JPH03140487A - Electrochemical reactor - Google Patents

Electrochemical reactor

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Publication number
JPH03140487A
JPH03140487A JP1279235A JP27923589A JPH03140487A JP H03140487 A JPH03140487 A JP H03140487A JP 1279235 A JP1279235 A JP 1279235A JP 27923589 A JP27923589 A JP 27923589A JP H03140487 A JPH03140487 A JP H03140487A
Authority
JP
Japan
Prior art keywords
electrode
generation chamber
ozone
product
solid electrolyte
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
Application number
JP1279235A
Other languages
Japanese (ja)
Inventor
Shiro Yamauchi
四郎 山内
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.)
Mitsubishi Electric Corp
Original Assignee
Mitsubishi Electric Corp
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 Mitsubishi Electric Corp filed Critical Mitsubishi Electric Corp
Priority to JP1279235A priority Critical patent/JPH03140487A/en
Publication of JPH03140487A publication Critical patent/JPH03140487A/en
Pending legal-status Critical Current

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  • Oxygen, Ozone, And Oxides In General (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)

Abstract

PURPOSE:To inhibit a side reaction and to efficiently produce the aimed substance by electrolyzing a prescribed raw material to produce the aimed reaction product and also recovering a by-product as electric energy without taking out this by-product to the outside. CONSTITUTION:For example, when water is utilized and ozone is generated, a first electrode 2 is made to a positive pole and a second electrode 4 is made to a negative pole. Water is supplied into a production chamber 8 and electrolyzed. Gaseous O2 contg. ozone is produced and taken out from a discharge port 15 together with unreactive water. Hydrogen ion by-produced at this time is transferred to the second electrode 4 via a solid electrolyte 3 and changed into H2 on the second electrode 4 in a production chamber 9. This H2 is rechanged into hydrogen ion on a third electrode 5. Hydrogen ion is transferred toward a fourth electrode 7 via a solid electrolyte 6 and allowed to react with oxygen (or air) supplied from a feed port 18 on the fourth electrode 7 in a production chamber 10. The produced water is taken out from a discharge port 17. Electric energy generated at this time is conducted to the load 14 and effectively consumed. Thereby ozone is effectively produced without taking out a by-product to the outside of the system.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 この発明は電気化学的な酸化・還元反応を利用して物質
の生、成、精製、分離、濃縮または除去を行う電気化学
反応器に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to an electrochemical reactor that generates, synthesizes, purifies, separates, concentrates, or removes substances using electrochemical oxidation/reduction reactions.

〔従来の技術〕[Conventional technology]

従来、電気化学的な酸化・還元反応を利用して物質の生
成、精製、分離、濃縮、除去等を行う反応器として、e
R素発生器(特公昭51−45557号)、オゾン発生
器(S、 5tucki、 G、 Theis、 R。
Conventionally, e-
R element generator (Special Publication No. 51-45557), ozone generator (S, 5tucki, G, Theis, R.

Kotz、H,Davan電極y、 and H,J、
 Christen、 J。
Kotz, H, Davan electrode y, and H, J.
Christen, J.

1i:lectrochem、 Sac、 : Ili
:IJCTROCHgMICALSCIENCN AN
D TgCHNOLOGY、Februar71985
、第367頁)、 水分除去器(特開昭62−2771
26号)等が挙げられる。
1i: electrochem, Sac, : Ili
:IJCTROCHgMICALSCIENCN AN
D TgCHNOLOGY, February 71985
, p. 367), Moisture Remover (JP-A-62-2771)
No. 26), etc.

上記の反応器はイオン交換膜または固体電解質の両面に
電極を被着し、両a極間に直流電圧を印加することによ
り、原料物質を一万のtll界面でイオン化し、他方の
電極界面で再び分子の状態にする。この結果、物質の生
成、精製、分離、濃縮、除去等が行われる。分離膜とし
てイオン交換gまたは固体電解質を使用しているので、
省スペース、小形化が可能である。さらに反応の種類、
速Rを印加電圧の大きさで制御できるので、効率よく目
的物質を得ることができる。
The above reactor has electrodes attached to both sides of an ion exchange membrane or solid electrolyte, and by applying a DC voltage between both electrodes, the raw material is ionized at the 10,000 tll interface, and at the other electrode interface. Return to molecular state. As a result, substances are generated, purified, separated, concentrated, removed, etc. Since ion exchange or solid electrolyte is used as the separation membrane,
Space saving and miniaturization are possible. Furthermore, the type of reaction,
Since the speed R can be controlled by the magnitude of the applied voltage, the target substance can be obtained efficiently.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

従来の電気化学反応器は目的物質が還元生成物か、酸化
生成物のどちらかである場合が多い。その場合、目的物
質以外の物質が副反応生成物として生成される。例えば
、オゾンを得る場合は目的物質のオゾンは陽極で生成し
、@極では水素又は水を生成する。水素は酸素と反応し
て水を生成する際、爆発的に反応が進行するおそれがあ
り、未処理で放出するには間層があった。
In conventional electrochemical reactors, the target substance is often either a reduction product or an oxidation product. In that case, substances other than the target substance are produced as side reaction products. For example, when obtaining ozone, the target substance ozone is generated at the anode, and hydrogen or water is generated at the @ electrode. When hydrogen reacts with oxygen to produce water, there is a risk that the reaction will proceed explosively, and there is a gap in the process before it can be released untreated.

この発明は上記のような問題点を解決するためになされ
たもので、好ましくない副反応を抑制し、かつ目的物質
が効率よく得られる電気化学反応器を提供することを目
的とする。
This invention was made to solve the above-mentioned problems, and aims to provide an electrochemical reactor that can suppress undesirable side reactions and efficiently obtain a target substance.

〔課題を解決するための手段〕[Means to solve the problem]

第1の発明に係る電気化学反応器は第1の固体電解質を
介して第1(D電極と第2の電極とを配置した第1のセ
ルと、第1の[極が正極に第2の電極が負極になるよう
に接続された電源と、第2の固体電解質を介して第3の
電圧と第4の電極とを配置した第2のセルと、第3の電
圧と第4の電圧との間に接続された負荷と、第1の電圧
が収容された第1の生成室と、第2の電極と第3のa極
とが収容された第2の生成室と、第4の電極が収容され
た第3の生成室を備え念ものである。
The electrochemical reactor according to the first invention includes a first cell in which a first (D) electrode and a second electrode are arranged via a first solid electrolyte, and a first cell in which a first (D) electrode and a second A power source connected so that the electrode becomes a negative electrode, a second cell in which a third voltage and a fourth electrode are arranged via a second solid electrolyte, and a third voltage and a fourth voltage. a load connected between them, a first generation chamber that accommodates the first voltage, a second generation chamber that accommodates the second electrode and the third a-pole, and a fourth electrode. A third generation chamber containing the

第2の発明に係る電気化学反応器は、第1の固体電解質
を介して第1の電極と第2の電極とを配置した第1のセ
ルと、第1の電極が負極に第2の電圧が正極になるよう
に接続された電源と、第2の固体電解質を介して第3の
電圧と第4の電極とを配置した第2のセルと、第3の電
極と第4の電極との間に接続され友負荷と、第1の電極
が収容された第1の生成室と、第2のgLFMと第3の
電極とが収容された第2の生成室と、第4の電極が収容
された第3の生成室とを備えたものである。
The electrochemical reactor according to the second invention includes a first cell in which a first electrode and a second electrode are arranged via a first solid electrolyte, and a second voltage applied to the negative electrode of the first electrode. a second cell in which a third voltage and a fourth electrode are arranged via a second solid electrolyte; a third electrode and a fourth electrode; A first generation chamber connected between and housing a load and a first electrode, a second generation chamber housing a second gLFM and a third electrode, and a fourth generation chamber housing a second gLFM and a third electrode. and a third generation chamber.

〔作用〕[Effect]

この発明においては、生成、精製、分離、濃縮、除去等
が次のように行われる。
In this invention, production, purification, separation, concentration, removal, etc. are performed as follows.

生成においては、第1の電極を正極に、第2の電極を負
極にし、第1の生成室に水が供給されると、次の反応が
行われる。即ち、第1のく極面上で、3H20→6H+
−+−Hog + 6e  、 3H2046H++i
−Q、+56− により第1の生成室にオゾンを含有し
た酸素ガスが生成される。
During generation, the first electrode is used as a positive electrode, the second electrode is used as a negative electrode, and when water is supplied to the first generation chamber, the following reaction takes place. That is, on the first pole surface, 3H20→6H+
-+-Hog + 6e, 3H2046H++i
-Q, +56- generates oxygen gas containing ozone in the first generation chamber.

精製1分#1.濃縮においては、第1の電極を正画に、
第2の[極を負極にし、第1の生成室にH2+H,0−
)−0□+N2  が供給されると5次の反応が行われ
る0即ち、第2の電極面上にH2ガスが発生し、第1の
生成室に供給された原料からH2ガスがpII製、分離
、濃縮される。
Purification 1 minute #1. In concentration, the first electrode is used as a positive image,
The second [electrode is made negative, and H2+H, 0-
) -0 Separated and concentrated.

除去においては、上記精製、分離、濃縮の場合と同じ設
定の下で2次の反応が行われる。即ち、第2の生成室に
発生したH2ガスは第2のセルの第3の[極上で水素イ
オンとなって第4の電極へ向って移動し、第3の生成室
の酸素と反応して水となって排出される。
In the removal, a secondary reaction is performed under the same settings as in the purification, separation, and concentration described above. That is, the H2 gas generated in the second generation chamber becomes hydrogen ions at the third electrode of the second cell, moves toward the fourth electrode, and reacts with oxygen in the third generation chamber. It is discharged as water.

還元においては、第1の成極を負極に、第2の11jF
Mを正極にして、原料として第1の生成室にベンゾキノ
ンを供給し、負荷のスイッチ■をオフにした状態で第2
の生成室にH2ガスを供給しfc場合、次の反応が行わ
れる。
In the reduction, the first polarization is made negative and the second 11jF
With M as the positive electrode, benzoquinone is supplied as a raw material to the first generation chamber, and with the load switch
When H2 gas is supplied to the generation chamber fc, the following reaction takes place.

(1)第2の電極から「イオンが第1のaFMに移動す
る。(2)第1の電極上でベンゾヒドロキノンが還元作
用によシ生成される。(3)反応終了後、負荷のスイッ
チ(至)をオンにして第2生成室の未反応のH2ガスは
第3の電極から計イオンとなって第4の電極へ移動し、
第3の生成室でH2O(水)となって排出される。
(1) Ions move from the second electrode to the first aFM. (2) Benzohydroquinone is produced by reduction on the first electrode. (3) After the reaction is completed, the load is switched. (to) is turned on, the unreacted H2 gas in the second generation chamber becomes total ions from the third electrode and moves to the fourth electrode.
It becomes H2O (water) in the third generation chamber and is discharged.

還元の例として、上記の他に第1の生成室にマレイン酸
を原料として供給し念場合、第1の電極上でコハク酸が
生成される。
As an example of reduction, if maleic acid is supplied as a raw material to the first production chamber in addition to the above, succinic acid is produced on the first electrode.

〔実施例〕〔Example〕

以下、この発明の実施例を図について説明する。 Embodiments of the present invention will be described below with reference to the drawings.

実施例(1)「オゾン発生」第1図はこの発明の一実施
例であるオゾン発生用電気化学反応器の構成図である。
Example (1) "Ozone Generation" FIG. 1 is a block diagram of an electrochemical reactor for ozone generation which is an embodiment of the present invention.

図において、(1)は反応容器、(2)は第1の電(至
)で、チタンメツシュにβ二酸化鉛が電着されているも
のである。(3)は第1の固体電解質で、水素イオ7 
J [性のデュポン社製Nafionl17 (商品名
)である。(4)は第2の電極で、膨張化黒鉛が使用さ
れている。(5)は第3の電極で、無電解メツキで成膜
され之多孔性の白金メツキ層である。
In the figure, (1) is a reaction vessel, and (2) is a first electrode, in which β-lead dioxide is electrodeposited on a titanium mesh. (3) is the first solid electrolyte, hydrogen ion 7
J [Nafionl17 (trade name) manufactured by DuPont. (4) is the second electrode, and expanded graphite is used. (5) is the third electrode, which is a porous platinum plating layer formed by electroless plating.

(6)は第2の固体電解質でNafionl17である
。(7)は第4の[極で無電解メツキで成膜された多孔
性の白金メツキ層である。(8)は第1の生成室%(9
)は第2の生成室、(IGは第3の生成室、aυは仕切
板で、絶縁性の材料でできている。O諺は制御器で、後
述の電源α枠の電圧を制御して画電極+2) 、 (4
)に印加する。(至)は電源で、第tO1E極(2)が
陽極、第2の電極(4)が陰極になるよりに直流電圧2
〜5vを印加するものである。α4は負荷である。α谷
は第1の生成物排出口、(至)は第1の原料供給口で、
原料として水が供給される。靭は第3生成物排出口、ω
は第2の原料供給口で、空気ま九は酸素が供給される。
(6) is the second solid electrolyte, which is Nafionl17. (7) is a porous platinum plating layer formed by electroless plating at the fourth electrode. (8) is the first generation chamber% (9
) is the second generation chamber, (IG is the third generation chamber, aυ is the partition plate, which is made of insulating material. The proverb is a controller, which controls the voltage of the power supply α frame, which will be described later. Image electrode +2), (4
). (to) is the power supply, and the tO1E electrode (2) is the anode and the second electrode (4) is the cathode, so the DC voltage is 2.
~5v is applied. α4 is a load. α valley is the first product discharge port, (to) is the first raw material supply port,
Water is supplied as a raw material. Toughness is the third product outlet, ω
is the second raw material supply port, and oxygen is supplied to the air port.

0gは第2の生成物排出口、jは切換バルブ、0、c!
2はリード線である。なお、第1の電極(2)と第1の
固体電解質(3)と第2の電極(4)とで第1のセルの
を構成し、第3の電極(5)と第2の固体電解質(6)
と第4の電極(力とで第2のセル□□□を構成している
0 次に動作について説明する。第1の原料供給口(至)か
ら原料としての水が第1の生成室(8)内へ供給される
。水は第1の電極界面上で(11式および(2)式の反
応が起こる。
0g is the second product outlet, j is the switching valve, 0, c!
2 is a lead wire. Note that the first electrode (2), the first solid electrolyte (3), and the second electrode (4) constitute the first cell, and the third electrode (5) and the second solid electrolyte constitute the first cell. (6)
The second cell □□□ is made up of the fourth electrode and the fourth electrode. 8) The reactions of equations (11 and (2)) occur on the first electrode interface.

3H20→6H””−OB + 6 e−−−−−(1
)3 H20→6 H“+ 10 t ” 6 e −
・= =・===  !21第1の生成室(8)で、オ
ゾンを含有した酸素ガスが生成され、未反応の水ととも
に第1の生成物排出口(至)から系外にと9出される。
3H20→6H""-OB + 6 e------(1
)3 H20→6 H“+10 t” 6 e −
・= =・=== ! 21 In the first generation chamber (8), oxygen gas containing ozone is generated and discharged from the system through the first product outlet (9) together with unreacted water.

−万、分解され几水素イオンは第1の固体電解質(3)
の中を第2の電極(4)へ向って移動し、第2の生成室
(9)内の第2の11電極(4)上で次の反応が起こる
- 10,000, the decomposed hydrogen ions are the first solid electrolyte (3)
The next reaction occurs on the second 11 electrode (4) in the second production chamber (9).

6 H+= 6 e −→3t(2=====−曲(3
)生成した水素は第3の電極(5)上で再び水素イオン
となり、第4の電極(力へ向って移動し、第3の生成室
C10内の第4の電極(力士で、第2の原料供給口部か
ら供給される酸素(又は空気中の酸素)によって次の反
応が起こる。
6 H+= 6 e −→3t(2=====−song(3
) The generated hydrogen becomes hydrogen ions again on the third electrode (5), moves toward the fourth electrode (force), and moves toward the fourth electrode (in the sumo wrestler, the second The following reaction occurs due to oxygen (or oxygen in the air) supplied from the raw material supply port.

6H+−t−702+ 6e−+ 3H20−・−=−
・(4)生成した水は第3の生成室al内に蓄積される
が、やがて第3の生成物排出口αηから系外に排出され
る0 発生したオゾンを第3の生成UaOに原料として送り込
むことによって% H,O(水)として処理できるので
、余剰のオゾンを処理して系外に排出できる0 この過程で、第1のセルのでは外から電気エネルギーを
与えて電気分解により目的生成物(オゾンを含有し7t
[素ガス)を得る。第2のセル例では副反応生成物(H
2)と空気(0□)を原料にして、燃料電池の原理で外
部に電気エネルギーを取シ出し、適当な負荷に通電する
ことにより、有効に消費することができる。
6H+-t-702+ 6e-+ 3H20-・-=-
・(4) The generated water is accumulated in the third generation chamber al, but is eventually discharged to the outside of the system from the third product outlet αη.The generated ozone is used as a raw material for the third generated UaO. By supplying ozone, it can be treated as % H, O (water), so excess ozone can be treated and discharged from the system. During this process, electrical energy is applied from outside to the first cell to produce the desired product through electrolysis. (contains ozone, 7 tons)
Obtain [elementary gas]. In the second cell example, the side reaction product (H
Using 2) and air (0□) as raw materials, electrical energy can be extracted externally using the principle of a fuel cell and can be effectively consumed by supplying electricity to an appropriate load.

上記、実施例では目的生成物がオゾンであるために、第
1の電極(2)の材質として、耐酸化性の強いβ二酸化
鉛を使用した。しかし、酸素を目的生成物とする場合、
第1のit 11(2)の材質としてβ二酸化鉛の代シ
に多孔性の白金メツキ層を用いることによシ、第1の生
成室でのオゾンの生成はなく、酸素のみ生成する。そし
て、第2の生成室(9)および第3生成室σ〔での反応
はオゾンの場合と同じである。
In the above examples, since the target product was ozone, beta lead dioxide, which has strong oxidation resistance, was used as the material for the first electrode (2). However, when oxygen is the target product,
By using a porous platinum plating layer instead of β lead dioxide as the material of the first IT 11(2), no ozone is generated in the first generation chamber, and only oxygen is generated. The reactions in the second generation chamber (9) and the third generation chamber σ are the same as in the case of ozone.

上記、実施例では第1の11E極(2)2よび第3の電
極(5)が陽極、第2のに極(4)および第4の電極(
7)が陰極で、第1の生成室(8)の原料が酸化分解さ
れる例を示したが、極性を逆にして第1の電極(2)お
よび第3のa極(5)が陰極、第2のa極(4)および
第4の電極(力が陽極で、第1の生成室(8)の原料を
還元分解して目的物質を得ることも可能である。例えば
、有機電解の場合は原料として、 RCH=CHR’と
いう二重結合を有する物質で、目的物質がRCH2CH
!a’である場合の例について述べる。各電極上では次
の反応が起こる。
In the above example, the first 11E electrode (2) and the third electrode (5) are the anode, and the second electrode (4) and the fourth electrode (
7) is the cathode, and the raw material in the first generation chamber (8) is oxidized and decomposed. , the second a-electrode (4) and the fourth electrode (the power is the anode), and it is also possible to reductively decompose the raw material in the first generation chamber (8) to obtain the target substance. For example, in organic electrolysis In this case, the raw material is a substance with a double bond RCH=CHR', and the target substance is RCH2CH
! An example where a' is the case will be described. The following reactions occur on each electrode.

先ず、スイッチ(支)をオフにした状態で、第1のIE
ffi12)上では RCH=CHR’ +2H++2e −→RCH2CH
2R’・・・・・・・・・・・・・・・ (5)第2の
電極(4)上では、(6)式の反応が生ずる。
First, with the switch (support) turned off, turn on the first IE
ffi12) on RCH=CHR' +2H++2e -→RCH2CH
2R' (5) On the second electrode (4), the reaction of formula (6) occurs.

H2→2H++2e−13,21911890810,
(6)次に、スイッチ(至)をオンにすると、第3の電
極(5)上では H2→2H” + 2e−・・・・・・・・・・・・・
・・  (7)第4の11L極(7)上では 2H++102+2e−→H20・・・・・・・・・・
・・・・・ (8)となる。
H2 → 2H++2e-13, 21911890810,
(6) Next, when the switch (to) is turned on, on the third electrode (5) H2 → 2H" + 2e-...
... (7) On the fourth 11L pole (7), 2H++102+2e-→H20...
...(8).

このようにして、目的生成物RCH2CH,R’が得ら
れ、その生成過程で生ずる水素は系外に出ることなく安
全である。
In this way, the desired product RCH2CH,R' is obtained, and the hydrogen generated during the production process is safe without leaving the system.

実施例+23rベンゾヒドロキノンの発生」第2図は他
の実施例を示す構成図である。図において、第1の電極
(2)を電源03の負極に、第2の電極(4)を正極に
接続して、スイッチ(至)をオフにしてパルプ囚を開に
して第1の生成室(8)に原料としてベンゾキノンを供
給する。さらに、第2の生成室(9)にバルブ■を通し
てH2ガスを供給する。この場合、次の反応が行われる
Example +2 Generation of 3r benzohydroquinone" FIG. 2 is a block diagram showing another example. In the figure, the first electrode (2) is connected to the negative electrode of the power source 03, the second electrode (4) is connected to the positive electrode, the switch (to) is turned off, the pulp container is opened, and the first production chamber is opened. (8) Supply benzoquinone as a raw material. Furthermore, H2 gas is supplied to the second generation chamber (9) through valve (2). In this case, the following reaction takes place.

■計イオンが第20a極(4)から第1の電極(2)へ
移動する。■第1oii電極(2)上でベンゾヒドロキ
ノンが還元作用によシ生成される。■第2の生成室(9
)の未反応のH2ガスは、スイッチ(至)をオンにする
ことによシ第3の電極(5)からH+イオンとなって第
4の電極(カへ移動し、第3の生成室α1で02と反応
してH2Oで排出される。
■Measure ions move from the 20a-th electrode (4) to the first electrode (2). (2) Benzohydroquinone is produced on the first oii electrode (2) by a reductive action. ■Second generation chamber (9
), the unreacted H2 gas becomes H+ ions from the third electrode (5) and moves to the fourth electrode (F) by turning on the switch (to), and is transferred to the third generation chamber α1. It reacts with 02 and is discharged as H2O.

上記において、第1の生成室(8)のガスをポンプ(至
)を介して循環させることによって濃縮し、最終的にパ
ルプ(至)から高m度のベンゾヒドロキノンを抽出でき
る。
In the above, the gas in the first production chamber (8) can be concentrated by circulating it through a pump, and finally high-molecular-weight benzohydroquinone can be extracted from the pulp.

還元反応の他の例として、第1の生成室(8)にマンイ
ン酸を原料として供給した場合、第1の電極(2)でコ
ハク酸が生成される。
As another example of the reduction reaction, when manic acid is supplied as a raw material to the first production chamber (8), succinic acid is produced at the first electrode (2).

上記実施例において、固体電解質+31 、 (6)を
酸素イオン![性向体等の各種21!電性固体としても
同様の効果が期待できる。
In the above example, the solid electrolyte +31, (6) is oxygen ion! [Various types of propensity bodies, etc. 21! A similar effect can be expected as an electrically conductive solid.

〔発明の効果〕〔Effect of the invention〕

以上のように、第1の発明によれば第1の電極を正極に
し、第2のa極を負極にして第1の生成室に第1の原料
を供給することによって、目的とする反応生成物に副生
ずる副生成物が系外に出ることなく処理されて排出され
るので、副生成物が有害物質であっても安全性が維持で
きる。また、副生成物と第2の原料との反応で電気エネ
ルギーとしても回収できる。
As described above, according to the first invention, by supplying the first raw material to the first production chamber with the first electrode as the positive electrode and the second a-electrode as the negative electrode, the desired reaction can be produced. Since the by-products produced by the product are treated and discharged without leaving the system, safety can be maintained even if the by-products are harmful substances. Furthermore, it can be recovered as electrical energy through the reaction between the by-product and the second raw material.

第2の発明によれば、第1の電極を負極にし、第2の電
極を正極にすることによって、酸化生成物および還元生
成物の目的物質が得られる。
According to the second invention, target substances of oxidation products and reduction products can be obtained by using the first electrode as a negative electrode and the second electrode as a positive electrode.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はこの発明の一実施例を示す電気化学反応器の構
成図、第2図は他の実施例を示す構成図である。 図において、(2)は第1のt電極%(3)は第1の固
体電解質、(4)は第2の電極、(5)は第3の電極、
(6)は第2の固体電解質、(力は第3の電極、(8)
は第1の生成’!、(9)は第2の生成室、uIは第3
の生成室、(至)は電源、(14は負荷、のは第1のセ
ル、囚は第2のセルである0■はスイッチである0 なお、図中、同一符号は同一、又は相当部分を示す。
FIG. 1 is a block diagram of an electrochemical reactor showing one embodiment of the present invention, and FIG. 2 is a block diagram showing another embodiment. In the figure, (2) is the first t electrode, (3) is the first solid electrolyte, (4) is the second electrode, (5) is the third electrode,
(6) is the second solid electrolyte, (force is the third electrode, (8)
is the first generation'! , (9) is the second generation chamber, uI is the third
The generation chamber is, (to) is the power supply, (14 is the load, 1 is the first cell, 2 is the second cell, 0■ is the switch, shows.

Claims (2)

【特許請求の範囲】[Claims] (1)第1の固定電解質を介して第1の電極と第2の電
極とを配置した第1のセル、上記第1の電極が正極に上
記第2の電極が負極になるように接続された電源、第2
の固体電解質を介して第3の電極と第4の電極とを配置
した第2のセル、上記第3の電極と上記第4の電極との
間に接続された負荷、上記第1の電極が収容された第1
の生成室、上記第2の電極と上記第3の電極とが収容さ
れた第2の生成室、上記第4の電極が収容された第3の
生成室を備えた電気化学反応器。
(1) A first cell in which a first electrode and a second electrode are arranged via a first fixed electrolyte, and the first electrode is connected to the positive electrode and the second electrode is the negative electrode. power supply, 2nd
a second cell in which a third electrode and a fourth electrode are arranged via a solid electrolyte; a load connected between the third electrode and the fourth electrode; First housed
An electrochemical reactor comprising: a generation chamber, a second generation chamber housing the second electrode and the third electrode, and a third generation chamber housing the fourth electrode.
(2)第1の固体電解質を介して第1の電極と第2の電
極とを配置した第1のセル、上記第1の電極が負極に上
記第2の電極が正極になるように接続された電源、第2
の固体電解質を介して第3の電極と第4の電極とを配置
した第2のセル、上記第3の電極と上記第4の電極との
間に接続された負荷、上記第1の電極が収容された第1
の生成室、上記第2の電極と上記第3の電極とが収容さ
れた第2の生成室、上記第4の電極が収容された第3の
生成室を備えた電気化学反応器。
(2) A first cell in which a first electrode and a second electrode are arranged via a first solid electrolyte, the first electrode being connected as a negative electrode and the second electrode as a positive electrode. power supply, 2nd
a second cell in which a third electrode and a fourth electrode are arranged via a solid electrolyte; a load connected between the third electrode and the fourth electrode; First housed
An electrochemical reactor comprising: a generation chamber, a second generation chamber housing the second electrode and the third electrode, and a third generation chamber housing the fourth electrode.
JP1279235A 1989-10-25 1989-10-25 Electrochemical reactor Pending JPH03140487A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1279235A JPH03140487A (en) 1989-10-25 1989-10-25 Electrochemical reactor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1279235A JPH03140487A (en) 1989-10-25 1989-10-25 Electrochemical reactor

Publications (1)

Publication Number Publication Date
JPH03140487A true JPH03140487A (en) 1991-06-14

Family

ID=17608321

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1279235A Pending JPH03140487A (en) 1989-10-25 1989-10-25 Electrochemical reactor

Country Status (1)

Country Link
JP (1) JPH03140487A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6692617B1 (en) * 1997-05-08 2004-02-17 Applied Materials, Inc. Sustained self-sputtering reactor having an increased density plasma
US7416979B2 (en) 2001-07-25 2008-08-26 Applied Materials, Inc. Deposition methods for barrier and tungsten materials
US9051641B2 (en) 2001-07-25 2015-06-09 Applied Materials, Inc. Cobalt deposition on barrier surfaces
EP2886681A1 (en) * 2013-12-20 2015-06-24 Forschungszentrum Jülich GmbH Electrochemical electrolytic cell for the electrolysis of water and method for operating the same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6692617B1 (en) * 1997-05-08 2004-02-17 Applied Materials, Inc. Sustained self-sputtering reactor having an increased density plasma
US7416979B2 (en) 2001-07-25 2008-08-26 Applied Materials, Inc. Deposition methods for barrier and tungsten materials
US9051641B2 (en) 2001-07-25 2015-06-09 Applied Materials, Inc. Cobalt deposition on barrier surfaces
US9209074B2 (en) 2001-07-25 2015-12-08 Applied Materials, Inc. Cobalt deposition on barrier surfaces
EP2886681A1 (en) * 2013-12-20 2015-06-24 Forschungszentrum Jülich GmbH Electrochemical electrolytic cell for the electrolysis of water and method for operating the same

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