JP5385570B2 - Batteries using acidic electrolyte - Google Patents

Batteries using acidic electrolyte Download PDF

Info

Publication number
JP5385570B2
JP5385570B2 JP2008228407A JP2008228407A JP5385570B2 JP 5385570 B2 JP5385570 B2 JP 5385570B2 JP 2008228407 A JP2008228407 A JP 2008228407A JP 2008228407 A JP2008228407 A JP 2008228407A JP 5385570 B2 JP5385570 B2 JP 5385570B2
Authority
JP
Japan
Prior art keywords
metal
battery
acidic electrolyte
conductive member
separator
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.)
Active
Application number
JP2008228407A
Other languages
Japanese (ja)
Other versions
JP2010062074A (en
Inventor
久美子 吉井
秀男 上野
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.)
ENVIRONMENTAL SCIENCE INSTITUTE, LTD.
Original Assignee
ENVIRONMENTAL SCIENCE INSTITUTE, 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 ENVIRONMENTAL SCIENCE INSTITUTE, LTD. filed Critical ENVIRONMENTAL SCIENCE INSTITUTE, LTD.
Priority to JP2008228407A priority Critical patent/JP5385570B2/en
Publication of JP2010062074A publication Critical patent/JP2010062074A/en
Application granted granted Critical
Publication of JP5385570B2 publication Critical patent/JP5385570B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • 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

  • Sealing Battery Cases Or Jackets (AREA)
  • Hybrid Cells (AREA)

Description

本発明は、酸性電解質を用いた一次電池及び二次電池に関するものである。   The present invention relates to a primary battery and a secondary battery using an acidic electrolyte.

従来、電池としては多種多様のものがあり、例えば使い捨ての一次電池や、充電可能な二次電池や燃料電池等が代表的な化学電池であり、そのほか光電池や太陽電池等の物理電池が知られている。   Conventionally, there are a wide variety of batteries, for example, disposable primary batteries, rechargeable secondary batteries, fuel cells, and the like are typical chemical batteries, and other physical batteries such as photovoltaic cells and solar cells are known. ing.

周知のように、一次電池は充電できず、二次電池は充電できるが充電時には電源に接続して通電しなければならないといった欠点がある。又、燃料電池は、電極触媒として白金を使用するため高価となる。更に、補聴器等に使用される空気電池は、一旦シールを剥がして空気を供給すると、その後シールを貼り直しても内部での化学反応を完全に停止することができず、自然放電をとめることができない欠点がある。   As is well known, the primary battery cannot be charged and the secondary battery can be charged. However, there is a drawback that the battery must be connected to a power source and charged when charged. In addition, the fuel cell is expensive because platinum is used as an electrode catalyst. Furthermore, once the air battery used in a hearing aid or the like is peeled off and air is supplied, the internal chemical reaction cannot be stopped completely even after the seal is reapplied, and spontaneous discharge can be stopped. There is a disadvantage that cannot be done.

一方、リザーブ電池として知られているマグネシウム電池は、比較的大きな起電力を得られるが、放電持続時間が短いことや塩化銀などの高価な材料を用いる等のことから広く普及することは難しいとされている。このマグネシウム電池は、まだまだ未開発の分野であり、それに対する情報量も非常に少ない。例えば特許文献1、2等の中に僅かに記載されている程度である。   On the other hand, a magnesium battery known as a reserve battery can obtain a relatively large electromotive force, but it is difficult to spread widely due to short discharge duration and the use of expensive materials such as silver chloride. Has been. This magnesium battery is still an undeveloped field, and there is very little information on it. For example, it is only described in Patent Documents 1 and 2 or the like.

特表2008−523211号公報Special table 2008-523211 gazette 特表平9−501007号公報JP-T 9-501007

本件発明者らは、マグネシウム電池に関連する研究を重ねた結果、酸性電解質を用いることで従来よりも起電力がはるかに大きく、しかも電源に接続せずに負極の金属を取り替えるだけで充電できることを知見して本発明を完成するに至った。即ち、本発明は、酸性電解質を用いた電池(一次電池及び二次電池)を提供することを目的とする。   As a result of repeated research related to the magnesium battery, the present inventors have found that the use of an acidic electrolyte has a much higher electromotive force than before and can be charged simply by replacing the metal of the negative electrode without connecting to a power source. The inventors have found out that the present invention has been completed. That is, an object of the present invention is to provide a battery (primary battery and secondary battery) using an acidic electrolyte.

上記の目的を達成するための手段として、本発明の請求項1は、少なくとも負極となる金属と、正極となる導電部材とを、前記金属と導電部材との間にセパレータを配置し、前記金属とセパレータとの間に吸水・保湿部材を配置して、重ね合わせて重合体を形成し、前記導電部材における前記金属に対向する側には酸性電解質が付着され、前記金属に対向しない側には陽極触媒を配置して成る酸性電解質を用いた電池であって、
前記吸水・保湿部材に前記金属を取り付け、当該吸水・保湿部材と共に前記金属を交換することを特徴とする。
As means for achieving the above object, claim 1 of the present invention comprises at least a metal serving as a negative electrode and a conductive member serving as a positive electrode, and a separator disposed between the metal and the conductive member. A water absorbing / moisturizing member is disposed between the separator and the separator to form a polymer, and an acidic electrolyte is attached to a side of the conductive member facing the metal, and a side not facing the metal. A battery using an acidic electrolyte formed by arranging an anode catalyst ,
The metal is attached to the water absorption / humidity retention member, and the metal is exchanged together with the water absorption / humidity retention member .

少なくとも負極となる金属と、正極となる導電部材とを重ね合わせて重合体を形成し、前記導電部材における前記金属に対向する側には酸性電解質が付着され、前記重合体を前記金属が外側となるようにして折り曲げ、前記導電部材の内側に生じた空間部に陽極触媒を配置して成る酸性電解質を用いた電池とすることができる。 A metal serving as least a negative electrode, by superposing a conductive member serving as a positive electrode to form a polymer, wherein the side facing to the metal in the conductive member is attached acidic electrolyte, the metal the polymer bent so as to be outside, it is possible to batteries using an acidic electrolyte comprising placing an anode catalyst in the space produced inside the conductive member.

少なくとも負極となる金属と、正極となる導電部材とを重ね合わせて重合体を形成し、前記導電部材における前記金属に対向する側には酸性電解質が付着され、前記重合体を前記金属が内側となるようにして折り曲げ、前記導電部材の外側に陽極触媒を配置して成る酸性電解質を用いた電池とすることができる。 A metal serving as least a negative electrode, by superposing a conductive member serving as a positive electrode to form a polymer, wherein the side facing to the metal in the conductive member is attached acidic electrolyte, the metal the polymer A battery using an acidic electrolyte which is bent so as to be inside and an anode catalyst is arranged outside the conductive member can be obtained.

前記重合体を筒状に屈曲形成とすることができる。 It can be bent to the polymeric into a cylindrical shape.

(削除) (Delete)

(削除) (Delete)

(削除) (Delete)

本発明の請求項2は、請求項1記載の酸性電解質を用いた電池において、前記重合体を電気絶縁性の保護部材で保護したことを特徴とする。 According to a second aspect of the present invention, in the battery using the acidic electrolyte according to the first aspect , the polymer is protected by an electrically insulating protective member.

本発明の請求項3は、請求項1又は請求項2記載の酸性電解質を用いた電池において、前記重合体を電気絶縁性の容器内に収納し、この容器に空気導入孔を設けたことを特徴とする。 According to a third aspect of the present invention, in the battery using the acidic electrolyte according to the first or second aspect , the polymer is housed in an electrically insulating container, and an air introduction hole is provided in the container. Features.

上記請求項1の発明によれば、負極と正極とをリード線で接続すると負極から金属陽イオンが溶出されると共に、電子がリード線を介して負極から正極側へ移動し、正極の表面に供給された酸素は、電子を取り込んで水を生成する。これにより、正極から負極側に電流がながれて電気を取り出すことができる。この場合、負極から発生する金属陽イオンと酸性電解質中の錯イオンとが結合して錯体が形成されるが、この錯体は電池化学反応によって生じる生成水によって簡単に溶解するため負極の金属表面に付着せず、大きな起電力が得られると共に起電力の低下を抑えることができる。又、正極には空気を供給して反応させるが、負極側を酸性電解質と接触させないことにより化学反応を完全に停止させることができる。
前記金属と導電部材との間にセパレータを配置したので負極と正極との領域を区画することができ、電池化学反応を確実に行うことができる。
前記金属と導電部材との間、又は前記金属とセパレータとの間に吸水・保湿部材を配置したので、金属に対して酸性電解質を確実に且つ平均して接触させることができ、常時安定した起電力を得ることができる。又、電池化学反応によって負極の金属が溶けて無くなった(以下、溶滅という)時に、当該金属を取り替えることにより継続して使用することができる。これにより、外部電源に接続せずに負極の金属を取り替えるだけで充電が可能な二次電池を形成することができる
前記吸水・保湿部材に金属を取り付け、当該吸水・保湿部材と共に金属を交換するので、金属の取り替えが簡単にできると共に金属の残渣を残すことなく綺麗に取り除くことができる。
According to the first aspect of the present invention, when the negative electrode and the positive electrode are connected by the lead wire, the metal cation is eluted from the negative electrode, and the electrons move from the negative electrode to the positive electrode side via the lead wire, so that The supplied oxygen takes in electrons and generates water. Thereby, a current flows from the positive electrode to the negative electrode side, and electricity can be taken out. In this case, the metal cation generated from the negative electrode and the complex ion in the acidic electrolyte are combined to form a complex, but this complex is easily dissolved by the water generated by the battery chemical reaction, and thus the complex is formed on the metal surface of the negative electrode. A large electromotive force can be obtained without adhesion, and a decrease in electromotive force can be suppressed. In addition, although air is supplied to the positive electrode to react, the chemical reaction can be completely stopped by not contacting the negative electrode side with the acidic electrolyte.
Since the separator is disposed between the metal and the conductive member, the region between the negative electrode and the positive electrode can be partitioned, and the battery chemical reaction can be performed reliably.
Since a water absorbing / moisturizing member is disposed between the metal and the conductive member or between the metal and the separator, the acid electrolyte can be reliably and averaged in contact with the metal, and stable and stable Electric power can be obtained. Further, when the metal of the negative electrode is melted and lost by the battery chemical reaction (hereinafter referred to as erosion), it can be used continuously by replacing the metal. Thereby, the secondary battery which can be charged only by replacing | exchanging the metal of a negative electrode, without connecting with an external power supply can be formed .
Since a metal is attached to the water absorbing / moisturizing member and the metal is exchanged together with the water absorbing / moisturizing member, the metal can be easily replaced and can be neatly removed without leaving a metal residue.

少なくとも負極となる金属と、正極となる導電部材(金属に対向する側に酸性電解質を塗布する)とを重ね合わせた重合体を、前記金属が外側となるようにして二つに折り曲げてその内側空間に陽極触媒を配置することで小型・軽量の一次電池を形成することができる。 A metal serving as the negative electrode at least, the superposed polymer and a conductive member serving as a positive electrode (applying the acid electrolyte on the side opposite to the metal), the metal is bent in two so as to be outside its By arranging the anode catalyst in the inner space, a small and light primary battery can be formed.

前記のものとは反対方向に、即ち前記金属が内側となるようにして二つに折り曲げて前記導電部材の外側に陽極触媒を配置することで小型・軽量の一次電池を形成することができる。 A small and light primary battery can be formed by arranging the anode catalyst on the outside of the conductive member by bending it in the opposite direction to the above, that is, with the metal on the inside.

前記重合体を筒状に屈曲形成することにより、例えば円筒形や角筒形の一次電池を形成することができる。この場合も、金属が外側となっても内側となってもどちらでも良い。 By bending the polymer into a tubular shape, for example, a cylindrical or rectangular tubular primary battery can be formed. In this case, either the outer side or the inner side of the metal may be used.

(削除) (Delete)

(削除) (Delete)

(削除) (Delete)

上記請求項の発明によれば、前記重合体を電気絶縁性の保護部材で保護したので、電池の損傷を防止すると共に電池自体の強度を向上させることができる。 According to the second aspect of the invention, since the polymer is protected by the electrically insulating protective member, the battery can be prevented from being damaged and the strength of the battery itself can be improved.

上記請求項の発明によれば、前記重合体を電気絶縁性の容器内に収納し、この容器に空気導入孔を設けたので、空気の供給を阻害することなく電池を十分保護することができる。 According to the third aspect of the present invention, since the polymer is housed in an electrically insulating container and the air introduction hole is provided in the container, the battery can be sufficiently protected without obstructing the supply of air. it can.

次に、本発明の実施形態について図面を参照しながら説明する。
図1は、本発明に係る酸性電解質を用いた電池の第1参考用実施形態を示すもので、(a)は概略斜視図、(b)は概略分解断面図である。
Next, embodiments of the present invention will be described with reference to the drawings.
FIG. 1 shows a first embodiment for reference of a battery using an acidic electrolyte according to the present invention, wherein (a) is a schematic perspective view, and (b) is a schematic exploded cross-sectional view.

図1において、1は負極となる板状の金属であり、本実施形態ではマグネシウムを用いるがこれに限定されない。この金属1としては、マグネシウム以外にアルミニウムを使用することができ、そのほか例えばリチウム、カルシウム、亜鉛、鉄、コバルト、カドミウム、鉛等も使用可能であると考えられる。又、金属1は金属粉を固めたものあるいは金属合金であっても使用することができる。この場合、金属1の大きさは3.5cm×3.5cm×0.4mm厚であり、重量は0.81gである。   In FIG. 1, reference numeral 1 denotes a plate-like metal serving as a negative electrode. In this embodiment, magnesium is used, but the present invention is not limited to this. As this metal 1, aluminum can be used in addition to magnesium. In addition, it is considered that lithium, calcium, zinc, iron, cobalt, cadmium, lead and the like can also be used. The metal 1 can be used even if it is a metal powder or a metal alloy. In this case, the size of the metal 1 is 3.5 cm × 3.5 cm × 0.4 mm thick, and the weight is 0.81 g.

2は金属1の下に配置するセパレータであり、合成樹脂等から形成されて陽イオンを通過できるようにしてある。このセパレータ2の大きさは4cm×4.5cm×0.1mm厚であり、重量は0.025gである。尚、このセパレータ2を設けないで実施することも可能である。   A separator 2 is disposed under the metal 1 and is formed of a synthetic resin or the like so that it can pass cations. The size of the separator 2 is 4 cm × 4.5 cm × 0.1 mm thick, and the weight is 0.025 g. It is also possible to carry out without providing this separator 2.

3はセパレータ2の下に配置する正極となる通気性の導電部材であり、この場合はカーボンシートが用いられ、大きさは4cm×3.5cm×0.3mm厚であり、重量は0.12gである。この導電部材3における前記セパレータ2に対向する面側(上側面)には酸性電解質4が塗布されている。この酸性電解質4は、ゲル化した酸性電解液が用いられているがそれに限定されず、例えば液体及び触媒と複合した酸性電解液、又はゲル及び触媒と複合した酸性電解液なども使用することができる。   Reference numeral 3 denotes a breathable conductive member serving as a positive electrode disposed under the separator 2. In this case, a carbon sheet is used, the size is 4 cm × 3.5 cm × 0.3 mm, and the weight is 0.12 g. It is. An acidic electrolyte 4 is applied to the surface side (upper side surface) of the conductive member 3 facing the separator 2. The acidic electrolyte 4 is a gelled acidic electrolytic solution, but is not limited thereto. For example, an acidic electrolytic solution combined with a liquid and a catalyst, or an acidic electrolytic solution combined with a gel and a catalyst may be used. it can.

前記導電部材3のセパレータ2に対向しない面側(下側面)には陽極触媒5を配置すると共に、この陽極触媒5に集電体6を取り付ける。この場合、陽極触媒5はカーボン粉末と触媒とを混合してペースト状に形成したものであり、この陽極触媒5を前記導電部材3の下側面に付着させると共に前記集電体6を取り付けることができる。又、予め集電体6に陽極触媒5を塗布して押し固めておき、この集電体6を前記導電部材の下面側に配置するようにしても良い。集電体6は、例えばカーボンで形成した細板状のものを用いることができ、その大きさは0.5cm×6.5cm×0.1cm厚であり、重量は0.36gである。尚、導電部材3に配線する場合には集電体6を設けなくても良い。   An anode catalyst 5 is disposed on the surface side (lower side surface) of the conductive member 3 not facing the separator 2, and a current collector 6 is attached to the anode catalyst 5. In this case, the anode catalyst 5 is a paste formed by mixing carbon powder and a catalyst. The anode catalyst 5 is attached to the lower surface of the conductive member 3 and the current collector 6 is attached. it can. Alternatively, the anode catalyst 5 may be applied to the current collector 6 and pressed in advance, and the current collector 6 may be disposed on the lower surface side of the conductive member. As the current collector 6, for example, a thin plate formed of carbon can be used, and the size thereof is 0.5 cm × 6.5 cm × 0.1 cm, and the weight is 0.36 g. Note that the current collector 6 may not be provided when wiring to the conductive member 3.

このようにして、負極となる金属1と、セパレータ2と、正極となる導電部材3とを重ね合わせて重合体7を形成し、導電部材3のセパレータ2に対向する面側には酸性電解質4が付着され、セパレータ2に対向しない面側には陽極触媒5を付着すると共に、この陽極触媒5に集電体6を取り付けることで小型・軽量の一次電池を形成することができる。
この場合、酸性電解質4としては過塩素酸(HClO)を用いるが、それに限定されない。
In this manner, the polymer 1 is formed by superimposing the metal 1 serving as the negative electrode, the separator 2 and the conductive member 3 serving as the positive electrode, and the acidic electrolyte 4 is formed on the surface of the conductive member 3 facing the separator 2. The anode catalyst 5 is attached to the surface side not facing the separator 2, and the current collector 6 is attached to the anode catalyst 5, whereby a small and light primary battery can be formed.
In this case, perchloric acid (HClO 4 ) is used as the acidic electrolyte 4, but is not limited thereto.

上記のような構成を備えた電池において、電池化学反応に伴って前記負極の金属1からマグネシウムイオンが溶出すると共に水素が発生し、図示しないリード線を介して電子が金属1から正極の導電部材3側に移動し、この導電部材3に供給される空気中の酸素が還元されて水を生成する。   In the battery having the above-described configuration, magnesium ions are eluted from the metal 1 of the negative electrode and hydrogen is generated in association with the battery chemical reaction, and electrons are transferred from the metal 1 to the positive electrode conductive member via a lead wire (not shown). The oxygen in the air supplied to the conductive member 3 is reduced and water is generated.

この電池化学反応により、前記酸性電解質4の過塩素酸はHと[ClOとに電離し、[ClOが金属1から生じるMg2+と結合して錯塩Mg(ClO2となる。この錯塩は金属1の表面に付着すると分極が生じて起電力を阻害するが、前記生成水によって簡単に溶解するため金属1への付着が抑えられる。このため、金属1の表面は殆ど清浄状態に保持されることから、常時確実に電池化学反応が得られると共に起電力の低下を抑えることができる。 By this battery chemical reaction, perchloric acid in the acidic electrolyte 4 is ionized into H + and [ClO 4 ] −, and [ClO 4 ] is combined with Mg 2+ generated from the metal 1 to form a complex salt Mg (ClO 4 ). 2 When this complex salt adheres to the surface of the metal 1, polarization occurs and inhibits electromotive force. However, since the complex salt is easily dissolved by the generated water, the adhesion to the metal 1 is suppressed. For this reason, since the surface of the metal 1 is almost kept clean, a battery chemical reaction can always be obtained reliably and a reduction in electromotive force can be suppressed.

従来の電解液の役割は、電池内の内部抵抗を低くして電極近傍での電気的中性を保つことであるが、本発明ではこの役割に加えて負極側の触媒機能を付加するために酸性電解質を用いたものである。又、酸性電解質を用いることで、アルカリ性電解質よりも安全性を高めることができる。   The role of the conventional electrolyte is to reduce the internal resistance in the battery and maintain electrical neutrality in the vicinity of the electrode. In the present invention, in addition to this role, in order to add a catalytic function on the negative electrode side An acidic electrolyte is used. Moreover, by using an acidic electrolyte, safety can be enhanced as compared with an alkaline electrolyte.

この一次電池は、負極の金属1にリード線(図略)の端部を固定し、集電体6の突出端部にもリード線(図略)の端部を取り付けて電池性能試験を行った。この電池性能試験においては、北斗電工株式会社製の充放電試験機(HJR−110mSM6)を使用し、前記リード線に接続して1mAの負荷を掛け、電圧が2.5Vから1Vに低下するまでの電気容量を計測した。この電気容量は、828.8mAh/gであり、前記従来のマグネシウム電池の電気容量は170mAh/g程度であるから、単純計算で約4.8倍であることが分かった。   In this primary battery, the end of the lead wire (not shown) is fixed to the metal 1 of the negative electrode, and the end of the lead wire (not shown) is also attached to the protruding end of the current collector 6 to perform a battery performance test. It was. In this battery performance test, a charge / discharge tester (HJR-110mSM6) manufactured by Hokuto Denko Co., Ltd. was used, connected to the lead wire, a load of 1 mA was applied, and the voltage decreased from 2.5V to 1V. The electric capacity of was measured. Since this electric capacity is 828.8 mAh / g and the electric capacity of the conventional magnesium battery is about 170 mAh / g, it was found that it was about 4.8 times by simple calculation.

図2は、本発明に係る酸性電解質を用いた電池の第2参考用実施形態を示すもので、(a)は概略斜視図、(b)は模式的概略断面図である。ここで、第1参考用実施形態と同じ構成要素は、前記と同じ符号をつけて詳しい説明は省略する。 2A and 2B show a second reference embodiment of a battery using an acidic electrolyte according to the present invention, in which FIG. 2A is a schematic perspective view, and FIG. 2B is a schematic schematic cross-sectional view. Here, the same components as those in the first reference embodiment are denoted by the same reference numerals as those described above, and detailed description thereof is omitted.

第2参考用実施形態では、負極となる金属1と、セパレータ2と、正極となる導電部材3とを重ね合わせて重合体7を形成し、導電部材3のセパレータ2に対向する面側には酸性電解質4が付着され、重合体7を金属1が外側面となるようにして二つに折り曲げ、導電部材3の内側面に生じた空間部に陽極触媒5を配置すると共に、この陽極触媒5に集電体6を取り付けた構成である。前記第1参考用実施形態が平面型の電池であるのに対し、第2参考用実施形態は折曲型の電池である点で相違している。 In the second reference embodiment, the polymer 1 is formed by superimposing the metal 1 serving as the negative electrode, the separator 2 and the conductive member 3 serving as the positive electrode, and the conductive member 3 has a surface facing the separator 2. The acidic electrolyte 4 is attached, the polymer 7 is folded in half so that the metal 1 becomes the outer surface, and the anode catalyst 5 is disposed in the space formed on the inner surface of the conductive member 3. It is the structure which attached the collector 6 to. The first reference embodiment is a flat type battery, whereas the second reference embodiment is a bent type battery.

この第2参考用実施形態では、重合体7を二つ折りする際に金属1が外側面となるようにしたが、これに限定されずに金属1が内側面となるように二つ折りして実施することも可能である。その場合には、図示は省略したが導電部材3の外側面に陽極触媒5を付着すると共に、この陽極触媒5に集電体6を取り付ける。 In the second reference embodiment, when the polymer 7 is folded in half, the metal 1 becomes the outer surface. However, the present invention is not limited to this, and the metal 1 is folded in half so that the metal 1 becomes the inner surface. It is also possible to do. In that case, although not shown, the anode catalyst 5 is attached to the outer surface of the conductive member 3, and the current collector 6 is attached to the anode catalyst 5.

図3は、本発明に係る酸性電解質を用いた電池の第3参考用実施形態を示す模式的概略断面図である。ここでも、第1参考用実施形態と同じ構成要素は、前記と同じ符号をつけて詳しい説明は省略する。 FIG. 3 is a schematic schematic cross-sectional view showing a third reference embodiment of the battery using the acidic electrolyte according to the present invention. Again, the same components as those in the first reference embodiment are denoted by the same reference numerals as those described above, and detailed description thereof is omitted.

この第3参考用実施形態では、負極となる金属1と、セパレータ2と、正極となる導電部材3とを重ね合わせて重合体7を形成し、導電部材3のセパレータ2に対向する面側には酸性電解質4が付着され、重合体7を金属1が外側面となるようにして円筒状に屈曲し、導電部材3の内側面に生じた円形の空間部に陽極触媒5を配置すると共に、この陽極触媒5に集電体6を取り付けた構成である。 In this third embodiment for reference, the polymer 1 is formed by superimposing the metal 1 serving as the negative electrode, the separator 2 and the conductive member 3 serving as the positive electrode on the surface of the conductive member 3 facing the separator 2. Has an acidic electrolyte 4 attached, bends the polymer 7 in a cylindrical shape with the metal 1 as an outer surface, and disposes the anode catalyst 5 in a circular space formed on the inner surface of the conductive member 3, The current collector 6 is attached to the anode catalyst 5.

この場合は、重合体7を円筒状に屈曲する際に金属1が外側面となるようにしたが、これに限定されずに金属1が内側面となるように円筒状に屈曲して実施することも可能である。その時には、図示は省略したが導電部材3の外側面に陽極触媒5を付着すると共に、この陽極触媒5に集電体6を取り付ける。   In this case, when the polymer 7 is bent into a cylindrical shape, the metal 1 becomes the outer surface, but the present invention is not limited to this, and the bending is performed in a cylindrical shape so that the metal 1 becomes the inner surface. It is also possible. At that time, although not shown, the anode catalyst 5 is attached to the outer surface of the conductive member 3, and the current collector 6 is attached to the anode catalyst 5.

又、上記第3参考用実施形態では円筒状に屈曲する場合であったが、これに限定されることなく角筒状に形成することも可能であり、例えば三角形状や、四角形状その他の角形にすることができる。更に、円筒状の場合は円形に限定されずに、楕円形であっても良い。 Further, in the third embodiment for reference, it is a case of bending into a cylindrical shape, but it is not limited to this, and it can also be formed into a rectangular tube shape, for example, a triangular shape, a rectangular shape or other rectangular shapes. Can be. Furthermore, in the case of a cylindrical shape, it is not limited to a circular shape and may be an elliptical shape.

図4は、本発明に係る酸性電解質を用いた電池の第4参考用実施形態を示す概略分解断面図である。ここにおいても、第1参考用実施形態と同じ構成要素は、前記と同じ符号をつけて詳しい
説明は省略する。
FIG. 4 is a schematic exploded sectional view showing a fourth reference embodiment of the battery using the acidic electrolyte according to the present invention. Also in this case, the same components as those in the first reference embodiment are denoted by the same reference numerals as those described above, and detailed description thereof is omitted.

この第4参考用実施形態では、第1参考用実施形態と基本的な構成は同じであり、負極となる金属1と、セパレータ2と、正極となる導電部材3とを重ね合わせて重合体7を形成し、導電部材3のセパレータ2に対向する面側には酸性電解質4が付着され、セパレータ2に対向しない面側には陽極触媒5を付着すると共に、この陽極触媒5に集電体6を取り付けた構成であり、金属1とセパレータ2との間に吸水・保湿部材8を配置したことを特徴とする二次電池である。吸水・保湿部材8は、液体を吸収して湿潤状態に保持できる機能を有するものであり、この場合はガラス繊維シートが用いられているが、これに限定されず例えば紙、布、不織布や吸水性樹脂等を使用することができる。尚、前記参考用実施形態1〜3の一次電池においても、金属1とセパレータ2との間に吸水・保湿部材8を配置させることもある。吸水・保湿部材8を配置することにより、金属1に対して酸性電解質4を確実に且つ均等に接触させることができ、安定した起電力を得ることが可能となる。 In the fourth reference embodiment, the basic configuration is the same as that of the first reference embodiment. The polymer 7 is formed by superimposing the metal 1 serving as the negative electrode, the separator 2, and the conductive member 3 serving as the positive electrode. The acidic electrolyte 4 is attached to the surface of the conductive member 3 that faces the separator 2, and the anode catalyst 5 is attached to the surface that does not face the separator 2, and the current collector 6 is attached to the anode catalyst 5. The secondary battery is characterized in that a water absorbing / moisturizing member 8 is disposed between the metal 1 and the separator 2. The water absorption / moisture retention member 8 has a function of absorbing liquid and maintaining the wet state. In this case, a glass fiber sheet is used, but the present invention is not limited to this. Resin etc. can be used. In the primary batteries of Reference Embodiments 1 to 3, the water absorption / humidity retention member 8 may be disposed between the metal 1 and the separator 2. By disposing the water absorbing / moisturizing member 8, the acidic electrolyte 4 can be reliably and evenly brought into contact with the metal 1, and a stable electromotive force can be obtained.

電池化学反応に伴って、前記負極の金属1は徐々に溶け出して減少する。この金属1が溶滅すると電池化学反応が停止して、前記一次電池はそれ以上使用できなくなる。しかしながら、第4実施形態において、負極の金属1が溶滅した際に新品の金属に取り替えることで、継続して使用することが可能となる。即ち、二次電池としての使用が可能となり、しかも従来の二次電池のように外部電源に接続して充電する必要はない。   With the battery chemical reaction, the metal 1 of the negative electrode gradually melts and decreases. When the metal 1 is melted, the battery chemical reaction stops and the primary battery can no longer be used. However, in the fourth embodiment, when the metal 1 of the negative electrode is melted, it can be continuously used by replacing it with a new metal. That is, it can be used as a secondary battery, and it is not necessary to charge the battery by connecting it to an external power source unlike a conventional secondary battery.

図5は、本発明に係る酸性電解質を用いた電池の第実施形態を示す模式的概略断面図である。この場合も、第1参考用実施形態と同じ構成要素は、前記と同じ符号をつけて詳しい説明は省略する。 FIG. 5 is a schematic schematic cross-sectional view showing a first embodiment of a battery using an acidic electrolyte according to the present invention. Also in this case, the same components as those in the first reference embodiment are denoted by the same reference numerals as those described above, and detailed description thereof is omitted.

この第実施形態では、第1参考用実施形態と基本的な構成は同じであり、負極となる金属1と、セパレータ2と、正極となる導電部材3とを重ね合わせて重合体7を形成し、導電部材3のセパレータ2に対向する面側には酸性電解質4が付着され、セパレータ2に対向しない面側には陽極触媒5を付着すると共に、この陽極触媒5に集電体6を取り付け、金属1とセパレータ2との間に吸水・保湿部材8を配置してあり、この吸水・保湿部材8に金属1を取り付ける点に特徴を有している。 In this first embodiment, the basic configuration is the same as that of the first reference embodiment, and the polymer 1 is formed by superimposing the metal 1 serving as the negative electrode, the separator 2, and the conductive member 3 serving as the positive electrode. The acidic electrolyte 4 is attached to the surface of the conductive member 3 facing the separator 2, the anode catalyst 5 is attached to the surface of the conductive member 3 not facing the separator 2, and the current collector 6 is attached to the anode catalyst 5. The water absorbing / moisturizing member 8 is disposed between the metal 1 and the separator 2, and the metal 1 is attached to the water absorbing / moisturizing member 8.

このようにして、金属1が吸水・保湿部材8に取り付けられていると、負極の金属1が溶滅した際に図5のように金属1を吸水・保湿部材8と一緒に綺麗に剥ぎ取って取り替えることができる。吸水・保湿部材8とその下のセパレータ2とは非接着であるから、吸水・保湿部材8を剥がす作業は容易に行うことができる。これにより、溶滅した金属1の残渣が残留することなく完全に取り除かれるので、重合体7は綺麗な状態で残される。このため、新しい吸水・保湿部材と共に金属1を取り替える作業がきわめて容易になる。この時、新たなガラス繊維シートを省いて新品の金属だけ取り替えるようにしても良い。   In this way, when the metal 1 is attached to the water absorbing / moisturizing member 8, when the metal 1 of the negative electrode is melted, the metal 1 is peeled off together with the water absorbing / humidifying member 8 as shown in FIG. Can be replaced. Since the water absorbing / moisturizing member 8 and the separator 2 thereunder are not bonded, the work of peeling off the water absorbing / humidifying member 8 can be easily performed. Thereby, the melted metal 1 residue is completely removed without remaining, so that the polymer 7 is left in a clean state. For this reason, the operation | work which replaces the metal 1 with a new water absorption and moisture retention member becomes very easy. At this time, a new glass fiber sheet may be omitted and only a new metal may be replaced.

図6は、本発明に係る酸性電解質を用いた電池の第実施形態を示す概略側面図である。これは、前記平面型電池(図1)や折曲型電池(図2)を、電気絶縁性の保護部材9で挟み付けて保護した構成である。これにより、重合体7を損傷から保護できると共に、重合体7の強度を向上させることができる。保護部材9としては、例えばアクリル等の合成樹脂板を使用することができ、上下の保護部材9をボルトとナット等の適宜の締着具10で固定する。尚、重合体7の保護手段はこれに限定されない。 FIG. 6 is a schematic side view showing a second embodiment of a battery using an acidic electrolyte according to the present invention. This is a configuration in which the planar battery (FIG. 1) and the folded battery (FIG. 2) are sandwiched and protected by an electrically insulating protective member 9. Thereby, while being able to protect the polymer 7 from damage, the intensity | strength of the polymer 7 can be improved. As the protection member 9, for example, a synthetic resin plate such as acrylic can be used, and the upper and lower protection members 9 are fixed with appropriate fasteners 10 such as bolts and nuts. In addition, the protection means of the polymer 7 is not limited to this.

図7は、本発明に係る酸性電解質を用いた電池の第実施形態を示す概略斜視図である。これは、前記平面型電池(図1)や折曲型電池(図2)を、電気絶縁性の容器11内に収納したものである。これにより、重合体7を損傷から保護できると共に、重合体7の強度を向上させることができる。この容器11は例えばアクリル等の合成樹脂で形成することができ、空気導入孔11aを設けると共に集電体6の取出孔11bをそれぞれ設ける。空気導入孔11aは図示の窓孔に限定されず、電池への空気供給を十分できる形態であれば良く、例えば複数の小孔で構成するようにしても良い。 FIG. 7 is a schematic perspective view showing a third embodiment of the battery using the acidic electrolyte according to the present invention. This is one in which the planar battery (FIG. 1) and the folded battery (FIG. 2) are housed in an electrically insulating container 11. Thereby, while being able to protect the polymer 7 from damage, the intensity | strength of the polymer 7 can be improved. The container 11 can be formed of, for example, a synthetic resin such as acrylic, and is provided with an air introduction hole 11 a and an extraction hole 11 b of the current collector 6. The air introduction hole 11a is not limited to the illustrated window hole, and may have any form that can sufficiently supply air to the battery. For example, the air introduction hole 11a may be composed of a plurality of small holes.

前記の筒型電池(図3)の場合は、図示は省略したが電気絶縁性の筒状容器を用いて、この筒状容器内に重合体を収納する構成にすれば良い。角筒状の場合は、この角筒状に対応する容器を用いるようにする。   In the case of the cylindrical battery (FIG. 3), although not shown, an electrically insulating cylindrical container may be used to store the polymer in the cylindrical container. In the case of a rectangular tube shape, a container corresponding to this rectangular tube shape is used.

本発明に係る酸性電解質を用いた電池は、例えばノートパソコン、携帯電話、時計、電気器具、電動工具等の各種機器のバッテリーとして利用することができ、その他電気自動車、家庭用発電ユニット、無停電電源、医療機器等広い範囲での用途が期待できる。   The battery using the acidic electrolyte according to the present invention can be used as a battery for various devices such as notebook computers, mobile phones, watches, electric appliances, electric tools, etc. Applications in a wide range such as power supplies and medical equipment can be expected.

本発明に係る酸性電解質を用いた電池の第1参考用実施形態を示すもので、(a)は概略斜視図、(b)は概略分解断面図である。BRIEF DESCRIPTION OF THE DRAWINGS The 1st embodiment for reference of the battery using the acidic electrolyte which concerns on this invention is shown, (a) is a schematic perspective view, (b) is a schematic exploded sectional view. 本発明に係る酸性電解質を用いた電池の第2参考用実施形態を示すもので、(a)は概略斜視図、(b)は模式的概略断面図である。The 2nd embodiment for reference of the battery using the acidic electrolyte which concerns on this invention is shown, (a) is a schematic perspective view, (b) is typical schematic sectional drawing. 本発明に係る酸性電解質を用いた電池の第3参考用実施形態を示す模式的概略断面図である。It is a typical schematic sectional drawing which shows 3rd embodiment for reference of the battery using the acidic electrolyte which concerns on this invention. 本発明に係る酸性電解質を用いた電池の第4参考用実施形態を示す概略分解断面図である。It is a general | schematic exploded sectional view which shows 4th embodiment for reference of the battery using the acidic electrolyte which concerns on this invention. 本発明に係る酸性電解質を用いた電池の第実施形態を示す模式的概略断面図である。It is a typical schematic sectional view showing a 1st embodiment of a battery using an acidic electrolyte concerning the present invention. 本発明に係る酸性電解質を用いた電池の第実施形態を示す概略側面図である。It is a schematic side view which shows 2nd Embodiment of the battery using the acidic electrolyte which concerns on this invention. 本発明に係る酸性電解質を用いた電池の第実施形態を示す概略斜視図である。It is a schematic perspective view which shows 3rd Embodiment of the battery using the acidic electrolyte which concerns on this invention.

1 金属
2 セパレータ
3 導電部材
4 酸性電解質
5 陽極触媒
6 集電体
7 重合体
8 吸水・保湿部材
9 保護部材
10 締着具
11 容器
11a 空気導入孔
11b 取出孔
DESCRIPTION OF SYMBOLS 1 Metal 2 Separator 3 Conductive member 4 Acid electrolyte 5 Anode catalyst 6 Current collector 7 Polymer 8 Water absorption / humidity retention member 9 Protection member 10 Fastening tool 11 Container 11a Air introduction hole 11b Extraction hole

Claims (3)

少なくとも負極となる金属と、正極となる導電部材とを、前記金属と導電部材との間にセパレータを配置し、前記金属とセパレータとの間に吸水・保湿部材を配置して、重ね合わせて重合体を形成し、前記導電部材における前記金属に対向する側には酸性電解質が付着され、前記金属に対向しない側には陽極触媒を配置して成る酸性電解質を用いた電池であって、
前記吸水・保湿部材に前記金属を取り付け、当該吸水・保湿部材と共に前記金属を交換することを特徴とする酸性電解質を用いた電池。
At least a metal serving as a negative electrode and a conductive member serving as a positive electrode are overlapped with a separator disposed between the metal and the conductive member, and a water absorbing / moisturizing member disposed between the metal and the separator. A battery using an acidic electrolyte formed by forming an union and having an acidic electrolyte attached to a side of the conductive member facing the metal and a side not facing the metal ;
A battery using an acidic electrolyte , wherein the metal is attached to the water absorption / humidity retention member and the metal is exchanged together with the water absorption / humidity retention member .
前記重合体を電気絶縁性の保護部材で保護したことを特徴とする請求項1記載の酸性電解質を用いた電池。 Battery using an acidic electrolyte according to claim 1 Symbol mounting, characterized in that protected the polymer with a protective member of electrical insulation. 前記重合体を電気絶縁性の容器内に収納し、この容器に空気導入孔を設けたことを特徴とする請求項1又は請求項2記載の酸性電解質を用いた電池。 The polymer was housed in an electrically insulating vessel with claim 1 or claim 2 Symbol placement of acidic electrolyte is characterized by providing an air introduction hole in the container cell.
JP2008228407A 2008-09-05 2008-09-05 Batteries using acidic electrolyte Active JP5385570B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008228407A JP5385570B2 (en) 2008-09-05 2008-09-05 Batteries using acidic electrolyte

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008228407A JP5385570B2 (en) 2008-09-05 2008-09-05 Batteries using acidic electrolyte

Publications (2)

Publication Number Publication Date
JP2010062074A JP2010062074A (en) 2010-03-18
JP5385570B2 true JP5385570B2 (en) 2014-01-08

Family

ID=42188642

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008228407A Active JP5385570B2 (en) 2008-09-05 2008-09-05 Batteries using acidic electrolyte

Country Status (1)

Country Link
JP (1) JP5385570B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20200000517A (en) * 2018-06-22 2020-01-03 선광엘티아이(주) Metal air battery Systems that can be mounted on small vehicles

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013054418A1 (en) * 2011-10-13 2013-04-18 トヨタ自動車株式会社 Air cell, mobile body comprising air cell, and use of air cell
JPWO2014126204A1 (en) * 2013-02-15 2017-02-02 エイディシーテクノロジー株式会社 Air battery
JP5891569B2 (en) * 2014-04-02 2016-03-23 ワイティーエス・サイエンス・プロパティーズ・プライベート・リミテッド Magnesium fuel body, magnesium air battery, and electronic device
JP6454824B1 (en) * 2017-09-28 2019-01-16 マクセルホールディングス株式会社 Sheet air battery and patch

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5590080A (en) * 1978-12-27 1980-07-08 Toshiba Battery Co Ltd Air cell
JPS5590081A (en) * 1978-12-27 1980-07-08 Toshiba Battery Co Ltd Air cell
JPS55157875A (en) * 1979-05-25 1980-12-08 Toshiba Battery Co Ltd Small-size air cell
JPS5650071A (en) * 1979-09-28 1981-05-07 Toshiba Battery Co Ltd Air cell
JPH0745270A (en) * 1993-07-30 1995-02-14 Electric Fuel Efl Ltd Zinc-battery anode and its manufacture
JP2001043864A (en) * 1999-07-29 2001-02-16 Sony Corp Cylindrical air electrode and cylindrical air battery
JP3764623B2 (en) * 2000-03-27 2006-04-12 株式会社東芝 Oxygen lithium secondary battery
JP4296114B2 (en) * 2003-03-28 2009-07-15 株式会社東芝 Air battery
JP4278468B2 (en) * 2003-09-11 2009-06-17 孝止 安東 Battery positive electrode material and air battery using the same
JP4955707B2 (en) * 2006-02-17 2012-06-20 イー.エム.ダブリュ.エナジー カンパニー リミテッド Cylindrical zinc-air battery and method for manufacturing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20200000517A (en) * 2018-06-22 2020-01-03 선광엘티아이(주) Metal air battery Systems that can be mounted on small vehicles
KR102554406B1 (en) 2018-06-22 2023-07-12 선광엘티아이(주) Metal air battery Systems that can be mounted on small vehicles

Also Published As

Publication number Publication date
JP2010062074A (en) 2010-03-18

Similar Documents

Publication Publication Date Title
US8236463B2 (en) Magnetic current collector
AU2014307611B2 (en) Novel flow battery and usage thereof
US20130101878A1 (en) Battery comprising cuboid cells which contain a bipolar electrode
JP2006040875A (en) Electrode assembly and lithium secondary battery using it
JP6869280B2 (en) Coin-type secondary battery charge / discharge device
JP2007280831A (en) Power supply device
JP5385570B2 (en) Batteries using acidic electrolyte
JP5385569B2 (en) Batteries using acidic electrolyte
CN208298952U (en) Battery and electronic equipment
KR20190037786A (en) Battery module and battery pack including the same
KR101123636B1 (en) Cartridge seperate type metal-air battery
JP5660086B2 (en) Magnesium secondary battery
JP5406486B2 (en) Metal fuel cell
JP2008042003A (en) Lithium ion accumulation element
CN109565070A (en) Rechargeable battery
EP3641045A1 (en) Cable type battery
JP2020077528A (en) Fixture and storage battery module
KR20160037350A (en) Battery cell and device comprising thereof
JP2009151977A (en) Coin type secondary battery
KR20160041645A (en) Jelly roll type electrode assembly for secondary battery
KR20210060239A (en) Battery module, battery pack and vehicle comprising the same
JP6334361B2 (en) Power storage module
KR101760985B1 (en) Polymer battery
JP2011154914A (en) Power generation element
CN209896196U (en) Binary high-nickel battery

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20110901

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20130625

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20130812

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20130910

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20131004

R150 Certificate of patent or registration of utility model

Ref document number: 5385570

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250