• Journal of the Korean Society of Industry Convergence
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• v.20 no.4
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• pp.257-263
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• 2017

The following thesis researched into the characteristics of electrolytic ion water with different levels of electrical conductivity by adding NaCl into tap water which is for experimental use in multi-layered electrolytic ion water generator. Electrolytic ion water is generated by underwater electrolysis and the electrolysis generator has a simple structure, is easy to control and is highly utilized in industries. Electrolytic ion water is useful in many areas since it has a superior sterilizing power, has no possibility of secondary pollution itself as water and removes active oxygen. In the experiment, we used tap water with NaCl excluded and water with three different levels of electrical conductivity by changing NaCl concentration levels into three levels. The features of current and voltage in electrolytic ion water represented a form of quadric instead of the linear characteristic following ohm's law. As well, as the electric conductivity of water and applied voltage increased, we were able to generate much stronger acid water and alkali water.

• Bulletin of the Korean Chemical Society
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• v.31 no.2
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• pp.303-308
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• 2010

Pseudo-first-order rate constants ($k_{obsd}$) have been measured spectrophotometrically for nucleophilic substitution reactions of 4-nitrophenyl benzoate (5a), 4-nitrophenyl 4-methoxybenzoate (5b), and 4-nitrophenyl 4-hydroxybenzoate (5c) with alkali metal ethoxides, $EtO^-M^+$ ($M^+=Li^+$, $Na^+$ and $K^+$) in anhydrous ethanol (EtOH) at $25.0{\pm}0.1^{\circ}C$. The plots of $k_{obsd}$ vs. [$EtO^-M^+$] exhibit upward curvatures in all cases, indicating that $M^+$ ions catalyze the reactions and ionpaired $EtO^-M^+$ species are more reactive than dissociated $EtO^-$. Second-order rate constants for reactions with dissociated $EtO^-$ and ion-paired $EtO^-M^+$ (i.e., $k_{EtO^-}$ and $k_{EtO^-M^+}$, respectively) have been calculated from ion-pair treatment for the reactions of 5a and 5b. However, such ion-pair treatment has failed to determine $k_{EtO^-}$ and $k_{EtO^-M^+}$ values for the reactions of 5c. It has been concluded that reactions of 5a and 5b are catalyzed by one metal ion, which increases electrophilicity of the reaction center through coordination on the carbonyl oxygen. In contrast, reactions of 5c have been suggested to involve two metal ions, i.e., the one coordinated on the carbonyl oxygen increases the electrophilicity of the reaction center while the other one associated on the phenoxy oxygen decreases the charge repulsion between the anionic reagents (i.e., $EtO^-$ and deprotonated 5c). It has been found that the rate equation derived from the mechanism involving two metal ions fits nicely to the kinetic results obtained for the reactions of 5c.

• Journal of the Korean Chemical Society
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• v.39 no.5
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• pp.371-378
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• 1995

The triazacrown compound, 1,7-dioxa-4,10,13-triazacyclopentadecane trihydrobromide salt (Na3O2-3HBr) was synthesized. And this compound was used to synthesize the new ion exchanger, which combined with Merrifield peptide resin. This new ion exchanger had a capacity of 3.2 meq/g dry resin. And the distribution coefficients of alkali and alkaline earth metal ions on this ion exchanger in the various concentrations of hydrochloric acid were determined. The ion exchange behaviors of alkali and alkaline earth metal ions in the various hydrochloric acid concentrations are, also, discussed.

• Bulletin of the Korean Chemical Society
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• v.31 no.2
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• pp.453-456
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• 2010

The structural and energetic preferences of thiacalix[4]biscrown-5 with and without alkali metal ions ($Na^+$, $K^+$, $Rb^+$, and $Cs^+$) have been theoretically investigated for the first time using molecular dynamic (MD) simulations and density functional theory (MPWB1K/6-31G(d)//B3LYP/6-31G(d)) methods. The formation of the metal ion complex by the host is mainly driven by the electrostatic attraction between crown-5 oxygens and a cation together with the minor contribution of the cation-$\pi$ interaction between two facing phenyl rings around the cation. The computed binding energies and the atomic charge distribution analysis for the metal binding complexes indicate the selectivity toward a potassium ion. The theoretical results herein explain the experimentally observed extractability order by this host towards various alkali metal ions. The physical nature and the driving forces for cation recognition by this host are discussed in detail.

• Journal of the Korea Institute of Building Construction
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• v.16 no.4
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• pp.321-329
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• 2016

The use of ternary blended cement consisting of Portland cement, granulated blast-furnace slag (GGBFS) and fly ash has been on the rise to improve marine concrete structure's resistance to chloride attack. Therefore, this study attempted to investigate changes in chloride attack resistibility of concrete through NT Build 492-based chloride migration experiments and test of concrete's ability to resist chloride ion penetration under ASTM C 1202(KS F 2271) when 1.5-2.0% of alkali-sulfate activator (modified alkali sulfate type) was added to the ternary blended cement mixtures (40% ordinary Portland cement + 40% GGBFS + 20% fly ash). Then, the results found the followings: Even though the slump for the plain concrete slightly declined depending on the use of the alkali-sulfate activator, compressive strength from day 2 to day 7 improved by 17-42%. In addition, the coefficient from non-steady-state migration experiments for the plain concrete measured at day 28 decreased by 36-56% depending on the use of alkali-sulfate. Furthermore, total charge passed according to the test for electrical indication of concrete's ability to resist chloride ion penetration decreased by 33-62% at day 7 and by 31-48% at day 28. As confirmed in previous studies, reactivity in the GGBFS and fly ash improved because of alkali activation. As a result, concrete strength increased due to reduced total porosity.

• Membrane Journal
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• v.30 no.4
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• pp.276-281
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• 2020

A research was conducted on the removal of ion from the solution involving the alkali metal ion and chlorine ion using ion exchange resin. The cation exchange resin and anion exchange resin was used for the remove of metal ion (Na⁺ and K⁺) and chlorine ion (Cl^-), respectively. In the case of solution A (involving 36,633 ppm of Na⁺ and 57,921 ppm of Cl^-), the Na⁺ ion and Cl^- ion were removed over 99% within 20 min. In the case of solution B (involving 1,638 ppm of K⁺), the K⁺ ion was removed over 99% within 3 min.

• Macromolecular Research
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• v.13 no.2
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• pp.141-146
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• 2005

Calix[4]crown-6-2,4-bis(4-aminobutyl ether), which has a crown-6 moiety at the 1,3-position and amino function at the 2,4-position, was prepared as an intermediate for the subsequent synthesis of calix[4]crown-6-containing polyamide and polyimide using adipoyl chloride and 1,2,4,5-benzenetetracarboxylic dianhydride. The chemical structures were characterized by IR, $^{1}H NMR$ spectroscopy and elemental analysis, and some of their physical properties, including their thermal behavior, were examined. The ion binding characteristics of the monomer and polymers for alkali metal and alkali earth metal ions were measured by liquid-liquid extraction from the aqueous phase into the organic phase. It has been observed that polyamide has a high binding ability towards various metal cations as compared to polyimide, which showed cesium ion selectivity.

• Computers and Concrete
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• v.12 no.4
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• pp.431-442
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• 2013

This study attempted to find a proper method applicable to simulating practical equifield lines of two-dimensional Accelerate Lithium Migration Technique (ALMT), and evaluate the feasibility of using the theoretical ion migration model of one-dimensional ALMT to predict the ion migration behavior of two-dimensional ALMT. The result showed that the electrolyte or carbon plate can be used as matrix to draw equifield line graph similar to that by using mortar as matrix. Using electrolyte electrode module for simulation has advantages of simple production, easy measurement, rapidness, and economy. The electrolyte module can be used to simulate the equifield line distribution diagram in practical two-dimensional electrode configuration firstly. Then, several equifield line zones were marked, and several subzones under one-dimensional ALMT were separated from various equifield line zones. The theoretical free content distribution of alkali in concrete under two-dimensional electric field effect could be obtained from duration analysis.

• Proceedings of the Korean Institute of Building Construction Conference
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• 2007.11a
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• pp.91-94
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• 2007

It is essential every concrete structure should continue to perform its intended functions, that is maintain its required strength and durability, during the service life. However, deterioration occurs more progressively from the outside of concrete exposed to severe conditions. Deterioration in the concrete structure is due to carbonation and chloride ion attack. Therefore, concrete structure is needed to surface protection for increase durability using impregnant. Impregnant classify into two large groups in polymeric and silicate materials. Silicate impregnant is included silane and alkali silicate(sodium and lithium silicate). Thus, this study is concerned with carbonation and chloride ion resistance of self cleaning hydrophilic impregnant of concrete structure using lithium and potassium silicate. From the experimental test result, lithium and potassium silicate have a good properties as a carbonation and chloride ion resistance. Lithium and potassium silicate make good use of hydrophilic impregnant.

• Journal of the Korean Institute of Illuminating and Electrical Installation Engineers
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• v.30 no.3
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• pp.59-64
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• 2016

Applications of electrolytic ion water generated by the oxidation-reduction have gradually been expanded due to their strong sterilizing power and a surface active force. We demonstrate the effect of the multi-layer type electrode for effective ion water generation. The multi-layer type electrode has ability to generate stronger acid and alkali water by increase of the electrode reactive area. Also power consumption efficiency enhances because the electrodes disposed in middle position of the reactive cell raise the usage rate by overlapped effect as an electrolysis electrode.