JPS5851477A - Silver-oxide battery - Google Patents

Silver-oxide battery

Info

Publication number
JPS5851477A
JPS5851477A JP56148301A JP14830181A JPS5851477A JP S5851477 A JPS5851477 A JP S5851477A JP 56148301 A JP56148301 A JP 56148301A JP 14830181 A JP14830181 A JP 14830181A JP S5851477 A JPS5851477 A JP S5851477A
Authority
JP
Japan
Prior art keywords
active material
silver
battery
positive active
silver oxide
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
JP56148301A
Other languages
Japanese (ja)
Inventor
Hiroshi Ishiuchi
石内 博
Kimitaka Koseki
小関 公崇
Yasuharu Tominaga
富永 安治
Hachiro Azuma
東 八郎
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.)
Maxell Ltd
Original Assignee
Hitachi Maxell 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 Hitachi Maxell Ltd filed Critical Hitachi Maxell Ltd
Priority to JP56148301A priority Critical patent/JPS5851477A/en
Publication of JPS5851477A publication Critical patent/JPS5851477A/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
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/54Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of silver
    • 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

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

Abstract

PURPOSE:To enable a silver-oxide battery to be made thin by improving the weighing accuracy and the moldability of a positive active material by using as the positive active material, silver-oxide granules having specified grain diameters and a specified bulk density. CONSTITUTION:Silver-oxide powder is made into granules with diameters of 50-500mu and a bulk density of 1.5-3.5g/cm2, and the granules are used as a positive active material. By the means mentioned above, since the fluidity of the positive active material can be widely improved compared to a powdery active material, the weighing accuracy and the moldability are increased. As a result, the variation in the packed amount of the positive active material is reduced even in manufacturing a thin battery. In addition, the moldability during the press molding of the positive mixture is increased. Consequently, a silver-oxide battery with a reduced generation of formation deficiency can be obtained.

Description

【発明の詳細な説明】 本発明は酸化銀電池の改良に係り、酸化銀を顆粒化し、
秤量性、成形性を向上させ、薄形電池の提供を可能なら
し、めることを目的とするO従来、酸化**池の正極活
物質には粒径0.1〜10uswの酸化銀(Ag20ま
たはAge)粉末が使用されていたが、流動性が急く、
そのため秤量性、成形性が悪く、特に正極活物質の充填
量が少ない薄形電池では充填量のバラツキが大きくなり
、また加圧成形時の不良発生率が高くなるという問題が
あった。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improvement of silver oxide batteries, by granulating silver oxide,
The purpose is to improve weighability and moldability, and to make it possible to provide thin batteries. Conventionally, silver oxide (with a particle size of 0.1 to 10 usw) is used as a positive electrode active material in an oxidation pond. Ag20 or Age) powder was used, but the fluidity is fast,
Therefore, weighability and moldability are poor, and in particular, in thin batteries with a small amount of positive electrode active material filled, there are problems in that the filling amount varies widely and the failure rate during pressure molding increases.

そこで電子伝導性の付与を兼ねて正極活物質にシん状黒
鉛を添加することが行なわれているが、充分な活動性を
付与するには体積的にかなりのりん状黒鉛を僑加しなけ
ればならず、そのため放電容量が低下して高容量化がは
かれないという欠点がある。
Therefore, phosphorous graphite is added to the positive electrode active material to provide electron conductivity, but in order to provide sufficient activity, a considerable amount of phosphorous graphite must be added in terms of volume. However, this has the disadvantage that the discharge capacity decreases and it is not possible to increase the capacity.

本発明者らはそのような事情に鎌み植々研兇を重ねた結
果、酸化銀粉末を粒径50〜500μm1力サ密度1.
5〜!i、5 f/cm2に顆粒化し、核酸化銀顆粒を
正極活物質として用いるときは、粉末状のものを用いる
場合に比べて流動性が大中に改良され、抑振性ならびに
成形性が向上して、正極活物質の充填量が少ない薄形電
池の場合でも光横蓋のバラツキが少なく、かつ加圧成形
時の成形性が向上して成形不良の発生が少ない酸化銀電
池が得られることを見出し、本発明を完成するにいたっ
た。
The inventors of the present invention have repeatedly studied this situation and found that silver oxide powder has a particle size of 50 to 500 μm, a force density of 1.
5~! i, When granulated to 5 f/cm2 and used as a positive electrode active material, silver oxide granules have significantly improved fluidity and improved vibration suppression and moldability compared to when using powdered silver oxide granules. By doing so, it is possible to obtain a silver oxide battery with less variation in the optical side cover even in the case of a thin battery with a small filling amount of positive electrode active material, and with improved moldability during pressure molding and with less occurrence of molding defects. They discovered this and completed the present invention.

本発明において用いる前記のごとき酸化銀顆粒を得るに
は、たとえば通常の粒径0.1〜10μsgo#を化銀
粉末を水でスラリー状にし、造粒機で造粒し、好ましく
は球形整粒機で球形に整粒したのち、乾燥すればよい。
In order to obtain the above-mentioned silver oxide granules used in the present invention, for example, silver oxide powder having a normal particle size of 0.1 to 10 μs go # is made into a slurry with water and granulated with a granulator, preferably into spherical particles. It can be sized into spheres using a machine and then dried.

本発明において酸化銀顆粒の粒径を符に50〜500μ
mとしたのは、粒径がそれより小さくなると流動性が低
下し、それに伴なって秤量性、成形性が低下し、逆に粒
径が前記範囲より大きくなると、光*−が少ない薄形電
池では顆粒1個の充填tK与える影響が大きくなり、光
填電にバラツキが発生しやすくなるからである。
In the present invention, the particle size of silver oxide granules is 50 to 500μ.
m is chosen because if the particle size is smaller than this, the fluidity will decrease, and weighability and moldability will decrease accordingly, and conversely, if the particle size is larger than the above range, it will be thin with less light *-. This is because, in a battery, the influence of the filling tK of one granule becomes large, and variations in light charging tend to occur.

カサ密度は成形性に影響を与え、カサ密度がある程度高
いものほど加圧成形による粒子間の結合が強くなり成形
性が向上するが、高すき′ると個々の粒子が圧縮されに
くくなるため、かえって成形性が低下する。そしてカサ
密度は粒径と関連性を有しており、前記範囲内では粒径
が大きいものほどカサ密度が尚い。
Bulk density affects moldability, and the higher the bulk density to some extent, the stronger the bond between particles during pressure molding and the better the moldability, but if the gap is high, it becomes difficult for individual particles to be compressed. On the contrary, the moldability deteriorates. The bulk density has a relationship with the particle size, and within the above range, the larger the particle size, the better the bulk density.

本発明にお・いては、酸化銀を顆粒化することにより、
t&動性を大巾に改良できるので、りん状黒鉛の添加敏
を少なくすることができ、りん状黒鉛をまつ走く使用し
なくてもマス切りによる$?量が可能であり、かつ加圧
成形も充分に行ないうるが、りん状黒鉛を0.05〜2
%(lHiL%、以下同様)程度添加してもよい。
In the present invention, by granulating silver oxide,
Since the t&dynamics can be greatly improved, the addition sensitivity of phosphorous graphite can be reduced, and the cost of mass cutting can be reduced without using a large amount of phosphorous graphite. Although the amount of phosphoric graphite can be reduced to 0.05 to 2
% (lHiL%, hereinafter the same) may be added.

つぎの第1表は酸化銀(*g2o、以下一様)の粒径と
秤量性との関係を示すもので、各種粒径の酸化銀をマス
切シ方式で2004秤量する際のバラツキを調べた結果
を示すものである。
The following Table 1 shows the relationship between the particle size of silver oxide (*g2o, hereinafter referred to as the same) and weighability.We investigated the variation when weighing silver oxide of various particle sizes using the mass cutting method in 2004. The results are shown below.

第   1   表 第1図は酸化銀の粒径とカサ密度との関係を示す−でめ
シ、第2図は各種粒径の酸化銀を51/aI2で直径9
m、厚さ0.5 mに加圧成形した際の割れや欠けKよ
る不良発生率を調べた結果を示すものである0第1表な
らびに第1〜2図に示す結果より明らかなように1粒径
50〜500μmの範囲、カサ密度り、5〜g、5jl
/2−の範囲で秤量値のバラツキが少なく、かつ成形不
良の発生が少ない。
Table 1 Figure 1 shows the relationship between silver oxide particle size and bulk density. Figure 2 shows the relationship between silver oxide particle size and bulk density.
This shows the results of investigating the incidence of defects due to cracking and chipping K when pressure-forming to a thickness of 0.5 m.0 As is clear from the results shown in Table 1 and Figures 1 and 2. 1 particle size range from 50 to 500 μm, bulk density, 5 to g, 5jl
Within the range of /2-, there is little variation in the weighing value, and there is little occurrence of molding defects.

゛錦2表は正極活物質として平均粒径100μ簿の酸化
銀顆粒を用いた本発明の電@Aと正極活物質として平均
粒径5μmの酸化銀粉末を用いた従来電池Bの放電容t
を示すものである。
Table 2 shows the discharge capacity t of the battery @A of the present invention using silver oxide granules with an average particle size of 100 μm as the positive electrode active material and the conventional battery B using silver oxide powder with an average particle size of 5 μm as the positive electrode active material.
This shows that.

電池Aは前記酸化銀顆粒100部(3[蓋部、以下同様
)をマス切シ方式で200jlFff量し、5 L/c
x2で直径9sm、厚さ0.5 Mに加圧成形し、それ
を正極として1taに組み込んだものでめる。一方、電
池Bは前記酸化銀粉末95部とシん状黒鉛5部とを混合
し、マス切シ方式で1701秤量し、61/32で直径
9aI、厚さ0.5 mに加圧成坤し、それを正極とし
て電池に組み込んだものである。
For battery A, 100 parts of the silver oxide granules (3 lid parts, the same shall apply hereinafter) were cut into 200 jlFff using a mass cutting method, and the amount was 5 L/c.
x2 was pressure-molded to a diameter of 9 sm and a thickness of 0.5 M, and this was assembled into a 1 ta as a positive electrode. On the other hand, for battery B, 95 parts of the silver oxide powder and 5 parts of cylindrical graphite were mixed, weighed to 1,701 mm using a mass cutting method, and pressed to a diameter of 9 aI and a thickness of 0.5 m using 61/32. , which was incorporated into a battery as a positive electrode.

電池はいずれも第3図に示すような構成からなる直径9
.5 m、厚さ2Mのボタン形電池であり、第8図にお
いて、(1)は前記のごとき正極、(2)は正極缶、(
3)はセパレータ、(4)は、電解f&吸収体、(5)
はアマルガム化亜鉛を活物質とする負極であシ、電池A
では55岬のアマルガム化亜鉛が用いられ、電fiBで
は444のアマルガム化亜鉛が用いられている・(6)
は負極端子板、(7)は環状ガスケットである0そして
、電解液としては酸化亜鉛を溶解させたs5嘩水酸化カ
リウム水溶液が使用され、放電容量は両電池とも100
個ずつ20℃、22にΩで終止電圧1.2vtで連続放
電させて測定したものである@第   2   表 本発明の電池では、iE極のバラツキが少ないので、亜
鉛量を多くすることができ、その結果、第2表に示すよ
うに放電容量が従来電池に比べて約26s向上し九〇
Each battery has a diameter of 9 and has the configuration shown in Figure 3.
.. It is a button type battery with a length of 5 m and a thickness of 2 M, and in Fig. 8, (1) is the positive electrode as described above, (2) is the positive electrode can, (
3) is a separator, (4) is an electrolytic f & absorber, (5)
is a negative electrode with amalgamated zinc as the active material, battery A
55 Cape amalgamated zinc is used, and DenfiB uses 444 amalgamated zinc (6)
is the negative electrode terminal plate, (7) is the annular gasket, and as the electrolyte, S5 potassium hydroxide aqueous solution in which zinc oxide is dissolved is used, and the discharge capacity of both batteries is 100
Measurements were made by continuously discharging each battery at 20°C, 22 ohms, and a final voltage of 1.2 volts. As a result, as shown in Table 2, the discharge capacity is improved by approximately 26 seconds compared to conventional batteries, resulting in a battery life of 90 seconds.

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

1111図は酸化銀の粒径とカサ密度との関係を示す図
、第2図は酸化銀の粒径と加圧成形時の不良発生率との
関係を示す図、@8図は本発明の酸化銀電池の一実施例
を示す断面歯である0(1)−1,正極 特許出願人   日立マクセル株式会社tJ1図 赦イ乙報ハ肢t(Pfn−) G虹化虚隻の米た窪L%−
Figure 1111 is a diagram showing the relationship between the grain size of silver oxide and bulk density, Figure 2 is a diagram showing the relationship between the grain size of silver oxide and the failure rate during pressure molding, and Figure @8 is a diagram showing the relationship between the grain size of silver oxide and the bulk density. 0(1)-1, which is a cross-sectional tooth showing an example of a silver oxide battery, positive electrode patent applicant Hitachi Maxell Co., Ltd. L%-

Claims (1)

【特許請求の範囲】[Claims] 1、粒径5G〜50(9m、カサ密度1.5〜8.51
/lx2の酸化銀顆粒を正極活物質として用いたことを
特徴とする酸化銀電池0
1. Particle size 5G~50 (9m, bulk density 1.5~8.51
Silver oxide battery 0 characterized by using silver oxide granules of /lx2 as a positive electrode active material
JP56148301A 1981-09-19 1981-09-19 Silver-oxide battery Pending JPS5851477A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56148301A JPS5851477A (en) 1981-09-19 1981-09-19 Silver-oxide battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56148301A JPS5851477A (en) 1981-09-19 1981-09-19 Silver-oxide battery

Publications (1)

Publication Number Publication Date
JPS5851477A true JPS5851477A (en) 1983-03-26

Family

ID=15449714

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56148301A Pending JPS5851477A (en) 1981-09-19 1981-09-19 Silver-oxide battery

Country Status (1)

Country Link
JP (1) JPS5851477A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6030600A (en) * 1996-11-08 2000-02-29 Dowa Mining Co., Ltd. Silver oxide for use in cells and a process for producing the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS565322A (en) * 1979-06-27 1981-01-20 Mitsui Mining & Smelting Co Ltd Preparing granule type silver oxide or silver peroxide
JPS5650062A (en) * 1979-09-28 1981-05-07 Toshiba Battery Co Ltd Alkaline battery

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS565322A (en) * 1979-06-27 1981-01-20 Mitsui Mining & Smelting Co Ltd Preparing granule type silver oxide or silver peroxide
JPS5650062A (en) * 1979-09-28 1981-05-07 Toshiba Battery Co Ltd Alkaline battery

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6030600A (en) * 1996-11-08 2000-02-29 Dowa Mining Co., Ltd. Silver oxide for use in cells and a process for producing the same
US6086845A (en) * 1996-11-08 2000-07-11 Dowa Mining Co., Ltd. Silver oxide for use in cells and a process for producing the same

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