• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2001.09a
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• pp.191-194
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• 2001

The electrokinetic apparatus for remediation of the soil contaminated with Cs$^{+}$was designed. After kaolin clay was compulsorily contaminated by Cs$^{+}$ solution, the remediation characteristics by electrokinetic method were analyzed. After remediation experiment, the pH of the cathode side of the soil column was increased to 12.7 due to the generation of OH in cathode reservoir, but no hydroxide cesium form in the cathode side. Effluent rate from the cathode almost was constant and cesium concentration of effluent decreased with time passage. The 49% of a total of Cs$^{+}$ in the column was decontaminated for 0.4 day, the 72% of a total of Cs$^{+}$ in the column was decontaminated for 0.8 day, the 83% of a total of Cs$^{+}$ in the column was decontaminated for 1.2 days, the 89% of a total of Cs$^{+}$ in the column was decontaminated for 1.6 days, and the 93% of a total of Cs$^{+}$ in the column was decontaminated for 2.1 day Meanwhile, the predicted values of residual concentration by the developed model were quite similar to those obtained from experiments.m experiments.

• Journal of Soil and Groundwater Environment
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• v.7 no.3
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• pp.85-94
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• 2002

Overall objective of this study was to evaluate the electrochemical characteristics of fine soils during the electrokinetic(EK) remediation. Zeta potential of kaolinite as a function of solution pH and surfactant concentration was investigated to make a relationship with electroosmotic flow direction and rate. During the EK experiments, pH of pore solution, electroosmotic permeability($k_e$), electric conductivity($\delta_e$) and voltage distribution was measured, respectively, The point of zero charge(PZC) of kaolinite was estimated to be about 4.2 and the zeta potential of kaolinite above PZC was more negative as solution pH increased. Sorption of surfactants on the kaolinite altered the zeta potential of kaolinite. resulting from the variation of electrochemical characteristics of kaolinite surface. hs the EK experiment progressed, low pH was predominant over most of the kaolinite specimen and thus resulted in very low mass and charge flow. The $k_e$ and $\delta_e$ was also affected by the variation of voltage drop across the EK column with time. Results from this study implied that zeta potential of kaolinite affected by the pH variation of pore solution and voltage distribution in soil column played important role in the determination of mass and charge flow during EK process. It was also suggested that pH adjustment or addition of suitable sorbates could alter the electrochemical characteristics of soil surface and thus maintain high mass and charge flow rate with time.

• Analytical Science and Technology
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• v.9 no.1
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• pp.35-42
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• 1996

A rapid analytical method based on capillary electrophoresis is described for the determination of trace anions in high-purity chemicals which is used to prevent corrosion demage in nuclear power plants. Separations are carried out at 20kV using trimethylsilane-coated fused-silica capillary ($70cm{\times}50$ or $75{\mu}m$ i.d.) with the electrolyte of 5mM Chromate(pH=8). Detection was achieved using on-column indirect photometry at 254nm. The simultaneous analysis of inorganic anions, chloride, nitrate, sulfate, azide and phosphate was performed using methods of hydrodynamic(>1ppm) and / or electrokinetic(<1ppm) injection. The results of studies on the coexisting anions on analyte ions shows that peak responses of analyte in hydrodynamic injection is constant without effect of coexisting anions, but those of analysis in electrokinetic injection is strongly dependant upon the kind of coexisting anions and its ionic mobility. The analyte enrichment rate, hence peak response, is positive relationship with the resistance of the sample solution. Thus, appropriate measures, such as standard addition or internal standard technique, must be used to account for differences in conductance of standard and sample solutions.

• Journal of Environmental Science International
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• v.13 no.1
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• pp.61-68
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• 2004

Three kinds of toxic heavy metals, such as lead, copper, and cadmium, existing abundantly in contaminated soils were selected to investigate pH change, electroosmotic flow, and the removal rate in the application of electrokinetic process. In the change of pHs, they reached to about 12 and 2 at each cathodic and anodic region, respectively, and maintained for reaction being proceeded. Electroosmotic flow rates were not influenced by the kind of metal species but by electropotential gradient. On the soils contaminated by each metal, the removal rate of Cd was the fastest among three as in the order of Cd>Pb>Cu. While on the soils contaminated by mixed metal species, Cu was the fastest. Metal species transported by electrokinetic processes were distributed in between 0.9 and 1.0 of normalized region. In the case of soils contaminated by one kind of metal. the relative concentrations of Pb and Cd estimated in between normalized region 0.9 and 1.0 were 5.2 and 5.7, respectively.