JPS6391544A - Method and apparatus for measuring conductivity and acid conductivity - Google Patents

Method and apparatus for measuring conductivity and acid conductivity

Info

Publication number
JPS6391544A
JPS6391544A JP23769686A JP23769686A JPS6391544A JP S6391544 A JPS6391544 A JP S6391544A JP 23769686 A JP23769686 A JP 23769686A JP 23769686 A JP23769686 A JP 23769686A JP S6391544 A JPS6391544 A JP S6391544A
Authority
JP
Japan
Prior art keywords
conductivity
liquid
measured
acid
meter
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
JP23769686A
Other languages
Japanese (ja)
Other versions
JPH0439907B2 (en
Inventor
Takeshi Murayama
健 村山
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.)
Yokogawa Electric Corp
Original Assignee
Yokogawa 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 Yokogawa Electric Corp filed Critical Yokogawa Electric Corp
Priority to JP23769686A priority Critical patent/JPS6391544A/en
Publication of JPS6391544A publication Critical patent/JPS6391544A/en
Publication of JPH0439907B2 publication Critical patent/JPH0439907B2/ja
Granted legal-status Critical Current

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  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)

Abstract

PURPOSE:To reduce a necessary amount of a liquid to be measured, by detecting the conductivity of the liquid to be measured and subsequently exchanging a cation with an H<+>-ion before detecting acid conductivity. CONSTITUTION:The mobile phase in a tank 1a flows through the route of a pump 2a the connection ports 3a, 3b of a specimen sampling valve 3 a conductivity meter 4 the inner chamber 5b of a suppressor 5 a conductivity meter 6. The scavenger liquid in a tank 1d flows through the route of pump 2b an outer chamber 5c a tank 1e and a liquid to be measured is injected from a connection port 3e to flow through the route of a connection port 3f a weighing pipe 3g a connection port 3c a connection port 3d a tank 1c to fill the weighing pipe 3g. When the sampling valve 3 is turned On, a flow passage is changed over from a solid line to a broken line and the liquid to be measured is fed to the conductivity meter 4 to detect the conductivity of the liquid to be measured. Then, the liquid to be measured is sent in the inner chamber 5b of the suppressor 5 to be contacted with the scavenger liquid in the outer chamber 5c through a cation exchange membrane tube 5a and a cation is exchanged with an H<+>-ion and acid conductivity is detected by the conduc tivity meter 6.

Description

【発明の詳細な説明】 〈産業上の利用分野〉 本発明は、ボイラ冷却水などの被測定液について導′I
L率と酸導電率を同時に測定する方法およびその装置に
関する。
DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention provides a guide for measuring liquids such as boiler cooling water.
The present invention relates to a method and apparatus for simultaneously measuring L ratio and acid conductivity.

〈従来の技術〉 一般に、火力発電や原子力発電で使用されるタービンを
回転させるための水は、pHj導電率。
<Prior art> In general, the water used to rotate the turbines used in thermal power generation and nuclear power generation has a conductivity of pHj.

酸導電率、およびヒドラジン濃度等の各種パラメータを
測定しながら管理が行なわれている。特に、導電率と酸
導電率の測定は重要であり、従来、次のようにしてそれ
らの測定が行なわれていた。即ち、−旦、最初の導電率
計で被測定液の導電率を測定したのち、該被測定液をH
”型陽イオン交換樹脂簡に通し、線間から溶出する被測
定液の酸導電率を二番目の4電率計で測定するようにし
ていた。また、被測定液を一系統に分流し、一方を最初
の導電率計に導びいて該被測定液の導電率を測定すると
共に、他方をH+型陽イオン交換樹脂簡に通し、線間か
ら溶出する被測定液の巖導電率を二番目の導電率計で測
定するようにqでいた。尚、r11導電率とは、被測定
液をH+型陽イオン交換樹脂筒に通し、被測定液中の陽
イオンをH+イオンとイオン交換してのち導電率計で測
定した導電率のことであって、カチオン導電率と呼ばれ
ることもある。
Management is carried out by measuring various parameters such as acid conductivity and hydrazine concentration. In particular, the measurement of electrical conductivity and acid conductivity is important, and conventionally these measurements have been carried out as follows. That is, after measuring the conductivity of the liquid to be measured with the first conductivity meter, the liquid to be measured is heated to
The acid conductivity of the liquid to be measured passed through a cation exchange resin tube and eluted from between the lines was measured using a second 4-conductivity meter.Also, the liquid to be measured was divided into one system, One side is led to the first conductivity meter to measure the conductivity of the liquid to be measured, and the other is passed through H+ type cation exchange resin, and the conductivity of the liquid to be measured eluted from between the lines is measured to the second one. q as measured by a conductivity meter.The r11 conductivity is measured by passing the liquid to be measured through an H+ type cation exchange resin cylinder and exchanging the cations in the liquid with H+ ions. It refers to the electrical conductivity measured using a conductivity meter, and is sometimes called cationic conductivity.

〈発明が解決しようとする問題点〉 然し乍ら、上記従来例においては、耐湯電率を測定する
のに上記H+型陽イオン交換樹脂簡に被測定液を連続的
に通過させる必要があった。このため、上記H+型陽イ
オン交換樹脂筒内のイオン交換樹脂がH+壓でなくなる
ための期間が短かく、該イオン交換樹脂を再生させたり
新品と交換したりする必要があるという欠点があった。
<Problems to be Solved by the Invention> However, in the conventional example described above, it was necessary to continuously pass the liquid to be measured through the H+ type cation exchange resin in order to measure the electrical resistance. For this reason, the period during which the ion exchange resin in the H+ type cation exchange resin cylinder ceases to be an H+ cylinder is short, and there is a drawback that the ion exchange resin needs to be regenerated or replaced with a new one. .

本発明はかかる従来例の欠点に鑑みてなされたものであ
り、その目的は、被測定液の必要量が極少量であると共
に上記H”l+陽イオン交換簡等の交換が不要であり、
且つ、被測定液の導電率と耐湯電率が同時に測定できる
方法およびその装置を提供することにある。
The present invention has been made in view of the drawbacks of the conventional example, and its purpose is to minimize the amount of liquid to be measured and to eliminate the need to replace the H"l+ cation exchange strip, etc.
Another object of the present invention is to provide a method and apparatus capable of simultaneously measuring the electrical conductivity and electrical resistance of a liquid to be measured.

く問題点を解決するための手段〉 上述のような問題点を解決する本発明の特徴は、被測定
液の導電率および耐湯電率を同時に測定する方法および
その装置において、被測定液の導電率を検出し、その後
、該被測定液中の陽イオンを陽イオン交換膜を用いるイ
オン交換によってH+イオンと交換してのち該被測定液
の酸4電率を検出するようにしたことにある。
Means for Solving the Problems> A feature of the present invention that solves the above-mentioned problems is a method and apparatus for simultaneously measuring the electrical conductivity and hot water resistance of a liquid to be measured. The conductivity is detected, and then the cations in the liquid to be measured are exchanged with H+ ions by ion exchange using a cation exchange membrane, and then the acid tetraelectricity of the liquid to be measured is detected. be.

〈実施例〉 以下、本発明について図を用いて詳しく説明する。第1
図は本発明実施例の構成説明図であり、図中、I@は例
えば純水でなる移動相が貯留されている槽、1dは例え
ば15mN HgSO4でなるスキャベンジャ液が貯留
されている槽、Ib、lc、leは廃液を貯留する槽、
2s、2bはそれぞれ移動相とスキャベンジャ液を送液
するポンプ、3は例えば第1〜第6の接続口31〜3f
と一定の内容積(例えば 100〜1000μ2の中の
一定容植)を有する計量管3gを有しその内部流路が実
線接続状態と破線接続状態に交互に切換えられる試料採
取弁、4,6は導電率計、5は内部が陽イオン交換膜チ
ューブ5Kによって内室5bと外室5cに区分けされ該
外室にH+イオンを含む上記スキャベンジャ液が流され
内室5bに上記導電率計1からの流出液が導びかれるサ
プレッサ、7は導電率計4,6およびサプレッサ5を収
納しこれらを所定温度(例えば45°C)に保つ恒温槽
である。尚、移動相の導電率は被測定液の導電率に比し
て通常 1/100程度となるように選択され、通常、
移動相として純水が使用される。このような構成からな
る本発明の実施例において、ポンプ21が駆動すると、
槽り内の移動相は、例えば2mR/zin、  (望ま
しくは0.5〜2.0 mN/win、の中の一定流量
)の流量で、ポンプ2I→試料採取弁3の第1および第
2接続口3*、 3b→導電率計4→サプレツサ5の内
室5b→導電率計6を通り、槽1bに至る流路で流れる
。また、ポンプ2bが駆動すると、槽Id内のスキャベ
ンジャ液は、例えば2d/win。
<Example> Hereinafter, the present invention will be explained in detail using the drawings. 1st
The figure is an explanatory diagram of the configuration of an embodiment of the present invention, in which I@ is a tank in which a mobile phase made of, for example, pure water is stored, 1d is a tank in which a scavenger liquid made of, for example, 15 mN HgSO4 is stored, Ib, lc, le are tanks for storing waste liquid,
2s and 2b are pumps that feed the mobile phase and scavenger liquid, respectively; 3 is, for example, the first to sixth connection ports 31 to 3f;
and a sampling valve 4, 6 which has a metering tube 3g having a constant internal volume (for example, a constant volume of 100 to 1000 μ2) and whose internal flow path is alternately switched between a solid line connection state and a broken line connection state; The conductivity meter 5 is divided into an inner chamber 5b and an outer chamber 5c by a cation exchange membrane tube 5K, and the scavenger liquid containing H+ ions is flowed into the outer chamber, and the conductivity meter 1 is divided into the inner chamber 5b. The suppressor 7 to which the effluent is introduced is a constant temperature bath that houses the conductivity meters 4, 6 and the suppressor 5 and keeps them at a predetermined temperature (for example, 45° C.). The conductivity of the mobile phase is usually selected to be about 1/100 of the conductivity of the liquid to be measured.
Pure water is used as the mobile phase. In the embodiment of the present invention having such a configuration, when the pump 21 is driven,
The mobile phase in the tank is pumped from the pump 2I to the first and second sampling valves 3 at a flow rate of, for example, 2 mR/zin (preferably a constant flow rate of 0.5 to 2.0 mN/win). The flow passes through the connection ports 3* and 3b → the conductivity meter 4 → the inner chamber 5b of the suppressor 5 → the conductivity meter 6, and flows in the flow path leading to the tank 1b. Further, when the pump 2b is driven, the scavenger liquid in the tank Id is, for example, 2d/win.

の流量で、ポンプ2b→サプレツサ5の外室5 c =
 Pa1eに至る流路で流れる。更に、被測定液が、試
料採取弁3の接続口3eから注入され、接続ロ3f→計
量管3g+接続ロ3c→接続口3d−+槽1cの経路で
流れ、計量管3g内を満たす。この状態で、試料採取弁
3がオンにされると、その内部流路が実線接続状態から
破線接続状態に切換えられる。このため、計量管3g内
の被測定液は、移動相によって導電率計4に搬送されそ
の導電率が検出される。該導電率計4から流出した被測
定液は移動相によってサプレッサ5の内室5bに搬入さ
れ、陽イオン交換膜チューブ51を介して外室5c内の
スキャベンジャ液と接液し、該被測定液中の陽イオンが
H+イオンと交換される。サプレッサ5の内室5bから
流出した被測定液は再び移動相によって搬送され、導電
率計6によって耐湯電率が検出される。
At the flow rate of pump 2b→outer chamber 5c of suppressor 5 =
It flows in the channel leading to Pa1e. Further, the liquid to be measured is injected from the connection port 3e of the sample sampling valve 3, flows along the path of connection hole 3f -> measuring tube 3g + connection hole 3c -> connection port 3d - + tank 1c, filling the inside of the measuring tube 3g. When the sample collection valve 3 is turned on in this state, its internal flow path is switched from the solid line connection state to the broken line connection state. Therefore, the liquid to be measured in the measuring tube 3g is conveyed to the conductivity meter 4 by the mobile phase, and its conductivity is detected. The liquid to be measured flowing out of the conductivity meter 4 is carried into the inner chamber 5b of the suppressor 5 by the mobile phase, and comes into contact with the scavenger liquid in the outer chamber 5c via the cation exchange membrane tube 51. Cations in the liquid are exchanged with H+ ions. The liquid to be measured that has flowed out from the inner chamber 5b of the suppressor 5 is transported again by the mobile phase, and the electrical conductivity of the hot water is detected by the conductivity meter 6.

第2図および第3図は上述のようにして検出された導電
率計4,6の検出信号を図示しない記録計に導いて描か
せたクロマトグラムであり、図中、横軸は時間T(単位
は分)を示し縦軸は導電率υ(単位はμs/cm)を示
している。また、Aは導電率計4の検出信号に基ずくピ
ーbであって被測定液の導電率を示しており、Bは導電
率計6の検出信号に基ずくピークであって被測定液の酸
導電率を示している。尚、第2図は被測定液として塩化
ナトリウム(LC(i)溶液0.28ミリ当量/iを 
1oftμg注入して得られたクロマトグラムであり、
第3図は被測定液として水運水を用いたときのクロマト
グラムである。第2図や第3図めクロマトグラムから明
らかなように、本発明実施例によれば、被測定液の導電
率と峻導電率がピークA、Bに基いて正確に測定できる
ようになる。
2 and 3 are chromatograms drawn by guiding the detection signals of the conductivity meters 4 and 6 detected as described above to a recorder (not shown). In the figures, the horizontal axis is the time T ( The unit is minutes), and the vertical axis is the conductivity υ (units are μs/cm). Further, A is a peak b based on the detection signal of the conductivity meter 4, which indicates the conductivity of the liquid to be measured, and B is a peak based on the detection signal of the conductivity meter 6, which indicates the conductivity of the liquid to be measured. Acid conductivity is shown. In addition, Fig. 2 shows sodium chloride (LC(i) solution 0.28 meq/i as the liquid to be measured).
This is a chromatogram obtained by injecting 1ofμg,
FIG. 3 is a chromatogram when water is used as the liquid to be measured. As is clear from the chromatograms in FIGS. 2 and 3, according to the embodiment of the present invention, the conductivity and steep conductivity of the liquid to be measured can be accurately measured based on peaks A and B.

〈発明の効果〉 以上詳しく説明したような本発明によれば、被測定液の
必要量が極めて少量であると共にH+z陽イオンカラム
等の交換が不要であり、且つ、被測定液の導電率と酸導
電率が同時に測定できる方法およびその装置が実現する
。即ち、試料採取弁3の計量管3gを満たすに十分な量
(通常1011〜1008μm)の被測定液が必要なだ
けであるため、被測定液の必要量が前記従来例の場合に
比して極めて少ない。また、サプレッサ5の外室5cに
は常時スキャベンジャ液が流れていて陽イオン交換膜チ
ューブ51がH+型に保たれているため、前記従来例の
H+型陽イオン交換樹脂尚のような再生操作や交換等が
不要である。更に、導電率計4,6を用いて同一被測定
液の導電率と酸導電率を測定するため、被測定液の導電
率と酸導電率を同時に測定できる。尚、上記導電率計4
.6は、被測定液中の陰イオンや陽イオンを測定するた
めに使用される通常の導電率計で共用することも可能で
ある。
<Effects of the Invention> According to the present invention as described in detail above, the required amount of the liquid to be measured is extremely small, there is no need to replace the H+z cation column, etc., and the conductivity of the liquid to be measured and the A method and apparatus capable of simultaneously measuring acid conductivity are realized. That is, since only a sufficient amount (usually 1011 to 1008 μm) of the liquid to be measured is required to fill the measuring tube 3g of the sample sampling valve 3, the required amount of the liquid to be measured is smaller than that in the conventional example. Very few. In addition, since the scavenger liquid is constantly flowing in the outer chamber 5c of the suppressor 5 and the cation exchange membrane tube 51 is maintained in the H+ type, the regeneration operation of the H+ type cation exchange resin of the conventional example is not necessary. There is no need for replacement or replacement. Furthermore, since the conductivity meters 4 and 6 are used to measure the conductivity and acid conductivity of the same liquid to be measured, the conductivity and acid conductivity of the liquid to be measured can be measured simultaneously. In addition, the above conductivity meter 4
.. 6 can also be used in common with an ordinary conductivity meter used to measure anions and cations in a liquid to be measured.

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

第1図は本発明実施例の構成説明図であり、第2図およ
び第3図は本発明実施例を用いて作成したクロマトグラ
ムである。 1鳳〜1c・・・槽、2i、 2b・・・ポンプ、3・
・・試料採取弁、4.6・・・導電率計、5・・・サプ
レッサ、7・・・恒温槽。 第7図 第3図 T(vLn)
FIG. 1 is an explanatory diagram of the configuration of an embodiment of the present invention, and FIGS. 2 and 3 are chromatograms created using the embodiment of the present invention. 1-1c...tank, 2i, 2b...pump, 3.
... Sampling valve, 4.6... Conductivity meter, 5... Suppressor, 7... Constant temperature bath. Figure 7 Figure 3 T (vLn)

Claims (2)

【特許請求の範囲】[Claims] (1)被測定液を一定量採取し該被測定液の導電率を検
出し、その後、該被測定液中の陽イオンを陽イオン交換
膜を用いるイオン交換によってH^+イオンと交換して
のち該被測定液の酸導電率を検出することにより、前記
被測定液の導電率と酸導電率を同時に測定することを特
徴とする導電率と酸導電率の測定方法。
(1) Collect a certain amount of the liquid to be measured, detect the conductivity of the liquid to be measured, and then exchange the cations in the liquid to H^+ ions by ion exchange using a cation exchange membrane. A method for measuring electrical conductivity and acid conductivity, characterized in that the electrical conductivity and acid conductivity of the liquid to be measured are simultaneously measured by subsequently detecting the acid conductivity of the liquid to be measured.
(2)被測定液を一定量採取する試料採取弁と、該被測
定液の導電率を測定する第1導電率計と、内部が陽イオ
ン交換膜チューブによって内室と外室に区分けされ該外
室にH^+イオンを含むスキャベンジャ液を流すと共に
前記第1導電率計からの流出液を該内室に導びくサプレ
ッサと、該サプレッサの内室から溶出する流体の導電率
を検出する第2導電率計とを具備し、該第2導電率計で
前記被測定液の酸導電率を測定することにより、前記被
測定液の導電率と酸導電率を同時に測定することを特徴
とする導電率と酸導電率の測定装置。
(2) A sample collection valve that collects a certain amount of the liquid to be measured, a first conductivity meter that measures the conductivity of the liquid to be measured, and a cation exchange membrane tube that divides the interior into an inner chamber and an outer chamber. A suppressor that flows a scavenger liquid containing H^+ ions into the outer chamber and guides the effluent from the first conductivity meter to the inner chamber, and detects the conductivity of the fluid eluted from the inner chamber of the suppressor. and a second conductivity meter, and by measuring the acid conductivity of the liquid to be measured with the second conductivity meter, the conductivity and acid conductivity of the liquid to be measured are simultaneously measured. Measuring device for electrical conductivity and acid conductivity.
JP23769686A 1986-10-06 1986-10-06 Method and apparatus for measuring conductivity and acid conductivity Granted JPS6391544A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23769686A JPS6391544A (en) 1986-10-06 1986-10-06 Method and apparatus for measuring conductivity and acid conductivity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23769686A JPS6391544A (en) 1986-10-06 1986-10-06 Method and apparatus for measuring conductivity and acid conductivity

Publications (2)

Publication Number Publication Date
JPS6391544A true JPS6391544A (en) 1988-04-22
JPH0439907B2 JPH0439907B2 (en) 1992-07-01

Family

ID=17019155

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23769686A Granted JPS6391544A (en) 1986-10-06 1986-10-06 Method and apparatus for measuring conductivity and acid conductivity

Country Status (1)

Country Link
JP (1) JPS6391544A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013088834A1 (en) * 2011-12-16 2013-06-20 株式会社島津製作所 Ion chromatograph

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013088834A1 (en) * 2011-12-16 2013-06-20 株式会社島津製作所 Ion chromatograph
JPWO2013088834A1 (en) * 2011-12-16 2015-04-27 株式会社島津製作所 Ion chromatograph
US9535034B2 (en) 2011-12-16 2017-01-03 Shimadzu Corporation Ion chromatograph

Also Published As

Publication number Publication date
JPH0439907B2 (en) 1992-07-01

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