JPH10154509A - Silver oxide battery - Google Patents

Silver oxide battery

Info

Publication number
JPH10154509A
JPH10154509A JP8313816A JP31381696A JPH10154509A JP H10154509 A JPH10154509 A JP H10154509A JP 8313816 A JP8313816 A JP 8313816A JP 31381696 A JP31381696 A JP 31381696A JP H10154509 A JPH10154509 A JP H10154509A
Authority
JP
Japan
Prior art keywords
positive electrode
silver oxide
active material
battery
electrode mixture
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
Application number
JP8313816A
Other languages
Japanese (ja)
Inventor
Mutsuo Nozawa
睦雄 野沢
Masashi Yamada
雅志 山田
Masahiro Ito
雅弘 伊藤
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.)
S I I MICRO PARTS KK
Original Assignee
S I I MICRO PARTS KK
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 S I I MICRO PARTS KK filed Critical S I I MICRO PARTS KK
Priority to JP8313816A priority Critical patent/JPH10154509A/en
Publication of JPH10154509A publication Critical patent/JPH10154509A/en
Pending 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 reduce an adding quantity of conductive auxiliaries, enhance density of a positive electrode mix and the ratio of an active material, realize large capacity of a battery, and improve a self-discharge characteristic by using flake-shaped graphite having a very wide plane as the conductive auxiliaries to a positive electrode active material. SOLUTION: Fig. is a cross-sectional drawing of a silver oxide battery. A positive electrode mixture 2 on which an adding quantity of graphite is set to 2%, a negative electrode mixture 4, electrolyte and a separator 3, are filled in a prescribed procedure in a positive electrode can 1, a negative electrode can 5 and a gasket 6 which become a vessel. The edge of the positive electrode can 1 is calked, and a battery is constituted. At this point, flake-shaped graphite on which a thickness is 0.5 to 9μm and an average diameter of a plane is 50t o 150μm, is used as the conductive auxiliaries of the positive electrode mix 2. A silver oxide on which an average particle diameter is 0.1 to 5μm may be used as a main positive electrode active material. Since density of the positive electrode mixture and the ratio of an active material are high, large electric capacity can be provided.

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、酸化銀電池の容量
ならびに自己放電特性の改善に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an improvement in the capacity and self-discharge characteristics of a silver oxide battery.

【0002】[0002]

【従来の技術】酸化銀電池の主たる活物質である酸化銀
は、電気伝導性が悪いため、導電助剤を必要とする。従
来、前述の導電助剤として、平均粒径、5μm程度の鱗
状黒鉛が使われており、中には、もう少し粒径の大き
い、10〜50μmの黒鉛を使用するものもあった。
(例えば、特公昭61−22422号公報参照) 従来、導電助剤の添加量は、活物質に対する重量比率
で、4〜10%程度が必要であった。この導電助剤の添
加量は、正極合剤の重量当たりの有効成分量および成形
密度に大きく影響を及ぼし、その量が少ないほど、正極
合剤の成形密度が高くかつ有効成分量の比率が大きい。
すなわち導電助剤が少ないほど、同一容積の缶の中によ
り多量の活物質を充填することができる。その量を減少
せしめる手段として、酸化銀の粒径を大きくする等の方
法が取られてきた(例えば、特公昭57−5342号広
報参照)。
2. Description of the Related Art Silver oxide, which is a main active material of a silver oxide battery, has poor electric conductivity and thus requires a conductive auxiliary. Conventionally, scale-like graphite having an average particle size of about 5 μm has been used as the above-mentioned conductive auxiliary agent, and some of them use graphite having a slightly larger particle diameter of 10 to 50 μm.
(See, for example, Japanese Patent Publication No. Sho 61-22422) Conventionally, the amount of the conductive additive to be added was about 4 to 10% by weight based on the active material. The addition amount of the conductive additive greatly affects the amount of the active ingredient per weight of the positive electrode mixture and the molding density, and the smaller the amount, the higher the molding density of the positive electrode mixture and the ratio of the amount of the active ingredient are large. .
That is, the smaller the amount of the conductive auxiliary agent, the more the active material can be filled in the same volume can. As a means for reducing the amount, methods such as enlarging the particle size of silver oxide have been adopted (for example, see JP-B-57-5342).

【0003】[0003]

【発明が解決しようとする課題】前述のように、従来の
技術では、まだ十分に導電助剤の量を減少せしめること
ができず、特に、酸化銀が通常の方法で製造された粒径
である、0.1〜5μmの範囲では特に多量に導電助剤
を添加する必要があるという問題点があった。また、酸
化銀の粒径を大きくすることは、コスト高になる欠点が
あった。
As described above, in the prior art, the amount of the conductive additive cannot be sufficiently reduced, and particularly, the silver oxide has a particle size produced by a conventional method. In a certain range of 0.1 to 5 μm, there is a problem that it is necessary to add a particularly large amount of the conductive assistant. Increasing the particle size of silver oxide has the disadvantage of increasing costs.

【0004】[0004]

【課題を解決するための手段】上記問題点を解決するた
めに、本発明は、非常に広い平面を有する薄片状の黒鉛
を正極活物質に対する導電助剤として用いた。その添加
量は、正極活物質に対する重量比率で、0.5〜3%
と、従来に比べ、大幅に低減した。本発明では、通常の
方法で製造した、0.1〜5μmの平均粒径を有する酸
化銀に対しても、前述の添加量で必要な機能を付与せし
めることができる。
In order to solve the above problems, the present invention uses flaky graphite having a very wide flat surface as a conductive additive for a positive electrode active material. The addition amount is 0.5 to 3% by weight based on the positive electrode active material.
, Significantly reduced compared to the past. In the present invention, the required functions can be imparted to the silver oxide having an average particle size of 0.1 to 5 μm, which is produced by a usual method, by the above-mentioned addition amount.

【0005】[0005]

【発明の実施の形態】本発明は、正極活物質に対する導
電助剤として、厚さ0.5〜9μm、平面の平均直径が
50〜150μmの薄片状の黒鉛を、酸化銀を主たる活
物質とする正極活物質に十分均一となるまで混合し、ペ
レット化して正極合剤として用いるものである。
BEST MODE FOR CARRYING OUT THE INVENTION According to the present invention, flaky graphite having a thickness of 0.5 to 9 μm and a plane average diameter of 50 to 150 μm is used as a conductive auxiliary for a positive electrode active material. The mixture is mixed until it is sufficiently uniform with the positive electrode active material to be formed, pelletized, and used as a positive electrode mixture.

【0006】正極の補助的な活物質として、二酸化マン
ガンが加えられても、同一の有効性を示す。前術の正極
合剤ペレットを、粒状のZnを主たる活物質とする負極
合剤、電解液、セパレータと共に、正極缶、ガスケット
と負極缶の中に充填し正極缶の口部をかしめて封止し、
電池として完成する。
[0006] Even if manganese dioxide is added as an auxiliary active material of the positive electrode, the same effectiveness is exhibited. Fill the positive electrode mixture pellets of the previous operation together with the negative electrode mixture containing granular Zn as the main active material, electrolyte solution, and separator into the positive electrode can, gasket and negative electrode can, and seal the mouth of the positive electrode can by caulking And
Completed as a battery.

【0007】本発明の黒鉛の寸法形状の規制範囲は、黒
鉛自体の製造能力によるものであって、この範囲を越え
たものは、その製造が困難となり、現時点では、実質的
な有効性を有しない。厚さの点では、9μmよりも厚い
ものを製造することは可能であるが、厚さが厚くなるに
つれて黒鉛の添加量を増やさなければならず、本発明の
添加重量比の範囲を保つためには、厚さ5μ以下が好ま
しい。
The restricted range of the size and shape of the graphite of the present invention depends on the production capacity of the graphite itself. If the range exceeds this range, it becomes difficult to produce the graphite. At present, the graphite has substantial effectiveness. do not do. In terms of thickness, it is possible to produce a material having a thickness of more than 9 μm, but as the thickness increases, the amount of graphite must be increased, and in order to maintain the range of the weight ratio of the present invention. Is preferably 5 μm or less in thickness.

【0008】黒鉛が正極合剤中に占める割合が、0.5
%を下回ると、ペレットに成形する際に金型に加工粉が
付着して、通常金型のかじりと呼ばれる現象をおこし成
形し難い。黒鉛が、正極合剤中に占める比率が3%を越
えると、従来技術によるものとの差が小さくなり本発明
の優位性が薄れる。従って、本発明、正極合剤中に占め
る黒鉛の比率を、0.5〜3%とすることが適切であ
る。
[0008] The proportion of graphite in the positive electrode mixture is 0.5%.
%, The processing powder adheres to the mold at the time of molding into pellets, and usually causes a phenomenon called galling of the mold, making molding difficult. When the ratio of graphite in the positive electrode mixture exceeds 3%, the difference from the prior art is reduced and the advantage of the present invention is reduced. Therefore, in the present invention, it is appropriate that the ratio of graphite in the positive electrode mixture is 0.5 to 3%.

【0009】[0009]

【実施例】【Example】

(実施例1)微粉酸化銀と呼ばれている、通常の方法で
製造した平均粒径0.1〜5μmの酸化銀の粉末と補助
的な活物質である二酸化マンガンと前述の厚さ0.5〜
9μm、平面の平均直径が50〜150μmの黒鉛を混
合機を用いて混合した。黒鉛の全合剤重量に占める重量
比率は、0.5、1、2、3、5の5水準である。この
混合粉末を、成形機により、約5.5t/cm2の成形
圧力で成形し、外径6.4mm、厚さ0.8mmのペレ
ットとした。
(Example 1) Powder of silver oxide having a mean particle size of 0.1 to 5 µm, which is referred to as finely divided silver oxide, and having an average particle diameter of 0.1 to 5 µm, manganese dioxide as an auxiliary active material, and the above-mentioned thickness of 0.1 µm. 5-
9 μm, graphite having a plane average diameter of 50 to 150 μm was mixed using a mixer. The weight ratio of graphite to the total weight of the mixture is five levels of 0.5, 1, 2, 3, and 5. This mixed powder was molded by a molding machine at a molding pressure of about 5.5 t / cm 2 to obtain pellets having an outer diameter of 6.4 mm and a thickness of 0.8 mm.

【0010】前述のペレットと、従来より使用されてい
る黒鉛を使用したペレットとを、平板の表面をAuめっ
きした端子間に挟み、接触荷重50gで端子間の抵抗値
を測定した。その測定結果を表1に示す。
[0010] The above-mentioned pellet and a pellet using graphite conventionally used were sandwiched between Au-plated terminals on the surface of a flat plate, and the resistance value between the terminals was measured with a contact load of 50 g. Table 1 shows the measurement results.

【0011】[0011]

【表1】 [Table 1]

【0012】この結果、測定不能のペレットは、製造直
後の電池の電流電圧特性が悪く、使用に耐えない。ペレ
ットの抵抗が、数kΩの段階から、電池の初期的な電気
特性は若干低いが、放電の進行とともに、導電性の良好
な銀が生成されて、リードがとれやすくなるため、使用
可能の範囲に含まれる。本発明のペレットは、いずれも
使用可能の範囲に含まれていることが分かる。
As a result, the unmeasurable pellets have poor current-voltage characteristics of the battery immediately after production and cannot be used. From the stage where the resistance of the pellet is several kilohms, the initial electrical characteristics of the battery are slightly low, but with the progress of discharge, silver with good conductivity is generated and the lead is easily removed, so the usable range is include. It can be seen that the pellets of the present invention are all included in the usable range.

【0013】(実施例2)以下の手順で、本発明の酸化
銀電池SR626SWを製造した。図1はその概要を示
す断面図である。前述の実施例1のペレットの内、黒鉛
の添加量が2%のものを正極合剤2とし、負極合剤4、
電解液、セパレータ3を容器である正極缶1、負極缶
5、ガスケット6に所定の手順で充填し、正極缶の縁を
かしめて電池とした。図中、電解液は指示されていない
が、内部全体に拡散している。
Example 2 A silver oxide battery SR626SW of the present invention was manufactured by the following procedure. FIG. 1 is a sectional view showing the outline. Among the pellets of Example 1 described above, those having a graphite addition amount of 2% were used as the positive electrode mixture 2, and the negative electrode mixture 4,
The electrolytic solution and the separator 3 were filled in the container, the positive electrode can 1, the negative electrode can 5, and the gasket 6 according to a predetermined procedure, and the edge of the positive electrode can was caulked to obtain a battery. In the figure, the electrolyte is not indicated, but is diffused throughout the inside.

【0014】この本発明の電池と従来の電池の容量なら
びに、60℃の環境に20日間保存した後の容量を比較
した。表2にその結果を示す。試験数は各6個で、表の
数値はその平均値である。
The capacity of the battery of the present invention and the capacity of a conventional battery and the capacity after storage in an environment of 60 ° C. for 20 days were compared. Table 2 shows the results. The number of tests is six each, and the values in the table are the average values.

【0015】[0015]

【表2】 [Table 2]

【0016】[0016]

【発明の効果】上記のように構成された酸化銀電池は、
正極合剤の密度並びに活物質の比率が高いため、同一の
内容積の従来のものに比べ、大きい電気容量を持たせる
ことができる。かつ、導電助剤である炭素の量は、例え
ば、特公昭61−22422号広報にも示されているよ
うに、自己放電と関係し、その量が少ないほど保存率が
よい。本発明は、従来よりも容量、並びに自己放電特性
に優れていることは、実施例により明らかである。
The silver oxide battery constructed as described above has the following features.
Since the density of the positive electrode mixture and the ratio of the active material are high, a larger electric capacity can be provided as compared with a conventional one having the same internal volume. The amount of carbon, which is a conductive additive, is related to self-discharge as shown in, for example, Japanese Patent Publication No. 61-22422, and the smaller the amount, the better the storage rate. It is clear from the examples that the present invention is more excellent in the capacity and the self-discharge characteristic than the conventional one.

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

【図1】本発明の実施例の酸化銀電池の概要を示す断面
図である。
FIG. 1 is a sectional view showing an outline of a silver oxide battery according to an embodiment of the present invention.

【符号の説明】[Explanation of symbols]

1 正極缶 2 正極合剤 3 セパレター 4 負極合剤 5 負極缶 6 ガスケット 1 Positive electrode can 2 Positive electrode mixture 3 Separator 4 Negative electrode mixture 5 Negative electrode can 6 Gasket

フロントページの続き (72)発明者 伊藤 雅弘 宮城県仙台市太白区西多賀5丁目30番1号 株式会社エスアイアイ・マイクロパーツ 内Continuation of the front page (72) Inventor Masahiro Ito 5-30-1, Nishitaga, Taihaku-ku, Sendai-shi, Miyagi SII Micro Parts Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 正極合剤、負極合剤、アルカリ電解液、
セパレータ、正極缶、負極缶、ガスケットを主たる構成
要素とし、該正極合剤が、平均厚さ0.5〜9μm、広
い面側の平均直径が50〜150μmである薄片状の黒
鉛を、活物質に対する重量比率で0.5〜3%添加混合
したものであることを特徴とする酸化銀電池。
1. A positive electrode mixture, a negative electrode mixture, an alkaline electrolyte,
A separator, a positive electrode can, a negative electrode can, and a gasket are main components, and the positive electrode mixture is flaky graphite having an average thickness of 0.5 to 9 μm and an average diameter on a wide surface side of 50 to 150 μm. A silver oxide battery characterized by being added and mixed in a weight ratio of 0.5 to 3% based on the weight of the silver oxide battery.
【請求項2】 平均粒径が0.1〜5μmの酸化銀を主
たる正極活物質とする請求項1記載の酸化銀電池。
2. The silver oxide battery according to claim 1, wherein silver oxide having an average particle size of 0.1 to 5 μm is mainly used as a positive electrode active material.
JP8313816A 1996-11-25 1996-11-25 Silver oxide battery Pending JPH10154509A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8313816A JPH10154509A (en) 1996-11-25 1996-11-25 Silver oxide battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8313816A JPH10154509A (en) 1996-11-25 1996-11-25 Silver oxide battery

Publications (1)

Publication Number Publication Date
JPH10154509A true JPH10154509A (en) 1998-06-09

Family

ID=18045864

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8313816A Pending JPH10154509A (en) 1996-11-25 1996-11-25 Silver oxide battery

Country Status (1)

Country Link
JP (1) JPH10154509A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009224077A (en) * 2008-03-13 2009-10-01 Fdk Energy Co Ltd Cathode mixture for alkaline battery and alkaline battery

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009224077A (en) * 2008-03-13 2009-10-01 Fdk Energy Co Ltd Cathode mixture for alkaline battery and alkaline battery

Similar Documents

Publication Publication Date Title
JP5453243B2 (en) Alkaline chemical battery
US7524582B2 (en) Zinc powder or zinc alloy powder for alkaline batteries
JPH07272715A (en) Alkaline manganese battery
US4427751A (en) Alkaline battery
SK47697A3 (en) Alkaline galvanic cell and manufacturing process thereof
EP0503287A1 (en) Zinc alkaline cells
EP0503288A1 (en) Zinc alkaline cells comprising non amalgamated zinc alloy powder as anodic material
JP3215447B2 (en) Zinc alkaline battery
JPH10154509A (en) Silver oxide battery
JP2000164220A (en) Electrode material for silver oxide battery
JP3505823B2 (en) Flat alkaline battery
JPH0212762A (en) Silver oxide battery
JP3505824B2 (en) Flat alkaline battery
WO2024105934A1 (en) Alkaline battery and method for manufacturing alkaline battery
JPS58178959A (en) Method of producing compression cathode for chemical battery
JPS62226563A (en) Nonaqueous electrolyte secondary battery
JP2001068170A (en) Zinc air battery
JPS6091562A (en) Cylindrical alkali battery
JPS60240056A (en) Alkaline-manganese cell
JPH07272714A (en) Nonaqueous electrolyte battery
JPS59139556A (en) Manufacturing method of positive electrode black mix for solid electrolyte battery
JPH07130364A (en) Nickel electrode for alkaline storage battery and alkaline storage battery using the electrode
JPH08241708A (en) Manufacture of positive electrode mixture for alkaline-manganese battery
JPH09320589A (en) Silver oxide battery
JPS6369145A (en) Silver oxide battery