JPS58165249A - Anode plate for alkaline battery - Google Patents
Anode plate for alkaline batteryInfo
- Publication number
- JPS58165249A JPS58165249A JP57048402A JP4840282A JPS58165249A JP S58165249 A JPS58165249 A JP S58165249A JP 57048402 A JP57048402 A JP 57048402A JP 4840282 A JP4840282 A JP 4840282A JP S58165249 A JPS58165249 A JP S58165249A
- Authority
- JP
- Japan
- Prior art keywords
- cadmium
- anode
- nickel
- hydroxide
- metal
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0438—Processes of manufacture in general by electrochemical processing
- H01M4/044—Activating, forming or electrochemical attack of the supporting material
- H01M4/0445—Forming after manufacture of the electrode, e.g. first charge, cycling
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/24—Electrodes for alkaline accumulators
- H01M4/246—Cadmium electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/624—Electric conductive fillers
- H01M4/626—Metals
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
- H01M2004/027—Negative electrodes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0402—Methods of deposition of the material
- H01M4/0404—Methods of deposition of the material by coating on electrode collectors
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/66—Selection of materials
- H01M4/661—Metal or alloys, e.g. alloy coatings
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/64—Carriers or collectors
- H01M4/70—Carriers or collectors characterised by shape or form
- H01M4/72—Grids
- H01M4/74—Meshes or woven material; Expanded metal
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Battery Electrode And Active Subsutance (AREA)
Abstract
Description
【発明の詳細な説明】
活物質としてニッケル酸化物を1崗に、カドミウムを負
極に使用したアルカリ蓄電池は、充電時に正−から発生
する酸素を負極で消費させるという機構を利用して、完
全密閉化ができるという、他の二次電池には類の無い特
長を有している。[Detailed Description of the Invention] Alkaline storage batteries that use nickel oxide as the active material and cadmium as the negative electrode utilize a mechanism in which oxygen generated from the positive electrode is consumed at the negative electrode during charging, and are completely sealed. It has a feature unparalleled by other secondary batteries:
しかしWI数の素電池を直列に接続した場合、素電池間
のW濾に大小の唾があれば、放電時に谷型が少ない電池
は、正常な終止電圧を過ぎて、いわゆる過放′鑞を生ず
る事になる。However, when WI number of unit cells are connected in series, if there are large and small gaps in the W filter between the units, the battery with few valleys during discharge will exceed the normal final voltage and cause so-called overdischarge. It will happen.
過放電を行うと、電流に比例して1臘からは水素、負極
からは酸素を生じるが、特に水素はtllIl11円で
吸収される割合が−めで小さい為、密閉電池に於ては水
素を発生させる事は絶対に避けなければならない。従っ
てその対策として密閉電池に使用する正−に、は活物質
に対重物質である水酸化カドミウムや、酸化カドミウム
等のカドミウム化合物を添加する方法がとられている。When overdischarging, hydrogen is generated from the negative electrode in proportion to the current, and oxygen is generated from the negative electrode, but since the rate of absorption of hydrogen is particularly small at tllIl11 yen, hydrogen is generated in a sealed battery. This must be avoided at all costs. Therefore, as a countermeasure to this problem, a method has been adopted in which a cadmium compound such as cadmium hydroxide or cadmium oxide, which is a heavy substance, is added to the active material used in sealed batteries.
すなわち1囁が過放電領域に達した場合に、カドミウム
化合物が金属カドミウムに還元される反応が生じ、この
間水素発生を抑制する事ができるものである。That is, when one discharge reaches the overdischarge region, a reaction occurs in which the cadmium compound is reduced to metal cadmium, and hydrogen generation can be suppressed during this period.
またカドミウム化合物を添加すると、充電時の酸素発生
電位を上昇せしめ、正極の充電効率を高めるという効果
もある。Addition of a cadmium compound also has the effect of increasing the oxygen generation potential during charging and increasing the charging efficiency of the positive electrode.
しかし通常の充放電には不要であるだけでなく、絶健物
に等しいカドミウム化合物が存在することによって、正
−円の電気抵抗を嶋め、特に放電時の電圧降下を大きく
するとともに、活物質利用率も低下させるという欠点が
あった。However, not only is it unnecessary for normal charging and discharging, but the presence of cadmium compounds, which is equivalent to a completely healthy substance, lowers the electric resistance of the positive circle, particularly increases the voltage drop during discharge, and causes active material It also had the disadvantage of lowering the utilization rate.
本発明は以上述べた従来の欠点を解消し、カドミウム化
合物を添加したアルカリ電池用1勤の特性を向上せしめ
る躯を可能ならしめるもので、正極中に含まれるカドミ
ウムの一部あるいは全部をあらかじめ金属カドミウムと
しておく事によって、正極門番ζおける電子電導性を高
めるCとが出来るという事実に基くもので、以下、実施
倒位び従来品と比較した結果について詳細な説明を行う
。The present invention solves the above-mentioned conventional drawbacks and makes it possible to create a structure that improves the characteristics of a first-layer alkaline battery containing a cadmium compound. This is based on the fact that by using cadmium, C can be used to increase the electronic conductivity in the positive electrode gatekeeper ζ.Hereinafter, a detailed explanation will be given of the results of the actual displacement and comparison with conventional products.
実−例1: 少量の水酸化コバルトを含む水酸化ニッケ
ルが40[11%、カーボニツニルケル粉末が85[1
%、酸化カドミウムが15@置%及び結□
着剤として、ポリエチレン、粉末10 [1%とから一
部
なる原料混合物を、中心に集電体となるニッケル網をは
さんだ厚さ1.5fiで50 X 5G mの寸法に加
圧成形し、理論容量1.8ムhの正極を製作した。Practical Example 1: Nickel hydroxide containing a small amount of cobalt hydroxide was 40 [11%] and carbon nickel powder was 85 [1%].
%, cadmium oxide was placed at 15% and □ As an adhesive, a raw material mixture consisting of polyethylene powder and 10% and 1% of cadmium oxide was mixed with a thickness of 1.5fi with a nickel mesh as a current collector sandwiched in the center. A positive electrode with a theoretical capacity of 1.8 μm was manufactured by pressure molding to a size of 50×5 G m.
これを比重が1.22の水酸化ナトリウム水溶液中でニ
ッケル仮を相手臘として、860mA の電池で8時
間カソード方向に通電を行い一旦、はとんどオペでのカ
ドミウム化合物を金属カドミウムに転化させた本発明に
よる1翫を四とする。This was placed in an aqueous sodium hydroxide solution with a specific gravity of 1.22, using nickel as a temporary partner, and an 860 mA battery was used to supply electricity in the cathode direction for 8 hours to convert the cadmium compound in the operation into metallic cadmium. According to the present invention, one rod is four.
実権例2: atl記実施例における酸化カドミウム
の代りに金属カドミウム粉末を加え、他の組成。Practical example 2: Metal cadmium powder was added instead of cadmium oxide in the atl example, and other compositions were used.
形状は同一にして製作した正極を−)とする。The positive electrode manufactured with the same shape is designated as -).
更に従来例として、実−例1の四の正極と同一組成、形
状に成形した・だけで、金属カドミウムへの転化をしな
い従来の正l1I(C1とを作った。Furthermore, as a conventional example, a conventional positive 11I (C1) was made which was molded to have the same composition and shape as the positive electrode in Example 1, but was not converted into metallic cadmium.
それぞれの1唾を、比t1.25の水酸化カリウム水溶
液中で同じ寸法の焼結式カドミウム負−板2枚を相手板
として、25℃の温度で、270mムの電流で16時間
充電した後1.2ムの電流で放電を行っ々
たところ、第1図に示す様な放電特性を4た。After charging each spit with a current of 270 mm at a temperature of 25°C for 16 hours using two sintered cadmium negative plates of the same size as mating plates in a potassium hydroxide aqueous solution with a ratio T of 1.25. When discharge was carried out at a current of 1.2 μm, the discharge characteristics as shown in FIG. 1 were obtained.
第1図から明らか2様に、金属カドミウムを含むモー板
体)とφ)の放電″1特性は、従来の正−仮()の放電
特性に比べて放電電位が高く、しかも放電時間の長い優
れたものであった。また過放電における特性も(前世)
何れも良好であった。その理由として考えられることは
、定かではないが本発明による正FjjA板中にあらか
じめ存在せしめられた金属カドミウムは、正極板の通常
の充電において、ソノ何割かは水酸化カドミウムに変化
するが、全てが水酸化カドミウムに変化するのではなく
、一部は安定な金属カドミウムの状態で残存して、正−
中の電導性を高めるという良好な働きをしているものと
考えられる。As is clear from Figure 1, the discharge characteristics of the Maw plates) and φ) containing metal cadmium have a higher discharge potential and a longer discharge time than the conventional positive-temporal () discharge characteristics. It was excellent. Also, the characteristics against overdischarge were also good (previous life).
All were good. The reason for this is not certain, but some of the metal cadmium pre-existing in the positive FJJA plate according to the present invention changes to cadmium hydroxide during normal charging of the positive electrode plate, but all of it changes to cadmium hydroxide. Rather than changing to cadmium hydroxide, some of it remains in the stable state of metallic cadmium and becomes positive.
It is thought that it has a good effect of increasing the conductivity inside.
実施例では、活物質、電導材等の粉末を加圧成形して製
造するいわゆる粉末加圧式正極板に嘴して述べたが水酸
化ニッケルを1:たる活物質とし、カドミウムを含むア
ルカリ電池用正[1仮であれば、多孔質のニッケル焼結
体に活物質を含浸した焼結式正極板、発泡状ニッケルシ
ートにペースト状活物質を充填したペースト式蔭板等、
構造、製法の違いにか\わらず、本発明の目的を達成で
きる事は言うまでもない。In the example, the so-called powder press type positive electrode plate, which is manufactured by pressure molding powder of active material, conductive material, etc., was described. Positive [1] If it is temporary, a sintered positive electrode plate made of a porous nickel sintered body impregnated with an active material, a paste type negative plate made of a foamed nickel sheet filled with a paste active material, etc.
It goes without saying that the object of the present invention can be achieved regardless of the difference in structure and manufacturing method.
第1図は放電特性を比較したもので、四、(B)は本発
明による正m 、 io+は従来の正極を承す門λ
1 図
抜 俄 呼 旬 (発)Figure 1 shows a comparison of discharge characteristics, where (4) (B) is the positive electrode according to the present invention, and io+ is the gate λ that accepts the conventional positive electrode.
1 Unillustrated call Shun (departure)
Claims (1)
ミウム化合物及び金属カドミウムを含有しtこ事を特徴
とするアルカリ 電池用正鑞仮。 !、金金力カドミウム、カドミウム化合物の一部をvi
、気化学的に還元を行う事によって変化させて得たもの
である特許請求の範囲第1項記載のアルカリ電池用正礪
板。 $、金属カドミウムは、活物質としての水酸化ニッケル
とともにカドミウム粉末の形で添加することを特徴とす
るアルカリ電池中正−板。[Claims]! A positive solder for alkaline batteries characterized by containing nickel hydroxide as an active material, and a cadmium compound and metal cadmium as additives. ! , Kinkinriki cadmium, some of the cadmium compounds vi
2. The regular plate for alkaline batteries according to claim 1, which is obtained by changing the plate by vapor chemical reduction. $, An alkaline battery center plate characterized in that metal cadmium is added in the form of cadmium powder together with nickel hydroxide as an active material.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57048402A JPS58165249A (en) | 1982-03-25 | 1982-03-25 | Anode plate for alkaline battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57048402A JPS58165249A (en) | 1982-03-25 | 1982-03-25 | Anode plate for alkaline battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58165249A true JPS58165249A (en) | 1983-09-30 |
Family
ID=12802307
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57048402A Pending JPS58165249A (en) | 1982-03-25 | 1982-03-25 | Anode plate for alkaline battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58165249A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60258857A (en) * | 1984-06-06 | 1985-12-20 | Matsushita Electric Ind Co Ltd | Sealed type nickel-cadmium storage battery |
-
1982
- 1982-03-25 JP JP57048402A patent/JPS58165249A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS60258857A (en) * | 1984-06-06 | 1985-12-20 | Matsushita Electric Ind Co Ltd | Sealed type nickel-cadmium storage battery |
JPH0679484B2 (en) * | 1984-06-06 | 1994-10-05 | 松下電器産業株式会社 | Sealed nickel-cadmium storage battery |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3060254A (en) | Bonded electrodes | |
JP3923157B2 (en) | Alkaline storage battery | |
US3883368A (en) | Alkaline aluminum-air/zinc-manganese dioxide hybrid battery | |
US4130696A (en) | Conductive diluent for pressed nickel electrodes | |
US4427751A (en) | Alkaline battery | |
JPS58165249A (en) | Anode plate for alkaline battery | |
JPH0582023B2 (en) | ||
KR100943751B1 (en) | Nickel-metal hydride secondary battery | |
JPS61208755A (en) | Pasted negative cadmium plate for sealed alkaline storage battery | |
JPH06260166A (en) | Nickel electrode for alkaline storage battery | |
JPS58163172A (en) | Alkaline zinc storage battery | |
JPS5931177B2 (en) | Zinc electrode for alkaline storage battery | |
JPH06101331B2 (en) | Alkaline zinc storage battery | |
JPS60198066A (en) | Alkaline storage battery | |
JP4411860B2 (en) | Storage battery | |
JPH0414758A (en) | Lead-acid accumulator | |
JP3287386B2 (en) | Nickel electrode for alkaline storage battery | |
JPH02262244A (en) | Sealed alkaline battery | |
JP2022114305A (en) | Negative electrode for fluoride ion secondary battery and fluoride ion secondary battery having the same | |
JPH0560220B2 (en) | ||
JPH10208746A (en) | Sealed lead-acid battery | |
JPH0576743B2 (en) | ||
JPH0513078A (en) | Nickel positive electrode for alkaline battery | |
JPH0544142B2 (en) | ||
JPH0687417B2 (en) | Alkaline zinc storage battery |