JPS6054741B2 - Manufacturing method of electrode plates for lead-acid batteries - Google Patents
Manufacturing method of electrode plates for lead-acid batteriesInfo
- Publication number
- JPS6054741B2 JPS6054741B2 JP55056484A JP5648480A JPS6054741B2 JP S6054741 B2 JPS6054741 B2 JP S6054741B2 JP 55056484 A JP55056484 A JP 55056484A JP 5648480 A JP5648480 A JP 5648480A JP S6054741 B2 JPS6054741 B2 JP S6054741B2
- Authority
- JP
- Japan
- Prior art keywords
- lead
- fibers
- active material
- plasticizer
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- 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
成繊維状に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a synthetic fiber added to an active material of an electrode plate for a lead-acid battery.
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 electrode plates for lead-acid batteries has a thickness of 2 to 5 denier and a length of 0 to prevent the active material from falling off during the electrode plate manufacturing process, lead-acid battery assembly process, or lead-acid battery use. A synthetic fiber made of a copolymer of acrylic and vinyl chloride, for example, having an acid resistance of about .5 to 3 mm is mixed.
しかしながら、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性が劣下
する等極板製造工程上の問題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、効果が少なく、実用的でないものが多い。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 is a limit to increasing the amount added or increasing the length because there is a risk that it may cause problems in the equipolar plate manufacturing process due to poor filling of the paste into the grid substrate. be. Therefore, in recent years, attempts have been made to change the cross-sectional shape of synthetic fibers or to process the fibers into a wavy shape, but these efforts are often ineffective and impractical.
本発明は上記の如き点に鑑み、添加する合成繊維に多孔
性を保持せしめることで、繊維表面に均一に凹凸を形成
せしめて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。In view of the above points, the present invention aims to improve the adhesion with the active material by making the added synthetic fiber retain porosity, thereby forming unevenness uniformly on the fiber surface, thereby reducing the dropout of the active material. The purpose is to reduce the occurrence of defects in the electrode plate manufacturing process and lead-acid battery assembly process, and thereby extend the 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所定の太さを有する繊維
に加工、成形する。A raw material consisting of a polyolefin synthetic resin, a filler, and a plasticizer is heated and kneaded, and then processed and molded into fibers having a predetermined thickness.
然る後可塑剤あるいは可塑剤と充填剤とも適当な溶剤に
より溶出あるいは抽出して繊維に小孔を形成せしめる。
本発明に適用できる充填剤とは、多量の可塑剤を表面に
吸着保持するためのもので、シリカの微粉末やカーボン
ブラック等があげられる。さらには充填剤自体が容易に
溶出あるいは抽出されて、それらの逸出後が細孔となる
ような炭酸カルシウム、炭酸マグネシウム等のものでも
良い。このようにして得られた合成繊維は、表面に均一
なる凹凸が形成される。この繊維表面の小孔にはペース
ト練合時にペーストが進入するため活物質と繊維との密
着性が著しく優れたものになる。形成される細孔の大き
さ、量および繊維の強度は、充填剤の粒子径や可塑剤の
割合を変えることにより変えることができる。Thereafter, the plasticizer or both the plasticizer and the filler are eluted or extracted with a suitable solvent to form small pores in the fibers.
The filler applicable to the present invention is one for adsorbing and retaining a large amount of plasticizer on the surface, and includes fine silica powder, carbon black, and the like. Furthermore, fillers such as calcium carbonate, magnesium carbonate, etc., which are easily eluted or extracted and form pores after their escape, may also be used. The synthetic fiber thus obtained has uniform irregularities formed on its surface. Since the paste enters into the small pores on the fiber surface during paste kneading, the adhesion between the active material and the fibers becomes extremely excellent. The size and amount of pores formed and the strength of the fibers can be changed by changing the particle size of the filler and the proportion of the plasticizer.
実際には約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
ミクロン程度のものが多いので、理想的には1ミクロン
以上あつた方が活物質との密着性は良好である。また活
物質との密着性を向上させようとして充填剤の量を多く
すると繊維の強度は脆化、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が低下するため給
合的に3成分の最適な配合割合の範囲は、樹脂/充填剤
/可塑剤=15〜3V8〜17/58〜75(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%)とシリカ粉末(平均粒子径1.5μ
、15重量%)と可塑剤ジオクチルフタレート(D,O
,P)(60重量%)をミキサーで混合して原材料とし
た。In practice, size ranges of about 10 microns or less are possible, but the lead powder particles currently in use range from 0.5 to 1.
Since most of the particles are on the order of microns, ideally, the adhesiveness with the active material is better when the thickness is 1 micron or more. Furthermore, if the amount of filler is increased to improve the adhesion with the active material, the strength of the fibers becomes brittle, and if the amount of resin is increased to increase the strength of the fibers, the adhesion with the active material decreases. Overall, the optimum blending ratio of the three components is resin/filler/plasticizer=15-3V8-17/58-75 (all weight %). Example 1 Pellet-shaped low-density polyethylene (25% by weight) and silica powder (average particle size 1.5 μm)
, 15% by weight) and the plasticizer dioctyl phthalate (D,O
, P) (60% by weight) were mixed in a mixer to prepare a raw material.
この原材料を200±1(代)にて加熱混練した後押出
成形して、太さ約3デニールの長繊維を得た。しかる後
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、繊維に多孔性を持たせた。このようにして得ら
れた合成樹脂を約1ミリの長さに裁断した。これを鉛粉
に対して0.0鍾量%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%)とカーボンブラック(5重量%)、シリカ
粉末(1喧量%)およびペテロリウムオイル(6踵量%
)とをミキサーで混合し原材料とした。This raw material was heated and kneaded at 200±1 (generations) and then extruded to obtain long fibers having a thickness of about 3 deniers. Thereafter, the plasticizer in the fibers was extracted by ultrasonication in a trichlorethylene solution to make the fibers porous. The synthetic resin thus obtained was cut into lengths of approximately 1 mm. 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 substrate to obtain an electrode plate. Example 2 Pellet-shaped low-density polyethylene (
25% by weight), carbon black (5% by weight), silica powder (1% by weight) and petroleum oil (6% by weight).
) was mixed with a mixer to obtain a raw material.
しかる後実施例1と同様方法により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5h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。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 amount of active material that fell off when the chemically formed anode plate obtained according to the present invention was dropped from a height of 5 hours onto an iron plate alternately on the front and back sides is as shown in the drawing.
図面によつても明らかな如く、本発明による多孔性繊維
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。As is clear from the drawings, it can be seen that in the electrode plate to which the porous fibers according to the present invention were added, the active material did not fall off much, 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多孔性
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 porous synthetic fibers added to the electrode plate according to the present invention shown in the drawings 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。In the drawings, A represents a conventional electrode plate, and B represents an electrode plate according to the present invention.
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。As described above, according to the present invention, defects caused by falling off of active material from electrode plates in the manufacturing process of storage batteries are significantly reduced, and
No short circuit occurs at the bottom of the electrode plate group due to fallen active material.
It has great industrial value, such as improving the life performance of storage batteries.
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
0(1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.
It is a comparative diagram showing the amount of active material falling off when dropped from a height of 0 (1). A is a conventional electrode plate, and B is an electrode plate according to the present invention.
Claims (1)
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
維状に成型後可塑剤あるいは可塑剤と充填剤とを溶出あ
るいは抽出して多孔性を保持せしめ、多孔性を有する繊
維を所定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 a polyolefin synthetic resin, a filler, and a plasticizer are heated and kneaded, then formed into a fiber having a predetermined thickness, and then the plasticizer or the plasticizer and filler are eluted or extracted to maintain porosity. 1. A method for producing an electrode plate for a lead-acid battery, which comprises cutting porous fibers into a predetermined length and adding the cut fibers to a paste.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55056484A JPS6054741B2 (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 |
|---|---|---|---|
| JP55056484A JPS6054741B2 (en) | 1980-04-28 | 1980-04-28 | Manufacturing method of electrode plates for lead-acid batteries |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56152164A JPS56152164A (en) | 1981-11-25 |
| JPS6054741B2 true JPS6054741B2 (en) | 1985-12-02 |
Family
ID=13028370
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55056484A Expired JPS6054741B2 (en) | 1980-04-28 | 1980-04-28 | Manufacturing method of electrode plates for lead-acid batteries |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6054741B2 (en) |
-
1980
- 1980-04-28 JP JP55056484A patent/JPS6054741B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56152164A (en) | 1981-11-25 |
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