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JPS5810480B2 - Method for controlling electrical conductivity of electroplating bath - Google Patents
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JPS5810480B2 - Method for controlling electrical conductivity of electroplating bath - Google Patents

Method for controlling electrical conductivity of electroplating bath

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Publication number
JPS5810480B2
JPS5810480B2 JP55138581A JP13858180A JPS5810480B2 JP S5810480 B2 JPS5810480 B2 JP S5810480B2 JP 55138581 A JP55138581 A JP 55138581A JP 13858180 A JP13858180 A JP 13858180A JP S5810480 B2 JPS5810480 B2 JP S5810480B2
Authority
JP
Japan
Prior art keywords
electrical conductivity
concentration
mirabilite
liquid
bath
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
JP55138581A
Other languages
Japanese (ja)
Other versions
JPS5763699A (en
Inventor
石田幸男
中瀬郁夫
島村耕市
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.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries Ltd
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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP55138581A priority Critical patent/JPS5810480B2/en
Publication of JPS5763699A publication Critical patent/JPS5763699A/en
Publication of JPS5810480B2 publication Critical patent/JPS5810480B2/en
Expired legal-status Critical Current

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  • Electroplating Methods And Accessories (AREA)

Description

【発明の詳細な説明】 この発明は、鋼板等の電気鍍金においてその鍍金浴の電
気伝導度を高く保持する制御方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a control method for maintaining high electrical conductivity of a plating bath during electroplating of steel plates and the like.

従来から電気鍍金浴中の電気伝導度を高く調整して鍍金
に使用する電力の消費を少なくする方法がとられている
Conventionally, methods have been used to reduce the consumption of electric power used for plating by adjusting the electrical conductivity in an electroplating bath to be high.

この電気伝導度の調整には浴液中に芒硝(Na2SO,
)を添加して調整するのが一般的であるが、鍍金浴液便
用中に添加された芒硝は、日を経過するに従い芒硝が流
出して濃度が低下し使用電力が増大するため数日間隔毎
に一定量の芒硝を補充添加する方法がなされている。
To adjust the electrical conductivity, add sodium sulfate (Na2SO,
) is commonly added to the plating bath liquid. However, as the days pass, the sodium sulfate that is added to the plating bath liquid flows out, the concentration decreases, and the power consumption increases, so it may take several days. A method is used in which a fixed amount of Glauber's salt is added at regular intervals.

この芒硝の調整については芒硝の含有量が多すぎると鍍
金鋼板表面に付着して鋼板の品質を害し、又含有量が少
ないと電気伝導度が低下して消費電力を増大させるとい
う問題がある。
Regarding the adjustment of mirabilite, there is a problem that if the content of mirabilite is too high, it will adhere to the surface of the plated steel sheet and impair the quality of the steel sheet, and if the content is too low, the electrical conductivity will decrease and power consumption will increase.

この発明は、鍍金浴の電気伝導度を鋼板の品質と消費電
力のバランスを考えて理想的に管理する制御方法を提案
するもので、その要旨は、電気鍍金浴中の電気伝導度と
浴液温度および水素イオン濃度を測定し、これらの測定
値から電気伝導度調整剤の添加量を制御することを特徴
とするものである。
This invention proposes a control method to ideally manage the electrical conductivity of the electroplating bath by considering the balance between the quality of the steel sheet and the power consumption. This method is characterized by measuring temperature and hydrogen ion concentration, and controlling the amount of electrical conductivity regulator added based on these measured values.

本発明者等は鋼板の電気鍍金浴液中の電気伝導度につい
て種々研究した結果浴液中の電気伝導度は夜中の芒硝の
濃度、浴液の温度、浴液の水素イオン濃度(PH)によ
って大きく変化することを見出した。
The present inventors have conducted various studies on the electrical conductivity in the electroplating bath solution for steel sheets. As a result, the electrical conductivity in the bath solution depends on the concentration of Glauber's salt during the night, the temperature of the bath solution, and the hydrogen ion concentration (PH) of the bath solution. I found that there was a big change.

第1図、第2図、第3図は浴液中の芒硝濃度が変化する
経過、温度、水素イオン濃度(PH)により液中の電気
伝導度が変化する状態を示す図である。
FIGS. 1, 2, and 3 are diagrams showing how the concentration of mirabilite in the bath liquid changes, and how the electrical conductivity in the liquid changes depending on temperature and hydrogen ion concentration (PH).

横軸は時間の経過であり、縦軸は浴液中の電気伝導度、
液温度、水素イオン濃度である。
The horizontal axis is the passage of time, and the vertical axis is the electrical conductivity in the bath liquid.
These are liquid temperature and hydrogen ion concentration.

図中曲線aは電気伝導度の変化曲線であり、曲線すは浴
液の温度曲線であり、曲線Cは液中の水素イオン濃1(
PH)の変化曲線である。
In the figure, curve a is the change curve of electrical conductivity, curve 2 is the temperature curve of the bath liquid, and curve C is the hydrogen ion concentration 1 (
PH) change curve.

第1図において、電気伝導度曲線aは芒硝を含む浴液が
浴液中に芒硝を約1.4時間経過後添加したときの状態
を示し芒硝濃度が20g/lであったのが、芒硝の添加
により399/lに変化した場合を示し芒硝の添加によ
り夜の電気伝導度は上昇することを示している。
In Figure 1, electrical conductivity curve a shows the state of the bath solution containing mirabilite when mirabilite was added to the bath solution after approximately 1.4 hours. This shows that the electrical conductivity at night changes to 399/l with the addition of Glauber's salt.

第2図において、液の水素イオン濃度曲線Cは約50分
経過後PH値を2.7から2.3に下げた場合の電気伝
導度曲線aを示すもので、水素イオン濃度は低い程電気
伝導度は上昇することを示している。
In Figure 2, the hydrogen ion concentration curve C of the liquid shows the electrical conductivity curve a when the pH value is lowered from 2.7 to 2.3 after about 50 minutes, and the lower the hydrogen ion concentration, the more electrical conductivity. The conductivity is shown to increase.

又第3図においては、浴液の温度曲線すと電気伝導度曲
線aとの対比を示すもので、明らかに浴液温度が上昇す
ると液中の電気伝導度が上昇することを示している。
Furthermore, FIG. 3 shows a comparison between the temperature curve of the bath liquid and the electrical conductivity curve a, clearly showing that as the temperature of the bath liquid increases, the electrical conductivity in the liquid increases.

このような知見にもとづき更に詳しくその関係を調査し
た。
Based on this knowledge, we investigated the relationship in more detail.

第4図は液中の芒硝濃度と電気伝導度の関係を示す図で
ある。
FIG. 4 is a diagram showing the relationship between the concentration of mirabilite in the liquid and the electrical conductivity.

横軸は液中の芒硝濃度を示し、縦軸は電気伝導度である
The horizontal axis shows the concentration of mirabilite in the liquid, and the vertical axis shows the electrical conductivity.

図で明らかなように芒硝濃度と電気伝導度は強い相関を
示している。
As is clear from the figure, there is a strong correlation between mirabilite concentration and electrical conductivity.

第5図は、PH値2,5のときの芒硝各濃度における液
温度と電気伝導度の関係を示す図である。
FIG. 5 is a diagram showing the relationship between liquid temperature and electrical conductivity at various concentrations of mirabilite at pH values of 2 and 5.

図で明らかのように液温と電気伝導度についても直線的
関係があることを示している。
As is clear from the figure, there is also a linear relationship between liquid temperature and electrical conductivity.

又第6図は液の水素イオン濃度(PH値)と電気伝導度
の関係図である。
FIG. 6 is a diagram showing the relationship between the hydrogen ion concentration (PH value) and electrical conductivity of the liquid.

横軸は水素イオン濃度(PH)であり、縦軸は電気伝導
度である。
The horizontal axis is hydrogen ion concentration (PH), and the vertical axis is electrical conductivity.

図で明らかのように芒硝濃度および液温度が一定であれ
ば水素イオン濃度(PH)は低い程電気伝導度は上昇す
る関係を示している。
As is clear from the figure, if the mirabilite concentration and liquid temperature are constant, the lower the hydrogen ion concentration (PH), the higher the electrical conductivity.

以上のような関係から鍍金浴液中の電気伝導度と温度と
水素イオン濃度の関係は下記(1)式となり、関数補正
を行い(2)式を得る。
From the above relationship, the relationship between the electrical conductivity, temperature, and hydrogen ion concentration in the plating bath liquid is expressed by the following equation (1), and the function correction is performed to obtain equation (2).

f(λ、T、K)−M・・・・・・・・・(1)・・・
・・・・・・(2) ここで、λ:電気伝導度(μU/Cr) T:浴液温度(C) K:水素イオン濃度(PH値) M:芒硝濃度(i/7) ※A(T、K)、B(T、K)は液温とPHによる関数
補正、αは係数 この関係から浴液中の電気伝導度と、液温度とPH値を
測定して芒硝供給量を下記式により求める。
f (λ, T, K) - M (1)
......(2) Here, λ: Electrical conductivity (μU/Cr) T: Bath liquid temperature (C) K: Hydrogen ion concentration (PH value) M: Glauber's salt concentration (i/7) *A (T, K), B (T, K) are function corrections based on liquid temperature and PH, α is a coefficient From this relationship, measure the electrical conductivity in the bath liquid, liquid temperature and PH value, and calculate the supply amount of mirabilite as follows: Obtained by the formula.

ここで、λR:実測電気伝導度(μU/cl)KR:実
測水素イオン濃度(PH値) TR:実測液温度(C) Ml:測定時の芒硝濃度(E/l) λC:目標電気伝導度(μU/Cr) Mc:補正後必要芒硝濃度(9/l) ■=鍍金槽液量(m3) m:芒硝供給タンク内芒硝濃度(E/l)vm:芒硝供
給液必要量(mJ) まず上記(3)式により現状(測定時)の芒硝濃度MR
を求め次に目標の電気伝導度に上げるに必要な芒硝濃度
Mcを求める。
Here, λR: Actual electrical conductivity (μU/cl) KR: Actual hydrogen ion concentration (PH value) TR: Actual liquid temperature (C) Ml: Glauber's salt concentration at the time of measurement (E/l) λC: Target electrical conductivity (μU/Cr) Mc: Required concentration of mirabilite after correction (9/l) ■ = Volume of plating tank liquid (m3) m: Concentration of mirabilite in the mirabilite supply tank (E/l) vm: Required amount of mirabilite supply liquid (mJ) First According to the above formula (3), the current (at the time of measurement) mirabilite concentration MR
Then, find the mirabilite concentration Mc required to raise the electrical conductivity to the target value.

求めたMRとMcから上記(5)式により芒硝供給必要
量Vmを求め供給添加するものである。
From the determined MR and Mc, the required amount Vm of mirabilite to be supplied is determined by the above equation (5), and the amount is added.

第7図はこの発明制御方法の一実施例を示す図である。FIG. 7 is a diagram showing an embodiment of the control method of the present invention.

1は鍍金槽であり槽中には硫酸亜鉛の浴液が満され亜鉛
電極がセットされている。
Reference numeral 1 denotes a plating tank, which is filled with a zinc sulfate bath solution and has a zinc electrode set therein.

この夜中を鋼板2が通過し亜鉛が鍍金される。The steel plate 2 passes through this night and is plated with zinc.

このような鍍金槽においてこの発明制御方法はまず槽浴
液をポンプ3により吸引採取し電気伝導度計4と水素イ
オン濃度計(PH計)5に送られ液中の電気伝導度とP
H値が測定されたのち液は槽1に戻される。
In such a plating tank, the control method of the present invention is to first collect the tank bath liquid by suction with a pump 3 and send it to an electrical conductivity meter 4 and a hydrogen ion concentration meter (PH meter) 5 to measure the electrical conductivity and P of the liquid.
After the H value is measured, the liquid is returned to tank 1.

浴液温度は液温度検出点6より浴液温度を測定し、これ
ら測定値は演算器7へ送られる。
The bath liquid temperature is measured from a liquid temperature detection point 6, and these measured values are sent to a calculator 7.

一方芒硝供給タンク8の芒硝濃度を測定した値も演算器
7へ送られ、演算器7はこれらの測定値から前記(3)
式、(4)式、(5)式により芒硝供給必要量を算定し
コントローラ9により制研弁10によりON。
On the other hand, the measured value of the mirabilite concentration in the mirabilite supply tank 8 is also sent to the computing unit 7, and the computing unit 7 calculates the above-mentioned (3) from these measured values.
Calculate the required amount of mirabilite supply using the formulas, (4) and (5), and turn on the control valve 10 using the controller 9.

OFF制御により供給管11より槽に供給されるもので
ある。
It is supplied to the tank from the supply pipe 11 under OFF control.

12はタイマーであって、このような制御を隔時間毎に
繰返し行い目標の電気伝導度に保持するものである。
Reference numeral 12 denotes a timer that repeatedly performs such control every other hour to maintain the target electrical conductivity.

この発明制御方法を月産能力12400T/Mの亜鉛鍍
金工場に実施した。
This invention control method was implemented in a zinc plating factory with a monthly production capacity of 12,400 T/M.

浴液の温度はあまり高いとヒユームの問題を考慮して最
大70℃とし、電気伝導度の目標を128X103μU
/1mとして実施した結果、従来芒硝濃度平均50&/
L、電気伝導度108X103μU/cIのものが、芒
硝濃度100&/L、電気伝導度128X103μU/
77に増加することができ消費電力は製品基当り12K
WHの電力が節約でき、鋼板の品質も向上した。
The temperature of the bath liquid is set at a maximum of 70°C to avoid the problem of fume if it is too high, and the target electrical conductivity is set at 128 x 103 μU.
/1m, the average concentration of mirabilite was 50 &/
L, electrical conductivity 108 x 103 μU/cI, mirabilite concentration 100 &/L, electrical conductivity 128 x 103 μU/cI.
77 can be increased to 12K power consumption per product base
The power consumption of the WH was saved, and the quality of the steel sheet improved.

【図面の簡単な説明】 第1図、第2図、第3図は浴液中の芒硝濃度、温度、水
素イオン濃度(PH)により夜中の電気伝導度が変化す
る状態を示す図、第4図は芒硝濃度と電気伝導度の関係
を示す図、第5図はPH値2.5のときの芒硝各濃度に
おける液温度と電気伝導度の関係を示す図、第6図は浴
液の水素イオン濃度(PH値)と電気伝導度の関係を示
す図、第7図はこの発明制御方法の一実施例を示す図で
ある。 1・・・・・・鍍金槽、2・・・・・・鋼板、3・・・
・・・ポンプ、4・・・・・・電気伝導度計、5・・・
・・・水素イオン濃度計、6・・・・・・液温度検出点
、7・・・・・・演算器、8・・・・・・芒硝供給タン
ク、9・・・・・・コントローラ、10・・・・・・制
御弁、11・・・・・・供給管、12・・・・・・タイ
マー。
[Brief explanation of the drawings] Figures 1, 2, and 3 are diagrams showing how the electrical conductivity changes during the night depending on the concentration of mirabilite, temperature, and hydrogen ion concentration (PH) in the bath liquid. The figure shows the relationship between the concentration of Glauber's salt and electrical conductivity. Figure 5 shows the relationship between the liquid temperature and electrical conductivity at each concentration of Glauber's salt when the pH value is 2.5. Figure 6 shows the relationship between hydrogen in the bath solution. FIG. 7 is a diagram showing the relationship between ion concentration (PH value) and electrical conductivity, and is a diagram showing an embodiment of the control method of the present invention. 1...Plating tank, 2...Steel plate, 3...
...Pump, 4...Electric conductivity meter, 5...
... Hydrogen ion concentration meter, 6 ... Liquid temperature detection point, 7 ... Arithmetic unit, 8 ... Glauber's salt supply tank, 9 ... Controller, 10... Control valve, 11... Supply pipe, 12... Timer.

Claims (1)

【特許請求の範囲】 1 電気鍍金浴中の電気伝導度と浴液温度および水素イ
オン濃度を測定し、これらの測定値から電気伝導度調整
剤である芒硝濃度を下記式により制御することを特徴と
する電気鍍金浴の電気伝導度制御方法。 ここで、M:芒硝濃度(g/l) λ:電気伝導度(μU/Cr) T:浴液温度(C) K:水素イオン濃度(P(値) ※A(T、K)、B(T、K)は液温とPHによる関係
補正、αは係数
[Claims] 1. The electrical conductivity, bath liquid temperature, and hydrogen ion concentration in the electroplating bath are measured, and the concentration of Glauber's salt, which is an electrical conductivity regulator, is controlled using the following formula from these measured values. A method for controlling the electrical conductivity of an electroplating bath. Here, M: Glauber's salt concentration (g/l) λ: Electrical conductivity (μU/Cr) T: Bath temperature (C) K: Hydrogen ion concentration (P (value) *A (T, K), B ( T, K) are relationship corrections based on liquid temperature and PH, α is the coefficient
JP55138581A 1980-10-02 1980-10-02 Method for controlling electrical conductivity of electroplating bath Expired JPS5810480B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55138581A JPS5810480B2 (en) 1980-10-02 1980-10-02 Method for controlling electrical conductivity of electroplating bath

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55138581A JPS5810480B2 (en) 1980-10-02 1980-10-02 Method for controlling electrical conductivity of electroplating bath

Publications (2)

Publication Number Publication Date
JPS5763699A JPS5763699A (en) 1982-04-17
JPS5810480B2 true JPS5810480B2 (en) 1983-02-25

Family

ID=15225457

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55138581A Expired JPS5810480B2 (en) 1980-10-02 1980-10-02 Method for controlling electrical conductivity of electroplating bath

Country Status (1)

Country Link
JP (1) JPS5810480B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2712661B2 (en) * 1989-11-15 1998-02-16 住友金属工業株式会社 How to adjust the electroplating bath
KR100846341B1 (en) 2007-09-27 2008-07-15 대륙금속(주) Trivalent chromium abstinence control device

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4860029A (en) * 1971-12-03 1973-08-23
JPS5324897B2 (en) * 1972-09-27 1978-07-24
JPS5230937B2 (en) * 1972-09-27 1977-08-11
JPS51149132A (en) * 1975-06-17 1976-12-21 Nippon Kokan Kk Method of controlling concentration of acid tin electroplating bath

Also Published As

Publication number Publication date
JPS5763699A (en) 1982-04-17

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