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JPH113701A - Manufacture of battery electrode and equipment thereof - Google Patents

Manufacture of battery electrode and equipment thereof

Info

Publication number
JPH113701A
JPH113701A JP9151097A JP15109797A JPH113701A JP H113701 A JPH113701 A JP H113701A JP 9151097 A JP9151097 A JP 9151097A JP 15109797 A JP15109797 A JP 15109797A JP H113701 A JPH113701 A JP H113701A
Authority
JP
Japan
Prior art keywords
laminate
roll
electrode
battery electrode
heated
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.)
Withdrawn
Application number
JP9151097A
Other languages
Japanese (ja)
Inventor
Kimihiro Morita
公裕 守田
Takahiro Yamamoto
高弘 山本
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.)
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry 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 Asahi Chemical Industry Co Ltd filed Critical Asahi Chemical Industry Co Ltd
Priority to JP9151097A priority Critical patent/JPH113701A/en
Publication of JPH113701A publication Critical patent/JPH113701A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • 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

  • Battery Electrode And Active Subsutance (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a battery electrode with high bulk density and a smooth surface through less pressing number and light pressing by preheating a laminate prepared by applying an electrode mix to one side or both sides of a metal foil current collector, before it is pressed or heat-roll pressed. SOLUTION: A laminate 7 is successively fed from a winding out roll 1, where the laminate 7 is wound and stacked, and sent to a preheating part 3 through a guide 2. The laminate 7 is passed on a plurality of small diameter heating drums or on a large diameter heating drum, having the dimension capable of entering the preheating part 3, heated once, then sent to a heat press roll 4, without the temperature is not being lowered much. The laminate 7 is heated and at the same time pressed with the heat press roll 4 comprising two heating rolls and a hydraulic cylinder 6. The heated and pressed laminate 7 is wound with a winding roll 5.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、電池用の電極作製
技術に関し、詳しくは積層捲回されてなる金属箔集電体
上に、電極合剤を塗布した積層体の密度を容易に向上さ
せる電池電極の製造方法及びその製造装置に関する。特
にリチウム電池、リチウムイオン二次電池に用いるもの
に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a technique for manufacturing an electrode for a battery, and more particularly to a technique for easily increasing the density of a laminate obtained by applying an electrode mixture onto a metal foil current collector formed by lamination. The present invention relates to a method for manufacturing a battery electrode and an apparatus for manufacturing the same. Particularly, the present invention relates to a battery used for a lithium battery and a lithium ion secondary battery.

【0002】[0002]

【従来の技術】従来、電池電極は金属箔集電体上に電極
合剤を塗布した後、室温で加圧プレスを行うことで嵩密
度を高めていた。この方法では、より高い嵩密度を得る
ためには、圧力を高め、さらにプレス回数を増やすため
に結果として無理なプレスが行われるため活物質の破壊
や集電体箔の破壊、また粒子の脱落等の問題が生じてい
た。そこで活物質間どうし、活物質と集電体間を結合さ
せる目的で添加したバインダーを加熱し流動化させた状
態で加圧することで嵩密度を高めること、すなわち加熱
ロールを用いた加熱ロールプレスが提案されている。
(特開平5ー129020号公報) しかしながら、加熱ロールプレスだけでは伝熱が不十分
であり、目的とする嵩密度を容易に得られていない。一
方、伝熱を充分にとるためにプレス速度を遅くするの
は、生産性が悪くなるという問題があった。
2. Description of the Related Art Conventionally, for a battery electrode, after applying an electrode mixture on a metal foil current collector, the bulk density has been increased by performing a pressure press at room temperature. In this method, in order to obtain a higher bulk density, the pressure is increased, and further pressing is performed. As a result, excessive pressing is performed, so that the active material is destroyed, the current collector foil is destroyed, and the particles fall off And other problems. Therefore, by increasing the bulk density by applying pressure while heating and fluidizing the binder added for the purpose of bonding between the active materials and between the active material and the current collector, that is, a heating roll press using a heating roll is used. Proposed.
However, heat transfer is not sufficient only by a heated roll press, and a desired bulk density cannot be easily obtained. On the other hand, if the pressing speed is reduced in order to obtain a sufficient heat transfer, there is a problem that productivity is deteriorated.

【0003】[0003]

【発明が解決しようとする課題】この発明は、この様な
問題点を解消するためになされたものであって、金属箔
集電体上に電極合剤を塗布した積層体を予備加熱した
後、加圧プレスを行うことであり、より好ましくはこの
加圧プレスが加熱ロールプレスであり、これを併用する
ことにより、少ないプレス回数、軽いプレス圧で嵩密度
の高い平滑な表面を有する電池電極を提供することを目
的とするものである。
SUMMARY OF THE INVENTION The present invention has been made in order to solve such a problem, and it is intended that a laminate obtained by applying an electrode mixture onto a metal foil current collector be preheated. , A pressure press, more preferably this pressure press is a heated roll press, by using this in combination, a small number of presses, a battery electrode having a high bulk density and a smooth surface with a light press pressure The purpose is to provide.

【0004】[0004]

【課題を解決するための手段】本発明の電池電極の製造
方法は、帯状の金属箔集電体に電極合剤を片面または両
面に塗布してなる、一般的な積層捲回されてなる電池に
おける、電池電極の製造方法であって、金属箔集電体お
よびその片面または両面に電極合剤を塗布した積層体を
プレスまたは加熱ロールプレスする前に予備加熱する事
を特徴とするものである。
A method of manufacturing a battery electrode according to the present invention is directed to a general laminated wound battery comprising an electrode mixture applied to one or both sides of a strip-shaped metal foil current collector. The method for producing a battery electrode according to any one of claims 1 to 3, characterized in that the metal foil current collector and a laminate obtained by applying the electrode mixture to one or both surfaces thereof are preheated before pressing or hot roll pressing. .

【0005】本発明の予備加熱装置としては、一般的な
加熱装置で良いが短時間で塗膜温度の昇温が可能で、さ
らにロールプレスの瞬間まで電極合剤の流動性を失わな
い程度に塗膜の温度を維持できる点から、予備加熱用恒
温層中に一つの大きなドラムか或いは小さいドラムを数
個配置する事が好ましい。予備加熱温度としては、電極
合剤の融点温度より50℃程度低くすることが好まし
い。
As the preheating device of the present invention, a general heating device may be used, but the temperature of the coating film can be raised in a short time, and the fluidity of the electrode mixture is not lost until the moment of roll pressing. From the viewpoint that the temperature of the coating film can be maintained, it is preferable to arrange one large drum or several small drums in the preheating constant temperature layer. The preheating temperature is preferably set to be lower by about 50 ° C. than the melting point of the electrode mixture.

【0006】このような構成により、少ないプレス回
数、軽いプレス圧で嵩密度の高い平滑な表面を有する電
池電極が得られる。本発明で用いる電極は、正極活物質
として下記の化学組成式(I)で示される酸化物が挙げ
られる。 化学組成式(I):Lixyz2 (Mは遷移金属の
少なくとも一種を表し、Nは非遷移金属の少なくとも一
種を表し、XYZ は各々0.05<X<1.10,0.8
5<Y≦1.00,0≦Z<0.10の数である。) 本発明の正極の活物質に好ましく用いられる酸化物とし
ては、化学組成式Li xyz2 (Mはコバルト、ニ
ッケル、マンガン及びその他の遷移金属の一種、または
それらの混合物を表し、NはAl、In、Snの少なく
とも一種を表し、XYZ は各々0.05<X<1.10,
0.85<Y≦1.00,0≦Z<0.10)である。
もっと好ましくはLiCoSnO2,LiNiSnz
2、LiNiSnzO2、LiMnSnz2及びこれら
の混合物である。(ただし、0≦Z<0.10であ
る。) 尚、上記の化学組成式で定義した無機化合物には、Li
0.5MnO2、すなわち一般にLiMn24と記述される
組成の化合物も含む。また、Z=0、すなわちAl,I
n、Snを含まない場合も本発明の範囲である。
[0006] With this configuration, the number of press times is small.
With a small pressing pressure, an electrode with a smooth surface with a high bulk density
A pond electrode is obtained. The electrode used in the present invention is a positive electrode active material.
Examples include oxides represented by the following chemical composition formula (I).
Can be Chemical composition formula (I): LixMyNzOTwo(M is the transition metal
N represents at least one of the non-transition metals
Represents the species,XYZAre 0.05 <X <1.10 and 0.8, respectively.
5 <Y ≦ 1.00, 0 ≦ Z <0.10. An oxide preferably used for the active material of the positive electrode of the present invention
The chemical composition formula Li xMyNzOTwo(M is cobalt, d
One of nickel, manganese and other transition metals, or
N represents less of Al, In and Sn.
Both represent a kind,XYZAre 0.05 <X <1.10.
0.85 <Y ≦ 1.00, 0 ≦ Z <0.10).
More preferably LiCoSnOTwo, LiNiSnz
OTwo, LiNiSnzOTwo, LiMnSnzOTwoAnd these
Is a mixture of (However, 0 ≦ Z <0.10
You. The inorganic compounds defined by the above chemical composition formula include Li
0.5MnOTwoIe, generally LiMnTwoOFourDescribed as
Also includes compounds of the composition. Z = 0, that is, Al, I
The case where n and Sn are not included is also within the scope of the present invention.

【0007】本発明の正極と組み合わされる負極の活物
質としては充放電が可能なものであれば特に制限される
ものではない。たとえば、特開昭62ー90863号公
報に記載の種々の炭素材料、真比重が1.3〜1.8g
/cm3の範囲にある各種の炭素材料、及び高結晶性の
炭素材料である天然及び人造の各種グラファイト等があ
げられる。例えばこのような炭素材料としてコークス、
アセチレンブラック、活性炭、ニードルコークス、メソ
フェーズマイクロビーズ、各種の炭素繊維、熱分解炭
素、フリュードコークスがあげられる。
[0007] The active material of the negative electrode combined with the positive electrode of the present invention is not particularly limited as long as it can be charged and discharged. For example, various carbon materials described in JP-A-62-90863, having a true specific gravity of 1.3 to 1.8 g
/ Cm 3 , and various types of highly crystalline carbon materials, such as natural and artificial graphites. For example, coke as such a carbon material,
Examples include acetylene black, activated carbon, needle coke, mesophase microbeads, various carbon fibers, pyrolytic carbon, and fluid coke.

【0008】本発明に関わる導電助剤の材質としては、
導電性が高ければ特に制限されるものではない。たとえ
ば炭素などは導電助剤としてよく添加される材料である
が、炭素の種類には特に制限はなく、活性炭、各種のコ
ークス、天然及び人造の黒鉛等を用いることができる。
これらの炭素のうち、その電気伝導性が良好であること
から天然及び人造の各種黒鉛類が好ましい。
[0008] The material of the conductive auxiliary agent according to the present invention includes:
There is no particular limitation as long as the conductivity is high. For example, carbon or the like is a material often added as a conductive additive, but the type of carbon is not particularly limited, and activated carbon, various cokes, natural and artificial graphite, and the like can be used.
Of these carbons, various natural and artificial graphites are preferred because of their good electrical conductivity.

【0009】本発明の導電助剤の形状には特に制限はな
いが、球形、破砕状のものが好ましい。本発明の電池電
極に用いる電極合剤は、特に制限はないが、正極・負極
に関わらず種々の方法により活物質と導電助剤を気体中
で混合した後に、結着剤を含む液体に分散することでス
ラリーを調製して作成される。その後、金属箔集電体上
に塗布・乾燥して積層体とする。ただし、負極について
は導電助剤を用いない場合もある。
The shape of the conductive additive of the present invention is not particularly limited, but is preferably spherical or crushed. The electrode mixture used for the battery electrode of the present invention is not particularly limited, but the active material and the conductive auxiliary are mixed in a gas by various methods regardless of the positive electrode or the negative electrode, and then dispersed in a liquid containing a binder. To prepare a slurry. After that, it is applied and dried on the metal foil current collector to form a laminate. However, a conductive auxiliary may not be used for the negative electrode in some cases.

【0010】スラリーを塗布する集電体にはアルミニウ
ムを正極に、銅を負極に用いるのが好ましい。結着剤と
してはテフロン、ポリエチレン、ニトリルゴム、ポリブ
タジエン、ブチルゴム、ポリスチレン、スチレン/ブタ
ジエンゴム、多硫化ゴム、ニトロセルロース、シアノエ
チルセルロース、各種のラテックス及びアクリロニトリ
ル、フッ化ビニル、フッ化ビニリデン、フッ化プロピレ
ン、フッ化クロロプレン等の重合体及びれらの混合体な
どが用いられる。中でもフッ化ビニリデン、フッ化プロ
ピレン、フッ化クロロプレン等の重合体が好ましい。加
圧プレスの温度は特に制限はないが、嵩密度を効率よく
あげるためには、使用しているバインダーの融点付近、
好ましくは融点+20℃〜融点−20℃の範囲、より好
ましくは融点−20℃の温度条件が好ましい。
It is preferable that aluminum is used for the positive electrode and copper is used for the negative electrode for the current collector to which the slurry is applied. Teflon, polyethylene, nitrile rubber, polybutadiene, butyl rubber, polystyrene, styrene / butadiene rubber, polysulfide rubber, nitrocellulose, cyanoethylcellulose, various latexes and acrylonitrile, vinyl fluoride, vinylidene fluoride, propylene fluoride And polymers such as chloroprene fluoride and mixtures thereof. Among them, polymers such as vinylidene fluoride, propylene fluoride, and chloroprene fluoride are preferred. The temperature of the pressure press is not particularly limited, but in order to increase the bulk density efficiently, around the melting point of the binder used,
The temperature is preferably in the range of melting point + 20 ° C. to melting point −20 ° C., more preferably in the range of melting point −20 ° C.

【0011】[0011]

【発明の実施の形態】以下、実施例、比較例により本発
明をさらに詳しく説明する。図1は加圧プレス機の一例
であり、図2は図1中の予備加熱部分の一例を示したも
のである。図2は、図1中の3、予備加熱部の内部の例
である。小径加熱ドラム8ならば複数個、大径加熱ドラ
ム9であれば予備加熱部に入る限りの大きさの径である
事が重要で、積層体が直接この加熱ドラムに接しながら
移動することより積層体の温度を短時間で目標温度まで
上昇させ、更に前記ドラム径及び個数とすることで、積
層体が加熱ドラムに接する時間を長くとれるため加熱プ
レスロール4に達するまでの温度低下を最小限に抑える
ことが可能である。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples. FIG. 1 shows an example of a press machine, and FIG. 2 shows an example of a preheating portion in FIG. FIG. 2 is an example of the inside of the preheating unit 3 in FIG. It is important for the small diameter heating drum 8 to have a plurality of diameters, and for the large diameter heating drum 9 to have a diameter large enough to enter the preheating section. By raising the temperature of the body to the target temperature in a short time and further setting the drum diameter and the number, the time required for the laminated body to come into contact with the heating drum can be lengthened, so that the temperature decrease before reaching the heating press roll 4 is minimized. It is possible to suppress.

【0012】図1に示すように、積層体7が捲回積層さ
れた巻出しロール1から積層体7が順次送り出され、ガ
イド2を介して予備加熱部3に送られる。予備加熱部3
内ではドラム8上を積層体7が通るようになされてお
り、積層体7は一端昇温され、その後温度低下の少ない
まま加熱プレスロール4に送られる。加熱プレスロール
4は二つの加熱ロールと、油圧シリンダ6からなり、送
られた積層体7は加熱ロール4に挟まれ、加熱されなが
ら油圧シリンダ6により加圧される。加熱加圧された積
層体7は、その後巻取り手段5(ロール)により巻き取
られる。
As shown in FIG. 1, the laminate 7 is sequentially sent out from the unwinding roll 1 on which the laminate 7 is wound and laminated, and sent to the preheating unit 3 via the guide 2. Preheating unit 3
Inside, the laminated body 7 passes over the drum 8, the temperature of the laminated body 7 is raised once, and thereafter, the laminated body 7 is sent to the heating press roll 4 with a small temperature decrease. The heating press roll 4 includes two heating rolls and a hydraulic cylinder 6. The fed laminate 7 is sandwiched between the heating rolls 4, and is pressed by the hydraulic cylinder 6 while being heated. The heat-pressed laminate 7 is then wound by winding means 5 (roll).

【0013】このようにして形成された積層体7は、少
ないプレス回数、軽いプレス圧で嵩密度の高い平滑な表
面を有する電池電極となる。本発明はこれらの装置に制
限されるものではなく、予備加熱部分から加熱プレスロ
ールにいたるまでの温度低下が小さければ小さいほど良
い。
The laminate 7 thus formed is a battery electrode having a high bulk density and a smooth surface with a small number of presses and a small press pressure. The present invention is not limited to these devices, and the smaller the temperature drop from the preheating portion to the heated press roll, the better.

【0014】[0014]

【実施例1】カーボン負極活物質をポリフッ化ビニリデ
ンが活物質に対し10重量部になるようにN−メチル−
2−ピロリドンに溶解した溶液に添加しスラリ−を得
た。このスラリ−を15μmの銅箔上の片面に塗布し乾
燥固化して130μmの塗膜を得た。
Example 1 A carbon negative electrode active material was prepared so that polyvinylidene fluoride was 10 parts by weight with respect to the active material.
It was added to a solution dissolved in 2-pyrrolidone to obtain a slurry. This slurry was applied to one surface of a 15 μm copper foil and dried and solidified to obtain a 130 μm coating film.

【0015】この塗膜を図1に示した加圧プレス機で予
備加熱、加熱プレスロールの温度を120℃に設定して
計7回プレスを行った。各プレス毎の活物質嵩密度の変
化を図3に示す。
The coating film was preheated by a press machine shown in FIG. 1 and pressed a total of seven times with the temperature of a heated press roll set at 120 ° C. FIG. 3 shows changes in the bulk density of the active material for each press.

【0016】[0016]

【実施例2】実施例1において図1に示す加圧プレス機
の加熱プレスロールを室温で使用した以外は同じ方法で
プレスした結果の活物質嵩密度の変化を図3に示す。
Example 2 FIG. 3 shows a change in the bulk density of the active material as a result of pressing in the same manner as in Example 1 except that the heated press roll of the press machine shown in FIG. 1 was used at room temperature.

【0017】[0017]

【実施例3】正極活物質としてのリチウムのコバルト酸
複合酸化物に導電剤として鱗片状グラファイトとアセチ
レンブラックを2.5重量部ずつ添加してコンパウンド
とした。次にこのコンパウンドに対し3重量部となるよ
うにフッ化ビニリデンのN−メチル−2−ピロリドン溶
液を添加してスラリーを得た。このスラリ−を15μm
のアルミ箔上の両面に塗布し乾燥固化して240μmの
塗膜を得た。得られた塗膜を図1に示した加圧プレス機
で予備加熱、加熱プレスロールの温度を120℃に設定
して線圧100kg/cm、200kg/cm、300
kg/cm、400kg/cmの4水準のプレス圧力条
件でそれぞれ3回プレスした。その時の正極活物質嵩密
度の変化を図4に示す。
Example 3 A compound was prepared by adding 2.5 parts by weight of flaky graphite and acetylene black as conductive agents to a cobalt oxide composite oxide of lithium as a positive electrode active material. Next, a solution of vinylidene fluoride in N-methyl-2-pyrrolidone was added so as to be 3 parts by weight with respect to this compound to obtain a slurry. This slurry is 15 μm
And coated and dried and solidified to obtain a coating film of 240 μm. The obtained coating film was pre-heated by the press shown in FIG. 1 and the temperature of the heated press roll was set to 120 ° C., and the linear pressure was set to 100 kg / cm, 200 kg / cm, and 300 kg / cm.
Pressing was performed three times under four levels of pressing pressure of kg / cm and 400 kg / cm. FIG. 4 shows the change in the bulk density of the positive electrode active material at that time.

【0018】[0018]

【実施例4】実施例3において図1に示す加圧プレス機
の加熱プレスロールを室温で使用した以外は同じ方法で
プレスした結果の正極活物質嵩密度の変化を図3に示
す。
EXAMPLE 4 FIG. 3 shows the change in the bulk density of the positive electrode active material as a result of pressing in the same manner as in Example 3 except that the heated press roll of the press shown in FIG. 1 was used at room temperature.

【0019】[0019]

【比較例1】実施例1において図1に示す加圧プレス機
の予備加熱部を使用しない以外は同じ方法でプレスした
結果の活物質嵩密度の変化を図3に示す。
Comparative Example 1 FIG. 3 shows the change in the bulk density of the active material as a result of pressing in the same manner as in Example 1 except that the preheating section of the press machine shown in FIG. 1 was not used.

【0020】[0020]

【比較例2】実施例1において図1に示す加圧プレス機
の予備加熱部を使用せず、しかもロールプレスを加熱し
ないで使用した以外は同じ方法でプレスした結果の活物
質嵩密度の変化を図3に示す。
Comparative Example 2 Changes in the bulk density of the active material as a result of pressing in the same manner as in Example 1 except that the preheating section of the press machine shown in FIG. 1 was not used and the roll press was used without heating. Is shown in FIG.

【0021】[0021]

【比較例3】実施例3において図1に示す加圧プレス機
の予備加熱部を使用せず、しかもロールプレスを加熱し
ないで使用した以外は同じ方法でプレスした結果の正極
活物質嵩密度の変化を図4に示す。
Comparative Example 3 The bulk density of the positive electrode active material as a result of pressing in the same manner as in Example 3 except that the preheating section of the press machine shown in FIG. 1 was not used and the roll press was used without heating was used. The changes are shown in FIG.

【0022】[0022]

【発明の効果】本発明によれば、少ないプレス回数、軽
いプレス圧で嵩密度が高く、平滑な表面を有する電池電
極が容易に得られる。
According to the present invention, a battery electrode having a high bulk density and a smooth surface can be easily obtained with a small number of presses and a small press pressure.

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

【図1】本発明の電池電極作成装置の概略断面図であ
る。
FIG. 1 is a schematic sectional view of a battery electrode forming apparatus of the present invention.

【図2】電池電極作成装置を構成する予備加熱部の概略
断面図である。
FIG. 2 is a schematic cross-sectional view of a preheating unit included in the battery electrode forming apparatus.

【図3】本発明の電池電極作成装置を用いた時の嵩密度
のプレス回数にともなう変化を示す図である。
FIG. 3 is a diagram showing a change in bulk density with the number of presses when using the battery electrode forming apparatus of the present invention.

【図4】本発明の電池電極作成装置を用いた時の嵩密度
のプレス条件に伴う変化を示す図である。
FIG. 4 is a diagram showing a change in bulk density with pressing conditions when using the battery electrode forming apparatus of the present invention.

【符号の説明】[Explanation of symbols]

1 巻だしロール 2 ガイド 3 予備加熱部 4 加熱プレスロール 5 巻取りロール 6 油圧シリンダー 7 積層体 8 加熱ドラム(小径) 9 加熱ドラム(大径) Reference Signs List 1 unwinding roll 2 guide 3 pre-heating unit 4 heating press roll 5 winding roll 6 hydraulic cylinder 7 laminated body 8 heating drum (small diameter) 9 heating drum (large diameter)

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 集電体上に活物質とバインダーを含む電
極合剤を形成してなる電池電極の製造方法において、前
記集電体上に電極合剤を塗布した積層体を予備加熱し、
次いで積層体を加圧プレスすることを特徴とする電池電
極の製造方法。
1. A method for manufacturing a battery electrode, comprising forming an electrode mixture containing an active material and a binder on a current collector, wherein a preliminarily heated laminate is prepared by applying the electrode mixture onto the current collector.
Next, a method for manufacturing a battery electrode, which comprises pressing the laminate under pressure.
【請求項2】 加圧プレスは加熱ロールプレスであるこ
とを特徴とする請求項1記載の電池電極の製造方法。
2. The method for manufacturing a battery electrode according to claim 1, wherein the pressure press is a heated roll press.
【請求項3】 集電体上に活物質、バインダを有する電
極合剤が形成された電池電極を製造する装置であって、
集電体上に電極合剤が塗布された積層体を送り出す巻出
し手段と、前記積層体を予備加熱する予備加熱手段と、
予備加熱された積層体を加熱、加圧する加熱加圧手段と
を備えたことを特徴とする電池電極の製造装置。
3. An apparatus for producing a battery electrode in which an electrode mixture having an active material and a binder is formed on a current collector,
Unwinding means for sending out the laminate coated with the electrode mixture on the current collector, and preheating means for preheating the laminate,
A device for manufacturing a battery electrode, comprising: a heating / pressurizing means for heating and pressurizing the preheated laminate.
JP9151097A 1997-06-09 1997-06-09 Manufacture of battery electrode and equipment thereof Withdrawn JPH113701A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9151097A JPH113701A (en) 1997-06-09 1997-06-09 Manufacture of battery electrode and equipment thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9151097A JPH113701A (en) 1997-06-09 1997-06-09 Manufacture of battery electrode and equipment thereof

Publications (1)

Publication Number Publication Date
JPH113701A true JPH113701A (en) 1999-01-06

Family

ID=15511280

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9151097A Withdrawn JPH113701A (en) 1997-06-09 1997-06-09 Manufacture of battery electrode and equipment thereof

Country Status (1)

Country Link
JP (1) JPH113701A (en)

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JP2002025535A (en) * 2000-07-07 2002-01-25 At Battery:Kk Battery
JP2002509341A (en) * 1997-12-12 2002-03-26 ミネソタ マイニング アンド マニュファクチャリング カンパニー Apparatus and method for treating cathode material provided on thin film substrate
JP2002324549A (en) * 2001-04-24 2002-11-08 Tdk Corp Manufacturing method for electrode for non-aqueous electrolyte battery and non-aqueous electrolyte secondary battery
US7510583B2 (en) 2004-04-21 2009-03-31 Ishikawajima-Harima Heavy Industries Co., Ltd. Cell electrode plate and process for producing the same
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WO2010106607A1 (en) * 2009-03-16 2010-09-23 パナソニック株式会社 Electrode plate for nonaqueous-electrolyte secondary battery, process for producing same, and nonaqueous-electrolyte secondary battery
US7967594B2 (en) 2005-01-25 2011-06-28 Ishikawajima-Harima Heavy Industries Co., Ltd. Facility for forming cell electrode plate
US8372538B2 (en) 2004-01-28 2013-02-12 Ishikawajima-Harima Heavy Industries Co., Ltd. Cell electrode plate and process for producing the same
WO2014164005A1 (en) * 2013-03-11 2014-10-09 Applied Materials, Inc. Electrode surface roughness control for spray coating process for lithium ion battery
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002509341A (en) * 1997-12-12 2002-03-26 ミネソタ マイニング アンド マニュファクチャリング カンパニー Apparatus and method for treating cathode material provided on thin film substrate
JP4959050B2 (en) * 1997-12-12 2012-06-20 スリーエム カンパニー Cathode material processing apparatus and method provided on thin film substrate
JP2002025535A (en) * 2000-07-07 2002-01-25 At Battery:Kk Battery
JP2002324549A (en) * 2001-04-24 2002-11-08 Tdk Corp Manufacturing method for electrode for non-aqueous electrolyte battery and non-aqueous electrolyte secondary battery
US8372538B2 (en) 2004-01-28 2013-02-12 Ishikawajima-Harima Heavy Industries Co., Ltd. Cell electrode plate and process for producing the same
US8377588B2 (en) 2004-01-28 2013-02-19 Ishikawajima-Harima Heavy Industries Co., Ltd. Cell electrode plate and process for producing the same
US7510583B2 (en) 2004-04-21 2009-03-31 Ishikawajima-Harima Heavy Industries Co., Ltd. Cell electrode plate and process for producing the same
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US7967594B2 (en) 2005-01-25 2011-06-28 Ishikawajima-Harima Heavy Industries Co., Ltd. Facility for forming cell electrode plate
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