JP3568356B2 - Method of manufacturing prismatic battery and prismatic battery - Google Patents
Method of manufacturing prismatic battery and prismatic battery Download PDFInfo
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- JP3568356B2 JP3568356B2 JP11097197A JP11097197A JP3568356B2 JP 3568356 B2 JP3568356 B2 JP 3568356B2 JP 11097197 A JP11097197 A JP 11097197A JP 11097197 A JP11097197 A JP 11097197A JP 3568356 B2 JP3568356 B2 JP 3568356B2
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- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 34
- 239000002184 metal Substances 0.000 claims description 34
- 238000007747 plating Methods 0.000 claims description 20
- 239000011148 porous material Substances 0.000 claims description 16
- 239000011149 active material Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 239000007769 metal material Substances 0.000 claims description 5
- 238000010030 laminating Methods 0.000 claims description 2
- 235000021384 green leafy vegetables Nutrition 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- 238000003860 storage Methods 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 229910045601 alloy Inorganic materials 0.000 description 8
- 239000000956 alloy Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 6
- 238000007789 sealing Methods 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
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- 239000000203 mixture Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- BFDHFSHZJLFAMC-UHFFFAOYSA-L nickel(ii) hydroxide Chemical compound [OH-].[OH-].[Ni+2] BFDHFSHZJLFAMC-UHFFFAOYSA-L 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
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- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
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- 229910052779 Neodymium Inorganic materials 0.000 description 1
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- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
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- 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
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
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- Cell Electrode Carriers And Collectors (AREA)
- Secondary Cells (AREA)
- Battery Electrode And Active Subsutance (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、角形電池の製造方法と、極板を内蔵する角形電池に関する。
【0002】
【従来の技術】
スポンジ状金属多孔体は、孔径を100μmから数mm程度と自由に変更できる。このため、水酸化ニッケル粉末、水素吸蔵合金粉末等の様々な電極活物質に対して、それぞれの活物質の特性に合わせた最適な孔径を選んで電極とすることができ、また活物質の保持性も良いため、電池用極板として好ましい物性を備えている。
【0003】
スポンジ状金属多孔体は、スポンジ状の有機多孔体、すなわち、プラスチックフォームをメッキした後、ばい焼して有機多孔体を除去し、その後焼結して製作される。この方法で極板を製造する技術は、たとえば、特開平4−303564号公報に記載される。この公報に記載される方法は、下記の工程で極板を製造する。
【0004】
(1) ウレタンフォーム等のスポンジ状有機多孔体が、前処理された後、メッキ槽に浸漬されてメッキされる。このメッキ工程において、有機多孔体は、一定方向にテンションがかけられてメッキ槽に浸漬してメッキされる。この状態でメッキされた有機多孔体は、孔をテンション方向に引き伸ばした状態となる。
【0005】
(2) メッキした有機多孔体が、空気中でばい焼される。ばい焼されると、有機多孔体を構成している樹脂成分が除去される。樹脂成分が除去されると、メッキ部分が残る。
【0006】
(3) 樹脂成分を除去されたメッキ部が焼結されて金属多孔体となる。金属多孔体は、スポンジ状の有機多孔体の多孔質な微細な孔の内面に金属をメッキして焼結したものであるから、有機多孔体に近似する多孔質状態となる。
【0007】
(4) 金属多孔体を長方形に裁断する。裁断方向は、メッキ処理時のテンション方向が極板の長辺方向となるように裁断される。いいかえると、極板の長辺方向が、メッキ処理のテンション方向となるようにして極板を製造する。
【0008】
【発明が解決しようとする課題】
以上の工程で製造された極板は、有機多孔体をメッキする工程で、図1の矢印で示す方向にテンションをかけて製造されるので、金属多孔体1の孔2が図に示すように、極板3の長辺方向に引き伸ばされた形状となる。この方向に引き伸ばしてメッキして製造された金属多孔体1は、図の鎖線で示す方向にヒビやクラックが発生して強度が低下する欠点がある。矢印で示す方向に長い空隙ができるからである。金属多孔体1の強度低下は、電池組立時の歩留を低下させる。
【0009】
とくに、角形電池は、+−の電極を渦巻状に巻いて円筒外装缶に挿入する電池に比較して、極板の長辺方向の強度が低下すると、外装缶に挿入する工程で歩留が低下する。+−の極板を渦巻状に巻いて円筒外装缶に挿入する電池は、外側に巻かれた極板で内側の極板を押圧状態に保護しながら外装缶に挿入できる。しかしながら、+−の極板を単に積層して外装缶に挿入する角形電池は、外側の極板で内側の極板を押圧状態に保護して外装缶に挿入できない。このため、外装缶に挿入するときに、極板に挿入方向、すなわち、極板の長辺方向に力がかかる。このため、長辺方向に十分な強度のない極板は、外装缶に挿入する工程での、歩留を低下させる。とくに、長辺方向の強度が十分でなく、図3の鎖線で示す方向にヒビやクラックの発生しやすい極板は、外装缶に挿入されるときに、図2の拡大断面図に示すように、極板3がセパレータ4を突き破って内部ショートの原因となる。金属多孔体1が、ヒビやクラックで損傷を受けて、矢印Aで示す方向に外装缶に押し込まれると、極板3の表面が局部的に突出して、矢印Bで示すように、セパレータ4を突き破って内部ショートの原因となる。セパレータ4は極めて薄いので、金属多孔体1が極めて微細な領域で破損されても、これがセパレータ4を突き破って内部ショートの原因となる。
【0010】
さらに、角形電池の極板は、図3に示すように、長辺側の一端に電極リード5を接続して外装缶に挿入される。ここに電極リード5を接続している極板3に、鎖線で示す方向にクラックができると、電極リード5と極板3先端との電気抵抗が大きくなり、あるいは、極板3先端を電極リード5に電気接続できなくなって、極板3の実質容量を小さくして電池性能が低下する。
【0011】
さらに、以上の欠点は、極板3の金属多孔体1に充填する活物質量を多くして電池容量を大きくするほど顕著になる。それは、金属多孔体1の空隙率が大きくなって、金属多孔体1の強度が低下するからである。このため、大容量にするほど、前述の弊害が甚だしくなり、大容量の電池になるほど歩留が低下する欠点がある。
【0012】
本発明は、このような欠点を解決することを目的に開発されたものである。本発明の重要な目的は、大容量に設計できる極板を、高い歩留で角形外装缶に挿入できる角形電池と、この極板を使用した角形電池を提供することにある。
【0013】
【課題を解決するための手段】
本発明の請求項1の角形電池の製造方法は、ウレタンフォーム等の有機多孔体に、一定方向にテンションをかけながらメッキ処理する第1工程と、この工程に次いで加熱して有機多孔体を除去して金属多孔体1を作製する第2工程と、金属多孔体1に活物質を充填する第3工程と、活物質の充填された金属多孔体1を、角形電池の外装缶6に挿入できる長方形に裁断する第4工程と、長方形の極板3を積層した電極群7を、両側に配設する極板を角形外装缶6の内面に電気的に接触させる状態で挿入する工程からなる。
【0014】
さらに、本発明の角形電池の製造方法は、メッキ処理する第1工程において、有機多孔体のテンション方向を、長方形の極板3の短辺方向とすることを特徴とする。図4の矢印Aで示す方向に、有機多孔体にテンションをかけてメッキして製造された極板3は、矢印Bで示す方向の強度を強くできる。矢印Bで示す方向は、極板3を角型外装缶6に挿入する方向である。このため、この方向に強い極板3は、高い歩留で角型外装缶6に挿入できる。
【0015】
本発明の請求項2の角形電池は、一定方向に引っ張られながらメッキ処理された有機多孔体を、空気中でばい焼して金属多孔体1としており、この金属多孔体1の多孔質な空隙に活物質を充填して、角形電池の外装缶6に挿入できる長方形に裁断されてなる極板3を外装缶6に挿入している。この角形電池は、金属多孔体1を、有機多孔体を長方形の極板3の短辺方向に引っ張ってメッキ処理して製作している。さらに、長方形の極板3を積層した電極群7は、両側に配設する極板を角形外装缶6の内面に電気的に接触させる状態で外装缶6に挿入している。
【0016】
さらに、本発明の請求項3の角形電池は、有機多孔体をメッキするときのテンションの方向を特定して、極板3を構成する金属多孔体1の多孔質な孔2の平均的な内径を、極板3の長辺方向よりも短辺方向を長くしている。この角型電池も、長方形の極板3を積層した電極群7は、両側に配設する極板を角形外装缶6の内面に電気的に接触させる状態で外装缶6に挿入している。
【0017】
【発明の実施の形態】
以下、本発明の実施例を図面に基づいて説明する。ただし、以下に示す実施例は、本発明の技術思想を具体化するための製造方法と角形電池を例示するものであって、本発明は製造方法と角形電池を下記に特定しない。
【0018】
さらに、この明細書は、特許請求の範囲を理解し易いように、実施例に示される部材に対応する番号を、「特許請求の範囲の欄」、および「課題を解決するための手段の欄」に示される部材に付記している。ただ、特許請求の範囲に示される部材を、実施例の部材に特定するものでは決してない。
【0019】
図5に示す角形電池は、角型アルカリ蓄電池である。この角形アルカリ蓄電池は、ニッケル−水素蓄電池で、角形の外装缶6に電極群7を収納している。電極群7は、正極板3Aと負極板3Bとをセパレータ4を介して積層したものである。電極群7は、両側に配設する負極板3Bを角形外装缶6の内面に電気的に接触させている。電極群7の正極板3Aは、電極リード5を介して、外装缶6に絶縁して固定された封口蓋8の正極端子9に接続される。封口蓋8の正極端子9は安全弁を内蔵している。
【0020】
角形の外装缶6は鉄製であり、その表面にニッケルメッキを施してある。但し、外装缶は材質を鉄に特定せず、例えばステンレス製とすることも出来るのは言うまでもない。
【0021】
ニッケル−水素蓄電池である角形電池は、外装缶6に、電極群7を挿入し、電解液を注入して、外装缶6の開口部に封口蓋8をレーザー溶接して製造される。正極板と負極板とは下記のようにして製造される。
【0022】
A 正極板の製造
(1) 下記の工程で金属多孔体を作製する。
連続気泡のポリウレタンフォームであるスポンジ状の有機多孔体を、前処理した後、一定の方向にテンションをかけた状態、すなわち、多少引き伸ばした状態で、電解槽のメッキ液に浸漬してメッキする。有機多孔体を引っ張るテンションは、有機多孔体の厚さと幅を考慮して最適値に設定する。たとえば、厚さを約2mm、幅を500mmとする有機多孔体を、金属多孔体の多孔質な孔の長径/短径の比を約1.3とするテンションで引っ張りながらメッキする。メッキした有機多孔体を、750℃の温度で所定時間ばい焼して、有機多孔体の樹脂成分を除去し、さらに、還元雰囲気で焼結して金属多孔体を製作する。この工程で製作されたスポンジ状の金属多孔体は、引き延ばされた方向に対して垂直な方向が平行な方向よりも機械的強度が強くなる。
【0023】
(2) 下記のものを混練りして、活物質ペーストとする。
水酸化ニッケル粉末…………………………………………90重量部
(2.5wt%の亜鉛と、1wt%のコバルトを共沈成分として含有)
コバルト粉末……………………………………………………7重量部
酸化亜鉛粉末……………………………………………………3重量部
ヒドロキシプロピルセルロース0.2重量%水溶液……50重量部
【0024】
(3) 作製した活物質ペーストを、金属多孔体の空隙に充填し、乾燥後にプレスして厚みを調整し、放電容量が600mAhとなる長方形に裁断して、図4に示すように、短辺に電極リード5を電気接続する。長方形の正極板は、メッキ処理するときに有機多孔体を引っ張る方向が長方形の短辺方向となる形状に裁断される。いいかえると、メッキ処理するときに有機多孔体を引っ張るテンション方向を、長方形に裁断される正極板の短辺方向とする。この工程で製作された正極板は、図4の要部拡大図に示すように、スポンジ状金属多孔体1の多孔質な孔2の平均的な内径が、極板3の長辺方向よりも短辺方向に長くなっている。
【0025】
B 負極板の製造
(1) 水素吸蔵合金の作製と粉砕
ミッシュメタル(La、Ce、Nd、Pr等の希土類元素の混合物)と、コバルトと、アルミニウムと、マンガンとを所定の重量に秤量して混合し、これをルツボに入れて高周波溶解炉で溶融した後冷却し、下記の組成式の水素吸蔵合金電極を作製する。
MmNi3.4Co0.8Al0.2Mn0.6
そして、得られた水素吸蔵合金の鋳塊を、不活性ガス中で平均粒径が150μmとなるように粉砕する。
【0026】
(2) 水素吸蔵合金ペーストの作製
粉砕した水素吸蔵合金の粉末に、結着剤としてポリエチレンオキサイド粉末を添加し、さらにイオン交換水を添加、混練してペースト状のスラリーとする。結着剤であるポリエチレンオキサイド粉末の添加量は、水素吸蔵合金に対して0.5重量%とする。
【0027】
(3) 水素吸蔵合金のスラリーを集電体に塗着、乾燥する
得られたスラリーを、パンチングメタルからなる集電体の両面に、一定の厚さにコーティングして塗着した後、乾燥し、プレスを行い、厚みを調整する。その後、所定サイズに裁断して負極板とする。なお、集電体として、スポンジ状の金属多孔体、ニッケル繊維マット等を用いることも可能であり、この場合には、これら集電体に活物質ペーストを充填して作製する。
【0028】
次いで、図5に示すように、正極板3Aと負極板3Bとの間にセパレータ4を介在させて絶縁し、これらを積層して電極群7を構成する。セパレータ4には、厚みを0.2mmとするポリプロピレン製の不織布を使用する。電極群7は放電容量を600mAhとなるようにする。電極群7を角形の外装缶6に挿入し、1.25gの電解液を注入して、外装缶6の開口部を封口蓋8で閉塞する。電解液には、LiOH、NaOHを含有する7〜8.5NのKOH水溶液を使用する。
【0029】
【発明の効果】
本発明の角形電池の製造方法と角形電池は、活物質の充填量を多くして、大容量に設計できる極板を、高い歩留で角形外装缶に挿入できる特長がある。それは、本発明の方法で製造された極板の金属多孔体が、長方形の長辺方向の強度が強くなって、外装缶に確実に挿入できるからである。長方形の長辺方向に十分な強度のある金属多孔体は、角形電池の外装缶に高い歩留で挿入できる。それは、従来の極板のように、図2に示すごとく、極板の局部に発生するヒビやクラックが、セパレータを突き破って内部ショートの原因となることがないからである。また、長辺方向に十分な強度の極板は、角形電池の外装缶に押し込まれるときに、変形等の形状変化もせずに、確実に外装缶に挿入される。とくに、有機多孔体の空隙率を高くして、空隙に多量の外装缶を充填する極板は、強度が低下する傾向があるが、本発明の方法で製造された極板は、長辺方向に十分な強度があって、小型の外装缶に確実に挿入できる特長がある。
【図面の簡単な説明】
【図1】従来の角形電池に使用する極板の一部拡大正面図
【図2】図1に示す極板を外装缶に挿入する状態を示す拡大断面図
【図3】電極リードを接続している従来の極板の正面図
【図4】本発明の実施例の角形電池に使用する極板の一部拡大正面図
【図5】本発明の実施例の角形電池の一部断面斜視図
【符号の説明】
1…金属多孔体
2…孔
3…極板 3A…正極板 3B…負極板
4…セパレータ
5…電極リード
6…外装缶
7…電極群
8…封口蓋
9…正極端子[0001]
TECHNICAL FIELD OF THE INVENTION
The present invention includes a method for manufacturing a prismatic battery, relates prismatic battery with a built-in electrode plates.
[0002]
[Prior art]
The pore size of the sponge-like porous metal body can be freely changed from 100 μm to several mm. For this reason, for various electrode active materials such as nickel hydroxide powder and hydrogen storage alloy powder, it is possible to select an optimal pore size according to the characteristics of each active material and use it as an electrode. It has good physical properties, and thus has preferable physical properties as a battery electrode plate.
[0003]
The sponge-like porous metal body is manufactured by plating a sponge-like organic porous body, that is, a plastic foam, removing the organic porous body by roasting, and then sintering. A technique for manufacturing an electrode plate by this method is described in, for example, JP-A-4-303564. The method described in this publication produces an electrode plate in the following steps.
[0004]
(1) A sponge-like organic porous material such as urethane foam is immersed in a plating tank and plated after pre-treatment. In this plating step, the organic porous material is plated by being immersed in a plating tank under tension in a certain direction. The organic porous body plated in this state is in a state where the holes are elongated in the tension direction.
[0005]
(2) The plated organic porous body is roasted in the air. After roasting, the resin component constituting the organic porous material is removed. When the resin component is removed, a plated portion remains.
[0006]
(3) The plated portion from which the resin component has been removed is sintered to form a porous metal body. Since the porous metal body is formed by plating a metal on the inner surface of the porous fine pores of the sponge-like organic porous body and sintering the metal, the porous state becomes a porous state similar to the organic porous body.
[0007]
(4) The metal porous body is cut into a rectangle. The cutting direction is such that the tension direction during the plating process is the long side direction of the electrode plate. In other words, the electrode plate is manufactured such that the long side direction of the electrode plate becomes the tension direction of the plating process.
[0008]
[Problems to be solved by the invention]
The electrode plate manufactured in the above steps is manufactured by applying tension in the direction shown by the arrow in FIG. 1 in the step of plating the organic porous body, so that the
[0009]
In particular, in the case of a prismatic battery, when the strength in the long side direction of the electrode plate is reduced as compared with a battery in which the positive and negative electrodes are spirally wound and inserted into a cylindrical outer can, the yield in the step of inserting the outer can is reduced. descend. The battery in which the positive and negative electrode plates are spirally wound and inserted into the cylindrical outer can can be inserted into the outer can while protecting the inner electrode plate in a pressed state with the outer electrode plate. However, in the case of a prismatic battery in which positive and negative electrode plates are simply laminated and inserted into an outer can, the outer electrode plate protects the inner electrode plate in a pressed state and cannot be inserted into the outer can. For this reason, when inserting into an exterior can, a force is applied to the electrode plate in the insertion direction, that is, in the long side direction of the electrode plate. For this reason, an electrode plate having insufficient strength in the long side direction lowers the yield in the step of inserting it into the outer can. In particular, the strength of the long-side direction is not sufficient, prone plate of cracks and cracks in the direction indicated by the chain line in FIG. 3, when inserted into the outer can, as shown in the enlarged cross-sectional view of FIG. 2 In addition, the
[0010]
Further, as shown in FIG. 3, the electrode plate of the prismatic battery is connected to the
[0011]
Further, the above disadvantages become more remarkable as the amount of active material filled in the
[0012]
The present invention has been developed to solve such disadvantages. An important object of the present invention is to provide a plate that can be designed large, the prismatic battery that can be inserted into prismatic outer can with a high yield, a prismatic battery using this electrode plate.
[0013]
[Means for Solving the Problems]
Method for manufacturing a prismatic batteries according to
[0014]
Furthermore, the manufacturing method of rectangular batteries of the present invention, in the first step of plating treatment, the tension direction of the organic porous material, characterized by a short side direction of the
[0015]
In the prismatic battery according to the second aspect of the present invention, the organic porous body that has been plated while being pulled in a certain direction is roasted in the air to form a
[0016]
Further, in the prismatic battery according to
[0017]
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, embodiments of the present invention will be described with reference to the drawings. However, the following examples illustrate a manufacturing method and a prismatic battery for embodying the technical idea of the present invention, and the present invention does not specify the manufacturing method and the prismatic battery below.
[0018]
Further, in this specification, in order to make it easy to understand the claims, the numbers corresponding to the members shown in the embodiments are referred to as "claims" and "means for solving the problem". Are added to the members indicated by "." However, the members described in the claims are not limited to the members of the embodiments.
[0019]
The prismatic battery shown in FIG. 5 is a prismatic alkaline storage battery. This prismatic alkaline storage battery is a nickel-hydrogen storage battery, in which an electrode group 7 is housed in a prismatic
[0020]
The rectangular outer can 6 is made of iron, and its surface is plated with nickel. However, it goes without saying that the outer can is not limited to iron and may be made of, for example, stainless steel.
[0021]
A prismatic battery, which is a nickel-hydrogen storage battery, is manufactured by inserting an electrode group 7 into an
[0022]
A. Manufacture of positive electrode plate
(1) A porous metal body is prepared in the following steps.
After pretreatment, the sponge-like organic porous body, which is an open-celled polyurethane foam, is immersed in a plating solution in an electrolytic cell and plated in a state where tension is applied in a certain direction, that is, in a slightly stretched state. The tension for pulling the organic porous body is set to an optimum value in consideration of the thickness and width of the organic porous body. For example, an organic porous body having a thickness of about 2 mm and a width of 500 mm is plated while being pulled by a tension that makes the ratio of the major axis / minor axis of the porous hole of the metallic porous body about 1.3. The plated organic porous body is roasted at a temperature of 750 ° C. for a predetermined time to remove the resin component of the organic porous body, and then sintered in a reducing atmosphere to produce a metal porous body. In the sponge-like porous metal body manufactured in this step, the mechanical strength is higher in a direction perpendicular to the stretching direction than in a direction parallel to the stretching direction.
[0023]
(2) The following are kneaded to form an active material paste.
Nickel hydroxide powder 90 parts by weight (containing 2.5 wt% of zinc and 1 wt% of cobalt as a coprecipitating component)
Cobalt powder 7 parts by weight of
(3) The prepared active material paste was filled in the voids of the porous metal body, dried, pressed to adjust the thickness, cut into a rectangle having a discharge capacity of 600 mAh, and then cut into short sides as shown in FIG. Is electrically connected to the
[0025]
B Production of negative electrode plate
(1) Preparation of hydrogen storage alloy, crushed misch metal (a mixture of rare earth elements such as La, Ce, Nd, Pr), cobalt, aluminum, and manganese are weighed to a predetermined weight and mixed. It is put in a crucible, melted in a high-frequency melting furnace and then cooled to produce a hydrogen storage alloy electrode having the following composition formula.
MmNi3.4Co0.8Al0.2Mn0.6
Then, the obtained ingot of the hydrogen storage alloy is pulverized in an inert gas so that the average particle size becomes 150 μm.
[0026]
(2) Preparation of hydrogen storage alloy paste Polyethylene oxide powder as a binder is added to the pulverized hydrogen storage alloy powder, and ion-exchanged water is further added and kneaded to form a paste slurry. The added amount of the polyethylene oxide powder as the binder is 0.5% by weight based on the hydrogen storage alloy.
[0027]
(3) A slurry of the hydrogen storage alloy is applied to the current collector and dried.The obtained slurry is coated on both sides of a current collector made of punched metal to a predetermined thickness, applied, and then dried. Press and adjust the thickness. Then, it is cut to a predetermined size to obtain a negative electrode plate. Note that a sponge-like porous metal material, a nickel fiber mat, or the like can be used as the current collector. In this case, the current collector is filled with an active material paste and manufactured.
[0028]
Next, as shown in FIG. 5, a
[0029]
【The invention's effect】
The prismatic battery manufacturing method and prismatic battery according to the present invention have a feature that an electrode plate that can be designed to have a large capacity by increasing the filling amount of an active material can be inserted into a prismatic outer can at a high yield. This is because the strength of the porous metal body of the electrode plate manufactured by the method of the present invention in the long side direction of the rectangle is increased and the porous metal body can be reliably inserted into the outer can. The porous metal body having sufficient strength in the long side direction of the rectangle can be inserted into the outer can of the prismatic battery at a high yield. This is because, unlike the conventional electrode plate, as shown in FIG. 2, cracks or cracks generated locally in the electrode plate do not break through the separator and cause an internal short circuit. Further, when the electrode plate having sufficient strength in the long side direction is pushed into the outer can of the prismatic battery, the electrode plate is surely inserted into the outer can without deformation such as deformation. In particular, the porosity of the organic porous material is increased, and the electrode plate in which a large amount of the outer can is filled in the void tends to have a reduced strength.However, the electrode plate manufactured by the method of the present invention has It has the strength that it can be inserted securely into a small outer can.
[Brief description of the drawings]
FIG. 1 is a partially enlarged front view of an electrode plate used in a conventional prismatic battery. FIG. 2 is an enlarged sectional view showing a state in which the electrode plate shown in FIG. 1 is inserted into an outer can. FIG. FIG. 4 is a partially enlarged front view of an electrode plate used in a prismatic battery according to an embodiment of the present invention. FIG. 5 is a partial cross-sectional perspective view of a prismatic battery according to an embodiment of the present invention. [Explanation of symbols]
DESCRIPTION OF
Claims (3)
メッキ処理する第1工程において、有機多孔体のテンション方向を、長方形の極板(3)の短辺方向とすることを特徴とする角形電池の製造方法。 A first step of plating while applying tension to the organic porous body in a certain direction, and a second step of heating and removing the organic porous body to produce a porous metal body (1) following this step; a third step of filling an active material into the body (1), filled porous metal body of active material (1), cut into rectangles can be inserted into the outer can (6) of the prismatic battery, a rectangular plate ( a fourth step of a 3), a rectangular plate (3) laminated electrode group (7), the electrode plate arranged on both sides on the inner surface of the prismatic outer can (6) in a state electrically contacting in manufacturing method of prismatic battery comprising a step of inserting,
A method for manufacturing a prismatic battery, wherein in the first step of plating, the tension direction of the organic porous material is set to the short side direction of the rectangular electrode plate (3) .
金属多孔体(1)が、有機多孔体を長方形の極板(3)の短辺方向に引っ張ってメッキ処理されて製作されてなり、かつ、前記長方形の極板 (3) を積層した電極群 (7) が、両側に配設する極板を角形外装缶 (6) の内面に電気的に接触させる状態で外装缶 (6) に挿入してなることを特徴とする角形電池。The organic porous material that has been plated while being pulled in a certain direction is roasted in air to form a porous metal material (1), and the porous material of the porous metal material (1) is filled with an active material. Then, in a rectangular battery obtained by inserting an outer can (6) into a rectangular plate that can be inserted into an outer can (6) of a prismatic battery (3),
Electrode metal porous body (1) is Ri Na is manufactured by plating process by pulling the organic porous body in the short side direction of the rectangular plate (3), and, by laminating the plates (3) of the rectangular A prismatic battery wherein the group (7) is inserted into the outer can (6) in a state where the electrode plates provided on both sides are in electrical contact with the inner surface of the rectangular outer can (6) .
極板(3)を構成する金属多孔体(1)の多孔質な孔(2)の平均的な内径が、極板(3)の長辺方向よりも短辺方向を長くしてなり、かつ、前記長方形の極板 (3) を積層した電極群 (7) が、両側に配設する極板を角形外装缶 (6) の内面に電気的に接触させる状態で外装缶 (6) に挿入してなることを特徴とする角形電池。The organic porous material that has been plated while being pulled in a certain direction is roasted in air to form a porous metal material (1), and the porous material of the porous metal material (1) is filled with an active material. Then, in a prismatic battery obtained by inserting an electrode plate (3) cut into a rectangular shape that can be inserted into an outer can (6) of a prismatic battery into an outer can (6),
Average inner diameter of the porous pores of the porous metallic body forming the electrode plate (3) (1) (2), the electrode plate (3) Ri greens by increasing the short-side direction than the longitudinal direction of, and said rectangular plate (3) laminated electrode group is (7), in a state in which electrical contact with the inner surface of the plate to be arranged on both sides prismatic outer can (6) to the outer can (6) A prismatic battery characterized by being inserted .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11097197A JP3568356B2 (en) | 1997-04-28 | 1997-04-28 | Method of manufacturing prismatic battery and prismatic battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11097197A JP3568356B2 (en) | 1997-04-28 | 1997-04-28 | Method of manufacturing prismatic battery and prismatic battery |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH10302781A JPH10302781A (en) | 1998-11-13 |
| JP3568356B2 true JP3568356B2 (en) | 2004-09-22 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP11097197A Expired - Fee Related JP3568356B2 (en) | 1997-04-28 | 1997-04-28 | Method of manufacturing prismatic battery and prismatic battery |
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| JP4644336B2 (en) * | 2000-05-10 | 2011-03-02 | パナソニック株式会社 | Method for producing positive electrode for alkaline storage battery |
| JPWO2012111699A1 (en) * | 2011-02-18 | 2014-07-07 | 住友電気工業株式会社 | Electrode using three-dimensional network aluminum porous body, non-aqueous electrolyte battery using the electrode, capacitor using non-aqueous electrolyte, and lithium ion capacitor |
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| JPH10302781A (en) | 1998-11-13 |
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