JPH0322024B2 - - Google Patents

Info

Publication number
JPH0322024B2
JPH0322024B2 JP57006294A JP629482A JPH0322024B2 JP H0322024 B2 JPH0322024 B2 JP H0322024B2 JP 57006294 A JP57006294 A JP 57006294A JP 629482 A JP629482 A JP 629482A JP H0322024 B2 JPH0322024 B2 JP H0322024B2
Authority
JP
Japan
Prior art keywords
lead
synthetic resin
lead alloy
thin film
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.)
Expired - Lifetime
Application number
JP57006294A
Other languages
Japanese (ja)
Other versions
JPS58123863A (en
Inventor
Yukihiro Onoda
Kenji Kobayashi
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 JP57006294A priority Critical patent/JPS58123863A/en
Publication of JPS58123863A publication Critical patent/JPS58123863A/en
Publication of JPH0322024B2 publication Critical patent/JPH0322024B2/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
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/64Carriers or collectors
    • H01M4/70Carriers or collectors characterised by shape or form
    • H01M4/72Grids
    • H01M4/73Grids for lead-acid accumulators, e.g. frame plates
    • 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)
  • Coating With Molten Metal (AREA)

Description

【発明の詳細な説明】 本発明は、鉛蓄電池に使用される鉛または鉛合
金と合成樹脂を複合した格子体の製造法に関する
ものであり、その目的とするところは耐衝撃性が
あり、耐久性に優れた長寿命で軽量な極板を生産
性よく製造することにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a lattice made of a composite of lead or lead alloy and synthetic resin used in lead-acid batteries, and its purpose is to have impact resistance and durability. The goal is to manufacture long-life, lightweight electrode plates with good productivity.

通常、鉛蓄電池の格子体は鉛合金を鋳造するこ
とにより製造され、軽量薄形化が図られてきた
が、鋳造およびその後工程での問題から、鋳造格
子の軽量化には一定の限度があつた。
Normally, the grid bodies of lead-acid batteries are manufactured by casting lead alloy to make them lighter and thinner, but due to problems in casting and subsequent processes, there are certain limits to the weight reduction of cast grids. Ta.

そこで、導電性の必要な部分にのみ鉛合金を使
用し、ペースト状作用物質を保持する部分には比
重が鉛合金の1/10以下である合成樹脂を使用し
た、いわゆる鉛合金−合成樹脂の複合格子体が考
えられてきた。
Therefore, lead alloy is used only in the parts that require conductivity, and synthetic resin with specific gravity less than 1/10 of lead alloy is used in the part that holds the paste-like active substance, so-called lead alloy-synthetic resin. Composite lattices have been considered.

例えば、特開昭0−8037号公報に見られるよう
に、鉛合金で鋳造された導電部分を、合成樹脂の
成型金型に挿入して合成樹脂と一体成型した鉛合
金−合成樹脂複合格子体が提案されている。ま
た、実公昭43−3535号公報では、合成樹脂の格子
体と鉛合金製有孔板とを積層接着した鉛合金−合
成樹脂複合格子体が提案されている。
For example, as seen in Japanese Unexamined Patent Publication No. 0-8037, a lead alloy-synthetic resin composite lattice body is formed by inserting a conductive part cast from a lead alloy into a synthetic resin mold and integrally molding it with the synthetic resin. is proposed. Further, Japanese Utility Model Publication No. 43-3535 proposes a lead alloy-synthetic resin composite lattice body in which a synthetic resin lattice body and a lead alloy perforated plate are laminated and bonded.

しかし、これらはいずれも製造工程が複雑であ
るばかりでなく、導電性を有する鉛合金部分が細
い骨や薄い板であるため、わん曲や変形を起こし
やすく、取扱いも困難である。そのため生産性が
悪く、大量生産には適さない欠点があつた。
However, all of these have complicated manufacturing processes, and because the conductive lead alloy portion is made of thin bones or thin plates, they are easily bent or deformed and are difficult to handle. As a result, productivity was low and it was not suitable for mass production.

本発明は、これらの欠点を解消しようとするも
ので、鉛蓄電池に用いる格子体は、耐酸性を有す
る熱可塑性合成樹脂からなる格子構造体を溶融し
た鉛または鉛合金に浸漬するか、あるいは格子構
造体の上から溶融した鉛または鉛合金をかけてか
ら、所定時間、例えば1〜10秒間空気中に放置
し、ついて冷却することにより、格子構造体の表
面に鉛または鉛合金の薄膜を形成するとともに、
この薄膜の表面の一部に格子構造体の溶融した合
成樹脂をはみ出させて微小突起を形成させたもの
である。
The present invention aims to eliminate these drawbacks, and the lattice structure used in lead-acid batteries is made by immersing a lattice structure made of acid-resistant thermoplastic synthetic resin in molten lead or lead alloy, or by immersing a lattice structure made of acid-resistant thermoplastic synthetic resin in molten lead or a lead alloy. A thin film of lead or lead alloy is formed on the surface of the lattice structure by pouring molten lead or lead alloy onto the structure, leaving it in the air for a predetermined period of time, e.g. 1 to 10 seconds, and cooling it. At the same time,
The molten synthetic resin of the lattice structure is made to protrude from a part of the surface of this thin film to form minute protrusions.

以下に本発明の実施例を説明する。 Examples of the present invention will be described below.

第1図に示す従来の鋳造格子体と同様な形にポ
リプロピレンで成型された格子構造体1を335℃
に温度コントロールされた溶融鉛中に0.3秒浸漬
後引き上げて、5秒間放置した後に冷水にて冷却
する。
A lattice structure 1 molded from polypropylene in the same shape as the conventional cast lattice body shown in Fig. 1 was heated at 335°C.
It was immersed in molten lead whose temperature was controlled for 0.3 seconds, then pulled out, left to stand for 5 seconds, and then cooled with cold water.

これにより、ポリプロピレン格子構造体1の全
周囲に約200μの厚さの純鉛薄膜2と、薄膜表面
の複数個所にポリプロピレンの微小突起3を形成
することができた。その詳細を第2図に示す。
As a result, it was possible to form a pure lead thin film 2 with a thickness of approximately 200 μm around the entire circumference of the polypropylene lattice structure 1 and polypropylene microprotrusions 3 at multiple locations on the surface of the thin film. The details are shown in Figure 2.

ポリプロピレン製格子構造体を溶融鉛に浸漬す
ると表面のポリプロピレンは溶融し、周辺の鉛は
ポリプロピレンに熱をうばわれて凝固しようとす
る。この状態で引き上げて冷却すると、周囲の鉛
が薄膜状で凝固し、その凝集圧によつて溶融した
表面のポリプロピレンが周囲の薄膜の一部をつき
破つて外にはみ出る。このはみ出たポリプロピレ
ンは、冷却・凝固して第2図Bの如く微小突起3
を形成する。
When a polypropylene lattice structure is immersed in molten lead, the polypropylene on the surface melts, and the surrounding lead tends to solidify due to the heat absorbed by the polypropylene. When it is pulled up and cooled in this state, the surrounding lead solidifies in the form of a thin film, and due to the cohesive pressure, the molten polypropylene on the surface breaks through part of the surrounding thin film and protrudes outside. This protruding polypropylene is cooled and solidified to form microprotrusions 3 as shown in Figure 2B.
form.

したがつて、本発明は使用する合成樹脂は、ポ
リプロピレンに限らず熱可塑性樹脂であればよ
く、例えばポリエチレン、ポリ塩化ビニルなどを
使用することができる。また溶融鉛は純鉛の他、
鉛合金でも使用可能であり、327〜350℃の温度で
0.1〜1秒間浸漬した後に引き上げて所定時間例
えば1〜10秒間空気中に放置し、ついで水冷する
条件が最良であつた。この場合、放置時間がこれ
よりも長いと樹脂は軟くなり、格子形状がくずれ
て製造できなくなる。一方、放置時間が短いと、
薄膜2の外への必要な合成樹脂のはみ出しが得ら
れなかつた。なお溶融鉛合金は合成樹脂の上部か
らかけても、浸漬と同様な効果が得られた。
Therefore, the synthetic resin used in the present invention is not limited to polypropylene, but may be any thermoplastic resin, such as polyethylene, polyvinyl chloride, etc. In addition to pure lead, molten lead
Also available in lead alloys, at temperatures of 327-350℃
The best condition was to immerse it for 0.1 to 1 second, then pull it out, leave it in the air for a predetermined period of time, for example, 1 to 10 seconds, and then cool it with water. In this case, if the standing time is longer than this, the resin will become soft and the lattice shape will collapse, making it impossible to manufacture. On the other hand, if the exposure time is short,
The necessary protrusion of the synthetic resin to the outside of the thin film 2 could not be obtained. Note that the same effect as immersion was obtained even when the molten lead alloy was applied from above the synthetic resin.

第3図に従来の鉛鋳造格子体を使用した電池A
と、本発明の鉛−合成樹脂複合格子体を使用した
電池Bのサイクル寿命試験結果を示す。本発明の
鉛−合成樹脂複合格子体を使用した電池Bは従来
の鉛鋳造格子体と比較して寿命が優れている。
Figure 3 shows battery A using a conventional lead casting grid.
and shows the cycle life test results of battery B using the lead-synthetic resin composite grid of the present invention. Battery B, which uses the lead-synthetic resin composite grid of the present invention, has a superior lifespan compared to the conventional cast lead grid.

このような本発明の鉛合金−合成樹脂複合格子
体は、次のような効果を得ることができる。
The lead alloy-synthetic resin composite lattice of the present invention can provide the following effects.

(1) 合成樹脂の微小突起3の押え作用によつて鉛
または鉛合金薄膜2と格子構造体1との密着が
よく、薄膜2がはがれにくい堅ろうな格子体が
形成できる。
(1) Due to the pressing action of the synthetic resin microprotrusions 3, the lead or lead alloy thin film 2 and the lattice structure 1 are in close contact with each other, and a strong lattice structure in which the thin film 2 is difficult to peel off can be formed.

(2) 合成樹脂の微小突起3を設けたことにより、
活物質と格子体との密着性が良くなり活物質の
脱落が少ない強固な極板を作ることができる。
(2) By providing minute protrusions 3 made of synthetic resin,
The adhesion between the active material and the lattice is improved, and a strong electrode plate with less chance of active material falling off can be produced.

(3) 本発明の格子体の重量は、従来の鋳造格子体
のそれに比べて約1/10になり、電池を軽量化す
ることができる。
(3) The weight of the lattice body of the present invention is approximately 1/10 that of a conventional cast lattice body, making it possible to reduce the weight of the battery.

(4) 本発明の製造法によれば、従来の鉛合金−合
成樹脂複合格子体に比較して製造工程も簡単で
あり、生産性よく製造できる。
(4) According to the manufacturing method of the present invention, the manufacturing process is simpler than that of conventional lead alloy-synthetic resin composite lattice bodies, and it can be manufactured with high productivity.

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

第1図は本発明に使用した合成樹脂格子体を示
す図、第2図Aは第1図に示した合成樹脂格子構
造体に鉛薄膜を付着し、その一後の被覆をはがし
た本発明の実施例における格子体であり、Bはそ
の部分拡大図、第3図は同格子体を用いた電池の
サイクル寿命特性を示す。 1……熱可塑性合成樹脂からなる格子構造体、
2……純鉛または鉛合金薄膜、3……合成樹脂の
微小突起。
Figure 1 is a diagram showing the synthetic resin lattice structure used in the present invention, and Figure 2A is a diagram showing the synthetic resin lattice structure shown in Figure 1 with a lead thin film attached and the subsequent coating removed. B is a partially enlarged view of the lattice body in an example of the invention, and FIG. 3 shows the cycle life characteristics of a battery using the lattice body. 1... Lattice structure made of thermoplastic synthetic resin,
2...Pure lead or lead alloy thin film, 3...Synthetic resin minute protrusions.

Claims (1)

【特許請求の範囲】[Claims] 1 耐酸性を有する熱可塑性合成樹脂からなる格
子構造体1を溶融した鉛または鉛合金に浸漬する
か、あるいは格子構造体1の上から溶融した鉛ま
たは鉛合金をかけてから空気中に放置し、ついで
冷却することにより、格子構造体1の表面に鉛又
は鉛合金の薄膜2を形成し、この薄膜2の表面の
一部に格子構造体の合成樹脂をはみ出させて微小
突起3を形成することを特徴とする鉛蓄電池用格
子体の製造法。
1 A grid structure 1 made of acid-resistant thermoplastic synthetic resin is immersed in molten lead or lead alloy, or molten lead or lead alloy is poured over the grid structure 1 and then left in the air. Then, by cooling, a thin film 2 of lead or lead alloy is formed on the surface of the lattice structure 1, and the synthetic resin of the lattice structure is made to protrude from a part of the surface of this thin film 2 to form minute protrusions 3. A method for manufacturing a grid for lead-acid batteries characterized by the following.
JP57006294A 1982-01-18 1982-01-18 Manufacture of grid for lead storage battery Granted JPS58123863A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57006294A JPS58123863A (en) 1982-01-18 1982-01-18 Manufacture of grid for lead storage battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57006294A JPS58123863A (en) 1982-01-18 1982-01-18 Manufacture of grid for lead storage battery

Publications (2)

Publication Number Publication Date
JPS58123863A JPS58123863A (en) 1983-07-23
JPH0322024B2 true JPH0322024B2 (en) 1991-03-26

Family

ID=11634352

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57006294A Granted JPS58123863A (en) 1982-01-18 1982-01-18 Manufacture of grid for lead storage battery

Country Status (1)

Country Link
JP (1) JPS58123863A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9763488B2 (en) 2011-09-09 2017-09-19 Riddell, Inc. Protective sports helmet
US9788591B2 (en) 2007-04-16 2017-10-17 Riddell, Inc. Quick release connector

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9788591B2 (en) 2007-04-16 2017-10-17 Riddell, Inc. Quick release connector
US9763488B2 (en) 2011-09-09 2017-09-19 Riddell, Inc. Protective sports helmet

Also Published As

Publication number Publication date
JPS58123863A (en) 1983-07-23

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