JPH0439907B2 - - Google Patents

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Publication number
JPH0439907B2
JPH0439907B2 JP23769686A JP23769686A JPH0439907B2 JP H0439907 B2 JPH0439907 B2 JP H0439907B2 JP 23769686 A JP23769686 A JP 23769686A JP 23769686 A JP23769686 A JP 23769686A JP H0439907 B2 JPH0439907 B2 JP H0439907B2
Authority
JP
Japan
Prior art keywords
conductivity
measured
liquid
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.)
Expired
Application number
JP23769686A
Other languages
Japanese (ja)
Other versions
JPS6391544A (en
Inventor
Takeshi Murayama
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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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
て導電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 relates to a method and apparatus for simultaneously measuring electrical conductivity and acid conductivity of a liquid to be measured such as boiler cooling water.

<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、PH、導電率、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、一旦、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
樹脂筒に通し、該筒から溶出する被測定液の酸導
電率を二番目の導電率計で測定するようにしてい
た。また、被測定液を二系統に分流し、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筒
に通し、該筒から溶出する被測定液の酸導電率を
二番目の導電率計で測定するようにしていた。
尚、酸導電率とは、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+
オンとイオン交換してのち導電率計で測定した導
電率のことであつて、カチオン導電率と呼ばれる
こともある。
<Conventional technology> Generally, the water used to rotate turbines used in thermal power generation and nuclear power generation is managed by measuring various parameters such as pH, electrical conductivity, acid conductivity, and hydrazine concentration. There is. especially,
The measurement of electrical conductivity and acid conductivity is important, and conventionally these measurements have been carried out as follows. That is, after first measuring the conductivity of the liquid to be measured using the first conductivity meter, the liquid to be measured is passed through an H + type cation exchange resin cylinder, and the acid conductivity of the liquid to be measured eluted from the cylinder is measured. I was trying to measure it with a second conductivity meter. In addition, the liquid to be measured is divided into two channels, one is led to the first conductivity meter to measure the conductivity of the liquid to be measured, and the other is passed through an H + type cation exchange resin cylinder. A second conductivity meter was used to measure the acid conductivity of the liquid to be measured eluted from the sample.
Note that acid conductivity is the conductivity measured with a conductivity meter after 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 is also 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、酸導電率を
測定するのに上記H+型陽イオン交換樹脂筒に被
測定液を連続的に通過させる必要があつた。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+型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つた。
<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 cylinder in order to measure the acid conductivity. Therefore, the period for the ion exchange resin in the H + type cation exchange resin cylinder to cease to be H + type is short,
There was a drawback that the ion exchange resin had 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+型陽イオン交換筒等の
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を
提供することにある。
The present invention has been made in view of the drawbacks of the conventional examples, and its purpose is to minimize the amount of liquid to be measured, eliminate the need to replace the H + type cation exchange tube, etc. Another object of the present invention is to provide a method and apparatus capable of simultaneously measuring the conductivity and acid conductivity of a liquid to be measured.

<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酸導電率を同時に測
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つて
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 to provide a method and apparatus for simultaneously measuring the electrical conductivity and acid conductivity of a liquid to be measured. After that, the cations in the liquid to be measured are removed by ion exchange using a cation exchange membrane.
The purpose is to detect the acid conductivity of the liquid to be measured after exchanging it with H + ions.

<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、1a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 H2SO4でなるス
キヤベンジヤ液が貯留されている槽、1b,1
c,1eは廃液を貯留する槽、2a,2bはそれ
ぞれ移動相とスキヤベンジヤ液を送液するポン
プ、3は例えば第1〜第6の接続口3a〜3fと
一定内容積(例えば100〜1000μの中の一定容
積)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
オン交換膜チユーブ5aによつて内室5bと外室
5cに区分けされ該外室にH+イオンを含む上記
スキヤベンジヤ液が流され内室5bに上記導電率
計1からの流出液が導びかれるサプレツサ、7は
導電率計4,6およびサプレツサ5を収納しこれ
らを所定温度(例えば45℃)に保つ恒温糟であ
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2aが
駆動すると、槽1a内の移動相は、例えば2ml/
min.(望ましくは0.5〜2.0ml/min.の中の一定流
量)の流量で、ポンプ2a→試料採取弁3の第1
および第2接続口3a,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1d内のスキヤベンジヤ液は、例えば2
ml/min.の流量で、ポンプ2b→サプレツサ5
の外室5c→槽1e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、接続口3f→計量管3g→接続口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、移動相によつて導電率計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つてサプレツサ5の
内室5bに搬入され、陽イオン交換膜チユーブ5
aを介して外室5c内のスキヤベンジヤ液と接液
し、該被測定液中の陽イオンがH+イオンと交換
される。サプレツサ5の内室5bから流出した被
測定液は再び移動相によつて搬送され、導電率計
6によつて酸導電率が検出される。
<Example> Hereinafter, the present invention will be explained in detail using figures. FIG. 1 is an explanatory diagram of the configuration of an embodiment of the present invention,
In the figure, 1a is a tank in which a mobile phase made of, for example, pure water is stored, 1d is a tank in which a scavenge liquid made of, for example, 15 mN H 2 SO 4 is stored, 1b, 1
c and 1e are tanks for storing waste liquid, 2a and 2b are pumps for feeding the mobile phase and scavenge liquid, respectively, and 3 is a tank with a certain internal volume (for example, 100 to 1000 μm) connected to the first to sixth connection ports 3a to 3f. 4 and 6 are conductivity meters, and 5 is a cation exchange membrane inside. Suppressor 7, which is divided into an inner chamber 5b and an outer chamber 5c by a tube 5a, in which the scavenging liquid containing H + ions flows, and the effluent from the conductivity meter 1 is guided into the inner chamber 5b. is a constant temperature chamber that houses the conductivity meters 4, 6 and the suppressor 5 and maintains 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 2a is driven, the mobile phase in the tank 1a is, for example, 2 ml/
min. (preferably a constant flow rate between 0.5 and 2.0 ml/min.), the pump 2a → the first sample sampling valve 3
and second connection ports 3a, 3b→conductivity meter 4→inner chamber 5b of suppressor 5→conductivity meter 6, and then through tank 1b
It flows in a channel that leads to. Further, when the pump 2b is driven, the scavenge liquid in the tank 1d is, for example, 2
At a flow rate of ml/min., pump 2b → suppressor 5
It flows through a flow path from the outer chamber 5c to the tank 1e. Furthermore,
The liquid to be measured is injected from the connection port 3e of the sample sampling valve 3, flows along the path of connection port 3f→metering tube 3g→connection port 3c→connection port 3d→tank 1c, and fills the inside of the metering 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 is transferred to the cation exchange membrane tube 5.
It comes into contact with the scavenger liquid in the outer chamber 5c through the channel a, and the cations in the liquid to be measured are exchanged with H + ions. The liquid to be measured flowing out of the inner chamber 5b of the suppressor 5 is transported again by the mobile phase, and the acid conductivity 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(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クであつて被
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つて被測定液の酸導
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(Nacl)溶液0.28ミリ当量/
を100μ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導水を用いたとき
のクロマトグラムである。第2図や第3図のクロ
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酸導電率がピーク
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 represents conductivity (units are μs/cm). Further, A is a peak based on the detection signal of the conductivity meter 4 and indicates the conductivity of the liquid to be measured, and B is a peak based on the detection signal of the conductivity meter 6 and indicates the acidity of the liquid to be measured. Shows conductivity. In addition, Fig. 2 shows a sodium chloride (NaCl) solution of 0.28 milliequivalents as the liquid to be measured.
This is a chromatogram obtained by injecting 100μ of . As is clear from the chromatograms in FIGS. 2 and 3, according to the embodiment of the present invention, the conductivity and acid 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+
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100〜
1000μ)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、サプレツサ5の外室5cには
常時スキヤベンジヤ液が流れていて陽イオン交換
膜チユーブ5a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筒のような再
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 + type cation column, etc., and the conductivity of the liquid to be measured is reduced. A method and apparatus capable of simultaneously measuring acid conductivity and acid conductivity are realized. That is, an amount sufficient to fill 3 g of the measuring tube of the sampling valve 3 (usually 100 ~
Only 1000μ) of the liquid to be measured is required.
The required amount of the liquid to be measured is extremely small compared to the conventional example. In addition, since the scavenge liquid is constantly flowing in the outer chamber 5c of the suppressor 5 and the cation exchange membrane tube 5a is kept in the H + type, it is not possible to regenerate it like the H + type cation exchange resin tube in the conventional example. No operation or replacement is required. 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. Incidentally, the conductivity meters 4 and 6 are as follows:
It is also possible to use it with a normal 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 drawings]

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。 1a〜1e……槽、2a,2b……ポンプ、3
……試料採取弁、4,6……導電率計、5……サ
プレツサ、7……恒温槽。
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. 1a to 1e...tank, 2a, 2b...pump, 3
... Sample collection valve, 4, 6 ... Conductivity meter, 5 ... Suppressor, 7 ... Constant temperature bath.

Claims (1)

【特許請求の範囲】 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つてH+
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。 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ユーブによつて内室と外室
に区分けされ該外室にH+イオンを含むスキヤベ
ンジヤ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ツサと、該サプレツ
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。
[Scope of Claims] 1. A certain amount of the liquid to be measured is sampled, the conductivity of the liquid to be measured is detected, and then the cations in the liquid to be measured are converted to H + by ion exchange using a cation exchange membrane. A method for measuring electrical conductivity and acid conductivity, characterized in that the conductivity and acid conductivity of the liquid to be measured are simultaneously measured by exchanging with ions and then detecting the acid conductivity of the liquid to be measured. 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 for flowing a scavenge liquid containing H + ions into an outer chamber and guiding the effluent from the first conductivity meter to the inner chamber; and a second suppressor for detecting the conductivity of the fluid eluted from the inner chamber of the suppressor. a conductivity meter, and the conductivity and acid conductivity of the liquid to be measured are simultaneously measured by measuring the acid conductivity of the liquid to be measured with the second conductivity meter. Measuring device for rate 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 JPS6391544A (en) 1988-04-22
JPH0439907B2 true 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)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5729488B2 (en) * 2011-12-16 2015-06-03 株式会社島津製作所 Ion chromatograph

Also Published As

Publication number Publication date
JPS6391544A (en) 1988-04-22

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