JPH0686864B2 - Sealed mechanochemical element - Google Patents
Sealed mechanochemical elementInfo
- Publication number
- JPH0686864B2 JPH0686864B2 JP25537085A JP25537085A JPH0686864B2 JP H0686864 B2 JPH0686864 B2 JP H0686864B2 JP 25537085 A JP25537085 A JP 25537085A JP 25537085 A JP25537085 A JP 25537085A JP H0686864 B2 JPH0686864 B2 JP H0686864B2
- Authority
- JP
- Japan
- Prior art keywords
- mechanochemical
- sealed
- mechanochemical element
- acidity
- electrode
- 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 - Fee Related
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- Prostheses (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は、溶液中の酸性度を変えることにより可逆的に
伸縮させることができ、ロボット,義足,義手,人工心
臓,ケミカルエンジン,スイッチ,センサおよびプレ
ス,ジャッキなどの力源として、広い産業分野で利用で
きるメカノケミカル素子に関する。TECHNICAL FIELD The present invention can reversibly expand and contract by changing the acidity in a solution, and can be used for robots, artificial legs, artificial hands, artificial hearts, chemical engines, switches, sensors, and The present invention relates to a mechanochemical element that can be used in a wide range of industrial fields as a power source for presses and jacks.
従来の技術 化学エネルギーを直接機械エネルギーに変換できるメカ
ノケミカル反応は、小型,軽量,高効率,柔軟性,低公
害などの特徴のために、ロボットの人工筋肉や義足,人
工心臓などの医用機器などに非常に有望と考えられ、研
究開発が活発に行なわれるようになった。現在のとこ
ろ、有機高分子材料より作成した不溶性ゲルが最も応答
性がよく、酸性度,塩濃度,電気,光,熱などの入力に
対する伸縮が調べられている。たとえば、ポリメタクリ
ル酸とポリビニルアルコールを一部重合させて不溶化し
たゲルは、酸性度の変化によって、伸縮率20〜35%,応
答速度数分,引張強さは自重の約1000倍などの特性が得
られている。そのほかに生体物質であるコラーゲンで
は、塩濃度の変化で同様な特性が得られていて、コラー
ゲン繊維の伸縮を利用したケミカルエンジン(USP.3,32
1,907)が試作されている。Conventional technology The mechanochemical reaction that can directly convert chemical energy into mechanical energy is characterized by its small size, light weight, high efficiency, flexibility, low pollution, and other medical devices such as artificial muscles and artificial legs of robots and artificial hearts. It was thought to be very promising, and research and development became active. At present, insoluble gels made of organic polymer materials have the highest responsiveness, and expansion and contraction with respect to inputs such as acidity, salt concentration, electricity, light, and heat have been investigated. For example, a gel in which polymethacrylic acid and polyvinyl alcohol are partially polymerized and insolubilized has properties such as a stretching rate of 20 to 35%, a response speed of several minutes, and a tensile strength of about 1000 times its own weight due to changes in acidity. Has been obtained. In addition, collagen, which is a biological substance, has similar characteristics with changes in salt concentration. A chemical engine (USP.3,32) that utilizes expansion and contraction of collagen fibers
1,907) has been prototyped.
発明が解決しようとする問題点 ところで、酸性度の変化を得る手段として、水の電気分
解による方法がある。下に示す反応式により、陽極では
酸素ガスを発生しながら酸性となり、陰極では水素ガス
を発生しながらアルカリ性となり、いずれの電極から
も、通電電気量に比例して酸素や水素ガスの発生があ
る。このため、メカノケミカル素子を密閉とすることが
不可能であり、実用的観点から問題となる。さらにガス
の放出により水の減少が生じ、補水の必要が生ずる。Problems to be Solved by the Invention By the way, as a means for obtaining a change in acidity, there is a method by electrolysis of water. According to the reaction formula shown below, the anode becomes acidic while generating oxygen gas, and the cathode becomes alkaline while generating hydrogen gas, and oxygen and hydrogen gas are generated from any of the electrodes in proportion to the amount of electricity supplied. . Therefore, it is impossible to seal the mechanochemical element, which is a problem from a practical point of view. In addition, the release of gas causes a decrease in water and the need to replenish water.
陽極 2H2O→O2+4H++4e ……(1) E0=1.228−0.0591pH 陰極 4H2O+4e→2H2+4OH- ……(2) E0=0−0.0591pH 問題点を解決するための手段 電気化学反応として、下記のような金属の酸化還元反応
を用いて溶液の酸性度を可逆的に変化させる。すなわち
(1)式(2)式の代りに(3)式,(4)式の反応を
用いる。Anode 2H 2 O → O 2 + 4H + + 4e ...... (1) E 0 = 1.228-0.0591pH cathode 4H 2 O + 4e → 2H 2 + 4OH - ...... (2) E 0 = 0-0.0591pH to solve the problem Means As an electrochemical reaction, the acidity of the solution is reversibly changed by using a metal redox reaction as described below. That is, the reactions of the equations (3) and (4) are used instead of the equations (1) and (2).
Hg+H2O=HgO+2H++2e ……(3) HgO+H2O+2e=Hg+2OH- ……(4) このように酸素や水素ガス発生することなく、H+やOH-
を作成して酸性度を変えることができる。Hg + H 2 O = HgO + 2H ++ 2e …… (3) HgO + H 2 O + 2e = Hg + 2OH − …… (4) In this way, H + and OH − without generating oxygen or hydrogen gas.
Can be created to change the acidity.
なお、この場合、酸性およびアルカリ性で金属酸化物や
金属などの反応物質が溶解するとイオン交換膜を用いる
必要が生ずるので好ましくない。また当然のことながら
酸素,水素の発生反応より先にこれらの反応が起こる必
要があるので、標準酸化還元電位が0と1.228V VS.NHE
の間にあることなどが必要条件となる。In this case, it is not preferable because it is necessary to use an ion exchange membrane when acidic and alkaline reactants such as metal oxides and metals are dissolved. As a matter of course, since these reactions need to occur before the oxygen and hydrogen generation reactions, the standard redox potentials are 0 and 1.228V VS.NHE.
It is a necessary condition to be in between.
これらの条件を満たす電気化学反応系として上記のHg/H
gOのほかにHg/Hg(OH)2,Pd/Pd(OH)2,Pt/PtOなどがあ
る。これらの系の陽極での反応式と標準酸化還元電位お
よび酸性度による電位の変化を示す。As an electrochemical reaction system that satisfies these conditions, the above Hg / H
In addition to gO, there are Hg / Hg (OH) 2 , Pd / Pd (OH) 2 , Pt / PtO. The reaction formulas at the anode of these systems and the standard redox potential and the potential change due to acidity are shown.
Hg+2H2O=Hg(OH)2+2H++2e E0=1.034−0.0591pH Pd+H2O=PdO+2H++2e E0=0.897−0.0591pH Pt+H2O=PtO+2H++2e E0=0.980−0.0591pH なお、上記のHg/HgOの(3)式の平衡電位はつぎのとお
りである。 Hg + 2H 2 O = Hg ( OH) 2 + 2H + + 2e E 0 = 1.034-0.0591pH Pd + H 2 O = PdO + 2H + + 2e E 0 = 0.897-0.0591pH Pt + H 2 O = PtO + 2H + + 2e E 0 = 0.980-0.0591pH The above The equilibrium potential of Eq. (3) for Hg / HgO is as follows.
E0=0.926−0.0591pH 作用 これらの電気化学反応を用いてガスの発生がなくて酸性
度を可逆的に変化させることができるので、密閉式の素
子を作ることが可能となる。そのため、保守容易で取扱
い容易な人工筋肉,メカノケミカル素子とすることがで
きる。E 0 = 0.926-0.0591 pH action Since these electrochemical reactions can be used to reversibly change the acidity without the generation of gas, it is possible to make a sealed device. Therefore, an artificial muscle and a mechanochemical element that can be easily maintained and handled can be provided.
実施例 まずポリメタクリル酸(分子量約8000)の3重量%水溶
液とポリビニルアルコール(分子量約1800)の3重量%
水溶液とを重量比1:3の割合で混合し、この混合物10cm3
を、直径12cmのシャーレの中に入れ、約45℃で乾燥後、
容器より剥離し、幅5mm,長さ70mmに切断した。厚さは約
30μmであった。その後、約115℃に約2時間保って重
合させて不溶性とした。このようなフィルムを80枚製作
し束ねた後、水に浸漬して膨潤させた。これを長さ約10
cm,直径10mmのゴム製チューブ内に充填した。ついで、
この両端に、酸化水銀(HgO)と水銀を各0.4g含んだ酸
化水銀電極を挿入した。そして、チューブの両端を、上
記フィルムの束と電極を結びつけた状態で封口し、ゴム
チューブ外に液が漏れないようにした。Example First, a 3 wt% aqueous solution of polymethacrylic acid (molecular weight of about 8000) and 3 wt% of polyvinyl alcohol (molecular weight of about 1800)
Mix with the aqueous solution in a weight ratio of 1: 3, and mix this mixture with 10 cm 3
Put in a petri dish with a diameter of 12 cm, and dried at about 45 ° C.
It was peeled from the container and cut into a width of 5 mm and a length of 70 mm. Thickness is about
It was 30 μm. Then, the mixture was kept at about 115 ° C. for about 2 hours to polymerize it to make it insoluble. Eighty such films were produced, bundled, and then immersed in water to swell. This is about 10
It was filled in a rubber tube having a diameter of 10 cm and a diameter of 10 mm. Then,
Mercury oxide electrodes containing 0.4 g each of mercury oxide (HgO) and mercury were inserted at both ends. Then, both ends of the tube were sealed in a state where the bundle of films and the electrodes were connected to each other so that the liquid did not leak to the outside of the rubber tube.
なお、酸化水銀電極の製法は、電極芯材として白金線
(0.2φ)を用い、フッ素樹脂ディスパーションを結着
剤として約3%加え、乾燥後500Kg/cm3のプレス圧で成
型した。大きさ3mm×10mm,厚さ約2mmであり、酸化およ
び還元方向とも,理論充てん容量は200mAhとなった。The mercury oxide electrode was manufactured by using a platinum wire (0.2φ) as the electrode core material, adding about 3% of fluororesin dispersion as the binder, and drying and molding at a pressing pressure of 500 kg / cm 3 . The size was 3 mm × 10 mm and the thickness was about 2 mm, and the theoretical filling capacity was 200 mAh in both the oxidation and reduction directions.
第1図には中央部から折り曲げてバイメタル形状とし通
電によって中央部が左右に移動することを観察するため
の素子の断面概略図を示す。また第2図には素子の両端
を固定し、通電によって中央部に固定した金具が移動す
ることを観察するための素子の断面概略図である。図中
1と3はHg/HgO電極、2と4はこれらの電極端子、5は
上記の伸縮フィルム、6はゴム製外ケース、7は外ケー
スに固定した中央部金具であり、8は0.05Mの塩化ナト
リウム溶液の電解液である。FIG. 1 shows a schematic cross-sectional view of an element for observing that the central portion moves left and right by energization by bending it from the central portion to form a bimetal shape. Further, FIG. 2 is a schematic cross-sectional view of the element for fixing both ends of the element and observing that the metal fitting fixed to the central portion moves by energization. In the figure, 1 and 3 are Hg / HgO electrodes, 2 and 4 are these electrode terminals, 5 is the elastic film, 6 is a rubber outer case, 7 is a central metal fitting fixed to the outer case, and 8 is 0.05. Electrolyte solution of M sodium chloride solution.
両電極間に直流電圧を約3V印加し、第1図に示すバイメ
タル形状の素子の先端の回転角度変化と第2図に示す素
子の中央部金具の移動の速度を測定し、結果を第3図の
曲線AとBにそれぞれ示す。曲線Aより、左30゜から右
30゜までの60゜を約5分間で回転することが分かる。一
方曲線Bより、中央部は左右に10mm、すなわち合計20mm
の移動を示した。これは繰り返すことが可能であり、こ
の間、電流は2〜20mAと規則的に変化した。A direct current voltage of about 3 V was applied between both electrodes, and the change in the rotation angle of the tip of the bimetal-shaped element shown in FIG. 1 and the movement speed of the central metal part of the element shown in FIG. 2 were measured. Curves A and B are shown in the figure respectively. From curve A, left 30 ° to right
It turns out that 60 ° up to 30 ° rotates in about 5 minutes. On the other hand, from curve B, the central part is 10mm to the left and right, that is, 20mm in total.
Showed the move. This can be repeated, during which the current changed regularly between 2 and 20 mA.
以上の実施例はHg/HgO電極を両電極に用いた場合であっ
たが、上に示す電極反応のいずれを用いても密閉が可能
であり、また他のメカノケミカル材料でも同様な効果が
生じた。さらに、本実施例よりさらに電極を大きくする
か、あるいは中心部のみ残して電極とすると応答時間は
一層速くすることができた。The above example was the case where Hg / HgO electrodes were used for both electrodes, but it is possible to seal using any of the electrode reactions shown above, and similar effects occur with other mechanochemical materials. It was Furthermore, the response time could be further shortened by making the electrode larger than that of this example, or by leaving only the central portion and using the electrode.
発明の結果 以上のように、メカノケミカル素子の密閉化ができたの
で、従来の開放式にくらべ取り扱いを容易とすることが
可能となり、本素子の実用化に向けて前進することがで
きた。As a result of the invention, since the mechanochemical element can be hermetically sealed as described above, it becomes possible to handle the element easily compared with the conventional open type, and it has been possible to advance to the practical application of this element.
第1図及び第2図は本発明のメカノケミカル素子の実施
例を示す縦断面略図、第3図はこれら素子の性能を示す
図である。 1,3……Hg/HgO電極、2,4……端子、5……伸縮フィル
ム、6……ゴム製外ケース、7……中央部金具、8……
電解液。1 and 2 are schematic longitudinal sectional views showing examples of the mechanochemical element of the present invention, and FIG. 3 is a view showing the performance of these elements. 1,3 …… Hg / HgO electrodes, 2,4 …… Terminals, 5 …… Stretch film, 6 …… Rubber outer case, 7 …… Center part metal fittings, 8 ……
Electrolyte.
Claims (3)
れ電極を配置し、上記外ケース内に溶液の酸性度の変化
によって可逆的に伸縮する不溶性高分子と電解液を充満
し、直流電気入力による酸性度の変化によって伸縮応答
するメカノケミカル素子において、両電極にHg/HgO,Hg/
Hg(OH)2,Pd/Pd(OH)2およびPt/PtOの電極反応のう
ち少なくとも1つを用いることを特徴とする密閉式メカ
ノケミカル素子。1. An electrode is disposed inside both ends of a stretchable outer case, and the outer case is filled with an insoluble polymer that expands and contracts reversibly according to a change in the acidity of the solution and an electrolytic solution. In a mechanochemical element that responds to expansion and contraction due to changes in acidity due to input, Hg / HgO, Hg /
A sealed mechanochemical element characterized by using at least one of the electrode reactions of Hg (OH) 2 , Pd / Pd (OH) 2 and Pt / PtO.
両電極を設けた両端部を接近させてバイメタル形状と
し、電気入力によって彎曲させるようにした特許請求の
範囲第1項記載の密閉式メカノケミカル素子。2. A central part of a mechanochemical element is bent,
The sealed mechanochemical element according to claim 1, wherein both ends provided with both electrodes are brought close to each other to have a bimetal shape and are bent by an electric input.
部の左右の移動を力源として利用する特許請求の範囲第
1項記載の密閉式メカノケミカル素子。3. The sealed mechanochemical element according to claim 1, wherein both ends of the mechanochemical element are fixed, and the lateral movement of the central portion is used as a force source.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25537085A JPH0686864B2 (en) | 1985-11-14 | 1985-11-14 | Sealed mechanochemical element |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP25537085A JPH0686864B2 (en) | 1985-11-14 | 1985-11-14 | Sealed mechanochemical element |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62113870A JPS62113870A (en) | 1987-05-25 |
| JPH0686864B2 true JPH0686864B2 (en) | 1994-11-02 |
Family
ID=17277824
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP25537085A Expired - Fee Related JPH0686864B2 (en) | 1985-11-14 | 1985-11-14 | Sealed mechanochemical element |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0686864B2 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5817782B2 (en) | 2012-06-13 | 2015-11-18 | 株式会社豊田中央研究所 | Hydrogen production catalyst, hydrogen production method and hydrogen production apparatus using the same |
-
1985
- 1985-11-14 JP JP25537085A patent/JPH0686864B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5817782B2 (en) | 2012-06-13 | 2015-11-18 | 株式会社豊田中央研究所 | Hydrogen production catalyst, hydrogen production method and hydrogen production apparatus using the same |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62113870A (en) | 1987-05-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |