JPS60167260A - Alkaline battery - Google Patents

Alkaline battery

Info

Publication number
JPS60167260A
JPS60167260A JP2373684A JP2373684A JPS60167260A JP S60167260 A JPS60167260 A JP S60167260A JP 2373684 A JP2373684 A JP 2373684A JP 2373684 A JP2373684 A JP 2373684A JP S60167260 A JPS60167260 A JP S60167260A
Authority
JP
Japan
Prior art keywords
battery
mixture
silver
thickness
apparent density
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
JP2373684A
Other languages
Japanese (ja)
Inventor
Tadao Takahashi
忠雄 高橋
Hiroyoshi Yoshihisa
吉久 洋悦
Takeisa Yokoyama
横山 武功
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.)
Yuasa Corp
Original Assignee
Yuasa Corp
Yuasa Battery Corp
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 Yuasa Corp, Yuasa Battery Corp filed Critical Yuasa Corp
Priority to JP2373684A priority Critical patent/JPS60167260A/en
Publication of JPS60167260A publication Critical patent/JPS60167260A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/06Electrodes for primary cells

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To increase the discharge capacity of an alkaline battery and enable it to be preserved for a longer period of time by pressing and fitting a mixture pellet composed of granulated silver peroxide and a silver peroxide powder into a positive case and forming a reduced layer having a restricted apparent density and thickness on the negative-electrode-side surface of the thus formed body. CONSTITUTION:A positive active material 2 consisting of a mixture of granulated silver peroxide (A) and a silver oxide powder (B) is compressed and molded into a given shape and the molded mixture is airtightly fitted into a positive case 1. Next, a reduced layer (C) with an apparent density of at least 5.5g/cm<2> and a thickness of at least 10mu is formed on the negative-electrode-4-side surface of the positive mixture. After that, the thus obtained body is installed facing a negative electrode 4 with a separator 3 impregnated with electrolyte interposed before sealing is performed using a gasket 6, thereby constituting an alkaline battery. As a result, due to the synergistic effect of the thickness and the apparent density of the reducing layer (C), the discharge capacity of the battery is increased and the battery can be preserved for a longer period of time.

Description

【発明の詳細な説明】 本発明は高性能なアルカリ電池に関するもので1その目
的は酸化銀の電位を有した放電容量が大きく、長期保存
性能のすぐれた電池を提供することにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a high-performance alkaline battery, and its object is to provide a battery having a silver oxide potential, a large discharge capacity, and excellent long-term storage performance.

近年小型携帯電子機器用電池として酸化銀電池が広く用
いられているが、最近では正極活物質として単位体積当
りの放電容量が酸化銀より大きい過酸化銀が単独で用い
られたり、過酸化銀を造粒し、酸化銀粉末と混合したも
のを用いることが検討されている。ところが過酸化銀を
正極活物質に用いた電池は、族1iti圧において過酸
化銀が酸化銀に還元される電圧1.8vと酸化銀が銀に
還元される電圧1.5vとの2段階となるために、酸化
銀電池との互換性に問題があった。酸化銀電池との互換
性を持たせるために、電池電圧を酸化銀→銀の1.5■
に制御させる必要があり1その方法として既に多くの提
案がなされている。原理的には正極活物質である過酸化
銀が正極端子を兼ねる正極容器と直接接触しないように
することで、例えば従来においては過酸化銀を主体とす
る正極活物質をペレット状に成形し、その全表面に還元
層を設けてペレットを被覆する方法や、過酸化銀造粒物
と酸化銀粉末との混合物を正極容器に充填し、その負極
対向面に還元剤を添加したta液により酸化銀と銀との
混合物から成る還元層を設け、電圧を制御する方法が広
く行なわれてきた。
In recent years, silver oxide batteries have been widely used as batteries for small portable electronic devices, but recently silver peroxide, which has a higher discharge capacity per unit volume than silver oxide, has been used alone as a positive electrode active material, or silver peroxide has been used alone as a positive electrode active material. The use of granulated silver oxide powder mixed with silver oxide powder is being considered. However, a battery using silver peroxide as the positive electrode active material has two stages: a voltage of 1.8 V at which silver peroxide is reduced to silver oxide, and a voltage of 1.5 V at which silver oxide is reduced to silver. Therefore, there was a problem with compatibility with silver oxide batteries. In order to have compatibility with silver oxide batteries, the battery voltage was changed from silver oxide to silver by 1.5■
There is a need to control the temperature of the air, and many proposals have already been made for this purpose. In principle, silver peroxide, which is the positive electrode active material, is prevented from coming into direct contact with the positive electrode container, which also serves as the positive electrode terminal. There is a method of coating the pellet by providing a reducing layer on its entire surface, or filling a positive electrode container with a mixture of silver peroxide granules and silver oxide powder, and oxidizing the surface facing the negative electrode with a TA solution containing a reducing agent. A method of controlling voltage by providing a reduction layer made of a mixture of silver and silver has been widely used.

しかしながら上記従来方法では還元層にムラが生じ、製
造直後には電圧制御ができていても、長期保存後に過酸
化銀→酸化銀の1.8vが出ることがあり、it電池量
を犠牲にして還元層の厚みを正極容量の数十パーセント
にまで厚くしこれを防止していた。
However, with the above conventional method, unevenness occurs in the reduction layer, and even if voltage control is possible immediately after manufacture, 1.8V of silver peroxide → silver oxide may be generated after long-term storage, resulting in sacrificing IT battery capacity. This was prevented by increasing the thickness of the reduced layer to several tens of percent of the positive electrode capacity.

本発明は上記欠点を解消するため、長期保存後に過酸化
銀→酸化銀の1.8vが出るのは、正極活物質が過酸化
銀造粒物と酸化銀粉末との混合物から成り、その負極対
向面のみに還元層を形成させたアルカリ電池の場合、そ
の厚みと見かけ密度が相互に影響しあうことに着目して
なされたもので、以下実施例により詳細に説明する0 第1図は本発明によるアルカリ電池の断面図で11は正
極端子を兼ねる正極容器、2は正極活物質、3は七パレ
ータ、4は負極活物質、5は負極端子を兼ねる負極容器
、6は封口剤ガスケットである。過酸化銀造粒物Aと酸
化銀粉末Bとの混合物から成る正極活物質2は、所定の
形に加圧成形され、正極容器1内に圧入、密着される。
In order to solve the above-mentioned drawbacks, the present invention aims to solve the problem that the positive electrode active material is made of a mixture of silver peroxide granules and silver oxide powder, and the negative electrode is made of a mixture of silver peroxide granules and silver oxide powder. In the case of an alkaline battery in which a reduced layer is formed only on the facing surface, this was done by focusing on the fact that the thickness and apparent density mutually influence each other. In the cross-sectional view of the alkaline battery according to the invention, 11 is a positive electrode container that also serves as a positive electrode terminal, 2 is a positive electrode active material, 3 is a seventh pallet, 4 is a negative electrode active material, 5 is a negative electrode container that also serves as a negative electrode terminal, and 6 is a sealant gasket. . A positive electrode active material 2 made of a mixture of silver peroxide granules A and silver oxide powder B is pressure-molded into a predetermined shape, and is press-fitted into the positive electrode container 1 and tightly attached thereto.

さらにその負極対向面には還元層Cを厚みhと見かけ密
度dを規制して形成させ、セパレータ3を載置し、負極
活物質4を充填した負極容器5を封口剤ガスチット6と
ともに正極容器1に圧着させている。
Furthermore, a reduction layer C is formed on the surface facing the negative electrode by regulating the thickness h and apparent density d, a separator 3 is placed thereon, and a negative electrode container 5 filled with a negative electrode active material 4 is placed on the positive electrode container 1 along with a gas sealant 6 as a sealant. It is crimped.

上記の如く還元層0の厚みhと見かけ密度dを規制して
製作した直径が7.Bztr、高さが1.6鯖の外形寸
法を有するアルカリ電池の長期保存性能を調査した結果
を表−1に示す0 表−1から還元層の厚みが同じであっても、見かけ密度
を大きくすると、長期保存性能は改善されることがわか
る。表−1の結果をさらに詳細に説明すれば、A3 、
A4の如く還元層の見かけ密度が4.5974では、そ
の後の加圧工程により還元層にヒビ割れを生じ3〜6ケ
月以上の長期保存後、電池電圧の制御ができなくなる。
The diameter produced by controlling the thickness h and apparent density d of the reduced layer 0 as described above is 7. Table 1 shows the results of investigating the long-term storage performance of alkaline batteries with external dimensions of 1.6 mm in height.0 From Table 1, even if the thickness of the reduced layer is the same, the apparent density can be increased. As a result, it can be seen that long-term storage performance is improved. To explain the results in Table 1 in more detail, A3,
If the apparent density of the reduced layer is 4.5974, such as in A4, the reduced layer will crack during the subsequent pressurization process, making it impossible to control the battery voltage after long-term storage of 3 to 6 months or more.

またA5.A9の如く還元層の見かけ密度が各々s、s
 9/d 、 6.59/cdであっても還元層の厚み
が小さすぎても同様である。以上のことから正極活物質
に過酸化銀造粒物と酸化銀粉末との混合物を用いたアル
カIJ を池では還元層の見かけ密度は5.59/d以
上で厚みは10μ以上であることが必要となる。
Also A5. As in A9, the apparent density of the reduced layer is s and s, respectively.
The same thing applies even if the thickness of the reduced layer is too small even if it is 9/d or 6.59/cd. From the above, it is found that in Alka IJ using a mixture of silver peroxide granules and silver oxide powder as the positive electrode active material, the apparent density of the reduced layer is 5.59/d or more and the thickness is 10 μ or more. It becomes necessary.

次に放電特性の比較を行ない、その結果を第2図に示す
。第2図においてビ)は表−1中A6の本発明電池、(
ロ)は本発明電池と同じ正極活物質を有し還元量を5.
s mムH/c−とした場合の電池、(ハ)は酸化銀の
みを正極活物質とした場合の電池それぞれ5ooooΩ
の負荷抵抗で放電を行なったものである。第2図から放
電持続時間は電池ピ)が860時間、電池(ロ)が82
0時間、電池(ハ)が620時間で、本発明電池の如く
負極対向面に還元層を形成させる場合、還元層の見かけ
密度と厚みの両方を規制した方が還元量を規制するより
放電容量が大きく長期保存性能がすぐれたものになるこ
とがわかる。
Next, the discharge characteristics were compared, and the results are shown in FIG. In Figure 2, B) is the A6 battery of the present invention in Table 1, (
B) has the same positive electrode active material as the battery of the present invention and has a reduction amount of 5.
s mm H/c-, (C) is a battery when only silver oxide is used as the positive electrode active material, each 5ooooΩ.
Discharge was performed with a load resistance of . From Figure 2, the discharge duration is 860 hours for battery P) and 82 hours for battery (B).
0 hour, and battery (C) for 620 hours, when a reduced layer is formed on the surface facing the negative electrode as in the battery of the present invention, it is better to control both the apparent density and thickness of the reduced layer than to control the amount of reduction. It can be seen that it has a large value and has excellent long-term storage performance.

以上述べた如く、本発明のアルカリ電池は従来電池に比
較して放電容量が大きく長期保存性能がすぐれていて、
近年の小IJJl携帯電子機儲用寛池として最適であり
、その工業的価値は大なるものである。
As described above, the alkaline battery of the present invention has a large discharge capacity and excellent long-term storage performance compared to conventional batteries.
It is most suitable for use in small IJJl portable electronic devices in recent years, and its industrial value is great.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明のアルカリ電池の断面図、第2図は放電
特性図である。 1・・・正&A容器 2・・・正極活物質3・・・七パ
レータ 4・・・負極活物質5・・・負極容器 6・・
・封口剤ガスケツトム・・・過酸化m造粒物 B・・・酸化銀粉末 O・・・還元層 出願人 湯浅電池株式会社 放 電 々 圧 CV) 200 400 600 800 1.000放電時間
(時間)
FIG. 1 is a sectional view of the alkaline battery of the present invention, and FIG. 2 is a discharge characteristic diagram. 1...Positive & A container 2...Positive electrode active material 3...7 palate 4...Negative electrode active material 5...Negative electrode container 6...
・Sealing agent gasket Tom...Peroxide m granules B...Silver oxide powder O...Reduction layer Applicant Yuasa Battery Co., Ltd. Discharge voltage CV) 200 400 600 800 1.000 Discharge time (hours)

Claims (1)

【特許請求の範囲】[Claims] 加圧成形してなる過酸化銀造粒物と酸化銀粉末との混合
物ペレットを正極答器内に圧入し、その負極対向面に見
かけ密度が5,597c++fで、厚みが10μ以上の
還元層を形成させ、電解液を浸潤させた七パレータを介
在させて、負極活物質を充填させた負極容器を対日用ガ
スケットとともに正極容器に圧着してなることを特徴と
するアルカリ電池。
A pellet of a mixture of pressure-molded silver peroxide granules and silver oxide powder is press-fitted into a positive electrode reactor, and a reduction layer with an apparent density of 5,597 c++f and a thickness of 10 μ or more is formed on the surface facing the negative electrode. 1. An alkaline battery characterized in that a negative electrode container filled with a negative electrode active material is press-bonded to a positive electrode container together with a sun-resistant gasket, with a seven-part plate formed and infiltrated with an electrolytic solution interposed therebetween.
JP2373684A 1984-02-09 1984-02-09 Alkaline battery Pending JPS60167260A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2373684A JPS60167260A (en) 1984-02-09 1984-02-09 Alkaline battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2373684A JPS60167260A (en) 1984-02-09 1984-02-09 Alkaline battery

Publications (1)

Publication Number Publication Date
JPS60167260A true JPS60167260A (en) 1985-08-30

Family

ID=12118590

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2373684A Pending JPS60167260A (en) 1984-02-09 1984-02-09 Alkaline battery

Country Status (1)

Country Link
JP (1) JPS60167260A (en)

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