JPS6041760A - Mercury battery - Google Patents

Mercury battery

Info

Publication number
JPS6041760A
JPS6041760A JP58149771A JP14977183A JPS6041760A JP S6041760 A JPS6041760 A JP S6041760A JP 58149771 A JP58149771 A JP 58149771A JP 14977183 A JP14977183 A JP 14977183A JP S6041760 A JPS6041760 A JP S6041760A
Authority
JP
Japan
Prior art keywords
oxide
positive
pellet
cadmium oxide
cadmium
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
JP58149771A
Other languages
Japanese (ja)
Inventor
Toshihiko Izumikawa
泉川 敏彦
Keigo Momose
百瀬 敬吾
Haruo Kogure
小暮 春男
Hayashi Hayakawa
早川 林
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP58149771A priority Critical patent/JPS6041760A/en
Publication of JPS6041760A publication Critical patent/JPS6041760A/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
    • 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 provide a mercury battery having steady static performance and discharge capacity by adding a specivied amount of cadmium oxide to a positive mix containing mercuric oxide as main positive active material. CONSTITUTION:1-8pts.wt. cadmium oxide is added to 100pts.wt. mercuric oxide in a positive mix using mercuric oxide as main positive active material. For example, a positive mix 2 is formed in such a manner that 5pts.wt. graphite or acetylene black and 1-5pts.wt. cadmium oxide are mixed to 100pts.wt. mercuric oxide, and the mixture is formed in a form of pellet, then the pellet is pressed in a positive case with a positive ring 3. Since the positive mix containing cadmium oxide is easy to form a pellet, the pellet has uniform density and steady electrolyte absorption amount, and electrolyte penetrates uniformly into the pellet. Since cadmium oxide is converted to cadmium hydroxide by electrolyte, electrolyte penetrates to fine pores of the mix. Therefore, discharge capacity and static performance of a battery are stabilized.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、水銀電池の正極の改良に関するものである。[Detailed description of the invention] Industrial applications The present invention relates to improvements in positive electrodes for mercury batteries.

従来の構成とその問題点 水銀電池は、放電中の電圧変化が少なく、保存性能が優
れており、小形で容積2重は当たりの電気容量が大きい
。また、開路電圧も長期にわたって安定していることか
ら、小形電子機器の電源として、補聴器、カメラの露出
部、開側2に、腕時計。
Conventional configuration and its problems Mercury batteries have little voltage change during discharge, excellent storage performance, are small, and have a large electric capacity per double volume. In addition, since the open circuit voltage is stable over a long period of time, it can be used as a power source for small electronic devices such as hearing aids, exposed parts of cameras, open side 2, and wristwatches.

トランシーバ−、ポケットベル等に1史用されている。It has been used for a long time in transceivers, pagers, etc.

近年、機器の小形化に伴い電池の小形化が要求されてい
る。その結果、電池の放電容量、静特性の安定化が問題
となってきている。
In recent years, as devices have become smaller, there has been a demand for smaller batteries. As a result, stabilization of the discharge capacity and static characteristics of batteries has become a problem.

従来の水銀電池の正極′f:第1図に示す。図中1は正
極端子を兼ねた金属ケース、2はiE極活物質である酸
化水銀、二酸化マンガンと、導電剤である黒鉛又はアセ
チレンブラック、及び焼成マンガンからなる正極合剤を
粗成形した後、正極リング3とともにケースに加圧成形
し、たものである。
A positive electrode 'f of a conventional mercury battery is shown in FIG. In the figure, 1 is a metal case that also serves as a positive electrode terminal, and 2 is a positive electrode mixture consisting of iE electrode active materials mercury oxide and manganese dioxide, conductive agents graphite or acetylene black, and calcined manganese. It is press-molded into a case together with the positive electrode ring 3.

上記の構成では、正極リング下部2aの合剤密度が高く
なり、電解液の浸透が悪くなる不都合がある。丑だ−J
二+4(2合剤組成では、合剤の成形性が小安定で、合
剤重度が不均一となるため、電解液の浸透速度が遅く、
吸液量が安定していない。その結果、電池の放電容量、
静特性が不安定になる。
In the above configuration, there is a disadvantage that the mixture density in the lower part 2a of the positive electrode ring becomes high, and penetration of the electrolyte becomes poor. It's ox-J
2+4 (With the 2 mixture composition, the moldability of the mixture is slightly stable and the mixture density is uneven, so the permeation rate of the electrolyte is slow,
The amount of liquid absorbed is not stable. As a result, the discharge capacity of the battery,
Static characteristics become unstable.

発明の目的 本発明は、上記のような欠点を屓消し、i′rfI特I
I4:、 。
OBJECTS OF THE INVENTION The present invention eliminates the above-mentioned drawbacks and
I4:, .

放電容量の安定した水銀電池を提供することをl」的と
する。
Our objective is to provide a mercury battery with stable discharge capacity.

発明の構成 本発明は、酸化水銀を主なる正極活物質とする正極合剤
中に酸化水銀100重破部に7・Jシて1〜8重濱部の
酸化カドミウムを含治させるものである。
Structure of the Invention The present invention is a positive electrode mixture containing mercury oxide as the main positive electrode active material, in which 1 to 8 layers of cadmium oxide is impregnated by 7 J to 100 layers of mercury oxide. .

この構成によれば、合剤の成形r]−7がよく、成形さ
れた合剤の密度が均一になる。傷に1に極すングF台(
(2aの合剤密度が電解液を吸液し2ないほど高くなら
ないため、正極合剤中へ迅速にかつ均−Vこ吸液され、
吸液量も安定する。また、IE正極合剤中ことによって
、さらに電lIJイ液が雅1113\侵透していく効果
がある。その結果、放′11容吊、静特性が安定する。
According to this configuration, the molding of the mixture r]-7 is good and the density of the molded mixture becomes uniform. It is extremely effective against scratches.
(Since the density of the mixture 2a does not become so high that it absorbs the electrolyte, it is quickly and evenly absorbed into the positive electrode mixture,
The amount of liquid absorbed is also stable. Moreover, depending on the IE positive electrode mixture, there is an effect that the electrolyte liquid further penetrates into the IE cathode mixture. As a result, the suspension and static characteristics become stable.

また、酸化カドミウムは、負極側から発生する水素ガス
を除去するため、′電池の膨張寸/こけ破裂による機器
の破損を防1」−するという利点もある。
Furthermore, since cadmium oxide removes hydrogen gas generated from the negative electrode side, it also has the advantage of preventing equipment damage due to battery expansion/molten rupture.

実施例の説明 第2図は本発明の実施例による水銀電池MR9を示す。Description of examples FIG. 2 shows a mercury cell MR9 according to an embodiment of the invention.

図において、1は厚さ0.30団の鋼板を段付部下部外
径13.1 mrn 、段付部下gB 2.60 mm
 r段付部下部外径15.6 mm 、高さ6.80 
mmに1Jち抜き加工し、二ノク−ルメノキをh布し7
たj、F 4會ケースである。2け正極合剤で、活物質
である酸化水銀100重は部に導電性吻t4である黒鉛
ま/こはアセチレンプラック5ノロ計部、酸化カドミウ
ムを1〜5重量部を混合し、ペレット状に成形した後、
正極リング3とともにIE極ケースに加圧成形したもの
である。41j上ポリエチレン、ポリプロピレンなどよ
りなるセパレータ、5dアルカリ′fi +性液を含ん
だセロース系の含液拐である。6幻−負極合剤で、汞化
率5〜15係の水化亜鉛粉末と電M’(液の水酸化カリ
ウム水溶液ど増粘剤のポリアクリル酸ソーダやカルボギ
ンメチルセルロース等との混練物よりなる。7は]1ノ
、さ0.40 +rtynのニッケルーステンレス鋼−
鋼の三層クラッド祠を外径13.80 mm 、高さ2
.60mmに加工し7た封口板、8Cポリアミド樹脂、
ポリエチI/ノ樹脂、ボリグロピレン4fg Ile 
等J:りなる絶縁ガスヶ、)・であり、このガスケツ)
・8を装着した組立封1」板7内に前記の負極が充填σ
れる。
In the figure, 1 is a steel plate with a thickness of 0.30 mm, the outer diameter of the lower part of the stepped part is 13.1 mrn, and the lower part of the stepped part gB is 2.60 mm.
r Stepped part lower part outer diameter 15.6 mm, height 6.80
Punch out 1J to mm, and cloth 7
This is the F4 case. In a 2-piece positive electrode mixture, 100 parts by weight of mercury oxide as an active material, 5 parts by weight of graphite or acetylene plaque as a conductive material, and 1 to 5 parts by weight of cadmium oxide were mixed, and the mixture was made into pellets. After forming into
It is press-molded into the IE electrode case together with the positive electrode ring 3. 41j is a separator made of polyethylene, polypropylene, etc.; 6 Phantom-negative electrode mixture, from a kneading product of zinc hydrate powder with a concentration of 5 to 15 and electrolytic M' (liquid potassium hydroxide aqueous solution, thickeners such as sodium polyacrylate and carbogine methylcellulose). 7 is] 1 no, 0.40 +rtyn nickel-stainless steel-
A three-layer steel clad shrine with an outer diameter of 13.80 mm and a height of 2
.. Sealing plate processed to 60mm, 8C polyamide resin,
Polyethylene I/resin, polyglopylene 4fg Ile
Etc. J: Rinaru insulating gas gasket, ), and this gasket)
・The above-mentioned negative electrode is filled in the assembly seal 1'' plate 7 with 8 attached.
It will be done.

酸化カドミウムを含有した正極合剤は、成形性か摩れて
いるため、加圧成形される際に合剤密度か均一になり、
電解液の吸液量が安定し、さらに合剤へ均一に電解液が
浸透する。また、酸化カドミウムは、電解液中で水酸化
カドミウムに変化することによ−)で、きらに合剤+1
i111部へ電Jqq液が浸透していく。その結果、電
池の放電容量と静特性が安定する。
Since the positive electrode mixture containing cadmium oxide has poor moldability, the density of the mixture becomes uniform when it is pressure-molded.
The amount of electrolyte absorbed is stabilized, and the electrolyte permeates uniformly into the mixture. In addition, cadmium oxide changes to cadmium hydroxide in the electrolyte solution, resulting in a mixture of +1
The electric Jqq liquid penetrates into the i111 part. As a result, the discharge capacity and static characteristics of the battery are stabilized.

第3図は正極合剤の酸化カドミウムの含有割合を変えた
電池についての電池内部抵抗のバラツキと平均値の関係
を示している。なお、試料数は各々20個である。酸化
カドミウムの含有、1111合を酸化水銀100重量部
に対して1〜8重石部にした際に内部抵抗が安定し、バ
ラツキが小さくな−)ている。
FIG. 3 shows the relationship between the variation in battery internal resistance and the average value for batteries in which the content of cadmium oxide in the positive electrode mixture was changed. Note that the number of samples was 20 for each. When the content of cadmium oxide is 1 to 8 parts by weight per 100 parts by weight of mercury oxide, the internal resistance becomes stable and the variation becomes small.

ま/ζ、第4図は酸化カドミウムの介イ〕−9U合と放
電g解のバラツキと平均値の関係を示している。
Fig. 4 shows the relationship between the dispersion of the discharge g-solution and the average value for the cadmium oxide intercalation [-9U].

この図より、明らかに酸化水銀100徂搦一部に対して
酸化カドミウムを1〜8重量部含有する際に放電容量が
安定し、バラツギが小さくなっている。
From this figure, it is clear that when 1 to 8 parts by weight of cadmium oxide is contained per 100 parts of mercury oxide, the discharge capacity becomes stable and the variation becomes small.

次に酸化水銀100車量部に対して酸化カドミウム3型
取部を含有する正極合剤を用いた′ε池をA1酸化カド
ミウムを含まない正極合剤を用いた電池をBとして、内
部抵抗、放電容量の標準偏差を比較してみると、次表の
とおりである。なお、試料数に各201161 テある
Next, a battery using a positive electrode mixture containing 3 molded portions of cadmium oxide with respect to 100 parts by weight of mercury oxide is designated A1, a battery using a positive electrode mixture containing no cadmium oxide is designated B, and the internal resistance, A comparison of the standard deviations of discharge capacity is shown in the following table. There are 201,161 samples each.

発明の効果 以上の実施+71Jからも明ら刀・の」、うに、本発明
によれば、容昂、静肪性か安定した水銀電池が得しれる
It is clear from the implementation of the invention that exceeds the effects of the invention.According to the present invention, a mercury battery that is both accommodating and statically stable can be obtained.

4、図面の簡t1jな+ife IJ 第1図は従来構成による正極ケースに正極合剤を充填し
た状態を示す縦断18」図、第2図−木兄1,1l−1
の実施例(fこおける′電池の一部を断面Vこした側面
図、第3図は合剤の酸化カドミウムの含有A11合を変
1);させた際の内部抵抗の推移を示す図、均′54図
を」、酸化カドミウムの含有割合を変化させた際の放電
容量の推移を示す図である。
4. Simplification of the drawings Figure 1 is a vertical cross-section 18'' showing the state in which the positive electrode case is filled with the positive electrode mixture according to the conventional configuration, Figure 2 - Kinoi 1, 1l-1
Example (a side view of a part of the battery in section V, with the cross section V cut out; Figure 3 shows the change in internal resistance when the content of cadmium oxide in the mixture is changed to 1); 54 is a diagram showing the transition of discharge capacity when the content ratio of cadmium oxide is changed.

1・・・正イ愼ケース、2 ・ 正極合剤、4 セパレ
ータ、5 ・・・含液材、6・・ ・負極、7− 封1
」板、8・・・・・絶縁力スケット。
1...Positive case, 2-Positive electrode mixture, 4 Separator, 5...Liquid-containing material, 6...-Negative electrode, 7- Seal 1
” Board, 8... Insulation power socket.

代理人の氏名 弁μ]!士 中 尾 敏 男 ほか1名
車 1 1] 第2図 第3図 部 抵 抗lO :■
Agent's name Benmu]! Toshio Nakao and 1 other car 1 1] Figure 2 Figure 3 Part Resistance lO: ■

Claims (1)

【特許請求の範囲】[Claims] 主なる正極活物質として酸化水銀を1史用する正極合剤
中に酸化水銀100重量部に灯して1〜8重量部の酸化
カドミウムを含有させたことを特徴とする水銀電池。
A mercury battery characterized in that a positive electrode mixture containing mercury oxide as a main positive electrode active material contains 1 to 8 parts by weight of cadmium oxide in addition to 100 parts by weight of mercury oxide.
JP58149771A 1983-08-17 1983-08-17 Mercury battery Pending JPS6041760A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58149771A JPS6041760A (en) 1983-08-17 1983-08-17 Mercury battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58149771A JPS6041760A (en) 1983-08-17 1983-08-17 Mercury battery

Publications (1)

Publication Number Publication Date
JPS6041760A true JPS6041760A (en) 1985-03-05

Family

ID=15482371

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58149771A Pending JPS6041760A (en) 1983-08-17 1983-08-17 Mercury battery

Country Status (1)

Country Link
JP (1) JPS6041760A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04129019U (en) * 1991-05-10 1992-11-25 株式会社三宝商会 Steel panels for hot water floor heating

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04129019U (en) * 1991-05-10 1992-11-25 株式会社三宝商会 Steel panels for hot water floor heating

Similar Documents

Publication Publication Date Title
US3457112A (en) Lead-acid storage battery
US3870564A (en) Alkaline cell
US2542710A (en) Alkaline dry cell
US3960600A (en) Anode construction
JPS6041760A (en) Mercury battery
US2692215A (en) Alkaline dry cell
US2542575A (en) Alkaline dry cell
JPS618852A (en) Nonaqueous electrolyte cell
JPS63232266A (en) Alkaline dry battery
JPH0212762A (en) Silver oxide battery
EP4131530A1 (en) Flat battery and method for manufacturing same
JPS59128772A (en) Nonaqueous solvent battery
JPS59101772A (en) Silver oxide battery
JPS61284061A (en) Organic electrolyte battery
JPS5999662A (en) Production method of silver (ii) oxide cell
JPS59224058A (en) Alkaline battery
JPS58197675A (en) Alkaline cell
JPS63164162A (en) Cadmium negative electrode for alkaline storage battery
JPH0570265B2 (en)
JPH0773047B2 (en) Negative electrode for sealed alkaline storage battery
JPS60124355A (en) Lithium battery
JPS5889775A (en) Closed alkaline cell
JPS5999671A (en) Silver suboxide battery
JPS58108659A (en) Manufacture of electrode for lead battery
JPS585965A (en) Alkaline battery