JPS58197684A - Air-zinc cell - Google Patents
Air-zinc cellInfo
- Publication number
- JPS58197684A JPS58197684A JP57077570A JP7757082A JPS58197684A JP S58197684 A JPS58197684 A JP S58197684A JP 57077570 A JP57077570 A JP 57077570A JP 7757082 A JP7757082 A JP 7757082A JP S58197684 A JPS58197684 A JP S58197684A
- Authority
- JP
- Japan
- Prior art keywords
- air
- zinc
- pole
- zinc cell
- mixed
- 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
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
-
- 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
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Hybrid Cells (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、空気電池の空気極の改良に関して、電池性能
の向上並びに電池作成の簡素化を目的としたものである
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improving the air electrode of an air battery, and aims at improving battery performance and simplifying battery production.
従来の空気電池は、粉状活性炭または粒状活性炭な、タ
ール、ピッチ等と混ぜ、成型焼成しさらに撥水性な持た
せる為にテフロン樹鍾等で撥水処理し、それをニッケル
ネット等に薄膜状に加圧、成型したものt空気極として
°用いていた。Conventional air batteries are made by mixing powdered activated carbon or granular activated carbon with tar, pitch, etc., molding and firing it, and then treating it with Teflon to make it water repellent. It was pressurized and molded and used as an air electrode.
ところが上記従来品では、盤状の51E型及び強度を持
たぜる為に、本来ポーラスである活性炭にわざわざター
ル、ピッチ等を添加し、その為4−ラスな粒子間がふさ
がりそれを防ぐ為に、高温で焼成する必要があったばか
りでなく、その上撥水性を持たせる為(、フラノ樹@を
添加又は含浸させ、さら(焼成するという手間な要して
いた1
またg!気電池は、21!!気、電解質、成極の接する
界面すなわち三相界面の構成いかんが電池性能の醍占を
決定するが、三田界面の形成がうまくいかないと電池性
能【光分に発揮できない。However, in the above conventional product, tar, pitch, etc. are intentionally added to the activated carbon, which is originally porous, in order to give it plate-shaped 51E type and strength, and as a result, the spaces between the 4-rus particles are blocked. Not only did it have to be fired at a high temperature, but it also required the hassle of adding or impregnating flannel wood to make it water repellent and then firing it. 21!! The composition of the three-phase interface, that is, the interface where air, electrolyte, and polarization meet, determines the performance of the battery, but if the formation of the Mita interface is not successful, the battery performance cannot be achieved.
従来これY改良する為の手段としては、撥水材の配合比
率を変化したり、銀(またはその酸化物)、/#ラノク
ム、白金等の貴会−を触媒として空気極に添加するとい
う手段がとられていたが、電池性能′lk:維持、向丘
させるには触媒等の添加量を多くする必要があり、また
、IfIgIitものとなっていた。Conventional methods for improving this include changing the blending ratio of water repellent materials, or adding silver (or its oxide), silver (or its oxide), /#ranocum, platinum, etc. to the air electrode as a catalyst. However, in order to maintain and improve the battery performance, it was necessary to increase the amount of catalyst, etc. added, and ifIgIit was required.
本発明はこの点を根本的に改良したもので、酸化第二銅
を触媒とする触媒層Y形成し、かつ空気極としては、焼
成することなく、アセチレンブランクと微粉状四フッ化
エチレン樹脂を単に混合するだけで電池性能な発揮する
という、触媒層及び空気極より構成される触匈の活性化
空気層とでもいうべきものな構成する点が従来にはみら
れない飛躍的な技術改良となっている。The present invention fundamentally improves this point, and forms a catalyst layer Y using cupric oxide as a catalyst, and as an air electrode, an acetylene blank and finely powdered tetrafluoroethylene resin are used without firing. It is a dramatic technological improvement that has not been seen before in that it consists of what can be called an activated air layer of the catalyst layer and the air electrode, which allows the battery to perform well just by mixing it. It has become.
その特徴は、放1時の負荷による電圧降下も少なく、ま
た製1隻も簡素で安1曲な醜媒ゲ1史用する空気〜亜鉛
直池?実現し得たところにある。Its characteristics are that there is little voltage drop due to the load when it is released, and it is simple and cheap to manufacture. This is something that could have been achieved.
本発明σ)空気〜亜鉛電池C1触媒−が酸化第2銅、黒
鉛及び微粉状4フッずヒエチレン樹幡ン混合したものか
らなり、空気iがアセチレンブラック及び微粉状47ツ
化エチレン衝脂馨混合したものからなり、触媒層がセ・
ぐレータ−と空気極との関に層状に構成さnていること
¥特徴とする空気〜亜鉛電池である、
本発明について図面に基づいて説明する。In the present invention σ) Air - zinc battery C1 catalyst - is made of a mixture of cupric oxide, graphite and finely powdered 4-fluoride ethylene resin, and air i is a mixture of acetylene black and finely powdered 47-ethylene chloride resin. The catalyst layer is made of
The present invention, which is an air-zinc battery characterized by being structured in layers between a regulator and an air electrode, will be explained based on the drawings.
illは陰極板、(2)は常法により水銀氷化した亜鉛
粒とか性カリ液にオA/?キシメチルセルローx(CM
C)Yl 〜1018かしたものからなるrル状炬鉛負
極、(3)はそのグル状電解液を保持する為にもうけら
れた不繊布製電解液保持層、(4)は不縁布製七ノぐレ
ータ−1(7)は空気透過性の導電材よりなる撥水処理
した集電体、(8)は空気穴な示している。(1Gは活
性化空気層であり、触媒層(51と電気極(6)とから
なる。陽極の空気極(6)は、アセチレンブラックY:
微粉状47ツ化エチレン樹脂と混合し、さらに加圧、成
型したものである。(5)は触媒層で酸化第二鋼を触媒
として黒鉛Y4[材とし、微粉状四フッ化エチレン樹脂
ヲ撥水剤とする混合物からなる層である。(9)は従来
の焼成した炭素極(空気極)ン示したものである。ill is the cathode plate, and (2) is mercury-frozen zinc grains or potash solution using the usual method. xymethylcellulose x (CM
C) An r-shaped lead negative electrode made of Yl ~ 1018, (3) is a nonwoven fabric electrolyte holding layer provided to hold the glue-like electrolyte, and (4) is a nonwoven fabric seven. Nogulator 1 (7) is a water-repellent current collector made of an air-permeable conductive material, and (8) is an air hole. (1G is an activated air layer, consisting of a catalyst layer (51) and an electric electrode (6). The air electrode (6) of the anode is acetylene black Y:
It is mixed with finely powdered 47-ethylene resin and further pressurized and molded. (5) is a catalyst layer consisting of a mixture of oxidized steel as a catalyst, graphite Y4 as a material, and finely powdered tetrafluoroethylene resin as a water repellent. (9) shows a conventional fired carbon electrode (air electrode).
本発明では覆普比で触媒酸化第二鋼IK対し、導電材の
黒鉛0.5〜2、撥水材として微粉状4して置く。空気
極は焼成することなくアセチレンブラック0.05〜0
.5微粉状四フッ化エチレン樹脂0.05〜0.5を混
じ、加圧封入することにより製造されろ。こうすること
により、セパレーターを介して(6)の空気極と(2)
の亜鉛負極との関に空気〜頃鉛亀池V*成すると共に、
(5)の触媒層の酸化第2銅にょる減極能も同時に@憚
され、より高い電圧を#持、発揮するものである。In the present invention, graphite as a conductive material is 0.5 to 2, and fine powder is 4 as a water repellent to catalytically oxidized second steel IK. The air electrode is coated with acetylene black 0.05 to 0 without baking.
.. 5. It is manufactured by mixing 0.05 to 0.5 of a finely powdered polytetrafluoroethylene resin and sealing the mixture under pressure. By doing this, the air electrode in (6) and the air electrode in (2) can be connected through the separator.
At the same time that air is formed between the zinc negative electrode and the zinc negative electrode,
The depolarization ability of the catalyst layer (5) due to cupric oxide is also suppressed at the same time, allowing it to maintain and exhibit a higher voltage.
(実施例)
グル状の亜鉛負極として、5嗟永化唾鉛粒0、5 fl
に対し、30%KOH液(ZnO飽和、3憾CMC含有
によりグル化) 1.0 mlを混じたものを用いた。(Example) As a glue-like zinc negative electrode, 5 fl.
In contrast, a mixture of 1.0 ml of 30% KOH solution (saturated with ZnO and glued by containing 3 CMC) was used.
また、11!!極たる空気極としては、市販のアセチレ
ンブラック0.1 、lil K対し、微粉状4フッ化
エチレン樹脂0.1gと混じ加圧封入したものを用いた
。触媒層としては酸化第2鋼0.2 gに対し、黒鉛0
.11微粉状4フツ化エチレン樹脂0.19を添加、混
合したもの音用いた。上記のようKして作成した空気〜
亜鉛電池な4oΩで放電した結果が第2図である。ここ
で囚は本発明法による活性化空気層な有する空気〜亜鉛
電池、(B)は従来の焼成式炭素極(銀粉触媒含有)の
′g!気rf4 k有する空気〜亜鉛電池の40Ω負荷
の放電曲線である。Also, 11! ! As the ultimate air electrode, commercially available acetylene black 0.1 and lil K were mixed with 0.1 g of finely powdered tetrafluoroethylene resin and sealed under pressure. As a catalyst layer, 0.2 g of oxidized second steel and 0 graphite were used.
.. 11 A mixture of 0.19% of finely powdered tetrafluoroethylene resin was added and mixed. Air created by K as above~
Figure 2 shows the results of discharging a zinc battery at 40Ω. Here, the cell is an air-zinc battery having an activated air layer according to the method of the present invention, and (B) is a conventional calcined carbon electrode (containing a silver powder catalyst). Figure 3 is a 40Ω load discharge curve of an air-to-zinc battery with RF4K.
図に示される砿に本発明になる空気〜亜鉛電池は、安価
な原料及び簡便な構成で、なおかつより優れた電池性能
が発揮されていることは明確でその工業的価値は大なる
ものである。As shown in the figure, it is clear that the air-zinc battery of the present invention uses inexpensive raw materials and a simple structure, and also exhibits superior battery performance, and its industrial value is great. .
第1図は本発明による空気〜亜鉛電池の断面図である。
第2図は従来の空気〜亜鉛電池の断面図である。
1、・・・陰極板 2.・・・グル状の亜鉛負極3
、・・・電解液保持層4.・・・セ14’ L/−ター
5、・・・触媒層 6.・・・空気極7、・・・集
電体 8.・・・空気穴9、・・・従来の焼成式炭
素極(Ag触媒)10、・・・活性化空気層
第3図は本発明の電池の40Ω負荷の放電曲線な従来の
ものと対比して示す図である。
第1図
第2図FIG. 1 is a cross-sectional view of an air-zinc battery according to the present invention. FIG. 2 is a cross-sectional view of a conventional air-zinc battery. 1. Cathode plate 2. ... Glue-shaped zinc negative electrode 3
, . . . Electrolyte holding layer 4. ...Catalyst layer 6. ... air electrode 7, ... current collector 8. ...air hole 9, ...conventional calcined carbon electrode (Ag catalyst) 10, ...activated air layer Fig. 3 shows the discharge curve of the battery of the present invention under a 40Ω load in comparison with the conventional one. FIG. Figure 1 Figure 2
Claims (1)
レン樹riv混合したものからなり、空気極がアセチレ
ンブラック及び微粉状4フツ化エチレン樹11ii ’
に混合したものからなり、触媒層が竜−々レーターE空
気極との関に層状に構成されていることを*iとする空
気〜東鉛電池。The catalyst layer is oxidized No. 241. .. The air electrode is made of a mixture of acetylene black and finely powdered tetrafluoroethylene tree riv, and the air electrode is made of acetylene black and finely powdered tetrafluoroethylene tree
*i is an air-to-east lead battery consisting of a mixture of the above and the catalyst layer is structured in a layered manner in relation to the Dragon Lator E air electrode.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57077570A JPS58197684A (en) | 1982-05-11 | 1982-05-11 | Air-zinc cell |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57077570A JPS58197684A (en) | 1982-05-11 | 1982-05-11 | Air-zinc cell |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58197684A true JPS58197684A (en) | 1983-11-17 |
Family
ID=13637667
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57077570A Pending JPS58197684A (en) | 1982-05-11 | 1982-05-11 | Air-zinc cell |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58197684A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002001666A2 (en) * | 2000-06-28 | 2002-01-03 | The Gillette Company | Hydrogen recombination catalyst |
WO2002001655A2 (en) * | 2000-06-28 | 2002-01-03 | The Gillette Company | Hydrogen recombination catalyst |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4855333A (en) * | 1971-11-16 | 1973-08-03 |
-
1982
- 1982-05-11 JP JP57077570A patent/JPS58197684A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4855333A (en) * | 1971-11-16 | 1973-08-03 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002001666A2 (en) * | 2000-06-28 | 2002-01-03 | The Gillette Company | Hydrogen recombination catalyst |
WO2002001655A2 (en) * | 2000-06-28 | 2002-01-03 | The Gillette Company | Hydrogen recombination catalyst |
WO2002001655A3 (en) * | 2000-06-28 | 2002-06-27 | Gillette Co | Hydrogen recombination catalyst |
WO2002001666A3 (en) * | 2000-06-28 | 2002-06-27 | Gillette Co | Hydrogen recombination catalyst |
US6500576B1 (en) | 2000-06-28 | 2002-12-31 | The Gillette Company | Hydrogen recombination catalyst |
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