JPS60158554A - Alkaline battery - Google Patents

Alkaline battery

Info

Publication number
JPS60158554A
JPS60158554A JP59016624A JP1662484A JPS60158554A JP S60158554 A JPS60158554 A JP S60158554A JP 59016624 A JP59016624 A JP 59016624A JP 1662484 A JP1662484 A JP 1662484A JP S60158554 A JPS60158554 A JP S60158554A
Authority
JP
Japan
Prior art keywords
zinc
mercury
thallium
added
alloy
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
JP59016624A
Other languages
Japanese (ja)
Inventor
Konosuke Ikeda
宏之助 池田
Satoshi Ubukawa
生川 訓
Mutsumi Yano
睦 矢野
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.)
Sanyo Electric Co Ltd
Sanyo Denki Co Ltd
Original Assignee
Sanyo Electric Co Ltd
Sanyo Denki 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 Sanyo Electric Co Ltd, Sanyo Denki Co Ltd filed Critical Sanyo Electric Co Ltd
Priority to JP59016624A priority Critical patent/JPS60158554A/en
Publication of JPS60158554A publication Critical patent/JPS60158554A/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
    • H01M4/38Selection of substances as active materials, active masses, active liquids of elements or alloys
    • H01M4/42Alloys based on zinc
    • 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)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Primary Cells (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

PURPOSE:To reduce the amount of mercury to be added to zinc by using zinc- thallium-mercury alloy and alkaline electrolyte prepared by dissolving a specified amount of zinc oxide. CONSTITUTION:A zinc-thallium-mercury alloy anode and alkaline electrolyte containing 1-7% zinc oxide are used. For example, monothallium nitrate is dissolved in water, then zinc powder is added in the solution and stirred. The solution is filtered out and zinc-thallium alloy obtained are dried at 70 deg.C. The zinc- thallium alloy is added into potassium hydroxide solution, then mercury is added to it, and they are stirred and filtered and washed until the pH of the filtrate becomes about 7. The alloy powder is dried under reduced pressure at 40 deg.C. Zinc-thallium-mercury alloy powder having a amalgamation ratio of 0.5% is obtained.

Description

【発明の詳細な説明】 (イ) 産業上の利用分野 本発明は亜鉛を陰極活物質とするアルカリ電池に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application The present invention relates to an alkaline battery using zinc as a cathode active material.

(ロ)従来技術 この種電池区二おいては、陰極活物質としての亜鉛がア
ルカリ電解液中1二存在すると水素発生を伴いながら溶
解し、これが陰極の自己放電孟二つながって保存性能を
劣下させると共に電池内部圧の上昇によって漏液現象を
招くという不都合がある。
(b) Conventional technology In this type of battery, when zinc as a cathode active material is present in an alkaline electrolyte, it dissolves with hydrogen generation, which leads to self-discharge of the cathode and deteriorates storage performance. There is an inconvenience that as the internal pressure of the battery decreases, the internal pressure of the battery increases, causing a leakage phenomenon.

このような不都合を防止するためC:陰極活物質として
水化した亜鉛粉末が一般I:用いられている。
In order to prevent such inconveniences, C: hydrated zinc powder is generally used as the cathode active material.

しかしながら、水銀は人体に極めて有害な物質であるの
で水銀を電池区二使用することは大きな社会問題となっ
ている。
However, since mercury is an extremely harmful substance to the human body, the use of mercury in batteries has become a major social problem.

そのため、水銀の添加量を減じる目的で種々の添加剤を
加える提案がなされている。例えば特公昭55−133
86号公報I:よれば1通常水銀の添加量1d8〜15
%であったが腐食防止剤を添加すれば水銀の添加量を5
%以下(具体例として3〜5%)に減じることが可能で
ある旨の開示がある。
Therefore, proposals have been made to add various additives for the purpose of reducing the amount of mercury added. For example, the special public service 133-1973
No. 86 Publication I: According to 1, the amount of added mercury is usually 1d8 to 15
%, but if a corrosion inhibitor is added, the amount of mercury added can be reduced to 5%.
There is a disclosure that it is possible to reduce the amount to % or less (3 to 5% as a specific example).

しQ 発明の目的 本発明の目的とするところは、氷化亜鉛への添加剤を追
究すると共にアルカリ電解液中の酸化亜鉛濃度1二よる
依存性全考慮し、水銀添加量を激減させることにある゛
Q. Purpose of the Invention The purpose of the present invention is to investigate additives to frozen zinc, and to drastically reduce the amount of mercury added by taking into account the dependence of the zinc oxide concentration in the alkaline electrolyte. There is.

四 発明の構成 本発明は陽極と、亜鉛−タリウム−水銀合金を活物質と
する陰極と、酸化亜鉛を1〜7%溶解したアルカリ電解
液とを備えたアルカリ電池にある。
4. Structure of the Invention The present invention resides in an alkaline battery comprising an anode, a cathode containing a zinc-thallium-mercury alloy as an active material, and an alkaline electrolyte in which 1 to 7% of zinc oxide is dissolved.

匝)実施例 水500 meに硝酸第1タリウム5.0yを添加し攪
拌溶解させた後、亜鉛粉末500 ff加え10分間よ
く攪拌を行い、その後溶液を口過して得られた亜鉛−タ
リウム合金粉末=l(70″Cで乾燥する。
Example: After adding 5.0 y of thallium nitrate to 500 ml of water and stirring to dissolve it, 500 ff of zinc powder was added and stirred well for 10 minutes, and then the solution was passed through the mouth to obtain a zinc-thallium alloy. Powder = l (dry at 70″C.

乾燥後、この亜鉛−タリウム合金粉末’f 500 m
eの20重口%水酸化カリウム水溶液に添加すると共に
水銀2.5yを添加し30分間よく攪拌したのち溶液を
口過し、ついで口過液のP Hが約7になるまで水で洗
浄する。その後40°Cで真空乾燥して陰極活物′にと
しての亜鉛−タリウム−水銀合金粉末(汞化率0.5%
)を得る。
After drying, this zinc-thallium alloy powder'f 500 m
Add 2.5y of mercury to a 20% by weight aqueous potassium hydroxide solution of e, stir well for 30 minutes, pass through the solution, and then wash with water until the pH of the passthrough becomes approximately 7. . After that, it was dried under vacuum at 40°C and used as a zinc-thallium-mercury alloy powder (with a hydrogenation rate of 0.5%) as a cathode active material.
).

又、40重量%水酸化カリウム水溶液を80°Cまで昇
温させた後、酸化亜鉛を濃度で1%、5%及び7%g二
なるよう孟二添力vし溶解させて本発明のアルカリ電解
液を得る。
In addition, after raising the temperature of a 40% by weight aqueous potassium hydroxide solution to 80°C, zinc oxide was added to the solution to give a concentration of 1%, 5%, and 7% g, and dissolved to form the alkali of the present invention. Obtain electrolyte.

一方、比較のため従来より用いられている水化亜鉛(氷
化率1.5%、6.0%、lO%)及び40重口%水酸
化カリウム水溶液に酸化亜鉛t−飽和溶解させたアルカ
リ電解液全作成した。
On the other hand, for comparison, the conventionally used zinc hydrate (freezing rate: 1.5%, 6.0%, lO%) and the alkali solution containing zinc oxide t-saturated in a 40% by weight potassium hydroxide aqueous solution. All electrolytes were prepared.

第1表は亜鉛−タリウム−水銀合金粉末と氷化亜鉛粉末
とを夫々一定量取出し、これ全酸化亜鉛濃度が異なる種
々のアルカリ電解液中に浸漬し。
Table 1 shows that certain amounts of zinc-thallium-mercury alloy powder and frozen zinc powder were taken out and immersed in various alkaline electrolytes having different total zinc oxide concentrations.

温度45°Cで6日間放置した際のガス発生量を比較し
たものである。
This is a comparison of the amount of gas generated when the samples were left at a temperature of 45°C for 6 days.

父、典2表は亜鉛−タリウムー水銀合金粉末或いは氷化
亜鉛粉末を夫々活物質とする陰極と、二酸化マンガンを
活物質とする陽極と、酸化亜鉛濃度が異なる種々の水酸
化カリウム水溶液よりなるアルカリ′屯解液とを用いて
夫々100個のアルカリ電池を作成し、温I!t6D℃
、湿度90%で放置し6ケ月後の漏液個数を調べた結果
を示す。
Table 2 shows a cathode made of zinc-thallium-mercury alloy powder or frozen zinc powder as an active material, an anode made of manganese dioxide as an active material, and an alkali made of various potassium hydroxide aqueous solutions with different concentrations of zinc oxide. 100 alkaline batteries were made using each of the ``Tunkai solution'' and warmed up. t6D℃
, shows the results of examining the number of leaks after 6 months of being left at 90% humidity.

第1表 第 2 表 ) 】 ) ) ) 第1表及び第2表から明らかなよう(=、氷化亜鉛はそ
の氷化率が大孟二なるほどガス発生量が減少し、又漏液
現象が抑制されるのがわかる。更にガス発生量及び漏液
現象は電解液中の酸化亜鉛濃度(:も影響をうけること
がわかる。
As is clear from Tables 1 and 2 (Table 1, Table 2), the higher the freezing rate of frozen zinc, the less gas it generates, and the more the leakage phenomenon occurs. It can be seen that the amount of gas generated and the leakage phenomenon are also affected by the concentration of zinc oxide in the electrolyte.

さて1本発明電池のように陰極活物質として亜鉛−タリ
ウム−水銀合金粉末を用い、且酸化亜鉛濃度が1〜7%
のアルカリ電解液を用いた場合には、水銀の添加量ヲ0
.5%としても従来の永イし亜鉛(氷化率7.0%)を
陰極活物質とする場合に比してガス発生量を抑制するこ
とができる。
Now, as in the battery of the present invention, zinc-thallium-mercury alloy powder is used as the cathode active material, and the zinc oxide concentration is 1 to 7%.
When using an alkaline electrolyte, the amount of mercury added is 0.
.. Even if it is 5%, the amount of gas generated can be suppressed compared to the case where conventional long-lived zinc (freezing rate: 7.0%) is used as the cathode active material.

(へ)発明の効果 上述した如(、亜鉛−タリウム−水銀合金を陰極活物質
とし、酸化亜鉛を1〜7%溶解したアルカリ電解液を用
いることにより一従来陰極活物質として用いていた氷化
也鉛(二おける水銀の添加口に対して極少量の水銀を用
いるのみで同等若しくはそれ以上の電池性能を得ること
ができるものであり、その工業的価値は極めて大である
(f) Effects of the invention As mentioned above, by using a zinc-thallium-mercury alloy as a cathode active material and using an alkaline electrolyte in which 1 to 7% of zinc oxide is dissolved, the ice that was conventionally used as a cathode active material is reduced. It is possible to obtain the same or better battery performance by using only a very small amount of mercury in the mercury addition port, and its industrial value is extremely large.

出願人 三洋電機株式会社 代理人 弁理士 佐 野 静 夫Applicant: Sanyo Electric Co., Ltd. Agent: Patent attorney Shizuo Sano

Claims (1)

【特許請求の範囲】[Claims] ■ 陽極と、亜鉛−タリウム−水銀合金全活物質とする
陰極と、酸化亜鉛′t−1〜7%溶解したアルカリ電解
液とを備えたアルカリ電池。
(2) An alkaline battery comprising an anode, a cathode made entirely of a zinc-thallium-mercury alloy active material, and an alkaline electrolyte in which zinc oxide't-1 to 7% is dissolved.
JP59016624A 1984-01-30 1984-01-30 Alkaline battery Pending JPS60158554A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59016624A JPS60158554A (en) 1984-01-30 1984-01-30 Alkaline battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59016624A JPS60158554A (en) 1984-01-30 1984-01-30 Alkaline battery

Publications (1)

Publication Number Publication Date
JPS60158554A true JPS60158554A (en) 1985-08-19

Family

ID=11921496

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59016624A Pending JPS60158554A (en) 1984-01-30 1984-01-30 Alkaline battery

Country Status (1)

Country Link
JP (1) JPS60158554A (en)

Similar Documents

Publication Publication Date Title
JPS58131660A (en) Reducing agent in alkali battery electrolyte
JP2770396B2 (en) Zinc alkaline battery
JPS60158554A (en) Alkaline battery
JPH0371559A (en) Zinc alkaline battery
JPS60158553A (en) Alkaline battery
JP2737233B2 (en) Zinc alkaline battery
JPH0317181B2 (en)
JPS60136182A (en) Air cell
JP2737231B2 (en) Zinc alkaline battery
JPS61181071A (en) Alkaline cell
JPS63254671A (en) Zinc alkaline cell
JP2737232B2 (en) Zinc alkaline battery
CA1133578A (en) Aluminum additive for cells using divalent silver oxide electrodes
JPS63276871A (en) Zinc alkali cell
JPS63248061A (en) Zinc alkaline battery
JPS61118965A (en) Alkaline battery
JPS63248062A (en) Zinc alkaline battery
JPS63248065A (en) Zinc alkaline battery
JPS6113580A (en) Air cell
JPH02174067A (en) Alkaline battery
JPS63248063A (en) Zinc alkaline battery
JPS63239770A (en) Zinc alkaline cell
JPS63239769A (en) Zinc alkaline cell
JPS63248066A (en) Zinc alkaline battery
JPS62168344A (en) Nonaqueous electrolyte battery