合の最
適範囲は合成樹脂/充填剤/可塑剤=15〜30/8〜
17158〜75である。
Furthermore, if the amount of filler is increased in an attempt to improve adhesion, the lattice will become brittle, and if the amount of synthetic resin is increased in an attempt to increase strength, the adhesion will decrease. Resin/filler/plasticizer=15~30/8~
17158-75.

本発明の一実施例を説明する。An embodiment of the present invention will be described.

実施例 1 ペレット状の低密度ポリエチレン25重量%とシリカの
粉末平均粒子径1.5μ、15重量%と可塑剤ジオクチ
ルフタレート60重量%とミキサーで混合した原材料を
200±10℃にて加熱混練する。
Example 1 A raw material prepared by mixing 25% by weight of pelletized low-density polyethylene, 15% by weight of silica powder with an average particle size of 1.5μ, and 60% by weight of plasticizer dioctyl phthalate in a mixer is heated and kneaded at 200±10°C. .

然る後鉛−アンチモン合金からなる集電体と射出成形し
て集電体と一体化し、続いてトリクロルエチレン溶液中
にて超音波抽出により可塑剤な除去して基体を得た。
Thereafter, it was integrated with a current collector by injection molding with a current collector made of a lead-antimony alloy, and then the plasticizer was removed by ultrasonic extraction in a trichlorethylene solution to obtain a substrate.

実施例 2 ペレット状の低密度ポリエチレン25重量%とカーボン
ブラック5重量%、シリカ粉末10重量%、およびペテ
ロリウムオイル60重量%とをミキサーで混合した原材
料を200±10℃にて加熱混練する。
Example 2 A raw material prepared by mixing 25% by weight of pelletized low density polyethylene, 5% by weight of carbon black, 10% by weight of silica powder, and 60% by weight of petroleum oil in a mixer is heated and kneaded at 200±10°C.

これを鉛−カルシウム合金からなる集電体と射出成形し
て集電体と一体化しtも可塑剤はトリクロルエチレンで
抽出し基体を得た。
This was injection molded with a current collector made of a lead-calcium alloy to integrate it with the current collector, and the plasticizer was extracted with trichlorethylene to obtain a base.

上記各実施例の如くして得られた基体は、従来の基体に
比べて、活物質との密着性が優れており、従来の基体の
ように、形状を複雑にする必要はな(、基体の製造が容
易になった。
The substrates obtained as in each of the above examples have superior adhesion to the active material compared to conventional substrates, and unlike conventional substrates, there is no need to complicate the shape. has become easier to manufacture.

また蓄電池の使用中や組立時等における活物質の脱落が
減少したため、極板群の底部等における短絡の発生も減
少して寿命を延長することができた。
Furthermore, since the active material is less likely to fall off during use or assembly of the storage battery, the occurrence of short circuits at the bottom of the electrode plate group is also reduced, thereby extending the life of the battery.

さらに基体の小孔中に電解液が侵透するため、従来の基
体に比べて電気抵抗が小さくなり、本発明による基体を
用いた電池や低温高率放電性能は従来の基体を用いた電
池に比べて電圧特性が優れている。
Furthermore, because the electrolyte penetrates into the small pores of the substrate, the electrical resistance is lower than that of conventional substrates, and the batteries using the substrate of the present invention and the low-temperature high-rate discharge performance are better than those using conventional substrates. It has superior voltage characteristics compared to other products.

上述せる如く、本発明は基体と活物質との密着性が優れ
た基体を容易に製造することができ、而も寿命を延長な
らしめ、また電圧特性が向上する等工業的価値甚だ大な
るものである。
As mentioned above, the present invention enables the easy production of a substrate with excellent adhesion between the substrate and the active material, and has great industrial value such as extending the life and improving voltage characteristics. It is.

Claims (1)

【特許請求の範囲】[Claims] 1 ポリオレフィン系樹脂と充填剤および可塑剤からな
る原材料を加熱混練した後鉛または鉛合金からなる集電
体と射出または加圧成形して一体化し、然る後可塑剤あ
るいは可塑剤と充填剤とを溶出もしくは抽出して多孔を
形成せしめたことを特徴とする鉛蓄電池用基体の製造方
法。
1 After heating and kneading the raw materials consisting of polyolefin resin, filler and plasticizer, they are integrated by injection or pressure molding with a current collector made of lead or lead alloy, and then the plasticizer or plasticizer and filler are combined. A method for producing a base for a lead-acid battery, characterized in that pores are formed by eluting or extracting.
JP54052978A 1979-04-27 1979-04-27 Method for manufacturing base for lead-acid battery Expired JPS5851671B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP54052978A JPS5851671B2 (en) 1979-04-27 1979-04-27 Method for manufacturing base for lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP54052978A JPS5851671B2 (en) 1979-04-27 1979-04-27 Method for manufacturing base for lead-acid battery

Publications (2)

Publication Number Publication Date
JPS55144661A JPS55144661A (en) 1980-11-11
JPS5851671B2 true JPS5851671B2 (en) 1983-11-17

Family

ID=12929981

Family Applications (1)

Application Number Title Priority Date Filing Date
JP54052978A Expired JPS5851671B2 (en) 1979-04-27 1979-04-27 Method for manufacturing base for lead-acid battery

Country Status (1)

Country Link
JP (1) JPS5851671B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5738691A (en) * 1997-04-28 1998-04-14 Valence Technology, Inc. Ultrasonic extraction of plasticizer from electrochemical cells

Also Published As

Publication number Publication date
JPS55144661A (en) 1980-11-11

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