JPS5917145A - Galvanic cell type oxygen concentration meter - Google Patents
Galvanic cell type oxygen concentration meterInfo
- Publication number
- JPS5917145A JPS5917145A JP57127897A JP12789782A JPS5917145A JP S5917145 A JPS5917145 A JP S5917145A JP 57127897 A JP57127897 A JP 57127897A JP 12789782 A JP12789782 A JP 12789782A JP S5917145 A JPS5917145 A JP S5917145A
- Authority
- JP
- Japan
- Prior art keywords
- acid
- meter
- lead
- oxygen
- acetic acid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/403—Cells and electrode assemblies
- G01N27/404—Cells 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
Landscapes
- 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)
Abstract
Description
【発明の詳細な説明】
本発明はづルバニ電池式酸素碑1(し計の改良に係り、
その目的とするところは、検Ill気体中に含まれる炭
酸ガスの杉情を受けず、かつ野6ηの長い酸素濃1ψ計
を提(Ill trんとするにある、ガルバニ゛?(i
曲式酸素濃度斤1は、一般に手軽で安中さitている。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an improvement of a zurban battery type oxygen meter (1).
The purpose of this is to provide a long oxygen concentration meter with a diameter of 6η that is not sensitive to the effects of carbon dioxide contained in the gas being detected.
The curved oxygen concentration meter is generally convenient and easy to use.
その原理は酸素の「E気化学的鑵元に何効なα属からr
lる正6境と沿からl【ろ負[朔と″r庄解rltと↑
二d己【1日画へのTV&素の4渦を制限するfコめの
隔嘆とから構成さ′+]る酸素−鉛″市油の1F岡と色
画との間に一定の抵抗を接続1−1ことき、そこに流れ
る型面とM/素濃度との間に、直線性があることを利用
し1こものである。The principle is that oxygen's ``E gas has an effect on the chemical origin from the α group.
l positive 6 boundary and along l [ro negative [saku and ″r shōkai rlt and ↑
There is a constant resistance between the 1st floor of the city oil and the color painting consisting of the gap between the two d self [TV to the 1 day painting & the 4 vortices of the element '+] oxygen-lead'' city oil Connection 1-1 takes advantage of the fact that there is linearity between the mold surface flowing there and the M/element concentration.
従来ノカルバニ亀池式酸@濃II□t1には2つの欠点
がある。1つは寿命が6ケ月〜10 ケ月と非常に矩か
いこと、他の1つは比較的晶濃度の炭酸カスを含む検7
i1気体中では使用出来lCい。Conventional Nocarbani Kameike acid@Concentration II□t1 has two drawbacks. One is that it has a very long lifespan of 6 to 10 months, and the other is that it has a relatively long life span of 6 to 10 months.
It cannot be used in i1 gas.
あるいは嘩1幅に前曲が短かくなることである。Or, the previous song may be shortened by one width.
かかる欠点は従来の酸素濃度計が、水酸化カリウムある
いは水酸化ナトリウムのmhアルカリ′11L解液を用
いていることに由来する。This disadvantage arises from the fact that the conventional oxygen concentration meter uses an mh alkaline '11L solution of potassium hydroxide or sodium hydroxide.
以下この4【について説明する。This 4 [ will be explained below.
ガルバニ電池式酸素濃見計にアルカ!J’ %解散を用
いf、:場合、
正答+113では 02−ト21:12(J+4’→4
0[■−・・・・(1)fi嘩T’lJ 2Pb+
4011−+2PbQ千2 +121J + 4 a−
・−+21なる咲応カリCる。負嘩反応生成物でi)ろ
1.” IJ Uはtl(W液中に電解して、沿!物の
表面は稿に更新されろうところが電解液がPI)Uで飽
(11さ1]、ろと、負嘩表面は不働態化さ才1、負(
枳の過“t= +シが増大−する1こめに、1E吟と負
1’l!l!との間【こ流れる?1y醸か変化し、酸#
嘴1(と電流との一足の関係か崩れ、酸素1農度計の寿
命か尽きる。Arca is a galvanic battery type oxygen meter! Using J'% dissolution, if f,:, correct answer +113 is 02-t21:12 (J+4'→4
0[■-・・・(1)fifightT'lJ 2Pb+
4011-+2PbQ 1,0002 +121J + 4 a-
・-+21 Naru Sakio Kali Cru. i) Filtration with the negative reaction product 1. ” IJ U is electrolyzed in tl (W solution, and the surface of the object will be updated to the original, but the electrolyte is PI). 1, negative (
Between 1Egin and negative 1'l!l!, when t=+shi increases, the acid #
The relationship between the beak 1 and the electric current will collapse, and the life of the oxygen 1 agricultural meter will come to an end.
アルカリ電解液を用い1こ従来の1イぐ素m団計のか直
が短かかつrコのは、負碌生成物でJ)る凸OのアJレ
カリノKM液に対するl谷1眸度がf二かtごか01モ
ル/lf@+14−と小さかつ1こからに曲ならない。Using an alkaline electrolyte, the conventional 1 ion group is short and r is a convex O with a negative product. It is as small as f2/t/01 mol/lf@+14- and cannot be bent from one point.
−万検知気体中に叱較的多111の炭酸ガスか含よれて
いるときには矯味では1(ilVFO戸2)式のように
円〕りが生成する代りに不溶性の炭酸鉛(1’ b O
(J 8)あるいは塩基性炭酸鉛(1’b20tJa(
l川)2)がlト成して負陽の過電IFか著しくJ冑入
°tろf:めに、酸素濃IWの測+仁かできなくなる。- When a relatively large amount of carbon dioxide gas is contained in the detected gas, insoluble lead carbonate (1' b O
(J 8) or basic lead carbonate (1'b20tJa (
If the negative overvoltage IF or negative positive overcurrent IF becomes too large, it becomes impossible to measure the oxygen-enriched IW.
このようなアルカリ電解液を用いる従°求の病度計に×
寸し、本発明は、酢酸を=E体とする酸性I捏解ffN
te用いろCとにより、洟が命でしかも炭酸カスの影響
を受け41′いがルバニ電1t12式酸素濃度t1を提
供せんとするものである。For conventional disease diagnosers using such alkaline electrolytes,
Therefore, the present invention is directed to the acidic I-dissolution ffN of acetic acid into the =E form.
By using te and C, it is intended to provide the oxygen concentration t1 of the 41' Lubanian electrician 1t12 type, which is life-threatening and affected by carbon dioxide scum.
かかる濃]尾計の電解液に必要とされる条件は、反応生
r1−物である酸化鉛の溶解度が大きいこと、酸性であ
ること、更にIE励からの水素発生がjjl(いことで
ある。The conditions required for the electrolyte for such a concentrated tail meter are that the solubility of lead oxide, which is a reaction product, is high, that it is acidic, and that hydrogen generation from IE excitation is inhibited. .
これらの条/’1を満足する電解液として、ホーぼり1
1考等は酢酸とアルカリ金14もしくはアンeニアの有
機酸塩と鉛化合物とのa合水屑yW、を発見しfコ。As an electrolyte that satisfies these conditions/'1, Hover 1
The first idea was to discover a mixture of acetic acid, alkali gold 14 or an organic acid salt of annea, and a lead compound, yW.
こ5で云うアルカリ金属とは、カリウム、すトリウム及
びリチウムであり、有機酸とはギ酸、酢酸、プロピオン
酸、醋酸、シュウ酸、マロン酸。The alkali metals referred to in 5 are potassium, strium, and lithium, and the organic acids are formic acid, acetic acid, propionic acid, acetic acid, oxalic acid, and malonic acid.
マイレン酸、コハク酸、グルタル酸、クエン酸。Malenic acid, succinic acid, glutaric acid, citric acid.
クルタミノ酸、A!i石酸、安息香酸、サルチル酸の如
きそのアルカリ金属もしくはアンモニア塩が水に町俗性
の酸であり、鉛化合物とは上記有機酸の鉛塩あるいは酸
化鉛である。Curtaminoic acid, A! The alkali metal or ammonia salts thereof, such as taric acid, benzoic acid, and salicylic acid, are common acids in water, and the lead compounds are lead salts or lead oxides of the above-mentioned organic acids.
まrコ有機峻塩は1挿類に限疋才る必四は4L<、混合
して便tlJ してもよい。The organic salt is limited to one type, but it must be less than 4L, and it may be mixed and used in the stool.
以ド、この弗台水M + +こついて説明する。Below, I will explain the details of this 弗台水M++.
ガルバニ?lj曲式酸素濃度1計に岬性′幌用?欣を用
いfコ鳴合、
市11!11では リ2+40 +4 e →2 H
2U ・・・・(81Mffiiでは 2Pb+
2112(J→21’l+tj+41−1.”−)−4
e −・−・(411【る反応が弓こり、慎重ではア
ルカリ電解?庚の場合と同lI!酸化船(PbU)が生
成する。Galvanic? lj curved oxygen concentration meter for cape style hood? Use kin to f-coarse, ichi 11! In 11, li 2 + 40 + 4 e → 2 H
2U...(2Pb+ for 81Mffii)
2112 (J→21'l+tj+41-1."-)-4
e −・−・(411) The reaction is slow, and if you are careful, the same lI! oxidizer (PbU) as in the case of alkaline electrolysis is generated.
酸化鉛の酢酸水溶液に対する俗解度は、21モル/lで
あり、アルカリ′電解液に14才るそれの21 倍で
ある。喚言すれば、酢酸を電解11にとするlξ蓮1焚
計は従来のそれの21 倍の′Rtii)を有する。The level of understanding of lead oxide in an acetic acid aqueous solution is 21 mol/l, which is 21 times that of an alkaline electrolyte at 14 years old. In other words, the lξren 1-fired meter that uses acetic acid as the electrolyte has a Rtii) that is 21 times that of the conventional one.
次lこi1日f41からの水素!16生tζつぃ−C考
えてみると、市嘲の水素発生平術屯位は欠の(5)式で
与えられろ。Hydrogen from F41 in the next day! 16th grade tζtsui-C If you think about it, the hydrogen generation level of the city is given by the missing formula (5).
En−−0,2412−ト0.05916(log、六
τ1− p’ l (Vvs 8U、I弓)・・+51
ここで、1伯・・・・・ 25′cにおける水桑光生平
+%電位PL−+2・・・・4く素の分用
pi−1・・・ ・・ 直 角ゲ l夜 の 28つt
’+ 15135において pH−1が牛さくノ、、z
JtばなるほどIU:1枳の/に索光牛平盾゛屯位がヒ
1になり、そtしだけ+ll二角ら水系か)b生しゃす
< Iする。酊iす水浴欣のようにρ8が11X六い′
rにLll ilEの場合には、’rf=に低酸素廂1
tJ’ではIE嘲の電イtがかなりキになるので水素が
発生しやすくなる。En--0,2412-to 0.05916 (log, 6τ1-p'l (Vvs 8U, I bow)...+51
Here, 1 bar... 25'c Mitsukuwa Mitsuo average +% potential PL-+2...4 division pi-1... 28 right angles t
'+15135, pH-1 is beef,,z
The more IU: 1, the higher the rank of the Sakuko Gyuhira shield becomes Hi 1, and only then +ll two angles from the water system) b birth. Like a drunken bather, ρ8 is 11x6'
If r is Lll ilE, 'rf = hypoxic area 1
At tJ', the power of IE becomes very strong, so hydrogen is easily generated.
逆にP8が大Aくなれば、正唾の水入iQ生平衡゛ル位
は卑に4fす、水素が発生しにくくζCる。On the other hand, if P8 becomes large A, the water iQ bioequilibrium level of the saliva will be less than 4f, and hydrogen will be less likely to be generated.
そこで酢酸(P″′2〜3)に、弱酸と強111ルとか
らなろ聰、即ち前記の有機酸のアルカリ金1.・穫もし
くはアンモニウム塩を加えていくと+81jJiのpH
は入きくなる。ここで溶液のPhlか7よりも大入<
f(つてアルカリσ<gに移行してしまうと、炭酸if
スの影響を受けるようになるので、pHは7以F、好
ましくは4〜65の範囲に押さえ7・ように才ろことが
肝要である。しっ)シ、浴液のpHを上記16)囲に押
さえ1こだけでは、マtご水素発生の危険が残7)。Therefore, by adding a weak acid and a strong 111 salt, that is, the alkali metal salt or ammonium salt of the above-mentioned organic acid, to acetic acid (P'''2~3), the pH becomes +81JJi.
I'm getting nervous. Here, the Phl of the solution is larger than 7.
f (If the transition to alkaline σ<g occurs, carbonic acid if
It is important to keep the pH below 7F, preferably within the range of 4 to 65, as the pH will be affected by the temperature. However, if you keep the pH of the bath solution within the above 16) range, there is still a risk of hydrogen generation.
−万、鉛の甲衡゛「戎位は次式のように表わさ11El
llンp6” =−0,867+ 0.0296 ”g
(Ph−11v”S” )−’61いて E ”’71
111升・・・・・ 25°Cにおける鉛の平噌電()
□LL +11)4+〕 ・・−・・覗解欣中の沿イ
オノの411【鉛イオンの添IJI口¥1が多ければル
い(Jど、組節の市位、 19! A’ t Jl、ば
正tIIJIの山ニイ11かより員に4〔ることかわか
る、
即ち、沿の平ρ11j I’i’、 イqが7J(素;
6生平衡軍4dまりも直に!、(るまで、上述の混Fa
tt’; Kkに沿イオンを添加してや第1.ば水素
は発生じなくなる。沿イ副〕は酸化鉛もしくは刊機nν
幅の形で添加すtLばよいが、その添加量は水素発生を
回1註できる最少限の1八にすべきである。多すぎると
反応生成物である酸化鉛の溶解1友が減少して寿命か短
か< f、r条。- 10,000, lead's armor ``The position is expressed as the following formula: 11El
p6" = -0,867+ 0.0296 "g
(Ph-11v"S")-'61 and E"'71
111 sho... Lead flat electricity at 25°C ()
□LL +11) 4+〕...411 [Lead ion attachment IJI mouth ¥1 in the peep-understanding is large (Jdo, the city rank of Kumi-Setsu, 19! A' t Jl , it can be seen that from the mountain ni 11 of the base tIIJI, the member is 4[, that is, the flat ρ11j I'i' of the line, iq is 7J (prime;
6th grade equilibrium army 4d Marimo direct! , (until the above-mentioned confusion Fa
tt'; By adding ions along Kk, the first.tt'; If this happens, hydrogen will no longer be generated. ] is lead oxide or printing machine nν
It is sufficient to add it in the form of a width of tL, but the amount added should be 18, which is the minimum amount that can generate hydrogen once. If the amount is too high, the dissolution rate of lead oxide, which is a reaction product, will decrease and the lifespan will be shortened.
かくして得られfこγlル合゛tli、IQ4! /l
+、例えば25モル/g酢酸と4eル/lブロビオノ酸
カリと0.1モル/召酸化希とのτ毘合水1各牧のPす
は62.水系発生平衡電位1.t−0,61V (VS
K:lG>、 H)の’1lSj ”+九イVは一
060v(vs 5CE) ト1! ル。Thus obtained is the total IQ4! /l
+, for example, the combination of 25 mol/g acetic acid, 4 eL/l potassium brobionate, and 0.1 mol/sodium diluted with τ Bi water 1 P sum of each maki is 62. Aqueous system generated equilibrium potential1. t-0,61V (VS
K:lG>, H)'1lSj ''+9iV is 1060v (vs 5CE) To1!ru.
この屁合名孜中では鉛の平衡′11に位の万が水素発生
早衡電位よりも円になるので、iE l+oから卒素が
発生することはない。ま1こ溶液は酸V1.でJ)るか
ら炭酸ガスの影響を受けることもrt <、史に溶液に
はPI)Uの浴解反が大きい酢酸を用いているのでメを
命も長くなる。In this case, the lead equilibrium '11' is more circular than the hydrogen generation equilibrium potential, so no atom is generated from iE l+o. The solution is acid V1. Therefore, the solution is acetic acid, which has a high bath decomposition of PI), so it has a long lifespan.
以上、本発明にか\るカルバニ゛「に池式l′1Ill
!素濃度するfコめ、以IZ−実施例を図面1こ沿って
詳述する。As mentioned above, the Calvany according to the present invention "Niike style l'1Ill
! The IZ-embodiment will now be described in detail with reference to FIG. 1.
第1図は本発明の一実施例にか\るカルバニ屯曲式酸素
繍度tjlの断面構造略1べlを小し、1之に於−〇、
(])はi’E 1ilt+でなるlln ?45 a
ysの白金板、(2)は負j佃とな’) ra 、 (
31It 7fi解故トfl 62.5モル/ e l
!lt、l”a ト4 モル/lプロピオン酸カリと0
1モル/e酸化鉛とのI昆合水(B III 、 (4
1は四弗化エチレンーエチレノコボリマーからなろ厚さ
20μの隔膜、(5)はi’+iJ記隔膜(4)をボ’
J jlX 化ヒ゛= Jしく7i111)(j% 0
) ホIuクー’6) IコIL!Il’rl −t
ルr、=めの0−リン′ノ、(7)はlE film
(1)とt’l llt (2+との間にイr在1ろI
ts抗である。FIG. 1 shows a cross-sectional structure of a carbani tube-type oxygen flow tjl according to an embodiment of the present invention, with a size of about 1 lb.
(]) is i'E 1ilt+lln? 45 a
platinum plate of ys, (2) is negative j Tsukuda') ra, (
31It 7fi solution fl 62.5 mol/e l
! lt, l”a t4 mol/l potassium propionate and 0
I combination water with 1 mol/e lead oxide (B III, (4
1 is a diaphragm made of ethylene tetrafluoride-ethylene copolymer with a thickness of 20μ, and (5) is a diaphragm (4) with i'+iJ.
J jlX conversion = J Shik7i111) (j% 0
) Ho Iu Ku'6) I Ko IL! Il'rl -t
ru r, = 0-rin' ノ, (7) is lE film
(1) and t'l llt (there is an error between 2+ and t'l llt
It is anti-ts.
検゛パ1気体中の酸素が隔膜(4)を透11.情して、
iE Iiii1の表面に達すると、正…では前述の(
8)式にイi白う反応が起こI)、透過して来fこ酸素
の1杖に対応−「る軍旗がjE 111II(11力ラ
MFJjt21へMtt 7.。Detector 1 Oxygen in the gas passes through the diaphragm (4) 11. With compassion,
When it reaches the surface of iE III1, the above-mentioned (
8) A reaction occurs in the formula I), which corresponds to the amount of oxygen that passes through.
そJ″し故、抵抗(7)の1ilIl端のT(f、田を
1lll ’ζすることにマリ、r+?素0) 1’a
ilろα(、換pfitば酸素71、!a度’L”J
ll 7+ことがで、叛る。Therefore, T(f, field 1llll'ζ, r+? elementary 0) 1'a at the 1ilIl end of resistor (7)
ilroα(, if pfit is oxygen 71,!a degree'L"J
ll 7+ to rebel.
欠に本発明にかかる混合電解1f’j O)効果を確か
める1こめ、L・小t、 r、=もの11月型の酸素橢
1u゛計4つを準[4ij L、従来の4モル/e水酸
化カリウム水M欣2 CCを電解液とするもの(Al、
(Blと、不4(=’明にか\る2、5モル/lプロピ
オン酸カリウムと()1モル/l酸化沿との混合水溶液
2 CCを電fQケ欣とするものC)、(切の2jjI
類の酸素順IW別を11′M作し、(Al及び(0)は
空気中で、(均及び(01は21%酸索、 10%炭
酸ガス169%窒素の混合Hス中で寄金試験し1ことこ
ろ1.第21ン1に示すような結果が得ら11.r、:
。第2図から、従来の水酸化カリウム水l谷n記を7j
解液とする酸素ン虐度81は、空気中でも6ケ月の寿命
(A)シかなく1.炭酸ガスが10%含まf’Lる場合
には2ケ月弱のズF +I (IJIしかないのにくら
べて、本発明にかへる混合水溶液を電解Mと才る酸素濃
度旧C+、tD+は炭酸ガスの付熱に係りすく長寿命を
有することがわかる。In order to confirm the effect of the mixed electrolysis according to the present invention, L, small t, r, = one month type oxygen 1u゛, a total of 4 semi-[4ij L, conventional 4 mol/ e Potassium hydroxide water M 2 CC is used as an electrolyte (Al,
(A mixed aqueous solution of Bl, un4(='obviously 2.5 mol/l potassium propionate and () 1 mol/l oxidation solution 2 CC with electric fQ), ( Cut 2jjI
(Al and (0) were grown in the air, and (01 was deposited in a mixed H gas of 21% acid, 10% carbon dioxide, 169% nitrogen). I tested it and got the results as shown in 1.21-1 11.r:
. From Figure 2, we can see that the conventional potassium hydroxide water is 7j
Oxygen concentration 81 as a solution has a lifespan of 6 months (A) even in air. When f'L contains 10% carbon dioxide gas, the oxygen concentration (old C+, tD+) is less than 2 months. It can be seen that it has a long life because it is easily affected by heating of carbon dioxide gas.
以上詳述しfこ如く、本発明は長寿命でしがも炭酸ガス
の影響を受けないガルバニ電/jlJ式酸素濃度g−1
を提供するものであり、その工菫的IIIIl値!へめ
で大である・。As described above in detail, the present invention is a galvanic electric/jlJ type oxygen concentration g-1 which has a long life and is not affected by carbon dioxide gas.
It provides the ultimate value! It's a big deal.
なお、ii、I作成はゲル化して用いてもよい。ま1こ
本願光明の酸素開度計はMγr酸索1鹿反の測定にも1
4用できろ。In addition, in ii and I preparation, it may be used after being gelled. Hongan Komei's oxygen opening meter is also suitable for measuring Mγr acid cables.
You can do it for 4.
ii 1図は本発明一実施例にかかる4jルバニ711
jll1式酸素嗜度の断面1lIIl債略図を示し、第
2図は従>16品と本発明品との寄命試験結4!の比較
を示す。
1 ・ ・ ・ 正 jQ 、 2 −
−− 負 rJ、l 、 3 −=
7[IQ’l iil 。
4・・・・・・l’Mll(il、 5・・・・・
0−リノグ、6・・・・・ポルター。
7・・・・・抵抗、 A、j3・・・・・従来品。
(]、D・・・・本発明品。ii Figure 1 shows a 4J Rubani 711 according to an embodiment of the present invention.
Figure 2 shows a schematic diagram of the cross-section of the oxygen concentration of the jll1 formula, and Figure 2 shows the parasitic test results of the conventional product and the product of the present invention. A comparison is shown. 1 ・ ・ ・ Positive jQ , 2 −
-- Negative rJ, l, 3 -=
7 [IQ'l iil. 4...l'Mll(il, 5...
0-Linogu, 6...Porter. 7...Resistance, A, j3...Conventional product. (], D...Product of the present invention.
Claims (1)
−醇化物からなるIE咄ζ、鉛からなる色画と、電解液
と、酸素4過性隔膜とから十として構成さilろガルバ
ニ゛T1yflu式酸素#llt計に於て、前記電解液
として、酢酸と鉛化合物と史にギ酸、酢酸、プロピオン
酸、酪酸、マレイン酸、クルタミン酸などのfi′機管
のアルカリ金用唱あるいはアンモニウム塩との混防水r
6液を用いてなることを持金とするガルバニ電池式酸素
横+W々(。Oxygen is contained in a liquid containing 10,000 pieces of active leaves, tuna metal or mold, a coloring made of lead, an electrolytic solution, and an oxygen-permeable diaphragm. In the filter galvanic T1yflu type oxygen #llt meter, the electrolytes used include acetic acid and lead compounds, as well as formic acid, acetic acid, propionic acid, butyric acid, maleic acid, curtamic acid, etc. Waterproofing or mixing with ammonium salts
Galvanic cell type oxygen side + W (.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57127897A JPS5917145A (en) | 1982-07-21 | 1982-07-21 | Galvanic cell type oxygen concentration meter |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57127897A JPS5917145A (en) | 1982-07-21 | 1982-07-21 | Galvanic cell type oxygen concentration meter |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS5917145A true JPS5917145A (en) | 1984-01-28 |
Family
ID=14971362
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57127897A Pending JPS5917145A (en) | 1982-07-21 | 1982-07-21 | Galvanic cell type oxygen concentration meter |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5917145A (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58187846A (en) * | 1982-04-27 | 1983-11-02 | Japan Storage Battery Co Ltd | Oxygen densitometer |
-
1982
- 1982-07-21 JP JP57127897A patent/JPS5917145A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58187846A (en) * | 1982-04-27 | 1983-11-02 | Japan Storage Battery Co Ltd | Oxygen densitometer |
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