JPS6023967A - Plate battery - Google Patents
Plate batteryInfo
- Publication number
- JPS6023967A JPS6023967A JP13216583A JP13216583A JPS6023967A JP S6023967 A JPS6023967 A JP S6023967A JP 13216583 A JP13216583 A JP 13216583A JP 13216583 A JP13216583 A JP 13216583A JP S6023967 A JPS6023967 A JP S6023967A
- Authority
- JP
- Japan
- Prior art keywords
- positive
- negative
- battery
- conductive plastic
- active materials
- 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.)
- Pending
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
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
-
- 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
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/668—Composites of electroconductive material and synthetic resins
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/04—Cells with aqueous electrolyte
- H01M6/06—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid
- H01M6/12—Dry cells, i.e. cells wherein the electrolyte is rendered non-fluid with flat electrodes
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Composite Materials (AREA)
- Cell Electrode Carriers And Collectors (AREA)
- Primary Cells (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、薄くかつフレキシブルなアルカリマンガン及
びルクランシエ系の平板型電池に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a thin and flexible alkaline manganese and Lecrancier type flat plate battery.
一般に平板現電池の構造は図−1に示すように、正、負
極集電体1,6としてS電性プラスチックフィルム(以
後導ブラと略す)にアルミニウム箔(At箔〕を接置さ
せたラミネートフィルムを用い、前記正極集電体lに二
酸化マンガンを主体とする正極活物質層2af塗眉させ
、その上にセパレータ3αを配置し、次に予め導プラ4
に亜鉛末層5cLと二酸化マンガン層2bf塗着させた
デュプレックス電極を配直し、その上にセパレータ3b
、次いで前記負極集電体6に予め亜鉛末層5bを塗着し
た乾燥バッチを配置していた。この電池は平板型である
ため電極面積が大きくかつ極間距離を小さくすることが
可能で、大電流を取シ出せることが特徴であった。そこ
で、カメラのフィルム送シ出し用の小型モータの駆動、
ストロボ。Generally, the structure of a flat plate current battery is as shown in Figure 1. The positive and negative electrode current collectors 1 and 6 are a laminate in which aluminum foil (At foil) is placed on an S conductive plastic film (hereinafter abbreviated as conductor). Using a film, the positive electrode active material layer 2af mainly composed of manganese dioxide is coated on the positive electrode current collector l, a separator 3α is placed on top of the positive electrode active material layer 2af, and then a conductive layer 4
The duplex electrode coated with 5cL of zinc dust layer and 2bf of manganese dioxide layer is rearranged, and a separator 3b is placed on top of it.
Next, a dry batch on which the zinc dust layer 5b was applied in advance was placed on the negative electrode current collector 6. Since this battery is of a flat plate type, the electrode area is large and the distance between the electrodes can be made small, making it possible to draw a large current. Therefore, we decided to drive a small motor for advancing the camera's film.
strobe.
フラッシュの瞬間充電用の電源等に使わnていた。こt
らは、いず扛も大電流消費型のハイパワーグレード電池
を要求する機器でろシ、他にミスカミソリ、小型強化ラ
イト、小型無線機等が必る。It was used as a power source for instant flash charging. This
These are all devices that require high-power grade batteries that consume large currents, as well as razors, small reinforced lights, and small radios.
近年、電池を内蔵するマイクロエレクトロニクス機器の
傾向は、軽薄短小化が促進さ7L、この動きに伴ない集
積回路技術が向上し低消費電力化が急速に進行している
。なかでも電子ウォッチ、電子ゲーム、ペソモジュール
等小型電子機器においては、消*電流が1〜2μ八程度
へ1で低下してきた。こうした背景の中で、電池にも小
型薄を化の要求が強く、ボタン型銀電池では1閣を割シ
O68調の厚さ1でに達している。そこで電池に対して
今後要求さ7しる内容は、小型電子機器をさらに小さく
薄くするために厚さを極限まで薄くすることと同時に、
小型電子様器のいくらかのデッドスペースを活用できる
ような変形自在のフレキシブル特性である。In recent years, the trend in microelectronic devices with built-in batteries has been toward smaller, lighter, thinner, and smaller devices.This trend has led to improvements in integrated circuit technology and rapid reductions in power consumption. In particular, in small electronic devices such as electronic watches, electronic games, and peso modules, the extinction current has decreased to about 1 to 2 μ8. Against this background, there is a strong demand for batteries to be smaller and thinner, and button-type silver batteries have reached a thickness of 1 inch, which is equivalent to O68. Therefore, what will be required of batteries in the future is to reduce the thickness to the absolute minimum in order to make small electronic devices even smaller and thinner.
It has a flexible characteristic that allows it to be deformed and makes use of some dead space in small electronic devices.
従来の平板現電池は、正、負極集電体として導ブラに5
0μ淋程度のAt箔をラミネートしているため、可撓性
が低く大きなフレキシブル特性をもたせることが困難で
あった。また、電池厚さも1〜2周までの追求であシ、
前記ボタン型銀電池にも及ばなかった。ボタン現電池の
場合は、外装ケースとして金属缶を使用しているため、
薄さには限界からシ、当然フレキシブル特性は有してい
ない。Conventional flat plate batteries have five conductors as positive and negative current collectors.
Since the At foil is laminated with a thickness of approximately 0 μm, flexibility is low and it is difficult to provide large flexibility characteristics. In addition, the battery thickness must be increased to 1 to 2 laps.
It was also not as good as the button-type silver battery. In the case of button current batteries, a metal can is used as the outer case, so
There is a limit to its thinness, and it naturally does not have flexible properties.
本発明は、以上のような欠点を除去し、極めて薄くかつ
フレキシブルな平板状電池を提供するものであり、以下
その実施例を第2図に沿って説明する。The present invention eliminates the above-mentioned drawbacks and provides an extremely thin and flexible flat battery.Examples thereof will be described below with reference to FIG. 2.
矢2図に示す平板型電池は第1図に示した平板型電池と
同じ電圧に!するVタイプの構造である。1及び6は厚
さ10μηLの導プラでそ7tぞれ正1負極の集電体で
るる。4も同じ導ブラを使用している。この導ブラはニ
トリルブタジェンゴムをペースとして酢酸ビニルと塩化
ビニルの共重合体をブレンドしさらに導電性を得るため
にカーボンプラック全15%添加したものである。当然
ながらこの導プラは集電体及び電極として導電性を眉し
かつ耐電解液性があるもので62Lば良い。たとえば、
ポリエチレンにカーボンブラックを添〃口しrv4ブラ
等がある。The flat battery shown in Figure 2 has the same voltage as the flat battery shown in Figure 1! It has a V-type structure. 1 and 6 are conductive plastics with a thickness of 10μηL, and 7t are current collectors for positive and negative electrodes, respectively. 4 also uses the same conductor. This conductor is made by blending a copolymer of vinyl acetate and vinyl chloride with nitrile butadiene rubber as a base, and further adding 15% carbon plaque in total to obtain conductivity. Naturally, this conductor plastic should be conductive as a current collector and an electrode, and should be resistant to electrolyte, and only needs to be 62L. for example,
There are RV4 bras made by adding carbon black to polyethylene.
こnらの導ブラは、集電性を高めるためカーボンブラッ
ク添刀n量?:調整した結果、体蹟抵抗率が5〜8X1
03Ω−m、表面抵抗率が3〜5x10Ωの導ブラが得
らnた。Are these conductors coated with carbon black to improve current collection? :As a result of adjustment, the body resistance is 5~8X1
A conductor with a surface resistivity of 3 to 5 x 10 Ω was obtained.
2α、2bは二酸化マンガンを主体とする正極活物質で
7厚さf 20 p mに規制し7ヒ。この正極活物質
2a、2bは専プラ1,4に予めスクリーン印刷、グラ
ビア印刷、スキージング、押し出し法等の一般の塗布方
法を用いて塗着さぜた。3a、3bは酸化銀電池等で使
わしている厚さ10μmのブドーセロハンを用いた。5
α、5bは亜鉛末ないし水化亜鉛を主体とする負極活物
質で、正極活質2α、2bと同様に前記一般の塗布方法
によ勺厚さ5μ常に規制した。電解液は9N水酸化カリ
ウム溶液及び塩化亜鉛35wt%、塩化アンモニウム3
wt飴の″rM、解液の酢液類について実施した。第1
表はこしらをまとめた組成表である。なお、電池周辺部
の封口は、導ブラとの密着性を強化するπめに、導ブラ
の一成分である酢酸ビニルと塩化ビニルの共重合体のエ
マルジョンをセパレーターに予め塗布しておき、組立時
に熱圧着によシシールした。2α and 2b are positive electrode active materials mainly composed of manganese dioxide, and the thickness is regulated to f 20 p m. The positive electrode active materials 2a and 2b were applied to the special plastics 1 and 4 in advance using a general coating method such as screen printing, gravure printing, squeegeeing, and extrusion. For 3a and 3b, 10 μm thick cellophane cellophane used in silver oxide batteries, etc. was used. 5
α and 5b are negative electrode active materials mainly composed of zinc powder or zinc hydrate, and the coating thickness was always regulated to 5 μm using the above-mentioned general coating method, similarly to the positive electrode active materials 2α and 2b. The electrolyte is 9N potassium hydroxide solution, 35wt% zinc chloride, 3% ammonium chloride.
The experiment was carried out on ``rM'' of wt candy and vinegar solution of dissolved solution.First
The table below is a composition table that summarizes the ingredients. To seal the area around the battery, in order to strengthen the adhesion with the conductor, apply an emulsion of a copolymer of vinyl acetate and vinyl chloride, which is one of the components of the conductor, to the separator in advance. At that time, it was sealed by heat compression bonding.
第 ・1 表
以上のように製造さnfc電池は、厚さがO01瓢と極
めて薄くかつ柔軟性に富み、電池中央部で90°に曲げ
た場合にも平板状と同一の特性を有することができた。Table 1 The NFC battery manufactured as shown above is extremely thin and flexible, with a thickness of O01, and even when bent at 90 degrees at the center of the battery, it has the same characteristics as a flat plate. did it.
第3図に、電池電極面と同一形状大きさの外部電極を接
続して測定した電流−電圧曲綜を示す。FIG. 3 shows a current-voltage curve measured by connecting an external electrode having the same shape and size as the battery electrode surface.
このように、小型電子機器の消費電流に必要な電流を十
分に取シ出せるばかシでなく、極めて薄くフレキシブル
な電池は、自由な形状の電池の製造をも可能にし、小型
電子機器の小型薄型化を実現しうる丸めに大きな貢献金
するものと期待できる。さらに、実施例では3■タイプ
の平板型電池を示したが、1゜5■タイプの場合は0゜
05mmまで薄くすることが確認さEている。In this way, an extremely thin and flexible battery that is not only able to draw enough current to meet the current consumption of small electronic devices will also make it possible to manufacture batteries of any shape, making it possible to produce small, thin, and small electronic devices. It is expected that this will make a significant contribution to the rounding process that will make it possible to achieve this goal. Further, in the example, a 3-inch type flat plate battery was shown, but it has been confirmed that the thickness can be reduced to 0.05 mm in the case of a 1° 5-inch type.
第1図は従来の平板型電池。第2図は本発明による平板
型電池。1゜。正極集電体、2゜。正極活物質、3゜、
セパ1/−タ、4゜。中間集電体、5゜。口極活物看、
6゜。9極集電体。第3図は、本発明の実施例によシ得
らnた電流−電圧曲線。IA、。アルカリタイプ、IB
、、アルカリタイプf:90°曲げた場合、2A、、ル
クランシエタイプ、2B。。ルクランシエタイプを90
°曲げた場合。 以上Figure 1 shows a conventional flat plate battery. FIG. 2 shows a flat plate battery according to the present invention. 1°. Positive electrode current collector, 2°. Positive electrode active material, 3°,
Separate 1/-ta, 4°. Intermediate current collector, 5°. Kuchiku live animal observation,
6°. 9-pole current collector. FIG. 3 is a current-voltage curve obtained according to an embodiment of the present invention. I.A. Alkaline type, IB
,,Alkali type f: 90° bending, 2A,,Lecrancier type, 2B. . Le Clancier type 90
°When bent. that's all
Claims (1)
セパレークに不織布、セロハンまた(はクラフトポリエ
チレン、電解液に水酸化カリウム溶液°または水酸化ナ
トリウム溶液あるいは塩化亜鉛および塩化アンモニウム
の混合液を用いる一次電池において、導電住プラスチッ
クフィルムを正、負極集電体力)つ正、負極端子とし1
とことを特徴とする平板型電池。Manganese dioxide for the positive electrode, zinc powder or frozen zinc for the negative electrode,
In primary batteries that use non-woven fabric, cellophane or (or kraft polyethylene) as the separator, and a potassium hydroxide solution or sodium hydroxide solution or a mixed solution of zinc chloride and ammonium chloride as the electrolyte, conductive plastic films are used as positive and negative electrode current collectors. ) positive and negative terminals and 1
A flat plate battery characterized by a.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13216583A JPS6023967A (en) | 1983-07-20 | 1983-07-20 | Plate battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13216583A JPS6023967A (en) | 1983-07-20 | 1983-07-20 | Plate battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6023967A true JPS6023967A (en) | 1985-02-06 |
Family
ID=15074881
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13216583A Pending JPS6023967A (en) | 1983-07-20 | 1983-07-20 | Plate battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6023967A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0275883A2 (en) * | 1987-01-15 | 1988-07-27 | Lonza Ag | Application for a dispersion for coatiing battery cathodes |
JPH0247768U (en) * | 1988-09-27 | 1990-04-03 | ||
KR100760748B1 (en) * | 1997-06-12 | 2007-09-21 | 파워 페이퍼 리미티드 | Flexible thin layer open electrochemical cell and applications of same |
-
1983
- 1983-07-20 JP JP13216583A patent/JPS6023967A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0275883A2 (en) * | 1987-01-15 | 1988-07-27 | Lonza Ag | Application for a dispersion for coatiing battery cathodes |
JPH0247768U (en) * | 1988-09-27 | 1990-04-03 | ||
KR100760748B1 (en) * | 1997-06-12 | 2007-09-21 | 파워 페이퍼 리미티드 | Flexible thin layer open electrochemical cell and applications of same |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5436091A (en) | Solid state electrochemical cell having microroughened current collector | |
GB2063553A (en) | Manufacture of laminates for use in cells | |
JP3198828B2 (en) | Manufacturing method of all solid lithium secondary battery | |
CN107565170B (en) | A kind of chemical synthesizing method of lithium ion battery | |
WO2000013252A1 (en) | Method for producing nonaqueous gel electrolyte cell | |
JPH10270013A (en) | Electrode for nonaqueous electrolyte secondary battery and its manufacture | |
JPH0222982B2 (en) | ||
JP3260310B2 (en) | Manufacturing method of sheet type electrode / electrolyte structure | |
JPS6023967A (en) | Plate battery | |
JPH0883596A (en) | Thin card battery | |
JP4283518B2 (en) | Electrochemical devices | |
JPH1167277A (en) | Lithium secondary battery | |
JPS63289768A (en) | Solid electrolyte battery | |
JP3240650B2 (en) | Manufacturing method of solid state secondary battery | |
JP3348236B2 (en) | Air electrode current collecting material for air battery using alkaline electrolyte and air battery using alkaline electrolyte provided with the same | |
JPH11144709A (en) | Electrode for electrochemical element and manufacture | |
JP2003297337A (en) | Electrode structure, its manufacturing method, and secondary battery | |
CN110752383A (en) | Flexible battery and preparation method thereof | |
CN220138351U (en) | Disposable lithium-manganese battery | |
JP2000348774A (en) | Manufacture of secondary battery | |
CN210628417U (en) | Flexible battery | |
JPH0576138B2 (en) | ||
JP3705694B2 (en) | Alkaline manganese battery | |
JP2001229975A (en) | Nonaqueous secondary battery and manufacturing method therefor | |
JPS5848364A (en) | Solid electrolyte battery |