• Journal of the Korean Society of Industry Convergence
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• v.19 no.4
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• pp.176-184
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• 2016

Electrochemical ion exchange method is expected to be one of the most acceptable techniques for the separation of radioactive cations from nuclear wastewater. In this study a thin film of hexacyanoferrate on nickel surface was derivatized chemically in an aqueous potassium-ferricyanide solution. Electrochemical redox behavior of the nickel hexacyanoferrate(NiHCNFe) film electrode was investigated with the use of cyclic voltammetry potentiostated from -100 to 800 mV versus SCE. The electro-reduction characteristics of the NiHCNFe film were examined in the cobalt solutions. The NiHCNFe ion exchanger was more useful at lower concentration, lower temperature, and pH7 of the cobalt solution. The capacity loss of NiHCNFe was 0.018%/cycle that was less than the average loss of 2~3%/cycle of the convective organic exchanger. The 45~55% of the initial cobalt ions was electro-deposited on the NiHCNFe by using continuous recirculating reactor system. As a result, it was found that the electroactive NiHCNFe films showed better performance than the organic resins for the separation of cobalt ion from the aqueous solutions.

• Journal of the Korean Chemical Society
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• v.28 no.3
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• pp.176-184
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• 1984

Retention behavior of benzoic acid and its derivatives on XAD-2 in the alcoholic aqueous solution was investigated and separation was attempted. Retention was affected by the concentration and kinds of added organic solvents, the pH of the aqueous solution, the added $R_4N^+$ and the position and kinds of functional group in the sample molecules. Retention of sample acids in acidic conditions was due to mainly molecular adsorption on nonpolar XAD-2 surface and that in basic conditions was due to mainly ion-pair model. In these bases a mixed sample was separated in EtOH 20% aqueous solution at pH 8.50.

• Journal of Korean Society of Water and Wastewater
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• v.20 no.3
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• pp.389-395
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• 2006

The use of pine bark, a natural adsorbent prepared from Korean Red Pine (Pinus densifloral), was studied for its adsorption behavior of lead ion from aqueous solution. Adsorption experiments were carried out on lead ion concentrations of 10mg/L. Adsorption of lead ion could be described by both Langmuir and Freundlich adsorption isotherms. Treatment of the bark with nitric acid greatly increased initial adsorption rate, and equilibrium sorption capacity increased by approximately 48%. A pseudo second-order kinetic model fitted well for the kinetic behavior of lead ion adsorption onto the bark. Acid-treated bark demonstrated its adsorption capacity quite close to that of granular activated carbon. Results of this study indicated that ion exchange and chelation were involved in the adsorption process.

• Proceedings of the Membrane Society of Korea Conference
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• 1994.04a
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• pp.55-56
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• 1994

There has been many attempts to improve the membrane performance using pervaporation processes[l-3]. They are 1) blending polymer with the high flux and one with high selectivity, 2) an incorporation of functional groups interacting with permeants into a membrane through copolymerization or modification, 3) composite membrane or asymmetric membrane structure with a thin skin layer which acts as a selective layer. Among them, a polymeric membrane containing ion complex group receives an extensive attention recently because ionic complex is known to activate the water transport through ion-dipole interaction. It is especially advantageous in the separation of organic-water system. We applied the ideas of the activation of water transport through ion-dipole. We have reported on the in-sire complex membrane to separate water from aqueous aceiic acid and pyridme solution[4-5] based on the simple acid-base theory. Water transport was enhanced through in-situ complex between pyridine moiety in the membrane and the incoming acetic acid in the feed. In this case, catalytic transport mechanism was proposed. In the present study we used pyridine solution as a feed and the sulfonic acid group in the membrane.

• Journal of the Korean Chemical Society
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• v.17 no.6
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• pp.416-423
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• 1973

Formation of the complexes of alkaline earth metal ions with malonate and o-phthalate ions in aqueous, ethanol-water and acetone-water solutions (20% by volume) was studied at room temperature by the equilibrium ion exchange technique. This technique involved the measurements of distribution of radioactivity between cation exchange resin(Ion Exchange Resin CGC 241) and solution phases after the radioactive metal ions were equilibriated with the cation exchange resin in the presence of malonate or o-phthalate ions of varying concentrations. The pH of the solutions was controlled to 7.2~7.5, and the ionic strength of the solutions was kept at 0.10~0.11. The results of the present study indicated that the alkaline earth metal ions formed one-to-one complexes with the dibasic organic acids in all solvent systems examined. The present study showed that the relative stabilities of the complexes increased in the order: $Ba^{++}\;<\;Sr^{++}\;<\;Ca^{++}$ complexes. It was also observed that the relative tendency of the o-phthalate ion for the complex formation was somewhat greater than that of malonate ion in each solvent system. Furthermore, it was noted that the complexes were formed more readily in the mixed solvent than in the aqueous solution.

• Textile Coloration and Finishing
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• v.15 no.3
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• pp.146-153
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• 2003

This article describes the metal ions adsorption of chitosan fibers. The chitosan fibers were manufactured by wet spinning using 2% acetic acid as solvent, 10% aqueous sodium hydroxide as non solvent, and 4%chitosan solution as a solvent. The adsorption characteristics of chitosan fibers towards 100ppm solutions of various metal ions such as Cu(II), Cd(II), Cr(III), Hg(II) were examined at different pH value by ICP-Atomic Emission Spectrometer. The adhesiveness of metallic ions to the chitosan fiber were increased with the increase of pH and the decrease of denier. On the other hand, from pH4, chitosan fiber that is immersed in metal ion aqueous solution of Cu(II) and Cd(II) became homogeneous solution because is dissolved. The adhesiveness of metallic ions to chitosan fiber were found to increased in a sequence of Hg(II)> Cr(III)> Cu(II)> Cd(II). The antimicrobial characteristics of the chitosan fiber by adhered metal ions, virgin chitosan fiber, and cotton fiber were evaluated. The antimicrobial activity of the fibers were increased with the decrease of denier.

• Bulletin of the Korean Chemical Society
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• v.18 no.3
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• pp.287-291
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• 1997

The photochemical reaction of aqueous dichloromethane in the absence (saturated with argon) and the presence of O2 (saturated with air or oxygen) has been investigated using 184.9 nm UV light. The irradiation of the solution causes the formation of 1,2-dichloroethane, 1,1,2-trichloroethane, 1,1,2,2-tetrachloroethane and chloride ion. The initial quantum yield of the products in the absence of oxygen was determined to be 8.6 × 10-3, 7.3 × 10-3, 4.4 × 10-3 and 2.3 × 10-2, respectively. In addition to these main products, small amounts of 1,2,3-trichloropropane, 1,1,2,2,3-pentachloropropane, 1,1,2,3,3-pentachloropropane, 1,3-dichloropropane and 1,1,2,2,3,3-hexachloropropane were detected. In the presence of oxygen, hydrogen peroxide was also detected along with the products listed above. With increasing the concentration of oxygen, while formation of the chlorinated organic products diminished, formation of chloride ion increased. Probable reaction mechanisms for the photochemical reaction were presented on the basis of products analysis.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 2003.11a
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• pp.103-108
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• 2003

A method to determine chromium(III) ion in aqueous solution by chemiluminescence method using a lucigenin entrapped silica sol-gel film has been studied. An optical probe for chromium(III) ion has been prepared by entrapping lucigenin into silica sol-gel film coated on a glass support by dip coating. The chromium(III) optical sensor is based on the catalytic effect of chromium(IIII) ion on the reaction between lucigenin and hydrogen peroxide in basic solutions. The effects of Nafion, DMF and Triton X-100 were investigated to find the optimum condition to minimize cracking and leaching from the probe. The effects of pH and concentrations of lucigenin and hydrogen peroxide on the chemiluminescence intensity were investigated. The chemiluminescence intensity was increased linearly with increasing chromium(III) concentration from $2.5{\times}10^{-4}$M to $8.0{\times}10^{-7}$M and the detection limit was $4.0{\times}10^{-7}$M.

• Journal of Environmental Science International
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• v.11 no.4
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• pp.361-366
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• 2002

Several effects on Pb$^{2+}$ removal by crab shell from aqueous solution were investigated. As the increase of initial Pb$^{2+}$ concentration and decrease of initial crab shell concentration, the time required to reach an equilibrium state and the residual Pb$^{2+}$ concentration increased. In our experimental ranges, the optimum initial Pb$^{2+}$ concentration and crab shell concentration were below 103 mg/$\ell$ and over 0.5 mg/$\ell$, respectively. Also, in order to investigate the mechanism of Pb$^{2+}$ removal by crab shell in aqueous solution, the crab shell was compared with chitosan and chitin on aspects of Pb$^{2+}$ removal capacity and Pb$^{2+}$ removal rate. The Pb$^{2+}$ removal by crab shell was greater than that by chitin and chitosan. The role of chitin was not so great in Pb$^{2+}$ removal by crab shell. The Pb$^{2+}$ removal by chitosan was not exactly correlated to the molecular weight of chitosan. weight of chitosan.

• Bulletin of the Korean Chemical Society
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• v.6 no.6
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• pp.329-333
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• 1985

A procedure for the preparation of peptizable pseudoboehmite has been described in detail based upon a process of neutralization of an aqueous aluminum sulfate or chloride solution with aqueous ammonia. In order to obtain peptizable pseudoboehmite products, carefully controlled conditions were required in the whole processes of neutralization, aging, washing, and drying. The optimum conditions experimentally found are the following. The aluminum salt solution is neutralized with aqueous ammonia until the final pH of the solution reaches 10.0 to 10.8 or 9.0 to 9.3 for the sulfate of chloride, respectively. The alumina gel formed is subjected to aging at $80^{\circ}C for about 3 hours and washed with water more than 5 times to reduce the residual sulfate or chloride ion in the final products to less than 4%. The pseudoboehmite gel thus obtained should be dried oven at 80 to $100^{\circ}C for a few to several hours depending on the selected temperatures.