• Proceedings of the Korean Institute of Resources Recycling Conference
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• 2005.05a
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• pp.23-27
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• 2005

Electrogenerated chlorine leaching of used printed circuit board was Investigated in hydrochloric acid solution. The used printed circuit board contained about 45% of metal component, in which copper was about 84%. The leaching rate was greatly effected by current density and agitation. Utilization of electrogenerated chlorine was enhanced by increasing agitation and lowering current density. Leaching of copper was suppressed, while the minor metal elements, such as aluminum, lead, and tin, dominated the leaching at the initial stage.

• Resources Recycling
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• v.22 no.6
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• pp.55-63
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• 2013

In this study, a electrochemical-chemical combined dissolution technology was conducted by electro-generated chlorine to obtain ruthenium solution from ruthenium metal. To find out the optimum leaching conditions of ruthenium in chloride solution, this leaching process was carried out on the variation of pH, reaction time, temperature and applied voltage at the electro-generated chlorine system in the reaction bath. Also, ozone generator was used to obtain ruthenium(III) chloride solution to increase the leaching rate. The optimum condition was observed at pH 10.0, $40^{\circ}C$ within 1 hr of reaction time that more than 88% of ruthenium(III) chloride dissolved.

• Proceedings of the Korean Institute of Resources Recycling Conference
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• 2006.05a
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• pp.86-89
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• 2006

전해 생성된 염소를 이용하여 구리를 침출하는 연구를 수행하였다. 염산농도 $1molL^{-1}$, 반응온도 $25^{\circ}C$, 교반속도 400rpm 조건에서 전류밀도 $10mA/cm^{2}$의 경우 반응온도에 상관없이 구리의 침출속도가 동일하였으나 $Cl_{2}$ 생성량이 충분한 $40mA/cm^{2}$의 경우 온도가 높을수록 구리의 침출속도가 증가하였다. 침출된 구리농도가 6g/L 부근에 도달하면 염소의 공급속도에 상관없이 구리의 침출이 둔화되었다. 이는 구리-염소 착화물의 형성과 관련된 것으로 생각된다.

• Journal of the Korean Applied Science and Technology
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• v.29 no.4
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• pp.570-576
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• 2012

In this study, we investigated the characteristics of NO oxidation using un-divided electrolyzed seawater as oxidant. The concentration of available chlorine and the temperature of electrolyzed seawater are increased with electrolysis time in the closed-loop constant current electrolysis system. While NO gas flow through bubbling reactor which is filled with electrolyzed seawater, the oxidation rate of NO to $NO_2$ is increased with the concentration of available chlorine and the temperature. $NO_2$, generated by oxidation reaction, is dissolved in electrolyzed seawater and existed as $HNO_3{^-}$ ion.

• Resources Recycling
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• v.17 no.6
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• pp.24-33
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• 2008

The leaching of Cu from waste PCBs was investigated with electro-generated chlorine as an oxidant. The leaching experiments were carried out according to the design of experiments to analyze quantitatively the effect of parameters on copper leaching. From the analysis of variance (ANOVA) it was suggested that the effective parameters were current density, temperature, concentration of HCl, and the interaction between the concentration of HCl and temperature. Especially, the effect of current density was analyzed to contribute to the interpretation of result for copper leaching up to 95.7%. A multiple regression model obtained from the analysis of effective parameters explained 99% of leaching results. From the model equation, it was found that the effect of HCl concentration on copper leaching increased with temperature.

• Resources Recycling
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• v.14 no.5 s.67
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• pp.45-53
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• 2005

Electro-generated chlorine leaching of waste printed circuit boards was investigated in hydrochloric acid solutions. Non-magnetic component of $0.6{\sim}1.2mm$ was prepared by grinding, magnetic separation, and sieving. The non-magnetic component of pulverized printed circuit board contained about 45% of metal component, in which copper was about 83.6%. The leaching rate of copper was greatly affected by current density and agitation speed. The leaching of copper up to 98% was achieved at $20mA/cm^2$, $50^{\circ}C$, 180 minutes, and 600 rpm in 1M HCl solutions. Increasing agitation and lowering current density enhanced utilization efficiency of electro-generated chlorine. Leaching of copper was suppressed at the initial stage, while the minor metal elements, such as aluminum, lead, and tin, were dominantly leached out.

• Journal of Korean Society of Environmental Engineers
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• v.31 no.8
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• pp.627-634
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• 2009

This study was done to find out the formation mechanism of chlorate by electrochemical process using chloride ion ($Cl^-$) as an electrolyte. Firstly, the effective factors such as pH and initial chloride concentration were figured out to see the formation property of chlorate during electrolysis. And the relation of free chlorine, and mixed oxidants such as OH radical and ozone with chlorate were estimated to concretize the formation mechanism. As a result, it was found that the major reaction of chlorate formation would be electrochemical reaction with free chlorine, and also the direct oxidation of chloride ion and the reaction by OH radical were participated in the formation of chlorate. Moreover, it was observed that formed chlorate was oxidized to perchlorate. Lastly, the optimum condition was recommended by comparing free chlorine with chlorate concentration during the electrochemical process with the different electrode separation.

• Resources Recycling
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• v.15 no.6 s.74
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• pp.33-40
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• 2006

Leaching behavior of copper using electro-generated chlorine was investigated in hydrochloric acid solutions. When leached copper concentration was lower than 3.6g/L, the utilization efficiency of the electro-generated chlorine was close to 100% at $10mA/cm^2,\;25^{\circ}C$, 400 rpm in 1M HCl solutions. The concentration ot the leached copper over 3.6g/L caused the electrode potential to drop quietly, leading to a change or leaching mechanism. The leaching rate oi copper began to decrease at the concentration of copper 5.2g/L. This is probably due to the formation of a layer of CuCl on Cu metal in 1M HCl solutions. The leaching rate, however, was not retarded in a solution ot high chloride concentration. The high solubility of CuCl in the solution may prevent the formation of CuCl on Cu metal.

• Clean Technology
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• v.18 no.4
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• pp.446-450
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• 2012

Strong alkaline electrolyzed water which is produced in cathode by electrolyzing the solution where electrolytes (NaCl, $K_2CO_3$ etc.) are added in diaphragm electrolytic cell, is eco-friendly and has cleaning effects. So, it is viewed as a substitution of chemical cleaner. In addition, strong alkaline electrolyzed water is being used by some Japanese automobile and precision parts manufacturing industries. When strong alkaline electrolyzed water is produced by using diaphragm electrolytic cell, it is necessarily produced at the anode side. Since strong acidic electrolyzed water produced is discarded when its utilization cannot be found, production efficiency of electrolyzed water is consequently decreased. Also, there is a weakness electrolytic efficiency is decreasing due to the pollution of diaphragm. In order to overcome this, non-diaphragm all-in-one electrolytic cell integrated with electrode reaction chamber and dilution chamber was applied. Strong alkaline electrolyzed water was produced for different composition of electrolytes, and their properties and characteristics were identified. In comparing the properties between strong alkaline electrolyzed water produced in diaphragm electrolytic cell and that produced in all-in-one electrolytic cell, the differences in ORP and chlorine concentration were found. In emulsification test to confirm surface-active capability, similar results were obtained and strong alkaline electrolyzed water produced in non-diaphragm all-in-one electrolytic cell was identified to be useable as a cleaner like strong alkaline electrolyzed water produced in diaphragm electrolytic cell. Strong alkaline electrolyzed water produced in non-diaphragm all-in-one electrolytic cell is thought to have sterilizing power because it has active chlorine which is different from strong alkaline electrolyzed water produced in diaphragm electrolytic cell.

• Nuclear Engineering and Technology
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• v.29 no.6
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• pp.60-64
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• 1997

핵연료의 가공공정에서 발생하는 스러지를 건식처리공정으로 회수 정제할 수 있는 건식처리 방법에 대하여 논의하고자 하였다. 건식처리방법은 수용액을 전혀 사용하지 알기 때문에 폐기물의 발생량이 습식처리방법에 비해 훨씬 줄어든다. 산화우라늄은 고온의 용융염중에서 염소개스에 의해 염소화반응을 통하여 우라늄염화물을 생성되게 되어 이들은 전기적으로 이동이 가능한 형태로 바뀌므로 전극에 선택적으로 전착될 수 있기 때문에 다른 금속이온과 분리할 수 있다. 본 보고서에서는 산화우라늄의 염소화공정, 전착공정에 대하여 기술하였고 전착된 산화물의 물리적 특성에 대하여 요약하였다.