JPS5931180B2 - Chikudenchi - Google Patents
ChikudenchiInfo
- Publication number
- JPS5931180B2 JPS5931180B2 JP50138323A JP13832375A JPS5931180B2 JP S5931180 B2 JPS5931180 B2 JP S5931180B2 JP 50138323 A JP50138323 A JP 50138323A JP 13832375 A JP13832375 A JP 13832375A JP S5931180 B2 JPS5931180 B2 JP S5931180B2
- Authority
- JP
- Japan
- Prior art keywords
- hydrogen
- nickel
- magnesium
- alloy
- discharge capacity
- 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.)
- Expired
Links
Classifications
-
- 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
- Battery Electrode And Active Subsutance (AREA)
Description
【発明の詳細な説明】
本発明は、酸素と陰極に貯蔵されている水素との電気化
学反応により発生したエネルギーを電気エネルギーとし
て取り出す蓄電池に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a storage battery that extracts energy generated by an electrochemical reaction between oxygen and hydrogen stored in a cathode as electrical energy.
従来から鉛/酸化鉛、ニッケル/カドミウムなどの蓄電
池が知られているが、これらの蓄電池は酸化物電極を有
するために、放電容量密度が重量および容積に関して比
較的低かつた。そこでアルカリ蓄電池の放電容量密度を
向上させるために、陰極として水素を吸蔵する電極を用
いることが提案されているが、放電容量密度が未だ十分
とは云えなかつた。本発明は、安価でしかも水素吸蔵能
が大きな材料としてマグネシウムに着目し、これにニッ
ケルを添加して放電容量密度の向上をはかつたものでわ
る。Although lead/lead oxide, nickel/cadmium, and other storage batteries are conventionally known, these storage batteries have relatively low discharge capacity densities in terms of weight and volume because they have oxide electrodes. In order to improve the discharge capacity density of alkaline storage batteries, it has been proposed to use an electrode that stores hydrogen as a cathode, but the discharge capacity density has not yet been sufficient. The present invention focuses on magnesium as an inexpensive material with a large hydrogen storage capacity, and adds nickel to it to improve the discharge capacity density.
マグネシウムぱ、’単位グラム当りの水素貯蔵量が大き
いが、電気化学的に水素を吸蔵しないために、金属水素
化合物陰極として使用しても殆んど水素の酸化反応は認
められなく、放電容量密度は零に等しいが、マグネシウ
ムにニッケルを添加することにより、電気化学的に水素
を容易に吸蔵・放出することができ、かつ放電時、アル
カリ性電解液中で水素の電気化学的酸化を促進させて水
にする機能が生ずる。Magnesium has a large hydrogen storage capacity per gram, but because it does not electrochemically absorb hydrogen, almost no hydrogen oxidation reaction is observed even when used as a metal hydride cathode, and the discharge capacity density is low. is equal to zero, but by adding nickel to magnesium, hydrogen can be easily absorbed and released electrochemically, and the electrochemical oxidation of hydrogen can be promoted in the alkaline electrolyte during discharge. The function of making water occurs.
一般に知られているマグネシウム単体およびマグネシウ
ム合金は、ガス状の水素を吸蔵して次のような金属水素
化合物を形成する。Generally known simple magnesium and magnesium alloys absorb gaseous hydrogen to form the following metal hydride compounds.
Mg+H2=MgH|・・・・・・・・・・・・・・・
(1)Mg2Ni+ 2H|=Mg|NiH4・・・・
・・・・・(2)(1)式では単位重量当りの水素吸蔵
量は約1000cc/V、(2式ではそれが45Occ
/yであり、一方MgNi2合金は、吸蔵水素量が非常
に少くない。Mg+H2=MgH|・・・・・・・・・・・・・・・
(1) Mg2Ni+ 2H|=Mg|NiH4...
...(2) In formula (1), the hydrogen storage capacity per unit weight is approximately 1000cc/V (in formula 2, it is 45Occ).
/y, and on the other hand, the MgNi2 alloy has a very small amount of absorbed hydrogen.
マグネシウム単体ではガス状の水素を多量に吸蔵するが
アルカリ電解液中ではマグネシウム表面に不働態化被膜
を形成して電気化学的に不活性となるがマグネシウム−
ニッケル合金の場合は、その不働態化皮膜の形成が出来
難くなつて電気化学的に水素の吸蔵・放出を容易になし
ていることによる。以下本発明の一実施例について詳述
する。Magnesium alone absorbs a large amount of gaseous hydrogen, but in an alkaline electrolyte, it forms a passivation film on the magnesium surface and becomes electrochemically inert.
In the case of nickel alloys, it is difficult to form a passivation film, which makes it easy to absorb and release hydrogen electrochemically. An embodiment of the present invention will be described in detail below.
・ 市販の高純度のマグネシウムおよびニッケルを高周
波溶解炉に入れ、アルゴンからなる不活性気流中で溶解
させ、ついでこれをアルゴン気流中のドライボックス中
で粉砕し、耐圧反応容器に入れたわち容器内のガスを吸
引除去し、しかるのち水素ボンベにより高純度ガスを反
応容器内に送入し5〜30kg/Cdの一定圧力に保持
し、300〜350℃まで昇温してマグネシウム−ニッ
ケル合金の水素活性化を行なつた。- Commercially available high-purity magnesium and nickel were placed in a high-frequency melting furnace and melted in an inert gas stream consisting of argon, and then ground in a dry box in an argon stream and placed in a pressure-resistant reaction vessel. The gas inside is removed by suction, and then high-purity gas is introduced into the reaction vessel using a hydrogen cylinder, maintained at a constant pressure of 5 to 30 kg/Cd, and heated to 300 to 350°C to form a magnesium-nickel alloy. Hydrogen activation was performed.
この水素化した粉末状合金から水素を除去したのち数μ
〜10数μ程度の粉末粒子にふるい分けし、ついで硫酸
ソーダ、リン酸ソーダ、ポリビニルアルコールのような
熱分解性物質を数%加えて圧縮成型し、真空中において
600〜700℃で数時間焼結して多孔性合金体とする
。After removing hydrogen from this hydrogenated powder alloy,
It is sieved into powder particles of ~10-odd microns, then compression molded with a few percent of thermally decomposable substances such as sodium sulfate, sodium phosphate, and polyvinyl alcohol, and sintered in a vacuum at 600 to 700°C for several hours. to make a porous alloy body.
得られた合金体を電極となしてアルカリ電解液中に浸漬
し、ニツケル対極を用いて充電放電を行なつた処図に示
すような結果がえられた。マグネシウムにニツケルを添
加すると放電容量密度が増加し、ニツケルの含有量が約
55重量%(合金組成Mg2Ni)附近で最大の500
AVkgを示すことがわかる。The obtained alloy body was used as an electrode and immersed in an alkaline electrolyte, and charging and discharging was performed using a nickel counter electrode.The results shown in the figure were obtained. When nickel is added to magnesium, the discharge capacity density increases, reaching a maximum of 500% when the nickel content is around 55% by weight (alloy composition Mg2Ni).
It can be seen that it shows AVkg.
ニツケルの含有量が多くなるとMgNi,組成の合金ま
ではMg,Nil:.MgNi2の共存混合物であり、
水素吸蔵能は殆んどMg2Niに律則され、MgNi,
は殆んど水素を吸蔵しないので、Mg2Niを境界とし
て放電容量密度は徐々に低下することがわかる。As the nickel content increases, it becomes MgNi, and up to alloys with the composition Mg, Nil:. A coexisting mixture of MgNi2,
Hydrogen storage capacity is mostly determined by Mg2Ni, and MgNi,
It can be seen that the discharge capacity density gradually decreases with Mg2Ni as the boundary because it absorbs almost no hydrogen.
アルカリ蓄電池用陰極としての放電容量密度は実用上か
ら少なくとも0.15Ah/t以上でないと従来のもの
と比較して特徴がないので、ニツケルの含有量は20〜
70重量%が有効である。For practical purposes, the discharge capacity density of a cathode for an alkaline storage battery must be at least 0.15 Ah/t or higher, otherwise it will have no characteristics compared to conventional ones, so the nickel content should be 20~
70% by weight is effective.
また一般の蓄電池の放電容量密度は100〜150Ah
A!程度であるので本実施例のものは実用上高い可逆容
量を示し効果的であることがわかる。なお合金体を作る
のに、マグネシウムーニツケル合金を水素化して粉末に
することなく機械的に粉砕して数μ〜数10μ程度にふ
るいわけしても良い。しかしこの場合は、合金粉末を結
着剤とともに混合し、圧縮成型したのち真空焼結し、つ
いで冷却する時に水素雰囲気中で水素を吸蔵させて多孔
性合金体とする。In addition, the discharge capacity density of general storage batteries is 100 to 150 Ah.
A! It can be seen that the present example exhibits a high reversible capacity and is effective in practice. Incidentally, in order to produce the alloy body, the magnesium-nickel alloy may be mechanically pulverized and sieved into a size of several microns to several tens of microns, without hydrogenating the magnesium-nickel alloy and turning it into powder. However, in this case, the alloy powder is mixed with a binder, compression molded, vacuum sintered, and then, when cooled, hydrogen is absorbed in a hydrogen atmosphere to form a porous alloy body.
もし強度が弱いときは、再度粉砕しで結着剤を添加し、
成型焼結して多孔体とすることもできる。以上のように
本発明は、チタンーニツケル合金等に比べると極めて廉
価である。If the strength is weak, grind it again and add a binder.
It can also be molded and sintered to form a porous body. As described above, the present invention is extremely inexpensive compared to titanium-nickel alloys and the like.
ニツケルを含むマグネシウム合金を陰極として用い、水
素を電気化学的に吸蔵させることにより放電容量密度の
良好な蓄電池を提供するものである。A storage battery with good discharge capacity density is provided by using a magnesium alloy containing nickel as a cathode and electrochemically absorbing hydrogen.
図面はマグネシウムーニツケル合金組成とエネルギー貯
蔵容量との関係線図である。The drawing is a relationship diagram between magnesium nickel alloy composition and energy storage capacity.
Claims (1)
、前記陰極に水素を電気化学的に吸蔵させたことを特徴
とする蓄電池。1. A storage battery characterized in that a magnesium alloy containing nickel is used as a cathode, and hydrogen is electrochemically occluded in the cathode.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50138323A JPS5931180B2 (en) | 1975-11-17 | 1975-11-17 | Chikudenchi |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP50138323A JPS5931180B2 (en) | 1975-11-17 | 1975-11-17 | Chikudenchi |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5261734A JPS5261734A (en) | 1977-05-21 |
| JPS5931180B2 true JPS5931180B2 (en) | 1984-07-31 |
Family
ID=15219207
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP50138323A Expired JPS5931180B2 (en) | 1975-11-17 | 1975-11-17 | Chikudenchi |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5931180B2 (en) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH578259A5 (en) * | 1972-04-06 | 1976-07-30 | Battelle Memorial Institute | |
| JPS5347487B2 (en) * | 1972-05-04 | 1978-12-21 |
-
1975
- 1975-11-17 JP JP50138323A patent/JPS5931180B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5261734A (en) | 1977-05-21 |
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