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JPS6325461B2 - - Google Patents
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JPS6325461B2 - - Google Patents

Info

Publication number
JPS6325461B2
JPS6325461B2 JP57036629A JP3662982A JPS6325461B2 JP S6325461 B2 JPS6325461 B2 JP S6325461B2 JP 57036629 A JP57036629 A JP 57036629A JP 3662982 A JP3662982 A JP 3662982A JP S6325461 B2 JPS6325461 B2 JP S6325461B2
Authority
JP
Japan
Prior art keywords
lead
coating
film
temperature
molten
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
JP57036629A
Other languages
Japanese (ja)
Other versions
JPS58154174A (en
Inventor
Sadao Furuya
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 JP57036629A priority Critical patent/JPS58154174A/en
Publication of JPS58154174A publication Critical patent/JPS58154174A/en
Publication of JPS6325461B2 publication Critical patent/JPS6325461B2/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)

Description

【発明の詳細な説明】 本発明は鉛蓄電池の極板に使用する格子体の改
良に関し、合成樹脂製格子体を溶融鉛合金に浸漬
し素早く引き上げることによつて格子体の表面に
鉛の薄被膜を形成する方法において、導電性を必
要とする部分にのみ鉛被膜を形成させて鉛の使用
量を節減し、以つて、格子体、延いては鉛蓄電池
の軽量化を一層促進することを目的とするもので
ある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to the improvement of grids used in the electrode plates of lead-acid batteries, and involves coating a synthetic resin grid with a thin layer of lead on the surface of the grid by immersing a synthetic resin grid in molten lead alloy and quickly pulling it up. In the method of forming the film, it is possible to reduce the amount of lead used by forming the lead film only on the parts that require conductivity, thereby further promoting weight reduction of the lattice body and, by extension, the weight of the lead-acid battery. This is the purpose.

鉛蓄電池の軽量化は、自動車用においては燃費
向上のため、電気自動車においては走行距離延伸
のため、ポータブル機器においては持ち運び易さ
のため、その要望は大きい。そこで極板の鉛格子
を鋳造または鉛板金製のものから、鉛の比重11.4
の約1/10しかない合成樹脂製に代えて、格子体に
要求される機械的強度と、活物質保持の条件を満
たし、今一つの条件である電気の伝導性について
は、合成樹脂格子体を溶融鉛に一瞬浸漬するか、
(以下、浸漬法と云う)または溶融鉛を掛けるか
して、合成樹脂の表面に鉛被膜を形成していた。
この方法によると製造工程が比較的簡単で連続生
産をすることも可能なので生産性も高めることが
できた。
There is a strong desire to reduce the weight of lead-acid batteries for purposes such as improving fuel efficiency in automobiles, extending mileage in electric vehicles, and making them easier to carry in portable devices. Therefore, the lead grid of the electrode plate is cast or made of lead sheet metal, and the specific gravity of lead is 11.4.
Instead of synthetic resin, which is only about 1/10 of by momentary immersion in molten lead, or
(hereinafter referred to as the immersion method) or by applying molten lead to form a lead film on the surface of the synthetic resin.
According to this method, the manufacturing process is relatively simple and continuous production is possible, so productivity can be increased.

第1図aは上記従来の方法で製造した合成樹脂
格子体を示す。図中、黒く塗り潰した部分は前記
浸漬法により鉛被膜を形成した部分を表わす。し
かしよく考えてみると、第1図aのものにもなお
鉛被膜を節約できる部分が残されている。
FIG. 1a shows a synthetic resin lattice body manufactured by the above-mentioned conventional method. In the figure, the blacked out areas represent the areas where the lead coating was formed by the above-mentioned dipping method. However, if you think about it carefully, there are still parts in the structure shown in Figure 1a where the lead coating can be saved.

第1図bは、合成樹脂格子体に必要最少限の鉛
被膜を施したものの一例を示し、黒く塗り潰した
部分が鉛で被覆されている。このようなものを浸
漬法で実現するには、等しく浸漬法を適用しても
鉛被膜が付着する表面と、付着しない表面の二つ
を作り出す必要がある。
FIG. 1b shows an example of a synthetic resin lattice body coated with the minimum necessary amount of lead, with the blacked-out portions being coated with lead. In order to realize something like this using the immersion method, it is necessary to create two surfaces: one on which the lead film will adhere even if the immersion method is applied, and one on which it will not.

本発明は以上二つの表面を実現して、鉛被膜を
最小限に抑え、軽量化を促進する方法に関するも
のである。
The present invention relates to a method of achieving the above two surfaces to minimize lead coating and promote weight reduction.

以下図面を参照しつつこの方法を三つの実施例
について詳細に説明する。
This method will be described in detail below with reference to three embodiments with reference to the drawings.

(1) 第2図は第1実施例の説明図で、Aは直径2
mmの合成樹脂、ポリプロピレンで表面が平滑な
もの、Bは同径、同材質で、その表面には細か
な突起を一面に設けたものである。このAとB
を温度337℃の溶融鉛中に0.4秒浸漬して引き上
げると、Aの方は厚さ30μmの鉛被膜を付着し
ていたが、Bの方は無被膜であつた。これはA
の方は合成樹脂にこれを取り巻く溶融鉛が熱を
奪われ合成樹脂の表面に接近した鉛が凝固付着
した瞬間に引き上げたものであり、Bの方は微
細な突起が先に溶融して凝固鉛の付着を妨げた
ものと考えられる。
(1) Figure 2 is an explanatory diagram of the first embodiment, where A is the diameter 2
mm synthetic resin or polypropylene with a smooth surface, B is the same diameter and made of the same material, and has fine protrusions all over its surface. This A and B
When it was immersed in molten lead at a temperature of 337°C for 0.4 seconds and pulled out, it was found that A had a 30 μm thick lead coating, but B had no coating. This is A
In case B, the heat is absorbed by the molten lead surrounding the synthetic resin, and the lead approaches the surface of the synthetic resin and is pulled up at the moment it solidifies and adheres to it. In case B, the fine protrusions melt first and solidify. It is thought that this prevented the adhesion of lead.

(2) 第3図は第2の実施例の説明図で、Aは厚さ
2mm,巾5mm,長さ30mmのポリプロピレンでそ
の表面に穴と溝を多数穿設したもの、Bは同一
の材料で穴・溝がなく表面が平滑なものであ
る。このAとBを温度345℃の溶融鉛中に0.4秒
間浸漬して引き上げると、Aの方には鉛被膜を
形成し、Bの方は無被膜であつた。これはAの
方は穴・溝中で素早く凝固した鉛は溶融鉛との
距離が遠くて熱が伝わりにくいため再溶融に時
間がかかると共に隣接域にも影響するのに対
し、Bの方は一旦は凝固した鉛が引き上げる時
には再溶融したものと考えられる。
(2) Figure 3 is an explanatory diagram of the second embodiment, where A is polypropylene with a thickness of 2 mm, width of 5 mm, and length of 30 mm with many holes and grooves drilled on its surface, and B is the same material. It has a smooth surface with no holes or grooves. When A and B were immersed in molten lead at a temperature of 345° C. for 0.4 seconds and pulled out, A had a lead coating, while B had no coating. This is because in case A, the lead that solidifies quickly in the hole/groove is far away from the molten lead, making it difficult for heat to transfer, so it takes time to remelt it and also affects adjacent areas, whereas in case B, It is thought that the once solidified lead was remelted when pulled up.

以上(1),(2)の実施例は、同一材質の二つの合成
樹脂材の表面形態を変えることによつて鉛被膜を
形成したり、しなかつたりするものであつたが、
次に異質の合成樹脂の間で行なう実施例を示す。
In the examples (1) and (2) above, a lead coating was formed or not formed by changing the surface morphology of two synthetic resin materials of the same material.
Next, an example will be shown in which the method is carried out between different types of synthetic resins.

(3) 第4図は第3の実施例の説明図で、Aは直径
2mmのポリプロピレン、Bは同寸法のA.B.S
(アクリルニトル・ブタジエン・スチレン樹脂)
である。このAとBを温度340℃の溶融鉛中に
0.4秒間浸漬して引き上げるとAの方には鉛被
膜を形成したが、Bの方は無被膜であつた。こ
れはA.B.Sの方がポリプロピレンより溶融温度
が低いため、表面が早く溶融して鉛被膜の付着
を妨げるのに対し、ポリプロピレンの方は表面
が溶融し始める前に引き上げられるので鉛被膜
を付着しているものと考えられる。
(3) Figure 4 is an explanatory diagram of the third embodiment, where A is polypropylene with a diameter of 2 mm, and B is ABS with the same size.
(Acrylic nitrile, butadiene, styrene resin)
It is. These A and B are placed in molten lead at a temperature of 340℃.
When the sample was immersed for 0.4 seconds and pulled up, a lead coating was formed on the sample A, but no coating was formed on the sample B. This is because ABS has a lower melting temperature than polypropylene, so the surface melts quickly and prevents the lead film from adhering to it, whereas polypropylene is pulled up before the surface starts to melt, making it difficult for the lead film to adhere. It is thought that there are.

以上実施例(1),(2),(3)の場合において鉛被膜を
形成するに要する溶融鉛温度と浸漬時間の関係を
夫々第5図,第6図,第7図に示す。
The relationship between the molten lead temperature and the immersion time required to form a lead film in the above Examples (1), (2), and (3) is shown in FIGS. 5, 6, and 7, respectively.

第5図において実線で囲まれた範囲は第2図の
Aに被膜を形成する鉛温度と浸漬時間、点線(一
部実線と重複、以下同じ)で囲まれた範囲は同B
に被膜を形成する鉛温度と浸漬時間を示す。
In Fig. 5, the range surrounded by a solid line is the lead temperature and immersion time for forming a film in A of Fig. 2, and the range surrounded by a dotted line (partially overlapping with the solid line, the same applies hereinafter) is the same as B.
shows the lead temperature and immersion time to form a film.

同様に第6図において実線で囲まれた範囲はB
に、点線で囲まれた範囲はAに夫々被膜を形成す
る鉛温度と浸漬時間を示す。
Similarly, in Figure 6, the range surrounded by a solid line is B
The range surrounded by dotted lines shows the lead temperature and immersion time for forming the respective films in A.

更に第7図において実線で囲まれた範囲はA
に、点線で囲まれた範囲はBに夫々被膜を形成す
る鉛温度と浸漬時間を示す。
Furthermore, the range surrounded by a solid line in Fig. 7 is A.
The range surrounded by dotted lines shows the lead temperature and immersion time for forming a film on B, respectively.

以上第5図乃至第7図を総合すると、三つの場
合を通じて、実線域と点線域の差域即ちa域の溶
融鉛温度と浸漬時間の範囲でAのみに鉛被膜を形
成しBは無被膜とすることができる。
Combining the above figures 5 to 7, in the three cases, a lead coating is formed only in A, and no coating is formed in B in the range of molten lead temperature and immersion time in the difference area between the solid line area and the dotted line area, that is, area a. It can be done.

従つて、第1図bにおいて黒く塗り潰した部分
をA、それ以外の部分をBで構成し、このA,B
に対応したa域の温度と時間で浸漬法を行なえば
第1図bで塗り潰した部分にのみ鉛被膜を形成す
ることができ、比重の大きい鉛の使用を最少限に
抑えることができる。
Therefore, in Fig. 1b, the blacked out part is made up of A, and the other parts are made up of B, and these A, B
If the immersion method is carried out at a temperature and time in range a corresponding to , it is possible to form a lead film only in the shaded area in FIG.

以上説明したように本発明によれば鉛蓄電池極
板格子体の鉛使用量を必要最少限に止めて軽量化
に資することができると共に大量生産にも貢献す
る効果は顕著である。
As explained above, according to the present invention, the amount of lead used in the lead-acid battery electrode grid can be kept to the minimum necessary, contributing to weight reduction, and the effect of contributing to mass production is remarkable.

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

第1図aは従来の製造法による鉛蓄電池極板格
子体の正面図、第1図bは本発明1実施例により
製造された格子体の正面図、第2図は本発明の第
1実施例の説明図、第3図は同第2実施例の説明
図、第4図は同第3実施例の説明図、第5図,第
6図,第7図は夫々第2図,第3図,第4図の場
合における鉛被膜形成に必要な溶融鉛温度と浸漬
時間を示す線図である。
FIG. 1a is a front view of a lead-acid battery plate lattice manufactured by a conventional manufacturing method, FIG. 1b is a front view of a lattice manufactured according to the first embodiment of the present invention, and FIG. FIG. 3 is an explanatory diagram of the second embodiment, FIG. 4 is an explanatory diagram of the third embodiment, and FIGS. 5, 6, and 7 are diagrams of FIGS. FIG. 5 is a diagram showing the molten lead temperature and immersion time necessary for forming a lead film in the case of FIGS.

Claims (1)

【特許請求の範囲】[Claims] 1 表面形態あるいは材質の異なる耐酸性合成樹
脂を組み合わせてなる構造体を溶融した鉛または
鉛合金に浸漬するか、または同構造体の上から溶
融した鉛または鉛合金を流しかけるなどにより構
造体表面に対する鉛または鉛合金被膜付着力の有
無を利用して、構造体表面に選択的に鉛または鉛
合金の被膜を形成した極板格子体を備えることを
特徴とする鉛蓄電池の製造法。
1. The surface of the structure is immersed in molten lead or lead alloy, or by pouring molten lead or lead alloy over the structure. 1. A method for manufacturing a lead-acid battery, comprising: an electrode plate grid body on which a lead or lead alloy coating is selectively formed on the surface of the structure by utilizing the adhesion of the lead or lead alloy coating to the lead or lead alloy coating.
JP57036629A 1982-03-10 1982-03-10 Manufacture of lead-acid battery Granted JPS58154174A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57036629A JPS58154174A (en) 1982-03-10 1982-03-10 Manufacture of lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57036629A JPS58154174A (en) 1982-03-10 1982-03-10 Manufacture of lead-acid battery

Publications (2)

Publication Number Publication Date
JPS58154174A JPS58154174A (en) 1983-09-13
JPS6325461B2 true JPS6325461B2 (en) 1988-05-25

Family

ID=12475117

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57036629A Granted JPS58154174A (en) 1982-03-10 1982-03-10 Manufacture of lead-acid battery

Country Status (1)

Country Link
JP (1) JPS58154174A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60157159A (en) * 1984-01-26 1985-08-17 Shin Kobe Electric Mach Co Ltd Manufacture of plate for lead storage battery

Also Published As

Publication number Publication date
JPS58154174A (en) 1983-09-13

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