JPS58163168A - Silver oxide cell - Google Patents

Silver oxide cell

Info

Publication number
JPS58163168A
JPS58163168A JP4527282A JP4527282A JPS58163168A JP S58163168 A JPS58163168 A JP S58163168A JP 4527282 A JP4527282 A JP 4527282A JP 4527282 A JP4527282 A JP 4527282A JP S58163168 A JPS58163168 A JP S58163168A
Authority
JP
Japan
Prior art keywords
silver oxide
manganese dioxide
phosphorous graphite
silver
graphite
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.)
Granted
Application number
JP4527282A
Other languages
Japanese (ja)
Other versions
JPH0324740B2 (en
Inventor
Akio Yamamoto
山本 昭雄
Kimitaka Koseki
小関 公崇
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 JP4527282A priority Critical patent/JPS58163168A/en
Publication of JPS58163168A publication Critical patent/JPS58163168A/en
Publication of JPH0324740B2 publication Critical patent/JPH0324740B2/ja
Granted 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

Abstract

PURPOSE:To keep down the internal resistance up to being as low as capable of taking in a discharge reaction without making all processes unnecessary for forming a silver layer on a silver oxide surface by the way of preliminary discharge, by containing phosphorous graphite in a sticking layer of manganese dioxide covering the silver oxide. CONSTITUTION:Positive pole black mixture 1 is made up in the following process that silver oxide powder is granulated into 100-300mu or so in advance while a manganese dioxide or about 2-20mu and phosphorous graphite both are mixed with this granulated powder, and at the time of this mixing, each surface of the said silver oxide granule is layered by dint of the moisture absorption and water absorbability of the manganese dioxide. This black mixture is press- molded into the specified thickness by means of a routine process but even after molding, the sticking layer of said manganese dioxide and phosphorous graphite remains kept intact. The amount of the manganese dioxide used is set at 2-7pts.wt. to 100pts.wt. of the silver oxide while the amount of the phosphorous graphite used is set at 0.2-1pts.wt. to 100pts.wt. in total of the silver oxide and the manganese dioxide, respectively.

Description

【発明の詳細な説明】 この発明は酸化銀を主たる陽極活物質としこれに少量の
二酸化マンガンとりん状黒鉛とを加えた酸化銀電池に関
する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a silver oxide battery in which silver oxide is used as the main anode active material and a small amount of manganese dioxide and phosphorous graphite are added thereto.

酸化銀電池では、陽極活物質としての酸化銀に少量の二
酸化マンガンやりん状黒鉛を配合することがよく行なわ
れている。りん状黒鉛は電子伝導性を助け、また二酸化
マンガンを加えると、放電圧の高い酸化銀と放電圧の低
い二酸化マンガンとの電位差により、電池寿命を事前に
キャッチできるなどの利点が得られるからである。
In silver oxide batteries, it is common practice to mix a small amount of manganese dioxide or phosphorous graphite with silver oxide as the positive electrode active material. Phosphorous graphite helps with electronic conductivity, and adding manganese dioxide has the advantage of being able to predict battery life in advance due to the potential difference between silver oxide, which has a high discharge voltage, and manganese dioxide, which has a low discharge voltage. be.

ところで、このような混合陽極を得る場合、一般には、
酸化銀と二酸化マンガンなどとを粉末状で混合し、これ
を加圧成形する方法がとられるが、粉末混合物では成形
しにくい欠点があり、成形できたとしても充分な強度を
持たせにくい。そこで、」1記混合物を顆粒状とし、こ
れを加圧成形に供することが試みられたが、この方法で
も満足できる成形性は得られなかった。この理由は、二
酸化マンガンがそれ自体ポーラスで水分を吸収しやすい
ものであるため、これを酸化銀と混合して顆粒状として
も、水分吸収によって顆粒状態での強度を充分に保ちに
くいためである。
By the way, when obtaining such a mixed anode, generally,
A method of mixing silver oxide, manganese dioxide, etc. in powder form and press-molding this is used, but a powder mixture has the disadvantage that it is difficult to mold, and even if it can be molded, it is difficult to provide sufficient strength. Therefore, an attempt was made to make the mixture described in item 1 into granules and subject them to pressure molding, but even with this method, satisfactory moldability could not be obtained. The reason for this is that manganese dioxide itself is porous and easily absorbs water, so even if it is mixed with silver oxide and made into granules, it is difficult to maintain sufficient strength in the granule state due to water absorption. .

この発明者らは、かかる観点から鋭意検討した結果、酸
化銀と二酸化マンガンおよびりん状黒鉛とを粉末状で混
合するのではなく、まず酸化銀だけを顆粒状となしこれ
に微粉末状の二酸化マンガンとりん状黒鉛を混合させる
ようにしたところ、顆粒状酸化銀の表面に上記二酸化マ
ンガンとりん状黒鉛とが付着し水分吸収によって容易に
層形成されて、強度的安定な顆粒状陽極合剤となりうる
ことを知り、この発明を完成するに至ったものである。
As a result of intensive studies from this point of view, the inventors of the present invention did not mix silver oxide, manganese dioxide, and phosphorous graphite in powder form, but first made only silver oxide into granules, and then added finely powdered carbon dioxide. When manganese and phosphorous graphite were mixed, the manganese dioxide and phosphorous graphite adhered to the surface of the granular silver oxide and were easily formed into a layer by moisture absorption, resulting in a granular anode mixture with stable strength. Knowing that this could be the case led us to complete this invention.

以下に、この発明の一実施例を図面を参考にして説明す
る。
An embodiment of the present invention will be described below with reference to the drawings.

第1図はこの発明の酸化銀電池の一例を示したもので、
1は陽極合剤、2はアマルガム化した亜鉛粉などを活物
質とした陰極剤、3は上記陰極剤2に接触するビニロン
−レーヨン混抄紙や不織布の如き電解液吸収体、4は上
記吸収体3と上記陽極合剤1との間に介装されるセロハ
ンと微孔性ポリプロピレンフィルムないしポリエチレン
グラフトa合フィルムなどとからなるセパレータである
Figure 1 shows an example of the silver oxide battery of this invention.
1 is an anode mixture, 2 is a cathode agent whose active material is amalgamated zinc powder, 3 is an electrolyte absorber such as vinylon-rayon mixed paper or nonwoven fabric, which is in contact with the cathode agent 2, and 4 is the above absorber. 3 and the anode mixture 1 is a separator made of cellophane and a microporous polypropylene film or a polyethylene graft a composite film.

5は」−記陽極合剤1、セパレータ4および電解液吸収
体3を内填させた鉄にニッケルメッキを施した如き陽極
缶であり、この缶5の開口部に、陰極剤2が内填された
陰極集電体としての陰極端子板6を、ナイロン、ポリエ
チレン、ポリプロピレンなどの各種樹脂もしくはゴムか
らなる断面り字状の環状ガスケット7を介して嵌合させ
、陽極缶5を内方へ締め付けて電池内部を密閉構造にし
ている。
5 is an anode can made of nickel-plated iron in which an anode mixture 1, a separator 4, and an electrolyte absorber 3 are filled, and the opening of the can 5 is filled with a cathode material 2. The cathode terminal plate 6, which serves as a cathode current collector, is fitted with an annular gasket 7 made of various resins such as nylon, polyethylene, polypropylene, or rubber and having a cross-sectional shape, and the anode can 5 is tightened inward. The inside of the battery has a sealed structure.

上記陽極合剤1は、予め酸化銀粉末を100〜300μ
程度の顆粒状となし、これに2〜20μ程度の二酸化マ
ンガンとりん状黒鉛とを混合して、この混合時に二酸化
マンガンの吸湿、吸水性によって」−記酸化銀顆粒物の
表面に層状に付着させてなるものであり、これを常法に
よって所定厚みに加圧成形するが、この成形後も」1記
二酸化マンガンおよびりん状黒鉛の付着層はそのまま保
持されている。」−記二酸化マンガンの使用量は、酸化
銀100重量部に対して2〜7重量部に、またりん状黒
鉛の使用量は、酸化銀と二酸化マンガンとの合計fit
 100重量部に対して0.2〜1重量部に、それぞれ
設定されている。
The above anode mixture 1 is prepared by adding 100 to 300μ of silver oxide powder in advance.
This is mixed with about 2 to 20 μ of manganese dioxide and phosphorous graphite, and when mixed, due to the hygroscopic and water absorbing properties of manganese dioxide, it is adhered in a layer to the surface of the silver oxide granules. This is pressure-molded to a predetermined thickness by a conventional method, but even after this molding, the adhesion layer of manganese dioxide and phosphorous graphite described in 1. is maintained as it is. -The amount of manganese dioxide to be used is 2 to 7 parts by weight per 100 parts by weight of silver oxide, and the amount of phosphorous graphite to be used is the total fit of silver oxide and manganese dioxide.
The content is set at 0.2 to 1 part by weight per 100 parts by weight.

このように、この発明の酸化銀電池は、陽極合剤を強度
充分な顆粒状となすことができるから、その成形作業性
が大巾に改善されるとともに、酸化銀がこれよりも酸化
力の弱い二酸化マンガンで被覆された構造となっている
ため、セパレータの酸化劣化を抑制できる、二酸化マン
ガン付着層が相互に鎖状につながって放電反応に好結果
を与えるなどのほか、二酸化マンガンの吸湿、吸液性に
起因して重負荷放電特性が大きく改善されるなどの効果
がもたらされる。
As described above, in the silver oxide battery of the present invention, since the anode mixture can be formed into granules with sufficient strength, the molding workability is greatly improved, and the silver oxide has a higher oxidizing power than the granules. Because it has a structure coated with weak manganese dioxide, it can suppress oxidative deterioration of the separator, and the manganese dioxide adhesion layers are connected to each other in a chain form, giving good results to the discharge reaction. Due to its liquid absorption properties, effects such as greatly improved heavy load discharge characteristics are brought about.

第2図は、この発明の酸化第一銀電池につき、」−記の
重負荷放電特性を示したもので、0.025にΩ負荷の
もとての試験結果である。図中、曲線−1は本発明品の
結果、曲線−2は粉末状混合に係る従来品の結果である
。これより、この発明の電池がすぐれた放電性能を有し
ているものであることがわかる。
FIG. 2 shows the heavy load discharge characteristics of the silver oxide battery of the present invention, and shows the test results under a 0.025 Ω load. In the figure, curve 1 is the result of the product of the present invention, and curve 2 is the result of the conventional product related to powder mixture. This shows that the battery of the present invention has excellent discharge performance.

また、この発明の酸化銀電池では、酸化銀を被覆した二
酸化マンガンの付着層中にりん状黒鉛を含ませるように
しているから、この黒鉛を含ませないときは予備放電に
よって酸化銀表面に銀層を形成して内部抵抗を大きく低
下させる必要があったのに対し、かかる処置を一切要す
ることなく前記放電反応に関与させうる低い内部抵抗に
抑えることができる。
In addition, in the silver oxide battery of this invention, phosphorous graphite is included in the adhesion layer of manganese dioxide coated with silver oxide, so if this graphite is not included, the silver oxide surface is coated with silver by preliminary discharge. Whereas it was necessary to greatly reduce the internal resistance by forming a layer, it is possible to suppress the internal resistance to a low level that can participate in the discharge reaction without requiring any such treatment.

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

第1図はこの発明の酸化銀電池の一例を示す断+5+ 
            ’)QA面図、第2図は上記
電池の重負荷放電特性を示す特性図である。 1・・・陽極合剤。 −(6)
Figure 1 shows an example of a silver oxide battery according to the present invention.
') QA surface diagram, FIG. 2 is a characteristic diagram showing the heavy load discharge characteristics of the above battery. 1... Anode mixture. -(6)

Claims (1)

【特許請求の範囲】[Claims] (1)顆粒状とした酸化銀の表面に微粒子状の二酸化マ
ンガンとりん状黒鉛とからなる付着層を設けて陽極合剤
を構成したことを特徴とする酸化銀電池。
(1) A silver oxide battery characterized in that an adhesion layer consisting of particulate manganese dioxide and phosphorous graphite is provided on the surface of granular silver oxide to constitute an anode mixture.
JP4527282A 1982-03-19 1982-03-19 Silver oxide cell Granted JPS58163168A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4527282A JPS58163168A (en) 1982-03-19 1982-03-19 Silver oxide cell

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4527282A JPS58163168A (en) 1982-03-19 1982-03-19 Silver oxide cell

Publications (2)

Publication Number Publication Date
JPS58163168A true JPS58163168A (en) 1983-09-27
JPH0324740B2 JPH0324740B2 (en) 1991-04-04

Family

ID=12714673

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4527282A Granted JPS58163168A (en) 1982-03-19 1982-03-19 Silver oxide cell

Country Status (1)

Country Link
JP (1) JPS58163168A (en)

Cited By (3)

* 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
JP2006252899A (en) * 2005-03-10 2006-09-21 Hitachi Maxell Ltd Silver oxide battery
CN114671455A (en) * 2022-03-03 2022-06-28 先导薄膜材料(广东)有限公司 Method for industrially producing silver oxide for battery

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654760A (en) * 1979-10-09 1981-05-14 Toshiba Battery Co Ltd Manufacture of alkaline battery
JPS579063A (en) * 1980-06-19 1982-01-18 Toshiba Battery Co Ltd Alkaline battery

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5654760A (en) * 1979-10-09 1981-05-14 Toshiba Battery Co Ltd Manufacture of alkaline battery
JPS579063A (en) * 1980-06-19 1982-01-18 Toshiba Battery Co Ltd Alkaline battery

Cited By (5)

* 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
JP2006252899A (en) * 2005-03-10 2006-09-21 Hitachi Maxell Ltd Silver oxide battery
CN114671455A (en) * 2022-03-03 2022-06-28 先导薄膜材料(广东)有限公司 Method for industrially producing silver oxide for battery
CN114671455B (en) * 2022-03-03 2023-10-17 先导薄膜材料(广东)有限公司 Method for industrially producing silver oxide for battery

Also Published As

Publication number Publication date
JPH0324740B2 (en) 1991-04-04

Similar Documents

Publication Publication Date Title
GB2174534A (en) Zinc/air cell cathode
US3573106A (en) Electric battery having a laminated semipermeable barrier/absorbent separator
US3640770A (en) Rechargeable metal halide battery
JPS58163168A (en) Silver oxide cell
US3888700A (en) Absorbent separator for an electric battery
JPS58163151A (en) Silver oxide cell
JPS58163167A (en) Silver oxide cell
GB2084790A (en) Lead-acid batteries
JPH09180708A (en) Alkaline dry cell
US20040005503A1 (en) Nickel-hydrogen storage battery and method for manufacture thereof
JPS6381762A (en) Button type alkaline battery
JPS5830065A (en) Manufacture of button type zinc-air cell
JPS61214362A (en) Alkaline manganese battery
JPS5868878A (en) Organic electrolyte cell
JPS5999671A (en) Silver suboxide battery
JPS5928025B2 (en) Alkaline battery manufacturing method
JPS58163166A (en) Argentic oxide cell
JPS60264049A (en) Alkali zinc battery
JPS5999662A (en) Production method of silver (ii) oxide cell
JPS60241649A (en) Manufacture of alkali-manganese cell
JPH03184257A (en) Battery
JPH09129238A (en) Battery
JPS5931179B2 (en) Zinc alkaline secondary battery
JPS6276251A (en) Air-cell
JPS5893157A (en) Manufacture of button type alkaline cell