JPS5917144A - Galvanic cell type oxygen concentration meter - Google Patents

Galvanic cell type oxygen concentration meter

Info

Publication number
JPS5917144A
JPS5917144A JP57127896A JP12789682A JPS5917144A JP S5917144 A JPS5917144 A JP S5917144A JP 57127896 A JP57127896 A JP 57127896A JP 12789682 A JP12789682 A JP 12789682A JP S5917144 A JPS5917144 A JP S5917144A
Authority
JP
Japan
Prior art keywords
lead
oxygen
electrolyte
organic acid
diaphragm
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.)
Granted
Application number
JP57127896A
Other languages
Japanese (ja)
Other versions
JPH032258B2 (en
Inventor
Hisashi Kudo
工藤 寿士
Yuko Fujita
藤田 雄耕
Ikuo Tanigawa
谷川 郁夫
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.)
Japan Storage Battery Co Ltd
Nihon Denchi KK
Original Assignee
Japan Storage Battery Co Ltd
Nihon Denchi KK
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 Japan Storage Battery Co Ltd, Nihon Denchi KK filed Critical Japan Storage Battery Co Ltd
Priority to JP57127896A priority Critical patent/JPS5917144A/en
Publication of JPS5917144A publication Critical patent/JPS5917144A/en
Publication of JPH032258B2 publication Critical patent/JPH032258B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/403Cells and electrode assemblies
    • G01N27/404Cells with anode, cathode and cell electrolyte on the same side of a permeable membrane which separates them from the sample fluid, e.g. Clark-type oxygen sensors

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Secondary Cells (AREA)

Abstract

PURPOSE:To obtain an oxygen concn. meter having along service lefe by using a metal (oxide) capable of reducing oxygen highly actively as a positive pole and lead as a negative pole of lead and using a mixture of propionic acid and alkali metallic salt or NH4 salt of an organic acid and lead compound as an electrolyte. CONSTITUTION:The positive pole 1 is a Pt plate, etc. capable of reducing oxygen highly actively, the negative pole 2 is lead, the electrolyte 3 is the mixed solution of the organic acid such as propionic acid and organic acid alkali metallic salt such as potassium propionate or NH4 salt and lead oxide. A diaphragm 4 consisting of copolymer of F2C=CF2 and H2C=CH2 is fixed to a holder 6 made of PVC resin by an O-ring 5. By measuring both end voltages of a resistance 7 between the poles 1 and 2, O2 amount transmitting through the diaphragm 4 is measured to measure O2 concn. in outer atmosphere of the diaphragm or in the solution. Thereby, H2 is not generated, precipitation of lead carbonate due to CO2 in the detecting gas is prevented, the solubility of the lead oxide is increased, and the service life is prolonged remarkably than that of conventional oxygen concn. meter using alkali electrolyte.

Description

【発明の詳細な説明】 本発明はガルバニ7にl(1式酸素濃度81の改曳に係
l)、その目的とするところは、検知気体中に含まれる
炭酸カスの影響を受けず、かつスト命の長い酸素p l
’l:計を捏111:ぜんとするにある。
DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to a galvanic device 7 (related to the modification of type 1 oxygen concentration 81), and its purpose is to be unaffected by carbon dioxide scum contained in the detected gas, and Long-life oxygen p l
'l: Calculate the total 111: It's completely there.

カルバニ゛11(北式酸素711度叶は、一般に手軽で
安fil+であI)、かっIf’; faで作動するの
で、広い分野で7−11用さfLでおり、酸素の電気f
b学的1元に有効な金11べからf(ろ+E bfJ(
と鉛からなる負l111+とIW;す・r改とからf(
ろ′山二池で+/41戊木]1、iE l「Jことtg
、 li虫との間1こ一疋の抵抗を接続し1ことき、そ
こに流ねる1−■流と酸素濃1¥との間に)q練性があ
ることを利用している。
Calvany 11 (northern type oxygen 711 degree cylinder is generally easy and cheap fil + I), kaIf';fa, so it is used in a wide range of fields.
Gold 11be to f(ro+E bfJ(
and the negative l111+ made of lead and IW;s・r modified and f(
Ro'yama Niike de+/41 Bogi] 1, iE l "J tg
, It takes advantage of the fact that there is a q-resistance between the 1-■ flow flowing there and the oxygen concentration 1 yen by connecting a resistance of 1 sq.

従来のガルバニ゛Ii曲式?素濃度計には2つの欠点が
ある。l一つはセンサの寿命が6ケ月〜10ケ月と非常
に短かいfコめ、1年の円1〜2回は必ずセンサ部を新
しいものと交換しなければなら4cいこと。
Conventional galvanic Ii curve? There are two drawbacks to densitometers. One is that the sensor has a very short lifespan of 6 to 10 months, and the sensor must be replaced with a new one once or twice a year.

他の1つは、比1咬的高傾度の炭酸ガスを含む検知気体
中では閏用出米ないあるいは自端に/liなが短かくな
ることでJ〕る。
The other reason is that in a detection gas containing carbon dioxide gas with a relatively high gradient, there is no jump or the /li becomes short.

これらは電解液として、水酸1じカリウムあるいは水酸
1bナトリウムの水溶液が用いられていることに由来す
る。
This is due to the fact that an aqueous solution of 1b potassium hydroxide or 1b sodium hydroxide is used as the electrolyte.

以下、この点について説明才ろ。Please explain this point below.

ガルバニ電曲式酸素濃度言1にはアルカリ電解液を用い
jこ場合、IE−では、 02 + 2H,20+4e  −+  40)l  
   −(11なる反応が起り、負嘩では 2ρ1=1−4(刀”−−29bO+ 2LL+0−1
40m 0.  (2]なる反応が、r4ろ。負廟1フ
応生成物でJ)ろ9 b Uは1)(解輝中に(i;解
して、沿廟の&而は、INにりf新さ第1る。ところか
、′11j解液が1同反応14:、 W、物で飽和され
ろと、色画大面は不fIIIIII序化さば]、負16
ハの過電圧が1(9大するrコめに、市祷と負囁との間
に流れる屯mlか変化し、酸素4度と電mlとの一定の
1v4係が崩オ]、峻素噛度計の葎6aが1尽きろ。
In this case, in IE-, 02 + 2H, 20+4e −+ 40) l
-(11 reactions occur, and in a fight 2ρ1=1-4(sword"--29bO+ 2LL+0-1
40m 0. (2) The reaction becomes r4 . Negative temple 1 reaction product J) 9 b U is 1) Newness is the first thing. However, '11j solution is 1 same reaction 14:, W, the large color screen is saturated with things, negative 16
The overvoltage of Ha is 1 (9 times the ML that flows between the city prayer and the negative whisper changes, and the constant 1v4 relationship between oxygen 4 and electric ml collapses), The meter runs out of 6a.

従来、アルカリ醒1’li液を用いrこガルlく二Y[
II+、式酸I濃興計の寿命か′禮かかつ1このは、@
両生酸物であるPbUのアルカリ水jb液に討゛4−る
溶解IWか1こかtでか0.1モル/ 5 tIij 
IQ:と小さかつfこからに他lcら4.Cい。
Conventionally, an alkaline aqueous solution was used to prepare the liquid.
II+, is the lifespan of the formula acid I concentration meter? 1 This is @
PbU, an amphibiotic acid, is dissolved in alkaline water at a concentration of 0.1 mol/5 t per ton of IW.
IQ: small and f 4. C.

−り、検知気体中に比I咬的多喰の炭酸ガスが含まオ]
ているときには、負1他では+’+il Kの(2)式
のようニPbUが生1戊才る代+1 ニ不iff、性の
炭酸鉛(pl+cUa )あるいは頃哉性炭酸沿(Pb
20すB(OH) 2 )が生成して@商の過電圧が著
しく増大するrコめに、酸素濃度のが11疋ができなく
なる。
-The detected gas contains a relatively large amount of carbon dioxide]
When it is negative 1, +'+il K's equation (2) shows that 2PbU is born 1 year old +1 2iff, and the lead carbonate (pl+cUa) or the lead carbonate (Pb
20B(OH) 2 ) is generated and the overvoltage of the quotient increases significantly, and the oxygen concentration becomes impossible.

不発明は、従来の酸素濃度、4tかもつ上述のuJlき
欠点を除去せA2と才ろものである。
The invention is unique to A2, which eliminates the above-mentioned disadvantage of the conventional oxygen concentration of 4 tons.

長野命でしかも炭酸ガスの影響を受け4〔いガルバニ市
; 1+0式酸素濃1す、計の電解我に必要とさオ]る
条件は、まず反応生成物である酸化鉛の電解it&に討
嘩からの水素発生かないことである。
Nagano Life is affected by carbon dioxide gas, and the conditions necessary for electrolysis of lead oxide, which is a reaction product, are first discussed in the electrolysis of lead oxide, which is a reaction product. There is no hydrogen generation from combustion.

かかる条件を満足するト・・解放として、本輸出頼者等
はプロピlノン酸とアルカリ金用も【7くはアンモニア
の有機酸塩と鉛化合物との混合水溶液を光1−7し1こ
In order to satisfy these conditions, the exporter, etc. may also use a mixed aqueous solution of propylononic acid and alkali gold [7] or a mixed aqueous solution of an organic acid salt of ammonia and a lead compound. .

以下、このt毘合水溶液について説明−する。This aqueous solution will be explained below.

ijルバニ肛池式酸素Z@度計に酸性電解液を用い1こ
場合、 11三IJJIでは、02−1−4H−4−4e  −
+ 2H−20−=・(31負施では、2Pb + 2
J120 →2PbU+4fl +4e  ・・・・(
41なる反応が起こり、負囁ではアルカリ電解液を用い
fコ場合と同様酸化鉛(PbO)が生成する。
In this case, 113 IJJI uses an acidic electrolyte in the Lubanian oxygen Z@meter. In this case, 02-1-4H-4-4e -
+ 2H-20-=・(31 negative addition, 2Pb + 2
J120 →2PbU+4fl +4e...(
A reaction 41 occurs, and lead oxide (PbO) is produced in the same manner as in the case of using an alkaline electrolyte.

酸化鉛のプロピオン酸水に液に対するld解度は、1.
5モル/eであり、アルカリ電解液に対するそれの15
倍である。
The ld solubility of lead oxide in propionic acid water is 1.
5 mol/e and its 15 for alkaline electrolyte
It's double.

換言すれば、プロピオン酸を゛α解欣と才ろガルバニ電
器式酸素Ii滝度計は従来のそfl、の15 倍の寿命
を何才ろ 欠に正l′11μからの水素発生の’f+1頭について
説明する、正%+おの水素発生平衡型(ffは欠の(5
)式で与えらilろ。
In other words, the galvanic oxygen Ii waterfall meter, which uses propionic acid as a solution, has a lifespan 15 times longer than the conventional one. To explain the head, correct % + each hydrogen generation equilibrium type (ff is missing (5
) is given by the formula.

5) ココテ、E H・・−・25°Cにおける水素う6生平
衡?L IffPl−1≧・・・・・・水素の分匝 pkfi、  ・・・・・・電解液のP8つま1.) 
(51民において、Pすが小さくなtl、ばなるほど、
iE tMの水素発生平衡載位が目になり、そit t
ごけ1[[餉から水素が発生し易くなる。プロピオン酸
水浴液のようにpリ が小さい俗液をrli:解放と−
rると、殊に酸素71機+iの低い検知気体の酸素濃1
隻を測定−1ろQ eにはi″E1枳の電イイlがかな
り卑となるので、水素が発生し易< fする。
5) Kokote, E H...Hydrogen bioequilibrium at 25°C? L IffPl-1≧...Hydrogen pkfi, P8 pkfi of electrolyte 1. )
(In the 51st people, P is small, tl is small,
iE tM hydrogen generation equilibrium loading is visible, so it t
Moss 1 [[Hydrogen is easily generated from the moss. A common liquid with a small p such as a propionic acid water bath liquid is called rli: release and -
r, especially if the oxygen concentration of the detected gas is low, especially oxygen 71 + i
Since the electric current of i''E1 is quite base in Qe, hydrogen is likely to be generated.

逆にpHが入きく4〔ればIF画の水素発生率iがr 
7K Blは卑になり、水素が発生しにくくなる。
On the other hand, if the pH increases, the hydrogen generation rate i in the IF picture becomes r
7K Bl becomes base, making it difficult to generate hydrogen.

そこでプロピオンAIP″′2〜3月こアルカリ金1肩
もしくはアンモニアの有機酸塩、例えばプロピオン酸塩
、酢酸塩、シュウ酸塩、錯酸塩、クエン酸塩、などを加
えていくと溶液のpHは犬きくf〔る。
Therefore, by adding organic acid salts of alkali gold or ammonia, such as propionate, acetate, oxalate, complex acid salts, citrate, etc., the pH of the solution increases. The dog is listening.

ここでRHのPh3が7よりも大きくなってアルカリ側
に移行[7てし逢うと炭酸ガスの影響を受けるようにな
るのでP唱は7以F、好牛しくは4〜65に押さするよ
うにすることが肝要である。
At this point, the Ph3 of the RH becomes larger than 7 and shifts to the alkaline side [If it reaches 7, it will be affected by carbon dioxide gas, so the pH should be set to 7F or higher, preferably 4 to 65. It is important to do so.

しか[7溶液のPh5が4〜65の範囲では、まだ水素
発生の危険がある。−万、鉛の平衡電位は/X’式のよ
うに表わさ11、 ””l]/Pb”= −0,1367+0.02961
 o(<(Pb″〕(Vvs SUE )=(61?ニ
ー0でK P +)/P b +l・・・・・・25°
Cにおける鉛の平衡’+5イイ1(PI)  j  ・
・・・・電解液中の鉛イオンの活潰鉛イオンの添加量が
多ければ多いほど3咄の電位、換言すれば正1他の°電
位がより財になることかわかる。即ち、鉛の平衡型4V
が水素イζ生平術′市イー)γよりも財になるまで、上
述の混合rPJM、に鉛イオンを添加してやれば水素は
絶対@生じなくなる。
However, if the Ph5 of the [7 solution is in the range of 4 to 65, there is still a risk of hydrogen generation. -10,000, the equilibrium potential of lead is expressed as /X'11, ""l]/Pb" = -0,1367+0.02961
o(<(Pb″)(Vvs SUE)=(61? K P + at knee 0)/P b +l...25°
Equilibrium of lead at C'+5ii1(PI) j ・
...It can be seen that the greater the amount of active crushed lead ions added to the electrolytic solution, the better the potential of 3 liters, in other words, the potential of positive 1 and other degrees becomes more beneficial. That is, lead balanced 4V
If lead ions are added to the above-mentioned mixture rPJM until hydrogen becomes better than γ, hydrogen will never be produced.

鉛イオンは、例えば酸(? 、G 、プロピオンロ!!
鉛あるいは酢酸塩の叩き鉛化合物の11つでFMS I
JII才11.ばよい。
Lead ions are, for example, acids (?, G, propionro!!
FMS I with lead or acetate beaten lead compound 11
JII Sai 11. Bye.

しかし、その添加量は水素うi生を同1辞゛Cきる最少
あろ峙化沿のr谷解度か減少し、で々品が短力・くりC
る。
However, the amount added decreases as the hydrogen production reaches the minimum level required to reduce hydrogen production at the same time.
Ru.

かくして得らt’trこ泥合電IQ+! ++(、+列
えば2モル/eプロピオン酸と35モル/Cブロビオノ
酸カリと01モル/4酸化1ηとの混合71り、 (e
41PiのP8は6.25 、 コ(J)時の水素−d
生’lI衝’jTt 67は−0,6’ I V (v
S8UE )、yの平衡°「1を位は−1,60V (
vs 8CE )とr、(11、こO)^4合M液中で
は鉛の平衡電位の5か水素発生平衡電イ)γよりもtl
になるので、IE嘩から水素が元生−することは4〔い
。まfこ浴液は酸FI:であるf、二め炭酸ガスQ〕影
響を受けることも4Cい。
In this way, I got IQ+! ++(, + column: 71 mixture of 2 mol/e propionic acid, 35 mol/C potassium brobionate and 01 mol/4 1η oxide, (e
P8 of 41Pi is 6.25, hydrogen-d when co(J)
Raw 'lI opposition'jTt 67 is -0,6' I V (v
S8UE ), y equilibrium ° "1" is -1,60V (
vs 8CE) and r, (11, this O) ^4 In the combined M solution, 5 of the equilibrium potential of lead or hydrogen generation equilibrium electric potential) tl than γ
Therefore, it is impossible for hydrogen to be generated from IE. The bath liquid is also affected by acid FI: f, and carbon dioxide gas Q].

以」二、本発明によるカルバニ市2111式酸素畿1¥
計の゛直解故について述べ1こが、il4に木梵明fP
説明才ろfコめ、以ドー実施例を図面に沿って詳述する
2. Calbani city type 2111 oxygen ki according to the present invention 1 yen
Explaining the reason for the direct solution to the equation, 1.
For the sake of explanation, an embodiment will now be described in detail with reference to the drawings.

第1図は本発明の一実旌例にかかるVルノマニ電111
J民酸素β度計の断面構造略図をホ1−1図に於て(1
1は市1色とrCろ)口径5閏の白金板、(2)は負I
IIkとなる鉛、(81は電U液となる2〔Jし/eプ
ロピオン酸と3.5モル/eプロピオン酸カリとO1モ
ル/e酸化鉛との混合水溶M、(41は四弗化エチレン
ーエチレンフ千゛リマーからなるI’%さ20μの隔1
1!l、(51はSi1141%11喚(4)をボ゛り
徳化ヒ゛ニール樹11旨製のホルタ−(6)に固定する
fこめの(J−リング、(7)は+E ptI!H1と
吟−(2)との間に介在する抵抗である。
FIG. 1 shows a V Luno Maniden 111 according to an embodiment of the present invention.
A schematic diagram of the cross-sectional structure of the J Civil Oxygen Beta Meter is shown in Figure 1-1 (1
1 is a platinum plate with one color and rCro) diameter 5, (2) is a negative I
Lead to become IIk, (81 is a mixed aqueous solution M of 2 [J / e propionic acid and 3.5 mol / e potassium propionate and O 1 mol / e lead oxide, (41 is tetrafluoride) I'% made of ethylene-ethylene ethylene polymer with a distance of 20μ 1
1! L, (51 is a J-ring, (7) is +EptI!H1, which fixes the Si1141%11 ring (4) to a halter (6) made of a hollowed vinyl tree 11. - (2).

検知71体中の酸素が隔@(4)を透過して市吟(11
0表面に1才ろと、iE肉では前述の(3)式に従う反
応が起こり、透過して釆1こ酸素の准に対応する屯概か
市嘲(1)から負顯(2)へ流れろ。それ故、抵抗(7
)の両端の車庫を油j了することにより酸素の透過域、
換言すれば酸素411を知ることかでさる。
Detection 71 The oxygen in the body permeates through the septum @ (4) and causes Ichigin (11
When the surface of 0 is 1 year old, a reaction according to the above-mentioned formula (3) occurs in the iE meat, and it permeates and flows from the tunshikaichimo (1) to the negative face (2), which corresponds to the atmosphere of oxygen. . Therefore, resistance (7
) by oiling the garages at both ends of the
In other words, it's all about knowing oxygen 411.

次に木尾明にかかる混合電解液の効咀を確かめる1こめ
、1−述[71こものと同型の酸素槽世計4つをill
:I積17、従暇の4モル/e水酸化カリウム71(溶
液2C(:を″11解液とするもの(Al、(Blと本
発明にかかる2モル/eプロピオン酸と3.5モル/e
プロピオン酸カリウムと061モル/l酸化鉛との混合
水溶液2 CCfe電解液とするもの0、Φ)の2種類
の酸素濃度計を製作12、四及びLCIは空気中で、(
I3)及び(1)lは21%酸素、  10%炭酸ガス
、69%窒素の混合ガス中でスを命試験し1こところ、
第2図に示−r、Lうb結果が得られf、:、、。
Next, I checked the effectiveness of the mixed electrolyte on Akira Kio.
: I product 17, free time 4 mol/e potassium hydroxide 71 (solution 2C (: ``11 solution (Al, (Bl and 2 mol/e according to the present invention and propionic acid and 3.5 mol) /e
Mixed aqueous solution of potassium propionate and 061 mol/l lead oxide 2 CCfe electrolyte 0, Φ) Two types of oxygen concentration meters were manufactured 12, 4 and LCI in air (
I3) and (1) were tested in a mixed gas of 21% oxygen, 10% carbon dioxide, and 69% nitrogen.
The results shown in Figure 2 are obtained.

第2図から、促成の/J(峻(ヒ1カリウム水1谷孜を
電1)ゲ牧とrる酸素濃−11は′l〃気中でも5 J
r月θ)寿命(A)シかなく、炭酸カスか10%含土t
Lろ場合に(、t2ケ月弱の(f 命(BI L、かな
いのに比べて、不発明1こ力)かろl毘合水rg FI
Jj’e tl(IQI INとする酸素Q Il[計
tc+、to+番よ、炭酸jjスの11無に係+l !
c < 1%−ff命を!iすること力iわかる。
From Figure 2, the oxygen concentration -11 that is accelerated is 5 J in the atmosphere.
r months θ) Lifespan (A) No carbonate scum or 10% soil content
In the case of L, it will take less than 2 months (f life (BI L, compared to fleeting, non-invention 1).
Jj'e tl (IQI IN and oxygen Q Il [total tc+, to+ number, carbonic acid jj's 11 nothing +l!
c < 1%-ff Life! I understand the power of doing it.

以し詳述しTコ勇1く、不発(1j4は艮尋命でし力〉
もI欠酸Jjスの影響を受けないガルノ〈二’「lI−
41式酸素解1史81を爬供Ij−ろものでちり、その
王π的価irj 1.IBめで大である。
I will explain in detail below, T Koyu 1, misfire (1j 4 is the power of Atsushi no Mikoto)
Garno 〈2'〈lI-
41 formula oxygen solution 1 history 81 is dusted with reptile Ij-romono, its king pi value irj 1. IB is big.

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

第1図は本発明−実雁(夕1jにかかるが)レノ〈二゛
「W池式酸素横I! 、++の断面構造略図をホい;A
 2 :1.を従来品と本発明品との拭@結果の比較を
il< −r 61・・・・ IE晦、 2・・・−・
 負鴎、 3 ・・・1′[畔’tl +4・・・・・
rs嗅、   5・・・−・ O−リンク、6・・・・
・ ホルタ−7・・・・・抵抗、A、Is・・・・従来
品、C,+3・・・・・本発明品。 代理人 弁理士 鈴 木  、彬 方1 図 方7因 呼  町  (R) 丁&、−’t: ?13 ’iK ’jij−二(自:
ffn )昭和57+V:11月11[1 1′1訂庁長官 殿 1、”Jj l’lの表示 昭和574[特6′1願第1278℃)゛倒j2、発明
の名称 カルバ−電池式rlIi索澗瓜G1 代表右   711(須 信 l、(15、補11σ縁
・1℃ 明細i′t1のI14+R’l請求の範囲」及「発明の
詳細な説明」の欄6、補正の内容 (1)明細σ)の特許請求の範囲を下記の)mり補11
Jる。 [酸素を還元りる上で活性の高い金属ししくは金属酸化
物を正極どし、鉛を負極どじ、ブ「1ピAン酸と、アル
カリ金属らしくは72ンU−アの右(幾酸塩と、鉛化合
物との況白水溶液を電解液どしてなることを特徴どづる
気体中あるいは溶液中の酵−素淵度を・測定するための
ガルバニ電池式酸素温石h1゜] (2)明細;S1第4頁第5ft [1+:+ピレン酸
−1を「プロピメン酸」に訂正Jる。 jス 1
Figure 1 shows a schematic diagram of the cross-sectional structure of the present invention - Real Goose (1st January) Reno's ``W Pond Type Oxygen Horizontal I!, ++'';A
2:1. Compare the results of wiping between the conventional product and the product of the present invention.
Negative seaweed, 3...1'[畔'tl +4...
rs smell, 5...--O-link, 6...
- Holter 7...Resistance, A, Is...Conventional product, C, +3...Invention product. Agent Patent Attorney Suzuki, Akikata 1 Matsuoka 7 Inko Machi (R) Ding &, -'t: ? 13 'iK'jij-2 (from:
ffn) Showa 57+V: November 11 [1 1'1 Director-General of the Agency 1, "Jj l'l Display Showa 574 [Special Patent Application No. 6'1 Application No. 1278°C)" 2, name of invention Culver-battery type rlIi Sakuran Gourd G1 Representative Right 711 (Shin Su l, (15, Supplementary 11σ Edge・1℃ Specification i't1 I14+R'l Scope of Claims' and 'Detailed Description of the Invention' Column 6, Contents of Amendment (1) ) Specification σ) Claims below)
Jru. [A metal or metal oxide with high activity in reducing oxygen is used as the positive electrode, and lead is used as the negative electrode. Galvanic cell type oxygen hot stone h1゜] for measuring enzyme depth in gas or solution, characterized by being made by using an aqueous solution of an acid salt and a lead compound as an electrolyte. ) Details; S1, page 4, 5ft [1+:+pyrenic acid-1 is corrected to "propimenic acid".

Claims (1)

【特許請求の範囲】[Claims] 酸素を、@元才る上で活性の高い金属もしくは金属酸化
物をモーと)1、t?を負t4j+とし、プロピレノ酸
と、アルカリ金属もしくはアンモニアの有機酸塩と粉化
合物との混合水m液を1□lf Ill iliとして
なることを特徴とする気体中あるいはm1Il中の酸化
傾度を測疋才ろ1こめのガルバニ゛i’l!、/1.L
J式1俊素濃度計、
Oxygen, with highly active metals or metal oxides) 1. Measure the oxidation gradient in a gas or ml, characterized in that t4j+ is a negative t4j+, and a mixed aqueous liquid of propylenoic acid, an organic acid salt of an alkali metal or ammonia, and a powder compound is 1□lf Ill ili. I'll be the first to know! , /1. L
J type 1 arsenic concentration meter,
JP57127896A 1982-07-21 1982-07-21 Galvanic cell type oxygen concentration meter Granted JPS5917144A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57127896A JPS5917144A (en) 1982-07-21 1982-07-21 Galvanic cell type oxygen concentration meter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57127896A JPS5917144A (en) 1982-07-21 1982-07-21 Galvanic cell type oxygen concentration meter

Publications (2)

Publication Number Publication Date
JPS5917144A true JPS5917144A (en) 1984-01-28
JPH032258B2 JPH032258B2 (en) 1991-01-14

Family

ID=14971337

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57127896A Granted JPS5917144A (en) 1982-07-21 1982-07-21 Galvanic cell type oxygen concentration meter

Country Status (1)

Country Link
JP (1) JPS5917144A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63301208A (en) * 1987-05-30 1988-12-08 Sekisui Chem Co Ltd Polyvinyl acetal resin for adhesive
US4894138A (en) * 1987-09-02 1990-01-16 Dragerwerk Ag Electrochemical gaseous measurement cell

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
THE CHEMICAL ENGINEER=1972 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63301208A (en) * 1987-05-30 1988-12-08 Sekisui Chem Co Ltd Polyvinyl acetal resin for adhesive
US4894138A (en) * 1987-09-02 1990-01-16 Dragerwerk Ag Electrochemical gaseous measurement cell

Also Published As

Publication number Publication date
JPH032258B2 (en) 1991-01-14

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