• Proceedings of the PSK Conference
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• 2003.04a
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• pp.293.1-293.1
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• 2003

Electroosmotic flux during iontophoresis originates due to the net negative charge of the current passing channels (pores) in skin at physiological pH (pH 7.4). Thus, the channels are permselective to cations, and this causes the convective solvent flow from anode to cathodal direction. This solvent flow facilitates the flux of cations (from anode), inhibits that of anions (from cathode), and enables theenhanced transport of neutral, polar solutes. (omitted)

• Journal of Soil and Groundwater Environment
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• v.18 no.1
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• pp.129-136
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• 2013

This research was conducted to investigate effects of acid buffering capacity and soil component in treatment of phenanthrene using electrokinetic-Fenton process. In Hadong clay of high acid buffering and low iron oxide content, it was difficult to oxidize phenanthrene due to shortage of iron catalyst and scavenger effect of carbonate minerals. The desorbed phenanthrene conductive to Fenton oxidation was transported toward cathode by electroosmotic flow. However, in Youngdong illitic clay, oxidation of phenanthrene near anode readily occurred compared to Hadong clay due to high iron content and low acid buffering capacity.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.04a
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• pp.31-34
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• 2004

Feasibility of electrokinetic(EK)-Fenton process and Ozone chemical oxidation were investigated for tile removal of organic contaminants and heavy metals from the contaminated soil. In EK-Fenton process, accumulated electroosmotic flow(EOF) was 80 L for 26 days. Removal efficiency of TPH, As, and Ni were 61%, 36%, and 47%, respectively. The concentration of As was high near the anode due to the transport of anionic As toward the anode, while the concentration of Ni was high near the cathode by the movement of cationic Ni to the cathode. Field scale application of in-situ ozonation was carried out for removal of TPH in 3-D test cell (3 m$\times$2 m$\times$2 m). After 25 days of ozone injection, more than 80% of removal rate was observed through the test cell.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.04a
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• pp.346-349
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• 2004

Surfactant-enhanced electrokinetic (EK) process was investigated to remove polycyclic aromatic hydrocarbons (PAHs) from low-permeable soils. Phenanthrene and kaolinite were selected as a representative PAH and a model soil, respectively. A nonionic surfactant Tergitol 15-S-12 was applied to improve the solubility of phenanthrene and sodium chloride was used as an electrolyte at the various concentrations from 0.001 to 0.1M. The addition of electrolyte affected both the removal efficiency and operation cost. When electrolyte was introduced, the electrical potential gradient became low and thus power consumption was reduced. However, as electrolyte concentration increased, the electroosmotic flow also decreased, so the removal efficiency of contaminant decreased. Therefore, the removal efficiency and power consumption should be considered simultaneously to determine the iptimum surfactant concentration, so a relatively lower concentration of electrolyte than certain value is desired.

• 유체기계공업학회:학술대회논문집
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• 2006.08a
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• pp.171-174
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• 2006

When two particles close to each other are in electrophoretic motion, each particle is under the influence of the non-uniform electric field generated by the other particle. Two particles may attract or repel each other due to the dielectric force depending on their positions in the non-uniform electric field. It is shown analytically that two adjusting rigid particles can form an aggregate due to the dielectric interaction. To verify the validity of the theoretical prediction, an experiment is carried out by using a microchannel. In the experiment, AC electric field is used to eliminate cumbersome electroosmotic flow. The experimental result shows that the particles form a chain-like structure, which is typically observed in electro-rheological fluid, due to the dielectric interaction.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2003.09a
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• pp.356-359
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• 2003

Polycyclic aromatic hydrocarbons (PAHs) are representative hydrophobic organic carbons (HOCs). Surfactant-enhanced electrokinetic (EK) remediation is an innovative in-situ technology that can effectively remove HOCs from low-permeability soils. In this study, the electrokinetic remediation using Tergitol 15-S-12, a nonionic surfactant, was conducted for the removal of phenanthrene from kaolinite. Tergitol 15-S-12 was used at concentrations of 1.5, 2.0, 2.5 and 7.5 g/L to enhance the solubility of phenanthrene. When the surfactant solution was applied to EK system, high electrical potential gradient was maintained and the amount of electroosmotic flow decreased. Removal efficiency of phenanthrene was proportional to the concentration of Tergitol 15-S-12 because the solubility and mobility of phenanthrene was enhanced by surfactant micelle. Therefore, the suitable concentration of nonionic surfactant Tergitol 15-S-12 is expected to improve the removal efficiency of PAHs in EK remediation.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2003.09a
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• pp.158-161
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• 2003

Removal of phenanthrene by electrokinetic method combined with Fenton-like process was studied in a model system. The scale of reactor was 100cm in length, 100cm in width, and 70cm in height. The distance between electrodes was 70cm. Indonesia kaoline was selected as a model soil. When constant voltage of 100 V was applied to this system, current decreased from 200 mA to 100 mA for 14 days. Total accumulated EOF was about 55,000 mL. The concentration of phenanthrene near anode was very low because direction of electroosmosis was from anode to cathode and hydrogen peroxide was supplied to anode reservoir. Phenanthrene concentration was increased as the location was far from anode because hydrogen peroxide was gradually decomposed and then the rate of hydroxyl radical production was decreased.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.09a
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• pp.239-242
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• 2002

Removal of phenanthrene by electrokinetic (EK) method combined with Fenton-like process was studied in a model system. Sand and phenanthrene were selected as a model soil and a representative PAH. Sand was contaminated at the concentration of 500 mg phenanthrene/kg dry sand. Bentonite and kaolinite were inserted into the space between reservoir and contaminated soil. When hydrogen peroxide supplied to a soil system from the anode reservoir was transported through the soil by EK process, the Fenton-like reaction was occurred by naturally existing iron minerals in soil. When hydrogen peroxide was supplied into the system, it showed higher removal efficiency than when just water was used. Maximum removal efficiency of phenanthrene was 81.2 % for 7 days.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2003.04a
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• pp.306-309
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• 2003

Surfactant-enhanced electrokinetic (EK) remediation is an emerging technology that can effectively remove hydrocarbons from low-permeability soils. In this study, the electrokinetic remediation using Calfax 16L-35 was conducted for the removal of phenanthrene from kaolinite. An anionic surfactant Calfax 16L-35 was used at concentrations of 5, 15, and 30g/L to enhance the solubility of phenanthrene. When the surfactant solution was applied to EK system, low electrical potential gradient was maintained because of its ions. Even when the surfactant concentration was high, the removal efficiency of phenanthrene was low After the operation, most of surfactants were remained in soil and there were few in effluent. This phenomena was observed because the migration of Calfax 16L-35 from cathode to anode was predominant over electroosmotic flow which moved in opposite direction. Therefore, the anionic surfactant Calfax 16L-35 is considered to be improper in surfactant - enhanced electrokinetic remediation.

• Bulletin of the Korean Chemical Society
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• v.20 no.12
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• pp.1483-1486
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• 1999

The contents of pentachlorophenol (PCP) and 2,3,5,6-tetrachlorophenol (TeCP) in textile products are regulated for safety. Since an organic solvent such as 2-methoxyethanol is needed to extract chlorinated phenols from textile samples, nonaqueous capillary electrophoresis has been applied to achieve the separation of PCP and isomers of TeCP. The run buffer was 100 mM Tris/acetate in methanol whose pH was adjusted to 8.0. All of the analytes were negatively charged at pH 8.0 and their electrophoretic velocities were higher than the electroosmotic flow of the methanol buffer. A reverse voltage of -20 kV was applied along a 27-cm fused silica capillary with ID of 50 μm, and PCP and 3 TeCP isomers were separated based on the difference in $pK_a$ values in less than 4 min. The limits of detection (S/N = 3) were about 0.02 μM. By varying pH of the methanol run buffer, $pK_a$ values of the 4 chlorinated phenols were also estimated.